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 3 ID (Ontology) DOID:0110923 (Human Disease)
Definition A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the UNC13D gene on chromosome 17q25.1.
Also Known As "FHL3" ; "HLH3" ; "HPLH3"
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DO.org
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 Genes
 familial hemophagocytic lymphohistiocytosis 3       1
 for disease ribbon | familial hemophagocytic lymphohistiocytosis 3       1
 model of | familial hemophagocytic lymphohistiocytosis 3       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease_________
lymphatic system disease                |
 |__hemophagocytic lymphohistiocytosis__|
                                        familial hemophagocytic lymphohistiocytosis 3  1 rec.
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Is a hemophagocytic lymphohistiocytosis
autosomal recessive disease
Part of
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Synonyms
  • "FHL3" EXACT OMO:0003012
    "HLH3" EXACT OMO:0003012
    "HPLH3" EXACT OMO:0003012
Secondary IDs
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GARD:9928
MIM:608898