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Microcephalic primordial dwarfism-insulin resistance syndrome

ORPHA:436182

Classification level: Disorder
  • Synonym(s): -
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Neonatal, Infancy, Childhood
  • ICD-10: Q87.1
  • OMIM: 616541  617253
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -
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