Chromosome 1q21.1 deletion syndrome
MONDO:00129141q21.1 microdeletion syndrome is a newly described recurrent deletion syndrome with variable clinical manifestations but without the clinical picture of thrombocytopenia - absent radius (TAR) syndrome.
Also known as: 1q21.1 microdeletion syndrome, 1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders), Del(1)(q21), chromosome 1q21.1 deletion syndrome, isolated cases, monosomy 1q21.1, 1q21.1 microdeletion, chromosome 1q21.1 deletion syndrome, 1.35-MB, chromosome 1q21.1 microdeletion syndrome
2 clinical trials for this condition and its sub-types.
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Disease
(618)
Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
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Chromosome 1 disorder
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Chromosome 1q deletion
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Disease by etiologic mechanism
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Partial deletion of chromosome 1
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Syndrome caused by partial chromosomal deletion
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