About: Amyloidosis     Goto   Sponge   Distinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Amyloidosis
equivalentClass
Concept_In_Subset
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Amyloidosis
UMLS_CUI
  • C0002726
Contributing_Source
  • CDISC
  • CTEP
ALT_DEFINITION
  • A group of diseases in which protein builds up in certain organs (localized amyloidosis) or throughout the body (systemic amyloidosis). Amyloidosis may be either primary (with no known cause), secondary (caused by another disease, including some types of cancer, such as multiple myeloma), or hereditary (passed down from parents to children). Many organs are affected by amyloidosis. The organs affected may depend on whether the amyloidosis is the primary, secondary, or hereditary form.NCI-GLOSS
  • A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands.CDISC
Legacy_Concept_Name
  • Amyloidosis
FULL_SYN
  • AmyloidosisPTNCI
  • amyloidosisPTNCI-GLOSSCDR0000045507
  • AmyloidosisPTCDISC
  • AmyloidosisPTCTEP10002024
DEFINITION
  • A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands.NCI
code
  • C2868
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