Search results for Misoprostol

343 hits were found for Misoprostol

# Family MCID Name MIFTS Score
1
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.487
2
48X005 48,xyyy 39 0.353
3
P DRR001 Diarrhea 57 0.350
4
P DDN001 Duodenal Ulcer 50 0.280
5
GST023 Gastric Ulcer 53 0.247
6
PPT005 Peptic Ulcer Disease 58 0.240
7
CHR005 Chorioamnionitis 51 0.237
8
c PRC016 Pre-Eclampsia 63 0.235
9
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.218
10
P CNR004 Cone-Rod Dystrophy 2 71 0.210
11
AMN001 Amenorrhea 54 0.210
12
P ECL001 Eclampsia 51 0.182
13
LMY002 Leiomyoma 50 0.182
14
PNG002 Pain Agnosia 51 0.178
15
c RHB024 Rhabdomyosarcoma 2 65 0.175
16
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.171
17
c PNS012 Paine Syndrome 61 0.164
18
P INF032 Infertility 57 0.164
19
P HDC001 Headache 57 0.160
20
ATX019 Ataxia with Vitamin E Deficiency 48 0.160
21
DFC004 Deficiency Anemia 75 0.156
22
P PRC031 Preeclampsia/eclampsia 1 37 0.156
23
DWN001 Down Syndrome 70 0.148
24
MYM001 Myoma 53 0.140
25
ALL026 Allergic Hypersensitivity Disease 64 0.135
26
P END046 Endometritis 47 0.135
27
MYF001 Myofibroma 42 0.135
28
OST012 Osteoarthritis 78 0.131
29
ECT026 Ectopic Pregnancy 49 0.131
30
49X006 49, Xxxxy Syndrome 41 0.131
31
c HYP595 Hypertension, Essential 84 0.126
32
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.126
33
LMY014 Leiomyoma, Uterine 56 0.126
34
P GST044 Gastritis 55 0.126
35
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.126
36
PLC009 Placenta Praevia 37 0.126
37
CHL079 Children's Interstitial Lung Disease 27 0.126
38
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.121
39
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.121
40
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.121
41
PLC007 Placental Abruption 48 0.121
42
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.121
43
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.121
44
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.121
45
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.121
46
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.121
47
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.121
48
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.121
49
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.121
50
IRN002 Iron Metabolism Disease 57 0.116
51
GST033 Gestational Diabetes 57 0.111
52
MBS002 Moebius Syndrome 57 0.111
53
ASP004 Asphyxia Neonatorum 45 0.111
54
CYT002 Cytokine Deficiency 44 0.111
55
GST020 Gastric Antral Vascular Ectasia 41 0.111
56
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.105
57
PLY012 Polyhydramnios 46 0.105
58
HRW001 Hair Whorl 36 0.105
59
P INT143 Interstitial Cystitis 61 0.099
60
ISC004 Ischemia 60 0.099
61
OLG003 Oligohydramnios 52 0.099
62
P UTR058 Uterine Anomalies 48 0.099
63
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.092
64
CNS004 Constipation 57 0.092
65
c SVR005 Severe Pre-Eclampsia 49 0.092
66
c SPN225 Spondyloarthropathy 1 73 0.086
67
SPN051 Spondylitis 52 0.086
68
BWN001 Bowen-Conradi Syndrome 51 0.086
69
PLC008 Placenta Disease 49 0.086
70
47X002 47,xyy 49 0.086
71
RDN001 Reading Disorder 40 0.086
72
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.086
73
INF009 Inflammatory Spondylopathy 32 0.086
74
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.086
75
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.078
76
P KDN018 Kidney Disease 70 0.078
77
P ART022 Arthritis 70 0.078
78
ANG054 Angina Pectoris 66 0.078
79
LVR012 Liver Cirrhosis 63 0.078
80
P CRN018 Coronary Artery Anomaly 63 0.078
81
P CRN300 Coronary Heart Disease 1 63 0.078
82
TXC005 Toxic Shock Syndrome 61 0.078
83
ACQ007 Acquired Immunodeficiency Syndrome 60 0.078
84
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.078
85
MCS002 Mucositis 55 0.078
86
ACT058 Active Peptic Ulcer Disease 55 0.078
87
HLL004 Hellp Syndrome 53 0.078
88
ART140 Arteries, Anomalies of 53 0.078
89
HYP781 Hypoascorbemia 50 0.078
90
SYN036 Syncope 45 0.078
91
END080 Endometrial Disease 45 0.078
92
PLC001 Placenta Accreta 44 0.078
93
HYP679 Hypoglossia-Hypodactylia 34 0.078
94
CRV025 Cervical Incompetence 33 0.078
95
CHR159 Charlie M Syndrome 24 0.078
96
CYS001 Cystic Fibrosis 80 0.070
97
P RHM011 Rheumatoid Arthritis 80 0.070
98
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.070
99
PRP027 Peripheral Vascular Disease 71 0.070
100
HMN044 Human Immunodeficiency Virus Type 1 71 0.070
101
P VSC007 Vascular Disease 63 0.070
102
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.070
103
c FNC043 Fanconi Anemia, Complementation Group E 62 0.070
104
CLT003 Colitis 62 0.070
105
IRN001 Iron Deficiency Anemia 58 0.070
106
PRL032 Perlman Syndrome 58 0.070
107
DSS009 Disseminated Intravascular Coagulation 57 0.070
108
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.070
109
ACR041 Acromelic Frontonasal Dysostosis 52 0.070
110
NTR018 Neutrophilia, Hereditary 52 0.070
111
VGN019 Vaginal Discharge 44 0.070
112
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.070
113
FTL021 Fetal Macrosomia 42 0.070
114
P PRG092 Pregnancy Loss, Recurrent 1 40 0.070
115
c SYS001 Systemic Lupus Erythematosus 86 0.061
116
P HRT032 Heart Disease 75 0.061
117
CRH001 Crohn's Disease 74 0.061
118
P MYC007 Myocardial Infarction 70 0.061
119
P THR014 Thrombocytopenia 68 0.061
120
P CRD119 Cardiac Arrest 67 0.061
121
c FML001 Familial Atrial Fibrillation 66 0.061
122
P ATR011 Atrial Fibrillation 66 0.061
123
P HYD006 Hydrocephalus 65 0.061
124
P TRN020 Turner Syndrome 65 0.061
125
c MCL013 Mucolipidosis Iv 64 0.061
126
GT001 Gout 63 0.061
127
P END044 Endometriosis 62 0.061
128
P ENC018 Encephalopathy 61 0.061
129
P CYS018 Cystitis 59 0.061
130
c HPT016 Hepatitis B 59 0.061
131
HLC007 Helicobacter Pylori Infection 59 0.061
132
P SZR006 Seizure Disorder 58 0.061
133
VSL002 Visual Epilepsy 58 0.061
134
NWB001 Newborn Respiratory Distress Syndrome 58 0.061
135
BRN056 Bronchopulmonary Dysplasia 57 0.061
136
P EXN002 Exanthem 57 0.061
137
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.061
138
HYP266 Hypoxia 56 0.061
139
P ALP008 Alopecia 56 0.061
140
P CRD246 Cardiovascular System Disease 56 0.061
141
BRN004 Brain Edema 55 0.061
142
HYP005 Hypokalemia 55 0.061
143
P INT068 Intestinal Disease 52 0.061
144
c VRL010 Viral Hepatitis 51 0.061
145
HPT014 Hepatorenal Syndrome 50 0.061
146
BHR001 Behr Syndrome 49 0.061
147
HYP068 Hyperostosis 48 0.061
148
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.061
149
FCL012 Facial Paralysis 48 0.061
150
CLS016 Clostridium Difficile Colitis 46 0.061
151
CRN019 Coronary Artery Vasospasm 46 0.061
152
GST010 Gestational Trophoblastic Neoplasm 46 0.061
153
ALK024 Alkuraya-Kucinskas Syndrome 43 0.061
154
LTX001 Latex Allergy 43 0.061
155
TRP009 Triple X Syndrome 42 0.061
156
BCK006 Back Pain 42 0.061
157
FML039 Female Reproductive System Disease 38 0.061
158
SBM005 Submucous Uterine Fibroid 30 0.061
159
RSP007 Respiratory Distress Syndrome, Infant 30 0.061
160
CYT018 Cytochrome P450 2d6 Variant 27 0.061
161
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.061
162
CNG506 Congenital Amyoplasia 25 0.061
163
NRL016 Neural Tube Defects 82 0.049
164
STR067 Stroke, Ischemic 80 0.049
165
SVR004 Severe Combined Immunodeficiency 73 0.049
166
P OST002 Osteoporosis 73 0.049
167
c THR092 Thrombophilia Due to Thrombin Defect 73 0.049
168
ANX010 Anxiety 72 0.049
169
P NRB001 Neuroblastoma 71 0.049
170
CRB039 Cerebrovascular Disease 69 0.049
171
P HLP001 Holoprosencephaly 68 0.049
172
c CHR684 Chronic Kidney Disease 66 0.049
173
P CNJ013 Conjunctivitis 65 0.049
174
CLF027 Cleft Palate, Isolated 64 0.049
175
IRR002 Irritable Bowel Syndrome 63 0.049
176
c ACT068 Acute Cystitis 63 0.049
177
P ESP024 Esophagitis 62 0.049
178
c BRN108 Branchiootic Syndrome 1 61 0.049
179
ATM095 Autoimmune Disease 61 0.049
180
HPT019 Hepatic Encephalopathy 60 0.049
181
CHR619 Chromosome 2q35 Duplication Syndrome 60 0.049
182
TRG002 Trigeminal Neuralgia 60 0.049
183
P ALP009 Alopecia Areata 60 0.049
184
GNG013 Gingivitis 59 0.049
185
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.049
186
ADN018 Adenoma 58 0.049
187
P RHN004 Rhinitis 57 0.049
188
PLM010 Pulmonary Edema 55 0.049
189
PRT082 Preterm Premature Rupture of the Membranes 54 0.049
190
P TRM003 Tremor 53 0.049
191
HMT008 Hematuria, Benign Familial 53 0.049
192
KRT009 Keratosis 53 0.049
193
NNT012 Neonatal Jaundice 53 0.049
194
MCN007 Meconium Aspiration Syndrome 52 0.049
195
PPT001 Peptic Esophagitis 51 0.049
196
DYS073 Dysphagia 50 0.049
197
SXL003 Sexual Disorder 48 0.049
198
END062 Endometrial Hyperplasia 48 0.049
199
RDT013 Radiation Proctitis 47 0.049
200
P ENC008 Encephalocele 47 0.049
201
CLB002 Clubfoot 47 0.049
202
PRC003 Proctitis 47 0.049
203
RYN005 Raynaud Phenomenon 46 0.049
204
PLN006 Poland Syndrome 46 0.049
205
P OCY003 Oocyte Maturation Defect 1 45 0.049
206
SBC016 Subacute Delirium 44 0.049
207
HPT004 Hepatic Coma 43 0.049
208
P HYP265 Hypotonia 42 0.049
209
ACT011 Acute Contagious Conjunctivitis 40 0.049
210
HMR023 Hemorrhagic Cystitis 38 0.049
211
HMM005 Hemimelia 36 0.049
212
ASH001 Asherman's Syndrome 32 0.049
213
FBL014 Fibular Hemimelia 28 0.049
214
BCR002 Bicornuate Uterus 24 0.049
215
P CLR023 Colorectal Cancer 98 0.035
216
P BRS047 Breast Cancer 96 0.035
217
P ALZ034 Alzheimer Disease 88 0.035
218
INS024 Insulin-Like Growth Factor I 79 0.035
219
IMM167 Immune Deficiency Disease 78 0.035
220
AST005 Asthma 77 0.035
221
GST019 Gastrointestinal Stromal Tumor 76 0.035
222
CRV035 Cervical Cancer 76 0.035
223
END057 Endometrial Cancer 74 0.035
224
ULC004 Ulcerative Colitis 73 0.035
225
P MLT020 Multiple Sclerosis 72 0.035
226
P GRF003 Graft-Versus-Host Disease 71 0.035
227
c LKM063 Leukemia, Chronic Myeloid 71 0.035
228
P LVR013 Liver Disease 68 0.035
229
P PLM037 Pulmonary Hypertension 68 0.035
230
P CRN037 Craniosynostosis 68 0.035
231
c ATS007 Autism Spectrum Disorder 67 0.035
232
P HPT021 Hepatitis 67 0.035
233
ALL003 Allergic Rhinitis 67 0.035
234
ABT001 Abetalipoproteinemia 67 0.035
235
SVR097 Severe Cutaneous Adverse Reaction 67 0.035
236
P DRM053 Dermatitis, Atopic 66 0.035
237
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.035
238
c HMP029 Hemophilia a 65 0.035
239
PRT037 Pertussis 65 0.035
240
P HRP006 Herpes Simplex 65 0.035
241
TTN003 Tetanus 64 0.035
242
P NPH012 Nephrotic Syndrome 63 0.035
243
INT146 Intervertebral Disc Disease 62 0.035
244
P ART023 Arthropathy 62 0.035
245
P HML002 Hemolytic Anemia 62 0.035
246
P VSC011 Vasculitis 62 0.035
247
FTT001 Fatty Liver Disease 61 0.035
248
HYP066 Hyperglycemia 61 0.035
249
P LPS004 Lupus Erythematosus 61 0.035
250
PRT013 Portal Hypertension 60 0.035
251
P CTR002 Cataract 60 0.035
252
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.035
253
P PTN014 Patent Ductus Arteriosus 1 60 0.035
254
P THL005 Thalassemia 60 0.035
255
c ACT027 Acute Pancreatitis 59 0.035
256
CHL123 Chlamydia 59 0.035
257
PLM033 Pulmonary Embolism 59 0.035
258
SPN027 Spinal Stenosis 59 0.035
259
P BRS044 Breast Adenocarcinoma 59 0.035
260
END030 End Stage Renal Failure 58 0.035
261
ERY003 Erythema Multiforme 57 0.035
262
P GLM007 Glomerulonephritis 57 0.035
263
c ACT075 Acute Myocardial Infarction 56 0.035
264
AVN001 Avian Influenza 56 0.035
265
RHM027 Rheumatic Disease 56 0.035
266
GST050 Gastrointestinal System Disease 56 0.035
267
PRP030 Purpura 55 0.035
268
ANN002 Anencephaly 55 0.035
269
PLV003 Pelvic Inflammatory Disease 55 0.035
270
CHL014 Cholera 55 0.035
271
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.035
272
FCT001 Factor Viii Deficiency 55 0.035
273
VGN023 Vaginitis 55 0.035
274
NRG002 Neurogenic Bladder 54 0.035
275
P PTT006 Pituitary Adenoma 54 0.035
276
PRC013 Pericarditis 54 0.035
277
FRZ001 Frozen Shoulder 53 0.035
278
CHR100 Chronic Ulcer of Skin 53 0.035
279
ALC009 Alcoholic Liver Cirrhosis 53 0.035
280
OCL006 Ocular Hypertension 53 0.035
281
CLF001 Cleft Lip 53 0.035
282
CRH005 Crohn's Colitis 52 0.035
283
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.035
284
BCT002 Bacterial Vaginosis 52 0.035
285
TND005 Tendinitis 52 0.035
286
IMP005 Impotence 52 0.035
287
P HMP007 Hemophilia 51 0.035
288
c ACT135 Acute Graft Versus Host Disease 51 0.035
289
ILS001 Ileus 51 0.035
290
MYL020 Myelomeningocele 51 0.035
291
NNL006 Non-Alcoholic Steatohepatitis 51 0.035
292
ILT001 Ileitis 50 0.035
293
HYP748 Hypertelorism 50 0.035
294
P OVR082 Overgrowth Syndrome 50 0.035
295
MTB004 Metabolic Acidosis 50 0.035
296
P OMP004 Omphalocele 50 0.035
297
BNR002 Bone Resorption Disease 48 0.035
298
P BRS053 Breast Fibroadenoma 48 0.035
299
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.035
300
DGN001 Degenerative Disc Disease 48 0.035
301
PRP007 Priapism 48 0.035
302
BRS064 Bursitis 47 0.035
303
HYP025 Hyperphosphatemia 47 0.035
304
P PRN026 Porencephaly 47 0.035
305
P ERY008 Erythromelalgia 47 0.035
306
c HYD064 Hydrocephalus, Congenital, 1 47 0.035
307
LYM019 Lymphosarcoma 47 0.035
308
URT010 Ureteral Obstruction 46 0.035
309
EXS017 Exstrophy of Bladder 46 0.035
310
OBS004 Obstructive Hydrocephalus 45 0.035
311
RTR008 Root Resorption 45 0.035
312
CRB004 Cerebral Artery Occlusion 44 0.035
313
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 44 0.035
314
FBR054 Fibroma 44 0.035
315
DRG024 Drug Allergy 43 0.035
316
HPT067 Hepatocellular Adenoma 43 0.035
317
ILC002 Ileocolitis 43 0.035
318
PRS063 Paresthesia 43 0.035
319
SPC005 Speech Disorder 42 0.035
320
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.035
321
c DNR003 Duane Retraction Syndrome 1 41 0.035
322
P RRT020 Rare Tumor 41 0.035
323
IMM001 Immune-Complex Glomerulonephritis 39 0.035
324
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.035
325
TRP005 Trophoblastic Neoplasm 38 0.035
326
SKN023 Skin Tag 38 0.035
327
CNS013 Constricting Bands, Congenital 34 0.035
329
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.035
330
DDN004 Duodenogastric Reflux 32 0.035
331
VLV008 Vulvitis 31 0.035
332
OCC011 Occipital Encephalocele 28 0.035
333
CHR280 Chronic Erosive Gastritis 28 0.035
334
ERY066 Erythema Multiforme Major 28 0.035
335
PRT086 Partial Hydatidiform Mole 26 0.035
336
ABD009 Abducens Palsy 24 0.035
337
EXR007 Exercise-Induced Anaphylaxis 23 0.035
338
ABR001 Aberrant Subclavian Artery 22 0.035
339
HML018 Homologous Wasting Disease 22 0.035
340
UNL015 Unilateral Aplasia of the Mullerian Ducts 18 0.035
341
CNG529 Congenital Femoral Deficiency 16 0.035
343
CLS033 Clostridium Sordellii Infection 9 0.035
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