Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3706572013 | Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3706573015 | Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3706574014 | Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3706575010 | Combined oxidative phosphorylation defect type 16 | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | Is a | Hypertrophic mitochondrial cardiomyopathy | true | Inferred relationship | Existential restriction modifier | ||
| Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | Due to | Mitochondrial cytopathy | true | Inferred relationship | Existential restriction modifier | 2 | |
| Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | Finding site | Myocardium structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | Associated morphology | Hypertrophy | true | Inferred relationship | Existential restriction modifier | 1 | |
| Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | Is a | Mitochondrial cytopathy | true | Inferred relationship | Existential restriction modifier | ||
| Infantile hypertrophic cardiomyopathy due to mitochondrial ribosomal protein L44 deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR