Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4635369015 | Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 4635370019 | Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4635371015 | Congenital muscular dystrophy Davignon Chauveau type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | Is a | Congenital hereditary muscular dystrophy | true | Inferred relationship | Existential restriction modifier | ||
| Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | Clinical course | Progressive | true | Inferred relationship | Existential restriction modifier | 2 | |
| Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | Finding site | Skeletal muscle structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Congenital muscular dystrophy, respiratory failure, skin abnormalities, joint hyperlaxity syndrome | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets