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 |
206429016 | Hereditary sensory-motor neuropathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
206430014 | Hereditary sensory and motor neuropathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
206431013 | Hereditary sensorimotor neuropathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
206432018 | HSMN | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
206433011 | HMSN | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
206434017 | Hereditary motor and sensory neuropathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
474337018 | Hereditary peripheral neuropathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
474338011 | CMT - Charcot-Marie-Tooth disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
474339015 | HSMN - Hereditary sensory and motor neuropathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
474340018 | HMSN - Hereditary motor and sensory neuropathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
474341019 | Charcot-Marie-Tooth disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
474342014 | Peroneal muscular atrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
732167016 | Hereditary motor and sensory neuropathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary motor and sensory neuropathy | Is a | Hereditary peripheral neuropathy | false | Inferred relationship | Existential restriction modifier | ||
Hereditary motor and sensory neuropathy | Finding site | Peripheral nervous system structure | false | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets