| Description | Gene-phenotype associations extracted from published GWAS by automated text-mining |
| Measurement | genetic association by text-mining |
| Association | gene-phenotype associations by automated GWAS curation |
| Category | disease or phenotype associations |
| Resource | HuGE Navigator |
| Citation(s) | |
| Last Updated | 2015 Apr 06 |
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Attribute Similarity
Gene Attribute
Gene Similarity
2752 sets of genes associated with phenotypes by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
| Gene Set | Description |
|---|---|
| Psychopathology | |
| Hemorrhagic Septicemia | |
| Meniere's Disease | A vestibular disease characterized by vertigo, low-pitched tinnitus and hearing loss. |
| Echogenic Bowel | Echogenic bowel is defined as fetal bowel with homogenous areas of echogenicity that are equal to or greater than that of surrounding bone. |
| Immune Reconstitution Inflammatory Syndrome | |
| 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. |
| Jaundice | Yellow pigmentation of the skin or sclera due to bilirubin, which in turn is the result of increased bilirubin concentration in the bloodstream. |
| Cystadenocarcinoma, Mucinous | |
| Brain Injury, Chronic | |
| Schizophrenia, Catatonic | |
| Cholecystitis, Acute | |
| Thrombophilia | OMIM mapping confirmed by DO. [LS]. |
| Hereditary Sensory and Motor Neuropathy | |
| Efficiency | |
| Community-Acquired Infections | |
| Pick Disease of the Brain | |
| Hemoglobin SC Disease | OMIM mapping confirmed by DO. [LS]. |
| Choanal Atresia | OMIM mapping confirmed by DO. [SN]. |
| Drowning | |
| Dyspepsia | |
| Chordoma | A notochordal cancer that derives_from cellular remnants of the notochord. |
| Mitral Valve Prolapse | A mitral valve disease where one or both of the cusps of the mitral valve bulge or collapse backward in the left atrium during systole. |
| Ovarian Cysts | the appearance of fluid-filled sacs within the ovary |
| Psychiatric Status Rating Scales | |
| Carotid Stenosis | |
| Progeria | OMIM mapping confirmed by DO. [SN]. |
| Periapical Granuloma | |
| Anoxia | absence or almost complete absence of oxygen from inspired gases, in blood or tissues |
| Common Variable Immunodeficiency | A hypogammaglobulinemia that is results in insufficient production of antibodies needed to respond to exposure of pathogens and is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells. Patients with common variable immunodeficiency have marked reduction in serum levels of both immunoglobulin G (IgG) and immunoglobulin A (IgA); about half of these patients also have reduced immunoglobulin M (IgM). |
| Neuralgia | |
| Epilepsy, Generalized | |
| Duodenal Neoplasms | |
| Aneurysm, Ruptured | |
| Neoplasms, Squamous Cell | |
| Heart Septal Defects, Ventricular | |
| Paired-Associate Learning | |
| Lymphohistiocytosis, Hemophagocytic | |
| Agoraphobia | A phobic disorder involving the specific anxiety about being in a place or situation where escape is difficult or embarrassing or where help may be unavailable. |
| AIDS-Related Opportunistic Infections | |
| Anemia, Iron-Deficiency | |
| Stomach Diseases | |
| Neoplasms, Second Primary | |
| Adrenal Cortex Neoplasms | |
| Congenital Hypothyroidism | A hypothyroidism that is present at birth. |
| Diabetic Ketoacidosis | OMIM mapping confirmed by DO. [SN]. |
| Sturge-Weber Syndrome | Sturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder characterized by facial capillary malformations and/or cerebral and ocular ipsilateral vascular malformations that result in variable degrees of ocular and neurological anomalies. |
| Cocarcinogenesis | |
| Abortion, Missed | |
| Heart Block | Impaired conduction of cardiac impulse occurring anywhere along the conduction pathway. |
| Sex Chromosome Disorders of Sex Development | |
| Congenital Hyperinsulinism | |
| Hyperpigmentation | excess of pigment in any or all tissues or a part of a tissue |
| Hernia, Hiatal | |
| 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.|A usually exophytic mass attached to the underlying tissue by a broad base or a thin stalk. Polyps can be neoplastic or non-neoplastic. Neoplastic polyps usually represent proliferations of the epithelium, and are commonly seen in the gastrointestinal tract. Polyps of the gastrointestinal tract are often called adenomas, are associated with dysplasia, and may eventually transform into carcinomas. Non-neoplastic polyps may be inflammatory, degenerative, or the result of malformations. -- 2004|A usually exophytic mass attached to the underlying tissue by a broad base or a thin stalk. Polyps can be neoplastic or non-neoplastic. Neoplastic polyps usually represent proliferations of the epithelium, and are commonly seen in the gastrointestinal tract. Polyps of the gastrointestinal tract are often called adenomas, are associated with dysplasia, and may eventually transform into carcinomas. Non-neoplastic polyps may be inflammatory, degenerative, or the result of malformations. |
| Multiple Trauma | |
| Meningitis | Meningitis is a nervous system infectious disease characterized as an inflammation of the pia-arachnoid meninges. It can be caused by growth of bacteria, fungi, or parasites within the subarachnoid space or by the growth of bacteria or viruses within the meningeal or ependymal cells. Meningitis is a diffuse infection caused by a variety of different agents. |
| Vasculitis | A vascular disease that is characterized by inflammation of the blood vessels. |
| Tuberculosis, Pleural | |
| Child Development Disorders, Pervasive | |
| Helminthiasis | A parasitic infectious disease that occurs when part of the body is infested with parasitic worms such as cestodes, nematodes and trematodes. |
| Arrhythmia | Any cardiac rhythm other than the normal sinus rhythm. Such a rhythm may be either of sinus or ectopic origin and either regular or irregular. An arrhythmia may be due to a disturbance in impulse formation or conduction or both. |
| Macular Degeneration | A retinal degeneration characterized by gradual deterioration of light-sensing cells in the tissues at the back of the eye; symptoms include vision loss. |
| Neuromyelitis Optica | A central nervous system disease characterized by acute neuritis located_in eye and demyelination located_in optic nerve and located_in spinal cord. |
| Pulmonary Embolism | An artery disease characterized by a blockage of the main artery of the lung or one of its branches by a substance that has travelled from elsewhere in the body, e.g. a blood clot. |
| Hypertension, Pulmonary | |
| Bronchopneumonia | A pneumonia involving inflammation of lungs that begins in the terminal bronchioles, which become clogged with thick mucus that forms consolidated patches in adjacent lobules. It is caused by bacteria and viruses. |
| Carotid Artery Diseases | |
| Brain Death | |
| Meconium Aspiration Syndrome | |
| Lentigo | |
| Wet Macular Degeneration | A form of RETINAL DEGENERATION in which abnormal CHOROIDAL NEOVASCULARIZATION occurs under the RETINA and MACULA LUTEA, causing bleeding and leaking of fluid. This leads to bulging and or lifting of the macula and the distortion or destruction of central vision. |
| Mixed Connective Tissue Disease | A collagen disease that is considered an overlap of three diseases, systemic lupus erythematosus, scleroderma, and polymyositis with very high titers of circulating antinuclear antibody to a ribonucleoprotein antigen. |
| Opioid-Related Disorders | |
| Intestinal Neoplasms | |
| Hypertension, Portal | |
| Bronchitis | A bronchial disease that is an inflammation of the bronchial tubes. It is caused by bacteria and viruses. The disease has_symptom cough with mucus, has_symptom shortness of breath, has_symptom low fever and has_symptom chest tightness. |
| Neuromuscular Diseases | |
| Blood Loss, Surgical | |
| Anemia, Refractory, with Excess of Blasts | |
| Myocardial Stunning | |
| Anemia, Aplastic | |
| Extinction, Psychological | |
| Sarcoma, Kaposi | |
| Bile Duct Neoplasms | |
| Congenital Abnormalities | |
| Thrombocytopenia | A blood platelet disease characterized by low a platelet count in the blood. |
| Hyperlipidemia, Familial Combined | |
| Hemorrhagic Disorders | |
| Lymphopenia | A leukopenia that is the condition of having an abnormally low level of lymphocytes in the blood. |
| Anodontia | |
| Neoplasms, Glandular and Epithelial | |
| Cholera | A primary bacterial infectious disease that is described as an acute, diarrheal illness caused by infection of the intestine with the bacterium Vibrio cholerae, which is characterized by profuse watery diarrhea, vomiting, leg cramps, circulatory collapse and shock. |
| Heart Injuries | |
| Prosthesis-Related Infections | |
| Cadaver | |
| Choriocarcinoma | An aggressive malignant tumor arising from trophoblastic cells. The vast majority of cases arise in the uterus and represent gestational choriocarcinomas that derive from placental trophoblastic cells. Approximately half of the cases develop from a complete hydatidiform mole. A minority of cases arise in the testis or the ovaries. There is often marked elevation of human chorionic gonadotropin (hCG) in the blood. Choriocarcinomas disseminate rapidly through the hematogenous route; the lungs are most frequently affected. |
| Liver Cirrhosis | |
| Proctitis | Proctitis is an inflammation of the rectum. |
| Endotoxemia | |
| Respiratory Sounds | |
| West Nile Fever | A viral infectious disease that results_in infection, has_material_basis_in West Nile virus, which is transmitted_by Culex and transmitted_by Aedes mosquitoes. The infection has_symptom fever, has_symptom sore throat, has_symptom headache, has_symptom body ache, has_symptom nausea, has_symptom maculopapular rash and has_symptom vomiting. |
| Neoplasms, Radiation-Induced | |
| Anemia, Hemolytic, Congenital Nonspherocytic | |
| Cerebral Hemorrhage, Traumatic | |
| Tibial Fractures | |
| Polycystic Kidney, Autosomal Dominant | |
| Burnout, Professional | |
| Food Hypersensitivity | A hypersensitivity reaction type I disease that is an abnormal response to a food, triggered by the body's immune system. |
| beta-Thalassemia | A thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin. |
| Central Serous Chorioretinopathy | |
| Mydriasis | Abnormal dilatation of the iris. |
| Hyperbilirubinemia, Hereditary | |
| Dermoid Cyst | |
| Central Nervous System Vascular Malformations | |
| Cardiomyopathy, Restrictive | |
| Protein Deficiency | |
| Nijmegen Breakage Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Nephrosis, Lipoid | |
| Basal Cell Nevus Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Nut Hypersensitivity | |
| Arcus Senilis | OMIM mapping confirmed by DO. [SN]. |
| Hemangiosarcoma | A malignant tumor arising from the endothelial cells of the blood vessels. Microscopically, it is characterized by frequently open vascular anastomosing and branching channels. The malignant cells that line the vascular channels are spindle or epithelioid and often display hyperchromatic nuclei. Angiosarcomas most frequently occur in the skin and breast. Patients with long-standing lymphedema are at increased risk of developing angiosarcoma. |
| Adenoma, Liver Cell | |
| Thromboembolism | The formation of a blood clot inside a blood vessel that subsequently travels through the blood stream from the site where it formed to another location in the body, generally leading to vascular occlusion at the distant site. |
| Multiple Organ Failure | |
| Hirschsprung Disease | A megacolon that is characterized by a blockage of the large intestine due to improper muscle movement in the bowel. |
| Dyskinesia, Drug-Induced | |
| Shy-Drager Syndrome | OMIM mapping confirmed by DO. [LS]. |
| Neonatal Abstinence Syndrome | A withdrawal disorder that is characterized by a group of problems that occur in a newborn who was exposed to addictive illegal or prescription drugs while in the mother's womb or postnatally following the discontinuance of drug treatment. |
| Attention | |
| Adenocarcinoma, Mucinous | |
| Thermosensing | |
| Brain Concussion | |
| Virus Diseases | |
| Language Disorders | |
| DNA Damage | |
| Menstruation Disturbances | |
| Optic Neuritis | An optic nerve disease that results_in inflammation located_in optic nerve which may cause a complete or partial loss of vision. |
| Maxillary Diseases | |
| Roseolovirus Infections | |
| Osteogenesis Imperfecta | An osteochondrodysplasia that has_material_basis_in a deficiency in type-I collagen which results_in brittle bones and defective connective tissue. |
| Hereditary Motor and Sensory Neuropathies | |
| Retinal Detachment | OMIM mapping confirmed by DO. [SN]. |
| Arthropathy, Neurogenic | |
| Monoclonal Gammopathy of Undetermined Significance | |
| Gonorrhea | A primary bacterial infectious disease that is a sexually transmitted infection, located_in uterus, located_in fallopian tube, located_in urethra, located_in mouth, located_in throat, located_in eye or located_in anus, has_material_basis_in Neisseria gonorrhoeae, which is transmitted_by contact with the penis, vagina, mouth, or anus or transmitted_by congenitally from mother to baby during delivery. The infection has_symptom burning sensation during urination, has_symptom discharge from the penis, has_symptom increased vaginal discharge, or has_symptom vaginal bleeding between periods. |
| Pharyngeal Neoplasms | |
| Encephalitis | Encephalitis is a nervous system infectious disease characterized as an acute inflammation of the brain. The usual cause is a viral infection, but bacteria can also cause it. Cases can range from mild to severe. For mild cases, you could have flu-like symptoms. Serious cases can cause severe headache, sudden fever, drowsiness, vomiting, confusion and seizures. |
| Metabolism, Inborn Errors | |
| Bronchial Spasm | |
| Esophageal Achalasia | An esophageal disease that is characterized by an inability of the esophagus to move food toward the stomach resulting from the lower esophogeal sphincter not fully relaxing during swallowing. |
| Motor Skills | |
| Hepatitis D, Chronic | |
| Brugada Syndrome | A heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death. |
| Pattern Recognition, Physiological | |
| Mercury Poisoning, Nervous System | |
| Multiple Sclerosis, Chronic Progressive | |
| Aspergillosis, Allergic Bronchopulmonary | |
| Choroiditis | |
| Set | SET nuclear proto-oncogene|The protein encoded by this gene inhibits acetylation of nucleosomes, especially histone H4, by histone acetylases (HAT). This inhibition is most likely accomplished by masking histone lysines from being acetylated, and the consequence is to silence HAT-dependent transcription. The encoded protein is part of a complex localized to the endoplasmic reticulum but is found in the nucleus and inhibits apoptosis following attack by cytotoxic T lymphocytes. This protein can also enhance DNA replication of the adenovirus genome. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] |
| Rheumatic Diseases | |
| Keratoderma, Palmoplantar | |
| DiGeorge Syndrome | A T cell deficiency disease that is the result of a large deletion of chromosome 22 which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production. |
| Cholesterol Ester Storage Disease | |
| Stress Disorders, Traumatic, Acute | |
| Amnesia | A cognitive disorder where the memory is disturbed or lost and involves the loss of memories previously established, loss of the ability to create new memories, or loss of the ability to learn new information. |
| Lymphoma, Large-Cell, Ki-1 | |
| Mastocytosis, Systemic | |
| Syncope | Syncope refers to a generalized weakness of muscles with loss of postural tone, inability to stand upright, and loss of consciousness. Once the patient is in a horizontal position, blood flow to the brain is no longer hindered by gravitation and consciousness is regained. Unconsciousness usually lasts for seconds to minutes. Headache and drowsiness (which usually follow seizures) do not follow a syncopal attack. Syncope results from a sudden impairment of brain metabolism usually due to a reduction in cerebral blood flow. |
| Salivary Gland Neoplasms | |
| Paralyses, Familial Periodic | |
| Muscle Hypotonia | Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching. |
| Pharyngitis | An upper respiratory tract disease involving inflammation of the throat or pharynx resulting from bacterial, viral, fungal infections or irritants like pollutants or chemical substances and smoking. The infection is often referred to as sore throat. The symptoms include pain during swallowing, enlarged tonsils coated with a white discharge, runny nose, cough and slight fever. |
| Cleft Lip | |
| Vomiting | Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic contractions. |
| Anthropology | |
| Superinfection | |
| Coronary Thrombosis | |
| Precancerous Conditions | |
| Burns | |
| Laryngeal Neoplasms | |
| Prognathism | Abnormal prominence of the chin related to increased length of the mandible. |
| Child Behavior Disorders | |
| Hematologic Neoplasms | |
| MELAS Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Atrial Fibrillation | A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain. |
| Thrombosis | formation within a tissue or the vascular lumen of a thrombus, an aggregation of coagulated blood containing platelets, fibrin, and entrapped cellular elements |
| Cytomegalovirus Infections | A Herpesviridae infectious disease that results_in infection in animals and humans, has_agent Cytomegalovirus, which is transmitted_by contact with the infected person's bodily fluids or transmitted_by sexual contact, or transmitted_by blood transfusions.|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. |
| Venous Thrombosis | Formation of a blood clot (thrombus) inside a vein, causing the obstruction of blood flow. |
| Hypokalemia | |
| Leprosy | A chronic granulomatous infection caused by MYCOBACTERIUM LEPRAE. The granulomatous lesions are manifested in the skin, the mucous membranes, and the peripheral nerves. Two polar or principal types are lepromatous and tuberculoid. |
| Fissure in Ano | |
| Mycobacterium Infections | |
| Vulvodynia | |
| Salmonella Infections | |
| Pain Perception | |
| Neoplasm Recurrence, Local | |
| Cafe-au-Lait Spots | Cafe-au-lait spots are hyperpigmented lesions that can vary in color from light brown to dark brown with smooth borders and having a size of 1.5 cm or more in adults and 0.5 cm or more in children. |
| Amyloid Neuropathies | |
| Mesenteric Vascular Occlusion | |
| Parakeratosis | Abnormal formation of the keratinocytes of the epidermis characterized by persistence of nuclei, incomplete formation of keratin, and moistness and swelling of the keratinocytes. |
| Erythema Multiforme | A skin disease that is a type of allergic reaction located_in skin, which occurs in response to medications, infections, or illness. |
| Thymoma | A thymus cancer that derives_from epithelial cells located_in the thymus. The tumor cells in a thymoma look similar to the normal cells of the thymus, grow slowly, and rarely spread beyond the thymus. |
| Scleroderma, Limited | |
| Tuberculosis, Miliary | |
| Leukemia, Hairy Cell | |
| Paraparesis, Tropical Spastic | |
| Wakefulness | |
| Silver-Russell Syndrome | OMIM mapping confirmed by DO. [LS]. |
| Movement Disorders | |
| Hyperlipoproteinemias | |
| Laron Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Demyelinating Autoimmune Diseases, CNS | |
| Ebstein Anomaly | A tricuspid valve disease that is a congenital heart defect in which the septal leaflet of the tricuspid valve is displaced towards the apex of the right ventricle of the heart. |
| Tobacco Use Disorder | |
| Gingival Pocket | |
| Angiomyolipoma | A cell type benign neoplasm that from perivascular epithelioid cells. |
| Hearing Loss | reduced ability to perceive auditory stimuli |
| Pregnancy Complications, Infectious | |
| Carcinoma | A type of malignant cancer that arises from epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. |
| Rh Isoimmunization | |
| Gaucher Disease | A sphingolipidosis characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body, especially within the bone marrow, spleen and liver. |
| Hyperinsulinism | |
| Epilepsy, Frontal Lobe | |
| Chromosome Fragility | |
| Concept Formation | |
| Budd-Chiari Syndrome | |
| Angina Pectoris | Paroxysmal chest pain that occurs with exertion or stress and is related to myocardial ischemia. |
| Candidemia | |
| Cardiomyopathy, Hypertrophic, Familial | |
| Eye Hemorrhage | bleeding into the eye |
| Absenteeism | |
| Tangier Disease | OMIM mapping confirmed by DO. [LS]. |
| Habituation, Psychophysiologic | |
| Angioneurotic Edema | condition similar to urticarai but with swelling occuring in a lower layer of the dermis as well as in the subcutis |
| Language Development Disorders | |
| Pseudohypoaldosteronism | |
| Hemorrhage | loss of blood from the vascular compartment to the exterior or into nonvascular body space as a result of rupture or severance of the blood vessels |
| Lichenoid Eruptions | |
| Erythema Chronicum Migrans | |
| Hutchinson's Melanotic Freckle | |
| Wegener Granulomatosis | An autoimmune disease that is a vasculitis that is located_in lung, located_in kidney, located_in skin resulting from an autoimmune attack by antineutrophil cytoplasmic antibodies against small and medium-size blood vessels. |
| Coffin-Lowry Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Hypertrophy, Left Ventricular | |
| Carcinoma, Small Cell | |
| Airway Obstruction | |
| Hypersensitivity | An immune system disease that is an exaggerated immune response to allergens, such as insect venom, dust mites, pollen, pet dander, drugs or some foods. |
| Hirsutism | Abnormally increased hair growth referring to a male pattern of body hair (androgenic hair). |
| Pulmonary Disease, Chronic Obstructive | |
| Schizophrenic Psychology | |
| Acanthosis Nigricans | OMIM mapping confirmed by DO. [SN]. |
| Hearing Loss, Central | |
| Persistent Hyperinsulinemia Hypoglycemia of Infancy | A carbohydrate metabolic disorder that involves low blood glucose resulting from an excess of insulin. |
| Fever of Unknown Origin | Fever in which the etiology cannot be ascertained. |
| DNA Degradation, Necrotic | |
| Implant Capsular Contracture | |
| 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. |
| Vulvar Vestibulitis | |
| Psychotherapy | |
| Judgment | |
| Postthrombotic Syndrome | A venous insufficiency that is characterized by aching pain, heaviness, swelling, cramps, itching, or tingling in the affected limb and is a chronic complication of deep venous thrombosis. |
| Chronobiology Disorders | |
| Psychomotor Performance | The coordination of a sensory or ideational (cognitive) process and a motor activity. |
| Necrosis | |
| Implosive Therapy | |
| Vasculitis, Leukocytoclastic, Cutaneous | |
| Abdomen, Acute | |
| Avitaminosis | A disorder that is caused by the deficiency of a vitamin. The deficiency may result from either suboptimal vitamin intake or conditions that prevent the vitamin's use or absorption in the body. Representative examples include beriberi caused by thiamine deficiency, scurvy caused by vitamin C deficiency, and rickets caused by vitamin D deficiency. |
| Chorioamnionitis | A placenta disease that is an inflammation of the fetal membranes (amnion and chorion) due to a bacterial infection. |
| Spinocerebellar Ataxias | |
| Latent Tuberculosis | |
| Skin Diseases | |
| Trachoma | A commensal bacterial infectious disease that results_in infection located_in eye, has_material_basis_in Chlamydia trachomatis (A, B, Ba and C serovars), which is transmitted_by contact with eye discharge from the infected person and transmitted_by congenital method. The infection causes eyelid to turn inward which makes eyelashes to scratch the cornea. |
| Rhabdomyolysis | Necrosis or disintegration of skeletal muscle often followed by myoglobinuria. |
| Dermatitis, Allergic Contact | |
| Trismus | Limitation in the ability to open the mouth. |
| Olfaction Disorders | |
| Dyslexia | |
| Pruritus | Pruritus is an itch or a sensation that makes a person want to scratch. This term refers to an abnormally increased disposition to experience pruritus. |
| Pneumonia, Bacterial | |
| Autistic Disorder | An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years. |
| Emphysema | A subcategory of chronic obstructive pulmonary disease (COPD). It occurs in people who smoke and suffer from chronic bronchitis. It is characterized by inflation of the alveoli, alveolar wall damage, and reduction in the number of alveoli, resulting in difficulty breathing. |
| Acute-Phase Reaction | |
| Hyperthyroxinemia | |
| Empyema, Pleural | A soft tissue infectious disease that involves accumulation of pus in the pleural cavity as a result of infection within the lung (pneumonia) or a lung abscess spreading into the space. The symptoms include cough, fever, chest pain, sweating and shortness of breath. |
| Alcoholic Neuropathy | |
| Child Nutrition Disorders | |
| Multiple Endocrine Neoplasia Type 2b | An autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities. |
| Multiple Endocrine Neoplasia Type 2a | An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis. |
| Dupuytren's Contracture | |
| 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) |
| Hyperalgesia | increased sensitivity to painful stimuli; can be due to inflammatory response or due to damage to soft tissue containing nociceptors or injury to a peripheral nerve; it can be primary (at the site of the injury) or secondary (in the surrounding undamaged area) |
| Sleep Disorders, Circadian Rhythm | |
| Soft Tissue Neoplasms | |
| Rhinitis, Allergic, Perennial | |
| Eclampsia | A pre-eclampsia characterized by the presence of seizures. |
| Hyperprolactinemia | An acquired metabolic disease that has_material_basis_in the presence of abnormally-high levels of prolactin in the blood. |
| Nausea | A sensation of unease in the stomach together with an urge to vomit. |
| Hartnup Disease | An amino acid metabolic disorder that iis caused by abnormalities of the renal tubules and is characterized especially by aminoaciduria involving only monocarboxylic monoamines, a dry red scaly rash, and episodic muscular incoordination due to the effects of the disease on the cerebellum. |
| Bronchitis, Chronic | |
| Dementia, Multi-Infarct | |
| Echinococcosis | A parasitic helminthiasis infectious disease that involves parasitic infection of humans and domestic animals caused by the larval stages of tapeworms of the genus Echinococcus in the liver, lungs, spleen, brain, heart and kidneys. |
| Infectious Mononucleosis | A viral infectious disease that results_in inflammation, located_in pharynx, has_material_basis_in Human herpesvirus 4 and has_symptom fever, has_symptom fatigue, has_symptom lymphadenopathy, and has_symptom splenomegaly. |
| Splenomegaly | Abnormal increased size of the spleen. |
| Aneurysm | Abnormal outpouching or sac-like dilatation in the wall of an atery, vein or the heart. |
| Antithrombin III Deficiency | An inherited blood coagulation disease characterized by the tendency to form clots in the veins. |
| Vitamin K Deficiency | |
| Adjustment Disorders | |
| Autoimmune Lymphoproliferative Syndrome | A hypersensitivity reaction type IV disease that is an inherited disorder in which the body cannot properly regulate the number of immune system cells (lymphocytes). It is characterized by the production of an abnormally large number of lymphocytes. Accumulation of excess lymphocytes results in enlargement of the lymph nodes, the liver, and the spleen. |
| HIV-Associated Lipodystrophy Syndrome | |
| Vision | |
| Precursor T-Cell Lymphoblastic Leukemia-Lymphoma | |
| Synovitis | A connective tissue disease that results_in inflammation located_in synovial membrane that lines a synovial joint which causes pain and swelling. |
| Deficiency Diseases | |
| Cerebral Infarction | |
| Oculocerebrorenal Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Scleroderma, Localized | |
| Suppuration | |
| Reactive Attachment Disorder | |
| Ulcer | |
| Elliptocytosis, Hereditary | |
| Dyspnea | Difficult or labored breathing. |
| Spondylitis | |
| Craniosynostoses | |
| Hemangioblastoma | |
| Time and Motion Studies | |
| Skin Abnormalities | |
| Back Pain | An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the back. |
| Carcinoma, Giant Cell | |
| Herpesviridae Infections | |
| Creutzfeldt-Jakob Syndrome | |
| Tachycardia | A rapid heartrate that exceeds the range of the normal resting heartrate for age. |
| Neovascularization, Pathologic | |
| Peroneal Neuropathies | |
| Priapism | A peripheral vascular disease characterized by blood trapped in the penis that is unable to drain. |
| Failure to Thrive | Failure to thrive (FTT) refers to a child whose physical growth is substantially below the norm. |
| Neuroaxonal Dystrophies | |
| Intracranial Hypertension | |
| Bardet-Biedl Syndrome | An autosomal recessive disease that results from mutations in multiple BBS genes affecting cellular cilia structure or function (ciliopathy) resulting in variable presentation and characterized principally by obesity, retinitis pigmentosa,vision loss, polydactyly, mental retardation, hypogonadism, and renal failure in some cases. |
| Fetal Macrosomia | The term large for gestational age applies to babies whose birth weight lies above the 90th percentile for that gestational age. |
| Mucocutaneous Lymph Node Syndrome | A lymphadenitis characterized by swelling of cervical lymph nodes in infants and young children and inflammation of medium-sized blood vessels located_in body, has_symptom fever, has_symptom congestion of ocular conjunctivae, has_symptom reddening of lips, has_symptom reddening of oral cavity, has_symptom protuberance of tongue papillae and has_symptom edema of extremities. |
| Aneuploidy | chromosome count is not an exact multiple of the haploid number |
| Osteoarthritis, Knee | |
| Ascariasis | A parasitic helminthiasis infectious disease that involves infection of the intestine with the nematode Ascaris lumbricoides. Larvae migrating through the lungs cause cough, wheezing and hemoptysis. Bowel or biliary obstruction causes cramping abdominal pain, nausea, and vomiting. Peritonitis, enlargement of the liver or spleen, toxicity and pneumonia are observed when larvae get into the portal circulation. |
| Tremor | An unintentional, oscillating to-and-fro muscle movement. |
| Ovarian Neoplasms | |
| Facial Neoplasms | |
| Schizophrenia, Paranoid | |
| Discrete Subaortic Stenosis | |
| Leukemia, Mast-Cell | |
| Conditioning, Classical | |
| Crigler-Najjar Syndrome | A bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT). |
| Mood Disorders | |
| Tinea Versicolor | |
| Alcohol-Related Disorders | |
| Nocturia | Abnormally increased production of urine during the night leading to an unusually frequent need to urinate. |
| Muscular Dystrophies, Limb-Girdle | |
| Infertility, Female | |
| Lipid Metabolism, Inborn Errors | |
| Mental Processes | Conceptual functions or thinking in all its forms. |
| Stomach Ulcer | |
| Hypoplastic Left Heart Syndrome | A congenital heart disease characterized by abnormal development of the left-sided structures of the heart. |
| Albuminuria | The presence of albumin in the urine, an indicator of KIDNEY DISEASES. |
| Alcohol-Induced Disorders, Nervous System | |
| Sigmoid Neoplasms | |
| Abruptio Placentae | A placenta disease that is characterized by separation of the placental lining from the uterus of the mother. |
| Fibromatosis, Aggressive | |
| Diabetic Cardiomyopathies | |
| Hypercholesterolemia | An increased concentration of cholesterol in the blood. |
| Leukemia-Lymphoma, Adult T-Cell | |
| Paraproteinemias | |
| Giant Cell Tumor of Bone | A bone tumor composed of cellular spindle-cell stroma containing scattered multinucleated giant cells resembling osteoclasts. |
| Paratyphoid Fever | A primary bacterial infectious disease that results_in infection located_in intestine, has_material_basis_in Salmonella enterica subsp enterica serovar Paratyphi A, B or C, which are transmitted_by ingestion of contaminated food. The infection has_symptom fever, has_symptom headache, has_symptom abdominal pain, has_symptom malaise, has_symptom anorexia, has_symptom constipation, has_symptom rosy spots on the central body, has_symptom non productive cough (in early stage of illness), has_symptom bradycardia, and has_symptom hepatosplenomegaly. |
| Pseudotumor Cerebri | OMIM mapping confirmed by DO. [SN]. |
| Adrenocortical Carcinoma | An adrenal cortex cancer that forms in the outer layer of tissue of the adrenal gland and that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. |
| Cholecystolithiasis | |
| Papilloma, Inverted | |
| 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).|The presence of an increased amount of blood in a part or organ; engorgement. |
| Reflex | An automatic response to a stimulus beginning with a nerve impulse from a receptor and ending with the action of an effector such as a gland or a muscle. Signaling never reaches a level of consciousness. |
| Alcoholism | |
| Retinal Artery Occlusion | |
| Tricuspid Valve Insufficiency | A tricuspid valve disease that is characterized by failure of the heart's tricuspid valve to close properly during systole. As a result, with each heart beat, blood is pumped out from the right side of the heart in the opposite direction to normal. |
| Embolism, Paradoxical | |
| Addison Disease | An adrenal cortical hypofunction that is characterized by insufficient steroid hormone production by the adrenal glands. |
| Bronchiolitis | A lung disease that is an inflammation of the bronchioles, the smallest air passages of the lungs. It is caused by viruses and bacteria. The disease has_symptom cough, has_symptom wheezing, has_symptom shortness of breath, has_symptom fever, has_symptom nasal flaring in infants and has_symptom bluish skin due to lack of oxygen. |
| Latex Hypersensitivity | |
| Cough | A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation. |
| Cognition Disorders | |
| Trichotillomania | An impulse control disorder that involves the uncontrollable plucking of ones hair. |
| Sneddon Syndrome | |
| Quadriplegia | |
| Parvoviridae Infections | |
| Sclerosis | |
| Albinism | An abnormal reduction in the amount of pigmentation (reduced or absent) of skin, hair and eye (iris and retina). |
| Neurofibromatosis 1 | |
| Neurofibromatosis 2 | |
| Chest Pain | An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the chest. |
| Barrett Esophagus | Metaplasia of the lower esophagus that is characterized by replacement of squamous epithelium with columnar epithelium, occurs especially as a result of chronic gastroesophageal reflux, and is associated with an increased risk for esophageal carcinoma. |
| Vaginosis, Bacterial | |
| alpha 1-Antitrypsin Deficiency | A plasma protein metabolism disease that has_material_basis_in defective production of the protease inhibitor alpha 1-antitrypsin (A1AT), leading to decreased A1AT activity in the blood and lungs, and deposition of excessive abnormal A1AT protein in liver cells. |
| Choledocholithiasis | |
| Myotonic Disorders | |
| Lupus Erythematosus, Discoid | |
| Hypersensitivity, Immediate | |
| Laryngeal Diseases | |
| Hemostatic Disorders | |
| 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. |
| Muscle Weakness | Reduced strength of muscles. |
| Hyperglycemia | |
| Fatty Liver | The presence of steatosis in the liver. |
| Intracranial Hemorrhages | |
| Heart Failure, Congestive | |
| Thrombophlebitis | A phlebitis that results from a blood clot in the vessel. |
| Illusions | |
| Pityriasis Rosea | |
| Osteoarthritis, Hip | |
| Yang Deficiency | |
| Pre-Eclampsia | A hypertension occurring during pregnancy characterized by large amounts of protein in the urine (proteinuria) and edema, usually by the last trimester of pregnancy. |
| Metabolic Syndrome X | OMIM mapping confirmed by DO. [SN]. |
| Data Display | |
| Bacteremia | An infection that has as part bacteria located in the blood. |
| Lung Diseases, Interstitial | |
| Prader-Willi Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Endocarditis | A heart disease involving non-infectious inflammation of the endocardium (inner layer of the heart).|Inflammation of the inner lining of the heart (ENDOCARDIUM), the continuous membrane lining the four chambers and HEART VALVES. It is often caused by microorganisms including bacteria, viruses, fungi, and rickettsiae. Left untreated, endocarditis can damage heart valves and become life-threatening.|Inflammation of the endocardium. |
| Wound Infection | |
| Coronary Artery Disease | Thickening and loss of elasticity of the CORONARY ARTERIES, leading to progressive arterial insufficiency (CORONARY DISEASE).|Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause.|Narrowing of the coronary arteries due to fatty deposits inside the arterial walls.|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. |
| Hyperparathyroidism, Secondary | |
| Perception | |
| Hyperuricemia | An acquired metabolic disease that has_material_basis_in an abnormally high level of uric acid in the blood. |
| Brief Psychiatric Rating Scale | |
| Fatty Liver, Alcoholic | |
| Machado-Joseph Disease | A spinocerebellar ataxia that is characterized by slow degeneration of the hindbrain and has_material_basis_in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene. |
| Infection | The state of being infected such as from the introduction of a foreign agent such as serum, vaccine, antigenic substance or organism. |
| Gait Ataxia | A type of ataxia characterized by the impairment of the ability to coordinate the movements required for normal walking. Gait ataxia is characteirzed by a wide-based staggering gait with a tendency to fall. |
| Vestibular Diseases | |
| Wounds, Penetrating | |
| Pemphigoid, Bullous | |
| Overbite | Maxillary teeth cover the mandibular teeth when biting to an increased degree. |
| Scleroderma, Systemic | |
| Peptic Ulcer Hemorrhage | |
| Hand, Foot and Mouth Disease | A viral infectious disease that results_in infection located_in skin, has_material_basis_in Human coxsackievirus A16 or has_material_basis_in Human enterovirus 71, which are transmitted_by contaminated fomites, and transmitted_by contact with nose and throat secretions, saliva, blister fluid and stool of infected persons. The infection has_symptom fever, has_symptom poor appetite, has_symptom malaise, has_symptom sore throat, has_symptom painful sores in the mouth, and has_symptom skin rash on the palms of the hands and soles of the feet. |
| Corneal Ulcer | |
| LEOPARD Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Kidney Diseases | |
| Mandibular Diseases | |
| Odontogenic Tumors | |
| Gingival Hyperplasia | |
| Hydrophthalmos | |
| 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)|A neurodegenerative disease that results_from degeneration of the central nervous system that often impairs the sufferer's motor skills, speech, and other functions. |
| Papillon-Lefevre Disease | OMIM mapping confirmed by DO. [SN]. |
| Neoplasms, Cystic, Mucinous, and Serous | |
| Directive Counseling | |
| IgA Deficiency | A B cell deficiency that is an autosomal recessive disorder caused by mutation in the IgA (CD79 alpha) antigen receptor. |
| Schizophrenia | A major psychotic disorder characterized by abnormalities in the perception or expression of reality. It affects the cognitive and psychomotor functions. Common clinical signs and symptoms include delusions, hallucinations, disorganized thinking, and retreat from reality.|A severe emotional disorder of psychotic depth characteristically marked by a retreat from reality with delusion formation, HALLUCINATIONS, emotional disharmony, and regressive behavior. |
| Hypercalcemia | |
| Germinoma | A germ cell cancer that lacks histologic differentiation. It usually refers to a tumor in the brain. |
| Arousal | |
| Water-Electrolyte Imbalance | |
| Myoclonic Epilepsies, Progressive | |
| Epidermal Cyst | a benign mass derived from the epidermis or the epithelium of a hair follicle, formed by enclosure of epithelium within the dermis and filled with keratin and lipid-rich inclusions |
| Moyamoya Disease | A cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots. |
| Hypoxia, Brain | |
| Hypersomnolence, Idiopathic | |
| Gilbert Disease | |
| Hyperglycinemia, Nonketotic | |
| Pyoderma Gangrenosum | |
| Ventricular Premature Complexes | |
| Iron Metabolism Disorders | |
| Lichen Planus | A lichen disease that is located_in skin, located_in tongue or located_in oral mucosa, which presents itself in the form of papules, lesions or rashes. The cause is not known. |
| Myocardial Reperfusion Injury | |
| Foot Dermatoses | |
| Paraplegia | |
| Blastocystis Infections | |
| Spasms, Infantile | |
| Kaposi Varicelliform Eruption | |
| Pregnancy Complications, Hematologic | |
| Exophthalmos | An eye disease that is characterized by a bulging of the eye anteriorly out of the orbit. |
| Abortion, Spontaneous | |
| Genital Neoplasms, Male | |
| Proteus Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Hypophosphatasia | OMIM mapping confirmed by DO. [SN]. |
| Femoral Neck Fractures | |
| Iridocyclitis | |
| AIDS Dementia Complex | A HIV encephalopathy and is_a brain disease that results_in infection in adults located_in brain, has_agent Human immunodeficiency virus 1 or has_agent Human immunodeficiency virus 2. The infection has_symptom cognitive impairment, has_symptom motor dysfunction, has_symptom behavioral change, and has_symptom speech problems.|A brain disease and is_a HIV encephalopathy that results_in infection in adults located_in brain, has_agent Human immunodeficiency virus 1 or has_agent Human immunodeficiency virus 2. The infection has_symptom cognitive impairment, has_symptom motor dysfunction, has_symptom behavioral change, and has_symptom speech problems. |
| Olivopontocerebellar Atrophies | |
| Multiple Myeloma | A bone marrow-based plasma cell neoplasm characterized by a serum monoclonal protein and skeletal destruction with osteolytic lesions, pathological fractures, bone pain, hypercalcemia, and anemia. Clinical variants include non-secretory myeloma, smoldering myeloma, indolent myeloma, and plasma cell leukemia. (WHO, 2001)|A myeloma that is located_in the plasma cells in bone marrow.|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. |
| 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. |
| Muscular Disorders, Atrophic | |
| Appendiceal Neoplasms | |
| Heart Aneurysm | |
| 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).|A Herpesviridae infectious disease that results_in infection, has_agent Human herpesvirus 4, which is transmitted_by contact with the saliva. |
| Microsatellite Instability | |
| Tauopathies | |
| Leukoplakia, Oral | |
| Croup | A respiratory system infectious disease that involves inflammation, edema, and subsequent obstruction of the larynx, trachea, and bronchi. The disease is caused by viruses, bacteria, allergies and inhaled irritants. It is marked by episodes of difficult breathing and hoarse metallic cough in infants and young children. Croup is caused by parainfluenza virus (types 1 and 2), Influenza A and B viruses, Measles virus, adenovirus, respiratory syncytial virus, Staphylococcus and Streptococcus. |
| Pulmonary Aspergillosis | |
| 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) |
| Hyperbilirubinemia | An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism. |
| Tooth Abnormalities | |
| Infant, Newborn, Diseases | |
| Periodontal Diseases | |
| Lecithin Acyltransferase Deficiency | OMIM mapping confirmed by DO. [SN]. |
| Vitreoretinopathy, Proliferative | |
| Neurilemmoma | |
| Neurocysticercosis | A taeniasis that results from ingestion of eggs or larvae of the Taenia solium tapeworm in undercooked pork or fecally contaminated food or water, which subsequently infect the central nervous system, heart, muscles, subcutaneous tissues, and eyes. Neurocysticercosis causes seizures, mental disturbances, focal neurologic deficits and intracerebral lesions. |
| Behavior Control | |
| Aspergillosis | An opportunistic mycosis that involves a spectrum of diseases of humans and animals caused by members of the genus Aspergillus infecting lungs, brain, kidney,heart, bone, eyes, sinuses, skin and gastrointestinal tract. It is a serious illnesses in people with a weakened immune system. |
| Thyroiditis, Subacute | |
| Neoplasms, Basal Cell | |
| Hypophosphatemia | |
| Primary Myelofibrosis | A myeloma that is located_in the bone marrow which results_in bone marrow being replaced by fibrous (scar) tissue. |
| Leg Dermatoses | |
| Vitiligo | A disorder consisting of areas of macular depigmentation, commonly on extensor aspects of extremities, on the face or neck, and in skin folds. Age of onset is often in young adulthood and the condition tends to progress gradually with lesions enlarging and extending until a quiescent state is reached. |
| Simian Acquired Immunodeficiency Syndrome | |
| Philadelphia Chromosome | |
| Fractures, Ununited | |
| Cystitis, Interstitial | |
| Primary Ovarian Insufficiency | An ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40. |
| Williams Syndrome | |
| Gingival Hypertrophy | |
| Epidermolysis Bullosa Simplex | |
| Jaundice, Neonatal | |
| Pyelonephritis | |
| Dental Enamel Hypoplasia | |
| Stress, Psychological | |
| Jaw, Edentulous | |
| Rheumatic Heart Disease | A heart valve disease that is characterized by repeated inflammation with fibrinous repair. The cardinal anatomic changes of the valve include leaflet thickening, commissural fusion, and shortening and thickening of the tendinous cords.It is caused by an autoimmune reaction to Group A beta-hemolytic streptococci (GAS) that results in valvular damage. |
| Vascular Malformations | |
| Malaria, Cerebral | |
| Conjunctival Neoplasms | |
| Pleural Neoplasms | |
| Hip Dislocation | Displacement of the femur from its normal location in the hip joint. |
| Uterine Diseases | |
| 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. |
| Hypoxia-Ischemia, Brain | |
| Anxiety Disorders | |
| Acidosis, Lactic | |
| Glossitis, Benign Migratory | |
| Pregnancy Complications, Parasitic | |
| Myopathies, Nemaline | |
| Tongue, Fissured | OMIM mapping confirmed by DO. [SN]. |
| Environmental Illness | A syndrome that is an adverse physical reaction to low levels of many common chemicals. |
| Problem Solving | |
| Smell | |
| Arteritis | Arterial inflammation. |
| Torticollis | |
| Klippel-Trenaunay-Weber Syndrome | A rare congenital syndrome characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. |
| Migraine without Aura | A migraine that is characterized by migraine headaches that are not accompanied by an aura. |
| Field Dependence-Independence | |
| Hyperplasia | An abnormal increase in the number of cells in an organ or a tissue with consequent enlargement.|An abnormal increase in the number of (otherwise normal) cells in an organ or a tissue with consequent enlargement. |
| Hypoventilation | A reduction in the amount of air transported into the pulmonary alveoli by breathing, leading to hypercapnia (increase in the partial pressure of carbon dioxide). |
| Genetics, Behavioral | |
| Tay-Sachs Disease | OMIM mapping confirmed by DO. [SN]. |
| Abortion, Habitual | |
| Respiratory Tract Neoplasms | |
| 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. |
| Acrocephalosyndactylia | A synostosis that results_in craniosynostosis and syndactyly. |
| Infant, Premature, Diseases | |
| Endolymphatic Hydrops | |
| Keratoacanthoma | |
| Tuberculosis, Lymph Node | |
| Otitis Media | A otitis which involves inflammation of the middle ear. |
| Leukemia, Prolymphocytic | |
| Hearing | |
| Pseudomyxoma Peritonei | An appendix cancer that is characterized by progressive accumulation of mucus-secreting tumor cells within the abdomen and pelvis. |
| Ventricular Dysfunction | |
| Pelvic Organ Prolapse | Abnormal descent of a pelvic organ resulting in the protrusion of the organ beyond its normal anatomical confines. |
| Hyponatremia | An abnormally decreased sodium concentration in the blood. |
| Gonadal Dysgenesis | A hypogonadism that is characterized by a progressive loss of germ cells on the developing gonads of an embryo. |
| Neurotoxicity Syndromes | |
| Intracranial Arterial Diseases | |
| Phobic Disorders | |
| Dental Pulp Diseases | |
| Fragile X Syndrome | A neurodegenerative disease that is characterized by moderate to severe mental retardation, macroorchidism, and distinct facial features, including long face, large ears, and prominent jaw, and has_material_basis_in a loss of FMR1 function. |
| Gingival Recession | |
| Spina Bifida Occulta | The closed form of spina bifida with incomplete closure of a vertebral body with intact overlying skin. |
| Nasal Obstruction | Reduced ability to pass air through the nasal cavity often leading to mouth breathing. |
| Plasmacytoma | |
| Trichomonas Infections | |
| Leukemia, Myeloid, Chronic | |
| Bites and Stings | |
| Oral Submucous Fibrosis | |
| Hyperhidrosis | Abnormal excessive perspiration (sweating). |
| Drug Hypersensitivity | |
| Premature Birth | The birth of a baby of less than 37 weeks of gestational age. |
| Behcet Syndrome | A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis. |
| Measles | A viral infectious disease that results_in infection located_in skin, has_material_basis_in Measles virus, which is transmitted_by contact with oronasal secretions, or semen of an infected person. The infection has_symptom fever, has_symptom cough, has_symptom coryza, has_symptom conjunctivitis, and has_symptom maculopapular, erythematous rash. |
| Polyarteritis Nodosa | |
| Somatoform Disorders | |
| Q-Sort | |
| Heart Valve Diseases | |
| Graves Ophthalmopathy | |
| Pain Threshold | |
| Birth Weight | The mass or quantity of heaviness of an individual at BIRTH. It is expressed by units of pounds or kilograms. |
| Sleep Deprivation | |
| Influenza, Human | |
| Bernard-Soulier Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Fibromatosis, Abdominal | |
| Pulmonary Valve Stenosis | |
| Folic Acid Deficiency | |
| Telangiectasis | |
| Endocardial Cushion Defects | |
| Lymphoma, Large-Cell, Diffuse | |
| Association Learning | |
| 46, XY Disorders of Sex Development | |
| Coronary Aneurysm | |
| Dermatitis, Contact | |
| Retinal Dystrophies | |
| Sleep Arousal Disorders | |
| Refractive Errors | |
| Lymphoma, B-Cell | |
| Myelofibrosis | A myeloma that is located_in the bone marrow which results_in bone marrow being replaced by fibrous (scar) tissue. |
| Dog Diseases | |
| Carcinoma, Ductal, Breast | |
| Multiple Sclerosis, Relapsing-Remitting | |
| Vitamin B 12 Deficiency | A vitamin metabolic disorder that results from low blood levels of vitamin B12. |
| Hot Flashes | |
| Diabetic Nephropathies | |
| Embolism, Cholesterol | |
| Thyroid Neoplasms | |
| Cholesteatoma | |
| Liver Cirrhosis, Alcoholic | |
| Dysmenorrhea | Pain during menstruation that interferes with daily activities. |
| Hypothyroidism | A deficiency of thyroid hormone. |
| Ocular Hypertension | |
| Aging, Premature | |
| Graves Disease | An autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located_in thyroid gland. |
| Hematuria | The presence of blood in the urine. Hematuria may be gross hematuria (visible to the naked eye) or microscopic hematuria (detected by dipstick or microscopic examination of the urine). |
| Pancreatitis, Alcoholic | |
| Verbal Learning | |
| Alopecia | A hypotrichosis that is characterized by a loss of hair from the head or body. |
| Aortic Aneurysm, Thoracic | |
| Pancreatic Cyst | A cyst of the pancreas that possess a lining of mucous epithelium. |
| Arthritis | Arthritis (from Greek arthro-, joint + -itis, inflammation; plural: arthritides) is a form of joint disorder that involves inflammation of one or more joints. |
| Urinary Calculi | caliculi, or a solid concretion or crystal aggregation, found in the urinary bladder; often embedded in a glycoprotein matrix which may also contain some nonglycoproteins when associated with infection |
| Shoulder Dislocation | A displacement or misalignment of the humerus with respect to the other bones of the should joint. Note that a subluxation is a partial dislocation. |
| Reflex Sympathetic Dystrophy | OMIM mapping confirmed by DO. [SN]. |
| Radiation Injuries | |
| Spinal Dysraphism | OMIM mapping confirmed by DO. [LS]. |
| Carotid Artery Thrombosis | |
| Reflex, Abnormal | |
| Lymphoma | A malignant (clonal) proliferation of B- lymphocytes or T- lymphocytes which involves the lymph nodes, bone marrow and/or extranodal sites. This category includes Non-Hodgkin lymphomas and Hodgkin lymphomas.|A cancer that affects lymphocytes that reside in the lymphatic system and in blood-forming organs.|A general term for various neoplastic diseases of the lymphoid tissue.|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. |
| Septo-Optic Dysplasia | Underdevelopment of the optic nerve and absence of the septum pellucidum. |
| Mycetoma | |
| Kidney Failure | A kidney disease characterized by the failure of the kidneys to adequately filter waste products from the blood. |
| Ductus Arteriosus, Patent | |
| Postoperative Nausea and Vomiting | Emesis and queasiness occurring after anesthesia. |
| Pain, Postoperative | |
| Dengue Hemorrhagic Fever | A dengue disease that occurs when a person experiences a second infection with a heterologous Dengue virus serotype, which is transmitted_by Aedes mosquito bite. The infection has_symptom hemorrhagic lesions of the skin, has_symptom thrombocytopenia, has_symptom reduction in the fluid part of the blood, and has_symptom high fever. |
| Gastrointestinal Stromal Tumors | |
| Hepatic Veno-Occlusive Disease | |
| Plaque, Atherosclerotic | |
| Cystadenoma, Serous | |
| Ameloblastoma | A cell type benign neoplasm that has_material_basis_in odontogenic epithelium. |
| Pleural Diseases | |
| Maxillary Neoplasms | |
| Bone Diseases, Metabolic | |
| Low Back Pain | An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the lower back. |
| Hemorrhagic Fever, Ebola | |
| 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)|A malignant mesenchymal tumor arising from the bone.|A usually aggressive malignant bone-forming mesenchymal tumor, predominantly affecting adolescents and young adults. It usually involves bones and less frequently extraosseous sites. It often involves the long bones (particularly distal femur, proximal tibia, and proximal humerus). Pain with or without a palpable mass is the most frequent clinical symptom. It may spread to other anatomic sites, particularly the lungs. |
| Dental Plaque | A soft, thin film of food debris, mucin, and dead epithelial cells deposited on the teeth, providing the medium for the growth of various bacteria. The main inorganic components are calcium and phosphorus, with small amounts of magnesium, potassium, and sodium; the organic matrix consists of polysaccharides, proteins, carbohydrates, lipids, and other components. Plaque plays an important etiologic role in the development of dental caries and periodontal and gingival diseases and provides the base for the development of materia alba; calcified plaque forms dental calculus. |
| Skin Ulcer | A discontinuity of the skin exhibiting complete loss of the epidermis and often portions of the dermis and even subcutaneous fat. |
| Hantavirus Pulmonary Syndrome | A viral infectious disease that results_in infection located_in lung, has_material_basis_in Sin Nombre virus, transmitted_by deer mouse (Myodes glareolus), has_material_basis_in Black Creek Canal virus, transmitted_by cotton rat (Sigmodon hispidus), has_material_basis_in Bayou virus, transmitted_by marsh rice rat (Oryzomys palustris), has_material_basis_in Laguna Negra virus, transmitted_by small vesper mouse (Calomys laucha), or has_material_basis_in Andes virus, transmitted_by rice rat (Oligoryzomys longicaudatus). The infection has_symptom fever, has_symptom muscle pain, has_symptom headache, has_symptom cough, has_symptom vomiting, has_symptom chills which rapidly progress to bilateral interstitial pulmonary infiltrates occurrence, pulmonary edema and hypoxia often resulting in death from shock or cardiac complications. |
| Brain Edema | |
| Abdominal Neoplasms | |
| Nervous System Neoplasms | |
| Hypotension, Orthostatic | |
| Pain Insensitivity, Congenital | |
| Coxsackievirus Infections | |
| Tourette Syndrome | A tic disorder that is characterized by multiple physical (motor) tics and at least one vocal (phonic) tic present for more than a year. |
| Anophthalmos | |
| Urogenital Neoplasms | Tumors or cancer of the UROGENITAL SYSTEM in either the male or the female. |
| Fanconi Anemia | A congenital hypoplastic anemia characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. It is a result of a genetic defect in a cluster of proteins responsible for DNA repair. |
| Anemia, Pernicious | OMIM mapping confirmed by DO. [SN]. |
| Endocarditis, Bacterial | |
| Bronchopulmonary Dysplasia | Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring. |
| Wolff-Parkinson-White Syndrome | A disorder of the cardiac conduction system of the heart characterized by ventricular preexcitation due to the presence of an abnormal accessory atrioventricular electrical conduction pathway. |
| Chromosome Inversion | |
| Femoral Fractures | |
| Anemia, Hemolytic | |
| Landau-Kleffner Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Anemia, Hemolytic, Congenital | |
| Olfactory Perception | |
| Triploidy | |
| Osteoma | Osteomas are bony growths found most commonly on the skull and mandible; however, they may occur in any bone of the body. Osteomas do not usually cause clinical problems and do not become malignant. |
| Sleep Apnea, Obstructive | |
| Hemoglobin C Disease | |
| Hyperphagia | A neurological anomaly with gross overeating associated with an abnormally strong desire or need to eat. |
| Mental Disorders | |
| Optic Atrophies, Hereditary | |
| Hypotension | Blood pressure that is abnormally low. |
| Respiratory Tract Infections | |
| Arthralgia | Joint pain. |
| Post-Concussion Syndrome | |
| Neoplasms, Gonadal Tissue | |
| Glycogen Storage Disease Type II | A glycogen storage disease that has_material_basis_in deficiency of the lysosomal acid alpha-glucosidase enzyme resulting in damage to muscle and nerve cells due to an accumulation of glycogen in the lysosome. |
| Skin Diseases, Genetic | |
| Pulmonary Emphysema | |
| Occupational Diseases | |
| Cell Transformation, Viral | |
| Mental Competency | |
| Adenoma, Chromophobe | |
| Eyelid Diseases | |
| Sleep Apnea Syndromes | |
| Affective Disorders, Psychotic | |
| Astrocytoma | A glial tumor of the brain or spinal cord showing astrocytic differentiation. It includes the following clinicopathological entities: pilocytic astrocytoma, diffuse astrocytoma, anaplastic astrocytoma, pleomorphic xanthoastrocytoma, subependymal giant cell astrocytoma, and glioblastoma.|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 (MeSH).|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) |
| Skin Diseases, Viral | |
| Ectodermal Dysplasia | Ectodermal dysplasia is a group of conditions in which there is abnormal development of the skin, hair, nails, teeth, or sweat glands. |
| Flaviviridae Infections | |
| Leukemia, Lymphocytic, Acute | |
| Biliary Atresia | A cholestasis characterized by blockage of the ducts that carry bile from the liver to the gallbladder. |
| Paranoid Disorders | |
| Touch Perception | |
| Catastrophic Illness | |
| Lactose Intolerance | OMIM mapping confirmed by DO. [SN]. |
| Muscle Neoplasms | |
| Nutrition Disorders | |
| Tooth Loss | |
| Prenatal Exposure Delayed Effects | |
| Learning Disorders | |
| Tympanic Membrane Perforation | |
| Thinness | |
| Neuroacanthocytosis | |
| Mucopolysaccharidosis I | A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme alpha-L-iduronidase. |
| Diabetes Mellitus, Lipoatrophic | |
| Clubfoot | OMIM mapping confirmed by DO. [SN]. |
| Tonsillar Neoplasms | |
| Menorrhagia | Excessive uterine bleeding during MENSTRUATION. |
| Ventricular Fibrillation | Uncontrolled contractions of muscles fibers in the left ventricle not producing contraction of the left ventricle. Ventricular fibrillation usually begins with a ventricular premature contraction and a short run of rapid ventricular tachycardia degenerating into uncoordinating ventricular fibrillations. |
| Hyperlipoproteinemia Type I | |
| Mental Health Services | |
| Neurodegenerative Diseases | |
| Myxedema | OMIM mapping confirmed by DO. [SN]. |
| Introversion | |
| Rectal Prolapse | |
| Impotence | |
| Yin Deficiency | |
| Schistosomiasis | A parasitic helminthiasis infectious disease that involves infection of the intestine, urinary tract, skin, liver and spleen caused by multiple species of the trematode fluke of the genus Schistosoma. The symptoms include fever, chills, nausea, abdominal pain, diarrhea, malaise, myalgia, liver and spleen enlargement, rash and hematuria. |
| Carcinoma in Situ | |
| Startle Reaction | |
| Giant Cell Arteritis | OMIM mapping confirmed by DO. [LS]. |
| Osteopetrosis | An osteosclerosis that has_material_basis_in lack of bone resorption which results_in abnormally hard and brittle bones. |
| Rhabdomyosarcoma, Alveolar | |
| Celiac Disease | A food allergy that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite.|A malabsorption syndrome that is precipitated by the ingestion of GLUTEN-containing foods, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION.|A food hypersensitivity that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite.|A malabsorption syndrome that is precipitated by the ingestion of foods containing GLUTEN, such as wheat, rye, and barley. It is characterized by INFLAMMATION of the SMALL INTESTINE, loss of MICROVILLI structure, failed INTESTINAL ABSORPTION, and MALNUTRITION. |
| Intestinal Fistula | An abnormal connection between the gut and another hollow organ, such as the bladder, urethra, vagina, or other regions of the gastrointestinal tract. |
| Tuberculosis, Meningeal | |
| Lymphoma, T-Cell, Cutaneous | |
| Hypertrophy, Right Ventricular | |
| Ectopia Lentis | Dislocation or malposition of the crystalline lens of the eye. A partial displacement (or dislocation) of the lens is described as a subluxation of the lens, while a complete displacement is termed luxation of the lens. A complete displacement occurs if the lens is completely outside the patellar fossa of the lens, either in the anterior chamber, in the vitreous, or directly on the retina. If the lens is partially displaced but still contained within the lens space, then it is termed subluxation. |
| Opisthorchiasis | A parasitic helminthiasis infectious disease that involves parasitic infection of the liver, pancreas and gall bladder by Opisthorchis viverrini or Opisthorchis felineus. The symptoms include dyspepsia, abdominal pain, diarrhea, constipation, hepatomegaly, cholangitis, cholecystitis, and chlolangiocarcinoma. |
| Apraxias | |
| Genetic Predisposition to Disease | |
| Asphyxia Neonatorum | |
| Mucopolysaccharidosis II | A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase. |
| Arthritis, Experimental | |
| Dysthymic Disorder | A mood disorder that involves the presence of a low mood almost daily over a span of at least two years. |
| Wechsler Scales | |
| Adrenal Hyperplasia, Congenital | |
| Genital Neoplasms, Female | |
| Spondylitis, Ankylosing | |
| Angina Pectoris, Variant | |
| Kidney Failure, Acute | |
| Hydrops Fetalis | The abnormal accumulation of fluid in two or more fetal compartments, including ascites, pleural effusion, pericardial effusion, and skin edema. |
| Vasculitis, Allergic Cutaneous | |
| Exanthema | |
| Lung Diseases, Obstructive | |
| Sebaceous Gland Neoplasms | |
| Mastocytosis, Cutaneous | |
| Pheochromocytoma | Pheochromocytomas (also known as chromaffin tumors) produce, store, and secrete catecholamines. Pheochromocytomas usually originate from the adrenal medulla but may also develop from chromaffin cells in or about sympathetic ganglia. A common symptom of pheochromocytoma is hypertension owing to release of catecholamines. |
| Acidosis, Renal Tubular | |
| Pancytopenia | |
| Agranulocytosis | |
| Memory, Long-Term | |
| Varicocele | |
| Loudness Perception | |
| von Willebrand Disease | A coagulation protein disease that is a hereditary abnormality which slows the blood clotting process. It arises from a qualitative or quantitative deficiency of von Willebrand factor (vWF), a multimeric protein that is required for platelet adhesion. |
| Coronary Disease | Thickening and loss of elasticity of the CORONARY ARTERIES, leading to progressive arterial insufficiency (CORONARY DISEASE).|Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause.|Narrowing of the coronary arteries due to fatty deposits inside the arterial walls.|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. |
| Frontotemporal Lobar Degeneration | A basal ganglia disease characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language. |
| Fatigue Syndrome, Chronic | |
| Neoplasms, Experimental | |
| Pulmonary Blastoma | An embryoma and malignant neoplasm of lung that derives_from tissues of the lung and derives_from pleura (a thin layer of tissue that covers the lungs and lines the interior wall of the chest cavity). It is most commonly effects children. |
| Brain Infarction | |
| Cardiomyopathy, Alcoholic | |
| Lafora Disease | OMIM mapping confirmed by DO. [SN]. |
| Hypesthesia | |
| Alcoholic Intoxication | |
| Osteoradionecrosis | |
| Resilience, Psychological | |
| Pemphigus | |
| Parkinson Disease, Secondary | |
| Intervertebral Disk Displacement | |
| Polyradiculoneuropathy, Chronic Inflammatory Demyelinating | |
| Ischemic Attack, Transient | |
| Agammaglobulinemia | A B cell deficiency that is caused by a reduction in all types of gamma globulins. |
| Cardiac Output, Low | |
| Carcinosarcoma | A mixed cell type cancer that has_material_basis_in carcinomatous (epithelial tissue) and sarcomatous (connective tissue) components. |
| Adenoma, Oxyphilic | |
| Epilepsy | A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions. |
| Growth Disorders | |
| Mucolipidoses | |
| Mitochondrial Diseases | |
| Inappropriate ADH Syndrome | |
| Labor Pain | |
| Mucopolysaccharidosis VII | A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme beta-glucuronidase resulting in the inability to degrade glucuronic acid-containing glycosaminoglycans. |
| Bone Diseases, Developmental | |
| Gallbladder Diseases | |
| Herpes Genitalis | A herpes simplex that results_in infection located_in genital system, or located_in rectum, has_material_basis_in Human herpesvirus 1 or has_material_basis_in Human herpesvirus 2, which is transmitted_by sexual contact. The infection has_symptom sores, has_symptom fever, and has_symptom swollen glands. |
| Wolman Disease | |
| Postoperative Complications | |
| Heroin Dependence | An opiate dependence that involves the continued use of heroin despite problems related to use of the substance. |
| Multicystic Dysplastic Kidney | Multicystic dysplasia of the kidney is characterized by multiple cysts of varying size in the kidney and the absence of a normal pelvocaliceal system. The condition is associated with ureteral or ureteropelvic atresia, and the affected kidney is nonfunctional. |
| Mutism | A speech disorder that involves a complete inability to speak. |
| Diabetic Angiopathies | |
| Reaction Time | |
| Intracranial Arteriosclerosis | |
| Anemia, Diamond-Blackfan | |
| Nephrocalcinosis | |
| Hepatic Encephalopathy | |
| Exostoses, Multiple Hereditary | |
| Facial Paralysis | |
| Cholestasis, Intrahepatic | |
| Cardiomegaly | Increased size of the heart. |
| Renal Insufficiency, Acute | |
| Myelodysplastic Syndromes | |
| Tracheoesophageal Fistula | An abnormal connection (fistula) between the esophagus and the trachea. |
| Dyskeratosis Congenita | A skin disease characterized by cutaneous pigmentation, premature graying, dystrophy of the nails, leukoplakia of the oral mucosa, continuous lacrimation due to atresia of the lacrimal ducts, often thrombocytopenia, anemia, testicular atrophy in the male carriers and predisposition to cancer. |
| Stress Disorders, Post-Traumatic | |
| Intracranial Thrombosis | |
| Brain Stem Neoplasms | |
| Liver Abscess | The presence of an abscess of the liver. |
| Eye Diseases | |
| Immunoblastic Lymphadenopathy | |
| Optic Nerve Glioma | |
| Enteritis | |
| Malignant Hyperthermia | A genetic disease that is characterized by a drastic and uncontrolled increase in skeletal muscle oxidative metabolism, which overwhelms the body's capacity to supply oxygen, remove carbon dioxide, and regulate body temperature. |
| Retinal Diseases | |
| Seizures, Febrile | |
| Signal Detection, Psychological | |
| Nevus, Pigmented | |
| Vision Disorders | |
| Osteochondrodysplasias | |
| Abnormalities, Multiple | |
| Condylomata Acuminata | |
| Lymphadenitis | |
| Neurotic Disorders | |
| Aortic Aneurysm, Abdominal | |
| Keratoconjunctivitis | |
| Pleurisy | A pleural disease that is characterized by inflammation of the pleura, the lining of the pleural cavity surrounding the lungs. |
| Alveolitis, Extrinsic Allergic | |
| Syndactyly | A synostosis that results_in the fusion of two or more digits. |
| Clonorchiasis | A parasitic helminthiasis infectious disease that involves parasitic infection of the bile ducts of the liver by Clonorchis sinensis. The symptoms include abdominal pain, nausea, diarrhea, and eosinophilia. In long-standing infections, cholangitis, cholelithiasis, pancreatitis, and cholangiocarcinoma can develop. |
| Sarcoidosis | A hypersensitivity reaction type IV disease characterized by the growth of collections of inflammatory cells (granulomas) in multiple organs. |
| Bulbar Palsy, Progressive | |
| MERRF Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Muscular Dystrophy, Emery-Dreifuss | |
| Hamartoma Syndrome, Multiple | |
| Neoplasms, Nerve Tissue | |
| Pulmonary Eosinophilia | |
| Personality Tests | |
| Polycystic Kidney, Autosomal Recessive | |
| Fish Diseases | |
| Toxoplasmosis | A coccidiosis that has_material_basis_in protozoan Toxoplasma gondii. The parasite effects most genera of warm-blooded animals, including humans, but the primary host is the felid (cat) family. Animals are infected by eating infected meat, by ingestion of feces of a cat that has itself recently been infected, or transmission_by mother to fetus. The symptoms include bilateral, nontender cervical or axillary lymphadenopathy, fever, malaise, myalgia, hepatosplenomegaly, anemia and leukopenia. |
| Encephalomyelitis, Autoimmune, Experimental | An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5) |
| Epilepsy, Reflex | |
| Helicobacter Infections | |
| Streptococcal Infections | |
| Vasculitis, Central Nervous System | |
| Giant Cell Tumors | |
| Familial Mediterranean Fever | A hypersensitivity reaction type II disease characterized by recurrent episodes of fever and acute inflammation of the membranes lining the abdomen, joints and lungs; caused by mutations in the MEFV gene, which encodes the protein pyrin. |
| Dystonia Musculorum Deformans | A dystonia that affects most or all of the body. |
| Supranuclear Palsy, Progressive | |
| Porphyria Cutanea Tarda | An acute porphyria characterized by painful, blistering skin lesions that develop on sun-exposed skin. |
| Emergencies | |
| Dental Fistula | |
| Cystadenocarcinoma, Serous | |
| Tooth Diseases | |
| Syncope, Vasovagal | |
| Respiration Disorders | |
| Nocturnal Myoclonus Syndrome | |
| Heart Rupture | |
| Mesopic Vision | |
| Task Performance and Analysis | |
| Head Injuries, Penetrating | |
| Dysgeusia | |
| Ehlers-Danlos Syndrome | A collagen disease and a monogenic disease that is characterized by extremely flexible joints, elastic skin, and excessive bruising caused by a heritable defect in collagen synthesis, which leads to marked healing difficulties. EDS has five cardinal signs, which may be present to some degree in all of the subtypes. These five cardinal signs are skin fragility, blood vessel fragility, skin hyperelasticity, joint hypermobility, and characteristic subcutaneous nodules. |
| Cell Transformation, Neoplastic | |
| Tumor 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).|A Herpesviridae infectious disease that results_in infection, has_agent Human herpesvirus 4, which is transmitted_by contact with the saliva. |
| Renal Artery Obstruction | |
| Pancreatic Neoplasms | |
| Hypophosphatemic Rickets, X-Linked Dominant | A metal metabolism disorder that results from the inactivation of hormone-like substances (phosphatonins) that promote phosphate excretion which has_material_basis_in a X-linked mutation in the PHEX gene. |
| Brain Neoplasms | |
| Bulimia Nervosa | An eating disorder that is characterized by a cycle of binge eating (BULIMIA or bingeing) followed by inappropriate acts (purging) to avert weight gain. Purging methods often include self-induced VOMITING, use of LAXATIVES or DIURETICS, excessive exercise, and FASTING. |
| Keratitis | |
| Focal Epithelial Hyperplasia | A viral infectious disease that results_in infection located_in mouth, has_material_basis_in human papillomavirus (types 13 or 32), has_symptom papules or nodules in the oral cavity. |
| Arthritis, Infectious | |
| Anthrax | |
| Acute Disease | |
| Urogenital Abnormalities | The presence of any abnormality of the genitourinary system. |
| Ichthyosiform Erythroderma, Congenital | |
| Radiation Pneumonitis | |
| Candidiasis, Vulvovaginal | |
| Urologic Neoplasms | |
| Neoplasm Metastasis | |
| Taste Disorders | |
| Bone Marrow Neoplasms | |
| Dyskinesias | |
| 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. |
| Pituitary ACTH Hypersecretion | |
| Malaria | A protozoan disease caused in humans by four species of the PLASMODIUM genus: PLASMODIUM FALCIPARUM; PLASMODIUM VIVAX; PLASMODIUM OVALE; and PLASMODIUM MALARIAE; and transmitted by the bite of an infected female mosquito of the genus ANOPHELES. Malaria is endemic in parts of Asia, Africa, Central and South America, Oceania, and certain Caribbean islands. It is characterized by extreme exhaustion associated with paroxysms of high FEVER; SWEATING; shaking CHILLS; and ANEMIA. Malaria in ANIMALS is caused by other species of plasmodia.|Malaria is a parasitic disease characterized as a vector-borne arthropod infectious acute or chronic disease caused by the presence of sporozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle. Occurrance is widespread in tropical and subtropical regions, including parts of the Americas, Asia, and Africa.|A protozoan infection caused by the genus Plasmodium. There are four species of Plasmodium that can infect humans: Plasmodium falciparum, vivax, ovale, and malariae. It is transmitted to humans by infected mosquitoes. Signs and symptoms include paroxysmal high fever, sweating, chills, and anemia.|An Aconoidasida infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle. |
| Ileus | |
| Urticaria Pigmentosa | OMIM mapping confirmed by DO. [LS]. |
| Granuloma | |
| Chagas Disease | A trypanosomiasis that is a tropical parasitic disease caused by the flagellate protozoan Trypanosoma cruzi, which is transmitted to humans and other mammals by an insect vector, the blood-sucking assassin bugs of the subfamily Triatominae (family Reduviidae), most commonly species belonging to the Triatoma, Rhodnius, and Panstrongylus genera. The symptoms include fever, fatigue, body aches, headache, rash, loss of appetite, diarrhea, vomiting, swelling of the eyelids and myocarditis. |
| Plague | A primary bacterial infectious disease that results_in infection, located_in lymph node, located_in vasculature or located_in lungs, has_material_basis_in Yersinia pestis, which is transmitted_by oriental rat flea (Xenopsylla cheopis) infected by feeding on rodents and other mammals, transmitted_by air, transmitted_by direct contact or transmitted_by ingestion of contaminated undercooked food. |
| Sex Chromosome Aberrations | |
| Weight Gain | |
| Sotos Syndrome | An autosomal recessive disease that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life. |
| Chromosome Deletion | |
| Inversion, Chromosome | |
| Multiple Endocrine Neoplasia Type 1 | An autosomal dominant disease that has_material_basis_in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas. |
| Hearing Disorders | |
| Angioedemas, Hereditary | |
| Leiomyoma | A cell type benign neoplasm that is a benign tumor of smooth muscle cells. |
| Uncertainty | |
| Nasopharyngitis | A nasopharyngeal disease which involves inflammation of the nasal passages and upper part of the pharynx. |
| Bronchopulmonary Sequestration | The presence of microscopic cystic masses of nonfunctioning pulmonary tissue that lack an obvious communication with the tracheobronchial tree. |
| Seminoma | A germinoma that has_material_basis_in cells that make sperm and eggs. |
| Hematologic Diseases | |
| Albinism, Oculocutaneous | |
| Cytomegalovirus Retinitis | |
| Tuberous Sclerosis | OMIM mapping confirmed by DO. [LS]. |
| Paraparesis, Spastic | |
| Intuition | Knowing or understanding without conscious use of reasoning. (Thesaurus of ERIC Descriptors, 1994) |
| Psychotherapy, Brief | |
| Focal Nodular Hyperplasia | |
| Transfer | |
| Postmortem Changes | |
| Anti-Glomerular Basement Membrane Disease | A hypersensitivity reaction type II disease that is characterized by glomerulonephritis located_in kidney and hemorrhaging located_in lung. |
| Citrullinemia | An urea cycle disorder that involves the accumulation of ammonia in the blood. |
| Mouth Diseases | |
| Postural Orthostatic Tachycardia Syndrome | |
| Touch | |
| Adenofibroma | A cell type benign neoplasm that is composed_of glandular and fibrous tissues, with a relatively large proportion of glands. |
| Thymus Neoplasms | |
| Smallpox | A viral infectious disease that results_in infection located_in skin, has_material_basis_in Variola virus, which is transmitted_by droplets from oral, nasal or pharyngeal mucosa, transmitted_by contact with the body fluids, or transmitted_by fomites. The infection results_in_formation_of lesions, first on the face, hands and forearms and later on the trunk. |
| Infarction, Middle Cerebral Artery | |
| Religion and Psychology | |
| Fabry Disease | OMIM mapping confirmed by DO. [SN]. |
| Encephalitis, Japanese | |
| Calculi | |
| Rhabdomyosarcoma, Embryonal | |
| Myoclonus | Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements. |
| Sleep Apnea, Central | |
| Periapical Diseases | |
| Aortitis | |
| Prosthesis Failure | |
| Hepatitis B, Chronic | |
| Cysts | |
| Hypercalciuria | |
| Atherosclerosis | A thickening and loss of elasticity of the walls of ARTERIES that occurs with formation of ATHEROSCLEROTIC PLAQUES within the ARTERIAL INTIMA. |
| Cross Infection | |
| Hepatomegaly | Abnormally increased size of the liver. |
| Aphasia | A language disorder that involves an acquired impairment of any laguage modality such as producting or comprehending spoken or written language. |
| Conjunctivitis, Allergic | |
| Atrophy | |
| De Lange Syndrome | A genetic disease that is characterized by slow growth before and after birth, intellectual disability that is usually severe to profound, skeletal abnormalities involving the arms and hands, and distinctive facial features. |
| Inhibition | |
| Voice Disorders | |
| Candidiasis, Oral | |
| Nail Diseases | |
| Scoliosis | An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed) |
| Neurofibroma, Plexiform | |
| Amenorrhea | |
| Smoke Inhalation Injury | |
| Kuru | |
| Mycobacterium Infections, Atypical | |
| Bone Marrow Diseases | |
| Hernia, Umbilical | |
| Sacroiliitis | |
| Ovarian Diseases | |
| Choline Deficiency | |
| Sensation | |
| Neoplasm Circulating Cells | |
| Lymphoma, AIDS-Related | |
| Meningitis, Cryptococcal | |
| Kearns-Sayer Syndrome | |
| Rheumatoid Nodule | |
| Dermatomyositis | A myositis and is_a dermatitis that results_in inflammation located_in muscle and located_in skin. The disease may result from either a viral infection or an autoimmune reaction.|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) |
| Urea Cycle Disorders, Inborn | |
| Joint Instability | |
| Coagulation Protein Disorders | |
| Eye Neoplasms | |
| Leukemia, Myelomonocytic, Acute | |
| Paraganglioma, Extra-Adrenal | |
| Lymphoma, Mucosa-Associated Lymphoid Tissue | |
| Cartilage Diseases | |
| Paraneoplastic Syndromes, Nervous System | |
| Esophagitis | |
| Postpoliomyelitis Syndrome | A poliomyelitis that results_in atrophy located_in muscle, many years after the initial infection, has_material_basis_in Human poliovirus 1, has_material_basis_in Human poliovirus 2, or has_material_basis_in Human poliovirus 3. It is characterized by new weakening in muscles that were previously affected by the polio infection and in muscles that were unaffected. The infection has_symptom muscle weakness, has_symptom muscle pain, has_symptom sleep apnea, and has_symptom breathing problems. |
| Leukemia, Erythroblastic, Acute | |
| Usher Syndromes | |
| Pseudohypoparathyroidism | OMIM mapping confirmed by DO. [SN]. |
| Epidermodysplasia Verruciformis | An autosomal recessive disease that results_in skin squamous cell carcinoma located_in skin, associated with a high risk of carcinoma. It is characterized by abnormal susceptibility to human papillomaviruses of the skin and has_symptom lesions on the body. |
| Nerve Sheath Neoplasms | |
| Depression, Postpartum | |
| Cystitis | |
| Coronary Restenosis | |
| Posterior Tibial Tendon Dysfunction | |
| Legionnaires' Disease | A legionellosis that is characterized by severe form of infection producing pneumonia. Symptoms include fever, chills, and cough. |
| Glucose Intolerance | |
| Conditioning | |
| Jaw Neoplasms | |
| Neoplasms, Unknown Primary | |
| Electroconvulsive Therapy | |
| Bloom Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Microvascular Angina | |
| Colitis, Ischemic | |
| Preleukemia | |
| Dyslipidemias | |
| Temporomandibular Joint Disorders | |
| Pericarditis | A pericardium disease that is characterized by an inflammation of the pericardium and has_symptom chest pain. |
| Marijuana Abuse | A substance abuse that involves the recurring use of cannabis despite negative consequences. |
| Porphyria, Acute Intermittent | |
| Genu Valgum | The legs angle inward, such that the knees are close together and the ankles far apart. |
| Mandibular Neoplasms | |
| Leukocytosis | An abnormal increase in the number of leukocytes in the blood. |
| Photosensitivity Disorders | |
| Angina, Unstable | |
| Enterocolitis | An inflammation of the colon and small intestine. However, most conditions are either categorized as Enteritis (inflammation of the small intestine) or Colitis (inflammation of the large intestine). |
| Alcohol-Induced Disorders | |
| Vitamin A Deficiency | |
| Somnambulism | |
| Serial Learning | |
| Renal Tubular Transport, Inborn Errors | |
| Diabetes Complications | |
| Cholestasis | |
| Postoperative Hemorrhage | |
| Encephalitis, Viral | An encephalitis that involves inflammation of the brain caused by viral infection. |
| Psychiatry | |
| Vulvar Neoplasms | |
| Conduct Disorder | A specific developmental disorder marked by a pattern of repetitive behavior wherein the rights of others or social norms are violated. |
| Hearing Loss, Unilateral | |
| Long QT Syndrome | An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles). |
| Diabetes, Gestational | |
| CADASIL | |
| Miosis | Abnormal (non-physiological) constriction of the pupil. |
| Tooth Demineralization | |
| Coloboma | An eye disease characterized by missing pieces of tissue in structures that form the eye, such as the iris, retina, choroid or optic disc. |
| Personality Assessment | |
| Endophthalmitis | A globe disease that is characterized by inflammation of the inside of the eye. |
| Cocaine-Related Disorders | |
| Persistent Fetal Circulation Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Mycoses | |
| Anticipation, Genetic | |
| Communicable Diseases | |
| Retinal Degeneration | |
| Myocarditis | An extrinsic cardiomyopathy that is characterized as an inflammation of the heart muscle. |
| Thalassemia | OMIM mapping confirmed by DO. [LS]. |
| Vulvovaginitis | |
| Hyperkinesis | Motor hyperactivity with excessive movement of muscles of the body as a whole. |
| Adenoma, Pleomorphic | |
| Neoplasms, Germ Cell and Embryonal | |
| Multiple Acyl Coenzyme A Dehydrogenase Deficiency | |
| Kidney Failure, Chronic | |
| Myeloproliferative Disorders | |
| Puberty, Precocious | |
| Pancreatitis, Chronic | |
| Jervell-Lange Nielsen Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Fractures, Spontaneous | |
| Disorders of Excessive Somnolence | |
| Carcinoid Tumor | A tumor formed from the endocrine (argentaffin) cells of the mucosal lining of a variety of organs including the stomach and intestine. These cells are from neuroectodermal origin. |
| Sarcoma | A usually aggressive malignant mesenchymal cell tumor most commonly arising from muscle, fat, fibrous tissue, bone, cartilage, and blood vessels. Sarcomas occur in both children and adults. The prognosis depends largely on the degree of differentiation (grade) of the tumor. Representative subtypes are liposarcoma, leiomyosarcoma, osteosarcoma, and chondrosarcoma.|A malignant mesenchymal neoplasm arising exclusively from the soft tissues. Representative examples include soft tissue sarcoma, extraosseous Ewing sarcoma/peripheral primitive neuroectodermal tumor, and malignant hemangiopericytoma.|Neoplasms developing from some structure of the connective and subcutaneous tissue. The concept does not refer to neoplasms located in connective or soft tissue.|A cancer that affects connective tissue resulting in mesoderm proliferation.|A malignant mesenchymal neoplasm arising from muscle tissue, adipose tissue, blood vessels, fibrous tissue, or other supportive tissues excluding the bones.|Type of cancer of the bone, cartilage, fat, muscle, blood vessels, or other connective or supportive tissue. |
| Retinal Vein Occlusion | |
| Epistaxis | Bleeding from the nose. |
| Leukoencephalopathies | |
| Papilloma, Choroid Plexus | |
| Eyelid Neoplasms | |
| Anemia, Megaloblastic | |
| Urinary Incontinence, Stress | |
| Lung Neoplasms | |
| Purine-Pyrimidine Metabolism, Inborn Errors | |
| Hypersensitivity, Delayed | |
| Hemosiderosis | An iron metabolism disease that has_material_basis_in an accumulation of hemosiderin, an iron-storage complex, resulting in iron overload. |
| Tinnitus | Tinnitus is an auditory perception that can be described as the experience of sound, in the ear or in the head, in the absence of external acoustic stimulation. |
| Purpura, Thrombocytopenic, Idiopathic | |
| Bowen's Disease | |
| Hodgkin Disease | A lymphoma that is marked by the presence of a type of cell called the Reed-Sternberg cell. |
| Carcinoma, Non-Small-Cell Lung | |
| Overdose | |
| Spondylosis | An bone structure disease that involves degeneration between vertebra located_in vertebral column. |
| Behavior Therapy | |
| Wounds and Injuries | |
| Rare Diseases | |
| Thymus Hyperplasia | Enlargement of the thymus. |
| Intestinal Obstruction | |
| Vaginal Diseases | |
| Genetic Determinism | |
| Cryptorchidism | Cryptorchidism (derived from the Greek κρυπτός, kryptos, meaning hidden and ὄρχις, orchis, meaning testicle) is the absence of one or both testes from the scrotum. It is the most common birth defect regarding male genitalia. In unique cases, cryptorchidism can develop later in life, often as late as young adulthood. About 3% of full-term and 30% of premature infant boys are born with at least one undescended testis. However, about 80% of cryptorchid testes descend by the first year of life (the majority within three months), making the true incidence of cryptorchidism around 1% overall. Cryptorchidism is distinct from monorchism the condition of having only one testicle. |
| Lymphatic Diseases | |
| Hyperlipoproteinemia Type III | |
| Drug-Induced Liver Injury | A spectrum of clinical liver diseases ranging from mild biochemical abnormalities to ACUTE LIVER FAILURE, caused by drugs, drug metabolites, and chemicals from the environment. |
| Churg-Strauss Syndrome | A vasculitits that is systemic vasculitis realized as blood vessel inflammation and has_symptom asthma along with hay fever, rash and gastrointestinal bleeding. |
| Leukemia, Nonlymphocytic, Acute | |
| Forearm Injuries | |
| Gastritis | A stomach disease that is an inflammation of the lining of the stomach. |
| Substance-Related Disorders | |
| Asthma, Aspirin-Induced | |
| Basal Ganglia Diseases | |
| Chlamydia Infections | |
| Rhinitis | A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip. |
| Anemia, Sickle Cell | |
| Gardner Syndrome | Gardner syndrome (GS) is a severe form of familial adenomatous polyposis (FAP, see this term) characterized by multiple adenomas in the colon and rectum associated with prominent extracolonic features including osteomas and multiple skin and soft tissue tumors (desmoid tumor; see this term). |
| Subarachnoid Hemorrhage | Hemorrhage occurring between the arachnoid mater and the pia mater. |
| Sleep Initiation and Maintenance Disorders | |
| Dermatitis, Atopic | |
| Death | A permanent cessation of all vital functions: the end of life; can be applied to a whole organism or to a part of an organism. |
| Severe Acute Respiratory Syndrome | A coronavirus infectious disease and is_a respiratory system infectious disease that results_in infection located_in respiratory tract, has_agent SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia.|Severe acute respiratory syndrome is a respiratory tract infection described as a severe respiratory illness that is transmitted especially by contact with infectious material (as respiratory droplets or body fluids), is caused by a single-stranded RNA virus of the genus Coronavirus (SARS-CoV), is characterized by fever, headache, body aches, a dry cough, and hypoxia and usually by pneumonia.|A respiratory system infectious disease and is_a coronavirus infectious disease that results_in infection located_in respiratory tract, has_agent SARS coronavirus (SARS-CoV), which is transmitted_by droplet spread of respiratory secretions, transmitted_by ingestion of contaminated food, or transmitted_by fomites. The infection has_symptom fever, has_symptom headache, has_symptom body aches, has_symptom dry cough, and has_symptom hypoxia.|A viral disorder characterized by high FEVER, dry COUGH, shortness of breath (DYSPNEA) or breathing difficulties, and atypical PNEUMONIA. A virus in the genus CORONAVIRUS is the suspected agent.|A respiratory system infectious disease that is a severe respiratory illness characterized by fever, headache, body aches, a dry cough, and hypoxia and pneumonia caused by a single-stranded RNA virus of the genus SARS coronavirus (SARS-CoV). |
| Exocrine Pancreatic Insufficiency | |
| Raynaud Disease | OMIM mapping confirmed by DO. [SN]. |
| Cleft Palate | An orofacial cleft characterized by a fissure of the soft and/or hard palate, due to faulty fusion of the two plates of the skull that form the hard palate. |
| Multiple Endocrine Neoplasia | |
| Self Mutilation | |
| Aneurysm, Dissecting | |
| Hyperandrogenism | |
| Leukemia, Monocytic, Acute | |
| Gastrointestinal Neoplasms | |
| Pain | An unpleasant sensation induced by noxious stimuli which are detected by NERVE ENDINGS of NOCICEPTIVE NEURONS. |
| Anticipation, Psychological | |
| Nevus, Blue | |
| Enterobacteriaceae Infections | |
| Peripheral Nervous System Diseases | |
| Negotiating | |
| Mediastinal Neoplasms | |
| Vitamin D Deficiency | |
| Anus Diseases | |
| Testicular Diseases | |
| Protein S Deficiency | |
| Pulmonary Fibrosis | |
| Factor V Deficiency | OMIM mapping confirmed by DO. [SN]. |
| Steroid Metabolism, Inborn Errors | |
| Dementia, Vascular | |
| Coronary Stenosis | |
| Pallister-Hall Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Cheilitis | A lip disease characterized by the inflammation of the lips; which may include the perioral skin, the vermilion border and the labial mucosa. |
| Fetal Weight | |
| Ophthalmoplegia | |
| Polycythemia Vera | |
| Ophthalmia, Sympathetic | |
| Filariasis | A parasitic helminthiasis infectious disease that involves parasitic infection of the lymphatics and subcutaneous tissue by nematodes of the superfamily Filarioidea. |
| Tricuspid Atresia | Failure to develop of the tricuspid valve and thus lack of the normal connection between the right atrium and the right ventricle. |
| Maple Syrup Urine Disease | An organic acidemia that is caused by a deficiency of decarboxylase leading to high concentrations of valine, leucine, isoleucine, and alloisoleucine in the blood, urine, and cerebrospinal fluid and characterized by an odor of maple syrup to the urine, vomiting, hypertonicity, severe mental retardation, seizures, and eventually death unless the condition is treated with dietary measures. |
| Delirium | |
| Combat Disorders | |
| Meningomyelocele | |
| Thyroid Nodule | Pathological nodule in the thyroid gland, often filled with colloid; some are indicative of adenoma or carcinoma. |
| Epilepsy, Rolandic | |
| Frasier Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Head Injuries, Closed | |
| Asperger Syndrome | An autism spectrum disorder that is characterized by significant difficulties in social interaction, along with restricted and repetitive patterns of behavior and interests. It differs from other autism spectrum disorders by its relative preservation of linguistic and cognitive development. |
| Granulosa Cell Tumor | |
| Bipolar Disorder | A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence.|A major affective disorder marked by severe mood swings (manic or major depressive episodes) and a tendency to remission and recurrence (MeSH). |
| Imagination | |
| Waardenburg's Syndrome | An autosomal disease characterized by varying degrees of deafness, minor defects in structures arising from the neural crest and pigmentation anomalies of the hair, the skin and/or the iris of both eyes. |
| Blepharoptosis | An eye disease characterized by the drooping or falling of the upper or lower eyelid. |
| Substance Abuse, Intravenous | |
| Abnormalities | |
| Compulsive Personality Disorder | |
| Tooth, Supernumerary | |
| Psychophysiologic Disorders | |
| Bronchiectasis | A bronchial disease that is a chronic inflammatory condition of one or more bronchi or bronchioles marked by dilatation and loss of elasticity of the walls resulting from damage to the airway wall leading to the formation of small sacs on the bronchial wall and impairment of cilia mobility in the lung. Inflammation of the bronchial wall increases mucus secretion which serves as a breeding ground for bacteria. Bronchiectasis is caused by repeated respiratory infections, immune deficiency disorders, hereditary disorders (cystic fibrosis or primary ciliary dyskinesia), mechanical factors (inhaled object or a lung tumor) or inhaling toxic substances. |
| Asthma | A chronic respiratory disease manifested as difficulty breathing due to the narrowing of bronchial passageways.|Tendency of the smooth muscle of the tracheobronchial tree to contract more intensely in response to a given stimulus than it does in the response seen in normal individuals. This condition is present in virtually all symptomatic patients with asthma. The most prominent manifestation of this smooth muscle contraction is a decrease in airway caliber that can be readily measured in the pulmonary function laboratory.|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).|A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors resulting in recurring periods of wheezing (a whistling sound while breathing), chest tightness, shortness of breath, mucus production and coughing. The symptoms appear due to a variety of triggers such as allergens, irritants, respiratory infections, weather changes, excercise, stress, reflux disease, medications, foods and emotional anxiety. |
| Aortic Valve Insufficiency | An aortic valve disease that is characterized by leaking of the aortic valve of the heart causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle. |
| Restless Legs Syndrome | A central nervous system disease characterized by throbbing, pulling creeping or other unpleasant sensations in the legs and the irresistible urge to move them. |
| Mitral Valve Insufficiency | |
| Periapical Abscess | |
| Dyslexia, Acquired | |
| Encephalocele | A neural tube defect characterized by sac-like protrusions of the brain and the membranes that cover it through openings in the skull. |
| Sinusitis | A paranasal sinus disease involving inflammation of the paranasal sinuses resulting from bacterial, fungal, viral infection, allergic or autoimmune issues. Symptoms can include fever, weakness, fatigue, cough and congestion. There may also be mucus drainage in the back of the throat, called postnasal drip. |
| Spirituality | |
| Narcolepsy | A sleep disorder that involves an excessive urge to sleep at inappropriate times, such as while at work. |
| Digestive System Diseases | |
| Nerve Degeneration | |
| Hypotrichosis | A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles. |
| Mastocytosis | OMIM mapping confirmed by DO. [LS]. |
| Hemolytic-Uremic Syndrome | Xref MGI. |
| Brain Damage, Chronic | |
| Color Vision | |
| Frontotemporal Dementia | A basal ganglia disease characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language. |
| Oligospermia | |
| Night Blindness | |
| Vitelliform Macular Dystrophy | A macular degeneration that can cause progressive vision loss, it is characterized by the disruption of cells in a small area near the center of the retina, the macula. |
| Duodenal Diseases | |
| Cicatrix | |
| Mycoplasma Infections | |
| Child, Gifted | |
| Whiplash Injuries | |
| Myelitis, Transverse | |
| Iatrogenic Disease | |
| Intracranial Hemorrhage, Hypertensive | |
| Tension-Type Headache | A type of headache that last hours with continuous pain of mild or moderate intensity, bilateral location, a pressing/tightening (non-pulsating) quality and that is not aggravated by routine physical activity such as walking or climbing stairs. |
| Photophobia | Excessive sensitivity to light with the sensation of discomfort or pain in the eyes due to exposure to bright light. |
| No-Reflow Phenomenon | |
| Heart Defects, Congenital | |
| Dermatitis, Occupational | |
| Carcinoma, Squamous Cell | |
| Respiratory Tract Diseases | |
| Rectal Neoplasms | |
| Rheumatoid Vasculitis | |
| Cryopyrin-associated Periodic Syndromes | |
| Glioma | A cell type cancer that has_material_basis_in glial cells and is located_in brain or located_in spine. |
| Diabetic Neuropathies | |
| Lymphangioleiomyomatosis | |
| Multiple System Atrophy | OMIM mapping confirmed by DO. [LS]. |
| Sinus Thrombosis, Intracranial | |
| Dupuytren Contracture | An abnormality of the hand resulting from contracture of the palmar fascia with a fixed flexion deformity of the metacarpophalangeal (MCP) joints and the proximal interphalangeal (PIP) joints. |
| 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. |
| 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). |
| Psychotherapy, Group | |
| Proteinuria | |
| Nephritis | |
| Acute Kidney Injury | Sudden loss of renal function, as manifested by decreased urine production, and a rise in serum creatinine or blood urea nitrogen concentration (azotemia). |
| Adrenal Cortex Diseases | |
| Unconsciousness | |
| Mitochondrial Myopathies | |
| Hyperkalemia | An abnormally increased potassium concentration in the blood. |
| Exfoliation Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Pelvic Neoplasms | |
| Funnel Chest | A defect of the chest wall characterized by a depression of the sternum, giving the chest (pectus) a caved-in (excavatum) appearance. |
| Gambling | An activity distinguished primarily by an element of risk in trying to obtain a desired goal, e.g., playing a game of chance for money. |
| Tooth, Nonvital | |
| Intracranial Arteriovenous Malformations | |
| Clostridium Infections | |
| Carpal Tunnel Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Gingival Hemorrhage | |
| Astigmatism | Unequal curvature of the refractive surfaces of the eye. Thus a point source of light cannot be brought to a point focus on the retina but is spread over a more or less diffuse area. This results from the radius of curvature in one plane being longer or shorter than the radius at right angles to it. (Dorland, 27th ed). |
| Balkan Nephropathy | An interstitial nephritis endemic to the regions along the Danube river, in the modern countries of Croatia, Bosnia and Herzegovina, Serbia, Romania and Bulgaria. |
| Actinobacillus Infections | |
| Anxiety, Separation | |
| Takayasu Arteritis | A syndrome that involves inflammation of the aorta that carries blood from the heart to the rest of the body. |
| Muscular Dystrophies | |
| Tuberculosis, Osteoarticular | |
| Foot Ulcer | |
| Galvanic Skin Response | |
| Vulvar Diseases | |
| Dysarthria | Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed. |
| Nephrotic Syndrome | Xref MGI. |
| Bird Fancier's Lung | An extrinsic allergic alveolitis which is caused by inhalation of antigens from avian excreta. The disease has_symptom abrupt onset of dyspnea, has_symptom cough, has_symptom malaise, and has_symptom fever, after exposure to antigen. |
| Interview, Psychological | |
| Ulnar Neuropathies | |
| Choice Behavior | |
| Demyelinating Diseases | |
| Wilms Tumor | |
| Toxoplasmosis, Cerebral | |
| Intervertebral Disc Displacement | |
| Gingival Diseases | |
| Encephalomyelitis, Acute Disseminated | |
| Metaplasia | |
| Isochromosomes | |
| Pelvic Pain | |
| Galactosemias | |
| Median Neuropathy | |
| Vasculitis, Hypersensitivity | |
| Hypopigmentation | A reduction of skin color related to a decrease in melanin production and deposition. |
| Arterial Occlusive Diseases | |
| Neoplasms, Hormone-Dependent | |
| Cognitive Therapy | |
| Arthritis, Reactive | |
| Ventricular Outflow Obstruction | |
| Glycogen Storage Disease | A glycogen metabolism disorder that has_material_basis_in enzymes deficiencies necessary in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types. |
| Theory of Mind | |
| Pouchitis | Acute INFLAMMATION in the INTESTINAL MUCOSA of the continent ileal reservoir (or pouch) in patients who have undergone ILEOSTOMY and restorative proctocolectomy (PROCTOCOLECTOMY, RESTORATIVE). |
| Colonic Polyps | abnormal tissue masses that protrude into the lumen of the colon and are tethered to the wall of the colon |
| Marfan Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Speech Disorders | |
| Adrenal Insufficiency | Insufficient production of steroid hormones (primarily cortisol) by the adrenal glands as a result of a primary defect in the glands themselves. |
| Hernia, Diaphragmatic | |
| Hereditary Autoinflammatory Diseases | |
| Endometritis | |
| Tetralogy of Fallot | OMIM mapping confirmed by DO. [LS]. |
| Pregnancy Complications | |
| Asbestosis | A pneumoconiosis caused by inhalation and retention of asbestos fibers. |
| Stomatitis | |
| Oligomenorrhea | Infrequent menses (less than 6 per year or more than 35 days between cycles). |
| Pyloric Stenosis, Hypertrophic | |
| Attentional Blink | |
| Cerebellar Diseases | |
| Prolactinoma | OMIM mapping confirmed by DO. [SN]. |
| Muscular Dystrophy, Facioscapulohumeral | |
| Scrub Typhus | A typhus that has_material_basis_in Orientia tsutsugamushi, which is transmitted_by trombiculid mites (Leptotrombidium deliense). The infection has_symptom fever, has_symptom headache, has_symptom muscle pain, has_symptom cough, has_symptom maculopapular rash, has_symptom eschar, has_symptom splenomegaly and has_symptom lymphadenopathy. |
| Onychomycosis | A fungal infection of the toenails or fingernails that tends to cause the nails to thicken, discolor, disfigure, and split. |
| Ataxia Telangiectasia | OMIM mapping confirmed by DO. [SN]. |
| von Willebrand Diseases | |
| Hepatoblastoma | |
| Cerebral Arterial Diseases | |
| Factor XIII Deficiency | OMIM mapping confirmed by DO. [SN]. |
| Hearing Loss, Functional | |
| Prostatic Intraepithelial Neoplasia | A neoplastic proliferation of the epithelial cells that line the acini and the ducts of the prostate gland. The neoplastic epithelial cells are confined within the acini and the ducts and they do not invade the surrounding prostatic stroma. Morphologically, it is classified as low or high grade.|noninvasive prostate duct lesions that affect smaller caliber ducts |
| Optic Disk Drusen | |
| Satiety Response | |
| Diffuse Cerebral Sclerosis of Schilder | |
| Aortic Diseases | |
| Wolfram Syndrome | A genetic disease that is characterized by diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding wolframin (WFS1). |
| Edema | An abnormal accumulation of fluid beneath the skin, or in one or more cavities of the body. |
| Nephritis, Interstitial | |
| Lipodystrophy, Familial Partial | |
| Adhesions | |
| Intraoperative Complications | |
| Angioedema | condition similar to urticarai but with swelling occuring in a lower layer of the dermis as well as in the subcutis |
| Asymptomatic Infections | |
| Hypoparathyroidism | A parathyroid gland disease characterized by decreased function of parathyroid glands with underproduction of parathyroid hormone (PTH), leading to abnormally low ionized calcium levels in the blood. |
| Klinefelter Syndrome | No OMIM mapping, confirmed by DO. [LS]. |
| 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. |
| Hyperammonemia | An increased concentration of ammonia in the blood. |
| Hemochromatosis | A metal metabolism disorder characterized by the accumulation of iron in various organs of the body. |
| Osteomalacia | A bone remodeling disease that has_material_basis_in a vitamin D deficiency which results_in softening located_in bone. |
| Leukemia-Lymphoma, T-Cell, Acute, HTLV-I-Associated | |
| Renal Aminoacidurias | |
| Intracranial Embolism and Thrombosis | |
| Achlorhydria | absence of hydrochloric acid in the gastric secretions |
| Leishmaniasis, Mucocutaneous | |
| Motion Sickness | OMIM mapping confirmed by DO. [SN]. |
| Neurofibromatoses | |
| Endometrial Neoplasms | |
| Shoulder Fractures | |
| Ichthyosis, X-Linked | |
| Lynch Syndrome II | |
| Prostatic Diseases | |
| Niemann-Pick Diseases | |
| Huntington Disease | A neurodegenerative disease and an autosomal dominant disease that is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities. |
| Esophageal Atresia | |
| Skin Diseases, Parasitic | |
| Job's Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Holoprosencephaly | A congenital nervous system abnormality characterized by failed or incomplete separation of the forebrain early in gestation; it is accompanied by a spectrum of characteristic craniofacial anomalies. |
| Purpura, Thrombocytopenic | |
| Retention | |
| Leukemia, Biphenotypic, Acute | |
| Hypertrophy | Hypertrophy is the increase in the volume of an organ or tissue due to the enlargement of its component cells. |
| Skull Base Neoplasms | |
| Schizoid Personality Disorder | A personality disorder that is characterized by a lack of interest in social relationships, a tendency towards a solitary lifestyle, secretiveness, emotional coldness and sometimes sexual apathy, with a simultaneous rich, elaborate and exclusively internal fantasy world. |
| Weil Disease | |
| Chylothorax | Accumulation of excessive amounts of lymphatic fluid (chyle) in the pleural cavity. |
| Hyperoxaluria, Primary | |
| Cataract | Partial or complete opacity of the crystalline lens of one or both eyes that decreases visual acuity and eventually results in blindness. Some cataracts appear in infancy or in childhood, but most develop in older individuals. (Sternberg Diagnostic Surgical Pathology, 3rd ed.)|Partial or complete opacity of the crystalline lens of one or both eyes that decreases visual acuity and eventually results in blindness. Some cataracts appear in infancy or in childhood, but most develop in older individuals. (Sternberg Diagnostic Surgical Pathology, 3rd ed.)|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) |
| Adrenal Rest Tumor | |
| Migraine with Aura | A migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon. |
| Ankylosis | Ankylosis is a arthropathy where there is a stiffness of a joint, the result of injury or disease. The rigidity may be complete or partial and may be due to inflammation of the tendinous or muscular structures outside the joint or of the tissues of the joint itself. |
| Myositis Ossificans | A myositis that is accompanied by ossification of muscle tissue or bony deposits in the muscles. |
| Differential Threshold | |
| Pain, Intractable | |
| Fibrosarcoma | |
| Articulation Disorders | |
| Lymphoma, Non-Hodgkin | |
| Gastrointestinal Diseases | |
| Paresis | partial loss of power of voluntary movement in a muscle through injury or disease of it or its nerve supply |
| Intestinal Diseases | |
| Bronchiolitis Obliterans | A obstructive lung disease involving obstruction of the bronchioles due to inflammation and fibrosis which occurs as a complication of various lung conditions or physiological insults. |
| Growth Hormone-Secreting Pituitary Adenoma | OMIM mapping confirmed by DO. [SN]. |
| Temperature Sense | |
| Thyroglossal Cyst | An abnormality of the thyroid gland owing to the presence of a fibrous cyst resulting from the persistence of the thyroglossal duct. |
| Vesico-Ureteral Reflux | A ureteral disease characterized by backward flow of urine from the urinary bladder into the ureter. |
| Pneumoconiosis | An interstitial lung disease that is caused by the inhalation of dust. |
| Carcinoma, Papillary | |
| Respiratory Distress Syndrome, Newborn | |
| Ketosis | Presence of elevated levels of ketone bodies in the body. |
| Lymphoma, Large-Cell, Immunoblastic | |
| Sertoli Cell Tumor | |
| Erythema | Redness of the skin, caused by hyperemia of the capillaries in the lower layers of the skin. |
| Myopia, Degenerative | |
| Carcinoma, Pancreatic Ductal | |
| Cutaneous Fistula | |
| Thromboangiitis Obliterans | OMIM mapping confirmed by DO. [LS]. |
| Brain Ischemia | |
| Lichen Planus, Oral | |
| Muscular Diseases | |
| Mandibulofacial Dysostosis | OMIM mapping confirmed by DO. [SN]. |
| Spinal Muscular Atrophies of Childhood | A spinal muscular atrophy that is associated with the survival of motor neuron protein. |
| Color Vision Defects | |
| Lead Poisoning, Nervous System | |
| Psychophysiology | |
| Dental Pulp Necrosis | |
| Malnutrition | |
| Obsessive-Compulsive Disorder | An anxiety disorder characterized by recurrent, persistent obsessions or compulsions. Obsessions are the intrusive ideas, thoughts, or images that are experienced as senseless or repugnant. Compulsions are repetitive and seemingly purposeful behavior which the individual generally recognizes as senseless and from which the individual does not derive pleasure although it may provide a release from tension. |
| Osteomyelitis | A bone inflammation disease that results_from infection located_in bone and located_in bone marrow. |
| Thecoma | |
| Back Injuries | |
| End Stage Liver Disease | |
| Lung Injury | |
| Airway Remodeling | |
| Epilepsy, Tonic-Clonic | |
| Satiation | |
| Glioblastoma | |
| 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)|A malignant mesenchymal tumor arising from cartilage-forming tissues involving the bones. It affects middle-aged to elderly adults, and the pelvic bones, ribs, shoulder girdle, and long bones are the most common sites of involvement. Most chondrosarcomas arise de novo, but some may develop in a preexisting benign cartilaginous lesion. |
| Lissencephaly | A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation. |
| Branchio-Oto-Renal Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Leukoplakia | |
| Epilepsies, Myoclonic | |
| Gestational Trophoblastic Neoplasms | |
| Anemia, Macrocytic | |
| Warts | Warts, benign growths on the skin or mucous membranes that cause cosmetic problems as well as pain and discomfort. Warts most often occur on the hands, feet, and genital areas. |
| Urticaria | Urticaria is a kind of skin rash notable for pale red, raised, itchy bumps that might also cause a burning or stinging sensation. It is often but not necessarily caused by an allergic reaction. |
| Mental Fatigue | |
| Psychoses, Substance-Induced | |
| Ureaplasma Infections | |
| Stereotypic Movement Disorder | A specific developmental disorder that is characterized by repeated, rhythmic, purposeless movements or activities such as head banging, nail biting, or body rocking. |
| Epilepsy, Post-Traumatic | |
| Intracranial Aneurysm | |
| Fraser Syndrome | |
| Choroidal Neovascularization | new, abnormal, vessel development of the thin, highly vascularized membrane covering most of the posterior of the eye between the retina and the sclera |
| Calcinosis | A calcium metabolism disease that is the result of the formation of calcium deposits in any soft tissue. |
| Spinal Cord Diseases | |
| Fungemia | |
| Thanatophoric Dysplasia | An osteochondrodysplasia that results_in short arms and legs with excess folds of skin. |
| Pregnancy Complications, Neoplastic | |
| Alcohol Withdrawal Seizures | |
| Ichthyosis Vulgaris | OMIM mapping confirmed by DO. [SN]. |
| Hemorrhagic Fever, Crimean | |
| Chronic Periodontitis | |
| Sickle Cell Trait | |
| Biotinidase Deficiency | A multiple carboxylase deficiency that involves a deficiency in biotinidase. |
| Hydatidiform Mole | OMIM mapping confirmed by DO. [SN]. |
| Prostatic Neoplasms | |
| Hypoglycemia | |
| Subacute Sclerosing Panencephalitis | A viral infectious disease that results_in infection located_in brain, has_material_basis_in Measles virus which is immune resistant (which can be a result of a mutation of the virus itself). |
| Hypnosis | |
| Premenstrual Syndrome | |
| Arrhythmias, Cardiac | |
| Leukemia, Plasma Cell | |
| Legg-Perthes Disease | Avascular necrosis of the proximal epiphysis of the femur occurring in growing children and caused by an interruption of the blood supply to the head of the femur close to the hip joint. The necrosis is characteristically associated with flattening of the femoral head, for which reason the term coxa plana has been used to refer to this feature in the medical literature. |
| Carney Complex | An autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity. |
| Arteriosclerosis Obliterans | |
| Optic Atrophy, Hereditary, Leber | |
| Canavan Disease | OMIM mapping confirmed by DO. [SN]. |
| Hermanski-Pudlak Syndrome | |
| Gastroparesis | |
| Congenital Disorders of Glycosylation | |
| Arthritis, Juvenile Rheumatoid | |
| Upper Extremity Deformities, Congenital | |
| Mental Retardation, X-Linked | |
| Disseminated Intravascular Coagulation | |
| Thoracic Injuries | |
| Stroop Test | |
| HIV Infections | |
| Paraganglioma | Xref MGI. |
| Bone Demineralization, Pathologic | |
| REM Sleep Behavior Disorder | A sleep disorder that involves abnormal behavior including the acting out of violent or dramatic dreams during the sleep phase with rapid eye movement. |
| Persistent Vegetative State | |
| Complex Regional Pain Syndromes | |
| Dysplastic Nevus Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Auditory Perceptual Disorders | |
| Giant Lymph Node Hyperplasia | |
| Hyperthyroidism | A thyroid gland disease that involves an over production of thyroid hormone. |
| Carcinoma, Neuroendocrine | |
| Neuroma, Acoustic | |
| Jaw Abnormalities | any structural anomaly of the bony framework of the mouth where the teeth are held |
| Insulinoma | A benign tumor of the PANCREATIC BETA CELLS. Insulinoma secretes excess INSULIN resulting in HYPOGLYCEMIA.|A usually benign, well circumscribed neoplasm arising from the beta cells of the pancreas. Patients exhibit symptoms related to hypoglycemia due to inappropriate secretion of insulin. |
| Lipid Metabolism Disorders | |
| Leukocyte Disorders | |
| Heart Neoplasms | |
| Leg Ulcer | |
| Volition | |
| Ependymoma | The presence of an ependymoma of the central nervous system. |
| 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)|A malignant, usually aggressive tumor composed of atypical, neoplastic melanocytes. Most often, melanomas arise in the skin (cutaneous melanomas) and include the following histologic subtypes: superficial spreading melanoma, nodular melanoma, acral lentiginous melanoma, and lentigo maligna melanoma. Cutaneous melanomas may arise from acquired or congenital melanocytic or dysplastic nevi. Melanomas may also arise in other anatomic sites including the gastrointestinal system, eye, urinary tract, and reproductive system. Melanomas frequently metastasize to lymph nodes, liver, lungs, and brain. |
| Mucocele | |
| Lead Poisoning, Nervous System, Childhood | |
| Chorea | A movement disease characterized by brief, semi-directed, irregular movements that not repetitive or rhythmic, but appear to flow from one muscle to the next. |
| Bronchial Hyperreactivity | A chronic respiratory disease manifested as difficulty breathing due to the narrowing of bronchial passageways.|Tendency of the smooth muscle of the tracheobronchial tree to contract more intensely in response to a given stimulus than it does in the response seen in normal individuals. This condition is present in virtually all symptomatic patients with asthma. The most prominent manifestation of this smooth muscle contraction is a decrease in airway caliber that can be readily measured in the pulmonary function laboratory.|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).|A bronchial disease that is characterized by chronic inflammation and narrowing of the airways, which is caused by a combination of environmental and genetic factors resulting in recurring periods of wheezing (a whistling sound while breathing), chest tightness, shortness of breath, mucus production and coughing. The symptoms appear due to a variety of triggers such as allergens, irritants, respiratory infections, weather changes, excercise, stress, reflux disease, medications, foods and emotional anxiety. |
| Optic Atrophy, Autosomal Dominant | |
| Chondrocalcinosis | An arthritis that has_material_basis_in the accumulation of salt crystals located_in joint. |
| Peripheral Vascular Diseases | |
| Depressive Disorder, Major | |
| Thrombocythemia, Essential | |
| Low Tension Glaucoma | |
| Achondroplasia | An osteochondrodysplasia that results_in dwarfism which has_material_basis_in abnormal ossification of cartilage in located_in long bone. |
| Gastric Outlet Obstruction | |
| Small Cell Lung Carcinoma | 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)|A highly aggressive subtype of lung carcinoma characterized by the presence of malignant small cells and necrosis. Metastatic disease is usually present at the time of diagnosis.|A highly aggressive subtype of lung carcinoma characterized by the presence of malignant small cells and necrosis. Metastatic disease is usually present at the time of diagnosis. (NCI05) |
| Ileal Neoplasms | |
| Xeroderma Pigmentosum | An autosomal recessive disease that is characterized by a deficiency in the ability to repair ultraviolet damage that has_material_basis_in autosomal recessive inheritance of DNA repair. |
| Gastroenteritis | A gastrointestinal system infectious disease that involves inflammation of the lining of the stomach and small and large intestines, which is caused by viruses, bacteria, or parasites. Chemicals and drugs also cause gastroenteritis. The symptoms include diarrhea, loss of appetite, nausea, vomiting, cramps, and discomfort in the abdomen. |
| Acute Chest Syndrome | A lung disease that involves a vasoocclusive crisis of the pulmonary vasculature seen in patients with sickle cell anemia. The crisis is initiated by a lung infection, and the resulting inflammation and loss of oxygen tension leads to sickling of red cells and further vasoocclusion. The disease has_symptom fever, has_symptom pleuritic chest pain, has_symptom tachypnea, has_symptom cough, has_symptom hypoxemia, has_symptom marked leukocytosis, and has_symptom diffuse infiltrates on chest radiograph. |
| Rosacea | |
| Vulvitis | |
| Hypolipoproteinemias | |
| Cystadenocarcinoma | An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, in which cystic accumulations of retained secretions are formed. |
| Anorexia Nervosa | An eating disorder characterized by refusal to maintain a healthy body weight, and an obsessive fear of gaining weight due to a distorted self image. |
| Mycobacterium avium-intracellulare Infection | |
| Myopathies, Structural, Congenital | |
| Central Nervous System Diseases | |
| Tendinopathy | |
| Death, Sudden, Cardiac | |
| Spondylolisthesis | A bone structure disease that has_material_basis_in displacement located_in set of vertebrae. |
| Heart Septal Defects | |
| Li-Fraumeni Syndrome | An autosomal dominant disease characterized by increases risk of developing several types of cancer, including breast cancer, osteosarcomata and soft tissue sarcomata. |
| Biliary Tract Neoplasms | |
| Melioidosis | A primary bacterial infectious disease that results_in infection, has_material_basis_in Burkholderia pseudomallei, which is transmitted_by contact with the contaminated water or soil. The infection has_symptom fever, has_symptom respiratory distress, has_symptom chest pain, and has_symptom stomach pain. |
| Keloid | A tough heaped-up scar that rises quite abruptly above the rest of the skin. It is irregularly shaped and tends to enlarge progressively. Keloids arise when there is too much collagen formed in the dermis during the repair of connective tissue. |
| Shock, Septic | |
| Meditation | |
| Antisocial Personality Disorder | A personality disorder that involves a pervasive pattern of disregard for, and violation of, the rights of others that begins in childhood or early adolescence and continues into adulthood. |
| Neoplastic Processes | |
| Micrognathism | |
| Manifest Anxiety Scale | |
| Retinitis Pigmentosa | A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. |
| Chromosome Disorders | |
| Motor Skills Disorders | |
| Osteitis Deformans | A bone formation disease that has_material_basis_in hyperactive osteoclast which results_in abnormal osteoblast bone formation located_in skull, located_in pelvis, located_in vertebral column, located_in set of limbs. |
| Nervous System Diseases | |
| HELLP Syndrome | A severe pre-eclampsia characterized by hemolysis, elevated liver enzyme and low platelet count. |
| Silicosis | A pneumoconiosis that is an inflammation and scarring of the uper lobes of the lungs causing nodular lesions resulting from inhalation of silica, quartz or slate particles. |
| Pancreatic Pseudocyst | Cyst-like space not lined by epithelium and contained within the pancreas. Pancreatic pseudocysts are often associated with pancreatitis. |
| Pemphigoid, Benign Mucous Membrane | |
| Trypanosomiasis, African | |
| Attention Deficit and Disruptive Behavior Disorders | |
| Oral Ulcer | A stomatitis characterized by the repeated formation of benign and non-contagious mouth ulcers. |
| Disease Models, Animal | |
| Abdominal Pain | An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) and perceived to originate in the abdomen. |
| Multiple Sclerosis | A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring. |
| Sleep Bruxism | |
| Obstetric Labor, Premature | |
| Choristoma | |
| Drug Eruptions | |
| Pelvic Inflammatory Disease | |
| Brain Hemorrhage, Traumatic | |
| Hepatitis, Viral, Human | INFLAMMATION of the LIVER in humans due to infection by VIRUSES. There are several significant types of human viral hepatitis with infection caused by enteric-transmission ( HEPATITIS A; HEPATITIS E) or blood transfusion ( HEPATITIS B; HEPATITIS C; and HEPATITIS D). |
| Schistosomiasis japonica | A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia. |
| Sleep, REM | |
| Autonomic Nervous System Diseases | |
| Anovulation | |
| Bezoars | |
| Knee Injuries | |
| Fractures, Bone | Breaks in bones. |
| Phenylketonurias | |
| Moraxellaceae Infections | |
| Hyperventilation | Hyperventilation refers to an increased pulmonary ventilation rate that is faster than necessary for the exchange of gases. Hyperventilation can result from increased frequency of breathing, an increased tidal volume, or both, and leads to an excess intake of oxygen and the blowing off of carbon dioxide. |
| Sick Building Syndrome | An extrinsic allergic alveolitis that is characterized by a set of symptoms such as headache, fatigue, eye irritation, and breathing difficulties that affect workers in modern airtight office buildings. The disease is caused by indoor pollutants (as formaldehyde fumes, particulate matter, or microorganisms), and the symptoms tend to disappear when affected individuals leave the building. |
| Pancreatitis, Acute Necrotizing | |
| Sebaceous Gland Diseases | |
| Sciatica | Pain in the lower back and hip radiating in the distribution of the sciatic nerve. |
| Lead Poisoning | |
| Menopause, Premature | |
| Optic Nerve Diseases | |
| Substance Withdrawal Syndrome | A substance-specific organic brain syndrome that follows the discontinuation of administration or use, or reduction in intake of an addictive substance, e.g. opioids, barbiturates and alcohol; amphetamines or similarly acting sympathomimetics; cocaine; nicotine; sedatives, hypnotics, or anxiolytics. Syndrome manifests with diverse, often painful physical and psychological symptoms, which include but not limited to intense drug craving, anxiety, depression, insomnia, nausea, perspiration, body aches, tremors, hallucinations, and convulsions. |
| Tooth Mobility | |
| Escherichia coli Infections | |
| Intestinal Polyposis | The presence of multiple polyps in the intestine. |
| Hematoma | |
| Activated Protein C Resistance | Poor anticoagulant response to activated protein C. A plasma is termed 'APC resistant' when the addition of exogenous APC fails to prolong its clotting time in an activated partial thromboplastin time assay. |
| Motor Neuron Disease | A neurodegenerative disease that is located_in the motor neurones. |
| Paracoccidioidomycosis | A primary systemic mycosis that results_in systemic fungal infection located_in mucosa, located_in lymph nodes, located_in bone, located_in skin or located_in lungs, has_material_basis_in Paracoccidioides brasiliensis. |
| Psoriasis | A common genetically determined, chronic, inflammatory skin disease characterized by rounded erythematous, dry, scaling patches. The lesions have a predilection for nails, scalp, genitalia, extensor surfaces, and the lumbosacral region. Accelerated epidermopoiesis is considered to be the fundamental pathologic feature in psoriasis. |
| Lymphatic Metastasis | |
| Bacteriuria | A urinary system disease which consists of the presence of bacteria in urine. |
| Parasitemia | A disease by infectious agent that is carried out by a parasite which by definition is a pathogen that simultaneously injures and derives sustenance from its host. |
| Breast Diseases | |
| Gastritis, Atrophic | |
| Amyloidosis, Familial | |
| Hypertension, Pregnancy-Induced | |
| Schizotypal Personality Disorder | A personality disorder that involves a need for social isolation, anxiety in social situations, odd behavior and thinking, and often unconventional beliefs. |
| Esophageal Neoplasms | |
| Adenocarcinoma, Follicular | |
| Maze Learning | |
| Hemoglobinuria, Paroxysmal | |
| Parathyroid Neoplasms | |
| Bone Diseases | |
| Adenocarcinoma, Bronchiolo-Alveolar | |
| Urinary Incontinence, Urge | |
| Cadmium Poisoning | |
| Guillain-Barre Syndrome | An autoimmune disease of peripheral nervous system that causes body's immune system to attack part of the peripheral nervous system. |
| Brain Diseases | |
| Bone Resorption | The process in which specialized cells known as osteoclasts degrade the organic and inorganic portions of bone, and endocytose and transport the degradation products. |
| Leukemia, Radiation-Induced | |
| Pleasure | |
| Obesity | An eating-related disorder in which excess body fat has accumulated to such an extent that health may be negatively affected. It is commonly defined as a body mass index (weight divided by height squared) of 30 kg/m2 or higher.|A status with BODY WEIGHT that is grossly above the acceptable or desirable weight, 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). |
| Leukemia, Experimental | |
| Vertebral Artery Dissection | |
| Hemianopsia | Partial or complete loss of vision in one half of the visual field of one or both eyes. |
| Stomatitis, Herpetic | |
| Urinary Bladder, Overactive | |
| Retinal Drusen | OMIM mapping confirmed by DO. [SN]. |
| Leukemia, B-Cell | |
| Liposarcoma | A malignant lipomatous neoplasm that arises in fat cells in deep soft tissue retroperitoneum.|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)|A usually painless malignant tumor that arises from adipose tissue. Microscopically, it may contain a spectrum of neoplastic adipocytes ranging from lipoblasts to pleomorphic malignant adipocytes. Representative morphologic variants include: well differentiated, dedifferentiated, pleomorphic, and myxoid/round cell liposarcoma. The metastatic potential is higher in less differentiated tumors. |
| Iron Overload | |
| Lymphomatoid Granulomatosis | |
| Pericardial Effusion | A pericardium disease that is characterized by an abnormal accumulation of fluid in the pericardial cavity. |
| Factor XII Deficiency | OMIM mapping confirmed by DO. [SN]. |
| Mucositis | |
| Hypertension, Renovascular | |
| Leukemia, Myelomonocytic, Chronic | |
| Retroperitoneal Neoplasms | |
| Manganese Poisoning | |
| Muscle Cramp | |
| Soft Tissue Injuries | |
| Amino Acid Metabolism, Inborn Errors | |
| Coronary Vessel Anomalies | |
| Bulimia | A form of anomalous eating behavior characterized by binge eating is followed by self-induced vomiting or other compensatory behavior intended to prevent weight gain (purging, fasting or exercising or a combination of these). |
| Cellulitis | |
| Recognition | |
| Sunburn | An injury to the skin causing erythema, tenderness, and sometimes blistering and resulting from excessive exposure to the sun. The reaction is produced by the ultraviolet radiation in sunlight. |
| Aphakia | absence of the crystalline lens of the eye |
| Fibromuscular Dysplasia | |
| Memory Disorders | |
| Varicose Veins | A vein disease that is characterized by swollen, twisted veins visible just under the surface of the skin. |
| Fibrous Dysplasia, Polyostotic | |
| XYY Karyotype | |
| Darier Disease | |
| Osteophyte | A hyperostosis that involves formation of new bone on the surface of preexisting bone. |
| Adrenoleukodystrophy | A leukodystrophy that disrupts the breakdown of very-long-chain fatty acids resulting in progressive brain damage, failure of the adrenal glands and eventually death. |
| Foramen Ovale, Patent | |
| Ventricular Dysfunction, Left | |
| Carcinoma, Adenosquamous | |
| Postphlebitic Syndrome | A venous insufficiency that is characterized by aching pain, heaviness, swelling, cramps, itching, or tingling in the affected limb and is a chronic complication of deep venous thrombosis. |
| Endometriosis | The growth of functional endometrial tissue in anatomic sites outside the uterine body. It most often occurs in the pelvic organs. |
| Aortic Aneurysm | An aortic disease that is characterized by an enlargement (dilation) of the aorta to greater than 1.5 times normal size. |
| Chromosome Breakage | A type of chromosomal aberration characterized by an increased susceptibility to chromosomal breakage induced by treatment of cultured lymphocytes with agents such as chemical mutagens, irradiation, and alkylating agents. |
| Alzheimer Disease | A dementia that results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting in late middle age and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid. It is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability.|A progressive, neurodegenerative disease characterized by loss of function and death of nerve cells in several areas of the brain leading to loss of cognitive function such as memory and language.|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)|A dementia which is an incurable disease of unknown cause, starting in late middle age or in old age, that results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood, that leads in advanced cases to a profound decline in cognitive and physical functioning, and that is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid. |
| Leishmaniasis, Cutaneous | |
| Neoplasms | |
| Rectal Fistula | The presence of a fistula affecting the rectum. |
| Peutz-Jeghers Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Kernicterus | |
| Retinal Vasculitis | |
| Eczema | A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin. |
| Epilepsies, Partial | |
| Dihydropyrimidine Dehydrogenase Deficiency | A purine-pyrimidine metabolic disorder that is an autosomal recessive metabolic disorder in which there is absent or significantly decreased activity of dihydropyrimidine dehydrogenase, an enzyme involved in the metabolism of uracil and thymine. |
| Intestinal Pseudo-Obstruction | |
| Syndrome | A disease comprised of a group of signs and symptoms that occur together and characterize a particular abnormality. |
| Kidney Neoplasms | Tumors or cancers of the KIDNEY. |
| Blood Coagulation Disorders | |
| Leukemia, Megakaryoblastic, Acute | |
| Fetal Death | |
| Enterovirus Infections | |
| Diurnal Enuresis | |
| Hemangioma, Capillary | |
| Malocclusion | Dental malocclusion refers to an abnormality of the occlusion, or alignment, of the teeth and the way the upper and lower teeth fit together, resulting in overcrowding of teeth or in abnormal bite patterns. |
| Gonadoblastoma | A cell type benign neoplasm that is composed_of a mixture of gonadal elements. |
| Spondylarthritis | |
| Root Resorption | |
| Leprosy, Multibacillary | |
| Neoplasms, Bone Tissue | |
| Leber Congenital Amaurosis | A retinal disease that is characterized by nystagmus, sluggish or no pupillary responses, and severe vision loss or blindness. |
| Cystic Fibrosis | An autosomal recessive disease that is characterized by the buildup of thick, sticky mucus that can damage many organs. |
| Blindness | |
| Scotoma | |
| Dominance, Cerebral | |
| Spinal Osteophytosis | |
| Constriction, Pathologic | |
| Autoimmune Diseases | |
| Paralysis, Hyperkalemic Periodic | |
| Schizophrenia, Disorganized | |
| Blood Platelet Disorders | |
| Thrombocythemia, Hemorrhagic | |
| Leukemia, Lymphoid | |
| Craniofacial Abnormalities | any structural anomaly of the face or head affecting appearance |
| Beckwith-Wiedemann Syndrome | A syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations. |
| Onchocerciasis | A filariasis that involves parasitic infection caused by the nematode Onchocerca volvulus, which is transmitted to humans through the bite of a blackfly of the genus Simulium. The worms spread throughout the body and, when they die, cause intense itching and a strong immune system response that can destroy nearby tissue. The symptoms include pruritus, dermatitis, blindness, onchocercomata (subcutaneous nodules), and lymphadenopathy. |
| Mitochondrial Encephalomyopathies | |
| Stomatitis, Aphthous | |
| Polyneuropathies | |
| Disease Progression | |
| Hearing Loss, Sensorineural | |
| Acute Lung Injury | Acute lung injury (ALI) is a diffuse heterogeneous lung injury characterized by hypoxemia, non cardiogenic pulmonary edema, low lung compliance and widespread capillary leakage. ALI is caused by any stimulus of local or systemic inflammation, principally sepsis. |
| Thyroiditis | Updating to more specific UMLS_CUI from C0029495 to C0040147. |
| Urinary Tract Infections | |
| Fibrous Dysplasia of Bone | An autosomal dominant disease that involves skin pigmentation, bone and hormonal problems along with premature puberty. It is caused by mutations in the GNAS1 gene. |
| Disease Susceptibility | |
| Thyroid Hormone Resistance Syndrome | OMIM mapping confirmed by DO. [LS]. |
| Rett Syndrome | A pervasive developmental disease that is a neurological and developmental disorder that mostly occurs in females and is caused_by a mutation on the MECP2 gene on the X chromosome. Infants with Rett syndrome seem to grow and develop normally at first, but then stop developing and even lose skills and abilities. |
| Nondisjunction, Genetic | |
| Tenosynovitis | |
| Lymphoma, T-Cell, Peripheral | |
| MMPI | |
| Lower Extremity Deformities, Congenital | |
| 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).|A disease of the heart muscle or myocardium proper. Cardiomyopathies may be classified as either primary or secondary, on the basis of etiology, or on the pathophysiology of the lesion: hypertrophic, dilated, or restrictive. |
| Adenocarcinoma | A type of carcinoma derived from glandular tissue or in which tumor cells form recognizable glandular structures.|A malignant epithelial tumor with a glandular organization. |
| Delayed Graft Function | |
| Leukemia, B-Cell, Chronic | |
| Pneumonia, Mycoplasma | |
| Colitis, Ulcerative | |
| Abetalipoproteinemia | A hypolipoproteinemia that is characterized by an inablility to fully absorb dietary fats, cholesterol and fat-soluble vitamins, has_physical_basis_in an autosomal recessive disorder of lipid metabolism caused by mutation of the microsomal triglyceride transfer protein that catalyzes the transport of lipids (TRIGLYCERIDES; CHOLESTEROL ESTERS; PHOSPHOLIPIDS) and is required in the secretion of BETA-LIPOPROTEINS (low density lipoproteins or LDL). |
| Confusion | Lack of clarity and coherence of thought, perception, understanding, or action. |
| Dysautonomia, Familial | |
| Candidiasis | An opportunistic mycosis that involves fungal infection of the mouth, throat, skin, scalp, vagina, fingers, nails, bronchi, lungs, heart and brain by Candida species, of which Candida albicans is the most common. Systemic Candida infections are usually confined to severely immunocompromised persons. |
| Diseases in Twins | |
| Hypertension, Malignant | |
| Echinococcosis, Hepatic | |
| Retinal Neovascularization | formation of new blood vessels originating from the retinal veins and extending along the inner (vitreal) surface of the retina |
| Cachexia | Severe weight loss, wasting of muscle, loss of appetite, and general debility related to a chronic disease. |
| Humeral Fractures | |
| 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). |
| Aphasia, Primary Progressive | |
| Fibromyalgia | A chronic disorder of unknown etiology characterized by pain, stiffness, and tenderness in the muscles of neck, shoulders, back, hips, arms, and legs. Other signs and symptoms include headaches, fatigue, sleep disturbances, and painful menstruation. |
| Choreatic Disorders | |
| Peritoneal Neoplasms | |
| Fetal Alcohol Syndrome | A fetal alcohol spectrum disorder that results in severe mental and physical defects which can develop in a child when the mother drinks alcohol during pregnancy. The presenting features include craniofacial dysmorphology (microcephaly, smooth philtrum, thin upper lip, small eye openings), pre- and postnatal growth deficiency, and central nervous system dysfunction. |
| Glomus Jugulare Tumor | |
| Hemorrhagic Fever with Renal Syndrome | A viral infectious disease that is a hemorrhagic fever, located_in kidney, has_material_basis_in Hantaan virus, has_material_basis_in Dobrava-Belgrade virus, has_material_basis_in Seoul virus, or has_material_basis_in Puumala virus, which are carried and transmitted_by rodents. The infection has_symptom headache, has_symptom fever, has_symptom muscle pains, has_symptom facial flush, has_symptom petechiae, has_symptom hemorrhagic features, has_symptom proteinuria, and has_symptom renal failure. |
| Amyloidosis | An acquired metabolic disease that involves abnormal deposited of amyloid proteins in organs and/or tissues. |
| Lewy Body Disease | A dementia and a synucleinopathy that is characterized by the development of abnormal proteinaceous (alpha-synuclein) cytoplasmic inclusions, called Lewy bodies, throughout the brain that results in progressive decline in mental abilities. |
| Glucose Metabolism Disorders | |
| Corneal Diseases | |
| Ocular Motility Disorders | |
| Hyperlipoproteinemia Type IV | OMIM mapping confirmed by DO. [SN]. |
| Cervical Intraepithelial Neoplasia | |
| Campylobacter Infections | |
| Hyperlipoproteinemia Type II | |
| Prion Diseases | |
| Tuberculosis, Gastrointestinal | |
| Myositis | An inflammatory process affecting the skeletal muscles. Causes include infections, injuries, and autoimmune disorders.|Inflammation of a muscle or muscle tissue. |
| Esophageal and Gastric Varices | |
| Pneumonia, Pneumococcal | |
| Kashin-Beck Disease | |
| Conjunctivitis | Conjunctivitis is a conjunctival disease described as a inflammation of the conjunctiva, the outermost layer of the eye and the inner surface of the eyelids, which is most commonly due to an allergic reaction or an infection (usually viral, but sometimes bacterial. Fungal infections are rare and occur mainly in people who use corticosteroid eye drops for a long time or have eye injuries involving vegetable matter. Newborns are particularly susceptible to eye infections, which they acquire from organisms in the mother's birth canal (neonatal conjunctivitis. |
| Brain Injuries | |
| Epidermolysis Bullosa Acquisita | |
| Periodontitis | Inflammation and loss of connective tissues supporting or surrounding the teeth. This may involve any part of the PERIODONTIUM. Periodontitis is currently classified by disease progression (CHRONIC PERIODONTITIS; AGGRESSIVE PERIODONTITIS) instead of age of onset. (From 1999 International Workshop for a Classification of Periodontal Diseases and Conditions, American Academy of Periodontology) |
| Fluorosis, Dental | |
| Death, Sudden | |
| Cardiovascular Diseases | |
| Genomic Instability | abnormalities of DNA metabolism, DNA repair, cell-cycle governance, or control of apoptosis that increase the probability that whole chromosomes or pieces of chromosomes are gained or lost during cell division, resulting in an imbalance in the number of chromosomes per cell (aneuploidy) and an enhanced rate of loss of heterozygosity |
| Lung Diseases, Fungal | |
| Diverticulitis | |
| Impotence, Vasculogenic | |
| Short Bowel Syndrome | |
| Delirium, Dementia, Amnestic, Cognitive Disorders | |
| Fetal Diseases | |
| Liver Failure | |
| Diabetes Insipidus, Nephrogenic | |
| Bone Neoplasms | |
| Sarcoidosis, Pulmonary | |
| Friedreich Ataxia | Xref MGI. |
| Aptitude | |
| Impulse Control Disorders | |
| Arthritis, Rheumatoid | |
| Systemic Inflammatory Response Syndrome | |
| Chagas Cardiomyopathy | a form of cardiomyopathy that develops as a result of Chagas disease, an infection with the protozoan parasite Trypanosoma Cruzi |
| Mobility Limitation | |
| Elephantiasis | |
| Pituitary Diseases | |
| Acromegaly | A disease of metabolism that has_material_basis_in excessive growth hormone production which results_in enlargement located_in limb. |
| Headache Disorders, Secondary | |
| Leukodystrophy, Metachromatic | |
| Fractures, Closed | |
| Rubella | A viral infectious disease that results_in infection located_in skin, has_material_basis_in Rubella virus, which is transmitted_by droplet spread of oronasal secretions from the infected person through coughing and sneezing, and transmitted_by congenital method. The infection has_symptom rash on the face which spreads to the trunk and limbs, has_symptom fever, has_symptom lymphadenopathy, has_symptom joint pains, has_symptom headache, and has_symptom conjunctivitis. |
| Tachycardia, Sinus | |
| Chickenpox | A viral infectious disease that results_in infection located_in skin, has_material_basis_in Human herpesvirus 3, which is transmitted_by direct contact with secretions from the rash, or transmitted_by droplet spread of respiratory secretions. The infection has_symptom anorexia, has_symptom myalgia, has_symptom nausea, has_symptom fever, has_symptom headache, has_symptom sore throat, and has_symptom blisters. |
| Hallucinations | Perceptions in a conscious and awake state in the absence of external stimuli which have qualities of real perception, in that they are vivid, substantial, and located in external objective space. |
| Hypertriglyceridemia | A condition of elevated levels of TRIGLYCERIDES in the blood. |
| Colitis, Microscopic | |
| Tuberculosis | A primary bacterial infectious disease that is located_in lungs, located_in lymph nodes, located_in pericardium, located_in brain, located_in pleura or located_in gastrointestinal tract, has_material_basis_in Mycobacterium tuberculosis, which is transmitted_by droplets released into the air when an infected person coughs or sneezes. |
| Upper Extremity Deep Vein Thrombosis | |
| Tachycardia, Supraventricular | |
| Leigh Disease | A mitochondrial metabolism disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity. |
| Hypogonadism | A gonadal disease that is characterized by diminished functional activity of the gonads. |
| Typhoid Fever | A primary bacterial infectious disease that is a communicable systemic illness, has_material_basis_in Salmonella enterica subsp enterica serovar Typhi, which is transmitted_by ingestion of food or water contaminated with the feces of an infected person. The infection has_symptom fever, has_symptom diarrhea, has_symptom prostration, has_symptom headache, has_symptom splenomegaly, has_symptom liver enlargement, has_symptom eruption of rose-colored spots, and has_symptom leukopenia. |
| Turner Syndrome | No OMIM mapping, confirmed by DO. [LS]. |
| 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)|An intraneural or extraneural neoplasm arising from nerve tissues and neural sheaths. It is composed of perineurial-like fibroblasts and Schwann cells. It usually presents as a localized cutaneous lesion and less often as a circumscribed peripheral nerve mass. Patients with neurofibromatosis type 1 present with multiple masses. Neurofibromas which arise from major nerves and plexiform neurofibromas are precursor lesions to malignant peripheral nerve sheath tumors.|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 (MeSH). |
| Dengue | |
| Obesity, Morbid | |
| Cerebellar Ataxia | A cerebellar disease characterized by ataxia originating in the cerebellum. |
| Leukemia, Large Granular Lymphocytic | |
| Carcinoma, Endometrioid | |
| Werner Syndrome | OMIM mapping confirmed by DO. [LS]. |
| Mental Health | The state wherein the person is well adjusted. |
| Anomia | An agnosia that involves a severe problem with recalling words or names. |
| Consciousness | |
| Gastrointestinal Hemorrhage | Hemorrhage affecting the gastrointestinal tract. |
| Femur Head Necrosis | |
| Ascorbic Acid Deficiency | |
| Dehydration | |
| Carcinoma, Intraductal, Noninfiltrating | |
| Hyperhomocysteinemia | An amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood. |
| Muscular Atrophy, Spinal | |
| Herpes Simplex | A viral infectious disease that results_in_formation_of lesions, located_in mouth, located_in face, located_in genitalia, or located_in hands, has_material_basis_in Human herpesvirus 1 or has_material_basis_in Human herpesvirus 2, which are transmitted_by direct contact with an active lesion or body fluid of an infected person. |
| Counseling | |
| Uveal Neoplasms | |
| Migraine Disorders | |
| Idiopathic Pulmonary Fibrosis | Chronic and progressive fibrosis of the lung parenchyma of unknown cause. |
| Protein-Energy Malnutrition | |
| Geriatric Psychiatry | |
| Histiocytoma, Malignant Fibrous | |
| Melanoma, Amelanotic | |
| Tachycardia, Ventricular | |
| Diarrhea | A gastrointestinal system disease described as the condition of having frequent loose or liquid bowel movements. Acute diarrhea is a common cause of death in developing countries and the second most common cause of infant deaths worldwide. The loss of fluids through diarrhea can cause severe dehydration which is one cause of death in diarrhea sufferers. Along with water, sufferers also lose dangerous amounts of important salts, electrolytes, and other nutrients. There are at least four types of diarrhea: secretory diarrhea, osmotic diarrhea, motility-related diarrhea, and inflammatory diarrhea. |
| Pulmonary Alveolar Proteinosis | A lung disease that is characterized by abnormal accumulation of surfactant occurs within the alveoli, interfering with gas exchange. |
| Aortic Rupture | |
| Sensation Disorders | |
| Polymyositis | |
| Pigmentation Disorders | |
| Thyroiditis, Autoimmune | |
| Central Nervous System Neoplasms | |
| Thoracic Neoplasms | |
| Lipidoses | |
| Peritoneal Diseases | |
| Hyperparathyroidism | A parathyroid gland disease characterized by an overactivity of the parathyroid glands, leading to an excess of parathyroid hormone in the body. |
| Xanthomatosis, Cerebrotendinous | |
| Cleidocranial Dysplasia | An osteochondrodysplasia that has_material_basis_in mutations in the RUNX2 gene which results_in undeveloped or absent located_in clavicle along with delayed closing of fontanels in the located_in skull. |
| Spinal Stenosis | A bone deterioration disease that has_material_basis_in bony spurs, disc degeneration, or thickened ligaments which results_in narrowing located_in spinal cord. |
| Ganglioglioma | |
| Phyllodes Tumor | A benign, borderline, or malignant fibroepithelial neoplasm arising from the breast and rarely the prostate gland. It may recur following resection. The recurrence rates are higher for borderline and malignant phyllodes tumors. In borderline and malignant phyllodes tumors metastases to distant anatomic sites can occur. The incidence of metastases is higher in malignant phyllodes tumors.|A type of connective tissue neoplasm arising from intralobular stroma of the BREAST. It is characterized by the rapid enlargement of an asymmetric firm mobile mass. Histologically, its leaf-like stromal clefts are lined by EPITHELIAL CELLS.|A type of connective tissue neoplasm typically arising from intralobular stroma of the breast. It is characterized by the rapid enlargement of an asymmetric firm mobile mass. Histologically, its leaf-like stromal clefts are lined by EPITHELIAL CELLS. Rare phyllodes tumor of the prostate is also known. |
| Hernia, Inguinal | |
| Prostatism | |
| Carcinoma, Renal Cell | |
| 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)|Increased pressure in the eyeball due to obstruction of the outflow of aqueous humor. |
| Malaria, Vivax | |
| Child Psychology | |
| Test Anxiety Scale | |
| Pica | An appetite for and the persistent ingestion of non-food substances such as clay. In order to diagnose pica, this behavior must have persisted over a period of at least one month. |
| Sleep Stages | |
| Coronary Vasospasm | |
| Lupus Erythematosus, Cutaneous | |
| Muscle Rigidity | Continuous involuntary sustained muscle contraction. When an affected muscle is passively stretched, the degree of resistance remains constant regardless of the rate at which the muscle is stretched. This feature helps to distinguish rigidity from muscle spasticity. |
| Taste | |
| Intervertebral Disk Degeneration | |
| Epilepsy, Temporal Lobe | |
| Cardiovascular Abnormalities | |
| Surgical Wound Infection | |
| Cholelithiasis | Presence or formation of GALLSTONES in the BILIARY TRACT, usually in the gallbladder (CHOLECYSTOLITHIASIS) or the common bile duct (CHOLEDOCHOLITHIASIS). |
| Denys-Drash Syndrome | An autosomal dominant disease that is characterized by the association of diffuse mesangial sclerosis (DMS), male pseudohermaphroditism with a 46,XY karyotype, and nephroblastoma that derives_from an abnormality in the WT1 gene (Wilms' tumor suppressor gene). |
| Stevens-Johnson Syndrome | |
| Hypercapnia | Abnormally elevated blood carbon dioxide (CO2) level. |
| Abscess | |
| Deltaretrovirus Infections | |
| Carotid Body Tumor | |
| Spondylarthropathies | |
| Vascular Diseases | |
| Infertility, Male | |
| Urologic Diseases | |
| Body Weight | The mass or quantity of heaviness of an individual. It is expressed by units of pounds or kilograms. |
| Mouth, Edentulous | |
| Skin Diseases, Vesiculobullous | |
| Stomach Neoplasms | |
| Leprosy, Paucibacillary | |
| Antiphospholipid Syndrome | A hypersensitivity reaction type II disease that is characterized by recurrent venous or arterial thrombosis and/or fetal losses associated with characteristic elevated levels of antibodies directed against membrane anionic phospholipids (anticardiolipin). |
| Reinforcement | |
| Connective Tissue Diseases | |
| Osteoporosis, Postmenopausal | Metabolic disorder associated with fractures of the femoral neck, vertebrae, and distal forearm. It occurs commonly in women within 15-20 years after menopause, and is caused by factors associated with menopause including estrogen deficiency. |
| Granuloma, Pyogenic | |
| Forensic Psychiatry | |
| Mouth Abnormalities | any structural anomaly of the oral cavity |
| Genetic Diseases, Inborn | |
| Lung Diseases | |
| Pregnancy Complications, Cardiovascular | |
| Ulna Fractures | Fractures of the larger bone of the forearm. |
| Anterior Wall Myocardial Infarction | |
| Out-of-Hospital Cardiac Arrest | |
| Viremia | An infection that has as part virus particles located in the blood. |
| Postpartum Thyroiditis | |
| 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)|A malignant, invasive embryonal neoplasm arising from the cerebellum. It occurs predominantly in children and has the tendency to metastasize via the cerebrospinal fluid pathways. Signs and symptoms include truncal ataxia, disturbed gait, lethargy, headache, and vomiting. There are four histologic variants: classic medulloblastoma, desmoplastic medulloblastoma, large cell medulloblastoma, and medulloblastoma with extensive nodularity and advanced neuronal differentiation. (from NCI Thesuarus) |
| Hepatitis D | A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis delta virus, which is an incomplete virus that requires the helper function of Hepatitis B virus to replicate and only occurs among people who are infected with the Hepatitis B virus. The infection has_symptom fatigue, has_symptom lethargy, has_symptom anorexia, has_symptom nausea, has_symptom jaundice, has_symptom clay-colored stools, has_symptom dark urine, has_symptom changes in personality, has_symptom disturbances in sleep, has_symptom confusion, has_symptom abnormal behavior, has_symptom somnolence, and has_symptom coma. |
| Hepatitis E | A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis E virus, which is transmitted_by ingestion of contaminated food. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom dark urine, has_symptom joint pain, and has_symptom jaundice. |
| Giardiasis | A parasitic protozoa infectious disease that involves infection of the small intestine by a single-celled enteric protozoan parasite Giardia intestinalis. The symptoms include greasy and malodorous stools, diarrhea, abdominal pain, bloating, nausea, and vomiting. |
| Lymphoma, Large B-Cell, Diffuse | |
| Hepatitis A | A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis A virus, which is transmitted_by ingestion of contaminated food or water, or transmitted_by direct contact with an infected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice. |
| Hepatitis B | A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis B virus, which is transmitted_by sexual contact, transmitted_by blood transfusions, and transmitted_by fomites like needles or syringes. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice. |
| Hepatitis C | A viral infectious disease that results_in inflammation located_in liver, has_material_basis_in Hepatitis C virus, which is transmitted_by blood from an infected person enters the body of an uninfected person. The infection has_symptom fever, has_symptom fatigue, has_symptom loss of appetite, has_symptom nausea, has_symptom vomiting, has_symptom abdominal pain, has_symptom clay-colored bowel movements, has_symptom joint pain, and has_symptom jaundice. |
| Severe Combined Immunodeficiency | A combined T cell and B cell immunodeficiency that is caused by a defect in several genes encoding for B and T lymphocytes resulting in individuals with non-functional immune systems. |
| Starvation | |
| Inflammatory Breast Neoplasms | |
| Facies | |
| Telangiectasia, Hereditary Hemorrhagic | |
| Respiratory Syncytial Virus Infections | |
| Spherocytosis, Hereditary | |
| Osteoarthritis, Spine | |
| Stroke | An artery disease that is characterized by dysfunction of the blood vessels supplying the brain. |
| Trauma, Nervous System | |
| Agricultural Workers' Diseases | |
| Colorectal Neoplasms, Hereditary Nonpolyposis | |
| Primary Graft Dysfunction | |
| Lymphoproliferative Disorders | |
| Sjogren's Syndrome | A hypersensitivity reaction type II disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. |
| Vasospasm, Intracranial | |
| Joint Diseases | |
| Neoplasm, Residual | |
| Neuroectodermal Tumors, Primitive | |
| Genital Diseases, Male | |
| Hypospadias | A physical disorder characterized by an abnormally placed urethral opening on the underside of the penis or on the perineum. |
| Parasitic Diseases | |
| Anemia, Hypochromic | |
| Apnea | Lack of breathing with no movement of the respiratory muscles and no exchange of air in the lungs. This term refers to a disposition to have recurrent episodes of apnea rather than to a single event. |
| Sweat Gland Diseases | |
| Leukemia, Myeloid, Acute | |
| Social Perception | |
| Myocardial Infarction | Xref MGI. |
| Nervous System Malformations | |
| Fibroadenoma | A breast benign neoplasm comprised of fibrous and glandoular tissues located_in breast. |
| Hypokinesia | Abnormally diminished motor activity. In contrast to paralysis, hypokinesia is not characterized by a lack of motor strength, but rather by a poverty of movement. The typical habitual movements (e.g., folding the arms, crossing the legs) are reduced in frequency. |
| Cardiomyopathy, Hypertrophic | |
| Hashimoto Disease | |
| Nuchal Cord | A complication of pregnancy and delivery in which the umbilical cord wraps around the fetal neck once or multiple times. |
| Ureteral Neoplasms | |
| Erysipelas | |
| Protein C Deficiency | |
| Leukemia, B-Cell, Acute | |
| Weight Loss | Reduction inexisting body weight. |
| Intracranial Embolism | |
| Pneumonia, Pneumocystis | |
| Vulvar Lichen Sclerosus | |
| Leukemia, Myelocytic, 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. |
| Hydrocephalus, Normal Pressure | |
| Cryoglobulinemia | A condition characterized by the presence of cryoglobulins in the blood. Cryoglobulins are abnormal proteins that precipitate within the microvasculature on exposure to cold; microvasculature effects of cryoglobulinemia may result in restricted tissue blood flow, tissue hypoxia, and tissue necrosis. --2004 |
| Granulomatous Disease, Chronic | |
| Hepatitis, Alcoholic | |
| Dissociative Disorders | |
| Endometrial Hyperplasia | overdevelopment or increased size, usually due an increased number of cells, of the glandular mucous membrane lining of the uterine cavity that is hormonally responsive during the estrous/menstrual cycle and during pregnancy |
| Skin Diseases, Vascular | |
| Puerperal Disorders | |
| Esophagitis, Peptic | |
| Torsades de Pointes | A type of ventricular tachycardia characterized by polymorphioc QRS complexes that change in amplitue and cycle length, and thus have the appearance of oscillating around the baseline in the EKG. |
| Optic Atrophy | Xref MGI. |
| Learning | Any process in an organism in which a relatively long-lasting adaptive behavioral change occurs as the result of experience. |
| Eating Disorders | |
| Gynecomastia | |
| Ovarian Failure, Premature | |
| DNA Virus Infections | |
| Carcinoma, Lobular | |
| Atrial Flutter | A type of atrial arrhythmia characterized by atrial rates of between 240 and 400 beats per minute and some degree of atrioventricular node conduction block. Typically, the ventricular rate is half the atrial rate. In the EKG; atrial flutter waves are observed as sawtooth-like atrial activity. Pathophysiologically, atrial flutter is a form of atrial reentry in which there is a premature electrical impulse creates a self-propagating circuit. |
| Neoplasms, Neuroepithelial | |
| Appendicitis | A gastrointestinal system infectious disease that involves inflammation and infection of the appendix caused by the blockage of the lumen with a small, hard piece of stool, a foreign body or worms. Mucus backs up in the appendiceal lumen, causing bacteria that live inside the appendix to multiply. The infection has_symptom pain, in the upper abdomen initially and later in the lower abdomen, has_symptom nausea, has_symptom vomiting and has_symptom fever. |
| Leukemia, Neutrophilic, Chronic | |
| Gangrene | A serious and potentially life-threatening condition that arises when a considerable mass of body tissue dies (necrosis). |
| Glomerulonephritis | A nephritis that causes inflammation of the glomeruli located_in kidney. |
| Auditory Perception | |
| Gender Identity | |
| Paraneoplastic Polyneuropathy | |
| Leiomyomatosis | |
| Thrombocytosis | A myeloma and blood platelet disease that is characterized by the presence of high platelet counts in the blood. |
| Common Bile Duct Neoplasms | |
| Colonic Neoplasms | |
| Carcinoma, Medullary | |
| Microcephaly | OMIM mapping confirmed by DO. [SN]. |
| Granuloma, Lethal Midline | |
| Attention Deficit Disorder with Hyperactivity | |
| Channelopathies | |
| Sexually Transmitted Diseases | |
| Peritonitis | A gastrointestinal system disease that involves inflammation of the peritoneum resulting from perforation of the gastrointestinal tract, which produces immediate chemical inflammation followed shortly by infection from intestinal organisms. Peritonitis can also result from appendicitis, diverticulitis, strangulating intestinal obstruction, pancreatitis, pelvic inflammatory disease, mesenteric ischemia, intraperitoneal blood, barium, or peritoneo-systemic shunts, drains, and dialysis catheters in the peritoneal cavity. The symptoms include abdominal pain and tenderness, fever, fluid in the abdomen, nausea, vomiting and low urine output. |
| Sexual Dysfunction, Physiological | |
| Urination Disorders | |
| Postpartum Hemorrhage | Significant maternal haemorrhage/blood loss following deilvery of a child. |
| Desmoplastic Small Round Cell Tumor | Desmoplastic small round cell tumor (DSRCT) is an aggressive soft tissue cancer that typically arises in serous lined surfaces of the abdominal or pelvic peritoneum, and spreads to the omentum, lymph nodes and hematogenously disseminates especially to the liver. Extraserous primary location has been reported in exceptional cases. |
| Candidiasis, Invasive | |
| Encephalitis, Herpes Simplex | |
| Adenomatous Polyps | |
| Psychomotor Disorders | |
| Carcinoma, Hepatocellular | |
| Taste Perception | |
| Hypertension, Renal | |
| Erythema Nodosum | An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral. |
| Personality Disorders | |
| Hearing Loss, Mixed Conductive-Sensorineural | |
| Leukemia, Pre-B-Cell | |
| Water Intoxication | |
| Epilepsy, Benign Neonatal | |
| Asthenozoospermia | loss or reduction of the mobility of the spermatozoa, frequently associated with infertility |
| Acquired Hyperostosis Syndrome | |
| Periodontitis, Juvenile | |
| 22q11 Deletion Syndrome | A chromosomal disease that has_material_basis_in deletion polymorphisms at chromosome location 22q11 and is characterized by variable developmental problems and schizoid features. |
| Retinoblastoma | A retinal cell cancer and malignant neoplasm of retina and neuroblastoma and neuroendocrine tumors that derives_from the tissues of the retina. |
| Takayasu's Arteritis | A syndrome that involves inflammation of the aorta that carries blood from the heart to the rest of the body. |
| Uveoparotid Fever | |
| Cerebral Palsy | A brain disease that is caused by damage to the motor control centers of the developing brain during pregnancy, during childbirth or after birth, which affects muscle movement and balance. |
| Glycosuria | An increased concentration of glucose in the urine. |
| Burkholderia Infections | |
| Neurodermatitis | |
| Neoplastic Cells, Circulating | |
| Ichthyosis | An abnormality of the skin characterized the presence of excessive amounts of dry surface scales on the skin resulting from an abnormality of keratinization. |
| Hyperparathyroidism, Primary | |
| Opportunistic Infections | |
| Hypergammaglobulinemia | An increased level of gamma globulin (immunoglobulin) in the blood. |
| Muscular Atrophy | |
| Adenoma, Villous | |
| Coma | Complete absence of wakefulness and content of conscience, which manifests itself as a lack of response to any kind of external stimuli. |
| 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. |
| Hepatitis, Toxic | A spectrum of clinical liver diseases ranging from mild biochemical abnormalities to ACUTE LIVER FAILURE, caused by drugs, drug metabolites, and chemicals from the environment. |
| Genetic Diseases, Y-Linked | |
| Colorectal Neoplasms | uncontrolled cell growth (neoplasia) occurring in the colon, rectum or vermiform appendix. |
| Choroid Diseases | |
| Infantile Apparent Life-Threatening Event | |
| Shock | |
| Cluster Headache | A type of headache characterized by repeated attacks of unilateral pain lasting 15 to 180 minutes and associated with local autonomic signs. |
| Pneumonia | A lung disease that involves lung parenchyma or alveolar inflammation and abnormal alveolar filling with fluid (consolidation and exudation). It results from a variety of causes including infection with bacteria, viruses, fungi or parasites, and chemical or physical injury to the lungs. It is accompanied by fever, chills, cough, and difficulty in breathing. |
| Nephrosis | |
| Pseudoxanthoma Elasticum | An autosomal recessive disease characterized by the accumulation of deposits of calcium and other minerals in elastic fibers, which are a component of connective tissue, this can result in changes in the skin, eyes, cardiovascular system and gastrointestinal system. |
| Metal Metabolism, Inborn Errors | |
| Visual Perception | The series of events required for an organism to receive a visual stimulus, convert it to a molecular signal, and recognize and characterize the signal. Visual stimuli are detected in the form of photons and are processed to form an image. |
| Cataplexy | A sudden and transient episode of bilateral loss of muscle tone, often triggered by emotions. |
| Leukomalacia, Periventricular | |
| Fetofetal Transfusion | |
| Deafness | A decreased magnitude of the sensory perception of sound. |
| Elephantiasis, Filarial | |
| Nose Neoplasms | |
| Fibrocystic Breast Disease | |
| Hearing Loss, Bilateral | |
| Uterine Cervical Diseases | |
| Respiratory Insufficiency | Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide. |
| Niemann-Pick Disease, Type C | OMIM mapping confirmed by DO. [SN]. |
| Neck Pain | |
| Arteriosclerosis | An artery disease that is characterized by a thickening and hardening of arterial walls in the arteries. |
| Rhabdoid Tumor | Rhabdoid tumor (RT) is an aggressive pediatric soft tissue sarcoma that arises in the kidney, the liver, the peripheral nerves and all miscellaneous soft-parts throughout the body. RT involving the central nervous system (CNS) is called atypical teratoid rhabdoid tumor (ATRT; see this term). |
| Vestibulocochlear Nerve Diseases | |
| Recurrence | |
| Ciliary Motility Disorders | |
| Psychological Tests | |
| Memory | The activities involved in the mental information processing system that receives (registers), modifies, stores, and retrieves informational stimuli. The main stages involved in the formation and retrieval of memory are encoding (processing of received information by acquisition), storage (building a permanent record of received information as a result of consolidation) and retrieval (calling back the stored information and use it in a suitable way to execute a given task). |
| Pneumonia, Viral | |
| Liver Cirrhosis, Biliary | |
| Dwarfism | A severe degree of short stature, more than -4 SD from the mean corrected for age and sex. |
| 46, XX Disorders of Sex Development | |
| Hearing Loss, Noise-Induced | |
| Atrioventricular Block | A heart conduction disease that is characterized by the impairment of the conduction between the atria and ventricles of the heart. |
| Goiter | Enlargement of the THYROID GLAND that may increase from about 20 grams to hundreds of grams in human adults. Goiter is observed in individuals with normal thyroid function (euthyroidism), thyroid deficiency ( HYPOTHYROIDISM), or hormone overproduction ( HYPERTHYROIDISM). Goiter may be congenital or acquired, sporadic or endemic ( GOITER, ENDEMIC). |
| Myelitis | |
| Otitis Media with Effusion | |
| Amphetamine-Related Disorders | |
| Gram-Negative Bacterial Infections | |
| Bacteroidaceae Infections | |
| Lymphoma, Follicular | |
| Geographic Atrophy | |
| Achievement | |
| Anemia | A reduction in the number of circulating erythrocytes or in the quantity of hemoglobin. |
| Multiple Chemical Sensitivity | A syndrome that is an adverse physical reaction to low levels of many common chemicals. |
| Leukemia, Lymphocytic, Chronic, B-Cell | |
| Andersen Syndrome | A long QY syndrome that has_material_basis_in autosomal dominant inheritance of a mutation in the KCNJ2 gene which disrupts the rhythm of the heart's lower chambers (ventricular arrhythmia) and results_in an unusually small lower jaw (micrognathia), low-set ears, and an abnormal curvature of the fingers called clinodactyly. |
| Hyperkeratosis, Epidermolytic | |
| Hypopharyngeal Neoplasms | |
| Rhinitis, Allergic, Seasonal | |
| Hyperbilirubinemia, Neonatal | |
| Carcinoma, Large Cell | |
| Pneumococcal Infections | Infections with bacteria of the species STREPTOCOCCUS PNEUMONIAE. |
| Digestive System Abnormalities | any structural anomaly of the system dedicated to the mechanical, chemical, and enzymatic processing of food |
| Wrist Injuries | |
| Gout | Hereditary 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. |
| Platybasia | A developmental malformation of the occipital bone and upper end of the cervical spine, in which the latter appears to have pushed the floor of the occipital bone upward such that there is an abnormal flattening of the skull base. |
| Diabetic Foot | |
| Erythroblastosis, Fetal | |
| Language Tests | |
| Hypertelorism | Interpupillary distance more than 2 SD above the mean (alternatively, the appearance of an increased interpupillary distance or widely spaced eyes). |
| Port-Wine Stain | A congenital vascular malformation consisting of superficial and deep dilated capillaries in the skin which produce a reddish to purplish discolouration of the skin. |
| Gingivitis | |
| Gait Disorders, Neurologic | |
| Prehypertension | |
| Keratoconus | A corneal disease characterized by structural changes within the cornea causing it to thin and change, leading to a protruding conical shape. |
| Carcinoma, Basal Cell | |
| Felty's Syndrome | A syndrome that results_in rheumatoid arthritis, splenomegaly and neutropenia. |
| Neuropsychology | |
| Acidosis | Abnormal acid accumulation or depletion of base. |
| Hyperostosis | A bone remodeling disease that results in an abnormal growth of located_in bone. |
| Altitude Sickness | |
| Perceptual Masking | |
| Xerophthalmia | |
| Anoxemia | |
| Varicose Ulcer | |
| Glomerulonephritis, IGA | |
| Papillomavirus Infections | |
| Rupture | |
| Peanut Hypersensitivity | |
| Stress | |
| Biliary Tract Diseases | |
| Cognition | Intellectual or mental process whereby an organism becomes aware of or obtains knowledge. |
| Skin Diseases, Bacterial | |
| Borderline Personality Disorder | A personality disorder that involves a prolonged disturbance of personality function characterized by depth and variability of moods. |
| Poisoning | |
| Diarrhea, Infantile | |
| Brucellosis | A primary bacterial infectious disease that is caused by the bacteria of the genus Brucella, when humans come in contact with contaminated animals or animal products or ingestion of infected food products. The disease has_symptom fever, has_symptom sweat, has_symptom headache, has_symptom back pain, has_symptom physical weakness, has_symptom joint pain and has_symptom fatigue. |
| Yellow Fever | A viral infectious disease that results_in infection, has_material_basis_in Yellow fever virus, which is transmitted_by Aedes, transmitted_by Haemagogus, or transmitted_by Sabethes species of mosquitoes. The infection has_symptom fever, has_symptom muscle pain, has_symptom backache, has_symptom headache, has_symptom shivers, has_symptom loss of appetite, has_symptom jaundice, and has_symptom bleeding from the mouth, nose, eyes or stomach leading to vomitus containing blood. |
| Fanconi Syndrome | A renal tubular transport disease of the proximal renal tubes characterized by glucosuria, phosphaturia, generalized aminoaciduria and HCO3 wasting. |
| Embolism | |
| Sensory Deprivation | |
| Malocclusion, Angle Class II | |
| Endodermal Sinus Tumor | A germ cell cancer that has_material_basis_in cells that line the yolk sac of the embryo. |
| Ascites | Accumulation of serous fluid in the spaces between tissues and organs in the cavity of the abdomen. |
| Bronchiolitis, Viral | |
| Meningitis, Pneumococcal | |
| Renal Insufficiency, Chronic | |
| Cholangiocarcinoma | |
| Penile Neoplasms | |
| Paresthesia | Abnormal sensations such as tingling, pricking, or numbness of the skin with no apparent physical cause. |
| Leprosy, Lepromatous | |
| Adie Syndrome | A syndrome that is a neurological disorder affecting the pupil of the eye and the autonomic nervous system. It is characterized by one eye with a pupil that is larger than normal and constricts slowly in bright light (tonic pupil), along with the absence of deep tendon reflexes, usually in the Achilles tendon. |
| Mumps | A viral infectious disease that results_in inflammation located_in salivary gland, has_material_basis_in Mumps virus, which is transmitted_by droplet spread of saliva or mucus from the mouth, nose, or throat of an infected person, or transmitted_by contaminated fomites. The infection has_symptom fever, has_symptom headache, has_symptom muscle aches, has_symptom tiredness, has_symptom loss of appetite, has_symptom swollen and tender salivary glands under the ears or jaw on one or both sides of the face. |
| Entamoebiasis | A parasitic protozoa infectious disease that involves infection caused by the amoeba Entamoeba histolytica. Amebic invasion of the intestinal lining causes dysentery, colitis or diarrhea. The infection can also spread through the blood to the liver and, rarely, to the lungs, brain or other organs. |
| Hepatitis, Chronic | |
| Alkalosis | Depletion of acid or accumulation base in the body fluids. |
| HIV Seropositivity | |
| Leukemia, Myelomonocytic, Juvenile | |
| Headache | Cephalgia, or pain sensed in various parts of the head, not confined to the area of distribution of any nerve. |
| Community Mental Health Services | |
| Maxillary Sinusitis | A sinusitis which involves infection of maxillary sinuses that causes pain or pressure over the cheeks just below the eyes, tooth ache, and headache. |
| Leukemia, Megakaryocytic, Acute | |
| Eosinophilic Esophagitis | An esophagitis characterized by inflammation involving eosinophils located_in esophagus. |
| Dilatation, Pathologic | |
| Gingival Overgrowth | |
| Precursor B-Cell Lymphoblastic Leukemia-Lymphoma | |
| Staphylococcal Skin Infections | |
| Herpes Labialis | |
| Chromosome Aberrations | |
| Pregnancy, Ectopic | |
| Hydronephrosis | |
| Electroshock | |
| Kidney Diseases, Cystic | |
| Heart Septal Defects, Atrial | |
| Skin Diseases, Metabolic | |
| Neoplastic Syndromes, Hereditary | |
| Alopecia Areata | A hypersensitivity reaction type II disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. |
| Sensory Thresholds | |
| Perceptual Disorders | |
| Urolithiasis | presence of calculi in any part of the urinary system |
| Bradycardia | A slower than normal heart rate (in adults, slower than 60 beats per minute). |
| Ventricular Dysfunction, Right | |
| Sexually Transmitted Diseases, Viral | |
| Uveitis, Intermediate | |
| Keratosis | |
| Papilloma | A cell type benign neoplam that is composed_of epithelial tissue on papillae of vascularized connective tissue. |
| Liver Diseases | |
| Caliciviridae Infections | |
| Blast Crisis | |
| Hemangioma, Cavernous, Central Nervous System | |
| Time Perception | |
| Myotonic Dystrophy | |
| Paramyxoviridae Infections | |
| Translocation, Genetic | |
| Cockayne Syndrome | An autosomal recessive disease that is caused by rare mutations in two DNA excision repair proteins, ERCC-8 and ERCC-6, and characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging. |
| Optic Neuropathy, Ischemic | |
| Anencephaly | |
| Skull Fractures | |
| Decision Making | |
| Aortic Stenosis, Supravalvular | |
| Auditory Threshold | |
| Enterocolitis, Necrotizing | |
| Breast Neoplasms | |
| Myoma | |
| Mental Retardation | |
| Spinal Injuries | |
| Odontogenic Cysts | |
| HTLV-I Infections | |
| Pseudomonas Infections | Infections with bacteria of the genus PSEUDOMONAS. |
| Costello Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Hand Deformities, Congenital | |
| Hepatic Vein Thrombosis | |
| Hyperaldosteronism | An adrenal gland hyperfunction disease that results in the overproduction of aldosterone by the adrenal glands. |
| Osteolysis | Osteolysis refers to the destruction of bone through bone resorption with removal or loss of calcium. |
| Blushing | |
| Cerebral Amyloid Angiopathy | An amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes that usually result in spontaneous cerebral hemorrhage, ischemic lesions and progressive dementia. |
| Uterine Cervical Incompetence | |
| Lymphocytosis | Increase in the number or proportion of lymphocytes in the blood. |
| Pulmonary Edema | |
| Reward | |
| Intestinal Atresia | |
| Binge-Eating Disorder | |
| Mouth Neoplasms | |
| Hypocalcemia | An abnormally decreased calcium concentration in the blood. |
| Systemic Vasculitis | |
| Retinal Neoplasms | |
| Heartburn | |
| Aortic Valve Stenosis | An aortic valve disease that has_physical_basis_in incomplete opening of the aortic valve. |
| Convalescence | |
| Space Perception | |
| Basal Ganglia Hemorrhage | |
| Leukemia, Lymphocytic, Acute, L1 | |
| Discrimination | |
| Cryptococcosis | An opportunistic mycosis that results_in fungal infection and has_material_basis_in Cryptococcus neoformans or Cryptococcus gattii. |
| Cecal Neoplasms | |
| Corneal Opacity | A reduction of corneal clarity. |
| Anorexia | A lack or loss of appetite for food (as a medical condition). |
| Asphyxia | |
| Hepatorenal Syndrome | |
| Limb Deformities, Congenital | |
| Liver Neoplasms, Experimental | |
| Jejunal Neoplasms | |
| Charcot-Marie-Tooth Disease | |
| Sex Cord-Gonadal Stromal Tumors | |
| Avoidance Learning | |
| Radius Fractures | |
| Radiculopathy | |
| Psychotic Disorders | |
| Heat Stroke | |
| Malformations of Cortical Development | |
| Alagille Syndrome | A liver disease that is characterized by an accumulation of bile in the liver resulting from a reducted number of liver small bile ducts. |
| Placenta Diseases | |
| Thyrotoxicosis | A thyroid gland disease that is characterized by excess thyroid hormone. |
| Haemophilus Infections | |
| Breast Neoplasms, Male | |
| Speech Perception | The process whereby an utterance is decoded into a representation in terms of linguistic units (sequences of phonetic segments which combine to form lexical and grammatical morphemes). |
| Neoplasms, Multiple Primary | |
| Spina Bifida Cystica | |
| Oligodendroglioma | A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). (Adapted from WHO.)|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)|A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). (Adapted from WHO)|A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). (Adapted from WHO.)|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 (MeSH).|A well-differentiated (WHO grade II), diffusely infiltrating neuroglial tumor of adults, typically located in the cerebral hemispheres. It is composed predominantly of cells which morphologically resemble oligodendroglia. The neoplastic cells have rounded homogeneous nuclei and, on paraffin sections, a swollen, clear cytoplasm ('honeycomb' appearance). It generally recurs locally, with median post-operative survival times ranging from 3 to 5 years for patients with all histological grades. (Adapted from WHO.) |
| Paget Disease, Extramammary | |
| Myocardial Ischemia | Thickening and loss of elasticity of the CORONARY ARTERIES, leading to progressive arterial insufficiency (CORONARY DISEASE).|Pathological processes of CORONARY ARTERIES that may derive from a congenital abnormality, atherosclerotic, or non-atherosclerotic cause.|Narrowing of the coronary arteries due to fatty deposits inside the arterial walls.|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. |
| Cholangitis, Sclerosing | |
| Heredodegenerative Disorders, Nervous System | |
| Carcinoma, Transitional Cell | |
| Alcohol Amnestic Disorder | |
| Acquired Immunodeficiency Syndrome | A Human immunodeficiency virus infectious disease that results_in reduction in the numbers of CD4-bearing helper T cells below 200 per µL of blood or 14% of all lymphocytes thereby rendering the subject highly vulnerable to life-threatening infections and cancers, has_material_basis_in Human immunodeficiency virus 1 or has_material_basis_in Human immunodeficiency virus 2, which are transmitted_by sexual contact, transmitted_by transfer of blood, semen, vaginal fluid, pre-ejaculate, or breast milk, transmitted_by congenital method, and transmitted_by contaminated needles. Opportunistic infections are common in people with AIDS. |
| Sarcoma, Synovial | |
| Neuroendocrine Tumors | |
| Glomus Tumor | A hemangiopericytic tumor that is a mesenchymal neoplasm composed of cells that closely resemble the modified smooth muscle cells of the normal glomus body. |
| Horse Diseases | |
| Adenocarcinoma, Clear Cell | |
| Myopia | A refractive error in which rays of light entering the EYE parallel to the optic axis are brought to a focus in front of the RETINA when accommodation (ACCOMMODATION, OCULAR) is relaxed. This results from an overly curved CORNEA or from the eyeball being too long from front to back. It is also called nearsightedness. |
| Eye Infections, Fungal | |
| Disease | A disease is a disposition that describes states of disease associated with a particular sample and/or organism. |
| Porphyrias | |
| Hearing Loss, High-Frequency | |
| Peripheral Arterial Disease | |
| Thyroid Dysgenesis | |
| Homocystinuria | An amino acid metabolic disorder that involves an accumulation of homocysteine in the serum and an increased excretion of homocysteine in the urine. |
| Leukoaraiosis | An abnormality of the cerebral white matter. |
| Communication Disorders | |
| Constipation | |
| Choledochal Cyst | |
| Albinism, Ocular | |
| Mevalonate Kinase Deficiency | OMIM mapping confirmed by DO. [SN]. |
| Lymphoma, Large-Cell, Anaplastic | |
| Vaginal Neoplasms | |
| Cholecystitis | A cholangitis that is an inflammation of the gallbladder. |
| Hemolysis | |
| Spinal Diseases | |
| Nephrogenic Fibrosing Dermopathy | Nephrogenic systemic fibrosis (NSF) is a rare systemic fibrosing condition observed in renally impaired patients and characterized by a hardening and thickening of the skin with fibrotic plaques or papules, pruritus, joint pain and stiffness, muscle weakness, limitation of range of motion, and yellowed eyes. It is generally associated with administration of gadolinium-based magnetic resonance imaging contrast agents (GBCA) in patients with kidney disease. |
| Protoporphyria, Erythropoietic | |
| Immune Complex Diseases | |
| Salivary Gland Diseases | |
| Kyphosis | Exaggerated anterior convexity of the thoracic vertebral column. |
| Leukemia, T-Cell, Acute | |
| Glomerulonephritis, Membranous | |
| Tongue Neoplasms | |
| Glycogen Storage Disease Type III | |
| Craniofacial Dysostosis | A craniosynostosis that involves premature fusion of certain skull bones. This early fusion prevents the skull from growing normally and affects the shape of the head and face. The disease is associated with mutations in the FGFR2 gene. |
| Epilepsy, Complex Partial | |
| Angioid Streaks | OMIM mapping confirmed by DO. [SN]. |
| Carcinoma, Papillary, Follicular | |
| Egg Hypersensitivity | |
| Lymphoma, Lymphoblastic | |
| Leukemia, Lymphocytic, Acute, L2 | |
| Supratentorial Neoplasms | |
| Periodontal Attachment Loss | |
| Ornithine Carbamoyltransferase Deficiency Disease | |
| Psychoacoustics | |
| Lymphoma, T-Cell | |
| Penile Induration | |
| Asthenia | |
| Adenocarcinoma, Papillary | |
| Orthostatic Intolerance | |
| Shock, Cardiogenic | |
| Still's Disease, Adult-Onset | |
| Depressive Disorder | A condition characterized by pervasive dysphoric mood, loss of interests, and inability to experience pleasure. |
| Leukemia, Myelogenous, Chronic, BCR-ABL Positive | |
| Loeys-Dietz Syndrome | |
| Foot Deformities, Congenital | |
| Fascioliasis | A parasitic helminthiasis infectious disease that involves parasitic infection of the bile ducts of the liver by Fasciola hepatica or Fasciola gigantica. During the acute phase, manifestations include abdominal pain, hepatomegaly, fever, vomiting, diarrhea, urticaria and eosinophilia. Occasionally, infection occurs in intestinal wall, lungs, subcutaneous tissue, and pharyngeal mucosa. |
| Craniocerebral Trauma | |
| Spastic Paraplegia, Hereditary | |
| Lyme Disease | A primary bacterial infectious disease that results_in infection, has_material_basis_in Borrelia burgdorferi, which is transmitted_by blacklegged tick (Ixodes scapularis) or transmitted_by western blacklegged tick (Ixodes pacificus). The infection has_symptom fever, has_symptom headache, has_symptom fatigue, and has_symptom skin rash called erythema migrans. If left untreated, infection can spread to joints, the heart, and the nervous system. |
| Choroid Plexus Neoplasms | |
| Infarction, Anterior Cerebral Artery | |
| Orbital Diseases | |
| Dystonia | |
| Purpura, Schoenlein-Henoch | |
| Idiopathic Interstitial Pneumonias | |
| Cytochrome-c Oxidase Deficiency | |
| Dental Calculus | |
| Neurogenic Inflammation | |
| Color Perception | |
| Cardiomyopathy, Dilated | |
| Hippel-Lindau Disease | |
| 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. The three most prominent theories used to explain the etiology of the disease are that acids produced by bacteria lead to decalcification; that micro-organisms destroy the enamel protein; or that keratolytic micro-organisms produce chelates that lead to decalcification. |
| Thalamic Diseases | |
| Uveitis, Anterior | |
| Arthrogryposis | Persistent flexure or contracture of a joint. (Dorland, 27th ed) |
| Myoclonic Epilepsy, Juvenile | |
| Uterine Cervical Neoplasms | |
| IgG Deficiency | An abnormally decreased level of immunoglobulin IgG in blood. |
| Hypoalphalipoproteinemias | |
| Polyendocrinopathies, Autoimmune | |
| Myxoma | |
| Hemorrhagic Disease of Newborn | |
| Colonic Diseases, Functional | |
| Macrophage Activation Syndrome | |
| Pharyngeal Diseases | |
| Xanthomatosis | A lipid storage disease that is characterized by the desposition of yellowish cholesterol-rich material in tendons or other body parts. |
| Neutropenia | |
| Endocrine Gland Neoplasms | |
| Microscopic Polyangiitis | Microscopic polyangiitis (MPA) is an inflammatory, necrotizing, systemic vasculitis that affects predominantly small vessels (i.e. small arteries, arterioles, capillaries, venules) in multiple organs. |
| Uremia | |
| Gigantism | |
| Personal Construct Theory | |
| Sexual Dysfunctions, Psychological | |
| Mesothelioma | A usually malignant and aggressive neoplasm of the mesothelium which is often associated with exposure to asbestos.|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) |
| Neoplasms, Complex and Mixed | |
| Malocclusion, Angle Class I | |
| Uterine Neoplasms | |
| Hearing Loss, Sudden | |
| Pneumonia, Ventilator-Associated | |
| Venous Insufficiency | A vein disease that is characterized by impaired flow of blood through the veins. |
| Pituitary Neoplasms | |
| Male Urogenital Diseases | |
| Spinal Fractures | Broken bones in the vertebral column. |
| 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.|A condition of diminution or cessation of secretion of one or more hormones from the anterior pituitary gland. This may result from surgical or radiation ablation, non-secretory pituitary neoplasms, metastatic tumors, infarction, pituitary apoplexy, infiltrative or granulomatous processes, and other conditions. |
| Rupture, Spontaneous | |
| Myasthenia Gravis | OMIM mapping confirmed by DO. [SN]. |
| TDP-43 Proteinopathies | |
| Eosinophilia | |
| Factor XI Deficiency | OMIM mapping confirmed by DO. [SN]. |
| Vitamin B Deficiency | |
| Polycystic Kidney Diseases | |
| Glomerulonephritis, Membranoproliferative | |
| Colles' Fracture | |
| Lymphoma, Large-Cell | |
| Scalp Dermatoses | |
| Retinal Perforations | |
| Fallopian Tube Neoplasms | |
| Cyclothymic Disorder | A bipolar disorder that involves recurrent hypomanic and dysthymic episodes, but no full manic episodes or full major depressive episodes. |
| 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)|A malignant smooth muscle cancer that can arise almost anywhere in the body, but is most common in the uterus, abdomen, or pelvis.|An uncommon, aggressive malignant smooth muscle neoplasm, usually occurring in post-menopausal women. It is characterized by a proliferation of neoplastic spindle cells. Morphologic variants include epithelioid, granular cell, inflammatory and myxoid leimyosarcomas. |
| Aggressive Periodontitis | A periodontitis that is characterized by rapid attachment loss and bone destruction in the presence of little local factors such as dental plaque and dental calculus resulting in inflammation and a loss of periodontium. |
| Cues | |
| Conditioning, Operant | |
| Tic Disorders | |
| Musculoskeletal Abnormalities | |
| Intussusception | OMIM mapping confirmed by DO. [SN]. |
| Leptospirosis | A primary bacterial infectious disease that involves systemic infection, has_material_basis_in Leptospira, which is transmitted_by contact with water, food, or soil containing urine from the infected animals. The infection has_symptom jaundice, has_symptom chills, has_symptom fever, has_symptom muscle pain, and has_symptom hepatomegaly. |
| Radiodermatitis | |
| Flushing | |
| Chromosomal Instability | abnormalities of DNA metabolism, DNA repair, cell-cycle governance, or control of apoptosis that increase the probability that whole chromosomes or pieces of chromosomes are gained or lost during cell division, resulting in an imbalance in the number of chromosomes per cell (aneuploidy) and an enhanced rate of loss of heterozygosity |
| Fibrosis | |
| Lithiasis | |
| Siderosis | |
| Adolescent Psychology | |
| Arteriovenous Fistula | |
| Steatorrhea | |
| Sarcoma, Endometrial Stromal | |
| Melanosis | |
| Eye Infections, Viral | |
| Pulmonary Heart Disease | A congestive heart failure that involves a failure of the right side of the heart and is characterized by an enlargement of the right ventricle of the heart as a response to increased resistance or high blood pressure in the lungs. |
| Leukemia, Lymphocytic, Chronic | |
| Tonsillitis | An upper respiratory tract disease which involves inflammation of the tonsils resulting from bacterial (Group A streptococcus) and viral (Epstein-Barr virus, adenovirus) infections. Symptoms include a severe sore throat (which may be experienced as referred pain to the ears), painful/difficult swallowing, coughing, headache, myalgia (muscle aches), fever and chills. Tonsillitis is characterized by signs of red, swollen tonsils which may have a purulent exudative coating of white patches (i.e. pus). Swelling of the cheeks and neck may occur. |
| Presbycusis | |
| Leukemia, Promyelocytic, Acute | |
| Mitral Valve Stenosis | A mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart. |
| Leukemia, Myeloid | |
| Irritable Bowel Syndrome | A disorder with chronic or recurrent colonic symptoms without a clearcut etiology. This condition is characterized by chronic or recurrent ABDOMINAL PAIN, bloating, MUCUS in FECES, and an erratic disturbance of DEFECATION.|A syndrome that is a functional bowel disorder characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause. |
| Sarcopenia | |
| Meningeal Neoplasms | |
| Micronuclei, Chromosome-Defective | |
| Neuronal Ceroid-Lipofuscinoses | |
| Panuveitis | |
| Pancreatitis | Inflammation of the pancreas.|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. |
| Orientation | |
| Critical Illness | |
| Adrenocortical Hyperfunction | |
| Scleroderma, Diffuse | |
| Drug-Induced Liver Injury, Chronic | |
| Neuroleptic Malignant Syndrome | |
| Pseudopseudohypoparathyroidism | OMIM mapping confirmed by DO. [SN]. |
| von Hippel-Lindau Disease | OMIM mapping confirmed by DO. [LS]. |
| Appetite | |
| Maduromycosis | A dermatomycosis that effects skin and subcutaneous tissue located_in foot, located_in trunk, located_in buttocks, located_in eyelids, located_in lacrimal glands, located_in paranasal sinuses, located_in mandible, located_in scalp, located_in neck, located_in perineum, or located_in testes and has_symptom sinus discharge and results_in_formation_of nodules. |
| Otorhinolaryngologic Neoplasms | |
| Accelerated Idioventricular Rhythm | |
| Dystonic Disorders | |
| Enterocolitis, Pseudomembranous | |
| Asthma, Exercise-Induced | |
| Blood Coagulation Disorders, Inherited | |
| Keratosis, Actinic | |
| Plaque, Amyloid | |
| Memory, Short-Term | Remembrance of information for a few seconds to hours. |
| Hamartoma | A disordered proliferation of mature tissues that is native to the site of origin - eg, exostoses, nevi and soft tissue hamartomas. Although most hamartomas are benign, some histologic subtypes - eg, neuromuscular hamartoma, may proliferate aggressively such as mesenchymal cystic hamartoma, Sclerosing epithelial hamartoma, Sclerosing metanephric hamartoma. |
| Glaucoma, Open-Angle | |
| Urinary Bladder Neoplasms | |
| Anemia, Refractory | |
| Taste Threshold | |
| Romano-Ward Syndrome | An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles). |
| Teratoma | A germ cell and embryonal cancer that is an encapsulated tumor with tissue or organ components resembling normal derivatives of all three germ layers. |
| Microphthalmos | |
| Hepatitis C, Chronic | |
| Lymphoma, Mantle-Cell | |
| Hereditary Central Nervous System Demyelinating Diseases | |
| Androgen-Insensitivity Syndrome | A testicular disease and hermaphroditism that is characterized by the partial or complete inability of the cell to respond to androgens in individuals with a karyotype of 46,XY resulting in female physical traits but male genetic makeup. |
| Gingival Neoplasms | |
| Respiratory Paralysis | Inability to move the muscles of respiration. |
| Anus Neoplasms | |
| Nevus | |
| Lymphoma, B-Cell, Marginal Zone | |
| Graft Occlusion, Vascular | |
| Berylliosis | A pneumoconiosis that involves allergic response located_in lungs caused by inhalation of beryllium compounds. |
| Azoospermia | A condition of suboptimal concentration of SPERMATOZOA in the ejaculated SEMEN to ensure successful FERTILIZATION of an OVUM. In humans, oligospermia is defined as a sperm count below 20 million per milliliter semen. |
| Arnold-Chiari Malformation | Arnold-Chiari malformation consists of a downward displacement of the cerebellar tonsils and the medulla through the foramen magnum, sometimes causing hydrocephalus as a result of obstruction of CSF outflow. |
| Heart Failure, Diastolic | |
| Discrimination Learning | |
| Lambert-Eaton Myasthenic Syndrome | A neuromuscular junction disease that results from an abnormality of acetylcholine (ACh) release at the neuromuscular junction. It results from an autoimmune attack against voltage-gated calcium channels (VGCC) on the presynaptic motor nerve terminal. |
| 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. |
| Hemophilia A | |
| Hemophilia B | An inherited blood coagulation disease that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. |
| Arsenic Poisoning | |
| Graft vs Host Disease | |
| Probability Learning | |
| Prediabetic State | |
| Phenylketonuria, Maternal | |
| 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. |
| Obstetric Labor Complications | |
| Epidermolysis Bullosa Dystrophica | |
| Stuttering | An articulation disorder characterized by involuntary sound repetition and disruption or blocking of speech. |
| Cystinuria | An amino acid metabolic disorder that involves the formation of cystine stones in the kidneys, ureter, and bladder. |
| Headache Disorders, Primary | |
| Nasal Polyps | Polypoidal masses arising mainly from the mucous membranes of the nose and paranasal sinuses. They are freely movable and nontender overgrowths of the mucosa that frequently accompany allergic rhinitis. |
| Vertebrobasilar Insufficiency | |
| 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 (MeSH).|An autosomal dominant inherited form of amyloidosis.|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) |
| Breast Cyst | |
| Epilepsy, Absence | |
| Purpura, Thrombotic Thrombocytopenic | |
| Mucopolysaccharidosis IV | A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzymes galactose 6-sulfate sulfatase (Type A) or beta-galactosidase (Type B) needed to break down the keratan sulfate sugar chain. |
| Vaccinia | A viral infectious disease that results_in infection, located_in skin, has_material_basis_in Vaccinia virus, which is used as a live vaccine against smallpox. The virus is transmitted_by contact with the vaccination site before it has healed, or transmitted_by fomites that have been contaminated with live virus from the vaccination site. The infection has_symptom rash, has_symptom fever, and has_symptom body aches. |
| Nephrosclerosis | |
| Meningococcal Infections | Infections with bacteria of the species NEISSERIA MENINGITIDIS. |
| Cicatrix, Hypertrophic | |
| Hypokalemic Periodic Paralysis | OMIM mapping confirmed by DO. [SN]. |
| Obesity, Abdominal | |
| Polyradiculoneuropathy | |
| 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. |
| Criminal Psychology | |
| Creativeness | |
| Cerebellar Neoplasms | |
| Mercury Poisoning | |
| Nevus, Spindle Cell | |
| Intelligence Tests | |
| Parapsoriasis | |
| Epidermal Necrolysis, Toxic | |
| Conjunctival Diseases | |
| Digestive System Neoplasms | |
| Cerebrovascular Disorders | |
| Automatism | |
| Sepsis | Systemic disease associated with the presence of pathogenic microorganisms or their toxins in the blood.|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.|The presence of pathogenic microorganisms in the blood stream causing a rapidly progressing systemic reaction that may lead to shock. Symptoms include fever, chills, tachycardia, and increased respiratory rate. It is a medical emergency that requires urgent medical attention.|Septicemia caused by pyogenic microorganisms (e.g., STAPHYLOCOCCUS; BACILLUS), resulting in the formation of secondary foci of SUPPURATION and multiple ABSCESSES.|A disease of infectious agent resulting from the presence of pathogenic microbial agents, including pathogenic viruses, pathogenic bacteria, fungi, protozoa, multicellular parasites, and aberrant proteins known as prions. These pathogens are able to cause disease in animals and/or plants. Infectious pathologies are usually qualified as contagious disease (also called communicable disease) due to their potentiality of transmission from one person or species to another.|Sepsis associated with organ dysfunction distant from the site of infection. |
| Goiter, Nodular | |
| Rheumatic Nodule | |
| Smith-Lemli-Opitz Syndrome | OMIM mapping confirmed by DO. [LS]. |
| Ophthalmoplegia, Chronic Progressive External | |
| Anaphylaxis | anomaly in a reaction manifested by localized or generalized reaction that occurs immediately (minutes) after exposure to an antigen to which the person/animal was previously sensitized; it is IgE-mediated, and mast cell activation and degranulation are hallmarks |
| Uniparental Disomy | abnormal assortment of chromosomes from parent to offspring whereby the chromosome number is correct, but both members of a chromosome pair or segments of a chromosome pair are inherited from the same parent |
| Sleep Disorders, Intrinsic | |
| Candidiasis, Cutaneous | |
| Gonadal Dysgenesis, 46,XY | |
| Amyloid Neuropathies, Familial | |
| Neoplasm Seeding | |
| Thinking | |
| Paranasal Sinus Diseases | |
| Cystocele | When the tough fibrous wall between a woman's bladder and her vagina (the pubocervical fascia) is torn, allowing the bladder to herniate into the vagina. |
| Fructose Intolerance | |
| Mental Recall | |
| 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. |
| Fractures, Stress | |
| Glaucoma, Angle-Closure | |
| Cerebrovascular Accident | An artery disease that is characterized by dysfunction of the blood vessels supplying the brain. |
| DNA Repair-Deficiency Disorders | |
| Rheumatic Fever | |
| Keratosis Follicularis | OMIM mapping confirmed by DO. [SN]. |
| Pelizaeus-Merzbacher Disease | OMIM mapping confirmed by DO. [SN]. |
| Placental Insufficiency | A placenta disease that is characterized by insufficient blood flow to the placenta during pregnancy. |
| Hemoglobinuria | |
| Ileitis | An inflammatory bowel disease characterized by inflammation located_in ileum, has_symptom diarrhea, has_symptom abdominal pain, often in the right lower quadrant, has_symptom weight loss. |
| Respiratory Distress Syndrome, Adult | |
| Heart Failure, Systolic | |
| Ileal Diseases | |
| Chronic Disease | |
| Catatonia | |
| Puberty, Delayed | |
| Esophageal Diseases | |
| Fetal Growth Retardation | slow or limited development during the fetal period (sensu Mus: from E14 through birth) |
| Emmetropia | |
| Endocrine System Diseases | |
| Liver Neoplasms | |
| Factor VII Deficiency | |
| Arrhythmia, Sinus | |
| Neuropsychological Tests | Tests designed to assess neurological function associated with certain behaviors. They are used in diagnosing brain dysfunction or damage and central nervous system disorders or injury. |
| Psychometrics | |
| Wounds, Nonpenetrating | |
| Picornaviridae Infections | |
| Pseudarthrosis | |
| Tinea Capitis | A dermatophytosis that results_in contagious fungal infection located_in scalp, located_in hair of head, located_in eyebrow or located_in eyelash, has_material_basis_in Ascomycota fungi that belong to a group called dermatophytes and has_symptom itching of the scalp, has_symptom pus filled lesions on the scalp, and has_symptom patches of hair loss, sometimes with a 'black dot' pattern. |
| Farmer's Lung | An extrinsic allergic alveolitis which is induced by the inhalation of spores (Aspergillus sp and thermophilic actinomycetes) in dust from moldy hay or straw. It is characterized by sudden onset, fever, cough, expectoration, and breathlessness. |
| Body Image | |
| Pterygium | A fleshy mass of thickened conjunctiva that grows over part of the cornea usually from the inner side of the eyeball and causes a disturbance of vision. |
| Uterine Cervical Dysplasia | |
| Neoplasms, Ductal, Lobular, and Medullary | |
| Virilism | |
| Bladder Exstrophy | Eversion of the posterior bladder wall through the congenitally absent lower anterior abdominal wall and anterior bladder wall |
| Cerebral Ventricle Neoplasms | |
| Anemia, Hemolytic, Autoimmune | |
| Histoplasmosis | A primary systemic mycosis that results_in systemic fungal infection, has_material_basis_in Histoplasma capsulatum var capsulatum or has_material_basis_in Histoplasma capsulatum var duboisii, transmitted_by airborne spores and has_symptom nonproductive cough, has_symptom headache, has_symptom loss of appetite and has_symptom muscle pains. |
| Sudden Infant Death | |
| Syphilis | A primary bacterial infectious disease that is a sexually transmitted systemic disease, has_material_basis_in Treponema pallidum subsp pallidum, which is transmitted_by sexual contact, transmitted_by blood product transfusion, transmitted_by congenital method from mother to fetus or transmitted_by contact with infectious lesions. If left untreated, produces chancres, rashes, and systemic lesions in a clinical course with three stages continued over many years. |
| Insomnia, Fatal Familial | |
| Seasonal Affective Disorder | A mental depression that involves presentation of depressive symptoms only during a specific season of the year. |
| Meniere Disease | A vestibular disease characterized by vertigo, low-pitched tinnitus and hearing loss. |
| Retinal Hemorrhage | Hemorrhage occurring within the retina. |
| Psychosexual Development | |
| Psychomotor Agitation | |
| Sandhoff Disease | OMIM mapping confirmed by DO. [SN]. |
| Leukemia | A cancer that affects the blood or bone marrow characterized by an abnormal proliferation of blood cells.|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)|A malignant (clonal) hematologic disorder, involving hematopoietic stem cells and characterized by the presence of primitive or atypical myeloid or lymphoid cells in the bone marrow and the blood. Leukemias are classified as acute or chronic based on the degree of cellular differentiation and the predominant cell type present. Leukemia is usually associated with anemia, fever, hemorrhagic episodes, and splenomegaly. Common leukemias include acute myeloid leukemia, chronic myelogenous leukemia, acute lymphoblastic or precursor lymphoblastic leukemia, and chronic lymphocytic leukemia. Treatment is vital to patient survival; untreated, the natural course of acute leukemias is normally measured in weeks or months, while that of chronic leukemias is more often measured in months or years. |
| Malaria, Falciparum | |
| Fibroma | |
| Common Cold | An upper respiratory tract disease which involves inflammation of the mucous membranes of the nose, throat, eyes, and eustachian tubes with watery then purulent discharge. This is an acute contagious disease caused by rhinoviruses, human parainfluenza viruses, human respiratory syncytial virus, influenza viruses, adenoviruses, enteroviruses, or metapneumovirus. |
| Essential Tremor | A movement disorder that causes involuntary tremors, especially in the hands. It occurs alone without other neurological signs and symptoms. |
| Adenomyoma | A carcinosarcoma that has_material_basis_in gland and muscle components. |
| Human Engineering | |
| Sleep Disorders | |
| Cerebral Hemorrhage | Hemorrhage into the parenchyma of the brain. |
| Dental Occlusion, Traumatic | |
| Persian Gulf Syndrome | A syndrome affecting returning military veterans and civilian workers of the Gulf War. |
| Hypobetalipoproteinemias | |
| Leukoencephalitis, Acute Hemorrhagic | |
| Korsakoff Syndrome | OMIM mapping confirmed by DO. [LS]. |
| Fractures, Compression | |
| Gastroschisis | OMIM mapping confirmed by DO. [SN]. |
| Panic Disorder | An anxiety disorder that is characterized by unexpected and repeated episodes of intense fear accompanied by physical symptoms that may include chest pain, heart palpitations, shortness of breath, dizziness, or abdominal distress. |
| Arrhythmogenic Right Ventricular Dysplasia | An intrinsic cardiomyopathy that is characterized by hypokinetic areas involving the free wall of the right ventricle, with fibrofatty replacement of the right ventricular myocardium, with associated arrhythmias originating in the right ventricle. |
| Torsion Abnormality | |
| Uveitis, Posterior | |
| Amblyopia | |
| Adrenal Gland Neoplasms | |
| Hyperostosis, Diffuse Idiopathic Skeletal | |
| Hyperlipidemias | |
| Carcinoma, Adenoid Cystic | |
| Epidermolysis Bullosa | |
| Polycythemia | Abnormally high mass or concentration of red blood cells in the blood, either due to an increase in erythropoiesis or a decrease in plasma volume. |
| Staphylococcal Infections | |
| Favism | A glucosephosphate dehydrogenase deficiency characterized by a hemolytic reaction to consumption of broad beans. |
| Ataxia | |
| Poliomyelitis | A viral infectious disease that results_in destruction located_in motor neurons, has_material_basis_in Human poliovirus 1, has_material_basis_in Human poliovirus 2, or has_material_basis_in Human poliovirus 3, which are transmitted_by ingestion of food or water contaminated with feces, or transmitted_by direct contact with the oral secretions. The infection has_symptom fever, has_symptom sore throat, has_symptom headache, has_symptom vomiting, has_symptom fatigue, has_symptom neck stiffness, has_symptom muscle spasms, and has_symptom acute flaccid paralysis. |
| Neoplasm Invasiveness | |
| Abnormalities, Drug-Induced | |
| Reperfusion Injury | |
| Trail Making Test | |
| Thrombotic Microangiopathies | |
| Liver Failure, Acute | |
| Neointima | A new or thickened layer of arterial intima formed especially on a prosthesis or in atherosclerosis by migration and proliferation of cells from the media. |
| Leukemia, Myeloid, Chronic-Phase | |
| Anus, Imperforate | |
| Hip Dislocation, Congenital | |
| Parkinsonian Disorders | |
| Wasting Syndrome | |
| Leukemia, Lymphocytic | |
| von Willebrand Disease, Type 1 | |
| Fever | Elevated body temperature due to failed thermoregulation. |
| Mental Status Schedule | |
| Brachial Plexus Neuropathies | |
| Tuberculosis, Pulmonary | |
| Corneal Dystrophies, Hereditary | |
| Cystadenoma, Mucinous | |
| Libido | |
| Respiratory Hypersensitivity | |
| Subdural Effusion | |
| Object Attachment | |
| Down Syndrome | A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability. |
| Splenic Neoplasms | |
| Adenovirus Infections, Human | |
| Prostatic Hyperplasia | |
| Arthritis, Psoriatic | |
| Thyroid Diseases | |
| Duodenal Ulcer | Adding UMLS CUI for Curling Ulcer C0013295. |
| Tennis Elbow | |
| Diabetes Insipidus | |
| Personality Inventory | |
| Facial Asymmetry | An abnormal difference between the left and right sides of the face. |
| Lupus Vasculitis, Central Nervous System | |
| Peptic Ulcer | An ulcer of the gastrointestinal tract. |
| Pseudolymphoma | |
| Genetic Diseases, X-Linked | |
| Eosinophilia-Myalgia Syndrome | |
| Gastritis, Hypertrophic | |
| Anastomotic Leak | |
| Bacterial Infections | |
| Herpes Zoster | A viral infectious disease that results_in infection located_in nerve fiber, has_material_basis_in Human herpesvirus 3, which reactivates after appearing as chickenpox in childhood. The virus is transmitted_by direct contact with the rash, which can develop into chickenpox in newly-infected individuals. The infection has_symptom rash which is followed by blisters, has_symptom headache, has_symptom fever, has_symptom malaise, has_symptom itching, has_symptom burning pain, and has_symptom paresthesia. |
| Asymptomatic Diseases | |
| Urinary Incontinence | Loss of the ability to control the urinary bladder leading to involuntary urination. |
| Lead Poisoning, Nervous System, Adult | |
| Gallbladder Neoplasms | |
| Functional Laterality | Behavioral manifestations of cerebral dominance in which there is preferential use and superior functioning of either the left or the right side, as in the preferred use of the right hand or right foot. |
| Stress Disorders, Traumatic | |
| Rubinstein-Taybi Syndrome | An autosomal dominant disease characterized by short stature, moderate to sever intellectual disability, distinctive facial features and broad thumbs and first toes; additionally it can include eye abnormalities, heart and kidney defects, dental problems and obesity. |
| Rickets | A bone remodeling disease that has_material_basis_in a vitamin D deficiency in children which results_in softening and deformity located_in bone. |
| Pregnancy in Diabetics | |
| Pattern Recognition, Visual | |
| Aortic Coarctation | Coarctation of the aorta is a narrowing or constriction of a segment of the aorta. |
| Diabetes Mellitus | A metabolic disorder characterized by abnormally high blood sugar levels due to diminished production of insulin or insulin resistance/desensitization.|A heterogeneous group of disorders characterized by HYPERGLYCEMIA and GLUCOSE INTOLERANCE. |
| Nephritis, Hereditary | |
| Oligohydramnios | A placenta disease that is characterized by a deficiency of amniotic fluid sometimes resulting in an embryonic defect through adherence between embryo and amnion. |
| Arthritis, Gouty | |
| Muscle Spasticity | A motor disorder characterized by a velocity-dependent increase in tonic stretch reflexes with increased muscle tone, exaggerated (hyperexcitable) tendon reflexes. |
| Pneumothorax | |
| Blepharophimosis | |
| Fetal Membranes, Premature Rupture | |
| Thrombocytopenia, Neonatal Alloimmune | |
| Overweight | |
| Intestinal Polyps | A discrete abnormal tissue mass that protrudes into the lumen of the intestine and is attached to the intestinal wall either by a stalk, pedunculus, or a broad base. |
| Burning Mouth Syndrome | |
| Cognitive Reserve | |
| Retroperitoneal Fibrosis | |
| Diabetes Insipidus, Neurogenic | |
| Temporal Arteritis | OMIM mapping confirmed by DO. [LS]. |
| Thrombasthenia | |
| Amnesia, Transient Global | |
| Meningitis, Meningococcal | |
| Monosomy | one chromosome missing from an otherwise diploid chromosome set |
| Adenoma, Acidophil | |
| Inhalant Abuse | |
| Tachycardia, Ectopic Junctional | |
| Crohn Disease | An intestinal disease that involves inflammation located_in intestine. |
| 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. |
| Smooth Muscle Tumor | |
| Embryo Loss | |
| Testicular Neoplasms | |
| Intellectual Disability | A specific developmental disorder that involves significant limitations both in mental functioning and in adaptive behavior such as communicating, taking care of him or herself, and social skills. |
| Skin Neoplasms | |
| Chlamydophila Infections | |
| Trisomy | presence of an extra chromosome in an otherwise diploid chromosome set |
| Intermittent Claudication | |
| Vision, Low | |
| Alcohol Withdrawal Delirium | |
| Myositis, Inclusion Body | |
| Leprosy, Tuberculoid | |
| Conversion Disorder | A somatoform disorder that involves numbness, blindness, paralysis or fits without a neurological cause. |
| Seizures | Seizures are an intermittent abnormality of the central nervous system due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements. The term epilepsy is used to describe chronic, recurrent seizures. |
| Psychoses, Alcoholic | |
| Meningioma | A central nervous system cancer that are manifested in the central nervous system and arise from the arachnoid cap cells of the arachnoid villi in the meninges. |
| Glomerulosclerosis, Focal Segmental | |
| Kidney Calculi | |
| Liver Diseases, Alcoholic | |
| Hepatolenticular Degeneration | OMIM mapping confirmed by DO. [SN]. |
| Nephrolithiasis | Formation of stones in the KIDNEY. |
| Macular Edema | |
| Noonan Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Myoclonic Cerebellar Dyssynergia | OMIM mapping confirmed by DO. [SN]. |
| Pancreatic Diseases | |
| Muscular Dystrophy, Duchenne | A muscular dystrophy that has_material_basis_in X-linked disease caused by mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. |
| Neuroblastoma | A neuroblastic tumor characterized by the presence of neuroblastic cells, the absence of ganglion cells, and the absence of a prominent Schwannian stroma formation.|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)|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 (MeSH). |
| Dermatomycoses | |
| Adenoma | A neoplasm arising from the epithelium. It may be encapsulated or non-encapsulated but non-invasive. The neoplastic epithelial cells may or may not display cellular atypia or dysplasia. In the gastrointestinal tract, when dysplasia becomes severe it is sometimes called carcinoma in situ. Representative examples are pituitary gland adenoma, follicular adenoma of the thyroid gland, and adenomas (or adenomatous polyps) of the gastrointestinal tract.|A neoplasm arising from the epithelium. It may be encapsulated or non-encapsulated but non-invasive. The neoplastic epithelial cells may or may not display cellular atypia or dysplasia. In the gastrointestinal tract, when dysplasia becomes severe it is sometimes called carcinoma in situ. Representative examples are pituitary gland adenoma, follicular adenoma of the thyroid gland, and adenomas (or adenomatous polyps) of the gastrointestinal tract. |
| Histiocytosis, Langerhans-Cell | |
| Heat Stress Disorders | |
| alpha-Thalassemia | Alpha thalassemia is a thalassemia involving the genes HBA1and HBA2 hemoglobin genes. |
| Facial Pain | |
| Oropharyngeal Neoplasms | |
| Leukopenia | decrease in no. of leukocytes |
| Inflammatory Bowel Diseases | |
| Gerstmann-Straussler-Scheinker Disease | A prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain. |
| Metabolic Diseases | |
| Hemiplegia | |
| Hydrocephalus | A cerebral degeneration characterized by an abnormal accumulation of cerebrospinal fluid in the ventricles of the brain, leading to progressive enlargement of the head. |
| Bone Conduction | |
| Disorders of Sex Development | |
| Musculoskeletal Diseases | |
| Carotid Artery, Internal, Dissection | |
| Fallopian Tube Diseases | |
| Personal Autonomy | |
| Hereditary Sensory and Autonomic Neuropathies | |
| Osteonecrosis | Death of a bone or part of a bone, either atraumatic or posttraumatic. |
| Retroviridae Infections | |
| Glucosephosphate Dehydrogenase Deficiency | A carbohydrate metabolic disorder that is characterised by abnormally low levels of glucose-6-phosphate dehydrogenase (abbreviated G6PD or G6PDH). |
| Takotsubo Cardiomyopathy | Transient left ventricular apical ballooning syndrome or takotsubo cardiomyopathy is characterized by transient regional systolic dysfunction involving the left ventricular apex and/or mid-ventricle in the absence of obstructive coronary disease on coronary angiography. Patients present with an abrupt onset of angina-like chest pain, and have diffuse T-wave inversion, sometimes preceded by ST-segment elevation, and mild cardiac enzyme elevation. |
| Chromosome Duplication | |
| Carcinoma, Acinar Cell | |
| Psychology | |
| Phlebitis | A vein disease that is characterized by inflammation of a vein. |
| Ear Diseases | |
| Genital Diseases, Female | |
| Fetal Nutrition Disorders | |
| Adenomatous Polyposis Coli | |
| Waldenstrom Macroglobulinemia | A malignant monoclonal gammopathy characterized by a high level of an IgM monoclonal protein. |
| Thyroid Crisis | |
| Osteitis | A bone disease that results_in inflammation of the located_in bone. |
| Laryngostenosis | |
| Boutonneuse Fever | A spotted fever that has_material_basis_in Rickettsia conorii subsp conorii, which is transmitted_by dog tick (Rhipicephalus sanguineus). The infection has_symptom fever, has_symptom eschar (usually single), has_symptom regional adenopathy, has_symptom maculopapular rash on extremities. |
| Inflammation | |
| Angelman Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Awareness | |
| Arteriovenous Malformations | |
| Dwarfism, Pituitary | |
| Anthracosis | |
| Periapical Periodontitis | |
| Carbohydrate Metabolism, Inborn Errors | |
| Schizophrenia, Childhood | |
| Nasopharyngeal Neoplasms | |
| Epispadias | Displacement of the urethral opening on the dorsal (superior) surface of the penis. |
| Macular Edema, Cystoid | |
| Acatalasia | |
| Retinopathy of Prematurity | |
| Polymyalgia Rheumatica | |
| Carcinoma, Ductal | |
| Cushing Syndrome | An adrenal gland hyperfunction that is caused by overactivity of the adrenal cortex caused by a tumor of the pituitary gland. |
| Hepatitis, Autoimmune | |
| Hepatitis | |
| Uveomeningoencephalitic Syndrome | A hypersensitivity reaction type II disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis. |
| Uveitis | |
| Reinforcement Schedule | |
| Whipple Disease | |
| Status Epilepticus | |
| Glycogen Storage Disease Type V | OMIM mapping confirmed by DO. [SN]. |
| Encephalopathy, Bovine Spongiform | |
| Psychoneuroimmunology | |
| Periodontal Pocket | |
| Hemoglobinopathies | |
| Ureteral Obstruction | |
| Ossification of Posterior Longitudinal Ligament | |
| Glycogen Storage Disease Type I | A glycogen storage disease that has_material_basis_in deficiency of the glucose-6-phosphatase enzyme which impairs the ability of the liver to produce free glucose from glycogen and from gluconeogenesis and is characterized by accumulation of glycogen and fat in the liver and kidneys, resulting in hepatomegaly and renomegaly. |
| Lymphangiectasis | |
| Calcium Metabolism Disorders | |
| Peri-Implantitis | |
| Executive Function | |
| Legg-Calve-Perthes Disease | An osteochondrosis that results_in death and fracture located_in hip joint. |
| Vertigo | An abnormal sensation of spinning while the body is actually stationary. |
| ACTH-Secreting Pituitary Adenoma | A functioning pituitary adenoma that characterized by excess cortisol a primary cause of Cushing's syndrome. |
| Tuberculosis, Spinal | |
| Ovarian Hyperstimulation Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Burkitt Lymphoma | A mature B-cell neoplasm of B-cells found in the germinal center. |
| Schistosomiasis mansoni | |
| Immune System Diseases | |
| Kallmann Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Alveolar Bone Loss | |
| Job Syndrome | OMIM mapping confirmed by DO. [SN]. |
| Diplopia | Diplopia is a condition in which a single object is perceived as two images, it is also known as double vision. |
| Akathisia, Drug-Induced | |
| Eye Infections, Bacterial | |
| Psychopharmacology | |
| Cumulative Trauma Disorders | |
| Hidradenitis Suppurativa | OMIM mapping confirmed by DO. [SN]. |
| Tics | |
| Q Fever | A primary bacterial infectious disease that is a zoonotic infectious disease affecting multiple organs, has_material_basis_in Coxiella burnetii, which is transmitted_by inhalation of air contaminated by barnyard dust containing dried placental material, birth fluids, or excreta of infected herd animals, transmitted_by ingestion of contaminated milk, transmitted_by tick bites and transmitted_by contact with infected person. The infection has_symptom fever, has_symptom headache, has_symptom cough, has_symptom pleuritic chest pain, has_symptom myalgia and has_symptom arthralgia. |
| Alphavirus Infections | |
| Status Asthmaticus | An asthma that is a life threatening condition with progressive respiratory failure, which does not respond to standard treatment. |
| Spinocerebellar Degenerations | |
| Insulin Resistance | diminished effectiveness of insulin in lowering plasma glucose levels |
| Fatigue | A subjective feeling of tiredness characterized by a lack of energy and motivation. |
| Prurigo | |
| Lipodystrophy | |
| Leishmaniasis, Visceral | |
| Parapsychology | |
| Diabetes Mellitus, Type 1 | |
| Sick Sinus Syndrome | Xref MGI. |
| Diabetes Mellitus, Type 2 | |
| Infertility | Inability to reproduce after a specified period of unprotected intercourse. Reproductive sterility is permanent infertility. |
| Bundle-Branch Block | Block of conduction of electrical impulses along the Bundle of His or along one of its bundle branches. |
| Neural Tube Defects | any structural anomaly of or development of the hollow epithelial tube found on the dorsal side of the vertebrate embryo that develops into the central nervous system (i.e. brain and spinal cord) |
| Knowledge of Results | |
| Drug Toxicity | |
| Blood Group Incompatibility | |
| Blepharospasm | A focal dystonia that is characterized by the involuntary, forcible contraction of the muscles controlling eye blinks. |
| Pars Planitis | OMIM mapping confirmed by DO. [SN]. |
| Retinoschisis | |
| Immunologic Deficiency Syndromes | |
| Osteoporotic Fractures | |
| Sleep | Any process in which an organism enters and maintains a periodic, readily reversible state of reduced awareness and metabolic activity. Usually accompanied by physical relaxation, the onset of sleep in humans and other mammals is marked by a change in the electrical activity of the brain. |
| Extraversion | A state in which attention is largely directed outward from the self. |
| Byssinosis | |
| Lymphedema | |
| Heart Arrest | |
| Heart Diseases |
