mitochondrial dna depletion syndrome, encephalomyopathic form, with methylmalonic aciduria, autosomal recessive

Preferred Label : mitochondrial dna depletion syndrome, encephalomyopathic form, with methylmalonic aciduria, autosomal recessive;

MeSH note : mutations in SUCLA2;

Details

Origin ID

C567624;

UMLS CUI

C3501372;

DO Cross reference
- mitochondrial DNA depletion syndrome 5 [DO Concept]
MeSH term(s) associated for indexing
- metabolism, inborn errors [MeSH Descriptor]
- mitochondrial myopathies [MeSH Descriptor]
Record concept(s)
- mitochondrial dna depletion syndrome, encephalomyopathic form, with methylmalonic aciduria, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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