Search results for kcnq4

#	Family	MCID	Name	MIFTS	Score
1	c	DFN190	Deafness, Autosomal Dominant 2a	38	44.217

2		DFN001	Dfna2 Nonsyndromic Hearing Loss	13	31.246

3	P	NNS072	Nonsyndromic Hearing Loss	43	23.370

4		RRG078	Rare Genetic Deafness	37	22.105

5		NNS044	Non-Syndromic Genetic Deafness	44	20.683

6	P	SNS001	Sensorineural Hearing Loss	59	19.157

7		DFN245	Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct	53	9.626

8	P	LNG028	Long Qt Syndrome	63	8.511

9	c	DFN136	Deafness, Autosomal Dominant 9	46	8.426

10	c	LNG044	Long Qt Syndrome 1	67	8.381

11		ATS251	Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna	27	8.222

12	c	ATS005	Autosomal Dominant Nonsyndromic Deafness	27	7.835

13		BNG006	Benign Familial Neonatal Epilepsy	53	7.155

14	P	BNG026	Benign Neonatal Seizures	51	7.155

15		MNR012	Meniere Disease	56	6.962

16	c	DFN097	Deafness, Autosomal Recessive 1a	51	6.914

17	c	BRN131	Branchiootorenal Syndrome 1	46	6.914

18	c	USH036	Usher Syndrome, Type I	63	6.851

19	c	DFN196	Deafness, Autosomal Dominant 22	45	6.851

20	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	6.732

21	c	WRD030	Waardenburg Syndrome, Type 1	55	6.699

22	c	DFN118	Deafness, Autosomal Dominant 44	29	6.699

23	c	DFN165	Deafness, Autosomal Recessive 14	19	6.699

24	c	DFN107	Deafness, Autosomal Dominant 10	40	6.699

25	c	DFN155	Deafness, Autosomal Dominant 41	34	6.699