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.