Search results for Bepridil

124 hits were found for Bepridil

# Family MCID Name MIFTS Score
1
ANG054 Angina Pectoris 65 6.409
2
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 4.417
3
P ATR011 Atrial Fibrillation 66 4.079
4
ATR057 Atrioventricular Block 54 2.782
5
LPP008 Lipoprotein Quantitative Trait Locus 65 2.420
6
HYP005 Hypokalemia 55 2.245
7
P PNM007 Pneumonia 64 1.970
8
P SCK002 Sick Sinus Syndrome 55 1.932
9
P BRG001 Brugada Syndrome 69 1.751
10
INT007 Intermediate Coronary Syndrome 53 1.731
11
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.711
12
c HYP595 Hypertension, Essential 84 1.676
13
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.609
14
ILS001 Ileus 49 1.536
15
PRL008 Paralytic Ileus 44 1.536
16
P TRM003 Tremor 50 1.516
17
SNT005 Sinoatrial Node Disease 47 1.475
18
c LKM063 Leukemia, Chronic Myeloid 71 1.453
19
CRD223 Cardiac Arrhythmia 63 1.453
20
P MYL006 Myeloid Leukemia 60 1.453
21
P GLM040 Glioma Susceptibility 1 70 1.323
22
MLG169 Malignant Astrocytoma 57 1.323
23
P SCK005 Sickle Cell Disease 56 1.291
24
ANX004 Anoxia 40 1.256
25
SYN036 Syncope 44 1.256
26
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 57 1.216
27
CRB004 Cerebral Artery Occlusion 46 1.216
28
CRD132 Cardiac Conduction Defect 59 1.150
29
P HYP061 Hypertrophic Cardiomyopathy 69 1.125
30
P ATR081 Atrial Standstill 31 1.125
31
P HYP076 Hyperthyroidism 53 1.125
32
LPD008 Lipid Metabolism Disorder 61 1.100
33
48X005 48,xyyy 39 1.100
34
c ACT075 Acute Myocardial Infarction 55 1.100
35
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 1.072
36
P LKM071 Leukemia, Chronic Lymphocytic 74 1.072
37
P LKM002 Leukemia 66 1.072
38
WLF001 Wolff-Parkinson-White Syndrome 63 1.043
39
SVR001 Severe Acute Respiratory Syndrome 68 1.043
40
RST023 Resting Heart Rate, Variation in 40 1.043
41
THR099 Third-Degree Atrioventricular Block 42 1.011
42
ALL029 Allergic Disease 61 1.011
43
MRB001 Marburg Hemorrhagic Fever 40 1.011
44
END086 End Stage Renal Disease 54 1.011
45
P PLM037 Pulmonary Hypertension 69 0.976
46
TRY001 Trypanosomiasis 50 0.976
47
P KLZ004 Kala-Azar 1 41 0.976
48
c DLT002 Dilated Cardiomyopathy 79 0.976
49
CHG001 Chagas Disease 65 0.976
50
SYS003 Systolic Heart Failure 49 0.976
51
LSH001 Leishmaniasis 63 0.976
52
HYP056 Hypoglycemia 65 0.976
53
ANT024 Anthrax Disease 58 0.935
54
c ATR087 Atrial Standstill 1 74 0.888
55
ERL052 Early Repolarization Associated with Ventricular Fibrillation 21 0.826
56
P PLM036 Pulmonary Fibrosis 65 0.676
57
GRN017 Granulocytopenia 42 0.676
58
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.666
59
P LNG028 Long Qt Syndrome 63 0.474
60
P GRV001 Graves' Disease 54 0.367
61
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.335
62
GLB002 Glioblastoma 67 0.335
63
RGH001 Right Bundle Branch Block 47 0.335
64
P PRK039 Parkinsonism 55 0.300
65
SRC014 Sarcoma 64 0.300
66
SPN035 Spindle Cell Sarcoma 51 0.300
67
SFT003 Soft Tissue Sarcoma 57 0.300
68
ALL014 Allergic Encephalomyelitis 34 0.300
69
MLT131 Multifocal Atrial Tachycardia 17 0.300
70
CVD001 Covid-19 58 0.259
71
VLK001 Volkmann Contracture 22 0.259
72
GLM045 Glioma 62 0.259
73
GLL048 Glial Tumor 52 0.259
74
HYP266 Hypoxia 56 0.259
75
P MYP004 Myopathy 67 0.259
76
HLX001 Helix Syndrome 47 0.212
77
BCT022 Bacterial Infectious Disease 56 0.212
78
ALC007 Alcohol Dependence 65 0.212
79
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.212
80
P CRD119 Cardiac Arrest 68 0.212
81
FRS012 First-Degree Atrioventricular Block 39 0.212
82
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.212
83
RHM028 Rheumatic Heart Disease 56 0.212
84
CHL068 Cholestasis 61 0.212
85
ISC004 Ischemia 61 0.212
86
OCL022 Ocular Melanoma 54 0.212
87
DMY004 Demyelinating Disease 50 0.212
88
WLL004 Wallerian Degeneration 38 0.212
89
P NRB001 Neuroblastoma 66 0.212
90
HPT022 Hepatoblastoma 54 0.212
91
47X002 47,xyy 48 0.212
92
ART140 Arteries, Anomalies of 52 0.150
93
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.150
94
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.150
95
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.150
96
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.150
97
LFT001 Left Bundle Branch Hemiblock 47 0.150
98
IMM167 Immune Deficiency Disease 77 0.150
99
P SLP006 Sleep Apnea 69 0.150
100
LMB062 Limb Ischemia 55 0.150
101
c SHR030 Short Qt Syndrome 44 0.150
102
SLF016 Sulfonamide Allergy 23 0.150
103
HMN044 Human Immunodeficiency Virus Type 1 76 0.150
104
c DVL042 Developmental and Epileptic Encephalopathy 14 52 0.150
105
NRT004 Neuritis 53 0.150
106
ACT098 Acute Erythroid Leukemia 55 0.150
107
ACQ007 Acquired Immunodeficiency Syndrome 58 0.150
108
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.150
109
SQM006 Squamous Cell Carcinoma 59 0.150
110
SCH014 Schistosomiasis 56 0.150
111
P OPT009 Optic Neuritis 57 0.150
112
DPH001 Diphtheria 59 0.150
113
TTN003 Tetanus 64 0.150
114
OVR047 Ovarian Cystadenocarcinoma 38 0.150
115
HYP066 Hyperglycemia 60 0.150
116
TRN015 Transient Cerebral Ischemia 62 0.150
117
CYS014 Cystadenocarcinoma 51 0.150
118
SRS001 Serous Cystadenocarcinoma 51 0.150
119
CRN030 Coronary Stenosis 50 0.150
120
EBL001 Ebola Hemorrhagic Fever 56 0.150
121
MLG120 Malignant Migrating Partial Seizures of Infancy 44 0.150
122
P SZR006 Seizure Disorder 69 0.150
123
CRT015 Carotid Artery Occlusion 45 0.150
124
c FML294 Familial Short Qt Syndrome 44 0.150
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