| 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) |
| External Link | http://www.omim.org/entry/101600 |
| Similar Terms | |
| Downloads & Tools |
2 genes associated with the pfeiffer syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
