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 |
3331996019 | Glycogen storage disease type II late onset (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
3331997011 | Glycogen storage disease type II late onset | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3331998018 | Glycogen storage disease due to acid maltase deficiency, late-onset | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3331999014 | Alpha-1,4-glucosidase acid deficiency, late onset | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
3332000015 | Glycogenosis type II, late onset | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
3332001016 | Pompe disease, late onset | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Glycogen storage disease type II late onset | Is a | Glycogen storage disease, type II | true | Inferred relationship | Existential restriction modifier | ||
Glycogen storage disease type II late onset | 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