RALA

RAS like proto-oncogene A
OMIM: 179550
PanelMode of inheritanceDetails
2 panels
R-numbers: R59
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Global developmental delay, Intellectual disability, Seizures, Abnormality of nervous system morphology
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
Global developmental delay, Seizures, Abnormality of nervous system morphology, Global developmental delay, Intellectual disability, Seizures, Abnormality of nervous system morphology, Intellectual disability