WDR4

WD repeat domain 4
OMIM: 605924
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Microcephaly, growth deficiency, seizures, and brain malformations, OMIM:618346
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Galloway-Mowat syndrome 6, OMIM:61834, Microcephaly, growth deficiency, seizures, and brain malformations, OMIM:618347
R-numbers: R88
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Galloway-Mowat syndrome 6, OMIM:61834, Microcephaly, growth deficiency, seizures, and brain malformations, OMIM:618347