Term Name:	congenital disorder of glycosylation Iw
Synonyms:	congenital disorder of glycosylation 1w
Definition:	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.
Ontology:	Human Disease [DOID:0080572]   ( DOID:0080572 )