Pfeiffer Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An acrocephalosyndactylia that has_material_basis_in mutations in the FGFR1 and FGFR2 gene which results_in premature fusion located_in skull. (Human Disease Ontology, DOID_14705)
External Link	https://www.disgenet.org/browser/0/1/0/C0220658
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Genes

8 genes associated with the disease Pfeiffer Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
FGF13	fibroblast growth factor 13
FGF2	fibroblast growth factor 2 (basic)
FGF8	fibroblast growth factor 8 (androgen-induced)
FGFR1	fibroblast growth factor receptor 1
FGFR2	fibroblast growth factor receptor 2
FGFR3	fibroblast growth factor receptor 3
RUNX2	runt-related transcription factor 2
TWIST1	twist family bHLH transcription factor 1