Condition | Indicated | Relationship Strength | Studies | Trials |
Coloboma Congenital anomaly in which some of the structures of the eye are absent due to incomplete fusion of the fetal intraocular fissure during gestation. | 0 | 8.88 | 103 | 0 |
Microphthalmia [description not available] | 0 | 9.49 | 176 | 0 |
Nearsightedness [description not available] | 0 | 23 | 1,058 | 29 |
Myopia A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness. | 0 | 23 | 1,058 | 29 |
2019 Novel Coronavirus Disease [description not available] | 0 | 11.6 | 105 | 0 |
Glaucoma An ocular disease, occurring in many forms, having as its primary characteristics an unstable or a sustained increase in the intraocular pressure which the eye cannot withstand without damage to its structure or impairment of its function. The consequences of the increased pressure may be manifested in a variety of symptoms, depending upon type and severity, such as excavation of the optic disk, hardness of the eyeball, corneal anesthesia, reduced visual acuity, seeing of colored halos around lights, disturbed dark adaptation, visual field defects, and headaches. (Dictionary of Visual Science, 4th ed) | 0 | 22.16 | 1,541 | 23 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 24.1 | 1,852 | 147 |
Cirrhosis [description not available] | 0 | 8.06 | 32 | 0 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 13.06 | 32 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 16.53 | 730 | 0 |
Uveitis Inflammation of part or all of the uvea, the middle (vascular) tunic of the eye, and commonly involving the other tunics (sclera and cornea, and the retina). (Dorland, 27th ed) | 0 | 16.76 | 454 | 2 |
Hereditary Autoinflammation Diseases [description not available] | 0 | 4.45 | 3 | 0 |
Autoimmune Disease [description not available] | 0 | 13.74 | 124 | 1 |
Eye Disorders [description not available] | 0 | 24.7 | 2,595 | 36 |
Autoimmune Diseases Disorders that are characterized by the production of antibodies that react with host tissues or immune effector cells that are autoreactive to endogenous peptides. | 0 | 18.74 | 124 | 1 |
Eye Diseases Diseases affecting the eye. | 0 | 24.7 | 2,595 | 36 |
Ocular Infections [description not available] | 0 | 8.91 | 66 | 0 |
Eye Infections Infection, moderate to severe, caused by bacteria, fungi, or viruses, which occurs either on the external surface of the eye or intraocularly with probable inflammation, visual impairment, or blindness. | 0 | 8.91 | 66 | 0 |
Onchocerciasis Infection with nematodes of the genus ONCHOCERCA. Characteristics include the presence of firm subcutaneous nodules filled with adult worms, PRURITUS, and ocular lesions. | 0 | 15.82 | 100 | 21 |
Retinal Pigment Epithelial Detachment [description not available] | 0 | 15.53 | 417 | 6 |
Syndrome, VKH (Vogt Koyanagi Harada) [description not available] | 0 | 6.27 | 19 | 0 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 5.08 | 10 | 0 |
Retinal Detachment Separation of the inner layers of the retina (neural retina) from the pigment epithelium. Retinal detachment occurs more commonly in men than in women, in eyes with degenerative myopia, in aging and in aphakia. It may occur after an uncomplicated cataract extraction, but it is seen more often if vitreous humor has been lost during surgery. (Dorland, 27th ed; Newell, Ophthalmology: Principles and Concepts, 7th ed, p310-12). | 0 | 15.53 | 417 | 6 |
Uveomeningoencephalitic Syndrome A syndrome characterized by bilateral granulomatous UVEITIS with IRITIS and secondary GLAUCOMA, premature ALOPECIA, symmetrical VITILIGO, poliosis circumscripta (a strand of depigmented hair), HEARING DISORDERS, and meningeal signs (neck stiffness and headache). Examination of the cerebrospinal fluid reveals a pattern consistent with MENINGITIS, ASEPTIC. (Adams et al., Principles of Neurology, 6th ed, p748; Surv Ophthalmol 1995 Jan;39(4):265-292) | 0 | 6.27 | 19 | 0 |
Lymphoma, Large B-Cell, Diffuse Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation. | 0 | 5.08 | 10 | 0 |
Choroid Hemorrhage Hemorrhage from the vessels of the choroid. | 0 | 3.42 | 7 | 0 |
Innate Inflammatory Response [description not available] | 0 | 17.07 | 368 | 6 |
Cat Diseases Diseases of the domestic cat (Felis catus or F. domesticus). This term does not include diseases of the so-called big cats such as CHEETAHS; LIONS; tigers, cougars, panthers, leopards, and other Felidae for which the heading CARNIVORA is used. | 0 | 10.61 | 62 | 3 |
Habronemiasis [description not available] | 0 | 6.14 | 28 | 1 |
Inflammation A pathological process characterized by injury or destruction of tissues caused by a variety of cytologic and chemical reactions. It is usually manifested by typical signs of pain, heat, redness, swelling, and loss of function. | 0 | 17.07 | 368 | 6 |
Argyria A permanent ashen-gray discoloration of the skin, conjunctiva, and internal organs resulting from long-continued use of silver salts. (Dorland, 27th ed) | 0 | 3.57 | 9 | 0 |
Exophthalmos Abnormal protrusion of both eyes; may be caused by endocrine gland malfunction, malignancy, injury, or paralysis of the extrinsic muscles of the eye. | 0 | 12.19 | 190 | 3 |
Bladder Cancer [description not available] | 0 | 5.39 | 5 | 1 |
Infectious Endophthalmitis Infectious condition of the internal eye. | 0 | 15.32 | 283 | 5 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 5.39 | 5 | 1 |
Endophthalmitis Suppurative inflammation of the tissues of the internal structures of the eye frequently associated with an infection. | 0 | 15.32 | 283 | 5 |
Afferent Pupillary Defect [description not available] | 0 | 6.39 | 26 | 0 |
Iris Diseases Diseases, dysfunctions, or disorders of or located in the iris. | 0 | 6.53 | 34 | 0 |
Fish Diseases Diseases of freshwater, marine, hatchery or aquarium fish. This term includes diseases of both teleosts (true fish) and elasmobranchs (sharks, rays and skates). | 0 | 6.97 | 69 | 1 |
Parasitic Diseases, Animal Animal diseases caused by PARASITES. | 0 | 3.8 | 11 | 0 |
Thyroid Diseases Pathological processes involving the THYROID GLAND. | 0 | 11.98 | 29 | 0 |
Retinal Dystrophies A group of disorders involving predominantly the posterior portion of the ocular fundus, due to degeneration in the sensory layer of the RETINA; RETINAL PIGMENT EPITHELIUM; BRUCH MEMBRANE; CHOROID; or a combination of these tissues. | 0 | 3.7 | 9 | 0 |
Diseases, Occupational [description not available] | 0 | 10.08 | 104 | 0 |
Glaucoma, Neovascular A form of secondary glaucoma which develops as a consequence of another ocular disease and is attributed to the forming of new vessels in the angle of the anterior chamber. | 0 | 13.64 | 41 | 9 |
Pseudophakia Presence of an intraocular lens after cataract extraction. | 0 | 13.31 | 37 | 2 |
Ataxia Impairment of the ability to perform smoothly coordinated voluntary movements. This condition may affect the limbs, trunk, eyes, pharynx, larynx, and other structures. Ataxia may result from impaired sensory or motor function. Sensory ataxia may result from posterior column injury or PERIPHERAL NERVE DISEASES. Motor ataxia may be associated with CEREBELLAR DISEASES; CEREBRAL CORTEX diseases; THALAMIC DISEASES; BASAL GANGLIA DISEASES; injury to the RED NUCLEUS; and other conditions. | 0 | 5.88 | 24 | 0 |
Cataract, Membranous [description not available] | 0 | 20.57 | 757 | 26 |
Polyneuropathy, Acquired [description not available] | 0 | 2.7 | 3 | 0 |
Pigmentary Retinopathy [description not available] | 0 | 8.99 | 65 | 1 |
Cataract Partial or complete opacity on or in the lens or capsule of one or both eyes, impairing vision or causing blindness. The many kinds of cataract are classified by their morphology (size, shape, location) or etiology (cause and time of occurrence). (Dorland, 27th ed) | 0 | 20.57 | 757 | 26 |
Polyneuropathies Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance. | 0 | 2.7 | 3 | 0 |
Retinitis Pigmentosa Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina. | 0 | 8.99 | 65 | 1 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 17.22 | 645 | 3 |
Ebola Hemorrhagic Fever [description not available] | 0 | 4.8 | 10 | 0 |
Hemorrhagic Fever, Ebola A highly fatal, acute hemorrhagic fever caused by EBOLAVIRUS. | 0 | 4.8 | 10 | 0 |
Amaurosis [description not available] | 0 | 18.31 | 356 | 0 |
Blindness The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; OPTIC CHIASM diseases; or BRAIN DISEASES affecting the VISUAL PATHWAYS or OCCIPITAL LOBE. | 0 | 13.31 | 356 | 0 |
Non-communicable Chronic Diseases [description not available] | 0 | 3.33 | 1 | 0 |
Blast Injuries Injuries resulting when a person is struck by particles impelled with violent force from an explosion. Blast causes pulmonary concussion and hemorrhage, laceration of other thoracic and abdominal viscera, ruptured ear drums, and minor effects in the central nervous system. (From Dorland, 27th ed) | 0 | 3.75 | 10 | 0 |
Diabetic Retinopathy Disease of the RETINA as a complication of DIABETES MELLITUS. It is characterized by the progressive microvascular complications, such as ANEURYSM, interretinal EDEMA, and intraocular PATHOLOGIC NEOVASCULARIZATION. | 0 | 25.4 | 596 | 298 |
Dry Eye [description not available] | 0 | 22.73 | 384 | 16 |
Dry Eye Syndromes Corneal and conjunctival dryness due to deficient tear production, predominantly in menopausal and post-menopausal women. Filamentary keratitis or erosion of the conjunctival and corneal epithelium may be caused by these disorders. Sensation of the presence of a foreign body in the eye and burning of the eyes may occur. | 0 | 22.73 | 384 | 16 |
Pulmonary Arterial Remodeling [description not available] | 0 | 3.23 | 1 | 0 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 10.16 | 42 | 2 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 7.28 | 24 | 0 |
Diabetes Mellitus, Type 2 A subclass of DIABETES MELLITUS that is not INSULIN-responsive or dependent (NIDDM). It is characterized initially by INSULIN RESISTANCE and HYPERINSULINEMIA; and eventually by GLUCOSE INTOLERANCE; HYPERGLYCEMIA; and overt diabetes. Type II diabetes mellitus is no longer considered a disease exclusively found in adults. Patients seldom develop KETOSIS but often exhibit OBESITY. | 0 | 10.16 | 42 | 2 |
Hypertrophy General increase in bulk of a part or organ due to CELL ENLARGEMENT and accumulation of FLUIDS AND SECRETIONS, not due to tumor formation, nor to an increase in the number of cells (HYPERPLASIA). | 0 | 13.42 | 44 | 2 |
Herpes Simplex Keratitis [description not available] | 0 | 6.95 | 50 | 0 |
Keratitis, Herpetic A superficial, epithelial Herpesvirus hominis infection of the cornea, characterized by the presence of small vesicles which may break down and coalesce to form dendritic ulcers (KERATITIS, DENDRITIC). (Dictionary of Visual Science, 3d ed) | 0 | 6.95 | 50 | 0 |
Bleb [description not available] | 0 | 4.77 | 12 | 0 |
Maggot Infestations [description not available] | 0 | 5.4 | 24 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 9.3 | 87 | 1 |
Viral Diseases [description not available] | 0 | 7.73 | 49 | 0 |
Herpes Simplex A group of acute infections caused by herpes simplex virus type 1 or type 2 that is characterized by the development of one or more small fluid-filled vesicles with a raised erythematous base on the skin or mucous membrane. It occurs as a primary infection or recurs due to a reactivation of a latent infection. (Dorland, 27th ed.) | 0 | 9.3 | 87 | 1 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 12.73 | 49 | 0 |
Chronic Primary Open Angle Glaucoma [description not available] | 0 | 17.75 | 283 | 41 |
Glaucoma, Open-Angle Glaucoma in which the angle of the anterior chamber is open and the trabecular meshwork does not encroach on the base of the iris. | 0 | 17.75 | 283 | 41 |
Central Retinal Edema, Cystoid [description not available] | 0 | 14.92 | 87 | 4 |
Macular Edema Fluid accumulation in the outer layer of the MACULA LUTEA that results from intraocular or systemic insults. It may develop in a diffuse pattern where the macula appears thickened or it may acquire the characteristic petaloid appearance referred to as cystoid macular edema. Although macular edema may be associated with various underlying conditions, it is most commonly seen following intraocular surgery, venous occlusive disease, DIABETIC RETINOPATHY, and posterior segment inflammatory disease. (From Survey of Ophthalmology 2004; 49(5) 470-90) | 0 | 14.92 | 87 | 4 |
Allergic Reaction [description not available] | 0 | 11.47 | 143 | 1 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 16.47 | 143 | 1 |
Keratoconus A noninflammatory, usually bilateral protrusion of the cornea, the apex being displaced downward and nasally. It occurs most commonly in females at about puberty. The cause is unknown but hereditary factors may play a role. The -conus refers to the cone shape of the corneal protrusion. (From Dorland, 27th ed) | 0 | 11.38 | 63 | 2 |
Neglected Diseases Diseases that are underfunded and have low name recognition but are major burdens in less developed countries. The World Health Organization has designated six tropical infectious diseases as being neglected in industrialized countries that are endemic in many developing countries (HELMINTHIASIS; LEPROSY; LYMPHATIC FILARIASIS; ONCHOCERCIASIS; SCHISTOSOMIASIS; and TRACHOMA). | 0 | 4.14 | 5 | 0 |
Infant, Newborn, Diseases Diseases of newborn infants present at birth (congenital) or developing within the first month of birth. It does not include hereditary diseases not manifesting at birth or within the first 30 days of life nor does it include inborn errors of metabolism. Both HEREDITARY DISEASES and METABOLISM, INBORN ERRORS are available as general concepts. | 0 | 6.35 | 40 | 0 |
Egyptian Ophthalmia [description not available] | 0 | 10.17 | 65 | 2 |
Amblyopia, Developmental [description not available] | 0 | 15.69 | 163 | 5 |
Amblyopia A nonspecific term referring to impaired vision. Major subcategories include stimulus deprivation-induced amblyopia and toxic amblyopia. Stimulus deprivation-induced amblyopia is a developmental disorder of the visual cortex. A discrepancy between visual information received by the visual cortex from each eye results in abnormal cortical development. STRABISMUS and REFRACTIVE ERRORS may cause this condition. Toxic amblyopia is a disorder of the OPTIC NERVE which is associated with ALCOHOLISM, tobacco SMOKING, and other toxins and as an adverse effect of the use of some medications. | 0 | 15.69 | 163 | 5 |
Injuries, Radiation [description not available] | 0 | 19.62 | 265 | 29 |
Atypical Hemolytic-Uremic Syndrome [description not available] | 0 | 3.82 | 3 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura [description not available] | 0 | 3.59 | 3 | 0 |
Purpura, Thrombotic Thrombocytopenic An acquired, congenital, or familial disorder caused by PLATELET AGGREGATION with THROMBOSIS in terminal arterioles and capillaries. Clinical features include THROMBOCYTOPENIA; HEMOLYTIC ANEMIA; AZOTEMIA; FEVER; and thrombotic microangiopathy. The classical form also includes neurological symptoms and end-organ damage, such as RENAL FAILURE. Mutations in the ADAMTS13 PROTEIN gene have been identified in familial cases. | 0 | 3.59 | 3 | 0 |
Thrombotic Microangiopathies Diseases that result in THROMBOSIS in MICROVASCULATURE. The two most prominent diseases are PURPURA, THROMBOTIC THROMBOCYTOPENIC; and HEMOLYTIC-UREMIC SYNDROME. Multiple etiological factors include VASCULAR ENDOTHELIAL CELL damage due to SHIGA TOXIN; FACTOR H deficiency; and aberrant VON WILLEBRAND FACTOR formation. | 0 | 3.6 | 2 | 0 |
Atypical Hemolytic Uremic Syndrome An hereditary hemolytic uremic syndrome associated with variations in the gene that encodes COMPLEMENT FACTOR H, or the related proteins CFHR1 and CFHR3. Disease often progresses to CHRONIC KIDNEY FAILURE without the prodromal symptoms of ENTEROCOLITIS and DIARRHEA that characterize typical hemolytic uremic syndrome. | 0 | 3.82 | 3 | 0 |
Palmoplantaris Pustulosis [description not available] | 0 | 7.03 | 17 | 0 |
Psoriasis A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. | 0 | 7.03 | 17 | 0 |
Retinal Diseases Diseases involving the RETINA. | 0 | 18.46 | 344 | 13 |
Angiogenesis, Pathologic [description not available] | 0 | 16.02 | 263 | 2 |
Cancer of Eye [description not available] | 0 | 15.61 | 469 | 3 |
Day Blindness [description not available] | 0 | 19.95 | 404 | 26 |
Alopecia Cicatrisata [description not available] | 0 | 4.22 | 18 | 0 |
Abnormalities, Skin [description not available] | 0 | 2.38 | 2 | 0 |
Chondrodysplasia Punctata A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC), an autosomal dominant form (Conradi-Hunermann syndrome), and a milder X-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form. | 0 | 2.89 | 4 | 0 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 9.22 | 18 | 0 |
Skin Abnormalities Congenital structural abnormalities of the skin. | 0 | 2.38 | 2 | 0 |
Diseases of Endocrine System [description not available] | 0 | 5.54 | 9 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 5.54 | 9 | 0 |
Koch's Disease [description not available] | 0 | 8.49 | 351 | 0 |
Ocular Tuberculosis [description not available] | 0 | 14.35 | 290 | 0 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 8.49 | 351 | 0 |
Anterior Optic Neuritis [description not available] | 0 | 11.18 | 157 | 1 |
Choked Disk [description not available] | 0 | 10.77 | 154 | 1 |
Optic Neuritis Inflammation of the optic nerve. Commonly associated conditions include autoimmune disorders such as MULTIPLE SCLEROSIS, infections, and granulomatous diseases. Clinical features include retro-orbital pain that is aggravated by eye movement, loss of color vision, and contrast sensitivity that may progress to severe visual loss, an afferent pupillary defect (Marcus-Gunn pupil), and in some instances optic disc hyperemia and swelling. Inflammation may occur in the portion of the nerve within the globe (neuropapillitis or anterior optic neuritis) or the portion behind the globe (retrobulbar neuritis or posterior optic neuritis). | 0 | 11.18 | 157 | 1 |
Papilledema Swelling of the OPTIC DISK, usually in association with increased intracranial pressure, characterized by hyperemia, blurring of the disk margins, microhemorrhages, blind spot enlargement, and engorgement of retinal veins. Chronic papilledema may cause OPTIC ATROPHY and visual loss. (Miller et al., Clinical Neuro-Ophthalmology, 4th ed, p175) | 0 | 15.77 | 154 | 1 |
Canine Diseases [description not available] | 0 | 12.02 | 146 | 4 |
Uveitis, Anterior Inflammation of the anterior uvea comprising the iris, angle structures, and the ciliary body. Manifestations of this disorder include ciliary injection, exudation into the anterior chamber, iris changes, and adhesions between the iris and lens (posterior synechiae). Intraocular pressure may be increased or reduced. | 0 | 7.64 | 56 | 0 |
Apoplexy [description not available] | 0 | 13.66 | 35 | 1 |
Cerebral Ischemia [description not available] | 0 | 7.11 | 38 | 0 |
Branch Retinal Artery Occlusion [description not available] | 0 | 10.04 | 48 | 2 |
Brain Ischemia Localized reduction of blood flow to brain tissue due to arterial obstruction or systemic hypoperfusion. This frequently occurs in conjunction with brain hypoxia (HYPOXIA, BRAIN). Prolonged ischemia is associated with BRAIN INFARCTION. | 0 | 7.11 | 38 | 0 |
Retinal Artery Occlusion Sudden ISCHEMIA in the RETINA due to blocked blood flow through the CENTRAL RETINAL ARTERY or its branches leading to sudden complete or partial loss of vision, respectively, in the eye. | 0 | 15.04 | 48 | 2 |
Stroke A group of pathological conditions characterized by sudden, non-convulsive loss of neurological function due to BRAIN ISCHEMIA or INTRACRANIAL HEMORRHAGES. Stroke is classified by the type of tissue NECROSIS, such as the anatomic location, vasculature involved, etiology, age of the affected individual, and hemorrhagic vs. non-hemorrhagic nature. (From Adams et al., Principles of Neurology, 6th ed, pp777-810) | 0 | 8.66 | 35 | 1 |
Anasarca [description not available] | 0 | 22.05 | 395 | 291 |
Bilateral Headache [description not available] | 0 | 12.99 | 96 | 7 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 22.05 | 395 | 291 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 12.99 | 96 | 7 |
Auricular Fibrillation [description not available] | 0 | 8.97 | 5 | 0 |
Blood Pressure, High [description not available] | 0 | 13.4 | 230 | 3 |
Atrial Fibrillation Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation. | 0 | 3.97 | 5 | 0 |
Hypertension Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more. | 0 | 13.4 | 230 | 3 |
Skin Aging The process of aging due to changes in the structure and elasticity of the skin over time. It may be a part of physiological aging or it may be due to the effects of ultraviolet radiation, usually through exposure to sunlight. | 0 | 16.27 | 90 | 32 |
Concomitant Strabismus [description not available] | 0 | 14.89 | 343 | 7 |
Strabismus Misalignment of the visual axes of the eyes. In comitant strabismus the degree of ocular misalignment does not vary with the direction of gaze. In noncomitant strabismus the degree of misalignment varies depending on direction of gaze or which eye is fixating on the target. (Miller, Walsh & Hoyt's Clinical Neuro-Ophthalmology, 4th ed, p641) | 0 | 14.89 | 343 | 7 |
Pink Eye [description not available] | 0 | 13.25 | 161 | 4 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 13.25 | 161 | 4 |
Sicca Syndrome [description not available] | 0 | 9.08 | 28 | 2 |
Carotid Artery Narrowing [description not available] | 0 | 9.76 | 87 | 1 |
Ischemia A hypoperfusion of the BLOOD through an organ or tissue caused by a PATHOLOGIC CONSTRICTION or obstruction of its BLOOD VESSELS, or an absence of BLOOD CIRCULATION. | 0 | 13.96 | 318 | 1 |
Sjogren's Syndrome Chronic inflammatory and autoimmune disease in which the salivary and lacrimal glands undergo progressive destruction by lymphocytes and plasma cells resulting in decreased production of saliva and tears. The primary form, often called sicca syndrome, involves both KERATOCONJUNCTIVITIS SICCA and XEROSTOMIA. The secondary form includes, in addition, the presence of a connective tissue disease, usually rheumatoid arthritis. | 0 | 9.08 | 28 | 2 |
Carotid Stenosis Narrowing or stricture of any part of the CAROTID ARTERIES, most often due to atherosclerotic plaque formation. Ulcerations may form in atherosclerotic plaques and induce THROMBUS formation. Platelet or cholesterol emboli may arise from stenotic carotid lesions and induce a TRANSIENT ISCHEMIC ATTACK; CEREBROVASCULAR ACCIDENT; or temporary blindness (AMAUROSIS FUGAX). (From Adams et al., Principles of Neurology, 6th ed, pp 822-3) | 0 | 14.76 | 87 | 1 |
Active Hyperemia [description not available] | 0 | 11.67 | 65 | 16 |
C-C Fistula [description not available] | 0 | 7.24 | 51 | 0 |
Hyperemia The presence of an increased amount of blood in a body part or an organ leading to congestion or engorgement of blood vessels. Hyperemia can be due to increase of blood flow into the area (active or arterial), or due to obstruction of outflow of blood from the area (passive or venous). | 0 | 16.67 | 65 | 16 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 17.12 | 561 | 2 |
Disease Exacerbation [description not available] | 0 | 18.95 | 242 | 10 |
Autoimmune Diabetes [description not available] | 0 | 9.16 | 36 | 2 |
Diabetes Mellitus, Type 1 A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence. | 0 | 9.16 | 36 | 2 |
Keratitis Inflammation of the cornea. | 0 | 13.94 | 205 | 2 |
Eczema, Atopic [description not available] | 0 | 5.88 | 16 | 0 |
Dermatitis, Atopic A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. | 0 | 5.88 | 16 | 0 |
Diffuse Lymphocytic Lymphoma, Poorly-Differentiated [description not available] | 0 | 2.85 | 3 | 0 |
Lymphoma, Mantle-Cell A form of non-Hodgkin lymphoma having a usually diffuse pattern with both small and medium lymphocytes and small cleaved cells. It accounts for about 5% of adult non-Hodgkin lymphomas in the United States and Europe. The majority of mantle-cell lymphomas are associated with a t(11;14) translocation resulting in overexpression of the CYCLIN D1 gene (GENES, BCL-1). | 0 | 2.85 | 3 | 0 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 11.62 | 53 | 3 |
6th Nerve Palsy [description not available] | 0 | 3.5 | 8 | 0 |
Nerve Pain [description not available] | 0 | 5.58 | 11 | 0 |
Injuries, Spinal Cord [description not available] | 0 | 2.93 | 4 | 0 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 5.58 | 11 | 0 |
Spinal Cord Injuries Penetrating and non-penetrating injuries to the spinal cord resulting from traumatic external forces (e.g., WOUNDS, GUNSHOT; WHIPLASH INJURIES; etc.). | 0 | 2.93 | 4 | 0 |
Chronic Illness [description not available] | 0 | 15.76 | 148 | 10 |
Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). | 0 | 20.76 | 148 | 10 |
Lacerations Torn, ragged, mangled wounds. | 0 | 3.22 | 6 | 0 |
HbS Disease [description not available] | 0 | 6.17 | 18 | 0 |
Albinism, Tyrosinase-Negative [description not available] | 0 | 5.29 | 12 | 0 |
Anemia, Sickle Cell A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. | 0 | 6.17 | 18 | 0 |
Albinism, Oculocutaneous Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types. | 0 | 5.29 | 12 | 0 |
Benign Mucosal Pemphigoid [description not available] | 0 | 6.01 | 15 | 0 |
Pemphigoid [description not available] | 0 | 9.5 | 5 | 0 |
Pemphigoid, Benign Mucous Membrane A chronic blistering disease with predilection for mucous membranes and less frequently the skin, and with a tendency to scarring. It is sometimes called ocular pemphigoid because of conjunctival mucous membrane involvement. | 0 | 6.01 | 15 | 0 |
Pemphigoid, Bullous A chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. | 0 | 4.5 | 5 | 0 |
Convergent Strabismus [description not available] | 0 | 9.26 | 67 | 2 |
Alternating Exotropia [description not available] | 0 | 6.98 | 28 | 1 |
Esotropia A form of ocular misalignment characterized by an excessive convergence of the visual axes, resulting in a cross-eye appearance. An example of this condition occurs when paralysis of the lateral rectus muscle causes an abnormal inward deviation of one eye on attempted gaze. | 0 | 9.26 | 67 | 2 |
Blastomycosis, North American [description not available] | 0 | 4.38 | 8 | 0 |
Blastomycosis A fungal infection that may appear in two forms: 1, a primary lesion characterized by the formation of a small cutaneous nodule and small nodules along the lymphatics that may heal within several months; and 2, chronic granulomatous lesions characterized by thick crusts, warty growths, and unusual vascularity and infection in the middle or upper lobes of the lung. | 0 | 4.38 | 8 | 0 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 7.85 | 30 | 0 |
Bacterial Eye Infections [description not available] | 0 | 12.7 | 93 | 3 |
Uveitis, Sympathetic [description not available] | 0 | 4.78 | 33 | 0 |
Eye Injuries, Penetrating Deeply perforating or puncturing type intraocular injuries. | 0 | 8.18 | 61 | 1 |
Ophthalmia, Sympathetic Granulomatous uveitis which follows in one eye after a penetrating injury to the other eye; the secondarily affected eye is called the sympathizing eye, and the injured eye is called the exciting or activating eye. | 0 | 4.78 | 33 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 7.46 | 21 | 1 |
Ischemic Attack, Transient Brief reversible episodes of focal, nonconvulsive ischemic dysfunction of the brain having a duration of less than 24 hours, and usually less than one hour, caused by transient thrombotic or embolic blood vessel occlusion or stenosis. Events may be classified by arterial distribution, temporal pattern, or etiology (e.g., embolic vs. thrombotic). (From Adams et al., Principles of Neurology, 6th ed, pp814-6) | 0 | 7.46 | 21 | 1 |
Bacteremia The presence of viable bacteria circulating in the blood. Fever, chills, tachycardia, and tachypnea are common acute manifestations of bacteremia. The majority of cases are seen in already hospitalized patients, most of whom have underlying diseases or procedures which render their bloodstreams susceptible to invasion. | 0 | 3.13 | 5 | 0 |
B-Cell Lymphoma [description not available] | 0 | 4.47 | 8 | 0 |
T-Cell Lymphoma [description not available] | 0 | 2.82 | 3 | 0 |
Lymphoma, B-Cell A group of heterogeneous lymphoid tumors generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes. | 0 | 4.47 | 8 | 0 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 2.82 | 3 | 0 |
Autism [description not available] | 0 | 13.71 | 79 | 2 |
Autistic Disorder A disorder beginning in childhood. It is marked by the presence of markedly abnormal or impaired development in social interaction and communication and a markedly restricted repertoire of activity and interest. Manifestations of the disorder vary greatly depending on the developmental level and chronological age of the individual. (DSM-V) | 0 | 13.71 | 79 | 2 |
Diplopia A visual symptom in which a single object is perceived by the visual cortex as two objects rather than one. Disorders associated with this condition include REFRACTIVE ERRORS; STRABISMUS; OCULOMOTOR NERVE DISEASES; TROCHLEAR NERVE DISEASES; ABDUCENS NERVE DISEASES; and diseases of the BRAIN STEM and OCCIPITAL LOBE. | 0 | 8.22 | 70 | 0 |
B. burgdorferi Infection [description not available] | 0 | 4.46 | 8 | 0 |
Lyme Disease An infectious disease caused by a spirochete, BORRELIA BURGDORFERI, which is transmitted chiefly by Ixodes dammini (see IXODES) and pacificus ticks in the United States and Ixodes ricinis (see IXODES) in Europe. It is a disease with early and late cutaneous manifestations plus involvement of the nervous system, heart, eye, and joints in variable combinations. The disease was formerly known as Lyme arthritis and first discovered at Old Lyme, Connecticut. | 0 | 4.46 | 8 | 0 |
Graft-Versus-Host Disease [description not available] | 0 | 11.69 | 35 | 3 |
Graft vs Host Disease The clinical entity characterized by anorexia, diarrhea, loss of hair, leukopenia, thrombocytopenia, growth retardation, and eventual death brought about by the GRAFT VS HOST REACTION. | 0 | 11.69 | 35 | 3 |
Besnier-Boeck Disease [description not available] | 0 | 8.61 | 72 | 0 |
Sarcoidosis An idiopathic systemic inflammatory granulomatous disorder comprised of epithelioid and multinucleated giant cells with little necrosis. It usually invades the lungs with fibrosis and may also involve lymph nodes, skin, liver, spleen, eyes, phalangeal bones, and parotid glands. | 0 | 8.61 | 72 | 0 |
Age-Related Macular Degeneration [description not available] | 0 | 17.98 | 253 | 8 |
Macular Degeneration Degenerative changes in the RETINA usually of older adults which results in a loss of vision in the center of the visual field (the MACULA LUTEA) because of damage to the retina. It occurs in dry and wet forms. | 0 | 17.98 | 253 | 8 |
Franceschetti-Zwahlen-Klein Syndrome [description not available] | 0 | 3.9 | 13 | 0 |
Ametropia [description not available] | 0 | 17.62 | 452 | 10 |
Refractive Errors Deviations from the average or standard indices of refraction of the eye through its dioptric or refractive apparatus. | 0 | 17.62 | 452 | 10 |
Elevated ICP (Intracranial Pressure) [description not available] | 0 | 6.44 | 42 | 1 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 3.41 | 6 | 0 |
Intracranial Hypertension Increased pressure within the cranial vault. This may result from several conditions, including HYDROCEPHALUS; BRAIN EDEMA; intracranial masses; severe systemic HYPERTENSION; PSEUDOTUMOR CEREBRI; and other disorders. | 0 | 6.44 | 42 | 1 |
Infarction, Middle Cerebral Artery NECROSIS occurring in the MIDDLE CEREBRAL ARTERY distribution system which brings blood to the entire lateral aspects of each CEREBRAL HEMISPHERE. Clinical signs include impaired cognition; APHASIA; AGRAPHIA; weak and numbness in the face and arms, contralaterally or bilaterally depending on the infarction. | 0 | 3.41 | 6 | 0 |
Hereditary Hemorrhagic Telangiectasia [description not available] | 0 | 5.14 | 11 | 0 |
Telangiectasia, Hereditary Hemorrhagic An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA. | 0 | 5.14 | 11 | 0 |
Progressive Tapetochoroidal Dystrophy [description not available] | 0 | 4.31 | 3 | 0 |
Choroideremia An X chromosome-linked abnormality characterized by atrophy of the choroid and degeneration of the retinal pigment epithelium causing night blindness. | 0 | 4.31 | 3 | 0 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 6.34 | 28 | 0 |
Adult Optic Nerve Glioma [description not available] | 0 | 3.51 | 8 | 0 |
Neurofibromatosis 1 An autosomal dominant inherited disorder (with a high frequency of spontaneous mutations) that features developmental changes in the nervous system, muscles, bones, and skin, most notably in tissue derived from the embryonic NEURAL CREST. Multiple hyperpigmented skin lesions and subcutaneous tumors are the hallmark of this disease. Peripheral and central nervous system neoplasms occur frequently, especially OPTIC NERVE GLIOMA and NEUROFIBROSARCOMA. NF1 is caused by mutations which inactivate the NF1 gene (GENES, NEUROFIBROMATOSIS 1) on chromosome 17q. The incidence of learning disabilities is also elevated in this condition. (From Adams et al., Principles of Neurology, 6th ed, pp1014-18) There is overlap of clinical features with NOONAN SYNDROME in a syndrome called neurofibromatosis-Noonan syndrome. Both the PTPN11 and NF1 gene products are involved in the SIGNAL TRANSDUCTION pathway of Ras (RAS PROTEINS). | 0 | 6.34 | 28 | 0 |
Optic Nerve Glioma Glial cell derived tumors arising from the optic nerve, usually presenting in childhood. | 0 | 3.51 | 8 | 0 |
Complications of Diabetes Mellitus [description not available] | 0 | 13.45 | 109 | 1 |
Choroid Neovascularization [description not available] | 0 | 12.17 | 71 | 2 |
Neovascularization, Optic Disc [description not available] | 0 | 10.07 | 42 | 1 |
Retinal Neovascularization Formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina. | 0 | 10.07 | 42 | 1 |
Wet Macular Degeneration A form of RETINAL DEGENERATION in which abnormal CHOROIDAL NEOVASCULARIZATION occurs under the RETINA and MACULA LUTEA, causing bleeding and leaking of fluid. This leads to bulging and or lifting of the macula and the distortion or destruction of central vision. | 0 | 3.66 | 8 | 0 |
Malignant Melanoma [description not available] | 0 | 13.82 | 236 | 5 |
Benign Neoplasms [description not available] | 0 | 14.54 | 308 | 1 |
Melanoma A malignant neoplasm derived from cells that are capable of forming melanin, which may occur in the skin of any part of the body, in the eye, or, rarely, in the mucous membranes of the genitalia, anus, oral cavity, or other sites. It occurs mostly in adults and may originate de novo or from a pigmented nevus or malignant lentigo. Melanomas frequently metastasize widely, and the regional lymph nodes, liver, lungs, and brain are likely to be involved. The incidence of malignant skin melanomas is rising rapidly in all parts of the world. (Stedman, 25th ed; from Rook et al., Textbook of Dermatology, 4th ed, p2445) | 0 | 13.82 | 236 | 5 |
Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. | 0 | 19.54 | 308 | 1 |
Cystic Periventricular Leukomalacia [description not available] | 0 | 2.44 | 2 | 0 |
Leukomalacia, Periventricular Degeneration of white matter adjacent to the CEREBRAL VENTRICLES following cerebral hypoxia or BRAIN ISCHEMIA in neonates. The condition primarily affects white matter in the perfusion zone between superficial and deep branches of the MIDDLE CEREBRAL ARTERY. Clinical manifestations include VISION DISORDERS; CEREBRAL PALSY; PARAPLEGIA; SEIZURES; and cognitive disorders. (From Adams et al., Principles of Neurology, 6th ed, p1021; Joynt, Clinical Neurology, 1997, Ch4, pp30-1) | 0 | 2.44 | 2 | 0 |
Retrolental Fibroplasia [description not available] | 0 | 14.29 | 110 | 9 |
Retinopathy of Prematurity A bilateral retinopathy occurring in premature infants treated with excessively high concentrations of oxygen, characterized by vascular dilatation, proliferation, and tortuosity, edema, and retinal detachment, with ultimate conversion of the retina into a fibrous mass that can be seen as a dense retrolental membrane. Usually growth of the eye is arrested and may result in microophthalmia, and blindness may occur. (Dorland, 27th ed) | 0 | 14.29 | 110 | 9 |
Gout Metabolic disorder characterized by recurrent acute arthritis, hyperuricemia and deposition of sodium urate in and around the joints, sometimes with formation of URIC ACID calculi. | 0 | 3.04 | 5 | 0 |
Aortitis Syndrome [description not available] | 0 | 5.07 | 17 | 0 |
Takayasu Arteritis A chronic inflammatory process that affects the AORTA and its primary branches, such as the brachiocephalic artery (BRACHIOCEPHALIC TRUNK) and CAROTID ARTERIES. It results in progressive arterial stenosis, occlusion, and aneurysm formation. The pulse in the arm is hard to detect. Patients with aortitis syndrome often exhibit retinopathy. | 0 | 10.07 | 17 | 0 |
Complication, Postoperative [description not available] | 0 | 16.66 | 302 | 17 |
Postoperative Complications Pathologic processes that affect patients after a surgical procedure. They may or may not be related to the disease for which the surgery was done, and they may or may not be direct results of the surgery. | 0 | 16.66 | 302 | 17 |
Anophthalmia [description not available] | 0 | 7.79 | 79 | 0 |
Cyst [description not available] | 0 | 9.13 | 77 | 1 |
Autism Spectrum Disorder Wide continuum of associated cognitive and neurobehavioral disorders, including, but not limited to, three core-defining features: impairments in socialization, impairments in verbal and nonverbal communication, and restricted and repetitive patterns of behaviors. (from DSM-V) | 0 | 7.24 | 18 | 0 |
Glaucoma, Suspect [description not available] | 0 | 20.6 | 155 | 22 |
Ocular Hypertension A condition in which the intraocular pressure is elevated above normal and which may lead to glaucoma. | 0 | 15.6 | 155 | 22 |
Leukoma [description not available] | 0 | 9.61 | 104 | 1 |
Cockayne-Touraine Disease [description not available] | 0 | 2.9 | 2 | 0 |
Corneal Opacity Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque. | 0 | 9.61 | 104 | 1 |
Epidermolysis Bullosa Dystrophica Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS. | 0 | 2.9 | 2 | 0 |
Branch Vein Occlusion [description not available] | 0 | 11.68 | 83 | 2 |
Retinal Vein Occlusion Blockage of the RETINAL VEIN. Those at high risk for this condition include patients with HYPERTENSION; DIABETES MELLITUS; ATHEROSCLEROSIS; and other CARDIOVASCULAR DISEASES. | 0 | 11.68 | 83 | 2 |
Presbyopia The normal decreasing elasticity of the crystalline lens that leads to loss of accommodation. | 0 | 6.87 | 37 | 0 |
Farsightedness [description not available] | 0 | 15.27 | 231 | 3 |
Hyperopia A refractive error in which rays of light entering the eye parallel to the optic axis are brought to a focus behind the retina, as a result of the eyeball being too short from front to back. It is also called farsightedness because the near point is more distant than it is in emmetropia with an equal amplitude of accommodation. (Dorland, 27th ed) | 0 | 15.27 | 231 | 3 |
Atherogenesis [description not available] | 0 | 4.77 | 7 | 0 |
Atherosclerosis A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. | 0 | 4.77 | 7 | 0 |
Acute Coronary Syndrome An episode of MYOCARDIAL ISCHEMIA that generally lasts longer than a transient anginal episode that ultimately may lead to MYOCARDIAL INFARCTION. | 0 | 2.41 | 1 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 6.19 | 21 | 0 |
Cystic Echinococcosis [description not available] | 0 | 4.16 | 6 | 0 |
Congestive Ophthalmopathy [description not available] | 0 | 11.11 | 69 | 6 |
Graves Ophthalmopathy An autoimmune disorder of the EYE, occurring in patients with Graves disease. Subtypes include congestive (inflammation of the orbital connective tissue), myopathic (swelling and dysfunction of the extraocular muscles), and mixed congestive-myopathic ophthalmopathy. | 0 | 16.11 | 69 | 6 |
Congenital Infection, Toxoplasma gondii [description not available] | 0 | 4.65 | 29 | 0 |
Ocular Toxoplasmosis [description not available] | 0 | 12.9 | 109 | 0 |
Toxoplasmosis, Congenital Prenatal protozoal infection with TOXOPLASMA gondii which is associated with injury to the developing fetal nervous system. The severity of this condition is related to the stage of pregnancy during which the infection occurs; first trimester infections are associated with a greater degree of neurologic dysfunction. Clinical features include HYDROCEPHALUS; MICROCEPHALY; deafness; cerebral calcifications; SEIZURES; and psychomotor retardation. Signs of a systemic infection may also be present at birth, including fever, rash, and hepatosplenomegaly. (From Adams et al., Principles of Neurology, 6th ed, p735) | 0 | 4.65 | 29 | 0 |
Toxoplasmosis, Ocular Infection caused by the protozoan parasite TOXOPLASMA in which there is extensive connective tissue proliferation, the retina surrounding the lesions remains normal, and the ocular media remain clear. Chorioretinitis may be associated with all forms of toxoplasmosis, but is usually a late sequel of congenital toxoplasmosis. The severe ocular lesions in infants may lead to blindness. | 0 | 7.9 | 109 | 0 |
Achromatopsia Severely deficient color perception, typically with monochromacy and reduced visual acuity. The atypical form can include normal visual acuity with pseudomonochromacy. | 0 | 7.22 | 38 | 1 |
Color Vision Defects Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue. | 0 | 7.22 | 38 | 1 |
Cranial Nerve II Injuries [description not available] | 0 | 8.47 | 46 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 5.93 | 4 | 1 |
Vitamin D Deficiency A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406) | 0 | 5.93 | 4 | 1 |
Hereditary Optic Neuroretinopathy [description not available] | 0 | 7.39 | 15 | 0 |
Optic Atrophy, Hereditary, Leber A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001)) | 0 | 7.39 | 15 | 0 |
Symptom Cluster [description not available] | 0 | 11.73 | 293 | 0 |
Syndrome A characteristic symptom complex. | 0 | 11.73 | 293 | 0 |
Extravascular Hemolysis [description not available] | 0 | 5.66 | 31 | 0 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 5.66 | 31 | 0 |
Sensitivity and Specificity Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed) | 0 | 17.12 | 219 | 6 |
Cancer of the Retina [description not available] | 0 | 8.48 | 56 | 1 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 11.86 | 145 | 4 |
Retinoblastoma A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104) | 0 | 11.86 | 145 | 4 |
Mydriasis Dilation of pupils to greater than 6 mm combined with failure of the pupils to constrict when stimulated with light. This condition may occur due to injury of the pupillary fibers in the oculomotor nerve, in acute angle-closure glaucoma, and in ADIE SYNDROME. | 0 | 11.98 | 18 | 1 |
Cytomegaloviral Retinitis [description not available] | 0 | 7.73 | 23 | 3 |
Dyskeratosis Congenita, X-Linked [description not available] | 0 | 2.6 | 1 | 0 |
Cytomegalovirus A genus of the family HERPESVIRIDAE, subfamily BETAHERPESVIRINAE, infecting the salivary glands, liver, spleen, lungs, eyes, and other organs, in which they produce characteristically enlarged cells with intranuclear inclusions. Infection with Cytomegalovirus is also seen as an opportunistic infection in AIDS. | 0 | 8.52 | 39 | 1 |
Cytomegalovirus Retinitis Infection of the retina by cytomegalovirus characterized by retinal necrosis, hemorrhage, vessel sheathing, and retinal edema. Cytomegalovirus retinitis is a major opportunistic infection in AIDS patients and can cause blindness. | 0 | 12.73 | 23 | 3 |
Dyskeratosis Congenita A predominantly X-linked recessive syndrome characterized by a triad of reticular skin pigmentation, nail dystrophy and leukoplakia of mucous membranes. Oral and dental abnormalities may also be present. Complications are a predisposition to malignancy and bone marrow involvement with pancytopenia. (from Int J Paediatr Dent 2000 Dec;10(4):328-34) The X-linked form is also known as Zinsser-Cole-Engman syndrome and involves the gene which encodes a highly conserved protein called dyskerin. | 0 | 2.6 | 1 | 0 |
Acne Rosacea [description not available] | 0 | 5.95 | 16 | 0 |
Rosacea A cutaneous disorder primarily of convexities of the central part of the FACE, such as FOREHEAD; CHEEK; NOSE; and CHIN. It is characterized by FLUSHING; ERYTHEMA; EDEMA; RHINOPHYMA; papules; and ocular symptoms. It may occur at any age but typically after age 30. There are various subtypes of rosacea: erythematotelangiectatic, papulopustular, phymatous, and ocular (National Rosacea Society's Expert Committee on the Classification and Staging of Rosacea, J Am Acad Dermatol 2002; 46:584-7). | 0 | 10.95 | 16 | 0 |
Infections, Neisseriaceae [description not available] | 0 | 2.47 | 2 | 0 |
Bacterial Conjunctivitides [description not available] | 0 | 8.14 | 26 | 1 |
Conjunctivitis, Bacterial Purulent infections of the conjunctiva by several species of gram-negative, gram-positive, or acid-fast organisms. Some of the more commonly found genera causing conjunctival infections are Haemophilus, Streptococcus, Neisseria, and Chlamydia. | 0 | 8.14 | 26 | 1 |
Hypertensive Retinopathy Degenerative changes to the RETINA due to HYPERTENSION. | 0 | 5.12 | 6 | 0 |
Congenital Nystagmus [description not available] | 0 | 8.53 | 8 | 0 |
Congenital Zika Syndrome [description not available] | 0 | 6.28 | 11 | 0 |
Complications, Infectious Pregnancy [description not available] | 0 | 9.8 | 38 | 1 |
Zika Virus Infection A viral disease transmitted by the bite of AEDES mosquitoes infected with ZIKA VIRUS. Its mild DENGUE-like symptoms include fever, rash, headaches and ARTHRALGIA. The viral infection during pregnancy, in rare cases, is associated with congenital brain and ocular abnormalities, called Congenital Zika Syndrome, including MICROCEPHALY and may also lead to GUILLAIN-BARRE SYNDROME. | 0 | 11.28 | 11 | 0 |
Ectopia Lentis Congenital displacement of the lens resulting from defective zonule formation. | 0 | 9 | 13 | 0 |
Fuch's Endothelial Dystrophy [description not available] | 0 | 4.34 | 4 | 0 |
Fuchs' Endothelial Dystrophy Disorder caused by loss of endothelium of the central cornea. It is characterized by hyaline endothelial outgrowths on Descemet's membrane, epithelial blisters, reduced vision, and pain. | 0 | 4.34 | 4 | 0 |
Cranial Nerve IV Diseases [description not available] | 0 | 3.55 | 7 | 0 |
Palsy [description not available] | 0 | 8.44 | 133 | 1 |
Paralysis A general term most often used to describe severe or complete loss of muscle strength due to motor system disease from the level of the cerebral cortex to the muscle fiber. This term may also occasionally refer to a loss of sensory function. (From Adams et al., Principles of Neurology, 6th ed, p45) | 0 | 8.44 | 133 | 1 |
Cancer of Ovary [description not available] | 0 | 3.86 | 4 | 0 |
Ovarian Neoplasms Tumors or cancer of the OVARY. These neoplasms can be benign or malignant. They are classified according to the tissue of origin, such as the surface EPITHELIUM, the stromal endocrine cells, and the totipotent GERM CELLS. | 0 | 3.86 | 4 | 0 |
Ocular Toxicity [description not available] | 0 | 5.78 | 8 | 0 |
Germinoblastoma [description not available] | 0 | 7.43 | 26 | 0 |
Central Nervous System Neoplasm [description not available] | 0 | 4.48 | 8 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 7.43 | 26 | 0 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 4.48 | 8 | 0 |
Lassitude [description not available] | 0 | 5.71 | 33 | 0 |
Fatigue The state of weariness following a period of exertion, mental or physical, characterized by a decreased capacity for work and reduced efficiency to respond to stimuli. | 0 | 5.71 | 33 | 0 |
Corneal Diseases Diseases of the cornea. | 0 | 12.48 | 118 | 1 |
Genetic Predisposition [description not available] | 0 | 10.15 | 67 | 0 |
Allergic Conjunctivitis [description not available] | 0 | 13.69 | 86 | 7 |
Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | 0 | 13.69 | 86 | 7 |
Keratoconjunctivitis Simultaneous inflammation of the cornea and conjunctiva. | 0 | 10.72 | 82 | 2 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 5.74 | 10 | 0 |
Acute Lymphoid Leukemia [description not available] | 0 | 6.86 | 17 | 0 |
Precursor Cell Lymphoblastic Leukemia-Lymphoma A neoplasm characterized by abnormalities of the lymphoid cell precursors leading to excessive lymphoblasts in the marrow and other organs. It is the most common cancer in children and accounts for the vast majority of all childhood leukemias. | 0 | 6.86 | 17 | 0 |
Rubeola [description not available] | 0 | 4.03 | 15 | 0 |
Neuroretinitis [description not available] | 0 | 9.77 | 107 | 1 |
Encephalitis, Inclusion Body, Measles [description not available] | 0 | 2.71 | 3 | 0 |
Measles A highly contagious infectious disease caused by MORBILLIVIRUS, common among children but also seen in the nonimmune of any age, in which the virus enters the respiratory tract via droplet nuclei and multiplies in the epithelial cells, spreading throughout the MONONUCLEAR PHAGOCYTE SYSTEM. | 0 | 4.03 | 15 | 0 |
Retinitis Inflammation of the RETINA. It is rarely limited to the retina, but is commonly associated with diseases of the choroid (CHORIORETINITIS) and of the OPTIC DISK (neuroretinitis). | 0 | 9.77 | 107 | 1 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 11.51 | 219 | 1 |
Electrolytes Substances that dissociate into two or more ions, to some extent, in water. Solutions of electrolytes thus conduct an electric current and can be decomposed by it (ELECTROLYSIS). (Grant & Hackh's Chemical Dictionary, 5th ed) | 0 | 6.81 | 15 | 1 |
Herpes Zoster, Ocular [description not available] | 0 | 7.18 | 43 | 0 |
Herpes Zoster Ophthalmicus Virus infection of the Gasserian ganglion and its nerve branches characterized by pain and vesicular eruptions with much swelling. Ocular involvement is usually heralded by a vesicle on the tip of the nose. This area is innervated by the nasociliary nerve. | 0 | 12.18 | 43 | 0 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 4.71 | 31 | 0 |
Neisseria gonorrhoeae Infection [description not available] | 0 | 11.54 | 18 | 1 |
Gonorrhea Acute infectious disease characterized by primary invasion of the urogenital tract. The etiologic agent, NEISSERIA GONORRHOEAE, was isolated by Neisser in 1879. | 0 | 6.54 | 18 | 1 |
Vascular Diseases Pathological processes involving any of the BLOOD VESSELS in the cardiac or peripheral circulation. They include diseases of ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 9.07 | 104 | 0 |
Drug-Induced Stevens Johnson Syndrome [description not available] | 0 | 7.9 | 40 | 0 |
Stevens-Johnson Syndrome Rare cutaneous eruption characterized by extensive KERATINOCYTE apoptosis resulting in skin detachment with mucosal involvement. It is often provoked by the use of drugs (e.g., antibiotics and anticonvulsants) or associated with PNEUMONIA, MYCOPLASMA. It is considered a continuum of Toxic Epidermal Necrolysis. | 0 | 12.9 | 40 | 0 |
Keratitis, Ulcerative [description not available] | 0 | 8.76 | 80 | 0 |
Corneal Perforation A puncture or hole through the CORNEAL STROMA resulting from various diseases or trauma. | 0 | 3.99 | 4 | 0 |
Corneal Ulcer Loss of epithelial tissue from the surface of the cornea due to progressive erosion and necrosis of the tissue; usually caused by bacterial, fungal, or viral infection. | 0 | 13.76 | 80 | 0 |
Eye Abnormalities Congenital absence of or defects in structures of the eye; may also be hereditary. | 0 | 12.22 | 476 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 6 | 27 | 0 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 6 | 27 | 0 |
Bladder Pain Syndrome [description not available] | 0 | 3.33 | 1 | 0 |
Bladder, Overactive [description not available] | 0 | 5.73 | 3 | 2 |
Cystitis, Interstitial A condition with recurring discomfort or pain in the URINARY BLADDER and the surrounding pelvic region without an identifiable disease. Severity of pain in interstitial cystitis varies greatly and often is accompanied by increased urination frequency and urgency. | 0 | 3.33 | 1 | 0 |
Urinary Bladder, Overactive Symptom of overactive detrusor muscle of the URINARY BLADDER that contracts with abnormally high frequency and urgency. Overactive bladder is characterized by the frequent feeling of needing to urinate during the day, during the night, or both. URINARY INCONTINENCE may or may not be present. | 0 | 5.73 | 3 | 2 |
Constriction, Pathological [description not available] | 0 | 7.86 | 32 | 1 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 7.86 | 32 | 1 |
Chalazia [description not available] | 0 | 2.37 | 2 | 0 |
Chalazion A non-neoplastic cyst of the MEIBOMIAN GLANDS of the eyelid. | 0 | 2.37 | 2 | 0 |
Dermoid [description not available] | 0 | 4.95 | 15 | 0 |
Dysembryoma [description not available] | 0 | 3.9 | 13 | 0 |
Teratoma A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642) | 0 | 3.9 | 13 | 0 |
Gnathostoma Infection [description not available] | 0 | 3.28 | 2 | 0 |
Injuries, Eye [description not available] | 0 | 15.65 | 483 | 5 |
Wounds, Gunshot Disruption of structural continuity of the body as a result of the discharge of firearms. | 0 | 3.68 | 10 | 0 |
Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | 0 | 15.65 | 483 | 5 |
ANCA-Associated Vasculitides [description not available] | 0 | 3.73 | 3 | 0 |
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis Group of systemic vasculitis with a strong association with ANCA. The disorders are characterized by necrotizing inflammation of small and medium size vessels, with little or no immune-complex deposits in vessel walls. | 0 | 3.73 | 3 | 0 |
MS (Multiple Sclerosis) [description not available] | 0 | 7.62 | 81 | 0 |
Multiple Sclerosis An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903) | 0 | 7.62 | 81 | 0 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 4.25 | 7 | 0 |
Ache [description not available] | 0 | 15.13 | 135 | 19 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 15.13 | 135 | 19 |
Acute Ischemic Stroke [description not available] | 0 | 2.41 | 1 | 0 |
Ischemic Stroke Stroke due to BRAIN ISCHEMIA resulting in interruption or reduction of blood flow to a part of the brain. When obstruction is due to a BLOOD CLOT formed within in a cerebral blood vessel it is a thrombotic stroke. When obstruction is formed elsewhere and moved to block a cerebral blood vessel (see CEREBRAL EMBOLISM) it is referred to as embolic stroke. Wake-up stroke refers to ischemic stroke occurring during sleep while cryptogenic stroke refers to ischemic stroke of unknown origin. | 0 | 2.41 | 1 | 0 |
Equine Diseases [description not available] | 0 | 10.39 | 66 | 2 |
IgG4 Related Systemic Disease [description not available] | 0 | 2.82 | 2 | 0 |
Granuloma, Plasma Cell, Orbital [description not available] | 0 | 5.12 | 10 | 0 |
Immunoglobulin G4-Related Disease A spectrum of systemic autoimmune diseases in which IMMUNOGLOBULIN G4 plays a pathophysiologic role. It can affect multiple organs in highly variable presentations, characterized by inflammatory lesions composed of IgG4-positive PLASMA CELLS, further infiltrated by T helper cells (T-LYMPHOCYTES, HELPER-INDUCER) when linked to progressive FIBROSIS and eventual organ damage. | 0 | 2.82 | 2 | 0 |
Orbital Pseudotumor A nonspecific tumor-like inflammatory lesion in the ORBIT of the eye. It is usually composed of mature LYMPHOCYTES; PLASMA CELLS; MACROPHAGES; LEUKOCYTES with varying degrees of FIBROSIS. Orbital pseudotumors are often associated with inflammation of the extraocular muscles (ORBITAL MYOSITIS) or inflammation of the lacrimal glands (DACRYOADENITIS). | 0 | 5.12 | 10 | 0 |
Orbital Diseases Diseases of the bony orbit and contents except the eyeball. | 0 | 9.16 | 87 | 0 |
Alopecia Circumscripta [description not available] | 0 | 2.71 | 3 | 0 |
Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | 0 | 2.71 | 3 | 0 |
Ptosis, Eyelid [description not available] | 0 | 9.86 | 52 | 3 |
Chronic Progressive External Ophthalmoplegia with Myopathy [description not available] | 0 | 2.98 | 4 | 0 |
External Ophthalmoplegia [description not available] | 0 | 12.93 | 113 | 0 |
Blepharoptosis Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle. | 0 | 9.86 | 52 | 3 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 6.04 | 16 | 0 |
Hypoglycemia A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH. | 0 | 6.04 | 16 | 0 |
Dry Macular Degeneration [description not available] | 0 | 5.53 | 9 | 0 |
Geographic Atrophy A form of MACULAR DEGENERATION also known as dry macular degeneration marked by occurrence of a well-defined progressive lesion or atrophy in the central part of the RETINA called the MACULA LUTEA. It is distinguishable from WET MACULAR DEGENERATION in that the latter involves neovascular exudates. | 0 | 5.53 | 9 | 0 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 7.64 | 108 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 3.26 | 6 | 0 |
Leukemia, Lymphocytic, Chronic, B-Cell A chronic leukemia characterized by abnormal B-lymphocytes and often generalized lymphadenopathy. In patients presenting predominately with blood and bone marrow involvement it is called chronic lymphocytic leukemia (CLL); in those predominately with enlarged lymph nodes it is called small lymphocytic lymphoma. These terms represent spectrums of the same disease. | 0 | 3.26 | 6 | 0 |
Macular Holes [description not available] | 0 | 8.95 | 50 | 1 |
Retinal Perforations Perforations through the whole thickness of the retina including the macula as the result of inflammation, trauma, degeneration, etc. The concept includes retinal breaks, tears, dialyses, and holes. | 0 | 8.95 | 50 | 1 |
Corneal Dystrophies [description not available] | 0 | 6.98 | 25 | 0 |
Acrocephaly Premature closing of the lambdoid and coronal sutures. | 0 | 5.19 | 19 | 0 |
Craniofacial Dysarthrosis [description not available] | 0 | 5.33 | 22 | 0 |
Craniosynostoses Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes associated with congenital syndromes such as ACROCEPHALOSYNDACTYLIA; and CRANIOFACIAL DYSOSTOSIS. | 0 | 5.19 | 19 | 0 |
Adult-Onset Vitelliform Macular Dystrophy [description not available] | 0 | 2.84 | 3 | 0 |
Acantholysis Bullosa [description not available] | 0 | 3.05 | 5 | 0 |
Parodontosis [description not available] | 0 | 3.42 | 2 | 0 |
Actinic Reticuloid Syndrome [description not available] | 0 | 7.79 | 30 | 1 |
Epidermolysis Bullosa Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties. | 0 | 8.05 | 5 | 0 |
Periodontal Diseases Pathological processes involving the PERIODONTIUM including the gum (GINGIVA), the alveolar bone (ALVEOLAR PROCESS), the DENTAL CEMENTUM, and the PERIODONTAL LIGAMENT. | 0 | 3.42 | 2 | 0 |
Dirofilariasis Infection with nematodes of the genus DIROFILARIA, usually in animals, especially dogs, but occasionally in man. | 0 | 8.6 | 9 | 0 |
alpha-Dystroglycanopathies [description not available] | 0 | 3.04 | 4 | 0 |
Collodion Baby Syndrome [description not available] | 0 | 2.7 | 3 | 0 |
Eye Infections, Viral Infections of the eye caused by minute intracellular agents. These infections may lead to severe inflammation in various parts of the eye - conjunctiva, iris, eyelids, etc. Several viruses have been identified as the causative agents. Among these are Herpesvirus, Adenovirus, Poxvirus, and Myxovirus. | 0 | 7.82 | 36 | 0 |
Ichthyosis, Lamellar A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds within a few weeks. Scaling is generalized and marked with grayish-brown quadrilateral scales, adherent at their centers and free at the edges. In some cases, scales are so thick that they resemble armored plate. | 0 | 2.7 | 3 | 0 |
Cystine Diathesis [description not available] | 0 | 5.82 | 23 | 0 |
Cystinosis A metabolic disease characterized by the defective transport of CYSTINE across the lysosomal membrane due to mutation of a membrane protein cystinosin. This results in cystine accumulation and crystallization in the cells causing widespread tissue damage. In the KIDNEY, nephropathic cystinosis is a common cause of RENAL FANCONI SYNDROME. | 0 | 5.82 | 23 | 0 |
Pemphigus Foliaceus [description not available] | 0 | 5.21 | 12 | 0 |
Episcleritis [description not available] | 0 | 6.81 | 28 | 0 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 10.21 | 12 | 0 |
Scleritis Refers to any inflammation of the sclera including episcleritis, a benign condition affecting only the episclera, which is generally short-lived and easily treated. Classic scleritis, on the other hand, affects deeper tissue and is characterized by higher rates of visual acuity loss and even mortality, particularly in necrotizing form. Its characteristic symptom is severe and general head pain. Scleritis has also been associated with systemic collagen disease. Etiology is unknown but is thought to involve a local immune response. Treatment is difficult and includes administration of anti-inflammatory and immunosuppressive agents such as corticosteroids. Inflammation of the sclera may also be secondary to inflammation of adjacent tissues, such as the conjunctiva. | 0 | 6.81 | 28 | 0 |
Hansen Disease [description not available] | 0 | 5.36 | 60 | 0 |
Leprosy A chronic granulomatous infection caused by MYCOBACTERIUM LEPRAE. The granulomatous lesions are manifested in the skin, the mucous membranes, and the peripheral nerves. Two polar or principal types are lepromatous and tuberculoid. | 0 | 5.36 | 60 | 0 |
Klein Syndrome [description not available] | 0 | 3.99 | 14 | 0 |
Histoplasma capsulatum Infection [description not available] | 0 | 5.35 | 23 | 0 |
Cerebral Nocardiosis [description not available] | 0 | 4.65 | 10 | 0 |
Histoplasmosis Infection resulting from exposure to the fungus HISTOPLASMA. It is worldwide in distribution and particularly common in the central and eastern states, especially areas around the Ohio and Mississippi River valleys. | 0 | 5.35 | 23 | 0 |
Co-infection [description not available] | 0 | 4.4 | 6 | 0 |
Adenoma Sebaceum Facial ANGIOFIBROMA in tuberous sclerosis | 0 | 6.01 | 28 | 0 |
Tuberous Sclerosis Autosomal dominant neurocutaneous syndrome classically characterized by MENTAL RETARDATION; EPILEPSY; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). There is, however, considerable heterogeneity in the neurologic manifestations. It is also associated with cortical tuber and HAMARTOMAS formation throughout the body, especially the heart, kidneys, and eyes. Mutations in two loci TSC1 and TSC2 that encode hamartin and tuberin, respectively, are associated with the disease. | 0 | 11.01 | 28 | 0 |
Vision, Diminished [description not available] | 0 | 7.36 | 43 | 0 |
Idiopathic Parkinson Disease [description not available] | 0 | 9.76 | 30 | 2 |
Parkinson Disease A progressive, degenerative neurologic disease characterized by a TREMOR that is maximal at rest, retropulsion (i.e. a tendency to fall backwards), rigidity, stooped posture, slowness of voluntary movements, and a masklike facial expression. Pathologic features include loss of melanin containing neurons in the substantia nigra and other pigmented nuclei of the brainstem. LEWY BODIES are present in the substantia nigra and locus coeruleus but may also be found in a related condition (LEWY BODY DISEASE, DIFFUSE) characterized by dementia in combination with varying degrees of parkinsonism. (Adams et al., Principles of Neurology, 6th ed, p1059, pp1067-75) | 0 | 9.76 | 30 | 2 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 3.98 | 5 | 0 |
Granulomatosis, Lipid [description not available] | 0 | 3.52 | 1 | 0 |
Histiocytosis, Langerhans-Cell A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder. | 0 | 3.98 | 5 | 0 |
Erdheim-Chester Disease A rare form of non-Langerhans-cell histiocytosis (HISTIOCYTOSIS, NON-LANGERHANS-CELL) with onset in middle age. The systemic disease is characterized by infiltration of lipid-laden macrophages, multinucleated giant cells, an inflammatory infiltrate of lymphocytes and histiocytes in the bone marrow, and a generalized sclerosis of the long bones. | 0 | 3.52 | 1 | 0 |
Anterior Ischemic Optic Neuropathy [description not available] | 0 | 7.93 | 40 | 0 |
Optic Neuropathy, Ischemic Ischemic injury to the OPTIC NERVE which usually affects the OPTIC DISK (optic neuropathy, anterior ischemic) and less frequently the retrobulbar portion of the nerve (optic neuropathy, posterior ischemic). The injury results from occlusion of arterial blood supply which may result from TEMPORAL ARTERITIS; ATHEROSCLEROSIS; COLLAGEN DISEASES; EMBOLISM; DIABETES MELLITUS; and other conditions. The disease primarily occurs in the sixth decade or later and presents with the sudden onset of painless and usually severe monocular visual loss. Anterior ischemic optic neuropathy also features optic disk edema with microhemorrhages. The optic disk appears normal in posterior ischemic optic neuropathy. (Glaser, Neuro-Ophthalmology, 2nd ed, p135) | 0 | 7.93 | 40 | 0 |
Nephrotic Syndrome A condition characterized by severe PROTEINURIA, greater than 3.5 g/day in an average adult. The substantial loss of protein in the urine results in complications such as HYPOPROTEINEMIA; generalized EDEMA; HYPERTENSION; and HYPERLIPIDEMIAS. Diseases associated with nephrotic syndrome generally cause chronic kidney dysfunction. | 0 | 2.91 | 4 | 0 |
Myopia, Pathological [description not available] | 0 | 6.98 | 30 | 0 |
Sclera Diseases [description not available] | 0 | 5.77 | 21 | 0 |
Myopia, Degenerative Excessive axial myopia associated with complications (especially posterior staphyloma and CHOROIDAL NEOVASCULARIZATION) that can lead to BLINDNESS. | 0 | 6.98 | 30 | 0 |
Eye Infections, Parasitic Mild to severe infections of the eye and its adjacent structures (adnexa) by adult or larval protozoan or metazoan parasites. | 0 | 7.3 | 55 | 0 |
Muscular Weakness [description not available] | 0 | 4.74 | 12 | 0 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 6.32 | 39 | 0 |
Myasthenia Gravis A disorder of neuromuscular transmission characterized by fatigable weakness of cranial and skeletal muscles with elevated titers of ACETYLCHOLINE RECEPTORS or muscle-specific receptor tyrosine kinase (MuSK) autoantibodies. Clinical manifestations may include ocular muscle weakness (fluctuating, asymmetric, external ophthalmoplegia; diplopia; ptosis; and weakness of eye closure) and extraocular fatigable weakness of facial, bulbar, respiratory, and proximal limb muscles. The disease may remain limited to the ocular muscles (ocular myasthenia). THYMOMA is commonly associated with this condition. | 0 | 6.32 | 39 | 0 |
Muscle Weakness A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251) | 0 | 9.74 | 12 | 0 |
Hermanski-Pudlak Syndrome Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin. | 0 | 3.43 | 7 | 0 |
Cerebromeningitis [description not available] | 0 | 5.01 | 16 | 0 |
Conjugate Nystagmus [description not available] | 0 | 8.81 | 89 | 0 |
Craniofacial Abnormalities Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones. | 0 | 5.47 | 25 | 0 |
Absence of Corpus Callosum [description not available] | 0 | 3.29 | 6 | 0 |
HIV Coinfection [description not available] | 0 | 8.46 | 35 | 1 |
HIV Infections Includes the spectrum of human immunodeficiency virus infections that range from asymptomatic seropositivity, thru AIDS-related complex (ARC), to acquired immunodeficiency syndrome (AIDS). | 0 | 8.46 | 35 | 1 |
Coenuri Infection [description not available] | 0 | 6.05 | 29 | 0 |
Cysticercosis Infection with CYSTICERCUS, the larval form of the various tapeworms of the genus Taenia (usually T. solium in man). In humans they penetrate the intestinal wall and invade subcutaneous tissue, brain, eye, muscle, heart, liver, lung, and peritoneum. Brain involvement results in NEUROCYSTICERCOSIS. | 0 | 6.05 | 29 | 0 |
Blepharitis Inflammation of the eyelids. | 0 | 8.75 | 24 | 1 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 7.94 | 22 | 1 |
Cancer of Skin [description not available] | 0 | 9.23 | 86 | 0 |
Local Neoplasm Recurrence [description not available] | 0 | 7.81 | 37 | 2 |
Carcinoma, Basal Cell A malignant skin neoplasm that seldom metastasizes but has potentialities for local invasion and destruction. Clinically it is divided into types: nodular, cicatricial, morphaic, and erythematoid (pagetoid). They develop on hair-bearing skin, most commonly on sun-exposed areas. Approximately 85% are found on the head and neck area and the remaining 15% on the trunk and limbs. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1471) | 0 | 7.94 | 22 | 1 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 9.23 | 86 | 0 |
Eye Pain A dull or sharp painful sensation associated with the outer or inner structures of the eyeball, having different causes. | 0 | 8.95 | 23 | 1 |
Marfan Syndrome, Type I [description not available] | 0 | 7.89 | 34 | 0 |
Marfan Syndrome An autosomal dominant disorder of CONNECTIVE TISSUE with abnormal features in the heart, the eye, and the skeleton. Cardiovascular manifestations include MITRAL VALVE PROLAPSE, dilation of the AORTA, and aortic dissection. Other features include lens displacement (ectopia lentis), disproportioned long limbs and enlarged DURA MATER (dural ectasia). Marfan syndrome (type 1) is associated with mutations in the gene encoding FIBRILLIN-1 (FBN1), a major element of extracellular microfibrils of connective tissue. Mutations in the gene encoding TYPE II TGF-BETA RECEPTOR (TGFBR2) are associated with Marfan syndrome type 2. | 0 | 7.89 | 34 | 0 |
Blunt Injuries [description not available] | 0 | 6.51 | 32 | 0 |
Blow Out Fracture [description not available] | 0 | 6.62 | 36 | 0 |
Fractures, Multiple Injuries involving the breaking of either several bones or one bone in two or more places. | 0 | 2.41 | 1 | 0 |
Autokinetic Effect [description not available] | 0 | 5.13 | 18 | 0 |
Aortic Incompetence [description not available] | 0 | 2.88 | 3 | 0 |
Aortic Valve Insufficiency Pathological condition characterized by the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to regurgitation. It is caused by diseases of the AORTIC VALVE or its surrounding tissue (aortic root). | 0 | 2.88 | 3 | 0 |
Cardiomyopathy, Hypertrophic Obstructive [description not available] | 0 | 2.6 | 1 | 0 |
Familial Turner Syndrome [description not available] | 0 | 2.53 | 2 | 0 |
Cardiomyopathy, Hypertrophic A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY). | 0 | 2.6 | 1 | 0 |
Noonan Syndrome A genetically heterogeneous, multifaceted disorder characterized by short stature, webbed neck, ptosis, skeletal malformations, hypertelorism, hormonal imbalance, CRYPTORCHIDISM, multiple cardiac abnormalities (most commonly including PULMONARY VALVE STENOSIS), and some degree of INTELLECTUAL DISABILITY. The phenotype bears similarities to that of TURNER SYNDROME that occurs only in females and has its basis in a 45, X karyotype abnormality. Noonan syndrome occurs in both males and females with a normal karyotype (46,XX and 46,XY). Mutations in a several genes (PTPN11, KRAS, SOS1, NF1 and RAF1) have been associated the NS phenotype. Mutations in PTPN11 are the most common. LEOPARD SYNDROME, a disorder that has clinical features overlapping those of Noonan Syndrome, is also due to mutations in PTPN11. In addition, there is overlap with the syndrome called neurofibromatosis-Noonan syndrome due to mutations in NF1. | 0 | 2.53 | 2 | 0 |
Itching [description not available] | 0 | 9.81 | 21 | 3 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 0 | 14.81 | 21 | 3 |
Uveitis, Posterior Inflammation of the choroid as well as the retina and vitreous body. Some form of visual disturbance is usually present. The most important characteristics of posterior uveitis are vitreous opacities, choroiditis, and chorioretinitis. | 0 | 4.82 | 5 | 0 |
Surgical Incision [description not available] | 0 | 5.09 | 5 | 1 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 3.95 | 14 | 0 |
Light Sensitivity [description not available] | 0 | 4.09 | 16 | 0 |
Exanthem [description not available] | 0 | 7.38 | 20 | 0 |
Exanthema Diseases in which skin eruptions or rashes are a prominent manifestation. Classically, six such diseases were described with similar rashes; they were numbered in the order in which they were reported. Only the fourth (Duke's disease), fifth (ERYTHEMA INFECTIOSUM), and sixth (EXANTHEMA SUBITUM) numeric designations survive as occasional synonyms in current terminology. | 0 | 7.38 | 20 | 0 |
Cranial Nerve II Diseases [description not available] | 0 | 18.78 | 557 | 17 |
Optic Nerve Diseases Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect. | 0 | 18.78 | 557 | 17 |
Apnea, Obstructive Sleep [description not available] | 0 | 3.68 | 3 | 0 |
Sleep Apnea, Obstructive A disorder characterized by recurrent apneas during sleep despite persistent respiratory efforts. It is due to upper airway obstruction. The respiratory pauses may induce HYPERCAPNIA or HYPOXIA. Cardiac arrhythmias and elevation of systemic and pulmonary arterial pressures may occur. Frequent partial arousals occur throughout sleep, resulting in relative SLEEP DEPRIVATION and daytime tiredness. Associated conditions include OBESITY; ACROMEGALY; MYXEDEMA; micrognathia; MYOTONIC DYSTROPHY; adenotonsilar dystrophy; and NEUROMUSCULAR DISEASES. (From Adams et al., Principles of Neurology, 6th ed, p395) | 0 | 3.68 | 3 | 0 |
Muscle Contraction A process leading to shortening and/or development of tension in muscle tissue. Muscle contraction occurs by a sliding filament mechanism whereby actin filaments slide inward among the myosin filaments. | 0 | 15.16 | 40 | 3 |
Encephalopathy, Traumatic [description not available] | 0 | 3.23 | 4 | 0 |
Cranial Nerve III Diseases [description not available] | 0 | 4.16 | 6 | 0 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 3.23 | 4 | 0 |
Cerebellar Diseases Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. | 0 | 4.88 | 14 | 0 |
Adamantiades-Behcet Disease [description not available] | 0 | 8.98 | 54 | 0 |
Behcet Syndrome Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well. | 0 | 8.98 | 54 | 0 |
Dermatoses [description not available] | 0 | 8.11 | 81 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 8.11 | 81 | 0 |
Acute Idiopathic Blind Spot Enlargement Syndrome [description not available] | 0 | 3.64 | 2 | 0 |
Rodent Diseases Diseases of rodents of the order RODENTIA. This term includes diseases of Sciuridae (squirrels), Geomyidae (gophers), Heteromyidae (pouched mice), Castoridae (beavers), Cricetidae (rats and mice), Muridae (Old World rats and mice), Erethizontidae (porcupines), and Caviidae (guinea pigs). | 0 | 6.28 | 26 | 0 |
Brachial Paresis [description not available] | 0 | 3.96 | 14 | 0 |
Corneal Angiogenesis [description not available] | 0 | 7.68 | 19 | 1 |
Corneal Neovascularization New blood vessels originating from the corneal blood vessels and extending from the limbus into the adjacent CORNEAL STROMA. Neovascularization in the superficial and/or deep corneal stroma is a sequel to numerous inflammatory diseases of the ocular anterior segment, such as TRACHOMA, viral interstitial KERATITIS, microbial KERATOCONJUNCTIVITIS, and the immune response elicited by CORNEAL TRANSPLANTATION. | 0 | 7.68 | 19 | 1 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 9.57 | 39 | 3 |
Panophthalmitis Acute suppurative inflammation of the inner eye with necrosis of the sclera (and sometimes the cornea) and extension of the inflammation into the orbit. Pain may be severe and the globe may rupture. In endophthalmitis the globe does not rupture. | 0 | 6.41 | 30 | 0 |
Breathlessness [description not available] | 0 | 3.12 | 5 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 3.12 | 5 | 0 |
Adverse Drug Event [description not available] | 0 | 9.37 | 73 | 0 |
Drug-Related Side Effects and Adverse Reactions Disorders that result from the intended use of PHARMACEUTICAL PREPARATIONS. Included in this heading are a broad variety of chemically-induced adverse conditions due to toxicity, DRUG INTERACTIONS, and metabolic effects of pharmaceuticals. | 0 | 9.37 | 73 | 0 |
Acute Disease Disease having a short and relatively severe course. | 0 | 12.98 | 119 | 4 |
Sporothrix brasiliensis Infection [description not available] | 0 | 3.22 | 6 | 0 |
Sporotrichosis The commonest and least serious of the deep mycoses, characterized by nodular lesions of the cutaneous and subcutaneous tissues. It is caused by inhalation of contaminated dust or by infection of a wound with SPOROTHRIX. | 0 | 3.22 | 6 | 0 |
Glaucoma, Angle Closure [description not available] | 0 | 7.62 | 80 | 0 |
Glaucoma, Angle-Closure A form of glaucoma in which the intraocular pressure increases because the angle of the anterior chamber is blocked and the aqueous humor cannot drain from the anterior chamber. | 0 | 7.62 | 80 | 0 |
Alastrim [description not available] | 0 | 3.04 | 5 | 0 |
Smallpox An acute, highly contagious, often fatal infectious disease caused by an orthopoxvirus characterized by a biphasic febrile course and distinctive progressive skin eruptions. Vaccination has succeeded in eradicating smallpox worldwide. (Dorland, 28th ed) | 0 | 8.04 | 5 | 0 |
Encephalopathy, Toxic [description not available] | 0 | 4.76 | 11 | 0 |
Cornea Injuries [description not available] | 0 | 6.93 | 32 | 0 |
Corneal Injuries Damage or trauma inflicted to the CORNEA by external means. | 0 | 6.93 | 32 | 0 |
Basedow Disease [description not available] | 0 | 12.74 | 118 | 7 |
Graves Disease A common form of hyperthyroidism with a diffuse hyperplastic GOITER. It is an autoimmune disorder that produces antibodies against the THYROID STIMULATING HORMONE RECEPTOR. These autoantibodies activate the TSH receptor, thereby stimulating the THYROID GLAND and hypersecretion of THYROID HORMONES. These autoantibodies can also affect the eyes (GRAVES OPHTHALMOPATHY) and the skin (Graves dermopathy). | 0 | 12.74 | 118 | 7 |
Kaposi Sarcoma [description not available] | 0 | 5.17 | 18 | 0 |
Sarcoma, Kaposi A multicentric, malignant neoplastic vascular proliferation characterized by the development of bluish-red cutaneous nodules, usually on the lower extremities, most often on the toes or feet, and slowly increasing in size and number and spreading to more proximal areas. The tumors have endothelium-lined channels and vascular spaces admixed with variably sized aggregates of spindle-shaped cells, and often remain confined to the skin and subcutaneous tissue, but widespread visceral involvement may occur. Kaposi's sarcoma occurs spontaneously in Jewish and Italian males in Europe and the United States. An aggressive variant in young children is endemic in some areas of Africa. A third form occurs in about 0.04% of kidney transplant patients. There is also a high incidence in AIDS patients. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, pp2105-7) HHV-8 is the suspected cause. | 0 | 5.17 | 18 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 8.08 | 54 | 0 |
Amentia [description not available] | 0 | 5.28 | 20 | 0 |
Alzheimer Disease A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57) | 0 | 8.08 | 54 | 0 |
Dementia An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness. | 0 | 5.28 | 20 | 0 |
Mucositis An INFLAMMATION of the MUCOSA with burning or tingling sensation. It is characterized by atrophy of the squamous EPITHELIUM, vascular damage, inflammatory infiltration, and ulceration. It usually occurs at the mucous lining of the MOUTH, the GASTROINTESTINAL TRACT or the airway due to chemical irritations, CHEMOTHERAPY, or radiation therapy (RADIOTHERAPY). | 0 | 6.93 | 10 | 0 |
Bacterial Disease [description not available] | 0 | 11.09 | 71 | 2 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 16.09 | 71 | 2 |
Acute Relapsing Multiple Sclerosis [description not available] | 0 | 4.21 | 13 | 0 |
Multiple Sclerosis, Relapsing-Remitting The most common clinical variant of MULTIPLE SCLEROSIS, characterized by recurrent acute exacerbations of neurologic dysfunction followed by partial or complete recovery. Common clinical manifestations include loss of visual (see OPTIC NEURITIS), motor, sensory, or bladder function. Acute episodes of demyelination may occur at any site in the central nervous system, and commonly involve the optic nerves, spinal cord, brain stem, and cerebellum. (Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 4.21 | 13 | 0 |
Anisometropia A condition of an inequality of refractive power of the two eyes. | 0 | 10.39 | 61 | 0 |
Astigmatism Unequal curvature of the refractive surfaces of the eye. Thus a point source of light cannot be brought to a point focus on the retina but is spread over a more or less diffuse area. This results from the radius of curvature in one plane being longer or shorter than the radius at right angles to it. (Dorland, 27th ed) | 0 | 10.71 | 123 | 1 |
Mucorales Infection [description not available] | 0 | 7.56 | 23 | 1 |
Mucormycosis Infection in humans and animals caused by any fungus in the order MUCORALES (e.g., RHIZOPUS; MUCOR; CUNNINGHAMELLA; APOPHYSOMYCES; ABSIDIA; SAKSENAEA and RHIZOMUCOR) There are many clinical types associated with infection including central nervous system, lung, gastrointestinal tract, skin, orbit and paranasal sinuses. In humans, it usually occurs as an OPPORTUNISTIC INFECTION. | 0 | 7.56 | 23 | 1 |
Facial Hemiatrophy A syndrome characterized by slowly progressive unilateral atrophy of facial subcutaneous fat, muscle tissue, skin, cartilage, and bone. The condition typically progresses over a period of 2-10 years and then stabilizes. | 0 | 3.75 | 11 | 0 |
Dermatosclerosis [description not available] | 0 | 3.67 | 10 | 0 |
Scleroderma, Localized A term used to describe a variety of localized asymmetrical SKIN thickening that is similar to those of SYSTEMIC SCLERODERMA but without the disease features in the multiple internal organs and BLOOD VESSELS. Lesions may be characterized as patches or plaques (morphea), bands (linear), or nodules. | 0 | 3.67 | 10 | 0 |
Viral Conjunctivitis [description not available] | 0 | 5.21 | 18 | 0 |
Genetic Skin Diseases [description not available] | 0 | 3.57 | 5 | 0 |
Conjunctivitis, Viral Inflammation, often mild, of the conjunctiva caused by a variety of viral agents. Conjunctival involvement may be part of a systemic infection. | 0 | 5.21 | 18 | 0 |
Hemorrhage, Vitreous [description not available] | 0 | 7.8 | 25 | 1 |
Vitreous Hemorrhage Hemorrhage into the VITREOUS BODY. | 0 | 7.8 | 25 | 1 |
Loeys-Dietz Aortic Aneurysm Syndrome Loeys-Dietz Syndrome with aortic aneurysm or dissection. | 0 | 2.6 | 1 | 0 |
Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. | 0 | 3.2 | 5 | 0 |
Lupus Erythematosus, Cutaneous, Subacute [description not available] | 0 | 2.6 | 1 | 0 |
Brown Tendon Sheath Syndrome [description not available] | 0 | 8.57 | 50 | 0 |
Lupus Erythematosus, Cutaneous A form of lupus erythematosus in which the skin may be the only organ involved or in which skin involvement precedes the spread into other body systems. It has been classified into three forms - acute (= LUPUS ERYTHEMATOSUS, SYSTEMIC with skin lesions), subacute, and chronic (= LUPUS ERYTHEMATOSUS, DISCOID). | 0 | 2.6 | 1 | 0 |
Sickle Cell Trait The condition of being heterozygous for hemoglobin S. | 0 | 2.58 | 2 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 6.27 | 20 | 0 |
Eye Foreign Bodies Inanimate objects that become enclosed in the eye. | 0 | 11.19 | 184 | 2 |
Tick Bites The effects, both local and systemic, caused by the bites of TICKS. | 0 | 2.6 | 1 | 0 |
Amaurosis, Leber Congenital [description not available] | 0 | 3.84 | 11 | 0 |
Leber Congenital Amaurosis A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells. | 0 | 3.84 | 11 | 0 |
Breast Cancer [description not available] | 0 | 14.72 | 25 | 3 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 9.72 | 25 | 3 |
Brucella Infection [description not available] | 0 | 5.2 | 20 | 0 |
Brucellosis Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss. | 0 | 5.2 | 20 | 0 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 7.47 | 70 | 0 |
Giant Cell Arteritis A systemic autoimmune disorder that typically affects medium and large ARTERIES, usually leading to occlusive granulomatous vasculitis with transmural infiltrate containing multinucleated GIANT CELLS. The TEMPORAL ARTERY is commonly involved. This disorder appears primarily in people over the age of 50. Symptoms include FEVER; FATIGUE; HEADACHE; visual impairment; pain in the jaw and tongue; and aggravation of pain by cold temperatures. (From Adams et al., Principles of Neurology, 6th ed) | 0 | 7.47 | 70 | 0 |
Myositis, Orbital [description not available] | 0 | 4.39 | 4 | 0 |
Granulomatosis, Wegener's [description not available] | 0 | 6.75 | 27 | 0 |
Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN. | 0 | 11.75 | 27 | 0 |
Xeroderma [description not available] | 0 | 9.86 | 8 | 0 |
Ichthyosis Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome. | 0 | 4.86 | 8 | 0 |
Dandy-Walker Complex [description not available] | 0 | 2.72 | 3 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 2.6 | 1 | 0 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 2.6 | 1 | 0 |
Licheniform Eruptions [description not available] | 0 | 3.51 | 2 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 5.09 | 10 | 0 |
Lichen Ruber Planus [description not available] | 0 | 3.9 | 3 | 0 |
Lichen Planus An inflammatory, pruritic disease of the skin and mucous membranes, which can be either generalized or localized. It is characterized by distinctive purplish, flat-topped papules having a predilection for the trunk and flexor surfaces. The lesions may be discrete or coalesce to form plaques. Histologically, there is a saw-tooth pattern of epidermal hyperplasia and vacuolar alteration of the basal layer of the epidermis along with an intense upper dermal inflammatory infiltrate composed predominantly of T-cells. Etiology is unknown. | 0 | 3.9 | 3 | 0 |
Persistent Fetal Vasculature Syndrome [description not available] | 0 | 2.81 | 3 | 0 |
Asystole [description not available] | 0 | 3.58 | 9 | 0 |
Heart Arrest Cessation of heart beat or MYOCARDIAL CONTRACTION. If it is treated within a few minutes, heart arrest can be reversed in most cases to normal cardiac rhythm and effective circulation. | 0 | 3.58 | 9 | 0 |
Gammapathy, Monoclonal [description not available] | 0 | 4.26 | 7 | 0 |
Paraproteinemias A group of related diseases characterized by an unbalanced or disproportionate proliferation of immunoglobulin-producing cells, usually from a single clone. These cells frequently secrete a structurally homogeneous immunoglobulin (M-component) and/or an abnormal immunoglobulin. | 0 | 4.26 | 7 | 0 |
Posterior Vitreous Detachment [description not available] | 0 | 3.61 | 8 | 0 |
Nevoxanthoendothelioma [description not available] | 0 | 4.47 | 5 | 0 |
Leukemia, Lymphocytic, T Cell [description not available] | 0 | 3.4 | 2 | 0 |
ATLL [description not available] | 0 | 3.97 | 4 | 0 |
Human T-lymphotropic Virus 1 Infection [description not available] | 0 | 5.6 | 9 | 0 |
Leukemia, T-Cell A malignant disease of the T-LYMPHOCYTES in the bone marrow, thymus, and/or blood. | 0 | 3.4 | 2 | 0 |
Leukemia-Lymphoma, Adult T-Cell Aggressive T-Cell malignancy with adult onset, caused by HUMAN T-LYMPHOTROPIC VIRUS 1. It is endemic in Japan, the Caribbean basin, Southeastern United States, Hawaii, and parts of Central and South America and sub-Saharan Africa. | 0 | 3.97 | 4 | 0 |
HTLV-I Infections Diseases caused by HUMAN T-LYMPHOTROPIC VIRUS 1. | 0 | 5.6 | 9 | 0 |
Pyrexia [description not available] | 0 | 5.92 | 25 | 0 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 5.92 | 25 | 0 |
Congenital Ichthyosiform Erythroderma [description not available] | 0 | 2.6 | 1 | 0 |
Pachymeningitis [description not available] | 0 | 4.74 | 32 | 0 |
Meningitis Inflammation of the coverings of the brain and/or spinal cord, which consist of the PIA MATER; ARACHNOID; and DURA MATER. Infections (viral, bacterial, and fungal) are the most common causes of this condition, but subarachnoid hemorrhage (HEMORRHAGES, SUBARACHNOID), chemical irritation (chemical MENINGITIS), granulomatous conditions, neoplastic conditions (CARCINOMATOUS MENINGITIS), and other inflammatory conditions may produce this syndrome. (From Joynt, Clinical Neurology, 1994, Ch24, p6) | 0 | 4.74 | 32 | 0 |
Proliferative Vitreoretinopathy [description not available] | 0 | 6.01 | 18 | 0 |
Vitreoretinopathy, Proliferative Vitreoretinal membrane shrinkage or contraction secondary to the proliferation of primarily retinal pigment epithelial cells and glial cells, particularly fibrous astrocytes, followed by membrane formation. The formation of fibrillar collagen and cellular proliferation appear to be the basis for the contractile properties of the epiretinal and vitreous membranes. | 0 | 6.01 | 18 | 0 |
Arthritis, Spinal [description not available] | 0 | 4.39 | 4 | 0 |
Ocular Hypotension Abnormally low intraocular pressure often related to chronic inflammation (uveitis). | 0 | 8.05 | 30 | 2 |
Debility [description not available] | 0 | 2.6 | 1 | 0 |
HIV Human immunodeficiency virus. A non-taxonomic and historical term referring to any of two species, specifically HIV-1 and/or HIV-2. Prior to 1986, this was called human T-lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). From 1986-1990, it was an official species called HIV. Since 1991, HIV was no longer considered an official species name; the two species were designated HIV-1 and HIV-2. | 0 | 10.09 | 10 | 0 |
Anesthesia A state characterized by loss of feeling or sensation. This depression of nerve function is usually the result of pharmacologic action and is induced to allow performance of surgery or other painful procedures. | 0 | 14.02 | 164 | 5 |
Polychondritis, Chronic Atrophic [description not available] | 0 | 4.14 | 6 | 0 |
Polychondritis, Relapsing An acquired disease of unknown etiology, chronic course, and tendency to recur. It is characterized by inflammation and degeneration of cartilage and can result in deformities such as floppy ear and saddle nose. Loss of cartilage in the respiratory tract can lead to respiratory obstruction. | 0 | 4.14 | 6 | 0 |
Dengue Hemorrhagic Fever [description not available] | 0 | 3.52 | 1 | 0 |
Severe Dengue A virulent form of dengue characterized by THROMBOCYTOPENIA and an increase in vascular permeability (grades I and II) and distinguished by a positive pain test (e.g., TOURNIQUET PAIN TEST). When accompanied by SHOCK (grades III and IV), it is called dengue shock syndrome. | 0 | 3.52 | 1 | 0 |
Solitary Fibrous Tumors Rare neoplasms of mesenchymal origin, usually benign, and most commonly involving the PLEURA (see SOLITARY FIBROUS TUMOR, PLEURAL). They also are found in extrapleural sites. | 0 | 4.21 | 3 | 0 |
Chronic Progressive External Ophthalmoplegia [description not available] | 0 | 4.3 | 7 | 0 |
Adult-Onset Dystonias [description not available] | 0 | 2.69 | 3 | 0 |
Dystonic Disorders Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset. | 0 | 2.69 | 3 | 0 |
Acute Pain Intensely discomforting, distressful, or agonizing sensation associated with trauma or disease, with well-defined location, character, and timing. | 0 | 2.6 | 1 | 0 |
Uveal Neoplasms Tumors or cancer of the UVEA. | 0 | 9.93 | 67 | 2 |
Epiretinal Membrane A membrane on the vitreal surface of the retina resulting from the proliferation of one or more of three retinal elements: (1) fibrous astrocytes; (2) fibrocytes; and (3) RETINAL PIGMENT EPITHELIUM. Localized epiretinal membranes may occur at the posterior pole of the eye without clinical signs or may cause marked loss of vision as a result of covering, distorting, or detaching the FOVEA CENTRALIS. Epiretinal membranes may cause vascular leakage and secondary retinal edema. In younger individuals some membranes appear to be developmental in origin and occur in otherwise normal eyes. The majority occur in association with RETINAL HOLES, ocular concussions, retinal inflammation, or after ocular surgery. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p291) | 0 | 11.49 | 15 | 1 |
Blood Poisoning [description not available] | 0 | 6.7 | 22 | 0 |
Infectious Diseases [description not available] | 0 | 5.13 | 11 | 0 |
Feline Infectious Peritonitis Common coronavirus infection of cats caused by the feline infectious peritonitis virus (CORONAVIRUS, FELINE). The disease is characterized by a long incubation period, fever, depression, loss of appetite, wasting, and progressive abdominal enlargement. Infection of cells of the monocyte-macrophage lineage appears to be essential in FIP pathogenesis. | 0 | 8.01 | 3 | 0 |
Communicable Diseases An illness caused by an infectious agent or its toxins that occurs through the direct or indirect transmission of the infectious agent or its products from an infected individual or via an animal, vector or the inanimate environment to a susceptible animal or human host. | 0 | 5.13 | 11 | 0 |
Sepsis Systemic inflammatory response syndrome with a proven or suspected infectious etiology. When sepsis is associated with organ dysfunction distant from the site of infection, it is called severe sepsis. When sepsis is accompanied by HYPOTENSION despite adequate fluid infusion, it is called SEPTIC SHOCK. | 0 | 11.7 | 22 | 0 |
Exfoliation Glaucoma [description not available] | 0 | 9.15 | 34 | 1 |
Exfoliation Syndrome The deposition of flaky, translucent fibrillar material most conspicuous on the anterior lens capsule and pupillary margin but also in both surfaces of the iris, the zonules, trabecular meshwork, ciliary body, corneal endothelium, and orbital blood vessels. It sometimes forms a membrane on the anterior iris surface. Exfoliation refers to the shedding of pigment by the iris. (Newell, Ophthalmology, 7th ed, p380) | 0 | 14.15 | 34 | 1 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 7.22 | 21 | 2 |
Cerebral Concussion [description not available] | 0 | 3.21 | 6 | 0 |
Dizzyness [description not available] | 0 | 5.41 | 5 | 1 |
Central Nervous System Origin Vertigo [description not available] | 0 | 6.85 | 30 | 0 |
Brain Concussion A nonspecific term used to describe transient alterations or loss of consciousness following closed head injuries. The duration of UNCONSCIOUSNESS generally lasts a few seconds, but may persist for several hours. Concussions may be classified as mild, intermediate, and severe. Prolonged periods of unconsciousness (often defined as greater than 6 hours in duration) may be referred to as post-traumatic coma (COMA, POST-HEAD INJURY). (From Rowland, Merritt's Textbook of Neurology, 9th ed, p418) | 0 | 8.21 | 6 | 0 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 5.41 | 5 | 1 |
Vertigo An illusion of movement, either of the external world revolving around the individual or of the individual revolving in space. Vertigo may be associated with disorders of the inner ear (EAR, INNER); VESTIBULAR NERVE; BRAINSTEM; or CEREBRAL CORTEX. Lesions in the TEMPORAL LOBE and PARIETAL LOBE may be associated with FOCAL SEIZURES that may feature vertigo as an ictal manifestation. (From Adams et al., Principles of Neurology, 6th ed, pp300-1) | 0 | 6.85 | 30 | 0 |
Facial Palsy [description not available] | 0 | 10.4 | 23 | 0 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 4.42 | 8 | 0 |
Recrudescence [description not available] | 0 | 10.38 | 76 | 1 |
Cytomegalic Inclusion Disease [description not available] | 0 | 12.33 | 36 | 0 |
Cytomegalovirus Infections Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults. | 0 | 7.33 | 36 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 3.45 | 2 | 0 |
Cancer of Kidney [description not available] | 0 | 4.51 | 9 | 0 |
Carcinoma, Renal Cell A heterogeneous group of sporadic or hereditary carcinoma derived from cells of the KIDNEYS. There are several subtypes including the clear cells, the papillary, the chromophobe, the collecting duct, the spindle cells (sarcomatoid), or mixed cell-type carcinoma. | 0 | 3.45 | 2 | 0 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 4.51 | 9 | 0 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 12.16 | 15 | 1 |
Meibomian Gland Dysfunction A chronic dysfunction of MEIBOMIAN GLANDS characterized by altered tear film stability and function due to a decrease or alteration in lipid quality/content in meibum. It is often associated with evaporative-type DRY EYE SYNDROME. | 0 | 4.07 | 3 | 0 |
Central Serous Retinopathy [description not available] | 0 | 4.59 | 9 | 0 |
Central Serous Chorioretinopathy A visual impairment characterized by the accumulation of fluid under the retina through a defect in the retinal pigment epithelium. | 0 | 9.59 | 9 | 0 |
Vitiligo A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. | 0 | 7.53 | 12 | 1 |
Kahler Disease [description not available] | 0 | 4.09 | 16 | 0 |
Multiple Myeloma A malignancy of mature PLASMA CELLS engaging in monoclonal immunoglobulin production. It is characterized by hyperglobulinemia, excess Bence-Jones proteins (free monoclonal IMMUNOGLOBULIN LIGHT CHAINS) in the urine, skeletal destruction, bone pain, and fractures. Other features include ANEMIA; HYPERCALCEMIA; and RENAL INSUFFICIENCY. | 0 | 9.09 | 16 | 0 |
Action Tremor [description not available] | 0 | 4.16 | 17 | 0 |
Tremor Cyclical movement of a body part that can represent either a physiologic process or a manifestation of disease. Intention or action tremor, a common manifestation of CEREBELLAR DISEASES, is aggravated by movement. In contrast, resting tremor is maximal when there is no attempt at voluntary movement, and occurs as a relatively frequent manifestation of PARKINSON DISEASE. | 0 | 4.16 | 17 | 0 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 5.87 | 13 | 0 |
Amyotrophic Lateral Sclerosis A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) | 0 | 5.87 | 13 | 0 |
Libman-Sacks Disease [description not available] | 0 | 9.57 | 47 | 1 |
Lupus Erythematosus, Systemic A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys, and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. | 0 | 9.57 | 47 | 1 |
Keratoconjunctivitis Sicca Drying and inflammation of the conjunctiva as a result of insufficient lacrimal secretion. When found in association with XEROSTOMIA and polyarthritis, it is called SJOGREN'S SYNDROME. | 0 | 24.77 | 195 | 2 |
Neuritis A general term indicating inflammation of a peripheral or cranial nerve. Clinical manifestation may include PAIN; PARESTHESIAS; PARESIS; or HYPESTHESIA. | 0 | 10.84 | 99 | 0 |
Diabetes Mellitus, Gestational [description not available] | 0 | 2.6 | 1 | 0 |
Diabetes, Gestational Diabetes mellitus induced by PREGNANCY but resolved at the end of pregnancy. It does not include previously diagnosed diabetics who become pregnant (PREGNANCY IN DIABETICS). Gestational diabetes usually develops in late pregnancy when insulin antagonistic hormones peaks leading to INSULIN RESISTANCE; GLUCOSE INTOLERANCE; and HYPERGLYCEMIA. | 0 | 2.6 | 1 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 10.42 | 54 | 2 |
Arthritis, Rheumatoid A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated. | 0 | 10.42 | 54 | 2 |
Laurence-Moon-Bardet-Biedl Syndrome [description not available] | 0 | 3.1 | 5 | 0 |
Bardet-Biedl Syndrome An autosomal recessive disorder characterized by RETINITIS PIGMENTOSA; POLYDACTYLY; OBESITY; MENTAL RETARDATION; hypogenitalism; renal dysplasia; and short stature. This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME. (From J Med Genet 1997 Feb;34(2):92-8) | 0 | 3.1 | 5 | 0 |
Feminization Development of female secondary SEX CHARACTERISTICS in the MALE. It is due to the effects of estrogenic metabolites of precursors from endogenous or exogenous sources, such as ADRENAL GLANDS or therapeutic drugs. | 0 | 2.72 | 2 | 0 |
Microcephaly A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.) | 0 | 6.74 | 22 | 0 |
Choroid Diseases Disorders of the choroid including hereditary choroidal diseases, neoplasms, and other abnormalities of the vascular layer of the uvea. | 0 | 7.43 | 33 | 0 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 4.39 | 8 | 0 |
Benedict Syndrome [description not available] | 0 | 2.6 | 1 | 0 |
Parasite Infections [description not available] | 0 | 3.67 | 10 | 0 |
Akinetic-Rigid Variant of Huntington Disease [description not available] | 0 | 5.22 | 11 | 1 |
Huntington Disease A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4) | 0 | 5.22 | 11 | 1 |
Bleeding [description not available] | 0 | 11.45 | 132 | 2 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 11.45 | 132 | 2 |
Allergy, Food [description not available] | 0 | 3.24 | 6 | 0 |
Food Hypersensitivity Gastrointestinal disturbances, skin eruptions, or shock due to allergic reactions to allergens in food. | 0 | 3.24 | 6 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 4.7 | 11 | 0 |
Arnold-Chiari Deformity [description not available] | 0 | 3.72 | 3 | 0 |
Astrocytoma Neoplasms of the brain and spinal cord derived from glial cells which vary from histologically benign forms to highly anaplastic and malignant tumors. Fibrillary astrocytomas are the most common type and may be classified in order of increasing malignancy (grades I through IV). In the first two decades of life, astrocytomas tend to originate in the cerebellar hemispheres; in adults, they most frequently arise in the cerebrum and frequently undergo malignant transformation. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2013-7; Holland et al., Cancer Medicine, 3d ed, p1082) | 0 | 9.7 | 11 | 0 |
Atrophy, Muscular, Peroneal [description not available] | 0 | 2.81 | 3 | 0 |
Charcot-Marie-Tooth Disease A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343) | 0 | 2.81 | 3 | 0 |
Optic Atrophy Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition. | 0 | 14.24 | 105 | 1 |
Anti-GBM Disease [description not available] | 0 | 3.1 | 5 | 0 |
Anti-Glomerular Basement Membrane Disease An autoimmune disease of the KIDNEY and the LUNG. It is characterized by the presence of circulating autoantibodies targeting the epitopes in the non-collagenous domains of COLLAGEN TYPE IV in the basement membranes of kidney glomeruli (KIDNEY GLOMERULUS) and lung alveoli (PULMONARY ALVEOLI), and the subsequent destruction of these basement membranes. Clinical features include pulmonary alveolar hemorrhage and glomerulonephritis. | 0 | 3.1 | 5 | 0 |
Sparganosis Infection of animals, including fish and man, with a developmental stage of Diphyllobothrium. This stage has recently been referred to as a plerocercoid but the name sparganum has persisted. Therefore, infection of fish or other animals with the plerocercoid larvae is sparganosis. Fish-eating mammals, including man, are the final hosts. | 0 | 2.93 | 4 | 0 |
Anisocoria Unequal pupil size, which may represent a benign physiologic variant or a manifestation of disease. Pathologic anisocoria reflects an abnormality in the musculature of the iris (IRIS DISEASES) or in the parasympathetic or sympathetic pathways that innervate the pupil. Physiologic anisocoria refers to an asymmetry of pupil diameter, usually less than 2mm, that is not associated with disease. | 0 | 8.25 | 6 | 0 |
Dacryoadenitis [description not available] | 0 | 4.96 | 15 | 0 |
Craniofacial Pain [description not available] | 0 | 5.29 | 7 | 0 |
Facial Pain Pain in the facial region including orofacial pain and craniofacial pain. Associated conditions include local inflammatory and neoplastic disorders and neuralgic syndromes involving the trigeminal, facial, and glossopharyngeal nerves. Conditions which feature recurrent or persistent facial pain as the primary manifestation of disease are referred to as FACIAL PAIN SYNDROMES. | 0 | 10.29 | 7 | 0 |
Aprosodia [description not available] | 0 | 2.89 | 4 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 6.41 | 23 | 2 |
Intraocular Lymphoma A form of malignant cancer which occurs within the eyeball. | 0 | 2.76 | 2 | 0 |
Deep Vein Thrombosis [description not available] | 0 | 6.19 | 31 | 0 |
Cancer of Prostate [description not available] | 0 | 3.13 | 5 | 0 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 3.13 | 5 | 0 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 6.19 | 31 | 0 |
Leucocythaemia [description not available] | 0 | 8.75 | 44 | 1 |
Benign Intracranial Hypertension [description not available] | 0 | 6.78 | 14 | 1 |
Leukemia A progressive, malignant disease of the blood-forming organs, characterized by distorted proliferation and development of leukocytes and their precursors in the blood and bone marrow. Leukemias were originally termed acute or chronic based on life expectancy but now are classified according to cellular maturity. Acute leukemias consist of predominately immature cells; chronic leukemias are composed of more mature cells. (From The Merck Manual, 2006) | 0 | 8.75 | 44 | 1 |
Pseudotumor Cerebri A condition marked by raised intracranial pressure and characterized clinically by HEADACHES; NAUSEA; PAPILLEDEMA, peripheral constriction of the visual fields, transient visual obscurations, and pulsatile TINNITUS. OBESITY is frequently associated with this condition, which primarily affects women between 20 and 44 years of age. Chronic PAPILLEDEMA may lead to optic nerve injury (see OPTIC NERVE DISEASES) and visual loss (see BLINDNESS). | 0 | 6.78 | 14 | 1 |
Acute Peripheral Vestibulopathy [description not available] | 0 | 3.66 | 8 | 0 |
Vestibular Neuronitis Idiopathic inflammation of the VESTIBULAR NERVE, characterized clinically by the acute or subacute onset of VERTIGO; NAUSEA; and imbalance. The COCHLEAR NERVE is typically spared and HEARING LOSS and TINNITUS do not usually occur. Symptoms usually resolve over a period of days to weeks. (Adams et al., Principles of Neurology, 6th ed, p304) | 0 | 3.66 | 8 | 0 |
Cochlear Hearing Loss [description not available] | 0 | 3.82 | 11 | 0 |
Auditory Vertigo [description not available] | 0 | 4.7 | 11 | 0 |
Hearing Loss, Sensorineural Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM. | 0 | 3.82 | 11 | 0 |
Meniere Disease A disease of the inner ear (LABYRINTH) that is characterized by fluctuating SENSORINEURAL HEARING LOSS; TINNITUS; episodic VERTIGO; and aural fullness. It is the most common form of endolymphatic hydrops. | 0 | 4.7 | 11 | 0 |
Drusen, Retinal [description not available] | 0 | 6.04 | 10 | 1 |
Bone Fractures [description not available] | 0 | 5.68 | 14 | 0 |
Fractures, Bone Breaks in bones. | 0 | 5.68 | 14 | 0 |
Cardiac Death [description not available] | 0 | 5.41 | 15 | 0 |
Capillary Leak Syndrome A condition characterized by recurring episodes of fluid leaking from capillaries into extra-vascular compartments causing hematocrit to rise precipitously. If not treated, generalized vascular leak can lead to generalized EDEMA; SHOCK; cardiovascular collapse; and MULTIPLE ORGAN FAILURE. | 0 | 2.6 | 1 | 0 |
Congenital Erythropoietic Porphyria [description not available] | 0 | 2.6 | 1 | 0 |
Break-Bone Fever [description not available] | 0 | 4.56 | 9 | 0 |
Dengue An acute febrile disease transmitted by the bite of AEDES mosquitoes infected with DENGUE VIRUS. It is self-limiting and characterized by fever, myalgia, headache, and rash. SEVERE DENGUE is a more virulent form of dengue. | 0 | 4.56 | 9 | 0 |
Retinal Arterial Macroaneurysm An acquired dilation of the retinal artery often associated with systemic HYPERTENSION. | 0 | 2.6 | 1 | 0 |
Angiitis [description not available] | 0 | 7.87 | 21 | 0 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 12.87 | 21 | 0 |
Systemic Vasculitis A heterogeneous group of diseases characterized by inflammation and necrosis of the blood vessel walls. | 0 | 8.52 | 1 | 0 |
Cicatrization The formation of fibrous tissue in the place of normal tissue during the process of WOUND HEALING. It includes scar tissue formation occurring in healing internal organs as well as in the skin after surface injuries. | 0 | 7.27 | 46 | 0 |
Chorioretinitis Inflammation of the choroid in which the sensory retina becomes edematous and opaque. The inflammatory cells and exudate may burst through the sensory retina to cloud the vitreous body. | 0 | 6.27 | 59 | 0 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 7.27 | 46 | 0 |
Epileptiform Neuralgia [description not available] | 0 | 4.75 | 7 | 1 |
Trigeminal Neuralgia A syndrome characterized by recurrent episodes of excruciating pain lasting several seconds or longer in the sensory distribution of the TRIGEMINAL NERVE. Pain may be initiated by stimulation of trigger points on the face, lips, or gums or by movement of facial muscles or chewing. Associated conditions include MULTIPLE SCLEROSIS, vascular anomalies, ANEURYSMS, and neoplasms. (Adams et al., Principles of Neurology, 6th ed, p187) | 0 | 9.75 | 7 | 1 |
Lymphoma of Mucosa-Associated Lymphoid Tissue [description not available] | 0 | 4.07 | 5 | 0 |
Lymphoma, B-Cell, Marginal Zone Extranodal lymphoma of lymphoid tissue associated with mucosa that is in contact with exogenous antigens. Many of the sites of these lymphomas, such as the stomach, salivary gland, and thyroid, are normally devoid of lymphoid tissue. They acquire mucosa-associated lymphoid tissue (MALT) type as a result of an immunologically mediated disorder. | 0 | 4.07 | 5 | 0 |
CCMMT [description not available] | 0 | 3.52 | 1 | 0 |
Conjunctival Neoplasms Tumors or cancer of the CONJUNCTIVA. | 0 | 5.89 | 17 | 0 |
Heart Disease, Ischemic [description not available] | 0 | 2.6 | 1 | 0 |
Myocardial Ischemia A disorder of cardiac function caused by insufficient blood flow to the muscle tissue of the heart. The decreased blood flow may be due to narrowing of the coronary arteries (CORONARY ARTERY DISEASE), to obstruction by a thrombus (CORONARY THROMBOSIS), or less commonly, to diffuse narrowing of arterioles and other small vessels within the heart. Severe interruption of the blood supply to the myocardial tissue may result in necrosis of cardiac muscle (MYOCARDIAL INFARCTION). | 0 | 2.6 | 1 | 0 |
Low Tension Glaucoma A form of glaucoma in which chronic optic nerve damage and loss of vision normally attributable to buildup of intraocular pressure occurs despite prevailing conditions of normal intraocular pressure. | 0 | 6.03 | 17 | 0 |
Thalassemias [description not available] | 0 | 4.17 | 6 | 0 |
Thalassemia A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia. | 0 | 4.17 | 6 | 0 |
Hematuria Presence of blood in the urine. | 0 | 2.44 | 2 | 0 |
Hematochezia The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea. | 0 | 2.9 | 4 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 2.9 | 4 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 5.21 | 12 | 0 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 10.21 | 12 | 0 |
Cirrhosis, Liver [description not available] | 0 | 5.58 | 11 | 0 |
Alcoholic Cirrhosis [description not available] | 0 | 2.6 | 1 | 0 |
Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. | 0 | 5.58 | 11 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 2.6 | 1 | 0 |
Brain Dead [description not available] | 0 | 4.74 | 7 | 0 |
Gelineau Syndrome [description not available] | 0 | 2.37 | 2 | 0 |
Narcolepsy A condition characterized by recurrent episodes of daytime somnolence and lapses in consciousness (microsomnias) that may be associated with automatic behaviors and AMNESIA. CATAPLEXY; SLEEP PARALYSIS, and hypnagogic HALLUCINATIONS frequently accompany narcolepsy. The pathophysiology of this disorder includes sleep-onset rapid eye movement (REM) sleep, which normally follows stage III or IV sleep. (From Neurology 1998 Feb;50(2 Suppl 1):S2-S7) | 0 | 7.37 | 2 | 0 |
Allergy, Drug [description not available] | 0 | 11.27 | 51 | 3 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 11.27 | 51 | 3 |
Hallucination of Body Sensation [description not available] | 0 | 5.06 | 17 | 0 |
Hallucinations Subjectively experienced sensations in the absence of an appropriate stimulus, but which are regarded by the individual as real. They may be of organic origin or associated with MENTAL DISORDERS. | 0 | 5.06 | 17 | 0 |
Peripheral Nerve Diseases [description not available] | 0 | 7.63 | 16 | 1 |
Encephalomyopathies, Mitochondrial [description not available] | 0 | 3.52 | 1 | 0 |
Peripheral Nervous System Diseases Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves. | 0 | 7.63 | 16 | 1 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 13.86 | 30 | 1 |
Cleft Palate, Isolated [description not available] | 0 | 4.36 | 21 | 0 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 9.36 | 21 | 0 |
Benign Meningeal Neoplasms [description not available] | 0 | 6.08 | 30 | 0 |
Compartment Syndromes Conditions in which increased pressure within a limited space compromises the BLOOD CIRCULATION and function of tissue within that space. Some of the causes of increased pressure are TRAUMA, tight dressings, HEMORRHAGE, and exercise. Sequelae include nerve compression (NERVE COMPRESSION SYNDROMES); PARALYSIS; and ISCHEMIC CONTRACTURE. FASCIOTOMY is often used to decompress increased pressure and eliminate pain associated with compartment syndromes. | 0 | 4.33 | 7 | 0 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 6.08 | 30 | 0 |
Great Pox [description not available] | 0 | 5.26 | 55 | 0 |
Syphilis A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM. | 0 | 5.26 | 55 | 0 |
Phlegmon [description not available] | 0 | 4.82 | 13 | 0 |
Cellulitis An acute, diffuse, and suppurative inflammation of loose connective tissue, particularly the deep subcutaneous tissues, and sometimes muscle, which is most commonly seen as a result of infection of a wound, ulcer, or other skin lesions. | 0 | 4.82 | 13 | 0 |
Psychoses [description not available] | 0 | 5.48 | 16 | 1 |
Psychotic Disorders Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994) | 0 | 5.48 | 16 | 1 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 7.86 | 62 | 0 |
Complication, Intraoperative [description not available] | 0 | 8.33 | 27 | 3 |
Ankylosing Spondylarthritis [description not available] | 0 | 4.75 | 12 | 0 |
Spondylitis, Ankylosing A chronic inflammatory condition affecting the axial joints, such as the SACROILIAC JOINT and other intervertebral or costovertebral joints. It occurs predominantly in young males and is characterized by pain and stiffness of joints (ANKYLOSIS) with inflammation at tendon insertions. | 0 | 4.75 | 12 | 0 |
Idiopathic Hypoparathyroidism A condition of low or absent PTH level and HYPOCALCEMIA. It usually occurs as part of an autoimmune syndrome. | 0 | 3.32 | 7 | 0 |
Spasmophilia [description not available] | 0 | 2.86 | 4 | 0 |
Hypocalcemia Reduction of the blood calcium below normal. Manifestations include hyperactive deep tendon reflexes, Chvostek's sign, muscle and abdominal cramps, and carpopedal spasm. (Dorland, 27th ed) | 0 | 2.42 | 2 | 0 |
Hypoparathyroidism A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone. | 0 | 3.32 | 7 | 0 |
Aphthae [description not available] | 0 | 3.09 | 4 | 0 |
Stomatitis, Aphthous A recurrent disease of the oral mucosa of unknown etiology. It is characterized by small white ulcerative lesions, single or multiple, round or oval. Two to eight crops of lesions occur per year, lasting for 7 to 14 days and then heal without scarring. (From Jablonski's Dictionary of Dentistry, 1992, p742) | 0 | 3.09 | 4 | 0 |
Bruise [description not available] | 0 | 6.77 | 24 | 1 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 6.77 | 24 | 1 |
Hemorrhage, Retinal [description not available] | 0 | 8.02 | 84 | 0 |
Disbacteriosis [description not available] | 0 | 3.64 | 2 | 0 |
Fisher Syndrome [description not available] | 0 | 7.79 | 3 | 0 |
ADDH [description not available] | 0 | 8.38 | 18 | 1 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 3.21 | 5 | 0 |
Age-Related Memory Disorders [description not available] | 0 | 5.21 | 6 | 0 |
Attention Deficit Disorder with Hyperactivity A behavior disorder originating in childhood in which the essential features are signs of developmentally inappropriate inattention, impulsivity, and hyperactivity. Although most individuals have symptoms of both inattention and hyperactivity-impulsivity, one or the other pattern may be predominant. The disorder is more frequent in males than females. Onset is in childhood. Symptoms often attenuate during late adolescence although a minority experience the full complement of symptoms into mid-adulthood. (From DSM-V) | 0 | 8.38 | 18 | 1 |
Depressive Disorder, Major Disorder in which five (or more) of the following symptoms have been present during the same 2-week period and represent a change from previous functioning; at least one of the symptoms is either (1) depressed mood or (2) loss of interest or pleasure. Symptoms include: depressed mood most of the day, nearly every daily; markedly diminished interest or pleasure in activities most of the day, nearly every day; significant weight loss when not dieting or weight gain; Insomnia or hypersomnia nearly every day; psychomotor agitation or retardation nearly every day; fatigue or loss of energy nearly every day; feelings of worthlessness or excessive or inappropriate guilt; diminished ability to think or concentrate, or indecisiveness, nearly every day; or recurrent thoughts of death, recurrent suicidal ideation without a specific plan, or a suicide attempt. (DSM-5) | 0 | 3.21 | 5 | 0 |
Memory Disorders Disturbances in registering an impression, in the retention of an acquired impression, or in the recall of an impression. Memory impairments are associated with DEMENTIA; CRANIOCEREBRAL TRAUMA; ENCEPHALITIS; ALCOHOLISM (see also ALCOHOL AMNESTIC DISORDER); SCHIZOPHRENIA; and other conditions. | 0 | 5.21 | 6 | 0 |
Acropachy, Hereditary [description not available] | 0 | 2.6 | 1 | 0 |
Autotomy Human [description not available] | 0 | 3.75 | 11 | 0 |
Vestibular Diseases Pathological processes of the VESTIBULAR LABYRINTH which contains part of the balancing apparatus. Patients with vestibular diseases show instability and are at risk of frequent falls. | 0 | 5.95 | 9 | 1 |
Autosomal Dominant Cerebellar Ataxia, Type II [description not available] | 0 | 3.01 | 4 | 0 |
Spinocerebellar Ataxias A group of predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43) | 0 | 3.01 | 4 | 0 |
Drug Overdose Accidental or deliberate use of a medication or street drug in excess of normal dosage. | 0 | 2.6 | 1 | 0 |
Capillary Telangiectasia, Brain [description not available] | 0 | 5.33 | 20 | 0 |
Deafness, Transitory [description not available] | 0 | 4.1 | 16 | 0 |
Deaf Mutism [description not available] | 0 | 6.26 | 36 | 0 |
Scotoma A localized defect in the visual field bordered by an area of normal vision. This occurs with a variety of EYE DISEASES (e.g., RETINAL DISEASES and GLAUCOMA); OPTIC NERVE DISEASES, and other conditions. | 0 | 5.04 | 43 | 0 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 6.26 | 36 | 0 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 4.1 | 16 | 0 |
Diseases of Immune System [description not available] | 0 | 6.53 | 35 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 6.53 | 35 | 0 |
Retinal Degeneration A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304) | 0 | 10.06 | 148 | 0 |
Epithelial Ovarian Cancer [description not available] | 0 | 3.52 | 1 | 0 |
Carcinoma, Ovarian Epithelial A malignant neoplasm that originates in cells on the surface EPITHELIUM of the ovary and is the most common form of ovarian cancer. There are five histologic subtypes: papillary serous, endometrioid, mucinous, clear cell, and transitional cell. Mutations in BRCA1, OPCML, PRKN, PIK3CA, AKT1, CTNNB1, RRAS2, and CDH1 genes are associated with this cancer. | 0 | 3.52 | 1 | 0 |
Bacterial Meningitides [description not available] | 0 | 2.48 | 2 | 0 |
Meningitis, Bacterial Bacterial infections of the leptomeninges and subarachnoid space, frequently involving the cerebral cortex, cranial nerves, cerebral blood vessels, spinal cord, and nerve roots. | 0 | 2.48 | 2 | 0 |
Nervous System Disorders [description not available] | 0 | 8.71 | 64 | 0 |
Nervous System Diseases Diseases of the central and peripheral nervous system. This includes disorders of the brain, spinal cord, cranial nerves, peripheral nerves, nerve roots, autonomic nervous system, neuromuscular junction, and muscle. | 0 | 8.71 | 64 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial [description not available] | 0 | 2.6 | 1 | 0 |
Lymphohistiocytosis, Hemophagocytic A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 2.6 | 1 | 0 |
Cushing's Syndrome [description not available] | 0 | 3.56 | 3 | 0 |
Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. | 0 | 3.56 | 3 | 0 |
Neuroendocrine Tumors Tumors whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumors include ectopic hormone production (often via APUD CELLS), the presence of tumor-associated antigens, and isozyme composition. | 0 | 8.64 | 2 | 0 |
Dermatitis, Contact, Phototoxic [description not available] | 0 | 8.23 | 29 | 0 |
Congenital Myotonic Dystrophy [description not available] | 0 | 4.95 | 15 | 0 |
Myotonic Dystrophy Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2. | 0 | 9.95 | 15 | 0 |
Craniocerebral Injuries [description not available] | 0 | 6.62 | 38 | 0 |
Craniocerebral Trauma Traumatic injuries involving the cranium and intracranial structures (i.e., BRAIN; CRANIAL NERVES; MENINGES; and other structures). Injuries may be classified by whether or not the skull is penetrated (i.e., penetrating vs. nonpenetrating) or whether there is an associated hemorrhage. | 0 | 6.62 | 38 | 0 |
Acute Retinal Necrosis [description not available] | 0 | 8.8 | 11 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 7.09 | 29 | 0 |
Neurodegenerative Diseases Hereditary and sporadic conditions which are characterized by progressive nervous system dysfunction. These disorders are often associated with atrophy of the affected central or peripheral nervous system structures. | 0 | 12.09 | 29 | 0 |
Measles, German [description not available] | 0 | 6.28 | 21 | 0 |
Urogenital Prolapse [description not available] | 0 | 2.6 | 1 | 0 |
Pelvic Organ Prolapse Abnormal descent of a pelvic organ resulting in the protrusion of the organ beyond its normal anatomical confines. Symptoms often include vaginal discomfort, DYSPAREUNIA; URINARY STRESS INCONTINENCE; and FECAL INCONTINENCE. | 0 | 2.6 | 1 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 8.92 | 57 | 0 |
Polycystic Ovarian Syndrome [description not available] | 0 | 4.25 | 3 | 0 |
Polycystic Ovary Syndrome A complex disorder characterized by infertility, HIRSUTISM; OBESITY; and various menstrual disturbances such as OLIGOMENORRHEA; AMENORRHEA; ANOVULATION. Polycystic ovary syndrome is usually associated with bilateral enlarged ovaries studded with atretic follicles, not with cysts. The term, polycystic ovary, is misleading. | 0 | 4.25 | 3 | 0 |
Elephant Man Disease [description not available] | 0 | 3.52 | 1 | 0 |
Proteus Syndrome Hamartoneoplastic malformation syndrome of uncertain etiology characterized by partial GIGANTISM of the hands and/or feet, asymmetry of the limbs, plantar hyperplasia, hemangiomas (HEMANGIOMA), lipomas (LIPOMA), lymphangiomas (LYMPHANGIOMA), epidermal NEVI; MACROCEPHALY; cranial HYPEROSTOSIS, and long-bone overgrowth. Joseph Merrick, the so-called elephant man, apparently suffered from Proteus syndrome and not NEUROFIBROMATOSIS, a disorder with similar characteristics. | 0 | 3.52 | 1 | 0 |
Child Development Deviations [description not available] | 0 | 5.03 | 15 | 0 |
Developmental Disabilities Disorders in which there is a delay in development based on that expected for a given age level or stage of development. These impairments or disabilities originate before age 18, may be expected to continue indefinitely, and constitute a substantial impairment. Biological and nonbiological factors are involved in these disorders. (From American Psychiatric Glossary, 6th ed) | 0 | 5.03 | 15 | 0 |
Pain, Chronic [description not available] | 0 | 4.4 | 2 | 0 |
Chronic Pain Aching sensation that persists for more than a few months. It may or may not be associated with trauma or disease, and may persist after the initial injury has healed. Its localization, character, and timing are more vague than with acute pain. | 0 | 4.4 | 2 | 0 |
Weight Reduction [description not available] | 0 | 4.08 | 5 | 0 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 4.08 | 5 | 0 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 7.53 | 52 | 0 |
Wounds and Injuries Damage inflicted on the body as the direct or indirect result of an external force, with or without disruption of structural continuity. | 0 | 7.53 | 52 | 0 |
Diathesis [description not available] | 0 | 8.26 | 41 | 0 |
Genome Instability [description not available] | 0 | 2.77 | 3 | 0 |
Constricted Pupil [description not available] | 0 | 4.68 | 28 | 0 |
Miosis Pupillary constriction. This may result from congenital absence of the dilatator pupillary muscle, defective sympathetic innervation, or irritation of the CONJUNCTIVA or CORNEA. | 0 | 4.68 | 28 | 0 |
Enophthalmos Recession of the eyeball into the orbit. | 0 | 7.83 | 16 | 1 |
Arthritis, Juvenile Chronic [description not available] | 0 | 5.78 | 22 | 0 |
Arthritis, Juvenile Arthritis in children, with onset before 16 years of age. The terms juvenile rheumatoid arthritis (JRA) and juvenile idiopathic arthritis (JIA) refer to classification systems for chronic arthritis in children. Only one subtype of juvenile arthritis (polyarticular-onset, rheumatoid factor-positive) clinically resembles adult rheumatoid arthritis and is considered its childhood equivalent. | 0 | 5.78 | 22 | 0 |
Familial Exudative Vitreoretinopathies A group of inherited disorders characterized by incomplete development of the retinal vasculature. Its severity can vary from complete blindness in infancy, to mild or no visual problems, where small areas of vascular defects are observable only by FLUORESCEIN ANGIOGRAPHY. Exudative vitreoretinopathy 1 is associated with mutations in the FZD4 gene. | 0 | 2.78 | 3 | 0 |
Central Nervous System Toxoplasmosis [description not available] | 0 | 3.02 | 4 | 0 |
Toxoplasmosis, Animal Acquired infection of non-human animals by organisms of the genus TOXOPLASMA. | 0 | 4.38 | 21 | 0 |
Toxoplasmosis, Cerebral Infections of the BRAIN caused by the protozoan TOXOPLASMA gondii that primarily arise in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES (see also AIDS-RELATED OPPORTUNISTIC INFECTIONS). The infection may involve the brain diffusely or form discrete abscesses. Clinical manifestations include SEIZURES, altered mentation, headache, focal neurologic deficits, and INTRACRANIAL HYPERTENSION. (From Joynt, Clinical Neurology, 1998, Ch27, pp41-3) | 0 | 3.02 | 4 | 0 |
Digestive System Disorders [description not available] | 0 | 5.96 | 5 | 0 |
Disease, Pulmonary [description not available] | 0 | 7.39 | 17 | 0 |
ACD-MPV [description not available] | 0 | 3.12 | 1 | 0 |
Blood Clot [description not available] | 0 | 8.08 | 79 | 0 |
Emesis [description not available] | 0 | 8.18 | 25 | 2 |
Colicky Pain [description not available] | 0 | 3.39 | 2 | 0 |
Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | 0 | 5.96 | 5 | 0 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 7.39 | 17 | 0 |
Persistent Fetal Circulation Syndrome A syndrome of persistent PULMONARY HYPERTENSION in the newborn infant (INFANT, NEWBORN) without demonstrable HEART DISEASES. This neonatal condition can be caused by severe pulmonary vasoconstriction (reactive type), hypertrophy of pulmonary arterial muscle (hypertrophic type), or abnormally developed pulmonary arterioles (hypoplastic type). The newborn patient exhibits CYANOSIS and ACIDOSIS due to the persistence of fetal circulatory pattern of right-to-left shunting of blood through a patent ductus arteriosus (DUCTUS ARTERIOSUS, PATENT) and at times a patent foramen ovale (FORAMEN OVALE, PATENT). | 0 | 3.12 | 1 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 8.08 | 79 | 0 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 13.18 | 25 | 2 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 3.39 | 2 | 0 |
Corneal Wavefront Aberration Asymmetries in the topography and refractive index of the corneal surface that affect visual acuity. | 0 | 6.03 | 9 | 1 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 5.77 | 20 | 0 |
Reperfusion Injury Adverse functional, metabolic, or structural changes in tissues that result from the restoration of blood flow to the tissue (REPERFUSION) following ISCHEMIA. | 0 | 5.77 | 20 | 0 |
Candida Infection [description not available] | 0 | 6.66 | 21 | 1 |
Candidiasis Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ed) | 0 | 6.66 | 21 | 1 |
Prolapse The protrusion of an organ or part of an organ into a natural or artificial orifice. | 0 | 8.23 | 6 | 0 |
Cadaver A dead body, usually a human body. | 0 | 7.15 | 61 | 0 |
Eye Infections, Fungal Infection by a variety of fungi, usually through four possible mechanisms: superficial infection producing conjunctivitis, keratitis, or lacrimal obstruction; extension of infection from neighboring structures - skin, paranasal sinuses, nasopharynx; direct introduction during surgery or accidental penetrating trauma; or via the blood or lymphatic routes in patients with underlying mycoses. | 0 | 8.7 | 34 | 1 |
Child Mental Disorders [description not available] | 0 | 2.63 | 2 | 0 |
Abnormality, Heart [description not available] | 0 | 5.35 | 23 | 0 |
Heart Defects, Congenital Developmental abnormalities involving structures of the heart. These defects are present at birth but may be discovered later in life. | 0 | 5.35 | 23 | 0 |
Neurodevelopmental Disorders These are a group of conditions with onset in the developmental period. The disorders typically manifest early in development, often before the child enters grade school, and are characterized by developmental deficits that produce impairments of personal, social, academic, or occupational functioning. (From DSM-5). | 0 | 2.63 | 2 | 0 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 6.11 | 31 | 0 |
Cerebral Hemorrhage Bleeding into one or both CEREBRAL HEMISPHERES including the BASAL GANGLIA and the CEREBRAL CORTEX. It is often associated with HYPERTENSION and CRANIOCEREBRAL TRAUMA. | 0 | 11.11 | 31 | 0 |
Occupational Injuries Injuries sustained from incidents in the course of work-related activities. | 0 | 4.02 | 4 | 0 |
Arrhythmia [description not available] | 0 | 11.66 | 21 | 0 |
Arrhythmias, Cardiac Any disturbances of the normal rhythmic beating of the heart or MYOCARDIAL CONTRACTION. Cardiac arrhythmias can be classified by the abnormalities in HEART RATE, disorders of electrical impulse generation, or impulse conduction. | 0 | 6.66 | 21 | 0 |
Benign Paroxysmal Positional Vertigo Idiopathic recurrent VERTIGO associated with POSITIONAL NYSTAGMUS. It is associated with a vestibular loss without other neurological or auditory signs. Unlike in LABYRINTHITIS and VESTIBULAR NEURONITIS, inflammation in the ear is not observed. | 0 | 3.79 | 3 | 0 |
Adenocarcinoma, Sebaceous A malignant tumor composed of cells showing differentiation toward sebaceous epithelium. The tumor is solitary, firm, somewhat raised, more or less translucent, and covered with normal or slightly verrucose epidermis. It may be yellow or orange. The face and scalp are the commonest sites. The growth can be slow or rapid but metastasis is uncommon. Surgery cures most of the cases. (From Rook et al., Textbook of Dermatology, 4th ed, pp2403-4) | 0 | 3.39 | 2 | 0 |
Neoplasms, Sebaceous Gland [description not available] | 0 | 4.31 | 4 | 0 |
Carbohydrate-Deficient Glycoprotein Syndrome [description not available] | 0 | 4.66 | 5 | 0 |
Congenital Disorders of Glycosylation A genetically heterogeneous group of heritable disorders resulting from defects in protein N-glycosylation. | 0 | 4.66 | 5 | 0 |
Cutis Elastica [description not available] | 0 | 3.2 | 6 | 0 |
Ehlers-Danlos Syndrome A heterogeneous group of autosomally inherited COLLAGEN DISEASES caused by defects in the synthesis or structure of FIBRILLAR COLLAGEN. There are numerous subtypes: classical, hypermobility, vascular, and others. Common clinical features include hyperextensible skin and joints, skin fragility and reduced wound healing capability. | 0 | 3.2 | 6 | 0 |
Infections, Helicobacter [description not available] | 0 | 3.41 | 2 | 0 |
Helicobacter Infections Infections with organisms of the genus HELICOBACTER, particularly, in humans, HELICOBACTER PYLORI. The clinical manifestations are focused in the stomach, usually the gastric mucosa and antrum, and the upper duodenum. This infection plays a major role in the pathogenesis of type B gastritis and peptic ulcer disease. | 0 | 3.41 | 2 | 0 |
Arthritis, Post-Infectious [description not available] | 0 | 4.37 | 8 | 0 |
Arthritis, Reactive An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN. | 0 | 4.37 | 8 | 0 |
Benign Optic Nerve Neoplasm [description not available] | 0 | 3.88 | 12 | 0 |
Infections, Vibrio [description not available] | 0 | 3 | 4 | 0 |
Abdominal Migraine [description not available] | 0 | 6.94 | 41 | 0 |
Dorsolateral Medullary Syndrome [description not available] | 0 | 2.94 | 4 | 0 |
Migraine Disorders A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 6.94 | 41 | 0 |
Angle's Classification [description not available] | 0 | 4.37 | 7 | 0 |
Malocclusion Such malposition and contact of the maxillary and mandibular teeth as to interfere with the highest efficiency during the excursive movements of the jaw that are essential for mastication. (Jablonski, Illustrated Dictionary of Dentistry, 1982) | 0 | 9.37 | 7 | 0 |
Bone Loss, Osteoclastic [description not available] | 0 | 3.8 | 4 | 0 |
Aberrant Tissue [description not available] | 0 | 5.21 | 19 | 0 |
Abnormalities, Congenital, Nervous System [description not available] | 0 | 5.04 | 9 | 0 |
Catarrh Inflammation of a mucous membrane with increased flow of mucous in humans or animals. Catarrh is used mostly in a historical context. | 0 | 4.02 | 2 | 1 |
Common Cold A catarrhal disorder of the upper respiratory tract, which may be viral or a mixed infection. It generally involves a runny nose, nasal congestion, and sneezing. | 0 | 4.02 | 2 | 1 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 6.04 | 29 | 0 |
Pre-Eclampsia A complication of PREGNANCY, characterized by a complex of symptoms including maternal HYPERTENSION and PROTEINURIA with or without pathological EDEMA. Symptoms may range between mild and severe. Pre-eclampsia usually occurs after the 20th week of gestation, but may develop before this time in the presence of trophoblastic disease. | 0 | 11.04 | 29 | 0 |
Arterial Obstructive Diseases [description not available] | 0 | 8.19 | 77 | 0 |
Arterial Occlusive Diseases Pathological processes which result in the partial or complete obstruction of ARTERIES. They are characterized by greatly reduced or absence of blood flow through these vessels. They are also known as arterial insufficiency. | 0 | 13.19 | 77 | 0 |
Asymptomatic Conditions [description not available] | 0 | 3.74 | 3 | 0 |
Keratitis, Acanthamoeba [description not available] | 0 | 3.31 | 6 | 0 |
Acanthamoeba Keratitis Infection of the cornea by an ameboid protozoan which may cause corneal ulceration leading to blindness. | 0 | 3.31 | 6 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 6.66 | 12 | 1 |
Albinism General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair. | 0 | 7.01 | 56 | 0 |
Inner Ear Disease [description not available] | 0 | 9.29 | 7 | 0 |
Labyrinth Diseases Pathological processes of the inner ear (LABYRINTH) which contains the essential apparatus of hearing (COCHLEA) and balance (SEMICIRCULAR CANALS). | 0 | 4.29 | 7 | 0 |
Endolymphatic Hydrops An accumulation of ENDOLYMPH in the inner ear (LABYRINTH) leading to buildup of pressure and distortion of intralabyrinthine structures, such as COCHLEA and SEMICIRCULAR CANALS. It is characterized by SENSORINEURAL HEARING LOSS; TINNITUS; and sometimes VERTIGO. | 0 | 3.45 | 2 | 0 |
Eye Diseases, Hereditary Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder. | 0 | 7.01 | 29 | 0 |
Deafness-Retinitis Pigmentosa Syndrome [description not available] | 0 | 3.05 | 4 | 0 |
Cognitive Decline [description not available] | 0 | 3.28 | 5 | 0 |
Academic Disorder, Developmental [description not available] | 0 | 3.29 | 6 | 0 |
Learning Disabilities Conditions characterized by a significant discrepancy between an individual's perceived level of intellect and their ability to acquire new language and other cognitive skills. These may result from organic or psychological conditions. Relatively common subtypes include DYSLEXIA, DYSCALCULIA, and DYSGRAPHIA. | 0 | 3.29 | 6 | 0 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 3.28 | 5 | 0 |
Adipocere [description not available] | 0 | 6.71 | 31 | 0 |
Chemical Dependence [description not available] | 0 | 7.7 | 17 | 1 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 7.7 | 17 | 1 |
Drusen, Optic Disc [description not available] | 0 | 4.35 | 7 | 0 |
Poisoning Used with drugs, chemicals, and industrial materials for human or animal poisoning, acute or chronic, whether the poisoning is accidental, occupational, suicidal, by medication error, or by environmental exposure. | 0 | 6.14 | 32 | 0 |
Amyloidosis A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. | 0 | 9.23 | 18 | 0 |
Anal Cancer [description not available] | 0 | 3.12 | 1 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 8.41 | 44 | 1 |
Female Genital Neoplasms [description not available] | 0 | 3.12 | 1 | 0 |
Male Genital Neoplasms [description not available] | 0 | 3.12 | 1 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 5.9 | 17 | 0 |
Anus Neoplasms Tumors or cancer of the ANAL CANAL. | 0 | 3.12 | 1 | 0 |
Carcinoma, Squamous Cell A carcinoma derived from stratified SQUAMOUS EPITHELIAL CELLS. It may also occur in sites where glandular or columnar epithelium is normally present. (From Stedman, 25th ed) | 0 | 8.41 | 44 | 1 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 3.12 | 1 | 0 |
Genital Neoplasms, Male Tumor or cancer of the MALE GENITALIA. | 0 | 3.12 | 1 | 0 |
Ciliopathies Genetic disorders caused by defects in genes related to the primary CILIUM; BASAL BODY; or CENTROSOME. Primary features may include obesity, SKELETAL DYSPLASIA; POLYDACTYLY and malformations that primarily involve the liver, eye or kidneys. | 0 | 2.55 | 2 | 0 |
Anoxemia [description not available] | 0 | 7.13 | 49 | 0 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 7.13 | 49 | 0 |
Neoplasms, Squamous Cell Neoplasms of the SQUAMOUS EPITHELIAL CELLS. The concept does not refer to neoplasms located in tissue composed of squamous elements. | 0 | 2.82 | 2 | 0 |
Behavior Disorders [description not available] | 0 | 7.18 | 43 | 0 |
Absence Seizure [description not available] | 0 | 9.43 | 40 | 1 |
Mental Disorders Psychiatric illness or diseases manifested by breakdowns in the adaptational process expressed primarily as abnormalities of thought, feeling, and behavior producing either distress or impairment of function. | 0 | 7.18 | 43 | 0 |
Seizures Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder. | 0 | 9.43 | 40 | 1 |
Facial Spasm, Unilateral [description not available] | 0 | 2.91 | 3 | 0 |
Arbovirus Infections Infections caused by arthropod-borne viruses, general or unspecified. | 0 | 4.26 | 4 | 0 |
Familial Spastic Paraparesis, Htlv-1-Associated [description not available] | 0 | 2.48 | 2 | 0 |
Paraparesis, Tropical Spastic A subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the Caribbean, Colombia, India, and Africa, as well as in the southwestern region of Japan; associated with infection by HUMAN T-CELL LEUKEMIA VIRUS I. Clinical manifestations include a slowly progressive spastic weakness of the legs, increased reflexes, Babinski signs, incontinence, and loss of vibratory and position sensation. On pathologic examination inflammatory, demyelination, and necrotic lesions may be found in the spinal cord. (Adams et al., Principles of Neurology, 6th ed, p1239) | 0 | 2.48 | 2 | 0 |
Embolus [description not available] | 0 | 6.4 | 30 | 0 |
Embolism Blocking of a blood vessel by an embolus which can be a blood clot or other undissolved material in the blood stream. | 0 | 6.4 | 30 | 0 |
Fasciolopsiasis [description not available] | 0 | 4.96 | 38 | 0 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 5.83 | 23 | 0 |
CACH Syndrome [description not available] | 0 | 3.17 | 1 | 0 |
Familial Precocious Puberty [description not available] | 0 | 3.31 | 2 | 0 |
Puberty, Precocious Development of SEXUAL MATURATION in boys and girls at a chronological age that is 2.5 standard deviations below the mean age at onset of PUBERTY in the population. This early maturation of the hypothalamic-pituitary-gonadal axis results in sexual precocity, elevated serum levels of GONADOTROPINS and GONADAL STEROID HORMONES such as ESTRADIOL and TESTOSTERONE. | 0 | 3.31 | 2 | 0 |
Acute Autoimmune Neuropathy [description not available] | 0 | 4.55 | 10 | 0 |
Guillain-Barre Syndrome An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (From Adams et al., Principles of Neurology, 6th ed, pp1312-1314) | 0 | 4.55 | 10 | 0 |
Plant Poisoning Poisoning by the ingestion of plants or its leaves, berries, roots or stalks. The manifestations in both humans and animals vary in severity from mild to life threatening. In animals, especially domestic animals, it is usually the result of ingesting moldy or fermented forage. | 0 | 3.22 | 6 | 0 |
Dermatitis Any inflammation of the skin. | 0 | 5.06 | 17 | 0 |
Acariasis [description not available] | 0 | 2.9 | 3 | 0 |
47,XX,+21 [description not available] | 0 | 4.4 | 22 | 0 |
Aura [description not available] | 0 | 9.45 | 40 | 1 |
Down Syndrome A chromosome disorder associated either with an extra chromosome 21 or an effective trisomy for chromosome 21. Clinical manifestations include hypotonia, short stature, brachycephaly, upslanting palpebral fissures, epicanthus, Brushfield spots on the iris, protruding tongue, small ears, short, broad hands, fifth finger clinodactyly, Simian crease, and moderate to severe INTELLECTUAL DISABILITY. Cardiac and gastrointestinal malformations, a marked increase in the incidence of LEUKEMIA, and the early onset of ALZHEIMER DISEASE are also associated with this condition. Pathologic features include the development of NEUROFIBRILLARY TANGLES in neurons and the deposition of AMYLOID BETA-PROTEIN, similar to the pathology of ALZHEIMER DISEASE. (Menkes, Textbook of Child Neurology, 5th ed, p213) | 0 | 9.4 | 22 | 0 |
Epilepsy A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313) | 0 | 9.45 | 40 | 1 |
Sclerosis, Systemic [description not available] | 0 | 6.34 | 15 | 1 |
Scleroderma, Systemic A chronic multi-system disorder of CONNECTIVE TISSUE. It is characterized by SCLEROSIS in the SKIN, the LUNGS, the HEART, the GASTROINTESTINAL TRACT, the KIDNEYS, and the MUSCULOSKELETAL SYSTEM. Other important features include diseased small BLOOD VESSELS and AUTOANTIBODIES. The disorder is named for its most prominent feature (hard skin), and classified into subsets by the extent of skin thickening: LIMITED SCLERODERMA and DIFFUSE SCLERODERMA. | 0 | 6.34 | 15 | 1 |
Aniseikonia A condition in which the ocular image of an object as seen by one eye differs in size and shape from that seen by the other. | 0 | 9.46 | 24 | 0 |
Genital Tract Infections [description not available] | 0 | 2.25 | 1 | 0 |
Infections, Chlamydia [description not available] | 0 | 6.27 | 25 | 0 |
Chlamydia Infections Infections with bacteria of the genus CHLAMYDIA. | 0 | 6.27 | 25 | 0 |
Infections, Coronavirus [description not available] | 0 | 8.43 | 18 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 8.22 | 16 | 0 |
Coronavirus Infections Virus diseases caused by the CORONAVIRUS genus. Some specifics include transmissible enteritis of turkeys (ENTERITIS, TRANSMISSIBLE, OF TURKEYS); FELINE INFECTIOUS PERITONITIS; and transmissible gastroenteritis of swine (GASTROENTERITIS, TRANSMISSIBLE, OF SWINE). | 0 | 8.43 | 18 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 4.05 | 3 | 0 |
Orbital Neoplasms Neoplasms of the bony orbit and contents except the eyeball. | 0 | 9.16 | 106 | 0 |
Lymphangioma A benign tumor resulting from a congenital malformation of the lymphatic system. Lymphangioendothelioma is a type of lymphangioma in which endothelial cells are the dominant component. | 0 | 4.05 | 3 | 0 |
Acute Post-operative Pain [description not available] | 0 | 7.3 | 15 | 8 |
Pain, Postoperative Pain during the period after surgery. | 0 | 7.3 | 15 | 8 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 6.6 | 29 | 0 |
Alexia [description not available] | 0 | 6.14 | 20 | 0 |
Shaken Baby Syndrome Brain injuries resulted from vigorous shaking of an infant or young child held by the chest, shoulders, or extremities causing extreme cranial acceleration. It is characterized by the intracranial and intraocular hemorrhages with no evident external trauma. Serious cases may result in death. | 0 | 9.12 | 5 | 0 |
Central Hypothyroidism [description not available] | 0 | 5.8 | 22 | 0 |
Hypothyroidism A syndrome that results from abnormally low secretion of THYROID HORMONES from the THYROID GLAND, leading to a decrease in BASAL METABOLIC RATE. In its most severe form, there is accumulation of MUCOPOLYSACCHARIDES in the SKIN and EDEMA, known as MYXEDEMA. It may be primary or secondary due to other pituitary disease, or hypothalamic dysfunction. | 0 | 5.8 | 22 | 0 |
Chromosomal Duplication [description not available] | 0 | 2.25 | 1 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 11.2 | 169 | 2 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 6.96 | 42 | 0 |
Carotid Artery Diseases Pathological conditions involving the CAROTID ARTERIES, including the common, internal, and external carotid arteries. ATHEROSCLEROSIS and TRAUMA are relatively frequent causes of carotid artery pathology. | 0 | 11.2 | 169 | 2 |
Intracranial Aneurysm Abnormal outpouching in the wall of intracranial blood vessels. Most common are the saccular (berry) aneurysms located at branch points in CIRCLE OF WILLIS at the base of the brain. Vessel rupture results in SUBARACHNOID HEMORRHAGE or INTRACRANIAL HEMORRHAGES. Giant aneurysms ( | 0 | 11.96 | 42 | 0 |
Leukemic Infiltration A pathologic change in leukemia in which leukemic cells permeate various organs at any stage of the disease. All types of leukemia show various degrees of infiltration, depending upon the type of leukemia. The degree of infiltration may vary from site to site. The liver and spleen are common sites of infiltration, the greatest appearing in myelocytic leukemia, but infiltration is seen also in the granulocytic and lymphocytic types. The kidney is also a common site and of the gastrointestinal system, the stomach and ileum are commonly involved. In lymphocytic leukemia the skin is often infiltrated. The central nervous system too is a common site. | 0 | 7.12 | 23 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 4.7 | 11 | 0 |
Leukemia, Myeloid, Acute Clonal expansion of myeloid blasts in bone marrow, blood, and other tissue. Myeloid leukemias develop from changes in cells that normally produce NEUTROPHILS; BASOPHILS; EOSINOPHILS; and MONOCYTES. | 0 | 4.7 | 11 | 0 |
Amyloid Neuropathy Type 1 [description not available] | 0 | 4.6 | 9 | 0 |
Amyloid Neuropathies, Familial Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN. | 0 | 4.6 | 9 | 0 |
Avian Diseases [description not available] | 0 | 6.77 | 33 | 0 |
Acute Edematous Pancreatitis [description not available] | 0 | 4.27 | 4 | 0 |
Pancreatitis INFLAMMATION of the PANCREAS. Pancreatitis is classified as acute unless there are computed tomographic or endoscopic retrograde cholangiopancreatographic findings of CHRONIC PANCREATITIS (International Symposium on Acute Pancreatitis, Atlanta, 1992). The two most common forms of acute pancreatitis are ALCOHOLIC PANCREATITIS and gallstone pancreatitis. | 0 | 4.27 | 4 | 0 |
Cancer of Paranasal Sinus [description not available] | 0 | 6.38 | 29 | 0 |
Paranasal Sinus Neoplasms Tumors or cancer of the PARANASAL SINUSES. | 0 | 6.38 | 29 | 0 |
Rheumatism [description not available] | 0 | 7.42 | 34 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 7.42 | 34 | 0 |
Hamartoma A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area. | 0 | 2.91 | 4 | 0 |
Fundus Flavimaculatus [description not available] | 0 | 2.66 | 2 | 0 |
Stargardt Disease A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases. | 0 | 7.66 | 2 | 0 |
Trypanosomiasis Infection with protozoa of the genus TRYPANOSOMA. | 0 | 3.55 | 9 | 0 |
Kawasaki Disease [description not available] | 0 | 3.27 | 6 | 0 |
Mucocutaneous Lymph Node Syndrome An acute, febrile, mucocutaneous condition accompanied by swelling of cervical lymph nodes in infants and young children. The principal symptoms are fever, congestion of the ocular conjunctivae, reddening of the lips and oral cavity, protuberance of tongue papillae, and edema or erythema of the extremities. | 0 | 3.27 | 6 | 0 |
Neoplasms, Skull Base [description not available] | 0 | 5.19 | 7 | 0 |
Poultry Diseases Diseases of birds which are raised as a source of meat or eggs for human consumption and are usually found in barnyards, hatcheries, etc. The concept is differentiated from BIRD DISEASES which is for diseases of birds not considered poultry and usually found in zoos, parks, and the wild. | 0 | 5.79 | 36 | 0 |
Anemia, Hypoplastic [description not available] | 0 | 4.28 | 7 | 0 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 5.4 | 10 | 0 |
Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | 0 | 4.28 | 7 | 0 |
Yellow Fever An acute infectious disease primarily of the tropics, caused by a virus and transmitted to man by mosquitoes of the genera Aedes and Haemagogus. The severe form is characterized by fever, HEMOLYTIC JAUNDICE, and renal damage. | 0 | 7.5 | 2 | 0 |
Blennorrhea, Inclusion [description not available] | 0 | 3.83 | 12 | 0 |
Conjunctivitis, Inclusion An infection of the eyes characterized by the presence in conjunctival epithelial cells of inclusion bodies indistinguishable from those of trachoma. It is acquired by infants during birth and by adults from swimming pools. The etiological agent is CHLAMYDIA TRACHOMATIS whose natural habitat appears to be the genito-urinary tract. Inclusion conjunctivitis is a less severe disease than trachoma and usually clears up spontaneously. | 0 | 3.83 | 12 | 0 |
Chronic Kidney Failure [description not available] | 0 | 5.09 | 17 | 0 |
Kidney Failure, Chronic The end-stage of CHRONIC RENAL INSUFFICIENCY. It is characterized by the severe irreversible kidney damage (as measured by the level of PROTEINURIA) and the reduction in GLOMERULAR FILTRATION RATE to less than 15 ml per min (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002). These patients generally require HEMODIALYSIS or KIDNEY TRANSPLANTATION. | 0 | 5.09 | 17 | 0 |
Asymptomatic Colonization [description not available] | 0 | 2.69 | 2 | 0 |
Infectious Keratoconjunctivitis [description not available] | 0 | 10.24 | 19 | 0 |
Bovine Diseases [description not available] | 0 | 5.71 | 84 | 0 |
Moraxella Infections [description not available] | 0 | 3.05 | 4 | 0 |
Hyphema Bleeding in the anterior chamber of the eye. | 0 | 6.37 | 29 | 0 |
Zoonoses Diseases of non-human animals that may be transmitted to HUMANS or may be transmitted from humans to non-human animals. | 0 | 3.71 | 10 | 0 |
Alloxan Diabetes [description not available] | 0 | 7.09 | 82 | 0 |
Epiphora [description not available] | 0 | 8.28 | 23 | 1 |
Lacrimal Apparatus Diseases Diseases of the LACRIMAL APPARATUS. | 0 | 8.28 | 23 | 1 |
Organophosphorus Poisoning [description not available] | 0 | 3.82 | 2 | 0 |
Organophosphate Poisoning Poisoning due to exposure to ORGANOPHOSPHORUS COMPOUNDS, such as ORGANOPHOSPHATES; ORGANOTHIOPHOSPHATES; and ORGANOTHIOPHOSPHONATES. | 0 | 3.82 | 2 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 4.04 | 3 | 0 |
Cerebral Microangiopathies [description not available] | 0 | 3.17 | 1 | 0 |
Cerebral Small Vessel Diseases Pathological processes or diseases where cerebral MICROVESSELS show abnormalities. They are often associated with aging, hypertension and risk factors for lacunar infarcts (see LACUNAR INFARCTION); LEUKOARAIOSIS; and CEREBRAL HEMORRHAGE. | 0 | 3.17 | 1 | 0 |
Sinusitis, Maxillary [description not available] | 0 | 2.25 | 1 | 0 |
Maxillary Sinusitis Inflammation of the NASAL MUCOSA in the MAXILLARY SINUS. In many cases, it is caused by an infection of the bacteria HAEMOPHILUS INFLUENZAE; STREPTOCOCCUS PNEUMONIAE; or STAPHYLOCOCCUS AUREUS. | 0 | 7.25 | 1 | 0 |
Cerebral Pseudosclerosis [description not available] | 0 | 5.02 | 16 | 0 |
Hepatolenticular Degeneration A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years. | 0 | 5.02 | 16 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 6.99 | 18 | 1 |
Ectopic Ossification [description not available] | 0 | 3.83 | 12 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 15.52 | 258 | 1 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 4.89 | 4 | 0 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 4.38 | 4 | 0 |
Cancer of Lung [description not available] | 0 | 5.94 | 18 | 0 |
Carcinoma, Non-Small-Cell Lung A heterogeneous aggregate of at least three distinct histological types of lung cancer, including SQUAMOUS CELL CARCINOMA; ADENOCARCINOMA; and LARGE CELL CARCINOMA. They are dealt with collectively because of their shared treatment strategy. | 0 | 4.38 | 4 | 0 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 5.94 | 18 | 0 |
Aujeszky Disease [description not available] | 0 | 3.5 | 8 | 0 |
Alcohol Related Neurodevelopmental Disorder [description not available] | 0 | 4.96 | 14 | 0 |
Acne [description not available] | 0 | 7.26 | 9 | 3 |
Acne Vulgaris A chronic disorder of the pilosebaceous apparatus associated with an increase in sebum secretion. It is characterized by open comedones (blackheads), closed comedones (whiteheads), and pustular nodules. The cause is unknown, but heredity and age are predisposing factors. | 0 | 7.26 | 9 | 3 |
Brain Hemorrhage [description not available] | 0 | 5.54 | 6 | 1 |
Arteriovenous Malformations, Cerebral [description not available] | 0 | 3.87 | 12 | 0 |
Deficiency, Mental [description not available] | 0 | 8.92 | 75 | 1 |
Intracranial Arteriovenous Malformations Congenital vascular anomalies in the brain characterized by direct communication between an artery and a vein without passing through the CAPILLARIES. The locations and size of the shunts determine the symptoms including HEADACHES; SEIZURES; STROKE; INTRACRANIAL HEMORRHAGES; mass effect; and vascular steal effect. | 0 | 3.87 | 12 | 0 |
Intellectual Disability Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28) | 0 | 8.92 | 75 | 1 |
Intracranial Hemorrhages Bleeding within the SKULL, including hemorrhages in the brain and the three membranes of MENINGES. The escape of blood often leads to the formation of HEMATOMA in the cranial epidural, subdural, and subarachnoid spaces. | 0 | 10.54 | 6 | 1 |
Angiogranuloma [description not available] | 0 | 2.46 | 2 | 0 |
Dermatomyositis, Adult Type [description not available] | 0 | 4.49 | 9 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 8.8 | 24 | 2 |
Dermatomyositis A subacute or chronic inflammatory disease of muscle and skin, marked by proximal muscle weakness and a characteristic skin rash. The illness occurs with approximately equal frequency in children and adults. The skin lesions usually take the form of a purplish rash (or less often an exfoliative dermatitis) involving the nose, cheeks, forehead, upper trunk, and arms. The disease is associated with a complement mediated intramuscular microangiopathy, leading to loss of capillaries, muscle ischemia, muscle-fiber necrosis, and perifascicular atrophy. The childhood form of this disease tends to evolve into a systemic vasculitis. Dermatomyositis may occur in association with malignant neoplasms. (From Adams et al., Principles of Neurology, 6th ed, pp1405-6) | 0 | 4.49 | 9 | 0 |
Foreign-Body Reaction Chronic inflammation and granuloma formation around irritating foreign bodies. | 0 | 6.84 | 25 | 1 |
Alobar Holoprosencephaly [description not available] | 0 | 5.36 | 14 | 0 |
Chromosome Inversion An aberration in which a chromosomal segment is deleted and reinserted in the same place but turned 180 degrees from its original orientation, so that the gene sequence for the segment is reversed with respect to that of the rest of the chromosome. | 0 | 2.54 | 2 | 0 |
Nevus Flammeus [description not available] | 0 | 2.74 | 3 | 0 |
Port-Wine Stain A vascular malformation of developmental origin characterized pathologically by ectasia of superficial dermal capillaries, and clinically by persistent macular erythema. In the past, port wine stains have frequently been termed capillary hemangiomas, which they are not; unfortunately this confusing practice persists: HEMANGIOMA, CAPILLARY is neoplastic, a port-wine stain is non-neoplastic. Port-wine stains vary in color from fairly pale pink to deep red or purple and in size from a few millimeters to many centimeters in diameter. The face is the most frequently affected site and they are most often unilateral. (From Rook et al., Textbook of Dermatology, 5th ed, p483) | 0 | 7.74 | 3 | 0 |
Buckley Syndrome [description not available] | 0 | 3.17 | 1 | 0 |
Job Syndrome Primary immunodeficiency syndrome characterized by recurrent infections and hyperimmunoglobulinemia E. Most cases are sporadic. Of the rare familial forms, the dominantly inherited subtype has additional connective tissue, dental and skeletal involvement that the recessive type does not share. | 0 | 3.17 | 1 | 0 |
Encephalitis, Japanese B [description not available] | 0 | 2.25 | 1 | 0 |
Encephalitis, Japanese A mosquito-borne encephalitis caused by the Japanese B encephalitis virus (ENCEPHALITIS VIRUS, JAPANESE) occurring throughout Eastern Asia and Australia. The majority of infections occur in children and are subclinical or have features limited to transient fever and gastrointestinal symptoms. Inflammation of the brain, spinal cord, and meninges may occur and lead to transient or permanent neurologic deficits (including a POLIOMYELITIS-like presentation); SEIZURES; COMA; and death. (From Adams et al., Principles of Neurology, 6th ed, p751; Lancet 1998 Apr 11;351(9109):1094-7) | 0 | 2.25 | 1 | 0 |
Fungal Diseases [description not available] | 0 | 7.59 | 48 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 12.59 | 48 | 0 |
Hutchinson Gilford Progeria Syndrome [description not available] | 0 | 4.37 | 8 | 0 |
Progeria An abnormal congenital condition, associated with defects in the LAMIN TYPE A gene, which is characterized by premature aging in children, where all the changes of cell senescence occur. It is manifested by premature graying; hair loss; hearing loss (DEAFNESS); cataracts (CATARACT); ARTHRITIS; OSTEOPOROSIS; DIABETES MELLITUS; atrophy of subcutaneous fat; skeletal hypoplasia; elevated urinary HYALURONIC ACID; and accelerated ATHEROSCLEROSIS. Many affected individuals develop malignant tumors, especially SARCOMA. | 0 | 4.37 | 8 | 0 |
Arthritides, Bacterial [description not available] | 0 | 2.39 | 2 | 0 |
Cardiac Failure [description not available] | 0 | 4.01 | 5 | 0 |
Group A Strep Infection [description not available] | 0 | 5.01 | 15 | 0 |
Bacterial Endocarditides [description not available] | 0 | 3.5 | 8 | 0 |
Endocarditis, Bacterial Inflammation of the ENDOCARDIUM caused by BACTERIA that entered the bloodstream. The strains of bacteria vary with predisposing factors, such as CONGENITAL HEART DEFECTS; HEART VALVE DISEASES; HEART VALVE PROSTHESIS IMPLANTATION; or intravenous drug use. | 0 | 3.5 | 8 | 0 |
Heart Failure A heterogeneous condition in which the heart is unable to pump out sufficient blood to meet the metabolic need of the body. Heart failure can be caused by structural defects, functional abnormalities (VENTRICULAR DYSFUNCTION), or a sudden overload beyond its capacity. Chronic heart failure is more common than acute heart failure which results from sudden insult to cardiac function, such as MYOCARDIAL INFARCTION. | 0 | 4.01 | 5 | 0 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 5.01 | 15 | 0 |
Adult Spinal Muscular Atrophy [description not available] | 0 | 2.25 | 1 | 0 |
Muscular Atrophy, Spinal A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 2.25 | 1 | 0 |
Ganglion Cysts Nodular tumor-like lesions or mucoid flesh, arising from tendon sheaths, LIGAMENTS, or JOINT CAPSULE, especially of the hands, wrists, or feet. They are not true cysts as they lack epithelial wall. They are distinguished from SYNOVIAL CYSTS by the lack of communication with a joint cavity or the SYNOVIAL MEMBRANE. | 0 | 2.37 | 2 | 0 |
Social Anxiety Disorder [description not available] | 0 | 7.9 | 3 | 0 |
Phobia, Social Anxiety disorder characterized by the persistent and irrational fear, anxiety, or avoidance of social or performance situations. | 0 | 2.9 | 3 | 0 |
Muscle Spasm [description not available] | 0 | 8.7 | 34 | 2 |
Spasm An involuntary contraction of a muscle or group of muscles. Spasms may involve SKELETAL MUSCLE or SMOOTH MUSCLE. | 0 | 8.7 | 34 | 2 |
Malignant Hypertension [description not available] | 0 | 9.49 | 9 | 0 |
Hypertension, Malignant A condition of markedly elevated BLOOD PRESSURE with DIASTOLIC PRESSURE usually greater than 120 mm Hg. Malignant hypertension is characterized by widespread vascular damage, PAPILLEDEMA, retinopathy, HYPERTENSIVE ENCEPHALOPATHY, and renal dysfunction. | 0 | 4.49 | 9 | 0 |
Brain Disorders [description not available] | 0 | 7.49 | 72 | 0 |
Infections, RNA Virus [description not available] | 0 | 4.84 | 7 | 1 |
Brain Diseases Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM. | 0 | 7.49 | 72 | 0 |
Vascular Injuries [description not available] | 0 | 3.96 | 5 | 0 |
Cerebrospinal Fluid Drainage [description not available] | 0 | 3.23 | 1 | 0 |
Angioblastic Meningioma [description not available] | 0 | 6.52 | 34 | 0 |
Meningioma A relatively common neoplasm of the CENTRAL NERVOUS SYSTEM that arises from arachnoidal cells. The majority are well differentiated vascular tumors which grow slowly and have a low potential to be invasive, although malignant subtypes occur. Meningiomas have a predilection to arise from the parasagittal region, cerebral convexity, sphenoidal ridge, olfactory groove, and SPINAL CANAL. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2056-7) | 0 | 6.52 | 34 | 0 |
Hemorrhage, Retrobulbar [description not available] | 0 | 4.96 | 8 | 1 |
Histiocytosis, Non-Langerhans-Cell Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group includes HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SINUS HISTIOCYTOSIS; xanthogranuloma; reticulohistiocytoma; JUVENILE XANTHOGRANULOMA; xanthoma disseminatum; as well as the lipid storage diseases (SEA-BLUE HISTIOCYTE SYNDROME; and NIEMANN-PICK DISEASES). | 0 | 2.31 | 1 | 0 |
Disease Resistance The capacity of an organism to defend itself against pathological processes or the agents of those processes. This most often involves innate immunity whereby the organism responds to pathogens in a generic way. The term disease resistance is used most frequently when referring to plants. | 0 | 2.54 | 2 | 0 |
Envenomation, Snakebite [description not available] | 0 | 3.8 | 4 | 0 |
Aqueductal Stenosis [description not available] | 0 | 4.56 | 26 | 0 |
B Virus Infection [description not available] | 0 | 6.75 | 42 | 0 |
Absent Iris [description not available] | 0 | 6.19 | 18 | 0 |
Aniridia A congenital abnormality in which there is only a rudimentary iris. This is due to the failure of the optic cup to grow. Aniridia also occurs in a hereditary form, usually autosomal dominant. | 0 | 6.19 | 18 | 0 |
Emphysema A pathological accumulation of air in tissues or organs. | 0 | 8.6 | 3 | 0 |
Colitis Gravis [description not available] | 0 | 3.25 | 6 | 0 |
Colitis, Ulcerative Inflammation of the COLON that is predominantly confined to the MUCOSA. Its major symptoms include DIARRHEA, rectal BLEEDING, the passage of MUCUS, and ABDOMINAL PAIN. | 0 | 3.25 | 6 | 0 |
Hyperplasia An increase in the number of cells in a tissue or organ without tumor formation. It differs from HYPERTROPHY, which is an increase in bulk without an increase in the number of cells. | 0 | 6.16 | 32 | 0 |
Low Bone Density [description not available] | 0 | 2.47 | 2 | 0 |
Calcification, Pathologic [description not available] | 0 | 7.52 | 37 | 0 |
Bone Diseases, Metabolic Diseases that affect the METABOLIC PROCESSES of BONE TISSUE. | 0 | 2.47 | 2 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 7.52 | 37 | 0 |
Allergy, Latex [description not available] | 0 | 2.25 | 1 | 0 |
Hypermelanosis [description not available] | 0 | 8.35 | 13 | 4 |
Hyperpigmentation Excessive pigmentation of the skin, usually as a result of increased epidermal or dermal melanin pigmentation, hypermelanosis. Hyperpigmentation can be localized or generalized. The condition may arise from exposure to light, chemicals or other substances, or from a primary metabolic imbalance. | 0 | 8.35 | 13 | 4 |
Hyperhomocysteinemia Condition in which the plasma levels of homocysteine and related metabolites are elevated ( | 0 | 4.83 | 7 | 0 |
Neuroma A tumor made up of nerve cells and nerve fibers. (Dorland, 27th ed) | 0 | 4.26 | 7 | 0 |
Situs Inversus A congenital abnormality in which organs in the THORAX and the ABDOMEN are opposite to their normal positions (situs solitus) due to lateral transposition. Normally the STOMACH and SPLEEN are on the left, LIVER on the right, the three-lobed right lung is on the right, and the two-lobed left lung on the left. Situs inversus has a familial pattern and has been associated with a number of genes related to microtubule-associated proteins. | 0 | 2.4 | 2 | 0 |
Postherpetic Neuralgia [description not available] | 0 | 3.17 | 1 | 0 |
Neuralgia, Postherpetic Pain in nerves, frequently involving facial SKIN, resulting from the activation the latent varicella-zoster virus (HERPESVIRUS 3, HUMAN). The two forms of the condition preceding the pain are HERPES ZOSTER OTICUS; and HERPES ZOSTER OPHTHALMICUS. Following the healing of the rashes and blisters, the pain sometimes persists. | 0 | 3.17 | 1 | 0 |
Eye Burns Injury to any part of the eye by extreme heat, chemical agents, or ultraviolet radiation. | 0 | 8.19 | 69 | 0 |
Genetic Diseases, X-Chromosome Linked [description not available] | 0 | 3.77 | 11 | 0 |
Cryptogenic Infantile Spasms [description not available] | 0 | 3.03 | 4 | 0 |
Spasms, Infantile An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8) | 0 | 3.03 | 4 | 0 |
Choroid Neoplasms Tumors of the choroid; most common intraocular tumors are malignant melanomas of the choroid. These usually occur after puberty and increase in incidence with advancing age. Most malignant melanomas of the uveal tract develop from benign melanomas (nevi). | 0 | 7.95 | 79 | 1 |
Autosomal Dominant Hereditary Spastic Paraplegia [description not available] | 0 | 2.55 | 2 | 0 |
Groenblad-Strandberg Syndrome [description not available] | 0 | 6.42 | 16 | 0 |
Pseudoxanthoma Elasticum An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE. | 0 | 6.42 | 16 | 0 |
Spastic Paraplegia, Hereditary A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progressive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8) | 0 | 2.55 | 2 | 0 |
Sneezing The sudden, forceful, involuntary expulsion of air from the NOSE and MOUTH caused by irritation to the MUCOUS MEMBRANES of the upper RESPIRATORY TRACT. | 0 | 5.89 | 3 | 1 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 4.68 | 11 | 0 |
Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. | 0 | 4.68 | 11 | 0 |
Health Care Associated Infection [description not available] | 0 | 3.78 | 11 | 0 |
Human Adenovirus Infections [description not available] | 0 | 3.1 | 5 | 0 |
Adenovirus Infections, Human Respiratory and conjunctival infections caused by 33 identified serotypes of human adenoviruses. | 0 | 3.1 | 5 | 0 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 3.78 | 11 | 0 |
AIDS, Murine [description not available] | 0 | 3.16 | 5 | 0 |
Anti-Phospholipid Antibody Syndrome [description not available] | 0 | 2.75 | 3 | 0 |
Livedo Reticularis A condition characterized by a reticular or fishnet pattern on the skin of lower extremities and other parts of the body. This red and blue pattern is due to deoxygenated blood in unstable dermal blood vessels. The condition is intensified by cold exposure and relieved by rewarming. | 0 | 2.41 | 1 | 0 |
Antiphospholipid Syndrome The presence of antibodies directed against phospholipids (ANTIBODIES, ANTIPHOSPHOLIPID). The condition is associated with a variety of diseases, notably systemic lupus erythematosus and other connective tissue diseases, thrombopenia, and arterial or venous thromboses. In pregnancy it can cause abortion. Of the phospholipids, the cardiolipins show markedly elevated levels of anticardiolipin antibodies (ANTIBODIES, ANTICARDIOLIPIN). Present also are high levels of lupus anticoagulant (LUPUS COAGULATION INHIBITOR). | 0 | 7.75 | 3 | 0 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 4.54 | 9 | 0 |
Acute Idiopathic Facial Neuropathy [description not available] | 0 | 4.22 | 3 | 1 |
Bell Palsy A syndrome characterized by the acute onset of unilateral FACIAL PARALYSIS which progresses over a 2-5 day period. Weakness of the orbicularis oculi muscle and resulting incomplete eye closure may be associated with corneal injury. Pain behind the ear often precedes the onset of paralysis. This condition may be associated with HERPESVIRUS 1, HUMAN infection of the facial nerve. (Adams et al., Principles of Neurology, 6th ed, p1376) | 0 | 9.22 | 3 | 1 |
Central Nervous System Cysticercosis [description not available] | 0 | 2.92 | 4 | 0 |
Parasitic Skin Diseases [description not available] | 0 | 5.54 | 6 | 1 |
Neurocysticercosis Infection of the brain, spinal cord, or perimeningeal structures with the larval forms of the genus TAENIA (primarily T. solium in humans). Lesions formed by the organism are referred to as cysticerci. The infection may be subacute or chronic, and the severity of symptoms depends on the severity of the host immune response and the location and number of lesions. SEIZURES represent the most common clinical manifestation although focal neurologic deficits may occur. (From Joynt, Clinical Neurology, 1998, Ch27, pp46-50) | 0 | 2.92 | 4 | 0 |
Dementia Praecox [description not available] | 0 | 9.17 | 37 | 4 |
Schizophrenia A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior. | 0 | 9.17 | 37 | 4 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 7.1 | 55 | 0 |
Mycoplasma dispar Infection [description not available] | 0 | 2.31 | 1 | 0 |
Acute Brain Injuries [description not available] | 0 | 7.58 | 34 | 1 |
Brain Injuries Acute and chronic (see also BRAIN INJURIES, CHRONIC) injuries to the brain, including the cerebral hemispheres, CEREBELLUM, and BRAIN STEM. Clinical manifestations depend on the nature of injury. Diffuse trauma to the brain is frequently associated with DIFFUSE AXONAL INJURY or COMA, POST-TRAUMATIC. Localized injuries may be associated with NEUROBEHAVIORAL MANIFESTATIONS; HEMIPARESIS, or other focal neurologic deficits. | 0 | 7.58 | 34 | 1 |
Infection, Toxoplasma gondii [description not available] | 0 | 7.47 | 91 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 7.47 | 91 | 0 |
Congenital Syphilis [description not available] | 0 | 9.47 | 9 | 0 |
Syphilis, Congenital Syphilis acquired in utero and manifested by any of several characteristic tooth (Hutchinson's teeth) or bone malformations and by active mucocutaneous syphilis at birth or shortly thereafter. Ocular and neurologic changes may also occur. | 0 | 4.47 | 9 | 0 |
Facies The appearance of the face that is often characteristic of a disease or pathological condition, as the elfin facies of WILLIAMS SYNDROME or the mongoloid facies of DOWN SYNDROME. (Random House Unabridged Dictionary, 2d ed) | 0 | 5.42 | 14 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 8.19 | 119 | 0 |
Atrophy, Muscle [description not available] | 0 | 2.89 | 4 | 0 |
Muscular Atrophy Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation. | 0 | 2.89 | 4 | 0 |
Hakim Syndrome [description not available] | 0 | 3.88 | 4 | 0 |
Hydrocephalus, Normal Pressure A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see GAIT DISORDERS, NEUROLOGIC), progressive intellectual decline, and URINARY INCONTINENCE. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of CSF including SUBARACHNOID HEMORRHAGE, chronic MENINGITIS, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3) | 0 | 3.88 | 4 | 0 |
Insect Bites [description not available] | 0 | 2.71 | 3 | 0 |
Insect Bites and Stings Bites and stings inflicted by insects. | 0 | 2.71 | 3 | 0 |
Acidosis, Diabetic [description not available] | 0 | 3.63 | 3 | 0 |
Diabetic Ketoacidosis A life-threatening complication of diabetes mellitus, primarily of TYPE 1 DIABETES MELLITUS with severe INSULIN deficiency and extreme HYPERGLYCEMIA. It is characterized by KETOSIS; DEHYDRATION; and depressed consciousness leading to COMA. | 0 | 3.63 | 3 | 0 |
Brain Inflammation [description not available] | 0 | 4.74 | 32 | 0 |
Chronic Lymphocytic Thyroiditis [description not available] | 0 | 2.82 | 3 | 0 |
Encephalitis Inflammation of the BRAIN due to infection, autoimmune processes, toxins, and other conditions. Viral infections (see ENCEPHALITIS, VIRAL) are a relatively frequent cause of this condition. | 0 | 9.74 | 32 | 0 |
Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | 0 | 2.82 | 3 | 0 |
Kidney Failure A severe irreversible decline in the ability of kidneys to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. | 0 | 2.6 | 1 | 0 |
Renal Insufficiency Conditions in which the KIDNEYS perform below the normal level in the ability to remove wastes, concentrate URINE, and maintain ELECTROLYTE BALANCE; BLOOD PRESSURE; and CALCIUM metabolism. Renal insufficiency can be classified by the degree of kidney damage (as measured by the level of PROTEINURIA) and reduction in GLOMERULAR FILTRATION RATE. | 0 | 2.6 | 1 | 0 |
Deficiency, Vitamin A [description not available] | 0 | 7.27 | 47 | 0 |
Vitamin A Deficiency A nutritional condition produced by a deficiency of VITAMIN A in the diet, characterized by NIGHT BLINDNESS and other ocular manifestations such as dryness of the conjunctiva and later of the cornea (XEROPHTHALMIA). Vitamin A deficiency is a very common problem worldwide, particularly in developing countries as a consequence of famine or shortages of vitamin A-rich foods. In the United States it is found among the urban poor, the elderly, alcoholics, and patients with malabsorption. (From Cecil Textbook of Medicine, 19th ed, p1179) | 0 | 7.27 | 47 | 0 |
Lung Adenocarcinoma [description not available] | 0 | 2.31 | 1 | 0 |
Adenocarcinoma of Lung A carcinoma originating in the lung and the most common lung cancer type in never-smokers. Malignant cells exhibit distinct features such as glandular epithelial, or tubular morphology. Mutations in KRAS, EGFR, BRAF, and ERBB2 genes are associated with this cancer. | 0 | 2.31 | 1 | 0 |
Brain Swelling [description not available] | 0 | 4.5 | 5 | 0 |
Brain Edema Increased intracellular or extracellular fluid in brain tissue. Cytotoxic brain edema (swelling due to increased intracellular fluid) is indicative of a disturbance in cell metabolism, and is commonly associated with hypoxic or ischemic injuries (see HYPOXIA, BRAIN). An increase in extracellular fluid may be caused by increased brain capillary permeability (vasogenic edema), an osmotic gradient, local blockages in interstitial fluid pathways, or by obstruction of CSF flow (e.g., obstructive HYDROCEPHALUS). (From Childs Nerv Syst 1992 Sep; 8(6):301-6) | 0 | 4.5 | 5 | 0 |
Latent Infection Delayed infection of the host by a dormant or inactive pathogen. | 0 | 2.31 | 1 | 0 |
Synostosis A union between adjacent bones or parts of a single bone formed by osseous material, such as ossified connecting cartilage or fibrous tissue. (Dorland, 27th ed) | 0 | 2.38 | 2 | 0 |
Polyploid [description not available] | 0 | 3.57 | 9 | 0 |
B16 Melanoma [description not available] | 0 | 5.21 | 7 | 0 |
Anemia, Cooley's [description not available] | 0 | 2.37 | 2 | 0 |
beta-Thalassemia A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. | 0 | 2.37 | 2 | 0 |
Intestinal Volvulus A twisting in the intestine (INTESTINES) that can cause INTESTINAL OBSTRUCTION. | 0 | 2.31 | 1 | 0 |
Abnormalities, Digestive System [description not available] | 0 | 2.39 | 2 | 0 |
Alcaptonuria [description not available] | 0 | 3.34 | 7 | 0 |
Ochronosis The yellowish discoloration of connective tissue due to deposition of HOMOGENTISIC ACID (a brown-black pigment). This is due to defects in the metabolism of PHENYLALANINE and TYROSINE. Ochronosis occurs in ALKAPTONURIA, but has also been associated with exposure to certain chemicals (e.g., PHENOL, trinitrophenol, BENZENE DERIVATIVES). | 0 | 8.21 | 6 | 0 |
Alkaptonuria An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS. | 0 | 8.34 | 7 | 0 |
Infarct [description not available] | 0 | 5.55 | 17 | 0 |
Hand Foot and Mouth Disease [description not available] | 0 | 2.31 | 1 | 0 |
Hand, Foot and Mouth Disease A mild, highly infectious viral disease of children, characterized by vesicular lesions in the mouth and on the hands and feet. It is caused by coxsackieviruses A. | 0 | 2.31 | 1 | 0 |
Abdominal Cramps [description not available] | 0 | 3.89 | 2 | 1 |
Abnormal Movements [description not available] | 0 | 2.64 | 3 | 0 |
Low Back Ache [description not available] | 0 | 3.23 | 1 | 0 |
Low Back Pain Acute or chronic pain in the lumbar or sacral regions, which may be associated with musculo-ligamentous SPRAINS AND STRAINS; INTERVERTEBRAL DISK DISPLACEMENT; and other conditions. | 0 | 3.23 | 1 | 0 |
Harelip [description not available] | 0 | 3.91 | 13 | 0 |
Cleft Lip Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region. | 0 | 3.91 | 13 | 0 |
Deficiency, Thiamine [description not available] | 0 | 2.79 | 3 | 0 |
Beriberi, Cerebral [description not available] | 0 | 3.04 | 5 | 0 |
Korsakoff Psychosis [description not available] | 0 | 2.31 | 1 | 0 |
Thiamine Deficiency A nutritional condition produced by a deficiency of THIAMINE in the diet, characterized by anorexia, irritability, and weight loss. Later, patients experience weakness, peripheral neuropathy, headache, and tachycardia. In addition to being caused by a poor diet, thiamine deficiency in the United States most commonly occurs as a result of alcoholism, since ethanol interferes with thiamine absorption. In countries relying on polished rice as a dietary staple, BERIBERI prevalence is very high. (From Cecil Textbook of Medicine, 19th ed, p1171) | 0 | 7.79 | 3 | 0 |
Elevated Cholesterol [description not available] | 0 | 4.15 | 17 | 0 |
Hypercholesterolemia A condition with abnormally high levels of CHOLESTEROL in the blood. It is defined as a cholesterol value exceeding the 95th percentile for the population. | 0 | 4.15 | 17 | 0 |
Onchocerciasis, Ocular Filarial infection of the eyes transmitted from person to person by bites of Onchocerca volvulus-infected black flies. The microfilariae of Onchocerca are thus deposited beneath the skin. They migrate through various tissues including the eye. Those persons infected have impaired vision and up to 20% are blind. The incidence of eye lesions has been reported to be as high as 30% in Central America and parts of Africa. | 0 | 14.09 | 38 | 12 |
Infections, Rickettsia [description not available] | 0 | 3.04 | 5 | 0 |
Inadequate Sleep [description not available] | 0 | 2.93 | 4 | 0 |
Infections, Staphylococcal [description not available] | 0 | 9.27 | 72 | 1 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 9.27 | 72 | 1 |
Polyarthritis [description not available] | 0 | 6.83 | 47 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 6.83 | 47 | 0 |
Anemia, Megaloblastic A disorder characterized by the presence of ANEMIA, abnormally large red blood cells (megalocytes or macrocytes), and MEGALOBLASTS. | 0 | 2.25 | 1 | 0 |
Craniofacial Microsomia [description not available] | 0 | 3.22 | 6 | 0 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 5.52 | 16 | 0 |
Canaliculitis Inflammation and infection of the lacrimal canaliculus area in the LACRIMAL APPARATUS. | 0 | 2.31 | 1 | 0 |
Linear Skull Fracture [description not available] | 0 | 3.99 | 14 | 0 |
Infections, Pseudomonas [description not available] | 0 | 5.86 | 38 | 0 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 5.86 | 38 | 0 |
Obesity A status with BODY WEIGHT that is grossly above the recommended standards, usually due to accumulation of excess FATS in the body. The standards may vary with age, sex, genetic or cultural background. In the BODY MASS INDEX, a BMI greater than 30.0 kg/m2 is considered obese, and a BMI greater than 40.0 kg/m2 is considered morbidly obese (MORBID OBESITY). | 0 | 7.52 | 11 | 1 |
Sunburn An injury to the skin causing erythema, tenderness, and sometimes blistering and resulting from excessive exposure to the sun. The reaction is produced by the ultraviolet radiation in sunlight. | 0 | 6.59 | 8 | 1 |
Leukemia, Pre-B-Cell [description not available] | 0 | 2.59 | 2 | 0 |
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma A leukemia/lymphoma found predominately in children and adolescents and characterized by a high number of lymphoblasts and solid tumor lesions. Frequent sites involve LYMPH NODES, skin, and bones. It most commonly presents as leukemia. | 0 | 2.59 | 2 | 0 |
Fowl Paralysis [description not available] | 0 | 4.26 | 7 | 0 |
Charcot-Bouchard Aneurysm [description not available] | 0 | 2.31 | 1 | 0 |
Adult Neuronal Ceroid Lipofuscinosis [description not available] | 0 | 5.97 | 14 | 0 |
Neuronal Ceroid-Lipofuscinoses A group of severe neurodegenerative diseases characterized by intracellular accumulation of autofluorescent wax-like lipid materials (CEROID; LIPOFUSCIN) in neurons. There are several subtypes based on mutations of the various genes, time of disease onset, and severity of the neurological defects such as progressive DEMENTIA; SEIZURES; and visual failure. | 0 | 5.97 | 14 | 0 |
Viral Zoonoses Viral infections that may be transmitted between non-human animals and HUMANS. | 0 | 2.31 | 1 | 0 |
Cow Pox [description not available] | 0 | 2.58 | 2 | 0 |
Acoustic Neuroma [description not available] | 0 | 3.26 | 6 | 0 |
Abnormalities, Congenital [description not available] | 0 | 8.23 | 93 | 0 |
Amish Brittle Hair Brain Syndrome [description not available] | 0 | 2.31 | 1 | 0 |
Hypercoagulability [description not available] | 0 | 2.79 | 3 | 0 |
Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 2.79 | 3 | 0 |
Multiple Hemangioblastomas [description not available] | 0 | 2.83 | 3 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 3.09 | 5 | 0 |
Angiomatosis Retinae [description not available] | 0 | 3.48 | 8 | 0 |
von Hippel-Lindau Disease An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. | 0 | 3.48 | 8 | 0 |
Hemangioblastoma A benign tumor of the nervous system that may occur sporadically or in association with VON HIPPEL-LINDAU DISEASE. It accounts for approximately 2% of intracranial tumors, arising most frequently in the cerebellar hemispheres and vermis. Histologically, the tumors are composed of multiple capillary and sinusoidal channels lined with endothelial cells and clusters of lipid-laden pseudoxanthoma cells. Usually solitary, these tumors can be multiple and may also occur in the brain stem, spinal cord, retina, and supratentorial compartment. Cerebellar hemangioblastomas usually present in the third decade with INTRACRANIAL HYPERTENSION, and ataxia. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2071-2) | 0 | 2.83 | 3 | 0 |
Alport Syndrome [description not available] | 0 | 4.97 | 9 | 0 |
Nephritis, Hereditary A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE. | 0 | 4.97 | 9 | 0 |
Acrodermatitis Inflammation involving the skin of the extremities, especially the hands and feet. Several forms are known, some idiopathic and some hereditary. The infantile form is called Gianotti-Crosti syndrome. | 0 | 2.42 | 2 | 0 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 7.77 | 45 | 0 |
Lacrimal Duct Obstruction Interference with the secretion of tears by the lacrimal glands. Obstruction of the LACRIMAL SAC or NASOLACRIMAL DUCT causing acute or chronic inflammation of the lacrimal sac (DACRYOCYSTITIS). It is caused also in infants by failure of the nasolacrimal duct to open into the inferior meatus and occurs about the third week of life. In adults occlusion may occur spontaneously or after injury or nasal disease. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p250) | 0 | 3.22 | 6 | 0 |
Infection Reactivation [description not available] | 0 | 2.31 | 1 | 0 |
Paranasal Sinus Diseases Diseases affecting or involving the PARANASAL SINUSES and generally manifesting as inflammation, abscesses, cysts, or tumors. | 0 | 5.21 | 12 | 1 |
ARSB Deficiency [description not available] | 0 | 2.91 | 4 | 0 |
Mucopolysaccharidosis VI Mucopolysaccharidosis with excessive CHONDROITIN SULFATE B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-ACETYLGALACTOSAMINE-4-SULFATASE (arylsulfatase B). | 0 | 2.91 | 4 | 0 |
Infections, Microspora [description not available] | 0 | 3.36 | 2 | 0 |
Ornithosis [description not available] | 0 | 4.59 | 6 | 1 |
Psittacosis Infection with CHLAMYDOPHILA PSITTACI (formerly Chlamydia psittaci), transmitted to humans by inhalation of dust-borne contaminated nasal secretions or excreta of infected BIRDS. This infection results in a febrile illness characterized by PNEUMONITIS and systemic manifestations. | 0 | 9.59 | 6 | 1 |
Benign Neoplasms, Brain [description not available] | 0 | 11.16 | 108 | 1 |
Brain Neoplasms Neoplasms of the intracranial components of the central nervous system, including the cerebral hemispheres, basal ganglia, hypothalamus, thalamus, brain stem, and cerebellum. Brain neoplasms are subdivided into primary (originating from brain tissue) and secondary (i.e., metastatic) forms. Primary neoplasms are subdivided into benign and malignant forms. In general, brain tumors may also be classified by age of onset, histologic type, or presenting location in the brain. | 0 | 11.16 | 108 | 1 |
Choroidal Detachment Separation of the CHOROID from the SCLERA. | 0 | 3.23 | 1 | 0 |
Athletic Injuries Injuries incurred during participation in competitive or non-competitive sports. | 0 | 4.17 | 6 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 2.65 | 3 | 0 |
Bipolar Disorder A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence. | 0 | 2.65 | 3 | 0 |
Siderosis A form of pneumoconiosis resulting from inhalation of iron in the mining dust or welding fumes. | 0 | 9.03 | 15 | 0 |
Dementias, Transmissible [description not available] | 0 | 4.18 | 3 | 0 |
Injuries, Needlestick [description not available] | 0 | 2.93 | 4 | 0 |
Embryopathies [description not available] | 0 | 6.68 | 31 | 0 |
Dwarfism, Growth Hormone Deficiency [description not available] | 0 | 2.67 | 3 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 2.91 | 4 | 0 |
Dwarfism, Pituitary A form of dwarfism caused by complete or partial GROWTH HORMONE deficiency, resulting from either the lack of GROWTH HORMONE-RELEASING FACTOR from the HYPOTHALAMUS or from the mutations in the growth hormone gene (GH1) in the PITUITARY GLAND. It is also known as Type I pituitary dwarfism. Human hypophysial dwarf is caused by a deficiency of HUMAN GROWTH HORMONE during development. | 0 | 2.67 | 3 | 0 |
Hypopituitarism Diminution or cessation of secretion of one or more hormones from the anterior pituitary gland (including LH; FOLLICLE STIMULATING HORMONE; SOMATOTROPIN; and CORTICOTROPIN). This may result from surgical or radiation ablation, non-secretory PITUITARY NEOPLASMS, metastatic tumors, infarction, PITUITARY APOPLEXY, infiltrative or granulomatous processes, and other conditions. | 0 | 2.91 | 4 | 0 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 3.07 | 5 | 0 |
Cerebro-Oculo-Renal Syndrome [description not available] | 0 | 3.34 | 7 | 0 |
Disorder, Borderline Personality [description not available] | 0 | 3.69 | 3 | 0 |
Borderline Personality Disorder A personality disorder marked by a pattern of instability of interpersonal relationships, self-image, and affects, and marked impulsivity beginning by early adulthood and present in a variety of contexts. (DSM-IV) | 0 | 3.69 | 3 | 0 |
Injuries, Soft Tissue [description not available] | 0 | 3.85 | 2 | 0 |
Sinus Infections [description not available] | 0 | 3.89 | 13 | 0 |
Cellulitis, Orbital [description not available] | 0 | 5.03 | 9 | 0 |
Infections, Serratia [description not available] | 0 | 3.82 | 2 | 1 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 10.02 | 16 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 3.89 | 13 | 0 |
Cranial Nerve Diseases Disorders of one or more of the twelve cranial nerves. With the exception of the optic and olfactory nerves, this includes disorders of the brain stem nuclei from which the cranial nerves originate or terminate. | 0 | 5.76 | 15 | 0 |
Tolosa-Hunt Syndrome An idiopathic syndrome characterized by the formation of granulation tissue in the anterior cavernous sinus or superior orbital fissure, producing a painful ophthalmoplegia. (Adams et al., Principles of Neurology, 6th ed, p271) | 0 | 2.15 | 1 | 0 |
Infections, Pneumococcal [description not available] | 0 | 3.38 | 7 | 0 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 3.38 | 7 | 0 |
Aggression Behavior which may be manifested by destructive and attacking action which is verbal or physical, by covert attitudes of hostility or by obstructionism. | 0 | 3.39 | 7 | 0 |
Cannabis Abuse [description not available] | 0 | 3.48 | 2 | 0 |
Marijuana Abuse Use of marijuana associated with abnormal psychological, social, and or occupational functioning. | 0 | 3.48 | 2 | 0 |
Abnormal Karyotype A variation from the normal set of chromosomes characteristic of a species. | 0 | 2.15 | 1 | 0 |
Chromosomal Translocation [description not available] | 0 | 4.91 | 8 | 0 |
Atresia, Esophageal [description not available] | 0 | 2.48 | 2 | 0 |
Esophageal Atresia Congenital abnormality characterized by the lack of full development of the ESOPHAGUS that commonly occurs with TRACHEOESOPHAGEAL FISTULA. Symptoms include excessive SALIVATION; GAGGING; CYANOSIS; and DYSPNEA. | 0 | 2.48 | 2 | 0 |
Osteomyelitis INFLAMMATION of the bone as a result of infection. It may be caused by a variety of infectious agents, especially pyogenic (PUS - producing) BACTERIA. | 0 | 2.66 | 3 | 0 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 3.75 | 11 | 0 |
Purpura Purplish or brownish red discoloration, easily visible through the epidermis, caused by hemorrhage into the tissues. When the size of the discolorization is | 0 | 8.75 | 11 | 0 |
Infections, Klebsiella [description not available] | 0 | 3.11 | 5 | 0 |
Rupture, Spontaneous Tear or break of an organ, vessel or other soft part of the body, occurring in the absence of external force. | 0 | 4.67 | 11 | 0 |
Klebsiella Infections Infections with bacteria of the genus KLEBSIELLA. | 0 | 3.11 | 5 | 0 |
Granulomas [description not available] | 0 | 12.14 | 50 | 0 |
Infections, Mycobacterium [description not available] | 0 | 3.36 | 7 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 7.14 | 50 | 0 |
Mycobacterium Infections Infections with bacteria of the genus MYCOBACTERIUM. | 0 | 3.36 | 7 | 0 |
Lymphatic Abnormalities Congenital or acquired structural abnormalities of the lymphatic system (LYMPHOID TISSUE) including the lymph vessels. | 0 | 2.17 | 1 | 0 |
Vascular Malformations A spectrum of congenital, inherited, or acquired abnormalities in BLOOD VESSELS that can adversely affect the normal blood flow in ARTERIES or VEINS. Most are congenital defects such as abnormal communications between blood vessels (fistula), shunting of arterial blood directly into veins bypassing the CAPILLARIES (arteriovenous malformations), formation of large dilated blood blood-filled vessels (cavernous angioma), and swollen capillaries (capillary telangiectases). In rare cases, vascular malformations can result from trauma or diseases. | 0 | 4.29 | 7 | 0 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 3.63 | 3 | 0 |
Sinusitis, Sphenoid [description not available] | 0 | 2.78 | 3 | 0 |
Anterior Cervical Pain [description not available] | 0 | 2.15 | 1 | 0 |
Neck Pain Discomfort or more intense forms of pain that are localized to the cervical region. This term generally refers to pain in the posterior or lateral regions of the neck. | 0 | 7.15 | 1 | 0 |
Shoulder Pain Unilateral or bilateral pain of the shoulder. It is often caused by physical activities such as work or sports participation, but may also be pathologic in origin. | 0 | 2.15 | 1 | 0 |
Infection [description not available] | 0 | 13.29 | 50 | 0 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 8.29 | 50 | 0 |
Xerophthalmia Dryness of the eye surfaces caused by deficiency of tears or conjunctival secretions. It may be associated with vitamin A deficiency, trauma, or any condition in which the eyelids do not close completely. | 0 | 13.93 | 29 | 3 |
Asialia [description not available] | 0 | 6.17 | 5 | 1 |
Xerostomia Decreased salivary flow. | 0 | 6.17 | 5 | 1 |
Synkinesis An involuntary movement accompanying a volitional movement. It often refers to facial movements that accompany FACIAL PARALYSIS. | 0 | 4.42 | 8 | 0 |
Allergic Rhinitis [description not available] | 0 | 5.09 | 6 | 0 |
Asthma, Bronchial [description not available] | 0 | 9.83 | 31 | 1 |
Asthma A form of bronchial disorder with three distinct components: airway hyper-responsiveness (RESPIRATORY HYPERSENSITIVITY), airway INFLAMMATION, and intermittent AIRWAY OBSTRUCTION. It is characterized by spasmodic contraction of airway smooth muscle, WHEEZING, and dyspnea (DYSPNEA, PAROXYSMAL). | 0 | 14.83 | 31 | 1 |
Rhinitis, Allergic An inflammation of the NASAL MUCOSA triggered by ALLERGENS. | 0 | 5.09 | 6 | 0 |
Metastase [description not available] | 0 | 10.48 | 42 | 1 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 10.48 | 42 | 1 |
Cancer, Radiation-Induced [description not available] | 0 | 8.05 | 36 | 0 |
Atheroembolism [description not available] | 0 | 3.86 | 4 | 0 |
Embolism, Cholesterol Blocking of a blood vessel by CHOLESTEROL-rich atheromatous deposits, generally occurring in the flow from a large artery to small arterial branches. It is also called arterial-arterial embolization or atheroembolism which may be spontaneous or iatrogenic. Patients with spontaneous atheroembolism often have painful, cyanotic digits of acute onset. | 0 | 3.86 | 4 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 7.54 | 23 | 1 |
Extranodal NK-T-Cell Lymphoma [description not available] | 0 | 3.09 | 1 | 0 |
Lymphoma, Non-Hodgkin Any of a group of malignant tumors of lymphoid tissue that differ from HODGKIN DISEASE, being more heterogeneous with respect to malignant cell lineage, clinical course, prognosis, and therapy. The only common feature among these tumors is the absence of giant REED-STERNBERG CELLS, a characteristic of Hodgkin's disease. | 0 | 7.54 | 23 | 1 |
Shingles [description not available] | 0 | 6.4 | 42 | 0 |
Herpes Zoster An acute infectious, usually self-limited, disease believed to represent activation of latent varicella-zoster virus (HERPESVIRUS 3, HUMAN) in those who have been rendered partially immune after a previous attack of CHICKENPOX. It involves the SENSORY GANGLIA and their areas of innervation and is characterized by severe neuralgic pain along the distribution of the affected nerve and crops of clustered vesicles over the area. (From Dorland, 27th ed) | 0 | 11.4 | 42 | 0 |
Periphlebitis Periphlebitis is inflammation of the outer coat of a vein or of tissues surrounding the vein. | 0 | 4.02 | 15 | 0 |
Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). | 0 | 4.02 | 15 | 0 |
Smoking Cessation Discontinuing the habit of SMOKING. | 0 | 3.42 | 2 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 6.39 | 30 | 0 |
Astrocytosis [description not available] | 0 | 4.92 | 8 | 0 |
Chronic Insomnia [description not available] | 0 | 4.89 | 4 | 2 |
Sleep Initiation and Maintenance Disorders Disorders characterized by impairment of the ability to initiate or maintain sleep. This may occur as a primary disorder or in association with another medical or psychiatric condition. | 0 | 4.89 | 4 | 2 |
Neuroblastoma A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51) | 0 | 4.61 | 10 | 0 |
Space Adaptation Syndrome [description not available] | 0 | 3.09 | 1 | 0 |
Devic Disease [description not available] | 0 | 4.19 | 18 | 0 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 9.53 | 114 | 1 |
Neuromyelitis Optica A syndrome characterized by acute OPTIC NEURITIS; MYELITIS, TRANSVERSE; demyelinating and/or necrotizing lesions in the OPTIC NERVES and SPINAL CORD; and presence of specific autoantibodies to AQUAPORIN 4. | 0 | 4.19 | 18 | 0 |
Protein Aggregation, Pathological A biochemical phenomenon in which misfolded proteins aggregate either intra- or extracellularly. Triggered by factors such as MUTATION; POST-TRANSLATIONAL MODIFICATIONS, and environmental stress, it is generally associated with ALZHEIMER DISEASE; PARKINSON DISEASE; HUNTINGTON DISEASE; and TYPE 2 DIABETES MELLITUS. | 0 | 3.74 | 3 | 0 |
Bernard Syndrome [description not available] | 0 | 6.24 | 25 | 0 |
Cancer of Head [description not available] | 0 | 15.48 | 45 | 27 |
Head and Neck Neoplasms Soft tissue tumors or cancer arising from the mucosal surfaces of the LIP; oral cavity; PHARYNX; LARYNX; and cervical esophagus. Other sites included are the NOSE and PARANASAL SINUSES; SALIVARY GLANDS; THYROID GLAND and PARATHYROID GLANDS; and MELANOMA and non-melanoma skin cancers of the head and neck. (from Holland et al., Cancer Medicine, 4th ed, p1651) | 0 | 15.48 | 45 | 27 |
Cerebral Palsy, Athetoid [description not available] | 0 | 5.2 | 12 | 1 |
Bronchopulmonary Dysplasia A chronic lung disease developed after OXYGEN INHALATION THERAPY or mechanical ventilation (VENTILATION, MECHANICAL) usually occurring in certain premature infants (INFANT, PREMATURE) or newborn infants with respiratory distress syndrome (RESPIRATORY DISTRESS SYNDROME, NEWBORN). Histologically, it is characterized by the unusual abnormalities of the bronchioles, such as METAPLASIA, decrease in alveolar number, and formation of CYSTS. | 0 | 4.31 | 4 | 1 |
Cerebral Palsy A heterogeneous group of nonprogressive motor disorders caused by chronic brain injuries that originate in the prenatal period, perinatal period, or first few years of life. The four major subtypes are spastic, athetoid, ataxic, and mixed cerebral palsy, with spastic forms being the most common. The motor disorder may range from difficulties with fine motor control to severe spasticity (see MUSCLE SPASTICITY) in all limbs. Spastic diplegia (Little disease) is the most common subtype, and is characterized by spasticity that is more prominent in the legs than in the arms. Pathologically, this condition may be associated with LEUKOMALACIA, PERIVENTRICULAR. (From Dev Med Child Neurol 1998 Aug;40(8):520-7) | 0 | 10.2 | 12 | 1 |
Fasciculation Involuntary contraction of the muscle fibers innervated by a motor unit. Fasciculations may be visualized as a muscle twitch or dimpling under the skin, but usually do not generate sufficient force to move a limb. They may represent a benign condition or occur as a manifestation of MOTOR NEURON DISEASE or PERIPHERAL NERVOUS SYSTEM DISEASES. (Adams et al., Principles of Neurology, 6th ed, p1294) | 0 | 7.7 | 3 | 0 |
Arthropathies [description not available] | 0 | 3.34 | 7 | 0 |
Joint Diseases Diseases involving the JOINTS. | 0 | 3.34 | 7 | 0 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 7.23 | 23 | 1 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 7.23 | 23 | 1 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 5.34 | 13 | 1 |
Cerebral Infarction The formation of an area of NECROSIS in the CEREBRUM caused by an insufficiency of arterial or venous blood flow. Infarcts of the cerebrum are generally classified by hemisphere (i.e., left vs. right), lobe (e.g., frontal lobe infarction), arterial distribution (e.g., INFARCTION, ANTERIOR CEREBRAL ARTERY), and etiology (e.g., embolic infarction). | 0 | 10.34 | 13 | 1 |
Electron Transport Chain Deficiencies, Mitochondrial [description not available] | 0 | 7.23 | 8 | 0 |
Mitochondrial Diseases Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes. | 0 | 7.23 | 8 | 0 |
Nerve Degeneration Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways. | 0 | 7.98 | 69 | 0 |
Dystonia An attitude or posture due to the co-contraction of agonists and antagonist muscles in one region of the body. It most often affects the large axial muscles of the trunk and limb girdles. Conditions which feature persistent or recurrent episodes of dystonia as a primary manifestation of disease are referred to as DYSTONIC DISORDERS. (Adams et al., Principles of Neurology, 6th ed, p77) | 0 | 3.4 | 7 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 6.84 | 15 | 1 |
Complications, Pregnancy [description not available] | 0 | 7.52 | 29 | 0 |
Airway Hyper-Responsiveness [description not available] | 0 | 2.66 | 3 | 0 |
Breathing Sounds [description not available] | 0 | 3.39 | 2 | 0 |
Nasal Catarrh [description not available] | 0 | 6.06 | 11 | 0 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 3.39 | 2 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 11.06 | 11 | 0 |
Gambling, Pathologic [description not available] | 0 | 2.78 | 3 | 0 |
Gambling An activity distinguished primarily by an element of risk in trying to obtain a desired goal, e.g., playing a game of chance for money. | 0 | 7.78 | 3 | 0 |
Biological Clock Disturbances [description not available] | 0 | 2.54 | 2 | 0 |
Apraxia [description not available] | 0 | 7.86 | 4 | 0 |
Apraxias A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7) | 0 | 2.86 | 4 | 0 |
Adult Neuroaxonal Dystrophy [description not available] | 0 | 2.67 | 3 | 0 |
Degenerative Disease, Nervous System, Hereditary [description not available] | 0 | 2.17 | 1 | 0 |
Cervical Dystonia A common form of DYSTONIA due to involuntary sustained or spasmodic, repetitive muscle contractions in the neck region. According to the position of the twisted neck and head, cervical dystonia can be categorized as torticollis, laterocollis, retrocollis, and a combination of these abnormal postures. | 0 | 3.48 | 8 | 0 |
Iron Metabolism Disorders Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization. (From Mosby's Medical, Nursing, & Allied Health Dictionary, 4th ed) | 0 | 2.67 | 3 | 0 |
Torticollis A symptom, not a disease, of a twisted neck. In most instances, the head is tipped toward one side and the chin rotated toward the other. The involuntary muscle contractions in the neck region of patients with torticollis can be due to congenital defects, trauma, inflammation, tumors, and neurological or other factors. | 0 | 3.48 | 8 | 0 |
Buerger Disease [description not available] | 0 | 3.19 | 6 | 0 |
Central Nervous System Lupus [description not available] | 0 | 3.09 | 1 | 0 |
Anorexia Nervosa An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 7.17 | 1 | 0 |
Acoustic Trauma Usually refer to hearing loss due to a single noise event such as an explosion or shotgun blast. | 0 | 2.41 | 2 | 0 |
Hearing Loss, Noise-Induced Hearing loss due to exposure to explosive loud noise or chronic exposure to sound level greater than 85 dB. The hearing loss is often in the frequency range 4000-6000 hertz. | 0 | 2.41 | 2 | 0 |
Abscess, Amebic [description not available] | 0 | 3.57 | 9 | 0 |
Amebiasis Infection with any of various amebae. It is an asymptomatic carrier state in most individuals, but diseases ranging from chronic, mild diarrhea to fulminant dysentery may occur. | 0 | 8.57 | 9 | 0 |
Respiration Disorders Diseases of the respiratory system in general or unspecified or for a specific respiratory disease not available. | 0 | 3.23 | 6 | 0 |
Tonsillitis Inflammation of the tonsils, especially the PALATINE TONSILS but the ADENOIDS (pharyngeal tonsils) and lingual tonsils may also be involved. Tonsillitis usually is caused by bacterial infection. Tonsillitis may be acute, chronic, or recurrent. | 0 | 8.04 | 5 | 0 |
Creeping Eruption [description not available] | 0 | 3.37 | 7 | 0 |
Infective Endocarditis [description not available] | 0 | 3.57 | 3 | 0 |
Infections, Prosthesis-Related [description not available] | 0 | 3.09 | 1 | 0 |
Endocarditis Inflammation of the inner lining of the heart (ENDOCARDIUM), the continuous membrane lining the four chambers and HEART VALVES. It is often caused by microorganisms including bacteria, viruses, fungi, and rickettsiae. Left untreated, endocarditis can damage heart valves and become life-threatening. | 0 | 3.57 | 3 | 0 |
Eyelid Diseases Diseases involving the EYELIDS. | 0 | 10.93 | 67 | 1 |
Macroglossia The presence of an excessively large tongue, which may be congenital or may develop as a result of a tumor or edema due to obstruction of lymphatic vessels, or it may occur in association with hyperpituitarism or acromegaly. It also may be associated with malocclusion because of pressure of the tongue on the teeth. (From Jablonski, Dictionary of Dentistry, 1992) | 0 | 2.52 | 2 | 0 |
AL Amyloidosis [description not available] | 0 | 2.64 | 3 | 0 |
Immunoglobulin Light-chain Amyloidosis A nonproliferative disorder of the PLASMA CELL characterized by excessive production and misfolding of IMMUNOGLOBULIN LIGHT CHAINS that form insoluble amyloid fibrils (see AMYLOID DEPOSITS) in various tissues. Clinical features include LIVER FAILURE; MULTIPLE MYELOMA; NEPHROTIC SYNDROME; RESTRICTIVE CARDIOMYOPATHY, and neuropathies. | 0 | 2.64 | 3 | 0 |
Neoplasms, Nervous System [description not available] | 0 | 2.41 | 2 | 0 |
Cancer of Pituitary [description not available] | 0 | 5.77 | 36 | 0 |
Blood Vessel Tumors [description not available] | 0 | 2.17 | 1 | 0 |
Pituitary Neoplasms Neoplasms which arise from or metastasize to the PITUITARY GLAND. The majority of pituitary neoplasms are adenomas, which are divided into non-secreting and secreting forms. Hormone producing forms are further classified by the type of hormone they secrete. Pituitary adenomas may also be characterized by their staining properties (see ADENOMA, BASOPHIL; ADENOMA, ACIDOPHIL; and ADENOMA, CHROMOPHOBE). Pituitary tumors may compress adjacent structures, including the HYPOTHALAMUS, several CRANIAL NERVES, and the OPTIC CHIASM. Chiasmal compression may result in bitemporal HEMIANOPSIA. | 0 | 5.77 | 36 | 0 |
Vasculitis, Retinal [description not available] | 0 | 4.44 | 8 | 0 |
Retinal Vasculitis Inflammation of the retinal vasculature with various causes including infectious disease; LUPUS ERYTHEMATOSUS, SYSTEMIC; MULTIPLE SCLEROSIS; BEHCET SYNDROME; and CHORIORETINITIS. | 0 | 4.44 | 8 | 0 |
Infections, Orthomyxoviridae [description not available] | 0 | 3.8 | 11 | 0 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 3.8 | 11 | 0 |
Black Fever [description not available] | 0 | 2.88 | 4 | 0 |
Leishmaniasis, American [description not available] | 0 | 2.88 | 4 | 0 |
Leishmaniasis, Visceral A chronic disease caused by LEISHMANIA DONOVANI and transmitted by the bite of several sandflies of the genera Phlebotomus and Lutzomyia. It is commonly characterized by fever, chills, vomiting, anemia, hepatosplenomegaly, leukopenia, hypergammaglobulinemia, emaciation, and an earth-gray color of the skin. The disease is classified into three main types according to geographic distribution: Indian, Mediterranean (or infantile), and African. | 0 | 2.88 | 4 | 0 |
Leishmaniasis, Cutaneous An endemic disease that is characterized by the development of single or multiple localized lesions on exposed areas of skin that typically ulcerate. The disease has been divided into Old and New World forms. Old World leishmaniasis is separated into three distinct types according to epidemiology and clinical manifestations and is caused by species of the L. tropica and L. aethiopica complexes as well as by species of the L. major genus. New World leishmaniasis, also called American leishmaniasis, occurs in South and Central America and is caused by species of the L. mexicana or L. braziliensis complexes. | 0 | 2.88 | 4 | 0 |
Myofibroma A benign tumor that consists chiefly of fibrous CONNECTIVE TISSUE, with variable numbers of MUSCLE CELLS forming portions of the neoplasm (From Stedman's, 27th ed). | 0 | 2.17 | 1 | 0 |
Epilepsy Progressive Myoclonic 2 [description not available] | 0 | 2.17 | 1 | 0 |
Capsule Opacification Clouding or loss of transparency of the posterior lens capsule, usually following CATARACT extraction. | 0 | 2.38 | 2 | 0 |
Frontotemporal Lobar Degeneration Heterogeneous group of neurodegenerative disorders characterized by frontal and temporal lobe atrophy associated with neuronal loss, gliosis, and dementia. Patients exhibit progressive changes in social, behavioral, and/or language function. Multiple subtypes or forms are recognized based on presence or absence of TAU PROTEIN inclusions. FTLD includes three clinical syndromes: FRONTOTEMPORAL DEMENTIA, semantic dementia, and PRIMARY PROGRESSIVE NONFLUENT APHASIA. | 0 | 2.58 | 2 | 0 |
Facial Asymmetry Congenital or acquired asymmetry of the face. | 0 | 9.61 | 26 | 0 |
Marburg Disease [description not available] | 0 | 2.17 | 1 | 0 |
Marburg Virus Disease An RNA virus infection of rhesus, vervet, and squirrel monkeys transmissible to man. | 0 | 2.17 | 1 | 0 |
C gattii Infection [description not available] | 0 | 4.89 | 14 | 0 |
Multifocal Choroiditis A multifocal uveitis syndrome involving the RETINAL PIGMENT EPITHELIUM and capillary layer of the CHOROID. It is characterized by chronic UVEITIS and multiple CHOROID lesions referred to as white dots, blurry vision, floaters, sensitivity to light, blind spots, and eye discomfort. | 0 | 2.21 | 1 | 0 |
Choroiditis Inflammation of the choroid. | 0 | 4.43 | 23 | 0 |
Cryptococcosis Fungal infection caused by genus CRYPTOCOCCUS. | 0 | 4.89 | 14 | 0 |
Hemorrhagic Disease of Newborn Neonatal nasogastric or intracranial hemorrhage caused by vitamin K deficiency. | 0 | 2.21 | 1 | 0 |
Fibroid [description not available] | 0 | 2.87 | 4 | 0 |
Emphysema, Subcutaneous [description not available] | 0 | 4.13 | 5 | 0 |
Leiomyoma A benign tumor derived from smooth muscle tissue, also known as a fibroid tumor. They rarely occur outside of the UTERUS and the GASTROINTESTINAL TRACT but can occur in the SKIN and SUBCUTANEOUS TISSUE, probably arising from the smooth muscle of small blood vessels in these tissues. | 0 | 2.87 | 4 | 0 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 4.64 | 10 | 0 |
Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | 0 | 4.64 | 10 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 8.04 | 76 | 0 |
Contact Dermatitis [description not available] | 0 | 7.29 | 35 | 0 |
Dermatitis, Contact A type of acute or chronic skin reaction in which sensitivity is manifested by reactivity to materials or substances coming in contact with the skin. It may involve allergic or non-allergic mechanisms. | 0 | 7.29 | 35 | 0 |
Disc, Herniated [description not available] | 0 | 2.17 | 1 | 0 |
Intervertebral Disc Displacement An INTERVERTEBRAL DISC in which the NUCLEUS PULPOSUS has protruded through surrounding ANNULUS FIBROSUS. This occurs most frequently in the lower lumbar region. | 0 | 2.17 | 1 | 0 |
Scalp Dermatoses Skin diseases involving the SCALP. | 0 | 3.3 | 2 | 0 |
Ectropion The turning outward (eversion) of the edge of the eyelid, resulting in the exposure of the palpebral conjunctiva. (Dorland, 27th ed) | 0 | 4.86 | 8 | 0 |
Cranial Nerve VII Injuries [description not available] | 0 | 3.81 | 4 | 0 |
Autosomal Dominant Striatonigral Degeneration [description not available] | 0 | 3.14 | 5 | 0 |
Machado-Joseph Disease A dominantly-inherited ATAXIA first described in people of Azorean and Portuguese descent, and subsequently identified in Brazil, Japan, China, and Australia. This disorder is classified as one of the SPINOCEREBELLAR ATAXIAS (Type 3) and has been associated with a mutation of the MJD1 gene on chromosome 14. Clinical features include progressive ataxia, DYSARTHRIA, postural instability, nystagmus, eyelid retraction, and facial FASCICULATIONS. DYSTONIA is prominent in younger patients (referred to as Type I Machado-Joseph Disease). Type II features ataxia and ocular signs; Type III features MUSCULAR ATROPHY and a sensorimotor neuropathy; and Type IV features extrapyramidal signs combined with a sensorimotor neuropathy. (From Clin Neurosci 1995;3(1):17-22; Ann Neurol 1998 Mar;43(3):288-96) | 0 | 3.14 | 5 | 0 |
Coarctation of Aorta [description not available] | 0 | 2.66 | 3 | 0 |
Angioma A vascular anomaly due to proliferation of blood or lymphatic vessels that forms a tumor-like mass. Vessels in the angioma may or may not be dilated. | 0 | 13.42 | 45 | 1 |
Neurocutaneous Disorders [description not available] | 0 | 4.49 | 9 | 0 |
Aortic Coarctation A birth defect characterized by the narrowing of the AORTA that can be of varying degree and at any point from the transverse arch to the iliac bifurcation. Aortic coarctation causes arterial HYPERTENSION before the point of narrowing and arterial HYPOTENSION beyond the narrowed portion. | 0 | 2.66 | 3 | 0 |
Hemangioma A vascular anomaly due to proliferation of BLOOD VESSELS that forms a tumor-like mass. The common types involve CAPILLARIES and VEINS. It can occur anywhere in the body but is most frequently noticed in the SKIN and SUBCUTANEOUS TISSUE. (from Stedman, 27th ed, 2000) | 0 | 13.42 | 45 | 1 |
Bowel Diseases, Inflammatory [description not available] | 0 | 3.09 | 1 | 0 |
Inflammatory Bowel Diseases Chronic, non-specific inflammation of the GASTROINTESTINAL TRACT. Etiology may be genetic or environmental. This term includes CROHN DISEASE and ULCERATIVE COLITIS. | 0 | 3.09 | 1 | 0 |
Infections, Meningococcal [description not available] | 0 | 2.39 | 2 | 0 |
Meningococcal Infections Infections with bacteria of the species NEISSERIA MENINGITIDIS. | 0 | 2.39 | 2 | 0 |
Carcinogenesis The origin, production or development of cancer through genotypic and phenotypic changes which upset the normal balance between cell proliferation and cell death. Carcinogenesis generally requires a constellation of steps, which may occur quickly or over a period of many years. | 0 | 4.63 | 5 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 6.26 | 34 | 0 |
Central Nervous System Syphilis [description not available] | 0 | 5.77 | 22 | 0 |
Schistosoma japonicum Infection [description not available] | 0 | 2.17 | 1 | 0 |
Left Ventricular Dysfunction [description not available] | 0 | 2.17 | 1 | 0 |
Ventricular Dysfunction, Left A condition in which the LEFT VENTRICLE of the heart was functionally impaired. This condition usually leads to HEART FAILURE; MYOCARDIAL INFARCTION; and other cardiovascular complications. Diagnosis is made by measuring the diminished ejection fraction and a depressed level of motility of the left ventricular wall. | 0 | 2.17 | 1 | 0 |
CJD (Creutzfeldt-Jakob Disease) [description not available] | 0 | 2.7 | 3 | 0 |
Creutzfeldt-Jakob Syndrome A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27)) | 0 | 2.7 | 3 | 0 |
Allergic Contact Dermatitis [description not available] | 0 | 8.81 | 11 | 0 |
Dermatitis, Eczematous [description not available] | 0 | 4.66 | 11 | 0 |
Eczema A pruritic papulovesicular dermatitis occurring as a reaction to many endogenous and exogenous agents (Dorland, 27th ed). | 0 | 4.66 | 11 | 0 |
Dermatitis, Allergic Contact A contact dermatitis due to allergic sensitization to various substances. These substances subsequently produce inflammatory reactions in the skin of those who have acquired hypersensitivity to them as a result of prior exposure. | 0 | 3.81 | 11 | 0 |
Stunted Growth [description not available] | 0 | 5.13 | 18 | 0 |
Primate Diseases Diseases of animals within the order PRIMATES. This term includes diseases of Haplorhini and Strepsirhini. | 0 | 2.44 | 2 | 0 |
Growth Disorders Deviations from the average values for a specific age and sex in any or all of the following: height, weight, skeletal proportions, osseous development, or maturation of features. Included here are both acceleration and retardation of growth. | 0 | 5.13 | 18 | 0 |
Primary Peritonitis [description not available] | 0 | 2.41 | 2 | 0 |
Gastroenteritis INFLAMMATION of any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. Causes of gastroenteritis are many including genetic, infection, HYPERSENSITIVITY, drug effects, and CANCER. | 0 | 2.9 | 4 | 0 |
Peritonitis INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. | 0 | 2.41 | 2 | 0 |
Lymph Node Metastasis [description not available] | 0 | 3.35 | 7 | 0 |
Poisoning, Lead [description not available] | 0 | 4.82 | 13 | 0 |
Lead Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of LEAD or lead compounds. | 0 | 4.82 | 13 | 0 |
Granular Cell Myoblastoma [description not available] | 0 | 2.17 | 1 | 0 |
Autosomal Dominant Myotubular Myopathy [description not available] | 0 | 2.21 | 1 | 0 |
Thrombocytopathy [description not available] | 0 | 3.58 | 3 | 0 |
Blood Platelet Disorders Disorders caused by abnormalities in platelet count or function. | 0 | 3.58 | 3 | 0 |
Hyperlipemia [description not available] | 0 | 6.12 | 12 | 1 |
Long Sleeper Syndrome [description not available] | 0 | 2.65 | 3 | 0 |
Blepharospasm Excessive winking; tonic or clonic spasm of the orbicularis oculi muscle. | 0 | 3.49 | 8 | 0 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 6.12 | 12 | 1 |
Sleep Wake Disorders Abnormal sleep-wake schedule or pattern associated with the CIRCADIAN RHYTHM which affect the length, timing, and/or rigidity of the sleep-wake cycle relative to the day-night cycle. | 0 | 2.65 | 3 | 0 |
Acute Post-Traumatic Stress Disorder [description not available] | 0 | 2.53 | 2 | 0 |
Stress Disorders, Post-Traumatic A class of traumatic stress disorders with symptoms that last more than one month. | 0 | 2.53 | 2 | 0 |
Ovine Diseases [description not available] | 0 | 4.43 | 22 | 0 |
Caprine Diseases [description not available] | 0 | 3.81 | 11 | 0 |
Menopause The last menstrual period. Permanent cessation of menses (MENSTRUATION) is usually defined after 6 to 12 months of AMENORRHEA in a woman over 45 years of age. In the United States, menopause generally occurs in women between 48 and 55 years of age. | 0 | 10.77 | 8 | 1 |
Genetic Diseases [description not available] | 0 | 4.11 | 3 | 0 |
Genetic Diseases, Inborn Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. | 0 | 4.11 | 3 | 0 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 9.12 | 38 | 1 |
Buphthalmos [description not available] | 0 | 6.02 | 46 | 0 |
Atypical Mycobacterial Infection, Disseminated [description not available] | 0 | 4.08 | 5 | 0 |
Acquired Facial Neuropathy [description not available] | 0 | 3.45 | 2 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 4.08 | 16 | 0 |
Waldenstrom Macroglobulinemia A lymphoproliferative disorder characterized by pleomorphic B-LYMPHOCYTES including PLASMA CELLS, with increased levels of monoclonal serum IMMUNOGLOBULIN M. There is lymphoplasmacytic cells infiltration into bone marrow and often other tissues, also known as lymphoplasmacytic lymphoma. Clinical features include ANEMIA; HEMORRHAGES; and hyperviscosity. | 0 | 9.08 | 16 | 0 |
Myoclonic Jerk [description not available] | 0 | 4.8 | 13 | 0 |
Audiogenic Epilepsy [description not available] | 0 | 4.21 | 3 | 0 |
Epilepsy, Reflex A subtype of epilepsy characterized by seizures that are consistently provoked by a certain specific stimulus. Auditory, visual, and somatosensory stimuli as well as the acts of writing, reading, eating, and decision making are examples of events or activities that may induce seizure activity in affected individuals. (From Neurol Clin 1994 Feb;12(1):57-8) | 0 | 4.21 | 3 | 0 |
Muscle Disorders [description not available] | 0 | 4.52 | 25 | 0 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 5.01 | 16 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 4.52 | 25 | 0 |
Cancer of Intestines [description not available] | 0 | 2.39 | 2 | 0 |
Cancer of Pancreas [description not available] | 0 | 2.67 | 3 | 0 |
Cancer of Stomach [description not available] | 0 | 2.67 | 3 | 0 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 2.39 | 2 | 0 |
Pancreatic Neoplasms Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA). | 0 | 2.67 | 3 | 0 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 2.67 | 3 | 0 |
Disease A definite pathologic process with a characteristic set of signs and symptoms. It may affect the whole body or any of its parts, and its etiology, pathology, and prognosis may be known or unknown. | 0 | 9.65 | 645 | 0 |
Polyps Discrete abnormal tissue masses that protrude into the lumen of the DIGESTIVE TRACT or the RESPIRATORY TRACT. Polyps can be spheroidal, hemispheroidal, or irregular mound-shaped structures attached to the MUCOUS MEMBRANE of the lumen wall either by a stalk, pedunculus, or by a broad base. | 0 | 2.21 | 1 | 0 |
HMN (Hereditary Motor Neuropathy) Proximal Type I [description not available] | 0 | 2.21 | 1 | 0 |
Spinal Muscular Atrophies of Childhood A group of recessive inherited diseases that feature progressive muscular atrophy and hypotonia. They are classified as type I (Werdnig-Hoffman disease), type II (intermediate form), and type III (Kugelberg-Welander disease). Type I is fatal in infancy, type II has a late infantile onset and is associated with survival into the second or third decade. Type III has its onset in childhood, and is slowly progressive. (J Med Genet 1996 Apr:33(4):281-3) | 0 | 2.21 | 1 | 0 |
Hypertelorism Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid. | 0 | 10.42 | 15 | 0 |
Encephalitozoonosis Infection with FUNGI of the genus ENCEPHALITOZOON. Lesions commonly occur in the BRAIN and KIDNEY tubules. Other sites of infection in MAMMALS are the LIVER; ADRENAL GLANDS; OPTIC NERVES; RETINA; and MYOCARDIUM. | 0 | 3.42 | 2 | 0 |
Toxocariasis Infection by round worms of the genus TOXOCARA, usually found in wild and domesticated cats and dogs and foxes, except for the larvae, which may produce visceral and ocular larva migrans in man. | 0 | 11.17 | 23 | 0 |
Polysyndactyly [description not available] | 0 | 3.47 | 8 | 0 |
Infarct, Lacunar [description not available] | 0 | 2.61 | 2 | 0 |
Infusion Site Adverse Event [description not available] | 0 | 4.51 | 1 | 1 |
Fra(X) Syndrome [description not available] | 0 | 3.75 | 10 | 0 |
Fragile X Syndrome A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226) | 0 | 8.75 | 10 | 0 |
Convulsions, Grand Mal [description not available] | 0 | 3.22 | 6 | 0 |
Epilepsy, Tonic-Clonic A generalized seizure disorder characterized by recurrent major motor seizures. The initial brief tonic phase is marked by trunk flexion followed by diffuse extension of the trunk and extremities. The clonic phase features rhythmic flexor contractions of the trunk and limbs, pupillary dilation, elevations of blood pressure and pulse, urinary incontinence, and tongue biting. This is followed by a profound state of depressed consciousness (post-ictal state) which gradually improves over minutes to hours. The disorder may be cryptogenic, familial, or symptomatic (caused by an identified disease process). (From Adams et al., Principles of Neurology, 6th ed, p329) | 0 | 3.22 | 6 | 0 |
Pyoderma Gangrenosum An idiopathic, rapidly evolving, and severely debilitating disease occurring most commonly in association with chronic ulcerative colitis. It is characterized by the presence of boggy, purplish ulcers with undermined borders, appearing mostly on the legs. The majority of cases are in people between 40 and 60 years old. Its etiology is unknown. | 0 | 3.12 | 1 | 0 |
Acute Febrile Neutrophilic Dermatosis [description not available] | 0 | 3.39 | 2 | 0 |
Aphakia Absence of crystalline lens totally or partially from field of vision, from any cause except after cataract extraction. Aphakia is mainly congenital or as result of LENS DISLOCATION AND SUBLUXATION. | 0 | 8.12 | 37 | 1 |
Myoepithelial Tumor [description not available] | 0 | 2.21 | 1 | 0 |
Myoepithelioma A usually benign tumor made up predominantly of myoepithelial cells. | 0 | 2.21 | 1 | 0 |
Dysphagia [description not available] | 0 | 3.64 | 3 | 0 |
Nasal Bleeding [description not available] | 0 | 3.97 | 5 | 0 |
Diffuse Myofascial Pain Syndrome [description not available] | 0 | 8.71 | 6 | 4 |
Deglutition Disorders Difficulty in SWALLOWING which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the PHARYNX and UPPER ESOPHAGEAL SPHINCTER; and esophageal dysphagia due to malfunction of the ESOPHAGUS. | 0 | 3.64 | 3 | 0 |
Epistaxis Bleeding from the nose. | 0 | 3.97 | 5 | 0 |
Fibromyalgia A common nonarticular rheumatic syndrome characterized by myalgia and multiple points of focal muscle tenderness to palpation (trigger points). Muscle pain is typically aggravated by inactivity or exposure to cold. This condition is often associated with general symptoms, such as sleep disturbances, fatigue, stiffness, HEADACHES, and occasionally DEPRESSION. There is significant overlap between fibromyalgia and the chronic fatigue syndrome (FATIGUE SYNDROME, CHRONIC). Fibromyalgia may arise as a primary or secondary disease process. It is most frequent in females aged 20 to 50 years. (From Adams et al., Principles of Neurology, 6th ed, p1494-95) | 0 | 8.71 | 6 | 4 |
Eye Hemorrhage Intraocular hemorrhage from the vessels of various tissues of the eye. | 0 | 7.68 | 27 | 1 |
Acid beta-Glucosidase Deficiency [description not available] | 0 | 3.45 | 2 | 0 |
Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement. | 0 | 8.45 | 2 | 0 |
Agnosia for Faces [description not available] | 0 | 3.47 | 7 | 0 |
Classic Globoid Cell Leukodystrophy [description not available] | 0 | 2.38 | 2 | 0 |
Leukodystrophy, Globoid Cell An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such as GALACTOSYLCERAMIDES and PSYCHOSINE. It is characterized by demyelination associated with large multinucleated globoid cells, predominantly involving the white matter of the central nervous system. The loss of MYELIN disrupts normal conduction of nerve impulses. | 0 | 2.38 | 2 | 0 |
Coma A profound state of unconsciousness associated with depressed cerebral activity from which the individual cannot be aroused. Coma generally occurs when there is dysfunction or injury involving both cerebral hemispheres or the brain stem RETICULAR FORMATION. | 0 | 11.14 | 12 | 1 |
Retinocochleocerebral Vasculopathy [description not available] | 0 | 2.57 | 2 | 0 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 3.33 | 2 | 0 |
Pulmonary Hypertension [description not available] | 0 | 9.43 | 8 | 4 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 5.05 | 7 | 0 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 3.33 | 2 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 9.43 | 8 | 4 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 5.05 | 7 | 0 |
Coats Disease [description not available] | 0 | 2.21 | 1 | 0 |
Retinal Telangiectasis A group of rare, idiopathic, congenital retinal vascular anomalies affecting the retinal capillaries. It is characterized by dilation and tortuosity of retinal vessels and formation of multiple aneurysms, with different degrees of leakage and exudates emanating from the blood vessels. | 0 | 2.21 | 1 | 0 |
Hyperthyroid [description not available] | 0 | 12.26 | 40 | 0 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 12.26 | 40 | 0 |
Chloasma [description not available] | 0 | 6.75 | 14 | 1 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 6.75 | 14 | 1 |
Experimental Neoplasms [description not available] | 0 | 7.14 | 41 | 0 |
Post-Traumatic Subarachnoid Hemorrhage [description not available] | 0 | 2.25 | 1 | 0 |
Hematoma, Subdural, Cranial [description not available] | 0 | 2.25 | 1 | 0 |
Brain Contusion A bruise of the brain from an impact of the skull. | 0 | 2.25 | 1 | 0 |
Cranial Epidural Hematoma [description not available] | 0 | 2.25 | 1 | 0 |
Brain Hemorrhage, Cerebral, Traumatic [description not available] | 0 | 2.25 | 1 | 0 |
Hematoma, Subdural, Intracranial Accumulation of blood in the SUBDURAL SPACE over the CEREBRAL HEMISPHERE. | 0 | 2.25 | 1 | 0 |
Cancer of the Thyroid [description not available] | 0 | 4.29 | 7 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 4.29 | 7 | 0 |
Chlamydiaceae Infections Infections with bacteria of the family CHLAMYDIACEAE. | 0 | 2.21 | 1 | 0 |
Ambulation Disorders, Neurologic [description not available] | 0 | 3.2 | 5 | 0 |
Diseases, Metabolic [description not available] | 0 | 5.91 | 14 | 0 |
Metabolic Diseases Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) | 0 | 5.91 | 14 | 0 |
Peste-des-Petits-Ruminants A highly fatal contagious disease of goats and sheep caused by PESTE-DES-PETITS-RUMINANTS VIRUS. The disease may be acute or subacute and is characterized by stomatitis, conjunctivitis, diarrhea, and pneumonia. | 0 | 3.32 | 6 | 0 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 6.74 | 21 | 1 |
Hay Fever [description not available] | 0 | 12.18 | 24 | 8 |
Rhinitis, Allergic, Seasonal Allergic rhinitis that occurs at the same time every year. It is characterized by acute CONJUNCTIVITIS with lacrimation and ITCHING, and regarded as an allergic condition triggered by specific ALLERGENS. | 0 | 12.18 | 24 | 8 |
Aneurysm, Arteriovenous [description not available] | 0 | 7.5 | 50 | 1 |
Infections, Respiratory [description not available] | 0 | 4.84 | 13 | 0 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 4.84 | 13 | 0 |
Adenocystic Carcinoma [description not available] | 0 | 3.08 | 5 | 0 |
Carcinoma, Adenoid Cystic Carcinoma characterized by bands or cylinders of hyalinized or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. When the cylinders occur within masses of epithelial cells, they give the tissue a perforated, sievelike, or cribriform appearance. Such tumors occur in the mammary glands, the mucous glands of the upper and lower respiratory tract, and the salivary glands. They are malignant but slow-growing, and tend to spread locally via the nerves. (Dorland, 27th ed) | 0 | 3.08 | 5 | 0 |
Aspergillus Infection [description not available] | 0 | 7.47 | 21 | 1 |
Dermatomycoses Superficial infections of the skin or its appendages by any of various fungi. | 0 | 3.79 | 4 | 0 |
Nail Fungus [description not available] | 0 | 3.01 | 1 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 7.47 | 21 | 1 |
Onychomycosis A fungal infection of the nail, usually caused by DERMATOPHYTES; YEASTS; or nondermatophyte MOLDS. | 0 | 3.01 | 1 | 0 |
Brain Diseases, Metabolic, Familial [description not available] | 0 | 2.08 | 1 | 0 |
Hemisensory Neglect [description not available] | 0 | 3.79 | 11 | 0 |
Perceptual Disorders Cognitive disorders characterized by an impaired ability to perceive the nature of objects or concepts through use of the sense organs. These include spatial neglect syndromes, where an individual does not attend to visual, auditory, or sensory stimuli presented from one side of the body. | 0 | 3.79 | 11 | 0 |
Callous-Unemotional Traits [description not available] | 0 | 7.37 | 2 | 0 |
Conduct Disorder A repetitive and persistent pattern of behavior in which the basic rights of others or major age-appropriate societal norms or rules are violated. These behaviors include aggressive conduct that causes or threatens physical harm to other people or animals, nonaggressive conduct that causes property loss or damage, deceitfulness or theft, and serious violations of rules. The onset is before age 18. (From DSM-IV, 1994) | 0 | 2.37 | 2 | 0 |
Nevi, Melanocytic [description not available] | 0 | 5.07 | 17 | 0 |
Icterus Gravis Neonatorum [description not available] | 0 | 5.3 | 7 | 0 |
Jaundice, Neonatal Yellow discoloration of the SKIN; MUCOUS MEMBRANE; and SCLERA in the NEWBORN. It is a sign of NEONATAL HYPERBILIRUBINEMIA. Most cases are transient self-limiting (PHYSIOLOGICAL NEONATAL JAUNDICE) occurring in the first week of life, but some can be a sign of pathological disorders, particularly LIVER DISEASES. | 0 | 5.3 | 7 | 0 |
Nevus, Pigmented A nevus containing melanin. The term is usually restricted to nevocytic nevi (round or oval collections of melanin-containing nevus cells occurring at the dermoepidermal junction of the skin or in the dermis proper) or moles, but may be applied to other pigmented nevi. | 0 | 5.07 | 17 | 0 |
Infections, Nematode [description not available] | 0 | 5.51 | 27 | 0 |
Acute Radiation Syndrome A condition caused by a brief whole body exposure to more than one sievert dose equivalent of radiation. Acute radiation syndrome is initially characterized by ANOREXIA; NAUSEA; VOMITING; but can progress to hematological, gastrointestinal, neurological, pulmonary, and other major organ dysfunction. | 0 | 2.08 | 1 | 0 |
Bacillus anthracis Infection [description not available] | 0 | 2.92 | 4 | 0 |
Bacterial Skin Diseases [description not available] | 0 | 3.9 | 4 | 0 |
Anthrax An acute infection caused by the spore-forming bacteria BACILLUS ANTHRACIS. It commonly affects hoofed animals such as sheep and goats. Infection in humans often involves the skin (cutaneous anthrax), the lungs (inhalation anthrax), or the gastrointestinal tract. Anthrax is not contagious and can be treated with antibiotics. | 0 | 2.92 | 4 | 0 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 3.9 | 4 | 0 |
BOF Syndrome [description not available] | 0 | 2.77 | 3 | 0 |
Arteriosclerosis, Coronary [description not available] | 0 | 2.08 | 1 | 0 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 2.08 | 1 | 0 |
Cyclitis, Heterochromic [description not available] | 0 | 6.1 | 31 | 0 |
Iridocyclitis Acute or chronic inflammation of the iris and ciliary body characterized by exudates into the anterior chamber, discoloration of the iris, and constricted, sluggish pupil. Symptoms include radiating pain, photophobia, lacrimation, and interference with vision. | 0 | 6.1 | 31 | 0 |
Neoplasms, Skull [description not available] | 0 | 3.21 | 6 | 0 |
Hypodermyiasis Infestation with larvae of the genus Hypoderma, the warble fly. | 0 | 2.41 | 2 | 0 |
Amyloid Deposits [description not available] | 0 | 2.44 | 2 | 0 |
Loa loa Filariasis [description not available] | 0 | 4.15 | 6 | 0 |
Loiasis A parasitic infection caused by the nematode Loa loa. The vector in the transmission of this infection is the horsefly (Tabanus) or the deerfly or mango fly (Chrysops). The larvae may be seen just beneath the skin or passing through the conjunctiva. Eye lesions are not uncommon. The disease is generally mild and painless. | 0 | 4.15 | 6 | 0 |
Ecchymosis Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia. | 0 | 3.4 | 7 | 0 |
Anton Syndrome [description not available] | 0 | 4.13 | 3 | 0 |
Corneal Edema An excessive amount of fluid in the cornea due to damage of the epithelium or endothelium causing decreased visual acuity. | 0 | 6.26 | 13 | 3 |
Dyskinesia Syndromes [description not available] | 0 | 5.55 | 17 | 0 |
Movement Disorders Syndromes which feature DYSKINESIAS as a cardinal manifestation of the disease process. Included in this category are degenerative, hereditary, post-infectious, medication-induced, post-inflammatory, and post-traumatic conditions. | 0 | 5.55 | 17 | 0 |
Insulin Sensitivity [description not available] | 0 | 2.78 | 3 | 0 |
Insulin Resistance Diminished effectiveness of INSULIN in lowering blood sugar levels: requiring the use of 200 units or more of insulin per day to prevent HYPERGLYCEMIA or KETOSIS. | 0 | 7.78 | 3 | 0 |
Sore Throat [description not available] | 0 | 2.36 | 2 | 0 |
Pharyngitis Inflammation of the throat (PHARYNX). | 0 | 2.36 | 2 | 0 |
Necrobiosis Lipoidica Diabeticorum [description not available] | 0 | 2.08 | 1 | 0 |
Necrobiotic Xanthogranuloma A cutaneous necrobiotic disorder characterized by firm, yellow plaques or nodules, often in a periorbital distribution. It is often accompanied by an elevated ERYTHROCYTE SEDIMENTATION RATE; LEUKOPENIA; and MONOCLONAL GAMMOPATHY (IgG-kappa type) and systemic involvement. | 0 | 2.08 | 1 | 0 |
Necrobiosis Lipoidica A degenerative disease of the dermal connective tissue characterized by the development of erythematous papules or nodules in the pretibial area. The papules form plaques covered with telangiectatic vessels. More than half of the affected patients have diabetes. | 0 | 2.08 | 1 | 0 |
Aseptic Meningitis [description not available] | 0 | 3.32 | 2 | 0 |
Meningitis, Aseptic A syndrome characterized by headache, neck stiffness, low grade fever, and CSF lymphocytic pleocytosis in the absence of an acute bacterial pathogen. Viral meningitis is the most frequent cause although MYCOPLASMA INFECTIONS; RICKETTSIA INFECTIONS; diagnostic or therapeutic procedures; NEOPLASTIC PROCESSES; septic perimeningeal foci; and other conditions may result in this syndrome. (From Adams et al., Principles of Neurology, 6th ed, p745) | 0 | 3.32 | 2 | 0 |
Blood Loss, Postoperative [description not available] | 0 | 2.37 | 2 | 0 |
Infections, Plasmodium [description not available] | 0 | 6.12 | 12 | 0 |
Malaria A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia. | 0 | 6.12 | 12 | 0 |
Infections, Listeria [description not available] | 0 | 3.35 | 7 | 0 |
Dermatitis, Contact, Photoallergic [description not available] | 0 | 7.77 | 19 | 0 |
Iritis Inflammation of the iris characterized by circumcorneal injection, aqueous flare, keratotic precipitates, and constricted and sluggish pupil along with discoloration of the iris. | 0 | 12.58 | 55 | 0 |
Agenesis of Corpus Callosum with Chorioretinal Abnormality [description not available] | 0 | 2.48 | 2 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 4.15 | 17 | 0 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 9.15 | 17 | 0 |
Agenesis of Hemidiaphragm [description not available] | 0 | 2.1 | 1 | 0 |
Kidney Tubular Transport, Inborn Error [description not available] | 0 | 2.67 | 3 | 0 |
Collagen Diseases Historically, a heterogeneous group of acute and chronic diseases, including rheumatoid arthritis, systemic lupus erythematosus, progressive systemic sclerosis, dermatomyositis, etc. This classification was based on the notion that collagen was equivalent to connective tissue, but with the present recognition of the different types of collagen and the aggregates derived from them as distinct entities, the term collagen diseases now pertains exclusively to those inherited conditions in which the primary defect is at the gene level and affects collagen biosynthesis, post-translational modification, or extracellular processing directly. (From Cecil Textbook of Medicine, 19th ed, p1494) | 0 | 10.93 | 26 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 5.06 | 10 | 1 |
Hernias, Diaphragmatic, Congenital Protrusion of abdominal structures into the THORAX as a result of embryologic defects in the DIAPHRAGM often present in the neonatal period. It can be isolated, syndromic, non-syndromic or be a part of chromosome abnormality. Associated pulmonary hypoplasia and PULMONARY HYPERTENSION can further complicate stabilization and surgical intervention. | 0 | 2.1 | 1 | 0 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 3.99 | 5 | 0 |
Emphysema, Mediastinal [description not available] | 0 | 2.08 | 1 | 0 |
Pneumothorax An accumulation of air or gas in the PLEURAL CAVITY, which may occur spontaneously or as a result of trauma or a pathological process. The gas may also be introduced deliberately during PNEUMOTHORAX, ARTIFICIAL. | 0 | 3.99 | 5 | 0 |
Atheroma [description not available] | 0 | 2.1 | 1 | 0 |
Pterygium An abnormal triangular fold of membrane in the interpalpebral fissure, extending from the conjunctiva to the cornea, being immovably united to the cornea at its apex, firmly attached to the sclera throughout its middle portion, and merged with the conjunctiva at its base. (Dorland, 27th ed) | 0 | 10.67 | 29 | 3 |
DDPAC [description not available] | 0 | 3.35 | 6 | 0 |
Frontotemporal Dementia The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight. | 0 | 3.35 | 6 | 0 |
Aging, Premature Changes in the organism associated with senescence, occurring at an accelerated rate. | 0 | 3.01 | 1 | 0 |
Nausea An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses. | 0 | 11.97 | 11 | 3 |
Altidudinal Hemianopia [description not available] | 0 | 4.34 | 21 | 0 |
Bowen Disease [description not available] | 0 | 2.36 | 2 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 3.32 | 7 | 0 |
Craniopharyngioma A benign pituitary-region neoplasm that originates from Rathke's pouch. The two major histologic and clinical subtypes are adamantinous (or classical) craniopharyngioma and papillary craniopharyngioma. The adamantinous form presents in children and adolescents as an expanding cystic lesion in the pituitary region. The cystic cavity is filled with a black viscous substance and histologically the tumor is composed of adamantinomatous epithelium and areas of calcification and necrosis. Papillary craniopharyngiomas occur in adults, and histologically feature a squamous epithelium with papillations. (From Joynt, Clinical Neurology, 1998, Ch14, p50) | 0 | 3.32 | 7 | 0 |
Dermatitis, Irritant A non-allergic contact dermatitis caused by prolonged exposure to irritants and not explained by delayed hypersensitivity mechanisms. | 0 | 4.65 | 6 | 0 |
Central Nervous System Helminthiasis Infections of the BRAIN; SPINAL CORD; or MENINGES caused by HELMINTHS (parasitic worms). | 0 | 2.76 | 3 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 10.65 | 60 | 0 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 9.04 | 72 | 0 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 2.67 | 3 | 0 |
Mandibular Retroposition [description not available] | 0 | 2.1 | 1 | 0 |
Angle Class III [description not available] | 0 | 3.12 | 5 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 5.75 | 5 | 0 |
Pulmonary Fibrosis A process in which normal lung tissues are progressively replaced by FIBROBLASTS and COLLAGEN causing an irreversible loss of the ability to transfer oxygen into the bloodstream via PULMONARY ALVEOLI. Patients show progressive DYSPNEA finally resulting in death. | 0 | 5.75 | 5 | 0 |
Cancer of Colon [description not available] | 0 | 3.09 | 5 | 0 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 3.09 | 5 | 0 |
Dysentery, Shiga bacillus [description not available] | 0 | 4.14 | 6 | 0 |
Dysentery, Bacillary DYSENTERY caused by gram-negative rod-shaped enteric bacteria (ENTEROBACTERIACEAE), most often by the genus SHIGELLA. Shigella dysentery, Shigellosis, is classified into subgroups according to syndrome severity and the infectious species. Group A: SHIGELLA DYSENTERIAE (severest); Group B: SHIGELLA FLEXNERI; Group C: SHIGELLA BOYDII; and Group D: SHIGELLA SONNEI (mildest). | 0 | 4.14 | 6 | 0 |
Ataxia Telangiectasia Syndrome [description not available] | 0 | 3.36 | 7 | 0 |
Ataxia Telangiectasia An autosomal recessive inherited disorder characterized by choreoathetosis beginning in childhood, progressive CEREBELLAR ATAXIA; TELANGIECTASIS of CONJUNCTIVA and SKIN; DYSARTHRIA; B- and T-cell immunodeficiency, and RADIOSENSITIVITY to IONIZING RADIATION. Affected individuals are prone to recurrent sinobronchopulmonary infections, lymphoreticular neoplasms, and other malignancies. Serum ALPHA-FETOPROTEINS are usually elevated. (Menkes, Textbook of Child Neurology, 5th ed, p688) The gene for this disorder (ATM) encodes a cell cycle checkpoint protein kinase and has been mapped to chromosome 11 (11q22-q23). | 0 | 8.36 | 7 | 0 |
Aneurysm, Ruptured The tearing or bursting of the weakened wall of the aneurysmal sac, usually heralded by sudden worsening pain. The great danger of a ruptured aneurysm is the large amount of blood spilling into the surrounding tissues and cavities, causing HEMORRHAGIC SHOCK. | 0 | 3.39 | 2 | 0 |
Hemorrhage, Subarachnoid [description not available] | 0 | 5.26 | 21 | 0 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 10.26 | 21 | 0 |
Autosomal Dominant Juvenile Parkinson Disease [description not available] | 0 | 3.6 | 9 | 0 |
Parkinsonian Disorders A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA. | 0 | 3.6 | 9 | 0 |
Hemorrhagic Fever, Epidemic [description not available] | 0 | 2.67 | 3 | 0 |
Hemorrhagic Fever with Renal Syndrome An acute febrile disease occurring predominately in Asia. It is characterized by fever, prostration, vomiting, hemorrhagic phenonema, shock, and renal failure. It is caused by any one of several closely related species of the genus Hantavirus. The most severe form is caused by HANTAAN VIRUS whose natural host is the rodent Apodemus agrarius. Milder forms are caused by SEOUL VIRUS and transmitted by the rodents Rattus rattus and R. norvegicus, and the PUUMALA VIRUS with transmission by Clethrionomys galreolus. | 0 | 2.67 | 3 | 0 |
Flavivirus Infections Infections with viruses of the genus FLAVIVIRUS, family FLAVIVIRIDAE. | 0 | 2.1 | 1 | 0 |
Food Poisoning [description not available] | 0 | 3.83 | 4 | 0 |
Fasciola Infection [description not available] | 0 | 3.63 | 3 | 0 |
Fascioliasis Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA. | 0 | 3.63 | 3 | 0 |
Neurilemoma [description not available] | 0 | 3.2 | 6 | 0 |
Neoplasms, Nerve Sheath [description not available] | 0 | 2.52 | 2 | 0 |
Neurilemmoma A neoplasm that arises from SCHWANN CELLS of the cranial, peripheral, and autonomic nerves. Clinically, these tumors may present as a cranial neuropathy, abdominal or soft tissue mass, intracranial lesion, or with spinal cord compression. Histologically, these tumors are encapsulated, highly vascular, and composed of a homogenous pattern of biphasic fusiform-shaped cells that may have a palisaded appearance. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp964-5) | 0 | 3.2 | 6 | 0 |
Nerve Sheath Neoplasms Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category. | 0 | 2.52 | 2 | 0 |
Locomotor Ataxia [description not available] | 0 | 3.94 | 5 | 0 |
Night Blindness Failure or imperfection of vision at night or in dim light, with good vision only on bright days. (Dorland, 27th ed) | 0 | 4.42 | 23 | 0 |
Anaphylactic Reaction [description not available] | 0 | 6.61 | 38 | 0 |
Anaphylaxis An acute hypersensitivity reaction due to exposure to a previously encountered ANTIGEN. The reaction may include rapidly progressing URTICARIA, respiratory distress, vascular collapse, systemic SHOCK, and death. | 0 | 6.61 | 38 | 0 |
Bone Diseases Diseases of BONES. | 0 | 4.02 | 15 | 0 |
Angioid Streaks Small breaks in the elastin-filled tissue of the retina. | 0 | 3.88 | 13 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 5.8 | 37 | 0 |
Aneurysm Pathological outpouching or sac-like dilatation in the wall of any blood vessel (ARTERIES or VEINS) or the heart (HEART ANEURYSM). It indicates a thin and weakened area in the wall which may later rupture. Aneurysms are classified by location, etiology, or other characteristics. | 0 | 5.8 | 37 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 4.93 | 15 | 0 |
Heat Collapse [description not available] | 0 | 2.34 | 2 | 0 |
Disseminated Fusariosis [description not available] | 0 | 2.1 | 1 | 0 |
Fusariosis OPPORTUNISTIC INFECTIONS with the soil fungus FUSARIUM. Typically the infection is limited to the nail plate (ONYCHOMYCOSIS). The infection can however become systemic especially in an IMMUNOCOMPROMISED HOST (e.g., NEUTROPENIA) and results in cutaneous and subcutaneous lesions, fever, KERATITIS, and pulmonary infections. | 0 | 2.1 | 1 | 0 |
Air Embolism [description not available] | 0 | 8.07 | 5 | 0 |
Cranial Airocele [description not available] | 0 | 2.1 | 1 | 0 |
Pervasive Child Development Disorders [description not available] | 0 | 5.08 | 9 | 1 |
Child Development Disorders, Pervasive Severe distortions in the development of many basic psychological functions that are not normal for any stage in development. These distortions are manifested in sustained social impairment, speech abnormalities, and peculiar motor movements. | 0 | 5.08 | 9 | 1 |
Autosomal Chromosome Disorders [description not available] | 0 | 6.8 | 29 | 0 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 4.35 | 20 | 0 |
Chromosomal Instability An increased tendency to acquire CHROMOSOME ABERRATIONS when various processes involved in chromosome replication, repair, or segregation are dysfunctional. | 0 | 2.45 | 2 | 0 |
Cardiac Cancer [description not available] | 0 | 2.1 | 1 | 0 |
Angiomyxoma [description not available] | 0 | 2.43 | 2 | 0 |
Primary Hyperparathyroidism [description not available] | 0 | 2.52 | 2 | 0 |
Adenoma, Basal Cell [description not available] | 0 | 4.03 | 15 | 0 |
Icterus [description not available] | 0 | 3.05 | 5 | 0 |
Cancer of Parathyroid [description not available] | 0 | 2.1 | 1 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 4.03 | 15 | 0 |
Jaundice A clinical manifestation of HYPERBILIRUBINEMIA, characterized by the yellowish staining of the SKIN; MUCOUS MEMBRANE; and SCLERA. Clinical jaundice usually is a sign of LIVER dysfunction. | 0 | 3.05 | 5 | 0 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 2.1 | 1 | 0 |
Hyperparathyroidism, Primary A condition of abnormally elevated output of PARATHYROID HORMONE due to parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. It is characterized by the combination of HYPERCALCEMIA, phosphaturia, elevated renal 1,25-DIHYDROXYVITAMIN D3 synthesis, and increased BONE RESORPTION. | 0 | 2.52 | 2 | 0 |
Infections, Poxviridae [description not available] | 0 | 4.06 | 5 | 0 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 2.52 | 2 | 0 |
Cancer of Maxillary Sinus [description not available] | 0 | 3.07 | 5 | 0 |
Squamous Cell Carcinoma of Head and Neck The most common type of head and neck carcinoma that originates from cells on the surface of the NASAL CAVITY; MOUTH; PARANASAL SINUSES, SALIVARY GLANDS, and LARYNX. Mutations in TNFRSF10B, PTEN, and ING1 genes are associated with this cancer. | 0 | 2.52 | 2 | 0 |
Cell Transformation, Neoplastic Cell changes manifested by escape from control mechanisms, increased growth potential, alterations in the cell surface, karyotypic abnormalities, morphological and biochemical deviations from the norm, and other attributes conferring the ability to invade, metastasize, and kill. | 0 | 5.57 | 17 | 0 |
Hypergonadotropic Hypogonadism [description not available] | 0 | 2.75 | 3 | 0 |
Hypogonadism Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism). | 0 | 2.75 | 3 | 0 |
Ethmoid Sinusitis Inflammation of the NASAL MUCOSA in the ETHMOID SINUS. It may present itself as an acute (infectious) or chronic (allergic) condition. | 0 | 2.87 | 4 | 0 |
Porphyria Cutanea Tarda An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form. | 0 | 2.42 | 2 | 0 |
Chicken Pox [description not available] | 0 | 4.94 | 15 | 0 |
Chickenpox A highly contagious infectious disease caused by the varicella-zoster virus (HERPESVIRUS 3, HUMAN). It usually affects children, is spread by direct contact or respiratory route via droplet nuclei, and is characterized by the appearance on the skin and mucous membranes of successive crops of typical pruritic vesicular lesions that are easily broken and become scabbed. Chickenpox is relatively benign in children, but may be complicated by pneumonia and encephalitis in adults. (From Dorland, 27th ed) | 0 | 4.94 | 15 | 0 |
Abnormal Deep Tendon Reflex [description not available] | 0 | 6.57 | 7 | 1 |
Reflex, Abnormal An abnormal response to a stimulus applied to the sensory components of the nervous system. This may take the form of increased, decreased, or absent reflexes. | 0 | 6.57 | 7 | 1 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 5.29 | 13 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 3.01 | 1 | 0 |
Cancer of Cervix [description not available] | 0 | 2.1 | 1 | 0 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 2.1 | 1 | 0 |
Asthenopia Term generally used to describe complaints related to refractive error, ocular muscle imbalance, including pain or aching around the eyes, burning and itchiness of the eyelids, ocular fatigue, and headaches. | 0 | 5.72 | 21 | 1 |
Combined Immunodeficiency, X-Linked [description not available] | 0 | 2.1 | 1 | 0 |
X-Linked Combined Immunodeficiency Diseases Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified. | 0 | 2.1 | 1 | 0 |
Sexually Transmitted Diseases Diseases due to or propagated by sexual contact. | 0 | 4.75 | 7 | 1 |
Lymphogranuloma Inguinale [description not available] | 0 | 2.86 | 4 | 0 |
Angioneurotic Edema [description not available] | 0 | 3.34 | 7 | 0 |
Angioedema Swelling involving the deep DERMIS, subcutaneous, or submucosal tissues, representing localized EDEMA. Angioedema often occurs in the face, lips, tongue, and larynx. | 0 | 3.34 | 7 | 0 |
Nevus of Ota A macular lesion on the side of the FACE, involving the CONJUNCTIVA and EYELIDS, as well as the adjacent facial skin, SCLERA; OCULOMOTOR MUSCLES; and PERIOSTEUM. Histological features vary from those of a MONGOLIAN SPOT to those of a BLUE NEVUS. | 0 | 4 | 5 | 0 |
Multiple Primary Neoplasms [description not available] | 0 | 5.98 | 10 | 1 |
E coli Infections [description not available] | 0 | 3.2 | 6 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 3.2 | 6 | 0 |
Behavior Disorder, Rapid Eye Movement Sleep [description not available] | 0 | 2.1 | 1 | 0 |
Excessive Periodic Sleep-Related Leg Movements [description not available] | 0 | 2.1 | 1 | 0 |
REM Sleep Behavior Disorder A disorder characterized by episodes of vigorous and often violent motor activity during REM sleep (SLEEP, REM). The affected individual may inflict self injury or harm others, and is difficult to awaken from this condition. Episodes are usually followed by a vivid recollection of a dream that is consistent with the aggressive behavior. This condition primarily affects adult males. (From Adams et al., Principles of Neurology, 6th ed, p393) | 0 | 2.1 | 1 | 0 |
Hemothorax Hemorrhage within the pleural cavity. | 0 | 3.01 | 1 | 0 |
Ectopic Pregnancy [description not available] | 0 | 3.56 | 3 | 0 |
Edema, Pulmonary [description not available] | 0 | 3.99 | 5 | 0 |
Pleural Effusion Presence of fluid in the pleural cavity resulting from excessive transudation or exudation from the pleural surfaces. It is a sign of disease and not a diagnosis in itself. | 0 | 3.01 | 1 | 0 |
Pregnancy, Ectopic A potentially life-threatening condition in which EMBRYO IMPLANTATION occurs outside the cavity of the UTERUS. Most ectopic pregnancies ( | 0 | 3.56 | 3 | 0 |
Pulmonary Edema Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE in the PULMONARY ALVEOLI, and can be life-threatening. | 0 | 3.99 | 5 | 0 |
Convulsive Generalized Seizure Disorder [description not available] | 0 | 2.1 | 1 | 0 |
Erythremia [description not available] | 0 | 3.04 | 5 | 0 |
Hemorrhagic Thrombocythemia [description not available] | 0 | 2.11 | 1 | 0 |
Erythermalgia [description not available] | 0 | 2.11 | 1 | 0 |
Erythromelalgia A peripheral arterial disease that is characterized by the triad of ERYTHEMA, burning PAIN, and increased SKIN TEMPERATURE of the extremities (or red, painful extremities). Erythromelalgia may be classified as primary or idiopathic, familial or non-familial. Secondary erythromelalgia is associated with other diseases, the most common being MYELOPROLIFERATIVE DISORDERS. | 0 | 2.11 | 1 | 0 |
Polycythemia Vera A myeloproliferative disorder of unknown etiology, characterized by abnormal proliferation of all hematopoietic bone marrow elements and an absolute increase in red cell mass and total blood volume, associated frequently with splenomegaly, leukocytosis, and thrombocythemia. Hematopoiesis is also reactive in extramedullary sites (liver and spleen). In time myelofibrosis occurs. | 0 | 3.04 | 5 | 0 |
Thrombocythemia, Essential A clinical syndrome characterized by repeated spontaneous hemorrhages and a remarkable increase in the number of circulating platelets. | 0 | 2.11 | 1 | 0 |
Lens Diseases Diseases involving the CRYSTALLINE LENS. | 0 | 5.76 | 15 | 0 |
Gardner Syndrome A variant of ADENOMATOUS POLYPOSIS COLI caused by mutation in the APC gene (GENES, APC) on CHROMOSOME 5. It is characterized by not only the presence of multiple colonic polyposis but also extracolonic ADENOMATOUS POLYPS in the UPPER GASTROINTESTINAL TRACT; the EYE; the SKIN; the SKULL; and the FACIAL BONES; as well as malignancy in organs other than the GI tract. | 0 | 2.41 | 2 | 0 |
Osteoma A benign tumor composed of bone tissue or a hard tumor of bonelike structure developing on a bone (homoplastic osteoma) or on other structures (heteroplastic osteoma). (From Dorland, 27th ed) | 0 | 8.2 | 6 | 0 |
Teeth, Unerupted [description not available] | 0 | 2.1 | 1 | 0 |
Lens Dislocation [description not available] | 0 | 4.28 | 19 | 0 |
Eaton-Lambert Myasthenic Syndrome [description not available] | 0 | 2.41 | 2 | 0 |
Lambert-Eaton Myasthenic Syndrome An autoimmune disease characterized by weakness and fatigability of proximal muscles, particularly of the pelvic girdle, lower extremities, trunk, and shoulder girdle. There is relative sparing of extraocular and bulbar muscles. CARCINOMA, SMALL CELL of the lung is a frequently associated condition, although other malignancies and autoimmune diseases may be associated. Muscular weakness results from impaired impulse transmission at the NEUROMUSCULAR JUNCTION. Presynaptic calcium channel dysfunction leads to a reduced amount of acetylcholine being released in response to stimulation of the nerve. (From Adams et al., Principles of Neurology, 6th ed, pp 1471) | 0 | 2.41 | 2 | 0 |
Nasal Diseases [description not available] | 0 | 3.75 | 11 | 0 |
Cystic Kidney Diseases [description not available] | 0 | 2.11 | 1 | 0 |
Hereditary Optic Atrophy [description not available] | 0 | 3.19 | 6 | 0 |
Kidney Diseases, Cystic A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC). | 0 | 2.11 | 1 | 0 |
Nociceptive Pain Dull or sharp aching pain caused by stimulated NOCICEPTORS due to tissue injury, inflammation or diseases. It can be divided into somatic or tissue pain and VISCERAL PAIN. | 0 | 2.52 | 2 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 8.73 | 42 | 1 |
Prodromal Characteristics [description not available] | 0 | 2.11 | 1 | 0 |
Antisocial Behavior Behavior that sharply deviates from social norms and violates rights of others | 0 | 2.81 | 3 | 0 |
Aneurysm, Aortic [description not available] | 0 | 2.11 | 1 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 2.11 | 1 | 0 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 2.71 | 3 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 7.67 | 3 | 0 |
Lung Diseases, Interstitial A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of PULMONARY ALVEOLI that extends to the interstitium and beyond leading to diffuse PULMONARY FIBROSIS. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features. | 0 | 2.71 | 3 | 0 |
Grippe [description not available] | 0 | 3.91 | 13 | 0 |
Influenza, Human An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia. | 0 | 3.91 | 13 | 0 |
Uremia A clinical syndrome associated with the retention of renal waste products or uremic toxins in the blood. It is usually the result of RENAL INSUFFICIENCY. Most uremic toxins are end products of protein or nitrogen CATABOLISM, such as UREA or CREATININE. Severe uremia can lead to multiple organ dysfunctions with a constellation of symptoms. | 0 | 9.59 | 6 | 0 |
Asthenia Clinical sign or symptom manifested as debility, or lack or loss of strength and energy. | 0 | 2.36 | 2 | 0 |
Cavernous Sinus Thrombophlebitis [description not available] | 0 | 5 | 9 | 0 |
MODS [description not available] | 0 | 4.3 | 2 | 0 |
Multiple Organ Failure A progressive condition usually characterized by combined failure of several organs such as the lungs, liver, kidney, along with some clotting mechanisms, usually postinjury or postoperative. | 0 | 4.3 | 2 | 0 |
Aspiration, Respiratory [description not available] | 0 | 2.1 | 1 | 0 |
Infections, Mononegavirales [description not available] | 0 | 2.1 | 1 | 0 |
Complications, Parasitic Pregnancy [description not available] | 0 | 5.44 | 5 | 0 |
Dermal Hypoplasia, Focal [description not available] | 0 | 2.42 | 2 | 0 |
Appetite Disorders [description not available] | 0 | 2.1 | 1 | 0 |
Feeding and Eating Disorders A group of disorders characterized by physiological and psychological disturbances in appetite or food intake. | 0 | 2.1 | 1 | 0 |
Urinary Retention Inability to empty the URINARY BLADDER with voiding (URINATION). | 0 | 2.1 | 1 | 0 |
Birth Injuries Mechanical or anoxic trauma incurred by the infant during labor or delivery. | 0 | 2.88 | 4 | 0 |
Precordial Catch [description not available] | 0 | 2.42 | 2 | 0 |
Multiple Pulmonary Nodules A number of small lung lesions characterized by small round masses of 2- to 3-mm in diameter. They are usually detected by chest CT scans (COMPUTED TOMOGRAPHY, X-RAY). Such nodules can be associated with metastases of malignancies inside or outside the lung, benign granulomas, or other lesions. | 0 | 3.42 | 2 | 0 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 2.42 | 2 | 0 |
Lupus Erythematosus Panniculitis [description not available] | 0 | 2.11 | 1 | 0 |
Neoplasm Regression, Spontaneous Disappearance of a neoplasm or neoplastic state without the intervention of therapy. | 0 | 3.06 | 5 | 0 |
Phantom Limb Perception of painful and nonpainful phantom sensations that occur following the complete or partial loss of a limb. The majority of individuals with an amputated extremity will experience the impression that the limb is still present, and in many cases, painful. (From Neurol Clin 1998 Nov;16(4):919-36; Brain 1998 Sep;121(Pt 9):1603-30) | 0 | 3.3 | 2 | 0 |
Aphakia, Postcataract Absence of the crystalline lens resulting from cataract extraction. | 0 | 9.18 | 48 | 1 |
Child Behavior Disorders Disturbances considered to be pathological based on age and stage appropriateness, e.g., conduct disturbances and anaclitic depression. This concept does not include psychoneuroses, psychoses, or personality disorders with fixed patterns. | 0 | 2.65 | 3 | 0 |
Acquired Communication Disorders [description not available] | 0 | 2.11 | 1 | 0 |
Communication Disorders Disorders of verbal and nonverbal communication caused by receptive or expressive LANGUAGE DISORDERS, cognitive dysfunction (e.g., MENTAL RETARDATION), psychiatric conditions, and HEARING DISORDERS. | 0 | 2.11 | 1 | 0 |
Inferior Dislocation [description not available] | 0 | 3.66 | 10 | 0 |
Dehiscence, Surgical Wound [description not available] | 0 | 3.09 | 5 | 0 |
Zygomatic Fractures Fractures of the zygoma. | 0 | 4.88 | 8 | 1 |
Anterior Cerebral Circulation Infarction [description not available] | 0 | 2.97 | 4 | 0 |
Aldosteronism [description not available] | 0 | 2.11 | 1 | 0 |
Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. | 0 | 2.11 | 1 | 0 |
Brain Infarction Tissue NECROSIS in any area of the brain, including the CEREBRAL HEMISPHERES, the CEREBELLUM, and the BRAIN STEM. Brain infarction is the result of a cascade of events initiated by inadequate blood flow through the brain that is followed by HYPOXIA and HYPOGLYCEMIA in brain tissue. Damage may be temporary, permanent, selective or pan-necrosis. | 0 | 2.97 | 4 | 0 |
Cancer of Duodenum [description not available] | 0 | 2.11 | 1 | 0 |
Retinal Dysplasia Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary. | 0 | 3.11 | 5 | 0 |
Dermatitis, Occupational A recurrent contact dermatitis caused by substances found in the work place. | 0 | 3.35 | 7 | 0 |
Hypotension, Postural [description not available] | 0 | 3.07 | 5 | 0 |
Hypotension, Orthostatic A significant drop in BLOOD PRESSURE after assuming a standing position. Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. Symptoms generally include DIZZINESS, blurred vision, and SYNCOPE. | 0 | 3.07 | 5 | 0 |
Colorectal Cancer [description not available] | 0 | 2.93 | 4 | 0 |
Colorectal Neoplasms Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI. | 0 | 2.93 | 4 | 0 |
Cerebrovascular Moyamoya Disease [description not available] | 0 | 2.45 | 2 | 0 |
Angle Class II [description not available] | 0 | 2.74 | 3 | 0 |
Aganglionic Megacolon [description not available] | 0 | 2.69 | 3 | 0 |
Hirschsprung Disease Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON. | 0 | 7.69 | 3 | 0 |
Cell Transformation, Viral An inheritable change in cells manifested by changes in cell division and growth and alterations in cell surface properties. It is induced by infection with a transforming virus. | 0 | 3.83 | 4 | 0 |
Congenital Mesodermal Dysmorphodystrophy [description not available] | 0 | 2.11 | 1 | 0 |
Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome [description not available] | 0 | 2.48 | 2 | 0 |
Rett Syndrome An inherited neurological developmental disorder that is associated with X-LINKED INHERITANCE and may be lethal in utero to hemizygous males. The affected female is normal until the age of 6-25 months when progressive loss of voluntary control of hand movements and communication skills; ATAXIA; SEIZURES; autistic behavior; intermittent HYPERVENTILATION; and HYPERAMMONEMIA appear. (From Menkes, Textbook of Child Neurology, 5th ed, p199) | 0 | 7.48 | 2 | 0 |
Asperger Disease [description not available] | 0 | 9.61 | 53 | 0 |
Asperger Syndrome A disorder beginning in childhood whose essential features are persistent impairment in reciprocal social communication and social interaction, and restricted, repetitive patterns of behavior, interests, or activities. These symptoms may limit or impair everyday functioning. (From DSM-5) | 0 | 9.61 | 53 | 0 |
Preterm Birth [description not available] | 0 | 5.23 | 7 | 0 |
Premature Birth CHILDBIRTH before 37 weeks of PREGNANCY (259 days from the first day of the mother's last menstrual period, or 245 days after FERTILIZATION). | 0 | 5.23 | 7 | 0 |
Angiolymphoid Hyperplasia with Eosinophilia Solitary or multiple benign cutaneous nodules comprised of immature and mature vascular structures intermingled with endothelial cells and a varied infiltrate of eosinophils, histiocytes, lymphocytes, and mast cells. | 0 | 2.11 | 1 | 0 |
Acrocephalosyndactylia Congenital craniostenosis with syndactyly. | 0 | 3.3 | 6 | 0 |
Varices [description not available] | 0 | 3.23 | 6 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 3.23 | 6 | 0 |
Erysipelas An acute infection of the skin caused by species of STREPTOCOCCUS. This disease most frequently affects infants, young children, and the elderly. Characteristics include pink-to-red lesions that spread rapidly and are warm to the touch. The commonest site of involvement is the face. | 0 | 2.11 | 1 | 0 |
Injuries, Neck [description not available] | 0 | 2.86 | 4 | 0 |
Wounds, Penetrating Wounds caused by objects penetrating the skin. | 0 | 7.18 | 36 | 1 |
Suffocation [description not available] | 0 | 4.26 | 7 | 0 |
Asphyxia A pathological condition caused by lack of oxygen, manifested in impending or actual cessation of life. | 0 | 9.26 | 7 | 0 |
Hematologic Malignancies [description not available] | 0 | 5.11 | 3 | 1 |
Hematologic Neoplasms Neoplasms located in the blood and blood-forming tissue (the bone marrow and lymphatic tissue). The commonest forms are the various types of LEUKEMIA, of LYMPHOMA, and of the progressive, life-threatening forms of the MYELODYSPLASTIC SYNDROMES. | 0 | 5.11 | 3 | 1 |
Consciousness, Loss of [description not available] | 0 | 3.47 | 8 | 0 |
Cafe-au-Lait Spots Light brown pigmented macules associated with NEUROFIBROMATOSIS and Albright's syndrome (see FIBROUS DYSPLASIA, POLYOSTOTIC). | 0 | 3.39 | 2 | 0 |
Anxiety Neuroses [description not available] | 0 | 3.19 | 6 | 0 |
Anankastic Personality [description not available] | 0 | 2.11 | 1 | 0 |
Anxiety Disorders Persistent and disabling ANXIETY. | 0 | 3.19 | 6 | 0 |
Neurofibroma A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016) | 0 | 9.12 | 6 | 0 |
Obsessive-Compulsive Disorder An anxiety disorder characterized by recurrent, persistent obsessions or compulsions. Obsessions are the intrusive ideas, thoughts, or images that are experienced as senseless or repugnant. Compulsions are repetitive and seemingly purposeful behavior which the individual generally recognizes as senseless and from which the individual does not derive pleasure although it may provide a release from tension. | 0 | 2.11 | 1 | 0 |
Acute Onset Aura Migraine [description not available] | 0 | 2.46 | 2 | 0 |
Common Migraine [description not available] | 0 | 2.13 | 1 | 0 |
Migraine with Aura A subtype of migraine disorder, characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred VISION; HALLUCINATIONS; VERTIGO; NUMBNESS; and difficulty in concentrating and speaking. Aura is usually followed by features of the COMMON MIGRAINE, such as PHOTOPHOBIA; PHONOPHOBIA; and NAUSEA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 2.46 | 2 | 0 |
Migraine without Aura Recurrent unilateral pulsatile headaches, not preceded or accompanied by an aura, in attacks lasting 4-72 hours. It is characterized by PAIN of moderate to severe intensity; aggravated by physical activity; and associated with NAUSEA and / or PHOTOPHOBIA and PHONOPHOBIA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 2.13 | 1 | 0 |
Acoustic Neurinoma, Bilateral [description not available] | 0 | 2.13 | 1 | 0 |
Neurofibromatosis 2 An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life. | 0 | 2.13 | 1 | 0 |
Hydronephrosis Abnormal enlargement or swelling of a KIDNEY due to dilation of the KIDNEY CALICES and the KIDNEY PELVIS. It is often associated with obstruction of the URETER or chronic kidney diseases that prevents normal drainage of urine into the URINARY BLADDER. | 0 | 2.11 | 1 | 0 |
Familial Hyperpotassemia and Hypertension [description not available] | 0 | 2.11 | 1 | 0 |
Polyuria Urination of a large volume of urine with an increase in urinary frequency, commonly seen in diabetes (DIABETES MELLITUS; DIABETES INSIPIDUS). | 0 | 2.68 | 3 | 0 |
Pseudohypoaldosteronism A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders characterized by neonatal hypertension, HYPERKALEMIA, increased RENIN activity and ALDOSTERONE concentration. The Type I features HYPERKALEMIA with sodium wasting; Type II, HYPERKALEMIA without sodium wasting. Pseudohypoaldosteronism can be the result of a defective renal electrolyte transport protein or acquired after KIDNEY TRANSPLANTATION. | 0 | 2.11 | 1 | 0 |
Feuerstein-Mims Syndrome [description not available] | 0 | 2.52 | 2 | 0 |
Adenoma, Sweat Gland A benign neoplasm derived from epithelial cells of sweat glands. (Stedman, 25th ed) | 0 | 2.13 | 1 | 0 |
Neoplasms, Sweat Gland [description not available] | 0 | 2.42 | 2 | 0 |
Pulmonary Consumption [description not available] | 0 | 7.35 | 27 | 1 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 7.35 | 27 | 1 |
Pythiosis A granulomatous disease caused by the aquatic organism PYTHIUM insidiosum and occurring primarily in horses, cattle, dogs, cats, fishes, and rarely in humans. It is classified into three forms: ocular, cutaneous, and arterial. | 0 | 2.11 | 1 | 0 |
Pulmonary Sarcoidosis [description not available] | 0 | 2.52 | 2 | 0 |
Sarcoidosis, Pulmonary Sarcoidosis affecting predominantly the lungs, the site most frequently involved and most commonly causing morbidity and mortality in sarcoidosis. Pulmonary sarcoidosis is characterized by sharply circumscribed granulomas in the alveolar, bronchial, and vascular walls, composed of tightly packed cells derived from the mononuclear phagocyte system. The clinical symptoms when present are dyspnea upon exertion, nonproductive cough, and wheezing. (Cecil Textbook of Medicine, 19th ed, p431) | 0 | 2.52 | 2 | 0 |
Pars Planitis Form of granulomatous uveitis occurring in the region of the pars plana. This disorder is a common condition with no detectable focal pathology. It causes fibrovascular proliferation at the inferior ora serrata. | 0 | 3.34 | 2 | 0 |
Brain Vascular Disorders [description not available] | 0 | 9.56 | 49 | 2 |
Cerebrovascular Disorders A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others. | 0 | 9.56 | 49 | 2 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 6.44 | 9 | 2 |
Latent Stage Syphilis [description not available] | 0 | 3.77 | 4 | 0 |
Viremia The presence of viruses in the blood. | 0 | 4.31 | 4 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 2.52 | 2 | 0 |
Cardiac Arrest, Sudden [description not available] | 0 | 2.11 | 1 | 0 |
Cardiomyopathies A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS). | 0 | 2.52 | 2 | 0 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 2.11 | 1 | 0 |
4 Hydroxyphenylpyruvate Dioxygenase Deficiency Disease [description not available] | 0 | 2.11 | 1 | 0 |
Bare Lymphocyte Syndrome [description not available] | 0 | 3.04 | 5 | 0 |
Hypogammaglobulinemia [description not available] | 0 | 2.11 | 1 | 0 |
Agammaglobulinemia An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood. | 0 | 2.11 | 1 | 0 |
Severe Combined Immunodeficiency Group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. It is inherited as an X-linked or autosomal recessive defect. Mutations occurring in many different genes cause human Severe Combined Immunodeficiency (SCID). | 0 | 3.04 | 5 | 0 |
Tyrosinemias A group of disorders which have in common elevations of tyrosine in the blood and urine secondary to an enzyme deficiency. Type I tyrosinemia features episodic weakness, self-mutilation, hepatic necrosis, renal tubular injury, and seizures and is caused by a deficiency of the enzyme fumarylacetoacetase. Type II tyrosinemia features INTELLECTUAL DISABILITY, painful corneal ulcers, and keratoses of the palms and plantar surfaces and is caused by a deficiency of the enzyme TYROSINE TRANSAMINASE. Type III tyrosinemia features INTELLECTUAL DISABILITY and is caused by a deficiency of the enzyme 4-HYDROXYPHENYLPYRUVATE DIOXYGENASE. (Menkes, Textbook of Child Neurology, 5th ed, pp42-3) | 0 | 2.11 | 1 | 0 |
Central Nervous System Disease [description not available] | 0 | 6.73 | 27 | 0 |
Central Nervous System Diseases Diseases of any component of the brain (including the cerebral hemispheres, diencephalon, brain stem, and cerebellum) or the spinal cord. | 0 | 6.73 | 27 | 0 |
Hypomelanosis [description not available] | 0 | 2.97 | 4 | 0 |
Hypopigmentation A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections. | 0 | 2.97 | 4 | 0 |
Genital Herpes [description not available] | 0 | 4.08 | 3 | 1 |
Herpes Genitalis Infection of the genitals (GENITALIA) with HERPES SIMPLEX VIRUS in either the males or the females. | 0 | 4.08 | 3 | 1 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 5.96 | 10 | 1 |
Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325) | 0 | 5.96 | 10 | 1 |
Lysosomal Enzyme Disorders [description not available] | 0 | 3.04 | 1 | 0 |
Toxascariasis Infections with nematodes of the genus TOXASCARIS. | 0 | 3.04 | 1 | 0 |
Adie Pupil [description not available] | 0 | 4.25 | 7 | 0 |
Angiostrongylus Infections [description not available] | 0 | 3.67 | 3 | 0 |
Encephalitis, Viral Inflammation of brain parenchymal tissue as a result of viral infection. Encephalitis may occur as primary or secondary manifestation of TOGAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; BUNYAVIRIDAE INFECTIONS; PICORNAVIRIDAE INFECTIONS; PARAMYXOVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RETROVIRIDAE INFECTIONS; and ARENAVIRIDAE INFECTIONS. | 0 | 4.41 | 8 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 11.74 | 33 | 0 |
Acquired Immunodeficiency Syndrome An acquired defect of cellular immunity associated with infection by the human immunodeficiency virus (HIV), a CD4-positive T-lymphocyte count under 200 cells/microliter or less than 14% of total lymphocytes, and increased susceptibility to opportunistic infections and malignant neoplasms. Clinical manifestations also include emaciation (wasting) and dementia. These elements reflect criteria for AIDS as defined by the CDC in 1993. | 0 | 11.74 | 33 | 0 |
Peripheral Arterial Diseases [description not available] | 0 | 3.04 | 1 | 0 |
Peripheral Arterial Disease Lack of perfusion in the EXTREMITIES resulting from atherosclerosis. It is characterized by INTERMITTENT CLAUDICATION, and an ANKLE BRACHIAL INDEX of 0.9 or less. | 0 | 3.04 | 1 | 0 |
AIDS-Related Opportunistic Infections Opportunistic infections found in patients who test positive for human immunodeficiency virus (HIV). The most common include PNEUMOCYSTIS PNEUMONIA, Kaposi's sarcoma, cryptosporidiosis, herpes simplex, toxoplasmosis, cryptococcosis, and infections with Mycobacterium avium complex, Microsporidium, and Cytomegalovirus. | 0 | 7.96 | 19 | 2 |
Amyoplasia Congenita [description not available] | 0 | 2.44 | 2 | 0 |
Lipomatosis A disorder characterized by the accumulation of encapsulated or unencapsulated tumor-like fatty tissue resembling LIPOMA. | 0 | 3.71 | 3 | 0 |
Serotonin Syndrome An adverse drug interaction characterized by altered mental status, autonomic dysfunction, and neuromuscular abnormalities. It is most frequently caused by use of both serotonin reuptake inhibitors and monoamine oxidase inhibitors, leading to excess serotonin availability in the CNS at the serotonin 1A receptor. | 0 | 2.13 | 1 | 0 |
Bartonella henselae Infection [description not available] | 0 | 2.9 | 4 | 0 |
Cat-Scratch Disease A self-limiting bacterial infection of the regional lymph nodes caused by AFIPIA felis, a gram-negative bacterium recently identified by the Centers for Disease Control and Prevention and by BARTONELLA HENSELAE. It usually arises one or more weeks following a feline scratch, with raised inflammatory nodules at the site of the scratch being the primary symptom. | 0 | 2.9 | 4 | 0 |
Gangliocytoma [description not available] | 0 | 3.28 | 2 | 0 |
Cancer of Liver [description not available] | 0 | 5.29 | 9 | 0 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 5.29 | 9 | 0 |
Cancer of Nose [description not available] | 0 | 5.31 | 13 | 0 |
Tauopathies Neurodegenerative disorders involving deposition of abnormal tau protein isoforms (TAU PROTEINS) in neurons and glial cells in the brain. Pathological aggregations of tau proteins are associated with mutation of the tau gene on chromosome 17 in patients with ALZHEIMER DISEASE; DEMENTIA; PARKINSONIAN DISORDERS; progressive supranuclear palsy (SUPRANUCLEAR PALSY, PROGRESSIVE); and corticobasal degeneration. | 0 | 3.01 | 4 | 0 |
Dysplastic Nevus Syndrome, Hereditary [description not available] | 0 | 2.13 | 1 | 0 |
Epithelial Neoplasms [description not available] | 0 | 3.87 | 2 | 0 |
Posterior Capsular Rupture, Ocular A breach in the continuity of the posterior chamber of the eyeball. | 0 | 2.13 | 1 | 0 |
Artificial Intra-ocular Implant Dislocation [description not available] | 0 | 2.13 | 1 | 0 |
Duncan Disease [description not available] | 0 | 3.88 | 4 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 3.88 | 4 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 3.35 | 7 | 0 |
Glioblastoma A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures. | 0 | 8.35 | 7 | 0 |
Hyperlipoproteinemia [description not available] | 0 | 8.62 | 3 | 0 |
Hyperlipoproteinemias Conditions with abnormally elevated levels of LIPOPROTEINS in the blood. They may be inherited, acquired, primary, or secondary. Hyperlipoproteinemias are classified according to the pattern of lipoproteins on electrophoresis or ultracentrifugation. | 0 | 3.62 | 3 | 0 |
Impaired Glucose Tolerance [description not available] | 0 | 2.13 | 1 | 0 |
Acanthosis Nigricans A circumscribed melanosis consisting of a brown-pigmented, velvety verrucosity or fine papillomatosis appearing in the axillae and other body folds. It occurs in association with endocrine disorders, underlying malignancy, administration of certain drugs, or as in inherited disorder. | 0 | 2.38 | 2 | 0 |
Glucose Intolerance A pathological state in which BLOOD GLUCOSE level is less than approximately 140 mg/100 ml of PLASMA at fasting, and above approximately 200 mg/100 ml plasma at 30-, 60-, or 90-minute during a GLUCOSE TOLERANCE TEST. This condition is seen frequently in DIABETES MELLITUS, but also occurs with other diseases and MALNUTRITION. | 0 | 2.13 | 1 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 7.29 | 23 | 2 |
Carcinoma A malignant neoplasm made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. It is a histological type of neoplasm and not a synonym for cancer. | 0 | 12.29 | 23 | 2 |
Drug Refractory Epilepsy [description not available] | 0 | 2.13 | 1 | 0 |
Abdominal Epilepsy [description not available] | 0 | 2.42 | 2 | 0 |
Epilepsies, Partial Conditions characterized by recurrent paroxysmal neuronal discharges which arise from a focal region of the brain. Partial seizures are divided into simple and complex, depending on whether consciousness is unaltered (simple partial seizure) or disturbed (complex partial seizure). Both types may feature a wide variety of motor, sensory, and autonomic symptoms. Partial seizures may be classified by associated clinical features or anatomic location of the seizure focus. A secondary generalized seizure refers to a partial seizure that spreads to involve the brain diffusely. (From Adams et al., Principles of Neurology, 6th ed, pp317) | 0 | 2.42 | 2 | 0 |
Adolescent Myoclonic Epilepsy [description not available] | 0 | 2.13 | 1 | 0 |
Anthracosis A diffuse parenchymal lung disease caused by accumulation of inhaled CARBON or coal dust. The disease can progress from asymptomatic anthracosis to massive lung fibrosis. This lung lesion usually occurs in coal MINERS, but can be seen in urban dwellers and tobacco smokers. | 0 | 2.15 | 1 | 0 |
Bilateral Nasal Obstruction [description not available] | 0 | 5.53 | 4 | 4 |
Nasal Obstruction Any hindrance to the passage of air into and out of the nose. The obstruction may be unilateral or bilateral, and may involve any part of the NASAL CAVITY. | 0 | 5.53 | 4 | 4 |
Infections, Parvoviridae [description not available] | 0 | 2.13 | 1 | 0 |
Absence Status [description not available] | 0 | 2.13 | 1 | 0 |
Status Epilepticus A prolonged seizure or seizures repeated frequently enough to prevent recovery between episodes occurring over a period of 20-30 minutes. The most common subtype is generalized tonic-clonic status epilepticus, a potentially fatal condition associated with neuronal injury and respiratory and metabolic dysfunction. Nonconvulsive forms include petit mal status and complex partial status, which may manifest as behavioral disturbances. Simple partial status epilepticus consists of persistent motor, sensory, or autonomic seizures that do not impair cognition (see also EPILEPSIA PARTIALIS CONTINUA). Subclinical status epilepticus generally refers to seizures occurring in an unresponsive or comatose individual in the absence of overt signs of seizure activity. (From N Engl J Med 1998 Apr 2;338(14):970-6; Neurologia 1997 Dec;12 Suppl 6:25-30) | 0 | 2.13 | 1 | 0 |
Blastocyst Disintegration [description not available] | 0 | 2.47 | 2 | 0 |
Immune Reconstitution Disease [description not available] | 0 | 2.13 | 1 | 0 |
Overweight A status with BODY WEIGHT that is above certain standards. In the scale of BODY MASS INDEX, overweight is defined as having a BMI of 25.0-29.9 kg/m2. Overweight may or may not be due to increases in body fat (ADIPOSE TISSUE), hence overweight does not equal over fat. | 0 | 2.13 | 1 | 0 |
Adiadochokinesis [description not available] | 0 | 3.06 | 5 | 0 |
Cerebellar Ataxia Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90) | 0 | 8.06 | 5 | 0 |
Chromosome-Defective Micronuclei [description not available] | 0 | 2.49 | 2 | 0 |
Anaplastic Ependymoma [description not available] | 0 | 2.13 | 1 | 0 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 3.07 | 5 | 0 |
Ependymoma Glioma derived from EPENDYMOGLIAL CELLS that tend to present as malignant intracranial tumors in children and as benign intraspinal neoplasms in adults. It may arise from any level of the ventricular system or central canal of the spinal cord. Intracranial ependymomas most frequently originate in the FOURTH VENTRICLE and histologically are densely cellular tumors which may contain ependymal tubules and perivascular pseudorosettes. Spinal ependymomas are usually benign papillary or myxopapillary tumors. (From DeVita et al., Principles and Practice of Oncology, 5th ed, p2018; Escourolle et al., Manual of Basic Neuropathology, 2nd ed, pp28-9) | 0 | 7.13 | 1 | 0 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 3.07 | 5 | 0 |
Adenitis [description not available] | 0 | 3.05 | 5 | 0 |
Colitis, Granulomatous [description not available] | 0 | 3.64 | 3 | 0 |
Crohn Disease A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients. | 0 | 3.64 | 3 | 0 |
Motor Disorders Motor skills deficits that significantly and persistently interfere with ACTIVITIES OF DAILY LIVING appropriate to chronological age. (from DSM-5) | 0 | 2.13 | 1 | 0 |
Cone-Rod Degenerations [description not available] | 0 | 2.13 | 1 | 0 |
Hyperplasia, Reactive Lymphoid [description not available] | 0 | 2.13 | 1 | 0 |
Gastric Diseases [description not available] | 0 | 3.8 | 2 | 1 |
Haemonchiasis Infection with nematodes of the genus HAEMONCHUS, characterized by digestive abnormalities and anemia similar to that from hookworm infestation. | 0 | 2.77 | 3 | 0 |
Cerebrospinal Fluid Hypovolemia [description not available] | 0 | 4.11 | 3 | 1 |
Bradyarrhythmia [description not available] | 0 | 5.65 | 19 | 0 |
Mandibular Fractures Fractures of the lower jaw. | 0 | 2.39 | 2 | 0 |
Bradycardia Cardiac arrhythmias that are characterized by excessively slow HEART RATE, usually below 50 beats per minute in human adults. They can be classified broadly into SINOATRIAL NODE dysfunction and ATRIOVENTRICULAR BLOCK. | 0 | 5.65 | 19 | 0 |
Tuberculosis, Miliary An acute form of TUBERCULOSIS in which minute tubercles are formed in a number of organs of the body due to dissemination of the bacilli through the blood stream. | 0 | 4.64 | 11 | 0 |
Abscess, Intracranial, Subdural [description not available] | 0 | 2.15 | 1 | 0 |
Sarcoma, Epithelioid [description not available] | 0 | 5.63 | 19 | 0 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 10.63 | 19 | 0 |
Carotid Artery Thrombosis Blood clot formation in any part of the CAROTID ARTERIES. This may produce CAROTID STENOSIS or occlusion of the vessel, leading to TRANSIENT ISCHEMIC ATTACK; CEREBRAL INFARCTION; or AMAUROSIS FUGAX. | 0 | 4.62 | 28 | 0 |
Ataxias, Hereditary [description not available] | 0 | 3.04 | 5 | 0 |
Drug Withdrawal Symptoms [description not available] | 0 | 4.47 | 5 | 0 |
Substance Withdrawal Syndrome Physiological and psychological symptoms associated with withdrawal from the use of a drug after prolonged administration or habituation. The concept includes withdrawal from smoking or drinking, as well as withdrawal from an administered drug. | 0 | 4.47 | 5 | 0 |
Eperythrozoonosis [description not available] | 0 | 5.6 | 18 | 0 |
Brill-Symmers Disease [description not available] | 0 | 2.15 | 1 | 0 |
Lymphoma, Follicular Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES. | 0 | 2.15 | 1 | 0 |
Blood Coagulation Disorders, Inherited Hemorrhagic and thrombotic disorders that occur as a consequence of inherited abnormalities in blood coagulation. | 0 | 3.06 | 1 | 0 |
Seasonal Affective Disorders [description not available] | 0 | 5.41 | 5 | 1 |
Seasonal Affective Disorder A syndrome characterized by depressions that recur annually at the same time each year, usually during the winter months. Other symptoms include anxiety, irritability, decreased energy, increased appetite (carbohydrate cravings), increased duration of sleep, and weight gain. SAD (seasonal affective disorder) can be treated by daily exposure to bright artificial lights (PHOTOTHERAPY), during the season of recurrence. | 0 | 5.41 | 5 | 1 |
Neurogenic Inflammation Inflammation caused by an injurious stimulus of peripheral neurons and resulting in release of neuropeptides which affect vascular permeability and help initiate proinflammatory and immune reactions at the site of injury. | 0 | 2.15 | 1 | 0 |
Diarrhea An increased liquidity or decreased consistency of FECES, such as running stool. Fecal consistency is related to the ratio of water-holding capacity of insoluble solids to total water, rather than the amount of water present. Diarrhea is not hyperdefecation or increased fecal weight. | 0 | 5.65 | 19 | 0 |
Encephalopathy, Hepatic [description not available] | 0 | 2.15 | 1 | 0 |
Hepatic Encephalopathy A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5) | 0 | 7.15 | 1 | 0 |
Gestational Hypertension [description not available] | 0 | 3.38 | 2 | 0 |
Hypertension, Pregnancy-Induced A condition in pregnant women with elevated systolic ( | 0 | 3.38 | 2 | 0 |
Autoimmune Demyelinating Diseases, Central Nervous System [description not available] | 0 | 2.15 | 1 | 0 |
Rhinitis, Allergic, Nonseasonal [description not available] | 0 | 5.59 | 6 | 0 |
Rhinitis, Allergic, Perennial Inflammation of the mucous membrane of the nose similar to that found in hay fever except that symptoms persist throughout the year. The causes are usually air-borne allergens, particularly dusts, feathers, molds, animal fur, etc. | 0 | 5.59 | 6 | 0 |
Leukemia, Myeloid, Acute, M4 [description not available] | 0 | 2.4 | 2 | 0 |
Leukemia, Myelomonocytic, Acute A pediatric acute myeloid leukemia involving both myeloid and monocytoid precursors. At least 20% of non-erythroid cells are of monocytic origin. | 0 | 2.4 | 2 | 0 |
Cot Death [description not available] | 0 | 2.4 | 2 | 0 |
Abnormalities, Autosome [description not available] | 0 | 8.92 | 64 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 2.64 | 3 | 0 |
Boils [description not available] | 0 | 2.65 | 3 | 0 |
Allergic Encephalomyelitis [description not available] | 0 | 4.6 | 10 | 0 |
Beuren Syndrome [description not available] | 0 | 2.71 | 3 | 0 |
Sterility, Male [description not available] | 0 | 3.37 | 7 | 0 |
Muscular Dystrophy, Animal MUSCULAR DYSTROPHY that occurs in VERTEBRATE animals. | 0 | 2.74 | 3 | 0 |
Infertility, Male The inability of the male to effect FERTILIZATION of an OVUM after a specified period of unprotected intercourse. Male sterility is permanent infertility. | 0 | 3.37 | 7 | 0 |
Cadmium Poisoning Poisoning occurring after exposure to cadmium compounds or fumes. It may cause gastrointestinal syndromes, anemia, or pneumonitis. | 0 | 2.04 | 1 | 0 |
Hydrophobia [description not available] | 0 | 4.27 | 7 | 0 |
Avian Flu [description not available] | 0 | 2.45 | 2 | 0 |
Influenza in Birds Infection of domestic and wild fowl and other BIRDS with INFLUENZA A VIRUS. Avian influenza usually does not sicken birds, but can be highly pathogenic and fatal in domestic POULTRY. | 0 | 2.45 | 2 | 0 |
Community Acquired Infection [description not available] | 0 | 2.76 | 3 | 0 |
Happy Puppet Syndrome [description not available] | 0 | 2.44 | 2 | 0 |
Angelman Syndrome A syndrome characterized by multiple abnormalities, MENTAL RETARDATION, and movement disorders. Present usually are skull and other abnormalities, frequent infantile spasms (SPASMS, INFANTILE); easily provoked and prolonged paroxysms of laughter (hence happy); jerky puppetlike movements (hence puppet); continuous tongue protrusion; motor retardation; ATAXIA; MUSCLE HYPOTONIA; and a peculiar facies. It is associated with maternal deletions of chromosome 15q11-13 and other genetic abnormalities. (From Am J Med Genet 1998 Dec 4;80(4):385-90; Hum Mol Genet 1999 Jan;8(1):129-35) | 0 | 2.44 | 2 | 0 |
Lead Encephalopathy, Childhood [description not available] | 0 | 2.05 | 1 | 0 |
Atopic Hypersensitivity [description not available] | 0 | 5.62 | 10 | 0 |
Psychophysiologic Disorders A group of disorders characterized by physical symptoms that are affected by emotional factors and involve a single organ system, usually under AUTONOMIC NERVOUS SYSTEM control. (American Psychiatric Glossary, 1988) | 0 | 4.25 | 4 | 0 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 5.9 | 25 | 0 |
Anhidrosis [description not available] | 0 | 2.43 | 2 | 0 |
Borna Disease An encephalomyelitis of horses, sheep and cattle caused by BORNA DISEASE VIRUS. | 0 | 2.89 | 4 | 0 |
Atrophic Muscular Disorders [description not available] | 0 | 2.45 | 2 | 0 |
Anhidrotic Ectodermal Dysplasia [description not available] | 0 | 4.57 | 10 | 0 |
Hemangiopericytoma A tumor composed of spindle cells with a rich vascular network, which apparently arises from pericytes, cells of smooth muscle origin that lie around small vessels. Benign and malignant hemangiopericytomas exist, and the rarity of these lesions has led to considerable confusion in distinguishing between benign and malignant variants. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1364) | 0 | 3.33 | 2 | 0 |
Dyslipidemia [description not available] | 0 | 2.44 | 2 | 0 |
Dyslipidemias Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL, high TRIGLYCERIDES, low HIGH DENSITY LIPOPROTEIN CHOLESTEROL, and elevated LOW DENSITY LIPOPROTEIN CHOLESTEROL. | 0 | 2.44 | 2 | 0 |
CBS Deficiency [description not available] | 0 | 3.35 | 7 | 0 |
Inborn Errors of Metabolism [description not available] | 0 | 5.52 | 9 | 0 |
Homocystinuria Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979) | 0 | 3.35 | 7 | 0 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 5.52 | 9 | 0 |
Cardio-Cutaneous Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Borrelia hermsii Infection [description not available] | 0 | 2.62 | 3 | 0 |
Deficiency Diseases A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 10.59 | 30 | 0 |
Hemiplegia, Crossed [description not available] | 0 | 3.54 | 9 | 0 |
Hemiplegia Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body. | 0 | 3.54 | 9 | 0 |
Poisoning, Mercury [description not available] | 0 | 2.85 | 4 | 0 |
Mercury Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of MERCURY or MERCURY COMPOUNDS. | 0 | 7.85 | 4 | 0 |
Congenital Rubella Syndrome [description not available] | 0 | 1.92 | 1 | 0 |
Ileus A condition caused by the lack of intestinal PERISTALSIS or INTESTINAL MOTILITY without any mechanical obstruction. This interference of the flow of INTESTINAL CONTENTS often leads to INTESTINAL OBSTRUCTION. Ileus may be classified into postoperative, inflammatory, metabolic, neurogenic, and drug-induced. | 0 | 1.92 | 1 | 0 |
Pus [description not available] | 0 | 3.81 | 12 | 0 |
Uveitis, Suppurative Intraocular infection caused mainly by pus-producing bacteria and rarely by fungi. The infection may be caused by an injury or surgical wound (exogenous) or by endogenous septic emboli in such diseases as bacterial endocarditis or meningococcemia. | 0 | 1.92 | 1 | 0 |
Meningitis, Tuberculous [description not available] | 0 | 5.21 | 52 | 0 |
Tuberculosis, Meningeal A form of bacterial meningitis caused by MYCOBACTERIUM TUBERCULOSIS or rarely MYCOBACTERIUM BOVIS. The organism seeds the meninges and forms microtuberculomas which subsequently rupture. The clinical course tends to be subacute, with progressions occurring over a period of several days or longer. Headache and meningeal irritation may be followed by SEIZURES, cranial neuropathies, focal neurologic deficits, somnolence, and eventually COMA. The illness may occur in immunocompetent individuals or as an OPPORTUNISTIC INFECTION in the ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunodeficiency syndromes. (From Adams et al., Principles of Neurology, 6th ed, pp717-9) | 0 | 5.21 | 52 | 0 |
Complications, Labor [description not available] | 0 | 2.85 | 4 | 0 |
Neuroses [description not available] | 0 | 4.07 | 16 | 0 |
Neurotic Disorders Disorders in which the symptoms are distressing to the individual and recognized by him or her as being unacceptable. Social relationships may be greatly affected but usually remain within acceptable limits. The disturbance is relatively enduring or recurrent without treatment. | 0 | 4.07 | 16 | 0 |
Vaccinia The cutaneous and occasional systemic reactions associated with vaccination using smallpox (variola) vaccine. | 0 | 3.95 | 5 | 0 |
Paraganglioma, Gangliocytic [description not available] | 0 | 2.62 | 3 | 0 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 4.11 | 6 | 0 |
Paraganglioma A neural crest tumor usually derived from the chromoreceptor tissue of a paraganglion, such as the carotid body, or medulla of the adrenal gland (usually called a chromaffinoma or pheochromocytoma). It is more common in women than in men. (Stedman, 25th ed; from Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.62 | 3 | 0 |
Pheochromocytoma A usually benign, well-encapsulated, lobular, vascular tumor of chromaffin tissue of the ADRENAL MEDULLA or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of EPINEPHRINE and NOREPINEPHRINE, is HYPERTENSION, which may be persistent or intermittent. During severe attacks, there may be HEADACHE; SWEATING, palpitation, apprehension, TREMOR; PALLOR or FLUSHING of the face, NAUSEA and VOMITING, pain in the CHEST and ABDOMEN, and paresthesias of the extremities. The incidence of malignancy is as low as 5% but the pathologic distinction between benign and malignant pheochromocytomas is not clear. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1298) | 0 | 4.11 | 6 | 0 |
Elaeophoriasis [description not available] | 0 | 5 | 16 | 0 |
Filariasis Infections with nematodes of the superfamily FILARIOIDEA. The presence of living worms in the body is mainly asymptomatic but the death of adult worms leads to granulomatous inflammation and permanent fibrosis. Organisms of the genus Elaeophora infect wild elk and domestic sheep causing ischemic necrosis of the brain, blindness, and dermatosis of the face. | 0 | 5 | 16 | 0 |
Brill Disease [description not available] | 0 | 3.02 | 5 | 0 |
Typhus, Epidemic Louse-Borne The classic form of typhus, caused by RICKETTSIA PROWAZEKII, which is transmitted from man to man by the louse Pediculus humanus corporis. This disease is characterized by the sudden onset of intense headache, malaise, and generalized myalgia followed by the formation of a macular skin eruption and vascular and neurologic disturbances. | 0 | 3.02 | 5 | 0 |
Xanthoma [description not available] | 0 | 3.18 | 6 | 0 |
Mikulicz Disease [description not available] | 0 | 2.84 | 4 | 0 |
Blood Diseases [description not available] | 0 | 6.04 | 21 | 0 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 6.04 | 21 | 0 |
Scrofuloderma [description not available] | 0 | 2.84 | 4 | 0 |
Tooth Diseases Diseases involving the TEETH. | 0 | 3.32 | 7 | 0 |
Laryngeal Diseases Pathological processes involving any part of the LARYNX which coordinates many functions such as voice production, breathing, swallowing, and coughing. | 0 | 1.92 | 1 | 0 |
Sprains [description not available] | 0 | 1.92 | 1 | 0 |
Sprains and Strains A collective term for muscle and ligament injuries without dislocation or fracture. A sprain is a joint injury in which some of the fibers of a supporting ligament are ruptured but the continuity of the ligament remains intact. A strain is an overstretching or overexertion of some part of the musculature. | 0 | 1.92 | 1 | 0 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 8.38 | 26 | 1 |
Glial Cell Tumors [description not available] | 0 | 5.96 | 27 | 0 |
Cancer of Parotid [description not available] | 0 | 2.63 | 3 | 0 |
Glioma Benign and malignant central nervous system neoplasms derived from glial cells (i.e., astrocytes, oligodendrocytes, and ependymocytes). Astrocytes may give rise to astrocytomas (ASTROCYTOMA) or glioblastoma multiforme (see GLIOBLASTOMA). Oligodendrocytes give rise to oligodendrogliomas (OLIGODENDROGLIOMA) and ependymocytes may undergo transformation to become EPENDYMOMA; CHOROID PLEXUS NEOPLASMS; or colloid cysts of the third ventricle. (From Escourolle et al., Manual of Basic Neuropathology, 2nd ed, p21) | 0 | 5.96 | 27 | 0 |
Parotid Neoplasms Tumors or cancer of the PAROTID GLAND. | 0 | 2.63 | 3 | 0 |
Metabolic Acidosis [description not available] | 0 | 3.06 | 5 | 0 |
Acidosis A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up. | 0 | 3.06 | 5 | 0 |
Endotoxin Shock [description not available] | 0 | 4.49 | 3 | 0 |
Shock, Septic Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status. | 0 | 4.49 | 3 | 0 |
Black Death [description not available] | 0 | 2.04 | 1 | 0 |
Plague An acute infectious disease caused by YERSINIA PESTIS that affects humans, wild rodents, and their ectoparasites. This condition persists due to its firm entrenchment in sylvatic rodent-flea ecosystems throughout the world. Bubonic plague is the most common form. | 0 | 2.04 | 1 | 0 |
Cervicitis [description not available] | 0 | 2.05 | 1 | 0 |
Condition, Preneoplastic [description not available] | 0 | 2.89 | 4 | 0 |
Donovanosis [description not available] | 0 | 2.05 | 1 | 0 |
Uterine Cervicitis Inflammation of the UTERINE CERVIX. | 0 | 2.05 | 1 | 0 |
Granuloma Inguinale Anogenital ulcers caused by Calymmatobacterium granulomatis as distinguished from lymphogranuloma inguinale (see LYMPHOGRANULOMA VENEREUM) caused by CHLAMYDIA TRACHOMATIS. Diagnosis is made by demonstration of typical intracellular Donovan bodies in crushed-tissue smears. | 0 | 2.05 | 1 | 0 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 2.89 | 4 | 0 |
Clostridioides difficile Infection [description not available] | 0 | 3.8 | 4 | 0 |
Clostridium Infections Infections with bacteria of the genus CLOSTRIDIUM and closely related CLOSTRIDIOIDES species. | 0 | 3.8 | 4 | 0 |
Fasciitis, Necrotizing A fulminating bacterial infection of the deep layers of the skin and FASCIA. It can be caused by many different organisms, with STREPTOCOCCUS PYOGENES being the most common. | 0 | 2.05 | 1 | 0 |
Freckle, Melanotic [description not available] | 0 | 2.05 | 1 | 0 |
Eyelid Neoplasms Tumors of cancer of the EYELIDS. | 0 | 5.91 | 25 | 0 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 4.79 | 5 | 0 |
Cochlear Diseases Pathological processes of the snail-like structure (COCHLEA) of the inner ear (LABYRINTH) which can involve its nervous tissue, blood vessels, or fluid (ENDOLYMPH). | 0 | 2.05 | 1 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 2.44 | 2 | 0 |
Muscular Dystrophy, Duchenne An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) | 0 | 2.44 | 2 | 0 |
Aneuploid [description not available] | 0 | 2.42 | 2 | 0 |
Chromosomal Triplication [description not available] | 0 | 4.59 | 27 | 0 |
DDD MPGNII [description not available] | 0 | 2.93 | 4 | 0 |
Glomerulonephritis, Membranoproliferative Chronic glomerulonephritis characterized histologically by proliferation of MESANGIAL CELLS, increase in the MESANGIAL EXTRACELLULAR MATRIX, and a thickening of the glomerular capillary walls. This may appear as a primary disorder or secondary to other diseases including infections and autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Various subtypes are classified by their abnormal ultrastructures and immune deposits. Hypocomplementemia is a characteristic feature of all types of MPGN. | 0 | 2.93 | 4 | 0 |
Cholera Infantum [description not available] | 0 | 6.6 | 12 | 1 |
Injuries, Tendon [description not available] | 0 | 2.96 | 1 | 0 |
Encephalomyelitis, Inflammatory [description not available] | 0 | 3.44 | 8 | 0 |
Encephalomyelitis A general term indicating inflammation of the BRAIN and SPINAL CORD, often used to indicate an infectious process, but also applicable to a variety of autoimmune and toxic-metabolic conditions. There is significant overlap regarding the usage of this term and ENCEPHALITIS in the literature. | 0 | 3.44 | 8 | 0 |
Iris Neoplasms Tumors of the iris characterized by increased pigmentation of melanocytes. Iris nevi are composed of proliferated melanocytes and are associated with neurofibromatosis and malignant melanoma of the choroid and ciliary body. Malignant melanoma of the iris often originates from preexisting nevi. | 0 | 3.66 | 10 | 0 |
Acinetobacter Infections Infections with bacteria of the genus ACINETOBACTER. | 0 | 2.45 | 2 | 0 |
Acquired Encephalocele [description not available] | 0 | 3.22 | 6 | 0 |
Cerebrospinal Fluid Rhinorrhea Discharge of cerebrospinal fluid through the nose. Common etiologies include trauma, neoplasms, and prior surgery, although the condition may occur spontaneously. (Otolaryngol Head Neck Surg 1997 Apr;116(4):442-9) | 0 | 2.05 | 1 | 0 |
Mulibrey Nanism Growth failure from birth that is due to mutations in a gene (TRIM37) on chromosome 17q22-q23 which encodes a RING-B-box-coiled-coil protein. | 0 | 2.05 | 1 | 0 |
Albinism, Ocular Albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. The classic type is X-linked (Nettleship-Falls), but an autosomal recessive form also exists. Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity. | 0 | 5.23 | 12 | 0 |
MPTP Neurotoxicity Syndrome [description not available] | 0 | 2.46 | 2 | 0 |
Encephalomyelitis, Subacute Necrotizing [description not available] | 0 | 2.4 | 2 | 0 |
Leigh Disease A group of metabolic disorders primarily of infancy characterized by the subacute onset of psychomotor retardation, hypotonia, ataxia, weakness, vision loss, eye movement abnormalities, seizures, dysphagia, and lactic acidosis. Pathological features include spongy degeneration of the neuropile of the basal ganglia, thalamus, brain stem, and spinal cord. Patterns of inheritance include X-linked recessive, autosomal recessive, and mitochondrial. Leigh disease has been associated with mutations in genes for the PYRUVATE DEHYDROGENASE COMPLEX; CYTOCHROME-C OXIDASE; ATP synthase subunit 6; and subunits of mitochondrial complex I. (From Menkes, Textbook of Child Neurology, 5th ed, p850). | 0 | 2.4 | 2 | 0 |
Destombes-Rosai-Dorfman Syndrome [description not available] | 0 | 3.32 | 2 | 0 |
Histiocytosis, Sinus Benign, non-Langerhans-cell, histiocytic proliferative disorder that primarily affects the lymph nodes. It is often referred to as sinus histiocytosis with massive lymphadenopathy. | 0 | 3.32 | 2 | 0 |
Bronchiolitis, Exudative [description not available] | 0 | 2.05 | 1 | 0 |
Bronchiolitis Obliterans Inflammation of the BRONCHIOLES leading to an obstructive lung disease. Bronchioles are characterized by fibrous granulation tissue with bronchial exudates in the lumens. Clinical features include a nonproductive cough and DYSPNEA. | 0 | 2.05 | 1 | 0 |
Acquired Neuromyotonia [description not available] | 0 | 2.05 | 1 | 0 |
Dysplasia Linguofacialis [description not available] | 0 | 2.05 | 1 | 0 |
Abnormalities, Jaw [description not available] | 0 | 2.65 | 3 | 0 |
Prognathism A condition marked by abnormal protrusion of the mandible. (Dorland, 27th ed) | 0 | 2.45 | 2 | 0 |
Fetal Growth Restriction [description not available] | 0 | 3.61 | 3 | 0 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 3.61 | 3 | 0 |
Aortic Dissection [description not available] | 0 | 2.96 | 1 | 0 |
Basilar Artery Insufficiency [description not available] | 0 | 3.8 | 4 | 0 |
Multiple Neurofibromas [description not available] | 0 | 4.93 | 15 | 0 |
Neurofibromatoses A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72) | 0 | 4.93 | 15 | 0 |
Angiitis, Central Nervous System [description not available] | 0 | 2.05 | 1 | 0 |
Claustrophobia [description not available] | 0 | 2.89 | 4 | 0 |
Phobic Disorders Anxiety disorders in which the essential feature is persistent and irrational fear of a specific object, activity, or situation that the individual feels compelled to avoid. The individual recognizes the fear as excessive or unreasonable. | 0 | 2.89 | 4 | 0 |
Gasser Syndrome [description not available] | 0 | 2.96 | 4 | 0 |
Hemolytic-Uremic Syndrome A syndrome that is associated with microvascular diseases of the KIDNEY, such as RENAL CORTICAL NECROSIS. It is characterized by hemolytic anemia (ANEMIA, HEMOLYTIC); THROMBOCYTOPENIA; and ACUTE RENAL FAILURE. | 0 | 2.96 | 4 | 0 |
Aneurysm, Coronary [description not available] | 0 | 2.46 | 2 | 0 |
Lethargy A general state of sluggishness, listless, or uninterested, with being tired, and having difficulty concentrating and doing simple tasks. It may be related to DEPRESSION or DRUG ADDICTION. | 0 | 2.05 | 1 | 0 |
Animal Diseases Diseases that occur in VERTEBRATE animals. | 0 | 3.99 | 5 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 3.78 | 11 | 0 |
Cancer, Second Primary [description not available] | 0 | 4.26 | 7 | 0 |
Neoplasm Seeding The local implantation of tumor cells by contamination of instruments and surgical equipment during and after surgical resection, resulting in local growth of the cells and tumor formation. | 0 | 2.96 | 1 | 0 |
Parasitemia The presence of parasites (especially malarial parasites) in the blood. (Dorland, 27th ed) | 0 | 2.43 | 2 | 0 |
Infections, Respiratory Syncytial Virus [description not available] | 0 | 2.44 | 2 | 0 |
Respiratory Syncytial Virus Infections Pneumovirus infections caused by the RESPIRATORY SYNCYTIAL VIRUSES. Humans and cattle are most affected but infections in goats and sheep have been reported. | 0 | 2.44 | 2 | 0 |
Mouth Ulcer [description not available] | 0 | 2.05 | 1 | 0 |
Oral Ulcer A loss of mucous substance of the mouth showing local excavation of the surface, resulting from the sloughing of inflammatory necrotic tissue. It is the result of a variety of causes, e.g., denture irritation, aphthous stomatitis (STOMATITIS, APHTHOUS); NOMA; necrotizing gingivitis (GINGIVITIS, NECROTIZING ULCERATIVE); TOOTHBRUSHING; and various irritants. (From Jablonski, Dictionary of Dentistry, 1992, p842) | 0 | 2.05 | 1 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 4.88 | 8 | 0 |
Chloroma [description not available] | 0 | 2.74 | 3 | 0 |
Angiosarcoma [description not available] | 0 | 2.66 | 3 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 3.82 | 4 | 0 |
Hemangiosarcoma A rare malignant neoplasm characterized by rapidly proliferating, extensively infiltrating, anaplastic cells derived from blood vessels and lining irregular blood-filled or lumpy spaces. (Stedman, 25th ed) | 0 | 2.66 | 3 | 0 |
Osteosarcoma A sarcoma originating in bone-forming cells, affecting the ends of long bones. It is the most common and most malignant of sarcomas of the bones, and occurs chiefly among 10- to 25-year-old youths. (From Stedman, 25th ed) | 0 | 3.82 | 4 | 0 |
Soft Tissue Neoplasms Neoplasms of whatever cell type or origin, occurring in the extraskeletal connective tissue framework of the body including the organs of locomotion and their various component structures, such as nerves, blood vessels, lymphatics, etc. | 0 | 2.39 | 2 | 0 |
Sarcoma, Myeloid An extramedullary tumor of immature MYELOID CELLS or MYELOBLASTS. Granulocytic sarcoma usually occurs with or follows the onset of ACUTE MYELOID LEUKEMIA. | 0 | 2.74 | 3 | 0 |
Rida [description not available] | 0 | 4.77 | 7 | 0 |
Chronic Wasting Disease [description not available] | 0 | 2.96 | 1 | 0 |
Pyometra An accumulation of PUS in the uterine cavity (UTERUS). Pyometra generally indicates the presence of infections. | 0 | 2.05 | 1 | 0 |
Apnea, Sleep [description not available] | 0 | 5.03 | 3 | 1 |
Sleep Apnea Syndromes Disorders characterized by multiple cessations of respirations during sleep that induce partial arousals and interfere with the maintenance of sleep. Sleep apnea syndromes are divided into central (see SLEEP APNEA, CENTRAL), obstructive (see SLEEP APNEA, OBSTRUCTIVE), and mixed central-obstructive types. | 0 | 5.03 | 3 | 1 |
Allodynia [description not available] | 0 | 2.71 | 3 | 0 |
Adenoma, Oxyphilic A usually benign glandular tumor composed of oxyphil cells, large cells with small irregular nuclei and dense acidophilic granules due to the presence of abundant MITOCHONDRIA. Oxyphil cells, also known as oncocytes, are found in oncocytomas of the kidney, salivary glands, and endocrine glands. In the thyroid gland, oxyphil cells are known as Hurthle cells and Askanazy cells. | 0 | 3.34 | 2 | 0 |
Arrhythmia, Sinoatrial [description not available] | 0 | 4.48 | 3 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 3.46 | 8 | 0 |
Diabetic Nephropathies KIDNEY injuries associated with diabetes mellitus and affecting KIDNEY GLOMERULUS; ARTERIOLES; KIDNEY TUBULES; and the interstitium. Clinical signs include persistent PROTEINURIA, from microalbuminuria progressing to ALBUMINURIA of greater than 300 mg/24 h, leading to reduced GLOMERULAR FILTRATION RATE and END-STAGE RENAL DISEASE. | 0 | 3.46 | 8 | 0 |
Body Weight, Fetal [description not available] | 0 | 2.45 | 2 | 0 |
Abnormalities, Musculoskeletal [description not available] | 0 | 3.34 | 7 | 0 |
Abnormalities, Drug-Induced Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment. | 0 | 7.83 | 61 | 0 |
Multiple System Atrophy Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Multiple System Atrophy A syndrome complex composed of three conditions which represent clinical variants of the same disease process: STRIATONIGRAL DEGENERATION; SHY-DRAGER SYNDROME; and the sporadic form of OLIVOPONTOCEREBELLAR ATROPHIES. Clinical features include autonomic, cerebellar, and basal ganglia dysfunction. Pathologic examination reveals atrophy of the basal ganglia, cerebellum, pons, and medulla, with prominent loss of autonomic neurons in the brain stem and spinal cord. (From Adams et al., Principles of Neurology, 6th ed, p1076; Baillieres Clin Neurol 1997 Apr;6(1):187-204; Med Clin North Am 1999 Mar;83(2):381-92) | 0 | 2.05 | 1 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 2.89 | 4 | 0 |
Carcinoma in Situ A lesion with cytological characteristics associated with invasive carcinoma but the tumor cells are confined to the epithelium of origin, without invasion of the basement membrane. | 0 | 2.89 | 4 | 0 |
Cerebral Primitive Neuroectodermal Tumor [description not available] | 0 | 3.67 | 3 | 0 |
Neuroectodermal Tumors, Primitive A group of malignant tumors of the nervous system that feature primitive cells with elements of neuronal and/or glial differentiation. Use of this term is limited by some authors to central nervous system tumors and others include neoplasms of similar origin which arise extracranially (i.e., NEUROECTODERMAL TUMORS, PRIMITIVE, PERIPHERAL). This term is also occasionally used as a synonym for MEDULLOBLASTOMA. In general, these tumors arise in the first decade of life and tend to be highly malignant. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2059) | 0 | 3.67 | 3 | 0 |
Depression, Endogenous [description not available] | 0 | 3.97 | 5 | 0 |
Depressive Disorder An affective disorder manifested by either a dysphoric mood or loss of interest or pleasure in usual activities. The mood disturbance is prominent and relatively persistent. | 0 | 3.97 | 5 | 0 |
Enterocele An intestinal HERNIA. | 0 | 4.55 | 3 | 0 |
Hernia Protrusion of tissue, structure, or part of an organ through the bone, muscular tissue, or the membrane by which it is normally contained. Hernia may involve tissues such as the ABDOMINAL WALL or the respiratory DIAPHRAGM. Hernias may be internal, external, congenital, or acquired. | 0 | 9.55 | 3 | 0 |
Muscular Dystrophy [description not available] | 0 | 10.43 | 15 | 0 |
Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. | 0 | 5.43 | 15 | 0 |
4p Deletion Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Thrombopenia [description not available] | 0 | 4.28 | 7 | 0 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 4.28 | 7 | 0 |
Foreign-Body Migration Migration of a foreign body from its original location to some other location in the body. | 0 | 5.65 | 10 | 0 |
Mongolian Blue Spot [description not available] | 0 | 2.05 | 1 | 0 |
Mumps An acute infectious disease caused by RUBULAVIRUS, spread by direct contact, airborne droplet nuclei, fomites contaminated by infectious saliva, and perhaps urine, and usually seen in children under the age of 15, although adults may also be affected. (From Dorland, 28th ed) | 0 | 3.63 | 10 | 0 |
Parotiditis [description not available] | 0 | 2.62 | 3 | 0 |
Malnourishment [description not available] | 0 | 3.53 | 9 | 0 |
Malnutrition An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement. | 0 | 8.53 | 9 | 0 |
Gas Poisoning Poisoning that results from exposure to gases such as CARBON MONOXIDE; NOBLE GASES; OXYGEN; or NATURAL GAS. | 0 | 3.32 | 7 | 0 |
Laurence-Moon Syndrome An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9) | 0 | 3.18 | 6 | 0 |
Mole, Skin [description not available] | 0 | 5.9 | 18 | 0 |
Cervical Tuberculous Lymphadenitis [description not available] | 0 | 3.03 | 5 | 0 |
Injuries, Multiple [description not available] | 0 | 2.65 | 3 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 3.94 | 14 | 0 |
Hodgkin Disease A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen. | 0 | 3.94 | 14 | 0 |
Avitaminosis A condition due to a deficiency of one or more essential vitamins. (Dorland, 27th ed) | 0 | 5.27 | 13 | 0 |
Botulism, Infantile [description not available] | 0 | 2.33 | 2 | 0 |
Botulism A disease caused by potent protein NEUROTOXINS produced by CLOSTRIDIUM BOTULINUM which interfere with the presynaptic release of ACETYLCHOLINE at the NEUROMUSCULAR JUNCTION. Clinical features include abdominal pain, vomiting, acute PARALYSIS (including respiratory paralysis), blurred vision, and DIPLOPIA. Botulism may be classified into several subtypes (e.g., food-borne, infant, wound, and others). (From Adams et al., Principles of Neurology, 6th ed, p1208) | 0 | 2.33 | 2 | 0 |
Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 3.19 | 6 | 0 |
Leukokeratosis Leukoplakic lesions related to abnormal keratin fiber formation. | 0 | 2.34 | 2 | 0 |
Leukoplakia A white patch lesion found on a MUCOUS MEMBRANE that cannot be scraped off. Leukoplakia is generally considered a precancerous condition, however its appearance may also result from a variety of HEREDITARY DISEASES. | 0 | 2.34 | 2 | 0 |
Corynebacterium diphtheriae Infection [description not available] | 0 | 3.54 | 9 | 0 |
Diphtheria A localized infection of mucous membranes or skin caused by toxigenic strains of CORYNEBACTERIUM DIPHTHERIAE. It is characterized by the presence of a pseudomembrane at the site of infection. DIPHTHERIA TOXIN, produced by C. diphtheriae, can cause myocarditis, polyneuritis, and other systemic toxic effects. | 0 | 3.54 | 9 | 0 |
Chorea Disorders [description not available] | 0 | 3.77 | 4 | 0 |
Chorea Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES. | 0 | 3.77 | 4 | 0 |
Bronchitis Inflammation of the large airways in the lung including any part of the BRONCHI, from the PRIMARY BRONCHI to the TERTIARY BRONCHI. | 0 | 2.85 | 4 | 0 |
Nutritional Disorders [description not available] | 0 | 3.89 | 13 | 0 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 3.89 | 13 | 0 |
Abnormality, Torsion [description not available] | 0 | 3.68 | 10 | 0 |
HPV Infection [description not available] | 0 | 2.46 | 2 | 0 |
Papillomavirus Infections Neoplasms of the skin and mucous membranes caused by papillomaviruses. They are usually benign but some have a high risk for malignant progression. | 0 | 2.46 | 2 | 0 |
Encephalitis, Polio [description not available] | 0 | 3.63 | 10 | 0 |
Poliomyelitis An acute infectious disease of humans, particularly children, caused by any of three serotypes of human poliovirus (POLIOVIRUS). Usually the infection is limited to the gastrointestinal tract and nasopharynx, and is often asymptomatic. The central nervous system, primarily the spinal cord, may be affected, leading to rapidly progressive paralysis, coarse FASCICULATION and hyporeflexia. Motor neurons are primarily affected. Encephalitis may also occur. The virus replicates in the nervous system, and may cause significant neuronal loss, most notably in the spinal cord. A rare related condition, nonpoliovirus poliomyelitis, may result from infections with nonpoliovirus enteroviruses. (From Adams et al., Principles of Neurology, 6th ed, pp764-5) | 0 | 3.63 | 10 | 0 |
Enteric Fever [description not available] | 0 | 2.62 | 3 | 0 |
Typhoid Fever An acute systemic febrile infection caused by SALMONELLA TYPHI, a serotype of SALMONELLA ENTERICA. | 0 | 2.62 | 3 | 0 |
Peripheral Nerve Neoplasms [description not available] | 0 | 3.79 | 4 | 0 |
Auricular Cancer [description not available] | 0 | 2.38 | 2 | 0 |
Ear Neoplasms Tumors or cancer of any part of the hearing and equilibrium system of the body (the EXTERNAL EAR, the MIDDLE EAR, and the INNER EAR). | 0 | 2.38 | 2 | 0 |
Peripheral Nervous System Neoplasms Neoplasms which arise from peripheral nerve tissue. This includes NEUROFIBROMAS; SCHWANNOMAS; GRANULAR CELL TUMORS; and malignant peripheral NERVE SHEATH NEOPLASMS. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp1750-1) | 0 | 3.79 | 4 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 6.27 | 14 | 1 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 6.27 | 14 | 1 |
Minimal Disease, Residual [description not available] | 0 | 3.36 | 2 | 0 |
African Lymphoma [description not available] | 0 | 2.94 | 1 | 0 |
Burkitt Lymphoma A form of undifferentiated malignant LYMPHOMA usually found in central Africa, but also reported in other parts of the world. It is commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass. B-cell antigens are expressed on the immature cells that make up the tumor in virtually all cases of Burkitt lymphoma. The Epstein-Barr virus (HERPESVIRUS 4, HUMAN) has been isolated from Burkitt lymphoma cases in Africa and it is implicated as the causative agent in these cases; however, most non-African cases are EBV-negative. | 0 | 2.94 | 1 | 0 |
Colitis, Mucous [description not available] | 0 | 2.05 | 1 | 0 |
Irritable Bowel Syndrome A disorder with chronic or recurrent colonic symptoms without a clearcut etiology. This condition is characterized by chronic or recurrent ABDOMINAL PAIN, bloating, MUCUS in FECES, and an erratic disturbance of DEFECATION. | 0 | 7.05 | 1 | 0 |
Leishmania Infection [description not available] | 0 | 3.33 | 7 | 0 |
Leishmaniasis A disease caused by any of a number of species of protozoa in the genus LEISHMANIA. There are four major clinical types of this infection: cutaneous (Old and New World) (LEISHMANIASIS, CUTANEOUS), diffuse cutaneous (LEISHMANIASIS, DIFFUSE CUTANEOUS), mucocutaneous (LEISHMANIASIS, MUCOCUTANEOUS), and visceral (LEISHMANIASIS, VISCERAL). | 0 | 3.33 | 7 | 0 |
Flaccid Quadriplegia [description not available] | 0 | 3.05 | 5 | 0 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 2.92 | 4 | 0 |
Leukemia, Myelogenous, Chronic, BCR-ABL Positive Clonal hematopoetic disorder caused by an acquired genetic defect in PLURIPOTENT STEM CELLS. It starts in MYELOID CELLS of the bone marrow, invades the blood and then other organs. The condition progresses from a stable, more indolent, chronic phase (LEUKEMIA, MYELOID, CHRONIC PHASE) lasting up to 7 years, to an advanced phase composed of an accelerated phase (LEUKEMIA, MYELOID, ACCELERATED PHASE) and BLAST CRISIS. | 0 | 2.92 | 4 | 0 |
Compensatory Hyperinsulinemia A GLUCOSE-induced HYPERINSULINEMIA, a marker of insulin-resistant state. It is a mechanism to compensate for reduced sensitivity to insulin. | 0 | 2.71 | 3 | 0 |
Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | 0 | 3.24 | 6 | 0 |
Hyperinsulinism A syndrome with excessively high INSULIN levels in the BLOOD. It may cause HYPOGLYCEMIA. Etiology of hyperinsulinism varies, including hypersecretion of a beta cell tumor (INSULINOMA); autoantibodies against insulin (INSULIN ANTIBODIES); defective insulin receptor (INSULIN RESISTANCE); or overuse of exogenous insulin or HYPOGLYCEMIC AGENTS. | 0 | 2.71 | 3 | 0 |
Urinary Incontinence Involuntary loss of URINE, such as leaking of urine. It is a symptom of various underlying pathological processes. Major types of incontinence include URINARY URGE INCONTINENCE and URINARY STRESS INCONTINENCE. | 0 | 3.89 | 1 | 0 |
Rhinophyma A manifestation of severe ROSACEA resulting in significant enlargement of the NOSE and occurring primarily in men. It is caused by hypertrophy of the SEBACEOUS GLANDS and surrounding CONNECTIVE TISSUE. The nose is reddened and marked with TELANGIECTASIS. | 0 | 3.28 | 2 | 0 |
Cortical Malformations, Group II [description not available] | 0 | 2.05 | 1 | 0 |
Ciliophora Infections Infections with protozoa of the phylum CILIOPHORA. | 0 | 2.05 | 1 | 0 |
Protein Folding Diseases [description not available] | 0 | 2.46 | 2 | 0 |
Uveal Diseases Diseases of the uvea. | 0 | 6.47 | 32 | 0 |
Chandler Syndrome [description not available] | 0 | 2.07 | 1 | 0 |
Corneal Endothelial Cell Damage [description not available] | 0 | 2.07 | 1 | 0 |
Leukemia, Megakaryocytic [description not available] | 0 | 2.05 | 1 | 0 |
Leukemia, Megakaryoblastic, Acute An acute myeloid leukemia in which 20-30% of the bone marrow or peripheral blood cells are of megakaryocyte lineage. MYELOFIBROSIS or increased bone marrow RETICULIN is common. | 0 | 2.05 | 1 | 0 |
Genito-urinary Cancer [description not available] | 0 | 2.06 | 1 | 0 |
Urogenital Neoplasms Tumors or cancer of the UROGENITAL SYSTEM in either the male or the female. | 0 | 2.06 | 1 | 0 |
beta-Glucuronidase Deficiency [description not available] | 0 | 2.93 | 4 | 0 |
Mucopolysaccharidosis VII Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase. | 0 | 2.93 | 4 | 0 |
Haemophilus Infections Infections with bacteria of the genus HAEMOPHILUS. | 0 | 2.89 | 4 | 0 |
Acrorenoocular Syndrome [description not available] | 0 | 3.45 | 8 | 0 |
Leukostasis Abnormal intravascular leukocyte aggregation and clumping often seen in leukemia patients. The brain and lungs are the two most commonly affected organs. This acute syndrome requires aggressive cytoreductive modalities including chemotherapy and/or leukophoresis. It is differentiated from LEUKEMIC INFILTRATION which is a neoplastic process where leukemic cells invade organs. | 0 | 2.98 | 1 | 0 |
Acute Rheumatic Fever [description not available] | 0 | 3.02 | 5 | 0 |
Goiter Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency (HYPOTHYROIDISM), or hormone overproduction (HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic (GOITER, ENDEMIC). | 0 | 3.32 | 7 | 0 |
Thyrotoxicosis A hypermetabolic syndrome caused by excess THYROID HORMONES which may come from endogenous or exogenous sources. The endogenous source of hormone may be thyroid HYPERPLASIA; THYROID NEOPLASMS; or hormone-producing extrathyroidal tissue. Thyrotoxicosis is characterized by NERVOUSNESS; TACHYCARDIA; FATIGUE; WEIGHT LOSS; heat intolerance; and excessive SWEATING. | 0 | 3.03 | 5 | 0 |
Francisella tularensis Infection [description not available] | 0 | 1.92 | 1 | 0 |
Tularemia A plague-like disease of rodents, transmissible to man. It is caused by FRANCISELLA TULARENSIS and is characterized by fever, chills, headache, backache, and weakness. | 0 | 1.92 | 1 | 0 |
Facial Injuries General or unspecified injuries to the soft tissue or bony portions of the face. | 0 | 3.73 | 11 | 0 |
Nephrosis Pathological processes of the KIDNEY without inflammatory or neoplastic components. Nephrosis may be a primary disorder or secondary complication of other diseases. It is characterized by the NEPHROTIC SYNDROME indicating the presence of PROTEINURIA and HYPOALBUMINEMIA with accompanying EDEMA. | 0 | 1.92 | 1 | 0 |
Ophthalmoplegic Migraine Childhood-onset of recurrent headaches with an oculomotor cranial nerve palsy. Typically, ABDUCENS NERVE; OCULOMOTOR NERVE; and TROCHLEAR NERVE are involved with DIPLOPIA and BLEPHAROPTOSIS. | 0 | 2.62 | 3 | 0 |
Chondroma A benign neoplasm derived from mesodermal cells that form cartilage. It may remain within the substance of a cartilage or bone (true chondroma or enchondroma) or may develop on the surface of a cartilage (ecchondroma or ecchondrosis). (Dorland, 27th ed; Stedman, 25th ed) | 0 | 2.33 | 2 | 0 |
Click-Murmur Syndrome [description not available] | 0 | 2.87 | 4 | 0 |
Cardiac Neurosis [description not available] | 0 | 2.62 | 3 | 0 |
Ophthalmia Neonatorum Acute conjunctival inflammation in the newborn, usually caused by maternal gonococcal infection. The causative agent is NEISSERIA GONORRHOEAE. The baby's eyes are contaminated during passage through the birth canal. | 0 | 5.46 | 16 | 0 |
Arsenic Encephalopathy [description not available] | 0 | 2.85 | 4 | 0 |
Hypertension, Essential [description not available] | 0 | 2.33 | 2 | 0 |
Essential Hypertension Hypertension that occurs without known cause, or preexisting renal disease. Associated polymorphisms for a number of genes have been identified, including AGT, GNB3, and ECE1. OMIM: 145500 | 0 | 2.33 | 2 | 0 |
Arachnodactyly An abnormal bone development that is characterized by extra long and slender hands and fingers, such that the clenched thumb extends beyond the ulnar side of the hand. Arachnodactyly can include feet and toes. Arachnodactyly has been associated with several gene mutations and syndromes. | 0 | 8.31 | 7 | 0 |
Hypokalemia Abnormally low potassium concentration in the blood. It may result from potassium loss by renal secretion or by the gastrointestinal route, as by vomiting or diarrhea. It may be manifested clinically by neuromuscular disorders ranging from weakness to paralysis, by electrocardiographic abnormalities (depression of the T wave and elevation of the U wave), by renal disease, and by gastrointestinal disorders. (Dorland, 27th ed) | 0 | 1.92 | 1 | 0 |
Hemoglobinuria The presence of free HEMOGLOBIN in the URINE, indicating hemolysis of ERYTHROCYTES within the vascular system. After saturating the hemoglobin-binding proteins (HAPTOGLOBINS), free hemoglobin begins to appear in the urine. | 0 | 1.92 | 1 | 0 |
Experimental Pneumococcal Meningitis [description not available] | 0 | 2.63 | 3 | 0 |
Meningitis, Pneumococcal An acute purulent infection of the meninges and subarachnoid space caused by Streptococcus pneumoniae, most prevalent in children and adults over the age of 60. This illness may be associated with OTITIS MEDIA; MASTOIDITIS; SINUSITIS; RESPIRATORY TRACT INFECTIONS; sickle cell disease (ANEMIA, SICKLE CELL); skull fractures; and other disorders. Clinical manifestations include FEVER; HEADACHE; neck stiffness; and somnolence followed by SEIZURES; focal neurologic deficits (notably DEAFNESS); and COMA. (From Miller et al., Merritt's Textbook of Neurology, 9th ed, p111) | 0 | 2.63 | 3 | 0 |
Encephalitis, Equine [description not available] | 0 | 1.92 | 1 | 0 |
Orientia tsutsugamushi Infection [description not available] | 0 | 2.62 | 3 | 0 |
Scrub Typhus An acute infectious disease caused by ORIENTIA TSUTSUGAMUSHI. It is limited to eastern and southeastern Asia, India, northern Australia, and the adjacent islands. Characteristics include the formation of a primary cutaneous lesion at the site of the bite of an infected mite, fever lasting about two weeks, and a maculopapular rash. | 0 | 2.62 | 3 | 0 |
Bilharziasis [description not available] | 0 | 3.05 | 5 | 0 |
Schistosomiasis Infection with flukes (trematodes) of the genus SCHISTOSOMA. Three species produce the most frequent clinical diseases: SCHISTOSOMA HAEMATOBIUM (endemic in Africa and the Middle East), SCHISTOSOMA MANSONI (in Egypt, northern and southern Africa, some West Indies islands, northern 2/3 of South America), and SCHISTOSOMA JAPONICUM (in Japan, China, the Philippines, Celebes, Thailand, Laos). S. mansoni is often seen in Puerto Ricans living in the United States. | 0 | 3.05 | 5 | 0 |
Eclampsia Onset of HYPERREFLEXIA; SEIZURES; or COMA in a previously diagnosed pre-eclamptic patient (PRE-ECLAMPSIA). | 0 | 3.95 | 5 | 0 |
Angioma, Cavernous A tumor-like mass with large vascular space that is filled with blood or lymph. | 0 | 2.86 | 4 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 3.27 | 6 | 0 |
Osteoporosis Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis. | 0 | 3.27 | 6 | 0 |
Congenital Limb Deformities [description not available] | 0 | 3.24 | 6 | 0 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 2.71 | 3 | 0 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 2.71 | 3 | 0 |
Cutaneous Fistula An abnormal passage or communication leading from an internal organ to the surface of the body. | 0 | 2.42 | 2 | 0 |
Decreased Muscle Tone [description not available] | 0 | 3.34 | 7 | 0 |
Blastomyces brasiliensis Infection [description not available] | 0 | 4.04 | 3 | 1 |
Milk-Alkali Syndrome [description not available] | 0 | 3.55 | 9 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 3.55 | 9 | 0 |
Nephrocalcinosis A condition characterized by calcification of the renal tissue itself. It is usually seen in distal RENAL TUBULAR ACIDOSIS with calcium deposition in the DISTAL KIDNEY TUBULES and the surrounding interstitium. Nephrocalcinosis causes RENAL INSUFFICIENCY. | 0 | 2.38 | 2 | 0 |
Arachnoidal Cerebellar Sarcoma, Circumscribed [description not available] | 0 | 2.89 | 4 | 0 |
Medulloblastoma A malignant neoplasm that may be classified either as a glioma or as a primitive neuroectodermal tumor of childhood (see NEUROECTODERMAL TUMOR, PRIMITIVE). The tumor occurs most frequently in the first decade of life with the most typical location being the cerebellar vermis. Histologic features include a high degree of cellularity, frequent mitotic figures, and a tendency for the cells to organize into sheets or form rosettes. Medulloblastoma have a high propensity to spread throughout the craniospinal intradural axis. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2060-1) | 0 | 2.89 | 4 | 0 |
Phlegmasia Alba Dolens Inflammation that is characterized by swollen, pale, and painful limb. It is usually caused by DEEP VEIN THROMBOSIS in a FEMORAL VEIN, following PARTURITION or an illness. This condition is also called milk leg or white leg. | 0 | 5.22 | 20 | 0 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 5.22 | 20 | 0 |
Maxillary Fractures Fractures of the upper jaw. | 0 | 2.43 | 2 | 0 |
Conjunctivitis, Acute Hemorrhagic A highly contagious disease characterized by subconjunctival hemorrhage, sudden swelling of the eyelids and congestion, redness, and pain in the eye. Epidemic conjunctivitis caused by Enterovirus 70 (EV-70) was first described in Africa in 1969. It is caused also by Coxsackievirus A24 variant (CA24v). Epidemics by this organism have appeared most frequently in Asia. | 0 | 2.45 | 2 | 0 |
Rhabdomyosarcoma 2 [description not available] | 0 | 2.06 | 1 | 0 |
Rhabdomyosarcoma, Alveolar A form of RHABDOMYOSARCOMA occurring mainly in adolescents and young adults, affecting muscles of the extremities, trunk, orbital region, etc. It is extremely malignant, metastasizing widely at an early stage. Few cures have been achieved and the prognosis is poor. Alveolar refers to its microscopic appearance simulating the cells of the respiratory alveolus. (Holland et al., Cancer Medicine, 3d ed, p2188) | 0 | 2.06 | 1 | 0 |
Hyperventilation A pulmonary ventilation rate faster than is metabolically necessary for the exchange of gases. It is the result of an increased frequency of breathing, an increased tidal volume, or a combination of both. It causes an excess intake of oxygen and the blowing off of carbon dioxide. | 0 | 3.2 | 6 | 0 |
Nasopharyngeal Carcinoma A carcinoma that originates in the EPITHELIUM of the NASOPHARYNX and includes four subtypes: keratinizing squamous cell, non-keratinizing, basaloid squamous cell, and PAPILLARY ADENOCARCINOMA. It is most prevalent in Southeast Asian populations and is associated with EPSTEIN-BARR VIRUS INFECTIONS. Somatic mutations associated with this cancer have been identified in NPCR, BAP1, UBAP1, ERBB2, ERBB3, MLL2, PIK3CA, KRAS, NRAS, and ARID1A genes. | 0 | 2.06 | 1 | 0 |
Rift Valley Fever An acute infection caused by the RIFT VALLEY FEVER VIRUS, an RNA arthropod-borne virus, affecting domestic animals and humans. In animals, symptoms include HEPATITIS; abortion (ABORTION, VETERINARY); and DEATH. In humans, symptoms range from those of a flu-like disease to hemorrhagic fever, ENCEPHALITIS, or BLINDNESS. | 0 | 2.07 | 1 | 0 |
Ophthalmoplegia, Progressive Supranuclear [description not available] | 0 | 2.73 | 3 | 0 |
Supranuclear Palsy, Progressive A degenerative disease of the central nervous system characterized by balance difficulties; OCULAR MOTILITY DISORDERS (supranuclear ophthalmoplegia); DYSARTHRIA; swallowing difficulties; and axial DYSTONIA. Onset is usually in the fifth decade and disease progression occurs over several years. Pathologic findings include neurofibrillary degeneration and neuronal loss in the dorsal MESENCEPHALON; SUBTHALAMIC NUCLEUS; RED NUCLEUS; pallidum; dentate nucleus; and vestibular nuclei. (From Adams et al., Principles of Neurology, 6th ed, pp1076-7) | 0 | 2.73 | 3 | 0 |
Canine Distemper [description not available] | 0 | 3.8 | 4 | 0 |
Fibrocartilaginous Dysplasia of Bone [description not available] | 0 | 3.96 | 5 | 0 |
Fibrous Dysplasia of Bone A disease of bone marked by thinning of the cortex by fibrous tissue containing bony spicules, producing pain, disability, and gradually increasing deformity. Only one bone may be involved (FIBROUS DYSPLASIA, MONOSTOTIC) or several (FIBROUS DYSPLASIA, POLYOSTOTIC). | 0 | 3.96 | 5 | 0 |
Alcohol Abuse [description not available] | 0 | 6.32 | 15 | 1 |
Alcoholism A primary, chronic disease with genetic, psychosocial, and environmental factors influencing its development and manifestations. The disease is often progressive and fatal. It is characterized by impaired control over drinking, preoccupation with the drug alcohol, use of alcohol despite adverse consequences, and distortions in thinking, most notably denial. Each of these symptoms may be continuous or periodic. (Morse & Flavin for the Joint Commission of the National Council on Alcoholism and Drug Dependence and the American Society of Addiction Medicine to Study the Definition and Criteria for the Diagnosis of Alcoholism: in JAMA 1992;268:1012-4) | 0 | 11.32 | 15 | 1 |
Oculopharyngeal Dystrophy [description not available] | 0 | 2.06 | 1 | 0 |
Muscular Dystrophy, Oculopharyngeal An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy. | 0 | 2.06 | 1 | 0 |
Developmental Psychomotor Disorders [description not available] | 0 | 2.88 | 4 | 0 |
MEA 2b [description not available] | 0 | 2.47 | 2 | 0 |
Impotence [description not available] | 0 | 5.9 | 5 | 1 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 10.9 | 5 | 1 |
Amaurosis Fugax Transient complete or partial monocular blindness due to retinal ischemia. This may be caused by emboli from the CAROTID ARTERY (usually in association with CAROTID STENOSIS) and other locations that enter the central RETINAL ARTERY. (From Adams et al., Principles of Neurology, 6th ed, p245) | 0 | 3.66 | 3 | 0 |
Urinary Tract Diseases [description not available] | 0 | 2.36 | 2 | 0 |
Growth Hormone Insensitivity Syndrome [description not available] | 0 | 2.45 | 2 | 0 |
Laron Syndrome An autosomal recessive disorder characterized by short stature, defective GROWTH HORMONE RECEPTOR, and failure to generate INSULIN-LIKE GROWTH FACTOR I by GROWTH HORMONE. Laron syndrome is not a form of primary pituitary dwarfism (GROWTH HORMONE DEFICIENCY DWARFISM) but the result of mutation of the human GHR gene on chromosome 5. | 0 | 2.45 | 2 | 0 |
Cherry Red Spot Myoclonus Syndrome [description not available] | 0 | 3.58 | 3 | 0 |
Sarcocystosis Infection of the striated muscle of mammals by parasites of the genus SARCOCYSTIS. Disease symptoms such as vomiting, diarrhea, muscle weakness, and paralysis are produced by sarcocystin, a toxin produced by the organism. | 0 | 2.06 | 1 | 0 |
Methemoglobinemia The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait). (Dorland, 27th ed) | 0 | 3.55 | 3 | 0 |
Dysesthesia [description not available] | 0 | 5.4 | 5 | 1 |
Vaginitis Inflammation of the vagina characterized by pain and a purulent discharge. | 0 | 2.06 | 1 | 0 |
Hyperactivity, Motor [description not available] | 0 | 2.88 | 4 | 0 |
Fong Disease [description not available] | 0 | 2.4 | 2 | 0 |
Adrenoleukodystrophy, Autosomal Neonatal Form [description not available] | 0 | 2.47 | 2 | 0 |
Peroxisomal Disorders A heterogeneous group of inherited metabolic disorders marked by absent or dysfunctional PEROXISOMES. Peroxisomal enzymatic abnormalities may be single or multiple. Biosynthetic peroxisomal pathways are compromised, including the ability to synthesize ether lipids and to oxidize long-chain fatty acid precursors. Diseases in this category include ZELLWEGER SYNDROME; INFANTILE REFSUM DISEASE; rhizomelic chondrodysplasia (CHONDRODYSPLASIA PUNCTATA, RHIZOMELIC); hyperpipecolic acidemia; neonatal adrenoleukodystrophy; and ADRENOLEUKODYSTROPHY (X-linked). Neurologic dysfunction is a prominent feature of most peroxisomal disorders. | 0 | 2.47 | 2 | 0 |
Menstruation, Painful [description not available] | 0 | 3.76 | 2 | 1 |
Dysmenorrhea Painful menstruation. | 0 | 8.76 | 2 | 1 |
Dermatophytoses [description not available] | 0 | 2.65 | 3 | 0 |
Tinea Fungal infection of keratinized tissues such as hair, skin and nails. The main causative fungi include MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON. | 0 | 2.65 | 3 | 0 |
Hemangioma, Capillary A dull red, firm, dome-shaped hemangioma, sharply demarcated from surrounding skin, usually located on the head and neck, which grows rapidly and generally undergoes regression and involution without scarring. It is caused by proliferation of immature capillary vessels in active stroma, and is usually present at birth or occurs within the first two or three months of life. (Dorland, 27th ed) | 0 | 2.43 | 2 | 0 |
Rhabdomyosarcoma A malignant solid tumor arising from mesenchymal tissues which normally differentiate to form striated muscle. It can occur in a wide variety of sites. It is divided into four distinct types: pleomorphic, predominantly in male adults; alveolar (RHABDOMYOSARCOMA, ALVEOLAR), mainly in adolescents and young adults; embryonal (RHABDOMYOSARCOMA, EMBRYONAL), predominantly in infants and children; and botryoidal, also in young children. It is one of the most frequently occurring soft tissue sarcomas and the most common in children under 15. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p2186; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1647-9) | 0 | 2.9 | 4 | 0 |
Adult Pelizaeus-Merzbacher Disease [description not available] | 0 | 2.06 | 1 | 0 |
Chondrodysplasia Punctata, Rhizomelic An autosomal recessive form of CHONDRODYSPLASIA PUNCTATA characterized by defective plasmalogen biosynthesis and impaired peroxisomes. Patients have shortened proximal limbs and severely disturbed endochondral bone formation. The metabolic defects associated with the impaired peroxisomes are present only in the rhizomelic form of chondrodysplasia punctata. (From Scriver et al, Metabolic Basis of Inherited Disease, 6th ed, p1497) | 0 | 2.37 | 2 | 0 |
Aesthesioneuroblastoma [description not available] | 0 | 2.42 | 2 | 0 |
Esthesioneuroblastoma, Olfactory A malignant olfactory neuroblastoma arising from the olfactory epithelium of the superior nasal cavity and cribriform plate. It is uncommon (3% of nasal tumors) and rarely is associated with the production of excess hormones (e.g., SIADH, Cushing Syndrome). It has a high propensity for multiple local recurrences and bony metastases. (From Holland et al., Cancer Medicine, 3rd ed, p1245; J Laryngol Otol 1998 Jul;112(7):628-33) | 0 | 2.42 | 2 | 0 |
Chickungunya Fever [description not available] | 0 | 2.07 | 1 | 0 |
Encephalitis, West Nile Fever [description not available] | 0 | 2.45 | 2 | 0 |
Alpha Virus Infections [description not available] | 0 | 2.07 | 1 | 0 |
West Nile Fever A mosquito-borne viral illness caused by the WEST NILE VIRUS, a FLAVIVIRUS and endemic to regions of Africa, Asia, and Europe. Common clinical features include HEADACHE; FEVER; maculopapular rash; gastrointestinal symptoms; and lymphadenopathy. MENINGITIS; ENCEPHALITIS; and MYELITIS may also occur. The disease may occasionally be fatal or leave survivors with residual neurologic deficits. (From Joynt, Clinical Neurology, 1996, Ch26, p13; Lancet 1998 Sep 5;352(9130):767-71) | 0 | 2.45 | 2 | 0 |
Chronic Hepatitis C [description not available] | 0 | 3.65 | 3 | 0 |
Anemia, Hypochromic Anemia characterized by a decrease in the ratio of the weight of hemoglobin to the volume of the erythrocyte, i.e., the mean corpuscular hemoglobin concentration is less than normal. The individual cells contain less hemoglobin than they could have under optimal conditions. Hypochromic anemia may be caused by iron deficiency from a low iron intake, diminished iron absorption, or excessive iron loss. It can also be caused by infections or other diseases, therapeutic drugs, lead poisoning, and other conditions. (Stedman, 25th ed; from Miale, Laboratory Medicine: Hematology, 6th ed, p393) | 0 | 2.98 | 1 | 0 |
Neutropenia A decrease in the number of NEUTROPHILS found in the blood. | 0 | 2.98 | 1 | 0 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 3.65 | 3 | 0 |
Hair Diseases Diseases affecting the orderly growth and persistence of hair. | 0 | 2.87 | 4 | 0 |
Chondrosarcoma A slowly growing malignant neoplasm derived from cartilage cells, occurring most frequently in pelvic bones or near the ends of long bones, in middle-aged and old people. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion or in patients with ENCHONDROMATOSIS. (Stedman, 25th ed) | 0 | 2.46 | 2 | 0 |
Chordoma A malignant tumor arising from the embryonic remains of the notochord. It is also called chordocarcinoma, chordoepithelioma, and notochordoma. (Dorland, 27th ed) | 0 | 3.33 | 7 | 0 |
Cane-Cutter Fever [description not available] | 0 | 3.88 | 13 | 0 |
Leptospirosis Infections with bacteria of the genus LEPTOSPIRA. | 0 | 8.88 | 13 | 0 |
MEA 2a [description not available] | 0 | 2.07 | 1 | 0 |
Reproductive Sterility [description not available] | 0 | 5.27 | 13 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 10.27 | 13 | 0 |
Heritable Pulmonary Arterial Hypertension [description not available] | 0 | 7.5 | 4 | 4 |
Familial Primary Pulmonary Hypertension Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease. | 0 | 7.5 | 4 | 4 |
Cardiovascular Stroke [description not available] | 0 | 3.57 | 9 | 0 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 3.57 | 9 | 0 |
Cephalgia Syndromes [description not available] | 0 | 3.36 | 2 | 0 |
Alarm Clock Headache [description not available] | 0 | 2.98 | 1 | 0 |
Analgesic Overuse Headache [description not available] | 0 | 2.98 | 1 | 0 |
Headache Disorders Various conditions with the symptom of HEADACHE. Headache disorders are classified into major groups, such as PRIMARY HEADACHE DISORDERS (based on characteristics of their headache symptoms) and SECONDARY HEADACHE DISORDERS (based on their etiologies). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 3.36 | 2 | 0 |
Habit Chorea [description not available] | 0 | 2.37 | 2 | 0 |
Chronic Motor and Vocal Tic Disorder [description not available] | 0 | 2.07 | 1 | 0 |
Tourette Syndrome A neuropsychological disorder related to alterations in DOPAMINE metabolism and neurotransmission involving frontal-subcortical neuronal circuits. Both multiple motor and one or more vocal tics need to be present with TICS occurring many times a day, nearly daily, over a period of more than one year. The onset is before age 18 and the disturbance is not due to direct physiological effects of a substance or another medical condition. The disturbance causes marked distress or significant impairment in social, occupational, or other important areas of functioning. (From DSM-IV, 1994; Neurol Clin 1997 May;15(2):357-79) | 0 | 7.07 | 1 | 0 |
Tics Habitual, repeated, rapid contraction of certain muscles, resulting in stereotyped individualized actions that can be voluntarily suppressed for only brief periods. They often involve the face, vocal cords, neck, and less often the extremities. Examples include repetitive throat clearing, vocalizations, sniffing, pursing the lips, and excessive blinking. Tics tend to be aggravated by emotional stress. When frequent they may interfere with speech and INTERPERSONAL RELATIONS. Conditions which feature frequent and prominent tics as a primary manifestation of disease are referred to as TIC DISORDERS. (From Adams et al., Principles of Neurology, 6th ed, pp109-10) | 0 | 7.37 | 2 | 0 |
Bloch-Siemens Syndrome [description not available] | 0 | 4.27 | 7 | 0 |
Infant, Small for Gestational Age An infant having a birth weight lower than expected for its gestational age. | 0 | 3.36 | 2 | 0 |
Aortic Stenosis [description not available] | 0 | 2.39 | 2 | 0 |
Aortic Valve Stenosis A pathological constriction that can occur above (supravalvular stenosis), below (subvalvular stenosis), or at the AORTIC VALVE. It is characterized by restricted outflow from the LEFT VENTRICLE into the AORTA. | 0 | 2.39 | 2 | 0 |
Cerebral Cryptococcosis [description not available] | 0 | 2.07 | 1 | 0 |
Meningitis, Cryptococcal Meningeal inflammation produced by CRYPTOCOCCUS NEOFORMANS, an encapsulated yeast that tends to infect individuals with ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunocompromised states. The organism enters the body through the respiratory tract, but symptomatic infections are usually limited to the lungs and nervous system. The organism may also produce parenchymal brain lesions (torulomas). Clinically, the course is subacute and may feature HEADACHE; NAUSEA; PHOTOPHOBIA; focal neurologic deficits; SEIZURES; cranial neuropathies; and HYDROCEPHALUS. (From Adams et al., Principles of Neurology, 6th ed, pp721-2) | 0 | 2.07 | 1 | 0 |
Angiospasm, Intracranial [description not available] | 0 | 2.99 | 1 | 0 |
Brain Emboli [description not available] | 0 | 3.96 | 5 | 0 |
Vasospasm, Intracranial Constriction of arteries in the SKULL due to sudden, sharp, and often persistent smooth muscle contraction in blood vessels. Intracranial vasospasm results in reduced vessel lumen caliber, restricted blood flow to the brain, and BRAIN ISCHEMIA that may lead to hypoxic-ischemic brain injury (HYPOXIA-ISCHEMIA, BRAIN). | 0 | 2.99 | 1 | 0 |
Bilateral Diffuse Uveal Melanocytic Proliferation, Paraneoplastic [description not available] | 0 | 2.99 | 1 | 0 |
Coronary Artery Stenosis [description not available] | 0 | 2.07 | 1 | 0 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 2.07 | 1 | 0 |
Fractures, Comminuted A fracture in which the bone is splintered or crushed into a number of pieces. | 0 | 2.07 | 1 | 0 |
Cardiac Diseases [description not available] | 0 | 5.79 | 16 | 0 |
Hypermobility, Joint [description not available] | 0 | 2.42 | 2 | 0 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 5.79 | 16 | 0 |
Arteriosclerosis Thickening and loss of elasticity of the walls of ARTERIES of all sizes. There are many forms classified by the types of lesions and arteries involved, such as ATHEROSCLEROSIS with fatty lesions in the ARTERIAL INTIMA of medium and large muscular arteries. | 0 | 8.95 | 88 | 0 |
Acute-Phase Reaction An early local inflammatory reaction to insult or injury that consists of fever, an increase in inflammatory humoral factors, and an increased synthesis by hepatocytes of a number of proteins or glycoproteins usually found in the plasma. | 0 | 3.81 | 2 | 1 |
Congenital Icthyosis Mental Retardation Spasticity Syndrome [description not available] | 0 | 3.9 | 1 | 0 |
Sjogren-Larsson Syndrome An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism. | 0 | 3.9 | 1 | 0 |
Polyomavirus Infections Infections with POLYOMAVIRUS, which are often cultured from the urine of kidney transplant patients. Excretion of BK VIRUS is associated with ureteral strictures and CYSTITIS, and that of JC VIRUS with progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL). | 0 | 2.45 | 2 | 0 |
Cutis Laxa A group of connective tissue diseases in which skin hangs in loose pendulous folds. It is believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation. Cutis laxa is usually a genetic disease, but acquired cases have been reported. (From Dorland, 27th ed) | 0 | 2.38 | 2 | 0 |
Fifth Phacomatosis [description not available] | 0 | 3.32 | 2 | 0 |
Keratocysts [description not available] | 0 | 2.99 | 1 | 0 |
Basal Cell Nevus Syndrome Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant. | 0 | 3.32 | 2 | 0 |
Angiofibroma A benign neoplasm of fibrous tissue in which there are numerous small and large, frequently dilated, vascular channels. (Stedman, 25th ed) | 0 | 7.07 | 1 | 0 |
Lemierre Disease [description not available] | 0 | 3.4 | 2 | 0 |
Embolism, Pulmonary [description not available] | 0 | 5.04 | 7 | 0 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 5.04 | 7 | 0 |
Caries, Dental [description not available] | 0 | 2.36 | 2 | 0 |
Pericementitis [description not available] | 0 | 2.07 | 1 | 0 |
Dental Caries Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp. | 0 | 2.36 | 2 | 0 |
Periodontitis Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology) | 0 | 2.07 | 1 | 0 |
Gas Gangrene A severe condition resulting from bacteria invading healthy muscle from adjacent traumatized muscle or soft tissue. The infection originates in a wound contaminated with bacteria of the genus CLOSTRIDIUM. C. perfringens accounts for the majority of cases (over eighty percent), while C. noyvi, C. septicum, and C. histolyticum cause most of the other cases. | 0 | 7.68 | 3 | 0 |
Arteriovenous Malformations Abnormal formation of blood vessels that shunt arterial blood directly into veins without passing through the CAPILLARIES. They usually are crooked, dilated, and with thick vessel walls. A common type is the congenital arteriovenous fistula. The lack of blood flow and oxygen in the capillaries can lead to tissue damage in the affected areas. | 0 | 4.5 | 9 | 0 |
Chronic Progressive Multiple Sclerosis [description not available] | 0 | 2.08 | 1 | 0 |
Multiple Sclerosis, Chronic Progressive A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 2.08 | 1 | 0 |
Eosinophilic Granuloma The most benign and common form of Langerhans-cell histiocytosis which involves localized nodular lesions predominantly of the bones but also of the gastric mucosa, small intestine, lungs, or skin, with infiltration by EOSINOPHILS. | 0 | 4.12 | 6 | 0 |
Essential Polyarteritis [description not available] | 0 | 6.8 | 25 | 0 |
Allergic Angiitis [description not available] | 0 | 3.82 | 2 | 0 |
Churg-Strauss Syndrome Widespread necrotizing angiitis with granulomas. Pulmonary involvement is frequent. Asthma or other respiratory infection may precede evidence of vasculitis. Eosinophilia and lung involvement differentiate this disease from POLYARTERITIS NODOSA. | 0 | 3.82 | 2 | 0 |
Microscopic Polyangiitis A primary systemic vasculitis of small- and some medium-sized vessels. It is characterized by a tropism for kidneys and lungs, positive association with anti-neutrophil cytoplasmic antibodies (ANCA), and a paucity of immunoglobulin deposits in vessel walls. | 0 | 3 | 1 | 0 |
Abscess, Hepatic [description not available] | 0 | 2.43 | 2 | 0 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 2.43 | 2 | 0 |
E chaffeensis Infection [description not available] | 0 | 2.44 | 2 | 0 |
Body Dysmorphic Disorders Preoccupations with appearance or self-image causing significant distress or impairment in important areas of functioning. | 0 | 3.04 | 5 | 0 |
Autonomic Failure, Progressive [description not available] | 0 | 2.01 | 1 | 0 |
Cancer of Esophagus [description not available] | 0 | 2.01 | 1 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 2.01 | 1 | 0 |
Infections, Salmonella [description not available] | 0 | 2.41 | 2 | 0 |
Cyclitis, Chronic [description not available] | 0 | 3.61 | 3 | 0 |
Panuveitis Inflammation in which both the anterior and posterior segments of the uvea are involved and a specific focus is not apparent. It is often severe and extensive and a serious threat to vision. Causes include systemic diseases such as tuberculosis, sarcoidosis, and syphilis, as well as malignancies. The intermediate segment of the eye is not involved. | 0 | 3.34 | 2 | 0 |
Uveitis, Intermediate Inflammation of the pars plana, ciliary body, and adjacent structures. | 0 | 3.61 | 3 | 0 |
Leukemia L5178 An experimental lymphocytic leukemia of mice. | 0 | 2.92 | 1 | 0 |
Cavernous Angioma, Central Nervous System [description not available] | 0 | 2.01 | 1 | 0 |
Hemangioma, Cavernous, Central Nervous System A vascular anomaly composed of a collection of large, thin walled tortuous VEINS that can occur in any part of the central nervous system but lack intervening nervous tissue. Familial occurrence is common and has been associated with a number of genes mapped to 7q, 7p and 3q. Clinical features include SEIZURES; HEADACHE; STROKE; and progressive neurological deficit. | 0 | 2.01 | 1 | 0 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 5.6 | 10 | 0 |
Signs and Symptoms Clinical manifestations that can be either objective when observed by a physician, or subjective when perceived by the patient. | 0 | 2.67 | 3 | 0 |
Oral Manifestations Disorders of the mouth attendant upon non-oral disease or injury. | 0 | 2.37 | 2 | 0 |
Congenital Disorders [description not available] | 0 | 2.38 | 2 | 0 |
Erythema Nodosum An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral. These nodules are located predominantly on the shins with less common occurrence on the thighs and forearms. They undergo characteristic color changes ending in temporary bruise-like areas. This condition usually subsides in 3-6 weeks without scarring or atrophy. | 0 | 2.65 | 3 | 0 |
Focal Neurologic Deficits [description not available] | 0 | 5.68 | 20 | 0 |
Peritoneal Diseases Pathological processes involving the PERITONEUM. | 0 | 1.98 | 1 | 0 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 3.66 | 10 | 0 |
Respiratory Insufficiency Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) | 0 | 3.66 | 10 | 0 |
Injuries, Lightning [description not available] | 0 | 2.01 | 1 | 0 |
Ascites, Chylous [description not available] | 0 | 2.01 | 1 | 0 |
Mast-Cell Sarcoma A unifocal malignant tumor that consists of atypical pathological MAST CELLS without systemic involvement. It causes local destructive growth in organs other than in skin or bone marrow. | 0 | 2.67 | 3 | 0 |
Blue-Eared Pig Disease [description not available] | 0 | 2.01 | 1 | 0 |
Mastitis, Bovine INFLAMMATION of the UDDER in cows. | 0 | 2.01 | 1 | 0 |
Central Nervous System Tuberculosis [description not available] | 0 | 2.01 | 1 | 0 |
Abscess, Tubercular, Intracranial [description not available] | 0 | 2.01 | 1 | 0 |
Iron Overload An excessive accumulation of iron in the body due to a greater than normal absorption of iron from the gastrointestinal tract or from parenteral injection. This may arise from idiopathic hemochromatosis, excessive iron intake, chronic alcoholism, certain types of refractory anemia, or transfusional hemosiderosis. (From Churchill's Illustrated Medical Dictionary, 1989) | 0 | 8.34 | 2 | 0 |
Hypesthesia Absent or reduced sensitivity to cutaneous stimulation. | 0 | 2.69 | 3 | 0 |
Closed Head Injuries [description not available] | 0 | 2.89 | 4 | 0 |
Cranial Nerve III Injury [description not available] | 0 | 3.31 | 2 | 0 |
AIDS Seroconversion [description not available] | 0 | 2.91 | 4 | 0 |
Mouth, Edentulous Total lack of teeth through disease or extraction. | 0 | 2.01 | 1 | 0 |
Bonnevie-Ullrich Syndrome This syndrome that was originally observed by Ullrich, and designated as identical to TURNER SYNDROME, related the webbing of the neck, loose skin and other anomalies of the syndrome to accumulation of fluid in the embryo starting at the head and dispersing to the extremities (as observed by Bonnevie in mice). Commonly observed at birth in Turner Syndrome and NOONAN SYNDROME; EDEMA of the extremities usually recedes by one year and is an early sign of Turner syndrome, especially in female neonates. | 0 | 2.87 | 4 | 0 |
Turner Syndrome A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant. | 0 | 2.87 | 4 | 0 |
Infections, Pasteurella [description not available] | 0 | 3.75 | 11 | 0 |
Fractures, Compound [description not available] | 0 | 2.01 | 1 | 0 |
Newcastle Disease An acute febrile, contagious, viral disease of birds caused by an AVULAVIRUS called NEWCASTLE DISEASE VIRUS. It is characterized by respiratory and nervous symptoms in fowl and is transmissible to man causing a severe, but transient conjunctivitis. | 0 | 9.14 | 17 | 0 |
Acrania [description not available] | 0 | 3.09 | 5 | 0 |
Neural Tube Defects Congenital malformations of the central nervous system and adjacent structures related to defective neural tube closure during the first trimester of pregnancy generally occurring between days 18-29 of gestation. Ectodermal and mesodermal malformations (mainly involving the skull and vertebrae) may occur as a result of defects of neural tube closure. (From Joynt, Clinical Neurology, 1992, Ch55, pp31-41) | 0 | 8.09 | 5 | 0 |
Anoxia, Brain [description not available] | 0 | 2.39 | 2 | 0 |
Bullous Dermatoses [description not available] | 0 | 4.44 | 5 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 2.42 | 2 | 0 |
Androgen Insensitivity Syndrome [description not available] | 0 | 2.01 | 1 | 0 |
Dermatitis Seborrheica [description not available] | 0 | 3.78 | 4 | 0 |
Dermatitis, Seborrheic A chronic inflammatory disease of the skin with unknown etiology. It is characterized by moderate ERYTHEMA, dry, moist, or greasy (SEBACEOUS GLAND) scaling and yellow crusted patches on various areas, especially the scalp, that exfoliate as dandruff. Seborrheic dermatitis is common in children and adolescents with HIV INFECTIONS. | 0 | 3.78 | 4 | 0 |
Hyperidrosis [description not available] | 0 | 3.33 | 2 | 0 |
Hyperhidrosis Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief cause is thought to be emotional. Generalized hyperhidrosis may be induced by a hot, humid environment, by fever, or by vigorous exercise. | 0 | 3.33 | 2 | 0 |
Salmonella Infections, Animal Infections in animals with bacteria of the genus SALMONELLA. | 0 | 2.38 | 2 | 0 |
Buschke's Scleredema [description not available] | 0 | 2.33 | 2 | 0 |
Scleredema Adultorum A diffuse, non-pitting induration of the skin of unknown etiology that occurs most commonly in association with diabetes mellitus, predominantly in females. It typically begins on the face or head and spreads to other areas of the body, sometimes involving noncutaneous tissues. Often it is preceded by any of various infections, notably staphylococcal infections. The condition resolves spontaneously, usually within two years of onset. (From Dorland, 27th ed) | 0 | 2.33 | 2 | 0 |
Blood Pressure, Low [description not available] | 0 | 5.57 | 29 | 0 |
Hypotension Abnormally low BLOOD PRESSURE that can result in inadequate blood flow to the brain and other vital organs. Common symptom is DIZZINESS but greater negative impacts on the body occur when there is prolonged depravation of oxygen and nutrients. | 0 | 5.57 | 29 | 0 |
Nephrosclerosis Hardening of the KIDNEY due to infiltration by fibrous connective tissue (FIBROSIS), usually caused by renovascular diseases or chronic HYPERTENSION. Nephrosclerosis leads to renal ISCHEMIA. | 0 | 7.85 | 4 | 0 |
Arachnoid Membrane Inflammation [description not available] | 0 | 3.18 | 6 | 0 |
Porphyria [description not available] | 0 | 3.04 | 5 | 0 |
Porphyrias A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues. | 0 | 3.04 | 5 | 0 |
Epidermal Cyst Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules. | 0 | 3.03 | 5 | 0 |
Hydroa Vacciniforme A vesicular and bullous eruption having a tendency to recur in summer during childhood and commonly appearing on sun-exposed skin. The lesions are surrounded by an erythematous zone and resemble a vaccination. (From Dorland, 27th ed) | 0 | 2.36 | 2 | 0 |
Agnosia Loss of the ability to comprehend the meaning or recognize the importance of various forms of stimulation that cannot be attributed to impairment of a primary sensory modality. Tactile agnosia is characterized by an inability to perceive the shape and nature of an object by touch alone, despite unimpaired sensation to light touch, position, and other primary sensory modalities. | 0 | 4.64 | 11 | 0 |
Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis [description not available] | 0 | 3.44 | 8 | 0 |
Deficiency, Vitamin B [description not available] | 0 | 3.44 | 8 | 0 |
Vitamin B Deficiency A condition due to deficiency in any member of the VITAMIN B COMPLEX. These B vitamins are water-soluble and must be obtained from the diet because they are easily lost in the urine. Unlike the lipid-soluble vitamins, they cannot be stored in the body fat. | 0 | 3.44 | 8 | 0 |
Arterial Inflammation [description not available] | 0 | 4.73 | 32 | 0 |
Arteriolosclerosis Thickening of the walls of small ARTERIES or ARTERIOLES due to cell proliferation or HYALINE deposition. | 0 | 4.09 | 6 | 0 |
Hyperostosis Frontalis Interna Thickening of the inner table of the frontal bone, which may be associated with hypertrichosis and obesity. It most commonly affects women near menopause. | 0 | 2.33 | 2 | 0 |
Mixed Pineocytoma-Pineoblastoma [description not available] | 0 | 3.26 | 2 | 0 |
Pinealoma Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670) | 0 | 3.26 | 2 | 0 |
Abnormalities, Severe Teratoid Marked developmental anomalies of a fetus or infant. | 0 | 4.19 | 18 | 0 |
Addison's Anemia [description not available] | 0 | 3.44 | 8 | 0 |
Labyrinthitis Inflammation of the inner ear (LABYRINTH). | 0 | 2.33 | 2 | 0 |
Bright Disease A historical classification which is no longer used. It described acute glomerulonephritis, acute nephritic syndrome, or acute nephritis. Named for Richard Bright. | 0 | 3.04 | 5 | 0 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 3.45 | 8 | 0 |
Glomerulonephritis Inflammation of the renal glomeruli (KIDNEY GLOMERULUS) that can be classified by the type of glomerular injuries including antibody deposition, complement activation, cellular proliferation, and glomerulosclerosis. These structural and functional abnormalities usually lead to HEMATURIA; PROTEINURIA; HYPERTENSION; and RENAL INSUFFICIENCY. | 0 | 3.04 | 5 | 0 |
Frontal Sinusitis Inflammation of the NASAL MUCOSA in the FRONTAL SINUS. In many cases, it is caused by an infection of the bacteria STREPTOCOCCUS PNEUMONIAE or HAEMOPHILUS INFLUENZAE. | 0 | 1.93 | 1 | 0 |
Kaposi Disease [description not available] | 0 | 4.99 | 16 | 0 |
Xeroderma Pigmentosum A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA. | 0 | 4.99 | 16 | 0 |
Benign Supratentorial Neoplasms [description not available] | 0 | 3.31 | 7 | 0 |
Erythroblastosis Fetalis [description not available] | 0 | 3.55 | 3 | 0 |
Bronze Diabetes [description not available] | 0 | 2.63 | 3 | 0 |
Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) | 0 | 2.63 | 3 | 0 |
Erythema Multiforme A skin and mucous membrane disease characterized by an eruption of macules, papules, nodules, vesicles, and/or bullae with characteristic bull's-eye lesions usually occurring on the dorsal aspect of the hands and forearms. | 0 | 3.8 | 12 | 0 |
Autoimmune Demyelinating Disease, Peripheral [description not available] | 0 | 3.26 | 2 | 0 |
Granulocytic Leukemia [description not available] | 0 | 3.55 | 9 | 0 |
Leukemia, Myeloid Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites. | 0 | 3.55 | 9 | 0 |
alpha-L-Iduronidase Deficiency [description not available] | 0 | 3.89 | 13 | 0 |
Mucopolysaccharidosis I Systemic lysosomal storage disease caused by a deficiency of alpha-L-iduronidase (IDURONIDASE) and characterized by progressive physical deterioration with urinary excretion of DERMATAN SULFATE and HEPARAN SULFATE. There are three recognized phenotypes representing a spectrum of clinical severity from severe to mild: Hurler syndrome, Hurler-Scheie syndrome and Scheie syndrome (formerly mucopolysaccharidosis V). Symptoms may include DWARFISM; hepatosplenomegaly; thick, coarse facial features with low nasal bridge; corneal clouding; cardiac complications; and noisy breathing. | 0 | 3.89 | 13 | 0 |
Cleft Spine [description not available] | 0 | 2.85 | 4 | 0 |
Focal Infection An infection at a specific location that may spread to another region of the body. | 0 | 8.54 | 9 | 0 |
Barre-Lieou Syndrome [description not available] | 0 | 2.62 | 3 | 0 |
Heavy Metal Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of HEAVY METALS. Acute and chronic exposures can cause ANEMIA; KIDNEY and LIVER damage; PULMONARY EDEMA; MEMORY LOSS and behavioral changes; bone deformities in children; and MISCARRIAGE or PREMATURE LABOR in pregnant women. | 0 | 2.33 | 2 | 0 |
Actinomyces Infections [description not available] | 0 | 1.93 | 1 | 0 |
Erythrocytosis [description not available] | 0 | 8.32 | 7 | 0 |
Deficiency, Riboflavin [description not available] | 0 | 3.32 | 7 | 0 |
Allachesthesia [description not available] | 0 | 1.93 | 1 | 0 |
(pPNET) Peripheral Primitive Neuroectodermal Tumors [description not available] | 0 | 4.02 | 15 | 0 |
Neuroectodermal Tumors, Primitive, Peripheral A group of highly cellular primitive round cell neoplasms which occur extracranially in soft tissue and bone and are derived from embryonal neural crest cells. These tumors occur primarily in children and adolescents and share a number of characteristics with EWING SARCOMA. | 0 | 4.02 | 15 | 0 |
Catatonic Rigidity [description not available] | 0 | 2.85 | 4 | 0 |
Muscle Rigidity Continuous involuntary sustained muscle contraction which is often a manifestation of BASAL GANGLIA DISEASES. When an affected muscle is passively stretched, the degree of resistance remains constant regardless of the rate at which the muscle is stretched. This feature helps to distinguish rigidity from MUSCLE SPASTICITY. (From Adams et al., Principles of Neurology, 6th ed, p73) | 0 | 2.85 | 4 | 0 |
Parathyroid Disorders [description not available] | 0 | 2.62 | 3 | 0 |
Parathyroid Diseases Pathological processes of the PARATHYROID GLANDS. They usually manifest as hypersecretion or hyposecretion of PARATHYROID HORMONE that regulates the balance of CALCIUM; PHOSPHORUS; and MAGNESIUM in the body. | 0 | 2.62 | 3 | 0 |
Mucocele A retention cyst of the salivary gland, lacrimal sac, paranasal sinuses, appendix, or gallbladder. (Stedman, 26th ed) | 0 | 3.33 | 7 | 0 |
Dysostoses Defective bone formation involving individual bones, singly or in combination. | 0 | 7.62 | 3 | 0 |
Abortion, Tubal [description not available] | 0 | 4.93 | 9 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 4.93 | 9 | 0 |
Friedreich Disease [description not available] | 0 | 2.85 | 4 | 0 |
Friedreich Ataxia An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75) | 0 | 2.85 | 4 | 0 |
Infectious Myelitis [description not available] | 0 | 5.24 | 21 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 2.62 | 3 | 0 |
Acromegaly A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80) | 0 | 7.62 | 3 | 0 |
Benign Infratentorial Neoplasms [description not available] | 0 | 1.93 | 1 | 0 |
IgA Vasculitis A systemic non-thrombocytopenic purpura caused by HYPERSENSITIVITY VASCULITIS and deposition of IGA-containing IMMUNE COMPLEXES within the blood vessels throughout the body, including those in the kidney (KIDNEY GLOMERULUS). Clinical symptoms include URTICARIA; ERYTHEMA; ARTHRITIS; GASTROINTESTINAL HEMORRHAGE; and renal involvement. Most cases are seen in children after acute upper respiratory infections. | 0 | 2.86 | 4 | 0 |
Hyperesthesia Increased sensitivity to cutaneous stimulation due to a diminished threshold or an increased response to stimuli. | 0 | 2.63 | 3 | 0 |
Arboviral Encephalitis [description not available] | 0 | 2.63 | 3 | 0 |
Deficiency, Vitamin E [description not available] | 0 | 4.11 | 6 | 0 |
Absence of Brain, Congenital [description not available] | 0 | 3.65 | 10 | 0 |
Angiomatosis A condition with multiple tumor-like lesions caused either by congenital or developmental malformations of BLOOD VESSELS, or reactive vascular proliferations, such as in bacillary angiomatosis. Angiomatosis is considered non-neoplastic. | 0 | 4.24 | 19 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 3.44 | 8 | 0 |
Pituitary Diseases Disorders involving either the ADENOHYPOPHYSIS or the NEUROHYPOPHYSIS. These diseases usually manifest as hypersecretion or hyposecretion of PITUITARY HORMONES. Neoplastic pituitary masses can also cause compression of the OPTIC CHIASM and other adjacent structures. | 0 | 3.44 | 8 | 0 |
Fibromatosis [description not available] | 0 | 2.86 | 4 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 2.86 | 4 | 0 |
Drowning Death that occurs as a result of anoxia or heart arrest, associated with immersion in liquid. | 0 | 1.92 | 1 | 0 |
Amaurotic Familial Idiocy An outdated term for Tay-Sachs disease. | 0 | 3.32 | 7 | 0 |
Tay-Sachs Disease An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry. | 0 | 3.32 | 7 | 0 |
Salivary Gland Diseases Diseases involving the SALIVARY GLANDS. | 0 | 1.93 | 1 | 0 |
Deficiency, Pyridoxine [description not available] | 0 | 3.04 | 5 | 0 |
Eosinophilia, Pulmonary [description not available] | 0 | 2.33 | 2 | 0 |
Pulmonary Eosinophilia A condition characterized by infiltration of the lung with EOSINOPHILS due to inflammation or other disease processes. Major eosinophilic lung diseases are the eosinophilic pneumonias caused by infections, allergens, or toxic agents. | 0 | 2.33 | 2 | 0 |
Albright Syndrome [description not available] | 0 | 2.33 | 2 | 0 |
Osteitis Fibrosa Cystica A fibrous degeneration, cyst formation, and the presence of fibrous nodules in bone, usually due to HYPERPARATHYROIDISM. | 0 | 2.85 | 4 | 0 |
Bone Inflammation [description not available] | 0 | 2.85 | 4 | 0 |
Fibrous Dysplasia, Polyostotic FIBROUS DYSPLASIA OF BONE affecting several bones. When melanotic pigmentation (CAFE-AU-LAIT SPOTS) and multiple endocrine hyperfunction are additionally associated it is referred to as Albright syndrome. | 0 | 2.33 | 2 | 0 |
Brazilian Spotted Fever [description not available] | 0 | 2.35 | 2 | 0 |
Boutonneuse Fever A febrile disease of the Mediterranean area, the Crimea, Africa, and India, caused by infection with RICKETTSIA CONORII. | 0 | 1.93 | 1 | 0 |
Rocky Mountain Spotted Fever An acute febrile illness caused by RICKETTSIA RICKETTSII. It is transmitted to humans by bites of infected ticks and occurs only in North and South America. Characteristics include a sudden onset with headache and chills and fever lasting about two to three weeks. A cutaneous rash commonly appears on the extremities and trunk about the fourth day of illness. | 0 | 2.35 | 2 | 0 |
Hypermyotonia [description not available] | 0 | 1.93 | 1 | 0 |
Glandular Fever [description not available] | 0 | 3.54 | 9 | 0 |
Infectious Mononucleosis A common, acute infection usually caused by the Epstein-Barr virus (HERPESVIRUS 4, HUMAN). There is an increase in mononuclear white blood cells and other atypical lymphocytes, generalized lymphadenopathy, splenomegaly, and occasionally hepatomegaly with hepatitis. | 0 | 3.54 | 9 | 0 |
Endarteritis Inflammation of the inner endothelial lining (TUNICA INTIMA) of an artery. | 0 | 2.62 | 3 | 0 |
Coccidioides immitis Infection [description not available] | 0 | 3.32 | 7 | 0 |
Coccidioidomycosis Infection with a fungus of the genus COCCIDIOIDES, endemic to the SOUTHWESTERN UNITED STATES. It is sometimes called valley fever but should not be confused with RIFT VALLEY FEVER. Infection is caused by inhalation of airborne, fungal particles known as arthroconidia, a form of FUNGAL SPORES. A primary form is an acute, benign, self-limited respiratory infection. A secondary form is a virulent, severe, chronic, progressive granulomatous disease with systemic involvement. It can be detected by use of COCCIDIOIDIN. | 0 | 3.32 | 7 | 0 |
Bends [description not available] | 0 | 2.33 | 2 | 0 |
Glomus Jugulare Tumor A paraganglioma involving the glomus jugulare, a microscopic collection of chemoreceptor tissue in the adventitia of the bulb of the jugular vein. It may cause paralysis of the vocal cords, attacks of dizziness, blackouts, and nystagmus. It is not resectable but radiation therapy is effective. It regresses slowly, but permanent control is regularly achieved. (From Dorland, 27th ed; Stedman, 25th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1603-4) | 0 | 2.34 | 2 | 0 |
Cold Fingers, Hereditary [description not available] | 0 | 4.95 | 3 | 1 |
Raynaud Disease An idiopathic vascular disorder characterized by bilateral Raynaud phenomenon, the abrupt onset of digital paleness or CYANOSIS in response to cold exposure or stress. | 0 | 4.95 | 3 | 1 |
Auricular Flutter [description not available] | 0 | 1.93 | 1 | 0 |
Atrial Flutter Rapid, irregular atrial contractions caused by a block of electrical impulse conduction in the right atrium and a reentrant wave front traveling up the inter-atrial septum and down the right atrial free wall or vice versa. Unlike ATRIAL FIBRILLATION which is caused by abnormal impulse generation, typical atrial flutter is caused by abnormal impulse conduction. As in atrial fibrillation, patients with atrial flutter cannot effectively pump blood into the lower chambers of the heart (HEART VENTRICLES). | 0 | 1.93 | 1 | 0 |
Adenoma, Prostatic [description not available] | 0 | 2.33 | 2 | 0 |
Prostatic Hyperplasia Increase in constituent cells in the PROSTATE, leading to enlargement of the organ (hypertrophy) and adverse impact on the lower urinary tract function. This can be caused by increased rate of cell proliferation, reduced rate of cell death, or both. | 0 | 2.33 | 2 | 0 |
Pallor A clinical manifestation consisting of an unnatural paleness of the skin. | 0 | 3.81 | 12 | 0 |
Exhibitionism A disorder in which fantasies about or the act of exposing the genitals to an unsuspecting stranger produces sexual excitement with no attempt at further sexual activity with the stranger. | 0 | 1.93 | 1 | 0 |
Lipidoses Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. | 0 | 4.13 | 17 | 0 |
Niemann-Pick Disease [description not available] | 0 | 3.55 | 9 | 0 |
Niemann-Pick Diseases A group of autosomal recessive disorders in which harmful quantities of lipids accumulate in the viscera and the central nervous system. They can be caused by deficiencies of enzyme activities (SPHINGOMYELIN PHOSPHODIESTERASE) or defects in intracellular transport, resulting in the accumulation of SPHINGOMYELINS and CHOLESTEROL. There are various subtypes based on their clinical and genetic differences. | 0 | 3.55 | 9 | 0 |
Human Trichinellosis [description not available] | 0 | 3.04 | 5 | 0 |
Trichinellosis An infection with TRICHINELLA. It is caused by eating raw or undercooked meat that is infected with larvae of nematode worms TRICHINELLA genus. All members of the TRICHINELLA genus can infect human in addition to TRICHINELLA SPIRALIS, the traditional etiological agent. It is distributed throughout much of the world and is re-emerging in some parts as a public health hazard and a food safety problem. | 0 | 3.04 | 5 | 0 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 1.93 | 1 | 0 |
Cancer of Mediastinum [description not available] | 0 | 1.93 | 1 | 0 |
Mediastinal Neoplasms Tumors or cancer of the MEDIASTINUM. | 0 | 1.93 | 1 | 0 |
Centriacinar Emphysema [description not available] | 0 | 1.93 | 1 | 0 |
Spondylitis Inflammation of the SPINE. This includes both arthritic and non-arthritic conditions. | 0 | 7.63 | 3 | 0 |
Abnormalities, Cardiovascular [description not available] | 0 | 4.55 | 10 | 0 |
Cardiovascular Abnormalities Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS. | 0 | 4.55 | 10 | 0 |
Hypomenorrhea [description not available] | 0 | 3.04 | 5 | 0 |
Duhring Disease [description not available] | 0 | 2.33 | 2 | 0 |
Dermatitis Herpetiformis Rare, chronic, papulo-vesicular disease characterized by an intensely pruritic eruption consisting of various combinations of symmetrical, erythematous, papular, vesicular, or bullous lesions. The disease is strongly associated with the presence of HLA-B8 and HLA-DR3 antigens. A variety of different autoantibodies has been detected in small numbers in patients with dermatitis herpetiformis. | 0 | 2.33 | 2 | 0 |
Osseous Paget's Disease [description not available] | 0 | 3.32 | 7 | 0 |
Osteitis Deformans A disease marked by repeated episodes of increased bone resorption followed by excessive attempts at repair, resulting in weakened, deformed bones of increased mass. The resultant architecture of the bone assumes a mosaic pattern in which the fibers take on a haphazard pattern instead of the normal parallel symmetry. | 0 | 3.32 | 7 | 0 |
Liver Dysfunction [description not available] | 0 | 4.74 | 12 | 0 |
Liver Diseases Pathological processes of the LIVER. | 0 | 4.74 | 12 | 0 |
Tuberculosis, Hepatic Infection of the LIVER with species of MYCOBACTERIUM, most often MYCOBACTERIUM TUBERCULOSIS. It is characterized by localized small tuberculous miliary lesions or tumor-like mass (TUBERCULOMA), and abnormalities in liver function tests. | 0 | 1.93 | 1 | 0 |
Cyanosis A bluish or purplish discoloration of the skin and mucous membranes due to an increase in the amount of deoxygenated hemoglobin in the blood or a structural defect in the hemoglobin molecule. | 0 | 1.93 | 1 | 0 |
Fallot's Tetralogy [description not available] | 0 | 2.34 | 2 | 0 |
Tetralogy of Fallot A combination of congenital heart defects consisting of four key features including VENTRICULAR SEPTAL DEFECTS; PULMONARY STENOSIS; RIGHT VENTRICULAR HYPERTROPHY; and a dextro-positioned AORTA. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing CYANOSIS. | 0 | 2.34 | 2 | 0 |
Cor Pulmonale [description not available] | 0 | 1.93 | 1 | 0 |
Granuloma Gangraenescens [description not available] | 0 | 2.33 | 2 | 0 |
Granuloma, Lethal Midline A condition that is characterized by inflammation, ulceration, and perforation of the nose and the PALATE with progressive destruction of midline facial structures. This syndrome can be manifested in several diseases including the nasal type of EXTRANODAL NK-T-CELL LYMPHOMA and GRANULOMATOSIS WITH POLYANGIITIS. | 0 | 2.33 | 2 | 0 |
Intraventricular Septal Defects [description not available] | 0 | 2.63 | 3 | 0 |
Heart Septal Defects, Ventricular Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect. | 0 | 2.63 | 3 | 0 |
Hysteria Historical term for a chronic, but fluctuating, disorder beginning in early life and characterized by recurrent and multiple somatic complaints not apparently due to physical illness. This diagnosis is not used in contemporary practice. | 0 | 3.44 | 8 | 0 |
Cranial Sinus Thrombosis [description not available] | 0 | 3.96 | 14 | 0 |
Nanism [description not available] | 0 | 5.04 | 10 | 0 |
Dwarfism A genetic or pathological condition that is characterized by short stature and undersize. Abnormal skeletal growth usually results in an adult who is significantly below the average height. | 0 | 5.04 | 10 | 0 |
Plasma Cell Tumor [description not available] | 0 | 2.34 | 2 | 0 |
Neoplasms, Plasma Cell Neoplasms associated with a proliferation of a single clone of PLASMA CELLS and characterized by the secretion of PARAPROTEINS. | 0 | 2.33 | 2 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 2.34 | 2 | 0 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 1.93 | 1 | 0 |
Injuries, Spinal [description not available] | 0 | 1.93 | 1 | 0 |
Injuries, Whiplash [description not available] | 0 | 3.03 | 5 | 0 |
Mediastinal Diseases Disorders of the mediastinum, general or unspecified. | 0 | 1.93 | 1 | 0 |
Pappataci Fever [description not available] | 0 | 6.93 | 1 | 0 |
Bone Tuberculosis [description not available] | 0 | 3.25 | 2 | 0 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 3.81 | 12 | 0 |
Embolism, Fat Blocking of a blood vessel by fat deposits in the circulation. It is often seen after fractures of large bones or after administration of CORTICOSTEROIDS. | 0 | 3.55 | 9 | 0 |
Verruca [description not available] | 0 | 1.93 | 1 | 0 |
Warts Benign epidermal proliferations or tumors; some are viral in origin. | 0 | 1.93 | 1 | 0 |
Distorted Hearing [description not available] | 0 | 5.11 | 18 | 0 |
Addison's Disease [description not available] | 0 | 2.85 | 4 | 0 |
Adrenal Gland Hypofunction [description not available] | 0 | 2.62 | 3 | 0 |
Addison Disease, X-Linked [description not available] | 0 | 2.33 | 2 | 0 |
Hypoadrenocorticism, Familial Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200 | 0 | 2.33 | 2 | 0 |
Addison Disease An adrenal disease characterized by the progressive destruction of the ADRENAL CORTEX, resulting in insufficient production of ALDOSTERONE and HYDROCORTISONE. Clinical symptoms include ANOREXIA; NAUSEA; WEIGHT LOSS; MUSCLE WEAKNESS; and HYPERPIGMENTATION of the SKIN due to increase in circulating levels of ACTH precursor hormone which stimulates MELANOCYTES. | 0 | 2.85 | 4 | 0 |
Adrenal Insufficiency Conditions in which the production of adrenal CORTICOSTEROIDS falls below the requirement of the body. Adrenal insufficiency can be caused by defects in the ADRENAL GLANDS, the PITUITARY GLAND, or the HYPOTHALAMUS. | 0 | 2.62 | 3 | 0 |
Hemorrhagic Diathesis [description not available] | 0 | 2.33 | 2 | 0 |
Hemorrhagic Disorders Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a structural flaw in the blood vessels (HEMOSTATIC DISORDERS). | 0 | 2.33 | 2 | 0 |
Cor Triatriatum A malformation of the heart in which the embryonic common PULMONARY VEIN was not incorporated into the LEFT ATRIUM leaving behind a perforated fibromuscular membrane bisecting the left atrium, a three-atrium heart. The opening between the two left atrium sections determines the degree of obstruction to pulmonary venous return, pulmonary venous and pulmonary arterial hypertension. | 0 | 1.93 | 1 | 0 |
Anomalous Pulmonary Venous Return [description not available] | 0 | 1.93 | 1 | 0 |
Tachyarrhythmia [description not available] | 0 | 4.37 | 8 | 0 |
Paroxysmal Reciprocal Tachycardia [description not available] | 0 | 2.64 | 3 | 0 |
Tachycardia Abnormally rapid heartbeat, usually with a HEART RATE above 100 beats per minute for adults. Tachycardia accompanied by disturbance in the cardiac depolarization (cardiac arrhythmia) is called tachyarrhythmia. | 0 | 4.37 | 8 | 0 |
Tachycardia, Paroxysmal Abnormally rapid heartbeats with sudden onset and cessation. | 0 | 2.64 | 3 | 0 |
Tachycardia, Supraventricular A generic expression for any tachycardia that originates above the BUNDLE OF HIS. | 0 | 2.35 | 2 | 0 |
Astasia-Abasia [description not available] | 0 | 3.03 | 5 | 0 |
Tuberculoma A tumor-like mass resulting from the enlargement of a tuberculous lesion. | 0 | 8.33 | 7 | 0 |
Briquet Syndrome [description not available] | 0 | 2.84 | 4 | 0 |
Somatoform Disorders Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by another medical condition, by the direct effects of a substance, or by another mental disorder. The MEDICALLY UNEXPLAINED SYMPTOMS must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to FACTITIOUS DISORDERS and MALINGERING, the physical symptoms are not under voluntary control. (APA, DSM-V) | 0 | 2.84 | 4 | 0 |
Addiction, Opioid [description not available] | 0 | 2.84 | 4 | 0 |
Opioid-Related Disorders Disorders related to or resulting from abuse or misuse of OPIOIDS. | 0 | 2.84 | 4 | 0 |
Adenoma, Chromophobe A benign tumor of the anterior pituitary in which the cells do not stain with acidic or basic dyes. | 0 | 3.03 | 5 | 0 |
Angiomatosis Oculoorbital-Thalamic Syndrome [description not available] | 0 | 3.55 | 9 | 0 |
Sturge-Weber Syndrome A non-inherited congenital condition with vascular and neurological abnormalities. It is characterized by facial vascular nevi (PORT-WINE STAIN), and capillary angiomatosis of intracranial membranes (MENINGES; CHOROID). Neurological features include EPILEPSY; cognitive deficits; GLAUCOMA; and visual defects. | 0 | 3.55 | 9 | 0 |
Neuromuscular Blockade The intentional interruption of transmission at the NEUROMUSCULAR JUNCTION by external agents, usually neuromuscular blocking agents. It is distinguished from NERVE BLOCK in which nerve conduction (NEURAL CONDUCTION) is interrupted rather than neuromuscular transmission. Neuromuscular blockade is commonly used to produce MUSCLE RELAXATION as an adjunct to anesthesia during surgery and other medical procedures. It is also often used as an experimental manipulation in basic research. It is not strictly speaking anesthesia but is grouped here with anesthetic techniques. The failure of neuromuscular transmission as a result of pathological processes is not included here. | 0 | 2.85 | 4 | 0 |
Purpura, Thrombopenic [description not available] | 0 | 3.03 | 5 | 0 |
Purpura, Thrombocytopenic Any form of purpura in which the PLATELET COUNT is decreased. Many forms are thought to be caused by immunological mechanisms. | 0 | 3.03 | 5 | 0 |
Chondrodystrophic Myotonia [description not available] | 0 | 2.63 | 3 | 0 |
Leukemia, Lymphocytic [description not available] | 0 | 4.74 | 12 | 0 |
Leukemia, Lymphoid Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts. | 0 | 4.74 | 12 | 0 |
Narcosis A state of depressed CENTRAL NERVOUS SYSTEM marked by stupor or insensibility. | 0 | 8.03 | 5 | 0 |
Hypothermia, Accidental [description not available] | 0 | 3.44 | 8 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 3.44 | 8 | 0 |
Nephrolithiasis Formation of stones in the KIDNEY. | 0 | 6.93 | 1 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 1.93 | 1 | 0 |
Kidney Stones [description not available] | 0 | 2.35 | 2 | 0 |
Kidney Calculi Stones in the KIDNEY, usually formed in the urine-collecting area of the kidney (KIDNEY PELVIS). Their sizes vary and most contains CALCIUM OXALATE. | 0 | 2.35 | 2 | 0 |
Aortic Arch Syndrome [description not available] | 0 | 3.45 | 8 | 0 |
Bradykinesia [description not available] | 0 | 1.93 | 1 | 0 |
Jaw Diseases Diseases involving the JAW. | 0 | 1.93 | 1 | 0 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 2.62 | 3 | 0 |
ENT Diseases [description not available] | 0 | 2.34 | 2 | 0 |
Clasp-Knife Spasticity [description not available] | 0 | 2.34 | 2 | 0 |
Muscle Spasticity A form of muscle hypertonia associated with upper MOTOR NEURON DISEASE. Resistance to passive stretch of a spastic muscle results in minimal initial resistance (a free interval) followed by an incremental increase in muscle tone. Tone increases in proportion to the velocity of stretch. Spasticity is usually accompanied by HYPERREFLEXIA and variable degrees of MUSCLE WEAKNESS. (From Adams et al., Principles of Neurology, 6th ed, p54) | 0 | 2.34 | 2 | 0 |
Dominant Hereditary Sensory Neuropathy, Type III [description not available] | 0 | 4.94 | 9 | 0 |
Dysautonomia, Familial An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension (HYPOTENSION, ORTHOSTATIC), fixed pupils, excessive SWEATING, loss of pain and temperature sensation, and absent reflexes. Pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons. (From Adams et al., Principles of Neurology, 6th ed, p1348; Nat Genet 1993;4(2):160-4) | 0 | 4.94 | 9 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 2.33 | 2 | 0 |
Mastoiditis Inflammation of the honeycomb-like MASTOID BONE in the skull just behind the ear. It is usually a complication of OTITIS MEDIA. | 0 | 1.93 | 1 | 0 |
Pellagra A disease due to deficiency of NIACIN, a B-complex vitamin, or its precursor TRYPTOPHAN. It is characterized by scaly DERMATITIS which is often associated with DIARRHEA and DEMENTIA (the three D's). | 0 | 2.84 | 4 | 0 |
Enlarged Spleen [description not available] | 0 | 2.64 | 3 | 0 |
Chondromatosis Multiple formation of chondromas. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Cervix Diseases [description not available] | 0 | 1.93 | 1 | 0 |
Burkholderia pseudomallei Infection [description not available] | 0 | 1.93 | 1 | 0 |
Clostridium tetani Infection [description not available] | 0 | 2.62 | 3 | 0 |
Tetanus A disease caused by tetanospasmin, a powerful protein toxin produced by CLOSTRIDIUM TETANI. Tetanus usually occurs after an acute injury, such as a puncture wound or laceration. Generalized tetanus, the most common form, is characterized by tetanic muscular contractions and hyperreflexia. Localized tetanus presents itself as a mild condition with manifestations restricted to muscles near the wound. It may progress to the generalized form. | 0 | 2.62 | 3 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 1.93 | 1 | 0 |
Oligodendroglioma A relatively slow-growing glioma that is derived from oligodendrocytes and tends to occur in the cerebral hemispheres, thalamus, or lateral ventricle. They may present at any age, but are most frequent in the third to fifth decades, with an earlier incidence peak in the first decade. Histologically, these tumors are encapsulated, relatively avascular, and tend to form cysts and microcalcifications. Neoplastic cells tend to have small round nuclei surrounded by unstained nuclei. The tumors may vary from well-differentiated to highly anaplastic forms. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2052; Adams et al., Principles of Neurology, 6th ed, p655) | 0 | 1.93 | 1 | 0 |
Lymphatic Vessel Tumors Neoplasms composed of lymphoid tissue, a lattice work of reticular tissue the interspaces of which contain lymphocytes. The concept does not refer to neoplasms located in lymphatic vessels. | 0 | 1.93 | 1 | 0 |
American Trypanosomiasis [description not available] | 0 | 3.33 | 7 | 0 |
Chagas Disease Infection with the protozoan parasite TRYPANOSOMA CRUZI, a form of TRYPANOSOMIASIS endemic in Central and South America. It is named after the Brazilian physician Carlos Chagas, who discovered the parasite. Infection by the parasite (positive serologic result only) is distinguished from the clinical manifestations that develop years later, such as destruction of PARASYMPATHETIC GANGLIA; CHAGAS CARDIOMYOPATHY; and dysfunction of the ESOPHAGUS or COLON. | 0 | 8.33 | 7 | 0 |
Brittle Bone Disease [description not available] | 0 | 3.2 | 6 | 0 |
Osteogenesis Imperfecta COLLAGEN DISEASES characterized by brittle, osteoporotic, and easily fractured bones. It may also present with blue sclerae, loose joints, and imperfect dentin formation. Most types are autosomal dominant and are associated with mutations in COLLAGEN TYPE I. | 0 | 3.2 | 6 | 0 |
Rachitis [description not available] | 0 | 2.62 | 3 | 0 |
Bornholm Disease [description not available] | 0 | 1.93 | 1 | 0 |
Mesothelioma A tumor derived from mesothelial tissue (peritoneum, pleura, pericardium). It appears as broad sheets of cells, with some regions containing spindle-shaped, sarcoma-like cells and other regions showing adenomatous patterns. Pleural mesotheliomas have been linked to exposure to asbestos. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Dysautonomia [description not available] | 0 | 1.93 | 1 | 0 |
Cryoglobulinemia A condition characterized by the presence of abnormal quantities of CRYOGLOBULINS in the blood. Upon cold exposure, these abnormal proteins precipitate into the microvasculature leading to restricted blood flow in the exposed areas. | 0 | 7.62 | 3 | 0 |
Toxemia A condition produced by the presence of toxins or other harmful substances in the BLOOD. | 0 | 8.03 | 5 | 0 |
Infections, Trichomonas [description not available] | 0 | 2.34 | 2 | 0 |
Trichomonas Infections Infections in birds and mammals produced by various species of Trichomonas. | 0 | 2.34 | 2 | 0 |
ARSA Deficiency [description not available] | 0 | 2.63 | 3 | 0 |
Leukodystrophy, Metachromatic An autosomal recessive metabolic disease caused by a deficiency of CEREBROSIDE-SULFATASE leading to intralysosomal accumulation of cerebroside sulfate (SULFOGLYCOSPHINGOLIPIDS) in the nervous system and other organs. Pathological features include diffuse demyelination, and metachromatically-staining granules in many cell types such as the GLIAL CELLS. There are several allelic and nonallelic forms with a variety of neurological symptoms. | 0 | 2.63 | 3 | 0 |
Autosomal Dominant Optic Atrophy [description not available] | 0 | 2.36 | 2 | 0 |
Rhinosporidiosis Chronic, localized granulomatous infection of mucocutaneous tissues, especially the NOSE, and characterized by HYPERPLASIA and the development of POLYPS. It is found in humans and other animals and is caused by the mesomycetozoean organism RHINOSPORIDIUM SEEBERI. | 0 | 2.65 | 3 | 0 |
Deficiency, Protein [description not available] | 0 | 3.19 | 6 | 0 |
Hypervitaminosis A A symptom complex resulting from ingesting excessive amounts of VITAMIN A. | 0 | 2.62 | 3 | 0 |
Classical Swine Fever An acute, highly contagious disease affecting swine of all ages and caused by the CLASSICAL SWINE FEVER VIRUS. It has a sudden onset with high morbidity and mortality. | 0 | 1.93 | 1 | 0 |
Coronary Heart Disease [description not available] | 0 | 10.36 | 10 | 0 |
Coronary Disease An imbalance between myocardial functional requirements and the capacity of the CORONARY VESSELS to supply sufficient blood flow. It is a form of MYOCARDIAL ISCHEMIA (insufficient blood supply to the heart muscle) caused by a decreased capacity of the coronary vessels. | 0 | 5.36 | 10 | 0 |
Leishmaniasis, Mucocutaneous A disease characterized by the chronic, progressive spread of lesions from New World cutaneous leishmaniasis caused by species of the L. braziliensis complex to the nasal, pharyngeal, and buccal mucosa some time after the appearance of the initial cutaneous lesion. Nasal obstruction and epistaxis are frequent presenting symptoms. | 0 | 1.93 | 1 | 0 |
Ankylosis Fixation and immobility of a joint. | 0 | 1.93 | 1 | 0 |
Amyloidosis, Hereditary [description not available] | 0 | 2.36 | 2 | 0 |
Amyloidosis, Familial Diseases in which there is a familial pattern of AMYLOIDOSIS. | 0 | 2.36 | 2 | 0 |
Alcohol Withdrawal Associated Autonomic Hyperactivity [description not available] | 0 | 2.35 | 2 | 0 |
Psychoses, Alcoholic A group of mental disorders associated with organic brain damage and caused by poisoning from alcohol. | 0 | 2.63 | 3 | 0 |
Hydrosyringomyelia [description not available] | 0 | 2.62 | 3 | 0 |
Arteriosclerosis Obliterans Common occlusive arterial disease which is caused by ATHEROSCLEROSIS. It is characterized by lesions in the innermost layer (ARTERIAL INTIMA) of arteries including the AORTA and its branches to the extremities. Risk factors include smoking, HYPERLIPIDEMIA, and HYPERTENSION. | 0 | 2.34 | 2 | 0 |
Molluscum Contagiosum A common, benign, usually self-limited viral infection of the skin and occasionally the conjunctivae by a poxvirus (MOLLUSCUM CONTAGIOSUM VIRUS). (Dorland, 27th ed) | 0 | 3.03 | 5 | 0 |
Adie Syndrome A syndrome characterized by a TONIC PUPIL that occurs in combination with decreased lower extremity reflexes. The affected pupil will respond more briskly to accommodation than to light (light-near dissociation) and is supersensitive to dilute pilocarpine eye drops, which induce pupillary constriction. Pathologic features include degeneration of the ciliary ganglion and postganglionic parasympathetic fibers that innervate the pupillary constrictor muscle. (From Adams et al., Principles of Neurology, 6th ed, p279) | 0 | 3.95 | 5 | 0 |
Myelopathy [description not available] | 0 | 3.55 | 3 | 0 |
Spinal Cord Diseases Pathologic conditions which feature SPINAL CORD damage or dysfunction, including disorders involving the meninges and perimeningeal spaces surrounding the spinal cord. Traumatic injuries, vascular diseases, infections, and inflammatory/autoimmune processes may affect the spinal cord. | 0 | 3.55 | 3 | 0 |
Hypochondriacal Neuroses [description not available] | 0 | 2.34 | 2 | 0 |
Complex Partial Epilepsy [description not available] | 0 | 1.93 | 1 | 0 |
Epilepsy, Complex Partial A disorder characterized by recurrent partial seizures marked by impairment of cognition. During the seizure the individual may experience a wide variety of psychic phenomenon including formed hallucinations, illusions, deja vu, intense emotional feelings, confusion, and spatial disorientation. Focal motor activity, sensory alterations and AUTOMATISM may also occur. Complex partial seizures often originate from foci in one or both temporal lobes. The etiology may be idiopathic (cryptogenic partial complex epilepsy) or occur as a secondary manifestation of a focal cortical lesion (symptomatic partial complex epilepsy). (From Adams et al., Principles of Neurology, 6th ed, pp317-8) | 0 | 1.93 | 1 | 0 |
Hypoascorbemia [description not available] | 0 | 2.63 | 3 | 0 |
Scurvy An acquired blood vessel disorder caused by severe deficiency of vitamin C (ASCORBIC ACID) in the diet leading to defective collagen formation in small blood vessels. Scurvy is characterized by bleeding in any tissue, weakness, ANEMIA, spongy gums, and a brawny induration of the muscles of the calves and legs. | 0 | 7.63 | 3 | 0 |
Idiopathic Inflammatory Myopathies [description not available] | 0 | 4.47 | 9 | 0 |
Myositis Inflammation of a muscle or muscle tissue. | 0 | 4.47 | 9 | 0 |
Blepharophimosis The abnormal narrowness of the palpebral fissure in the horizontal direction caused by the lateral displacement of the medial canthi of the eyelids. (Dorland, 27th ed) | 0 | 3.58 | 3 | 0 |
Anorectal Diseases [description not available] | 0 | 1.93 | 1 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 1.93 | 1 | 0 |
Female Genital Diseases [description not available] | 0 | 3.05 | 5 | 0 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 3.05 | 5 | 0 |
Bejel [description not available] | 0 | 1.93 | 1 | 0 |
Bone Cancer [description not available] | 0 | 2.87 | 4 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 2.87 | 4 | 0 |
Central Nervous System Cysts Congenital or acquired cysts of the brain, spinal cord, or meninges which may remain stable in size or undergo progressive enlargement. | 0 | 1.93 | 1 | 0 |
Benign Paroxysmal Peritonitis [description not available] | 0 | 2.34 | 2 | 0 |
Familial Mediterranean Fever A group of HEREDITARY AUTOINFLAMMATION DISEASES, characterized by recurrent fever, abdominal pain, headache, rash, PLEURISY; and ARTHRITIS. ORCHITIS; benign MENINGITIS; and AMYLOIDOSIS may also occur. Homozygous or compound heterozygous mutations in marenostrin gene encoding PYRIN result in autosomal recessive transmission; simple heterozygous, autosomal dominant form of the disease also exists with mutations in the same gene. | 0 | 2.34 | 2 | 0 |
Beriberi A disease caused by a deficiency of thiamine (vitamin B1) and characterized by polyneuritis, cardiac pathology, and edema. The epidemic form is found primarily in areas in which white (polished) rice is the staple food, as in Japan, China, the Philippines, India, and other countries of southeast Asia. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 1.93 | 1 | 0 |
Renal Insufficiency, Chronic Conditions in which the KIDNEYS perform below the normal level for more than three months. Chronic kidney insufficiency is classified by five stages according to the decline in GLOMERULAR FILTRATION RATE and the degree of kidney damage (as measured by the level of PROTEINURIA). The most severe form is the end-stage renal disease (CHRONIC KIDNEY FAILURE). (Kidney Foundation: Kidney Disease Outcome Quality Initiative, 2002) | 0 | 1.93 | 1 | 0 |
Chondrodysplasia with Hemangioma [description not available] | 0 | 1.93 | 1 | 0 |
Entomophthoramycosis [description not available] | 0 | 2.34 | 2 | 0 |
Zygomycosis Infection in humans and animals caused by fungi in the class Zygomycetes. It includes MUCORMYCOSIS and entomophthoramycosis. The latter is a tropical infection of subcutaneous tissue or paranasal sinuses caused by fungi in the order Entomophthorales. Phycomycosis, closely related to zygomycosis, describes infection with members of Phycomycetes, an obsolete classification. | 0 | 2.34 | 2 | 0 |
Absence of Cerebral Hemispheres, Congenital [description not available] | 0 | 2.35 | 2 | 0 |
Calcium Metabolism Disorders Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization. | 0 | 2.35 | 2 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 1.93 | 1 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 1.93 | 1 | 0 |
Corpus Luteum Cyst [description not available] | 0 | 2.34 | 2 | 0 |
Ovarian Cysts General term for CYSTS and cystic diseases of the OVARY. | 0 | 2.34 | 2 | 0 |
Brain Embolism and Thrombosis [description not available] | 0 | 3.97 | 14 | 0 |
Degos Disease [description not available] | 0 | 1.93 | 1 | 0 |
Far East Scarlet-like Fever [description not available] | 0 | 1.93 | 1 | 0 |
Amino Acid Metabolism Disorders, Inborn [description not available] | 0 | 3.77 | 4 | 0 |
Hemosiderosis Conditions in which there is a generalized increase in the iron stores of body tissues, particularly of liver and the MONONUCLEAR PHAGOCYTE SYSTEM, without demonstrable tissue damage. The name refers to the presence of stainable iron in the tissue in the form of hemosiderin. | 0 | 7.87 | 4 | 0 |
Silicosis A form of pneumoconiosis resulting from inhalation of dust containing crystalline form of SILICON DIOXIDE, usually in the form of quartz. Amorphous silica is relatively nontoxic. | 0 | 7.35 | 2 | 0 |
Adhesions, Tissue [description not available] | 0 | 4.81 | 13 | 0 |
Brain Stem Neoplasms, Primary [description not available] | 0 | 1.93 | 1 | 0 |
Brain Stem Neoplasms Benign and malignant intra-axial tumors of the MESENCEPHALON; PONS; or MEDULLA OBLONGATA of the BRAIN STEM. Primary and metastatic neoplasms may occur in this location. Clinical features include ATAXIA, cranial neuropathies (see CRANIAL NERVE DISEASES), NAUSEA, hemiparesis (see HEMIPLEGIA), and quadriparesis. Primary brain stem neoplasms are more frequent in children. Histologic subtypes include GLIOMA; HEMANGIOBLASTOMA; GANGLIOGLIOMA; and EPENDYMOMA. | 0 | 1.93 | 1 | 0 |
Bilirubin Encephalopathy [description not available] | 0 | 4.24 | 4 | 0 |
Kernicterus A term used pathologically to describe BILIRUBIN staining of the BASAL GANGLIA; BRAIN STEM; and CEREBELLUM and clinically to describe a syndrome associated with HYPERBILIRUBINEMIA. Clinical features include athetosis, MUSCLE SPASTICITY or hypotonia, impaired vertical gaze, and DEAFNESS. Nonconjugated bilirubin enters the brain and acts as a neurotoxin, often in association with conditions that impair the BLOOD-BRAIN BARRIER (e.g., SEPSIS). This condition occurs primarily in neonates (INFANT, NEWBORN), but may rarely occur in adults. (Menkes, Textbook of Child Neurology, 5th ed, p613) | 0 | 4.24 | 4 | 0 |
Glossoptosis, Micrognathia, and Cleft Palate [description not available] | 0 | 1.93 | 1 | 0 |
Periarthritis Inflammation of the tissues around a joint. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Mandibular Neoplasms Tumors or cancer of the MANDIBLE. | 0 | 3.73 | 2 | 1 |
Blood Protein Disorders Hematologic diseases caused by structural or functional defects of BLOOD PROTEINS. | 0 | 2.63 | 3 | 0 |
Schwartzman Phenomenon [description not available] | 0 | 2.63 | 3 | 0 |
Actinic Keratosis [description not available] | 0 | 1.93 | 1 | 0 |
Keratoderma Blennorrhagicum [description not available] | 0 | 3.2 | 6 | 0 |
Keratosis Any horny growth such as a wart or callus. | 0 | 3.2 | 6 | 0 |
Keratosis, Actinic White or pink lesions on the arms, hands, face, or scalp that arise from sun-induced DNA DAMAGE to KERATINOCYTES in exposed areas. They are considered precursor lesions to superficial SQUAMOUS CELL CARCINOMA. | 0 | 1.93 | 1 | 0 |
Corynebacterium Infections Infections with bacteria of the genus CORYNEBACTERIUM. | 0 | 1.93 | 1 | 0 |
Hyalinosis Cutis et Mucosae [description not available] | 0 | 2.63 | 3 | 0 |
Atypical Lipoma [description not available] | 0 | 3.07 | 5 | 0 |
Lipoma A benign tumor composed of fat cells (ADIPOCYTES). It can be surrounded by a thin layer of connective tissue (encapsulated), or diffuse without the capsule. | 0 | 8.07 | 5 | 0 |
Furrow Keratitis [description not available] | 0 | 9.87 | 93 | 1 |
Hairy Cell Leukemia [description not available] | 0 | 2.63 | 3 | 0 |
Leukemia, Hairy Cell A neoplastic disease of the lymphoreticular cells which is considered to be a rare type of chronic leukemia; it is characterized by an insidious onset, splenomegaly, anemia, granulocytopenia, thrombocytopenia, little or no lymphadenopathy, and the presence of hairy or flagellated cells in the blood and bone marrow. | 0 | 2.63 | 3 | 0 |
Eye Manifestations Ocular disorders attendant upon non-ocular disease or injury. | 0 | 8.05 | 128 | 0 |
Amelia [description not available] | 0 | 1.93 | 1 | 0 |
Carcinoma 256, Walker A transplantable carcinoma of the rat that originally appeared spontaneously in the mammary gland of a pregnant albino rat, and which now resembles a carcinoma in young transplants and a sarcoma in older transplants. (Stedman, 25th ed) | 0 | 1.93 | 1 | 0 |
Apolipoprotein B-100, Familial Defective [description not available] | 0 | 3.21 | 6 | 0 |
Hyperlipoproteinemia Type II A group of familial disorders characterized by elevated circulating cholesterol contained in either LOW-DENSITY LIPOPROTEINS alone or also in VERY-LOW-DENSITY LIPOPROTEINS (pre-beta lipoproteins). | 0 | 3.21 | 6 | 0 |
Abdominal Cryptorchidism [description not available] | 0 | 2.86 | 4 | 0 |
alpha-Galactosidase A Deficiency [description not available] | 0 | 4.26 | 7 | 0 |
Angiokeratoma A vascular, horny neoplasm of the skin characterized by TELANGIECTASIS and secondary epithelial changes including acanthosis and hyperkeratosis. | 0 | 3.04 | 5 | 0 |
Fabry Disease An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. | 0 | 4.26 | 7 | 0 |
Spider Veins [description not available] | 0 | 3.45 | 8 | 0 |
Congenital Poikiloderma [description not available] | 0 | 1.93 | 1 | 0 |
Telangiectasis Permanent dilation of preexisting blood vessels (CAPILLARIES; ARTERIOLES; VENULES) creating small focal red lesions, most commonly in the skin or mucous membranes. It is characterized by the prominence of skin blood vessels, such as vascular spiders. | 0 | 3.45 | 8 | 0 |
Adenovirus Infections [description not available] | 0 | 5.02 | 16 | 0 |
Adenoviridae Infections Virus diseases caused by the ADENOVIRIDAE. | 0 | 5.02 | 16 | 0 |
Cancer of Pharynx [description not available] | 0 | 2.63 | 3 | 0 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 0 | 2.63 | 3 | 0 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 1.93 | 1 | 0 |
Cervical Fusion Syndrome [description not available] | 0 | 1.93 | 1 | 0 |
Atrial Septal Defect [description not available] | 0 | 1.93 | 1 | 0 |
Lower Extremity Deformities, Congenital Congenital structural abnormalities of the LOWER EXTREMITY. | 0 | 1.93 | 1 | 0 |
Upper Extremity Deformities, Congenital Congenital structural abnormalities of the UPPER EXTREMITY. | 0 | 1.93 | 1 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 2.36 | 2 | 0 |
Infection, Puerperal [description not available] | 0 | 1.93 | 1 | 0 |
Lupus Erythematosus, Chronic Cutaneous [description not available] | 0 | 2.63 | 3 | 0 |
Lupus Erythematosus, Discoid A chronic form of cutaneous lupus erythematosus (LUPUS ERYTHEMATOSUS, CUTANEOUS) in which the skin lesions mimic those of the systemic form but in which systemic signs are rare. It is characterized by the presence of discoid skin plaques showing varying degrees of edema, erythema, scaliness, follicular plugging, and skin atrophy. Lesions are surrounded by an elevated erythematous border. The condition typically involves the face and scalp, but widespread dissemination may occur. | 0 | 2.63 | 3 | 0 |
Congenital Familial Lymphedema [description not available] | 0 | 3.79 | 4 | 0 |
Lymphedema Edema due to obstruction of lymph vessels or disorders of the lymph nodes. | 0 | 3.79 | 4 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 4.95 | 15 | 0 |
Cerebral Arteriosclerosis [description not available] | 0 | 2.65 | 3 | 0 |
Intracranial Arteriosclerosis Vascular diseases characterized by thickening and hardening of the walls of ARTERIES inside the SKULL. There are three subtypes: (1) atherosclerosis with fatty deposits in the ARTERIAL INTIMA; (2) Monckeberg's sclerosis with calcium deposits in the media and (3) arteriolosclerosis involving the small caliber arteries. Clinical signs include HEADACHE; CONFUSION; transient blindness (AMAUROSIS FUGAX); speech impairment; and HEMIPARESIS. | 0 | 2.65 | 3 | 0 |
Pleurisy INFLAMMATION of PLEURA, the lining of the LUNG. When PARIETAL PLEURA is involved, there is pleuritic CHEST PAIN. | 0 | 1.93 | 1 | 0 |
Pediculosis [description not available] | 0 | 1.93 | 1 | 0 |
Lice Infestations Parasitic attack or subsistence on the skin by members of the order Phthiraptera, especially on humans by Pediculus humanus of the family Pediculidae. The hair of the head, eyelashes, and pubis is a frequent site of infestation. (From Dorland, 28th ed; Stedman, 26th ed) | 0 | 1.93 | 1 | 0 |
Ear Deformities, Acquired Distortion or disfigurement of the ear caused by disease or injury after birth. | 0 | 2.85 | 4 | 0 |
Teratogenesis The formation of CONGENITAL ABNORMALITIES. | 0 | 1.93 | 1 | 0 |
Acquired Nasal Deformities [description not available] | 0 | 3.33 | 7 | 0 |
Aminoaciduria, Renal [description not available] | 0 | 3.04 | 5 | 0 |
CKD-MBD [description not available] | 0 | 1.93 | 1 | 0 |
Chronic Kidney Disease-Mineral and Bone Disorder Decalcification of bone or abnormal bone development due to chronic KIDNEY DISEASES, in which 1,25-DIHYDROXYVITAMIN D3 synthesis by the kidneys is impaired, leading to reduced negative feedback on PARATHYROID HORMONE. The resulting SECONDARY HYPERPARATHYROIDISM eventually leads to bone disorders. | 0 | 1.93 | 1 | 0 |
Abscess, Pulmonary [description not available] | 0 | 2.63 | 3 | 0 |
Lung Abscess Solitary or multiple collections of PUS within the lung parenchyma as a result of infection by bacteria, protozoa, or other agents. | 0 | 2.63 | 3 | 0 |
Decerebrate Posturing [description not available] | 0 | 2.87 | 4 | 0 |
Tendinitis Inflammation of TENDONS. It is characterized by the degeneration of tendons accompanied by an inflammatory repair response, fibroblastic proliferation, and formation of granulation tissue. Tendinitis is not a clinical diagnosis and can be confirmed only by histopathological findings. | 0 | 2.37 | 2 | 0 |
Tendinopathy Clinical syndrome describing overuse tendon injuries characterized by a combination of PAIN, diffuse or localized swelling, and impaired performance. | 0 | 2.37 | 2 | 0 |
Cystadenoma A benign neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. In some instances, considerable portions of the neoplasm, or even the entire mass, may be cystic. (Stedman, 25th ed) | 0 | 2.34 | 2 | 0 |
Arcus Corneae [description not available] | 0 | 2.63 | 3 | 0 |
Larva Migrans, Visceral A condition produced in man by the prolonged migration of animal nematode larvae in extraintestinal tissues other than skin; characterized by persistent hypereosinophilia, hepatomegaly, and frequently pneumonitis, commonly caused by Toxocara canis and Toxocara cati. | 0 | 3.27 | 2 | 0 |
Amebiasis, Intestinal [description not available] | 0 | 1.94 | 1 | 0 |
Athetoid Movements [description not available] | 0 | 1.94 | 1 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 2.36 | 2 | 0 |
Anemias, Iron-Deficiency [description not available] | 0 | 2.37 | 2 | 0 |
Anemia, Iron-Deficiency Anemia characterized by decreased or absent iron stores, low serum iron concentration, low transferrin saturation, and low hemoglobin concentration or hematocrit value. The erythrocytes are hypochromic and microcytic and the iron binding capacity is increased. | 0 | 2.37 | 2 | 0 |
Bartholin-Patau Syndrome [description not available] | 0 | 2.34 | 2 | 0 |
Cardiac Septal Defect [description not available] | 0 | 1.94 | 1 | 0 |
Kwashiorkor A syndrome produced by severe protein deficiency, characterized by retarded growth, changes in skin and hair pigment, edema, and pathologic changes in the liver, including fatty infiltration, necrosis, and fibrosis. The word is a local name in Gold Coast, Africa, meaning displaced child. Although first reported from Africa, kwashiorkor is now known throughout the world, but mainly in the tropics and subtropics. It is considered to be related to marasmus. (From Dorland, 27th ed) | 0 | 2.34 | 2 | 0 |
Chondroblastoma A usually benign tumor composed of cells which arise from chondroblasts or their precursors and which tend to differentiate into cartilage cells. It occurs primarily in the epiphyses of adolescents. It is relatively rare and represents less than 2% of all primary bone tumors. The peak incidence is in the second decade of life; it is about twice as common in males as in females. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1846) | 0 | 1.94 | 1 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 3.28 | 2 | 0 |
Experimental Mammary Neoplasms [description not available] | 0 | 1.94 | 1 | 0 |
Hirsutism A condition observed in WOMEN and CHILDREN when there is excess coarse body hair of an adult male distribution pattern, such as facial and chest areas. It is the result of elevated ANDROGENS from the OVARIES, the ADRENAL GLANDS, or exogenous sources. The concept does not include HYPERTRICHOSIS, which is an androgen-independent excessive hair growth. | 0 | 2.36 | 2 | 0 |
Hypertrichosis Excessive hair growth at inappropriate locations, such as on the extremities, the head, and the back. It is caused by genetic or acquired factors, and is an androgen-independent process. This concept does not include HIRSUTISM which is an androgen-dependent excess hair growth in WOMEN and CHILDREN. | 0 | 2.36 | 2 | 0 |
Brachmann-De Lange Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Hand Deformities Alterations or deviations from normal shape or size which result in a disfigurement of the hand. | 0 | 1.94 | 1 | 0 |
De Lange Syndrome A syndrome characterized by growth retardation, severe MENTAL RETARDATION, short stature, a low-pitched growling cry, brachycephaly, low-set ears, webbed neck, carp mouth, depressed nasal bridge, bushy eyebrows meeting at the midline, hirsutism, and malformations of the hands. The condition may occur sporadically or be associated with an autosomal dominant pattern of inheritance or duplication of the long arm of chromosome 3. (Menkes, Textbook of Child Neurology, 5th ed, p231) | 0 | 1.94 | 1 | 0 |
Ascariasis Infection by nematodes of the genus ASCARIS. Ingestion of infective eggs causes diarrhea and pneumonitis. Its distribution is more prevalent in areas of poor sanitation and where human feces are used for fertilizer. | 0 | 5.53 | 17 | 0 |
Cardiac Tamponade Compression of the heart by accumulated fluid (PERICARDIAL EFFUSION) or blood (HEMOPERICARDIUM) in the PERICARDIUM surrounding the heart. The affected cardiac functions and CARDIAC OUTPUT can range from minimal to total hemodynamic collapse. | 0 | 1.94 | 1 | 0 |
Hemoperitoneum Accumulations of blood in the PERITONEAL CAVITY due to internal HEMORRHAGE. | 0 | 1.94 | 1 | 0 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 2.35 | 2 | 0 |
Gastric Ulcer [description not available] | 0 | 2.66 | 3 | 0 |
Stomach Ulcer Ulceration of the GASTRIC MUCOSA due to contact with GASTRIC JUICE. It is often associated with HELICOBACTER PYLORI infection or consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 2.66 | 3 | 0 |
A-V Dissociation [description not available] | 0 | 2.63 | 3 | 0 |
Sex Disorders [description not available] | 0 | 1.94 | 1 | 0 |
Sexual Dysfunction, Physiological Physiological disturbances in normal sexual performance in either the male or the female. | 0 | 1.94 | 1 | 0 |
Cogan Syndrome A condition consisting of inflammatory eye disease usually presenting as interstitial KERATITIS, vestibuloauditory dysfunction, and large- to medium-vessel vasculitis. | 0 | 1.94 | 1 | 0 |
Deficiency, Ascorbic Acid [description not available] | 0 | 3.55 | 3 | 0 |
Ascorbic Acid Deficiency A condition due to a dietary deficiency of ascorbic acid (vitamin C), characterized by malaise, lethargy, and weakness. As the disease progresses, joints, muscles, and subcutaneous tissues may become the sites of hemorrhage. Ascorbic acid deficiency frequently develops into SCURVY in young children fed unsupplemented cow's milk exclusively during their first year. It develops also commonly in chronic alcoholism. (Cecil Textbook of Medicine, 19th ed, p1177) | 0 | 3.55 | 3 | 0 |
Entropion The turning inward (inversion) of the edge of the eyelid, with the tarsal cartilage turned inward toward the eyeball. (Dorland, 27th ed) | 0 | 3.27 | 2 | 0 |
ARC [description not available] | 0 | 1.94 | 1 | 0 |
AIDS-Related Complex A prodromal phase of infection with the human immunodeficiency virus (HIV). Laboratory criteria separating AIDS-related complex (ARC) from AIDS include elevated or hyperactive B-cell humoral immune responses, compared to depressed or normal antibody reactivity in AIDS; follicular or mixed hyperplasia in ARC lymph nodes, leading to lymphocyte degeneration and depletion more typical of AIDS; evolving succession of histopathological lesions such as localization of Kaposi's sarcoma, signaling the transition to the full-blown AIDS. | 0 | 1.94 | 1 | 0 |
Acrodynia A condition seen primarily in childhood, most often resulting from chronic exposure to MERCURY COMPOUNDS which may result in encephalopathy and POLYNEUROPATHY. Clinical features include pain, swelling and pinkish discoloration of the fingers and toes, weakness in the extremities, extreme irritability, HYPERESTHESIA, and alterations in level of consciousness. (From Menkes, Textbook of Child Neurology, 5th ed, p603) | 0 | 1.94 | 1 | 0 |
Cystadenoma, Papillary A benign neoplasm of the ovary. | 0 | 1.94 | 1 | 0 |
Lung Diseases, Parasitic Infections of the lungs with parasites, most commonly by parasitic worms (HELMINTHS). | 0 | 2.36 | 2 | 0 |
Classic Galactosemia [description not available] | 0 | 2.64 | 3 | 0 |
Galactosemias A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3) | 0 | 2.64 | 3 | 0 |
Algodystrophic Syndrome [description not available] | 0 | 2.34 | 2 | 0 |
Reflex Sympathetic Dystrophy A syndrome characterized by severe burning pain in an extremity accompanied by sudomotor, vasomotor, and trophic changes in bone without an associated specific nerve injury. This condition is most often precipitated by trauma to soft tissue or nerve complexes. The skin over the affected region is usually erythematous and demonstrates hypersensitivity to tactile stimuli and erythema. (Adams et al., Principles of Neurology, 6th ed, p1360; Pain 1995 Oct;63(1):127-33) | 0 | 2.34 | 2 | 0 |
Serum Sickness Immune complex disease caused by the administration of foreign serum or serum proteins and characterized by fever, lymphadenopathy, arthralgia, and urticaria. When they are complexed to protein carriers, some drugs can also cause serum sickness when they act as haptens inducing antibody responses. | 0 | 1.93 | 1 | 0 |
Batten Turner Congenital Myopathy [description not available] | 0 | 1.93 | 1 | 0 |
Paragonimiasis Infection with TREMATODA of the genus PARAGONIMUS. | 0 | 1.93 | 1 | 0 |
Enterobiasis Infection with nematodes of the genus ENTEROBIUS; E. vermicularis, the pinworm of man, causes a crawling sensation and pruritus. This condition results in scratching the area, occasionally causing scarification. | 0 | 1.93 | 1 | 0 |
Aspiculariasis [description not available] | 0 | 1.93 | 1 | 0 |
Prurigo A name applied to several itchy skin eruptions of unknown cause. The characteristic course is the formation of a dome-shaped papule with a small transient vesicle on top, followed by crusting over or lichenification. (From Dorland, 27th ed) | 0 | 2.36 | 2 | 0 |
Hemoglobin C Disease A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice. | 0 | 2.34 | 2 | 0 |
Cholesteatoma A non-neoplastic mass of keratin-producing squamous EPITHELIUM, frequently occurring in the MENINGES; bones of the skull, and most commonly in the MIDDLE EAR and MASTOID region. Cholesteatoma can be congenital or acquired. Cholesteatoma is not a tumor nor is it associated with high CHOLESTEROL. | 0 | 2.34 | 2 | 0 |
Hepatitis, Infectious [description not available] | 0 | 1.93 | 1 | 0 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 2.63 | 3 | 0 |
Hepatitis A INFLAMMATION of the LIVER in humans caused by a member of the HEPATOVIRUS genus, HUMAN HEPATITIS A VIRUS. It can be transmitted through fecal contamination of food or water. | 0 | 1.93 | 1 | 0 |
Hemorrhagic Fevers, Viral A group of viral diseases of diverse etiology but having many similar clinical characteristics; increased capillary permeability, leukopenia, and thrombocytopenia are common to all. Hemorrhagic fevers are characterized by sudden onset, fever, headache, generalized myalgia, backache, conjunctivitis, and severe prostration, followed by various hemorrhagic symptoms. Hemorrhagic fever with kidney involvement is HEMORRHAGIC FEVER WITH RENAL SYNDROME. | 0 | 1.93 | 1 | 0 |
Basal Ganglia Diseases Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA. | 0 | 3.78 | 4 | 0 |
Dysentery Acute inflammation of the intestine associated with infectious DIARRHEA of various etiologies, generally acquired by eating contaminated food containing TOXINS, BIOLOGICAL derived from BACTERIA or other microorganisms. Dysentery is characterized initially by watery FECES then by bloody mucoid stools. It is often associated with ABDOMINAL PAIN; FEVER; and DEHYDRATION. | 0 | 1.93 | 1 | 0 |
Carotid Arteriopathies, Traumatic [description not available] | 0 | 2.87 | 4 | 0 |
Carcinomatous Meningitis [description not available] | 0 | 1.93 | 1 | 0 |
Meningeal Carcinomatosis Primary or secondary neoplasm in the ARACHNOID or SUBARACHNOID SPACE. It appears as a diffuse fibrotic thickening of the MENINGES associated with variable degrees of inflammation. | 0 | 1.93 | 1 | 0 |
Acquired Gerstmann Syndrome [description not available] | 0 | 1.93 | 1 | 0 |
Hiccough [description not available] | 0 | 1.93 | 1 | 0 |
Acute Q Fever [description not available] | 0 | 1.93 | 1 | 0 |
Chromosomal Breakage [description not available] | 0 | 2.41 | 2 | 0 |
Emesis, Postoperative [description not available] | 0 | 4.72 | 2 | 1 |
Postoperative Nausea and Vomiting Emesis and queasiness occurring after anesthesia. | 0 | 4.72 | 2 | 1 |
Starvation Lengthy and continuous deprivation of food. (Stedman, 25th ed) | 0 | 2.35 | 2 | 0 |
Mycosis Fungoides A chronic, malignant T-cell lymphoma of the skin. In the late stages, the LYMPH NODES and viscera are affected. | 0 | 7.85 | 4 | 0 |
Dental Focal Infection [description not available] | 0 | 2.62 | 3 | 0 |
Beryllium Disease Disease resulting from exposure to beryllium. Entry into the body is not limited to the inhalation route. | 0 | 1.92 | 1 | 0 |
Berylliosis A form of pneumoconiosis caused by inhaled rare metal BERYLLIUM or its soluble salts which are used in a wide variety of industry including alloys, ceramics, radiographic equipment, and vacuum tubes. Berylliosis is characterized by an acute inflammatory reaction in the upper airway leading to BRONCHIOLITIS; PULMONARY EDEMA; and pneumonia. | 0 | 1.92 | 1 | 0 |
Paralysis, Legs [description not available] | 0 | 2.35 | 2 | 0 |
Paraplegia Severe or complete loss of motor function in the lower extremities and lower portions of the trunk. This condition is most often associated with SPINAL CORD DISEASES, although BRAIN DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; NEUROMUSCULAR DISEASES; and MUSCULAR DISEASES may also cause bilateral leg weakness. | 0 | 7.35 | 2 | 0 |
Congenital Oculofacial Paralysis, Moebius [description not available] | 0 | 1.92 | 1 | 0 |
Jaundice, Spirochetal [description not available] | 0 | 3.55 | 3 | 0 |
Circulatory Collapse [description not available] | 0 | 3.96 | 5 | 0 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 3.96 | 5 | 0 |
Hives [description not available] | 0 | 3.55 | 3 | 0 |
Urticaria A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress. | 0 | 3.55 | 3 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 4.6 | 6 | 0 |
Leukocyte Disorders Disordered formation of various types of leukocytes or an abnormal accumulation or deficiency of these cells. | 0 | 1.92 | 1 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 4.6 | 6 | 0 |
Cacosmia [description not available] | 0 | 4.46 | 5 | 1 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 1.92 | 1 | 0 |
Meningitis, Viral Viral infections of the leptomeninges and subarachnoid space. TOGAVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; RUBELLA; BUNYAVIRIDAE INFECTIONS; ORBIVIRUS infections; PICORNAVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RHABDOVIRIDAE INFECTIONS; ARENAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; JC VIRUS infections; and RETROVIRIDAE INFECTIONS may cause this form of meningitis. Clinical manifestations include fever, headache, neck pain, vomiting, PHOTOPHOBIA, and signs of meningeal irritation. (From Joynt, Clinical Neurology, 1996, Ch26, pp1-3) | 0 | 2.64 | 3 | 0 |
Carbamoyl Phosphate Synthase (Ammonia) Deficiency Disease [description not available] | 0 | 1.92 | 1 | 0 |
Carbamoyl-Phosphate Synthase I Deficiency Disease A urea cycle disorder manifesting in infancy as lethargy, emesis, seizures, alterations of muscle tone, abnormal eye movements, and an elevation of serum ammonia. The disorder is caused by a reduction in the activity of hepatic mitochondrial CARBAMOYL-PHOSPHATE SYNTHASE (AMMONIA). (Menkes, Textbook of Child Neurology, 5th ed, pp50-1) | 0 | 1.92 | 1 | 0 |
Angiohemophilia [description not available] | 0 | 1.92 | 1 | 0 |
von Willebrand Diseases Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. | 0 | 1.92 | 1 | 0 |
Biliary Cirrhosis [description not available] | 0 | 2.34 | 2 | 0 |
Liver Cirrhosis, Biliary FIBROSIS of the hepatic parenchyma due to obstruction of BILE flow (CHOLESTASIS) in the intrahepatic or extrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC; BILE DUCTS, EXTRAHEPATIC). Primary biliary cholangitis involves the destruction of small intra-hepatic bile ducts and decreased bile secretion. Secondary biliary cholangitis is produced by prolonged obstruction of large intrahepatic or extrahepatic bile ducts from a variety of causes. | 0 | 2.34 | 2 | 0 |
Paranoia [description not available] | 0 | 3.77 | 4 | 0 |
Dental Diseases [description not available] | 0 | 2.36 | 2 | 0 |
Helminthiasis, Animal Infestation of animals with parasitic worms of the helminth class. The infestation may be experimental or veterinary. | 0 | 2.71 | 3 | 0 |
Bites [description not available] | 0 | 2.36 | 2 | 0 |
Ambiguous Genitalia [description not available] | 0 | 2.67 | 3 | 0 |
Disorders of Sex Development In gonochoristic organisms, congenital conditions in which development of chromosomal, gonadal, or anatomical sex is atypical. Effects from exposure to abnormal levels of GONADAL HORMONES in the maternal environment, or disruption of the function of those hormones by ENDOCRINE DISRUPTORS are included. | 0 | 2.67 | 3 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 3.07 | 5 | 0 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 2.68 | 3 | 0 |
Hepatitis B INFLAMMATION of the LIVER in humans caused by a member of the ORTHOHEPADNAVIRUS genus, HEPATITIS B VIRUS. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 3.07 | 5 | 0 |
Hepatitis C INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown. | 0 | 7.68 | 3 | 0 |
Aspergillosis, Nervous System Invasive [description not available] | 0 | 2.02 | 1 | 0 |
Neuroaspergillosis Infections of the nervous system caused by fungi of the genus ASPERGILLUS, most commonly ASPERGILLUS FUMIGATUS. Aspergillus infections may occur in immunocompetent hosts, but are more prevalent in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES. The organism may spread to the nervous system from focal infections in the lung, mastoid region, sinuses, inner ear, bones, eyes, gastrointestinal tract, and heart. Sinus infections may be locally invasive and enter the intracranial compartment, producing MENINGITIS, FUNGAL; cranial neuropathies; and abscesses in the frontal lobes of the brain. (From Joynt, Clinical Neurology, 1998, Ch 27, pp62-3) | 0 | 2.02 | 1 | 0 |
Argentaffinoma [description not available] | 0 | 3.32 | 2 | 0 |
Cancer of Rectum [description not available] | 0 | 2.02 | 1 | 0 |
Carcinoid Tumor A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182) | 0 | 3.32 | 2 | 0 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 2.02 | 1 | 0 |
Orthopedic Disorders [description not available] | 0 | 2.93 | 1 | 0 |
Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | 0 | 2.93 | 1 | 0 |
Bulbar Palsy [description not available] | 0 | 2.02 | 1 | 0 |
Interstitial Nephritis [description not available] | 0 | 2.93 | 1 | 0 |
Nephritis, Interstitial Inflammation of the interstitial tissue of the kidney. This term is generally used for primary inflammation of KIDNEY TUBULES and/or surrounding interstitium. For primary inflammation of glomerular interstitium, see GLOMERULONEPHRITIS. Infiltration of the inflammatory cells into the interstitial compartment results in EDEMA, increased spaces between the tubules, and tubular renal dysfunction. | 0 | 2.93 | 1 | 0 |
As If Personality [description not available] | 0 | 1.92 | 1 | 0 |
Central Diabetes Insipidus [description not available] | 0 | 1.92 | 1 | 0 |
Diabetes Insipidus A disease that is characterized by frequent urination, excretion of large amounts of dilute URINE, and excessive THIRST. Etiologies of diabetes insipidus include deficiency of antidiuretic hormone (also known as ADH or VASOPRESSIN) secreted by the NEUROHYPOPHYSIS, impaired KIDNEY response to ADH, and impaired hypothalamic regulation of thirst. | 0 | 2.34 | 2 | 0 |
Diabetes Insipidus, Neurogenic A genetic or acquired polyuric disorder caused by a deficiency of VASOPRESSINS secreted by the NEUROHYPOPHYSIS. Clinical signs include the excretion of large volumes of dilute URINE; HYPERNATREMIA; THIRST; and polydipsia. Etiologies include HEAD TRAUMA; surgeries and diseases involving the HYPOTHALAMUS and the PITUITARY GLAND. This disorder may also be caused by mutations of genes such as ARVP encoding vasopressin and its corresponding neurophysin (NEUROPHYSINS). | 0 | 1.92 | 1 | 0 |
Anemia, Macrocytic Anemia characterized by larger than normal erythrocytes, increased mean corpuscular volume (MCV) and increased mean corpuscular hemoglobin (MCH). | 0 | 1.92 | 1 | 0 |
Alogia [description not available] | 0 | 2.84 | 4 | 0 |
Aphasia A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia. | 0 | 7.84 | 4 | 0 |
Myxedema A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLYSACCHARIDES in the SKIN and other tissues. It is caused by a deficiency of THYROID HORMONES. The skin becomes puffy around the eyes and on the cheeks. The face is dull and expressionless with thickened nose and lips. | 0 | 6.92 | 1 | 0 |
Paratyphoid Fever A prolonged febrile illness commonly caused by several Paratyphi serotypes of SALMONELLA ENTERICA. It is similar to TYPHOID FEVER but less severe. | 0 | 2.33 | 2 | 0 |
Macrocephaly [description not available] | 0 | 1.92 | 1 | 0 |
Acute Necrotizing Encephalitis, Herpetic [description not available] | 0 | 2.35 | 2 | 0 |
Encephalitis, Herpes Simplex An acute (or rarely chronic) inflammatory process of the brain caused by SIMPLEXVIRUS infections which may be fatal. The majority of infections are caused by human herpesvirus 1 (HERPESVIRUS 1, HUMAN) and less often by human herpesvirus 2 (HERPESVIRUS 2, HUMAN). Clinical manifestations include FEVER; HEADACHE; SEIZURES; HALLUCINATIONS; behavioral alterations; APHASIA; hemiparesis; and COMA. Pathologically, the condition is marked by a hemorrhagic necrosis involving the medial and inferior TEMPORAL LOBE and orbital regions of the FRONTAL LOBE. (From Adams et al., Principles of Neurology, 6th ed, pp751-4) | 0 | 2.35 | 2 | 0 |
Chlamydia pneumoniae Infections [description not available] | 0 | 2.02 | 1 | 0 |
Sterility, Female [description not available] | 0 | 2.69 | 3 | 0 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 2.69 | 3 | 0 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 2.02 | 1 | 0 |
Chemical Sensitivities, Multiple [description not available] | 0 | 4.09 | 3 | 1 |
Bronchial Hyperreactivity Tendency of the smooth muscle of the tracheobronchial tree to contract more intensely in response to a given stimulus than it does in the response seen in normal individuals. This condition is present in virtually all symptomatic patients with asthma. The most prominent manifestation of this smooth muscle contraction is a decrease in airway caliber that can be readily measured in the pulmonary function laboratory. | 0 | 3.8 | 2 | 1 |
Cancer of Mouth [description not available] | 0 | 5.01 | 5 | 2 |
Mandibular Diseases Diseases involving the MANDIBLE. | 0 | 3.77 | 2 | 1 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 5.01 | 5 | 2 |
Osteoradionecrosis Necrosis of bone following radiation injury. | 0 | 4.37 | 2 | 2 |
Brain Ventricular Neoplasms [description not available] | 0 | 2.02 | 1 | 0 |
Rhabdoid Tumor A rare but highly lethal childhood tumor found almost exclusively in infants. Histopathologically, it resembles RHABDOMYOSARCOMA but the tumor cells are not of myogenic origin. Although it arises primarily in the kidney, it may be found in other parts of the body. The rhabdoid cytomorphology is believed to be the expression of a very primitive malignant cell. (From Holland et al., Cancer Medicine, 3d ed, p2210) | 0 | 7.02 | 1 | 0 |
Prosthesis Durability [description not available] | 0 | 3.62 | 3 | 0 |
EBV Infections [description not available] | 0 | 2.42 | 2 | 0 |
Epstein-Barr Virus Infections Infection with human herpesvirus 4 (HERPESVIRUS 4, HUMAN); which may facilitate the development of various lymphoproliferative disorders. These include BURKITT LYMPHOMA (African type), INFECTIOUS MONONUCLEOSIS, and oral hairy leukoplakia (LEUKOPLAKIA, HAIRY). | 0 | 2.42 | 2 | 0 |
Wallerian Degeneration Degeneration of distal aspects of a nerve axon following injury to the cell body or proximal portion of the axon. The process is characterized by fragmentation of the axon and its MYELIN SHEATH. | 0 | 2.67 | 3 | 0 |
Infections, Tick-Borne [description not available] | 0 | 2.02 | 1 | 0 |
Malignancies, Post-Traumatic [description not available] | 0 | 2.02 | 1 | 0 |
Benign Frontal Childhood Epilepsy [description not available] | 0 | 2.02 | 1 | 0 |
AIRE Deficiency [description not available] | 0 | 2.7 | 3 | 0 |
Sensation Disorders Disorders of the special senses (i.e., VISION; HEARING; TASTE; and SMELL) or somatosensory system (i.e., afferent components of the PERIPHERAL NERVOUS SYSTEM). | 0 | 5.22 | 4 | 1 |
Infections, Morbillivirus [description not available] | 0 | 2.02 | 1 | 0 |
Femoral Fractures Fractures of the femur. | 0 | 2.02 | 1 | 0 |
Spinal Stenosis Narrowing of the spinal canal. | 0 | 2.94 | 4 | 0 |
Diffuse Cutaneous Systemic Sclerosis [description not available] | 0 | 2.03 | 1 | 0 |
Scleroderma, Diffuse A rapid onset form of SYSTEMIC SCLERODERMA with progressive widespread SKIN thickening over the arms, the legs and the trunk, resulting in stiffness and disability. | 0 | 2.03 | 1 | 0 |
Psoriasis Arthropathica [description not available] | 0 | 2.4 | 2 | 0 |
Arthritis, Psoriatic A type of inflammatory arthritis associated with PSORIASIS, often involving the axial joints and the peripheral terminal interphalangeal joints. It is characterized by the presence of HLA-B27-associated SPONDYLARTHROPATHY, and the absence of rheumatoid factor. | 0 | 2.4 | 2 | 0 |
Caliciviridae Infections Virus diseases caused by CALICIVIRIDAE. They include HEPATITIS E; VESICULAR EXANTHEMA OF SWINE; acute respiratory infections in felines, rabbit hemorrhagic disease, and some cases of gastroenteritis in humans. | 0 | 2.03 | 1 | 0 |
Abnormalities, Sex Chromosome [description not available] | 0 | 2.87 | 4 | 0 |
Dermatitis, Radiation-Induced [description not available] | 0 | 4.6 | 4 | 0 |
Radiodermatitis A cutaneous inflammatory reaction occurring as a result of exposure to ionizing radiation. | 0 | 4.6 | 4 | 0 |
Lupus Vulgaris A form of cutaneous tuberculosis. It is seen predominantly in women and typically involves the NASAL MUCOSA; BUCCAL MUCOSA; and conjunctival mucosa. | 0 | 2.33 | 2 | 0 |
Anoxia-Ischemia, Brain [description not available] | 0 | 2.03 | 1 | 0 |
Hypoxia-Ischemia, Brain A disorder characterized by a reduction of oxygen in the blood combined with reduced blood flow (ISCHEMIA) to the brain from a localized obstruction of a cerebral artery or from systemic hypoperfusion. Prolonged hypoxia-ischemia is associated with ISCHEMIC ATTACK, TRANSIENT; BRAIN INFARCTION; BRAIN EDEMA; COMA; and other conditions. | 0 | 2.03 | 1 | 0 |
Enterovirus Infections Diseases caused by ENTEROVIRUS. | 0 | 2.39 | 2 | 0 |
Communicable Diseases, Emerging Infectious diseases that are novel in their outbreak ranges (geographic and host) or transmission mode. | 0 | 2.03 | 1 | 0 |
Acute Kidney Failure [description not available] | 0 | 3.22 | 6 | 0 |
Acute Kidney Injury Abrupt reduction in kidney function. Acute kidney injury encompasses the entire spectrum of the syndrome including acute kidney failure; ACUTE KIDNEY TUBULAR NECROSIS; and other less severe conditions. | 0 | 3.22 | 6 | 0 |
Dermatitis, Periocular [description not available] | 0 | 2.03 | 1 | 0 |
Dermatitis, Perioral A papular eruption of unknown etiology that progresses to residual papular erythema and scaling usually confined to the area of the mouth, and almost exclusively occurring in young women. It may also be localized or extend to involve the eyelids and adjacent glabella area of the forehead (periocular dermatitis). (Dorland, 28th ed) | 0 | 2.03 | 1 | 0 |
Angor Pectoris [description not available] | 0 | 4.06 | 3 | 0 |
Angina Pectoris The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION. | 0 | 4.06 | 3 | 0 |
Urethritis Inflammation involving the URETHRA. Similar to CYSTITIS, clinical symptoms range from vague discomfort to painful urination (DYSURIA), urethral discharge, or both. | 0 | 2.03 | 1 | 0 |
Developmental Coordination Disorder [description not available] | 0 | 4.1 | 3 | 1 |
Drop Attack [description not available] | 0 | 3.36 | 7 | 0 |
Syncope A transient loss of consciousness and postural tone caused by diminished blood flow to the brain (i.e., BRAIN ISCHEMIA). Presyncope refers to the sensation of lightheadedness and loss of strength that precedes a syncopal event or accompanies an incomplete syncope. (From Adams et al., Principles of Neurology, 6th ed, pp367-9) | 0 | 8.36 | 7 | 0 |
Absence Seizure Disorder [description not available] | 0 | 2.39 | 2 | 0 |
Epilepsy, Absence A seizure disorder usually occurring in childhood characterized by rhythmic electrical brain discharges of generalized onset. Clinical features include a sudden cessation of ongoing activity usually without loss of postural tone. Rhythmic blinking of the eyelids or lip smacking frequently accompanies the SEIZURES. The usual duration is 5-10 seconds, and multiple episodes may occur daily. Juvenile absence epilepsy is characterized by the juvenile onset of absence seizures and an increased incidence of myoclonus and tonic-clonic seizures. (Menkes, Textbook of Child Neurology, 5th ed, p736) | 0 | 2.39 | 2 | 0 |
Choline Deficiency A condition produced by a deficiency of CHOLINE in animals. Choline is known as a lipotropic agent because it has been shown to promote the transport of excess fat from the liver under certain conditions in laboratory animals. Combined deficiency of choline (included in the B vitamin complex) and all other methyl group donors causes liver cirrhosis in some animals. Unlike compounds normally considered as vitamins, choline does not serve as a cofactor in enzymatic reactions. (From Saunders Dictionary & Encyclopedia of Laboratory Medicine and Technology, 1984) | 0 | 2.03 | 1 | 0 |
Acute Kidney Tubular Necrosis [description not available] | 0 | 2.03 | 1 | 0 |
Glomerular Necrosis [description not available] | 0 | 2.38 | 2 | 0 |
Kidney Tubular Necrosis, Acute Acute kidney failure resulting from destruction of EPITHELIAL CELLS of the KIDNEY TUBULES. It is commonly attributed to exposure to toxic agents or renal ISCHEMIA following severe TRAUMA. | 0 | 2.03 | 1 | 0 |
Abnormalities, Teeth [description not available] | 0 | 3.06 | 5 | 0 |
Deficiency, Folic Acid [description not available] | 0 | 2.65 | 3 | 0 |
Deficiency, Vitamin B 12 [description not available] | 0 | 2.88 | 4 | 0 |
Folic Acid Deficiency A nutritional condition produced by a deficiency of FOLIC ACID in the diet. Many plant and animal tissues contain folic acid, abundant in green leafy vegetables, yeast, liver, and mushrooms but destroyed by long-term cooking. Alcohol interferes with its intermediate metabolism and absorption. Folic acid deficiency may develop in long-term anticonvulsant therapy or with use of oral contraceptives. This deficiency causes anemia, macrocytic anemia, and megaloblastic anemia. It is indistinguishable from vitamin B 12 deficiency in peripheral blood and bone marrow findings, but the neurologic lesions seen in B 12 deficiency do not occur. (Merck Manual, 16th ed) | 0 | 2.65 | 3 | 0 |
Vitamin B 12 Deficiency A nutritional condition produced by a deficiency of VITAMIN B 12 in the diet, characterized by megaloblastic anemia. Since vitamin B 12 is not present in plants, humans have obtained their supply from animal products, from multivitamin supplements in the form of pills, and as additives to food preparations. A wide variety of neuropsychiatric abnormalities is also seen in vitamin B 12 deficiency and appears to be due to an undefined defect involving myelin synthesis. (From Cecil Textbook of Medicine, 19th ed, p848) | 0 | 2.88 | 4 | 0 |
Sick Building Syndrome A group of symptoms that are two- to three-fold more common in those who work in large, energy-efficient buildings, associated with an increased frequency of headaches, lethargy, and dry skin. Clinical manifestations include hypersensitivity pneumonitis (ALVEOLITIS, EXTRINSIC ALLERGIC); allergic rhinitis (RHINITIS, ALLERGIC, PERENNIAL); ASTHMA; infections, skin eruptions, and mucous membrane irritation syndromes. Current usage tends to be less restrictive with regard to the type of building and delineation of complaints. (From Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.42 | 2 | 0 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 3.57 | 3 | 0 |
Chemical and Drug Induced Liver Injury A spectrum of clinical liver diseases ranging from mild biochemical abnormalities to ACUTE LIVER FAILURE, caused by drugs, drug metabolites, herbal and dietary supplements and chemicals from the environment. | 0 | 3.57 | 3 | 0 |
Ape Diseases Diseases of chimpanzees, gorillas, and orangutans. | 0 | 2.02 | 1 | 0 |
Alcohol Abuse, Nervous System [description not available] | 0 | 2.03 | 1 | 0 |
Back Ache [description not available] | 0 | 2.03 | 1 | 0 |
Lordosis The anterior concavity in the curvature of the lumbar and cervical spine as viewed from the side. The term usually refers to abnormally increased curvature (hollow back, saddle back, swayback). It does not include lordosis as normal mating posture in certain animals ( = POSTURE + SEX BEHAVIOR, ANIMAL). | 0 | 2.03 | 1 | 0 |
Back Pain Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions. | 0 | 2.03 | 1 | 0 |
Abnormalities, Radiation-Induced Congenital changes in the morphology of organs produced by exposure to ionizing or non-ionizing radiation. | 0 | 4.15 | 6 | 0 |
Coxsackie Virus Infections [description not available] | 0 | 2.38 | 2 | 0 |
Colitis Inflammation of the COLON section of the large intestine (INTESTINE, LARGE), usually with symptoms such as DIARRHEA (often with blood and mucus), ABDOMINAL PAIN, and FEVER. | 0 | 2.95 | 1 | 0 |
Anorexia The lack or loss of APPETITE accompanied by an aversion to food and the inability to eat. It is the defining characteristic of the disorder ANOREXIA NERVOSA. | 0 | 4.28 | 4 | 1 |
Apnea, Central [description not available] | 0 | 2.03 | 1 | 0 |
Flushing A transient reddening of the face that may be due to fever, certain drugs, exertion, or stress. | 0 | 2.03 | 1 | 0 |
Sleep Apnea, Central A condition associated with multiple episodes of sleep apnea which are distinguished from obstructive sleep apnea (SLEEP APNEA, OBSTRUCTIVE) by the complete cessation of efforts to breathe. This disorder is associated with dysfunction of central nervous system centers that regulate respiration. | 0 | 2.03 | 1 | 0 |
Pulsatile Tinnitus [description not available] | 0 | 2.03 | 1 | 0 |
Tinnitus A nonspecific symptom of hearing disorder characterized by the sensation of buzzing, ringing, clicking, pulsations, and other noises in the ear. Objective tinnitus refers to noises generated from within the ear or adjacent structures that can be heard by other individuals. The term subjective tinnitus is used when the sound is audible only to the affected individual. Tinnitus may occur as a manifestation of COCHLEAR DISEASES; VESTIBULOCOCHLEAR NERVE DISEASES; INTRACRANIAL HYPERTENSION; CRANIOCEREBRAL TRAUMA; and other conditions. | 0 | 2.03 | 1 | 0 |
Nasal Polyps Focal accumulations of EDEMA fluid in the NASAL MUCOSA accompanied by HYPERPLASIA of the associated submucosal connective tissue. Polyps may be NEOPLASMS, foci of INFLAMMATION, degenerative lesions, or malformations. | 0 | 2.03 | 1 | 0 |
Infectious Bovine Rhinotracheitis A herpesvirus infection of CATTLE characterized by INFLAMMATION and NECROSIS of the mucous membranes of the upper RESPIRATORY TRACT. | 0 | 3.36 | 7 | 0 |
Epiglottitis Inflammation of the EPIGLOTTIS. | 0 | 2.03 | 1 | 0 |
Ureteral Diseases Pathological processes involving the URETERS. | 0 | 3.42 | 1 | 1 |
Carotid Artery Dissection, Internal [description not available] | 0 | 2.04 | 1 | 0 |
Congenital X-Linked Retinoschisis [description not available] | 0 | 2.05 | 1 | 0 |
Encephalitis Lethargica Type Parkinsonism [description not available] | 0 | 1.92 | 1 | 0 |
Parkinson Disease, Postencephalitic Parkinsonism following encephalitis, historically seen as a sequella of encephalitis lethargica (Von Economo Encephalitis). The early age of onset, the rapid progression of symptoms followed by stabilization, and the presence of a variety of other neurological disorders (e.g., sociopathic behavior; TICS; MUSCLE SPASMS; oculogyric crises; hyperphagia; and bizarre movements) distinguish this condition from primary PARKINSON DISEASE. Pathologic features include neuronal loss and gliosis concentrated in the MESENCEPHALON; SUBTHALAMUS; and HYPOTHALAMUS. (From Adams et al., Principles of Neurology, 6th ed, p754) | 0 | 1.92 | 1 | 0 |
Insulin Coma Severe HYPOGLYCEMIA induced by a large dose of exogenous INSULIN resulting in a COMA or profound state of unconsciousness from which the individual cannot be aroused. | 0 | 1.92 | 1 | 0 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 3.55 | 3 | 0 |
Ectoparasitic Infestations Infestations by PARASITES which live on, or burrow into, the surface of their host's EPIDERMIS. Most ectoparasites are ARTHROPODS. | 0 | 2.86 | 4 | 0 |
Hyperdactyly [description not available] | 0 | 2.04 | 1 | 0 |
Mucopolysaccharidosis [description not available] | 0 | 4.82 | 13 | 0 |
Gargoylism, Hunter Syndrome [description not available] | 0 | 2.38 | 2 | 0 |
Mucopolysaccharidoses Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency. | 0 | 4.82 | 13 | 0 |
Mucopolysaccharidosis II Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15. | 0 | 2.38 | 2 | 0 |
Adjustment Disorder [description not available] | 0 | 2.05 | 1 | 0 |
Adjustment Disorders Maladaptive reactions to identifiable psychosocial stressors occurring within a short time after onset of the stressor. They are manifested by either impairment in social or occupational functioning or by symptoms (depression, anxiety, etc.) that are in excess of a normal and expected reaction to the stressor. | 0 | 2.05 | 1 | 0 |
Injuries, Maxillofacial [description not available] | 0 | 4.46 | 5 | 0 |
Fibroma, Shope [description not available] | 0 | 2.7 | 3 | 0 |
Cramp [description not available] | 0 | 2.34 | 2 | 0 |
Muscle Cramp A sustained and usually painful contraction of muscle fibers. This may occur as an isolated phenomenon or as a manifestation of an underlying disease process (e.g., UREMIA; HYPOTHYROIDISM; MOTOR NEURON DISEASE; etc.). (From Adams et al., Principles of Neurology, 6th ed, p1398) | 0 | 2.34 | 2 | 0 |
Patency of the Ductus Arteriosus [description not available] | 0 | 1.94 | 1 | 0 |
Ductus Arteriosus, Patent A congenital heart defect characterized by the persistent opening of fetal DUCTUS ARTERIOSUS that connects the PULMONARY ARTERY to the descending aorta (AORTA, DESCENDING) allowing unoxygenated blood to bypass the lung and flow to the PLACENTA. Normally, the ductus is closed shortly after birth. | 0 | 1.94 | 1 | 0 |
Experimental Leukemia [description not available] | 0 | 2.36 | 2 | 0 |
Hypertension, Renal Persistent high BLOOD PRESSURE due to KIDNEY DISEASES, such as those involving the renal parenchyma, the renal vasculature, or tumors that secrete RENIN. | 0 | 1.94 | 1 | 0 |
Urinary Tract Infections Inflammatory responses of the epithelium of the URINARY TRACT to microbial invasions. They are often bacterial infections with associated BACTERIURIA and PYURIA. | 0 | 3.27 | 2 | 0 |
Dyskinesia, Medication-Induced [description not available] | 0 | 5.42 | 3 | 1 |
Dyskinesia, Drug-Induced Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of the face, trunk, neck, and extremities are most commonly affected. Tardive dyskinesia refers to abnormal hyperkinetic movements of the muscles of the face, tongue, and neck associated with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS). (Adams et al., Principles of Neurology, 6th ed, p1199) | 0 | 5.42 | 3 | 1 |
Benign Cranial Nerve Neoplasms [description not available] | 0 | 3.57 | 3 | 0 |
Agricultural Worker Disease [description not available] | 0 | 3.05 | 5 | 0 |
Pregnancy in Diabetes [description not available] | 0 | 3.74 | 2 | 0 |
Bilateral Wilms Tumor [description not available] | 0 | 3.98 | 5 | 0 |
Wilms Tumor A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN. | 0 | 3.98 | 5 | 0 |
Agranulocytosis, Feline [description not available] | 0 | 2.87 | 1 | 0 |
Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiency [description not available] | 0 | 2.65 | 3 | 0 |
Mucopolysaccharidosis III Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme. | 0 | 2.65 | 3 | 0 |
Canine Infectious Hepatitis [description not available] | 0 | 1.96 | 1 | 0 |
Esophageal Varices [description not available] | 0 | 1.96 | 1 | 0 |
Esophageal and Gastric Varices Dilated blood vessels in the ESOPHAGUS or GASTRIC FUNDUS that shunt blood from the portal circulation (PORTAL SYSTEM) to the systemic venous circulation. Often they are observed in individuals with portal hypertension (HYPERTENSION, PORTAL). | 0 | 1.96 | 1 | 0 |
Infections, Spirochaetales [description not available] | 0 | 2.88 | 1 | 0 |
Marasmus [description not available] | 0 | 2.36 | 2 | 0 |
Protein-Energy Malnutrition The lack of sufficient energy or protein to meet the body's metabolic demands, as a result of either an inadequate dietary intake of protein, intake of poor quality dietary protein, increased demands due to disease, or increased nutrient losses. | 0 | 2.36 | 2 | 0 |
Ganglioside Storage Diseases [description not available] | 0 | 3.97 | 5 | 0 |
Gangliosidoses A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway. | 0 | 3.97 | 5 | 0 |
Arthus Phenomenon [description not available] | 0 | 4.85 | 8 | 0 |
Chediak-Higashi Syndrome A form of phagocyte bactericidal dysfunction characterized by unusual oculocutaneous albinism, high incidence of lymphoreticular neoplasms, and recurrent pyogenic infections. In many cell types, abnormal lysosomes are present leading to defective pigment distribution and abnormal neutrophil functions. The disease is transmitted by autosomal recessive inheritance and a similar disorder occurs in the beige mouse, the Aleutian mink, and albino Hereford cattle. | 0 | 2.66 | 3 | 0 |
Cattle Plague [description not available] | 0 | 2.38 | 2 | 0 |
Venous Insufficiency Impaired venous blood flow or venous return (venous stasis), usually caused by inadequate venous valves. Venous insufficiency often occurs in the legs, and is associated with EDEMA and sometimes with VENOUS STASIS ULCERS at the ankle. | 0 | 2.89 | 4 | 0 |
Chronic Hepatitis [description not available] | 0 | 1.96 | 1 | 0 |
Hepatitis, Chronic INFLAMMATION of the LIVER with ongoing hepatocellular injury for 6 months or more, characterized by NECROSIS of HEPATOCYTES and inflammatory cell (LEUKOCYTES) infiltration. Chronic hepatitis can be caused by viruses, medications, autoimmune diseases, and other unknown factors. | 0 | 1.96 | 1 | 0 |
Alpha-Fucosidase Deficiency [description not available] | 0 | 2.37 | 2 | 0 |
Fucosidosis An autosomal recessive lysosomal storage disease caused by a deficiency of ALPHA-L-FUCOSIDASE activity resulting in an accumulation of fucose containing SPHINGOLIPIDS; GLYCOPROTEINS, and mucopolysaccharides (GLYCOSAMINOGLYCANS) in lysosomes. The infantile form (type I) features psychomotor deterioration, MUSCLE SPASTICITY, coarse facial features, growth retardation, skeletal abnormalities, visceromegaly, SEIZURES, recurrent infections, and MACROGLOSSIA, with death occurring in the first decade of life. Juvenile fucosidosis (type II) is the more common variant and features a slowly progressive decline in neurologic function and angiokeratoma corporis diffusum. Type II survival may be through the fourth decade of life. (From Menkes, Textbook of Child Neurology, 5th ed, p87; Am J Med Genet 1991 Jan;38(1):111-31) | 0 | 7.37 | 2 | 0 |
Bacterial Endocarditides, Subacute [description not available] | 0 | 1.96 | 1 | 0 |
Actinobacillus Infections Infections with bacteria of the genus ACTINOBACILLUS. | 0 | 1.96 | 1 | 0 |
Addison Disease and Cerebral Sclerosis [description not available] | 0 | 2.37 | 2 | 0 |
Adrenoleukodystrophy An X-linked recessive disorder characterized by the accumulation of saturated very long chain fatty acids in the LYSOSOMES of ADRENAL CORTEX and the white matter of CENTRAL NERVOUS SYSTEM. This disease occurs almost exclusively in the males. Clinical features include the childhood onset of ATAXIA; NEUROBEHAVIORAL MANIFESTATIONS; HYPERPIGMENTATION; ADRENAL INSUFFICIENCY; SEIZURES; MUSCLE SPASTICITY; and DEMENTIA. The slowly progressive adult form is called adrenomyeloneuropathy. The defective gene ABCD1 is located at Xq28, and encodes the adrenoleukodystrophy protein (ATP-BINDING CASSETTE TRANSPORTERS). | 0 | 2.37 | 2 | 0 |
Bronchospasm [description not available] | 0 | 2.64 | 3 | 0 |
Bronchial Spasm Spasmodic contraction of the smooth muscle of the bronchi. | 0 | 2.64 | 3 | 0 |
Monkey Diseases Diseases of Old World and New World monkeys. This term includes diseases of baboons but not of chimpanzees or gorillas (= APE DISEASES). | 0 | 3.56 | 9 | 0 |
Amnesia-Memory Loss [description not available] | 0 | 1.96 | 1 | 0 |
Amnesia Pathologic partial or complete loss of the ability to recall past experiences (AMNESIA, RETROGRADE) or to form new memories (AMNESIA, ANTEROGRADE). This condition may be of organic or psychologic origin. Organic forms of amnesia are usually associated with dysfunction of the DIENCEPHALON or HIPPOCAMPUS. (From Adams et al., Principles of Neurology, 6th ed, pp426-7) | 0 | 1.96 | 1 | 0 |
Carcinoma, Papillary A malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. (Stedman, 25th ed) | 0 | 3.35 | 1 | 1 |
Lip Diseases Diseases involving the LIP. | 0 | 1.96 | 1 | 0 |
Protozoan Infections, Animal Infections with unicellular organisms formerly members of the subkingdom Protozoa. The infections may be experimental or veterinary. | 0 | 3.79 | 4 | 0 |
Histomoniasis [description not available] | 0 | 2.87 | 4 | 0 |
Masochism Pleasure derived from being physically or psychologically abused, whether inflicted by oneself or by others. Masochism includes sexual masochism. | 0 | 1.96 | 1 | 0 |
Cockayne Syndrome A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is caused by mutations of a number of autosomal recessive genes encoding proteins that involve transcriptional-coupled DNA REPAIR processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms. | 0 | 3.3 | 2 | 0 |
Lymphangiectasis A transient dilatation of the lymphatic vessels. | 0 | 1.96 | 1 | 0 |
Burns, Electric Burns produced by contact with electric current or from a sudden discharge of electricity. | 0 | 2.65 | 3 | 0 |
Leukemia, Acute Monocytic [description not available] | 0 | 1.95 | 1 | 0 |
Leukemia, Monocytic, Acute An acute myeloid leukemia in which 80% or more of the leukemic cells are of monocytic lineage including monoblasts, promonocytes, and MONOCYTES. | 0 | 1.95 | 1 | 0 |
Glycogenosis [description not available] | 0 | 7.36 | 2 | 0 |
Acid Alpha-Glucosidase Deficiency [description not available] | 0 | 2.65 | 3 | 0 |
Glycogen Storage Disease A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement. | 0 | 2.36 | 2 | 0 |
Glycogen Storage Disease Type II An autosomal recessively inherited glycogen storage disease caused by GLUCAN 1,4-ALPHA-GLUCOSIDASE deficiency. Large amounts of GLYCOGEN accumulate in the LYSOSOMES of skeletal muscle (MUSCLE, SKELETAL); HEART; LIVER; SPINAL CORD; and BRAIN. Three forms have been described: infantile, childhood, and adult. The infantile form is fatal in infancy and presents with hypotonia and a hypertrophic cardiomyopathy (CARDIOMYOPATHY, HYPERTROPHIC). The childhood form usually presents in the second year of life with proximal weakness and respiratory symptoms. The adult form consists of a slowly progressive proximal myopathy. (From Muscle Nerve 1995;3:S61-9; Menkes, Textbook of Child Neurology, 5th ed, pp73-4) | 0 | 2.65 | 3 | 0 |
Haemophilus influenzae Meningitis Type B [description not available] | 0 | 2.37 | 2 | 0 |
Malignant Catarrh A herpesvirus infection of cattle characterized by catarrhal inflammation of the upper respiratory and alimentary epithelia, keratoconjunctivitis, encephalitis and lymph node enlargement. Syn: bovine epitheliosis, snotsiekte. | 0 | 3.34 | 7 | 0 |
Atherosclerotic Parkinsonism [description not available] | 0 | 4.26 | 4 | 0 |
Parkinson Disease, Secondary Conditions which feature clinical manifestations resembling primary Parkinson disease that are caused by a known or suspected condition. Examples include parkinsonism caused by vascular injury, drugs, trauma, toxin exposure, neoplasms, infections and degenerative or hereditary conditions. Clinical features may include bradykinesia, rigidity, parkinsonian gait, and masked facies. In general, tremor is less prominent in secondary parkinsonism than in the primary form. (From Joynt, Clinical Neurology, 1998, Ch38, pp39-42) | 0 | 4.26 | 4 | 0 |
Atypical Cluster Headache [description not available] | 0 | 4.27 | 7 | 0 |
Cephalgia, Vascular [description not available] | 0 | 4.66 | 11 | 0 |
Scarlet Fever Infection with group A streptococci that is characterized by tonsillitis and pharyngitis. An erythematous rash is commonly present. | 0 | 1.96 | 1 | 0 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 1.96 | 1 | 0 |
Infantile Respiratory Distress Syndrome [description not available] | 0 | 4.27 | 4 | 1 |
Disseminated Intravascular Coagulation A disorder characterized by procoagulant substances entering the general circulation causing a systemic thrombotic process. The activation of the clotting mechanism may arise from any of a number of disorders. A majority of the patients manifest skin lesions, sometimes leading to PURPURA FULMINANS. | 0 | 1.96 | 1 | 0 |
Respiratory Distress Syndrome, Newborn A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause. | 0 | 4.27 | 4 | 1 |
Carcinoma, Bronchial [description not available] | 0 | 1.96 | 1 | 0 |
Carcinoma, Bronchogenic Malignant neoplasm arising from the epithelium of the BRONCHI. It represents a large group of epithelial lung malignancies which can be divided into two clinical groups: SMALL CELL LUNG CANCER and NON-SMALL-CELL LUNG CARCINOMA. | 0 | 1.96 | 1 | 0 |
Acquired Language Disorders [description not available] | 0 | 3.27 | 2 | 0 |
Language Disorders Conditions characterized by deficiencies of comprehension or expression of written and spoken forms of language. These include acquired and developmental disorders. | 0 | 3.27 | 2 | 0 |
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans [description not available] | 0 | 1.95 | 1 | 0 |
Achondroplasia An autosomal dominant disorder that is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and mid-face hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, GENU VARUM, and trident hand. (Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim, MIM#100800, April 20, 2001) | 0 | 1.95 | 1 | 0 |
Anochlesia [description not available] | 0 | 2.35 | 2 | 0 |
Aleutian Disease of Mink [description not available] | 0 | 2.37 | 2 | 0 |
Avian Leukosis A group of transmissible viral diseases of chickens and turkeys. Liver tumors are found in most forms, but tumors can be found elsewhere. | 0 | 2.36 | 2 | 0 |
Hand Deformities, Acquired Deformities of the hand, or a part of the hand, acquired after birth as the result of injury or disease. | 0 | 1.96 | 1 | 0 |
Foot Deformities, Acquired Distortion or disfigurement of the foot, or a part of the foot, acquired through disease or injury after birth. | 0 | 1.96 | 1 | 0 |
Infections, Respirovirus [description not available] | 0 | 2.37 | 2 | 0 |
Pancytopenia Deficiency of all three cell elements of the blood, erythrocytes, leukocytes and platelets. | 0 | 1.95 | 1 | 0 |
Mediastinitis Inflammation of the mediastinum, the area between the pleural sacs. | 0 | 1.95 | 1 | 0 |
Adult Sandhoff Disease [description not available] | 0 | 1.95 | 1 | 0 |
Sandhoff Disease An autosomal recessive neurodegenerative disorder characterized by an accumulation of G(M2) GANGLIOSIDE in neurons and other tissues. It is caused by mutation in the common beta subunit of HEXOSAMINIDASE A and HEXOSAMINIDASE B. Thus this disease is also known as the O variant since both hexosaminidase A and B are missing. Clinically, it is indistinguishable from TAY-SACHS DISEASE. | 0 | 1.95 | 1 | 0 |
Craniofacial Pain Syndromes [description not available] | 0 | 5.28 | 7 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 4.76 | 5 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 4.76 | 5 | 0 |
Cancer of Lip [description not available] | 0 | 1.95 | 1 | 0 |
Leukemia L 1210 [description not available] | 0 | 1.98 | 1 | 0 |
Eisenmenger Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
Eisenmenger Complex A condition associated with VENTRICULAR SEPTAL DEFECT and other congenital heart defects that allow the mixing of pulmonary and systemic circulation, increase blood flow into the lung, and subsequent responses to low oxygen in blood. This complex is characterized by progressive PULMONARY HYPERTENSION; HYPERTROPHY of the RIGHT VENTRICLE; CYANOSIS; and ERYTHROCYTOSIS. | 0 | 1.98 | 1 | 0 |
Acquired Metabolic Diseases, Brain [description not available] | 0 | 3.3 | 2 | 0 |
Lipodystrophy, Intestinal [description not available] | 0 | 2.9 | 1 | 0 |
Craniomandibular Diseases [description not available] | 0 | 1.98 | 1 | 0 |
Acquired-Immune Deficiency Syndrome Dementia Complex [description not available] | 0 | 1.98 | 1 | 0 |
AIDS Dementia Complex A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40) | 0 | 1.98 | 1 | 0 |
Tooth Fractures Break or rupture of a tooth or tooth root. | 0 | 1.98 | 1 | 0 |
Malabsorption Syndromes General term for a group of MALNUTRITION syndromes caused by failure of normal INTESTINAL ABSORPTION of nutrients. | 0 | 1.98 | 1 | 0 |
Leprosy, Cutaneous [description not available] | 0 | 1.98 | 1 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 2.9 | 1 | 0 |
Leiomyosarcoma A sarcoma containing large spindle cells of smooth muscle. Although it rarely occurs in soft tissue, it is common in the viscera. It is the most common soft tissue sarcoma of the gastrointestinal tract and uterus. The median age of patients is 60 years. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1865) | 0 | 2.9 | 1 | 0 |
Apnea A transient absence of spontaneous respiration. | 0 | 3.06 | 5 | 0 |
Carcinoma, Ductal, Breast An invasive (infiltrating) CARCINOMA of the mammary ductal system (MAMMARY GLANDS) in the human BREAST. | 0 | 1.98 | 1 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 4.04 | 3 | 0 |
Peptic Ulcer Ulcer that occurs in the regions of the GASTROINTESTINAL TRACT which come into contact with GASTRIC JUICE containing PEPSIN and GASTRIC ACID. It occurs when there are defects in the MUCOSA barrier. The common forms of peptic ulcers are associated with HELICOBACTER PYLORI and the consumption of nonsteroidal anti-inflammatory drugs (NSAIDS). | 0 | 4.04 | 3 | 0 |
Obstructive Lung Diseases [description not available] | 0 | 3.28 | 2 | 0 |
Lung Diseases, Obstructive Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent. | 0 | 3.28 | 2 | 0 |
Granuloma Annulare Benign granulomatous disease of unknown etiology characterized by a ring of localized or disseminated papules or nodules on the skin and palisading histiocytes surrounding necrobiotic tissue resulting from altered collagen structures. | 0 | 1.98 | 1 | 0 |
Autoimmune Thyroiditis [description not available] | 0 | 2.88 | 4 | 0 |
Actinomycetoma [description not available] | 0 | 1.98 | 1 | 0 |
Mycetoma A chronic progressive subcutaneous infection caused by species of fungi (eumycetoma), or actinomycetes (actinomycetoma). It is characterized by tumefaction, abscesses, and tumor-like granules representing microcolonies of pathogens, such as MADURELLA fungi and bacteria ACTINOMYCETES, with different grain colors. | 0 | 1.98 | 1 | 0 |
Deficiency, Protein C [description not available] | 0 | 1.98 | 1 | 0 |
Infections, Lentivirus [description not available] | 0 | 2.39 | 2 | 0 |
Delusional Disorder Disorder with presentation of a facade of coldness with characteristic pervasive mistrust and suspiciousness of others. | 0 | 4.04 | 3 | 1 |
Gyrate Atrophy Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood. | 0 | 1.98 | 1 | 0 |
Benign Psychomotor Epilepsy, Childhood [description not available] | 0 | 2.36 | 2 | 0 |
Epilepsy, Temporal Lobe A localization-related (focal) form of epilepsy characterized by recurrent seizures that arise from foci within the TEMPORAL LOBE, most commonly from its mesial aspect. A wide variety of psychic phenomena may be associated, including illusions, hallucinations, dyscognitive states, and affective experiences. The majority of complex partial seizures (see EPILEPSY, COMPLEX PARTIAL) originate from the temporal lobes. Temporal lobe seizures may be classified by etiology as cryptogenic, familial, or symptomatic. (From Adams et al., Principles of Neurology, 6th ed, p321). | 0 | 2.36 | 2 | 0 |
Plasmodium falciparum Malaria [description not available] | 0 | 3.77 | 2 | 1 |
Malaria, Falciparum Malaria caused by PLASMODIUM FALCIPARUM. This is the severest form of malaria and is associated with the highest levels of parasites in the blood. This disease is characterized by irregularly recurring febrile paroxysms that in extreme cases occur with acute cerebral, renal, or gastrointestinal manifestations. | 0 | 3.77 | 2 | 1 |
MELAS [description not available] | 0 | 1.98 | 1 | 0 |
MELAS Syndrome A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117) | 0 | 1.98 | 1 | 0 |
AIDS-Associated Lymphoma [description not available] | 0 | 3.31 | 2 | 0 |
Lymphoma, AIDS-Related B-cell lymphoid tumors that occur in association with AIDS. Patients often present with an advanced stage of disease and highly malignant subtypes including BURKITT LYMPHOMA; IMMUNOBLASTIC LARGE-CELL LYMPHOMA; PRIMARY EFFUSION LYMPHOMA; and DIFFUSE, LARGE B-CELL, LYMPHOMA. The tumors are often disseminated in unusual extranodal sites and chromosomal abnormalities are frequently present. It is likely that polyclonal B-cell lymphoproliferation in AIDS is a complex result of EBV infection, HIV antigenic stimulation, and T-cell-dependent HIV activation. | 0 | 3.31 | 2 | 0 |
Infections, Retroviridae [description not available] | 0 | 1.98 | 1 | 0 |
Retroviridae Infections Virus diseases caused by the RETROVIRIDAE. | 0 | 1.98 | 1 | 0 |
Experimental Hepatoma [description not available] | 0 | 1.98 | 1 | 0 |
Renal Artery Stenosis [description not available] | 0 | 1.98 | 1 | 0 |
Renal Artery Obstruction Narrowing or occlusion of the RENAL ARTERY or arteries. It is due usually to ATHEROSCLEROSIS; FIBROMUSCULAR DYSPLASIA; THROMBOSIS; EMBOLISM, or external pressure. The reduced renal perfusion can lead to renovascular hypertension (HYPERTENSION, RENOVASCULAR). | 0 | 1.98 | 1 | 0 |
Brain Abscess A circumscribed collection of purulent exudate in the brain, due to bacterial and other infections. The majority are caused by spread of infected material from a focus of suppuration elsewhere in the body, notably the PARANASAL SINUSES, middle ear (see EAR, MIDDLE); HEART (see also ENDOCARDITIS, BACTERIAL), and LUNG. Penetrating CRANIOCEREBRAL TRAUMA and NEUROSURGICAL PROCEDURES may also be associated with this condition. Clinical manifestations include HEADACHE; SEIZURES; focal neurologic deficits; and alterations of consciousness. (Adams et al., Principles of Neurology, 6th ed, pp712-6) | 0 | 4.25 | 7 | 0 |
Carditis [description not available] | 0 | 2.39 | 2 | 0 |
Myocarditis Inflammatory processes of the muscular walls of the heart (MYOCARDIUM) which result in injury to the cardiac muscle cells (MYOCYTES, CARDIAC). Manifestations range from subclinical to sudden death (DEATH, SUDDEN). Myocarditis in association with cardiac dysfunction is classified as inflammatory CARDIOMYOPATHY usually caused by INFECTION, autoimmune diseases, or responses to toxic substances. Myocarditis is also a common cause of DILATED CARDIOMYOPATHY and other cardiomyopathies. | 0 | 2.39 | 2 | 0 |
Leprosy, Macular [description not available] | 0 | 1.98 | 1 | 0 |
Cancer of Endometrium [description not available] | 0 | 2.9 | 1 | 0 |
Endometrial Neoplasms Tumors or cancer of ENDOMETRIUM, the mucous lining of the UTERUS. These neoplasms can be benign or malignant. Their classification and grading are based on the various cell types and the percent of undifferentiated cells. | 0 | 2.9 | 1 | 0 |
Abortion, Veterinary Premature expulsion of the FETUS in animals. | 0 | 2.88 | 4 | 0 |
Bovine Virus Diarrhea Mucosal Disease [description not available] | 0 | 2.38 | 2 | 0 |
Fungemia The presence of fungi circulating in the blood. Opportunistic fungal sepsis is seen most often in immunosuppressed patients with severe neutropenia or in postoperative patients with intravenous catheters and usually follows prolonged antibiotic therapy. | 0 | 3.6 | 3 | 0 |
P carinii Infection [description not available] | 0 | 2.67 | 3 | 0 |
Pneumocystis Infections Infections with species in the genus PNEUMOCYSTIS, a fungus causing interstitial plasma cell pneumonia (PNEUMONIA, PNEUMOCYSTIS) and other infections in humans and other MAMMALS. Immunocompromised patients, especially those with AIDS, are particularly susceptible to these infections. Extrapulmonary sites are rare but seen occasionally. | 0 | 2.67 | 3 | 0 |
Fungal Lung Diseases [description not available] | 0 | 3.28 | 2 | 0 |
Ascaridida Infections Infections with nematodes of the order ASCARIDIDA. | 0 | 1.99 | 1 | 0 |
Liver Diseases, Parasitic Liver diseases caused by infections with PARASITES, such as tapeworms (CESTODA) and flukes (TREMATODA). | 0 | 1.99 | 1 | 0 |
Labor, Premature [description not available] | 0 | 1.99 | 1 | 0 |
AIDS Wasting Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
HIV Wasting Syndrome Involuntary weight loss of greater than 10 percent associated with intermittent or constant fever and chronic diarrhea or fatigue for more than 30 days in the absence of a defined cause other than HIV infection. A constant feature is major muscle wasting with scattered myofiber degeneration. A variety of etiologies, which vary among patients, contributes to this syndrome. (From Harrison's Principles of Internal Medicine, 13th ed, p1611). | 0 | 1.99 | 1 | 0 |
Amyloid Neuropathies Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349) | 0 | 2.39 | 2 | 0 |
Left Ventricular Hypertrophy [description not available] | 0 | 1.99 | 1 | 0 |
Hypertrophy, Left Ventricular Enlargement of the LEFT VENTRICLE of the heart. This increase in ventricular mass is attributed to sustained abnormal pressure or volume loads and is a contributor to cardiovascular morbidity and mortality. | 0 | 1.99 | 1 | 0 |
Maxillary Neoplasms Cancer or tumors of the MAXILLA or upper jaw. | 0 | 2.37 | 2 | 0 |
Ameloblastoma An immature epithelial tumor of the JAW originating from the epithelial rests of Malassez or from other epithelial remnants of the ENAMEL from the developmental period. It is a slowly growing tumor, usually benign, but displays a marked propensity for invasive growth. | 0 | 1.99 | 1 | 0 |
Bladder Disorder, Neurogenic [description not available] | 0 | 2.9 | 1 | 0 |
Urinary Bladder, Neurogenic Dysfunction of the URINARY BLADDER due to disease of the central or peripheral nervous system pathways involved in the control of URINATION. This is often associated with SPINAL CORD DISEASES, but may also be caused by BRAIN DISEASES or PERIPHERAL NERVE DISEASES. | 0 | 2.9 | 1 | 0 |
Besnoitiasis [description not available] | 0 | 2.39 | 2 | 0 |
Abnormalities, Urogenital [description not available] | 0 | 3.3 | 2 | 0 |
Alagille Syndrome 1 [description not available] | 0 | 2.68 | 3 | 0 |
Alagille Syndrome A multisystem disorder that is characterized by aplasia of intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC), and malformations in the cardiovascular system, the eyes, the vertebral column, and the facies. Major clinical features include JAUNDICE, and congenital heart disease with peripheral PULMONARY STENOSIS. Alagille syndrome may result from heterogeneous gene mutations, including mutations in JAG1 on CHROMOSOME 20 (Type 1) and NOTCH2 on CHROMOSOME 1 (Type 2). | 0 | 2.68 | 3 | 0 |
Cerebral Malaria [description not available] | 0 | 2.4 | 2 | 0 |
Entrapment Neuropathies [description not available] | 0 | 2.66 | 3 | 0 |
Ventricular Dysfunction A condition in which HEART VENTRICLES exhibit impaired function. | 0 | 1.99 | 1 | 0 |
Neurally Mediated Faint [description not available] | 0 | 1.99 | 1 | 0 |
Cherubism A fibro-osseous hereditary disease of the jaws. The swollen jaws and raised eyes give a cherubic appearance; multiple radiolucencies are evident upon radiographic examination. | 0 | 1.99 | 1 | 0 |
Intestinal Diseases, Parasitic Infections of the INTESTINES with PARASITES, commonly involving PARASITIC WORMS. Infections with roundworms (NEMATODE INFECTIONS) and tapeworms (CESTODE INFECTIONS) are also known as HELMINTHIASIS. | 0 | 2.66 | 3 | 0 |
Astroblastoma [description not available] | 0 | 1.99 | 1 | 0 |
Neoplasms, Neuroepithelial Neoplasms composed of neuroepithelial cells, which have the capacity to differentiate into NEURONS, oligodendrocytes, and ASTROCYTES. The majority of craniospinal tumors are of neuroepithelial origin. (From Dev Biol 1998 Aug 1;200(1):1-5) | 0 | 1.99 | 1 | 0 |
Fibroadenoma An adenoma containing fibrous tissue. It should be differentiated from ADENOFIBROMA which is a tumor composed of connective tissue (fibroma) containing glandular (adeno-) structures. (From Dorland, 27th ed) | 0 | 1.99 | 1 | 0 |
Cancer of Testis [description not available] | 0 | 1.99 | 1 | 0 |
Cancer Syndromes, Hereditary [description not available] | 0 | 1.99 | 1 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 1.99 | 1 | 0 |
Cervix Dysplasia [description not available] | 0 | 1.99 | 1 | 0 |
Uterine Cervical Dysplasia Abnormal development of immature squamous EPITHELIAL CELLS of the UTERINE CERVIX, a term used to describe premalignant cytological changes in the cervical EPITHELIUM. These atypical cells do not penetrate the epithelial BASEMENT MEMBRANE. | 0 | 1.99 | 1 | 0 |
Alveolar Proteinoses, Pulmonary [description not available] | 0 | 1.99 | 1 | 0 |
Pulmonary Alveolar Proteinosis A PULMONARY ALVEOLI-filling disease, characterized by dense phospholipoproteinaceous deposits in the alveoli, cough, and DYSPNEA. This disease is often related to, congenital or acquired, impaired processing of PULMONARY SURFACTANTS by alveolar macrophages, a process dependent on GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR. | 0 | 1.99 | 1 | 0 |
B-K Mole Syndrome [description not available] | 0 | 2.91 | 1 | 0 |
Dysplastic Nevus Syndrome Clinically atypical nevi (usually exceeding 5 mm in diameter and having variable pigmentation and ill defined borders) with an increased risk for development of non-familial cutaneous malignant melanoma. Biopsies show melanocytic dysplasia. Nevi are clinically and histologically identical to the precursor lesions for melanoma in the B-K mole syndrome. (Stedman, 25th ed) | 0 | 2.91 | 1 | 0 |
Cutaneous T-Cell Lymphoma [description not available] | 0 | 2.91 | 1 | 0 |
Lymphoma, T-Cell, Cutaneous A group of lymphomas exhibiting clonal expansion of malignant T-lymphocytes arrested at varying stages of differentiation as well as malignant infiltration of the skin. MYCOSIS FUNGOIDES; SEZARY SYNDROME; LYMPHOMATOID PAPULOSIS; and PRIMARY CUTANEOUS ANAPLASTIC LARGE CELL LYMPHOMA are the best characterized of these disorders. | 0 | 2.91 | 1 | 0 |
Air Sickness [description not available] | 0 | 5.97 | 4 | 1 |
Motion Sickness Disorder caused by motion. It includes sea sickness, train sickness, roller coaster rides, rocking chair, hammock swing, car sickness, air sickness, or SPACE MOTION SICKNESS. Symptoms include nausea, vomiting and/or dizziness. | 0 | 5.97 | 4 | 1 |
Labhart-Willi Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
Prader-Willi Syndrome An autosomal dominant disorder caused by deletion of the proximal long arm of the paternal chromosome 15 (15q11-q13) or by inheritance of both of the pair of chromosomes 15 from the mother (UNIPARENTAL DISOMY) which are imprinted (GENETIC IMPRINTING) and hence silenced. Clinical manifestations include MENTAL RETARDATION; MUSCULAR HYPOTONIA; HYPERPHAGIA; OBESITY; short stature; HYPOGONADISM; STRABISMUS; and HYPERSOMNOLENCE. (Menkes, Textbook of Child Neurology, 5th ed, p229) | 0 | 1.99 | 1 | 0 |
Albright Hereditary Osteodystrophy [description not available] | 0 | 1.99 | 1 | 0 |
Pseudohypoparathyroidism A hereditary syndrome clinically similar to HYPOPARATHYROIDISM. It is characterized by HYPOCALCEMIA; HYPERPHOSPHATEMIA; and associated skeletal development impairment and caused by failure of response to PARATHYROID HORMONE rather than deficiencies. A severe form with resistance to multiple hormones is referred to as Type 1a and is associated with maternal mutant allele of the ALPHA CHAIN OF STIMULATORY G PROTEIN. | 0 | 1.99 | 1 | 0 |
Focal Segmental Glomerulosclerosis [description not available] | 0 | 3.3 | 2 | 0 |
Leiomyomatosis The state of having multiple leiomyomas throughout the body. (Stedman, 25th ed) | 0 | 2.91 | 1 | 0 |
Glomerulosclerosis, Focal Segmental A clinicopathological syndrome or diagnostic term for a type of glomerular injury that has multiple causes, primary or secondary. Clinical features include PROTEINURIA, reduced GLOMERULAR FILTRATION RATE, and EDEMA. Kidney biopsy initially indicates focal segmental glomerular consolidation (hyalinosis) or scarring which can progress to globally sclerotic glomeruli leading to eventual KIDNEY FAILURE. | 0 | 3.3 | 2 | 0 |
Factitious Disorders Disorders characterized by physical or psychological symptoms that are not real, genuine, or natural. | 0 | 2.4 | 2 | 0 |
Battered Child Syndrome A clinical condition resulting from repeated physical and psychological injuries inflicted on a child by the parents or caregivers. | 0 | 1.99 | 1 | 0 |
Hepatic Failure [description not available] | 0 | 2 | 1 | 0 |
Liver Failure Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed) | 0 | 2 | 1 | 0 |
Anaplasma Infection [description not available] | 0 | 2 | 1 | 0 |
Corridor Disease [description not available] | 0 | 2 | 1 | 0 |
Central Nervous System Viral Diseases Viral infections of the brain, spinal cord, meninges, or perimeningeal spaces. | 0 | 2 | 1 | 0 |
Keloid A sharply elevated, irregularly shaped, progressively enlarging scar resulting from formation of excessive amounts of collagen in the dermis during connective tissue repair. It is differentiated from a hypertrophic scar (CICATRIX, HYPERTROPHIC) in that the former does not spread to surrounding tissues. | 0 | 2 | 1 | 0 |
Teratocarcinoma A malignant neoplasm consisting of elements of teratoma with those of embryonal carcinoma or choriocarcinoma, or both. It occurs most often in the testis. (Dorland, 27th ed) | 0 | 2 | 1 | 0 |
Granulocytic Leukemia, Chronic, Stable Phase [description not available] | 0 | 2 | 1 | 0 |
Cardiac Hypertrophy Enlargement of the HEART due to chamber HYPERTROPHY, an increase in wall thickness without an increase in the number of cells (MYOCYTES, CARDIAC). It is the result of increase in myocyte size, mitochondrial and myofibrillar mass, as well as changes in extracellular matrix. | 0 | 2 | 1 | 0 |
Cardiomegaly Enlargement of the HEART, usually indicated by a cardiothoracic ratio above 0.50. Heart enlargement may involve the right, the left, or both HEART VENTRICLES or HEART ATRIA. Cardiomegaly is a nonspecific symptom seen in patients with chronic systolic heart failure (HEART FAILURE) or several forms of CARDIOMYOPATHIES. | 0 | 2 | 1 | 0 |
22q11.2 Deletion Syndrome [description not available] | 0 | 2 | 1 | 0 |
DiGeorge Syndrome Congenital syndrome characterized by a wide spectrum of characteristics including the absence of the THYMUS and PARATHYROID GLANDS resulting in T-cell immunodeficiency, HYPOCALCEMIA, defects in the outflow tract of the heart, and craniofacial anomalies. | 0 | 2 | 1 | 0 |
Autoimmune Thrombocytopenia [description not available] | 0 | 2 | 1 | 0 |
Purpura, Thrombocytopenic, Idiopathic Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets. It is mediated by immune mechanisms, in most cases IMMUNOGLOBULIN G autoantibodies which attach to platelets and subsequently undergo destruction by macrophages. The disease is seen in acute (affecting children) and chronic (adult) forms. | 0 | 2 | 1 | 0 |
Extramembranous Glomerulopathy [description not available] | 0 | 2 | 1 | 0 |
Glomerulonephritis, Membranous A type of glomerulonephritis that is characterized by the accumulation of immune deposits (COMPLEMENT MEMBRANE ATTACK COMPLEX) on the outer aspect of the GLOMERULAR BASEMENT MEMBRANE. It progresses from subepithelial dense deposits, to basement membrane reaction and eventual thickening of the basement membrane. | 0 | 2 | 1 | 0 |
Mushroom Poisoning Poisoning from ingestion of mushrooms, primarily from, but not restricted to, toxic varieties. | 0 | 2 | 1 | 0 |
Jet Lag [description not available] | 0 | 2 | 1 | 0 |
Peritoneal Carcinomatosis [description not available] | 0 | 2 | 1 | 0 |
Peritoneal Neoplasms Tumors or cancer of the PERITONEUM. | 0 | 2 | 1 | 0 |
Acathisia, Drug-Induced [description not available] | 0 | 2.39 | 2 | 0 |
Adrenal Cancer [description not available] | 0 | 3.6 | 3 | 0 |
ACY2 Deficiency [description not available] | 0 | 2 | 1 | 0 |
Canavan Disease A rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demeylination that gives rise to a spongy appearance. Aspartoacylase deficiency leads to an accumulation of N-acetylaspartate in astrocytes. Inheritance may be autosomal recessive or the illness may occur sporadically. This illness occurs more frequently in individuals of Ashkenazic Jewish descent. The neonatal form features the onset of hypotonia and lethargy at birth, rapidly progressing to coma and death. The infantile form features developmental delay, DYSKINESIAS, hypotonia, spasticity, blindness, and megalencephaly. The juvenile form is characterized by ATAXIA; OPTIC ATROPHY; and DEMENTIA. (From Adams et al., Principles of Neurology, 6th ed, p944; Am J Med Genet 1988 Feb;29(2):463-71) | 0 | 2 | 1 | 0 |
Basilar Steal Syndrome [description not available] | 0 | 2.38 | 2 | 0 |
Fibrosarcoma A sarcoma derived from deep fibrous tissue, characterized by bundles of immature proliferating fibroblasts with variable collagen formation, which tends to invade locally and metastasize by the bloodstream. (Stedman, 25th ed) | 0 | 2.01 | 1 | 0 |
Pain, Intractable Persistent pain that is refractory to some or all forms of treatment. | 0 | 2.01 | 1 | 0 |
EBS-DM [description not available] | 0 | 2.01 | 1 | 0 |
Epidermolysis Bullosa Simplex A form of epidermolysis bullosa characterized by serous bullae that heal without scarring. Mutations in the genes that encode KERATIN-5 and KERATIN-14 have been associated with several subtypes of epidermolysis bullosa simplex. | 0 | 2.01 | 1 | 0 |
Adenomatosis, Familial Endocrine [description not available] | 0 | 2.36 | 2 | 0 |
Hypersensitivity, Type III [description not available] | 0 | 2.36 | 2 | 0 |
Vesicoureteral Reflux [description not available] | 0 | 2.86 | 1 | 0 |
Anal Atresia [description not available] | 0 | 3.56 | 3 | 0 |
Vesico-Ureteral Reflux Retrograde flow of urine from the URINARY BLADDER into the URETER. This is often due to incompetence of the vesicoureteral valve leading to ascending bacterial infection into the KIDNEY. | 0 | 2.86 | 1 | 0 |
Benign Infantile Myoclonic Epilepsy [description not available] | 0 | 1.95 | 1 | 0 |
Epilepsies, Myoclonic A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic. | 0 | 1.95 | 1 | 0 |
Infections, Paramyxoviridae [description not available] | 0 | 1.95 | 1 | 0 |
Leukocytopenia [description not available] | 0 | 1.95 | 1 | 0 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 1.95 | 1 | 0 |
Paramyxoviridae Infections Infections with viruses of the family PARAMYXOVIRIDAE. This includes MORBILLIVIRUS INFECTIONS; RESPIROVIRUS INFECTIONS; PNEUMOVIRUS INFECTIONS; HENIPAVIRUS INFECTIONS; AVULAVIRUS INFECTIONS; and RUBULAVIRUS INFECTIONS. | 0 | 1.95 | 1 | 0 |
Tracheitis INFLAMMATION of the TRACHEA that is usually associated with RESPIRATORY TRACT INFECTIONS. | 0 | 3.27 | 2 | 0 |
Bird Pox [description not available] | 0 | 2.35 | 2 | 0 |
Infections, Reoviridae [description not available] | 0 | 2.35 | 2 | 0 |
Enlarged Liver [description not available] | 0 | 2.35 | 2 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 2.35 | 2 | 0 |
Angioma, Sclerosing [description not available] | 0 | 1.95 | 1 | 0 |
Papilloma A circumscribed benign epithelial tumor projecting from the surrounding surface; more precisely, a benign epithelial neoplasm consisting of villous or arborescent outgrowths of fibrovascular stroma covered by neoplastic cells. (Stedman, 25th ed) | 0 | 2.35 | 2 | 0 |
Histiocytoma, Benign Fibrous A benign tumor composed, wholly or in part, of cells with the morphologic characteristics of HISTIOCYTES and with various fibroblastic components. Fibrous histiocytomas can occur anywhere in the body. When they occur in the skin, they are called dermatofibromas or sclerosing hemangiomas. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 5th ed, p1747) | 0 | 1.95 | 1 | 0 |
Congenital Foot Deformities [description not available] | 0 | 1.95 | 1 | 0 |
Congenital Hand Deformities [description not available] | 0 | 2.65 | 3 | 0 |
Chemodectoma [description not available] | 0 | 1.95 | 1 | 0 |
Coronaviridae Infections Virus diseases caused by CORONAVIRIDAE. | 0 | 1.95 | 1 | 0 |
Stye [description not available] | 0 | 3.45 | 8 | 0 |
Hordeolum Purulent infection of one of the sebaceous glands of Zeis along the eyelid margin (external) or of the meibomian gland on the conjunctival side of the eyelid (internal). | 0 | 3.45 | 8 | 0 |
Bronchial Pneumonia [description not available] | 0 | 2.36 | 2 | 0 |
Tuberculosis, Bovine An infection of cattle caused by MYCOBACTERIUM BOVIS. It is transmissible to man and other animals. | 0 | 2.35 | 2 | 0 |
Thyroiditis Inflammatory diseases of the THYROID GLAND. Thyroiditis can be classified into acute (THYROIDITIS, SUPPURATIVE), subacute (granulomatous and lymphocytic), chronic fibrous (Riedel's), chronic lymphocytic (HASHIMOTO DISEASE), transient (POSTPARTUM THYROIDITIS), and other AUTOIMMUNE THYROIDITIS subtypes. | 0 | 2.36 | 2 | 0 |
Babesia Infection [description not available] | 0 | 2.87 | 1 | 0 |
Lock Jaw [description not available] | 0 | 1.95 | 1 | 0 |
Bunostomiasis [description not available] | 0 | 1.95 | 1 | 0 |
Hookworm Infections Infection of humans or animals with hookworms other than those caused by the genus Ancylostoma or Necator, for which the specific terms ANCYLOSTOMIASIS and NECATORIASIS are available. | 0 | 1.95 | 1 | 0 |
Palatal Neoplasms Tumors or cancer of the PALATE, including those of the hard palate, soft palate and UVULA. | 0 | 1.95 | 1 | 0 |
Morphine Abuse [description not available] | 0 | 1.95 | 1 | 0 |
Morphine Dependence Strong dependence, both physiological and emotional, upon morphine. | 0 | 1.95 | 1 | 0 |
Infections, Nematomorpha [description not available] | 0 | 1.95 | 1 | 0 |
Helminthiasis Infestation with parasitic worms of the helminth class. | 0 | 1.95 | 1 | 0 |
Brain Damage, Chronic A condition characterized by long-standing brain dysfunction or damage, usually of three months duration or longer. Potential etiologies include BRAIN INFARCTION; certain NEURODEGENERATIVE DISORDERS; CRANIOCEREBRAL TRAUMA; ANOXIA, BRAIN; ENCEPHALITIS; certain NEUROTOXICITY SYNDROMES; metabolic disorders (see BRAIN DISEASES, METABOLIC); and other conditions. | 0 | 2.87 | 4 | 0 |
Childhood Schizophrenia [description not available] | 0 | 1.95 | 1 | 0 |
Entamoeba histolytica Infection [description not available] | 0 | 1.95 | 1 | 0 |
Fracture, Pathologic [description not available] | 0 | 1.95 | 1 | 0 |
Adult Fanconi Syndrome [description not available] | 0 | 2.87 | 1 | 0 |
Fetal Resorption The disintegration and assimilation of the dead FETUS in the UTERUS at any stage after the completion of organogenesis which, in humans, is after the 9th week of GESTATION. It does not include embryo resorption (see EMBRYO LOSS). | 0 | 2.36 | 2 | 0 |
Abnormalities, Mouth [description not available] | 0 | 1.95 | 1 | 0 |
Water-Electrolyte Imbalance Disturbances in the body's WATER-ELECTROLYTE BALANCE. | 0 | 1.95 | 1 | 0 |
Bone Diseases, Developmental Diseases resulting in abnormal GROWTH or abnormal MORPHOGENESIS of BONES. | 0 | 2.35 | 2 | 0 |
Infections, Yersinia [description not available] | 0 | 1.95 | 1 | 0 |
Francois Dyscephalic Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Cardiovascular Pregnancy Complications [description not available] | 0 | 2.35 | 2 | 0 |
48,XXYY Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Klinefelter Syndrome A form of male HYPOGONADISM, characterized by the presence of an extra X CHROMOSOME, small TESTES, seminiferous tubule dysgenesis, elevated levels of GONADOTROPINS, low serum TESTOSTERONE, underdeveloped secondary sex characteristics, and male infertility (INFERTILITY, MALE). Patients tend to have long legs and a slim, tall stature. GYNECOMASTIA is present in many of the patients. The classic form has the karyotype 47,XXY. Several karyotype variants include 48,XXYY; 48,XXXY; 49,XXXXY, and mosaic patterns ( 46,XY/47,XXY; 47,XXY/48,XXXY, etc.). | 0 | 1.95 | 1 | 0 |
Lymphocytosis Excess of normal lymphocytes in the blood or in any effusion. | 0 | 1.95 | 1 | 0 |
Polyradiculitis [description not available] | 0 | 2.35 | 2 | 0 |
Hyponatremia Deficiency of sodium in the blood; salt depletion. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Polyradiculopathy Disease or injury involving multiple SPINAL NERVE ROOTS. Polyradiculitis refers to inflammation of multiple spinal nerve roots. | 0 | 2.35 | 2 | 0 |
Diseases of Pharynx [description not available] | 0 | 1.95 | 1 | 0 |
Arthritis, Degenerative [description not available] | 0 | 2.64 | 3 | 0 |
Osteoarthritis A progressive, degenerative joint disease, the most common form of arthritis, especially in older persons. The disease is thought to result not from the aging process but from biochemical changes and biomechanical stresses affecting articular cartilage. In the foreign literature it is often called osteoarthrosis deformans. | 0 | 2.64 | 3 | 0 |
Hyperparathyroidism A condition of abnormally elevated output of PARATHYROID HORMONE (or PTH) triggering responses that increase blood CALCIUM. It is characterized by HYPERCALCEMIA and BONE RESORPTION, eventually leading to bone diseases. PRIMARY HYPERPARATHYROIDISM is caused by parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. SECONDARY HYPERPARATHYROIDISM is increased PTH secretion in response to HYPOCALCEMIA, usually caused by chronic KIDNEY DISEASES. | 0 | 1.95 | 1 | 0 |
Meniscitis [description not available] | 0 | 2.36 | 2 | 0 |
Amyotrophic Neuralgia [description not available] | 0 | 1.95 | 1 | 0 |
Brachial Plexus Neuritis A syndrome associated with inflammation of the BRACHIAL PLEXUS. Clinical features include severe pain in the shoulder region which may be accompanied by MUSCLE WEAKNESS and loss of sensation in the upper extremity. This condition may be associated with VIRUS DISEASES; IMMUNIZATION; SURGERY; heroin use (see HEROIN DEPENDENCE); and other conditions. The term brachial neuralgia generally refers to pain associated with brachial plexus injury. (From Adams et al., Principles of Neurology, 6th ed, pp1355-6) | 0 | 1.95 | 1 | 0 |
Akinetic Autism [description not available] | 0 | 1.95 | 1 | 0 |
Infarct of the Spleen [description not available] | 0 | 1.95 | 1 | 0 |
Kidney, Polycystic [description not available] | 0 | 1.95 | 1 | 0 |
Polycystic Kidney Diseases Hereditary diseases that are characterized by the progressive expansion of a large number of tightly packed CYSTS within the KIDNEYS. They include diseases with autosomal dominant and autosomal recessive inheritance. | 0 | 1.95 | 1 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 2.36 | 2 | 0 |
Carcinoma, Hepatocellular A primary malignant neoplasm of epithelial liver cells. It ranges from a well-differentiated tumor with EPITHELIAL CELLS indistinguishable from normal HEPATOCYTES to a poorly differentiated neoplasm. The cells may be uniform or markedly pleomorphic, or form GIANT CELLS. Several classification schemes have been suggested. | 0 | 2.36 | 2 | 0 |
AIDS, Feline [description not available] | 0 | 1.98 | 1 | 0 |
Amniotic Band Syndrome A disorder present in the newborn infant in which constriction rings or bands, causing soft tissue depressions, encircle digits, extremities, or limbs and sometimes the neck, thorax, or abdomen. They may be associated with intrauterine amputations. | 0 | 2.66 | 3 | 0 |
alpha Mannosidase B Deficiency [description not available] | 0 | 3.07 | 5 | 0 |
alpha-Mannosidosis An inborn error of metabolism marked by a defect in the lysosomal isoform of ALPHA-MANNOSIDASE activity that results in lysosomal accumulation of mannose-rich intermediate metabolites. Virtually all patients have psychomotor retardation, facial coarsening, and some degree of dysostosis multiplex. It is thought to be an autosomal recessive disorder. | 0 | 3.07 | 5 | 0 |
Jaw, Edentulous, Partially Absence of teeth from a portion of the mandible and/or maxilla. | 0 | 1.98 | 1 | 0 |
Glomerulonephritis, Lupus [description not available] | 0 | 1.98 | 1 | 0 |
Lupus Nephritis Glomerulonephritis associated with autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Lupus nephritis is histologically classified into 6 classes: class I - normal glomeruli, class II - pure mesangial alterations, class III - focal segmental glomerulonephritis, class IV - diffuse glomerulonephritis, class V - diffuse membranous glomerulonephritis, and class VI - advanced sclerosing glomerulonephritis (The World Health Organization classification 1982). | 0 | 1.98 | 1 | 0 |
Infection, Wound [description not available] | 0 | 2.65 | 3 | 0 |
Coronary Artery Vasospasm [description not available] | 0 | 2.89 | 1 | 0 |
Coronary Vasospasm Spasm of the large- or medium-sized coronary arteries. | 0 | 2.89 | 1 | 0 |
Oxaluria, Primary [description not available] | 0 | 1.97 | 1 | 0 |
Urinary Calculi Low-density crystals or stones in any part of the URINARY TRACT. Their chemical compositions often include CALCIUM OXALATE, magnesium ammonium phosphate (struvite), CYSTINE, or URIC ACID. | 0 | 1.97 | 1 | 0 |
Hyperoxaluria, Primary A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism. | 0 | 1.97 | 1 | 0 |
Pulmonary Stenoses [description not available] | 0 | 1.97 | 1 | 0 |
Drug Abuse, Intravenous [description not available] | 0 | 2.89 | 1 | 0 |
Actinomycetales Infections Infections with bacteria of the order ACTINOMYCETALES. | 0 | 1.97 | 1 | 0 |
Eccentro-Osteochondrodysplasia [description not available] | 0 | 1.97 | 1 | 0 |
Mucopolysaccharidosis IV Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme. | 0 | 1.97 | 1 | 0 |
Adenomatous Polyposis Coli, Familial [description not available] | 0 | 1.97 | 1 | 0 |
Adenomatous Polyposis Coli A polyposis syndrome due to an autosomal dominant mutation of the APC genes (GENES, APC) on CHROMOSOME 5. The syndrome is characterized by the development of hundreds of ADENOMATOUS POLYPS in the COLON and RECTUM of affected individuals by early adulthood. | 0 | 1.97 | 1 | 0 |
Infections, Mycoplasmatales [description not available] | 0 | 2.89 | 4 | 0 |
Amnionitis [description not available] | 0 | 1.97 | 1 | 0 |
Chorioamnionitis INFLAMMATION of the placental membranes (CHORION; AMNION) and connected tissues such as fetal BLOOD VESSELS and UMBILICAL CORD. It is often associated with intrauterine ascending infections during PREGNANCY. | 0 | 1.97 | 1 | 0 |
Albers-Schoenberg Disease [description not available] | 0 | 1.97 | 1 | 0 |
Osteopetrosis Excessive formation of dense trabecular bone leading to pathological fractures; OSTEITIS; SPLENOMEGALY with infarct; ANEMIA; and extramedullary hemopoiesis (HEMATOPOIESIS, EXTRAMEDULLARY). | 0 | 1.97 | 1 | 0 |
Blast Phase [description not available] | 0 | 1.97 | 1 | 0 |
Blast Crisis An advanced phase of chronic myelogenous leukemia, characterized by a rapid increase in the proportion of immature white blood cells (blasts) in the blood and bone marrow to greater than 30%. | 0 | 1.97 | 1 | 0 |
Adenoma, Pleomorphic A benign, slow-growing tumor, most commonly of the salivary gland, occurring as a small, painless, firm nodule, usually of the parotid gland, but also found in any major or accessory salivary gland anywhere in the oral cavity. It is most often seen in women in the fifth decade. Histologically, the tumor presents a variety of cells: cuboidal, columnar, and squamous cells, showing all forms of epithelial growth. (Dorland, 27th ed) | 0 | 1.96 | 1 | 0 |
Extravasation of Contrast Media [description not available] | 0 | 1.97 | 1 | 0 |
Dissociative Identity Disorder A dissociative disorder in which the individual adopts two or more distinct personalities. Each personality is a fully integrated and complex unit with memories, behavior patterns and social friendships. Transition from one personality to another is sudden. | 0 | 1.97 | 1 | 0 |
P carinii Pneumonia [description not available] | 0 | 2.87 | 4 | 0 |
Pneumonia, Pneumocystis A pulmonary disease in humans occurring in immunodeficient or malnourished patients or infants, characterized by DYSPNEA, tachypnea, and HYPOXEMIA. Pneumocystis pneumonia is a frequently seen opportunistic infection in AIDS. It is caused by the fungus PNEUMOCYSTIS JIROVECII. The disease is also found in other MAMMALS where it is caused by related species of Pneumocystis. | 0 | 2.87 | 4 | 0 |
Carcinoma, Ehrlich Tumor A transplantable, poorly differentiated malignant tumor which appeared originally as a spontaneous breast carcinoma in a mouse. It grows in both solid and ascitic forms. | 0 | 2.36 | 2 | 0 |
Complex IV Deficiency [description not available] | 0 | 1.97 | 1 | 0 |
Adenoma, alpha-Cell [description not available] | 0 | 1.97 | 1 | 0 |
Island Cell Tumor [description not available] | 0 | 1.97 | 1 | 0 |
Adenoma, Islet Cell A benign tumor of the pancreatic ISLET CELLS. Usually it involves the INSULIN-producing PANCREATIC BETA CELLS, as in INSULINOMA, resulting in HYPERINSULINISM. | 0 | 1.97 | 1 | 0 |
Cystitis Inflammation of the URINARY BLADDER, either from bacterial or non-bacterial causes. Cystitis is usually associated with painful urination (dysuria), increased frequency, urgency, and suprapubic pain. | 0 | 3.28 | 2 | 0 |
Heroin Abuse [description not available] | 0 | 2.36 | 2 | 0 |
Heroin Dependence Strong dependence or addiction, both physiological and emotional, upon HEROIN. | 0 | 2.36 | 2 | 0 |
Sphingolipid Storage Diseases [description not available] | 0 | 1.96 | 1 | 0 |
Neoplasms, Nerve Tissue Neoplasms composed of nerve tissue. This concept does not refer to neoplasms located in the nervous system or its component nerves. | 0 | 2.36 | 2 | 0 |
Moniliasis, Oral [description not available] | 0 | 1.96 | 1 | 0 |
Candidiasis, Oral Infection of the mucous membranes of the mouth by a fungus of the genus CANDIDA. (Dorland, 27th ed) | 0 | 1.96 | 1 | 0 |
Convalescence The period of recovery following an illness. | 0 | 2.36 | 2 | 0 |
Cronobacter Infections [description not available] | 0 | 1.97 | 1 | 0 |
Enterobacteriaceae Infections Infections with bacteria of the family ENTEROBACTERIACEAE. | 0 | 1.97 | 1 | 0 |
Wounds, Stab Penetrating wounds caused by a pointed object. | 0 | 1.97 | 1 | 0 |
Chromosomes, Ring [description not available] | 0 | 1.96 | 1 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 2.36 | 2 | 0 |
Mitral Incompetence [description not available] | 0 | 1.96 | 1 | 0 |
Mitral Valve Insufficiency Backflow of blood from the LEFT VENTRICLE into the LEFT ATRIUM due to imperfect closure of the MITRAL VALVE. This can lead to mitral valve regurgitation. | 0 | 1.96 | 1 | 0 |
African Sleeping Sickness [description not available] | 0 | 1.97 | 1 | 0 |
Trypanosomiasis, African A disease endemic among people and animals in Central Africa. It is caused by various species of trypanosomes, particularly T. gambiense and T. rhodesiense. Its second host is the TSETSE FLY. Involvement of the central nervous system produces African sleeping sickness. Nagana is a rapidly fatal trypanosomiasis of horses and other animals. | 0 | 1.97 | 1 | 0 |
Meningitis, Meningococcal, Serogroup A [description not available] | 0 | 1.97 | 1 | 0 |
Meningitis, Meningococcal A fulminant infection of the meninges and subarachnoid fluid by the bacterium NEISSERIA MENINGITIDIS, producing diffuse inflammation and peri-meningeal venous thromboses. Clinical manifestations include FEVER, nuchal rigidity, SEIZURES, severe HEADACHE, petechial rash, stupor, focal neurologic deficits, HYDROCEPHALUS, and COMA. The organism is usually transmitted via nasopharyngeal secretions and is a leading cause of meningitis in children and young adults. Organisms from Neisseria meningitidis serogroups A, B, C, Y, and W-135 have been reported to cause meningitis. (From Adams et al., Principles of Neurology, 6th ed, pp689-701; Curr Opin Pediatr 1998 Feb;10(1):13-8) | 0 | 1.97 | 1 | 0 |
Anemia, Hemolytic, Acquired [description not available] | 0 | 2.36 | 2 | 0 |
Anemia, Hemolytic A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES). | 0 | 2.36 | 2 | 0 |
Lymphocytopenia [description not available] | 0 | 1.97 | 1 | 0 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 1.97 | 1 | 0 |
Paraneoplastic Syndromes In patients with neoplastic diseases a wide variety of clinical pictures which are indirect and usually remote effects produced by tumor cell metabolites or other products. | 0 | 2.88 | 1 | 0 |
Lentiginosis, Perioral [description not available] | 0 | 1.96 | 1 | 0 |
Peutz-Jeghers Syndrome A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits. | 0 | 1.96 | 1 | 0 |
Bile Duct Obstruction, Intrahepatic [description not available] | 0 | 1.96 | 1 | 0 |
Cholestasis, Intrahepatic Impairment of bile flow due to injury to the HEPATOCYTES; BILE CANALICULI; or the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). | 0 | 1.96 | 1 | 0 |
Hand Injuries General or unspecified injuries to the hand. | 0 | 1.96 | 1 | 0 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 1.96 | 1 | 0 |
Ciguatera [description not available] | 0 | 1.96 | 1 | 0 |
Urination Disorders Abnormalities in the process of URINE voiding, including bladder control, frequency of URINATION, as well as the volume and composition of URINE. | 0 | 1.96 | 1 | 0 |
Ciguatera Poisoning Poisoning caused by ingestion of SEAFOOD containing microgram levels of CIGUATOXINS. The poisoning is characterized by gastrointestinal, neurological and cardiovascular disturbances. | 0 | 1.96 | 1 | 0 |
Endothelioma, Vascular [description not available] | 0 | 1.96 | 1 | 0 |
Hemangioendothelioma A neoplasm derived from blood vessels, characterized by numerous prominent endothelial cells that occur singly, in aggregates, and as the lining of congeries of vascular tubes or channels. Hemangioendotheliomas are relatively rare and are of intermediate malignancy (between benign hemangiomas and conventional angiosarcomas). They affect men and women about equally and rarely develop in childhood. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1866) | 0 | 1.96 | 1 | 0 |
Lentigines [description not available] | 0 | 2.36 | 2 | 0 |
Lentigo Small circumscribed melanoses resembling, but differing histologically from, freckles. The concept includes senile lentigo ('liver spots') and nevoid lentigo (nevus spilus, lentigo simplex) and may also occur in association with multiple congenital defects or congenital syndromes (e.g., Peutz-Jeghers syndrome). | 0 | 2.36 | 2 | 0 |
Cancer of Spleen [description not available] | 0 | 1.96 | 1 | 0 |
Conductive Hearing Loss [description not available] | 0 | 1.96 | 1 | 0 |
Deficiency, IgA [description not available] | 0 | 1.96 | 1 | 0 |
Presbycusis Gradual bilateral hearing loss associated with aging that is due to progressive degeneration of cochlear structures and central auditory pathways. Hearing loss usually begins with the high frequencies then progresses to sounds of middle and low frequencies. | 0 | 1.96 | 1 | 0 |
Tricuspid Incompetence [description not available] | 0 | 1.96 | 1 | 0 |
Prediabetes [description not available] | 0 | 1.96 | 1 | 0 |
Prediabetic State The time period before the development of symptomatic diabetes. For example, certain risk factors can be observed in subjects who subsequently develop INSULIN RESISTANCE as in type 2 diabetes (DIABETES MELLITUS, TYPE 2). | 0 | 1.96 | 1 | 0 |
Blepharospasm-Oromandibular Dyskinesia [description not available] | 0 | 1.96 | 1 | 0 |
Echo Virus Infections [description not available] | 0 | 1.96 | 1 | 0 |
Intertrochanteric Fractures [description not available] | 0 | 1.96 | 1 | 0 |
Hip Fractures Fractures of the FEMUR HEAD; the FEMUR NECK; (FEMORAL NECK FRACTURES); the trochanters; or the inter- or subtrochanteric region. Excludes fractures of the acetabulum and fractures of the femoral shaft below the subtrochanteric region (FEMORAL FRACTURES). | 0 | 1.96 | 1 | 0 |
Adult Refsum Disease [description not available] | 0 | 2.35 | 2 | 0 |
Celiac Sprue [description not available] | 0 | 1.94 | 1 | 0 |
Celiac Disease A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION. | 0 | 1.94 | 1 | 0 |
Esophageal Reflux [description not available] | 0 | 2.86 | 1 | 0 |
Gastroesophageal Reflux Retrograde flow of gastric juice (GASTRIC ACID) and/or duodenal contents (BILE ACIDS; PANCREATIC JUICE) into the distal ESOPHAGUS, commonly due to incompetence of the LOWER ESOPHAGEAL SPHINCTER. | 0 | 2.86 | 1 | 0 |
Restless Leg Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Restless Legs Syndrome A disorder characterized by aching or burning sensations in the lower and rarely the upper extremities that occur prior to sleep or may awaken the patient from sleep. | 0 | 1.95 | 1 | 0 |
Hepatitis, Animal INFLAMMATION of the LIVER in non-human animals. | 0 | 2.35 | 2 | 0 |
Deficiency of Glucose-6-Phosphate Dehydrogenase [description not available] | 0 | 1.94 | 1 | 0 |
Glucosephosphate Dehydrogenase Deficiency A disease-producing enzyme deficiency subject to many variants, some of which cause a deficiency of GLUCOSE-6-PHOSPHATE DEHYDROGENASE activity in erythrocytes, leading to hemolytic anemia. | 0 | 1.94 | 1 | 0 |
Cancer of Salivary Gland [description not available] | 0 | 2.35 | 2 | 0 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 2.35 | 2 | 0 |
Mucositis, Oral [description not available] | 0 | 2.35 | 2 | 0 |
Skin Manifestations Dermatologic disorders attendant upon non-dermatologic disease or injury. | 0 | 2.35 | 2 | 0 |
Stomatitis INFLAMMATION of the soft tissues of the MOUTH, such as MUCOSA; PALATE; GINGIVA; and LIP. | 0 | 2.35 | 2 | 0 |
Vaginal Diseases Pathological processes of the VAGINA. | 0 | 1.94 | 1 | 0 |
Carbohydrate Metabolism, Inborn Error [description not available] | 0 | 2.64 | 3 | 0 |
Lipid Metabolism, Inborn Error [description not available] | 0 | 3.04 | 5 | 0 |
EHS Tumor [description not available] | 0 | 2.85 | 1 | 0 |
Cranial Nerve Injuries Dysfunction of one or more cranial nerves causally related to a traumatic injury. Penetrating and nonpenetrating CRANIOCEREBRAL TRAUMA; NECK INJURIES; and trauma to the facial region are conditions associated with cranial nerve injuries. | 0 | 1.94 | 1 | 0 |
Lipodystrophy A collection of heterogenous conditions resulting from defective LIPID METABOLISM and characterized by ADIPOSE TISSUE atrophy. Often there is redistribution of body fat resulting in peripheral fat wasting and central adiposity. They include generalized, localized, congenital, and acquired lipodystrophy. | 0 | 1.94 | 1 | 0 |
Gingivitis Inflammation of gum tissue (GINGIVA) without loss of connective tissue. | 0 | 2.35 | 2 | 0 |
Muscle Tissue Neoplasms [description not available] | 0 | 1.94 | 1 | 0 |
Middle Ear Inflammation [description not available] | 0 | 2.35 | 2 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 2.35 | 2 | 0 |
Glycosuria The appearance of an abnormally large amount of GLUCOSE in the urine, such as more than 500 mg/day in adults. It can be due to HYPERGLYCEMIA or genetic defects in renal reabsorption (RENAL GLYCOSURIA). | 0 | 1.94 | 1 | 0 |
Diabetes, Phosphate [description not available] | 0 | 1.95 | 1 | 0 |
Hypophosphatemia, Familial An inherited condition of abnormally low serum levels of PHOSPHATES (below 1 mg/liter) which can occur in a number of genetic diseases with defective reabsorption of inorganic phosphorus by the PROXIMAL RENAL TUBULES. This leads to phosphaturia, HYPOPHOSPHATEMIA, and disturbances of cellular and organ functions such as those in X-LINKED HYPOPHOSPHATEMIC RICKETS; OSTEOMALACIA; and FANCONI SYNDROME. | 0 | 1.95 | 1 | 0 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 1.95 | 1 | 0 |
Gall Bladder Diseases [description not available] | 0 | 1.95 | 1 | 0 |
Penile Diseases Pathological processes involving the PENIS or its component tissues. | 0 | 1.95 | 1 | 0 |
Nodular Goiter [description not available] | 0 | 1.95 | 1 | 0 |
Goiter, Nodular An enlarged THYROID GLAND containing multiple nodules (THYROID NODULE), usually resulting from recurrent thyroid HYPERPLASIA and involution over many years to produce the irregular enlargement. Multinodular goiters may be nontoxic or may induce THYROTOXICOSIS. | 0 | 1.95 | 1 | 0 |
Alkalosis A pathological condition that removes acid or adds base to the body fluids. | 0 | 1.95 | 1 | 0 |
Scleroma, Nasal [description not available] | 0 | 1.95 | 1 | 0 |
Rhinoscleroma A granulomatous disease caused by KLEBSIELLA RHINOSCLEROMATIS infection. Despite its name, this disease is not limited to the nose and NASOPHARYNX but may affect any part of the RESPIRATORY TRACT, sometimes with extension to the lip and the skin. | 0 | 1.95 | 1 | 0 |
Myeloproliferative Disorders Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE. | 0 | 1.95 | 1 | 0 |
Auriculotemporal Nerve Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Costen's Syndrome [description not available] | 0 | 2.35 | 2 | 0 |
Gastroenteritis, Transmissible, of Swine A condition of chronic gastroenteritis in adult pigs and fatal gastroenteritis in piglets caused by a CORONAVIRUS. | 0 | 2.86 | 1 | 0 |
Leriche Syndrome A condition caused by occlusion of terminal aorta, the primary branches of the ABDOMINAL AORTA, as in aortoiliac obstruction. Leriche syndrome usually occurs in males and is characterized by IMPOTENCE, absence of a pulse in the femoral arteries, weakness and numbness in the lower back, buttocks, hips, and lower limbs. | 0 | 2.86 | 1 | 0 |
Bilirubinemia [description not available] | 0 | 2.86 | 1 | 0 |
Hyperbilirubinemia, Hereditary Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood. | 0 | 2.86 | 1 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 2.86 | 1 | 0 |
Hemoglobinopathies A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. | 0 | 3.27 | 2 | 0 |
Slow Virus Diseases Diseases of viral origin, characterized by incubation periods of months to years, insidious onset of clinical manifestations, and protracted clinical course. Though the disease process is protracted, viral multiplication may not be unusually slow. Conventional viruses produce slow virus diseases such as SUBACUTE SCLEROSING PANENCEPHALITIS, progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL), and AIDS. Diseases produced by unconventional agents were originally considered part of this group. They are now called PRION DISEASES. | 0 | 2.86 | 1 | 0 |
Congenital Micrognathia [description not available] | 0 | 1.94 | 1 | 0 |
Maxillary Diseases Diseases involving the MAXILLA. | 0 | 1.95 | 1 | 0 |
Panniculitis, Nodular Nonsuppurative A form of panniculitis characterized by recurrent episodes of fever accompanied by the eruption of single or multiple erythematous subcutaneous nodules on the lower extremities. They normally resolve, but tend to leave depressions in the skin. The condition is most often seen in women, alone or in association with other disorders. | 0 | 1.94 | 1 | 0 |
Hydatid Mole [description not available] | 0 | 1.94 | 1 | 0 |
Hydatidiform Mole Trophoblastic hyperplasia associated with normal gestation, or molar pregnancy. It is characterized by the swelling of the CHORIONIC VILLI and elevated human CHORIONIC GONADOTROPIN. Hydatidiform moles or molar pregnancy may be categorized as complete or partial based on their gross morphology, histopathology, and karyotype. | 0 | 1.94 | 1 | 0 |
Carcinoma, Brown-Pearce A transplantable EPITHELIAL CELL neoplasm of rabbits. | 0 | 2.35 | 2 | 0 |
Exostoses Benign hypertrophy that projects outward from the surface of bone, often containing a cartilaginous component. | 0 | 1.94 | 1 | 0 |
Bronchial Diseases Diseases involving the BRONCHI. | 0 | 1.95 | 1 | 0 |
Cheyne-Stokes Respiration An abnormal pattern of breathing characterized by alternating periods of apnea and deep, rapid breathing. The cycle begins with slow, shallow breaths that gradually increase in depth and rate and is then followed by a period of apnea. The period of apnea can last 5 to 30 seconds, then the cycle repeats every 45 seconds to 3 minutes. | 0 | 2.35 | 2 | 0 |
Aperture Syndrome, Thoracic Outlet [description not available] | 0 | 1.95 | 1 | 0 |
Thoracic Outlet Syndrome A neurovascular syndrome associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the superior thoracic outlet. This may result from a variety of anomalies such as a CERVICAL RIB, anomalous fascial bands, and abnormalities of the origin or insertion of the anterior or medial scalene muscles. Clinical features may include pain in the shoulder and neck region which radiates into the arm, PARESIS or PARALYSIS of brachial plexus innervated muscles, PARESTHESIA, loss of sensation, reduction of arterial pulses in the affected extremity, ISCHEMIA, and EDEMA. (Adams et al., Principles of Neurology, 6th ed, pp214-5). | 0 | 1.95 | 1 | 0 |
Peripheral Nerve Injury [description not available] | 0 | 1.95 | 1 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 1.95 | 1 | 0 |
Acquired Meningocele [description not available] | 0 | 1.95 | 1 | 0 |
Hyperplasia of Thymus Gland [description not available] | 0 | 1.95 | 1 | 0 |
Gangrene Death and putrefaction of tissue usually due to a loss of blood supply. | 0 | 6.95 | 1 | 0 |
Mesenteric Lymphadenitis INFLAMMATION of LYMPH NODES in the MESENTERY. | 0 | 1.95 | 1 | 0 |
Bouillaud Disease [description not available] | 0 | 1.95 | 1 | 0 |
Rheumatic Heart Disease Cardiac manifestation of systemic rheumatological conditions, such as RHEUMATIC FEVER. Rheumatic heart disease can involve any part the heart, most often the HEART VALVES and the ENDOCARDIUM. | 0 | 1.95 | 1 | 0 |
Autolysis The spontaneous disintegration of tissues or cells by the action of their own autogenous enzymes. | 0 | 7.35 | 2 | 0 |
Amyotonia Congenita [description not available] | 0 | 1.95 | 1 | 0 |
Neuromuscular Diseases A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA. | 0 | 1.95 | 1 | 0 |
Armstrong Syndrome [description not available] | 0 | 1.95 | 1 | 0 |
Injuries, Prenatal [description not available] | 0 | 1.95 | 1 | 0 |
Stammering [description not available] | 0 | 2.86 | 1 | 0 |
Stuttering A disturbance in the normal fluency and time patterning of speech that is inappropriate for the individual's age. This disturbance is characterized by frequent repetitions or prolongations of sounds or syllables. Various other types of speech dysfluencies may also be involved including interjections, broken words, audible or silent blocking, circumlocutions, words produced with an excess of physical tension, and monosyllabic whole word repetitions. Stuttering may occur as a developmental condition in childhood or as an acquired disorder which may be associated with BRAIN INFARCTIONS and other BRAIN DISEASES. (From DSM-IV, 1994) | 0 | 2.86 | 1 | 0 |
Leukemia, Radiation-Induced Leukemia produced by exposure to IONIZING RADIATION or NON-IONIZING RADIATION. | 0 | 2.86 | 1 | 0 |
Coagulation Disorders, Blood [description not available] | 0 | 2.86 | 1 | 0 |
Blood Coagulation Disorders Hemorrhagic and thrombotic disorders that occur as a consequence of abnormalities in blood coagulation due to a variety of factors such as COAGULATION PROTEIN DISORDERS; BLOOD PLATELET DISORDERS; BLOOD PROTEIN DISORDERS or nutritional conditions. | 0 | 2.86 | 1 | 0 |
Priapism A prolonged painful erection that may lasts hours and is not associated with sexual activity. It is seen in patients with SICKLE CELL ANEMIA, advanced malignancy, spinal trauma; and certain drug treatments. | 0 | 3.26 | 2 | 0 |
Acidosis, Respiratory Respiratory retention of carbon dioxide. It may be chronic or acute. | 0 | 2.86 | 1 | 0 |
Halitosis An offensive, foul breath odor resulting from a variety of causes such as poor oral hygiene, dental or oral infections, or the ingestion of certain foods. | 0 | 2.35 | 2 | 0 |
Laryngitis Inflammation of the LARYNGEAL MUCOSA, including the VOCAL CORDS. Laryngitis is characterized by irritation, edema, and reduced pliability of the mucosa leading to VOICE DISORDERS such as APHONIA and HOARSENESS. | 0 | 1.94 | 1 | 0 |
Nail Abnormalities [description not available] | 0 | 1.94 | 1 | 0 |
Femoral Hernia [description not available] | 0 | 2.86 | 1 | 0 |
Ventricular Fibrillation A potentially lethal cardiac arrhythmia that is characterized by uncoordinated extremely rapid firing of electrical impulses (400-600/min) in HEART VENTRICLES. Such asynchronous ventricular quivering or fibrillation prevents any effective cardiac output and results in unconsciousness (SYNCOPE). It is one of the major electrocardiographic patterns seen with CARDIAC ARREST. | 0 | 6.94 | 1 | 0 |
Lichen Simplex Chronicus [description not available] | 0 | 1.94 | 1 | 0 |
Branchial Cleft Cyst [description not available] | 0 | 1.94 | 1 | 0 |
Neurodermatitis An extremely variable eczematous skin disease that is presumed to be a response to prolonged vigorous scratching, rubbing, or pinching to relieve intense pruritus. It varies in intensity, severity, course, and morphologic expression in different individuals. Neurodermatitis is believed by some to be psychogenic. The circumscribed or localized form is often referred to as lichen simplex chronicus. | 0 | 1.94 | 1 | 0 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 1.94 | 1 | 0 |
Transfusion Reaction Complications of BLOOD TRANSFUSION. Included adverse reactions are common allergic and febrile reactions; hemolytic (delayed and acute) reactions; and other non-hemolytic adverse reactions such as infections and adverse immune reactions related to immunocompatibility. | 0 | 1.94 | 1 | 0 |
Enteritis Inflammation of any segment of the SMALL INTESTINE. | 0 | 1.94 | 1 | 0 |
Calculus, Dental [description not available] | 0 | 1.94 | 1 | 0 |
Dental Plaque A film that attaches to teeth, often causing DENTAL CARIES and GINGIVITIS. It is composed of MUCINS, secreted from salivary glands, and microorganisms. | 0 | 1.94 | 1 | 0 |
Dental Deposit [description not available] | 0 | 1.94 | 1 | 0 |
Central European Encephalitis [description not available] | 0 | 1.94 | 1 | 0 |
Diaper Rashes [description not available] | 0 | 1.94 | 1 | 0 |
Diaper Rash A type of irritant dermatitis localized to the area in contact with a diaper and occurring most often as a reaction to prolonged contact with urine, feces, or retained soap or detergent. | 0 | 1.94 | 1 | 0 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 1.94 | 1 | 0 |
Cancer of the Uterus [description not available] | 0 | 1.94 | 1 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 1.94 | 1 | 0 |
Bezoars Concretions of swallowed hair, fruit or vegetable fibers, or similar substances found in the alimentary canal. | 0 | 1.94 | 1 | 0 |
Liver Steatosis [description not available] | 0 | 1.94 | 1 | 0 |
Fatty Liver Lipid infiltration of the hepatic parenchymal cells resulting in a yellow-colored liver. The abnormal lipid accumulation is usually in the form of TRIGLYCERIDES, either as a single large droplet or multiple small droplets. Fatty liver is caused by an imbalance in the metabolism of FATTY ACIDS. | 0 | 1.94 | 1 | 0 |
Anterior Fascicular Block [description not available] | 0 | 1.94 | 1 | 0 |
Cerebromalacia [description not available] | 0 | 1.94 | 1 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 1.94 | 1 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 1.94 | 1 | 0 |
Hypogalactia A condition of less than normal MILK secretion. | 0 | 1.94 | 1 | 0 |
Tick Toxicoses Toxicoses caused by toxic substances secreted by the salivary glands of ticks; include tick paralysis (neurotropic toxin), sweating sickness (dermotropic toxin), and Rhipicephalus appendiculatus toxicosis (leukotropic toxin). | 0 | 1.94 | 1 | 0 |
Kerion Celsi An inflammatory manifestation of tinea capitis with a pronounced swelling that develops into suppurative central and indurated peripheral area called kerion. | 0 | 1.94 | 1 | 0 |
Tinea Capitis Ringworm of the scalp and associated hair mainly caused by species of MICROSPORUM; TRICHOPHYTON; and EPIDERMOPHYTON, which may occasionally involve the eyebrows and eyelashes. | 0 | 1.94 | 1 | 0 |
Colorado Tick Fever A febrile illness characterized by chills, aches, vomiting, leukopenia, and sometimes encephalitis. It is caused by the COLORADO TICK FEVER VIRUS, a reovirus transmitted by the tick Dermacentor andersoni. | 0 | 1.94 | 1 | 0 |
Candidiasis, Genital [description not available] | 0 | 1.94 | 1 | 0 |
Trichomoniasis, Human [description not available] | 0 | 1.94 | 1 | 0 |
Candidiasis, Vulvovaginal Infection of the VULVA and VAGINA with a fungus of the genus CANDIDA. | 0 | 1.94 | 1 | 0 |
Trichomonas Vaginitis Inflammation of the vagina, marked by a purulent discharge. This disease is caused by the protozoan TRICHOMONAS VAGINALIS. | 0 | 1.94 | 1 | 0 |
Hemorrhage, Uterine [description not available] | 0 | 1.94 | 1 | 0 |
Uterine Hemorrhage Bleeding from blood vessels in the UTERUS, sometimes manifested as vaginal bleeding. | 0 | 1.94 | 1 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 1.94 | 1 | 0 |
Abdominal Pregnancy [description not available] | 0 | 1.94 | 1 | 0 |
Pregnancy, Tubal The most common ( | 0 | 1.94 | 1 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 1.94 | 1 | 0 |
Disgerminoma [description not available] | 0 | 1.94 | 1 | 0 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 1.94 | 1 | 0 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 1.94 | 1 | 0 |
Dysgerminoma A malignant ovarian neoplasm, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. It is the counterpart of the classical seminoma of the testis, to which it is both grossly and histologically identical. Dysgerminomas comprise 16% of all germ cell tumors but are rare before the age of 10, although nearly 50% occur before the age of 20. They are generally considered of low-grade malignancy but may spread if the tumor extends through its capsule and involves lymph nodes or blood vessels. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1646) | 0 | 1.94 | 1 | 0 |
Heavy Menstrual Bleeding [description not available] | 0 | 1.94 | 1 | 0 |
Menorrhagia Excessive uterine bleeding during MENSTRUATION. | 0 | 1.94 | 1 | 0 |
Bertielliasis [description not available] | 0 | 1.94 | 1 | 0 |