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Article

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22).

Journal of medical genetics - 1 Nov 2000

Lafferty A R, Torpy D J, Stowasser M, Taymans S E, Lin J P, Huggard P, Gordon R D, Stratakis C A

Abstract excerpt

Familial hyperaldosteronism type II (FH-II) is caused by adrenocortical hyperplasia or aldosteronoma or both and is frequently transmitted in an autosomal dominant fashion. Unlike FH type I (FH-I), which results from fusion of the CYP11B1 and CYP11B2 genes, hyperaldosteronism in FH-II is not gluc...

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Source

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Identifiers

PMID: 11073536
DOI: 10.1136/jmg.37.11.831
PMCID: PMC1734468

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-11073536-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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