Familial meningioma

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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • familial meningioma
MONDO_0011789
SMARCE1 Causal
23377182 25143307
ClinGen, Open Targets
  • familial meningioma
MONDO_0011789
SUFU Causal
19533801 25403219
Open Targets
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Familial meningioma.
5 View disease cluster →
Joubert syndrome with cranio-facial and skeletal defects 1 shared geneSUFU Related via 1 shared gene including SUFU. Joubert and congenital ocular motor apraxia 1 shared geneSUFU Related via 1 shared gene including SUFU. Cleft face 1 shared geneSMARCE1 Related via 1 shared gene including SMARCE1. Gorlin syndrome 1 shared geneSUFU Related via 1 shared gene including SUFU. Basal cell nevus syndrome 1 shared geneSUFU Related via 1 shared gene including SUFU.