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Familial hemophagocytic lymphohistiocytosis
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
No genes found
No SNPs found
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PBMC gene expression in children with active familial hemophagocytic lymphohistiocytosis (FHL)
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Literature
Most Relevant Literature
Novel STXBP2 mutation causing familial hemophagocytic lymphohistiocytosis.
Spinal cord involvement in a child with familial hemophagocytic lymphohistiocytosis.
Treatment of familial hemophagocytic lymphohistiocytosis with third-party mesenchymal stromal cells.
Familial hemophagocytic lymphohistiocytosis may present during adulthood: clinical and genetic featu…
Type III familial hemophagocytic lymphohistiocytosis susceptibility gene UNC13D involves in homologo…
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Most Relevant Clinical Trials
Treatment of Familiar Lymphohistiocytosis
Combination Chemotherapy Followed By Donor Stem Cell Transplant in Treating Patients With Hemophagoc…
Hybrid Immunotherapy for Hemophagocytic LymphoHistiocytosis
Pilot Study of Unrelated Donor Hematopoietic Stem Cell Transplantation in Patients With Life Threate…
Secondary Adult's Hemophagocytic Lymphohistiocytosis and Innate Immunity
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