Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4672936010 | Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
4672937018 | Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5399602011 | A progressive muscular dystrophy characterized by co-existence of limb-girdle weakness and diffuse joint contractures without cardiomyopathy. Patients present lower limb weakness progressing to involve also upper limbs and axial muscles and eventually leading to permanent loss of ambulation, widespread joint contractures in the limbs and sometimes the spine, and variable respiratory involvement. Morphological changes in muscle biopsies include rimmed vacuoles, increased internal nuclei, cytoplasmic bodies, and a dystrophic pattern. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5399603018 | A progressive muscular dystrophy characterised by co-existence of limb-girdle weakness and diffuse joint contractures without cardiomyopathy. Patients present lower limb weakness progressing to involve also upper limbs and axial muscles and eventually leading to permanent loss of ambulation, widespread joint contractures in the limbs and sometimes the spine, and variable respiratory involvement. Morphological changes in muscle biopsies include rimmed vacuoles, increased internal nuclei, cytoplasmic bodies, and a dystrophic pattern. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | Is a | Hereditary progressive muscular dystrophy | true | Inferred relationship | Some | ||
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 2 | |
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | Occurrence | Childhood | true | Inferred relationship | Some | 1 | |
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | Finding site | Skeletal muscle structure | true | Inferred relationship | Some | 1 | |
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | Associated morphology | Dystrophy | true | Inferred relationship | Some | 1 | |
Childhood-onset progressive contractures, limb girdle weakness, muscle dystrophy syndrome | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)