Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4634833013 | DDX41-related hematologic malignancy predisposition syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
4634834019 | DEAD-box helicase 41-related hematologic malignancy predisposition syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
4634835018 | DDX41-related haematologic malignancy predisposition syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
4634836017 | DEAD-box helicase 41-related hematologic malignancy predisposition syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
4634837014 | DEAD-box helicase 41-related haematologic malignancy predisposition syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
4634838016 | A rare inherited cancer-predisposing syndrome characterised by adult onset of haematologic malignancies mainly affecting the myeloid lineage (such as myelodysplastic syndrome and/or acute myeloid leukaemia), less frequently lymphoid malignancies. Some patients have been reported to develop granulomatous or immune disorders (including sarcoidosis, systemic lupus erythematosus, asthma, eczema, or juvenile arthritis) before or in the absence of haematologic malignancies. | en | Definition | Active | Case sensitive | SNOMED CT core |
4634839012 | A rare inherited cancer-predisposing syndrome characterized by adult onset of hematologic malignancies mainly affecting the myeloid lineage (such as myelodysplastic syndrome and/or acute myeloid leukemia), less frequently lymphoid malignancies. Some patients have been reported to develop granulomatous or immune disorders (including sarcoidosis, systemic lupus erythematosus, asthma, eczema, or juvenile arthritis) before or in the absence of hematologic malignancies. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
DDX41-related haematologic malignancy predisposition syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
DDX41-related haematologic malignancy predisposition syndrome | Is a | Hereditary neoplastic syndrome | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set