E70.30

HCC Category Mapping

What This Code Means

A genetic condition where the body produces little to no melanin (pigment), resulting in very light skin, hair, and eyes, but the specific type is not specified.

Coding Tips

• •Albinism has multiple subtypes; review clinical documentation to determine if ocular or oculocutaneous albinism is present
• •Document any associated vision problems or skin complications for complete coding

Clinical Significance

Albinism, unspecified, indicates a genetic condition with absent or significantly reduced melanin production, but the specific type (ocular, oculocutaneous, or with hematologic abnormality) has not been determined. Patients face increased risks of skin cancer from ultraviolet exposure, significant visual impairment including nystagmus and photophobia, and social stigmatization, requiring multidisciplinary management including dermatologic surveillance and ophthalmologic care.

Documentation Requirements

• ✓Documentation should describe the extent of pigment loss (skin only, eyes only, or both), visual acuity findings, nystagmus assessment, and skin examination results.
• ✓The provider should specify whether this is ocular or oculocutaneous albinism and document any hematologic abnormalities.
• ✓Genetic testing results and family history should be included.
• ✓Skin cancer screening frequency and sun protection counseling should be noted.

Commonly Confused Codes