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) 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)
- transplant failure and rejection (T86.-)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code D89.0?
ICD-10-CM code D89.0 represents "Polyclonal hypergammaglobulinemia". It 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.
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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.