Familial atypical multiple mole melanoma syndrome

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Familial atypical multiple mole melanoma (FAMMM) syndrome is an inherited genodermatosis characterized by the presence of multiple melanocytic nevi (often >50) and a family history of melanoma as well as, in a subset of patients, an increased risk of developing pancreatic cancer (see this term) and other malignancies.

Synonyms: Familial atypical mole syndrome FAMMM syndrome Melanoma-pancreatic cancer syndrome FAMM-PC syndrome Familial atypical multiple mole melanoma-pancreatic carcinoma syndrome Familial dysplastic nevus syndrome B-K mole syndrome

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Term information

database cross reference
hasDbXref

UMLS:C0205747

ICD-10:C43.9

UMLS:C2314896

UMLS:C1838547

OMIM:606719

UMLS:C0013403

OMIM:155600

notation

ORPHA:404560