WDR47:Ensemblv115

WD repeat domain 47
OMIM: 615734, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green WDR47 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Complex neurodevelopmental disorder MONDO:0100038, WDR47-related

Green WDR47 in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Complex neurodevelopmental disorder MONDO:0100038, WDR47-related