ZNF462

zinc finger protein 462
OMIM: 617371
PanelMode of inheritanceDetails
2 panels
R-numbers: R100
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Weiss-Kruszka syndrome, OMIM:618619, weiss-kruszka syndrome, MONDO:0032836
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Prominent metopic ridge, Ptosis, Ptosis, Prominent metopic ridge, Craniosynostosis, Global developmental delay, Intellectual disability, Autistic behavior, Intellectual disability, Global developmental delay, Craniosynostosis, Autistic behavior