Congenital disorder of glycosylation type 1G

Also Known As:

Congenital Disorder of Glycosylation, Type IG

Networked: 4 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Carbohydrate Metabolism
      - Congenital Disorders of Glycosylation: 570
        Congenital disorder of glycosylation type 1G: 4
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Carbohydrate Metabolism
      - Congenital Disorders of Glycosylation: 570
        Congenital disorder of glycosylation type 1G: 4

Related Diseases

1.	Metabolic Diseases (Metabolic Disease)

Experts

1.	Baráth, Peter: 1 article (11/2021)
2.	Bellová, Jana: 1 article (11/2021)
3.	Brucknerová, Ingrid: 1 article (11/2021)
4.	Brucknerová, Jana: 1 article (11/2021)
5.	Bzdúch, Vladimír: 1 article (11/2021)
6.	Hlavatá, Anna: 1 article (11/2021)
7.	Hrčková, Gabriela: 1 article (11/2021)
8.	Lekka, Dimitra-Evanthia: 1 article (11/2021)
9.	Mc Cullough, Alexandra: 1 article (11/2021)
10.	Mucha, Ján: 1 article (11/2021)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Congenital disorder of glycosylation type 1G:

1.	MannosyltransferasesIBA 10/01/2002 - "Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig." 11/01/2021 - "Congenital disorder of glycosylation type Ig (ALG12-CDG) is a rare inherited metabolic disease caused by a defect in alpha-mannosyltransferase 8, encoded by the ALG12 gene (22q13.33). "
2.	Proteins (Proteins, Gene)FDA Link 01/01/2014 - "Congenital Disorder of Glycosylation type Ig (ALG12-CDG) is part of a group of autosomal recessive conditions caused by deficiency of proteins involved in the assembly of dolichol-oligosaccharides used for protein N-glycosylation. "
3.	OligosaccharidesIBA 01/01/2014 - "Congenital Disorder of Glycosylation type Ig (ALG12-CDG) is part of a group of autosomal recessive conditions caused by deficiency of proteins involved in the assembly of dolichol-oligosaccharides used for protein N-glycosylation. "
4.	Indicators and Reagents (Reagents)IBA 08/01/2003 - "Band 3 alteration might serve as an additional indicator (some serum N-glycoproteins of hepatic origin are also indicative) of the congenital disorder of glycosylation type Ig."
5.	Glycoproteins (Glycoprotein)IBA 08/01/2003 - "Band 3 alteration might serve as an additional indicator (some serum N-glycoproteins of hepatic origin are also indicative) of the congenital disorder of glycosylation type Ig."
6.	DolicholsIBA 01/01/2014 - "Congenital Disorder of Glycosylation type Ig (ALG12-CDG) is part of a group of autosomal recessive conditions caused by deficiency of proteins involved in the assembly of dolichol-oligosaccharides used for protein N-glycosylation. "
7.	AnionsIBA 08/01/2003 - "A description is provided of the clinical presentation in an infant of the recently described congenital disorder of glycosylation type Ig, and the changes affecting glycosylation of red cell membrane band 3, the anion exchanger. "