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Article

[Deficiency of 11beta-hydroxysteroid dehydrogenase type 2 (syndrome of apparent mineralocorticoid excess)].

Nihon rinsho. Japanese journal of clinical medicine - 28 May 2006

Mune Tomoatsu

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 16776240

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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[Deficiency of 11beta-hydroxysteroid dehydrogenase type 2 (syndrome of apparent mineralocorticoid excess)].PMID 16776240Read ↗

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[3Beta-hydroxysteroid dehydrogenase deficiency].Semantic proximity Read ↗

[A case of apparent mineralocorticoid excess caused by type 2 11 beta- hydroxysteroid dehydrogenase deficiency].Semantic proximity Read ↗

Apparent mineralocorticoid excess.Semantic proximity Read ↗

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[11 beta-hydroxysteroid-dehydrogenase: characteristics and the clinical significance of a key enzyme in cortisol metabolism].Semantic proximity Read ↗

[17beta-hydroxysteroid dehydrogenase deficiency].Semantic proximity Read ↗

Apparent mineralocorticoid excess (AME) syndrome.Semantic proximity Read ↗

[11Beta-hydroxylase deficiency].Semantic proximity Read ↗

[Importance of the 11β-hydroxysteroid dehydrogenase enzyme in clinical disorders].Semantic proximity Read ↗

[Syndrome of apparent mineralocorticoid excess caused by a deficiency of 11 beta-hydroxysteroid dehydrogenase: clinical and genetic study in a Chilean family followed for 19 years].Semantic proximity Read ↗

Human hypertension caused by mutations in the 11 beta-hydroxysteroid dehydrogenase gene: a molecular analysis of apparent mineralocorticoid excess.Semantic proximity Read ↗

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