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bn:01031962n
Noun Concept
FR
tyrosinémie type 3
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
maladie rare
tyrosinémie
DRUG USED FOR TREATMENT
ascorbate de sodium
nitisinone
HEALTH SPECIALTY
endocrinologie
Wikidata
FR
tyrosinémie type 3

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