Search results for opioids

1669 hits were found for opioids

# Family MCID Name MIFTS Score
1
OPT003 Opiate Dependence 50 6.713
2
OPD001 Opioid Abuse 46 6.361
3
OPD004 Opioid Dependence 1 16 5.728
4
INC030 Increased Analgesia from Kappa-Opioid Receptor Agonist, Female-Specific 14 5.177
5
OPD006 Opioid Addiction 48 4.393
6
ACT171 Acute Opioid Poisoning 6 2.367
7
P CHR345 Chronic Pain 44 0.913
8
PNG002 Pain Agnosia 51 0.829
9
CNS004 Constipation 58 0.577
10
P SBS003 Substance Abuse 55 0.513
11
c PNS012 Paine Syndrome 61 0.421
12
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.419
13
PRT037 Pertussis 65 0.370
14
WTH001 Withdrawal Disorder 48 0.328
15
BCK006 Back Pain 42 0.315
16
ALC007 Alcohol Dependence 66 0.299
17
P NRB001 Neuroblastoma 72 0.281
18
DPR016 Depression 63 0.273
19
NNT008 Neonatal Abstinence Syndrome 41 0.269
20
P ALC033 Alcohol Use Disorder 58 0.247
21
ANX010 Anxiety 73 0.246
22
DRG003 Drug Dependence 47 0.241
23
MNT002 Mental Depression 58 0.233
24
48X005 48,xyyy 39 0.221
25
HRN003 Heroin Dependence 44 0.202
26
P SLP006 Sleep Apnea 69 0.199
27
OST012 Osteoarthritis 78 0.193
28
ILS001 Ileus 51 0.191
29
MDD011 Mood Disorder 62 0.183
30
FBR047 Fibromyalgia 58 0.182
31
SBC016 Subacute Delirium 44 0.175
32
P PRS038 Personality Disorder 65 0.174
33
P GLM045 Glioma 63 0.172
34
c HPT073 Hepatitis C Virus 72 0.171
35
c HPT001 Hepatitis C 62 0.170
36
SBS004 Substance Dependence 48 0.167
37
c MGR028 Migraine with or Without Aura 1 67 0.166
38
P SZR006 Seizure Disorder 56 0.165
39
HYP080 Hypogonadism 50 0.162
40
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.161
41
P MJR001 Major Depressive Disorder 68 0.157
42
ALL026 Allergic Hypersensitivity Disease 62 0.157
43
VSL002 Visual Epilepsy 59 0.157
44
P SCK005 Sickle Cell Disease 50 0.156
45
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.153
46
P DRR001 Diarrhea 55 0.152
47
CCN001 Cocaine Dependence 48 0.150
48
GLL048 Glial Tumor 45 0.149
49
P NRP001 Neuropathy 56 0.148
50
CHL014 Cholera 59 0.147
51
P HDC001 Headache 57 0.147
52
HYP266 Hypoxia 57 0.147
53
MRP001 Morphine Dependence 41 0.147
54
P RSP003 Respiratory Failure 74 0.137
55
DSS008 Disease of Mental Health 58 0.137
56
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.137
57
CCN002 Cocaine Abuse 49 0.137
58
PLY068 Polysubstance Abuse 43 0.137
59
c RHB024 Rhabdomyosarcoma 2 67 0.131
60
TBC004 Tobacco Addiction 64 0.131
61
PST028 Post-Traumatic Stress Disorder 58 0.131
62
CHL068 Cholestasis 61 0.130
63
47X002 47,xyy 49 0.130
64
PSY004 Psychotic Disorder 67 0.128
65
SPN186 Spinal Cord Injury 60 0.127
66
ACT084 Acute Stress Disorder 47 0.127
67
ISC004 Ischemia 58 0.123
68
P MYC033 Myoclonus 46 0.123
69
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.123
70
HMN044 Human Immunodeficiency Virus Type 1 71 0.116
71
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.115
72
P BPL003 Bipolar Disorder 56 0.115
73
DBT010 Diabetic Neuropathy 54 0.115
74
SXL003 Sexual Disorder 47 0.115
75
HYP056 Hypoglycemia 66 0.114
76
ATX019 Ataxia with Vitamin E Deficiency 42 0.114
77
P HPT021 Hepatitis 67 0.112
78
P SCL018 Scoliosis 60 0.112
79
ACQ007 Acquired Immunodeficiency Syndrome 60 0.112
80
ETN001 Eating Disorder 60 0.112
81
IRR002 Irritable Bowel Syndrome 65 0.111
82
AVD001 Avoidant Personality Disorder 51 0.111
83
c MJR024 Major Affective Disorder 9 41 0.111
84
c MJR022 Major Affective Disorder 8 38 0.111
85
P BRS047 Breast Cancer 97 0.110
86
P LVR013 Liver Disease 68 0.110
87
ING001 Inguinal Hernia 60 0.105
88
P TRM003 Tremor 54 0.105
90
P SLP005 Sleep Disorder 59 0.104
91
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.102
92
ADL002 Adult Syndrome 70 0.102
93
P INF037 Inflammatory Bowel Disease 54 0.102
94
BRN071 Brain Injury 49 0.102
95
CYT002 Cytokine Deficiency 42 0.102
96
P KDN018 Kidney Disease 72 0.101
97
SQM006 Squamous Cell Carcinoma 60 0.101
98
P END033 Endocarditis 57 0.101
99
AMN003 Amnestic Disorder 54 0.101
100
P RST001 Restless Legs Syndrome 54 0.101
101
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.101
102
P LNG032 Lung Cancer 98 0.099
103
P ART022 Arthritis 69 0.099
104
P CRD119 Cardiac Arrest 67 0.099
105
P PRP019 Peripheral Nervous System Disease 58 0.099
106
P TRN020 Turner Syndrome 67 0.098
107
OCL069 Ocular Motor Apraxia 51 0.098
108
P CLR023 Colorectal Cancer 99 0.096
109
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.096
110
LVR012 Liver Cirrhosis 62 0.096
111
CRB004 Cerebral Artery Occlusion 45 0.096
112
ANR007 Anorexia Nervosa 63 0.094
113
P BNC003 Bone Cancer 58 0.094
114
c CNT015 Central Sleep Apnea 45 0.094
115
P PNC035 Pancreatic Cancer 84 0.093
116
P ATS364 Autism 70 0.093
117
DWN001 Down Syndrome 70 0.093
118
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.093
119
P PNC044 Pancreatitis 61 0.093
120
GNR004 Generalized Anxiety Disorder 56 0.093
121
BRD004 Borderline Personality Disorder 53 0.093
122
HLX001 Helix Syndrome 47 0.093
123
END040 Endogenous Depression 55 0.091
124
AMN001 Amenorrhea 54 0.091
125
P PNC025 Panic Disorder 53 0.091
126
TRM010 Traumatic Brain Injury 51 0.091
127
IMM167 Immune Deficiency Disease 78 0.089
128
CNG034 Congestive Heart Failure 69 0.089
129
P ENC018 Encephalopathy 61 0.089
130
c ACT027 Acute Pancreatitis 60 0.089
131
IDP070 Idiopathic Scoliosis 42 0.089
132
P PHC003 Pheochromocytoma 71 0.088
133
HYP066 Hyperglycemia 61 0.088
134
GST050 Gastrointestinal System Disease 56 0.088
135
ADR040 Adrenal Gland Pheochromocytoma 46 0.088
136
PST053 Postherpetic Neuralgia 40 0.088
137
c HYP595 Hypertension, Essential 84 0.086
138
P RHM011 Rheumatoid Arthritis 80 0.086
139
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.086
140
P PLY011 Polycystic Ovary Syndrome 56 0.086
141
NRT001 Neurotic Disorder 53 0.086
142
P INT068 Intestinal Disease 53 0.086
143
MCN017 Meconium Ileus 52 0.086
144
P SCH015 Schizophrenia 74 0.084
145
P CNR004 Cone-Rod Dystrophy 2 73 0.084
146
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.084
147
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.084
148
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.084
149
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.084
150
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.084
151
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.084
152
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.084
153
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.084
154
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.084
155
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.084
156
P ALZ034 Alzheimer Disease 88 0.082
157
MCS002 Mucositis 56 0.082
158
INF034 Infective Endocarditis 53 0.082
159
c VRL010 Viral Hepatitis 52 0.082
160
IMP005 Impotence 52 0.082
161
APN008 Apnea, Obstructive Sleep 64 0.080
162
c FNC043 Fanconi Anemia, Complementation Group E 62 0.080
163
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.080
164
ANT011 Antisocial Personality Disorder 47 0.080
165
c HPT003 Hepatitis a 62 0.078
166
NPH009 Nephrolithiasis 55 0.078
167
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.076
168
SCK003 Sickle Cell Anemia 74 0.074
169
CRH001 Crohn's Disease 74 0.074
170
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.074
171
CMP010 Complex Regional Pain Syndrome 58 0.074
172
CVD001 Covid-19 44 0.074
173
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.074
174
CHL079 Children's Interstitial Lung Disease 26 0.074
175
SVR004 Severe Combined Immunodeficiency 73 0.072
176
P THY023 Thymoma 65 0.072
177
P END044 Endometriosis 63 0.072
178
CLT003 Colitis 62 0.072
179
c THY107 Thymoma, Familial 52 0.072
180
DYS073 Dysphagia 50 0.072
181
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.072
182
ANX004 Anoxia 40 0.072
183
CNN001 Cannabis Dependence 40 0.072
184
P ART023 Arthropathy 62 0.070
185
P PLY019 Polyneuropathy 56 0.070
186
P AGN002 Agnosia 55 0.070
187
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.070
188
P SCL057 Scoliosis, Isolated 1 41 0.070
189
ALL014 Allergic Encephalomyelitis 38 0.070
190
P OVR042 Ovarian Cancer 88 0.068
191
P PRK057 Parkinson Disease, Late-Onset 78 0.068
192
P HRT032 Heart Disease 75 0.068
193
LPT014 Leptin Deficiency or Dysfunction 74 0.068
194
c CHR684 Chronic Kidney Disease 70 0.068
195
TRG002 Trigeminal Neuralgia 60 0.068
196
HPT019 Hepatic Encephalopathy 60 0.068
197
PLM010 Pulmonary Edema 54 0.068
198
SRT004 Serotonin Syndrome 47 0.068
199
HDN002 Head Injury 46 0.068
200
HPT004 Hepatic Coma 45 0.068
201
P HPT023 Hepatocellular Carcinoma 100 0.066
202
P PRS040 Prostate Cancer 97 0.066
203
P DMN002 Dementia 66 0.066
204
P DYS154 Dystonia 65 0.066
205
APP008 Appendicitis 61 0.066
206
LNG099 Lung Disease 60 0.066
207
P INF032 Infertility 57 0.066
208
SPN019 Spondylolisthesis 51 0.066
209
P TMP001 Temporal Lobe Epilepsy 50 0.066
210
P CMP008 Compartment Syndrome 49 0.066
211
CYT018 Cytochrome P450 2d6 Variant 27 0.066
212
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.066
213
P OST002 Osteoporosis 74 0.063
214
P EPL164 Epilepsy 71 0.063
215
P MYC007 Myocardial Infarction 70 0.063
216
DFC004 Deficiency Anemia 70 0.063
217
PNM008 Pneumothorax 56 0.063
218
GST037 Gastroparesis 54 0.063
219
PTH003 Pathologic Nystagmus 52 0.063
220
SYN036 Syncope 45 0.063
221
SPS057 Spasticity 45 0.063
222
ENT001 Enterocele 39 0.063
223
c ATS007 Autism Spectrum Disorder 67 0.061
224
P DRM053 Dermatitis, Atopic 66 0.061
225
P ADN016 Adenocarcinoma 64 0.061
226
HYP020 Hyperprolactinemia 64 0.061
227
ATM095 Autoimmune Disease 62 0.061
228
DRM006 Dermatitis 61 0.061
229
VRL011 Viral Infectious Disease 61 0.061
230
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.061
231
EMB004 Embryonal Carcinoma 56 0.061
232
BRN004 Brain Edema 56 0.061
233
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.061
234
TRD006 Tardive Dyskinesia 54 0.061
235
ACH005 Achalasia 51 0.061
236
END086 End Stage Renal Disease 51 0.061
237
DYS009 Dysthymic Disorder 49 0.061
238
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.061
239
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.061
240
URM005 Uremic Pruritus 42 0.061
241
MYL069 Myeloma, Multiple 85 0.058
242
STR067 Stroke, Ischemic 81 0.058
243
P MLN008 Melanoma 69 0.058
244
OBS002 Obsessive-Compulsive Disorder 68 0.058
245
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.058
246
STT001 Status Epilepticus 60 0.058
247
P PLV020 Pelvic Organ Prolapse 57 0.058
248
AGN016 Aging 56 0.058
249
P PTS002 Ptosis 53 0.058
250
PRP016 Paraplegia 52 0.058
251
CND002 Conduct Disorder 51 0.058
252
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.058
253
PTT037 Pituitary Tumors 44 0.058
254
CNN002 Cannabis Abuse 44 0.058
255
TRP009 Triple X Syndrome 42 0.058
256
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.058
257
BNN005 Bunion 33 0.058
258
P BLD134 Bladder Cancer 79 0.055
259
P LYM118 Lymphoma 68 0.055
260
P PNM007 Pneumonia 68 0.055
261
PNC129 Pancreatic Adenocarcinoma 68 0.055
262
P VSC007 Vascular Disease 63 0.055
263
SKN016 Skin Disease 63 0.055
264
P MVM001 Movement Disease 63 0.055
265
c SVR001 Severe Acute Respiratory Syndrome 62 0.055
266
NTR005 Nutritional Deficiency Disease 62 0.055
267
P INT143 Interstitial Cystitis 61 0.055
268
HRP004 Herpes Zoster 60 0.055
269
c ACT071 Acute Kidney Failure 60 0.055
270
SPN027 Spinal Stenosis 59 0.055
271
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.055
272
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.055
273
c ACT134 Acute Liver Failure 56 0.055
274
HYP060 Hyperinsulinism 54 0.055
275
RDC002 Radiculopathy 50 0.055
276
PST021 Postpartum Depression 50 0.055
277
PTH002 Pathological Gambling 49 0.055
278
UMB002 Umbilical Hernia 46 0.055
279
MNN017 Mononeuropathy 42 0.055
280
MYF002 Myofascial Pain Syndrome 42 0.055
281
NRL016 Neural Tube Defects 82 0.053
282
c SPN225 Spondyloarthropathy 1 73 0.053
283
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.053
284
P BRG001 Brugada Syndrome 71 0.053
285
GLL008 Gilles De La Tourette Syndrome 66 0.053
286
c SML038 Small Cell Cancer of the Lung 65 0.053
287
PRT036 Peritonitis 64 0.053
288
TXC005 Toxic Shock Syndrome 62 0.053
289
SDD001 Sudden Infant Death Syndrome 61 0.053
290
PNM010 Pneumothorax, Primary Spontaneous 60 0.053
291
PPT005 Peptic Ulcer Disease 59 0.053
292
P EXN002 Exanthem 57 0.053
293
RFL001 Reflex Sympathetic Dystrophy 54 0.053
294
MTN003 Motion Sickness 53 0.053
295
TXC002 Toxic Encephalopathy 53 0.053
296
DBT004 Diabetic Polyneuropathy 49 0.053
297
PCT003 Pectus Excavatum 49 0.053
298
SCL003 Social Phobia 48 0.053
299
c DRR009 Diarrhea 6 46 0.053
300
URL001 Urolithiasis 45 0.053
301
LWC001 Low Compliance Bladder 43 0.053
302
PRM020 Premenstrual Tension 40 0.053
303
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.053
304
CRV035 Cervical Cancer 76 0.050
305
c ATR087 Atrial Standstill 1 75 0.050
306
ULC004 Ulcerative Colitis 73 0.050
307
P LKM062 Leukemia, Acute Lymphoblastic 69 0.050
308
P LKM002 Leukemia 68 0.050
309
CRB039 Cerebrovascular Disease 67 0.050
310
c MCR129 Microvascular Complications of Diabetes 1 66 0.050
311
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.050
312
P CYS018 Cystitis 59 0.050
313
ADN018 Adenoma 59 0.050
314
P BCL017 B-Cell Lymphoma 58 0.050
315
CHL067 Cholecystitis 57 0.050
316
P RHN004 Rhinitis 57 0.050
317
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.050
318
P STR020 Strabismus 55 0.050
319
PTT009 Pituitary Gland Disease 54 0.050
320
INT075 Intracranial Hypertension 53 0.050
321
P HYP730 Hypogonadotropic Hypogonadism 52 0.050
322
P DDN001 Duodenal Ulcer 52 0.050
323
DGN001 Degenerative Disc Disease 48 0.050
324
CRT015 Carotid Artery Occlusion 45 0.050
325
PRM003 Premature Ejaculation 44 0.050
326
c PRM038 Primary Agammaglobulinemia 44 0.050
327
CRB090 Cerebral Hypoxia 44 0.050
328
P CLS010 Cluster Headache 42 0.050
329
MCH006 Mechanical Strabismus 42 0.050
330
RDN001 Reading Disorder 40 0.050
331
c PRS136 Prostate Cancer, Hereditary, 6 33 0.050
332
c PRS130 Prostate Cancer, Hereditary, 8 32 0.050
333
c LKM061 Leukemia, Acute Myeloid 84 0.046
334
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.046
335
LYM133 Lymphoma, Hodgkin, Classic 69 0.046
336
P HYP086 Hypothyroidism 69 0.046
337
ART016 Aortic Aneurysm 69 0.046
338
P PLM037 Pulmonary Hypertension 67 0.046
339
P CLC063 Celiac Disease 1 66 0.046
340
OST159 Osteogenic Sarcoma 66 0.046
341
ANG054 Angina Pectoris 66 0.046
342
TTN003 Tetanus 65 0.046
343
P HRP006 Herpes Simplex 65 0.046
344
P DBT009 Diabetes Mellitus 64 0.046
345
GT001 Gout 64 0.046
346
PLG002 Plague 63 0.046
347
P PSR002 Psoriasis 62 0.046
348
P MYL006 Myeloid Leukemia 60 0.046
349
CRD223 Cardiac Arrhythmia 60 0.046
350
c HPT016 Hepatitis B 59 0.046
351
c ACT073 Acute Leukemia 58 0.046
352
P URT039 Urticaria 58 0.046
353
BLM002 Bulimia Nervosa 57 0.046
354
c ACT075 Acute Myocardial Infarction 57 0.046
355
P MLN007 Male Infertility 55 0.046
356
CLF001 Cleft Lip 53 0.046
357
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.046
358
PST011 Pustulosis of Palm and Sole 52 0.046
359
SPN051 Spondylitis 51 0.046
360
P AST007 Astrocytoma 51 0.046
361
c BPL002 Bipolar I Disorder 49 0.046
362
RTR001 Retrograde Amnesia 44 0.046
363
DMP001 Dumping Syndrome 44 0.046
364
49X006 49, Xxxxy Syndrome 41 0.046
365
PRS063 Paresthesia 41 0.046
366
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.046
367
SPR126 Superior Semicircular Canal Dehiscence 40 0.046
368
c HMG029 Hemoglobin Se Disease 39 0.046
369
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.046
370
PRR013 Prurigo Nodularis 36 0.046
371
c SCN052 Secondary Adrenal Insufficiency 36 0.046
372
HRW001 Hair Whorl 36 0.046
373
INF009 Inflammatory Spondylopathy 31 0.046
374
PLY150 Polykaryocytosis Inducer 31 0.046
375
PRS120 Persistent Idiopathic Facial Pain 28 0.046
376
AST005 Asthma 76 0.043
377
PRP027 Peripheral Vascular Disease 71 0.043
378
P AMY004 Amyloidosis 70 0.043
379
MYL009 Myelodysplastic Syndrome 70 0.043
380
CRB037 Cerebral Palsy 69 0.043
381
P OCL013 Oculodentodigital Dysplasia 69 0.043
382
CRP001 Carpal Tunnel Syndrome 67 0.043
383
MYC006 Mycosis Fungoides 66 0.043
384
c MCL013 Mucolipidosis Iv 66 0.043
385
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.043
386
P ANR048 Aniridia 1 63 0.043
387
P BRS044 Breast Adenocarcinoma 59 0.043
388
ANR040 Aneurysm 59 0.043
389
P ANP001 Anaplastic Large Cell Lymphoma 58 0.043
390
SPT004 Septic Arthritis 58 0.043
391
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.043
392
P CRD246 Cardiovascular System Disease 57 0.043
393
CHR100 Chronic Ulcer of Skin 55 0.043
394
P DBT005 Diabetes Insipidus 55 0.043
395
HRY003 Hairy Cell Leukemia 55 0.043
396
CLF004 Cleft Lip/palate 54 0.043
397
SYN007 Synovitis 54 0.043
398
CLL003 Cellulitis 54 0.043
399
P TCD001 Tic Disorder 53 0.043
400
ART140 Arteries, Anomalies of 52 0.043
401
P NRC002 Narcolepsy 52 0.043
402
PLS009 Plasma Cell Neoplasm 51 0.043
403
ENT004 Enthesopathy 49 0.043
404
ASP007 Aspiration Pneumonia 48 0.043
405
P MJR007 Major Affective Disorder 1 43 0.043
406
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.043
407
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.043
408
c CHR682 Chronic Bilirubin Encephalopathy 39 0.043
409
PLC002 Plica Syndrome 36 0.043
410
EPD005 Epidural Abscess 35 0.043
411
PPL052 Papillomatosis, Confluent and Reticulated 33 0.043
412
ADG002 Audiogenic Seizures 25 0.043
413
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.043
414
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.039
415
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.039
416
P GST053 Gastric Cancer 83 0.039
417
P LKM071 Leukemia, Chronic Lymphocytic 79 0.039
418
KPS004 Kaposi Sarcoma 75 0.039
419
GLB015 Glioblastoma Multiforme 75 0.039
420
c THR092 Thrombophilia Due to Thrombin Defect 73 0.039
421
P MLT020 Multiple Sclerosis 72 0.039
422
c LKM063 Leukemia, Chronic Myeloid 72 0.039
423
MYL005 Myelofibrosis 70 0.039
424
PLY001 Polycythemia Vera 69 0.039
425
MST024 Mastocytosis, Cutaneous 69 0.039
426
MNT001 Mantle Cell Lymphoma 69 0.039
427
P ESS003 Essential Thrombocythemia 68 0.039
428
BRN024 Bronchitis 68 0.039
429
GST092 Gastroesophageal Reflux 67 0.039
430
BRK010 Burkitt Lymphoma 67 0.039
431
P FLL037 Follicular Lymphoma 67 0.039
432
P HYD006 Hydrocephalus 66 0.039
433
MYL031 Myeloproliferative Neoplasm 66 0.039
434
P NRV007 Nervous System Disease 66 0.039
435
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.039
436
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.039
437
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.039
438
OST017 Osteomyelitis 64 0.039
439
P CRN300 Coronary Heart Disease 1 63 0.039
440
c ACT068 Acute Cystitis 63 0.039
441
LPD008 Lipid Metabolism Disorder 62 0.039
442
LPP008 Lipoprotein Quantitative Trait Locus 62 0.039
443
P TRC086 Trichohepatoenteric Syndrome 1 62 0.039
444
WLD007 Waldenstroem's Macroglobulinemia 61 0.039
445
P KDN017 Kidney Cancer 60 0.039
446
SZR001 Sezary's Disease 60 0.039
447
DPH001 Diphtheria 60 0.039
448
ACN002 Acanthosis Nigricans 60 0.039
449
ORL011 Oral Cancer 60 0.039
450
P CHR285 Chronic Myelomonocytic Leukemia 60 0.039
451
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.039
452
PLM033 Pulmonary Embolism 59 0.039
453
PRT058 Pure Autonomic Failure 59 0.039
454
P LYM033 Lymphoproliferative Syndrome 59 0.039
455
P GLL022 Guillain-Barre Syndrome 59 0.039
456
CRD132 Cardiac Conduction Defect 58 0.039
457
CNT047 Contact Dermatitis 58 0.039
458
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.039
459
P GLL020 Gallbladder Disease 57 0.039
460
GLS018 Glass Syndrome 57 0.039
461
STR081 Stormorken Syndrome 57 0.039
462
P PLY018 Polycythemia 56 0.039
463
P FBR017 Fibrosarcoma 56 0.039
464
PLS011 Plasmacytoma 56 0.039
465
ATR057 Atrioventricular Block 55 0.039
466
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.039
467
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.039
468
FCL014 Focal Epilepsy 54 0.039
469
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.039
470
THR013 Thoracic Outlet Syndrome 54 0.039
471
LYM040 Lymphoblastic Lymphoma 54 0.039
472
PST046 Post-Transplant Lymphoproliferative Disease 53 0.039
473
FNG017 Fungal Infectious Disease 53 0.039
474
c GLL024 Gallbladder Disease 1 53 0.039
475
CHR073 Choreatic Disease 52 0.039
476
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.039
477
MRG003 Marginal Zone B-Cell Lymphoma 52 0.039
478
P OVR049 Ovarian Disease 52 0.039
479
SPL004 Splenic Marginal Zone Lymphoma 51 0.039
480
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.039
481
SCH012 Schizoaffective Disorder 50 0.039
482
c PRM012 Primary Polycythemia 50 0.039
483
c INF145 Infantile Liver Failure Syndrome 1 50 0.039
484
PLC008 Placenta Disease 50 0.039
485
NTR046 Neutrophil Migration 50 0.039
486
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.039
487
ATY042 Atypical Chronic Myeloid Leukemia 49 0.039
488
c THR090 Thrombocythemia 1 49 0.039
489
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.039
490
P MST002 Mast-Cell Leukemia 49 0.039
491
MCR004 Macroglobulinemia 49 0.039
492
c FLL041 Follicular Lymphoma 1 49 0.039
493
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.039
494
INT054 Intraocular Lymphoma 48 0.039
495
CHR563 Chronic Eosinophilic Leukemia 48 0.039
496
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.039
497
PRL017 Prolymphocytic Leukemia 47 0.039
498
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.039
499
PLS025 Plasmablastic Lymphoma 47 0.039
500
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.039
501
LYM019 Lymphosarcoma 46 0.039
502
MYC005 Myocardial Stunning 46 0.039
503
P BNG032 Benign Mesothelioma 46 0.039
504
PRL008 Paralytic Ileus 45 0.039
505
LYM051 Lymphomatoid Granulomatosis 45 0.039
506
GRN017 Granulocytopenia 44 0.039
507
LTH001 Lethal Midline Granuloma 44 0.039
508
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.039
509
DPR002 Depersonalization Disorder 43 0.039
510
SPN369 Spinal Disease 43 0.039
511
BNM001 Bone Marrow Cancer 43 0.039
512
CHR286 Chronic Neutrophilic Leukemia 42 0.039
513
GST020 Gastric Antral Vascular Ectasia 41 0.039
514
LRG008 Large Granular Lymphocyte Leukemia 41 0.039
515
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.039
516
ALX002 Alexithymia 38 0.039
517
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.039
518
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.039
519
ABD010 Abdominal Wall Defect 36 0.039
520
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.039
521
ATX010 Ataxia Neuropathy Spectrum 34 0.039
522
c LKM005 Leukemia, T-Cell, Chronic 34 0.039
523
SPP003 Suppurative Periapical Periodontitis 34 0.039
524
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.039
525
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.039
526
ACT064 Acute Necrotizing Encephalitis 33 0.039
527
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.039
528
TMP019 Temporomandibular Joint Anomaly 28 0.039
529
CLS052 Classic Hairy Cell Leukemia 27 0.039
530
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.039
531
BLD137 Blood Group--Ahonen 16 0.039
532
ESP021 Esophageal Cancer 90 0.035
533
INS024 Insulin-Like Growth Factor I 79 0.035
534
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.035
535
BRN028 Brain Cancer 74 0.035
536
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.035
537
P HNT016 Huntington Disease 72 0.035
538
SKN019 Skin Melanoma 68 0.035
539
RCK004 Rickets 68 0.035
540
P LNG028 Long Qt Syndrome 66 0.035
541
P ATR011 Atrial Fibrillation 66 0.035
542
KHL003 Kohlschutter-Tonz Syndrome 65 0.035
543
SRC014 Sarcoma 65 0.035
544
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.035
545
OVR029 Ovarian Hyperstimulation Syndrome 64 0.035
546
CLF027 Cleft Palate, Isolated 64 0.035
547
c JVN010 Juvenile Rheumatoid Arthritis 64 0.035
548
ART002 Arts Syndrome 64 0.035
549
c DPH024 Diaphragmatic Hernia, Congenital 63 0.035
550
P EPL140 Epilepsy, Idiopathic Generalized 62 0.035
551
c BRN108 Branchiootic Syndrome 1 62 0.035
552
INT066 Interstitial Lung Disease 60 0.035
553
P CTR002 Cataract 60 0.035
554
P RBL001 Rubella 59 0.035
555
P MCR010 Microcephaly 59 0.035
556
P BND020 Bone Disease 59 0.035
557
THY029 Thyroid Carcinoma 59 0.035
558
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.035
559
P EHL001 Ehlers-Danlos Syndrome 58 0.035
560
IRN002 Iron Metabolism Disease 57 0.035
561
THR024 Thrombosis 57 0.035
562
TNS005 Tonsillitis 57 0.035
563
P ANG015 Angioedema 57 0.035
564
P ADL017 Adult T-Cell Leukemia 56 0.035
565
BCT022 Bacterial Infectious Disease 56 0.035
566
SPN041 Spinal Cord Disease 56 0.035
567
SFT003 Soft Tissue Sarcoma 56 0.035
568
SCH003 Schizophreniform Disorder 56 0.035
569
NRL004 Neuroleptic Malignant Syndrome 56 0.035
570
ORP003 Oropharynx Cancer 55 0.035
571
LMB062 Limb Ischemia 55 0.035
572
P PTT006 Pituitary Adenoma 55 0.035
573
HDR002 Hidradenitis Suppurativa 55 0.035
574
CRT017 Cartilage Disease 54 0.035
575
VLC001 Velocardiofacial Syndrome 54 0.035
576
PRS045 Prostatic Hypertrophy 53 0.035
577
GST009 Gastroschisis 53 0.035
578
P CNT005 Central Nervous System Lymphoma 53 0.035
579
SPN035 Spindle Cell Sarcoma 53 0.035
580
GST023 Gastric Ulcer 53 0.035
581
PRP080 Peripheral Artery Disease 53 0.035
582
ESP023 Esophageal Disease 52 0.035
583
OLG003 Oligohydramnios 51 0.035
584
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.035
585
PRS021 Prostatic Adenoma 51 0.035
586
LNG031 Lung Benign Neoplasm 51 0.035
587
ACT017 Acute Chest Syndrome 51 0.035
588
c ALM001 Al Amyloidosis 50 0.035
589
P OBS001 Obstructive Jaundice 50 0.035
590
PLP001 Pulpitis 49 0.035
591
HDR003 Hidradenitis 49 0.035
592
PRS129 Prostatic Hyperplasia, Benign 49 0.035
593
URM002 Uremia 49 0.035
594
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.035
595
P RNV001 Renovascular Hypertension 48 0.035
596
LPT006 Leptin Receptor Deficiency 48 0.035
597
c PRM226 Primary Central Nervous System Lymphoma 48 0.035
598
PLC007 Placental Abruption 48 0.035
599
CNT033 Central Nervous System Cancer 47 0.035
600
CRD137 Cardiogenic Shock 47 0.035
601
P OVR046 Ovarian Cyst 47 0.035
602
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.035
603
SMT001 Somatization Disorder 46 0.035
604
EXT010 Extramedullary Plasmacytoma 45 0.035
605
CYN002 Cyanosis, Transient Neonatal 45 0.035
606
c SPN097 Spinocerebellar Ataxia 23 45 0.035
607
IMP006 Impulse Control Disorder 45 0.035
608
MLN073 Melanosis, Neurocutaneous 45 0.035
609
ASP008 Aspiration Pneumonitis 45 0.035
611
DVR002 Diverticulitis 43 0.035
612
NSP002 Nasopharyngitis 43 0.035
613
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.035
614
DRG024 Drug Allergy 42 0.035
615
DBT002 Diabetic Autonomic Neuropathy 41 0.035
616
PHB003 Phobia, Specific 41 0.035
617
P MLG074 Malignant Mesenchymoma 40 0.035
618
HYP784 Hypogonadism, Male 40 0.035
619
ALG001 Algoneurodystrophy 39 0.035
620
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.035
621
c MJR008 Major Affective Disorder 2 35 0.035
622
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.035
623
c MJR023 Major Affective Disorder 7 33 0.035
624
RFR002 Refractory Hairy Cell Leukemia 33 0.035
625
c MJR003 Major Affective Disorder 6 33 0.035
626
c MJR006 Major Affective Disorder 5 33 0.035
627
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.035
628
HND015 Hand Skill, Relative 33 0.035
629
c MJR004 Major Affective Disorder 4 28 0.035
630
ARG004 Argyria 27 0.035
631
P RTT002 Rett Syndrome 80 0.030
632
CNN003 Conn's Syndrome 79 0.030
633
END057 Endometrial Cancer 74 0.030
634
MLT157 Multiple System Atrophy 1 70 0.030
635
c PNC108 Pancreatitis, Hereditary 70 0.030
636
P MYP004 Myopathy 70 0.030
637
P MCR115 Microvascular Complications of Diabetes 5 66 0.030
638
AND002 Androgen Insensitivity Syndrome 66 0.030
639
c FML001 Familial Atrial Fibrillation 65 0.030
640
PPL049 Papillon-Lefevre Syndrome 65 0.030
641
c DBT099 Diabetes Mellitus, Type I 65 0.030
642
P ADL010 Adult Respiratory Distress Syndrome 65 0.030
643
CLN015 Colon Adenocarcinoma 65 0.030
644
DGR001 Digeorge Syndrome 64 0.030
645
c PRC016 Pre-Eclampsia 63 0.030
646
TRN015 Transient Cerebral Ischemia 63 0.030
647
P PRM006 Primary Biliary Cirrhosis 62 0.030
648
P CHL002 Childhood Absence Epilepsy 61 0.030
649
P ENC004 Encephalitis 61 0.030
650
DCB001 Decubitus Ulcer 61 0.030
651
P AXN002 Axenfeld-Rieger Syndrome 59 0.030
652
BRS051 Breast Disease 58 0.030
653
ERY003 Erythema Multiforme 58 0.030
654
P CND004 Candidiasis 58 0.030
655
P MYS005 Myositis 56 0.030
656
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.030
657
NRG002 Neurogenic Bladder 55 0.030
658
P DYS193 Dystonia 11, Myoclonic 55 0.030
659
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.030
660
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.030
661
GLC003 Glucose Intolerance 54 0.030
662
P LTR001 Lateral Sclerosis 54 0.030
663
P INS002 in Situ Carcinoma 53 0.030
664
CRH005 Crohn's Colitis 53 0.030
665
BRN038 Bronchial Disease 53 0.030
666
P HMR003 Hemorrhagic Disease 53 0.030
667
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.030
668
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.030
669
ALC009 Alcoholic Liver Cirrhosis 53 0.030
670
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.030
671
DMY004 Demyelinating Disease 52 0.030
672
P RCT021 Rectum Cancer 52 0.030
673
c PNC106 Pancreatic Agenesis 1 51 0.030
674
NRM004 Neuroma 51 0.030
675
P HYP040 Hypospadias 51 0.030
676
BRX001 Bruxism 50 0.030
677
RTN003 Retinal Ischemia 50 0.030
678
MTB004 Metabolic Acidosis 50 0.030
679
GYN001 Gynecomastia 49 0.030
680
P MGR001 Migraine Without Aura 49 0.030
681
PNC034 Pancreas Disease 48 0.030
682
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.030
683
SPC010 Speech and Communication Disorders 47 0.030
684
LYM012 Lymphoplasmacytic Lymphoma 47 0.030
685
RTN023 Retinitis 46 0.030
686
SPN020 Spondylosis 46 0.030
687
P HMR005 Hemorrhoid 46 0.030
688
SVN002 Sveinsson Chorioretinal Atrophy 46 0.030
689
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.030
690
AGR002 Agoraphobia 45 0.030
691
IMM064 Immunodeficiency, Common Variable, 10 44 0.030
692
ACH015 Achalasia, Familial Esophageal 44 0.030
693
HPT082 Hepatic Adenomas, Familial 44 0.030
694
URT014 Ureterolithiasis 44 0.030
695
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.030
696
NRR001 Neuroretinitis 42 0.030
697
PHB001 Phobic Disorder 41 0.030
698
DYS011 Dyskinesia of Esophagus 41 0.030
699
PCD001 Pica Disease 41 0.030
700
ANG049 Angioedema Induced by Ace Inhibitors 40 0.030
701
SCH011 Schizotypal Personality Disorder 40 0.030
702
ADP007 Adie Pupil 39 0.030
703
c MLG157 Malignant Pheochromocytoma 38 0.030
704
ALG027 Al-Gazali-Bakalinova Syndrome 38 0.030
705
SPR012 Separation Anxiety Disorder 38 0.030
706
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.030
707
KLP001 Kleptomania 38 0.030
708
SWL001 Swallowing Disorders 38 0.030
709
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.030
710
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.030
711
THR123 Thrombotic Microangiopathy 36 0.030
712
ALR002 Al-Raqad Syndrome 33 0.030
713
INF021 Infant Gynecomastia 31 0.030
714
NRG001 Neurogenic Bowel 31 0.030
715
PST044 Postorgasmic Illness Syndrome 30 0.030
716
HNM002 Hinman Syndrome 27 0.030
717
HRP008 Herpes Simiae 25 0.030
718
c SYS001 Systemic Lupus Erythematosus 86 0.025
719
P ATX030 Ataxia-Telangiectasia 82 0.025
720
CYS001 Cystic Fibrosis 81 0.025
721
P GLM040 Glioma Susceptibility 1 81 0.025
722
c NRF023 Neurofibromatosis, Type Ii 80 0.025
723
c DLT002 Dilated Cardiomyopathy 79 0.025
724
P RTN008 Retinitis Pigmentosa 79 0.025
725
GST019 Gastrointestinal Stromal Tumor 78 0.025
726
P LNG064 Lung Cancer Susceptibility 3 78 0.025
727
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.025
728
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.025
729
P APL001 Aplastic Anemia 74 0.025
730
c HMC039 Hemochromatosis, Type 1 74 0.025
731
P RTN024 Retinoblastoma 73 0.025
732
P GRF003 Graft-Versus-Host Disease 72 0.025
733
OTT002 Otitis Media 72 0.025
734
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.025
735
SVR097 Severe Cutaneous Adverse Reaction 69 0.025
736
P ANG001 Angelman Syndrome 69 0.025
737
P MYC084 Mycobacterium Tuberculosis 1 68 0.025
738
c BSL007 Basal Cell Carcinoma 68 0.025
739
P INF038 Influenza 68 0.025
740
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.025
741
P THR014 Thrombocytopenia 67 0.025
742
CHR103 Charge Syndrome 67 0.025
743
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.025
744
c INF071 Inflammatory Bowel Disease 1 67 0.025
745
P MLG056 Malignant Hyperthermia 67 0.025
746
PRT010 Parathyroid Carcinoma 67 0.025
747
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.025
748
P SKN015 Skin Carcinoma 66 0.025
749
P NSP012 Nasopharyngeal Carcinoma 66 0.025
750
ART001 Arterial Tortuosity Syndrome 66 0.025
751
P MNN013 Meningitis 66 0.025
752
LNG039 Lung Squamous Cell Carcinoma 66 0.025
753
P PLM036 Pulmonary Fibrosis 65 0.025
754
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.025
755
KRT019 Keratitis, Hereditary 65 0.025
756
BRR014 Barrett Esophagus 65 0.025
757
PND002 Pendred Syndrome 65 0.025
758
ATH013 Atherosclerosis Susceptibility 65 0.025
759
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.025
760
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.025
761
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.025
762
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.025
763
P PRD008 Periodontitis 64 0.025
764
MSC007 Muscle Hypertrophy 64 0.025
765
PLM031 Poliomyelitis 64 0.025
766
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.025
767
LSH001 Leishmaniasis 63 0.025
768
P NTR004 Neutropenia 63 0.025
769
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.025
770
c MLG084 Malignant Fibrous Histiocytoma 63 0.025
771
P SHR029 Short Syndrome 63 0.025
772
INT146 Intervertebral Disc Disease 63 0.025
773
END041 Endometrial Adenocarcinoma 63 0.025
774
HYP780 Hypoadrenocorticism, Familial 63 0.025
775
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.025
776
P ACR001 Aicardi-Goutieres Syndrome 62 0.025
777
BLD131 Bladder Urothelial Carcinoma 62 0.025
778
MSL001 Measles 62 0.025
779
FTT001 Fatty Liver Disease 61 0.025
780
c SCL052 Scleroderma, Familial Progressive 61 0.025
781
RTN017 Retinal Detachment 61 0.025
782
P LPS004 Lupus Erythematosus 61 0.025
783
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 61 0.025
784
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.025
785
P VNT002 Ventricular Septal Defect 60 0.025
786
P ALP009 Alopecia Areata 60 0.025
787
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.025
788
P SNS001 Sensorineural Hearing Loss 60 0.025
789
CHC001 Chickenpox 60 0.025
790
STF001 Stiff-Person Syndrome 60 0.025
791
DYS164 Dyskeratosis Congenita, X-Linked 60 0.025
792
c ALB021 Albinism, Oculocutaneous, Type Ii 59 0.025
793
IDP011 Idiopathic Interstitial Pneumonia 59 0.025
794
CHL123 Chlamydia 59 0.025
795
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.025
796
IRN001 Iron Deficiency Anemia 59 0.025
797
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.025
798
GLB001 Gilbert Syndrome 58 0.025
799
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.025
800
P INT070 Intestinal Obstruction 58 0.025
801
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.025
802
NWB001 Newborn Respiratory Distress Syndrome 58 0.025
803
P MMP001 Mumps 58 0.025
804
P GLM007 Glomerulonephritis 57 0.025
805
BRN056 Bronchopulmonary Dysplasia 57 0.025
806
BRD001 Brody Myopathy 57 0.025
807
c ALZ056 Alzheimer Disease 3 57 0.025
808
CMM005 Common Cold 57 0.025
809
ARS001 Aarskog-Scott Syndrome 57 0.025
810
P FTL001 Fetal Alcohol Syndrome 57 0.025
811
VSC002 Vascular Dementia 57 0.025
812
LNN001 Lennox-Gastaut Syndrome 57 0.025
813
SCH014 Schistosomiasis 57 0.025
814
INT303 Intracranial Hypertension, Idiopathic 57 0.025
815
PHR003 Pharyngitis 57 0.025
816
CMR002 Coumarin Resistance 56 0.025
817
P MLT074 Multiple Endocrine Neoplasia 56 0.025
818
ADN027 Adenomyosis 56 0.025
819
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.025
820
ALL010 Allergic Contact Dermatitis 56 0.025
821
MTH009 Mouth Disease 56 0.025
822
HMG005 Hemoglobinopathy 56 0.025
823
SML019 Smallpox 56 0.025
824
P GST044 Gastritis 56 0.025
825
c FML035 Familial Hyperlipidemia 55 0.025
826
HYP005 Hypokalemia 55 0.025
827
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.025
828
ACT058 Active Peptic Ulcer Disease 55 0.025
829
CRC006 Carcinoid Syndrome 55 0.025
830
P ALP106 Alport Syndrome 1, X-Linked 55 0.025
831
P FNG006 Feingold Syndrome 1 55 0.025
832
URN010 Urinary Tract Obstruction 55 0.025
833
INT007 Intermediate Coronary Syndrome 55 0.025
834
SMT008 Smith-Magenis Syndrome 54 0.025
835
SCH071 Schaaf-Yang Syndrome 54 0.025
836
P ART021 Arteriosclerosis 54 0.025
837
PPL022 Papilloma 54 0.025
838
SLP001 Sleeping Sickness 54 0.025
839
NNL006 Non-Alcoholic Steatohepatitis 54 0.025
840
FRZ001 Frozen Shoulder 53 0.025
841
P EPD016 Epidermolysis Bullosa 53 0.025
842
c PRD040 Periodontitis, Chronic 53 0.025
843
P ORL007 Oral Cavity Cancer 53 0.025
844
GTR002 Goiter 53 0.025
845
c FML008 Familial Retinoblastoma 53 0.025
846
c CNT035 Central Nervous System Disease 52 0.025
847
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 0.025
848
P SML001 Small Cell Carcinoma 52 0.025
849
NRT004 Neuritis 52 0.025
850
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.025
851
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.025
852
THY030 Thyroid Gland Disease 52 0.025
853
P THY032 Thyroiditis 52 0.025
854
FML037 Female Breast Cancer 52 0.025
855
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 52 0.025
856
P MGR003 Migraine with Aura 52 0.025
857
INV006 Inverted Papilloma 52 0.025
858
TRC010 Trichotillomania 51 0.025
859
KRT009 Keratosis 51 0.025
860
THR016 Thrombophlebitis 51 0.025
861
ACT049 Acute Disseminated Encephalomyelitis 51 0.025
862
TNG007 Tongue Carcinoma 51 0.025
863
BHR001 Behr Syndrome 51 0.025
864
HYP781 Hypoascorbemia 51 0.025
865
PTT041 Pituitary Stalk Interruption Syndrome 50 0.025
866
PLR007 Pleural Empyema 50 0.025
867
P ECL001 Eclampsia 50 0.025
868
BRN009 Burning Mouth Syndrome 50 0.025
869
CRT013 Carotid Stenosis 50 0.025
870
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 50 0.025
871
ALN001 Aland Island Eye Disease 50 0.025
872
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.025
873
ART017 Aortic Disease 49 0.025
874
c TRC091 Trichorhinophalangeal Syndrome, Type Ii 49 0.025
875
CHL004 Cholelithiasis 49 0.025
876
c SPN330 Spondylocostal Dysostosis 5 49 0.025
877
DNT045 Dental Anomalies and Short Stature 49 0.025
878
QDR001 Quadriplegia 48 0.025
879
c BCT013 Bacterial Pneumonia 48 0.025
880
BNR002 Bone Resorption Disease 48 0.025
881
BRS064 Bursitis 48 0.025
882
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.025
883
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.025
884
SPL018 Splenomegaly 48 0.025
885
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.025
886
P HRD021 Hereditary Sensory Neuropathy 48 0.025
887
P DPY001 Dupuytren Contracture 48 0.025
888
PRP007 Priapism 47 0.025
889
CRD001 Cardiac Tamponade 47 0.025
890
KRT008 Keratopathy 47 0.025
891
NRN001 Neuroendocrine Carcinoma 47 0.025
892
P CLL015 Collagen Disease 47 0.025
893
KRT002 Keratomalacia 47 0.025
894
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.025
895
CYC008 Cyclic Vomiting Syndrome 47 0.025
896
c PRM093 Premature Ovarian Failure 7 47 0.025
897
P PRC019 Precocious Puberty 46 0.025
898
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.025
899
RTN020 Retinal Vascular Disease 46 0.025
900
P ANX007 Anauxetic Dysplasia 1 46 0.025
901
c ALP104 Alport Syndrome 3, Autosomal Dominant 46 0.025
902
CLN045 Colonic Benign Neoplasm 46 0.025
903
EXS001 Exostosis 46 0.025
904
STT007 Steatocystoma Multiplex 46 0.025
905
HYD005 Hydrocele 46 0.025
906
P MTH007 Methemoglobinemia 46 0.025
907
OBS003 Obsessive-Compulsive Personality Disorder 46 0.025
908
SQM002 Squamous Cell Papilloma 46 0.025
909
P HRN001 Horner's Syndrome 45 0.025
910
RTR008 Root Resorption 45 0.025
911
SPS007 Spastic Cerebral Palsy 45 0.025
912
ATN004 Autonomic Neuropathy 45 0.025
913
CNT017 Central Nervous System Origin Vertigo 45 0.025
914
c DRM054 Dermatitis, Atopic, 2 44 0.025
915
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 0.025
916
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.025
917
TNG009 Tongue Squamous Cell Carcinoma 44 0.025
918
PPL001 Papillary Adenoma 44 0.025
919
P BCT020 Bacteremia 2 44 0.025
920
EMP001 Empty Sella Syndrome 44 0.025
921
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.025
922
MRG013 Mirage Syndrome 43 0.025
923
URT037 Urethral Stricture 43 0.025
924
MGS001 Megaesophagus 43 0.025
925
MDD018 Middle East Respiratory Syndrome 43 0.025
926
ORL015 Oral Squamous Cell Carcinoma 43 0.025
927
P HYP265 Hypotonia 43 0.025
928
VRL003 Variola Major 42 0.025
929
HYP457 Hypertrophic Scars 42 0.025
930
BNS003 Binswanger's Disease 42 0.025
931
P AVS003 Avascular Necrosis 42 0.025
932
PHY002 Physical Disorder 42 0.025
933
P PRT026 Parotitis 42 0.025
934
EXC002 Exocrine Pancreatic Insufficiency 42 0.025
935
GLC096 Galactorrhea 42 0.025
936
c RTN041 Retinitis Pigmentosa 11 42 0.025
937
P KLZ004 Kala-Azar 1 41 0.025
938
RST023 Resting Heart Rate, Variation in 41 0.025
939
BDY001 Body Dysmorphic Disorder 40 0.025
940
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.025
941
CYC005 Cyclothymic Disorder 40 0.025
942
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.025
943
C1N001 C1 Inhibitor Deficiency 39 0.025
944
P STR001 Striatonigral Degeneration 39 0.025
945
c HYP507 Hypotrichosis 1 39 0.025
946
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.025
947
FML039 Female Reproductive System Disease 39 0.025
948
NM001 Noma 38 0.025
949
c PLY105 Polycystic Ovary Syndrome 1 38 0.025
950
OVR094 Ovarian Epithelial Cancer 38 0.025
951
CHL073 Cholestasis-Lymphedema Syndrome 38 0.025
952
SPS019 Spastic Paraparesis 38 0.025
953
BLR004 Biliary Dyskinesia 38 0.025
954
CRB009 Cerebritis 37 0.025
955
P CRB088 Cerebral Atrophy 37 0.025
956
GLM044 Glomerular Disease 37 0.025
957
c PRG021 Paragangliomas 4 37 0.025
958
SPN331 Spondyloocular Syndrome 36 0.025
959
TRG003 Trigeminal Nerve Disease 36 0.025
960
HYP137 Hypotrichosis Simplex 35 0.025
961
ACL001 Acalculous Cholecystitis 35 0.025
962
c MCR312 Microphthalmia, Syndromic 10 35 0.025
963
BRK012 Broken Heart Syndrome 35 0.025
964
RTR010 Retroperitoneal Sarcoma 34 0.025
965
c RST012 Restless Legs Syndrome 1 34 0.025
966
c SBC003 Subacute Bacterial Endocarditis 33 0.025
967
DRG001 Drug Psychosis 33 0.025
968
MCR119 Microtia, Hearing Impairment, and Cleft Palate 33 0.025
969
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.025
970
c BLD140 Blood Group, I System 32 0.025
971
FMR018 Femoral-Facial Syndrome 32 0.025
972
TRG019 Trigonocephaly with Short Stature and Developmental Delay 32 0.025
973
PST103 Postpartum Psychosis 32 0.025
974
NRN002 Neuronitis 32 0.025
975
SBS005 Substance-Induced Psychosis 31 0.025
976
SPC003 Specific Developmental Disorder 31 0.025
977
DFF031 Diffuse Alveolar Hemorrhage 30 0.025
978
ERY066 Erythema Multiforme Major 30 0.025
979
FNT004 Fainting 30 0.025
980
SPN392 Spondylosis, Cervical 30 0.025
981
RSP007 Respiratory Distress Syndrome, Infant 30 0.025
982
CLF051 Cleft Larynx, Posterior 30 0.025
983
MYC088 Mycobacterium Avium Complex Infections 29 0.025
984
BRN008 Brain Compression 29 0.025
985
c DRR018 Diarrhea 9 28 0.025
986
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.025
987
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.025
988
CGN007 Cognitive Function 1, Social 27 0.025
989
LRY026 Laryngeal Cleft 27 0.025
990
PGM030 Pigmentation Anomaly of the Skin 26 0.025
991
ETH012 Ethylene Glycol Poisoning 26 0.025
992
c ATS371 Autism 6 25 0.025
993
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.025
994
OCC008 Occipital Neuralgia 25 0.025
995
CRR012 Cirrhotic Cardiomyopathy 24 0.025
996
OGL001 Ogilvie Syndrome 24 0.025
997
DRG004 Drug-Induced Mental Disorder 24 0.025
998
BLD163 Blood Group, Dombrock System 24 0.025
999
APN006 Apnea of Prematurity 24 0.025
1000
NCR014 Necrotizing Soft Tissue Infection 23 0.025
1001
CHR158 Charles Bonnet Syndrome 23 0.025
1002
MNC020 Monoclonal Mast Cell Activation Syndrome 22 0.025
1003
CRN234 Craniosynostosis, Adelaide Type 21 0.025
1004
BLD165 Blood Group, Colton System 20 0.025
1005
AND005 Androgen Insensitivity Syndrome, Mild 19 0.025
1006
JCK003 Jackhammer Esophagus 17 0.025
1007
MDL024 Madelung Deformity 17 0.025
1008
NVL002 Novelty Seeking Personality Trait 16 0.025
1009
P EST010 Esterase B 14 0.025
1010
c FNC027 Fanconi Anemia, Complementation Group a 81 0.018
1011
MLR004 Malaria 81 0.018
1012
P MDL005 Medulloblastoma 77 0.018
1013
c NRF024 Neurofibromatosis, Type I 77 0.018
1014
c MNN043 Meningioma, Familial 74 0.018
1015
c HYP836 Hypercholesterolemia, Familial, 1 73 0.018
1016
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.018
1017
ACR007 Acromegaly 71 0.018
1018
c EXD008 Exudative Vitreoretinopathy 1 71 0.018
1019
P SRC025 Sarcoidosis 1 70 0.018
1020
ADN011 Adenoid Cystic Carcinoma 70 0.018
1021
P TTR001 Tetralogy of Fallot 70 0.018
1022
PLM001 Pulmonary Tuberculosis 69 0.018
1023
ACR008 Acrocallosal Syndrome 69 0.018
1024
P LPR021 Leprosy 3 69 0.018
1025
EWN003 Ewing Sarcoma 69 0.018
1026
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.018
1027
P CRN037 Craniosynostosis 68 0.018
1028
P TMP003 Temporal Arteritis 68 0.018
1029
CHL065 Cholangiocarcinoma 68 0.018
1030
SND001 Sandhoff Disease 68 0.018
1031
CMM004 Common Variable Immunodeficiency 68 0.018
1032
P MYS003 Myasthenia Gravis 68 0.018
1033
CNN005 Connective Tissue Disease 68 0.018
1034
P FRN006 Frontotemporal Dementia 68 0.018
1035
FCT007 Factor Vii Deficiency 67 0.018
1036
P OLG002 Oligodendroglioma 67 0.018
1037
c HMP029 Hemophilia a 67 0.018
1038
P SHW006 Shwachman-Diamond Syndrome 1 67 0.018
1039
FLL027 Fallopian Tube Carcinoma 67 0.018
1040
P BLD062 Bile Duct Cancer 67 0.018
1041
CHD001 Chediak-Higashi Syndrome 66 0.018
1042
P MSC005 Muscular Dystrophy 66 0.018
1043
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.018
1044
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.018
1045
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.018
1046
CRN036 Craniopharyngioma 65 0.018
1047
P ART005 Arteriovenous Malformation 65 0.018
1048
P CNJ013 Conjunctivitis 65 0.018
1049
DMN031 Dementia, Lewy Body 65 0.018
1050
P MTR014 Motor Neuron Disease 65 0.018
1051
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.018
1052
c ART101 Aortic Valve Disease 2 65 0.018
1053
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.018
1054
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.018
1055
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.018
1056
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.018
1057
P FRD001 Friedreich Ataxia 64 0.018
1058
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.018
1059
P PLZ001 Pelizaeus-Merzbacher Disease 64 0.018
1060
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.018
1061
DSM004 Desmoid Tumor 64 0.018
1062
KND001 Kindler Syndrome 64 0.018
1063
LYM017 Lyme Disease 64 0.018
1064
c EPS035 Episodic Ataxia, Type 2 63 0.018
1065
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.018
1066
P HML002 Hemolytic Anemia 63 0.018
1067
P HYP069 Hyperparathyroidism 63 0.018
1068
P THR117 Three M Syndrome 1 63 0.018
1069
P HYP055 Hypoplastic Left Heart Syndrome 63 0.018
1070
CHN016 Cohen Syndrome 63 0.018
1071
P LMY004 Leiomyosarcoma 63 0.018
1072
RHB001 Rhabdoid Cancer 63 0.018
1073
c ATM011 Autoimmune Hepatitis 63 0.018
1074
c OPT053 Optic Atrophy 1 63 0.018
1075
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.018
1076
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.018
1077
HMT002 Hematologic Cancer 62 0.018
1078
P PLY014 Polycystic Kidney Disease 62 0.018
1079
c GLY004 Glycogen Storage Disease V 62 0.018
1080
P SPN046 Spinal Muscular Atrophy 62 0.018
1081
LSC001 Lesch-Nyhan Syndrome 62 0.018
1082
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 0.018
1083
BRS099 Breast Ductal Carcinoma 62 0.018
1084
MNN042 Meningioma, Radiation-Induced 62 0.018
1085
P OST009 Osteochondritis Dissecans 62 0.018
1086