Search results for Amiloride

290 hits were found for Amiloride

# Family MCID Name MIFTS Score
1
P ANT061 Antenatal Bartter Syndrome 40 2.923
2
c HYP595 Hypertension, Essential 84 0.347
3
CYS001 Cystic Fibrosis 80 0.280
4
HYP005 Hypokalemia 55 0.277
5
P KDN018 Kidney Disease 70 0.170
6
CNG034 Congestive Heart Failure 70 0.166
7
P DBT005 Diabetes Insipidus 55 0.161
8
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.157
9
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.147
10
LVR012 Liver Cirrhosis 63 0.142
11
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.142
12
LNG099 Lung Disease 61 0.137
13
c CHR684 Chronic Kidney Disease 66 0.126
14
P CRD246 Cardiovascular System Disease 56 0.126
15
PRT037 Pertussis 65 0.120
16
STR067 Stroke, Ischemic 80 0.114
17
P MLT020 Multiple Sclerosis 72 0.114
18
CRB039 Cerebrovascular Disease 69 0.114
19
P GLM045 Glioma 63 0.114
20
ISC004 Ischemia 60 0.114
21
MTB004 Metabolic Acidosis 50 0.114
22
GLL048 Glial Tumor 45 0.114
23
P HRT032 Heart Disease 75 0.108
24
P MYC007 Myocardial Infarction 70 0.108
25
P NPH012 Nephrotic Syndrome 63 0.108
26
P OPT009 Optic Neuritis 56 0.108
27
PLM010 Pulmonary Edema 55 0.108
28
NRT004 Neuritis 53 0.108
29
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.101
30
ANX010 Anxiety 72 0.101
31
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.101
32
P SZR006 Seizure Disorder 58 0.101
33
VSL002 Visual Epilepsy 58 0.101
34
P PSD003 Pseudohypoaldosteronism 45 0.101
35
ANG054 Angina Pectoris 66 0.093
36
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.093
37
STT001 Status Epilepticus 59 0.093
38
P LDD007 Liddle Syndrome 1 59 0.093
39
P OPT006 Optic Nerve Disease 57 0.093
40
c MCR113 Microvascular Complications of Diabetes 3 52 0.093
41
P RNL007 Renal Tubular Acidosis 50 0.093
42
c MCR120 Microvascular Complications of Diabetes 7 47 0.093
43
c MCR130 Microvascular Complications of Diabetes 6 41 0.093
44
c MCR133 Microvascular Complications of Diabetes 4 41 0.093
45
48X005 48,xyyy 39 0.093
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.085
47
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.085
48
P CRD119 Cardiac Arrest 67 0.085
49
MSC007 Muscle Hypertrophy 63 0.085
50
P CRN018 Coronary Artery Anomaly 63 0.085
51
P CRN300 Coronary Heart Disease 1 63 0.085
52
HYP066 Hyperglycemia 61 0.085
53
INT007 Intermediate Coronary Syndrome 55 0.085
54
GLC003 Glucose Intolerance 54 0.085
55
ART140 Arteries, Anomalies of 53 0.085
56
IDP033 Idiopathic Edema 43 0.085
57
P DST107 Distal Renal Tubular Acidosis 41 0.085
58
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.085
59
GLB015 Glioblastoma Multiforme 75 0.076
60
P NRB001 Neuroblastoma 71 0.076
61
c MGR028 Migraine with or Without Aura 1 69 0.076
62
ADL002 Adult Syndrome 69 0.076
63
P PLM037 Pulmonary Hypertension 68 0.076
64
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.076
65
P MCR115 Microvascular Complications of Diabetes 5 66 0.076
66
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.076
67
ATH013 Atherosclerosis Susceptibility 66 0.076
68
P DBT009 Diabetes Mellitus 64 0.076
69
SPN186 Spinal Cord Injury 60 0.076
70
ADN018 Adenoma 58 0.076
71
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.076
72
END030 End Stage Renal Failure 58 0.076
73
HYP266 Hypoxia 56 0.076
74
c FML035 Familial Hyperlipidemia 55 0.076
75
CHL014 Cholera 55 0.076
76
P PNC025 Panic Disorder 53 0.076
77
DMY004 Demyelinating Disease 52 0.076
78
BNR002 Bone Resorption Disease 48 0.076
79
HYP540 Hypertension, Diastolic 40 0.076
80
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.076
81
c ATM100 Autoimmune Optic Neuritis 31 0.076
82
P CLR023 Colorectal Cancer 98 0.066
83
P OCL013 Oculodentodigital Dysplasia 69 0.066
84
P HYP086 Hypothyroidism 68 0.066
85
BRN024 Bronchitis 68 0.066
86
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.066
87
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.066
88
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.066
89
DPR016 Depression 63 0.066
90
P HDC001 Headache 57 0.066
91
MNT002 Mental Depression 57 0.066
92
P NRP001 Neuropathy 56 0.066
93
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.066
94
P MGR003 Migraine with Aura 50 0.066
95
c MLG068 Malignant Glioma 45 0.066
96
c PRM038 Primary Agammaglobulinemia 43 0.066
97
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.066
98
49X006 49, Xxxxy Syndrome 41 0.066
99
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.066
100
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.066
101
P PNC035 Pancreatic Cancer 84 0.054
102
CNN003 Conn's Syndrome 79 0.054
103
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.054
104
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.054
105
c HPT073 Hepatitis C Virus 70 0.054
106
RCK004 Rickets 69 0.054
107
P SLP006 Sleep Apnea 69 0.054
108
c FML001 Familial Atrial Fibrillation 66 0.054
109
P ATR011 Atrial Fibrillation 66 0.054
110
c MCR129 Microvascular Complications of Diabetes 1 66 0.054
111
GTL001 Gitelman Syndrome 66 0.054
112
c RHB024 Rhabdomyosarcoma 2 65 0.054
113
GST092 Gastroesophageal Reflux 65 0.054
114
APN008 Apnea, Obstructive Sleep 65 0.054
115
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.054
116
ALL026 Allergic Hypersensitivity Disease 64 0.054
117
P ADN016 Adenocarcinoma 64 0.054
118
c HPT001 Hepatitis C 63 0.054
119
P HYP069 Hyperparathyroidism 62 0.054
120
c FNC043 Fanconi Anemia, Complementation Group E 62 0.054
121
NTR005 Nutritional Deficiency Disease 61 0.054
122
c HYP731 Hyperaldosteronism, Familial, Type I 60 0.054
123
DCB001 Decubitus Ulcer 60 0.054
124
SPP011 Suppression of Tumorigenicity 12 59 0.054
125
P PLY014 Polycystic Kidney Disease 59 0.054
126
P BRS044 Breast Adenocarcinoma 59 0.054
127
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 58 0.054
128
c PRM005 Primary Hyperparathyroidism 58 0.054
129
IRN002 Iron Metabolism Disease 57 0.054
130
P EXN002 Exanthem 57 0.054
131
ERY051 Erythroleukemia, Familial 56 0.054
132
c ACT075 Acute Myocardial Infarction 56 0.054
133
AGN016 Aging 56 0.054
134
RHM027 Rheumatic Disease 56 0.054
135
ADR008 Adrenal Adenoma 56 0.054
136
BRN004 Brain Edema 55 0.054
137
ATR057 Atrioventricular Block 55 0.054
138
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.054
139
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.054
140
SNS003 Sensory Peripheral Neuropathy 53 0.054
141
TRM010 Traumatic Brain Injury 53 0.054
142
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.054
143
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.054
144
NPH003 Nephrocalcinosis 51 0.054
145
HYP014 Hyperuricemia 51 0.054
146
HYP081 Hypolipoproteinemia 50 0.054
147
BRN071 Brain Injury 49 0.054
148
47X002 47,xyy 49 0.054
149
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.054
150
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.054
151
INT067 Interstitial Nephritis 46 0.054
152
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.054
153
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.054
154
CRN019 Coronary Artery Vasospasm 46 0.054
155
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.054
156
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.054
157
CRB004 Cerebral Artery Occlusion 44 0.054
158
CRT015 Carotid Artery Occlusion 44 0.054
159
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.054
160
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.054
161
CRB090 Cerebral Hypoxia 43 0.054
162
ADR041 Adrenal Cortical Adenoma 43 0.054
163
c MCR112 Microvascular Complications of Diabetes 2 41 0.054
164
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.054
165
P FML187 Familial Hypertension 37 0.054
166
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.054
167
c RNG015 Ring Chromosome 2 26 0.054
168
LTH043 Lithium Transport 18 0.054
169
P LNG032 Lung Cancer 97 0.038
170
ESP021 Esophageal Cancer 90 0.038
171
P OVR042 Ovarian Cancer 89 0.038
172
MYL069 Myeloma, Multiple 85 0.038
173
P GST053 Gastric Cancer 83 0.038
174
c DLT002 Dilated Cardiomyopathy 79 0.038
175
P MDL005 Medulloblastoma 77 0.038
176
c ATR087 Atrial Standstill 1 74 0.038
177
P PHC003 Pheochromocytoma 71 0.038
178
P EPL164 Epilepsy 71 0.038
179
c LKM063 Leukemia, Chronic Myeloid 71 0.038
180
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.038
181
FBR012 Fabry Disease 71 0.038
182
HMN044 Human Immunodeficiency Virus Type 1 71 0.038
183
ACR007 Acromegaly 71 0.038
184
P LVR013 Liver Disease 68 0.038
185
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.038
186
P ALP004 Alport Syndrome 68 0.038
187
P INF038 Influenza 68 0.038
188
P PNM007 Pneumonia 68 0.038
189
OST159 Osteogenic Sarcoma 66 0.038
190
HYP056 Hypoglycemia 66 0.038
191
PRT036 Peritonitis 65 0.038
192
P SPN046 Spinal Muscular Atrophy 64 0.038
193
CLN015 Colon Adenocarcinoma 63 0.038
194
P VSC007 Vascular Disease 63 0.038
195
c PRC016 Pre-Eclampsia 63 0.038
196
NRM005 Neuromuscular Disease 63 0.038
197
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.038
198
LPD008 Lipid Metabolism Disorder 62 0.038
199
DRM006 Dermatitis 61 0.038
200
P INT143 Interstitial Cystitis 61 0.038
201
P ENC018 Encephalopathy 61 0.038
202
PRT013 Portal Hypertension 60 0.038
203
P CTR002 Cataract 60 0.038
204
HPT019 Hepatic Encephalopathy 60 0.038
205
INS001 Insulinoma 60 0.038
206
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.038
207
P MYC008 Myocarditis 59 0.038
208
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 59 0.038
209
c ACT071 Acute Kidney Failure 59 0.038
210
HYD002 Hydronephrosis 59 0.038
211
P CYS018 Cystitis 59 0.038
212
P BND020 Bone Disease 59 0.038
213
GST045 Gastroenteritis 59 0.038
214
CRD132 Cardiac Conduction Defect 59 0.038
215
PPT005 Peptic Ulcer Disease 58 0.038
216
P FCL005 Focal Segmental Glomerulosclerosis 58 0.038
217
CNT047 Contact Dermatitis 57 0.038
218
URN010 Urinary Tract Obstruction 57 0.038
219
MNR012 Meniere Disease 57 0.038
220
BRN056 Bronchopulmonary Dysplasia 57 0.038
221
P GLM007 Glomerulonephritis 57 0.038
222
P FBR017 Fibrosarcoma 56 0.038
223
TRN018 Transitional Cell Carcinoma 56 0.038
224
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.038
225
GNR004 Generalized Anxiety Disorder 56 0.038
226
CMM005 Common Cold 56 0.038
227
MTH009 Mouth Disease 56 0.038
228
SYN007 Synovitis 55 0.038
229
P HYP024 Hypoparathyroidism 55 0.038
230
c SVR001 Severe Acute Respiratory Syndrome 55 0.038
231
MCL006 Macular Retinal Edema 55 0.038
232
P PLY018 Polycythemia 55 0.038
233
ALL010 Allergic Contact Dermatitis 55 0.038
234
P HYP076 Hyperthyroidism 55 0.038
235
c SPN393 Spinal Muscular Atrophy, Type I 53 0.038
236
GST023 Gastric Ulcer 53 0.038
237
MCN017 Meconium Ileus 52 0.038
238
c GLL024 Gallbladder Disease 1 52 0.038
239
IMP005 Impotence 52 0.038
240
P MSC003 Muscular Atrophy 52 0.038
241
OVR059 Ovary Adenocarcinoma 51 0.038
242
P HYP210 Hypomagnesemia 2, Renal 51 0.038
243
ILS001 Ileus 51 0.038
244
P FBR031 Febrile Seizures 51 0.038
245
P LCT001 Lactic Acidosis 51 0.038
246
c PRM108 Primary Progressive Multiple Sclerosis 51 0.038
247
P TMP001 Temporal Lobe Epilepsy 50 0.038
248
P AST007 Astrocytoma 50 0.038
249
P CHR345 Chronic Pain 50 0.038
250
INP001 Inappropriate Adh Syndrome 49 0.038
251
CCN001 Cocaine Dependence 48 0.038
252
DBT006 Diabetic Macular Edema 48 0.038
253
SCL003 Social Phobia 48 0.038
254
ATS010 Autosomal Recessive Disease 48 0.038
255
IGG001 Iga Glomerulonephritis 48 0.038
256
ATX019 Ataxia with Vitamin E Deficiency 48 0.038
257
c SPL067 Split-Hand/foot Malformation 1 48 0.038
258
SPL018 Splenomegaly 48 0.038
259
HLX001 Helix Syndrome 47 0.038
260
CRN027 Corneal Neovascularization 47 0.038
261
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.038
262
ISL121 Isolated Split Hand-Split Foot Malformation 46 0.038
263
ADR040 Adrenal Gland Pheochromocytoma 46 0.038
264
MYC005 Myocardial Stunning 46 0.038
265
URT010 Ureteral Obstruction 46 0.038
266
P HYP733 Hypercalciuria, Absorptive, 2 46 0.038
267
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.038
268
HMR002 Hemarthrosis 45 0.038
269
PPL001 Papillary Adenoma 45 0.038
270
AGR002 Agoraphobia 44 0.038
271
CYT002 Cytokine Deficiency 44 0.038
272
c PCH010 Pachyonychia Congenita 3 43 0.038
273
HPT004 Hepatic Coma 43 0.038
274
OBS082 Obstructive Nephropathy 43 0.038
275
IDP074 Idiopathic Bronchiectasis 43 0.038
276
ANX004 Anoxia 42 0.038
277
MST004 Mast Cell Neoplasm 38 0.038
278
EXT007 Extracutaneous Mastocytoma 38 0.038
279
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.038
280
c MLN043 Melanoma, Cutaneous Malignant 8 35 0.038
282
ADR057 Adrenogenital Syndrome 32 0.038
283
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.038
284
ARG004 Argyria 28 0.038
285
PRR019 Perioral Myoclonia with Absences 28 0.038
286
c HRD219 Hereditary Distal Renal Tubular Acidosis 26 0.038
287
ADG002 Audiogenic Seizures 26 0.038
288
PLM061 Pulmonary Edema of Mountaineers 25 0.038
289
c BRN075 Bronchiectasis with or Without Elevated Sweat Chloride 2 23 0.038
290
OBN001 Ouabain Resistance 18 0.038
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