|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Snyder-Robinson syndrome (SRS) is an X-linked intellectual disability syndrome, including also hypotonia, an unsteady gait, osteoporosis, kyphoscoliosis and facial asymmetry. Severe generalized psychomotor evolving to moderate to profound global intellectual disability is also observed. (Orphanet Rare Disease Ontology, Orphanet_3063)|
|Downloads & Tools|
1 genes/proteins associated with the disease Snyder Robinson syndrome from the curated CTD Gene-Disease Associations dataset.