WDR5

WD repeat domain 5
OMIM: 609012, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber WDR5 in Speech apraxia


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review
  • Expert Review Amber
Phenotypes
  • Neurodevelopmental disorder (MONDO:0700092), WDR5-related