Mitochondrial Oxidative Phosphorylation Disorder

Alias:
Oxphos - [oxidative Phosphorylation] Diseases
Mitochondrial Respiratory Chain Disorders
Oxphos Disease
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Oxidative Phosphorylation Disorder, also known as oxphos - [oxidative phosphorylation] diseases, is related to lactic acidosis and leigh syndrome. An important gene associated with Mitochondrial Oxidative Phosphorylation Disorder is MTFMT (Mitochondrial Methionyl-TRNA Formyltransferase). Affiliated tissues include liver and skeletal muscle, and related phenotype is Strongly decreased CFP-tsO45G cell surface transport.
Related ID:
ICD11:1204111545

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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5
24
9

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
Related Gene
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Publications
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References Literature

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