D89.2
BillableHypergammaglobulinemia, unspecified
Hypergammaglobulinemia, unspecified
Coding Notes
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(58)
SNOMED CT
- Cryofibrinogenaemia10934005
- Cryofibrinogenemia10934005
- Sneddon-Wilkinson disease25147002
- Sneddon-Wilkinson syndrome25147002
- Subcorneal pustular dermatosis25147002
- Congenital hypergammaglobulinaemia58034007
- Congenital hypergammaglobulinemia58034007
- Asymptomatic monoclonal gammopathy58648008
- Benign monoclonal gammopathy58648008
- Primary cryofibrinogenaemia61802005
- Primary cryofibrinogenemia61802005
- Mixed cryofibrinogenaemia80988005
- Mixed cryofibrinogenemia80988005
- Increased serum protein level81647003
- Serum protein above reference range81647003
- Serum protein level above reference range81647003
- Hypergammaglobulinaemia127388009
- Hypergammaglobulinemia127388009
- Hereditary hypertrophic neuropathy with paraproteinaemia230559003
- Hereditary hypertrophic neuropathy with paraproteinemia230559003
- MGUS - monoclonal gammopathy of uncertain significance277577000
- Monoclonal gammopathy of uncertain significance277577000
- Monoclonal gammopathy of undetermined significance277577000
- Benign paraproteinaemia395692003
- Benign paraproteinemia395692003
- Sneddon-Wilkinson disease with paraproteinaemia403217003
- Sneddon-Wilkinson disease with paraproteinemia403217003
- Subcorneal pustular dermatosis with paraproteinaemia403217003
- Subcorneal pustular dermatosis with paraproteinemia403217003
Clinical Terms
- Congenital hypergammaglobulinemia
- Sneddon-Wilkinson disease with paraproteinaemia
- Subcorneal pustular dermatosis with paraproteinaemia
- Primary cryofibrinogenemia
- Subcorneal pustular dermatosis with paraproteinemia
- Benign monoclonal gammopathy
- Hereditary hypertrophic neuropathy with paraproteinaemia
- Hereditary hypertrophic neuropathy with paraproteinemia
- Hypergammaglobulinaemia
- Congenital hypergammaglobulinaemia
- Sneddon-Wilkinson syndrome
- Benign paraproteinaemia
- MGUS - monoclonal gammopathy of uncertain significance
- Cryofibrinogenemia
- Sneddon-Wilkinson disease
- Serum protein level above reference range
- Monoclonal gammopathy of undetermined significance
- Serum protein above reference range
- Cryofibrinogenaemia
- Benign paraproteinemia
- Sneddon-Wilkinson disease with paraproteinemia
- Mixed cryofibrinogenemia
- Increased serum protein level
- Monoclonal gammopathy of uncertain significance
- Subcorneal pustular dermatosis
- Mixed cryofibrinogenaemia
- Primary cryofibrinogenaemia
- Asymptomatic monoclonal gammopathy
Frequently Asked Questions
What is the ICD-10 code for hypergammaglobulinemia, unspecified?
The ICD-10-CM code for hypergammaglobulinemia, unspecified is D89.2. The full clinical description is "Hypergammaglobulinemia, unspecified". D89.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code D89.2 mean?
ICD-10-CM code D89.2 represents “Hypergammaglobulinemia, unspecified”. 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 D89.2 a billable code?
Yes, D89.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is D89.2 in?
D89.2 is in Chapter 3: Diseases of the Blood and Blood-Forming Organs (codes D50-D89).
What codes cannot be used with D89.2?
D89.2 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 D89.2 map to?
D89.2 maps to 12 SNOMED CT concepts: 58648008, 395692003, 58034007, 10934005, 230559003, and 7 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for D89.2?
D89.2 is linked to 1 UMLS Concept Unique Identifier: C0494269. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does D89.2 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like hypergammaglobulinemia, unspecified 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 D89.2?
D89.2 maps to the ICD-11 code: 4B2Y (Other specified disorders involving the immune system).
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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.