Search results for Captopril

532 hits were found for Captopril

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.574
2
CNG034 Congestive Heart Failure 69 0.501
3
P RNV001 Renovascular Hypertension 48 0.454
4
P KDN018 Kidney Disease 72 0.287
5
P HRT032 Heart Disease 75 0.273
6
c ACT075 Acute Myocardial Infarction 57 0.254
7
c MCR113 Microvascular Complications of Diabetes 3 52 0.240
8
c MCR120 Microvascular Complications of Diabetes 7 47 0.239
9
c MCR130 Microvascular Complications of Diabetes 6 41 0.239
10
c MCR133 Microvascular Complications of Diabetes 4 41 0.239
11
P EXN002 Exanthem 57 0.205
12
P PLM037 Pulmonary Hypertension 67 0.181
13
c ACT071 Acute Kidney Failure 60 0.178
14
c DLT002 Dilated Cardiomyopathy 79 0.166
15
P NPH012 Nephrotic Syndrome 60 0.164
16
c MLG069 Malignant Hypertension 47 0.159
17
P RNL015 Renal Hypertension 47 0.159
18
P MYC007 Myocardial Infarction 70 0.153
19
GRN017 Granulocytopenia 44 0.150
20
c ATR087 Atrial Standstill 1 75 0.142
21
ANG054 Angina Pectoris 66 0.142
22
P NTR004 Neutropenia 63 0.142
23
LPP008 Lipoprotein Quantitative Trait Locus 62 0.142
24
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.139
25
P PMP001 Pemphigus 54 0.139
26
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.136
27
P SYS005 Systemic Scleroderma 68 0.129
28
HYP005 Hypokalemia 55 0.129
29
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.126
30
c CHR684 Chronic Kidney Disease 70 0.123
31
P VSC007 Vascular Disease 63 0.119
32
P MYC008 Myocarditis 59 0.116
33
PRT058 Pure Autonomic Failure 59 0.116
34
ART140 Arteries, Anomalies of 52 0.116
35
HYP540 Hypertension, Diastolic 40 0.116
36
LVR012 Liver Cirrhosis 62 0.112
37
P GLM007 Glomerulonephritis 57 0.112
38
END086 End Stage Renal Disease 51 0.112
39
P HYP098 Hypereosinophilic Syndrome 67 0.108
40
c DBT099 Diabetes Mellitus, Type I 65 0.108
41
c HYP836 Hypercholesterolemia, Familial, 1 73 0.104
42
ADN018 Adenoma 59 0.104
43
P ANG015 Angioedema 57 0.104
44
P MCR115 Microvascular Complications of Diabetes 5 66 0.100
45
CYS013 Cystinuria 63 0.100
46
c SCL052 Scleroderma, Familial Progressive 61 0.100
47
P LPS004 Lupus Erythematosus 61 0.100
48
ISC004 Ischemia 58 0.100
49
ALD013 Aldosterone-Producing Adenoma 39 0.100
50
CNN003 Conn's Syndrome 79 0.096
51
LPD008 Lipid Metabolism Disorder 62 0.096
52
HYP060 Hyperinsulinism 54 0.096
53
P ART018 Aortic Valve Insufficiency 49 0.096
54
c MTR002 Mitral Valve Insufficiency 48 0.096
55
CRD137 Cardiogenic Shock 47 0.096
56
c SYS001 Systemic Lupus Erythematosus 86 0.092
57
P RSP003 Respiratory Failure 74 0.087
58
PRP027 Peripheral Vascular Disease 71 0.087
59
P CRN300 Coronary Heart Disease 1 63 0.087
60
GLC003 Glucose Intolerance 54 0.087
61
RYN005 Raynaud Phenomenon 47 0.087
62
IDP033 Idiopathic Edema 44 0.087
63
RNL097 Renal Artery Disease 42 0.087
64
P FML187 Familial Hypertension 37 0.087
65
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.082
66
HYP056 Hypoglycemia 66 0.082
67
ATH013 Atherosclerosis Susceptibility 65 0.082
68
P DBT009 Diabetes Mellitus 64 0.082
69
PMP006 Pemphigus Vulgaris, Familial 57 0.082
70
INT007 Intermediate Coronary Syndrome 55 0.082
71
P MMB011 Membranous Nephropathy 50 0.082
72
IGG001 Iga Glomerulonephritis 48 0.082
73
FBR032 Fibromuscular Dysplasia 48 0.082
74
STR067 Stroke, Ischemic 81 0.077
75
c PRC016 Pre-Eclampsia 63 0.077
76
P VSC011 Vasculitis 62 0.077
77
DRM006 Dermatitis 61 0.077
78
LNG099 Lung Disease 60 0.077
79
NPH010 Nephrosclerosis 50 0.077
80
48X005 48,xyyy 39 0.077
81
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.077
82
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.071
83
P RHM011 Rheumatoid Arthritis 80 0.071
84
DFC004 Deficiency Anemia 70 0.071
85
P THR014 Thrombocytopenia 67 0.071
86
P CRD119 Cardiac Arrest 67 0.071
87
P HPT021 Hepatitis 67 0.071
88
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.071
89
c MCR129 Microvascular Complications of Diabetes 1 66 0.071
90
P PLM036 Pulmonary Fibrosis 65 0.071
91
P HML002 Hemolytic Anemia 63 0.071
92
P HYP750 Hypertriglyceridemia, Familial 62 0.071
93
HYP066 Hyperglycemia 61 0.071
94
INT002 Intermittent Claudication 61 0.071
95
c ACT027 Acute Pancreatitis 60 0.071
96
PLM010 Pulmonary Edema 54 0.071
97
c MCR112 Microvascular Complications of Diabetes 2 41 0.071
98
KPS004 Kaposi Sarcoma 75 0.065
99
GLB015 Glioblastoma Multiforme 75 0.065
100
c THR092 Thrombophilia Due to Thrombin Defect 73 0.065
101
ADL002 Adult Syndrome 70 0.065
102
P ART022 Arthritis 69 0.065
103
DPR016 Depression 63 0.065
104
P PNC044 Pancreatitis 61 0.065
105
HYD002 Hydronephrosis 60 0.065
106
PRT013 Portal Hypertension 59 0.065
107
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.065
108
HYP266 Hypoxia 57 0.065
109
P PYL005 Pyelonephritis 56 0.065
110
P NRP001 Neuropathy 56 0.065
111
PNC001 Pancytopenia 54 0.065
112
P MTR003 Mitral Valve Stenosis 50 0.065
113
INT067 Interstitial Nephritis 48 0.065
114
ANR004 Anuria 46 0.065
115
ACT003 Acute Kidney Tubular Necrosis 45 0.065
116
CYT002 Cytokine Deficiency 42 0.065
117
P HYP120 Hypoaldosteronism 36 0.065
118
EXF003 Exfoliative Dermatitis 27 0.065
119
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.065
120
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.058
121
P SRC025 Sarcoidosis 1 70 0.058
122
MYL005 Myelofibrosis 70 0.058
123
P LYM118 Lymphoma 68 0.058
124
P LKM002 Leukemia 68 0.058
125
BRK010 Burkitt Lymphoma 67 0.058
126
CRB039 Cerebrovascular Disease 67 0.058
127
c RHB024 Rhabdomyosarcoma 2 67 0.058
128
MYC006 Mycosis Fungoides 66 0.058
129
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.058
130
c WLM013 Wilms Tumor 1 65 0.058
131
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.058
132
MSC007 Muscle Hypertrophy 64 0.058
133
ATM095 Autoimmune Disease 62 0.058
134
ALL026 Allergic Hypersensitivity Disease 62 0.058
135
CHL068 Cholestasis 61 0.058
136
c WLM018 Wilms Tumor 5 61 0.058
137
P HMN010 Hemangioma 61 0.058
138
P MYL006 Myeloid Leukemia 60 0.058
139
P BCL017 B-Cell Lymphoma 58 0.058
140
P URT039 Urticaria 58 0.058
141
P CRD246 Cardiovascular System Disease 57 0.058
142
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.058
143
P DRR001 Diarrhea 55 0.058
144
HRT012 Heart Valve Disease 53 0.058
145
P ECL001 Eclampsia 50 0.058
146
c SVR005 Severe Pre-Eclampsia 50 0.058
147
47X002 47,xyy 49 0.058
148
CRN017 Coronary Thrombosis 47 0.058
149
SYN036 Syncope 45 0.058
150
PTY001 Pityriasis Rosea 44 0.058
151
CVD001 Covid-19 44 0.058
152
PMP004 Pemphigus Foliaceus 43 0.058
153
RST023 Resting Heart Rate, Variation in 41 0.058
154
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.058
155
P LNG032 Lung Cancer 98 0.050
156
P BRS047 Breast Cancer 97 0.050
157
MYL069 Myeloma, Multiple 85 0.050
158
c LKM061 Leukemia, Acute Myeloid 84 0.050
159
P LKM071 Leukemia, Chronic Lymphocytic 79 0.050
160
P APL001 Aplastic Anemia 74 0.050
161
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.050
162
P NRB001 Neuroblastoma 72 0.050
163
c LKM063 Leukemia, Chronic Myeloid 72 0.050
164
P PHC003 Pheochromocytoma 71 0.050
165
MYL009 Myelodysplastic Syndrome 70 0.050
166
MLT157 Multiple System Atrophy 1 70 0.050
167
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.050
168
LYM133 Lymphoma, Hodgkin, Classic 69 0.050
169
P LKM062 Leukemia, Acute Lymphoblastic 69 0.050
170
MNT001 Mantle Cell Lymphoma 69 0.050
171
P LVR013 Liver Disease 68 0.050
172
P PNM007 Pneumonia 68 0.050
173
P FLL037 Follicular Lymphoma 67 0.050
174
CHG001 Chagas Disease 66 0.050
175
c SML038 Small Cell Cancer of the Lung 65 0.050
176
c ART101 Aortic Valve Disease 2 65 0.050
177
P ADL010 Adult Respiratory Distress Syndrome 65 0.050
178
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.050
179
P RHB003 Rhabdomyosarcoma 63 0.050
180
ACT119 Acute Promyelocytic Leukemia 63 0.050
181
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.050
182
c SVR001 Severe Acute Respiratory Syndrome 62 0.050
183
BLL006 Bullous Pemphigoid 62 0.050
184
SZR001 Sezary's Disease 60 0.050
185
P TST021 Testicular Germ Cell Tumor 60 0.050
186
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.050
187
ANR040 Aneurysm 59 0.050
188
CRD132 Cardiac Conduction Defect 58 0.050
189
NWB001 Newborn Respiratory Distress Syndrome 58 0.050
190
c VSC019 Vesicoureteral Reflux 1 57 0.050
191
THR024 Thrombosis 57 0.050
192
PGM001 Pigmented Villonodular Synovitis 56 0.050
193
EMB004 Embryonal Carcinoma 56 0.050
194
AGN016 Aging 56 0.050
195
ADR008 Adrenal Adenoma 55 0.050
196
P DBT005 Diabetes Insipidus 55 0.050
197
HRY003 Hairy Cell Leukemia 55 0.050
198
PRP030 Purpura 54 0.050
199
P ALP008 Alopecia 54 0.050
200
HMS001 Hemosiderosis 54 0.050
201
LYM040 Lymphoblastic Lymphoma 54 0.050
202
P LCH002 Lichen Planus 53 0.050
203
FNG017 Fungal Infectious Disease 53 0.050
204
HMC014 Homocysteinemia 53 0.050
205
MRG003 Marginal Zone B-Cell Lymphoma 52 0.050
206
IMP005 Impotence 52 0.050
207
P TRT010 Teratoma 52 0.050
208
PNG002 Pain Agnosia 51 0.050
210
PLS009 Plasma Cell Neoplasm 51 0.050
211
ILS001 Ileus 51 0.050
212
P CPL006 Capillary Hemangioma 51 0.050
213
LNG031 Lung Benign Neoplasm 51 0.050
214
SPL004 Splenic Marginal Zone Lymphoma 51 0.050
215
c HNT004 Huntington Disease-Like 2 50 0.050
216
CRT013 Carotid Stenosis 50 0.050
217
c CPL013 Capillary Malformations, Congenital 50 0.050
218
HYP006 Hypertensive Heart Disease 49 0.050
219
c FLL041 Follicular Lymphoma 1 49 0.050
220
RYN001 Raynaud Disease 48 0.050
221
WTH001 Withdrawal Disorder 48 0.050
222
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.050
223
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.050
224
SXL003 Sexual Disorder 47 0.050
225
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.050
226
RNL077 Renal Fibrosis 47 0.050
227
PLS025 Plasmablastic Lymphoma 47 0.050
228
P CRC039 Coarctation of Aorta 47 0.050
229
CHR074 Choriocarcinoma 47 0.050
230
LYM019 Lymphosarcoma 46 0.050
231
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.050
232
ATN005 Autonomic Dysfunction 46 0.050
233
c ACT076 Acute Myocarditis 46 0.050
234
ADR040 Adrenal Gland Pheochromocytoma 46 0.050
235
GST010 Gestational Trophoblastic Neoplasm 46 0.050
236
OVR112 Ovarian Germ Cell Cancer 45 0.050
237
CHL149 Childhood Acute Myeloid Leukemia 44 0.050
238
P END039 Endodermal Sinus Tumor 44 0.050
239
PPL001 Papillary Adenoma 44 0.050
240
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.050
241
MTR010 Mature Teratoma 44 0.050
242
CRS005 Crest Syndrome 43 0.050
243
SMN007 Seminoma 43 0.050
244
P TST026 Testicular Germ Cell Cancer 43 0.050
245
c MLG081 Malignant Teratoma 43 0.050
246
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.050
247
PLM184 Pulmonary Arterial Hypertension Associated with Congenital Heart Disease 42 0.050
248
ANX004 Anoxia 40 0.050
249
KLD004 Keloid Disorder 40 0.050
250
TST018 Testicular Yolk Sac Tumor 39 0.050
251
P PRC031 Preeclampsia/eclampsia 1 38 0.050
252
OVR094 Ovarian Epithelial Cancer 38 0.050
253
c HNT011 Huntington Disease-Like 3 38 0.050
254
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.050
255
TRP005 Trophoblastic Neoplasm 38 0.050
256
c CHR098 Chronic Pyelonephritis 38 0.050
257
c WLM011 Wilms Tumor 6 37 0.050
258
PLY036 Polyembryoma 36 0.050
259
OVR051 Ovarian Endodermal Sinus Tumor 36 0.050
260
OVR050 Ovarian Embryonal Carcinoma 35 0.050
261
OVR015 Ovarian Mixed Germ Cell Neoplasm 35 0.050
262
TST043 Testicular Seminoma 35 0.050
263
GRM010 Germ Cells Tumors 34 0.050
264
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.050
265
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.050
266
IMM005 Immature Teratoma of Ovary 33 0.050
267
RFR002 Refractory Hairy Cell Leukemia 33 0.050
268
CHR076 Choriocarcinoma of the Testis 33 0.050
269
EMB006 Embryonal Testis Carcinoma 31 0.050
270
CHR075 Choriocarcinoma of Ovary 31 0.050
271
MXD032 Mixed Germ Cell Tumor 31 0.050
272
DRM005 Dermoid Cyst of Ovary 30 0.050
273
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.050
274
c TST046 Testicular Germ Cell Tumor 1 29 0.050
275
TRT017 Teratoma, Ovarian 29 0.050
276
MXD025 Mixed Germ Cell Cancer 28 0.050
277
TST020 Testis Seminoma 28 0.050
278
CLS052 Classic Hairy Cell Leukemia 27 0.050
279
CHL079 Children's Interstitial Lung Disease 26 0.050
280
MLG164 Malignant Epithelial Tumor of Ovary 26 0.050
281
P GLM040 Glioma Susceptibility 1 81 0.041
282
INS024 Insulin-Like Growth Factor I 79 0.041
283
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.041
284
AST005 Asthma 76 0.041
285
ART016 Aortic Aneurysm 69 0.041
286
CNN005 Connective Tissue Disease 68 0.041
287
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.041
288
ALC007 Alcohol Dependence 66 0.041
289
P ATR011 Atrial Fibrillation 66 0.041
290
c FML001 Familial Atrial Fibrillation 65 0.041
291
P ART005 Arteriovenous Malformation 65 0.041
292
SRC014 Sarcoma 65 0.041
293
PRT037 Pertussis 65 0.041
294
PRT036 Peritonitis 64 0.041
295
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.041
296
P PSR002 Psoriasis 62 0.041
297
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.041
298
P KDN017 Kidney Cancer 60 0.041
299
P VNT002 Ventricular Septal Defect 60 0.041
300
P CTR002 Cataract 60 0.041
301
P ALC033 Alcohol Use Disorder 58 0.041
302
CNT047 Contact Dermatitis 58 0.041
303
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.041
304
CNS004 Constipation 58 0.041
305
P PRP019 Peripheral Nervous System Disease 58 0.041
306
P RHN004 Rhinitis 57 0.041
307
P FCL005 Focal Segmental Glomerulosclerosis 57 0.041
308
SCH014 Schistosomiasis 57 0.041
309
BCT022 Bacterial Infectious Disease 56 0.041
310
P RST002 Restrictive Cardiomyopathy 56 0.041
311
c FML035 Familial Hyperlipidemia 55 0.041
312
NPH009 Nephrolithiasis 55 0.041
313
PRC013 Pericarditis 54 0.041
314
AMN001 Amenorrhea 54 0.041
315
PRS045 Prostatic Hypertrophy 53 0.041
316
RHM028 Rheumatic Heart Disease 53 0.041
317
P HML001 Hemolytic-Uremic Syndrome 53 0.041
318
SPN035 Spindle Cell Sarcoma 53 0.041
319
PRP080 Peripheral Artery Disease 53 0.041
320
PST011 Pustulosis of Palm and Sole 52 0.041
321
P BRT004 Bartter Disease 52 0.041
322
OCL069 Ocular Motor Apraxia 51 0.041
323
PRS021 Prostatic Adenoma 51 0.041
324
HPT014 Hepatorenal Syndrome 50 0.041
325
MTB004 Metabolic Acidosis 50 0.041
326
HRT011 Heart Septal Defect 50 0.041
327
PRS129 Prostatic Hyperplasia, Benign 49 0.041
328
SLD003 Sialadenitis 49 0.041
329
URM002 Uremia 49 0.041
330
SPL018 Splenomegaly 48 0.041
331
P MRC003 Mercury Poisoning 48 0.041
332
CRN027 Corneal Neovascularization 47 0.041
333
P CLL015 Collagen Disease 47 0.041
334
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.041
335
MYC005 Myocardial Stunning 46 0.041
336
URT010 Ureteral Obstruction 45 0.041
337
IMM003 Immunoglobulin Alpha Deficiency 45 0.041
338
ATN004 Autonomic Neuropathy 45 0.041
339
URT037 Urethral Stricture 43 0.041
340
c FML015 Familial Nephrotic Syndrome 41 0.041
341
RDN001 Reading Disorder 40 0.041
342
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.041
343
KLD003 Keloid Formation 38 0.041
344
GLM044 Glomerular Disease 37 0.041
345
THR123 Thrombotic Microangiopathy 36 0.041
346
LCH013 Lichen Planus Pemphigoides 34 0.041
347
PST092 Posttransplant Acute Limbic Encephalitis 29 0.041
348
MST020 Mast Cell Activation Syndrome 26 0.041
349
RRC029 Rare Cause of Hypertension 17 0.041
350
P PNC035 Pancreatic Cancer 84 0.029
351
IMM167 Immune Deficiency Disease 78 0.029
352
OST012 Osteoarthritis 78 0.029
353
P LNG064 Lung Cancer Susceptibility 3 78 0.029
354
SCK003 Sickle Cell Anemia 74 0.029
355
P SCH015 Schizophrenia 74 0.029
356
SVR004 Severe Combined Immunodeficiency 73 0.029
357
ANX010 Anxiety 73 0.029
358
P FML011 Familial Adenomatous Polyposis 72 0.029
359
P GRF003 Graft-Versus-Host Disease 72 0.029
360
c EXD008 Exudative Vitreoretinopathy 1 71 0.029
361
P EPL164 Epilepsy 71 0.029
362
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.029
363
P AMY004 Amyloidosis 70 0.029
364
DWN001 Down Syndrome 70 0.029
365
P HYP061 Hypertrophic Cardiomyopathy 70 0.029
366
P TTR001 Tetralogy of Fallot 70 0.029
367
SVR097 Severe Cutaneous Adverse Reaction 69 0.029
368
P SLP006 Sleep Apnea 69 0.029
369
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.029
370
BRN024 Bronchitis 68 0.029
371
ALL003 Allergic Rhinitis 67 0.029
372
P TRN020 Turner Syndrome 67 0.029
373
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.029
374
MSM014 Mismatch Repair Cancer Syndrome 65 0.029
375
P HRP006 Herpes Simplex 65 0.029
376
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.029
377
P ADN016 Adenocarcinoma 64 0.029
378
P GLM045 Glioma 63 0.029
379
P HYP069 Hyperparathyroidism 63 0.029
380
c ACT068 Acute Cystitis 63 0.029
381
ANR007 Anorexia Nervosa 63 0.029
382
P END044 Endometriosis 63 0.029
383
c GLC092 Glaucoma, Primary Open Angle 62 0.029
384
CLT003 Colitis 62 0.029
385
TKY002 Takayasu Arteritis 62 0.029
386
FTT001 Fatty Liver Disease 61 0.029
387
P ENC004 Encephalitis 61 0.029
388
SPN186 Spinal Cord Injury 60 0.029
389
DPH001 Diphtheria 60 0.029
390
P BNG030 Benign Ependymoma 60 0.029
391
CRD223 Cardiac Arrhythmia 60 0.029
392
INS001 Insulinoma 60 0.029
393
P GLY013 Glycogen Storage Disease 60 0.029
394
CHL014 Cholera 59 0.029
395
P SLP005 Sleep Disorder 59 0.029
396
PLM033 Pulmonary Embolism 59 0.029
397
PRN019 Perinatal Necrotizing Enterocolitis 59 0.029
398
GRD007 Grade Iii Astrocytoma 59 0.029
399
P HMN036 Hemangiopericytoma, Malignant 59 0.029
400
CYS010 Cystinosis 59 0.029
401
ERY003 Erythema Multiforme 58 0.029
402
P BNC003 Bone Cancer 58 0.029
403
MXD005 Mixed Connective Tissue Disease 58 0.029
404
P INF032 Infertility 57 0.029
405
P UVT001 Uveitis 57 0.029
406
IRN002 Iron Metabolism Disease 57 0.029
407
BRN056 Bronchopulmonary Dysplasia 57 0.029
408
P MYM013 Moyamoya Disease 1 57 0.029
409
P HDC001 Headache 57 0.029
410
DSS009 Disseminated Intravascular Coagulation 57 0.029
411
P PRN023 Prion Disease 57 0.029
412
APH001 Aphthous Stomatitis 57 0.029
413
CMM005 Common Cold 57 0.029
414
CHR177 Chromophobe Renal Cell Carcinoma 57 0.029
415
HMR039 Hemorrhage, Intracerebral 57 0.029
416
P PLY018 Polycythemia 56 0.029
417
P FBR017 Fibrosarcoma 56 0.029
418
c ACT134 Acute Liver Failure 56 0.029
419
DBL002 Double Outlet Right Ventricle 56 0.029
420
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.029
421
BRN004 Brain Edema 56 0.029
422
ATR057 Atrioventricular Block 55 0.029
423
MCN007 Meconium Aspiration Syndrome 55 0.029
424
MCL006 Macular Retinal Edema 55 0.029
425
c PRG126 Progressive Familial Heart Block 55 0.029
426
P MLN007 Male Infertility 55 0.029
427
P ANT006 Antiphospholipid Syndrome 55 0.029
428
P SBS003 Substance Abuse 55 0.029
429
JVN009 Juvenile Pilocytic Astrocytoma 55 0.029
430
URN010 Urinary Tract Obstruction 55 0.029
431
FCT004 Factor Xii Deficiency 55 0.029
432
BRN014 Bronchopneumonia 54 0.029
433
CLL010 Cellular Ependymoma 54 0.029
434
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.029
435
GSG001 Gas Gangrene 53 0.029
436
GST023 Gastric Ulcer 53 0.029
437
P RTN018 Retinal Disease 53 0.029
438
CHR073 Choreatic Disease 52 0.029
439
HRP009 Herpes Simplex Encephalitis 52 0.029
440
P DDN001 Duodenal Ulcer 52 0.029
441
P ACT105 Acute Mountain Sickness 52 0.029
442
HYP014 Hyperuricemia 52 0.029
443
ART074 Aortic Dissection 52 0.029
444
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.029
445
TLN003 Telangiectasis 52 0.029
446
KRT009 Keratosis 51 0.029
447
ENT011 Enterocolitis 51 0.029
448
P AST007 Astrocytoma 51 0.029
449
HYP074 Hypersensitivity Vasculitis 51 0.029
450
CRV040 Cervix Carcinoma 51 0.029
451
P CHL066 Cholangitis 51 0.029
452
PLR008 Pleurisy 50 0.029
453
RTN003 Retinal Ischemia 50 0.029
454
BLP005 Blepharitis 50 0.029
455
CRN030 Coronary Stenosis 50 0.029
456
STM007 Stomatitis 50 0.029
457
NTR046 Neutrophil Migration 50 0.029
458
P OTS001 Otosclerosis 49 0.029
459
P IGN003 Iga Nephropathy 1 49 0.029
460
SYS003 Systolic Heart Failure 49 0.029
461
LFT001 Left Bundle Branch Hemiblock 49 0.029
462
P OPN001 Open-Angle Glaucoma 49 0.029
463
BNR002 Bone Resorption Disease 48 0.029
464
CLC006 Calcinosis 48 0.029
465
DRG013 Drug-Induced Lupus Erythematosus 48 0.029
466
ART004 Aortic Atherosclerosis 47 0.029
467
HLX001 Helix Syndrome 47 0.029
468
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.029
469
PRD004 Prediabetes Syndrome 47 0.029
470
P HMN032 Human Herpesvirus 8 47 0.029
471
P ERY008 Erythromelalgia 47 0.029
472
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.029
473
TST014 Testicular Cancer 46 0.029
474
BCK003 Background Diabetic Retinopathy 46 0.029
475
c ACQ010 Acquired Polycythemia 46 0.029
476
c BRT042 Bartter Syndrome, Type 3 46 0.029
477
PLL012 Pollen Allergy 46 0.029
478
LKS001 Leukostasis 46 0.029
479
GLL048 Glial Tumor 45 0.029
480
PPL018 Papillary Adenocarcinoma 45 0.029
481
HPT004 Hepatic Coma 45 0.029
482
DST006 Diastolic Heart Failure 45 0.029
483
CRB004 Cerebral Artery Occlusion 45 0.029
484
URL001 Urolithiasis 45 0.029
485
HMP009 Haemophilus Influenzae 43 0.029
486
P PRT026 Parotitis 42 0.029
487
IDP091 Idiopathic Nephrotic Syndrome 42 0.029
488
c PST041 Posterior Urethral Valves 41 0.029
489
DBT002 Diabetic Autonomic Neuropathy 41 0.029
490
DFF003 Diffuse Scleroderma 41 0.029
491
P DYS021 Dysautonomia 39 0.029
492
c ACT079 Acute Proliferative Glomerulonephritis 39 0.029
493
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.029
494
ALL014 Allergic Encephalomyelitis 38 0.029
495
SCR039 Scorpion Envenomation 38 0.029
496
TYM001 Tympanosclerosis 38 0.029
497
ADR048 Adrenal Hyperplasia, Congenital, Due to 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency 37 0.029
498
CRT012 Cortical Blindness 37 0.029
499
ACT040 Acute Poststreptococcal Glomerulonephritis 36 0.029
500
HYP114 Hypertensive Nephropathy 36 0.029
501
DFF021 Diffuse Mesangial Sclerosis 35 0.029
502
OLG006 Oligoastrocytoma 35 0.029
503
c ATM022 Autoimmune Myocarditis 35 0.029
504
CHR178 Chromosomal Triplication 35 0.029
505
BLD009 Bladder Neck Obstruction 35 0.029
506
c MYC058 Myocardial Infarction 2 34 0.029
507
PPL052 Papillomatosis, Confluent and Reticulated 33 0.029
508
c CHR064 Chronic Monocytic Leukemia 33 0.029
509
INF013 Inferior Myocardial Infarction 33 0.029
510
PRN007 Perinephritis 33 0.029
511
c MLG003 Malignant Renovascular Hypertension 32 0.029
512
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.029
513
KDN013 Kidney Hypertrophy 32 0.029
514
FLL019 Follicular Mucinosis 31 0.029
515
DRF001 Dirofilariasis 31 0.029
516
MLT116 Multiple System Atrophy, Parkinsonian Type 30 0.029
517
ERY066 Erythema Multiforme Major 30 0.029
518
ACT228 Acute Radiation Syndrome 29 0.029
519
PMP008 Pemphigus Vegetans 27 0.029
520
DFF015 Diffuse Glomerulonephritis 26 0.029
521
SPC030 Specific Language Disorder 26 0.029
522
TXC010 Toxic Myocarditis 26 0.029
523
STN013 Stenotrophomonas Maltophilia Infection 25 0.029
524
VSC052 Vasculitis, Lymphocytic, Nodular 25 0.029
525
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.029
526
PLM061 Pulmonary Edema of Mountaineers 25 0.029
527
DPS001 Dipsogenic Diabetes Insipidus 23 0.029
528
c MLG039 Malignant Essential Hypertension 22 0.029
529
c IGN002 Iga Nephropathy 2 20 0.029
530
ATR089 Atrioventricular Dissociation 20 0.029
531
CNG116 Congenital Nephrotic Syndrome Finnish Type 18 0.029
532
SPR072 Superficial Pemphigus 17 0.029
Content
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