Mitochondrial 10-formyltetrahydrofolate dehydrogenase deficiency

Type

Disease
External link(s)
- IEMbase
Gene
- ALDH1L2 / Aldehyde Dehydrogenase 1 Family Member L2
  12q23.3
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Aldehyde dehydrogenase 1 family member L2
Disease group(s)
- 21.8 Disorders of folate metabolism