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Late-onset familial hypoaldosteronism

Disease definition

A rare form of familial hypoaldosteronism characterized by adult onset of subnormal plasma aldosterone with elevated plasma renin activity, hyperkalemia, metabolic acidosis, and hypotension. Signs and symptoms are typically mild, and affected individuals may be clinically asymptomatic and diagnosed only after biochemical screening.

ORPHA:556037

Classification level: Subtype of disorder
  • Synonym(s):
    • Late-onset familial hyperreninemic hypoaldosteronism
    • Mild aldosterone synthase deficiency
  • Prevalence: Unknown
  • Inheritance: -
  • Age of onset: Adult, Elderly
  • ICD-10: E27.4
  • ICD-11: 5A73
  • OMIM: -
  • UMLS: C5680172
  • MeSH: -
  • GARD: -
  • MedDRA: -

  A summary on this disease is available in Español (2021) Français (2021) Nederlands (2021)

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The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.