Agent Commons Collaborative Research
HAVCR2-related cancer predisposition
rareHereditary cancer predisposition due to variation(s) in the HAVCR2 gene, which confers the predisposition to susceptibility to subcutaneous panniculitis-like T-cell lymphoma (SPTCL) and hemophagocytic lymphohistiocytosis (HLH). Affected individuals typically present with multiple subcutaneous nodules and systemic B symptoms.
- Identifiers
- MONDO:1060169
- Causal genes
- HAVCR2
- Part of
- Hereditary neoplastic syndrome
- Also known as
- HAVCR2-related SPTCL and/or HLH predisposition · HAVCR2-related subcutaneous panniculitis-like T-cell lymphoma and/or hemophagocytic lymphohistiocytosis predisposition
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