All terms in NCIT
| Label | Id | Description |
|---|---|---|
| Apovincamine | NCIT_C74413 | |
| CDK11B wt Allele | NCIT_C49447 | [Human CDK11B wild-type allele is located in the vicinity of 3p21 and is approximately 31 kb in length. This allele, which encodes cyclin-dependent kinase 11B protein, plays a role in proliferation regulation, apoptosis and is essential for eukaryotic cell cycle control. The allele is deleted or altered frequently in neuroblastoma with amplified MYCN genes.] |
| CDK11B Gene | NCIT_C24280 | [This gene is involved in cell cycle control.] |
| Aminoethyl Nitrate | NCIT_C74414 | |
| PPP2R5E wt Allele | NCIT_C49448 | [Human PPP2R5E wild-type allele is located in the vicinity of 14q23.1 and is approximately 169 kb in length. This allele, which encodes serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform protein, plays a role in modulating both the substrate selectivity and catalytic activity of the core protein phosphatase 2A heterodimer.] |
| PPP2R5E Gene | NCIT_C20406 | [This gene plays a role in the negative control of cell growth and division.] |
| Manozodil | NCIT_C74415 | |
| PPP2R5A wt Allele | NCIT_C49441 | [Human PPP2R5A wild-type allele is located within 1q32.2-q32.3 and is approximately 76 kb in length. This allele, which encodes serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform protein, plays a role in modulating both the substrate selectivity and catalytic activity of the protein phosphatase 2A heterodimer.] |
| PPP2R5A Gene | NCIT_C20402 | [This gene plays a role in the negative control of cell growth and division.] |
| GAIA Maternal Immunization Level of Diagnostic Certainty | NCIT_C126867 | [A classification of maternal and fetal outcomes relating to maternal immunization, developed by the Global Alignment of Immunization safety Assessment in pregnancy, based on the extent to which the diagnosis has been confirmed.] |
| GAIA Neonatal Case Definitions | NCIT_C126830 | [A set of terms and defintions created by the Global Alignment of Immunization safety Assessment in pregnancy that are related to the neonatal effects of immunizations.] |
| BUB1 wt Allele | NCIT_C49442 | [Human BUB1 wild-type allele is located in the vicinity of 2q14 and is approximately 40 kb in length. This allele, which encodes mitotic checkpoint serine/threonine-protein kinase BUB1 protein, is involved in the regulation of spindle checkpoints and mitotic integrity. Mutations in this gene, which generate allelic variants have been associated with aneuploidy and several forms of cancer.] |
| BUB1 Gene | NCIT_C21494 | [This gene is a modulator of the mitotic spindle cell cycle checkpoint.] |
| Congenital Disorder of Glycosylation Type Ia | NCIT_C126868 | [A congenital disorder of glycosylation sub-type caused by mutation(s) in the PMM2 gene, encoding phosphomannomutase 2.] |
| PPP2R5B wt Allele | NCIT_C49443 | [Human PPP2R5B wild-type allele is located within 11q12-q13 and is approximately 10 kb in length. This allele, which encodes serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit beta isoform protein, is involved in modulating both the substrate selectivity and catalytic activity of the core protein phosphatase 2A heterodimer.] |
| PPP2R5B Gene | NCIT_C20403 | [This gene plays a role in the negative control of cell growth and division.] |
| Quincarbate | NCIT_C74410 | [A dioxinoquinolone-based diuretic and chemically distinct from the thiazide diuretics. Quincarbate was never marketed.] |
| Diuretic | NCIT_C448 | [A class of agents that increases the production of urine by the kidney. Via various mechanism of actions, diuretics retain water in urine, thus provides a means of forced diuresis.] |
| Congenital Disorder of Glycosylation Type Ic | NCIT_C126869 | [A congenital disorder of glycosylation sub-type caused by mutation(s) in the ALG6 gene, encoding dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase.] |
| PPP2R5C wt Allele | NCIT_C49444 | [Human PPP2R5C wild-type allele is located within 14q32 and is approximately 118 kb in length. This allele, which encodes serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform protein, plays a role in modulating both the substrate selectivity and catalytic activity of the core protein phosphatase 2A heterodimer.] |