WDR4

WD repeat domain 4
OMIM: 605924, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green WDR4 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Galloway-Mowat syndrome 6, OMIM #618347
  • Microcephaly, growth deficiency, seizures, and brain malformations, OMIM #618346

Green WDR4 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Galloway-Mowat syndrome 6 MIM#618347

Green WDR4 in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 0.522

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green WDR4 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Galloway-Mowat syndrome 6, OMIM #618347
  • Microcephaly, growth deficiency, seizures, and brain malformations, OMIM #618346

Green WDR4 in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Microcephaly, growth deficiency, seizures, and brain malformations, OMIM # 618346