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ICD-10-CM Codes
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D50-D89
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Certain disorders involving the immune mechanism D80-D89
Certain disorders involving the immune mechanism D80-D89
Type 1 ExcludesType 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 D80-D89. 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.
- autoimmune disease (systemic) NOS (
ICD-10-CM Diagnosis Code M35.9
Systemic involvement of connective tissue, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Autoimmune disease (systemic) NOS
- Collagen (vascular) disease NOS
M35.9) - functional disorders of polymorphonuclear neutrophils (
ICD-10-CM Diagnosis Code D71
Functional disorders of polymorphonuclear neutrophils
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Cell membrane receptor complex [CR3] defect
- Chronic (childhood) granulomatous disease
- Congenital dysphagocytosis
- Progressive septic granulomatosis
D71) - human immunodeficiency virus [HIV] disease (
ICD-10-CM Diagnosis Code B20
Human immunodeficiency virus [HIV] disease
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Code First- Human immunodeficiency virus [HIV] disease complicating pregnancy, childbirth and the puerperium, if applicable (O98.7-)
Includes- acquired immune deficiency syndrome [AIDS]
- AIDS-related complex [ARC]
- HIV infection, symptomatic
Type 1 Excludes- asymptomatic human immunodeficiency virus [HIV] infection status (Z21)
- exposure to HIV virus (Z20.6)
- inconclusive serologic evidence of HIV (R75)
Use Additional- code(s) to identify all manifestations of HIV infection
B20)
IncludesIncludes Help
"Includes" further defines, or give examples of, the content of the code or category.
- defects in the complement system
- immunodeficiency disorders, except human immunodeficiency virus [HIV] disease
- sarcoidosis
Codes
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D80 Immunodeficiency with predominantly antibody defects
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D81 Combined immunodeficiencies
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D82 Immunodeficiency associated with other major defects
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D83 Common variable immunodeficiency
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D84 Other immunodeficiencies
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D86 Sarcoidosis
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D89 Other disorders involving the immune mechanism, not elsewhere classified
ICD-10-CM Diagnosis Codes D80-*
- D80 Immunodeficiency with predominantly antibody ...
- D80.0 Hereditary hypogammaglobulinemia
- D80.1 Nonfamilial hypogammaglobulinemia
- D80.2 Selective deficiency of immunoglobulin A [IgA...
- D80.3 Selective deficiency of immunoglobulin G [IgG...
- D80.4 Selective deficiency of immunoglobulin M [IgM...
- D80.5 Immunodeficiency with increased immunoglobuli...
- D80.6 Antibody deficiency with near-normal immunogl...
- D80.7 Transient hypogammaglobulinemia of infancy
- D80.8 Other immunodeficiencies with predominantly a...
- D80.9 Immunodeficiency with predominantly antibody ...
ICD-10-CM Diagnosis Codes D81-*
- D81 Combined immunodeficiencies
- D81.0 Severe combined immunodeficiency [SCID] with ...
- D81.1 Severe combined immunodeficiency [SCID] with ...
- D81.2 Severe combined immunodeficiency [SCID] with ...
- D81.3 Adenosine deaminase [ADA] deficiency
- D81.30 Adenosine deaminase deficiency, unspecified
- D81.31 Severe combined immunodeficiency due to adeno...
- D81.32 Adenosine deaminase 2 deficiency
- D81.39 Other adenosine deaminase deficiency
- D81.4 Nezelof's syndrome
- D81.5 Purine nucleoside phosphorylase [PNP] deficie...
- D81.6 Major histocompatibility complex class I defi...
- D81.7 Major histocompatibility complex class II def...
- D81.8 Other combined immunodeficiencies
- D81.81 Biotin-dependent carboxylase deficiency
- D81.810 Biotinidase deficiency
- D81.818 Other biotin-dependent carboxylase deficiency...
- D81.819 Biotin-dependent carboxylase deficiency, unsp...
- D81.82 Activated Phosphoinositide 3-kinase Delta Syn...
- D81.89 Other combined immunodeficiencies
- D81.9 Combined immunodeficiency, unspecified
ICD-10-CM Diagnosis Codes D82-*
- D82 Immunodeficiency associated with other major ...
- D82.0 Wiskott-Aldrich syndrome
- D82.1 Di George's syndrome
- D82.2 Immunodeficiency with short-limbed stature
- D82.3 Immunodeficiency following hereditary defecti...
- D82.4 Hyperimmunoglobulin E [IgE] syndrome
- D82.8 Immunodeficiency associated with other specif...
- D82.9 Immunodeficiency associated with major defect...
ICD-10-CM Diagnosis Codes D83-*
- D83 Common variable immunodeficiency
- D83.0 Common variable immunodeficiency with predomi...
- D83.1 Common variable immunodeficiency with predomi...
- D83.2 Common variable immunodeficiency with autoant...
- D83.8 Other common variable immunodeficiencies
- D83.9 Common variable immunodeficiency, unspecified...
ICD-10-CM Diagnosis Codes D84-*
- D84 Other immunodeficiencies
- D84.0 Lymphocyte function antigen-1 [LFA-1] defect
- D84.1 Defects in the complement system
- D84.8 Other specified immunodeficiencies
- D84.81 Immunodeficiency due to conditions classified...
- D84.82 Immunodeficiency due to drugs and external ca...
- D84.821 Immunodeficiency due to drugs
- D84.822 Immunodeficiency due to external causes
- D84.89 Other immunodeficiencies
- D84.9 Immunodeficiency, unspecified
ICD-10-CM Diagnosis Codes D86-*
- D86 Sarcoidosis
- D86.0 Sarcoidosis of lung
- D86.1 Sarcoidosis of lymph nodes
- D86.2 Sarcoidosis of lung with sarcoidosis of lymph...
- D86.3 Sarcoidosis of skin
- D86.8 Sarcoidosis of other sites
- D86.81 Sarcoid meningitis
- D86.82 Multiple cranial nerve palsies in sarcoidosis...
- D86.83 Sarcoid iridocyclitis
- D86.84 Sarcoid pyelonephritis
- D86.85 Sarcoid myocarditis
- D86.86 Sarcoid arthropathy
- D86.87 Sarcoid myositis
- D86.89 Sarcoidosis of other sites
- D86.9 Sarcoidosis, unspecified
ICD-10-CM Diagnosis Codes D89-*
- D89 Other disorders involving the immune mechanis...
- D89.0 Polyclonal hypergammaglobulinemia
- D89.1 Cryoglobulinemia
- D89.2 Hypergammaglobulinemia, unspecified
- D89.3 Immune reconstitution syndrome
- D89.4 Mast cell activation syndrome and related dis...
- D89.40 Mast cell activation, unspecified
- D89.41 Monoclonal mast cell activation syndrome
- D89.42 Idiopathic mast cell activation syndrome
- D89.43 Secondary mast cell activation
- D89.44 Hereditary alpha tryptasemia
- D89.49 Other mast cell activation disorder
- D89.8 Other specified disorders involving the immun...
- D89.81 Graft-versus-host disease
- D89.810 Acute graft-versus-host disease
- D89.811 Chronic graft-versus-host disease
- D89.812 Acute on chronic graft-versus-host disease
- D89.813 …… unspecified
- D89.82 Autoimmune lymphoproliferative syndrome [ALPS...
- D89.83 Cytokine release syndrome
- D89.89 Other specified disorders involving the immun...
- D89.9 Disorder involving the immune mechanism, unsp...
| D50-D89
ICD-10-CM Range D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism- D50-D53 Nutritional anemias
- D55-D59 Hemolytic anemias
- D60-D64 Aplastic and other anemias and other bon...
- D65-D69 Coagulation defects, purpura and other h...
- D70-D77 Other disorders of blood and blood-formi...
- D78-D78 Intraoperative and postprocedural compli...
- D80-D89 Certain disorders involving the immune m...
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D78-D78 ICD-10-CM Range D78-D78 Intraoperative and postprocedural complications of the spleen- D78 Intraoperative and postprocedural compli...
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| E00-E89
ICD-10-CM Range E00-E89 Endocrine, nutritional and metabolic diseases- E00-E07 Disorders of thyroid gland
- E08-E13 Diabetes mellitus
- E15-E16 Other disorders of glucose regulation an...
- E20-E35 Disorders of other endocrine glands
- E36-E36 Intraoperative complications of endocrin...
- E40-E46 Malnutrition
- E50-E64 Other nutritional deficiencies
- E65-E68 Overweight, obesity and other hyperalime...
- E70-E88 Metabolic disorders
- E89-E89 Postprocedural endocrine and metabolic c...
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