Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2989388010 | Suspected hereditary disease | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 2989498015 | Suspected hereditary disease (situation) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Suspected hereditary disease | est un(e) (attribut) | Disease suspected (situation) | true | Inferred relationship | Some | ||
| Suspected hereditary disease | constatation associée (attribut) | maladie héréditaire | true | Inferred relationship | Some | 1 | |
| Suspected hereditary disease | nature de la relation avec la personne visée (attribut) | Subject of record (person) | true | Inferred relationship | Some | 1 | |
| Suspected hereditary disease | contexte temporel (attribut) | Current or specified time (qualifier value) | true | Inferred relationship | Some | 1 | |
| Suspected hereditary disease | contexte de la constatation (attribut) | Suspected (qualifier value) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Suspected cystic fibrosis (situation) | est un(e) (attribut) | True | Suspected hereditary disease | Inferred relationship | Some | |
| Suspected phenylketonuria (situation) | est un(e) (attribut) | True | Suspected hereditary disease | Inferred relationship | Some | |
| Suspected sickle cell disease (situation) | est un(e) (attribut) | True | Suspected hereditary disease | Inferred relationship | Some | |
| Suspected sickle cell trait (situation) | est un(e) (attribut) | True | Suspected hereditary disease | Inferred relationship | Some | |
| Suspected medium-chain acyl-coenzyme A dehydrogenase deficiency (situation) | est un(e) (attribut) | True | Suspected hereditary disease | Inferred relationship | Some |
This concept is not in any reference sets
FHIR