Mitochondrial pyrimidine nucleotide carrier deficiency

Synonym(s)
- Familial hyperinsulinemic hypoglycemia type 8
Type

Disease
Gene
- SLC25A36 / Solute Carrier Family 25 Member 36
  3q23
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial carrier protein SLC25A36
Disease group(s)
- 11.1 Disorders of mitochondrial shuttles and carriers