Mitochondrial oxoglutarate/malate carrier deficiency

Synonym(s)
- Hereditary paraganglioma syndrome type 6
Type

Disease
External link(s)
- IEMbase
Gene
- SLC25A11 / Solute Carrier Family 25 Member 11
  17p13.2
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial carrier protein
Disease group(s)
- 11.1 Disorders of mitochondrial shuttles and carriers