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Congenital disorder of glycosylation type I
- ... disorder of glycosylation (ALG12-CDG, also known as congenital disorder of glycosylation type Ig) is an inherited disorder with varying signs ... of the condition. ALG12-CDG CDG Ig CDG1G Congenital disorder of glycosylation type 1G Congenital disorder of glycosylation type Ig Genetic ...
- ... disorder of glycosylation (ALG6-CDG, also known as congenital disorder of glycosylation type Ic) is an inherited condition that affects many ... type V CDG syndrome type Ic CDG1C CDGIc Congenital disorder of glycosylation type Ic Glucosyltransferase 1 deficiency Genetic Testing Registry: ALG6- ...
- ... disorder of glycosylation (PMM2-CDG, also known as congenital disorder of glycosylation type Ia) is an inherited condition that affects many ... glycoprotein syndrome type Ia CDG Ia CDG1a CDGS1a Congenital disorder of glycosylation type Ia Jaeken syndrome Phosphomannomutase 2 deficiency PMM deficiency ...
- ... disorder of glycosylation (SRD5A3-CDG, formerly known as congenital disorder of glycosylation type Iq) is an inherited condition that causes neurological ...
- ... disorder of glycosylation (COG5-CDG, formerly known as congenital disorder of glycosylation type IIi) is an inherited condition that causes neurological ...
- ... disorder of glycosylation (SLC35A2-CDG, formerly known as congenital disorder of glycosylation type IIm) is an inherited condition that causes neurological ...
- ... disorder of glycosylation (ALG1-CDG, also known as congenital disorder of glycosylation type Ik) is an inherited disorder with varying signs ... Carbohydrate deficient glycoprotein syndrome type Ik CDG1K CDGIk Congenital disorder of glycosylation type 1K ... Genetic Testing Registry: ALG1- ...
- ... disorder of glycosylation (DOLK-CDG, formerly known as congenital disorder of glycosylation type Im) is an inherited condition that often affects ... show signs and symptoms of the condition. CDG1M Congenital disorder of glycosylation, type Im DK1 deficiency Dolichol kinase deficiency DOLK-CDG ...
- ... Durand G, Oriol R, Codogno P, Moore SE. Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl- ... Aebi M, Hennet T. ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg. Hum Mol Genet. 2002 Sep 15;11( ...
- ... disorder of glycosylation (ALG6-CDG, also known as congenital disorder of glycosylation type Ic). This condition typically leads to developmental delay, ...