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- Q4127184 subject Q8221741.
- Q4127184 subject Q8364490.
- Q4127184 abstract "Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency is an uncommon form of congenital adrenal hyperplasia resulting from a defect in the gene CYP17A1, which encodes for the enzyme 17α-hydroxylase. It produces decreased synthesis of both cortisol and sex steroids, with resulting increase in mineralocorticoid production. Thus, common symptoms include mild hypocortisolism, ambiguous genitalia in genetic males or failure of the ovaries to function at puberty in genetic females, and hypertension (respectively).".
- Q4127184 thumbnail 17aOHdeficiency.svg?width=300.
- Q4127184 wikiPageExternalLink dispomim.cgi?id=202110.
- Q4127184 wikiPageWikiLink Q101065.
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- Q4127184 wikiPageWikiLink Q14859578.
- Q4127184 wikiPageWikiLink Q14905207.
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- Q4127184 wikiPageWikiLink Q8047.
- Q4127184 wikiPageWikiLink Q80726.
- Q4127184 wikiPageWikiLink Q8221741.
- Q4127184 wikiPageWikiLink Q8364490.
- Q4127184 wikiPageWikiLink Q912422.
- Q4127184 comment "Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency is an uncommon form of congenital adrenal hyperplasia resulting from a defect in the gene CYP17A1, which encodes for the enzyme 17α-hydroxylase. It produces decreased synthesis of both cortisol and sex steroids, with resulting increase in mineralocorticoid production.".
- Q4127184 label "Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency".
- Q4127184 depiction 17aOHdeficiency.svg.