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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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  • Massive study aims to unlock secrets of rare chromosome 18 disorders

    Knowledge-focused Recruiting now

    This study is gathering medical and educational information from up to 4,000 people with chromosome 18 abnormalities and their families. The goal is to better understand these rare conditions and provide better resources and care. Participants must be at least one year old and in…

    Sponsor: The University of Texas Health Science Center at San Antonio • Aim: Knowledge-focused

    Last updated Jun 27, 2026 08:08 UTC

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