Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4650594010 | Autosomal recessive limb girdle muscular dystrophy, cardiac arrhythmia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4650596012 | Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4650597015 | Limb girdle muscular dystrophy 2X | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4650600019 | BVES-related limb girdle muscular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4650601015 | Blood vessel epicardial substance related limb girdle muscular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 4650602010 | BVES (blood vessel epicardial substance) related limb girdle muscular dystrophy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4650595011 | A rare subtype of autosomal recessive limb girdle muscular dystrophy characterised by atrioventricular block resulting in repeated syncope episodes, elevated creatine kinase serum levels and adult-onset of slowly progressive proximal limb skeletal muscle weakness and atrophy. Muscular dystrophic changes observed in muscle biopsy include diameter variability, increased central nuclei and presence of necrotic and regenerating fibres. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4650599017 | A rare subtype of autosomal recessive limb girdle muscular dystrophy characterized by atrioventricular block resulting in repeated syncope episodes, elevated creatine kinase serum levels and adult-onset of slowly progressive proximal limb skeletal muscle weakness and atrophy. Muscular dystrophic changes observed in muscle biopsy include diameter variability, increased central nuclei and presence of necrotic and regenerating fibers. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | est un(e) (attribut) | cardiopathie chronique | true | Inferred relationship | Some | ||
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | est un(e) (attribut) | Autosomal recessive muscular dystrophy with limb girdle distribution | true | Inferred relationship | Some | ||
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | est un(e) (attribut) | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | est un(e) (attribut) | Cardiac arrhythmia associated with genetic disorder (disorder) | true | Inferred relationship | Some | ||
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 2 | |
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | localisation d'une constatation (attribut) | cœur | true | Inferred relationship | Some | 3 | |
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | localisation d'une constatation (attribut) | structure de muscle squelettique | true | Inferred relationship | Some | 1 | |
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | morphologie associée (attribut) | Dystrophy (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Blood vessel epicardial substance related limb girdle muscular dystrophy (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR