Genomics England
GMS Panels
Panels
Genes and Entities

NFASC

neurofascin
OMIM: 609145
PanelMode of inheritanceDetails
3 panels
Green
in Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with central and peripheral motor dysfunction, OMIM:618356, neurodevelopmental disorder with central and peripheral motor dysfunction, MONDO:0032698
Green
in Hereditary neuropathy or pain disorder
R-numbers: R78
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with central and peripheral motor dysfunction, OMIM:618356
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 9.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neurodevelopmental disorder with central and peripheral motor dysfunction, OMIM:618356, neurodevelopmental disorder with central and peripheral motor dysfunction, MONDO:003269