Disease table of ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY OMIM ID: 202110

Gene-disease associations table

GeneAssociated with ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
CYP17A1ClinVar, OMIM, HUMSAVARHGNC link10q24.321202110

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