Terminology Service < Semantic Lookup Platform

All terms in CLO

Label	Id	Description
ND06759 cell	CLO_0018857	[ TRANSIENT ISCHEMIC ATTACK]
ND06758 cell	CLO_0018858	[ POPULATION/CONVENIENCE CONTROL DNA CONTROL PANEL FOR LATE ONSET PARKINSON'S; UNAFFECTED INDIVIDUALS]
ND06760 cell	CLO_0018855	[ NDPT080 ISCHEMIC STROKE DNA PANEL ISCHEMIC STROKE]
GM16092 cell	CLO_0018856	[ XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC]
GM16089 cell	CLO_0018859	[ LIG4 SYNDROME]
DNA ligase IV deficiency	DOID_0060021	["A combined T cell and B cell immunodeficiency that is caused by a mutatino in the LIG4 gene, a DNA ligase, encoding a protein essential for V(D)J recombination and DNA double-strand break (DSB) repair through nonhomologous end joining (NHEJ). Patients present with immunodeficiency and developmental and growth delay." [url:http\://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606593, url\]:http\://www.ncbi.nlm.nih.gov/gene/3981?]]
GM04516 cell	CLO_0018850	[ SIDEROBLASTIC ANEMIA - 269950 OR 301300]
HQ00779 cell	CLO_0031831	[ HUNTINGTON DISEASE; HD]
GM16094 cell	CLO_0018853	[ COCKAYNE SYNDROME, TYPE I; CKN1]
GM02110 cell	CLO_0031830	[ HYPERCHOLESTEROLEMIA, FAMILIAL; FHC]
GM16093 cell	CLO_0018854	[ XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC]
GM04515 cell	CLO_0018851	[ SIDEROBLASTIC ANEMIA - 269950 OR 301300]
ND06761 cell	CLO_0018852	[ ISCHEMIC STROKE]
Hs 916 cell	CLO_0004227
GM02098 cell	CLO_0031824	[ BASAL CELL NEVUS SYNDROME; BCNS]
neural keel	UBERON_0007135
IMG-827 cell	CLO_0006889
Hs 917.T cell	CLO_0004228	[disease: benign sebaceous cyst]
immortal human parotid gland-derived cell line cell	CLO_0000872
GM02099 cell	CLO_0031823	[ BASAL CELL NEVUS SYNDROME; BCNS]