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- Q9081107 subject Q6500135.
- Q9081107 subject Q6853484.
- Q9081107 subject Q8636419.
- Q9081107 abstract "Pearson syndrome is a mitochondrial disease characterized by sideroblastic anemia and exocrine pancreas dysfunction. Other clinical features are failure to thrive, pancreatic fibrosis with insulin-dependent diabetes and exocrine pancreatic deficiency, muscle and neurologic impairment, and, frequently, early death. It is usually fatal in infancy. The few patients who survive into adulthood often develop symptoms of Kearns-Sayre syndrome.It is caused by a deletion in mitochondrial DNA. Pearson syndrome is very rare, less than hundred cases have been reported in medical literature worldwide.The syndrome was first described by pediatric hematologist and oncologist Howard Pearson in 1979; the deletions causing it were discovered a decade later.".
- Q9081107 omim "557000".
- Q9081107 wikiPageExternalLink mt-overview.
- Q9081107 wikiPageExternalLink index.html.
- Q9081107 wikiPageWikiLink Q124407.
- Q9081107 wikiPageWikiLink Q1497481.
- Q9081107 wikiPageWikiLink Q2605012.
- Q9081107 wikiPageWikiLink Q2610084.
- Q9081107 wikiPageWikiLink Q27075.
- Q9081107 wikiPageWikiLink Q4.
- Q9081107 wikiPageWikiLink Q605709.
- Q9081107 wikiPageWikiLink Q6500135.
- Q9081107 wikiPageWikiLink Q656732.
- Q9081107 wikiPageWikiLink Q6853484.
- Q9081107 wikiPageWikiLink Q7365.
- Q9081107 wikiPageWikiLink Q754845.
- Q9081107 wikiPageWikiLink Q83042.
- Q9081107 wikiPageWikiLink Q8636419.
- Q9081107 wikiPageWikiLink Q935710.
- Q9081107 wikiPageWikiLink Q9618.
- Q9081107 name "Pearson syndrome".
- Q9081107 omim "557000".
- Q9081107 type Disease.
- Q9081107 type Thing.
- Q9081107 type Q12136.
- Q9081107 comment "Pearson syndrome is a mitochondrial disease characterized by sideroblastic anemia and exocrine pancreas dysfunction. Other clinical features are failure to thrive, pancreatic fibrosis with insulin-dependent diabetes and exocrine pancreatic deficiency, muscle and neurologic impairment, and, frequently, early death. It is usually fatal in infancy. The few patients who survive into adulthood often develop symptoms of Kearns-Sayre syndrome.It is caused by a deletion in mitochondrial DNA.".
- Q9081107 label "Pearson syndrome".
- Q9081107 name "Pearson syndrome".