Sterol carrier protein 2 deficiency

Synonym(s)
- Leukoencephalopathy with dystonia and motor neuropathy
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SCP2 / SCP2 lipid transfer protein
  1p32.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Sterol carrier protein 2
Disease group(s)
- 14.2 Disorders of peroxisomal fatty acid oxidation