Reye Syndrome

Alias:
Reye's Syndrome
Liver Fatty Metamorphosis--Acute Encephalopathy Syndrome
Fatty Liver with Encephalopathy
Reye Encephalopathy
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Reye Syndrome, also known as reye's syndrome, is related to long-chain 3-hydroxyacyl-coa dehydrogenase deficiency and acyl-coa dehydrogenase, short-chain, deficiency of, and has symptoms including back pain, headache and pain. An important gene associated with Reye Syndrome is ACADM (Acyl-CoA Dehydrogenase Medium Chain), and among its related pathways/superpathways are Metabolism and Fatty acid metabolism. Affiliated tissues include liver and brain, and related phenotypes are liver/biliary system and homeostasis/metabolism
Related ID:
MESH:D012202
ICD11:649014905

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Infant
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19
140
3

Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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Disease Model

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MGI
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References Literature

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