Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3311383017 | Autosomal recessive limb girdle muscular dystrophy type 2F (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311385012 | Autosomal recessive limb girdle muscular dystrophy type 2F | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311386013 | Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401693014 | A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuro-psychomotor development is usually normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401694015 | A subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuro-psychomotor development is usually normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3311383017 | Autosomal recessive limb girdle muscular dystrophy type 2F (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311385012 | Autosomal recessive limb girdle muscular dystrophy type 2F | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311386013 | Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311386013 | Limb girdle muscular dystrophy due to delta-sarcoglycan deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3311387016 | Autosomal recessive limb-girdle muscular dystrophy type 2F (LGMD2F) is a limb-girdle muscular dystrophy with manifestations of limb-girdle weakness, cardiomyopathy and respiratory impairment. LGMD2F is caused by a deficit of a sarcoglycan protein and therefore belongs to a group of disorders named sarcoglycanopathy. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401693014 | A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuro-psychomotor development is usually normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401694015 | A subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a variable age of onset of progressive weakness and wasting of the proximal skeletal muscles of the shoulder and pelvic girdles, frequently associated with progressive respiratory muscle impairment and cardiomyopathy. Calf hypertrophy, muscle cramps and elevated serum creatine kinase levels are also observed. Neuro-psychomotor development is usually normal. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3387211001000113 | Delta-Sarkoglykan-assoziierte Gliedergürtelmuskeldystrophie R6 | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
922361000172112 | delta-sarcoglycanopathie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
962191000172114 | dystrophie musculaire des ceintures autosomique récessive type 2F | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
922361000172112 | delta-sarcoglycanopathie | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
962191000172114 | dystrophie musculaire des ceintures autosomique récessive type 2F | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3387211001000113 | Delta-Sarkoglykan-assoziierte Gliedergürtelmuskeldystrophie R6 | 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)