The ICD-10 code for Tyrosinemia type II is E70.2, while the ICD-9 code is 270.2. Tyrosinemia type II is a rare genetic disorder characterized by a deficiency of the enzyme tyrosine aminotransferase. This condition leads to the accumulation of tyrosine and its byproducts in the body, causing various symptoms such as intellectual disability, liver and kidney problems, and eye abnormalities. Early diagnosis and treatment are crucial for managing this condition.