myICD10.com Logo
hemoglobin e disease

Medical Definition

A condition characterized by the presence of a variant of normal hemoglobin (hemoglobin e), which is caused by mutation(s) in the gene encoding the beta subunit of the hemoglobin molecule.
Related Codes (1)
Code
Description
Billable
Details
D58.2Other hemoglobinopathies
Type 1 Excludes (7)

Rows per page

Page 1 of 1