Disease table of MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 OMIM ID: 615228

Gene-disease associations table

GeneAssociated with MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
ATP5A1ClinVar, OMIM, HUMSAVARHGNC link18q21.12PS609060, 615228

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