ALG9-Congenital Disorder of Glycosylation (ALG9-CDG) is a rare, inherited disease that affects how the body builds sugar chains (called N-glycans) that are ...
Dr. Nadia Falah, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
Glucosyltransferase 2 deficiency is a rare, inherited condition where a small “assembly-line” step for building sugar chains on proteins does not work ...
Congenital disorder of glycosylation type 1h (CDG-Ih, also called ALG8-CDG) is a rare, inherited condition that affects the way the body adds sugar chains to ...
Carbohydrate-deficient glycoprotein syndrome type Ih (CDG-Ih)—also called ALG8-CDG—is a very rare, inherited disease that affects how the body builds sugar ...
ALG8-Congenital Disorder of Glycosylation (ALG8-CDG) is a rare, inherited disease. It happens when a child gets two faulty copies of the ALG8 gene—one from ...
Glucosyltransferase-1 deficiency is a rare, inherited metabolic condition. It happens when a gene called ALG6 does not work properly. The ALG6 gene makes an ...
Congenital disorder of glycosylation caused by mutation in ALG6 is a rare inherited disease. It happens when both copies of a gene called ALG6 do not work ...
Carbohydrate-deficient glycoprotein syndrome type Ic (ALG6-CDG) is a rare, inherited disease. It happens when a gene called ALG6 does not work properly. This ...
ALG6–Congenital Disorder of Glycosylation (ALG6-CDG, CDG-Ic) is a rare, inherited condition. It happens when both copies of a gene called ALG6 do not work ...
Mannosyltransferase-6 deficiency is a very rare, inherited condition that affects how the body builds sugar chains on proteins (a process called N-linked ...
Congenital disorders of glycosylation (CDG) are rare, inherited diseases in which the body has trouble attaching sugar chains (called glycans) to proteins and ...
Carbohydrate-deficient glycoprotein syndrome type Id is a rare inherited disease. It affects the way the body adds sugar chains to proteins. This sugar-adding ...
ALG3-CDG is a rare, inherited metabolic disease. It happens when a child receives two faulty copies of the ALG3 gene (one from each parent). The ALG3 gene ...
Mannosyltransferase 2 deficiency is a very rare, inherited condition. It happens when both copies of a gene called ALG2 do not work well. The ALG2 gene makes ...
Congenital Disorder of Glycosylation type 1i (CDG-1i) is a very rare, inherited metabolic disease. It happens because a small change (mutation) in a gene ...
Carbohydrate-deficient glycoprotein syndrome type II is a group of rare, inherited conditions where the body has trouble finishing the “sugar decorations” that ...
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