Menaquinone-4 synthetase deficiency

Synonym(s)
- Schnyder corneal dystrophy
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- UBIAD1 / UBIAD1
  1p36.22
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- UbiA prenyltransferase domain containing 1
Disease group(s)
- 21.11 Other disorders of vitamin metabolism