2026 ICD-10-CM Diagnosis Code P74.5Transitory tyrosinemia of newborn
ICD-10-CM Codes›P00–P96›P70-P74›P74
- Billable — Valid for Submission
- Not Chronic
P74.5 is a billable ICD-10-CM diagnosis code for transitory tyrosinemia of newborn. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026). Coders also document this condition as hypertyrosinemia. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other specified and unspecified perinatal conditions.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Hypertyrosinemia
- Neonatal metabolic acidemia
- Transient neonatal hypertyrosinemia
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Tyrosinemia - E70.21
- newborn, transitory - P74.5
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Tyrosinemia
- newborn, transitory
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Tyrosinemia
an autosomal recessive inherited metabolic disorder caused by mutations in the fah, hpd, and tat genes. it is characterized by deficiency of one of the enzymes that are involved in the metabolism of tyrosine. it results in elevated blood tyrosine levels and accumulation of tyrosine and its byproducts in the liver, kidney, nervous system and other organs.Tyrosinemia Type I|Type I Tyrosinemia
tyrosinemia caused by mutations in the fah gene. it is characterized by deficiency of the enzyme fumarylacetoacetate hydrolase. it is the most severe form of tyrosinemia. signs and symptoms appear early in life and include failure to thrive, vomiting, diarrhea, jaundice, and bleeding tendency. it may result in liver and kidney failure. patients with this type of tyrosinemia may also have a predisposition for hepatocellular carcinoma.Tyrosinemia Type II
tyrosinemia caused by mutation(s) in the tat gene, encoding tyrosine aminotransferase. the inheritance is autosomal recessive.
Patient EducationClinical
Metabolic Disorders
Metabolism is the process your body uses to get or make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive system break the food parts down into sugars and acids, your body's fuel.
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Convert P74.5 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About P74.5Overview
Is P74.5 a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report transitory tyrosinemia of newborn on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What is the ICD-9 equivalent of P74.5?
Under the General Equivalence Mappings, transitory tyrosinemia of newborn converts to ICD-9-CM 775.89 (neonat endo/met dis NEC). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Not chronic - A diagnosis code that does not fit the criteria for chronic condition (duration, ongoing medical treatment, and limitations) is considered not chronic. Some codes designated as not chronic are acute conditions. Other diagnosis codes that indicate a possible chronic condition, but for which the duration of the illness is not specified in the code description (i.e., we do not know the condition has lasted 12 months or longer) also are considered not chronic.
