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- Ornithine_translocase_deficiency abstract "Ornithine translocase deficiency, also called hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, is a rare autosomal recessive urea cycle disorder affecting the enzyme ornithine translocase, which causes ammonia to accumulate in the blood, a condition called hyperammonemia. Ammonia, which is formed when proteins are broken down in the body, is toxic if the levels become too high. The nervous system is especially sensitive to the effects of excess ammonia.".
- Ornithine_translocase_deficiency thumbnail L-Ornithine_structure.svg?width=300.
- Ornithine_translocase_deficiency wikiPageExternalLink www.ommbid.com.
- Ornithine_translocase_deficiency wikiPageID "8444293".
- Ornithine_translocase_deficiency wikiPageLength "3952".
- Ornithine_translocase_deficiency wikiPageOutDegree "25".
- Ornithine_translocase_deficiency wikiPageRevisionID "704533290".
- Ornithine_translocase_deficiency wikiPageWikiLink Ammonia.
- Ornithine_translocase_deficiency wikiPageWikiLink Autosome.
- Ornithine_translocase_deficiency wikiPageWikiLink Category:Amino_acid_metabolism_disorders.
- Ornithine_translocase_deficiency wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Ornithine_translocase_deficiency wikiPageWikiLink Category:Rare_diseases.
- Ornithine_translocase_deficiency wikiPageWikiLink Dominance_(genetics).
- Ornithine_translocase_deficiency wikiPageWikiLink Enzyme.
- Ornithine_translocase_deficiency wikiPageWikiLink File:Autorecessive.svg.
- Ornithine_translocase_deficiency wikiPageWikiLink Hyperammonemia.
- Ornithine_translocase_deficiency wikiPageWikiLink Inborn_error_of_metabolism.
- Ornithine_translocase_deficiency wikiPageWikiLink Kidney.
- Ornithine_translocase_deficiency wikiPageWikiLink Liver.
- Ornithine_translocase_deficiency wikiPageWikiLink Metabolic_disorder.
- Ornithine_translocase_deficiency wikiPageWikiLink Mitochondrion.
- Ornithine_translocase_deficiency wikiPageWikiLink Nervous_system.
- Ornithine_translocase_deficiency wikiPageWikiLink Ornithine.
- Ornithine_translocase_deficiency wikiPageWikiLink Ornithine_aminotransferase_deficiency.
- Ornithine_translocase_deficiency wikiPageWikiLink Ornithine_transcarbamylase_deficiency.
- Ornithine_translocase_deficiency wikiPageWikiLink Ornithine_translocase.
- Ornithine_translocase_deficiency wikiPageWikiLink Urea_cycle_disorder.
- Ornithine_translocase_deficiency wikiPageWikiLinkText "Ornithine translocase deficiency".
- Ornithine_translocase_deficiency wikiPageWikiLinkText "hyperornithinemia".
- Ornithine_translocase_deficiency wikiPageWikiLinkText "ornithine translocase deficiency".
- Ornithine_translocase_deficiency caption Ornithine.
- Ornithine_translocase_deficiency diseasesdb "29849".
- Ornithine_translocase_deficiency icd "270.6".
- Ornithine_translocase_deficiency name "Ornithine translocase deficiency".
- Ornithine_translocase_deficiency omim "238970".
- Ornithine_translocase_deficiency wikiPageUsesTemplate Template:Amino_acid_metabolic_pathology.
- Ornithine_translocase_deficiency wikiPageUsesTemplate Template:Infobox_Disease.
- Ornithine_translocase_deficiency wikiPageUsesTemplate Template:NLM.
- Ornithine_translocase_deficiency wikiPageUsesTemplate Template:Refimprove.
- Ornithine_translocase_deficiency wikiPageUsesTemplate Template:Reflist.
- Ornithine_translocase_deficiency subject Category:Amino_acid_metabolism_disorders.
- Ornithine_translocase_deficiency subject Category:Autosomal_recessive_disorders.
- Ornithine_translocase_deficiency subject Category:Rare_diseases.
- Ornithine_translocase_deficiency hypernym Disorder.
- Ornithine_translocase_deficiency type Disease.
- Ornithine_translocase_deficiency type Disorder.
- Ornithine_translocase_deficiency type Error.
- Ornithine_translocase_deficiency comment "Ornithine translocase deficiency, also called hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome, is a rare autosomal recessive urea cycle disorder affecting the enzyme ornithine translocase, which causes ammonia to accumulate in the blood, a condition called hyperammonemia. Ammonia, which is formed when proteins are broken down in the body, is toxic if the levels become too high. The nervous system is especially sensitive to the effects of excess ammonia.".
- Ornithine_translocase_deficiency label "Ornithine translocase deficiency".
- Ornithine_translocase_deficiency sameAs Q7103627.
- Ornithine_translocase_deficiency sameAs سندرم_HHH.
- Ornithine_translocase_deficiency sameAs m.0273nc3.
- Ornithine_translocase_deficiency sameAs Q7103627.
- Ornithine_translocase_deficiency sameAs 高鳥胺酸血症-高氨血症-高瓜胺酸血症候群.
- Ornithine_translocase_deficiency wasDerivedFrom Ornithine_translocase_deficiency?oldid=704533290.
- Ornithine_translocase_deficiency depiction L-Ornithine_structure.svg.
- Ornithine_translocase_deficiency isPrimaryTopicOf Ornithine_translocase_deficiency.