amyloidosis
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 ]
Term info
- MESH:D000686 (Orphanet:69/e)
- MedDRA:10002022 (Orphanet:69/e)
- Orphanet:69 (MONDO:equivalentTo)
- SCTID:17602002 (MONDO:equivalentTo)
- UMLS:C0002726 (Orphanet:69/e)
- DOID:9120 (MONDO:equivalentTo)
- ICD9:277.3 (MONDO:i2s)
- HP:0011034 (MONDO:otherHierarchy)
- EFO:1001875 (MONDO:equivalentTo)
- ONCOTREE:MIDDA (MONDO:equivalentTo)
- ICD9:277.30 (MONDO:i2s)
- NCIT:C2868 (MONDO:equivalentTo)
disease_grouping, ordo_group_of_disorders
amyloidosis (disease)
http://identifiers.org/meddra/10002022
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.
http://purl.obolibrary.org/obo/DOID_9120, 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://purl.obolibrary.org/obo/Orphanet_69
amyloidosis (disease), amyloidosis, amyloid, amyloidoses, amyloid disease
MONDO:0019065