Status: current. Date: 31-Jul 2019
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3756960017 | Genetic disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3756961018 | Genetic disease (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 |
| Genetic disease | Is a | Disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary disease | Is a | True | Genetic disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome | Is a | True | Genetic disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Isolated polycystic liver disease (disorder) | Is a | True | Genetic disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
This concept is not in any reference sets
FHIR