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Items: 2

1.

Adrenal Gland Hyperplasia III

Decreased activity of the enzyme 21-hydroxylase, associated with mutation(s) in the CYP21A2 gene. The lack of activity of this enzyme produces a type of congenital adrenal hyperplasia (CAH) and is the cause of approximately 95% of CAH. [from NCI]

MedGen UID:
424833
Concept ID:
C2936858
Congenital Abnormality
2.

Hyperandrogenism, nonclassic type, due to 21-hydroxylase deficiency

MedGen UID:
348518
Concept ID:
C1859995
Disease or Syndrome

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