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 |
| 3717163013 | Rhabdoid tumour predisposition syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3717164019 | Rhabdoid tumor predisposition syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3717165018 | Rhabdoid tumor predisposition syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3717166017 | Familial rhabdoid tumor | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3717167014 | Familial rhabdoid tumour | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Rhabdoid tumor predisposition syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Rhabdoid tumor predisposition syndrome | Is a | Hereditary cancer-predisposing syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Rhabdoid tumor predisposition syndrome | Occurrence | Early childhood | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR