VPS13C deficiency

Synonym(s)
- Autosomal recessive Parkinson disease type 23
Type

Disease
External link(s)
- IEMbase
Gene
- VPS13C / VPS13C
  15q22.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Vacuolar protein sorting 13C
Disease group(s)
- 19.5 Disorders of organelle interplay