Search results for "[genes] WFS1"

33 hits were found for '[genes] WFS1'

# Family MCID Name MIFTS Score
1
P WLF004 Wolfram Syndrome 61 29.417
2
c CTR136 Cataract 41 25 20.801
3
c WLF011 Wolfram-Like Syndrome, Autosomal Dominant 24 19.458
4
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 18.014
5
INS001 Insulinoma 61 18.014
6
SNS001 Sensorineural Hearing Loss 57 16.445
7
P DBT005 Diabetes Insipidus 53 16.445
8
c DFN193 Deafness, Autosomal Dominant 6/14/38 21 16.445
9
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 14.709
10
c OPT055 Optic Atrophy Plus Syndrome 52 14.709
11
WLF002 Wolf-Hirschhorn Syndrome 49 14.709
12
c WLF009 Wolfram Syndrome 2 45 14.709
13
WFS001 Wfs1-Related Disorders 7 14.709
14
OPT006 Optic Nerve Disease 52 12.738
15
CRN031 Cranial Nerve Disease 40 12.738
16
c ATS342 Autosomal Dominant Nonsyndromic Deafness 6 28 12.738
17
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 26 12.738
18
P ERL043 Early-Onset Nuclear Cataract 20 12.738
19
CHR247 Chromosome 4p Deletion 18 12.738
20
NNS015 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant 16 12.738
21
c WLF010 Wolfram Syndrome-Like Disease 13 12.738
22
DFN062 Dfna6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss 11 12.738
23
DFN045 Dfna 6/14/38 Nonsyndromic Hearing Loss and Deafness 8 12.738
24
INN002 Inner Ear Disease 49 10.401
25
c DFN141 Deafness, Autosomal Recessive 12 42 10.401
26
c DFN131 Deafness, Autosomal Dominant 1 38 10.401
27
c DFN190 Deafness, Autosomal Dominant 2a 37 10.401
28
c DFN143 Deafness, Autosomal Recessive 16 36 10.401
29
c DFN137 Deafness, Autosomal Dominant 13 35 10.401
30
ATS009 Autosomal Genetic Disease 35 10.401
31
NNS014 Nonsyndromic Hearing Loss and Deafness 28 10.401
32
c DFN272 Deafness, Autosomal Dominant 54 21 10.401
33
c NNS007 Nonsyndromic Deafness 42 7.354