The ICD-10 code for Hereditary erythropoietic porphyria is E80.0.2026 ICD-10-CM Diagnosis Code E80.0 – Hereditary erythropoietic porphyria Related ICD-10 Codes Parent code: E80 – Disorders of porphyrin and bilirubin metabolism Other codes in same category: E80.1 – Porphyria cutanea tarda, E80.2 – Other and unspecified porphyria, E80.20 – Unspecified porphyria, E80.21 – Acute intermittent (hepatic)…

The ICD-10 code for Disorders of porphyrin and bilirubin metabolism is E80.2026 ICD-10-CM Diagnosis Code E80 – Disorders of porphyrin and bilirubin metabolism Related ICD-10 Codes More specific subcodes: E80.0 – Hereditary erythropoietic porphyria, E80.1 – Porphyria cutanea tarda, E80.2 – Other and unspecified porphyria, E80.20 – Unspecified porphyria, E80.21 – Acute intermittent (hepatic) porphyria,…

The ICD-10 code for Disorder of purine and pyrimidine metabolism, unspecified is E79.9.2026 ICD-10-CM Diagnosis Code E79.9 – Disorder of purine and pyrimidine metabolism, unspecified Related ICD-10 Codes Parent code: E79 – Disorders of purine and pyrimidine metabolism Other codes in same category: E79.0 – Hyperuricemia without signs of inflammatory arthritis and tophaceous disease, E79.1…

The ICD-10 code for Other specified disorders of purine and pyrimidine metabolism is E79.89.2026 ICD-10-CM Diagnosis Code E79.89 – Other specified disorders of purine and pyrimidine metabolism Related ICD-10 Codes Parent code: E79 – Disorders of purine and pyrimidine metabolism Other codes in same category: E79.0 – Hyperuricemia without signs of inflammatory arthritis and tophaceous…

The ICD-10 code for Hereditary xanthinuria is E79.82.2026 ICD-10-CM Diagnosis Code E79.82 – Hereditary xanthinuria Related ICD-10 Codes Parent code: E79 – Disorders of purine and pyrimidine metabolism Other codes in same category: E79.0 – Hyperuricemia without signs of inflammatory arthritis and tophaceous disease, E79.1 – Lesch-Nyhan syndrome, E79.2 – Myoadenylate deaminase deficiency, E79.8 –…

The ICD-10 code for Aicardi-Goutières syndrome is E79.81.2026 ICD-10-CM Diagnosis Code E79.81 – Aicardi-Goutières syndrome Related ICD-10 Codes Parent code: E79 – Disorders of purine and pyrimidine metabolism Other codes in same category: E79.0 – Hyperuricemia without signs of inflammatory arthritis and tophaceous disease, E79.1 – Lesch-Nyhan syndrome, E79.2 – Myoadenylate deaminase deficiency, E79.8 –…

The ICD-10 code for Other disorders of purine and pyrimidine metabolism is E79.8.2026 ICD-10-CM Diagnosis Code E79.8 – Other disorders of purine and pyrimidine metabolism Related ICD-10 Codes Parent code: E79 – Disorders of purine and pyrimidine metabolism Other codes in same category: E79.0 – Hyperuricemia without signs of inflammatory arthritis and tophaceous disease, E79.1…

The ICD-10 code for Myoadenylate deaminase deficiency is E79.2.2026 ICD-10-CM Diagnosis Code E79.2 – Myoadenylate deaminase deficiency Related ICD-10 Codes Parent code: E79 – Disorders of purine and pyrimidine metabolism Other codes in same category: E79.0 – Hyperuricemia without signs of inflammatory arthritis and tophaceous disease, E79.1 – Lesch-Nyhan syndrome, E79.8 – Other disorders of…

The ICD-10 code for Lesch-Nyhan syndrome is E79.1.2026 ICD-10-CM Diagnosis Code E79.1 – Lesch-Nyhan syndrome Related ICD-10 Codes Parent code: E79 – Disorders of purine and pyrimidine metabolism Other codes in same category: E79.0 – Hyperuricemia without signs of inflammatory arthritis and tophaceous disease, E79.2 – Myoadenylate deaminase deficiency, E79.8 – Other disorders of purine…

The ICD-10 code for Hyperuricemia without signs of inflammatory arthritis and tophaceous disease is E79.0.2026 ICD-10-CM Diagnosis Code E79.0 – Hyperuricemia without signs of inflammatory arthritis and tophaceous disease Related ICD-10 Codes Parent code: E79 – Disorders of purine and pyrimidine metabolism Other codes in same category: E79.1 – Lesch-Nyhan syndrome, E79.2 – Myoadenylate deaminase…