TH-deficient progressive infantile encephalopathy
MONDO:0100066A tyrosine hydroxylase deficiency in which individuals are extremely sensitive to levodopa therapy. In this very severe form, treatment with levodopa is often limited by intolerable dyskinesias.
Also known as: tyrosine hydroxylase-deficient progressive infantile encephalopathy
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Disease
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Metabolic disease
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Hereditary disease
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Inborn errors of metabolism
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Human disease
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Disease of genetic or genomic mechanism
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Tyrosine hydroxylase deficiency
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Disease by developmental or physiological process
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Disease by etiologic mechanism
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Inborn disorder of biogenic amine metabolism and transport
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