CYP4F22 omega hydroxylase deficiency

Synonym(s)
- Autosomal recessive congenital ichthyosis type 5
Type

Disease
External link(s)
- IEMbase
Gene
- CYP4F22 / Cytochrome P450 Family 4 Subfamily F Member 22
  19p13.12
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Cytochrome P450 4F22
Disease group(s)
- 14.6 Disorders of sphingolipid synthesis and recycling