All terms in EFO
| Label | Id | Description |
|---|---|---|
| delivery method | EFO_0000395 | [A description of the method used to deliver e.g. a compound or solution for treatment.] |
| calcium channel blocker | CHEBI_38215 | [One of a class of drugs that acts by selective inhibition of calcium influx through cell membranes or on the release and binding of calcium in intracellular pools.] |
| dermal neurofibroma | EFO_0000397 | [A dermal neurofibroma is a neurofibroma that occurs in situ of the skin.] |
| dermatomyositis | EFO_0000398 | [Dermatomyositis (DM) is a type of idiopathic inflammatory myopathy characterized by evocative skin lesions and symmetrical proximal muscle weakness., 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)] |
| polymyositis | EFO_0003063 | [Polymyositis (PM) is a rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes., Polymyositis (PM)("inflammation of many muscles") is a type of chronic inflammation of the muscles (inflammatory myopathy) related to dermatomyositis and inclusion body myositis.] |
| obsolete_gnathodiaphyseal dysplasia | Orphanet_53697 | |
| obsolete_hyaline body myopathy | Orphanet_53698 | |
| Lethal arthrogryposis - anterior horn cell disease | Orphanet_53696 | |
| obsolete_GRACILE syndrome | Orphanet_53693 | [GRACILE syndrome is an inherited lethal mitochondrial disorder characterized by fetal growth restriction (GR), aminoaciduria (A), cholestasis (C), iron overload (I), lactacidosis (L), and early death (E).] |
| obsolete_congenital cornea plana | Orphanet_53691 | |
| dexamethasone | CHEBI_41879 | [A fluorinated steroid that has formula C22H29FO5.] |
| obsolete_congenital lactase deficiency | Orphanet_53690 | |
| 17q21.31 microdeletion syndrome | Orphanet_363958 | |
| sphinganine-1-phosphate | CHEBI_16893 | [A sphingoid 1-phosphate that is the monophosphorylated derivative of sphinganine.] |
| obsolete_corpus cardiacum | EFO_0000380 | [A pair of neurohemal organs located on the walls of the aorta just behind the brain. The corpora cardiaca release their store of PTTH only after they receive a signal from neurosecretory cells in the brain.] |
| obsolete_corpus striatum | EFO_0000381 | [Either of a pair of masses of nervous tissue within the brain that contain two large nuclei of gray matter separated by sheets of white matter., Striped gray and white matter consisting of the neostriatum and paleostriatum (globus pallidus). It is located in front of and lateral to the thalamus in each cerebral hemisphere. The gray substance is made up of the caudate nucleus and the lentiform nucleus. The white matter is the internal capsule. (MeSH)] |
| obsolete_corpus uteri | EFO_0000382 | |
| obsolete_cortex | EFO_0000383 | [The surface layer of gray matter of the cerebrum that functions chiefly in coordination of sensory and motor information.] |
| Crohn's disease | EFO_0000384 | [A gastrointestinal disorder characterized by chronic inflammation involving all layers of the intestinal wall, noncaseating granulomas affecting the intestinal wall and regional lymph nodes, and transmural fibrosis. Crohn disease most commonly involves the terminal ileum; the colon is the second most common site of involvement., A chronic transmural inflammation that may involve any part of the DIGESTIVE TRACT from MOUTH to ANUS, mostly found in the ILEUM, the CECUM, and the COLON. In Crohn disease, the inflammation, extending through the intestinal wall from the MUCOSA to the serosa, is characteristically asymmetric and segmental. Epithelioid GRANULOMAS may be seen in some patients.] |
| gingivitis | MONDO_0002508 | [A disorder involving inflammation of the gums; may affect surrounding and supporting structures of the teeth.] |