Terminology Service < Semantic Lookup Platform

Label	Id	Description
supravalvular aortic stenosis	DOID_1929
DA05757 cell	CLO_0036307	[ DIABETES MELLITUS FAMILY SAMPLE]
GM17427 cell	CLO_0012336	[ COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4]
osteogenesis imperfecta type I	DOID_14708
ND10161 cell	CLO_0036302	[ ALS PANEL CAUCASIAN FROM THE US AMYOTROPHIC LATERAL SCLEROSIS]
GM17426 cell	CLO_0012335	[ COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4]
immortal human arm-derived fibroblast cell line cell	CLO_0000395
GM02664 cell	CLO_0014990	[ GILLES DE LA TOURETTE SYNDROME; GTS]
Gilles de la Tourette syndrome	DOID_11119
ND10160 cell	CLO_0036301	[ EPILEPSY]
GM17425 cell	CLO_0012334	[ COLLAGEN, TYPE I, ALPHA-2; COL1A2 OSTEOGENESIS IMPERFECTA, TYPE IV; OI4]
GM02665 cell	CLO_0014991	[ APPARENTLY HEALTHY NON-FETAL TISSUE]
ND10163 cell	CLO_0036304	[ AVM-RUPTURED]
Arteriovenous Malformations, Cerebral	DOID_12429
GM17424 cell	CLO_0012333	[ EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2; ERCC2 TRICHOTHIODYSTROPHY; TTD ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH RETARDATION, INCLUDED XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D; XPD]
IBIDS syndrome	DOID_2960
DA05552 cell	CLO_0014992	[ DIABETES MELLITUS FAMILY SAMPLE]
ND10162 cell	CLO_0036303	[ AVM-UNRUPTURED]
GM50194 cell	CLO_0014993	[ CHROMOSOME DELETION CRI-DU-CHAT SYNDROME]
ND09351 cell	CLO_0012332	[ SPOUSAL CONTROL DNA CONTROL PANEL FOR LATE ONSET PARKINSON'S; UNAFFECTED INDIVIDUALS]