Status: current. Date: 31-Jan 2002
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 179087019 | Familial disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 189977011 | Familial disease, NOS | en | Synonym (core metadata concept) | Inactive | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 635166017 | Familial 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 |
| Familial disease | Is a | Disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial porphyria cutanea tarda | Is a | True | Familial disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Familial hypercholanemia (disorder) | Is a | True | Familial disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Familial arthrogryposis-cholestatic hepatorenal syndrome | Is a | True | Familial disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
This concept is not in any reference sets
FHIR