Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3705802011 | Autosomal dominant limb-girdle muscular dystrophy type 1H | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3705803018 | Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3705802011 | Autosomal dominant limb-girdle muscular dystrophy type 1H | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3705803018 | Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3705804012 | A subtype of autosomal dominant limb-girdle muscular dystrophy with characteristics of slowly progressive proximal muscular weakness initially affecting the lower limbs (and later involving the upper limbs), hypotrophy of upper and lower limb-girdle muscles, hyporeflexia, calf hypertrophy, and increased serum creatine kinase. There is no involvement of oculo-facial-bulbar muscles and cardiac muscle. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3438451001000111 | Gliedergürtelmuskeldystrophie, autosomal-dominante, Typ 1H | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
959101000172117 | LGMD1H - limb-girdle muscular dystrophy type 1H | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
974511000172114 | dystrophie musculaire des ceintures autosomique dominante type 1H | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
959101000172117 | LGMD1H - limb-girdle muscular dystrophy type 1H | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
974511000172114 | dystrophie musculaire des ceintures autosomique dominante type 1H | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3438451001000111 | Gliedergürtelmuskeldystrophie, autosomal-dominante, Typ 1H | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets