Disease #00141

Official abbreviation MTATP6
Name ATP SYNTHASE 6;;MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1, INCLUDED
OMIM ID 516060
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes , MT-ATP6
Associated tissues -
Disease features -
Remarks -

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