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 |
| 3331990013 | Glycogen storage disease due to acid maltase deficiency, infantile onset | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3331991012 | Glycogenosis due to acid maltase deficiency, infantile onset | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3331992017 | Glycogenosis type II, infantile onset | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3331993010 | Pompe disease, infantile onset | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3331994016 | Glycogen storage disease type II infantile onset (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3334442014 | Glycogen storage disease type II infantile onset | 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 infantile onset | Is a | Glycogen storage disease, type II | true | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease type II infantile 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
FHIR