WNT10A

Wnt family member 10A
OMIM: 606268, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green WNT10A in Ectodermal dysplasia


Version 1.26
Latest signed off version: v1.10 (15 Oct 2020)

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 1.22

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 1.84

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