Splenomegaly in storage diseases (Q39656)
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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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3B80.0 |
||
| English | Splenomegaly in storage diseases |
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. |
Statements
CID11:3B80.0
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