| ISA | CONGENITAL-ANOMALY SKIN-DISEASE |
| ANCESTORS | ALL CHANGE-STATE CHANGE-STATE-ANIMAL CONGENITAL-ANOMALY DISEASE-EVENT EVENT LIVING-EVENT PHYSICAL-EVENT SKIN-DISEASE |
| FAMMM syndrome | term type: main entry term part of speech: noun number: singular reliability code: 9 definition: autosomal dominant disease characterized by the familial occurrence of malignant melanoma of the skin and multiple atypical precursor lesions. (en) |
| Familial atypical multiple mole melanoma syndrome | definition: see FAMMM. (en) term type: full form part of speech: noun number: singular reliability code: 9 |
| nevus atípico familiar | definition: enfermedad autosomal dominante caracterizada por la presencia de melanoma maligno de origen familiar y lesiones atípicas precursoras. (es) gender: masculine number: singular term type: main entry term part of speech: noun |