Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4009747010 | Genetic susceptibility to malignant hyperthermia (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 4009748017 | Malignant hyperthermia genetic susceptibility | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 4009749013 | Genetic susceptibility to malignant hyperthermia | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Malignant hyperthermia genetic susceptibility | Is a | Genetic susceptibility to genetic disorder | true | Inferred relationship | Some | ||
| Malignant hyperthermia genetic susceptibility | Interprets | Genetic test | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Genetic susceptibility to malignant hyperthermia due to ryanodine receptor 1 gene mutation positive | Is a | True | Malignant hyperthermia genetic susceptibility | Inferred relationship | Some | |
| Genetic susceptibility to malignant hyperthermia due to calcium voltage-gated channel subunit alpha1 S gene mutation positive | Is a | True | Malignant hyperthermia genetic susceptibility | Inferred relationship | Some |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR