Melanoma, cutaneous malignant, susceptibility to, 9

Preferred Label : Melanoma, cutaneous malignant, susceptibility to, 9;

Symbol : CMM9;

CISMeF acronym : CMM9;

Type : Phenotype, molecular basis known;

Description : Malignant melanoma is a neoplasm of pigment-producing cells called melanocytes that occurs most often in the skin, but may also occur in the eyes, ears, gastrointestinal tract, leptomeninges, and oral and genital mucous membranes (summary by Habif, 2010). For a discussion of genetic heterogeneity of malignant melanoma, see 155600.;

Prefixed ID : #615134;

Détails

Origin ID

615134;

UMLS CUI

C3554574;

Automatic exact mappings (from CISMeF team)
- TERT wt Allele [NCIt concept]
Genes related to phenotype
- Telomerase reverse transcriptase [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Melanoma [HPO term]
ORDO concept(s)
- Familial melanoma [ORDO Disease]
Semantic type(s)
- Finding [UMLS semantic type]

Position du mot-clé dans l'(les) arborescence(s) :

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