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3p25.3 microdeletion syndrome

Disease Summary
Associated Targets (0)

Explore Associated Targets
Mondo Description 3p25.3 microdeletion syndrome is a rare chromosomal anomaly characterized by intellectual disability, epilepsy or EEG abnormalities, poor speech, ataxia, and stereotypic hand movements.
Mondo Term and Equivalent IDs
MONDO:0018564:  3p25.3 microdeletion syndrome
Orphanet:435638: 
UMLS:CN237571: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found