Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 410733010 | Glycogen heart disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 410734016 | Generalised glycogen storage disease of infants | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 410735015 | Generalized glycogen storage disease of infants | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 667668013 | Glycogen storage disease, type II (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 2765038013 | Glycogen storage disease, type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3297533010 | Pompe's disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3297616011 | Pompe disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3331980017 | Glycogen storage disease due to acid maltase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3331981018 | Alpha-1,4-glucosidase acid deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3331982013 | Glycogenosis due to acid maltase deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3331983015 | Glycogenosis type II | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Glycogen storage disease, type II | Is a | Glycogen storage disease | true | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease, type II | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Glycogen storage disease, type II | Finding site | Skeletal muscle structure | false | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease, type II | Finding site | Liver structure | false | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease, type II | Is a | Glycogen storage disease, muscular form | false | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease, type II | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Glycogen storage disease type II infantile onset | Is a | True | Glycogen storage disease, type II | Inferred relationship | Existential restriction modifier | |
| Glycogen storage disease type II late onset | Is a | True | Glycogen storage disease, type II | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR