Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Leukoencephalopathy_with_vanishing_white_matter> ?p ?o }
- Leukoencephalopathy_with_vanishing_white_matter genereviewsname "CARASIL Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, Maeda Syndrome".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsname "Childhood Ataxia with Central Nervous System Hypomylenation/Vanishing White Matter".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsnbk "NBK1258".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsnbk "NBK1500".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsnbk "NBK32533".
- Leukoencephalopathy_with_vanishing_white_matter hasPhotoCollection Leukoencephalopathy_with_vanishing_white_matter.
- Leukoencephalopathy_with_vanishing_white_matter name "Leukoencephalopathy with vanishing white matter".
- Leukoencephalopathy_with_vanishing_white_matter omim "603896".
- Leukoencephalopathy_with_vanishing_white_matter omimMult "CARASIL: CADASIL:".
- Leukoencephalopathy_with_vanishing_white_matter wikiPageUsesTemplate Template:CNS_diseases_of_the_nervous_system.
- Leukoencephalopathy_with_vanishing_white_matter wikiPageUsesTemplate Template:Cite_journal.
- Leukoencephalopathy_with_vanishing_white_matter wikiPageUsesTemplate Template:Disorders_of_translation_and_posttranslational_modification.
- Leukoencephalopathy_with_vanishing_white_matter wikiPageUsesTemplate Template:Infobox_Disease.
- Leukoencephalopathy_with_vanishing_white_matter wikiPageUsesTemplate Template:Reflist.
- Leukoencephalopathy_with_vanishing_white_matter subject Category:Demyelinating_diseases_of_CNS.
- Leukoencephalopathy_with_vanishing_white_matter subject Category:Mental_disorders_due_to_a_general_medical_condition.
- Leukoencephalopathy_with_vanishing_white_matter subject Category:Rare_diseases.
- Leukoencephalopathy_with_vanishing_white_matter hypernym Disease.
- Leukoencephalopathy_with_vanishing_white_matter type Disease.
- Leukoencephalopathy_with_vanishing_white_matter type Disorder.
- Leukoencephalopathy_with_vanishing_white_matter comment "Leukoencephalopathy with vanishing white matter (VWM disease) is an autosomal recessive neurological disease. The cause of the disease are mutations in any of the 5 genes encoding subunits of the translation initiation factor EIF-2B: EIF2B1, EIF2B2, EIF2B3, EIF2B4, or EIF2B5. The disease belongs to a family of conditions called the Leukodystrophies.".
- Leukoencephalopathy_with_vanishing_white_matter label "Leukoencephalopathy with vanishing white matter".
- Leukoencephalopathy_with_vanishing_white_matter sameAs Leucoencefalopatía_con_desaparición_da_substancia_branca.
- Leukoencephalopathy_with_vanishing_white_matter sameAs Leukoencefalopatia_z_zanikającą_istotą_białą.
- Leukoencephalopathy_with_vanishing_white_matter sameAs m.02rw1ck.
- Leukoencephalopathy_with_vanishing_white_matter sameAs Q6534523.
- Leukoencephalopathy_with_vanishing_white_matter sameAs Q6534523.
- Leukoencephalopathy_with_vanishing_white_matter wasDerivedFrom Leukoencephalopathy_with_vanishing_white_matter?oldid=679825144.
- Leukoencephalopathy_with_vanishing_white_matter isPrimaryTopicOf Leukoencephalopathy_with_vanishing_white_matter.