MeSH Browser

MeSH Supplementary: Melanoma, Cutaneous Malignant
Unique ID: C562393
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562393
Entry Term(s): Dysplastic Nevus Syndrome, Hereditary; Familial Atypical Mole-Malignant Melanoma Syndrome; Famm; Melanoma, Familial
Registry Number: 0
Heading Mapped to: *Melanoma; *Skin Neoplasms
Frequency: 2899
Note: A primary melanoma that originates from atypical skin MELANOCYTES, especially from acquired and congenital MELANOCYTIC NEVI, and DYSPLASTIC NEVI. Different histologic types include superficial spreading melanoma, acral lentiginous melanoma, nodular melanoma, and lentigo maligna melanoma. Germline mutations in CDKN2A, CDK4, MC1R, and XRCC3 genes, and somatic mutations in BRAF, BAP1, GRIN2A, STK11, and PTEN genes have been identified. OMIM: 155600
Date of Entry: 2012/11/05
Revision Date: 2019/05/01

Concept UI: M0562693
Registry Number: 0
Terms: Melanoma, Cutaneous Malignant Preferred Term
Term UI T800608
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Famm
Term UI T000956568
Date05/01/2019
LexicalTag NON
ThesaurusID NLM (2019); Melanoma, Familial
Term UI T800613
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Dysplastic Nevus Syndrome, Hereditary
Term UI T800610
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Familial Atypical Mole-Malignant Melanoma Syndrome
Term UI T800612
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

Melanoma, Cutaneous Malignant MeSH Supplementary Concept Data 2023