×

FREE Find-A-Code Demonstration

All Attendees Get Free 2-Week Trial Access!

 

The Right Code - Right Now™

 

NEW! Introducing

Find‑A‑Code's new Ai assistant

and

other NEW Find‑A‑Code features!

 

Register now for this free live demo Thursday, February 12 @ 1:00pm Eastern. See how Find-A-Code's workflow matches yours, putting the most important information right at your fingertips in an easy-to-use format.

 

Why Find-A-Code?

• Complete Code Sets: CPT®, ICD-10-CM, HCPCS and more
• The Easiest, Fastest, and Most Accurate NCCI Validation
• Complete NCD/LCD Policies
• NEW AI features that make you a better coder

All The Features You Need

• AHA Coding Clinic® integration
• RVUs with facility factors
• UCR fees by location
• Commercial payer policies
• Common Language Descriptions (CLDs)
• Many, many more!

FREE DEMO - Register Now

close

3A51.9 Haemoglobin O disease

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2025-01

A disease caused by the bi-parental inheritance of the gene that encodes for haemoglobin O. This disease is characterised by abnormal structure of one of the globin chains of the haemoglobin molecule. This disease may present with mild haemolytic anaemia, increased risk for gallstones, enlarged spleen, episodes of joint pain, and increased risk of infection. This disease is confirmed by identification of the haemoglobin O gene by genetic testing.

synonyms

• Haemoglobin O disease
• Arab disease

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