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Non-acquired isolated growth hormone deficiency

ORPHA:631

  • Synonym(s):
    • Congenital IGHD
    • Congenital isolated GH deficiency
    • Congenital isolated growth hormone deficiency
  • Prevalence: 1-5 / 10 000
  • Inheritance: Autosomal dominant or Autosomal recessive or X-linked recessive 
  • Age of onset: Neonatal
  • ICD-10: E23.0
  • OMIM: 173100  262400  262650  300123  307200  612781
  • UMLS: C0013338  C0271561
  • MeSH: -
  • GARD: 12556
  • MedDRA: 10035083

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