DDX41-related hematologic malignancy predisposition syndrome

Orpha code: 488647OMIM code: 616871

Definicja

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.

Disease data
Klasyfikacja

Disease

Kod ORPHA
488647
Kod OMIM
616871
Kod ICD10
C96.7
Kod ICD11
-

No additional description.

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