Mitochondrial Dna Depletion Syndrome 12a , Autosomal Dominant (MTDPS12A)

Alias:
Mtdps12a
Mitochondrial Dna Depletion Syndrome 12a, Cardiomyopathic Type, Autosomal Dominant
Mitochondrial Dna Depletion Syndrome 12a, Cardiomyopathic Type
Mitochondrial Dna Depletion Syndrome 12a Autosomal Dominant
Mitochondrial Dna Depletion Syndrome 12a Ad
Mi Dna Depletion Syndrome 12a Ad
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mitochondrial Dna Depletion Syndrome 12a , Autosomal Dominant, is also known as mtdps12a. An important gene associated with Mitochondrial Dna Depletion Syndrome 12a , Autosomal Dominant is SLC25A4 (Solute Carrier Family 25 Member 4). Related phenotypes are increased csf lactate and lactic acidosis
Related ID:

Basic Information

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

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
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Gene & Mutation

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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