Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
Merkel cell	CL_0000242
keratinocyte	CL_0000312
obsolete maternal pyrexia in labor	DOID_12284
stratified epithelial cell	CL_0000079
femoral vein thrombophlebitis	DOID_12282
buccal mucosa	UBERON_0006956
semi-lunar valve	UBERON_0005623
mesenteric artery	UBERON_0005616
intrahepatic gall duct cancer	DOID_12298
Vogt-Koyanagi-Harada disease	DOID_12297	[An autoimmune hypersensitivity 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.]
atypical depressive disorder	DOID_12294	[A mood disorder that is characterized by mood reactivity and positivity, significant weight gain or increased appetite, excessive sleep or somnolence, a sensation of heaviness in limbs known as leaden paralysis, and significant social impairment as a consequence of hypersensitivity to perceived interpersonal rejection.]
obsolete recurrent malignant endocervical neoplasm	DOID_12292
semisynthetic derivative	CHEBI_72588	[Any organic molecular entity derived from a natural product by partial chemical synthesis.]
mesonephric tubule	UBERON_0000083
distal hereditary motor neuronopathy type 2D	DOID_0111210	[A distal hereditary motor neuropathy type 2 that has_material_basis_in heterozygous mutation in FBXO38 on 5q32.]
distal hereditary motor neuronopathy type 2	DOID_0111206	[An autosomal dominant distal hereditary motor neuronopathy characterized by adult onset of slowly progressive distal atrophy and weakness.]
autosomal dominant centronuclear myopathy	DOID_0111217	[A centronuclear myopathy that has_material_basis_in autosomal dominant inheritance.]
Friedreich ataxia 1	DOID_0111218	[A Friedreich ataxia that has_material_basis_in homozygous or compound heterozygous mutation in FXN on 9q21.1.]
distal hereditary motor neuronopathy type 8	DOID_0111215	[A autosomal dominant distal hereditary motor neuronopathy characterized by congenital, non-progressive, predominantly distal, lower limb muscle weakness and atrophy with variable serverity that has_material_basis_in heterozygous mutation in TRPV4 on 12q24.11.]
autosomal recessive centronuclear myopathy	DOID_0111216	[A centronuclear myopathy that has_material_basis_in autosomal recessive inheritance.]