C203461Level 8
Familial Hemophagocytic Lymphohistiocytosis Type 4
**Semantic type:** Disease or Syndrome
**Definition:** Familial hemophagocytic lymphohistiocytosis caused by biallelic mutations in the STX11 gene.
**Synonyms:** - FHL4 - STX11-FHLH - STX11-Related Familial Hemophagocytic Lymphohistiocytosis - STX11-fHLH
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