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