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- Q4357262 subject Q6902390.
- Q4357262 abstract "Infantile neuronal ceroid lipofuscinoses (INCL) or Santavuori disease is a form of NCL and inherited as a recessive autosomal genetic trait. The disorder is progressive, degenerative and fatal, extremely rare worldwide – with approximately 60 official cases reported by 1982, perhaps 100 sufferers in total today – but relatively common in Finland due to the local founder effect.".
- Q4357262 meshId "D009472".
- Q4357262 omim "256730".
- Q4357262 wikiPageExternalLink NBK1428.
- Q4357262 wikiPageExternalLink www.incl.fi.
- Q4357262 wikiPageExternalLink incl-ja-ncl-taudit.html.
- Q4357262 wikiPageWikiLink Q116275.
- Q4357262 wikiPageWikiLink Q160289.
- Q4357262 wikiPageWikiLink Q186005.
- Q4357262 wikiPageWikiLink Q186380.
- Q4357262 wikiPageWikiLink Q328835.
- Q4357262 wikiPageWikiLink Q33.
- Q4357262 wikiPageWikiLink Q41571.
- Q4357262 wikiPageWikiLink Q4358039.
- Q4357262 wikiPageWikiLink Q504568.
- Q4357262 wikiPageWikiLink Q52946.
- Q4357262 wikiPageWikiLink Q5424329.
- Q4357262 wikiPageWikiLink Q617563.
- Q4357262 wikiPageWikiLink Q6531938.
- Q4357262 wikiPageWikiLink Q6902390.
- Q4357262 wikiPageWikiLink Q7128407.
- Q4357262 wikiPageWikiLink Q7162.
- Q4357262 wikiPageWikiLink Q737460.
- Q4357262 meshid "D009472".
- Q4357262 name "Infantile neuronal ceroid lipfuscinosis".
- Q4357262 omim "256730".
- Q4357262 type Disease.
- Q4357262 type Thing.
- Q4357262 type Q12136.
- Q4357262 comment "Infantile neuronal ceroid lipofuscinoses (INCL) or Santavuori disease is a form of NCL and inherited as a recessive autosomal genetic trait. The disorder is progressive, degenerative and fatal, extremely rare worldwide – with approximately 60 official cases reported by 1982, perhaps 100 sufferers in total today – but relatively common in Finland due to the local founder effect.".
- Q4357262 label "Infantile neuronal ceroid lipofuscinosis".
- Q4357262 name "Infantile neuronal ceroid lipfuscinosis".