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Disease Ontology Browser
Greig cephalopolysyndactyly syndrome (DOID:14761)
Alliance: disease page
Synonyms: polysyndactyly with peculiars skull shape
Alt IDs: OMIM:175700, DOID:9251, MESH:C537300, NCI:C35255, UMLS_CUI:C0265306
Definition: An acrocephalosyndactylia that has_material_basis_in mutation in the GLI3 gene which results_in abnormal development located_in limb, located_in head, located_in face.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory