Disease table of COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I OMIM ID: 613790

Gene-disease associations table

GeneAssociated with COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE I inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
C8AClinVar, OMIMHGNC link1p32.21613790

Download the disease annotation in CSV format