Hydroxysteroid sulfotransferase deficiency

Synonym(s)
- Autosomal recessive congenital ichthyosis type 14
Type

Disease
External link(s)
- IEMbase
Gene
- SULT2B1 / sulfotransferase family 2B member 1
  19q13.33
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Sulfotransferase 2B1
Disease group(s)
- 24.2 Disorders of steroid metabolism