Von hippel-lindau syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
VON HIPPEL-LINDAU DISEASE
892MESH:D006623MONDO:0008667
CCND1 Unknown
12097293
CTD, GWAS catalog, Orphanet
Endocrine resistance FoxO signaling pathway Cell cycle +58 more
VHL Unknown
10533030 12414898 7784063 20583150 7563486 8550742 8956040 11171960 27964749 36444493 37580113 16502427 10408776 10627136 10635329 8493574 9452106 8825918 8592333 8730290 8634692 7728151 9829912 9452032 7987306 9829911
CTD, ClinGen, GWAS catalog, Orphanet
VON HIPPEL-LINDAU SYNDROME
C0019562
CCND1 Unknown — ClinVar, Disgenet
Endocrine resistance FoxO signaling pathway Cell cycle +58 more
MMP3 Unknown — Disgenet
All4 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Von hippel-lindau syndrome.
5 View disease cluster →
Chuvash erythrocytosis 1 shared geneVHL Related via 1 shared gene including VHL. Erythrocytosis due to tissue hypoxemia 1 shared geneVHL Related via 1 shared gene including VHL. Pancreatic cyst 1 shared geneVHL Related via 1 shared gene including VHL. Au-kline syndrome 1 shared geneVHL Related via 1 shared gene including VHL. Carney-stratakis syndrome 1 shared geneSDHB Related via 1 shared gene including SDHB.