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- VLDLR-associated_cerebellar_hypoplasia abstract "VLDLR-associated cerebellar hypoplasia (VLDLRCH; alternative names: dysequilibrium syndrome, DES; nonprogressive cerebellar disorder with mental retardation) is a rare autosomal recessive condition caused by a disruption of the VLDLR gene. First described as a form of cerebral palsy in the 1970s, it is associated with parental consanguinity and is found in secluded communities, with a number of cases described in Hutterite families.".
- VLDLR-associated_cerebellar_hypoplasia omim "224050".
- VLDLR-associated_cerebellar_hypoplasia wikiPageExternalLink br.fcgi?book=gene&part=vldlr-ch.
- VLDLR-associated_cerebellar_hypoplasia wikiPageExternalLink dispomim.cgi?id=224050.
- VLDLR-associated_cerebellar_hypoplasia wikiPageID "14553603".
- VLDLR-associated_cerebellar_hypoplasia wikiPageRevisionID "545050849".
- VLDLR-associated_cerebellar_hypoplasia hasPhotoCollection VLDLR-associated_cerebellar_hypoplasia.
- VLDLR-associated_cerebellar_hypoplasia omim "224050".
- VLDLR-associated_cerebellar_hypoplasia subject Category:Congenital_disorders_of_nervous_system.
- VLDLR-associated_cerebellar_hypoplasia type Abnormality114501726.
- VLDLR-associated_cerebellar_hypoplasia type Abstraction100002137.
- VLDLR-associated_cerebellar_hypoplasia type Anomaly114505821.
- VLDLR-associated_cerebellar_hypoplasia type Attribute100024264.
- VLDLR-associated_cerebellar_hypoplasia type BirthDefect114465048.
- VLDLR-associated_cerebellar_hypoplasia type Condition113920835.
- VLDLR-associated_cerebellar_hypoplasia type CongenitalDisordersOfNervousSystem.
- VLDLR-associated_cerebellar_hypoplasia type Defect114464005.
- VLDLR-associated_cerebellar_hypoplasia type Disease114070360.
- VLDLR-associated_cerebellar_hypoplasia type IllHealth114052046.
- VLDLR-associated_cerebellar_hypoplasia type Illness114061805.
- VLDLR-associated_cerebellar_hypoplasia type Imperfection114462666.
- VLDLR-associated_cerebellar_hypoplasia type PathologicalState114051917.
- VLDLR-associated_cerebellar_hypoplasia type PhysicalCondition114034177.
- VLDLR-associated_cerebellar_hypoplasia type State100024720.
- VLDLR-associated_cerebellar_hypoplasia type Disease.
- VLDLR-associated_cerebellar_hypoplasia type AilmentCondition.
- VLDLR-associated_cerebellar_hypoplasia type Situation.
- VLDLR-associated_cerebellar_hypoplasia comment "VLDLR-associated cerebellar hypoplasia (VLDLRCH; alternative names: dysequilibrium syndrome, DES; nonprogressive cerebellar disorder with mental retardation) is a rare autosomal recessive condition caused by a disruption of the VLDLR gene. First described as a form of cerebral palsy in the 1970s, it is associated with parental consanguinity and is found in secluded communities, with a number of cases described in Hutterite families.".
- VLDLR-associated_cerebellar_hypoplasia label "VLDLR-associated cerebellar hypoplasia".
- VLDLR-associated_cerebellar_hypoplasia label "VLDLR-ассоциированная мозжечковая гипоплазия".
- VLDLR-associated_cerebellar_hypoplasia sameAs m.03d7q0x.
- VLDLR-associated_cerebellar_hypoplasia sameAs Q4052543.
- VLDLR-associated_cerebellar_hypoplasia sameAs Q4052543.
- VLDLR-associated_cerebellar_hypoplasia sameAs VLDLR-associated_cerebellar_hypoplasia.
- VLDLR-associated_cerebellar_hypoplasia wasDerivedFrom VLDLR-associated_cerebellar_hypoplasia?oldid=545050849.
- VLDLR-associated_cerebellar_hypoplasia isPrimaryTopicOf VLDLR-associated_cerebellar_hypoplasia.