Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form
MONDO:0017840The simple virilizing form of classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency (classical 21 OHD CAH) is characterized by genital ambiguity and virilization of the external genitalia in females, hypocortisolism and precocious pseudopuberty without salt-wasting.
Also known as: classic 21-OHD CAH, simple virilizing form
2 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
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Hereditary endocrine growth disease
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Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
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