Mitochondrial ATP-Mg/phosphate transporter deficiency

Synonym(s)
- Gorlin-Chaudhry-Moss syndrome,
- Fontaine syndrome
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- SLC25A24 / solute carrier family 25 member 24
  1p13.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Mitochondrial carrier protein
Disease group(s)
- 11.1 Disorders of mitochondrial shuttles and carriers
Child entries
- Progeroid syndrome, Petty type