Search results for "[genes] WFS1"

32 hits were found for '[genes] WFS1'

# Family MCID Name MIFTS Score
1
P WLF004 Wolfram Syndrome 62 30.522
2
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 19.586
3
c CTR136 Cataract 41 17 19.586
4
P DBT005 Diabetes Insipidus 46 18.133
5
c WLF011 Wolfram-Like Syndrome, Autosomal Dominant 24 18.133
6
SNS001 Sensorineural Hearing Loss 49 16.553
7
WFS001 Wfs1-Related Disorders 10 16.553
8
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 14.805
9
INS001 Insulinoma 46 14.805
10
ADT003 Auditory System Disease 42 14.805
11
GLC008 Glucose Metabolism Disease 30 14.805
12
P NCL005 Nuclear Cataract 29 14.805
13
c DFN193 Deafness, Autosomal Dominant 6/14/38 23 14.805
14
WLF002 Wolf-Hirschhorn Syndrome 52 12.822
15
ASP001 Asperger Syndrome 43 12.822
16
P ACQ009 Acquired Metabolic Disease 27 12.822
17
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 24 12.822
18
DFN045 Dfna 6/14/38 Nonsyndromic Hearing Loss and Deafness 10 12.822
19
c WLF010 Wolfram Syndrome-Like Disease 10 12.822
20
DBT087 Diabetes Insipidus, Neurohypophyseal 51 10.469
21
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 50 10.469
22
c OPT055 Optic Atrophy Plus Syndrome 43 10.469
23
OPT006 Optic Nerve Disease 39 10.469
24
INN002 Inner Ear Disease 38 10.469
25
WTR001 Waterhouse-Friderichsen Syndrome 33 10.469
26
URN009 Urinary System Disease 33 10.469
27
c WLF009 Wolfram Syndrome 2 30 10.469
28
CRN031 Cranial Nerve Disease 30 10.469
29
CHR247 Chromosome 4p Deletion 18 10.469
30
NNS034 Non-Syndromic Congenital Cataract 20 7.403
31
DFN062 Dfna6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss 10 7.403
32
NNS015 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant 6 7.403