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Summary Literature (2)
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

Referenced OMIM:
OMIM:175700 - GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : gli3

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): acrocephalosyndactylia (is_a), autosomal dominant disease (is_a)


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Version: 4.14.0
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