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Summary Literature (0)
DOID:0110924 - familial hemophagocytic lymphohistiocytosis 4

Disease Ontology Definition:A hemophagocytic lymphohistiocytosis that has_material_basis_in an autosomal recessive mutation of the STX11 gene on chromosome 6q24.2.

Synonyms: FHL4, HLH4, HPLH4

Xenbase Genes : stx11

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011336 - familial hemophagocytic lymphohistiocytosis 4

MIM:
MIM:603552 - HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4; FHL4

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), hemophagocytic lymphohistiocytosis (is_a)