Skip to search formSkip to main contentSkip to account menu

17,20-Lyase Deficiency, Isolated

Known as: 17-Alpha-Hydroxylase-17,20-Lyase Deficiency, Combined Complete, 17-ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED PARTIAL, 17-Alpha-Hydroxylase-17,20-Lyase Deficiency, Combined Partial 
National Institutes of Health

Related topics

Related topics

2 relations

Broader (2)

Congenital adrenal hyperplasiaCytochrome P450

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1994
1994
Genomic Analysis of Two Siblings with 17.ALPHA.-Hydroxylase Deficiency and Hypertension.
17α-hydroxylase/17, 20-lyase deficiency is an autosomal recessive disorder, which causes mineralcorticoid hypertension. Here we… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)