Benign Neoplasms [description not available] | 0 | 8.11 | 240 | 0 |
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 | 8.11 | 240 | 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 | 16.06 | 280 | 14 |
Innate Inflammatory Response [description not available] | 0 | 19.01 | 168 | 52 |
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 | 19.01 | 168 | 52 |
Encephalitis, Polio [description not available] | 0 | 3.64 | 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 | 3.64 | 10 | 0 |
Plasmodium falciparum Malaria [description not available] | 0 | 2.48 | 2 | 0 |
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 | 2.48 | 2 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 13.29 | 62 | 8 |
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 | 13.29 | 62 | 8 |
Congenital Zika Syndrome [description not available] | 0 | 2.59 | 2 | 0 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 10.43 | 153 | 0 |
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 | 2.59 | 2 | 0 |
Basilar Impression [description not available] | 0 | 4.08 | 5 | 0 |
Fibroid [description not available] | 0 | 3.11 | 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 | 3.11 | 5 | 0 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 14.59 | 344 | 4 |
Cancer of Lip [description not available] | 0 | 6.14 | 31 | 0 |
Cancer of Skin [description not available] | 0 | 16.63 | 456 | 7 |
Cancer of Nose [description not available] | 0 | 16.68 | 987 | 6 |
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 | 14.59 | 344 | 4 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 16.63 | 456 | 7 |
Ciliary Dyskinesia [description not available] | 0 | 7.93 | 25 | 0 |
Ciliary Dyskinesia, Primary, 1 [description not available] | 0 | 9.16 | 19 | 2 |
Ciliary Motility Disorders Conditions caused by abnormal CILIA movement in the body, usually causing KARTAGENER SYNDROME, chronic respiratory disorders, chronic SINUSITIS, and chronic OTITIS. Abnormal ciliary beating is likely due to defects in any of the 200 plus ciliary proteins, such as missing motor enzyme DYNEIN arms. | 0 | 7.93 | 25 | 0 |
Breathlessness [description not available] | 0 | 9.81 | 27 | 3 |
Dyspnea Difficult or labored breathing. | 0 | 9.81 | 27 | 3 |
2019 Novel Coronavirus Disease [description not available] | 0 | 18.89 | 352 | 4 |
Cadaver A dead body, usually a human body. | 0 | 12.7 | 244 | 3 |
Facial Asymmetry Congenital or acquired asymmetry of the face. | 0 | 11.26 | 140 | 2 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 9.62 | 54 | 1 |
Nasal Bleeding [description not available] | 0 | 18.56 | 362 | 27 |
Epistaxis Bleeding from the nose. | 0 | 18.56 | 362 | 27 |
Recrudescence [description not available] | 0 | 15.53 | 177 | 7 |
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 | 9 | 63 | 1 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 4.92 | 12 | 0 |
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 | 4.92 | 12 | 0 |
Local Neoplasm Recurrence [description not available] | 0 | 10.35 | 151 | 0 |
Harelip [description not available] | 0 | 22.3 | 1,454 | 36 |
Cleft Palate, Isolated [description not available] | 0 | 20.81 | 974 | 27 |
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 | 22.3 | 1,454 | 36 |
Cleft Palate Congenital fissure of the soft and/or hard palate, due to faulty fusion. | 0 | 20.81 | 974 | 27 |
B Virus Infection [description not available] | 0 | 8.84 | 48 | 2 |
Equine Diseases [description not available] | 0 | 9.85 | 72 | 3 |
Alobar Holoprosencephaly [description not available] | 0 | 7.06 | 36 | 0 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 14.94 | 316 | 6 |
Adrenocorticotropic Hormone, Inappropriate Secretion [description not available] | 0 | 4.67 | 9 | 0 |
Adenoma, Basal Cell [description not available] | 0 | 13.96 | 128 | 3 |
Cancer of Pituitary [description not available] | 0 | 16.11 | 242 | 7 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 13.96 | 128 | 3 |
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 | 16.11 | 242 | 7 |
Pituitary ACTH Hypersecretion A disease of the PITUITARY GLAND characterized by the excess amount of ADRENOCORTICOTROPIC HORMONE secreted. This leads to hypersecretion of cortisol (HYDROCORTISONE) by the ADRENAL GLANDS resulting in CUSHING SYNDROME. | 0 | 4.67 | 9 | 0 |
Nasal Diseases [description not available] | 0 | 18.95 | 893 | 7 |
Infections, Pneumococcal [description not available] | 0 | 10.53 | 54 | 4 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 10.53 | 54 | 4 |
Bilateral Nasal Obstruction [description not available] | 0 | 20.47 | 592 | 21 |
Molar, Fourth [description not available] | 0 | 7.18 | 30 | 0 |
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. | 1 | 22.47 | 592 | 21 |
Bites, Human Bites inflicted by humans. | 0 | 5.21 | 19 | 0 |
Acquired Nasal Deformities [description not available] | 0 | 17.33 | 857 | 5 |
Complication, Postoperative [description not available] | 0 | 21.31 | 722 | 49 |
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 | 21.31 | 722 | 49 |
Apnea, Obstructive Sleep [description not available] | 0 | 19.59 | 228 | 43 |
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 | 19.59 | 228 | 43 |
Dermatoses [description not available] | 0 | 7.83 | 99 | 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 | 13.06 | 58 | 7 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 7.83 | 99 | 0 |
Airway Obstruction Any hindrance to the passage of air into and out of the lungs. | 0 | 17.59 | 295 | 11 |
Glossoptosis, Micrognathia, and Cleft Palate [description not available] | 0 | 4.92 | 14 | 0 |
Abdominal Migraine [description not available] | 0 | 7 | 18 | 1 |
Day Blindness [description not available] | 0 | 7.22 | 34 | 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 | 7 | 18 | 1 |
Viral Diseases [description not available] | 0 | 11.45 | 65 | 3 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 11.45 | 65 | 3 |
Extranodal NK-T-Cell Lymphoma [description not available] | 0 | 5.47 | 12 | 0 |
Viremia The presence of viruses in the blood. | 0 | 5.58 | 16 | 1 |
Respiratory Tract Diseases Diseases involving the RESPIRATORY SYSTEM. | 0 | 13.94 | 129 | 1 |
Atypical Lipoma [description not available] | 0 | 5.91 | 17 | 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 | 5.91 | 17 | 0 |
Allergic Rhinitis [description not available] | 0 | 14.34 | 88 | 5 |
Asthma, Bronchial [description not available] | 0 | 17.37 | 203 | 16 |
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 | 17.37 | 203 | 16 |
Rhinitis, Allergic An inflammation of the NASAL MUCOSA triggered by ALLERGENS. | 0 | 14.34 | 88 | 5 |
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 | 5.7 | 7 | 1 |
Bovine Diseases [description not available] | 0 | 9.82 | 98 | 4 |
Infections, Pasteurella [description not available] | 0 | 6.5 | 26 | 2 |
Infections, Pasteurellaceae [description not available] | 0 | 2.79 | 3 | 0 |
Infantile Respiratory Distress Syndrome [description not available] | 0 | 14.83 | 65 | 20 |
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 | 14.83 | 65 | 20 |
Fungal Diseases [description not available] | 0 | 7.42 | 63 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 7.42 | 63 | 0 |
Diathesis [description not available] | 0 | 6.83 | 24 | 0 |
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 | 7.5 | 48 | 0 |
Hereditary Hemorrhagic Telangiectasia [description not available] | 0 | 6.93 | 27 | 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 | 6.93 | 27 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 17.7 | 153 | 28 |
Chronic Illness [description not available] | 0 | 17.65 | 251 | 15 |
Sinus Infections [description not available] | 0 | 19.25 | 426 | 14 |
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 | 17.65 | 251 | 15 |
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 | 13.88 | 203 | 7 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 1 | 21.25 | 426 | 14 |
Infections, Orthomyxoviridae [description not available] | 0 | 7.07 | 79 | 1 |
Orthomyxoviridae Infections Virus diseases caused by the ORTHOMYXOVIRIDAE. | 0 | 7.07 | 79 | 1 |
Symptom Cluster [description not available] | 0 | 13.67 | 422 | 0 |
Syndrome A characteristic symptom complex. | 0 | 13.67 | 422 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 9.24 | 84 | 1 |
Angiofibroma A benign neoplasm of fibrous tissue in which there are numerous small and large, frequently dilated, vascular channels. (Stedman, 25th ed) | 0 | 6.68 | 28 | 0 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 9.24 | 84 | 1 |
Acute Confusional Senile Dementia [description not available] | 0 | 5.85 | 9 | 0 |
Nasal Catarrh [description not available] | 0 | 19.94 | 440 | 26 |
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 | 5.85 | 9 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 1 | 21.94 | 440 | 26 |
Bed Sores [description not available] | 0 | 9.01 | 19 | 6 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 21.03 | 268 | 21 |
Pressure Ulcer An ulceration caused by prolonged pressure on the SKIN and TISSUES when one stays in one position for a long period of time, such as lying in bed. The bony areas of the body are the most frequently affected sites which become ischemic (ISCHEMIA) under sustained and constant pressure. | 0 | 9.01 | 19 | 6 |
Respiratory Insufficiency Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) | 0 | 21.03 | 268 | 21 |
Mouth Breathing Abnormal breathing through the mouth, usually associated with obstructive disorders of the nasal passages. | 0 | 13.09 | 175 | 6 |
Dermoid [description not available] | 0 | 7.94 | 78 | 0 |
Infections, Staphylococcal [description not available] | 0 | 22.46 | 1,012 | 67 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 22.46 | 1,012 | 67 |
Cerebrospinal Fluid Drainage [description not available] | 0 | 8.19 | 51 | 0 |
Neoplasms, Skull Base [description not available] | 0 | 9.85 | 140 | 0 |
Ache [description not available] | 0 | 12.5 | 64 | 23 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 12.5 | 64 | 23 |
Atresia, Choanal [description not available] | 0 | 10.17 | 103 | 1 |
Angioma, Cavernous A tumor-like mass with large vascular space that is filled with blood or lymph. | 0 | 5.86 | 22 | 0 |
Orbital Neoplasms Neoplasms of the bony orbit and contents except the eyeball. | 0 | 7.08 | 36 | 0 |
Apnea, Sleep [description not available] | 0 | 15.59 | 161 | 15 |
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 | 15.59 | 161 | 15 |
Snoring Rough, noisy breathing during sleep, due to vibration of the uvula and soft palate. | 0 | 12.78 | 84 | 9 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 13.63 | 468 | 1 |
Eye Foreign Bodies Inanimate objects that become enclosed in the eye. | 0 | 5.08 | 10 | 0 |
Teeth, Impacted [description not available] | 0 | 5.99 | 14 | 0 |
Infections, Respiratory [description not available] | 0 | 15.54 | 262 | 11 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 1 | 17.54 | 262 | 11 |
Cacosmia [description not available] | 0 | 14.76 | 98 | 6 |
Granulomatosis, Wegener's [description not available] | 0 | 9.14 | 63 | 1 |
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 | 9.14 | 63 | 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 | 6.17 | 17 | 0 |
Diseases, Occupational [description not available] | 0 | 10.17 | 49 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 7.69 | 41 | 0 |
Stunted Growth [description not available] | 0 | 9.77 | 60 | 1 |
Cochlear Hearing Loss [description not available] | 0 | 7.56 | 36 | 0 |
Central Hypothyroidism [description not available] | 0 | 7.55 | 37 | 0 |
Deficiency, Mental [description not available] | 0 | 11.55 | 137 | 2 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 7.53 | 35 | 0 |
Anal Atresia [description not available] | 0 | 7.4 | 35 | 0 |
Anhidrotic Ectodermal Dysplasia [description not available] | 0 | 7.94 | 50 | 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 | 9.77 | 60 | 1 |
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 | 7.56 | 36 | 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 | 7.55 | 37 | 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 | 11.55 | 137 | 2 |
Neurilemoma [description not available] | 0 | 7.14 | 47 | 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 | 7.14 | 47 | 0 |
Keratoderma Blennorrhagicum [description not available] | 0 | 5.58 | 17 | 1 |
Abnormalities, Skin [description not available] | 0 | 5.98 | 26 | 0 |
Verruca [description not available] | 0 | 2.49 | 2 | 0 |
Keratosis Any horny growth such as a wart or callus. | 0 | 5.58 | 17 | 1 |
Skin Abnormalities Congenital structural abnormalities of the skin. | 0 | 5.98 | 26 | 0 |
Warts Benign epidermal proliferations or tumors; some are viral in origin. | 0 | 2.49 | 2 | 0 |
Craniofacial Abnormalities Congenital structural deformities, malformations, or other abnormalities of the cranium and facial bones. | 0 | 10.6 | 122 | 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 | 4.82 | 12 | 0 |
Bacterial Disease [description not available] | 0 | 11.88 | 68 | 5 |
Corynebacterium Infections Infections with bacteria of the genus CORYNEBACTERIUM. | 0 | 3.39 | 7 | 0 |
Moraxella Infections [description not available] | 0 | 3.03 | 4 | 0 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 11.88 | 68 | 5 |
Acrocephaly Premature closing of the lambdoid and coronal sutures. | 0 | 9.76 | 52 | 1 |
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 | 9.76 | 52 | 1 |
Mucorales Infection [description not available] | 0 | 6.64 | 35 | 0 |
Orbital Diseases Diseases of the bony orbit and contents except the eyeball. | 0 | 6.96 | 32 | 0 |
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 | 6.64 | 35 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 3.27 | 6 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 8.3 | 50 | 1 |
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 | 8.3 | 50 | 1 |
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 | 10.89 | 101 | 1 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 3.93 | 12 | 0 |
Rhinorrhea Excess nasal drainage. | 0 | 6.55 | 4 | 1 |
Anoxemia [description not available] | 0 | 14.68 | 66 | 15 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 14.68 | 66 | 15 |
Acute Idiopathic Facial Neuropathy [description not available] | 0 | 2.9 | 2 | 0 |
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 | 2.9 | 2 | 0 |
Brachydactylia [description not available] | 0 | 3.4 | 6 | 0 |
Hair Diseases Diseases affecting the orderly growth and persistence of hair. | 0 | 9.01 | 61 | 1 |
Albright Hereditary Osteodystrophy [description not available] | 0 | 2.41 | 1 | 0 |
Acrodysplasia V [description not available] | 0 | 7.22 | 46 | 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 | 2.41 | 1 | 0 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 4.15 | 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 | 4.03 | 5 | 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 | 4.15 | 6 | 0 |
Infections, Respiratory Syncytial Virus [description not available] | 0 | 9.46 | 51 | 3 |
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 | 9.46 | 51 | 3 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 10.36 | 29 | 5 |
Abnormalities, Respiratory System [description not available] | 0 | 8.15 | 38 | 0 |
Infections, Coronavirus [description not available] | 0 | 15.22 | 250 | 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 | 15.22 | 250 | 0 |
Acquired Encephalocele [description not available] | 0 | 9.67 | 93 | 1 |
Germinoblastoma [description not available] | 0 | 3.83 | 12 | 0 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 3.83 | 12 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 7.9 | 52 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 10.81 | 37 | 4 |
Allergic Reaction [description not available] | 0 | 13.3 | 167 | 9 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 1 | 15.3 | 167 | 9 |
Cranial Airocele [description not available] | 0 | 6.04 | 20 | 0 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 8.35 | 56 | 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 | 6.49 | 31 | 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 | 8.35 | 56 | 0 |
Bone Cancer [description not available] | 0 | 5.2 | 19 | 0 |
Breast Cancer [description not available] | 0 | 3.07 | 5 | 0 |
Sarcoma, Epithelioid [description not available] | 0 | 5.46 | 16 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 4.15 | 6 | 0 |
Cystosarcoma Phyllodes [description not available] | 0 | 2.41 | 1 | 0 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 5.2 | 19 | 0 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 3.07 | 5 | 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 | 5.67 | 18 | 0 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 5.46 | 16 | 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 | 4.15 | 6 | 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 | 4.45 | 8 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 16.55 | 475 | 2 |
Adverse Drug Event [description not available] | 0 | 6.8 | 5 | 1 |
Bronchiolitis Inflammation of the BRONCHIOLES. | 0 | 10.39 | 22 | 1 |
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 | 6.8 | 5 | 1 |
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 | 5.76 | 15 | 0 |
Dysphagia [description not available] | 0 | 8.59 | 32 | 2 |
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 | 8.59 | 32 | 2 |
Inadequate Velopharyngeal Closure [description not available] | 0 | 10.28 | 97 | 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 | 10.61 | 68 | 5 |
Infections, Pseudomonas [description not available] | 0 | 6.68 | 21 | 1 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 6.68 | 21 | 1 |
Disease Exacerbation [description not available] | 0 | 10.92 | 40 | 5 |
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 | 4.36 | 21 | 0 |
Epidermal Cyst Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules. | 0 | 5.42 | 14 | 0 |
Asymptomatic Conditions [description not available] | 0 | 3.43 | 6 | 0 |
Cellulitis, Orbital [description not available] | 0 | 2.37 | 2 | 0 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 9.11 | 64 | 0 |
Scleroma, Nasal [description not available] | 0 | 6.76 | 38 | 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 | 6.76 | 38 | 0 |
Viral Zoonoses Viral infections that may be transmitted between non-human animals and HUMANS. | 0 | 2.41 | 1 | 0 |
Infection Reactivation [description not available] | 0 | 3.07 | 3 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 5.41 | 24 | 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 | 2.41 | 1 | 0 |
Brain Disorders [description not available] | 0 | 6.89 | 31 | 0 |
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 | 6.89 | 31 | 0 |
Maggot Infestations [description not available] | 0 | 8.54 | 50 | 1 |
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 | 4.99 | 15 | 0 |
Pink Eye [description not available] | 0 | 7.08 | 20 | 1 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 7.08 | 20 | 1 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 9.28 | 139 | 1 |
Oral Fistula An abnormal passage within the mouth communicating between two or more anatomical structures. | 0 | 4.87 | 33 | 0 |
Adenoma, Prolactin-Secreting, Pituitary [description not available] | 0 | 6.21 | 7 | 1 |
Hyperdactyly [description not available] | 0 | 5.22 | 8 | 0 |
Amelia [description not available] | 0 | 5.55 | 10 | 0 |
Congenital Foot Deformities [description not available] | 0 | 7.28 | 33 | 0 |
Congenital Hand Deformities [description not available] | 0 | 7.72 | 46 | 0 |
Earache Pain in the ear. | 0 | 2.52 | 2 | 0 |
Itching [description not available] | 0 | 8.68 | 18 | 4 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 1 | 10.68 | 18 | 4 |
Disseminated Fungal Infection [description not available] | 0 | 3.32 | 5 | 0 |
Eyelid Diseases Diseases involving the EYELIDS. | 0 | 8.53 | 18 | 0 |
Eyelid Neoplasms Tumors of cancer of the EYELIDS. | 0 | 6.12 | 30 | 0 |
6th Nerve Palsy [description not available] | 0 | 2.57 | 2 | 0 |
Endothelioma, Vascular [description not available] | 0 | 2.25 | 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 | 2.25 | 1 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 13.27 | 223 | 3 |
Canine Diseases [description not available] | 0 | 9.75 | 119 | 2 |
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 | 13.27 | 223 | 3 |
Dysembryoma [description not available] | 0 | 4.19 | 18 | 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 | 4.19 | 18 | 0 |
Hypopharyngeal Cancer [description not available] | 0 | 4.2 | 3 | 1 |
Hypopharyngeal Neoplasms Tumors or cancer of the HYPOPHARYNX. | 0 | 4.2 | 3 | 1 |
Osteoradionecrosis Necrosis of bone following radiation injury. | 0 | 2.9 | 4 | 0 |
Aneurysmal Bone Cysts [description not available] | 0 | 3.53 | 2 | 0 |
Health Care Associated Infection [description not available] | 0 | 17.41 | 287 | 18 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 17.41 | 287 | 18 |
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 | 8.2 | 44 | 0 |
Exanthem [description not available] | 0 | 6.22 | 12 | 1 |
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 | 6.22 | 12 | 1 |
Benign Meningeal Neoplasms [description not available] | 0 | 9.56 | 59 | 1 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 9.56 | 59 | 1 |
Sleepiness Compelling urge to sleep. | 0 | 3.98 | 3 | 0 |
Hyperkinetic Dysphonia [description not available] | 0 | 3.33 | 1 | 0 |
Aprosodia [description not available] | 0 | 10.33 | 99 | 3 |
Dysphonia Difficulty and/or pain in PHONATION or speaking. | 0 | 3.33 | 1 | 0 |
Anasarca [description not available] | 0 | 12.8 | 54 | 5 |
Edema, Laryngeal [description not available] | 0 | 3.98 | 5 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 12.8 | 54 | 5 |
Laryngeal Edema Abnormal accumulation of fluid in tissues of any part of the LARYNX, commonly associated with laryngeal injuries and allergic reactions. | 0 | 3.98 | 5 | 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 | 4.93 | 37 | 0 |
Degloving Injuries Avulsions of the superficial tissues of SKIN and SUBCUTANEOUS TISSUE from the underlying FASCIA. | 0 | 3.51 | 2 | 0 |
Erysipeloid An infection caused by Erysipelothrix rhusiopathiae that is almost wholly restricted to persons who in their occupation handle infected fish, shellfish, poultry, or meat. Three forms of this condition exist: a mild localized form manifested by local swelling and redness of the skin; a diffuse form that might present with fever; and a rare systemic form associated with endocarditis. | 0 | 2.54 | 2 | 0 |
Leishmaniasis, American [description not available] | 0 | 4.1 | 15 | 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 | 4.1 | 15 | 0 |
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 | 13.6 | 49 | 6 |
Middle Ear Inflammation [description not available] | 0 | 10.66 | 66 | 4 |
Koch's Disease [description not available] | 0 | 6.61 | 52 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 10.66 | 66 | 4 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 6.61 | 52 | 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 | 14.1 | 181 | 5 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 14.1 | 181 | 5 |
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 | 11.49 | 90 | 2 |
Branch Vein Occlusion [description not available] | 0 | 3.22 | 3 | 0 |
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 | 3.22 | 3 | 0 |
Angioneurotic Edema [description not available] | 0 | 3.39 | 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 | 3.39 | 7 | 0 |
Nasal Septal Perforation An opening or hole in the NASAL SEPTUM that is caused by TRAUMA, injury, drug use, or pathological process. | 0 | 5.33 | 12 | 0 |
Bilateral Headache [description not available] | 0 | 11.53 | 70 | 5 |
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 | 11.53 | 70 | 5 |
Hamartoma A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area. | 0 | 4.96 | 14 | 0 |
Atrial Septal Defect [description not available] | 0 | 3.11 | 5 | 0 |
Esophagotracheal Fistula [description not available] | 0 | 3.36 | 7 | 0 |
Behavior Disorders [description not available] | 0 | 5.7 | 20 | 0 |
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 | 5.7 | 20 | 0 |
Apnea A transient absence of spontaneous respiration. | 0 | 10.46 | 33 | 4 |
Prolapse The protrusion of an organ or part of an organ into a natural or artificial orifice. | 0 | 2.67 | 3 | 0 |
Angioblastic Meningioma [description not available] | 0 | 9.86 | 69 | 1 |
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 | 9.86 | 69 | 1 |
Chronic Lung Injury [description not available] | 0 | 5 | 3 | 1 |
Acute Respiratory Distress Syndrome [description not available] | 0 | 11.15 | 26 | 1 |
Respiratory Distress Syndrome A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA. | 0 | 11.15 | 26 | 1 |
Deficiency Syndrome, Leukocyte-Adhesion [description not available] | 0 | 2.41 | 1 | 0 |
Leukocyte-Adhesion Deficiency Syndrome Rare, autosomal recessive disorder caused by deficiency of the beta 2 integrin receptors (RECEPTORS, LEUKOCYTE-ADHESION) comprising the CD11/CD18 family of glycoproteins. The syndrome is characterized by abnormal adhesion-dependent functions, especially defective tissue emigration of neutrophils, leading to recurrent infection. | 0 | 2.41 | 1 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 6.41 | 30 | 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 | 6.41 | 30 | 0 |
Bleb [description not available] | 0 | 4.16 | 6 | 0 |
Hand Foot and Mouth Disease [description not available] | 0 | 2.41 | 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 | 2.41 | 1 | 0 |
Anophthalmia [description not available] | 0 | 6.69 | 25 | 0 |
Benign Cranial Nerve Neoplasms [description not available] | 0 | 6.04 | 17 | 0 |
Aneurysm, False Not an aneurysm but a well-defined collection of blood and CONNECTIVE TISSUE outside the wall of a blood vessel or the heart. It is the containment of a ruptured blood vessel or heart, such as sealing a rupture of the left ventricle. False aneurysm is formed by organized THROMBUS and HEMATOMA in surrounding tissue. | 0 | 4.71 | 6 | 0 |
Carotid Arteriopathies, Traumatic [description not available] | 0 | 5.47 | 14 | 0 |
Cocaine Abuse [description not available] | 0 | 5.51 | 15 | 0 |
Cocaine-Related Disorders Disorders related or resulting from use of cocaine. | 0 | 5.51 | 15 | 0 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 11.53 | 145 | 1 |
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 | 2.41 | 1 | 0 |
Angle's Classification [description not available] | 0 | 13.04 | 211 | 4 |
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 | 13.04 | 211 | 4 |
Papilloma, Inverted A mucosal tumor of the urinary bladder or nasal cavity in which proliferating epithelium is invaginated beneath the surface and is more smoothly rounded than in other papillomas. (Stedman, 25th ed) | 0 | 7.27 | 26 | 0 |
Myelopathy [description not available] | 0 | 3.33 | 1 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 5.44 | 5 | 1 |
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 | 3.33 | 1 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 6.71 | 7 | 1 |
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 | 6.71 | 7 | 1 |
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 | 4.34 | 4 | 0 |
Grippe [description not available] | 0 | 13.52 | 148 | 19 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 8.97 | 135 | 1 |
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 | 13.52 | 148 | 19 |
Abnormalities, Maxillofacial [description not available] | 0 | 7.76 | 51 | 0 |
Conjugate Nystagmus [description not available] | 0 | 4.15 | 6 | 0 |
Concomitant Strabismus [description not available] | 0 | 6.03 | 20 | 0 |
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 | 6.03 | 20 | 0 |
Margins of Excision The edges of tissue removed in a surgery for assessment of the effectiveness of a surgical procedure in achieving the local control of a neoplasm and the adequacy of tumor removal. When the margin is negative or not involved by tumor (e.g., CANCER) it suggests all of the tumor has been removed by the surgery. | 0 | 3.32 | 5 | 0 |
Blow Out Fracture [description not available] | 0 | 9.23 | 67 | 1 |
Enophthalmos Recession of the eyeball into the orbit. | 0 | 3.58 | 8 | 0 |
Cancer of Paranasal Sinus [description not available] | 0 | 11.64 | 182 | 1 |
Paranasal Sinus Neoplasms Tumors or cancer of the PARANASAL SINUSES. | 0 | 11.64 | 182 | 1 |
Deafness, Transitory [description not available] | 0 | 5.32 | 22 | 0 |
Granulomas [description not available] | 0 | 7.28 | 74 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 7.28 | 74 | 0 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 5.32 | 22 | 0 |
Endotoxin Shock [description not available] | 0 | 6.46 | 24 | 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. | 1 | 8.46 | 24 | 0 |
Weight Reduction [description not available] | 0 | 6.35 | 7 | 2 |
Weight Loss Decrease in existing BODY WEIGHT. | 0 | 6.35 | 7 | 2 |
Daytime Sleepiness [description not available] | 0 | 5.02 | 3 | 1 |
Disorders of Excessive Somnolence Disorders characterized by hypersomnolence during normal waking hours that may impair cognitive functioning. Subtypes include primary hypersomnia disorders (e.g., IDIOPATHIC HYPERSOMNOLENCE; NARCOLEPSY; and KLEINE-LEVIN SYNDROME) and secondary hypersomnia disorders where excessive somnolence can be attributed to a known cause (e.g., drug affect, MENTAL DISORDERS, and SLEEP APNEA SYNDROME). (From J Neurol Sci 1998 Jan 8;153(2):192-202; Thorpy, Principles and Practice of Sleep Medicine, 2nd ed, p320) | 0 | 5.02 | 3 | 1 |
Calcification, Pathologic [description not available] | 0 | 6.28 | 16 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 6.28 | 16 | 0 |
Inferior Dislocation [description not available] | 0 | 7.44 | 29 | 1 |
Cranial Nerve III Diseases [description not available] | 0 | 3.25 | 5 | 0 |
Angiosarcoma [description not available] | 0 | 5.78 | 20 | 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 | 5.78 | 20 | 0 |
Dysgeusia A condition characterized by alterations of the sense of taste which may range from mild to severe, including gross distortions of taste quality. | 0 | 4.02 | 9 | 0 |
Cancer, Embryonal [description not available] | 0 | 4.92 | 12 | 0 |
Neoplasms, Germ Cell and Embryonal Neoplasms composed of primordial GERM CELLS of embryonic GONADS or of elements of the germ layers of the EMBRYO, MAMMALIAN. The concept does not refer to neoplasms located in the gonads or present in an embryo or FETUS. | 0 | 4.92 | 12 | 0 |
Linear Skull Fracture [description not available] | 0 | 12.36 | 232 | 3 |
Acne [description not available] | 0 | 14.37 | 88 | 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 | 14.37 | 88 | 3 |
Abnormalities, Musculoskeletal [description not available] | 0 | 3.55 | 8 | 0 |
Cancer of Lung [description not available] | 0 | 5.49 | 25 | 0 |
Ovine Diseases [description not available] | 0 | 8.61 | 53 | 2 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 5.49 | 25 | 0 |
Hypermelanosis [description not available] | 0 | 4.73 | 9 | 0 |
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 | 4.73 | 9 | 0 |
Allotriophagy An unusual desire or craving for abnormal foods. | 0 | 3.24 | 5 | 0 |
Bone Fractures [description not available] | 0 | 12.35 | 262 | 1 |
Fractures, Bone Breaks in bones. | 0 | 12.35 | 262 | 1 |
Rhinitis, Allergic, Nonseasonal [description not available] | 0 | 17.02 | 129 | 18 |
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 | 17.02 | 129 | 18 |
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 | 5.01 | 9 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 6.94 | 32 | 0 |
Cataract, Membranous [description not available] | 0 | 3.68 | 10 | 0 |
Eye Disorders [description not available] | 0 | 9.99 | 60 | 0 |
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) | 1 | 5.68 | 10 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 9.99 | 60 | 0 |
Paranasal Sinus Diseases Diseases affecting or involving the PARANASAL SINUSES and generally manifesting as inflammation, abscesses, cysts, or tumors. | 0 | 11.84 | 140 | 1 |
Secondary Hyperparathyroidism [description not available] | 0 | 2.6 | 1 | 0 |
Hyperparathyroidism, Secondary Abnormally elevated PARATHYROID HORMONE secretion as a response to HYPOCALCEMIA. It is caused by chronic KIDNEY FAILURE or other abnormalities in the controls of bone and mineral metabolism, leading to various BONE DISEASES, such as RENAL OSTEODYSTROPHY. | 0 | 2.6 | 1 | 0 |
Hay Fever [description not available] | 0 | 20.8 | 296 | 84 |
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. | 1 | 22.8 | 296 | 84 |
Glioma, Subependymal Rare, slow-growing, benign intraventricular tumors, often asymptomatic and discovered incidentally. The tumors are classified histologically as ependymomas and demonstrate a proliferation of subependymal fibrillary astrocytes among the ependymal tumor cells. (From Clin Neurol Neurosurg 1997 Feb;99(1):17-22) | 0 | 2.6 | 1 | 0 |
Dentofacial Abnormalities [description not available] | 0 | 3.25 | 5 | 0 |
Cancer of Head [description not available] | 0 | 8.07 | 74 | 0 |
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 | 8.07 | 74 | 0 |
Facial Palsy [description not available] | 0 | 7.1 | 32 | 0 |
Cancer of Ovary [description not available] | 0 | 2.41 | 1 | 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 | 2.41 | 1 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 2.92 | 4 | 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 | 2.92 | 4 | 0 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 10.96 | 112 | 1 |
Pachymeningitis [description not available] | 0 | 6.47 | 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 | 6.47 | 32 | 0 |
ENT Diseases [description not available] | 0 | 11.91 | 108 | 2 |
Anastomotic Leak Breakdown of the connection and subsequent leakage of effluent (fluids, secretions, air) from a SURGICAL ANASTOMOSIS of the digestive, respiratory, genitourinary, and cardiovascular systems. Most common leakages are from the breakdown of suture lines in gastrointestinal or bowel anastomosis. | 0 | 2.93 | 3 | 0 |
Disbacteriosis [description not available] | 0 | 5.27 | 9 | 0 |
Breathing Sounds [description not available] | 0 | 13.86 | 286 | 0 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 13.86 | 286 | 0 |
Abnormalities, Congenital [description not available] | 0 | 9.73 | 146 | 0 |
Facio-Scapulo-Humeral Dystrophy [description not available] | 0 | 5.1 | 8 | 0 |
Muscular Dystrophy, Facioscapulohumeral An autosomal dominant degenerative muscle disease characterized by slowly progressive weakness of the muscles of the face, upper-arm, and shoulder girdle. The onset of symptoms usually occurs in the first or second decade of life. Affected individuals usually present with impairment of upper extremity elevation. This tends to be followed by facial weakness, primarily involving the orbicularis oris and orbicularis oculi muscles. (Neuromuscul Disord 1997;7(1):55-62; Adams et al., Principles of Neurology, 6th ed, p1420) | 0 | 5.1 | 8 | 0 |
Mouth, Edentulous Total lack of teeth through disease or extraction. | 0 | 6.33 | 14 | 1 |
ADPKD [description not available] | 0 | 2.6 | 1 | 0 |
Polycystic Kidney, Autosomal Dominant Kidney disorders with autosomal dominant inheritance and characterized by multiple CYSTS in both KIDNEYS with progressive deterioration of renal function. | 0 | 2.6 | 1 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 4.29 | 20 | 0 |
Choledocholithiasis Presence or formation of GALLSTONES in the COMMON BILE DUCT. | 0 | 4.44 | 4 | 1 |
Airflow Obstruction, Chronic [description not available] | 0 | 12.12 | 32 | 8 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 12.12 | 32 | 8 |
Haemophilus Infections Infections with bacteria of the genus HAEMOPHILUS. | 0 | 5.56 | 27 | 0 |
Anosmia Complete or severe loss of the subjective sense of smell. Loss of smell may be caused by many factors such as a cold, allergy, OLFACTORY NERVE DISEASES, viral RESPIRATORY TRACT INFECTIONS (e.g., COVID-19), aging and various neurological disorders (e.g., ALZHEIMER DISEASE). | 0 | 4.45 | 3 | 0 |
Dysesthesia [description not available] | 0 | 3.81 | 11 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 5.25 | 20 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 5.25 | 20 | 0 |
Adenocystic Carcinoma [description not available] | 0 | 6 | 27 | 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 | 6 | 27 | 0 |
Central Nervous System Infection [description not available] | 0 | 2.79 | 3 | 0 |
Abnormalities, Congenital, Nervous System [description not available] | 0 | 2.91 | 4 | 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 | 7.3 | 48 | 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 | 7.3 | 48 | 0 |
Constriction, Pathological [description not available] | 0 | 9.43 | 64 | 1 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 9.43 | 64 | 1 |
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 | 3.78 | 3 | 0 |
Keratitis, Ulcerative [description not available] | 0 | 2.39 | 2 | 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 | 2.39 | 2 | 0 |
Air Sickness [description not available] | 0 | 2.6 | 1 | 0 |
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 | 2.6 | 1 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 4.67 | 10 | 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 | 4.67 | 10 | 0 |
Agenesis of Hemidiaphragm [description not available] | 0 | 3.24 | 6 | 0 |
Bronchopulmonary Sequestration A developmental anomaly in which a mass of nonfunctioning lung tissue lacks normal connection with the tracheobroncheal tree and receives an anomalous blood supply originating from the descending thoracic or abdominal aorta. The mass may be extralobar, i.e., completely separated from normally connected lung, or intralobar, i.e., partly surrounded by normal lung. | 0 | 2.6 | 1 | 0 |
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 | 3.24 | 6 | 0 |
Acute Post-operative Pain [description not available] | 0 | 11.66 | 39 | 18 |
Pain, Postoperative Pain during the period after surgery. | 0 | 11.66 | 39 | 18 |
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 | 3.9 | 3 | 0 |
Acrania [description not available] | 0 | 4.15 | 6 | 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 | 4.15 | 6 | 0 |
Destombes-Rosai-Dorfman Syndrome [description not available] | 0 | 3.14 | 5 | 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 | 3.14 | 5 | 0 |
Acute Disease Disease having a short and relatively severe course. | 0 | 15.68 | 131 | 10 |
Dirofilariasis Infection with nematodes of the genus DIROFILARIA, usually in animals, especially dogs, but occasionally in man. | 0 | 2.6 | 1 | 0 |
Amputation, Traumatic Loss of a limb or other bodily appendage by accidental injury. | 0 | 6.89 | 48 | 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 | 2.6 | 1 | 0 |
Middle Ear Effusion [description not available] | 0 | 9.27 | 20 | 3 |
Otitis Media with Effusion Inflammation of the middle ear with a clear pale yellow-colored transudate. | 0 | 9.27 | 20 | 3 |
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 | 2.78 | 3 | 0 |
T-Cell Lymphoma [description not available] | 0 | 5.43 | 14 | 1 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 5.43 | 14 | 1 |
IgG4 Related Systemic Disease [description not available] | 0 | 3.92 | 3 | 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 | 3.92 | 3 | 0 |
Eosinophilic Granuloma of Soft Tissue [description not available] | 0 | 2.6 | 1 | 0 |
Cancer of the Thyroid [description not available] | 0 | 3.61 | 9 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 3.61 | 9 | 0 |
Bordetella Infections Infections with bacteria of the genus BORDETELLA. | 0 | 5.8 | 22 | 1 |
Benign Neoplasms, Brain [description not available] | 0 | 6.78 | 43 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 2.4 | 2 | 0 |
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 | 6.78 | 43 | 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 | 2.4 | 2 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 5.63 | 18 | 0 |
Sporothrix brasiliensis Infection [description not available] | 0 | 3.62 | 9 | 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 | 3.62 | 9 | 0 |
Angle Class II [description not available] | 0 | 9.86 | 106 | 6 |
Maxillary Neoplasms Cancer or tumors of the MAXILLA or upper jaw. | 0 | 4.76 | 31 | 0 |
Astrocytoma, Grade IV [description not available] | 0 | 3.31 | 2 | 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 | 3.31 | 2 | 0 |
Ptosis, Eyelid [description not available] | 0 | 5.82 | 22 | 0 |
Palsy [description not available] | 0 | 12.3 | 38 | 0 |
Blepharoptosis Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle. | 0 | 5.82 | 22 | 0 |
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 | 12.3 | 38 | 0 |
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 | 5.62 | 6 | 0 |
Fracture, Pathologic [description not available] | 0 | 4.17 | 3 | 1 |
Emphysema, Subcutaneous [description not available] | 0 | 3.97 | 13 | 0 |
Lymphoma, T Cell, Peripheral [description not available] | 0 | 2.6 | 1 | 0 |
Emphysema, Mediastinal [description not available] | 0 | 3.6 | 9 | 0 |
Lymphoma, T-Cell, Peripheral A group of malignant lymphomas thought to derive from peripheral T-lymphocytes in lymph nodes and other nonlymphoid sites. They include a broad spectrum of lymphocyte morphology, but in all instances express T-cell markers admixed with epithelioid histiocytes, plasma cells, and eosinophils. Although markedly similar to large-cell immunoblastic lymphoma (LYMPHOMA, LARGE-CELL, IMMUNOBLASTIC), this group's unique features warrant separate treatment. | 0 | 2.6 | 1 | 0 |
Patent Foramen Ovale [description not available] | 0 | 5.08 | 3 | 1 |
Branch Retinal Artery Occlusion [description not available] | 0 | 4.28 | 6 | 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 | 4.28 | 6 | 0 |
Foramen Ovale, Patent A condition in which the FORAMEN OVALE in the ATRIAL SEPTUM fails to close shortly after birth. This results in abnormal communications between the two upper chambers of the heart. An isolated patent ovale foramen without other structural heart defects is usually of no hemodynamic significance. | 0 | 5.08 | 3 | 1 |
Deaf Mutism [description not available] | 0 | 7.53 | 52 | 0 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 7.53 | 52 | 0 |
Chemical Dependence [description not available] | 0 | 5.21 | 12 | 0 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 5.21 | 12 | 0 |
Diabetic Feet [description not available] | 0 | 3.1 | 4 | 0 |
Alloxan Diabetes [description not available] | 0 | 2.6 | 1 | 0 |
Diabetic Foot Common foot problems in persons with DIABETES MELLITUS, caused by any combination of factors such as DIABETIC NEUROPATHIES; PERIPHERAL VASCULAR DISEASES; and INFECTION. With the loss of sensation and poor circulation, injuries and infections often lead to severe foot ulceration, GANGRENE and AMPUTATION. | 0 | 3.1 | 4 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 9.36 | 53 | 2 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 10.4 | 105 | 1 |
Child Mental Disorders [description not available] | 0 | 3.95 | 3 | 0 |
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 | 3.52 | 1 | 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 | 3.95 | 3 | 0 |
Angle Class III [description not available] | 0 | 11.23 | 122 | 5 |
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 | 2.72 | 3 | 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 | 12.9 | 73 | 13 |
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. | 1 | 14.9 | 73 | 13 |
Respiration Disorders Diseases of the respiratory system in general or unspecified or for a specific respiratory disease not available. | 0 | 7.05 | 31 | 0 |
Tracheal Diseases Diseases involving the TRACHEA. | 0 | 7.79 | 10 | 0 |
Dermatitis Medicamentosa [description not available] | 0 | 3.54 | 8 | 0 |
Ectoparasitic Infestations Infestations by PARASITES which live on, or burrow into, the surface of their host's EPIDERMIS. Most ectoparasites are ARTHROPODS. | 0 | 4.15 | 5 | 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 | 4.65 | 10 | 0 |
Microphthalmia [description not available] | 0 | 6.94 | 39 | 0 |
Lassitude [description not available] | 0 | 4.62 | 6 | 1 |
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 | 4.62 | 6 | 1 |
Angioma, Sclerosing [description not available] | 0 | 5.24 | 20 | 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 | 5.24 | 20 | 0 |
Dacryoadenitis [description not available] | 0 | 6.05 | 47 | 0 |
Ocular Tuberculosis [description not available] | 0 | 2.21 | 1 | 0 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 2.21 | 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 | 2.21 | 1 | 0 |
Community Acquired Infection [description not available] | 0 | 12.43 | 89 | 7 |
Phlegmon [description not available] | 0 | 6.12 | 17 | 0 |
Cronobacter Infections [description not available] | 0 | 4.71 | 11 | 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 | 6.12 | 17 | 0 |
Enterobacteriaceae Infections Infections with bacteria of the family ENTEROBACTERIACEAE. | 0 | 4.71 | 11 | 0 |
Cirrhosis [description not available] | 0 | 9.04 | 18 | 1 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 9.04 | 18 | 1 |
C gattii Infection [description not available] | 0 | 3.78 | 11 | 0 |
Cerebromeningitis [description not available] | 0 | 3.68 | 10 | 0 |
Cryptococcosis Fungal infection caused by genus CRYPTOCOCCUS. | 0 | 3.78 | 11 | 0 |
Hematologic Malignancies [description not available] | 0 | 2.8 | 3 | 0 |
Candida Infection [description not available] | 0 | 3.48 | 8 | 0 |
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 | 3.48 | 8 | 0 |
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 | 2.8 | 3 | 0 |
Athletic Injuries Injuries incurred during participation in competitive or non-competitive sports. | 0 | 7 | 29 | 0 |
Chest Injuries [description not available] | 0 | 3.3 | 2 | 0 |
Injuries, Neck [description not available] | 0 | 5.54 | 17 | 0 |
Abdominal Injuries General or unspecified injuries involving organs in the abdominal cavity. | 0 | 3.8 | 2 | 0 |
Facial Injuries General or unspecified injuries to the soft tissue or bony portions of the face. | 0 | 14.93 | 272 | 5 |
Surgical Incision [description not available] | 0 | 6.7 | 16 | 1 |
Arterial Inflammation [description not available] | 0 | 3.12 | 5 | 0 |
Bites [description not available] | 0 | 7.58 | 62 | 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 | 4.94 | 14 | 0 |
Drug Abuse, Intravenous [description not available] | 0 | 2.21 | 1 | 0 |
Adolescent Obesity [description not available] | 0 | 2.21 | 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 | 2.67 | 3 | 0 |
Angiogenesis, Pathologic [description not available] | 0 | 5.24 | 4 | 1 |
Brain Dead [description not available] | 0 | 2.94 | 4 | 0 |
Co-infection [description not available] | 0 | 5.6 | 15 | 1 |
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 | 2.69 | 3 | 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 | 3.24 | 6 | 0 |
Icterus [description not available] | 0 | 2.21 | 1 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 4.97 | 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 | 2.21 | 1 | 0 |
Bacterial Pneumonia [description not available] | 0 | 3.11 | 5 | 0 |
Infections, Klebsiella [description not available] | 0 | 3.93 | 13 | 0 |
Klebsiella Infections Infections with bacteria of the genus KLEBSIELLA. | 0 | 3.93 | 13 | 0 |
Pneumonia, Bacterial Inflammation of the lung parenchyma that is caused by bacterial infections. | 0 | 3.11 | 5 | 0 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 12.88 | 45 | 13 |
Ecchymosis Extravasation of blood into the skin, resulting in a nonelevated, rounded or irregular, blue or purplish patch, larger than a petechia. | 0 | 10.16 | 13 | 2 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 3.49 | 8 | 0 |
Enterovirus Infections Diseases caused by ENTEROVIRUS. | 0 | 3.7 | 10 | 0 |
Dermatitis, Contact, Phototoxic [description not available] | 0 | 2.49 | 2 | 0 |
Marfan Syndrome, Type I [description not available] | 0 | 2.73 | 3 | 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 | 2.73 | 3 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 5.4 | 14 | 1 |
Hyperidrosis [description not available] | 0 | 3.82 | 12 | 0 |
Papulosquamous Disorders [description not available] | 0 | 3.9 | 13 | 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 | 3.82 | 12 | 0 |
Infections, Parvoviridae [description not available] | 0 | 3.65 | 9 | 0 |
Deep Bite [description not available] | 0 | 5.3 | 12 | 1 |
Aspiration, Respiratory [description not available] | 0 | 7.31 | 8 | 1 |
MS (Multiple Sclerosis) [description not available] | 0 | 3.33 | 2 | 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 | 3.33 | 2 | 0 |
Acquired Autoimmune Hemolytic Anemia [description not available] | 0 | 3.38 | 2 | 0 |
Anemia, Hemolytic, Autoimmune Acquired hemolytic anemia due to the presence of AUTOANTIBODIES which agglutinate or lyse the patient's own RED BLOOD CELLS. | 0 | 3.38 | 2 | 0 |
Pemphigus Foliaceus [description not available] | 0 | 5.36 | 22 | 0 |
Pemphigus Group of chronic blistering diseases characterized histologically by ACANTHOLYSIS and blister formation within the EPIDERMIS. | 0 | 5.36 | 22 | 0 |
Brain Injuries, Penetrating [description not available] | 0 | 4.58 | 9 | 0 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 2.45 | 2 | 0 |
Wounds, Gunshot Disruption of structural continuity of the body as a result of the discharge of firearms. | 0 | 6.49 | 45 | 0 |
Suicidal Ideation A risk factor for suicide attempts and completions, it is the most common of all suicidal behavior, but only a minority of ideators engage in overt self-harm. | 0 | 2.25 | 1 | 0 |
Aspirin Induced Asthma [description not available] | 0 | 2.25 | 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 | 2.83 | 3 | 0 |
Dermatitis, Irritant A non-allergic contact dermatitis caused by prolonged exposure to irritants and not explained by delayed hypersensitivity mechanisms. | 0 | 2.21 | 1 | 0 |
Catastrophic Illness An acute or prolonged illness usually considered to be life-threatening or with the threat of serious residual disability. Treatment may be radical and is frequently costly. | 0 | 2.21 | 1 | 0 |
Anti-Phospholipid Antibody Syndrome [description not available] | 0 | 2.52 | 2 | 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 | 2.52 | 2 | 0 |
Bone Loss, Osteoclastic [description not available] | 0 | 3.78 | 11 | 0 |
Electron Transport Chain Deficiencies, Mitochondrial [description not available] | 0 | 3.12 | 1 | 0 |
Steatorrhea A condition that is characterized by chronic fatty DIARRHEA, a result of abnormal DIGESTION and/or INTESTINAL ABSORPTION of FATS. | 0 | 3.57 | 2 | 0 |
Chronic Pancreatitis [description not available] | 0 | 3.12 | 1 | 0 |
Lipid Metabolism, Inborn Error [description not available] | 0 | 3.12 | 1 | 0 |
Muscle Disorders [description not available] | 0 | 3.62 | 3 | 0 |
Pancreatic Insufficiency [description not available] | 0 | 6.02 | 12 | 0 |
Child Malnutrition Malnutrition occurring in children ages 2 to 12 years, which is due to insufficient intake of food, dietary nutrients, or a pathophysiologic condition which prevents the absorption and utilization of food. Growth and development are markedly affected. | 0 | 3.12 | 1 | 0 |
Congenital Lipomatosis of Pancreas [description not available] | 0 | 3.12 | 1 | 0 |
Bone Marrow Failure Syndromes, Congenital [description not available] | 0 | 3.12 | 1 | 0 |
Shwachman-Diamond Syndrome An inherited syndrome characterized by EXOCRINE PANCREATIC INSUFFICIENCY; hematologic abnormalities (e.g., bone marrow hypoplasia), and skeletal abnormalities (e.g., metaphyseal chondroplasia). GERMLINE MUTATIONS in the SBDS gene are associated with Shwachman-Diamond Syndrome. | 0 | 3.12 | 1 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 3.62 | 3 | 0 |
Exocrine Pancreatic Insufficiency A malabsorption condition resulting from greater than 10% reduction in the secretion of pancreatic digestive enzymes (LIPASE; PROTEASES; and AMYLASE) by the EXOCRINE PANCREAS into the DUODENUM. This condition is often associated with CYSTIC FIBROSIS and with chronic PANCREATITIS. | 0 | 6.02 | 12 | 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 | 3.12 | 1 | 0 |
Pancreatitis, Chronic INFLAMMATION of the PANCREAS that is characterized by recurring or persistent ABDOMINAL PAIN with or without STEATORRHEA or DIABETES MELLITUS. It is characterized by the irregular destruction of the pancreatic parenchyma which may be focal, segmental, or diffuse. | 0 | 3.12 | 1 | 0 |
Acrorenoocular Syndrome [description not available] | 0 | 2.48 | 2 | 0 |
Group A Strep Infection [description not available] | 0 | 9.59 | 65 | 3 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 9.59 | 65 | 3 |
Complications, Pregnancy [description not available] | 0 | 6.8 | 24 | 0 |
Female Genital Neoplasms [description not available] | 0 | 3.12 | 1 | 0 |
Male Genital Neoplasms [description not available] | 0 | 3.12 | 1 | 0 |
Auricular Cancer [description not available] | 0 | 5.22 | 12 | 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 | 5.22 | 12 | 0 |
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 |
Sore Throat [description not available] | 0 | 14.88 | 55 | 21 |
Pharyngitis Inflammation of the throat (PHARYNX). | 0 | 14.88 | 55 | 21 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 11.71 | 26 | 5 |
Peripheral Nerve Diseases [description not available] | 0 | 3.2 | 6 | 0 |
Epileptiform Neuralgia [description not available] | 0 | 5.18 | 19 | 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 | 3.2 | 6 | 0 |
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 | 5.18 | 19 | 0 |
Adenovirus Infections [description not available] | 0 | 6.61 | 20 | 1 |
Altered Level of Consciousness [description not available] | 0 | 3.17 | 1 | 0 |
MODS [description not available] | 0 | 4.79 | 2 | 1 |
Circulatory Collapse [description not available] | 0 | 4.08 | 3 | 0 |
Adenoviridae Infections Virus diseases caused by the ADENOVIRIDAE. | 0 | 6.61 | 20 | 1 |
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 | 4.79 | 2 | 1 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 16.62 | 235 | 1 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 4.08 | 3 | 0 |
Bronze Diabetes [description not available] | 0 | 2.52 | 2 | 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 | 2.52 | 2 | 0 |
Barrett Epithelium [description not available] | 0 | 5.52 | 8 | 2 |
Esophageal Varices [description not available] | 0 | 4.51 | 5 | 1 |
Barrett Esophagus A condition with damage to the lining of the lower ESOPHAGUS resulting from chronic acid reflux (ESOPHAGITIS, REFLUX). Through the process of metaplasia, the squamous cells are replaced by a columnar epithelium with cells resembling those of the INTESTINE or the salmon-pink mucosa of the STOMACH. Barrett's columnar epithelium is a marker for severe reflux and precursor to ADENOCARCINOMA of the esophagus. | 0 | 5.52 | 8 | 2 |
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 | 4.51 | 5 | 1 |
Brain Stem Neoplasms, Primary [description not available] | 0 | 3.02 | 4 | 0 |
Cavernous Angioma, Central Nervous System [description not available] | 0 | 2.89 | 3 | 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 | 3.02 | 4 | 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 | 2.89 | 3 | 0 |
Infant, Premature, Diseases Diseases that occur in PREMATURE INFANTS. | 0 | 12.18 | 29 | 8 |
Benign Psychomotor Epilepsy, Childhood [description not available] | 0 | 3.8 | 11 | 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 | 3.8 | 11 | 0 |
Vision, Diminished [description not available] | 0 | 2.78 | 3 | 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 | 5.31 | 11 | 1 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 12.58 | 82 | 3 |
Pneumothorax, Primary Spontaneous [description not available] | 0 | 4.75 | 7 | 1 |
Transient Tachypnea of Newborn [description not available] | 0 | 5.39 | 2 | 2 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 12.58 | 82 | 3 |
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 | 4.75 | 7 | 1 |
Amaurosis [description not available] | 0 | 6.22 | 33 | 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 | 6.22 | 33 | 0 |
Bone Cysts Benign unilocular lytic areas in the proximal end of a long bone with well defined and narrow endosteal margins. The cysts contain fluid and the cyst walls may contain some giant cells. Bone cysts usually occur in males between the ages 3-15 years. | 0 | 3.09 | 5 | 0 |
Corynebacterium diphtheriae Infection [description not available] | 0 | 5.81 | 23 | 1 |
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 | 5.81 | 23 | 1 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 6.27 | 17 | 0 |
Duncan Disease [description not available] | 0 | 2.31 | 1 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 2.31 | 1 | 0 |
Infections, Rubulavirus [description not available] | 0 | 2.5 | 2 | 0 |
Rubulavirus Infections Infections with viruses of the genus RUBULAVIRUS, family PARAMYXOVIRIDAE. | 0 | 2.5 | 2 | 0 |
Body Dysmorphic Disorders Preoccupations with appearance or self-image causing significant distress or impairment in important areas of functioning. | 0 | 3.13 | 5 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 6.26 | 13 | 1 |
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 | 6.26 | 13 | 1 |
Cyst [description not available] | 0 | 7.33 | 61 | 0 |
Aqueductal Stenosis [description not available] | 0 | 5.82 | 16 | 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 | 5.43 | 8 | 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 | 4.33 | 4 | 0 |
Altidudinal Hemianopia [description not available] | 0 | 3.25 | 6 | 0 |
Entrapment Neuropathies [description not available] | 0 | 3.84 | 4 | 0 |
Retinal Diseases Diseases involving the RETINA. | 0 | 2.92 | 4 | 0 |
Colicky Pain [description not available] | 0 | 3.17 | 1 | 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 | 3.17 | 1 | 0 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 3.17 | 1 | 0 |
Acute Edematous Pancreatitis [description not available] | 0 | 5.67 | 7 | 3 |
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 | 5.67 | 7 | 3 |
Neurologic Voice Disorder [description not available] | 0 | 5.59 | 28 | 0 |
Voice Disorders Pathological processes that affect voice production, usually involving VOCAL CORDS and the LARYNGEAL MUCOSA. Voice disorders can be caused by organic (anatomical), or functional (emotional or psychological) factors leading to DYSPHONIA; APHONIA; and defects in VOICE QUALITY, loudness, and pitch. | 0 | 5.59 | 28 | 0 |
Malignant Melanoma [description not available] | 0 | 8.75 | 62 | 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 | 8.75 | 62 | 1 |
Aspergillus Infection [description not available] | 0 | 4.39 | 21 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 4.39 | 21 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 12.85 | 92 | 6 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 5.47 | 16 | 1 |
Dermatitis Any inflammation of the skin. | 0 | 6.28 | 26 | 0 |
Apoplexy, Pituitary [description not available] | 0 | 3.13 | 4 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 11.98 | 90 | 5 |
Hypergonadotropic Hypogonadism [description not available] | 0 | 6.73 | 13 | 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 | 6.73 | 13 | 0 |
Complication, Intraoperative [description not available] | 0 | 10.27 | 38 | 2 |
Autosomal Recessive Chronic Granulomatous Disease [description not available] | 0 | 4.17 | 6 | 0 |
Granulomatous Disease, Chronic A defect of leukocyte function in which phagocytic cells ingest but fail to digest bacteria, resulting in recurring bacterial infections with granuloma formation. When chronic granulomatous disease is caused by mutations in the CYBB gene, the condition is inherited in an X-linked recessive pattern. When chronic granulomatous disease is caused by CYBA, NCF1, NCF2, or NCF4 gene mutations, the condition is inherited in an autosomal recessive pattern. | 0 | 4.17 | 6 | 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 | 6.91 | 32 | 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 | 7.79 | 37 | 2 |
Blood Loss, Postoperative [description not available] | 0 | 8.48 | 27 | 6 |
Actinic Keratosis [description not available] | 0 | 3.92 | 4 | 0 |
Keratoacanthoma A benign, non-neoplastic, usually self-limiting epithelial lesion closely resembling squamous cell carcinoma clinically and histopathologically. It occurs in solitary, multiple, and eruptive forms. The solitary and multiple forms occur on sunlight exposed areas and are identical histologically; they affect primarily white males. The eruptive form usually involves both sexes and appears as a generalized papular eruption. | 0 | 4.99 | 15 | 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 | 3.92 | 4 | 0 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 6.77 | 12 | 2 |
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 | 6.77 | 12 | 2 |
Jaw, Edentulous The total absence of teeth from either the mandible or the maxilla, but not both. Total absence of teeth from both is MOUTH, EDENTULOUS. Partial absence of teeth in either is JAW, EDENTULOUS, PARTIALLY. | 0 | 2.94 | 4 | 0 |
Laryngeal Diseases Pathological processes involving any part of the LARYNX which coordinates many functions such as voice production, breathing, swallowing, and coughing. | 0 | 9.49 | 29 | 2 |
Acrocephalosyndactylia Congenital craniostenosis with syndactyly. | 0 | 6.51 | 17 | 0 |
Idiopathic Parkinson Disease [description not available] | 0 | 5.7 | 11 | 0 |
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 | 5.7 | 11 | 0 |
Infections, Picornaviridae [description not available] | 0 | 7.24 | 19 | 2 |
Muscular Weakness [description not available] | 0 | 3.67 | 3 | 0 |
Congenital Immunodeficiency Disease [description not available] | 0 | 3.55 | 2 | 0 |
Primary Immunodeficiency Diseases Genetic immunologic deficiency diseases and syndromes due to mutations in genes involved in IMMUNITY generally characterized by an increased susceptibility to infectious diseases. They are often associated with AUTOIMMUNE DISEASE manifestations. | 0 | 3.55 | 2 | 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 | 3.67 | 3 | 0 |
Acquired Meningocele [description not available] | 0 | 5.81 | 36 | 0 |
Benign Intracranial Hypertension [description not available] | 0 | 4.51 | 5 | 0 |
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 | 4.51 | 5 | 0 |
Pneumonia, Pneumococcal A febrile disease caused by STREPTOCOCCUS PNEUMONIAE. | 0 | 4.49 | 5 | 1 |
Bone Hypertrophy [description not available] | 0 | 2.38 | 2 | 0 |
Infection [description not available] | 0 | 9.19 | 39 | 2 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 1 | 11.19 | 39 | 2 |
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 | 5.18 | 11 | 0 |
Dermatomycoses Superficial infections of the skin or its appendages by any of various fungi. | 0 | 6.18 | 23 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 14.28 | 159 | 1 |
Entomophthoramycosis [description not available] | 0 | 5.21 | 11 | 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 | 5.21 | 11 | 0 |
Acinetobacter Infections Infections with bacteria of the genus ACINETOBACTER. | 0 | 3 | 4 | 0 |
Zoonoses Diseases of non-human animals that may be transmitted to HUMANS or may be transmitted from humans to non-human animals. | 0 | 5.22 | 19 | 0 |
External Ear Inflammation [description not available] | 0 | 3.47 | 8 | 0 |
Otitis Externa Inflammation of the OUTER EAR including the external EAR CANAL, cartilages of the auricle (EAR CARTILAGE), and the TYMPANIC MEMBRANE. | 0 | 3.47 | 8 | 0 |
ACTH-Producing Pituitary Adenoma [description not available] | 0 | 3.97 | 4 | 0 |
Freckle, Melanotic [description not available] | 0 | 4.01 | 13 | 0 |
Suffocation [description not available] | 0 | 4.35 | 21 | 0 |
Asphyxia A pathological condition caused by lack of oxygen, manifested in impending or actual cessation of life. | 0 | 4.35 | 21 | 0 |
Caries, Dental [description not available] | 0 | 5.12 | 18 | 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 | 5.12 | 18 | 0 |
Carotid Artery Narrowing [description not available] | 0 | 2.25 | 1 | 0 |
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 | 2.25 | 1 | 0 |
ANCA-Associated Vasculitides [description not available] | 0 | 5.4 | 4 | 1 |
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 | 5.4 | 4 | 1 |
Capillaria hepatica Infection [description not available] | 0 | 3.96 | 4 | 0 |
Parasitic Diseases, Animal Animal diseases caused by PARASITES. | 0 | 5.29 | 4 | 1 |
Canine Distemper [description not available] | 0 | 2.76 | 3 | 0 |
Staphylococcal Pneumonia [description not available] | 0 | 4.74 | 11 | 0 |
Pneumonia, Staphylococcal Pneumonia caused by infections with bacteria of the genus STAPHYLOCOCCUS, usually with STAPHYLOCOCCUS AUREUS. | 0 | 4.74 | 11 | 0 |
Occupational Injuries Injuries sustained from incidents in the course of work-related activities. | 0 | 2.81 | 3 | 0 |
Taste Disorder, Anterior Tongue [description not available] | 0 | 5.08 | 10 | 0 |
Spider Veins [description not available] | 0 | 7.37 | 24 | 2 |
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 | 7.37 | 24 | 2 |
Acromegaly Due To Pituitary Adenoma [description not available] | 0 | 4.15 | 5 | 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 | 10.16 | 40 | 2 |
Glial Cell Tumors [description not available] | 0 | 6.66 | 39 | 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 | 6.66 | 39 | 0 |
Dysmyelopoietic Syndromes [description not available] | 0 | 2.25 | 1 | 0 |
Myelodysplastic Syndromes Clonal hematopoietic stem cell disorders characterized by dysplasia in one or more hematopoietic cell lineages. They predominantly affect patients over 60, are considered preleukemic conditions, and have high probability of transformation into ACUTE MYELOID LEUKEMIA. | 0 | 2.25 | 1 | 0 |
Infectious Skin Diseases [description not available] | 0 | 4.75 | 12 | 0 |
Skin Diseases, Infectious Skin diseases caused by bacteria, fungi, parasites, or viruses. | 0 | 4.75 | 12 | 0 |
Leprosy, Cutaneous [description not available] | 0 | 3.51 | 8 | 0 |
Emesis, Postoperative [description not available] | 0 | 8.78 | 8 | 6 |
Postoperative Nausea and Vomiting Emesis and queasiness occurring after anesthesia. | 0 | 8.78 | 8 | 6 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 8.63 | 46 | 1 |
Asymptomatic Colonization [description not available] | 0 | 6.24 | 18 | 0 |
Cancer of Maxillary Sinus [description not available] | 0 | 6 | 27 | 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 | 3.07 | 5 | 0 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 2.61 | 2 | 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 | 2.61 | 2 | 0 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 2.95 | 4 | 0 |
Gangrene Death and putrefaction of tissue usually due to a loss of blood supply. | 0 | 4.17 | 17 | 0 |
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 | 2.95 | 4 | 0 |
Craniocerebral Injuries [description not available] | 0 | 6.36 | 40 | 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 | 6.36 | 40 | 0 |
Stomatitis, Vesicular [description not available] | 0 | 2.25 | 1 | 0 |
Stillbirth The event that a FETUS is born dead or stillborn. | 0 | 3.89 | 4 | 0 |
Atresia, Biliary [description not available] | 0 | 2.25 | 1 | 0 |
Polysyndactyly [description not available] | 0 | 6.66 | 30 | 0 |
Cryptophthalmos with Other Malformations [description not available] | 0 | 2.52 | 2 | 0 |
Biliary Atresia Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually, biliary atresia is found in infants and accounts for one third of the neonatal cholestatic JAUNDICE. | 0 | 2.25 | 1 | 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 | 3.3 | 6 | 0 |
Neoplasms, Sebaceous Gland [description not available] | 0 | 3.24 | 6 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 5.65 | 18 | 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 | 5.65 | 18 | 0 |
Otitis Media, Purulent [description not available] | 0 | 2.46 | 2 | 0 |
Otitis Media, Suppurative Inflammation of the middle ear with purulent discharge. | 0 | 2.46 | 2 | 0 |
Inflammatory Pseudotumor [description not available] | 0 | 2.25 | 1 | 0 |
Granuloma, Plasma Cell A slow-growing benign pseudotumor in which plasma cells greatly outnumber the inflammatory cells. | 0 | 2.25 | 1 | 0 |
Colitis, Granulomatous [description not available] | 0 | 3.29 | 6 | 0 |
Anal Fistula [description not available] | 0 | 2.31 | 1 | 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 | 3.29 | 6 | 0 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 9.06 | 23 | 3 |
Infections, Lentivirus [description not available] | 0 | 2.25 | 1 | 0 |
Caprine Diseases [description not available] | 0 | 5.08 | 9 | 0 |
Salivary Gland Calculi Calculi occurring in a salivary gland. Most salivary gland calculi occur in the submandibular gland, but can also occur in the parotid gland and in the sublingual and minor salivary glands. | 0 | 2.67 | 3 | 0 |
Bronchiolitis, Viral An acute inflammatory disease of the lower RESPIRATORY TRACT, caused by paramyxoviruses, occurring primarily in infants and young children; the viruses most commonly implicated are PARAINFLUENZA VIRUS TYPE 3; RESPIRATORY SYNCYTIAL VIRUS, HUMAN; and METAPNEUMOVIRUS. | 0 | 6.03 | 6 | 1 |
Craniofacial Pain [description not available] | 0 | 8.07 | 20 | 1 |
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 | 8.07 | 20 | 1 |
Beuren Syndrome [description not available] | 0 | 2.53 | 2 | 0 |
Body Rocking [description not available] | 0 | 3.86 | 2 | 1 |
Brain Inflammation [description not available] | 0 | 3.59 | 9 | 0 |
Chronic Lymphocytic Thyroiditis [description not available] | 0 | 2.51 | 2 | 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 | 3.59 | 9 | 0 |
Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | 0 | 2.51 | 2 | 0 |
Maxillary Fractures Fractures of the upper jaw. | 0 | 6.91 | 70 | 0 |
Intertrigo A superficial dermatitis occurring on skin surfaces in contact with each other, such as the axillae, neck creases, intergluteal fold, between the toes, etc. Obesity is a predisposing factor. The condition is caused by moisture and friction and is characterized by erythema, maceration, burning, and exudation. | 0 | 3.64 | 1 | 1 |
Clostridioides difficile Infection [description not available] | 0 | 2.77 | 3 | 0 |
Clostridium Infections Infections with bacteria of the genus CLOSTRIDIUM and closely related CLOSTRIDIOIDES species. | 0 | 2.77 | 3 | 0 |
Salmonella Infections, Animal Infections in animals with bacteria of the genus SALMONELLA. | 0 | 3.58 | 9 | 0 |
Infections, Respirovirus [description not available] | 0 | 5.62 | 18 | 1 |
Lung Adenocarcinoma [description not available] | 0 | 2.25 | 1 | 0 |
Cancer of Mouth [description not available] | 0 | 8.46 | 32 | 1 |
Ankylosing Spondylarthritis [description not available] | 0 | 2.78 | 3 | 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 | 2.25 | 1 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 8.46 | 32 | 1 |
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 | 2.78 | 3 | 0 |
Bacterial Eye Infections [description not available] | 0 | 6.36 | 10 | 0 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 1 | 6.52 | 9 | 0 |
Neoplasms, Sweat Gland [description not available] | 0 | 6 | 17 | 0 |
Eccrine Porocarcinoma A rare malignant neoplasm of the sweat glands. It most often develops as a form of degenerative progression from a benign ECCRINE POROMA. | 0 | 2.25 | 1 | 0 |
Absence of Corpus Callosum [description not available] | 0 | 6.1 | 13 | 0 |
47,XX,+21 [description not available] | 0 | 5.65 | 30 | 0 |
Agenesis of Corpus Callosum with Chorioretinal Abnormality [description not available] | 0 | 2.25 | 1 | 0 |
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 | 5.65 | 30 | 0 |
Infections, Paramyxoviridae [description not available] | 0 | 4.77 | 32 | 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 | 4.77 | 32 | 0 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 2.25 | 1 | 0 |
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 | 2.25 | 1 | 0 |
Acute Hepatic Failure [description not available] | 0 | 2.52 | 2 | 0 |
Liver Failure, Acute A form of rapid-onset LIVER FAILURE, also known as fulminant hepatic failure, caused by severe liver injury or massive loss of HEPATOCYTES. It is characterized by sudden development of liver dysfunction and JAUNDICE. Acute liver failure may progress to exhibit cerebral dysfunction even HEPATIC COMA depending on the etiology that includes hepatic ISCHEMIA, drug toxicity, malignant infiltration, and viral hepatitis such as post-transfusion HEPATITIS B and HEPATITIS C. | 0 | 2.52 | 2 | 0 |
Airway Remodeling The structural changes in the number, mass, size and/or composition of the airway tissues. | 0 | 3.77 | 3 | 0 |
Polychondritis, Chronic Atrophic [description not available] | 0 | 8.56 | 28 | 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 | 8.56 | 28 | 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 | 7.17 | 33 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 5.26 | 12 | 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 | 5.26 | 12 | 0 |
Abscess, Peritonsillar [description not available] | 0 | 2.89 | 4 | 0 |
Congenital Familial Lymphedema [description not available] | 0 | 3.97 | 5 | 0 |
Lymphedema Edema due to obstruction of lymph vessels or disorders of the lymph nodes. | 0 | 3.97 | 5 | 0 |
Acoustic Trauma Usually refer to hearing loss due to a single noise event such as an explosion or shotgun blast. | 0 | 3.39 | 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 | 3.39 | 2 | 0 |
Adnexal and Skin Appendage Neoplasms [description not available] | 0 | 2.48 | 2 | 0 |
Follicular Cyst Cyst due to the occlusion of the duct of a follicle or small gland. | 0 | 2.25 | 1 | 0 |
Basal Cell Cancer [description not available] | 0 | 2.46 | 2 | 0 |
Acne Rosacea [description not available] | 0 | 8.17 | 44 | 1 |
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 | 8.17 | 44 | 1 |
Ascaridida Infections Infections with nematodes of the order ASCARIDIDA. | 0 | 2.25 | 1 | 0 |
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 | 6.99 | 41 | 0 |
Hypertelorism Abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid. | 0 | 8.94 | 101 | 0 |
Chloasma [description not available] | 0 | 2.25 | 1 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 2.25 | 1 | 0 |
Lymphocytopenia [description not available] | 0 | 2.9 | 4 | 0 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 2.9 | 4 | 0 |
Sicca Syndrome [description not available] | 0 | 3.8 | 4 | 0 |
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 | 3.8 | 4 | 0 |
Sexually Transmitted Diseases Diseases due to or propagated by sexual contact. | 0 | 2.31 | 1 | 0 |
HIV Coinfection [description not available] | 0 | 4.68 | 26 | 0 |
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 | 4.68 | 26 | 0 |
Leucocythaemia [description not available] | 0 | 3.97 | 14 | 0 |
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 | 3.97 | 14 | 0 |
Dysostoses Defective bone formation involving individual bones, singly or in combination. | 0 | 4.66 | 6 | 0 |
Alopecia Circumscripta [description not available] | 0 | 2.38 | 2 | 0 |
Nail Diseases Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. | 0 | 2.45 | 2 | 0 |
Alopecia Areata Loss of scalp and body hair involving microscopically inflammatory patchy areas. | 0 | 2.38 | 2 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 5.64 | 18 | 0 |
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 | 5.64 | 18 | 0 |
Keratitis Inflammation of the cornea. | 0 | 3.8 | 4 | 0 |
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 | 4.69 | 6 | 0 |
Hives [description not available] | 0 | 4.8 | 5 | 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 | 4.8 | 5 | 0 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 3.84 | 4 | 0 |
Angiitis [description not available] | 0 | 4.93 | 8 | 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 | 3.84 | 4 | 0 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 4.93 | 8 | 0 |
Systemic Vasculitis A heterogeneous group of diseases characterized by inflammation and necrosis of the blood vessel walls. | 0 | 3.23 | 1 | 0 |
Adverse Effects, Long Term [description not available] | 0 | 2.63 | 2 | 0 |
Circoviridae Infections Virus diseases caused by the CIRCOVIRIDAE. | 0 | 3.31 | 6 | 0 |
Acute Ischemic Stroke [description not available] | 0 | 2.25 | 1 | 0 |
Hemorrhagic Stroke Stroke due to rupture of a weakened blood vessel in the brain (e.g., CEREBRAL HEMISPHERES; CEREBELLUM; SUBARACHNOID SPACE). | 0 | 2.25 | 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 | 2.25 | 1 | 0 |
Cancer Syndromes, Hereditary [description not available] | 0 | 3.44 | 8 | 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 | 6.41 | 42 | 1 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 2.25 | 1 | 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 | 2.25 | 1 | 0 |
Bullous Dermatoses [description not available] | 0 | 3.14 | 5 | 0 |
Herpes Zoster, Ocular [description not available] | 0 | 3.4 | 7 | 0 |
Skin Diseases, Viral Skin diseases caused by viruses. | 0 | 2.44 | 2 | 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 | 3.4 | 7 | 0 |
Hidrocystoma A cystic form of sweat gland adenoma (ADENOMA, SWEAT GLAND). It is produced by the cystic proliferation of apocrine secretory glands. It is not uncommon, occurring in adult life in no particular age group, with males and females equally affected. The commonest site is around the eye, particularly lateral to the outer canthus. It is cured by surgical removal. (Stedman, 25th ed; Rook et al., Textbook of Dermatology, 4th ed, p2410) | 0 | 4.73 | 6 | 0 |
Aneuploid [description not available] | 0 | 4.03 | 5 | 0 |
Aura [description not available] | 0 | 4.17 | 17 | 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 | 4.17 | 17 | 0 |
Pyoderma Any purulent skin disease (Dorland, 27th ed). | 0 | 3.67 | 10 | 0 |
Bovine Respiratory Disease Complex A multifactorial disease of CATTLE resulting from complex interactions between environmental factors, host factors, and pathogens. The environmental factors act as stressors adversely affecting the IMMUNE SYSTEM and other host defenses and enhancing transmission of infecting agents. | 0 | 2.85 | 3 | 0 |
Travel Sickness [description not available] | 0 | 2.31 | 1 | 0 |
Child Development Deviations [description not available] | 0 | 6.4 | 18 | 0 |
Eye Abnormalities Congenital absence of or defects in structures of the eye; may also be hereditary. | 0 | 8.86 | 102 | 0 |
Decreased Muscle Tone [description not available] | 0 | 3.39 | 7 | 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 | 6.4 | 18 | 0 |
Animal Diseases Diseases that occur in VERTEBRATE animals. | 0 | 3.23 | 6 | 0 |
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 | 5.48 | 25 | 0 |
Graft-Versus-Host Disease [description not available] | 0 | 2.31 | 1 | 0 |
Congenital Thrombotic Thrombocytopenic Purpura [description not available] | 0 | 2.61 | 2 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 3.79 | 11 | 0 |
Purpura Fulminans A severe, rapidly fatal reaction occurring most commonly in children following an infectious illness. It is characterized by large, rapidly spreading skin hemorrhages, fever, or shock. Purpura fulminans often accompanies or is triggered by DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 3.03 | 4 | 0 |
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 | 2.31 | 1 | 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 | 2.61 | 2 | 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 | 3.79 | 11 | 0 |
Cardiomyopathy, Congestive [description not available] | 0 | 2.31 | 1 | 0 |
Out-of-Hospital Cardiac Arrest Occurrence of heart arrest in an individual when there is no immediate access to medical personnel or equipment. | 0 | 2.53 | 2 | 0 |
Cardiomyopathy, Dilated A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein. | 0 | 2.31 | 1 | 0 |
Keratosis Seborrheica [description not available] | 0 | 2.31 | 1 | 0 |
Keratosis, Seborrheic Benign eccrine poromas that present as multiple oval, brown-to-black plaques, located mostly on the chest and back. The age of onset is usually in the fourth or fifth decade. | 0 | 2.31 | 1 | 0 |
Ebola Hemorrhagic Fever [description not available] | 0 | 2.66 | 2 | 0 |
Hemorrhagic Fever, Ebola A highly fatal, acute hemorrhagic fever caused by EBOLAVIRUS. | 0 | 2.66 | 2 | 0 |
Nevoxanthoendothelioma [description not available] | 0 | 2.31 | 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 | 2.88 | 4 | 0 |
Fibroma, Ossifying A benign central bone tumor, usually of the jaws (especially the mandible), composed of fibrous connective tissue within which bone is formed. | 0 | 3.48 | 7 | 0 |
Carcinoma, Basosquamous A skin carcinoma that histologically exhibits both basal and squamous elements. (From Dorland, 27th ed) | 0 | 3.09 | 5 | 0 |
Apoplexy [description not available] | 0 | 6.45 | 15 | 0 |
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 | 6.45 | 15 | 0 |
Pyrexia [description not available] | 0 | 7.13 | 34 | 3 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 7.13 | 34 | 3 |
Eczema, Atopic [description not available] | 0 | 8.28 | 26 | 2 |
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 | 8.28 | 26 | 2 |
Infusion Site Adverse Event [description not available] | 0 | 2.31 | 1 | 0 |
Blood Poisoning [description not available] | 0 | 10.1 | 56 | 2 |
Infections, Staphylococcal Skin [description not available] | 0 | 12.49 | 54 | 7 |
Staphylococcal Skin Infections Infections to the skin caused by bacteria of the genus STAPHYLOCOCCUS. | 0 | 12.49 | 54 | 7 |
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 | 10.1 | 56 | 2 |
Globus Hystericus [description not available] | 0 | 2.31 | 1 | 0 |
Injuries, Soft Tissue [description not available] | 0 | 8.62 | 25 | 1 |
Dermatitis, Eczematous [description not available] | 0 | 6.82 | 15 | 1 |
Eczema A pruritic papulovesicular dermatitis occurring as a reaction to many endogenous and exogenous agents (Dorland, 27th ed). | 0 | 6.82 | 15 | 1 |
Carcinoma, Neuroendocrine A group of carcinomas which share a characteristic morphology, often being composed of clusters and trabecular sheets of round blue cells, granular chromatin, and an attenuated rim of poorly demarcated cytoplasm. Neuroendocrine tumors include carcinoids, small (oat) cell carcinomas, medullary carcinoma of the thyroid, Merkel cell tumor, cutaneous neuroendocrine carcinoma, pancreatic islet cell tumors, and pheochromocytoma. Neurosecretory granules are found within the tumor cells. (Segen, Dictionary of Modern Medicine, 1992) | 0 | 3.98 | 4 | 0 |
Central Nervous System Neoplasm [description not available] | 0 | 2.95 | 4 | 0 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 2.95 | 4 | 0 |
Cholecystoduodenal Fistula [description not available] | 0 | 2.41 | 1 | 0 |
Cranial Nerve V Diseases [description not available] | 0 | 5.07 | 15 | 0 |
Dorsolateral Medullary Syndrome [description not available] | 0 | 3.25 | 6 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 9.73 | 33 | 1 |
Cancer of Esophagus [description not available] | 0 | 3.32 | 6 | 0 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 9.73 | 33 | 1 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 3.32 | 6 | 0 |
Cervical Tuberculous Lymphadenitis [description not available] | 0 | 2.87 | 4 | 0 |
Epiphora [description not available] | 0 | 6 | 27 | 0 |
Lacrimal Apparatus Diseases Diseases of the LACRIMAL APPARATUS. | 0 | 6 | 27 | 0 |
Synkinesis An involuntary movement accompanying a volitional movement. It often refers to facial movements that accompany FACIAL PARALYSIS. | 0 | 3.42 | 6 | 0 |
Anemias, Iron-Deficiency [description not available] | 0 | 5.18 | 4 | 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 | 5.18 | 4 | 0 |
Cutis Elastica [description not available] | 0 | 2.31 | 1 | 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 | 2.31 | 1 | 0 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 3.22 | 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 | 3.22 | 5 | 0 |
Encephalopathy, Traumatic [description not available] | 0 | 3.51 | 2 | 0 |
Enterocele An intestinal HERNIA. | 0 | 2.31 | 1 | 0 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 3.51 | 2 | 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 | 2.31 | 1 | 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 | 8.41 | 45 | 1 |
EBV Infections [description not available] | 0 | 3.22 | 5 | 0 |
B-Cell Lymphoma [description not available] | 0 | 2.47 | 2 | 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 | 2.47 | 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 | 3.22 | 5 | 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 | 3.9 | 13 | 0 |
Lacerations Torn, ragged, mangled wounds. | 0 | 7.28 | 16 | 1 |
Mucocele A retention cyst of the salivary gland, lacrimal sac, paranasal sinuses, appendix, or gallbladder. (Stedman, 26th ed) | 0 | 4.68 | 29 | 0 |
Hypothermia, Accidental [description not available] | 0 | 2.65 | 3 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 2.65 | 3 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 2.38 | 2 | 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 | 2.38 | 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 | 3.63 | 9 | 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 | 2.46 | 2 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 3.61 | 9 | 0 |
Microbial Superinvasion [description not available] | 0 | 5.44 | 5 | 1 |
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 | 3.61 | 9 | 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 | 3.39 | 7 | 0 |
Disease, Pulmonary [description not available] | 0 | 16.9 | 289 | 4 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 16.9 | 289 | 4 |
Zygomatic Fractures Fractures of the zygoma. | 0 | 6.98 | 54 | 0 |
Parasite Infections [description not available] | 0 | 4.62 | 6 | 1 |
Amblyopia, Developmental [description not available] | 0 | 2.15 | 1 | 0 |
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 | 2.15 | 1 | 0 |
Burns, Chemical Burns caused by contact with or exposure to CAUSTICS or strong ACIDS. | 0 | 5.41 | 10 | 0 |
Injuries, Teeth [description not available] | 0 | 4.42 | 8 | 0 |
Cranial Nerve II Injuries [description not available] | 0 | 5.35 | 13 | 0 |
Cranial Nerve I Diseases [description not available] | 0 | 2.15 | 1 | 0 |
Adhesions, Tissue [description not available] | 0 | 7.29 | 22 | 2 |
Ozena [description not available] | 0 | 9.14 | 92 | 0 |
Sinusitis, Sphenoid [description not available] | 0 | 4.01 | 5 | 0 |
Rhinitis, Atrophic A chronic inflammation in which the NASAL MUCOSA gradually changes from a functional to a non-functional lining without mucociliary clearance. It is often accompanied by degradation of the bony TURBINATES, and the foul-smelling mucus which forms a greenish crust (ozena). | 0 | 9.14 | 92 | 0 |
Lupus Erythematosus, Cutaneous, Subacute [description not available] | 0 | 3.25 | 6 | 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 | 3.25 | 6 | 0 |
Anosmic Hypogonadism [description not available] | 0 | 2.91 | 4 | 0 |
Kallmann Syndrome A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait. | 0 | 2.91 | 4 | 0 |
Cerebral Concussion [description not available] | 0 | 3.3 | 2 | 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 | 3.3 | 2 | 0 |
Bacterial Infections, Gram-Negative [description not available] | 0 | 3.32 | 6 | 0 |
Gram-Negative Bacterial Infections Infections caused by bacteria that show up as pink (negative) when treated by the gram-staining method. | 0 | 3.32 | 6 | 0 |
Infections, Prosthesis-Related [description not available] | 0 | 6.65 | 14 | 0 |
Atypical Mycobacterial Infection, Disseminated [description not available] | 0 | 3.42 | 7 | 0 |
Infections, Serratia [description not available] | 0 | 3.3 | 6 | 0 |
Arteriosclerosis, Coronary [description not available] | 0 | 3.56 | 1 | 1 |
Diaphragmatic Paralysis [description not available] | 0 | 5.67 | 7 | 1 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 3.56 | 1 | 1 |
Fractures, Comminuted A fracture in which the bone is splintered or crushed into a number of pieces. | 0 | 4.44 | 8 | 0 |
Mandibular Fractures Fractures of the lower jaw. | 0 | 7.4 | 53 | 0 |
Long Sleeper Syndrome [description not available] | 0 | 8.46 | 12 | 3 |
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 | 8.46 | 12 | 3 |
Familial Nonmedullary Thyroid Cancer [description not available] | 0 | 2.52 | 2 | 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 | 3.07 | 5 | 0 |
Dehiscence, Surgical Wound [description not available] | 0 | 4.32 | 7 | 0 |
Amyotonia Congenita [description not available] | 0 | 6.65 | 11 | 2 |
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 | 6.65 | 11 | 2 |
Anodontia Congenital absence of the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the deciduous and the permanent dentition, or only teeth of the permanent dentition. (Dorland, 27th ed) | 0 | 4.47 | 22 | 0 |
Sinusitis, Maxillary [description not available] | 0 | 8.13 | 32 | 2 |
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 | 8.13 | 32 | 2 |
Lock Jaw [description not available] | 0 | 2.9 | 4 | 0 |
Hypoventilation A reduction in the amount of air entering the pulmonary alveoli. | 0 | 4.28 | 7 | 0 |
Pulmonary Hypertension [description not available] | 0 | 5.22 | 4 | 1 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 5.22 | 4 | 1 |
Tooth Diseases Diseases involving the TEETH. | 0 | 3.11 | 5 | 0 |
Congenital X-Linked Retinoschisis [description not available] | 0 | 2.15 | 1 | 0 |
Gender Dysphoria A marked difference between the individual’s expressed/experienced gender and the gender others would assign to the individual, and it must continue for at least six months. (from DSM-5) | 0 | 3.5 | 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 | 2.15 | 1 | 0 |
Behavior Disorder, Rapid Eye Movement Sleep [description not available] | 0 | 3.09 | 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 | 3.09 | 1 | 0 |
Pallor A clinical manifestation consisting of an unnatural paleness of the skin. | 0 | 2.51 | 2 | 0 |
Infections, Soft Tissue [description not available] | 0 | 9.97 | 23 | 5 |
Soft Tissue Infections Infections of non-skeletal tissue, i.e., exclusive of bone, ligaments, cartilage, and fibrous tissue. The concept is usually referred to as skin and soft tissue infections and usually subcutaneous and muscle tissue are involved. The predisposing factors in anaerobic infections are trauma, ischemia, and surgery. The organisms often derive from the fecal or oral flora, particularly in wounds associated with intestinal surgery, decubitus ulcer, and human bites. (From Cecil Textbook of Medicine, 19th ed, p1688) | 0 | 9.97 | 23 | 5 |
Neoplasms, Vascular [description not available] | 0 | 2.82 | 3 | 0 |
Complications, Infectious Pregnancy [description not available] | 0 | 7.27 | 24 | 1 |
Bordetella pertussis Infection, Respiratory [description not available] | 0 | 5.52 | 16 | 1 |
Whooping Cough A respiratory infection caused by BORDETELLA PERTUSSIS and characterized by paroxysmal coughing ending in a prolonged crowing intake of breath. | 0 | 5.52 | 16 | 1 |
Preterm Birth [description not available] | 0 | 3.01 | 4 | 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 | 3.01 | 4 | 0 |
Malnourishment [description not available] | 0 | 3.23 | 6 | 0 |
Malnutrition An imbalanced nutritional status resulting from insufficient intake of nutrients to meet normal physiological requirement. | 0 | 3.23 | 6 | 0 |
Infectious Diseases [description not available] | 0 | 5.47 | 16 | 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 | 5.47 | 16 | 0 |
Chondromalacia of Trachea and Bronchi [description not available] | 0 | 2.5 | 2 | 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 | 4.25 | 6 | 0 |
Aesthesioneuroblastoma [description not available] | 0 | 5.47 | 10 | 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 | 5.47 | 10 | 0 |
Oroantral Fistula A fistula between the maxillary sinus and the oral cavity. | 0 | 3.37 | 7 | 0 |
Diseases of Nasopharynx [description not available] | 0 | 6.05 | 29 | 0 |
Angiospasm, Intracranial [description not available] | 0 | 4.21 | 3 | 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 | 4.21 | 3 | 0 |
Coccidioides immitis Infection [description not available] | 0 | 4.03 | 5 | 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 | 4.03 | 5 | 0 |
Hypesthesia Absent or reduced sensitivity to cutaneous stimulation. | 0 | 4.65 | 10 | 0 |
Debility [description not available] | 0 | 2.15 | 1 | 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 | 5.6 | 30 | 0 |
Cutaneous T-Cell Lymphoma [description not available] | 0 | 2.78 | 3 | 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 | 2.78 | 3 | 0 |
Bisphosphonate Osteonecrosis [description not available] | 0 | 2.17 | 1 | 0 |
Inhalation Injury, Smoke [description not available] | 0 | 2.94 | 4 | 0 |
Burns, Inhalation Burns of the respiratory tract caused by heat or inhaled chemicals. | 0 | 2.7 | 3 | 0 |
Tachypnea Increased RESPIRATORY RATE. | 0 | 2.17 | 1 | 0 |
Abnormality, Heart [description not available] | 0 | 7.26 | 33 | 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 | 7.26 | 33 | 0 |
Vesicoureteral Reflux [description not available] | 0 | 2.15 | 1 | 0 |
Hypotrichosis Presence of less than the normal amount of hair. (Dorland, 27th ed) | 0 | 4.68 | 11 | 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 | 2.15 | 1 | 0 |
Atheroma [description not available] | 0 | 3.09 | 1 | 0 |
Cancer of Larynx [description not available] | 0 | 6.75 | 14 | 1 |
Lymph Node Metastasis [description not available] | 0 | 5.66 | 19 | 0 |
Angiogranuloma [description not available] | 0 | 3.6 | 3 | 0 |
Laryngeal Neoplasms Cancers or tumors of the LARYNX or any of its parts: the GLOTTIS; EPIGLOTTIS; LARYNGEAL CARTILAGES; LARYNGEAL MUSCLES; and VOCAL CORDS. | 0 | 6.75 | 14 | 1 |
Blood Pressure, High [description not available] | 0 | 11.71 | 29 | 10 |
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 | 11.71 | 29 | 10 |
Allergic Contact Dermatitis [description not available] | 0 | 4.8 | 7 | 1 |
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 | 4.8 | 7 | 1 |
Hypomelanosis [description not available] | 0 | 2.52 | 2 | 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 | 2.52 | 2 | 0 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 2.44 | 2 | 0 |
Constipation Infrequent or difficult evacuation of FECES. These symptoms are associated with a variety of causes, including low DIETARY FIBER intake, emotional or nervous disturbances, systemic and structural disorders, drug-induced aggravation, and infections. | 0 | 2.44 | 2 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 9.52 | 32 | 1 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 9.52 | 32 | 1 |
Black Fever [description not available] | 0 | 3.41 | 7 | 0 |
Enlarged Spleen [description not available] | 0 | 2.38 | 2 | 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 | 3.41 | 7 | 0 |
Bradyarrhythmia [description not available] | 0 | 3.22 | 6 | 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 | 3.22 | 6 | 0 |
Dermatomyositis, Adult Type [description not available] | 0 | 2.53 | 2 | 0 |
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 | 2.53 | 2 | 0 |
Communicable Diseases, Emerging Infectious diseases that are novel in their outbreak ranges (geographic and host) or transmission mode. | 0 | 3.37 | 6 | 0 |
Atresia, Esophageal [description not available] | 0 | 4.16 | 6 | 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 | 4.16 | 6 | 0 |
Genital Warts [description not available] | 0 | 2.36 | 2 | 0 |
Condylomata Acuminata Sexually transmitted form of anogenital warty growth caused by the human papillomaviruses. | 0 | 2.36 | 2 | 0 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 11.62 | 110 | 2 |
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 | 11.62 | 110 | 2 |
Addiction, Opioid [description not available] | 0 | 3.44 | 2 | 0 |
Opioid-Related Disorders Disorders related to or resulting from abuse or misuse of OPIOIDS. | 0 | 3.44 | 2 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial [description not available] | 0 | 2.21 | 1 | 0 |
Lymphohistiocytosis, Hemophagocytic A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 2.21 | 1 | 0 |
Adenocarcinoma, Papillary An adenocarcinoma containing finger-like processes of vascular connective tissue covered by neoplastic epithelium, projecting into cysts or the cavity of glands or follicles. It occurs most frequently in the ovary and thyroid gland. (Stedman, 25th ed) | 0 | 2.87 | 4 | 0 |
Central Nervous System Disease [description not available] | 0 | 4.27 | 7 | 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 | 4.27 | 7 | 0 |
HPV Infection [description not available] | 0 | 2.72 | 3 | 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 | 2.72 | 3 | 0 |
Complications of Diabetes Mellitus [description not available] | 0 | 6.68 | 21 | 1 |
Neoplasms, Skull [description not available] | 0 | 5.91 | 25 | 0 |
Agitation, Psychomotor [description not available] | 0 | 4.44 | 2 | 2 |
Psychomotor Agitation A feeling of restlessness associated with increased motor activity. This may occur as a manifestation of nervous system drug toxicity or other conditions. | 0 | 4.44 | 2 | 2 |
Allergic Angiitis [description not available] | 0 | 3.38 | 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 | 3.38 | 2 | 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 | 6.04 | 20 | 0 |
Parakeratosis Persistence of the nuclei of the keratinocytes into the stratum corneum of the skin. This is a normal state only in the epithelium of true mucous membranes in the mouth and vagina. (Dorland, 27th ed) | 0 | 2.96 | 4 | 0 |
Prognathism A condition marked by abnormal protrusion of the mandible. (Dorland, 27th ed) | 0 | 8.05 | 53 | 1 |
Active Hyperemia [description not available] | 0 | 3.43 | 7 | 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 | 3.43 | 7 | 0 |
Genetic Predisposition [description not available] | 0 | 5.36 | 21 | 0 |
Dry Eye [description not available] | 0 | 5.33 | 7 | 0 |
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 | 5.33 | 7 | 0 |
Autoimmune Disease [description not available] | 0 | 4.17 | 6 | 0 |
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 | 4.17 | 6 | 0 |
Disseminated Fusariosis [description not available] | 0 | 2.17 | 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 | 2.17 | 1 | 0 |
Injuries, Maxillofacial [description not available] | 0 | 8.63 | 89 | 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 | 5.45 | 15 | 0 |
Transmissible Venereal Tumors [description not available] | 0 | 2.17 | 1 | 0 |
Bruise [description not available] | 0 | 4.45 | 8 | 0 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 4.45 | 8 | 0 |
Cephalgia Syndromes [description not available] | 0 | 3.89 | 2 | 1 |
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 | 3.89 | 2 | 1 |
Encephalitis, West Nile Fever [description not available] | 0 | 2.55 | 2 | 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 | 2.55 | 2 | 0 |
Chromosome Deletion Actual loss of portion of a chromosome. | 0 | 6.73 | 32 | 0 |
Bleeding [description not available] | 0 | 11.92 | 106 | 6 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 11.92 | 106 | 6 |
Neoplasm Regression, Spontaneous Disappearance of a neoplasm or neoplastic state without the intervention of therapy. | 0 | 2.17 | 1 | 0 |
Merkel Cell Cancer [description not available] | 0 | 5.3 | 12 | 0 |
Multiple Primary Neoplasms [description not available] | 0 | 5.49 | 11 | 0 |
Carcinoma, Merkel Cell A carcinoma arising from MERKEL CELLS located in the basal layer of the epidermis and occurring most commonly as a primary neuroendocrine carcinoma of the skin. Merkel cells are tactile cells of neuroectodermal origin and histologically show neurosecretory granules. The skin of the head and neck are a common site of Merkel cell carcinoma, occurring generally in elderly patients. (Holland et al., Cancer Medicine, 3d ed, p1245) | 0 | 5.3 | 12 | 0 |
Injuries, Eye [description not available] | 0 | 5.98 | 27 | 0 |
Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | 0 | 5.98 | 27 | 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 | 8.06 | 21 | 2 |
Cancer of Salivary Gland [description not available] | 0 | 2.87 | 4 | 0 |
Foreign-Body Granuloma [description not available] | 0 | 3.76 | 10 | 0 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 2.87 | 4 | 0 |
Cardiac Diseases [description not available] | 0 | 4.42 | 8 | 0 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 4.42 | 8 | 0 |
Pilonidal Cyst [description not available] | 0 | 2.91 | 4 | 0 |
Pilonidal Sinus A hair-containing cyst or sinus, occurring chiefly in the coccygeal region. | 0 | 2.91 | 4 | 0 |
Tooth Eruption, Ectopic An abnormality in the direction of a TOOTH ERUPTION. | 0 | 4.18 | 17 | 0 |
Apocrine Poroma Benign adnexal neoplasm whose glandular secretion includes the release of part of the secreting cell. | 0 | 2.15 | 1 | 0 |
Calculosis [description not available] | 0 | 2.67 | 3 | 0 |
Palmoplantaris Pustulosis [description not available] | 0 | 4.76 | 7 | 1 |
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 | 4.76 | 7 | 1 |
Hyperekplexia A neurological disorder characterized by an excessive startle reaction with ABNORMAL REFLEX; MYOCLONIC JERKS; and MUSCLE HYPERTONIA. | 0 | 2.17 | 1 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 7.06 | 46 | 0 |
Cancer of Pharynx [description not available] | 0 | 4.99 | 16 | 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 | 7.06 | 46 | 0 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 0 | 4.99 | 16 | 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 | 3.85 | 12 | 0 |
Metastase [description not available] | 0 | 5.08 | 17 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 2.52 | 2 | 0 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 5.08 | 17 | 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 | 2.52 | 2 | 0 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 14.3 | 61 | 0 |
Abscess, Retropharyngeal [description not available] | 0 | 3.73 | 3 | 0 |
E coli Infections [description not available] | 0 | 3.36 | 7 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 3.36 | 7 | 0 |
Bowel Incontinence [description not available] | 0 | 2.21 | 1 | 0 |
Fecal Incontinence Failure of voluntary control of the anal sphincters, with involuntary passage of feces and flatus. | 0 | 2.21 | 1 | 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 | 2.21 | 1 | 0 |
Barotrauma Injury following pressure changes; includes injury to the eustachian tube, ear drum, lung and stomach. | 0 | 3.6 | 9 | 0 |
Mucopolysaccharidosis [description not available] | 0 | 2.48 | 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 | 2.48 | 2 | 0 |
Esophageal Reflux [description not available] | 0 | 10.19 | 24 | 3 |
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 | 10.19 | 24 | 3 |
Bacterial Meningitides [description not available] | 0 | 2.72 | 3 | 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 | 2.72 | 3 | 0 |
Acquired Vocal Cord Palsy [description not available] | 0 | 3 | 4 | 0 |
Vocal Cord Paralysis Congenital or acquired paralysis of one or both VOCAL CORDS. This condition is caused by defects in the CENTRAL NERVOUS SYSTEM, the VAGUS NERVE and branches of LARYNGEAL NERVES. Common symptoms are VOICE DISORDERS including HOARSENESS or APHONIA. | 0 | 3 | 4 | 0 |
Benign Supratentorial Neoplasms [description not available] | 0 | 2.17 | 1 | 0 |
Acute Necrotizing Encephalitis, Herpetic [description not available] | 0 | 2.52 | 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 | 2.52 | 2 | 0 |
Absence Seizure Disorder [description not available] | 0 | 2.17 | 1 | 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 | 2.17 | 1 | 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 | 2.31 | 1 | 0 |
Hyperplasia, Reactive Lymphoid [description not available] | 0 | 3.29 | 6 | 0 |
Sycosis [description not available] | 0 | 3.75 | 11 | 0 |
Folliculitis Inflammation of follicles, primarily hair follicles. | 0 | 3.75 | 11 | 0 |
Histiocytosis General term for the abnormal appearance of histiocytes in the blood. Based on the pathological features of the cells involved rather than on clinical findings, the histiocytic diseases are subdivided into three groups: HISTIOCYTOSIS, LANGERHANS CELL; HISTIOCYTOSIS, NON-LANGERHANS-CELL; and HISTIOCYTIC DISORDERS, MALIGNANT. | 0 | 2.21 | 1 | 0 |
Xanthoma [description not available] | 0 | 3.23 | 6 | 0 |
Abnormalities, Urogenital [description not available] | 0 | 2.69 | 3 | 0 |
Congenital Micrognathia [description not available] | 0 | 6.11 | 30 | 0 |
Infections, Plasmodium [description not available] | 0 | 2.17 | 1 | 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 | 2.17 | 1 | 0 |
Mastitis, Bovine INFLAMMATION of the UDDER in cows. | 0 | 3.22 | 6 | 0 |
Respiratory Tract Fistula An abnormal passage communicating between any component of the respiratory tract or between any part of the respiratory system and surrounding organs. | 0 | 3.92 | 12 | 0 |
Catheter-Associated Infections [description not available] | 0 | 3.05 | 4 | 0 |
22q11.2 Deletion Syndrome [description not available] | 0 | 2.72 | 3 | 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 | 2.72 | 3 | 0 |
Cold Sore [description not available] | 0 | 2.65 | 3 | 0 |
Herpes Simplex Keratitis [description not available] | 0 | 2.17 | 1 | 0 |
Herpes Labialis Herpes simplex, caused by type 1 virus, primarily spread by oral secretions and usually occurring as a concomitant of fever. It may also develop in the absence of fever or prior illness. It commonly involves the facial region, especially the lips and the nares. (Dorland, 27th ed.) | 0 | 2.65 | 3 | 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 | 2.17 | 1 | 0 |
Hansen Disease [description not available] | 0 | 6.8 | 63 | 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 | 6.8 | 63 | 0 |
Craniofacial Dysarthrosis [description not available] | 0 | 8.81 | 74 | 0 |
Regurgitation, Gastric GASTROESOPHAGEAL REFLUX wherein the retrograde flow passes through the UPPER ESOPHAGEAL SPHINCTER | 0 | 2.51 | 2 | 0 |
Laryngopharyngeal Reflux Back flow of gastric contents to the LARYNGOPHARYNX where it comes in contact with tissues of the upper aerodigestive tract. Laryngopharyngeal reflux is an extraesophageal manifestation of GASTROESOPHAGEAL REFLUX. | 0 | 2.51 | 2 | 0 |
Kahler Disease [description not available] | 0 | 4.58 | 10 | 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 | 4.58 | 10 | 0 |
Granulocytic Leukemia, Chronic [description not available] | 0 | 3.69 | 3 | 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 | 3.69 | 3 | 0 |
Hyperlipemia [description not available] | 0 | 2.21 | 1 | 0 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 2.21 | 1 | 0 |
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 | 5.43 | 5 | 1 |
Developmental Coordination Disorder [description not available] | 0 | 2.17 | 1 | 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 | 3.83 | 12 | 0 |
Bovine Virus Diarrhea Mucosal Disease [description not available] | 0 | 6.23 | 13 | 1 |
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 | 2.95 | 4 | 0 |
Dermatitis, Occupational A recurrent contact dermatitis caused by substances found in the work place. | 0 | 2.69 | 3 | 0 |
Avian Diseases [description not available] | 0 | 3.97 | 14 | 0 |
Bilharziasis [description not available] | 0 | 3.2 | 6 | 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 | 3.2 | 6 | 0 |
CHARGE Association [description not available] | 0 | 2.8 | 3 | 0 |
Blunt Injuries [description not available] | 0 | 5.52 | 16 | 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 | 2.49 | 2 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 3.25 | 6 | 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 | 3.25 | 6 | 0 |
Eardrum Perforation [description not available] | 0 | 4.81 | 2 | 1 |
Tympanic Membrane Perforation A temporary or persistent opening in the eardrum (TYMPANIC MEMBRANE). Clinical signs depend on the size, location, and associated pathological condition. | 0 | 4.81 | 2 | 1 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 2.51 | 2 | 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 | 2.51 | 2 | 0 |
Wounds, Penetrating Wounds caused by objects penetrating the skin. | 0 | 6.81 | 34 | 0 |
Injuries, Multiple [description not available] | 0 | 4.73 | 11 | 0 |
Fibromatosis [description not available] | 0 | 4.3 | 20 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 4.3 | 20 | 0 |
Allergic Conjunctivitis [description not available] | 0 | 3.42 | 2 | 0 |
Conjunctivitis, Allergic Conjunctivitis due to hypersensitivity to various allergens. | 0 | 3.42 | 2 | 0 |
Cerebral Nocardiosis [description not available] | 0 | 2.89 | 4 | 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 | 3.75 | 11 | 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 | 3.24 | 6 | 0 |
Abnormalities, Jaw [description not available] | 0 | 7.72 | 35 | 0 |
Cardiovascular Stroke [description not available] | 0 | 2.71 | 3 | 0 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 2.71 | 3 | 0 |
Acantholysis Separation of the prickle cells of the stratum spinosum of the epidermis, resulting in atrophy of the prickle cell layer. It is seen in diseases such as pemphigus vulgaris (see PEMPHIGUS) and DARIER DISEASE. | 0 | 2.21 | 1 | 0 |
Congenital Varicella Syndrome [description not available] | 0 | 2.21 | 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 | 2.78 | 3 | 0 |
Licheniform Eruptions [description not available] | 0 | 2.46 | 2 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 6.06 | 11 | 1 |
Carcinoma, Skin Appendage A malignant tumor of the skin appendages, which include the hair, nails, sebaceous glands, sweat glands, and the mammary glands. (From Dorland, 27th ed) | 0 | 4.53 | 5 | 0 |
Febrile Neutropenia Fever accompanied by a significant reduction in the number of NEUTROPHILS. | 0 | 2.21 | 1 | 0 |
Blood Clot [description not available] | 0 | 4.37 | 8 | 0 |
Extravasation of Contrast Media [description not available] | 0 | 3.46 | 2 | 0 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 4.37 | 8 | 0 |
Esophageal Hernia [description not available] | 0 | 2.98 | 4 | 0 |
ADDH [description not available] | 0 | 4.58 | 5 | 1 |
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 | 4.58 | 5 | 1 |
Ataxia Telangiectasia Syndrome [description not available] | 0 | 3.41 | 2 | 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 | 3.41 | 2 | 0 |
Diseases of Pharynx [description not available] | 0 | 7.81 | 70 | 1 |
Mediastinitis Inflammation of the mediastinum, the area between the pleural sacs. | 0 | 2.77 | 3 | 0 |
Lung Injury, Acute [description not available] | 0 | 4.21 | 3 | 0 |
Acute Lung Injury A condition of lung damage that is characterized by bilateral pulmonary infiltrates (PULMONARY EDEMA) rich in NEUTROPHILS, and in the absence of clinical HEART FAILURE. This can represent a spectrum of pulmonary lesions, endothelial and epithelial, due to numerous factors (physical, chemical, or biological). | 1 | 6.21 | 3 | 0 |
Muscular Dystrophy [description not available] | 0 | 6.01 | 10 | 1 |
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 | 6.01 | 10 | 1 |
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 | 3.02 | 4 | 0 |
Infections, Meningococcal [description not available] | 0 | 4.89 | 8 | 1 |
Meningococcal Infections Infections with bacteria of the species NEISSERIA MENINGITIDIS. | 0 | 4.89 | 8 | 1 |
Gouty Arthritis [description not available] | 0 | 3.12 | 1 | 0 |
Arthritis, Gouty Arthritis, especially of the great toe, as a result of gout. Acute gouty arthritis often is precipitated by trauma, infection, surgery, etc. The initial attacks are usually monoarticular but later attacks are often polyarticular. Acute and chronic gouty arthritis are associated with accumulation of MONOSODIUM URATE in and around affected joints. | 0 | 3.12 | 1 | 0 |
Celiac Sprue [description not available] | 0 | 3.31 | 2 | 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 | 3.31 | 2 | 0 |
Nevi, Melanocytic [description not available] | 0 | 5.64 | 19 | 1 |
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 | 5.64 | 19 | 1 |
Degenerative Disc Disease [description not available] | 0 | 2.21 | 1 | 0 |
Intervertebral Disc Degeneration Degenerative changes in the INTERVERTEBRAL DISC due to aging or structural damage, especially to the vertebral end-plates. | 0 | 2.21 | 1 | 0 |
Maxillary Diseases Diseases involving the MAXILLA. | 0 | 6.45 | 24 | 0 |
Chronic Kidney Failure [description not available] | 0 | 5.74 | 11 | 2 |
Primary Peritonitis [description not available] | 0 | 7.06 | 19 | 5 |
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 | 5.74 | 11 | 2 |
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 | 7.06 | 19 | 5 |
Abnormalities, Teeth [description not available] | 0 | 8.08 | 40 | 1 |
Nasopharyngitis Inflammation of the NASOPHARYNX, usually including its mucosa, related lymphoid structure, and glands. | 0 | 4.07 | 16 | 0 |
Anhidrotic Ectodermal Dysplasia, X-Linked [description not available] | 0 | 2.57 | 2 | 0 |
Ectodermal Dysplasia 1, Anhidrotic An X-linked form of ectodermal dysplasia which results from mutations of the gene encoding ECTODYSPLASIN. | 0 | 2.57 | 2 | 0 |
Munchausen Syndrome by Proxy A phenomenon in which symptoms of a disease are fabricated by an individual other than the patient causing unnecessary, and often painful, physical examinations and treatments. This syndrome is considered a form of CHILD ABUSE, since another individual, usually a parent, is the source of the fabrication of symptoms and presents the child for medical care. | 0 | 2.44 | 2 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 2.66 | 3 | 0 |
Colorectal Cancer [description not available] | 0 | 2.68 | 3 | 0 |
Intestinal Obstruction Any impairment, arrest, or reversal of the normal flow of INTESTINAL CONTENTS toward the ANAL CANAL. | 0 | 5.33 | 13 | 1 |
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 | 2.68 | 3 | 0 |
Agnosia for Faces [description not available] | 0 | 2.77 | 3 | 0 |
Myelomonocytic Leukemia, Chronic [description not available] | 0 | 2.21 | 1 | 0 |
Leukemia, Myelomonocytic, Chronic A myelodysplastic-myeloproliferative disease characterized by monocytosis, increased monocytes in the bone marrow, variable degrees of dysplasia, but an absence of immature granulocytes in the blood. | 0 | 2.21 | 1 | 0 |
Cicatrix, Hypertrophic An elevated scar, resembling a KELOID, but which does not spread into surrounding tissues. It is formed by enlargement and overgrowth of cicatricial tissue and regresses spontaneously. | 0 | 5.04 | 3 | 1 |
Arterial Obstructive Diseases [description not available] | 0 | 3.1 | 5 | 0 |
External Ophthalmoplegia [description not available] | 0 | 3.75 | 11 | 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 | 3.1 | 5 | 0 |
Eperythrozoonosis [description not available] | 0 | 5 | 41 | 0 |
Enzootic Pneumonia of Pigs [description not available] | 0 | 2.21 | 1 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 3.85 | 4 | 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 | 3.85 | 4 | 0 |
Angle Class I [description not available] | 0 | 6.97 | 39 | 0 |
Articulation Disorders Disorders of the quality of speech characterized by the substitution, omission, distortion, and addition of phonemes. | 0 | 5.46 | 15 | 0 |
Cervical Fusion Syndrome [description not available] | 0 | 2.89 | 4 | 0 |
Conus Medullaris Syndrome [description not available] | 0 | 4.97 | 8 | 0 |
Spinal Stenosis Narrowing of the spinal canal. | 0 | 2.5 | 2 | 0 |
Rubeola [description not available] | 0 | 3.2 | 6 | 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 | 3.2 | 6 | 0 |
Alcohol Related Neurodevelopmental Disorder [description not available] | 0 | 2.42 | 2 | 0 |
Clostridium tetani Infection [description not available] | 0 | 3.45 | 8 | 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 | 3.45 | 8 | 0 |
Wounds, Stab Penetrating wounds caused by a pointed object. | 0 | 4.15 | 6 | 0 |
Familial Precocious Puberty [description not available] | 0 | 2.21 | 1 | 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 | 2.21 | 1 | 0 |
P carinii Pneumonia [description not available] | 0 | 3.11 | 5 | 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 | 3.11 | 5 | 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 | 2.08 | 1 | 0 |
Congenital Limb Deformities [description not available] | 0 | 6.68 | 21 | 0 |
Aberrant Tissue [description not available] | 0 | 4.17 | 6 | 0 |
Thyroglossal Cyst A cyst in the neck caused by persistence of portions of, or by lack of closure of, the primitive thyroglossal duct. (Dorland, 27th ed) | 0 | 3 | 1 | 0 |
Scalp Dermatoses Skin diseases involving the SCALP. | 0 | 3.37 | 2 | 0 |
Infection, Wound [description not available] | 0 | 8.38 | 21 | 1 |
Bronchiectasis Persistent abnormal dilatation of the bronchi. | 0 | 8.35 | 16 | 2 |
Deafness-Retinitis Pigmentosa Syndrome [description not available] | 0 | 2.08 | 1 | 0 |
Empty Sella Syndrome A condition when the SELLA TURCICA is not filled with pituitary tissue. The pituitary gland is either compressed, atrophied, or removed. There are two types: (1) primary empty sella is due a defect in the sella diaphragm leading to arachnoid herniation into the sellar space; (2) secondary empty sella is associated with the removal or treatment of PITUITARY NEOPLASMS. | 0 | 2.49 | 2 | 0 |
Vasomotor Rhinitis [description not available] | 0 | 8.6 | 30 | 2 |
Rhinitis, Vasomotor A form of non-allergic rhinitis that is characterized by nasal congestion and posterior pharyngeal drainage. | 1 | 10.6 | 30 | 2 |
Pneumopericardium Presence of air or gas in the space between the heart and the PERICARDIUM. The degree of respiratory distress depends on the amount of trapped air and circulation blocked in the systemic and pulmonary veins. | 0 | 2.07 | 1 | 0 |
Alagille Syndrome 1 [description not available] | 0 | 2.1 | 1 | 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 | 2.1 | 1 | 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 | 6.08 | 11 | 1 |
Temporomandibular Disorders [description not available] | 0 | 4.45 | 8 | 0 |
Temporomandibular Joint Disorders A variety of conditions affecting the anatomic and functional characteristics of the temporomandibular joint. Factors contributing to the complexity of temporomandibular diseases are its relation to dentition and mastication and the symptomatic effects in other areas which account for referred pain to the joint and the difficulties in applying traditional diagnostic procedures to temporomandibular joint pathology where tissue is rarely obtained and x-rays are often inadequate or nonspecific. Common diseases are developmental abnormalities, trauma, subluxation, luxation, arthritis, and neoplasia. (From Thoma's Oral Pathology, 6th ed, pp577-600) | 0 | 4.45 | 8 | 0 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 5.44 | 5 | 1 |
Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | 0 | 5.44 | 5 | 1 |
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 | 2.08 | 1 | 0 |
Disseminated Superficial Actinic Porokeratosis [description not available] | 0 | 3.67 | 3 | 0 |
Porokeratosis A heritable disorder of faulty keratinization characterized by the proliferation of abnormal clones of KERATINOCYTES and lesions showing varying atrophic patches surrounded by an elevated, keratotic border. These keratotic lesions can progress to overt cutaneous neoplasm. Several clinical variants are recognized, including porokeratosis of Mibelli, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis, and punctate porokeratosis. | 0 | 3.67 | 3 | 0 |
Injuries, Mandibular [description not available] | 0 | 4.9 | 14 | 0 |
Distorted Hearing [description not available] | 0 | 7.46 | 30 | 1 |
Franceschetti-Zwahlen-Klein Syndrome [description not available] | 0 | 5.49 | 26 | 0 |
Ambiguous Genitalia [description not available] | 0 | 3.46 | 8 | 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 | 3.46 | 8 | 0 |
Prosthesis Durability [description not available] | 0 | 5.28 | 20 | 0 |
Foreign-Body Migration Migration of a foreign body from its original location to some other location in the body. | 0 | 4.84 | 12 | 0 |
Bacterial Skin Diseases [description not available] | 0 | 5.71 | 7 | 1 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 5.71 | 7 | 1 |
Nail Abnormalities [description not available] | 0 | 5.03 | 16 | 0 |
Embryopathies [description not available] | 0 | 5.93 | 18 | 0 |
Patency of the Ductus Arteriosus [description not available] | 0 | 3.38 | 2 | 0 |
Hutchinson Gilford Progeria Syndrome [description not available] | 0 | 2.66 | 3 | 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 | 3.38 | 2 | 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 | 2.66 | 3 | 0 |
Polyploid [description not available] | 0 | 2.08 | 1 | 0 |
Muscle Tissue Neoplasms [description not available] | 0 | 2.44 | 2 | 0 |
Alopecia Cicatrisata [description not available] | 0 | 5.03 | 16 | 0 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 5.03 | 16 | 0 |
Congo Virus Infection [description not available] | 0 | 2.08 | 1 | 0 |
Infections, Helicobacter [description not available] | 0 | 4.51 | 5 | 1 |
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 | 4.51 | 5 | 1 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 3.35 | 7 | 0 |
Cutaneous Phaeohyphomycosis [description not available] | 0 | 2.08 | 1 | 0 |
Chromosomal Translocation [description not available] | 0 | 5.56 | 17 | 0 |
Cholangiocellular Carcinoma [description not available] | 0 | 2.51 | 2 | 0 |
Bile Duct Cancer [description not available] | 0 | 2.99 | 4 | 0 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 2.99 | 4 | 0 |
Cholangiocarcinoma A malignant tumor arising from the epithelium of the BILE DUCTS. | 0 | 2.51 | 2 | 0 |
Connective Tissue Disease, Mixed [description not available] | 0 | 2.47 | 2 | 0 |
Mouth Ulcer [description not available] | 0 | 2.08 | 1 | 0 |
Pemphigoid [description not available] | 0 | 2.43 | 2 | 0 |
Pemphigoid, Bullous A chronic and relatively benign subepidermal blistering disease usually of the elderly and without histopathologic acantholysis. | 0 | 2.43 | 2 | 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 | 2.08 | 1 | 0 |
Birt-Hogg-Dubu00E9 Syndrome [description not available] | 0 | 2.08 | 1 | 0 |
Birt-Hogg-Dube Syndrome Autosomal dominant neoplastic syndrome characterised by genodermatosis, lung cysts, spontaneous and recurrent PNEUMOTHORAX; and RENAL CANCER. It is associated with mutations in the folliculin protein gene (FLCN protein). | 0 | 2.08 | 1 | 0 |
Drug Overdose Accidental or deliberate use of a medication or street drug in excess of normal dosage. | 0 | 4.01 | 5 | 0 |
Pancytopenia Deficiency of all three cell elements of the blood, erythrocytes, leukocytes and platelets. | 0 | 2.08 | 1 | 0 |
Deficiency, Vitamin B 12 [description not available] | 0 | 2.51 | 2 | 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 | 2.51 | 2 | 0 |
Autism [description not available] | 0 | 3.38 | 2 | 0 |
Brittle Bone Disease [description not available] | 0 | 4.3 | 4 | 0 |
Arnold-Chiari Deformity [description not available] | 0 | 3.87 | 4 | 0 |
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 | 3.38 | 2 | 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 | 4.3 | 4 | 0 |
Dental Fistula An abnormal passage in the oral cavity on the gingiva. | 0 | 2.68 | 3 | 0 |
Nonodontogenic Cysts Cysts formed from epithelial inclusions in the lines of fusion of the embryonic processes which form the jaws. They include nasopalatine or incisive canal cyst, incisive papilla cyst, globulomaxillary cyst, median palatal cyst, median alveolar cyst, median mandibular cyst, and nasoalveolar cyst. | 0 | 4.67 | 11 | 0 |
Anaplastic Ependymoma [description not available] | 0 | 2.08 | 1 | 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 | 2.08 | 1 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 4.65 | 29 | 0 |
Aural Cholesteatoma [description not available] | 0 | 2.96 | 4 | 0 |
Egyptian Ophthalmia [description not available] | 0 | 2.86 | 4 | 0 |
Trichiasis A disease of the eye in which the eyelashes abnormally turn inwards toward the eyeball producing constant irritation caused by motion of the lids. | 0 | 2.08 | 1 | 0 |
Rhabdomyoma A benign tumor derived from striated muscle. It is extremely rare, generally occurring in the tongue, neck muscles, larynx, uvula, nasal cavity, axilla, vulva, and heart. These tumors are treated by simple excision. (Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1354) | 0 | 2.08 | 1 | 0 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 4.13 | 6 | 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 | 4.13 | 6 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 2.88 | 4 | 0 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 2.38 | 2 | 0 |
Tick Infestations Infestations with soft-bodied (Argasidae) or hard-bodied (Ixodidae) ticks. | 0 | 2.08 | 1 | 0 |
Asystole [description not available] | 0 | 3.35 | 7 | 0 |
Afferent Pupillary Defect [description not available] | 0 | 2.08 | 1 | 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 | 3.35 | 7 | 0 |
Kaposi Disease [description not available] | 0 | 3.08 | 5 | 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 | 3.08 | 5 | 0 |
Cancer of Stomach [description not available] | 0 | 4.08 | 3 | 1 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 1 | 6.08 | 3 | 1 |
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 | 2.43 | 2 | 0 |
Emesis [description not available] | 0 | 6.54 | 11 | 5 |
Gagging Contraction of the muscle of the PHARYNX caused by stimulation of sensory receptors on the SOFT PALATE, by psychic stimuli, or systemically by drugs. | 0 | 4.06 | 3 | 1 |
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 | 7.05 | 7 | 5 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 6.54 | 11 | 5 |
Heroin Abuse [description not available] | 0 | 2.08 | 1 | 0 |
Heroin Dependence Strong dependence or addiction, both physiological and emotional, upon HEROIN. | 0 | 2.08 | 1 | 0 |
Impetigo Contagiosa [description not available] | 0 | 6.35 | 15 | 3 |
Impetigo A common superficial bacterial infection caused by STAPHYLOCOCCUS AUREUS or group A beta-hemolytic streptococci. Characteristics include pustular lesions that rupture and discharge a thin, amber-colored fluid that dries and forms a crust. This condition is commonly located on the face, especially about the mouth and nose. | 0 | 6.35 | 15 | 3 |
Cheilitis Inflammation of the lips. It is of various etiologies and degrees of pathology. | 0 | 2.08 | 1 | 0 |
Colonic Polyps Discrete tissue masses that protrude into the lumen of the COLON. These POLYPS are connected to the wall of the colon either by a stalk, pedunculus, or by a broad base. | 0 | 3.34 | 2 | 0 |
Brown Tendon Sheath Syndrome [description not available] | 0 | 2.94 | 4 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 3.26 | 6 | 0 |
Cholera Infantum [description not available] | 0 | 7.08 | 12 | 3 |
Feuerstein-Mims Syndrome [description not available] | 0 | 2.68 | 3 | 0 |
Encephalomyelitis, Inflammatory [description not available] | 0 | 2.38 | 2 | 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 | 2.48 | 2 | 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 | 2.38 | 2 | 0 |
Mole, Skin [description not available] | 0 | 4.4 | 22 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 2.65 | 3 | 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 | 2.65 | 3 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 4.32 | 4 | 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 | 4.32 | 4 | 0 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 3.08 | 5 | 0 |
Arthritides, Bacterial [description not available] | 0 | 3.36 | 7 | 0 |
Bone Diseases, Infectious Bone diseases caused by pathogenic microorganisms. | 0 | 2.43 | 2 | 0 |
Pus [description not available] | 0 | 6.62 | 20 | 1 |
Heart Disease, Ischemic [description not available] | 0 | 2.1 | 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 | 2.1 | 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 | 3.66 | 10 | 0 |
Acute Brain Injuries [description not available] | 0 | 6.54 | 27 | 2 |
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 | 6.54 | 27 | 2 |
Genetic Diseases, X-Chromosome Linked [description not available] | 0 | 4.46 | 8 | 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 | 2.1 | 1 | 0 |
Giant Cell Tumors Tumors of bone tissue or synovial or other soft tissue characterized by the presence of giant cells. The most common are giant cell tumor of tendon sheath and GIANT CELL TUMOR OF BONE. | 0 | 4.12 | 6 | 0 |
Mandibular Retroposition [description not available] | 0 | 8.74 | 43 | 2 |
Anaphylactic Reaction [description not available] | 0 | 4.67 | 30 | 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 | 4.67 | 30 | 0 |
Fox-Fordyce Disease Chronic pruritic disease, usually in women, characterized by small follicular papular eruptions in APOCRINE GLANDS areas. It is caused by obstruction and rupture of intraepidermal apocrine ducts. | 0 | 1.92 | 1 | 0 |
Enteric Fever [description not available] | 0 | 2.35 | 2 | 0 |
Typhoid Fever An acute systemic febrile infection caused by SALMONELLA TYPHI, a serotype of SALMONELLA ENTERICA. | 0 | 2.35 | 2 | 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 | 6.24 | 148 | 0 |
Muscle Pain [description not available] | 0 | 2.1 | 1 | 0 |
Atrophy, Muscle [description not available] | 0 | 2.67 | 3 | 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 | 2.67 | 3 | 0 |
Myalgia Painful sensation in the muscles. | 0 | 2.1 | 1 | 0 |
Apnea, Central [description not available] | 0 | 3.37 | 2 | 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 | 3.37 | 2 | 0 |
Nanism [description not available] | 0 | 6.16 | 23 | 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 | 6.16 | 23 | 0 |
Hand Dermatosis [description not available] | 0 | 2.72 | 3 | 0 |
Foot Dermatoses Skin diseases of the foot, general or unspecified. | 0 | 2.68 | 3 | 0 |
Hand Dermatoses Skin diseases involving the HANDS. | 0 | 2.72 | 3 | 0 |
Decerebrate Posturing [description not available] | 0 | 2.69 | 3 | 0 |
Chemotherapy-Induced Febrile Neutropenia FEVER accompanied by a significant reduction in NEUTROPHIL count associated with CHEMOTHERAPY. | 0 | 2.1 | 1 | 0 |
Apertognathia [description not available] | 0 | 5.36 | 13 | 1 |
Congestive Ophthalmopathy [description not available] | 0 | 5.04 | 6 | 0 |
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 | 5.04 | 6 | 0 |
Avian Flu [description not available] | 0 | 2.5 | 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 | 2.5 | 2 | 0 |
Bedwetting [description not available] | 0 | 3.72 | 3 | 0 |
Conductive Hearing Loss [description not available] | 0 | 7.06 | 7 | 1 |
Nocturnal Enuresis Involuntary discharge of URINE during sleep at night after expected age of completed development of urinary control. | 0 | 3.72 | 3 | 0 |
Cancer of the Tongue [description not available] | 0 | 3.47 | 8 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 3.47 | 8 | 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 | 9.73 | 45 | 5 |
Auditory Processing Disorder, Central [description not available] | 0 | 3.65 | 3 | 0 |
Craniofacial Microsomia [description not available] | 0 | 4.66 | 6 | 0 |
Cranial Nerve V Injury [description not available] | 0 | 3.47 | 8 | 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 | 4.64 | 6 | 1 |
Hand Deformities Alterations or deviations from normal shape or size which result in a disfigurement of the hand. | 0 | 4.12 | 6 | 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 | 2.1 | 1 | 0 |
Intraventricular Septal Defects [description not available] | 0 | 3.83 | 4 | 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 | 6.89 | 38 | 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 | 3.83 | 4 | 0 |
Albright Hereditary Osteodystrophy without Multiple Hormone Resistance [description not available] | 0 | 2.1 | 1 | 0 |
Chickungunya Fever [description not available] | 0 | 2.52 | 2 | 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 | 7.07 | 83 | 1 |
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 | 7.16 | 15 | 1 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 4.76 | 32 | 0 |
Acute Membranous Gingivitis [description not available] | 0 | 2.44 | 2 | 0 |
Embolus [description not available] | 0 | 3.26 | 6 | 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 | 3.26 | 6 | 0 |
Electrocardiogram QT Prolonged [description not available] | 0 | 2.1 | 1 | 0 |
Long QT Syndrome 1 [description not available] | 0 | 2.1 | 1 | 0 |
Long QT Syndrome A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME. | 0 | 2.1 | 1 | 0 |
Fasciolopsiasis [description not available] | 0 | 2.69 | 3 | 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 | 4.03 | 15 | 0 |
Acute Pain Intensely discomforting, distressful, or agonizing sensation associated with trauma or disease, with well-defined location, character, and timing. | 0 | 3.48 | 1 | 1 |
Ankylosis of Teeth [description not available] | 0 | 2.1 | 1 | 0 |
Click-Murmur Syndrome [description not available] | 0 | 2.67 | 3 | 0 |
Benign Optic Nerve Neoplasm [description not available] | 0 | 2.1 | 1 | 0 |
Cancer of Rectum [description not available] | 0 | 7.25 | 8 | 1 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 7.25 | 8 | 1 |
Ventilator-Associated Pneumonia [description not available] | 0 | 2.1 | 1 | 0 |
Pneumonia, Ventilator-Associated Serious INFLAMMATION of the LUNG in patients who required the use of PULMONARY VENTILATOR. It is usually caused by bacterial CROSS INFECTION in hospitals. | 0 | 2.1 | 1 | 0 |
Odontogenic Cyst, Calcifying A mixed radiolucent-radiopaque lesion of the jaws with features of both a cyst and a solid neoplasm. It is characterized microscopically by an epithelial lining showing a palisaded layer of columnar basal cells, presence of ghost cell keratinization, dentinoid, and calcification. (Stedman, 25th ed) | 0 | 2.1 | 1 | 0 |
Ectopic Ossification [description not available] | 0 | 5.65 | 7 | 1 |
Esophageal Stricture [description not available] | 0 | 3.2 | 6 | 0 |
Esophageal Stenosis A stricture of the ESOPHAGUS. Most are acquired but can be congenital. | 0 | 3.2 | 6 | 0 |
Arrhythmia [description not available] | 0 | 4 | 5 | 0 |
Diastema An abnormal opening or fissure between two adjacent teeth. | 0 | 2.73 | 3 | 0 |
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 | 4.62 | 6 | 0 |
Macrostomia Greatly exaggerated width of the mouth, resulting from failure of union of the maxillary and mandibular processes, with extension of the oral orifice toward the ear. The defect may be unilateral or bilateral. (Dorland, 27th ed) | 0 | 3.25 | 6 | 0 |
Gigantism The condition of accelerated and excessive GROWTH in children or adolescents who are exposed to excess HUMAN GROWTH HORMONE before the closure of EPIPHYSES. It is usually caused by somatotroph hyperplasia or a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. These patients are of abnormally tall stature, more than 3 standard deviations above normal mean height for age. | 0 | 2.11 | 1 | 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. | 1 | 6 | 5 | 0 |
Benign Hypothalamic Neoplasms [description not available] | 0 | 2.52 | 2 | 0 |
Arthropathies [description not available] | 0 | 5.8 | 12 | 2 |
Joint Diseases Diseases involving the JOINTS. | 0 | 5.8 | 12 | 2 |
Tooth Loss The failure to retain teeth as a result of disease or injury. | 0 | 3.87 | 4 | 0 |
Hangman Fracture [description not available] | 0 | 2.1 | 1 | 0 |
Spinal Fractures Broken bones in the vertebral column. | 0 | 2.1 | 1 | 0 |
Cranial Nerve VII Injuries [description not available] | 0 | 4.59 | 10 | 0 |
Langerhans Cell Sarcoma Rare malignant neoplasm of dendritic LANGERHANS CELLS exhibiting atypical cytology, frequent mitoses, and aggressive clinical behavior. They can be distinguished from other histiocytic and dendritic proliferations by immunohistochemical and ultrastructure studies. Cytologically benign proliferations of Langerhans cells are called LANGERHANS CELL HISTIOCYTOSIS. | 0 | 2.13 | 1 | 0 |
Aseptic Necrosis of Bone [description not available] | 0 | 3.86 | 4 | 0 |
Coxa Plana [description not available] | 0 | 2.89 | 4 | 0 |
Osteonecrosis Death of a bone or part of a bone, either atraumatic or posttraumatic. | 0 | 3.86 | 4 | 0 |
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 | 2.66 | 3 | 0 |
Chromosomal Triplication [description not available] | 0 | 7.01 | 30 | 0 |
Autosomal Chromosome Disorders [description not available] | 0 | 4.73 | 31 | 0 |
Bartholin-Patau Syndrome [description not available] | 0 | 2.1 | 1 | 0 |
Atopic Hypersensitivity [description not available] | 0 | 5.9 | 9 | 3 |
Anterior Cerebral Circulation Infarction [description not available] | 0 | 2.52 | 2 | 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 | 2.52 | 2 | 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 | 4.92 | 8 | 0 |
Eye Injuries, Penetrating Deeply perforating or puncturing type intraocular injuries. | 0 | 3.28 | 6 | 0 |
Acanthamoeba Meningoencephalitis [description not available] | 0 | 3.37 | 2 | 0 |
Abscess, Amebic [description not available] | 0 | 4.62 | 6 | 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 | 4.62 | 6 | 0 |
Brain Swelling [description not available] | 0 | 2.66 | 3 | 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 | 2.66 | 3 | 0 |
Coarctation of Aorta [description not available] | 0 | 2.11 | 1 | 0 |
Dextrocardia A congenital defect in which the heart is located on the right side of the THORAX instead of on the left side (levocardia, the normal position). When dextrocardia is accompanied with inverted HEART ATRIA, a right-sided STOMACH, and a left-sided LIVER, the combination is called dextrocardia with SITUS INVERSUS. Dextrocardia may adversely affect other thoracic organs. | 0 | 2.11 | 1 | 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 | 2.11 | 1 | 0 |
Blastomycosis, North American [description not available] | 0 | 4.58 | 10 | 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 | 4.58 | 10 | 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 | 2.11 | 1 | 0 |
Abnormalities, Autosome [description not available] | 0 | 4.8 | 33 | 0 |
Mange, Sarcoptic [description not available] | 0 | 3.48 | 1 | 1 |
Scabies A contagious cutaneous inflammation caused by the bite of the mite SARCOPTES SCABIEI. It is characterized by pruritic papular eruptions and burrows and affects primarily the axillae, elbows, wrists, and genitalia, although it can spread to cover the entire body. | 0 | 3.48 | 1 | 1 |
Acute Cholecystitis [description not available] | 0 | 3.91 | 2 | 1 |
Cholecystitis, Acute Acute inflammation of the GALLBLADDER wall. It is characterized by the presence of ABDOMINAL PAIN; FEVER; and LEUKOCYTOSIS. Gallstone obstruction of the CYSTIC DUCT is present in approximately 90% of the cases. | 0 | 3.91 | 2 | 1 |
Keratocysts [description not available] | 0 | 2.91 | 4 | 0 |
Jaw Cysts Saccular lesions lined with epithelium and contained within pathologically formed cavities in the jaw; also nonepithelial cysts (pseudocysts) as they apply to the jaw, e.g., traumatic or solitary cyst, static bone cavity, and aneurysmal bone cyst. True jaw cysts are classified as odontogenic or nonodontogenic. | 0 | 3.59 | 3 | 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 | 2.11 | 1 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 5.35 | 14 | 1 |
Gastric Diseases [description not available] | 0 | 8 | 6 | 4 |
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 | 3.03 | 1 | 0 |
Abortion, Septic Any type of abortion, induced or spontaneous, that is associated with infection of the UTERUS and its appendages. It is characterized by FEVER, uterine tenderness, and foul discharge. | 0 | 2.11 | 1 | 0 |
Cutaneous Fistula An abnormal passage or communication leading from an internal organ to the surface of the body. | 0 | 4.62 | 6 | 1 |
Buruli Ulcer Disease [description not available] | 0 | 2.11 | 1 | 0 |
Buruli Ulcer A lesion in the skin and subcutaneous tissues due to infections by MYCOBACTERIUM ULCERANS. It was first reported in Uganda, Africa. | 0 | 2.11 | 1 | 0 |
Polyradiculitis [description not available] | 0 | 2.11 | 1 | 0 |
Polyradiculopathy Disease or injury involving multiple SPINAL NERVE ROOTS. Polyradiculitis refers to inflammation of multiple spinal nerve roots. | 0 | 2.11 | 1 | 0 |
Lingual Thyroid A condition characterized by the presence of rudimentary THYROID tissue at the base of the TONGUE. It is due to failed embryonic development and migration of thyroid tissue to its normal location. The lingual thyroid usually cannot maintain adequate hormone production thereby resulting in HYPOTHYROIDISM. | 0 | 2.11 | 1 | 0 |
Nerve Pain [description not available] | 0 | 4.03 | 15 | 0 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 4.03 | 15 | 0 |
Blastocyst Disintegration [description not available] | 0 | 2.11 | 1 | 0 |
Chrysomya bezziana Infection [description not available] | 0 | 2.11 | 1 | 0 |
Amnionitis [description not available] | 0 | 2.49 | 2 | 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 | 2.49 | 2 | 0 |
Connective Tissue Neoplasms [description not available] | 0 | 2.65 | 3 | 0 |
Blood Vessel Tumors [description not available] | 0 | 2.39 | 2 | 0 |
Abnormalities, Mouth [description not available] | 0 | 6.56 | 35 | 0 |
Mandibular Neoplasms Tumors or cancer of the MANDIBLE. | 0 | 3.08 | 5 | 0 |
Injuries, Spinal Cord [description not available] | 0 | 5.19 | 8 | 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 | 5.19 | 8 | 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 | 4.4 | 8 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 4.4 | 8 | 0 |
Elevated ICP (Intracranial Pressure) [description not available] | 0 | 2.11 | 1 | 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 | 2.11 | 1 | 0 |
Tuberculosis, Bovine An infection of cattle caused by MYCOBACTERIUM BOVIS. It is transmissible to man and other animals. | 0 | 2.44 | 2 | 0 |
Hilar Cholangiocarcinoma [description not available] | 0 | 2.11 | 1 | 0 |
Klatskin Tumor Cholangiocarcinoma arising near or at the confluence of the right and left hepatic ducts (COMMON HEPATIC DUCT). These tumors are generally small, sharply localized, and seldom metastasizing. | 0 | 2.11 | 1 | 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 | 4.22 | 18 | 0 |
Ectopic ACTH Syndrome [description not available] | 0 | 2.11 | 1 | 0 |
ACTH Syndrome, Ectopic Symptom complex due to ACTH production by non-pituitary neoplasms. | 0 | 2.11 | 1 | 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 | 3.74 | 11 | 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 | 3.83 | 4 | 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 | 3.83 | 4 | 0 |
Autoimmune Diabetes [description not available] | 0 | 4.63 | 6 | 1 |
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 | 4.63 | 6 | 1 |
Allergy, Drug [description not available] | 0 | 4.96 | 9 | 1 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 4.96 | 9 | 1 |
Granular Cell Myoblastoma [description not available] | 0 | 3.63 | 3 | 0 |
Foot and Mouth Disease [description not available] | 0 | 3.67 | 10 | 0 |
Closed Head Injuries [description not available] | 0 | 3.03 | 1 | 0 |
Benign Infratentorial Neoplasms [description not available] | 0 | 3.4 | 2 | 0 |
Pulsatile Tinnitus [description not available] | 0 | 2.78 | 3 | 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 | 2.78 | 3 | 0 |
Francois Dyscephalic Syndrome [description not available] | 0 | 5.58 | 4 | 0 |
Avulsed Tooth [description not available] | 0 | 3.09 | 5 | 0 |
Anoxia-Ischemia, Brain [description not available] | 0 | 2.11 | 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 | 2.11 | 1 | 0 |
Oral Submucous Fibrosis Irreversible FIBROSIS of the submucosal tissue of the MOUTH. | 0 | 2.11 | 1 | 0 |
Anxiety Neuroses [description not available] | 0 | 2.38 | 2 | 0 |
Disruptive, Impulse Control, and Conduct Disorders Disorders whose essential features are the failure to resist an impulse, drive, or temptation to perform an act that is harmful to the individual or to others. Individuals experience an increased sense of tension prior to the act and pleasure, gratification or release of tension at the time of committing the act. | 0 | 4.03 | 5 | 0 |
Anxiety Disorders Persistent and disabling ANXIETY. | 0 | 2.38 | 2 | 0 |
Academic Disorder, Developmental [description not available] | 0 | 2.73 | 3 | 0 |
Abscess, Intracranial, Subdural [description not available] | 0 | 2.11 | 1 | 0 |
Abscess, Epidural [description not available] | 0 | 2.11 | 1 | 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 | 3.58 | 9 | 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 | 2.73 | 3 | 0 |
Parodontosis [description not available] | 0 | 4.3 | 7 | 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 | 4.3 | 7 | 0 |
Deep Vein Thrombosis [description not available] | 0 | 3.26 | 6 | 0 |
Embolism, Pulmonary [description not available] | 0 | 2.11 | 1 | 0 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 2.11 | 1 | 0 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 3.26 | 6 | 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 | 7.9 | 16 | 2 |
Chondrodysplasia with Hemangioma [description not available] | 0 | 3.3 | 2 | 0 |
Chloracne ACNE-like skin eruptions caused by exposure to CHLORINE-containing compounds. Exposure can be by inhalation, ingestion, or through the skin. Chloracne is often seen in people who have occupational contact with chlorinated pesticides, wood preservatives, and sealants. | 0 | 2.11 | 1 | 0 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 3.58 | 9 | 0 |
Basilar Skull Fracture [description not available] | 0 | 3.03 | 1 | 0 |
Cranial Nerve II Diseases [description not available] | 0 | 5.15 | 11 | 0 |
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 | 5.15 | 11 | 0 |
Acid Aspiration Syndrome [description not available] | 0 | 4.46 | 5 | 1 |
Pneumonia, Aspiration A type of lung inflammation resulting from the aspiration of food, liquid, or gastric contents into the upper RESPIRATORY TRACT. | 0 | 4.46 | 5 | 1 |
Birnaviridae Infections Virus diseases caused by the BIRNAVIRIDAE. | 0 | 2.13 | 1 | 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 | 5.19 | 11 | 0 |
Brain Contusion A bruise of the brain from an impact of the skull. | 0 | 3.04 | 1 | 0 |
Cranial Nerve I Injury [description not available] | 0 | 3.04 | 1 | 0 |
Microstomia A congenital defect in which the mouth is unusually small. (Dorland, 27th ed) | 0 | 3.27 | 6 | 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 | 4.38 | 8 | 0 |
Hendra Virus Infections [description not available] | 0 | 2.11 | 1 | 0 |
Ornithosis [description not available] | 0 | 2.66 | 3 | 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 | 3.9 | 13 | 0 |
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 | 2.66 | 3 | 0 |
Deficiency, Vitamin A [description not available] | 0 | 2.65 | 3 | 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 | 2.65 | 3 | 0 |
Cancrum Oris [description not available] | 0 | 3.39 | 7 | 0 |
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 | 4.14 | 3 | 0 |
Siamese Twins [description not available] | 0 | 4.17 | 3 | 0 |
Mediastinal Diseases Disorders of the mediastinum, general or unspecified. | 0 | 2.83 | 3 | 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 | 4.59 | 6 | 0 |
Airway Hyper-Responsiveness [description not available] | 0 | 11.77 | 58 | 2 |
Odontalgia [description not available] | 0 | 2.7 | 3 | 0 |
Toothache Pain in the adjacent areas of the teeth. | 0 | 2.7 | 3 | 0 |
Cancer of Liver [description not available] | 0 | 3.36 | 7 | 0 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 3.36 | 7 | 0 |
Abdominal Epilepsy [description not available] | 0 | 2.46 | 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 | 2.46 | 2 | 0 |
Actinomycetales Infections Infections with bacteria of the order ACTINOMYCETALES. | 0 | 2.8 | 3 | 0 |
Leukoma [description not available] | 0 | 2.67 | 3 | 0 |
Brain Diseases, Metabolic, Familial [description not available] | 0 | 2.13 | 1 | 0 |
Corneal Opacity Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque. | 0 | 2.67 | 3 | 0 |
Abnormality, Torsion [description not available] | 0 | 2.36 | 2 | 0 |
Infections, Nematode [description not available] | 0 | 5.89 | 9 | 1 |
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 | 4.4 | 8 | 0 |
Blood Diseases [description not available] | 0 | 3.07 | 5 | 0 |
Hematologic Diseases Disorders of the blood and blood forming tissues. | 0 | 3.07 | 5 | 0 |
Amyloidosis, Hereditary [description not available] | 0 | 2.13 | 1 | 0 |
Genetic Skin Diseases [description not available] | 0 | 3.41 | 2 | 0 |
Amyloidosis, Familial Diseases in which there is a familial pattern of AMYLOIDOSIS. | 0 | 2.13 | 1 | 0 |
Postherpetic Neuralgia [description not available] | 0 | 2.11 | 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 | 2.11 | 1 | 0 |
Precordial Catch [description not available] | 0 | 3.87 | 4 | 0 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 3.87 | 4 | 0 |
Angiomyxoma [description not available] | 0 | 3.56 | 3 | 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 | 4.56 | 10 | 0 |
Arterial Diseases, Carotid [description not available] | 0 | 2.67 | 3 | 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 | 2.67 | 3 | 0 |
Frostbite Damage to tissues as the result of low environmental temperatures. | 0 | 2.47 | 2 | 0 |
Foot Injuries General or unspecified injuries involving the foot. | 0 | 3.83 | 4 | 0 |
Hand Injuries General or unspecified injuries to the hand. | 0 | 3.47 | 8 | 0 |
Infectious Bovine Rhinotracheitis A herpesvirus infection of CATTLE characterized by INFLAMMATION and NECROSIS of the mucous membranes of the upper RESPIRATORY TRACT. | 0 | 6.39 | 23 | 2 |
Orthopedic Disorders [description not available] | 0 | 2.64 | 3 | 0 |
Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | 0 | 2.64 | 3 | 0 |
Bronchospasm, Exercise-Induced [description not available] | 0 | 7.18 | 8 | 1 |
Asthma, Exercise-Induced Asthma attacks following a period of exercise. Usually the induced attack is short-lived and regresses spontaneously. The magnitude of postexertional airway obstruction is strongly influenced by the environment in which exercise is performed (i.e. inhalation of cold air during physical exertion markedly augments the severity of the airway obstruction; conversely, warm humid air blunts or abolishes it). | 0 | 7.18 | 8 | 1 |
Smoking Cessation Discontinuing the habit of SMOKING. | 0 | 5.27 | 4 | 3 |
Drug Withdrawal Symptoms [description not available] | 0 | 3.93 | 2 | 1 |
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 | 3.93 | 2 | 1 |
Autosomal Dominant Cerebellar Ataxia, Type II [description not available] | 0 | 2.13 | 1 | 0 |
Dysarthosis [description not available] | 0 | 2.42 | 2 | 0 |
Clasp-Knife Spasticity [description not available] | 0 | 4.13 | 3 | 1 |
Autosomal Dominant Hereditary Spastic Paraplegia [description not available] | 0 | 2.13 | 1 | 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 | 4.13 | 3 | 1 |
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 | 2.13 | 1 | 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 | 2.13 | 1 | 0 |
Carcinoma, Mucoepidermoid A tumor of both low- and high-grade malignancy. The low-grade grow slowly, appear in any age group, and are readily cured by excision. The high-grade behave aggressively, widely infiltrate the salivary gland and produce lymph node and distant metastases. Mucoepidermoid carcinomas account for about 21% of the malignant tumors of the parotid gland and 10% of the sublingual gland. They are the most common malignant tumor of the parotid. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p575; Holland et al., Cancer Medicine, 3d ed, p1240) | 0 | 2.43 | 2 | 0 |
Genital Herpes [description not available] | 0 | 2.43 | 2 | 0 |
Herpes Genitalis Infection of the genitals (GENITALIA) with HERPES SIMPLEX VIRUS in either the males or the females. | 0 | 2.43 | 2 | 0 |
Ewing Sarcoma [description not available] | 0 | 2.42 | 2 | 0 |
Sarcoma, Ewing A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. The tumor occurs usually before the age of 20, about twice as frequently in males as in females. | 0 | 2.42 | 2 | 0 |
Alveolitis, Fibrosing [description not available] | 0 | 3.06 | 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 | 3.06 | 5 | 0 |
Great Pox [description not available] | 0 | 5.49 | 27 | 0 |
Microglossia [description not available] | 0 | 2.67 | 3 | 0 |
Syphilis A contagious venereal disease caused by the spirochete TREPONEMA PALLIDUM. | 0 | 5.49 | 27 | 0 |
Osteoid Osteoma [description not available] | 0 | 2.39 | 2 | 0 |
Scrofuloderma [description not available] | 0 | 3.55 | 9 | 0 |
Pulmonary Consumption [description not available] | 0 | 5.86 | 9 | 1 |
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 | 2.9 | 4 | 0 |
Bone Tuberculosis [description not available] | 0 | 2.13 | 1 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 5.86 | 9 | 1 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 2.13 | 1 | 0 |
Minimal Disease, Residual [description not available] | 0 | 3.92 | 4 | 0 |
Primate Diseases Diseases of animals within the order PRIMATES. This term includes diseases of Haplorhini and Strepsirhini. | 0 | 2.7 | 3 | 0 |
Pneumonia, Lipid Pneumonia due to aspiration or inhalation of various oily or fatty substances. | 0 | 2.36 | 2 | 0 |
Break-Bone Fever [description not available] | 0 | 2.13 | 1 | 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 | 2.13 | 1 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 2.92 | 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 | 2.92 | 4 | 0 |
Plasma Cell Tumor [description not available] | 0 | 4.19 | 18 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 4.19 | 18 | 0 |
Jaw Fractures Fractures of the upper or lower jaw. | 0 | 5.47 | 16 | 0 |
Esophageal Perforation An opening or hole in the ESOPHAGUS that is caused by TRAUMA, injury, or pathological process. | 0 | 2.72 | 3 | 0 |
Hyperprolactinaemia [description not available] | 0 | 2.51 | 2 | 0 |
Galactorrhea Excessive or inappropriate LACTATION in females or males, and not necessarily related to PREGNANCY. Galactorrhea can occur either unilaterally or bilaterally, and be profuse or sparse. Its most common cause is HYPERPROLACTINEMIA. | 0 | 2.15 | 1 | 0 |
Hyperprolactinemia Increased levels of PROLACTIN in the BLOOD, which may be associated with AMENORRHEA and GALACTORRHEA. Relatively common etiologies include PROLACTINOMA, medication effect, KIDNEY FAILURE, granulomatous diseases of the PITUITARY GLAND, and disorders which interfere with the hypothalamic inhibition of prolactin release. Ectopic (non-pituitary) production of prolactin may also occur. (From Joynt, Clinical Neurology, 1992, Ch36, pp77-8) | 0 | 2.51 | 2 | 0 |
Bronchial Diseases Diseases involving the BRONCHI. | 0 | 5.26 | 9 | 0 |
Absence of Brain, Congenital [description not available] | 0 | 3.84 | 4 | 0 |
Diaphragmatic Hernia [description not available] | 0 | 4.15 | 6 | 0 |
Cerebral Ischemia [description not available] | 0 | 2.72 | 3 | 0 |
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 | 2.72 | 3 | 0 |
Dental Diseases [description not available] | 0 | 4.12 | 3 | 0 |
Blue-Eared Pig Disease [description not available] | 0 | 4.54 | 5 | 1 |
Acute Lymphoid Leukemia [description not available] | 0 | 2.94 | 4 | 0 |
Opportunistic Infections An infection caused by an organism which becomes pathogenic under certain conditions, e.g., during immunosuppression. | 0 | 3.52 | 8 | 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 | 2.94 | 4 | 0 |
Bile Duct Obstruction [description not available] | 0 | 4.03 | 5 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 4.03 | 5 | 0 |
Action Tremor [description not available] | 0 | 2.49 | 2 | 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 | 2.49 | 2 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 2.13 | 1 | 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 | 2.13 | 1 | 0 |
Ritter Disease [description not available] | 0 | 2.94 | 4 | 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 | 3.08 | 5 | 0 |
Acidosis, Respiratory Respiratory retention of carbon dioxide. It may be chronic or acute. | 0 | 2.44 | 2 | 0 |
Callous-Unemotional Traits [description not available] | 0 | 2.15 | 1 | 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 | 2.15 | 1 | 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 | 2.15 | 1 | 0 |
Amnesia-Memory Loss [description not available] | 0 | 2.15 | 1 | 0 |
Hallucination of Body Sensation [description not available] | 0 | 2.37 | 2 | 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 | 2.15 | 1 | 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 | 2.37 | 2 | 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 | 2.15 | 1 | 0 |
Dwarfism, Growth Hormone Deficiency [description not available] | 0 | 2.15 | 1 | 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 | 2.15 | 1 | 0 |
Palatal Neoplasms Tumors or cancer of the PALATE, including those of the hard palate, soft palate and UVULA. | 0 | 3.58 | 9 | 0 |
Alcohol Abuse [description not available] | 0 | 4.84 | 4 | 2 |
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 | 4.84 | 4 | 2 |
Bronchial Pneumonia [description not available] | 0 | 3.23 | 6 | 0 |
Leishmania Infection [description not available] | 0 | 4.3 | 20 | 0 |
Lupus Erythematosus, Chronic Cutaneous [description not available] | 0 | 2.67 | 3 | 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 | 4.3 | 20 | 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 | 2.67 | 3 | 0 |
Experimental Pneumococcal Meningitis [description not available] | 0 | 5.66 | 7 | 1 |
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 | 5.66 | 7 | 1 |
Autosomal Hemophilia A [description not available] | 0 | 2.87 | 4 | 0 |
Hemophilia A The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage. | 0 | 2.87 | 4 | 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 | 3.12 | 5 | 0 |
Lip Diseases Diseases involving the LIP. | 0 | 5.39 | 14 | 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 | 2.69 | 3 | 0 |
Intestinal Volvulus A twisting in the intestine (INTESTINES) that can cause INTESTINAL OBSTRUCTION. | 0 | 2.04 | 1 | 0 |
Acariasis [description not available] | 0 | 4.31 | 20 | 0 |
Boils [description not available] | 0 | 8.82 | 26 | 1 |
Cavernous Sinus Thrombophlebitis [description not available] | 0 | 3.06 | 5 | 0 |
Infections, Poxviridae [description not available] | 0 | 2.88 | 4 | 0 |
Cancer, Second Primary [description not available] | 0 | 2.04 | 1 | 0 |
Cholangitis Inflammation of the biliary ductal system (BILE DUCTS); intrahepatic, extrahepatic, or both. | 0 | 2.91 | 4 | 0 |
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 | 7.83 | 17 | 2 |
Bone Diseases, Developmental Diseases resulting in abnormal GROWTH or abnormal MORPHOGENESIS of BONES. | 0 | 6.23 | 25 | 0 |
Brain Vascular Disorders [description not available] | 0 | 2.65 | 3 | 0 |
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 | 2.65 | 3 | 0 |
Bone Diseases Diseases of BONES. | 0 | 3.93 | 13 | 0 |
Condition, Preneoplastic [description not available] | 0 | 3.58 | 9 | 0 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 3.58 | 9 | 0 |
Birth Injuries Mechanical or anoxic trauma incurred by the infant during labor or delivery. | 0 | 6.54 | 27 | 0 |
Diseases of Immune System [description not available] | 0 | 4.92 | 39 | 0 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 4.92 | 39 | 0 |
Diseases of Endocrine System [description not available] | 0 | 2.85 | 4 | 0 |
Endocrine System Diseases Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES. | 0 | 2.85 | 4 | 0 |
Starvation Lengthy and continuous deprivation of food. (Stedman, 25th ed) | 0 | 1.92 | 1 | 0 |
Ametropia [description not available] | 0 | 2.34 | 2 | 0 |
Refractive Errors Deviations from the average or standard indices of refraction of the eye through its dioptric or refractive apparatus. | 0 | 2.34 | 2 | 0 |
Infarct [description not available] | 0 | 1.92 | 1 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 4.18 | 18 | 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 | 4.18 | 18 | 0 |
Liver Dysfunction [description not available] | 0 | 2.63 | 3 | 0 |
Liver Diseases Pathological processes of the LIVER. | 0 | 2.63 | 3 | 0 |
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 | 3.55 | 9 | 0 |
Neoplasms, Nervous System [description not available] | 0 | 1.92 | 1 | 0 |
Cranial Sinus Thrombosis [description not available] | 0 | 3.03 | 5 | 0 |
As If Personality [description not available] | 0 | 3.04 | 5 | 0 |
Erysipelothrix Infections Infections with bacteria of the genus ERYSIPELOTHRIX. | 0 | 2.38 | 2 | 0 |
Cartilage Fractures [description not available] | 0 | 5.64 | 19 | 0 |
Inguinal Hernia [description not available] | 0 | 2.38 | 2 | 0 |
Hernia, Inguinal An abdominal hernia with an external bulge in the GROIN region. It can be classified by the location of herniation. Indirect inguinal hernias occur through the internal inguinal ring. Direct inguinal hernias occur through defects in the ABDOMINAL WALL (transversalis fascia) in Hesselbach's triangle. The former type is commonly seen in children and young adults; the latter in adults. | 0 | 2.38 | 2 | 0 |
Immune Reconstitution Disease [description not available] | 0 | 2.47 | 2 | 0 |
Wasting Disease [description not available] | 0 | 2.05 | 1 | 0 |
Indigestion [description not available] | 0 | 4.11 | 3 | 1 |
Dyspepsia Impaired digestion, especially after eating. | 0 | 4.11 | 3 | 1 |
Common Variable Hypogammaglobulinemia [description not available] | 0 | 2.42 | 2 | 0 |
Common Variable Immunodeficiency Heterogeneous group of immunodeficiency syndromes characterized by hypogammaglobulinemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections. | 0 | 2.42 | 2 | 0 |
Flaccid Quadriplegia [description not available] | 0 | 3.24 | 6 | 0 |
Skin Diseases, Vascular Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area. | 0 | 2.93 | 4 | 0 |
Acoustic Neuroma [description not available] | 0 | 2.94 | 4 | 0 |
Hypermobility, Joint [description not available] | 0 | 2.94 | 4 | 0 |
Anhidrosis [description not available] | 0 | 2.44 | 2 | 0 |
Esophageal Fistula Abnormal passage communicating with the ESOPHAGUS. The most common type is TRACHEOESOPHAGEAL FISTULA between the esophagus and the TRACHEA. | 0 | 2.66 | 3 | 0 |
Blood Pressure, Low [description not available] | 0 | 4.25 | 4 | 1 |
Tachyarrhythmia [description not available] | 0 | 4.62 | 6 | 1 |
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. | 1 | 6.25 | 4 | 1 |
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 | 4.62 | 6 | 1 |
Injuries, Radiation [description not available] | 0 | 6.93 | 17 | 1 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 2.05 | 1 | 0 |
Idiopathic Pulmonary Fibrosis A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change. | 0 | 2.05 | 1 | 0 |
Congenital Myotonic Dystrophy [description not available] | 0 | 2.72 | 3 | 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 | 2.72 | 3 | 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 | 2.42 | 2 | 0 |
Monosomy The condition in which one chromosome of a pair is missing. In a normally diploid cell it is represented symbolically as 2N-1. | 0 | 2.05 | 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 | 5.96 | 5 | 2 |
Abnormal Deep Tendon Reflex [description not available] | 0 | 5.52 | 6 | 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 | 5.52 | 6 | 1 |
Acidosis, Diabetic [description not available] | 0 | 2.46 | 2 | 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 | 2.46 | 2 | 0 |
Histoplasma capsulatum Infection [description not available] | 0 | 5.18 | 4 | 1 |
Cerebral Cryptococcosis [description not available] | 0 | 2.05 | 1 | 0 |
Ecthyma An ulcerative pyoderma usually caused by group A beta-hemolytic streptococcal infection at the site of minor trauma. (Dorland, 27th ed) | 0 | 2.4 | 2 | 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 | 4.45 | 8 | 0 |
Agricultural Worker Disease [description not available] | 0 | 2.41 | 2 | 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 | 5.18 | 4 | 1 |
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 | 2.05 | 1 | 0 |
Burkholderia pseudomallei Infection [description not available] | 0 | 2.05 | 1 | 0 |
Esophageal Diseases Pathological processes in the ESOPHAGUS. | 0 | 5.67 | 7 | 1 |
Drooling [description not available] | 0 | 2.05 | 1 | 0 |
Sialorrhea Increased salivary flow. | 0 | 2.05 | 1 | 0 |
XYY Karyotype Abnormal genetic constitution in males characterized by an extra Y chromosome. | 0 | 2.05 | 1 | 0 |
Acrocallosal Syndrome Autosomal recessive syndrome characterized by hypogenesis or agenesis of CORPUS CALLOSUM. Clinical features include MENTAL RETARDATION; CRANIOFACIAL ABNORMALITIES; digital malformations, and growth retardation. | 0 | 2.45 | 2 | 0 |
Fibrocartilaginous Dysplasia of Bone [description not available] | 0 | 3.65 | 10 | 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 | 3.65 | 10 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Craniofacial Pain Syndromes [description not available] | 0 | 3.47 | 8 | 0 |
Asialia [description not available] | 0 | 2.46 | 2 | 0 |
Hoarseness An unnaturally deep or rough quality of voice. | 0 | 4.97 | 9 | 1 |
Xerostomia Decreased salivary flow. | 0 | 2.46 | 2 | 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 | 4.06 | 3 | 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 | 3.35 | 7 | 0 |
Infectious Keratoconjunctivitis [description not available] | 0 | 2.05 | 1 | 0 |
Shingles [description not available] | 0 | 4.28 | 7 | 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 | 4.28 | 7 | 0 |
Ankylosis Fixation and immobility of a joint. | 0 | 3.56 | 9 | 0 |
Extravascular Hemolysis [description not available] | 0 | 3.46 | 8 | 0 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 3.46 | 8 | 0 |
Dental Enamel Hypoplasia An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors. | 0 | 3.67 | 10 | 0 |
Anankastic Personality [description not available] | 0 | 2.67 | 3 | 0 |
Consciousness, Loss of [description not available] | 0 | 2.89 | 4 | 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 | 2.67 | 3 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 4.19 | 18 | 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 | 4.19 | 18 | 0 |
Bovine Hemorrhagic Syndrome [description not available] | 0 | 2.05 | 1 | 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 | 2.47 | 2 | 0 |
Leukocytopenia [description not available] | 0 | 2.43 | 2 | 0 |
Thrombopenia [description not available] | 0 | 2.4 | 2 | 0 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 2.43 | 2 | 0 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 2.4 | 2 | 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 | 2.46 | 2 | 0 |
Black Death [description not available] | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Chloroma [description not available] | 0 | 2.46 | 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 | 2.46 | 2 | 0 |
Fetal Growth Restriction [description not available] | 0 | 4.77 | 12 | 0 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 4.77 | 12 | 0 |
Lymphoma of Mucosa-Associated Lymphoid Tissue [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Tracheal Neoplasms New abnormal growth of tissue in the TRACHEA. | 0 | 2.67 | 3 | 0 |
Brachial Paresis [description not available] | 0 | 2.44 | 2 | 0 |
Acquired Facial Neuropathy [description not available] | 0 | 2.92 | 4 | 0 |
Ear Deformities, Acquired Distortion or disfigurement of the ear caused by disease or injury after birth. | 0 | 5.53 | 17 | 0 |
Sebaceous Gland Diseases Diseases of the sebaceous glands such as sebaceous hyperplasia and sebaceous cell carcinoma (SEBACEOUS GLAND NEOPLASMS). | 0 | 2.05 | 1 | 0 |
Lower Extremity Weakness, Spastic [description not available] | 0 | 2.05 | 1 | 0 |
Cystic Echinococcosis [description not available] | 0 | 2.43 | 2 | 0 |
Allodynia [description not available] | 0 | 2.43 | 2 | 0 |
Left Ventricular Dysfunction [description not available] | 0 | 2.05 | 1 | 0 |
Apical Ballooning Syndrome [description not available] | 0 | 2.46 | 2 | 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 | 2.05 | 1 | 0 |
Takotsubo Cardiomyopathy A transient left ventricular apical dysfunction or ballooning accompanied by electrocardiographic (ECG) T wave inversions. This abnormality is associated with high levels of CATECHOLAMINES, either administered or endogenously secreted from a tumor or during extreme stress. | 0 | 2.46 | 2 | 0 |
Fractures, Closed Fractures in which the break in bone is not accompanied by an external wound. | 0 | 5.67 | 7 | 1 |
Congenital Oculofacial Paralysis, Moebius [description not available] | 0 | 2.44 | 2 | 0 |
Amentia [description not available] | 0 | 2.39 | 2 | 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 | 2.39 | 2 | 0 |
Chronic Wasting Disease [description not available] | 0 | 2.05 | 1 | 0 |
Anotia [description not available] | 0 | 2.05 | 1 | 0 |
Arthritis, Degenerative [description not available] | 0 | 2.9 | 4 | 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 | 2.9 | 4 | 0 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 4.3 | 4 | 1 |
Neuroma A tumor made up of nerve cells and nerve fibers. (Dorland, 27th ed) | 0 | 2.34 | 2 | 0 |
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 | 2.86 | 4 | 0 |
Acute Rheumatic Fever [description not available] | 0 | 3.32 | 7 | 0 |
Gas Poisoning Poisoning that results from exposure to gases such as CARBON MONOXIDE; NOBLE GASES; OXYGEN; or NATURAL GAS. | 0 | 1.92 | 1 | 0 |
Eye Hemorrhage Intraocular hemorrhage from the vessels of various tissues of the eye. | 0 | 2.33 | 2 | 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 | 2.87 | 4 | 0 |
Hematemesis Vomiting of blood that is either fresh bright red, or older coffee-ground in character. It generally indicates bleeding of the UPPER GASTROINTESTINAL TRACT. | 0 | 3.12 | 5 | 0 |
Hemorrhagic Diathesis [description not available] | 0 | 3.2 | 6 | 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 | 3.2 | 6 | 0 |
Central Nervous System Cysticercosis [description not available] | 0 | 1.92 | 1 | 0 |
Coenuri Infection [description not available] | 0 | 1.92 | 1 | 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 | 1.92 | 1 | 0 |
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 | 1.92 | 1 | 0 |
Amyloid Deposits [description not available] | 0 | 2.05 | 1 | 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 | 2.45 | 2 | 0 |
Alkalosis A pathological condition that removes acid or adds base to the body fluids. | 0 | 2.41 | 2 | 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 | 2.05 | 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 | 2.45 | 2 | 0 |
Injuries, Spinal [description not available] | 0 | 5.51 | 6 | 1 |
Aphthae [description not available] | 0 | 3.76 | 2 | 1 |
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 | 3.76 | 2 | 1 |
Food Poisoning, Staphylococcal [description not available] | 0 | 3.36 | 7 | 0 |
Adrenal Cancer [description not available] | 0 | 2.97 | 1 | 0 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 2.97 | 1 | 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 | 2.97 | 1 | 0 |
Aortic Incompetence [description not available] | 0 | 2.66 | 3 | 0 |
Episcleritis [description not available] | 0 | 2.46 | 2 | 0 |
Aortitis Inflammation of the wall of the AORTA. | 0 | 2.05 | 1 | 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 | 2.66 | 3 | 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 | 2.46 | 2 | 0 |
Infections, Pneumovirus [description not available] | 0 | 2.05 | 1 | 0 |
Factitious Disorders Disorders characterized by physical or psychological symptoms that are not real, genuine, or natural. | 0 | 2.05 | 1 | 0 |
Nearsightedness [description not available] | 0 | 3.35 | 7 | 0 |
Retinal Pigment Epithelial Detachment [description not available] | 0 | 2.39 | 2 | 0 |
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 | 3.35 | 7 | 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 | 2.39 | 2 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 2.05 | 1 | 0 |
Dementia Praecox [description not available] | 0 | 3.39 | 7 | 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 | 2.05 | 1 | 0 |
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 | 3.39 | 7 | 0 |
Discitis Inflammation of an INTERVERTEBRAL DISC or disk space which may lead to disk erosion. Until recently, discitis has been defined as a nonbacterial inflammation and has been attributed to aseptic processes (e.g., chemical reaction to an injected substance). However, recent studies provide evidence that infection may be the initial cause, but perhaps not the promoter, of most cases of discitis. Discitis has been diagnosed in patients following discography, myelography, lumbar puncture, paravertebral injection, and obstetrical epidural anesthesia. Discitis following chemonucleolysis (especially with chymopapain) is attributed to chemical reaction by some and to introduction of microorganisms by others. | 0 | 2.05 | 1 | 0 |
Bacterial Endocarditides [description not available] | 0 | 4.4 | 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 | 4.4 | 8 | 0 |
Blepharitis Inflammation of the eyelids. | 0 | 3.07 | 5 | 0 |
Coagulation Disorders, Blood [description not available] | 0 | 3.2 | 6 | 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 | 3.2 | 6 | 0 |
Lentigines [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Carcinoma, Colloid [description not available] | 0 | 2.38 | 2 | 0 |
Cancer of Duodenum [description not available] | 0 | 2.05 | 1 | 0 |
Adenocarcinoma, Mucinous An adenocarcinoma producing mucin in significant amounts. (From Dorland, 27th ed) | 0 | 2.38 | 2 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 2.06 | 1 | 0 |
Bannayan-Riley-Ruvalcaba Syndrome [description not available] | 0 | 2.06 | 1 | 0 |
Hamartoma Syndrome, Multiple A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE. | 0 | 2.06 | 1 | 0 |
Benedict Syndrome [description not available] | 0 | 2.95 | 4 | 0 |
Infections, Proteus [description not available] | 0 | 3.77 | 2 | 1 |
Angiomatosis Oculoorbital-Thalamic Syndrome [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Acanthoma A neoplasm composed of squamous or epidermal cells. | 0 | 2.44 | 2 | 0 |
Melanoma, Amelanotic An unpigmented malignant melanoma. It is an anaplastic melanoma consisting of cells derived from melanoblasts but not forming melanin. (Dorland, 27th ed; Stedman, 25th ed) | 0 | 2.72 | 3 | 0 |
Kawasaki Disease [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 4.15 | 6 | 0 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 2.38 | 2 | 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 | 4.15 | 6 | 0 |
Sinoatrial Block Disturbance in the atrial activation that is caused by transient failure of impulse conduction from the SINOATRIAL NODE to the HEART ATRIA. It is characterized by a delayed in heartbeat and pauses between P waves in an ELECTROCARDIOGRAM. | 0 | 2.42 | 2 | 0 |
Glandular Fever [description not available] | 0 | 2.62 | 3 | 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 | 2.62 | 3 | 0 |
Cancer of Pelvis [description not available] | 0 | 2.34 | 2 | 0 |
Skin Syphilis [description not available] | 0 | 3.04 | 5 | 0 |
Bone Inflammation [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 | 3.03 | 5 | 0 |
Neuroses [description not available] | 0 | 3.19 | 6 | 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 | 3.19 | 6 | 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 | 3.33 | 7 | 0 |
Fusobacterium Infections Infections with bacteria of the genus FUSOBACTERIUM. | 0 | 2.33 | 2 | 0 |
Congenital Dysplasia Of The Hip [description not available] | 0 | 3.34 | 7 | 0 |
Fungal Lung Diseases [description not available] | 0 | 3.21 | 6 | 0 |
Diseases in Twins Disorders affecting TWINS, one or both, at any age. | 0 | 6.11 | 22 | 0 |
Libman-Sacks Disease [description not available] | 0 | 5.87 | 9 | 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 | 5.87 | 9 | 1 |
Neutropenia A decrease in the number of NEUTROPHILS found in the blood. | 0 | 3.09 | 5 | 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 | 2.88 | 4 | 0 |
Alveolar Bone Atrophy [description not available] | 0 | 2.47 | 2 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 4.82 | 13 | 0 |
Pregnancy in Diabetes [description not available] | 0 | 2.89 | 4 | 0 |
Injuries, Tendon [description not available] | 0 | 3.78 | 4 | 0 |
Aortic Dissection [description not available] | 0 | 2.05 | 1 | 0 |
Acute Post-Traumatic Stress Disorder [description not available] | 0 | 2.38 | 2 | 0 |
Stress Disorders, Post-Traumatic A class of traumatic stress disorders with symptoms that last more than one month. | 0 | 2.38 | 2 | 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 | 2.69 | 3 | 0 |
Root Resorption Resorption in which cementum or dentin is lost from the root of a tooth owing to cementoclastic or osteoclastic activity in conditions such as trauma of occlusion or neoplasms. (Dorland, 27th ed) | 0 | 2.06 | 1 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 2.88 | 4 | 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 | 2.88 | 4 | 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 | 2.87 | 4 | 0 |
Ear Infection [description not available] | 0 | 4.67 | 11 | 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 | 6.89 | 27 | 3 |
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 | 5.53 | 17 | 1 |
Central Diabetes Insipidus [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Thalassemias [description not available] | 0 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Kaposi Sarcoma [description not available] | 0 | 2.06 | 1 | 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 | 2.06 | 1 | 0 |
Persistent Truncus Arteriosus [description not available] | 0 | 2.07 | 1 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 2.06 | 1 | 0 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 2.06 | 1 | 0 |
Pancreatic Pseudocyst Cyst-like space not lined by EPITHELIUM and contained within the PANCREAS. Pancreatic pseudocysts account for most of the cystic collections in the pancreas and are often associated with chronic PANCREATITIS. | 0 | 2.06 | 1 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 2.65 | 3 | 0 |
Hepatocellular Carcinoma [description not available] | 0 | 2.41 | 2 | 0 |
Cancer of Kidney [description not available] | 0 | 3.63 | 3 | 0 |
Experimental Neoplasms [description not available] | 0 | 3.46 | 8 | 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 | 2.41 | 2 | 0 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 3.63 | 3 | 0 |
Hepatoblastoma A malignant neoplasm occurring in young children, primarily in the liver, composed of tissue resembling embryonal or fetal hepatic epithelium, or mixed epithelial and mesenchymal tissues. (Stedman, 25th ed) | 0 | 2.05 | 1 | 0 |
Nervous System Disorders [description not available] | 0 | 5.17 | 7 | 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 | 5.17 | 7 | 0 |
Desmoid [description not available] | 0 | 2.06 | 1 | 0 |
Fibromatosis, Aggressive A childhood counterpart of abdominal or extra-abdominal desmoid tumors, characterized by firm subcutaneous nodules that grow rapidly in any part of the body but do not metastasize. The adult form of abdominal fibromatosis is FIBROMATOSIS, ABDOMINAL. (Stedman, 25th ed) | 0 | 2.06 | 1 | 0 |
Emphysema A pathological accumulation of air in tissues or organs. | 0 | 3.35 | 7 | 0 |
Cardiac Failure [description not available] | 0 | 6.6 | 7 | 3 |
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 | 6.6 | 7 | 3 |
Anorectal Anomalies [description not available] | 0 | 2.06 | 1 | 0 |
Exomphalos [description not available] | 0 | 3.21 | 6 | 0 |
Hernia, Umbilical A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of OMENTUM or SMALL INTESTINE. The vast majority of umbilical hernias are congenital but can be acquired due to severe abdominal distention. | 0 | 3.21 | 6 | 0 |
Besnoitiasis [description not available] | 0 | 2.91 | 4 | 0 |
Xeroderma [description not available] | 0 | 3.36 | 2 | 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 | 3.36 | 2 | 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 | 2.06 | 1 | 0 |
Biliary Calculi [description not available] | 0 | 2.89 | 4 | 0 |
Anorectal Diseases [description not available] | 0 | 2.48 | 2 | 0 |
Sigmoid Colon Diseases [description not available] | 0 | 2.06 | 1 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 2.48 | 2 | 0 |
Gallstones Solid crystalline precipitates in the BILIARY TRACT, usually formed in the GALLBLADDER, resulting in the condition of CHOLELITHIASIS. Gallstones, derived from the BILE, consist mainly of calcium, cholesterol, or bilirubin. | 0 | 2.89 | 4 | 0 |
Cancer of Jaw [description not available] | 0 | 3.82 | 4 | 0 |
Fifth Phacomatosis [description not available] | 0 | 3.34 | 2 | 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 | 3.34 | 2 | 0 |
Exsanguinating Hemorrhage [description not available] | 0 | 2.07 | 1 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 2.06 | 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 | 2.06 | 1 | 0 |
Idiopathic Hypoparathyroidism A condition of low or absent PTH level and HYPOCALCEMIA. It usually occurs as part of an autoimmune syndrome. | 0 | 2.06 | 1 | 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 | 2.06 | 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 | 3.34 | 2 | 0 |
Ductal Carcinoma [description not available] | 0 | 2.07 | 1 | 0 |
Carcinoma, Ductal Malignant neoplasms involving the ductal systems of any of a number of organs, such as the MAMMARY GLANDS, the PANCREAS, the PROSTATE, or the LACRIMAL GLAND. | 0 | 2.07 | 1 | 0 |
Corneal Dystrophies [description not available] | 0 | 2.06 | 1 | 0 |
Arm Injuries General or unspecified injuries involving the UPPER ARM and the FOREARM. | 0 | 2.68 | 3 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 2.06 | 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 | 2.06 | 1 | 0 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 2.69 | 3 | 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 | 2.69 | 3 | 0 |
Encephalopathy, Hepatic [description not available] | 0 | 4.07 | 3 | 1 |
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 | 4.07 | 3 | 1 |
Cantrell Haller Ravitch syndrome [description not available] | 0 | 2.06 | 1 | 0 |
Cancer of Oropharnyx [description not available] | 0 | 2.07 | 1 | 0 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 2.07 | 1 | 0 |
Cancer of Eye [description not available] | 0 | 4.9 | 14 | 0 |
Tracheal Stenosis A pathological narrowing of the TRACHEA. | 0 | 4.74 | 12 | 0 |
Panic Attacks [description not available] | 0 | 3.46 | 1 | 1 |
Panic Disorder A type of anxiety disorder characterized by unexpected panic attacks that last minutes or, rarely, hours. Panic attacks begin with intense apprehension, fear or terror and, often, a feeling of impending doom. Symptoms experienced during a panic attack include dyspnea or sensations of being smothered; dizziness, loss of balance or faintness; choking sensations; palpitations or accelerated heart rate; shakiness; sweating; nausea or other form of abdominal distress; depersonalization or derealization; paresthesias; hot flashes or chills; chest discomfort or pain; fear of dying and fear of not being in control of oneself or going crazy. Agoraphobia may also develop. Similar to other anxiety disorders, it may be inherited as an autosomal dominant trait. | 0 | 3.46 | 1 | 1 |
Alopecia Mucinosa [description not available] | 0 | 2.99 | 1 | 0 |
Encephalopathy, Toxic [description not available] | 0 | 2.07 | 1 | 0 |
Maculopapular Cutaneous Mastocytosis [description not available] | 0 | 2.38 | 2 | 0 |
Adult Periodontitis [description not available] | 0 | 2.07 | 1 | 0 |
Pocket, Periodontal [description not available] | 0 | 2.07 | 1 | 0 |
Periodontal Pocket An abnormal extension of a gingival sulcus accompanied by the apical migration of the epithelial attachment and bone resorption. | 0 | 2.07 | 1 | 0 |
Allergic Bronchopulmonary Aspergilloses [description not available] | 0 | 2.07 | 1 | 0 |
Aspergillosis, Allergic Bronchopulmonary Hypersensitivity reaction (ALLERGIC REACTION) to fungus ASPERGILLUS in an individual with long-standing BRONCHIAL ASTHMA. It is characterized by pulmonary infiltrates, EOSINOPHILIA, elevated serum IMMUNOGLOBULIN E, and skin reactivity to Aspergillus antigen. | 0 | 2.07 | 1 | 0 |
Myxoma, Nerve Sheath [description not available] | 0 | 2.07 | 1 | 0 |
Allergy, Peanut [description not available] | 0 | 3.83 | 2 | 1 |
Peanut Hypersensitivity Allergic reaction to peanuts that is triggered by the immune system. | 0 | 3.83 | 2 | 1 |
Mastitis INFLAMMATION of the BREAST, or MAMMARY GLAND. | 0 | 2.66 | 3 | 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 | 2.07 | 1 | 0 |
Bowel Diseases, Inflammatory [description not available] | 0 | 2.07 | 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 | 2.07 | 1 | 0 |
Actinobacillus Infections Infections with bacteria of the genus ACTINOBACILLUS. | 0 | 4.16 | 6 | 0 |
Adenolymphoma A benign tumor characterized histologically by tall columnar epithelium within a lymphoid tissue stroma. It is usually found in the salivary glands, especially the parotid. | 0 | 2.07 | 1 | 0 |
Cancer of Parotid [description not available] | 0 | 4.27 | 7 | 0 |
Parotid Neoplasms Tumors or cancer of the PAROTID GLAND. | 0 | 4.27 | 7 | 0 |
Human T-lymphotropic Virus 1 Infection [description not available] | 0 | 2.07 | 1 | 0 |
HTLV-I Infections Diseases caused by HUMAN T-LYMPHOTROPIC VIRUS 1. | 0 | 2.07 | 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 | 3.46 | 8 | 0 |
Astasia-Abasia [description not available] | 0 | 2.38 | 2 | 0 |
Bladder Disorder, Neurogenic [description not available] | 0 | 2.99 | 1 | 0 |
Paralysis, Legs [description not available] | 0 | 3.59 | 3 | 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 | 2.99 | 1 | 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 | 3.59 | 3 | 0 |
Pulmonary Stenoses [description not available] | 0 | 2.68 | 3 | 0 |
Leprosy, Macular [description not available] | 0 | 2.07 | 1 | 0 |
Leprosy, Borderline A form of LEPROSY in which there are clinical manifestations of both principal types (lepromatous and tuberculoid). The disease may shift toward one of these two polar or principal forms. | 0 | 2.44 | 2 | 0 |
Cardiac Septal Defect [description not available] | 0 | 2.07 | 1 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 2.71 | 3 | 0 |
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 | 2.71 | 3 | 0 |
Tooth Discoloration Any change in the hue, color, or translucency of a tooth due to any cause. Restorative filling materials, drugs (both topical and systemic), pulpal necrosis, or hemorrhage may be responsible. (Jablonski, Dictionary of Dentistry, 1992, p253) | 0 | 2.37 | 2 | 0 |
Anemia, Cooley's [description not available] | 0 | 2.42 | 2 | 0 |
Gingivitis Inflammation of gum tissue (GINGIVA) without loss of connective tissue. | 0 | 2.07 | 1 | 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 | 2.42 | 2 | 0 |
Joint Pain [description not available] | 0 | 2.1 | 1 | 0 |
Arthralgia Pain in the joint. | 0 | 2.1 | 1 | 0 |
Leukemia, Megakaryocytic [description not available] | 0 | 2.07 | 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 | 2.07 | 1 | 0 |
Bruxism, Nocturnal [description not available] | 0 | 2.44 | 2 | 0 |
Paraganglioma, Gangliocytic [description not available] | 0 | 3.33 | 2 | 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 | 3.33 | 2 | 0 |
Myofascial Trigger Point Pain [description not available] | 0 | 2.08 | 1 | 0 |
Myofascial Pain Syndromes Muscular pain in numerous body regions that can be reproduced by pressure on TRIGGER POINTS, localized hardenings in skeletal muscle tissue. Pain is referred to a location distant from the trigger points. A prime example is the TEMPOROMANDIBULAR JOINT DYSFUNCTION SYNDROME. | 0 | 2.08 | 1 | 0 |
Pycnodysostosis Rare autosomal recessive syndrome characterized by delayed closing of CRANIAL SUTURES, short stature, ACRO-OSTEOLYSIS of distal phalanges, dental and MAXILLOFACIAL ABNORMALITIES and an increase in bone density that results in frequent BONE FRACTURES. It is associated with BONE RESORPTION defect due to mutations in the lysosomal cysteine protease CATHEPSIN K. | 0 | 2.08 | 1 | 0 |
Cleidocranial Digital Dysostosis [description not available] | 0 | 2.08 | 1 | 0 |
Cirrhosis, Liver [description not available] | 0 | 3.77 | 2 | 1 |
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 | 3.77 | 2 | 1 |
Apple Peel Small Bowel Syndrome [description not available] | 0 | 3.8 | 4 | 0 |
Hydrophobia [description not available] | 0 | 3.23 | 6 | 0 |
Deficiency, Factor 11 [description not available] | 0 | 2.07 | 1 | 0 |
Neoplasms, Otorhinolaryngologic [description not available] | 0 | 4.72 | 2 | 1 |
Chondrodystrophic Myotonia [description not available] | 0 | 5.07 | 10 | 0 |
Basedow Disease [description not available] | 0 | 3.1 | 5 | 0 |
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 | 3.1 | 5 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 2.38 | 2 | 0 |
Tooth Fractures Break or rupture of a tooth or tooth root. | 0 | 2.9 | 4 | 0 |
Alogia [description not available] | 0 | 2.01 | 1 | 0 |
Age-Related Memory Disorders [description not available] | 0 | 2.41 | 2 | 0 |
Brain Hemorrhage, Cerebral, Traumatic [description not available] | 0 | 2.01 | 1 | 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 | 2.01 | 1 | 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 | 2.41 | 2 | 0 |
Vaccinia The cutaneous and occasional systemic reactions associated with vaccination using smallpox (variola) vaccine. | 0 | 2.89 | 4 | 0 |
Infections, Retroviridae [description not available] | 0 | 2.01 | 1 | 0 |
Fibroma, Shope [description not available] | 0 | 2.7 | 3 | 0 |
Retroviridae Infections Virus diseases caused by the RETROVIRIDAE. | 0 | 2.01 | 1 | 0 |
Bile Duct Diseases Diseases in any part of the ductal system of the BILIARY TRACT from the smallest BILE CANALICULI to the largest COMMON BILE DUCT. | 0 | 2.69 | 3 | 0 |
Gallstone Disease [description not available] | 0 | 2.4 | 2 | 0 |
Cholelithiasis Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). | 0 | 2.4 | 2 | 0 |
Mandibular Diseases Diseases involving the MANDIBLE. | 0 | 3.21 | 6 | 0 |
Experimental Leukemia [description not available] | 0 | 2.38 | 2 | 0 |
Frambesia [description not available] | 0 | 2.64 | 3 | 0 |
Yaws A systemic non-venereal infection of the tropics caused by TREPONEMA PALLIDUM subspecies pertenue. | 0 | 2.64 | 3 | 0 |
Contact Dermatitis [description not available] | 0 | 2.38 | 2 | 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 | 2.38 | 2 | 0 |
Chronic Primary Open Angle Glaucoma [description not available] | 0 | 2.39 | 2 | 0 |
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 | 2.39 | 2 | 0 |
Briquet Syndrome [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Trichotillomania Compulsion to pull out one's hair. | 0 | 2.41 | 2 | 0 |
Delayed Hypersensitivity [description not available] | 0 | 6.37 | 11 | 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 | 2.01 | 1 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 2.38 | 2 | 0 |
Malignancies, Post-Traumatic [description not available] | 0 | 2.01 | 1 | 0 |
Granuloma Gangraenescens [description not available] | 0 | 5.94 | 26 | 0 |
Granulomatosis, Lymphomatoid [description not available] | 0 | 2.38 | 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 | 5.94 | 26 | 0 |
Cerebrospinal Fluid Otorrhea Discharge of cerebrospinal fluid through the external auditory meatus or through the eustachian tube into the nasopharynx. This is usually associated with CRANIOCEREBRAL TRAUMA (e.g., SKULL FRACTURE involving the TEMPORAL BONE;), NEUROSURGICAL PROCEDURES; or other conditions, but may rarely occur spontaneously. (From Am J Otol 1995 Nov;16(6):765-71) | 0 | 2.72 | 3 | 0 |
Klein Syndrome [description not available] | 0 | 4.03 | 15 | 0 |
DNA Virus Infections Diseases caused by DNA VIRUSES. | 0 | 3.81 | 2 | 1 |
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 | 3.56 | 9 | 0 |
Cardiovascular Pregnancy Complications [description not available] | 0 | 3.58 | 3 | 0 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 3.56 | 9 | 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 | 2.01 | 1 | 0 |
Hyphema Bleeding in the anterior chamber of the eye. | 0 | 2.01 | 1 | 0 |
Drug-Induced Stevens Johnson Syndrome [description not available] | 0 | 3.58 | 3 | 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 | 3.58 | 3 | 0 |
Gait Disorders, Animal [description not available] | 0 | 2.01 | 1 | 0 |
Neuroectodermal Tumors Malignant neoplasms arising in the neuroectoderm, the portion of the ectoderm of the early embryo that gives rise to the central and peripheral nervous systems, including some glial cells. | 0 | 2.01 | 1 | 0 |
Diverticula [description not available] | 0 | 2.4 | 2 | 0 |
Digestive System Disorders [description not available] | 0 | 7.07 | 4 | 3 |
Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | 0 | 7.07 | 4 | 3 |
Benign Essential Tremor [description not available] | 0 | 2.42 | 2 | 0 |
Dyskinesia Syndromes [description not available] | 0 | 3.07 | 5 | 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 | 3.07 | 5 | 0 |
Essential Tremor A relatively common disorder characterized by a fairly specific pattern of tremors which are most prominent in the upper extremities and neck, inducing titubations of the head. The tremor is usually mild, but when severe may be disabling. An autosomal dominant pattern of inheritance may occur in some families (i.e., familial tremor). (Mov Disord 1988;13(1):5-10) | 0 | 2.42 | 2 | 0 |
Atypical Lipomatous Tumor [description not available] | 0 | 2.38 | 2 | 0 |
Liposarcoma A malignant tumor derived from primitive or embryonal lipoblastic cells. It may be composed of well-differentiated fat cells or may be dedifferentiated: myxoid (LIPOSARCOMA, MYXOID), round-celled, or pleomorphic, usually in association with a rich network of capillaries. Recurrences are common and dedifferentiated liposarcomas metastasize to the lungs or serosal surfaces. (From Dorland, 27th ed; Stedman, 25th ed) | 0 | 2.38 | 2 | 0 |
Benign Mucosal Pemphigoid [description not available] | 0 | 2.01 | 1 | 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 | 2.01 | 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 | 3.99 | 5 | 0 |
Chancre The primary sore of syphilis, a painless indurated, eroded papule, occurring at the site of entry of the infection. | 0 | 2.35 | 2 | 0 |
Essential Polyarteritis [description not available] | 0 | 3.18 | 6 | 0 |
Adenofibroma A benign neoplasm composed of glandular and fibrous tissues, with a relatively large proportion of glands. (Stedman, 25th ed) | 0 | 1.93 | 1 | 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 | 4.58 | 6 | 1 |
Infectious Myelitis [description not available] | 0 | 1.93 | 1 | 0 |
Fractures, Compound [description not available] | 0 | 1.93 | 1 | 0 |
Centriacinar Emphysema [description not available] | 0 | 5.28 | 7 | 2 |
Rheumatism [description not available] | 0 | 2.62 | 3 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 2.62 | 3 | 0 |
Polyarthritis [description not available] | 0 | 3.19 | 6 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 3.19 | 6 | 0 |
Osseous Paget's Disease [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Female Genital Diseases [description not available] | 0 | 5.16 | 4 | 1 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 5.16 | 4 | 1 |
Francisella tularensis Infection [description not available] | 0 | 2.34 | 2 | 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 | 2.34 | 2 | 0 |
Neoplasms, Nerve Sheath [description not available] | 0 | 1.93 | 1 | 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 | 1.93 | 1 | 0 |
Congenital Syphilis [description not available] | 0 | 2.85 | 4 | 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 | 2.85 | 4 | 0 |
Parotiditis [description not available] | 0 | 1.93 | 1 | 0 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 3.78 | 4 | 0 |
Nevi, Intradermal [description not available] | 0 | 2.85 | 4 | 0 |
Nevus, Epithelioid and Spindle Cell A benign compound nevus occurring most often in children before puberty, composed of spindle and epithelioid cells located mainly in the dermis, sometimes in association with large atypical cells and multinucleate cells, and having a close histopathological resemblance to malignant melanoma. The tumor presents as a smooth to slightly scaly, round to oval, raised, firm papule or nodule, ranging in color from pink-tan to purplish red, often with surface telangiectasia. (Dorland, 27th ed) | 0 | 3.04 | 5 | 0 |
Blue Nevi [description not available] | 0 | 3.04 | 5 | 0 |
Depression, Endogenous [description not available] | 0 | 3.03 | 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 | 3.03 | 5 | 0 |
Respiratory Tract Neoplasms New abnormal growth of tissue in the RESPIRATORY SYSTEM. | 0 | 3.95 | 14 | 0 |
Foreign-Body Reaction Chronic inflammation and granuloma formation around irritating foreign bodies. | 0 | 4.76 | 12 | 0 |
Blepharospasm Excessive winking; tonic or clonic spasm of the orbicularis oculi muscle. | 0 | 2.36 | 2 | 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 | 2.34 | 2 | 0 |
Acquired Meningomyelocele [description not available] | 0 | 2.34 | 2 | 0 |
Cleft Spine [description not available] | 0 | 2.63 | 3 | 0 |
Cancer of the Tonsil [description not available] | 0 | 2.86 | 4 | 0 |
Tonsillar Neoplasms Tumors or cancer of the PALATINE TONSIL. | 0 | 2.86 | 4 | 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 | 3.03 | 5 | 0 |
Pneumoperitoneum A condition with trapped gas or air in the PERITONEAL CAVITY, usually secondary to perforation of the internal organs such as the LUNG and the GASTROINTESTINAL TRACT, or to recent surgery. Pneumoperitoneum may be purposely introduced to aid radiological examination. | 0 | 2.34 | 2 | 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 | 1.93 | 1 | 0 |
Chilblains Recurrent localized itching, swelling and painful erythema on the fingers, toes or ears, produced by exposure to cold. | 0 | 2.36 | 2 | 0 |
Angiohemophilia [description not available] | 0 | 1.93 | 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 | 1.93 | 1 | 0 |
Mucositis, Oral [description not available] | 0 | 3.96 | 5 | 0 |
Stomatitis INFLAMMATION of the soft tissues of the MOUTH, such as MUCOSA; PALATE; GINGIVA; and LIP. | 0 | 3.96 | 5 | 0 |
Tuberculoma A tumor-like mass resulting from the enlargement of a tuberculous lesion. | 0 | 2.62 | 3 | 0 |
Postintubation Croup [description not available] | 0 | 3.2 | 6 | 0 |
Croup Inflammation involving the GLOTTIS or VOCAL CORDS and the subglottic larynx. Croup is characterized by a barking cough, HOARSENESS, and persistent inspiratory STRIDOR (a high-pitched breathing sound). It occurs chiefly in infants and children. | 0 | 3.2 | 6 | 0 |
Gangliocytoma [description not available] | 0 | 2.34 | 2 | 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 | 2.35 | 2 | 0 |
Infections, Trichomonas [description not available] | 0 | 1.93 | 1 | 0 |
Trichomonas Infections Infections in birds and mammals produced by various species of Trichomonas. | 0 | 1.93 | 1 | 0 |
Reproductive Sterility [description not available] | 0 | 1.93 | 1 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 1.93 | 1 | 0 |
Rhabdomyosarcoma, Embryonal A form of RHABDOMYOSARCOMA arising primarily in the head and neck, especially the orbit, of children below the age of 10. The cells are smaller than those of other rhabdomyosarcomas and are of two basic cell types: spindle cells and round cells. This cancer is highly sensitive to chemotherapy and has a high cure rate with multi-modality therapy. (From Holland et al., Cancer Medicine, 3d ed, p2188) | 0 | 1.93 | 1 | 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 | 2.34 | 2 | 0 |
Myoepithelial Tumor [description not available] | 0 | 2.36 | 2 | 0 |
Myoepithelioma A usually benign tumor made up predominantly of myoepithelial cells. | 0 | 2.36 | 2 | 0 |
Absence Seizure [description not available] | 0 | 3.34 | 7 | 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 | 3.34 | 7 | 0 |
Multiple Neurofibromas [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Hydramnios [description not available] | 0 | 1.93 | 1 | 0 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 2.64 | 3 | 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 | 2.64 | 3 | 0 |
Allergy, Food [description not available] | 0 | 3.46 | 8 | 0 |
Food Hypersensitivity Gastrointestinal disturbances, skin eruptions, or shock due to allergic reactions to allergens in food. | 0 | 3.46 | 8 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 3.04 | 5 | 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 | 3.04 | 5 | 0 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 1.93 | 1 | 0 |
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 | 1.93 | 1 | 0 |
Gastroduodenal Ulcer [description not available] | 0 | 2.33 | 2 | 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 | 2.33 | 2 | 0 |
Splenic Diseases Diseases involving the SPLEEN. | 0 | 1.93 | 1 | 0 |
Choked Disk [description not available] | 0 | 2.34 | 2 | 0 |
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 | 2.34 | 2 | 0 |
Salivary Gland Fistula A fistula between a salivary duct or gland and the cutaneous surface of the oral cavity. | 0 | 2.34 | 2 | 0 |
Deafness, Sudden Complete sensorineural hearing loss which develops suddenly over a period of hours or a few days. | 0 | 1.93 | 1 | 0 |
Cardiac Death [description not available] | 0 | 2.86 | 4 | 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 | 2.64 | 3 | 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 | 2.64 | 3 | 0 |
Peripheral Nerve Injury [description not available] | 0 | 1.93 | 1 | 0 |
Peripheral Nerve Injuries Injuries to the PERIPHERAL NERVES. | 0 | 1.93 | 1 | 0 |
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 | 2.35 | 2 | 0 |
Keratoconjunctivitis Simultaneous inflammation of the cornea and conjunctiva. | 0 | 4.11 | 6 | 0 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 3.04 | 5 | 0 |
Infection, Toxoplasma gondii [description not available] | 0 | 2.34 | 2 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 2.34 | 2 | 0 |
Actinic Reticuloid Syndrome [description not available] | 0 | 3.05 | 5 | 0 |
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 | 3.21 | 6 | 0 |
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 |
Hemoptysis Expectoration or spitting of blood originating from any part of the RESPIRATORY TRACT, usually from hemorrhage in the lung parenchyma (PULMONARY ALVEOLI) and the BRONCHIAL ARTERIES. | 0 | 1.93 | 1 | 0 |
Auditory Vertigo [description not available] | 0 | 2.63 | 3 | 0 |
Peritoneal Diseases Pathological processes involving the PERITONEUM. | 0 | 1.93 | 1 | 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 | 2.63 | 3 | 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 | 2.35 | 2 | 0 |
Angor Pectoris [description not available] | 0 | 1.93 | 1 | 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 | 1.93 | 1 | 0 |
Focal Neurologic Deficits [description not available] | 0 | 3.19 | 6 | 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 | 2.85 | 4 | 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 | 2.34 | 2 | 0 |
Leukocyte Disorders Disordered formation of various types of leukocytes or an abnormal accumulation or deficiency of these cells. | 0 | 1.93 | 1 | 0 |
Dentigerous Cyst Most common follicular odontogenic cyst. Occurs in relation to a partially erupted or unerupted tooth with at least the crown of the tooth to which the cyst is attached protruding into the cystic cavity. May give rise to an ameloblastoma and, in rare instances, undergo malignant transformation. | 0 | 3.95 | 5 | 0 |
Fracture Malunion [description not available] | 0 | 1.93 | 1 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 3.03 | 5 | 0 |
Infection, Puerperal [description not available] | 0 | 2.34 | 2 | 0 |
Inner Ear Disease [description not available] | 0 | 3.05 | 5 | 0 |
Labyrinth Diseases Pathological processes of the inner ear (LABYRINTH) which contains the essential apparatus of hearing (COCHLEA) and balance (SEMICIRCULAR CANALS). | 0 | 3.05 | 5 | 0 |
Eye Manifestations Ocular disorders attendant upon non-ocular disease or injury. | 0 | 4.94 | 9 | 0 |
Vaginitis Inflammation of the vagina characterized by pain and a purulent discharge. | 0 | 2.64 | 3 | 0 |
Claustrophobia [description not available] | 0 | 2.35 | 2 | 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 | 2.35 | 2 | 0 |
Paronychia An inflammatory reaction involving the folds of the skin surrounding the fingernail. It is characterized by acute or chronic purulent, tender, and painful swellings of the tissues around the nail, caused by an abscess of the nail fold. The pathogenic yeast causing paronychia is most frequently Candida albicans. Saprophytic fungi may also be involved. The causative bacteria are usually Staphylococcus, Pseudomonas aeruginosa, or Streptococcus. (Andrews' Diseases of the Skin, 8th ed, p271) | 0 | 1.93 | 1 | 0 |
Hyaline Membrane Disease A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS). | 0 | 2.86 | 4 | 0 |
Cephalgia, Vascular [description not available] | 0 | 3.79 | 4 | 0 |
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 | 3.78 | 4 | 0 |
Diverticula, Esophageal [description not available] | 0 | 2.37 | 2 | 0 |
Fibromatosis Gingivae [description not available] | 0 | 4.14 | 6 | 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 | 2.36 | 2 | 0 |
Aneurysm, Arteriovenous [description not available] | 0 | 4.13 | 6 | 0 |
Anterior Optic Neuritis [description not available] | 0 | 2.85 | 4 | 0 |
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 | 2.85 | 4 | 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 | 5.73 | 21 | 1 |
Hydrosyringomyelia [description not available] | 0 | 1.94 | 1 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 2.36 | 2 | 0 |
Air Embolism [description not available] | 0 | 2.36 | 2 | 0 |
Bronchospasm [description not available] | 0 | 5.66 | 7 | 1 |
Bronchial Spasm Spasmodic contraction of the smooth muscle of the bronchi. | 0 | 5.66 | 7 | 1 |
Laryngeal Tuberculosis [description not available] | 0 | 3.56 | 3 | 0 |
Erythrocytosis [description not available] | 0 | 3.26 | 2 | 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 | 2.64 | 3 | 0 |
Anomalous Dysplasia of Dentin [description not available] | 0 | 1.94 | 1 | 0 |
Dental Tissue Neoplasms [description not available] | 0 | 2.36 | 2 | 0 |
Abrasion, Dental [description not available] | 0 | 2.64 | 3 | 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 |
Brachmann-De Lange Syndrome [description not available] | 0 | 2.35 | 2 | 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 | 2.35 | 2 | 0 |
Flatus [description not available] | 0 | 4.94 | 3 | 1 |
Muscle Spasm [description not available] | 0 | 2.64 | 3 | 0 |
Flatulence Production or presence of gas in the gastrointestinal tract which may be expelled through the anus. | 0 | 4.94 | 3 | 1 |
Spasm An involuntary contraction of a muscle or group of muscles. Spasms may involve SKELETAL MUSCLE or SMOOTH MUSCLE. | 0 | 2.64 | 3 | 0 |
Foot Diseases Anatomical and functional disorders affecting the foot. | 0 | 2.87 | 4 | 0 |
Finger Injuries General or unspecified injuries involving the fingers. | 0 | 3.57 | 9 | 0 |
Hypogalactia A condition of less than normal MILK secretion. | 0 | 2.85 | 4 | 0 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 1.94 | 1 | 0 |
Fractures, Ununited A fracture in which union fails to occur, the ends of the bone becoming rounded and eburnated, and a false joint occurs. (Stedman, 25th ed) | 0 | 2.34 | 2 | 0 |
Gastric Ulcer [description not available] | 0 | 2.87 | 4 | 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 | 2.87 | 4 | 0 |
Meniscitis [description not available] | 0 | 3.05 | 5 | 0 |
Thrombocytopathy [description not available] | 0 | 1.94 | 1 | 0 |
Christmas Disease [description not available] | 0 | 2.37 | 2 | 0 |
Blood Platelet Disorders Disorders caused by abnormalities in platelet count or function. | 0 | 1.94 | 1 | 0 |
Hemophilia B A deficiency of blood coagulation factor IX inherited as an X-linked disorder. (Also known as Christmas Disease, after the first patient studied in detail, not the holy day.) Historical and clinical features resemble those in classic hemophilia (HEMOPHILIA A), but patients present with fewer symptoms. Severity of bleeding is usually similar in members of a single family. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma. Treatment is similar to that for hemophilia A. (From Cecil Textbook of Medicine, 19th ed, p1008) | 0 | 2.37 | 2 | 0 |
46, XY Disorders of Sex Development [description not available] | 0 | 1.94 | 1 | 0 |
Pyloric Stenosis Narrowing of the pyloric canal with varied etiology. A common form is due to muscle hypertrophy (PYLORIC STENOSIS, HYPERTROPHIC) seen in infants. | 0 | 2.64 | 3 | 0 |
Hypospadias A birth defect due to malformation of the URETHRA in which the urethral opening is below its normal location. In the male, the malformed urethra generally opens on the ventral surface of the PENIS or on the PERINEUM. In the female, the malformed urethral opening is in the VAGINA. | 0 | 5.05 | 7 | 0 |
Skin Manifestations Dermatologic disorders attendant upon non-dermatologic disease or injury. | 0 | 3.96 | 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 | 2.35 | 2 | 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 | 1.94 | 1 | 0 |
Measles, German [description not available] | 0 | 7.94 | 19 | 5 |
Bilirubin Encephalopathy [description not available] | 0 | 1.94 | 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 | 2.35 | 2 | 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 | 1.94 | 1 | 0 |
Burning Mouth Syndrome A group of painful oral symptoms associated with a burning or similar sensation. There is usually a significant organic component with a degree of functional overlay; it is not limited to the psychophysiologic group of disorders. | 0 | 1.94 | 1 | 0 |
Abnormalities, Severe Teratoid Marked developmental anomalies of a fetus or infant. | 0 | 3.82 | 12 | 0 |
Fulminant Meningococcal Sepsis with Adrenal Apoplexy [description not available] | 0 | 1.93 | 1 | 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 | 1.93 | 1 | 0 |
Dermal Sinus [description not available] | 0 | 2.36 | 2 | 0 |
Hyperkyphosis [description not available] | 0 | 2.35 | 2 | 0 |
Menstruation, Painful [description not available] | 0 | 1.93 | 1 | 0 |
Dysmenorrhea Painful menstruation. | 0 | 1.93 | 1 | 0 |
Algodystrophic Syndrome [description not available] | 0 | 1.93 | 1 | 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 | 1.93 | 1 | 0 |
Scarlet Fever Infection with group A streptococci that is characterized by tonsillitis and pharyngitis. An erythematous rash is commonly present. | 0 | 2.64 | 3 | 0 |
Poland Anomaly [description not available] | 0 | 3.6 | 3 | 0 |
Enuresis Involuntary discharge of URINE after expected age of completed development of urinary control. This can happen during the daytime (DIURNAL ENURESIS) while one is awake or during sleep (NOCTURNAL ENURESIS). Enuresis can be in children or in adults (as persistent primary enuresis and secondary adult-onset enuresis). | 0 | 2.93 | 1 | 0 |
Attention Deficit and Disruptive Behavioral Disorders [description not available] | 0 | 2.93 | 1 | 0 |
Attention Deficit and Disruptive Behavior Disorders Includes two similar disorders: oppositional defiant disorder and CONDUCT DISORDERS. Symptoms occurring in children with these disorders include: defiance of authority figures, angry outbursts, and other antisocial behaviors. | 0 | 2.93 | 1 | 0 |
Atypical Cluster Headache [description not available] | 0 | 3.09 | 5 | 0 |
Osteoarthritis of Knee [description not available] | 0 | 2.01 | 1 | 0 |
Osteoarthritis, Knee Noninflammatory degenerative disease of the knee joint consisting of three large categories: conditions that block normal synchronous movement, conditions that produce abnormal pathways of motion, and conditions that cause stress concentration resulting in changes to articular cartilage. (Crenshaw, Campbell's Operative Orthopaedics, 8th ed, p2019) | 0 | 2.01 | 1 | 0 |
Abscess, Periapical [description not available] | 0 | 2.37 | 2 | 0 |
Bowen Disease [description not available] | 0 | 2.01 | 1 | 0 |
Parasitic Skin Diseases [description not available] | 0 | 2.43 | 2 | 0 |
Hemisensory Neglect [description not available] | 0 | 2.37 | 2 | 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 | 2.37 | 2 | 0 |
Abdominal Pregnancy [description not available] | 0 | 1.92 | 1 | 0 |
Ectopic Pregnancy [description not available] | 0 | 1.92 | 1 | 0 |
Pregnancy, Ectopic A potentially life-threatening condition in which EMBRYO IMPLANTATION occurs outside the cavity of the UTERUS. Most ectopic pregnancies ( | 0 | 1.92 | 1 | 0 |
Otospongiosis [description not available] | 0 | 2.35 | 2 | 0 |
Otosclerosis Formation of spongy bone in the labyrinth capsule which can progress toward the STAPES (stapedial fixation) or anteriorly toward the COCHLEA leading to conductive, sensorineural, or mixed HEARING LOSS. Several genes are associated with familial otosclerosis with varied clinical signs. | 0 | 2.35 | 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 |
Mesenchymoma A mixed mesenchymal tumor composed of two or more mesodermal cellular elements not commonly associated, not counting fibrous tissue as one of the elements. Mesenchymomas are widely distributed in the body and about 75% are malignant. (Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1866) | 0 | 2.64 | 3 | 0 |
Acantholytic Dyskeratotic Epidermal Nevi [description not available] | 0 | 2.34 | 2 | 0 |
Bigfoot Disease [description not available] | 0 | 1.92 | 1 | 0 |
Peripheral Nerve Neoplasms [description not available] | 0 | 2.34 | 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 | 2.34 | 2 | 0 |
Osteitis Fibrosa Cystica A fibrous degeneration, cyst formation, and the presence of fibrous nodules in bone, usually due to HYPERPARATHYROIDISM. | 0 | 2.34 | 2 | 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 | 1.92 | 1 | 0 |
Adamantinoma A locally aggressive, osteolytic neoplasm of the long bones, probably of epithelial origin and most often involving the TIBIA. | 0 | 1.92 | 1 | 0 |
Adenoma Sebaceum Facial ANGIOFIBROMA in tuberous sclerosis | 0 | 1.92 | 1 | 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 | 1.92 | 1 | 0 |
Serositis Inflammation of a serous membrane. | 0 | 1.93 | 1 | 0 |
Avitaminosis A condition due to a deficiency of one or more essential vitamins. (Dorland, 27th ed) | 0 | 1.93 | 1 | 0 |
Hyperthyroid [description not available] | 0 | 3.27 | 2 | 0 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 3.27 | 2 | 0 |
Acute Onset Aura Migraine [description not available] | 0 | 2.02 | 1 | 0 |
Flushing A transient reddening of the face that may be due to fever, certain drugs, exertion, or stress. | 0 | 2.69 | 3 | 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 | 2.02 | 1 | 0 |
Syringoma A benign tumor of the sweat glands which is usually multiple and results from malformation of sweat ducts. It is uncommon and more common in females than in males. It is most likely to appear at adolescence, and further lesions may develop during adult life. It does not appear to be hereditary. (Rook et al., Textbook of Dermatology, 4th ed, pp2407-8) | 0 | 2.93 | 1 | 0 |
Gastric Rupture [description not available] | 0 | 2.02 | 1 | 0 |
Anochlesia [description not available] | 0 | 2.02 | 1 | 0 |
Neoplasm Metastasis, Unknown Primary [description not available] | 0 | 2.02 | 1 | 0 |
Adenoma, Sweat Gland A benign neoplasm derived from epithelial cells of sweat glands. (Stedman, 25th ed) | 0 | 2.4 | 2 | 0 |
Inflammatory Response Syndrome, Systemic [description not available] | 0 | 3.81 | 2 | 1 |
Systemic Inflammatory Response Syndrome A systemic inflammatory response to a variety of clinical insults, characterized by two or more of the following conditions: (1) fever | 0 | 3.81 | 2 | 1 |
Impotence [description not available] | 0 | 4.06 | 3 | 1 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 4.06 | 3 | 1 |
Mycoplasma dispar Infection [description not available] | 0 | 2.94 | 4 | 0 |
Respiratory Syndrome, Acute, Severe [description not available] | 0 | 2.02 | 1 | 0 |
Severe Acute Respiratory Syndrome A viral disorder characterized by high FEVER, dry COUGH, shortness of breath (DYSPNEA) or breathing difficulties, and atypical PNEUMONIA. A virus in the genus CORONAVIRUS is the suspected agent. | 0 | 2.02 | 1 | 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 | 3.39 | 7 | 0 |
Failure to Thrive A condition of substandard growth or diminished capacity to maintain normal function. | 0 | 4.95 | 6 | 0 |
Fasting Hypoglycemia HYPOGLYCEMIA expressed in the postabsorptive state, after prolonged FASTING, or an overnight fast. | 0 | 2.02 | 1 | 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 | 2.02 | 1 | 0 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 2.64 | 3 | 0 |
Autoimmune Thrombocytopenia [description not available] | 0 | 2.35 | 2 | 0 |
Purpura, Thrombopenic [description not available] | 0 | 1.92 | 1 | 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 | 2.64 | 3 | 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 | 1.92 | 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 | 2.35 | 2 | 0 |
Phimosis A condition in which the FORESKIN cannot be retracted to reveal the GLANS PENIS. It is due to tightness or narrowing of the foreskin opening. | 0 | 1.92 | 1 | 0 |
Anogenital Type Verrucous Carcinoma [description not available] | 0 | 1.92 | 1 | 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 |
Lichen Ruber Planus [description not available] | 0 | 2.02 | 1 | 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 | 2.02 | 1 | 0 |
Injuries, Leg [description not available] | 0 | 3.79 | 4 | 0 |
Hiccough [description not available] | 0 | 2.02 | 1 | 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 | 2.94 | 1 | 0 |
Charcot-Marie-Tooth Disease, Demyelinating, Type 4f [description not available] | 0 | 3.4 | 1 | 1 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 4.31 | 4 | 0 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 5.01 | 5 | 2 |
Convergent Strabismus [description not available] | 0 | 3.81 | 4 | 0 |
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 | 3.81 | 4 | 0 |
Human Adenovirus Infections [description not available] | 0 | 2.4 | 2 | 0 |
Adenovirus Infections, Human Respiratory and conjunctival infections caused by 33 identified serotypes of human adenoviruses. | 0 | 2.4 | 2 | 0 |
Hemorrhagic Shock [description not available] | 0 | 2.37 | 2 | 0 |
Drop Attack [description not available] | 0 | 2.39 | 2 | 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 | 2.39 | 2 | 0 |
Burns, Electric Burns produced by contact with electric current or from a sudden discharge of electricity. | 0 | 2.39 | 2 | 0 |
CKD-MBD [description not available] | 0 | 2.02 | 1 | 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 | 2.37 | 2 | 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 | 2.02 | 1 | 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 | 2.41 | 2 | 0 |
Esophagitis INFLAMMATION, acute or chronic, of the ESOPHAGUS caused by BACTERIA, chemicals, or TRAUMA. | 0 | 2.02 | 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 | 2.02 | 1 | 0 |
Sterility, Female [description not available] | 0 | 2.41 | 2 | 0 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 2.41 | 2 | 0 |
Dandy-Walker Complex [description not available] | 0 | 3.32 | 2 | 0 |
Double Tooth [description not available] | 0 | 2.02 | 1 | 0 |
Mitral Incompetence [description not available] | 0 | 2.02 | 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 | 2.02 | 1 | 0 |
Arachnoid Cysts Intracranial or spinal cavities containing a cerebrospinal-like fluid, the wall of which is composed of arachnoidal cells. They are most often developmental or related to trauma. Intracranial arachnoid cysts usually occur adjacent to arachnoidal cistern and may present with HYDROCEPHALUS; HEADACHE; SEIZURES; and focal neurologic signs. (From Joynt, Clinical Neurology, 1994, Ch44, pp105-115) | 0 | 2.42 | 2 | 0 |
Cerebral Palsy, Athetoid [description not available] | 0 | 2.02 | 1 | 0 |
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 | 2.02 | 1 | 0 |
Actinomycetoma [description not available] | 0 | 2.66 | 3 | 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 | 2.66 | 3 | 0 |
Muscular Atrophy, Postpoliomyelitis [description not available] | 0 | 3.79 | 2 | 1 |
Postpoliomyelitis Syndrome A syndrome characterized by new neuromuscular symptoms that occur at least 15 years after clinical stability has been attained in patients with a prior history of symptomatic poliomyelitis. Clinical features include new muscular weakness and atrophy of the limbs, bulbar innervated musculature, and muscles of respiration, combined with excessive fatigue, joint pain, and reduced stamina. The process is marked by slow progression and periods of stabilization. (From Ann NY Acad Sci 1995 May 25;753:68-80) | 0 | 3.79 | 2 | 1 |
Chronic Bronchitis [description not available] | 0 | 3.34 | 2 | 0 |
Chlamydia pneumoniae Infections [description not available] | 0 | 2.43 | 2 | 0 |
Bronchitis, Chronic A subcategory of CHRONIC OBSTRUCTIVE PULMONARY DISEASE. The disease is characterized by hypersecretion of mucus accompanied by a chronic (more than 3 months in 2 consecutive years) productive cough. Infectious agents are a major cause of chronic bronchitis. | 0 | 3.34 | 2 | 0 |
Acute Necrotizing Pancreatitis [description not available] | 0 | 3.41 | 1 | 1 |
Esophagitis, Reflux [description not available] | 0 | 3.33 | 2 | 0 |
Esophagitis, Peptic INFLAMMATION of the ESOPHAGUS that is caused by the reflux of GASTRIC JUICE with contents of the STOMACH and DUODENUM. | 0 | 3.33 | 2 | 0 |
Impairment, Light Touch Sensation [description not available] | 0 | 2.02 | 1 | 0 |
Kidney Stones [description not available] | 0 | 2.02 | 1 | 0 |
Choreoathetosis Self-Mutilation Hyperuricemia Syndrome [description not available] | 0 | 2.02 | 1 | 0 |
Autotomy Human [description not available] | 0 | 3.08 | 5 | 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 | 2.02 | 1 | 0 |
Lesch-Nyhan Syndrome An inherited disorder transmitted as a sex-linked trait and caused by a deficiency of an enzyme of purine metabolism; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE. Affected individuals are normal in the first year of life and then develop psychomotor retardation, extrapyramidal movement disorders, progressive spasticity, and seizures. Self-destructive behaviors such as biting of fingers and lips are seen frequently. Intellectual impairment may also occur but is typically not severe. Elevation of uric acid in the serum leads to the development of renal calculi and gouty arthritis. (Menkes, Textbook of Child Neurology, 5th ed, pp127) | 0 | 2.02 | 1 | 0 |
Bile Duct Obstruction, Intrahepatic [description not available] | 0 | 2.94 | 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 | 2.94 | 1 | 0 |
Aortic Stenosis [description not available] | 0 | 2.03 | 1 | 0 |
Aortitis Syndrome [description not available] | 0 | 2.38 | 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 | 2.03 | 1 | 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 | 2.38 | 2 | 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 | 2.44 | 2 | 0 |
Fasciitis Inflammation of the fascia. There are three major types: 1, Eosinophilic fasciitis, an inflammatory reaction with eosinophilia, producing hard thickened skin with an orange-peel configuration suggestive of scleroderma and considered by some a variant of scleroderma; 2, Necrotizing fasciitis (FASCIITIS, NECROTIZING), a serious fulminating infection (usually by a beta hemolytic streptococcus) causing extensive necrosis of superficial fascia; 3, Nodular/Pseudosarcomatous /Proliferative fasciitis, characterized by a rapid growth of fibroblasts with mononuclear inflammatory cells and proliferating capillaries in soft tissue, often the forearm; it is not malignant but is sometimes mistaken for fibrosarcoma. | 0 | 3.33 | 2 | 0 |
Epulides [description not available] | 0 | 2.03 | 1 | 0 |
Pericementitis [description not available] | 0 | 2.66 | 3 | 0 |
Gingival Diseases Diseases involving the GINGIVA. | 0 | 2.03 | 1 | 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 | 2.66 | 3 | 0 |
Crush Syndrome Severe systemic manifestation of trauma and ischemia involving soft tissues, principally skeletal muscle, due to prolonged severe crushing. It leads to increased permeability of the cell membrane and to the release of potassium, enzymes, and myoglobin from within cells. Ischemic renal dysfunction secondary to hypotension and diminished renal perfusion results in acute tubular necrosis and uremia. | 0 | 2.03 | 1 | 0 |
Cafe-au-Lait Spots Light brown pigmented macules associated with NEUROFIBROMATOSIS and Albright's syndrome (see FIBROUS DYSPLASIA, POLYOSTOTIC). | 0 | 2.94 | 1 | 0 |
Acropachy, Hereditary [description not available] | 0 | 2.41 | 2 | 0 |
Elephantiasis Neuromatosis [description not available] | 0 | 2.03 | 1 | 0 |
Neurofibroma, Plexiform A type of neurofibroma manifesting as a diffuse overgrowth of subcutaneous tissue, usually involving the face, scalp, neck, and chest but occasionally occurring in the abdomen or pelvis. The tumors tend to progress, and may extend along nerve roots to eventually involve the spinal roots and spinal cord. This process is almost always a manifestation of NEUROFIBROMATOSIS 1. (From Adams et al., Principles of Neurology, 6th ed, p1016; J Pediatr 1997 Nov;131(5):678-82) | 0 | 2.03 | 1 | 0 |
Benign Pilomatricoma [description not available] | 0 | 3.35 | 2 | 0 |
Abnormalities, Cardiovascular [description not available] | 0 | 2.03 | 1 | 0 |
Cardiovascular Abnormalities Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS. | 0 | 2.03 | 1 | 0 |
Colon Cancer, Familial Nonpolyposis [description not available] | 0 | 2.03 | 1 | 0 |
Colorectal Neoplasms, Hereditary Nonpolyposis A group of autosomal-dominant inherited diseases in which COLON CANCER arises in discrete adenomas. Unlike FAMILIAL POLYPOSIS COLI with hundreds of polyps, hereditary nonpolyposis colorectal neoplasms occur much later, in the fourth and fifth decades. HNPCC has been associated with germline mutations in mismatch repair (MMR) genes. It has been subdivided into Lynch syndrome I or site-specific colonic cancer, and LYNCH SYNDROME II which includes extracolonic cancer. | 0 | 2.03 | 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 | 2.03 | 1 | 0 |
Diabetes Mellitus, Gestational [description not available] | 0 | 3.34 | 2 | 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 | 3.34 | 2 | 0 |
Gammapathy, Monoclonal [description not available] | 0 | 2.03 | 1 | 0 |
Necrobiosis [description not available] | 0 | 3.32 | 2 | 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 | 2.03 | 1 | 0 |
Complications, Neoplastic Pregnancy [description not available] | 0 | 2.4 | 2 | 0 |
Abortion, Veterinary Premature expulsion of the FETUS in animals. | 0 | 3.46 | 8 | 0 |
Bronchiolitis, Exudative [description not available] | 0 | 2.95 | 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 | 2.95 | 1 | 0 |
Cot Death [description not available] | 0 | 4.76 | 12 | 0 |
Abdominal Cryptorchidism [description not available] | 0 | 3.34 | 7 | 0 |
Dermal Hypoplasia, Focal [description not available] | 0 | 2.03 | 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 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Injuries, Prenatal [description not available] | 0 | 2.03 | 1 | 0 |
Chromosomal Breakage [description not available] | 0 | 2.44 | 2 | 0 |
Alternating Exotropia [description not available] | 0 | 2.03 | 1 | 0 |
Allergic Cutaneous Angiitis [description not available] | 0 | 2.03 | 1 | 0 |
Acquired Laryngeal Stenosis [description not available] | 0 | 4.6 | 6 | 1 |
Haemophilus influenzae Meningitis Type B [description not available] | 0 | 2.67 | 3 | 0 |
Obesity Hypoventilation Syndrome HYPOVENTILATION syndrome in very obese persons with excessive ADIPOSE TISSUE around the ABDOMEN and DIAPHRAGM. It is characterized by diminished to absent ventilatory chemoresponsiveness; chronic HYPOXIA; HYPERCAPNIA; POLYCYTHEMIA; and long periods of sleep during day and night (HYPERSOMNOLENCE). It is a condition often related to OBSTRUCTIVE SLEEP APNEA but can occur separately. | 0 | 2.03 | 1 | 0 |
Aujeszky Disease [description not available] | 0 | 3.35 | 7 | 0 |
Angioleiomyoma [description not available] | 0 | 2.03 | 1 | 0 |
Blue Tongue [description not available] | 0 | 2.39 | 2 | 0 |
Obstructive Lung Diseases [description not available] | 0 | 12.87 | 47 | 9 |
Lung Diseases, Obstructive Any disorder marked by obstruction of conducting airways of the lung. AIRWAY OBSTRUCTION may be acute, chronic, intermittent, or persistent. | 0 | 12.87 | 47 | 9 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 2.03 | 1 | 0 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 2.03 | 1 | 0 |
Cerebrospinal Fluid Effusion, Subdural [description not available] | 0 | 2.03 | 1 | 0 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 2.66 | 3 | 0 |
Inflammation, Endodontic [description not available] | 0 | 2.03 | 1 | 0 |
Pulpitis Inflammation of the DENTAL PULP, usually due to bacterial infection in dental caries, tooth fracture, or other conditions causing exposure of the pulp to bacterial invasion. Chemical irritants, thermal factors, hyperemic changes, and other factors may also cause pulpitis. | 0 | 2.03 | 1 | 0 |
Anisometropia A condition of an inequality of refractive power of the two eyes. | 0 | 2.03 | 1 | 0 |
Osteosclerosis An abnormal hardening or increased density of bone tissue. | 0 | 3.62 | 3 | 0 |
Berger Disease [description not available] | 0 | 2.04 | 1 | 0 |
Glomerulonephritis, IGA A chronic form of glomerulonephritis characterized by deposits of predominantly IMMUNOGLOBULIN A in the mesangial area (GLOMERULAR MESANGIUM). Deposits of COMPLEMENT C3 and IMMUNOGLOBULIN G are also often found. Clinical features may progress from asymptomatic HEMATURIA to END-STAGE KIDNEY DISEASE. | 0 | 2.04 | 1 | 0 |
Hemiplegia, Crossed [description not available] | 0 | 3.04 | 5 | 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 | 3.04 | 5 | 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 | 3.75 | 11 | 0 |
Buphthalmos [description not available] | 0 | 1.93 | 1 | 0 |
Rida [description not available] | 0 | 2.04 | 1 | 0 |
California Encephalitis [description not available] | 0 | 2.04 | 1 | 0 |
HIV Lipodystrophy Syndrome [description not available] | 0 | 2.03 | 1 | 0 |
HIV-Associated Lipodystrophy Syndrome Defective metabolism leading to fat maldistribution in patients infected with HIV. The etiology appears to be multifactorial and probably involves some combination of infection-induced alterations in metabolism, direct effects of antiretroviral therapy, and patient-related factors. | 0 | 2.03 | 1 | 0 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 2.7 | 3 | 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 | 2.7 | 3 | 0 |
Cramp [description not available] | 0 | 2.35 | 2 | 0 |
Central Nervous System Origin Vertigo [description not available] | 0 | 2.36 | 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 | 2.35 | 2 | 0 |
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 | 2.36 | 2 | 0 |
Erythema Migrans, Lingual [description not available] | 0 | 3.55 | 3 | 0 |
Oral Manifestations Disorders of the mouth attendant upon non-oral disease or injury. | 0 | 3.96 | 5 | 0 |
Rheumatoid Nodule Subcutaneous nodules seen in 20-30% of rheumatoid arthritis patients. They may arise anywhere on the body, but are most frequently found over the bony prominences. The nodules are characterized histologically by dense areas of fibrinoid necrosis with basophilic streaks and granules, surrounded by a palisade of cells, mainly fibroblasts and histiocytes. | 0 | 2.37 | 2 | 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 | 2.35 | 2 | 0 |
Sex Disorders [description not available] | 0 | 1.96 | 1 | 0 |
Sexual Dysfunction, Physiological Physiological disturbances in normal sexual performance in either the male or the female. | 0 | 1.96 | 1 | 0 |
African Sleeping Sickness [description not available] | 0 | 1.96 | 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 | 1.96 | 1 | 0 |
Coronaviridae Infections Virus diseases caused by CORONAVIRIDAE. | 0 | 2.37 | 2 | 0 |
Infective Endocarditis [description not available] | 0 | 2.88 | 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 | 2.88 | 1 | 0 |
Labor, Premature [description not available] | 0 | 2.36 | 2 | 0 |
Infections, Legionella pneumophila [description not available] | 0 | 2.37 | 2 | 0 |
Endometrioma An enlarged area of ENDOMETRIOSIS that resembles a tumor. It is usually found in the OVARY. When it is filled with old blood, it is known as a chocolate cyst. | 0 | 1.96 | 1 | 0 |
Endometriosis A condition in which functional endometrial tissue is present outside the UTERUS. It is often confined to the PELVIS involving the OVARY, the ligaments, cul-de-sac, and the uterovesical peritoneum. | 0 | 1.96 | 1 | 0 |
Deficiency, Protein [description not available] | 0 | 2.36 | 2 | 0 |
Experimental Hepatoma [description not available] | 0 | 1.96 | 1 | 0 |
Leg Ulcer Ulceration of the skin and underlying structures of the lower extremity. About 90% of the cases are due to venous insufficiency (VARICOSE ULCER), 5% to arterial disease, and the remaining 5% to other causes. | 0 | 1.96 | 1 | 0 |
Bacteriuria The presence of bacteria in the urine which is normally bacteria-free. These bacteria are from the URINARY TRACT and are not contaminants of the surrounding tissues. Bacteriuria can be symptomatic or asymptomatic. Significant bacteriuria is an indicator of urinary tract infection. | 0 | 4.73 | 7 | 1 |
Deficiency, IgA [description not available] | 0 | 1.96 | 1 | 0 |
Deficiency, IgG [description not available] | 0 | 1.96 | 1 | 0 |
Dysgammaglobulinemia An immunologic deficiency state characterized by selective deficiencies of one or more, but not all, classes of immunoglobulins. | 0 | 1.96 | 1 | 0 |
Duodenal Obstruction Hindrance of the passage of luminal contents in the DUODENUM. Duodenal obstruction can be partial or complete, and caused by intrinsic or extrinsic factors. Simple obstruction is associated with diminished or stopped flow of luminal contents. Strangulating obstruction is associated with impaired blood flow to the duodenum in addition to obstructed flow of luminal contents. | 0 | 1.96 | 1 | 0 |
Chronic Idiopathic Intestinal Pseudo-Obstruction [description not available] | 0 | 1.96 | 1 | 0 |
Intestinal Pseudo-Obstruction A type of ILEUS, a functional not mechanical obstruction of the INTESTINES. This syndrome is caused by a large number of disorders involving the smooth muscles (MUSCLE, SMOOTH) or the NERVOUS SYSTEM. | 0 | 1.96 | 1 | 0 |
Arthritis, Juvenile Chronic [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Epiglottitis Inflammation of the EPIGLOTTIS. | 0 | 2.66 | 3 | 0 |
Spherocytosis, Hereditary A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions. | 0 | 1.96 | 1 | 0 |
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 | 1.96 | 1 | 0 |
Amyoplasia Congenita [description not available] | 0 | 2.36 | 2 | 0 |
Dermatosclerosis [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Developmental Psychomotor Disorders [description not available] | 0 | 4.44 | 5 | 0 |
Bessel-Hagen Disease [description not available] | 0 | 3.21 | 6 | 0 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 1.96 | 1 | 0 |
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 | 1.96 | 1 | 0 |
Cerebral Arteriosclerosis [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Abnormalities, Sex Chromosome [description not available] | 0 | 2.36 | 2 | 0 |
Colitis Gravis [description not available] | 0 | 2.89 | 4 | 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 | 2.89 | 4 | 0 |
Abortion, Tubal [description not available] | 0 | 2.35 | 2 | 0 |
Abortion, Spontaneous Expulsion of the product of FERTILIZATION before completing the term of GESTATION and without deliberate interference. | 0 | 2.35 | 2 | 0 |
Hypoproteinemia A condition in which total serum protein level is below the normal range. Hypoproteinemia can be caused by protein malabsorption in the gastrointestinal tract, EDEMA, or PROTEINURIA. | 0 | 1.96 | 1 | 0 |
Osteolysis Dissolution of bone that particularly involves the removal or loss of calcium. | 0 | 1.96 | 1 | 0 |
Hematuria Presence of blood in the urine. | 0 | 1.95 | 1 | 0 |
Cor Pulmonale [description not available] | 0 | 1.95 | 1 | 0 |
Pigmentary Retinopathy [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Complications, Hematologic Pregnancy [description not available] | 0 | 2.65 | 3 | 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 | 4.29 | 1 | 1 |
Infections, Neisseriaceae [description not available] | 0 | 1.98 | 1 | 0 |
Adenomatous Polyps Benign neoplasms derived from glandular epithelium. (From Stedman, 25th ed) | 0 | 1.98 | 1 | 0 |
Hypocapnia Clinical manifestation consisting of a deficiency of carbon dioxide in arterial blood. | 0 | 1.98 | 1 | 0 |
Dermatitis, Radiation-Induced [description not available] | 0 | 3.58 | 3 | 0 |
Radiodermatitis A cutaneous inflammatory reaction occurring as a result of exposure to ionizing radiation. | 0 | 3.58 | 3 | 0 |
Hepatic Porphyria [description not available] | 0 | 1.98 | 1 | 0 |
Porphyrias, Hepatic A group of metabolic diseases due to deficiency of one of a number of LIVER enzymes in the biosynthetic pathway of HEME. They are characterized by the accumulation and increased excretion of PORPHYRINS or its precursors. Clinical features include neurological symptoms (PORPHYRIA, ACUTE INTERMITTENT), cutaneous lesions due to photosensitivity (PORPHYRIA CUTANEA TARDA), or both (HEREDITARY COPROPORPHYRIA). Hepatic porphyrias can be hereditary or acquired as a result of toxicity to the hepatic tissues. | 0 | 1.98 | 1 | 0 |
Endomyometritis Inflammation of both the ENDOMETRIUM and the MYOMETRIUM, usually caused by infections after a CESAREAN SECTION. | 0 | 1.98 | 1 | 0 |
Endometritis Inflammation of the ENDOMETRIUM, usually caused by intrauterine infections. Endometritis is the most common cause of postpartum fever. | 0 | 1.98 | 1 | 0 |
Cretinism [description not available] | 0 | 3.56 | 3 | 0 |
Congenital Hypothyroidism A condition in infancy or early childhood due to an in-utero deficiency of THYROID HORMONES that can be caused by genetic or environmental factors, such as thyroid dysgenesis or HYPOTHYROIDISM in infants of mothers treated with THIOURACIL during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe MENTAL RETARDATION, impaired skeletal development, short stature, and MYXEDEMA. | 0 | 3.56 | 3 | 0 |
A-V Dissociation [description not available] | 0 | 2.66 | 3 | 0 |
Polycystic Ovarian Syndrome [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Autonomic Failure, Progressive [description not available] | 0 | 1.98 | 1 | 0 |
Adipocere [description not available] | 0 | 2.88 | 4 | 0 |
Femoral Fractures Fractures of the femur. | 0 | 3.78 | 4 | 0 |
Athlete's Foot [description not available] | 0 | 1.98 | 1 | 0 |
Tinea Pedis Dermatological pruritic lesion in the feet, caused by Trichophyton rubrum, T. mentagrophytes, or Epidermophyton floccosum. | 0 | 1.98 | 1 | 0 |
Histiocytic Sarcoma Malignant neoplasms composed of MACROPHAGES or DENDRITIC CELLS. Most histiocytic sarcomas present as localized tumor masses without a leukemic phase. Though the biological behavior of these neoplasms resemble lymphomas, their cell lineage is histiocytic not lymphoid. | 0 | 1.98 | 1 | 0 |
Miliaria A syndrome of cutaneous changes associated with sweat retention and extravasation of sweat at different levels in the skin. Miliaria rubra, or prickly heat, results from apocrine duct obstruction. The sweat then seeps into the epidermis, producing pruritic erythematous papulovesicles. (From Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Ureteral Obstruction Blockage in any part of the URETER causing obstruction of urine flow from the kidney to the URINARY BLADDER. The obstruction may be congenital, acquired, unilateral, bilateral, complete, partial, acute, or chronic. Depending on the degree and duration of the obstruction, clinical features vary greatly such as HYDRONEPHROSIS and obstructive nephropathy. | 0 | 3.31 | 2 | 0 |
Ghost Teeth [description not available] | 0 | 2.39 | 2 | 0 |
Achalasia [description not available] | 0 | 2.66 | 3 | 0 |
Cold Fingers, Hereditary [description not available] | 0 | 3.79 | 4 | 0 |
Sclerosis, Systemic [description not available] | 0 | 1.98 | 1 | 0 |
Esophageal Achalasia A motility disorder of the ESOPHAGUS in which the LOWER ESOPHAGEAL SPHINCTER (near the CARDIA) fails to relax resulting in functional obstruction of the esophagus, and DYSPHAGIA. Achalasia is characterized by a grossly contorted and dilated esophagus (megaesophagus). | 0 | 2.66 | 3 | 0 |
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 | 3.79 | 4 | 0 |
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 | 1.98 | 1 | 0 |
HbS Disease [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 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 | 3.65 | 10 | 0 |
Chromosomes, Ring [description not available] | 0 | 1.98 | 1 | 0 |
Aneurysm, Bacterial [description not available] | 0 | 1.98 | 1 | 0 |
Antibody Deficiency Syndrome [description not available] | 0 | 3.99 | 5 | 0 |
Infections, Mycobacterium [description not available] | 0 | 1.98 | 1 | 0 |
Immunologic Deficiency Syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. | 0 | 3.99 | 5 | 0 |
Mycobacterium Infections Infections with bacteria of the genus MYCOBACTERIUM. | 0 | 1.98 | 1 | 0 |
Acid beta-Glucosidase Deficiency [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 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 | 2.38 | 2 | 0 |
Clubfeet [description not available] | 0 | 3.21 | 6 | 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 | 4.26 | 7 | 0 |
Varices [description not available] | 0 | 1.98 | 1 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 1.98 | 1 | 0 |
(pPNET) Peripheral Primitive Neuroectodermal Tumors [description not available] | 0 | 3.97 | 14 | 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 | 3.97 | 14 | 0 |
Inadequate Sleep [description not available] | 0 | 2.36 | 2 | 0 |
Prediabetes [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Drowning Death that occurs as a result of anoxia or heart arrest, associated with immersion in liquid. | 0 | 1.98 | 1 | 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 | 2.9 | 1 | 0 |
Follicular Thyroid Carcinoma [description not available] | 0 | 1.98 | 1 | 0 |
Adenocarcinoma, Follicular An adenocarcinoma of the thyroid gland, in which the cells are arranged in the form of follicles. (From Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Cushing's Syndrome [description not available] | 0 | 1.99 | 1 | 0 |
Adenoma, Chromophobe A benign tumor of the anterior pituitary in which the cells do not stain with acidic or basic dyes. | 0 | 2.38 | 2 | 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 | 1.99 | 1 | 0 |
Cancer of Colon [description not available] | 0 | 4.25 | 4 | 0 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 4.25 | 4 | 0 |
Right Ventricular Dysfunction [description not available] | 0 | 1.99 | 1 | 0 |
Cow Pox [description not available] | 0 | 1.99 | 1 | 0 |
Lung Diseases, Parasitic Infections of the lungs with parasites, most commonly by parasitic worms (HELMINTHS). | 0 | 3.37 | 1 | 1 |
Amniotic Fluid Embolism [description not available] | 0 | 2.37 | 2 | 0 |
Stomatitis, Denture Inflammation of the mouth due to denture irritation. | 0 | 1.99 | 1 | 0 |
AIDS Seroconversion [description not available] | 0 | 3.31 | 2 | 0 |
Infections, Microspora [description not available] | 0 | 3.31 | 2 | 0 |
Dermatitis Seborrheica [description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Exertional Heat Illness [description not available] | 0 | 2.91 | 1 | 0 |
Injuries, Knee [description not available] | 0 | 3.3 | 2 | 0 |
Sprains [description not available] | 0 | 2.91 | 1 | 0 |
Ankle Injuries Harm or hurt to the ankle or ankle joint usually inflicted by an external source. | 0 | 3.77 | 2 | 0 |
Knee Injuries Injuries to the knee or the knee joint. | 0 | 3.3 | 2 | 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 | 2.91 | 1 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 1.99 | 1 | 0 |
Fallot's Tetralogy [description not available] | 0 | 2.65 | 3 | 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 | 2.65 | 3 | 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 | 2.66 | 3 | 0 |
Auto-PEEP [description not available] | 0 | 4.35 | 2 | 2 |
Hearing Loss, High-Frequency Hearing loss in frequencies above 1000 hertz. | 0 | 1.99 | 1 | 0 |
Hyperkeratosis Palmaris et Plantaris [description not available] | 0 | 1.99 | 1 | 0 |
Chromosome-Defective Micronuclei [description not available] | 0 | 1.99 | 1 | 0 |
Farsightedness [description not available] | 0 | 1.99 | 1 | 0 |
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 | 1.99 | 1 | 0 |
Lipomatosis A disorder characterized by the accumulation of encapsulated or unencapsulated tumor-like fatty tissue resembling LIPOMA. | 0 | 2.91 | 1 | 0 |
Foot Deformities Alterations or deviations from normal shape or size which result in a disfigurement of the foot. | 0 | 2.91 | 1 | 0 |
Absence of Voice [description not available] | 0 | 1.99 | 1 | 0 |
Infant, Small for Gestational Age An infant having a birth weight lower than expected for its gestational age. | 0 | 3.76 | 2 | 1 |
Cryptosporidium Infection [description not available] | 0 | 2.91 | 1 | 0 |
Histomoniasis [description not available] | 0 | 2.91 | 1 | 0 |
Cryptosporidiosis Intestinal infection with organisms of the genus CRYPTOSPORIDIUM. It occurs in both animals and humans. Symptoms include severe DIARRHEA. | 0 | 2.91 | 1 | 0 |
Bacterial Vaginitides [description not available] | 0 | 1.99 | 1 | 0 |
Vaginosis, Bacterial Polymicrobial, nonspecific vaginitis associated with positive cultures of Gardnerella vaginalis and other anaerobic organisms and a decrease in lactobacilli. It remains unclear whether the initial pathogenic event is caused by the growth of anaerobes or a primary decrease in lactobacilli. | 0 | 1.99 | 1 | 0 |
Leg Dermatoses A nonspecific term used to denote any cutaneous lesion or group of lesions, or eruptions of any type on the leg. (From Stedman, 25th ed) | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
African Lymphoma [description not available] | 0 | 1.99 | 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 | 1.99 | 1 | 0 |
Congenital Tracheobronchomegaly [description not available] | 0 | 2.91 | 1 | 0 |
Infections, Chlamydia [description not available] | 0 | 1.99 | 1 | 0 |
Chlamydia Infections Infections with bacteria of the genus CHLAMYDIA. | 0 | 1.99 | 1 | 0 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 1.99 | 1 | 0 |
Cerebromalacia [description not available] | 0 | 1.99 | 1 | 0 |
Periapical Cyst [description not available] | 0 | 2.37 | 2 | 0 |
Pleuropneumonia Inflammation of the lung parenchyma that is associated with PLEURISY, inflammation of the PLEURA. | 0 | 2.37 | 2 | 0 |
Anemia, Hypoplastic [description not available] | 0 | 2.37 | 2 | 0 |
Anemia, Aplastic A form of anemia in which the bone marrow fails to produce adequate numbers of peripheral blood elements. | 0 | 2.37 | 2 | 0 |
Atresia, Pulmonary [description not available] | 0 | 2.91 | 1 | 0 |
Bladder Exstrophy A birth defect in which the URINARY BLADDER is malformed and exposed, inside out, and protruded through the ABDOMINAL WALL. It is caused by closure defects involving the top front surface of the bladder, as well as the lower abdominal wall; SKIN; MUSCLES; and the pubic bone. | 0 | 2.91 | 1 | 0 |
Abnormalities, Radiation-Induced Congenital changes in the morphology of organs produced by exposure to ionizing or non-ionizing radiation. | 0 | 1.99 | 1 | 0 |
Vulvar Diseases Pathological processes of the VULVA. | 0 | 2.91 | 1 | 0 |
Viral Conjunctivitis [description not available] | 0 | 2.4 | 2 | 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 | 2.4 | 2 | 0 |
Jaw Diseases Diseases involving the JAW. | 0 | 3.58 | 3 | 0 |
Fibro-Odontoma [description not available] | 0 | 3.32 | 2 | 0 |
Calciphylaxes [description not available] | 0 | 1.99 | 1 | 0 |
Penile Diseases Pathological processes involving the PENIS or its component tissues. | 0 | 1.99 | 1 | 0 |
Aerophagy Spasmodic swallowing of air. | 0 | 2.37 | 2 | 0 |
Adenitis, Salivary Gland [description not available] | 0 | 1.99 | 1 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 3.77 | 2 | 1 |
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 | 3.77 | 2 | 1 |
Fibrous Dysplasia, Monostotic FIBROUS DYSPLASIA OF BONE involving only one bone. | 0 | 3.3 | 2 | 0 |
Gingival Hyperplasia Non-inflammatory enlargement of the gingivae produced by factors other than local irritation. It is characteristically due to an increase in the number of cells. (From Jablonski's Dictionary of Dentistry, 1992, p400) | 0 | 3.29 | 2 | 0 |
Laryngeal Spasm [description not available] | 0 | 4.27 | 4 | 1 |
Laryngismus A disorder in which the adductor muscles of the VOCAL CORDS exhibit increased activity leading to laryngeal spasm. Laryngismus causes closure of the VOCAL FOLDS and airflow obstruction during inspiration. | 0 | 4.27 | 4 | 1 |
Attrition, Dental [description not available] | 0 | 2 | 1 | 0 |
Bruxism A disorder characterized by grinding and clenching of the teeth. | 0 | 2.37 | 2 | 0 |
Erosive Duodenitis [description not available] | 0 | 2 | 1 | 0 |
Duodenitis Inflammation of the DUODENUM section of the small intestine (INTESTINE, SMALL). Erosive duodenitis may cause bleeding in the UPPER GI TRACT and PEPTIC ULCER. | 0 | 2 | 1 | 0 |
Auricular Fibrillation [description not available] | 0 | 3.38 | 1 | 1 |
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 | 3.38 | 1 | 1 |
Cancer of Testis [description not available] | 0 | 2.4 | 2 | 0 |
Choriocarcinoma A malignant metastatic form of trophoblastic tumors. Unlike the HYDATIDIFORM MOLE, choriocarcinoma contains no CHORIONIC VILLI but rather sheets of undifferentiated cytotrophoblasts and syncytiotrophoblasts (TROPHOBLASTS). It is characterized by the large amounts of CHORIONIC GONADOTROPIN produced. Tissue origins can be determined by DNA analyses: placental (fetal) origin or non-placental origin (CHORIOCARCINOMA, NON-GESTATIONAL). | 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 | 2.4 | 2 | 0 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 2.37 | 2 | 0 |
Hyponatremia Deficiency of sodium in the blood; salt depletion. (Dorland, 27th ed) | 0 | 2 | 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 | 2.37 | 2 | 0 |
Nutritional Disorders [description not available] | 0 | 2.38 | 2 | 0 |
Gastric Dilatation Abnormal distention of the STOMACH due to accumulation of gastric contents that may reach 10 to 15 liters. Gastric dilatation may be the result of GASTRIC OUTLET OBSTRUCTION; ILEUS; GASTROPARESIS; or denervation. | 0 | 2 | 1 | 0 |
Battered Child Syndrome A clinical condition resulting from repeated physical and psychological injuries inflicted on a child by the parents or caregivers. | 0 | 2 | 1 | 0 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 2.38 | 2 | 0 |
Age-Related Macular Degeneration [description not available] | 0 | 2 | 1 | 0 |
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 | 2 | 1 | 0 |
Cranial Epidural Hematoma [description not available] | 0 | 2 | 1 | 0 |
Bernard-Soulier Syndrome A familial coagulation disorder characterized by a prolonged bleeding time, unusually large platelets, and impaired prothrombin consumption. | 0 | 2 | 1 | 0 |
Anterior Horn Cell Disease [description not available] | 0 | 3.79 | 2 | 1 |
Motor Neuron Disease Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy (BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 3.79 | 2 | 1 |
Premature Rupture of Fetal Membranes [description not available] | 0 | 2 | 1 | 0 |
Fetal Membranes, Premature Rupture Spontaneous tearing of the membranes surrounding the FETUS any time before the onset of OBSTETRIC LABOR. Preterm PROM is membrane rupture before 37 weeks of GESTATION. | 0 | 2 | 1 | 0 |
Coxsackie Virus Infections [description not available] | 0 | 4.04 | 3 | 1 |
Bulbar Palsy [description not available] | 0 | 2.37 | 2 | 0 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 2.65 | 3 | 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 | 2.65 | 3 | 0 |
Carcinoma, Large Cell A tumor of undifferentiated (anaplastic) cells of large size. It is usually bronchogenic. (From Dorland, 27th ed) | 0 | 2.92 | 1 | 0 |
Germinoma A malignant neoplasm of the germinal tissue of the GONADS; MEDIASTINUM; or pineal region. Germinomas are uniform in appearance, consisting of large, round cells with vesicular nuclei and clear or finely granular eosinophilic-staining cytoplasm. (Stedman, 265th ed; from DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, pp1642-3) | 0 | 2.92 | 1 | 0 |
Atelectasis [description not available] | 0 | 4.26 | 4 | 1 |
Edema, Pulmonary [description not available] | 0 | 4.59 | 6 | 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 | 4.59 | 6 | 0 |
Adult Premature Aging Syndrome [description not available] | 0 | 2.37 | 2 | 0 |
Cancer of Muscle [description not available] | 0 | 2 | 1 | 0 |
Balanitis Inflammation of the head of the PENIS, glans penis. | 0 | 2 | 1 | 0 |
Dizzyness [description not available] | 0 | 2 | 1 | 0 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 2 | 1 | 0 |
Atrioventricular Nodal Re-Entrant Tachycardia [description not available] | 0 | 2 | 1 | 0 |
Tachycardia, Ventricular An abnormally rapid ventricular rhythm usually in excess of 150 beats per minute. It is generated within the ventricle below the BUNDLE OF HIS, either as autonomic impulse formation or reentrant impulse conduction. Depending on the etiology, onset of ventricular tachycardia can be paroxysmal (sudden) or nonparoxysmal, its wide QRS complexes can be uniform or polymorphic, and the ventricular beating may be independent of the atrial beating (AV dissociation). | 0 | 2 | 1 | 0 |
Thrombocythemia [description not available] | 0 | 2 | 1 | 0 |
Deficiency, Vitamin K [description not available] | 0 | 3.3 | 2 | 0 |
Vitamin K Deficiency A nutritional condition produced by a deficiency of VITAMIN K in the diet, characterized by an increased tendency to hemorrhage (HEMORRHAGIC DISORDERS). Such bleeding episodes may be particularly severe in newborn infants. (From Cecil Textbook of Medicine, 19th ed, p1182) | 0 | 3.3 | 2 | 0 |
Aortic Arch Syndrome [description not available] | 0 | 2.38 | 2 | 0 |
Oligohydramnios A condition of abnormally low AMNIOTIC FLUID volume. Principal causes include malformations of fetal URINARY TRACT; FETAL GROWTH RETARDATION; GESTATIONAL HYPERTENSION; nicotine poisoning; and PROLONGED PREGNANCY. | 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 |
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 | 2 | 1 | 0 |
Tooth Drift [description not available] | 0 | 2 | 1 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 2 | 1 | 0 |
Angiofollicular Lymph Hyperplasia [description not available] | 0 | 2 | 1 | 0 |
Castleman Disease Large benign, hyperplastic lymph nodes. The more common hyaline vascular subtype is characterized by small hyaline vascular follicles and interfollicular capillary proliferations. Plasma cells are often present and represent another subtype with the plasma cells containing IgM and IMMUNOGLOBULIN A. | 0 | 2 | 1 | 0 |
Acute Kidney Failure [description not available] | 0 | 2 | 1 | 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 | 2 | 1 | 0 |
Aging, Premature Changes in the organism associated with senescence, occurring at an accelerated rate. | 0 | 2 | 1 | 0 |
Exostoses Benign hypertrophy that projects outward from the surface of bone, often containing a cartilaginous component. | 0 | 2.39 | 2 | 0 |
Periapical Diseases Diseases of the PERIAPICAL TISSUE surrounding the root of the tooth, which is distinguished from DENTAL PULP DISEASES inside the TOOTH ROOT. | 0 | 2.38 | 2 | 0 |
Dental Granuloma [description not available] | 0 | 2.36 | 2 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 2 | 1 | 0 |
Cyst, Pulmonary Hydatid [description not available] | 0 | 2 | 1 | 0 |
Biliary Fistula Abnormal passage in any organ of the biliary tract or between biliary organs and other organs. | 0 | 2.39 | 2 | 0 |
Alveolar Echinococcosis, Hepatic [description not available] | 0 | 2.39 | 2 | 0 |
Bronchial Fistula An abnormal passage or communication between a bronchus and another part of the body. | 0 | 2 | 1 | 0 |
Sinus Pericranii Rare vascular anomaly involving a communication between the intracranial and extracranial venous circulation via diploe, the central spongy layer of cranial bone. It is often characterized by dilated venous structures on the scalp due to abnormal drainage from the intracranial venous sinuses. Sinus pericranii can be congenital or traumatic in origin. | 0 | 2.92 | 1 | 0 |
Arterivirus Infections Infections caused by viruses of the genus ARTERIVIRUS. | 0 | 2 | 1 | 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 | 2 | 1 | 0 |
Infections, Rhabdoviridae [description not available] | 0 | 2.01 | 1 | 0 |
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans [description not available] | 0 | 2.37 | 2 | 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 | 2.37 | 2 | 0 |
Dentin Dysplasia An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed) | 0 | 2.01 | 1 | 0 |
BH4 Deficiency [description not available] | 0 | 2.64 | 3 | 0 |
Phenylketonurias A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952). | 0 | 2.64 | 3 | 0 |
Autokinetic Effect [description not available] | 0 | 2.38 | 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 | 3.33 | 1 | 1 |
Gelineau Syndrome [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Gastric Fistula Abnormal passage communicating with the STOMACH. | 0 | 1.95 | 1 | 0 |
Pancreatic Fistula Abnormal passage communicating with the PANCREAS. | 0 | 1.95 | 1 | 0 |
Agranulocytosis A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS). | 0 | 2.87 | 4 | 0 |
Convulsions, Grand Mal [description not available] | 0 | 3.27 | 2 | 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 | 3.27 | 2 | 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 | 1.95 | 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 | 2.64 | 3 | 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 | 2.64 | 3 | 0 |
Plica Syndrome [description not available] | 0 | 2.64 | 3 | 0 |
Synovitis Inflammation of the SYNOVIAL MEMBRANE. | 0 | 2.64 | 3 | 0 |
Gastroenteritis, Transmissible, of Swine A condition of chronic gastroenteritis in adult pigs and fatal gastroenteritis in piglets caused by a CORONAVIRUS. | 0 | 2.35 | 2 | 0 |
Vulvovaginitis Inflammation of the VULVA and the VAGINA, characterized by discharge, burning, and PRURITUS. | 0 | 1.95 | 1 | 0 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 2.66 | 3 | 0 |
Encephalomyelitis, Enzootic Porcine A picornavirus infection producing symptoms similar to poliomyelitis in pigs. | 0 | 2.35 | 2 | 0 |
Swine Vesicular Disease An enterovirus infection of swine clinically indistinguishable from FOOT-AND-MOUTH DISEASE, vesicular stomatitis, and VESICULAR EXANTHEMA OF SWINE. It is caused by a strain of HUMAN ENTEROVIRUS B. | 0 | 1.95 | 1 | 0 |
Aseptic Necrosis of Femur Head [description not available] | 0 | 2.36 | 2 | 0 |
Branchial Cleft Cyst [description not available] | 0 | 1.95 | 1 | 0 |
Periodontitis, Acute Nonsuppurative [description not available] | 0 | 1.95 | 1 | 0 |
Periapical Periodontitis Inflammation of the PERIAPICAL TISSUE. It includes general, unspecified, or acute nonsuppurative inflammation. Chronic nonsuppurative inflammation is PERIAPICAL GRANULOMA. Suppurative inflammation is PERIAPICAL ABSCESS. | 0 | 1.95 | 1 | 0 |
Dysplasia Linguofacialis [description not available] | 0 | 3.78 | 4 | 0 |
Aneurysm, Aortic [description not available] | 0 | 1.95 | 1 | 0 |
Aortic Aneurysm, Ruptured [description not available] | 0 | 1.95 | 1 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 1.95 | 1 | 0 |
Dextro-Looped Transposition of the Great Arteries [description not available] | 0 | 1.95 | 1 | 0 |
Transposition of Great Vessels A congenital cardiovascular malformation in which the AORTA arises entirely from the RIGHT VENTRICLE, and the PULMONARY ARTERY arises from the LEFT VENTRICLE. Consequently, the pulmonary and the systemic circulations are parallel and not sequential, so that the venous return from the peripheral circulation is re-circulated by the right ventricle via aorta to the systemic circulation without being oxygenated in the lungs. This is a potentially lethal form of heart disease in newborns and infants. | 0 | 1.95 | 1 | 0 |
Malabsorption Syndromes General term for a group of MALNUTRITION syndromes caused by failure of normal INTESTINAL ABSORPTION of nutrients. | 0 | 3.2 | 6 | 0 |
Antibiotic-Associated Colitis [description not available] | 0 | 2.64 | 3 | 0 |
Enterocolitis, Pseudomembranous An acute inflammation of the INTESTINAL MUCOSA that is characterized by the presence of pseudomembranes or plaques in the SMALL INTESTINE (pseudomembranous enteritis) and the LARGE INTESTINE (pseudomembranous colitis). It is commonly associated with antibiotic therapy and CLOSTRIDIUM DIFFICILE colonization. | 0 | 2.64 | 3 | 0 |
Creeping Eruption [description not available] | 0 | 1.95 | 1 | 0 |
Salivary Gland Diseases Diseases involving the SALIVARY GLANDS. | 0 | 2.87 | 4 | 0 |
Intestinal Perforation Opening or penetration through the wall of the INTESTINES. | 0 | 2.64 | 3 | 0 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 2.35 | 2 | 0 |
Adenitis [description not available] | 0 | 3.45 | 8 | 0 |
Bacterial Endocarditides, Subacute [description not available] | 0 | 1.95 | 1 | 0 |
Spondylisthesis [description not available] | 0 | 1.95 | 1 | 0 |
Negativistic Personality Disorder [description not available] | 0 | 1.95 | 1 | 0 |
Clubbed Fingers [description not available] | 0 | 1.95 | 1 | 0 |
Intussusception A form of intestinal obstruction caused by the PROLAPSE of a part of the intestine into the adjoining intestinal lumen. There are four types: colic, involving segments of the LARGE INTESTINE; enteric, involving only the SMALL INTESTINE; ileocecal, in which the ILEOCECAL VALVE prolapses into the CECUM, drawing the ILEUM along with it; and ileocolic, in which the ileum prolapses through the ileocecal valve into the COLON. | 0 | 1.95 | 1 | 0 |
Marasmus [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Deficiency, Glucosephosphatase [description not available] | 0 | 1.95 | 1 | 0 |
Glycogen Storage Disease Type I An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood. | 0 | 1.95 | 1 | 0 |
Infantile Diarrhea [description not available] | 0 | 2.64 | 3 | 0 |
Diarrhea, Infantile DIARRHEA occurring in infants from newborn to 24-months old. | 0 | 2.64 | 3 | 0 |
Protozoan Infections, Animal Infections with unicellular organisms formerly members of the subkingdom Protozoa. The infections may be experimental or veterinary. | 0 | 1.95 | 1 | 0 |
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 | 1.95 | 1 | 0 |
Coronary Heart Disease [description not available] | 0 | 2.36 | 2 | 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 | 2.36 | 2 | 0 |
Echo Virus Infections [description not available] | 0 | 2.64 | 3 | 0 |
Cancer of Prostate [description not available] | 0 | 2.35 | 2 | 0 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 2.35 | 2 | 0 |
Blastomyces brasiliensis Infection [description not available] | 0 | 1.95 | 1 | 0 |
Cancer of Penis [description not available] | 0 | 1.95 | 1 | 0 |
Penile Neoplasms Cancers or tumors of the PENIS or of its component tissues. | 0 | 1.95 | 1 | 0 |
Diffuse Myofascial Pain Syndrome [description not available] | 0 | 1.95 | 1 | 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 | 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 | 3.74 | 2 | 1 |
Corneal Diseases Diseases of the cornea. | 0 | 3.28 | 2 | 0 |
Convalescence The period of recovery following an illness. | 0 | 3.75 | 2 | 1 |
Arterial Diseases, Cerebral [description not available] | 0 | 1.95 | 1 | 0 |
Cerebral Arterial Diseases Pathological conditions of intracranial ARTERIES supplying the CEREBRUM. These diseases often are due to abnormalities or pathological processes in the ANTERIOR CEREBRAL ARTERY; MIDDLE CEREBRAL ARTERY; and POSTERIOR CEREBRAL ARTERY. | 0 | 1.95 | 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 | 2.35 | 2 | 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 | 1.95 | 1 | 0 |
Elaeophoriasis [description not available] | 0 | 2.35 | 2 | 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 | 2.35 | 2 | 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 | 2.36 | 2 | 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 | 1.95 | 1 | 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 | 2.35 | 2 | 0 |
Rib Fractures Fractures of any of the RIBS. | 0 | 2.64 | 3 | 0 |
Hepatitis, Viral, Animal INFLAMMATION of the LIVER in animals due to viral infection. | 0 | 2.89 | 4 | 0 |
Infections, Salmonella [description not available] | 0 | 1.98 | 1 | 0 |
Food Poisoning [description not available] | 0 | 2.36 | 2 | 0 |
Deficiency, Ascorbic Acid [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Jaw, Edentulous, Partially Absence of teeth from a portion of the mandible and/or maxilla. | 0 | 1.98 | 1 | 0 |
Periphlebitis Periphlebitis is inflammation of the outer coat of a vein or of tissues surrounding the vein. | 0 | 2.38 | 2 | 0 |
Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). | 0 | 2.38 | 2 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 1.98 | 1 | 0 |
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 | 1.98 | 1 | 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 | 2.89 | 1 | 0 |
Addison's Anemia [description not available] | 0 | 2.38 | 2 | 0 |
Cocarcinogenesis The combination of two or more different factors in the production of cancer. | 0 | 1.98 | 1 | 0 |
Dermatitis Exfoliativa [description not available] | 0 | 1.98 | 1 | 0 |
Dermatitis, Exfoliative The widespread involvement of the skin by a scaly, erythematous dermatitis occurring either as a secondary or reactive process to an underlying cutaneous disorder (e.g., atopic dermatitis, psoriasis, etc.), or as a primary or idiopathic disease. It is often associated with the loss of hair and nails, hyperkeratosis of the palms and soles, and pruritus. (From Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Poisoning, Lead [description not available] | 0 | 1.98 | 1 | 0 |
Lead Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of LEAD or lead compounds. | 0 | 1.98 | 1 | 0 |
Absent Iris [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Childhood Torsion Disease [description not available] | 0 | 1.98 | 1 | 0 |
Hypermyotonia [description not available] | 0 | 1.97 | 1 | 0 |
Hypercementosis A regressive change of teeth characterized by excessive development of secondary cementum on the tooth surface. It may occur on any part of the root, but the apical two-thirds are most commonly affected. (Dorland, 27th ed) | 0 | 1.97 | 1 | 0 |
Chromoblastomycosis Scaly papule or warty growth, caused by five fungi, that spreads as a result of satellite lesions affecting the foot or leg. The extremity may become swollen and, at its distal portion, covered with various nodular, tumorous, verrucous lesions that resemble cauliflower. In rare instances, the disease may begin on the hand or wrist and involve the entire upper extremity. (Arnold, Odom, and James, Andrew's Diseases of the Skin, 8th ed, p362) | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Teeth, Unerupted [description not available] | 0 | 1.97 | 1 | 0 |
Bacterial Conjunctivitides [description not available] | 0 | 2.38 | 2 | 0 |
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 | 2.38 | 2 | 0 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 2.89 | 1 | 0 |
B. burgdorferi Infection [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 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 | 1.97 | 1 | 0 |
Labhart-Willi Syndrome [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Infectious Endophthalmitis Infectious condition of the internal eye. | 0 | 6.26 | 9 | 0 |
Endophthalmitis Suppurative inflammation of the tissues of the internal structures of the eye frequently associated with an infection. | 0 | 6.26 | 9 | 0 |
Brock's Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Glaucoma, Angle Closure [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Anguilluliasis [description not available] | 0 | 1.97 | 1 | 0 |
Strongyloidiasis Infection with nematodes of the genus STRONGYLOIDES. The presence of larvae may produce pneumonitis and the presence of adult worms in the intestine could lead to moderate to severe diarrhea. | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Dwarfism, Thanatophoric [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Toxemia A condition produced by the presence of toxins or other harmful substances in the BLOOD. | 0 | 3.36 | 1 | 1 |
Apudoma A general term collectively applied to tumors associated with the APUD CELLS series, irrespective of their specific identification. | 0 | 1.97 | 1 | 0 |
Common Bile Duct Diseases Diseases of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | 0 | 2.37 | 2 | 0 |
Chicken Pox [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Adenoma, Acidophil A benign tumor, usually found in the anterior lobe of the pituitary gland, whose cells stain with acid dyes. Such pituitary tumors may give rise to excessive secretion of growth hormone, resulting in gigantism or acromegaly. A specific type of acidophil adenoma may give rise to nonpuerperal galactorrhea. (Dorland, 27th ed) | 0 | 1.96 | 1 | 0 |
Furrow Keratitis [description not available] | 0 | 3.05 | 5 | 0 |
Brill Disease [description not available] | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Inborn Errors of Metabolism [description not available] | 0 | 1.97 | 1 | 0 |
Metabolism, Inborn Errors Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero. | 0 | 1.97 | 1 | 0 |
Bile Duct Obstruction, Extrahepatic [description not available] | 0 | 1.97 | 1 | 0 |
Encephalitis, Venezuelan Equine [description not available] | 0 | 1.97 | 1 | 0 |
Asthenia Clinical sign or symptom manifested as debility, or lack or loss of strength and energy. | 0 | 1.97 | 1 | 0 |
Bilateral Deafness [description not available] | 0 | 1.97 | 1 | 0 |
Aseptic Meningitis [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Parotid Duct Calculi [description not available] | 0 | 1.97 | 1 | 0 |
Submandibular Gland Diseases Diseases involving the SUBMANDIBULAR GLAND. | 0 | 1.97 | 1 | 0 |
Melena The black, tarry, foul-smelling FECES that contain degraded blood. | 0 | 1.97 | 1 | 0 |
Bernard Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Biliary Tract Hemorrhage [description not available] | 0 | 1.97 | 1 | 0 |
ARC [description not available] | 0 | 1.97 | 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 | 1.97 | 1 | 0 |
Chromosomal Fragility [description not available] | 0 | 1.96 | 1 | 0 |
Broad Thumb-Hallux Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Rubinstein-Taybi Syndrome A chromosomal disorder characterized by MENTAL RETARDATION, broad thumbs, webbing of fingers and toes, beaked nose, short upper lip, pouting lower lip, agenesis of corpus callosum, large foramen magnum, keloid formation, pulmonary stenosis, vertebral anomalies, chest wall anomalies, sleep apnea, and megacolon. The disease has an autosomal dominant pattern of inheritance and is associated with deletions of the short arm of chromosome 16 (16p13.3). | 0 | 1.97 | 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 | 1.96 | 1 | 0 |
Shoulder Injuries Injuries involving the SHOULDERS and SHOULDER JOINT. | 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 |
Stammering [description not available] | 0 | 3.56 | 3 | 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 | 3.56 | 3 | 0 |
Farmer's Lung A form of alveolitis or pneumonitis due to an acquired hypersensitivity to inhaled antigens associated with farm environment. Antigens in the farm dust are commonly from bacteria actinomycetes (SACCHAROPOLYSPORA and THERMOACTINOMYCES), fungi, and animal proteins in the soil, straw, crops, pelts, serum, and excreta. | 0 | 1.96 | 1 | 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 | 1.96 | 1 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 2.35 | 2 | 0 |
Cancer of Gallbladder [description not available] | 0 | 1.94 | 1 | 0 |
Cancer of Intestines [description not available] | 0 | 1.94 | 1 | 0 |
Cancer of the Uterus [description not available] | 0 | 1.94 | 1 | 0 |
Carcinoma, Intraductal, Noninfiltrating A noninvasive (noninfiltrating) carcinoma of the breast characterized by a proliferation of malignant epithelial cells confined to the mammary ducts or lobules, without light-microscopy evidence of invasion through the basement membrane into the surrounding stroma. | 0 | 2.35 | 2 | 0 |
Gallbladder Neoplasms Tumors or cancer of the gallbladder. | 0 | 1.94 | 1 | 0 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 1.94 | 1 | 0 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 1.94 | 1 | 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 | 2.35 | 2 | 0 |
Hypergammaglobulinemia An excess of GAMMA-GLOBULINS in the serum due to chronic infections or PARAPROTEINEMIAS. | 0 | 1.94 | 1 | 0 |
Pyrosis [description not available] | 0 | 1.95 | 1 | 0 |
Heartburn Substernal pain or burning sensation, usually associated with regurgitation of gastric juice into the esophagus. | 0 | 1.95 | 1 | 0 |
Diverticulum, Meckel [description not available] | 0 | 3.27 | 2 | 0 |
Hyperesthesia Increased sensitivity to cutaneous stimulation due to a diminished threshold or an increased response to stimuli. | 0 | 1.94 | 1 | 0 |
Brain Embolism and Thrombosis [description not available] | 0 | 1.94 | 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 | 2.34 | 2 | 0 |
Bagassosis A diffuse parenchymal lung disease caused by inhaled dust from processing SUGARCANE (bagasse), usually in the manufacturing of wallboard. | 0 | 2.35 | 2 | 0 |
Silicotuberculosis Pulmonary or extrapulmonary infection caused by MYCOBACTERIUM TUBERCULOSIS or nontuberculous mycobacteria in a patient with silicosis. | 0 | 1.95 | 1 | 0 |
Pneumoconiosis A diffuse parenchymal lung disease caused by inhalation of dust and by tissue reaction to their presence. These inorganic, organic, particulate, or vaporized matters usually are inhaled by workers in their occupational environment, leading to the various forms (ASBESTOSIS; BYSSINOSIS; and others). Similar air pollution can also have deleterious effects on the general population. | 0 | 2.35 | 2 | 0 |
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 | 2.35 | 2 | 0 |
Trypanosomiasis Infection with protozoa of the genus TRYPANOSOMA. | 0 | 1.94 | 1 | 0 |
Arthus Phenomenon [description not available] | 0 | 2.35 | 2 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 2.35 | 2 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 2.35 | 2 | 0 |
Glomangioma [description not available] | 0 | 2.35 | 2 | 0 |
Infections, Reoviridae [description not available] | 0 | 2.63 | 3 | 0 |
Enlarged Liver [description not available] | 0 | 1.94 | 1 | 0 |
Dupre Syndrome [description not available] | 0 | 1.94 | 1 | 0 |
Duhring Disease [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 1.95 | 1 | 0 |
Carcinoma, Small Cell An anaplastic, highly malignant, and usually bronchogenic carcinoma composed of small ovoid cells with scanty neoplasm. It is characterized by a dominant, deeply basophilic nucleus, and absent or indistinct nucleoli. (From Stedman, 25th ed; Holland et al., Cancer Medicine, 3d ed, p1286-7) | 0 | 1.95 | 1 | 0 |
Appetite Disorders [description not available] | 0 | 2.35 | 2 | 0 |
Feeding and Eating Disorders A group of disorders characterized by physiological and psychological disturbances in appetite or food intake. | 0 | 2.35 | 2 | 0 |
Encephalitis, Japanese B [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 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 | 1.95 | 1 | 0 |
Adamantiades-Behcet Disease [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Moniliasis, Oral [description not available] | 0 | 1.95 | 1 | 0 |
Congenital Epulides [description not available] | 0 | 1.95 | 1 | 0 |
Candidiasis, Oral Infection of the mucous membranes of the mouth by a fungus of the genus CANDIDA. (Dorland, 27th ed) | 0 | 1.95 | 1 | 0 |
Envenomation, Snakebite [description not available] | 0 | 1.95 | 1 | 0 |
Uterine Rupture A complete separation or tear in the wall of the UTERUS with or without expulsion of the FETUS. It may be due to injuries, multiple pregnancies, large fetus, previous scarring, or obstruction. | 0 | 1.95 | 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 | 1.95 | 1 | 0 |
Complications, Labor [description not available] | 0 | 2.35 | 2 | 0 |
Tracheitis INFLAMMATION of the TRACHEA that is usually associated with RESPIRATORY TRACT INFECTIONS. | 0 | 3.55 | 3 | 0 |
Hemorrhage, Oral [description not available] | 0 | 1.95 | 1 | 0 |
Shock, Traumatic Shock produced as a result of trauma. | 0 | 1.94 | 1 | 0 |
Eye Burns Injury to any part of the eye by extreme heat, chemical agents, or ultraviolet radiation. | 0 | 1.95 | 1 | 0 |
Alastrim [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Insulin Sensitivity [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Brill-Symmers Disease [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Vaginal Diseases Pathological processes of the VAGINA. | 0 | 1.95 | 1 | 0 |
Curling Ulcer Acute stress DUODENAL ULCER, usually observed in patients with extensive third-degree burns. | 0 | 1.95 | 1 | 0 |
Duodenal Ulcer A PEPTIC ULCER located in the DUODENUM. | 0 | 1.95 | 1 | 0 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 3.27 | 2 | 0 |
Erythrasma A chronic bacterial infection of major folds of the skin, caused by Corynebacterium minutissimum. | 0 | 2.86 | 1 | 0 |
Water Intoxication A condition resulting from the excessive retention of water with sodium depletion. | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Endarteritis Inflammation of the inner endothelial lining (TUNICA INTIMA) of an artery. | 0 | 1.94 | 1 | 0 |
Aortitis, Syphilitic [description not available] | 0 | 1.94 | 1 | 0 |
Endometrial Diseases [description not available] | 0 | 1.94 | 1 | 0 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 1.94 | 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 | 1.95 | 1 | 0 |
Genetic Diseases [description not available] | 0 | 1.95 | 1 | 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 | 1.95 | 1 | 0 |
Cancer of Parathyroid [description not available] | 0 | 1.95 | 1 | 0 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 1.95 | 1 | 0 |
Segond Fracture [description not available] | 0 | 2.35 | 2 | 0 |
Tibial Fractures Fractures of the TIBIA. | 0 | 2.35 | 2 | 0 |
Childhood Schizophrenia [description not available] | 0 | 2.86 | 1 | 0 |
Shock, Cardiogenic Shock resulting from diminution of cardiac output in heart disease. | 0 | 2.86 | 1 | 0 |
Cranial Nerve III Injury [description not available] | 0 | 2.86 | 1 | 0 |
Di Guglielmo Disease [description not available] | 0 | 1.94 | 1 | 0 |
Leukemia, Erythroblastic, Acute A myeloproliferative disorder characterized by neoplastic proliferation of erythroblastic and myeloblastic elements with atypical erythroblasts and myeloblasts in the peripheral blood. | 0 | 1.94 | 1 | 0 |
African Horse Sickness An insect-borne reovirus infection of horses, mules and donkeys in Africa and the Middle East; characterized by pulmonary edema, cardiac involvement, and edema of the head and neck. | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Infections, Listeria [description not available] | 0 | 1.94 | 1 | 0 |
Genital Diseases, Male Pathological processes involving the male reproductive tract (GENITALIA, MALE). | 0 | 1.94 | 1 | 0 |
Acute Bacterial Prostatitis [description not available] | 0 | 1.94 | 1 | 0 |
Prostatitis Infiltration of inflammatory cells into the parenchyma of PROSTATE. The subtypes are classified by their varied laboratory analysis, clinical presentation and response to treatment. | 0 | 1.94 | 1 | 0 |
Autolysis The spontaneous disintegration of tissues or cells by the action of their own autogenous enzymes. | 0 | 1.94 | 1 | 0 |
Infections, Vibrio [description not available] | 0 | 1.94 | 1 | 0 |
Amino Acid Metabolism Disorders, Inborn [description not available] | 0 | 1.94 | 1 | 0 |
Poisoning, Mercury [description not available] | 0 | 1.94 | 1 | 0 |
Cecal Diseases Pathological developments in the CECUM. | 0 | 1.94 | 1 | 0 |
Mercury Poisoning Poisoning that results from chronic or acute ingestion, injection, inhalation, or skin absorption of MERCURY or MERCURY COMPOUNDS. | 0 | 1.94 | 1 | 0 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 2.35 | 2 | 0 |
Cattle Plague [description not available] | 0 | 1.94 | 1 | 0 |
Urethritis Inflammation involving the URETHRA. Similar to CYSTITIS, clinical symptoms range from vague discomfort to painful urination (DYSURIA), urethral discharge, or both. | 0 | 1.94 | 1 | 0 |
Hyperactivity, Motor [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Infant Malnutrition Malnutrition, occurring in infants ages 1 month to 24 months, which is due to insufficient intake of food, dietary nutrients, or a pathophysiologic condition which prevents the absorption and utilization of food. Growth and development are markedly affected. | 0 | 1.94 | 1 | 0 |
Bejel [description not available] | 0 | 1.94 | 1 | 0 |
Hemorrhage, Peptic Ulcer [description not available] | 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 |
Anemia, Splenic [description not available] | 0 | 1.94 | 1 | 0 |
African Swine Fever A sometimes fatal ASFIVIRUS infection of pigs, characterized by fever, cough, diarrhea, hemorrhagic lymph nodes, and edema of the gallbladder. It is transmitted between domestic swine by direct contact, ingestion of infected meat, or fomites, or mechanically by biting flies or soft ticks (genus Ornithodoros). | 0 | 1.94 | 1 | 0 |
Lentiginosis, Perioral [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Amelogenesis Imperfecta A clinically and genetically heterogeneous group of hereditary conditions characterized by malformed DENTAL ENAMEL, usually involving DENTAL ENAMEL HYPOPLASIA and/or TOOTH HYPOMINERALIZATION. | 0 | 1.94 | 1 | 0 |
Kidney, Polycystic [description not available] | 0 | 1.94 | 1 | 0 |
Corpus Luteum Cyst [description not available] | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Ovarian Cysts General term for CYSTS and cystic diseases of the OVARY. | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 1.94 | 1 | 0 |
Cane-Cutter Fever [description not available] | 0 | 1.94 | 1 | 0 |
Leptospirosis Infections with bacteria of the genus LEPTOSPIRA. | 0 | 1.94 | 1 | 0 |
Bacteroides Infections Infections with bacteria of the genus BACTEROIDES. | 0 | 1.94 | 1 | 0 |
Empyema Presence of pus in a hollow organ or body cavity. | 0 | 1.94 | 1 | 0 |
Dominant Hereditary Sensory Neuropathy, Type III [description not available] | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Brain Ventricular Neoplasms [description not available] | 0 | 1.94 | 1 | 0 |
Humeral Fractures Fractures of the HUMERUS. | 0 | 1.94 | 1 | 0 |
Radius Fractures Fractures of the RADIUS. | 0 | 1.94 | 1 | 0 |
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 | 1.94 | 1 | 0 |
Abdominal Cramps [description not available] | 0 | 1.94 | 1 | 0 |