tyrosinemia type II (Q7484623)

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A tyrosinemia that has_material_basis_in deficiency of hepatic tyrosine aminotransferase located_in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels.
  • tyrosinemia type II
  • Oculocutaneous tyrosinemia
  • Richner-Hanhart syndrome
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English
tyrosinemia type II
A tyrosinemia that has_material_basis_in deficiency of hepatic tyrosine aminotransferase located_in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels.
  • tyrosinemia type II
  • Oculocutaneous tyrosinemia
  • Richner-Hanhart syndrome

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