Albinism, unspecified

This code signifies a congenital disorder characterized by a complete or partial absence of melanin pigment in the skin, hair, and/or eyes. It results from inherited defects in melanin production, leading to hypopigmentation.

Use this code when the medical record documents albinism without further specification of the type (e.g., oculocutaneous, ocular). This code is appropriate when the provider has diagnosed albinism but the specific genetic subtype or affected systems are not detailed.

• Only use this code when the type of albinism is truly unspecified in the documentation.
• Query the provider for more specific albinism types (e.g., E70.31 for Oculocutaneous albinism, E70.32 for Ocular albinism) if possible.
• Code any associated ocular conditions (e.g., nystagmus, photophobia, strabismus) separately.