NPTX1

neuronal pentraxin 1
OMIM: 602367
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 5.3
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Spinocerebellar ataxia 50, OMIM:620158