Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1765959019 | Charcot-Marie-Tooth disease, type I (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
1777611019 | Charcot-Marie-Tooth disease, type I | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
1786062015 | Hereditary sensory-motor neuropathy, type I | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
1786063013 | Peroneal muscular atrophy of demyelinating type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
1786064019 | Inherited dominant hypertrophic neuropathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
1786065018 | Hereditary motor and sensory neuropathy type I | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
1786066017 | Charcot-Marie-Tooth disease of demyelinating type | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
1786067014 | HSMN, type I | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
2966574017 | Charcot Marie Tooth disease, type 1 | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
This concept is not in any reference sets