A classification for rare disorders of diverse organ systems (endocrine, neuromuscular, gastrointestinal, renal, dermatologic, rheumatologic, hematologic) that are affected by substances secreted by a distant neoplasm but not by the action of the neoplasm itself metastasizing to that organ or tissue. Less than 1 % of neoplasms are associated with these syndromes. An immune-mediated response to neoplasm-elaborated proteins may be the cause of these syndromes. Additionally, their manifestation may signal the presence of an occult neoplasm, potentially at an earlier stage of disease thereby leading to a better clinical outcome. Constitutional signs may include fever, night sweats, anorexia and cachexia. Clinical course is usually progressive. Prognosis is variable depending on the effective treatment of the underlying neoplasm. [ NCIT:C3311 ]

Synonyms: paraneoplastic syndrome

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Term information

database cross reference
  • MEDGEN:45320 (MONDO:equivalentTo)
  • NCIT:C3311 (MONDO:equivalentTo)
  • SCTID:49783001 (MONDO:equivalentTo)
  • UMLS:C0030472 (MONDO:equivalentTo)
  • MESH:D010257 (MONDO:equivalentTo)
exactMatch

http://purl.obolibrary.org/obo/NCIT_C3311

http://identifiers.org/mesh/D010257

http://linkedlifedata.com/resource/umls/id/C0030472

http://identifiers.org/snomedct/49783001

http://identifiers.org/medgen/45320

id

MONDO:0021073

Term relations