- Glucocorticoid deficiency 1
Glucocorticoid deficiency 1 is an
adrenocortical failure characterized by low levels of plasmacortisol despite high levels of plasmaACTH .External links
*
Wikimedia Foundation. 2010.
Glucocorticoid deficiency 1 is an
External links
*
Wikimedia Foundation. 2010.
Glucocorticoid — Chemical structure of cortisol, a glucocorticoid … Wikipedia
Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency — Classification and external resources OMIM 202110 DiseasesDB 1841 … Wikipedia
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency — Classification and external resources Deficient 21 Hydroxylase can lead to accumulation of 17 Hydroxyprogesterone ICD … Wikipedia
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Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency — Classification and external resources Cortisol ICD 10 E … Wikipedia
17-beta-hydroxysteroid dehydrogenase deficiency — Classification and external resources OMIM 264300 DiseasesDB 32638 17 beta hydroxysteroid dehydrogenase III deficiency is a r … Wikipedia
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Mevalonate kinase deficiency — Classification and external resources A patient with mevalonate kinase deficiency at the age of 21 months, displaying characteristic craniofacial features. OMIM … Wikipedia
Allgrove syndrome — glucocorticoid deficiency with achalasia and alacrima; inherited as an autosomal recessive trait; called also achalasia addisonian s., addisonian achalasia s., and triple A s … Medical dictionary
Lipoid congenital adrenal hyperplasia — is an uncommon form of CAH resulting from defects in the earliest stages of adrenal cortisol synthesis: the transport of cholesterol into the mitochondria of the cells of the adrenal cortex and the conversion to pregnenolone. Lipoid CAH causes… … Wikipedia