Basal Ganglia Calcification

Alias:
Fahr's Syndrome
Fahr's Disease
Fahr Disease
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Basal Ganglia Calcification, also known as fahr's syndrome, is related to basal ganglia calcification, idiopathic, 1 and aicardi-goutieres syndrome, and has symptoms including athetosis, cerebellar ataxia and muscle rigidity. An important gene associated with Basal Ganglia Calcification is SLC20A2 (Solute Carrier Family 20 Member 2), and among its related pathways/superpathways are Overview of interferons-mediated signaling pathway and Nectin adhesion pathway. The drug Etidronic acid has been mentioned in the context of this disorder. Affiliated tissues include cortex and brain, and related phenotypes are immune system and embryo
Related ID:
MESH:C536275

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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37
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10

Medical Symptom

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Description
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No data available

Gene & Mutation

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Related Drugs

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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