Disease table of CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME OMIM ID: 610474

Gene-disease associations table

GeneAssociated with CAMPTODACTYLY, TALL STATURE, AND HEARING LOSS SYNDROME inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
FGFR3OMIM, HUMSAVARHGNC link4p16.316603956, 109800, 149730, 101400, 100800, 610474, 182000, 162900, 612247, 146000, 602849, 114500, 273300, 187600, 187601, 616482

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