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- Q1122668 subject Q6902466.
- Q1122668 subject Q7215445.
- Q1122668 abstract "Tyrosinemia (or "Tyrosinaemia") is an error of metabolism, usually inborn, in which the body cannot effectively break down the amino acid tyrosine. Symptoms include liver and kidney disturbances and mental retardation. Untreated, tyrosinemia can be fatal.Most inborn forms of tyrosinemia produce hypertyrosinemia (high levels of tyrosine).".
- Q1122668 icd10 "E70.2".
- Q1122668 icd9 "270.2".
- Q1122668 meshId "D020176".
- Q1122668 omim "276700".
- Q1122668 thumbnail L-tyrosine-skeletal.png?width=300.
- Q1122668 wikiPageExternalLink abouttyr.htm.
- Q1122668 wikiPageExternalLink br.fcgi?book=gene&part=tyrosinemia.
- Q1122668 wikiPageWikiLink Q1057.
- Q1122668 wikiPageWikiLink Q1507609.
- Q1122668 wikiPageWikiLink Q17067874.
- Q1122668 wikiPageWikiLink Q1747726.
- Q1122668 wikiPageWikiLink Q1758393.
- Q1122668 wikiPageWikiLink Q188017.
- Q1122668 wikiPageWikiLink Q651680.
- Q1122668 wikiPageWikiLink Q6902466.
- Q1122668 wikiPageWikiLink Q6955445.
- Q1122668 wikiPageWikiLink Q7215445.
- Q1122668 wikiPageWikiLink Q7484623.
- Q1122668 wikiPageWikiLink Q7861692.
- Q1122668 wikiPageWikiLink Q8066.
- Q1122668 icd "270.2".
- Q1122668 icd "E70.2".
- Q1122668 meshid "D020176".
- Q1122668 name "Tyrosinemia".
- Q1122668 omim "276700".
- Q1122668 type Disease.
- Q1122668 type Thing.
- Q1122668 type Q12136.
- Q1122668 comment "Tyrosinemia (or "Tyrosinaemia") is an error of metabolism, usually inborn, in which the body cannot effectively break down the amino acid tyrosine. Symptoms include liver and kidney disturbances and mental retardation. Untreated, tyrosinemia can be fatal.Most inborn forms of tyrosinemia produce hypertyrosinemia (high levels of tyrosine).".
- Q1122668 label "Tyrosinemia".
- Q1122668 depiction L-tyrosine-skeletal.png.
- Q1122668 name "Tyrosinemia".