WNT10A

Wnt family member 10A
OMIM: 606268, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green WNT10A in Desmosomal disorders Level 2: Dermatological disorders Version 0.33	review	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green WNT10A in Mendeliome Version 1.1891	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Odontoonychodermal dysplasia Schopf-Schulz-Passarge syndrome Tooth agenesis, selective, 4
Green WNT10A in Oligodontia Level 2: Dysmorphic and congenital abnormality syndromes Version 0.29	review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services 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 0.86	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Odontoonychodermal dysplasia, Tooth agenesis, selective, Schopf-Schulz-Passarge syndrome
Green WNT10A in Hair disorders Level 2: Dermatological disorders Version 0.71	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Odontoonychodermal dysplasia
Red WNT10A in Prepair 1000+ Level 2: Screening Version 1.9	review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Odontoonychodermal dysplasia 257980 AR Schopf-Schulz-Passarge syndrome 224750 AR Tooth agenesis, selective, 4 150400 AR, AD