FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term familial hemophagocytic lymphohistiocytosis 4 ID (Ontology) DOID:0110924 (Human Disease)
Definition A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of the STX11 gene on chromosome 6q24.2.
Also Known As "FHL4" ; "HLH4" ; "HPLH4"
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DO.org
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 Genes
 familial hemophagocytic lymphohistiocytosis 4       1
 for disease ribbon | familial hemophagocytic lymphohistiocytosis 4       1
 model of | familial hemophagocytic lymphohistiocytosis 4       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease_________
lymphatic system disease                |
 |__hemophagocytic lymphohistiocytosis__|
                                        familial hemophagocytic lymphohistiocytosis 4  1 rec.
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Is a hemophagocytic lymphohistiocytosis
autosomal recessive disease
Part of
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Synonyms
  • "FHL4" EXACT OMO:0003012
    "HLH4" EXACT OMO:0003012
    "HPLH4" EXACT OMO:0003012
Secondary IDs
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GARD:9929
MIM:603552