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Results 1 - 10 of 38 for hypercellular
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  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 
    ... accounts for about 1 percent of congenital adrenal hyperplasia cases. It is estimated to occur in 1 ... hydroxylase deficiency 17-alpha-hydroxylase-deficient congenital adrenal hyperplasia Adrenal hyperplasia V Combined 17 alpha-hydroxylase/17, ...
    https://medlineplus.gov/...-alpha-hydroxylase-17-20-lyase-deficiency - Genetics
  4. 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
  5. 21-hydroxylase deficiency 
    ... 95 percent of all cases of congenital adrenal hyperplasia. Mutations in the CYP21A2 gene cause 21-hydroxylase ... and symptoms of the condition. CAH1 Congenital adrenal hyperplasia 1 Congenital adrenal hyperplasia due to 21 hydroxylase ...
    https://medlineplus.gov/genetics/condition/21-hydroxylase-deficiency - Genetics
  6. Cytochrome P450 oxidoreductase 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. Rabson-Mendenhall syndrome 
    ... and symptoms of the condition. Mendenhall syndrome Pineal hyperplasia and diabetes mellitus syndrome Pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities RMS ...
    https://medlineplus.gov/.../condition/rabson-mendenhall-syndrome - Genetics
  8. Bartter syndrome 
    ... signs and symptoms of the condition. Aldosteronism with hyperplasia of the adrenal cortex Bartter disease Bartter's syndrome Juxtaglomerular hyperplasia with secondary aldosteronism Genetic Testing Registry: Antenatal Bartter ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics
  9. 3-beta-hydroxysteroid dehydrogenase deficiency 
    ... 3β-HSD deficiency 3β-HSD deficiency congenital adrenal hyperplasia 3β-hydroxysteroid dehydrogenase deficiency Type II 3β-hydroxysteroid ... Registry: 3 beta-Hydroxysteroid dehydrogenase deficiency Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency National ...
    https://medlineplus.gov/...a-hydroxysteroid-dehydrogenase-deficiency - Genetics
  10. 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
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