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Up to: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability · Partial monosomy of the short arm of chromosome 20
20p13 microdeletion syndrome
20p13 microdeletion syndrome is a rare chromosomal anomaly characterized by developmental delay, mild to moderate intellectual disability, epilepsy, and unspecific dysmorphic signs. High palate, delayed permanent tooth eruption, hypoplastic fingernails, clinodactyly and short fingers have also been reported.
This condition has no sub-types.