DisGeNET - a database of gene-disease associations

Source: ORPHANET

Disease: Familial Atypical Mole Melanoma Syndrome ×

Gene: CDKN2A ×

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	1029
Gene Symbol:	CDKN2A

CDKN2A

CUI:	C2314896
Disease:	Familial Atypical Mole Melanoma Syndrome

Familial Atypical Mole Melanoma Syndrome

0.400

SusceptibilityMutation

ORPHANET

Genetic risk factors for melanoma.

2009