Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Infantile_neuronal_ceroid_lipofuscinosis> ?p ?o }
Showing triples 1 to 54 of
54
with 100 triples per page.
- Infantile_neuronal_ceroid_lipofuscinosis 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.".
- Infantile_neuronal_ceroid_lipofuscinosis meshId "D009472".
- Infantile_neuronal_ceroid_lipofuscinosis omim "256730".
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageExternalLink NBK1428.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageExternalLink www.incl.fi.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageExternalLink incl-ja-ncl-taudit.html.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageID "2217803".
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageLength "3248".
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageOutDegree "18".
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageRevisionID "683184241".
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Autosome.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Category:Lipid_storage_disorders.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Cysteamine.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Dominance_(genetics).
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Epilepsy.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink FAIDD.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Finland.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Founder_effect.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Genetics.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Hearing.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Myoclonus.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Neuronal_ceroid_lipofuscinosis.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Palmitoyl_protein_thioesterase.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Physical_therapy.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Somatosensory_system.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Speech.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLink Visual_impairment.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLinkText "Infantile neuronal ceroid lipofuscinosis".
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageWikiLinkText "infantile neuronal ceroid lipofuscinosis".
- Infantile_neuronal_ceroid_lipofuscinosis diseasesdb "31533".
- Infantile_neuronal_ceroid_lipofuscinosis meshid "D009472".
- Infantile_neuronal_ceroid_lipofuscinosis name "Infantile neuronal ceroid lipfuscinosis".
- Infantile_neuronal_ceroid_lipofuscinosis omim "256730".
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageUsesTemplate Template:Citation_needed.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageUsesTemplate Template:Infobox_disease.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageUsesTemplate Template:Lipid_storage_disorders.
- Infantile_neuronal_ceroid_lipofuscinosis wikiPageUsesTemplate Template:Reflist.
- Infantile_neuronal_ceroid_lipofuscinosis subject Category:Lipid_storage_disorders.
- Infantile_neuronal_ceroid_lipofuscinosis hypernym Form.
- Infantile_neuronal_ceroid_lipofuscinosis type Disease.
- Infantile_neuronal_ceroid_lipofuscinosis type Disorder.
- Infantile_neuronal_ceroid_lipofuscinosis type Thing.
- Infantile_neuronal_ceroid_lipofuscinosis type Q12136.
- Infantile_neuronal_ceroid_lipofuscinosis 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.".
- Infantile_neuronal_ceroid_lipofuscinosis label "Infantile neuronal ceroid lipofuscinosis".
- Infantile_neuronal_ceroid_lipofuscinosis sameAs Q4357262.
- Infantile_neuronal_ceroid_lipofuscinosis sameAs INCL-tauti.
- Infantile_neuronal_ceroid_lipofuscinosis sameAs Choroba_Santavuoriego-Haltii.
- Infantile_neuronal_ceroid_lipofuscinosis sameAs m.06wrk3.
- Infantile_neuronal_ceroid_lipofuscinosis sameAs Болезнь_Сантавуори_—_Халтиа.
- Infantile_neuronal_ceroid_lipofuscinosis sameAs Q4357262.
- Infantile_neuronal_ceroid_lipofuscinosis wasDerivedFrom Infantile_neuronal_ceroid_lipofuscinosis?oldid=683184241.
- Infantile_neuronal_ceroid_lipofuscinosis isPrimaryTopicOf Infantile_neuronal_ceroid_lipofuscinosis.
- Infantile_neuronal_ceroid_lipofuscinosis name "Infantile neuronal ceroid lipfuscinosis".