Search results for Metformin

1472 hits were found for Metformin

# Family MCID Name MIFTS Score
1
c TYP009 Type 2 Diabetes Mellitus 92 44.519
2
P DBT009 Diabetes Mellitus 67 37.638
3
P PLY011 Polycystic Ovary Syndrome 57 27.608
4
c BLD140 Blood Group, I System 47 20.814
5
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 19.726
6
HYP056 Hypoglycemia 65 18.161
7
P LCT001 Lactic Acidosis 50 18.043
8
GST033 Gestational Diabetes 61 14.832
9
HYP066 Hyperglycemia 60 14.590
10
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 13.151
11
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 13.107
12
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 13.107
13
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 13.107
14
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 13.107
15
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 13.107
16
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 13.107
17
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 13.107
18
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 13.107
19
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 13.107
20
HYP060 Hyperinsulinism 53 12.978
21
FTT001 Fatty Liver Disease 61 11.414
22
NNL005 Non-Alcoholic Fatty Liver Disease 63 10.919
23
LPD008 Lipid Metabolism Disorder 61 10.495
24
END057 Endometrial Cancer 71 10.464
25
HYP043 Hyperandrogenism 47 10.085
26
P PRS040 Prostate Cancer 95 9.985
27
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 9.789
28
P BRS047 Breast Cancer 97 9.701
29
P PNC035 Pancreatic Cancer 86 9.596
30
GLC003 Glucose Intolerance 53 9.439
31
P INF032 Infertility 60 9.248
32
P CLR023 Colorectal Cancer 100 8.695
33
P LVR013 Liver Disease 68 8.632
34
PLY105 Polycystic Ovary Syndrome 1 39 8.619
35
P LNG032 Lung Cancer 98 8.067
36
ANV001 Anovulation 46 7.967
37
NNL006 Non-Alcoholic Steatohepatitis 54 7.906
38
c CHR684 Chronic Kidney Disease 74 7.884
39
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 7.881
40
AGN016 Aging 54 7.789
41
ANT039 Antisynthetase Syndrome 55 7.711
42
P OVR042 Ovarian Cancer 88 7.655
43
c TYP008 Type 1 Diabetes Mellitus 77 7.646
44
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 7.565
45
P TRN020 Turner Syndrome 67 7.527
46
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 7.520
47
P HPT023 Hepatocellular Carcinoma 95 7.423
48
P KDN018 Kidney Disease 72 7.406
49
P ANR048 Aniridia 1 66 7.166
50
c SML038 Small Cell Cancer of the Lung 69 7.128
51
ISC004 Ischemia 61 7.127
52
CNG034 Congestive Heart Failure 69 6.986
53
SQM006 Squamous Cell Carcinoma 59 6.966
54
48X005 48,xyyy 39 6.950
55
P ADN016 Adenocarcinoma 63 6.792
56
P HRT032 Heart Disease 84 6.739
57
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 6.698
58
RHB024 Rhabdomyosarcoma 2 65 6.668
59
PRD004 Prediabetes Syndrome 52 6.667
60
c PRC016 Pre-Eclampsia 64 6.632
61
VTM002 Vitamin B12 Deficiency 48 6.618
62
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 6.559
63
P CRN300 Coronary Heart Disease 1 73 6.469
64
c ACT071 Acute Kidney Failure 60 6.184
65
ART140 Arteries, Anomalies of 52 6.050
66
LPP008 Lipoprotein Quantitative Trait Locus 65 5.967
67
MTB004 Metabolic Acidosis 48 5.714
68
c MCR113 Microvascular Complications of Diabetes 3 52 5.697
69
GLB002 Glioblastoma 67 5.687
70
c ACT027 Acute Pancreatitis 60 5.631
71
ATH013 Atherosclerosis Susceptibility 63 5.577
72
P NRP001 Neuropathy 59 5.571
73
P DRR001 Diarrhea 55 5.559
74
c MCR133 Microvascular Complications of Diabetes 4 41 5.556
75
c MCR130 Microvascular Complications of Diabetes 6 41 5.556
76
c MCR120 Microvascular Complications of Diabetes 7 47 5.556
77
P PRD008 Periodontitis 64 5.545
78
P PNC044 Pancreatitis 61 5.518
79
END062 Endometrial Hyperplasia 48 5.516
80
P VSC007 Vascular Disease 62 5.514
81
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 5.498
82
P BLD134 Bladder Cancer 79 5.458
83
P HYP086 Hypothyroidism 69 5.453
84
P SCH015 Schizophrenia 74 5.453
85
P MYC007 Myocardial Infarction 69 5.268
86
PLC008 Placenta Disease 49 5.034
87
ADN018 Adenoma 58 4.990
88
P HPT021 Hepatitis 68 4.938
89
P MLN008 Melanoma 75 4.923
90
P ACN011 Acne 55 4.898
91
P PRP019 Peripheral Nervous System Disease 57 4.878
92
P ALC033 Alcohol Use Disorder 67 4.814
93
P ECL001 Eclampsia 52 4.810
94
PNC041 Pancreatic Ductal Adenocarcinoma 51 4.810
95
P HYP750 Hypertriglyceridemia, Familial 62 4.804
96
HYP266 Hypoxia 56 4.788
97
PRS047 Prostatitis 58 4.662
98
ADL002 Adult Syndrome 69 4.633
99
P LKM002 Leukemia 66 4.563
100
RNL114 Renal Cell Carcinoma, Nonpapillary 79 4.447
101
P DMN002 Dementia 65 4.441
102
THY029 Thyroid Carcinoma 54 4.422
103
ACN002 Acanthosis Nigricans 56 4.386
104
P BCL017 B-Cell Lymphoma 57 4.385
105
PNC129 Pancreatic Adenocarcinoma 65 4.380
106
c MCR115 Microvascular Complications of Diabetes 5 65 4.355
107
P LYM118 Lymphoma 69 4.354
108
P KDN017 Kidney Cancer 60 4.303
109
DWN001 Down Syndrome 70 4.301
110
DFC004 Deficiency Anemia 74 4.229
111
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 4.218
112
P ART022 Arthritis 70 4.217
113
c PRD040 Periodontitis, Chronic 52 4.172
114
OVR029 Ovarian Hyperstimulation Syndrome 63 4.172
115
GLM045 Glioma 62 4.170
116
GLL048 Glial Tumor 52 4.170
117
CRV035 Cervical Cancer 72 4.141
118
CVD001 Covid-19 58 4.139
119
OVR094 Ovarian Epithelial Cancer 39 4.136
120
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.129
121
PRP027 Peripheral Vascular Disease 71 4.093
122
P ALZ034 Alzheimer Disease 87 4.047
123
c HPT003 Hepatitis a 63 4.033
124
ART016 Aortic Aneurysm 69 4.026
125
c HPT001 Hepatitis C 61 4.020
126
ESP021 Esophageal Cancer 84 4.020
127
c HYP595 Hypertension, Essential 84 4.004
128
P GST053 Gastric Cancer 82 3.975
129
CLR108 Colorectal Adenoma 63 3.975
130
c ACT068 Acute Cystitis 61 3.945
131
ANR040 Aneurysm 60 3.932
132
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 3.927
133
LVR012 Liver Cirrhosis 62 3.915
134
MYL069 Myeloma, Multiple 77 3.903
135
P URN019 Urinary Tract Infection 49 3.884
136
CHL065 Cholangiocarcinoma 58 3.821
137
INT079 Intrahepatic Cholangiocarcinoma 51 3.821
138
P LNG064 Lung Cancer Susceptibility 3 70 3.805
139
P PLY014 Polycystic Kidney Disease 71 3.794
140
LPT014 Leptin Deficiency or Dysfunction 77 3.789
141
P LKM062 Leukemia, Acute Lymphoblastic 69 3.762
142
P RCT021 Rectum Cancer 54 3.731
143
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 3.717
144
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.693
145
NTR005 Nutritional Deficiency Disease 60 3.637
146
DPR016 Depression 65 3.629
147
ALC007 Alcohol Dependence 65 3.627
148
P PLM037 Pulmonary Hypertension 69 3.602
149
P ENC018 Encephalopathy 62 3.580
150
P MYC084 Mycobacterium Tuberculosis 1 68 3.560
151
AND005 Androgen Insensitivity Syndrome, Mild 21 3.559
152
SVR001 Severe Acute Respiratory Syndrome 68 3.559
153
EPT021 Epithelial Recurrent Erosion Dystrophy 46 3.540
154
STR067 Stroke, Ischemic 79 3.531
155
P THY032 Thyroiditis 56 3.524
156
PST011 Pustulosis of Palm and Sole 52 3.492
157
47X002 47,xyy 48 3.465
158
P ATR011 Atrial Fibrillation 66 3.457
159
P MSC005 Muscular Dystrophy 66 3.451
160
MLD018 Mild Cognitive Impairment 48 3.423
161
c HYP836 Hypercholesterolemia, Familial, 1 73 3.418
162
c PRS130 Prostate Cancer, Hereditary, 8 32 3.415
163
c PRS136 Prostate Cancer, Hereditary, 6 33 3.415
164
P RHM011 Rheumatoid Arthritis 81 3.413
165
AMN001 Amenorrhea 53 3.403
166
P PSR002 Psoriasis 63 3.395
167
c ACT075 Acute Myocardial Infarction 55 3.383
168
OST159 Osteogenic Sarcoma 66 3.378
169
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.358
170
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 3.349
171
TLN003 Telangiectasis 51 3.338
172
END086 End Stage Renal Disease 54 3.322
173
END041 Endometrial Adenocarcinoma 63 3.310
174
ORL011 Oral Cancer 60 3.308
175
P FRG001 Fragile X Syndrome 70 3.302
176
ALL029 Allergic Disease 61 3.295
177
c MJR024 Major Affective Disorder 9 40 3.290
178
c MJR022 Major Affective Disorder 8 37 3.290
179
P BPL003 Bipolar Disorder 56 3.290
180
DBT084 Diabetes Mellitus, Ketosis-Prone 60 3.289
181
RCK004 Rickets 65 3.282
182
P ATX030 Ataxia-Telangiectasia 80 3.262
183
IMM167 Immune Deficiency Disease 77 3.257
184
NRN004 Neuroendocrine Tumor 55 3.244
185
OST012 Osteoarthritis 77 3.244
187
MSC157 Muscular Dystrophy, Duchenne Type 79 3.201
188
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.188
189
THR024 Thrombosis 56 3.182
190
c ATS007 Autism Spectrum Disorder 72 3.166
191
DBT010 Diabetic Neuropathy 54 3.140
192
P HNT016 Huntington Disease 73 3.138
193
SKN019 Skin Melanoma 70 3.127
194
RPD005 Rapidly Involuting Congenital Hemangioma 48 3.121
195
P INS002 in Situ Carcinoma 53 3.120
196
c HYP724 Hyperlipoproteinemia, Type Iii 66 3.070
197
MNT002 Mental Depression 56 3.059
198
P CRD246 Cardiovascular System Disease 55 3.057
199
c TYP028 Type 1 Diabetes Mellitus 2 49 3.044
200
P OVR049 Ovarian Disease 50 3.029
201
c LKM061 Leukemia, Acute Myeloid 83 3.024
203
DFF005 Diffuse Large B-Cell Lymphoma 55 3.002
204
CHL068 Cholestasis 61 2.988
205
GLC008 Glucose Metabolism Disease 40 2.980
206
LNG099 Lung Disease 62 2.969
207
SCH012 Schizoaffective Disorder 49 2.961
208
CRB039 Cerebrovascular Disease 65 2.929
209
SQM013 Squamous Cell Carcinoma, Head and Neck 75 2.917
210
P SLP006 Sleep Apnea 69 2.902
211
P CHR345 Chronic Pain 50 2.878
212
PRT251 Proteinuria, Chronic Benign 58 2.855
213
LNG031 Lung Benign Neoplasm 51 2.841
214
LRY018 Laryngeal Squamous Cell Carcinoma 47 2.827
215
P FNG006 Feingold Syndrome 1 61 2.827
216
P MYL006 Myeloid Leukemia 60 2.803
217
CLT003 Colitis 63 2.794
218
HGH043 High Grade Glioma 46 2.779
219
END072 Endotheliitis 36 2.775
220
HYP080 Hypogonadism 49 2.766
221
THY030 Thyroid Gland Disease 50 2.743
222
P INF037 Inflammatory Bowel Disease 53 2.725
223
P LPS004 Lupus Erythematosus 61 2.724
224
BRN028 Brain Cancer 73 2.718
225
KRT002 Keratomalacia 54 2.709
226
ULC004 Ulcerative Colitis 74 2.700
227
ANX010 Anxiety 70 2.687
228
c PLM164 Pulmonary Hypertension, Primary, 1 80 2.686
229
P ATS364 Autism 72 2.685
230
P MCR129 Microvascular Complications of Diabetes 1 68 2.683
231
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.681
232
P CRD119 Cardiac Arrest 68 2.678
233
c HPT073 Hepatitis C Virus 71 2.650
234
FML035 Familial Hyperlipidemia 55 2.629
235
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.613
236
ORL015 Oral Squamous Cell Carcinoma 43 2.597
237
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 2.583
238
P MLT020 Multiple Sclerosis 79 2.578
239
P NRB001 Neuroblastoma 66 2.562
240
HDR003 Hidradenitis 50 2.560
241
HDR002 Hidradenitis Suppurativa 54 2.560
242
P GLM040 Glioma Susceptibility 1 70 2.538
243
SYS003 Systolic Heart Failure 49 2.532
244
PRT036 Peritonitis 65 2.498
245
P ART021 Arteriosclerosis 53 2.492
246
P TBR001 Tuberous Sclerosis 69 2.482
247
IMP005 Impotence 52 2.455
248
BRR014 Barrett Esophagus 66 2.448
249
CYT002 Cytokine Deficiency 43 2.447
250
CRB004 Cerebral Artery Occlusion 46 2.441
251
P PLM036 Pulmonary Fibrosis 65 2.427
252
MSC007 Muscle Hypertrophy 64 2.424
253
P MLN007 Male Infertility 56 2.408
254
AMD002 Amed Syndrome, Digenic 37 2.402
255
PRP080 Peripheral Artery Disease 54 2.378
256
HMN044 Human Immunodeficiency Virus Type 1 76 2.376
257
c TBR025 Tuberous Sclerosis 1 84 2.368
258
P MSC003 Muscular Atrophy 52 2.360
259
OCL069 Ocular Motor Apraxia 57 2.342
260
P LKM071 Leukemia, Chronic Lymphocytic 74 2.341
261
P SLP005 Sleep Disorder 62 2.338
262
c ATR087 Atrial Standstill 1 74 2.330
263
RNL077 Renal Fibrosis 46 2.322
264
ATM095 Autoimmune Disease 61 2.322
265
c SYS001 Systemic Lupus Erythematosus 86 2.318
266
BNR002 Bone Resorption Disease 47 2.313
267
P AST005 Asthma 76 2.311
268
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.305
269
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.301
270
ANG054 Angina Pectoris 65 2.289
271
PSY004 Psychotic Disorder 66 2.288
272
INT007 Intermediate Coronary Syndrome 53 2.278
273
c DRR009 Diarrhea 6 46 2.270
274
SVR004 Severe Combined Immunodeficiency 71 2.265
275
P MJR007 Major Affective Disorder 1 42 2.257
276
P RTN024 Retinoblastoma 72 2.233
277
ISL001 Islet Cell Tumor 55 2.232
278
CRH001 Crohn's Disease 80 2.229
279
LYM019 Lymphosarcoma 46 2.219
280
P MJR001 Major Depressive Disorder 68 2.212
281
SRC014 Sarcoma 64 2.212
282
SPN035 Spindle Cell Sarcoma 51 2.212
283
HPT004 Hepatic Coma 43 2.201
284
HPT019 Hepatic Encephalopathy 59 2.201
285
BRN071 Brain Injury 50 2.188
286
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.179
287
P DBT005 Diabetes Insipidus 54 2.176
288
MDD011 Mood Disorder 62 2.170
289
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.164
290
ACT088 Acute Insulin Response 39 2.162
291
P PTT006 Pituitary Adenoma 55 2.153
292
INS024 Insulin-Like Growth Factor I 77 2.135
293
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 2.122
294
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 37 2.119
295
BCK006 Back Pain 43 2.112
296
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.104
297
ATX019 Ataxia with Vitamin E Deficiency 44 2.104
298
P RSP003 Respiratory Failure 74 2.085
299
NRL016 Neural Tube Defects 81 2.071
300
P THR014 Thrombocytopenia 66 2.049
301
c PCH010 Pachyonychia Congenita 3 43 2.036
302
c GLL024 Gallbladder Disease 1 53 2.029
303
CLR109 Colorectal Adenocarcinoma 50 2.025
304
HYP020 Hyperprolactinemia 63 2.006
305
P SNS001 Sensorineural Hearing Loss 59 1.986
306
P SCK005 Sickle Cell Disease 56 1.986
307
P EXN002 Exanthem 58 1.985
308
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.982
309
c FNC027 Fanconi Anemia, Complementation Group a 81 1.957
310
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.952
311
P RTN016 Retinal Degeneration 52 1.941
312
c LKM063 Leukemia, Chronic Myeloid 71 1.930
313
c HPT016 Hepatitis B 62 1.930
314
HMC014 Homocysteinemia 52 1.924
315
P VSC018 Visceral Steatosis 32 1.914
316
P UVT001 Uveitis 57 1.907
317
SPN186 Spinal Cord Injury 61 1.902
318
P LFR001 Li-Fraumeni Syndrome 73 1.895
319
P PRS038 Personality Disorder 65 1.891
320
FBR047 Fibromyalgia 58 1.882
321
CNN003 Conn's Syndrome 77 1.880
322
SCH036 Scheie Syndrome 73 1.878
323
CRT016 Carotid Artery Disease 52 1.868
324
EWN003 Ewing Sarcoma 70 1.856
325
URT010 Ureteral Obstruction 45 1.855
326
P FBR017 Fibrosarcoma 55 1.855
327
PRS021 Prostatic Adenoma 43 1.854
328
MSC152 Muscular Dystrophy, Becker Type 69 1.851
329
c LFR007 Li-Fraumeni Syndrome 2 44 1.841
330
APP009 Appendix Adenocarcinoma 47 1.832
331
GNR004 Generalized Anxiety Disorder 55 1.828
332
VSC002 Vascular Dementia 59 1.827
333
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.816
334
P ADL010 Adult Respiratory Distress Syndrome 71 1.815
335
MCS002 Mucositis 55 1.809
336
ACR007 Acromegaly 70 1.809
337
c MCR112 Microvascular Complications of Diabetes 2 42 1.800
338
P FML011 Familial Adenomatous Polyposis 71 1.800
339
CRN036 Craniopharyngioma 63 1.794
340
P SKN015 Skin Carcinoma 71 1.784
341
P THL005 Thalassemia 56 1.776
342
P MTC069 Mitochondrial Disorders 57 1.776
343
PRS045 Prostatic Hypertrophy 52 1.770
344
CNS004 Constipation 56 1.765
345
PRS129 Prostatic Hyperplasia, Benign 48 1.763
346
ANR004 Anuria 44 1.763
347
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.759
348
P CYS039 Cystic Kidney Disease 52 1.749
349
MGL001 Megaloblastic Anemia 59 1.742
350
P PRK039 Parkinsonism 55 1.740
351
P FLL037 Follicular Lymphoma 73 1.737
352
P OST002 Osteoporosis 77 1.722
353
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.722
354
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.722
355
SKN016 Skin Disease 62 1.722
356
P HYP076 Hyperthyroidism 53 1.722
357
P END044 Endometriosis 62 1.716
358
P NSP012 Nasopharyngeal Carcinoma 60 1.716
359
P RTN018 Retinal Disease 53 1.715
360
P KHL003 Kohlschutter-Tonz Syndrome 57 1.702
361
CYS014 Cystadenocarcinoma 51 1.702
362
SRS001 Serous Cystadenocarcinoma 51 1.702
363
P CHN012 Chondrosarcoma 56 1.699
364
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.699
365
ATN004 Autonomic Neuropathy 42 1.692
366
P HML002 Hemolytic Anemia 62 1.688
367
P NTR004 Neutropenia 62 1.688
368
P OPN001 Open-Angle Glaucoma 55 1.686
369
c SPN225 Spondyloarthropathy 1 70 1.686
370
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.672
371
P LTR001 Lateral Sclerosis 58 1.672
372
SPL018 Splenomegaly 47 1.672
373
CRY036 Cryptogenic Cirrhosis 36 1.672
374
LYM040 Lymphoblastic Lymphoma 53 1.669
375
P HYP730 Hypogonadotropic Hypogonadism 54 1.668
376
HYP784 Hypogonadism, Male 43 1.668
377
P BND020 Bone Disease 60 1.668
378
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.660
379
P PRC019 Precocious Puberty 49 1.657
380
BNS007 Bone Sarcoma 51 1.641
381
ACT250 Acute Megakaryocytic Leukemia 63 1.641
382
HYP014 Hyperuricemia 51 1.635
383
P MYC008 Myocarditis 59 1.635
384
FTL021 Fetal Macrosomia 40 1.635
385
TXC005 Toxic Shock Syndrome 62 1.629
386
MYL009 Myelodysplastic Syndrome 67 1.624
387
BRS099 Breast Ductal Carcinoma 61 1.624
388
MMM006 Mammographic Density 39 1.624
389
c VRL010 Viral Hepatitis 52 1.622
390
GTR002 Goiter 52 1.622
391
BRN004 Brain Edema 54 1.621
392
c MJR008 Major Affective Disorder 2 34 1.621
393
c MJR006 Major Affective Disorder 5 32 1.621
394
c MJR003 Major Affective Disorder 6 32 1.621
395
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.621
396
c MJR004 Major Affective Disorder 4 28 1.621
397
c MJR023 Major Affective Disorder 7 33 1.621
398
P OCY003 Oocyte Maturation Defect 1 46 1.619
399
SPL004 Splenic Marginal Zone Lymphoma 50 1.606
400
c MGR028 Migraine with or Without Aura 1 64 1.606
401
APN008 Apnea, Obstructive Sleep 66 1.606
402
SFT003 Soft Tissue Sarcoma 57 1.606
403
P ANP001 Anaplastic Large Cell Lymphoma 61 1.586
404
c BTT014 Beta-Thalassemia 72 1.586
405
BTT017 Beta-Thalassemia Major 53 1.586
406
CYS009 Cystadenoma 43 1.586
407
CRC021 Carcinosarcoma 62 1.586
408
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 1.577
409
ACQ007 Acquired Immunodeficiency Syndrome 58 1.577
410
P MYT002 Myotonic Dystrophy 51 1.572
411
P DMN001 Diamond-Blackfan Anemia 73 1.565
412
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.565
413
HYP835 Hypothalamic Obesity 38 1.565
414
P BRB001 Beriberi 44 1.541
415
P SPP010 Suppressor of Tumorigenicity 3 51 1.541
416
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 1.530
417
P HMN038 Human Coronavirus Sensitivity 30 1.530
418
LPT006 Leptin Receptor Deficiency 50 1.530
419
SCH003 Schizophreniform Disorder 54 1.522
420
P INT099 Intrahepatic Cholestasis of Pregnancy 61 1.511
421
SPS057 Spasticity 43 1.511
422
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.506
423
THR012 Thoracic Cancer 44 1.473
424
NSP002 Nasopharyngitis 45 1.471
425
STT001 Status Epilepticus 58 1.469
426
TRM010 Traumatic Brain Injury 50 1.454
427
c FML001 Familial Atrial Fibrillation 65 1.447
428
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.447
429
PLS009 Plasma Cell Neoplasm 64 1.447
430
P CRV039 Cervicitis 52 1.447
431
RTC005 Reticulosarcoma 47 1.447
432
DSS032 Disease by Infectious Agent 55 1.446
433
INS001 Insulinoma 59 1.446
434
DSS008 Disease of Mental Health 74 1.435
435
PPL001 Papillary Adenoma 44 1.422
436
ART002 Arts Syndrome 66 1.422
437
P EPL164 Epilepsy 70 1.421
438
P BNG032 Benign Mesothelioma 53 1.421
439
P BRS044 Breast Adenocarcinoma 58 1.412
440
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 1.402
441
MNC019 Monocarboxylate Transporter 1 Deficiency 46 1.400
442
GT001 Gout 63 1.395
443
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.395
444
P GLL018 Gallbladder Cancer 53 1.386
445
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.384
446
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 1.384
447
P HDC001 Headache 56 1.384
448
c HYP272 Hypercholesterolemia, Familial, 3 46 1.375
449
DMP001 Dumping Syndrome 43 1.372
450
HLC007 Helicobacter Pylori Infection 67 1.368
451
P VSC011 Vasculitis 61 1.368
452
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.365
453
P SZR006 Seizure Disorder 69 1.358
454
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.348
455
FLL027 Fallopian Tube Carcinoma 66 1.348
456
PRT035 Peritoneum Cancer 45 1.348
457
HYP555 Hypertriglyceridemia, Transient Infantile 38 1.339
458
END040 Endogenous Depression 54 1.339
459
VRL011 Viral Infectious Disease 60 1.339
460
NRT001 Neurotic Disorder 56 1.339
461
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 1.332
462
PLM010 Pulmonary Edema 54 1.324
463
ECH003 Echinococcosis 52 1.323
464
RST023 Resting Heart Rate, Variation in 40 1.318
465
P PRV006 Pervasive Developmental Disorder 52 1.316
466
LMY014 Leiomyoma, Uterine 55 1.316
467
LMY002 Leiomyoma 51 1.316
468
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.300
469
P TRC086 Trichohepatoenteric Syndrome 1 60 1.281
470
CHL079 Children's Interstitial Lung Disease 26 1.281
471
LYM133 Lymphoma, Hodgkin, Classic 74 1.280
472
ACT119 Acute Promyelocytic Leukemia 62 1.280
473
BLR013 Biliary Tract Cancer 43 1.280
474
LMB062 Limb Ischemia 55 1.278
475
P ALP008 Alopecia 53 1.271
476
MLG169 Malignant Astrocytoma 57 1.265
477
BLR008 Bilirubin Metabolic Disorder 57 1.262
478
LTN029 Latent Autoimmune Diabetes in Adults 38 1.262
479
c BSL007 Basal Cell Carcinoma 68 1.261
480
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.261
481
BRN056 Bronchopulmonary Dysplasia 57 1.256
482
P INF038 Influenza 68 1.247
483
HYP005 Hypokalemia 55 1.244
484
FCT007 Factor Vii Deficiency 64 1.240
485
c PNS012 Paine Syndrome 60 1.240
486
P ATS366 Autism X-Linked 2 41 1.240
487
c PSR032 Psoriasis 11 47 1.240
488
CHP002 Chops Syndrome 47 1.240
489
c LKM056 Leukemia, Chronic Lymphocytic 2 47 1.240
490
P NJM001 Nijmegen Breakage Syndrome 75 1.240
491
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 1.240
492
c PSR023 Psoriasis 1 52 1.240
493
P PRC031 Preeclampsia/eclampsia 1 43 1.240
494
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.240
495
c PSR018 Psoriasis 13 40 1.240
496
c PSR028 Psoriasis 7 43 1.240
497
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 61 1.240
498
PNC015 Pancreatic Acinar Cell Adenocarcinoma 39 1.240
499
THY122 Thyroid Gland Cancer 59 1.240
500
ACN001 Acinar Cell Carcinoma 44 1.240
501
INT002 Intermittent Claudication 61 1.240
502
c PSR017 Psoriasis 2 53 1.240
503
TMR016 Tumor Suppressor Gene on Chromosome 11 28 1.240
504
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 57 1.240
505
EPT010 Epithelial-Myoepithelial Carcinoma 55 1.240
506
c BRS049 Breast Carcinoma in Situ 50 1.240
507
CLR003 Clear Cell Adenocarcinoma 50 1.240
508
ACN026 Acinar Cell Carcinoma of Pancreas 27 1.240
509
GST023 Gastric Ulcer 52 1.239
510
c ACT134 Acute Liver Failure 57 1.239
511
NNT012 Neonatal Jaundice 53 1.231
512
PSR001 Psoriatic Arthritis 61 1.231
513
ATY005 Atypical Teratoid Rhabdoid Tumor 69 1.220
514
ACT011 Acute Contagious Conjunctivitis 42 1.219
515
P CNJ013 Conjunctivitis 66 1.219
516
CYS001 Cystic Fibrosis 77 1.214
517
c OVR114 Ovarian Cancer 1 60 1.211
518
P ACQ022 Acquired Generalized Lipodystrophy 45 1.207
519
CRD137 Cardiogenic Shock 56 1.206
520
GRM004 Germinoma 40 1.204
521
GST045 Gastroenteritis 58 1.200
522
END021 Endomyocardial Fibrosis 56 1.198
523
c MYT029 Myotonia Congenita, Autosomal Recessive 42 1.198
524
SNS003 Sensory Peripheral Neuropathy 51 1.197
525
GST040 Gastric Adenocarcinoma 66 1.197
526
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 1.191
527
LMY003 Leiomyomatosis 43 1.191
528
INT020 Intravenous Leiomyomatosis 36 1.191
529
FHT001 Fh Tumor Predisposition Syndrome 26 1.191
530
MTY003 Mutyh Polyposis 38 1.191
531
PTT037 Pituitary Tumors 44 1.188
532
DMY004 Demyelinating Disease 50 1.188
533
c TYP058 Type 2 Diabetes 5 25 1.179
534
BCT022 Bacterial Infectious Disease 56 1.179
535
HYP082 Hypopharynx Cancer 47 1.179
536
P MYP004 Myopathy 67 1.179
537
P MVM001 Movement Disease 61 1.176
538
P EYD002 Eye Disease 57 1.176
539
MTC005 Mitochondrial Metabolism Disease 45 1.176
540
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 1.176
541
FML037 Female Breast Cancer 51 1.170
542
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.160
543
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.152
544
P MTR004 Maturity-Onset Diabetes of the Young 66 1.140
545
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.132
546
LYM143 Lymphoma, Non-Hodgkin, Familial 79 1.132
547
HSH003 Hashimoto Thyroiditis 60 1.132
548
P TMP001 Temporal Lobe Epilepsy 49 1.132
549
PMP014 Pemphigoid 49 1.124
550
BLL006 Bullous Pemphigoid 61 1.124
551
GRM005 Germ Cell Cancer 46 1.112
552
P OVR010 Ovarian Brenner Tumor 39 1.112
553
KLD004 Keloid Disorder 39 1.111
554
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.101
555
PLM001 Pulmonary Tuberculosis 69 1.101
556
ALL014 Allergic Encephalomyelitis 34 1.101
557
APH002 Aphasia 55 1.101
558
TRD006 Tardive Dyskinesia 53 1.101
559
P MTR014 Motor Neuron Disease 65 1.101
560
MLN073 Melanosis, Neurocutaneous 45 1.099
561
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.099
562
c FML346 Familial Adenomatous Polyposis 1 65 1.099
563
HYP081 Hypolipoproteinemia 49 1.099
564
CYT018 Cytochrome P450 2d6 Variant 26 1.099
565
MXD026 Mixed Glioma 45 1.099
566
CHR176 Chromophil Renal Cell Carcinoma 23 1.099
567
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.099
568
c PRM038 Primary Agammaglobulinemia 47 1.099
569
ART004 Aortic Atherosclerosis 46 1.090
570
c HNT011 Huntington Disease-Like 3 33 1.090
571
INT066 Interstitial Lung Disease 60 1.090
572
TRN015 Transient Cerebral Ischemia 62 1.074
573
c DWL002 Dowling-Degos Disease 1 58 1.067
574
CLN015 Colon Adenocarcinoma 64 1.067
575
P MYC033 Myoclonus 46 1.067
576
P FNC004 Fanconi Syndrome 60 1.063
577
c FML347 Familial Adenomatous Polyposis 2 56 1.063
578
JCB001 Jacobsen Syndrome 50 1.063
579
P ESP024 Esophagitis 60 1.063
580
PRM236 Primary Biliary Cholangitis 62 1.063
581
FND002 Fundus Dystrophy 55 1.063
582
PRM126 Primary Peritoneal Carcinoma 61 1.063
583
P OVR082 Overgrowth Syndrome 42 1.058
584
ADN027 Adenomyosis 59 1.055
585
PRX085 Preaxial Hallucal Polydactyly 28 1.055
586
ADR016 Adrenal Cortical Carcinoma 61 1.055
587
CLN044 Colon Adenoma 44 1.055
588
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.055
589
P PLY019 Polyneuropathy 53 1.055
590
ADR004 Adrenal Cortical Adenocarcinoma 38 1.055
591
ADR040 Adrenal Gland Pheochromocytoma 45 1.031
592
P PHC003 Pheochromocytoma 70 1.031
593
P GST044 Gastritis 55 1.031
594
IRR002 Irritable Bowel Syndrome 65 1.031
595
NDL007 Nodular Goiter 48 1.029
596
DYS073 Dysphagia 53 1.029
597
PRT013 Portal Hypertension 59 1.021
598
c CHR711 Chronic Asthma 41 1.021
599
HLL004 Hellp Syndrome 53 1.015
600
URL001 Urolithiasis 45 1.002
601
OVR063 Overnutrition 42 0.991
602
P PRK057 Parkinson Disease, Late-Onset 79 0.990
603
HYP025 Hyperphosphatemia 47 0.990
604
SBC016 Subacute Delirium 42 0.990
605
TST044 Testicular Torsion 45 0.986
606
ANR007 Anorexia Nervosa 59 0.986
607
RTN020 Retinal Vascular Disease 45 0.981
608
ANX004 Anoxia 40 0.981
609
CYS008 Cystic Echinococcosis 57 0.979
610
DBT002 Diabetic Autonomic Neuropathy 40 0.973
611
ERY051 Erythroleukemia, Familial 37 0.970
612
OHD004 Ohdo Syndrome 48 0.970
613
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 37 0.970
614
PLY161 Polymicrogyria, Bilateral Perisylvian, X-Linked 42 0.970
615
c INF071 Inflammatory Bowel Disease 1 65 0.970
616
ACR008 Acrocallosal Syndrome 70 0.970
617
ACR041 Acromelic Frontonasal Dysostosis 53 0.970
618
FRN006 Frontotemporal Dementia 68 0.970
619
c ATM099 Autoimmune Uveitis 44 0.970
620
ALK024 Alkuraya-Kucinskas Syndrome 45 0.970
621
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.970
622
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 0.970
623
P DST002 Distal Arthrogryposis 63 0.970
624
SPR126 Superior Semicircular Canal Dehiscence 41 0.970
625
P MDL005 Medulloblastoma 75 0.970
626
c ART144 Arthrogryposis, Distal, Type 1a 60 0.970
627
P BLR024 Biliary Cirrhosis, Primary, 1 28 0.970
628
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.970
629
HYP781 Hypoascorbemia 52 0.970
630
PPL049 Papillon-Lefevre Syndrome 65 0.970
631
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.970
632
CYS036 Cystinosis, Nephropathic 51 0.970
633
c SYS043 Systemic Lupus Erythematosus 1 38 0.970
634
SCK003 Sickle Cell Anemia 74 0.970
636
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.970
637
ACR006 Aceruloplasminemia 63 0.970
638
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.970
639
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 0.970
640
PCK003 Pick Disease of Brain 69 0.970
641
FLL041 Follicular Lymphoma 1 44 0.970
642
P ATX024 Ataxia-Oculomotor Apraxia 3 46 0.970
643
c PNT034 Pontocerebellar Hypoplasia, Type 2e 52 0.970
644
c PNT049 Pontocerebellar Hypoplasia, Type 2d 43 0.970
645
GLS018 Glass Syndrome 60 0.970
646
IMM064 Immunodeficiency, Common Variable, 10 43 0.970
647
VTM033 Vitamin K Deficiency Bleeding 50 0.970
648
c GLC092 Glaucoma, Primary Open Angle 61 0.970
649
CRC014 Carcinoid Tumors, Intestinal 46 0.970
650
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 0.970
651
PRC038 Precocious Puberty, Male-Limited 61 0.970
652
c LKM070 Leukemia, Acute Monocytic 56 0.970
653
CLC006 Calcinosis 47 0.970
654
HMG005 Hemoglobinopathy 55 0.970
655
ADN089 Adenosquamous Lung Carcinoma 49 0.970
656
ADN009 Adenosquamous Carcinoma 49 0.970
657
ADN012 Adenocarcinoma in Situ 42 0.970
658
TTH004 Tethered Spinal Cord Syndrome 41 0.970
659
SPS003 Spastic Diplegia 52 0.970
660
END035 Endocrine Gland Cancer 42 0.970
661
CRB037 Cerebral Palsy 67 0.970
662
HNT002 Hantavirus Pulmonary Syndrome 55 0.970
663
AZS001 Azoospermia 45 0.970
664
DNG003 Dengue Disease 65 0.970
665
GLS001 Gliosarcoma 63 0.970
666
ESP027 Esophagus Squamous Cell Carcinoma 45 0.970
667
CRB009 Cerebritis 43 0.970
668
MYF002 Myofascial Pain Syndrome 46 0.970
669
VGN023 Vaginitis 56 0.970
670
CLN045 Colonic Benign Neoplasm 48 0.970
672
c DYS119 Dystonia 9 54 0.970
673
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.970
674
c ALP101 Alpha-Thalassemia 62 0.970
675
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.970
676
NRM005 Neuromuscular Disease 63 0.970
677
MXD023 Mixed Cell Type Cancer 44 0.970
678
LKP003 Leukoplakia 39 0.970
680
IND017 Indolent Plasma Cell Myeloma 40 0.970
681
ORL006 Oral Mucosa Leukoplakia 22 0.970
682
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.970
683
P MLG074 Malignant Mesenchymoma 40 0.970
684
c CHR064 Chronic Monocytic Leukemia 36 0.970
685
TRP009 Triple X Syndrome 41 0.970
686
c HMG029 Hemoglobin Se Disease 41 0.970
687
P PRD037 Periodontal Ehlers-Danlos Syndrome 44 0.970
688
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.970
689
ERY023 Erythroplakia 22 0.970
690
ORL012 Oral Leukoplakia 35 0.970
691
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.970
692
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.970
693
CNG506 Congenital Amyoplasia 27 0.970
694
NPH009 Nephrolithiasis 54 0.970
695
c HNT004 Huntington Disease-Like 2 51 0.959
696
PPL022 Papilloma 53 0.959
697
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.948
698
LYM027 Lymphopenia 56 0.948
699
PRM329 Premature Aging 36 0.948
700
P RTN008 Retinitis Pigmentosa 79 0.936
701
MYC079 Myoclonic Epilepsy of Lafora 63 0.936
702
P PRG013 Paraganglioma 57 0.936
703
LWC001 Low Compliance Bladder 44 0.936
704
CHL067 Cholecystitis 59 0.936
705
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 0.936
706
DVR002 Diverticulitis 46 0.936
707
NRR001 Neuroretinitis 42 0.924
708
DBT081 Diabetic Encephalopathy 36 0.924
709
c MST023 Mesothelioma, Malignant 56 0.924
710
P THR015 Thrombophilia 51 0.924
711
RTN023 Retinitis 45 0.924
712
PRP030 Purpura 54 0.924
713
DGN001 Degenerative Disc Disease 48 0.924
714
NNC012 Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 17 0.924
715
GLC096 Galactorrhea 40 0.912
716
P SML001 Small Cell Carcinoma 52 0.912
717
c OPT053 Optic Atrophy 1 62 0.912
718
HRN029 Hearing Loss, Noise-Induced 37 0.912
719
ACT003 Acute Kidney Tubular Necrosis 46 0.912
720
CNT047 Contact Dermatitis 57 0.912
721
c DLT002 Dilated Cardiomyopathy 79 0.912
722
P GLM007 Glomerulonephritis 59 0.912
723
ALL010 Allergic Contact Dermatitis 56 0.912
724
P THY023 Thymoma 64 0.912
725
c THY107 Thymoma, Familial 42 0.912
726
RDC002 Radiculopathy 51 0.912
727
DRM006 Dermatitis 62 0.912
728
P GRF003 Graft-Versus-Host Disease 71 0.899
729
INT395 Intracranial Meningioma 48 0.899
730
P PRD006 Prader-Willi Syndrome 60 0.899
731
TST015 Testicular Disease 42 0.899
732
DNG002 Dengue Hemorrhagic Fever 59 0.899
733
P RHB003 Rhabdomyosarcoma 66 0.899
734
MNN043 Meningioma, Familial 79 0.899
735
CLR030 Clear Cell Renal Cell Carcinoma 54 0.899
736
SCR001 Secretory Meningioma 40 0.899
737
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.899
738
MYT011 Myotonia 38 0.899
739
HPT009 Hepatopulmonary Syndrome 48 0.899
740
ORP003 Oropharynx Cancer 54 0.899
741
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.899
742
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.888
743
ADR005 Adrenal Carcinoma 61 0.885
744
THY128 Thyroid Tumor 33 0.885
745
CRD132 Cardiac Conduction Defect 59 0.871
746
DYS015 Dysentery 50 0.871
747
P PYL005 Pyelonephritis 56 0.871
748
SDD008 Sudden Sensorineural Hearing Loss 41 0.871
749
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 0.870
750
P PNM007 Pneumonia 64 0.870
751
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.857
752
P END084 Endocrine System Disease 44 0.857
753
OST003 Osteonecrosis 61 0.856
754
URM002 Uremia 47 0.856
755
PRS063 Paresthesia 39 0.856
756
ERY003 Erythema Multiforme 56 0.840
757
CHD004 Chudley-Mccullough Syndrome 47 0.840
758
CYN002 Cyanosis, Transient Neonatal 43 0.840
759
GRW007 Growth Hormone Deficiency 47 0.840
760
FXD003 Fixed Drug Eruption 34 0.840
761
P RRT020 Rare Tumor 39 0.840
762
MNG006 Monogenic Diabetes 45 0.832
763
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 18 0.823
764
c SVR005 Severe Pre-Eclampsia 50 0.823
765
HYP026 Hypoglycemic Coma 37 0.823
766
MLG079 Malignant Pleural Mesothelioma 42 0.823
767
ETN001 Eating Disorder 59 0.811
768
P LCH002 Lichen Planus 55 0.805
769
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.805
770
HYP458 Hyper Ige Syndrome 60 0.801
771
RDN001 Reading Disorder 40 0.792
772
IRN002 Iron Metabolism Disease 56 0.789
773
P RNL007 Renal Tubular Acidosis 52 0.786
774
LNG039 Lung Squamous Cell Carcinoma 57 0.786
775
P URT039 Urticaria 57 0.786
776
P BRD002 Bardet-Biedl Syndrome 66 0.781
777
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.781
778
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.778
779
P SMP003 Simpson-Golabi-Behmel Syndrome 50 0.778
780
TRY001 Trypanosomiasis 50 0.767
781
c WLF013 Wolfram Syndrome 1 60 0.760
782
PPT005 Peptic Ulcer Disease 58 0.760
783
PTT057 Pituitary Adenoma 4, Acth-Secreting 48 0.758
784
PTT003 Pituitary-Dependent Cushing's Disease 39 0.758
785
P ACT010 Acth-Secreting Pituitary Adenoma 60 0.758
786
FNC007 Functioning Pituitary Adenoma 42 0.758
787
ACT055 Actinomycosis 55 0.758
788
P FML012 Familial Partial Lipodystrophy 54 0.754
789
OST017 Osteomyelitis 63 0.754
790
P HYP069 Hyperparathyroidism 62 0.754
791
ANG018 Angiomyolipoma 45 0.754
792
ACT162 Acute Sensory Ataxic Neuropathy 24 0.754
793
SBP001 Subependymal Giant Cell Astrocytoma 45 0.754
794
KDN015 Kidney Angiomyolipoma 46 0.754
795
ATS010 Autosomal Recessive Disease 42 0.742
796
P SHR029 Short Syndrome 58 0.742
797
P NNT058 Neonatal Diabetes 52 0.742
798
P TCD001 Tic Disorder 50 0.742
799
ADR007 Adrenoleukodystrophy 74 0.742
800
ADR022 Adrenomyeloneuropathy 39 0.742
801
GLM044 Glomerular Disease 34 0.742
802
HYP017 Hypophosphatemia 49 0.739
803
P CMP008 Compartment Syndrome 50 0.739
804
CRN322 Coronavirus Infectious Disease 37 0.729
805
P SLV026 Salivary Gland Carcinoma 60 0.729
806
P GRW001 Growth Hormone Secreting Pituitary Adenoma 47 0.729
807
P ALP004 Alport Syndrome 70 0.729
808
SQM002 Squamous Cell Papilloma 45 0.729
809
P MNC007 Monocytic Leukemia 48 0.729
810
NRM022 Neurometabolic Disease 23 0.729
811
P WLF004 Wolfram Syndrome 61 0.722
812
P GLL020 Gallbladder Disease 57 0.722
813
ANG020 Angiosarcoma 63 0.722
814
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.715
815
HYP114 Hypertensive Nephropathy 35 0.715
816
SPN051 Spondylitis 51 0.715
817
P ATR010 Atrial Heart Septal Defect 58 0.715
818
RCT020 Rectum Adenocarcinoma 48 0.715
819
HRT011 Heart Septal Defect 49 0.715
820
INF009 Inflammatory Spondylopathy 30 0.715
821
ATN005 Autonomic Dysfunction 45 0.715
822
DRG003 Drug Dependence 46 0.715
823
P ENC004 Encephalitis 61 0.715
824
DRG017 Drug-Induced Vasculitis 16 0.715
825
INT075 Intracranial Hypertension 52 0.710
826
MNT001 Mantle Cell Lymphoma 65 0.701
827
OTT002 Otitis Media 71 0.701
828
VLV047 Volvulus of Midgut 55 0.701
829
HPT067 Hepatocellular Adenoma 42 0.701
830
TRP003 Triple-Receptor Negative Breast Cancer 24 0.701
831
PLY023 Polycystic Liver Disease 62 0.701
832
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.701
833
ALS001 Alstrom Syndrome 65 0.701
834
P PRN023 Prion Disease 60 0.701
835
MCL006 Macular Retinal Edema 56 0.701
836
P BLD062 Bile Duct Cancer 68 0.701
837
P HYP077 Hypertrichosis 48 0.701
838
c ACT076 Acute Myocarditis 47 0.701
839
P TRT010 Teratoma 50 0.701
840
VLV010 Vulvovaginitis 42 0.701
841
P PLY018 Polycythemia 56 0.701
842
P MNN013 Meningitis 65 0.701
843
SYS071 Systemic Autoimmune Disease 35 0.701
844
P PHC019 Pheochromocytoma-Paraganglioma 35 0.701
845
P FNC044 Fanconi Anemia, Complementation Group C 56 0.686
846
P MYS003 Myasthenia Gravis 68 0.686
847
MCR013 Microphthalmia 60 0.686
848
INT067 Interstitial Nephritis 47 0.686
849
END080 Endometrial Disease 45 0.686
850
c ART115 Aortic Valve Disease 1 72 0.686
851
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.686
852
RCT035 Rectum Adenoma 20 0.686
853
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.686
854
EPS001 Epstein-Barr Virus Hepatitis 32 0.686
855
GRN004 Granulomatous Amebic Encephalitis 30 0.686
856
c FNC028 Fanconi Anemia, Complementation Group L 46 0.686
857
HRW001 Hair Whorl 35 0.686
858
KRT019 Keratitis, Hereditary 66 0.686
859
EXS001 Exostosis 49 0.686
860
ACS001 Acoustic Neuroma 56 0.686
861
CMP010 Complex Regional Pain Syndrome 59 0.686
862
ADR008 Adrenal Adenoma 55 0.686
863
HMS001 Hemosiderosis 48 0.686
864
GST037 Gastroparesis 52 0.686
865
GLL017 Gallbladder Adenocarcinoma 42 0.686
866
NRL005 Neurilemmoma 60 0.686
868
P CTR002 Cataract 59 0.686
869
PTH003 Pathologic Nystagmus 52 0.686
870
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.686
871
CRD016 Cardiac Rupture 34 0.686
872
HPT022 Hepatoblastoma 54 0.686
873
DBT006 Diabetic Macular Edema 48 0.686
874
CRT015 Carotid Artery Occlusion 45 0.686
875
ACN019 Acanthamoeba Keratitis 30 0.686
876
P RRH023 Rare Hereditary Hemochromatosis 53 0.686
877
PNM013 Pneumococcal Meningitis 43 0.686
878
TND005 Tendinitis 54 0.672
879
P DYS154 Dystonia 64 0.672
880
GST092 Gastroesophageal Reflux 60 0.670
881
PRG014 Progesterone Resistance 42 0.670
882
PLY001 Polycythemia Vera 69 0.670
883
c ANM038 Anemia, Autoimmune Hemolytic 63 0.670
884
PLY150 Polykaryocytosis Inducer 29 0.670
885
CLB022 Coloboma, Ocular, Autosomal Recessive 29 0.670
886
DCT002 Ductal Carcinoma in Situ 58 0.670
887
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.670
888
ALV002 Alveolar Echinococcosis 56 0.670
889
c FML021 Familial Hypercholesterolemia 71 0.670
890
RNL011 Renal Osteodystrophy 48 0.670
891
P INT068 Intestinal Disease 53 0.670
892
HYP006 Hypertensive Heart Disease 48 0.670
893
MCR141 Mucormycosis 59 0.670
894
RSC001 Rosacea 55 0.670
895
c PRG011 Progressive Myoclonus Epilepsy 40 0.670
896
c BCT013 Bacterial Pneumonia 47 0.670
897
P MYC026 Myoclonus Epilepsy 35 0.670
898
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.670
899
ARG004 Argyria 26 0.670
900
VSC053 Visceral Steatosis, Congenital 35 0.660
901
P ORF001 Orofaciodigital Syndrome 50 0.660
902
49X006 49, Xxxxy Syndrome 40 0.660
903
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.654
904
SPT003 Septic Myocarditis 23 0.654
905
RTN017 Retinal Detachment 60 0.654
906
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.654
907
SVR097 Severe Cutaneous Adverse Reaction 68 0.654
908
MLR004 Malaria 78 0.654
909
INT030 Intracranial Aneurysm 55 0.654
910
PRC003 Proctitis 49 0.654
911
BLN010 Balanitis 37 0.654
912
ACT017 Acute Chest Syndrome 50 0.654
913
P RTT002 Rett Syndrome 79 0.654
914
CRN030 Coronary Stenosis 50 0.654
915
SVR002 Severe Nonproliferative Diabetic Retinopathy 36 0.654
916
LNG030 Lung Adenoma 37 0.654
917
PLM039 Pulmonary Neuroendocrine Tumor 30 0.654
918
AMR003 Amaurosis Fugax 33 0.654
919
P AVS003 Avascular Necrosis 41 0.654
920
ERY066 Erythema Multiforme Major 29 0.654
921
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.654
922
c BRD010 Bardet-Biedl Syndrome 1 64 0.651
923
P PRG092 Pregnancy Loss, Recurrent 1 42 0.651
924
LRN001 Laurence-Moon Syndrome 45 0.651
925
c BRD014 Bardet-Biedl Syndrome 2 53 0.651
926
c BRD012 Bardet-Biedl Syndrome 11 51 0.651
927
c BRD013 Bardet-Biedl Syndrome 12 44 0.651
928
c BRD011 Bardet-Biedl Syndrome 10 49 0.651
929
ALN001 Aland Island Eye Disease 55 0.651
930
PPL007 Papillary Serous Adenocarcinoma 42 0.651
931
c PRS134 Prostate Cancer, Hereditary, 3 20 0.635
932
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.635
933
FTL006 Fetal Alcohol Spectrum Disorder 43 0.635
934
MRG003 Marginal Zone B-Cell Lymphoma 52 0.635
935
CMB007 Combined Immunodeficiency 56 0.635
936
ASP007 Aspiration Pneumonia 49 0.635
937
DNG001 Dengue Shock Syndrome 40 0.635
938
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.635
939
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.635
940
PRN011 Pernicious Anemia 52 0.635
941
HND015 Hand Skill, Relative 29 0.635
942
MNN017 Mononeuropathy 41 0.635
943
URN010 Urinary Tract Obstruction 55 0.635
944
NVS001 Neovascular Glaucoma 52 0.635
945
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.635
946
c NPH055 Nephrotic Syndrome, Type 1 52 0.635
947
PNN001 Panniculitis 52 0.635
949
END085 Endometrial Serous Adenocarcinoma 43 0.635
950
BRT037 Brittle Diabetes 24 0.635