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3B80.0Splenomegaly in storage diseases
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01
A disease caused by storage diseases; genetically inherited metabolic disorders that result from defects in lysosomal, lipid or glycogen function, of the spleen. This disease is characterised by enlargement of the spleen. This disease may present with abdominal pain, chest pain, pallor, shortness of breath fatigue. Confirmation is through medical imaging.
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