"ORDO:370921"^^ . "DOID:0080572"^^ . "OMIM:615596"^^ . _:vb50941220 . _:vb50941220 . _:vb50941220 . "disease_ontology"^^ . _:vb50941220 . _:vb50941219 . . . "A congenital disorder of glycosylation I that is characterized by developmental delay, intellectual disability, failure to thrive, hypotonia and seizures and has_material_basis_in homozygous mutation in the STT3A gene on chromosome 11q24."^^ . "congenital disorder of glycosylation 1w"@en . . "congenital disorder of glycosylation Iw"^^ . . _:vb50941219 . _:vb50941220 . _:vb50941219 . _:vb50941219 . _:vb50941219 .