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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.

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Sub-types

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

Broader categories

Disease (680) Nervous system disorder (231) Hereditary disease (176) Brain disorder (125) Central nervous system disorder (107) Endocrine system disorder (72) Hypogonadism (45) Isolated congenital growth hormone deficiency (36) Hereditary endocrine growth disease (24) Hypogonadotropic hypogonadism (18)
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  • 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

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