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Turner syndrome due to structural X chromosome anomalies

ORPHA:99413

Classification level: Subtype of disorder
  • Synonym(s): -
  • Prevalence: -
  • Inheritance: -
  • Age of onset: Antenatal, Neonatal, Infancy, Childhood
  • ICD-10: Q96.1  Q96.2
  • ICD-11: LD50.01  LD50.02
  • OMIM: -
  • UMLS: C5681631
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

This disease is described under Turner syndrome

Detailed information

Guidelines

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

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.