Status: retired, 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 |
51056015 | Charcot-Marie-Tooth disease, type II | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
51057012 | Hereditary sensory-motor neuropathy, type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
51058019 | Inherited neuronal peroneal muscular atrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
484605018 | Charcot-Marie-Tooth disease of neuronal type | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
484606017 | Autosomal recessive sensory neuropathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
484607014 | Dominant hereditary sensory neuropathy, type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
484608016 | Hereditary sensory and autonomic neuropathy type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
484609012 | Peroneal muscular atrophy of neuronal type | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
484610019 | Painless whitlow disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
484611015 | Hereditary sensory and autonomic neuropathy, type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
484612010 | Hereditary motor and sensory neuropathy type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
761520018 | Charcot-Marie-Tooth disease, type II (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets