Search results for kcnq5

#	Family	MCID	Name	MIFTS	Score
1	c	INT555	Intellectual Developmental Disorder, Autosomal Dominant 46	30	43.363

2	P	MYP006	Myopia	56	13.883

3	P	DVL113	Developmental and Epileptic Encephalopathy	51	9.681

4	P	BNG026	Benign Neonatal Seizures	51	9.507

5		BNG006	Benign Familial Neonatal Epilepsy	53	9.485

6	c	ATS203	Autosomal Dominant Non-Syndromic Intellectual Disability	34	9.069

7	P	LNG028	Long Qt Syndrome	63	8.523

8	c	LNG044	Long Qt Syndrome 1	67	8.397

9		BNG009	Benign Epilepsy with Centrotemporal Spikes	59	8.334

10		NNT041	Neonatal Period Electroclinical Syndrome	23	8.181

11		HYP005	Hypokalemia	56	4.583

12		DFF043	Diffuse Gastric and Lobular Breast Cancer Syndrome	68	2.383

13	c	CLR087	Colorectal Cancer 12	34	2.383

14	c	PLY162	Polyposis Syndrome, Hereditary Mixed, 1	62	2.383

15		SML009	Small Intestine Adenocarcinoma	61	2.383

16	P	EPL164	Epilepsy	71	2.121

17	P	PRS040	Prostate Cancer	97	1.783

18		RFR003	Refractive Error	47	1.528

19	P	ENC018	Encephalopathy	64	1.437

20		PRP026	Peripheral Retinal Degeneration	45	1.386

21	P	RTN016	Retinal Degeneration	52	1.386

22	P	RTN008	Retinitis Pigmentosa	80	1.347

23		RTN023	Retinitis	47	1.347

24		CNV009	Convulsions Benign Familial Neonatal Dominant Form	27	1.304

25	P	CLR023	Colorectal Cancer	100	1.233