Disease #00532

Official abbreviation 617675
Name Myopathy, mitochondrial, and ataxia, 617675 (3)
OMIM ID 617675
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MSTO1
Associated tissues -
Disease features -
Remarks -

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