D68.2 Hereditary deficiency of other clotting factors

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

The following code(s) above D68.2 may contain annotation back-references that may be applicable to D68.2:

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)

Diagnosis Index

Absence

- Fibrinogen D68.2

Afibrinogenemia D68.8 - see also Defect, coagulation

- Congenital D68.2

Defect, Defective Q89.9

- Coagulation D68.9 - see also Deficiency, factor

-- Hereditary NEC D68.2

- Fibrin Polymerization D68.2

- Hageman D68.2

Deficiency, Deficient

- Accelerator Globulin D68.2

- AC Globulin D68.2

- Activating Factor D68.2

- Autoprothrombin

-- I D68.2

-- C D68.2

- Clotting Factor NEC D68.2 - see also Deficiency, factor

- Coagulation NOS D68.9

-- Clotting Factor NEC D68.2 - see also Deficiency, factor

- Contact Factor D68.2

- Factor - see also Deficiency, coagulation

-- Hageman D68.2

-- I D68.2

-- II D68.2

-- V D68.2

-- VII D68.2

-- X D68.2

-- XII D68.2

-- XIII D68.2

- Fibrin-stabilizing Factor D68.2

- Fibrinase D68.2

- Fibrinogen D68.2

- Glass Factor D68.2

- Hageman Factor D68.2

- Labile Factor D68.2

- Laki-Lorand Factor D68.2

- Proaccelerin D68.2

- Proconvertin Factor D68.2

- Prothrombin D68.2

- Prower Factor D68.2

- SPCA D68.2

- Stable Factor D68.2

- Stuart-Prower D68.2

- Thrombokinase D68.2

Disease, Diseased - see also Syndrome

- Hageman D68.2

- Stuart-Prower D68.2

- Stuart's D68.2

Dysfibrinogenemia D68.2

Fibrinogenopenia D68.8

- Congenital D68.2

Fibrinopenia D68.2

Hageman's Factor Defect, Deficiency Or Disease D68.2

Hypofibrinogenemia D68.8

- Congenital D68.2

Hypoproconvertinemia, Congenital D68.2

Hypoprothrombinemia D68.2

Owren's Disease Or Syndrome D68.2

Parahemophilia D68.2 - see also Defect, coagulation

Stuart Deficiency Disease D68.2

Stuart-Prower Factor Deficiency D68.2

Syndrome - see also Disease

- Owren's D68.2