20p13 microdeletion syndrome

MONDO:0017780

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.

Also known as: 20p subtelomeric deletion syndrome, Del(20)(p13), monosomy 20p13

0 clinical trials for this condition and its sub-types, 0 tagged with 20p13 microdeletion syndrome itself.

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↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ Partial monosomy of the short arm of chromosome 20 (0)

Including sub-types (0) Tagged with 20p13 microdeletion syndrome (0)

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