Condition | Indicated | Relationship Strength | Studies | Trials |
Cirrhosis [description not available] | 0 | 27.05 | 575 | 23 |
Biliary Cirrhosis [description not available] | 0 | 3.33 | 1 | 0 |
Cardiomyopathies, Primary [description not available] | 0 | 20.22 | 403 | 14 |
Fibrosis Any pathological condition where fibrous connective tissue invades any organ, usually as a consequence of inflammation or other injury. | 0 | 22.05 | 575 | 23 |
Liver Cirrhosis, Biliary FIBROSIS of the hepatic parenchyma due to obstruction of BILE flow (CHOLESTASIS) in the intrahepatic or extrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC; BILE DUCTS, EXTRAHEPATIC). Primary biliary cholangitis involves the destruction of small intra-hepatic bile ducts and decreased bile secretion. Secondary biliary cholangitis is produced by prolonged obstruction of large intrahepatic or extrahepatic bile ducts from a variety of causes. | 0 | 3.33 | 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 | 20.22 | 403 | 14 |
Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. | 0 | 13.96 | 278 | 1 |
MS (Multiple Sclerosis) [description not available] | 0 | 20.86 | 345 | 54 |
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 | 20.86 | 345 | 54 |
Birth Weight The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. | 0 | 3.7 | 1 | 1 |
Fetal Growth Restriction [description not available] | 0 | 3.81 | 2 | 1 |
Fetal Growth Retardation Failure of a FETUS to attain expected GROWTH. | 0 | 3.81 | 2 | 1 |
Pregnancy The status during which female mammals carry their developing young (EMBRYOS or FETUSES) in utero before birth, beginning from FERTILIZATION to BIRTH. | 0 | 14.91 | 112 | 1 |
Familial Precocious Puberty [description not available] | 0 | 2.72 | 2 | 0 |
Anesthesia A state characterized by loss of feeling or sensation. This depression of nerve function is usually the result of pharmacologic action and is induced to allow performance of surgery or other painful procedures. | 0 | 10.51 | 8 | 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 | 2.72 | 2 | 0 |
Cardiomyopathy, Hypertrophic Obstructive [description not available] | 0 | 17.76 | 247 | 13 |
Cardiomyopathy, Hypertrophic A form of CARDIAC MUSCLE disease, characterized by left and/or right ventricular hypertrophy (HYPERTROPHY, LEFT VENTRICULAR; HYPERTROPHY, RIGHT VENTRICULAR), frequent asymmetrical involvement of the HEART SEPTUM, and normal or reduced left ventricular volume. Risk factors include HYPERTENSION; AORTIC STENOSIS; and gene MUTATION; (FAMILIAL HYPERTROPHIC CARDIOMYOPATHY). | 0 | 17.76 | 247 | 13 |
Diabetes Mellitus, Adult-Onset [description not available] | 0 | 6.67 | 11 | 1 |
Cardiac Aneurysm [description not available] | 0 | 3.59 | 8 | 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 | 6.67 | 11 | 1 |
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 | 15.43 | 201 | 5 |
Cardiovascular Stroke [description not available] | 0 | 20.83 | 510 | 26 |
Cicatrix The fibrous tissue that replaces normal tissue during the process of WOUND HEALING. | 0 | 15.43 | 201 | 5 |
Myocardial Infarction NECROSIS of the MYOCARDIUM caused by an obstruction of the blood supply to the heart (CORONARY CIRCULATION). | 0 | 20.83 | 510 | 26 |
ST Elevated Myocardial Infarction [description not available] | 0 | 14.11 | 76 | 10 |
ST Elevation Myocardial Infarction A clinical syndrome defined by MYOCARDIAL ISCHEMIA symptoms; persistent elevation in the ST segments of the ELECTROCARDIOGRAM; and release of BIOMARKERS of myocardial NECROSIS (e.g., elevated TROPONIN levels). ST segment elevation in the ECG is often used in determining the treatment protocol (see also NON-ST ELEVATION MYOCARDIAL INFARCTION). | 0 | 14.11 | 76 | 10 |
Allergy, Drug [description not available] | 0 | 18.03 | 107 | 27 |
Delayed Hypersensitivity [description not available] | 0 | 2.71 | 3 | 0 |
Drug Hypersensitivity Immunologically mediated adverse reactions to medicinal substances used legally or illegally. | 0 | 18.03 | 107 | 27 |
Erythema Redness of the skin produced by congestion of the capillaries. This condition may result from a variety of disease processes. | 0 | 7.66 | 2 | 0 |
Left Ventricular Dysfunction [description not available] | 0 | 19.14 | 218 | 27 |
Aortic Stenosis [description not available] | 0 | 10.79 | 41 | 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 | 10.79 | 41 | 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 | 19.14 | 218 | 27 |
Carditis [description not available] | 0 | 17.03 | 287 | 1 |
Acute Disease Disease having a short and relatively severe course. | 0 | 15.9 | 164 | 5 |
Myocarditis Inflammatory processes of the muscular walls of the heart (MYOCARDIUM) which result in injury to the cardiac muscle cells (MYOCYTES, CARDIAC). Manifestations range from subclinical to sudden death (DEATH, SUDDEN). Myocarditis in association with cardiac dysfunction is classified as inflammatory CARDIOMYOPATHY usually caused by INFECTION, autoimmune diseases, or responses to toxic substances. Myocarditis is also a common cause of DILATED CARDIOMYOPATHY and other cardiomyopathies. | 0 | 17.03 | 287 | 1 |
Anterior Fascicular Block [description not available] | 0 | 5.81 | 11 | 0 |
Arrhythmia [description not available] | 0 | 14.65 | 126 | 6 |
Mitral Incompetence [description not available] | 0 | 6.71 | 17 | 0 |
Click-Murmur Syndrome [description not available] | 0 | 7.32 | 19 | 0 |
Arrhythmias, Cardiac Any disturbances of the normal rhythmic beating of the heart or MYOCARDIAL CONTRACTION. Cardiac arrhythmias can be classified by the abnormalities in HEART RATE, disorders of electrical impulse generation, or impulse conduction. | 0 | 14.65 | 126 | 6 |
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 | 6.71 | 17 | 0 |
Endolymphatic Hydrops An accumulation of ENDOLYMPH in the inner ear (LABYRINTH) leading to buildup of pressure and distortion of intralabyrinthine structures, such as COCHLEA and SEMICIRCULAR CANALS. It is characterized by SENSORINEURAL HEARING LOSS; TINNITUS; and sometimes VERTIGO. | 0 | 10.99 | 79 | 4 |
Auditory Vertigo [description not available] | 0 | 11.32 | 74 | 7 |
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 | 16.32 | 74 | 7 |
Devic Disease [description not available] | 0 | 7.99 | 17 | 1 |
Local Neoplasm Recurrence [description not available] | 0 | 13.16 | 83 | 3 |
Neuromyelitis Optica A syndrome characterized by acute OPTIC NEURITIS; MYELITIS, TRANSVERSE; demyelinating and/or necrotizing lesions in the OPTIC NERVES and SPINAL CORD; and presence of specific autoantibodies to AQUAPORIN 4. | 0 | 7.99 | 17 | 1 |
Heart Disease, Ischemic [description not available] | 0 | 15.87 | 130 | 6 |
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 | 15.87 | 130 | 6 |
Arrhythmogenic Right Ventricular Cardiomyopathy [description not available] | 0 | 6.44 | 24 | 0 |
Arrhythmogenic Right Ventricular Dysplasia A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial cells. Primary injuries usually are at the free wall of right ventricular and right atria resulting in ventricular and supraventricular arrhythmias. | 0 | 6.44 | 24 | 0 |
Cardiomyopathy, Congestive [description not available] | 0 | 18.19 | 162 | 21 |
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 | 18.19 | 162 | 21 |
Arteriosclerosis, Coronary [description not available] | 0 | 17.45 | 111 | 26 |
Coronary Artery Disease Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause. | 0 | 17.45 | 111 | 26 |
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 | 6.22 | 52 | 0 |
Joint Pain [description not available] | 0 | 3.52 | 7 | 0 |
Anterior Cervical Pain [description not available] | 0 | 5.39 | 9 | 0 |
Arthralgia Pain in the joint. | 0 | 3.52 | 7 | 0 |
Neck Pain Discomfort or more intense forms of pain that are localized to the cervical region. This term generally refers to pain in the posterior or lateral regions of the neck. | 0 | 5.39 | 9 | 0 |
Osteoarthritis of Knee [description not available] | 0 | 8.61 | 18 | 2 |
Plica Syndrome [description not available] | 0 | 8.25 | 38 | 3 |
Synovitis Inflammation of the SYNOVIAL MEMBRANE. | 0 | 8.25 | 38 | 3 |
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 | 8.61 | 18 | 2 |
Benign Neoplasms [description not available] | 0 | 16.03 | 288 | 3 |
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 | 16.03 | 288 | 3 |
Carcinoma, Non-Small Cell Lung [description not available] | 0 | 5.11 | 15 | 0 |
Cancer of Lung [description not available] | 0 | 11.66 | 76 | 1 |
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 | 5.11 | 15 | 0 |
Lung Neoplasms Tumors or cancer of the LUNG. | 0 | 11.66 | 76 | 1 |
Bechterew Syndrome [description not available] | 0 | 3.07 | 4 | 0 |
Arthritis, Spinal [description not available] | 0 | 3.38 | 6 | 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 | 23.09 | 902 | 86 |
Spondylarthropathies Heterogeneous group of arthritic diseases sharing clinical and radiologic features. They are associated with the HLA-B27 ANTIGEN and some with a triggering infection. Most involve the axial joints in the SPINE, particularly the SACROILIAC JOINT, but can also involve asymmetric peripheral joints. Subsets include ANKYLOSING SPONDYLITIS; REACTIVE ARTHRITIS; PSORIATIC ARTHRITIS; and others. | 0 | 3.07 | 4 | 0 |
Apoplexy [description not available] | 0 | 12.97 | 71 | 3 |
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 | 12.97 | 71 | 3 |
Auricular Fibrillation [description not available] | 0 | 15.93 | 160 | 9 |
Atrial Septal Defect [description not available] | 0 | 7.95 | 4 | 0 |
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 | 15.93 | 160 | 9 |
Recrudescence [description not available] | 0 | 17.65 | 142 | 23 |
Atrioventricular Nodal Re-Entrant Tachycardia [description not available] | 0 | 13.67 | 100 | 5 |
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 | 13.67 | 100 | 5 |
Aortitis Syndrome [description not available] | 0 | 3.55 | 8 | 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 | 8.55 | 8 | 0 |
2019 Novel Coronavirus Disease [description not available] | 0 | 13.07 | 106 | 0 |
Muscular Dystrophy [description not available] | 0 | 3.26 | 6 | 0 |
Cardiomyopathy, Restrictive A form of CARDIAC MUSCLE disease in which the ventricular walls are excessively rigid, impeding ventricular filling. It is marked by reduced diastolic volume of either or both ventricles but normal or nearly normal systolic function. It may be idiopathic or associated with other diseases (ENDOMYOCARDIAL FIBROSIS or AMYLOIDOSIS) causing interstitial fibrosis. | 0 | 3.3 | 4 | 0 |
Muscular Dystrophies A heterogeneous group of inherited MYOPATHIES, characterized by wasting and weakness of the SKELETAL MUSCLE. They are categorized by the sites of MUSCLE WEAKNESS; AGE OF ONSET; and INHERITANCE PATTERNS. | 0 | 3.26 | 6 | 0 |
Benign Neoplasms, Brain [description not available] | 0 | 20.5 | 485 | 54 |
Astrocytoma, Grade IV [description not available] | 0 | 12.78 | 93 | 5 |
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 | 20.5 | 485 | 54 |
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 | 12.78 | 93 | 5 |
Cardiac Failure [description not available] | 0 | 18.84 | 189 | 21 |
AL Amyloidosis [description not available] | 0 | 4.61 | 7 | 0 |
Immunoglobulin Light-chain Amyloidosis A nonproliferative disorder of the PLASMA CELL characterized by excessive production and misfolding of IMMUNOGLOBULIN LIGHT CHAINS that form insoluble amyloid fibrils (see AMYLOID DEPOSITS) in various tissues. Clinical features include LIVER FAILURE; MULTIPLE MYELOMA; NEPHROTIC SYNDROME; RESTRICTIVE CARDIOMYOPATHY, and neuropathies. | 0 | 4.61 | 7 | 0 |
Amyloidosis A group of sporadic, familial and/or inherited, degenerative, and infectious disease processes, linked by the common theme of abnormal protein folding and deposition of AMYLOID. As the amyloid deposits enlarge they displace normal tissue structures, causing disruption of function. Various signs and symptoms depend on the location and size of the deposits. | 0 | 10.42 | 61 | 1 |
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 | 18.84 | 189 | 21 |
chronic COVID syndrome [description not available] | 0 | 3.07 | 3 | 0 |
Adenocarcinoma, Basal Cell [description not available] | 0 | 11.54 | 79 | 2 |
Cardiac Cancer [description not available] | 0 | 6.3 | 24 | 0 |
Metastase [description not available] | 0 | 9.06 | 36 | 2 |
Adenocarcinoma A malignant epithelial tumor with a glandular organization. | 0 | 11.54 | 79 | 2 |
Neoplasm Metastasis The transfer of a neoplasm from one organ or part of the body to another remote from the primary site. | 0 | 9.06 | 36 | 2 |
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 | 6.88 | 25 | 1 |
Encephalitis, JC Polyomavirus [description not available] | 0 | 5.16 | 16 | 0 |
Leukoencephalopathy, Progressive Multifocal An opportunistic viral infection of the central nervous system associated with conditions that impair cell-mediated immunity (e.g., ACQUIRED IMMUNODEFICIENCY SYNDROME and other IMMUNOLOGIC DEFICIENCY SYNDROMES; HEMATOLOGIC NEOPLASMS; IMMUNOSUPPRESSION; and COLLAGEN DISEASES). The causative organism is JC Polyomavirus (JC VIRUS) which primarily affects oligodendrocytes, resulting in multiple areas of demyelination. Clinical manifestations include DEMENTIA; ATAXIA; visual disturbances; and other focal neurologic deficits, generally progressing to a vegetative state within 6 months. (From Joynt, Clinical Neurology, 1996, Ch26, pp36-7) | 0 | 5.16 | 16 | 0 |
Becker Muscular Dystrophy [description not available] | 0 | 11.91 | 35 | 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 | 6.91 | 35 | 0 |
Fallot's Tetralogy [description not available] | 0 | 7.1 | 17 | 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 | 7.1 | 17 | 0 |
Besnier-Boeck Disease [description not available] | 0 | 12.06 | 95 | 1 |
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 | 12.06 | 95 | 1 |
Inflammatory Response Syndrome, Systemic [description not available] | 0 | 5.64 | 9 | 0 |
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 | 5.64 | 9 | 0 |
Carcinomatous Meningitis [description not available] | 0 | 4.18 | 5 | 0 |
Pachymeningitis [description not available] | 0 | 5.87 | 14 | 0 |
Kahler Disease [description not available] | 0 | 5.12 | 17 | 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 | 10.87 | 14 | 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 | 5.12 | 17 | 0 |
Meningeal Carcinomatosis Primary or secondary neoplasm in the ARACHNOID or SUBARACHNOID SPACE. It appears as a diffuse fibrotic thickening of the MENINGES associated with variable degrees of inflammation. | 0 | 4.18 | 5 | 0 |
Atherogenesis [description not available] | 0 | 7.22 | 47 | 0 |
Atherosclerosis A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. | 0 | 7.22 | 47 | 0 |
DRESS Syndrome [description not available] | 0 | 7.41 | 1 | 0 |
Cancer of Pituitary [description not available] | 0 | 11.65 | 76 | 5 |
Craniopharyngioma, Adamantinous [description not available] | 0 | 5.56 | 9 | 2 |
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 | 5.56 | 9 | 2 |
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 | 11.65 | 76 | 5 |
Nephrogenic Systemic Fibrosis [description not available] | 0 | 18.26 | 297 | 3 |
Nephrogenic Fibrosing Dermopathy A chronic, acquired, idiopathic, progressive eruption of the skin that occurs in the context of RENAL FAILURE. It is sometimes accompanied by systemic fibrosis. The pathogenesis seems to be multifactorial, with postulated involvement of circulating fibrocytes. There is a strong association between this disorder and the use of gadolinium-based contrast agents. | 0 | 18.26 | 297 | 3 |
Extrasystole, Ventricular [description not available] | 0 | 10.16 | 27 | 9 |
Shingles [description not available] | 0 | 2.73 | 3 | 0 |
Brachial Paresis [description not available] | 0 | 4.02 | 13 | 0 |
Nerve Root Avulsion [description not available] | 0 | 4.83 | 12 | 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 | 2.73 | 3 | 0 |
Radiculopathy Disease involving a spinal nerve root (see SPINAL NERVE ROOTS) which may result from compression related to INTERVERTEBRAL DISK DISPLACEMENT; SPINAL CORD INJURIES; SPINAL DISEASES; and other conditions. Clinical manifestations include radicular pain, weakness, and sensory loss referable to structures innervated by the involved nerve root. | 0 | 9.83 | 12 | 0 |
Shock, Cardiogenic Shock resulting from diminution of cardiac output in heart disease. | 0 | 2.8 | 3 | 0 |
Sicca Syndrome [description not available] | 0 | 3.29 | 6 | 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 | 3.29 | 6 | 0 |
Bleeding [description not available] | 0 | 8.08 | 27 | 0 |
Hemorrhage Bleeding or escape of blood from a vessel. | 0 | 8.08 | 27 | 0 |
Glial Cell Tumors [description not available] | 0 | 14.71 | 157 | 5 |
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 | 14.71 | 157 | 5 |
Disease Exacerbation [description not available] | 0 | 18.91 | 183 | 28 |
Constriction, Pathological [description not available] | 0 | 6.32 | 35 | 1 |
Constriction, Pathologic The condition of an anatomical structure's being constricted beyond normal dimensions. | 0 | 6.32 | 35 | 1 |
Cochlear Hearing Loss [description not available] | 0 | 8.76 | 33 | 2 |
Bacterial Meningitides [description not available] | 0 | 4.93 | 8 | 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 | 8.76 | 33 | 2 |
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 | 4.93 | 8 | 1 |
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 | 19.9 | 129 | 4 |
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 | 14.9 | 129 | 4 |
Orphan Diseases Rare diseases that have not been well studied. | 0 | 5.34 | 12 | 0 |
Infectious Myelitis [description not available] | 0 | 6.62 | 11 | 1 |
Chronic Inflammatory Demyelinating Polyradiculoneuropathy [description not available] | 0 | 3.53 | 7 | 0 |
Polyradiculitis [description not available] | 0 | 4.56 | 9 | 0 |
Polyradiculopathy Disease or injury involving multiple SPINAL NERVE ROOTS. Polyradiculitis refers to inflammation of multiple spinal nerve roots. | 0 | 4.56 | 9 | 0 |
Polyradiculoneuropathy, Chronic Inflammatory Demyelinating A slowly progressive autoimmune demyelinating disease of peripheral nerves and nerve roots. Clinical manifestations include weakness and sensory loss in the extremities and enlargement of peripheral nerves. The course may be relapsing-remitting or demonstrate a step-wise progression. Protein is usually elevated in the spinal fluid and cranial nerves are typically spared. GUILLAIN-BARRE SYNDROME features a relatively rapid progression of disease which distinguishes it from this condition. (Adams et al., Principles of Neurology, 6th ed, p1337) | 0 | 3.53 | 7 | 0 |
Congenital Myotonic Dystrophy [description not available] | 0 | 3.05 | 4 | 0 |
Facio-Scapulo-Humeral Dystrophy [description not available] | 0 | 2.31 | 1 | 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 | 3.05 | 4 | 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 | 2.31 | 1 | 0 |
Adult Optic Nerve Glioma [description not available] | 0 | 3.2 | 5 | 0 |
Optic Nerve Glioma Glial cell derived tumors arising from the optic nerve, usually presenting in childhood. | 0 | 3.2 | 5 | 0 |
Anasarca [description not available] | 0 | 12.05 | 71 | 4 |
Cardiac Arrest, Sudden [description not available] | 0 | 16.96 | 119 | 15 |
Out-of-Hospital Cardiac Arrest Occurrence of heart arrest in an individual when there is no immediate access to medical personnel or equipment. | 0 | 2.31 | 1 | 0 |
Edema Abnormal fluid accumulation in TISSUES or body cavities. Most cases of edema are present under the SKIN in SUBCUTANEOUS TISSUE. | 0 | 12.05 | 71 | 4 |
Death, Sudden, Cardiac Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005) | 0 | 16.96 | 119 | 15 |
Genetic Diseases, X-Chromosome Linked [description not available] | 0 | 2.53 | 2 | 0 |
Amaurosis [description not available] | 0 | 2.92 | 4 | 0 |
Nervous System Disorders [description not available] | 0 | 7.67 | 15 | 1 |
Cryptogenic Infantile Spasms [description not available] | 0 | 2.45 | 2 | 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 | 2.92 | 4 | 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 | 7.67 | 15 | 1 |
Retinal Degeneration A retrogressive pathological change in the retina, focal or generalized, caused by genetic defects, inflammation, trauma, vascular disease, or aging. Degeneration affecting predominantly the macula lutea of the retina is MACULAR DEGENERATION. (Newell, Ophthalmology: Principles and Concepts, 7th ed, p304) | 0 | 2.41 | 1 | 0 |
Spasms, Infantile An epileptic syndrome characterized by the triad of infantile spasms, hypsarrhythmia, and arrest of psychomotor development at seizure onset. The majority present between 3-12 months of age, with spasms consisting of combinations of brief flexor or extensor movements of the head, trunk, and limbs. The condition is divided into two forms: cryptogenic (idiopathic) and symptomatic (secondary to a known disease process such as intrauterine infections; nervous system abnormalities; BRAIN DISEASES, METABOLIC, INBORN; prematurity; perinatal asphyxia; TUBEROUS SCLEROSIS; etc.). (From Menkes, Textbook of Child Neurology, 5th ed, pp744-8) | 0 | 2.45 | 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 | 9.81 | 11 | 0 |
Myelopathy [description not available] | 0 | 10.01 | 44 | 2 |
Diffuse Large B-Cell Lymphoma [description not available] | 0 | 3.59 | 8 | 0 |
Intradural-Extramedullary Spinal Cord Neoplasms [description not available] | 0 | 9.74 | 71 | 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 | 10.01 | 44 | 2 |
Spinal Cord Neoplasms Benign and malignant neoplasms which occur within the substance of the spinal cord (intramedullary neoplasms) or in the space between the dura and spinal cord (intradural extramedullary neoplasms). The majority of intramedullary spinal tumors are primary CNS neoplasms including ASTROCYTOMA; EPENDYMOMA; and LIPOMA. Intramedullary neoplasms are often associated with SYRINGOMYELIA. The most frequent histologic types of intradural-extramedullary tumors are MENINGIOMA and NEUROFIBROMA. | 0 | 9.74 | 71 | 1 |
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 | 3.59 | 8 | 0 |
Allergic Reaction [description not available] | 0 | 5.26 | 11 | 0 |
Hypersensitivity Altered reactivity to an antigen, which can result in pathologic reactions upon subsequent exposure to that particular antigen. | 0 | 5.26 | 11 | 0 |
Breast Cancer [description not available] | 0 | 15.12 | 211 | 4 |
Breast Neoplasms Tumors or cancer of the human BREAST. | 0 | 15.12 | 211 | 4 |
Left Ventricular Hypertrophy [description not available] | 0 | 11.29 | 70 | 0 |
Blood Pressure, High [description not available] | 0 | 8.24 | 33 | 0 |
Hypertension Persistently high systemic arterial BLOOD PRESSURE. Based on multiple readings (BLOOD PRESSURE DETERMINATION), hypertension is currently defined as when SYSTOLIC PRESSURE is consistently greater than 140 mm Hg or when DIASTOLIC PRESSURE is consistently 90 mm Hg or more. | 0 | 8.24 | 33 | 0 |
Hypertrophy, Left Ventricular Enlargement of the LEFT VENTRICLE of the heart. This increase in ventricular mass is attributed to sustained abnormal pressure or volume loads and is a contributor to cardiovascular morbidity and mortality. | 0 | 11.29 | 70 | 0 |
Acute Relapsing Multiple Sclerosis [description not available] | 0 | 19.57 | 173 | 81 |
Acute Post-Traumatic Stress Disorder [description not available] | 0 | 2.41 | 1 | 0 |
Stress Disorders, Post-Traumatic A class of traumatic stress disorders with symptoms that last more than one month. | 0 | 2.41 | 1 | 0 |
Multiple Sclerosis, Relapsing-Remitting The most common clinical variant of MULTIPLE SCLEROSIS, characterized by recurrent acute exacerbations of neurologic dysfunction followed by partial or complete recovery. Common clinical manifestations include loss of visual (see OPTIC NEURITIS), motor, sensory, or bladder function. Acute episodes of demyelination may occur at any site in the central nervous system, and commonly involve the optic nerves, spinal cord, brain stem, and cerebellum. (Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 19.57 | 173 | 81 |
Cardiac Toxicity [description not available] | 0 | 3.54 | 5 | 0 |
Cancer of Esophagus [description not available] | 0 | 4.41 | 7 | 0 |
Esophageal Neoplasms Tumors or cancer of the ESOPHAGUS. | 0 | 4.41 | 7 | 0 |
Cardiotoxicity Damage to the HEART or its function secondary to exposure to toxic substances such as drugs used in CHEMOTHERAPY; IMMUNOTHERAPY; or RADIATION. | 0 | 3.54 | 5 | 0 |
Apical Ballooning Syndrome [description not available] | 0 | 6.73 | 32 | 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 | 6.73 | 32 | 0 |
Adamantiades-Behcet Disease [description not available] | 0 | 3.13 | 5 | 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 | 3.13 | 5 | 0 |
Inflammatory Pseudotumor [description not available] | 0 | 9.22 | 6 | 0 |
Cancer of Nasopharynx [description not available] | 0 | 7.49 | 21 | 1 |
Granuloma, Plasma Cell A slow-growing benign pseudotumor in which plasma cells greatly outnumber the inflammatory cells. | 0 | 4.22 | 6 | 0 |
Nasopharyngeal Neoplasms Tumors or cancer of the NASOPHARYNX. | 0 | 7.49 | 21 | 1 |
Atheroma [description not available] | 0 | 11.25 | 36 | 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 | 9.47 | 8 | 0 |
Cardiac Remodeling, Ventricular [description not available] | 0 | 14.32 | 96 | 2 |
Chronic Progressive Multiple Sclerosis [description not available] | 0 | 12.28 | 24 | 14 |
Innate Inflammatory Response [description not available] | 0 | 15.62 | 154 | 8 |
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 | 15.62 | 154 | 8 |
Multiple Sclerosis, Chronic Progressive A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914) | 0 | 12.28 | 24 | 14 |
Atopic Hypersensitivity [description not available] | 0 | 7.96 | 13 | 1 |
Demyelinative Myelitis [description not available] | 0 | 3.85 | 11 | 0 |
CACH Syndrome [description not available] | 0 | 2.69 | 2 | 0 |
Degenerative Diseases, Central Nervous System [description not available] | 0 | 5.6 | 4 | 0 |
Central Nervous System Disease [description not available] | 0 | 16.82 | 64 | 37 |
Atrophy Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes. | 0 | 9.34 | 29 | 3 |
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 | 16.82 | 64 | 37 |
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 | 5.6 | 4 | 0 |
Aneurysm, Anterior Cerebral Artery [description not available] | 0 | 7.18 | 33 | 1 |
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 | 7.18 | 33 | 1 |
ACL Injuries [description not available] | 0 | 3.02 | 4 | 0 |
Allodynia [description not available] | 0 | 3.22 | 3 | 0 |
Arthritis, Degenerative [description not available] | 0 | 6.65 | 19 | 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 | 6.65 | 19 | 0 |
Bacterial Disease [description not available] | 0 | 5.36 | 13 | 0 |
Bacterial Infections Infections by bacteria, general or unspecified. | 0 | 5.36 | 13 | 0 |
Experimental Hepatoma [description not available] | 0 | 4.85 | 33 | 0 |
Experimental Neoplasms [description not available] | 0 | 7.89 | 80 | 0 |
Cardiac Diseases [description not available] | 0 | 15.83 | 117 | 3 |
Heart Diseases Pathological conditions involving the HEART including its structural and functional abnormalities. | 0 | 15.83 | 117 | 3 |
Colitis, Granulomatous [description not available] | 0 | 9.03 | 29 | 3 |
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 | 9.03 | 29 | 3 |
Injuries, Spinal Cord [description not available] | 0 | 5.22 | 11 | 0 |
Spinal Cord Injuries Penetrating and non-penetrating injuries to the spinal cord resulting from traumatic external forces (e.g., WOUNDS, GUNSHOT; WHIPLASH INJURIES; etc.). | 0 | 5.22 | 11 | 0 |
Immune Reconstitution Disease [description not available] | 0 | 2.87 | 3 | 0 |
Myofascial Trigger Point Pain [description not available] | 0 | 2.41 | 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 | 2.41 | 1 | 0 |
Aortic Valve Disease 1 [description not available] | 0 | 2.76 | 2 | 0 |
Bilateral Superior Caval Veins [description not available] | 0 | 2.41 | 1 | 0 |
Fistula Abnormal communication most commonly seen between two internal organs, or between an internal organ and the surface of the body. | 0 | 6.26 | 12 | 1 |
Bicuspid Aortic Valve Disease Congenital heart valve defects where the AORTIC VALVE has two instead of normal three cusps. It is often associated with AORTIC REGURGITATION and AORTIC INSUFFICIENCY. | 0 | 2.76 | 2 | 0 |
Leukocytopenia [description not available] | 0 | 2.41 | 1 | 0 |
Leukopenia A decrease in the number of LEUKOCYTES in a blood sample below the normal range (LEUKOCYTE COUNT less than 4000). | 0 | 7.41 | 1 | 0 |
Hypophosphatemia A condition of an abnormally low level of PHOSPHATES in the blood. | 0 | 2.9 | 3 | 0 |
Body Weight The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. | 0 | 6.81 | 23 | 1 |
Aging The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time. | 0 | 4.36 | 20 | 0 |
Sclerosis, Systemic [description not available] | 0 | 9.4 | 45 | 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 | 9.4 | 45 | 0 |
Bilateral Deafness [description not available] | 0 | 3.4 | 2 | 0 |
Autoimmune Diseases of the Nervous System Disorders caused by cellular or humoral immune responses primarily directed towards nervous system autoantigens. The immune response may be directed towards specific tissue components (e.g., myelin) and may be limited to the central nervous system (e.g., MULTIPLE SCLEROSIS) or the peripheral nervous system (e.g., GUILLAIN-BARRE SYNDROME). | 0 | 4.66 | 5 | 0 |
ARSA Deficiency [description not available] | 0 | 2.46 | 2 | 0 |
Concomitant Strabismus [description not available] | 0 | 2.44 | 2 | 0 |
Leukodystrophy, Metachromatic An autosomal recessive metabolic disease caused by a deficiency of CEREBROSIDE-SULFATASE leading to intralysosomal accumulation of cerebroside sulfate (SULFOGLYCOSPHINGOLIPIDS) in the nervous system and other organs. Pathological features include diffuse demyelination, and metachromatically-staining granules in many cell types such as the GLIAL CELLS. There are several allelic and nonallelic forms with a variety of neurological symptoms. | 0 | 2.46 | 2 | 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 | 2.44 | 2 | 0 |
ALCAPA [description not available] | 0 | 2.41 | 1 | 0 |
Benign Meningeal Neoplasms [description not available] | 0 | 10.39 | 85 | 2 |
Meningeal Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the meningeal coverings of the brain and spinal cord. | 0 | 10.39 | 85 | 2 |
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 | 3.12 | 4 | 0 |
Central Nervous System Origin Vertigo [description not available] | 0 | 4.12 | 15 | 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 | 4.12 | 15 | 0 |
Abnormalities, Autosome [description not available] | 0 | 2.96 | 4 | 0 |
Amyloid Neuropathy Type 1 [description not available] | 0 | 6.36 | 11 | 0 |
Endomyocardial Fibrosis A condition characterized by the thickening of the ventricular ENDOCARDIUM and subendocardium (MYOCARDIUM), seen mostly in children and young adults in the TROPICAL CLIMATE. The fibrous tissue extends from the apex toward and often involves the HEART VALVES causing restrictive blood flow into the respective ventricles (CARDIOMYOPATHY, RESTRICTIVE). | 0 | 5.86 | 21 | 0 |
Amyloid Neuropathies, Familial Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN. | 0 | 6.36 | 11 | 0 |
Ganglioglioma Rare indolent tumors comprised of neoplastic glial and neuronal cells which occur primarily in children and young adults. Benign lesions tend to be associated with long survival unless the tumor degenerates into a histologically malignant form. They tend to occur in the optic nerve and white matter of the brain and spinal cord. | 0 | 3.66 | 9 | 0 |
Extravascular Hemolysis [description not available] | 0 | 4.21 | 16 | 0 |
Hemolysis The destruction of ERYTHROCYTES by many different causal agents such as antibodies, bacteria, chemicals, temperature, and changes in tonicity. | 0 | 4.21 | 16 | 0 |
Cardiovascular Diseases Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM. | 0 | 12.43 | 60 | 0 |
Cancer of Pancreas [description not available] | 0 | 11.64 | 62 | 3 |
Pancreatic Cyst A true cyst of the PANCREAS, distinguished from the much more common PANCREATIC PSEUDOCYST by possessing a lining of mucous EPITHELIUM. Pancreatic cysts are categorized as congenital, retention, neoplastic, parasitic, enterogenous, or dermoid. Congenital cysts occur more frequently as solitary cysts but may be multiple. Retention cysts are gross enlargements of PANCREATIC DUCTS secondary to ductal obstruction. (From Bockus Gastroenterology, 4th ed, p4145) | 0 | 7.46 | 2 | 0 |
Pancreatic Neoplasms Tumors or cancer of the PANCREAS. Depending on the types of ISLET CELLS present in the tumors, various hormones can be secreted: GLUCAGON from PANCREATIC ALPHA CELLS; INSULIN from PANCREATIC BETA CELLS; and SOMATOSTATIN from the SOMATOSTATIN-SECRETING CELLS. Most are malignant except the insulin-producing tumors (INSULINOMA). | 0 | 11.64 | 62 | 3 |
Abscess Accumulation of purulent material in tissues, organs, or circumscribed spaces, usually associated with signs of infection. | 0 | 5.87 | 23 | 0 |
Pleuropericarditis Inflammation of both the PERICARDIUM and the PLEURA. | 0 | 6.63 | 15 | 0 |
Pericarditis Inflammation of the PERICARDIUM from various origins, such as infection, neoplasm, autoimmune process, injuries, or drug-induced. Pericarditis usually leads to PERICARDIAL EFFUSION, or CONSTRICTIVE PERICARDITIS. | 0 | 6.63 | 15 | 0 |
Tuberculoma A tumor-like mass resulting from the enlargement of a tuberculous lesion. | 0 | 8.85 | 4 | 0 |
Dermatomyositis, Adult Type [description not available] | 0 | 2.82 | 2 | 0 |
Chylopericardium [description not available] | 0 | 4.37 | 7 | 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 | 2.82 | 2 | 0 |
Pericardial Effusion Fluid accumulation within the PERICARDIUM. Serous effusions are associated with pericardial diseases. Hemopericardium is associated with trauma. Lipid-containing effusion (chylopericardium) results from leakage of THORACIC DUCT. Severe cases can lead to CARDIAC TAMPONADE. | 0 | 4.37 | 7 | 0 |
Malignant Melanoma [description not available] | 0 | 8.21 | 38 | 0 |
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 | 8.21 | 38 | 0 |
Abnormalities, Congenital, Nervous System [description not available] | 0 | 2.66 | 2 | 0 |
Edema-Proteinuria-Hypertension Gestosis [description not available] | 0 | 2.46 | 2 | 0 |
Edema, Pulmonary [description not available] | 0 | 3.62 | 9 | 0 |
Eclampsia Onset of HYPERREFLEXIA; SEIZURES; or COMA in a previously diagnosed pre-eclamptic patient (PRE-ECLAMPSIA). | 0 | 2.63 | 2 | 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 | 2.46 | 2 | 0 |
Pulmonary Edema Excessive accumulation of extravascular fluid in the lung, an indication of a serious underlying disease or disorder. Pulmonary edema prevents efficient PULMONARY GAS EXCHANGE in the PULMONARY ALVEOLI, and can be life-threatening. | 0 | 3.62 | 9 | 0 |
Constrictive Pericarditis [description not available] | 0 | 9.13 | 5 | 0 |
Infarct [description not available] | 0 | 6.74 | 21 | 1 |
Hepatocellular Carcinoma [description not available] | 0 | 13.46 | 114 | 11 |
Cancer of Liver [description not available] | 0 | 16.73 | 251 | 20 |
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 | 13.46 | 114 | 11 |
Liver Neoplasms Tumors or cancer of the LIVER. | 0 | 16.73 | 251 | 20 |
Angiofollicular Lymph Hyperplasia [description not available] | 0 | 2.41 | 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 | 2.41 | 1 | 0 |
Bradyarrhythmia [description not available] | 0 | 2.9 | 3 | 0 |
Abnormality, Heart [description not available] | 0 | 8.92 | 52 | 0 |
Symptom Cluster [description not available] | 0 | 10.94 | 37 | 1 |
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 | 2.9 | 3 | 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 | 8.92 | 52 | 0 |
Syndrome A characteristic symptom complex. | 0 | 10.94 | 37 | 1 |
Acute Anterior Wall Myocardial Infarction [description not available] | 0 | 5.77 | 6 | 1 |
Anterior Wall Myocardial Infarction MYOCARDIAL INFARCTION in which the anterior wall of the heart is involved. Anterior wall myocardial infarction is often caused by occlusion of the left anterior descending coronary artery. It can be categorized as anteroseptal or anterolateral wall myocardial infarction. | 0 | 5.77 | 6 | 1 |
Adrenocorticotropic Hormone, Inappropriate Secretion [description not available] | 0 | 3.33 | 1 | 0 |
Adenoma, Basal Cell [description not available] | 0 | 12.07 | 74 | 7 |
ACTH-Producing Pituitary Adenoma [description not available] | 0 | 3.51 | 2 | 0 |
Adenoma A benign epithelial tumor with a glandular organization. | 0 | 12.07 | 74 | 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 | 3.33 | 1 | 0 |
Adenitis, Salivary Gland [description not available] | 0 | 2.54 | 2 | 0 |
Chronic Kidney Diseases [description not available] | 0 | 10.84 | 38 | 2 |
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 | 10.84 | 38 | 2 |
Arthritides, Bacterial [description not available] | 0 | 4.17 | 6 | 0 |
Granulomatosis, Wegener's [description not available] | 0 | 2.97 | 4 | 0 |
Allergic Angiitis [description not available] | 0 | 2.49 | 2 | 0 |
Granulomatosis with Polyangiitis A multisystemic disease of a complex genetic background. It is characterized by inflammation of the blood vessels (VASCULITIS) leading to damage in any number of organs. The common features include granulomatous inflammation of the RESPIRATORY TRACT and KIDNEYS. Most patients have measurable autoantibodies (ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES) against MYELOBLASTIN. | 0 | 2.97 | 4 | 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 | 2.49 | 2 | 0 |
Acute Ischemic Stroke [description not available] | 0 | 5.01 | 10 | 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 | 10.01 | 10 | 0 |
Glaucoma, Angle Closure [description not available] | 0 | 2.31 | 1 | 0 |
Intraocular Pressure The pressure of the fluids in the eye. | 0 | 2.83 | 3 | 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 | 2.31 | 1 | 0 |
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 | 11.22 | 20 | 0 |
Brain Hemorrhage, Cerebral [description not available] | 0 | 6.38 | 27 | 0 |
Cerebral Ischemia [description not available] | 0 | 12.59 | 58 | 2 |
Hemorrhage, Subarachnoid [description not available] | 0 | 4.91 | 13 | 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 | 6.38 | 27 | 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 | 12.59 | 58 | 2 |
Subarachnoid Hemorrhage Bleeding into the intracranial or spinal SUBARACHNOID SPACE, most resulting from INTRACRANIAL ANEURYSM rupture. It can occur after traumatic injuries (SUBARACHNOID HEMORRHAGE, TRAUMATIC). Clinical features include HEADACHE; NAUSEA; VOMITING, nuchal rigidity, variable neurological deficits and reduced mental status. | 0 | 4.91 | 13 | 0 |
Dermatosclerosis [description not available] | 0 | 2.41 | 1 | 0 |
Dermatoses [description not available] | 0 | 12.43 | 92 | 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 | 2.41 | 1 | 0 |
Skin Diseases Diseases involving the DERMIS or EPIDERMIS. | 0 | 12.43 | 92 | 0 |
Anterior Optic Neuritis [description not available] | 0 | 6.83 | 23 | 1 |
Optic Neuritis Inflammation of the optic nerve. Commonly associated conditions include autoimmune disorders such as MULTIPLE SCLEROSIS, infections, and granulomatous diseases. Clinical features include retro-orbital pain that is aggravated by eye movement, loss of color vision, and contrast sensitivity that may progress to severe visual loss, an afferent pupillary defect (Marcus-Gunn pupil), and in some instances optic disc hyperemia and swelling. Inflammation may occur in the portion of the nerve within the globe (neuropapillitis or anterior optic neuritis) or the portion behind the globe (retrobulbar neuritis or posterior optic neuritis). | 0 | 6.83 | 23 | 1 |
Brain Inflammation [description not available] | 0 | 8.97 | 32 | 3 |
Encephalitis, Limbic [description not available] | 0 | 2.41 | 1 | 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 | 13.97 | 32 | 3 |
Hyponatremia Deficiency of sodium in the blood; salt depletion. (Dorland, 27th ed) | 0 | 3.06 | 4 | 0 |
Clinical Deterioration A critical disease progression, often measured by a set of clinical parameters, which activates HOSPITAL RAPID RESPONSE TEAM. | 0 | 2.41 | 1 | 0 |
Pulmonary Hypertension [description not available] | 0 | 5.44 | 13 | 0 |
Pulmonary Arterial Hypertension A progressive rare pulmonary disease characterized by high blood pressure in the PULMONARY ARTERY. | 0 | 7.76 | 2 | 0 |
Hypertension, Pulmonary Increased VASCULAR RESISTANCE in the PULMONARY CIRCULATION, usually secondary to HEART DISEASES or LUNG DISEASES. | 0 | 5.44 | 13 | 0 |
Carotid Artery Narrowing [description not available] | 0 | 11.16 | 45 | 6 |
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 | 16.16 | 45 | 6 |
Kidney Diseases Pathological processes of the KIDNEY or its component tissues. | 0 | 16.91 | 147 | 5 |
Cerebrospinal Fluid Drainage [description not available] | 0 | 6.69 | 17 | 0 |
Cerebrospinal Fluid Hypovolemia [description not available] | 0 | 8.66 | 42 | 1 |
Bone Cancer [description not available] | 0 | 10.75 | 65 | 1 |
Bone Neoplasms Tumors or cancer located in bone tissue or specific BONES. | 0 | 10.75 | 65 | 1 |
Lordosis The anterior concavity in the curvature of the lumbar and cervical spine as viewed from the side. The term usually refers to abnormally increased curvature (hollow back, saddle back, swayback). It does not include lordosis as normal mating posture in certain animals ( = POSTURE + SEX BEHAVIOR, ANIMAL). | 0 | 2.41 | 1 | 0 |
Female Genital Neoplasms [description not available] | 0 | 4.13 | 3 | 0 |
Genital Neoplasms, Female Tumor or cancer of the female reproductive tract (GENITALIA, FEMALE). | 0 | 4.13 | 3 | 0 |
Leukoencephalopathy Syndrome, Posterior [description not available] | 0 | 3.53 | 7 | 0 |
Abdominal Migraine [description not available] | 0 | 3.14 | 5 | 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 | 3.14 | 5 | 0 |
Blood Poisoning [description not available] | 0 | 4.2 | 16 | 0 |
Endotoxin Shock [description not available] | 0 | 3.51 | 8 | 0 |
Critical Illness A disease or state in which death is possible or imminent. | 0 | 2.96 | 3 | 0 |
Shock, Septic Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status. | 0 | 3.51 | 8 | 0 |
Sepsis Systemic inflammatory response syndrome with a proven or suspected infectious etiology. When sepsis is associated with organ dysfunction distant from the site of infection, it is called severe sepsis. When sepsis is accompanied by HYPOTENSION despite adequate fluid infusion, it is called SEPTIC SHOCK. | 0 | 4.2 | 16 | 0 |
Complication, Postoperative [description not available] | 0 | 12.02 | 61 | 3 |
Esophageal Fistula Abnormal passage communicating with the ESOPHAGUS. The most common type is TRACHEOESOPHAGEAL FISTULA between the esophagus and the TRACHEA. | 0 | 2.41 | 1 | 0 |
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 | 12.02 | 61 | 3 |
Brill-Symmers Disease [description not available] | 0 | 2.41 | 1 | 0 |
Neurolymphomatosis Infiltration of the nervous system by malignant lymphoma cells. | 0 | 2.41 | 1 | 0 |
Lymphoma, Follicular Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES. | 0 | 2.41 | 1 | 0 |
Injuries, Radiation [description not available] | 0 | 7.16 | 20 | 1 |
Necrosis The death of cells in an organ or tissue due to disease, injury or failure of the blood supply. | 0 | 11.92 | 103 | 3 |
IgG4 Related Systemic Disease [description not available] | 0 | 3.88 | 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 | 3.88 | 3 | 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 | 5.67 | 7 | 0 |
Angioma, Cavernous A tumor-like mass with large vascular space that is filled with blood or lymph. | 0 | 7.69 | 20 | 1 |
Tachyarrhythmia [description not available] | 0 | 8.56 | 8 | 0 |
Tachycardia Abnormally rapid heartbeat, usually with a HEART RATE above 100 beats per minute for adults. Tachycardia accompanied by disturbance in the cardiac depolarization (cardiac arrhythmia) is called tachyarrhythmia. | 0 | 3.56 | 8 | 0 |
Atrioventricular Conduction Block [description not available] | 0 | 3.31 | 5 | 0 |
Atrioventricular Block Impaired impulse conduction from HEART ATRIA to HEART VENTRICLES. AV block can mean delayed or completely blocked impulse conduction. | 0 | 3.31 | 5 | 0 |
Libman-Sacks Disease [description not available] | 0 | 8.02 | 11 | 1 |
Experimental Lung Inflammation Inflammation of any part, segment or lobe, of the lung parenchyma. | 0 | 4.45 | 8 | 0 |
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 | 8.02 | 11 | 1 |
Pneumonia Infection of the lung often accompanied by inflammation. | 0 | 4.45 | 8 | 0 |
Back Ache [description not available] | 0 | 6.18 | 12 | 1 |
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 | 5.91 | 17 | 0 |
Pott Disease [description not available] | 0 | 5.34 | 9 | 0 |
Back Pain Acute or chronic pain located in the posterior regions of the THORAX; LUMBOSACRAL REGION; or the adjacent regions. | 0 | 6.18 | 12 | 1 |
HbS Disease [description not available] | 0 | 5.65 | 16 | 1 |
Anemia, Cooley's [description not available] | 0 | 3.82 | 9 | 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 | 5.65 | 16 | 1 |
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 | 3.82 | 9 | 0 |
Iron Overload An excessive accumulation of iron in the body due to a greater than normal absorption of iron from the gastrointestinal tract or from parenteral injection. This may arise from idiopathic hemochromatosis, excessive iron intake, chronic alcoholism, certain types of refractory anemia, or transfusional hemosiderosis. (From Churchill's Illustrated Medical Dictionary, 1989) | 0 | 5.72 | 16 | 0 |
Death, Sudden The abrupt cessation of all vital bodily functions, manifested by the permanent loss of total cerebral, respiratory, and cardiovascular functions. | 0 | 5.46 | 3 | 1 |
Cranial Nerve II Injuries [description not available] | 0 | 2.41 | 1 | 0 |
Drop Attack [description not available] | 0 | 3.36 | 5 | 0 |
Syncope A transient loss of consciousness and postural tone caused by diminished blood flow to the brain (i.e., BRAIN ISCHEMIA). Presyncope refers to the sensation of lightheadedness and loss of strength that precedes a syncopal event or accompanies an incomplete syncope. (From Adams et al., Principles of Neurology, 6th ed, pp367-9) | 0 | 8.36 | 5 | 0 |
Canine Diseases [description not available] | 0 | 4.06 | 14 | 0 |
Disc, Herniated [description not available] | 0 | 11.35 | 48 | 3 |
Intervertebral Disc Displacement An INTERVERTEBRAL DISC in which the NUCLEUS PULPOSUS has protruded through surrounding ANNULUS FIBROSUS. This occurs most frequently in the lower lumbar region. | 0 | 11.35 | 48 | 3 |
Adverse Drug Event [description not available] | 0 | 17.47 | 43 | 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 | 12.47 | 43 | 1 |
Hyperglycemia, Postprandial Abnormally high BLOOD GLUCOSE level after a meal. | 0 | 4.12 | 5 | 0 |
Hyperglycemia Abnormally high BLOOD GLUCOSE level. | 0 | 4.12 | 5 | 0 |
Kidney Stones [description not available] | 0 | 9.35 | 4 | 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 | 4.35 | 4 | 0 |
Invasiveness, Neoplasm [description not available] | 0 | 12.78 | 92 | 5 |
Drug-Induced Cochlear Toxicity [description not available] | 0 | 2.6 | 1 | 0 |
Deaf Mutism [description not available] | 0 | 4.11 | 3 | 1 |
Ototoxicity Damage to the EAR or its function secondary to exposure to toxic substances such as drugs used in CHEMOTHERAPY; IMMUNOTHERAPY; or RADIATION. | 0 | 2.6 | 1 | 0 |
Deafness A general term for the complete loss of the ability to hear from both ears. | 0 | 4.11 | 3 | 1 |
Hypermobility, Joint [description not available] | 0 | 5.59 | 12 | 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 | 11.31 | 20 | 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 | 5.54 | 5 | 0 |
Acute Kidney Failure [description not available] | 0 | 10.87 | 47 | 1 |
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 | 10.87 | 47 | 1 |
Amyotonia Congenita [description not available] | 0 | 4.32 | 4 | 1 |
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 | 4.32 | 4 | 1 |
Acute Disseminated Encephalomyelitis [description not available] | 0 | 3.44 | 7 | 0 |
Clinically Isolated CNS Demyelinating Syndrome [description not available] | 0 | 9.62 | 29 | 4 |
Demyelinating Diseases Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system. | 0 | 9.62 | 29 | 4 |
Precordial Catch [description not available] | 0 | 7.54 | 27 | 1 |
Chest Pain Pressure, burning, or numbness in the chest. | 0 | 7.54 | 27 | 1 |
Brown-Sequard Disease [description not available] | 0 | 2.8 | 3 | 0 |
Anaplastic Astrocytoma [description not available] | 0 | 9.34 | 55 | 3 |
Absence Seizure [description not available] | 0 | 6.65 | 19 | 1 |
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 | 14.34 | 55 | 3 |
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 | 6.65 | 19 | 1 |
Cushing's Syndrome [description not available] | 0 | 5.08 | 6 | 0 |
Ache [description not available] | 0 | 9.85 | 39 | 2 |
Palsy [description not available] | 0 | 8.81 | 11 | 0 |
Amyotrophic Neuralgia [description not available] | 0 | 3.71 | 3 | 0 |
Cushing Syndrome A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent. | 0 | 5.08 | 6 | 0 |
Pain An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. | 0 | 9.85 | 39 | 2 |
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 | 3.81 | 11 | 0 |
Brachial Plexus Neuritis A syndrome associated with inflammation of the BRACHIAL PLEXUS. Clinical features include severe pain in the shoulder region which may be accompanied by MUSCLE WEAKNESS and loss of sensation in the upper extremity. This condition may be associated with VIRUS DISEASES; IMMUNIZATION; SURGERY; heroin use (see HEROIN DEPENDENCE); and other conditions. The term brachial neuralgia generally refers to pain associated with brachial plexus injury. (From Adams et al., Principles of Neurology, 6th ed, pp1355-6) | 0 | 3.71 | 3 | 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 | 6.41 | 8 | 2 |
Heart Valve Diseases Pathological conditions involving any of the various HEART VALVES and the associated structures (PAPILLARY MUSCLES and CHORDAE TENDINEAE). | 0 | 5.64 | 6 | 1 |
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 | 6.41 | 8 | 2 |
Coronary Artery Stenosis [description not available] | 0 | 11.63 | 18 | 1 |
Coronary Stenosis Narrowing or constriction of a coronary artery. | 0 | 11.63 | 18 | 1 |
Collagenous Fibroma [description not available] | 0 | 2.41 | 1 | 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 | 10.7 | 51 | 2 |
Cerebral Arteriosclerosis [description not available] | 0 | 8.4 | 14 | 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 | 8.4 | 14 | 0 |
Cancer of Prostate [description not available] | 0 | 10.64 | 86 | 2 |
Prostatic Neoplasms Tumors or cancer of the PROSTATE. | 0 | 10.64 | 86 | 2 |
Aortic Arteritis, Giant Cell [description not available] | 0 | 3.21 | 5 | 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 | 3.21 | 5 | 0 |
Convalescence The period of recovery following an illness. | 0 | 2.72 | 2 | 0 |
Cardiac Rupture, Traumatic [description not available] | 0 | 4.04 | 12 | 0 |
Granulomas [description not available] | 0 | 5.09 | 16 | 0 |
Granuloma A relatively small nodular inflammatory lesion containing grouped mononuclear phagocytes, caused by infectious and noninfectious agents. | 0 | 5.09 | 16 | 0 |
Cancer of Parotid [description not available] | 0 | 5.27 | 12 | 1 |
Parotid Neoplasms Tumors or cancer of the PAROTID GLAND. | 0 | 5.27 | 12 | 1 |
Corpus Luteum Cyst [description not available] | 0 | 2.74 | 3 | 0 |
Cancer of Ovary [description not available] | 0 | 6.64 | 35 | 0 |
Adnexal Torsion [description not available] | 0 | 7.41 | 1 | 0 |
Adnexal Diseases Diseases of the uterine appendages (ADNEXA UTERI) including diseases involving the OVARY, the FALLOPIAN TUBES, and ligaments of the uterus (BROAD LIGAMENT; ROUND LIGAMENT). | 0 | 3.6 | 2 | 0 |
Abnormality, Torsion [description not available] | 0 | 3.93 | 4 | 0 |
Ovarian Cysts General term for CYSTS and cystic diseases of the OVARY. | 0 | 2.74 | 3 | 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 | 6.64 | 35 | 0 |
Right Ventricular Dysfunction [description not available] | 0 | 9.36 | 18 | 0 |
Diffuse Parenchymal Lung Disease [description not available] | 0 | 2.74 | 3 | 0 |
Lung Diseases, Interstitial A diverse group of lung diseases that affect the lung parenchyma. They are characterized by an initial inflammation of PULMONARY ALVEOLI that extends to the interstitium and beyond leading to diffuse PULMONARY FIBROSIS. Interstitial lung diseases are classified by their etiology (known or unknown causes), and radiological-pathological features. | 0 | 2.74 | 3 | 0 |
Diffuse Mixed Small and Large Cell Lymphoma [description not available] | 0 | 3.81 | 11 | 0 |
Benign Supratentorial Neoplasms [description not available] | 0 | 5.91 | 13 | 2 |
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 | 3.81 | 11 | 0 |
Anaplastic Ependymoma [description not available] | 0 | 5.36 | 22 | 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 | 10.36 | 22 | 0 |
HIV Coinfection [description not available] | 0 | 5.42 | 13 | 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 | 5.42 | 13 | 0 |
Fusiform Aneurysm Elongated, spindle-shaped dilation in the wall of blood vessels, usually large ARTERIES with ATHEROSCLEROSIS. | 0 | 7.56 | 19 | 1 |
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 | 12.56 | 19 | 1 |
Cadaver A dead body, usually a human body. | 0 | 9.59 | 25 | 0 |
Glenoid Labral Tears [description not available] | 0 | 6.41 | 18 | 0 |
Rotator Cuff Injuries Injuries to the ROTATOR CUFF of the shoulder joint. | 0 | 6.41 | 18 | 0 |
Anti-Phospholipid Antibody Syndrome [description not available] | 0 | 7.82 | 6 | 4 |
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 | 12.82 | 6 | 4 |
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 | 3.36 | 6 | 0 |
Embolism, Pulmonary [description not available] | 0 | 12.85 | 45 | 6 |
Pulmonary Embolism Blocking of the PULMONARY ARTERY or one of its branches by an EMBOLUS. | 0 | 12.85 | 45 | 6 |
Breathlessness [description not available] | 0 | 3.95 | 12 | 0 |
Dyspnea Difficult or labored breathing. | 0 | 3.95 | 12 | 0 |
Anoxemia [description not available] | 0 | 4.57 | 24 | 0 |
Hypoxia Sub-optimal OXYGEN levels in the ambient air of living organisms. | 0 | 4.57 | 24 | 0 |
Atrial Remodeling Long-term changes in the electrophysiological parameters and/or anatomical structures of the HEART ATRIA that result from prolonged changes in atrial rate, often associated with ATRIAL FIBRILLATION or long periods of intense EXERCISE. | 0 | 6.83 | 12 | 0 |
Hospital-Acquired Condition [description not available] | 0 | 5.37 | 9 | 0 |
Acoustic Neuroma [description not available] | 0 | 11.95 | 94 | 3 |
Neonatal Death The death of a live-born INFANT less than 28 days of age. | 0 | 8.01 | 2 | 0 |
Delayed Effects, Prenatal Exposure [description not available] | 0 | 3.13 | 4 | 0 |
Infant, Small for Gestational Age An infant having a birth weight lower than expected for its gestational age. | 0 | 2.69 | 3 | 0 |
Bladder Cancer [description not available] | 0 | 7.81 | 23 | 1 |
Urinary Bladder Neoplasms Tumors or cancer of the URINARY BLADDER. | 0 | 7.81 | 23 | 1 |
Carcinoma, Transitional Cell A malignant neoplasm derived from TRANSITIONAL EPITHELIAL CELLS, occurring chiefly in the URINARY BLADDER; URETERS; or RENAL PELVIS. | 0 | 3.24 | 6 | 0 |
Metaplasia A condition in which there is a change of one adult cell type to another similar adult cell type. | 0 | 2.96 | 3 | 0 |
Cranial Nerve Diseases Disorders of one or more of the twelve cranial nerves. With the exception of the optic and olfactory nerves, this includes disorders of the brain stem nuclei from which the cranial nerves originate or terminate. | 0 | 5.54 | 16 | 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 | 5.5 | 15 | 0 |
Leukocytosis A transient increase in the number of leukocytes in a body fluid. | 0 | 4.47 | 4 | 0 |
Coronary Occlusion Complete blockage of blood flow through one of the CORONARY ARTERIES, usually from CORONARY ATHEROSCLEROSIS. | 0 | 3.43 | 6 | 0 |
Neuroleptic Malignant Syndrome A potentially fatal syndrome associated primarily with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS) which are in turn associated with dopaminergic receptor blockade (see RECEPTORS, DOPAMINE) in the BASAL GANGLIA and HYPOTHALAMUS, and sympathetic dysregulation. Clinical features include diffuse MUSCLE RIGIDITY; TREMOR; high FEVER; diaphoresis; labile blood pressure; cognitive dysfunction; and autonomic disturbances. Serum CPK level elevation and a leukocytosis may also be present. (From Adams et al., Principles of Neurology, 6th ed, p1199; Psychiatr Serv 1998 Sep;49(9):1163-72) | 0 | 2.41 | 1 | 0 |
alpha-Galactosidase A Deficiency [description not available] | 0 | 8.37 | 24 | 0 |
Fabry Disease An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders. | 0 | 8.37 | 24 | 0 |
Hip Injuries General or unspecified injuries involving the hip. | 0 | 3.92 | 4 | 0 |
Acute Respiratory Distress Syndrome [description not available] | 0 | 4.18 | 14 | 0 |
Acute Hypercapnic Respiratory Failure [description not available] | 0 | 4.02 | 11 | 0 |
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 | 4.18 | 14 | 0 |
Respiratory Insufficiency Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) | 0 | 4.02 | 11 | 0 |
Eisenmenger Syndrome [description not available] | 0 | 4.12 | 10 | 0 |
Eisenmenger Complex A condition associated with VENTRICULAR SEPTAL DEFECT and other congenital heart defects that allow the mixing of pulmonary and systemic circulation, increase blood flow into the lung, and subsequent responses to low oxygen in blood. This complex is characterized by progressive PULMONARY HYPERTENSION; HYPERTROPHY of the RIGHT VENTRICLE; CYANOSIS; and ERYTHROCYTOSIS. | 0 | 4.12 | 10 | 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 | 4.21 | 9 | 0 |
Cerebrovascular Moyamoya Disease [description not available] | 0 | 4.02 | 12 | 0 |
Cruveilhier-Baumgarten Syndrome Liver cirrhosis with intrahepatic portal obstruction, HYPERTENSION, and patent UMBILICAL VEINS. | 0 | 5.75 | 18 | 0 |
Hypertension, Portal Abnormal increase of resistance to blood flow within the hepatic PORTAL SYSTEM, frequently seen in LIVER CIRRHOSIS and conditions with obstruction of the PORTAL VEIN. | 0 | 5.75 | 18 | 0 |
Minimal Disease, Residual [description not available] | 0 | 7.87 | 37 | 0 |
Systolic Heart Failure [description not available] | 0 | 7.5 | 11 | 9 |
Heart Failure, Systolic Heart failure caused by abnormal myocardial contraction during SYSTOLE leading to defective cardiac emptying. | 0 | 7.5 | 11 | 9 |
Peripheral Nerve Diseases [description not available] | 0 | 6.03 | 25 | 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 | 6.03 | 25 | 0 |
Active Hyperemia [description not available] | 0 | 5.35 | 20 | 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 | 5.35 | 20 | 0 |
Rheumatoid Arthritis [description not available] | 0 | 10.38 | 44 | 6 |
Arthritis, Rheumatoid A chronic systemic disease, primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. Etiology is unknown, but autoimmune mechanisms have been implicated. | 0 | 10.38 | 44 | 6 |
Brain Swelling [description not available] | 0 | 8.27 | 36 | 1 |
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 | 8.27 | 36 | 1 |
Focal Nodular Hyperplasia Solitary or multiple benign hepatic vascular tumors, usually occurring in women of 20-50 years of age. The nodule, poorly encapsulated, consists of a central stellate fibrous scar and normal liver elements such as HEPATOCYTES, small BILE DUCTS, and KUPFFER CELLS among the intervening fibrous septa. The pale colored central scar represents large blood vessels with hyperplastic fibromuscular layer and narrowing lumen. | 0 | 6.65 | 11 | 1 |
Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted [description not available] | 0 | 3.57 | 5 | 0 |
Hepatitis C INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown. | 0 | 3.57 | 5 | 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 | 2.9 | 2 | 0 |
Prolapse The protrusion of an organ or part of an organ into a natural or artificial orifice. | 0 | 2.6 | 1 | 0 |
Break-Bone Fever [description not available] | 0 | 2.6 | 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 | 2.6 | 1 | 0 |
Hematoma A collection of blood outside the BLOOD VESSELS. Hematoma can be localized in an organ, space, or tissue. | 0 | 11.74 | 13 | 1 |
Acute Bacterial Prostatitis [description not available] | 0 | 5.03 | 3 | 1 |
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 | 10.03 | 3 | 1 |
Stillbirth The event that a FETUS is born dead or stillborn. | 0 | 3.55 | 2 | 0 |
Asystole [description not available] | 0 | 4.66 | 9 | 0 |
Heart Arrest Cessation of heart beat or MYOCARDIAL CONTRACTION. If it is treated within a few minutes, heart arrest can be reversed in most cases to normal cardiac rhythm and effective circulation. | 0 | 4.66 | 9 | 0 |
Deafness, Sudden Complete sensorineural hearing loss which develops suddenly over a period of hours or a few days. | 0 | 4.96 | 14 | 0 |
Adenohypophyseal Hyposecretion [description not available] | 0 | 3.9 | 4 | 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 | 3.88 | 4 | 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 | 3.9 | 4 | 0 |
Capillary Telangiectasia, Brain [description not available] | 0 | 5.46 | 14 | 0 |
Aneurysm, Arteriovenous [description not available] | 0 | 5.24 | 8 | 0 |
Diabetes Mellitus A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. | 0 | 4.78 | 10 | 0 |
Cirrhosis, Liver [description not available] | 0 | 7.76 | 58 | 0 |
Liver Cirrhosis Liver disease in which the normal microcirculation, the gross vascular anatomy, and the hepatic architecture have been variably destroyed and altered with fibrous septa surrounding regenerated or regenerating parenchymal nodules. | 0 | 7.76 | 58 | 0 |
Cardiac Death [description not available] | 0 | 2.51 | 2 | 0 |
Aneurysm, Thoracic Aortic [description not available] | 0 | 5.54 | 16 | 0 |
Experimental Spinal Cord Ischemia [description not available] | 0 | 2.6 | 1 | 0 |
Aortic Dissection [description not available] | 0 | 5.24 | 19 | 0 |
Aortic Aneurysm, Thoracic An abnormal balloon- or sac-like dilatation in the wall of the THORACIC AORTA. This proximal descending portion of aorta gives rise to the visceral and the parietal branches above the aortic hiatus at the diaphragm. | 0 | 5.54 | 16 | 0 |
Esophageal Squamous Cell Carcinoma A carcinoma that originates usually from cells on the surface of the middle and lower third of the ESOPHAGUS. Tumor cells exhibit typical squamous morphology and form large polypoid lesions. Mutations in RNF6, LZTS1, TGFBR2, DEC1, and WWOX1 genes are associated with this cancer. | 0 | 3.52 | 1 | 0 |
Ulcer A lesion on the surface of the skin or a mucous surface, produced by the sloughing of inflammatory necrotic tissue. | 0 | 2.6 | 1 | 0 |
Infections, Staphylococcal [description not available] | 0 | 6.02 | 19 | 0 |
Staphylococcal Infections Infections with bacteria of the genus STAPHYLOCOCCUS. | 0 | 6.02 | 19 | 0 |
Aortic Incompetence [description not available] | 0 | 4.35 | 5 | 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 | 4.35 | 5 | 0 |
Acute Lymphoid Leukemia [description not available] | 0 | 3.48 | 7 | 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 | 3.48 | 7 | 0 |
Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiency [description not available] | 0 | 2.6 | 1 | 0 |
Mucopolysaccharidosis III Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme. | 0 | 2.6 | 1 | 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 | 8.34 | 6 | 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 | 3.28 | 6 | 0 |
Adiadochokinesis [description not available] | 0 | 4.18 | 6 | 0 |
External Ophthalmoplegia [description not available] | 0 | 3.73 | 10 | 0 |
Cerebellar Ataxia Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90) | 0 | 9.18 | 6 | 0 |
Infectious Diseases [description not available] | 0 | 3.52 | 1 | 0 |
Angiitis, Central Nervous System [description not available] | 0 | 5 | 8 | 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 | 3.52 | 1 | 0 |
Dysautonomia [description not available] | 0 | 2.6 | 1 | 0 |
Sensation Disorders Disorders of the special senses (i.e., VISION; HEARING; TASTE; and SMELL) or somatosensory system (i.e., afferent components of the PERIPHERAL NERVOUS SYSTEM). | 0 | 2.75 | 3 | 0 |
Cardiac Papillary Fibroelastoma Primary tumors, predominantly of the CARDIAC VALVES, characterized by multiple papillary frond structures. Although histologically benign, they may result in complications (e.g., valve dysfunction, EMBOLISM; STROKE; and SUDDEN DEATH). | 0 | 2.6 | 1 | 0 |
Amyloid Deposits [description not available] | 0 | 5.48 | 14 | 0 |
Acute Confusional Senile Dementia [description not available] | 0 | 5.71 | 18 | 0 |
Alzheimer Disease A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57) | 0 | 5.71 | 18 | 0 |
Femoracetabular Impingement A pathological mechanical process that can lead to hip failure. It is caused by abnormalities of the ACETABULUM and/or FEMUR combined with rigorous hip motion, leading to repetitive collisions that damage the soft tissue structures. | 0 | 3.93 | 11 | 0 |
Fisher Syndrome [description not available] | 0 | 2.78 | 3 | 0 |
Facial Palsy [description not available] | 0 | 10.75 | 33 | 0 |
Dysesthesia [description not available] | 0 | 5.47 | 8 | 2 |
Bone Marrow Diseases Diseases involving the BONE MARROW. | 0 | 5.01 | 15 | 0 |
Cavernous Angioma, Central Nervous System [description not available] | 0 | 3.2 | 5 | 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 | 3.2 | 5 | 0 |
Arthritis, Juvenile Chronic [description not available] | 0 | 4.8 | 11 | 0 |
Temporomandibular Disorders [description not available] | 0 | 4.67 | 10 | 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 | 4.8 | 11 | 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 | 4.67 | 10 | 0 |
Dextro-Looped Transposition of the Great Arteries [description not available] | 0 | 5.3 | 7 | 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 | 5.3 | 7 | 0 |
Pancreatic Diseases Pathological processes of the PANCREAS. | 0 | 5.51 | 11 | 0 |
Chronic Kidney Failure [description not available] | 0 | 21.32 | 132 | 4 |
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 | 16.32 | 132 | 4 |
Nerve Pain [description not available] | 0 | 4.05 | 5 | 0 |
Neuralgia Intense or aching pain that occurs along the course or distribution of a peripheral or cranial nerve. | 0 | 4.05 | 5 | 0 |
Heatstroke [description not available] | 0 | 2.6 | 1 | 0 |
Heat Collapse [description not available] | 0 | 2.6 | 1 | 0 |
Heat Stroke A condition caused by the failure of body to dissipate heat in an excessively hot environment or during PHYSICAL EXERTION in a hot environment. Contrast to HEAT EXHAUSTION, the body temperature in heat stroke patient is dangerously high with red, hot skin accompanied by DELUSIONS; CONVULSIONS; or COMA. It can be a life-threatening emergency and is most common in infants and the elderly. | 0 | 2.6 | 1 | 0 |
Atypical Lipoma [description not available] | 0 | 5.54 | 16 | 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 | 5.54 | 16 | 0 |
EBV Infections [description not available] | 0 | 4.19 | 4 | 0 |
Duncan Disease [description not available] | 0 | 3.67 | 3 | 0 |
Lymphoproliferative Disorders Disorders characterized by proliferation of lymphoid tissue, general or unspecified. | 0 | 3.67 | 3 | 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 | 4.19 | 4 | 0 |
Ebstein Anomaly A congenital heart defect characterized by downward or apical displacement of the TRICUSPID VALVE, usually with the septal and posterior leaflets being attached to the wall of the RIGHT VENTRICLE. It is characterized by a huge RIGHT ATRIUM and a small and less effective right ventricle. | 0 | 2.69 | 2 | 0 |
Cardiomyopathy, Chagas [description not available] | 0 | 2.6 | 1 | 0 |
American Trypanosomiasis [description not available] | 0 | 2.98 | 4 | 0 |
Chagas Cardiomyopathy A disease of the CARDIAC MUSCLE developed subsequent to the initial protozoan infection by TRYPANOSOMA CRUZI. After infection, less than 10% develop acute illness such as MYOCARDITIS (mostly in children). The disease then enters a latent phase without clinical symptoms until about 20 years later. Myocardial symptoms of advanced CHAGAS DISEASE include conduction defects (HEART BLOCK) and CARDIOMEGALY. | 0 | 2.6 | 1 | 0 |
Chagas Disease Infection with the protozoan parasite TRYPANOSOMA CRUZI, a form of TRYPANOSOMIASIS endemic in Central and South America. It is named after the Brazilian physician Carlos Chagas, who discovered the parasite. Infection by the parasite (positive serologic result only) is distinguished from the clinical manifestations that develop years later, such as destruction of PARASYMPATHETIC GANGLIA; CHAGAS CARDIOMYOPATHY; and dysfunction of the ESOPHAGUS or COLON. | 0 | 2.98 | 4 | 0 |
Remission, Spontaneous A spontaneous diminution or abatement of a disease over time, without formal treatment. | 0 | 6.96 | 15 | 0 |
Aseptic Meningitis [description not available] | 0 | 4.38 | 4 | 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 | 4.38 | 4 | 0 |
Muscular Weakness [description not available] | 0 | 5.27 | 11 | 0 |
Spinal Stenosis Narrowing of the spinal canal. | 0 | 5.35 | 9 | 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 | 5.27 | 11 | 0 |
Embolus [description not available] | 0 | 3.75 | 3 | 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 | 3.75 | 3 | 0 |
Carcinoma, Anaplastic [description not available] | 0 | 11.12 | 63 | 4 |
Cancer of Oropharnyx [description not available] | 0 | 4.61 | 10 | 0 |
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 | 11.12 | 63 | 4 |
Oropharyngeal Neoplasms Tumors or cancer of the OROPHARYNX. | 0 | 4.61 | 10 | 0 |
Anterior Choroidal Artery Infarction [description not available] | 0 | 9.24 | 39 | 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 | 9.24 | 39 | 0 |
Acute Coronary Syndrome An episode of MYOCARDIAL ISCHEMIA that generally lasts longer than a transient anginal episode that ultimately may lead to MYOCARDIAL INFARCTION. | 0 | 8.13 | 16 | 0 |
Cholangiitis, Sclerosing [description not available] | 0 | 3.74 | 3 | 0 |
Cholangitis, Sclerosing Chronic inflammatory disease of the BILIARY TRACT. It is characterized by fibrosis and hardening of the intrahepatic and extrahepatic biliary ductal systems leading to bile duct strictures, CHOLESTASIS, and eventual BILIARY CIRRHOSIS. | 0 | 3.74 | 3 | 0 |
Chronic Hepatitis B [description not available] | 0 | 3.45 | 6 | 0 |
Acute Liver Injury, Drug-Induced [description not available] | 0 | 5.26 | 50 | 0 |
Chickungunya Fever [description not available] | 0 | 2.6 | 1 | 0 |
Cancer of Stomach [description not available] | 0 | 3.54 | 8 | 0 |
Acute Myelogenous Leukemia [description not available] | 0 | 2.72 | 3 | 0 |
Stomach Neoplasms Tumors or cancer of the STOMACH. | 0 | 3.54 | 8 | 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 | 2.72 | 3 | 0 |
Hepatitis B, Chronic INFLAMMATION of the LIVER in humans caused by HEPATITIS B VIRUS lasting six months or more. It is primarily transmitted by parenteral exposure, such as transfusion of contaminated blood or blood products, but can also be transmitted via sexual or intimate personal contact. | 0 | 3.45 | 6 | 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 | 5.26 | 50 | 0 |
Cerebral Microangiopathies [description not available] | 0 | 3.98 | 3 | 0 |
Cerebral Small Vessel Diseases Pathological processes or diseases where cerebral MICROVESSELS show abnormalities. They are often associated with aging, hypertension and risk factors for lacunar infarcts (see LACUNAR INFARCTION); LEUKOARAIOSIS; and CEREBRAL HEMORRHAGE. | 0 | 3.98 | 3 | 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 | 4.2 | 6 | 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 | 4.2 | 6 | 0 |
Aura [description not available] | 0 | 7.67 | 13 | 1 |
Diseases of Immune System [description not available] | 0 | 3.55 | 2 | 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 | 7.67 | 13 | 1 |
Immune System Diseases Disorders caused by abnormal or absent immunologic mechanisms, whether humoral, cell-mediated, or both. | 0 | 3.55 | 2 | 0 |
Non-ST-Elevation Myocardial Infarction [description not available] | 0 | 3.01 | 3 | 0 |
Non-ST Elevated Myocardial Infarction A myocardial infarction that does not produce elevations in the ST segments of the ELECTROCARDIOGRAM. ST segment elevation of the ECG is often used in determining the treatment protocol (see also ST Elevation Myocardial Infarction). | 0 | 3.01 | 3 | 0 |
Adenocarcinoma Of Kidney [description not available] | 0 | 10.9 | 28 | 4 |
Cancer of Kidney [description not available] | 0 | 11.92 | 51 | 4 |
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 | 10.9 | 28 | 4 |
Kidney Neoplasms Tumors or cancers of the KIDNEY. | 0 | 11.92 | 51 | 4 |
Blood Clot [description not available] | 0 | 10.42 | 43 | 2 |
Thrombosis Formation and development of a thrombus or blood clot in the blood vessel. | 0 | 15.42 | 43 | 2 |
Muscle Disorders [description not available] | 0 | 6.85 | 29 | 0 |
Muscular Diseases Acquired, familial, and congenital disorders of SKELETAL MUSCLE and SMOOTH MUSCLE. | 0 | 6.85 | 29 | 0 |
Airflow Obstruction, Chronic [description not available] | 0 | 6.67 | 9 | 0 |
Pulmonary Disease, Chronic Obstructive A disease of chronic diffuse irreversible airflow obstruction. Subcategories of COPD include CHRONIC BRONCHITIS and PULMONARY EMPHYSEMA. | 0 | 6.67 | 9 | 0 |
Chronic Illness [description not available] | 0 | 16.76 | 97 | 19 |
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 | 16.76 | 97 | 19 |
Sarcoma, Epithelioid [description not available] | 0 | 9 | 29 | 1 |
Sarcoma A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant. | 0 | 9 | 29 | 1 |
Encephalomyelitis, Inflammatory [description not available] | 0 | 3.92 | 4 | 0 |
Cerebromeningitis [description not available] | 0 | 4.79 | 7 | 0 |
Encephalomyelitis A general term indicating inflammation of the BRAIN and SPINAL CORD, often used to indicate an infectious process, but also applicable to a variety of autoimmune and toxic-metabolic conditions. There is significant overlap regarding the usage of this term and ENCEPHALITIS in the literature. | 0 | 3.92 | 4 | 0 |
Cranial Nerve V Diseases [description not available] | 0 | 4.2 | 6 | 0 |
ALS - Amyotrophic Lateral Sclerosis [description not available] | 0 | 2.79 | 3 | 0 |
Amyotrophic Lateral Sclerosis A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94) | 0 | 2.79 | 3 | 0 |
Autoimmune Disease [description not available] | 0 | 5.22 | 11 | 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 | 5.22 | 11 | 0 |
Cardiac Conduction Defect [description not available] | 0 | 2.63 | 2 | 0 |
Left Ventricular Outflow Obstruction [description not available] | 0 | 5.57 | 9 | 0 |
Acute Peripheral Vestibulopathy [description not available] | 0 | 2.9 | 3 | 0 |
Vestibular Neuronitis Idiopathic inflammation of the VESTIBULAR NERVE, characterized clinically by the acute or subacute onset of VERTIGO; NAUSEA; and imbalance. The COCHLEAR NERVE is typically spared and HEARING LOSS and TINNITUS do not usually occur. Symptoms usually resolve over a period of days to weeks. (Adams et al., Principles of Neurology, 6th ed, p304) | 0 | 2.9 | 3 | 0 |
Auricular Flutter [description not available] | 0 | 2.6 | 1 | 0 |
Atrial Flutter Rapid, irregular atrial contractions caused by a block of electrical impulse conduction in the right atrium and a reentrant wave front traveling up the inter-atrial septum and down the right atrial free wall or vice versa. Unlike ATRIAL FIBRILLATION which is caused by abnormal impulse generation, typical atrial flutter is caused by abnormal impulse conduction. As in atrial fibrillation, patients with atrial flutter cannot effectively pump blood into the lower chambers of the heart (HEART VENTRICLES). | 0 | 2.6 | 1 | 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 | 5.2 | 18 | 0 |
Auricular Syndrome of Ramsay Hunt [description not available] | 0 | 4.75 | 11 | 0 |
Cerebellar Dyssynergia [description not available] | 0 | 2.49 | 2 | 0 |
Cafe-au-Lait Spots with Pulmonic Stenosis [description not available] | 0 | 3.63 | 9 | 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 | 3.63 | 9 | 0 |
Alveolar Soft Part Sarcoma [description not available] | 0 | 8.52 | 1 | 0 |
Sarcoma, Alveolar Soft Part A variety of rare sarcoma having a reticulated fibrous stroma enclosing groups of sarcoma cells, which resemble epithelial cells and are enclosed in alveoli walled with connective tissue. It is a rare tumor, usually occurring between 15 and 35 years of age. It appears in the muscles of the extremities in adults and most commonly in the head and neck regions of children. Though slow-growing, it commonly metastasizes to the lungs, brain, bones, and lymph nodes. (DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1365) | 0 | 3.52 | 1 | 0 |
Pulmonary Arterial Remodeling [description not available] | 0 | 2.55 | 2 | 0 |
Extravasation of Contrast Media [description not available] | 0 | 8.05 | 31 | 0 |
Cancer of Colon [description not available] | 0 | 6.93 | 16 | 1 |
Colonic Neoplasms Tumors or cancer of the COLON. | 0 | 6.93 | 16 | 1 |
Diffuse Cutaneous Systemic Sclerosis [description not available] | 0 | 3.59 | 1 | 1 |
Scleroderma, Diffuse A rapid onset form of SYSTEMIC SCLERODERMA with progressive widespread SKIN thickening over the arms, the legs and the trunk, resulting in stiffness and disability. | 0 | 3.59 | 1 | 1 |
Cystadenocarcinoma, Serous A malignant cystic or semicystic neoplasm. It often occurs in the ovary and usually bilaterally. The external surface is usually covered with papillary excrescences. Microscopically, the papillary patterns are predominantly epithelial overgrowths with differentiated and undifferentiated papillary serous cystadenocarcinoma cells. Psammoma bodies may be present. The tumor generally adheres to surrounding structures and produces ascites. (From Hughes, Obstetric-Gynecologic Terminology, 1972, p185) | 0 | 2.21 | 1 | 0 |
Pain, Chronic [description not available] | 0 | 4.01 | 4 | 0 |
Chronic Pain Aching sensation that persists for more than a few months. It may or may not be associated with trauma or disease, and may persist after the initial injury has healed. Its localization, character, and timing are more vague than with acute pain. | 0 | 4.01 | 4 | 0 |
Fournier Disease [description not available] | 0 | 3.12 | 1 | 0 |
Complications of Diabetes Mellitus [description not available] | 0 | 5.49 | 5 | 0 |
Alcohol Abuse [description not available] | 0 | 3.67 | 3 | 0 |
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 | 3.67 | 3 | 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 | 4.48 | 8 | 0 |
Nasal Catarrh [description not available] | 0 | 3.65 | 3 | 0 |
Sinus Infections [description not available] | 0 | 4.46 | 8 | 0 |
Nasal Polyps Focal accumulations of EDEMA fluid in the NASAL MUCOSA accompanied by HYPERPLASIA of the associated submucosal connective tissue. Polyps may be NEOPLASMS, foci of INFLAMMATION, degenerative lesions, or malformations. | 0 | 2.73 | 3 | 0 |
Rhinitis Inflammation of the NASAL MUCOSA, the mucous membrane lining the NASAL CAVITIES. | 0 | 3.65 | 3 | 0 |
Sinusitis Inflammation of the NASAL MUCOSA in one or more of the PARANASAL SINUSES. | 0 | 9.46 | 8 | 0 |
Allergic Encephalomyelitis [description not available] | 0 | 10.33 | 13 | 0 |
Cancer of Head [description not available] | 0 | 10.67 | 45 | 3 |
Neoplasms, Skull Base [description not available] | 0 | 4.66 | 10 | 0 |
Benign Cranial Nerve Neoplasms [description not available] | 0 | 7.03 | 35 | 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 | 10.67 | 45 | 3 |
Koch's Disease [description not available] | 0 | 2.92 | 4 | 0 |
Tuberculosis Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM TUBERCULOSIS. | 0 | 2.92 | 4 | 0 |
Low Back Ache [description not available] | 0 | 5.35 | 13 | 1 |
Low Back Pain Acute or chronic pain in the lumbar or sacral regions, which may be associated with musculo-ligamentous SPRAINS AND STRAINS; INTERVERTEBRAL DISK DISPLACEMENT; and other conditions. | 0 | 5.35 | 13 | 1 |
Endocarditis, Loeffler [description not available] | 0 | 3.59 | 8 | 0 |
Tachycardia, Supraventricular A generic expression for any tachycardia that originates above the BUNDLE OF HIS. | 0 | 2.21 | 1 | 0 |
Hypereosinophilic Syndrome A heterogeneous group of disorders with the common feature of prolonged eosinophilia of unknown cause and associated organ system dysfunction, including the heart, central nervous system, kidneys, lungs, gastrointestinal tract, and skin. There is a massive increase in the number of EOSINOPHILS in the blood, mimicking leukemia, and extensive eosinophilic infiltration of the various organs. | 0 | 8.59 | 8 | 0 |
Bowel Diseases, Inflammatory [description not available] | 0 | 5.34 | 12 | 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 | 5.34 | 12 | 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 | 4.94 | 36 | 0 |
Colorectal Cancer [description not available] | 0 | 11.49 | 23 | 0 |
Colorectal Neoplasms Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI. | 0 | 6.49 | 23 | 0 |
Cancer of the Thyroid [description not available] | 0 | 3.91 | 4 | 0 |
Thyroid Neoplasms Tumors or cancer of the THYROID GLAND. | 0 | 3.91 | 4 | 0 |
Anal Fistula [description not available] | 0 | 5.87 | 8 | 1 |
B16 Melanoma [description not available] | 0 | 9.45 | 21 | 0 |
Depression Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders. | 0 | 4.34 | 4 | 1 |
Amyloid Angiopathy, Cerebral [description not available] | 0 | 2.98 | 4 | 0 |
Cerebral Amyloid Angiopathy A heterogeneous group of sporadic or familial disorders characterized by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES. Clinical features include multiple, small lobar CEREBRAL HEMORRHAGE; cerebral ischemia (BRAIN ISCHEMIA); and CEREBRAL INFARCTION. Cerebral amyloid angiopathy is unrelated to generalized AMYLOIDOSIS. Amyloidogenic peptides in this condition are nearly always the same ones found in ALZHEIMER DISEASE. (from Kumar: Robbins and Cotran: Pathologic Basis of Disease, 7th ed., 2005) | 0 | 2.98 | 4 | 0 |
Shoulder Injuries Injuries involving the SHOULDERS and SHOULDER JOINT. | 0 | 7.08 | 13 | 1 |
Cognitive Decline [description not available] | 0 | 3.99 | 4 | 0 |
Cognitive Dysfunction Diminished or impaired mental and/or intellectual function. | 0 | 3.99 | 4 | 0 |
Xanthoma [description not available] | 0 | 3.89 | 4 | 0 |
Hypophysitis Inflammation of the PITUITARY GLAND. | 0 | 3.17 | 1 | 0 |
Anti-PIT-1 Antibody Syndrome [description not available] | 0 | 3.17 | 1 | 0 |
Ventricular Dysfunction A condition in which HEART VENTRICLES exhibit impaired function. | 0 | 5 | 5 | 0 |
Lateral Sinus Thrombophlebitis [description not available] | 0 | 2.25 | 1 | 0 |
Carcinoma, Squamous Cell of Head and Neck [description not available] | 0 | 2.85 | 3 | 0 |
Carcinoma, Epidermoid [description not available] | 0 | 10.13 | 55 | 1 |
Squamous Cell Carcinoma of Head and Neck The most common type of head and neck carcinoma that originates from cells on the surface of the NASAL CAVITY; MOUTH; PARANASAL SINUSES, SALIVARY GLANDS, and LARYNX. Mutations in TNFRSF10B, PTEN, and ING1 genes are associated with this cancer. | 0 | 2.85 | 3 | 0 |
Carcinoma, Squamous Cell A carcinoma derived from stratified SQUAMOUS EPITHELIAL CELLS. It may also occur in sites where glandular or columnar epithelium is normally present. (From Stedman, 25th ed) | 0 | 10.13 | 55 | 1 |
Genetic Predisposition [description not available] | 0 | 6.68 | 7 | 1 |
Cardiac Edema [description not available] | 0 | 6.21 | 13 | 0 |
Edema, Cardiac Abnormal fluid retention by the body due to impaired cardiac function or heart failure. It is usually characterized by increase in venous and capillary pressure, and swollen legs when standing. It is different from the generalized edema caused by renal dysfunction (NEPHROTIC SYNDROME). | 0 | 6.21 | 13 | 0 |
Arthropathies [description not available] | 0 | 8.07 | 44 | 0 |
Joint Diseases Diseases involving the JOINTS. | 0 | 8.07 | 44 | 0 |
Apnea, Sleep [description not available] | 0 | 2.25 | 1 | 0 |
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 | 2.25 | 1 | 0 |
Arteriovenous Malformations, Cerebral [description not available] | 0 | 6.32 | 14 | 1 |
Intracranial Arteriovenous Malformations Congenital vascular anomalies in the brain characterized by direct communication between an artery and a vein without passing through the CAPILLARIES. The locations and size of the shunts determine the symptoms including HEADACHES; SEIZURES; STROKE; INTRACRANIAL HEMORRHAGES; mass effect; and vascular steal effect. | 0 | 11.32 | 14 | 1 |
Thromboembolism Obstruction of a blood vessel (embolism) by a blood clot (THROMBUS) in the blood stream. | 0 | 4.23 | 6 | 0 |
MELAS [description not available] | 0 | 3.17 | 1 | 0 |
MELAS Syndrome A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117) | 0 | 3.17 | 1 | 0 |
Enteritis Inflammation of any segment of the SMALL INTESTINE. | 0 | 2.54 | 2 | 0 |
Abdominal Aortic Aneurysm [description not available] | 0 | 6.84 | 24 | 1 |
Aortic Aneurysm, Ruptured [description not available] | 0 | 2.97 | 4 | 0 |
Aortic Aneurysm, Abdominal An abnormal balloon- or sac-like dilatation in the wall of the ABDOMINAL AORTA which gives rise to the visceral, the parietal, and the terminal (iliac) branches below the aortic hiatus at the diaphragm. | 0 | 6.84 | 24 | 1 |
Anterior Cerebral Circulation Infarction [description not available] | 0 | 5.74 | 4 | 1 |
Arterial Diseases, Carotid [description not available] | 0 | 9.24 | 23 | 1 |
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 | 9.24 | 23 | 1 |
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 | 5.74 | 4 | 1 |
6th Nerve Palsy [description not available] | 0 | 4.77 | 11 | 0 |
Hemorrhage, Retinal [description not available] | 0 | 2.31 | 1 | 0 |
Chondromalacia Softening and degeneration of the CARTILAGE. | 0 | 5.46 | 14 | 0 |
Cartilage Diseases Pathological processes involving the chondral tissue (CARTILAGE). | 0 | 5.46 | 14 | 0 |
Injury, Ischemia-Reperfusion [description not available] | 0 | 6.46 | 67 | 0 |
Reperfusion Injury Adverse functional, metabolic, or structural changes in tissues that result from the restoration of blood flow to the tissue (REPERFUSION) following ISCHEMIA. | 0 | 6.46 | 67 | 0 |
ER-Negative PR-Negative HER2-Negative Breast Cancer [description not available] | 0 | 3.46 | 6 | 0 |
Triple Negative Breast Neoplasms Breast neoplasms that do not express ESTROGEN RECEPTORS; PROGESTERONE RECEPTORS; and do not overexpress the NEU RECEPTOR/HER-2 PROTO-ONCOGENE PROTEIN. | 0 | 3.46 | 6 | 0 |
Cancer of the Retina [description not available] | 0 | 3.34 | 6 | 0 |
Eye Cancer, Retinoblastoma [description not available] | 0 | 3.81 | 11 | 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 | 3.81 | 11 | 0 |
Liver Dysfunction [description not available] | 0 | 12.97 | 106 | 7 |
Liver Diseases Pathological processes of the LIVER. | 0 | 12.97 | 106 | 7 |
Angiitis [description not available] | 0 | 4.59 | 9 | 0 |
Vasculitis Inflammation of any one of the blood vessels, including the ARTERIES; VEINS; and rest of the vasculature system in the body. | 0 | 4.59 | 9 | 0 |
Infections, Legionella pneumophila [description not available] | 0 | 2.63 | 2 | 0 |
Cancer of Eye [description not available] | 0 | 3.78 | 11 | 0 |
Asymptomatic Conditions [description not available] | 0 | 5.26 | 6 | 0 |
No-Reflow Phenomenon Markedly reduced or absent REPERFUSION in an infarct zone following the removal of an obstruction or constriction of an artery. | 0 | 2.25 | 1 | 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 | 9.63 | 10 | 0 |
Age-Related Osteoporosis [description not available] | 0 | 10.88 | 28 | 2 |
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 | 10.88 | 28 | 2 |
Electrocardiogram QT Prolonged [description not available] | 0 | 3.64 | 1 | 1 |
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 | 3.64 | 1 | 1 |
Encephalopathy, Toxic [description not available] | 0 | 4.24 | 6 | 0 |
Bilateral Headache [description not available] | 0 | 7.69 | 32 | 2 |
Hangman Fracture [description not available] | 0 | 4.65 | 10 | 0 |
Headache The symptom of PAIN in the cranial region. It may be an isolated benign occurrence or manifestation of a wide variety of HEADACHE DISORDERS. | 0 | 12.69 | 32 | 2 |
Spinal Fractures Broken bones in the vertebral column. | 0 | 4.65 | 10 | 0 |
Enterocolitis Inflammation of the MUCOSA of both the SMALL INTESTINE and the LARGE INTESTINE. Etiology includes ISCHEMIA, infections, allergic, and immune responses. | 0 | 2.25 | 1 | 0 |
Lymphatic Diseases Diseases of LYMPH; LYMPH NODES; or LYMPHATIC VESSELS. | 0 | 3.53 | 8 | 0 |
Ascites Accumulation or retention of free fluid within the peritoneal cavity. | 0 | 2.8 | 3 | 0 |
Addison Disease and Cerebral Sclerosis [description not available] | 0 | 3.3 | 6 | 0 |
Adrenoleukodystrophy An X-linked recessive disorder characterized by the accumulation of saturated very long chain fatty acids in the LYSOSOMES of ADRENAL CORTEX and the white matter of CENTRAL NERVOUS SYSTEM. This disease occurs almost exclusively in the males. Clinical features include the childhood onset of ATAXIA; NEUROBEHAVIORAL MANIFESTATIONS; HYPERPIGMENTATION; ADRENAL INSUFFICIENCY; SEIZURES; MUSCLE SPASTICITY; and DEMENTIA. The slowly progressive adult form is called adrenomyeloneuropathy. The defective gene ABCD1 is located at Xq28, and encodes the adrenoleukodystrophy protein (ATP-BINDING CASSETTE TRANSPORTERS). | 0 | 3.3 | 6 | 0 |
Pyogenic Sacroiliitis [description not available] | 0 | 3.23 | 5 | 0 |
Colitis Gravis [description not available] | 0 | 3.29 | 6 | 0 |
Colitis, Ulcerative Inflammation of the COLON that is predominantly confined to the MUCOSA. Its major symptoms include DIARRHEA, rectal BLEEDING, the passage of MUCUS, and ABDOMINAL PAIN. | 0 | 3.29 | 6 | 0 |
Infections, Coronavirus [description not available] | 0 | 3.86 | 3 | 0 |
Pneumonia, Viral Inflammation of the lung parenchyma that is caused by a viral infection. | 0 | 3.86 | 3 | 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 | 3.86 | 3 | 0 |
Brain Disorders [description not available] | 0 | 16.31 | 108 | 18 |
Bacterial Infections, Central Nervous System [description not available] | 0 | 2.25 | 1 | 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 | 16.31 | 108 | 18 |
Bayes Syndrome [description not available] | 0 | 2.59 | 2 | 0 |
Fibroid [description not available] | 0 | 5.61 | 12 | 0 |
Myofibroma A benign tumor that consists chiefly of fibrous CONNECTIVE TISSUE, with variable numbers of MUSCLE CELLS forming portions of the neoplasm (From Stedman's, 27th ed). | 0 | 2.25 | 1 | 0 |
Myofibromatosis A condition characterized by multiple formations of myofibromas (LEIOMYOMA). | 0 | 2.48 | 2 | 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 | 5.61 | 12 | 0 |
Cancer of Rectum [description not available] | 0 | 8.95 | 33 | 0 |
Rectal Neoplasms Tumors or cancer of the RECTUM. | 0 | 8.95 | 33 | 0 |
Ear Diseases Pathological processes of the ear, the hearing, and the equilibrium system of the body. | 0 | 4.34 | 7 | 0 |
Cerebral Infarction, Middle Cerebral Artery [description not available] | 0 | 4.69 | 10 | 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 | 4.69 | 10 | 0 |
Small Fiber Neuropathy Disorder of the peripheral nerves that primarily impair small nerve fibers. The affected small nerve fibers include myelinated A-delta fibers (see A FIBERS) and unmyelinated C FIBERS. Because these small fibers innervate skin and help control autonomic function, their neuropathy presents with neuropathic pain, reduced thermal and pain sensitivity, and autonomic dysfunction (e.g. abnormal sweating or facial flushing). Small fiber neuropathy can be idiopathic or associated with underlying diseases (e.g., AMYLOIDOSIS; DIABETES MELLITUS; SARCOIDOSIS; or VASCULITIS). | 0 | 7.25 | 1 | 0 |
Cranial Nerve III Diseases [description not available] | 0 | 4.57 | 9 | 0 |
Cavernous Sinus Thrombophlebitis [description not available] | 0 | 2.57 | 2 | 0 |
Corneal Dystrophies [description not available] | 0 | 2.25 | 1 | 0 |
Keratitis Inflammation of the cornea. | 0 | 2.25 | 1 | 0 |
Granulomatosis, Lymphomatoid [description not available] | 0 | 2.31 | 1 | 0 |
Acute Idiopathic Facial Neuropathy [description not available] | 0 | 4.21 | 6 | 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 | 9.21 | 6 | 0 |
Abdominal Epilepsy [description not available] | 0 | 3.12 | 5 | 0 |
Hamartoma A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area. | 0 | 9.82 | 12 | 0 |
Froehlich's Syndrome [description not available] | 0 | 2.43 | 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 | 3.12 | 5 | 0 |
Acrania [description not available] | 0 | 2.55 | 2 | 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 | 2.55 | 2 | 0 |
Cyst [description not available] | 0 | 7.65 | 48 | 0 |
Injury, Myocardial Reperfusion [description not available] | 0 | 7.09 | 31 | 0 |
EHS Tumor [description not available] | 0 | 2.9 | 4 | 0 |
Adenopathy [description not available] | 0 | 2.25 | 1 | 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 | 4.52 | 5 | 1 |
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 | 4.53 | 5 | 1 |
Peritoneal Carcinomatosis [description not available] | 0 | 5.58 | 10 | 0 |
Peritoneal Neoplasms Tumors or cancer of the PERITONEUM. | 0 | 5.58 | 10 | 0 |
Circulatory Collapse [description not available] | 0 | 2.77 | 3 | 0 |
Shock A pathological condition manifested by failure to perfuse or oxygenate vital organs. | 0 | 2.77 | 3 | 0 |
Carcinoma, Ductal, Pancreatic [description not available] | 0 | 5.32 | 4 | 1 |
Carcinoma, Pancreatic Ductal Carcinoma that arises from the PANCREATIC DUCTS. It accounts for the majority of cancers derived from the PANCREAS. | 0 | 5.32 | 4 | 1 |
Infections, Parvoviridae [description not available] | 0 | 2.57 | 2 | 0 |
Viral Diseases [description not available] | 0 | 3.74 | 3 | 0 |
Virus Diseases A general term for diseases caused by viruses. | 0 | 3.74 | 3 | 0 |
47,XX,+21 [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 | 2.25 | 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 | 3.43 | 7 | 0 |
Apnea, Obstructive Sleep [description not available] | 0 | 2.25 | 1 | 0 |
Sleep Apnea, Obstructive A disorder characterized by recurrent apneas during sleep despite persistent respiratory efforts. It is due to upper airway obstruction. The respiratory pauses may induce HYPERCAPNIA or HYPOXIA. Cardiac arrhythmias and elevation of systemic and pulmonary arterial pressures may occur. Frequent partial arousals occur throughout sleep, resulting in relative SLEEP DEPRIVATION and daytime tiredness. Associated conditions include OBESITY; ACROMEGALY; MYXEDEMA; micrognathia; MYOTONIC DYSTROPHY; adenotonsilar dystrophy; and NEUROMUSCULAR DISEASES. (From Adams et al., Principles of Neurology, 6th ed, p395) | 0 | 2.25 | 1 | 0 |
Idiopathic Inflammatory Myopathies [description not available] | 0 | 5.37 | 13 | 0 |
Myositis Inflammation of a muscle or muscle tissue. | 0 | 5.37 | 13 | 0 |
Angiogenesis, Pathologic [description not available] | 0 | 11.93 | 54 | 3 |
Impaired Glucose Tolerance [description not available] | 0 | 2.25 | 1 | 0 |
Glucose Intolerance A pathological state in which BLOOD GLUCOSE level is less than approximately 140 mg/100 ml of PLASMA at fasting, and above approximately 200 mg/100 ml plasma at 30-, 60-, or 90-minute during a GLUCOSE TOLERANCE TEST. This condition is seen frequently in DIABETES MELLITUS, but also occurs with other diseases and MALNUTRITION. | 0 | 2.25 | 1 | 0 |
Coronary Vessel Anomalies Malformations of CORONARY VESSELS, either arteries or veins. Included are anomalous origins of coronary arteries; ARTERIOVENOUS FISTULA; CORONARY ANEURYSM; MYOCARDIAL BRIDGING; and others. | 0 | 2.98 | 4 | 0 |
Acquired Facial Neuropathy [description not available] | 0 | 4.87 | 13 | 0 |
Hyperthermia An abnormal elevation of body temperature, usually as a result of inability to regulate core body temperature due to non-pathologic factors. | 0 | 7.25 | 1 | 0 |
Emesis [description not available] | 0 | 4.51 | 5 | 1 |
Vomiting The forcible expulsion of the contents of the STOMACH through the MOUTH. | 0 | 4.51 | 5 | 1 |
Deafness, Transitory [description not available] | 0 | 5.29 | 7 | 0 |
Hearing Loss A general term for the complete or partial loss of the ability to hear from one or both ears. | 0 | 5.29 | 7 | 0 |
Cryptogenic Fibrosing Alveolitis [description not available] | 0 | 2.25 | 1 | 0 |
Centriacinar Emphysema [description not available] | 0 | 2.57 | 2 | 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 | 2.25 | 1 | 0 |
Lymph Node Metastasis [description not available] | 0 | 13.81 | 69 | 3 |
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 | 2.49 | 2 | 0 |
Familial Waldenstrom's Macroglobulinaemia [description not available] | 0 | 2.25 | 1 | 0 |
Cauda Equina Syndrome Compressive lesion affecting the nerve roots of the CAUDA EQUINA (e.g., compression, herniation, inflammation, rupture, or stenosis), which controls the function of the bladder and bowel. Symptoms may include neurological dysfunction of bladder or bowels, loss of sexual sensation and altered sensation or paralysis in the lower extremities. | 0 | 2.25 | 1 | 0 |
Waldenstrom Macroglobulinemia A lymphoproliferative disorder characterized by pleomorphic B-LYMPHOCYTES including PLASMA CELLS, with increased levels of monoclonal serum IMMUNOGLOBULIN M. There is lymphoplasmacytic cells infiltration into bone marrow and often other tissues, also known as lymphoplasmacytic lymphoma. Clinical features include ANEMIA; HEMORRHAGES; and hyperviscosity. | 0 | 2.25 | 1 | 0 |
Hematologic Malignancies [description not available] | 0 | 2.49 | 2 | 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 | 2.49 | 2 | 0 |
Food Poisoning [description not available] | 0 | 2.31 | 1 | 0 |
Isolated Non-compaction of the Ventricular Myocardium [description not available] | 0 | 11.77 | 12 | 1 |
Germinoblastoma [description not available] | 0 | 9.18 | 25 | 3 |
Central Nervous System Neoplasm [description not available] | 0 | 8.06 | 20 | 1 |
Lymphoma A general term for various neoplastic diseases of the lymphoid tissue. | 0 | 14.18 | 25 | 3 |
Central Nervous System Neoplasms Benign and malignant neoplastic processes that arise from or secondarily involve the brain, spinal cord, or meninges. | 0 | 8.06 | 20 | 1 |
Hypertension, Essential [description not available] | 0 | 2.31 | 1 | 0 |
Essential Hypertension Hypertension that occurs without known cause, or preexisting renal disease. Associated polymorphisms for a number of genes have been identified, including AGT, GNB3, and ECE1. OMIM: 145500 | 0 | 2.31 | 1 | 0 |
Distal Muscular Dystrophies [description not available] | 0 | 2.31 | 1 | 0 |
Atrophy, Muscle [description not available] | 0 | 2.99 | 4 | 0 |
Muscular Atrophy Derangement in size and number of muscle fibers occurring with aging, reduction in blood supply, or following immobilization, prolonged weightlessness, malnutrition, and particularly in denervation. | 0 | 2.99 | 4 | 0 |
Distal Myopathies A heterogeneous group of genetic disorders characterized by progressive MUSCULAR ATROPHY and MUSCLE WEAKNESS beginning in the hands, the legs, or the feet. Most are adult-onset autosomal dominant forms. Others are autosomal recessive. | 0 | 2.31 | 1 | 0 |
Brain Stem Neoplasms, Primary [description not available] | 0 | 3.45 | 7 | 0 |
DIPG Brain Tumors [description not available] | 0 | 2.31 | 1 | 0 |
Diffuse Intrinsic Pontine Glioma A rare, aggressive brain tumor that forms in the GLIAL CELLS in the PONS. | 0 | 2.31 | 1 | 0 |
Brain Stem Neoplasms Benign and malignant intra-axial tumors of the MESENCEPHALON; PONS; or MEDULLA OBLONGATA of the BRAIN STEM. Primary and metastatic neoplasms may occur in this location. Clinical features include ATAXIA, cranial neuropathies (see CRANIAL NERVE DISEASES), NAUSEA, hemiparesis (see HEMIPLEGIA), and quadriparesis. Primary brain stem neoplasms are more frequent in children. Histologic subtypes include GLIOMA; HEMANGIOBLASTOMA; GANGLIOGLIOMA; and EPENDYMOMA. | 0 | 3.45 | 7 | 0 |
Injuries Used with anatomic headings, animals, and sports for wounds and injuries. Excludes cell damage, for which pathology is used. | 0 | 3.8 | 11 | 0 |
Wounds and Injuries Damage inflicted on the body as the direct or indirect result of an external force, with or without disruption of structural continuity. | 0 | 3.8 | 11 | 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 | 11.21 | 52 | 3 |
Renal Artery Stenosis [description not available] | 0 | 11.61 | 70 | 6 |
Renal Artery Obstruction Narrowing or occlusion of the RENAL ARTERY or arteries. It is due usually to ATHEROSCLEROSIS; FIBROMUSCULAR DYSPLASIA; THROMBOSIS; EMBOLISM, or external pressure. The reduced renal perfusion can lead to renovascular hypertension (HYPERTENSION, RENOVASCULAR). | 0 | 11.61 | 70 | 6 |
Alloxan Diabetes [description not available] | 0 | 4.1 | 15 | 0 |
Aseptic Necrosis of Bone [description not available] | 0 | 7.97 | 11 | 1 |
Osteonecrosis Death of a bone or part of a bone, either atraumatic or posttraumatic. | 0 | 7.97 | 11 | 1 |
Hyperthyroid [description not available] | 0 | 2.95 | 4 | 0 |
Hyperthyroidism Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE. | 0 | 2.95 | 4 | 0 |
Thyroid Cancer, Anaplastic [description not available] | 0 | 2.31 | 1 | 0 |
Thyroid Carcinoma, Anaplastic An aggressive THYROID GLAND malignancy which generally occurs in IODINE-deficient areas in people with previous thyroid pathology such as GOITER. It is associated with CELL DEDIFFERENTIATION of THYROID CARCINOMA (e.g., FOLLICULAR THYROID CARCINOMA; PAPILLARY THYROID CANCER). Typical initial presentation is a rapidly growing neck mass which upon metastasis is associated with DYSPHAGIA; NECK PAIN; bone pain; DYSPNEA; and NEUROLOGIC DEFICITS. | 0 | 2.31 | 1 | 0 |
Fatty Liver, Nonalcoholic [description not available] | 0 | 2.8 | 3 | 0 |
Non-alcoholic Fatty Liver Disease Fatty liver finding without excessive ALCOHOL CONSUMPTION. | 0 | 2.8 | 3 | 0 |
Pulmonary Sarcoidosis [description not available] | 0 | 8.18 | 5 | 0 |
Sarcoidosis, Pulmonary Sarcoidosis affecting predominantly the lungs, the site most frequently involved and most commonly causing morbidity and mortality in sarcoidosis. Pulmonary sarcoidosis is characterized by sharply circumscribed granulomas in the alveolar, bronchial, and vascular walls, composed of tightly packed cells derived from the mononuclear phagocyte system. The clinical symptoms when present are dyspnea upon exertion, nonproductive cough, and wheezing. (Cecil Textbook of Medicine, 19th ed, p431) | 0 | 3.18 | 5 | 0 |
Aneurysm, Coronary [description not available] | 0 | 4.23 | 6 | 0 |
Burns Injuries to tissues caused by contact with heat, steam, chemicals (BURNS, CHEMICAL), electricity (BURNS, ELECTRIC), or the like. | 0 | 2.47 | 2 | 0 |
Anaphylactic Reaction [description not available] | 0 | 9.04 | 34 | 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 | 7.25 | 1 | 0 |
Allergic Acute Coronary Syndrome [description not available] | 0 | 2.25 | 1 | 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 | 9.04 | 34 | 0 |
Neurilemoma [description not available] | 0 | 6.76 | 41 | 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 | 6.76 | 41 | 0 |
Hepatic Insufficiency Conditions in which the LIVER functions fall below the normal ranges. Severe hepatic insufficiency may cause LIVER FAILURE or DEATH. Treatment may include LIVER TRANSPLANTATION. | 0 | 2.41 | 1 | 0 |
Hepatic Failure [description not available] | 0 | 4.05 | 5 | 0 |
Liver Failure Severe inability of the LIVER to perform its normal metabolic functions, as evidenced by severe JAUNDICE and abnormal serum levels of AMMONIA; BILIRUBIN; ALKALINE PHOSPHATASE; ASPARTATE AMINOTRANSFERASE; LACTATE DEHYDROGENASES; and albumin/globulin ratio. (Blakiston's Gould Medical Dictionary, 4th ed) | 0 | 4.05 | 5 | 0 |
Carbon Monoxide Poisoning Toxic asphyxiation due to the displacement of oxygen from oxyhemoglobin by carbon monoxide. | 0 | 3.23 | 1 | 0 |
Angioblastic Meningioma [description not available] | 0 | 9.77 | 90 | 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 | 9.77 | 90 | 1 |
Limb-Girdle Muscular Dystrophies [description not available] | 0 | 2.31 | 1 | 0 |
Muscular Dystrophies, Limb-Girdle A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles). | 0 | 2.31 | 1 | 0 |
Aqueductal Stenosis [description not available] | 0 | 4.28 | 18 | 0 |
Adenoma, Prolactin-Secreting, Pituitary [description not available] | 0 | 7.46 | 18 | 3 |
Abnormalities, Cardiovascular [description not available] | 0 | 2.49 | 2 | 0 |
Cardiovascular Abnormalities Congenital, inherited, or acquired anomalies of the CARDIOVASCULAR SYSTEM, including the HEART and BLOOD VESSELS. | 0 | 2.49 | 2 | 0 |
HPV Infection [description not available] | 0 | 2.41 | 1 | 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 | 2.41 | 1 | 0 |
Bone Diseases Diseases of BONES. | 0 | 6.2 | 18 | 0 |
B-Cell Chronic Lymphocytic Leukemia [description not available] | 0 | 2.31 | 1 | 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 | 2.31 | 1 | 0 |
Astroblastoma [description not available] | 0 | 3.29 | 6 | 0 |
Neoplasms, Neuroepithelial Neoplasms composed of neuroepithelial cells, which have the capacity to differentiate into NEURONS, oligodendrocytes, and ASTROCYTES. The majority of craniospinal tumors are of neuroepithelial origin. (From Dev Biol 1998 Aug 1;200(1):1-5) | 0 | 3.29 | 6 | 0 |
AIDS Seroconversion [description not available] | 0 | 5.26 | 6 | 0 |
Genetic Diseases [description not available] | 0 | 2.31 | 1 | 0 |
A-V Dissociation [description not available] | 0 | 2.58 | 2 | 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 | 2.31 | 1 | 0 |
Preterm Birth [description not available] | 0 | 2.31 | 1 | 0 |
Diastolic Heart Failure [description not available] | 0 | 2.31 | 1 | 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 | 2.31 | 1 | 0 |
Heart Failure, Diastolic Heart failure caused by abnormal myocardial relaxation during DIASTOLE leading to defective cardiac filling. | 0 | 2.31 | 1 | 0 |
Injuries, Wrist [description not available] | 0 | 2.99 | 4 | 0 |
Abnormalities, Multiple Congenital abnormalities that affect more than one organ or body structure. | 0 | 2.31 | 1 | 0 |
Dwarfism, Growth Hormone Deficiency [description not available] | 0 | 2.31 | 1 | 0 |
Central Hypothyroidism [description not available] | 0 | 2.57 | 2 | 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 | 2.31 | 1 | 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 | 2.57 | 2 | 0 |
Androgen-Independent Prostatic Cancer [description not available] | 0 | 2.15 | 1 | 0 |
Prostatic Neoplasms, Castration-Resistant Tumors or cancer of the PROSTATE which can grow in the presence of low or residual amount of androgen hormones such as TESTOSTERONE. | 0 | 2.15 | 1 | 0 |
Leukoaraiosis Non-specific white matter changes in the BRAIN, often seen after age 65. Changes include loss of AXONS; MYELIN pallor, GLIOSIS, loss of ependymal cells, and enlarged perivascular spaces. Leukoaraiosis is a risk factor for DEMENTIA and CEREBROVASCULAR DISORDERS. | 0 | 2.52 | 2 | 0 |
Placenta Increta Invasion of CHORIONIC VILLI occurs deep into the MYOMETRIUM. | 0 | 3.91 | 4 | 0 |
Placenta Praevia [description not available] | 0 | 3.75 | 3 | 0 |
Placenta Accreta Abnormal placentation in which all or parts of the PLACENTA are attached directly to the MYOMETRIUM due to a complete or partial absence of DECIDUA. It is associated with POSTPARTUM HEMORRHAGE because of the failure of placental separation. | 0 | 8.91 | 4 | 0 |
Placenta Previa Abnormal placentation in which the PLACENTA implants in the lower segment of the UTERUS (the zone of dilation) and may cover part or all of the opening of the CERVIX. It is often associated with serious antepartum bleeding and PREMATURE LABOR. | 0 | 3.75 | 3 | 0 |
Focal Clonic Seizures [description not available] | 0 | 2.15 | 1 | 0 |
Drug Refractory Epilepsy [description not available] | 0 | 2.15 | 1 | 0 |
Benign Psychomotor Epilepsy, Childhood [description not available] | 0 | 4.81 | 7 | 1 |
Altidudinal Hemianopia [description not available] | 0 | 2.15 | 1 | 0 |
Complex Partial Epilepsy [description not available] | 0 | 3.26 | 6 | 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 | 4.81 | 7 | 1 |
Epilepsy, Complex Partial A disorder characterized by recurrent partial seizures marked by impairment of cognition. During the seizure the individual may experience a wide variety of psychic phenomenon including formed hallucinations, illusions, deja vu, intense emotional feelings, confusion, and spatial disorientation. Focal motor activity, sensory alterations and AUTOMATISM may also occur. Complex partial seizures often originate from foci in one or both temporal lobes. The etiology may be idiopathic (cryptogenic partial complex epilepsy) or occur as a secondary manifestation of a focal cortical lesion (symptomatic partial complex epilepsy). (From Adams et al., Principles of Neurology, 6th ed, pp317-8) | 0 | 3.26 | 6 | 0 |
Epilepsy, Partial, Motor A disorder characterized by recurrent localized paroxysmal discharges of cerebral neurons that give rise to seizures that have motor manifestations. The majority of partial motor seizures originate in the FRONTAL LOBE (see also EPILEPSY, FRONTAL LOBE). Motor seizures may manifest as tonic or clonic movements involving the face, one limb or one side of the body. A variety of more complex patterns of movement, including abnormal posturing of extremities, may also occur. | 0 | 2.15 | 1 | 0 |
Coxarthrosis [description not available] | 0 | 4.49 | 8 | 0 |
Osteoarthritis, Hip Noninflammatory degenerative disease of the hip joint which usually appears in late middle or old age. It is characterized by growth or maturational disturbances in the femoral neck and head, as well as acetabular dysplasia. A dominant symptom is pain on weight-bearing or motion. | 0 | 4.49 | 8 | 0 |
Brain Hemorrhage [description not available] | 0 | 4.14 | 3 | 1 |
Intracranial Hemorrhages Bleeding within the SKULL, including hemorrhages in the brain and the three membranes of MENINGES. The escape of blood often leads to the formation of HEMATOMA in the cranial epidural, subdural, and subarachnoid spaces. | 0 | 4.14 | 3 | 1 |
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 | 3.62 | 9 | 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 | 6.19 | 12 | 1 |
Ambulation Disorders, Neurologic [description not available] | 0 | 5.61 | 6 | 1 |
Colonic Inertia Symptom characterized by the passage of stool once a week or less. | 0 | 3.5 | 2 | 0 |
Dilatation, Pathologic The condition of an anatomical structure's being dilated beyond normal dimensions. | 0 | 4.44 | 8 | 0 |
Conus Medullaris Syndrome [description not available] | 0 | 6.27 | 19 | 0 |
Urination Disorders Abnormalities in the process of URINE voiding, including bladder control, frequency of URINATION, as well as the volume and composition of URINE. | 0 | 3.47 | 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 | 8.5 | 2 | 0 |
Deep Vein Thrombosis [description not available] | 0 | 9.24 | 29 | 1 |
Venous Thrombosis The formation or presence of a blood clot (THROMBUS) within a vein. | 0 | 9.24 | 29 | 1 |
Alveolitis, Fibrosing [description not available] | 0 | 3.3 | 6 | 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 | 8.3 | 6 | 0 |
Congenital Familial Lymphedema [description not available] | 0 | 4.76 | 11 | 0 |
Lymphedema Edema due to obstruction of lymph vessels or disorders of the lymph nodes. | 0 | 9.76 | 11 | 0 |
Choroid Plexus Papilloma [description not available] | 0 | 4.79 | 2 | 1 |
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 | 2.15 | 1 | 0 |
Neoplasms, Skull [description not available] | 0 | 6.47 | 24 | 0 |
Erythema Nodosum An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral. These nodules are located predominantly on the shins with less common occurrence on the thighs and forearms. They undergo characteristic color changes ending in temporary bruise-like areas. This condition usually subsides in 3-6 weeks without scarring or atrophy. | 0 | 2.49 | 2 | 0 |
Benign Infratentorial Neoplasms [description not available] | 0 | 2.43 | 2 | 0 |
Joint Loose Bodies Fibrous, bony, cartilaginous and osteocartilaginous fragments in a synovial joint. Major causes are osteochondritis dissecans, synovial chondromatosis, osteophytes, fractured articular surfaces and damaged menisci. | 0 | 4.51 | 5 | 0 |
Lung Injury, Acute [description not available] | 0 | 2.52 | 2 | 0 |
Acute Edematous Pancreatitis [description not available] | 0 | 6.62 | 19 | 1 |
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 | 6.62 | 19 | 1 |
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). | 0 | 7.52 | 2 | 0 |
Cancer-Associated Pain [description not available] | 0 | 2.15 | 1 | 0 |
Cancer Pain Pain that may be caused by or related to cellular, tissue, and systemic changes that occur during NEOPLASM growth, tissue invasion, and METASTASIS. | 0 | 2.15 | 1 | 0 |
Spinal Neoplasms New abnormal growth of tissue in the SPINE. | 0 | 9.95 | 43 | 3 |
Claustrophobia [description not available] | 0 | 3.66 | 3 | 0 |
Anxiety Feelings or emotions of dread, apprehension, and impending disaster but not disabling as with ANXIETY DISORDERS. | 0 | 3.63 | 3 | 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 | 3.66 | 3 | 0 |
Phlebitis, Sagittal Sinus, Septic [description not available] | 0 | 2.17 | 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 | 2.49 | 2 | 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 | 2.17 | 1 | 0 |
Prediabetes [description not available] | 0 | 2.17 | 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 | 2.17 | 1 | 0 |
Spinal Diseases Diseases involving the SPINE. | 0 | 16.38 | 46 | 3 |
Complications, Pregnancy [description not available] | 0 | 11.47 | 28 | 0 |
Aural Cholesteatoma [description not available] | 0 | 5.84 | 8 | 1 |
Basedow Disease [description not available] | 0 | 2.7 | 3 | 0 |
Autoimmune Thyroiditis [description not available] | 0 | 2.17 | 1 | 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 | 2.7 | 3 | 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 | 2.17 | 1 | 0 |
Cerebral Malaria [description not available] | 0 | 3.5 | 2 | 0 |
Condition, Preneoplastic [description not available] | 0 | 2.17 | 1 | 0 |
Precancerous Conditions Pathological conditions that tend eventually to become malignant. | 0 | 2.17 | 1 | 0 |
Liver Steatosis [description not available] | 0 | 5.66 | 18 | 0 |
Fatty Liver Lipid infiltration of the hepatic parenchymal cells resulting in a yellow-colored liver. The abnormal lipid accumulation is usually in the form of TRIGLYCERIDES, either as a single large droplet or multiple small droplets. Fatty liver is caused by an imbalance in the metabolism of FATTY ACIDS. | 0 | 5.66 | 18 | 0 |
Brain Hemorrhage, Cerebral, Traumatic [description not available] | 0 | 2.48 | 2 | 0 |
Acoustic Nerve Diseases [description not available] | 0 | 3.42 | 7 | 0 |
Acute Generalised Exanthematous Pustulosis [description not available] | 0 | 2.17 | 1 | 0 |
Cancer of Skin [description not available] | 0 | 5.32 | 21 | 0 |
Skin Neoplasms Tumors or cancer of the SKIN. | 0 | 5.32 | 21 | 0 |
Anemias, Iron-Deficiency [description not available] | 0 | 2.17 | 1 | 0 |
Lipomatosis A disorder characterized by the accumulation of encapsulated or unencapsulated tumor-like fatty tissue resembling LIPOMA. | 0 | 2.95 | 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 | 2.17 | 1 | 0 |
Foot Diseases Anatomical and functional disorders affecting the foot. | 0 | 5.34 | 7 | 2 |
Equine Diseases [description not available] | 0 | 5.12 | 3 | 1 |
Gait Disorders, Animal [description not available] | 0 | 3.56 | 1 | 1 |
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 | 2.17 | 1 | 0 |
Anton Syndrome [description not available] | 0 | 2.17 | 1 | 0 |
Adhesions, Tissue [description not available] | 0 | 2.72 | 3 | 0 |
Endoleak Postoperative hemorrhage from an endovascular AORTIC ANEURYSM repaired with endoluminal placement of stent grafts (BLOOD VESSEL PROSTHESIS IMPLANTATION). It is associated with pressurization, expansion, and eventual rupture of the aneurysm. | 0 | 2.78 | 3 | 0 |
Seroma Tumor-like sterile accumulation of serum in a tissue, organ, or cavity. It results from a tissue insult and is the product of tissue inflammation. It most commonly occurs following MASTECTOMY. | 0 | 2.17 | 1 | 0 |
Brain Dead [description not available] | 0 | 2.53 | 2 | 0 |
Angina at Rest [description not available] | 0 | 2.97 | 4 | 0 |
Angina, Unstable Precordial pain at rest, which may precede a MYOCARDIAL INFARCTION. | 0 | 2.97 | 4 | 0 |
Cancer of the Tongue [description not available] | 0 | 4.15 | 6 | 0 |
Tongue Neoplasms Tumors or cancer of the TONGUE. | 0 | 4.15 | 6 | 0 |
Diseases, Metabolic [description not available] | 0 | 3.41 | 2 | 0 |
Metabolic Diseases Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed) | 0 | 3.41 | 2 | 0 |
Bladder Disorder, Neurogenic [description not available] | 0 | 2.52 | 2 | 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 | 2.52 | 2 | 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 | 2.46 | 2 | 0 |
Urinary Retention Inability to empty the URINARY BLADDER with voiding (URINATION). | 0 | 2.44 | 2 | 0 |
Inflammatory Breast Cancer [description not available] | 0 | 2.17 | 1 | 0 |
Inflammatory Breast Neoplasms Metastatic breast cancer characterized by EDEMA and ERYTHEMA of the affected breast due to LYMPHATIC METASTASIS and eventual obstruction of LYMPHATIC VESSELS by the cancer cells. | 0 | 2.17 | 1 | 0 |
Rupture Forcible or traumatic tear or break of an organ or other soft part of the body. | 0 | 10.41 | 14 | 0 |
Inferior Dislocation [description not available] | 0 | 2.94 | 4 | 0 |
Airway Remodeling The structural changes in the number, mass, size and/or composition of the airway tissues. | 0 | 2.17 | 1 | 0 |
Asthma, Bronchial [description not available] | 0 | 2.74 | 3 | 0 |
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 | 2.74 | 3 | 0 |
Adenohypophyseal Diseases [description not available] | 0 | 4.9 | 8 | 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 | 9.9 | 8 | 1 |
Injuries, Knee [description not available] | 0 | 6.03 | 10 | 1 |
Knee Injuries Injuries to the knee or the knee joint. | 0 | 6.03 | 10 | 1 |
Connective and Soft Tissue Neoplasms [description not available] | 0 | 2.53 | 2 | 0 |
Myxoid Liposarcoma [description not available] | 0 | 2.55 | 2 | 0 |
Liposarcoma, Myxoid A liposarcoma containing round mesenchymal cells and a myxoid extracellular matrix in stroma. | 0 | 2.55 | 2 | 0 |
Coxa Plana [description not available] | 0 | 4.35 | 7 | 0 |
Aseptic Necrosis of Femur Head [description not available] | 0 | 3.95 | 13 | 0 |
Tolosa-Hunt Syndrome An idiopathic syndrome characterized by the formation of granulation tissue in the anterior cavernous sinus or superior orbital fissure, producing a painful ophthalmoplegia. (Adams et al., Principles of Neurology, 6th ed, p271) | 0 | 3.14 | 5 | 0 |
Eye Pain A dull or sharp painful sensation associated with the outer or inner structures of the eyeball, having different causes. | 0 | 2.17 | 1 | 0 |
Pyrexia [description not available] | 0 | 6.89 | 15 | 1 |
Fever An abnormal elevation of body temperature, usually as a result of a pathologic process. | 0 | 6.89 | 15 | 1 |
Diverticula [description not available] | 0 | 2.73 | 3 | 0 |
Cardiac Murmurs [description not available] | 0 | 2.46 | 2 | 0 |
Biliary or Urinary Stones [description not available] | 0 | 3.09 | 1 | 0 |
Cholera Infantum [description not available] | 0 | 5.54 | 7 | 0 |
Testicular Diseases Pathological processes of the TESTIS. | 0 | 3.66 | 3 | 0 |
Blood Pressure, Low [description not available] | 0 | 3.1 | 5 | 0 |
Hypotension Abnormally low BLOOD PRESSURE that can result in inadequate blood flow to the brain and other vital organs. Common symptom is DIZZINESS but greater negative impacts on the body occur when there is prolonged depravation of oxygen and nutrients. | 0 | 3.1 | 5 | 0 |
Anomalous Ventricular Excitation Syndrome [description not available] | 0 | 2.17 | 1 | 0 |
Wolff-Parkinson-White Syndrome A form of ventricular pre-excitation characterized by a short PR interval and a long QRS interval with a delta wave. In this syndrome, atrial impulses are abnormally conducted to the HEART VENTRICLES via an ACCESSORY CONDUCTING PATHWAY that is located between the wall of the right or left atria and the ventricles, also known as a BUNDLE OF KENT. The inherited form can be caused by mutation of PRKAG2 gene encoding a gamma-2 regulatory subunit of AMP-activated protein kinase. | 0 | 2.17 | 1 | 0 |
Peripheral Arterial Diseases [description not available] | 0 | 7.37 | 13 | 1 |
Peripheral Arterial Disease Lack of perfusion in the EXTREMITIES resulting from atherosclerosis. It is characterized by INTERMITTENT CLAUDICATION, and an ANKLE BRACHIAL INDEX of 0.9 or less. | 0 | 7.37 | 13 | 1 |
Blood Loss, Surgical Loss of blood during a surgical procedure. | 0 | 2.17 | 1 | 0 |
Craniofacial Pain Syndromes [description not available] | 0 | 3.36 | 2 | 0 |
Arterial Obstructive Diseases [description not available] | 0 | 11.63 | 62 | 6 |
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 | 11.63 | 62 | 6 |
Cervical Spondylosis [description not available] | 0 | 3.38 | 6 | 0 |
Spondylosis A degenerative spinal disease that can involve any part of the VERTEBRA, the INTERVERTEBRAL DISK, and the surrounding soft tissue. | 0 | 8.38 | 6 | 0 |
Sterility, Female [description not available] | 0 | 3.88 | 2 | 1 |
Endometrial Diseases [description not available] | 0 | 4.11 | 3 | 1 |
Fallopian Tube Diseases Diseases involving the FALLOPIAN TUBES including neoplasms (FALLOPIAN TUBE NEOPLASMS); SALPINGITIS; tubo-ovarian abscess; and blockage. | 0 | 3.82 | 2 | 1 |
Abnormalities, Urogenital [description not available] | 0 | 3.59 | 1 | 1 |
Infertility, Female Diminished or absent ability of a female to achieve conception. | 0 | 3.88 | 2 | 1 |
Uterine Diseases Pathological processes involving any part of the UTERUS. | 0 | 4.11 | 3 | 1 |
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 | 4.12 | 3 | 0 |
Hemisensory Neglect [description not available] | 0 | 2.44 | 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 | 2.44 | 2 | 0 |
Epileptiform Neuralgia [description not available] | 0 | 6.27 | 13 | 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 | 6.27 | 13 | 0 |
Complications, Neoplastic Pregnancy [description not available] | 0 | 3.72 | 3 | 0 |
Otospongiosis [description not available] | 0 | 3.29 | 6 | 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 | 3.29 | 6 | 0 |
Fibroadenoma An adenoma containing fibrous tissue. It should be differentiated from ADENOFIBROMA which is a tumor composed of connective tissue (fibroma) containing glandular (adeno-) structures. (From Dorland, 27th ed) | 0 | 4.71 | 11 | 0 |
Carcinoma, Ductal, Breast An invasive (infiltrating) CARCINOMA of the mammary ductal system (MAMMARY GLANDS) in the human BREAST. | 0 | 6.26 | 19 | 0 |
Reproductive Sterility [description not available] | 0 | 2.17 | 1 | 0 |
Infertility A reduced or absent capacity to reproduce. | 0 | 7.17 | 1 | 0 |
Abscess, Epidural [description not available] | 0 | 5.81 | 9 | 0 |
Congenital Zika Syndrome [description not available] | 0 | 2.17 | 1 | 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 | 2.17 | 1 | 0 |
Intermittent Claudication A symptom complex characterized by pain and weakness in SKELETAL MUSCLE group associated with exercise, such as leg pain and weakness brought on by walking. Such muscle limpness disappears after a brief rest and is often relates to arterial STENOSIS; muscle ISCHEMIA; and accumulation of LACTATE. | 0 | 4.67 | 6 | 1 |
Experimental Mammary Neoplasms [description not available] | 0 | 4.83 | 32 | 0 |
Cancer of Gastrointestinal Tract [description not available] | 0 | 4.09 | 3 | 0 |
Atrophic Muscular Disorders [description not available] | 0 | 2.21 | 1 | 0 |
Cardiovascular Pregnancy Complications [description not available] | 0 | 3.88 | 2 | 0 |
Coronary Heart Disease [description not available] | 0 | 15.1 | 116 | 2 |
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 | 15.1 | 116 | 2 |
Mitral Stenosis [description not available] | 0 | 7.73 | 3 | 0 |
Bouillaud Disease [description not available] | 0 | 2.83 | 3 | 0 |
Mitral Valve Stenosis Narrowing of the passage through the MITRAL VALVE due to FIBROSIS, and CALCINOSIS in the leaflets and chordal areas. This elevates the left atrial pressure which, in turn, raises pulmonary venous and capillary pressure leading to bouts of DYSPNEA and TACHYCARDIA during physical exertion. RHEUMATIC FEVER is its primary cause. | 0 | 2.73 | 3 | 0 |
Rheumatic Heart Disease Cardiac manifestation of systemic rheumatological conditions, such as RHEUMATIC FEVER. Rheumatic heart disease can involve any part the heart, most often the HEART VALVES and the ENDOCARDIUM. | 0 | 2.83 | 3 | 0 |
Bilateral Wilms Tumor [description not available] | 0 | 2.21 | 1 | 0 |
Wilms Tumor A malignant kidney tumor, caused by the uncontrolled multiplication of renal stem (blastemal), stromal (STROMAL CELLS), and epithelial (EPITHELIAL CELLS) elements. However, not all three are present in every case. Several genes or chromosomal areas have been associated with Wilms tumor which is usually found in childhood as a firm lump in a child's side or ABDOMEN. | 0 | 2.21 | 1 | 0 |
Esophageal Diseases Pathological processes in the ESOPHAGUS. | 0 | 3.09 | 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 | 2.5 | 2 | 0 |
Urinary Lithiasis [description not available] | 0 | 4 | 2 | 0 |
Perforated Appendicitis [description not available] | 0 | 5.31 | 4 | 0 |
Colicky Pain [description not available] | 0 | 5.43 | 5 | 1 |
Placenta Diseases Pathological processes or abnormal functions of the PLACENTA. | 0 | 3.48 | 2 | 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 | 3.12 | 1 | 0 |
Placental Abruption [description not available] | 0 | 3.12 | 1 | 0 |
Abruptio Placentae Premature separation of the normally implanted PLACENTA from the UTERUS. Signs of varying degree of severity include UTERINE BLEEDING, uterine MUSCLE HYPERTONIA, and FETAL DISTRESS or FETAL DEATH. | 0 | 3.12 | 1 | 0 |
Appendicitis Acute inflammation of the APPENDIX. Acute appendicitis is classified as simple, gangrenous, or perforated. | 0 | 5.31 | 4 | 0 |
Abdominal Pain Sensation of discomfort, distress, or agony in the abdominal region. | 0 | 5.43 | 5 | 1 |
Urolithiasis Formation of stones in any part of the URINARY TRACT, usually in the KIDNEY; URINARY BLADDER; or the URETER. | 0 | 4 | 2 | 0 |
Asymmetric Septal Hypertrophy, Familial [description not available] | 0 | 3.32 | 6 | 0 |
Multiple Primary Neoplasms [description not available] | 0 | 6.03 | 10 | 1 |
Child Development Deviations [description not available] | 0 | 3.12 | 1 | 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 | 3.12 | 1 | 0 |
Congenital Dysplasia Of The Hip [description not available] | 0 | 3.11 | 5 | 0 |
Degenerative Disc Disease [description not available] | 0 | 4.44 | 4 | 1 |
Neuralgia, Sciatic [description not available] | 0 | 6.27 | 7 | 2 |
Sciatica A condition characterized by pain radiating from the back into the buttock and posterior/lateral aspects of the leg. Sciatica may be a manifestation of SCIATIC NEUROPATHY; RADICULOPATHY (involving the SPINAL NERVE ROOTS; L4, L5, S1, or S2, often associated with INTERVERTEBRAL DISK DISPLACEMENT); or lesions of the CAUDA EQUINA. | 0 | 6.27 | 7 | 2 |
Intervertebral Disc Degeneration Degenerative changes in the INTERVERTEBRAL DISC due to aging or structural damage, especially to the vertebral end-plates. | 0 | 4.44 | 4 | 1 |
Dermatitis Medicamentosa [description not available] | 0 | 4.36 | 7 | 0 |
Cockett Syndrome [description not available] | 0 | 2.21 | 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 | 2.43 | 2 | 0 |
Osteogenic Sarcoma [description not available] | 0 | 5.12 | 17 | 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 | 5.12 | 17 | 0 |
Brain Vascular Disorders [description not available] | 0 | 9.37 | 36 | 1 |
Cerebrovascular Disorders A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others. | 0 | 9.37 | 36 | 1 |
Infarct, Lacunar [description not available] | 0 | 2.61 | 2 | 0 |
Adnexitis Inflammation of the uterine appendages (ADNEXA UTERI) including infection of the FALLOPIAN TUBES (SALPINGITIS), the ovaries (OOPHORITIS), or the supporting ligaments (PARAMETRITIS). | 0 | 3.12 | 1 | 0 |
Empyema, Gall Bladder [description not available] | 0 | 3.12 | 1 | 0 |
Primary Peritonitis [description not available] | 0 | 4.96 | 5 | 0 |
Necrotizing Pyelonephritis [description not available] | 0 | 3.86 | 4 | 0 |
Pelvic Inflammatory Disease A spectrum of inflammation involving the female upper genital tract and the supporting tissues. It is usually caused by an ascending infection of organisms from the endocervix. Infection may be confined to the uterus (ENDOMETRITIS), the FALLOPIAN TUBES; (SALPINGITIS); the ovaries (OOPHORITIS), the supporting ligaments (PARAMETRITIS), or may involve several of the above uterine appendages. Such inflammation can lead to functional impairment and infertility. | 0 | 3.12 | 1 | 0 |
Cholecystitis Inflammation of the GALLBLADDER; generally caused by impairment of BILE flow, GALLSTONES in the BILIARY TRACT, infections, or other diseases. | 0 | 3.12 | 1 | 0 |
Peritonitis INFLAMMATION of the PERITONEUM lining the ABDOMINAL CAVITY as the result of infectious, autoimmune, or chemical processes. Primary peritonitis is due to infection of the PERITONEAL CAVITY via hematogenous or lymphatic spread and without intra-abdominal source. Secondary peritonitis arises from the ABDOMINAL CAVITY itself through RUPTURE or ABSCESS of intra-abdominal organs. | 0 | 9.96 | 5 | 0 |
Pyelonephritis Inflammation of the KIDNEY involving the renal parenchyma (the NEPHRONS); KIDNEY PELVIS; and KIDNEY CALICES. It is characterized by ABDOMINAL PAIN; FEVER; NAUSEA; VOMITING; and occasionally DIARRHEA. | 0 | 8.86 | 4 | 0 |
Cranial Airocele [description not available] | 0 | 2.49 | 2 | 0 |
Mastoiditis Inflammation of the honeycomb-like MASTOID BONE in the skull just behind the ear. It is usually a complication of OTITIS MEDIA. | 0 | 2.93 | 4 | 0 |
Angioneurotic Edema [description not available] | 0 | 2.21 | 1 | 0 |
Hives [description not available] | 0 | 2.99 | 4 | 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 | 2.21 | 1 | 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 | 2.99 | 4 | 0 |
Urinary Tract Diseases [description not available] | 0 | 7.17 | 9 | 1 |
Adrenal Gland Hypofunction [description not available] | 0 | 2.21 | 1 | 0 |
Adrenal Insufficiency Conditions in which the production of adrenal CORTICOSTEROIDS falls below the requirement of the body. Adrenal insufficiency can be caused by defects in the ADRENAL GLANDS, the PITUITARY GLAND, or the HYPOTHALAMUS. | 0 | 2.21 | 1 | 0 |
Aspiration, Respiratory [description not available] | 0 | 2.21 | 1 | 0 |
Fetal Death Death of the developing young in utero. BIRTH of a dead FETUS is STILLBIRTH. | 0 | 2.46 | 2 | 0 |
Cytomegalic Inclusion Disease [description not available] | 0 | 3.25 | 6 | 0 |
Central Nervous System Viral Diseases Viral infections of the brain, spinal cord, meninges, or perimeningeal spaces. | 0 | 2.21 | 1 | 0 |
Cytomegalovirus Infections Infection with CYTOMEGALOVIRUS, characterized by enlarged cells bearing intranuclear inclusions. Infection may be in almost any organ, but the salivary glands are the most common site in children, as are the lungs in adults. | 0 | 3.25 | 6 | 0 |
Acquired Encephalocele [description not available] | 0 | 2.78 | 3 | 0 |
B-Cell Lymphoma [description not available] | 0 | 4.44 | 8 | 0 |
Peripheral Nerve Neoplasms [description not available] | 0 | 4.03 | 14 | 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 | 4.03 | 14 | 0 |
Lymphoma, B-Cell A group of heterogeneous lymphoid tumors generally expressing one or more B-cell antigens or representing malignant transformations of B-lymphocytes. | 0 | 4.44 | 8 | 0 |
Atrophy, Muscular, Peroneal [description not available] | 0 | 2.44 | 2 | 0 |
Charcot-Marie-Tooth Disease A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343) | 0 | 2.44 | 2 | 0 |
Prostatic Diseases Pathological processes involving the PROSTATE or its component tissues. | 0 | 5 | 3 | 1 |
Congenital Varicella Syndrome [description not available] | 0 | 2.21 | 1 | 0 |
Anal Cancer [description not available] | 0 | 2.21 | 1 | 0 |
Rectovaginal Fistula An abnormal anatomical passage between the RECTUM and the VAGINA. | 0 | 2.21 | 1 | 0 |
Anus Neoplasms Tumors or cancer of the ANAL CANAL. | 0 | 2.21 | 1 | 0 |
Amnesia, Transient Global A syndrome characterized by a transient loss of the ability to form new memories. It primarily occurs in middle aged or elderly individuals, and episodes may last from minutes to hours. During the period of amnesia, immediate and recent memory abilities are impaired, but the level of consciousness and ability to perform other intellectual tasks are preserved. The condition is related to bilateral dysfunction of the medial portions of each TEMPORAL LOBE. Complete recovery normally occurs, and recurrences are unusual. (From Adams et al., Principles of Neurology, 6th ed, pp429-30) | 0 | 2.21 | 1 | 0 |
Diffuse Myofascial Pain Syndrome [description not available] | 0 | 2.49 | 2 | 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 | 7.49 | 2 | 0 |
Animal Mammary Carcinoma [description not available] | 0 | 3.15 | 5 | 0 |
Ileitis Inflammation of any segment of the ILEUM and the ILEOCECAL VALVE. | 0 | 4.13 | 3 | 1 |
Vascular Calcification Deposition of calcium into the blood vessel structures. Excessive calcification of the vessels are associated with ATHEROSCLEROTIC PLAQUES formation particularly after MYOCARDIAL INFARCTION (see MONCKEBERG MEDIAL CALCIFIC SCLEROSIS) and chronic kidney diseases which in turn increase VASCULAR STIFFNESS. | 0 | 2.51 | 2 | 0 |
Calcification, Pathologic [description not available] | 0 | 8.05 | 29 | 0 |
Calcinosis Pathologic deposition of calcium salts in tissues. | 0 | 8.05 | 29 | 0 |
Sclerosis A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve. | 0 | 5.71 | 7 | 1 |
Acute Inferior Myocardial Infarction [description not available] | 0 | 2.11 | 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 | 2.43 | 2 | 0 |
Compression Fractures [description not available] | 0 | 7.96 | 4 | 0 |
Spondylitis Inflammation of the SPINE. This includes both arthritic and non-arthritic conditions. | 0 | 4.31 | 7 | 0 |
ANS (Autonomic Nervous System) Diseases [description not available] | 0 | 2.08 | 1 | 0 |
Chronic Lymphocytic Thyroiditis [description not available] | 0 | 2.48 | 2 | 0 |
Hashimoto Disease Chronic autoimmune thyroiditis, characterized by the presence of high serum thyroid AUTOANTIBODIES; GOITER; and HYPOTHYROIDISM. | 0 | 2.48 | 2 | 0 |
Cancer of Intestines [description not available] | 0 | 3.67 | 3 | 0 |
Intestinal Neoplasms Tumors or cancer of the INTESTINES. | 0 | 3.67 | 3 | 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 | 4.54 | 9 | 0 |
Insulin Sensitivity [description not available] | 0 | 3.32 | 6 | 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 | 3.32 | 6 | 0 |
Alogia [description not available] | 0 | 2.45 | 2 | 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 | 2.45 | 2 | 0 |
Day Blindness [description not available] | 0 | 6.52 | 12 | 0 |
Toxocariasis Infection by round worms of the genus TOXOCARA, usually found in wild and domesticated cats and dogs and foxes, except for the larvae, which may produce visceral and ocular larva migrans in man. | 0 | 2.08 | 1 | 0 |
Cochlear Diseases Pathological processes of the snail-like structure (COCHLEA) of the inner ear (LABYRINTH) which can involve its nervous tissue, blood vessels, or fluid (ENDOLYMPH). | 0 | 2.94 | 4 | 0 |
Cystic Fibrosis of Pancreas [description not available] | 0 | 3.85 | 4 | 0 |
Cystic Fibrosis An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION. | 0 | 3.85 | 4 | 0 |
Biliary Tract Diseases Diseases in any part of the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 9.99 | 6 | 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 | 2.08 | 1 | 0 |
Anaplastic Oligodendroglioma [description not available] | 0 | 6.33 | 14 | 1 |
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 | 6.33 | 14 | 1 |
Neoplasms, Bone Marrow [description not available] | 0 | 3.85 | 4 | 0 |
Bone Marrow Neoplasms Neoplasms located in the bone marrow. They are differentiated from neoplasms composed of bone marrow cells, such as MULTIPLE MYELOMA. Most bone marrow neoplasms are metastatic. | 0 | 3.85 | 4 | 0 |
Amniotic Fluid Embolism [description not available] | 0 | 2.08 | 1 | 0 |
Adipose Tissue Neoplasms [description not available] | 0 | 2.08 | 1 | 0 |
Thoracic Diseases Disorders affecting the organs of the thorax. | 0 | 3.39 | 2 | 0 |
Diseases, Peripheral Vascular [description not available] | 0 | 13.22 | 49 | 6 |
Peripheral Vascular Diseases Pathological processes involving any one of the BLOOD VESSELS in the vasculature outside the HEART. | 0 | 13.22 | 49 | 6 |
Epidermal Cyst Intradermal or subcutaneous saclike structure, the wall of which is stratified epithelium containing keratohyalin granules. | 0 | 4.71 | 11 | 0 |
Brain Emboli [description not available] | 0 | 2.72 | 3 | 0 |
Infarct of the Spleen [description not available] | 0 | 2.08 | 1 | 0 |
Situs Inversus A congenital abnormality in which organs in the THORAX and the ABDOMEN are opposite to their normal positions (situs solitus) due to lateral transposition. Normally the STOMACH and SPLEEN are on the left, LIVER on the right, the three-lobed right lung is on the right, and the two-lobed left lung on the left. Situs inversus has a familial pattern and has been associated with a number of genes related to microtubule-associated proteins. | 0 | 2.08 | 1 | 0 |
Asplenia Syndrome [description not available] | 0 | 2.51 | 2 | 0 |
Splenic Diseases Diseases involving the SPLEEN. | 0 | 4.99 | 9 | 1 |
Solitary Fibrous Tumors Rare neoplasms of mesenchymal origin, usually benign, and most commonly involving the PLEURA (see SOLITARY FIBROUS TUMOR, PLEURAL). They also are found in extrapleural sites. | 0 | 2.08 | 1 | 0 |
Nasopharyngeal Carcinoma A carcinoma that originates in the EPITHELIUM of the NASOPHARYNX and includes four subtypes: keratinizing squamous cell, non-keratinizing, basaloid squamous cell, and PAPILLARY ADENOCARCINOMA. It is most prevalent in Southeast Asian populations and is associated with EPSTEIN-BARR VIRUS INFECTIONS. Somatic mutations associated with this cancer have been identified in NPCR, BAP1, UBAP1, ERBB2, ERBB3, MLL2, PIK3CA, KRAS, NRAS, and ARID1A genes. | 0 | 2.51 | 2 | 0 |
Adhesive Capsulitis [description not available] | 0 | 5.42 | 5 | 1 |
Injuries, Tendon [description not available] | 0 | 5 | 9 | 0 |
Coracohumeral Impingement [description not available] | 0 | 3.34 | 2 | 0 |
Bursitis Inflammation or irritation of a SYNOVIAL BURSA, the fibrous sac that acts as a cushion between moving structures of bones, muscles, tendons or skin. | 0 | 5.42 | 5 | 1 |
Shoulder Impingement Syndrome Compression of the ROTATOR CUFF tendons and subacromial bursa between the HUMERAL HEAD and the ACROMION of the SCAPULA. This condition is associated with subacromial BURSITIS, as well as rotator cuff (largely supraspinatus) and bicipital tendon INFLAMMATION. | 0 | 3.34 | 2 | 0 |
Shoulder Pain Unilateral or bilateral pain of the shoulder. It is often caused by physical activities such as work or sports participation, but may also be pathologic in origin. | 0 | 5.03 | 3 | 1 |
Ewing Sarcoma [description not available] | 0 | 4.53 | 3 | 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 | 4.53 | 3 | 0 |
Beriberi, Cerebral [description not available] | 0 | 3.11 | 5 | 0 |
Carotid Artery Dissection, Internal [description not available] | 0 | 5.25 | 4 | 1 |
AIDS-Associated Lymphoma [description not available] | 0 | 3.25 | 6 | 0 |
Lymphoma, AIDS-Related B-cell lymphoid tumors that occur in association with AIDS. Patients often present with an advanced stage of disease and highly malignant subtypes including BURKITT LYMPHOMA; IMMUNOBLASTIC LARGE-CELL LYMPHOMA; PRIMARY EFFUSION LYMPHOMA; and DIFFUSE, LARGE B-CELL, LYMPHOMA. The tumors are often disseminated in unusual extranodal sites and chromosomal abnormalities are frequently present. It is likely that polyclonal B-cell lymphoproliferation in AIDS is a complex result of EBV infection, HIV antigenic stimulation, and T-cell-dependent HIV activation. | 0 | 3.25 | 6 | 0 |
Hematochezia The passage of bright red blood from the rectum. The blood may or may not be mixed with formed stool in the form of blood, blood clots, bloody stool or diarrhea. | 0 | 2.77 | 3 | 0 |
Anorectal Diseases [description not available] | 0 | 2.7 | 3 | 0 |
Gastrointestinal Hemorrhage Bleeding in any segment of the GASTROINTESTINAL TRACT from ESOPHAGUS to RECTUM. | 0 | 2.77 | 3 | 0 |
Rectal Diseases Pathological developments in the RECTUM region of the large intestine (INTESTINE, LARGE). | 0 | 2.7 | 3 | 0 |
Convulsions, Grand Mal [description not available] | 0 | 2.48 | 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 | 2.48 | 2 | 0 |
Sore Throat [description not available] | 0 | 2.08 | 1 | 0 |
Aprosodia [description not available] | 0 | 2.44 | 2 | 0 |
Pharyngitis Inflammation of the throat (PHARYNX). | 0 | 2.08 | 1 | 0 |
Agnosia Loss of the ability to comprehend the meaning or recognize the importance of various forms of stimulation that cannot be attributed to impairment of a primary sensory modality. Tactile agnosia is characterized by an inability to perceive the shape and nature of an object by touch alone, despite unimpaired sensation to light touch, position, and other primary sensory modalities. | 0 | 2.1 | 1 | 0 |
Hypertrophy, Right Ventricular Enlargement of the RIGHT VENTRICLE of the heart. This increase in ventricular mass is often attributed to PULMONARY HYPERTENSION and is a contributor to cardiovascular morbidity and mortality. | 0 | 3.64 | 3 | 0 |
Paralysis, Legs [description not available] | 0 | 3.5 | 8 | 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 | 3.5 | 8 | 0 |
Carcinoma, Thymic [description not available] | 0 | 3.34 | 2 | 0 |
Cancer of the Thymus [description not available] | 0 | 3.34 | 2 | 0 |
Thymoma A neoplasm originating from thymic tissue, usually benign, and frequently encapsulated. Although it is occasionally invasive, metastases are extremely rare. It consists of any type of thymic epithelial cell as well as lymphocytes that are usually abundant. Malignant lymphomas that involve the thymus, e.g., lymphosarcoma, Hodgkin's disease (previously termed granulomatous thymoma), should not be regarded as thymoma. (From Stedman, 25th ed) | 0 | 3.34 | 2 | 0 |
Thymus Neoplasms Tumors or cancer of the THYMUS GLAND. | 0 | 3.34 | 2 | 0 |
Aneurysm, Iliac [description not available] | 0 | 2.7 | 3 | 0 |
Cranial Nerve IV Diseases [description not available] | 0 | 3.39 | 2 | 0 |
Brown Tendon Sheath Syndrome [description not available] | 0 | 4.18 | 6 | 0 |
Affective Psychosis, Bipolar [description not available] | 0 | 2.41 | 2 | 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 | 2.41 | 2 | 0 |
Angioma, Venous, Central Nervous System [description not available] | 0 | 2.08 | 1 | 0 |
Heavy Menstrual Bleeding [description not available] | 0 | 2.1 | 1 | 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 | 10.68 | 19 | 0 |
Menorrhagia Excessive uterine bleeding during MENSTRUATION. | 0 | 2.1 | 1 | 0 |
Hibernation, Myocardial [description not available] | 0 | 6.27 | 9 | 0 |
Connective Tissue Diseases A heterogeneous group of disorders, some hereditary, others acquired, characterized by abnormal structure or function of one or more of the elements of connective tissue, i.e., collagen, elastin, or the mucopolysaccharides. | 0 | 3.12 | 5 | 0 |
Erythrophagocytic Lymphohistiocytosis, Familial [description not available] | 0 | 2.1 | 1 | 0 |
Lymphohistiocytosis, Hemophagocytic A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive. | 0 | 2.1 | 1 | 0 |
Benign Cerebellar Neoplasms [description not available] | 0 | 8.98 | 41 | 1 |
Arachnoidal Cerebellar Sarcoma, Circumscribed [description not available] | 0 | 5.25 | 12 | 1 |
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 | 3.4 | 7 | 0 |
Medulloblastoma A malignant neoplasm that may be classified either as a glioma or as a primitive neuroectodermal tumor of childhood (see NEUROECTODERMAL TUMOR, PRIMITIVE). The tumor occurs most frequently in the first decade of life with the most typical location being the cerebellar vermis. Histologic features include a high degree of cellularity, frequent mitotic figures, and a tendency for the cells to organize into sheets or form rosettes. Medulloblastoma have a high propensity to spread throughout the craniospinal intradural axis. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2060-1) | 0 | 5.25 | 12 | 1 |
Entrapment Neuropathies [description not available] | 0 | 4.64 | 10 | 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 | 2.08 | 1 | 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 | 3.51 | 8 | 0 |
Ulna Fractures Fractures of the larger bone of the forearm. | 0 | 3.01 | 1 | 0 |
Femoral Fractures Fractures of the femur. | 0 | 5.86 | 8 | 0 |
Segond Fracture [description not available] | 0 | 5.49 | 6 | 0 |
Humeral Fractures Fractures of the HUMERUS. | 0 | 3.01 | 1 | 0 |
Tibial Fractures Fractures of the TIBIA. | 0 | 5.49 | 6 | 0 |
Angiomatosis Oculoorbital-Thalamic Syndrome [description not available] | 0 | 3.4 | 7 | 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 | 8.4 | 7 | 0 |
Linitis Plastica A condition where the stomach wall becomes thickened, rubbery and loses its ability to distend. The stomach assumes a leather bottle shape. It is most often seen in adenocarcinoma of the stomach. The term is often used synonymously with diffuse adenocarcinoma of the stomach. | 0 | 2.1 | 1 | 0 |
Central Pontine Myelinolysis [description not available] | 0 | 2.49 | 2 | 0 |
Bewilderment [description not available] | 0 | 2.95 | 4 | 0 |
Decreased Muscle Tone [description not available] | 0 | 2.49 | 2 | 0 |
Multiple Hemangioblastomas [description not available] | 0 | 5.1 | 10 | 1 |
Hemangioblastoma A benign tumor of the nervous system that may occur sporadically or in association with VON HIPPEL-LINDAU DISEASE. It accounts for approximately 2% of intracranial tumors, arising most frequently in the cerebellar hemispheres and vermis. Histologically, the tumors are composed of multiple capillary and sinusoidal channels lined with endothelial cells and clusters of lipid-laden pseudoxanthoma cells. Usually solitary, these tumors can be multiple and may also occur in the brain stem, spinal cord, retina, and supratentorial compartment. Cerebellar hemangioblastomas usually present in the third decade with INTRACRANIAL HYPERTENSION, and ataxia. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2071-2) | 0 | 5.1 | 10 | 1 |
Acute Brain Injuries [description not available] | 0 | 9.38 | 10 | 5 |
Absence Status [description not available] | 0 | 3.28 | 6 | 0 |
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 | 9.38 | 10 | 5 |
Status Epilepticus A prolonged seizure or seizures repeated frequently enough to prevent recovery between episodes occurring over a period of 20-30 minutes. The most common subtype is generalized tonic-clonic status epilepticus, a potentially fatal condition associated with neuronal injury and respiratory and metabolic dysfunction. Nonconvulsive forms include petit mal status and complex partial status, which may manifest as behavioral disturbances. Simple partial status epilepticus consists of persistent motor, sensory, or autonomic seizures that do not impair cognition (see also EPILEPSIA PARTIALIS CONTINUA). Subclinical status epilepticus generally refers to seizures occurring in an unresponsive or comatose individual in the absence of overt signs of seizure activity. (From N Engl J Med 1998 Apr 2;338(14):970-6; Neurologia 1997 Dec;12 Suppl 6:25-30) | 0 | 3.28 | 6 | 0 |
Brain Ventricular Neoplasms [description not available] | 0 | 5 | 9 | 0 |
Nephritis Inflammation of any part of the KIDNEY. | 0 | 9.08 | 3 | 1 |
Encephalitis, Viral Inflammation of brain parenchymal tissue as a result of viral infection. Encephalitis may occur as primary or secondary manifestation of TOGAVIRIDAE INFECTIONS; HERPESVIRIDAE INFECTIONS; ADENOVIRIDAE INFECTIONS; FLAVIVIRIDAE INFECTIONS; BUNYAVIRIDAE INFECTIONS; PICORNAVIRIDAE INFECTIONS; PARAMYXOVIRIDAE INFECTIONS; ORTHOMYXOVIRIDAE INFECTIONS; RETROVIRIDAE INFECTIONS; and ARENAVIRIDAE INFECTIONS. | 0 | 4.53 | 9 | 0 |
Dejerine-Roussy Syndrome [description not available] | 0 | 2.42 | 2 | 0 |
Carcinogenesis The origin, production or development of cancer through genotypic and phenotypic changes which upset the normal balance between cell proliferation and cell death. Carcinogenesis generally requires a constellation of steps, which may occur quickly or over a period of many years. | 0 | 2.08 | 1 | 0 |
Cancer of Cervix [description not available] | 0 | 9.37 | 25 | 2 |
Uterine Cervical Neoplasms Tumors or cancer of the UTERINE CERVIX. | 0 | 9.37 | 25 | 2 |
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 | 2.1 | 1 | 0 |
Glioblastoma with Sarcomatous Component [description not available] | 0 | 3.15 | 5 | 0 |
Gliosarcoma Rare mixed tumors of the brain and rarely the spinal cord which contain malignant neuroectodermal (glial) and mesenchymal components, including spindle-shaped fibrosarcoma cells. These tumors are highly aggressive and present primarily in adults as rapidly expanding mass lesions. They may arise in tissue that has been previously irradiated. (From Br J Neurosurg 1995 Apr;9(2):171-8) | 0 | 3.15 | 5 | 0 |
Goldblatt Syndrome [description not available] | 0 | 6.65 | 17 | 0 |
Hypertension, Renovascular Hypertension due to RENAL ARTERY OBSTRUCTION or compression. | 0 | 6.65 | 17 | 0 |
Anterior Circulation Transient Ischemic Attack [description not available] | 0 | 3.7 | 10 | 0 |
Ischemic Attack, Transient Brief reversible episodes of focal, nonconvulsive ischemic dysfunction of the brain having a duration of less than 24 hours, and usually less than one hour, caused by transient thrombotic or embolic blood vessel occlusion or stenosis. Events may be classified by arterial distribution, temporal pattern, or etiology (e.g., embolic vs. thrombotic). (From Adams et al., Principles of Neurology, 6th ed, pp814-6) | 0 | 3.7 | 10 | 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 | 8.39 | 7 | 0 |
Synovial Cyst Non-neoplastic tumor-like lesions at joints, developed from the SYNOVIAL MEMBRANE of a joint through the JOINT CAPSULE into the periarticular tissues. They are filled with SYNOVIAL FLUID with a smooth and translucent appearance. A synovial cyst can develop from any joint, but most commonly at the back of the knee, where it is known as POPLITEAL CYST. | 0 | 8.51 | 8 | 0 |
Hydrosyringomyelia [description not available] | 0 | 4.18 | 6 | 0 |
Arnold-Chiari Deformity [description not available] | 0 | 2.1 | 1 | 0 |
Injuries, Whiplash [description not available] | 0 | 2.1 | 1 | 0 |
Pulsatile Tinnitus [description not available] | 0 | 4.33 | 7 | 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 | 4.33 | 7 | 0 |
Polychondritis, Chronic Atrophic [description not available] | 0 | 2.1 | 1 | 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 | 2.1 | 1 | 0 |
Aberrant Tissue [description not available] | 0 | 4.02 | 5 | 0 |
Orbital Diseases Diseases of the bony orbit and contents except the eyeball. | 0 | 5.46 | 15 | 0 |
Epithelial Neoplasms [description not available] | 0 | 3.63 | 3 | 0 |
Teeth, Devitalized [description not available] | 0 | 2.1 | 1 | 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 | 2.1 | 1 | 0 |
Bone Spur [description not available] | 0 | 2.1 | 1 | 0 |
Adenomyosis The extension of endometrial tissue (ENDOMETRIUM) into the MYOMETRIUM. It usually occurs in women in their reproductive years and may result in a diffusely enlarged uterus with ectopic and benign endometrial glands and stroma. | 0 | 3.89 | 2 | 1 |
Carcinoma, Colloid [description not available] | 0 | 2.11 | 1 | 0 |
Adenocarcinoma, Mucinous An adenocarcinoma producing mucin in significant amounts. (From Dorland, 27th ed) | 0 | 2.11 | 1 | 0 |
CBS Deficiency [description not available] | 0 | 2.11 | 1 | 0 |
Developmental Psychomotor Disorders [description not available] | 0 | 2.11 | 1 | 0 |
Homocystinuria Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979) | 0 | 2.11 | 1 | 0 |
Agnogenic Myeloid Metaplasia [description not available] | 0 | 2.1 | 1 | 0 |
Primary Myelofibrosis A de novo myeloproliferation arising from an abnormal stem cell. It is characterized by the replacement of bone marrow by fibrous tissue, a process that is mediated by CYTOKINES arising from the abnormal clone. | 0 | 2.1 | 1 | 0 |
Hand-Schu00FCller-Christian Disease [description not available] | 0 | 4.43 | 8 | 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 | 4.43 | 8 | 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 | 10.01 | 15 | 0 |
Cancer, Radiation-Induced [description not available] | 0 | 2.95 | 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 | 9.75 | 52 | 5 |
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 | 9.75 | 52 | 5 |
Hypothermia, Accidental [description not available] | 0 | 2.49 | 2 | 0 |
Acute Hemolytic Transfusion Reaction [description not available] | 0 | 2.1 | 1 | 0 |
Hypothermia Lower than normal body temperature, especially in warm-blooded animals. | 0 | 2.49 | 2 | 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 | 2.1 | 1 | 0 |
Adult Spinal Muscular Atrophy [description not available] | 0 | 2.1 | 1 | 0 |
Spinal Curvatures Deformities of the SPINE characterized by abnormal bending or flexure in the vertebral column. They may be bending forward (KYPHOSIS), backward (LORDOSIS), or sideway (SCOLIOSIS). | 0 | 2.1 | 1 | 0 |
Muscular Atrophy, Spinal A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089) | 0 | 2.1 | 1 | 0 |
Cancer of Nose [description not available] | 0 | 4.5 | 5 | 0 |
Acute Promyelocytic Leukemia [description not available] | 0 | 2.1 | 1 | 0 |
Leukemia, Promyelocytic, Acute An acute myeloid leukemia in which abnormal PROMYELOCYTES predominate. It is frequently associated with DISSEMINATED INTRAVASCULAR COAGULATION. | 0 | 2.1 | 1 | 0 |
Acidosis, Diabetic [description not available] | 0 | 2.1 | 1 | 0 |
Mucorales Infection [description not available] | 0 | 2.1 | 1 | 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 | 2.1 | 1 | 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 | 2.1 | 1 | 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 | 2.1 | 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 | 2.48 | 2 | 0 |
Anti-MuSK Myasthenia Gravis [description not available] | 0 | 2.42 | 2 | 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 | 7.42 | 2 | 0 |
Osteochondritis Dissecans A type of osteochondritis in which articular cartilage and associated bone becomes partially or totally detached to form joint loose bodies. Affects mainly the knee, ankle, and elbow joints. | 0 | 4.08 | 3 | 1 |
Bucket Handle Tears [description not available] | 0 | 3.11 | 5 | 0 |
Anemia, Fanconi [description not available] | 0 | 2.1 | 1 | 0 |
Leiomyosarcoma, Epithelioid [description not available] | 0 | 3.86 | 4 | 0 |
Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004) | 0 | 2.1 | 1 | 0 |
Leiomyosarcoma A sarcoma containing large spindle cells of smooth muscle. Although it rarely occurs in soft tissue, it is common in the viscera. It is the most common soft tissue sarcoma of the gastrointestinal tract and uterus. The median age of patients is 60 years. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1865) | 0 | 3.86 | 4 | 0 |
Lymphocytopenia [description not available] | 0 | 2.1 | 1 | 0 |
Lymphopenia Reduction in the number of lymphocytes. | 0 | 2.1 | 1 | 0 |
Cephalgia Syndromes [description not available] | 0 | 4.13 | 3 | 0 |
Headache Disorders Various conditions with the symptom of HEADACHE. Headache disorders are classified into major groups, such as PRIMARY HEADACHE DISORDERS (based on characteristics of their headache symptoms) and SECONDARY HEADACHE DISORDERS (based on their etiologies). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 4.13 | 3 | 0 |
Budd-Chiari Syndrome A condition in which the hepatic venous outflow is obstructed anywhere from the small HEPATIC VEINS to the junction of the INFERIOR VENA CAVA and the RIGHT ATRIUM. Usually the blockage is extrahepatic and caused by blood clots (THROMBUS) or fibrous webs. Parenchymal FIBROSIS is uncommon. | 0 | 8.86 | 4 | 0 |
Angiomyolipoma A benign tumor containing vascular, adipose, and muscle elements. It occurs most often in the kidney with smooth muscle elements (angiolipoleiomyoma) in association with tuberous sclerosis. (Dorland, 27th ed) | 0 | 2.43 | 2 | 0 |
Fibromatosis [description not available] | 0 | 4.18 | 6 | 0 |
Fibroma A benign tumor of fibrous or fully developed connective tissue. | 0 | 4.18 | 6 | 0 |
Bimalleolar Ankle Fractures [description not available] | 0 | 2.1 | 1 | 0 |
Ankle Fractures Fractures of any of the bones of the ANKLE. | 0 | 2.1 | 1 | 0 |
Auricular Cancer [description not available] | 0 | 5.05 | 16 | 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 | 5.05 | 16 | 0 |
Superior Vena Cava Obstruction [description not available] | 0 | 2.1 | 1 | 0 |
Chronic Liver Failure [description not available] | 0 | 2.52 | 2 | 0 |
End Stage Liver Disease Final stage of a liver disease when the liver failure is irreversible and LIVER TRANSPLANTATION is needed. | 0 | 2.52 | 2 | 0 |
Neoplasms, Vascular [description not available] | 0 | 2.95 | 4 | 0 |
Osteolysis Dissolution of bone that particularly involves the removal or loss of calcium. | 0 | 5.25 | 4 | 1 |
Left Heart Hypoplasia Syndrome [description not available] | 0 | 4.35 | 4 | 1 |
Hypoplastic Left Heart Syndrome A condition caused by underdevelopment of the whole left half of the heart. It is characterized by hypoplasia of the left cardiac chambers (HEART ATRIUM; HEART VENTRICLE), the AORTA, the AORTIC VALVE, and the MITRAL VALVE. Severe symptoms appear in early infancy when DUCTUS ARTERIOSUS closes. | 0 | 4.35 | 4 | 1 |
Aperture Syndrome, Thoracic Outlet [description not available] | 0 | 3.64 | 3 | 0 |
Thoracic Outlet Syndrome A neurovascular syndrome associated with compression of the BRACHIAL PLEXUS; SUBCLAVIAN ARTERY; and SUBCLAVIAN VEIN at the superior thoracic outlet. This may result from a variety of anomalies such as a CERVICAL RIB, anomalous fascial bands, and abnormalities of the origin or insertion of the anterior or medial scalene muscles. Clinical features may include pain in the shoulder and neck region which radiates into the arm, PARESIS or PARALYSIS of brachial plexus innervated muscles, PARESTHESIA, loss of sensation, reduction of arterial pulses in the affected extremity, ISCHEMIA, and EDEMA. (Adams et al., Principles of Neurology, 6th ed, pp214-5). | 0 | 8.64 | 3 | 0 |
Elephant Man Disease [description not available] | 0 | 4.29 | 2 | 0 |
Proteus Syndrome Hamartoneoplastic malformation syndrome of uncertain etiology characterized by partial GIGANTISM of the hands and/or feet, asymmetry of the limbs, plantar hyperplasia, hemangiomas (HEMANGIOMA), lipomas (LIPOMA), lymphangiomas (LYMPHANGIOMA), epidermal NEVI; MACROCEPHALY; cranial HYPEROSTOSIS, and long-bone overgrowth. Joseph Merrick, the so-called elephant man, apparently suffered from Proteus syndrome and not NEUROFIBROMATOSIS, a disorder with similar characteristics. | 0 | 4.29 | 2 | 0 |
Cystic Kidney Diseases [description not available] | 0 | 6.56 | 10 | 2 |
Kidney Diseases, Cystic A heterogeneous group of hereditary and acquired disorders in which the KIDNEY contains one or more CYSTS unilaterally or bilaterally (KIDNEY, CYSTIC). | 0 | 6.56 | 10 | 2 |
Enterocele An intestinal HERNIA. | 0 | 3.01 | 1 | 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 | 3.01 | 1 | 0 |
Retinal Pigment Epithelial Detachment [description not available] | 0 | 3.11 | 5 | 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 | 3.11 | 5 | 0 |
Suffocation [description not available] | 0 | 2.1 | 1 | 0 |
Asphyxia A pathological condition caused by lack of oxygen, manifested in impending or actual cessation of life. | 0 | 2.1 | 1 | 0 |
Coronary Thrombosis Coagulation of blood in any of the CORONARY VESSELS. The presence of a blood clot (THROMBUS) often leads to MYOCARDIAL INFARCTION. | 0 | 3.15 | 5 | 0 |
Infection, Postoperative Wound [description not available] | 0 | 2.44 | 2 | 0 |
Angioleiomyoma [description not available] | 0 | 7.1 | 1 | 0 |
Aortic Diseases Pathological processes involving any part of the AORTA. | 0 | 10.86 | 32 | 4 |
Indigestion [description not available] | 0 | 3.39 | 2 | 0 |
Dyspepsia Impaired digestion, especially after eating. | 0 | 3.39 | 2 | 0 |
Acute Hemorrhagic Encephalomyelitis [description not available] | 0 | 2.49 | 2 | 0 |
Atypical Lipomatous Tumor [description not available] | 0 | 4.05 | 5 | 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 | 9.05 | 5 | 0 |
Colonic Diverticulosis [description not available] | 0 | 3.48 | 1 | 1 |
Colitis Inflammation of the COLON section of the large intestine (INTESTINE, LARGE), usually with symptoms such as DIARRHEA (often with blood and mucus), ABDOMINAL PAIN, and FEVER. | 0 | 9.37 | 4 | 1 |
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 | 4.88 | 4 | 2 |
Bone Fractures [description not available] | 0 | 6.17 | 7 | 0 |
Fractures, Bone Breaks in bones. | 0 | 6.17 | 7 | 0 |
Fungal Diseases [description not available] | 0 | 2.72 | 3 | 0 |
Mycoses Diseases caused by FUNGI. | 0 | 2.72 | 3 | 0 |
Endotoxemia A condition characterized by the presence of ENDOTOXINS in the blood. On lysis, the outer cell wall of gram-negative bacteria enters the systemic circulation and initiates a pathophysiologic cascade of pro-inflammatory mediators. | 0 | 5.01 | 15 | 0 |
Rhabdomyolysis Necrosis or disintegration of skeletal muscle often followed by myoglobinuria. | 0 | 2.11 | 1 | 0 |
Odontalgia [description not available] | 0 | 2.1 | 1 | 0 |
Toothache Pain in the adjacent areas of the teeth. | 0 | 2.1 | 1 | 0 |
Bruise [description not available] | 0 | 2.43 | 2 | 0 |
Injuries, Multiple [description not available] | 0 | 2.11 | 1 | 0 |
Blunt Injuries [description not available] | 0 | 4.5 | 5 | 1 |
Contusions Injuries resulting in hemorrhage, usually manifested in the skin. | 0 | 2.43 | 2 | 0 |
Exanthem [description not available] | 0 | 2.49 | 2 | 0 |
Exanthema Diseases in which skin eruptions or rashes are a prominent manifestation. Classically, six such diseases were described with similar rashes; they were numbered in the order in which they were reported. Only the fourth (Duke's disease), fifth (ERYTHEMA INFECTIOSUM), and sixth (EXANTHEMA SUBITUM) numeric designations survive as occasional synonyms in current terminology. | 0 | 2.49 | 2 | 0 |
Nausea An unpleasant sensation in the stomach usually accompanied by the urge to vomit. Common causes are early pregnancy, sea and motion sickness, emotional stress, intense pain, food poisoning, and various enteroviruses. | 0 | 5.41 | 5 | 3 |
Adrenal Cancer [description not available] | 0 | 6.81 | 13 | 2 |
Gangliocytoma [description not available] | 0 | 4.3 | 7 | 0 |
Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis [description not available] | 0 | 4.02 | 5 | 0 |
Candida Infection [description not available] | 0 | 2.7 | 3 | 0 |
E coli Infections [description not available] | 0 | 2.92 | 4 | 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 | 2.7 | 3 | 0 |
Escherichia coli Infections Infections with bacteria of the species ESCHERICHIA COLI. | 0 | 2.92 | 4 | 0 |
Chylothorax The presence of chyle in the thoracic cavity. (Dorland, 27th ed) | 0 | 2.1 | 1 | 0 |
Burns, Electric Burns produced by contact with electric current or from a sudden discharge of electricity. | 0 | 3.01 | 1 | 0 |
Foreign-Body Migration Migration of a foreign body from its original location to some other location in the body. | 0 | 3.01 | 1 | 0 |
Nasal Diseases [description not available] | 0 | 2.72 | 3 | 0 |
Granuloma, Plasma Cell, Orbital [description not available] | 0 | 2.47 | 2 | 0 |
Orbital Pseudotumor A nonspecific tumor-like inflammatory lesion in the ORBIT of the eye. It is usually composed of mature LYMPHOCYTES; PLASMA CELLS; MACROPHAGES; LEUKOCYTES with varying degrees of FIBROSIS. Orbital pseudotumors are often associated with inflammation of the extraocular muscles (ORBITAL MYOSITIS) or inflammation of the lacrimal glands (DACRYOADENITIS). | 0 | 2.47 | 2 | 0 |
Cancer of the Uterus [description not available] | 0 | 7.17 | 21 | 1 |
Uterine Neoplasms Tumors or cancer of the UTERUS. | 0 | 12.17 | 21 | 1 |
Carotid Artery Thrombosis Blood clot formation in any part of the CAROTID ARTERIES. This may produce CAROTID STENOSIS or occlusion of the vessel, leading to TRANSIENT ISCHEMIC ATTACK; CEREBRAL INFARCTION; or AMAUROSIS FUGAX. | 0 | 2.71 | 3 | 0 |
Carbon Tetrachloride Poisoning Poisoning that results from ingestion, injection, inhalation, or skin absorption of CARBON TETRACHLORIDE. | 0 | 2.45 | 2 | 0 |
Parotiditis [description not available] | 0 | 2.69 | 3 | 0 |
Polyarthritis [description not available] | 0 | 3.38 | 7 | 0 |
Arthritis Acute or chronic inflammation of JOINTS. | 0 | 3.38 | 7 | 0 |
Tenosynovitis Inflammation of the synovial lining of a tendon sheath. Causes include trauma, tendon stress, bacterial disease (gonorrhea, tuberculosis), rheumatic disease, and gout. Common sites are the hand, wrist, shoulder capsule, hip capsule, hamstring muscles, and Achilles tendon. The tendon sheaths become inflamed and painful, and accumulate fluid. Joint mobility is usually reduced. | 0 | 4.52 | 5 | 1 |
Hyperlipemia [description not available] | 0 | 2.52 | 2 | 0 |
Hyperlipidemias Conditions with excess LIPIDS in the blood. | 0 | 2.52 | 2 | 0 |
Mucocele A retention cyst of the salivary gland, lacrimal sac, paranasal sinuses, appendix, or gallbladder. (Stedman, 26th ed) | 0 | 2.44 | 2 | 0 |
Acquired Autoimmune Hemolytic Anemia [description not available] | 0 | 2.11 | 1 | 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 | 2.11 | 1 | 0 |
Gouty Arthritis [description not available] | 0 | 7.11 | 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 | 2.11 | 1 | 0 |
Intestinal Diseases Pathological processes in any segment of the INTESTINE from DUODENUM to RECTUM. | 0 | 3.64 | 3 | 0 |
Uveal Neoplasms Tumors or cancer of the UVEA. | 0 | 3.25 | 6 | 0 |
Central Nervous System Toxoplasmosis [description not available] | 0 | 3.27 | 6 | 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 | 3.51 | 8 | 0 |
Toxoplasmosis, Cerebral Infections of the BRAIN caused by the protozoan TOXOPLASMA gondii that primarily arise in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES (see also AIDS-RELATED OPPORTUNISTIC INFECTIONS). The infection may involve the brain diffusely or form discrete abscesses. Clinical manifestations include SEIZURES, altered mentation, headache, focal neurologic deficits, and INTRACRANIAL HYPERTENSION. (From Joynt, Clinical Neurology, 1998, Ch27, pp41-3) | 0 | 3.27 | 6 | 0 |
Paraganglioma, Gangliocytic [description not available] | 0 | 3.11 | 5 | 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 | 3.11 | 5 | 0 |
Cognition Disorders Disorders characterized by disturbances in mental processes related to learning, thinking, reasoning, and judgment. | 0 | 3.55 | 8 | 0 |
Brain Thrombosis [description not available] | 0 | 3.15 | 5 | 0 |
Inner Ear Disease [description not available] | 0 | 3.71 | 10 | 0 |
Labyrinth Diseases Pathological processes of the inner ear (LABYRINTH) which contains the essential apparatus of hearing (COCHLEA) and balance (SEMICIRCULAR CANALS). | 0 | 3.71 | 10 | 0 |
Chediak-Higashi Syndrome A form of phagocyte bactericidal dysfunction characterized by unusual oculocutaneous albinism, high incidence of lymphoreticular neoplasms, and recurrent pyogenic infections. In many cell types, abnormal lysosomes are present leading to defective pigment distribution and abnormal neutrophil functions. The disease is transmitted by autosomal recessive inheritance and a similar disorder occurs in the beige mouse, the Aleutian mink, and albino Hereford cattle. | 0 | 2.11 | 1 | 0 |
Psychoses [description not available] | 0 | 2.11 | 1 | 0 |
Psychotic Disorders Disorders in which there is a loss of ego boundaries or a gross impairment in reality testing with delusions or prominent hallucinations. (From DSM-IV, 1994) | 0 | 2.11 | 1 | 0 |
Bladder, Overactive [description not available] | 0 | 2.11 | 1 | 0 |
Urinary Bladder, Overactive Symptom of overactive detrusor muscle of the URINARY BLADDER that contracts with abnormally high frequency and urgency. Overactive bladder is characterized by the frequent feeling of needing to urinate during the day, during the night, or both. URINARY INCONTINENCE may or may not be present. | 0 | 2.11 | 1 | 0 |
Arterial Inflammation [description not available] | 0 | 3.35 | 2 | 0 |
Dysembryoma [description not available] | 0 | 3.29 | 6 | 0 |
Teratoma A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642) | 0 | 3.29 | 6 | 0 |
Rhabdoid Tumor A rare but highly lethal childhood tumor found almost exclusively in infants. Histopathologically, it resembles RHABDOMYOSARCOMA but the tumor cells are not of myogenic origin. Although it arises primarily in the kidney, it may be found in other parts of the body. The rhabdoid cytomorphology is believed to be the expression of a very primitive malignant cell. (From Holland et al., Cancer Medicine, 3d ed, p2210) | 0 | 2.78 | 3 | 0 |
Diabetic Glomerulosclerosis [description not available] | 0 | 4.83 | 7 | 0 |
Hyperpotassemia [description not available] | 0 | 3.87 | 2 | 0 |
Anemia A reduction in the number of circulating ERYTHROCYTES or in the quantity of HEMOGLOBIN. | 0 | 3.37 | 2 | 0 |
Diabetic Nephropathies KIDNEY injuries associated with diabetes mellitus and affecting KIDNEY GLOMERULUS; ARTERIOLES; KIDNEY TUBULES; and the interstitium. Clinical signs include persistent PROTEINURIA, from microalbuminuria progressing to ALBUMINURIA of greater than 300 mg/24 h, leading to reduced GLOMERULAR FILTRATION RATE and END-STAGE RENAL DISEASE. | 0 | 4.83 | 7 | 0 |
Hyperkalemia Abnormally high potassium concentration in the blood, most often due to defective renal excretion. It is characterized clinically by electrocardiographic abnormalities (elevated T waves and depressed P waves, and eventually by atrial asystole). In severe cases, weakness and flaccid paralysis may occur. (Dorland, 27th ed) | 0 | 3.87 | 2 | 0 |
Chondromatosis, Synovial Rare, benign, chronic, progressive metaplasia in which cartilage is formed in the synovial membranes of joints, tendon sheaths, or bursae. Some of the metaplastic foci can become detached producing loose bodies. When the loose bodies undergo secondary calcification, the condition is called synovial osteochondromatosis. | 0 | 2.76 | 3 | 0 |
Deficiency, Vitamin D [description not available] | 0 | 2.11 | 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 | 2.11 | 1 | 0 |
Chronic Hepatitis C [description not available] | 0 | 3.67 | 3 | 0 |
Thalassemias [description not available] | 0 | 2.11 | 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 | 7.11 | 1 | 0 |
Hepatitis C, Chronic INFLAMMATION of the LIVER in humans that is caused by HEPATITIS C VIRUS lasting six months or more. Chronic hepatitis C can lead to LIVER CIRRHOSIS. | 0 | 3.67 | 3 | 0 |
Pulmonary Stenoses [description not available] | 0 | 2.53 | 2 | 0 |
Dyskinesia Syndromes [description not available] | 0 | 2.11 | 1 | 0 |
Action Tremor [description not available] | 0 | 3.65 | 3 | 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 | 2.11 | 1 | 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 | 3.65 | 3 | 0 |
Chemical and Drug Induced Liver Injury, Chronic Liver disease lasting six months or more, caused by an adverse effect of a drug or chemical. The adverse effect may be caused by drugs, drug metabolites, chemicals from the environment, or an idiosyncratic response. | 0 | 2.13 | 1 | 0 |
Cerebellar Diseases Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA. | 0 | 5.78 | 15 | 0 |
Cancer of Testis [description not available] | 0 | 2.44 | 2 | 0 |
Testicular Neoplasms Tumors or cancer of the TESTIS. Germ cell tumors (GERMINOMA) of the testis constitute 95% of all testicular neoplasms. | 0 | 2.44 | 2 | 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 | 3.29 | 6 | 0 |
Angiosarcoma [description not available] | 0 | 3.86 | 12 | 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 | 3.86 | 12 | 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 | 2.43 | 2 | 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 | 4.19 | 6 | 0 |
Brugada ECG Pattern [description not available] | 0 | 2.13 | 1 | 0 |
Brugada Syndrome An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit. | 0 | 2.13 | 1 | 0 |
Hemorrhagic Shock [description not available] | 0 | 2.44 | 2 | 0 |
Abscess, Tubercular, Intracranial [description not available] | 0 | 2.42 | 2 | 0 |
Health Care Associated Infection [description not available] | 0 | 2.11 | 1 | 0 |
Acute Post-operative Pain [description not available] | 0 | 14.82 | 677 | 0 |
Cross Infection Any infection which a patient contracts in a health-care institution. | 0 | 2.11 | 1 | 0 |
Pain, Postoperative Pain during the period after surgery. | 0 | 14.82 | 677 | 0 |
Schistosoma japonicum Infection [description not available] | 0 | 2.49 | 2 | 0 |
Neoplasms, Nerve Sheath [description not available] | 0 | 4.21 | 6 | 0 |
Nerve Sheath Neoplasms Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category. | 0 | 4.21 | 6 | 0 |
Calciphylaxes [description not available] | 0 | 3.39 | 2 | 0 |
Nail Diseases Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. | 0 | 3.62 | 3 | 0 |
Itching [description not available] | 0 | 3.41 | 2 | 0 |
Bullous Dermatoses [description not available] | 0 | 3.03 | 1 | 0 |
Incontinentia Pigmenti Achromians [description not available] | 0 | 3.03 | 1 | 0 |
Pruritus An intense itching sensation that produces the urge to rub or scratch the skin to obtain relief. | 0 | 3.41 | 2 | 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 | 6.14 | 6 | 2 |
Crow-Fukase Syndrome [description not available] | 0 | 2.11 | 1 | 0 |
POEMS Syndrome A multisystemic disorder characterized by a sensorimotor polyneuropathy (POLYNEUROPATHIES), organomegaly, endocrinopathy, monoclonal gammopathy, and pigmentary skin changes. Other clinical features which may be present include EDEMA; CACHEXIA; microangiopathic glomerulopathy; pulmonary hypertension (HYPERTENSION, PULMONARY); cutaneous necrosis; THROMBOCYTOSIS; and POLYCYTHEMIA. This disorder is frequently associated with osteosclerotic myeloma. (From Adams et al., Principles of Neurology, 6th ed, p1335; Rev Med Interne 1997;18(7):553-62) | 0 | 2.11 | 1 | 0 |
Emesis, Postoperative [description not available] | 0 | 4.15 | 3 | 1 |
Choked Disk [description not available] | 0 | 3.1 | 5 | 0 |
Benign Intracranial Hypertension [description not available] | 0 | 4.32 | 7 | 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 | 3.1 | 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 | 4.32 | 7 | 0 |
Postoperative Nausea and Vomiting Emesis and queasiness occurring after anesthesia. | 0 | 4.15 | 3 | 1 |
Cold Injury A physical injury caused by exposure of the body to extremely low ambient temperatures that may lead to loss of body parts, or in extreme cases, death. Examples of cold injury are FROSTBITE and CHILBLAINS. | 0 | 2.13 | 1 | 0 |
Acid Aspiration Syndrome [description not available] | 0 | 3.03 | 1 | 0 |
Pneumonia, Aspiration A type of lung inflammation resulting from the aspiration of food, liquid, or gastric contents into the upper RESPIRATORY TRACT. | 0 | 3.03 | 1 | 0 |
Craniomandibular Diseases [description not available] | 0 | 2.13 | 1 | 0 |
Response Evaluation Criteria in Solid Tumors An internationally recognized set of published rules used for evaluation of cancer treatment that define when tumors found in cancer patients improve, worsen, or remain stable during treatment. These criteria are based specifically on the response of the tumor(s) to treatment, and not on the overall health status of the patient resulting from treatment. | 0 | 2.13 | 1 | 0 |
Abdominal Neoplasms New abnormal growth of tissue in the ABDOMEN. | 0 | 9.88 | 18 | 3 |
Cardiac Rupture, Post-Infarction [description not available] | 0 | 2.95 | 4 | 0 |
Endothelioma, Vascular [description not available] | 0 | 4.51 | 5 | 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 | 9.51 | 5 | 0 |
Anomalous Pulmonary Venous Return [description not available] | 0 | 2.44 | 2 | 0 |
Glomangioma [description not available] | 0 | 3.26 | 6 | 0 |
Double Outlet Right Ventricle Incomplete transposition of the great vessels in which both the AORTA and the PULMONARY ARTERY arise from the RIGHT VENTRICLE. The only outlet of the LEFT VENTRICLE is a large ventricular septal defect (VENTRICULAR SEPTAL DEFECTS or VSD). The various subtypes are classified by the location of the septal defect, such as subaortic, subpulmonary, or noncommitted. | 0 | 2.13 | 1 | 0 |
Cardiac Septal Defect [description not available] | 0 | 2.13 | 1 | 0 |
Essential Polyarteritis [description not available] | 0 | 3.38 | 2 | 0 |
Abdomen, Acute A clinical syndrome with acute abdominal pain that is severe, localized, and rapid in onset. Acute abdomen may be caused by a variety of disorders, injuries, or diseases. | 0 | 3.89 | 4 | 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 | 2.42 | 2 | 0 |
Diathesis [description not available] | 0 | 4.16 | 3 | 1 |
Central Nervous System Cysticercosis [description not available] | 0 | 5.94 | 9 | 1 |
Neurocysticercosis Infection of the brain, spinal cord, or perimeningeal structures with the larval forms of the genus TAENIA (primarily T. solium in humans). Lesions formed by the organism are referred to as cysticerci. The infection may be subacute or chronic, and the severity of symptoms depends on the severity of the host immune response and the location and number of lesions. SEIZURES represent the most common clinical manifestation although focal neurologic deficits may occur. (From Joynt, Clinical Neurology, 1998, Ch27, pp46-50) | 0 | 5.94 | 9 | 1 |
Sarcoma 180 An experimental sarcoma of mice. | 0 | 2.13 | 1 | 0 |
Carcinoma, Ehrlich Tumor A transplantable, poorly differentiated malignant tumor which appeared originally as a spontaneous breast carcinoma in a mouse. It grows in both solid and ascitic forms. | 0 | 3.28 | 6 | 0 |
Emergencies Situations or conditions requiring immediate intervention to avoid serious adverse results. | 0 | 2.73 | 3 | 0 |
Contracture Prolonged shortening of the muscle or other soft tissue around a joint, preventing movement of the joint. | 0 | 3.68 | 3 | 0 |
Agenesis of Hemidiaphragm [description not available] | 0 | 2.13 | 1 | 0 |
Embryopathies [description not available] | 0 | 2.13 | 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 | 2.13 | 1 | 0 |
Blastomyces brasiliensis Infection [description not available] | 0 | 2.13 | 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 | 4.12 | 3 | 0 |
Orbital Neoplasms Neoplasms of the bony orbit and contents except the eyeball. | 0 | 5.53 | 16 | 0 |
Fibrous Histiocytoma of Tendon Sheath [description not available] | 0 | 2.13 | 1 | 0 |
Giant Cell Tumor of Tendon Sheath A tumor arising in the SYNOVIAL MEMBRANE; SYNOVIAL BURSA; or TENDON sheath. It is characterized by OSTEOCLAST-like GIANT CELLS; FOAM CELLS; pigmented HEMOSIDERIN-laden MACROPHAGES and inflammatory infiltrate. It is classified either as diffuse or localized tenosynovitis. | 0 | 2.13 | 1 | 0 |
Cholangiocellular Carcinoma [description not available] | 0 | 7.62 | 9 | 3 |
Bile Duct Cancer [description not available] | 0 | 7.36 | 10 | 2 |
Bile Duct Neoplasms Tumors or cancer of the BILE DUCTS. | 0 | 7.36 | 10 | 2 |
Cholangiocarcinoma A malignant tumor arising from the epithelium of the BILE DUCTS. | 0 | 12.62 | 9 | 3 |
Neuroendocrine Tumors Tumors whose cells possess secretory granules and originate from the neuroectoderm, i.e., the cells of the ectoblast or epiblast that program the neuroendocrine system. Common properties across most neuroendocrine tumors include ectopic hormone production (often via APUD CELLS), the presence of tumor-associated antigens, and isozyme composition. | 0 | 9.65 | 6 | 0 |
Autosomal Dominant Juvenile Parkinson Disease [description not available] | 0 | 2.13 | 1 | 0 |
Parkinsonian Disorders A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA. | 0 | 2.13 | 1 | 0 |
Fibrosis, Radiation [description not available] | 0 | 2.13 | 1 | 0 |
Congenital Epulides [description not available] | 0 | 2.13 | 1 | 0 |
Mandibular Neoplasms Tumors or cancer of the MANDIBLE. | 0 | 3.15 | 5 | 0 |
Cachexia General ill health, malnutrition, and weight loss, usually associated with chronic disease. | 0 | 2.13 | 1 | 0 |
Radiation Pneumonitis Inflammation of the lung due to harmful effects of ionizing or non-ionizing radiation. | 0 | 2.13 | 1 | 0 |
Athletic Injuries Injuries incurred during participation in competitive or non-competitive sports. | 0 | 7.94 | 4 | 0 |
Bone Stress Reaction [description not available] | 0 | 2.44 | 2 | 0 |
Dyslipidemia [description not available] | 0 | 2.13 | 1 | 0 |
Dyslipidemias Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL, high TRIGLYCERIDES, low HIGH DENSITY LIPOPROTEIN CHOLESTEROL, and elevated LOW DENSITY LIPOPROTEIN CHOLESTEROL. | 0 | 2.13 | 1 | 0 |
Chronic Lung Injury [description not available] | 0 | 2.15 | 1 | 0 |
Respiration Disorders Diseases of the respiratory system in general or unspecified or for a specific respiratory disease not available. | 0 | 2.44 | 2 | 0 |
Aspergillus Infection [description not available] | 0 | 2.49 | 2 | 0 |
Aspergillosis Infections with fungi of the genus ASPERGILLUS. | 0 | 2.49 | 2 | 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 | 2.43 | 2 | 0 |
Earache Pain in the ear. | 0 | 2.15 | 1 | 0 |
Encephalopathy, Traumatic [description not available] | 0 | 2.13 | 1 | 0 |
Brain Injuries, Traumatic A form of acquired brain injury which occurs when a sudden trauma causes damage to the brain. | 0 | 2.13 | 1 | 0 |
Enlarged Liver [description not available] | 0 | 2.15 | 1 | 0 |
Meningitis, Tuberculous [description not available] | 0 | 2.91 | 4 | 0 |
Tuberculosis, Meningeal A form of bacterial meningitis caused by MYCOBACTERIUM TUBERCULOSIS or rarely MYCOBACTERIUM BOVIS. The organism seeds the meninges and forms microtuberculomas which subsequently rupture. The clinical course tends to be subacute, with progressions occurring over a period of several days or longer. Headache and meningeal irritation may be followed by SEIZURES, cranial neuropathies, focal neurologic deficits, somnolence, and eventually COMA. The illness may occur in immunocompetent individuals or as an OPPORTUNISTIC INFECTION in the ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunodeficiency syndromes. (From Adams et al., Principles of Neurology, 6th ed, pp717-9) | 0 | 2.91 | 4 | 0 |
Nephrolithiasis Formation of stones in the KIDNEY. | 0 | 2.13 | 1 | 0 |
Thrombopenia [description not available] | 0 | 2.73 | 3 | 0 |
Thrombocytopenia A subnormal level of BLOOD PLATELETS. | 0 | 7.73 | 3 | 0 |
Acute Pain Intensely discomforting, distressful, or agonizing sensation associated with trauma or disease, with well-defined location, character, and timing. | 0 | 2.15 | 1 | 0 |
Lung Adenocarcinoma [description not available] | 0 | 2.15 | 1 | 0 |
Adenocarcinoma of Lung A carcinoma originating in the lung and the most common lung cancer type in never-smokers. Malignant cells exhibit distinct features such as glandular epithelial, or tubular morphology. Mutations in KRAS, EGFR, BRAF, and ERBB2 genes are associated with this cancer. | 0 | 2.15 | 1 | 0 |
Arsenic Encephalopathy [description not available] | 0 | 2.15 | 1 | 0 |
Beuren Syndrome [description not available] | 0 | 2.15 | 1 | 0 |
Aortic Stenosis, Supravalvular A pathological constriction occurring in the region above the AORTIC VALVE. It is characterized by restricted outflow from the LEFT VENTRICLE into the AORTA. | 0 | 2.15 | 1 | 0 |
Acute Onset Aura Migraine [description not available] | 0 | 2.94 | 4 | 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 | 2.94 | 4 | 0 |
Metabolic Acidosis [description not available] | 0 | 6 | 5 | 0 |
Acidosis A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up. | 0 | 6 | 5 | 0 |
Jaundice, Cholestatic [description not available] | 0 | 3.38 | 2 | 0 |
Jaundice, Obstructive Jaundice, the condition with yellowish staining of the skin and mucous membranes, that is due to impaired BILE flow in the BILIARY TRACT, such as INTRAHEPATIC CHOLESTASIS, or EXTRAHEPATIC CHOLESTASIS. | 0 | 3.38 | 2 | 0 |
Intraventricular Septal Defects [description not available] | 0 | 2.71 | 3 | 0 |
Atresia, Pulmonary [description not available] | 0 | 4.55 | 3 | 0 |
Heart Septal Defects, Ventricular Developmental abnormalities in any portion of the VENTRICULAR SEPTUM resulting in abnormal communications between the two lower chambers of the heart. Classification of ventricular septal defects is based on location of the communication, such as perimembranous, inlet, outlet (infundibular), central muscular, marginal muscular, or apical muscular defect. | 0 | 2.71 | 3 | 0 |
Osteoid Osteoma [description not available] | 0 | 3.4 | 7 | 0 |
Cancer of Spleen [description not available] | 0 | 3.38 | 7 | 0 |
Angioma, Sclerosing [description not available] | 0 | 2.41 | 2 | 0 |
Histiocytoma, Benign Fibrous A benign tumor composed, wholly or in part, of cells with the morphologic characteristics of HISTIOCYTES and with various fibroblastic components. Fibrous histiocytomas can occur anywhere in the body. When they occur in the skin, they are called dermatofibromas or sclerosing hemangiomas. (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 5th ed, p1747) | 0 | 2.41 | 2 | 0 |
Facial Dermatoses Skin diseases involving the FACE. | 0 | 2.44 | 2 | 0 |
Ovarian Diseases Pathological processes of the OVARY. | 0 | 2.91 | 4 | 0 |
Pelvic Pain Pain in the pelvic region of genital and non-genital origin. | 0 | 3.81 | 2 | 1 |
Puerperal Disorders Disorders or diseases associated with PUERPERIUM, the six-to-eight-week period immediately after PARTURITION in humans. | 0 | 4.04 | 5 | 0 |
Abdominal Cramps [description not available] | 0 | 2.96 | 1 | 0 |
Abnormalities, Radiation-Induced Congenital changes in the morphology of organs produced by exposure to ionizing or non-ionizing radiation. | 0 | 2.96 | 1 | 0 |
Cephalopelvic Disproportion A condition in which the HEAD of the FETUS is larger than the mother's PELVIS through which the fetal head must pass during a vaginal delivery. | 0 | 2.96 | 1 | 0 |
Autoimmune Diabetes [description not available] | 0 | 2.43 | 2 | 0 |
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 | 2.43 | 2 | 0 |
MODS [description not available] | 0 | 2.92 | 4 | 0 |
Multiple Organ Failure A progressive condition usually characterized by combined failure of several organs such as the lungs, liver, kidney, along with some clotting mechanisms, usually postinjury or postoperative. | 0 | 2.92 | 4 | 0 |
Endothelioma, Lymphatic [description not available] | 0 | 3.51 | 8 | 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 | 8.51 | 8 | 0 |
Biliary Calculi [description not available] | 0 | 2.71 | 3 | 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 | 2.71 | 3 | 0 |
Ptosis, Eyelid [description not available] | 0 | 2.41 | 2 | 0 |
Blepharoptosis Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle. | 0 | 2.41 | 2 | 0 |
Orthopedic Disorders [description not available] | 0 | 5.32 | 7 | 0 |
Musculoskeletal Diseases Diseases of the muscles and their associated ligaments and other connective tissue and of the bones and cartilage viewed collectively. | 0 | 5.32 | 7 | 0 |
Giant Osteoid Osteoma [description not available] | 0 | 2.04 | 1 | 0 |
B. burgdorferi Infection [description not available] | 0 | 2.92 | 4 | 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 | 7.92 | 4 | 0 |
Ureteral Diseases Pathological processes involving the URETERS. | 0 | 2.42 | 2 | 0 |
Follicle Stimulating Hormone, Inappropriate Secretion [description not available] | 0 | 2.05 | 1 | 0 |
Muscular Dystrophy, Animal MUSCULAR DYSTROPHY that occurs in VERTEBRATE animals. | 0 | 3.25 | 6 | 0 |
Alcohol Drinking Behaviors associated with the ingesting of ALCOHOLIC BEVERAGES, including social drinking. | 0 | 2.05 | 1 | 0 |
Eye Disorders [description not available] | 0 | 4.88 | 8 | 0 |
Eye Diseases Diseases affecting the eye. | 0 | 4.88 | 8 | 0 |
Vesicoureteral Reflux [description not available] | 0 | 2.44 | 2 | 0 |
Ureterocele A cystic dilatation of the end of a URETER as it enters into the URINARY BLADDER. It is characterized by the ballooning of the ureteral orifice into the lumen of the bladder and may obstruct urine flow. | 0 | 2.05 | 1 | 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 | 2.44 | 2 | 0 |
Hypermelanosis [description not available] | 0 | 3.85 | 2 | 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 | 3.85 | 2 | 0 |
Diabetic Angiopathies VASCULAR DISEASES that are associated with DIABETES MELLITUS. | 0 | 2.04 | 1 | 0 |
Gangrene Death and putrefaction of tissue usually due to a loss of blood supply. | 0 | 2.04 | 1 | 0 |
Elevated ICP (Intracranial Pressure) [description not available] | 0 | 2.44 | 2 | 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 | 2.44 | 2 | 0 |
Secondary Hyperparathyroidism [description not available] | 0 | 2.96 | 1 | 0 |
CKD-MBD [description not available] | 0 | 3.59 | 3 | 0 |
Rheumatism [description not available] | 0 | 2.96 | 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 | 2.96 | 1 | 0 |
Chronic Kidney Disease-Mineral and Bone Disorder Decalcification of bone or abnormal bone development due to chronic KIDNEY DISEASES, in which 1,25-DIHYDROXYVITAMIN D3 synthesis by the kidneys is impaired, leading to reduced negative feedback on PARATHYROID HORMONE. The resulting SECONDARY HYPERPARATHYROIDISM eventually leads to bone disorders. | 0 | 3.59 | 3 | 0 |
Rheumatic Diseases Disorders of connective tissue, especially the joints and related structures, characterized by inflammation, degeneration, or metabolic derangement. | 0 | 2.96 | 1 | 0 |
Peritoneal Diseases Pathological processes involving the PERITONEUM. | 0 | 3.84 | 4 | 0 |
Cancer, Embryonal [description not available] | 0 | 3.12 | 5 | 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 | 3.12 | 5 | 0 |
Adenoma, Prostatic [description not available] | 0 | 5.34 | 7 | 2 |
Prostatic Hyperplasia Increase in constituent cells in the PROSTATE, leading to enlargement of the organ (hypertrophy) and adverse impact on the lower urinary tract function. This can be caused by increased rate of cell proliferation, reduced rate of cell death, or both. | 0 | 5.34 | 7 | 2 |
Dancing Eyes-Dancing Feet Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Opsoclonus-Myoclonus Syndrome A neurological condition that is characterized by uncontrolled rapid irregular movements of the eye (OPSOCLONUS) and the muscle (MYOCLONUS) causing unsteady, trembling gait. It is also known as dancing eyes-dancing feet syndrome and is often associated with neoplasms, viral infections, or autoimmune disorders involving the nervous system. | 0 | 2.05 | 1 | 0 |
Complex Regional Pain Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Complex Regional Pain Syndromes Conditions characterized by pain involving an extremity or other body region, HYPERESTHESIA, and localized autonomic dysfunction following injury to soft tissue or nerve. The pain is usually associated with ERYTHEMA; SKIN TEMPERATURE changes, abnormal sudomotor activity (i.e., changes in sweating due to altered sympathetic innervation) or edema. The degree of pain and other manifestations is out of proportion to that expected from the inciting event. Two subtypes of this condition have been described: type I; (REFLEX SYMPATHETIC DYSTROPHY) and type II; (CAUSALGIA). (From Pain 1995 Oct;63(1):127-33) | 0 | 2.05 | 1 | 0 |
Keratocysts [description not available] | 0 | 2.73 | 3 | 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 | 2.46 | 2 | 0 |
Mandibular Diseases Diseases involving the MANDIBLE. | 0 | 4.52 | 5 | 1 |
Altered Level of Consciousness [description not available] | 0 | 2.72 | 3 | 0 |
Cancer of the Vagina [description not available] | 0 | 2.05 | 1 | 0 |
Vaginal Neoplasms Tumors or cancer of the VAGINA. | 0 | 2.05 | 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 | 2.05 | 1 | 0 |
Glenohumeral Dislocation [description not available] | 0 | 2.7 | 3 | 0 |
Hemangioendothelioma, Epithelioid A tumor of medium-to-large veins, composed of plump-to-spindled endothelial cells that bulge into vascular spaces in a tombstone-like fashion. These tumors are thought to have borderline aggression, where one-third develop local recurrences, but only rarely metastasize. It is unclear whether the epithelioid hemangioendothelioma is truly neoplastic or an exuberant tissue reaction, nor is it clear if this is equivalent to Kimura's disease (see ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA). (Segen, Dictionary of Modern Medicine, 1992) | 0 | 2.44 | 2 | 0 |
Rib Fractures Fractures of any of the RIBS. | 0 | 2.05 | 1 | 0 |
Cancer of Pelvis [description not available] | 0 | 8.81 | 14 | 2 |
ADPKD [description not available] | 0 | 8.12 | 5 | 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 | 3.12 | 5 | 0 |
Lassitude [description not available] | 0 | 5.27 | 4 | 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 | 5.27 | 4 | 1 |
Chronic Hepatitis [description not available] | 0 | 3.35 | 2 | 0 |
Hepatitis, Chronic INFLAMMATION of the LIVER with ongoing hepatocellular injury for 6 months or more, characterized by NECROSIS of HEPATOCYTES and inflammatory cell (LEUKOCYTES) infiltration. Chronic hepatitis can be caused by viruses, medications, autoimmune diseases, and other unknown factors. | 0 | 3.35 | 2 | 0 |
Brucella Infection [description not available] | 0 | 2.05 | 1 | 0 |
Central Nervous System Infection [description not available] | 0 | 2.05 | 1 | 0 |
Brucellosis Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss. | 0 | 2.05 | 1 | 0 |
Malignant Fibrohistiocytic Tumors [description not available] | 0 | 2.43 | 2 | 0 |
Histiocytoma, Malignant Fibrous The most commonly diagnosed soft tissue sarcoma. It is a neoplasm with a fibrohistiocytic appearance found chiefly in later adult life, with peak incidence in the 7th decade. | 0 | 2.43 | 2 | 0 |
Breast Diseases Pathological processes of the BREAST. | 0 | 5.73 | 20 | 0 |
Carcinoma, Intraepithelial [description not available] | 0 | 4.77 | 7 | 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 | 4.77 | 7 | 0 |
Cancer of Mouth [description not available] | 0 | 5.09 | 10 | 0 |
Mouth Neoplasms Tumors or cancer of the MOUTH. | 0 | 5.09 | 10 | 0 |
Hemangioma, Capillary A dull red, firm, dome-shaped hemangioma, sharply demarcated from surrounding skin, usually located on the head and neck, which grows rapidly and generally undergoes regression and involution without scarring. It is caused by proliferation of immature capillary vessels in active stroma, and is usually present at birth or occurs within the first two or three months of life. (Dorland, 27th ed) | 0 | 3.65 | 3 | 0 |
Bilateral Nasal Obstruction [description not available] | 0 | 2.95 | 4 | 0 |
Hemangiopericytoma A tumor composed of spindle cells with a rich vascular network, which apparently arises from pericytes, cells of smooth muscle origin that lie around small vessels. Benign and malignant hemangiopericytomas exist, and the rarity of these lesions has led to considerable confusion in distinguishing between benign and malignant variants. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1364) | 0 | 2.71 | 3 | 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. | 0 | 2.95 | 4 | 0 |
Wallerian Degeneration Degeneration of distal aspects of a nerve axon following injury to the cell body or proximal portion of the axon. The process is characterized by fragmentation of the axon and its MYELIN SHEATH. | 0 | 2.44 | 2 | 0 |
Basilar Steal Syndrome [description not available] | 0 | 2.95 | 4 | 0 |
Bile Duct Obstruction, Intrahepatic [description not available] | 0 | 2.41 | 2 | 0 |
Cholestasis, Intrahepatic Impairment of bile flow due to injury to the HEPATOCYTES; BILE CANALICULI; or the intrahepatic bile ducts (BILE DUCTS, INTRAHEPATIC). | 0 | 2.41 | 2 | 0 |
Mycoplasma dispar Infection [description not available] | 0 | 2.05 | 1 | 0 |
Jaw Diseases Diseases involving the JAW. | 0 | 3.8 | 2 | 1 |
Maxillary Diseases Diseases involving the MAXILLA. | 0 | 4.72 | 2 | 1 |
Cartilage Fractures [description not available] | 0 | 3.33 | 2 | 0 |
Aesthesioneuroblastoma [description not available] | 0 | 2.05 | 1 | 0 |
Esthesioneuroblastoma, Olfactory A malignant olfactory neuroblastoma arising from the olfactory epithelium of the superior nasal cavity and cribriform plate. It is uncommon (3% of nasal tumors) and rarely is associated with the production of excess hormones (e.g., SIADH, Cushing Syndrome). It has a high propensity for multiple local recurrences and bony metastases. (From Holland et al., Cancer Medicine, 3rd ed, p1245; J Laryngol Otol 1998 Jul;112(7):628-33) | 0 | 2.05 | 1 | 0 |
Acquired Immune Deficiency Syndrome [description not available] | 0 | 2.92 | 4 | 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 | 2.92 | 4 | 0 |
Spider Veins [description not available] | 0 | 2.7 | 3 | 0 |
Neovascularization, Optic Disc [description not available] | 0 | 2.42 | 2 | 0 |
Telangiectasis Permanent dilation of preexisting blood vessels (CAPILLARIES; ARTERIOLES; VENULES) creating small focal red lesions, most commonly in the skin or mucous membranes. It is characterized by the prominence of skin blood vessels, such as vascular spiders. | 0 | 2.7 | 3 | 0 |
Retinal Neovascularization Formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina. | 0 | 2.42 | 2 | 0 |
Choroid Plexus Neoplasms, Primary [description not available] | 0 | 5.23 | 4 | 1 |
Choroid Plexus Neoplasms Benign or malignant tumors which arise from the choroid plexus of the ventricles of the brain. Papillomas (see PAPILLOMA, CHOROID PLEXUS) and carcinomas are the most common histologic subtypes, and tend to seed throughout the ventricular and subarachnoid spaces. Clinical features include headaches, ataxia and alterations of consciousness, primarily resulting from associated HYDROCEPHALUS. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2072; J Neurosurg 1998 Mar;88(3):521-8) | 0 | 5.23 | 4 | 1 |
Esophageal Varices [description not available] | 0 | 7.43 | 2 | 0 |
Esophageal and Gastric Varices Dilated blood vessels in the ESOPHAGUS or GASTRIC FUNDUS that shunt blood from the portal circulation (PORTAL SYSTEM) to the systemic venous circulation. Often they are observed in individuals with portal hypertension (HYPERTENSION, PORTAL). | 0 | 2.43 | 2 | 0 |
Atypical Cluster Headache [description not available] | 0 | 2.05 | 1 | 0 |
Diabetic Feet [description not available] | 0 | 2.69 | 3 | 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 | 2.69 | 3 | 0 |
Cough A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. It is a protective response that serves to clear the trachea, bronchi, and/or lungs of irritants and secretions, or to prevent aspiration of foreign materials into the lungs. | 0 | 2.46 | 2 | 0 |
Daytime Sleepiness [description not available] | 0 | 2.05 | 1 | 0 |
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 | 2.05 | 1 | 0 |
Angor Pectoris [description not available] | 0 | 4.34 | 4 | 1 |
Angina Pectoris The symptom of paroxysmal pain consequent to MYOCARDIAL ISCHEMIA usually of distinctive character, location and radiation. It is thought to be provoked by a transient stressful situation during which the oxygen requirements of the MYOCARDIUM exceed that supplied by the CORONARY CIRCULATION. | 0 | 4.34 | 4 | 1 |
Mesothelioma A tumor derived from mesothelial tissue (peritoneum, pleura, pericardium). It appears as broad sheets of cells, with some regions containing spindle-shaped, sarcoma-like cells and other regions showing adenomatous patterns. Pleural mesotheliomas have been linked to exposure to asbestos. (Dorland, 27th ed) | 0 | 3.87 | 4 | 0 |
Eosinophilia, Tropical [description not available] | 0 | 2.46 | 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 | 2.44 | 2 | 0 |
Eosinophilia Abnormal increase of EOSINOPHILS in the blood, tissues or organs. | 0 | 2.46 | 2 | 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 | 2.05 | 1 | 0 |
Chloasma [description not available] | 0 | 3.32 | 2 | 0 |
Mole, Skin [description not available] | 0 | 2.05 | 1 | 0 |
Neurocutaneous Disorders [description not available] | 0 | 4.57 | 3 | 0 |
Melanosis Disorders of increased melanin pigmentation that develop without preceding inflammatory disease. | 0 | 3.32 | 2 | 0 |
Carcinoma, Adenosquamous A mixed adenocarcinoma and squamous cell or epidermoid carcinoma. | 0 | 5.41 | 5 | 1 |
Cancer of Endometrium [description not available] | 0 | 5.65 | 10 | 2 |
Endometrial Neoplasms Tumors or cancer of ENDOMETRIUM, the mucous lining of the UTERUS. These neoplasms can be benign or malignant. Their classification and grading are based on the various cell types and the percent of undifferentiated cells. | 0 | 5.65 | 10 | 2 |
Hemoglobinopathies A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. | 0 | 8.43 | 1 | 1 |
Cancer of Penis [description not available] | 0 | 2.44 | 2 | 0 |
Penile Neoplasms Cancers or tumors of the PENIS or of its component tissues. | 0 | 2.44 | 2 | 0 |
Congestive Ophthalmopathy [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 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 | 2.05 | 1 | 0 |
Aspergillosis, Nervous System Invasive [description not available] | 0 | 2.05 | 1 | 0 |
Neuroaspergillosis Infections of the nervous system caused by fungi of the genus ASPERGILLUS, most commonly ASPERGILLUS FUMIGATUS. Aspergillus infections may occur in immunocompetent hosts, but are more prevalent in individuals with IMMUNOLOGIC DEFICIENCY SYNDROMES. The organism may spread to the nervous system from focal infections in the lung, mastoid region, sinuses, inner ear, bones, eyes, gastrointestinal tract, and heart. Sinus infections may be locally invasive and enter the intracranial compartment, producing MENINGITIS, FUNGAL; cranial neuropathies; and abscesses in the frontal lobes of the brain. (From Joynt, Clinical Neurology, 1998, Ch 27, pp62-3) | 0 | 2.05 | 1 | 0 |
Alveolar Echinococcosis, Hepatic [description not available] | 0 | 2.42 | 2 | 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 | 4.52 | 9 | 0 |
Epidural Neoplasm, Malignant [description not available] | 0 | 3.83 | 4 | 0 |
Angiogranuloma [description not available] | 0 | 2.05 | 1 | 0 |
Scoliosis An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) | 0 | 3.62 | 3 | 0 |
Atypical Ductal Hyperplasia [description not available] | 0 | 5.25 | 7 | 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 | 5.25 | 7 | 0 |
Acute Necrotizing Pancreatitis [description not available] | 0 | 7.72 | 3 | 0 |
Alcoholic Pancreatitis [description not available] | 0 | 7.05 | 1 | 0 |
Caries, Dental [description not available] | 0 | 2.41 | 2 | 0 |
Dental Deposit [description not available] | 0 | 2.05 | 1 | 0 |
Dental Caries Localized destruction of the tooth surface initiated by decalcification of the enamel followed by enzymatic lysis of organic structures and leading to cavity formation. If left unchecked, the cavity may penetrate the enamel and dentin and reach the pulp. | 0 | 2.41 | 2 | 0 |
Hepatitis INFLAMMATION of the LIVER. | 0 | 9.99 | 9 | 0 |
Hypovolemic [description not available] | 0 | 2.05 | 1 | 0 |
Hypovolemia An abnormally low volume of blood circulating through the body. It may result in hypovolemic shock (see SHOCK). | 0 | 2.05 | 1 | 0 |
Fasciola Infection [description not available] | 0 | 2.05 | 1 | 0 |
Asthenia Clinical sign or symptom manifested as debility, or lack or loss of strength and energy. | 0 | 2.05 | 1 | 0 |
Fascioliasis Liver disease caused by infections with parasitic flukes of the genus FASCIOLA, such as FASCIOLA HEPATICA. | 0 | 2.05 | 1 | 0 |
SAPHO Syndrome [description not available] | 0 | 2.07 | 1 | 0 |
Acquired Hyperostosis Syndrome Syndrome consisting of SYNOVITIS; ACNE CONGLOBATA; PALMOPLANTAR PUSTULOSIS; HYPEROSTOSIS; and OSTEITIS. The most common site of the disease is the upper anterior chest wall, characterized by predominantly osteosclerotic lesions, hyperostosis, and arthritis of the adjacent joints. The association of sterile inflammatory bone lesions and neutrophilic skin eruptions is indicative of this syndrome. | 0 | 2.07 | 1 | 0 |
Infections, RNA Virus [description not available] | 0 | 2.05 | 1 | 0 |
DNA Virus Infections Diseases caused by DNA VIRUSES. | 0 | 2.05 | 1 | 0 |
Arachnoid Membrane Inflammation [description not available] | 0 | 2.92 | 4 | 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 | 2.42 | 2 | 0 |
Hypotension, Postural [description not available] | 0 | 2.44 | 2 | 0 |
Cerebrospinal Fluid Effusion, Subdural [description not available] | 0 | 4.43 | 8 | 0 |
Hypotension, Orthostatic A significant drop in BLOOD PRESSURE after assuming a standing position. Orthostatic hypotension is a finding, and defined as a 20-mm Hg decrease in systolic pressure or a 10-mm Hg decrease in diastolic pressure 3 minutes after the person has risen from supine to standing. Symptoms generally include DIZZINESS, blurred vision, and SYNCOPE. | 0 | 2.44 | 2 | 0 |
Flaccid Quadriplegia [description not available] | 0 | 2.72 | 3 | 0 |
(pPNET) Peripheral Primitive Neuroectodermal Tumors [description not available] | 0 | 2.41 | 2 | 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 | 2.41 | 2 | 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 | 3.09 | 5 | 0 |
Benign Optic Nerve Neoplasm [description not available] | 0 | 3.12 | 5 | 0 |
Acute Necrotizing Encephalitis, Herpetic [description not available] | 0 | 2.05 | 1 | 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 | 2.05 | 1 | 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 | 3.6 | 9 | 0 |
Neuroma A tumor made up of nerve cells and nerve fibers. (Dorland, 27th ed) | 0 | 3.37 | 7 | 0 |
Cancer of the Ureter [description not available] | 0 | 4.04 | 5 | 0 |
Ureteral Neoplasms Cancer or tumors of the URETER which may cause obstruction leading to hydroureter, HYDRONEPHROSIS, and PYELONEPHRITIS. HEMATURIA is a common symptom. | 0 | 4.04 | 5 | 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 | 4.1 | 3 | 1 |
Embolic Infarction, Posterior Cerebral Artery [description not available] | 0 | 3.44 | 1 | 1 |
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 | 2.05 | 1 | 0 |
Cardiac Tamponade Compression of the heart by accumulated fluid (PERICARDIAL EFFUSION) or blood (HEMOPERICARDIUM) in the PERICARDIUM surrounding the heart. The affected cardiac functions and CARDIAC OUTPUT can range from minimal to total hemodynamic collapse. | 0 | 2.98 | 4 | 0 |
Experimental Radiation Injuries [description not available] | 0 | 3.25 | 6 | 0 |
Retroperitoneal Neoplasms New abnormal growth of tissue in the RETROPERITONEAL SPACE. | 0 | 2.92 | 4 | 0 |
Cranial Sinus Thrombosis [description not available] | 0 | 3.51 | 8 | 0 |
Fever of Unknown Origin Fever in which the etiology cannot be ascertained. | 0 | 2.46 | 2 | 0 |
Lipodystrophy, Intestinal [description not available] | 0 | 2.41 | 2 | 0 |
Disease, Pulmonary [description not available] | 0 | 4.86 | 13 | 0 |
Cancer of Mediastinum [description not available] | 0 | 4.01 | 5 | 0 |
Neoplasms, Pleural [description not available] | 0 | 2.42 | 2 | 0 |
Lung Diseases Pathological processes involving any part of the LUNG. | 0 | 9.86 | 13 | 0 |
Mediastinal Neoplasms Tumors or cancer of the MEDIASTINUM. | 0 | 4.01 | 5 | 0 |
Thoracic Neoplasms New abnormal growth of tissue in the THORAX. | 0 | 3.82 | 4 | 0 |
Psoriasis Arthropathica [description not available] | 0 | 2.69 | 3 | 0 |
Arthritis, Psoriatic A type of inflammatory arthritis associated with PSORIASIS, often involving the axial joints and the peripheral terminal interphalangeal joints. It is characterized by the presence of HLA-B27-associated SPONDYLARTHROPATHY, and the absence of rheumatoid factor. | 0 | 2.69 | 3 | 0 |
Hypercoagulability [description not available] | 0 | 2.05 | 1 | 0 |
Infections, Helicobacter [description not available] | 0 | 2.05 | 1 | 0 |
Gastritis Inflammation of the GASTRIC MUCOSA, a lesion observed in a number of unrelated disorders. | 0 | 2.05 | 1 | 0 |
Helicobacter Infections Infections with organisms of the genus HELICOBACTER, particularly, in humans, HELICOBACTER PYLORI. The clinical manifestations are focused in the stomach, usually the gastric mucosa and antrum, and the upper duodenum. This infection plays a major role in the pathogenesis of type B gastritis and peptic ulcer disease. | 0 | 2.05 | 1 | 0 |
Thrombophilia A disorder of HEMOSTASIS in which there is a tendency for the occurrence of THROMBOSIS. | 0 | 2.05 | 1 | 0 |
Impotence, Arteriogenic [description not available] | 0 | 2.05 | 1 | 0 |
Priapism A prolonged painful erection that may lasts hours and is not associated with sexual activity. It is seen in patients with SICKLE CELL ANEMIA, advanced malignancy, spinal trauma; and certain drug treatments. | 0 | 2.05 | 1 | 0 |
Antopol Disease [description not available] | 0 | 2.46 | 2 | 0 |
Polyneuropathy, Acquired [description not available] | 0 | 2.43 | 2 | 0 |
Polyneuropathies Diseases of multiple peripheral nerves simultaneously. Polyneuropathies usually are characterized by symmetrical, bilateral distal motor and sensory impairment with a graded increase in severity distally. The pathological processes affecting peripheral nerves include degeneration of the axon, myelin or both. The various forms of polyneuropathy are categorized by the type of nerve affected (e.g., sensory, motor, or autonomic), by the distribution of nerve injury (e.g., distal vs. proximal), by nerve component primarily affected (e.g., demyelinating vs. axonal), by etiology, or by pattern of inheritance. | 0 | 2.43 | 2 | 0 |
Leukemia, Acute Monocytic [description not available] | 0 | 2.05 | 1 | 0 |
Leukemia, Monocytic, Acute An acute myeloid leukemia in which 80% or more of the leukemic cells are of monocytic lineage including monoblasts, promonocytes, and MONOCYTES. | 0 | 2.05 | 1 | 0 |
Fibrous Dysplasia, Monostotic FIBROUS DYSPLASIA OF BONE involving only one bone. | 0 | 2.41 | 2 | 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 | 2.69 | 3 | 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 | 2.92 | 4 | 0 |
Female Genital Diseases [description not available] | 0 | 3.33 | 2 | 0 |
Genital Diseases, Female Pathological processes involving the female reproductive tract (GENITALIA, FEMALE). | 0 | 3.33 | 2 | 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 | 2.05 | 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 | 4.42 | 8 | 0 |
Glycogenosis [description not available] | 0 | 2.05 | 1 | 0 |
Glycogen Storage Disease A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement. | 0 | 2.05 | 1 | 0 |
Acute Autoimmune Neuropathy [description not available] | 0 | 2.44 | 2 | 0 |
Guillain-Barre Syndrome An acute inflammatory autoimmune neuritis caused by T cell- mediated cellular immune response directed towards peripheral myelin. Demyelination occurs in peripheral nerves and nerve roots. The process is often preceded by a viral or bacterial infection, surgery, immunization, lymphoma, or exposure to toxins. Common clinical manifestations include progressive weakness, loss of sensation, and loss of deep tendon reflexes. Weakness of respiratory muscles and autonomic dysfunction may occur. (From Adams et al., Principles of Neurology, 6th ed, pp1312-1314) | 0 | 7.44 | 2 | 0 |
Cancer of Maxillary Sinus [description not available] | 0 | 2.92 | 4 | 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 | 2.05 | 1 | 0 |
Angiofibroma A benign neoplasm of fibrous tissue in which there are numerous small and large, frequently dilated, vascular channels. (Stedman, 25th ed) | 0 | 2.05 | 1 | 0 |
Alport Syndrome [description not available] | 0 | 2.05 | 1 | 0 |
Nephritis, Hereditary A group of inherited conditions characterized initially by HEMATURIA and slowly progressing to RENAL INSUFFICIENCY. The most common form is the Alport syndrome (hereditary nephritis with HEARING LOSS) which is caused by mutations in genes for TYPE IV COLLAGEN and defective GLOMERULAR BASEMENT MEMBRANE. | 0 | 2.05 | 1 | 0 |
Familial Hypokalemic Periodic Paralysis [description not available] | 0 | 2.05 | 1 | 0 |
Hypokalemic Periodic Paralysis An autosomal dominant familial disorder characterized by recurrent episodes of skeletal muscle weakness associated with falls in serum potassium levels. The condition usually presents in the first or second decade of life with attacks of trunk and leg paresis during sleep or shortly after awakening. Symptoms may persist for hours to days and generally are precipitated by exercise or a meal high in carbohydrates. (Adams et al., Principles of Neurology, 6th ed, p1483) | 0 | 2.05 | 1 | 0 |
Lymphatic Abnormalities Congenital or acquired structural abnormalities of the lymphatic system (LYMPHOID TISSUE) including the lymph vessels. | 0 | 2.05 | 1 | 0 |
Angio-Osteohypertrophy Syndrome [description not available] | 0 | 2.46 | 2 | 0 |
C-C Fistula [description not available] | 0 | 2.45 | 2 | 0 |
Fibrocartilaginous Dysplasia of Bone [description not available] | 0 | 3.38 | 7 | 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 | 3.38 | 7 | 0 |
Hypertension, Renal Persistent high BLOOD PRESSURE due to KIDNEY DISEASES, such as those involving the renal parenchyma, the renal vasculature, or tumors that secrete RENIN. | 0 | 2.05 | 1 | 0 |
Labyrinthitis Inflammation of the inner ear (LABYRINTH). | 0 | 4.64 | 6 | 1 |
Axonal Injury, Diffuse [description not available] | 0 | 2.05 | 1 | 0 |
Adenocystic Carcinoma [description not available] | 0 | 3.37 | 7 | 0 |
Carcinoma, Adenoid Cystic Carcinoma characterized by bands or cylinders of hyalinized or mucinous stroma separating or surrounded by nests or cords of small epithelial cells. When the cylinders occur within masses of epithelial cells, they give the tissue a perforated, sievelike, or cribriform appearance. Such tumors occur in the mammary glands, the mucous glands of the upper and lower respiratory tract, and the salivary glands. They are malignant but slow-growing, and tend to spread locally via the nerves. (Dorland, 27th ed) | 0 | 3.37 | 7 | 0 |
Fibromuscular Dysplasia An idiopathic, segmental, nonatheromatous disease of the musculature of arterial walls, leading to STENOSIS of small and medium-sized arteries. There is true proliferation of SMOOTH MUSCLE CELLS and fibrous tissue. Fibromuscular dysplasia lesions are smooth stenosis and occur most often in the renal and carotid arteries. They may also occur in other peripheral arteries of the extremity. | 0 | 4.31 | 4 | 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 | 2.7 | 3 | 0 |
Mixed Pineocytoma-Pineoblastoma [description not available] | 0 | 2.06 | 1 | 0 |
Pinealoma Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670) | 0 | 2.06 | 1 | 0 |
Flank Pain Pain emanating from below the RIBS and above the ILIUM. | 0 | 2.97 | 1 | 0 |
Acute Renal Colic [description not available] | 0 | 2.97 | 1 | 0 |
Ureteral Calculi Stones in the URETER that are formed in the KIDNEY. They are rarely more than 5 mm in diameter for larger renal stones cannot enter ureters. They are often lodged at the ureteral narrowing and can cause excruciating renal colic. | 0 | 3.34 | 2 | 0 |
Bladder Calculi [description not available] | 0 | 2.97 | 1 | 0 |
Renal Colic A severe intermittent and spasmodic pain in the lower back radiating to the groin, scrotum, and labia which is most commonly caused by a kidney stone (RENAL CALCULUS) passing through the URETER or by other urinary track blockage. It is often associated with nausea, vomiting, fever, restlessness, dull pain, frequent urination, and HEMATURIA. | 0 | 2.97 | 1 | 0 |
Heritable Pulmonary Arterial Hypertension [description not available] | 0 | 2.05 | 1 | 0 |
Familial Primary Pulmonary Hypertension Familial or idiopathic hypertension in the PULMONARY CIRCULATION which is not secondary to other disease. | 0 | 2.05 | 1 | 0 |
Actinomycetoma [description not available] | 0 | 2.97 | 1 | 0 |
Mycetoma A chronic progressive subcutaneous infection caused by species of fungi (eumycetoma), or actinomycetes (actinomycetoma). It is characterized by tumefaction, abscesses, and tumor-like granules representing microcolonies of pathogens, such as MADURELLA fungi and bacteria ACTINOMYCETES, with different grain colors. | 0 | 2.97 | 1 | 0 |
Cancer of Paranasal Sinus [description not available] | 0 | 5.3 | 9 | 0 |
Paranasal Sinus Neoplasms Tumors or cancer of the PARANASAL SINUSES. | 0 | 5.3 | 9 | 0 |
Brachial Plexopathy [description not available] | 0 | 4.33 | 4 | 0 |
Brachial Plexus Neuropathies Diseases of the cervical (and first thoracic) roots, nerve trunks, cords, and peripheral nerve components of the BRACHIAL PLEXUS. Clinical manifestations include regional pain, PARESTHESIA; MUSCLE WEAKNESS, and decreased sensation (HYPESTHESIA) in the upper extremity. These disorders may be associated with trauma (including BIRTH INJURIES); THORACIC OUTLET SYNDROME; NEOPLASMS; NEURITIS; RADIOTHERAPY; and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp1351-2) | 0 | 4.33 | 4 | 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 | 2.05 | 1 | 0 |
Carcinoma, Lewis Lung A carcinoma discovered by Dr. Margaret R. Lewis of the Wistar Institute in 1951. This tumor originated spontaneously as a carcinoma of the lung of a C57BL mouse. The tumor does not appear to be grossly hemorrhagic and the majority of the tumor tissue is a semifirm homogeneous mass. (From Cancer Chemother Rep 2 1972 Nov;(3)1:325) It is also called 3LL and LLC and is used as a transplantable malignancy. | 0 | 2.46 | 2 | 0 |
Central Nervous System Lyme Disease [description not available] | 0 | 2.72 | 3 | 0 |
Aneurysm, Aortic [description not available] | 0 | 6.11 | 11 | 1 |
Prosthesis Durability [description not available] | 0 | 2.06 | 1 | 0 |
Aortic Aneurysm An abnormal balloon- or sac-like dilatation in the wall of AORTA. | 0 | 6.11 | 11 | 1 |
Alcoholic Cirrhosis [description not available] | 0 | 2.45 | 2 | 0 |
Liver Cirrhosis, Alcoholic FIBROSIS of the hepatic parenchyma due to chronic excess ALCOHOL DRINKING. | 0 | 2.45 | 2 | 0 |
Histoplasma capsulatum Infection [description not available] | 0 | 2.41 | 2 | 0 |
Cranial Nerve II Diseases [description not available] | 0 | 4.61 | 10 | 0 |
Histoplasmosis Infection resulting from exposure to the fungus HISTOPLASMA. It is worldwide in distribution and particularly common in the central and eastern states, especially areas around the Ohio and Mississippi River valleys. | 0 | 7.41 | 2 | 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 | 4.61 | 10 | 0 |
Pheochromocytoma, Extra-Adrenal [description not available] | 0 | 3.38 | 7 | 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 | 8.38 | 7 | 0 |
Graft Occlusion, Vascular Obstruction of flow in biological or prosthetic vascular grafts. | 0 | 3.27 | 6 | 0 |
Morbid Obesity [description not available] | 0 | 2.44 | 2 | 0 |
Obesity, Morbid The condition of weighing two, three, or more times the ideal weight, so called because it is associated with many serious and life-threatening disorders. In the BODY MASS INDEX, morbid obesity is defined as having a BMI greater than 40.0 kg/m2. | 0 | 2.44 | 2 | 0 |
Hematoma, Subdural Accumulation of blood in the SUBDURAL SPACE between the DURA MATER and the arachnoidal layer of the MENINGES. This condition primarily occurs over the surface of a CEREBRAL HEMISPHERE, but may develop in the spinal canal (HEMATOMA, SUBDURAL, SPINAL). Subdural hematoma can be classified as the acute or the chronic form, with immediate or delayed symptom onset, respectively. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 3.4 | 7 | 0 |
Bile Duct Obstruction [description not available] | 0 | 4.85 | 13 | 0 |
Hepatitis, Animal INFLAMMATION of the LIVER in non-human animals. | 0 | 2.71 | 3 | 0 |
Cholestasis Impairment of bile flow due to obstruction in small bile ducts (INTRAHEPATIC CHOLESTASIS) or obstruction in large bile ducts (EXTRAHEPATIC CHOLESTASIS). | 0 | 9.85 | 13 | 0 |
Bed Sores [description not available] | 0 | 2.06 | 1 | 0 |
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 | 2.06 | 1 | 0 |
Adjuvant Arthritis [description not available] | 0 | 2.73 | 3 | 0 |
Post-Dural Puncture Headache A secondary headache disorder attributed to low CEREBROSPINAL FLUID pressure caused by SPINAL PUNCTURE, usually after dural or lumbar puncture. | 0 | 2.06 | 1 | 0 |
Knee Dislocation Slippage of the FEMUR off the TIBIA. | 0 | 2.05 | 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 | 2.91 | 4 | 0 |
Pulmonary Consumption [description not available] | 0 | 2.72 | 3 | 0 |
Tuberculosis, Pulmonary MYCOBACTERIUM infections of the lung. | 0 | 2.72 | 3 | 0 |
Agrammatic Broca Aphasia [description not available] | 0 | 2.06 | 1 | 0 |
Anuria Absence of urine formation. It is usually associated with complete bilateral ureteral (URETER) obstruction, complete lower urinary tract obstruction, or unilateral ureteral obstruction when a solitary kidney is present. | 0 | 3.35 | 2 | 0 |
Delayed Postpartum Hemorrhage [description not available] | 0 | 2.98 | 1 | 0 |
Glomerular Necrosis [description not available] | 0 | 3.62 | 3 | 0 |
Postpartum Hemorrhage Excess blood loss from uterine bleeding associated with OBSTETRIC LABOR or CHILDBIRTH. It is defined as blood loss greater than 500 ml or of the amount that adversely affects the maternal physiology, such as BLOOD PRESSURE and HEMATOCRIT. Postpartum hemorrhage is divided into two categories, immediate (within first 24 hours after birth) or delayed (after 24 hours postpartum). | 0 | 2.98 | 1 | 0 |
Conjunctival Diseases Diseases involving the CONJUNCTIVA. | 0 | 2.41 | 2 | 0 |
Sclera Diseases [description not available] | 0 | 2.06 | 1 | 0 |
Cerebro-Hepato-Renal Syndrome [description not available] | 0 | 2.06 | 1 | 0 |
Zellweger Syndrome An autosomal recessive disorder due to defects in PEROXISOME biogenesis which involves more than 13 genes encoding peroxin proteins of the peroxisomal membrane and matrix. Zellweger syndrome is typically seen in the neonatal period with features such as dysmorphic skull; MUSCLE HYPOTONIA; SENSORINEURAL HEARING LOSS; visual compromise; SEIZURES; progressive degeneration of the KIDNEYS and the LIVER. Zellweger-like syndrome refers to phenotypes resembling the neonatal Zellweger syndrome but seen in children or adults with apparently intact peroxisome biogenesis. | 0 | 2.06 | 1 | 0 |
Coarctation of Aorta [description not available] | 0 | 3.71 | 10 | 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 | 3.71 | 10 | 0 |
Air Embolism [description not available] | 0 | 2.93 | 4 | 0 |
Hepatitis B Virus Infection [description not available] | 0 | 2.06 | 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 | 2.06 | 1 | 0 |
Chemodectoma [description not available] | 0 | 3.24 | 6 | 0 |
Glomus Tympanicum Tumor A rare PARAGANGLIOMA involving the GLOMUS TYMPANICUM, a collection of chemoreceptor tissue adjacent to the TYMPANIC CAVITY. It can cause TINNITUS and conductive hearing loss (HEARING LOSS, CONDUCTIVE). | 0 | 2.06 | 1 | 0 |
Hyperphosphatemia A condition of abnormally high level of PHOSPHATES in the blood, usually significantly above the normal range of 0.84-1.58 mmol per liter of serum. | 0 | 2.07 | 1 | 0 |
Fibrosis, Inflammatory Perianeurysmal [description not available] | 0 | 2.44 | 2 | 0 |
Retroperitoneal Fibrosis A slowly progressive condition of unknown etiology, characterized by deposition of fibrous tissue in the retroperitoneal space compressing the ureters, great vessels, bile duct, and other structures. When associated with abdominal aortic aneurysm, it may be called chronic periaortitis or inflammatory perianeurysmal fibrosis. | 0 | 7.44 | 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 | 2.98 | 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 | 3.36 | 2 | 0 |
Lymphoma of Mucosa-Associated Lymphoid Tissue [description not available] | 0 | 2.44 | 2 | 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 | 2.44 | 2 | 0 |
Esophageal Reflux [description not available] | 0 | 2.07 | 1 | 0 |
Esophageal Dysmotility [description not available] | 0 | 2.07 | 1 | 0 |
Gastroesophageal Reflux Retrograde flow of gastric juice (GASTRIC ACID) and/or duodenal contents (BILE ACIDS; PANCREATIC JUICE) into the distal ESOPHAGUS, commonly due to incompetence of the LOWER ESOPHAGEAL SPHINCTER. | 0 | 2.07 | 1 | 0 |
Adipocere [description not available] | 0 | 2.48 | 2 | 0 |
Bronze Diabetes [description not available] | 0 | 4.12 | 3 | 0 |
Enlarged Spleen [description not available] | 0 | 2.43 | 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 | 4.12 | 3 | 0 |
Acoustic Neurinoma, Bilateral [description not available] | 0 | 5.09 | 6 | 0 |
Deafness Unilateral [description not available] | 0 | 2.74 | 3 | 0 |
Neurofibromatosis 2 An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life. | 0 | 5.09 | 6 | 0 |
Albuminuria The presence of albumin in the urine, an indicator of KIDNEY DISEASES. | 0 | 2.98 | 1 | 0 |
Cancer, Second Primary [description not available] | 0 | 3.62 | 3 | 0 |
Multiple Endocrine Neoplasia Type 1 A form of multiple endocrine neoplasia that is characterized by the combined occurrence of tumors in the PARATHYROID GLANDS, the PITUITARY GLAND, and the PANCREATIC ISLETS. The resulting clinical signs include HYPERPARATHYROIDISM; HYPERCALCEMIA; HYPERPROLACTINEMIA; CUSHING DISEASE; GASTRINOMA; and ZOLLINGER-ELLISON SYNDROME. This disease is due to loss-of-function of the MEN1 gene, a tumor suppressor gene (GENES, TUMOR SUPPRESSOR) on CHROMOSOME 11 (Locus: 11q13). | 0 | 3.46 | 1 | 1 |
Weight Gain Increase in BODY WEIGHT over existing weight. | 0 | 2.07 | 1 | 0 |
Granulomatosis, Lipid [description not available] | 0 | 2.07 | 1 | 0 |
Erdheim-Chester Disease A rare form of non-Langerhans-cell histiocytosis (HISTIOCYTOSIS, NON-LANGERHANS-CELL) with onset in middle age. The systemic disease is characterized by infiltration of lipid-laden macrophages, multinucleated giant cells, an inflammatory infiltrate of lymphocytes and histiocytes in the bone marrow, and a generalized sclerosis of the long bones. | 0 | 2.07 | 1 | 0 |
Luft Disease [description not available] | 0 | 2.07 | 1 | 0 |
Chronic Progressive External Ophthalmoplegia with Myopathy [description not available] | 0 | 2.07 | 1 | 0 |
Encephalomyopathies, Mitochondrial [description not available] | 0 | 2.07 | 1 | 0 |
Mitochondrial Myopathies A group of muscle diseases associated with abnormal mitochondria function. | 0 | 2.07 | 1 | 0 |
Peliosis Hepatis A vascular disease of the LIVER characterized by the occurrence of multiple blood-filled CYSTS or cavities. The cysts are lined with ENDOTHELIAL CELLS; the cavities lined with hepatic parenchymal cells (HEPATOCYTES). Peliosis hepatis has been associated with use of anabolic steroids (ANABOLIC AGENTS) and certain drugs. | 0 | 2.08 | 1 | 0 |
Primary Hyperparathyroidism [description not available] | 0 | 2.07 | 1 | 0 |
Cancer of Parathyroid [description not available] | 0 | 2.91 | 4 | 0 |
Parathyroid Neoplasms Tumors or cancer of the PARATHYROID GLANDS. | 0 | 2.91 | 4 | 0 |
Hyperparathyroidism, Primary A condition of abnormally elevated output of PARATHYROID HORMONE due to parathyroid HYPERPLASIA or PARATHYROID NEOPLASMS. It is characterized by the combination of HYPERCALCEMIA, phosphaturia, elevated renal 1,25-DIHYDROXYVITAMIN D3 synthesis, and increased BONE RESORPTION. | 0 | 2.07 | 1 | 0 |
Carcinoma, Basal Cell, Pigmented [description not available] | 0 | 2.07 | 1 | 0 |
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 | 2.07 | 1 | 0 |
Epulides, Giant Cell [description not available] | 0 | 2.42 | 2 | 0 |
Aneurysmal Bone Cysts [description not available] | 0 | 3.34 | 2 | 0 |
Ameloblastoma An immature epithelial tumor of the JAW originating from the epithelial rests of Malassez or from other epithelial remnants of the ENAMEL from the developmental period. It is a slowly growing tumor, usually benign, but displays a marked propensity for invasive growth. | 0 | 2.07 | 1 | 0 |
Granuloma, Giant Cell A non-neoplastic inflammatory lesion, usually of the jaw or gingiva, containing large, multinucleated cells. It includes reparative giant cell granuloma. Peripheral giant cell granuloma refers to the gingiva (giant cell epulis); central refers to the jaw. | 0 | 2.42 | 2 | 0 |
Glomerulonephritis, Lupus [description not available] | 0 | 2.43 | 2 | 0 |
Lupus Nephritis Glomerulonephritis associated with autoimmune disease SYSTEMIC LUPUS ERYTHEMATOSUS. Lupus nephritis is histologically classified into 6 classes: class I - normal glomeruli, class II - pure mesangial alterations, class III - focal segmental glomerulonephritis, class IV - diffuse glomerulonephritis, class V - diffuse membranous glomerulonephritis, and class VI - advanced sclerosing glomerulonephritis (The World Health Organization classification 1982). | 0 | 2.43 | 2 | 0 |
Appendiceal Cancer [description not available] | 0 | 3.38 | 2 | 0 |
Appendiceal Neoplasms Tumors or cancer of the APPENDIX. | 0 | 3.38 | 2 | 0 |
Central Nervous System Schistosomiasis [description not available] | 0 | 2.07 | 1 | 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 | 2.99 | 1 | 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 | 2.99 | 1 | 0 |
Hereditary Optic Neuroretinopathy [description not available] | 0 | 2.07 | 1 | 0 |
Optic Atrophy, Hereditary, Leber A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001)) | 0 | 2.07 | 1 | 0 |
Adenocarcinoma, Endometrioid [description not available] | 0 | 2.44 | 2 | 0 |
Carcinoma, Endometrioid An adenocarcinoma characterized by the presence of cells resembling the glandular cells of the ENDOMETRIUM. It is a common histological type of ovarian CARCINOMA and ENDOMETRIAL CARCINOMA. There is a high frequency of co-occurrence of this form of adenocarcinoma in both tissues. | 0 | 2.44 | 2 | 0 |
Diseases of Nasopharynx [description not available] | 0 | 2.07 | 1 | 0 |
Cacosmia [description not available] | 0 | 2.07 | 1 | 0 |
Cardiac Free Wall Rupture [description not available] | 0 | 2.07 | 1 | 0 |
Kawasaki Disease [description not available] | 0 | 2.72 | 3 | 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 | 2.72 | 3 | 0 |
Aplasia Pure Red Cell [description not available] | 0 | 2.99 | 1 | 0 |
Fatty Liver with Encephalopathy [description not available] | 0 | 2.99 | 1 | 0 |
Red-Cell Aplasia, Pure Suppression of erythropoiesis with little or no abnormality of leukocyte or platelet production. | 0 | 2.99 | 1 | 0 |
Chronic Insomnia [description not available] | 0 | 2.07 | 1 | 0 |
Sleep Initiation and Maintenance Disorders Disorders characterized by impairment of the ability to initiate or maintain sleep. This may occur as a primary disorder or in association with another medical or psychiatric condition. | 0 | 2.07 | 1 | 0 |
Cold Panniculitis [description not available] | 0 | 2.07 | 1 | 0 |
Lipodystrophy A collection of heterogenous conditions resulting from defective LIPID METABOLISM and characterized by ADIPOSE TISSUE atrophy. Often there is redistribution of body fat resulting in peripheral fat wasting and central adiposity. They include generalized, localized, congenital, and acquired lipodystrophy. | 0 | 2.41 | 2 | 0 |
Bartonella henselae Infection [description not available] | 0 | 2.07 | 1 | 0 |
Cat-Scratch Disease A self-limiting bacterial infection of the regional lymph nodes caused by AFIPIA felis, a gram-negative bacterium recently identified by the Centers for Disease Control and Prevention and by BARTONELLA HENSELAE. It usually arises one or more weeks following a feline scratch, with raised inflammatory nodules at the site of the scratch being the primary symptom. | 0 | 2.07 | 1 | 0 |
Altitude Hypoxia Low ambient oxygen tension associated with ALTITUDE. | 0 | 2.05 | 1 | 0 |
Altitude Sickness Multiple symptoms associated with reduced oxygen at high ALTITUDE. | 0 | 2.05 | 1 | 0 |
Angiolipoma A benign neoplasm composed of a mixture of adipose tissue and blood vessels. (Dorland, 27th ed) | 0 | 2.48 | 2 | 0 |
Benign Hypothalamic Neoplasms [description not available] | 0 | 2.7 | 3 | 0 |
Cerebral Primitive Neuroectodermal Tumor [description not available] | 0 | 2.08 | 1 | 0 |
Neuroectodermal Tumors, Primitive A group of malignant tumors of the nervous system that feature primitive cells with elements of neuronal and/or glial differentiation. Use of this term is limited by some authors to central nervous system tumors and others include neoplasms of similar origin which arise extracranially (i.e., NEUROECTODERMAL TUMORS, PRIMITIVE, PERIPHERAL). This term is also occasionally used as a synonym for MEDULLOBLASTOMA. In general, these tumors arise in the first decade of life and tend to be highly malignant. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2059) | 0 | 2.08 | 1 | 0 |
Destombes-Rosai-Dorfman Syndrome [description not available] | 0 | 2.08 | 1 | 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 | 2.08 | 1 | 0 |
Cerebral Cryptococcosis [description not available] | 0 | 2.72 | 3 | 0 |
Meningitis, Cryptococcal Meningeal inflammation produced by CRYPTOCOCCUS NEOFORMANS, an encapsulated yeast that tends to infect individuals with ACQUIRED IMMUNODEFICIENCY SYNDROME and other immunocompromised states. The organism enters the body through the respiratory tract, but symptomatic infections are usually limited to the lungs and nervous system. The organism may also produce parenchymal brain lesions (torulomas). Clinically, the course is subacute and may feature HEADACHE; NAUSEA; PHOTOPHOBIA; focal neurologic deficits; SEIZURES; cranial neuropathies; and HYDROCEPHALUS. (From Adams et al., Principles of Neurology, 6th ed, pp721-2) | 0 | 2.72 | 3 | 0 |
Complication, Intraoperative [description not available] | 0 | 2.93 | 4 | 0 |
Swine Diseases Diseases of domestic swine and of the wild boar of the genus Sus. | 0 | 2.07 | 1 | 0 |
Cranial Nerve V Injury [description not available] | 0 | 2.08 | 1 | 0 |
Cranial Nerve XII Injury [description not available] | 0 | 2.43 | 2 | 0 |
Dermoid [description not available] | 0 | 2.44 | 2 | 0 |
Cystic Echinococcosis [description not available] | 0 | 3.26 | 6 | 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 | 2.42 | 2 | 0 |
Microsatellite Instability The occurrence of highly polymorphic mono- and dinucleotide MICROSATELLITE REPEATS in somatic cells. It is a form of genome instability associated with defects in DNA MISMATCH REPAIR. | 0 | 2.08 | 1 | 0 |
Adenoma, Hepatocellular [description not available] | 0 | 2.42 | 2 | 0 |
Chondrosteoma [description not available] | 0 | 2.71 | 3 | 0 |
Femoral Neoplasms New abnormal growth of tissue in the FEMUR. | 0 | 3.25 | 6 | 0 |
Vascular Injuries [description not available] | 0 | 2.08 | 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 | 3.62 | 3 | 0 |
Criss-cross Heart [description not available] | 0 | 2.41 | 2 | 0 |
Spondylisthesis [description not available] | 0 | 3.33 | 2 | 0 |
Infantile Respiratory Distress Syndrome [description not available] | 0 | 2.01 | 1 | 0 |
Respiratory Distress Syndrome, Newborn A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause. | 0 | 2.01 | 1 | 0 |
Bladder Diseases [description not available] | 0 | 5.21 | 4 | 1 |
Wounds, Gunshot Disruption of structural continuity of the body as a result of the discharge of firearms. | 0 | 3.79 | 2 | 1 |
Deficiency, Thiamine [description not available] | 0 | 2.69 | 3 | 0 |
Thiamine Deficiency A nutritional condition produced by a deficiency of THIAMINE in the diet, characterized by anorexia, irritability, and weight loss. Later, patients experience weakness, peripheral neuropathy, headache, and tachycardia. In addition to being caused by a poor diet, thiamine deficiency in the United States most commonly occurs as a result of alcoholism, since ethanol interferes with thiamine absorption. In countries relying on polished rice as a dietary staple, BERIBERI prevalence is very high. (From Cecil Textbook of Medicine, 19th ed, p1171) | 0 | 2.69 | 3 | 0 |
Abscess, Retropharyngeal [description not available] | 0 | 2.92 | 1 | 0 |
Osteophytosis, Spinal [description not available] | 0 | 3.31 | 2 | 0 |
Abscess, Psoas [description not available] | 0 | 2.92 | 1 | 0 |
Cirrhoses, Experimental Liver [description not available] | 0 | 3.1 | 5 | 0 |
Sexually Transmitted Diseases Diseases due to or propagated by sexual contact. | 0 | 2.01 | 1 | 0 |
Anorexia Nervosa An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994) | 0 | 2.01 | 1 | 0 |
Injuries, Spinal [description not available] | 0 | 7.32 | 6 | 0 |
Acidosis, Renal Tubular, Type I [description not available] | 0 | 2.01 | 1 | 0 |
Acidosis, Renal Tubular A group of genetic disorders of the KIDNEY TUBULES characterized by the accumulation of metabolically produced acids with elevated plasma chloride, hyperchloremic metabolic ACIDOSIS. Defective renal acidification of URINE (proximal tubules) or low renal acid excretion (distal tubules) can lead to complications such as HYPOKALEMIA, hypercalcinuria with NEPHROLITHIASIS and NEPHROCALCINOSIS, and RICKETS. | 0 | 2.01 | 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 | 2.42 | 2 | 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 | 2.42 | 2 | 0 |
Nevoxanthoendothelioma [description not available] | 0 | 2.01 | 1 | 0 |
Pain, Intractable Persistent pain that is refractory to some or all forms of treatment. | 0 | 2.01 | 1 | 0 |
Dysarthosis [description not available] | 0 | 2.01 | 1 | 0 |
Malignant Neurilemmoma [description not available] | 0 | 2.01 | 1 | 0 |
Amentia [description not available] | 0 | 2.01 | 1 | 0 |
Angiomatosis Retinae [description not available] | 0 | 3.09 | 5 | 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 | 2.01 | 1 | 0 |
von Hippel-Lindau Disease An autosomal dominant disorder caused by mutations in a tumor suppressor gene. This syndrome is characterized by abnormal growth of small blood vessels leading to a host of neoplasms. They include HEMANGIOBLASTOMA in the RETINA; CEREBELLUM; and SPINAL CORD; PHEOCHROMOCYTOMA; pancreatic tumors; and renal cell carcinoma (see CARCINOMA, RENAL CELL). Common clinical signs include HYPERTENSION and neurological dysfunctions. | 0 | 3.09 | 5 | 0 |
Basilar Artery Insufficiency [description not available] | 0 | 2.7 | 3 | 0 |
Lymphocytosis Excess of normal lymphocytes in the blood or in any effusion. | 0 | 2.01 | 1 | 0 |
Arteriosclerosis Thickening and loss of elasticity of the walls of ARTERIES of all sizes. There are many forms classified by the types of lesions and arteries involved, such as ATHEROSCLEROSIS with fatty lesions in the ARTERIAL INTIMA of medium and large muscular arteries. | 0 | 8.61 | 24 | 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 | 2.01 | 1 | 0 |
Ganglion Cysts Nodular tumor-like lesions or mucoid flesh, arising from tendon sheaths, LIGAMENTS, or JOINT CAPSULE, especially of the hands, wrists, or feet. They are not true cysts as they lack epithelial wall. They are distinguished from SYNOVIAL CYSTS by the lack of communication with a joint cavity or the SYNOVIAL MEMBRANE. | 0 | 2.71 | 3 | 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 | 9.66 | 6 | 0 |
Bacteroidaceae Infections Infections with bacteria of the family BACTEROIDACEAE. | 0 | 2.01 | 1 | 0 |
Actinomyces Infections [description not available] | 0 | 2.4 | 2 | 0 |
Convulsive Generalized Seizure Disorder [description not available] | 0 | 2.01 | 1 | 0 |
Bacterial Infections, Gram-Positive [description not available] | 0 | 2.69 | 3 | 0 |
Group A Strep Infection [description not available] | 0 | 4.7 | 11 | 0 |
Fusobacterium Infections Infections with bacteria of the genus FUSOBACTERIUM. | 0 | 2.69 | 3 | 0 |
Streptococcal Infections Infections with bacteria of the genus STREPTOCOCCUS. | 0 | 4.7 | 11 | 0 |
Gram-Positive Bacterial Infections Infections caused by bacteria that retain the crystal violet stain (positive) when treated by the gram-staining method. | 0 | 2.69 | 3 | 0 |
Central Nervous System Tuberculosis [description not available] | 0 | 2.01 | 1 | 0 |
Empyema Presence of pus in a hollow organ or body cavity. | 0 | 2.93 | 1 | 0 |
Carotid Body Tumor Benign paraganglioma at the bifurcation of the COMMON CAROTID ARTERIES. It can encroach on the parapharyngeal space and produce dysphagia, pain, and cranial nerve palsies. | 0 | 2.67 | 3 | 0 |
Hyperoxia An abnormal increase in the amount of oxygen in the tissues and organs. | 0 | 2.01 | 1 | 0 |
Proteinuria The presence of proteins in the urine, an indicator of KIDNEY DISEASES. | 0 | 3.81 | 2 | 1 |
Marfan Syndrome, Type I [description not available] | 0 | 2.01 | 1 | 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 | 2.01 | 1 | 0 |
Hepatitis, Infectious [description not available] | 0 | 1.93 | 1 | 0 |
Hepatitis A INFLAMMATION of the LIVER in humans caused by a member of the HEPATOVIRUS genus, HUMAN HEPATITIS A VIRUS. It can be transmitted through fecal contamination of food or water. | 0 | 1.93 | 1 | 0 |
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 | 3.32 | 2 | 0 |
Alcoholic Fatty Liver [description not available] | 0 | 2.68 | 3 | 0 |
Bronchiolitis, Exudative [description not available] | 0 | 2.01 | 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 | 2.01 | 1 | 0 |
Paraparesis Mild to moderate loss of bilateral lower extremity motor function, which may be a manifestation of SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; MUSCULAR DISEASES; INTRACRANIAL HYPERTENSION; parasagittal brain lesions; and other conditions. | 0 | 2.01 | 1 | 0 |
Granuloma, Hodgkin [description not available] | 0 | 3.09 | 5 | 0 |
Hodgkin Disease A malignant disease characterized by progressive enlargement of the lymph nodes, spleen, and general lymphoid tissue. In the classical variant, giant usually multinucleate Hodgkin's and REED-STERNBERG CELLS are present; in the nodular lymphocyte predominant variant, lymphocytic and histiocytic cells are seen. | 0 | 3.09 | 5 | 0 |
Taste Disorder, Anterior Tongue [description not available] | 0 | 2.01 | 1 | 0 |
Male Genitourinary Diseases [description not available] | 0 | 2.93 | 1 | 0 |
Female Genitourinary Diseases [description not available] | 0 | 2.93 | 1 | 0 |
Conjugate Nystagmus [description not available] | 0 | 2.02 | 1 | 0 |
Polyomavirus Infections Infections with POLYOMAVIRUS, which are often cultured from the urine of kidney transplant patients. Excretion of BK VIRUS is associated with ureteral strictures and CYSTITIS, and that of JC VIRUS with progressive multifocal leukoencephalopathy (LEUKOENCEPHALOPATHY, PROGRESSIVE MULTIFOCAL). | 0 | 2.02 | 1 | 0 |
Fibroma, Shope [description not available] | 0 | 3.33 | 2 | 0 |
Compartment Syndromes Conditions in which increased pressure within a limited space compromises the BLOOD CIRCULATION and function of tissue within that space. Some of the causes of increased pressure are TRAUMA, tight dressings, HEMORRHAGE, and exercise. Sequelae include nerve compression (NERVE COMPRESSION SYNDROMES); PARALYSIS; and ISCHEMIC CONTRACTURE. FASCIOTOMY is often used to decompress increased pressure and eliminate pain associated with compartment syndromes. | 0 | 2.01 | 1 | 0 |
Branch Retinal Artery Occlusion [description not available] | 0 | 2.93 | 1 | 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 | 2.93 | 1 | 0 |
Encephalitis, West Nile Fever [description not available] | 0 | 2.01 | 1 | 0 |
West Nile Fever A mosquito-borne viral illness caused by the WEST NILE VIRUS, a FLAVIVIRUS and endemic to regions of Africa, Asia, and Europe. Common clinical features include HEADACHE; FEVER; maculopapular rash; gastrointestinal symptoms; and lymphadenopathy. MENINGITIS; ENCEPHALITIS; and MYELITIS may also occur. The disease may occasionally be fatal or leave survivors with residual neurologic deficits. (From Joynt, Clinical Neurology, 1996, Ch26, p13; Lancet 1998 Sep 5;352(9130):767-71) | 0 | 2.01 | 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 | 3.32 | 2 | 0 |
Fifth Phacomatosis [description not available] | 0 | 2.02 | 1 | 0 |
Basal Cell Nevus Syndrome Hereditary disorder consisting of multiple basal cell carcinomas, odontogenic keratocysts, and multiple skeletal defects, e.g., frontal and temporoparietal bossing, bifurcated and splayed ribs, kyphoscoliosis, fusion of vertebrae, and cervicothoracic spina bifida. Genetic transmission is autosomal dominant. | 0 | 2.02 | 1 | 0 |
Acute-Phase Reaction An early local inflammatory reaction to insult or injury that consists of fever, an increase in inflammatory humoral factors, and an increased synthesis by hepatocytes of a number of proteins or glycoproteins usually found in the plasma. | 0 | 2.01 | 1 | 0 |
Neurocytoma A benign brain tumor composed of neural elements which most often arise from the SEPTUM PELLUCIDUM and the walls of the lateral ventricles. Immunohistochemistry and electron microscopy evaluations may reveal expression of neuron specific enolase and synaptophysin and cells containing microtubuli, neurosecretory granules, and presynaptic vesicles. (From Acta Med Port 1994 Feb;7(2):113-9) | 0 | 3.32 | 2 | 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 | 3.33 | 2 | 0 |
Mediastinal Diseases Disorders of the mediastinum, general or unspecified. | 0 | 2.41 | 2 | 0 |
Diseases of Pharynx [description not available] | 0 | 2.02 | 1 | 0 |
Adenosis of Breast [description not available] | 0 | 5.32 | 8 | 0 |
Fibrocystic Breast Disease A common and benign breast disease characterized by varying degree of fibrocystic changes in the breast tissue. There are three major patterns of morphological changes, including FIBROSIS, formation of CYSTS, and proliferation of glandular tissue (adenosis). The fibrocystic breast has a dense irregular, lumpy, bumpy consistency. | 0 | 5.32 | 8 | 0 |
Craniofacial Pain [description not available] | 0 | 2.41 | 2 | 0 |
Facial Pain Pain in the facial region including orofacial pain and craniofacial pain. Associated conditions include local inflammatory and neoplastic disorders and neuralgic syndromes involving the trigeminal, facial, and glossopharyngeal nerves. Conditions which feature recurrent or persistent facial pain as the primary manifestation of disease are referred to as FACIAL PAIN SYNDROMES. | 0 | 2.41 | 2 | 0 |
Baker Cyst [description not available] | 0 | 2.02 | 1 | 0 |
Craniocerebral Injuries [description not available] | 0 | 2.02 | 1 | 0 |
Acquired Meningocele [description not available] | 0 | 3.32 | 2 | 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 | 2.02 | 1 | 0 |
Herpes Zoster, Ocular [description not available] | 0 | 2.02 | 1 | 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 | 2.02 | 1 | 0 |
Angiomyxoma [description not available] | 0 | 3.11 | 5 | 0 |
Foreign-Body Granuloma [description not available] | 0 | 2.69 | 3 | 0 |
Gastrointestinal Stromal Neoplasm [description not available] | 0 | 2.02 | 1 | 0 |
Gastrointestinal Stromal Tumors All tumors in the GASTROINTESTINAL TRACT arising from mesenchymal cells (MESODERM) except those of smooth muscle cells (LEIOMYOMA) or Schwann cells (SCHWANNOMA). | 0 | 2.02 | 1 | 0 |
Atypical Mycobacterial Infection, Disseminated [description not available] | 0 | 2.02 | 1 | 0 |
Carcinoma, Papillary A malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. (Stedman, 25th ed) | 0 | 2.68 | 3 | 0 |
Cumulative Trauma Disorders Harmful and painful condition caused by overuse or overexertion of some part of the musculoskeletal system, often resulting from work-related physical activities. It is characterized by inflammation, pain, or dysfunction of the involved joints, bones, ligaments, and nerves. | 0 | 2.02 | 1 | 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 | 2.41 | 2 | 0 |
Cancer of Muscle [description not available] | 0 | 5.52 | 16 | 0 |
Granular Cell Myoblastoma [description not available] | 0 | 3.79 | 2 | 0 |
Retrocochlear Diseases Pathological processes involving the VESTIBULOCOCHLEAR NERVE; BRAINSTEM; or CENTRAL NERVOUS SYSTEM. When hearing loss is due to retrocochlear pathology, it is called retrocochlear hearing loss. | 0 | 3.4 | 1 | 1 |
Muscle Relaxation That phase of a muscle twitch during which a muscle returns to a resting position. | 0 | 2.43 | 2 | 0 |
Adult-Onset Dystonias [description not available] | 0 | 2.02 | 1 | 0 |
Dystonic Disorders Acquired and inherited conditions that feature DYSTONIA as a primary manifestation of disease. These disorders are generally divided into generalized dystonias (e.g., dystonia musculorum deformans) and focal dystonias (e.g., writer's cramp). They are also classified by patterns of inheritance and by age of onset. | 0 | 2.02 | 1 | 0 |
Aldosteronism [description not available] | 0 | 7.02 | 1 | 0 |
Hyperaldosteronism A condition caused by the overproduction of ALDOSTERONE. It is characterized by sodium retention and potassium excretion with resultant HYPERTENSION and HYPOKALEMIA. | 0 | 2.02 | 1 | 0 |
Tendinitis Inflammation of TENDONS. It is characterized by the degeneration of tendons accompanied by an inflammatory repair response, fibroblastic proliferation, and formation of granulation tissue. Tendinitis is not a clinical diagnosis and can be confirmed only by histopathological findings. | 0 | 2.69 | 3 | 0 |
Tendinopathy Clinical syndrome describing overuse tendon injuries characterized by a combination of PAIN, diffuse or localized swelling, and impaired performance. | 0 | 2.69 | 3 | 0 |
Coronary Artery Vasospasm [description not available] | 0 | 2.02 | 1 | 0 |
Coronary Vasospasm Spasm of the large- or medium-sized coronary arteries. | 0 | 2.02 | 1 | 0 |
Cataract, Membranous [description not available] | 0 | 2.02 | 1 | 0 |
Amyloid Neuropathies Disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. Familial, primary (nonfamilial), and secondary forms have been described. Some familial subtypes demonstrate an autosomal dominant pattern of inheritance. Clinical manifestations include sensory loss, mild weakness, autonomic dysfunction, and CARPAL TUNNEL SYNDROME. (Adams et al., Principles of Neurology, 6th ed, p1349) | 0 | 2.41 | 2 | 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) | 0 | 2.02 | 1 | 0 |
Vaginal Discharge A common gynecologic disorder characterized by an abnormal, nonbloody discharge from the genital tract. | 0 | 2.02 | 1 | 0 |
Benedict Syndrome [description not available] | 0 | 2.02 | 1 | 0 |
Acquired Metabolic Diseases, Brain [description not available] | 0 | 2.02 | 1 | 0 |
Amnesia, Pre-Ictal [description not available] | 0 | 2.02 | 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 | 2.4 | 2 | 0 |
Nephrosis Pathological processes of the KIDNEY without inflammatory or neoplastic components. Nephrosis may be a primary disorder or secondary complication of other diseases. It is characterized by the NEPHROTIC SYNDROME indicating the presence of PROTEINURIA and HYPOALBUMINEMIA with accompanying EDEMA. | 0 | 2.02 | 1 | 0 |
Ganglioneuroblastoma A moderately malignant neoplasm composed of primitive neuroectodermal cells dispersed in myxomatous or fibrous stroma intermixed with mature ganglion cells. It may undergo transformation into a neuroblastoma. It arises from the sympathetic trunk or less frequently from the adrenal medulla, cerebral cortex, and other locations. Cervical ganglioneuroblastomas may be associated with HORNER SYNDROME and the tumor may occasionally secrete vasoactive intestinal peptide, resulting in chronic diarrhea. | 0 | 2.02 | 1 | 0 |
Hemiplegia, Crossed [description not available] | 0 | 2.92 | 4 | 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 | 2.92 | 4 | 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 | 3.41 | 1 | 1 |
Abdominal Injuries General or unspecified injuries involving organs in the abdominal cavity. | 0 | 2.02 | 1 | 0 |
Elephantiasis Neuromatosis [description not available] | 0 | 2.02 | 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 | 2.02 | 1 | 0 |
Carcinoma, Lobular A type of BREAST CANCER where the abnormal malignant cells form in the lobules, or milk-producing glands, of the breast. | 0 | 2.69 | 3 | 0 |
Acquired Vocal Cord Palsy [description not available] | 0 | 2.02 | 1 | 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 | 2.02 | 1 | 0 |
Hypopharyngeal Cancer [description not available] | 0 | 3.08 | 5 | 0 |
Hypopharyngeal Neoplasms Tumors or cancer of the HYPOPHARYNX. | 0 | 3.08 | 5 | 0 |
Periostitis Inflammation of the periosteum. The condition is generally chronic, and is marked by tenderness and swelling of the bone and an aching pain. Acute periostitis is due to infection, is characterized by diffuse suppuration, severe pain, and constitutional symptoms, and usually results in necrosis. (Dorland, 27th ed) | 0 | 2.02 | 1 | 0 |
Infection, Toxoplasma gondii [description not available] | 0 | 2.41 | 2 | 0 |
Toxoplasmosis The acquired form of infection by Toxoplasma gondii in animals and man. | 0 | 2.41 | 2 | 0 |
Adenoma Sebaceum Facial ANGIOFIBROMA in tuberous sclerosis | 0 | 4.71 | 2 | 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 | 4.71 | 2 | 0 |
Oligomenorrhea Abnormally infrequent menstruation. | 0 | 2.02 | 1 | 0 |
Patency of the Ductus Arteriosus [description not available] | 0 | 2.02 | 1 | 0 |
Ductus Arteriosus, Patent A congenital heart defect characterized by the persistent opening of fetal DUCTUS ARTERIOSUS that connects the PULMONARY ARTERY to the descending aorta (AORTA, DESCENDING) allowing unoxygenated blood to bypass the lung and flow to the PLACENTA. Normally, the ductus is closed shortly after birth. | 0 | 2.02 | 1 | 0 |
Legionellosis Infections with bacteria of the genus LEGIONELLA. | 0 | 2.02 | 1 | 0 |
Depression, Involutional Form of depression in those MIDDLE AGE with feelings of ANXIETY. | 0 | 2.03 | 1 | 0 |
Inadequate Sleep [description not available] | 0 | 2.03 | 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 | 2.03 | 1 | 0 |
Infections, Pseudomonas [description not available] | 0 | 2.03 | 1 | 0 |
Pseudomonas Infections Infections with bacteria of the genus PSEUDOMONAS. | 0 | 2.03 | 1 | 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 | 3.31 | 2 | 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 | 2.92 | 4 | 0 |
Cardiac Output, Low A state of subnormal or depressed cardiac output at rest or during stress. It is a characteristic of CARDIOVASCULAR DISEASES, including congenital, valvular, rheumatic, hypertensive, coronary, and cardiomyopathic. The serious form of low cardiac output is characterized by marked reduction in STROKE VOLUME, and systemic vasoconstriction resulting in cold, pale, and sometimes cyanotic extremities. | 0 | 3.35 | 2 | 0 |
Central European Encephalitis [description not available] | 0 | 2.03 | 1 | 0 |
Convergent Strabismus [description not available] | 0 | 2.03 | 1 | 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 | 2.03 | 1 | 0 |
Cranial Nerve IX Diseases [description not available] | 0 | 2.03 | 1 | 0 |
Abnormal Deep Tendon Reflex [description not available] | 0 | 2.03 | 1 | 0 |
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 | 2.03 | 1 | 0 |
Glossopharyngeal Nerve Diseases Diseases of the ninth cranial (glossopharyngeal) nerve or its nuclei in the medulla. The nerve may be injured by diseases affecting the lower brain stem, floor of the posterior fossa, jugular foramen, or the nerve's extracranial course. Clinical manifestations include loss of sensation from the pharynx, decreased salivation, and syncope. Glossopharyngeal neuralgia refers to a condition that features recurrent unilateral sharp pain in the tongue, angle of the jaw, external auditory meatus and throat that may be associated with SYNCOPE. Episodes may be triggered by cough, sneeze, swallowing, or pressure on the tragus of the ear. (Adams et al., Principles of Neurology, 6th ed, p1390) | 0 | 2.03 | 1 | 0 |
Shaken Baby Syndrome Brain injuries resulted from vigorous shaking of an infant or young child held by the chest, shoulders, or extremities causing extreme cranial acceleration. It is characterized by the intracranial and intraocular hemorrhages with no evident external trauma. Serious cases may result in death. | 0 | 2.03 | 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 | 7.03 | 1 | 0 |
Submandibular Gland Neoplasms New abnormal growth of tissue in the SUBMANDIBULAR GLAND. | 0 | 2.03 | 1 | 0 |
Facial Asymmetry Congenital or acquired asymmetry of the face. | 0 | 2.03 | 1 | 0 |
Infections, Respiratory [description not available] | 0 | 9.64 | 9 | 9 |
Respiratory Tract Infections Invasion of the host RESPIRATORY SYSTEM by microorganisms, usually leading to pathological processes or diseases. | 0 | 9.64 | 9 | 9 |
Duodenal Diseases Pathological conditions in the DUODENUM region of the small intestine (INTESTINE, SMALL). | 0 | 2.7 | 3 | 0 |
Diverticulitis Inflammation of a DIVERTICULUM or diverticula. | 0 | 2.03 | 1 | 0 |
Decerebrate Posturing [description not available] | 0 | 2.42 | 2 | 0 |
Bacterial Endocarditides [description not available] | 0 | 2.92 | 4 | 0 |
Arterial Diseases, Cerebral [description not available] | 0 | 2.41 | 2 | 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 | 2.41 | 2 | 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 | 2.92 | 4 | 0 |
Pancytopenia Deficiency of all three cell elements of the blood, erythrocytes, leukocytes and platelets. | 0 | 2.03 | 1 | 0 |
Common Peroneal Nerve Entrapment [description not available] | 0 | 3.81 | 2 | 1 |
Chorea Disorders [description not available] | 0 | 2.41 | 2 | 0 |
Chorea Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES. | 0 | 2.41 | 2 | 0 |
Sprains [description not available] | 0 | 2.41 | 2 | 0 |
Ankle Injuries Harm or hurt to the ankle or ankle joint usually inflicted by an external source. | 0 | 2.69 | 3 | 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 | 2.41 | 2 | 0 |
Cancer of the Vulva [description not available] | 0 | 2.44 | 2 | 0 |
Vulvar Neoplasms Tumors or cancer of the VULVA. | 0 | 2.44 | 2 | 0 |
Complications, Hematologic Pregnancy [description not available] | 0 | 2.03 | 1 | 0 |
Theca Cell Tumor [description not available] | 0 | 2.03 | 1 | 0 |
Drug Overdose Accidental or deliberate use of a medication or street drug in excess of normal dosage. | 0 | 2.03 | 1 | 0 |
Cholecystoduodenal Fistula [description not available] | 0 | 2.03 | 1 | 0 |
AIDS Arteritis, Central Nervous System Inflammation of ARTERIES in the CENTRAL NERVOUS SYSTEM that occurs in patients with ACQUIRED IMMUNODEFICIENCY SYNDROME or AIDS-RELATED OPPORTUNISTIC INFECTIONS. | 0 | 2.03 | 1 | 0 |
Fungal Lung Diseases [description not available] | 0 | 2.03 | 1 | 0 |
Blastomycosis, North American [description not available] | 0 | 2.42 | 2 | 0 |
Agricultural Worker Disease [description not available] | 0 | 2.03 | 1 | 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 | 2.42 | 2 | 0 |
Skin Ulcer An ULCER of the skin and underlying tissues. | 0 | 2.03 | 1 | 0 |
Autosomal Hemophilia A [description not available] | 0 | 2.41 | 2 | 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 | 2.41 | 2 | 0 |
Central Nervous System Syphilis [description not available] | 0 | 2.41 | 2 | 0 |
Benign Monoclonal Gammopathies [description not available] | 0 | 2.03 | 1 | 0 |
Common Migraine [description not available] | 0 | 2.03 | 1 | 0 |
Migraine without Aura Recurrent unilateral pulsatile headaches, not preceded or accompanied by an aura, in attacks lasting 4-72 hours. It is characterized by PAIN of moderate to severe intensity; aggravated by physical activity; and associated with NAUSEA and / or PHOTOPHOBIA and PHONOPHOBIA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1) | 0 | 2.03 | 1 | 0 |
Albright Syndrome [description not available] | 0 | 3.6 | 3 | 0 |
Fibrous Dysplasia, Polyostotic FIBROUS DYSPLASIA OF BONE affecting several bones. When melanotic pigmentation (CAFE-AU-LAIT SPOTS) and multiple endocrine hyperfunction are additionally associated it is referred to as Albright syndrome. | 0 | 3.6 | 3 | 0 |
Cancer of Lip [description not available] | 0 | 2.03 | 1 | 0 |
Lip Diseases Diseases involving the LIP. | 0 | 2.03 | 1 | 0 |
Adenomatous Polyps Benign neoplasms derived from glandular epithelium. (From Stedman, 25th ed) | 0 | 2.03 | 1 | 0 |
Cholangioma [description not available] | 0 | 3.6 | 3 | 0 |
Adenoma, Bile Duct A benign tumor of the intrahepatic bile ducts. | 0 | 3.6 | 3 | 0 |
Alcohol Abuse, Nervous System [description not available] | 0 | 2.03 | 1 | 0 |
Lower Extremity Weakness, Spastic [description not available] | 0 | 2.03 | 1 | 0 |
Adenoma, beta-Cell [description not available] | 0 | 2.92 | 4 | 0 |
Insulinoma A benign tumor of the PANCREATIC BETA CELLS. Insulinoma secretes excess INSULIN resulting in HYPOGLYCEMIA. | 0 | 7.92 | 4 | 0 |
Chondroma A benign neoplasm derived from mesodermal cells that form cartilage. It may remain within the substance of a cartilage or bone (true chondroma or enchondroma) or may develop on the surface of a cartilage (ecchondroma or ecchondrosis). (Dorland, 27th ed; Stedman, 25th ed) | 0 | 2.42 | 2 | 0 |
Acute Kidney Tubular Necrosis [description not available] | 0 | 4.71 | 2 | 1 |
Kidney Tubular Necrosis, Acute Acute kidney failure resulting from destruction of EPITHELIAL CELLS of the KIDNEY TUBULES. It is commonly attributed to exposure to toxic agents or renal ISCHEMIA following severe TRAUMA. | 0 | 4.71 | 2 | 1 |
Articulation Disorders Disorders of the quality of speech characterized by the substitution, omission, distortion, and addition of phonemes. | 0 | 2.04 | 1 | 0 |
Familial Spastic Paraparesis, Htlv-1-Associated [description not available] | 0 | 2.42 | 2 | 0 |
Leukemia, Lymphocytic, Chronic, T Cell [description not available] | 0 | 2.04 | 1 | 0 |
Leukemia, Prolymphocytic, T-Cell A lymphoid leukemia characterized by a profound LYMPHOCYTOSIS with or without LYMPHADENOPATHY, hepatosplenomegaly, frequently rapid progression, and short survival. It was formerly called T-cell chronic lymphocytic leukemia. | 0 | 2.04 | 1 | 0 |
Paraparesis, Tropical Spastic A subacute paralytic myeloneuropathy occurring endemically in tropical areas such as the Caribbean, Colombia, India, and Africa, as well as in the southwestern region of Japan; associated with infection by HUMAN T-CELL LEUKEMIA VIRUS I. Clinical manifestations include a slowly progressive spastic weakness of the legs, increased reflexes, Babinski signs, incontinence, and loss of vibratory and position sensation. On pathologic examination inflammatory, demyelination, and necrotic lesions may be found in the spinal cord. (Adams et al., Principles of Neurology, 6th ed, p1239) | 0 | 2.42 | 2 | 0 |
Kidney, Polycystic [description not available] | 0 | 2.69 | 3 | 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 | 2.69 | 3 | 0 |
Encephalopathy, Hypertensive [description not available] | 0 | 2.04 | 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 | 2.42 | 2 | 0 |
Cardiovascular Tuberculosis [description not available] | 0 | 2.04 | 1 | 0 |
Amnesia, Anterograde Loss of the ability to form new memories beyond a certain point in time. This condition may be organic or psychogenic in origin. Organically induced anterograde amnesia may follow CRANIOCEREBRAL TRAUMA; SEIZURES; ANOXIA; and other conditions which adversely affect neural structures associated with memory formation (e.g., the HIPPOCAMPUS; FORNIX (BRAIN); MAMMILLARY BODIES; and ANTERIOR THALAMIC NUCLEI). (From Memory 1997 Jan-Mar;5(1-2):49-71) | 0 | 2.04 | 1 | 0 |
Cerebral Cortical Dysplasia [description not available] | 0 | 2.04 | 1 | 0 |
Ascites, Gelatinous [description not available] | 0 | 2.42 | 2 | 0 |
Pseudomyxoma Peritonei A peritoneal adenocarcinoma characterized by build-up of MUCUS in the PERITONEAL CAVITY. Mucus secreting cells may attach to the peritoneal lining and continue to secrete mucus. The majority of cases represent tumor spread from a primary low-grade mucinous neoplasm of the APPENDIX (NCI Thesaurus). | 0 | 2.42 | 2 | 0 |
Dizzyness [description not available] | 0 | 2.92 | 4 | 0 |
Dizziness An imprecise term which may refer to a sense of spatial disorientation, motion of the environment, or lightheadedness. | 0 | 2.92 | 4 | 0 |
Astrocytosis [description not available] | 0 | 3.62 | 3 | 0 |
Adenocarcinoma, Alveolar [description not available] | 0 | 2.96 | 1 | 0 |
Coin Lesion, Pulmonary [description not available] | 0 | 3.33 | 2 | 0 |
Adenocarcinoma, Bronchiolo-Alveolar A carcinoma derived from epithelium of terminal bronchioles, in which the neoplastic tissue extends along the alveolar walls and grows in small masses within the alveoli. Involvement may be uniformly diffuse and massive, or nodular, or lobular. The neoplastic cells are cuboidal or columnar and form papillary structures. Mucin may be demonstrated in some of the cells and in the material in the alveoli, which also includes denuded cells. Metastases in regional lymph nodes, and in even more distant sites, are known to occur, but are infrequent. (From Stedman, 25th ed) | 0 | 2.96 | 1 | 0 |
Pneumonia, Pneumococcal A febrile disease caused by STREPTOCOCCUS PNEUMONIAE. | 0 | 2.96 | 1 | 0 |
Cutaneous Fistula An abnormal passage or communication leading from an internal organ to the surface of the body. | 0 | 2.96 | 1 | 0 |
Carcinoma, Bronchial [description not available] | 0 | 2.37 | 2 | 0 |
Cystadenocarcinoma A malignant neoplasm derived from glandular epithelium, in which cystic accumulations of retained secretions are formed. The neoplastic cells manifest varying degrees of anaplasia and invasiveness, and local extension and metastases occur. Cystadenocarcinomas develop frequently in the ovaries, where pseudomucinous and serous types are recognized. (Stedman, 25th ed) | 0 | 2.67 | 3 | 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 | 2.37 | 2 | 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 | 4.27 | 4 | 1 |
Bone Loss, Osteoclastic [description not available] | 0 | 4.47 | 5 | 1 |
Acquired-Immune Deficiency Syndrome Dementia Complex [description not available] | 0 | 3.99 | 5 | 0 |
AIDS Dementia Complex A neurologic condition associated with the ACQUIRED IMMUNODEFICIENCY SYNDROME and characterized by impaired concentration and memory, slowness of hand movements, ATAXIA, incontinence, apathy, and gait difficulties associated with HIV-1 viral infection of the central nervous system. Pathologic examination of the brain reveals white matter rarefaction, perivascular infiltrates of lymphocytes, foamy macrophages, and multinucleated giant cells. (From Adams et al., Principles of Neurology, 6th ed, pp760-1; N Engl J Med, 1995 Apr 6;332(14):934-40) | 0 | 3.99 | 5 | 0 |
Infections, Soft Tissue [description not available] | 0 | 4 | 5 | 0 |
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 | 4 | 5 | 0 |
Autoimmune Demyelinating Disease, Peripheral [description not available] | 0 | 3.24 | 6 | 0 |
Gammapathy, Monoclonal [description not available] | 0 | 2.39 | 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 | 2.39 | 2 | 0 |
Osteosclerosis An abnormal hardening or increased density of bone tissue. | 0 | 2.9 | 1 | 0 |
Rida [description not available] | 0 | 2.39 | 2 | 0 |
Apoplexy, Pituitary [description not available] | 0 | 1.98 | 1 | 0 |
Asphyxia Neonatorum Respiratory failure in the newborn. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Anoxia, Brain [description not available] | 0 | 1.98 | 1 | 0 |
Aspiration, Meconium [description not available] | 0 | 1.98 | 1 | 0 |
Meconium Aspiration Syndrome A condition caused by inhalation of MECONIUM into the LUNG of FETUS or NEWBORN, usually due to vigorous respiratory movements during difficult PARTURITION or respiratory system abnormalities. Meconium aspirate may block small airways leading to difficulties in PULMONARY GAS EXCHANGE and ASPIRATION PNEUMONIA. | 0 | 1.98 | 1 | 0 |
Anus Diseases Diseases involving the ANUS. | 0 | 2.9 | 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 | 3.3 | 2 | 0 |
Abscess, Abdominal [description not available] | 0 | 3.78 | 2 | 1 |
Abdominal Abscess An abscess located in the abdominal cavity, i.e., the cavity between the diaphragm above and the pelvis below. (From Dorland, 27th ed) | 0 | 3.78 | 2 | 1 |
Multiple Neurofibromas [description not available] | 0 | 3.31 | 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 | 3.31 | 2 | 0 |
Island Cell Tumor [description not available] | 0 | 3.82 | 4 | 0 |
Adenoma, Islet Cell A benign tumor of the pancreatic ISLET CELLS. Usually it involves the INSULIN-producing PANCREATIC BETA CELLS, as in INSULINOMA, resulting in HYPERINSULINISM. | 0 | 3.82 | 4 | 0 |
Mast Cell Activation Disease [description not available] | 0 | 2.39 | 2 | 0 |
Mastocytosis A rare neoplastic disorder characterized by a clonal proliferation of MAST CELLS, associated with KIT-D816 mutations, and accompanied by aberrant mast cell activation. The abnormal increase of MAST CELLS may occur in only the skin (MASTOCYTOSIS, CUTANEOUS), in extracutaneous tissues involving multiple organs (MASTOCYTOSIS, SYSTEMIC), or in solid tumors (MASTOCYTOMA). | 0 | 2.39 | 2 | 0 |
Fracture, Pathologic [description not available] | 0 | 7.48 | 9 | 0 |
Diffuse Tenosynovial Giant Cell Tumor [description not available] | 0 | 1.98 | 1 | 0 |
Synovitis, Pigmented Villonodular Diffuse outgrowth arising from the SYNOVIAL MEMBRANE; SYNOVIAL BURSA; or TENDON sheath around the joint cavity, with extension to surrounding soft tissue. It is characterized by pigmented HEMOSIDERIN-containing MACROPHAGES; FOAM CELLS; and multinucleated GIANT CELLS. It usually occurs in the hands and feet, and around large joints, such as in the ankle and knee joints. | 0 | 1.98 | 1 | 0 |
Hypospermatogenesis [description not available] | 0 | 2.9 | 1 | 0 |
Varicocele A condition characterized by the dilated tortuous veins of the SPERMATIC CORD with a marked left-sided predominance. Adverse effect on male fertility occurs when varicocele leads to an increased scrotal (and testicular) temperature and reduced testicular volume. | 0 | 2.9 | 1 | 0 |
Alcoholic Liver Diseases [description not available] | 0 | 2.9 | 4 | 0 |
Liver Diseases, Alcoholic Liver diseases associated with ALCOHOLISM. It usually refers to the coexistence of two or more subentities, i.e., ALCOHOLIC FATTY LIVER; ALCOHOLIC HEPATITIS; and ALCOHOLIC CIRRHOSIS. | 0 | 2.9 | 4 | 0 |
Grippe [description not available] | 0 | 2.9 | 1 | 0 |
Influenza, Human An acute viral infection in humans involving the respiratory tract. It is marked by inflammation of the NASAL MUCOSA; the PHARYNX; and conjunctiva, and by headache and severe, often generalized, myalgia. | 0 | 2.9 | 1 | 0 |
Meniscitis [description not available] | 0 | 1.98 | 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 | 2.89 | 4 | 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 | 2.9 | 4 | 0 |
Abscess, Intracranial, Subdural [description not available] | 0 | 2.68 | 3 | 0 |
Autosomal Recessive Chronic Granulomatous Disease [description not available] | 0 | 1.98 | 1 | 0 |
Bone Inflammation [description not available] | 0 | 2.4 | 2 | 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 | 1.98 | 1 | 0 |
Conjunctival Neoplasms Tumors or cancer of the CONJUNCTIVA. | 0 | 2.9 | 1 | 0 |
Pseudarthrosis A pathologic entity characterized by deossification of a weight-bearing long bone, followed by bending and pathologic fracture, with inability to form normal BONY CALLUS leading to existence of the false joint that gives the condition its name. (Dorland, 27th ed) | 0 | 1.98 | 1 | 0 |
Argentaffinoma [description not available] | 0 | 4.29 | 4 | 0 |
Diarrheogenic Islet Cell Tumor [description not available] | 0 | 1.98 | 1 | 0 |
Gastrin-Producing Tumor [description not available] | 0 | 1.98 | 1 | 0 |
Carcinoid Tumor A usually small, slow-growing neoplasm composed of islands of rounded, oxyphilic, or spindle-shaped cells of medium size, with moderately small vesicular nuclei, and covered by intact mucosa with a yellow cut surface. The tumor can occur anywhere in the gastrointestinal tract (and in the lungs and other sites); approximately 90% arise in the appendix. It is now established that these tumors are of neuroendocrine origin and derive from a primitive stem cell. (From Stedman, 25th ed & Holland et al., Cancer Medicine, 3d ed, p1182) | 0 | 4.29 | 4 | 0 |
Gastrinoma A GASTRIN-secreting neuroendocrine tumor of the non-beta ISLET CELLS, the GASTRIN-SECRETING CELLS. This type of tumor is primarily located in the PANCREAS or the DUODENUM. Majority of gastrinomas are malignant. They metastasize to the LIVER; LYMPH NODES; and BONE but rarely elsewhere. The presence of gastrinoma is one of three requirements to be met for identification of ZOLLINGER-ELLISON SYNDROME, which sometimes occurs in families with MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; (MEN 1). | 0 | 1.98 | 1 | 0 |
Neoplasm Metastasis, Unknown Primary [description not available] | 0 | 2.89 | 4 | 0 |
Distorted Hearing [description not available] | 0 | 2.68 | 3 | 0 |
Retinal Diseases Diseases involving the RETINA. | 0 | 3.23 | 6 | 0 |
Epiphora [description not available] | 0 | 2.67 | 3 | 0 |
Lacrimal Apparatus Diseases Diseases of the LACRIMAL APPARATUS. | 0 | 2.67 | 3 | 0 |
Optic Atrophy Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition. | 0 | 1.98 | 1 | 0 |
Brain Embolism and Thrombosis [description not available] | 0 | 3.08 | 5 | 0 |
Syndrome, VKH (Vogt Koyanagi Harada) [description not available] | 0 | 1.98 | 1 | 0 |
Uveomeningoencephalitic Syndrome A syndrome characterized by bilateral granulomatous UVEITIS with IRITIS and secondary GLAUCOMA, premature ALOPECIA, symmetrical VITILIGO, poliosis circumscripta (a strand of depigmented hair), HEARING DISORDERS, and meningeal signs (neck stiffness and headache). Examination of the cerebrospinal fluid reveals a pattern consistent with MENINGITIS, ASEPTIC. (Adams et al., Principles of Neurology, 6th ed, p748; Surv Ophthalmol 1995 Jan;39(4):265-292) | 0 | 1.98 | 1 | 0 |
Middle Ear Inflammation [description not available] | 0 | 3.81 | 4 | 0 |
Otitis Media Inflammation of the MIDDLE EAR including the AUDITORY OSSICLES and the EUSTACHIAN TUBE. | 0 | 3.81 | 4 | 0 |
Neoplasms, Bronchial [description not available] | 0 | 2.39 | 2 | 0 |
Bronchial Neoplasms Tumors or cancer of the BRONCHI. | 0 | 2.39 | 2 | 0 |
Neoplasms, Otorhinolaryngologic [description not available] | 0 | 1.98 | 1 | 0 |
Ankylosing Spondylarthritis [description not available] | 0 | 3.78 | 2 | 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 | 3.78 | 2 | 1 |
Creeping Eruption [description not available] | 0 | 1.98 | 1 | 0 |
Cancer of Larynx [description not available] | 0 | 3.08 | 5 | 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 | 3.08 | 5 | 0 |
Cancer of Salivary Gland [description not available] | 0 | 2.39 | 2 | 0 |
Salivary Gland Neoplasms Tumors or cancer of the SALIVARY GLANDS. | 0 | 2.39 | 2 | 0 |
Thyroid Nodule A small circumscribed mass in the THYROID GLAND that can be of neoplastic growth or non-neoplastic abnormality. It lacks a well-defined capsule or glandular architecture. Thyroid nodules are often benign but can be malignant. The growth of nodules can lead to a multinodular goiter (GOITER, NODULAR). | 0 | 1.98 | 1 | 0 |
Hemarthrosis Bleeding into the joints. It may arise from trauma or spontaneously in patients with hemophilia. | 0 | 1.98 | 1 | 0 |
Intertrochanteric Fractures [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Pus [description not available] | 0 | 2.9 | 4 | 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 |
Zollinger-Ellison Syndrome A syndrome that is characterized by the triad of severe PEPTIC ULCER, hypersecretion of GASTRIC ACID, and GASTRIN-producing tumors of the PANCREAS or other tissue (GASTRINOMA). This syndrome may be sporadic or be associated with MULTIPLE ENDOCRINE NEOPLASIA TYPE 1. | 0 | 1.98 | 1 | 0 |
Adenofibroma A benign neoplasm composed of glandular and fibrous tissues, with a relatively large proportion of glands. (Stedman, 25th ed) | 0 | 3.3 | 2 | 0 |
Chronic Primary Open Angle Glaucoma [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Neoplasms, Nerve Tissue Neoplasms composed of nerve tissue. This concept does not refer to neoplasms located in the nervous system or its component nerves. | 0 | 3.76 | 2 | 1 |
Eaton-Lambert Myasthenic Syndrome [description not available] | 0 | 1.98 | 1 | 0 |
Lambert-Eaton Myasthenic Syndrome An autoimmune disease characterized by weakness and fatigability of proximal muscles, particularly of the pelvic girdle, lower extremities, trunk, and shoulder girdle. There is relative sparing of extraocular and bulbar muscles. CARCINOMA, SMALL CELL of the lung is a frequently associated condition, although other malignancies and autoimmune diseases may be associated. Muscular weakness results from impaired impulse transmission at the NEUROMUSCULAR JUNCTION. Presynaptic calcium channel dysfunction leads to a reduced amount of acetylcholine being released in response to stimulation of the nerve. (From Adams et al., Principles of Neurology, 6th ed, pp 1471) | 0 | 1.98 | 1 | 0 |
Granulocytic Leukemia [description not available] | 0 | 1.98 | 1 | 0 |
Leukemia, Myeloid Form of leukemia characterized by an uncontrolled proliferation of the myeloid lineage and their precursors (MYELOID PROGENITOR CELLS) in the bone marrow and other sites. | 0 | 1.98 | 1 | 0 |
Tuberculosis, Miliary An acute form of TUBERCULOSIS in which minute tubercles are formed in a number of organs of the body due to dissemination of the bacilli through the blood stream. | 0 | 2.38 | 2 | 0 |
Genital Herpes [description not available] | 0 | 1.98 | 1 | 0 |
Herpes Simplex Virus Infection [description not available] | 0 | 2.69 | 3 | 0 |
Herpes Genitalis Infection of the genitals (GENITALIA) with HERPES SIMPLEX VIRUS in either the males or the females. | 0 | 1.98 | 1 | 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 | 2.69 | 3 | 0 |
Foreign Bodies Inanimate objects that become enclosed in the body. | 0 | 1.98 | 1 | 0 |
Dementia Praecox [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Acne [description not available] | 0 | 1.98 | 1 | 0 |
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 | 1.98 | 1 | 0 |
Periphlebitis Periphlebitis is inflammation of the outer coat of a vein or of tissues surrounding the vein. | 0 | 3.79 | 2 | 1 |
Phlebitis Inflammation of a vein, often a vein in the leg. Phlebitis associated with a blood clot is called (THROMBOPHLEBITIS). | 0 | 3.79 | 2 | 1 |
Nevi, Intradermal [description not available] | 0 | 1.98 | 1 | 0 |
Nevi, Melanocytic [description not available] | 0 | 1.98 | 1 | 0 |
Blue Nevi [description not available] | 0 | 1.98 | 1 | 0 |
Nevus, Pigmented A nevus containing melanin. The term is usually restricted to nevocytic nevi (round or oval collections of melanin-containing nevus cells occurring at the dermoepidermal junction of the skin or in the dermis proper) or moles, but may be applied to other pigmented nevi. | 0 | 1.98 | 1 | 0 |
Muscle Spasm [description not available] | 0 | 3.3 | 2 | 0 |
Spasm An involuntary contraction of a muscle or group of muscles. Spasms may involve SKELETAL MUSCLE or SMOOTH MUSCLE. | 0 | 3.3 | 2 | 0 |
Aneurysm, Bacterial [description not available] | 0 | 2.9 | 1 | 0 |
Fat Necrosis A condition in which the death of adipose tissue results in neutral fats being split into fatty acids and glycerol. | 0 | 2.39 | 2 | 0 |
Foreign-Body Reaction Chronic inflammation and granuloma formation around irritating foreign bodies. | 0 | 1.99 | 1 | 0 |
Aneuploid [description not available] | 0 | 2.39 | 2 | 0 |
Adrenal Gland Diseases Pathological processes of the ADRENAL GLANDS. | 0 | 4.7 | 2 | 1 |
Common Bile Duct Diseases Diseases of the COMMON BILE DUCT including the AMPULLA OF VATER and the SPHINCTER OF ODDI. | 0 | 1.99 | 1 | 0 |
Milk-Alkali Syndrome [description not available] | 0 | 2.39 | 2 | 0 |
Hypercalcemia Abnormally high level of calcium in the blood. | 0 | 2.39 | 2 | 0 |
Papilloma, Squamous Cell [description not available] | 0 | 3.3 | 2 | 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 | 8.3 | 2 | 0 |
Cherubism A fibro-osseous hereditary disease of the jaws. The swollen jaws and raised eyes give a cherubic appearance; multiple radiolucencies are evident upon radiographic examination. | 0 | 2.9 | 1 | 0 |
Breast Cancer, Male [description not available] | 0 | 2.9 | 1 | 0 |
Breast Neoplasms, Male Any neoplasms of the male breast. These occur infrequently in males in developed countries, the incidence being about 1% of that in females. | 0 | 2.9 | 1 | 0 |
Benign Frontal Childhood Epilepsy [description not available] | 0 | 1.99 | 1 | 0 |
Hair Diseases Diseases affecting the orderly growth and persistence of hair. | 0 | 1.99 | 1 | 0 |
Benign Pilomatricoma [description not available] | 0 | 1.99 | 1 | 0 |
Microglossia [description not available] | 0 | 2.39 | 2 | 0 |
Cranial Epidural Hematoma [description not available] | 0 | 2.68 | 3 | 0 |
Myoglobinuria The presence of MYOGLOBIN in URINE usually as a result of rhabdomyolysis. | 0 | 2.39 | 2 | 0 |
Clear Cell Sarcoma of Soft Tissue [description not available] | 0 | 1.99 | 1 | 0 |
Sarcoma, Clear Cell A sarcoma of young adults occurring in the lower extremities and acral regions. It is found intimately bound to tendons as a circumscribed but unencapsulated melanin-bearing tumor of neuroectodermal origin. Clear cell sarcoma is associated with a specific t(12;22)(q13;q12) translocation. | 0 | 1.99 | 1 | 0 |
Cystic Hygroma Colli [description not available] | 0 | 2.9 | 1 | 0 |
Chorioadenoma [description not available] | 0 | 1.99 | 1 | 0 |
Hydatid Mole [description not available] | 0 | 1.99 | 1 | 0 |
Neoplasms, Trophoblastic [description not available] | 0 | 1.99 | 1 | 0 |
Hydatidiform Mole Trophoblastic hyperplasia associated with normal gestation, or molar pregnancy. It is characterized by the swelling of the CHORIONIC VILLI and elevated human CHORIONIC GONADOTROPIN. Hydatidiform moles or molar pregnancy may be categorized as complete or partial based on their gross morphology, histopathology, and karyotype. | 0 | 1.99 | 1 | 0 |
Encephalopathy, Hepatic [description not available] | 0 | 1.99 | 1 | 0 |
Hepatic Encephalopathy A syndrome characterized by central nervous system dysfunction in association with LIVER FAILURE, including portal-systemic shunts. Clinical features include lethargy and CONFUSION (frequently progressing to COMA); ASTERIXIS; NYSTAGMUS, PATHOLOGIC; brisk oculovestibular reflexes; decorticate and decerebrate posturing; MUSCLE SPASTICITY; and bilateral extensor plantar reflexes (see REFLEX, BABINSKI). ELECTROENCEPHALOGRAPHY may demonstrate triphasic waves. (From Adams et al., Principles of Neurology, 6th ed, pp1117-20; Plum & Posner, Diagnosis of Stupor and Coma, 3rd ed, p222-5) | 0 | 1.99 | 1 | 0 |
Primate Diseases Diseases of animals within the order PRIMATES. This term includes diseases of Haplorhini and Strepsirhini. | 0 | 1.99 | 1 | 0 |
Coenuri Infection [description not available] | 0 | 3.31 | 2 | 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 | 3.31 | 2 | 0 |
Coccidioides immitis Infection [description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Infections, Listeria [description not available] | 0 | 1.99 | 1 | 0 |
Abscess, Hepatic [description not available] | 0 | 3.23 | 6 | 0 |
Liver Abscess Solitary or multiple collections of PUS within the liver as a result of infection by bacteria, protozoa, or other agents. | 0 | 8.23 | 6 | 0 |
Phlegmon [description not available] | 0 | 4.48 | 5 | 1 |
Mouth Diseases Diseases involving the MOUTH. | 0 | 1.99 | 1 | 0 |
Cellulitis An acute, diffuse, and suppurative inflammation of loose connective tissue, particularly the deep subcutaneous tissues, and sometimes muscle, which is most commonly seen as a result of infection of a wound, ulcer, or other skin lesions. | 0 | 4.48 | 5 | 1 |
Mesenteric Vascular Occlusion Obstruction of the flow in the SPLANCHNIC CIRCULATION by ATHEROSCLEROSIS; EMBOLISM; THROMBOSIS; STENOSIS; TRAUMA; and compression or intrinsic pressure from adjacent tumors. Rare causes are drugs, intestinal parasites, and vascular immunoinflammatory diseases such as PERIARTERITIS NODOSA and THROMBOANGIITIS OBLITERANS. (From Juergens et al., Peripheral Vascular Diseases, 5th ed, pp295-6) | 0 | 3.1 | 5 | 0 |
Generalized Resistance to Thyroid Hormone [description not available] | 0 | 1.99 | 1 | 0 |
Connective Tissue Neoplasms [description not available] | 0 | 1.99 | 1 | 0 |
Pink Eye [description not available] | 0 | 1.99 | 1 | 0 |
Conjunctivitis INFLAMMATION of the CONJUNCTIVA. | 0 | 1.99 | 1 | 0 |
Hyperprolactinaemia [description not available] | 0 | 2.68 | 3 | 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 | 2.68 | 3 | 0 |
Inappropriate GH Secretion Syndrome (Acromegaly) [description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Fasciitis, Necrotizing A fulminating bacterial infection of the deep layers of the skin and FASCIA. It can be caused by many different organisms, with STREPTOCOCCUS PYOGENES being the most common. | 0 | 1.99 | 1 | 0 |
SC Disease [description not available] | 0 | 1.99 | 1 | 0 |
Hemoglobin SC Disease One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia. | 0 | 1.99 | 1 | 0 |
Colonic Diseases Pathological processes in the COLON region of the large intestine (INTESTINE, LARGE). | 0 | 2.39 | 2 | 0 |
Hyperesthesia Increased sensitivity to cutaneous stimulation due to a diminished threshold or an increased response to stimuli. | 0 | 1.99 | 1 | 0 |
Anterior Horn Cell Disease [description not available] | 0 | 1.99 | 1 | 0 |
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 | 1.99 | 1 | 0 |
Phlegmasia Alba Dolens Inflammation that is characterized by swollen, pale, and painful limb. It is usually caused by DEEP VEIN THROMBOSIS in a FEMORAL VEIN, following PARTURITION or an illness. This condition is also called milk leg or white leg. | 0 | 2.68 | 3 | 0 |
Thrombophlebitis Inflammation of a vein associated with a blood clot (THROMBUS). | 0 | 7.68 | 3 | 0 |
Adenoma, Villous An adenoma of the large intestine. It is usually a solitary, sessile, often large, tumor of colonic mucosa composed of mucinous epithelium covering delicate vascular projections. Hypersecretion and malignant changes occur frequently. (Stedman, 25th ed) | 0 | 1.99 | 1 | 0 |
Apnea A transient absence of spontaneous respiration. | 0 | 3.78 | 2 | 1 |
Bowel Incontinence [description not available] | 0 | 1.99 | 1 | 0 |
Fecal Incontinence Failure of voluntary control of the anal sphincters, with involuntary passage of feces and flatus. | 0 | 1.99 | 1 | 0 |
Dehydration The condition that results from excessive loss of water from a living organism. | 0 | 1.99 | 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 | 1.99 | 1 | 0 |
Angina Pectoris with Normal Coronary Arteriogram [description not available] | 0 | 2.91 | 1 | 0 |
Injuries, Eye [description not available] | 0 | 1.99 | 1 | 0 |
Eye Injuries Damage or trauma inflicted to the eye by external means. The concept includes both surface injuries and intraocular injuries. | 0 | 1.99 | 1 | 0 |
Asymmetric Diabetic Proximal Motor Neuropathy [description not available] | 0 | 1.99 | 1 | 0 |
Diabetic Neuropathies Peripheral, autonomic, and cranial nerve disorders that are associated with DIABETES MELLITUS. These conditions usually result from diabetic microvascular injury involving small blood vessels that supply nerves (VASA NERVORUM). Relatively common conditions which may be associated with diabetic neuropathy include third nerve palsy (see OCULOMOTOR NERVE DISEASES); MONONEUROPATHY; mononeuropathy multiplex; diabetic amyotrophy; a painful POLYNEUROPATHY; autonomic neuropathy; and thoracoabdominal neuropathy. (From Adams et al., Principles of Neurology, 6th ed, p1325) | 0 | 1.99 | 1 | 0 |
Myelolipoma A rare benign tumor of the adrenal gland, several centimeters in diameter, composed in varying proportions of adipose tissue, lymphocytes, and primitive myeloid cells, probably a developmental abnormality. (Dorland, 27th ed) | 0 | 1.99 | 1 | 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 | 2.91 | 1 | 0 |
T-Cell Lymphoma [description not available] | 0 | 1.99 | 1 | 0 |
Lymphoma, T-Cell A group of heterogeneous lymphoid tumors representing malignant transformations of T-lymphocytes. | 0 | 1.99 | 1 | 0 |
Bacterial Skin Diseases [description not available] | 0 | 2.91 | 1 | 0 |
Skin Diseases, Bacterial Skin diseases caused by bacteria. | 0 | 2.91 | 1 | 0 |
Anaplasia Loss of structural differentiation and useful function of neoplastic cells. | 0 | 1.99 | 1 | 0 |
Bone Tuberculosis [description not available] | 0 | 3.32 | 2 | 0 |
Impotence [description not available] | 0 | 6.99 | 1 | 0 |
Erectile Dysfunction The inability in the male to have a PENILE ERECTION due to psychological or organ dysfunction. | 0 | 1.99 | 1 | 0 |
Breathing Sounds [description not available] | 0 | 1.99 | 1 | 0 |
Tracheal Neoplasms New abnormal growth of tissue in the TRACHEA. | 0 | 1.99 | 1 | 0 |
Respiratory Sounds Noises, normal and abnormal, heard on auscultation over any part of the RESPIRATORY TRACT. | 0 | 1.99 | 1 | 0 |
Anterior Ischemic Optic Neuropathy [description not available] | 0 | 1.99 | 1 | 0 |
Optic Neuropathy, Ischemic Ischemic injury to the OPTIC NERVE which usually affects the OPTIC DISK (optic neuropathy, anterior ischemic) and less frequently the retrobulbar portion of the nerve (optic neuropathy, posterior ischemic). The injury results from occlusion of arterial blood supply which may result from TEMPORAL ARTERITIS; ATHEROSCLEROSIS; COLLAGEN DISEASES; EMBOLISM; DIABETES MELLITUS; and other conditions. The disease primarily occurs in the sixth decade or later and presents with the sudden onset of painless and usually severe monocular visual loss. Anterior ischemic optic neuropathy also features optic disk edema with microhemorrhages. The optic disk appears normal in posterior ischemic optic neuropathy. (Glaser, Neuro-Ophthalmology, 2nd ed, p135) | 0 | 1.99 | 1 | 0 |
Acroosteolysis, Giaccai Type [description not available] | 0 | 1.99 | 1 | 0 |
Hereditary Sensory and Autonomic Neuropathies A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4) | 0 | 1.99 | 1 | 0 |
Genital Diseases, Male Pathological processes involving the male reproductive tract (GENITALIA, MALE). | 0 | 2.39 | 2 | 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 | 1.99 | 1 | 0 |
Bone Diseases, Infectious Bone diseases caused by pathogenic microorganisms. | 0 | 1.99 | 1 | 0 |
Affective Disorders [description not available] | 0 | 1.99 | 1 | 0 |
Mood Disorders Those disorders that have a disturbance in mood as their predominant feature. | 0 | 1.99 | 1 | 0 |
Dyskinesia, Medication-Induced [description not available] | 0 | 1.99 | 1 | 0 |
Dyskinesia, Drug-Induced Abnormal movements, including HYPERKINESIS; HYPOKINESIA; TREMOR; and DYSTONIA, associated with the use of certain medications or drugs. Muscles of the face, trunk, neck, and extremities are most commonly affected. Tardive dyskinesia refers to abnormal hyperkinetic movements of the muscles of the face, tongue, and neck associated with the use of neuroleptic agents (see ANTIPSYCHOTIC AGENTS). (Adams et al., Principles of Neurology, 6th ed, p1199) | 0 | 1.99 | 1 | 0 |
Neuroretinitis [description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Retinitis Inflammation of the RETINA. It is rarely limited to the retina, but is commonly associated with diseases of the choroid (CHORIORETINITIS) and of the OPTIC DISK (neuroretinitis). | 0 | 6.99 | 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 | 2.4 | 2 | 0 |
Cancer of Pharynx [description not available] | 0 | 2.9 | 4 | 0 |
Kaposi Sarcoma [description not available] | 0 | 2.67 | 3 | 0 |
Conductive Hearing Loss [description not available] | 0 | 1.99 | 1 | 0 |
Pharyngeal Neoplasms Tumors or cancer of the PHARYNX. | 0 | 2.9 | 4 | 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 | 2.67 | 3 | 0 |
Idiopathic Parkinson Disease [description not available] | 0 | 3.31 | 2 | 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 | 3.31 | 2 | 0 |
Coagulation, Disseminated Intravascular [description not available] | 0 | 1.99 | 1 | 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 | 1.99 | 1 | 0 |
Algodystrophic Syndrome [description not available] | 0 | 2.68 | 3 | 0 |
Reflex Sympathetic Dystrophy A syndrome characterized by severe burning pain in an extremity accompanied by sudomotor, vasomotor, and trophic changes in bone without an associated specific nerve injury. This condition is most often precipitated by trauma to soft tissue or nerve complexes. The skin over the affected region is usually erythematous and demonstrates hypersensitivity to tactile stimuli and erythema. (Adams et al., Principles of Neurology, 6th ed, p1360; Pain 1995 Oct;63(1):127-33) | 0 | 2.68 | 3 | 0 |
Granuloma Annulare Benign granulomatous disease of unknown etiology characterized by a ring of localized or disseminated papules or nodules on the skin and palisading histiocytes surrounding necrobiotic tissue resulting from altered collagen structures. | 0 | 1.99 | 1 | 0 |
Hand Dermatosis [description not available] | 0 | 1.99 | 1 | 0 |
Foot Dermatoses Skin diseases of the foot, general or unspecified. | 0 | 1.99 | 1 | 0 |
Hand Dermatoses Skin diseases involving the HANDS. | 0 | 1.99 | 1 | 0 |
Closed Head Injuries [description not available] | 0 | 1.99 | 1 | 0 |
Synovioma [description not available] | 0 | 3.59 | 3 | 0 |
Sarcoma, Synovial A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363) | 0 | 3.59 | 3 | 0 |
Ovine Diseases [description not available] | 0 | 1.99 | 1 | 0 |
Infections, Lentivirus [description not available] | 0 | 1.99 | 1 | 0 |
Hypesthesia Absent or reduced sensitivity to cutaneous stimulation. | 0 | 2.91 | 1 | 0 |
Neuritis A general term indicating inflammation of a peripheral or cranial nerve. Clinical manifestation may include PAIN; PARESTHESIAS; PARESIS; or HYPESTHESIA. | 0 | 8.3 | 2 | 0 |
Carcinoma, Embryonal A highly malignant, primitive form of carcinoma, probably of germinal cell or teratomatous derivation, usually arising in a gonad and rarely in other sites. It is rare in the female ovary, but in the male it accounts for 20% of all testicular tumors. (From Dorland, 27th ed & Holland et al., Cancer Medicine, 3d ed, p1595) | 0 | 1.99 | 1 | 0 |
Seminoma A radiosensitive, malignant neoplasm of the testis, thought to be derived from primordial germ cells of the sexually undifferentiated embryonic gonad. There are three variants: classical (typical), the most common type; anaplastic; and spermatocytic. The classical seminoma is composed of fairly well differentiated sheets or cords of uniform polygonal or round cells (seminoma cells), each cell having abundant clear cytoplasm, distinct cell membranes, a centrally placed round nucleus, and one or more nucleoli. In the female, a grossly and histologically identical neoplasm, known as dysgerminoma, occurs. (Dorland, 27th ed) | 0 | 1.99 | 1 | 0 |
Finger Injuries General or unspecified injuries involving the fingers. | 0 | 1.99 | 1 | 0 |
Plasma Cell Tumor [description not available] | 0 | 2.39 | 2 | 0 |
Plasmacytoma Any discrete, presumably solitary, mass of neoplastic PLASMA CELLS either in BONE MARROW or various extramedullary sites. | 0 | 2.39 | 2 | 0 |
Dysphagia [description not available] | 0 | 1.99 | 1 | 0 |
Branchial Cleft Cyst [description not available] | 0 | 1.99 | 1 | 0 |
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 | 1.99 | 1 | 0 |
Infection [description not available] | 0 | 2 | 1 | 0 |
Infections Invasion of the host organism by microorganisms or their toxins or by parasites that can cause pathological conditions or diseases. | 0 | 2 | 1 | 0 |
Gallstone Disease [description not available] | 0 | 2.4 | 2 | 0 |
Bile Duct Cysts [description not available] | 0 | 2 | 1 | 0 |
Cholangitis Inflammation of the biliary ductal system (BILE DUCTS); intrahepatic, extrahepatic, or both. | 0 | 2.41 | 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 |
Biliary Tract Cancer [description not available] | 0 | 2 | 1 | 0 |
Biliary Tract Neoplasms Tumors or cancer in the BILIARY TRACT including the BILE DUCTS and the GALLBLADDER. | 0 | 2 | 1 | 0 |
Cancer of Duodenum [description not available] | 0 | 2 | 1 | 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 |
Abdominal Cryptorchidism [description not available] | 0 | 4.35 | 2 | 2 |
Cells, Neoplasm Circulating [description not available] | 0 | 3.79 | 2 | 1 |
Aortitis Inflammation of the wall of the AORTA. | 0 | 2.4 | 2 | 0 |
Leriche Syndrome A condition caused by occlusion of terminal aorta, the primary branches of the ABDOMINAL AORTA, as in aortoiliac obstruction. Leriche syndrome usually occurs in males and is characterized by IMPOTENCE, absence of a pulse in the femoral arteries, weakness and numbness in the lower back, buttocks, hips, and lower limbs. | 0 | 2 | 1 | 0 |
Cranial Nerve I Diseases [description not available] | 0 | 2 | 1 | 0 |
Bone Hypertrophy [description not available] | 0 | 2 | 1 | 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 | 7 | 1 | 0 |
B Virus Infection [description not available] | 0 | 2.92 | 1 | 0 |
Alcoholic Intoxication An acute brain syndrome which results from the excessive ingestion of ETHANOL or ALCOHOLIC BEVERAGES. | 0 | 2 | 1 | 0 |
Gastric Outlet Obstruction The hindering of output from the STOMACH into the SMALL INTESTINE. This obstruction may be of mechanical or functional origin such as EDEMA from PEPTIC ULCER; NEOPLASMS; FOREIGN BODIES; or AGING. | 0 | 3.39 | 1 | 1 |
Bile Duct Obstruction, Extrahepatic [description not available] | 0 | 2 | 1 | 0 |
Ascariasis Infection by nematodes of the genus ASCARIS. Ingestion of infective eggs causes diarrhea and pneumonitis. Its distribution is more prevalent in areas of poor sanitation and where human feces are used for fertilizer. | 0 | 2 | 1 | 0 |
Classic Globoid Cell Leukodystrophy [description not available] | 0 | 2.39 | 2 | 0 |
Leukodystrophy, Globoid Cell An autosomal recessive metabolic disorder caused by a deficiency of GALACTOSYLCERAMIDASE leading to intralysosomal accumulation of galactolipids such as GALACTOSYLCERAMIDES and PSYCHOSINE. It is characterized by demyelination associated with large multinucleated globoid cells, predominantly involving the white matter of the central nervous system. The loss of MYELIN disrupts normal conduction of nerve impulses. | 0 | 2.39 | 2 | 0 |
Deficiency, Protein S [description not available] | 0 | 2 | 1 | 0 |
Corneal Angiogenesis [description not available] | 0 | 2 | 1 | 0 |
Corneal Neovascularization New blood vessels originating from the corneal blood vessels and extending from the limbus into the adjacent CORNEAL STROMA. Neovascularization in the superficial and/or deep corneal stroma is a sequel to numerous inflammatory diseases of the ocular anterior segment, such as TRACHOMA, viral interstitial KERATITIS, microbial KERATOCONJUNCTIVITIS, and the immune response elicited by CORNEAL TRANSPLANTATION. | 0 | 2 | 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 | 1 | 0 |
Ear Infection [description not available] | 0 | 2.39 | 2 | 0 |
Cholesteatoma A non-neoplastic mass of keratin-producing squamous EPITHELIUM, frequently occurring in the MENINGES; bones of the skull, and most commonly in the MIDDLE EAR and MASTOID region. Cholesteatoma can be congenital or acquired. Cholesteatoma is not a tumor nor is it associated with high CHOLESTEROL. | 0 | 3.81 | 4 | 0 |
Capillaria hepatica Infection [description not available] | 0 | 2 | 1 | 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 | 1 | 0 |
Dissecting Vertebral Artery Aneurysm [description not available] | 0 | 3.79 | 2 | 1 |
Ethmoid Sinusitis Inflammation of the NASAL MUCOSA in the ETHMOID SINUS. It may present itself as an acute (infectious) or chronic (allergic) condition. | 0 | 2.39 | 2 | 0 |
Sinusitis, Maxillary [description not available] | 0 | 2.39 | 2 | 0 |
Sinusitis, Sphenoid [description not available] | 0 | 2 | 1 | 0 |
Maxillary Sinusitis Inflammation of the NASAL MUCOSA in the MAXILLARY SINUS. In many cases, it is caused by an infection of the bacteria HAEMOPHILUS INFLUENZAE; STREPTOCOCCUS PNEUMONIAE; or STAPHYLOCOCCUS AUREUS. | 0 | 2.39 | 2 | 0 |
Arthritis, Post-Infectious [description not available] | 0 | 3.39 | 1 | 1 |
Arthritis, Reactive An aseptic, inflammatory arthritis developing secondary to a primary extra-articular infection, most typically of the GASTROINTESTINAL TRACT or UROGENITAL SYSTEM. The initiating trigger pathogens are usually SHIGELLA; SALMONELLA; YERSINIA; CAMPYLOBACTER; or CHLAMYDIA TRACHOMATIS. Reactive arthritis is strongly associated with HLA-B27 ANTIGEN. | 0 | 3.39 | 1 | 1 |
Fibrous Tissue Neoplasms [description not available] | 0 | 2.92 | 1 | 0 |
Myoepithelial Tumor [description not available] | 0 | 2 | 1 | 0 |
Myoepithelioma A usually benign tumor made up predominantly of myoepithelial cells. | 0 | 2 | 1 | 0 |
Cancer of the Urinary Tract [description not available] | 0 | 2 | 1 | 0 |
Acidosis, Respiratory Respiratory retention of carbon dioxide. It may be chronic or acute. | 0 | 2 | 1 | 0 |
Di Guglielmo Disease [description not available] | 0 | 2.39 | 2 | 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 | 2.39 | 2 | 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 | 2 | 1 | 0 |
Osteosarcoma, Juxtacortical A form of osteogenic sarcoma of relatively low malignancy, probably arising from the periosteum and initially involving cortical bone and adjacent connective tissue. It occurs in middle-aged as well as young adults and most commonly affects the lower part of the femoral shaft. (Stedman, 25th ed) | 0 | 2 | 1 | 0 |
Embolism, Fat Blocking of a blood vessel by fat deposits in the circulation. It is often seen after fractures of large bones or after administration of CORTICOSTEROIDS. | 0 | 2 | 1 | 0 |
Hematoma, Subdural, Chronic Accumulation of blood in the SUBDURAL SPACE with delayed onset of neurological symptoms. Symptoms may include loss of consciousness, severe HEADACHE, and deteriorating mental status. | 0 | 2 | 1 | 0 |
Lesion of Sciatic Nerve [description not available] | 0 | 3.8 | 2 | 1 |
Bagassosis A diffuse parenchymal lung disease caused by inhaled dust from processing SUGARCANE (bagasse), usually in the manufacturing of wallboard. | 0 | 2 | 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 | 1 | 0 |
Lacerations Torn, ragged, mangled wounds. | 0 | 2 | 1 | 0 |
Short Bowel Syndrome A malabsorption syndrome resulting from extensive operative resection of the SMALL INTESTINE, the absorptive region of the GASTROINTESTINAL TRACT. | 0 | 2.01 | 1 | 0 |
Alopecia Cicatrisata [description not available] | 0 | 3.39 | 1 | 1 |
Alopecia Absence of hair from areas where it is normally present. | 0 | 3.39 | 1 | 1 |
Aortitis, Syphilitic [description not available] | 0 | 2.01 | 1 | 0 |
Cancer of Sigmoid [description not available] | 0 | 2.01 | 1 | 0 |
Abscess, Periapical [description not available] | 0 | 2.01 | 1 | 0 |
African Lymphoma [description not available] | 0 | 2.39 | 2 | 0 |
Burkitt Lymphoma A form of undifferentiated malignant LYMPHOMA usually found in central Africa, but also reported in other parts of the world. It is commonly manifested as a large osteolytic lesion in the jaw or as an abdominal mass. B-cell antigens are expressed on the immature cells that make up the tumor in virtually all cases of Burkitt lymphoma. The Epstein-Barr virus (HERPESVIRUS 4, HUMAN) has been isolated from Burkitt lymphoma cases in Africa and it is implicated as the causative agent in these cases; however, most non-African cases are EBV-negative. | 0 | 2.39 | 2 | 0 |
Bronchospasm [description not available] | 0 | 2.01 | 1 | 0 |
Bronchial Spasm Spasmodic contraction of the smooth muscle of the bronchi. | 0 | 2.01 | 1 | 0 |
Chemical Dependence [description not available] | 0 | 2.01 | 1 | 0 |
Drug Withdrawal Symptoms [description not available] | 0 | 2.01 | 1 | 0 |
Substance Withdrawal Syndrome Physiological and psychological symptoms associated with withdrawal from the use of a drug after prolonged administration or habituation. The concept includes withdrawal from smoking or drinking, as well as withdrawal from an administered drug. | 0 | 2.01 | 1 | 0 |
Substance-Related Disorders Disorders related to substance use or abuse. | 0 | 2.01 | 1 | 0 |
Nelson Syndrome A syndrome characterized by HYPERPIGMENTATION, enlarging pituitary mass, visual defects secondary to compression of the OPTIC CHIASM, and elevated serum ACTH. It is caused by the expansion of an underlying ACTH-SECRETING PITUITARY ADENOMA that grows in the absence of feedback inhibition by adrenal CORTICOSTEROIDS, usually after ADRENALECTOMY. | 0 | 2.92 | 1 | 0 |
Hereditary Hemorrhagic Telangiectasia [description not available] | 0 | 2.01 | 1 | 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 | 2.01 | 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 | 2.01 | 1 | 0 |
Carcinoma, Oat Cell [description not available] | 0 | 2.89 | 4 | 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 | 2.89 | 4 | 0 |
Mucopolysaccharidosis [description not available] | 0 | 1.98 | 1 | 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 | 1.98 | 1 | 0 |
Cystosarcoma Phyllodes [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
ARC [description not available] | 0 | 1.98 | 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 | 1.98 | 1 | 0 |
Facial Neoplasms New abnormal growth of tissue in the FACE. | 0 | 1.98 | 1 | 0 |
Atelectasis [description not available] | 0 | 1.98 | 1 | 0 |
Varices [description not available] | 0 | 1.98 | 1 | 0 |
Varicose Veins Enlarged and tortuous VEINS. | 0 | 1.98 | 1 | 0 |
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 | 1.98 | 1 | 0 |
Hypercapnia A clinical manifestation of abnormal increase in the amount of carbon dioxide in arterial blood. | 0 | 1.98 | 1 | 0 |
Manganese Poisoning Manganese poisoning is associated with chronic inhalation of manganese particles by individuals who work with manganese ore. Clinical features include CONFUSION; HALLUCINATIONS; and an extrapyramidal syndrome (PARKINSON DISEASE, SECONDARY) that includes rigidity; DYSTONIA; retropulsion; and TREMOR. (Adams, Principles of Neurology, 6th ed, p1213) | 0 | 1.97 | 1 | 0 |
Iris Neoplasms Tumors of the iris characterized by increased pigmentation of melanocytes. Iris nevi are composed of proliferated melanocytes and are associated with neurofibromatosis and malignant melanoma of the choroid and ciliary body. Malignant melanoma of the iris often originates from preexisting nevi. | 0 | 1.97 | 1 | 0 |
Palatal Neoplasms Tumors or cancer of the PALATE, including those of the hard palate, soft palate and UVULA. | 0 | 1.97 | 1 | 0 |
Lymphangitis A lymphatic disease characterized by INFLAMMATION of LYMPHATIC VESSELS. | 0 | 1.97 | 1 | 0 |
Ectopic Ossification [description not available] | 0 | 1.97 | 1 | 0 |
Haemophilus Infections Infections with bacteria of the genus HAEMOPHILUS. | 0 | 1.97 | 1 | 0 |
Middle Ear Effusion [description not available] | 0 | 1.97 | 1 | 0 |
Infections, Pneumococcal [description not available] | 0 | 1.97 | 1 | 0 |
Otitis Media with Effusion Inflammation of the middle ear with a clear pale yellow-colored transudate. | 0 | 1.97 | 1 | 0 |
Pneumococcal Infections Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. | 0 | 1.97 | 1 | 0 |
Atypical Endometrial Hyperplasia A benign form of endometrial hyperplasia with increased number of cells with atypia. The atypical cells are large and irregular and have an increased nuclear/cytoplasmic ratio. The risk of progression to endometrial carcinoma rises with the increasing degree of cell atypia. | 0 | 1.97 | 1 | 0 |
Endometrial Hyperplasia Benign proliferation of the ENDOMETRIUM in the UTERUS. Endometrial hyperplasia is classified by its cytology and glandular tissue. There are simple, complex (adenomatous without atypia), and atypical hyperplasia representing also the ascending risk of becoming malignant. | 0 | 1.97 | 1 | 0 |
Parotid Diseases Diseases involving the PAROTID GLAND. | 0 | 2.38 | 2 | 0 |
Blood Vessel Tumors [description not available] | 0 | 1.97 | 1 | 0 |
Digestive System Disorders [description not available] | 0 | 1.97 | 1 | 0 |
Digestive System Diseases Diseases in any part of the GASTROINTESTINAL TRACT or the accessory organs (LIVER; BILIARY TRACT; PANCREAS). | 0 | 1.97 | 1 | 0 |
Paranasal Sinus Diseases Diseases affecting or involving the PARANASAL SINUSES and generally manifesting as inflammation, abscesses, cysts, or tumors. | 0 | 1.97 | 1 | 0 |
Femur Neck Fractures [description not available] | 0 | 6.78 | 4 | 0 |
Femoral Neck Fractures Fractures of the short, constricted portion of the thigh bone between the femur head and the trochanters. It excludes intertrochanteric fractures which are HIP FRACTURES. | 0 | 6.78 | 4 | 0 |
Osseous Paget's Disease [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Brittle Bone Disease [description not available] | 0 | 1.97 | 1 | 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 | 1.97 | 1 | 0 |
Hakim Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Hydrocephalus, Normal Pressure A form of compensated hydrocephalus characterized clinically by a slowly progressive gait disorder (see GAIT DISORDERS, NEUROLOGIC), progressive intellectual decline, and URINARY INCONTINENCE. Spinal fluid pressure tends to be in the high normal range. This condition may result from processes which interfere with the absorption of CSF including SUBARACHNOID HEMORRHAGE, chronic MENINGITIS, and other conditions. (From Adams et al., Principles of Neurology, 6th ed, pp631-3) | 0 | 1.97 | 1 | 0 |
Experimental Leukemia [description not available] | 0 | 1.96 | 1 | 0 |
Ectopic ACTH Syndrome [description not available] | 0 | 1.97 | 1 | 0 |
Ectopic Hormone Syndromes [description not available] | 0 | 1.97 | 1 | 0 |
ACTH Syndrome, Ectopic Symptom complex due to ACTH production by non-pituitary neoplasms. | 0 | 1.97 | 1 | 0 |
Nutritional Disorders [description not available] | 0 | 1.96 | 1 | 0 |
Nutrition Disorders Disorders caused by nutritional imbalance, either overnutrition or undernutrition. | 0 | 1.96 | 1 | 0 |
Reticulum Cell-Like Sarcoma, Yoshida [description not available] | 0 | 1.95 | 1 | 0 |
Petechiae Pinhead size (3 mm) skin discolorization due to hemorrhage. | 0 | 1.94 | 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 | 1.94 | 1 | 0 |
Anemia, Hemolytic, Acquired [description not available] | 0 | 1.94 | 1 | 0 |
Leucocythaemia [description not available] | 0 | 1.94 | 1 | 0 |
Erythremia [description not available] | 0 | 1.94 | 1 | 0 |
Anemia, Hemolytic A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES). | 0 | 1.94 | 1 | 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 | 1.94 | 1 | 0 |
Polycythemia Vera A myeloproliferative disorder of unknown etiology, characterized by abnormal proliferation of all hematopoietic bone marrow elements and an absolute increase in red cell mass and total blood volume, associated frequently with splenomegaly, leukocytosis, and thrombocythemia. Hematopoiesis is also reactive in extramedullary sites (liver and spleen). In time myelofibrosis occurs. | 0 | 1.94 | 1 | 0 |