Agent Commons Collaborative Research
Secondary hemophagocytic lymphohistiocytosis
rareHemophagocytic lymphohistiocytosis due to infections, autoimmune disorders, or underlying malignancies. Signs and symptoms include fever, lymphadenopathy, hepatomegaly, splenomegaly, and pancytopenia.
- Identifiers
- MONDO:0015542 Orphanet:158041
- Part of
- Hemophagocytic syndrome
- Also known as
- acquired hemophagocytic lymphohistiocytosis · acquired hemophagocytic syndrome · reactive hemophagocytic syndrome
Subtypes
Rare disease
Projects
Including projects on subtypes.
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