AutoICD API

D84.89

Billable

Other immunodeficiencies

Other immunodeficiencies

Status

Billable / Specific

Block

D80-D89

Parent Code

D84.8

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(2)
D84.81

Immunodeficiency due to conditions classified elsewhere

BillableD84.82

Immunodeficiency due to drugs and external causes

Also Known As / Clinical Terms(353)

SNOMED CT

UMLS

Clinical Terms

  • T-cell immunodeficiency with epidermodysplasia verruciformis
  • Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency
  • Adult-onset immunodeficiency
  • Immunodeficiency due to natural-killer cell deficiency
  • Interleukin 21 related infantile inflammatory bowel disease
  • Autosomal recessive MSMD (mendelian susceptibility to mycobacterial disease) due to complete RORgamma receptor mutation
  • Deficiency of immunoglobulin secretion
  • Susceptibility to infection due to tyrosine kinase 2 deficiency
  • Constitutional mismatch repair deficiency syndrome due to PMS1 homolog 2, mismatch repair system component mutation
  • Mendelian susceptibility to mycobacterial disease
  • T-cell immunodeficiency due to RHOH deficiency
  • Predisposition to severe viral infection due to IRF7 deficiency
  • Mannose-binding lectin deficiency
  • Mendelian susceptibility to mycobacterial disease due to partial STAT1 (signal transducer and activator of transcription 1) deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency
  • Autoimmune leukopenia
  • Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation
  • Interleukin-2 receptor alpha chain deficiency
  • Neutrophil immunodeficiency syndrome
  • Refractory neutropenia
  • CMMR-D (constitutional mismatch repair deficiency) syndrome
  • FCU - familial cold urticaria
  • Cold-induced angioedema-urticaria
  • Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome
  • Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome
  • Mannose-binding lectin protein deficiency
  • Lymphopenia
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation
  • PASLI - p110-delta-activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency
  • Predisposition to invasive fungal disease due to CARD9 deficiency
  • MSMD - mendelian susceptibility to mycobacterial disease
  • Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome
  • Cell-mediated immune deficiency
  • Congenital immunodeficiency involving the haematopoietic system
  • Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
  • Constitutional mismatch repair deficiency syndrome due to PMS2 mutation
  • Autosomal recessive hyper-IgE (immunoglobulin E) syndrome due to TYK2 deficiency
  • T-cell immunodeficiency due to ras homolog family member H deficiency
  • MBP deficiency
  • Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88
  • EXTL3 (exostosin like glycosyltransferase 3) related neuro-immuno-skeletal dysplasia syndrome
  • CAIN (CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction) syndrome
  • MDA5 deficiency
  • Absent thumb with short stature and immunodeficiency syndrome
  • MBL deficiency
  • Autosomal recessive primary immunodeficiency with defective spontaneous NK (natural killer) cell cytotoxicity
  • Defective phagocytic cell opsonisation
  • MDA5 (melanoma differentiation-associated gene 5) deficiency
  • Schimke syndrome
  • WILD syndrome
  • Susceptibility to infection due to TYK2 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency
  • Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency
  • PLCG2 (phospholipase C gamma 2) associated antibody deficiency and immune dysregulation
  • Secretory piece deficiency
  • Cold urticaria
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency
  • Immunodeficiency due to CD25 deficiency
  • Mendelian susceptibility to mycobacterial infection
  • Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome
  • Schimke immunoosseous dysplasia
  • T-lymphocyte deficiency
  • Warts, immunodeficiency, lymphoedema, anogenital dysplasia syndrome
  • Immunoglobulin-associated molecule deficiency
  • FACU - familial atypical cold urticaria
  • Autoimmune leucopenia
  • CD4 T lymphocyte deficiency
  • Yeast opsonisation defect
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency
  • Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies
  • Activated phosphoinositide 3-kinase delta syndrome
  • MYSM1 deficiency
  • Yeast opsonization defect
  • CD16 deficiency
  • Lymphocytopenia
  • Familial cold autoinflammatory syndrome
  • MBL2 deficiency
  • Immunodeficiency 14
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial JAK1 deficiency
  • Lymphocyte count below reference range
  • Pyogenic bacterial infection due to MyD88 deficiency
  • Early-onset autoimmunity, autoinflammation, immunodeficiency syndrome due to SOCS1 haploinsufficiency
  • Griscelli syndrome with immunodeficiency
  • Immunodeficiency due to ficolin 3 deficiency
  • Invasive candidiasis, deep dermatophytosis syndrome
  • T-lymphocyte immunodeficiency
  • Melanoma differentiation-associated gene 5 deficiency
  • Familial cold urticaria
  • MYSM1 (Myb like, SWIRM and MPN domains 1) deficiency
  • NCKAP1L-associated hyperinflammatory disorder
  • Schimke immuno-osseous dysplasia
  • Griscelli syndrome type 3
  • Hypopigmentation-immunodeficiency disease
  • Mendelian susceptibility to mycobacterial disease due to partial IRF8 (interferon regulatory factor 8) deficiency
  • IL21-related infantile inflammatory bowel disease
  • FADD-related immunodeficiency
  • Immunodeficiency due to mutation of FAS-associated protein with death domain gene
  • Aplasia of thumb
  • Natural-killer cell deficiency
  • Cold-induced angio-oedema-urticaria
  • Secretory component deficiency
  • Autosomal dominant immunodeficiency due to activated p110-delta syndrome
  • Disseminated warts, impaired cell-mediated immunity, primary lymphedema, anogenital dysplasia syndrome
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
  • Mendelian susceptibility to mycobacterial disease due to partial IRF8 deficiency
  • Age-related immunodeficiency
  • Defective phagocytic cell opsonization
  • Mendelian susceptibility to mycobacterial disease due to partial STAT1 deficiency
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
  • Transient immunodeficiency of infancy
  • Alymphocytosis
  • Adult-onset immunodeficiency with acquired anti-interferon-gamma autoantibodies
  • Predisposition to severe viral infection due to interferon regulatory factor 7 deficiency
  • Immunologic defect
  • Immune defect
  • Mannan-binding protein deficiency
  • T-cell immunodeficiency due to RHOH (ras homolog family member H) deficiency
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
  • Griscelli syndrome
  • Autosomal recessive primary immunodeficiency due to RORC mutation
  • Hypopigmentation-immunodeficiency disease type 3
  • PLCG2-associated antibody deficiency and immune dysregulation
  • T lymphocyte disorder
  • CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome
  • Chediak-Higashi-like syndrome
  • Immuno-osseous dysplasia
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial janus kinase 1 deficiency
  • Mendelian susceptibility to mycobacterial disease due to complete ISG15 (interferon stimulated gene 15) deficiency
  • HEM1 deficiency syndrome
  • EXTL3-related neuro-immuno-skeletal dysplasia syndrome
  • Early-onset autoimmunity, autoinflammation, immunodeficiency syndrome due to suppressor of cytokine signaling 1 haploinsufficiency
  • Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RORgamma receptor mutation
  • Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency
  • Heritable disorder of neutrophil function
  • CEBPE-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome
  • Defective immunoglobulin glycosylation
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
  • Cellular immune defect
  • Deficiency of cell mediated immunity
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR1 deficiency
  • Deficiency of cell-mediated immunity
  • Interleukin-12 deficiency
  • Myelodysplastic syndrome with low blasts
  • APDS - activated PI3K-delta syndrome
  • Congenital immunodeficiency involving the hematopoietic system
  • IFIH1 (interferon induced with helicase C domain 1) deficiency
  • Familial hyperinflammatory lymphoproliferative immunodeficiency
  • Griscelli syndrome type 1
  • Mendelian susceptibility to mycobacterial disease due to complete IFNgammaR2 deficiency
  • Partial albinism with immunodeficiency
  • p110-delta-activating mutation causing senescent T cells, lymphadenopathy and immunodeficiency
  • Myelodysplastic neoplasm with low blasts
  • Lichtenstein syndrome
  • Constitutional mismatch repair deficiency syndrome
  • Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial IFNgammaR2 deficiency
  • Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency
  • Immunodeficiency with major anomalies
  • Cryopyrin associated periodic syndrome
  • Activated PI3K-delta syndrome
  • Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 (exostosin like glycosyltransferase 3) deficiency
  • Hypopigmentation-immunodeficiency disease type 1
  • FADD (FAS-associated protein with death domain) related immunodeficiency
  • Phagocytic immunodeficiency
  • WILD (warts, immunodeficiency, lymphoedema, anogenital dysplasia) syndrome
  • Mannose-binding protein deficiency
  • Predominantly T-cell defect
  • Urticaria caused by cold
  • Constitutional mismatch repair deficiency syndrome due to PMS2 deficiency
  • SOCS1-related autoinflammatory syndrome
  • WILD (warts, immunodeficiency, lymphedema, anogenital dysplasia) syndrome
  • Disseminated warts, impaired cell-mediated immunity, primary lymphoedema, anogenital dysplasia syndrome
  • FCAS - familial cold autoinflammatory syndrome
  • Immunodeficiency due to ficolin-3 deficiency
  • Familial cold urticaria with common variable immunodeficiency
  • Neuro-immuno-skeletal dysplasia syndrome due to EXTL3 deficiency
  • Immunodeficiency associated with multiple organ system abnormalities
Frequently Asked Questions
What is the ICD-10 code for other immunodeficiencies?

The ICD-10-CM code for other immunodeficiencies is D84.89. The full clinical description is "Other immunodeficiencies". D84.89 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code D84.89 mean?

ICD-10-CM code D84.89 represents “Other 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 D84.89 a billable code?

Yes, D84.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is D84.89 in?

D84.89 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).

What codes cannot be used with D84.89?

D84.89 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 D84.89 map to?

D84.89 maps to 73 SNOMED CT concepts: 711480000, 719685004, 735536003, 784393004, 234642007, and 68 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for D84.89?

D84.89 is linked to 1 UMLS Concept Unique Identifier: C0494264. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does D84.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other 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 D84.89?

There is no direct ICD-11 mapping available for D84.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.