Search results for "[genes] WFS1"

29 hits were found for '[genes] WFS1'

# Family MCID Name MIFTS Score
1
P WLF004 Wolfram Syndrome 59 30.009
2
c CTR136 Cataract 41 17 19.849
3
c WLF011 Wolfram-Like Syndrome, Autosomal Dominant 26 18.377
4
P DBT085 Diabetes Mellitus, Insulin-Dependent 77 16.776
5
P DBT005 Diabetes Insipidus 46 16.776
6
SNS001 Sensorineural Hearing Loss 44 16.776
7
INS001 Insulinoma 49 15.004
8
c DFN193 Deafness, Autosomal Dominant 6/14/38 19 15.004
9
WFS001 Wfs1-Related Disorders 9 15.004
10
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 76 12.994
11
WLF002 Wolf-Hirschhorn Syndrome 51 12.994
12
ASP001 Asperger Syndrome 44 12.994
13
DFN045 Dfna 6/14/38 Nonsyndromic Hearing Loss and Deafness 9 12.994
14
DBT087 Diabetes Insipidus, Neurohypophyseal 49 10.610
15
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 43 10.610
16
c OPT055 Optic Atrophy Plus Syndrome 40 10.610
17
INN002 Inner Ear Disease 38 10.610
18
WTR001 Waterhouse-Friderichsen Syndrome 38 10.610
19
OPT006 Optic Nerve Disease 35 10.610
20
CRN031 Cranial Nerve Disease 31 10.610
21
c WLF009 Wolfram Syndrome 2 29 10.610
22
CHR247 Chromosome 4p Deletion 18 10.610
23
c WLF010 Wolfram Syndrome-Like Disease 11 10.610
24
ADT003 Auditory System Disease 37 7.502
25
ATS009 Autosomal Genetic Disease 31 7.502
26
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 26 7.502
27
P ERL043 Early-Onset Nuclear Cataract 20 7.502
28
DFN062 Dfna6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss 10 7.502
29
NNS015 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant 5 7.502