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bn:00078840n
Noun Concept
Categories: Amino acid metabolism disorders, Autosomal recessive disorders
EN
tyrosinemia  Disorder of tyrosine metabolism  Hereditary Tyrosinemias  Hypertyrosinemia  tyrosinaemia
EN
Autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation WordNet 3.0
Definitions
Relations
Sources
EN
Autosomal recessive defect in tyrosine metabolism resulting in liver and kidney disturbances and mental retardation WordNet 3.0 & Open English WordNet
Tyrosinemia or tyrosinaemia is an error of metabolism, usually inborn, in which the body cannot effectively break down the amino acid tyrosine. Wikipedia
Amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine Wikidata
A metabolic disorder characterized by the presence of excess tyrosine in the blood. Wiktionary
Metabolic disorder characterized by the presence of excess tyrosine in the blood. Wiktionary (translation)
IS A
autosomal recessive disease
HAS KIND
alkaptonuria
Tyrosinemia type I
Tyrosinemia type III
Tyrosinemia type II
hawkinsinuria
HEALTH SPECIALTY
medical genetics
WordNet 3.0 & Open English WordNet
EN
tyrosinemia
Wikipedia
EN
tyrosinemia
Wikidata
EN
tyrosinemia
Wiktionary
EN
tyrosinemia
Wikipedia Redirections
EN
Hereditary Tyrosinemias, Hypertyrosinemia, tyrosinaemia, Tyrosinemia I, tyrosinemias
Wikidata Alias
EN
Disorder of tyrosine metabolism

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