pfeiffer syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
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2 genes associated with the pfeiffer syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2