ABHD16A deficiency

Synonym(s)
- Autosomal recessive spastic paraplegia type 86
Type

Disease
External link(s)
- Orphanet
Gene
- ABHD16A / abhydrolase domain containing 16A
  6p21.33
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Abhydrolase domain-containing protein 16A
Disease group(s)
- 14.5.1 Disorders of phosphatidylcholine, phosphatidylserine and phosphatidylethanolamine metabolism