WNT10A

3 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 3 panels
Green WNT10A in Ectodermal dysplasia Version 3.29 Latest signed off version: v3.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Phenotypes Schopf-Schulz-Passarge syndrome, OMIM:224750 Odontoonychodermal dysplasia, OMIM:257980
Green WNT10A in Ectodermal dysplasia without a known gene mutation Level 3: Ectodermal dysplasias Level 2: Dermatological disorders Version 1.28	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Radboud University Medical Center, Nijmegen Illumina TruGenome Clinical Sequencing Services UKGTN Eligibility statement prior genetic testing Phenotypes Odontoonychodermal dysplasia, OMIM:257980 Schopf-Schulz-Passarge syndrome, OMIM:224750
Green WNT10A in Severe Paediatric Disorders Version 1.184	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Next Generation Children Project Expert Review Green Expert list Phenotypes Tooth agenesis, selective, 4, 150400 Schopf-Schulz-Passarge syndrome, 224750 Odontoonychodermal dysplasia, 257980