Disease table of ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY OMIM ID: 201910

Gene-disease associations table

GeneAssociated with ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
CYP21A2ClinVar, OMIM, HUMSAVARHGNC link6p21.331201910

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