Disease #00655

Official abbreviation 500015
Name Mitochondrial complex v (atp synthase) deficiency, mitochondrial type 1
OMIM ID 500015
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MT-ATP6
Associated tissues -
Disease features -
Remarks -

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