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bn:03195375n
Noun Concept
Categories: Autosomal dominant disorders, Genetic disorder stubs, Amino acid metabolism disorders
EN
hawkinsinuria  4-alpha-hydroxyphenylpyruvate hydroxylase deficiency  4-HPPD deficiency  4-hydroxyphenylpyruvic acid dioxygenase deficiency  4 alpha hydroxyphenylpyruvate hydroxylase deficiency
EN
Hawkinsinuria is an autosomal dominant metabolic disorder affecting the metabolism of tyrosine. Wikipedia
Definitions
Relations
Sources
EN
Hawkinsinuria is an autosomal dominant metabolic disorder affecting the metabolism of tyrosine. Wikipedia
4-alpha-hydroxyphenylpyruvate hydroxylase deficiency, an autosomal dominant metabolic disorder affecting the metabolism of tyrosine. Wiktionary
IS A
disease
rare disease
tyrosinemia
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
hawkinsinuria
Wikidata
EN
hawkinsinuria
Wiktionary
EN
hawkinsinuria
Wikipedia Redirections
EN
4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency, 4 alpha hydroxyphenylpyruvate hydroxylase deficiency
Wikidata Alias
EN
4-alpha-hydroxyphenylpyruvate hydroxylase deficiency, 4-HPPD deficiency, 4-hydroxyphenylpyruvic acid dioxygenase deficiency, HAWKINSINURIA

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