Source: ORPHANET

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. 19559398

2009
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		0.730 GermlineCausalMutation ORPHANET Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations. 24458874

2014
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		0.730 GermlineCausalMutation ORPHANET Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. 17847007

2007
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.500 GermlineCausalMutation ORPHANET

Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A
CUI: C4082304
Disease: Oligodontia
Oligodontia 		0.500 GermlineCausalMutation ORPHANET

Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A
CUI: C1275074
Disease: Odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia 		0.370 GermlineCausalMutation ORPHANET Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations. 24458874

2014
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A
CUI: C1275074
Disease: Odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia 		0.370 GermlineCausalMutation ORPHANET Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia. 17847007

2007
Entrez Id: 80326
Gene Symbol: WNT10A
WNT10A
CUI: C0406702
Disease: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 		0.300 GermlineCausalMutation ORPHANET