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A rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement

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dbo:description
  • Krankheit (de)
  • مرض من الأمراض (ar)
  • хвороба (uk)
  • a rare, genetic neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement (en)
  • maladie se traduisant par des calcifications massives des noyaux gris centraux en l'absence d'anomalie du métabolisme du calcium (fr)
  • calcificazione idiopatica dei nuclei della base (telencefalo), anche nota come Morbo di Fahr, è una rara malattia genetica autosomica dominante (it)
dbo:diseasesDB
  • 32200
dbo:geneReviewsId
  • NBK1421
dbo:geneReviewsName
  • Familial Idiopathic Basal Ganglia Calcification (en)
dbo:icd10
  • G23.8
dbo:omim
  • 213600 (xsd:integer)
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dbo:wikiPageExternalLink
dbo:wikiPageWikiLink
dbp:caption
  • CT scan of characteristic calcifications of the disease (en)
dbp:diseasesdb
  • 32200 (xsd:integer)
dbp:genereviewsname
  • Familial Idiopathic Basal Ganglia Calcification (en)
dbp:genereviewsnbk
  • NBK1421 (en)
dbp:icd
  • (en)
  • G23.8 (en)
dbp:name
  • Primary familial brain calcification (en)
dbp:omim
  • 213600 (xsd:integer)
dbp:synonyms
  • Familial idiopathic basal ganglia calcification (en)
dbp:wikiPageUsesTemplate
dct:subject
rdf:type
rdfs:label
  • Primary familial brain calcification (en)
  • متلازمة فار (ar)
  • Síndrome de Fahr (ca)
  • Νόσος του Φαρ (el)
  • Síndrome de Fahr (es)
  • Morbus Fahr (de)
  • Syndrome de Fahr (fr)
  • Sindrome di Fahr (it)
  • ファール病 (ja)
  • Choroba Fahra (pl)
  • Идиопатическая кальцификация базальных ганглиев 1 (ru)
owl:sameAs
prov:wasDerivedFrom
foaf:depiction
foaf:isPrimaryTopicOf
foaf:name
  • Primary familial brain calcification (en)
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