Isolated growth hormone deficiency type III

MONDO:0010615

Also known as: Fleisher syndrome, X-linked IGHD, X-linked isolated growth hormone deficiency, congenital IGHD type III, congenital isolated GH deficiency type III, congenital isolated growth hormone deficiency type III, isolated growth hormone deficiency type III, isolated growth hormone deficiency, type IIi, with agammaglobulinemia, X-linked recessive

1 clinical trial for this condition and its sub-types, 0 tagged with Isolated growth hormone deficiency type III itself.

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Where it sits in the disease tree

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↑ Isolated congenital growth hormone deficiency (38)

Sub-types of Isolated growth hormone deficiency type III

Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia 0 trials

Including sub-types (1) Tagged with Isolated growth hormone deficiency type III (0)

Not yet finished but already full! 1

Pituitary patients followed for years to uncover key outcomes

Knowledge-focused Ongoing

This study follows 1500 patients with pituitary gland disorders to see how they fare over time, whether treated with medication, surgery, or just monitoring. Researchers will track tumor regrowth after surgery to find clues that predict recurrence. The goal is to learn, not to te…

Sponsor: University of Alberta • Aim: Knowledge-focused

Last updated Jun 27, 2026 11:01 UTC

Isolated growth hormone deficiency type III

Where it sits in the disease tree

Pituitary patients followed for years to uncover key outcomes