Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3311380019 | Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3311381015 | Autosomal recessive limb girdle muscular dystrophy type 2C | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3311382010 | Limb girdle muscular dystrophy due to gamma-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 2C | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Existential restriction modifier | ||
| Autosomal recessive limb girdle muscular dystrophy type 2C | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive limb girdle muscular dystrophy type 2C | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive limb girdle muscular dystrophy type 2C | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
| Autosomal recessive limb girdle muscular dystrophy type 2C | 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