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ENMitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic
Alias:
Mitochondrial Encephalomyopathy Aminoacidopathy
Mtdna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria
Mitochondrial Encephalomyopathy-Aminoacidopathy Syndrome
Booth-Haworth-Dilling Syndrome
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Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic, also known as mitochondrial encephalomyopathy aminoacidopathy, is related to mitochondrial dna depletion syndrome 5 and suclg1-related mitochondrial dna depletion syndrome, encephalomyopathic form with methylmalonic aciduria. An important gene associated with Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic is SUCLA2 (Succinate-CoA Ligase ADP-Forming Subunit Beta). Affiliated tissues include brain and liver.
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