WNT10A, Wnt family member 10A, 80326

N. diseases: 136; N. variants: 41
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1857069
Disease: SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)
SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) 		0.770 Biomarker disease GENOMICS_ENGLAND
CUI: C1857069
Disease: SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)
SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) 		0.770 Biomarker disease CTD_human
CUI: C1857069
Disease: SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)
SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) 		0.770 GeneticVariation disease CLINVAR
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		0.730 Biomarker disease CTD_human
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		0.730 Biomarker disease GENOMICS_ENGLAND
CUI: C1835492
Disease: TOOTH AGENESIS, SELECTIVE, 4 (disorder)
TOOTH AGENESIS, SELECTIVE, 4 (disorder) 		0.610 Biomarker disease CTD_human
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.500 CausalMutation disease CLINVAR
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.500 GermlineCausalMutation disease ORPHANET
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.500 Biomarker disease HPO
CUI: C4082304
Disease: Oligodontia
Oligodontia 		0.500 GermlineCausalMutation disease ORPHANET
CUI: C4082304
Disease: Oligodontia
Oligodontia 		0.500 Biomarker disease HPO
CUI: C0406702
Disease: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 		0.300 GermlineCausalMutation disease ORPHANET
CUI: C1835493
Disease: Succedaneous Teeth, Agenesis Of
Succedaneous Teeth, Agenesis Of 		0.300 Biomarker disease CTD_human
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		0.200 Biomarker disease HPO
CUI: C1706004
Disease: Anhydrotic Ectodermal Dysplasias
Anhydrotic Ectodermal Dysplasias 		0.120 CausalMutation disease CLINVAR
CUI: C0040427
Disease: Tooth Abnormalities
Tooth Abnormalities 		0.110 Biomarker group HPO
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder) 		0.110 Biomarker disease HPO
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.110 Biomarker disease HPO
CUI: C1274743
Disease: Hyperhidrosis Palmaris Et Plantaris
Hyperhidrosis Palmaris Et Plantaris 		0.110 Biomarker disease HPO
CUI: C1290511
Disease: Anodontia of Permanent Dentition
Anodontia of Permanent Dentition 		0.110 Biomarker disease HPO
CUI: C0002170
Disease: Alopecia
Alopecia 		0.100 Biomarker disease HPO
CUI: C0002170
Disease: Alopecia
Alopecia 		0.100 CausalMutation disease CLINVAR
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.100 Biomarker disease HPO
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis 		0.100 Biomarker disease HPO
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis 		0.100 Biomarker disease HPO