Mitochondrial Complex Iv Deficiency, Nuclear Type 9 (MC4DN9)

Alias:
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 3
Mc4dn9
Cemcox3
Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency 3
Mitochondrial Complex Iv, Deficiency, Nuclear Type 9
Mitochondrial Complex Iv Deficiency Nuclear Type 9
Mitochondrial Complex Iv Deficiency, Type 9
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Complex Iv Deficiency, Nuclear Type 9, is also known as cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3. An important gene associated with Mitochondrial Complex Iv Deficiency, Nuclear Type 9 is COA5 (Cytochrome C Oxidase Assembly Factor 5). Affiliated tissues include heart, and related phenotypes are hypertrophic cardiomyopathy and cardiomyocyte mitochondrial proliferation
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
3
1

Medical Symptom

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Description
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No data available

Gene & Mutation

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No data available

Disease Model

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MGI
Related Gene
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Publications
No data available

References Literature

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IF
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