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GTR Home > Conditions/Phenotypes > Familial atypical multiple mole melanoma syndrome


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. [from ORDO]

Available tests

2 tests are in the database for this condition.

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Genes See tests for all associated and related genes

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