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 |
| 3717158014 | Autosomal dominant childhood-onset proximal spinal muscular atrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3717159018 | Autosomal dominant childhood-onset proximal spinal muscular atrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3717160011 | Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3717161010 | SMALED - spinal muscular atrophy, lower extremity, dominant | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3717162015 | Spinal muscular atrophy with lower extremity predominance | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant childhood-onset proximal spinal muscular atrophy | Is a | Spinal muscular atrophy | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant childhood-onset proximal spinal muscular atrophy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal dominant childhood-onset proximal spinal muscular atrophy | Finding site | Structure of nervous system | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR