Familial hyperaldosteronism type III

MONDO:0013359

Familial hyperaldosteronism type III (FH-III) is a rare heritable form of primary aldosteronism (PA) that is characterized by early-onset severe hypertension, non glucocorticoid-remediable hyperaldosteronism, overproduction of 18-oxocortisol and 18-hydroxycortisol, and profound hypokalemia.

Also known as: FH-III, FH3, familial hyperaldosteronism type 3, FH 3, FH III, HALD3, hyperaldosteronism, familial, type 3, hyperaldosteronism, familial, type III

8 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Endocrine system disorder (61) Hyperaldosteronism (44) Primary aldosteronism (39) Human disease (14) Adrenal gland disorder (8) Disease of genetic or genomic mechanism (2) Adrenal gland hyperfunction (1) Adrenal cortex disorder (0)

Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 1 Completed 1

Tiny trial to see if a dye helps adrenal surgery

Knowledge-focused Not yet recruiting

This study will look at 12 people having surgery to remove an adrenal gland (adrenalectomy) using robotic or laparoscopic methods. Some surgeries will use a green dye called Indocyanine Green (ICG) to help the surgeon see better, while others will not. The main goal is to track c…

Sponsor: University of Roma La Sapienza • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:32 UTC

Familial hyperaldosteronism type III

Broader categories

Tiny trial to see if a dye helps adrenal surgery