|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||Smith-Magenis syndrome (SMS) is a complex genetic disorder characterized by variable intellectual deficit, sleep disturbance, craniofacial and skeletal anomalies, psychiatric disorders, and speech and motor delay. (Orphanet Rare Disease Ontology, Orphanet_819)|
|Downloads & Tools|
1 genes associated with the Smith-Magenis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
|RAI1||retinoic acid induced 1|