Choline Deficiency Disease

Alias:
Choline Deficiency
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Choline Deficiency Disease, also known as choline deficiency, is related to metabolic dysfunction-associated steatotic liver disease and hyperhomocysteinemia. An important gene associated with Choline Deficiency Disease is PEMT (Phosphatidylethanolamine N-Methyltransferase), and among its related pathways/superpathways are Metabolism and Regulation of expression of SLITs and ROBOs. The drugs Choline and Gastrointestinal Agents have been mentioned in the context of this disorder. Affiliated tissues include liver and brain, and related phenotypes are homeostasis/metabolism and liver/biliary system
Related ID:
MESH:D002796
ICD11:1231437224

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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23
209
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Medical Symptom

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Gene & Mutation

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References Literature

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