Search results for "[genes] GSN"

31 hits were found for '[genes] GSN'

# Family MCID Name MIFTS Score
1
P AMY084 Amyloidosis, Finnish Type 42 24.593
2
P AMY004 Amyloidosis 65 20.973
3
P PLY019 Polyneuropathy 56 16.580
4
c HRD039 Hereditary Amyloidosis 46 16.580
5
CRN025 Corneal Dystrophy 42 16.580
6
P LTT001 Lattice Corneal Dystrophy 33 16.580
7
c FML249 Familial Amyloidosis, Finnish Type 19 16.580
8
CYS001 Cystic Fibrosis 83 14.830
9
P CRB019 Cerebral Amyloid Angiopathy 58 14.830
10
TCK001 Tick-Borne Encephalitis 50 14.830
11
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 14.830
12
CRN024 Corneal Disease 44 14.830
13
P CRN276 Corneal Endothelial Dystrophy 37 14.830
14
CRN106 Corneal Dystrophy, Gelatinous Drop-Like 31 14.830
15
INC002 Inclusion Body Myositis 66 12.843
16
FCL012 Facial Paralysis 50 12.843
17
P AMY082 Amyloidosis, Familial Visceral 45 12.843
18
c MYP082 Myopathy, Myofibrillar, 2 39 12.843
19
FCL011 Facial Nerve Disease 36 12.843
20
PDT025 Pediatric Multiple Sclerosis 36 12.843
21
RHM008 Rheumatic Myocarditis 35 12.843
22
BLP001 Blepharochalasis 34 12.843
23
AMY005 Amyloid Neuropathy 33 12.843
24
CLC057 Cole-Carpenter Syndrome 33 12.843
25
CRN247 Corneal Dystrophy, Thiel-Behnke Type 32 12.843
26
c CRN236 Corneal Dystrophy, Lattice Type I 28 12.843
27
RDL004 Radial Neuropathy 26 12.843
28
c LTT008 Lattice Corneal Dystrophy Type Ii 22 12.843
29
EPT024 Epithelial-Stromal Tgfbi Dystrophy 13 12.843
30
c TYR013 Tyrosinemia, Type Ii 46 10.486
31
P RTN008 Retinitis Pigmentosa 80 7.415