D89.0
BillablePolyclonal hypergammaglobulinemia
Polyclonal hypergammaglobulinemia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Benign hypergammaglobulinemic purpura
- Polyclonal gammopathy NOS
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) NOSM35.9
- •certain conditions originating in the perinatal periodP00-P96
- •complications of pregnancy, childbirth and the puerperiumO9A)O00
- •congenital malformations, deformations and chromosomal abnormalitiesQ00-Q99
- •endocrine, nutritional and metabolic diseasesE00-E88
- •human immunodeficiency virus [HIV] diseaseB20
- •injury, poisoning and certain other consequences of external causesS00-T88
- •neoplasmsC00-D49
- •symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classifiedR00-R94
- •transplant failure and rejectionT86
Related Codes(6)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(32)
SNOMED CT
- Polyclonal gammopathy16618004
- Polyclonal hypergammaglobulinaemia190808009
- Polyclonal hypergammaglobulinemia190808009
- Waldenstrom hypergammaglobulinemic purpura190809001
- Waldenstrom's hypergammaglobulinaemic purpura190809001
- Waldenstrom's hypergammaglobulinemic purpura190809001
- Benign primary hypergammaglobulinaemic purpura190810006
- Benign primary hypergammaglobulinemic purpura190810006
- Hyperglobulinemic purpura402852007
UMLS
- Benign hypergammaglobulinemic purpuraC2873855
- Polyclonal HypergammaglobulinemiaC0154254
- Polyclonal hypergammaglobulinaemiaC0154254
- Polyclonal hypergammaglobulinemiaC0154254
- Polyclonal hypergammaglobulinemia (disorder)C0154254
- Polyclonal gammopathyC0272249
- Polyclonal gammopathy (disorder)C0272249
- Polyclonal gammopathy NOSC0272249
- gammopathy polyclonalC0272249
- polyclonal gammopathyC0272249
Clinical Terms
- Waldenstrom's hypergammaglobulinaemic purpura
- Waldenstrom's hypergammaglobulinemic purpura
- Polyclonal gammopathy
- Polyclonal gammopathy (disorder)
- gammopathy polyclonal
- Benign primary hypergammaglobulinaemic purpura
- Polyclonal hypergammaglobulinaemia
- Polyclonal gammopathy NOS
- Hyperglobulinemic purpura
- Polyclonal hypergammaglobulinemia (disorder)
- Waldenstrom hypergammaglobulinemic purpura
- Benign primary hypergammaglobulinemic purpura
- Benign hypergammaglobulinemic purpura
Frequently Asked Questions
What is the ICD-10 code for polyclonal hypergammaglobulinemia?
The ICD-10-CM code for polyclonal hypergammaglobulinemia is D89.0. The full clinical description is "Polyclonal hypergammaglobulinemia". D89.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D89.0 mean?
ICD-10-CM code D89.0 represents “Polyclonal hypergammaglobulinemia”. It is classified under Chapter 3: Diseases of the Blood and Blood-Forming Organs and is a billable/specific code that can be used on a claim.
Is D89.0 a billable code?
Yes, D89.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D89.0 in?
D89.0 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D89.0?
D89.0 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); and 2 more.
What SNOMED CT codes does D89.0 map to?
D89.0 maps to 5 SNOMED CT concepts: 190810006, 402852007, 16618004, 190808009, 190809001. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D89.0?
D89.0 is linked to 3 UMLS Concept Unique Identifiers: C2873855, C0154254, C0272249. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D89.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like polyclonal hypergammaglobulinemia affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of D89.0?
D89.0 maps to the ICD-11 code: 4B21 (Polyclonal hypergammaglobulinaemia).
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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.