AutoICD API

D82.0

Billable

Wiskott-Aldrich syndrome

Wiskott-Aldrich syndrome

Status

Billable / Specific

Block

D80-D89

Parent Code

D82

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Immunodeficiency with thrombocytopenia and eczema

Includes

Conditions included under this code

  • defects in the complement system
  • immunodeficiency disorders, except human immunodeficiency virus [HIV] disease
  • sarcoidosis

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(6)
D82.1

Di George's syndrome

BillableD82.2

Immunodeficiency with short-limbed stature

BillableD82.3

Immunodef fol heredit defctv response to Epstein-Barr virus

BillableD82.4

Hyperimmunoglobulin E [IgE] syndrome

BillableD82.8

Immunodeficiency associated with oth major defects

BillableD82.9

Immunodeficiency associated with major defect, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

3B62.0YOther specified inherited qualitative platelet defectsequivalentPrimary
Also Known As / Clinical Terms(74)

SNOMED CT

UMLS

Clinical Terms

  • Wiskott Syndrome
  • ECZEMA-THROMBOCYTOPENIA-IMMUNODEFICIENCY SYNDROME
  • WISKOTT-ALDRICH SYNDROME 1
  • Wiskott-Aldrich autosomal dominant variant syndrome
  • ALDRICH SYNDROME
  • eczema thromocytopenia immunodeficiency syndrome
  • Immunodeficiency with thrombocytopenia and eczema
  • eczema thromocytopenia diarrhea syndrome
  • Eczema-Thrombocytopenia-Immunodeficiency Syndromes
  • Eczema Thrombocytopenia Immunodeficiency Syndrome
  • Eczema, thrombocytopenia, immunodeficiency syndrome
  • Storage pool deficiency
  • wiskott aldrich syndrome
  • IMD2
  • aldrich syndrome wiskott
  • Immunodeficiency 2
  • Immunodeficiency 2s
  • Immunodeficiency with major anomalies
  • WAS1
  • Dense body defect
  • Wiskott Syndromes
  • eczema thromocytopenia syndrome
  • WAS
  • WAS - Wiskott-Aldrich syndrome
  • Wiskott-Aldrich syndrome (disorder)
  • Immunodeficiency associated with multiple organ system abnormalities
Frequently Asked Questions
What is the ICD-10 code for wiskott-aldrich syndrome?

The ICD-10-CM code for wiskott-aldrich syndrome is D82.0. The full clinical description is "Wiskott-Aldrich syndrome". D82.0 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D82.0 mean?

ICD-10-CM code D82.0 represents “Wiskott-Aldrich syndrome”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.

Is D82.0 a billable code?

Yes, D82.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D82.0 in?

D82.0 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D82.0?

D82.0 has Excludes1 notes indicating codes that cannot be used together with it, including: autoimmune disease (systemic) NOS (M35.9); functional disorders of polymorphonuclear neutrophils (D71); human immunodeficiency virus [HIV] disease (B20); and 1 more.

What SNOMED CT codes does D82.0 map to?

D82.0 maps to 5 SNOMED CT concepts: 36070007, 234474009, 234641000, 234631003, 403837005. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D82.0?

D82.0 is linked to 1 UMLS Concept Unique Identifier: C0043194. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D82.0 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like wiskott-aldrich syndrome affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of D82.0?

D82.0 maps to the ICD-11 code: 3B62.0Y (Other specified inherited qualitative platelet defects).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.