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 |
3450985013 | Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3450986014 | Autosomal recessive limb girdle muscular dystrophy type 2P | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5403551012 | A form of limb-girdle muscular dystrophy characterized by slowly progressive, mainly proximal, muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles, and contractures of the ankles. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403552017 | A form of limb-girdle muscular dystrophy characterised by slowly progressive, mainly proximal, muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles, and contractures of the ankles. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3450985013 | Autosomal recessive limb girdle muscular dystrophy type 2P (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3450986014 | Autosomal recessive limb girdle muscular dystrophy type 2P | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3450987017 | A form of limb-girdle muscular dystrophy with characteristics of slowly-progressive mainly proximal muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles and contractures of the ankles. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403551012 | A form of limb-girdle muscular dystrophy characterized by slowly progressive, mainly proximal, muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles, and contractures of the ankles. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403552017 | A form of limb-girdle muscular dystrophy characterised by slowly progressive, mainly proximal, muscle weakness presenting in early childhood (with difficulties walking and climbing stairs) and mild to severe intellectual disability. Additional manifestations reported include microcephaly, mild increase in thigh or calf muscles, and contractures of the ankles. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3388071001000111 | Alpha-Dystroglycan-assoziierte Gliedergürtelmuskeldystrophie R16 | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
882621000172112 | LGMD2P - limb-girdle muscular dystrophy type 2P | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
924691000172116 | dystrophie musculaire des ceintures autosomique récessive type 2P | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
882621000172112 | LGMD2P - limb-girdle muscular dystrophy type 2P | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
924691000172116 | dystrophie musculaire des ceintures autosomique récessive type 2P | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3388071001000111 | Alpha-Dystroglycan-assoziierte Gliedergürtelmuskeldystrophie R16 | 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)