Coenzyme Q10 Deficiency, Primary, 9 (COQ10D9)

Alias:
Coq10d9
Primary Coenzyme Q10 Deficiency 9
Coenzyme Q10 Deficiency, Primary, Type 9
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Coenzyme Q10 Deficiency, Primary, 9, also known as coq10d9, is related to coenzyme q10 deficiency, primary, 6 and coenzyme q10 deficiency disease. An important gene associated with Coenzyme Q10 Deficiency, Primary, 9 is COQ5 (Coenzyme Q5, Methyltransferase), and among its related pathways/superpathways are Metabolism and Metabolism of steroids. Affiliated tissues include brain and eye, and related phenotypes are ataxia and global developmental delay
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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19
115
1

Medical Symptom

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Description
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Gene & Mutation

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MGI
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References Literature

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