congenital disorder of glycosylation Ia

Summary

DOID:0080552 - congenital disorder of glycosylation Ia

Disease Ontology Definition:A congenital disorder of glycosylation I that is characterized by a severe encephalopathy with axial hypotonia, abnormal eye movement, pronounced psychomotor retardation, peripheral neuropathy, cerebellar hypoplasia, and retinitis pigmentosa and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding phosphomannomutase-2 on chromosome 16p13.

Synonyms: congenital disorder of glycosylation 1a, PMM2-congenital disorder of glycosylation

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

: pmm2

MIM:

MIM:212065 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A

MIM:212065 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ia; CDG1A

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)