D68
Other coagulation defects
Choose the additional character
D68 needs more characters to be billable. Pick the specific code below.
- D68.0Von Willebrand diseaseMore levels
- D68.1Hereditary factor XI deficiencyBillable
- D68.2Hereditary deficiency of other clotting factorsBillable
- D68.3Hemorrhagic disorder due to circulating anticoagulantsMore levels
- D68.4Acquired coagulation factor deficiencyBillable
- D68.5Primary thrombophiliaMore levels
- D68.6Other thrombophiliaMore levels
- D68.8Other specified coagulation defectsBillable
- D68.9Coagulation defect, unspecifiedBillable
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
autoimmune disease (systemic) NOS (M35.9) certain conditions originating in the perinatal period (P00-P96) complications of pregnancy, childbirth and the puerperium (O00-O9A) congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) endocrine, nutritional and metabolic diseases (E00-E88) human immunodeficiency virus [HIV] disease (B20) injury, poisoning and certain other consequences of external causes (S00-T88) neoplasms (C00-D49) symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)