Hemophilia B Brandenburg C4016497
A genetic variant of hemophilia B affecting blood clotting due to factor IX deficiency. Primarily affects males through inherited gene changes. Managed with clotting factor replacement to prevent and treat bleeding.
Key facts at a glance
- ICD-10
- D64.9
- ICD-11
- 3A00.0
- Body system
- hematologic
- Severity
- severe
- Chronic
- true
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy