Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 293184014 | Branching-transferase deficiency glycogenosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 293185010 | Andersen disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 293186011 | Branching enzyme deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 293187019 | Glycogenosis, type 4 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 293188012 | Andersen's disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 293189016 | Glycogen storage disease type IV | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 574362013 | Branching-transferase deficiency glycogenosis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Branching-transferase deficiency glycogenosis | Is a | Glycogen storage disease | false | Inferred relationship | Existential restriction modifier | ||
| Branching-transferase deficiency glycogenosis | Finding site | Skeletal muscle structure | false | Inferred relationship | Existential restriction modifier | ||
| Branching-transferase deficiency glycogenosis | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | ||
| Branching-transferase deficiency glycogenosis | Finding site | Liver structure | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR