tyrosinemia

American  

[tahy-roh-si-nee-mee-uh, tir-oh-] / ˌtaɪ roʊ sɪˈni mi ə, ˌtɪr oʊ- /

noun

Pathology.

1. an inherited disorder of tyrosine metabolism that can lead to liver and kidney disease and intellectual disability unless controlled by a special diet.

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Etymology

Origin of tyrosinemia

First recorded in 1960–65; tyrosine + -emia

Example Sentences

In people, the inherited liver disease that the scientists targeted in mice, called hereditary tyrosinemia type 1, starts damaging the liver months before birth.

From Scientific American

Mice that have been genetically modified to develop hereditary tyrosinemia, a human liver disease, will resist the disease if they also lose another gene on chromosome 16 called homogentisic acid dioxygenase.

From Scientific American

The Philadelphia scientists then tried their technique on hereditary tyrosinemia type 1.

From Scientific American