Search results for Chlorothiazide

182 hits were found for Chlorothiazide

# Family MCID Name MIFTS Score
1
P DBT005 Diabetes Insipidus 54 8.077
2
c HYP595 Hypertension, Essential 85 7.476
3
CNG034 Congestive Heart Failure 69 7.008
4
HYP005 Hypokalemia 55 6.430
5
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 4.312
6
P HRT032 Heart Disease 81 3.517
7
BRN056 Bronchopulmonary Dysplasia 56 2.852
8
IDP073 Idiopathic Hypercalciuria 40 2.596
9
P CRD246 Cardiovascular System Disease 56 2.516
10
BNR002 Bone Resorption Disease 47 2.515
11
P HYP069 Hyperparathyroidism 62 2.462
12
PRP030 Purpura 54 2.350
13
HYP014 Hyperuricemia 51 2.347
14
c ACT071 Acute Kidney Failure 60 2.320
15
URL001 Urolithiasis 46 2.213
16
P HYP024 Hypoparathyroidism 55 2.168
17
OCL069 Ocular Motor Apraxia 57 2.161
18
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 2.107
19
NPH003 Nephrocalcinosis 49 2.099
20
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 38 2.056
21
HPT004 Hepatic Coma 43 1.982
22
HYP066 Hyperglycemia 61 1.956
23
HYP056 Hypoglycemia 65 1.938
24
P NPH012 Nephrotic Syndrome 60 1.913
25
CLF004 Cleft Lip/palate 57 1.679
26
P HLP001 Holoprosencephaly 69 1.679
27
CLF001 Cleft Lip 53 1.679
28
c ACT027 Acute Pancreatitis 60 1.679
29
GT001 Gout 64 1.635
30
HYP060 Hyperinsulinism 54 1.546
31
P PNC044 Pancreatitis 61 1.528
32
LNG099 Lung Disease 62 1.492
33
MTB004 Metabolic Acidosis 48 1.431
34
P PTN014 Patent Ductus Arteriosus 1 59 1.431
35
P VSC007 Vascular Disease 63 1.388
36
P ACN011 Acne 57 1.335
37
SLF016 Sulfonamide Allergy 24 1.307
38
48X005 48,xyyy 39 1.307
39
URT049 Urate Oxidase, Pseudogene 24 1.252
40
P KDN018 Kidney Disease 72 1.252
41
c SCN007 Secondary Hyperparathyroidism 51 1.252
42
HPT019 Hepatic Encephalopathy 59 1.252
43
PLM010 Pulmonary Edema 55 1.252
44
P ENC018 Encephalopathy 62 1.252
45
P THR014 Thrombocytopenia 66 1.156
46
PRM020 Premenstrual Tension 39 1.156
47
DPS001 Dipsogenic Diabetes Insipidus 22 1.156
48
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 1.012
49
P PLM037 Pulmonary Hypertension 72 1.012
50
PRT251 Proteinuria, Chronic Benign 57 1.012
51
GTL001 Gitelman Syndrome 65 1.012
52
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 1.012
53
NPH009 Nephrolithiasis 54 1.012
54
P HYP050 Hyperinsulinemic Hypoglycemia 57 1.012
55
P SZR006 Seizure Disorder 70 0.944
56
P OST002 Osteoporosis 76 0.944
57
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.944
58
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.944
59
c PRC016 Pre-Eclampsia 65 0.944
60
P RNL007 Renal Tubular Acidosis 50 0.944
61
P ECL001 Eclampsia 52 0.944
62
P GLM007 Glomerulonephritis 60 0.944
63
GRN017 Granulocytopenia 42 0.944
64
STR067 Stroke, Ischemic 80 0.826
65
c HYP292 Hypophosphatasia, Infantile 55 0.826
66
OST159 Osteogenic Sarcoma 66 0.826
67
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.826
68
P HYP726 Hypercalcemia, Infantile, 1 58 0.826
69
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 0.826
70
P FML068 Familial Hypocalciuric Hypercalcemia 55 0.826
71
P PMP001 Pemphigus 55 0.826
72
SKN016 Skin Disease 63 0.826
73
CHL004 Cholelithiasis 49 0.826
74
P HYP035 Hypophosphatasia 62 0.826
75
HYD002 Hydronephrosis 58 0.826
76
P BND020 Bone Disease 59 0.826
77
c PRM005 Primary Hyperparathyroidism 59 0.826
78
PRM057 Paramyotonia Congenita of Von Eulenburg 59 0.667
79
ANG054 Angina Pectoris 66 0.667
80
P CRP001 Carpal Tunnel Syndrome 66 0.667
81
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.667
82
c PRM152 Primary Renal Tubular Acidosis 11 0.667
83
P PSR002 Psoriasis 63 0.667
84
P HRP006 Herpes Simplex 65 0.667
85
ANR004 Anuria 44 0.667
86
ILS001 Ileus 50 0.667
87
PRL008 Paralytic Ileus 45 0.667
88
PST011 Pustulosis of Palm and Sole 52 0.667
89
P NTR004 Neutropenia 63 0.667
90
NNT012 Neonatal Jaundice 53 0.667
91
HYP006 Hypertensive Heart Disease 49 0.667
92
c BNG021 Benign Essential Hypertension 35 0.667
93
c JVN025 Juvenile Primary Osteoporosis 21 0.667
94
MYT011 Myotonia 39 0.667
95
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.666
96
CVD001 Covid-19 57 0.666
97
RHB024 Rhabdomyosarcoma 2 67 0.666
98
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.666
99
CRH001 Crohn's Disease 80 0.666
100
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.584
101
ANX004 Anoxia 40 0.584
102
GRW007 Growth Hormone Deficiency 46 0.584
103
c ACT134 Acute Liver Failure 59 0.584
104
P OVR082 Overgrowth Syndrome 49 0.584
105
c DWL002 Dowling-Degos Disease 1 58 0.584
106
MCR334 Microcolon 34 0.584
107
MYC006 Mycosis Fungoides 65 0.584
108
MCR037 Macroglossia 44 0.584
109
c SYS001 Systemic Lupus Erythematosus 87 0.584
110
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.584
111
P BCK002 Beckwith-Wiedemann Syndrome 62 0.584
112
HYP540 Hypertension, Diastolic 37 0.584
114
HYP017 Hypophosphatemia 49 0.584
115
P EXN002 Exanthem 58 0.584
116
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.584
117
WST001 West Syndrome 59 0.584
118
P URN019 Urinary Tract Infection 49 0.584
119
DSM004 Desmoid Tumor 66 0.584
120
ART074 Aortic Dissection 53 0.584
121
CMP034 Complete Androgen Insensitivity Syndrome 55 0.584
122
MYL020 Myelomeningocele 51 0.584
123
P FTL001 Fetal Alcohol Syndrome 55 0.584
124
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 48 0.584
125
P PRP003 Porphyria Cutanea Tarda 66 0.584
126
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.584
127
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.584
128
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.584
129
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.584
130
OST017 Osteomyelitis 63 0.584
131
INT067 Interstitial Nephritis 46 0.584
132
c PSD094 Pseudohypoaldosteronism, Type Iib 26 0.584
133
c PSD092 Pseudohypoaldosteronism, Type Iie 48 0.584
134
PMP014 Pemphigoid 51 0.584
135
P LPS004 Lupus Erythematosus 61 0.584
136
P HYP083 Hypopituitarism 52 0.584
137
SMT003 Somatostatinoma 52 0.584
138
PNC006 Pancreatic Somatostatinoma 27 0.584
139
P DBT009 Diabetes Mellitus 67 0.584
140
PYD001 Pyoderma Gangrenosum 53 0.584
141
P HYP098 Hypereosinophilic Syndrome 66 0.584
142
47X002 47,xyy 48 0.584
143
P RNV001 Renovascular Hypertension 49 0.584
144
P LVR013 Liver Disease 69 0.584
145
ALL010 Allergic Contact Dermatitis 56 0.584
146
INS001 Insulinoma 59 0.584
147
P SYP003 Syphilis 59 0.584
148
PYD002 Pyoderma 50 0.584
149
ART016 Aortic Aneurysm 68 0.584
150
THR016 Thrombophlebitis 50 0.584
151
SPN011 Spongiotic Dermatitis 31 0.584
152
c LCL006 Localized Scleroderma 65 0.584
153
EPD006 Epidermolysis Bullosa Acquisita 48 0.584
154
BLL006 Bullous Pemphigoid 61 0.584
155
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.584
156
P SNS001 Sensorineural Hearing Loss 59 0.584
157
P FCL005 Focal Segmental Glomerulosclerosis 57 0.584
158
c ACT068 Acute Cystitis 61 0.584
159
IMP005 Impotence 52 0.584
160
PMP002 Pemphigoid Gestationis 38 0.584
161
P HYP086 Hypothyroidism 69 0.584
162
P HYD006 Hydrocephalus 61 0.584
163
HMP001 Hemopericardium 47 0.584
164
c MLG069 Malignant Hypertension 46 0.584
165
TRC008 Trachoma 53 0.584
166
P PRC012 Pericardial Effusion 50 0.584
167
P EPD016 Epidermolysis Bullosa 53 0.584
168
CNT047 Contact Dermatitis 57 0.584
169
RNL097 Renal Artery Disease 40 0.584
170
P PRP029 Porphyria 60 0.584
171
CHL068 Cholestasis 61 0.584
172
HDR003 Hidradenitis 50 0.584
173
LPT001 Leptospirosis 66 0.584
174
ENC005 Encephalomalacia 44 0.584
175
CLC006 Calcinosis 47 0.584
176
PRS030 Persistent Fetal Circulation Syndrome 49 0.584
177
HYP074 Hypersensitivity Vasculitis 53 0.584
178
P HRD221 Hereditary Nephrogenic Diabetes Insipidus 17 0.584
179
c CNT101 Central Congenital Hypothyroidism 36 0.584
180
EXF003 Exfoliative Dermatitis 22 0.584
181
HVY002 Heavy Metal Poisoning 22 0.584
182
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.578
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