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De Sanctis-Cacchione syndrome

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ORPHA:1569

Classification level: Disorder

Synonym(s):
  • Xeroderma pigmentosum with neurologic manifestation

Prevalence: -

Inheritance: -

Age of onset:

OMIM: 278800

UMLS: C0265201

MeSH: C535992

GARD: 8276

Summary

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Xeroderma pigmentosum

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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