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 |
3311380019 | Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311381015 | Autosomal recessive limb girdle muscular dystrophy type 2C | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311382010 | Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5401691011 | A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401692016 | A subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3311380019 | Autosomal recessive limb girdle muscular dystrophy type 2C (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311381015 | Autosomal recessive limb girdle muscular dystrophy type 2C | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311382010 | Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3311382010 | Limb girdle muscular dystrophy due to gamma-sarcoglycan deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3311384011 | Autosomal recessive limb girdle muscular dystrophy type 2C (LGMD2C) is a limb girdle muscular dystrophy with manifestations of limb-girdle weakness, calf hypertrophy, diaphragmatic weakness and variable cardiac abnormalities. Ambulation may be lost by the age 12. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401691011 | A subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401692016 | A subtype of autosomal recessive limb-girdle muscular dystrophy characterised by a childhood onset of progressive shoulder and pelvic girdle muscle weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. Mild to moderate elevated serum creatine kinase levels and positive Gowers sign are reported. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3391371001000117 | Gamma-Sarkoglykan-assoziierte Gliedergürtelmuskeldystrophie R5 | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
901541000172115 | dystrophie musculaire des ceintures autosomique récessive type 2C | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
930671000172112 | dystrophie musculaire des ceintures par déficit en gamma-sarcoglycane | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
901541000172115 | dystrophie musculaire des ceintures autosomique récessive type 2C | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
930671000172112 | dystrophie musculaire des ceintures par déficit en gamma-sarcoglycane | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3391371001000117 | Gamma-Sarkoglykan-assoziierte Gliedergürtelmuskeldystrophie R5 | 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)