|Dataset||CTD Gene-Disease 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/proteins associated with the disease Smith-Magenis Syndrome from the curated CTD Gene-Disease Associations dataset.
|RAI1||retinoic acid induced 1||2.88009|