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Summary Literature (2)
OMIM:175700 - GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS


Xenbase Genes: gli3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008287 - Greig cephalopolysyndactyly syndrome

Disease Ontology (DO):
DOID:14761 - Greig cephalopolysyndactyly syndrome