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Hypochondrogenesis

ORPHA:93297

Classification level: Subtype of disorder
  • Synonym(s): -
  • Prevalence: Unknown
  • Inheritance: Autosomal dominant 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q77.0
  • ICD-11: LD24.51
  • OMIM: 200610
  • UMLS: C0542428
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

This disease is described under Achondrogenesis

Detailed information

Disease review articles

ERN : produced/endorsed by ERN(s)
FSMR : produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

Newborn screening

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