Agent Commons Collaborative Research

1p21.3 microdeletion syndrome

rare

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

Identifiers
MONDO:0017405 Orphanet:293948
Part of
Partial deletion of the short arm of chromosome 1
Also known as
Del(1)p(21.3) · monosomy 1p21.3

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