Genomics England
GMS Panels
Panels
Genes and Entities
PDYN
prodynorphin
OMIM:
131340
See this entity in PanelApp
Panel
Mode of inheritance
Details
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Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
- Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 6.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Spinocerebellar ataxia 23