Search results for "[genes] TTR"

72 hits were found for '[genes] TTR'

# Family MCID Name MIFTS Score
1
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 49 19.839
2
P AMY004 Amyloidosis 68 18.704
3
HYP029 Hyperthyroxinemia 28 16.198
4
P PLY019 Polyneuropathy 55 14.787
5
NTR005 Nutritional Deficiency Disease 54 14.787
6
CRP017 Carpal Tunnel Syndrome, Familial 42 14.787
7
PHN003 Phenylketonuria 72 13.226
8
P CRD011 Cardiomyopathy 68 13.226
9
P CRB019 Cerebral Amyloid Angiopathy 56 13.226
10
OBS001 Obstructive Jaundice 51 13.226
11
PRT038 Protein-Energy Malnutrition 50 13.226
12
c HRD039 Hereditary Amyloidosis 49 13.226
13
P RST002 Restrictive Cardiomyopathy 48 13.226
14
P CHR573 Choroid Plexus Cancer 44 13.226
15
LPT007 Leptomeningeal Amyloidosis 16 13.226
16
HYP645 Hyperthyroxinemia, Dystransthyretinemic 13 13.226
17
P ALZ034 Alzheimer Disease 94 11.454
18
KRT002 Keratomalacia 58 11.454
19
SHG001 Shigellosis 57 11.454
20
P DRR001 Diarrhea 56 11.454
21
P EPN002 Ependymoma 53 11.454
22
CHR029 Choroid Plexus Papilloma 52 11.454
23
DCB001 Decubitus Ulcer 51 11.454
24
GLS007 Glossitis 50 11.454
25
P AMY082 Amyloidosis, Familial Visceral 48 11.454
26
P DMY001 Demyelinating Polyneuropathy 41 11.454
27
c HYP058 Hypervitaminosis a 36 11.454
28
AMY005 Amyloid Neuropathy 33 11.454
29
c CNT035 Central Nervous System Disease 61 9.352
30
c ALM001 Al Amyloidosis 56 9.352
31
PRT058 Pure Autonomic Failure 54 9.352
32
P FND001 Fundus Albipunctatus 53 9.352
33
BRT005 Barth Syndrome 50 9.352
34
BRN106 Burns 48 9.352
35
PRS063 Paresthesia 47 9.352
36
PRP019 Peripheral Nervous System Disease 46 9.352
37
ATN002 Autonomic Nervous System Disease 46 9.352
38
BLD009 Bladder Neck Obstruction 47 9.352
39
MNN020 Meningococcal Infection 45 9.352
40
KWS001 Kwashiorkor 45 9.352
41
CHR100 Chronic Ulcer of Skin 45 9.352
42
P ACQ009 Acquired Metabolic Disease 43 9.352
43
ATR073 Atrophic Glossitis 43 9.352
44
MLY001 Molybdenum Cofactor Deficiency 41 9.352
45
XRP001 Xerophthalmia 41 9.352
46
LCL004 Localized Osteosarcoma 41 9.352
47
TST018 Testicular Yolk Sac Tumor 40 9.352
48
c AMY009 Amyloidosis Aa 39 9.352
49
AMY002 Amyloid Tumor 39 9.352
50
MRS001 Marasmus 39 9.352
51
P AMY084 Amyloidosis, Finnish Type 38 9.352
52
BLP001 Blepharochalasis 37 9.352
53
NRV004 Nerve Compression Syndrome 36 9.352
54
HYP047 Hypertropia 35 9.352
55
TRS001 Tarsal Tunnel Syndrome 33 9.352
56
BRW004 Brown-Sequard Syndrome 33 9.352
57
LGN005 Ligneous Conjunctivitis 32 9.352
58
PPL013 Papillary Ependymoma 32 9.352
59
TBL007 Tibial Neuropathy 30 9.352
60
MDN001 Median Rhomboid Glossitis 28 9.352
61
TBR007 Tuberculum Sellae Meningioma 27 9.352
62
CRT011 Carotenemia 26 9.352
63
P DYS070 Dysalbuminemic Hyperthyroxinemia 24 9.352
64
ATN001 Autonomic Peripheral Neuropathy 23 9.352
65
FML097 Familial Amyloid Cardiomyopathy 22 9.352
66
SLL002 Sella Turcica Neoplasm 21 9.352
67
CNJ011 Conjunctival Deposit 20 9.352
68
PRM123 Paramyloidosis 16 9.352
69
FML141 Familial Oculoleptomeningeal Amyloidosis 11 9.352
70
P NRV007 Nervous System Disease 70 6.613
71
ATT014 Attrv30m Amyloidosis 12 6.613
72
ATT015 Attrv122i Amyloidosis 12 6.613