Search results for Furosemide

547 hits were found for Furosemide

# Family MCID Name MIFTS Score
1
P ANT061 Antenatal Bartter Syndrome 37 4.142
2
CNG034 Congestive Heart Failure 69 0.535
3
P HRT032 Heart Disease 75 0.410
4
P KDN018 Kidney Disease 72 0.397
5
c ACT071 Acute Kidney Failure 60 0.308
6
HYP005 Hypokalemia 55 0.276
7
c HYP595 Hypertension, Essential 84 0.264
8
LVR012 Liver Cirrhosis 62 0.237
9
P NPH012 Nephrotic Syndrome 60 0.232
10
PLM010 Pulmonary Edema 54 0.213
11
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.196
12
c CHR684 Chronic Kidney Disease 70 0.182
13
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.178
14
P GLM007 Glomerulonephritis 57 0.168
15
BRN056 Bronchopulmonary Dysplasia 57 0.165
16
NPH003 Nephrocalcinosis 51 0.155
17
P LVR013 Liver Disease 68 0.143
18
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.140
19
48X005 48,xyyy 39 0.140
20
P RNL007 Renal Tubular Acidosis 51 0.137
21
P PTN014 Patent Ductus Arteriosus 1 60 0.124
22
END086 End Stage Renal Disease 51 0.124
23
P DBT005 Diabetes Insipidus 55 0.117
24
IDP033 Idiopathic Edema 44 0.117
25
P RSP003 Respiratory Failure 74 0.113
26
c PRC016 Pre-Eclampsia 63 0.113
27
URM002 Uremia 49 0.113
28
LNG099 Lung Disease 60 0.109
29
c ACT075 Acute Myocardial Infarction 57 0.109
30
P HYP069 Hyperparathyroidism 63 0.105
31
HYD002 Hydronephrosis 60 0.105
32
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.105
33
P DST107 Distal Renal Tubular Acidosis 42 0.105
34
AST005 Asthma 76 0.101
35
P ENC018 Encephalopathy 61 0.101
36
BRN002 Bronchiolitis 59 0.101
37
P RNV001 Renovascular Hypertension 48 0.101
38
HPT019 Hepatic Encephalopathy 60 0.097
39
P SNS001 Sensorineural Hearing Loss 60 0.097
40
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.097
41
CRD137 Cardiogenic Shock 47 0.097
42
HPT004 Hepatic Coma 45 0.097
43
c BRN108 Branchiootic Syndrome 1 62 0.092
44
MNR012 Meniere Disease 57 0.092
45
NPH009 Nephrolithiasis 55 0.092
46
c MCR113 Microvascular Complications of Diabetes 3 52 0.092
47
c SCN007 Secondary Hyperparathyroidism 51 0.092
48
P ECL001 Eclampsia 50 0.092
49
c MCR120 Microvascular Complications of Diabetes 7 47 0.092
50
P BRB001 Beriberi 46 0.092
51
ATX019 Ataxia with Vitamin E Deficiency 42 0.092
52
c MCR130 Microvascular Complications of Diabetes 6 41 0.092
53
c MCR133 Microvascular Complications of Diabetes 4 41 0.092
54
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.088
55
c ATR087 Atrial Standstill 1 75 0.088
56
P PLM037 Pulmonary Hypertension 67 0.088
57
ALL026 Allergic Hypersensitivity Disease 62 0.088
58
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.088
59
BRN004 Brain Edema 56 0.088
60
INT075 Intracranial Hypertension 53 0.088
61
MTB004 Metabolic Acidosis 50 0.088
62
URT010 Ureteral Obstruction 45 0.088
63
LPT014 Leptin Deficiency or Dysfunction 74 0.083
64
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.083
65
MSC007 Muscle Hypertrophy 64 0.083
66
BLL006 Bullous Pemphigoid 62 0.083
67
P RHN004 Rhinitis 57 0.083
68
P PYL005 Pyelonephritis 56 0.083
69
c SVR005 Severe Pre-Eclampsia 50 0.083
70
SYS003 Systolic Heart Failure 49 0.083
71
c MTR002 Mitral Valve Insufficiency 48 0.083
72
ACT003 Acute Kidney Tubular Necrosis 45 0.083
73
c DLT002 Dilated Cardiomyopathy 79 0.077
74
P MYC007 Myocardial Infarction 70 0.077
75
ADL002 Adult Syndrome 70 0.077
76
c RHB024 Rhabdomyosarcoma 2 67 0.077
77
P DBT009 Diabetes Mellitus 64 0.077
78
LPD008 Lipid Metabolism Disorder 62 0.077
79
ISC004 Ischemia 58 0.077
80
OCL069 Ocular Motor Apraxia 51 0.077
81
c INF145 Infantile Liver Failure Syndrome 1 50 0.077
82
ANR004 Anuria 46 0.077
83
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.077
84
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.072
85
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.072
86
P ATR011 Atrial Fibrillation 66 0.072
87
NTR005 Nutritional Deficiency Disease 62 0.072
88
HYP066 Hyperglycemia 61 0.072
89
P PNC044 Pancreatitis 61 0.072
90
P BND020 Bone Disease 59 0.072
91
NWB001 Newborn Respiratory Distress Syndrome 58 0.072
92
P FCL005 Focal Segmental Glomerulosclerosis 57 0.072
93
URN010 Urinary Tract Obstruction 55 0.072
94
GLC003 Glucose Intolerance 54 0.072
95
ANL018 Analbuminemia 54 0.072
96
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.072
97
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.072
98
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.072
99
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.072
100
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.072
101
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.072
102
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.072
103
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.072
104
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.072
105
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.072
106
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.072
107
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.072
108
DFC004 Deficiency Anemia 70 0.065
109
ALL003 Allergic Rhinitis 67 0.065
110
c FML001 Familial Atrial Fibrillation 65 0.065
111
P ADL010 Adult Respiratory Distress Syndrome 65 0.065
112
GT001 Gout 64 0.065
113
TXC005 Toxic Shock Syndrome 62 0.065
114
c ACT027 Acute Pancreatitis 60 0.065
115
P CYS018 Cystitis 59 0.065
116
ADN018 Adenoma 59 0.065
117
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.065
118
ERY003 Erythema Multiforme 58 0.065
119
PTH003 Pathologic Nystagmus 52 0.065
120
P RNL015 Renal Hypertension 47 0.065
121
P PRC031 Preeclampsia/eclampsia 1 38 0.065
122
P HPT023 Hepatocellular Carcinoma 100 0.058
123
STR067 Stroke, Ischemic 81 0.058
124
CNN003 Conn's Syndrome 79 0.058
125
RCK004 Rickets 68 0.058
126
P HPT021 Hepatitis 67 0.058
127
CRB039 Cerebrovascular Disease 67 0.058
128
P TRN020 Turner Syndrome 67 0.058
129
P CRN300 Coronary Heart Disease 1 63 0.058
130
c ACT068 Acute Cystitis 63 0.058
131
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.058
132
LPP008 Lipoprotein Quantitative Trait Locus 62 0.058
133
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.058
134
PRT013 Portal Hypertension 59 0.058
135
GST045 Gastroenteritis 59 0.058
136
GLS018 Glass Syndrome 57 0.058
137
CMM005 Common Cold 57 0.058
138
ALC009 Alcoholic Liver Cirrhosis 53 0.058
139
HPT014 Hepatorenal Syndrome 50 0.058
140
CHL004 Cholelithiasis 49 0.058
141
P CRC039 Coarctation of Aorta 47 0.058
142
LPD004 Lipoid Nephrosis 46 0.058
143
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.058
144
c PRM038 Primary Agammaglobulinemia 44 0.058
145
P LBY004 Labyrinthitis 42 0.058
146
CHL079 Children's Interstitial Lung Disease 26 0.058
147
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.058
148
CYS001 Cystic Fibrosis 81 0.051
149
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.051
150
BRN028 Brain Cancer 74 0.051
151
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.051
152
DWN001 Down Syndrome 70 0.051
153
SVR097 Severe Cutaneous Adverse Reaction 69 0.051
154
P LKM002 Leukemia 68 0.051
155
P INF038 Influenza 68 0.051
156
P THR014 Thrombocytopenia 67 0.051
157
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.051
158
P HYP098 Hypereosinophilic Syndrome 67 0.051
159
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.051
160
P MCR115 Microvascular Complications of Diabetes 5 66 0.051
161
c MCR129 Microvascular Complications of Diabetes 1 66 0.051
162
P HYD006 Hydrocephalus 66 0.051
163
P VSC007 Vascular Disease 63 0.051
164
c FNC043 Fanconi Anemia, Complementation Group E 62 0.051
165
c HPT001 Hepatitis C 62 0.051
166
P VSC011 Vasculitis 62 0.051
167
ATM095 Autoimmune Disease 62 0.051
168
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.051
169
FTT001 Fatty Liver Disease 61 0.051
170
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.051
171
P MYC008 Myocarditis 59 0.051
172
THY029 Thyroid Carcinoma 59 0.051
173
PLM033 Pulmonary Embolism 59 0.051
174
VSL002 Visual Epilepsy 59 0.051
175
P URT039 Urticaria 58 0.051
176
P MTR012 Mitral Valve Disease 58 0.051
177
IRN002 Iron Metabolism Disease 57 0.051
178
P EXN002 Exanthem 57 0.051
179
THR024 Thrombosis 57 0.051
180
P CRD246 Cardiovascular System Disease 57 0.051
181
P ANG015 Angioedema 57 0.051
182
PNM008 Pneumothorax 56 0.051
183
BCT022 Bacterial Infectious Disease 56 0.051
184
P SZR006 Seizure Disorder 56 0.051
185
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.051
186
NNL006 Non-Alcoholic Steatohepatitis 54 0.051
187
GST009 Gastroschisis 53 0.051
188
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.051
189
P ACT008 Actinic Keratosis 53 0.051
190
c GLL024 Gallbladder Disease 1 53 0.051
191
P BRT004 Bartter Disease 52 0.051
192
HYP014 Hyperuricemia 52 0.051
193
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.051
194
KRT009 Keratosis 51 0.051
195
PRT018 Portal Vein Thrombosis 50 0.051
196
INP001 Inappropriate Adh Syndrome 49 0.051
197
P CMP008 Compartment Syndrome 49 0.051
198
HDN002 Head Injury 46 0.051
199
HMR023 Hemorrhagic Cystitis 45 0.051
200
DST006 Diastolic Heart Failure 45 0.051
201
CYT002 Cytokine Deficiency 42 0.051
203
49X006 49, Xxxxy Syndrome 41 0.051
204
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.051
205
c MCR112 Microvascular Complications of Diabetes 2 41 0.051
206
ALD013 Aldosterone-Producing Adenoma 39 0.051
207
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.051
208
ABD010 Abdominal Wall Defect 36 0.051
209
c ATM022 Autoimmune Myocarditis 35 0.051
210
P VSC018 Visceral Steatosis 33 0.051
211
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.051
212
ERY066 Erythema Multiforme Major 30 0.051
213
c SLV028 Silver-Russell Syndrome 3 28 0.051
214
CYT018 Cytochrome P450 2d6 Variant 27 0.051
215
MYL069 Myeloma, Multiple 85 0.041
216
c LKM061 Leukemia, Acute Myeloid 84 0.041
217
P GST053 Gastric Cancer 83 0.041
218
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.041
219
P BLD134 Bladder Cancer 79 0.041
220
P SCH015 Schizophrenia 74 0.041
221
c HYP836 Hypercholesterolemia, Familial, 1 73 0.041
222
c HPT073 Hepatitis C Virus 72 0.041
223
P PHC003 Pheochromocytoma 71 0.041
224
ACR007 Acromegaly 71 0.041
225
BRN024 Bronchitis 68 0.041
226
P CRD119 Cardiac Arrest 67 0.041
227
c MGR028 Migraine with or Without Aura 1 67 0.041
228
LPT001 Leptospirosis 66 0.041
229
ANG054 Angina Pectoris 66 0.041
230
PRT036 Peritonitis 64 0.041
231
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.041
232
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.041
233
c SVR001 Severe Acute Respiratory Syndrome 62 0.041
234
P HYP750 Hypertriglyceridemia, Familial 62 0.041
235
CHL068 Cholestasis 61 0.041
236
P MYL006 Myeloid Leukemia 60 0.041
237
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.041
238
PRT058 Pure Autonomic Failure 59 0.041
239
P SYP003 Syphilis 58 0.041
240
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.041
241
CNS004 Constipation 58 0.041
242
BLR008 Bilirubin Metabolic Disorder 57 0.041
243
HYP266 Hypoxia 57 0.041
244
ALL006 Allergic Asthma 56 0.041
245
AGN016 Aging 56 0.041
246
ATR057 Atrioventricular Block 55 0.041
247
P DRR001 Diarrhea 55 0.041
248
ANG005 Anogenital Venereal Wart 55 0.041
249
P RST001 Restless Legs Syndrome 54 0.041
250
PRS045 Prostatic Hypertrophy 53 0.041
251
P HMR003 Hemorrhagic Disease 53 0.041
252
P ACT105 Acute Mountain Sickness 52 0.041
253
HYP081 Hypolipoproteinemia 51 0.041
254
PRT029 Parathyroid Adenoma 50 0.041
255
P MTR003 Mitral Valve Stenosis 50 0.041
256
NPH010 Nephrosclerosis 50 0.041
257
HYP017 Hypophosphatemia 50 0.041
258
47X002 47,xyy 49 0.041
259
VTM033 Vitamin K Deficiency Bleeding 48 0.041
260
INT067 Interstitial Nephritis 48 0.041
261
HYP025 Hyperphosphatemia 48 0.041
262
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.041
263
KRT013 Keratolytic Winter Erythema 46 0.041
264
ADR040 Adrenal Gland Pheochromocytoma 46 0.041
265
CRN019 Coronary Artery Vasospasm 46 0.041
266
c ACT042 Acute Pyelonephritis 46 0.041
267
SYN036 Syncope 45 0.041
268
URL001 Urolithiasis 45 0.041
269
c HYP272 Hypercholesterolemia, Familial, 3 44 0.041
270
VLV044 Vulvar Intraepithelial Neoplasia 44 0.041
271
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.041
272
ACT088 Acute Insulin Response 41 0.041
273
PST053 Postherpetic Neuralgia 40 0.041
274
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.041
275
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.041
276
c CHR098 Chronic Pyelonephritis 38 0.041
277
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.041
278
HRN029 Hearing Loss, Noise-Induced 37 0.041
279
ACT040 Acute Poststreptococcal Glomerulonephritis 36 0.041
280
c RST012 Restless Legs Syndrome 1 34 0.041
281
c CHR064 Chronic Monocytic Leukemia 33 0.041
282
GRN009 Granulomatous Hepatitis 33 0.041
283
INF013 Inferior Myocardial Infarction 33 0.041
284
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.041
285
c HRD219 Hereditary Distal Renal Tubular Acidosis 27 0.041
286
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.041
287
CRR012 Cirrhotic Cardiomyopathy 24 0.041
288
P CLR023 Colorectal Cancer 99 0.029
289
P LNG032 Lung Cancer 98 0.029
290
P PRS040 Prostate Cancer 97 0.029
291
P BRS047 Breast Cancer 97 0.029
292
ESP021 Esophageal Cancer 90 0.029
293
P OVR042 Ovarian Cancer 88 0.029
294
P PNC035 Pancreatic Cancer 84 0.029
295
INS024 Insulin-Like Growth Factor I 79 0.029
296
P PRK057 Parkinson Disease, Late-Onset 78 0.029
297
CRV035 Cervical Cancer 76 0.029
298
c ART115 Aortic Valve Disease 1 75 0.029
299
P OST002 Osteoporosis 74 0.029
300
c THR092 Thrombophilia Due to Thrombin Defect 73 0.029
301
P CNR004 Cone-Rod Dystrophy 2 73 0.029
302
P NRB001 Neuroblastoma 72 0.029
303
P GRF003 Graft-Versus-Host Disease 72 0.029
304
P SRC025 Sarcoidosis 1 70 0.029
305
P AMY004 Amyloidosis 70 0.029
306
GST040 Gastric Adenocarcinoma 70 0.029
307
MYL009 Myelodysplastic Syndrome 70 0.029
308
MYL005 Myelofibrosis 70 0.029
309
P TTR001 Tetralogy of Fallot 70 0.029
310
P SLP006 Sleep Apnea 69 0.029
311
LYM133 Lymphoma, Hodgkin, Classic 69 0.029
312
P HYP086 Hypothyroidism 69 0.029
313
P LYM118 Lymphoma 68 0.029
314
P CRN037 Craniosynostosis 68 0.029
315
P PNM007 Pneumonia 68 0.029
316
P MYC084 Mycobacterium Tuberculosis 1 68 0.029
317
P PRP003 Porphyria Cutanea Tarda 67 0.029
318
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.029
319
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.029
320
HYP056 Hypoglycemia 66 0.029
321
P MNN013 Meningitis 66 0.029
322
GTL001 Gitelman Syndrome 65 0.029
323
P CNJ013 Conjunctivitis 65 0.029
324
c ART101 Aortic Valve Disease 2 65 0.029
325
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.029
326
CHY002 Chylomicron Retention Disease 65 0.029
327
ATH013 Atherosclerosis Susceptibility 65 0.029
328
c DBT099 Diabetes Mellitus, Type I 65 0.029
329
APN008 Apnea, Obstructive Sleep 64 0.029
330
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.029
331
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.029
332
P ADN016 Adenocarcinoma 64 0.029
333
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.029
334
OST017 Osteomyelitis 64 0.029
335
c DPH024 Diaphragmatic Hernia, Congenital 63 0.029
336
LSH001 Leishmaniasis 63 0.029
337
P GLM045 Glioma 63 0.029
338
P NTR004 Neutropenia 63 0.029
339
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.029
340
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.029
341
TYP007 Typhoid Fever 63 0.029
342
SKN016 Skin Disease 63 0.029
343
TRN015 Transient Cerebral Ischemia 63 0.029
344
ANR007 Anorexia Nervosa 63 0.029
345
DPR016 Depression 63 0.029
346
c ALP101 Alpha-Thalassemia 62 0.029
347
HMT002 Hematologic Cancer 62 0.029
348
P ORT004 Orthostatic Intolerance 62 0.029
349
CTN007 Cutaneous Leishmaniasis 62 0.029
350
P PRP029 Porphyria 62 0.029
351
INT002 Intermittent Claudication 61 0.029
352
RTN017 Retinal Detachment 61 0.029
353
APP008 Appendicitis 61 0.029
354
SPN186 Spinal Cord Injury 60 0.029
355
HRP004 Herpes Zoster 60 0.029
356
PNM010 Pneumothorax, Primary Spontaneous 60 0.029
357
P TST021 Testicular Germ Cell Tumor 60 0.029
358
P SCL018 Scoliosis 60 0.029
359
VRC005 Varicose Veins 60 0.029
360
STT001 Status Epilepticus 60 0.029
361
P THL005 Thalassemia 60 0.029
362
CHL014 Cholera 59 0.029
363
c DNG003 Dengue Disease 59 0.029
364
ANR040 Aneurysm 59 0.029
365
P HYP726 Hypercalcemia, Infantile, 1 58 0.029
366
CRD132 Cardiac Conduction Defect 58 0.029
367
P ALC033 Alcohol Use Disorder 58 0.029
368
c PRM005 Primary Hyperparathyroidism 58 0.029
369
P MMP001 Mumps 58 0.029
370
APP015 Apparent Mineralocorticoid Excess 58 0.029
371
c CHR417 Chronic Graft Versus Host Disease 57 0.029
372
CHL067 Cholecystitis 57 0.029
373
c VSC019 Vesicoureteral Reflux 1 57 0.029
374
DSS009 Disseminated Intravascular Coagulation 57 0.029
375
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.029
376
INT303 Intracranial Hypertension, Idiopathic 57 0.029
377
PGM001 Pigmented Villonodular Synovitis 56 0.029
378
ERY051 Erythroleukemia, Familial 56 0.029
379
ACS001 Acoustic Neuroma 56 0.029
380
EMB004 Embryonal Carcinoma 56 0.029
381
INT030 Intracranial Aneurysm 56 0.029
382
MCS002 Mucositis 56 0.029
383
MCN007 Meconium Aspiration Syndrome 55 0.029
384
MCL006 Macular Retinal Edema 55 0.029
385
NRG002 Neurogenic Bladder 55 0.029
386
PLV003 Pelvic Inflammatory Disease 55 0.029
387
MMB001 Membranoproliferative Glomerulonephritis 55 0.029
388
P VNS003 Venous Insufficiency 55 0.029
389
P PRK001 Porokeratosis 55 0.029
390
INT007 Intermediate Coronary Syndrome 55 0.029
391
PRP030 Purpura 54 0.029
392
MNN032 Meningococcal Meningitis 54 0.029
393
P ALP008 Alopecia 54 0.029
394
BRN014 Bronchopneumonia 54 0.029
395
P ART021 Arteriosclerosis 54 0.029
396
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.029
397
RHM028 Rheumatic Heart Disease 53 0.029
398
HRT012 Heart Valve Disease 53 0.029
399
P INT068 Intestinal Disease 53 0.029
400
OST011 Osteomalacia 52 0.029
401
P SML001 Small Cell Carcinoma 52 0.029
402
P DDN001 Duodenal Ulcer 52 0.029
403
IMP005 Impotence 52 0.029
404
ART140 Arteries, Anomalies of 52 0.029
405
DYS015 Dysentery 52 0.029
406
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.029
407
ART074 Aortic Dissection 52 0.029
408
c ACT135 Acute Graft Versus Host Disease 52 0.029
409
P TRT010 Teratoma 52 0.029
410
PNG002 Pain Agnosia 51 0.029
411
OLG003 Oligohydramnios 51 0.029
412
PRS021 Prostatic Adenoma 51 0.029
413
PLS009 Plasma Cell Neoplasm 51 0.029
414
c ART120 Arthrogryposis, Distal, Type 3 51 0.029
415
MYL020 Myelomeningocele 51 0.029
416
TRM010 Traumatic Brain Injury 51 0.029
417
NRM004 Neuroma 51 0.029
418
HYP781 Hypoascorbemia 51 0.029
419
P CHL066 Cholangitis 51 0.029
420
PLR007 Pleural Empyema 50 0.029
421
P FNC004 Fanconi Syndrome 50 0.029
422
ALL009 Allergic Conjunctivitis 50 0.029
423
P TMP001 Temporal Lobe Epilepsy 50 0.029
424
PPL021 Papilledema 49 0.029
425
VLV047 Volvulus of Midgut 49 0.029
426
GYN001 Gynecomastia 49 0.029
427
PRS129 Prostatic Hyperplasia, Benign 49 0.029
428
BRN071 Brain Injury 49 0.029
429
ADR016 Adrenal Cortical Carcinoma 48 0.029
430
ADT003 Auditory System Disease 48 0.029
431
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.029
432
CLC006 Calcinosis 48 0.029
433
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.029
434
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.029
435
FBR032 Fibromuscular Dysplasia 48 0.029
436
c HYD064 Hydrocephalus, Congenital, 1 48 0.029
437
GRM005 Germ Cell Cancer 47 0.029
438
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.029
439
c MLG069 Malignant Hypertension 47 0.029
440
P PRR002 Pure Red-Cell Aplasia 47 0.029
441
RNL077 Renal Fibrosis 47 0.029
442
WRN003 Wernicke Encephalopathy 47 0.029
443
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.029
444
CNT033 Central Nervous System Cancer 47 0.029
445
CHR074 Choriocarcinoma 47 0.029
446
LYM019 Lymphosarcoma 46 0.029
447
TST014 Testicular Cancer 46 0.029
448
UMB002 Umbilical Hernia 46 0.029
449
PLY012 Polyhydramnios 46 0.029
450
MGC001 Megacolon 46 0.029
451
c BRT050 Bartter Syndrome, Type 2, Antenatal 46 0.029
452
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.029
453
GLL048 Glial Tumor 45 0.029
454
c TRC022 Tricuspid Valve Insufficiency 45 0.029
455
PLR022 Pleural Disease 45 0.029
456
SYN005 Synostosis 45 0.029
457
P PRD021 Periodic Paralysis 45 0.029
458
OVR112 Ovarian Germ Cell Cancer 45 0.029
459
SPS057 Spasticity 45 0.029
460
P PSD003 Pseudohypoaldosteronism 44 0.029
461
GRN017 Granulocytopenia 44 0.029
462
ART012 Aortitis 44 0.029
463
P END039 Endodermal Sinus Tumor 44 0.029
464
ACN001 Acinar Cell Carcinoma 44 0.029
465
PRT035 Peritoneum Cancer 44 0.029
466
c ORT011 Orthostatic Hypotension 1 44 0.029
467
P BCT020 Bacteremia 2 44 0.029
468
CVD001 Covid-19 44 0.029
469
P MYG005 Myoglobinuria 44 0.029
470
SMN007 Seminoma 43 0.029
471
P TST026 Testicular Germ Cell Cancer 43 0.029
472
MYX004 Myxedema 43 0.029
473
BNM001 Bone Marrow Cancer 43 0.029
474
DVR002 Diverticulitis 43 0.029
475
RDC006 Red Cell Aplasia 43 0.029
476
LWC001 Low Compliance Bladder 43 0.029
477
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.029
478
IDP073 Idiopathic Hypercalciuria 43 0.029
479
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.029
480
TRP009 Triple X Syndrome 42 0.029
481
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.029
482
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.029
483
IDP091 Idiopathic Nephrotic Syndrome 42 0.029
484
URT031 Ureteral Disease 41 0.029
485
c PST041 Posterior Urethral Valves 41 0.029
486
P KLZ004 Kala-Azar 1 41 0.029
487
RST023 Resting Heart Rate, Variation in 41 0.029
488
PRS063 Paresthesia 41 0.029
489
VST004 Vestibular Disease 41 0.029
490
RDN001 Reading Disorder 40 0.029
491
CRN322 Coronavirus Infectious Disease 40 0.029
492
P LTH003 Lethal Congenital Contracture Syndrome 40 0.029
493
ANX004 Anoxia 40 0.029
494
P FNC034 Fanconi Renotubular Syndrome 2 40 0.029
495
RTR011 Retroperitoneal Fibrosis 40 0.029
496
ADJ001 Adjustment Disorder 40 0.029
497
UTR043 Uterine Sarcoma 39 0.029
498
ENT001 Enterocele 39 0.029
499
ADR004 Adrenal Cortical Adenocarcinoma 39 0.029
500
c PLM022 Pulmonary Valve Insufficiency 39 0.029
501
TST018 Testicular Yolk Sac Tumor 39 0.029
502
c ACT079 Acute Proliferative Glomerulonephritis 39 0.029
503
NTR042 Neutrophilic Dermatosis, Acute Febrile 38 0.029
504
SWL001 Swallowing Disorders 38 0.029
505
TXC001 Toxic Megacolon 38 0.029
506
P FML187 Familial Hypertension 37 0.029
507
P HYP120 Hypoaldosteronism 36 0.029
508
HYP114 Hypertensive Nephropathy 36 0.029
509
OVR015 Ovarian Mixed Germ Cell Neoplasm 35 0.029
510
TST043 Testicular Seminoma 35 0.029
511
INT003 Intracranial Hypotension 35 0.029
512
GRM010 Germ Cells Tumors 34 0.029
513
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.029
514
PPL052 Papillomatosis, Confluent and Reticulated 33 0.029
515
CHR076 Choriocarcinoma of the Testis 33 0.029
516
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.029
517
EXT025 Extragonadal Germ Cell Cancer 32 0.029
518
KDN013 Kidney Hypertrophy 32 0.029
519
HRD218 Hereditary Stomatocytosis 32 0.029
520
DRF001 Dirofilariasis 31 0.029
521
INF021 Infant Gynecomastia 31 0.029
522
EMB006 Embryonal Testis Carcinoma 31 0.029
523
RNL001 Renal Artery Obstruction 31 0.029
524
MXD032 Mixed Germ Cell Tumor 31 0.029
525
P ACT028 Acute Closed-Angle Glaucoma 30 0.029
526
SNG003 Single Ventricular Heart 30 0.029
527
SPP004 Suppurative Cholangitis 30 0.029
528
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 30 0.029
529
RSP007 Respiratory Distress Syndrome, Infant 30 0.029
530
c TST046 Testicular Germ Cell Tumor 1 29 0.029
531
PST092 Posttransplant Acute Limbic Encephalitis 29 0.029
532
MXD025 Mixed Germ Cell Cancer 28 0.029
533
P CNT036 Central Nervous System Germ Cell Tumor 28 0.029
534
TST020 Testis Seminoma 28 0.029
535
EXT001 Extragonadal Seminoma 27 0.029
536
c BNG021 Benign Essential Hypertension 26 0.029
537
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.029
538
URT049 Urate Oxidase, Pseudogene 25 0.029
539
HDG004 Hodgkin's Granuloma 23 0.029
540
HDG006 Hodgkin's Paragranuloma 22 0.029
541
HML018 Homologous Wasting Disease 22 0.029
542
SLF016 Sulfonamide Allergy 20 0.029
543
LTH043 Lithium Transport 18 0.029
544
DPH028 Diaphragmatic Flutter 13 0.029
545
RRP024 Rare Photodermatosis 12 0.029
546
TXC006 Toxic Labyrinthitis 11 0.029
547
ADR055 Adrenocortical Unresponsiveness to Acth with Postreceptor Defect 10 0.029
Content
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