| D62 | Acute posthemorrhagic anemia |
| D66 | Hereditary factor VIII deficiency |
| D67 | Hereditary factor IX deficiency |
| D68 | Other coagulation defects |
| D68.1 | Hereditary factor XI deficiency |
| D68.2 | Hereditary deficiency of other clotting factors |
| D68.311 | Acquired hemophilia |
| M25 | Other joint disorder, not elsewhere classified |
| M25.00 | Hemarthrosis, unspecified joint |
| M25.30 | Other instability, unspecified joint |
| M25.361 | Other instability, right knee |
| M36.2 | Hemophilic arthropathy |
| M79 | Other and unspecified soft tissue disorders, not elsewhere classified |
| M79.89 | Other specified soft tissue disorders |
| R04 | Hemorrhage from respiratory passages |
| R04.0 | Epistaxis |
| R23.3 | Spontaneous ecchymoses |
| R58 | Hemorrhage, not elsewhere classified |
| Z13.7 | Encounter for screening for genetic and chromosomal anomalies |
| Z14.0 | Hemophilia A carrier |
| Z14.01 | Asymptomatic hemophilia A carrier |
| Z14.02 | Symptomatic hemophilia A carrier |
| Z51.81 | Encounter for therapeutic drug level monitoring |
| Z79.899 | Other long term (current) drug therapy |
| Z83.2 | Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism |
| Z84.81 | Family history of carrier of genetic disease |