Search results for Propyl alcohol

769 hits were found for Propyl alcohol

# Family MCID Name MIFTS Score
1
ALC007 Alcohol Dependence 65 139.950
2
NNL005 Non-Alcoholic Fatty Liver Disease 63 77.829
3
FTT001 Fatty Liver Disease 61 65.102
4
NNL006 Non-Alcoholic Steatohepatitis 54 56.246
5
P LVR013 Liver Disease 68 46.426
6
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 31.873
7
LVR012 Liver Cirrhosis 62 25.740
8
CHL131 Chlorpropamide-Alcohol Flushing 21 25.261
9
P SBS003 Substance Abuse 54 24.811
10
WRN002 Wernicke-Korsakoff Syndrome 49 18.871
11
P HPT021 Hepatitis 68 18.777
12
WTH001 Withdrawal Disorder 47 18.600
13
P PNC044 Pancreatitis 61 17.876
14
ANX010 Anxiety 70 14.620
15
DPR016 Depression 64 14.459
16
MNT002 Mental Depression 56 14.038
17
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 13.784
18
c ACT027 Acute Pancreatitis 60 13.548
19
SJG002 Sjogren-Larsson Syndrome 53 13.114
20
c TYP009 Type 2 Diabetes Mellitus 91 12.817
21
c HPT001 Hepatitis C 61 12.649
22
DRG003 Drug Dependence 46 12.505
23
c HPT003 Hepatitis a 63 12.498
24
c ATR087 Atrial Standstill 1 74 12.107
25
P BPL003 Bipolar Disorder 56 11.832
26
TBC004 Tobacco Addiction 63 11.738
27
c MJR022 Major Affective Disorder 8 37 11.727
28
c MJR024 Major Affective Disorder 9 40 11.727
29
P HPT023 Hepatocellular Carcinoma 95 11.434
30
P TRM003 Tremor 50 11.352
31
P CRN300 Coronary Heart Disease 1 73 11.352
32
P MJR001 Major Depressive Disorder 68 11.258
33
c VRL010 Viral Hepatitis 52 11.158
34
P ENC018 Encephalopathy 62 11.125
35
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 11.054
36
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 11.039
37
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 11.039
38
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 11.039
39
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 11.039
40
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 11.039
41
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 11.039
42
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 11.039
43
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 11.039
44
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 11.039
45
PSY004 Psychotic Disorder 66 10.858
46
c HPT073 Hepatitis C Virus 70 10.685
47
P SMK004 Smoking As a Quantitative Trait Locus 3 44 10.619
48
LPD008 Lipid Metabolism Disorder 61 10.531
49
P SZR006 Seizure Disorder 69 10.424
50
P ATT013 Attention Deficit-Hyperactivity Disorder 65 10.354
51
MDD011 Mood Disorder 61 10.107
52
P DBT009 Diabetes Mellitus 67 10.017
53
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 9.997
54
TRM010 Traumatic Brain Injury 50 9.855
55
HMN044 Human Immunodeficiency Virus Type 1 76 9.651
56
IMM167 Immune Deficiency Disease 76 9.469
57
ESP021 Esophageal Cancer 84 9.392
58
P BRB001 Beriberi 44 9.320
59
P NRP001 Neuropathy 59 9.319
60
P HYP750 Hypertriglyceridemia, Familial 61 9.308
61
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 9.249
62
BRN071 Brain Injury 50 9.041
63
ORL011 Oral Cancer 60 8.794
64
WRN003 Wernicke Encephalopathy 45 8.792
65
P MYP004 Myopathy 67 8.775
66
HYP056 Hypoglycemia 65 8.489
67
OCL069 Ocular Motor Apraxia 57 8.309
68
ACQ007 Acquired Immunodeficiency Syndrome 58 8.282
69
HPT004 Hepatic Coma 43 8.275
70
VRC005 Varicose Veins 59 8.173
71
47X002 47,xyy 47 8.108
72
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 8.104
73
CHL068 Cholestasis 61 8.061
74
P PNC035 Pancreatic Cancer 87 8.036
75
48X005 48,xyyy 39 7.945
76
CCN001 Cocaine Dependence 47 7.938
77
P BRS047 Breast Cancer 97 7.895
78
AGN016 Aging 53 7.882
79
CCN002 Cocaine Abuse 49 7.840
80
HMN014 Human Immunodeficiency Virus Infectious Disease 54 7.782
81
AMN003 Amnestic Disorder 53 7.758
82
P PRP019 Peripheral Nervous System Disease 57 7.728
83
P HRT032 Heart Disease 84 7.568
84
P HYP086 Hypothyroidism 68 7.414
85
HDN002 Head Injury 44 7.398
86
SVR004 Severe Combined Immunodeficiency 70 7.370
87
HYP066 Hyperglycemia 60 7.352
88
P GST044 Gastritis 55 7.340
89
c HYP836 Hypercholesterolemia, Familial, 1 73 7.290
90
OPT003 Opiate Dependence 49 7.246
91
P SCH015 Schizophrenia 74 7.185
92
HMS001 Hemosiderosis 48 7.178
93
P CHR345 Chronic Pain 50 7.168
94
P RRH023 Rare Hereditary Hemochromatosis 52 7.099
95
P PLY019 Polyneuropathy 52 7.075
96
CNT047 Contact Dermatitis 56 7.039
97
PST011 Pustulosis of Palm and Sole 52 6.919
98
P PSR002 Psoriasis 63 6.862
99
c CHR684 Chronic Kidney Disease 73 6.722
100
P PRD008 Periodontitis 63 6.617
101
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 6.604
102
c DLT002 Dilated Cardiomyopathy 79 6.579
103
GLC003 Glucose Intolerance 53 6.576
104
CYT002 Cytokine Deficiency 43 6.541
105
P SLP005 Sleep Disorder 61 6.537
106
c HPT016 Hepatitis B 62 6.510
107
P KDN018 Kidney Disease 71 6.469
108
IMP005 Impotence 52 6.466
109
SQM006 Squamous Cell Carcinoma 59 6.415
110
GT001 Gout 63 6.406
111
ALL029 Allergic Disease 61 6.343
112
c HYP595 Hypertension, Essential 84 6.329
113
P MYP006 Myopia 55 6.326
114
PLM001 Pulmonary Tuberculosis 69 6.287
115
ANG054 Angina Pectoris 65 6.283
116
P VSC007 Vascular Disease 62 6.247
117
ISC004 Ischemia 61 6.233
118
END040 Endogenous Depression 54 6.091
119
KRT002 Keratomalacia 54 6.082
120
P DMN002 Dementia 65 6.030
121
P PRP029 Porphyria 60 6.019
122
PRT036 Peritonitis 65 5.943
123
ADN018 Adenoma 58 5.929
124
DWN001 Down Syndrome 70 5.914
125
MTB004 Metabolic Acidosis 48 5.886
126
DRM006 Dermatitis 61 5.855
127
PTH002 Pathological Gambling 48 5.815
128
P SLP006 Sleep Apnea 69 5.754
129
ALL010 Allergic Contact Dermatitis 55 5.739
130
CRD132 Cardiac Conduction Defect 59 5.710
131
P MYC084 Mycobacterium Tuberculosis 1 68 5.698
132
SKN016 Skin Disease 63 5.694
133
HYP060 Hyperinsulinism 53 5.676
134
HYP014 Hyperuricemia 51 5.621
135
LPP008 Lipoprotein Quantitative Trait Locus 65 5.617
136
BLM002 Bulimia Nervosa 56 5.594
137
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 5.542
138
IRN002 Iron Metabolism Disease 56 5.524
139
P HDC001 Headache 56 5.516
140
P HYP076 Hyperthyroidism 53 5.512
141
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 5.460
142
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 5.410
143
ART140 Arteries, Anomalies of 52 5.340
144
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 5.328
145
P HRP006 Herpes Simplex 65 5.323
146
CRB039 Cerebrovascular Disease 65 5.255
147
PRS021 Prostatic Adenoma 43 5.246
148
RPD005 Rapidly Involuting Congenital Hemangioma 48 5.197
149
HRW001 Hair Whorl 35 5.193
150
P GST053 Gastric Cancer 82 5.185
151
PRS129 Prostatic Hyperplasia, Benign 48 5.180
152
RCK004 Rickets 64 5.178
153
CNG034 Congestive Heart Failure 69 5.142
154
P ATR011 Atrial Fibrillation 66 5.133
155
P PNM007 Pneumonia 64 5.127
156
HYP266 Hypoxia 56 5.099
157
c ACT071 Acute Kidney Failure 60 5.092
158
c MGR028 Migraine with or Without Aura 1 63 5.077
159
P ALZ034 Alzheimer Disease 87 5.055
160
P TRN020 Turner Syndrome 67 5.040
161
P RHM011 Rheumatoid Arthritis 81 5.030
162
P NRB001 Neuroblastoma 66 5.013
163
P DDN001 Duodenal Ulcer 52 5.004
164
P EPL164 Epilepsy 70 5.001
165
P RSP003 Respiratory Failure 73 4.988
166
ALL003 Allergic Rhinitis 66 4.954
167
DSS032 Disease by Infectious Agent 55 4.942
168
PTH003 Pathologic Nystagmus 52 4.940
169
P LNG032 Lung Cancer 98 4.927
170
PRS045 Prostatic Hypertrophy 53 4.926
171
P BND020 Bone Disease 60 4.905
172
GST023 Gastric Ulcer 52 4.896
173
c GLL024 Gallbladder Disease 1 53 4.862
174
SXL003 Sexual Disorder 49 4.828
175
P RHN004 Rhinitis 56 4.809
176
BCT022 Bacterial Infectious Disease 55 4.786
177
STR067 Stroke, Ischemic 79 4.777
178
P INF032 Infertility 60 4.759
179
P DRR001 Diarrhea 55 4.736
180
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 4.722
181
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 4.722
182
P ADN016 Adenocarcinoma 63 4.719
183
P MYC007 Myocardial Infarction 69 4.714
184
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 4.714
185
P OST002 Osteoporosis 76 4.694
186
P AST005 Asthma 75 4.602
187
DFC004 Deficiency Anemia 74 4.590
188
P ART022 Arthritis 70 4.568
189
c DNT047 Dentinogenesis Imperfecta Type 2 35 4.530
190
PLM129 Pulmonary Disease, Chronic Obstructive 74 4.474
191
P PRK039 Parkinsonism 55 4.441
192
BNR002 Bone Resorption Disease 47 4.429
193
P PRS040 Prostate Cancer 95 4.428
194
NRL016 Neural Tube Defects 80 4.413
195
GNG013 Gingivitis 59 4.400
196
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 4.390
197
SPP007 Suppression Amblyopia 38 4.371
198
AMB002 Amblyopia 49 4.371
199
P LCT001 Lactic Acidosis 50 4.360
200
PNC129 Pancreatic Adenocarcinoma 64 4.354
201
GST033 Gestational Diabetes 60 4.353
202
P LYM118 Lymphoma 66 4.345
203
c ACT075 Acute Myocardial Infarction 55 4.335
204
HLX001 Helix Syndrome 47 4.272
205
P SYP003 Syphilis 59 4.266
206
P THR014 Thrombocytopenia 66 4.264
207
ATN005 Autonomic Dysfunction 45 4.263
208
GLB002 Glioblastoma 67 4.221
209
P LRY044 Larynx Cancer 53 4.220
210
ANR007 Anorexia Nervosa 59 4.207
211
GST050 Gastrointestinal System Disease 55 4.189
212
P EXN002 Exanthem 58 4.177
213
P BLD134 Bladder Cancer 79 4.156
214
GLM045 Glioma 62 4.127
215
GLL048 Glial Tumor 51 4.121
216
P ART021 Arteriosclerosis 53 4.109
217
P GLM007 Glomerulonephritis 59 4.028
218
SVR001 Severe Acute Respiratory Syndrome 68 4.020
219
P CND004 Candidiasis 57 4.009
220
CRD223 Cardiac Arrhythmia 63 4.006
221
P INF037 Inflammatory Bowel Disease 53 3.983
222
c MCR120 Microvascular Complications of Diabetes 7 47 3.980
223
PRP027 Peripheral Vascular Disease 71 3.971
224
KRT009 Keratosis 52 3.954
225
P MYC033 Myoclonus 46 3.931
226
PNG002 Pain Agnosia 51 3.894
227
SPN186 Spinal Cord Injury 60 3.889
228
MSC007 Muscle Hypertrophy 64 3.875
229
P ESP024 Esophagitis 60 3.875
230
CLT003 Colitis 63 3.864
231
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 3.864
232
PPL022 Papilloma 53 3.861
233
INS024 Insulin-Like Growth Factor I 77 3.849
234
END057 Endometrial Cancer 76 3.817
235
BRN024 Bronchitis 67 3.785
236
CRB004 Cerebral Artery Occlusion 45 3.772
237
c TYP008 Type 1 Diabetes Mellitus 77 3.771
238
END086 End Stage Renal Disease 54 3.769
239
P CRD246 Cardiovascular System Disease 55 3.758
240
HND015 Hand Skill, Relative 29 3.754
241
SQM002 Squamous Cell Papilloma 45 3.743
242
TXC005 Toxic Shock Syndrome 61 3.727
243
P CRD119 Cardiac Arrest 68 3.726
244
PLM010 Pulmonary Edema 54 3.715
245
THR024 Thrombosis 56 3.706
246
P NTR004 Neutropenia 62 3.693
247
VCC001 Vaccinia 49 3.689
248
STT001 Status Epilepticus 58 3.688
249
DYS073 Dysphagia 53 3.666
250
OST011 Osteomalacia 52 3.648
251
CHL123 Chlamydia 58 3.634
252
P GLM040 Glioma Susceptibility 1 70 3.633
253
P PLY011 Polycystic Ovary Syndrome 57 3.622
254
PRT251 Proteinuria, Chronic Benign 58 3.620
255
IRR002 Irritable Bowel Syndrome 64 3.584
256
P DYS154 Dystonia 64 3.579
257
PRP030 Purpura 54 3.570
258
P PTS002 Ptosis 52 3.566
259
c MCR115 Microvascular Complications of Diabetes 5 65 3.562
260
PRT058 Pure Autonomic Failure 58 3.557
261
HYP017 Hypophosphatemia 49 3.554
262
MLD018 Mild Cognitive Impairment 48 3.529
263
c MCR130 Microvascular Complications of Diabetes 6 41 3.510
264
c MCR133 Microvascular Complications of Diabetes 4 41 3.507
265
c MCR113 Microvascular Complications of Diabetes 3 52 3.507
266
P HML002 Hemolytic Anemia 62 3.497
267
CLF027 Cleft Palate, Isolated 64 3.459
268
P CTR002 Cataract 59 3.448
269
P DRM053 Dermatitis, Atopic 65 3.428
270
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 3.425
271
c ESS001 Essential Tremor 56 3.416
272
LYM133 Lymphoma, Hodgkin, Classic 69 3.410
273
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.403
274
SPS057 Spasticity 43 3.401
275
SDD001 Sudden Infant Death Syndrome 60 3.379
276
P OVR042 Ovarian Cancer 88 3.365
277
HPT022 Hepatoblastoma 54 3.362
278
SPL018 Splenomegaly 47 3.352
279
DNT012 Dental Caries 53 3.346
280
P URN019 Urinary Tract Infection 48 3.342
281
P SKN015 Skin Carcinoma 71 3.339
282
c ATS007 Autism Spectrum Disorder 71 3.327
283
ART016 Aortic Aneurysm 68 3.312
284
ANX004 Anoxia 40 3.290
285
P BCL017 B-Cell Lymphoma 57 3.284
286
c PLM127 Pulmonary Hypertension, Primary, 3 34 3.263
287
P MVM001 Movement Disease 61 3.263
288
P PRK057 Parkinson Disease, Late-Onset 79 3.257
289
P HNT016 Huntington Disease 73 3.254
290
ANR040 Aneurysm 60 3.244
291
P ANP001 Anaplastic Large Cell Lymphoma 59 3.228
292
ULC004 Ulcerative Colitis 74 3.223
293
P MSC003 Muscular Atrophy 52 3.217
294
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 3.209
295
SCH014 Schistosomiasis 56 3.209
296
P ACN011 Acne 55 3.203
297
CRB037 Cerebral Palsy 66 3.192
298
VTM002 Vitamin B12 Deficiency 48 3.169
299
P HYP069 Hyperparathyroidism 62 3.167
300
P HYP098 Hypereosinophilic Syndrome 66 3.143
301
HYP020 Hyperprolactinemia 63 3.124
302
LSH001 Leishmaniasis 63 3.112
303
P LTR001 Lateral Sclerosis 57 3.105
304
c AMY091 Amyotrophic Lateral Sclerosis 1 87 3.102
305
P NSP012 Nasopharyngeal Carcinoma 60 3.101
306
PST092 Posttransplant Acute Limbic Encephalitis 29 3.100
307
ATR057 Atrioventricular Block 54 3.095
308
P CLC063 Celiac Disease 1 65 3.090
309
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.082
310
c THR092 Thrombophilia Due to Thrombin Defect 74 3.072
311
OVR063 Overnutrition 42 3.060
312
TTN003 Tetanus 64 3.040
313
FBR047 Fibromyalgia 57 3.003
314
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.988
315
BRN004 Brain Edema 54 2.980
316
MYL069 Myeloma, Multiple 76 2.973
317
P ART023 Arthropathy 59 2.968
318
PRT037 Pertussis 49 2.963
319
CHG001 Chagas Disease 65 2.950
321
HGH043 High Grade Glioma 46 2.920
322
P KLZ004 Kala-Azar 1 41 2.915
323
LYM143 Lymphoma, Non-Hodgkin, Familial 74 2.910
324
P END044 Endometriosis 62 2.898
325
CRB011 Cerebrotendinous Xanthomatosis 64 2.891
326
BCK006 Back Pain 43 2.888
327
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 2.862
328
c LKM061 Leukemia, Acute Myeloid 83 2.861
329
P MYC008 Myocarditis 59 2.860
330
P LKM002 Leukemia 65 2.838
331
c HPT007 Hepatitis E 50 2.830
332
CHR100 Chronic Ulcer of Skin 57 2.826
333
PPL052 Papillomatosis, Confluent and Reticulated 34 2.820
334
ATM095 Autoimmune Disease 61 2.789
335
P LPR021 Leprosy 3 71 2.775
336
c GRV008 Graves Disease 1 54 2.774
337
LYM019 Lymphosarcoma 46 2.761
338
TRN015 Transient Cerebral Ischemia 62 2.754
339
P FBR017 Fibrosarcoma 55 2.747
340
INT007 Intermediate Coronary Syndrome 53 2.744
341
P URT039 Urticaria 57 2.738
342
P MLN007 Male Infertility 56 2.729
343
HNS001 Hansen's Disease 32 2.708
344
DMP001 Dumping Syndrome 43 2.698
345
SPN035 Spindle Cell Sarcoma 51 2.691
346
SRC014 Sarcoma 64 2.686
347
CYS001 Cystic Fibrosis 77 2.683
348
CMM005 Common Cold 55 2.682
349
MLG169 Malignant Astrocytoma 57 2.678
350
INT323 Intraocular Pressure Quantitative Trait Locus 63 2.672
351
CHC001 Chickenpox 56 2.645
352
c PRC016 Pre-Eclampsia 64 2.642
353
PLR008 Pleurisy 49 2.639
354
FML037 Female Breast Cancer 51 2.639
355
P ENC004 Encephalitis 61 2.632
356
P NRC002 Narcolepsy 55 2.609
357
URM002 Uremia 47 2.596
358
XNT003 Xanthomatosis 48 2.596
359
HYP026 Hypoglycemic Coma 37 2.591
360
GTR002 Goiter 52 2.590
361
LMY002 Leiomyoma 51 2.585
362
THY029 Thyroid Carcinoma 55 2.575
363
c BRN108 Branchiootic Syndrome 1 63 2.563
364
P GRV001 Graves' Disease 54 2.560
365
DYS015 Dysentery 49 2.529
366
P LNG064 Lung Cancer Susceptibility 3 69 2.529
367
OST159 Osteogenic Sarcoma 66 2.524
368
P PHC003 Pheochromocytoma 70 2.521
369
KPS004 Kaposi Sarcoma 76 2.512
370
GRN017 Granulocytopenia 42 2.467
371
P CNJ013 Conjunctivitis 66 2.456
372
IRN001 Iron Deficiency Anemia 58 2.450
373
CRV035 Cervical Cancer 72 2.439
374
P EYD002 Eye Disease 57 2.436
375
P INF038 Influenza 68 2.427
376
P BRS044 Breast Adenocarcinoma 58 2.424
377
MLN003 Melancholia 41 2.415
378
P VSC011 Vasculitis 61 2.406
379
CHL014 Cholera 62 2.393
380
P ASP006 Aspergillosis 71 2.374
381
P SRC025 Sarcoidosis 1 70 2.373
382
KRT019 Keratitis, Hereditary 66 2.365
383
PTT037 Pituitary Tumors 44 2.359
384
CRN030 Coronary Stenosis 50 2.354
385
P CMP008 Compartment Syndrome 49 2.335
386
GST045 Gastroenteritis 58 2.331
387
MYL009 Myelodysplastic Syndrome 67 2.324
388
DPH001 Diphtheria 59 2.314
389
P MCR129 Microvascular Complications of Diabetes 1 67 2.313
390
DBT010 Diabetic Neuropathy 54 2.311
391
KLB003 Klebsiella Pneumonia 49 2.303
392
c PCH010 Pachyonychia Congenita 3 43 2.297
393
CHR178 Chromosomal Triplication 33 2.296
394
HMN047 Human Cytomegalovirus Infection 59 2.286
395
SPN051 Spondylitis 51 2.270
396
HRT012 Heart Valve Disease 53 2.261
397
P KDN017 Kidney Cancer 60 2.261
398
PLY150 Polykaryocytosis Inducer 29 2.261
399
P LKM062 Leukemia, Acute Lymphoblastic 69 2.249
400
ADR040 Adrenal Gland Pheochromocytoma 45 2.241
401
P END047 Endophthalmitis 53 2.224
402
P EPL198 Epilepsy, Myoclonic Juvenile 61 2.218
403
PLL012 Pollen Allergy 44 2.213
404
CRY035 Cryptorchidism, Unilateral or Bilateral 57 2.191
405
VRL011 Viral Infectious Disease 60 2.184
406
P MYL006 Myeloid Leukemia 60 2.173
407
GST009 Gastroschisis 53 2.166
408
EXN003 Exencephaly 30 2.156
409
P SBR004 Seborrheic Dermatitis 44 2.155
410
c LKM063 Leukemia, Chronic Myeloid 70 2.153
411
P CLS010 Cluster Headache 42 2.138
412
PRM003 Premature Ejaculation 44 2.120
413
RST023 Resting Heart Rate, Variation in 40 2.114
414
P MYT002 Myotonic Dystrophy 51 2.109
415
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.101
416
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.096
417
P INS002 in Situ Carcinoma 52 2.088
418
TLN003 Telangiectasis 51 2.076
419
P GLL020 Gallbladder Disease 57 2.073
420
FSC004 Fasciitis 49 2.067
421
RTR001 Retrograde Amnesia 41 2.057
422
P PLM037 Pulmonary Hypertension 69 2.057
423
CWP001 Cowpox 44 2.056
424
ADG002 Audiogenic Seizures 25 2.031
425
NRR001 Neuroretinitis 42 2.021
426
RTN023 Retinitis 45 2.021
427
ORL004 Oral Submucous Fibrosis 56 2.016
428
MCS002 Mucositis 55 2.012
429
TRD006 Tardive Dyskinesia 53 1.995
430
c SML038 Small Cell Cancer of the Lung 68 1.988
431
SFT003 Soft Tissue Sarcoma 43 1.978
432
MLR004 Malaria 77 1.978
433
STM007 Stomatitis 52 1.972
434
P THL005 Thalassemia 56 1.963
435
DWR001 Dwarfism 44 1.963
436
ORL005 Oral Candidiasis 55 1.958
437
MCL006 Macular Retinal Edema 56 1.945
438
BRN002 Bronchiolitis 57 1.932
439
NCR007 Necrotizing Fasciitis 48 1.921
440
P GRF003 Graft-Versus-Host Disease 71 1.916
441
P BNG032 Benign Mesothelioma 53 1.912
442
P NPH012 Nephrotic Syndrome 61 1.912
443
GST040 Gastric Adenocarcinoma 66 1.906
444
TRC003 Trichomoniasis 53 1.894
445
INS001 Insulinoma 59 1.875
446
ANV001 Anovulation 46 1.875
447
ACT098 Acute Erythroid Leukemia 55 1.872
448
ARG004 Argyria 26 1.867
449
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.865
450
AST006 Astigmatism 46 1.862
451
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.839
452
c LKM005 Leukemia, T-Cell, Chronic 33 1.839
453
CND006 Candida Glabrata 29 1.836
454
P LKM071 Leukemia, Chronic Lymphocytic 74 1.835
455
FNG017 Fungal Infectious Disease 54 1.821
456
PLC005 Placental Insufficiency 55 1.813
457
AMP007 Amphetamine Abuse 36 1.810
458
MTH071 Methane Production 24 1.807
459
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 1.797
460
HRP004 Herpes Zoster 60 1.795
461
P APL001 Aplastic Anemia 72 1.792
463
c ACT073 Acute Leukemia 59 1.781
464
PRS063 Paresthesia 39 1.780
465
P PTT006 Pituitary Adenoma 55 1.780
466
GNG011 Gingival Disease 53 1.764
467
P TBR001 Tuberous Sclerosis 69 1.746
468
c MCR112 Microvascular Complications of Diabetes 2 42 1.744
469
c SCN007 Secondary Hyperparathyroidism 50 1.734
470
P RTN024 Retinoblastoma 72 1.727
471
RTN020 Retinal Vascular Disease 45 1.698
472
MNN032 Meningococcal Meningitis 52 1.694
473
HMP009 Haemophilus Influenzae 41 1.680
474
ALL014 Allergic Encephalomyelitis 34 1.669
475
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 1.668
476
CRB090 Cerebral Hypoxia 42 1.668
477
P PRN023 Prion Disease 60 1.665
478
SML019 Smallpox 55 1.663
479
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.663
480
CHR073 Choreatic Disease 53 1.663
481
FCL014 Focal Epilepsy 53 1.659
482
NRL004 Neuroleptic Malignant Syndrome 52 1.657
483
INF009 Inflammatory Spondylopathy 30 1.656
484
NRN004 Neuroendocrine Tumor 55 1.646
485
P KRT007 Keratoconus 49 1.629
486
SPS019 Spastic Paraparesis 38 1.625
487
SYN007 Synovitis 54 1.622
488
IGR001 Ige Responsiveness, Atopic 58 1.617
489
MSL001 Measles 61 1.611
490
P MSC005 Muscular Dystrophy 66 1.608
491
P FRG001 Fragile X Syndrome 70 1.606
492
CHL056 Cheilitis 46 1.597
493
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 1.595
494
P TXP001 Toxoplasmosis 59 1.593
495
CRY005 Cryptococcosis 61 1.590
496
TRY001 Trypanosomiasis 50 1.586
497
PHN003 Phenylketonuria 76 1.583
498
MLT157 Multiple System Atrophy 1 69 1.580
499
c CNG006 Congenital Hypothyroidism 63 1.551
500
P MNC007 Monocytic Leukemia 48 1.541
501
c MCR312 Microphthalmia, Syndromic 10 39 1.538
502
ART006 Arthus Reaction 40 1.532
503
ALL006 Allergic Asthma 55 1.529
504
CNN005 Connective Tissue Disease 66 1.528
505
ABD010 Abdominal Wall Defect 37 1.528
506
LMB062 Limb Ischemia 55 1.527
507
AMB001 Amebiasis 56 1.524
508
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.521
509
MTN003 Motion Sickness 50 1.515
510
VLV011 Vulvovaginal Candidiasis 49 1.513
511
HYP025 Hyperphosphatemia 47 1.508
512
RYS001 Reye Syndrome 49 1.506
513
MYF001 Myofibroma 42 1.506
514
LYS012 Lysosomal Acid Lipase Deficiency 64 1.502
515
ATS010 Autosomal Recessive Disease 42 1.502
516
SRT004 Serotonin Syndrome 54 1.501
517
ERL001 Early Myoclonic Encephalopathy 62 1.489
518
P TMP001 Temporal Lobe Epilepsy 49 1.484
519
MYC019 Mycobacterium Marinum 29 1.481
520
CHR074 Choriocarcinoma 46 1.478
521
PLM031 Poliomyelitis 62 1.475
522
GST019 Gastrointestinal Stromal Tumor 78 1.470
523
PLG002 Plague 58 1.464
524
VSC003 Visceral Leishmaniasis 54 1.454
525
INT075 Intracranial Hypertension 52 1.451
526
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.436
527
P ATX030 Ataxia-Telangiectasia 80 1.430
528
MST004 Mast Cell Neoplasm 41 1.429
529
EXT007 Extracutaneous Mastocytoma 38 1.429
530
P OVR049 Ovarian Disease 50 1.428
531
CHL050 Cholesterol Ester Storage Disease 30 1.422
532
LWC001 Low Compliance Bladder 44 1.411
533
c PRG020 Paragangliomas 3 39 1.405
534
CHD004 Chudley-Mccullough Syndrome 47 1.400
535
EMB004 Embryonal Carcinoma 55 1.399
536
P RTT002 Rett Syndrome 79 1.397
537
MYT011 Myotonia 37 1.379
538
APH001 Aphthous Stomatitis 57 1.376
539
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.357
540
TST015 Testicular Disease 42 1.356
541
CLN015 Colon Adenocarcinoma 64 1.348
542
c THY107 Thymoma, Familial 42 1.343
543
P THY023 Thymoma 64 1.343
544
PHR003 Pharyngitis 57 1.340
545
CYS005 Cysticercosis 60 1.336
546
CCC002 Coccidiosis 50 1.333
547
BCT021 Bacterial Sepsis 43 1.330
548
PNM013 Pneumococcal Meningitis 43 1.328
549
BNN003 Bone Inflammation Disease 47 1.324
550
P FNG006 Feingold Syndrome 1 61 1.318
551
PLS007 Plasmodium Falciparum Malaria 52 1.311
552
P HMN032 Human Herpesvirus 8 47 1.305
553
CRY004 Cryoglobulinemia 47 1.301
554
THR016 Thrombophlebitis 50 1.297
555
P SML001 Small Cell Carcinoma 52 1.293
556
BNG077 Benign Idiopathic Neonatal Seizures 23 1.291
557
c BTT014 Beta-Thalassemia 72 1.289
558
PLC002 Plica Syndrome 35 1.283
559
P MTR014 Motor Neuron Disease 65 1.279
560
GRD001 Giardiasis 46 1.278
561
AVN001 Avian Influenza 61 1.277
562
LYM009 Lymphocytic Choriomeningitis 46 1.258
563
P DNG005 Dengue Virus 55 1.256
564
LGN002 Legionellosis 61 1.251
565
LGN006 Legionnaire Disease 52 1.246
566
c DWL002 Dowling-Degos Disease 1 58 1.233
567
P RTN008 Retinitis Pigmentosa 79 1.227
568
P THY032 Thyroiditis 56 1.217
569
RYN005 Raynaud Phenomenon 45 1.212
570
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.209
571
P RHB003 Rhabdomyosarcoma 66 1.209
572
NRS003 Neurosyphilis 45 1.208
573
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 1.205
574
MTH009 Mouth Disease 57 1.203
575
P MLG074 Malignant Mesenchymoma 40 1.189
576
P UVT001 Uveitis 57 1.188
577
ACR007 Acromegaly 70 1.187
578
AMN006 Aminoaciduria 37 1.182
579
c TBR025 Tuberous Sclerosis 1 84 1.179
580
HST011 Histoplasmosis 54 1.179
581
P ANT006 Antiphospholipid Syndrome 55 1.151
582
WLL004 Wallerian Degeneration 38 1.145
583
P TRT019 Torticollis 47 1.140
584
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.132
585
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.130
586
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.130
587
CLR109 Colorectal Adenocarcinoma 50 1.130
588
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.121
589
CYS009 Cystadenoma 42 1.108
590
P FBR031 Febrile Seizures 52 1.103
591
ASY002 Asymptomatic Neurosyphilis 41 1.095
592
WST005 West Nile Virus 55 1.090
593
MYC017 Mycobacterium Kansasii 36 1.085
594
MYS004 Myiasis 38 1.083
595
LNN001 Lennox-Gastaut Syndrome 61 1.081
596
P HYP040 Hypospadias 51 1.073
597
P PRT096 Peritoneal Mesothelioma 49 1.067
598
MDD018 Middle East Respiratory Syndrome 44 1.063
599
ADR016 Adrenal Cortical Carcinoma 61 1.054
600
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 1.051
601
c ALB021 Albinism, Oculocutaneous, Type Ii 58 1.051
602
P RPD001 Rapidly Progressive Glomerulonephritis 43 1.050
603
NPH010 Nephrosclerosis 50 1.034
604
P ZLL001 Zellweger Syndrome 65 1.030
605
P LNG028 Long Qt Syndrome 63 1.028
606
MSN001 Mesangial Proliferative Glomerulonephritis 44 1.015
607
CRV040 Cervix Carcinoma 50 1.015
608
PST010 Pasteurellosis 38 1.014
609
ASP030 Aspirin Resistance 41 1.009
610
SCK003 Sickle Cell Anemia 74 1.007
611
GNT003 Genital Herpes 54 1.001
612
PRT029 Parathyroid Adenoma 51 0.997
613
c CHR711 Chronic Asthma 41 0.994
614
ANP005 Anaplastic Astrocytoma 59 0.989
615
P RNV001 Renovascular Hypertension 48 0.987
616
P SPP010 Suppressor of Tumorigenicity 3 50 0.980
617
IRD001 Iridocyclitis 54 0.978
618
P LTH003 Lethal Congenital Contracture Syndrome 40 0.976
619
P BNC003 Bone Cancer 58 0.969
620
P CHN012 Chondrosarcoma 56 0.963
621
LST001 Listeriosis 59 0.961
622
P MTH007 Methemoglobinemia 46 0.956
623
ADR005 Adrenal Carcinoma 58 0.955
624
YLL002 Yellow Fever 61 0.952
625
P GCH001 Gaucher's Disease 69 0.950
626
PLY100 Polyploidy 36 0.949
627
ECT004 Ecthyma 26 0.944
628
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.942
629
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.934
630
BRK010 Burkitt Lymphoma 65 0.930
631
DMY004 Demyelinating Disease 50 0.929
632
ZLL002 Zollinger-Ellison Syndrome 55 0.920
633
CRC021 Carcinosarcoma 62 0.917
634
RTN017 Retinal Detachment 60 0.898
635
P AGM001 Agammaglobulinemia 67 0.894
636
MST020 Mast Cell Activation Syndrome 27 0.887
637
c RNG008 Ring Chromosome 13 31 0.886
638
NWC001 Newcastle Disease 47 0.883
639
SHG001 Shigellosis 61 0.882
640
TRN018 Transitional Cell Carcinoma 56 0.859
641
c BCT006 Bacterial Conjunctivitis 43 0.831
642
CRT015 Carotid Artery Occlusion 45 0.827
643
SPN221 Spina Bifida Occulta 39 0.821
644
ALV001 Alveolar Periostitis 34 0.821
645
RBS001 Rabies 57 0.820
646
THY030 Thyroid Gland Disease 50 0.816
647
CHK001 Chikungunya 60 0.814
648
c SCH079 Schizophrenia 1 44 0.810
649
ANT024 Anthrax Disease 57 0.810
650
JPN002 Japanese Encephalitis 61 0.808
651
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.806
652
MSC157 Muscular Dystrophy, Duchenne Type 78 0.801
653
PTN004 Patent Ductus Venosus 31 0.797
654
ALB002 Albinism 46 0.793
655
CYN003 Cyanide Poisoning 22 0.783
656
HRN029 Hearing Loss, Noise-Induced 37 0.779
657
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 0.778
658
P MPL001 Maple Syrup Urine Disease 69 0.776
659
ADN067 Adenoid Hypertrophy 38 0.773
660
c SCL052 Scleroderma, Familial Progressive 60 0.772
661
URT049 Urate Oxidase, Pseudogene 24 0.768
662
P VNS003 Venous Insufficiency 54 0.761
663
ENC010 Encephalocraniocutaneous Lipomatosis 46 0.760
664
MLT152 Multiple Self-Healing Squamous Epithelioma 44 0.760
665
c CHR417 Chronic Graft Versus Host Disease 55 0.751
666
ADN002 Adenoiditis 36 0.747
667
VRL003 Variola Major 43 0.747
668
PRS036 Parasitic Protozoa Infectious Disease 44 0.740
669
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.737
670
EXP004 Exophthalmos 50 0.733
671
TBL029 Tubulin, Beta 28 0.730
672
SPN187 Spinocerebellar Atrophy 23 0.729
673
P MDL005 Medulloblastoma 75 0.728
674
c VRL005 Viral Pneumonia 52 0.727
675
EPD015 Epidemic Typhus 44 0.720
676
c RNG024 Ring Chromosome 8 28 0.718
677
SLP001 Sleeping Sickness 56 0.717
678
SCR008 Scrub Typhus 57 0.713
679
CMB007 Combined Immunodeficiency 56 0.697
680
CRT004 Carotid Artery Thrombosis 39 0.692
681
P PRC019 Precocious Puberty 48 0.692
682
THR123 Thrombotic Microangiopathy 40 0.685
683
c SBC007 Subacute Thyroiditis 43 0.684
684
MRF001 Marfan Syndrome 76 0.672
685
CYT005 Cytomegalovirus Retinitis 50 0.670
686
URT010 Ureteral Obstruction 44 0.664
687
P CHR071 Charcot-Marie-Tooth Disease 64 0.662
688
BLD131 Bladder Urothelial Carcinoma 59 0.646
689
GRM010 Germ Cells Tumors 33 0.637
690
ACT228 Acute Radiation Syndrome 30 0.634
691
c CHR708 Chronic Urticaria 42 0.632
692
P RTN016 Retinal Degeneration 52 0.629
693
RTN021 Retinal Vascular Occlusion 45 0.620
694
SCR011 Scrapie 39 0.615
695
ACR008 Acrocallosal Syndrome 69 0.614
696
c RNG015 Ring Chromosome 2 22 0.610
697
CMP034 Complete Androgen Insensitivity Syndrome 55 0.609
698
MYC005 Myocardial Stunning 45 0.609
699
CRS001 Crescentic Glomerulonephritis 42 0.606
700
c ADL052 Adult Acute Lymphocytic Leukemia 46 0.600
701
DRV001 Dravet Syndrome 69 0.598
702
ANC002 Anca-Associated Vasculitis 44 0.597
703
PRX097 Paroxysmal Dystonia 32 0.597
704
THY128 Thyroid Tumor 33 0.582
705
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.575
706
THR113 Thiourea Tasting 19 0.552
707
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.552
708
PLY179 Polyomavirus-Associated Nephropathy 25 0.546
709
P PSD015 Pseudohypoparathyroidism 54 0.539
710
P LPS002 Liposarcoma 64 0.527
711
DRM009 Dermatomycosis 36 0.523
712
DBT006 Diabetic Macular Edema 48 0.514
713
P GNG009 Gangliosidosis 44 0.514
714
P CTN015 Cutaneous T Cell Lymphoma 48 0.503
715
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.500
716
MLG079 Malignant Pleural Mesothelioma 42 0.500
717
c CTR103 Cataract 4, Multiple Types 50 0.491
718
c 46X049 46,xy Sex Reversal 2 51 0.491
719
P PSD087 Pseudoxanthoma Elasticum 66 0.483
720
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.483
721
DYS011 Dyskinesia of Esophagus 41 0.483
722
OCL006 Ocular Hypertension 53 0.472
723
PRP001 Propionic Acidemia 65 0.464
724
HGH001 High Pressure Neurological Syndrome 28 0.464
725
DFF031 Diffuse Alveolar Hemorrhage 31 0.464
726
CYN002 Cyanosis, Transient Neonatal 43 0.459
727
GLY010 Glycine Encephalopathy 57 0.439
728
EPL131 Epilepsy, Pyridoxine-Dependent 46 0.439
729
ESN002 Eosinophilia-Myalgia Syndrome 40 0.439
730
AGM019 Agammaglobulinemia, X-Linked 71 0.377
731
ARM001 Aromatase Deficiency 54 0.377
732
LNG017 Lung Giant Cell Carcinoma 52 0.377
733
RFR013 Refractory Celiac Disease 33 0.377
734
TRT001 Teratocarcinoma 41 0.367
735
PPL002 Papillary Carcinoma 46 0.355
736
c RNG023 Ring Chromosome 7 43 0.328
737
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 39 0.317
738
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.315
739
P TMR010 Tumor Predisposition Syndrome 69 0.308
740
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.306
741
c EXD008 Exudative Vitreoretinopathy 1 71 0.297
742
P MMB011 Membranous Nephropathy 50 0.296
743
TXC020 Toxic Oil Syndrome 33 0.296
744
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.296
745
OCL010 Ocular Hypotension 37 0.283
746
MST021 Meester-Loeys Syndrome 37 0.265
747
BRT054 Brittle Bone Disorder 74 0.265
748
MCR088 Microscopic Polyangiitis 51 0.265
749
RTC009 Reticulum Cell Sarcoma 43 0.253
750
P SCL048 Sclerosteosis 58 0.240
751
HYP141 Hyperphenylalaninemia 42 0.240
752
RTC005 Reticulosarcoma 47 0.240
753
AML001 Amelanotic Melanoma 37 0.225
754
TRC023 Trichinosis 53 0.225
755
P LFR001 Li-Fraumeni Syndrome 73 0.209
756
VLK001 Volkmann Contracture 23 0.209
757
APN006 Apnea of Prematurity 24 0.190
758
THY122 Thyroid Gland Cancer 59 0.190
759
GLS001 Gliosarcoma 63 0.190
760
c GM1007 Gm1 Gangliosidosis 65 0.190
761
PRR015 Preauricular Fistulae, Congenital 20 0.164
762
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.164
763
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.164
764
PTT008 Pituitary Carcinoma 47 0.164
765
P CRV031 Cervical Adenocarcinoma 48 0.164
766
DFF012 Differentiating Neuroblastoma 27 0.164
767
OVR059 Ovary Adenocarcinoma 49 0.164
768
c RNG021 Ring Chromosome 5 20 0.164
769
c FML191 Familial Long Qt Syndrome 54 0.164
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