craniosynostosis Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A synostosis that results_in premature fusion located_in skull. (Human Disease Ontology, DOID_2340)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:2340
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Genes

1 genes associated with the disease craniosynostosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
BBS9 Bardet-Biedl syndrome 9 1.99917