Search results for KCNE2

74 hits were found for KCNE2

#	Family	MCID	Name	MIFTS	Score
1	c	LNG051	Long Qt Syndrome 6	44	5.311

2	P	LNG028	Long Qt Syndrome	66	4.343

3	c	ATR039	Atrial Fibrillation, Familial, 4	21	4.283

4	c	FML001	Familial Atrial Fibrillation	65	3.885

5		CRD223	Cardiac Arrhythmia	60	3.642

6	P	ATR011	Atrial Fibrillation	66	3.518

7	P	HRT032	Heart Disease	75	3.368

8	c	FML191	Familial Long Qt Syndrome	53	3.338

9	c	LNG044	Long Qt Syndrome 1	66	3.325

10	c	DLT002	Dilated Cardiomyopathy	79	2.488

11	P	BRG001	Brugada Syndrome	71	2.488

12	P	HYP061	Hypertrophic Cardiomyopathy	70	2.457

13		ATR057	Atrioventricular Block	55	2.423

14		CNG034	Congestive Heart Failure	69	2.382

15	c	LNG048	Long Qt Syndrome 3	53	2.382

16		CRD054	Cardiac Arrhythmia, Ankyrin-B-Related	47	2.382

17	c	LNG047	Long Qt Syndrome 2	58	1.871

18	P	JRV004	Jervell and Lange-Nielsen Syndrome 1	56	1.813

19	c	LNG050	Long Qt Syndrome 5	46	1.813

20	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	1.779

21	c	SHR030	Short Qt Syndrome	46	1.738

22		WLF001	Wolff-Parkinson-White Syndrome	66	1.684

23	P	CNG001	Congenital Myasthenic Syndrome	66	1.684

24		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	1.684

25	P	CTC001	Catecholaminergic Polymorphic Ventricular Tachycardia	63	1.684

26		TMT001	Timothy Syndrome	61	1.684

27	c	MYS051	Myasthenic Syndrome, Congenital, 5	57	1.684

28	c	OST080	Osteogenesis Imperfecta, Type Ii	54	1.684

29		SNT005	Sinoatrial Node Disease	49	1.684

30	c	LNG056	Long Qt Syndrome 12	42	1.684

31	c	LNG045	Long Qt Syndrome 10	42	1.684

32	c	LNG053	Long Qt Syndrome 9	41	1.684

33	c	LNG057	Long Qt Syndrome 13	40	1.684

34	c	LNG046	Long Qt Syndrome 11	39	1.684

35	c	BRG003	Brugada Syndrome 3	39	1.684

36	c	DFN269	Deafness, Autosomal Recessive 98	35	1.684

37		HRT008	Heart Conduction Disease	32	1.684

38		INT084	Intrinsic Cardiomyopathy	28	1.684

39		SYN036	Syncope	45	0.171

40		CRD132	Cardiac Conduction Defect	58	0.129

41	P	GST053	Gastric Cancer	83	0.091

42		DFC004	Deficiency Anemia	70	0.091

43	P	HYP086	Hypothyroidism	69	0.091

44		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.091

45	c	BRN108	Branchiootic Syndrome 1	62	0.091

46	P	GST044	Gastritis	56	0.091

47	P	ALP008	Alopecia	54	0.091

48	P	HPT023	Hepatocellular Carcinoma	100	0.064

49	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.064

50		ACR007	Acromegaly	71	0.064

51	P	MYC007	Myocardial Infarction	70	0.064

52		GST040	Gastric Adenocarcinoma	70	0.064

53	P	LVR013	Liver Disease	68	0.064

54		HYP056	Hypoglycemia	66	0.064

55		ATH013	Atherosclerosis Susceptibility	65	0.064

56	P	DBT009	Diabetes Mellitus	64	0.064

57	P	ADN016	Adenocarcinoma	64	0.064

58		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.064

59		FTT001	Fatty Liver Disease	61	0.064

60		IRN001	Iron Deficiency Anemia	59	0.064

61		ADN018	Adenoma	59	0.064

62		HLC007	Helicobacter Pylori Infection	59	0.064

63		IRN002	Iron Metabolism Disease	57	0.064

64	c	ACT075	Acute Myocardial Infarction	57	0.064

65		HYP266	Hypoxia	57	0.064

66		GTR002	Goiter	53	0.064

67	P	GNG025	Gingival Fibromatosis	50	0.064

68		HLX001	Helix Syndrome	47	0.064

69		GRW007	Growth Hormone Deficiency	46	0.064

70		DWR001	Dwarfism	44	0.064

71		FBR019	Fibromatosis	41	0.064

72		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	41	0.064

73	P	LTH003	Lethal Congenital Contracture Syndrome	40	0.064

74		HRM003	Hormone Producing Pituitary Cancer	37	0.064