Status: current, Primitive. 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 | Initial character case insensitive | SNOMED CT core |
3437355017 | Autosomal recessive limb girdle muscular dystrophy type 2J | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3437356016 | Limb-girdle muscular dystrophy 2J titin gene mutation | en | Synonym | Active | Initial character case insensitive | 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 | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive limb girdle muscular dystrophy type 2J | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2J | Clinical course | Progressive | true | Inferred relationship | Some | 2 | |
Autosomal recessive limb girdle muscular dystrophy type 2J | Is a | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
Autosomal recessive limb girdle muscular dystrophy type 2J | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Autosomal recessive limb girdle muscular dystrophy type 2J | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set