Matches in DBpedia 2016-04 for { <http://wikidata.dbpedia.org/resource/Q494922> ?p ?o }
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- Q494922 subject Q6407955.
- Q494922 subject Q6902466.
- Q494922 subject Q8543555.
- Q494922 abstract "Glycogen storage disease type III is an autosomal recessive metabolic disorder and inborn error of metabolism characterized by a deficiency in glycogen debranching enzymes.It is also known as Cori's disease in honor of the 1947 Nobel laureates Carl Cori and Gerty Cori. Other names include Forbes disease in honor of clinician Gilbert Burnett Forbes (1915-2003), an American Physician who further described the features of the disorder, or limit dextrinosis, due to the limit dextrin-like structures in cytosol. Limit dextrin is the remaining polymer produced after hydrolysis of glycogen. Without glycogen debranching enzymes to further convert these branched glycogen polymers to glucose, limit dextrinosis abnormally accumulates in the cytoplasm.Glycogen is a molecule the body uses to store carbohydrate energy. Symptoms of GSD-III are caused by a deficiency of the enzyme amylo-1,6 glucosidase, or debrancher enzyme. This causes excess amounts of an abnormal glycogen to be deposited in the liver, muscles and, in some cases, the heart.".
- Q494922 icd10 "E74.0".
- Q494922 icd9 "271.0".
- Q494922 meshId "D006010".
- Q494922 omim "232400".
- Q494922 thumbnail Glycogen_storage_disease_in_liver_-_high_mag.jpg?width=300.
- Q494922 wikiPageExternalLink default.asp.
- Q494922 wikiPageWikiLink Q104053.
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- Q494922 wikiPageWikiLink Q131774.
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- Q494922 wikiPageWikiLink Q1753547.
- Q494922 wikiPageWikiLink Q1758393.
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- Q494922 wikiPageWikiLink Q191835.
- Q494922 wikiPageWikiLink Q202758.
- Q494922 wikiPageWikiLink Q204733.
- Q494922 wikiPageWikiLink Q2351083.
- Q494922 wikiPageWikiLink Q360841.
- Q494922 wikiPageWikiLink Q516389.
- Q494922 wikiPageWikiLink Q6407955.
- Q494922 wikiPageWikiLink Q6531938.
- Q494922 wikiPageWikiLink Q6902466.
- Q494922 wikiPageWikiLink Q7365.
- Q494922 wikiPageWikiLink Q78501.
- Q494922 wikiPageWikiLink Q8054.
- Q494922 wikiPageWikiLink Q847583.
- Q494922 wikiPageWikiLink Q8543555.
- Q494922 wikiPageWikiLink Q9368.
- Q494922 wikiPageWikiLink Q998.
- Q494922 icd "271".
- Q494922 icd "E74.0".
- Q494922 meshid "D006010".
- Q494922 name "Glycogen storage disease type III".
- Q494922 omim "232400".
- Q494922 type Disease.
- Q494922 type Thing.
- Q494922 type Q12136.
- Q494922 comment "Glycogen storage disease type III is an autosomal recessive metabolic disorder and inborn error of metabolism characterized by a deficiency in glycogen debranching enzymes.It is also known as Cori's disease in honor of the 1947 Nobel laureates Carl Cori and Gerty Cori.".
- Q494922 label "Glycogen storage disease type III".
- Q494922 depiction Glycogen_storage_disease_in_liver_-_high_mag.jpg.
- Q494922 name "Glycogen storage disease type III".