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    <!-- http://evs.nci.nih.gov/ftp1/NDF-RT/NDF-RT.owl#N0000000324 -->

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        <ns2:MeSH_CUI>M0000487</ns2:MeSH_CUI>
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        <ns2:code>C834</ns2:code>
        <ns2:UMLS_CUI>C0001627</ns2:UMLS_CUI>
        <ns2:Synonym>Hyperplasia, Congenital Adrenal</ns2:Synonym>
        <ns2:Synonym>Congenital Adrenal Hyperplasia</ns2:Synonym>
        <ns2:SNOMED_CID>237751000</ns2:SNOMED_CID>
        <ns2:MeSH_Definition>A group of inherited disorders of the ADRENAL GLANDS, caused by enzyme defects in the synthesis of cortisol (HYDROCORTISONE) and/or ALDOSTERONE leading to accumulation of precursors for ANDROGENS. Depending on the hormone imbalance, congenital adrenal hyperplasia can be classified as salt-wasting, hypertensive, virilizing, or feminizing. Defects in STEROID 21-HYDROXYLASE; STEROID 11-BETA-HYDROXYLASE; STEROID 17-ALPHA-HYDROXYLASE; 3-beta-hydroxysteroid dehydrogenase (3-HYDROXYSTEROID DEHYDROGENASES); TESTOSTERONE 5-ALPHA-REDUCTASE; or steroidogenic acute regulatory protein; among others, underlie these disorders.</ns2:MeSH_Definition>
        <ns2:MeSH_Name>Adrenal Hyperplasia, Congenital</ns2:MeSH_Name>
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        <ns2:RxNorm_CUI>1023878</ns2:RxNorm_CUI>
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