Smith-Magenis syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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)
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1 genes associated with the Smith-Magenis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
RAI1 retinoic acid induced 1