Search results for Caffeine

913 hits were found for Caffeine

# Family MCID Name MIFTS Score
1
APN006 Apnea of Prematurity 24 0.281
2
P HDC001 Headache 58 0.272
3
c MGR028 Migraine with or Without Aura 1 70 0.234
4
P MLG056 Malignant Hyperthermia 68 0.220
5
BRN056 Bronchopulmonary Dysplasia 58 0.196
6
P LVR013 Liver Disease 68 0.178
7
ANX010 Anxiety 73 0.173
8
P TRM003 Tremor 54 0.169
9
P SZR006 Seizure Disorder 59 0.167
10
48X005 48,xyyy 39 0.164
11
CYT018 Cytochrome P450 2d6 Variant 27 0.164
12
VSL002 Visual Epilepsy 57 0.161
13
c EPS039 Episodic Pain Syndrome, Familial, 1 41 0.157
14
c PNS012 Paine Syndrome 61 0.145
15
HYP266 Hypoxia 57 0.142
16
WTH001 Withdrawal Disorder 49 0.142
17
LVR012 Liver Cirrhosis 64 0.140
18
PNG002 Pain Agnosia 51 0.134
19
P PRK057 Parkinson Disease, Late-Onset 77 0.130
20
ISC004 Ischemia 61 0.130
21
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.130
22
P PNC025 Panic Disorder 53 0.128
23
OST159 Osteogenic Sarcoma 67 0.126
24
P ATX030 Ataxia-Telangiectasia 84 0.122
25
PSY004 Psychotic Disorder 67 0.122
26
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.122
27
TLN003 Telangiectasis 52 0.122
28
P PTN014 Patent Ductus Arteriosus 1 60 0.117
29
CRB037 Cerebral Palsy 68 0.115
30
P SKN015 Skin Carcinoma 67 0.115
31
P BDY004 Body Mass Index Quantitative Trait Locus 11 77 0.113
32
XRD010 Xeroderma Pigmentosum, Variant Type 74 0.113
33
c BDY021 Body Mass Index Quantitative Trait Locus 20 53 0.113
34
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.113
35
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.113
36
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.113
37
c BDY010 Body Mass Index Quantitative Trait Locus 4 47 0.113
38
c BDY015 Body Mass Index Quantitative Trait Locus 12 47 0.113
39
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.113
40
c BDY011 Body Mass Index Quantitative Trait Locus 10 46 0.113
41
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.113
42
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.113
43
BRS051 Breast Disease 58 0.110
44
P ATR011 Atrial Fibrillation 66 0.108
45
HYP056 Hypoglycemia 66 0.108
46
DPR016 Depression 64 0.108
47
P ALZ034 Alzheimer Disease 89 0.105
48
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.105
49
P CRN300 Coronary Heart Disease 1 64 0.105
50
FTT001 Fatty Liver Disease 62 0.105
51
P SLP005 Sleep Disorder 60 0.105
52
SBS004 Substance Dependence 48 0.105
53
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.105
54
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.100
55
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.097
56
P SLP006 Sleep Apnea 69 0.097
57
P CRN018 Coronary Artery Anomaly 64 0.097
58
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.097
59
DWN001 Down Syndrome 71 0.095
60
c EXD008 Exudative Vitreoretinopathy 1 70 0.095
61
ART140 Arteries, Anomalies of 53 0.095
62
BRN071 Brain Injury 50 0.095
63
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.095
64
P NRB001 Neuroblastoma 72 0.092
65
P SBS003 Substance Abuse 55 0.092
66
ENT011 Enterocolitis 51 0.092
67
ATX019 Ataxia with Vitamin E Deficiency 48 0.092
68
P CLR023 Colorectal Cancer 99 0.089
69
LNG099 Lung Disease 61 0.089
70
P CTR002 Cataract 61 0.089
71
HYP005 Hypokalemia 56 0.089
72
P OVR042 Ovarian Cancer 90 0.086
73
P HRT032 Heart Disease 76 0.086
74
P CRD119 Cardiac Arrest 68 0.086
75
ALC007 Alcohol Dependence 67 0.086
76
ATH013 Atherosclerosis Susceptibility 66 0.086
77
CLF027 Cleft Palate, Isolated 65 0.086
78
HYP066 Hyperglycemia 61 0.086
79
MNT002 Mental Depression 57 0.086
80
MLG086 Malignant Hyperthermia Susceptibility 41 0.086
81
RPD005 Rapidly Involuting Congenital Hemangioma 39 0.086
82
P HPT023 Hepatocellular Carcinoma 100 0.083
83
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.083
84
P ENC018 Encephalopathy 61 0.083
85
PRN019 Perinatal Necrotizing Enterocolitis 55 0.083
86
ADL002 Adult Syndrome 70 0.080
87
P MJR001 Major Depressive Disorder 68 0.080
88
P TRN020 Turner Syndrome 65 0.080
89
APN008 Apnea, Obstructive Sleep 65 0.080
90
P DBT009 Diabetes Mellitus 65 0.080
91
ALL026 Allergic Hypersensitivity Disease 64 0.080
92
c HPT001 Hepatitis C 63 0.080
93
CCN002 Cocaine Abuse 48 0.080
94
BCK006 Back Pain 42 0.080
95
AST005 Asthma 77 0.076
96
P SCH015 Schizophrenia 75 0.076
97
P RSP003 Respiratory Failure 75 0.076
98
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.076
99
LPT014 Leptin Deficiency or Dysfunction 74 0.076
100
P OST002 Osteoporosis 74 0.076
101
CRB039 Cerebrovascular Disease 69 0.076
102
SRC014 Sarcoma 66 0.076
103
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.076
104
NTR005 Nutritional Deficiency Disease 62 0.076
105
BRN002 Bronchiolitis 59 0.076
106
P ALC033 Alcohol Use Disorder 59 0.076
107
TRM010 Traumatic Brain Injury 53 0.076
108
SPN035 Spindle Cell Sarcoma 51 0.076
109
P DDN001 Duodenal Ulcer 50 0.076
110
47X002 47,xyy 49 0.076
111
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.076
112
SBC016 Subacute Delirium 44 0.076
113
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.076
114
RST023 Resting Heart Rate, Variation in 42 0.076
115
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.076
116
CHL079 Children's Interstitial Lung Disease 27 0.076
117
P HNT016 Huntington Disease 72 0.073
118
P MYC007 Myocardial Infarction 71 0.073
119
P KDN018 Kidney Disease 71 0.073
120
P DMN002 Dementia 68 0.073
121
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.073
122
PPL049 Papillon-Lefevre Syndrome 63 0.073
123
P BLD124 Bleeding Disorder, Platelet-Type, 11 62 0.073
124
P MVM001 Movement Disease 62 0.073
125
P CRD246 Cardiovascular System Disease 56 0.073
126
ILS001 Ileus 51 0.073
127
SPS003 Spastic Diplegia 51 0.073
128
CYT002 Cytokine Deficiency 44 0.073
129
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.069
130
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.069
131
P PNC035 Pancreatic Cancer 85 0.069
132
c HYP595 Hypertension, Essential 85 0.069
133
GLB015 Glioblastoma Multiforme 75 0.069
134
P DRM053 Dermatitis, Atopic 67 0.069
135
P MYP004 Myopathy 65 0.069
136
TBC004 Tobacco Addiction 64 0.069
137
TTN003 Tetanus 64 0.069
138
P ADN016 Adenocarcinoma 64 0.069
139
c PRC016 Pre-Eclampsia 64 0.069
140
P GLM045 Glioma 63 0.069
141
P PSR002 Psoriasis 63 0.069
142
CRD223 Cardiac Arrhythmia 61 0.069
143
c ACT071 Acute Kidney Failure 60 0.069
144
P INF032 Infertility 58 0.069
145
P LTR001 Lateral Sclerosis 54 0.069
146
OCL006 Ocular Hypertension 54 0.069
147
PST011 Pustulosis of Palm and Sole 53 0.069
148
MCN017 Meconium Ileus 52 0.069
149
OCL069 Ocular Motor Apraxia 52 0.069
150
P CHR345 Chronic Pain 50 0.069
151
VTM033 Vitamin K Deficiency Bleeding 49 0.069
152
DRG003 Drug Dependence 48 0.069
153
GLL048 Glial Tumor 46 0.069
154
P BRS047 Breast Cancer 97 0.065
155
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.065
156
P HPT021 Hepatitis 68 0.065
157
P HRP006 Herpes Simplex 65 0.065
158
SPN186 Spinal Cord Injury 61 0.065
159
ADN018 Adenoma 59 0.065
160
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.065
161
SFT003 Soft Tissue Sarcoma 57 0.065
162
P ALP008 Alopecia 56 0.065
163
AMN003 Amnestic Disorder 55 0.065
164
HYP060 Hyperinsulinism 55 0.065
165
GLC003 Glucose Intolerance 54 0.065
166
P OPN001 Open-Angle Glaucoma 49 0.065
167
TTH006 Tooth Disease 47 0.065
168
CYN002 Cyanosis, Transient Neonatal 46 0.065
169
LWC001 Low Compliance Bladder 43 0.065
170
HRW001 Hair Whorl 36 0.065
171
STR067 Stroke, Ischemic 80 0.061
172
END057 Endometrial Cancer 75 0.061
173
P CNR004 Cone-Rod Dystrophy 2 72 0.061
174
CNG034 Congestive Heart Failure 70 0.061
175
MLN008 Melanoma 69 0.061
176
c RHB024 Rhabdomyosarcoma 2 66 0.061
177
P VSC007 Vascular Disease 64 0.061
178
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.061
179
c GLC092 Glaucoma, Primary Open Angle 62 0.061
180
MDD011 Mood Disorder 62 0.061
181
DRM006 Dermatitis 62 0.061
182
SDD001 Sudden Infant Death Syndrome 61 0.061
183
ETN001 Eating Disorder 60 0.061
184
c ACT075 Acute Myocardial Infarction 57 0.061
185
PRV004 Periventricular Leukomalacia 52 0.061
186
P NRC002 Narcolepsy 52 0.061
187
NNL006 Non-Alcoholic Steatohepatitis 51 0.061
188
SCH012 Schizoaffective Disorder 51 0.061
189
MTB004 Metabolic Acidosis 50 0.061
190
P RNV001 Renovascular Hypertension 49 0.061
191
CCN001 Cocaine Dependence 49 0.061
192
c SPL067 Split-Hand/foot Malformation 1 48 0.061
193
ISL121 Isolated Split Hand-Split Foot Malformation 47 0.061
194
AND014 Androgenic Alopecia 45 0.061
195
OVR094 Ovarian Epithelial Cancer 38 0.061
196
PPL052 Papillomatosis, Confluent and Reticulated 34 0.061
197
NRL016 Neural Tube Defects 83 0.056
198
CYS001 Cystic Fibrosis 80 0.056
199
c HYP836 Hypercholesterolemia, Familial, 1 73 0.056
200
PNC129 Pancreatic Adenocarcinoma 68 0.056
201
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 67 0.056
202
P MSC005 Muscular Dystrophy 66 0.056
203
GST092 Gastroesophageal Reflux 65 0.056
204
GT001 Gout 64 0.056
205
ANR007 Anorexia Nervosa 63 0.056
206
c HPT003 Hepatitis a 63 0.056
207
CRD132 Cardiac Conduction Defect 59 0.056
208
NWB001 Newborn Respiratory Distress Syndrome 58 0.056
209
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.056
210
P DRR001 Diarrhea 56 0.056
211
MYP139 Myopathy, Proximal, and Ophthalmoplegia 54 0.056
212
P ECL001 Eclampsia 51 0.056
213
P ALP061 Alopecia, Androgenetic, 1 50 0.056
214
LRN003 Learning Disability 49 0.056
215
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.056
216
P SMK004 Smoking As a Quantitative Trait Locus 3 45 0.056
217
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.056
218
PRM020 Premenstrual Tension 39 0.056
219
P LNG032 Lung Cancer 98 0.051
220
P PRS040 Prostate Cancer 98 0.051
221
P BLD134 Bladder Cancer 79 0.051
222
P LNG064 Lung Cancer Susceptibility 3 78 0.051
223
DFC004 Deficiency Anemia 75 0.051
224
SCK003 Sickle Cell Anemia 73 0.051
225
MSC157 Muscular Dystrophy, Duchenne Type 72 0.051
226
P PHC003 Pheochromocytoma 72 0.051
227
PRP027 Peripheral Vascular Disease 72 0.051
228
c HPT073 Hepatitis C Virus 71 0.051
229
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.051
230
P ART022 Arthritis 71 0.051
231
OBS002 Obsessive-Compulsive Disorder 69 0.051
232
BRN024 Bronchitis 69 0.051
233
c FML001 Familial Atrial Fibrillation 67 0.051
234
P NRV007 Nervous System Disease 66 0.051
235
PRT037 Pertussis 66 0.051
236
c FNC043 Fanconi Anemia, Complementation Group E 63 0.051
237
INT002 Intermittent Claudication 62 0.051
238
c BRN108 Branchiootic Syndrome 1 61 0.051
239
P END044 Endometriosis 61 0.051
240
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.051
241
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.051
242
PRT058 Pure Autonomic Failure 60 0.051
243
P PLY014 Polycystic Kidney Disease 60 0.051
244
PPT005 Peptic Ulcer Disease 59 0.051
245
c ESS001 Essential Tremor 57 0.051
246
P FBR017 Fibrosarcoma 57 0.051
247
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.051
248
GNR004 Generalized Anxiety Disorder 56 0.051
249
CMM005 Common Cold 56 0.051
250
P GST044 Gastritis 56 0.051
251
PPL022 Papilloma 55 0.051
252
IMP005 Impotence 52 0.051
253
MTN003 Motion Sickness 52 0.051
254
P SCK005 Sickle Cell Disease 51 0.051
255
c SPN330 Spondylocostal Dysostosis 5 49 0.051
256
P MGR001 Migraine Without Aura 48 0.051
257
c HYD064 Hydrocephalus, Congenital, 1 47 0.051
258
ADR040 Adrenal Gland Pheochromocytoma 46 0.051
259
AGR002 Agoraphobia 45 0.051
260
c PRM038 Primary Agammaglobulinemia 44 0.051
261
TRP009 Triple X Syndrome 43 0.051
262
c MLG147 Malignant Hyperthermia 1 43 0.051
263
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.051
264
ENT001 Enterocele 39 0.051
265
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.051
266
ACT240 Actn3 Deficiency 24 0.051
267
ACT133 Acetylation, Slow 23 0.051
268
P GST053 Gastric Cancer 84 0.046
269
P RHM011 Rheumatoid Arthritis 81 0.046
270
HMN044 Human Immunodeficiency Virus Type 1 71 0.046
271
c BSL007 Basal Cell Carcinoma 69 0.046
272
SKN019 Skin Melanoma 68 0.046
273
ALL003 Allergic Rhinitis 68 0.046
274
UND005 Undifferentiated Pleomorphic Sarcoma 67 0.046
275
P HYD006 Hydrocephalus 66 0.046
276
c DPH024 Diaphragmatic Hernia, Congenital 65 0.046
277
MSC007 Muscle Hypertrophy 64 0.046
278
P ADL010 Adult Respiratory Distress Syndrome 63 0.046
279
LPD008 Lipid Metabolism Disorder 63 0.046
280
LSC001 Lesch-Nyhan Syndrome 63 0.046
281
PSR001 Psoriatic Arthritis 62 0.046
282
HYD038 Hydrops Fetalis, Nonimmune 62 0.046
283
P PRM006 Primary Biliary Cirrhosis 62 0.046
284
P URT039 Urticaria 58 0.046
285
END030 End Stage Renal Failure 58 0.046
286
CNS004 Constipation 58 0.046
287
BLM002 Bulimia Nervosa 58 0.046
288
BLR008 Bilirubin Metabolic Disorder 58 0.046
289
DSS008 Disease of Mental Health 57 0.046
290
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.046
291
P BPL003 Bipolar Disorder 57 0.046
292
c FML035 Familial Hyperlipidemia 56 0.046
293
PLM010 Pulmonary Edema 55 0.046
294
PRT038 Protein-Energy Malnutrition 55 0.046
295
P RST001 Restless Legs Syndrome 55 0.046
296
c CNT035 Central Nervous System Disease 54 0.046
297
ALC009 Alcoholic Liver Cirrhosis 54 0.046
298
CLF001 Cleft Lip 53 0.046
299
c GLL024 Gallbladder Disease 1 52 0.046
300
P MGR003 Migraine with Aura 50 0.046
301
c CNG216 Congenital Hydrocephalus 50 0.046
302
OPT003 Opiate Dependence 50 0.046
303
c PSR017 Psoriasis 2 50 0.046
304
c PSR023 Psoriasis 1 49 0.046
305
BNR002 Bone Resorption Disease 49 0.046
306
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.046
307
PLC007 Placental Abruption 48 0.046
308
OPD006 Opioid Addiction 48 0.046
309
HLX001 Helix Syndrome 48 0.046
310
c LRG017 Large Intestine Cancer 47 0.046
311
c INH020 Inherited Metabolic Disorder 46 0.046
312
OPD001 Opioid Abuse 46 0.046
313
TRC097 Tracheomalacia 45 0.046
314
DVR002 Diverticulitis 44 0.046
315
CNT017 Central Nervous System Origin Vertigo 44 0.046
316
P PRC031 Preeclampsia/eclampsia 1 44 0.046
317
BSL008 Basal Ganglia Disease 43 0.046
318
SQM002 Squamous Cell Papilloma 43 0.046
319
ANX004 Anoxia 42 0.046
320
c MJR024 Major Affective Disorder 9 41 0.046
321
c PSR028 Psoriasis 7 39 0.046
322
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 39 0.046
323
c PSR032 Psoriasis 11 39 0.046
324
c PSR018 Psoriasis 13 39 0.046
325
c MJR022 Major Affective Disorder 8 38 0.046
326
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.046
327
DVL001 Developmental Coordination Disorder 35 0.046
328
EMP011 Emphysema, Congenital Lobar 34 0.046
329
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.046
330
RSP007 Respiratory Distress Syndrome, Infant 30 0.046
331
DVL005 Developmental Dyspraxia 23 0.046
332
c FNC027 Fanconi Anemia, Complementation Group a 82 0.040
333
MLR004 Malaria 81 0.040
334
OST012 Osteoarthritis 78 0.040
335
GST019 Gastrointestinal Stromal Tumor 77 0.040
336
CRH001 Crohn's Disease 75 0.040
337
c ATR087 Atrial Standstill 1 74 0.040
338
SVR004 Severe Combined Immunodeficiency 74 0.040
339
c SPN225 Spondyloarthropathy 1 74 0.040
340
P MLT020 Multiple Sclerosis 72 0.040
341
P EPL164 Epilepsy 72 0.040
342
c INF071 Inflammatory Bowel Disease 1 68 0.040
343
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.040
344
P HYP098 Hypereosinophilic Syndrome 66 0.040
345
c SML038 Small Cell Cancer of the Lung 66 0.040
346
P SPN046 Spinal Muscular Atrophy 64 0.040
347
NRM005 Neuromuscular Disease 64 0.040
348
ART002 Arts Syndrome 63 0.040
349
P MCH002 Machado-Joseph Disease 63 0.040
350
CLT003 Colitis 63 0.040
351
ALC006 Alcoholic Hepatitis 62 0.040
352
CNT105 Central Core Disease of Muscle 61 0.040
353
ATM095 Autoimmune Disease 61 0.040
354
P MYL006 Myeloid Leukemia 60 0.040
355
P VNT002 Ventricular Septal Defect 60 0.040
356
P BND020 Bone Disease 60 0.040
357
FBR047 Fibromyalgia 59 0.040
358
P OPT006 Optic Nerve Disease 58 0.040
359
IRN002 Iron Metabolism Disease 58 0.040
360
GST033 Gestational Diabetes 58 0.040
361
CLL003 Cellulitis 55 0.040
362
P ART021 Arteriosclerosis 55 0.040
363
P RCT021 Rectum Cancer 53 0.040
364
CRH005 Crohn's Colitis 53 0.040
365
ACR041 Acromelic Frontonasal Dysostosis 53 0.040
366
c PNT034 Pontocerebellar Hypoplasia, Type 2e 52 0.040
367
P MSC003 Muscular Atrophy 52 0.040
368
c VRL010 Viral Hepatitis 52 0.040
369
DNT012 Dental Caries 51 0.040
370
HRT011 Heart Septal Defect 51 0.040
371
HYP781 Hypoascorbemia 51 0.040
372
VCC001 Vaccinia 49 0.040
373
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.040
374
PLP001 Pulpitis 49 0.040
375
SLP001 Sleeping Sickness 49 0.040
376
P RNL015 Renal Hypertension 48 0.040
377
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.040
378
c PNT049 Pontocerebellar Hypoplasia, Type 2d 47 0.040
379
ATN005 Autonomic Dysfunction 47 0.040
380
INT067 Interstitial Nephritis 47 0.040
381
CRN019 Coronary Artery Vasospasm 47 0.040
383
c DRM054 Dermatitis, Atopic, 2 45 0.040
384
DWR001 Dwarfism 44 0.040
385
P MYG005 Myoglobinuria 44 0.040
386
GRW007 Growth Hormone Deficiency 43 0.040
387
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.040
388
ALL014 Allergic Encephalomyelitis 40 0.040
389
c GLC078 Glaucoma 1, Open Angle, F 36 0.040
390
NND010 Nondisjunction 35 0.040
391
BRT055 Breath-Holding Spells 30 0.040
392
URT049 Urate Oxidase, Pseudogene 25 0.040
393
DSC013 Discrimination, Two-Point, Reduction in 23 0.040
394
HYP188 Hypnic Headache 20 0.040
395
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.040
396
c SYS001 Systemic Lupus Erythematosus 87 0.032
397
c LKM061 Leukemia, Acute Myeloid 83 0.032
398
c DLT002 Dilated Cardiomyopathy 80 0.032
399
c LKM071 Leukemia, Chronic Lymphocytic 80 0.032
400
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.032
401
IMM167 Immune Deficiency Disease 78 0.032
402
CRV035 Cervical Cancer 76 0.032
403
ULC004 Ulcerative Colitis 73 0.032
404
P RTN024 Retinoblastoma 73 0.032
405
P FML011 Familial Adenomatous Polyposis 72 0.032
406
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.032
407
P PLM037 Pulmonary Hypertension 69 0.032
408
P HLP001 Holoprosencephaly 69 0.032
409
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.032
410
P LKM002 Leukemia 67 0.032
411
P HYP061 Hypertrophic Cardiomyopathy 67 0.032
412
c CHR684 Chronic Kidney Disease 67 0.032
413
P LNG028 Long Qt Syndrome 66 0.032
414
P PRS038 Personality Disorder 65 0.032
415
P MTR014 Motor Neuron Disease 65 0.032
416
PRP083 Porphyria, Acute Intermittent 64 0.032
417
P THR117 Three M Syndrome 1 64 0.032
418
P ORT004 Orthostatic Intolerance 63 0.032
419
P PRD008 Periodontitis 63 0.032
420
MSC152 Muscular Dystrophy, Becker Type 63 0.032
421
c ACT068 Acute Cystitis 63 0.032
422
P LMY004 Leiomyosarcoma 63 0.032
423
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 63 0.032
424
P RHB003 Rhabdomyosarcoma 63 0.032
425
MSS001 Masa Syndrome 62 0.032
426
P ESP024 Esophagitis 62 0.032
427
P PRP029 Porphyria 62 0.032
428
TXC005 Toxic Shock Syndrome 62 0.032
429
P KDN017 Kidney Cancer 61 0.032
430
PRT013 Portal Hypertension 61 0.032
431
VRC005 Varicose Veins 61 0.032
432
CHL068 Cholestasis 61 0.032
433
ING001 Inguinal Hernia 61 0.032
434
HPT019 Hepatic Encephalopathy 61 0.032
435
MCR013 Microphthalmia 61 0.032
436
ACQ007 Acquired Immunodeficiency Syndrome 60 0.032
437
PNM010 Pneumothorax, Primary Spontaneous 60 0.032
438
THY029 Thyroid Carcinoma 60 0.032
439
STT001 Status Epilepticus 60 0.032
440
CMP010 Complex Regional Pain Syndrome 59 0.032
441
EYD002 Eye Disease 59 0.032
442
PST028 Post-Traumatic Stress Disorder 59 0.032
443
P BCL017 B-Cell Lymphoma 58 0.032
444
CPR004 Coproporphyria, Hereditary 58 0.032
445
P RHN004 Rhinitis 58 0.032
446
P EXN002 Exanthem 58 0.032
447
SRC027 Sarcoma, Synovial 57 0.032
448
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.032
449
AGN016 Aging 56 0.032
450
c INT072 Intestinal Pseudo-Obstruction 56 0.032
451
PNM008 Pneumothorax 56 0.032
452
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.032
453
BRN004 Brain Edema 56 0.032
454
PRP082 Porphyria, Congenital Erythropoietic 56 0.032
455
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.032
456
NRL004 Neuroleptic Malignant Syndrome 56 0.032
457
ATR057 Atrioventricular Block 56 0.032
458
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 56 0.032
459
NRN004 Neuroendocrine Tumor 55 0.032
460
RSC001 Rosacea 55 0.032
461
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.032
462
P MYP006 Myopia 55 0.032
463
ISL014 Isolated Growth Hormone Deficiency, Type Ia 55 0.032
464
P LYM031 Lymphocytic Leukemia 55 0.032
465
END040 Endogenous Depression 55 0.032
466
P ANG015 Angioedema 54 0.032
467
HMS001 Hemosiderosis 54 0.032
468
GST009 Gastroschisis 54 0.032
469
AMN001 Amenorrhea 54 0.032
470
PRP016 Paraplegia 54 0.032
471
c FML008 Familial Retinoblastoma 53 0.032
472
GST023 Gastric Ulcer 53 0.032
473
NRT001 Neurotic Disorder 53 0.032
474
c MCR113 Microvascular Complications of Diabetes 3 53 0.032
475
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.032
476
PRG017 Paraganglioma and Gastric Stromal Sarcoma 53 0.032
477
PRS045 Prostatic Hypertrophy 52 0.032
478
ISL003 Isolated Growth Hormone Deficiency 52 0.032
479
NPH003 Nephrocalcinosis 52 0.032
480
HYP014 Hyperuricemia 52 0.032
481
PRS021 Prostatic Adenoma 51 0.032
482
THR004 Thrombocytosis 51 0.032
483
P TMP001 Temporal Lobe Epilepsy 51 0.032
484
BRX001 Bruxism 51 0.032
485
PTH003 Pathologic Nystagmus 51 0.032
486
STM007 Stomatitis 51 0.032
487
c INF145 Infantile Liver Failure Syndrome 1 50 0.032
488
NTR046 Neutrophil Migration 50 0.032
489
AMB002 Amblyopia 50 0.032
490
c ACT078 Acute Porphyria 50 0.032
491
PLC008 Placenta Disease 50 0.032
492
PRS129 Prostatic Hyperplasia, Benign 49 0.032
493
URM002 Uremia 49 0.032
494
QDR001 Quadriplegia 49 0.032
495
P OBS001 Obstructive Jaundice 49 0.032
496
SXL003 Sexual Disorder 48 0.032
497
ACT084 Acute Stress Disorder 48 0.032
498
ANV001 Anovulation 48 0.032
499
LPT006 Leptin Receptor Deficiency 47 0.032
500
ADR038 Adermatoglyphia 47 0.032
501
c MLG069 Malignant Hypertension 47 0.032
502
LYM019 Lymphosarcoma 47 0.032
503
RNL077 Renal Fibrosis 47 0.032
504
HST009 Histiocytoma 47 0.032
505
ACT113 Acute Myeloblastic Leukemia with Maturation 47 0.032
506
P PRP056 Porphyria, Acute Hepatic 47 0.032
507
P MYC033 Myoclonus 46 0.032
508
PLL012 Pollen Allergy 46 0.032
509
SYN036 Syncope 46 0.032
510
HDN002 Head Injury 46 0.032
511
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 46 0.032
512
KWS001 Kwashiorkor 45 0.032
513
INT071 Intestinal Perforation 45 0.032
514
NWC001 Newcastle Disease 45 0.032
515
MLG065 Malignant Fibroxanthoma 45 0.032
516
PRL008 Paralytic Ileus 45 0.032
517
ATN004 Autonomic Neuropathy 45 0.032
518
c CLR017 Clear Cell Sarcoma 44 0.032
519
OBS003 Obsessive-Compulsive Personality Disorder 44 0.032
520
DNT001 Dental Fluorosis 44 0.032
521
HPT004 Hepatic Coma 44 0.032
522
P MJR007 Major Affective Disorder 1 44 0.032
523
PRS063 Paresthesia 43 0.032
524
P END039 Endodermal Sinus Tumor 42 0.032
525
P LTH003 Lethal Congenital Contracture Syndrome 42 0.032
526
c ORT011 Orthostatic Hypotension 1 42 0.032
527
CLF056 Cleft Lip with or Without Cleft Palate 42 0.032
528
GST020 Gastric Antral Vascular Ectasia 42 0.032
529
VST004 Vestibular Disease 42 0.032
530
49X002 49,xxxxy Syndrome 42 0.032
531
P RRH023 Rare Hereditary Hemochromatosis 41 0.032
532
FBR003 Fibrous Histiocytoma 41 0.032
533
RDN001 Reading Disorder 41 0.032
534
ALX002 Alexithymia 39 0.032
535
TST018 Testicular Yolk Sac Tumor 39 0.032
536
LNG030 Lung Adenoma 39 0.032
537
ANG049 Angioedema Induced by Ace Inhibitors 39 0.032
538
SPP007 Suppression Amblyopia 39 0.032
539
c CHR682 Chronic Bilirubin Encephalopathy 39 0.032
540
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 39 0.032
541
HYP264 Hypertonia 39 0.032
542
PRR004 Preretinal Fibrosis 38 0.032
543
CTN011 Cutaneous Porphyria 38 0.032
544
P FML187 Familial Hypertension 37 0.032
545
GST004 Gastric Neuroendocrine Neoplasm 37 0.032
546
c PRX088 Paroxysmal Nonkinesigenic Dyskinesia 1 36 0.032
547
MTG002 Mutagen Sensitivity 36 0.032
548
PSD088 Pseudobulbar Affect 36 0.032
549
ABD010 Abdominal Wall Defect 35 0.032
550
CHR178 Chromosomal Triplication 35 0.032
551
PYR009 Pyridoxine Deficiency Anemia 35 0.032
552
c CHR064 Chronic Monocytic Leukemia 34 0.032
553
PRX035 Paroxysmal Dyskinesia 33 0.032
554
c PRS136 Prostate Cancer, Hereditary, 6 33 0.032
555
c PRS130 Prostate Cancer, Hereditary, 8 33 0.032
556
CRN270 Coronary Artery Dissection, Spontaneous 32 0.032
557
EXN003 Exencephaly 31 0.032
558
PLY150 Polykaryocytosis Inducer 31 0.032
559
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 0.032
560
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.032
561
c ORT012 Orthostatic Hypotension 2 27 0.032
562
BNG077 Benign Idiopathic Neonatal Seizures 27 0.032
563
ADG002 Audiogenic Seizures 26 0.032
564
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.032
565
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.032
566
ANT078 Antipyrine Metabolism 24 0.032
567
c DMN005 Diamond-Blackfan Anemia 2 23 0.032
568
INF043 Infantile Apnea 22 0.032
569
OBN001 Ouabain Resistance 19 0.032
570
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 14 0.032
571
ESP021 Esophageal Cancer 91 0.023
572
P RTT002 Rett Syndrome 81 0.023
573
INS024 Insulin-Like Growth Factor I 80 0.023
574
P LYN001 Lynch Syndrome 78 0.023
575
P MDL005 Medulloblastoma 78 0.023
576
P NRF023 Neurofibromatosis, Type Ii 77 0.023
577
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.023
578
c THR092 Thrombophilia Due to Thrombin Defect 73 0.023
579
P NJM001 Nijmegen Breakage Syndrome 73 0.023
580
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.023
581
c NRF024 Neurofibromatosis, Type I 72 0.023
582
GST040 Gastric Adenocarcinoma 71 0.023
583
PLM001 Pulmonary Tuberculosis 70 0.023
584
P TTR001 Tetralogy of Fallot 70 0.023
585
PLY001 Polycythemia Vera 70 0.023
586
WRN001 Werner Syndrome 70 0.023
587
LYM133 Lymphoma, Hodgkin, Classic 70 0.023
588
P MPL001 Maple Syrup Urine Disease 69 0.023
589
P HYP086 Hypothyroidism 69 0.023
590
P MYC084 Mycobacterium Tuberculosis 1 69 0.023
591
P LYM118 Lymphoma 69 0.023
592
RCK004 Rickets 69 0.023
593
P CRN037 Craniosynostosis 68 0.023
594
P MYS003 Myasthenia Gravis 68 0.023
595
P INF038 Influenza 68 0.023
596
P CLC063 Celiac Disease 1 68 0.023
597
P PNM007 Pneumonia 68 0.023
598
c ATS007 Autism Spectrum Disorder 68 0.023
599
KRT019 Keratitis, Hereditary 68 0.023
600
CRP001 Carpal Tunnel Syndrome 67 0.023
601
BLM001 Bloom Syndrome 67 0.023
602
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.023
603
P MCR115 Microvascular Complications of Diabetes 5 67 0.023
604
P CCK001 Cockayne Syndrome 67 0.023
605
c MCR129 Microvascular Complications of Diabetes 1 66 0.023
606
ANG054 Angina Pectoris 66 0.023
607
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.023
608
c PRD013 Periodic Fever, Familial, Autosomal Dominant 66 0.023
609
P MNN013 Meningitis 66 0.023
610
P LPS002 Liposarcoma 66 0.023
611
P ATS364 Autism 65 0.023
612
MYL031 Myeloproliferative Neoplasm 65 0.023
613
PRT036 Peritonitis 65 0.023
614
c WLM013 Wilms Tumor 1 65 0.023
615
P THY023 Thymoma 65 0.023
616
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.023
617
INC002 Inclusion Body Myositis 65 0.023
618
P ART005 Arteriovenous Malformation 65 0.023
619
CHY002 Chylomicron Retention Disease 65 0.023
620
NRF007 Neurofibroma 65 0.023
621
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.023
622
CLN015 Colon Adenocarcinoma 64 0.023
623
IRR002 Irritable Bowel Syndrome 64 0.023
624
IDP011 Idiopathic Interstitial Pneumonia 64 0.023
625
KHL003 Kohlschutter-Tonz Syndrome 64 0.023
626
NRF026 Neurofibromatosis, Type Iv, of Riccardi 64 0.023
627
c EPS035 Episodic Ataxia, Type 2 63 0.023
628
SKN016 Skin Disease 63 0.023
629
P NTR004 Neutropenia 63 0.023
630
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.023
631
P ART023 Arthropathy 63 0.023
632
P HYP055 Hypoplastic Left Heart Syndrome 63 0.023
633
c WLM018 Wilms Tumor 5 62 0.023
634
HMT002 Hematologic Cancer 62 0.023
635
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.023
636
P PLM036 Pulmonary Fibrosis 62 0.023
637
P CRG003 Crigler-Najjar Syndrome, Type I 62 0.023
638
BLD131 Bladder Urothelial Carcinoma 62 0.023
639
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.023
640
CRC021 Carcinosarcoma 62 0.023
641
P HYP750 Hypertriglyceridemia, Familial 62 0.023
642
P INT143 Interstitial Cystitis 62 0.023
643
P ENC004 Encephalitis 62 0.023
644
P LPS004 Lupus Erythematosus 61 0.023
645
VRL011 Viral Infectious Disease 61 0.023
646
P PNC044 Pancreatitis 61 0.023
647
P SNS001 Sensorineural Hearing Loss 61 0.023
648
NRL005 Neurilemmoma 61 0.023
649
P EPS003 Episodic Ataxia 61 0.023
650
P ATR010 Atrial Heart Septal Defect 61 0.023
651
CHR619 Chromosome 2q35 Duplication Syndrome 61 0.023
652
P ATS308 Autosomal Dominant Cerebellar Ataxia 61 0.023
653
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.023
654
DCB001 Decubitus Ulcer 60 0.023
655
INS001 Insulinoma 60 0.023
656
TRG002 Trigeminal Neuralgia 60 0.023
657
ORL011 Oral Cancer 60 0.023
658
P MYC008 Myocarditis 60 0.023
659
INT066 Interstitial Lung Disease 60 0.023
660
GNG013 Gingivitis 60 0.023
661
c ACT027 Acute Pancreatitis 60 0.023
662
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.023
663
c DNG003 Dengue Disease 60 0.023
664
c HPT016 Hepatitis B 60 0.023
665
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.023
666
PLM033 Pulmonary Embolism 59 0.023
667
VLV032 Vulva Cancer 59 0.023
668
P PLV020 Pelvic Organ Prolapse 59 0.023
669
c LYN004 Lynch Syndrome I 59 0.023
670
IRN001 Iron Deficiency Anemia 59 0.023
671
P GLL020 Gallbladder Disease 58 0.023
672
GLB001 Gilbert Syndrome 58 0.023
673
EMB004 Embryonal Carcinoma 58 0.023
674
P DNG005 Dengue Virus 58 0.023
675
P PRP019 Peripheral Nervous System Disease 58 0.023
676
P PRN023 Prion Disease 57 0.023
677
PLM031 Poliomyelitis 57 0.023
678
APH002 Aphasia 57 0.023
679
HMR039 Hemorrhage, Intracerebral 57 0.023
680
THR024 Thrombosis 57 0.023
681
SCH003 Schizophreniform Disorder 57 0.023
682
P NRP001 Neuropathy 57 0.023
683
ERY051 Erythroleukemia, Familial 57 0.023
684
P CHN012 Chondrosarcoma 57 0.023
685
PHR003 Pharyngitis 57 0.023
686
TRN018 Transitional Cell Carcinoma 57 0.023
687
PLS011 Plasmacytoma 57 0.023
688
BCT022 Bacterial Infectious Disease 56 0.023
689
ANN002 Anencephaly 56 0.023
690
ESP020 Esophageal Atresia 56 0.023
691
P MLN007 Male Infertility 56 0.023
692
AVN001 Avian Influenza 56 0.023
693
CMR002 Coumarin Resistance 56 0.023
694
P PLY011 Polycystic Ovary Syndrome 56 0.023
695
P MYS005 Myositis 56 0.023
696
GST050 Gastrointestinal System Disease 56 0.023
697
P PLM034 Pulmonary Emphysema 56 0.023
698
DFF005 Diffuse Large B-Cell Lymphoma 56 0.023
699
c SVR001 Severe Acute Respiratory Syndrome 56 0.023
700
TRD006 Tardive Dyskinesia 56 0.023
701
P FML012 Familial Partial Lipodystrophy 56 0.023
702
LMB062 Limb Ischemia 56 0.023
703
MCL006 Macular Retinal Edema 56 0.023
704
P PLY018 Polycythemia 56 0.023
705
P HYP076 Hyperthyroidism 56 0.023
706
P MYT023 Myotonia Congenita 56 0.023
707
CHL014 Cholera 56 0.023
708
c GRV008 Graves Disease 1 56 0.023
709
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.023
710
P FTL001 Fetal Alcohol Syndrome 55 0.023
711
VGN023 Vaginitis 55 0.023
712
CLF004 Cleft Lip/palate 55 0.023
713
P PTT006 Pituitary Adenoma 55 0.023
714
P MCR010 Microcephaly 55 0.023
715
JPN002 Japanese Encephalitis 54 0.023
716
P TCD001 Tic Disorder 54 0.023
717
P AGN002 Agnosia 54 0.023
718
P CYS039 Cystic Kidney Disease 54 0.023
719
c XRD030 Xeroderma Pigmentosum, Complementation Group C 54 0.023
720
c FML023 Familial Hemiplegic Migraine 54 0.023
721
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.023
722
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.023
723
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 54 0.023
724
MYM001 Myoma 54 0.023
725
BRN038 Bronchial Disease 54 0.023
726
HRT012 Heart Valve Disease 53 0.023
727
HMC014 Homocysteinemia 53 0.023
728
PRP080 Peripheral Artery Disease 53 0.023
729
P RTN018 Retinal Disease 53 0.023
730
PLS007 Plasmodium Falciparum Malaria 53 0.023
731
P INT068 Intestinal Disease 53 0.023
732
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.023
733
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.023
734
P PTS002 Ptosis 53 0.023
735
c THY107 Thymoma, Familial 53 0.023
736
OLG003 Oligohydramnios 52 0.023
737
THY124 Thyroid Gland Papillary Carcinoma 52 0.023
738
DSM007 Desmoplastic Small Round Cell Tumor 52 0.023
739
P PRR016 Pierre Robin Syndrome 52 0.023
740
ANK001 Ankylosis 52 0.023
741
CND002 Conduct Disorder 52 0.023
742
CHR005 Chorioamnionitis 52 0.023
743
P FBR031 Febrile Seizures 51 0.023
744
SPP010 Suppressor of Tumorigenicity 3 51 0.023
745
P HYP040 Hypospadias 51 0.023
746
PLR008 Pleurisy 51 0.023
747
CLR003 Clear Cell Adenocarcinoma 51 0.023
748
RTN003 Retinal Ischemia 51 0.023
749
HPT014 Hepatorenal Syndrome 51 0.023
750
c PNC106 Pancreatic Agenesis 1 51 0.023
751
P CHL066 Cholangitis 51 0.023
752
PRT029 Parathyroid Adenoma 51 0.023
753
CRN030 Coronary Stenosis 50 0.023
754
SYS003 Systolic Heart Failure 50 0.023
755
P OMP004 Omphalocele 50 0.023
756
HYP017 Hypophosphatemia 50 0.023
757
P EST001 Estrogen-Receptor Positive Breast Cancer 50 0.023
758
FDL002 Food Allergy 50 0.023
759
P MYT002 Myotonic Dystrophy 50 0.023
760
CHL004 Cholelithiasis 50 0.023
761
c HNT004 Huntington Disease-Like 2 49 0.023
762
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 49 0.023
763
HYL004 Hyaline Fibromatosis Syndrome 49 0.023
764
c DYS119 Dystonia 9 49 0.023
765
CLN045 Colonic Benign Neoplasm 49 0.023
766
HPT009 Hepatopulmonary Syndrome 49 0.023
767
KRT002 Keratomalacia 49 0.023
768
NRL018 Neural Tube Defects, Folate-Sensitive 49 0.023
769
P EPT012 Epithelioid Sarcoma 49 0.023
770
c XRD032 Xeroderma Pigmentosum, Complementation Group B 49 0.023
771
DBT006 Diabetic Macular Edema 49 0.023
772
P BRS053 Breast Fibroadenoma 48 0.023
773
c SCH079 Schizophrenia 1 48 0.023
774
SPL018 Splenomegaly 48 0.023
775
PRD004 Prediabetes Syndrome 48 0.023
776
P ENC008 Encephalocele 48 0.023
777
c MCR120 Microvascular Complications of Diabetes 7 47 0.023
778
c CRN241 Corneal Dystrophy, Congenital Stromal 47 0.023
779
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.023
780
UMB002 Umbilical Hernia 47 0.023
781
NDL013 Nodular Regenerative Hyperplasia 47 0.023
782
P CRC039 Coarctation of Aorta 47 0.023
783
SRT004 Serotonin Syndrome 47 0.023
784
PNC034 Pancreas Disease 47 0.023
785
RCT020 Rectum Adenocarcinoma 47 0.023
786
KRT013 Keratolytic Winter Erythema 46 0.023
787
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.023
788
MNN032 Meningococcal Meningitis 46 0.023
789
TRT001 Teratocarcinoma 46 0.023
790
ACT055 Actinomycosis 46 0.023
791
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 46 0.023
792
RTR008 Root Resorption 46 0.023
793
HRN026 Hernia, Hiatus 46 0.023
794
P BNG032 Benign Mesothelioma 45 0.023
795
c MLG068 Malignant Glioma 45 0.023
796
GLC022 Glucose/galactose Malabsorption 45 0.023
797
MTS001 Mutism 45 0.023
798
RTR001 Retrograde Amnesia 45 0.023
799
HYP034 Hypertensive Encephalopathy 45 0.023
800
OLG001 Oligospermia 45 0.023
801
P HMP006 Hemiplegic Migraine 45 0.023
802
CRB004 Cerebral Artery Occlusion 45 0.023
803
ACT029 Acute Interstitial Pneumonia 45 0.023
804
CRB025 Carbohydrate Metabolic Disorder 45 0.023
805
PRM003 Premature Ejaculation 44 0.023
806
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.023
807
IMM064 Immunodeficiency, Common Variable, 10 44 0.023
808
CRT015 Carotid Artery Occlusion 44 0.023
809
c HYP272 Hypercholesterolemia, Familial, 3 44 0.023
810
DMP001 Dumping Syndrome 44 0.023
811
CRB090 Cerebral Hypoxia 44 0.023
812
c ADV003 Advanced Sleep Phase Syndrome, Familial, 1 43 0.023
813
PLY068 Polysubstance Abuse 43 0.023
814
P CLS010 Cluster Headache 43 0.023
815
BNS007 Bone Sarcoma 43 0.023
816
DRG002 Drug-Induced Hepatitis 43 0.023
817
c SPR086 Spermatogenic Failure 3 42 0.023
818
MCR103 Microtia 42 0.023
819
TRP014 Triploidy 42 0.023
820
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.023
821
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.023
822
MMM006 Mammographic Density 42 0.023
823
c MCR130 Microvascular Complications of Diabetes 6 41 0.023
824
c MCR133 Microvascular Complications of Diabetes 4 41 0.023
825
P HYP263 Hypersomnia 41 0.023
826
c CHR579 Chiari Malformation Type Ii 41 0.023
827
ACT088 Acute Insulin Response 41 0.023
828
P RRT020 Rare Tumor 41 0.023
829
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.023
830
HYP540 Hypertension, Diastolic 41 0.023
831
EXT006 Extrahepatic Cholestasis 41 0.023
832
GLC008 Glucose Metabolism Disease 41 0.023
833
P CHR342 Chiari Malformation 41 0.023
834
AMP007 Amphetamine Abuse 40 0.023
835
INT060 Intestinal Atresia 40 0.023
836
CRD005 Cardia Cancer 40 0.023
837
SPS057 Spasticity 40 0.023
838
SPR126 Superior Semicircular Canal Dehiscence 40 0.023
839
P TRC031 Trichorhinophalangeal Syndrome 40 0.023
840
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.023
841
MLT001 Multiple Chemical Sensitivity 39 0.023
842
BKR002 Baker-Gordon Syndrome 39 0.023
843
DSN001 De Sanctis-Cacchione Syndrome 39 0.023
844
FNC002 Functional Diarrhea 39 0.023
845
CNN001 Cannabis Dependence 39 0.023
846
SCR011 Scrapie 39 0.023
847
DPR002 Depersonalization Disorder 38 0.023
848
c HNT011 Huntington Disease-Like 3 38 0.023
849
HYP026 Hypoglycemic Coma 38 0.023
850
HYP835 Hypothalamic Obesity 38 0.023
851
c HMG029 Hemoglobin Se Disease 38 0.023
852
OCL010 Ocular Hypotension 38 0.023
853
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.023
854
PST029 Postmenopausal Atrophic Vaginitis 38 0.023
855
c BLP048 Blepharospasm, Benign Essential 38 0.023
856
HRN029 Hearing Loss, Noise-Induced 37 0.023
857
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 37 0.023
858
CRD245 Cardiac-Urogenital Syndrome 36 0.023
859
WHP002 Whiplash 36 0.023
860
P FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 36 0.023
861
TTH004 Tethered Spinal Cord Syndrome 36 0.023
863
MYT011 Myotonia 36 0.023
864
DNT008 Denture Stomatitis 36 0.023
865
PLM028 Pulmonary Coin Lesion 35 0.023
866
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 35 0.023
867
c MJR008 Major Affective Disorder 2 35 0.023
868
c MCR312 Microphthalmia, Syndromic 10 35 0.023
869
SPR017 Spermatocele 34 0.023
870
c RST012 Restless Legs Syndrome 1 34 0.023
871
P EXT032 Extraosseous Osteosarcoma 34 0.023
872
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 34 0.023
873
c CLR066 Ciliary Dyskinesia, Primary, 2 34 0.023
874
NSL006 Nasal Cavity Squamous Cell Carcinoma 34 0.023
875
c MJR003 Major Affective Disorder 6 33 0.023
876
c MJR006 Major Affective Disorder 5 33 0.023
877
c PRG003 Progesterone-Receptor Negative Breast Cancer 33 0.023
878
MTB016 Metabolic Myopathy 33 0.023
879
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.023
880
HND015 Hand Skill, Relative 33 0.023
881
c MJR023 Major Affective Disorder 7 33 0.023
882
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.023
883
c LCL022 Localized Lipodystrophy 32 0.023
884
RRS014 Rare Surgical Neurologic Disease 32 0.023
885
c FBR070 Febrile Seizures, Familial, 8 31 0.023
886
PRT006 Partial Motor Epilepsy 31 0.023
887
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 31 0.023
888
GST007 Gastric Dilatation 31 0.023
889
LMB010 Lambert Syndrome 30 0.023
890
GRN004 Granulomatous Amebic Encephalitis 29 0.023
891
c MJR004 Major Affective Disorder 4 29 0.023
892
FCT008 Factitious Disorder 28 0.023
893
c MLG151 Malignant Hyperthermia 5 28 0.023
894
c TRC073 Treacher Collins Syndrome 2 27 0.023
895
ENM002 Enamel Erosion 27 0.023
896
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.023
897
IMM002 Immature Cataract 25 0.023
898
NN2002 Non 24 Hour Sleep Wake Disorder 24 0.023
899
DSS025 Dissociative Seizures 24 0.023
900
CLN012 Colon Leiomyosarcoma 24 0.023
901
SML003 Small Cell Osteogenic Sarcoma 24 0.023
902
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 24 0.023
903
PRX022 Paroxysmal Choreoathetosis 23 0.023
904
P SLF001 Sulfhemoglobinemia 23 0.023
905
SDD004 Sudden Arrhythmia Death Syndrome 23 0.023
906
c PRX024 Paroxysmal Nonkinesigenic Dyskinesia 2 21 0.023
907
c MYP040 Myopia 7 20 0.023
908
BDR001 Bidirectional Tachycardia 19 0.023
909
STN005 St Anthony's Fire 17 0.023
910
FRC013 Fructose Utilization 15 0.023
911
DGT004 Digitalis Poisoning 14 0.023
912
NRL025 Neural Tube Closure Defect 12 0.023
913
PRX087 Paroxysomal Nonkinesigenic Dyskinesia 2 0.023
Content
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