Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3728155011 | Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3728156012 | Retinal dystrophy with inner nuclear layer and ganglion cell anomalies | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3728157015 | Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies | Is a | Hereditary retinal dystrophy | true | Inferred relationship | Existential restriction modifier | ||
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies | Finding site | Retinal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets