Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3318734013 | Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3318735014 | Autosomal dominant limb girdle muscular dystrophy type 1G | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 755171000241114 | dystrophie musculaire des ceintures autosomique dominante type 1G (trouble) | fr | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 918311000172118 | LGMD1G - limb-girdle muscular dystrophy type 1G | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 937121000172118 | dystrophie musculaire des ceintures autosomique dominante type 1G | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3318736010 | A mild form of limb girdle muscular dystrophy that has characteristics of limb-girdle weakness, marked proximal amyotrophy and abolished myotatic reflexes, associated with progressive fingers and toes flexion limitation. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | localisation d'une constatation (attribut) | structure de muscle squelettique | true | Inferred relationship | Some | 1 | |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 2 | |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | est un(e) (attribut) | Autosomal dominant muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | localisation d'une constatation (attribut) | structure de muscle squelettique | false | Inferred relationship | Some | 2 | |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | localisation d'une constatation (attribut) | structure de muscle squelettique | false | Inferred relationship | Some | 3 | |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | morphologie associée (attribut) | Developmental abnormality | false | Inferred relationship | Some | 2 | |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
| Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | false | Inferred relationship | Some | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR