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1172625004: DEAD-box helicase 41-related hematologic malignancy predisposition syndrome (disorder)


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


0 descendants.

Expanded Value Set


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

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