Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency
MONDO:0008730A very rare form of congenital adrenal hyperplasia (CAH) characterized by glucocorticoid deficiency, hypergonadotrophic hypogonadism and severe hypokalemic hypertension.
Also known as: 17-alpha-hydroxylase/17,20-lyase deficiency, CAH due to 17-alpha-hydroxylase deficiency, combined 17-hydroxylase/17,20-lyase deficiency, 17,20-lyase deficiency, isolated, 17-Alpha-Hydroxylase deficiency, 17-Alpha-Hydroxylase/17,20-lyase deficiency, combined complete, 17-Alpha-Hydroxylase/17,20-lyase deficiency, combined partial, adrenal hyperplasia 5
3 clinical trials for this condition and its sub-types.
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Disease
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Metabolic disease
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Inherited lipid metabolism disorder
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Hereditary disease
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Endocrine system disorder
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Inborn errors of metabolism
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Congenital adrenal hyperplasia
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Adrenocortical insufficiency
(26)
Hereditary endocrine growth disease
(24)
Reproductive system disorder
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