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 |
3442512013 | Congenital muscular dystrophy Paradas type (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3442513015 | Congenital muscular dystrophy Paradas type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3442514014 | Congenital myopathy Paradas type | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
5403469018 | A rare congenital muscular dystrophy characterized by early onset of hypotonia, delayed motor development, and variably progressive generalized muscle weakness. Predominant involvement of pelvic and neck flexor muscles has been reported, as well as early involvement of hamstrings and medial gastrocnemius visible on muscle MRI. Serum creatine kinase levels are markedly elevated (in some cases already from early childhood). Muscle biopsy shows absence of dysferlin. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5403470017 | A rare congenital muscular dystrophy characterised by early onset of hypotonia, delayed motor development, and variably progressive generalised muscle weakness. Predominant involvement of pelvic and neck flexor muscles has been reported, as well as early involvement of hamstrings and medial gastrocnemius visible on muscle MRI. Serum creatine kinase levels are markedly elevated (in some cases already from early childhood). Muscle biopsy shows absence of dysferlin. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital muscular dystrophy Paradas type (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital muscular dystrophy Paradas type (disorder) | Is a | Congenital muscular dystrophy | false | Inferred relationship | Some | ||
Congenital muscular dystrophy Paradas type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
Congenital muscular dystrophy Paradas type (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 2 | |
Congenital muscular dystrophy Paradas type (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Congenital muscular dystrophy Paradas type (disorder) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 3 | |
Congenital muscular dystrophy Paradas type (disorder) | Associated morphology | Dystrophy | false | Inferred relationship | Some | 2 | |
Congenital muscular dystrophy Paradas type (disorder) | Associated morphology | Developmental anomaly | false | Inferred relationship | Some | 3 | |
Congenital muscular dystrophy Paradas type (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital muscular dystrophy Paradas type (disorder) | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Congenital muscular dystrophy Paradas type (disorder) | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Congenital muscular dystrophy Paradas type (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital muscular dystrophy Paradas type (disorder) | Is a | Congenital hereditary muscular dystrophy | true | Inferred relationship | Some | ||
Congenital muscular dystrophy Paradas type (disorder) | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)