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Isolated growth hormone deficiency type III

ORPHA:231692

  • 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: -

Additional information

Further information on this disease

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