Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2017. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
138321000146110 | Familial amyloidosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
138331000146112 | Familial amyloidosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
713491000146112 | familiaire amyloïdose (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
713501000146119 | familiaire amyloïdose | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial amyloidosis (disorder) | Associated morphology | Amyloid deposition | true | Inferred relationship | Some | 1 | |
Familial amyloidosis (disorder) | Is a | Familial disease | true | Inferred relationship | Some | ||
Familial amyloidosis (disorder) | Is a | Amyloidosis | true | Inferred relationship | Some | ||
Familial amyloidosis (disorder) | Is a | Metabolic disease | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Familial amyloid polyneuropathy (disorder) | Is a | False | Familial amyloidosis (disorder) | Inferred relationship | Some | |
Danish type familial amyloid cardiomyopathy | Is a | False | Familial amyloidosis (disorder) | Inferred relationship | Some | |
Familial amyloid nephropathy with urticaria AND deafness | Is a | False | Familial amyloidosis (disorder) | Inferred relationship | Some | |
Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | False | Familial amyloidosis (disorder) | Inferred relationship | Some | |
Familial amyloid polyneuropathy with cutaneous amyloidosis (disorder) | Is a | False | Familial amyloidosis (disorder) | Inferred relationship | Some |
This concept is not in any reference sets