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DOID:0110925 - familial hemophagocytic lymphohistiocytosis 5
Disease Ontology Definition:A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of the STXBP2 gene on chromosome 19p13.2.
Synonyms: FHL5, HLH5, HPLH5,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0013135 - familial hemophagocytic lymphohistiocytosis 5 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee