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bn:01031962n
Noun Concept
EL
No term available
EN
Tyrosinemia type III is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase, encoded by the gene HPD. Wikipedia
Relations
Sources
IS A
σπάνια πάθηση
τυροσιναιμία
DRUG USED FOR TREATMENT
ασκορβικό νάτριο
EN
nitisinone
HEALTH SPECIALTY
ενδοκρινολογία

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