D80.8
BillableOther immunodeficiencies with predominantly antibody defects
Other immunodeficiencies with predominantly antibody defects
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Kappa light chain deficiency
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]
D80.3Selective deficiency of immunoglobulin G [IgG] subclasses
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
D80.9Immunodeficiency 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(76)
SNOMED CT
- Alopecia totalis19754005
- Total alopecia areata19754005
- Kappa light chain disease45841007
- Light chain disease51319002
- Lambda light chain disease66876008
- Immune defect71922006
- Immunologic defect71922006
- Humoral immune defect103075007
- Humoral immunity deficiency103075007
- Humoural immune defect103075007
- Humoural immunity deficiency103075007
- Predominantly B-cell defect103075007
- Abnormal beta globulin level127390005
- Beta globulin level outside reference range127390005
- Hypobetaglobulinaemia129649008
- Hypobetaglobulinemia129649008
- Selective immunoglobulin dysfunction234535004
- Immunoglobulin heavy chain deficiency234539005
- Immunoglobulin heavy chain deletion234539005
- Selective IgE deficiency234540007
- Selective immunoglobulin E deficiency234540007
- Selective IgD deficiency234541006
- Selective immunoglobulin D deficiency234541006
- Immunoglobulin light chain deficiency234543009
- Functional antibody defect234556002
- Specific antibody deficiency234556002
- Specific immunoglobulin response defect234556002
- Primary immunoglobulin catabolism abnormality234564008
- Kappa light chain deficiency449187006
- Lambda light chain deficiency449384005
- Disorder of kidney due to kappa light chain disease449408005
- Kappa light chain nephropathy449408005
- Disorder of kidney due to lambda light chain disease449409002
- Lambda light chain nephropathy449409002
- Alopecia antibody deficiency783205005
- Ipp Gelfand syndrome783205005
UMLS
Clinical Terms
- Disorder of kidney due to lambda light chain disease
- Specific antibody deficiency
- Immunoglobulin light chain deficiency
- Hypobetaglobulinemia
- Alopecia totalis
- Kappa light chain deficiency
- Primary immunoglobulin catabolism abnormality
- Selective immunoglobulin dysfunction
- Abnormal beta globulin level
- Kappa light chain disease
- Immunoglobulin heavy chain deficiency
- Kappa light chain nephropathy
- Selective immunoglobulin E deficiency
- Beta globulin level outside reference range
- Functional antibody defect
- Humoral immune defect
- Humoural immune defect
- Immunologic defect
- Immune defect
- Lambda light chain deficiency
- Selective IgD deficiency
- Selective IgE deficiency
- Selective immunoglobulin D deficiency
- Kappa light chain deficiency (disorder)
- Immunoglobulin heavy chain deletion
- Alopecia antibody deficiency
- Humoral immunity deficiency
- Total alopecia areata
- Disorder of kidney due to kappa light chain disease
- Humoural immunity deficiency
- Hypobetaglobulinaemia
- Lambda light chain disease
- Lambda light chain nephropathy
- Ipp Gelfand syndrome
- Specific immunoglobulin response defect
- Light chain disease
- Predominantly B-cell defect
Frequently Asked Questions
What is the ICD-10 code for other immunodeficiencies with predominantly antibody defects?
The ICD-10-CM code for other immunodeficiencies with predominantly antibody defects is D80.8. The full clinical description is "Other immunodeficiencies with predominantly antibody defects". D80.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D80.8 mean?
ICD-10-CM code D80.8 represents “Other immunodeficiencies with predominantly antibody defects”. 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 D80.8 a billable code?
Yes, D80.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D80.8 in?
D80.8 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D80.8?
D80.8 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 D80.8 map to?
D80.8 maps to 20 SNOMED CT concepts: 127390005, 783205005, 19754005, 449408005, 449409002, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D80.8?
D80.8 is linked to 2 UMLS Concept Unique Identifiers: C3248381, C0477323. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D80.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other immunodeficiencies with predominantly antibody defects 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 D80.8?
D80.8 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.