corticosterone methyloxidase type 1 deficiency (Q55781638)

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human disease
  • Aldosterone deficiency 1
  • 18 alpha hydroxylase deficiency
  • Hyperreninemic Hypoaldosteronism, Familial, 1
  • CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY
  • CMO 1 deficiency
  • Corticosterone methyloxidase type 1 deficiency
  • 18-Hydroxylase Deficiency
  • Aldosterone Deficiency Due to Defect 1N Steroid 18-Hydroxylase
  • Aldosterone deficiency due to defect in 18 hydroxylase
  • 18 Hydroxylase deficiency
  • Steroid 18-Hydroxylase Deficiency
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Language Label Description Also known as
English
corticosterone methyloxidase type 1 deficiency
human disease
  • Aldosterone deficiency 1
  • 18 alpha hydroxylase deficiency
  • Hyperreninemic Hypoaldosteronism, Familial, 1
  • CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY
  • CMO 1 deficiency
  • Corticosterone methyloxidase type 1 deficiency
  • 18-Hydroxylase Deficiency
  • Aldosterone Deficiency Due to Defect 1N Steroid 18-Hydroxylase
  • Aldosterone deficiency due to defect in 18 hydroxylase
  • 18 Hydroxylase deficiency
  • Steroid 18-Hydroxylase Deficiency

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