_:vb50941968 . _:vb50941967 . "GARD:3307"^^ . _:vb50941968 . . "A syndromic X-linked intellectual disability that is characterized by a tall, marfanoid stature, distinct facial dysmorphism and behavioral problems and that has_material_basis_in hemizygous mutation in the MED12 gene on chromosome Xq13. Opitz-Kaveggia syndrome is an allelic disorder with an overlapping phenotype."^^ . . _:vb50941967 . "syndromic X-linked intellectual disorder Lujan-Fryns-type"@en . _:vb50941968 . _:vb50941967 . "disease_ontology"^^ . _:vb50941968 . "DOID:0080985"^^ . "ORDO:776"^^ . _:vb50941968 . _:vb50941967 . _:vb50941967 . "OMIM:309520"^^ . . .