Search results for "[genes] WFS1"

24 hits were found for '[genes] WFS1'

# Family MCID Name MIFTS Score
1
P WLF004 Wolfram Syndrome 61 31.526
2
c CTR136 Cataract 41 26 20.230
3
c WLF011 Wolfram-Like Syndrome, Autosomal Dominant 24 20.230
4
c DFN193 Deafness, Autosomal Dominant 6/14/38 20 18.729
5
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 17.097
6
INS001 Insulinoma 59 17.097
7
SNS001 Sensorineural Hearing Loss 57 17.097
8
P DBT005 Diabetes Insipidus 53 17.097
9
WFS001 Wfs1-Related Disorders 7 17.097
10
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 13.244
11
c OPT055 Optic Atrophy Plus Syndrome 54 13.244
12
WLF002 Wolf-Hirschhorn Syndrome 45 13.244
13
OPT006 Optic Nerve Disease 51 10.813
14
CRN031 Cranial Nerve Disease 40 10.813
15
c WLF009 Wolfram Syndrome 2 35 10.813
16
CHR247 Chromosome 4p Deletion 17 10.813
17
DFN062 Dfna6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss 10 10.813
18
NNS015 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant 7 10.813
19
INN002 Inner Ear Disease 50 7.646
20
ATS009 Autosomal Genetic Disease 39 7.646
21
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 25 7.646
22
P ERL043 Early-Onset Nuclear Cataract 19 7.646
23
c WLF010 Wolfram Syndrome-Like Disease 9 7.646
24
DFN045 Dfna 6/14/38 Nonsyndromic Hearing Loss and Deafness 8 7.646