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1p21.3 microdeletion syndrome

Disease Summary
Associated Targets (1)
Tclin

1


Explore Associated Targets
Mondo Description 1p21.3 microdeletion syndrome is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder.
Mondo Term and Equivalent IDs
MONDO:0017405:  1p21.3 microdeletion syndrome
Orphanet:293948: 
SCTID:719600006: 
UMLS:C4304578: 
UMLS:CN203152: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found