SNX14 deficiency

Synonym(s)
- Autosomal recessive spinocerebellar ataxia type 2
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SNX14 / Sorting Nexin 14
  6q14.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Sorting nexin-14
Disease group(s)
- 20.5 Disorders of autophagy