icd-10 code for autosomal recessive ocular albinism

by Sammie Gulgowski MD 4 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.