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- Q5883885 subject Q15127406.
- Q5883885 subject Q6902466.
- Q5883885 subject Q7215483.
- Q5883885 abstract "Holocarboxylase synthetase deficiency is an inherited metabolic disorder in which the body is unable to use the vitamin biotin effectively. This disorder is classified as a multiple carboxylase deficiency, a group of disorders characterized by impaired activity of certain enzymes that depend on biotin. Symptoms are very similar to biotinidase deficiency and treatment – large doses of biotin – is also the same.".
- Q5883885 meshId "D028922".
- Q5883885 omim "253270".
- Q5883885 thumbnail Biotin_structure.svg?width=300.
- Q5883885 wikiPageExternalLink ghr.nlm.nih.gov.
- Q5883885 wikiPageWikiLink Q11358.
- Q5883885 wikiPageWikiLink Q11367.
- Q5883885 wikiPageWikiLink Q15127406.
- Q5883885 wikiPageWikiLink Q15637420.
- Q5883885 wikiPageWikiLink Q159557.
- Q5883885 wikiPageWikiLink Q178694.
- Q5883885 wikiPageWikiLink Q181354.
- Q5883885 wikiPageWikiLink Q181409.
- Q5883885 wikiPageWikiLink Q183206.
- Q5883885 wikiPageWikiLink Q2351083.
- Q5883885 wikiPageWikiLink Q246809.
- Q5883885 wikiPageWikiLink Q2697787.
- Q5883885 wikiPageWikiLink Q34956.
- Q5883885 wikiPageWikiLink Q42918.
- Q5883885 wikiPageWikiLink Q4691924.
- Q5883885 wikiPageWikiLink Q6279182.
- Q5883885 wikiPageWikiLink Q6531938.
- Q5883885 wikiPageWikiLink Q653197.
- Q5883885 wikiPageWikiLink Q6902466.
- Q5883885 wikiPageWikiLink Q6934914.
- Q5883885 wikiPageWikiLink Q7187.
- Q5883885 wikiPageWikiLink Q7215483.
- Q5883885 wikiPageWikiLink Q776026.
- Q5883885 wikiPageWikiLink Q8047.
- Q5883885 wikiPageWikiLink Q8054.
- Q5883885 wikiPageWikiLink Q8495.
- Q5883885 wikiPageWikiLink Q9004493.
- Q5883885 wikiPageWikiLink Q9368.
- Q5883885 meshid "D028922".
- Q5883885 name "Holocarboxylase synthetase deficiency".
- Q5883885 omim "253270".
- Q5883885 type Disease.
- Q5883885 type Thing.
- Q5883885 type Q12136.
- Q5883885 comment "Holocarboxylase synthetase deficiency is an inherited metabolic disorder in which the body is unable to use the vitamin biotin effectively. This disorder is classified as a multiple carboxylase deficiency, a group of disorders characterized by impaired activity of certain enzymes that depend on biotin. Symptoms are very similar to biotinidase deficiency and treatment – large doses of biotin – is also the same.".
- Q5883885 label "Holocarboxylase synthetase deficiency".
- Q5883885 depiction Biotin_structure.svg.
- Q5883885 name "Holocarboxylase synthetase deficiency".