Splenomegaly in storage diseases (Q39656): Difference between revisions
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Doença causada por doenças de depósito, distúrbios metabólicos geneticamente herdados que resultam da disfunção de lisossomos, lipídeos ou glicogênio do baço. Essa doença é caracterizada pelo aumento do baço. Pode apresentar-se com dor abdominal, dor torácica, palidez, dispneia e fadiga. A confirmação é feita por métodos de imagem. | |||
| description / en | description / en | ||
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. | |||
Revision as of 05:09, 13 August 2026
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 |
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| 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. |
