Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3120012 | Familial amyloid neuropathy, Finnish type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
705455016 | Familial amyloid neuropathy, Finnish type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial amyloid neuropathy, Finnish type | Is a | Familial amyloid polyneuropathy (disorder) | false | Inferred relationship | Some | ||
Familial amyloid neuropathy, Finnish type | Finding site | Nerve structure | false | Inferred relationship | Some | ||
Familial amyloid neuropathy, Finnish type | Associated morphology | Amyloid deposition | false | Inferred relationship | Some | 1 | |
Familial amyloid neuropathy, Finnish type | Finding site | Peripheral nervous system structure | false | Inferred relationship | Some | 1 | |
Familial amyloid neuropathy, Finnish type | Associated morphology | Amyloid deposition | false | Inferred relationship | Some | 1 | |
Familial amyloid neuropathy, Finnish type | Finding site | Peripheral nervous system structure | false | Inferred relationship | Some | 1 | |
Familial amyloid neuropathy, Finnish type | Finding site | Peripheral nerve structure | false | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Lattice corneal dystrophy (disorder) | Is a | False | Familial amyloid neuropathy, Finnish type | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
REPLACED BY association reference set (foundation metadata concept)