Disease table of MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3 OMIM ID: 614053

Gene-disease associations table

GeneAssociated with MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3 inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
ATP5EClinVar, OMIM, HUMSAVARHGNC link20q13.321614053

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