Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3314130019 | Autosomal recessive limb girdle muscular dystrophy type 2E (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3314131015 | Autosomal recessive limb girdle muscular dystrophy type 2E | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3314132010 | Limb girdle muscular dystrophy due to beta-sarcoglycan deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal recessive limb girdle muscular dystrophy type 2E | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive limb girdle muscular dystrophy type 2E | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive limb girdle muscular dystrophy type 2E | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive limb girdle muscular dystrophy type 2E | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive limb girdle muscular dystrophy type 2E | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR