Skip to content

E70.319

Billable

Ocular albinism, unspecified

HCC Category Mapping

V24HCC 23Other Significant Endocrine and Metabolic Disorders
0.230
ESRDHCC 23Other Significant Endocrine and Metabolic Disorders
0.000
RxHCCHCC 43Other Significant Endocrine and Metabolic Disorders
0.000

What This Code Means

A genetic condition affecting only the eyes with reduced melanin production causing vision problems, but the specific inheritance pattern or type is not identified.

Coding Tips

  • This is the least specific ocular albinism code; query provider for inheritance pattern or specific type if possible
  • Document all vision-related complications separately

Clinical Significance

Ocular albinism, unspecified, indicates reduced melanin production limited to the eyes without skin involvement, where the specific inheritance pattern or genetic type has not been determined. This condition causes visual impairment, nystagmus, and photophobia, and the unspecified designation typically reflects incomplete genetic evaluation rather than a truly indeterminate condition.

Documentation Requirements

  • Documentation should include ophthalmologic examination findings demonstrating reduced ocular pigmentation, visual acuity measurements, nystagmus characterization, and iris transillumination results.
  • The provider should document that skin pigmentation is normal or near-normal.
  • If genetic testing has been performed, results should guide assignment of a more specific code.
  • If testing has not been done, document the reason and plan for evaluation.

Commonly Confused Codes

Code Hierarchy

Open E70.319 in the Interactive Encoder

See full code details, AI coding tips, HCC mappings, and related codes in our interactive encoder. Start your 14-day Pro trial — no credit card required.