loading...| Preferred Name |
淀粉样变性 / Amyloidosis |
| Definitions |
Amyloidosis is a vast group of diseases defined by the presence of insoluble protein deposits in tissues. Its diagnosis is based on histological findings. Amyloidoses are classified according to clinical signs and biochemical type of amyloid protein involved. Most amyloidoses are multisystemic, 'generalized' or 'diffuse'. There are a few forms of localized amylosis. The most frequent forms are AL amyloidosis (immunoglobulins), AA (inflammatory), and ATTR (transthyretin accumulation). |
| ID |
http://purl.bmicc.cn/ontology/ICD11CN/5D00 |
| Coded_Elsewhere |
Monoclonal immunoglobulin deposition disease (2A83.5) |
| definition |
Amyloidosis is a vast group of diseases defined by the presence of insoluble protein deposits in tissues. Its diagnosis is based on histological findings. Amyloidoses are classified according to clinical signs and biochemical type of amyloid protein involved. Most amyloidoses are multisystemic, 'generalized' or 'diffuse'. There are a few forms of localized amylosis. The most frequent forms are AL amyloidosis (immunoglobulins), AA (inflammatory), and ATTR (transthyretin accumulation). |
| exclusions |
Dementia due to Alzheimer disease (6D80) |
| hasDbXref | |
| label |
淀粉样变性 / Amyloidosis |
| mappingRelation | |
| notation |
5D00 |
| prefixIRI |
ICD11CN:D00 |
| prefLabel |
淀粉样变性 / Amyloidosis |
| subClassOf |