Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1765959019 | Charcot-Marie-Tooth disease, type I (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
1777611019 | Charcot-Marie-Tooth disease, type I | en | Synonym | Active | Case sensitive | SNOMED CT core |
1786062015 | Hereditary sensory-motor neuropathy, type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1786063013 | Peroneal muscular atrophy of demyelinating type | en | Synonym | Active | Case insensitive | SNOMED CT core |
1786064019 | Inherited dominant hypertrophic neuropathy | en | Synonym | Active | Case insensitive | SNOMED CT core |
1786065018 | Hereditary motor and sensory neuropathy type I | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
1786066017 | Charcot-Marie-Tooth disease of demyelinating type | en | Synonym | Active | Case sensitive | SNOMED CT core |
1786067014 | HSMN, type I | en | Synonym | Active | Case sensitive | SNOMED CT core |
2966574017 | Charcot Marie Tooth disease, type 1 | en | Synonym | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Charcot-Marie-Tooth disease, type I | Is a | Charcot-Marie-Tooth disease | false | Inferred relationship | Some | ||
Charcot-Marie-Tooth disease, type I | Finding site | Peripheral nervous system structure | true | Inferred relationship | Some | 1 | |
Charcot-Marie-Tooth disease, type I | Associated morphology | Neuropathic atrophy | false | Inferred relationship | Some | 1 | |
Charcot-Marie-Tooth disease, type I | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 1 | |
Charcot-Marie-Tooth disease, type I | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 1 | |
Charcot-Marie-Tooth disease, type I | Associated morphology | Neuropathic atrophy | false | Inferred relationship | Some | 1 | |
Charcot-Marie-Tooth disease, type I | Is a | Hereditary motor and sensory neuropathy | true | Inferred relationship | Some | ||
Charcot-Marie-Tooth disease, type I | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
PMP2-related Charcot-Marie-Tooth disease type 1 | Is a | True | Charcot-Marie-Tooth disease, type I | Inferred relationship | Some | |
Charcot-Marie-Tooth disease, type IA | Is a | True | Charcot-Marie-Tooth disease, type I | Inferred relationship | Some | |
Charcot-Marie-Tooth disease, type IC | Is a | True | Charcot-Marie-Tooth disease, type I | Inferred relationship | Some | |
Charcot-Marie-Tooth disease, type IB | Is a | True | Charcot-Marie-Tooth disease, type I | Inferred relationship | Some | |
Charcot-Marie-Tooth disease type IE | Is a | True | Charcot-Marie-Tooth disease, type I | Inferred relationship | Some | |
Charcot-Marie-Tooth disease type 1D | Is a | True | Charcot-Marie-Tooth disease, type I | Inferred relationship | Some | |
Charcot-Marie-Tooth disease type 1F | Is a | True | Charcot-Marie-Tooth disease, type I | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set