Tyrosinemia type II

MONDO:0010160

Tyrosinemia type 2 is an inborn error of tyrosine metabolism characterized by hypertyrosinemia with oculocutaneous manifestations and, in some cases, intellectual deficit.

Also known as: Richner-Hanhart syndrome, keratosis palmoplantaris-corneal dystrophy syndrome, oculocutaneous tyrosinemia, tyrosinemia due to TAT deficiency, tyrosinemia due to tyrosine aminotransferase deficiency, tyrosinemia type II, Oregon type tyrosinemia, Richner Hanhart syndrome

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