RFX3

regulatory factor X3
OMIM: 601337
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Intellectual disability, MONDO:0001071, Autism spectrum disorder, MONDO:0005258, Attention deficit-hyperactivity disorder, MONDO:0007743