| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_3783) |
| External Link | http://www.omim.org/entry/303600 |
| Similar Terms | |
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1 genes associated with the coffin-lowry syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| RPS6KA3 | ribosomal protein S6 kinase, 90kDa, polypeptide 3 |