E80ICD-10-CM 2027
Disorders of porphyrin and bilirubin metabolism
Untergeordnete Codes
E80.0– Hereditary erythropoietic porphyriaE80.1– Porphyria cutanea tardaE80.2– Other and unspecified porphyriaE80.3– Defects of catalase and peroxidaseE80.4– Gilbert syndromeE80.5– Crigler-Najjar syndromeE80.6– Other disorders of bilirubin metabolismE80.7– Disorder of bilirubin metabolism, unspecified
Includes
- defects of catalase and peroxidase