Search results for Lidocaine

1210 hits were found for Lidocaine

# Family MCID Name MIFTS Score
1
LDC001 Lidocaine Allergy 19 4.234
2
PNG002 Pain Agnosia 51 0.572
3
c PNS012 Paine Syndrome 61 0.498
4
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.494
5
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.284
6
P CHR345 Chronic Pain 50 0.276
7
P SZR006 Seizure Disorder 58 0.214
8
ALL026 Allergic Hypersensitivity Disease 64 0.207
9
48X005 48,xyyy 39 0.204
10
VSL002 Visual Epilepsy 58 0.203
11
PST053 Postherpetic Neuralgia 42 0.202
12
P CTR002 Cataract 60 0.201
13
ILS001 Ileus 51 0.195
14
P CRD119 Cardiac Arrest 67 0.189
15
ANX010 Anxiety 72 0.183
16
c ACT075 Acute Myocardial Infarction 56 0.180
17
c FNC043 Fanconi Anemia, Complementation Group E 62 0.179
18
PLP001 Pulpitis 48 0.178
19
ATX019 Ataxia with Vitamin E Deficiency 48 0.178
20
P HDC001 Headache 57 0.170
21
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.158
22
BCK006 Back Pain 42 0.158
23
P NRP001 Neuropathy 56 0.153
24
P MYC007 Myocardial Infarction 70 0.151
25
c RHB024 Rhabdomyosarcoma 2 65 0.150
26
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.149
27
MCN017 Meconium Ileus 52 0.149
28
P INT143 Interstitial Cystitis 61 0.147
29
c MGR028 Migraine with or Without Aura 1 69 0.143
30
P MTH007 Methemoglobinemia 46 0.135
31
OST012 Osteoarthritis 78 0.134
32
DPR016 Depression 63 0.134
33
P TRN020 Turner Syndrome 65 0.132
34
MNT002 Mental Depression 57 0.132
35
HRP004 Herpes Zoster 60 0.131
36
CNG034 Congestive Heart Failure 70 0.129
37
PHR003 Pharyngitis 56 0.128
38
MYF002 Myofascial Pain Syndrome 42 0.128
39
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.124
40
P CYS018 Cystitis 59 0.124
41
FBR047 Fibromyalgia 59 0.124
42
DBT010 Diabetic Neuropathy 55 0.124
43
TRG002 Trigeminal Neuralgia 60 0.123
44
STT001 Status Epilepticus 59 0.121
45
CMP010 Complex Regional Pain Syndrome 58 0.121
46
c HYP595 Hypertension, Essential 84 0.119
47
P CNR004 Cone-Rod Dystrophy 2 71 0.119
48
ISC004 Ischemia 60 0.119
49
SPN186 Spinal Cord Injury 60 0.119
50
CYT002 Cytokine Deficiency 44 0.119
51
CRP001 Carpal Tunnel Syndrome 67 0.117
52
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.117
53
CHL079 Children's Interstitial Lung Disease 27 0.117
54
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.115
55
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.114
56
P LVR013 Liver Disease 68 0.112
57
P CLR023 Colorectal Cancer 98 0.110
58
ADL002 Adult Syndrome 69 0.110
59
CNS004 Constipation 57 0.110
60
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.110
61
P PRP019 Peripheral Nervous System Disease 57 0.108
62
P HRT032 Heart Disease 75 0.104
63
P PLY019 Polyneuropathy 56 0.104
64
P BRS047 Breast Cancer 96 0.100
65
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.100
66
P KDN018 Kidney Disease 70 0.098
67
ATR057 Atrioventricular Block 55 0.096
68
RDC002 Radiculopathy 48 0.096
69
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.094
70
DRM006 Dermatitis 61 0.094
71
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.094
72
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.094
73
OCL069 Ocular Motor Apraxia 51 0.094
74
NRM004 Neuroma 51 0.094
75
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.094
76
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.094
77
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.094
78
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.094
79
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.094
80
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.094
81
PRM003 Premature Ejaculation 44 0.094
82
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.094
83
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.094
84
P ART022 Arthritis 70 0.091
85
CRB039 Cerebrovascular Disease 69 0.091
86
ING001 Inguinal Hernia 60 0.091
87
P TRM003 Tremor 53 0.091
88
PRS063 Paresthesia 43 0.091
89
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.091
90
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.091
91
STR067 Stroke, Ischemic 80 0.089
92
DYS073 Dysphagia 50 0.089
93
KRT013 Keratolytic Winter Erythema 46 0.089
94
THR024 Thrombosis 56 0.087
95
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.087
96
P LNG028 Long Qt Syndrome 65 0.084
97
P EXN002 Exanthem 57 0.084
98
P STR020 Strabismus 56 0.084
99
RFL001 Reflex Sympathetic Dystrophy 53 0.084
100
P HMR005 Hemorrhoid 46 0.084
101
MCH006 Mechanical Strabismus 39 0.084
102
c THR092 Thrombophilia Due to Thrombin Defect 73 0.082
103
P ATR011 Atrial Fibrillation 66 0.082
104
LVR012 Liver Cirrhosis 63 0.082
105
CRD223 Cardiac Arrhythmia 60 0.082
106
CNT047 Contact Dermatitis 57 0.082
107
FRZ001 Frozen Shoulder 53 0.082
108
c LRG017 Large Intestine Cancer 47 0.082
109
DWN001 Down Syndrome 70 0.079
110
P NRV007 Nervous System Disease 66 0.079
111
HYP266 Hypoxia 56 0.079
112
HYP005 Hypokalemia 55 0.079
113
SBC016 Subacute Delirium 44 0.079
114
RDN001 Reading Disorder 40 0.079
115
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.079
116
P LNG032 Lung Cancer 97 0.076
117
P RSP003 Respiratory Failure 74 0.076
118
P MNN013 Meningitis 65 0.076
119
P VSC007 Vascular Disease 63 0.076
120
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.076
121
DBT004 Diabetic Polyneuropathy 50 0.076
122
BRS064 Bursitis 47 0.076
123
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.074
124
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.074
125
P CRN018 Coronary Artery Anomaly 63 0.074
126
MCS002 Mucositis 55 0.074
127
PTH003 Pathologic Nystagmus 51 0.074
128
BRN071 Brain Injury 49 0.074
129
47X002 47,xyy 49 0.074
130
VLV042 Vulvar Vestibulitis Syndrome 40 0.074
131
ENT001 Enterocele 39 0.074
132
ALG001 Algoneurodystrophy 39 0.074
133
RRS014 Rare Surgical Neurologic Disease 32 0.074
134
P SKN015 Skin Carcinoma 67 0.071
135
c MCR129 Microvascular Complications of Diabetes 1 66 0.071
136
c ACT068 Acute Cystitis 63 0.071
137
P PLV020 Pelvic Organ Prolapse 59 0.071
138
PLM010 Pulmonary Edema 55 0.071
139
INT075 Intracranial Hypertension 53 0.071
140
TND005 Tendinitis 52 0.071
141
c GLL024 Gallbladder Disease 1 52 0.071
142
TND004 Tendinopathy 44 0.071
143
P CLS010 Cluster Headache 43 0.071
144
LWC001 Low Compliance Bladder 42 0.071
145
P BLD134 Bladder Cancer 78 0.068
146
P EPL164 Epilepsy 71 0.068
147
P PNM007 Pneumonia 68 0.068
148
P GLL020 Gallbladder Disease 58 0.068
149
P INF032 Infertility 57 0.068
150
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.068
151
P CRD246 Cardiovascular System Disease 56 0.068
152
BHR001 Behr Syndrome 49 0.068
153
CYN002 Cyanosis, Transient Neonatal 45 0.068
154
EPC002 Epicondylitis 41 0.068
155
KLD004 Keloid Disorder 40 0.068
156
SHL001 Shoulder Impingement Syndrome 33 0.068
157
P PRS040 Prostate Cancer 97 0.065
158
P NRF023 Neurofibromatosis, Type Ii 76 0.065
159
DFC004 Deficiency Anemia 75 0.065
160
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.065
161
TXC005 Toxic Shock Syndrome 61 0.065
162
LNG099 Lung Disease 61 0.065
163
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.065
164
PNM008 Pneumothorax 56 0.065
165
TRM010 Traumatic Brain Injury 53 0.065
166
PRL008 Paralytic Ileus 44 0.065
167
SPS057 Spasticity 41 0.065
168
RRD056 Rare Disease in Surgical Orthopedic 28 0.065
169
AST005 Asthma 77 0.061
170
LPT014 Leptin Deficiency or Dysfunction 73 0.061
171
P OST002 Osteoporosis 73 0.061
172
P HYP086 Hypothyroidism 68 0.061
173
ANG054 Angina Pectoris 66 0.061
174
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.061
175
c MCL013 Mucolipidosis Iv 64 0.061
176
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.061
177
P CRN300 Coronary Heart Disease 1 63 0.061
178
SKN016 Skin Disease 63 0.061
179
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.061
180
P PRD008 Periodontitis 62 0.061
181
P ENC018 Encephalopathy 61 0.061
182
P SNS001 Sensorineural Hearing Loss 61 0.061
183
ANR040 Aneurysm 58 0.061
184
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.061
185
ANG005 Anogenital Venereal Wart 56 0.061
186
CMM005 Common Cold 56 0.061
187
ALL010 Allergic Contact Dermatitis 55 0.061
188
AMN003 Amnestic Disorder 54 0.061
189
ART140 Arteries, Anomalies of 53 0.061
190
P ECL001 Eclampsia 51 0.061
191
CHL004 Cholelithiasis 49 0.061
192
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.061
193
SMT001 Somatization Disorder 48 0.061
194
P MYC033 Myoclonus 46 0.061
195
SYN036 Syncope 45 0.061
196
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.061
197
CDQ001 Cauda Equina Syndrome 39 0.061
198
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.061
199
c PRS136 Prostate Cancer, Hereditary, 6 33 0.061
200
c PRS130 Prostate Cancer, Hereditary, 8 32 0.061
202
P GST053 Gastric Cancer 83 0.058
203
SCK003 Sickle Cell Anemia 72 0.058
204
P PHC003 Pheochromocytoma 71 0.058
205
P SYS005 Systemic Scleroderma 70 0.058
206
MLN008 Melanoma 69 0.058
207
P SLP006 Sleep Apnea 69 0.058
208
PRT036 Peritonitis 65 0.058
209
P ADL010 Adult Respiratory Distress Syndrome 63 0.058
210
c SCL052 Scleroderma, Familial Progressive 62 0.058
211
NTR005 Nutritional Deficiency Disease 61 0.058
212
ACQ007 Acquired Immunodeficiency Syndrome 60 0.058
213
PNM010 Pneumothorax, Primary Spontaneous 60 0.058
214
P SCL018 Scoliosis 60 0.058
215
P URT039 Urticaria 58 0.058
216
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.058
217
MTH009 Mouth Disease 56 0.058
218
P MYP006 Myopia 55 0.058
219
KRT009 Keratosis 53 0.058
220
P PTS002 Ptosis 52 0.058
221
P END047 Endophthalmitis 52 0.058
222
LMY002 Leiomyoma 50 0.058
223
OPT003 Opiate Dependence 50 0.058
224
MTB004 Metabolic Acidosis 50 0.058
225
MLL001 Molluscum Contagiosum 49 0.058
226
P ERY008 Erythromelalgia 47 0.058
227
ADR040 Adrenal Gland Pheochromocytoma 46 0.058
228
ORB013 Orbital Disease 42 0.058
229
P HYP265 Hypotonia 42 0.058
230
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.058
231
CRV035 Cervical Cancer 76 0.054
232
P MLT020 Multiple Sclerosis 72 0.054
233
P OCL013 Oculodentodigital Dysplasia 69 0.054
234
c BSL007 Basal Cell Carcinoma 68 0.054
235
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.054
236
WLF001 Wolff-Parkinson-White Syndrome 65 0.054
237
IRR002 Irritable Bowel Syndrome 63 0.054
238
MSC007 Muscle Hypertrophy 63 0.054
239
c PRC016 Pre-Eclampsia 63 0.054
240
P ART023 Arthropathy 62 0.054
241
VRC005 Varicose Veins 60 0.054
242
THY029 Thyroid Carcinoma 59 0.054
243
c ACT071 Acute Kidney Failure 59 0.054
244
THY122 Thyroid Gland Cancer 58 0.054
245
END030 End Stage Renal Failure 58 0.054
246
c DWL002 Dowling-Degos Disease 1 58 0.054
247
AGN016 Aging 56 0.054
248
c INT072 Intestinal Pseudo-Obstruction 56 0.054
249
PRS045 Prostatic Hypertrophy 52 0.054
250
P ACT008 Actinic Keratosis 52 0.054
251
PRS021 Prostatic Adenoma 51 0.054
252
THY030 Thyroid Gland Disease 51 0.054
253
STM007 Stomatitis 49 0.054
254
PRS129 Prostatic Hyperplasia, Benign 49 0.054
255
LPT006 Leptin Receptor Deficiency 47 0.054
256
RYN005 Raynaud Phenomenon 46 0.054
257
OPD001 Opioid Abuse 45 0.054
258
CSL001 Causalgia 45 0.054
259
VGN019 Vaginal Discharge 44 0.054
260
DBT002 Diabetic Autonomic Neuropathy 41 0.054
261
FML039 Female Reproductive System Disease 38 0.054
262
CHL013 Cholecystolithiasis 37 0.054
263
OCC008 Occipital Neuralgia 25 0.054
264
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.050
265
PRP027 Peripheral Vascular Disease 71 0.050
266
P NRB001 Neuroblastoma 71 0.050
267
RCK004 Rickets 69 0.050
268
BRN024 Bronchitis 68 0.050
269
P MLG056 Malignant Hyperthermia 67 0.050
270
c JVN010 Juvenile Rheumatoid Arthritis 67 0.050
271
ALC007 Alcohol Dependence 66 0.050
272
TTN003 Tetanus 64 0.050
273
c MLN065 Melanocytic Nevus Syndrome, Congenital 63 0.050
274
P END044 Endometriosis 62 0.050
275
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.050
276
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.050
277
RTN017 Retinal Detachment 60 0.050
278
SQM006 Squamous Cell Carcinoma 60 0.050
279
SPN027 Spinal Stenosis 59 0.050
280
MNR012 Meniere Disease 57 0.050
281
P END033 Endocarditis 57 0.050
282
TNS005 Tonsillitis 57 0.050
283
P INF037 Inflammatory Bowel Disease 56 0.050
284
INT030 Intracranial Aneurysm 56 0.050
285
P HYP076 Hyperthyroidism 55 0.050
286
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.050
287
P SBS003 Substance Abuse 54 0.050
288
END040 Endogenous Depression 54 0.050
289
P AGN002 Agnosia 54 0.050
290
PRP016 Paraplegia 53 0.050
291
MYM001 Myoma 53 0.050
292
INF034 Infective Endocarditis 52 0.050
293
P SCK005 Sickle Cell Disease 50 0.050
294
RYN001 Raynaud Disease 49 0.050
295
STP011 Stapes Ankylosis with Broad Thumbs and Toes 48 0.050
296
CCN002 Cocaine Abuse 48 0.050
297
c BSL024 Basal Cell Carcinoma 1 47 0.050
298
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.050
299
HDN002 Head Injury 45 0.050
300
DVR002 Diverticulitis 44 0.050
301
CRT015 Carotid Artery Occlusion 44 0.050
302
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.050
303
TRP009 Triple X Syndrome 42 0.050
304
MYF001 Myofibroma 42 0.050
305
P CRN026 Corneal Edema 40 0.050
306
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 39 0.050
307
CRV045 Cervical Intraepithelial Neoplasia 39 0.050
308
c ACQ047 Acquired Methemoglobinemia 34 0.050
309
MBM001 Meibomian Cyst 34 0.050
310
BWN006 Bowen's Disease 32 0.050
311
IMM167 Immune Deficiency Disease 78 0.046
312
P RTN024 Retinoblastoma 72 0.046
313
P BRG001 Brugada Syndrome 70 0.046
314
P LYM118 Lymphoma 68 0.046
315
SKN019 Skin Melanoma 67 0.046
316
P LKM002 Leukemia 66 0.046
317
c FML001 Familial Atrial Fibrillation 66 0.046
318
P DRM053 Dermatitis, Atopic 66 0.046
319
CNN005 Connective Tissue Disease 66 0.046
320
c CHR684 Chronic Kidney Disease 66 0.046
321
APN008 Apnea, Obstructive Sleep 65 0.046
322
P DBT009 Diabetes Mellitus 64 0.046
323
P ENC004 Encephalitis 61 0.046
324
APP008 Appendicitis 60 0.046
325
P SLP005 Sleep Disorder 59 0.046
326
PLM033 Pulmonary Embolism 59 0.046
327
CHL067 Cholecystitis 58 0.046
328
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.046
329
ERY029 Erythermalgia, Primary 58 0.046
330
ERY003 Erythema Multiforme 57 0.046
331
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.046
332
GST050 Gastrointestinal System Disease 56 0.046
333
BRN004 Brain Edema 55 0.046
334
P SCK002 Sick Sinus Syndrome 55 0.046
335
INT007 Intermediate Coronary Syndrome 55 0.046
336
HMP005 Hemiplegia 54 0.046
337
SNS003 Sensory Peripheral Neuropathy 53 0.046
338
P RCT021 Rectum Cancer 53 0.046
339
c FML008 Familial Retinoblastoma 53 0.046
340
THR016 Thrombophlebitis 51 0.046
341
LNG031 Lung Benign Neoplasm 50 0.046
342
CCN001 Cocaine Dependence 48 0.046
343
SXL003 Sexual Disorder 48 0.046
344
LYM019 Lymphosarcoma 47 0.046
345
LNT004 Lentigines 46 0.046
346
AYM001 Ayme-Gripp Syndrome 46 0.046
347
P OCY003 Oocyte Maturation Defect 1 45 0.046
348
P HRN001 Horner's Syndrome 44 0.046
349
DRG024 Drug Allergy 43 0.046
350
TNS014 Tenosynovitis 43 0.046
351
ADP001 Adiposis Dolorosa 43 0.046
352
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.046
353
CRB086 Cerebral Aneurysms 40 0.046
354
NRV004 Nerve Compression Syndrome 38 0.046
355
IDP070 Idiopathic Scoliosis 37 0.046
356
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.046
357
c INT059 Internal Hemorrhoid 33 0.046
358
FNT004 Fainting 31 0.046
359
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.046
360
P LNG064 Lung Cancer Susceptibility 3 77 0.041
361
P PRK057 Parkinson Disease, Late-Onset 76 0.041
362
ADR007 Adrenoleukodystrophy 74 0.041
363
c ATR087 Atrial Standstill 1 74 0.041
364
BRN028 Brain Cancer 73 0.041
365
P GRF003 Graft-Versus-Host Disease 71 0.041
366
HMN044 Human Immunodeficiency Virus Type 1 71 0.041
367
P MYC084 Mycobacterium Tuberculosis 1 68 0.041
368
P HPT021 Hepatitis 67 0.041
369
c SML038 Small Cell Cancer of the Lung 65 0.041
370
PRT037 Pertussis 65 0.041
371
P DYS154 Dystonia 65 0.041
372
P ADN016 Adenocarcinoma 64 0.041
373
P GLM045 Glioma 63 0.041
374
PPL049 Papillon-Lefevre Syndrome 63 0.041
375
P LRS001 Larsen Syndrome 62 0.041
376
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.041
377
P PRP029 Porphyria 62 0.041
378
P PNC044 Pancreatitis 61 0.041
379
PRT013 Portal Hypertension 60 0.041
380
CRD132 Cardiac Conduction Defect 59 0.041
381
ADN018 Adenoma 58 0.041
382
P ALC033 Alcohol Use Disorder 58 0.041
383
c PRG126 Progressive Familial Heart Block 58 0.041
384
IRN002 Iron Metabolism Disease 57 0.041
385
DSS008 Disease of Mental Health 57 0.041
386
LMY014 Leiomyoma, Uterine 56 0.041
387
MCL006 Macular Retinal Edema 55 0.041
388
P VNS003 Venous Insufficiency 55 0.041
389
CLL003 Cellulitis 54 0.041
390
c CNT035 Central Nervous System Disease 54 0.041
391
THR013 Thoracic Outlet Syndrome 53 0.041
392
c FML191 Familial Long Qt Syndrome 53 0.041
393
NRT001 Neurotic Disorder 52 0.041
394
c LNG048 Long Qt Syndrome 3 52 0.041
395
ESP023 Esophageal Disease 52 0.041
396
IMP005 Impotence 52 0.041
397
P MSC003 Muscular Atrophy 52 0.041
398
TXC002 Toxic Encephalopathy 52 0.041
399
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.041
400
CHL056 Cheilitis 48 0.041
401
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 48 0.041
402
ASP007 Aspiration Pneumonia 48 0.041
403
DRG003 Drug Dependence 47 0.041
404
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.041
405
GLL048 Glial Tumor 45 0.041
406
PPL001 Papillary Adenoma 45 0.041
407
CNT017 Central Nervous System Origin Vertigo 44 0.041
408
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 43 0.041
409
URT037 Urethral Stricture 43 0.041
410
PLY068 Polysubstance Abuse 43 0.041
411
DNT014 Dental Pulp Disease 43 0.041
412
MCR011 Microinvasive Gastric Cancer 43 0.041
413
URT014 Ureterolithiasis 42 0.041
414
DFF003 Diffuse Scleroderma 42 0.041
415
49X006 49, Xxxxy Syndrome 41 0.041
416
SPN369 Spinal Disease 41 0.041
417
DNT006 Dental Pulp Necrosis 40 0.041
418
ACT093 Actinic Cheilitis 40 0.041
419
MNN017 Mononeuropathy 39 0.041
420
THR123 Thrombotic Microangiopathy 38 0.041
421
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.041
422
TRG003 Trigeminal Nerve Disease 36 0.041
424
P HPT023 Hepatocellular Carcinoma 100 0.035
425
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.035
426
P PNC035 Pancreatic Cancer 84 0.035
427
NRL016 Neural Tube Defects 82 0.035
428
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.035
429
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.035
430
c SPN225 Spondyloarthropathy 1 73 0.035
431
c HYP836 Hypercholesterolemia, Familial, 1 72 0.035
432
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.035
433
OTT002 Otitis Media 71 0.035
434
LYM133 Lymphoma, Hodgkin, Classic 69 0.035
435
ART016 Aortic Aneurysm 68 0.035
436
ACR008 Acrocallosal Syndrome 68 0.035
437
P LPR021 Leprosy 3 67 0.035
438
SVR097 Severe Cutaneous Adverse Reaction 67 0.035
439
PRT010 Parathyroid Carcinoma 66 0.035
440
P MCR115 Microvascular Complications of Diabetes 5 66 0.035
441
HYP056 Hypoglycemia 66 0.035
442
ATH013 Atherosclerosis Susceptibility 66 0.035
443
P ATS364 Autism 65 0.035
444
GST092 Gastroesophageal Reflux 65 0.035
445
CHY002 Chylomicron Retention Disease 64 0.035
446
CLF027 Cleft Palate, Isolated 64 0.035
447
GT001 Gout 63 0.035
448
P ANR048 Aniridia 1 63 0.035
449
INT146 Intervertebral Disc Disease 62 0.035
450
TMT001 Timothy Syndrome 62 0.035
451
c LCL006 Localized Scleroderma 62 0.035
452
HYP066 Hyperglycemia 61 0.035
453
P KDN017 Kidney Cancer 61 0.035
454
CHL068 Cholestasis 60 0.035
455
HPT019 Hepatic Encephalopathy 60 0.035
456
DCB001 Decubitus Ulcer 60 0.035
457
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.035
458
P BRN022 Bronchiectasis 59 0.035
459
HYD002 Hydronephrosis 59 0.035
460
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.035
461
GST045 Gastroenteritis 59 0.035
462
BRN002 Bronchiolitis 59 0.035
463
IGR001 Ige Responsiveness, Atopic 59 0.035
464
P FML052 Familial Cold Autoinflammatory Syndrome 59 0.035
465
P MTR012 Mitral Valve Disease 57 0.035
466
P OPT006 Optic Nerve Disease 57 0.035
467
CHN016 Cohen Syndrome 57 0.035
468
P RHN004 Rhinitis 57 0.035
469
GST033 Gestational Diabetes 57 0.035
470
P DRR001 Diarrhea 57 0.035
471
SPN041 Spinal Cord Disease 56 0.035
472
P DYS193 Dystonia 11, Myoclonic 56 0.035
473
P ALP008 Alopecia 56 0.035
474
RHM027 Rheumatic Disease 56 0.035
475
ALL006 Allergic Asthma 56 0.035
476
SYN007 Synovitis 55 0.035
477
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.035
478
LMB062 Limb Ischemia 55 0.035
479
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 0.035
480
P ART021 Arteriosclerosis 54 0.035
481
MYP139 Myopathy, Proximal, and Ophthalmoplegia 53 0.035
482
HRT012 Heart Valve Disease 53 0.035
483
GLS018 Glass Syndrome 53 0.035
484
ACR041 Acromelic Frontonasal Dysostosis 52 0.035
485
P HMR003 Hemorrhagic Disease 52 0.035
486
P RTN022 Retinal Vein Occlusion 52 0.035
487
DNT012 Dental Caries 51 0.035
488
BRX001 Bruxism 50 0.035
489
VLV047 Volvulus of Midgut 50 0.035
490
c XNT010 Xanthinuria, Type I 50 0.035
491
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.035
492
NTR046 Neutrophil Migration 50 0.035
493
LFT001 Left Bundle Branch Hemiblock 49 0.035
494
CLN045 Colonic Benign Neoplasm 49 0.035
495
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.035
496
ENT004 Enthesopathy 48 0.035
497
BLD044 Bladder Disease 48 0.035
498
DBT006 Diabetic Macular Edema 48 0.035
499
FCL012 Facial Paralysis 48 0.035
500
BNN003 Bone Inflammation Disease 48 0.035
501
P UTR058 Uterine Anomalies 48 0.035
502
OPD006 Opioid Addiction 48 0.035
503
SBS004 Substance Dependence 48 0.035
504
IRR003 Irritant Dermatitis 47 0.035
505
LMT001 Limited Scleroderma 47 0.035
506
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.035
507
VLV036 Vulvar Disease 46 0.035
508
KRT008 Keratopathy 46 0.035
509
c MLG068 Malignant Glioma 45 0.035
510
HRN026 Hernia, Hiatus 45 0.035
511
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.035
512
RTR001 Retrograde Amnesia 45 0.035
513
P BLP003 Blepharospasm 44 0.035
514
HPT004 Hepatic Coma 43 0.035
515
HMP009 Haemophilus Influenzae 42 0.035
516
SNL007 Senile Cataract 42 0.035
517
P SCL057 Scoliosis, Isolated 1 41 0.035
518
LMR001 Lemierre's Syndrome 40 0.035
519
ERY060 Erythroderma, Ichthyosiform, Congenital Reticular 39 0.035
520
MCC013 Mucocutaneous Ulceration, Chronic 39 0.035
521
c CHR682 Chronic Bilirubin Encephalopathy 38 0.035
522
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.035
523
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.035
524
P PRC031 Preeclampsia/eclampsia 1 37 0.035
525
PHM001 Phimosis 37 0.035
527
EPD005 Epidural Abscess 36 0.035
528
HRW001 Hair Whorl 36 0.035
529
MYT011 Myotonia 35 0.035
530
FXD003 Fixed Drug Eruption 35 0.035
531
PLN026 Pilonidal Sinus 35 0.035
532
HNS001 Hansen's Disease 34 0.035
534
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.035
535
CRV025 Cervical Incompetence 33 0.035
536
BNN005 Bunion 33 0.035
537
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.035
538
SPS016 Spasmodic Dysphonia 31 0.035
539
GST007 Gastric Dilatation 30 0.035
540
DSS002 Dissociative Amnesia 30 0.035
541
c CNT068 Central Pain Syndrome 29 0.035
542
MRL006 Meralgia Paraesthetica, Familial 29 0.035
543
TMP019 Temporomandibular Joint Anomaly 28 0.035
544
PRS120 Persistent Idiopathic Facial Pain 28 0.035
545
ERY066 Erythema Multiforme Major 28 0.035
546
BNG077 Benign Idiopathic Neonatal Seizures 26 0.035
547
c LNG052 Long Qt Syndrome 8 26 0.035
548
c CLR079 Colorectal Cancer 2 26 0.035
549
NRP027 Neuropathy, Painful 24 0.035
550
OBS635 Obsolete: Laryngeal Dyskinesia 23 0.035
551
P OVR042 Ovarian Cancer 89 0.029
552
P ALZ034 Alzheimer Disease 88 0.029
553
CYS001 Cystic Fibrosis 80 0.029
554
P RHM011 Rheumatoid Arthritis 80 0.029
555
c DLT002 Dilated Cardiomyopathy 79 0.029
556
c ART115 Aortic Valve Disease 1 75 0.029
557
GLB015 Glioblastoma Multiforme 75 0.029
558
CRH001 Crohn's Disease 74 0.029
559
SCH036 Scheie Syndrome 71 0.029
560
c HPT073 Hepatitis C Virus 70 0.029
561
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.029
562
c GLY008 Glycogen Storage Disease Ii 70 0.029
563
P PLM037 Pulmonary Hypertension 68 0.029
564
P INF038 Influenza 68 0.029
565
P THR014 Thrombocytopenia 68 0.029
566
CRB037 Cerebral Palsy 68 0.029
567
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.029
568
KRT019 Keratitis, Hereditary 67 0.029
569
P DMN002 Dementia 67 0.029
570
GRG001 Greig Cephalopolysyndactyly Syndrome 67 0.029
571
OST159 Osteogenic Sarcoma 66 0.029
572
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 66 0.029
573
P HYD006 Hydrocephalus 65 0.029
574
P ART005 Arteriovenous Malformation 65 0.029
575
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.029
576
P CHR071 Charcot-Marie-Tooth Disease 64 0.029
577
OST017 Osteomyelitis 64 0.029
578
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.029
579
KHL003 Kohlschutter-Tonz Syndrome 64 0.029
580
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.029
581
LSH001 Leishmaniasis 63 0.029
582
P ORT004 Orthostatic Intolerance 63 0.029
583
c HPT001 Hepatitis C 63 0.029
584
KRN002 Kearns-Sayre Syndrome 63 0.029
585
LPD008 Lipid Metabolism Disorder 62 0.029
586
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.029
587
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 62 0.029
588
CLT003 Colitis 62 0.029
589
P CTS001 Cutis Laxa 62 0.029
590
c GLC092 Glaucoma, Primary Open Angle 62 0.029
591
PSR001 Psoriatic Arthritis 62 0.029
592
c ATM011 Autoimmune Hepatitis 62 0.029
593
CTN007 Cutaneous Leishmaniasis 61 0.029
594
P PRM006 Primary Biliary Cirrhosis 61 0.029
595
CHR066 Chronic Fatigue Syndrome 61 0.029
596
P MVM001 Movement Disease 61 0.029
597
P HMN010 Hemangioma 61 0.029
598
INT002 Intermittent Claudication 61 0.029
599
c BRN108 Branchiootic Syndrome 1 61 0.029
600
ATM095 Autoimmune Disease 61 0.029
601
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.029
602
DPH001 Diphtheria 60 0.029
603
P ALP009 Alopecia Areata 60 0.029
604
MRT001 Muir-Torre Syndrome 60 0.029
605
CHC001 Chickenpox 60 0.029
606
ETN001 Eating Disorder 59 0.029
607
P GLY013 Glycogen Storage Disease 59 0.029
608
SPP011 Suppression of Tumorigenicity 12 59 0.029
609
PRT058 Pure Autonomic Failure 59 0.029
610
c HPT016 Hepatitis B 59 0.029
611
P TRC086 Trichohepatoenteric Syndrome 1 59 0.029
612
P BRS044 Breast Adenocarcinoma 59 0.029
613
PPT005 Peptic Ulcer Disease 58 0.029
614
P BCL017 B-Cell Lymphoma 58 0.029
615
P CND004 Candidiasis 57 0.029
616
SPT004 Septic Arthritis 57 0.029
617
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.029
618
P EHL001 Ehlers-Danlos Syndrome 57 0.029
619
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 57 0.029
620
c CHR417 Chronic Graft Versus Host Disease 56 0.029
621
P EPD003 Epidermolysis Bullosa Simplex 56 0.029
622
ORL005 Oral Candidiasis 56 0.029
623
CMR002 Coumarin Resistance 56 0.029
624
KRT071 Keratosis, Seborrheic 56 0.029
625
ACS001 Acoustic Neuroma 56 0.029
626
BRD001 Brody Myopathy 55 0.029
627
CHL014 Cholera 55 0.029
628
NRG002 Neurogenic Bladder 54 0.029
629
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.029
630
P LCH002 Lichen Planus 54 0.029
631
P RST001 Restless Legs Syndrome 54 0.029
632
P SPN052 Spondyloarthropathy 54 0.029
633
P EPD016 Epidermolysis Bullosa 53 0.029
634
NRT004 Neuritis 53 0.029
635
MMM001 Mammary Paget's Disease 53 0.029
636
BRN038 Bronchial Disease 53 0.029
637
HMT008 Hematuria, Benign Familial 53 0.029
638
P THY032 Thyroiditis 53 0.029
639
PRP080 Peripheral Artery Disease 53 0.029
640
EXP004 Exophthalmos 52 0.029
641
P INT068 Intestinal Disease 52 0.029
642
SPN051 Spondylitis 52 0.029
643
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.029
644
MTN003 Motion Sickness 52 0.029
645
c VRL010 Viral Hepatitis 51 0.029
646
TLN003 Telangiectasis 51 0.029
647
HND002 Hand, Foot and Mouth Disease 51 0.029
648
c ACT134 Acute Liver Failure 51 0.029
649
c BRG005 Brugada Syndrome 1 50 0.029
650
ADT003 Auditory System Disease 50 0.029
651
PTT041 Pituitary Stalk Interruption Syndrome 50 0.029
652
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.029
653
CLR109 Colorectal Adenocarcinoma 50 0.029
654
P TMP001 Temporal Lobe Epilepsy 50 0.029
655
P CHL066 Cholangitis 50 0.029
656
P MGR003 Migraine with Aura 50 0.029
657
FSC004 Fasciitis 50 0.029
658
P OVR082 Overgrowth Syndrome 50 0.029
659
P OTS001 Otosclerosis 50 0.029
660
P CTN015 Cutaneous T Cell Lymphoma 49 0.029
661
HYP006 Hypertensive Heart Disease 49 0.029
662
LRN003 Learning Disability 49 0.029
663
P OPN001 Open-Angle Glaucoma 49 0.029
664
BLL003 Bell's Palsy 49 0.029
665
SKN013 Skin Benign Neoplasm 49 0.029
666
URM002 Uremia 49 0.029
667
SNT005 Sinoatrial Node Disease 49 0.029
668
P CMP008 Compartment Syndrome 48 0.029
669
DNT045 Dental Anomalies and Short Stature 48 0.029
670
c DSB006 Desbuquois Dysplasia 1 48 0.029
671
CRD137 Cardiogenic Shock 48 0.029
672
P KRT005 Keratoacanthoma 48 0.029
673
KHN001 Kuhnt-Junius Degeneration 48 0.029
674
DGN001 Degenerative Disc Disease 48 0.029
675
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 48 0.029
676
RGH001 Right Bundle Branch Block 47 0.029
677
ATN005 Autonomic Dysfunction 47 0.029
678
PRC003 Proctitis 47 0.029
679
UMB002 Umbilical Hernia 47 0.029
680
MLT006 Multidrug-Resistant Tuberculosis 47 0.029
681
HRD005 Hard Palate Cancer 46 0.029
682
TTH006 Tooth Disease 46 0.029
683
PGT003 Paget Disease, Extramammary 46 0.029
684
SPN020 Spondylosis 46 0.029
685
URT010 Ureteral Obstruction 46 0.029
686
PRM057 Paramyotonia Congenita of Von Eulenburg 46 0.029
687
c SBC007 Subacute Thyroiditis 46 0.029
688
c CHR048 Chronic Rhinitis 46 0.029
689
PRT030 Parathyroid Gland Disease 45 0.029
690
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.029
691
GRN007 Granuloma Annulare 45 0.029
692
ASP004 Asphyxia Neonatorum 45 0.029
693
LRY029 Laryngomalacia 45 0.029
694
SPR005 Superficial Basal Cell Carcinoma 45 0.029
695
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 45 0.029
696
PTT037 Pituitary Tumors 44 0.029
697
CRB004 Cerebral Artery Occlusion 44 0.029
698
PNC085 Penicillin Allergy 44 0.029
699
P BCT020 Bacteremia 2 44 0.029
700
MRG013 Mirage Syndrome 44 0.029
701
IMM064 Immunodeficiency, Common Variable, 10 44 0.029
702
c PCH010 Pachyonychia Congenita 3 43 0.029
703
SKN005 Skin Atrophy 43 0.029
704
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.029
705
c HRD173 Hereditary Late-Onset Parkinson Disease 43 0.029
706
HYP457 Hypertrophic Scars 43 0.029
707
ARC002 Arachnoiditis 42 0.029
708
URT031 Ureteral Disease 42 0.029
709
ANX004 Anoxia 42 0.029
710
BP1002 Bap1 Tumor Predisposition Syndrome 41 0.029
711
P CRN035 Cranial Nerve Palsy 41 0.029
712
P KLZ004 Kala-Azar 1 41 0.029
713
MRP001 Morphine Dependence 41 0.029
714
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.029
715
MTR007 Motor Peripheral Neuropathy 40 0.029
716
ANG049 Angioedema Induced by Ace Inhibitors 40 0.029
717
P TRC031 Trichorhinophalangeal Syndrome 40 0.029
718
HYP264 Hypertonia 38 0.029
719
P HMF004 Hemifacial Spasm 38 0.029
720
c CHR020 Chronic Interstitial Cystitis 37 0.029
721
c LPR022 Leprosy 2 37 0.029
722
SPN354 Spinal Arachnoiditis 36 0.029
723
CNT018 Central Nervous System Leukemia 35 0.029
724
PLM028 Pulmonary Coin Lesion 35 0.029
725
c RST012 Restless Legs Syndrome 1 34 0.029
726
c HMF011 Hemifacial Spasm, Familial 33 0.029
727
SCR039 Scorpion Envenomation 33 0.029
728
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.029
729
NRD001 Neurodermatitis 32 0.029
730
INF009 Inflammatory Spondylopathy 32 0.029
731
PLN007 Plantar Fasciitis 31 0.029
732
PDN001 Pudendal Neuralgia 31 0.029
733
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 31 0.029
734
PLY150 Polykaryocytosis Inducer 31 0.029
735
INT042 Internuclear Ophthalmoplegia 30 0.029
736
HMC012 Hemicrania Continua 28 0.029
737
VLV021 Vulval Paget's Disease 28 0.029
738
FCL007 Facial Neuralgia 28 0.029
739
ANS018 Anismus 27 0.029
740
PTL003 Patellar Tendinitis 27 0.029
741
DVR001 Diverticulitis of Colon 26 0.029
742
TRG006 Trigger Thumb 23 0.029
743
SNC001 Sunct Headache 23 0.029
744
CRN309 Cranial Neuralgia 22 0.029
745
HML018 Homologous Wasting Disease 22 0.029
746
DPB002 Deep Brain Stimulation for Movement Disorders 16 0.029
747
ESP021 Esophageal Cancer 90 0.020
748
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.020
749
c SYS001 Systemic Lupus Erythematosus 86 0.020
750
MLR004 Malaria 80 0.020
751
CNN003 Conn's Syndrome 79 0.020
752
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.020
753
END057 Endometrial Cancer 74 0.020
754
c HMC039 Hemochromatosis, Type 1 74 0.020
755
ACR006 Aceruloplasminemia 73 0.020
756
ULC004 Ulcerative Colitis 73 0.020
757
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.020
758
ACR007 Acromegaly 71 0.020
759
P SRC025 Sarcoidosis 1 70 0.020
760
WLS001 Wilson Disease 70 0.020
761
SMT004 Smith-Lemli-Opitz Syndrome 69 0.020
762
P LKM062 Leukemia, Acute Lymphoblastic 68 0.020
763
NVS017 Nevus, Epidermal 68 0.020
764
P MYS003 Myasthenia Gravis 68 0.020
765
P MJR001 Major Depressive Disorder 68 0.020
766
ALL003 Allergic Rhinitis 67 0.020
767
P NSP012 Nasopharyngeal Carcinoma 67 0.020
768
P ANG001 Angelman Syndrome 67 0.020
769
PSY004 Psychotic Disorder 67 0.020
770
FML089 Familial Thoracic Aortic Aneurysm and Dissection 66 0.020
771
P HYP061 Hypertrophic Cardiomyopathy 66 0.020
772
FCT007 Factor Vii Deficiency 66 0.020
773
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.020
774
P MSC005 Muscular Dystrophy 66 0.020
775
P HYP098 Hypereosinophilic Syndrome 66 0.020
776
LNG039 Lung Squamous Cell Carcinoma 65 0.020
777
P HRP006 Herpes Simplex 65 0.020
778
DMN031 Dementia, Lewy Body 65 0.020
779
BRR014 Barrett Esophagus 64 0.020
780
GRN037 Granulomatosis with Polyangiitis 64 0.020
781
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.020
782
P MYP004 Myopathy 64 0.020
783
P MTR014 Motor Neuron Disease 64 0.020
784
NRF007 Neurofibroma 64 0.020
785
P GCH001 Gaucher's Disease 64 0.020
786
CLN015 Colon Adenocarcinoma 63 0.020
787
PRP083 Porphyria, Acute Intermittent 63 0.020
788
c ART101 Aortic Valve Disease 2 63 0.020
789
IDP011 Idiopathic Interstitial Pneumonia 63 0.020
790
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.020
791
DGR001 Digeorge Syndrome 63 0.020
792
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.020
793
P MST009 Mastocytosis 63 0.020
794
NRM005 Neuromuscular Disease 63 0.020
795
ART002 Arts Syndrome 63 0.020
796
P NTR004 Neutropenia 63 0.020
797
P NPH012 Nephrotic Syndrome 63 0.020
798
ANR007 Anorexia Nervosa 63 0.020
799
P HYP069 Hyperparathyroidism 62 0.020
800
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.020
801
P PSR002 Psoriasis 62 0.020
802
TRN015 Transient Cerebral Ischemia 62 0.020
803
P ESP024 Esophagitis 62 0.020
804
HMT002 Hematologic Cancer 62 0.020
805
P PLM036 Pulmonary Fibrosis 61 0.020
806
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.020
807
P DRM010 Dermatomyositis 61 0.020
808
OSS012 Osseous Heteroplasia, Progressive 61 0.020
809
P HYP750 Hypertriglyceridemia, Familial 61 0.020
810
FTT001 Fatty Liver Disease 61 0.020
811
P LPS004 Lupus Erythematosus 61 0.020
812
SDD001 Sudden Infant Death Syndrome 61 0.020
813
VRL011 Viral Infectious Disease 61 0.020
814
RHM001 Rheumatic Fever 61 0.020
815
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 61 0.020
816
ERL001 Early Myoclonic Encephalopathy 61 0.020
817
MSL001 Measles 61 0.020
818
NRL005 Neurilemmoma 60 0.020
819
P NRM001 Neuromyelitis Optica 60 0.020
820
ACN002 Acanthosis Nigricans 60 0.020
821
P VNT002 Ventricular Septal Defect 60 0.020
822
ORL011 Oral Cancer 60 0.020
823
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.020
824
INT066 Interstitial Lung Disease 59 0.020
825
P MYC008 Myocarditis 59 0.020
826
c VSC019 Vesicoureteral Reflux 1 59 0.020
827
MXD005 Mixed Connective Tissue Disease 59 0.020
828
GNG013 Gingivitis 59 0.020
829
c ACT027 Acute Pancreatitis 59 0.020
830
c LPM012 Lipomatosis, Multiple 59 0.020
831
P SYP003 Syphilis 59 0.020
832
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.020
833
CHL123 Chlamydia 59 0.020
834
c BNG091 Benign Chronic Pemphigus 59 0.020
835
HLC007 Helicobacter Pylori Infection 59 0.020
836
TTZ003 Tietz Albinism-Deafness Syndrome 58 0.020
837
P RBL001 Rubella 58 0.020
838
c LNG047 Long Qt Syndrome 2 58 0.020
839
P INT070 Intestinal Obstruction 58 0.020
840
PRL032 Perlman Syndrome 58 0.020
841
P DST002 Distal Arthrogryposis 58 0.020
842
EYD002 Eye Disease 58 0.020
843
BRS051 Breast Disease 58 0.020
844
EXT034 Extrinsic Allergic Alveolitis 58 0.020
845
PMP006 Pemphigus Vulgaris, Familial 58 0.020
846
BRG013 Buerger Disease 57 0.020
847
c CHL119 Cholangitis, Primary Sclerosing 57 0.020
848
PLM070 Pulmonic Stenosis 57 0.020
849
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.020
850
P MMP001 Mumps 57 0.020
851
P PLY041 Polymyositis 57 0.020
852
P BNC003 Bone Cancer 57 0.020
853
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.020
854
P UVT001 Uveitis 57 0.020
855
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 57 0.020
856
APH001 Aphthous Stomatitis 57 0.020
857
APH002 Aphasia 57 0.020
858
LNN001 Lennox-Gastaut Syndrome 57 0.020
859
P GLM007 Glomerulonephritis 57 0.020
860
P SJG008 Sjogren Syndrome 56 0.020
861
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.020
862
P FBR017 Fibrosarcoma 56 0.020
863
P OPT009 Optic Neuritis 56 0.020
864
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.020
865
P MLN007 Male Infertility 56 0.020
866
SKN022 Skin Squamous Cell Carcinoma 56 0.020
867
P PLY011 Polycystic Ovary Syndrome 56 0.020
868
FDB001 Foodborne Botulism 56 0.020
869
P MYS005 Myositis 56 0.020
870
BRN012 Bronchiolitis Obliterans 56 0.020
871
P GST044 Gastritis 55 0.020
872
P HYP024 Hypoparathyroidism 55 0.020
873
PRP030 Purpura 55 0.020
874
c SVR001 Severe Acute Respiratory Syndrome 55 0.020
875
GRN034 Grange Syndrome 55 0.020
876
P MYT023 Myotonia Congenita 55 0.020
877
c FML035 Familial Hyperlipidemia 55 0.020
878
ACT058 Active Peptic Ulcer Disease 55 0.020
879
c MYP132 Myopathy, Congenital 55 0.020
880
ANS023 Anus, Imperforate 55 0.020
881
AND020 Androgen Insensitivity, Partial 55 0.020
882
VSC003 Visceral Leishmaniasis 55 0.020
883
TNG003 Tongue Cancer 55 0.020
884
P PMP001 Pemphigus 55 0.020
885
VGN023 Vaginitis 55 0.020
886
P LYM031 Lymphocytic Leukemia 55 0.020
887
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.020
888
HYP060 Hyperinsulinism 54 0.020
889
CRT017 Cartilage Disease 54 0.020
890
PPL022 Papilloma 54 0.020
891
VLC001 Velocardiofacial Syndrome 54 0.020
892
P ANG015 Angioedema 54 0.020
893
GLC003 Glucose Intolerance 54 0.020
894
FCL014 Focal Epilepsy 54 0.020
895
ORP003 Oropharynx Cancer 54 0.020
896
HST011 Histoplasmosis 54 0.020
897
c PRD040 Periodontitis, Chronic 54 0.020
898
P ESP035 Esophagitis, Eosinophilic, 1 54 0.020
899
P LRY044 Larynx Cancer 54 0.020
900
PTT009 Pituitary Gland Disease 54 0.020
901
AMN001 Amenorrhea 54 0.020
902
GST037 Gastroparesis 53 0.020
903
PRX015 Paroxysmal Extreme Pain Disorder 53 0.020
904
CHR100 Chronic Ulcer of Skin 53 0.020
905
P LTR001 Lateral Sclerosis 53 0.020
906
RHM028 Rheumatic Heart Disease 53 0.020
907
MST005 Mastitis 53 0.020
908
LYM004 Lymphoid Interstitial Pneumonia 53 0.020
909
P LYM025 Lymphedema 53 0.020
910
OST016 Osteochondrosis 53 0.020
911
P OVR049 Ovarian Disease 53 0.020
912
GST023 Gastric Ulcer 53 0.020
913
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 53 0.020
914
P RTN018 Retinal Disease 52 0.020
915
c MCR113 Microvascular Complications of Diabetes 3 52 0.020
916
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.020
917
BCT002 Bacterial Vaginosis 52 0.020
918
PST011 Pustulosis of Palm and Sole 52 0.020
919
FML037 Female Breast Cancer 52 0.020
920
P INS002 in Situ Carcinoma 52 0.020
921
c PSR017 Psoriasis 2 52 0.020
922
P LRY019 Laryngitis 51 0.020
923
CHL122 Cholesteatoma of Middle Ear 51 0.020
924
PPT001 Peptic Esophagitis 51 0.020
925
GNG012 Gingival Overgrowth 51 0.020
926
CRY001 Cryptogenic Organizing Pneumonia 51 0.020
927
MYL020 Myelomeningocele 51 0.020
928
SPP010 Suppressor of Tumorigenicity 3 51 0.020
929
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.020
930
VLV011 Vulvovaginal Candidiasis 51 0.020
931
ESP002 Esophageal Varix 51 0.020
932
BWN001 Bowen-Conradi Syndrome 51 0.020
933
P HYP040 Hypospadias 51 0.020
934
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.020
935
NNL006 Non-Alcoholic Steatohepatitis 51 0.020
936
GSG001 Gas Gangrene 50 0.020
937
AZS001 Azoospermia 50 0.020
938
HRT011 Heart Septal Defect 50 0.020
939
RTN003 Retinal Ischemia 50 0.020
940
P HYP077 Hypertrichosis 50 0.020
941
HPT014 Hepatorenal Syndrome 50 0.020
942
PST021 Postpartum Depression 50 0.020
943
SPS003 Spastic Diplegia 50 0.020
944
IRD001 Iridocyclitis 50 0.020
945
SLD003 Sialadenitis 50 0.020
946
c PYR010 Peyronie's Disease 50 0.020
947
P BRT029 Brittle Cornea Syndrome 2 50 0.020
948
P AGG001 Aggressive Periodontitis 50 0.020
949
PRT018 Portal Vein Thrombosis 50 0.020
950
c INF145 Infantile Liver Failure Syndrome 1 50 0.020
951
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.020
952
CRT013 Carotid Stenosis 50 0.020
953
c CNG216 Congenital Hydrocephalus 50 0.020
954
LPR001 Lepromatous Leprosy 50 0.020
955
RSP006 Respiratory System Disease 50 0.020
956
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.020
957
CRN030 Coronary Stenosis 50 0.020
958
P CRN276 Corneal Endothelial Dystrophy 50 0.020
959
KRT001 Keratoconjunctivitis Sicca 50 0.020
960
VGN020 Vaginal Disease 50 0.020
961
P KRT007 Keratoconus 49 0.020
962
BRN009 Burning Mouth Syndrome 49 0.020
963
c CNT016 Central Retinal Vein Occlusion 49 0.020
964
BLP005 Blepharitis 49 0.020
965
PLR007 Pleural Empyema 49 0.020
966
PLM041 Pulmonary Valve Stenosis 49 0.020
967
c SVR005 Severe Pre-Eclampsia 49 0.020
968
c PSR023 Psoriasis 1 49 0.020
969
BLS002 Blastomycosis 49 0.020
970
c CHR431 Chronic Venous Insufficiency 49 0.020
971
c DYS119 Dystonia 9 49 0.020
972
P RNV001 Renovascular Hypertension 49 0.020
973
GST049 Gastrointestinal System Cancer 49 0.020
974
SPN019 Spondylolisthesis 49 0.020
975
BNR002 Bone Resorption Disease 48 0.020
976
BCT004 Bacteriuria 48 0.020
977
VTM033 Vitamin K Deficiency Bleeding 48 0.020
978
SBP001 Subependymal Giant Cell Astrocytoma 48 0.020
979
P OBS001 Obstructive Jaundice 48 0.020
980
HYP043 Hyperandrogenism 48 0.020
981
P DPY001 Dupuytren Contracture 48 0.020
982
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 48 0.020
983
P BRS053 Breast Fibroadenoma 48 0.020
984
END062 Endometrial Hyperplasia 48 0.020
985
CLC006 Calcinosis 48 0.020
986
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 48 0.020
987
P MGR001 Migraine Without Aura 48 0.020
988
RTN020 Retinal Vascular Disease 48 0.020
989
PCT003 Pectus Excavatum 48 0.020
990
c SHR030 Short Qt Syndrome 48 0.020
991
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.020
992
PRP007 Priapism 48 0.020
993
HLX001 Helix Syndrome 47 0.020
994
ANV001 Anovulation 47 0.020
995
DRY001 Dry Eye Syndrome 47 0.020
996
P CRN028 Corneal Ulcer 47 0.020
997
AST006 Astigmatism 47 0.020
998
TST044 Testicular Torsion 47 0.020
999
PPL002 Papillary Carcinoma 47 0.020
1000
c MCR120 Microvascular Complications of Diabetes 7 47 0.020
1001
P SCL009 Sclerosing Cholangitis 47 0.020
1002
P CRC039 Coarctation of Aorta 47 0.020
1003
ANL022 Anal Fistula 47 0.020
1004
MCC002 Mucocutaneous Leishmaniasis 47 0.020
1005
EXS001 Exostosis 46 0.020
1006
ANH002 Anhidrosis 46 0.020
1007
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 46 0.020
1008
PRP017 Periapical Periodontitis 46 0.020
1009
MYT030 Myotonia, Potassium-Aggravated 46 0.020
1010
MDD010 Middle Ear Disease 46 0.020
1011
c LYM145 Lymphatic Malformation 5 46 0.020
1012
P CRN025 Corneal Dystrophy 45 0.020
1013
GST071 Gastrointestinal Carcinoma 45 0.020
1014
STS002 Situs Inversus 45 0.020
1015
c TRC022 Tricuspid Valve Insufficiency 45 0.020
1016
c EPD030 Epidermolysis Bullosa Simplex, Localized 45 0.020
1017
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.020
1018
RTR008 Root Resorption 45 0.020
1019
P BNG032 Benign Mesothelioma 45 0.020
1020
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.020
1021
ACT003 Acute Kidney Tubular Necrosis 45 0.020
1022
HRP001 Herpangina 45 0.020
1023
P MGL013 Megalencephaly 45 0.020
1024
THR099 Third-Degree Atrioventricular Block 45 0.020
1026
NNS002 Nonspecific Interstitial Pneumonia 45 0.020
1027
INT071 Intestinal Perforation 45 0.020
1028
ACT029 Acute Interstitial Pneumonia 44 0.020
1029
LRY022 Laryngoonychocutaneous Syndrome 44 0.020
1030
RTN021 Retinal Vascular Occlusion 44 0.020
1031
ESN004 Eosinophilic Gastritis 44 0.020
1032
GNG003 Gingival Recession 44 0.020
1033
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 0.020
1034
TNG009 Tongue Squamous Cell Carcinoma 44 0.020
1035
PRS042 Prostate Disease 44 0.020
1036
LMY003 Leiomyomatosis 43 0.020
1037
ANS012 Anus Disease 43 0.020
1038
c PRM038 Primary Agammaglobulinemia 43 0.020
1039
ALK024 Alkuraya-Kucinskas Syndrome 43 0.020
1040
LTX001 Latex Allergy 43 0.020
1041
ORL015 Oral Squamous Cell Carcinoma 43 0.020
1042
GRW007 Growth Hormone Deficiency 43 0.020
1043
EST005 Esotropia 43 0.020
1044
c SRC023 Sarcoidosis 2 43 0.020
1045
BLD161 Blood Group, Globoside System 42 0.020
1046
SQM002 Squamous Cell Papilloma 42 0.020
1047
ASP008 Aspiration Pneumonitis 42 0.020
1048
NDL009 Nodular Basal Cell Carcinoma 42 0.020
1049
XRP001 Xerophthalmia 42 0.020
1050
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.020
1051
MCR103 Microtia 42 0.020
1052
c PRG011 Progressive Myoclonus Epilepsy 42 0.020
1053
LRY017 Laryngeal Disease 42 0.020
1054
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.020
1055
SPC005 Speech Disorder 42 0.020
1056
FTL021 Fetal Macrosomia 42 0.020
1057
GST020 Gastric Antral Vascular Ectasia 41 0.020
1058
NSP002 Nasopharyngitis 41 0.020
1059
c NLD016 Nail Disorder, Nonsyndromic Congenital, 10 41 0.020
1060
VLV010 Vulvovaginitis 41 0.020
1061
SPN029 Spondylolysis 41 0.020
1062
RST023 Resting Heart Rate, Variation in 41 0.020
1063
FSC002 Fascioliasis 41 0.020
1064
c MCR130 Microvascular Complications of Diabetes 6 41 0.020
1065
c MCR133 Microvascular Complications of Diabetes 4 41 0.020
1066
MMM006 Mammographic Density 41 0.020
1067
PHB001 Phobic Disorder 41 0.020
1068
LCR013 Lacrimal Duct Defect 41 0.020
1069
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.020
1070
c MCR112 Microvascular Complications of Diabetes 2 41 0.020
1071
P RRT020 Rare Tumor 41 0.020
1072
FRM003 Farmer's Lung 40 0.020
1073
JWD001 Jawad Syndrome 40 0.020
1074
SLT009 Solitary Bone Cyst 40 0.020
1075
SPR126 Superior Semicircular Canal Dehiscence 40 0.020
1076
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 40 0.020
1077
c PLM022 Pulmonary Valve Insufficiency 40 0.020
1078
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.020
1079
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.020
1080
PLM005 Pleomorphic Lipoma 39 0.020
1081
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 39 0.020
1082
c ART028 Aortic Aneurysm, Familial Thoracic 4 39 0.020
1083
P OTT001 Otitis Externa 39 0.020
1084
ADP007 Adie Pupil 39 0.020
1085
PPL035 Papillary Thyroid Microcarcinoma 39 0.020
1086
c EPL026 Epileptic Encephalopathy, Early Infantile, 3 39 0.020