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Summary Literature (0)
DOID:0080559 - congenital disorder of glycosylation Ig

Disease Ontology Definition:A congenital disorder of glycosylation I that is characterized by facial dysmorphism (prominent forehead, large ears, thin upper lip), generalized hypotonia, feeding difficulties, moderate to severe developmental delay, progressive microcephaly, frequent upper respiratory tract infections due to impaired immunity with decreased immunoglobulin levels, and decreased coagulation factors and has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding dolichyl-P-mannose:Man-7-GlcNAc-2-PP-dolichyl-alpha-6-mannosyltransferase on chromosome 22q13.

Synonyms: ALG12-congenital disorder of glycosylation, congenital disorder of glycosylation 1g,

Xenbase Genes : alg12


OMIM:
OMIM:607143 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ig; CDG1G

Other Model Organisms: AGR, 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)