1p35.2 microdeletion syndrome
MONDO:0018697Also known as: Del(1)(p35.2), deletion 1p35.2, monosomy 1p35.2
0 clinical trials for this condition and its sub-types.
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Disease
(680)
Human disease
(14)
Chromosomal disorder
(12)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
(2)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Autosomal anomaly
(0)
Chromosome 1 disorder
(0)
Disease by developmental or physiological process
(0)
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