ARHGEF9

Cdc42 guanine nucleotide exchange factor 9
OMIM: 300429
PanelMode of inheritanceDetails
2 panels
R-numbers: R59
Signed-off version 2.2
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes
Epileptic encephalopathy, early infantile, 8 300607
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 3.2
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Phenotypes
Epileptic encephalopathy, early infantile, 8, 300607, EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 8