Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2983926014 | Hereditary neoplastic syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2988878014 | Hereditary cancer-predisposing syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 2988939011 | Hereditary cancer-predisposing syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary neoplastic syndrome | Is a | Hereditary disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| MITF (melanogenesis associated transcription factor) related melanoma and renal cell carcinoma predisposition syndrome | Is a | True | Hereditary neoplastic syndrome | Inferred relationship | Some | |
| Autosomal recessive lymphoproliferative disease | Is a | True | Hereditary neoplastic syndrome | Inferred relationship | Some |
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Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR