E70.320 Tyrosinase negative oculocutaneous albinismBillable ICD-10-CM code, FY2026. Acts as a Complication or Comorbidity (CC) as a secondary diagnosis.
Defines the logic of DRG(s) 642 in MDC 10.
270.2 Other disturbances of aromatic amino-acid metabolism (approximate)E72 Other disorders of amino-acid metabolism ("aromatic amino-acid metabolism (E70.-)")G11 Hereditary ataxia ("metabolic disorders (E70-E88)")G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")R79 Other abnormal findings of blood chemistry ("specific findings indicating disorder of amino-acid metabolism (E70-E72)")R79.83 Abnormal findings of blood amino-acid level ("disorders of amino-acid metabolism (E70-E72)")E70.310 X-linked ocular albinismE70.311 Autosomal recessive ocular albinismE70.318 Other ocular albinismE70.319 Ocular albinism, unspecifiedE70.32 Oculocutaneous albinismE70.320 Tyrosinase negative oculocutaneous albinism (this code)E70.321 Tyrosinase positive oculocutaneous albinismE70.328 Other oculocutaneous albinismE70.329 Oculocutaneous albinism, unspecifiedE70.33 Albinism with hematologic abnormalityE70.330 Chediak-Higashi syndrome