Snyder Robinson syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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1 genes/proteins associated with the disease Snyder Robinson syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SMS spermine synthase 2.88009