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Chromosome Xp21 deletion syndrome

MONDO:0010399

Also known as: Del(X)(p21), Glycerol kinase deficiency-contiguous gene syndrome, Xp21 contiguous gene deletion syndrome, Xp21 microdeletion syndrome, chromosome Xp21 deletion syndrome, complex glycerol kinase deficiency, Complex Glycerol kinase deficiency

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

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Broader categories

Disease (680) Metabolic disease (233) Hereditary disease (176) Inborn errors of metabolism (45) Human disease (14) Chromosomal disorder (12) Gonosome anomaly (6) Disease of genetic or genomic mechanism (2) Chromosome X disorder (0) Disease by developmental or physiological process (0)
Trials to join now! 2 Not yet finished but already full! 2 Completed 1
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  • Scientists dig into the mysteries of x and y chromosomes

    Knowledge-focused Completed

    This study looked at 112 people with known differences in their sex chromosomes (X and Y) to better understand how these variations affect health, especially infertility. Participants underwent physical exams, blood and urine tests, imaging, and sensory checks over about 5 days. …

    Sponsor: National Human Genome Research Institute (NHGRI) • Aim: Knowledge-focused

    Last updated Jun 27, 2026 13:07 UTC

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