- syndrome of apparent mineralocorticoid excess
- apparent mineralocorticoid excess.
Medical dictionary. 2011.
Medical dictionary. 2011.
Apparent mineralocorticoid excess syndrome — Classification and external resources OMIM 218030 DiseasesDB 12740 MeSH … Wikipedia
apparent mineralocorticoid excess — (AME) a rare autosomal recessive enzyme deficiency syndrome caused by mutation in the HSD11B2 gene (locus: 16q22), which encodes 11β hydroxysteroid dehydrogenase type 2; it is characterized by accumulation of cortisol in the kidney in spite… … Medical dictionary
Conradi–Hünermann syndrome — Conradi Hünermann syndrome Classification and external resources ICD 10 Q77.3 ICD 9 756.59 … Wikipedia
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Corticosteroid 11-beta-dehydrogenase isozyme 2 — Hydroxysteroid (11 beta) dehydrogenase 2 Identifiers Symbols HSD11B2; AME; AME1; HSD11K; HSD2; SDR9C3 External IDs … Wikipedia
Cortisol — Not to be confused with cortisone, a similar compound with a similar name, genesis, and function. Cortisol Systematic (IUPAC … Wikipedia
11β-hydroxysteroid dehydrogenase type 1 — is an NADPH dependent enzyme highly expressed in key metabolic tissues including liver, adipose tissue, and the central nervous system. In these tissues, HSD11B1 reduces cortisone to the active hormone cortisol that activates glucocorticoid… … Wikipedia
Синдром кажущегося избытка минералокортикоидов — OMIM 218030 218030 DiseasesDB 12740 12740 MeSH … Википедия
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency — Classification and external resources Deficient 21 Hydroxylase can lead to accumulation of 17 Hydroxyprogesterone ICD … Wikipedia
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency — Classification and external resources OMIM 202010 eMedicine article/117012 11β Hydroxylase deficient con … Wikipedia