AutoICD API

D83.8

Billable

Other common variable immunodeficiencies

Other common variable immunodeficiencies

Status

Billable / Specific

Block

D80-D89

Parent Code

D83

ICD-11 Mapping

1 equivalent

Coding Notes

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(4)
D83.0

Com variab immunodef w predom abnlt of B-cell nums & functn

BillableD83.1

Com variab immunodef w predom immunoreg T-cell disorders

BillableD83.2

Common variable immunodef w autoantibodies to B- or T-cells

BillableD83.9

Common variable immunodeficiency, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

4A01.0YOther specified immunodeficiencies with predominantly antibody defectsequivalentPrimary
Also Known As / Clinical Terms(113)

SNOMED CT

UMLS

Clinical Terms

  • Autosomal dominant CVID (combined variable immunodeficiency) due to IRF2BP2 deficiency
  • Autosomal dominant combined variable immunodeficiency due to SEC61 translocon subunit alpha 1 mutation
  • X-linked common variable immune deficiency due to CIN85 deficiency
  • Autosomal dominant combined variable immunodeficiency due to TWEAK deficiency
  • Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation
  • Autosomal recessive combined variable immunodeficiency due to BAFF-R mutation
  • Autosomal recessive CVID (combined variable immunodeficiency) due to ARHGEF1 deficiency
  • Autosomal recessive common variable immunodeficiency due to CR2 mutation
  • Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation
  • Autosomal recessive combined variable immunodeficiency due to PIK3CG deficiency
  • Autosomal recessive CVID (common variable immunodeficiency) due to CD21 deficiency
  • Autosomal recessive combined variable immunodeficiency due to Rho guanine nucleotide exchange factor 1 mutation
  • Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation
  • Autosomal recessive CVID (combined variable immunodeficiency) due to PIK3CG deficiency
  • Autosomal dominant combined variable immunodeficiency due to NFKB1 deficiency
  • Autosomal recessive common variable immunodeficiency due to CD21 deficiency
  • Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency
  • Autosomal dominant combined variable immunodeficiency due to SEC61A1 deficiency
  • CVID (common variable immunodeficiency) due to TNFRSF13B gene mutation
  • Autosomal recessive common variable immunodeficiency due to CD20 mutation
  • Autosomal dominant combined variable immunodeficiency due to IRF2BP2 deficiency
  • CVID (common variable immunodeficiency) due to TACI deficiency
  • Autosomal dominant combined variable immunodeficiency due to TWEAK mutation
  • Autosomal dominant combined variable immunodeficiency due to tumour necrosis factor-like weak inducer of apoptosis mutation
  • Autosomal dominant CVID (combined variable immunodeficiency) due to SEC61A1 deficiency
  • Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation
  • X-linked common variable immunodeficiency due to SH3KBP1 deficiency
  • Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency
  • Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation
  • Autosomal recessive CVID (combined variable immunodeficiency) due to TNFRSF13C mutation
  • Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation
  • Autosomal dominant combined variable immunodeficiency due to SEC61A1 mutation
  • Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation
  • Autosomal dominant combined variable immunodeficiency due to IRF2BP2 mutation
  • Autosomal recessive CVID (common variable immunodeficiency) due to CD20 deficiency
  • Autosomal recessive common variable immunodeficiency due to POU2AF1 mutation
  • Autosomal recessive CVID (common variable immunodeficiency) due to RAC2 mutation
  • Autosomal recessive common variable immunodeficiency due to MS4A1 mutation
  • Autosomal recessive common variable immunodeficiency due to RAC2 deficiency
  • Common variable immunodeficiency due to transmembrane activator and calcium-modulator and cyclophilin ligand interactor deficiency
  • Autosomal recessive common variable immunodeficiency due to CD21 mutation
  • Autosomal dominant CVID (combined variable immunodeficiency) due to NFKB1 deficiency
  • Autosomal recessive combined variable immunodeficiency due to BAFF-R deficiency
  • Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation
  • Autosomal recessive combined variable immunodeficiency due to phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma mutation
  • X-linked common variable immunodeficiency due to SH3 domain containing kinase binding protein 1 deficiency
  • Autosomal recessive common variable immunodeficiency due to BOB1 deficiency
  • Autosomal recessive common variable immunodeficiency due to membrane spanning 4-domains A1 mutation
  • Autosomal recessive common variable immunodeficiency due to CD20 deficiency
  • Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation
  • Autosomal recessive combined variable immunodeficiency due to ARHGEF1 deficiency
  • Common variable immunodeficiency due to TACI deficiency
  • Autosomal recessive CVID (common variable immunodeficiency) due to CD81 deficiency
  • Autosomal recessive common variable immunodeficiency due to CD81 deficiency
  • Autosomal recessive common variable immunodeficiency due to RAC2 mutation
  • Autosomal dominant CVID (combined variable immunodeficiency) due to TNFSF12 mutation
Frequently Asked Questions
What is the ICD-10 code for other common variable immunodeficiencies?

The ICD-10-CM code for other common variable immunodeficiencies is D83.8. The full clinical description is "Other common variable immunodeficiencies". D83.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D83.8 mean?

ICD-10-CM code D83.8 represents “Other common variable immunodeficiencies”. 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 D83.8 a billable code?

Yes, D83.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D83.8 in?

D83.8 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D83.8?

D83.8 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).

What SNOMED CT codes does D83.8 map to?

D83.8 maps to 14 SNOMED CT concepts: 1354420003, 1354416002, 1354480001, 1352026003, 1354472008, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D83.8?

D83.8 is linked to 1 UMLS Concept Unique Identifier: C0477327. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D83.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other common variable immunodeficiencies 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 D83.8?

D83.8 maps to the ICD-11 code: 4A01.0Y (Other specified immunodeficiencies with predominantly antibody 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.