Search results for Caffeine

940 hits were found for Caffeine

# Family MCID Name MIFTS Score
1
APN006 Apnea of Prematurity 24 0.279
2
P HDC001 Headache 57 0.265
3
c MGR028 Migraine with or Without Aura 1 67 0.225
4
P MLG056 Malignant Hyperthermia 67 0.214
5
BRN056 Bronchopulmonary Dysplasia 57 0.195
6
ANX010 Anxiety 73 0.172
7
P LVR013 Liver Disease 68 0.170
8
P TRM003 Tremor 54 0.166
9
CYT018 Cytochrome P450 2d6 Variant 27 0.166
10
P SZR006 Seizure Disorder 56 0.163
11
VSL002 Visual Epilepsy 59 0.157
12
48X005 48,xyyy 39 0.155
13
c PNS012 Paine Syndrome 61 0.147
14
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.147
15
HYP266 Hypoxia 57 0.141
16
WTH001 Withdrawal Disorder 48 0.138
17
LVR012 Liver Cirrhosis 62 0.134
18
PNG002 Pain Agnosia 51 0.130
19
P PRK057 Parkinson Disease, Late-Onset 78 0.126
20
ISC004 Ischemia 58 0.126
21
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.126
22
P PNC025 Panic Disorder 53 0.124
23
OST159 Osteogenic Sarcoma 66 0.122
24
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.122
25
P ATX030 Ataxia-Telangiectasia 82 0.118
26
PSY004 Psychotic Disorder 67 0.118
27
TLN003 Telangiectasis 52 0.118
28
P PTN014 Patent Ductus Arteriosus 1 60 0.116
29
CRB037 Cerebral Palsy 69 0.112
30
P SKN015 Skin Carcinoma 66 0.112
31
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.110
32
P ATR011 Atrial Fibrillation 66 0.110
33
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.110
34
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.107
35
BRS051 Breast Disease 58 0.107
36
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.105
37
HYP056 Hypoglycemia 66 0.105
38
P CRN300 Coronary Heart Disease 1 63 0.105
39
DPR016 Depression 63 0.105
40
P SLP005 Sleep Disorder 59 0.105
41
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.105
42
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.105
43
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.105
44
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.105
45
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.105
46
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.105
47
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.105
48
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.105
49
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.105
50
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.105
51
P ALZ034 Alzheimer Disease 88 0.102
52
FTT001 Fatty Liver Disease 61 0.102
53
SBS004 Substance Dependence 48 0.102
54
c EXD008 Exudative Vitreoretinopathy 1 71 0.100
55
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.097
56
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.095
57
P SLP006 Sleep Apnea 69 0.095
58
LPP008 Lipoprotein Quantitative Trait Locus 62 0.095
59
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.095
60
BRN071 Brain Injury 49 0.095
61
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.095
62
P NRB001 Neuroblastoma 72 0.092
63
DWN001 Down Syndrome 70 0.092
64
ART140 Arteries, Anomalies of 52 0.092
65
ENT011 Enterocolitis 51 0.092
66
P CLR023 Colorectal Cancer 99 0.089
67
ALC007 Alcohol Dependence 66 0.089
68
P SBS003 Substance Abuse 55 0.089
69
P CRD119 Cardiac Arrest 67 0.087
70
LNG099 Lung Disease 60 0.087
71
P CTR002 Cataract 60 0.087
72
HYP005 Hypokalemia 55 0.087
73
P OVR042 Ovarian Cancer 88 0.084
74
P HRT032 Heart Disease 75 0.084
75
ATH013 Atherosclerosis Susceptibility 65 0.084
76
CLF027 Cleft Palate, Isolated 64 0.084
77
HYP066 Hyperglycemia 61 0.084
78
PRN019 Perinatal Necrotizing Enterocolitis 59 0.084
79
MNT002 Mental Depression 58 0.084
80
MLG086 Malignant Hyperthermia Susceptibility 39 0.084
81
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.084
82
ADL002 Adult Syndrome 70 0.081
83
P DBT009 Diabetes Mellitus 64 0.081
84
P ENC018 Encephalopathy 61 0.081
85
P ALC033 Alcohol Use Disorder 58 0.081
86
ATX019 Ataxia with Vitamin E Deficiency 42 0.081
87
RST023 Resting Heart Rate, Variation in 41 0.081
88
P HPT023 Hepatocellular Carcinoma 100 0.077
89
AST005 Asthma 76 0.077
90
P RSP003 Respiratory Failure 74 0.077
91
P SCH015 Schizophrenia 74 0.077
92
P MJR001 Major Depressive Disorder 68 0.077
93
P TRN020 Turner Syndrome 67 0.077
94
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.077
95
APN008 Apnea, Obstructive Sleep 64 0.077
96
c HPT001 Hepatitis C 62 0.077
97
ALL026 Allergic Hypersensitivity Disease 62 0.077
98
CCN002 Cocaine Abuse 49 0.077
99
BCK006 Back Pain 42 0.077
100
CHL079 Children's Interstitial Lung Disease 26 0.077
101
LPT014 Leptin Deficiency or Dysfunction 74 0.074
102
P OST002 Osteoporosis 74 0.074
103
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.074
104
P MYC007 Myocardial Infarction 70 0.074
105
SRC014 Sarcoma 65 0.074
106
P MVM001 Movement Disease 63 0.074
107
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.074
108
NTR005 Nutritional Deficiency Disease 62 0.074
109
BRN002 Bronchiolitis 59 0.074
110
SPN035 Spindle Cell Sarcoma 53 0.074
111
P DDN001 Duodenal Ulcer 52 0.074
112
OCL069 Ocular Motor Apraxia 51 0.074
113
TRM010 Traumatic Brain Injury 51 0.074
114
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.074
115
SBC016 Subacute Delirium 44 0.074
116
CYT002 Cytokine Deficiency 42 0.074
117
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.074
118
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.074
119
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.071
120
P KDN018 Kidney Disease 72 0.071
121
P HNT016 Huntington Disease 72 0.071
122
P MYP004 Myopathy 70 0.071
123
P DMN002 Dementia 66 0.071
124
PPL049 Papillon-Lefevre Syndrome 65 0.071
125
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.071
126
c PRC016 Pre-Eclampsia 63 0.071
127
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.071
128
P INF032 Infertility 57 0.071
129
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.071
130
P CRD246 Cardiovascular System Disease 57 0.071
131
P ALP008 Alopecia 54 0.071
132
P LTR001 Lateral Sclerosis 54 0.071
133
SPS003 Spastic Diplegia 51 0.071
134
ILS001 Ileus 51 0.071
135
47X002 47,xyy 49 0.071
136
VTM033 Vitamin K Deficiency Bleeding 48 0.071
137
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.067
138
c HYP595 Hypertension, Essential 84 0.067
139
P PNC035 Pancreatic Cancer 84 0.067
140
GLB015 Glioblastoma Multiforme 75 0.067
141
P DRM053 Dermatitis, Atopic 66 0.067
142
TTN003 Tetanus 65 0.067
143
TBC004 Tobacco Addiction 64 0.067
144
P ADN016 Adenocarcinoma 64 0.067
145
P GLM045 Glioma 63 0.067
146
P PSR002 Psoriasis 62 0.067
147
CRD223 Cardiac Arrhythmia 60 0.067
148
c ACT071 Acute Kidney Failure 60 0.067
149
HYP060 Hyperinsulinism 54 0.067
150
OCL006 Ocular Hypertension 53 0.067
151
MCN017 Meconium Ileus 52 0.067
152
PST011 Pustulosis of Palm and Sole 52 0.067
153
DRG003 Drug Dependence 47 0.067
154
AND014 Androgenic Alopecia 46 0.067
155
GLL048 Glial Tumor 45 0.067
156
P BRS047 Breast Cancer 97 0.063
157
P HPT021 Hepatitis 67 0.063
158
P HRP006 Herpes Simplex 65 0.063
159
ADN018 Adenoma 59 0.063
160
NWB001 Newborn Respiratory Distress Syndrome 58 0.063
161
SFT003 Soft Tissue Sarcoma 56 0.063
162
AMN003 Amnestic Disorder 54 0.063
163
GLC003 Glucose Intolerance 54 0.063
164
P NRC002 Narcolepsy 52 0.063
165
PRV004 Periventricular Leukomalacia 52 0.063
166
MTB004 Metabolic Acidosis 50 0.063
167
P OPN001 Open-Angle Glaucoma 49 0.063
168
P ALP061 Alopecia, Androgenetic, 1 49 0.063
169
TTH006 Tooth Disease 46 0.063
170
CYN002 Cyanosis, Transient Neonatal 45 0.063
171
P CHR345 Chronic Pain 44 0.063
172
LWC001 Low Compliance Bladder 43 0.063
173
HRW001 Hair Whorl 36 0.063
174
STR067 Stroke, Ischemic 81 0.059
175
END057 Endometrial Cancer 74 0.059
176
P CNR004 Cone-Rod Dystrophy 2 73 0.059
177
CNG034 Congestive Heart Failure 69 0.059
178
P VSC007 Vascular Disease 63 0.059
179
c GLC092 Glaucoma, Primary Open Angle 62 0.059
180
MDD011 Mood Disorder 62 0.059
181
DRM006 Dermatitis 61 0.059
182
SDD001 Sudden Infant Death Syndrome 61 0.059
183
SPN186 Spinal Cord Injury 60 0.059
184
ETN001 Eating Disorder 60 0.059
185
CRD132 Cardiac Conduction Defect 58 0.059
186
c ACT075 Acute Myocardial Infarction 57 0.059
187
NNL006 Non-Alcoholic Steatohepatitis 54 0.059
188
SCH012 Schizoaffective Disorder 50 0.059
189
CCN001 Cocaine Dependence 48 0.059
190
P RNV001 Renovascular Hypertension 48 0.059
191
c SPL067 Split-Hand/foot Malformation 1 46 0.059
192
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.059
193
PRM020 Premenstrual Tension 40 0.059
194
OVR094 Ovarian Epithelial Cancer 38 0.059
195
PPL052 Papillomatosis, Confluent and Reticulated 33 0.059
196
NRL016 Neural Tube Defects 82 0.055
197
CYS001 Cystic Fibrosis 81 0.055
198
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.055
199
c HYP836 Hypercholesterolemia, Familial, 1 73 0.055
200
P ART022 Arthritis 69 0.055
201
OBS002 Obsessive-Compulsive Disorder 68 0.055
202
PNC129 Pancreatic Adenocarcinoma 68 0.055
203
GST092 Gastroesophageal Reflux 67 0.055
204
CRB039 Cerebrovascular Disease 67 0.055
205
c RHB024 Rhabdomyosarcoma 2 67 0.055
206
P MSC005 Muscular Dystrophy 66 0.055
207
P ADL010 Adult Respiratory Distress Syndrome 65 0.055
208
GT001 Gout 64 0.055
209
MSC007 Muscle Hypertrophy 64 0.055
210
ANR007 Anorexia Nervosa 63 0.055
211
c FNC043 Fanconi Anemia, Complementation Group E 62 0.055
212
c HPT003 Hepatitis a 62 0.055
213
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.055
214
PRT058 Pure Autonomic Failure 59 0.055
215
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.055
216
P DRR001 Diarrhea 55 0.055
217
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.055
218
P ECL001 Eclampsia 50 0.055
219
LRN003 Learning Disability 49 0.055
220
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.055
221
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.055
222
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.055
223
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.055
224
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.055
225
RSP007 Respiratory Distress Syndrome, Infant 30 0.055
226
ACT240 Actn3 Deficiency 23 0.055
227
P LNG032 Lung Cancer 98 0.050
228
P PRS040 Prostate Cancer 97 0.050
229
P BLD134 Bladder Cancer 79 0.050
230
OST012 Osteoarthritis 78 0.050
231
P LNG064 Lung Cancer Susceptibility 3 78 0.050
232
SCK003 Sickle Cell Anemia 74 0.050
233
MSC157 Muscular Dystrophy, Duchenne Type 72 0.050
234
c HPT073 Hepatitis C Virus 72 0.050
235
P PHC003 Pheochromocytoma 71 0.050
236
HMN044 Human Immunodeficiency Virus Type 1 71 0.050
237
PRP027 Peripheral Vascular Disease 71 0.050
238
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.050
239
P MLN008 Melanoma 69 0.050
240
BRN024 Bronchitis 68 0.050
241
P NRV007 Nervous System Disease 66 0.050
242
c FML001 Familial Atrial Fibrillation 65 0.050
243
PRT037 Pertussis 65 0.050
244
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.050
245
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.050
246
P END044 Endometriosis 63 0.050
247
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.050
248
P PLY014 Polycystic Kidney Disease 62 0.050
249
c BRN108 Branchiootic Syndrome 1 62 0.050
250
INT002 Intermittent Claudication 61 0.050
251
PPT005 Peptic Ulcer Disease 59 0.050
252
DSS008 Disease of Mental Health 58 0.050
253
CNS004 Constipation 58 0.050
254
CMM005 Common Cold 57 0.050
255
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.050
256
P FBR017 Fibrosarcoma 56 0.050
257
c ESS001 Essential Tremor 56 0.050
258
GNR004 Generalized Anxiety Disorder 56 0.050
259
P GST044 Gastritis 56 0.050
260
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.050
261
PPL022 Papilloma 54 0.050
262
MTN003 Motion Sickness 53 0.050
263
IMP005 Impotence 52 0.050
264
END086 End Stage Renal Disease 51 0.050
265
P SCK005 Sickle Cell Disease 50 0.050
266
P MGR001 Migraine Without Aura 49 0.050
267
c SPN330 Spondylocostal Dysostosis 5 49 0.050
268
c HYD064 Hydrocephalus, Congenital, 1 48 0.050
269
ADR040 Adrenal Gland Pheochromocytoma 46 0.050
270
AGR002 Agoraphobia 45 0.050
271
c PRM038 Primary Agammaglobulinemia 44 0.050
272
c MLG147 Malignant Hyperthermia 1 43 0.050
273
TRP009 Triple X Syndrome 42 0.050
274
ANX004 Anoxia 40 0.050
275
ENT001 Enterocele 39 0.050
276
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.050
277
ACT133 Acetylation, Slow 23 0.050
278
P RHM011 Rheumatoid Arthritis 80 0.045
279
DFC004 Deficiency Anemia 70 0.045
280
c BSL007 Basal Cell Carcinoma 68 0.045
281
SKN019 Skin Melanoma 68 0.045
282
P HYD006 Hydrocephalus 66 0.045
283
c DPH024 Diaphragmatic Hernia, Congenital 63 0.045
284
c MLG084 Malignant Fibrous Histiocytoma 63 0.045
285
LPD008 Lipid Metabolism Disorder 62 0.045
286
HYD038 Hydrops Fetalis, Nonimmune 62 0.045
287
LSC001 Lesch-Nyhan Syndrome 62 0.045
288
P PRM006 Primary Biliary Cirrhosis 62 0.045
289
PSR001 Psoriatic Arthritis 61 0.045
290
P MYL006 Myeloid Leukemia 60 0.045
291
P URT039 Urticaria 58 0.045
292
BLM002 Bulimia Nervosa 57 0.045
293
BLR008 Bilirubin Metabolic Disorder 57 0.045
294
P BPL003 Bipolar Disorder 56 0.045
295
c FML035 Familial Hyperlipidemia 55 0.045
296
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.045
297
P RST001 Restless Legs Syndrome 54 0.045
298
PRT038 Protein-Energy Malnutrition 54 0.045
299
PLM010 Pulmonary Edema 54 0.045
300
CLF001 Cleft Lip 53 0.045
301
ALC009 Alcoholic Liver Cirrhosis 53 0.045
302
c GLL024 Gallbladder Disease 1 53 0.045
303
c PSR017 Psoriasis 2 53 0.045
304
c CNT035 Central Nervous System Disease 52 0.045
305
c PSR023 Psoriasis 1 52 0.045
306
P MGR003 Migraine with Aura 52 0.045
307
OPT003 Opiate Dependence 50 0.045
308
BNR002 Bone Resorption Disease 48 0.045
309
OPD006 Opioid Addiction 48 0.045
310
PLC007 Placental Abruption 48 0.045
311
HLX001 Helix Syndrome 47 0.045
312
c PSR032 Psoriasis 11 47 0.045
313
c INH020 Inherited Metabolic Disorder 47 0.045
314
c CNG216 Congenital Hydrocephalus 47 0.045
315
P MYC033 Myoclonus 46 0.045
316
SQM002 Squamous Cell Papilloma 46 0.045
317
OPD001 Opioid Abuse 46 0.045
318
SYN036 Syncope 45 0.045
319
CNT017 Central Nervous System Origin Vertigo 45 0.045
320
BSL008 Basal Ganglia Disease 43 0.045
321
DVR002 Diverticulitis 43 0.045
322
TRC097 Tracheomalacia 42 0.045
323
c PSR028 Psoriasis 7 42 0.045
324
c PSR018 Psoriasis 13 41 0.045
325
c MJR024 Major Affective Disorder 9 41 0.045
326
P PRC031 Preeclampsia/eclampsia 1 38 0.045
327
c MJR022 Major Affective Disorder 8 38 0.045
328
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.045
329
DVL001 Developmental Coordination Disorder 34 0.045
330
PRX035 Paroxysmal Dyskinesia 33 0.045
331
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.045
332
EMP011 Emphysema, Congenital Lobar 33 0.045
333
DVL005 Developmental Dyspraxia 23 0.045
334
P GST053 Gastric Cancer 83 0.039
335
c FNC027 Fanconi Anemia, Complementation Group a 81 0.039
336
MLR004 Malaria 81 0.039
337
GST019 Gastrointestinal Stromal Tumor 78 0.039
338
c ATR087 Atrial Standstill 1 75 0.039
339
CRH001 Crohn's Disease 74 0.039
340
SVR004 Severe Combined Immunodeficiency 73 0.039
341
c SPN225 Spondyloarthropathy 1 73 0.039
342
P MLT020 Multiple Sclerosis 72 0.039
343
P EPL164 Epilepsy 71 0.039
344
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.039
345
c INF071 Inflammatory Bowel Disease 1 67 0.039
346
ALL003 Allergic Rhinitis 67 0.039
347
P HYP098 Hypereosinophilic Syndrome 67 0.039
348
c SML038 Small Cell Cancer of the Lung 65 0.039
349
c DBT099 Diabetes Mellitus, Type I 65 0.039
350
NRM005 Neuromuscular Disease 64 0.039
351
ART002 Arts Syndrome 64 0.039
352
P RHB003 Rhabdomyosarcoma 63 0.039
353
CLT003 Colitis 62 0.039
354
P MCH002 Machado-Joseph Disease 62 0.039
355
P SPN046 Spinal Muscular Atrophy 62 0.039
356
ATM095 Autoimmune Disease 62 0.039
357
ALC006 Alcoholic Hepatitis 61 0.039
358
GST033 Gestational Diabetes 61 0.039
359
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.039
360
CNT105 Central Core Disease of Muscle 60 0.039
361
P VNT002 Ventricular Septal Defect 60 0.039
362
ACQ007 Acquired Immunodeficiency Syndrome 60 0.039
363
P OPT006 Optic Nerve Disease 60 0.039
364
P BND020 Bone Disease 59 0.039
365
FBR047 Fibromyalgia 58 0.039
366
IRN002 Iron Metabolism Disease 57 0.039
367
AGN016 Aging 56 0.039
368
NPH009 Nephrolithiasis 55 0.039
369
P ART021 Arteriosclerosis 54 0.039
370
SLP001 Sleeping Sickness 54 0.039
371
CLL003 Cellulitis 54 0.039
372
CRH005 Crohn's Colitis 53 0.039
373
DNT012 Dental Caries 53 0.039
374
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.039
375
c VRL010 Viral Hepatitis 52 0.039
376
ACR041 Acromelic Frontonasal Dysostosis 52 0.039
377
P RCT021 Rectum Cancer 52 0.039
378
P MSC003 Muscular Atrophy 52 0.039
379
HYP781 Hypoascorbemia 51 0.039
380
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.039
381
HRT011 Heart Septal Defect 50 0.039
382
PLP001 Pulpitis 49 0.039
383
VCC001 Vaccinia 49 0.039
384
INT067 Interstitial Nephritis 48 0.039
385
c PNT034 Pontocerebellar Hypoplasia, Type 2e 48 0.039
386
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.039
387
P RNL015 Renal Hypertension 47 0.039
388
ATN005 Autonomic Dysfunction 46 0.039
389
GRW007 Growth Hormone Deficiency 46 0.039
390
CRN019 Coronary Artery Vasospasm 46 0.039
392
c DRM054 Dermatitis, Atopic, 2 44 0.039
393
DWR001 Dwarfism 44 0.039
394
P MYG005 Myoglobinuria 44 0.039
395
c PNT049 Pontocerebellar Hypoplasia, Type 2d 43 0.039
396
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.039
397
ALL014 Allergic Encephalomyelitis 38 0.039
398
c PRX088 Paroxysmal Nonkinesigenic Dyskinesia 1 37 0.039
399
c GLC078 Glaucoma 1, Open Angle, F 35 0.039
400
NND010 Nondisjunction 34 0.039
401
BRT055 Breath-Holding Spells 30 0.039
402
URT049 Urate Oxidase, Pseudogene 25 0.039
403
DSC013 Discrimination, Two-Point, Reduction in 23 0.039
404
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.039
405
c SYS001 Systemic Lupus Erythematosus 86 0.032
406
c LKM061 Leukemia, Acute Myeloid 84 0.032
407
c DLT002 Dilated Cardiomyopathy 79 0.032
408
P LKM071 Leukemia, Chronic Lymphocytic 79 0.032
409
IMM167 Immune Deficiency Disease 78 0.032
410
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.032
411
CRV035 Cervical Cancer 76 0.032
412
ULC004 Ulcerative Colitis 73 0.032
413
P RTN024 Retinoblastoma 73 0.032
414
P FML011 Familial Adenomatous Polyposis 72 0.032
415
P HYP061 Hypertrophic Cardiomyopathy 70 0.032
416
c CHR684 Chronic Kidney Disease 70 0.032
417
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.032
418
P LKM002 Leukemia 68 0.032
419
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.032
420
P HLP001 Holoprosencephaly 67 0.032
421
P PLM037 Pulmonary Hypertension 67 0.032
422
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.032
423
P LNG028 Long Qt Syndrome 66 0.032
424
P DYS154 Dystonia 65 0.032
425
P MTR014 Motor Neuron Disease 65 0.032
426
P PRS038 Personality Disorder 65 0.032
427
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.032
428
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.032
429
PRP083 Porphyria, Acute Intermittent 64 0.032
430
P PRD008 Periodontitis 64 0.032
431
MSC152 Muscular Dystrophy, Becker Type 63 0.032
432
P THR117 Three M Syndrome 1 63 0.032
433
c ACT068 Acute Cystitis 63 0.032
434
P LMY004 Leiomyosarcoma 63 0.032
435
P ESP024 Esophagitis 62 0.032
436
P ORT004 Orthostatic Intolerance 62 0.032
437
TXC005 Toxic Shock Syndrome 62 0.032
438
MSS001 Masa Syndrome 62 0.032
439
P PRP029 Porphyria 62 0.032
440
CHL068 Cholestasis 61 0.032
441
PRG017 Paraganglioma and Gastric Stromal Sarcoma 61 0.032
442
P KDN017 Kidney Cancer 60 0.032
443
PNM010 Pneumothorax, Primary Spontaneous 60 0.032
444
HPT019 Hepatic Encephalopathy 60 0.032
445
VRC005 Varicose Veins 60 0.032
446
ING001 Inguinal Hernia 60 0.032
447
STT001 Status Epilepticus 60 0.032
448
PRT013 Portal Hypertension 59 0.032
449
THY029 Thyroid Carcinoma 59 0.032
450
SRC027 Sarcoma, Synovial 58 0.032
451
P ANP001 Anaplastic Large Cell Lymphoma 58 0.032
452
PST028 Post-Traumatic Stress Disorder 58 0.032
453
P BCL017 B-Cell Lymphoma 58 0.032
454
CMP010 Complex Regional Pain Syndrome 58 0.032
455
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.032
456
EYD002 Eye Disease 58 0.032
457
P GLL020 Gallbladder Disease 57 0.032
458
MCR013 Microphthalmia 57 0.032
459
P EXN002 Exanthem 57 0.032
460
P RHN004 Rhinitis 57 0.032
461
CPR004 Coproporphyria, Hereditary 57 0.032
462
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.032
463
AYM001 Ayme-Gripp Syndrome 57 0.032
464
P ANG015 Angioedema 57 0.032
465
PNM008 Pneumothorax 56 0.032
466
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.032
467
c INT072 Intestinal Pseudo-Obstruction 56 0.032
468
NRL004 Neuroleptic Malignant Syndrome 56 0.032
469
PRP082 Porphyria, Congenital Erythropoietic 56 0.032
470
BRN004 Brain Edema 56 0.032
471
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.032
472
ATR057 Atrioventricular Block 55 0.032
473
NRN004 Neuroendocrine Tumor 55 0.032
474
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.032
475
P DYS193 Dystonia 11, Myoclonic 55 0.032
476
P MYP006 Myopia 55 0.032
477
END040 Endogenous Depression 55 0.032
478
RSC001 Rosacea 54 0.032
479
AMN001 Amenorrhea 54 0.032
480
HMS001 Hemosiderosis 54 0.032
481
PRS045 Prostatic Hypertrophy 53 0.032
482
GST009 Gastroschisis 53 0.032
483
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.032
484
NRT001 Neurotic Disorder 53 0.032
485
GST023 Gastric Ulcer 53 0.032
486
c FML008 Familial Retinoblastoma 53 0.032
487
c MCR113 Microvascular Complications of Diabetes 3 52 0.032
488
CHR073 Choreatic Disease 52 0.032
489
PRP016 Paraplegia 52 0.032
490
PTH003 Pathologic Nystagmus 52 0.032
491
HYP014 Hyperuricemia 52 0.032
492
NPH003 Nephrocalcinosis 51 0.032
493
THR004 Thrombocytosis 51 0.032
494
PRS021 Prostatic Adenoma 51 0.032
495
c ACT078 Acute Porphyria 51 0.032
496
INT071 Intestinal Perforation 51 0.032
497
BRX001 Bruxism 50 0.032
498
STM007 Stomatitis 50 0.032
499
c INF145 Infantile Liver Failure Syndrome 1 50 0.032
500
P TMP001 Temporal Lobe Epilepsy 50 0.032
501
PLC008 Placenta Disease 50 0.032
502
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.032
503
NTR046 Neutrophil Migration 50 0.032
504
P OBS001 Obstructive Jaundice 50 0.032
505
ISL003 Isolated Growth Hormone Deficiency 49 0.032
506
ADR038 Adermatoglyphia 49 0.032
507
AMB002 Amblyopia 49 0.032
508
PRS129 Prostatic Hyperplasia, Benign 49 0.032
509
URM002 Uremia 49 0.032
510
QDR001 Quadriplegia 48 0.032
511
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.032
512
LPT006 Leptin Receptor Deficiency 48 0.032
513
P PRP056 Porphyria, Acute Hepatic 48 0.032
514
SXL003 Sexual Disorder 47 0.032
515
c MLG069 Malignant Hypertension 47 0.032
516
CLF056 Cleft Lip with or Without Cleft Palate 47 0.032
517
RNL077 Renal Fibrosis 47 0.032
518
ACT084 Acute Stress Disorder 47 0.032
519
ANV001 Anovulation 47 0.032
520
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.032
521
LYM019 Lymphosarcoma 46 0.032
522
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.032
523
PLL012 Pollen Allergy 46 0.032
524
P MTH007 Methemoglobinemia 46 0.032
525
OBS003 Obsessive-Compulsive Personality Disorder 46 0.032
526
HDN002 Head Injury 46 0.032
527
c DRR009 Diarrhea 6 46 0.032
528
HPT004 Hepatic Coma 45 0.032
529
NWC001 Newcastle Disease 45 0.032
530
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.032
531
PRL008 Paralytic Ileus 45 0.032
532
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.032
533
ATN004 Autonomic Neuropathy 45 0.032
534
c CLR017 Clear Cell Sarcoma 45 0.032
535
P END039 Endodermal Sinus Tumor 44 0.032
536
KWS001 Kwashiorkor 44 0.032
537
P FBR003 Fibrous Histiocytoma 44 0.032
538
c ORT011 Orthostatic Hypotension 1 44 0.032
539
CRB090 Cerebral Hypoxia 44 0.032
540
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.032
541
DNT001 Dental Fluorosis 43 0.032
542
P HYP265 Hypotonia 43 0.032
543
P MJR007 Major Affective Disorder 1 43 0.032
544
GST020 Gastric Antral Vascular Ectasia 41 0.032
545
49X006 49, Xxxxy Syndrome 41 0.032
546
PRS063 Paresthesia 41 0.032
547
P RRH023 Rare Hereditary Hemochromatosis 41 0.032
548
VST004 Vestibular Disease 41 0.032
549
RDN001 Reading Disorder 40 0.032
550
P LTH003 Lethal Congenital Contracture Syndrome 40 0.032
551
ANG049 Angioedema Induced by Ace Inhibitors 40 0.032
552
LNG030 Lung Adenoma 39 0.032
553
SPP007 Suppression Amblyopia 39 0.032
554
TST018 Testicular Yolk Sac Tumor 39 0.032
555
c CHR682 Chronic Bilirubin Encephalopathy 39 0.032
556
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.032
557
ALX002 Alexithymia 38 0.032
558
HYP264 Hypertonia 38 0.032
559
CTN011 Cutaneous Porphyria 38 0.032
560
P FML187 Familial Hypertension 37 0.032
561
PRR004 Preretinal Fibrosis 37 0.032
562
GST004 Gastric Neuroendocrine Neoplasm 37 0.032
563
ABD010 Abdominal Wall Defect 36 0.032
564
PSD088 Pseudobulbar Affect 36 0.032
565
MTG002 Mutagen Sensitivity 35 0.032
566
CHR178 Chromosomal Triplication 35 0.032
567
PYR009 Pyridoxine Deficiency Anemia 34 0.032
568
c CHR064 Chronic Monocytic Leukemia 33 0.032
569
c PRS136 Prostate Cancer, Hereditary, 6 33 0.032
570
c PRS130 Prostate Cancer, Hereditary, 8 32 0.032
571
CRN270 Coronary Artery Dissection, Spontaneous 32 0.032
572
EXN003 Exencephaly 31 0.032
573
PLY150 Polykaryocytosis Inducer 31 0.032
574
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 0.032
575
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.032
576
c ORT012 Orthostatic Hypotension 2 26 0.032
577
BNG077 Benign Idiopathic Neonatal Seizures 26 0.032
578
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.032
579
ADG002 Audiogenic Seizures 25 0.032
580
c DMN005 Diamond-Blackfan Anemia 2 25 0.032
581
ANT078 Antipyrine Metabolism 24 0.032
582
INF043 Infantile Apnea 22 0.032
583
HYP188 Hypnic Headache 20 0.032
585
OBN001 Ouabain Resistance 18 0.032
586
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 14 0.032
587
ESP021 Esophageal Cancer 90 0.022
588
P RTT002 Rett Syndrome 80 0.022
589
c NRF023 Neurofibromatosis, Type Ii 80 0.022
590
INS024 Insulin-Like Growth Factor I 79 0.022
591
P LYN001 Lynch Syndrome 77 0.022
592
P MDL005 Medulloblastoma 77 0.022
593
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.022
594
c NRF024 Neurofibromatosis, Type I 77 0.022
595
P NJM001 Nijmegen Breakage Syndrome 74 0.022
596
c THR092 Thrombophilia Due to Thrombin Defect 73 0.022
597
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.022
598
c LKM063 Leukemia, Chronic Myeloid 72 0.022
599
P ATS364 Autism 70 0.022
600
GST040 Gastric Adenocarcinoma 70 0.022
601
MLT157 Multiple System Atrophy 1 70 0.022
602
P TTR001 Tetralogy of Fallot 70 0.022
603
WRN001 Werner Syndrome 69 0.022
604
PLY001 Polycythemia Vera 69 0.022
605
PLM001 Pulmonary Tuberculosis 69 0.022
606
LYM133 Lymphoma, Hodgkin, Classic 69 0.022
607
P OCL013 Oculodentodigital Dysplasia 69 0.022
608
P HYP086 Hypothyroidism 69 0.022
609
P MPL001 Maple Syrup Urine Disease 69 0.022
610
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.022
611
P LYM118 Lymphoma 68 0.022
612
P CRN037 Craniosynostosis 68 0.022
613
P PNM007 Pneumonia 68 0.022
614
P MYC084 Mycobacterium Tuberculosis 1 68 0.022
615
P MYS003 Myasthenia Gravis 68 0.022
616
P INF038 Influenza 68 0.022
617
RCK004 Rickets 68 0.022
618
HYL004 Hyaline Fibromatosis Syndrome 67 0.022
619
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.022
620
BLM001 Bloom Syndrome 67 0.022
621
c ATS007 Autism Spectrum Disorder 67 0.022
622
CRP001 Carpal Tunnel Syndrome 67 0.022
623
P CLC063 Celiac Disease 1 66 0.022
624
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.022
625
ANG054 Angina Pectoris 66 0.022
626
P MCR115 Microvascular Complications of Diabetes 5 66 0.022
627
c MCR129 Microvascular Complications of Diabetes 1 66 0.022
628
P MNN013 Meningitis 66 0.022
629
P CCK001 Cockayne Syndrome 66 0.022
630
MYL031 Myeloproliferative Neoplasm 66 0.022
631
KHL003 Kohlschutter-Tonz Syndrome 65 0.022
632
P PLM036 Pulmonary Fibrosis 65 0.022
633
P ART005 Arteriovenous Malformation 65 0.022
634
KRT019 Keratitis, Hereditary 65 0.022
635
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.022
636
P LPS002 Liposarcoma 65 0.022
637
IRR002 Irritable Bowel Syndrome 65 0.022
638
CHY002 Chylomicron Retention Disease 65 0.022
639
c WLM013 Wilms Tumor 1 65 0.022
640
CLN015 Colon Adenocarcinoma 65 0.022
641
P THY023 Thymoma 65 0.022
642
PRT036 Peritonitis 64 0.022
643
NRF007 Neurofibroma 64 0.022
644
PLM031 Poliomyelitis 64 0.022
645
c EPS035 Episodic Ataxia, Type 2 63 0.022
646
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.022
647
P NTR004 Neutropenia 63 0.022
648
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.022
649
SKN016 Skin Disease 63 0.022
650
P HYP055 Hypoplastic Left Heart Syndrome 63 0.022
651
HMT002 Hematologic Cancer 62 0.022
652
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.022
653
c SVR001 Severe Acute Respiratory Syndrome 62 0.022
654
P HYP750 Hypertriglyceridemia, Familial 62 0.022
655
P ART023 Arthropathy 62 0.022
656
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.022
657
CRC021 Carcinosarcoma 62 0.022
658
BLD131 Bladder Urothelial Carcinoma 62 0.022
659
ESP020 Esophageal Atresia 62 0.022
660
P INT143 Interstitial Cystitis 61 0.022
661
P ENC004 Encephalitis 61 0.022
662
c WLM018 Wilms Tumor 5 61 0.022
663
P PNC044 Pancreatitis 61 0.022
664
VRL011 Viral Infectious Disease 61 0.022
665
P LPS004 Lupus Erythematosus 61 0.022
666
DCB001 Decubitus Ulcer 61 0.022
667
NRL005 Neurilemmoma 60 0.022
668
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.022
669
TRG002 Trigeminal Neuralgia 60 0.022
670
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.022
671
INT066 Interstitial Lung Disease 60 0.022
672
c ACT027 Acute Pancreatitis 60 0.022
673
c LYN004 Lynch Syndrome I 60 0.022
674
P ATR010 Atrial Heart Septal Defect 60 0.022
675
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.022
676
P SNS001 Sensorineural Hearing Loss 60 0.022
677
ORL011 Oral Cancer 60 0.022
678
INS001 Insulinoma 60 0.022
679
P EPS003 Episodic Ataxia 59 0.022
680
P MYC008 Myocarditis 59 0.022
681
P MCR010 Microcephaly 59 0.022
682
CHL014 Cholera 59 0.022
683
IDP011 Idiopathic Interstitial Pneumonia 59 0.022
684
c HPT016 Hepatitis B 59 0.022
685
c DNG003 Dengue Disease 59 0.022
686
PLM033 Pulmonary Embolism 59 0.022
687
AVN001 Avian Influenza 59 0.022
688
GNG013 Gingivitis 59 0.022
689
IRN001 Iron Deficiency Anemia 59 0.022
690
P DNG005 Dengue Virus 59 0.022
691
VLV032 Vulva Cancer 59 0.022
692
INC002 Inclusion Body Myositis 58 0.022
693
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.022
694
GLB001 Gilbert Syndrome 58 0.022
695
P PLV020 Pelvic Organ Prolapse 57 0.022
696
DSS009 Disseminated Intravascular Coagulation 57 0.022
697
P PRN023 Prion Disease 57 0.022
698
THR024 Thrombosis 57 0.022
699
APH002 Aphasia 57 0.022
700
P FTL001 Fetal Alcohol Syndrome 57 0.022
701
HMR039 Hemorrhage, Intracerebral 57 0.022
702
JPN002 Japanese Encephalitis 57 0.022
703
PHR003 Pharyngitis 57 0.022
704
P MYS005 Myositis 56 0.022
705
P PLY018 Polycythemia 56 0.022
706
P CHN012 Chondrosarcoma 56 0.022
707
CMR002 Coumarin Resistance 56 0.022
708
P PLY011 Polycystic Ovary Syndrome 56 0.022
709
TRN018 Transitional Cell Carcinoma 56 0.022
710
PLS011 Plasmacytoma 56 0.022
711
ERY051 Erythroleukemia, Familial 56 0.022
712
P NRP001 Neuropathy 56 0.022
713
BCT022 Bacterial Infectious Disease 56 0.022
714
SCH003 Schizophreniform Disorder 56 0.022
715
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.022
716
ANN002 Anencephaly 56 0.022
717
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.022
718
P NRF002 Neurofibromatosis 56 0.022
719
EMB004 Embryonal Carcinoma 56 0.022
720
GST050 Gastrointestinal System Disease 56 0.022
721
c GRV008 Graves Disease 1 56 0.022
722
P MYT023 Myotonia Congenita 56 0.022
723
P AGN002 Agnosia 55 0.022
724
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.022
725
MCL006 Macular Retinal Edema 55 0.022
726
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.022
727
LMB062 Limb Ischemia 55 0.022
728
P MLN007 Male Infertility 55 0.022
729
DFF005 Diffuse Large B-Cell Lymphoma 55 0.022
730
P PLM034 Pulmonary Emphysema 55 0.022
731
P PTT006 Pituitary Adenoma 55 0.022
732
P HYP076 Hyperthyroidism 55 0.022
733
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.022
734
CLF004 Cleft Lip/palate 54 0.022
735
TRD006 Tardive Dyskinesia 54 0.022
736
MNN032 Meningococcal Meningitis 54 0.022
737
VGN023 Vaginitis 54 0.022
738
P NLD001 Nail Disease 54 0.022
739
P CYS039 Cystic Kidney Disease 54 0.022
740
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.022
741
P INF037 Inflammatory Bowel Disease 54 0.022
742
MYM001 Myoma 54 0.022
743
P FML012 Familial Partial Lipodystrophy 54 0.022
744
P TCD001 Tic Disorder 53 0.022
745
HRT012 Heart Valve Disease 53 0.022
746
P FML023 Familial Hemiplegic Migraine 53 0.022
747
BRN038 Bronchial Disease 53 0.022
748
P PTS002 Ptosis 53 0.022
749
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.022
750
HMC014 Homocysteinemia 53 0.022
751
P FBR031 Febrile Seizures 53 0.022
752
PRP080 Peripheral Artery Disease 53 0.022
753
P INT068 Intestinal Disease 53 0.022
754
P RTN018 Retinal Disease 53 0.022
755
PLS007 Plasmodium Falciparum Malaria 52 0.022
756
P PRR016 Pierre Robin Syndrome 52 0.022
757
c THY107 Thymoma, Familial 52 0.022
758
ART074 Aortic Dissection 52 0.022
759
DSM007 Desmoplastic Small Round Cell Tumor 52 0.022
760
OLG003 Oligohydramnios 51 0.022
761
P SPP010 Suppressor of Tumorigenicity 3 51 0.022
762
FDL002 Food Allergy 51 0.022
763
CND002 Conduct Disorder 51 0.022
764
MYL001 Myelitis 51 0.022
765
ANK001 Ankylosis 51 0.022
766
c PNC106 Pancreatic Agenesis 1 51 0.022
767
P HYP040 Hypospadias 51 0.022
768
P CHL066 Cholangitis 51 0.022
769
CHR005 Chorioamnionitis 51 0.022
770
PRT029 Parathyroid Adenoma 50 0.022
771
PLR008 Pleurisy 50 0.022
772
c HNT004 Huntington Disease-Like 2 50 0.022
773
RTN003 Retinal Ischemia 50 0.022
774
HPT014 Hepatorenal Syndrome 50 0.022
775
CRN030 Coronary Stenosis 50 0.022
776
c XRD032 Xeroderma Pigmentosum, Complementation Group B 50 0.022
777
CLR003 Clear Cell Adenocarcinoma 50 0.022
778
P OMP004 Omphalocele 50 0.022
779
HYP017 Hypophosphatemia 50 0.022
780
c DYS119 Dystonia 9 50 0.022
781
P MYT002 Myotonic Dystrophy 49 0.022
782
SYS003 Systolic Heart Failure 49 0.022
783
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.022
784
BKR002 Baker-Gordon Syndrome 49 0.022
785
CHL004 Cholelithiasis 49 0.022
786
ACT029 Acute Interstitial Pneumonia 49 0.022
787
P BRS053 Breast Fibroadenoma 49 0.022
788
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.022
789
HPT009 Hepatopulmonary Syndrome 48 0.022
790
DBT006 Diabetic Macular Edema 48 0.022
791
PNC034 Pancreas Disease 48 0.022
792
SPL018 Splenomegaly 48 0.022
793
c CRN241 Corneal Dystrophy, Congenital Stromal 48 0.022
794
RCT020 Rectum Adenocarcinoma 48 0.022
795
HRN026 Hernia, Hiatus 47 0.022
796
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.022
797
PRD004 Prediabetes Syndrome 47 0.022
798
ACT055 Actinomycosis 47 0.022
799
c MCR120 Microvascular Complications of Diabetes 7 47 0.022
800
KRT002 Keratomalacia 47 0.022
801
P ENC008 Encephalocele 47 0.022
802
SRT004 Serotonin Syndrome 47 0.022
803
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.022
804
P CRC039 Coarctation of Aorta 47 0.022
805
NDL013 Nodular Regenerative Hyperplasia 47 0.022
806
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.022
807
HYP034 Hypertensive Encephalopathy 46 0.022
808
MTS001 Mutism 46 0.022
809
CLN045 Colonic Benign Neoplasm 46 0.022
810
KRT013 Keratolytic Winter Erythema 46 0.022
811
UMB002 Umbilical Hernia 46 0.022
812
P BNG032 Benign Mesothelioma 46 0.022
813
c SCH079 Schizophrenia 1 46 0.022
814
c MLG068 Malignant Glioma 46 0.022
815
BNS007 Bone Sarcoma 45 0.022
816
OLG001 Oligospermia 45 0.022
817
RTR008 Root Resorption 45 0.022
818
GLC022 Glucose/galactose Malabsorption 45 0.022
819
TRT001 Teratocarcinoma 45 0.022
820
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.022
821
CRB004 Cerebral Artery Occlusion 45 0.022
822
CRT015 Carotid Artery Occlusion 45 0.022
823
SPS057 Spasticity 45 0.022
824
RTR001 Retrograde Amnesia 44 0.022
825
P EPT012 Epithelioid Sarcoma 44 0.022
826
c CHR579 Chiari Malformation Type Ii 44 0.022
827
IMM064 Immunodeficiency, Common Variable, 10 44 0.022
828
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.022
829
c FBR070 Febrile Seizures, Familial, 8 44 0.022
830
PRM003 Premature Ejaculation 44 0.022
831
c HYP272 Hypercholesterolemia, Familial, 3 44 0.022
832
DMP001 Dumping Syndrome 44 0.022
833
c SPR086 Spermatogenic Failure 3 44 0.022
834
CVD001 Covid-19 44 0.022
835
DPR002 Depersonalization Disorder 43 0.022
836
RFR003 Refractive Error 43 0.022
837
PLY068 Polysubstance Abuse 43 0.022
838
MDD018 Middle East Respiratory Syndrome 43 0.022
839
DRG002 Drug-Induced Hepatitis 43 0.022
840
MCR103 Microtia 43 0.022
841
P CLS010 Cluster Headache 42 0.022
842
TRP014 Triploidy 42 0.022
843
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.022
844
CRB025 Carbohydrate Metabolic Disorder 41 0.022
845
P CHR342 Chiari Malformation 41 0.022
846
P HYP263 Hypersomnia 41 0.022
847
c MCR130 Microvascular Complications of Diabetes 6 41 0.022
848
c MCR133 Microvascular Complications of Diabetes 4 41 0.022
849
MMM006 Mammographic Density 41 0.022
850
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 41 0.022
851
ACT088 Acute Insulin Response 41 0.022
852
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.022
853
FNC002 Functional Diarrhea 41 0.022
854
P RRT020 Rare Tumor 41 0.022
855
ISL151 Isolated Elevated Serum Creatine Phosphokinase Levels 40 0.022
856
PLM030 Pleomorphic Rhabdomyosarcoma 40 0.022
857
P MLG074 Malignant Mesenchymoma 40 0.022
858
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.022
859
INT060 Intestinal Atresia 40 0.022
860
SPR126 Superior Semicircular Canal Dehiscence 40 0.022
861
GLC008 Glucose Metabolism Disease 40 0.022
862
HYP540 Hypertension, Diastolic 40 0.022
863
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.022
864
ADJ001 Adjustment Disorder 40 0.022
865
CRD005 Cardia Cancer 40 0.022
866
CNN001 Cannabis Dependence 40 0.022
867
P TRC031 Trichorhinophalangeal Syndrome 40 0.022
868
MLT001 Multiple Chemical Sensitivity 40 0.022
869
OCL010 Ocular Hypotension 39 0.022
870
EXT006 Extrahepatic Cholestasis 39 0.022
871
c HMG029 Hemoglobin Se Disease 39 0.022
872
SCR011 Scrapie 39 0.022
873
HYP835 Hypothalamic Obesity 38 0.022
874
PST029 Postmenopausal Atrophic Vaginitis 38 0.022
875
c HNT011 Huntington Disease-Like 3 38 0.022
876
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.022
877
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.022
878
AMP007 Amphetamine Abuse 37 0.022
879
c BLP048 Blepharospasm, Benign Essential 37 0.022
880
HRN029 Hearing Loss, Noise-Induced 37 0.022
881
P FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 37 0.022
882
HYP026 Hypoglycemic Coma 36 0.022
883
CRD245 Cardiac-Urogenital Syndrome 36 0.022
884
WHP002 Whiplash 36 0.022
886
DNT008 Denture Stomatitis 35 0.022
887
c MCR312 Microphthalmia, Syndromic 10 35 0.022
888
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.022
889
DSN001 De Sanctis-Cacchione Syndrome 35 0.022
890
TTH004 Tethered Spinal Cord Syndrome 35 0.022
891
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.022
892
c MJR008 Major Affective Disorder 2 35 0.022
893
MYT011 Myotonia 34 0.022
894
P EXT032 Extraosseous Osteosarcoma 34 0.022
895
c RST012 Restless Legs Syndrome 1 34 0.022
896
c CLR066 Ciliary Dyskinesia, Primary, 2 34 0.022
897
PLM028 Pulmonary Coin Lesion 33 0.022
898
c MJR023 Major Affective Disorder 7 33 0.022
899
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.022
900
c MJR003 Major Affective Disorder 6 33 0.022
901
c MJR006 Major Affective Disorder 5 33 0.022
902
c PRG003 Progesterone-Receptor Negative Breast Cancer 33 0.022
903
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.022
904
HND015 Hand Skill, Relative 33 0.022
905
NSL006 Nasal Cavity Squamous Cell Carcinoma 33 0.022
906
MTB016 Metabolic Myopathy 32 0.022
907
c LCL022 Localized Lipodystrophy 32 0.022
908
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.022
909
SPR017 Spermatocele 31 0.022
910
GST007 Gastric Dilatation 31 0.022
911
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 31 0.022
912
FCT008 Factitious Disorder 31 0.022
913
GRN004 Granulomatous Amebic Encephalitis 30 0.022
914
LMB010 Lambert Syndrome 30 0.022
915
PRT006 Partial Motor Epilepsy 29 0.022
916
PST092 Posttransplant Acute Limbic Encephalitis 29 0.022
917
c MJR004 Major Affective Disorder 4 28 0.022
918
c MLG151 Malignant Hyperthermia 5 28 0.022
919
c TRC073 Treacher Collins Syndrome 2 27 0.022
920
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.022
921
ENM002 Enamel Erosion 26 0.022
922
IMM002 Immature Cataract 25 0.022
923
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.022
924
CLN012 Colon Leiomyosarcoma 25 0.022
925
DSS025 Dissociative Seizures 25 0.022
926
NN2002 Non 24 Hour Sleep Wake Disorder 24 0.022
927
SML003 Small Cell Osteogenic Sarcoma 24 0.022
928
PRX022 Paroxysmal Choreoathetosis 24 0.022
929
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.022
930
P SLF001 Sulfhemoglobinemia 23 0.022
931
SDD004 Sudden Arrhythmia Death Syndrome 22 0.022
932
c PRX024 Paroxysmal Nonkinesigenic Dyskinesia 2 21 0.022
933
c MYP040 Myopia 7 20 0.022
934
c SLV029 Silver-Russell Syndrome 2 19 0.022
935
BDR001 Bidirectional Tachycardia 19 0.022
936
STN005 St Anthony's Fire 17 0.022
937
FRC013 Fructose Utilization 15 0.022
938
DGT004 Digitalis Poisoning 14 0.022
939
NRL025 Neural Tube Closure Defect 12 0.022
940
PRX087 Paroxysomal Nonkinesigenic Dyskinesia 2 0.022
Content
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