Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Jun 2022. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5068811012 | Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5068812017 | Fatal congenital hypertrophic cardiomyopathy due to glycogenosis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 5068813010 | Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Is a | Congenital anomaly of myocardium | true | Inferred relationship | Existential restriction modifier | ||
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Is a | Glycogen storage disease | true | Inferred relationship | Existential restriction modifier | ||
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Is a | Developmental hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Is a | Hypertrophic cardiomyopathy due to glycogen storage disease | true | Inferred relationship | Existential restriction modifier | ||
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Due to | Glycogen storage disease | true | Inferred relationship | Existential restriction modifier | 2 | |
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Finding site | Myocardium structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Associated morphology | Hypertrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | Pathological process | Pathological developmental process | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR