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Results 1 - 10 of 20 for hyperplastic
  1. CYP21A2 gene 
    ... P450, subfamily XXIA (steroid 21-hydroxylase, congenital adrenal hyperplasia), polypeptide 2 Cytosteroid 21-Monooxygenase P450c21B steroid 21- ... steroid 21-monooxygenase Tests of CYP21A2 PubMed ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY NCBI Gene ...
    https://medlineplus.gov/genetics/gene/cyp21a2 - Genetics
  2. CYP17A1 gene 
    ... P450, subfamily XVII (steroid 17-alpha-hydroxylase), adrenal hyperplasia cytochrome P450-C17 cytochrome P450c17 P450C17 S17AH steroid ...
    https://medlineplus.gov/genetics/gene/cyp17a1 - Genetics
  3. ARMC5 gene 
    ... been identified in people with primary macronodular adrenal hyperplasia (PMAH), a disorder that causes multiple lumps (nodules) ... each kidney. These nodules cause adrenal gland enlargement (hyperplasia) and result in production of higher-than-normal ...
    https://medlineplus.gov/genetics/gene/armc5 - Genetics
  4. HSD3B2 gene 
    ... II HSD3B HSDB Tests of HSD3B2 PubMed ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 3-BETA-HYDROXYSTEROID DEHYDROGENASE 2 ... nonclassic and classic 3beta-HSD deficiency congenital adrenal hyperplasia. J Clin Endocrinol Metab. 2002 Jun;87(6): ...
    https://medlineplus.gov/genetics/gene/hsd3b2 - Genetics
  5. CYP11B1 gene 
    ... gene have been found to cause congenital adrenal hyperplasia (CAH) due to 11-beta-hydroxylase deficiency, a ... New MI. Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia. Trends Endocrinol Metab. 2008 Apr;19(3):96- ...
    https://medlineplus.gov/genetics/gene/cyp11b1 - Genetics
  6. GNAS gene 
    ... been identified in people with primary macronodular adrenal hyperplasia (PMAH), a disorder that causes multiple lumps (nodules) ... each kidney. These nodules cause adrenal gland enlargement (hyperplasia) and result in production of higher-than-normal ...
    https://medlineplus.gov/genetics/gene/gnas - Genetics
  7. PIK3CA gene 
    ... overgrowth of tissues. These conditions include hemimegalencephaly; fibroadipose hyperplasia; and a condition called congenital lipomatous overgrowth, vascular ...
    https://medlineplus.gov/genetics/gene/pik3ca - Genetics
  8. NDP gene 
    ... This condition can result in vision loss. Persistent hyperplastic primary vitreous (PHPV) is another retinal disorder that ... back of the eye and the lens. Persistent hyperplastic primary vitreous can cause vision loss through retinal ...
    https://medlineplus.gov/genetics/gene/ndp - Genetics
  9. TSHR gene 
    ... called nonautoimmune congenital hyperthyroidism (or sporadic toxic thyroid hyperplasia). Onset of hyperthyroidism that begins in childhood or ... nonautoimmune autosomal dominant hyperthyroidism (or hereditary toxic thyroid hyperplasia). Sometimes gene mutations are acquired during a person' ...
    https://medlineplus.gov/genetics/gene/tshr - Genetics
  10. GPR101 gene 
    ... and symptoms of the condition result from enlargement (hyperplasia) of the gland or development of a noncancerous ... extra GPR101 protein results in pituitary adenoma or hyperplasia or the release of excess growth hormone. More ...
    https://medlineplus.gov/genetics/gene/gpr101 - Genetics
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