Genomics England
GMS Panels
Panels
Genes and Entities

SP9

Sp9 transcription factor
PanelMode of inheritanceDetails
1 panel
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
complex neurodevelopmental disorder, MONDO:0100038, SP9-related neurodevelopmental disorder with or without epileptic encephalopathy