Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete Tympanosclerosis of tympanic membrane and ossicles	DOID_1213
meninx of spinal cord	UBERON_0003292
childhood central nervous system primitive neuroectodermal neoplasm	DOID_3870
obsolete medulloblastoma with leptomeningeal spread	DOID_3871
obsolete leptomeningeal metastases	DOID_3872
nodular medulloblastoma	DOID_3873
extratemporal epilepsy	DOID_2544	[An epilepsy syndrome that is located_in an area of the brain other than the temporal lobe.]
colonic pseudo-obstruction	DOID_3876
functional colonic disease	DOID_3877
obsolete congenital epilepsy	DOID_2545
dicrocoeliasis	DOID_1219	[A parasitic helminthiasis infectious disease that involves parasitic infection of the bile ducts of the liver by Dicrocoelium dendriticum. The symptoms include cholecystitis, liver abscesses and upper abdominal pain.]
obsolete atonic epilepsy	DOID_2546
echinostomiasis	DOID_1218	[A parasitic helminthiasis infectious disease that involves parasitic infection of the intestine by Echinostoma species. The symptoms include nausea, vomiting, diarrhea, fever and abdominal pain.]
fascioloidiasis	DOID_1217	[A parasitic helminthiasis infectious disease that involves parasitic infection of the liver of a variety of wild and domestic ruminants by Fascioloides magna.]
intestinal pseudo-obstruction	DOID_3878
obsolete intractable epilepsy	DOID_2547
diffuse alopecia areata	DOID_0060157	[An alopecia areata that involves diffuse loss of hair over the whole scalp.]
Joubert syndrome 17	DOID_0110986	[A Joubert syndrome characterized by episodic hyperpnea, abnormal eye movements, ataxia, and global psychomotor retardation that has_material_basis_in compound heterozygous mutation in the C5ORF42 gene on chromosome 5p13.]
Joubert syndrome 18	DOID_0110987	[A Joubert syndrome that has_material_basis_in homozygous mutation in the TCTN3 gene on chromosome 10q24.]
Joubert syndrome 15	DOID_0110984	[A Joubert syndrome characterized by ataxia, hypotonia, delayed psychomotor development, and variable mental retardation that has_material_basis_in homozygous mutation in the CEP41 gene on chromosome 7q32.]