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- Q5514398 subject Q6853484.
- Q5514398 subject Q8824943.
- Q5514398 abstract "GRACILE syndrome is a very rare autosomal recessive genetic disorder, one of the Finnish heritage diseases. It is caused by mutation in BCS1L gene that occurs in 1 out of 1,500,000 live births.GRACILE is an acronym for growth retardation, amino aciduria (amino acids in the urine), cholestasis, iron overload, lactic acidosis, and early death. Other names for this syndrome include Finnish lethal neonatal metabolic syndrome (FLNMS); lactic acidosis, Finnish, with hepatic hemosiderosis; and Fellman syndrome.".
- Q5514398 wikiPageWikiLink Q101244.
- Q5514398 wikiPageWikiLink Q1075923.
- Q5514398 wikiPageWikiLink Q10860654.
- Q5514398 wikiPageWikiLink Q1500373.
- Q5514398 wikiPageWikiLink Q17847759.
- Q5514398 wikiPageWikiLink Q2567857.
- Q5514398 wikiPageWikiLink Q5253500.
- Q5514398 wikiPageWikiLink Q6853484.
- Q5514398 wikiPageWikiLink Q8824943.
- Q5514398 type Disease.
- Q5514398 type Thing.
- Q5514398 type Q12136.
- Q5514398 comment "GRACILE syndrome is a very rare autosomal recessive genetic disorder, one of the Finnish heritage diseases. It is caused by mutation in BCS1L gene that occurs in 1 out of 1,500,000 live births.GRACILE is an acronym for growth retardation, amino aciduria (amino acids in the urine), cholestasis, iron overload, lactic acidosis, and early death.".
- Q5514398 label "GRACILE syndrome".