Adrenal hyperplasia, congenital type 3: A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency. More detailed information about the symptoms, causes, and treatments of Adrenal hyperplasia, congenital type 3 is available below.
See full list of 39 symptoms of Adrenal hyperplasia, congenital type 3
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Adrenal hyperplasia, congenital type 3 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Adrenal hyperplasia, congenital type 3, or a subtype of Adrenal hyperplasia, congenital type 3,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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