Tyrosinemia Type I is a rare genetic disorder that affects the breakdown of the amino acid tyrosine. The ICD10 code for Tyrosinemia Type I is E70.2. In the previous coding system, the ICD9 code for this condition was 270.2. It is important to consult with a healthcare professional for accurate diagnosis and appropriate treatment of this condition.
Tyrosinemia Type I, also known as hepatorenal tyrosinemia or tyrosinemia with acute hepatic crisis, is a rare genetic disorder that affects the body's ability to break down the amino acid tyrosine. The ICD-10 code for Tyrosinemia Type I is E70.2. This code falls under the category of "Disorders of aromatic amino-acid metabolism" in the ICD-10 coding system.
In the previous ICD-9 coding system, Tyrosinemia Type I was classified under code 270.2. The ICD-9 code system was used until September 30, 2015, when it was replaced by the ICD-10 system. The transition to ICD-10 allowed for more detailed and specific coding, thus offering improved accuracy in diagnosing and tracking medical conditions.
It is important to note that ICD codes are used for billing and statistical purposes, helping healthcare providers and researchers classify and analyze diseases. However, they do not provide detailed information about the condition itself or its treatment. For specific medical advice or information, it is always recommended to consult with a qualified healthcare professional.