Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3323619011 | Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3323620017 | Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3323621018 | Glycogen storage disease type 15 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3323622013 | Glycogen storage disease type XV | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3323623015 | Glycogenosis with severe cardiomyopathy due to glycogenin deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | Is a | Glycogen storage disease | true | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR