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amyloidosis

Go to external page http://purl.obolibrary.org/obo/MONDO_0019065

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. [ NCIT:C2868 ]

Synonyms: amyloidosis (disease) amyloidosis amyloid amyloidoses amyloid disease

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:277.30 (MONDO:i2s)
  • SCTID:17602002 (MONDO:equivalentTo)
  • HP:0011034 (MONDO:otherHierarchy)
  • MEDGEN:272 (MONDO:equivalentTo)
  • MedDRA:10002022 (Orphanet:69/e)
  • ICD9:277.3 (MONDO:i2s)
  • Orphanet:69 (MONDO:equivalentTo)
  • MESH:D000686 (Orphanet:69/e)
  • ONCOTREE:MIDDA (MONDO:equivalentTo)
  • GARD:18676 (MONDO:GARD)
  • icd11.foundation:2078467774 (Orphanet:69)
  • EFO:1001875 (MONDO:equivalentTo)
  • NANDO:2200138 (https://orcid.org/0000-0003-0011-764X)
  • DOID:9120 (MONDO:equivalentTo)
  • NCIT:C2868 (MONDO:equivalentTo)
  • UMLS:C0002726 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders

OBO foundry unique label

amyloidosis (disease)

closeMatch

http://identifiers.org/meddra/10002022

exactMatch

http://purl.obolibrary.org/obo/DOID_9120

http://www.orpha.net/ORDO/Orphanet_69

http://purl.obolibrary.org/obo/NCIT_C2868

http://identifiers.org/mesh/D000686

http://identifiers.org/snomedct/17602002

http://linkedlifedata.com/resource/umls/id/C0002726

http://identifiers.org/medgen/272

id

MONDO:0019065

Term relations