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Congenital hypogonadotropic hypogonadism

ORPHA:174590

Classification level: Group of disorders
  • Synonym(s): -
  • Prevalence: -
  • Inheritance: Autosomal dominant or Autosomal recessive or X-linked recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: -
  • OMIM: -
  • UMLS: C3899503
  • MeSH: -
  • GARD: -
  • MedDRA: 10083932

Summary

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Detailed information

Guidelines

Disease review articles

Genetic Testing

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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