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DOID:14761 - Greig cephalopolysyndactyly syndrome
Disease Ontology 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.
Synonyms: polysyndactyly with peculiars skull shape,
Xenbase Genes : gli3
MONDO:0008287 - Greig cephalopolysyndactyly syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee