Search results for "[genes] TTR"

33 hits were found for '[genes] TTR'

# Family MCID Name MIFTS Score
1
AMY087 Amyloidosis, Hereditary, Transthyretin-Related 33 64.637
2
P AMY004 Amyloidosis 63 20.700
3
P PLY019 Polyneuropathy 52 17.927
4
LVR012 Liver Cirrhosis 66 14.637
5
CHR029 Choroid Plexus Papilloma 61 14.637
6
P CRB019 Cerebral Amyloid Angiopathy 59 14.637
7
MLY001 Molybdenum Cofactor Deficiency 45 14.637
8
PRT038 Protein-Energy Malnutrition 40 14.637
9
HYP029 Hyperthyroxinemia 36 14.637
10
CRP017 Carpal Tunnel Syndrome, Familial 29 12.676
11
HYP645 Hyperthyroxinemia, Dystransthyretinemic 11 12.676
12
TRN064 Transthyretin-Related Familial Amyloid Cardiomyopathy 11 12.676
13
TKY001 Takayasu's Arteritis 60 10.350
14
BRT005 Barth Syndrome 58 10.350
15
c ALM001 Al Amyloidosis 56 10.350
16
P FND001 Fundus Albipunctatus 52 10.350
17
P SDR002 Siderosis 49 10.350
18
P RST002 Restrictive Cardiomyopathy 45 10.350
19
GLS007 Glossitis 43 10.350
20
OBS001 Obstructive Jaundice 42 10.350
21
c HRD039 Hereditary Amyloidosis 41 10.350
22
P HYP058 Hypervitaminosis a 41 10.350
23
SPR066 Superficial Siderosis 33 10.350
24
P AMY084 Amyloidosis, Finnish Type 32 10.350
25
c FML249 Familial Amyloidosis, Finnish Type 31 10.350
26
PRS063 Paresthesia 31 10.350
27
DYS070 Dysalbuminemic Hyperthyroxinemia 27 10.350
28
SNL010 Senile Systemic Amyloidosis 24 10.350
29
AMY005 Amyloid Neuropathy 23 10.350
30
ATR073 Atrophic Glossitis 18 10.350
31
FML097 Familial Amyloid Cardiomyopathy 14 10.350
32
LPT007 Leptomeningeal Amyloidosis 10 10.350
33
FML141 Familial Oculoleptomeningeal Amyloidosis 8 10.350