D83.8
BillableOther common variable immunodeficiencies
Other common variable immunodeficiencies
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
- 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
- Autosomal recessive CVID (common variable immunodeficiency) due to CD81 deficiency1351267003
- Autosomal recessive common variable immunodeficiency due to CD81 deficiency1351267003
- CVID (common variable immunodeficiency) due to TACI deficiency1351268008
- CVID (common variable immunodeficiency) due to TNFRSF13B gene mutation1351268008
- Common variable immunodeficiency due to TACI deficiency1351268008
- Common variable immunodeficiency due to transmembrane activator and calcium-modulator and cyclophilin ligand interactor deficiency1351268008
- X-linked common variable immune deficiency due to CIN85 deficiency1351642008
- X-linked common variable immunodeficiency due to SH3 domain containing kinase binding protein 1 deficiency1351642008
- X-linked common variable immunodeficiency due to SH3KBP1 deficiency1351642008
- Autosomal recessive CVID (common variable immunodeficiency) due to CD20 deficiency1351960005
- Autosomal recessive common variable immunodeficiency due to CD20 deficiency1351960005
- Autosomal recessive common variable immunodeficiency due to CD20 mutation1351960005
- Autosomal recessive common variable immunodeficiency due to MS4A1 mutation1351960005
- Autosomal recessive common variable immunodeficiency due to membrane spanning 4-domains A1 mutation1351960005
- Autosomal recessive CVID (common variable immunodeficiency) due to CD21 deficiency1351961009
- Autosomal recessive common variable immunodeficiency due to CD21 deficiency1351961009
- Autosomal recessive common variable immunodeficiency due to CD21 mutation1351961009
- Autosomal recessive common variable immunodeficiency due to CR2 mutation1351961009
- Autosomal recessive common variable immunodeficiency due to complement C3d receptor 2 mutation1351961009
- Autosomal recessive CVID (combined variable immunodeficiency) due to TNFRSF13C mutation1352023006
- Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation1352023006
- Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency1352023006
- Autosomal recessive combined variable immunodeficiency due to BAFF-R deficiency1352023006
- Autosomal recessive combined variable immunodeficiency due to BAFF-R mutation1352023006
- Autosomal dominant CVID (combined variable immunodeficiency) due to TNFSF12 mutation1352026003
- Autosomal dominant combined variable immunodeficiency due to TWEAK deficiency1352026003
- Autosomal dominant combined variable immunodeficiency due to TWEAK mutation1352026003
- Autosomal dominant combined variable immunodeficiency due to tumor necrosis factor-like weak inducer of apoptosis mutation1352026003
- Autosomal dominant combined variable immunodeficiency due to tumour necrosis factor-like weak inducer of apoptosis mutation1352026003
- Autosomal dominant CVID (combined variable immunodeficiency) due to NFKB1 deficiency1354416002
- Autosomal dominant combined variable immunodeficiency due to NFKB1 deficiency1354416002
- Autosomal dominant combined variable immunodeficiency due to NFKB1 mutation1354416002
- Autosomal dominant combined variable immunodeficiency due to nuclear factor kappa B subunit 1 mutation1354416002
- Autosomal dominant CVID (combined variable immunodeficiency) due to IRF2BP2 deficiency1354420003
- Autosomal dominant combined variable immunodeficiency due to IRF2BP2 deficiency1354420003
- Autosomal dominant combined variable immunodeficiency due to IRF2BP2 mutation1354420003
- Autosomal dominant combined variable immunodeficiency due to interferon regulatory factor 2 binding protein 2 mutation1354420003
- Autosomal recessive CVID (combined variable immunodeficiency) due to ARHGEF1 deficiency1354472008
- Autosomal recessive combined variable immunodeficiency due to ARHGEF1 deficiency1354472008
- Autosomal recessive combined variable immunodeficiency due to ARHGEF1 mutation1354472008
- Autosomal recessive combined variable immunodeficiency due to Rho guanine nucleotide exchange factor 1 mutation1354472008
- Autosomal dominant CVID (combined variable immunodeficiency) due to SEC61A1 deficiency1354480001
- Autosomal dominant combined variable immunodeficiency due to SEC61 translocon subunit alpha 1 mutation1354480001
- Autosomal dominant combined variable immunodeficiency due to SEC61A1 deficiency1354480001
- Autosomal dominant combined variable immunodeficiency due to SEC61A1 mutation1354480001
- Autosomal recessive CVID (combined variable immunodeficiency) due to PIK3CG deficiency1354483004
- Autosomal recessive combined variable immunodeficiency due to PIK3CG deficiency1354483004
- Autosomal recessive combined variable immunodeficiency due to PIK3CG mutation1354483004
- Autosomal recessive combined variable immunodeficiency due to phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma mutation1354483004
- Autosomal recessive common variable immunodeficiency due to BOB1 deficiency1354596000
- Autosomal recessive common variable immunodeficiency due to POU class 2 homeobox associating factor 1 mutation1354596000
- Autosomal recessive common variable immunodeficiency due to POU2AF1 mutation1354596000
- Autosomal recessive CVID (common variable immunodeficiency) due to RAC2 mutation1356782005
- Autosomal recessive common variable immunodeficiency due to RAC2 deficiency1356782005
- Autosomal recessive common variable immunodeficiency due to RAC2 mutation1356782005
- Autosomal recessive common variable immunodeficiency due to Rac family small GTPase 2 deficiency1356782005
Frequently Asked Questions
What is ICD-10 code D83.8?
ICD-10-CM code D83.8 represents "Other common variable immunodeficiencies". It is a billable/specific code that can be used on a claim.
Is D83.8 a billable code?
Yes, D83.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D83.8 in?
D83.8 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D83.8?
D83.8 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 D83.8 map to?
D83.8 maps to 14 SNOMED CT concepts: 1354420003, 1354416002, 1354480001, 1352026003, 1354472008, and 9 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D83.8?
D83.8 is linked to 1 UMLS Concept Unique Identifier: C0477327. 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.