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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 19/12/06 |
| Symbol | FAMMMPC | |||||||||
| Location | 9p21.3 | |||||||||
| Name | familial atypical multiple mole melanoma-pancreatic carcinoma | |||||||||
| Other name(s) | melanoma - pancreatic cancer syndrome | |||||||||
| Corresponding gene | CDKN2A | |||||||||
Genetic determination
| Related entries
| MNST
| Function/system disorder
| dermatology |
| digestive tract/liver and annex |
| neoplasia | Type
| susceptibility factor
| |
| Remark(s) | CDKN2A-Leiden mutation 19 bp deletion in exon 2 of the p16 gene (p16-Leiden). |