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 |
3437354018 | Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3437355017 | Autosomal recessive limb girdle muscular dystrophy type 2J | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3437356016 | Limb-girdle muscular dystrophy 2J titin gene mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5403368010 | A form of limb-girdle muscular dystrophy that usually has a childhood onset (but can range from the first to third decade of life) of severe progressive proximal weakness, eventually involving the distal muscles. Some patients may remain ambulatory but most are wheelchair dependant 20 years after onset. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3437354018 | Autosomal recessive limb girdle muscular dystrophy type 2J (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3437355017 | Autosomal recessive limb girdle muscular dystrophy type 2J | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3437356016 | Limb-girdle muscular dystrophy 2J titin gene mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3437357013 | A form of limb-girdle muscular dystrophy that usually has a childhood onset (but can range from the first to third decade of life) of severe progressive proximal weakness, eventually involving the distal muscles. Some patients may remain ambulatory but most are wheelchair dependant 20 years after onset. Caused by homozygous mutation in the titin gene (TTN). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403368010 | A form of limb-girdle muscular dystrophy that usually has a childhood onset (but can range from the first to third decade of life) of severe progressive proximal weakness, eventually involving the distal muscles. Some patients may remain ambulatory but most are wheelchair dependant 20 years after onset. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3412681001000113 | Titin-assoziierte Gliedergürtelmuskeldystrophie R10 | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
877601000172112 | dystrophie musculaire des ceintures autosomique récessive type 2J | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
878541000172114 | LGMD2J - limb-girdle muscular dystrophy type 2J | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
877601000172112 | dystrophie musculaire des ceintures autosomique récessive type 2J | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
878541000172114 | LGMD2J - limb-girdle muscular dystrophy type 2J | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3412681001000113 | Titin-assoziierte Gliedergürtelmuskeldystrophie R10 | 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)