Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1766148016 | Amyloid polyneuropathy type I (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
1777779015 | Amyloid polyneuropathy type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2477007017 | Familial amyloid neuropathy, Andrade type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2477008010 | Hereditary amyloid polyneuropathy Portuguese type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2477009019 | Familial amyloid polyneuropathy, 30 Met-for-Val | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2477010012 | Familial amyloid neuropathy, Portuguese type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2477011011 | Hereditary neuropathic amyloidosis, type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2477012016 | Portuguese polyneuritic amyloidosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
2477013014 | Swedish type amyloid polyneuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
2477014015 | Amyloidosis, type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2477015019 | Andrade type amyloid polyneuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
2477016018 | Andrade syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
2477017010 | Corino de Andrade paramyloidosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
2477018017 | Wohlwill-Corino Andrade syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2477019013 | Portuguese type amyloid polyneuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
2477020019 | Japanese type amyloid polyneuropathy | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Amyloid polyneuropathy type I | Finding site | Peripheral nerve structure | true | Inferred relationship | Some | 1 | |
Amyloid polyneuropathy type I | Is a | Familial amyloid polyneuropathy | true | Inferred relationship | Some | ||
Amyloid polyneuropathy type I | Associated morphology | Amyloid deposition | false | Inferred relationship | Some | 1 | |
Amyloid polyneuropathy type I | Finding site | Nerve structure | false | Inferred relationship | Some | ||
Amyloid polyneuropathy type I | Finding site | Peripheral nervous system structure | false | Inferred relationship | Some | 1 | |
Amyloid polyneuropathy type I | Associated morphology | Amyloid deposition | true | Inferred relationship | Some | 1 | |
Amyloid polyneuropathy type I | Finding site | Peripheral nervous system structure | false | Inferred relationship | Some | 1 | |
Amyloid polyneuropathy type I | Finding site | Peripheral nerve structure | false | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Swedish type amyloid polyneuropathy | Is a | False | Amyloid polyneuropathy type I | Inferred relationship | Some | |
Portuguese type amyloid polyneuropathy | Is a | False | Amyloid polyneuropathy type I | Inferred relationship | Some | |
Andrade type amyloid polyneuropathy | Is a | False | Amyloid polyneuropathy type I | Inferred relationship | Some | |
Japanese type amyloid polyneuropathy | Is a | False | Amyloid polyneuropathy type I | Inferred relationship | Some | |
Jewish type amyloid polyneuropathy | Is a | False | Amyloid polyneuropathy type I | Inferred relationship | Some | |
Familial amyloid polyneuropathy, Jewish type | Is a | False | Amyloid polyneuropathy type I | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set