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Isolated growth hormone deficiency type IB


Classification level: Subtype of disorder
  • Synonym(s):
    • Congenital IGHD type IB
    • Congenital isolated GH deficiency type IB
    • Congenital isolated growth hormone deficiency type IB
  • Prevalence: -
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: E23.0
  • OMIM: 612781  618157
  • UMLS: C2748571
  • MeSH: -
  • GARD: 3919
  • MedDRA: -
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