Search results for Acetaminophen

1146 hits were found for Acetaminophen

# Family MCID Name MIFTS Score
1
ACT149 Acetaminophen Metabolism 35 4.179
2
PRC051 Paracetamol Poisoning 30 3.308
3
c ACT134 Acute Liver Failure 56 0.475
4
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.431
5
c PNS012 Paine Syndrome 61 0.423
6
PNG002 Pain Agnosia 51 0.400
7
OST012 Osteoarthritis 78 0.235
8
48X005 48,xyyy 39 0.235
9
P LVR013 Liver Disease 68 0.201
10
BCK006 Back Pain 42 0.190
11
P HDC001 Headache 57 0.184
12
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.184
13
P CHR345 Chronic Pain 44 0.179
14
CNS004 Constipation 58 0.176
15
c RHB024 Rhabdomyosarcoma 2 67 0.175
16
c MGR028 Migraine with or Without Aura 1 67 0.162
17
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.161
18
OCL069 Ocular Motor Apraxia 51 0.154
19
P KDN018 Kidney Disease 72 0.152
20
HPT004 Hepatic Coma 45 0.145
21
P TRN020 Turner Syndrome 67 0.144
22
ATX019 Ataxia with Vitamin E Deficiency 42 0.142
23
ADL002 Adult Syndrome 70 0.139
24
MTB004 Metabolic Acidosis 50 0.139
25
c ACT071 Acute Kidney Failure 60 0.137
26
P ART022 Arthritis 69 0.134
27
ALL026 Allergic Hypersensitivity Disease 62 0.127
28
HPT019 Hepatic Encephalopathy 60 0.127
29
SBC016 Subacute Delirium 44 0.126
30
P PTN014 Patent Ductus Arteriosus 1 60 0.124
31
P ALC033 Alcohol Use Disorder 58 0.124
32
ALC007 Alcohol Dependence 66 0.120
33
P ENC018 Encephalopathy 61 0.120
34
ILS001 Ileus 51 0.118
35
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.115
36
DPR016 Depression 63 0.113
37
P EXN002 Exanthem 57 0.111
38
STR067 Stroke, Ischemic 81 0.109
39
MNT002 Mental Depression 58 0.109
40
CHL079 Children's Interstitial Lung Disease 26 0.107
41
AST005 Asthma 76 0.105
42
P NRP001 Neuropathy 56 0.105
43
CRB039 Cerebrovascular Disease 67 0.103
44
FBR047 Fibromyalgia 58 0.103
45
MCN017 Meconium Ileus 52 0.103
46
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.100
47
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.096
48
ANX010 Anxiety 73 0.096
49
FTT001 Fatty Liver Disease 61 0.096
50
TNS005 Tonsillitis 57 0.096
51
CMM005 Common Cold 57 0.096
52
P MTH007 Methemoglobinemia 46 0.096
53
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.094
54
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.094
55
P URT039 Urticaria 58 0.094
56
P LCT001 Lactic Acidosis 51 0.094
57
PLP001 Pulpitis 49 0.094
58
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.094
59
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.091
60
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.091
61
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.091
62
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.091
63
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.091
64
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.091
65
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.091
66
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.091
67
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.091
68
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.091
69
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.091
70
DBT010 Diabetic Neuropathy 54 0.089
71
c INF145 Infantile Liver Failure Syndrome 1 50 0.089
72
P CNR004 Cone-Rod Dystrophy 2 73 0.086
73
c PRC016 Pre-Eclampsia 63 0.086
74
P CTR002 Cataract 60 0.086
75
MYF002 Myofascial Pain Syndrome 42 0.086
76
P ATS364 Autism 70 0.084
77
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.084
78
HYP266 Hypoxia 57 0.084
79
P SZR006 Seizure Disorder 56 0.084
80
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.084
81
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.084
82
P SLP006 Sleep Apnea 69 0.081
83
c MCR129 Microvascular Complications of Diabetes 1 66 0.081
84
LVR012 Liver Cirrhosis 62 0.081
85
P RHN004 Rhinitis 57 0.081
86
P SBS003 Substance Abuse 55 0.081
87
BRN071 Brain Injury 49 0.081
88
CYT002 Cytokine Deficiency 42 0.081
89
c HYP595 Hypertension, Essential 84 0.078
90
P HRT032 Heart Disease 75 0.078
91
P MYC007 Myocardial Infarction 70 0.078
92
c MCL013 Mucolipidosis Iv 66 0.078
93
P PNC044 Pancreatitis 61 0.078
94
P BCL017 B-Cell Lymphoma 58 0.078
95
P CLL015 Collagen Disease 47 0.078
96
ACT003 Acute Kidney Tubular Necrosis 45 0.078
97
c PRM038 Primary Agammaglobulinemia 44 0.078
98
P RSP003 Respiratory Failure 74 0.075
99
P HPT021 Hepatitis 67 0.075
100
CRP001 Carpal Tunnel Syndrome 67 0.075
101
APN008 Apnea, Obstructive Sleep 64 0.075
102
NTR005 Nutritional Deficiency Disease 62 0.075
103
ING001 Inguinal Hernia 60 0.075
104
ENT001 Enterocele 39 0.075
105
P CLR023 Colorectal Cancer 99 0.073
106
P RHM011 Rheumatoid Arthritis 80 0.073
107
LPT014 Leptin Deficiency or Dysfunction 74 0.073
108
DWN001 Down Syndrome 70 0.073
109
P THR014 Thrombocytopenia 67 0.073
110
DRM006 Dermatitis 61 0.073
111
SPN186 Spinal Cord Injury 60 0.073
112
RYS001 Reye Syndrome 51 0.073
113
OPD001 Opioid Abuse 46 0.073
114
MYL069 Myeloma, Multiple 85 0.069
115
ALL003 Allergic Rhinitis 67 0.069
116
c ATS007 Autism Spectrum Disorder 67 0.069
117
P ART023 Arthropathy 62 0.069
118
CHL068 Cholestasis 61 0.069
119
c ACT027 Acute Pancreatitis 60 0.069
120
VSL002 Visual Epilepsy 59 0.069
121
CMP010 Complex Regional Pain Syndrome 58 0.069
122
RFL001 Reflex Sympathetic Dystrophy 54 0.069
123
c VRL010 Viral Hepatitis 52 0.069
124
PLS009 Plasma Cell Neoplasm 51 0.069
125
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.069
126
GST020 Gastric Antral Vascular Ectasia 41 0.069
127
P BRS047 Breast Cancer 97 0.066
128
DFC004 Deficiency Anemia 70 0.066
129
P LYM118 Lymphoma 68 0.066
130
P LKM002 Leukemia 68 0.066
131
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.066
132
P DMN002 Dementia 66 0.066
133
HYP056 Hypoglycemia 66 0.066
134
KHL003 Kohlschutter-Tonz Syndrome 65 0.066
135
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.066
136
ALC006 Alcoholic Hepatitis 61 0.066
137
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.066
138
ISC004 Ischemia 58 0.066
139
ERY003 Erythema Multiforme 58 0.066
140
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.066
141
GLS018 Glass Syndrome 57 0.066
142
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.066
143
NPH009 Nephrolithiasis 55 0.066
144
P FBR031 Febrile Seizures 53 0.066
145
P ECL001 Eclampsia 50 0.066
146
ENT004 Enthesopathy 49 0.066
147
LYM019 Lymphosarcoma 46 0.066
148
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.066
149
CYT018 Cytochrome P450 2d6 Variant 27 0.066
150
P OVR042 Ovarian Cancer 88 0.063
151
SCK003 Sickle Cell Anemia 74 0.063
152
CNG034 Congestive Heart Failure 69 0.063
153
PRT037 Pertussis 65 0.063
154
CLF027 Cleft Palate, Isolated 64 0.063
155
P VSC007 Vascular Disease 63 0.063
156
P LPS004 Lupus Erythematosus 61 0.063
157
P KDN017 Kidney Cancer 60 0.063
158
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.063
159
AGN016 Aging 56 0.063
160
P DDN001 Duodenal Ulcer 52 0.063
161
ANG049 Angioedema Induced by Ace Inhibitors 40 0.063
162
FXD003 Fixed Drug Eruption 35 0.063
163
P ALZ034 Alzheimer Disease 88 0.059
164
c SYS001 Systemic Lupus Erythematosus 86 0.059
165
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.059
166
P OST002 Osteoporosis 74 0.059
167
SVR097 Severe Cutaneous Adverse Reaction 69 0.059
168
LYM133 Lymphoma, Hodgkin, Classic 69 0.059
169
P PNM007 Pneumonia 68 0.059
170
TTN003 Tetanus 65 0.059
171
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.059
172
c FNC043 Fanconi Anemia, Complementation Group E 62 0.059
173
DPH001 Diphtheria 60 0.059
174
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.059
175
P ANG015 Angioedema 57 0.059
176
AND020 Androgen Insensitivity, Partial 56 0.059
177
END086 End Stage Renal Disease 51 0.059
178
P SCK005 Sickle Cell Disease 50 0.059
179
DYS073 Dysphagia 50 0.059
180
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.059
181
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.059
182
ERY066 Erythema Multiforme Major 30 0.059
183
DQR001 De Quervain Disease 28 0.059
184
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.059
185
P LNG032 Lung Cancer 98 0.055
186
END057 Endometrial Cancer 74 0.055
187
c SPN225 Spondyloarthropathy 1 73 0.055
188
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.055
189
P HYP086 Hypothyroidism 69 0.055
190
P PRD008 Periodontitis 64 0.055
191
CHN016 Cohen Syndrome 63 0.055
192
c HPT003 Hepatitis a 62 0.055
193
LPP008 Lipoprotein Quantitative Trait Locus 62 0.055
194
TXC005 Toxic Shock Syndrome 62 0.055
195
HYP066 Hyperglycemia 61 0.055
196
P SNS001 Sensorineural Hearing Loss 60 0.055
197
CHC001 Chickenpox 60 0.055
198
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.055
199
HYP005 Hypokalemia 55 0.055
200
CRT017 Cartilage Disease 54 0.055
201
NNL006 Non-Alcoholic Steatohepatitis 54 0.055
202
TRM010 Traumatic Brain Injury 51 0.055
203
CHR005 Chorioamnionitis 51 0.055
204
OPT003 Opiate Dependence 50 0.055
205
P MGR001 Migraine Without Aura 49 0.055
206
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.055
207
LPT006 Leptin Receptor Deficiency 48 0.055
208
HDN002 Head Injury 46 0.055
209
P HYP265 Hypotonia 43 0.055
210
DRG002 Drug-Induced Hepatitis 43 0.055
211
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.055
212
c CHR682 Chronic Bilirubin Encephalopathy 39 0.055
213
P PRC031 Preeclampsia/eclampsia 1 38 0.055
214
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.051
215
P GRF003 Graft-Versus-Host Disease 72 0.051
216
P EPL164 Epilepsy 71 0.051
217
P MLN008 Melanoma 69 0.051
218
SKN019 Skin Melanoma 68 0.051
219
P CRD119 Cardiac Arrest 67 0.051
220
P SKN015 Skin Carcinoma 66 0.051
221
P PRS038 Personality Disorder 65 0.051
222
P ADL010 Adult Respiratory Distress Syndrome 65 0.051
223
P HYP750 Hypertriglyceridemia, Familial 62 0.051
224
APP008 Appendicitis 61 0.051
225
P MYL006 Myeloid Leukemia 60 0.051
226
LNG099 Lung Disease 60 0.051
227
IGR001 Ige Responsiveness, Atopic 59 0.051
228
SPN027 Spinal Stenosis 59 0.051
229
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.051
230
GLB001 Gilbert Syndrome 58 0.051
231
P INF032 Infertility 57 0.051
232
P PLV020 Pelvic Organ Prolapse 57 0.051
233
BRN056 Bronchopulmonary Dysplasia 57 0.051
234
DSS009 Disseminated Intravascular Coagulation 57 0.051
235
BLR008 Bilirubin Metabolic Disorder 57 0.051
236
HMR039 Hemorrhage, Intracerebral 57 0.051
237
PHR003 Pharyngitis 57 0.051
238
BRN004 Brain Edema 56 0.051
239
HPT022 Hepatoblastoma 56 0.051
240
ACT058 Active Peptic Ulcer Disease 55 0.051
241
INT075 Intracranial Hypertension 53 0.051
242
GST023 Gastric Ulcer 53 0.051
243
ART140 Arteries, Anomalies of 52 0.051
244
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.051
245
P ACT105 Acute Mountain Sickness 52 0.051
246
P MGR003 Migraine with Aura 52 0.051
247
SPN051 Spondylitis 51 0.051
248
c SVR005 Severe Pre-Eclampsia 50 0.051
249
47X002 47,xyy 49 0.051
250
OPD006 Opioid Addiction 48 0.051
251
RFR003 Refractive Error 43 0.051
252
DVR002 Diverticulitis 43 0.051
253
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.051
254
SPR126 Superior Semicircular Canal Dehiscence 40 0.051
255
c HMG029 Hemoglobin Se Disease 39 0.051
256
ABD010 Abdominal Wall Defect 36 0.051
257
INF009 Inflammatory Spondylopathy 31 0.051
258
HML018 Homologous Wasting Disease 22 0.051
259
P HPT023 Hepatocellular Carcinoma 100 0.047
260
MLR004 Malaria 81 0.047
261
IMM167 Immune Deficiency Disease 78 0.047
262
P SCH015 Schizophrenia 74 0.047
263
CRH001 Crohn's Disease 74 0.047
264
ULC004 Ulcerative Colitis 73 0.047
265
P MLT020 Multiple Sclerosis 72 0.047
266
P NRB001 Neuroblastoma 72 0.047
267
OTT002 Otitis Media 72 0.047
268
c LKM063 Leukemia, Chronic Myeloid 72 0.047
269
c EXD008 Exudative Vitreoretinopathy 1 71 0.047
270
c CHR684 Chronic Kidney Disease 70 0.047
271
P OCL013 Oculodentodigital Dysplasia 69 0.047
272
P LKM062 Leukemia, Acute Lymphoblastic 69 0.047
273
P NRV007 Nervous System Disease 66 0.047
274
P DBT009 Diabetes Mellitus 64 0.047
275
MSC007 Muscle Hypertrophy 64 0.047
276
P NTR004 Neutropenia 63 0.047
277
SKN016 Skin Disease 63 0.047
278
TRN015 Transient Cerebral Ischemia 63 0.047
279
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.047
280
HMT002 Hematologic Cancer 62 0.047
281
P VSC011 Vasculitis 62 0.047
282
MDD011 Mood Disorder 62 0.047
283
P SCL018 Scoliosis 60 0.047
284
PRT058 Pure Autonomic Failure 59 0.047
285
ANR040 Aneurysm 59 0.047
286
P PRP019 Peripheral Nervous System Disease 58 0.047
287
P GLL020 Gallbladder Disease 57 0.047
288
c ACT075 Acute Myocardial Infarction 57 0.047
289
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.047
290
GST050 Gastrointestinal System Disease 56 0.047
291
P GST044 Gastritis 56 0.047
292
P AGN002 Agnosia 55 0.047
293
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.047
294
PRP030 Purpura 54 0.047
295
PLM010 Pulmonary Edema 54 0.047
296
BRD004 Borderline Personality Disorder 53 0.047
297
MTN003 Motion Sickness 53 0.047
298
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.047
299
P RCT021 Rectum Cancer 52 0.047
300
RDC002 Radiculopathy 50 0.047
301
STM007 Stomatitis 50 0.047
302
URM002 Uremia 49 0.047
303
INT067 Interstitial Nephritis 48 0.047
304
PYL006 Pyloric Stenosis 48 0.047
305
CLN045 Colonic Benign Neoplasm 46 0.047
306
CYN002 Cyanosis, Transient Neonatal 45 0.047
307
LWC001 Low Compliance Bladder 43 0.047
308
IDP070 Idiopathic Scoliosis 42 0.047
309
DBT002 Diabetic Autonomic Neuropathy 41 0.047
310
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.047
311
OVR094 Ovarian Epithelial Cancer 38 0.047
312
c SYS043 Systemic Lupus Erythematosus 1 38 0.047
313
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.047
314
HPT085 Hepatitis, Fulminant Viral 32 0.047
315
DVR001 Diverticulitis of Colon 25 0.047
316
ESP021 Esophageal Cancer 90 0.042
317
SVR004 Severe Combined Immunodeficiency 73 0.042
318
HMN044 Human Immunodeficiency Virus Type 1 71 0.042
319
CRB037 Cerebral Palsy 69 0.042
320
BRN024 Bronchitis 68 0.042
321
P HYP098 Hypereosinophilic Syndrome 67 0.042
322
OST159 Osteogenic Sarcoma 66 0.042
323
PPL049 Papillon-Lefevre Syndrome 65 0.042
324
IRR002 Irritable Bowel Syndrome 65 0.042
325
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.042
326
P GLM045 Glioma 63 0.042
327
P HML002 Hemolytic Anemia 63 0.042
328
P CRN300 Coronary Heart Disease 1 63 0.042
329
END041 Endometrial Adenocarcinoma 63 0.042
330
c ATM011 Autoimmune Hepatitis 63 0.042
331
c HPT001 Hepatitis C 62 0.042
332
MSL001 Measles 62 0.042
333
OSS012 Osseous Heteroplasia, Progressive 61 0.042
334
ACQ007 Acquired Immunodeficiency Syndrome 60 0.042
335
PLM033 Pulmonary Embolism 59 0.042
336
PRN019 Perinatal Necrotizing Enterocolitis 59 0.042
337
c ACT073 Acute Leukemia 58 0.042
338
BRS051 Breast Disease 58 0.042
339
THR024 Thrombosis 57 0.042
340
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.042
341
VSC002 Vascular Dementia 57 0.042
342
MCS002 Mucositis 56 0.042
343
c BCT007 Bacterial Meningitis 55 0.042
344
DFF005 Diffuse Large B-Cell Lymphoma 55 0.042
345
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.042
346
AMN003 Amnestic Disorder 54 0.042
347
GST037 Gastroparesis 54 0.042
348
HMS001 Hemosiderosis 54 0.042
349
LYM040 Lymphoblastic Lymphoma 54 0.042
350
GST009 Gastroschisis 53 0.042
351
c HPT007 Hepatitis E 53 0.042
352
LMY002 Leiomyoma 52 0.042
353
SPS003 Spastic Diplegia 51 0.042
354
P HMP007 Hemophilia 51 0.042
355
AVD001 Avoidant Personality Disorder 51 0.042
356
ENT011 Enterocolitis 51 0.042
357
SPN019 Spondylolisthesis 51 0.042
358
CRT013 Carotid Stenosis 50 0.042
359
NTR046 Neutrophil Migration 50 0.042
360
STM006 Stomach Disease 47 0.042
361
PRP017 Periapical Periodontitis 46 0.042
362
GLL048 Glial Tumor 45 0.042
363
P OCY003 Oocyte Maturation Defect 1 45 0.042
364
P RRH023 Rare Hereditary Hemochromatosis 41 0.042
365
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.042
366
SWL001 Swallowing Disorders 38 0.042
367
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.042
369
c CHR064 Chronic Monocytic Leukemia 33 0.042
370
PST092 Posttransplant Acute Limbic Encephalitis 29 0.042
371
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.036
372
c LKM061 Leukemia, Acute Myeloid 84 0.036
373
CYS001 Cystic Fibrosis 81 0.036
374
P BLD134 Bladder Cancer 79 0.036
375
CNN003 Conn's Syndrome 79 0.036
376
INS024 Insulin-Like Growth Factor I 79 0.036
377
GST019 Gastrointestinal Stromal Tumor 78 0.036
378
GLB015 Glioblastoma Multiforme 75 0.036
379
c THR092 Thrombophilia Due to Thrombin Defect 73 0.036
380
PRP027 Peripheral Vascular Disease 71 0.036
381
P FRG001 Fragile X Syndrome 70 0.036
382
c INF071 Inflammatory Bowel Disease 1 67 0.036
383
PSY004 Psychotic Disorder 67 0.036
384
ANG054 Angina Pectoris 66 0.036
385
P ATR011 Atrial Fibrillation 66 0.036
386
P MNN013 Meningitis 66 0.036
387
c SML038 Small Cell Cancer of the Lung 65 0.036
388
c FML001 Familial Atrial Fibrillation 65 0.036
389
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.036
390
NRM005 Neuromuscular Disease 64 0.036
391
P ADN016 Adenocarcinoma 64 0.036
392
INT146 Intervertebral Disc Disease 63 0.036
393
c ACT068 Acute Cystitis 63 0.036
394
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.036
395
P PSR002 Psoriasis 62 0.036
396
INT066 Interstitial Lung Disease 60 0.036
397
P VNT002 Ventricular Septal Defect 60 0.036
398
P RBL001 Rubella 59 0.036
399
c HPT016 Hepatitis B 59 0.036
400
CHL123 Chlamydia 59 0.036
401
P PRD006 Prader-Willi Syndrome 59 0.036
402
ADN018 Adenoma 59 0.036
403
PPT005 Peptic Ulcer Disease 59 0.036
404
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.036
405
NWB001 Newborn Respiratory Distress Syndrome 58 0.036
406
DSS008 Disease of Mental Health 58 0.036
407
P MMP001 Mumps 58 0.036
408
P GLM007 Glomerulonephritis 57 0.036
409
CHL067 Cholecystitis 57 0.036
410
APH001 Aphthous Stomatitis 57 0.036
411
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.036
412
HPT046 Hepatic Veno-Occlusive Disease 56 0.036
413
LMY014 Leiomyoma, Uterine 56 0.036
414
ADN027 Adenomyosis 56 0.036
415
BCT022 Bacterial Infectious Disease 56 0.036
416
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.036
417
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.036
418
P ANT006 Antiphospholipid Syndrome 55 0.036
419
P MYP006 Myopia 55 0.036
420
P STR020 Strabismus 55 0.036
421
END040 Endogenous Depression 55 0.036
422
TND005 Tendinitis 54 0.036
423
P INF037 Inflammatory Bowel Disease 54 0.036
424
HLL004 Hellp Syndrome 54 0.036
425
PNC001 Pancytopenia 54 0.036
426
PRS045 Prostatic Hypertrophy 53 0.036
427
BRN038 Bronchial Disease 53 0.036
428
P HMR003 Hemorrhagic Disease 53 0.036
429
NRT001 Neurotic Disorder 53 0.036
430
PRP080 Peripheral Artery Disease 53 0.036
431
PST011 Pustulosis of Palm and Sole 52 0.036
432
c PNC106 Pancreatic Agenesis 1 51 0.036
433
LNG031 Lung Benign Neoplasm 51 0.036
434
P HYP040 Hypospadias 51 0.036
435
SKN013 Skin Benign Neoplasm 51 0.036
436
HYP781 Hypoascorbemia 51 0.036
437
HMG002 Hemoglobinuria 50 0.036
438
BLD053 Blood Platelet Disease 49 0.036
439
CHL004 Cholelithiasis 49 0.036
440
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.036
441
PNC034 Pancreas Disease 48 0.036
442
DGN001 Degenerative Disc Disease 48 0.036
443
PLC007 Placental Abruption 48 0.036
444
P DPY001 Dupuytren Contracture 48 0.036
445
DRG003 Drug Dependence 47 0.036
446
GLT007 Glutathione Synthetase Deficiency 47 0.036
447
SPN020 Spondylosis 46 0.036
448
UMB002 Umbilical Hernia 46 0.036
449
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.036
450
MYF001 Myofibroma 45 0.036
451
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.036
452
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.036
453
NSP002 Nasopharyngitis 43 0.036
454
PLY068 Polysubstance Abuse 43 0.036
455
HMP009 Haemophilus Influenzae 43 0.036
456
MCH006 Mechanical Strabismus 42 0.036
457
RDN001 Reading Disorder 40 0.036
458
P INT260 Intracranial Berry Aneurysm 39 0.036
459
FML039 Female Reproductive System Disease 39 0.036
460
SPP003 Suppurative Periapical Periodontitis 34 0.036
461
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.036
462
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.036
463
c ALC016 Alcohol Sensitivity, Acute 31 0.036
464
RSP007 Respiratory Distress Syndrome, Infant 30 0.036
465
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.036
466
c DMN005 Diamond-Blackfan Anemia 2 25 0.036
467
INT053 Intracranial Vasospasm 24 0.036
468
P PRS040 Prostate Cancer 97 0.030
469
P PNC035 Pancreatic Cancer 84 0.030
470
c NRF023 Neurofibromatosis, Type Ii 80 0.030
471
P LKM071 Leukemia, Chronic Lymphocytic 79 0.030
472
PFF001 Pfeiffer Syndrome 79 0.030
473
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.030
474
P PRK057 Parkinson Disease, Late-Onset 78 0.030
475
c NRF024 Neurofibromatosis, Type I 77 0.030
476
CRV035 Cervical Cancer 76 0.030
477
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.030
478
ADR007 Adrenoleukodystrophy 75 0.030
479
BRN028 Brain Cancer 74 0.030
480
c HMC039 Hemochromatosis, Type 1 74 0.030
481
P RTN024 Retinoblastoma 73 0.030
482
P PHC003 Pheochromocytoma 71 0.030
483
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.030
484
P SRC025 Sarcoidosis 1 70 0.030
485
MYL009 Myelodysplastic Syndrome 70 0.030
486
c GLY008 Glycogen Storage Disease Ii 70 0.030
487
P MYP004 Myopathy 70 0.030
488
ART016 Aortic Aneurysm 69 0.030
489
EWN003 Ewing Sarcoma 69 0.030
490
MNT001 Mantle Cell Lymphoma 69 0.030
491
P SYS005 Systemic Scleroderma 68 0.030
492
P INF038 Influenza 68 0.030
493
P MJR001 Major Depressive Disorder 68 0.030
494
HYL004 Hyaline Fibromatosis Syndrome 67 0.030
495
GST092 Gastroesophageal Reflux 67 0.030
496
P PLM037 Pulmonary Hypertension 67 0.030
497
PRT010 Parathyroid Carcinoma 67 0.030
498
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.030
499
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.030
500
P DRM053 Dermatitis, Atopic 66 0.030
501
P CNJ013 Conjunctivitis 65 0.030
502
P MTR014 Motor Neuron Disease 65 0.030
503
PND002 Pendred Syndrome 65 0.030
504
ATH013 Atherosclerosis Susceptibility 65 0.030
505
c DBT099 Diabetes Mellitus, Type I 65 0.030
506
P THY023 Thymoma 65 0.030
507
NRF007 Neurofibroma 64 0.030
508
c JVN010 Juvenile Rheumatoid Arthritis 64 0.030
509
GT001 Gout 64 0.030
510
DGR001 Digeorge Syndrome 64 0.030
511
PLM031 Poliomyelitis 64 0.030
512
LYM017 Lyme Disease 64 0.030
513
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.030
514
ANR007 Anorexia Nervosa 63 0.030
515
P END044 Endometriosis 63 0.030
516
CLT003 Colitis 62 0.030
517
c BRN108 Branchiootic Syndrome 1 62 0.030
518
P SPN046 Spinal Muscular Atrophy 62 0.030
519
P TRC086 Trichohepatoenteric Syndrome 1 62 0.030
520
ATM095 Autoimmune Disease 62 0.030
521
P PRM006 Primary Biliary Cirrhosis 62 0.030
522
PSR001 Psoriatic Arthritis 61 0.030
523
P INT143 Interstitial Cystitis 61 0.030
524
INT002 Intermittent Claudication 61 0.030
525
c SCL052 Scleroderma, Familial Progressive 61 0.030
526
HRP004 Herpes Zoster 60 0.030
527
P NPH012 Nephrotic Syndrome 60 0.030
528
PNM010 Pneumothorax, Primary Spontaneous 60 0.030
529
VRC005 Varicose Veins 60 0.030
530
P GLY013 Glycogen Storage Disease 60 0.030
531
P THL005 Thalassemia 60 0.030
532
P MYC008 Myocarditis 59 0.030
533
PRT013 Portal Hypertension 59 0.030
534
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.030
535
P BND020 Bone Disease 59 0.030
536
THY029 Thyroid Carcinoma 59 0.030
537
c DNG003 Dengue Disease 59 0.030
538
P SLP005 Sleep Disorder 59 0.030
539
P CYS018 Cystitis 59 0.030
540
BRN002 Bronchiolitis 59 0.030
541
CNT047 Contact Dermatitis 58 0.030
542
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.030
543
P CND004 Candidiasis 58 0.030
544
PMP006 Pemphigus Vulgaris, Familial 57 0.030
545
c CHR417 Chronic Graft Versus Host Disease 57 0.030
546
IRN002 Iron Metabolism Disease 57 0.030
547
THY122 Thyroid Gland Cancer 57 0.030
548
P END033 Endocarditis 57 0.030
549
P FCL005 Focal Segmental Glomerulosclerosis 57 0.030
550
P BPL003 Bipolar Disorder 56 0.030
551
PNM008 Pneumothorax 56 0.030
552
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.030
553
CMR002 Coumarin Resistance 56 0.030
554
SPN041 Spinal Cord Disease 56 0.030
555
GNR004 Generalized Anxiety Disorder 56 0.030
556
ALL010 Allergic Contact Dermatitis 56 0.030
557
MTH009 Mouth Disease 56 0.030
558
P NRF002 Neurofibromatosis 56 0.030
559
ORL005 Oral Candidiasis 56 0.030
560
P ATR001 Atrioventricular Septal Defect 55 0.030
561
P DRR001 Diarrhea 55 0.030
562
P HYP076 Hyperthyroidism 55 0.030
563
P PMP001 Pemphigus 54 0.030
564
P ALP008 Alopecia 54 0.030
565
VLC001 Velocardiofacial Syndrome 54 0.030
566
CLL003 Cellulitis 54 0.030
567
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.030
568
P HMC002 Homocystinuria 53 0.030
569
CRH005 Crohn's Colitis 53 0.030
570
MST005 Mastitis 53 0.030
571
P HML001 Hemolytic-Uremic Syndrome 53 0.030
572
INF034 Infective Endocarditis 53 0.030
573
P SHR001 Short Bowel Syndrome 53 0.030
574
CLF001 Cleft Lip 53 0.030
575
GTR002 Goiter 53 0.030
576
c FML008 Familial Retinoblastoma 53 0.030
577
c GLL024 Gallbladder Disease 1 53 0.030
578
c PSR017 Psoriasis 2 53 0.030
579
THY030 Thyroid Gland Disease 52 0.030
580
P MSC003 Muscular Atrophy 52 0.030
581
c THY107 Thymoma, Familial 52 0.030
582
c PSR023 Psoriasis 1 52 0.030
583
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.030
584
THR004 Thrombocytosis 51 0.030
585
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.030
586
KRT009 Keratosis 51 0.030
587
HND002 Hand, Foot and Mouth Disease 51 0.030
588
P AST007 Astrocytoma 51 0.030
589
BHR001 Behr Syndrome 51 0.030
590
PST021 Postpartum Depression 50 0.030
591
HPT014 Hepatorenal Syndrome 50 0.030
592
P ESN008 Eosinophilic Pneumonia 50 0.030
593
HRT011 Heart Septal Defect 50 0.030
594
HYP017 Hypophosphatemia 50 0.030
595
HDR003 Hidradenitis 49 0.030
596
P MST002 Mast-Cell Leukemia 49 0.030
597
BNR002 Bone Resorption Disease 48 0.030
598
SPL018 Splenomegaly 48 0.030
599
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.030
600
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.030
601
AST006 Astigmatism 47 0.030
602
c PSR032 Psoriasis 11 47 0.030
603
RTC005 Reticulosarcoma 47 0.030
604
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.030
605
ANL022 Anal Fistula 46 0.030
606
TST014 Testicular Cancer 46 0.030
607
SMT001 Somatization Disorder 46 0.030
608
ADR040 Adrenal Gland Pheochromocytoma 46 0.030
609
P HMR005 Hemorrhoid 46 0.030
610
c MLG068 Malignant Glioma 46 0.030
611
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.030
612
RTR008 Root Resorption 45 0.030
613
CRB004 Cerebral Artery Occlusion 45 0.030
614
IMM136 Immune System Disease 45 0.030
615
URL001 Urolithiasis 45 0.030
616
HRP001 Herpangina 45 0.030
617
CLL014 Cll/sll 45 0.030
618
PRT030 Parathyroid Gland Disease 45 0.030
619
ATN004 Autonomic Neuropathy 45 0.030
620
ANS012 Anus Disease 45 0.030
621
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.030
622
c CHR579 Chiari Malformation Type Ii 44 0.030
623
PTT037 Pituitary Tumors 44 0.030
624
PLX002 Plexiform Neurofibroma 44 0.030
625
PPL001 Papillary Adenoma 44 0.030
626
c HRD173 Hereditary Late-Onset Parkinson Disease 44 0.030
627
DMP001 Dumping Syndrome 44 0.030
628
CVD001 Covid-19 44 0.030
629
TND004 Tendinopathy 43 0.030
630
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.030
631
URT037 Urethral Stricture 43 0.030
632
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 43 0.030
633
STL007 Steel Syndrome 43 0.030
634
TRP009 Triple X Syndrome 42 0.030
635
PNM013 Pneumococcal Meningitis 42 0.030
636
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.030
637
c PSR028 Psoriasis 7 42 0.030
638
DRG024 Drug Allergy 42 0.030
639
P CHR342 Chiari Malformation 41 0.030
640
DNT006 Dental Pulp Necrosis 41 0.030
641
DFF003 Diffuse Scleroderma 41 0.030
642
c PSR018 Psoriasis 13 41 0.030
643
c MJR024 Major Affective Disorder 9 41 0.030
644
PRS063 Paresthesia 41 0.030
645
ALC005 Alcoholic Pancreatitis 40 0.030
646
CRD005 Cardia Cancer 40 0.030
647
ADN067 Adenoid Hypertrophy 39 0.030
648
c MJR022 Major Affective Disorder 8 38 0.030
649
INF039 Infratentorial Cancer 38 0.030
650
BLN010 Balanitis 37 0.030
651
PHM001 Phimosis 37 0.030
652
CHL013 Cholecystolithiasis 37 0.030
653
ACL001 Acalculous Cholecystitis 35 0.030
654
RFR013 Refractory Celiac Disease 35 0.030
655
KDN001 Kidney Cortex Necrosis 34 0.030
656
DDN004 Duodenogastric Reflux 33 0.030
657
c PRS136 Prostate Cancer, Hereditary, 6 33 0.030
658
c PRS130 Prostate Cancer, Hereditary, 8 32 0.030
659
PTL002 Patellofemoral Pain Syndrome 31 0.030
660
PLR005 Pleuropneumonia 31 0.030
661
ALV001 Alveolar Periostitis 30 0.030
662
FNT004 Fainting 30 0.030
663
PRP013 Paraphimosis 30 0.030
664
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.030
665
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.030
666
PTL003 Patellar Tendinitis 26 0.030
667
HRP008 Herpes Simiae 25 0.030
668
ANT078 Antipyrine Metabolism 24 0.030
669
HDG004 Hodgkin's Granuloma 23 0.030
670
HDG006 Hodgkin's Paragranuloma 22 0.030
671
HPS001 Hip Subluxation 20 0.030
672
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.021
673
NRL016 Neural Tube Defects 82 0.021
674
P ATX030 Ataxia-Telangiectasia 82 0.021
675
P GLM040 Glioma Susceptibility 1 81 0.021
676
P MDL005 Medulloblastoma 77 0.021
677
MRF001 Marfan Syndrome 77 0.021
678
c ATR087 Atrial Standstill 1 75 0.021
679
P APL001 Aplastic Anemia 74 0.021
680
c HYP836 Hypercholesterolemia, Familial, 1 73 0.021
681
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.021
682
MSC157 Muscular Dystrophy, Duchenne Type 72 0.021
683
c HPT073 Hepatitis C Virus 72 0.021
684
P HNT016 Huntington Disease 72 0.021
685
MYL005 Myelofibrosis 70 0.021
686
c GCH015 Gaucher Disease, Type I 70 0.021
687
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.021
688
PLM001 Pulmonary Tuberculosis 69 0.021
689
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.021
690
P ANG001 Angelman Syndrome 69 0.021
691
P CRN037 Craniosynostosis 68 0.021
692
P MYC084 Mycobacterium Tuberculosis 1 68 0.021
693
c BSL007 Basal Cell Carcinoma 68 0.021
694
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.021
695
c HMP004 Hemophilia B 68 0.021
696
CNN005 Connective Tissue Disease 68 0.021
697
RCK004 Rickets 68 0.021
698
P FRN006 Frontotemporal Dementia 68 0.021
699
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.021
700
FCT007 Factor Vii Deficiency 67 0.021
701
P OLG002 Oligodendroglioma 67 0.021
702
BRK010 Burkitt Lymphoma 67 0.021
703
P FLL037 Follicular Lymphoma 67 0.021
704
c HMP029 Hemophilia a 67 0.021
705
P CLC063 Celiac Disease 1 66 0.021
706
GLL008 Gilles De La Tourette Syndrome 66 0.021
707
P MSC005 Muscular Dystrophy 66 0.021
708
ART001 Arterial Tortuosity Syndrome 66 0.021
709
P HYD006 Hydrocephalus 66 0.021
710
MYL031 Myeloproliferative Neoplasm 66 0.021
711
P HRS035 Hirschsprung Disease 1 65 0.021
712
P ART005 Arteriovenous Malformation 65 0.021
713
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.021
714
DMN031 Dementia, Lewy Body 65 0.021
715
SRC014 Sarcoma 65 0.021
716
GRN037 Granulomatosis with Polyangiitis 65 0.021
717
P CTS001 Cutis Laxa 65 0.021
718
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.021
719
KWS002 Kawasaki Disease 65 0.021
720
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.021
721
CLN015 Colon Adenocarcinoma 65 0.021
722
PRT036 Peritonitis 64 0.021
723
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.021
724
CTR172 Citrullinemia, Classic 64 0.021
725
P RHB003 Rhabdomyosarcoma 63 0.021
726
P GCH001 Gaucher's Disease 63 0.021
727
P ANR048 Aniridia 1 63 0.021
728
P HYP069 Hyperparathyroidism 63 0.021
729
PLG002 Plague 63 0.021
730
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.021
731
HYP780 Hypoadrenocorticism, Familial 63 0.021
732
P LMY004 Leiomyosarcoma 63 0.021
733
RHB001 Rhabdoid Cancer 63 0.021
734
BDD001 Budd-Chiari Syndrome 63 0.021
735
c LCL006 Localized Scleroderma 62 0.021
736
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.021
737
c SVR001 Severe Acute Respiratory Syndrome 62 0.021
738
P BCK002 Beckwith-Wiedemann Syndrome 62 0.021
739
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 0.021
740
P ACR001 Aicardi-Goutieres Syndrome 62 0.021
741
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.021
742
CHR001 Churg-Strauss Syndrome 61 0.021
743
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.021
744
CHR066 Chronic Fatigue Syndrome 61 0.021
745
WLD007 Waldenstroem's Macroglobulinemia 61 0.021
746
P SJG008 Sjogren Syndrome 61 0.021
747
VRL011 Viral Infectious Disease 61 0.021
748
TTH002 Tooth Agenesis 60 0.021
749
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.021
750
TRG002 Trigeminal Neuralgia 60 0.021
751
c JVN061 Juvenile Arthritis 60 0.021
752
P BNG030 Benign Ependymoma 60 0.021
753
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.021
754
ACN002 Acanthosis Nigricans 60 0.021
755
P ALP009 Alopecia Areata 60 0.021
756
ETN001 Eating Disorder 60 0.021
757
STT001 Status Epilepticus 60 0.021
758
P CHR285 Chronic Myelomonocytic Leukemia 60 0.021
759
P OPT006 Optic Nerve Disease 60 0.021
760
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 59 0.021
761
P LYM033 Lymphoproliferative Syndrome 59 0.021
762
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.021
763
P MLN069 Melanoma, Uveal 59 0.021
764
P BRS044 Breast Adenocarcinoma 59 0.021
765
GRD007 Grade Iii Astrocytoma 59 0.021
766
P GLL022 Guillain-Barre Syndrome 59 0.021
767
GST045 Gastroenteritis 59 0.021
768
P ANP001 Anaplastic Large Cell Lymphoma 58 0.021
769
PST028 Post-Traumatic Stress Disorder 58 0.021
770
CRD132 Cardiac Conduction Defect 58 0.021
771
P BNC003 Bone Cancer 58 0.021
772
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 58 0.021
773
c DWL002 Dowling-Degos Disease 1 58 0.021
774
LYM027 Lymphopenia 58 0.021
775
P MYM013 Moyamoya Disease 1 57 0.021
776
LYM021 Lymphadenitis 57 0.021
777
c MST023 Mesothelioma, Malignant 57 0.021
778
P CRD246 Cardiovascular System Disease 57 0.021
779
P CTR177 Citrullinemia, Type Ii, Adult-Onset 57 0.021
780
INT303 Intracranial Hypertension, Idiopathic 57 0.021
781
c SML009 Small Intestine Adenocarcinoma 57 0.021
782
AYM001 Ayme-Gripp Syndrome 57 0.021
783
P PYL005 Pyelonephritis 56 0.021
784
P ADL017 Adult T-Cell Leukemia 56 0.021
785
P CHN012 Chondrosarcoma 56 0.021
786
TRN018 Transitional Cell Carcinoma 56 0.021
787
ALL006 Allergic Asthma 56 0.021
788
PLS011 Plasmacytoma 56 0.021
789
SFT003 Soft Tissue Sarcoma 56 0.021
790
PRS047 Prostatitis 56 0.021
791
ISL001 Islet Cell Tumor 56 0.021
792
ANN002 Anencephaly 56 0.021
793
NRL004 Neuroleptic Malignant Syndrome 56 0.021
794
HMG005 Hemoglobinopathy 56 0.021
795
EMB004 Embryonal Carcinoma 56 0.021
796
P HYP024 Hypoparathyroidism 56 0.021
797
MRD002 Marden-Walker Syndrome 56 0.021
798
c FML035 Familial Hyperlipidemia 55 0.021
799
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.021
800
c SPN395 Spinal Muscular Atrophy, Type Ii 55 0.021
801
P PTT006 Pituitary Adenoma 55 0.021
802
CHR100 Chronic Ulcer of Skin 55 0.021
803
P ALP106 Alport Syndrome 1, X-Linked 55 0.021
804
JVN009 Juvenile Pilocytic Astrocytoma 55 0.021
805
P DBT005 Diabetes Insipidus 55 0.021
806
INT007 Intermediate Coronary Syndrome 55 0.021
807
HRY003 Hairy Cell Leukemia 55 0.021
808
CLF004 Cleft Lip/palate 54 0.021
809
SYN007 Synovitis 54 0.021
810
HYP060 Hyperinsulinism 54 0.021
811
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.021
812
TRD006 Tardive Dyskinesia 54 0.021
813
GLS001 Gliosarcoma 54 0.021
814
GLC003 Glucose Intolerance 54 0.021
815
PRT082 Preterm Premature Rupture of the Membranes 54 0.021
816
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.021
817
P RST001 Restless Legs Syndrome 54 0.021
818
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.021
819
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.021
820
CLL010 Cellular Ependymoma 54 0.021
821
THR013 Thoracic Outlet Syndrome 54 0.021
822
PRC013 Pericarditis 54 0.021
823
P ART021 Arteriosclerosis 54 0.021
824
P LTR001 Lateral Sclerosis 54 0.021
825
ADR049 Adrenal Hypoplasia, Congenital 54 0.021
826
PTT009 Pituitary Gland Disease 54 0.021
827
P TRM003 Tremor 54 0.021
828
CLR030 Clear Cell Renal Cell Carcinoma 53 0.021
829
MMM001 Mammary Paget's Disease 53 0.021
830
c SPN394 Spinal Muscular Atrophy, Type Iii 53 0.021
831
PST046 Post-Transplant Lymphoproliferative Disease 53 0.021
832
PLS016 Plasma Cell Leukemia 53 0.021
833
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.021
834
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.021
835
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.021
836
c XNT010 Xanthinuria, Type I 53 0.021
837
SPN035 Spindle Cell Sarcoma 53 0.021
838
TXC002 Toxic Encephalopathy 53 0.021
839
P INT068 Intestinal Disease 53 0.021
840
P RTN018 Retinal Disease 53 0.021
841
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.021
842
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.021
843
ACR041 Acromelic Frontonasal Dysostosis 52 0.021
844
PRS030 Persistent Fetal Circulation Syndrome 52 0.021
845
GLM004 Gliomatosis Cerebri 52 0.021
846
PLS007 Plasmodium Falciparum Malaria 52 0.021
847
MRG003 Marginal Zone B-Cell Lymphoma 52 0.021
848
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.021
849
PTH003 Pathologic Nystagmus 52 0.021
850
HYP014 Hyperuricemia 52 0.021
851
c BRL011 Bare Lymphocyte Syndrome, Type I 52 0.021
852
TLN003 Telangiectasis 52 0.021
853
DSM007 Desmoplastic Small Round Cell Tumor 52 0.021
854
c SPN393 Spinal Muscular Atrophy, Type I 52 0.021
855
c ACT135 Acute Graft Versus Host Disease 52 0.021
856
P BRN035 Brain Stem Glioma 52 0.021
857
PRV004 Periventricular Leukomalacia 52 0.021
859
P SPP010 Suppressor of Tumorigenicity 3 51 0.021
860
MCR088 Microscopic Polyangiitis 51 0.021
861
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.021
862
ESP002 Esophageal Varix 51 0.021
863
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.021
864
NRM004 Neuroma 51 0.021
865
SPL004 Splenic Marginal Zone Lymphoma 51 0.021
866
BLL003 Bell's Palsy 51 0.021
867
FBR008 Fibrillary Astrocytoma 51 0.021
868
HYP074 Hypersensitivity Vasculitis 51 0.021
869
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.021
870
CRD229 Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism 51 0.021
871
PNM005 Pneumonic Plague 51 0.021
872
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.021
873
INT071 Intestinal Perforation 51 0.021
874
GNT002 Giant Cell Glioblastoma 50 0.021
875
SCH012 Schizoaffective Disorder 50 0.021
876
PLR008 Pleurisy 50 0.021
877
P OVR082 Overgrowth Syndrome 50 0.021
878
BRX001 Bruxism 50 0.021
879
RSP006 Respiratory System Disease 50 0.021
880
P SML016 Small Intestine Cancer 50 0.021
881
FSC004 Fasciitis 50 0.021
882
c THR071 Thrombocytopenia 1 50 0.021
883
PLC008 Placenta Disease 50 0.021
884
P PNB001 Pineoblastoma 50 0.021
885
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.021
886
OCL022 Ocular Melanoma 50 0.021
887
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 50 0.021
888
RBF001 Riboflavin Deficiency 49 0.021
889
ATY042 Atypical Chronic Myeloid Leukemia 49 0.021
890
c CHR418 Chronic Leukemia 49 0.021
891
PPL021 Papilledema 49 0.021
892
CHL018 Childhood Medulloblastoma 49 0.021
893
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.021
894
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.021
895
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.021
896
AMB002 Amblyopia 49 0.021
897
CCN002 Cocaine Abuse 49 0.021
898
MCR004 Macroglobulinemia 49 0.021
899
c FLL041 Follicular Lymphoma 1 49 0.021
900
VCC001 Vaccinia 49 0.021
901
SBP001 Subependymal Giant Cell Astrocytoma 49 0.021
902
c 46X049 46,xy Sex Reversal 2 48 0.021
903
c BCT013 Bacterial Pneumonia 48 0.021
904
c DSB006 Desbuquois Dysplasia 1 48 0.021
905
SBS004 Substance Dependence 48 0.021
906
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.021
907
c NPH049 Nephrotic Syndrome, Type 2 48 0.021
908
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.021
909
VTM033 Vitamin K Deficiency Bleeding 48 0.021
910
PLM035 Pulmonary Eosinophilia 48 0.021
911
P LYM024 Lymphatic System Disease 48 0.021
912
BNN003 Bone Inflammation Disease 48 0.021
913
HYP025 Hyperphosphatemia 48 0.021
914
P MRC003 Mercury Poisoning 48 0.021
915
HLX001 Helix Syndrome 47 0.021
916
GRM005 Germ Cell Cancer 47 0.021
917
PRL017 Prolymphocytic Leukemia 47 0.021
918
CLF056 Cleft Lip with or Without Cleft Palate 47 0.021
919
LRY029 Laryngomalacia 47 0.021
920
CLN019 Colonic Disease 47 0.021
921
P BLR006 Biliary Tract Disease 47 0.021
922
RNL077 Renal Fibrosis 47 0.021
923
ACT055 Actinomycosis 47 0.021
924
ACT084 Acute Stress Disorder 47 0.021
925
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.021
926
PGT003 Paget Disease, Extramammary 47 0.021
927
KRT002 Keratomalacia 47 0.021
928
LYM012 Lymphoplasmacytic Lymphoma 47 0.021
929
P ENC008 Encephalocele 47 0.021
930
ZKF001 Zika Fever 47 0.021
931
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.021
932
c CNG216 Congenital Hydrocephalus 47 0.021
933
P KRN004 Kernicterus 47 0.021
934
P THP004 Thiopurines, Poor Metabolism of, 1 47 0.021
935
PLS025 Plasmablastic Lymphoma 47 0.021
936
CNT033 Central Nervous System Cancer 47 0.021
937
c CRG004 Crigler-Najjar Syndrome, Type Ii 47 0.021
938
CRD137 Cardiogenic Shock 47 0.021
939
CHR074 Choriocarcinoma 47 0.021
940
NSS002 Neisseria Meningitidis Infection 47 0.021
941
RYN005 Raynaud Phenomenon 47 0.021
942
MYC005 Myocardial Stunning 46 0.021
943
MNN020 Meningococcal Infection 46 0.021
944
PLL012 Pollen Allergy 46 0.021
945
P BRB001 Beriberi 46 0.021
946
PLY012 Polyhydramnios 46 0.021
947
MGC001 Megacolon 46 0.021
948
P BNG032 Benign Mesothelioma 46 0.021
949
ANP006 Anaplastic Ependymoma 46 0.021
950
RCT017 Rectal Disease 46 0.021
951
SBP004 Subependymoma 46 0.021
952
MYX001 Myxopapillary Ependymoma 46 0.021
953
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.021
954
c DRR009 Diarrhea 6 46 0.021
955
ANR004 Anuria 46 0.021
956
c ACT042 Acute Pyelonephritis 46 0.021
957
P HRN001 Horner's Syndrome 45 0.021
958
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.021
959
MXD026 Mixed Glioma 45 0.021
960
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.021
961
INT253 Intestinal Benign Neoplasm 45 0.021
962
PLR022 Pleural Disease 45 0.021
963
c CRN278 Craniosynostosis 1 45 0.021
964
HMR002 Hemarthrosis 45 0.021
965
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.021
966
LYM051 Lymphomatoid Granulomatosis 45 0.021
967
c ACQ014 Acquired Hemophilia 45 0.021
968
CNT017 Central Nervous System Origin Vertigo 45 0.021
969
ASP008 Aspiration Pneumonitis 45 0.021
970
SPS057 Spasticity 45 0.021
971
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.021
972
DNB001 Danubian Endemic Familial Nephropathy 44 0.021
973
GRN017 Granulocytopenia 44 0.021
974
LTH001 Lethal Midline Granuloma 44 0.021
975
c PCH010 Pachyonychia Congenita 3 44 0.021
976
IRT001 Iritis 44 0.021
977
P PRL003 Proliferative Glomerulonephritis 44 0.021
978
GNG003 Gingival Recession 44 0.021
979
HPT067 Hepatocellular Adenoma 44 0.021
980
ISC015 Ischemic Colitis 44 0.021
981
c HYP272 Hypercholesterolemia, Familial, 3 44 0.021
982
P BCT020 Bacteremia 2 44 0.021
983
P EPN001 Ependymoblastoma 44 0.021
984
EMP001 Empty Sella Syndrome 44 0.021
985
c ADL023 Adult Medulloblastoma 44 0.021
986
URT014 Ureterolithiasis 44 0.021
987
ANP009 Anaplastic Oligodendroglioma 43 0.021
988
SPN369 Spinal Disease 43 0.021
989
AND001 Anodontia 43 0.021
990
P TST026 Testicular Germ Cell Cancer 43 0.021
991
BNM001 Bone Marrow Cancer 43 0.021
992
CRS001 Crescentic Glomerulonephritis 43 0.021
993
TRN021 Transaldolase Deficiency 43 0.021
994
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.021
995
P PRP034 Purpura Fulminans 43 0.021
996
P MJR007 Major Affective Disorder 1 43 0.021
997
MCR103 Microtia 43 0.021
998
BNS003 Binswanger's Disease 42 0.021
999
P AVS003 Avascular Necrosis 42 0.021
1000
c RTN047 Retinitis Pigmentosa 18 42 0.021
1001
P CLS010 Cluster Headache 42 0.021
1002
CHR286 Chronic Neutrophilic Leukemia 42 0.021
1003
c MLG079 Malignant Pleural Mesothelioma 42 0.021
1004
IDP091 Idiopathic Nephrotic Syndrome 42 0.021
1005
ADN020 Adenosarcoma 42 0.021
1006
c PST022 Posterior Uveal Melanoma 42 0.021
1007
ANC002 Anca-Associated Vasculitis 41 0.021
1008
c MLG064 Malignant Ependymoma 41 0.021
1009
EPC002 Epicondylitis 41 0.021
1010
BKS003 Beukes Hip Dysplasia 41 0.021
1011
PRM013 Premature Menopause 41 0.021
1012
c FBR072 Febrile Seizures, Familial, 11 41 0.021
1013
c RTN090 Retinitis Pigmentosa 55 41 0.021
1014
P HYP009 Hypertrophic Pyloric Stenosis 41 0.021
1015
NNT008 Neonatal Abstinence Syndrome 41 0.021
1016
PST053 Postherpetic Neuralgia 40 0.021
1017
P MLG074 Malignant Mesenchymoma 40 0.021
1018
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.021
1019
ANX004 Anoxia 40 0.021
1020
PSR016 Psoriatic Juvenile Idiopathic Arthritis 40 0.021
1021
ADJ001 Adjustment Disorder 40 0.021
1022
CLP006 Clopidogrel Resistance 40 0.021
1023
MLT001 Multiple Chemical Sensitivity 40 0.021
1024
UTR043 Uterine Sarcoma 39 0.021
1025
C1N001 C1 Inhibitor Deficiency 39 0.021
1026
EXT006 Extrahepatic Cholestasis 39 0.021
1027
PLC009 Placenta Praevia 39 0.021
1028
SCR015 Scarlet Fever 39 0.021
1029
ALG001 Algoneurodystrophy 39 0.021
1030
SPP007 Suppression Amblyopia 39 0.021
1031
HYP344 Hyperthyroidism, Familial Gestational 39 0.021
1032
c PLM022 Pulmonary Valve Insufficiency 39 0.021
1033
FML031 Female Stress Incontinence 39 0.021
1034
NTR042 Neutrophilic Dermatosis, Acute Febrile 38 0.021
1035
c OVR114 Ovarian Cancer 1 38 0.021
1036
PRP005 Parapsoriasis 38 0.021
1037
OPT010 Optic Papillitis 38 0.021
1038
ORN001 Ornithosis 38 0.021
1039
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.021
1040
c AML017 Amelogenesis Imperfecta, Type Ib 37 0.021
1041
CRB026 Cerebellar Astrocytoma 37 0.021
1042
CRN088 Craniorachischisis 37 0.021
1043
ATM052 Autoimmune Disease 1 37 0.021
1044
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.021
1045
SYS071 Systemic Autoimmune Disease 37 0.021
1046
P DNT007 Dentin Sensitivity 36 0.021
1047
c HRS036 Hirschsprung Disease 2 36 0.021
1048
HRW001 Hair Whorl 36 0.021
1049
PLC002 Plica Syndrome 36 0.021
1050
RHM036 Rheumatoid Arthritis Interstitial Lung Disease 36 0.021
1051
EPD005 Epidural Abscess 35 0.021
1052
OLG006 Oligoastrocytoma 35 0.021
1053
ANS004 Anisometropia 35 0.021
1054
P PRG002 Progesterone-Receptor Positive Breast Cancer 35 0.021
1055
CHR178 Chromosomal Triplication 35 0.021
1056
END072 Endotheliitis 35 0.021
1057
OPT032 Optic Pathway Glioma 35 0.021
1058
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.021
1059
c MJR008 Major Affective Disorder 2 35 0.021
1060
ATX010 Ataxia Neuropathy Spectrum 34 0.021
1061
c LKM005 Leukemia, T-Cell, Chronic 34 0.021
1062
GRM010 Germ Cells Tumors 34 0.021
1063
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.021
1064
c ADL008 Adult Oligodendroglioma 34 0.021
1065
ISL062 Isolated Plagiocephaly 34 0.021
1066
c RST012 Restless Legs Syndrome 1 34 0.021
1067
SML014 Small Intestine Leiomyosarcoma 34 0.021
1068
c MJR023 Major Affective Disorder 7 33 0.021
1069
PPL052 Papillomatosis, Confluent and Reticulated 33 0.021
1070
BNN005 Bunion 33 0.021
1071
RFR002 Refractory Hairy Cell Leukemia 33 0.021
1072
ACT064 Acute Necrotizing Encephalitis 33 0.021
1073
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.021
1074
c MJR003 Major Affective Disorder 6 33 0.021
1075
c MJR006 Major Affective Disorder 5 33 0.021
1076
TXC020 Toxic Oil Syndrome 33 0.021
1077
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.021
1078
CHL057 Childhood Brain Stem Glioma 32 0.021
1079