Search results for "WFS1"

33 hits were found for 'WFS1'
Try searching for fs1

# Family MCID Name MIFTS Score
1
P WLF004 Wolfram Syndrome 70 13.640
2
c DFN193 Deafness, Autosomal Dominant 6/14/38 12 5.650
3
WFS001 Wfs1-Related Disorders 10 5.327
4
WLF011 Wolfram-Like Syndrome, Autosomal Dominant 10 5.039
5
c DBT009 Diabetes Mellitus 74 4.750
6
c OPT004 Optic Atrophy 50 4.726
7
P DBT005 Diabetes Insipidus 58 4.644
8
INS001 Insulinoma 59 4.613
9
c CTR136 Cataract 41 13 4.613
10
SNS001 Sensorineural Hearing Loss 57 3.997
11
c DMN027 Dominant Optic Atrophy 38 2.756
12
c WLF009 Wolfram Syndrome 2 25 2.714
13
c CHR247 Chromosome 4p Deletion 25 2.714
14
P CTR103 Cataract 4, Multiple Types 51 2.664
15
P DFN102 Deafness, Autosomal Dominant 3b 41 2.664
16
WTR001 Waterhouse-Friderichsen Syndrome 38 2.664
17
DBT047 Diabetes Mellitus, Noninsulin-Dependent, Association with 37 2.664
18
DFN003 Deafness and Hereditary Hearing Loss 29 2.664
19
P OP3001 Opa3-Related 3-Methylglutaconic Aciduria 56 1.883
20
c WLF010 Wolfram Syndrome-Like Disease 10 1.883
21
NNS015 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant 8 1.883
22
DFN045 Dfna 6/14/38 Nonsyndromic Hearing Loss and Deafness 5 1.883
23
DFN062 Dfna6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss 4 1.883
24
c PNC044 Pancreatitis 69 0.136
25
MDD011 Mood Disorder 53 0.111
26
c TYP009 Type 2 Diabetes Mellitus 100 0.079
27
P BPL003 Bipolar Disorder 77 0.079
28
P INS005 Insulin Resistance 65 0.079
29
NRP001 Neuropathy 62 0.079
30
WLF002 Wolf-Hirschhorn Syndrome 61 0.079
31
c CTR002 Cataract 57 0.079
32
RTN023 Retinitis 54 0.079
33
NRN002 Neuronitis 44 0.079