Overview
Erythrophagocytosis is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Myelofibrosis
Excluded (<1%)
Chediak-Higashi syndrome
Very frequent (80-99%)
Graft versus host disease
Occasional (5-29%)
Adult onset Still's disease
Occasional (5-29%)
Lysinuric protein intolerance
Frequent (30-79%)
Familial haemophagocytic lymphohistiocytosis
Very frequent (80-99%)
Subcutaneous panniculitic cutaneous T-cell lymphoma
Frequent (30-79%)
Macrophage activation syndrome
Very frequent (80-99%)
Acquired hemophagocytic lymphohistiocytosis associated with malignant disease
Always present (100%)
X-linked lymphoproliferative syndrome type 1
Frequent (30-79%)
X-linked lymphoproliferative syndrome type 2
Frequent (30-79%)
Combined immunodeficiency due to IL2 inducible T cell kinase deficiency
Excluded (<1%)
Quick Facts
- SNOMED CT
- 61070002
- UMLS CUI
- C0302486
- Fully Specified Name
- Erythrophagocytosis (finding)
- Associated Conditions
- 12
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.