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Results 1 - 10 of 20 for Adrenal hyperplasia
  1. Primary macronodular adrenal hyperplasia 
    Primary macronodular adrenal hyperplasia (PMAH) is a disorder characterized by multiple lumps (nodules) in the adrenal glands, which are small hormone-producing ...
    https://medlineplus.gov/.../primary-macronodular-adrenal-hyperplasia - Genetics
  2. Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency 
    Congenital adrenal hyperplasia (CAH) due to 11-beta-hydroxylase deficiency is one of a group of disorders (collectively called congenital adrenal hyperplasia) that ...
    https://medlineplus.gov/...sia-due-to-11-beta-hydroxylase-deficiency - Genetics
  3. 17 alpha-hydroxylase/17,20-lyase deficiency 
    ... of a group of disorders, known as congenital adrenal hyperplasias, that impair hormone production and disrupt sexual development ... deficiency accounts for about 1 percent of congenital adrenal hyperplasia cases. It is estimated to occur in 1 ...
    https://medlineplus.gov/...-alpha-hydroxylase-17-20-lyase-deficiency - Genetics
  4. CYP21A2 gene 
    ... cytochrome P450, subfamily XXIA (steroid 21-hydroxylase, congenital adrenal hyperplasia), polypeptide 2 Cytosteroid 21-Monooxygenase P450c21B steroid 21- ...
    https://medlineplus.gov/genetics/gene/cyp21a2 - Genetics
  5. 21-hydroxylase deficiency 
    ... of a group of disorders known as congenital adrenal hyperplasias that impair hormone production and disrupt sexual development. ... about 95 percent of all cases of congenital adrenal hyperplasia. Mutations in the CYP21A2 gene cause 21-hydroxylase ...
    https://medlineplus.gov/genetics/condition/21-hydroxylase-deficiency - Genetics
  6. Cytochrome P450 oxidoreductase deficiency 
    ... deficiency of 17-hydroxylase and 21-hydroxylase Congenital adrenal hyperplasia due to apparent combined p450c17 and p450c21 deficiency POR deficiency PORD Genetic Testing Registry: Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Antley-Bixler ...
    https://medlineplus.gov/...cytochrome-p450-oxidoreductase-deficiency - Genetics
  7. 3-beta-hydroxysteroid dehydrogenase deficiency 
    ... of a group of disorders known as congenital adrenal hyperplasias that impair hormone production and disrupt sexual development ... deficiency 3β-HSD deficiency 3β-HSD deficiency congenital adrenal hyperplasia 3β-hydroxysteroid dehydrogenase deficiency Type II 3β-hydroxysteroid ...
    https://medlineplus.gov/...a-hydroxysteroid-dehydrogenase-deficiency - Genetics
  8. CYP17A1 gene 
    ... cytochrome P450, subfamily XVII (steroid 17-alpha-hydroxylase), adrenal hyperplasia cytochrome P450-C17 cytochrome P450c17 P450C17 S17AH steroid ...
    https://medlineplus.gov/genetics/gene/cyp17a1 - Genetics
  9. ARMC5 gene 
    ... have been identified in people with primary macronodular adrenal hyperplasia (PMAH), a disorder that causes multiple lumps (nodules) ... mutations are a frequent cause of primary macronodular adrenal Hyperplasia. J Clin Endocrinol Metab. 2014 Aug;99(8): ...
    https://medlineplus.gov/genetics/gene/armc5 - Genetics
  10. HSD3B2 gene 
    ... type II HSD3B HSDB Tests of HSD3B2 PubMed ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 ... respectively, nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2002 Jun;87(6): ...
    https://medlineplus.gov/genetics/gene/hsd3b2 - Genetics
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