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- Q2214869 subject Q8413585.
- Q2214869 subject Q8482268.
- Q2214869 abstract "Cerebellar hypoplasia is a heterogeneous group of disorder of cerebellar maldevelopment presenting as early onset non progressive ataxia, hypotonia, and motor learning disability. Various causes has been incriminated like hereditary, metabolic, toxic and viral agents. First reported by Crouzon in 1929. In 1940 an unclaimed body came for dissection in London Hospital and was discovered to have no cerebellum. This unique case was appropriately named "human brain without a cerebellum" and was used every year in the Department of Anatomy at Cambridge University in a neuroscience course for medical students.".
- Q2214869 icd10 "Q04.3".
- Q2214869 icd9 "742.2".
- Q2214869 omim "213000".
- Q2214869 wikiPageExternalLink 213000.
- Q2214869 wikiPageExternalLink www.actcerebellarhypoplasia.org.au.
- Q2214869 wikiPageExternalLink intro.htm.
- Q2214869 wikiPageExternalLink watch?v=Dox3_ox8C2U.
- Q2214869 wikiPageWikiLink Q1057.
- Q2214869 wikiPageWikiLink Q130983.
- Q2214869 wikiPageWikiLink Q1753547.
- Q2214869 wikiPageWikiLink Q178694.
- Q2214869 wikiPageWikiLink Q184651.
- Q2214869 wikiPageWikiLink Q213373.
- Q2214869 wikiPageWikiLink Q35794.
- Q2214869 wikiPageWikiLink Q7374421.
- Q2214869 wikiPageWikiLink Q808.
- Q2214869 wikiPageWikiLink Q8413585.
- Q2214869 wikiPageWikiLink Q8482268.
- Q2214869 icd "742.2".
- Q2214869 icd "Q04.3".
- Q2214869 omim "213000".
- Q2214869 type Disease.
- Q2214869 type Thing.
- Q2214869 type Q12136.
- Q2214869 comment "Cerebellar hypoplasia is a heterogeneous group of disorder of cerebellar maldevelopment presenting as early onset non progressive ataxia, hypotonia, and motor learning disability. Various causes has been incriminated like hereditary, metabolic, toxic and viral agents. First reported by Crouzon in 1929. In 1940 an unclaimed body came for dissection in London Hospital and was discovered to have no cerebellum.".
- Q2214869 label "Cerebellar hypoplasia".