Familial atypical multiple mole melanoma syndrome
ORPHA:404560· ICD-10 C43.9
Definition
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 and other malignancies.
- Prevalence
- Unknown
- Inheritance
- Autosomal dominant
- Age of onset
- All ages