Search results for tafamidis

88 hits were found for tafamidis

# Family MCID Name MIFTS Score
1
P AMY004 Amyloidosis 69 12.048
2
c ATR087 Atrial Standstill 1 74 10.225
3
P PLY019 Polyneuropathy 53 9.955
5
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 5.403
6
P HRD207 Hereditary Transthyretin Amyloidosis 25 5.229
7
DBT010 Diabetic Neuropathy 54 2.962
8
P TRN020 Turner Syndrome 67 2.482
9
AMY005 Amyloid Neuropathy 31 2.470
10
P NRP001 Neuropathy 59 2.066
11
ATN005 Autonomic Dysfunction 45 1.794
12
c HRD039 Hereditary Amyloidosis 45 1.626
13
P PRP019 Peripheral Nervous System Disease 57 1.567
14
ATN004 Autonomic Neuropathy 42 1.452
15
RHB024 Rhabdomyosarcoma 2 65 1.449
16
WLD005 Wild Type Attr Amyloidosis 29 1.315
17
P RST002 Restrictive Cardiomyopathy 54 1.292
18
TRN015 Transient Cerebral Ischemia 62 1.244
19
P DYS021 Dysautonomia 38 1.218
20
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.162
21
P URN019 Urinary Tract Infection 49 1.162
22
P DRR001 Diarrhea 55 1.162
23
MTR007 Motor Peripheral Neuropathy 41 1.162
24
P SDR002 Siderosis 42 1.162
25
SYN036 Syncope 44 1.097
26
CNG034 Congestive Heart Failure 69 1.060
27
P MLN008 Melanoma 75 1.060
28
P PNC035 Pancreatic Cancer 86 1.060
29
PRT058 Pure Autonomic Failure 58 1.060
30
PRT251 Proteinuria, Chronic Benign 58 1.049
31
P HRT032 Heart Disease 84 1.017
32
c ACT068 Acute Cystitis 61 0.966
33
MTR002 Mitral Valve Insufficiency 51 0.966
34
P CRP001 Carpal Tunnel Syndrome 66 0.449
35
c ALM001 Al Amyloidosis 54 0.420
36
P AXN001 Axonal Neuropathy 33 0.420
37
P HYP061 Hypertrophic Cardiomyopathy 69 0.355
38
KRT001 Keratoconjunctivitis Sicca 49 0.318
39
KRT006 Keratoconjunctivitis 53 0.318
40
ERY029 Erythermalgia, Primary 58 0.275
41
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 0.275
42
MYL069 Myeloma, Multiple 77 0.225
43
P CHR071 Charcot-Marie-Tooth Disease 64 0.225
44
PLS009 Plasma Cell Neoplasm 64 0.225
45
P DMY001 Demyelinating Polyneuropathy 41 0.225
46
IMP005 Impotence 52 0.225
47
TTH006 Tooth Disease 51 0.225
48
CNS004 Constipation 56 0.225
49
P ALZ034 Alzheimer Disease 87 0.159
50
c TYP009 Type 2 Diabetes Mellitus 92 0.159
51
RFS006 Refsum Disease, Classic 63 0.159
52
c BRN108 Branchiootic Syndrome 1 63 0.159
53
ANG054 Angina Pectoris 65 0.159
54
P BRW001 Brown-Vialetto-Van Laere Syndrome 50 0.159
55
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.159
56
P RHM011 Rheumatoid Arthritis 81 0.159
57
PLY023 Polycystic Liver Disease 62 0.159
58
P ATR011 Atrial Fibrillation 66 0.159
59
ATM095 Autoimmune Disease 61 0.159
60
PRP083 Porphyria, Acute Intermittent 64 0.159
61
P HRD021 Hereditary Sensory Neuropathy 48 0.159
62
ATR057 Atrioventricular Block 54 0.159
63
MNN017 Mononeuropathy 41 0.159
64
GT001 Gout 63 0.159
65
c INH020 Inherited Metabolic Disorder 47 0.159
66
ANH002 Anhidrosis 45 0.159
67
HYP014 Hyperuricemia 51 0.159
68
SNS003 Sensory Peripheral Neuropathy 51 0.159
69
P PRP029 Porphyria 60 0.159
70
P THR014 Thrombocytopenia 66 0.159
71
PMS001 Poems Syndrome 59 0.159
72
c DLT002 Dilated Cardiomyopathy 79 0.159
73
HYP006 Hypertensive Heart Disease 48 0.159
74
HMP001 Hemopericardium 47 0.159
75
P PRC012 Pericardial Effusion 50 0.159
76
P PLY020 Polyradiculoneuropathy 47 0.159
77
P ORT004 Orthostatic Intolerance 62 0.159
78
PHN003 Phenylketonuria 76 0.159
79
NRM005 Neuromuscular Disease 63 0.159
80
P MYP004 Myopathy 67 0.159
81
c HRD088 Hereditary Neuropathies 34 0.159
82
c AMY009 Amyloidosis Aa 47 0.159
83
P ART022 Arthritis 70 0.159
85
DST006 Diastolic Heart Failure 45 0.159
86
MLT075 Multifocal Motor Neuropathy 45 0.159
87
P PRM227 Primary Orthostatic Hypotension 23 0.159
88
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.159
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