Search results for Spironolactone

889 hits were found for Spironolactone

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 12.537
2
CNG034 Congestive Heart Failure 69 12.353
3
P HRT032 Heart Disease 84 9.690
4
c CHR684 Chronic Kidney Disease 73 8.610
5
HYP005 Hypokalemia 55 8.609
6
P ACN011 Acne 55 8.163
7
P KDN018 Kidney Disease 71 7.922
8
P PLY011 Polycystic Ovary Syndrome 57 7.850
9
c MCR133 Microvascular Complications of Diabetes 4 41 7.306
10
c MCR130 Microvascular Complications of Diabetes 6 41 7.306
11
c MCR120 Microvascular Complications of Diabetes 7 47 7.306
12
c MCR113 Microvascular Complications of Diabetes 3 52 7.159
13
PRT251 Proteinuria, Chronic Benign 58 6.412
14
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 6.310
15
c ATR087 Atrial Standstill 1 74 5.964
16
HYP043 Hyperandrogenism 47 5.756
17
END086 End Stage Renal Disease 54 5.687
18
INF021 Infant Gynecomastia 30 5.400
19
GYN001 Gynecomastia 48 5.400
20
P ATR011 Atrial Fibrillation 66 5.253
21
LVR012 Liver Cirrhosis 62 5.224
22
c TYP009 Type 2 Diabetes Mellitus 91 4.902
23
CNN003 Conn's Syndrome 77 4.675
24
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 4.555
25
P MYC007 Myocardial Infarction 69 4.295
26
P ALP008 Alopecia 53 4.134
27
PRT013 Portal Hypertension 59 4.116
28
SYS003 Systolic Heart Failure 49 4.064
29
c PLM164 Pulmonary Hypertension, Primary, 1 75 4.017
30
P DBT009 Diabetes Mellitus 67 3.951
31
c DLT002 Dilated Cardiomyopathy 79 3.797
32
c ACT071 Acute Kidney Failure 60 3.773
33
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 3.745
34
P LVR013 Liver Disease 68 3.712
35
DST006 Diastolic Heart Failure 45 3.428
36
P CRD119 Cardiac Arrest 68 3.426
37
P PLM037 Pulmonary Hypertension 69 3.417
38
CVD001 Covid-19 59 3.298
39
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.280
40
PRT036 Peritonitis 65 3.277
41
AND014 Androgenic Alopecia 46 3.270
42
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 3.232
43
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.232
44
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 3.232
45
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.232
46
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 3.232
47
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.232
48
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 3.232
49
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 3.232
50
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.232
51
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.232
52
FTT001 Fatty Liver Disease 61 3.231
53
P PRC019 Precocious Puberty 48 3.205
54
P HYP061 Hypertrophic Cardiomyopathy 68 3.174
55
P EXN002 Exanthem 58 3.156
56
SVR001 Severe Acute Respiratory Syndrome 68 3.126
57
c ACT075 Acute Myocardial Infarction 55 3.114
58
CNT060 Central Serous Chorioretinopathy 38 3.078
59
CRD132 Cardiac Conduction Defect 59 3.075
60
P CRD246 Cardiovascular System Disease 55 3.050
61
P ADL010 Adult Respiratory Distress Syndrome 70 3.006
62
BRN056 Bronchopulmonary Dysplasia 57 2.961
63
HDR002 Hidradenitis Suppurativa 54 2.919
64
HDR003 Hidradenitis 49 2.919
65
P GLM007 Glomerulonephritis 59 2.919
66
ALD013 Aldosterone-Producing Adenoma 36 2.902
67
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.900
68
PLY105 Polycystic Ovary Syndrome 1 39 2.881
69
P MSC005 Muscular Dystrophy 66 2.880
70
MSC157 Muscular Dystrophy, Duchenne Type 78 2.870
71
ALC007 Alcohol Dependence 65 2.858
72
ADR008 Adrenal Adenoma 55 2.842
73
P ALC033 Alcohol Use Disorder 67 2.842
74
LPD008 Lipid Metabolism Disorder 61 2.826
75
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.815
76
RNL077 Renal Fibrosis 46 2.791
77
P ALP061 Alopecia, Androgenetic, 1 48 2.787
78
P SLP006 Sleep Apnea 69 2.750
79
c MCR115 Microvascular Complications of Diabetes 5 65 2.749
80
P MCR129 Microvascular Complications of Diabetes 1 67 2.645
81
c MCR112 Microvascular Complications of Diabetes 2 42 2.645
82
c FML001 Familial Atrial Fibrillation 65 2.576
83
LNG099 Lung Disease 62 2.567
84
GLC003 Glucose Intolerance 53 2.531
85
ANT039 Antisynthetase Syndrome 55 2.505
86
P OVR049 Ovarian Disease 50 2.504
87
APP015 Apparent Mineralocorticoid Excess 57 2.481
88
ADN018 Adenoma 58 2.418
89
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.300
90
HYP006 Hypertensive Heart Disease 48 2.265
91
SNG003 Single Ventricular Heart 30 2.252
92
IMP005 Impotence 52 2.170
93
48X005 48,xyyy 39 2.166
94
PRC038 Precocious Puberty, Male-Limited 61 2.161
95
c BLD140 Blood Group, I System 47 2.134
96
RHB024 Rhabdomyosarcoma 2 65 2.072
97
MTB004 Metabolic Acidosis 48 2.064
98
c VRL005 Viral Pneumonia 52 2.062
99
SKN016 Skin Disease 63 2.062
100
MSC007 Muscle Hypertrophy 64 2.051
101
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.037
102
P TRN020 Turner Syndrome 67 2.037
103
P ACT105 Acute Mountain Sickness 52 2.036
104
ALC009 Alcoholic Liver Cirrhosis 54 2.019
105
PRM020 Premenstrual Tension 39 2.018
106
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 1.995
107
OST012 Osteoarthritis 77 1.995
108
MTR002 Mitral Valve Insufficiency 51 1.966
109
P ALP009 Alopecia Areata 59 1.939
110
HRT015 Heritable Pulmonary Arterial Hypertension 46 1.926
111
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 1.925
112
ADR041 Adrenal Cortical Adenoma 48 1.915
113
P MTR012 Mitral Valve Disease 57 1.902
114
VRC005 Varicose Veins 59 1.898
115
ATH013 Atherosclerosis Susceptibility 63 1.875
116
P NPH012 Nephrotic Syndrome 61 1.872
117
HYP025 Hyperphosphatemia 47 1.863
118
NNL006 Non-Alcoholic Steatohepatitis 54 1.853
119
GRN017 Granulocytopenia 42 1.843
120
P RNV001 Renovascular Hypertension 48 1.834
121
c HYP600 Hyperaldosteronism, Familial, Type Ii 30 1.832
123
P BRT004 Bartter Disease 58 1.798
124
P ANR048 Aniridia 1 66 1.788
125
HRN019 Hair-an Syndrome 19 1.787
126
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.776
127
END072 Endotheliitis 36 1.776
128
GLC008 Glucose Metabolism Disease 40 1.740
129
P ENC018 Encephalopathy 62 1.739
130
P PLY014 Polycystic Kidney Disease 71 1.689
131
IDP033 Idiopathic Edema 41 1.675
132
AGN016 Aging 53 1.659
133
HPT004 Hepatic Coma 43 1.649
134
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 1.645
135
APN008 Apnea, Obstructive Sleep 66 1.645
136
NWB001 Newborn Respiratory Distress Syndrome 56 1.645
137
AND005 Androgen Insensitivity Syndrome, Mild 21 1.645
138
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 35 1.645
139
LPP008 Lipoprotein Quantitative Trait Locus 65 1.643
140
HPT019 Hepatic Encephalopathy 59 1.595
141
HYP056 Hypoglycemia 65 1.590
142
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.580
143
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.580
144
P BRS047 Breast Cancer 97 1.576
145
AMN001 Amenorrhea 53 1.567
146
ISC004 Ischemia 61 1.566
147
ACN002 Acanthosis Nigricans 56 1.533
148
P DRR001 Diarrhea 55 1.521
149
P RNL007 Renal Tubular Acidosis 52 1.493
150
P SCH015 Schizophrenia 74 1.487
151
47X002 47,xyy 47 1.477
152
P PRS040 Prostate Cancer 95 1.470
153
P ALP004 Alport Syndrome 69 1.462
154
KHN001 Kuhnt-Junius Degeneration 48 1.462
155
NPH009 Nephrolithiasis 54 1.458
156
HYP066 Hyperglycemia 60 1.458
157
P HDC001 Headache 56 1.457
158
P MYC008 Myocarditis 59 1.450
159
ACR041 Acromelic Frontonasal Dysostosis 53 1.449
160
AMD002 Amed Syndrome, Digenic 36 1.449
161
c TYP008 Type 1 Diabetes Mellitus 77 1.449
162
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.449
163
ADL002 Adult Syndrome 69 1.449
164
HYP458 Hyper Ige Syndrome 60 1.449
165
c BNG021 Benign Essential Hypertension 37 1.448
166
P PNM007 Pneumonia 64 1.425
167
RTN017 Retinal Detachment 60 1.419
168
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 1.411
169
NPH010 Nephrosclerosis 50 1.390
170
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.382
171
LPT014 Leptin Deficiency or Dysfunction 77 1.382
172
CLC006 Calcinosis 47 1.382
173
CRH001 Crohn's Disease 80 1.382
174
P ART022 Arthritis 70 1.368
175
P SZR006 Seizure Disorder 69 1.367
176
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.321
177
GT001 Gout 63 1.321
178
P MYS003 Myasthenia Gravis 67 1.311
179
XRD010 Xeroderma Pigmentosum, Variant Type 72 1.296
180
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.278
181
OST062 Osteoarthritis with Mild Chondrodysplasia 46 1.278
182
P ALZ034 Alzheimer Disease 87 1.278
183
KND001 Kindler Syndrome 63 1.278
184
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 42 1.278
185
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 1.278
186
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.278
187
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.278
188
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 46 1.278
189
P HYP733 Hypercalciuria, Absorptive, 2 45 1.278
190
GLS018 Glass Syndrome 60 1.278
191
MLD018 Mild Cognitive Impairment 48 1.278
192
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 1.278
193
END021 Endomyocardial Fibrosis 56 1.278
194
KRT002 Keratomalacia 54 1.278
195
ALC010 Alcoholic Cardiomyopathy 42 1.278
196
DXT001 Dextrocardia 54 1.278
197
CHR078 Chorioretinitis 50 1.278
198
P VSC018 Visceral Steatosis 32 1.278
199
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.278
200
HYP706 Hypermobile Ehlers-Danlos Syndrome 54 1.278
201
RSP007 Respiratory Distress Syndrome, Infant 41 1.278
202
IDP073 Idiopathic Hypercalciuria 41 1.278
203
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.278
204
PLM184 Pulmonary Arterial Hypertension Associated with Congenital Heart Disease 42 1.278
205
c MGR028 Migraine with or Without Aura 1 63 1.262
206
CNT047 Contact Dermatitis 56 1.245
207
ART140 Arteries, Anomalies of 52 1.231
208
PLM010 Pulmonary Edema 54 1.228
209
CHL068 Cholestasis 61 1.225
210
P HYP098 Hypereosinophilic Syndrome 66 1.224
211
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.206
212
DRG024 Drug Allergy 40 1.192
213
PRT019 Protein-Losing Enteropathy 44 1.192
214
MLN073 Melanosis, Neurocutaneous 45 1.187
215
c MJR022 Major Affective Disorder 8 37 1.177
216
c MJR024 Major Affective Disorder 9 40 1.177
217
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 1.177
218
P BPL003 Bipolar Disorder 56 1.177
219
P URN019 Urinary Tract Infection 48 1.177
220
RSC001 Rosacea 55 1.174
221
P MRC003 Mercury Poisoning 48 1.174
222
FML037 Female Breast Cancer 51 1.172
223
URM002 Uremia 47 1.172
224
BRN004 Brain Edema 54 1.163
225
HYP020 Hyperprolactinemia 63 1.160
226
P HYP076 Hyperthyroidism 53 1.160
227
P NTR004 Neutropenia 62 1.157
228
ATM095 Autoimmune Disease 61 1.147
229
HYP060 Hyperinsulinism 53 1.147
230
PMP014 Pemphigoid 48 1.147
231
P DBT005 Diabetes Insipidus 54 1.147
232
P MMB011 Membranous Nephropathy 50 1.135
233
P ATS364 Autism 72 1.134
234
P MJR007 Major Affective Disorder 1 42 1.134
235
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.118
236
DPR016 Depression 64 1.118
237
P ATT013 Attention Deficit-Hyperactivity Disorder 65 1.110
238
P RHM011 Rheumatoid Arthritis 81 1.108
239
P HYP069 Hyperparathyroidism 62 1.105
240
P LNG028 Long Qt Syndrome 63 1.100
241
OCL069 Ocular Motor Apraxia 57 1.094
242
P URT039 Urticaria 57 1.094
243
P PRD021 Periodic Paralysis 42 1.094
244
MNT002 Mental Depression 56 1.081
245
P INF032 Infertility 60 1.079
246
c MLG069 Malignant Hypertension 46 1.064
247
CRB039 Cerebrovascular Disease 65 1.061
248
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 1.061
249
P HMP007 Hemophilia 52 1.049
250
P PLM036 Pulmonary Fibrosis 65 1.048
251
P VSC007 Vascular Disease 62 1.039
252
ERY003 Erythema Multiforme 56 1.031
253
GLB002 Glioblastoma 67 1.031
254
GLM044 Glomerular Disease 34 1.031
255
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.027
256
NPH003 Nephrocalcinosis 49 1.018
257
STR067 Stroke, Ischemic 79 1.014
258
ALL029 Allergic Disease 61 1.013
259
P HYP120 Hypoaldosteronism 33 1.007
260
CRD223 Cardiac Arrhythmia 63 0.994
261
c LNG047 Long Qt Syndrome 2 59 0.986
262
CRN019 Coronary Artery Vasospasm 47 0.986
263
CLT003 Colitis 63 0.985
264
HPT014 Hepatorenal Syndrome 49 0.985
265
P MYP004 Myopathy 67 0.985
266
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.977
267
c LKM061 Leukemia, Acute Myeloid 83 0.977
268
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.977
269
P LKM002 Leukemia 65 0.977
270
P END084 Endocrine System Disease 44 0.977
271
P MYL006 Myeloid Leukemia 60 0.977
272
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.977
273
P GST044 Gastritis 55 0.973
274
QDR001 Quadriplegia 49 0.973
275
P RNL015 Renal Hypertension 45 0.973
276
PRS045 Prostatic Hypertrophy 53 0.973
277
BLM002 Bulimia Nervosa 56 0.951
278
c XRD032 Xeroderma Pigmentosum, Complementation Group B 50 0.951
279
c SCN007 Secondary Hyperparathyroidism 50 0.937
280
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.924
281
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.911
282
P LYM118 Lymphoma 66 0.910
283
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.910
284
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.910
285
GLC106 Glucocorticoid Resistance, Generalized 47 0.910
287
ANT078 Antipyrine Metabolism 24 0.899
288
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.897
289
SXL003 Sexual Disorder 49 0.897
290
ESP002 Esophageal Varix 51 0.897
291
P PRD008 Periodontitis 63 0.897
292
P FNG006 Feingold Syndrome 1 61 0.885
293
SYN036 Syncope 44 0.883
294
TRM010 Traumatic Brain Injury 50 0.883
295
BRN071 Brain Injury 50 0.883
296
ALL010 Allergic Contact Dermatitis 55 0.880
297
BNR002 Bone Resorption Disease 47 0.868
298
CRB004 Cerebral Artery Occlusion 45 0.868
299
VRC001 Varicocele 48 0.868
300
BLL006 Bullous Pemphigoid 61 0.868
301
HYP540 Hypertension, Diastolic 38 0.866
302
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.853
303
THR024 Thrombosis 56 0.853
304
c ATM022 Autoimmune Myocarditis 35 0.853
305
SCH014 Schistosomiasis 56 0.853
306
P SYS005 Systemic Scleroderma 73 0.823
307
CNG064 Congenital Chloride Diarrhea 34 0.820
308
P SNS001 Sensorineural Hearing Loss 60 0.820
309
CRN027 Corneal Neovascularization 47 0.820
310
CYT002 Cytokine Deficiency 43 0.820
311
P FML187 Familial Hypertension 34 0.820
312
SDD008 Sudden Sensorineural Hearing Loss 41 0.820
313
c LNG044 Long Qt Syndrome 1 66 0.806
314
DWN001 Down Syndrome 70 0.806
315
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.806
316
P HMN038 Human Coronavirus Sensitivity 30 0.806
317
HMT008 Hematuria, Benign Familial 54 0.806
318
IMM167 Immune Deficiency Disease 76 0.806
319
SDD001 Sudden Infant Death Syndrome 60 0.806
320
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.806
321
HMR039 Hemorrhage, Intracerebral 57 0.806
322
CMR002 Coumarin Resistance 59 0.806
323
HMN044 Human Immunodeficiency Virus Type 1 76 0.806
324
END040 Endogenous Depression 54 0.806
325
P HMR003 Hemorrhagic Disease 59 0.806
326
NRT001 Neurotic Disorder 56 0.806
327
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.806
328
P RTN018 Retinal Disease 53 0.806
329
ACQ007 Acquired Immunodeficiency Syndrome 58 0.806
330
c CHR064 Chronic Monocytic Leukemia 35 0.806
331
LYM019 Lymphosarcoma 46 0.806
332
c CRD027 Cardiomyopathy Due to Anthracyclines 9 0.806
333
URT010 Ureteral Obstruction 44 0.802
334
FBR047 Fibromyalgia 57 0.802
335
c JVN010 Juvenile Rheumatoid Arthritis 52 0.802
336
SPL018 Splenomegaly 47 0.802
337
P INF037 Inflammatory Bowel Disease 53 0.783
338
P ANG015 Angioedema 56 0.783
339
P SKN015 Skin Carcinoma 71 0.783
340
P THR014 Thrombocytopenia 66 0.783
341
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.783
342
P THY032 Thyroiditis 56 0.783
343
CRY036 Cryptogenic Cirrhosis 36 0.783
344
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.763
345
c NPH049 Nephrotic Syndrome, Type 2 49 0.763
346
PHR003 Pharyngitis 57 0.763
347
KDN001 Kidney Cortex Necrosis 31 0.763
348
PPL022 Papilloma 53 0.763
349
SQM002 Squamous Cell Papilloma 45 0.763
350
MDD011 Mood Disorder 61 0.763
351
P ART018 Aortic Valve Insufficiency 52 0.763
352
ETN001 Eating Disorder 59 0.763
353
c ATS007 Autism Spectrum Disorder 71 0.741
354
SCR003 Secretory Diarrhea 35 0.741
355
c DWL002 Dowling-Degos Disease 1 58 0.741
356
HSH003 Hashimoto Thyroiditis 60 0.741
357
P RSP003 Respiratory Failure 73 0.741
358
DRG002 Drug-Induced Hepatitis 42 0.741
359
URN010 Urinary Tract Obstruction 55 0.741
360
CHL014 Cholera 62 0.741
361
P OVR046 Ovarian Cyst 43 0.741
362
HYP266 Hypoxia 56 0.741
363
P CRN300 Coronary Heart Disease 1 73 0.722
364
c SPN225 Spondyloarthropathy 1 70 0.716
365
P BLD134 Bladder Cancer 79 0.716
366
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.716
367
P HYP750 Hypertriglyceridemia, Familial 61 0.716
368
P TTR001 Tetralogy of Fallot 69 0.716
369
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.716
370
CHR008 Choroiditis 48 0.716
371
P DDN001 Duodenal Ulcer 52 0.716
372
P PYL005 Pyelonephritis 56 0.716
373
SPN051 Spondylitis 51 0.716
374
P OBS001 Obstructive Jaundice 49 0.716
375
P INN002 Inner Ear Disease 49 0.716
376
P HYP077 Hypertrichosis 48 0.716
377
TRN007 Transsexualism 38 0.716
378
INF009 Inflammatory Spondylopathy 30 0.716
379
MLT035 Multifocal Choroiditis 31 0.716
380
HDN002 Head Injury 44 0.716
381
TRG002 Trigeminal Neuralgia 61 0.688
382
HYP008 Hypertensive Retinopathy 39 0.688
383
P HYP730 Hypogonadotropic Hypogonadism 57 0.688
384
PSD009 Pseudohermaphroditism 46 0.688
385
MMB001 Membranoproliferative Glomerulonephritis 56 0.688
386
P END044 Endometriosis 62 0.688
387
ART016 Aortic Aneurysm 68 0.688
388
THR123 Thrombotic Microangiopathy 40 0.688
389
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.688
390
BCK005 Becker Nevus Syndrome 33 0.655
391
HLX001 Helix Syndrome 47 0.655
392
P HYP058 Hypervitaminosis a 47 0.655
393
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.655
394
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.655
395
TLM001 Telomere Length, Mean Leukocyte 17 0.655
396
GST023 Gastric Ulcer 52 0.655
397
PRP030 Purpura 54 0.655
398
BRS099 Breast Ductal Carcinoma 61 0.655
399
P PRP029 Porphyria 60 0.655
400
P HYP040 Hypospadias 51 0.655
401
RCK004 Rickets 64 0.655
402
P HML002 Hemolytic Anemia 62 0.655
403
c ACQ014 Acquired Hemophilia 45 0.655
404
PRT058 Pure Autonomic Failure 58 0.655
405
MYP060 Myopic Macular Degeneration 19 0.655
406
GNT163 Genetic Alopecia 4 0.655
407
LFT001 Left Bundle Branch Hemiblock 47 0.648
408
c HYP836 Hypercholesterolemia, Familial, 1 73 0.626
409
c WLM013 Wilms Tumor 1 65 0.612
410
P PNC035 Pancreatic Cancer 87 0.612
411
c ART101 Aortic Valve Disease 2 65 0.612
412
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.612
413
c HRD002 Hereditary Angioedema 61 0.612
414
P HML001 Hemolytic-Uremic Syndrome 52 0.612
415
FML036 Familial Periodic Paralysis 43 0.612
416
P RRT020 Rare Tumor 39 0.612
417
FML159 Familial Periodic Paralyses 16 0.612
418
GTL001 Gitelman Syndrome 65 0.606
419
P HPT021 Hepatitis 68 0.574
420
ADR005 Adrenal Carcinoma 58 0.574
421
CNT015 Central Sleep Apnea 46 0.574
422
ADR057 Adrenogenital Syndrome 31 0.541
423
P PRP003 Porphyria Cutanea Tarda 66 0.508
424
P END047 Endophthalmitis 53 0.508
425
ART074 Aortic Dissection 53 0.508
426
P LCH002 Lichen Planus 54 0.508
427
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.508
428
KWS002 Kawasaki Disease 65 0.498
429
P HPT023 Hepatocellular Carcinoma 95 0.498
430
BCT022 Bacterial Infectious Disease 55 0.498
431
P END033 Endocarditis 58 0.498
432
c ACT068 Acute Cystitis 60 0.498
433
P INF038 Influenza 68 0.498
434
P MNN013 Meningitis 65 0.498
435
P HRP006 Herpes Simplex 65 0.498
436
P PHC003 Pheochromocytoma 70 0.416
437
ADR040 Adrenal Gland Pheochromocytoma 45 0.416
438
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.394
439
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.394
440
APR006 Apert Syndrome 69 0.394
441
BHR001 Behr Syndrome 51 0.394
442
CPL013 Capillary Malformations, Congenital 53 0.394
443
FCT001 Factor Viii Deficiency 61 0.394
444
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.394
445
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.394
446
c MJR008 Major Affective Disorder 2 34 0.394
447
c PNS012 Paine Syndrome 60 0.394
448
c HYP272 Hypercholesterolemia, Familial, 3 46 0.394
449
c MJR006 Major Affective Disorder 5 32 0.394
450
c MJR023 Major Affective Disorder 7 33 0.394
451
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.394
452
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 0.394
453
c HMP029 Hemophilia a 69 0.394
454
HYP781 Hypoascorbemia 52 0.394
455
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.394
456
BRD001 Brody Myopathy 55 0.394
457
c MJR004 Major Affective Disorder 4 28 0.394
458
c MJR003 Major Affective Disorder 6 32 0.394
459
CYT005 Cytomegalovirus Retinitis 50 0.394
460
P HMN010 Hemangioma 61 0.394
461
RNL001 Renal Artery Obstruction 31 0.394
462
BLD051 Blood Coagulation Disease 52 0.394
463
NTR005 Nutritional Deficiency Disease 60 0.394
464
P EPL164 Epilepsy 70 0.394
465
NRR001 Neuroretinitis 42 0.394
466
P CPL006 Capillary Hemangioma 53 0.394
467
PPL001 Papillary Adenoma 44 0.394
468
VSL002 Visual Epilepsy 39 0.394
469
c HPT003 Hepatitis a 63 0.394
470
RTN023 Retinitis 45 0.394
471
MNN020 Meningococcal Infection 44 0.394
472
ATX019 Ataxia with Vitamin E Deficiency 44 0.394
473
c BCT007 Bacterial Meningitis 55 0.394
474
NSS002 Neisseria Meningitidis Infection 46 0.394
475
ANV001 Anovulation 46 0.375
476
INT007 Intermediate Coronary Syndrome 53 0.375
477
P LDD007 Liddle Syndrome 1 57 0.360
478
ATS010 Autosomal Recessive Disease 42 0.345
479
c THR092 Thrombophilia Due to Thrombin Defect 74 0.345
480
ATR057 Atrioventricular Block 54 0.329
481
c HYP731 Hyperaldosteronism, Familial, Type I 59 0.329
482
c PRC016 Pre-Eclampsia 64 0.329
483
P LPS004 Lupus Erythematosus 61 0.329
484
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.312
485
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.312
486
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.312
487
ADR016 Adrenal Cortical Carcinoma 61 0.294
488
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.294
489
P KDN017 Kidney Cancer 60 0.294
490
ADR004 Adrenal Cortical Adenocarcinoma 38 0.294
491
CRD137 Cardiogenic Shock 56 0.294
492
c PRM093 Premature Ovarian Failure 7 47 0.275
493
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.275
494
P MJR001 Major Depressive Disorder 68 0.275
495
TRC022 Tricuspid Valve Insufficiency 46 0.275
496
P PSD003 Pseudohypoaldosteronism 45 0.275
497
P PNC025 Panic Disorder 52 0.275
498
MCC012 Mccune-Albright Syndrome 69 0.255
499
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.255
500
PST028 Post-Traumatic Stress Disorder 58 0.255
501
SKN005 Skin Atrophy 41 0.255
502
HRT012 Heart Valve Disease 53 0.255
503
c PRM005 Primary Hyperparathyroidism 59 0.255
504
PRT037 Pertussis 49 0.255
505
ANR040 Aneurysm 60 0.255
506
DFC004 Deficiency Anemia 74 0.232
507
P SRC025 Sarcoidosis 1 70 0.232
508
ART002 Arts Syndrome 66 0.232
509
RST023 Resting Heart Rate, Variation in 40 0.232
510
c GRV008 Graves Disease 1 54 0.232
511
PRP080 Peripheral Artery Disease 54 0.232
512
HYP014 Hyperuricemia 51 0.232
513
P HYP086 Hypothyroidism 68 0.232
514
CHG001 Chagas Disease 65 0.232
515
EST004 Estrogen Excess 37 0.232
516
PRT029 Parathyroid Adenoma 51 0.232
517
ART010 Arteriolosclerosis 37 0.232
518
PLY012 Polyhydramnios 46 0.232
519
ATN005 Autonomic Dysfunction 45 0.232
520
INT075 Intracranial Hypertension 52 0.232
521
ANX010 Anxiety 70 0.208
522
ANG054 Angina Pectoris 65 0.208
523
HYP114 Hypertensive Nephropathy 35 0.208
524
BDD001 Budd-Chiari Syndrome 62 0.208
525
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.208
526
P CHN059 Chondrocalcinosis 51 0.208
527
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.208
528
PPL021 Papilledema 49 0.208
529
c HPT001 Hepatitis C 61 0.208
530
CNS004 Constipation 56 0.208
531
P PTT006 Pituitary Adenoma 55 0.208
532
P PRL003 Proliferative Glomerulonephritis 43 0.208
533
END062 Endometrial Hyperplasia 47 0.208
534
P LCT001 Lactic Acidosis 50 0.208
535
c FML191 Familial Long Qt Syndrome 54 0.208
536
SYS071 Systemic Autoimmune Disease 35 0.208
537
P FML156 Familial Hyperaldosteronism 39 0.208
538
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.180
539
CYS001 Cystic Fibrosis 77 0.180
540
c BRN108 Branchiootic Syndrome 1 63 0.180
541
BNB002 Bainbridge-Ropers Syndrome 45 0.180
542
c PCH010 Pachyonychia Congenita 3 43 0.180
543
P ORT004 Orthostatic Intolerance 61 0.180
544
P MGR003 Migraine with Aura 51 0.180
545
P ART021 Arteriosclerosis 53 0.180
546
HYP080 Hypogonadism 49 0.180
547
ACR007 Acromegaly 70 0.180
548
RTN020 Retinal Vascular Disease 45 0.180
549
NRN004 Neuroendocrine Tumor 55 0.180
550
P ECL001 Eclampsia 52 0.180
551
OVR063 Overnutrition 42 0.180
552
IRN002 Iron Metabolism Disease 56 0.180
553
c VRL010 Viral Hepatitis 52 0.180
554
P RHN004 Rhinitis 56 0.180
555
THY030 Thyroid Gland Disease 50 0.180
556
c ACT076 Acute Myocarditis 46 0.180
557
GTR002 Goiter 52 0.180
558
PRM236 Primary Biliary Cholangitis 62 0.180
559
P GRV001 Graves' Disease 54 0.180
560
RTN003 Retinal Ischemia 48 0.180
561
P GLL022 Guillain-Barre Syndrome 59 0.180
562
P FCL005 Focal Segmental Glomerulosclerosis 57 0.180
563
URL001 Urolithiasis 45 0.180
564
LKS001 Leukostasis 40 0.180
565
NRN001 Neuroendocrine Carcinoma 47 0.180
566
P CTR002 Cataract 59 0.180
567
P BCL017 B-Cell Lymphoma 57 0.180
568
P NRB001 Neuroblastoma 66 0.180
569
KDN013 Kidney Hypertrophy 33 0.180
570
P HYP055 Hypoplastic Left Heart Syndrome 65 0.180
571
BRK012 Broken Heart Syndrome 42 0.180
572
RNL034 Renal Cell Carcinoma 4 16 0.180
573
P THY054 Thyrotoxic Periodic Paralysis 51 0.180
574
IRR002 Irritable Bowel Syndrome 64 0.180
575
GRW007 Growth Hormone Deficiency 47 0.180
576
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.180
577
RRC029 Rare Cause of Hypertension 13 0.180
578
OGL001 Ogilvie Syndrome 24 0.180
579
DYS073 Dysphagia 53 0.180
580
P HYP265 Hypotonia 42 0.180
581
PLM186 Pulmonary Arterial Hypertension Associated with Portal Hypertension 25 0.180
582
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.147
583
MYL009 Myelodysplastic Syndrome 67 0.147
584
LNG108 Langerhans Cell Histiocytosis 57 0.147
585
P PTS002 Ptosis 52 0.147
586
DFF010 Diffuse Alopecia Areata 23 0.147
587
OSM001 Osmotic Diarrhea 27 0.147
588
c ART120 Arthrogryposis, Distal, Type 3 50 0.147
589
P NNN008 Noonan Syndrome 1 76 0.147
590
c SCL052 Scleroderma, Familial Progressive 60 0.147
591
GLC096 Galactorrhea 40 0.147
592
INS024 Insulin-Like Growth Factor I 77 0.147
593
SPP011 Suppression of Tumorigenicity 12 61 0.147
594
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.147
595
PRP027 Peripheral Vascular Disease 71 0.147
596
HYP017 Hypophosphatemia 49 0.147
597
P SML001 Small Cell Carcinoma 52 0.147
598
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.147
599
CYN002 Cyanosis, Transient Neonatal 43 0.147
600
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.147
601
ASC009 Ascites, Chylous 31 0.147
602
PRP009 Peripartum Cardiomyopathy 54 0.147
603
HYP748 Hypertelorism 46 0.147
604
HRW001 Hair Whorl 35 0.147
605
P BND020 Bone Disease 60 0.147
606
DFF005 Diffuse Large B-Cell Lymphoma 55 0.147
607
c HRD202 Hereditary Lymphedema I 54 0.147
608
TRY001 Trypanosomiasis 50 0.147
609
P VNS003 Venous Insufficiency 54 0.147
610
MGC001 Megacolon 48 0.147
611
THR004 Thrombocytosis 52 0.147
612
VCC001 Vaccinia 49 0.147
613
HST010 Histiocytosis 49 0.147
614
P ATR010 Atrial Heart Septal Defect 58 0.147
615
TLG001 Telogen Effluvium 31 0.147
616
P LMY004 Leiomyosarcoma 62 0.147
617
P BRS053 Breast Fibroadenoma 48 0.147
618
P MLN007 Male Infertility 56 0.147
619
HRT011 Heart Septal Defect 49 0.147
620
RHM028 Rheumatic Heart Disease 55 0.147
621
HMP001 Hemopericardium 47 0.147
622
MCL006 Macular Retinal Edema 56 0.147
623
P MYP006 Myopia 55 0.147
624
P MTR003 Mitral Valve Stenosis 53 0.147
625
HMP005 Hemiplegia 53 0.147
626
IGG001 Iga Glomerulonephritis 50 0.147
627
MRP001 Morphine Dependence 41 0.147
628
LYD001 Leydig Cell Tumor 45 0.147
629
PRS042 Prostate Disease 42 0.147
630
P PSD015 Pseudohypoparathyroidism 54 0.147
631
NRM005 Neuromuscular Disease 62 0.147
632
CLN006 Colonic Pseudo-Obstruction 31 0.147
633
P TRT010 Teratoma 50 0.147
634
TST014 Testicular Cancer 51 0.147
635
P PRC012 Pericardial Effusion 50 0.147
636
P HYD006 Hydrocephalus 62 0.147
637
P HYP024 Hypoparathyroidism 55 0.147
638
LMY002 Leiomyoma 51 0.147
639
SLP001 Sleeping Sickness 56 0.147
640
GND002 Gender Identity Disorder 40 0.147
641
TXC001 Toxic Megacolon 37 0.147
642
ADR001 Adrenal Rest Tumor 31 0.147
643
PRC013 Pericarditis 53 0.147
644
ACT084 Acute Stress Disorder 53 0.147
645
BRN024 Bronchitis 67 0.147
646
HYP034 Hypertensive Encephalopathy 43 0.147
647
ADR012 Adrenal Gland Disease 44 0.147
648
ULC004 Ulcerative Colitis 74 0.147
649
PPT005 Peptic Ulcer Disease 58 0.147
650
P MSC003 Muscular Atrophy 52 0.147
651
GLM045 Glioma 62 0.147
652
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.147
653
PTT037 Pituitary Tumors 44 0.147
654
c PSD047 Pseudo-Turner Syndrome 52 0.147
655
c SCN052 Secondary Adrenal Insufficiency 35 0.147
656
PRS063 Paresthesia 39 0.147
657
GLL048 Glial Tumor 51 0.147
658
IDP095 Idiopathic Steroid-Resistant Nephrotic Syndrome 20 0.147
659
THY029 Thyroid Carcinoma 55 0.147
660
INF034 Infective Endocarditis 53 0.104
661
P SCL018 Scoliosis 57 0.104
662
MLR004 Malaria 77 0.104
663
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.104
664
CRT065 Cortisone Reductase Deficiency 1 25 0.104
665
P APL001 Aplastic Anemia 72 0.104
666
APH002 Aphasia 55 0.104
667
UMB002 Umbilical Hernia 46 0.104
668
FRS012 First-Degree Atrioventricular Block 39 0.104
669
SCN049 Second-Degree Atrioventricular Block 34 0.104
670
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.104
671
PNG002 Pain Agnosia 51 0.104
672
P PRS062 Persistent Hyperplastic Primary Vitreous 48 0.104
673
ASP007 Aspiration Pneumonia 49 0.104
674
c ART115 Aortic Valve Disease 1 72 0.104
675
c VSC019 Vesicoureteral Reflux 1 56 0.104
676
c ANM038 Anemia, Autoimmune Hemolytic 63 0.104
677
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.104
678
c SYS001 Systemic Lupus Erythematosus 85 0.104
679
c MYT021 Myotonic Dystrophy 1 67 0.104
680
P OST002 Osteoporosis 76 0.104
681
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 61 0.104
682
c SML038 Small Cell Cancer of the Lung 68 0.104
683
P HYP534 Hypomagnesemia 3, Renal 46 0.104
684
BTT016 Batten-Turner Congenital Myopathy 54 0.104
685
c NPH055 Nephrotic Syndrome, Type 1 52 0.104
686
P CRC039 Coarctation of Aorta 46 0.104
687
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.104
688
P FML018 Familial Mediterranean Fever 73 0.104
689
GLC012 Galactosialidosis 55 0.104
690
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.104
691
c PSD108 Pseudohypoparathyroidism, Type Ia 64 0.104
692
GST092 Gastroesophageal Reflux 59 0.104
693
OST159 Osteogenic Sarcoma 66 0.104
694
AND002 Androgen Insensitivity Syndrome 63 0.104
695
c MLG151 Malignant Hyperthermia 5 29 0.104
696
HMC014 Homocysteinemia 52 0.104
697
c LNG048 Long Qt Syndrome 3 52 0.104
698
WLS001 Wilson Disease 70 0.104
699
DSS032 Disease by Infectious Agent 55 0.104
700
c HPT073 Hepatitis C Virus 70 0.104
701
c ACT004 Acute Diarrhea 40 0.104
702
FDB001 Foodborne Botulism 55 0.104
703
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 60 0.104
704
MSC152 Muscular Dystrophy, Becker Type 69 0.104
705
CYS013 Cystinuria 66 0.104
706
P CRP001 Carpal Tunnel Syndrome 65 0.104
707
LMY014 Leiomyoma, Uterine 55 0.104
708
HYP780 Hypoadrenocorticism, Familial 61 0.104
709
MYL005 Myelofibrosis 70 0.104
710
P HMN036 Hemangiopericytoma, Malignant 56 0.104
711
INT303 Intracranial Hypertension, Idiopathic 56 0.104
712
P LPR021 Leprosy 3 71 0.104
713
P SJG008 Sjogren Syndrome 60 0.104
714
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.104
715
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.104
716
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.104
717
P GRF003 Graft-Versus-Host Disease 71 0.104
719
c LKM063 Leukemia, Chronic Myeloid 70 0.104
720
SVR097 Severe Cutaneous Adverse Reaction 68 0.104
721
PHS019 Phosphohydroxylysinuria 17 0.104
722
MCR302 Macrostomia, Isolated 29 0.104
723
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.104
724
BRK010 Burkitt Lymphoma 65 0.104
726
MRF001 Marfan Syndrome 76 0.104
727
MNR012 Meniere Disease 55 0.104
728
P ALG028 Alagille Syndrome 1 73 0.104
729
c PSD090 Pseudohypoaldosteronism, Type Iia 31 0.104
730
NVS017 Nevus, Epidermal 66 0.104
731
END057 Endometrial Cancer 76 0.104
732
ASP030 Aspirin Resistance 41 0.104
733
OVR029 Ovarian Hyperstimulation Syndrome 63 0.104
734
P MLT008 Multinodular Goiter 41 0.104
735
P MYG005 Myoglobinuria 40 0.104
736
P LFT003 Left Ventricular Noncompaction 58 0.104
737
HMN047 Human Cytomegalovirus Infection 59 0.104
738
P TRN034 Transverse Myelitis 47 0.104
739
c CHR708 Chronic Urticaria 42 0.104
740
CRY014 Cryptococcal Meningitis 48 0.104
741
INT067 Interstitial Nephritis 46 0.104
742
P VNT002 Ventricular Septal Defect 58 0.104
743
P CYS018 Cystitis 58 0.104
744
P RCT021 Rectum Cancer 54 0.104
745
CLN015 Colon Adenocarcinoma 64 0.104
746
DNT012 Dental Caries 53 0.104
747
MYL031 Myeloproliferative Neoplasm 66 0.104
748
PPL002 Papillary Carcinoma 46 0.104
749
MYL001 Myelitis 49 0.104
750
P TMP001 Temporal Lobe Epilepsy 49 0.104
751
P TCD001 Tic Disorder 50 0.104
752
c BSL007 Basal Cell Carcinoma 67 0.104
753
PLM029 Palmoplantar Keratosis 48 0.104
754
P SCK002 Sick Sinus Syndrome 55 0.104
755
NRT004 Neuritis 53 0.104
756
P BNC003 Bone Cancer 58 0.104
757
c MLG084 Malignant Fibrous Histiocytoma 62 0.104
758
P OST001 Osteopetrosis 70 0.104
759
PNM008 Pneumothorax 54 0.104
760
P ICH004 Ichthyosis 56 0.104
761
CRT020 Cortisone Reductase Deficiency 36 0.104
762
CNS002 Constrictive Pericarditis 39 0.104
763
PRT011 Protein C Deficiency 47 0.104
764
CLR030 Clear Cell Renal Cell Carcinoma 53 0.104
765
P PRP019 Peripheral Nervous System Disease 57 0.104
766
FLL008 Folliculitis 45 0.104
767
ART008 Arteriosclerosis Obliterans 40 0.104
768
P NML001 Nemaline Myopathy 49 0.104
769
CNN005 Connective Tissue Disease 66 0.104
770
LPT001 Leptospirosis 65 0.104
771
P LTR001 Lateral Sclerosis 57 0.104
772
P INT143 Interstitial Cystitis 59 0.104
773
RNL008 Renal Artery Atheroma 24 0.104
774
IRN001 Iron Deficiency Anemia 58 0.104
775
LYM157 Lymph Node Carcinoma 33 0.104
776
GST037 Gastroparesis 52 0.104
777
P ESP024 Esophagitis 60 0.104
778
BRC012 Brucellosis 66 0.104
779
ANR004 Anuria 44 0.104
780
P ANT006 Antiphospholipid Syndrome 55 0.104
781
MYM001 Myoma 54 0.104
782
SYN007 Synovitis 54 0.104
783
PLM001 Pulmonary Tuberculosis 69 0.104
784
TRC021 Tricuspid Valve Stenosis 31 0.104
785
P SYP003 Syphilis 59 0.104
786
SPN035 Spindle Cell Sarcoma 51 0.104
787
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.104
788
CRN036 Craniopharyngioma 63 0.104
789
P RST002 Restrictive Cardiomyopathy 54 0.104
790
ORC001 Orchitis 43 0.104
791
OST004 Osteitis Fibrosa 38 0.104
792
BNN003 Bone Inflammation Disease 47 0.104
793
P BRS044 Breast Adenocarcinoma 58 0.104
794
CRN030 Coronary Stenosis 50 0.104
795
PLC002 Plica Syndrome 35 0.104
796
ATN004 Autonomic Neuropathy 42 0.104
797
PNL012 Penile Cancer 57 0.104
798
PRT018 Portal Vein Thrombosis 50 0.104
799
GST033 Gestational Diabetes 60 0.104
800
PRD004 Prediabetes Syndrome 52 0.104
801
MLD002 Mild Pre-Eclampsia 33 0.104
802
ENP001 Enophthalmos 40 0.104
803
MCR018 Microcytic Anemia 46 0.104
804
P ART005 Arteriovenous Malformation 64 0.104
805
END028 Endemic Goiter 36 0.104
806
P ERY036 Erythema Nodosum 49 0.104
807
NRG002 Neurogenic Bladder 54 0.104
808
P MTH008 Methylmalonic Acidemia 52 0.104
809
PNN001 Panniculitis 52 0.104
810
LYM022 Lymphangioma 54 0.104
811
AZS001 Azoospermia 45 0.104
812
OLG001 Oligospermia 45 0.104
813
ACT003 Acute Kidney Tubular Necrosis 46 0.104
814
PLS006 Plasmodium Vivax Malaria 51 0.104
815
SRC014 Sarcoma 64 0.104
816
P END046 Endometritis 46 0.104
817
CHL004 Cholelithiasis 48 0.104
818
P DRM010 Dermatomyositis 61 0.104
819
P OPT009 Optic Neuritis 57 0.104
820
DYS015 Dysentery 49 0.104
821
c SVR005 Severe Pre-Eclampsia 49 0.104
822
P MLN008 Melanoma 75 0.104
823
P SLP005 Sleep Disorder 61 0.104
824
CHR074 Choriocarcinoma 46 0.104
825
BRS051 Breast Disease 58 0.104
826
PRC001 Pericoronitis 28 0.104
827
DVR002 Diverticulitis 46 0.104
828
CHR048 Chronic Rhinitis 46 0.104
829
P FBR003 Fibrous Histiocytoma 43 0.104
830
P MYT002 Myotonic Dystrophy 51 0.104
832
ACQ011 Acquired Agranulocytosis 10 0.104
833
AQG004 Aquagenic Syringeal Acrokeratoderma 17 0.104
834
P HMC002 Homocystinuria 52 0.104
835
PLC007 Placental Abruption 47 0.104
836
DBT006 Diabetic Macular Edema 48 0.104
837
STT002 Status Asthmaticus 49 0.104
838
PLM033 Pulmonary Embolism 58 0.104
839
P MLG056 Malignant Hyperthermia 65 0.104
840
P HYP083 Hypopituitarism 51 0.104
841
TRT003 Tertiary Syphilis 36 0.104
842
CRT028 Cor Triatriatum 25 0.104
843
CRT061 Cor Triatriatum Dexter 20 0.104
844
HNS001 Hansen's Disease 32 0.104
845
MLT037 Multifocal Lymphangioendotheliomatosis with Thrombocytopenia 17 0.104
846
NWD001 New Daily-Persistent Headache 20 0.104
847
NDL013 Nodular Regenerative Hyperplasia 46 0.104
848
SBC016 Subacute Delirium 42 0.104
849
P NRP001 Neuropathy 59 0.104
850
P TXP001 Toxoplasmosis 59 0.104
851
P C1Q005 C1q Nephropathy 21 0.104
852
CHF001 Chief Cell Adenoma 22 0.104
853
GST050 Gastrointestinal System Disease 55 0.104
854
CMP035 Complete Atrioventricular Canal 24 0.104
855
P DST107 Distal Renal Tubular Acidosis 48 0.104
856
RMT001 Remitting Seronegative Symmetrical Synovitis with Pitting Edema 17 0.104
857
P AMY004 Amyloidosis 69 0.104
858
c BCT013 Bacterial Pneumonia 47 0.104
859
NRM001 Neuromyelitis Optica 60 0.104
860
CRC006 Carcinoid Syndrome 55 0.104
861
EXP004 Exophthalmos 50 0.104
862
P PLY017 Polyarteritis Nodosa 59 0.104
863
ANX004 Anoxia 40 0.104
864
DMD001 Demodicidosis 23 0.104
865
MSN011 Mesangioproliferative Glomerulopathy 11 0.104
866
DRG003 Drug Dependence 46 0.104
867
c ALM001 Al Amyloidosis 54 0.104
868
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.104
869
CNG491 Congenital Portosystemic Shunt 17 0.104
870
MTB016 Metabolic Myopathy 30 0.104
871
SFT003 Soft Tissue Sarcoma 43 0.104
872
TRC096 Trichothiodystrophy 56 0.104
873
CRR012 Cirrhotic Cardiomyopathy 22 0.104
874
NNS045 Non-Specific Syndromic Intellectual Disability 41 0.104
875
ACR120 Acrokeratoderma 13 0.104
876
MLG163 Malignant Tumor of Penis 29 0.104
877
ERY066 Erythema Multiforme Major 29 0.104
878
c TRN053 Transient Pseudohypoaldosteronism 24 0.104
879
HYP855 Hyperpigmentation of the Skin 25 0.104
880
HYP625 Hyperandrogenism Due to Cortisone Reductase Deficiency 15 0.104
881
P RRC004 Rare Cardiomyopathy 16 0.104
882
P PLM064 Pulmonary Sequestration 22 0.104
883
PRN039 Paraneoplastic Syndromes 37 0.104
884
SPN186 Spinal Cord Injury 60 0.104
885
P RRL003 Rare Lymphatic Malformation 31 0.104
886
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.104
887
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.104
888
P OVR082 Overgrowth Syndrome 41 0.104
889
ACT245 Acth-Dependent Cushing Syndrome 22 0.104
Content
Loading form....