2014 ICD-9-CM Diagnosis Code 279.8
Other specified disorders involving the immune mechanism
- 2014
- Billable Thru Sept 30/2015
- Non-Billable On/After Oct 1/2015
- Short description: Immune mechanism dis NEC.
- ICD-9-CM 279.8 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 279.8 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2014 version of ICD-9-CM 279.8.
- More recent version(s) of ICD-9-CM 279.8: 2015.
Convert to ICD-10-CM:
279.8 converts approximately to:
- 2015/16 ICD-10-CM D84.1 Defects in the complement system
Or:
- 2015/16 ICD-10-CM D89.89 Other specified disorders involving the immune mechanism, not elsewhere classified
Or:
- 2015/16 ICD-10-CM M35.9 Systemic involvement of connective tissue, unspecified
Approximate Synonyms
- Abnormal host defense
- Adult linear immunoglobulin A disease
- Age-related immunodeficiency
- Alternative pathway deficiency
- Anaphylotoxin inactivator deficiency
- Angioedema due to disorder of C1 esterase inhibitor
- Autoimmune AND/OR graft reaction
- Autologous state
- Classical complement pathway abnormality
- Clonal anergy
- Complement 1q beta chain deficiency
- Complement 1q deficiency
- Complement 1q dysfunction
- Complement 1r deficiency
- Complement 1s deficiency
- Complement 2 deficiency
- Complement 3 deficiency
- Complement 4 binding protein deficiency
- Complement 4 deficiency
- Complement 4A deficiency
- Complement 4B deficiency
- Complement 5 deficiency
- Complement 5 dysfunction
- Complement 5a inhibitor deficiency
- Complement 6 deficiency
- Complement 7 deficiency
- Complement 8 alpha-gamma deficiency
- Complement 8 beta chain deficiency
- Complement 8 beta chain dysfunction
- Complement 9 deficiency
- Complement abnormality
- Complement component deficiency
- Complement deficiency C4
- Complement deficiency disease
- Complement level below reference range (disorder)
- Complement receptor 1 deficiency
- Complement receptor 3 deficiency
- Complement receptor deficiency
- Complement regulatory factor defect
- Cutis laxa with complement deficiency
- Decay accelerating factor deficiency
- Defective phagocytic cell chemotaxis
- Disorder of complement
- Factor B deficiency
- Factor D deficiency
- Factor H deficiency
- Familial C3B inhibitor deficiency syndrome
- Familial immunoglobulin hypercatabolism
- Hereditary C1 esterase inhibitor deficiency - deficient factor
- Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
- Homologous restriction factor deficiency
- Hyperimmune state
- Hyperimmunoglobulin D with periodic fever
- Hypocomplementemia
- Immune reconstitution syndrome
- Immunodeficiency associated with chromosomal abnormality
- Immunodeficiency due to major defect
- Immunodeficiency following hereditary defective response to epstein-barr virus
- Immunodeficiency with major anomalies
- Immunodeficiency, respon to epstein-barr virus
- Immunoglobulin hypercatabolism
- Kappa light chain disease
- Lymphocyte function antigen-1 defect
- Neutrophil secondary granule deficiency
- Panniculitis with complement deficiency
- Phagocytic cell defect
- Postinfectious autoimmune reaction
- Predominant humoral immune deficiency
- Primary immune deficiency disorder
- Primary immunoglobulin catabolism abnormality
- Properdin deficiency disease
- Reticuloendothelial blockade
- Secondary immune deficiency disorder
- Terminal component deficiency
- T-lymphocyte deficiency
- X-linked hyperimmunoglobulin M syndrome
Applies To
- Single complement [C1-C9] deficiency or dysfunction
complement factor NEC 279.8
immune mechanism (immunity) 279.9
