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ornithine aminotransferase deficiency

Wikipedia Summary

Ornithine aminotransferase deficiency (also known as gyrate atrophy of the choroid and retina) is an inborn error of ornithine metabolism, caused by decreased activity of the enzyme ornithine aminotransferase. Biochemically, it can be detected by elevated levels of ornithine in the blood...
Related Codes (1)
Code
Description
Billable
Details
H31.23Gyrate atrophy, choroid

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