WDFY3

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

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green WDFY3 in Autism Level 2: Neurology and neurodevelopmental disorders Version 0.205	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Microcephaly 18, primary, autosomal dominant, MIM#617520
Amber WDFY3 in Macrocephaly_Megalencephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 0.149	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Neurodevelopmental disorder with macrocephaly
Green WDFY3 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Microcephaly 18, primary, autosomal dominant, MIM#617520 Neurodevelopmental disorder with macrocephaly
Green WDFY3 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.295	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert list Phenotypes Microcephaly 18, primary, autosomal dominant, MIM#617520
Red WDFY3 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.108 Component of the following Super Panels: Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Literature Phenotypes Microcephaly 18, primary, autosomal dominant MIM#617520
Green WDFY3 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Victorian Clinical Genetics Services Phenotypes Microcephaly 18, primary, autosomal dominant, MIM#617520