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Disease Ontology Browser
Pfeiffer syndrome (DOID:14705)
Alliance: disease page
Synonyms: acrocephalosyndactylia type V
Alt IDs: OMIM:101600, MESH:D000168, NCI:C99100, UMLS_CUI:C0220658
Definition: An acrocephalosyndactylia that has_material_basis_in mutations in the FGFR1 and FGFR2 gene which results_in premature fusion located_in skull.

Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory