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Pituitary hormone deficiency, combined, 6

MONDO:0013518

Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the OTX2 gene.

Also known as: OTX2 combined pituitary hormone deficiencies, genetic form, combined pituitary hormone deficiencies, genetic form caused by mutation in OTX2, pituitary hormone deficiency, combined, 6, pituitary hormone deficiency, combined, type 6, CPHD6

1 clinical trial for this condition and its sub-types.

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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) Hereditary endocrine growth disease (24) Hypogonadotropic hypogonadism (18) Pituitary gland disorder (16)
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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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