Search results for "[genes] GSN"

34 hits were found for '[genes] GSN'

# Family MCID Name MIFTS Score
1
P AMY084 Amyloidosis, Finnish Type 35 22.044
2
P AMY004 Amyloidosis 59 20.784
3
P BRS047 Breast Cancer 100 17.999
4
CRN025 Corneal Dystrophy 36 16.431
5
P LTT001 Lattice Corneal Dystrophy 34 16.431
6
P TBR001 Tuberous Sclerosis 60 14.696
7
P PLY019 Polyneuropathy 42 14.696
8
c HRD039 Hereditary Amyloidosis 41 14.696
9
c FML249 Familial Amyloidosis, Finnish Type 21 14.696
10
CYS001 Cystic Fibrosis 84 12.727
11
INC002 Inclusion Body Myositis 63 12.727
12
P CRB019 Cerebral Amyloid Angiopathy 56 12.727
13
TCK001 Tick-Borne Encephalitis 48 12.727
14
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 40 12.727
15
CRN024 Corneal Disease 34 12.727
16
CRN106 Corneal Dystrophy, Gelatinous Drop-Like 29 12.727
17
MCL002 Macular Corneal Dystrophy 47 10.392
18
c TYR013 Tyrosinemia, Type Ii 47 10.392
19
FCL012 Facial Paralysis 43 10.392
20
P AMY082 Amyloidosis, Familial Visceral 40 10.392
21
c MYP082 Myopathy, Myofibrillar, 2 38 10.392
22
CRP017 Carpal Tunnel Syndrome, Familial 37 10.392
23
RHM008 Rheumatic Myocarditis 35 10.392
24
CRN247 Corneal Dystrophy, Thiel-Behnke Type 32 10.392
25
BLP001 Blepharochalasis 32 10.392
26
CHN008 Chandler Syndrome 30 10.392
27
c CRN236 Corneal Dystrophy, Lattice Type I 30 10.392
28
FCL011 Facial Nerve Disease 29 10.392
29
NRV004 Nerve Compression Syndrome 26 10.392
30
RDL004 Radial Neuropathy 26 10.392
31
c LTT008 Lattice Corneal Dystrophy Type Ii 23 10.392
32
AMY005 Amyloid Neuropathy 21 10.392
33
EPT024 Epithelial-Stromal Tgfbi Dystrophy 12 10.392
34
AGL003 Agel Amyloidosis 17 7.348