Diagnosis Code: 279.8

Short Description: Immune mechanism dis NEC

Long Description: Other specified disorders involving the immune mechanism

Code Classification:

• Endocrine, nutritional and metabolic diseases, and immunity disorders (240–279)
  • Other metabolic disorders and immunity disorders (270-279)
    • 279 Disorders involving the immune mechanism
      • 279.8 Immune mechanism dis NEC

Code Version: 2015 ICD-9-CM

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 disease
• 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
• Disorder of kidney due to kappa light chain disease
• Disorder of kidney due to lambda light chain disease
• 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
• Immune reconstitution syndrome
• Immunodeficiency associated with chromosomal abnormality
• Immunodeficiency with major anomalies
• Immunoglobulin hypercatabolism
• Kappa light chain disease
• 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

References to Index of Diseases and Injuries

The code 279.8 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Deficiency, deficient
  • complement factor NEC 279.8

• Depletion
  • complement factor 279.8

• Disorder - see also Disease
  • immune mechanism (immunity) 279.9
    • single complement (C1-C9)�279.8
    • specified type NEC 279.8
  • single complement (C1-C9)�279.8

• Hypocomplementemia 279.8

Crosswalk Information

The code 279.8 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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