WDR18

WD repeat domain 18
ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red WDR18 in Mendeliome


Version 1.3795

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Cornelia de Lange syndrome (MONDO:0016033)

Red WDR18 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.497

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Cornelia de Lange syndrome - MONDO:0016033