Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 345067019 | Bulbospinal neuronopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 345068012 | Kennedy syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 345069016 | X-linked bulbospinal atrophy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 345070015 | Bulbospinal muscular atrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 618035018 | Bulbospinal neuronopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Bulbospinal neuronopathy | Is a | Spinal muscular atrophy | true | Inferred relationship | Existential restriction modifier | ||
| Bulbospinal neuronopathy | Associated morphology | Degeneration | false | Inferred relationship | Existential restriction modifier | 2 | |
| Bulbospinal neuronopathy | Finding site | Motor neuron | false | Inferred relationship | Existential restriction modifier | ||
| Bulbospinal neuronopathy | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 1 | |
| Bulbospinal neuronopathy | Is a | X-linked hereditary disease | false | Inferred relationship | Existential restriction modifier | ||
| Bulbospinal neuronopathy | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR