Search results for Analgesics, Non-Narcotic

1662 hits were found for Analgesics, Non-Narcotic

# Family MCID Name MIFTS Score
1
PNG002 Pain Agnosia 51 0.441
2
P CHR345 Chronic Pain 44 0.296
3
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.261
4
c PNS012 Paine Syndrome 61 0.261
5
OST012 Osteoarthritis 78 0.156
6
P HDC001 Headache 57 0.150
7
CNS004 Constipation 58 0.132
8
c MGR028 Migraine with or Without Aura 1 67 0.125
9
DRG003 Drug Dependence 47 0.102
10
INT067 Interstitial Nephritis 48 0.098
11
GRN017 Granulocytopenia 44 0.097
12
WTH001 Withdrawal Disorder 48 0.089
13
DBT010 Diabetic Neuropathy 54 0.089
14
c ACT071 Acute Kidney Failure 60 0.088
15
END086 End Stage Renal Disease 51 0.088
16
APP008 Appendicitis 61 0.087
17
ING001 Inguinal Hernia 60 0.086
18
PST053 Postherpetic Neuralgia 40 0.085
19
IRR002 Irritable Bowel Syndrome 65 0.085
20
c RHB024 Rhabdomyosarcoma 2 67 0.083
21
P SBS003 Substance Abuse 55 0.080
22
NPH009 Nephrolithiasis 55 0.080
23
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.079
24
TRG002 Trigeminal Neuralgia 60 0.079
25
GST023 Gastric Ulcer 53 0.079
26
P BNC003 Bone Cancer 58 0.078
27
c ACT068 Acute Cystitis 63 0.077
28
HYP056 Hypoglycemia 66 0.075
29
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.073
30
P PRD008 Periodontitis 64 0.072
31
P BRS047 Breast Cancer 97 0.071
32
P SCK005 Sickle Cell Disease 50 0.071
33
ILS001 Ileus 51 0.070
34
PLP001 Pulpitis 49 0.070
35
c MCR129 Microvascular Complications of Diabetes 1 66 0.068
36
SPN186 Spinal Cord Injury 60 0.067
37
CMP010 Complex Regional Pain Syndrome 58 0.067
38
P PLY019 Polyneuropathy 56 0.067
39
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.067
40
PNM008 Pneumothorax 56 0.066
41
MCS002 Mucositis 56 0.066
42
SYN007 Synovitis 54 0.066
43
AMN003 Amnestic Disorder 54 0.066
44
PLC002 Plica Syndrome 36 0.066
45
HYP266 Hypoxia 57 0.065
46
P ART023 Arthropathy 62 0.065
47
PPT005 Peptic Ulcer Disease 59 0.065
48
P NPH012 Nephrotic Syndrome 60 0.064
49
P OVR042 Ovarian Cancer 88 0.064
50
PRT036 Peritonitis 64 0.064
51
HRP004 Herpes Zoster 60 0.064
52
P GLM007 Glomerulonephritis 57 0.064
53
P PNC044 Pancreatitis 61 0.063
54
CRP001 Carpal Tunnel Syndrome 67 0.062
55
c ACT134 Acute Liver Failure 56 0.062
56
PNM010 Pneumothorax, Primary Spontaneous 60 0.062
57
P TRM003 Tremor 54 0.062
58
MTB004 Metabolic Acidosis 50 0.061
59
P BLD134 Bladder Cancer 79 0.061
60
c ACT027 Acute Pancreatitis 60 0.061
61
P PNM007 Pneumonia 68 0.060
62
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.060
63
47X002 47,xyy 49 0.060
65
P OST002 Osteoporosis 74 0.059
66
GT001 Gout 64 0.059
67
c ACT075 Acute Myocardial Infarction 57 0.059
68
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.059
69
P APL001 Aplastic Anemia 74 0.058
70
P PNC035 Pancreatic Cancer 84 0.058
71
ADL002 Adult Syndrome 70 0.058
72
P INT143 Interstitial Cystitis 61 0.058
73
P CTR002 Cataract 60 0.058
74
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.058
75
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.058
76
CNN005 Connective Tissue Disease 68 0.057
77
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.056
78
VSL002 Visual Epilepsy 59 0.056
79
MCN017 Meconium Ileus 52 0.056
80
DBT002 Diabetic Autonomic Neuropathy 41 0.056
81
GLB015 Glioblastoma Multiforme 75 0.056
82
P CLR023 Colorectal Cancer 99 0.055
83
DWN001 Down Syndrome 70 0.055
84
ANG054 Angina Pectoris 66 0.055
85
DRM006 Dermatitis 61 0.055
86
SPN051 Spondylitis 51 0.055
87
P HMR005 Hemorrhoid 46 0.055
88
URL001 Urolithiasis 45 0.055
89
c PRM038 Primary Agammaglobulinemia 44 0.055
90
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.055
91
INF009 Inflammatory Spondylopathy 31 0.055
92
RYS001 Reye Syndrome 51 0.055
93
P NRV007 Nervous System Disease 66 0.054
94
PRT037 Pertussis 65 0.054
95
P SCL018 Scoliosis 60 0.054
96
P CRD246 Cardiovascular System Disease 57 0.054
97
RDC002 Radiculopathy 50 0.054
98
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.054
99
CYT002 Cytokine Deficiency 42 0.054
100
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.054
101
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.054
102
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.054
103
MSL001 Measles 62 0.053
104
BRN004 Brain Edema 56 0.053
105
P PRS040 Prostate Cancer 97 0.053
106
P ALZ034 Alzheimer Disease 88 0.053
107
MDD011 Mood Disorder 62 0.053
108
P KDN017 Kidney Cancer 60 0.053
109
ISC004 Ischemia 58 0.053
110
P HYP040 Hypospadias 51 0.053
111
OVR094 Ovarian Epithelial Cancer 38 0.053
112
P GST053 Gastric Cancer 83 0.051
113
SCK003 Sickle Cell Anemia 74 0.051
114
OTT002 Otitis Media 72 0.051
115
HMN044 Human Immunodeficiency Virus Type 1 71 0.051
116
P MJR001 Major Depressive Disorder 68 0.051
117
OST159 Osteogenic Sarcoma 66 0.051
118
P MCR115 Microvascular Complications of Diabetes 5 66 0.051
119
P END044 Endometriosis 63 0.051
120
LPP008 Lipoprotein Quantitative Trait Locus 62 0.051
121
P CYS018 Cystitis 59 0.051
122
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.051
123
P GLL020 Gallbladder Disease 57 0.051
124
CMM005 Common Cold 57 0.051
125
P STR020 Strabismus 55 0.051
126
CLF001 Cleft Lip 53 0.051
127
PST021 Postpartum Depression 50 0.051
128
c MCR120 Microvascular Complications of Diabetes 7 47 0.051
129
IDP070 Idiopathic Scoliosis 42 0.051
130
MCH006 Mechanical Strabismus 42 0.051
131
CHL068 Cholestasis 61 0.051
132
DSS009 Disseminated Intravascular Coagulation 57 0.051
133
P CLL015 Collagen Disease 47 0.051
134
PRT030 Parathyroid Gland Disease 45 0.051
135
P EPL164 Epilepsy 71 0.050
136
c PNC108 Pancreatitis, Hereditary 70 0.050
137
CRB037 Cerebral Palsy 69 0.050
138
PSY004 Psychotic Disorder 67 0.050
139
ALC007 Alcohol Dependence 66 0.050
140
P PRS038 Personality Disorder 65 0.050
141
P DBT009 Diabetes Mellitus 64 0.050
142
P BND020 Bone Disease 59 0.050
143
P SLP005 Sleep Disorder 59 0.050
144
PRT058 Pure Autonomic Failure 59 0.050
145
ADN018 Adenoma 59 0.050
146
P ALC033 Alcohol Use Disorder 58 0.050
147
P INF032 Infertility 57 0.050
148
P PYL005 Pyelonephritis 56 0.050
149
P AGN002 Agnosia 55 0.050
150
CLL003 Cellulitis 54 0.050
151
PCT003 Pectus Excavatum 49 0.050
152
BNR002 Bone Resorption Disease 48 0.050
153
UMB002 Umbilical Hernia 46 0.050
154
P MYC033 Myoclonus 46 0.050
155
EPC002 Epicondylitis 41 0.050
156
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.050
157
PYR004 Pyuria 40 0.050
158
PRR001 Periarthritis 32 0.050
159
P CYS039 Cystic Kidney Disease 54 0.049
160
P LCT001 Lactic Acidosis 51 0.049
161
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.049
162
P HPT023 Hepatocellular Carcinoma 100 0.048
163
P LNG032 Lung Cancer 98 0.048
164
ESP021 Esophageal Cancer 90 0.048
165
MYL069 Myeloma, Multiple 85 0.048
166
P PRK057 Parkinson Disease, Late-Onset 78 0.048
167
P HRT032 Heart Disease 75 0.048
168
P SCH015 Schizophrenia 74 0.048
169
P NRB001 Neuroblastoma 72 0.048
170
CNG034 Congestive Heart Failure 69 0.048
171
BRN024 Bronchitis 68 0.048
172
CHC001 Chickenpox 60 0.048
173
PST028 Post-Traumatic Stress Disorder 58 0.048
174
PHR003 Pharyngitis 57 0.048
175
FRZ001 Frozen Shoulder 53 0.048
176
INT075 Intracranial Hypertension 53 0.048
177
c MCR113 Microvascular Complications of Diabetes 3 52 0.048
178
FDL002 Food Allergy 51 0.048
179
NRM004 Neuroma 51 0.048
180
NTR046 Neutrophil Migration 50 0.048
181
SBS004 Substance Dependence 48 0.048
182
ACT084 Acute Stress Disorder 47 0.048
183
P CLS010 Cluster Headache 42 0.048
184
c MCR130 Microvascular Complications of Diabetes 6 41 0.048
185
c MCR133 Microvascular Complications of Diabetes 4 41 0.048
186
c MCR112 Microvascular Complications of Diabetes 2 41 0.048
188
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.047
189
RCK004 Rickets 68 0.047
190
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.047
191
P CRD119 Cardiac Arrest 67 0.047
192
P ADL010 Adult Respiratory Distress Syndrome 65 0.047
193
MSC007 Muscle Hypertrophy 64 0.047
194
c PRC016 Pre-Eclampsia 63 0.047
195
TYP007 Typhoid Fever 63 0.047
196
P CRN300 Coronary Heart Disease 1 63 0.047
197
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.047
198
P ENC018 Encephalopathy 61 0.047
199
ACQ007 Acquired Immunodeficiency Syndrome 60 0.047
200
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.047
201
IGR001 Ige Responsiveness, Atopic 59 0.047
202
SPN027 Spinal Stenosis 59 0.047
203
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.047
204
ERY003 Erythema Multiforme 58 0.047
205
NWB001 Newborn Respiratory Distress Syndrome 58 0.047
206
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.047
207
URN010 Urinary Tract Obstruction 55 0.047
208
P INF037 Inflammatory Bowel Disease 54 0.047
209
P ART021 Arteriosclerosis 54 0.047
210
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.047
211
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.047
212
P RCT021 Rectum Cancer 52 0.047
213
PTH003 Pathologic Nystagmus 52 0.047
214
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.047
215
PLS009 Plasma Cell Neoplasm 51 0.047
216
TRM010 Traumatic Brain Injury 51 0.047
217
HRT011 Heart Septal Defect 50 0.047
218
BRS064 Bursitis 48 0.047
219
ASP007 Aspiration Pneumonia 48 0.047
220
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.047
221
SPC010 Speech and Communication Disorders 47 0.047
222
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.047
223
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.047
224
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.047
225
P BNG032 Benign Mesothelioma 46 0.047
226
P HRN001 Horner's Syndrome 45 0.047
227
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.047
228
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.047
229
CNN002 Cannabis Abuse 44 0.047
230
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.047
231
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.047
232
PLY068 Polysubstance Abuse 43 0.047
233
CNN001 Cannabis Dependence 40 0.047
234
HRW001 Hair Whorl 36 0.047
235
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.047
236
THR004 Thrombocytosis 51 0.046
237
CYS001 Cystic Fibrosis 81 0.045
238
ULC004 Ulcerative Colitis 73 0.045
239
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.045
240
SVR097 Severe Cutaneous Adverse Reaction 69 0.045
241
P LYM118 Lymphoma 68 0.045
242
P SKN015 Skin Carcinoma 66 0.045
243
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.045
244
PPL049 Papillon-Lefevre Syndrome 65 0.045
245
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.045
246
P HRP006 Herpes Simplex 65 0.045
247
ATH013 Atherosclerosis Susceptibility 65 0.045
248
PLM031 Poliomyelitis 64 0.045
249
P GLM045 Glioma 63 0.045
250
SKN016 Skin Disease 63 0.045
251
INT146 Intervertebral Disc Disease 63 0.045
252
LPD008 Lipid Metabolism Disorder 62 0.045
253
c SVR001 Severe Acute Respiratory Syndrome 62 0.045
254
RTN017 Retinal Detachment 61 0.045
255
SQM006 Squamous Cell Carcinoma 60 0.045
256
P ATR010 Atrial Heart Septal Defect 60 0.045
257
HYD002 Hydronephrosis 60 0.045
258
ETN001 Eating Disorder 60 0.045
259
GST045 Gastroenteritis 59 0.045
260
P INT070 Intestinal Obstruction 58 0.045
261
DSS008 Disease of Mental Health 58 0.045
262
GLS018 Glass Syndrome 57 0.045
263
GNR004 Generalized Anxiety Disorder 56 0.045
264
ALL010 Allergic Contact Dermatitis 56 0.045
265
AGN016 Aging 56 0.045
266
CLF004 Cleft Lip/palate 54 0.045
267
RFL001 Reflex Sympathetic Dystrophy 54 0.045
268
MMM001 Mammary Paget's Disease 53 0.045
269
DNT012 Dental Caries 53 0.045
270
ART140 Arteries, Anomalies of 52 0.045
271
AVD001 Avoidant Personality Disorder 51 0.045
272
SPN019 Spondylolisthesis 51 0.045
273
DYS073 Dysphagia 50 0.045
274
P MGR001 Migraine Without Aura 49 0.045
275
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.045
276
VCC001 Vaccinia 49 0.045
277
GLL048 Glial Tumor 45 0.045
278
ASP008 Aspiration Pneumonitis 45 0.045
279
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.045
280
SPN369 Spinal Disease 43 0.045
281
MCR011 Microinvasive Gastric Cancer 43 0.045
282
TRP009 Triple X Syndrome 42 0.045
283
DRG024 Drug Allergy 42 0.045
284
49X006 49, Xxxxy Syndrome 41 0.045
285
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 40 0.045
286
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.045
287
ALG001 Algoneurodystrophy 39 0.045
288
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.045
289
ABD010 Abdominal Wall Defect 36 0.045
290
c PRS136 Prostate Cancer, Hereditary, 6 33 0.045
291
c PRS130 Prostate Cancer, Hereditary, 8 32 0.045
292
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.045
293
ERY066 Erythema Multiforme Major 30 0.045
294
PRC051 Paracetamol Poisoning 30 0.045
295
TMP019 Temporomandibular Joint Anomaly 28 0.045
296
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.043
297
END057 Endometrial Cancer 74 0.043
298
c MNN043 Meningioma, Familial 74 0.043
299
CRH001 Crohn's Disease 74 0.043
300
c EXD008 Exudative Vitreoretinopathy 1 71 0.043
301
PRP027 Peripheral Vascular Disease 71 0.043
302
MYL009 Myelodysplastic Syndrome 70 0.043
303
P TTR001 Tetralogy of Fallot 70 0.043
304
P MYP004 Myopathy 70 0.043
305
P LPR021 Leprosy 3 69 0.043
306
ART016 Aortic Aneurysm 69 0.043
307
P LKM002 Leukemia 68 0.043
308
P INF038 Influenza 68 0.043
309
P THR014 Thrombocytopenia 67 0.043
310
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.043
311
TTN003 Tetanus 65 0.043
312
P DYS154 Dystonia 65 0.043
313
TBC004 Tobacco Addiction 64 0.043
314
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.043
315
P NTR004 Neutropenia 63 0.043
316
P HYP069 Hyperparathyroidism 63 0.043
317
HMT002 Hematologic Cancer 62 0.043
318
P ESP024 Esophagitis 62 0.043
319
TXC005 Toxic Shock Syndrome 62 0.043
320
HYP066 Hyperglycemia 61 0.043
321
c SCL052 Scleroderma, Familial Progressive 61 0.043
322
P VNT002 Ventricular Septal Defect 60 0.043
323
HPT019 Hepatic Encephalopathy 60 0.043
324
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.043
325
THY029 Thyroid Carcinoma 59 0.043
326
HLC007 Helicobacter Pylori Infection 59 0.043
327
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.043
328
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.043
329
P MMP001 Mumps 58 0.043
330
THY122 Thyroid Gland Cancer 57 0.043
331
c MST023 Mesothelioma, Malignant 57 0.043
332
STR081 Stormorken Syndrome 57 0.043
333
AYM001 Ayme-Gripp Syndrome 57 0.043
334
P BPL003 Bipolar Disorder 56 0.043
335
ATR057 Atrioventricular Block 55 0.043
336
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.043
337
P MYP006 Myopia 55 0.043
338
P PTT006 Pituitary Adenoma 55 0.043
339
CRT017 Cartilage Disease 54 0.043
340
P LTR001 Lateral Sclerosis 54 0.043
341
MST005 Mastitis 53 0.043
342
MTN003 Motion Sickness 53 0.043
343
c XNT010 Xanthinuria, Type I 53 0.043
344
SPN035 Spindle Cell Sarcoma 53 0.043
345
TXC002 Toxic Encephalopathy 53 0.043
346
EXP004 Exophthalmos 52 0.043
347
PRP016 Paraplegia 52 0.043
348
THR016 Thrombophlebitis 51 0.043
349
P ECL001 Eclampsia 50 0.043
350
BRN071 Brain Injury 49 0.043
351
URM002 Uremia 49 0.043
352
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.043
353
DGN001 Degenerative Disc Disease 48 0.043
354
BNN003 Bone Inflammation Disease 48 0.043
355
P TRT019 Torticollis 48 0.043
356
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.043
357
LYM019 Lymphosarcoma 46 0.043
358
ANL022 Anal Fistula 46 0.043
359
c CHR048 Chronic Rhinitis 46 0.043
360
EXS001 Exostosis 46 0.043
361
HYD005 Hydrocele 46 0.043
362
HPT004 Hepatic Coma 45 0.043
363
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.043
364
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.043
365
DVR002 Diverticulitis 43 0.043
366
c MJR024 Major Affective Disorder 9 41 0.043
367
RDN001 Reading Disorder 40 0.043
368
FML039 Female Reproductive System Disease 39 0.043
369
ALX002 Alexithymia 38 0.043
370
c MJR022 Major Affective Disorder 8 38 0.043
371
HNS001 Hansen's Disease 34 0.043
372
PRS064 Persistent Vegetative State 33 0.043
373
FNT004 Fainting 30 0.043
374
SPN392 Spondylosis, Cervical 30 0.043
375
RSP007 Respiratory Distress Syndrome, Infant 30 0.043
376
PRS120 Persistent Idiopathic Facial Pain 28 0.043
377
c CNG129 Congenital Torticollis 23 0.043
378
NRL016 Neural Tube Defects 82 0.041
379
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.041
380
CNN003 Conn's Syndrome 79 0.041
381
IMM167 Immune Deficiency Disease 78 0.041
382
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.041
383
c ATR087 Atrial Standstill 1 75 0.041
384
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.041
385
P ATS364 Autism 70 0.041
386
P AMY004 Amyloidosis 70 0.041
387
LYM133 Lymphoma, Hodgkin, Classic 69 0.041
388
c INF071 Inflammatory Bowel Disease 1 67 0.041
389
P FLL037 Follicular Lymphoma 67 0.041
390
P HYP098 Hypereosinophilic Syndrome 67 0.041
391
P MLG056 Malignant Hyperthermia 67 0.041
392
PRT010 Parathyroid Carcinoma 67 0.041
393
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.041
394
P MNN013 Meningitis 66 0.041
395
P DRM053 Dermatitis, Atopic 66 0.041
396
LNG039 Lung Squamous Cell Carcinoma 66 0.041
397
PND002 Pendred Syndrome 65 0.041
398
c DBT099 Diabetes Mellitus, Type I 65 0.041
399
CLN015 Colon Adenocarcinoma 65 0.041
400
P THY023 Thymoma 65 0.041
401
NRM005 Neuromuscular Disease 64 0.041
402
c JVN010 Juvenile Rheumatoid Arthritis 64 0.041
403
P HYP055 Hypoplastic Left Heart Syndrome 63 0.041
404
CHN016 Cohen Syndrome 63 0.041
405
HYP780 Hypoadrenocorticism, Familial 63 0.041
406
CLT003 Colitis 62 0.041
407
P PLY014 Polycystic Kidney Disease 62 0.041
408
P HYP750 Hypertriglyceridemia, Familial 62 0.041
409
MNN042 Meningioma, Radiation-Induced 62 0.041
410
P PRP029 Porphyria 62 0.041
411
OST003 Osteonecrosis 61 0.041
412
DCB001 Decubitus Ulcer 61 0.041
413
DPH001 Diphtheria 60 0.041
414
c LPM012 Lipomatosis, Multiple 60 0.041
415
CRD223 Cardiac Arrhythmia 60 0.041
416
VRC005 Varicose Veins 60 0.041
417
ORL011 Oral Cancer 60 0.041
418
P MYC008 Myocarditis 59 0.041
419
GNG013 Gingivitis 59 0.041
420
GLB001 Gilbert Syndrome 58 0.041
421
P BCL017 B-Cell Lymphoma 58 0.041
422
BRS051 Breast Disease 58 0.041
423
P MTR012 Mitral Valve Disease 58 0.041
424
P END033 Endocarditis 57 0.041
425
P MYS005 Myositis 56 0.041
426
P FBR017 Fibrosarcoma 56 0.041
427
PRS047 Prostatitis 56 0.041
428
NRL004 Neuroleptic Malignant Syndrome 56 0.041
429
MTH009 Mouth Disease 56 0.041
430
GST050 Gastrointestinal System Disease 56 0.041
431
P ATR001 Atrioventricular Septal Defect 55 0.041
432
PLV003 Pelvic Inflammatory Disease 55 0.041
433
P DYS193 Dystonia 11, Myoclonic 55 0.041
434
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.041
435
END040 Endogenous Depression 55 0.041
436
TRD006 Tardive Dyskinesia 54 0.041
437
GLC003 Glucose Intolerance 54 0.041
438
P RST001 Restless Legs Syndrome 54 0.041
439
AMN001 Amenorrhea 54 0.041
440
PTT009 Pituitary Gland Disease 54 0.041
441
P INS002 in Situ Carcinoma 53 0.041
442
HRT012 Heart Valve Disease 53 0.041
443
c PRD040 Periodontitis, Chronic 53 0.041
444
INF034 Infective Endocarditis 53 0.041
445
GTR002 Goiter 53 0.041
446
GSG001 Gas Gangrene 53 0.041
447
NRT001 Neurotic Disorder 53 0.041
448
P PNC025 Panic Disorder 53 0.041
449
P RTN018 Retinal Disease 53 0.041
450
c VRL010 Viral Hepatitis 52 0.041
451
ACR041 Acromelic Frontonasal Dysostosis 52 0.041
452
NRT004 Neuritis 52 0.041
453
c THY107 Thymoma, Familial 52 0.041
454
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.041
455
P MGR003 Migraine with Aura 52 0.041
456
LMY002 Leiomyoma 52 0.041
457
SPS003 Spastic Diplegia 51 0.041
458
c PNC106 Pancreatic Agenesis 1 51 0.041
459
P AST007 Astrocytoma 51 0.041
460
BHR001 Behr Syndrome 51 0.041
461
SPN021 Spinal Meningioma 50 0.041
462
c SVR005 Severe Pre-Eclampsia 50 0.041
463
FSC004 Fasciitis 50 0.041
464
c INF145 Infantile Liver Failure Syndrome 1 50 0.041
465
PLC008 Placenta Disease 50 0.041
466
BNG036 Bone Giant Cell Tumor 49 0.041
467
CCN002 Cocaine Abuse 49 0.041
468
c FLL041 Follicular Lymphoma 1 49 0.041
469
P BRS053 Breast Fibroadenoma 49 0.041
470
PNC034 Pancreas Disease 48 0.041
471
LPT006 Leptin Receptor Deficiency 48 0.041
472
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.041
473
CRD001 Cardiac Tamponade 47 0.041
474
P OVR046 Ovarian Cyst 47 0.041
475
RYN005 Raynaud Phenomenon 47 0.041
476
ATN005 Autonomic Dysfunction 46 0.041
477
SPN020 Spondylosis 46 0.041
478
KRT013 Keratolytic Winter Erythema 46 0.041
479
P MTH007 Methemoglobinemia 46 0.041
480
c MLG068 Malignant Glioma 46 0.041
481
ACT003 Acute Kidney Tubular Necrosis 45 0.041
482
CNT017 Central Nervous System Origin Vertigo 45 0.041
483
MYF001 Myofibroma 45 0.041
484
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 0.041
485
PTT037 Pituitary Tumors 44 0.041
486
P BLP003 Blepharospasm 44 0.041
487
PPL001 Papillary Adenoma 44 0.041
488
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.041
489
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 43 0.041
490
LWC001 Low Compliance Bladder 43 0.041
491
ORL015 Oral Squamous Cell Carcinoma 43 0.041
492
P HYP265 Hypotonia 43 0.041
493
P MJR007 Major Affective Disorder 1 43 0.041
494
RST023 Resting Heart Rate, Variation in 41 0.041
495
SCR001 Secretory Meningioma 41 0.041
496
CRB086 Cerebral Aneurysms 40 0.041
497
P OTT001 Otitis Externa 39 0.041
498
c CHR682 Chronic Bilirubin Encephalopathy 39 0.041
499
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.041
500
BLR004 Biliary Dyskinesia 38 0.041
501
WHP002 Whiplash 36 0.041
502
PPT002 Peptic Ulcer Perforation 36 0.041
503
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.041
504
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.041
505
SPP003 Suppurative Periapical Periodontitis 34 0.041
506
PLN007 Plantar Fasciitis 32 0.041
507
SNG003 Single Ventricular Heart 30 0.041
508
PST092 Posttransplant Acute Limbic Encephalitis 29 0.041
509
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.039
510
MLR004 Malaria 81 0.039
511
P GLM040 Glioma Susceptibility 1 81 0.039
512
P MDL005 Medulloblastoma 77 0.039
513
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.039
514
KPS004 Kaposi Sarcoma 75 0.039
515
BRN028 Brain Cancer 74 0.039
516
SVR004 Severe Combined Immunodeficiency 73 0.039
517
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.039
518
c HPT073 Hepatitis C Virus 72 0.039
519
P GRF003 Graft-Versus-Host Disease 72 0.039
520
c LKM063 Leukemia, Chronic Myeloid 72 0.039
521
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.039
522
P BRG001 Brugada Syndrome 71 0.039
523
P SRC025 Sarcoidosis 1 70 0.039
524
GST040 Gastric Adenocarcinoma 70 0.039
525
MYL005 Myelofibrosis 70 0.039
526
P FRG001 Fragile X Syndrome 70 0.039
527
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.039
528
PLY001 Polycythemia Vera 69 0.039
529
P MLN008 Melanoma 69 0.039
530
EWN003 Ewing Sarcoma 69 0.039
531
MST024 Mastocytosis, Cutaneous 69 0.039
532
P TMP003 Temporal Arteritis 68 0.039
533
P MYC084 Mycobacterium Tuberculosis 1 68 0.039
534
CHL065 Cholangiocarcinoma 68 0.039
535
CMM004 Common Variable Immunodeficiency 68 0.039
536
OBS002 Obsessive-Compulsive Disorder 68 0.039
537
SKN019 Skin Melanoma 68 0.039
538
P ESS003 Essential Thrombocythemia 68 0.039
539
PNC129 Pancreatic Adenocarcinoma 68 0.039
540
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.039
541
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.039
542
FCT007 Factor Vii Deficiency 67 0.039
543
P OLG002 Oligodendroglioma 67 0.039
544
BRK010 Burkitt Lymphoma 67 0.039
545
c HMP029 Hemophilia a 67 0.039
546
P BLD062 Bile Duct Cancer 67 0.039
547
P CLC063 Celiac Disease 1 66 0.039
548
P LNG028 Long Qt Syndrome 66 0.039
549
GLL008 Gilles De La Tourette Syndrome 66 0.039
550
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.039
551
P HYD006 Hydrocephalus 66 0.039
552
MYL031 Myeloproliferative Neoplasm 66 0.039
553
DMN031 Dementia, Lewy Body 65 0.039
554
KRT019 Keratitis, Hereditary 65 0.039
555
P MTR014 Motor Neuron Disease 65 0.039
556
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.039
557
c ART101 Aortic Valve Disease 2 65 0.039
558
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.039
559
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.039
560
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.039
561
NRF007 Neurofibroma 64 0.039
562
OVR029 Ovarian Hyperstimulation Syndrome 64 0.039
563
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.039
564
DGR001 Digeorge Syndrome 64 0.039
565
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.039
566
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.039
567
DSM004 Desmoid Tumor 64 0.039
568
KND001 Kindler Syndrome 64 0.039
569
OST017 Osteomyelitis 64 0.039
570
c DPH024 Diaphragmatic Hernia, Congenital 63 0.039
571
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.039
572
P ANR048 Aniridia 1 63 0.039
573
PLG002 Plague 63 0.039
574
P MVM001 Movement Disease 63 0.039
575
P LMY004 Leiomyosarcoma 63 0.039
576
ANR007 Anorexia Nervosa 63 0.039
577
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.039
578
c HPT001 Hepatitis C 62 0.039
579
c HPT003 Hepatitis a 62 0.039
580
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.039
581
P TRC086 Trichohepatoenteric Syndrome 1 62 0.039
582
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 0.039
583
BRS099 Breast Ductal Carcinoma 62 0.039
584
NTR005 Nutritional Deficiency Disease 62 0.039
585
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.039
586
FTT001 Fatty Liver Disease 61 0.039
587
INT002 Intermittent Claudication 61 0.039
588
c WLM018 Wilms Tumor 5 61 0.039
589
VRL011 Viral Infectious Disease 61 0.039
590
P HMN010 Hemangioma 61 0.039
591
NRL005 Neurilemmoma 60 0.039
592
P MYL006 Myeloid Leukemia 60 0.039
593
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.039
594
P TST021 Testicular Germ Cell Tumor 60 0.039
595
P BNG030 Benign Ependymoma 60 0.039
596
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.039
597
STT001 Status Epilepticus 60 0.039
598
P CHR285 Chronic Myelomonocytic Leukemia 60 0.039
599
P OPT006 Optic Nerve Disease 60 0.039
600
SPP011 Suppression of Tumorigenicity 12 59 0.039
601
PRT013 Portal Hypertension 59 0.039
602
c HPT016 Hepatitis B 59 0.039
603
c PCH015 Pachyonychia Congenita 1 59 0.039
604
CHL123 Chlamydia 59 0.039
605
P LYM033 Lymphoproliferative Syndrome 59 0.039
606
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.039
607
P MLN069 Melanoma, Uveal 59 0.039
608
DCT002 Ductal Carcinoma in Situ 59 0.039
609
P BRS044 Breast Adenocarcinoma 59 0.039
610
GRD007 Grade Iii Astrocytoma 59 0.039
611
P HMN036 Hemangiopericytoma, Malignant 59 0.039
612
BRN002 Bronchiolitis 59 0.039
613
VLV032 Vulva Cancer 59 0.039
614
c ACT073 Acute Leukemia 58 0.039
615
P SYP003 Syphilis 58 0.039
616
TTZ003 Tietz Albinism-Deafness Syndrome 58 0.039
617
THY025 Thymus Cancer 58 0.039
618
P CND004 Candidiasis 58 0.039
619
P GLL018 Gallbladder Cancer 57 0.039
620
P PLV020 Pelvic Organ Prolapse 57 0.039
621
IRN002 Iron Metabolism Disease 57 0.039
622
BRN056 Bronchopulmonary Dysplasia 57 0.039
623
MNR012 Meniere Disease 57 0.039
624
P PLY041 Polymyositis 57 0.039
625
P SLV026 Salivary Gland Carcinoma 57 0.039
626
BRD001 Brody Myopathy 57 0.039
627
P FCL005 Focal Segmental Glomerulosclerosis 57 0.039
628
THY022 Thymic Carcinoma 57 0.039
629
BLR008 Bilirubin Metabolic Disorder 57 0.039
630
VSC002 Vascular Dementia 57 0.039
631
P URF003 Urofacial Syndrome 1 57 0.039
632
SCH014 Schistosomiasis 57 0.039
633
INT303 Intracranial Hypertension, Idiopathic 57 0.039
634
P PLY018 Polycythemia 56 0.039
635
P PLY011 Polycystic Ovary Syndrome 56 0.039
636
PLS011 Plasmacytoma 56 0.039
637
ADN027 Adenomyosis 56 0.039
638
c ESS001 Essential Tremor 56 0.039
639
P MTC069 Mitochondrial Disorders 56 0.039
640
SFT003 Soft Tissue Sarcoma 56 0.039
641
SCH003 Schizophreniform Disorder 56 0.039
642
ISL001 Islet Cell Tumor 56 0.039
643
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.039
644
ACS001 Acoustic Neuroma 56 0.039
645
P NRF002 Neurofibromatosis 56 0.039
646
ORL005 Oral Candidiasis 56 0.039
647
BRN012 Bronchiolitis Obliterans 55 0.039
648
c FML035 Familial Hyperlipidemia 55 0.039
649
ORP003 Oropharynx Cancer 55 0.039
650
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.039
651
LMB062 Limb Ischemia 55 0.039
652
P MLN007 Male Infertility 55 0.039
653
c BCT007 Bacterial Meningitis 55 0.039
654
DFF005 Diffuse Large B-Cell Lymphoma 55 0.039
655
ANG005 Anogenital Venereal Wart 55 0.039
656
OCL009 Ocular Cancer 55 0.039
657
P VNS003 Venous Insufficiency 55 0.039
658
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.039
659
INT007 Intermediate Coronary Syndrome 55 0.039
660
P SPN052 Spondyloarthropathy 54 0.039
661
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.039
662
GLS001 Gliosarcoma 54 0.039
663
FCL014 Focal Epilepsy 54 0.039
664
VLC001 Velocardiofacial Syndrome 54 0.039
665
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.039
666
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.039
667
CLL010 Cellular Ependymoma 54 0.039
668
PLM010 Pulmonary Edema 54 0.039
669
LYM040 Lymphoblastic Lymphoma 54 0.039
670
NNL006 Non-Alcoholic Steatohepatitis 54 0.039
671
CLR030 Clear Cell Renal Cell Carcinoma 53 0.039
672
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.039
673
P TCD001 Tic Disorder 53 0.039
674
PST046 Post-Transplant Lymphoproliferative Disease 53 0.039
675
CRH005 Crohn's Colitis 53 0.039
676
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.039
677
BRD004 Borderline Personality Disorder 53 0.039
678
P HMR003 Hemorrhagic Disease 53 0.039
679
P FBR031 Febrile Seizures 53 0.039
680
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.039
681
PRP080 Peripheral Artery Disease 53 0.039
682
P INT068 Intestinal Disease 53 0.039
683
c CNT035 Central Nervous System Disease 52 0.039
684
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.039
685
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.039
686
c CRS016 Crisponi/cold-Induced Sweating Syndrome 1 52 0.039
687
IMP005 Impotence 52 0.039
688
P MSC003 Muscular Atrophy 52 0.039
689
BWN001 Bowen-Conradi Syndrome 52 0.039
690
P OVR049 Ovarian Disease 52 0.039
691
P BRN035 Brain Stem Glioma 52 0.039
692
PRV004 Periventricular Leukomalacia 52 0.039
693
P SPP010 Suppressor of Tumorigenicity 3 51 0.039
694
FCT001 Factor Viii Deficiency 51 0.039
695
KRT009 Keratosis 51 0.039
696
INT079 Intrahepatic Cholangiocarcinoma 51 0.039
697
ESP002 Esophageal Varix 51 0.039
698
P PRC012 Pericardial Effusion 51 0.039
699
TNG007 Tongue Carcinoma 51 0.039
700
SKN013 Skin Benign Neoplasm 51 0.039
701
PNM005 Pneumonic Plague 51 0.039
702
ACT017 Acute Chest Syndrome 51 0.039
703
INT071 Intestinal Perforation 51 0.039
704
CHR005 Chorioamnionitis 51 0.039
705
c ALM001 Al Amyloidosis 50 0.039
706
GNT002 Giant Cell Glioblastoma 50 0.039
707
SCH012 Schizoaffective Disorder 50 0.039
708
c PRM012 Primary Polycythemia 50 0.039
709
P OVR082 Overgrowth Syndrome 50 0.039
710
BRX001 Bruxism 50 0.039
711
RTN003 Retinal Ischemia 50 0.039
712
RSP006 Respiratory System Disease 50 0.039
713
PRT018 Portal Vein Thrombosis 50 0.039
714
P KRT007 Keratoconus 50 0.039
715
P OBS001 Obstructive Jaundice 50 0.039
716
P PNB001 Pineoblastoma 50 0.039
717
c DYS119 Dystonia 9 50 0.039
718
ATY042 Atypical Chronic Myeloid Leukemia 49 0.039
719
c CHR418 Chronic Leukemia 49 0.039
720
c THR090 Thrombocythemia 1 49 0.039
721
PPL021 Papilledema 49 0.039
722
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.039
723
AMB002 Amblyopia 49 0.039
724
P MST002 Mast-Cell Leukemia 49 0.039
725
BKR002 Baker-Gordon Syndrome 49 0.039
726
MTC005 Mitochondrial Metabolism Disease 49 0.039
727
ACT029 Acute Interstitial Pneumonia 49 0.039
728
PTH002 Pathological Gambling 49 0.039
729
SBP001 Subependymal Giant Cell Astrocytoma 49 0.039
730
QDR001 Quadriplegia 48 0.039
731
RYN001 Raynaud Disease 48 0.039
732
c BCT013 Bacterial Pneumonia 48 0.039
733
c DSB006 Desbuquois Dysplasia 1 48 0.039
734
CCN001 Cocaine Dependence 48 0.039
735
RFR010 Refractory Anemia 48 0.039
736
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.039
737
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.039
738
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.039
739
HMP001 Hemopericardium 48 0.039
740
URN009 Urinary System Disease 48 0.039
741
c MTR002 Mitral Valve Insufficiency 48 0.039
742
DSM003 Desmoid Disease, Hereditary 48 0.039
743
HYP025 Hyperphosphatemia 48 0.039
744
P DPY001 Dupuytren Contracture 48 0.039
745
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.039
746
THY128 Thyroid Tumor 47 0.039
747
P ERY008 Erythromelalgia 47 0.039
748
AST006 Astigmatism 47 0.039
749
KRT002 Keratomalacia 47 0.039
750
RTC005 Reticulosarcoma 47 0.039
751
c CNG216 Congenital Hydrocephalus 47 0.039
752
PLS025 Plasmablastic Lymphoma 47 0.039
753
ANV001 Anovulation 47 0.039
754
CNT033 Central Nervous System Cancer 47 0.039
755
P RTN014 Retinal Artery Occlusion 47 0.039
756
NSS002 Neisseria Meningitidis Infection 47 0.039
757
P BLD051 Blood Coagulation Disease 46 0.039
758
TST014 Testicular Cancer 46 0.039
759
BCK003 Background Diabetic Retinopathy 46 0.039
760
PRP017 Periapical Periodontitis 46 0.039
761
TTH006 Tooth Disease 46 0.039
762
SMT001 Somatization Disorder 46 0.039
763
MYC005 Myocardial Stunning 46 0.039
764
MNN020 Meningococcal Infection 46 0.039
765
CLN045 Colonic Benign Neoplasm 46 0.039
766
MGC001 Megacolon 46 0.039
767
ANP006 Anaplastic Ependymoma 46 0.039
768
RCT017 Rectal Disease 46 0.039
769
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.039
770
SYN036 Syncope 45 0.039
771
RTR008 Root Resorption 45 0.039
772
MXD026 Mixed Glioma 45 0.039
773
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.039
774
URT010 Ureteral Obstruction 45 0.039
775
INT253 Intestinal Benign Neoplasm 45 0.039
776
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.039
777
CRB004 Cerebral Artery Occlusion 45 0.039
778
IMM136 Immune System Disease 45 0.039
779
CRT015 Carotid Artery Occlusion 45 0.039
780
ATN004 Autonomic Neuropathy 45 0.039
781
OVR112 Ovarian Germ Cell Cancer 45 0.039
782
ANS012 Anus Disease 45 0.039
783
c DRM054 Dermatitis, Atopic, 2 44 0.039
784
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.039
785
IRT001 Iritis 44 0.039
786
GNG003 Gingival Recession 44 0.039
787
TNS014 Tenosynovitis 44 0.039
788
PRT035 Peritoneum Cancer 44 0.039
789
SPN040 Spinal Cancer 44 0.039
790
P BCT020 Bacteremia 2 44 0.039
791
P EPN001 Ependymoblastoma 44 0.039
792
P BNG095 Benign Giant Cell Tumor 44 0.039
793
DMP001 Dumping Syndrome 44 0.039
794
EMP001 Empty Sella Syndrome 44 0.039
795
CVD001 Covid-19 44 0.039
796
CRB090 Cerebral Hypoxia 44 0.039
797
ANP009 Anaplastic Oligodendroglioma 43 0.039
798
P BLD036 Bile Duct Disease 43 0.039
799
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.039
800
SKN005 Skin Atrophy 43 0.039
801
RFR003 Refractive Error 43 0.039
802
URT037 Urethral Stricture 43 0.039
803
c SRC023 Sarcoidosis 2 43 0.039
804
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.039
805
HMP009 Haemophilus Influenzae 43 0.039
806
STL007 Steel Syndrome 43 0.039
807
BNS003 Binswanger's Disease 42 0.039
808
ORB013 Orbital Disease 42 0.039
809
LMR001 Lemierre's Syndrome 42 0.039
810
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.039
811
c MLG064 Malignant Ependymoma 41 0.039
812
MDS018 Mediastinal Cancer 41 0.039
813
CRN322 Coronavirus Infectious Disease 40 0.039
814
P MLG074 Malignant Mesenchymoma 40 0.039
815
BRN026 Branch Retinal Artery Occlusion 40 0.039
816
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.039
817
NRV004 Nerve Compression Syndrome 40 0.039
818
ANG049 Angioedema Induced by Ace Inhibitors 40 0.039
819
PRM020 Premenstrual Tension 40 0.039
820
C1N001 C1 Inhibitor Deficiency 39 0.039
821
PLC009 Placenta Praevia 39 0.039
822
SPP007 Suppression Amblyopia 39 0.039
823
SPR024 Supratentorial Cancer 39 0.039
824
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.039
825
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.039
826
ANT019 Anterograde Amnesia 38 0.039
827
c PLY105 Polycystic Ovary Syndrome 1 38 0.039
828
CVT001 Cavitary Optic Disc Anomalies 38 0.039
829
c OVR114 Ovarian Cancer 1 38 0.039
830
OPT010 Optic Papillitis 38 0.039
831
ALG027 Al-Gazali-Bakalinova Syndrome 38 0.039
832
CDQ001 Cauda Equina Syndrome 38 0.039
833
TXC001 Toxic Megacolon 38 0.039
834
DDN027 Duodenum Disease 37 0.039
835
c LPR022 Leprosy 2 37 0.039
836
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.039
837
P DNT007 Dentin Sensitivity 36 0.039
838
PRR013 Prurigo Nodularis 36 0.039
839
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.039
840
CRB079 Cerebrospinal Fluid Leak 35 0.039
841
ANS004 Anisometropia 35 0.039
842
LCL004 Localized Osteosarcoma 35 0.039
843
NRD001 Neurodermatitis 35 0.039
844
c MJR008 Major Affective Disorder 2 35 0.039
845
DDN009 Duodenal Obstruction 34 0.039
846
CRV025 Cervical Incompetence 34 0.039
847
GRM010 Germ Cells Tumors 34 0.039
848
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.039
849
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.039
850
c ADL008 Adult Oligodendroglioma 34 0.039
851
PLM028 Pulmonary Coin Lesion 33 0.039
852
c MJR023 Major Affective Disorder 7 33 0.039
853
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 33 0.039
854
c MJR003 Major Affective Disorder 6 33 0.039
855
c MJR006 Major Affective Disorder 5 33 0.039
856
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.039
857
SHL001 Shoulder Impingement Syndrome 32 0.039
858
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.039
860
CLF044 Cleft Palate, Cardiac Defect, Genital Anomalies, and Ectrodactyly 31 0.039
861
c ADL054 Adult Brain Stem Glioma 30 0.039
862
CRD220 Cardiac Valvular Defect, Developmental 29 0.039
863
c MJR004 Major Affective Disorder 4 28 0.039
864
DQR001 De Quervain Disease 28 0.039
865
P CNT036 Central Nervous System Germ Cell Tumor 28 0.039
866
PRC001 Pericoronitis 28 0.039
867
CGN007 Cognitive Function 1, Social 27 0.039
868
DMN026 Dementia Pugilistica 27 0.039
869
CYT018 Cytochrome P450 2d6 Variant 27 0.039
870
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.039
871
PGM030 Pigmentation Anomaly of the Skin 26 0.039
872
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.039
873
MLG164 Malignant Epithelial Tumor of Ovary 26 0.039
874
FTL073 Fetal Anticonvulsant Syndrome 26 0.039
875
c ATS371 Autism 6 25 0.039
876
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.039
877
DVR001 Diverticulitis of Colon 25 0.039
878
HRP008 Herpes Simiae 25 0.039
879
INT053 Intracranial Vasospasm 24 0.039
880
MNN006 Meninges Hemangiopericytoma 23 0.039
881
ADS015 Aids Wasting Syndrome 22 0.039
882
HML018 Homologous Wasting Disease 22 0.039
884
HYP705 Hyperadrenalism 20 0.039
885
HPS001 Hip Subluxation 20 0.039
886
c MLG023 Malignant Adult Ependymoma 15 0.039
887
P INT320 Intelligence Quantitative Trait Locus 1 15 0.039
888
c ADL045 Adult Ependymoblastoma 14 0.039
889
PNL001 Pineal Gland Astrocytoma 14 0.039
890
MTS005 Metastatic Squamous Neck Cancer with Occult Primary 11 0.039
892
P ATX030 Ataxia-Telangiectasia 82 0.036
893
c FNC027 Fanconi Anemia, Complementation Group a 81 0.036
894
c DLT002 Dilated Cardiomyopathy 79 0.036
895
P LKM071 Leukemia, Chronic Lymphocytic 79 0.036
896
INS024 Insulin-Like Growth Factor I 79 0.036
897
P LNG064 Lung Cancer Susceptibility 3 78 0.036
898
P LYN001 Lynch Syndrome 77 0.036
899
c TBR025 Tuberous Sclerosis 1 77 0.036
900
c NRF024 Neurofibromatosis, Type I 77 0.036
901
PHN003 Phenylketonuria 75 0.036
902
c ART115 Aortic Valve Disease 1 75 0.036
903
ADR007 Adrenoleukodystrophy 75 0.036
904
c BTT014 Beta-Thalassemia 74 0.036
905
c HYP836 Hypercholesterolemia, Familial, 1 73 0.036
906
BSL036 Basal Cell Nevus Syndrome 73 0.036
907
MSC157 Muscular Dystrophy, Duchenne Type 72 0.036
908
SCH036 Scheie Syndrome 72 0.036
909
c TBR026 Tuberous Sclerosis 2 72 0.036
910
P JBR020 Joubert Syndrome 1 72 0.036
911
P HNT016 Huntington Disease 72 0.036
912
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.036
913
P WSK001 Wiskott-Aldrich Syndrome 72 0.036
914
P PHC003 Pheochromocytoma 71 0.036
915
BHC003 Behcet Syndrome 71 0.036
916
MLT157 Multiple System Atrophy 1 70 0.036
917
c GLY008 Glycogen Storage Disease Ii 70 0.036
918
P HYP061 Hypertrophic Cardiomyopathy 70 0.036
919
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.036
920
SMT004 Smith-Lemli-Opitz Syndrome 70 0.036
921
P TBR001 Tuberous Sclerosis 70 0.036
922
P DMN001 Diamond-Blackfan Anemia 69 0.036
923
P ASP006 Aspergillosis 69 0.036
924
P HYP086 Hypothyroidism 69 0.036
925
LYM007 Lymphangioleiomyomatosis 69 0.036
926
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.036
927
NVS017 Nevus, Epidermal 68 0.036
928
P SYS005 Systemic Scleroderma 68 0.036
929
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.036
930
HYL004 Hyaline Fibromatosis Syndrome 67 0.036
931
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.036
932
c HYP768 Hyperlipoproteinemia, Type I 67 0.036
933
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.036
934
P CHR012 Chronic Granulomatous Disease 67 0.036
935
P PRP003 Porphyria Cutanea Tarda 67 0.036
936
c ATS007 Autism Spectrum Disorder 67 0.036
937
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.036
938
P MSC005 Muscular Dystrophy 66 0.036
939
MYX005 Myxoid Liposarcoma 66 0.036
940
ACH004 Achondroplasia 66 0.036
941
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.036
943
c HRD010 Hereditary Spastic Paraplegia 66 0.036
944
CHG001 Chagas Disease 66 0.036
945
CNC002 Cinca Syndrome 65 0.036
946
ACR006 Aceruloplasminemia 65 0.036
947
P LPS002 Liposarcoma 65 0.036
948
P MTR004 Maturity-Onset Diabetes of the Young 65 0.036
949
PRP001 Propionic Acidemia 65 0.036
950
BRR014 Barrett Esophagus 65 0.036
951
GRN037 Granulomatosis with Polyangiitis 65 0.036
952
MRK001 Merkel Cell Carcinoma 65 0.036
953
c WLM013 Wilms Tumor 1 65 0.036
954
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.036
955
KWS002 Kawasaki Disease 65 0.036
956
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 65 0.036
957
MCK007 Muckle-Wells Syndrome 65 0.036
958
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.036
959
LYS012 Lysosomal Acid Lipase Deficiency 65 0.036
960
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.036
961
ANG020 Angiosarcoma 64 0.036
962
P MST009 Mastocytosis 64 0.036
963
CLR108 Colorectal Adenoma 64 0.036
964
P FRD001 Friedreich Ataxia 64 0.036
965
LYM017 Lyme Disease 64 0.036
966
MGK001 Megakaryocytic Leukemia 64 0.036
967
P RHB003 Rhabdomyosarcoma 63 0.036
968
KRN002 Kearns-Sayre Syndrome 63 0.036
969
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.036
970
CYS013 Cystinuria 63 0.036
971
c MLG084 Malignant Fibrous Histiocytoma 63 0.036
972
END041 Endometrial Adenocarcinoma 63 0.036
973
c SYS004 Systemic Mastocytosis 63 0.036
974
TRN015 Transient Cerebral Ischemia 63 0.036
975
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.036
976
c ATM011 Autoimmune Hepatitis 63 0.036
977
c GLC092 Glaucoma, Primary Open Angle 62 0.036
978
c ALP101 Alpha-Thalassemia 62 0.036
979
c LCL006 Localized Scleroderma 62 0.036
980
TKY002 Takayasu Arteritis 62 0.036
981
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.036
982
P SPN046 Spinal Muscular Atrophy 62 0.036
983
PRM126 Primary Peritoneal Carcinoma 62 0.036
984
c DYS056 Dystonia 12 62 0.036
985
c MLN065 Melanocytic Nevus Syndrome, Congenital 62 0.036
986
P LRS001 Larsen Syndrome 62 0.036
987
HYD038 Hydrops Fetalis, Nonimmune 62 0.036
988
P ORT004 Orthostatic Intolerance 62 0.036
989
c ANM038 Anemia, Autoimmune Hemolytic 62 0.036
990
CRC021 Carcinosarcoma 62 0.036
991
MSS001 Masa Syndrome 62 0.036
992
P DRM010 Dermatomyositis 61 0.036
993
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.036
994
WST001 West Syndrome 61 0.036
995
P ENC004 Encephalitis 61 0.036
996
CHR066 Chronic Fatigue Syndrome 61 0.036
997
c SPS215 Spastic Paraplegia 3, Autosomal Dominant 61 0.036
998
RCT015 Reactive Arthritis 61 0.036
999
P SJG008 Sjogren Syndrome 61 0.036
1000
GST033 Gestational Diabetes 61 0.036
1001
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.036
1002
NTH001 Netherton Syndrome 60 0.036
1003
PTN001 Patent Foramen Ovale 60 0.036
1004
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.036
1005
c JVN061 Juvenile Arthritis 60 0.036
1006
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.036
1007
c LYN004 Lynch Syndrome I 60 0.036
1008
LBR030 Leber Optic Atrophy 60 0.036
1009
RHM001 Rheumatic Fever 60 0.036
1010
P SNS001 Sensorineural Hearing Loss 60 0.036
1011
P GLY013 Glycogen Storage Disease 60 0.036
1012
P THL005 Thalassemia 60 0.036
1013
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.036
1014
ANT009 Antithrombin Iii Deficiency 59 0.036
1015
P MCR010 Microcephaly 59 0.036
1016
c DNG003 Dengue Disease 59 0.036
1017
PRN019 Perinatal Necrotizing Enterocolitis 59 0.036
1018
P PRD006 Prader-Willi Syndrome 59 0.036
1019
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 59 0.036
1020
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.036
1021
ALP097 Alopecia Universalis Congenita 59 0.036
1022
SRC027 Sarcoma, Synovial 58 0.036
1023
RNL024 Renal Glucosuria 58 0.036
1024
INC002 Inclusion Body Myositis 58 0.036
1025
PSD012 Pseudoachondroplasia 58 0.036
1026
RBS001 Rabies 58 0.036
1027
CRD132 Cardiac Conduction Defect 58 0.036
1028
BNG009 Benign Epilepsy with Centrotemporal Spikes 58 0.036
1029
EYD002 Eye Disease 58 0.036
1030
CRV038 Cervical Squamous Cell Carcinoma 58 0.036
1031
CHL028 Childhood Type Dermatomyositis 58 0.036
1032
LYM027 Lymphopenia 58 0.036
1033
EXT034 Extrinsic Allergic Alveolitis 58 0.036
1034
LNG108 Langerhans Cell Histiocytosis 58 0.036
1035
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.036
1036
P UVT001 Uveitis 57 0.036
1037
PMP006 Pemphigus Vulgaris, Familial 57 0.036
1038
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.036
1039
c CHR417 Chronic Graft Versus Host Disease 57 0.036
1040
c CHL119 Cholangitis, Primary Sclerosing 57 0.036
1041
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.036
1042
c LYS019 Loeys-Dietz Syndrome 1 57 0.036
1043
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.036
1044
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.036
1045
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 57 0.036
1046
APH001 Aphthous Stomatitis 57 0.036
1047
P PRV006 Pervasive Developmental Disorder 57 0.036
1048
c LKM070 Leukemia, Acute Monocytic 57 0.036
1049
CYT008 Cytomegalovirus Infection 57 0.036
1050
PLC005 Placental Insufficiency 57 0.036
1051
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.036
1052
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.036
1053
P ADL017 Adult T-Cell Leukemia 56 0.036
1054
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.036
1055
CMR002 Coumarin Resistance 56 0.036
1056
c SPS222 Spastic Paraplegia 20, Autosomal Recessive 56 0.036
1057
HPT046 Hepatic Veno-Occlusive Disease 56 0.036
1058
P MLT074 Multiple Endocrine Neoplasia 56 0.036
1059
ALL006 Allergic Asthma 56 0.036
1060
LBL001 Lobular Neoplasia 56 0.036
1061
EXF001 Exfoliation Syndrome 56 0.036
1062
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.036
1063
LMY014 Leiomyoma, Uterine 56 0.036
1064
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