corticosterone methyloxidase type 1 deficiency

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Synonyms

  • 18 Hydroxylase deficiency
  • 18 alpha hydroxylase deficiency
  • 18-Hydroxylase deficiency
  • 18-hydroxycorticosterone dehydrogenase deficiency
  • 18-hydroxylase deficiency
  • CAH - 18-hydroxylase deficiency
  • CMO 1 deficiency
  • CMO I deficiency
  • CMO II deficiency
  • aldosterone deficiency 1
  • aldosterone deficiency due to 18-hydroxylase defect
  • aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency
  • aldosterone deficiency due to defect in 18 hydroxylase
  • aldosterone deficiency due to defect in steroid 18-Hydroxylase
  • corticosterone 18-monooxygenase deficiency
  • corticosterone methyl oxidase type I deficiency
  • corticosterone methyl oxidase type II deficiency
  • corticosterone methyloxidase type 1 deficiency
  • corticosterone methyloxidase type I deficiency
  • hyperreninemic hypoaldosteronism, familial, 1
  • hypoaldosteronism, congenital, due to cmo i deficiency
  • steroid 18-hydroxylase deficiency

GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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