Search results for "[genes] GSN"

34 hits were found for '[genes] GSN'

# Family MCID Name MIFTS Score
1
P AMY084 Amyloidosis, Finnish Type 38 22.044
2
P AMY004 Amyloidosis 68 20.784
3
P BRS047 Breast Cancer 100 17.999
4
CRN025 Corneal Dystrophy 41 16.431
5
P LTT001 Lattice Corneal Dystrophy 35 16.431
6
P TBR001 Tuberous Sclerosis 69 14.696
7
P PLY019 Polyneuropathy 55 14.696
8
c HRD039 Hereditary Amyloidosis 49 14.696
9
c FML249 Familial Amyloidosis, Finnish Type 22 14.696
10
CYS001 Cystic Fibrosis 86 12.727
11
INC002 Inclusion Body Myositis 65 12.727
12
P CRB019 Cerebral Amyloid Angiopathy 56 12.727
13
TCK001 Tick-Borne Encephalitis 54 12.727
14
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 49 12.727
15
CRN024 Corneal Disease 46 12.727
16
CRN106 Corneal Dystrophy, Gelatinous Drop-Like 30 12.727
17
MCL002 Macular Corneal Dystrophy 54 10.392
18
FCL012 Facial Paralysis 53 10.392
19
P AMY082 Amyloidosis, Familial Visceral 48 10.392
20
c TYR013 Tyrosinemia, Type Ii 46 10.392
21
FCL011 Facial Nerve Disease 42 10.392
22
CRP017 Carpal Tunnel Syndrome, Familial 42 10.392
23
RHM008 Rheumatic Myocarditis 41 10.392
24
CHN008 Chandler Syndrome 38 10.392
25
c MYP082 Myopathy, Myofibrillar, 2 37 10.392
26
BLP001 Blepharochalasis 37 10.392
27
NRV004 Nerve Compression Syndrome 36 10.392
28
AMY005 Amyloid Neuropathy 33 10.392
29
CRN247 Corneal Dystrophy, Thiel-Behnke Type 32 10.392
30
RDL004 Radial Neuropathy 30 10.392
31
c CRN236 Corneal Dystrophy, Lattice Type I 30 10.392
32
c LTT008 Lattice Corneal Dystrophy Type Ii 22 10.392
33
EPT024 Epithelial-Stromal Tgfbi Dystrophy 13 10.392
34
AGL003 Agel Amyloidosis 17 7.348