Search results for Tranexamic Acid

472 hits were found for Tranexamic Acid

# Family MCID Name MIFTS Score
1
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.575
2
PLM033 Pulmonary Embolism 59 0.431
3
c THR092 Thrombophilia Due to Thrombin Defect 73 0.396
4
OST012 Osteoarthritis 78 0.387
5
P SZR006 Seizure Disorder 58 0.362
6
THR024 Thrombosis 56 0.350
7
VSL002 Visual Epilepsy 58 0.342
8
P KDN018 Kidney Disease 70 0.332
9
48X005 48,xyyy 39 0.329
10
DFC004 Deficiency Anemia 75 0.323
11
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.316
12
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.314
13
P LVR013 Liver Disease 68 0.312
14
P MYC007 Myocardial Infarction 70 0.288
15
STR067 Stroke, Ischemic 80 0.275
16
CRB039 Cerebrovascular Disease 69 0.269
17
P DRR001 Diarrhea 57 0.268
18
ALL026 Allergic Hypersensitivity Disease 64 0.266
19
LVR012 Liver Cirrhosis 63 0.260
20
TRM010 Traumatic Brain Injury 53 0.240
21
c RHB024 Rhabdomyosarcoma 2 65 0.240
22
ISC004 Ischemia 60 0.239
23
P CLR023 Colorectal Cancer 98 0.235
24
HLX001 Helix Syndrome 47 0.235
25
P VSC007 Vascular Disease 63 0.233
26
BRN071 Brain Injury 49 0.233
27
NRL016 Neural Tube Defects 82 0.232
28
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.228
29
P CRN300 Coronary Heart Disease 1 63 0.225
30
OCL069 Ocular Motor Apraxia 51 0.219
31
MTB004 Metabolic Acidosis 50 0.218
32
P SCL018 Scoliosis 60 0.217
33
ACT119 Acute Promyelocytic Leukemia 63 0.217
34
P BRS047 Breast Cancer 96 0.216
35
PPT005 Peptic Ulcer Disease 58 0.216
36
c CHR684 Chronic Kidney Disease 66 0.214
37
P ART022 Arthritis 70 0.211
38
P NRB001 Neuroblastoma 71 0.210
39
c DWL002 Dowling-Degos Disease 1 58 0.210
40
P CRN018 Coronary Artery Anomaly 63 0.207
41
P ENC018 Encephalopathy 61 0.207
42
P HRT032 Heart Disease 75 0.207
43
P NRF023 Neurofibromatosis, Type Ii 76 0.207
44
ATX019 Ataxia with Vitamin E Deficiency 48 0.206
45
P OVR042 Ovarian Cancer 89 0.205
46
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.204
47
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.197
48
P THR014 Thrombocytopenia 68 0.196
49
c HYP595 Hypertension, Essential 84 0.196
50
P DDN001 Duodenal Ulcer 50 0.194
51
IRN002 Iron Metabolism Disease 57 0.194
52
ART140 Arteries, Anomalies of 53 0.193
53
c PRC016 Pre-Eclampsia 63 0.190
54
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.188
55
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.187
56
GST092 Gastroesophageal Reflux 65 0.184
57
CYS001 Cystic Fibrosis 80 0.184
58
P HPT023 Hepatocellular Carcinoma 100 0.182
59
c ACT071 Acute Kidney Failure 59 0.181
60
P CNR004 Cone-Rod Dystrophy 2 71 0.179
61
CLT003 Colitis 62 0.179
62
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.178
63
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.177
64
P TRN020 Turner Syndrome 65 0.177
65
DRM006 Dermatitis 61 0.173
66
c FNC043 Fanconi Anemia, Complementation Group E 62 0.173
67
ULC004 Ulcerative Colitis 73 0.173
68
P BLD134 Bladder Cancer 78 0.173
69
ATM095 Autoimmune Disease 61 0.172
70
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.172
71
P ART023 Arthropathy 62 0.171
72
c ACT075 Acute Myocardial Infarction 56 0.170
73
P CRD246 Cardiovascular System Disease 56 0.169
74
CYT002 Cytokine Deficiency 44 0.169
75
P CRN037 Craniosynostosis 68 0.167
76
RRD056 Rare Disease in Surgical Orthopedic 28 0.166
77
HYP781 Hypoascorbemia 50 0.165
78
P INF037 Inflammatory Bowel Disease 56 0.165
79
HMN044 Human Immunodeficiency Virus Type 1 71 0.165
80
ADL002 Adult Syndrome 69 0.164
81
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.163
82
RRS014 Rare Surgical Neurologic Disease 32 0.163
83
c GLL024 Gallbladder Disease 1 52 0.162
84
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.161
85
AGN016 Aging 56 0.159
86
P HMP007 Hemophilia 51 0.159
87
TLN003 Telangiectasis 51 0.159
88
P CRD119 Cardiac Arrest 67 0.158
89
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.157
90
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.157
91
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.157
92
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.157
93
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.157
94
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.157
95
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.157
96
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.157
97
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.157
98
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.157
99
NTR005 Nutritional Deficiency Disease 61 0.157
100
DSS009 Disseminated Intravascular Coagulation 57 0.157
101
47X002 47,xyy 49 0.157
102
HPT004 Hepatic Coma 43 0.156
103
END030 End Stage Renal Failure 58 0.155
104
CNG034 Congestive Heart Failure 70 0.153
105
MSS001 Masa Syndrome 62 0.153
106
P RSP003 Respiratory Failure 74 0.152
107
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.151
108
OST003 Osteonecrosis 61 0.151
109
IDP070 Idiopathic Scoliosis 37 0.151
110
P MYL006 Myeloid Leukemia 60 0.150
111
ADN018 Adenoma 58 0.150
112
ANR040 Aneurysm 58 0.149
113
LMY002 Leiomyoma 50 0.148
114
HPT019 Hepatic Encephalopathy 60 0.147
115
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.146
116
LNG099 Lung Disease 61 0.144
117
ACT058 Active Peptic Ulcer Disease 55 0.144
118
c LKM061 Leukemia, Acute Myeloid 83 0.142
119
P EPL164 Epilepsy 71 0.142
120
GST023 Gastric Ulcer 53 0.141
121
P GST053 Gastric Cancer 83 0.141
122
PNG002 Pain Agnosia 51 0.141
123
P ECL001 Eclampsia 51 0.141
124
ANG054 Angina Pectoris 66 0.140
125
P NTR004 Neutropenia 63 0.139
126
P DRM053 Dermatitis, Atopic 66 0.138
127
P BPL003 Bipolar Disorder 56 0.137
128
P RHM011 Rheumatoid Arthritis 80 0.137
129
c MJR024 Major Affective Disorder 9 41 0.137
130
c MJR022 Major Affective Disorder 8 38 0.137
131
P ADL010 Adult Respiratory Distress Syndrome 63 0.136
132
CHL079 Children's Interstitial Lung Disease 27 0.136
133
DWN001 Down Syndrome 70 0.134
134
HDN002 Head Injury 45 0.134
135
MLN073 Melanosis, Neurocutaneous 45 0.133
136
HYP266 Hypoxia 56 0.132
137
HMR002 Hemarthrosis 45 0.132
138
SKN016 Skin Disease 63 0.132
139
STT001 Status Epilepticus 59 0.131
140
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.130
141
PRP027 Peripheral Vascular Disease 71 0.130
142
PRS045 Prostatic Hypertrophy 52 0.130
143
P HDC001 Headache 57 0.130
144
URM002 Uremia 49 0.130
145
CLF027 Cleft Palate, Isolated 64 0.130
146
TXC005 Toxic Shock Syndrome 61 0.129
147
P CTR002 Cataract 60 0.128
148
P ATS364 Autism 65 0.127
149
c ACT068 Acute Cystitis 63 0.127
150
c HRD002 Hereditary Angioedema 61 0.126
151
PRS021 Prostatic Adenoma 51 0.126
152
BRN024 Bronchitis 68 0.125
153
PLM010 Pulmonary Edema 55 0.125
154
P HRP006 Herpes Simplex 65 0.125
155
BCT022 Bacterial Infectious Disease 56 0.124
156
P URT039 Urticaria 58 0.123
157
P PNM007 Pneumonia 68 0.123
158
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.123
159
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.123
160
P ANG015 Angioedema 54 0.123
161
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.122
162
GST033 Gestational Diabetes 57 0.122
163
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.122
164
P MNN013 Meningitis 65 0.121
165
P EXN002 Exanthem 57 0.121
166
P SCL057 Scoliosis, Isolated 1 41 0.121
167
PLC009 Placenta Praevia 37 0.121
168
TRN015 Transient Cerebral Ischemia 62 0.120
169
PRP030 Purpura 55 0.120
170
FCT001 Factor Viii Deficiency 55 0.120
171
P HPT021 Hepatitis 67 0.119
172
P AST007 Astrocytoma 50 0.118
173
PRS129 Prostatic Hyperplasia, Benign 49 0.118
174
c HPT001 Hepatitis C 63 0.118
175
CRT017 Cartilage Disease 54 0.118
176
P HYP086 Hypothyroidism 68 0.118
177
SPN186 Spinal Cord Injury 60 0.118
178
RHM027 Rheumatic Disease 56 0.117
179
SQM006 Squamous Cell Carcinoma 60 0.116
180
VRC005 Varicose Veins 60 0.115
181
RSC001 Rosacea 55 0.115
182
P HYD006 Hydrocephalus 65 0.115
183
PLC007 Placental Abruption 48 0.115
184
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.115
185
MLN008 Melanoma 69 0.114
186
P ATR011 Atrial Fibrillation 66 0.114
187
MYM001 Myoma 53 0.114
188
c MGR028 Migraine with or Without Aura 1 69 0.113
189
MYF001 Myofibroma 42 0.112
190
ART016 Aortic Aneurysm 68 0.112
191
P MSC005 Muscular Dystrophy 66 0.112
192
HMR039 Hemorrhage, Intracerebral 57 0.111
193
ACQ007 Acquired Immunodeficiency Syndrome 60 0.111
194
c PNS012 Paine Syndrome 61 0.109
195
IRN001 Iron Deficiency Anemia 58 0.109
196
c LRG017 Large Intestine Cancer 47 0.108
197
CMM005 Common Cold 56 0.108
198
P SCH015 Schizophrenia 75 0.108
199
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.107
200
P VNW001 Von Willebrand's Disease 64 0.107
201
P SCK005 Sickle Cell Disease 50 0.106
202
PRT013 Portal Hypertension 60 0.106
203
P MYC084 Mycobacterium Tuberculosis 1 68 0.106
204
P SKN015 Skin Carcinoma 67 0.106
205
c HMP029 Hemophilia a 65 0.105
206
HYP005 Hypokalemia 55 0.104
207
INT007 Intermediate Coronary Syndrome 55 0.104
208
EYD002 Eye Disease 58 0.103
209
SPN027 Spinal Stenosis 59 0.103
210
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.103
211
P LPS004 Lupus Erythematosus 61 0.103
212
P PLY014 Polycystic Kidney Disease 59 0.102
213
P GLM040 Glioma Susceptibility 1 81 0.102
214
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.102
215
c ANG068 Angioedema, Hereditary, Type I 56 0.101
216
P NRV007 Nervous System Disease 66 0.101
217
PPL022 Papilloma 54 0.101
218
MNN042 Meningioma, Radiation-Induced 62 0.100
219
c MNN043 Meningioma, Familial 74 0.100
220
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.100
221
P BLD051 Blood Coagulation Disease 46 0.100
222
c CRN278 Craniosynostosis 1 45 0.100
223
SPN021 Spinal Meningioma 47 0.099
224
SCR001 Secretory Meningioma 37 0.099
225
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.099
226
BRN028 Brain Cancer 73 0.099
227
ISL062 Isolated Plagiocephaly 35 0.099
228
P MYC033 Myoclonus 46 0.099
229
P MCR115 Microvascular Complications of Diabetes 5 66 0.098
230
P CYS018 Cystitis 59 0.098
231
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.098
232
c ACT073 Acute Leukemia 58 0.098
233
ANX010 Anxiety 72 0.098
234
P INF038 Influenza 68 0.097
235
SQM002 Squamous Cell Papilloma 42 0.097
236
CNT047 Contact Dermatitis 57 0.097
237
LPT014 Leptin Deficiency or Dysfunction 73 0.097
238
CNS004 Constipation 57 0.096
239
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.096
240
P CHR345 Chronic Pain 50 0.096
241
P INF032 Infertility 57 0.096
242
SCH014 Schistosomiasis 56 0.095
243
P PLM037 Pulmonary Hypertension 68 0.095
244
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.095
245
c BRN108 Branchiootic Syndrome 1 61 0.095
246
P AMY004 Amyloidosis 70 0.094
247
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.094
248
PLC008 Placenta Disease 49 0.093
249
P CNJ013 Conjunctivitis 65 0.093
250
c OVR114 Ovarian Cancer 1 38 0.093
251
P INT143 Interstitial Cystitis 61 0.093
252
P HMR003 Hemorrhagic Disease 52 0.092
253
LMY014 Leiomyoma, Uterine 56 0.092
254
c CNT035 Central Nervous System Disease 54 0.091
255
P BRN022 Bronchiectasis 59 0.091
256
P LNG064 Lung Cancer Susceptibility 3 77 0.091
257
ACR041 Acromelic Frontonasal Dysostosis 52 0.090
258
P THR015 Thrombophilia 50 0.090
259
TRN018 Transitional Cell Carcinoma 56 0.089
260
c CHR682 Chronic Bilirubin Encephalopathy 38 0.087
261
ATS010 Autosomal Recessive Disease 48 0.085
262
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.085
263
SCK003 Sickle Cell Anemia 72 0.085
264
P BNC003 Bone Cancer 57 0.085
265
P HMN010 Hemangioma 61 0.085
266
RTN023 Retinitis 46 0.084
267
NRR001 Neuroretinitis 43 0.084
268
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.084
269
P PRC031 Preeclampsia/eclampsia 1 37 0.084
270
P RTN016 Retinal Degeneration 53 0.084
271
P OCL013 Oculodentodigital Dysplasia 69 0.084
272
SBC016 Subacute Delirium 44 0.083
273
BLD053 Blood Platelet Disease 51 0.083
274
THR016 Thrombophlebitis 51 0.083
275
PST092 Posttransplant Acute Limbic Encephalitis 29 0.083
276
c FML001 Familial Atrial Fibrillation 66 0.082
277
P END033 Endocarditis 57 0.082
278
c LKM063 Leukemia, Chronic Myeloid 71 0.082
279
KRT013 Keratolytic Winter Erythema 46 0.082
280
c BSL007 Basal Cell Carcinoma 68 0.082
281
49X006 49, Xxxxy Syndrome 41 0.081
282
MSC157 Muscular Dystrophy, Duchenne Type 71 0.081
283
HMT002 Hematologic Cancer 62 0.081
284
PLY012 Polyhydramnios 46 0.081
285
ESP002 Esophageal Varix 51 0.080
286
ALL010 Allergic Contact Dermatitis 55 0.080
287
P BNG032 Benign Mesothelioma 45 0.079
288
CYN002 Cyanosis, Transient Neonatal 45 0.079
289
HRT011 Heart Septal Defect 50 0.079
290
LNT004 Lentigines 46 0.078
291
VTM033 Vitamin K Deficiency Bleeding 48 0.078
292
PSY004 Psychotic Disorder 67 0.078
293
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 39 0.077
294
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.076
295
ILS001 Ileus 51 0.076
296
HPT014 Hepatorenal Syndrome 50 0.076
297
HLL004 Hellp Syndrome 53 0.076
298
P TRC086 Trichohepatoenteric Syndrome 1 59 0.076
299
SPN041 Spinal Cord Disease 56 0.076
300
PLC001 Placenta Accreta 44 0.076
301
CRC006 Carcinoid Syndrome 55 0.076
302
STP011 Stapes Ankylosis with Broad Thumbs and Toes 48 0.075
303
RDN001 Reading Disorder 40 0.075
304
CRB037 Cerebral Palsy 68 0.074
305
P HML002 Hemolytic Anemia 62 0.074
306
GNG013 Gingivitis 59 0.074
307
MCR013 Microphthalmia 60 0.074
308
P VNT002 Ventricular Septal Defect 60 0.073
309
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.073
310
c MCR129 Microvascular Complications of Diabetes 1 66 0.072
311
NWB001 Newborn Respiratory Distress Syndrome 58 0.072
312
TRP009 Triple X Syndrome 42 0.071
313
P VSC011 Vasculitis 62 0.070
314
CRC014 Carcinoid Tumors, Intestinal 48 0.069
315
FXD003 Fixed Drug Eruption 35 0.069
316
P MJR007 Major Affective Disorder 1 43 0.068
317
C1N001 C1 Inhibitor Deficiency 40 0.068
318
OVR094 Ovarian Epithelial Cancer 38 0.068
319
P CRB088 Cerebral Atrophy 38 0.067
320
WBR001 Weber Syndrome 34 0.067
321
c XNT010 Xanthinuria, Type I 50 0.067
322
P TTR001 Tetralogy of Fallot 69 0.067
323
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.067
324
CHR005 Chorioamnionitis 51 0.066
325
P AVS003 Avascular Necrosis 42 0.066
326
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.066
327
GST020 Gastric Antral Vascular Ectasia 41 0.065
328
CMP040 Complement Component 4, Partial Deficiency of 33 0.065
329
INT030 Intracranial Aneurysm 56 0.065
330
c MJR003 Major Affective Disorder 6 33 0.065
331
c MJR006 Major Affective Disorder 5 33 0.065
332
c BCT007 Bacterial Meningitis 55 0.064
333
c MJR008 Major Affective Disorder 2 34 0.064
335
c MJR023 Major Affective Disorder 7 33 0.064
336
c MJR004 Major Affective Disorder 4 28 0.064
337
HMN035 Hemangioma-Thrombocytopenia Syndrome 41 0.063
338
MST004 Mast Cell Neoplasm 38 0.063
339
EXT007 Extracutaneous Mastocytoma 38 0.063
340
THR035 Thrombasthenia 41 0.063
341
INT017 Intestinal Schistosomiasis 47 0.063
342
CRD001 Cardiac Tamponade 46 0.063
343
NTR018 Neutrophilia, Hereditary 52 0.062
344
P RTN014 Retinal Artery Occlusion 46 0.061
345
BRN026 Branch Retinal Artery Occlusion 43 0.061
346
P PLV020 Pelvic Organ Prolapse 59 0.061
347
ACT003 Acute Kidney Tubular Necrosis 45 0.060
348
c MLG074 Malignant Mesenchymoma 39 0.060
349
APH002 Aphasia 57 0.060
350
FTL021 Fetal Macrosomia 42 0.060
351
KDN001 Kidney Cortex Necrosis 32 0.060
352
MDS022 Mediastinitis 47 0.059
353
BCK006 Back Pain 42 0.059
354
HMG005 Hemoglobinopathy 55 0.059
355
c MCR112 Microvascular Complications of Diabetes 2 41 0.059
356
P BRN120 Bronchus Cancer 42 0.059
357
P DVL012 Developmental Dysplasia of the Hip 1 30 0.059
358
BRN053 Bronchial Adenomas/carcinoids Childhood 25 0.059
359
c CNG216 Congenital Hydrocephalus 50 0.059
360
c MST023 Mesothelioma, Malignant 57 0.058
361
INT067 Interstitial Nephritis 46 0.058
362
HMP005 Hemiplegia 54 0.058
363
MCN017 Meconium Ileus 52 0.058
364
ECT026 Ectopic Pregnancy 49 0.058
365
SPT004 Septic Arthritis 57 0.058
366
P ART005 Arteriovenous Malformation 65 0.057
367
INT078 Intracranial Thrombosis 48 0.057
368
P CMP008 Compartment Syndrome 48 0.057
369
STL007 Steel Syndrome 42 0.057
370
SPC030 Specific Language Disorder 26 0.057
371
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.057
372
P PLM034 Pulmonary Emphysema 56 0.057
373
P RSS029 Resistance to Thyroid Hormone Due to a Mutation in Thyroid Hormone Receptor Alpha 16 0.057
374
PRL032 Perlman Syndrome 58 0.056
375
BNN005 Bunion 33 0.056
376
c DPH024 Diaphragmatic Hernia, Congenital 64 0.056
377
MCL006 Macular Retinal Edema 55 0.056
378
P ATR010 Atrial Heart Septal Defect 60 0.056
379
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 0.056
380
ANR004 Anuria 46 0.055
381
CRB086 Cerebral Aneurysms 40 0.055
382
RTN020 Retinal Vascular Disease 48 0.055
383
AFB002 Afibrinogenemia, Congenital 65 0.055
384
P ACH003 Achromatopsia 60 0.055
385
GLN010 Glanzmann Thrombasthenia 66 0.054
386
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.054
387
c ALM001 Al Amyloidosis 50 0.054
388
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.054
389
P CLR019 Color Blindness 48 0.054
390
BHR001 Behr Syndrome 49 0.053
391
URN010 Urinary Tract Obstruction 57 0.053
392
GSG001 Gas Gangrene 50 0.053
393
CYS014 Cystadenocarcinoma 51 0.053
394
DYS165 Dysfibrinogenemia, Congenital 52 0.053
395
SPN369 Spinal Disease 41 0.053
396
THR017 Thoracoabdominal Syndrome 39 0.053
397
P PMP001 Pemphigus 55 0.052
398
BNN003 Bone Inflammation Disease 48 0.052
399
INT146 Intervertebral Disc Disease 62 0.052
400
CRT072 Creutzfeldt-Jakob Disease 69 0.052
401
c ACH020 Achromatopsia 2 50 0.052
402
BKS003 Beukes Hip Dysplasia 39 0.052
403
OVR060 Ovary Epithelial Cancer 33 0.052
404
BRN008 Brain Compression 29 0.052
405
c MCL013 Mucolipidosis Iv 64 0.052
406
P HML001 Hemolytic-Uremic Syndrome 52 0.052
407
INF034 Infective Endocarditis 52 0.051
408
SRS001 Serous Cystadenocarcinoma 52 0.051
409
c CNT028 Central Retinal Artery Occlusion 43 0.051
410
P PRC012 Pericardial Effusion 51 0.051
411
HMP001 Hemopericardium 46 0.051
412
c VNW005 Von Willebrand Disease, Type 1 49 0.050
413
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.050
414
SVR097 Severe Cutaneous Adverse Reaction 67 0.050
415
CRD137 Cardiogenic Shock 48 0.049
416
VGN019 Vaginal Discharge 44 0.049
417
LGN005 Ligneous Conjunctivitis 40 0.049
418
ASP003 Aseptic Meningitis 51 0.049
419
c ART101 Aortic Valve Disease 2 63 0.048
420
CNN003 Conn's Syndrome 79 0.047
421
P ART018 Aortic Valve Insufficiency 53 0.047
422
HMR023 Hemorrhagic Cystitis 38 0.047
423
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.046
424
CRB079 Cerebrospinal Fluid Leak 35 0.045
425
DRG024 Drug Allergy 43 0.045
426
PTN001 Patent Foramen Ovale 56 0.044
427
ANG049 Angioedema Induced by Ace Inhibitors 40 0.044
428
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.043
429
TNG003 Tongue Cancer 55 0.043
430
P RTN022 Retinal Vein Occlusion 52 0.043
431
SYN005 Synostosis 45 0.043
432
BRN034 Brain Meningioma 33 0.043
433
TNG009 Tongue Squamous Cell Carcinoma 44 0.043
434
c HMP004 Hemophilia B 67 0.042
435
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.040
436
c ACQ014 Acquired Hemophilia 45 0.040
437
END051 Endolymphatic Sac Tumor 28 0.040
438
P ORT004 Orthostatic Intolerance 63 0.039
439
HPT046 Hepatic Veno-Occlusive Disease 56 0.039
440
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.039
441
SPN019 Spondylolisthesis 49 0.039
442
THR123 Thrombotic Microangiopathy 38 0.039
443
DFF031 Diffuse Alveolar Hemorrhage 26 0.039
444
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.038
445
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.038
446
ALV001 Alveolar Periostitis 31 0.038
447
PPL058 Papilloma of Choroid Plexus 57 0.036
448
CYT005 Cytomegalovirus Retinitis 49 0.036
449
IMM064 Immunodeficiency, Common Variable, 10 44 0.036
450
KND001 Kindler Syndrome 63 0.035
451
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 45 0.035
452
HYP855 Hyperpigmentation of the Skin 27 0.035
453
CRM001 Crimean-Congo Hemorrhagic Fever 52 0.033
454
P CPL006 Capillary Hemangioma 51 0.033
455
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.033
456
c CPL013 Capillary Malformations, Congenital 40 0.033
457
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.033
458
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.032
459
ANR009 Aneurysmal Bone Cysts 43 0.032
460
SMT002 Smooth Muscle Tumor 37 0.032
461
FCT002 Factor Xi Deficiency 59 0.030
462
PRT014 Protein S Deficiency 50 0.030
463
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 44 0.030
464
ANG011 Angiodysplasia 43 0.030
465
IMM154 Immunoglobulin a Deficiency 1 43 0.030
466
OVR047 Ovarian Cystadenocarcinoma 35 0.030
467
ANG062 Angioosteohypertrophic Syndrome 33 0.030
468
ANS006 Anosognosia 29 0.030
469
GNT005 Giant Hemangioma 27 0.030
470
FCT003 Factor X Deficiency 55 0.028
471
EVN001 Evans' Syndrome 46 0.028
472
c ACQ012 Acquired Angioedema 39 0.028
Content
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