Status: current. Date: 31-Jan 2002
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 69728015 | Hereditary retinal dystrophy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 69729011 | Hereditary retinal dystrophy, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 778627018 | Hereditary retinal dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary retinal dystrophy | Is a | Hereditary disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Hereditary retinal dystrophy | Is a | Disorder of body system | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Hereditary retinal dystrophy | Finding site | Body system structure | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Retinohepatoendocrinologic syndrome (disorder) | Is a | True | Hereditary retinal dystrophy | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
This concept is not in any reference sets
FHIR