Search results for kcnq4

119 hits were found for kcnq4

#	Family	MCID	Name	MIFTS	Score
1		ATS251	Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna	38	64.063

2	c	DFN190	Deafness, Autosomal Dominant 2a	37	49.458

3		DFN001	Dfna2 Nonsyndromic Hearing Loss	12	36.019

4	P	NNS072	Nonsyndromic Hearing Loss	40	29.776

5	P	SNS001	Sensorineural Hearing Loss	59	22.680

6		RRG078	Rare Genetic Deafness	29	21.199

7		NNS044	Non-Syndromic Genetic Deafness	30	20.821

8		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	14.791

9	c	NNS007	Nonsyndromic Deafness	33	14.243

10	c	BRN108	Branchiootic Syndrome 1	62	13.071

11	P	LNG028	Long Qt Syndrome	64	10.903

12	c	LNG044	Long Qt Syndrome 1	66	10.386

13		DFN245	Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct	50	9.465

14	c	ATS005	Autosomal Dominant Nonsyndromic Deafness	24	9.465

15	c	DFN136	Deafness, Autosomal Dominant 9	44	9.378

16		MNR012	Meniere Disease	56	7.612

17	P	BRN042	Branchiootic Syndrome	41	7.612

18	P	BNG026	Benign Neonatal Seizures	49	7.343

19	c	DFN118	Deafness, Autosomal Dominant 44	27	6.692

20	c	DFN107	Deafness, Autosomal Dominant 10	40	6.692

21	c	DFN353	Deafness, Autosomal Dominant 12	38	6.692

22	c	DFN351	Deafness, Autosomal Dominant 6	42	6.692

23	c	DFN137	Deafness, Autosomal Dominant 13	32	6.692

24	c	DFN117	Deafness, Autosomal Dominant 15	38	6.692

25	P	YLN002	Y-Linked Monogenic Disease	17	6.692

26	c	DFN099	Deafness, Autosomal Dominant 2b	30	6.692

27	c	DFN255	Deafness, Autosomal Dominant 64	26	6.692

28	P	USH001	Usher Syndrome	64	6.692

29	c	FML001	Familial Atrial Fibrillation	65	6.692

30	c	DFN189	Deafness, Autosomal Dominant 25	39	6.692

31	c	DFN149	Deafness, Autosomal Dominant 18	25	6.692

32	c	DFN200	Deafness, Autosomal Dominant 17	43	6.692

33	c	DFN354	Deafness, Autosomal Dominant 20	41	6.692

34	c	DFN165	Deafness, Autosomal Recessive 14	19	6.692

35	c	DFN148	Deafness, Autosomal Dominant 16	29	6.692

36	c	DFN094	Deafness, Autosomal Dominant 28	31	6.692

37	c	DFN097	Deafness, Autosomal Recessive 1a	46	6.692

38	c	DFN155	Deafness, Autosomal Dominant 41	34	6.692

39	c	DFN128	Deafness, Autosomal Dominant 36	39	6.692

40		ACT032	Acute Hemorrhagic Leukoencephalitis	33	6.692

41	c	DFN166	Deafness, Autosomal Recessive 17	23	6.692

42	P	WRD001	Waardenburg's Syndrome	60	6.692

43	P	INN002	Inner Ear Disease	50	6.692

44		ADT003	Auditory System Disease	49	6.692

45		VST004	Vestibular Disease	40	6.692

46		BNG009	Benign Epilepsy with Centrotemporal Spikes	60	6.692

47		PRP028	Peripheral Vertigo	37	6.692

48		HLX001	Helix Syndrome	48	3.771

49	P	JRV004	Jervell and Lange-Nielsen Syndrome 1	56	3.693

50		HRN029	Hearing Loss, Noise-Induced	37	3.117

51	c	WLF013	Wolfram Syndrome 1	60	2.723

52	P	VSC007	Vascular Disease	63	2.365

53	P	ALC033	Alcohol Use Disorder	61	2.226

54		KCN010	Kcnq2-Related Disorders	24	2.073

55		KCN014	Kcnq3-Related Disorders	9	2.073

56		MTN003	Motion Sickness	51	1.899

57	c	DFN114	Deafness, Autosomal Recessive 67	35	1.899

58		BNG006	Benign Familial Neonatal Epilepsy	55	1.839

59	P	EPL164	Epilepsy	68	1.592

60		AGR019	Age-Related Hearing Loss	41	1.592

61	P	PLM037	Pulmonary Hypertension	72	1.454

62	c	DPH024	Diaphragmatic Hernia, Congenital	64	1.300

63		PRT037	Pertussis	65	1.126

64		ACS001	Acoustic Neuroma	56	1.126

65		NRL005	Neurilemmoma	60	1.126

66	P	ALZ034	Alzheimer Disease	87	0.919

67	P	EPL140	Epilepsy, Idiopathic Generalized	62	0.919

68		CRD223	Cardiac Arrhythmia	63	0.919

69	P	SCH015	Schizophrenia	74	0.919

70	c	ATR087	Atrial Standstill 1	74	0.919

71	c	BRN131	Branchiootorenal Syndrome 1	45	0.919

72		ATR057	Atrioventricular Block	54	0.919

73	c	LNG047	Long Qt Syndrome 2	59	0.919

74	P	BRN006	Branchiootorenal Syndrome	50	0.919

75	c	PRC016	Pre-Eclampsia	65	0.919

76	c	DLT002	Dilated Cardiomyopathy	78	0.919

77		IMP005	Impotence	52	0.919

78	P	HYP086	Hypothyroidism	69	0.919

79	P	SCK002	Sick Sinus Syndrome	55	0.919

80		IRR002	Irritable Bowel Syndrome	65	0.919

81		MST020	Mast Cell Activation Syndrome	28	0.919

82	c	GLM047	Glioma Susceptibility 3	33	0.803

83	c	MSM022	Mismatch Repair Cancer Syndrome 1	70	0.803

84	c	GLM025	Glioma Susceptibility 2	30	0.803

85	c	GLM043	Glioma Susceptibility 9	30	0.803

86	P	GLM040	Glioma Susceptibility 1	71	0.803

87		MNN043	Meningioma, Familial	79	0.803

88	P	OLG002	Oligodendroglioma	66	0.803

89		GLM045	Glioma	63	0.803

90	P	BRS047	Breast Cancer	98	0.779

91	c	USH036	Usher Syndrome, Type I	61	0.650

92		AGN016	Aging	54	0.650

93	c	DFN159	Deafness, Autosomal Dominant 5	31	0.650

94		ALC007	Alcohol Dependence	66	0.650

95	c	LNG050	Long Qt Syndrome 5	46	0.650

96	c	DFN178	Deafness, Autosomal Recessive 59	32	0.650

97	c	SZR022	Seizures, Benign Familial Neonatal, 1	43	0.650

98		ERM002	Ear Malformation	36	0.650

99	P	NRB001	Neuroblastoma	66	0.650

100		HYP066	Hyperglycemia	61	0.650

101	P	RTN016	Retinal Degeneration	52	0.650

102		HYP005	Hypokalemia	55	0.650

103		PPT005	Peptic Ulcer Disease	58	0.650

104		CNS004	Constipation	56	0.650

105	c	BSL007	Basal Cell Carcinoma	68	0.650

106	P	RNL007	Renal Tubular Acidosis	50	0.650

107	P	ECL001	Eclampsia	52	0.650

108	P	DRR001	Diarrhea	55	0.650

109		NNS008	Nonsyndromic Hearing Loss and Deafness, Dfna3	16	0.650

110	P	FBR031	Febrile Seizures	52	0.650

111		HYP266	Hypoxia	57	0.650

112	c	DFN027	Deafness, Autosomal Dominant Nonsyndromic Sensorineural 3	14	0.650

113	c	CNT101	Central Congenital Hypothyroidism	36	0.650

114		CNV009	Convulsions Benign Familial Neonatal Dominant Form	31	0.650

115	P	OVR042	Ovarian Cancer	88	0.551

116	P	PNC035	Pancreatic Cancer	86	0.551

117		MYL005	Myelofibrosis	71	0.551

118		NRL016	Neural Tube Defects	81	0.430

119	P	RNL017	Renal Oncocytoma	54	0.430