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 aquired subtypes [LS]. |
| ID |
http://purl.obolibrary.org/obo/DOID_9120 |
| comment |
amyloidosis has both inherited and aquired subtypes [LS]. |
| database_cross_reference |
MESH:D000686 UMLS_CUI:C0002726 ICD10CM:E85 NCI:C2868 SNOMEDCT_US_2022_09_01:154769007 ICD9CM:277.3 |
| 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. |
| 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_FlyBase_slim |
| label |
amyloidosis |
| notation |
DOID:9120 |
| prefLabel |
amyloidosis |
| subClassOf |