| Dataset | OMIM Gene-Disease 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) |
| External Link | http://www.omim.org/entry/182290 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the smith-magenis syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| RAI1 | retinoic acid induced 1 |
