Pfeiffer syndrome Gene Set

Dataset ClinVar Gene-Phenotype 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)
External Link http://www.omim.org/entry/101600
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Genes

1 genes associated with the Pfeiffer syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2