All terms in EFO
| Label | Id | Description |
|---|---|---|
| obsolete_tuberculosis | EFO_0000774 | [Any of the infectious diseases of man and other animals caused by species of MYCOBACTERIUM., A chronic, recurrent infection caused by the bacterium Mycobacterium tuberculosis. Tuberculosis (TB) may affect almost any tissue or organ of the body with the lungs being the most common site of infection. The clinical stages of TB are primary or initial infection, latent or dormant infection, and recrudescent or adult-type TB. Ninety to 95% of primary TB infections may go unrecognized. Histopathologically, tissue lesions consist of granulomas which usually undergo central caseation necrosis. Local symptoms of TB vary according to the part affected; acute symptoms include hectic fever, sweats, and emaciation; serious complications include granulomatous erosion of pulmonary bronchi associated with hemoptysis. If untreated, progressive TB may be associated with a high degree of mortality. This infection is frequently observed in immunocompromised individuals with AIDS or a history of illicit IV drug use. --2004] |
| magnetic affinity cell sorting | EFO_0009109 | [A method of cell sorting that uses paramagnetic beads that are coated with antibodies, antigens, receptors, receptor substrates, binding proteins, etc to separate target cells from solution.] |
| Whipple's disease | EFO_0000775 | [A chronic systemic infection by a gram-positive bacterium, Tropheryma whippelii, mainly affecting the SMALL INTESTINE but also the JOINTS; CARDIOVASCULAR SYSTEM; and the CENTRAL NERVOUS SYSTEM. The disease is characterized by fat deposits in the INTESTINAL MUCOSA and LYMPH NODES, malabsorption, DIARRHEA with fatty stools, MALNUTRITION, and ARTHRITIS., A systemic infection caused by the Gram-positive bacterium Tropheryma whipplei. It affects the small intestine resulting in malabsorption. Other sites or systems affected by the infection are the joints, central nervous system, and the cardiovascular system.] |
| Aeromonas hydrophila infection | EFO_0000776 | [Aeromonas hydrophila infection is a bacterial disease caused by infection from the Aeromonas hydrophila bacteria.] |
| human granulocytic anaplasmosis | EFO_0000777 | [An ehrlichiosis that results_in infection located_in granular leukocyte, has_material_basis_in Anaplasma phagocytophilum, which is transmitted_by lone start tick (Amblyomma americanum ). The infection has_symptom headache, has_symptom muscle aches, has_symptom fatigue, has_symptom fever and has_symptom rash, A tick-borne, infectious disease caused by Anaplasma phagocytophilum, an obligate intracellular bacterium that is typically transmitted to humans by ticks of the Ixodes ricinus species complex.] |
| anaplasmosis | MONDO_0025303 | [An disease or disorder caused by infection with Anaplasma.] |
| ehrlichiosis | MONDO_0016003 | [Human ehrlichiosis and anaplasmosis describe a group of acute febrile tick-borne diseases characterized by an overlapping clinical picture that includes fever, headache, myalgias, arthralgias, skin eruptions, gastrointestinal symptoms and neurological manifestations. Diseases in this group include human monocytotropic ehrlichiosis (HME), human granulocytotropic anaplasmosis (HGA), and human ehrlichiosis ewingii (HEE).] |
| Amblyomma americanum | NCBITaxon_6943 | |
| neutrophil | CL_0000775 | [Any of the immature or mature forms of a granular leukocyte that in its mature form has a nucleus with three to five lobes connected by slender threads of chromatin, and cytoplasm containing fine inconspicuous granules and stainable by neutral dyes.] |
| obsolete_muscular dystrophy | EFO_0000757 | [An atrophic muscular disease that causes progressive weakness and degeneration of skeletal muscles used during voluntary movement.] |
| obsolete_limb-girdle muscular dystrophy | EFO_0000758 | [A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).] |
| neuropeptide S | CHEBI_53461 | |
| lipoma | EFO_0000759 | [A benign, usually painless, well-circumscribed lipomatous tumor composed of adipose tissue.] |
| bulbospinal muscular atrophy of adulthood | MONDO_0016115 | [A bulbospinal muscular atrophy that occurs in an adult.] |
| intermediate Charcot-Marie-Tooth disease | MONDO_0018778 | |
| obsolete_periodic paralysis with transient compartment-like syndrome | Orphanet_397755 | |
| generalized bulbospinal muscular atrophy | MONDO_0016116 | |
| obsolete_retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies | Orphanet_397758 | |
| metabolic myopathy | MONDO_0020123 | [A group of rare inherited disorders characterized by a deficiency of enzymes that are involved in metabolic pathways that affect muscles. The disorders are characterized by muscle dysfunction.] |
| muscular glycogenosis | MONDO_0016118 |