Search results for Amiloride hydrochloride

243 hits were found for Amiloride hydrochloride

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.360
2
ADL002 Adult Syndrome 69 0.311
3
c RHB024 Rhabdomyosarcoma 2 65 0.296
4
P ADN016 Adenocarcinoma 64 0.257
5
HYP005 Hypokalemia 55 0.245
6
48X005 48,xyyy 39 0.233
7
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.231
8
CYS001 Cystic Fibrosis 80 0.231
9
P KDN018 Kidney Disease 70 0.221
10
P LNG032 Lung Cancer 97 0.221
11
DPR016 Depression 63 0.201
12
MNT002 Mental Depression 57 0.199
13
CNG034 Congestive Heart Failure 70 0.198
14
P PNC035 Pancreatic Cancer 84 0.197
15
P CLR023 Colorectal Cancer 98 0.195
16
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.194
17
P GLM045 Glioma 63 0.177
18
GLL048 Glial Tumor 45 0.177
19
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.173
20
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.170
21
c CHR684 Chronic Kidney Disease 66 0.170
22
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.169
23
c PRM038 Primary Agammaglobulinemia 43 0.167
24
ANX010 Anxiety 72 0.162
25
CRB039 Cerebrovascular Disease 69 0.154
26
ALL026 Allergic Hypersensitivity Disease 64 0.153
27
ISC004 Ischemia 60 0.151
28
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.149
29
P OVR042 Ovarian Cancer 89 0.149
30
GLB015 Glioblastoma Multiforme 75 0.149
31
P SZR006 Seizure Disorder 58 0.147
32
HMN044 Human Immunodeficiency Virus Type 1 71 0.147
33
LVR012 Liver Cirrhosis 63 0.145
34
P CRD246 Cardiovascular System Disease 56 0.145
35
P DBT009 Diabetes Mellitus 64 0.144
36
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.143
37
P NRB001 Neuroblastoma 71 0.143
38
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.142
39
P HRT032 Heart Disease 75 0.141
40
c MLG068 Malignant Glioma 45 0.140
41
P CHR345 Chronic Pain 50 0.137
42
STR067 Stroke, Ischemic 80 0.137
43
VSL002 Visual Epilepsy 58 0.136
44
ANG054 Angina Pectoris 66 0.136
45
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.135
46
NTR005 Nutritional Deficiency Disease 61 0.134
47
LNG099 Lung Disease 61 0.134
48
P MYC007 Myocardial Infarction 70 0.131
49
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.130
50
P NRP001 Neuropathy 56 0.130
51
49X006 49, Xxxxy Syndrome 41 0.128
52
P DBT005 Diabetes Insipidus 55 0.128
53
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.128
54
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.128
55
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.128
56
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.128
57
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.128
58
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.128
59
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.128
60
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.128
61
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.128
62
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.128
63
DRM006 Dermatitis 61 0.126
64
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.126
65
END030 End Stage Renal Failure 58 0.126
66
MTB004 Metabolic Acidosis 50 0.126
67
TRN018 Transitional Cell Carcinoma 56 0.125
68
P HYP069 Hyperparathyroidism 62 0.125
69
P MLT020 Multiple Sclerosis 72 0.123
70
ERY051 Erythroleukemia, Familial 56 0.121
71
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.121
72
PLM010 Pulmonary Edema 55 0.119
73
HYP066 Hyperglycemia 61 0.118
74
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.118
75
MYL069 Myeloma, Multiple 85 0.116
76
ATX019 Ataxia with Vitamin E Deficiency 48 0.115
77
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.115
78
c MGR028 Migraine with or Without Aura 1 69 0.115
79
47X002 47,xyy 49 0.114
80
P AST007 Astrocytoma 50 0.113
81
PRT037 Pertussis 65 0.112
82
ADN018 Adenoma 58 0.112
83
ESP021 Esophageal Cancer 90 0.111
84
P GST053 Gastric Cancer 83 0.111
85
CLN015 Colon Adenocarcinoma 63 0.110
86
HYP266 Hypoxia 56 0.110
87
P EXN002 Exanthem 57 0.110
88
c LKM063 Leukemia, Chronic Myeloid 71 0.107
89
SPN186 Spinal Cord Injury 60 0.106
90
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.106
91
P CRN300 Coronary Heart Disease 1 63 0.105
92
c MCR120 Microvascular Complications of Diabetes 7 47 0.105
93
P CRN018 Coronary Artery Anomaly 63 0.103
94
P ATR011 Atrial Fibrillation 66 0.102
95
P CRD119 Cardiac Arrest 67 0.102
96
P NPH012 Nephrotic Syndrome 63 0.101
97
BRN024 Bronchitis 68 0.101
98
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.100
99
OST159 Osteogenic Sarcoma 66 0.100
100
P LVR013 Liver Disease 68 0.099
101
P HDC001 Headache 57 0.099
102
c MCR113 Microvascular Complications of Diabetes 3 52 0.098
103
c MCR130 Microvascular Complications of Diabetes 6 41 0.098
104
c MCR133 Microvascular Complications of Diabetes 4 41 0.098
105
P PNC025 Panic Disorder 53 0.098
106
P HYP086 Hypothyroidism 68 0.097
107
MSC007 Muscle Hypertrophy 63 0.096
108
CNT047 Contact Dermatitis 57 0.096
109
P PLM037 Pulmonary Hypertension 68 0.095
110
INT007 Intermediate Coronary Syndrome 55 0.094
111
ART140 Arteries, Anomalies of 53 0.094
112
ATH013 Atherosclerosis Susceptibility 66 0.094
113
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.093
114
c MCR129 Microvascular Complications of Diabetes 1 66 0.092
115
P MCR115 Microvascular Complications of Diabetes 5 66 0.091
116
STT001 Status Epilepticus 59 0.091
117
IMP005 Impotence 52 0.091
118
BRN071 Brain Injury 49 0.090
119
P MDL005 Medulloblastoma 77 0.090
120
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.088
121
P OPT006 Optic Nerve Disease 57 0.086
122
CYT002 Cytokine Deficiency 44 0.086
123
P OPT009 Optic Neuritis 56 0.086
124
NRT004 Neuritis 53 0.086
125
BNR002 Bone Resorption Disease 48 0.085
126
c FNC043 Fanconi Anemia, Complementation Group E 62 0.085
127
P ENC018 Encephalopathy 61 0.084
128
CMM005 Common Cold 56 0.084
129
P FBR017 Fibrosarcoma 56 0.083
130
GLC003 Glucose Intolerance 54 0.083
131
TRM010 Traumatic Brain Injury 53 0.082
132
P VSC007 Vascular Disease 63 0.081
133
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.081
134
P EPL164 Epilepsy 71 0.079
135
c FML035 Familial Hyperlipidemia 55 0.079
136
IRN002 Iron Metabolism Disease 57 0.078
137
ALL010 Allergic Contact Dermatitis 55 0.078
138
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.078
139
ILS001 Ileus 51 0.077
140
P RNL007 Renal Tubular Acidosis 50 0.076
141
P SLP006 Sleep Apnea 69 0.076
142
c FML001 Familial Atrial Fibrillation 66 0.076
143
ATR057 Atrioventricular Block 55 0.076
144
P INF038 Influenza 68 0.075
145
HYP056 Hypoglycemia 66 0.075
146
LPD008 Lipid Metabolism Disorder 62 0.075
147
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.074
148
CHL014 Cholera 55 0.074
149
c HPT001 Hepatitis C 63 0.074
150
AGN016 Aging 56 0.074
151
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.073
152
P CTR002 Cataract 60 0.072
153
SCL003 Social Phobia 48 0.072
154
P PHC003 Pheochromocytoma 71 0.071
155
P PNM007 Pneumonia 68 0.071
156
P BND020 Bone Disease 59 0.071
157
ADR040 Adrenal Gland Pheochromocytoma 46 0.071
158
c ACT075 Acute Myocardial Infarction 56 0.071
159
P PLY018 Polycythemia 55 0.070
160
SNS003 Sensory Peripheral Neuropathy 53 0.069
161
CRB004 Cerebral Artery Occlusion 44 0.069
162
c ATR087 Atrial Standstill 1 74 0.069
163
GNR004 Generalized Anxiety Disorder 56 0.069
164
PPL001 Papillary Adenoma 45 0.069
165
DMY004 Demyelinating Disease 52 0.068
166
HYP540 Hypertension, Diastolic 40 0.068
167
RCK004 Rickets 69 0.067
168
P BRS044 Breast Adenocarcinoma 59 0.067
169
GST023 Gastric Ulcer 53 0.067
170
MCN017 Meconium Ileus 52 0.067
171
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.067
172
P CYS018 Cystitis 59 0.066
173
APN008 Apnea, Obstructive Sleep 65 0.065
174
c PRM005 Primary Hyperparathyroidism 58 0.065
175
c MCR112 Microvascular Complications of Diabetes 2 41 0.065
176
P OCL013 Oculodentodigital Dysplasia 69 0.064
177
c HPT073 Hepatitis C Virus 70 0.063
178
RHM027 Rheumatic Disease 56 0.063
179
HYP081 Hypolipoproteinemia 50 0.063
180
FBR012 Fabry Disease 71 0.063
181
c PRC016 Pre-Eclampsia 63 0.062
182
c ACT071 Acute Kidney Failure 59 0.062
183
HLX001 Helix Syndrome 47 0.062
184
ANX004 Anoxia 42 0.062
185
GST092 Gastroesophageal Reflux 65 0.061
186
BRN004 Brain Edema 55 0.061
187
MCL006 Macular Retinal Edema 55 0.060
188
P PLY014 Polycystic Kidney Disease 59 0.059
189
PPT005 Peptic Ulcer Disease 58 0.058
190
PRT036 Peritonitis 65 0.056
191
URN010 Urinary Tract Obstruction 57 0.056
193
HPT019 Hepatic Encephalopathy 60 0.054
194
P LCT001 Lactic Acidosis 51 0.054
195
CCN001 Cocaine Dependence 48 0.054
196
HPT004 Hepatic Coma 43 0.054
197
CNN003 Conn's Syndrome 79 0.053
198
SPP011 Suppression of Tumorigenicity 12 59 0.053
199
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.053
200
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.053
201
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.053
202
c DLT002 Dilated Cardiomyopathy 79 0.052
203
SYN007 Synovitis 55 0.052
204
P INT143 Interstitial Cystitis 61 0.050
205
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.050
206
P GLM007 Glomerulonephritis 57 0.050
207
P MSC003 Muscular Atrophy 52 0.050
208
NPH003 Nephrocalcinosis 51 0.048
209
HYP014 Hyperuricemia 51 0.048
210
CRN019 Coronary Artery Vasospasm 46 0.048
211
CRT015 Carotid Artery Occlusion 44 0.048
212
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.048
213
NRM005 Neuromuscular Disease 63 0.048
214
GST045 Gastroenteritis 59 0.048
215
CRD132 Cardiac Conduction Defect 59 0.048
216
P HYP024 Hypoparathyroidism 55 0.048
217
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.045
218
INS001 Insulinoma 60 0.045
219
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.045
220
P HYP076 Hyperthyroidism 55 0.045
221
SPL018 Splenomegaly 48 0.045
222
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.045
223
AGR002 Agoraphobia 44 0.045
224
P MYC008 Myocarditis 59 0.042
225
MNR012 Meniere Disease 57 0.042
226
MTH009 Mouth Disease 56 0.042
227
P TMP001 Temporal Lobe Epilepsy 50 0.042
228
INP001 Inappropriate Adh Syndrome 49 0.042
229
DBT006 Diabetic Macular Edema 48 0.042
230
ATS010 Autosomal Recessive Disease 48 0.042
231
CRN027 Corneal Neovascularization 47 0.042
232
URT010 Ureteral Obstruction 46 0.042
233
c PCH010 Pachyonychia Congenita 3 43 0.042
234
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.042
235
ADR057 Adrenogenital Syndrome 32 0.042
236
ADG002 Audiogenic Seizures 26 0.042
237
P SPN046 Spinal Muscular Atrophy 64 0.037
238
PRT013 Portal Hypertension 60 0.037
239
HYD002 Hydronephrosis 59 0.037
240
c SPN393 Spinal Muscular Atrophy, Type I 53 0.037
241
c PRM108 Primary Progressive Multiple Sclerosis 51 0.037
242
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.037
243
OBS082 Obstructive Nephropathy 43 0.037
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