Search results for "[genes] WFS1"

20 hits were found for '[genes] WFS1'

# Family MCID Name MIFTS Score
1
P WLF004 Wolfram Syndrome 61 54.603
2
c DFN193 Deafness, Autosomal Dominant 6/14/38 14 31.202
3
WFS001 Wfs1-Related Disorders 8 22.063
4
c WLF011 Wolfram-Like Syndrome, Autosomal Dominant 18 20.638
5
P DBT005 Diabetes Insipidus 53 19.107
6
INS001 Insulinoma 49 19.107
7
c CTR136 Cataract 41 14 19.107
8
SNS001 Sensorineural Hearing Loss 48 15.601
9
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 82 11.032
10
P NCL005 Nuclear Cataract 32 11.032
11
WTR001 Waterhouse-Friderichsen Syndrome 32 11.032
12
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 28 11.032
13
c WLF009 Wolfram Syndrome 2 26 11.032
14
DFN003 Deafness and Hereditary Hearing Loss 25 11.032
15
CHR247 Chromosome 4p Deletion 17 11.032
16
NNS034 Non-Syndromic Congenital Cataract 22 7.800
17
c WLF010 Wolfram Syndrome-Like Disease 10 7.800
18
NNS015 Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant 6 7.800
19
DFN045 Dfna 6/14/38 Nonsyndromic Hearing Loss and Deafness 4 7.800
20
DFN062 Dfna6/14/38 Nonsyndromic Low Frequency Sensorineural Hearing Loss 3 7.800