Search results for "[genes] WFS1"

28 hits were found for '[genes] WFS1'

# Family MCID Name MIFTS Score
1
P WLF004 Wolfram Syndrome 62 30.000
2
c WLF011 Wolfram-Like Syndrome, Autosomal Dominant 25 19.843
3
c CTR136 Cataract 41 23 19.843
4
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 16.770
5
P DBT005 Diabetes Insipidus 53 16.770
6
WFS001 Wfs1-Related Disorders 8 16.770
7
SNS001 Sensorineural Hearing Loss 52 15.000
8
c DFN193 Deafness, Autosomal Dominant 6/14/38 19 15.000
9
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 12.990
10
WLF002 Wolf-Hirschhorn Syndrome 50 12.990
11
INS001 Insulinoma 60 12.990
12
c OPT055 Optic Atrophy Plus Syndrome 55 10.607
13
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 48 10.607
14
DBT087 Diabetes Insipidus, Neurohypophyseal 58 10.607
15
CHR247 Chromosome 4p Deletion 20 10.607
16
WTR001 Waterhouse-Friderichsen Syndrome 33 10.607
17
OPT006 Optic Nerve Disease 47 10.607
18
c WLF009 Wolfram Syndrome 2 35 10.607
19
CRN031 Cranial Nerve Disease 39 10.607
20
DFN062 Dfna6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss 10 10.607
21
NNS015 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant 6 10.607
22
ADT003 Auditory System Disease 49 7.500
23
INN002 Inner Ear Disease 48 7.500
24
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 26 7.500
25
DFN045 Dfna 6/14/38 Nonsyndromic Hearing Loss and Deafness 8 7.500
26
ATS009 Autosomal Genetic Disease 38 7.500
27
P ERL043 Early-Onset Nuclear Cataract 19 7.500
28
c WLF010 Wolfram Syndrome-Like Disease 9 7.500