Kodex

Code

D68.2

Hereditary deficiency of other clotting factors

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Hierarchy

D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
- D65-D69 Coagulation defects, purpura and other hemorrhagic conditions (D65-D69)
  - D68 Other coagulation defects
    - D68.0 Von Willebrand disease
    - D68.1 Hereditary factor XI deficiency
    - D68.2 Hereditary deficiency of other clotting factors
    - D68.3 Hemorrhagic disorder due to circulating anticoagulants
    - D68.4 Acquired coagulation factor deficiency
    - D68.5 Primary thrombophilia
    - D68.6 Other thrombophilia
    - D68.8 Other specified coagulation defects
    - D68.9 Coagulation defect, unspecified

Inclusion Terms

D68.2

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

Excludes 1

R79.1 Abnormal coagulation profile

Excludes 2

coagulation defects complicating abortion or ectopic or molar pregnancy (O00-O07, O08.1)
- O08.1 Delayed or excessive hemorrhage following ectopic and molar pregnancy
coagulation defects complicating pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)
- O45.0 Premature separation of placenta with coagulation defect
- O46.0 Antepartum hemorrhage with coagulation defect
- O67.0 Intrapartum hemorrhage with coagulation defect
- O72.3 Postpartum coagulation defects

autoimmune disease (systemic) NOS (M35.9)
- M35.9 Systemic involvement of connective tissue, unspecified
P00-P96 Certain conditions originating in the perinatal period (P00-P96)
complications of pregnancy, childbirth and the puerperium (O00-O9A)
- O00-O9A Pregnancy, childbirth and the puerperium (O00-O9A)
Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
endocrine, nutritional and metabolic diseases (E00-E88)
B20 Human immunodeficiency virus [HIV] disease
S00-T88 Injury, poisoning and certain other consequences of external causes (S00-T88)
C00-D49 Neoplasms (C00-D49)
symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)