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- Q1947298 subject Q8543555.
- Q1947298 abstract "Glycogen storage disease type VI (GSD VI) is a type of glycogen storage disease caused by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system.It is also known as "Hers' disease", after Henri G. Hers, who characterized it in 1959.The scope of GSD VI now also includes glycogen storage disease type VIII, IX (caused by phosphorylase b kinase deficiency) and X (deficiency of protein kinase A). These were previously considered to be distinct GSD types.The incidence of GSD VI is approximately 1 case per 65,000–85,000 births, representing approximately 30% all cases of glycogen storage disease. Approximately 75% of these GSD VI cases result from the X-linked recessive forms of phosphorylase kinase deficiency. All other forms are autosomal recessive.".
- Q1947298 icd10 "E74.0".
- Q1947298 icd9 "271.0".
- Q1947298 meshId "D006013".
- Q1947298 omim "232700".
- Q1947298 thumbnail Glycogen.png?width=300.
- Q1947298 wikiPageExternalLink default.asp.
- Q1947298 wikiPageExternalLink NBK5941.
- Q1947298 wikiPageWikiLink Q105522.
- Q1947298 wikiPageWikiLink Q1079120.
- Q1947298 wikiPageWikiLink Q1123139.
- Q1947298 wikiPageWikiLink Q1362864.
- Q1947298 wikiPageWikiLink Q1421738.
- Q1947298 wikiPageWikiLink Q161249.
- Q1947298 wikiPageWikiLink Q174936.
- Q1947298 wikiPageWikiLink Q1988987.
- Q1947298 wikiPageWikiLink Q202758.
- Q1947298 wikiPageWikiLink Q281417.
- Q1947298 wikiPageWikiLink Q412061.
- Q1947298 wikiPageWikiLink Q512067.
- Q1947298 wikiPageWikiLink Q5253500.
- Q1947298 wikiPageWikiLink Q6531938.
- Q1947298 wikiPageWikiLink Q8543555.
- Q1947298 wikiPageWikiLink Q906540.
- Q1947298 icd "271".
- Q1947298 icd "E74.0".
- Q1947298 meshid "D006013".
- Q1947298 name "Glycogen storage disease type VI".
- Q1947298 omim "232700".
- Q1947298 type Disease.
- Q1947298 type Thing.
- Q1947298 type Q12136.
- Q1947298 comment "Glycogen storage disease type VI (GSD VI) is a type of glycogen storage disease caused by a deficiency in liver glycogen phosphorylase or other components of the associated phosphorylase cascade system.It is also known as "Hers' disease", after Henri G. Hers, who characterized it in 1959.The scope of GSD VI now also includes glycogen storage disease type VIII, IX (caused by phosphorylase b kinase deficiency) and X (deficiency of protein kinase A).".
- Q1947298 label "Glycogen storage disease type VI".
- Q1947298 depiction Glycogen.png.
- Q1947298 name "Glycogen storage disease type VI".