MELANOMA MULTIPLE MOLE SYNDROME 1
GPTKB entity
Statements (20)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
genetic disorder
|
| gptkbp:alsoKnownAs |
FAMMM syndrome
Familial Atypical Multiple Mole Melanoma Syndrome |
| gptkbp:associatedWith |
increased risk of melanoma
multiple atypical moles |
| gptkbp:diagnosedBy |
genetic testing
clinical criteria |
| gptkbp:firstDescribed |
1978
|
| https://www.w3.org/2000/01/rdf-schema#label |
MELANOMA MULTIPLE MOLE SYNDROME 1
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:managedBy |
genetic counseling
mole removal if suspicious regular skin examinations |
| gptkbp:mutationAssociatedWith |
gptkb:CDKN2A_gene
|
| gptkbp:OMIM |
155601
|
| gptkbp:prevalence |
rare
|
| gptkbp:riskFactor |
pancreatic cancer
|
| gptkbp:symptom |
dysplastic nevi
|
| gptkbp:bfsParent |
gptkb:p16
|
| gptkbp:bfsLayer |
7
|