12p12.1 microdeletion syndrome
MONDO:0017781Also known as: Del(12)(p12.1), monosomy 12p12.1
0 clinical trials for this condition and its sub-types.
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Disease
(680)
Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Autosomal anomaly
(0)
Chromosome 12 disorder
(0)
Chromosome 12p deletion
(0)
Disease by etiologic mechanism
(0)
Partial deletion of chromosome 12
(0)
Syndrome caused by partial chromosomal deletion
(0)
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