Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770376014 | Primary systemic (AL fibril type) amyloidosis (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 1781591014 | Primary systemic (AL fibril type) amyloidosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 281391000052112 | primär systemisk amyloidos, AL-fibrilltyp | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| primär systemisk amyloidos, AL-fibrilltyp | Is a | Systemic amyloidosis affecting skin (disorder) | false | Inferred relationship | Some | ||
| primär systemisk amyloidos, AL-fibrilltyp | Associated morphology | Amyloid deposition | false | Inferred relationship | Some | ||
| primär systemisk amyloidos, AL-fibrilltyp | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
| primär systemisk amyloidos, AL-fibrilltyp | Associated morphology | Focal amyloid | false | Inferred relationship | Some | 1 | |
| primär systemisk amyloidos, AL-fibrilltyp | Finding site | Skin structure | false | Inferred relationship | Some | 1 | |
| primär systemisk amyloidos, AL-fibrilltyp | Associated morphology | Focal amyloid | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Amyloid light chain amyloidosis due to multiple myeloma (disorder) | Is a | False | primär systemisk amyloidos, AL-fibrilltyp | Inferred relationship | Some | |
| Primary systemic amyloidosis associated with occult plasma cell dyscrasia | Is a | False | primär systemisk amyloidos, AL-fibrilltyp | Inferred relationship | Some | |
| Macroglossia due to amyloidosis (disorder) | Is a | False | primär systemisk amyloidos, AL-fibrilltyp | Inferred relationship | Some | |
| Pseudoscleroderma due to amyloid light-chain amyloidosis | Is a | False | primär systemisk amyloidos, AL-fibrilltyp | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR