Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3704558019 | Charcot-Marie-Tooth disease, pyramidal features syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3704559010 | Hereditary motor and sensory neuropathy type 5 (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3704560017 | Hereditary motor and sensory neuropathy type 5 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3873462011 | Hereditary sensory-motor neuropathy type V | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary motor and sensory neuropathy type 5 | Is a | Chronic nervous system disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary motor and sensory neuropathy type 5 | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 1 | |
| Hereditary motor and sensory neuropathy type 5 | Is a | Hereditary motor and sensory neuropathy | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary motor and sensory neuropathy type 5 | Finding site | Peripheral nervous system structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Hereditary motor and sensory neuropathy type 5 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR