NEW! - AMA CPT Advanced Coding Pack

×

Unlock the full potential of your medical coding capabilities with the CPT® Advanced Coding Pack from the American Medical Association (AMA). Designed for professional medical coders, auditors, and billers like you, this comprehensive suite of resources provides everything you need to navigate the complexities of the CPT code set with confidence and precision.

 

Advanced Coding Pack includes:

1. CPT Assistant - Newsletter with official education and guidance
2. CPT Knowledge Base - Commonly asked coding questions answered by the experts
3. CPT Vignettes - Comprehensive clinical examples.

Add to your Find-A-Code subscription for $300 / person

Learn More and Subscribe

close

3A10.2 Hereditary elliptocytosis

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Hereditary elliptocytosis is a group of rare conditions caused by abnormalities in the red cell cytoskeleton and marked by the presence on blood smears of numerous elliptical red blood cells, called elliptocytes. Clinical presentations are highly heterogeneous ranging from asymptomatic forms to more severe forms associated with variable anaemia, from moderate to severe and with pyropoikilocytosis including fragmented red cells, microelliptocytes and microspherocytes.

inclusions

• Common hereditary elliptocytosis
• Homozygous hereditary elliptocytosis
• Spherocytic elliptocytosis
• Hereditary pyropoikilocytosis

synonyms

• Hereditary elliptocytosis
• congenital ovalocytosis
• elliptocytosis
• ovalocytosis
• Hereditary elliptocytosis with infantile poikilocytosis
• congenital elliptocytosis
• hereditary ovalocytosis
• oval erythrocytosis
• HE - [hereditary elliptocytosis]
• elliptocytosis anaemia
• Common hereditary elliptocytosis
• Common heterozygous hereditary elliptocytosis
• Homozygous hereditary elliptocytosis
• Spherocytic elliptocytosis
• Hereditary pyropoikilocytosis

Thank you for choosing Find-A-Code, please Sign In to remove ads.