Catalog

Tyrosinaemia type 2

5C50.12

Link to WHO Definition

Tyrosinaemia type 2 – http://id.who.int/icd/entity/1900229795

Tyrosinemia type 2 is an inborn error of tyrosine metabolism characterised by hypertyrosinemia with oculocutaneous manifestations (eye redness, photophobia, excessive tearing and pain, palmoplantar hyperkeratosis) and, in some cases, intellectual deficit.

Parents