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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 Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory