DisGeNET - a database of gene-disease associations

Gene: WNT10A ×

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:	80326
Gene Symbol:	WNT10A

WNT10A

CUI:	C1857069
Disease:	SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)

SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)

0.770

GermlineCausalMutation

ORPHANET

WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

2009