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Amyloidosis

Disease ID: disease_node_1155

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DbxrefICD10CM:E85, ICD9CM:277.3, MESH:D000686, NCI:C2868, SNOMEDCT_US_2023_03_01:154769007, UMLS_CUI:C0002726
SubclassofDOID_0014667
Data SourceDOID, MESH
Synonymsamyloid disease
Mesh IdD000686
Mesh LabelAmyloidosis
Mesh SubclassofD057165
Doid Labelamyloidosis
Doid DescriptionA disease of metabolism that is characterized by extracellular tissue deposition of mis-folded amyloid fibrils built up by twisted protofilaments, deposited in the spaces between the cells of vital organs, causing disruption of organ tissue structure and function. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition. amyloidosis has both inherited and acquired subtypes [LS].
Disease Node Iddisease_node_1155
Doid IdDOID_9120
LabelAmyloidosis