Search results for "[genes] TTR"

72 hits were found for '[genes] TTR'

# Family MCID Name MIFTS Score
1
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 20.791
2
P AMY004 Amyloidosis 64 18.596
3
HYP029 Hyperthyroxinemia 25 16.104
4
P RSP003 Respiratory Failure 70 14.701
5
P CRD011 Cardiomyopathy 67 14.701
6
P PLY019 Polyneuropathy 54 14.701
7
CRP017 Carpal Tunnel Syndrome, Familial 44 14.701
8
NTR005 Nutritional Deficiency Disease 39 14.701
9
PHN003 Phenylketonuria 73 13.149
10
c CHR089 Chronic Kidney Failure 66 13.149
11
P CRB019 Cerebral Amyloid Angiopathy 58 13.149
12
P RST002 Restrictive Cardiomyopathy 50 13.149
13
PRT038 Protein-Energy Malnutrition 49 13.149
14
OBS001 Obstructive Jaundice 48 13.149
15
c HRD039 Hereditary Amyloidosis 44 13.149
16
P CHR573 Choroid Plexus Cancer 43 13.149
17
HYP645 Hyperthyroxinemia, Dystransthyretinemic 16 13.149
18
LPT007 Leptomeningeal Amyloidosis 13 13.149
19
P ALZ034 Alzheimer Disease 93 11.388
20
CHR029 Choroid Plexus Papilloma 55 11.388
21
KRT002 Keratomalacia 54 11.388
22
SHG001 Shigellosis 53 11.388
23
NRM002 Normal Pressure Hydrocephalus 50 11.388
24
P AMY082 Amyloidosis, Familial Visceral 46 11.388
25
DCB001 Decubitus Ulcer 44 11.388
26
GLS007 Glossitis 44 11.388
27
P DMY001 Demyelinating Polyneuropathy 43 11.388
28
DYS015 Dysentery 41 11.388
29
c HYP058 Hypervitaminosis a 38 11.388
30
AMY005 Amyloid Neuropathy 32 11.388
31
FML097 Familial Amyloid Cardiomyopathy 17 11.388
32
c CNT035 Central Nervous System Disease 59 9.298
33
P PRP019 Peripheral Nervous System Disease 54 9.298
34
BRT005 Barth Syndrome 53 9.298
35
BRN106 Burns 52 9.298
36
PRT058 Pure Autonomic Failure 51 9.298
37
ATN002 Autonomic Nervous System Disease 47 9.298
38
P ANL018 Analbuminemia 46 9.298
39
KWS001 Kwashiorkor 44 9.298
40
P AMY084 Amyloidosis, Finnish Type 43 9.298
41
MNN020 Meningococcal Infection 43 9.298
42
CHR100 Chronic Ulcer of Skin 42 9.298
43
TST018 Testicular Yolk Sac Tumor 42 9.298
44
c CHR096 Chronic Pulmonary Heart Disease 40 9.298
45
MLY001 Molybdenum Cofactor Deficiency 40 9.298
46
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 39 9.298
47
MRS001 Marasmus 39 9.298
48
c AMY009 Amyloidosis Aa 39 9.298
49
LCL004 Localized Osteosarcoma 38 9.298
50
AMY002 Amyloid Tumor 37 9.298
51
BLD009 Bladder Neck Obstruction 36 9.298
52
BLP001 Blepharochalasis 36 9.298
53
NRV004 Nerve Compression Syndrome 35 9.298
54
PDT025 Pediatric Multiple Sclerosis 35 9.298
55
BRW004 Brown-Sequard Syndrome 32 9.298
56
PPL013 Papillary Ependymoma 32 9.298
57
ATR073 Atrophic Glossitis 31 9.298
58
TRS001 Tarsal Tunnel Syndrome 29 9.298
59
HYP047 Hypertropia 28 9.298
60
MDN001 Median Rhomboid Glossitis 28 9.298
61
LGN005 Ligneous Conjunctivitis 28 9.298
62
TBL007 Tibial Neuropathy 28 9.298
63
CRT011 Carotenemia 25 9.298
64
TBR007 Tuberculum Sellae Meningioma 23 9.298
65
P DYS070 Dysalbuminemic Hyperthyroxinemia 20 9.298
66
ATN001 Autonomic Peripheral Neuropathy 20 9.298
67
SLL002 Sella Turcica Neoplasm 18 9.298
68
PRM123 Paramyloidosis 16 9.298
69
FML141 Familial Oculoleptomeningeal Amyloidosis 8 9.298
70
P NRV007 Nervous System Disease 71 6.575
71
ATR060 Atrial Standstill, Digenic 53 6.575
72
P ACQ009 Acquired Metabolic Disease 41 6.575