Disease Details | GeDiPNet - Gene Disease Associations & Pathways

Disease Term	Disease ID	Gene Symbol	Classification	References	Source
CARDIOMYOPATHY	EFO_0000318	VCL	Unknown	39024449	GWAS catalog
CARDIOMYOPATHY, ALCOHOLIC	C0007192 MESH:D002310	AGT	Unknown	22497828	CTD Disgenet
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27	MONDO:0054838	ALPK3	Causal	21441111 26846950 27106955 27106995 85360505	ClinVar Disgenet
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1	C3495498 192600 MESH:C566005	ACTN2	Unknown	—	Disgenet
		ANKRD1	Unknown	—	Disgenet
		CACNA1C	Unknown	—	Disgenet
		CAV3	Unknown	—	CTD Disgenet HPO
		CSRP3	Unknown	—	Disgenet
		GLA	Unknown	—	Disgenet
		JPH2	Unknown	—	Disgenet
		LAMA4	Unknown	—	Disgenet
		LDB3	Unknown	—	Disgenet
		LMNA	Unknown	—	Disgenet
		LZTR1	Unknown	—	Disgenet
		MYBPC3	Unknown	—	Disgenet
		MYH6	Unknown	—	CTD Disgenet HPO
		MYH7	Unknown	—	CTD Disgenet HPO
		MYH7B	Unknown	—	Disgenet
		MYL2	Unknown	—	Disgenet
		MYL3	Unknown	—	Disgenet
		MYLK2	Unknown	—	CTD Disgenet HPO
		MYPN	Unknown	—	Disgenet
		NEXN	Unknown	—	Disgenet
		OBSCN	Unknown	—	Disgenet
		OXTR	Unknown	—	Disgenet
		PRKAG2	Unknown	—	Disgenet
		RAF1	Unknown	—	Disgenet
		RPL36A-HNRNPH2	Unknown	—	Disgenet
		SSUH2	Unknown	—	Disgenet
		TCAP	Unknown	—	Disgenet
		TNNI3	Unknown	—	Disgenet
		TNNT2	Unknown	—	Disgenet
		TPM1	Unknown	—	Disgenet
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10	608758 C1834460 MESH:C563865	MYL2	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11	612098 C2677506 MESH:C567419	ACTC1	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 12	612124 C2677491 OMIM:612124	CSRP3	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 13	613243 C2750472 MESH:C567686	TNNC1	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14	C2750467 613251 MESH:C567684	LDB3	Unknown	—	Disgenet
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14	C2750467 613251 MESH:C567684	MYH6	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 15	613255 C2750459 MESH:C567681	VCL	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16	613838 C3151204 OMIM:613838	MYOZ2	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 17	613873 C3151264 OMIM:613873	JPH2	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18	C3151265 613874 OMIM:613874	CEP85L	Unknown	—	Disgenet
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 18	C3151265 613874 OMIM:613874	PLN	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2	115195 C1861864 MESH:C566171	TNNT2	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2	115195 C1861864 MESH:C566171	TTN	Unknown	—	Disgenet
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 20	613876 C3151267 OMIM:613876	NEXN	Unknown	—	CTD Disgenet HPO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 21	C3553442	TPM1	Unknown	—	Disgenet
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22	C3714998	MYPN	Unknown	—	Disgenet
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 23, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION	C4225649	ACTN2	Unknown	—	Disgenet

«‹1…3 45›»

Cardiomyopathy