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- Q5044061 subject Q6853484.
- Q5044061 subject Q6902466.
- Q5044061 subject Q8444063.
- Q5044061 abstract "Carnitine-acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long-chain fatty acids into energy, particularly during periods without food. Carnitine, a natural substance acquired mostly through the diet, is used by cells to process fats and produce energy. People with this disorder have a faulty enzyme that prevents long-chain fatty acids from being transported into the innermost part of the mitochondria for processing.".
- Q5044061 omim "212138".
- Q5044061 thumbnail Autorecessive.svg?width=300.
- Q5044061 wikiPageExternalLink miracle-mollyjanes-world-first-story-of-survival.
- Q5044061 wikiPageExternalLink ghr.nlm.nih.gov.
- Q5044061 wikiPageWikiLink Q1362864.
- Q5044061 wikiPageWikiLink Q1425030.
- Q5044061 wikiPageWikiLink Q161801.
- Q5044061 wikiPageWikiLink Q1640868.
- Q5044061 wikiPageWikiLink Q170744.
- Q5044061 wikiPageWikiLink Q17855239.
- Q5044061 wikiPageWikiLink Q186380.
- Q5044061 wikiPageWikiLink Q189331.
- Q5044061 wikiPageWikiLink Q202758.
- Q5044061 wikiPageWikiLink Q2033861.
- Q5044061 wikiPageWikiLink Q2351083.
- Q5044061 wikiPageWikiLink Q243309.
- Q5044061 wikiPageWikiLink Q257319.
- Q5044061 wikiPageWikiLink Q3043143.
- Q5044061 wikiPageWikiLink Q3358135.
- Q5044061 wikiPageWikiLink Q39572.
- Q5044061 wikiPageWikiLink Q6279182.
- Q5044061 wikiPageWikiLink Q6531938.
- Q5044061 wikiPageWikiLink Q6853484.
- Q5044061 wikiPageWikiLink Q6902466.
- Q5044061 wikiPageWikiLink Q7187.
- Q5044061 wikiPageWikiLink Q8444063.
- Q5044061 wikiPageWikiLink Q847583.
- Q5044061 name "Carnitine-acylcarnitine translocase deficiency".
- Q5044061 omim "212138".
- Q5044061 type Disease.
- Q5044061 type Thing.
- Q5044061 type Q12136.
- Q5044061 comment "Carnitine-acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long-chain fatty acids into energy, particularly during periods without food. Carnitine, a natural substance acquired mostly through the diet, is used by cells to process fats and produce energy. People with this disorder have a faulty enzyme that prevents long-chain fatty acids from being transported into the innermost part of the mitochondria for processing.".
- Q5044061 label "Carnitine-acylcarnitine translocase deficiency".
- Q5044061 depiction Autorecessive.svg.
- Q5044061 name "Carnitine-acylcarnitine translocase deficiency".