OnlineIMD

CYP11B2-related disease

  • Type
    Disease
  • External link(s)
    • IEMbase
  • Gene
    • CYP11B2 / Cytochrome P450 Family 11 Subfamily B Member 2
      • 8q24.3
      • OMIM
      • GnomAD
      • Ensembl
      • HGNC
      • VMH
      • LOVD
  • Gene product
    • Aldosterone synthase
  • Disease group(s)
    • 24.2    Disorders of steroid metabolism
  • Child entries
    • Corticosterone methyloxidase deficiency
    • Corticosterone methyloxidase deficiency type 1
    • Corticosterone methyloxidase deficiency type 2
    • Familial hyperaldosteronism type 1