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Chromosome 18p deletion syndrome

MONDO:0007800

Monosomy 18p refers to a chromosomal disorder resulting from the deletion of all or part of the short arm of chromosome 18.

Also known as: 18p syndrome, 18p-, chromosome 18p deletion, chromosome 18p deletion syndrome, deletion 18p syndrome, monosomy type 18p, partial deletion of chromosome 18p, partial deletion of the short arm of chromosome 18

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

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Broader categories

Disease (618) Syndromic disease (24) Human disease (14) Chromosomal disorder (12) Disease of genetic or genomic mechanism (2) Chromosome 18 disorder (1) Autosomal anomaly (0) Disease by body system or component (0) Disease by etiologic mechanism (0) Partial deletion of chromosome 18 (0)
Trials to join now! 1 Not yet finished but already full! 1 Completed 1
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  • Could a simple questionnaire unlock the secrets of Kids' eating disorders?

    Knowledge-focused Completed

    This study tested a new parent questionnaire called ORALQUEST to assess feeding and eating disorders in children aged 9 months to 6 years. Researchers included 338 children with chronic conditions like heart defects or autism, as well as those with picky eating. The goal was to s…

    Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:04 UTC

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