2008 ICD-9-CM Diagnosis Code 286.3 : Congenital deficiency of other clotting factors

Free ICD-9-CM Diagnosis Codes Lookup > 2008 > Diseases Of The Blood And Blood-Forming Organs 280-289 > Coagulation defects 286.* >

2008 ICD-9-CM Diagnosis Code 286.3

Congenital deficiency of other clotting factors

286.2

286.4

286.3 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Newer versions of 286.3: 2009 2010

Diagnosis Definition(s) Click to expand

Also applicable to/known as Click to expand

ICD-9-CM Volume 2 Index Entries That Refer To 286.3 Click to expand

Absence (organ or part) (complete or partial)

fibrinogen (congenital) 286.3
- acquired 286.6

Afibrinogenemia

286.3

acquired 286.6
congenital 286.3
postpartum 666.3

Defect, defective 759.9

fibrin polymerization (see also Defect, coagulation) 286.3
Hageman (factor) (see also Defect, coagulation) 286.3

Deficiency, deficient

accelerator globulin (Ac G) (blood) (see also Defect, coagulation) 286.3
AC globulin (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
activating factor (blood) (see also Defect, coagulation) 286.3
autoprothrombin
- I (see also Defect, coagulation) 286.3
- C (see also Defect, coagulation) 286.3
coagulation factor NEC 286.9
- specified type NEC 286.3
contact factor (see also Defect, coagulation) 286.3
factor (see also Defect, coagulation) 286.9
- I (congenital) (fibrinogen) 286.3
  - antepartum or intrapartum 641.3
    - affecting fetus or newborn 762.1
  - newborn, transient 776.3
  - postpartum 666.3
- II (congenital) (prothrombin) 286.3
- V (congenital) (labile) 286.3
- VII (congenital) (stable) 286.3
- X (congenital) (Stuart-Prower) 286.3
- XII (congenital) (Hageman) 286.3
- XIII (congenital) (fibrin stabilizing) 286.3
- hageman 286.3
fibrinase (see also Defect, coagulation) 286.3
fibrinogen (congenital) (see also Defect, coagulation) 286.3
- acquired 286.6
fibrin-stabilizing factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
glass factor (see also Defect, coagulation) 286.3
Hageman factor (congenital) (see also Defect, coagulation) 286.3
labile factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
laki-Lorand factor (see also Defect, coagulation) 286.3
proaccelerin (congenital) (see also Defect, congenital) 286.3
- acquired 286.7
proconvertin factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
prothrombin (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
Prower factor (see also Defect, coagulation) 286.3
SPCA (see also Defect, coagulation) 286.3
stable factor (congenital) (see also Defect, coagulation) 286.3
- acquired 286.7
Stuart (-Prower) factor (see also Defect, coagulation) 286.3
thrombokinase (see also Defect, coagulation) 286.3
- newborn 776.0

Disease, diseased - see also Syndrome

Hageman (congenital factor XII deficiency) (see also Defect, congenital) 286.3
Owren's (congenital) (see also Defect, coagulation) 286.3
Stuart's (congenital factor X deficiency) (see also Defect, coagulation) 286.3
Stuart-Prower (congenital factor X deficiency) (see also Defect, coagulation) 286.3

Dysfibrinogenemia (congenital) (see also Defect, coagulation)

286.3

Dysprothrombinemia (constitutional) (see also Defect, coagulation)

286.3

Fibrinogenopenia (congenital) (hereditary) (see also Defect, coagulation)

286.3

acquired 286.6

Fibrinopenia (hereditary) (see also Defect, coagulation)

286.3

acquired 286.6

Hageman factor defect, deficiency, or disease (see also Defect, coagulation)

286.3

Hypofibrinogenemia

286.3

acquired 286.6
congenital 286.3

Hypoproaccelerinemia (see also Defect, coagulation)

286.3

Hypoproconvertinemia (congenital) (see also Defect, coagulation)

286.3

Hypoprothrombinemia (congenital) (hereditary) (idiopathic) (see also Defect, coagulation)

286.3

acquired 286.7
newborn 776.3

Laki-Lorand factor deficiency (see also Defect, coagulation)

286.3

Owren's disease or syndrome (parahemophilia) (see also Defect, coagulation)

286.3

Parahemophilia (see also Defect, coagulation)

286.3

Stuart's disease (congenital factor X deficiency) (see also Defect, coagulation)

286.3

Stuart-Prower factor deficiency (congenital factor X deficiency) (see also Defect, coagulation)

286.3

Syndrome - see also Disease

Owren's (see also Defect, coagulation) 286.3

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