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) 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
- 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
Frequently Asked Questions
What is ICD-10 code D89.2?
ICD-10-CM code D89.2 represents "Hypergammaglobulinemia, unspecified". It 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.
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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.