Genomics England
GMS Panels
Panels
Genes and Entities

PDYN

prodynorphin
OMIM: 131340
PanelMode of inheritanceDetails
1 panel
Green
in Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 4.40
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Spinocerebellar ataxia 23