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Disease Ontology Browser
familial hemophagocytic lymphohistiocytosis 5 (DOID:0110925)
Alliance: disease page
Synonyms: FHL5; HLH5; HPLH5
Alt IDs: OMIM:613101
Definition: A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of STXBP2 on chromosome 19p13.2.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory