WNT2B

Wnt family member 2B
OMIM: 601968, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green WNT2B in Intestinal failure or congenital diarrhoea


Version 2.2
Latest signed off version: v2.1 (23 Jun 2022)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Diarrhoea 9, OMIM:618168

Red WNT2B in Disorders of sex development

Level 3: Gonadal and sex development disorders
Level 2: Endocrine disorders
Version 3.2
Latest signed off version: v3.1 (23 Jun 2022)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Diarrhoea 9, OMIM:618168
  • 46,XX testicular disorder of sex development, MONDO:0100249

Amber WNT2B in Structural eye disease


Version 2.2
Latest signed off version: v2.1 (23 Jun 2022)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Diarrhoea 9, OMIM:618168
  • microcornea
  • coloboma, MONDO:0001476
Tags
  • watchlist