Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
FAMILIAL MENINGIOMA	MONDO:0011789	NF2	Causal	—	ClinVar GenCC
		PTEN	Causal	—	ClinVar
		SMARCE1	Causal	—	ClinGen ClinVar GenCC
		SUFU	Causal	—	ClinVar
		MN1	Unknown	—	ClinVar GenCC
		PDGFB	Unknown	—	ClinVar GenCC
FAMILIAL MULTIPLE MENINGIOMA	263662 MONDO:0016995	MN1	Unknown	—	Orphanet
		PDGFB	Unknown	3969118	Orphanet
		SMARCB1	Unknown	20930055	GWAS catalog Orphanet
		SMARCE1	Unknown	23377182	GWAS catalog Orphanet
		SUFU	Unknown	22958902	Orphanet
MENINGIOMA	2495 MESH:D008579MONDO_0016642MONDO:0016642	AKT1	Causal	23334667 31750041	CTD Orphanet
		NF2	Causal	23334667 8162072	CTD Orphanet
		PDGFB	Causal	2212004	Orphanet
		SMARCB1	Causal	20930055	Orphanet
		SMO	Causal	23334667 23348505	CTD Orphanet
		ALAD	Unknown	16140629	CTD
		BAP1	Unknown	25231345 28170043	CTD Orphanet
		CST3	Unknown	19747051	CTD
		CSTB	Unknown	19747051	CTD
		CTSL	Unknown	19747051	CTD
		GREB1	Unknown	39002029	GWAS catalog
		HES1	Unknown	21127729	CTD
		MLLT10	Unknown	21804547	CTD GWAS catalog
		NLRP6	Unknown	29762745	GWAS catalog
		NTHL1	Unknown	—	GenCC
		PGR	Unknown	19731987 19747051 8008172	CTD
		PIK3CA	Unknown	26826201	Orphanet
		PTEN	Unknown	12085208	CTD
		SEC11A	Unknown	39002029	GWAS catalog
		SMARCE1	Unknown	23377182 35681054	CTD Orphanet
		SUFU	Unknown	22958902	Orphanet
		TERT	Unknown	29216385 29312603	Orphanet
		TRAF7	Unknown	23334667 23348505	Orphanet
MENINGIOMA, FAMILIAL	MESH:C537443	MN1	Unknown	—	CTD
		NF2	Unknown	—	CTD
		PDGFB	Unknown	—	CTD
		PTEN	Unknown	—	CTD
		SMARCE1	Unknown	23377182	CTD
		SUFU	Unknown	—	CTD
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO	607174	MN1	Unknown	—	HPO
		NF2	Unknown	—	HPO
		PDGFB	Unknown	—	HPO

Meningioma