WNT10A:Ensemblv115

Wnt family member 10A
OMIM: 606268, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green WNT10A in Desmosomal disorders Level 2: Dermatological disorders Version 1.0	1 review	Unknown	Sources Expert Review Green Victorian Clinical Genetics Services
Green WNT10A in Oligodontia Level 2: Dysmorphic and congenital abnormality syndromes Version 1.0	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert Review Green Phenotypes Odontoonychodermal dysplasia 257980 AR Schopf-Schulz-Passarge syndrome 224750 AR Tooth agenesis, selective, 4 150400 AR, AD
Green WNT10A in Ectodermal Dysplasia Level 2: Dermatological disorders Version 1.0	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Royal Melbourne Hospital Expert Review Green Phenotypes Odontoonychodermal dysplasia, Tooth agenesis, selective, Schopf-Schulz-Passarge syndrome
Green WNT10A in Hair disorders Level 2: Dermatological disorders Version 1.0	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Literature Expert Review Green Phenotypes Odontoonychodermal dysplasia
Red WNT10A in Prepair 1000+ Level 2: Screening Version 3.0	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Literature Expert Review Red Phenotypes Odontoonychodermal dysplasia 257980 AR Schopf-Schulz-Passarge syndrome 224750 AR Tooth agenesis, selective, 4 150400 AR, AD