Search results for Amiloride hydrochloride

244 hits were found for Amiloride hydrochloride

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.354
2
ADL002 Adult Syndrome 70 0.282
3
P ADN016 Adenocarcinoma 64 0.253
4
HYP005 Hypokalemia 55 0.244
5
CYS001 Cystic Fibrosis 81 0.228
6
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.225
7
P LNG032 Lung Cancer 98 0.219
8
P KDN018 Kidney Disease 72 0.218
9
48X005 48,xyyy 39 0.214
10
DPR016 Depression 63 0.195
11
CNG034 Congestive Heart Failure 69 0.194
12
MNT002 Mental Depression 58 0.194
13
P CLR023 Colorectal Cancer 99 0.193
14
P PNC035 Pancreatic Cancer 84 0.192
15
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.190
16
P GLM045 Glioma 63 0.173
17
GLL048 Glial Tumor 45 0.173
18
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.171
19
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.169
20
c PRM038 Primary Agammaglobulinemia 44 0.168
21
c CHR684 Chronic Kidney Disease 70 0.164
22
ANX010 Anxiety 73 0.160
23
ISC004 Ischemia 58 0.159
24
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.150
25
P OVR042 Ovarian Cancer 88 0.147
26
CRB039 Cerebrovascular Disease 67 0.147
27
P SZR006 Seizure Disorder 56 0.146
28
GLB015 Glioblastoma Multiforme 75 0.146
29
P HRT032 Heart Disease 75 0.144
30
P CRD246 Cardiovascular System Disease 57 0.144
31
HMN044 Human Immunodeficiency Virus Type 1 71 0.143
32
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.143
33
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.142
34
P NRB001 Neuroblastoma 72 0.141
35
LVR012 Liver Cirrhosis 62 0.139
36
P DBT009 Diabetes Mellitus 64 0.139
37
c MLG068 Malignant Glioma 46 0.136
38
ANG054 Angina Pectoris 66 0.135
39
P CHR345 Chronic Pain 44 0.135
40
VSL002 Visual Epilepsy 59 0.135
41
STR067 Stroke, Ischemic 81 0.135
42
LNG099 Lung Disease 60 0.133
43
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.132
44
P MYC007 Myocardial Infarction 70 0.132
45
NTR005 Nutritional Deficiency Disease 62 0.132
46
P NRP001 Neuropathy 56 0.128
47
P DBT005 Diabetes Insipidus 55 0.126
48
49X006 49, Xxxxy Syndrome 41 0.125
49
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.125
50
DRM006 Dermatitis 61 0.124
51
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.123
52
TRN018 Transitional Cell Carcinoma 56 0.123
53
MTB004 Metabolic Acidosis 50 0.123
54
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.123
55
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.123
56
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.123
57
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.123
58
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.123
59
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.123
60
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.123
61
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.123
62
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.123
63
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.123
64
P HYP069 Hyperparathyroidism 63 0.122
65
P MLT020 Multiple Sclerosis 72 0.121
66
ERY051 Erythroleukemia, Familial 56 0.118
67
HYP066 Hyperglycemia 61 0.117
68
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.116
69
PLM010 Pulmonary Edema 54 0.116
70
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.116
71
ALL026 Allergic Hypersensitivity Disease 62 0.116
72
MYL069 Myeloma, Multiple 85 0.114
73
END086 End Stage Renal Disease 51 0.114
74
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.114
75
47X002 47,xyy 49 0.112
76
ATX019 Ataxia with Vitamin E Deficiency 42 0.111
77
P AST007 Astrocytoma 51 0.110
78
PRT037 Pertussis 65 0.110
79
ADN018 Adenoma 59 0.109
80
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.109
81
P GST053 Gastric Cancer 83 0.109
82
HYP266 Hypoxia 57 0.109
83
ESP021 Esophageal Cancer 90 0.108
84
P EXN002 Exanthem 57 0.108
85
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.108
86
CLN015 Colon Adenocarcinoma 65 0.108
87
c MGR028 Migraine with or Without Aura 1 67 0.106
88
SPN186 Spinal Cord Injury 60 0.103
89
c MCR120 Microvascular Complications of Diabetes 7 47 0.103
90
P CRN300 Coronary Heart Disease 1 63 0.102
91
P CRD119 Cardiac Arrest 67 0.101
92
P ATR011 Atrial Fibrillation 66 0.100
93
BRN024 Bronchitis 68 0.100
94
P HDC001 Headache 57 0.100
95
P NPH012 Nephrotic Syndrome 60 0.099
96
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.098
97
LPP008 Lipoprotein Quantitative Trait Locus 62 0.098
98
OST159 Osteogenic Sarcoma 66 0.098
99
c MCR113 Microvascular Complications of Diabetes 3 52 0.097
100
c MCR130 Microvascular Complications of Diabetes 6 41 0.097
101
c MCR133 Microvascular Complications of Diabetes 4 41 0.097
102
P LVR013 Liver Disease 68 0.096
103
P PNC025 Panic Disorder 53 0.096
104
P HYP086 Hypothyroidism 69 0.096
105
MSC007 Muscle Hypertrophy 64 0.094
106
CNT047 Contact Dermatitis 58 0.093
107
STT001 Status Epilepticus 60 0.093
108
INT007 Intermediate Coronary Syndrome 55 0.093
109
ART140 Arteries, Anomalies of 52 0.093
110
P PLM037 Pulmonary Hypertension 67 0.092
111
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.091
112
ATH013 Atherosclerosis Susceptibility 65 0.091
113
c MCR129 Microvascular Complications of Diabetes 1 66 0.090
114
BRN071 Brain Injury 49 0.090
115
P MCR115 Microvascular Complications of Diabetes 5 66 0.089
116
CYT002 Cytokine Deficiency 42 0.089
117
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.089
118
c FNC043 Fanconi Anemia, Complementation Group E 62 0.089
119
IMP005 Impotence 52 0.089
120
P MDL005 Medulloblastoma 77 0.088
121
GLC003 Glucose Intolerance 54 0.086
122
P PNM007 Pneumonia 68 0.085
123
P OPT006 Optic Nerve Disease 60 0.085
124
P OPT009 Optic Neuritis 57 0.084
125
NRT004 Neuritis 52 0.084
126
BNR002 Bone Resorption Disease 48 0.083
127
CMM005 Common Cold 57 0.082
128
P ENC018 Encephalopathy 61 0.081
129
P FBR017 Fibrosarcoma 56 0.081
130
TRM010 Traumatic Brain Injury 51 0.081
131
P EPL164 Epilepsy 71 0.079
132
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.079
133
P VSC007 Vascular Disease 63 0.078
134
c FML035 Familial Hyperlipidemia 55 0.078
135
IRN002 Iron Metabolism Disease 57 0.077
136
ALL010 Allergic Contact Dermatitis 56 0.076
137
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.076
138
AGN016 Aging 56 0.075
139
HYP056 Hypoglycemia 66 0.075
140
ILS001 Ileus 51 0.075
141
P RNL007 Renal Tubular Acidosis 51 0.074
142
P INF038 Influenza 68 0.074
143
P SLP006 Sleep Apnea 69 0.074
144
c FML001 Familial Atrial Fibrillation 65 0.074
145
ATR057 Atrioventricular Block 55 0.074
146
LPD008 Lipid Metabolism Disorder 62 0.073
147
CHL014 Cholera 59 0.073
148
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.073
149
c HPT001 Hepatitis C 62 0.073
150
c ACT075 Acute Myocardial Infarction 57 0.071
151
P CTR002 Cataract 60 0.071
152
SCL003 Social Phobia 48 0.071
153
c ATR087 Atrial Standstill 1 75 0.070
154
P PHC003 Pheochromocytoma 71 0.070
155
P BND020 Bone Disease 59 0.070
156
ADR040 Adrenal Gland Pheochromocytoma 46 0.070
157
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.069
158
P PLY018 Polycythemia 56 0.068
159
P BRS044 Breast Adenocarcinoma 59 0.068
160
SNS003 Sensory Peripheral Neuropathy 54 0.068
161
CRB004 Cerebral Artery Occlusion 45 0.068
162
GNR004 Generalized Anxiety Disorder 56 0.067
163
PPL001 Papillary Adenoma 44 0.067
164
DMY004 Demyelinating Disease 52 0.067
165
HYP540 Hypertension, Diastolic 40 0.067
166
RCK004 Rickets 68 0.066
167
GST023 Gastric Ulcer 53 0.066
168
MCN017 Meconium Ileus 52 0.066
169
P CYS018 Cystitis 59 0.065
170
APN008 Apnea, Obstructive Sleep 64 0.064
171
c PRM005 Primary Hyperparathyroidism 58 0.064
172
c MCR112 Microvascular Complications of Diabetes 2 41 0.064
173
P OCL013 Oculodentodigital Dysplasia 69 0.063
174
NPH009 Nephrolithiasis 55 0.063
175
ANX004 Anoxia 40 0.063
176
c HPT073 Hepatitis C Virus 72 0.062
177
BRN004 Brain Edema 56 0.062
178
HYP081 Hypolipoproteinemia 51 0.062
179
FBR012 Fabry Disease 72 0.062
180
c PRC016 Pre-Eclampsia 63 0.060
181
HLX001 Helix Syndrome 47 0.060
182
GST092 Gastroesophageal Reflux 67 0.060
183
c ACT071 Acute Kidney Failure 60 0.059
184
P PLY014 Polycystic Kidney Disease 62 0.058
185
PPT005 Peptic Ulcer Disease 59 0.057
186
MCL006 Macular Retinal Edema 55 0.057
187
P LCT001 Lactic Acidosis 51 0.057
188
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.056
189
PRT036 Peritonitis 64 0.055
190
URN010 Urinary Tract Obstruction 55 0.055
192
CNN003 Conn's Syndrome 79 0.055
193
HPT019 Hepatic Encephalopathy 60 0.053
194
CCN001 Cocaine Dependence 48 0.053
195
HPT004 Hepatic Coma 45 0.053
196
SPP011 Suppression of Tumorigenicity 12 59 0.052
197
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.052
198
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.052
199
c DLT002 Dilated Cardiomyopathy 79 0.051
200
P INT143 Interstitial Cystitis 61 0.051
201
SYN007 Synovitis 54 0.051
202
PLC002 Plica Syndrome 36 0.051
203
P GLM007 Glomerulonephritis 57 0.049
204
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.049
205
P MSC003 Muscular Atrophy 52 0.049
206
HYP014 Hyperuricemia 52 0.047
207
NPH003 Nephrocalcinosis 51 0.047
208
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.047
209
CRN019 Coronary Artery Vasospasm 46 0.047
210
CRT015 Carotid Artery Occlusion 45 0.047
211
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.047
212
NRM005 Neuromuscular Disease 64 0.047
213
c SVR001 Severe Acute Respiratory Syndrome 62 0.047
214
GST045 Gastroenteritis 59 0.047
215
CRD132 Cardiac Conduction Defect 58 0.047
216
P HYP024 Hypoparathyroidism 56 0.047
217
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.044
218
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.044
219
INS001 Insulinoma 60 0.044
220
MNR012 Meniere Disease 57 0.044
221
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.044
222
P HYP076 Hyperthyroidism 55 0.044
223
SPL018 Splenomegaly 48 0.044
224
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.044
225
AGR002 Agoraphobia 45 0.044
226
P MYC008 Myocarditis 59 0.041
227
MTH009 Mouth Disease 56 0.041
228
P TMP001 Temporal Lobe Epilepsy 50 0.041
229
INP001 Inappropriate Adh Syndrome 49 0.041
230
ATS010 Autosomal Recessive Disease 48 0.041
231
DBT006 Diabetic Macular Edema 48 0.041
232
CRN027 Corneal Neovascularization 47 0.041
233
URT010 Ureteral Obstruction 45 0.041
234
c PCH010 Pachyonychia Congenita 3 44 0.041
235
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.041
236
ADR057 Adrenogenital Syndrome 32 0.041
237
ADG002 Audiogenic Seizures 25 0.041
238
P SPN046 Spinal Muscular Atrophy 62 0.036
239
HYD002 Hydronephrosis 60 0.036
240
PRT013 Portal Hypertension 59 0.036
241
c SPN393 Spinal Muscular Atrophy, Type I 52 0.036
242
c PRM108 Primary Progressive Multiple Sclerosis 51 0.036
243
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.036
244
OBS082 Obstructive Nephropathy 42 0.036
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