Sickle Cell Hemoglobin C Disease C0019034
Sickle cell hemoglobin C disease is a blood disorder where someone inherits hemoglobin S and hemoglobin C genes, causing mild to moderate anemia. Most people have a good outlook with routine medical monitoring.
Key facts at a glance
- ICD-10
- D64.9
- ICD-11
- 3A00.0
- Body system
- hematologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Warning signs - seek immediate care
Vision loss
Fatigue
(hematologic)Generalized symptoms
(hematologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Vaso-occlusive pain crisis
(hematologic)Splenomegaly
(hematologic)Medication Comparisons
Compare medications used to treat Sickle Cell Hemoglobin C Disease C0019034. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy