D80.3
BillableSelective deficiency of immunoglobulin G [IgG] subclasses
Selective deficiency of immunoglobulin G [IgG] subclasses
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
- •autoimmune disease (systemic) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
Related Codes(9)
D80.0Hereditary hypogammaglobulinemia
D80.1Nonfamilial hypogammaglobulinemia
D80.2Selective deficiency of immunoglobulin A [IgA]
D80.4Selective deficiency of immunoglobulin M [IgM]
D80.5Immunodeficiency with increased immunoglobulin M [IgM]
D80.6Antibody defic w near-norm immunoglob or w hyperimmunoglob
D80.7Transient hypogammaglobulinemia of infancy
D80.8Other immunodeficiencies with predominantly antibody defects
D80.9Immunodeficiency with predominantly antibody defects, unsp
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(80)
SNOMED CT
- IgA deficiency29260007
- Immunoglobulin A deficiency29260007
- IgG subclass deficiency123785006
- Immunoglobin G subclass deficiency123785006
- Immunoglobulin G subclass deficiency123785006
- Selective IgG immunodeficiency190981001
- Selective immunoglobulin G deficiency190981001
- Immunoglobulin heavy chain deficiency234539005
- Immunoglobulin heavy chain deletion234539005
- IgG2 deficiency234546001
- Immunoglobulin G2 deficiency234546001
- Selective immunoglobulin G2 deficiency234546001
- Combined IgG2-IgG4 deficiency234547005
- Combined immunoglobulin G2 and G4 deficiency234547005
- IgG3 deficiency234548000
- Immunoglobulin G3 deficiency234548000
- IgG4 deficiency234549008
- Immunoglobulin G4 deficiency234549008
- IgG1 deficiency234550008
- Immunoglobulin G1 deficiency234550008
- Deficiency of immunoglobulin A with immunoglobulin G subclass deficiency840472009
- Immunoglobulin G deficiency12631000119106
- Immunoglobulin G deficiency due to monoclonal gammopathy of undetermined significance16894671000119102
- Immunoglobulin G deficiency due to multiple myeloma16894711000119103
UMLS
- DEFIC IGGC0162539
- Deficiencies, IgGC0162539
- Deficiency, IgGC0162539
- IGG DEFICC0162539
- IgG DeficienciesC0162539
- IgG DeficiencyC0162539
- IgG deficiencyC0162539
- IgG subclass deficiencyC0162539
- Immunoglobulin G deficiencyC0162539
- Immunoglobulin G deficiency (disorder)C0162539
- Selective IgG ImmunodeficiencyC0162539
- Selective IgG immunodeficiencyC0162539
- Selective IgG subclass deficiencyC0162539
- Selective Immunoglobulin G Subclass DeficiencyC0162539
- Selective deficiency of immunoglobulin G [IgG] subclassesC0162539
- Selective immunoglobulin G deficiencyC0162539
- Selective immunoglobulin G deficiency (disorder)C0162539
- deficiencies igg subclassC0162539
- igg deficienciesC0162539
- igg deficiencyC0162539
- igg subclass deficiencyC0162539
Clinical Terms
- Deficiency, IgG
- IgG4 deficiency
- Selective IgG Immunodeficiency
- DEFIC IGG
- IgG1 deficiency
- Selective immunoglobulin G2 deficiency
- Immunoglobulin G4 deficiency
- IgG Deficiencies
- deficiencies igg subclass
- IgA deficiency
- Deficiency of immunoglobulin A with immunoglobulin G subclass deficiency
- IgG2 deficiency
- Immunoglobulin G deficiency
- Selective IgG subclass deficiency
- Immunoglobulin heavy chain deficiency
- Immunoglobin G subclass deficiency
- IGG DEFIC
- IgG Deficiency
- Immunoglobulin G2 deficiency
- igg subclass deficiency
- Selective immunoglobulin G deficiency (disorder)
- Immunoglobulin G subclass deficiency
- Selective immunoglobulin G deficiency
- Combined IgG2-IgG4 deficiency
- Immunoglobulin G3 deficiency
- Immunoglobulin heavy chain deletion
- Immunoglobulin G deficiency due to monoclonal gammopathy of undetermined significance
- IgG3 deficiency
- Deficiencies, IgG
- Selective Immunoglobulin G Subclass Deficiency
- Immunoglobulin G1 deficiency
- Immunoglobulin G deficiency (disorder)
- Immunoglobulin A deficiency
- Combined immunoglobulin G2 and G4 deficiency
- Immunoglobulin G deficiency due to multiple myeloma
Frequently Asked Questions
What is the ICD-10 code for selective deficiency of immunoglobulin g [igg] subclasses?
The ICD-10-CM code for selective deficiency of immunoglobulin g [igg] subclasses is D80.3. The full clinical description is "Selective deficiency of immunoglobulin G [IgG] subclasses". D80.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D80.3 mean?
ICD-10-CM code D80.3 represents “Selective deficiency of immunoglobulin G [IgG] subclasses”. 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 D80.3 a billable code?
Yes, D80.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D80.3 in?
D80.3 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D80.3?
D80.3 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 D80.3 map to?
D80.3 maps to 13 SNOMED CT concepts: 234547005, 840472009, 29260007, 123785006, 234550008, and 8 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D80.3?
D80.3 is linked to 1 UMLS Concept Unique Identifier: C0162539. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D80.3 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like selective deficiency of immunoglobulin g [igg] subclasses 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 D80.3?
D80.3 maps to the ICD-11 code: 4A01.04 (Immunodeficiencies with isotype or light chain deficiencies with normal number of B cells).
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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.