congenital disorder of glycosylation Iaa

Term ID

DOID:0080553

Synonyms

congenital disorder of glycosylation 1aa

Definition

A congenital disorder of glycosylation I that is characterized by fibroblasts with reduced dolichol profiles and enhanced accumulation of free cholesterol and has_material_basis_in homozygous mutation in the NUS1 gene on chromosome 6q22. https://www.ncbi.nlm.nih.gov/pubmed/25066056

References

OMIM:617082

Ontology

Human Disease ( DOID:0080553 )

Relationships

is a type of: autosomal recessive disease congenital disorder of glycosylation type I

autosomal recessive disease congenital disorder of glycosylation type I Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations