Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4673845019 | Glycogen storage disease due to aldolase A deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 4673846018 | Glycogen storage disease due to aldolase A deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4673848017 | Glycogen storage disease type 12 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4673849013 | Glycogen storage disease type XII | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4673850013 | Glycogenosis type 12 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4673852017 | Glycogenosis due to aldolase A deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4673853010 | Glycogenosis type XII | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Glycogen storage disease due to aldolase A deficiency | Is a | Glycogen storage disease | true | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease due to aldolase A deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Glycogen storage disease due to aldolase A 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