Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3451009012 | Autosomal recessive limb girdle muscular dystrophy type 2N (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3451010019 | Autosomal recessive limb girdle muscular dystrophy type 2N | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5403557011 | A form of limb-girdle muscular dystrophy characterized by proximal weakness (manifesting as slowness in running) presenting in infancy, along with calf hypertrophy, mild lordosis, scapular winging and normal intelligence (or mild intellectual disability). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403558018 | A form of limb-girdle muscular dystrophy characterised by proximal weakness (manifesting as slowness in running) presenting in infancy, along with calf hypertrophy, mild lordosis, scapular winging and normal intelligence (or mild intellectual disability). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive limb girdle muscular dystrophy type 2N (disorder) | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal recessive limb girdle muscular dystrophy type 2N (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2N (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2N (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2N (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)