Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3663537014 | Severe early-onset axonal neuropathy due to MFN2 (mitofusin 2) deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3663538016 | Severe early-onset axonal neuropathy due to MFN2 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3663539012 | Autosomal recessive Charcot-Marie-Tooth disease Ouvrier type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3663540014 | Severe early-onset axonal neuropathy due to mitofusin 2 deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3663541013 | Severe early-onset axonal neuropathy due to mitofusin 2 deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Severe early-onset axonal neuropathy due to mitofusin 2 deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Severe early-onset axonal neuropathy due to mitofusin 2 deficiency | Is a | Hereditary motor and sensory neuropathy | true | Inferred relationship | Existential restriction modifier | ||
| Severe early-onset axonal neuropathy due to mitofusin 2 deficiency | Finding site | Peripheral nervous system structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR