3B50
Inherited fibrinolytic defects
Inherited fibrinolytic defects
Child Codes (4)
Frequently Asked Questions
What is the ICD-11 code for inherited fibrinolytic defects?
The ICD-11 code for inherited fibrinolytic defects is 3B50. The full clinical description is "Inherited fibrinolytic defects".
What does ICD-11 code 3B50 mean?
ICD-11 code 3B50 represents “Inherited fibrinolytic defects”. It is classified under Chapter 3: Diseases of the Blood or Blood-Forming Organs.
What chapter is 3B50 in?
3B50 is in Chapter 3: Diseases of the Blood or Blood-Forming Organs (codes 3A00-3C9Z).
What is the ICD-10 equivalent of ICD-11 code 3B50?
There is no direct ICD-10 mapping available for 3B50 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-10. Use the ICD-11 to ICD-10 converter to search for related codes.
What is the difference between ICD-10 and ICD-11?
ICD-11 is the latest revision of the WHO's International Classification of Diseases, succeeding ICD-10. Key differences include: a fully digital-first design, new chapters for sleep-wake disorders, sexual health, and traditional medicine, improved coding for rare diseases, and better integration with electronic health records through extension codes.
What are the subcategories under 3B50?
3B50 has 4 child codes, including: 3B50.0 (Congenital alpha-2 antiplasmin deficiency), 3B50.1 (Congenital plasminogen activator inhibitor type 1 deficiency), 3B50.Y (Other specified inherited fibrinolytic defects), 3B50.Z (Inherited fibrinolytic defects, unspecified).
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