D89.0  Polyclonal hypergammaglobulinemia
ICD-10-CM Code Details and Notes
D89.0 is a billable medical code.

Inclusion Term(s)
   • Benign hypergammaglobulinemic purpura
   • Polyclonal gammopathy NOS

- ICD-10-CM Chapters, Sections & Parents

D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Excludes 2:
   • 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)

D80-D89 Certain disorders involving the immune mechanism

   • defects in the complement system
   • immunodeficiency disorders, except human immunodeficiency virus [HIV] disease
   • sarcoidosis

   • autoimmune disease (systemic) NOS (M35.9)
   • functional disorders of polymorphonuclear neutrophils (D71)
   • human immunodeficiency virus [HIV] disease (B20)

D89 Other disorders involving the immune mechanism, not elsewhere classified

   • hyperglobulinemia NOS (R77.1)
   • monoclonal gammopathy (of undetermined significance) (D47.2)

Excludes 2:
   • transplant failure and rejection (T86.-)

ICD-10-CM Index References
• Gammopathy polyclonal
• Hypergammaglobulinemia polyclonal
• Hypergammaglobulinemia Waldenstr?m
• Purpura hypergammaglobulinemic
• Waldenstr?m hypergammaglobulinemia