loading...| Preferred Name | amyloidosis | |
| Synonyms |
amyloid disease |
|
| Definitions |
A disease of metabolsism 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]. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_9120 |
|
| comment |
amyloidosis has both inherited and acquired subtypes [LS]. |
|
| alternative label |
amyloid disease |
|
| database_cross_reference |
SNOMEDCT_US_2023_03_01:154769007 ICD10CM:E85 ICD9CM:277.3 UMLS_CUI:C0002726 MESH:D000686 NCI:C2868 |
|
| definition |
A disease of metabolsism 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]. |
|
| has close match |
MESH:D000686 |
|
| has exact match |
MESH:D000686 |
|
| has exact synonym |
amyloid disease |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:9120 |
|
| in_subset |
http://purl.obolibrary.org/obo/doid#DO_MGI_slim |
|
| label |
amyloidosis |
|
| notation |
DOID:9120 |
|
| note |
A disease of metabolsism 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]. |
|
| preferred label |
amyloidosis |
|
| prefLabel |
amyloidosis |
|
| subClassOf |