Mitochondrial Dna Depletion Syndrome 14 (MTDPS14)

Alias:
Mtdps14
Mitochondrial Dna Depletion Syndrome 14, Cardioencephalomyopathic Type
Mitochondrial Dna Depletion Syndrome, Type 14
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Dna Depletion Syndrome 14, also known as mtdps14, is related to autosomal dominant optic atrophy and autosomal dominant optic atrophy, classic form. An important gene associated with Mitochondrial Dna Depletion Syndrome 14 is OPA1 (OPA1 Mitochondrial Dynamin Like GTPase), and among its related pathways/superpathways is Energy metabolism. Affiliated tissues include skeletal muscle and heart, and related phenotypes are sensorineural hearing impairment and hypertonia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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9
48
1

Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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