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- Alpers'_disease abstract "Alpers' disease, also called Alpers' syndrome, progressive sclerosing poliodystrophy, and progressive infantile poliodystrophy, is a progressive degenerative disease of the central nervous system that occurs mostly in infants and children. It is an autosomal recessive disorder meaning two copies of the defective gene is required for active disease, a single copy conveys carrier status. Alpers' disease is caused by certain genetic mutations in the POLG gene.".
- Alpers'_disease diseasesdb "29298".
- Alpers'_disease icd10 "G31.8".
- Alpers'_disease icd9 "330.8".
- Alpers'_disease meshId "D002549".
- Alpers'_disease omim "203700".
- Alpers'_disease wikiPageExternalLink www.haileyswish.org.
- Alpers'_disease wikiPageExternalLink alpersdisease.htm.
- Alpers'_disease wikiPageExternalLink www.thenicholasappeal.co.uk.
- Alpers'_disease wikiPageID "87852".
- Alpers'_disease wikiPageRevisionID "584546139".
- Alpers'_disease diseasesdb "29298".
- Alpers'_disease hasPhotoCollection Alpers'_disease.
- Alpers'_disease icd "330.8".
- Alpers'_disease icd "G31.8".
- Alpers'_disease meshid "D002549".
- Alpers'_disease name "Alpers' disease".
- Alpers'_disease omim "203700".
- Alpers'_disease wordnet_type synset-disease-noun-1.
- Alpers'_disease subject Category:Demyelinating_diseases_of_CNS.
- Alpers'_disease type Abstraction100002137.
- Alpers'_disease type Attribute100024264.
- Alpers'_disease type Condition113920835.
- Alpers'_disease type Disease114070360.
- Alpers'_disease type IllHealth114052046.
- Alpers'_disease type Illness114061805.
- Alpers'_disease type PathologicalState114051917.
- Alpers'_disease type PhysicalCondition114034177.
- Alpers'_disease type State100024720.
- Alpers'_disease type Disease.
- Alpers'_disease type AilmentCondition.
- Alpers'_disease type Situation.
- Alpers'_disease comment "Alpers' disease, also called Alpers' syndrome, progressive sclerosing poliodystrophy, and progressive infantile poliodystrophy, is a progressive degenerative disease of the central nervous system that occurs mostly in infants and children. It is an autosomal recessive disorder meaning two copies of the defective gene is required for active disease, a single copy conveys carrier status. Alpers' disease is caused by certain genetic mutations in the POLG gene.".
- Alpers'_disease label "Alpers' disease".
- Alpers'_disease label "Alpers-Huttenlocher-Syndrom".
- Alpers'_disease label "Choroba Alpersa".
- Alpers'_disease label "Síndrome de Alpers".
- Alpers'_disease label "Ziekte van Alper".
- Alpers'_disease label "Синдром Альперса".
- Alpers'_disease sameAs Alpers-Huttenlocher-Syndrom.
- Alpers'_disease sameAs Ziekte_van_Alper.
- Alpers'_disease sameAs Choroba_Alpersa.
- Alpers'_disease sameAs Síndrome_de_Alpers.
- Alpers'_disease sameAs m.0m1r9.
- Alpers'_disease sameAs Q2028015.
- Alpers'_disease sameAs Q2028015.
- Alpers'_disease sameAs 64.
- Alpers'_disease sameAs Alpers'_disease.
- Alpers'_disease wasDerivedFrom Alpers'_disease?oldid=584546139.
- Alpers'_disease isPrimaryTopicOf Alpers'_disease.
- Alpers'_disease name "Alpers' disease".