All terms in NCIT
| Label | Id | Description |
|---|---|---|
| Cutaneous Melanoma cN3 TNM Finding v7 | NCIT_C88404 | [Cutaneous melanoma with 1 or more metastatic nodes with in transit met(s)/satellite(s). (from AJCC 7th Ed.)] |
| Growth Hormone Deficiency | NCIT_C112835 | [Insufficient production of growth hormone.] |
| Cutaneous Melanoma Clinical Distant Metastasis TNM Finding v7 | NCIT_C88405 | [A clinical finding about one or more characteristics of cutaneous melanoma, following the rules of the TNM AJCC v7 classification system as they pertain to distant metastases. The clinical distant metastasis TNM findings for cutaneous melanoma include M0, M1a, M1b, and M1c. (from AJCC 7th Ed.)] |
| Thyroid Storm | NCIT_C112836 | [Acute onset of severe, life-threatening hyperthyroidism caused by a sudden release of excessive thyroid hormone.] |
| Cutaneous Melanoma cM0 TNM Finding v7 | NCIT_C88406 | [Cutaneous melanoma with no detectable evidence of distant metastases. (from AJCC 7th Ed.)] |
| QPRT Gene | NCIT_C112837 | [This gene is involved in cofactor nucleotide metabolism.] |
| Nucleotide Biosynthesis Process | NCIT_C41545 | [Nucleotide Biosynthesis consists of activities of biologic molecules or complexes involved in the enzymatic formation of nucleoside phosphates, the monomeric building blocks from which DNA or RNA polymers are constructed.] |
| Cutaneous Melanoma cM1 TNM Finding v7 | NCIT_C88407 | [Cutaneous melanoma with detectable evidence of distant metastases. (from AJCC 7th Ed.)] |
| QPRT wt Allele | NCIT_C112838 | [Human QPRT wild-type allele is located in the vicinity of 16p11.2 and is approximately 20 kb in length. This allele, which encodes nicotinate-nucleotide pyrophosphorylase [carboxylating] protein, plays a role in NAD biosynthesis.] |
| Nicotinate and Nicotinamide Metabolism Pathway | NCIT_C38838 | |
| Cutaneous Melanoma cNX TNM Finding v7 | NCIT_C88400 | [Cutaneous melanoma in which the regional lymph nodes cannot be assessed (e.g., previously removed for another reason). (from AJCC 7th Ed.)] |
| Ichthyosis Acquisita | NCIT_C112831 | [A non-hereditary form of ichthyosis characterized by plate-like scales on the legs, arms and occasionally the torso.] |
| Ichthyosis | NCIT_C84776 | [A group of inherited or acquired skin disorders characterized by a dry, thickened, and scaly skin. The skin changes range from mild to severe.] |
| Cutaneous Melanoma cN0 TNM Finding v7 | NCIT_C88401 | [Cutaneous melanoma in which no regional metastases are detected. (from AJCC 7th Ed.)] |
| Copine-1 | NCIT_C112832 | [Copine-1 (537 aa, ~59 kDa) is encoded by the human CPNE1 gene. This protein plays a role in both calcium binding and vesicle trafficking.] |
| Cutaneous Melanoma cN1 TNM Finding v7 | NCIT_C88402 | [Cutaneous melanoma with macrometastasis in one regional lymph node. Macrometastases are defined as clinically detectable nodal metastases confirmed by therapeutic lymphadenectomy or when nodal metastasis exhibits gross extracapsular extension. (from AJCC 7th Ed.)] |
| Tinea Versicolor | NCIT_C112833 | [A skin condition characterized by hypopigmented, pink or tan, confetti-like, discrete and confluent scaly macules distributed on the chest, shoulders and upper back.] |
| Cutaneous Melanoma cN2c TNM Finding v7 | NCIT_C88403 | [Cutaneous melanoma with intralymphatic metastases (in transit or satellite metastases) without metastatic nodes. (from AJCC 7th Ed.)] |
| Growth Hormone Excess | NCIT_C112834 | [Overproduction of growth hormone, a protein-based peptide that stimulates growth, cell reproduction, and cell regeneration.] |
| TSC1 Gene Inactivation | NCIT_C40462 | [A mutation in the TSC1 gene that either inhibits the expression of or results in the translation of an inactive hamartin protein.] |