Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
VON WILLEBRAND DISEASE	C0042974	F3	Unknown	—	Disgenet
		GP1BA	Unknown	—	Disgenet
		GP6	Unknown	—	Disgenet
		P2RY12	Unknown	—	Disgenet
		VWF	Unknown	—	Disgenet
VON WILLEBRAND DISEASE 1	MONDO:0008668	VWF	Unknown	10669167 14613933 16870550 19060241 19506356 20303469 21206511 21346256 21711445 23406206 25690668 25696906 25756206 26843468	CTD
VON WILLEBRAND DISEASE 2	MONDO:0013304	VWF	Unknown	—	GenCC
VON WILLEBRAND DISEASE 3	MONDO:0010191	VWF	Unknown	20301765	GenCC
VON WILLEBRAND DISEASE TYPE 1	166078	VWF	Causal	20301765	ClinVar Orphanet
VON WILLEBRAND DISEASE TYPE 2		VWF	Causal	—	ClinVar
VON WILLEBRAND DISEASE TYPE 2A	166084 MONDO:0015628	VWF	Causal	20301765	GWAS catalog Orphanet
VON WILLEBRAND DISEASE TYPE 2B	166087 MONDO:0015629	VWF	Causal	108291 1373334 1419803 1672694 2010538 2011604 20200350 20301765 20371742 27212476 8075643 8123843 8376405 8547152 9858249	ClinGen GWAS catalog Orphanet
VON WILLEBRAND DISEASE TYPE 2M	166090 C1282974 MONDO:0015630	VWF	Causal	20301765	Disgenet Orphanet
VON WILLEBRAND DISEASE TYPE 2N	166093 MONDO:0015631	VWF	Causal	20301765	GWAS catalog Orphanet
VON WILLEBRAND DISEASE TYPE 3	166096	VWF	Causal	20301765	ClinVar Orphanet
VON WILLEBRAND DISEASE, PLATELET TYPE	C1280798 MESH:C536458	GP1BA	Unknown	—	CTD Disgenet
VON WILLEBRAND DISEASE, PLATELET-TYPE	177820	GP1BA	Unknown	—	HPO
VON WILLEBRAND DISEASE, TYPE 1	C1264039 193400 MESH:D056725	CDH15	Unknown	—	Disgenet
		ITGA2	Unknown	—	Disgenet
		ITGA2B	Unknown	—	Disgenet
		PLAT	Unknown	—	Disgenet
		VWF	Unknown	—	CTD Disgenet HPO
VON WILLEBRAND DISEASE, TYPE 2	C1264040 613554 MESH:D056728	ITGA2	Unknown	—	Disgenet
VON WILLEBRAND DISEASE, TYPE 2	C1264040 613554 MESH:D056728	VWF	Unknown	—	CTD Disgenet HPO
VON WILLEBRAND DISEASE, TYPE 2A	C1282968	VWF	Unknown	—	Disgenet
VON WILLEBRAND DISEASE, TYPE 2B	C1282971	VWF	Unknown	—	Disgenet
VON WILLEBRAND DISEASE, TYPE 2N	C1282975	VWF	Unknown	—	Disgenet
VON WILLEBRAND DISEASE, TYPE 3	277480 C1264041 MESH:D056729	VWF	Unknown	—	CTD Disgenet HPO

Von willebrand disorder