Diagnosis Code: D84.89

Short Description: Other immunodeficiencies

Long Description: Other immunodeficiencies

The code D84.89 is VALID for claim submission

Code Classification:

• Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50–D89)
  • Certain disorders involving the immune mechanism (D80-D89)
    • Other immunodeficiencies (D84)
      • D84.89 Other immunodeficiencies

Code Version: 2022 ICD-10-CM

Synonyms

• Absent thumb with short stature and immunodeficiency syndrome
• Activated PI3K-delta syndrome
• Adult-onset immunodeficiency
• Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies
• Age-related immunodeficiency
• Autoimmune leukopenia
• Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
• Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
• Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation
• Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
• Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
• Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
• CD4 T lymphocyte deficiency
• CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome
• Cellular immune defect
• Congenital absence of thumb
• Congenital immunodeficiency involving the hematopoietic system
• Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome
• Constitutional mismatch repair deficiency syndrome
• Cryopyrin associated periodic syndrome
• Defective immunoglobulin glycosylation
• Defective phagocytic cell opsonization
• FADD-related immunodeficiency
• Familial cold urticaria
• Griscelli syndrome type 1
• Griscelli syndrome type 3
• Heritable disorder of neutrophil function
• Hypopigmentation-immunodeficiency disease
• Hypopigmentation-immunodeficiency disease
• IL21-related infantile inflammatory bowel disease
• Immune defect
• Immune defect
• Immune defect
• Immune defect
• Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome
• Immunodeficiency associated with multiple organ system abnormalities
• Immunodeficiency associated with multiple organ system abnormalities
• Immunodeficiency due to CD25 deficiency
• Immunodeficiency due to ficolin 3 deficiency
• Immunodeficiency with major anomalies
• Immunodeficiency with major anomalies
• Immunoglobulin-associated molecule deficiency
• Immuno-osseous dysplasia
• Immuno-osseous dysplasia
• Immuno-osseous dysplasia
• Interleukin-12 deficiency
• Lichtenstein syndrome
• Lymphocyte count below reference range
• Lymphocytopenia
• Mannan-binding protein deficiency
• Mannose-binding lectin deficiency
• MDA5 deficiency
• Mendelian susceptibility to mycobacterial disease
• Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency
• Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency
• Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
• Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency
• Natural-killer cell deficiency
• Neutrophil immunodeficiency syndrome
• Phagocytic immunodeficiency
• PLCG2-associated antibody deficiency and immune dysregulation
• Predisposition to invasive fungal disease due to CARD9 deficiency
• Predominantly T-cell defect
• Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
• Schimke immuno-osseous dysplasia
• Secretory piece deficiency
• Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome
• Susceptibility to infection due to TYK2 deficiency
• T lymphocyte disorder
• T-cell immunodeficiency with epidermodysplasia verruciformis
• T-lymphocyte deficiency
• T-lymphocyte immunodeficiency
• Transient immunodeficiency of infancy
• Urticaria due to cold
• Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome

Diagnostic Related Group(s)

The code D84.89 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Reticuloendothelial And Immunity Disorders With Mcc (814)
• Reticuloendothelial And Immunity Disorders With Cc (815)
• Reticuloendothelial And Immunity Disorders Without Cc/mcc (816)

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This page was last updated on: 10/1/2023

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