Status: current, Primitive. Date: 31-Jan 2006. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2574361014 | Danon disease (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
2577707016 | Danon disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
4634468019 | Glycogenosis due to LAMP-2 deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4634469010 | Lysosomal glycogen storage disease with normal acid maltase activity | en | Synonym | Active | Case insensitive | SNOMED CT core |
4634470011 | Glycogen storage disease due to LAMP-2 deficiency | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Danon disease | Is a | X-linked recessive hereditary disease | true | Inferred relationship | Some | ||
Danon disease | Is a | Cardiomyopathy | true | Inferred relationship | Some | ||
Danon disease | Is a | X-linked hereditary disease | false | Inferred relationship | Some | ||
Danon disease | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Danon disease | Is a | Multisystem disorder | false | Inferred relationship | Some | ||
Danon disease | Is a | Glycogen storage disease | true | Inferred relationship | Some | ||
Danon disease | Finding site | Myocardium structure | true | Inferred relationship | Some | 2 | |
Danon disease | Occurrence | Congenital | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set