Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3426298018 | Retinopathy Burgess Black type | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3426299014 | Autosomal recessive bestrophinopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3426300018 | Autosomal recessive bestrophinopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal recessive bestrophinopathy | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Existential restriction modifier | ||
Autosomal recessive bestrophinopathy | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Autosomal recessive bestrophinopathy | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
Autosomal recessive bestrophinopathy | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets