| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| 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) |
| Similar Terms | |
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2 genes involed in the disease pfeiffer syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
