Smith-Magenis Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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/proteins associated with the disease Smith-Magenis Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
RAI1 retinoic acid induced 1 2.88009