Status: current. Date: 31-Jul 2020
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3944369015 | Glycogen storage disease due to liver and muscle glycogen phosphorylase kinase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3977970010 | Glycogen storage disease type IXB (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3977971014 | Glycogen storage disease type IXB | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Glycogen storage disease type IXB (disorder) | Is a | Glycogen phosphorylase kinase deficiency | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Glycogen storage disease type IXB (disorder) | Occurrence | Congenital | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Glycogen storage disease type IXB (disorder) | Finding site | Liver structure | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR