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 |
3450992015 | Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3450993013 | Autosomal recessive limb girdle muscular dystrophy type 2Q | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5403553010 | A form of limb-girdle muscular dystrophy characterized by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403554016 | A form of limb-girdle muscular dystrophy characterised by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3450992015 | Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3450993013 | Autosomal recessive limb girdle muscular dystrophy type 2Q | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3450994019 | A form of limb-girdle muscular dystrophy with characteristics of proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403553010 | A form of limb-girdle muscular dystrophy characterized by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403554016 | A form of limb-girdle muscular dystrophy characterised by proximal muscle weakness presenting in early childhood (with occasional falls and difficulties in climbing stairs) and a progressive course resulting in loss of ambulation in early adulthood. Muscle atrophy and multiple contractures have also been reported in rare cases. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3443601001000119 | Plectin-assoziierte Gliedergürtelmuskeldystrophie R17 | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
901721000172118 | LGMD2Q - limb-girdle muscular dystrophy type 2Q | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
971581000172119 | dystrophie musculaire des ceintures autosomique récessive type 2Q | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
901721000172118 | LGMD2Q - limb-girdle muscular dystrophy type 2Q | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
971581000172119 | dystrophie musculaire des ceintures autosomique récessive type 2Q | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3443601001000119 | Plectin-assoziierte Gliedergürtelmuskeldystrophie R17 | 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 |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)