Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form

MONDO:0017839

The salt wasting form of classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (classical 21 OHD CAH) is characterized by virilization of the external genitalia in females, hypocortisolism, precocious pseudopuberty and renal salt loss due to aldosterone deficiency.

Also known as: classic 21-OHD CAH, salt wasting form

2 clinical trials for this condition and its sub-types, 0 tagged with Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (20)

Including sub-types (2) Tagged with Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form (0)

Trials to join now! 1 Not yet recruiting 1

New imaging tracer could shed light on adrenal cholesterol

Knowledge-focused Recruiting now

This study tests a special radioactive tracer called [18F]FNP-59 to see if it can safely and clearly show cholesterol activity in the adrenal gland using PET scans. About 24 people will take part, including healthy volunteers and those with known adrenal problems. The goal is to …

Early phase 1 • Sponsor: Benjamin Viglianti • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:02 UTC

Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form

Where it sits in the disease tree

New imaging tracer could shed light on adrenal cholesterol