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Isolated growth hormone deficiency type III

ORPHA:231692

Classification level: Subtype of disorder
  • Synonym(s):
    • Congenital IGHD type III
    • Congenital isolated GH deficiency type III
    • Congenital isolated growth hormone deficiency type III
    • X-linked IGHD
    • X-linked isolated growth hormone deficiency
  • Prevalence: -
  • Inheritance: X-linked recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: E23.0
  • OMIM: 300123  307200
  • UMLS: -
  • MeSH: -
  • GARD: 3921
  • MedDRA: -

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.

Additional information

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