Genomics England
GMS Panels
Panels
Genes and Entities

RFX3

regulatory factor X3
OMIM: 601337
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
RFX3-related neurodevelopmental disorder with autism and other behavioural abnormalities, complex neurodevelopmental disorder, MONDO:0100038
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 10.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Intellectual disability, MONDO:0001071, Autism spectrum disorder, MONDO:0005258, Attention deficit-hyperactivity disorder, MONDO:0007743