279.8 - Other Specified Disorders Involving The Immune Mechanism
The ICD 9 Code for Other specified disorders involving the immune mechanism is listed as 279.8.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
| ICD 9 CM Field | Value |
|---|---|
| Diagnosis Code: | 279.8 |
| Long Description: | Other specified disorders involving the immune mechanism |
| Short Description: | Immune mechanism dis NEC |
| Chapter: | Endocrine, Nutritional And Metabolic Diseases, And Immunity Disorders |
| Block: | Other Metabolic Disorders And Immunity Disorders (270-279) |
| Related Descriptions: |
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 T-lymphocyte deficiency Terminal component deficiency X-linked hyperimmunoglobulin M syndrome |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | D84.1 - Defects in the complement system (approximate) |
| ICD-10-CM Code: | D89.89 - Other specified disorders involving the immune mechanism, not elsewhere classified (approximate) |
| ICD-10-CM Code: | M35.9 - Systemic involvement of connective tissue, unspecified (approximate) |
| ICD-9-CM Siblings (same level / similar specificity) of 279.8: | |
| 279.2 - Combined immunity deficiency | |
| 279.3 - Unspecified immunity deficiency | |
| 279.9 - Unspecified disorder of immune mechanism | |