Hemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease

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Subtype of: Hemophagocytic lymphohistiocytosis
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • Hemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease
540
STXBP2 Unknown
19804848 19884660
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Hemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease.
5 View disease cluster →
Microvillus inclusion disease 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2. Congenital lactic acidosis 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2. Hereditary hemophagocytic lymphohistiocytosis 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2. Carotid artery thrombosis 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2. Hemophagocytic lymphohistiocytosis 1 shared geneSTXBP2 Related via 1 shared gene including STXBP2.