Research of 17-alpha-hydroxylase Deficiency has been linked to Congenital Adrenal Hyperplasia, Hypertensive Disease, Hyperplasia, Adrenal Hyperplasia, Disorders Of Sex Development. The study of 17-alpha-hydroxylase Deficiency has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to 17-alpha-hydroxylase Deficiency include Secretion, Excretion, Menstruation, Aldosterone Secretion, Pathogenesis. These pathways complement our catalog of research reagents for the study of 17-alpha-hydroxylase Deficiency including antibodies and ELISA kits against 21-HYDROXYLASE, TESTICULAR FEMINIZATION, STEROID DEHYDROGENASE, AGT, NR0B1.
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on 17-alpha-hydroxylase Deficiency below!
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We have 576 products for the study of 17-alpha-hydroxylase Deficiency that can be applied to Western Blot, Flow Cytometry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.
17-alpha-hydroxylase Deficiency is also known as 17-alpha-hydroxylase deficiency, congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency, adrenal hyperplasia, congenital, type 5, congenital adrenal hyperplasia type 5.