17-alpha hydroxylase/17,20-lyase deficiency

Synonym(s)
- Congenital adrenal hyperplasia due to 17-alpha hydroxylase deficiency deficiency
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- CYP17A1 / Cytochrome P450 Family 17 Subfamily A Member 1
  10q24.32
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Cytochrome P450 17A1
Disease group(s)
- 24.2 Disorders of steroid metabolism
Child entries
- CYP17A1-related DSD