Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type

Alias:
Glutaric Aciduria Type 2, Mild Type
Mad Deficiency, Mild Type
Madd, Mild Type
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type, also known as glutaric aciduria type 2, mild type, is related to acyl-coa dehydrogenase, short-chain, deficiency of and carnitine-acylcarnitine translocase deficiency. An important gene associated with Multiple Acyl-Coa Dehydrogenase Deficiency, Mild Type is ETFA (Electron Transfer Flavoprotein Subunit Alpha), and among its related pathways/superpathways are Metabolism and Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins..
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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5
19
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Medical Symptom

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Description
HPO Frequency
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No data available

Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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