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X-linked lymphoproliferative disease

^ http://www.orpha.net/ORDO/Orphanet_2442


X-linked lymphoproliferative disease is a hereditary immunodeficiency characterized, in the majority of cases, by an inadequate immune response to infection with the Epstein-Barr virus (EBV).

Synonyms: Duncan disease, XLP, Purtilo syndrome

Term info

database cross reference
  • MeSH:D008232 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:308240 (E (exact mapping (the terms and the concepts are equivalent)))
  • ICD-10:D82.3 (Specific code (The term has its own code in the ICD10))
  • MedDRA:10068348 (E (exact mapping (the terms and the concepts are equivalent)))
  • UMLS:C0549463 (E (exact mapping (the terms and the concepts are equivalent)))
  • OMIM:300635 (BTNT (broader term maps to a narrower term))
  • ICD-10:D82.3 (E (exact mapping (the terms and the concepts are equivalent)))
hasDbXref

MedDRA:10068348, UMLS:C0549463, ICD-10:D82.3, MeSH:D008232, OMIM:308240, OMIM:300635

notation

ORPHA:2442