Status: current. Date: 31-Aug 2022
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5089667015 | Hereditary metabolic disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5089668013 | Hereditary metabolic 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 |
| Hereditary metabolic disease | Is a | Hereditary disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Hereditary metabolic disease | Is a | Metabolic disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| FTH1-related iron overload | Is a | True | Hereditary metabolic disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Citrin deficiency (disorder) | Is a | True | Hereditary metabolic disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | |
| Inborn error of metabolism | Is a | True | Hereditary metabolic disease | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly |
This concept is not in any reference sets
FHIR