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 |
3311383017 | Autosomal recessive limb girdle muscular dystrophy type 2F (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
3311385012 | Autosomal recessive limb girdle muscular dystrophy type 2F | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3311386013 | Limb girdle muscular dystrophy due to delta-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 2F | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Existential restriction modifier | ||
Autosomal recessive limb girdle muscular dystrophy type 2F | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2F | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2F | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2F | 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