congenital disorder of glycosylation Ij

Summary

DOID:0080562 - congenital disorder of glycosylation Ij

Disease Ontology Definition:A congenital disorder of glycosylation I that is characterized by hypotonia, intractable seizures, developmental delay, microcephaly and severe fetal hypokinesia and has_material_basis_in homozygous or compound heterozygous mutation in the DPAGT1 gene, which encodes UDP-GlcNAc:dolichyl-phosphate N-acetylglucosamine phosphotransferase, on chromosome 11q23.

Synonyms: Congenital disorder of glycosylation 1j

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: dpagt1

MIM:

MIM:608093 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J

MIM:608093 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), congenital disorder of glycosylation type I (is_a)