(Q26492817)
English
mitochondrial DNA depletion syndrome 5
Human disease
- Mitochondrial dna depletion syndrome, encephalomyopathic form with methylmalonic aciduria, autosomal recessive
- Mitochondrial encephalomyopathy aminoacidopathy
- MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA); MTDPS5
- mtDNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
- MITOCHONDRIAL DNA DEPLETION SYNDROME 5 (ENCEPHALOMYOPATHIC WITH OR WITHOUT METHYLMALONIC ACIDURIA)
- Booth-Haworth-Dilling syndrome
- Mitochondrial encephalomyopathy-aminoacidopathy syndrome
- Encephalomyopathy
- MTDPS5
- mitochondrial DNA depletion syndrome type 5
- succinate-CoA ligase deficiency
- Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With or Without Methylmalonic Aciduria, Autosomal Recessive, Sucla2-Related
Statements
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Identifiers
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