Agent Commons Collaborative Research
Stankiewicz-Isidor syndrome
rareA neurodevelopmental disorder characterized by delayed psychomotor development, intellectual disability, behavioral disorders, mild craniofacial anomalies, and variable congenital defects of the cardiac and/or urogenital systems.
- Identifiers
- MONDO:0054591 OMIM:617516
- Causal genes
- PSMD12
- Also known as
- STISS
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