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Immunodeficiency With Factor H Anomaly Cn293972

Published: July 22, 2026Updated: August 20, 2026

A genetic disorder affecting factor H, a protein that controls complement activity. This leads to complement dysregulation and increased infection risk. Treatment focuses on infection prevention and monitoring.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
D89.9
ICD-11
3A00.0
Body system
immunologic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Generalized symptoms

(immunologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Recurrent upper respiratory tract infections

(immunologic)

Persistent fatigue

(immunologic)

Autoimmune thrombocytopenia

(immunologic)

Opportunistic infection (Pneumocystis pneumonia)

(immunologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

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

1

Combination drug regimen with regular assessment

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
2

Eculizumab or Ravulizumab

Complement inhibitor therapy to address the factor H anomaly and prevent complement-mediated tissue damage.

medication
3

Antibiotic Prophylaxis

Preventive antibiotics to reduce infection risk, particularly against encapsulated bacteria.

medication

Additional treatment options

Complement and Renal Function Monitoring

Regular assessment of complement activity levels, renal function, and markers of hemolysis to evaluate disease control.

monitoring

Plasma Exchange

Therapeutic plasma exchange to remove pathogenic factors and replace deficient complement regulatory proteins.

procedure

Vaccination with Appropriate Vaccines

Completion of recommended vaccinations including pneumococcal, meningococcal, and Haemophilus influenzae vaccines.

lifestyle

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Immunodeficiency With Factor H Anomaly Cn293972?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Medication Comparisons

Compare medications used to treat Immunodeficiency With Factor H Anomaly Cn293972. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy