Search results for Caffeine

1506 hits were found for Caffeine

# Family MCID Name MIFTS Score
1
APN006 Apnea of Prematurity 24 19.359
2
P HDC001 Headache 57 18.153
3
c MGR028 Migraine with or Without Aura 1 64 15.932
4
P MLG056 Malignant Hyperthermia 66 15.098
5
BRN056 Bronchopulmonary Dysplasia 56 13.301
6
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 10.004
7
P TRM003 Tremor 48 9.888
8
ANX010 Anxiety 70 9.632
9
HYP266 Hypoxia 57 9.537
10
WTH001 Withdrawal Disorder 48 9.377
11
TLN003 Telangiectasis 51 9.287
12
P ATX030 Ataxia-Telangiectasia 80 9.278
13
P PNC025 Panic Disorder 52 8.660
14
P SZR006 Seizure Disorder 70 8.456
15
P PRK057 Parkinson Disease, Late-Onset 80 8.453
16
P SLP005 Sleep Disorder 61 8.248
17
P ATT013 Attention Deficit-Hyperactivity Disorder 64 7.979
18
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 7.787
19
ALC007 Alcohol Dependence 66 7.763
20
PSY004 Psychotic Disorder 66 7.758
21
OST159 Osteogenic Sarcoma 66 7.724
22
PNG002 Pain Agnosia 51 7.619
23
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 7.251
24
P ATR011 Atrial Fibrillation 66 7.179
25
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 7.167
26
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 7.167
27
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 7.167
28
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 7.167
29
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 7.167
30
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 7.167
31
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 7.167
32
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 7.167
33
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 7.167
34
P PRK039 Parkinsonism 55 7.148
35
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 7.124
36
FTT001 Fatty Liver Disease 62 7.098
37
SBS004 Substance Dependence 47 7.064
38
P PTN014 Patent Ductus Arteriosus 1 59 6.934
39
P ALC033 Alcohol Use Disorder 61 6.897
40
P SKN015 Skin Carcinoma 71 6.888
41
NNL005 Non-Alcoholic Fatty Liver Disease 63 6.827
42
P SBS003 Substance Abuse 54 6.665
43
XRD010 Xeroderma Pigmentosum, Variant Type 73 6.618
44
TTN003 Tetanus 65 6.606
45
P CRN300 Coronary Heart Disease 1 73 6.498
46
MLG086 Malignant Hyperthermia Susceptibility 39 6.452
47
LVR012 Liver Cirrhosis 63 6.421
48
48X005 48,xyyy 39 6.291
49
LPP008 Lipoprotein Quantitative Trait Locus 65 6.268
50
AGN016 Aging 54 6.241
51
c TYP009 Type 2 Diabetes Mellitus 92 6.229
52
ISC004 Ischemia 61 6.210
53
P NRB001 Neuroblastoma 66 6.166
54
P SLP006 Sleep Apnea 69 6.159
55
ART140 Arteries, Anomalies of 53 6.132
56
HYP056 Hypoglycemia 65 6.113
57
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 5.936
58
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 5.890
59
BRS051 Breast Disease 58 5.834
60
c EXD008 Exudative Vitreoretinopathy 1 71 5.821
61
CRB037 Cerebral Palsy 67 5.782
62
P LVR013 Liver Disease 69 5.778
63
P OST002 Osteoporosis 76 5.754
64
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 5.754
65
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 5.754
66
P DMN002 Dementia 66 5.744
67
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 5.676
68
P OVR042 Ovarian Cancer 88 5.567
69
BRN071 Brain Injury 50 5.449
70
P CRD119 Cardiac Arrest 67 5.421
71
CCN002 Cocaine Abuse 49 5.350
72
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 5.332
73
P MYP004 Myopathy 67 5.310
74
HYP005 Hypokalemia 55 5.287
75
P HNT016 Huntington Disease 73 5.258
76
c HPT001 Hepatitis C 62 5.249
77
P ALZ034 Alzheimer Disease 87 5.209
78
ENT011 Enterocolitis 55 5.172
79
P SCH015 Schizophrenia 74 5.166
80
CLF027 Cleft Palate, Isolated 64 5.166
81
HYP066 Hyperglycemia 61 5.104
82
PRT037 Pertussis 65 5.076
83
CRD223 Cardiac Arrhythmia 63 5.051
84
INT323 Intraocular Pressure Quantitative Trait Locus 64 5.041
85
RPD005 Rapidly Involuting Congenital Hemangioma 46 5.027
86
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 5.024
87
PRN019 Perinatal Necrotizing Enterocolitis 60 4.982
88
47X002 47,xyy 48 4.908
89
P DBT009 Diabetes Mellitus 67 4.900
90
P INF032 Infertility 57 4.882
91
GLM045 Glioma 63 4.882
92
GLL048 Glial Tumor 52 4.864
93
RST023 Resting Heart Rate, Variation in 40 4.858
94
c HYP595 Hypertension, Essential 85 4.816
95
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.814
96
P LTR001 Lateral Sclerosis 58 4.814
97
P MJR001 Major Depressive Disorder 68 4.796
98
TRM010 Traumatic Brain Injury 51 4.794
99
MNT002 Mental Depression 57 4.729
100
P HRT032 Heart Disease 81 4.698
101
LWC001 Low Compliance Bladder 45 4.679
102
P ENC018 Encephalopathy 62 4.642
103
DRG003 Drug Dependence 46 4.622
104
BCK006 Back Pain 47 4.580
105
TBC004 Tobacco Addiction 63 4.545
106
c MLG147 Malignant Hyperthermia 1 45 4.514
107
P RSP003 Respiratory Failure 74 4.494
108
NNL006 Non-Alcoholic Steatohepatitis 54 4.473
109
GLB002 Glioblastoma 67 4.417
110
P CHR345 Chronic Pain 50 4.415
111
CYT002 Cytokine Deficiency 43 4.405
112
P CTR002 Cataract 60 4.373
113
P CLR023 Colorectal Cancer 100 4.280
114
P OPN001 Open-Angle Glaucoma 55 4.278
115
P ART022 Arthritis 71 4.272
116
ETN001 Eating Disorder 59 4.264
117
BRN002 Bronchiolitis 57 4.237
118
ATH013 Atherosclerosis Susceptibility 63 4.136
119
P ALP008 Alopecia 54 4.120
120
OCL006 Ocular Hypertension 53 4.111
121
P HPT021 Hepatitis 69 4.074
122
P MLN008 Melanoma 76 4.057
123
P MVM001 Movement Disease 61 4.038
124
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.038
125
SPN035 Spindle Cell Sarcoma 54 4.014
126
SRC014 Sarcoma 65 4.014
127
P RNV001 Renovascular Hypertension 49 4.004
128
P PSR002 Psoriasis 63 4.004
129
PST011 Pustulosis of Palm and Sole 52 4.004
130
END057 Endometrial Cancer 72 3.988
131
c GLC092 Glaucoma, Primary Open Angle 62 3.973
132
HRW001 Hair Whorl 35 3.967
133
AMD002 Amed Syndrome, Digenic 37 3.952
134
MDD011 Mood Disorder 62 3.935
135
c EPS039 Episodic Pain Syndrome, Familial, 1 42 3.931
136
ALL029 Allergic Disease 59 3.929
137
MTB004 Metabolic Acidosis 48 3.919
138
DPR016 Depression 65 3.903
139
DWN001 Down Syndrome 70 3.897
140
GT001 Gout 64 3.896
141
c PRC016 Pre-Eclampsia 65 3.894
142
P LNG032 Lung Cancer 98 3.876
143
CYT018 Cytochrome P450 2d6 Variant 26 3.871
144
c MJR022 Major Affective Disorder 8 38 3.861
145
c MJR024 Major Affective Disorder 9 41 3.861
146
P BPL003 Bipolar Disorder 56 3.861
147
PRM020 Premenstrual Tension 39 3.851
148
P SMK004 Smoking As a Quantitative Trait Locus 3 44 3.849
149
MLD018 Mild Cognitive Impairment 48 3.840
150
P NRC002 Narcolepsy 56 3.817
151
P KDN018 Kidney Disease 72 3.811
152
P BRS047 Breast Cancer 98 3.807
153
SPN186 Spinal Cord Injury 61 3.806
154
HLX001 Helix Syndrome 48 3.804
155
AND014 Androgenic Alopecia 47 3.796
156
OBS002 Obsessive-Compulsive Disorder 68 3.789
157
P RST001 Restless Legs Syndrome 52 3.777
158
AMN003 Amnestic Disorder 54 3.767
159
P MYC007 Myocardial Infarction 70 3.750
160
ANX004 Anoxia 40 3.748
161
SBC016 Subacute Delirium 43 3.742
162
P MGR001 Migraine Without Aura 49 3.740
163
HYP060 Hyperinsulinism 54 3.717
164
c ESS001 Essential Tremor 57 3.713
165
P BLD134 Bladder Cancer 79 3.711
166
P DRM053 Dermatitis, Atopic 65 3.704
167
BLM002 Bulimia Nervosa 57 3.702
168
ILS001 Ileus 50 3.681
169
P PLY014 Polycystic Kidney Disease 69 3.663
170
c PNS012 Paine Syndrome 60 3.660
171
GLC003 Glucose Intolerance 54 3.640
172
P MSC005 Muscular Dystrophy 67 3.632
173
LPT014 Leptin Deficiency or Dysfunction 78 3.607
174
GST092 Gastroesophageal Reflux 61 3.586
175
P HRP006 Herpes Simplex 65 3.585
176
PRT058 Pure Autonomic Failure 58 3.582
177
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 3.565
178
IMP005 Impotence 52 3.565
179
CNT105 Central Core Disease of Muscle 59 3.563
180
PPL052 Papillomatosis, Confluent and Reticulated 34 3.560
181
OVR094 Ovarian Epithelial Cancer 39 3.560
182
OCL069 Ocular Motor Apraxia 57 3.557
183
ANR007 Anorexia Nervosa 60 3.555
184
CNG034 Congestive Heart Failure 69 3.543
185
CRD132 Cardiac Conduction Defect 60 3.540
186
PST028 Post-Traumatic Stress Disorder 59 3.520
187
P PRS038 Personality Disorder 65 3.519
188
P END044 Endometriosis 62 3.515
189
GNR004 Generalized Anxiety Disorder 55 3.515
190
NRL016 Neural Tube Defects 81 3.506
191
P ALP061 Alopecia, Androgenetic, 1 49 3.498
192
CRB039 Cerebrovascular Disease 66 3.445
193
P TRN020 Turner Syndrome 67 3.435
194
SFT003 Soft Tissue Sarcoma 57 3.393
195
LPD008 Lipid Metabolism Disorder 62 3.375
196
P ANR048 Aniridia 1 64 3.373
197
SDD001 Sudden Infant Death Syndrome 60 3.366
198
ADN018 Adenoma 59 3.364
199
c HPT003 Hepatitis a 63 3.362
200
P PHC003 Pheochromocytoma 69 3.357
201
ADR040 Adrenal Gland Pheochromocytoma 46 3.357
202
P MLT020 Multiple Sclerosis 79 3.347
203
P FBR017 Fibrosarcoma 56 3.329
204
P LNG064 Lung Cancer Susceptibility 3 70 3.329
205
P PLM037 Pulmonary Hypertension 72 3.322
206
P HPT023 Hepatocellular Carcinoma 96 3.314
207
SCH012 Schizoaffective Disorder 50 3.280
208
c TYP008 Type 1 Diabetes Mellitus 70 3.278
209
SYN036 Syncope 45 3.245
210
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.228
211
DFC004 Deficiency Anemia 74 3.221
212
ACT240 Actn3 Deficiency 25 3.220
213
c SPL067 Split-Hand/foot Malformation 1 46 3.213
214
ISL121 Isolated Split Hand-Split Foot Malformation 41 3.213
215
APN008 Apnea, Obstructive Sleep 67 3.211
216
P DDN001 Duodenal Ulcer 53 3.203
217
HYP188 Hypnic Headache 20 3.185
218
BNR002 Bone Resorption Disease 47 3.172
219
NPH009 Nephrolithiasis 54 3.172
220
PNC129 Pancreatic Adenocarcinoma 65 3.159
221
CMM005 Common Cold 56 3.137
222
P RHM011 Rheumatoid Arthritis 82 3.136
223
PRT038 Protein-Energy Malnutrition 53 3.128
224
PRP027 Peripheral Vascular Disease 71 3.122
225
CYS001 Cystic Fibrosis 78 3.119
226
SKN019 Skin Melanoma 71 3.117
227
DNT012 Dental Caries 53 3.115
228
NRM005 Neuromuscular Disease 63 3.112
229
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.092
230
P PNC035 Pancreatic Cancer 86 3.091
231
c HYP836 Hypercholesterolemia, Familial, 1 73 3.086
232
INT002 Intermittent Claudication 61 3.080
233
CLT003 Colitis 63 3.078
234
c ACT027 Acute Pancreatitis 60 3.021
235
PPT005 Peptic Ulcer Disease 58 3.005
236
HMN044 Human Immunodeficiency Virus Type 1 78 3.002
237
BLR008 Bilirubin Metabolic Disorder 57 2.978
238
P PRS040 Prostate Cancer 95 2.959
239
c ACT071 Acute Kidney Failure 60 2.940
240
c HPT073 Hepatitis C Virus 71 2.940
241
P EPL164 Epilepsy 68 2.934
242
LNG099 Lung Disease 62 2.920
243
c PRX088 Paroxysmal Nonkinesigenic Dyskinesia 1 37 2.917
244
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 2.911
245
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.903
246
c BSL007 Basal Cell Carcinoma 68 2.903
247
AGR002 Agoraphobia 45 2.881
248
ADL002 Adult Syndrome 70 2.877
249
MSC157 Muscular Dystrophy, Duchenne Type 79 2.873
250
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.871
251
CNS004 Constipation 56 2.866
252
P MGR003 Migraine with Aura 52 2.849
253
ALC009 Alcoholic Liver Cirrhosis 54 2.825
254
FBR047 Fibromyalgia 58 2.819
255
PPL022 Papilloma 53 2.768
256
P DRR001 Diarrhea 55 2.767
257
ACT084 Acute Stress Disorder 54 2.761
258
CRH001 Crohn's Disease 80 2.735
259
PRT251 Proteinuria, Chronic Benign 57 2.722
260
INF118 Inflammatory Myopathy with Abundant Macrophages 27 2.722
261
c GLL024 Gallbladder Disease 1 52 2.702
262
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 2.698
263
P AST005 Asthma 76 2.666
264
P MYP006 Myopia 56 2.666
265
DSS008 Disease of Mental Health 74 2.666
266
P PNC044 Pancreatitis 61 2.657
267
HRT011 Heart Septal Defect 49 2.655
268
P VSC007 Vascular Disease 63 2.653
269
c DLT002 Dilated Cardiomyopathy 78 2.650
270
c CHR684 Chronic Kidney Disease 69 2.650
271
P ADL010 Adult Respiratory Distress Syndrome 71 2.645
272
CCN001 Cocaine Dependence 48 2.642
273
CHL014 Cholera 62 2.625
274
GST033 Gestational Diabetes 61 2.621
275
ATN005 Autonomic Dysfunction 46 2.621
276
c ACT075 Acute Myocardial Infarction 56 2.608
277
CYN002 Cyanosis, Transient Neonatal 43 2.592
278
MSC007 Muscle Hypertrophy 64 2.592
279
PRM236 Primary Biliary Cholangitis 60 2.592
280
P URN019 Urinary Tract Infection 49 2.585
281
P BND020 Bone Disease 59 2.573
282
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.573
283
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.558
284
P RCT021 Rectum Cancer 54 2.550
285
PSR001 Psoriatic Arthritis 62 2.537
286
c ATR087 Atrial Standstill 1 74 2.530
287
PRT013 Portal Hypertension 59 2.518
288
HDN002 Head Injury 44 2.518
289
CLF001 Cleft Lip 53 2.515
290
SQM002 Squamous Cell Papilloma 46 2.515
291
P MYG005 Myoglobinuria 40 2.514
292
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 2.484
293
P RTN024 Retinoblastoma 73 2.484
294
CHL068 Cholestasis 61 2.484
295
c VRL010 Viral Hepatitis 53 2.477
296
AND005 Androgen Insensitivity Syndrome, Mild 21 2.477
297
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 2.445
298
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.439
299
DSC013 Discrimination, Two-Point, Reduction in 21 2.439
300
c BRN108 Branchiootic Syndrome 1 62 2.435
301
MTN003 Motion Sickness 51 2.413
302
P MCH002 Machado-Joseph Disease 62 2.400
303
PLM010 Pulmonary Edema 55 2.393
304
P HYP061 Hypertrophic Cardiomyopathy 69 2.377
305
P ECL001 Eclampsia 52 2.377
306
SVR004 Severe Combined Immunodeficiency 72 2.377
307
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 2.373
308
PRV004 Periventricular Leukomalacia 52 2.360
309
RHB024 Rhabdomyosarcoma 2 67 2.341
310
P PRD008 Periodontitis 64 2.339
311
KRT002 Keratomalacia 55 2.337
312
P LPS004 Lupus Erythematosus 61 2.319
313
P RNL015 Renal Hypertension 45 2.319
314
ALL014 Allergic Encephalomyelitis 34 2.319
315
IMM167 Immune Deficiency Disease 78 2.309
316
OST012 Osteoarthritis 77 2.305
317
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 2.301
318
c SYS001 Systemic Lupus Erythematosus 87 2.277
319
c FNC027 Fanconi Anemia, Complementation Group a 81 2.277
320
HPT004 Hepatic Coma 43 2.277
321
ALC006 Alcoholic Hepatitis 61 2.277
322
HPT019 Hepatic Encephalopathy 59 2.277
323
P CLS010 Cluster Headache 42 2.270
324
PRX035 Paroxysmal Dyskinesia 30 2.263
325
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.263
326
BRN004 Brain Edema 54 2.263
327
RSC001 Rosacea 55 2.263
328
CLF056 Cleft Lip with or Without Cleft Palate 42 2.263
329
INT071 Intestinal Perforation 49 2.263
330
P LNG028 Long Qt Syndrome 64 2.263
331
c MLG069 Malignant Hypertension 46 2.263
332
PLC008 Placenta Disease 49 2.263
333
c HPT016 Hepatitis B 62 2.263
334
P URT039 Urticaria 58 2.260
335
MLT157 Multiple System Atrophy 1 69 2.234
336
MCN017 Meconium Ileus 53 2.230
337
DSS032 Disease by Infectious Agent 55 2.229
338
P LTH003 Lethal Congenital Contracture Syndrome 41 2.223
339
LRN003 Learning Disability 49 2.223
340
ADG002 Audiogenic Seizures 25 2.223
341
ANV001 Anovulation 47 2.223
342
PTH003 Pathologic Nystagmus 52 2.223
343
ACT133 Acetylation, Slow 20 2.209
344
CNT061 Conotruncal Heart Malformations 66 2.205
345
P HYP086 Hypothyroidism 69 2.198
346
P HYP076 Hyperthyroidism 53 2.198
347
EXR010 Exercise-Induced Bronchoconstriction 34 2.190
348
IRR002 Irritable Bowel Syndrome 65 2.186
349
PLY150 Polykaryocytosis Inducer 29 2.182
350
P ORT004 Orthostatic Intolerance 63 2.182
351
PRS021 Prostatic Adenoma 43 2.182
352
THR004 Thrombocytosis 53 2.182
353
PRS045 Prostatic Hypertrophy 53 2.182
354
STM007 Stomatitis 54 2.182
355
P HYP263 Hypersomnia 41 2.176
356
P FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 39 2.175
357
c ATS007 Autism Spectrum Disorder 72 2.154
358
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 2.144
359
INT067 Interstitial Nephritis 46 2.144
360
SVR001 Severe Acute Respiratory Syndrome 67 2.144
361
KWS001 Kwashiorkor 45 2.144
362
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.140
363
HYP014 Hyperuricemia 51 2.140
364
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.121
365
LSC001 Lesch-Nyhan Syndrome 62 2.112
366
P LKM002 Leukemia 67 2.107
367
GST009 Gastroschisis 53 2.097
368
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 13 2.097
369
PRS129 Prostatic Hyperplasia, Benign 49 2.097
370
c DMN005 Diamond-Blackfan Anemia 2 28 2.097
371
MTG002 Mutagen Sensitivity 35 2.097
372
RFR003 Refractive Error 41 2.097
373
ABD010 Abdominal Wall Defect 39 2.097
374
c HYP724 Hyperlipoproteinemia, Type Iii 67 2.096
375
INS001 Insulinoma 59 2.084
376
PRX022 Paroxysmal Choreoathetosis 23 2.079
377
P EXN002 Exanthem 58 2.053
378
ALX002 Alexithymia 37 2.053
379
P HLP001 Holoprosencephaly 69 2.053
380
END086 End Stage Renal Disease 52 2.053
381
P MYC033 Myoclonus 47 2.053
382
P RHB003 Rhabdomyosarcoma 66 2.047
383
P HYP098 Hypereosinophilic Syndrome 66 2.047
384
ATR057 Atrioventricular Block 54 2.044
385
ART002 Arts Syndrome 66 2.040
386
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.030
387
P VNT002 Ventricular Septal Defect 58 2.007
388
P ADN016 Adenocarcinoma 63 2.007
389
MCR013 Microphthalmia 60 2.007
390
P FML187 Familial Hypertension 34 2.007
391
VCC001 Vaccinia 47 1.997
392
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.988
393
CRV035 Cervical Cancer 73 1.975
394
c MCR113 Microvascular Complications of Diabetes 3 52 1.975
395
ANG054 Angina Pectoris 66 1.961
396
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.961
397
P MLN007 Male Infertility 56 1.961
398
c ACT068 Acute Cystitis 61 1.961
399
PRM003 Premature Ejaculation 44 1.961
400
THY029 Thyroid Carcinoma 51 1.959
401
ATN004 Autonomic Neuropathy 42 1.959
402
STT001 Status Epilepticus 59 1.959
403
URT049 Urate Oxidase, Pseudogene 24 1.943
404
TTH006 Tooth Disease 51 1.937
405
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.933
406
FDL002 Food Allergy 47 1.920
407
P RHN004 Rhinitis 57 1.920
408
P INT143 Interstitial Cystitis 60 1.920
409
P EPS003 Episodic Ataxia 59 1.919
410
SKN016 Skin Disease 63 1.918
411
URM002 Uremia 47 1.910
412
CMP010 Complex Regional Pain Syndrome 60 1.910
413
P GST044 Gastritis 55 1.910
414
BRX001 Bruxism 51 1.910
415
NRL004 Neuroleptic Malignant Syndrome 52 1.910
416
P TMP001 Temporal Lobe Epilepsy 49 1.910
417
INF043 Infantile Apnea 21 1.910
418
DVR002 Diverticulitis 46 1.910
419
ULC004 Ulcerative Colitis 74 1.907
420
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.904
421
c MLG084 Malignant Fibrous Histiocytoma 62 1.888
422
CRN030 Coronary Stenosis 50 1.874
423
AMN001 Amenorrhea 54 1.874
424
SPL018 Splenomegaly 49 1.874
425
THR024 Thrombosis 56 1.861
426
END040 Endogenous Depression 55 1.861
427
P ANP001 Anaplastic Large Cell Lymphoma 61 1.859
428
DNT001 Dental Fluorosis 43 1.859
429
CLL003 Cellulitis 53 1.842
430
INT003 Intracranial Hypotension 36 1.838
431
ATX019 Ataxia with Vitamin E Deficiency 44 1.835
432
GST019 Gastrointestinal Stromal Tumor 78 1.834
433
STN005 St Anthony's Fire 18 1.828
434
HYP540 Hypertension, Diastolic 37 1.828
435
P GST053 Gastric Cancer 83 1.828
436
c EPS035 Episodic Ataxia, Type 2 63 1.816
437
ANT078 Antipyrine Metabolism 23 1.806
438
RNL077 Renal Fibrosis 46 1.806
439
P BCL017 B-Cell Lymphoma 59 1.806
440
P ESP024 Esophagitis 60 1.806
441
GST023 Gastric Ulcer 52 1.806
442
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.805
443
P MYT002 Myotonic Dystrophy 51 1.799
444
c SML038 Small Cell Cancer of the Lung 69 1.797
445
c ACT134 Acute Liver Failure 59 1.781
446
ANN002 Anencephaly 57 1.781
448
P FTL001 Fetal Alcohol Syndrome 55 1.781
449
ENM002 Enamel Erosion 25 1.781
450
DNT008 Denture Stomatitis 35 1.781
451
CRN019 Coronary Artery Vasospasm 47 1.767
452
P DYS154 Dystonia 64 1.766
453
P CRD246 Cardiovascular System Disease 56 1.760
454
BNG077 Benign Idiopathic Neonatal Seizures 23 1.751
455
OBN001 Ouabain Resistance 16 1.751
456
MSC152 Muscular Dystrophy, Becker Type 69 1.751
457
P LKM071 Leukemia, Chronic Lymphocytic 75 1.751
458
LNG030 Lung Adenoma 37 1.751
459
PRP016 Paraplegia 52 1.751
460
HMS001 Hemosiderosis 48 1.751
461
P ANG015 Angioedema 56 1.751
462
TST018 Testicular Yolk Sac Tumor 39 1.751
463
P END039 Endodermal Sinus Tumor 41 1.751
464
CRB090 Cerebral Hypoxia 42 1.751
465
HYP264 Hypertonia 36 1.751
466
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 1.734
467
P NTR004 Neutropenia 63 1.734
468
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.732
469
CHR005 Chorioamnionitis 50 1.732
470
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.732
471
INT060 Intestinal Atresia 41 1.732
472
P ATR010 Atrial Heart Septal Defect 58 1.732
473
HGH043 High Grade Glioma 45 1.732
474
P BNG032 Benign Mesothelioma 53 1.732
475
ORL011 Oral Cancer 60 1.732
476
BDR001 Bidirectional Tachycardia 14 1.732
477
c BLD140 Blood Group, I System 46 1.725
478
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 1.725
479
VTM033 Vitamin K Deficiency Bleeding 48 1.720
480
GRW007 Growth Hormone Deficiency 46 1.719
481
ALL003 Allergic Rhinitis 67 1.701
482
P RRH023 Rare Hereditary Hemochromatosis 54 1.692
483
QDR001 Quadriplegia 50 1.692
484
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.691
485
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 1.691
486
NWB001 Newborn Respiratory Distress Syndrome 56 1.691
487
RSP007 Respiratory Distress Syndrome, Infant 40 1.691
488
P MYS005 Myositis 56 1.681
489
HYP017 Hypophosphatemia 49 1.681
490
P OMP004 Omphalocele 48 1.681
491
P TTR001 Tetralogy of Fallot 69 1.681
492
MCR103 Microtia 44 1.681
493
DBT010 Diabetic Neuropathy 54 1.681
494
AVD001 Avoidant Personality Disorder 49 1.681
495
P CRN037 Craniosynostosis 68 1.681
496
ESP020 Esophageal Atresia 60 1.681
497
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.681
498
P ENC008 Encephalocele 46 1.681
500
P ATS364 Autism 69 1.663
501
P NJM001 Nijmegen Breakage Syndrome 76 1.663
502
ING001 Inguinal Hernia 59 1.663
503
NRT001 Neurotic Disorder 56 1.663
504
PLM033 Pulmonary Embolism 58 1.663
505
SPN340 Spontaneous Intracranial Hypotension 27 1.652
506
P CYS018 Cystitis 59 1.652
507
CHR178 Chromosomal Triplication 34 1.630
508
EXN003 Exencephaly 30 1.630
509
c MCR130 Microvascular Complications of Diabetes 6 41 1.627
510
c HNT011 Huntington Disease-Like 3 34 1.627
511
c MCR120 Microvascular Complications of Diabetes 7 47 1.627
512
c HNT004 Huntington Disease-Like 2 52 1.627
513
c MCR133 Microvascular Complications of Diabetes 4 41 1.627
514
P MCR010 Microcephaly 60 1.627
515
BRN024 Bronchitis 67 1.627
516
P RTN018 Retinal Disease 53 1.627
517
EMB004 Embryonal Carcinoma 56 1.627
518
P ART005 Arteriovenous Malformation 65 1.627
519
CND002 Conduct Disorder 51 1.627
520
c FML001 Familial Atrial Fibrillation 65 1.584
521
PLP001 Pulpitis 48 1.582
522
DRM006 Dermatitis 62 1.580
523
c MCR115 Microvascular Complications of Diabetes 5 65 1.572
524
ACT098 Acute Erythroid Leukemia 55 1.572
525
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.572
526
P MDL005 Medulloblastoma 75 1.572
527
CMB007 Combined Immunodeficiency 57 1.572
528
PRT029 Parathyroid Adenoma 51 1.572
529
PLS007 Plasmodium Falciparum Malaria 52 1.572
530
IRN002 Iron Metabolism Disease 57 1.572
531
MYT011 Myotonia 39 1.572
532
NWC001 Newcastle Disease 47 1.564
533
END072 Endotheliitis 36 1.536
534
P HMN038 Human Coronavirus Sensitivity 30 1.536
535
c LKM061 Leukemia, Acute Myeloid 83 1.514
536
INS024 Insulin-Like Growth Factor I 78 1.513
537
HMC014 Homocysteinemia 52 1.513
538
P CLC063 Celiac Disease 1 66 1.513
539
P SPP010 Suppressor of Tumorigenicity 3 51 1.513
540
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 1.513
541
P HYP750 Hypertriglyceridemia, Familial 62 1.513
542
c FBR070 Febrile Seizures, Familial, 8 44 1.513
543
HPT009 Hepatopulmonary Syndrome 48 1.513
544
MLT001 Multiple Chemical Sensitivity 39 1.513
545
SCR011 Scrapie 39 1.513
546
HRT012 Heart Valve Disease 53 1.513
547
P CCK001 Cockayne Syndrome 68 1.513
548
ANS004 Anisometropia 31 1.513
549
MYL031 Myeloproliferative Neoplasm 66 1.513
550
P PRN023 Prion Disease 60 1.513
551
SYS003 Systolic Heart Failure 49 1.513
552
PRS063 Paresthesia 39 1.513
553
P MJR007 Major Affective Disorder 1 42 1.501
554
PLL012 Pollen Allergy 45 1.494
555
CLR017 Clear Cell Sarcoma 44 1.494
556
P OBS001 Obstructive Jaundice 48 1.494
557
SPS057 Spasticity 42 1.488
558
P MYS003 Myasthenia Gravis 68 1.451
559
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.451
560
c SLV029 Silver-Russell Syndrome 2 26 1.451
561
PRG003 Progesterone-Receptor Negative Breast Cancer 29 1.451
562
SXL003 Sexual Disorder 49 1.451
563
WRN001 Werner Syndrome 69 1.451
564
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 1.451
565
c XRD032 Xeroderma Pigmentosum, Complementation Group B 50 1.451
566
INC002 Inclusion Body Myositis 57 1.451
567
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 1.451
568
MMM006 Mammographic Density 39 1.451
569
P GLL020 Gallbladder Disease 56 1.451
570
P FBR003 Fibrous Histiocytoma 43 1.451
571
CNN001 Cannabis Dependence 38 1.451
572
P SNS001 Sensorineural Hearing Loss 59 1.451
573
OCL010 Ocular Hypotension 37 1.451
574
P TCD001 Tic Disorder 49 1.451
575
P MYC008 Myocarditis 59 1.451
576
P PRP029 Porphyria 60 1.417
577
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 55 1.417
578
P CNR004 Cone-Rod Dystrophy 2 74 1.406
579
CNT017 Central Nervous System Origin Vertigo 44 1.406
580
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.406
581
PRS047 Prostatitis 58 1.402
582
LPT006 Leptin Receptor Deficiency 50 1.400
583
FRC013 Fructose Utilization 15 1.386
584
NRL025 Neural Tube Closure Defect 27 1.386
585
DGT004 Digitalis Poisoning 13 1.386
586
SRC027 Sarcoma, Synovial 58 1.386
587
P FML023 Familial Hemiplegic Migraine 53 1.386
588
P CRG003 Crigler-Najjar Syndrome, Type I 63 1.386
589
c FNC042 Fanconi Anemia, Complementation Group D2 54 1.386
590
PLY001 Polycythemia Vera 69 1.386
591
ESP021 Esophageal Cancer 83 1.386
592
MDD018 Middle East Respiratory Syndrome 44 1.386
593
PST092 Posttransplant Acute Limbic Encephalitis 28 1.386
594
P PLY018 Polycythemia 56 1.386
595
RTN003 Retinal Ischemia 49 1.386
596
DMP001 Dumping Syndrome 43 1.386
597
DRG002 Drug-Induced Hepatitis 42 1.386
598
P EYD002 Eye Disease 57 1.386
599
EXT006 Extrahepatic Cholestasis 40 1.386
600
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.386
601
DVL001 Developmental Coordination Disorder 34 1.386
602
P TRC031 Trichorhinophalangeal Syndrome 38 1.386
603
P FBR031 Febrile Seizures 52 1.386
604
DVL005 Developmental Dyspraxia 22 1.386
605
NN2002 Non 24 Hour Sleep Wake Disorder 24 1.386
606
NND010 Nondisjunction 34 1.372
607
P MSC003 Muscular Atrophy 52 1.368
608
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 1.366
609
ANT039 Antisynthetase Syndrome 55 1.366
610
DYS140 Dyskinesia, Familial, with Facial Myokymia 37 1.337
611
PYR009 Pyridoxine Deficiency Anemia 35 1.331
612
PSD088 Pseudobulbar Affect 33 1.331
613
ART074 Aortic Dissection 53 1.315
614
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.315
615
HRN029 Hearing Loss, Noise-Induced 37 1.315
616
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.315
617
RTR008 Root Resorption 44 1.315
618
P BRS053 Breast Fibroadenoma 49 1.315
619
IRN001 Iron Deficiency Anemia 58 1.315
620
P PTS002 Ptosis 52 1.315
621
FNC002 Functional Diarrhea 40 1.315
622
IMM002 Immature Cataract 28 1.315
623
P MYL006 Myeloid Leukemia 61 1.302
624
P OPT006 Optic Nerve Disease 58 1.302
625
STR067 Stroke, Ischemic 80 1.302
626
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.302
627
P GLM040 Glioma Susceptibility 1 71 1.300
628
MLG169 Malignant Astrocytoma 57 1.300
629
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 1.297
630
MTC005 Mitochondrial Metabolism Disease 45 1.287
631
P MTR014 Motor Neuron Disease 65 1.287
632
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 1.249
633
GST050 Gastrointestinal System Disease 55 1.249
634
CHR073 Choreatic Disease 54 1.249
635
MTB016 Metabolic Myopathy 30 1.238
636
c SPR086 Spermatogenic Failure 3 46 1.238
637
ATM095 Autoimmune Disease 61 1.238
638
ACT088 Acute Insulin Response 39 1.238
639
P CRP001 Carpal Tunnel Syndrome 66 1.238
640
DBT084 Diabetes Mellitus, Ketosis-Prone 60 1.238
641
BNS007 Bone Sarcoma 51 1.238
642
GST040 Gastric Adenocarcinoma 67 1.238
643
RTR001 Retrograde Amnesia 41 1.238
644
CRD005 Cardia Cancer 38 1.238
645
SPR017 Spermatocele 36 1.238
646
MRS001 Marasmus 42 1.238
647
MYM001 Myoma 54 1.238
648
CLN015 Colon Adenocarcinoma 65 1.238
649
HPT014 Hepatorenal Syndrome 49 1.238
650
P HYP040 Hypospadias 51 1.238
651
PLM028 Pulmonary Coin Lesion 30 1.238
652
PLM031 Poliomyelitis 63 1.238
653
CRT015 Carotid Artery Occlusion 45 1.238
654
P CYS039 Cystic Kidney Disease 53 1.238
655
TRP014 Triploidy 38 1.238
656
c LCL022 Localized Lipodystrophy 32 1.238
657
c SPN330 Spondylocostal Dysostosis 5 54 1.237
658
CRB009 Cerebritis 43 1.237
659
c PSR028 Psoriasis 7 43 1.236
660
c PSR017 Psoriasis 2 53 1.236
661
c PSR018 Psoriasis 13 52 1.236
662
c PSR023 Psoriasis 1 52 1.236
663
c PSR032 Psoriasis 11 47 1.236
664
P MTH007 Methemoglobinemia 46 1.235
665
LYM019 Lymphosarcoma 46 1.235
666
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.231
667
P ACN011 Acne 57 1.231
668
P INF038 Influenza 68 1.231
669
RCK004 Rickets 68 1.231
670
OPT003 Opiate Dependence 49 1.231
671
P CNJ013 Conjunctivitis 66 1.231
672
c SPN225 Spondyloarthropathy 1 70 1.222
673
c FNC043 Fanconi Anemia, Complementation Group E 62 1.222
674
c PNT034 Pontocerebellar Hypoplasia, Type 2e 52 1.222
675
c PNT049 Pontocerebellar Hypoplasia, Type 2d 43 1.222
676
NRR001 Neuroretinitis 42 1.222
677
RTN023 Retinitis 46 1.222
678
DWR001 Dwarfism 44 1.209
679
P INF037 Inflammatory Bowel Disease 53 1.196
680
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 64 1.196
681
P CNT009 Central Core Myopathy 43 1.196
682
VSC002 Vascular Dementia 60 1.196
683
P PLM036 Pulmonary Fibrosis 66 1.154
684
ACQ007 Acquired Immunodeficiency Syndrome 59 1.154
685
OLG003 Oligohydramnios 51 1.154
686
NTR005 Nutritional Deficiency Disease 61 1.153
687
SRT004 Serotonin Syndrome 54 1.153
688
c THY107 Thymoma, Familial 42 1.153
689
c CHR579 Chiari Malformation Type Ii 44 1.153
690
DFF005 Diffuse Large B-Cell Lymphoma 54 1.153
691
UMB002 Umbilical Hernia 47 1.153
692
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 22 1.153
693
c MCR312 Microphthalmia, Syndromic 10 40 1.153
694
BLM001 Bloom Syndrome 65 1.153
695
P PRR016 Pierre Robin Syndrome 50 1.153
696
GLB001 Gilbert Syndrome 53 1.153
697
DBT006 Diabetic Macular Edema 48 1.153
698
HYP034 Hypertensive Encephalopathy 43 1.153
699
CLR003 Clear Cell Adenocarcinoma 50 1.153
700
PLR008 Pleurisy 50 1.153
701
TRN018 Transitional Cell Carcinoma 56 1.153
702
P PLY011 Polycystic Ovary Syndrome 57 1.153
703
MCL006 Macular Retinal Edema 57 1.153
704
P THY023 Thymoma 64 1.153
705
DPR002 Depersonalization Disorder 41 1.153
706
HYP835 Hypothalamic Obesity 38 1.153
707
CRT057 Critical Congenital Heart Disease 21 1.153
708
P CHR342 Chiari Malformation 41 1.153
709
EXR008 Exercise-Induced Malignant Hyperthermia 20 1.140
710
P NRP001 Neuropathy 60 1.140
711
c SVR005 Severe Pre-Eclampsia 50 1.140
712
P HYP265 Hypotonia 42 1.140
713
CRH005 Crohn's Colitis 53 1.117
714
P ART021 Arteriosclerosis 54 1.108
715
URL001 Urolithiasis 46 1.082
716
P LKM062 Leukemia, Acute Lymphoblastic 69 1.082
717
RMS001 Rem Sleep Behavior Disorder 47 1.082
718
LYM133 Lymphoma, Hodgkin, Classic 74 1.056
719
c LKM063 Leukemia, Chronic Myeloid 71 1.056
720
P LYM118 Lymphoma 67 1.056
721
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.056
722
c HYD064 Hydrocephalus, Congenital, 1 51 1.056
723
CHR619 Chromosome 2q35 Duplication Syndrome 64 1.056
724
HRN026 Hernia, Hiatus 47 1.056
725
AVN001 Avian Influenza 61 1.056
726
P CHL066 Cholangitis 52 1.056
727
P PTT006 Pituitary Adenoma 55 1.056
728
TRT001 Teratocarcinoma 42 1.056
729
MTS001 Mutism 44 1.056
730
CRB004 Cerebral Artery Occlusion 45 1.056
731
CHL004 Cholelithiasis 49 1.056
732
SML003 Small Cell Osteogenic Sarcoma 25 1.056
733
OLG001 Oligospermia 45 1.056
734
P SCL048 Sclerosteosis 58 1.056
735
ANK001 Ankylosis 51 1.056
736
DSM007 Desmoplastic Small Round Cell Tumor 54 1.056
737
PST021 Postpartum Depression 50 1.020
738
THP006 Theophylline Biotransformation 10 1.020
739
ATS010 Autosomal Recessive Disease 42 1.020
740
PTH002 Pathological Gambling 48 1.020
741
DYS009 Dysthymic Disorder 52 1.020
742
TXC005 Toxic Shock Syndrome 62 1.020
743
TST014 Testicular Cancer 52 1.020
744
SCL003 Social Phobia 48 1.020
745
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 39 1.020
747
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.977
748
P MYC084 Mycobacterium Tuberculosis 1 68 0.973
749
MLR004 Malaria 80 0.973
750
CVD001 Covid-19 57 0.973
751
c INH020 Inherited Metabolic Disorder 48 0.973
752
P FML011 Familial Adenomatous Polyposis 71 0.971
753
CRN270 Coronary Artery Dissection, Spontaneous 32 0.971
754
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 0.971
755
c DRM054 Dermatitis, Atopic, 2 46 0.955
756
TRD006 Tardive Dyskinesia 53 0.954
757
c PCH010 Pachyonychia Congenita 3 43 0.954
758
ARG004 Argyria 26 0.954
759
TRN015 Transient Cerebral Ischemia 63 0.954
760
P PRP019 Peripheral Nervous System Disease 58 0.954
761
RYN005 Raynaud Phenomenon 45 0.954
762
c GRV008 Graves Disease 1 54 0.941
763
TRG002 Trigeminal Neuralgia 61 0.941
764
c WLM013 Wilms Tumor 1 66 0.941
765
FCT008 Factitious Disorder 34 0.941
766
P NLD001 Nail Disease 51 0.941
767
PLS011 Plasmacytoma 56 0.941
768
GST007 Gastric Dilatation 30 0.941
769
P MYT023 Myotonia Congenita 55 0.941
770
JPN002 Japanese Encephalitis 61 0.941
771
AMP007 Amphetamine Abuse 36 0.941
772
NRN002 Neuronitis 31 0.937
773
c MLG151 Malignant Hyperthermia 5 27 0.894
774
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.883
775
P GLC113 Galactosemia I 66 0.883
776
BTT016 Batten-Turner Congenital Myopathy 53 0.883
777
PHN003 Phenylketonuria 76 0.883
778
LMY002 Leiomyoma 51 0.883
779
PRD002 Periodic Limb Movement Disorder 34 0.883
780
TXC002 Toxic Encephalopathy 52 0.883
781
P PRD021 Periodic Paralysis 41 0.883
782
P LCT001 Lactic Acidosis 51 0.883
783
P UVT001 Uveitis 57 0.883
784
NRG002 Neurogenic Bladder 55 0.883
785
P HYP069 Hyperparathyroidism 62 0.883
786
ALL009 Allergic Conjunctivitis 51 0.883
787
CRB079 Cerebrospinal Fluid Leak 35 0.883
788
SPP007 Suppression Amblyopia 38 0.874
789
AMB002 Amblyopia 50 0.874
790
c PRX024 Paroxysmal Nonkinesigenic Dyskinesia 2 18 0.862
791
c THR092 Thrombophilia Due to Thrombin Defect 74 0.858
792
P PLV020 Pelvic Organ Prolapse 58 0.858
793
P MCR129 Microvascular Complications of Diabetes 1 68 0.858
794
P THL005 Thalassemia 56 0.806
795
P OVR082 Overgrowth Syndrome 49 0.806
796
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.806
797
PRM329 Premature Aging 36 0.806
798
NPH003 Nephrocalcinosis 49 0.806
799
c FML191 Familial Long Qt Syndrome 55 0.806
800
TLG001 Telogen Effluvium 31 0.806
801
CNN005 Connective Tissue Disease 67 0.806
802
MRP001 Morphine Dependence 42 0.806
803
PPT001 Peptic Esophagitis 52 0.806
804
OPD006 Opioid Addiction 48 0.806
805
DYS073 Dysphagia 53 0.806
806
NWD001 New Daily-Persistent Headache 20 0.806
807
ANG049 Angioedema Induced by Ace Inhibitors 40 0.792
808
AYM001 Ayme-Gripp Syndrome 56 0.792
809
c OVR114 Ovarian Cancer 1 59 0.792
810
c GLC078 Glaucoma 1, Open Angle, F 34 0.792
811
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.792
812
PRP083 Porphyria, Acute Intermittent 65 0.792
813
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.792
814
PRP082 Porphyria, Congenital Erythropoietic 56 0.792
815
CPR004 Coproporphyria, Hereditary 57 0.792
816
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 58 0.792
817
ACT055 Actinomycosis 55 0.792
818
c DRR009 Diarrhea 6 45 0.792
819
ACT078 Acute Porphyria 49 0.792
820
OBS003 Obsessive-Compulsive Personality Disorder 43 0.792
821
VST004 Vestibular Disease 40 0.792
822
CTN011 Cutaneous Porphyria 45 0.792
823
PRR004 Preretinal Fibrosis 34 0.792
824
NRN004 Neuroendocrine Tumor 59 0.792
825
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.792
826
c CHR064 Chronic Monocytic Leukemia 36 0.792
827
P RRT020 Rare Tumor 39 0.792
828
P RTT002 Rett Syndrome 79 0.792
829
LMB010 Lambert Syndrome 30 0.792
830
MNN032 Meningococcal Meningitis 53 0.792
831
DSN001 De Sanctis-Cacchione Syndrome 36 0.792
832
KRT019 Keratitis, Hereditary 66 0.792
833
c TRC073 Treacher Collins Syndrome 2 26 0.792
834
c SCH079 Schizophrenia 1 44 0.792
835
c CLR066 Ciliary Dyskinesia, Primary, 2 40 0.792
836
NSL006 Nasal Cavity Squamous Cell Carcinoma 28 0.792
837
P MLG074 Malignant Mesenchymoma 40 0.792
838
CRC021 Carcinosarcoma 64 0.792
839
PLM030 Pleomorphic Rhabdomyosarcoma 40 0.792
840
P EXT032 Extraosseous Osteosarcoma 31 0.792
841
BLD131 Bladder Urothelial Carcinoma 60 0.792
842
PRT036 Peritonitis 65 0.792
843
GRN004 Granulomatous Amebic Encephalitis 30 0.792
844
P SLF001 Sulfhemoglobinemia 23 0.792
845
P LMY004 Leiomyosarcoma 62 0.792
846
P MNN013 Meningitis 65 0.792
847
P ENC004 Encephalitis 61 0.792
848
P NRV007 Nervous System Disease 67 0.780
849
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 43 0.779
850
PRX087 Paroxysomal Nonkinesigenic Dyskinesia 2 0.779
851
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.777
852
CHR682 Chronic Bilirubin Encephalopathy 37 0.777
853
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.777
854
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.777
855
c ORT011 Orthostatic Hypotension 1 43 0.777
856
P THR117 Three M Syndrome 1 65 0.777
857
c PRS136 Prostate Cancer, Hereditary, 6 33 0.777
858
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.777
859
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 0.777
860
PRG017 Paraganglioma and Gastric Stromal Sarcoma 63 0.777
861
c PRS130 Prostate Cancer, Hereditary, 8 32 0.777
862
ISL003 Isolated Growth Hormone Deficiency 57 0.777
863
P MTC069 Mitochondrial Disorders 57 0.777
864
c PRM038 Primary Agammaglobulinemia 47 0.777
865
CHL079 Children's Interstitial Lung Disease 26 0.777
866
PLY100 Polyploidy 36 0.721
867
ACT235 Acute Macular Neuroretinopathy 16 0.721
868
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.721
869
P DPY001 Dupuytren Contracture 39 0.721
870
c PRG042 Progressive Familial Heart Block, Type Ia 66 0.721
871
c BTT014 Beta-Thalassemia 72 0.721
872
BRR014 Barrett Esophagus 66 0.721
873
c CHR711 Chronic Asthma 41 0.721
874
CLR108 Colorectal Adenoma 64 0.721
875
HLC007 Helicobacter Pylori Infection 67 0.721
876
EXF001 Exfoliation Syndrome 56 0.721
877
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 0.721
878
VRC005 Varicose Veins 60 0.721
879
c SZR022 Seizures, Benign Familial Neonatal, 1 43 0.721
880
CHL065 Cholangiocarcinoma 58 0.721
881
P SCL018 Scoliosis 57 0.721
882
P LCT002 Lactose Intolerance 52 0.721
883
PNM008 Pneumothorax 54 0.721
884
MYF001 Myofibroma 42 0.721
885
P GRF003 Graft-Versus-Host Disease 71 0.721
886
ASP007 Aspiration Pneumonia 49 0.721
887
ANG020 Angiosarcoma 64 0.721
888
ACR007 Acromegaly 70 0.721
889
CRV040 Cervix Carcinoma 50 0.721
890
DBL002 Double Outlet Right Ventricle 57 0.721
891
INT079 Intrahepatic Cholangiocarcinoma 51 0.721
892
P BLP003 Blepharospasm 46 0.721
893
ANT019 Anterograde Amnesia 38 0.721
894
ENT004 Enthesopathy 51 0.721
895
ALB002 Albinism 47 0.721
896
GRN017 Granulocytopenia 42 0.721
897
BRK012 Broken Heart Syndrome 42 0.721
898
c MYT021 Myotonic Dystrophy 1 68 0.709
899
LMB062 Limb Ischemia 55 0.709
900
c DYS119 Dystonia 9 52 0.709
901
HND015 Hand Skill, Relative 30 0.709
902
NSP002 Nasopharyngitis 45 0.709
903
DNG003 Dengue Disease 65 0.709
904
GTR002 Goiter 53 0.709
905
P INT068 Intestinal Disease 53 0.709
906
OPD001 Opioid Abuse 44 0.709
907
P NRF002 Neurofibromatosis 57 0.709
908
NRF007 Neurofibroma 64 0.709
909
P SCK005 Sickle Cell Disease 56 0.709
910
P SKL032 Skeletal Muscle Disease 25 0.624
911
THN005 Thunderclap Headache 15 0.624
912
P LPR021 Leprosy 3 71 0.624
913
BLP048 Blepharospasm, Benign Essential 37 0.624
914
c RTN047 Retinitis Pigmentosa 18 46 0.624
915
CRT045 Creatine Phosphokinase, Elevated Serum 39 0.624
916
GLL008 Gilles De La Tourette Syndrome 65 0.624
917
VTM002 Vitamin B12 Deficiency 48 0.624
918
DLY008 Delayed Sleep Phase Disorder 44 0.624
919
MYL020 Myelomeningocele 51 0.624
920
VRG001 Variegate Porphyria 56 0.624
921
EWN003 Ewing Sarcoma 70 0.624
922
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.624
923
P SRC025 Sarcoidosis 1 71 0.624
924
P EPS030 Episodic Kinesigenic Dyskinesia 1 55 0.624
925
ISL151 Isolated Elevated Serum Creatine Phosphokinase Levels 39 0.624
926
c ACT073 Acute Leukemia 58 0.624
927
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.624
928
SCT002 Scotoma 42 0.624
929
INT075 Intracranial Hypertension 53 0.624
930
ALL006 Allergic Asthma 56 0.624
931
P ATR005 Atrophic Gastritis 50 0.624
932
CHR074 Choriocarcinoma 46 0.624
933
CHR066 Chronic Fatigue Syndrome 60 0.624
934
PRX097 Paroxysmal Dystonia 32 0.624
935
P ALP009 Alopecia Areata 59 0.624
936
CHL067 Cholecystitis 60 0.624
937
P CND004 Candidiasis 58 0.624
938
P LNG035 Lung Large Cell Carcinoma 54 0.624
939
CHL061 Childhood Leukemia 47 0.624
940
DLS001 Delusional Disorder 45 0.624
941
P PLL002 Pellagra 46 0.624
942
OST011 Osteomalacia 52 0.624
943
c SCN007 Secondary Hyperparathyroidism 51 0.624
944
RFL002 Reflex Epilepsy 41 0.624
945
SNS003 Sensory Peripheral Neuropathy 52 0.624
946
RTN020 Retinal Vascular Disease 46 0.624
947
P GCH001 Gaucher's Disease 70 0.624
948
P ESS003 Essential Thrombocythemia 69 0.624
949
CHL013 Cholecystolithiasis 37 0.624
950
DSS009 Disseminated Intravascular Coagulation 57 0.624
951
c HMG003 Hemoglobin E Disease 42 0.624
952
PTT009 Pituitary Gland Disease 53 0.624