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Familial isolated hypoparathyroidism due to impaired PTH secretion

ORPHA:189466

Classification level: Subtype of disorder
  • Synonym(s): -
  • Prevalence: -
  • Inheritance: Autosomal dominant or Autosomal recessive 
  • Age of onset: -
  • ICD-10: E20.8
  • OMIM: 146200
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

This disease is described under Familial isolated hypoparathyroidism

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