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Partial deletion of chromosome 1

MONDO:0016866

Also known as: partial deletion of chromosome type 1, partial monosomy of chromosome 1

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

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Sub-types

Chromosome 1q21.1 deletion syndrome (1) 1p21.3 microdeletion syndrome (0) 1p35.2 microdeletion syndrome (0) 1q44 microdeletion syndrome (0) Chromosome 1p32-p31 deletion syndrome (0) Chromosome 1p35 deletion syndrome (0) Chromosome 1p36 deletion syndrome (0) Chromosome 1q41-q42 deletion syndrome (0) Chromosome 1q deletion (0) Distal monosomy 1q (0) Partial deletion of the short arm of chromosome 1 (0)

Broader categories

Disease (680) Human disease (14) Chromosomal disorder (12) Disease of genetic or genomic mechanism (2) Autosomal anomaly (0) Chromosome 1 disorder (0) Disease by etiologic mechanism (0) Syndrome caused by partial chromosomal deletion (0)
Trials to join now! 1
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  • Can mapping rare genetic variants unlock better care for autism-related disorders?

    Knowledge-focused Recruiting now

    This international online study collects medical, behavioral, and developmental information from people with rare genetic changes that are linked to autism and other neurodevelopmental disorders. By partnering with families, researchers aim to build a detailed database to improve…

    Sponsor: Simons Searchlight • Aim: Knowledge-focused

    Last updated Jul 25, 2026 00:00 UTC

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