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ICD-10-CM Code D68.2
Hereditary deficiency of other clotting factors

Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
| ICD-10 from 2011 - 2016

D68.2 is a billable ICD code used to specify a diagnosis of hereditary deficiency of other clotting factors. A 'billable code' is detailed enough to be used to specify a medical diagnosis.

The ICD code D682 is used to code Congenital afibrinogenemia

Congenital afibrinogenemia is a rare, genetically inherited blood disorder in which the blood does not clot normally due to the lack of fibrinogen, a blood protein necessary for coagulation. This disorder is autosomal recessive, meaning that two unaffected parents can have a child with the disorder. The lack of fibrinogen expresses itself with excessive and, at times, uncontrollable bleeding.

Specialty: Hematology
MeSH Codes: D000347, D007020, D007020, D005177
ICD 9 Codes: 286.3, 286.3, 776.3, 286.3
Source: Wikipedia

Coding Notes for D68.2 Info for medical coders on how to properly use this ICD-10 code

Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
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)
Owren's disease
Proaccelerin deficiency

MS-DRG Mapping

  • DRG Group #813 - Coagulation disorders.

Related Concepts SNOMET-CT

  • Factor XIII inhibitor disorder (disorder)

ICD-10-CM Alphabetical Index References for 'D68.2 - Hereditary deficiency of other clotting factors'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code D68.2. Click on any term below to browse the alphabetical index.

Stuart deficiency disease(factor X) (D68.2)
Stuart-Prower factor deficiency(factor X) (D68.2)
Parahemophilia (D68.2) (see: Defect, coagulation)
Owren's disease or syndrome(parahemophilia) (D68.2)
Hageman's factor defect, deficiency or disease (D68.2)
Hypoproconvertinemia, congenital(hereditary) (D68.2)
Hypoprothrombinemia(congenital) (hereditary) (idiopathic) (D68.2)
Fibrinopenia(hereditary) (D68.2)
Dysfibrinogenemia(congenital) (D68.2)


Congenital deficiency of other clotting factors (exact match)

This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 286.3 was previously used, D68.2 is the appropriate modern ICD10 code.

Parent Code: D68 - Other coagulation defects

** This Document Provided By ICD.Codes **
Source: http://icd.codes/icd10cm/D682