hawkinsinuria

H4A1W4K5I1N1S1I1N1U1R1I1A1

noun

4-alpha-hydroxyphenylpyruvate hydroxylase deficiency, an autosomal dominant metabolic disorder affecting the metabolism of tyrosine.

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Meanings

nounhawkinsinuria (uncountable)
  1. uncountable4-alpha-hydroxyphenylpyruvate hydroxylase deficiency, an autosomal dominant metabolic disorder affecting the metabolism of tyrosine.

Origin

From hawkinsin + -uria.

Full word history & related roots →
Cite this entry
APA

hawkinsinuria. (n.d.). In WatkinsX Dictionary. Retrieved November 5, 2026, from https://dictionary.watkinsx.com/word/hawkinsinuria

MLA

“hawkinsinuria.” WatkinsX Dictionary, https://dictionary.watkinsx.com/word/hawkinsinuria. Accessed November 5, 2026.

Chicago

WatkinsX Dictionary, s.v. “hawkinsinuria,” accessed November 5, 2026, https://dictionary.watkinsx.com/word/hawkinsinuria.

Source: hawkinsinuria on Wiktionary, CC BY-SA 4.0.