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| Term | amyloidosis | ID (Ontology) | DOID:9120 (Human Disease) |
| Definition | A 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. | ||
| Also Known As | "amyloid disease" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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disease |__disease of metabolism |__amyloidosis 61 rec. |__apolipoprotein A-IV associated amyloidosis |__cerebral amyloid angiopathy 11 rec. | |__APP-related cerebral amyloid angiopathy 2 rec. | |__CST3-related cerebral amyloid angiopathy 3 rec. | |__ITM2B-related cerebral amyloid angiopathy 1 3 rec. | |__ITM2B-related cerebral amyloid angiopathy 2 3 rec. |__dialysis-related amyloidosis |__familial visceral amyloidosis 4 rec. |__immunoglobulin heavy chain amyloidosis |__immunoglobulin heavy-and-light chain |__immunoglobulin light chain amyloidosis |__primary cutaneous amyloidosis 2 rec. | |__Finnish type amyloidosis 2 rec. | |__primary localized cutaneous amyloidosis 1 | |__primary localized cutaneous amyloidosis 2 | |__primary localized cutaneous amyloidosis 3 |__serum amyloid A amyloidosis |__transthyretin amyloidosis 24 rec. |__variant ABeta2M amyloidosis |__wild-type amyloidosis |
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| Is a | disease of metabolism | ||
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ICD10CM:E85 ICD9CM:277.3 MESH:D000686 NCI:C2868 SNOMEDCT_US_2023_03_01:154769007 UMLS_CUI:C0002726 |
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