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
2022 ICD-10-CM Diagnosis Code D69.0

2022 ICD-10-CM Diagnosis Code D69.0

Allergic purpura

2016

2017

2018

2019

2020

2021

2022

Billable/Specific Code

D69.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2022 edition of ICD-10-CM D69.0 became effective on October 1, 2021.
This is the American ICD-10-CM version of D69.0 - other international versions of ICD-10 D69.0 may differ.

Applicable To

Allergic vasculitis
Nonthrombocytopenic hemorrhagic purpura
Nonthrombocytopenic idiopathic purpura
Purpura anaphylactoid
Purpura Henoch(-Schönlein)
Purpura rheumatica
Vascular purpura

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 D69.0. 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.

thrombocytopenic hemorrhagic purpura (
ICD-10-CM Diagnosis Code D69.3
Immune thrombocytopenic purpura
Applicable To
- Hemorrhagic (thrombocytopenic) purpura
- Idiopathic thrombocytopenic purpura
- Tidal platelet dysgenesis
D69.3
)

The following code(s) above D69.0 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 D69.0:

D50-D89
2022 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
D69
ICD-10-CM Diagnosis Code D69
Purpura and other hemorrhagic conditions
Type 1 Excludes
- benign hypergammaglobulinemic purpura (D89.0)
- cryoglobulinemic purpura (D89.1)
- essential (hemorrhagic) thrombocythemia (D47.3)
- hemorrhagic thrombocythemia (D47.3)
- purpura fulminans (D65)
- thrombotic thrombocytopenic purpura (M31.19)
- Waldenström hypergammaglobulinemic purpura (D89.0)
Purpura and other hemorrhagic conditions

Approximate Synonyms

Glomerulonephritis due to henoch schonlein purpura
Henoch-schˆnlein purpura
Henoch-schönlein purpura
Purpura, henoch schonlein

Clinical Information

A systemic non-thrombocytopenic purpura caused by hypersensitivity vasculitis and deposition of iga-containing immune complexes within the blood vessels throughout the body, including those in the kidney (kidney glomerulus). Clinical symptoms include urticaria; erythema; arthritis; gastrointestinal hemorrhage; and renal involvement. Most cases are seen in children after acute upper respiratory infections.
A systemic, usually self-limited immune complex vasculitis, characterized by immunoglobulin a deposition in the small vessels and kidneys. It is manifested with small hemorrhages in the skin, gastrointestinal symptoms, arthritis, and nephropathy.
Disorder characterized by a vasculitic syndrome associated with exposure to an antigen such as a drug, infectious agent, or other foreign or endogenous substance. Its pathophysiology includes immune complex deposition and a wide range of skin lesions. Hypersensitivity or allergy is present in some but not all cases.

ICD-10-CM D69.0 is grouped within Diagnostic Related Group(s) (MS-DRG v39.0):

813 Coagulation disorders

Convert D69.0 to ICD-9-CM

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
2020 (effective 10/1/2019): No change
2021 (effective 10/1/2020): No change
2022 (effective 10/1/2021): No change

Code annotations containing back-references to D69.0:

Code First: M36.4

ICD-10-CM Diagnosis Code M36.4
Arthropathy in hypersensitivity reactions classified elsewhere
Code First
- underlying disease, such as:
- Henoch (-Schönlein) purpura (D69.0)
- serum sickness (T80.6-)
Type 1 Excludes: L95

ICD-10-CM Diagnosis Code L95
Vasculitis limited to skin, not elsewhere classified
Type 1 Excludes
- angioma serpiginosum (L81.7)
- Henoch(-Schönlein) purpura (D69.0)
- hypersensitivity angiitis (M31.0)
- lupus panniculitis (L93.2)
- panniculitis NOS (M79.3)
- panniculitis of neck and back (M54.0-)
- polyarteritis nodosa (M30.0)
- relapsing panniculitis (M35.6)
- rheumatoid vasculitis (M05.2)
- serum sickness (T80.6-)
- urticaria (L50.-)
- Wegener's granulomatosis (M31.3-)

Diagnosis Index entries containing back-references to D69.0:

Allergy, allergic (reaction) (to) T78.40
ICD-10-CM Diagnosis Code T78.40
Allergy, unspecified
Applicable To
Allergic reaction NOS
Hypersensitivity NOS
- purpura D69.0
Anaphylactic
- purpura D69.0
Arthritis, arthritic (acute) (chronic) (nonpyogenic) (subacute) M19.90
ICD-10-CM Diagnosis Code M19.90
Unspecified osteoarthritis, unspecified site
Applicable To
Arthrosis NOS
Arthritis NOS
Osteoarthritis NOS
- due to or associated with
  - Henoch- D69.0 (Schönlein)
- in (due to)
  - Henoch D69.0 (-Schönlein)
Arthropathy M12.9
- see also Arthritis
ICD-10-CM Diagnosis Code M12.9
Arthropathy, unspecified
- in (due to)
  - Henoch-Schönlein purpura D69.0
Disease, diseased - see also Syndrome
- Henoch D69.0 (-Schönlein) (purpura nervosa)
- Schönlein D69.0 (-Henoch) (purpura rheumatica)
Disorder (of) - see also Disease
- glomerular (in) N05.9
  ICD-10-CM Diagnosis Code N05.9
  Unspecified nephritic syndrome with unspecified morphologic changes
  2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
  - Henoch D69.0 (-Schönlein)
Glomerulonephritis N05.9
- see also Nephritis
ICD-10-CM Diagnosis Code N05.9
Unspecified nephritic syndrome with unspecified morphologic changes
- in (due to)
  - Henoch D69.0 (-Schönlein)
Henoch D69.0 (-Schönlein) disease or syndrome (purpura)
Peliosis (rheumatica) D69.0
Purpura D69.2
ICD-10-CM Diagnosis Code D69.2
Other nonthrombocytopenic purpura
Applicable To
Purpura NOS
Purpura simplex
Senile purpura
- hemorrhagic, hemorrhagica D69.3
  ICD-10-CM Diagnosis Code D69.3
  Immune thrombocytopenic purpura
  2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
  Applicable To
  Hemorrhagic (thrombocytopenic) purpura
  Idiopathic thrombocytopenic purpura
  Tidal platelet dysgenesis
  - not due to thrombocytopenia D69.0
- idiopathic (thrombocytopenic) D69.3
  ICD-10-CM Diagnosis Code D69.3
  Immune thrombocytopenic purpura
  2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
  Applicable To
  Hemorrhagic (thrombocytopenic) purpura
  Idiopathic thrombocytopenic purpura
  Tidal platelet dysgenesis
  - nonthrombocytopenic D69.0
- nonthrombocytopenic D69.2
  ICD-10-CM Diagnosis Code D69.2
  Other nonthrombocytopenic purpura
  2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code
  Applicable To
  Purpura NOS
  Purpura simplex
  Senile purpura
  - hemorrhagic D69.0
  - idiopathic D69.0
- abdominal D69.0
- allergic D69.0
- anaphylactoid D69.0
- arthritic D69.0
- autoimmune D69.0
- bacterial D69.0
- Henoch D69.0 (-Schönlein) (allergic)
- infectious D69.0
- malignant D69.0
- nervosa D69.0
- peliosis rheumatica D69.0
- rheumatica D69.0
- Schönlein D69.0 (-Henoch) (allergic)
- symptomatica D69.0
- toxic D69.0
- vascular D69.0
- visceral symptoms D69.0
Schönlein D69.0 (-Henoch) disease or purpura (primary) (rheumatic)
Syndrome - see also Disease
- Henoch-Schönlein D69.0
Toxicosis - see also Toxemia
- capillary, hemorrhagic D69.0
Vasculitis I77.6
ICD-10-CM Diagnosis Code I77.6
Arteritis, unspecified
Applicable To
Aortitis NOS
Endarteritis NOS
Type 1 Excludes
arteritis or endarteritis:
aortic arch (M31.4)
cerebral NEC (I67.7)
coronary (I25.89)
deformans (I70.-)
giant cell (M31.5, M31.6)
obliterans (I70.-)
senile (I70.-)
- allergic D69.0

ICD-10-CM Codes Adjacent To D69.0

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

D69.59 Other secondary thrombocytopenia

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

2022 ICD-10-CM Diagnosis Code D69.0

Allergic purpura

Immune thrombocytopenic purpura

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

Purpura and other hemorrhagic conditions

Arthropathy in hypersensitivity reactions classified elsewhere

Vasculitis limited to skin, not elsewhere classified

Allergy, unspecified

Unspecified osteoarthritis, unspecified site

Arthropathy, unspecified

Unspecified nephritic syndrome with unspecified morphologic changes

Unspecified nephritic syndrome with unspecified morphologic changes

Other nonthrombocytopenic purpura

Immune thrombocytopenic purpura

Immune thrombocytopenic purpura

Other nonthrombocytopenic purpura

Arteritis, unspecified