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- Fahr's_syndrome abstract "Idiopathic Basal Ganglia Calcification, also known as Fahr disease, is a rare, genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement. Through the use of CT scans, calcifications are seen primarily in the basal ganglia and in other areas such as the cerebral cortex.".
- Fahr's_syndrome diseasesdb "32200".
- Fahr's_syndrome icd10 "G23.8".
- Fahr's_syndrome omim "213600".
- Fahr's_syndrome thumbnail Fahr_syndrome.gif?width=300.
- Fahr's_syndrome wikiPageExternalLink top.
- Fahr's_syndrome wikiPageExternalLink kamni-byvaut-ne-tolko-v-pockah-no-i-v-mozge-.
- Fahr's_syndrome wikiPageExternalLink www.nia.nih.gov.
- Fahr's_syndrome wikiPageExternalLink www.nimh.nih.gov.
- Fahr's_syndrome wikiPageExternalLink www.rarediseases.org.
- Fahr's_syndrome wikiPageID "850801".
- Fahr's_syndrome wikiPageRevisionID "605597606".
- Fahr's_syndrome caption "Idiopathic Basal Ganglia Calcification".
- Fahr's_syndrome diseasesdb "32200".
- Fahr's_syndrome genereviewsname "Familial Idiopathic Basal Ganglia Calcification".
- Fahr's_syndrome genereviewsnbk "NBK1421".
- Fahr's_syndrome hasPhotoCollection Fahr's_syndrome.
- Fahr's_syndrome icd "G23.8".
- Fahr's_syndrome name "Fahr's syndrome".
- Fahr's_syndrome omim "213600".
- Fahr's_syndrome wordnet_type synset-disease-noun-1.
- Fahr's_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Fahr's_syndrome subject Category:Neurological_disorders.
- Fahr's_syndrome subject Category:Rare_diseases.
- Fahr's_syndrome subject Category:Syndromes.
- Fahr's_syndrome type Abstraction100002137.
- Fahr's_syndrome type Attribute100024264.
- Fahr's_syndrome type Condition113920835.
- Fahr's_syndrome type Disease114070360.
- Fahr's_syndrome type Disorder114052403.
- Fahr's_syndrome type GeneticDisease114151139.
- Fahr's_syndrome type GeneticDisordersWithOMIMButNoGene.
- Fahr's_syndrome type IllHealth114052046.
- Fahr's_syndrome type Illness114061805.
- Fahr's_syndrome type NervousDisorder114084880.
- Fahr's_syndrome type NeurologicalDisorders.
- Fahr's_syndrome type PathologicalState114051917.
- Fahr's_syndrome type PhysicalCondition114034177.
- Fahr's_syndrome type State100024720.
- Fahr's_syndrome type Disease.
- Fahr's_syndrome type AilmentCondition.
- Fahr's_syndrome type Situation.
- Fahr's_syndrome comment "Idiopathic Basal Ganglia Calcification, also known as Fahr disease, is a rare, genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement. Through the use of CT scans, calcifications are seen primarily in the basal ganglia and in other areas such as the cerebral cortex.".
- Fahr's_syndrome label "Choroba Fahra".
- Fahr's_syndrome label "Fahr's syndrome".
- Fahr's_syndrome label "Morbus Fahr".
- Fahr's_syndrome label "Sindrome di Fahr".
- Fahr's_syndrome label "Syndrome de Fahr".
- Fahr's_syndrome label "Síndrome de Fahr".
- Fahr's_syndrome label "Идиопатическая кальцификация базальных ганглиев 1".
- Fahr's_syndrome label "ファール病".
- Fahr's_syndrome sameAs Morbus_Fahr.
- Fahr's_syndrome sameAs Νόσος_του_Fahr.
- Fahr's_syndrome sameAs Síndrome_de_Fahr.
- Fahr's_syndrome sameAs Syndrome_de_Fahr.
- Fahr's_syndrome sameAs Sindrome_di_Fahr.
- Fahr's_syndrome sameAs ファール病.
- Fahr's_syndrome sameAs Choroba_Fahra.
- Fahr's_syndrome sameAs m.02pxr0t.
- Fahr's_syndrome sameAs Q1947307.
- Fahr's_syndrome sameAs Q1947307.
- Fahr's_syndrome sameAs Fahr's_syndrome.
- Fahr's_syndrome wasDerivedFrom Fahr's_syndrome?oldid=605597606.
- Fahr's_syndrome depiction Fahr_syndrome.gif.
- Fahr's_syndrome isPrimaryTopicOf Fahr's_syndrome.
- Fahr's_syndrome name "Fahr's syndrome".
