Hereditary deficiency of other clotting factors
Billable / specificHCC V28 112
D68.2 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- 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
Excludes1
Not coded here — never report together with this code.
Excludes2
Not included here — may be reported together when both conditions exist.
- autoimmune disease (systemic) NOS (M35.9) (from D68)
- certain conditions originating in the perinatal period (P00-P96) (from D68)
- complications of pregnancy, childbirth and the puerperium (O00-O9A) (from D68)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) (from D68)
- endocrine, nutritional and metabolic diseases (E00-E88) (from D68)
- human immunodeficiency virus [HIV] disease (B20) (from D68)
- injury, poisoning and certain other consequences of external causes (S00-T88) (from D68)
- neoplasms (C00-D49) (from D68)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94) (from D68)
- coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1) (from D68)
- coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3) (from D68)
Also known as
- 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
- Absence, fibrinogen
- Afibrinogenemia, congenital
- Defect, defective, coagulation, hereditary NEC
- Defect, defective, fibrin polymerization
- Defect, defective, Hageman
- Deficiency, deficient, accelerator globulin
- Deficiency, deficient, AC globulin
- Deficiency, deficient, activating factor
- Deficiency, deficient, autoprothrombin, I
- Deficiency, deficient, autoprothrombin, C
- Deficiency, deficient, clotting factor NEC
- Deficiency, deficient, coagulation NOS, clotting factor NEC
Parent code
- D68Other coagulation defectsHeader
Related codes
- D68.0Von Willebrand diseaseHeader
- D68.1Hereditary factor XI deficiencyBillable
- D68.3Hemorrhagic disorder due to circulating anticoagulantsHeader
- D68.4Acquired coagulation factor deficiencyBillable
- D68.5Primary thrombophiliaHeader
- D68.6Other thrombophiliaHeader
- D68.8Other specified coagulation defectsBillable
- D68.9Coagulation defect, unspecifiedBillable