Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
WHODAS 2.0 36-item Version Self-administered - Making New Friends	NCIT_C130828	[World Health Organization Disability Assessment Schedule 2.0 36-item Version Self-administered (WHODAS 2.0 36-item Version Self-administered) In the past 30 days, how much difficulty did you have in: Making new friends?]
Choroid Disorder	NCIT_C34468	[A non-neoplastic or neoplastic disorder that affects the choroid. Representative examples include choroiditis, hemangioma, and melanoma.]
Choroid	NCIT_C12344	[A blood vessel-containing membrane of the eye that lies between the retina and the sclera.]
WHODAS 2.0 36-item Version Self-administered - Sexual Activities	NCIT_C130829	[World Health Organization Disability Assessment Schedule 2.0 36-item Version Self-administered (WHODAS 2.0 36-item Version Self-administered) In the past 30 days, how much difficulty did you have in: Sexual activities?]
Choroideremia	NCIT_C34469	[A rare, X-linked inherited disorder characterized by choroid atrophy and retinal degeneration. It leads to progressive loss of vision.]
5-Hydroxytryptamine Receptor 1A	NCIT_C105870	[5-hydroxytryptamine receptor 1A (422 aa, ~46 kDa) is encoded by the human HTR1A gene. This protein is involved in both serotonin binding and neurotransmitter-mediated signal transduction.]
Closed Dislocation of Hip	NCIT_C34485	[A closed dislocation of the hip.]
Hip Dislocation	NCIT_C34698	[A congenital or traumatic abnormality in which the femoral head slips out of the acetabulum.]
NEUROG1 wt Allele	NCIT_C105860	[Human NEUROG1 wild-type allele is located within 5q23-q31 and is approximately 2 kb in length. This allele, which encodes neurogenin-1 protein, is involved in both transcriptional regulation and neuronal differentiation.]
5q23-q31	NCIT_C13775	[A chromosome band present on 5q]
Closed Dislocation of Shoulder	NCIT_C34486	[A closed dislocation of the shoulder]
Neurogenin-1	NCIT_C105861	[Neurogenin-1 (237 aa, ~26 kDa) is encoded by the human NEUROG1 gene. This protein plays a role in both neuron differentiation and the regulation of gene expression.]
Closed Dislocation, Multiple and Ill-Defined Sites	NCIT_C34487	[Multiple bone displacements without clear distinction that are not associated with an external wound.]
UGT1A9 Gene	NCIT_C105862	[This gene is involved in phenol detoxification.]
WHODAS 2.0 36-item Version Self-administered - Problem Living with Dignity	NCIT_C130840	[World Health Organization Disability Assessment Schedule 2.0 36-item Version Self-administered (WHODAS 2.0 36-item Version Self-administered) In the past 30 days: How much of a problem did you have living with dignity because of the attitudes and actions of others?]
Closed Fracture of Carpal Bone	NCIT_C34488	[A traumatic break in one or more of the carpal bones that does not involve a break in the adjacent skin.]
UGT1A9 wt Allele	NCIT_C105863	[Human UGT1A9 wild-type allele is located in the vicinity of 2q37 and is approximately 101 kb in length. This allele, which encodes UDP-glucuronosyltransferase 1-9 protein, plays a role in the detoxification of phenolic compounds.]
WHODAS 2.0 36-item Version Self-administered - Time Spend on Your Health Condition	NCIT_C130841	[World Health Organization Disability Assessment Schedule 2.0 36-item Version Self-administered (WHODAS 2.0 36-item Version Self-administered) In the past 30 days: How much time did you spend on your health condition, or its consequences?]
Churg-Strauss Syndrome	NCIT_C34481	[An autoimmune necrotizing vasculitis with the formation of granulomas. It is a pulmonary and systemic vasculitis associated with eosinophilia.]
UDP-Glucuronosyltransferase 1-9	NCIT_C105864	[UDP-glucuronosyltransferase 1-9 (530 aa, ~60 kDa) is encoded by the human UGT1A9 gene. This protein is involved in the metabolism of phenolic compounds.]