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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
Detailed information
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- Clinical practice guidelines
- Français (2017)
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