1p21.3 microdeletion syndrome

MONDO:0017405

1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder.

Also known as: Del(1)p(21.3), monosomy 1p21.3

0 clinical trials for this condition and its sub-types, 0 tagged with 1p21.3 microdeletion syndrome itself.

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Part of

↑ Partial deletion of the short arm of chromosome 1 (0)

Including sub-types (0) Tagged with 1p21.3 microdeletion syndrome (0)

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