Disease table of GREIG CEPHALOPOLYSYNDACTYLY SYNDROME OMIM ID: 175700

Gene-disease associations table

GeneAssociated with GREIG CEPHALOPOLYSYNDACTYLY SYNDROME inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
GLI3ClinVar, OMIM, HUMSAVARHGNC link7p14.15174700, 174200, 241800, 146510, 175700

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