. . . . . . . "[Steroid 11?-hydroxylase deficiency (11?-OHD), one of common cause of congenital adrenal hyperplasia (CAH), is an autosomal recessive disorder characterized by virilization, precocious pseudo-puberty, and hypertension.It is caused by CYP11B1 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:11:54+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .