Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3736372011 | Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3736373018 | Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3736374012 | A rare subtype of autosomal dominant intermediate Charcot-Marie-Tooth disease with characteristics of debilitating neuropathic pain associated with mild distal symmetrical lower limb sensory loss and mild or absent motor dysfunction. Patients typically manifest with burning, aching, shooting or throbbing pain and intermittent paresthesia in toes, heels and ankles. | en | Definition | Active | Case sensitive | SNOMED CT core |
3736375013 | A rare subtype of autosomal dominant intermediate Charcot-Marie-Tooth disease with characteristics of debilitating neuropathic pain associated with mild distal symmetrical lower limb sensory loss and mild or absent motor dysfunction. Patients typically manifest with burning, aching, shooting or throbbing pain and intermittent paraesthesia in toes, heels and ankles. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | Is a | Hereditary motor and sensory neuropathy | true | Inferred relationship | Some | ||
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | Finding site | Peripheral nervous system structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | Is a | Disorder characterised by pain | false | Inferred relationship | Some | ||
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | Is a | Neuropathic pain | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set