Terminology Service < Semantic Lookup Platform

All terms in NCIT

Label	Id	Description
TX Stage Finding	NCIT_C48737	[A primary tumor TNM finding indicating that the status of the primary tumor cannot be assessed.]
IPSS Risk Category Intermediate-2	NCIT_C139303	[An International Prognostic Scoring System for Myelodysplastic Syndrome risk category that predicts a high-interdemiate likelihood for progression.]
pM1 Stage Finding	NCIT_C48741
Pathologic Distant Metastasis TNM Finding	NCIT_C48886	[A pathologic finding about one or more characteristics of a specific cancer, following the rules of the TNM classification system as they pertain to staging of distant metastases.]
pM1a Stage Finding	NCIT_C48742
pM1b Stage Finding	NCIT_C48743
pM1c Stage Finding	NCIT_C48744
pM0 Stage Finding	NCIT_C48740	[No morphologic evidence of distant metastasis, in accordance with TNM classification system guidelines.]
Bathtub Seat Usually Used	NCIT_C130967	[A response indicating that an individual usually uses a bathtub seat.]
Bathtub Bar Usually Used	NCIT_C130968	[A response indicating that an individual usually uses a bathtub bar.]
Long-handled Appliances in Bathroom Usually Used	NCIT_C130969	[A response indicating that an individual usually uses a long-handled appliance in the bathroom.]
Embryonic	NCIT_C34100
Have Very Mild Bloating	NCIT_C130981	[A response indicating that when an individual has or had bloating, it was very mild.]
Allantois	NCIT_C34101	[An extraembryonic membrane in the form of a sac. It collects waste from the embryo.]
10p13-p14 Deletion Syndrome	NCIT_C130982	[A congenital condition caused by a deletion on the short arm of chromosome 10p13-p14. The NEBL gene, encoding nebulette, a heart-specific component of the sarcomere, may be responsible for the clinical findings. The condition is characterized by immunodeficiency, unusual facies, congenital heart anomalies (tetralogy of Fallot, pulmonary atresia with ventricular septal defect, truncus arteriosus, interrupted aortic arch, isolated anomalies of the aortic arch, and ventricular septal defect), hypoparathyroidism, and increased susceptibility to infections.]
Amniotic Cavity	NCIT_C34102	[The fluid-filled space within the amnion that contains the developing fetus.]
Amniotic Sac	NCIT_C34103	[The transparent extraembryonic sac that holds the developing fetus and surrounding amniotic fluid.]
Barakat Syndrome	NCIT_C130983	[A condition characterized by hypoparathyroidism, sensorineural deafness, and renal failure. It is related to autosomal dominant inactivating mutation(s) in GATA3, encoding a transcription factor important for the embryonic development of the parathyroid gland, the auditory stem, and the kidneys.]
GATA3 Gene	NCIT_C75492	[This gene plays a role in the modulation of transcription.]
Amnion	NCIT_C12365	[The innermost layer of membrane that surrounds an embryo and amniotic fluid in mammals, birds, and reptiles.]