amyloidosis
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. [ ]
Term info
amyloidosis
- amyloid
- amyloid disease
- amyloidoses
- amyloidosis
- amyloidosis (disease)
- systemic amyloidosis
disease_grouping, ordo_group_of_disorders
amyloidosis (disease)
https://icd.codes/icd10cm/E85.0, https://icd.codes/icd10cm/E85.1, https://icd.codes/icd10cm/E85.2, https://icd.codes/icd10cm/E85.3, https://icd.codes/icd10cm/E85.8, https://icd.codes/icd10cm/E85.9, https://icd.codes/icd10cm/E85.4
http://identifiers.org/meddra/10002022
http://purl.obolibrary.org/obo/DOID_9120, http://identifiers.org/mesh/D000686, http://purl.obolibrary.org/obo/NCIT_C2868, http://identifiers.org/snomedct/17602002, http://linkedlifedata.com/resource/umls/id/C0002726, http://purl.obolibrary.org/obo/Orphanet_69
EFO:1001875
Gautier Koscielny