Search results for wfs1

#	Family	MCID	Name	MIFTS	Score
1	c	WLF013	Wolfram Syndrome 1	59	85.059

2	c	DFN351	Deafness, Autosomal Dominant 6	38	51.870

3	P	WLF004	Wolfram Syndrome	57	46.475

4	c	WLF011	Wolfram-Like Syndrome, Autosomal Dominant	35	40.796

5	c	CTR136	Cataract 41	23	34.222

6	c	TYP009	Type 2 Diabetes Mellitus	91	33.762

7	P	DBT009	Diabetes Mellitus	67	33.497

8	P	SNS001	Sensorineural Hearing Loss	59	28.350

9		WFS003	Wfs1 Spectrum Disorder	8	23.525

10		RRG078	Rare Genetic Deafness	37	22.286

11	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	66	21.879

12	P	DBT005	Diabetes Insipidus	55	20.594

13		HYD002	Hydronephrosis	58	15.643

14	P	NGH001	Night Blindness	52	14.871

15		INS001	Insulinoma	59	14.736

16	P	CTR002	Cataract	60	14.320

17	P	NNS072	Nonsyndromic Hearing Loss	43	13.873

18	P	BPL003	Bipolar Disorder	57	13.799

19	P	NRP001	Neuropathy	58	13.705

20	c	TYP008	Type 1 Diabetes Mellitus	79	13.096

21	P	SPS008	Spastic Ataxia	45	12.088

22	c	WLF009	Wolfram Syndrome 2	41	12.050

23		MNG006	Monogenic Diabetes	42	11.909

24		MDD011	Mood Disorder	61	11.771

25	P	OPT006	Optic Nerve Disease	56	9.837

The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z