Paternal 14q32.2 microdeletion syndrome
MONDO:0016780Also known as: paternal del(14)(q32.2), paternal monosomy 14q32.2
2 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
Disease
(618)
Syndromic disease
(24)
Human disease
(14)
Chromosomal disorder
(12)
Disease of genetic or genomic mechanism
(2)
Disease by body system or component
(0)
Disease by etiologic mechanism
(0)
Motor developmental delay due to 14q32.2 paternally expressed gene defect
(0)
Partial deletion of the long arm of chromosome 14
(0)
Syndrome caused by partial chromosomal deletion
(0)