Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2021. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 135701000146112 | Congenital myotonia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 135711000146114 | Congenital myotonia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 712251000146114 | congenitale myotonie (aandoening) | nl | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 712261000146112 | congenitale myotonie | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| congenitale myotonie (aandoening) | Is a | Myotonic disorder | false | Inferred relationship | Some | ||
| congenitale myotonie (aandoening) | Finding site | Skeletal muscle structure | false | Inferred relationship | Some | 2 | |
| congenitale myotonie (aandoening) | Occurrence | Congenital | false | Inferred relationship | Some | 1 | |
| congenitale myotonie (aandoening) | Is a | Congenital disease (disorder) | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Steinert myotonic dystrophy syndrome | Is a | False | congenitale myotonie (aandoening) | Inferred relationship | Some | |
| Congenital myotonic dystrophy | Is a | False | congenitale myotonie (aandoening) | Inferred relationship | Some | |
| Congenital myotonia, autosomal recessive form | Is a | False | congenitale myotonie (aandoening) | Inferred relationship | Some | |
| Congenital myotonia, autosomal dominant form | Is a | False | congenitale myotonie (aandoening) | Inferred relationship | Some | |
| Myotonia congenita (disorder) | Is a | False | congenitale myotonie (aandoening) | Inferred relationship | Some | |
| Richieri Costa-da Silva syndrome | Is a | False | congenitale myotonie (aandoening) | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
SAME AS association reference set (foundation metadata concept)
FHIR