RAC3

Rac family small GTPase 3
OMIM: 602050
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies, 618577, Abnormality of brain morphology, Abnormal muscle tone, Neurodevelopmental delay, Intellectual disability, Abnormality of brain morphology, Abnormal muscle tone, Neurodevelopmental delay, Intellectual disability