Disease table of MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARING LOSS, AND DEVELOPMENTAL DELAY OMIM ID: 613076

Gene-disease associations table

GeneAssociated with MYOPATHY, MITOCHONDRIAL PROGRESSIVE, WITH CONGENITAL CATARACT, HEARING LOSS, AND DEVELOPMENTAL DELAY inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
GFERClinVar, OMIM, HUMSAVARHGNC link16p13.31613076

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