ICD-10-CM Codes
D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
D65-D69 Coagulation defects, purpura and other hemorrhagic conditions
D69- Purpura and other hemorrhagic conditions

2018/2019 ICD-10-CM Diagnosis Code D69

Purpura and other hemorrhagic conditions

2016

2017

2018

2019

Non-Billable/Non-Specific Code

D69 should not be used for reimbursement purposes as there are multiple codes below it that contain a greater level of detail.
The 2018/2019 edition of ICD-10-CM D69 became effective on October 1, 2018.
This is the American ICD-10-CM version of D69 - other international versions of ICD-10 D69 may differ.

Type 1 Excludes

Type 1 Excludes Help

A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as D69. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

benign hypergammaglobulinemic purpura (
ICD-10-CM Diagnosis Code D89.0
Polyclonal hypergammaglobulinemia
Applicable To
- Benign hypergammaglobulinemic purpura
- Polyclonal gammopathy NOS
D89.0
)
cryoglobulinemic purpura (
ICD-10-CM Diagnosis Code D89.1
Cryoglobulinemia
Applicable To
- Cryoglobulinemic purpura
- Cryoglobulinemic vasculitis
- Essential cryoglobulinemia
- Idiopathic cryoglobulinemia
- Mixed cryoglobulinemia
- Primary cryoglobulinemia
- Secondary cryoglobulinemia
D89.1
)
essential (hemorrhagic) thrombocythemia (
ICD-10-CM Diagnosis Code D47.3
Essential (hemorrhagic) thrombocythemia
Applicable To
- Essential thrombocytosis
- Idiopathic hemorrhagic thrombocythemia
D47.3
)
hemorrhagic thrombocythemia (
ICD-10-CM Diagnosis Code D47.3
Essential (hemorrhagic) thrombocythemia
Applicable To
- Essential thrombocytosis
- Idiopathic hemorrhagic thrombocythemia
D47.3
)
purpura fulminans (
ICD-10-CM Diagnosis Code D65
Disseminated intravascular coagulation [defibrination syndrome]
Applicable To
- Afibrinogenemia, acquired
- Consumption coagulopathy
- Diffuse or disseminated intravascular coagulation [DIC]
- Fibrinolytic hemorrhage, acquired
- Fibrinolytic purpura
- Purpura fulminans
Type 1 Excludes
- disseminated intravascular coagulation (complicating):
- abortion or ectopic or molar pregnancy (O00-O07, O08.1)
- in newborn (P60)
- pregnancy, childbirth and the puerperium (O45.0, O46.0, O67.0, O72.3)
D65
)
thrombotic thrombocytopenic purpura (
ICD-10-CM Diagnosis Code M31.1
Thrombotic microangiopathy
Applicable To
- Thrombotic thrombocytopenic purpura
M31.1
)
Waldenström hypergammaglobulinemic purpura (
ICD-10-CM Diagnosis Code D89.0
Polyclonal hypergammaglobulinemia
Applicable To
- Benign hypergammaglobulinemic purpura
- Polyclonal gammopathy NOS
D89.0
)

The following code(s) above D69 contain annotation back-references

Annotation Back-References

In this context, annotation back-references refer to codes that contain:

Applicable To annotations, or
Code Also annotations, or
Code First annotations, or
Excludes1 annotations, or
Excludes2 annotations, or
Includes annotations, or
Note annotations, or
Use Additional annotations

that may be applicable to D69:

D50-D89
2019 ICD-10-CM Range D50-D89
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
Type 2 Excludes
- 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)
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Code History

2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
2017 (effective 10/1/2016): No change
2018 (effective 10/1/2017): No change
2019 (effective 10/1/2018): No change

Code annotations containing back-references to D69:

Type 1 Excludes: R23.3

ICD-10-CM Diagnosis Code R23.3
Spontaneous ecchymoses
Applicable To
- Petechiae
Type 1 Excludes
- ecchymoses of newborn (P54.5)
- purpura (D69.-)

ICD-10-CM Codes Adjacent To D69

D68.5 Primary thrombophilia

D68.51 Activated protein C resistance

D68.52 Prothrombin gene mutation

D68.59 Other primary thrombophilia

D68.6 Other thrombophilia

D68.61 Antiphospholipid syndrome

D68.62 Lupus anticoagulant syndrome

D68.69 Other thrombophilia

D68.8 Other specified coagulation defects

D68.9 Coagulation defect, unspecified

D69 Purpura and other hemorrhagic conditions

D69.0 Allergic purpura

D69.1 Qualitative platelet defects

D69.2 Other nonthrombocytopenic purpura

D69.3 Immune thrombocytopenic purpura

D69.4 Other primary thrombocytopenia

D69.41 Evans syndrome

D69.42 Congenital and hereditary thrombocytopenia purpura

D69.49 Other primary thrombocytopenia

D69.5 Secondary thrombocytopenia

D69.51 Posttransfusion purpura

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

2018/2019 ICD-10-CM Diagnosis Code D69

Purpura and other hemorrhagic conditions

Polyclonal hypergammaglobulinemia

Cryoglobulinemia

Essential (hemorrhagic) thrombocythemia

Essential (hemorrhagic) thrombocythemia

Disseminated intravascular coagulation [defibrination syndrome]

Thrombotic microangiopathy

Polyclonal hypergammaglobulinemia

Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Spontaneous ecchymoses