Search results for Gabapentin

1118 hits were found for Gabapentin

# Family MCID Name MIFTS Score
1
PST053 Postherpetic Neuralgia 40 10.912
2
DBT010 Diabetic Neuropathy 54 10.191
3
P CHR345 Chronic Pain 50 10.019
4
P SZR006 Seizure Disorder 69 9.832
5
P RST001 Restless Legs Syndrome 52 9.224
6
PNG002 Pain Agnosia 51 8.748
7
P NRP001 Neuropathy 59 8.529
8
c PNS012 Paine Syndrome 60 8.471
9
FCL014 Focal Epilepsy 53 8.026
10
P PRP019 Peripheral Nervous System Disease 57 7.328
11
c EPS039 Episodic Pain Syndrome, Familial, 1 42 7.219
12
ALC007 Alcohol Dependence 65 6.961
13
P ALC033 Alcohol Use Disorder 67 6.756
14
P EPL164 Epilepsy 70 6.722
15
c MJR024 Major Affective Disorder 9 40 6.518
16
c MJR022 Major Affective Disorder 8 37 6.518
17
P BPL003 Bipolar Disorder 56 6.518
18
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 6.136
19
P TRM003 Tremor 50 6.093
20
P HDC001 Headache 56 5.994
21
ANX010 Anxiety 70 5.632
22
FBR047 Fibromyalgia 58 5.494
23
PTH003 Pathologic Nystagmus 52 5.487
24
DBT002 Diabetic Autonomic Neuropathy 40 5.020
25
HRP004 Herpes Zoster 60 4.938
26
WTH001 Withdrawal Disorder 47 4.936
27
SPN186 Spinal Cord Injury 61 4.836
28
P SBS003 Substance Abuse 54 4.686
29
URM005 Uremic Pruritus 45 4.667
30
P PRK057 Parkinson Disease, Late-Onset 79 4.636
31
RFL001 Reflex Sympathetic Dystrophy 51 4.586
32
ALG001 Algoneurodystrophy 37 4.586
33
CMP010 Complex Regional Pain Syndrome 59 4.493
34
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.407
35
P CRP001 Carpal Tunnel Syndrome 66 4.296
36
SBC016 Subacute Delirium 42 4.128
37
END086 End Stage Renal Disease 54 4.108
38
OPT003 Opiate Dependence 49 4.082
39
P PLY019 Polyneuropathy 53 3.897
40
BCK006 Back Pain 43 3.849
41
MNT002 Mental Depression 56 3.806
42
ANT039 Antisynthetase Syndrome 55 3.795
43
TRG002 Trigeminal Neuralgia 61 3.726
44
RDC002 Radiculopathy 51 3.688
45
P ANR048 Aniridia 1 66 3.687
46
P MYC033 Myoclonus 46 3.686
47
DPR016 Depression 65 3.670
48
CCN001 Cocaine Dependence 48 3.626
49
MDD011 Mood Disorder 62 3.604
50
ALL029 Allergic Disease 61 3.545
51
c MGR028 Migraine with or Without Aura 1 64 3.539
52
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 3.524
53
c CHR684 Chronic Kidney Disease 74 3.465
54
P MCR129 Microvascular Complications of Diabetes 1 68 3.449
55
OPD001 Opioid Abuse 44 3.419
56
OST012 Osteoarthritis 77 3.419
57
MCS002 Mucositis 55 3.405
58
P EXN002 Exanthem 58 3.385
59
SPN027 Spinal Stenosis 59 3.359
60
P BRS047 Breast Cancer 97 3.331
61
P SCL018 Scoliosis 57 3.285
62
48X005 48,xyyy 39 3.270
63
CNS004 Constipation 56 3.262
64
P TRN020 Turner Syndrome 67 3.183
65
c RST012 Restless Legs Syndrome 1 33 3.156
66
PRS063 Paresthesia 39 3.112
67
P INT143 Interstitial Cystitis 59 3.109
68
SQM013 Squamous Cell Carcinoma, Head and Neck 75 3.106
69
ING001 Inguinal Hernia 59 3.097
70
P MLT020 Multiple Sclerosis 79 3.077
71
CNN001 Cannabis Dependence 38 3.065
72
P KDN018 Kidney Disease 72 2.990
73
SPS057 Spasticity 43 2.897
74
RHB024 Rhabdomyosarcoma 2 65 2.880
75
IDP070 Idiopathic Scoliosis 41 2.838
76
PST028 Post-Traumatic Stress Disorder 59 2.807
77
EPT021 Epithelial Recurrent Erosion Dystrophy 46 2.765
78
LWC001 Low Compliance Bladder 44 2.738
79
LPT014 Leptin Deficiency or Dysfunction 77 2.736
80
AGN016 Aging 54 2.700
81
P NRV007 Nervous System Disease 66 2.689
82
VSL002 Visual Epilepsy 39 2.678
83
AND005 Androgen Insensitivity Syndrome, Mild 21 2.678
84
PSY004 Psychotic Disorder 66 2.630
85
DBT004 Diabetic Polyneuropathy 50 2.626
86
PRS047 Prostatitis 58 2.619
87
P CTR002 Cataract 59 2.607
88
P LTR001 Lateral Sclerosis 58 2.557
89
P MVM001 Movement Disease 61 2.551
90
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 39 2.550
91
c ESS001 Essential Tremor 56 2.518
92
P PRK039 Parkinsonism 55 2.512
93
OPD006 Opioid Addiction 48 2.492
94
SQM006 Squamous Cell Carcinoma 59 2.484
95
MNN028 Mononeuropathy of the Median Nerve, Mild 46 2.480
96
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.468
97
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 2.458
98
c BPL002 Bipolar I Disorder 47 2.449
99
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.446
100
P RSP003 Respiratory Failure 74 2.442
101
STT001 Status Epilepticus 58 2.415
102
P ART022 Arthritis 70 2.396
103
P DMN002 Dementia 65 2.381
104
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.359
105
DSS008 Disease of Mental Health 74 2.345
106
P VSC007 Vascular Disease 62 2.321
107
LVR012 Liver Cirrhosis 62 2.314
108
PLY068 Polysubstance Abuse 41 2.281
109
DWN001 Down Syndrome 70 2.275
110
P PNC044 Pancreatitis 61 2.239
111
INT146 Intervertebral Disc Disease 61 2.215
112
CHL068 Cholestasis 61 2.197
113
ORP003 Oropharynx Cancer 54 2.189
114
P DYS154 Dystonia 64 2.184
115
DRG003 Drug Dependence 46 2.160
116
P CYS018 Cystitis 59 2.143
117
BRX001 Bruxism 51 2.131
118
P ALP008 Alopecia 53 2.131
119
ADL002 Adult Syndrome 69 2.086
120
P LVR013 Liver Disease 68 2.068
121
P STR020 Strabismus 56 2.057
122
MCH006 Mechanical Strabismus 40 2.057
123
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.054
124
SNS003 Sensory Peripheral Neuropathy 51 2.042
125
CCN002 Cocaine Abuse 49 2.017
126
P PRS040 Prostate Cancer 95 2.008
127
IRR002 Irritable Bowel Syndrome 65 1.993
128
GNR004 Generalized Anxiety Disorder 55 1.992
129
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.974
130
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 1.974
131
PRM050 Primary Orthostatic Tremor 24 1.970
132
c TYP009 Type 2 Diabetes Mellitus 92 1.936
133
SMT001 Somatization Disorder 50 1.933
134
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.931
135
PNF002 Painful Legs and Moving Toes Syndrome 14 1.922
136
P AST005 Asthma 76 1.917
137
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.914
138
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.914
139
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.914
140
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.914
141
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.914
142
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.914
143
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.914
144
OST062 Osteoarthritis with Mild Chondrodysplasia 47 1.914
145
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.914
146
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.914
147
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.914
148
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.914
149
MYF002 Myofascial Pain Syndrome 46 1.914
150
CMP006 Complex Partial Epilepsy 36 1.896
151
P GLL022 Guillain-Barre Syndrome 59 1.893
152
P SLP006 Sleep Apnea 69 1.853
153
P PRP029 Porphyria 60 1.840
154
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.827
155
AYM001 Ayme-Gripp Syndrome 57 1.812
156
LPT006 Leptin Receptor Deficiency 50 1.812
157
ACT011 Acute Contagious Conjunctivitis 42 1.812
158
P CNJ013 Conjunctivitis 66 1.812
159
ENT001 Enterocele 42 1.812
160
SPN033 Spontaneous Ocular Nystagmus 25 1.812
161
CNN002 Cannabis Abuse 44 1.812
162
ILS001 Ileus 49 1.808
163
CRH001 Crohn's Disease 80 1.788
164
P ALZ034 Alzheimer Disease 87 1.782
165
TXC002 Toxic Encephalopathy 51 1.774
166
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 1.769
167
P SCK005 Sickle Cell Disease 56 1.767
168
GST092 Gastroesophageal Reflux 60 1.760
169
GLM045 Glioma 62 1.753
170
GLL048 Glial Tumor 52 1.753
171
CRB039 Cerebrovascular Disease 65 1.745
172
P SCL057 Scoliosis, Isolated 1 40 1.732
173
CHC001 Chickenpox 56 1.726
174
OCL069 Ocular Motor Apraxia 57 1.724
175
P SCH015 Schizophrenia 74 1.715
176
LNN001 Lennox-Gastaut Syndrome 61 1.710
177
SCL003 Social Phobia 48 1.708
178
P PRS038 Personality Disorder 65 1.705
179
STR067 Stroke, Ischemic 79 1.702
180
P PNC025 Panic Disorder 52 1.689
181
P SLP005 Sleep Disorder 62 1.688
182
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.680
183
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 1.670
184
P ATT013 Attention Deficit-Hyperactivity Disorder 66 1.665
185
P MYP004 Myopathy 67 1.665
186
CRB037 Cerebral Palsy 67 1.661
187
P PLM037 Pulmonary Hypertension 69 1.651
188
P ENC018 Encephalopathy 62 1.649
189
P BLD134 Bladder Cancer 79 1.647
190
P PLV020 Pelvic Organ Prolapse 58 1.647
191
P KDN017 Kidney Cancer 60 1.647
192
P TMP001 Temporal Lobe Epilepsy 49 1.642
193
OBS002 Obsessive-Compulsive Disorder 68 1.640
194
TRM010 Traumatic Brain Injury 50 1.640
195
PRP083 Porphyria, Acute Intermittent 64 1.636
196
P CLS010 Cluster Headache 42 1.624
197
SNC001 Sunct Headache 28 1.624
198
BRN071 Brain Injury 50 1.599
199
ATX019 Ataxia with Vitamin E Deficiency 44 1.589
200
FBR012 Fabry Disease 71 1.575
201
RFR003 Refractive Error 41 1.571
202
P GLM040 Glioma Susceptibility 1 70 1.566
203
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.561
204
P MJR001 Major Depressive Disorder 68 1.561
205
CHR073 Choreatic Disease 53 1.561
206
c ACT071 Acute Kidney Failure 60 1.561
207
P HMR005 Hemorrhoid 49 1.558
208
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.549
209
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.549
210
AMD002 Amed Syndrome, Digenic 37 1.549
211
c PRS130 Prostate Cancer, Hereditary, 8 32 1.549
212
c PRS136 Prostate Cancer, Hereditary, 6 33 1.549
213
c PNC108 Pancreatitis, Hereditary 68 1.549
214
CSY001 C Syndrome 61 1.549
215
RNL018 Renal Pelvis Carcinoma 29 1.549
216
SCH003 Schizophreniform Disorder 54 1.549
217
HNT002 Hantavirus Pulmonary Syndrome 55 1.549
218
P ERY008 Erythromelalgia 50 1.532
219
NRP027 Neuropathy, Painful 21 1.531
220
SXL003 Sexual Disorder 49 1.504
221
GLB002 Glioblastoma 67 1.504
222
SCH012 Schizoaffective Disorder 49 1.496
223
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.487
224
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.487
225
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.487
226
P MYS003 Myasthenia Gravis 68 1.479
227
P PRV006 Pervasive Developmental Disorder 52 1.473
228
URT037 Urethral Stricture 42 1.473
229
P MJR007 Major Affective Disorder 1 42 1.437
230
HMF011 Hemifacial Spasm, Familial 33 1.431
231
P HMF004 Hemifacial Spasm 38 1.431
232
c SZR022 Seizures, Benign Familial Neonatal, 1 42 1.431
233
CHR281 Chronic Hiccups 28 1.431
234
SMT006 Somatoform Disorder 50 1.429
235
SYN007 Synovitis 54 1.429
236
END040 Endogenous Depression 54 1.429
237
PLC002 Plica Syndrome 35 1.429
238
P HRT032 Heart Disease 84 1.391
239
ACT181 Acute Motor Axonal Neuropathy 25 1.390
240
HYP056 Hypoglycemia 65 1.379
241
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 1.379
242
PRT037 Pertussis 49 1.379
243
NSP002 Nasopharyngitis 45 1.371
244
P RCT021 Rectum Cancer 54 1.371
245
GLS004 Glossopharyngeal Neuralgia 37 1.368
246
BHR001 Behr Syndrome 50 1.365
247
CRB009 Cerebritis 43 1.365
248
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.345
249
P HNT016 Huntington Disease 73 1.345
250
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.339
251
RTN003 Retinal Ischemia 48 1.333
252
PST048 Postural Orthostatic Tachycardia Syndrome 46 1.305
253
P HPT021 Hepatitis 68 1.305
254
DYS073 Dysphagia 53 1.280
255
c MJR008 Major Affective Disorder 2 34 1.267
256
c MJR006 Major Affective Disorder 5 32 1.267
257
c MJR003 Major Affective Disorder 6 32 1.267
258
c MJR004 Major Affective Disorder 4 28 1.267
259
c MJR023 Major Affective Disorder 7 33 1.267
260
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.253
261
P HYP098 Hypereosinophilic Syndrome 66 1.253
262
NTL003 Notalgia Paresthetica 18 1.251
263
P MYS005 Myositis 56 1.242
264
BRN009 Burning Mouth Syndrome 51 1.231
265
P CNG024 Congenital Nystagmus 35 1.219
266
LRN003 Learning Disability 49 1.219
267
CRB004 Cerebral Artery Occlusion 46 1.207
268
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.206
269
ACR008 Acrocallosal Syndrome 70 1.206
270
P GST053 Gastric Cancer 82 1.206
271
BRD001 Brody Myopathy 54 1.206
272
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 1.206
273
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.206
274
TNS005 Tonsillitis 57 1.206
275
P LNG032 Lung Cancer 98 1.206
276
P INT260 Intracranial Berry Aneurysm 39 1.206
277
c BLD140 Blood Group, I System 47 1.206
278
NLP001 Nail-Patella Syndrome 63 1.206
279
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 1.206
280
GLS018 Glass Syndrome 60 1.206
281
KRT002 Keratomalacia 54 1.206
282
ANS011 Anus Cancer 55 1.206
283
AZS001 Azoospermia 45 1.206
284
PNL012 Penile Cancer 57 1.206
285
P NRV006 Nervous System Cancer 47 1.206
286
ANR040 Aneurysm 60 1.206
287
ANS025 Anus Benign Neoplasm 28 1.206
288
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.206
289
P ALP009 Alopecia Areata 59 1.206
290
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.206
291
TRD006 Tardive Dyskinesia 53 1.195
292
VSC002 Vascular Dementia 59 1.195
293
NNT008 Neonatal Abstinence Syndrome 40 1.194
294
SKN016 Skin Disease 62 1.182
295
BRN056 Bronchopulmonary Dysplasia 57 1.175
296
P CNR004 Cone-Rod Dystrophy 2 75 1.169
297
c ACT027 Acute Pancreatitis 60 1.169
298
P PNC035 Pancreatic Cancer 86 1.169
299
P VSC011 Vasculitis 61 1.168
300
OST159 Osteogenic Sarcoma 66 1.166
301
P URN019 Urinary Tract Infection 49 1.160
302
IMP005 Impotence 52 1.156
303
PRP016 Paraplegia 52 1.154
304
CNG034 Congestive Heart Failure 69 1.141
305
MRL006 Meralgia Paraesthetica, Familial 27 1.132
306
ADG002 Audiogenic Seizures 25 1.126
307
SRT004 Serotonin Syndrome 54 1.125
308
P LKM062 Leukemia, Acute Lymphoblastic 69 1.117
309
SYN036 Syncope 44 1.109
310
c HYP595 Hypertension, Essential 84 1.107
311
MNN017 Mononeuropathy 41 1.104
312
P MTR014 Motor Neuron Disease 65 1.104
313
NRT004 Neuritis 53 1.093
314
AMN003 Amnestic Disorder 54 1.093
315
PRP007 Priapism 46 1.092
316
RDN001 Reading Disorder 40 1.090
317
ACT084 Acute Stress Disorder 53 1.082
318
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 1.082
319
AMP007 Amphetamine Abuse 36 1.045
320
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.045
321
P MSC003 Muscular Atrophy 52 1.045
322
HYP266 Hypoxia 56 1.045
323
SBS004 Substance Dependence 46 1.045
324
IRN002 Iron Metabolism Disease 56 1.043
325
GLS013 Glossodynia 16 1.034
326
P SPN046 Spinal Muscular Atrophy 62 1.032
327
CYT002 Cytokine Deficiency 43 1.032
328
c SPN309 Spinocerebellar Ataxia 6 58 1.019
329
QDR001 Quadriplegia 49 1.019
330
DYS009 Dysthymic Disorder 51 1.019
331
P EPS003 Episodic Ataxia 59 1.019
332
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.019
333
P THR014 Thrombocytopenia 66 1.005
335
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.003
336
CHL004 Cholelithiasis 48 0.982
337
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.975
338
ANR004 Anuria 44 0.975
339
IFP003 Ifap Syndrome 2 42 0.959
340
NRM004 Neuroma 49 0.959
341
P KRT007 Keratoconus 50 0.959
342
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.959
343
P OLV001 Olivopontocerebellar Atrophy 51 0.942
344
PST011 Pustulosis of Palm and Sole 52 0.942
345
PRR013 Prurigo Nodularis 37 0.942
346
P PSR002 Psoriasis 63 0.942
347
HMC012 Hemicrania Continua 26 0.942
348
c ATS007 Autism Spectrum Disorder 72 0.933
349
NRT001 Neurotic Disorder 56 0.933
350
PRX035 Paroxysmal Dyskinesia 30 0.925
351
ART140 Arteries, Anomalies of 52 0.921
352
LPP008 Lipoprotein Quantitative Trait Locus 65 0.921
353
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.921
354
HYP458 Hyper Ige Syndrome 60 0.921
355
P KHL003 Kohlschutter-Tonz Syndrome 57 0.921
356
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.921
357
P CRN300 Coronary Heart Disease 1 73 0.921
358
ERY003 Erythema Multiforme 56 0.920
359
ERL001 Early Myoclonic Encephalopathy 63 0.920
360
CND002 Conduct Disorder 50 0.905
361
GTR002 Goiter 52 0.905
362
LCK001 Locked-in Syndrome 44 0.905
363
P EYD002 Eye Disease 57 0.905
364
TND005 Tendinitis 54 0.901
365
SVR097 Severe Cutaneous Adverse Reaction 68 0.898
366
PRD002 Periodic Limb Movement Disorder 33 0.898
367
47X002 47,xyy 48 0.898
368
ERY066 Erythema Multiforme Major 29 0.898
369
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.898
370
FNT004 Fainting 29 0.884
371
OPS006 Opsoclonus-Myoclonus Syndrome 48 0.884
372
INT395 Intracranial Meningioma 48 0.861
373
MNN043 Meningioma, Familial 79 0.861
374
DRM006 Dermatitis 62 0.861
375
PST047 Post-Traumatic Epilepsy 20 0.861
376
SCR001 Secretory Meningioma 40 0.861
377
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.861
378
TND004 Tendinopathy 45 0.861
379
P LYM118 Lymphoma 69 0.861
380
P CLR023 Colorectal Cancer 100 0.861
381
P ATS364 Autism 72 0.861
382
DFC004 Deficiency Anemia 74 0.861
383
P LKM002 Leukemia 66 0.861
384
P AGN002 Agnosia 53 0.861
385
TRL002 Tarlov Cysts 34 0.861
386
TLN003 Telangiectasis 51 0.851
387
P ATX030 Ataxia-Telangiectasia 80 0.838
388
P HRP006 Herpes Simplex 65 0.838
389
ERY029 Erythermalgia, Primary 58 0.824
390
c PRC016 Pre-Eclampsia 64 0.824
391
P CRV039 Cervicitis 52 0.823
393
NRL016 Neural Tube Defects 81 0.810
394
P ACT028 Acute Closed-Angle Glaucoma 32 0.810
395
P MYP006 Myopia 55 0.810
396
P CRN035 Cranial Nerve Palsy 42 0.810
397
HYP066 Hyperglycemia 60 0.810
398
P ACT105 Acute Mountain Sickness 52 0.810
400
PMP014 Pemphigoid 49 0.803
401
STT041 Stuttering 52 0.803
402
MLG169 Malignant Astrocytoma 57 0.803
403
BLL006 Bullous Pemphigoid 61 0.803
404
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.796
405
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.796
406
BRN004 Brain Edema 54 0.796
407
CDQ001 Cauda Equina Syndrome 37 0.796
408
P CHL002 Childhood Absence Epilepsy 63 0.781
409
LPD008 Lipid Metabolism Disorder 61 0.781
410
ADJ001 Adjustment Disorder 46 0.781
411
CSL001 Causalgia 44 0.781
412
c TYP008 Type 1 Diabetes Mellitus 77 0.765
413
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.765
414
P ATR011 Atrial Fibrillation 66 0.765
415
SYR010 Syringomyelia, Noncommunicating Isolated 36 0.765
416
P END044 Endometriosis 62 0.765
417
AGR002 Agoraphobia 45 0.765
418
P ECL001 Eclampsia 52 0.765
419
P SYR001 Syringomyelia 47 0.765
420
c CNT068 Central Pain Syndrome 28 0.765
421
WLS001 Wilson Disease 70 0.763
422
HYP264 Hypertonia 36 0.763
423
GRM010 Germ Cells Tumors 33 0.763
424
c GLL024 Gallbladder Disease 1 53 0.762
425
CGN007 Cognitive Function 1, Social 26 0.762
426
MCN017 Meconium Ileus 52 0.762
427
SPR126 Superior Semicircular Canal Dehiscence 41 0.762
428
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.762
429
APN008 Apnea, Obstructive Sleep 66 0.762
430
PPL049 Papillon-Lefevre Syndrome 65 0.762
431
SCK003 Sickle Cell Anemia 74 0.762
432
CHL013 Cholecystolithiasis 37 0.762
433
LYM040 Lymphoblastic Lymphoma 53 0.762
434
ANL022 Anal Fistula 47 0.762
435
ANS012 Anus Disease 47 0.762
436
SPS003 Spastic Diplegia 52 0.762
437
DVR001 Diverticulitis of Colon 24 0.762
438
HGH043 High Grade Glioma 46 0.762
439
CLN045 Colonic Benign Neoplasm 48 0.762
440
STM007 Stomatitis 52 0.762
441
MXD026 Mixed Glioma 45 0.762
442
CHL079 Children's Interstitial Lung Disease 26 0.762
443
DVR002 Diverticulitis 46 0.762
444
c HMG029 Hemoglobin Se Disease 41 0.762
445
LYM019 Lymphosarcoma 46 0.762
446
CRV043 Cervical Dystonia 45 0.748
447
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.748
448
SPR004 Supravalvular Aortic Stenosis 57 0.748
449
ENT004 Enthesopathy 51 0.748
450
PHN011 Phenytoin Toxicity 32 0.730
451
BNR002 Bone Resorption Disease 47 0.730
452
ENT011 Enterocolitis 55 0.730
453
FCL022 Focal Dystonia 41 0.730
454
PRS021 Prostatic Adenoma 43 0.730
455
BLR008 Bilirubin Metabolic Disorder 57 0.730
456
P RHN004 Rhinitis 57 0.730
457
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.730
458
RST023 Resting Heart Rate, Variation in 40 0.730
459
CYC005 Cyclothymic Disorder 40 0.730
460
TRG017 Trigeminal Trophic Syndrome 16 0.730
461
PRN019 Perinatal Necrotizing Enterocolitis 60 0.730
462
P RTN008 Retinitis Pigmentosa 79 0.711
463
VRC005 Varicose Veins 59 0.711
464
AST006 Astigmatism 46 0.711
465
c MCR115 Microvascular Complications of Diabetes 5 65 0.711
466
P INF037 Inflammatory Bowel Disease 53 0.711
467
NRR001 Neuroretinitis 42 0.711
468
PRT013 Portal Hypertension 59 0.711
469
TNG007 Tongue Carcinoma 55 0.711
470
P UVT001 Uveitis 57 0.711
471
ISC004 Ischemia 61 0.711
472
PRS045 Prostatic Hypertrophy 52 0.711
473
ESP002 Esophageal Varix 51 0.711
474
AMN001 Amenorrhea 53 0.711
475
P HYP086 Hypothyroidism 69 0.711
476
P ESP024 Esophagitis 60 0.711
477
VRC001 Varicocele 48 0.711
478
NRG002 Neurogenic Bladder 55 0.711
479
EXP001 Expressive Language Disorder 24 0.711
480
INT002 Intermittent Claudication 61 0.711
481
RTN023 Retinitis 45 0.711
482
P DYS021 Dysautonomia 38 0.711
483
P HYP263 Hypersomnia 40 0.711
484
P CRB059 Cerebellar Degeneration 36 0.711
485
BRC010 Brachial Plexus Lesion 34 0.711
486
ALL006 Allergic Asthma 56 0.711
487
P TRT019 Torticollis 47 0.690
488
FRN006 Frontotemporal Dementia 68 0.690
489
c EPS037 Episodic Ataxia, Type 4 28 0.690
490
P OPN001 Open-Angle Glaucoma 55 0.690
491
MYL020 Myelomeningocele 51 0.690
492
EXF001 Exfoliation Syndrome 56 0.690
493
P OPT006 Optic Nerve Disease 57 0.690
494
HDR003 Hidradenitis 50 0.690
495
c HRD010 Hereditary Spastic Paraplegia 65 0.690
496
VGN017 Vaginal Cancer 58 0.690
497
MTS001 Mutism 44 0.690
498
PPT005 Peptic Ulcer Disease 58 0.690
499
APP008 Appendicitis 62 0.690
500
PRL008 Paralytic Ileus 44 0.690
501
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 21 0.690
502
HMC014 Homocysteinemia 52 0.666
503
P MDL005 Medulloblastoma 75 0.666
504
PLN026 Pilonidal Sinus 35 0.666
505
c ATR087 Atrial Standstill 1 74 0.666
506
c SML038 Small Cell Cancer of the Lung 69 0.666
507
BRD004 Borderline Personality Disorder 53 0.666
508
AVD001 Avoidant Personality Disorder 49 0.666
509
P MGR003 Migraine with Aura 51 0.666
510
LMY002 Leiomyoma 51 0.666
511
P BLP003 Blepharospasm 45 0.666
512
CNV002 Conversion Disorder 47 0.666
513
P NRB001 Neuroblastoma 66 0.666
514
MYT011 Myotonia 38 0.666
515
c ACT134 Acute Liver Failure 57 0.666
516
MYC006 Mycosis Fungoides 65 0.640
517
ADR040 Adrenal Gland Pheochromocytoma 45 0.640
518
DRG024 Drug Allergy 40 0.640
519
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 0.640
520
P PHC003 Pheochromocytoma 70 0.640
521
c SYS001 Systemic Lupus Erythematosus 86 0.640
522
CRD223 Cardiac Arrhythmia 63 0.640
523
ADN018 Adenoma 58 0.640
524
P NTR004 Neutropenia 62 0.640
525
LYM017 Lyme Disease 63 0.640
526
VLV036 Vulvar Disease 47 0.640
527
KRN002 Kearns-Sayre Syndrome 63 0.640
528
P LPS004 Lupus Erythematosus 61 0.640
529
P DBT009 Diabetes Mellitus 67 0.640
530
SVR001 Severe Acute Respiratory Syndrome 68 0.620
531
P MCH002 Machado-Joseph Disease 63 0.609
532
LSC001 Lesch-Nyhan Syndrome 62 0.609
533
c PSR021 Psoriasis 14, Pustular 57 0.609
534
ASP007 Aspiration Pneumonia 49 0.609
535
KLN009 Kleine-Levin Hibernation Syndrome 37 0.609
536
c SPS147 Spastic Paraplegia 4, Autosomal Dominant 55 0.609
537
ERY061 Erythroderma, Congenital, with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-Ige 38 0.609
538
CHL122 Cholesteatoma of Middle Ear 51 0.609
539
P ART005 Arteriovenous Malformation 65 0.609
540
SVR004 Severe Combined Immunodeficiency 71 0.609
541
PLC006 Placental Choriocarcinoma 38 0.609
542
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.609
543
WRN003 Wernicke Encephalopathy 45 0.609
544
c CHR087 Chronic Cystitis 37 0.609
545
CRN009 Corneal Ectasia 29 0.609
546
FST001 Foster-Kennedy Syndrome 39 0.609
547
ALC006 Alcoholic Hepatitis 61 0.609
548
CHR074 Choriocarcinoma 46 0.609
549
P EPD016 Epidermolysis Bullosa 53 0.609
550
PLM029 Palmoplantar Keratosis 48 0.609
551
CNT067 Central Cord Syndrome 20 0.609
552
THN005 Thunderclap Headache 15 0.609
553
FMR003 Femoral Neuropathy 35 0.609
554
LMY003 Leiomyomatosis 43 0.609
555
INT020 Intravenous Leiomyomatosis 36 0.609
556
P HYP087 Hypotrichosis 41 0.609
557
MXL017 Maxillary Cancer 31 0.609
558
P HYP076 Hyperthyroidism 53 0.609
559
P FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 39 0.609
560
c SPS091 Spastic Paraplegia 4 27 0.609
561
RCR002 Recurrent Hypersomnia 27 0.609
562
EPL230 Epilepsy with Myoclonic-Atonic Seizures 23 0.609
563
LYM053 Lymphomatous Thyroiditis 22 0.609
564
OCL024 Ocular Neuromyotonia 12 0.609
565
P PST059 Pustular Psoriasis 37 0.609
566
DSR074 Disorder of Purine Metabolism 23 0.609
567
P OVR082 Overgrowth Syndrome 42 0.609
568
P HYP265 Hypotonia 42 0.599
569
RCK004 Rickets 65 0.576
570
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.568
571
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.568
572
IMM167 Immune Deficiency Disease 77 0.568
573
P CTN015 Cutaneous T Cell Lymphoma 48 0.568
574
OCL066 Oculogyric Crisis 34 0.568
575
ACT003 Acute Kidney Tubular Necrosis 46 0.568
576
GYN001 Gynecomastia 48 0.568
577
INF021 Infant Gynecomastia 30 0.568
578
TST014 Testicular Cancer 51 0.568
579
GNG012 Gingival Overgrowth 49 0.568
580
ART002 Arts Syndrome 66 0.568
581
c RTN047 Retinitis Pigmentosa 18 45 0.568
582
P THY032 Thyroiditis 56 0.568
583
PLY024 Polymicrogyria 46 0.568
584
CHR178 Chromosomal Triplication 34 0.568
585
PRT036 Peritonitis 65 0.568
586
SCN086 Scn9a Neuropathic Pain Syndromes 8 0.568
587
CGT001 Ciguatera Fish Poisoning 20 0.568
588
EXN003 Exencephaly 30 0.568
589
LWG005 Low-Grade Astrocytoma 38 0.568
591
SPN019 Spondylolisthesis 52 0.550
592
c ACT068 Acute Cystitis 61 0.550
593
WST001 West Syndrome 64 0.539
594
MYL069 Myeloma, Multiple 77 0.518
595
HMN044 Human Immunodeficiency Virus Type 1 76 0.518
596
CLT003 Colitis 63 0.518
598
P APL001 Aplastic Anemia 73 0.511
599
PHB001 Phobic Disorder 45 0.505
600
CVD001 Covid-19 58 0.478
601
HYP025 Hyperphosphatemia 47 0.478
602
BLD051 Blood Coagulation Disease 53 0.478
603
GLC096 Galactorrhea 40 0.470
604
HYP020 Hyperprolactinemia 63 0.470
605
LMB062 Limb Ischemia 55 0.470
606
NTR042 Neutrophilic Dermatosis, Acute Febrile 56 0.470
607
P NNN008 Noonan Syndrome 1 76 0.470
608
P ESN008 Eosinophilic Pneumonia 50 0.470
609
CHL067 Cholecystitis 59 0.470
610
TLS001 Tolosa-Hunt Syndrome 34 0.470
611
VLV008 Vulvitis 31 0.470
612
MCL006 Macular Retinal Edema 56 0.470
613
GRN003 Granulomatous Dermatitis 32 0.470
614
PRM003 Premature Ejaculation 44 0.470
615
RYN005 Raynaud Phenomenon 45 0.470
616
P PNM007 Pneumonia 64 0.470
617
c PSD047 Pseudo-Turner Syndrome 52 0.470
618
FXD003 Fixed Drug Eruption 34 0.470
619
CTN031 Cutaneous Pseudolymphoma 16 0.470
620
c ERL020 Early-Onset Schizophrenia 43 0.470
621
NRM005 Neuromuscular Disease 63 0.417
622
ATN005 Autonomic Dysfunction 45 0.381
623
c FNC043 Fanconi Anemia, Complementation Group E 62 0.379
624
PRP001 Propionic Acidemia 65 0.379
625
KWS002 Kawasaki Disease 65 0.379
626
CMR002 Coumarin Resistance 60 0.379
627
CHN016 Cohen Syndrome 59 0.379
628
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.379
629
GST071 Gastrointestinal Carcinoma 46 0.379
630
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.379
631
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.379
632
ACQ007 Acquired Immunodeficiency Syndrome 58 0.379
633
PLS009 Plasma Cell Neoplasm 64 0.379
634
FCL011 Facial Nerve Disease 38 0.379
635
RCT017 Rectal Disease 49 0.379
636
GNC005 Geniculate Ganglionitis 29 0.379
637
CNN003 Conn's Syndrome 77 0.379
638
CNT033 Central Nervous System Cancer 47 0.379
639
P ART023 Arthropathy 60 0.379
640
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.379
641
GST049 Gastrointestinal System Cancer 49 0.379
642
OST022 Osteopathia Striata with Cranial Sclerosis 54 0.379
643
HYP005 Hypokalemia 55 0.379
644
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.379
645
ULC004 Ulcerative Colitis 74 0.379
646
CYS021 Cystic Adenomatoid Malformation of Lung 32 0.379
647
GGN004 Gigantomastia 25 0.379
648
MNC020 Monoclonal Mast Cell Activation Syndrome 20 0.379
649
TMP019 Temporomandibular Joint Anomaly 28 0.368
650
P EPL140 Epilepsy, Idiopathic Generalized 60 0.355
651
P PTS002 Ptosis 52 0.355
652
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 0.355
653
URM002 Uremia 47 0.326
654
PRP027 Peripheral Vascular Disease 71 0.311
655
P EPL198 Epilepsy, Myoclonic Juvenile 61 0.295
656
BRN024 Bronchitis 67 0.295
657
P BNC003 Bone Cancer 58 0.278
658
VST001 Vestibular Neuronitis 33 0.278
659
PLM010 Pulmonary Edema 54 0.278
660
ATN004 Autonomic Neuropathy 42 0.278
661
DMY004 Demyelinating Disease 50 0.278
662
MYL001 Myelitis 49 0.278
663
DRV001 Dravet Syndrome 70 0.278
664
HPT004 Hepatic Coma 43 0.260
665
NPH009 Nephrolithiasis 54 0.260
666
P MLN008 Melanoma 75 0.260
667
HPT019 Hepatic Encephalopathy 59 0.260
668
ABD002 Abducens Nerve Disease 38 0.260
669
SHR117 Short-Lasting Unilateral Neuralgiform Headache Attacks with Cranial Autonomic Symptoms 11 0.260
670
HDN002 Head Injury 44 0.260
671
c EPS035 Episodic Ataxia, Type 2 63 0.241
672
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.241
673
TBC004 Tobacco Addiction 63 0.241
674
CHL061 Childhood Leukemia 47 0.241
675
P AXN001 Axonal Neuropathy 33 0.241
676
NRM001 Neuromyelitis Optica 60 0.241
677
END057 Endometrial Cancer 71 0.220
678
c HYP836 Hypercholesterolemia, Familial, 1 73 0.220
679
P BND020 Bone Disease 60 0.220
680
P TRN034 Transverse Myelitis 47 0.220
681
ACT078 Acute Porphyria 50 0.220
682
P GND004 Gonadal Dysgenesis 46 0.220
683
PLX004 Plexopathy 29 0.220
684
c GM2006 Gm2 Gangliosidosis 46 0.220
685
P GNG009 Gangliosidosis 44 0.220
686
PRX009 Paroxysmal Hemicrania 32 0.220
687
PRT058 Pure Autonomic Failure 58 0.220
688
PRS120 Persistent Idiopathic Facial Pain 27 0.220
689
ANG054 Angina Pectoris 65 0.197
690
OST011 Osteomalacia 52 0.197
691
FML037 Female Breast Cancer 51 0.197
692
P JVN007 Juvenile Absence Epilepsy 47 0.197
693
c EPL133 Epilepsy, Juvenile Absence 1 46 0.197
694
P MYC007 Myocardial Infarction 69 0.197
695
MNR012 Meniere Disease 55 0.197
696
MTN003 Motion Sickness 50 0.197
697
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.197
698
STF001 Stiff-Person Syndrome 57 0.197
699
KRT019 Keratitis, Hereditary 66 0.197
700
GT001 Gout 63 0.197
701
P DRR001 Diarrhea 55 0.197
702
P HYP040 Hypospadias 51 0.197
703
P MCR010 Microcephaly 59 0.197
704
HYP080 Hypogonadism 49 0.197
705
CLL003 Cellulitis 53 0.197
706
P URT039 Urticaria 57 0.197
707
BNG009 Benign Epilepsy with Centrotemporal Spikes 60 0.197
708
P ORT004 Orthostatic Intolerance 62 0.197
709
FTD001 Foot Drop 36 0.197
710
CHR066 Chronic Fatigue Syndrome 60 0.197
711
P MTC069 Mitochondrial Disorders 57 0.197
712
P ENC004 Encephalitis 61 0.197
713
PRS053 Parsonage Turner Syndrome 22 0.197
714
P CHN012 Chondrosarcoma 56 0.170
715
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.170
716
HLX001 Helix Syndrome 47 0.170
717
P SNS001 Sensorineural Hearing Loss 59 0.170
718
AMB002 Amblyopia 49 0.170
719
PLV003 Pelvic Inflammatory Disease 54 0.170
720
P DRM010 Dermatomyositis 61 0.170
721
SPP007 Suppression Amblyopia 38 0.170
722
PRM013 Premature Menopause 57 0.170
723
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.170
724
P RHM011 Rheumatoid Arthritis 81 0.170
725
APH002 Aphasia 55 0.170
726
P CRD119 Cardiac Arrest 68 0.170
727
APR001 Apraxia 51 0.170
728
c RST020 Restless Legs Syndrome 6 21 0.170
729
MLT157 Multiple System Atrophy 1 69 0.170
730
SPN354 Spinal Arachnoiditis 35 0.170
731
MNN009 Meningoencephalitis 48 0.170
732
PTH002 Pathological Gambling 48 0.170
733
CNT047 Contact Dermatitis 57 0.170
734
P DMY001 Demyelinating Polyneuropathy 41 0.170
735
TXC005 Toxic Shock Syndrome 62 0.170
736
P EHL001 Ehlers-Danlos Syndrome 57 0.170
737
P OPT009 Optic Neuritis 57 0.170
738
CGH001 Cough Variant Asthma 34 0.170
739
ARC002 Arachnoiditis 49 0.170
740
GST037 Gastroparesis 52 0.170
741
HDR002 Hidradenitis Suppurativa 54 0.170
742
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.170
743
P GST044 Gastritis 55 0.170
744
HYP707 Hypertrophic Olivary Degeneration 18 0.170
745
OCC008 Occipital Neuralgia 24 0.170
746
DGN001 Degenerative Disc Disease 48 0.170
747
INT075 Intracranial Hypertension 52 0.170
748
CLF001 Cleft Lip 54 0.170
749
CRB001 Cerebral Lymphoma 36 0.170
750
P FBR031 Febrile Seizures 52 0.170
751
RMS001 Rem Sleep Behavior Disorder 47 0.170
752
HRN003 Heroin Dependence 44 0.170
753
TYL001 Taylor's Syndrome 30 0.170
754
HRP011 Herpes Zoster Ophthalmicus 24 0.170
755
NWD001 New Daily-Persistent Headache 19 0.170
756
PSD088 Pseudobulbar Affect 33 0.170
757
PYR016 Pyridoxine Deficiency 29 0.170
758
MTC196 Mitochondrial Disease with Epilepsy 9 0.170
759
RRH030 Rare Headache 12 0.170
761
OCL015 Oculomotor Apraxia 39 0.170
762
TRT020 Tritanopia 49 0.139
763
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.139
764
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.139
765
PRT251 Proteinuria, Chronic Benign 58 0.139
766
DYS001 Dyskinetic Cerebral Palsy 31 0.139
767
GLC003 Glucose Intolerance 53 0.139
768
P LKD001 Leukodystrophy 58 0.139
769
P VNS003 Venous Insufficiency 54 0.139
770
BNS007 Bone Sarcoma 51 0.139
771
SPN221 Spina Bifida Occulta 39 0.139
772
END062 Endometrial Hyperplasia 48 0.139
773
P OST002 Osteoporosis 77 0.139
774
ESN015 Eosinophilic Fasciitis 46 0.139
775
P LPR021 Leprosy 3 71 0.139
776
c DWL002 Dowling-Degos Disease 1 58 0.139
777
c TRM024 Tremor, Hereditary Essential, 1 34 0.139
778
SPS007 Spastic Cerebral Palsy 46 0.139
779
GRN004 Granulomatous Amebic Encephalitis 30 0.139
780
P MYC084 Mycobacterium Tuberculosis 1 68 0.139
781
PHB003 Phobia, Specific 44 0.139
782
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.139
783
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 0.139
784
IMM162 Immunoglobulin E Concentration, Serum 28 0.139
785
CNT106 Centralopathic Epilepsy 34 0.139
786
ANS021 Anisocoria 25 0.139
787
ATM095 Autoimmune Disease 61 0.139
788
MYC078 Myoclonus and Ataxia 31 0.139
789
CRD132 Cardiac Conduction Defect 59 0.139
790
CLF027 Cleft Palate, Isolated 64 0.139
791
TRC010 Trichotillomania 50 0.139
792
IMP006 Impulse Control Disorder 45 0.139
793
ANT011 Antisocial Personality Disorder 47 0.139
794
HMP005 Hemiplegia 53 0.139
795
c VRL010 Viral Hepatitis 52 0.139
796
OST017 Osteomyelitis 63 0.139
797
PHY002 Physical Disorder 41 0.139
798
CRN019 Coronary Artery Vasospasm 47 0.139
799
P TBR001 Tuberous Sclerosis 69 0.139
800
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 0.139
801
PNM008 Pneumothorax 54 0.139
802
HYP014 Hyperuricemia 51 0.139
803
P HYP069 Hyperparathyroidism 62 0.139
804
FRZ001 Frozen Shoulder 54 0.139
805
FCL012 Facial Paralysis 49 0.139
806
VST003 Vestibular Nystagmus 25 0.139
807
PPL021 Papilledema 49 0.139
808
ATY001 Atypical Depressive Disorder 45 0.139
809
HYP043 Hyperandrogenism 47 0.139
810
P HRN001 Horner's Syndrome 45 0.139
811
P ADL010 Adult Respiratory Distress Syndrome 71 0.139
812
INT066 Interstitial Lung Disease 60 0.139
813
MYF001 Myofibroma 42 0.139
814
NRL005 Neurilemmoma 60 0.139
815
SPN041 Spinal Cord Disease 54 0.139
816
SPS019 Spastic Paraparesis 38 0.139
817
P SYS005 Systemic Scleroderma 73 0.139
818
P INT099 Intrahepatic Cholestasis of Pregnancy 61 0.139
819
P MRC003 Mercury Poisoning 48 0.139
820
VLV042 Vulvar Vestibulitis Syndrome 37 0.139
821
P NRC002 Narcolepsy 55 0.139
822
P LCH002 Lichen Planus 55 0.139
824
FSC004 Fasciitis 49 0.139
825
LNG099 Lung Disease 62 0.139
826
INT042 Internuclear Ophthalmoplegia 32 0.139
827
NRV004 Nerve Compression Syndrome 47 0.139
828
ALL014 Allergic Encephalomyelitis 34 0.139
829
P CHR342 Chiari Malformation 41 0.139
830
ALB002 Albinism 47 0.139
831
PLM033 Pulmonary Embolism 58 0.139
832
PST021 Postpartum Depression 50 0.139
833
CRM010 Cramp-Fasciculation Syndrome 17 0.139
834
HNS001 Hansen's Disease 32 0.139
835
P TXP001 Toxoplasmosis 60 0.139
836
ACN019 Acanthamoeba Keratitis 30 0.139
837
PST092 Posttransplant Acute Limbic Encephalitis 29 0.139
838
TRG013 Trigeminal Autonomic Cephalalgia 15 0.139
839
DRG017 Drug-Induced Vasculitis 16 0.139
840
ESN022 Eosinophilic Colitis 24 0.139
841
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 26 0.139
842
c MYC068 Myoclonic Epilepsy of Infancy 34 0.139
843
P SRC025 Sarcoidosis 1 70 0.098
844
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.098
845
HYL004 Hyaline Fibromatosis Syndrome 66 0.098
846
LYM133 Lymphoma, Hodgkin, Classic 74 0.098
847
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.098
848
PRS129 Prostatic Hyperplasia, Benign 48 0.098
849
LGH007 Leigh Syndrome 70 0.098
850
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 36 0.098
851
MYC079 Myoclonic Epilepsy of Lafora 63 0.098
852
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.098
853
INS024 Insulin-Like Growth Factor I 77 0.098
855
c MYT020 Myotonic Dystrophy 2 57 0.098
856
c BRN108 Branchiootic Syndrome 1 63 0.098
857
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.098
858
INT333 Intellectual Developmental Disorder with Autism and Speech Delay 29 0.098
859
MSC007 Muscle Hypertrophy 64 0.098
860
P TMR010 Tumor Predisposition Syndrome 69 0.098
861
c PRM108 Primary Progressive Multiple Sclerosis 51 0.098
862
DSS032 Disease by Infectious Agent 55 0.098
863
LWG006 Low Grade Glioma 41 0.098
864
MLD018 Mild Cognitive Impairment 48 0.098
865
AMY003 Amyotrophic Neuralgia 41 0.098
866
P CHR071 Charcot-Marie-Tooth Disease 64 0.098
867
PRT019 Protein-Losing Enteropathy 44 0.098
868
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.098
869
P PLY041 Polymyositis 59 0.098
870
CHR710 Chronic Spontaneous Urticaria 45 0.098
871
c CHR699 Charcot-Marie-Tooth Disease Type 2a2a 28 0.098
872
CYS005 Cysticercosis 60 0.098
873
P RNL015 Renal Hypertension 45 0.098
874
MCR037 Macroglossia 44 0.098
875
OTT002 Otitis Media 71 0.098
876
PRX015 Paroxysmal Extreme Pain Disorder 56 0.098
877
P OVR042 Ovarian Cancer 88 0.098
878
ACN002 Acanthosis Nigricans 56 0.098
879
c SPN225 Spondyloarthropathy 1 70 0.098
880
ATH013 Atherosclerosis Susceptibility 63 0.098
881
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.098
882
RTN017 Retinal Detachment 60 0.098
883
KRT071 Keratosis, Seborrheic 56 0.098
884
SMT008 Smith-Magenis Syndrome 53 0.098
885
SPS134 Spasmodic Dystonia 28 0.098
886
P SPS008 Spastic Ataxia 41 0.098
887
ORL015 Oral Squamous Cell Carcinoma 43 0.098
888
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.098
889
VTM002 Vitamin B12 Deficiency 48 0.098
890
MTB004 Metabolic Acidosis 48 0.098
891
CGN006 Cogan Syndrome 49 0.098
892
HYP017 Hypophosphatemia 49 0.098
893
SGM008 Segmental Dystonia 28 0.098
894
TRC097 Tracheomalacia 43 0.098
895
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.098
896
CRB205 Cerebellar Atrophy with Seizures and Variable Developmental Delay 24 0.098
897
PRT010 Parathyroid Carcinoma 68 0.098
898
c SPN299 Spinocerebellar Ataxia 20 33 0.098
899
P DRM053 Dermatitis, Atopic 65 0.098
900
PSR001 Psoriatic Arthritis 61 0.098
901
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.098
902
c HPT073 Hepatitis C Virus 71 0.098
903
c CLR079 Colorectal Cancer 2 30 0.098
904
P LRY029 Laryngomalacia 47 0.098
905
P HYP750 Hypertriglyceridemia, Familial 62 0.098
906
DMN031 Dementia, Lewy Body 65 0.098
907
P EPS030 Episodic Kinesigenic Dyskinesia 1 55 0.098
909
P ANG001 Angelman Syndrome 65 0.098
910
OPT070 Optic Nerve Hypoplasia, Bilateral 55 0.098
911
PRP090 Peripheral Dysostosis 22 0.098
912
CRT072 Creutzfeldt-Jakob Disease 67 0.098
913
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.098
914
P LNG064 Lung Cancer Susceptibility 3 70 0.098
915
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.098
916
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.098
917
c CHR579 Chiari Malformation Type Ii 44 0.098
918
ALX003 Alexander Disease 61 0.098
919
ANN002 Anencephaly 57 0.098
920
c CHR660 Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a 36 0.098
921
EWN003 Ewing Sarcoma 70 0.098
922
SRC014 Sarcoma 64 0.098
923
P SPN052 Spondyloarthropathy 54 0.098
924
P PRP003 Porphyria Cutanea Tarda 66 0.098
925
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.098
926
SPN392 Spondylosis, Cervical 30 0.098
927
c THR092 Thrombophilia Due to Thrombin Defect 74 0.098
928
WLL001 Williams-Beuren Syndrome 60 0.098
929
P TMP003 Temporal Arteritis 68 0.098
930
DYS018 Dysostosis 43 0.098
931
PSD001 Pseudobulbar Palsy 37 0.098
932
LMB024 Limbic Encephalitis 43 0.098
933
c CHR708 Chronic Urticaria 42 0.098
934
THR024 Thrombosis 56 0.098
935
P HRD021 Hereditary Sensory Neuropathy 48 0.098
936
P PRG013 Paraganglioma 57 0.098
937
RHM028 Rheumatic Heart Disease 56 0.098
938
PTN001 Patent Foramen Ovale 62 0.098
939
CMM005 Common Cold 55 0.098
940
ANS004 Anisometropia 31 0.098
941
VLV032 Vulva Cancer 60 0.098
942
P MGR001 Migraine Without Aura 48 0.098
943
CRT013 Carotid Stenosis 51 0.098
944
DSS005 Dissociated Nystagmus 18 0.098
945
CRY004 Cryoglobulinemia 47 0.098
946
LYM027 Lymphopenia 56 0.098
947
P ACN011 Acne 55 0.098
948
P INF032 Infertility 60 0.098
949
INF013 Inferior Myocardial Infarction 33 0.098
950
SPN051 Spondylitis 51 0.098
951
CLC001 Calciphylaxis 50 0.098
952
P BNG030 Benign Ependymoma 51 0.098
953
ANG016 Angiokeratoma 37 0.098
954
P OVR046 Ovarian Cyst 44 0.098
955
GNG006 Gingival Hypertrophy 36 0.098
956
P RTN018 Retinal Disease 53 0.098
957
P ART018 Aortic Valve Insufficiency 52 0.098
958
URM001 Uremic Neuropathy 20 0.098
959
ANH002 Anhidrosis 45 0.098
960
MNN002 <