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Summary Literature (0)
MIM:613101 - HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5, WITH OR WITHOUT MICROVILLUS INCLUSION DISEASE; FHL5

Xenbase Genes: stxbp2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009974 - lumen of Rathke's pouch
MONDO:0013135 - familial hemophagocytic lymphohistiocytosis 5

Disease Ontology (DO):
DOID:0110925 - familial hemophagocytic lymphohistiocytosis 5