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Fahr's syndrome
Idiopathic Basal Ganglia Calcification, also known as Fahr disease or Fahr’s Syndrome is a rare, genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement, including the basal ganglia and the cerebral cortex.
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Primrose syndrome
Genetic disorders with OMIM but no gene
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Neurological disorders
Rare diseases
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