Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 126187016 | Polygenic hereditary disorder | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 126188014 | Polygenic hereditary disorder, NOS | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module |
| 816638014 | Polygenic hereditary disorder (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Polygenic hereditary disorder | Is a | Hereditary disease | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR