Other specified albinism

This code signifies a rare, inherited disorder characterized by a partial or complete absence of melanin pigment in the skin, hair, and/or eyes, which does not fit into the more specific types of albinism. It encompasses various genetic mutations that lead to hypopigmentation, affecting visual development and increasing susceptibility to sun damage.

Use this code when documentation specifies a form of albinism that is not ocular albinism (E70.30), Hermansky-Pudlak syndrome (E70.31), or Chediak-Higashi syndrome (E70.32). This code is appropriate for other genetically confirmed or clinically diagnosed types of albinism that are not otherwise classified. Documentation should clearly state the specific type of albinism if known, or indicate "other specified albinism."

• Do not use this code for unspecified albinism; refer to E70.30 for such cases.
• Ensure the medical record differentiates this from ocular albinism, which primarily affects the eyes.
• Consider sequencing this code after any associated genetic conditions or syndromes if applicable.