Search results for Hydrochlorothiazide

361 hits were found for Hydrochlorothiazide

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 1.003
2
HYP005 Hypokalemia 55 0.428
3
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.308
4
P KDN018 Kidney Disease 70 0.283
5
CNG034 Congestive Heart Failure 70 0.268
6
P DBT005 Diabetes Insipidus 55 0.252
7
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.250
8
ADL002 Adult Syndrome 69 0.227
9
P DBT009 Diabetes Mellitus 64 0.222
10
P CRD246 Cardiovascular System Disease 56 0.219
11
P HRT032 Heart Disease 75 0.217
12
CRB039 Cerebrovascular Disease 69 0.217
13
PLM010 Pulmonary Edema 55 0.214
14
c CHR684 Chronic Kidney Disease 66 0.208
15
P TRN020 Turner Syndrome 65 0.203
16
STR067 Stroke, Ischemic 80 0.191
17
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.181
18
48X005 48,xyyy 39 0.175
19
HYP014 Hyperuricemia 51 0.171
20
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.164
21
HYP540 Hypertension, Diastolic 40 0.164
22
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.161
23
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.161
24
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.161
25
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.161
26
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.161
27
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.161
28
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.161
29
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.161
30
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.161
31
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.161
32
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.161
33
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.161
34
P MYC007 Myocardial Infarction 70 0.157
35
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.153
36
c RHB024 Rhabdomyosarcoma 2 65 0.149
37
LPD008 Lipid Metabolism Disorder 62 0.149
38
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.145
39
c MCR113 Microvascular Complications of Diabetes 3 52 0.141
40
c MCR120 Microvascular Complications of Diabetes 7 47 0.141
41
c MCR130 Microvascular Complications of Diabetes 6 41 0.141
42
c MCR133 Microvascular Complications of Diabetes 4 41 0.141
43
P VSC007 Vascular Disease 63 0.133
44
NTR005 Nutritional Deficiency Disease 61 0.133
45
LVR012 Liver Cirrhosis 63 0.128
46
P SKN015 Skin Carcinoma 67 0.124
47
MSC007 Muscle Hypertrophy 63 0.124
48
PRT058 Pure Autonomic Failure 59 0.124
49
IDP073 Idiopathic Hypercalciuria 43 0.124
50
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.119
51
DWN001 Down Syndrome 70 0.119
52
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.119
53
GLC003 Glucose Intolerance 54 0.119
54
P HYP733 Hypercalciuria, Absorptive, 2 46 0.119
55
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.114
56
P CRN018 Coronary Artery Anomaly 63 0.114
57
P CRN300 Coronary Heart Disease 1 63 0.114
58
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.114
59
RCK004 Rickets 69 0.108
60
GT001 Gout 63 0.108
61
P NPH012 Nephrotic Syndrome 63 0.108
62
P HYP069 Hyperparathyroidism 62 0.108
63
IMP005 Impotence 52 0.108
64
47X002 47,xyy 49 0.108
65
P LVR013 Liver Disease 68 0.103
66
P MCR115 Microvascular Complications of Diabetes 5 66 0.103
67
P HYP024 Hypoparathyroidism 55 0.103
68
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.103
69
c HYP836 Hypercholesterolemia, Familial, 1 72 0.097
70
c ACT071 Acute Kidney Failure 59 0.097
71
P EXN002 Exanthem 57 0.097
72
NPH003 Nephrocalcinosis 51 0.097
73
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.097
74
PRP027 Peripheral Vascular Disease 71 0.091
75
c MCR129 Microvascular Complications of Diabetes 1 66 0.091
76
HYP066 Hyperglycemia 61 0.091
77
P LPS004 Lupus Erythematosus 61 0.091
78
CRD132 Cardiac Conduction Defect 59 0.091
79
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.091
80
ART140 Arteries, Anomalies of 53 0.091
81
PRP080 Peripheral Artery Disease 53 0.091
82
c MCR112 Microvascular Complications of Diabetes 2 41 0.091
83
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.091
84
P OST002 Osteoporosis 73 0.084
85
P SLP006 Sleep Apnea 69 0.084
86
ANG054 Angina Pectoris 66 0.084
87
P NTR004 Neutropenia 63 0.084
88
ISC004 Ischemia 60 0.084
89
c PRM005 Primary Hyperparathyroidism 58 0.084
90
INT007 Intermediate Coronary Syndrome 55 0.084
91
SXL003 Sexual Disorder 48 0.084
92
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.084
93
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.084
94
LPT014 Leptin Deficiency or Dysfunction 73 0.077
95
MLN008 Melanoma 69 0.077
96
c FML001 Familial Atrial Fibrillation 66 0.077
97
P ATR011 Atrial Fibrillation 66 0.077
98
ATH013 Atherosclerosis Susceptibility 66 0.077
99
APN008 Apnea, Obstructive Sleep 65 0.077
100
ALL026 Allergic Hypersensitivity Disease 64 0.077
101
P DNT020 Dent Disease 1 60 0.077
102
P OPT006 Optic Nerve Disease 57 0.077
103
P GLM007 Glomerulonephritis 57 0.077
104
AGN016 Aging 56 0.077
105
c FML035 Familial Hyperlipidemia 55 0.077
106
P CTN003 Cutaneous Lupus Erythematosus 52 0.077
107
HYP081 Hypolipoproteinemia 50 0.077
108
c INF145 Infantile Liver Failure Syndrome 1 50 0.077
109
BNR002 Bone Resorption Disease 48 0.077
110
P RNL015 Renal Hypertension 48 0.077
111
ATX019 Ataxia with Vitamin E Deficiency 48 0.077
112
TRP009 Triple X Syndrome 42 0.077
113
c SBC035 Subacute Cutaneous Lupus Erythematosus 33 0.077
114
P HYP086 Hypothyroidism 68 0.069
115
P DMN002 Dementia 67 0.069
116
GTL001 Gitelman Syndrome 66 0.069
117
KHL003 Kohlschutter-Tonz Syndrome 64 0.069
118
P PRM002 Primary Hyperoxaluria 62 0.069
119
P PNC044 Pancreatitis 61 0.069
120
P ALC033 Alcohol Use Disorder 58 0.069
121
END030 End Stage Renal Failure 58 0.069
122
P NRP001 Neuropathy 56 0.069
123
P BRT004 Bartter Disease 55 0.069
124
P FNC004 Fanconi Syndrome 50 0.069
125
LPT006 Leptin Receptor Deficiency 47 0.069
126
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.069
127
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.069
128
ATN004 Autonomic Neuropathy 44 0.069
129
IDP033 Idiopathic Edema 43 0.069
130
NSP002 Nasopharyngitis 41 0.069
131
RST023 Resting Heart Rate, Variation in 41 0.069
132
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 0.069
133
TLM001 Telomere Length, Mean Leukocyte 19 0.069
134
P MLT020 Multiple Sclerosis 72 0.059
135
c BSL007 Basal Cell Carcinoma 68 0.059
136
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.059
137
P THR014 Thrombocytopenia 68 0.059
138
c PRC016 Pre-Eclampsia 63 0.059
139
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.059
140
BLL006 Bullous Pemphigoid 62 0.059
141
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.059
142
TXC005 Toxic Shock Syndrome 61 0.059
143
P HYP750 Hypertriglyceridemia, Familial 61 0.059
144
P ENC018 Encephalopathy 61 0.059
145
CYS010 Cystinosis 60 0.059
146
P BND020 Bone Disease 59 0.059
147
RNL024 Renal Glucosuria 57 0.059
148
P RHN004 Rhinitis 57 0.059
149
DSS008 Disease of Mental Health 57 0.059
150
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.059
151
P DRR001 Diarrhea 57 0.059
152
P OPT009 Optic Neuritis 56 0.059
153
PRP030 Purpura 55 0.059
154
P MYP006 Myopia 55 0.059
155
P ANG015 Angioedema 54 0.059
156
NRT004 Neuritis 53 0.059
157
HMC014 Homocysteinemia 53 0.059
158
DMY004 Demyelinating Disease 52 0.059
159
CYS036 Cystinosis, Nephropathic 51 0.059
160
P ECL001 Eclampsia 51 0.059
161
P PRC012 Pericardial Effusion 51 0.059
162
c SCN007 Secondary Hyperparathyroidism 50 0.059
163
CRT013 Carotid Stenosis 50 0.059
164
P RNL007 Renal Tubular Acidosis 50 0.059
165
NPH010 Nephrosclerosis 49 0.059
166
P RNV001 Renovascular Hypertension 49 0.059
167
PRD004 Prediabetes Syndrome 47 0.059
168
c MLG069 Malignant Hypertension 47 0.059
169
INT067 Interstitial Nephritis 46 0.059
170
HMP001 Hemopericardium 46 0.059
171
P LPC002 Lip Cancer 45 0.059
172
CYT002 Cytokine Deficiency 44 0.059
173
c HYP272 Hypercholesterolemia, Familial, 3 43 0.059
174
LWC001 Low Compliance Bladder 42 0.059
175
DBT002 Diabetic Autonomic Neuropathy 41 0.059
176
GST020 Gastric Antral Vascular Ectasia 41 0.059
177
49X006 49, Xxxxy Syndrome 41 0.059
178
RDN001 Reading Disorder 40 0.059
179
GLM044 Glomerular Disease 39 0.059
180
AMN006 Aminoaciduria 38 0.059
181
P PRC031 Preeclampsia/eclampsia 1 37 0.059
182
c ATM100 Autoimmune Optic Neuritis 31 0.059
183
URT049 Urate Oxidase, Pseudogene 25 0.059
184
DFC004 Deficiency Anemia 75 0.048
185
P RSP003 Respiratory Failure 74 0.048
186
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.048
187
ANX010 Anxiety 72 0.048
188
MLT157 Multiple System Atrophy 1 70 0.048
189
P CRD119 Cardiac Arrest 67 0.048
190
PSY004 Psychotic Disorder 67 0.048
191
ALC007 Alcohol Dependence 66 0.048
192
DPR016 Depression 63 0.048
193
P ADL010 Adult Respiratory Distress Syndrome 63 0.048
194
c ACT068 Acute Cystitis 63 0.048
195
ANR007 Anorexia Nervosa 63 0.048
196
P HML002 Hemolytic Anemia 62 0.048
197
c FNC043 Fanconi Anemia, Complementation Group E 62 0.048
198
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.048
199
MDD011 Mood Disorder 62 0.048
200
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.048
201
P PLY014 Polycystic Kidney Disease 59 0.048
202
ADN018 Adenoma 58 0.048
203
CHL067 Cholecystitis 58 0.048
204
MNR012 Meniere Disease 57 0.048
205
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.048
206
MNT002 Mental Depression 57 0.048
207
P HYP726 Hypercalcemia, Infantile, 1 57 0.048
208
P HYP076 Hyperthyroidism 55 0.048
209
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.048
210
P ART021 Arteriosclerosis 54 0.048
211
AMN001 Amenorrhea 54 0.048
212
P TRM003 Tremor 53 0.048
213
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.048
214
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.048
215
PRS045 Prostatic Hypertrophy 52 0.048
216
PRS021 Prostatic Adenoma 51 0.048
217
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.048
218
MTB004 Metabolic Acidosis 50 0.048
219
HYP006 Hypertensive Heart Disease 49 0.048
220
PRS129 Prostatic Hyperplasia, Benign 49 0.048
221
c HNT004 Huntington Disease-Like 2 49 0.048
222
HYP025 Hyperphosphatemia 47 0.048
223
P PRD021 Periodic Paralysis 46 0.048
224
SYN036 Syncope 45 0.048
225
P END084 Endocrine System Disease 44 0.048
226
GLC008 Glucose Metabolism Disease 40 0.048
227
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.048
228
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.048
229
c HNT011 Huntington Disease-Like 3 38 0.048
230
c BNG021 Benign Essential Hypertension 37 0.048
231
P ACT028 Acute Closed-Angle Glaucoma 28 0.048
232
SCN001 Secondary Hyperparathyroidism of Renal Origin 28 0.048
233
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.048
234
c SYS001 Systemic Lupus Erythematosus 86 0.034
235
c DLT002 Dilated Cardiomyopathy 79 0.034
236
OST012 Osteoarthritis 78 0.034
237
AST005 Asthma 77 0.034
238
P NRF023 Neurofibromatosis, Type Ii 76 0.034
239
P APL001 Aplastic Anemia 74 0.034
240
c ATR087 Atrial Standstill 1 74 0.034
241
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.034
242
P PHC003 Pheochromocytoma 71 0.034
243
P SRC025 Sarcoidosis 1 70 0.034
244
c MGR028 Migraine with or Without Aura 1 69 0.034
245
ART016 Aortic Aneurysm 68 0.034
246
P PLM037 Pulmonary Hypertension 68 0.034
247
BRN024 Bronchitis 68 0.034
248
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.034
249
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.034
250
P HYP061 Hypertrophic Cardiomyopathy 66 0.034
251
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.034
252
HYP056 Hypoglycemia 66 0.034
253
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.034
254
P HYP098 Hypereosinophilic Syndrome 66 0.034
255
MRK001 Merkel Cell Carcinoma 66 0.034
256
MYC006 Mycosis Fungoides 66 0.034
257
WLF001 Wolff-Parkinson-White Syndrome 65 0.034
258
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.034
259
P HRP006 Herpes Simplex 65 0.034
260
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.034
261
TBC004 Tobacco Addiction 64 0.034
262
CLN015 Colon Adenocarcinoma 63 0.034
263
c ART101 Aortic Valve Disease 2 63 0.034
264
P ORT004 Orthostatic Intolerance 63 0.034
265
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.034
266
P PSR002 Psoriasis 62 0.034
267
P VSC011 Vasculitis 62 0.034
268
INT002 Intermittent Claudication 61 0.034
269
FTT001 Fatty Liver Disease 61 0.034
270
c BRN108 Branchiootic Syndrome 1 61 0.034
271
RTN017 Retinal Detachment 60 0.034
272
SQM006 Squamous Cell Carcinoma 60 0.034
273
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.034
274
THY029 Thyroid Carcinoma 59 0.034
275
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 59 0.034
276
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.034
277
c ACT027 Acute Pancreatitis 59 0.034
278
HYD002 Hydronephrosis 59 0.034
279
GST045 Gastroenteritis 59 0.034
280
PLM033 Pulmonary Embolism 59 0.034
281
P INT070 Intestinal Obstruction 58 0.034
282
ANR040 Aneurysm 58 0.034
283
P PLY017 Polyarteritis Nodosa 58 0.034
284
P SZR006 Seizure Disorder 58 0.034
285
VSL002 Visual Epilepsy 58 0.034
286
NWB001 Newborn Respiratory Distress Syndrome 58 0.034
287
c DWL002 Dowling-Degos Disease 1 58 0.034
288
PMP006 Pemphigus Vulgaris, Familial 58 0.034
289
IRN002 Iron Metabolism Disease 57 0.034
290
BRN056 Bronchopulmonary Dysplasia 57 0.034
291
HMR039 Hemorrhage, Intracerebral 57 0.034
292
VSC002 Vascular Dementia 57 0.034
293
P PYL005 Pyelonephritis 56 0.034
294
HYP266 Hypoxia 56 0.034
295
P PSD015 Pseudohypoparathyroidism 56 0.034
296
P GST044 Gastritis 55 0.034
297
MCL006 Macular Retinal Edema 55 0.034
298
ATR057 Atrioventricular Block 55 0.034
299
P SCK002 Sick Sinus Syndrome 55 0.034
300
c GRV008 Graves Disease 1 55 0.034
301
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.034
302
DBT010 Diabetic Neuropathy 55 0.034
303
P PMP001 Pemphigus 55 0.034
304
P LCH002 Lichen Planus 54 0.034
305
ANL018 Analbuminemia 54 0.034
306
PRC013 Pericarditis 54 0.034
307
c HYP768 Hyperlipoproteinemia, Type I 52 0.034
308
PST011 Pustulosis of Palm and Sole 52 0.034
309
DFF036 Differentiated Thyroid Carcinoma 51 0.034
311
OCL069 Ocular Motor Apraxia 51 0.034
312
c VRL010 Viral Hepatitis 51 0.034
313
MYL020 Myelomeningocele 51 0.034
314
NNL006 Non-Alcoholic Steatohepatitis 51 0.034
315
P MTR003 Mitral Valve Stenosis 50 0.034
316
CHR078 Chorioretinitis 50 0.034
317
DYS073 Dysphagia 50 0.034
318
RLP003 Relapsing Fever 50 0.034
319
P CTN015 Cutaneous T Cell Lymphoma 49 0.034
320
CHL004 Cholelithiasis 49 0.034
321
INP001 Inappropriate Adh Syndrome 49 0.034
322
c HYP243 Hyperparathyroidism 1 49 0.034
323
P MGR001 Migraine Without Aura 48 0.034
324
SPL018 Splenomegaly 48 0.034
325
CRD001 Cardiac Tamponade 46 0.034
326
RYN005 Raynaud Phenomenon 46 0.034
327
ADR040 Adrenal Gland Pheochromocytoma 46 0.034
328
ANR004 Anuria 46 0.034
329
DRG013 Drug-Induced Lupus Erythematosus 46 0.034
330
HYD005 Hydrocele 46 0.034
331
PRM057 Paramyotonia Congenita of Von Eulenburg 46 0.034
332
CNT025 Central Pontine Myelinolysis 45 0.034
333
P PSD003 Pseudohypoaldosteronism 45 0.034
334
ACT003 Acute Kidney Tubular Necrosis 45 0.034
335
THR099 Third-Degree Atrioventricular Block 45 0.034
336
ADR012 Adrenal Gland Disease 45 0.034
337
MYX004 Myxedema 44 0.034
338
CRB025 Carbohydrate Metabolic Disorder 44 0.034
339
GRN017 Granulocytopenia 44 0.034
340
DRG024 Drug Allergy 43 0.034
341
P LBY004 Labyrinthitis 43 0.034
342
BCK006 Back Pain 42 0.034
343
P HYP263 Hypersomnia 41 0.034
344
RTR011 Retroperitoneal Fibrosis 40 0.034
345
c PSD092 Pseudohypoaldosteronism, Type Iie 38 0.034
346
ADR009 Adrenal Cortex Disease 37 0.034
347
P FML187 Familial Hypertension 37 0.034
348
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.034
349
MYT011 Myotonia 35 0.034
350
KDN013 Kidney Hypertrophy 34 0.034
351
GNT167 Genetic Obesity 34 0.034
352
P VSC018 Visceral Steatosis 33 0.034
353
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.034
354
c MLG039 Malignant Essential Hypertension 32 0.034
355
P RNL115 Renal Tubular Acidosis, Proximal 31 0.034
356
PST092 Posttransplant Acute Limbic Encephalitis 29 0.034
357
NRM009 Normokalemic Periodic Paralysis 28 0.034
358
CHL079 Children's Interstitial Lung Disease 27 0.034
359
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.034
360
P PLM064 Pulmonary Sequestration 22 0.034
361
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 18 0.034
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