WNT3

Wnt family member 3
OMIM: 165330, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red WNT3 in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE
  • TETAMS