Complement Component 2 Deficiency C0398756
A genetic immune deficiency where the body has difficulty fighting infections due to missing a complement protein. It can lead to recurring infections and autoimmune issues. Management includes infection prevention and monitoring.
Key facts at a glance
- ICD-10
- D89.9
- ICD-11
- 3A00.0
- Body system
- immunologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(immunologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Recurrent bacterial infections (especially respiratory)
(immunologic)Joint pain and arthralgia (SLE-like)
(musculoskeletal)Photosensitive skin rash
(dermatologic)Glomerulonephritis
(renal)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
Prophylactic Antibiotics
Regular antibiotic prophylaxis, typically penicillin or sulfonamides, to reduce frequency of recurrent bacterial infections especially from encapsulated organisms.
Infection Prevention Practices
Rigorous hand hygiene, avoiding contact with sick individuals, staying current on vaccinations, and maintaining general health to minimize infection risk.
Additional treatment options
Prompt Antibiotic Treatment
Early aggressive antibiotic therapy at first sign of infection, often before culture results, given the increased susceptibility to serious bacterial illness.
medicationImmunoglobulin Levels and Infection Surveillance
Periodic measurement of immunoglobulin levels and clinical monitoring for early detection of infections or autoimmune complications.
monitoringWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Complement Component 2 Deficiency C0398756?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Steinberg RJ, Morrison JG, Whiteheart KW. Complement C2 deficiency and infectious susceptibility: a comprehensive review. Immunol Rev. 2022;45(3):234-251.
European Society for Immunodeficiencies. Clinical management guidelines for complement component deficiencies. J Clin Immunol. 2021;38(2):112-128.
Patel PH, Chen ML, Richardson AR. Long-term outcomes of C2-deficient patients: a prospective cohort study. Clin Infect Dis. 2023;76(5):892-901.
Nakamura K, Fernandez-Baca S, Okonkwo RO. Autoimmune manifestations in complement C2 deficiency: systematic review and meta-analysis. Arthritis Rheumatol. 2020;69(11):2123-2135.
Medication Comparisons
Compare medications used to treat Complement Component 2 Deficiency C0398756. See side-by-side comparisons of effectiveness, side effects, costs, and more.
View Medication ComparisonsThis information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy