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Congenital disorder of glycosylation type 1L

Also Known As:

Congenital Disorder of Glycosylation, Type IL

Networked: 2 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 1L: 2
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 1L: 2

Experts

1.	Balog, Crina I A: 1 article (03/2013)
2.	Braulke, Thomas: 1 article (03/2013)
3.	Hykollari, Alba: 1 article (03/2013)
4.	Paschinger, Katharina: 1 article (03/2013)
5.	Rendić, Dubravko: 1 article (03/2013)
6.	Wilson, Iain B H: 1 article (03/2013)
7.	Aebi, Markus: 1 article (07/2005)
8.	Clarke, Joe T R: 1 article (07/2005)
9.	Frank, Christian G: 1 article (07/2005)
10.	Griffiths, Anne: 1 article (07/2005)

Drugs and Biologics

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

1.	Polysaccharides (Glycans)IBA 03/01/2013 - "The HL241 mutant strain of the cellular slime mold Dictyostelium discoideum is a potential model for human congenital disorder of glycosylation type IL (ALG9-CDG) and has been previously predicted to possess a lower degree of modification of its N-glycans with anionic moieties than the parental wild-type. "
2.	MannosyltransferasesIBA 07/15/2005 - "We describe the second case of congenital disorder of glycosylation type IL (CDG-IL) caused by deficiency of the ALG9 a1,2 mannosyltransferase enzyme. "
3.	EnzymesIBA 07/15/2005 - "We describe the second case of congenital disorder of glycosylation type IL (CDG-IL) caused by deficiency of the ALG9 a1,2 mannosyltransferase enzyme. "