Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3638382019 | Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3638383012 | Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Due to | Coenzyme Q10 deficiency | false | Inferred relationship | Existential restriction modifier | 4 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Disorder of brain | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Cardiomyopathy associated with another disorder | false | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Hypertrophic cardiomyopathy | false | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Mitochondrial cytopathy | false | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Peripheral neuropathy due to metabolic disorder | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Congenital cardiovascular disorder | false | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Associated morphology | Hypertrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 2 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 3 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Occurrence | Congenital | false | Inferred relationship | Existential restriction modifier | 1 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Finding site | Myocardium structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Finding site | Peripheral nerve structure | true | Inferred relationship | Existential restriction modifier | 3 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Hypertrophic cardiomyopathy due to disorder | false | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Hypertrophic mitochondrial cardiomyopathy | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Due to | Mitochondrial cytopathy | true | Inferred relationship | Existential restriction modifier | 4 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Hereditary nephropathy | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Coenzyme Q10 deficiency | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Renal tubular disorder | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Finding site | Renal tubule structure | true | Inferred relationship | Existential restriction modifier | 5 | |
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Central nervous system complication | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Urinary complication | true | Inferred relationship | Existential restriction modifier | ||
| Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome | Is a | Metabolic renal disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR