WDFY3:Ensemblv115

WD repeat and FYVE domain containing 3
OMIM: 617485, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green WDFY3 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Victorian Clinical Genetics Services
  • Genetic Health Queensland
  • Expert Review Green
Phenotypes
  • Microcephaly 18, primary, autosomal dominant, MIM#617520

Green WDFY3 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • Microcephaly 18, primary, autosomal dominant, MIM#617520