Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3736373018 | Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
785131000241117 | maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante avec douleurs neuropathiques (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
882411000172116 | maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante avec douleurs neuropathiques | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
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 | Entire term case sensitive (core metadata concept) | 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 | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | est un(e) (attribut) | Hereditary motor and sensory neuropathy (disorder) | true | Inferred relationship | Some | ||
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | localisation d'une constatation (attribut) | structure du système nerveux périphérique | true | Inferred relationship | Some | 1 | |
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | est un(e) (attribut) | Disorder characterized by pain (disorder) | false | Inferred relationship | Some | ||
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | est un(e) (attribut) | Neuropathic pain | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets