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bn:01031962n
Noun Concept
Categories: Autosomal recessive disorders, Endocrine, nutritional and metabolic disease stubs, Amino acid metabolism disorders
EN
Tyrosinemia type III  Hereditary tyrosinemia, Type III  High tyrosinemia  Hypertyrosinemia type III  Type III tyrosinemia
EN
Tyrosinemia type III is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase, encoded by the gene HPD. Wikipedia
Definitions
Relations
Sources
EN
Tyrosinemia type III is a rare disorder caused by a deficiency of the enzyme 4-hydroxyphenylpyruvate dioxygenase, encoded by the gene HPD. Wikipedia
Tyrosinemia that has material basis in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine Wikidata
IS A
rare disease
tyrosinemia
DRUG USED FOR TREATMENT
sodium ascorbate
nitisinone
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
Tyrosinemia type III
Wikidata
EN
tyrosinemia type III
Wikipedia Redirections
EN
Type III tyrosinemia, tyrosinemia III
Wikidata Alias
EN
Hereditary tyrosinemia, Type III, High tyrosinemia, Hypertyrosinemia type III

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