D84.9
BillableImmunodeficiency, unspecified
Immunodeficiency, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Immunocompromised NOS
- Immunodeficient NOS
- Immunosuppressed NOS
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) NOS (M35.9)
- certain conditions originating in the perinatal period (P00-P96)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- human immunodeficiency virus [HIV] disease (B20)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- Good syndrome9893005
- Good's syndrome9893005
- Immunodeficiency with thymoma9893005
- Secondary immune deficiency disorder33286000
- Secondary immunodeficiency33286000
- Congenital immunodeficiency disease36138009
- Immunosuppression38013005
- Disseminated dermatophytosis40911008
- Primary immune deficiency disorder58606001
- Primary immunodeficiency58606001
- Ovarian dysgenesis with normal chromosomes95198001
- Pure gonadal dysgenesis 46,XX95198001
- Pure gonadal dysgenesis95219002
- Immunodeficiency secondary to neoplasm103077004
- Immunodeficiency secondary to trauma103078009
- Immunodeficiency caused by corticosteroid103079001
- Immunodeficiency secondary to corticosteroid103079001
- Immunodeficiency secondary to chemotherapy103081004
- Ovarian dysgenesis205683001
- Immunodeficiency234532001
- Immunodeficiency disease234532001
- Immunodeficiency disorder234532001
- Complement component 3 inactivator deficiency234621005
- Complement factor 3i deficiency234621005
- Factor I deficiency234621005
- Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency234633000
- Centromeric instability, immunodeficiency syndrome234633000
- Immunodeficiency-centromeric instability-facial anomalies syndrome234633000
- Microcephaly, normal intelligence and immunodeficiency234638009
- NBS - Nijmegen breakage syndrome234638009
- Nijmegen breakage syndrome234638009
- Seemanova syndrome II234638009
- Age-related immunodeficiency234642007
- Drug-induced immunodeficiency234645009
- Livedo racemosa238772004
- Livedo reticularis238772004
- Immuno-osseous dysplasia254067002
- CMTC - Cutis marmorata telangiectatica congenita254778000
- Congenital livedo reticularis254778000
- Cutis marmorata telangiectasia congenita254778000
- Cutis marmorata telangiectatica congenita254778000
- Van Lohuizen's syndrome254778000
- Patient immunocompromised370388006
- Patient immunosuppressed370391006
- Congenital anomaly of endocrine ovary370966000
- Oral hairy leucoplakia associated with immunodeficiency402900005
- Oral hairy leukoplakia associated with immunodeficiency402900005
- Anhidrotic ectodermal dysplasia with immune deficiency703525006
- Anhidrotic ectodermal dysplasia with immunodeficiency703525006
- Hypohidrotic ectodermal dysplasia with immune deficiency703525006
- Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome721977007
- Laron syndrome with immunodeficiency724179008
- Laron-like syndrome724179008
- Short stature due to STAT5b (signal transducer and activator of transcription 5b) deficiency724179008
- Adult-onset immunodeficiency735536003
- FILS (facial dysmorphism, immunodeficiency, livedo, short stature) syndrome771515001
- FILS syndrome771515001
- Facial dysmorphism, immunodeficiency, livedo, short stature syndrome771515001
- Roifman syndrome773404000
- Spondyloepiphyseal dysplasia, retinal dystrophy, immunodeficiency syndrome773404000
- STAT1 deficiency778045003
- Signal transducer and activator of transcription 1 deficiency778045003
- Susceptibility to viral and mycobacterial infection778045003
- Iatrogenic immunodeficiency-associated lymphoproliferative disorder783150002
- Primary immunodeficiency with post-MMR (measles-mumps-rubella) vaccine viral infection783245001
- Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection783245001
- Complete factor I deficiency783621008
- Immunodeficiency with factor I anomaly783621008
- Disseminated dermatophytosis due to immunodeficiency840435003
- Immunodeficiency disseminated dermatophytosis840435003
- Adenovirus infection in immunocompromised person1264007008
- Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA GOF (gain of function) mutation1354646005
- Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation1354646005
- Anhidrotic ectodermal dysplasia with immune deficiency due to NFKBIA gain of function mutation1354646005
- Anhidrotic ectodermal dysplasia with immune deficiency due to nuclear factor kappa-B inhibitor alpha, gain of function mutation1354646005
- Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB GOF mutation1366698006
- Anhidrotic ectodermal dysplasia with immune deficiency due to IKBKB gain of function mutation1366698006
- Immunodeficiency caused by long term therapeutic use of drug10838971000119103
UMLS
- DEFIC SYNDROME IMMUNOLC0021051
- DEFIC SYNDROMES IMMUNOLC0021051
- Decreased immune functionC0021051
- Deficiency Syndrome, ImmunologicC0021051
- Deficiency Syndrome, ImmunologicalC0021051
- Deficiency Syndromes, ImmunologicC0021051
- Deficiency Syndromes, ImmunologicalC0021051
- IMMUNOL DEFIC SYNDROMEC0021051
- IMMUNOL DEFIC SYNDROMESC0021051
- Immune deficiencyC0021051
- ImmunodeficiencyC0021051
- Immunodeficiency DisorderC0021051
- Immunodeficiency NOSC0021051
- Immunodeficiency SyndromeC0021051
- Immunodeficiency diseaseC0021051
- Immunodeficiency disorderC0021051
- Immunodeficiency disorder (disorder)C0021051
- Immunodeficiency syndromesC0021051
- Immunodeficiency, unspecifiedC0021051
- ImmunodeficientC0021051
- Immunodeficient NOSC0021051
- Immunologic Deficiency SyndromeC0021051
- Immunologic Deficiency SyndromesC0021051
- Immunological Deficiency SyndromeC0021051
- Immunological Deficiency SyndromesC0021051
- Syndrome, Immunologic DeficiencyC0021051
- Syndrome, Immunological DeficiencyC0021051
- Syndromes, Immunologic DeficiencyC0021051
- Syndromes, Immunological DeficiencyC0021051
- Unspecified immunity deficiencyC0021051
- hypoimmunityC0021051
- immune deficiencyC0021051
- immune deficiency disorderC0021051
- immunodeficienciesC0021051
- immunodeficiencyC0021051
- immunodeficiency diseaseC0021051
- immunodeficiency disorderC0021051
- immunodeficiency syndromeC0021051
- immunodeficiency syndromesC0021051
- Host, ImmunocompromisedC0085393
- Host, ImmunosuppressedC0085393
- Hosts, ImmunocompromisedC0085393
- Hosts, ImmunosuppressedC0085393
- ImmunocompromisedC0085393
- Immunocompromised HostC0085393
- Immunocompromised HostsC0085393
- Immunocompromised NOSC0085393
- Immunocompromised PatientC0085393
- Immunocompromised PatientsC0085393
- ImmunosuppressedC0085393
- Immunosuppressed HostC0085393
- Immunosuppressed HostsC0085393
- Immunosuppressed NOSC0085393
- Immunosuppressed PatientC0085393
- Patient immunocompromisedC0085393
- Patient immunocompromised (finding)C0085393
- Patient immunosuppressedC0085393
- Patient immunosuppressed (finding)C0085393
- Patient, ImmunocompromisedC0085393
- Patients, ImmunocompromisedC0085393
- host immunocompromisedC0085393
- immunocompromisedC0085393
- immunocompromised hostC0085393
- immunocompromised patientC0085393
- immunocompromised patientsC0085393
- immunocompromisingC0085393
- immunosuppressed patientC0085393
- immunosuppressed patientsC0085393
Frequently Asked Questions
What is the ICD-10 code for immunodeficiency, unspecified?
The ICD-10-CM code for immunodeficiency, unspecified is D84.9. The full clinical description is "Immunodeficiency, unspecified". D84.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D84.9 mean?
ICD-10-CM code D84.9 represents "Immunodeficiency, unspecified". 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 D84.9 a billable code?
Yes, D84.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D84.9 in?
D84.9 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D84.9?
D84.9 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 D84.9 map to?
D84.9 maps to 41 SNOMED CT concepts: 1264007008, 735536003, 234642007, 703525006, 1354646005, and 36 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D84.9?
D84.9 is linked to 2 UMLS Concept Unique Identifiers: C0021051, C0085393. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.