Search results for "[genes] TTR"

76 hits were found for '[genes] TTR'

# Family MCID Name MIFTS Score
1
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 21.681
2
P AMY004 Amyloidosis 65 18.489
3
P RSP003 Respiratory Failure 71 16.012
4
P PLY019 Polyneuropathy 56 16.012
5
CRP017 Carpal Tunnel Syndrome, Familial 43 16.012
6
NTR005 Nutritional Deficiency Disease 36 16.012
7
HYP029 Hyperthyroxinemia 26 16.012
8
PHN003 Phenylketonuria 72 14.617
9
P CRD011 Cardiomyopathy 68 14.617
10
c CHR089 Chronic Kidney Failure 66 14.617
11
P CRB019 Cerebral Amyloid Angiopathy 58 14.617
12
P RST002 Restrictive Cardiomyopathy 50 14.617
13
PRT038 Protein-Energy Malnutrition 49 14.617
14
OBS001 Obstructive Jaundice 48 14.617
15
c HRD039 Hereditary Amyloidosis 46 14.617
16
P CHR573 Choroid Plexus Cancer 41 14.617
17
P ALZ034 Alzheimer Disease 92 13.074
18
CHR029 Choroid Plexus Papilloma 55 13.074
19
SHG001 Shigellosis 54 13.074
20
P EPN002 Ependymoma 53 13.074
21
KRT002 Keratomalacia 52 13.074
22
NRM002 Normal Pressure Hydrocephalus 50 13.074
23
P AMY082 Amyloidosis, Familial Visceral 45 13.074
24
GLS007 Glossitis 44 13.074
25
P DMY001 Demyelinating Polyneuropathy 43 13.074
26
DCB001 Decubitus Ulcer 41 13.074
27
DYS015 Dysentery 40 13.074
28
c HYP058 Hypervitaminosis a 39 13.074
29
AMY005 Amyloid Neuropathy 33 13.074
30
FML097 Familial Amyloid Cardiomyopathy 17 13.074
31
HYP645 Hyperthyroxinemia, Dystransthyretinemic 15 13.074
32
LPT007 Leptomeningeal Amyloidosis 13 13.074
33
c CNT035 Central Nervous System Disease 60 11.322
34
PRP019 Peripheral Nervous System Disease 55 11.322
35
BRT005 Barth Syndrome 52 11.322
36
BRN106 Burns 52 11.322
37
PRT058 Pure Autonomic Failure 52 11.322
38
ATR060 Atrial Standstill, Digenic 51 11.322
39
ATN002 Autonomic Nervous System Disease 48 11.322
40
P ANL018 Analbuminemia 44 11.322
41
MNN020 Meningococcal Infection 43 11.322
42
P AMY084 Amyloidosis, Finnish Type 42 11.322
43
KWS001 Kwashiorkor 40 11.322
44
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 40 11.322
45
c CHR096 Chronic Pulmonary Heart Disease 40 11.322
46
TST018 Testicular Yolk Sac Tumor 40 11.322
47
CHR100 Chronic Ulcer of Skin 40 11.322
48
c AMY009 Amyloidosis Aa 39 11.322
49
MLY001 Molybdenum Cofactor Deficiency 38 11.322
50
AMY002 Amyloid Tumor 37 11.322
51
MRS001 Marasmus 36 11.322
52
PDT025 Pediatric Multiple Sclerosis 36 11.322
53
LCL004 Localized Osteosarcoma 35 11.322
54
BLD009 Bladder Neck Obstruction 35 11.322
55
LGN005 Ligneous Conjunctivitis 34 11.322
56
BLP001 Blepharochalasis 34 11.322
57
PPL013 Papillary Ependymoma 31 11.322
58
TRS001 Tarsal Tunnel Syndrome 31 11.322
59
NRV004 Nerve Compression Syndrome 31 11.322
60
ATR073 Atrophic Glossitis 30 11.322
61
BRW004 Brown-Sequard Syndrome 29 11.322
62
MDN001 Median Rhomboid Glossitis 29 11.322
63
HYP047 Hypertropia 28 11.322
64
TBL007 Tibial Neuropathy 28 11.322
65
TBR007 Tuberculum Sellae Meningioma 24 11.322
66
CRT011 Carotenemia 23 11.322
67
ATN001 Autonomic Peripheral Neuropathy 17 11.322
68
PRM123 Paramyloidosis 17 11.322
69
SLL002 Sella Turcica Neoplasm 17 11.322
70
P DYS070 Dysalbuminemic Hyperthyroxinemia 16 11.322
71
FML141 Familial Oculoleptomeningeal Amyloidosis 8 11.322
72
P NRV007 Nervous System Disease 71 9.245
73
P ACQ009 Acquired Metabolic Disease 38 9.245
74
RTN175 Retinitis Pigmentosa 7 and Digenic 38 9.245
75
P ATR081 Atrial Standstill 37 9.245
76
ALT002 Aleutian Mink Disease 33 9.245