SCAF4

SR-related CTD associated factor 4
OMIM: 616023
PanelMode of inheritanceDetails
2 panels
R-numbers: R59
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
SCAF4-related Neurodevelopmental Disorder, Intellectual disability, Seizures, Behavioural abnormalities
Component of the following Super Panels:
  • - White matter disorders - childhood onset
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
SCAF4-related Neurodevelopmental Disorder, Intellectual disability, Seizures, Behavioural abnormalities