Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3757957016 | Congenital muscular dystrophy without intellectual disability (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3757958014 | Congenital muscular dystrophy without intellectual disability | en | Synonym | Active | Case insensitive | SNOMED CT core |
3757959018 | A rare genetic congenital muscular dystrophy due to dystroglycanopathy disorder with characteristics of a wide phenotypic spectrum which includes hypotonia and muscular weakness present at birth or early infancy, delayed or arrested motor development and normal intellectual abilities with normal (or only mild abnormalities) neuroimaging studies. Feeding difficulties, joint and spinal deformities and respiratory insufficiency may be associated. Decreased alpha-dystroglycan on immunohistochemical muscle staining and elevated serum creatine kinase are observed. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital muscular dystrophy without intellectual disability | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital muscular dystrophy without intellectual disability | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Congenital muscular dystrophy without intellectual disability | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital muscular dystrophy without intellectual disability | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
Congenital muscular dystrophy without intellectual disability | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Congenital muscular dystrophy without intellectual disability | Is a | Congenital hereditary muscular dystrophy | true | Inferred relationship | Some | ||
Congenital muscular dystrophy without intellectual disability | Is a | Chronic metabolic disorder | true | Inferred relationship | Some | ||
Congenital muscular dystrophy without intellectual disability | Clinical course | Progressive | true | Inferred relationship | Some | 2 |
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