Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2989388010 | Suspected hereditary disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2989498015 | Suspected hereditary disease (situation) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Suspected hereditary disease | Is a | Disease suspected | true | Inferred relationship | Some | ||
| Suspected hereditary disease | Associated finding | Hereditary disease | true | Inferred relationship | Some | 1 | |
| Suspected hereditary disease | Subject relationship context | Subject of record | true | Inferred relationship | Some | 1 | |
| Suspected hereditary disease | Temporal context | Current or specified | true | Inferred relationship | Some | 1 | |
| Suspected hereditary disease | Finding context | Suspected | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Suspected cystic fibrosis | Is a | True | Suspected hereditary disease | Inferred relationship | Some | |
| Suspected phenylketonuria | Is a | True | Suspected hereditary disease | Inferred relationship | Some | |
| Suspected sickle cell disease | Is a | True | Suspected hereditary disease | Inferred relationship | Some | |
| Suspected sickle cell trait | Is a | True | Suspected hereditary disease | Inferred relationship | Some | |
| Suspected medium-chain acyl-coenzyme A dehydrogenase deficiency | Is a | True | Suspected hereditary disease | Inferred relationship | Some |
Reference Sets
Situation with explicit context foundation reference set
Problem/Diagnosis reference set
FHIR