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5C50.1 Disorders of tyrosine metabolism

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

code elsewhere

• Transitory tyrosinaemia of newborn  (KB63.4)
• Autosomal recessive dopa-responsive dystonia  (8A02.11)
• Oculocutaneous albinism type 1A  (EC23.20)
• Oculocutaneous albinism type 1B  (EC23.20)

sections/codes in this section (5C50.1-5C50.1)

• Alkaptonuria  (5C50.10)
• Tyrosinaemia type 1  (5C50.11)
• Tyrosinaemia type 2  (5C50.12)
• Other specified disorders of tyrosine metabolism  (5C50.1Y)
• Disorders of tyrosine metabolism, unspecified  (5C50.1Z)

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