Disease

congenital disorder of glycosylation type IId

Name: congenital disorder of glycosylation type IId
Creator: Alliance of Genome Resources
License: CC BY 4.0
Keywords: disease DOID:0070256 congenital disorder of glycosylation type IId A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the B4GALT1 gene on chromosome 9p21.1. CDG2D CDGIId CDG IId

Definition

A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the B4GALT1 gene on chromosome 9p21.1.

Synonyms

CDG IId
CDG2D

Cross References

GARD:9841
MESH:C535753

Parent Terms

autosomal recessive disease
congenital disorder of glycosylation type II

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

Gene	Species	Association	Disease Qualifier	Disease	Evidence	Based On	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page

Associated Alleles

Allele	Species	Association	Disease Qualifier	Disease	Evidence	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page

Associated Models

Model	Species	Experimental condition	Association	Disease Qualifiers	Disease	Condition Modifier	Genetic Modifier	Evidence	Source	References
No records match query. Try removing filters.

Showing 0 - 0 of 0 rows

per page