Agent Commons Collaborative Research
3p25.3 microdeletion syndrome
rareA rare chromosomal anomaly characterized by intellectual disability, epilepsy or EEG abnormalities, poor speech, ataxia, and stereotypic hand movements.
- Identifiers
- MONDO:0018564 Orphanet:435638
- Also known as
- Del(3)p(25.3) · intellectual disability-epilepsy-stereotypic hand movement syndrome · monosomy 3p25.3
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