Terminology Service < Semantic Lookup Platform

Label	Id	Description
GM04596 cell	CLO_0018886	[ CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED; CMTX1 GAP JUNCTION PROTEIN, BETA-1, 32-KD; GJB1]
ND02398 cell	CLO_0016223	[ ASYMPTOMATIC AND GENETICALLY RELATED TO AN AFFECTED INDIVIDUAL]
GM02135 cell	CLO_0031842	[ PORPHYRIA, ACUTE INTERMITTENT]
GM02137 cell	CLO_0031841	[ INVERTED CHROMOSOME]
GM04595 cell	CLO_0018887	[ GAP JUNCTION PROTEIN, BETA-1, 32-KD; GJB1 CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED; CMTX1]
ND02399 cell	CLO_0016222	[ POPULATION/CONVENIENCE CONTROL]
GM02138 cell	CLO_0031840	[ BASAL CELL NEVUS SYNDROME; BCNS]
GM04079 cell	CLO_0016225	[ FRIEDREICH ATAXIA 1; FRDA FRDA GENE; FRDA]
GM04587 cell	CLO_0018884	[ NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3 INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE-COMPLEX ASSOCIATED PROTEIN; IKBKAP]
GM04586 cell	CLO_0018885	[ NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE III; HSAN3 INHIBITOR OF KAPPA LIGHT POLYPEPTIDE GENE ENHANCER IN B CELLS, KINASE-COMPLEX ASSOCIATED PROTEIN; IKBKAP]
GM04081 cell	CLO_0016224	[ CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP]
carnitine uptake defect	DOID_1668
HQ00783 cell	CLO_0031835	[ HUNTINGTON DISEASE; HD]
Hs 908.Sk cell	CLO_0004216
IMG-807 cell	CLO_0006879
HQ00782 cell	CLO_0031834	[ HUNTINGTON DISEASE; HD]
IMG-797 cell	CLO_0006878
Hs 910.Sk cell	CLO_0004217
HQ00781 cell	CLO_0031833	[ HUNTINGTON DISEASE; HD]
IMG-796 cell	CLO_0006877