Search results for "[genes] GSN"

30 hits were found for '[genes] GSN'

# Family MCID Name MIFTS Score
1
P AMY084 Amyloidosis, Finnish Type 43 23.499
2
P AMY004 Amyloidosis 64 21.018
3
P PLY019 Polyneuropathy 54 16.616
4
CRN025 Corneal Dystrophy 41 16.616
5
P LTT001 Lattice Corneal Dystrophy 32 16.616
6
c FML249 Familial Amyloidosis, Finnish Type 17 16.616
7
BLD087 Bladder Cancer, Somatic 67 14.862
8
c HRD039 Hereditary Amyloidosis 44 14.862
9
CYS001 Cystic Fibrosis 86 12.871
10
P CRB019 Cerebral Amyloid Angiopathy 58 12.871
11
TCK001 Tick-Borne Encephalitis 49 12.871
12
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 12.871
13
CRN024 Corneal Disease 44 12.871
14
P CRN276 Corneal Endothelial Dystrophy 38 12.871
15
CRN106 Corneal Dystrophy, Gelatinous Drop-Like 29 12.871
16
c LTT008 Lattice Corneal Dystrophy Type Ii 23 12.871
17
INC002 Inclusion Body Myositis 63 10.509
18
FCL012 Facial Paralysis 50 10.509
19
P AMY082 Amyloidosis, Familial Visceral 46 10.509
20
FCL011 Facial Nerve Disease 38 10.509
21
c MYP082 Myopathy, Myofibrillar, 2 37 10.509
22
RHM008 Rheumatic Myocarditis 36 10.509
23
BLP001 Blepharochalasis 36 10.509
24
PDT025 Pediatric Multiple Sclerosis 35 10.509
25
CRN247 Corneal Dystrophy, Thiel-Behnke Type 32 10.509
26
AMY005 Amyloid Neuropathy 32 10.509
27
CLC057 Cole-Carpenter Syndrome 30 10.509
28
c CRN236 Corneal Dystrophy, Lattice Type I 29 10.509
29
RDL004 Radial Neuropathy 27 10.509
30
EPT024 Epithelial-Stromal Tgfbi Dystrophy 12 10.509