Genomics England
GMS Panels
Panels
Genes and Entities

NEUROG1

neurogenin 1
OMIM: 601726
PanelMode of inheritanceDetails
1 panel
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Cranial dysinnervation disorder, congenital, with absent corneal reflex and developmental delay, OMIM:620469