Mitochondrial Dna-Related Progressive External Ophthalmoplegia

Alias:
Maternally-Inherited Chronic Progressive External Ophthalmoplegia
Mtdna-Related Progressive External Ophthalmoplegia
Maternally-Inherited Cpeo
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Dna-Related Progressive External Ophthalmoplegia, also known as maternally-inherited chronic progressive external ophthalmoplegia, is related to chronic progressive external ophthalmoplegia and kearns-sayre syndrome. An important gene associated with Mitochondrial Dna-Related Progressive External Ophthalmoplegia is MT-TL2 (Mitochondrially Encoded TRNA-Leu (CUN) 2). Affiliated tissues include eye, and related phenotypes are progressive external ophthalmoplegia and muscle abnormality related to mitochondrial dysfunction
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Mit
Adolescent
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Medical Symptom

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Description
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Gene & Mutation

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Related Drugs

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Disease Model

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Name
MGI
Related Gene
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Publications
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References Literature

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