Fanconi Anemia Complementation Group S C4554406
A rare genetic disorder in the Fanconi anemia DNA repair pathway. It may lead to bone marrow problems and increased cancer susceptibility. Care includes regular blood monitoring and transplant when needed.
Key facts at a glance
- ICD-10
- D61.03
- ICD-11
- 3A00.0
- Body system
- hematologic
- Severity
- severe
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(hematologic)Significant symptoms that substantially affect daily functioning.
Frequency: Common at all stages
Pallor
(hematologic)Prolonged bleeding after cuts
(hematologic)Gingival bleeding
(hematologic)Renal anomalies
(hematologic)Medication Comparisons
Compare medications used to treat Fanconi Anemia Complementation Group S C4554406. 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.
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy