amyloidosis https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/amyloidosis NCIT:C2868 amyloid NANDO:2200138 amyloidoses ICD10CM:E85 UMLS:C0002726 SCTID:17602002 amyloid disease DOID:9120 MESH:D000686 MONDO:0019065 Orphanet:69 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. ICD9:277.3 GARD:0018676 MEDGEN:272 amyloidosis (disease) ONCOTREE:MIDDA MedDRA:10002022 EFO:1001875 icd11.foundation:2078467774 amyloidosis (disease) amyloidosis ICD9:277.30 ICD10WHO:E85 HP:0011034 proteostasis deficiencies