E70.32 Oculocutaneous albinism

Non-billable header with 4 child codes.

Excludes1 (never code together)

• Chediak-Higashi syndrome (E70.330)
• Hermansky-Pudlak syndrome (E70.331)

Codes under E70.32

• E70.320 Tyrosinase negative oculocutaneous albinism
• E70.321 Tyrosinase positive oculocutaneous albinism
• E70.328 Other oculocutaneous albinism
• E70.329 Oculocutaneous albinism, unspecified

Code annotations containing back-references to E70.32

Back-references to E70

• Type 1 Excludes: E72 Other disorders of amino-acid metabolism ("aromatic amino-acid metabolism (E70.-)")
• Type 2 Excludes: G11 Hereditary ataxia ("metabolic disorders (E70-E88)")
• Code First: G63 Polyneuropathy in diseases classified elsewhere ("metabolic diseases (E70-E88)")
• Type 2 Excludes: G71 Primary disorders of muscles ("metabolic disorders (E70-E88)")
• Code First: H42 Glaucoma in diseases classified elsewhere ("specified metabolic disorder (E70-E88)")
• Type 2 Excludes: N25.0 Renal osteodystrophy ("metabolic disorders classifiable to E70-E88")
• Type 2 Excludes: N25.81 Secondary hyperparathyroidism of renal origin ("metabolic disorders classifiable to E70-E88")
• Type 1 Excludes: P59 Neonatal jaundice from other and unspecified causes ("jaundice due to inborn errors of metabolism (E70-E88)")
• Type 1 Excludes: R79 Other abnormal findings of blood chemistry ("specific findings indicating disorder of amino-acid metabolism (E70-E72)")
• Type 1 Excludes: R79.83 Abnormal findings of blood amino-acid level ("disorders of amino-acid metabolism (E70-E72)")

Nearby codes

• E70.31 Ocular albinism
• E70.310 X-linked ocular albinism
• E70.311 Autosomal recessive ocular albinism
• E70.318 Other ocular albinism
• E70.319 Ocular albinism, unspecified
• E70.32 Oculocutaneous albinism (this code)
• E70.320 Tyrosinase negative oculocutaneous albinism
• E70.321 Tyrosinase positive oculocutaneous albinism
• E70.328 Other oculocutaneous albinism
• E70.329 Oculocutaneous albinism, unspecified
• E70.33 Albinism with hematologic abnormality