hypoaldosteronism, congenital, due to cmo ii deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/610600
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Genes

1 genes associated with the hypoaldosteronism, congenital, due to cmo ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2