ICD-10-CM Diagnosis Code (2025)
Official Description for D68.2
Hereditary deficiency of other clotting factors
Coding Notes & Guidelines for D68.2
Inclusion Terms
- AC globulin deficiency
- Congenital afibrinogenemia
- Deficiency of factor I [fibrinogen]
- Deficiency of factor II [prothrombin]
- Deficiency of factor V [labile]
- Deficiency of factor VII [stable]
- Deficiency of factor X [Stuart-Prower]
- Deficiency of factor XII [Hageman]
- Deficiency of factor XIII [fibrin stabilizing]
- Dysfibrinogenemia (congenital)
- Hypoproconvertinemia
- Owren's disease
- Proaccelerin deficiency
Parent Code (Less Specific):
About ICD-10-CM Code D68.2 (Hereditary deficiency of other clotting factors)
ICD-10-CM code D68.2 is a billable or specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM D68.2 became effective on October 1, 2024.
This page provides detailed information about D68.2 - Hereditary deficiency of other clotting factors. It includes common terminology, coding guidelines such as "Includes," "Excludes1," and "Excludes2" notes, and information on required 7th characters. Utilizing this information correctly is essential for accurate medical coding and claims submission for conditions like Hereditary deficiency of other clotting factors.