icd-10 code for autosomal recessive ocular albinism

by Sammie Gulgowski MD 10 min read

E70.311

Index to Diseases and Injuries

The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code (s). The following references for the code E70.311 are found in the index:

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

Convert E70.311 to ICD-9 Code

The General Equivalency Mapping (GEM) crosswalk indicates an approximate mapping between the ICD-10 code E70.311 its ICD-9 equivalent. The approximate mapping means there is not an exact match between the ICD-10 code and the ICD-9 code and the mapped code is not a precise representation of the original code.

Information for Patients

Some eye problems are minor and don't last long. But some can lead to a permanent loss of vision.

The ICD code E703 is used to code Piebaldism

Piebaldism is a rare autosomal dominant disorder of melanocyte development.:867 Common characteristics include a congenital white forelock, scattered normal pigmented and hypopigmented macules and a triangular shaped depigmented patch on the forehead.

ICD-10-CM Alphabetical Index References for 'E70.31 - Ocular albinism'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E70.31. Click on any term below to browse the alphabetical index.