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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

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

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Brain disorder (110) Central nervous system disorder (97) Endocrine system disorder (61) Hypogonadism (41) Hereditary endocrine growth disease (23) Hypogonadotropic hypogonadism (15) Human disease (14)
Trials to join now! 4 Not yet finished but already full! 4 Completed 1
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  • Researchers measure breathing, strength, and quality of life in hospitalized endocrine patients

    Knowledge-focused Completed

    This completed observational study at Uşak University examined 150 adults hospitalized in the endocrinology department. Researchers measured breathing, muscle strength, pain, fatigue, sleep quality, physical activity, balance, and nerve function. The goal was to better understand…

    Sponsor: Uşak University • Aim: Knowledge-focused

    Last updated Jun 27, 2026 12:30 UTC

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