HAVCR2-related cancer predisposition

MONDO:1060169

Hereditary 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.

Also known as: HAVCR2-related SPTCL and/or HLH predisposition, HAVCR2-related subcutaneous panniculitis-like T-cell lymphoma and/or hemophagocytic lymphohistiocytosis predisposition

32 clinical trials for this condition and its sub-types, 0 tagged with HAVCR2-related cancer predisposition itself.

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↑ Hereditary neoplastic syndrome (731)

Including sub-types (32) Tagged with HAVCR2-related cancer predisposition (0)

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