Hereditary factor VIII deficiency
Billable / specificHCC V28 111
D66 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
- Classical hemophilia
- Deficiency factor VIII (with functional defect)
- Hemophilia NOS
- Hemophilia A
Excludes1
Not coded here — never report together with this code.
- factor VIII deficiency with vascular defect (D68.0-)
Excludes2
Not included here — may be reported together when both conditions 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)
Also known as
- Classical hemophilia
- Deficiency factor VIII (with functional defect)
- Hemophilia NOS
- Hemophilia A
- Arthritis, arthritic, due to or associated with, hemophilia
- Arthritis, arthritic, in hemophilia NEC
- Arthropathy, hemophilic NEC
- Arthropathy, in hemophilia NEC
- Deficiency, deficient, anti-hemophilic, factor
- Deficiency, deficient, anti-hemophilic, globulinNEC
- Deficiency, deficient, factor, VIII
- Disease, diseased, bleeder's
- Hemophilia
- Hemophilia, A
- Subhemophilia