phenylketonuria

/fen-l-kee-toh-noor-ee-uh, -nyoor-, feen-/US // ˌfɛn lˌki toʊˈnʊər i ə, -ˈnyʊər-, ˌfin- //UK // (ˌfiːnaɪlˌkiːtəˈnjʊərɪə) //

苯丙酮尿症,苯酮尿症,苯基酮尿症,苯丙酮酸尿症

Definitions

n.名词 noun

1
Pathology.
- : an inherited disease due to faulty metabolism of phenylalanine, characterized by phenyl ketones in the urine and usually first noted by signs of intellectual disability in infancy.