Search results for Coagulation Factor IX (Recombinant)

687 hits were found for Coagulation Factor IX (Recombinant)

# Family MCID Name MIFTS Score
1
P HMP007 Hemophilia 51 0.844
2
DSS009 Disseminated Intravascular Coagulation 57 0.619
3
c HMP004 Hemophilia B 68 0.594
4
c HMP029 Hemophilia a 67 0.556
5
P THR014 Thrombocytopenia 67 0.403
6
c THR092 Thrombophilia Due to Thrombin Defect 73 0.375
7
THR024 Thrombosis 57 0.374
8
P NTR004 Neutropenia 63 0.371
9
P KDN018 Kidney Disease 72 0.356
10
P BRS047 Breast Cancer 97 0.351
11
VCC001 Vaccinia 49 0.348
12
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.346
13
P CLR023 Colorectal Cancer 99 0.340
14
P LNG032 Lung Cancer 98 0.337
15
P LVR013 Liver Disease 68 0.336
16
P LKM002 Leukemia 68 0.332
17
LVR012 Liver Cirrhosis 62 0.330
18
FCT001 Factor Viii Deficiency 51 0.327
19
P VNW001 Von Willebrand's Disease 65 0.315
20
HYP266 Hypoxia 57 0.307
21
P ADN016 Adenocarcinoma 64 0.304
22
P HPT023 Hepatocellular Carcinoma 100 0.302
23
HMN044 Human Immunodeficiency Virus Type 1 71 0.302
24
c HPT016 Hepatitis B 59 0.296
25
P OVR042 Ovarian Cancer 88 0.294
26
P CRN300 Coronary Heart Disease 1 63 0.293
27
ATM095 Autoimmune Disease 62 0.284
28
P GLM045 Glioma 63 0.283
29
DFC004 Deficiency Anemia 70 0.281
30
P VSC007 Vascular Disease 63 0.281
31
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.280
32
TXC005 Toxic Shock Syndrome 62 0.279
33
GLB015 Glioblastoma Multiforme 75 0.276
34
P DRR001 Diarrhea 55 0.276
35
GLL048 Glial Tumor 45 0.274
36
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.274
37
48X005 48,xyyy 39 0.272
38
P BLD134 Bladder Cancer 79 0.271
39
ATH013 Atherosclerosis Susceptibility 65 0.269
40
PRP030 Purpura 54 0.269
41
HLX001 Helix Syndrome 47 0.268
42
P HRP006 Herpes Simplex 65 0.267
43
ISC004 Ischemia 58 0.266
44
c PRC016 Pre-Eclampsia 63 0.265
45
P MYL006 Myeloid Leukemia 60 0.262
46
P GST053 Gastric Cancer 83 0.262
47
CYT002 Cytokine Deficiency 42 0.260
48
c HPT073 Hepatitis C Virus 72 0.260
49
IMM167 Immune Deficiency Disease 78 0.259
50
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.258
51
P BLD051 Blood Coagulation Disease 46 0.258
52
P INF032 Infertility 57 0.257
53
c SML038 Small Cell Cancer of the Lung 65 0.255
54
PLM033 Pulmonary Embolism 59 0.253
55
P PNC035 Pancreatic Cancer 84 0.253
56
P HRT032 Heart Disease 75 0.252
57
THY029 Thyroid Carcinoma 59 0.250
58
c SYS001 Systemic Lupus Erythematosus 86 0.248
59
c CHR684 Chronic Kidney Disease 70 0.247
60
P THR015 Thrombophilia 51 0.247
61
P MLN008 Melanoma 69 0.246
62
c HPT001 Hepatitis C 62 0.245
63
SQM006 Squamous Cell Carcinoma 60 0.244
64
c ACT075 Acute Myocardial Infarction 57 0.243
65
P PRS040 Prostate Cancer 97 0.242
66
P MYC007 Myocardial Infarction 70 0.240
67
P LYM118 Lymphoma 68 0.239
68
P MCR115 Microvascular Complications of Diabetes 5 66 0.239
69
SVR004 Severe Combined Immunodeficiency 73 0.239
70
MYL069 Myeloma, Multiple 85 0.238
71
FCT007 Factor Vii Deficiency 67 0.233
72
c LKM061 Leukemia, Acute Myeloid 84 0.230
73
ACQ007 Acquired Immunodeficiency Syndrome 60 0.230
74
CHL014 Cholera 59 0.229
75
ALL026 Allergic Hypersensitivity Disease 62 0.229
76
P LPS004 Lupus Erythematosus 61 0.225
77
P HYP086 Hypothyroidism 69 0.225
78
P DBT009 Diabetes Mellitus 64 0.223
79
IRN002 Iron Metabolism Disease 57 0.223
80
HYP056 Hypoglycemia 66 0.223
81
P NRB001 Neuroblastoma 72 0.222
82
CRB039 Cerebrovascular Disease 67 0.222
83
PRT037 Pertussis 65 0.221
84
c ACT071 Acute Kidney Failure 60 0.220
85
P LKM062 Leukemia, Acute Lymphoblastic 69 0.220
86
LNG099 Lung Disease 60 0.217
87
CNG034 Congestive Heart Failure 69 0.217
88
CRV035 Cervical Cancer 76 0.216
89
P PNM007 Pneumonia 68 0.215
90
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.214
91
STM007 Stomatitis 50 0.213
93
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.212
94
c HYP836 Hypercholesterolemia, Familial, 1 73 0.212
95
OST012 Osteoarthritis 78 0.211
96
P RHM011 Rheumatoid Arthritis 80 0.210
97
P GLM007 Glomerulonephritis 57 0.210
98
P PRD008 Periodontitis 64 0.208
99
47X002 47,xyy 49 0.206
100
P HPT021 Hepatitis 67 0.206
101
ADN018 Adenoma 59 0.205
102
BRN071 Brain Injury 49 0.204
103
P INF038 Influenza 68 0.204
104
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.201
105
MLR004 Malaria 81 0.200
106
c ACQ014 Acquired Hemophilia 45 0.199
107
CRH001 Crohn's Disease 74 0.199
108
HYP066 Hyperglycemia 61 0.198
109
LSH001 Leishmaniasis 63 0.198
110
P KLZ004 Kala-Azar 1 41 0.198
111
TRM010 Traumatic Brain Injury 51 0.197
112
c HPT003 Hepatitis a 62 0.196
113
OCL069 Ocular Motor Apraxia 51 0.195
114
PRT036 Peritonitis 64 0.193
115
c VRL010 Viral Hepatitis 52 0.193
116
P NPH012 Nephrotic Syndrome 60 0.193
117
P RHN004 Rhinitis 57 0.192
118
P OST002 Osteoporosis 74 0.191
119
FCT002 Factor Xi Deficiency 60 0.191
120
BNR002 Bone Resorption Disease 48 0.190
121
c ACT073 Acute Leukemia 58 0.190
122
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.189
123
P PSR002 Psoriasis 62 0.189
124
P EXN002 Exanthem 57 0.189
125
PST011 Pustulosis of Palm and Sole 52 0.188
126
P END044 Endometriosis 63 0.188
127
P RSP003 Respiratory Failure 74 0.188
128
SRC014 Sarcoma 65 0.187
129
P ECL001 Eclampsia 50 0.187
130
P GRF003 Graft-Versus-Host Disease 72 0.187
131
ESP021 Esophageal Cancer 90 0.187
132
CYS001 Cystic Fibrosis 81 0.185
133
P ALZ034 Alzheimer Disease 88 0.185
134
BCT022 Bacterial Infectious Disease 56 0.184
135
FTT001 Fatty Liver Disease 61 0.184
136
P ART023 Arthropathy 62 0.184
137
P FBR017 Fibrosarcoma 56 0.183
138
P ENC004 Encephalitis 61 0.183
139
P NRP001 Neuropathy 56 0.183
140
ULC004 Ulcerative Colitis 73 0.183
141
DPR016 Depression 63 0.182
142
SPN035 Spindle Cell Sarcoma 53 0.182
143
P CRD119 Cardiac Arrest 67 0.181
144
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.181
145
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.181
146
TTN003 Tetanus 65 0.181
147
DPH001 Diphtheria 60 0.180
148
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.180
149
SCH014 Schistosomiasis 57 0.180
150
P RCT021 Rectum Cancer 52 0.179
151
GST045 Gastroenteritis 59 0.179
152
END057 Endometrial Cancer 74 0.179
153
PRP027 Peripheral Vascular Disease 71 0.179
154
P KDN017 Kidney Cancer 60 0.178
155
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.178
156
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.178
157
SPN186 Spinal Cord Injury 60 0.178
158
DRM006 Dermatitis 61 0.177
159
P HYP098 Hypereosinophilic Syndrome 67 0.177
160
P NSP012 Nasopharyngeal Carcinoma 66 0.176
161
CLT003 Colitis 62 0.175
162
P BCL017 B-Cell Lymphoma 58 0.175
163
P LNG064 Lung Cancer Susceptibility 3 78 0.174
164
P ART022 Arthritis 69 0.174
165
P HMR003 Hemorrhagic Disease 53 0.174
166
c HYP595 Hypertension, Essential 84 0.174
167
P PNC044 Pancreatitis 61 0.174
168
P ART021 Arteriosclerosis 54 0.173
169
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.173
170
BRN024 Bronchitis 68 0.172
171
P VSC011 Vasculitis 62 0.171
172
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.171
173
ANG054 Angina Pectoris 66 0.170
174
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.170
175
MTH009 Mouth Disease 56 0.169
176
SKN016 Skin Disease 63 0.168
177
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.165
178
PPL022 Papilloma 54 0.165
179
P TRN020 Turner Syndrome 67 0.165
180
RBS001 Rabies 58 0.164
181
P CTR002 Cataract 60 0.164
182
P ENC018 Encephalopathy 61 0.164
183
c SVR001 Severe Acute Respiratory Syndrome 62 0.164
184
PLM001 Pulmonary Tuberculosis 69 0.163
185
P SYP003 Syphilis 58 0.163
186
ALC007 Alcohol Dependence 66 0.163
187
P DNG005 Dengue Virus 59 0.162
188
RTN017 Retinal Detachment 61 0.162
189
P PLM037 Pulmonary Hypertension 67 0.162
190
HDN002 Head Injury 46 0.162
191
c MLG068 Malignant Glioma 46 0.161
192
P AST007 Astrocytoma 51 0.161
193
P HYP750 Hypertriglyceridemia, Familial 62 0.161
194
P AMY004 Amyloidosis 70 0.160
195
P LPR021 Leprosy 3 69 0.160
196
FCT005 Factor Xiii Deficiency 52 0.159
197
HNS001 Hansen's Disease 34 0.159
198
GRN017 Granulocytopenia 44 0.159
199
INT007 Intermediate Coronary Syndrome 55 0.158
200
c SCL052 Scleroderma, Familial Progressive 61 0.158
201
P APL001 Aplastic Anemia 74 0.158
202
ANT024 Anthrax Disease 58 0.157
203
PPT005 Peptic Ulcer Disease 59 0.157
204
P SPP010 Suppressor of Tumorigenicity 3 51 0.157
205
LYM133 Lymphoma, Hodgkin, Classic 69 0.157
206
c DBT099 Diabetes Mellitus, Type I 65 0.156
207
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.156
208
TLN003 Telangiectasis 52 0.156
209
SPL018 Splenomegaly 48 0.156
210
GTR002 Goiter 53 0.155
211
SQM002 Squamous Cell Papilloma 46 0.155
212
MNT002 Mental Depression 58 0.155
213
PRS045 Prostatic Hypertrophy 53 0.155
215
P END033 Endocarditis 57 0.154
216
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.154
217
DYS073 Dysphagia 50 0.153
218
P TXP001 Toxoplasmosis 60 0.153
219
ANX010 Anxiety 73 0.153
220
P SKN015 Skin Carcinoma 66 0.153
221
P BRN019 Bernard-Soulier Syndrome 60 0.152
222
P THL005 Thalassemia 60 0.152
223
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.151
224
P LKM071 Leukemia, Chronic Lymphocytic 79 0.151
225
MST005 Mastitis 53 0.150
226
P DRM053 Dermatitis, Atopic 66 0.150
227
BRC012 Brucellosis 64 0.150
228
BCK006 Back Pain 42 0.150
229
P HYP076 Hyperthyroidism 55 0.149
230
P SCK005 Sickle Cell Disease 50 0.149
231
GRW007 Growth Hormone Deficiency 46 0.149
232
OVR094 Ovarian Epithelial Cancer 38 0.149
233
VRL011 Viral Infectious Disease 61 0.148
234
CVD001 Covid-19 44 0.148
235
TRN018 Transitional Cell Carcinoma 56 0.148
236
DNT012 Dental Caries 53 0.148
237
P ANT006 Antiphospholipid Syndrome 55 0.147
238
P CHR345 Chronic Pain 44 0.147
239
P MNN013 Meningitis 66 0.146
240
c ACT134 Acute Liver Failure 56 0.146
241
P HYD006 Hydrocephalus 66 0.146
242
URM002 Uremia 49 0.146
243
P BNG032 Benign Mesothelioma 46 0.146
244
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.145
245
THR004 Thrombocytosis 51 0.145
246
c LKM063 Leukemia, Chronic Myeloid 72 0.145
247
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.145
248
HMP009 Haemophilus Influenzae 43 0.144
249
P SZR006 Seizure Disorder 56 0.144
250
P HML002 Hemolytic Anemia 63 0.144
251
P MSC005 Muscular Dystrophy 66 0.144
252
SKN019 Skin Melanoma 68 0.143
253
ALL014 Allergic Encephalomyelitis 38 0.143
254
PRT013 Portal Hypertension 59 0.142
255
CHC001 Chickenpox 60 0.142
256
P INS002 in Situ Carcinoma 53 0.142
257
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.141
258
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.141
259
P PLY018 Polycythemia 56 0.141
260
ORL015 Oral Squamous Cell Carcinoma 43 0.141
261
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.140
262
RCK004 Rickets 68 0.140
263
ADL002 Adult Syndrome 70 0.140
264
ERY051 Erythroleukemia, Familial 56 0.140
265
VRC005 Varicose Veins 60 0.139
266
ORL011 Oral Cancer 60 0.139
267
P ANG015 Angioedema 57 0.139
268
LYM017 Lyme Disease 64 0.139
269
VSL002 Visual Epilepsy 59 0.138
270
PLM031 Poliomyelitis 64 0.138
271
P SCL018 Scoliosis 60 0.136
272
c SPN225 Spondyloarthropathy 1 73 0.136
273
THR035 Thrombasthenia 40 0.136
274
FCT003 Factor X Deficiency 54 0.136
275
P BND020 Bone Disease 59 0.136
276
P SYS005 Systemic Scleroderma 68 0.135
277
CHG001 Chagas Disease 66 0.134
278
c ACT135 Acute Graft Versus Host Disease 52 0.134
279
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.134
280
c MCR129 Microvascular Complications of Diabetes 1 66 0.134
281
c RHB024 Rhabdomyosarcoma 2 67 0.133
282
SFT003 Soft Tissue Sarcoma 56 0.133
283
P HDC001 Headache 57 0.133
284
RTN023 Retinitis 46 0.133
285
NRR001 Neuroretinitis 42 0.133
286
BRR014 Barrett Esophagus 65 0.131
287
OST003 Osteonecrosis 61 0.131
288
VTM033 Vitamin K Deficiency Bleeding 48 0.131
289
ANR007 Anorexia Nervosa 63 0.130
290
CRV045 Cervical Intraepithelial Neoplasia 39 0.130
291
c MCR112 Microvascular Complications of Diabetes 2 41 0.130
292
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.130
293
BLR008 Bilirubin Metabolic Disorder 57 0.130
294
MNN042 Meningioma, Radiation-Induced 62 0.129
295
PLG002 Plague 63 0.129
296
SYN007 Synovitis 54 0.128
297
c MNN043 Meningioma, Familial 74 0.128
298
P MJR001 Major Depressive Disorder 68 0.128
299
P URT039 Urticaria 58 0.128
300
SPN051 Spondylitis 51 0.128
301
P MYC008 Myocarditis 59 0.128
302
HMC014 Homocysteinemia 53 0.127
303
OTT002 Otitis Media 72 0.127
304
SPN021 Spinal Meningioma 50 0.127
305
THR016 Thrombophlebitis 51 0.127
306
P CND004 Candidiasis 58 0.127
307
c JVN010 Juvenile Rheumatoid Arthritis 64 0.127
308
CLN015 Colon Adenocarcinoma 65 0.126
309
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.126
310
P THY032 Thyroiditis 52 0.126
311
SCR001 Secretory Meningioma 41 0.126
312
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.126
313
EYD002 Eye Disease 58 0.125
314
IMP005 Impotence 52 0.125
315
c RRH015 Rare Hemorrhagic Disorder 23 0.125
316
P GLY013 Glycogen Storage Disease 60 0.125
317
PLC002 Plica Syndrome 36 0.125
318
MCL006 Macular Retinal Edema 55 0.124
319
INF009 Inflammatory Spondylopathy 31 0.123
320
P ATX030 Ataxia-Telangiectasia 82 0.123
321
TRN015 Transient Cerebral Ischemia 63 0.122
322
P DDN001 Duodenal Ulcer 52 0.122
323
IRN001 Iron Deficiency Anemia 59 0.122
324
P OVR082 Overgrowth Syndrome 50 0.122
325
CNS004 Constipation 58 0.122
326
CRB037 Cerebral Palsy 69 0.122
327
c HRD002 Hereditary Angioedema 60 0.121
328
HYP014 Hyperuricemia 52 0.121
329
P GLM040 Glioma Susceptibility 1 81 0.121
330
c ATR087 Atrial Standstill 1 75 0.121
331
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.121
332
ECH003 Echinococcosis 53 0.120
333
P RHB003 Rhabdomyosarcoma 63 0.120
334
PNC001 Pancytopenia 54 0.120
335
AGN016 Aging 56 0.120
336
TYP007 Typhoid Fever 63 0.119
337
CNN005 Connective Tissue Disease 68 0.119
338
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.119
339
P PYL005 Pyelonephritis 56 0.118
340
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.118
341
KRT009 Keratosis 51 0.118
342
ATX019 Ataxia with Vitamin E Deficiency 42 0.118
343
LYM019 Lymphosarcoma 46 0.117
344
P MYC084 Mycobacterium Tuberculosis 1 68 0.117
345
PNC129 Pancreatic Adenocarcinoma 68 0.116
346
c DNG003 Dengue Disease 59 0.116
347
NTR005 Nutritional Deficiency Disease 62 0.116
348
INF034 Infective Endocarditis 53 0.116
349
P SCH015 Schizophrenia 74 0.116
350
GST092 Gastroesophageal Reflux 67 0.116
351
PLY150 Polykaryocytosis Inducer 31 0.116
352
BRK010 Burkitt Lymphoma 67 0.116
353
P BPL003 Bipolar Disorder 56 0.116
354
c MJR024 Major Affective Disorder 9 41 0.114
355
c MJR022 Major Affective Disorder 8 38 0.114
356
P BRS044 Breast Adenocarcinoma 59 0.113
357
HRP004 Herpes Zoster 60 0.113
358
P MSC003 Muscular Atrophy 52 0.112
359
P MYP006 Myopia 55 0.112
360
MTB004 Metabolic Acidosis 50 0.112
361
PLY001 Polycythemia Vera 69 0.112
362
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.111
363
PRT011 Protein C Deficiency 44 0.111
364
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.110
365
P OPN001 Open-Angle Glaucoma 49 0.110
366
BRN004 Brain Edema 56 0.110
367
HMS001 Hemosiderosis 54 0.110
368
P MYP004 Myopathy 70 0.110
369
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.109
370
BRN056 Bronchopulmonary Dysplasia 57 0.109
371
ENT004 Enthesopathy 49 0.109
372
BRN002 Bronchiolitis 59 0.109
373
YLL002 Yellow Fever 61 0.109
374
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.109
375
HRW001 Hair Whorl 36 0.109
376
GST040 Gastric Adenocarcinoma 70 0.109
377
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.108
378
CHL068 Cholestasis 61 0.108
379
PNG002 Pain Agnosia 51 0.107
380
SCK003 Sickle Cell Anemia 74 0.107
381
P PLY019 Polyneuropathy 56 0.106
382
SML019 Smallpox 56 0.106
383
P EPL164 Epilepsy 71 0.106
384
DYS015 Dysentery 52 0.105
385
ATS010 Autosomal Recessive Disease 48 0.105
386
APP008 Appendicitis 61 0.104
387
CLF027 Cleft Palate, Isolated 64 0.104
388
P RRH023 Rare Hereditary Hemochromatosis 41 0.104
389
IGG001 Iga Glomerulonephritis 48 0.103
390
MDD018 Middle East Respiratory Syndrome 43 0.103
391
P NRF002 Neurofibromatosis 56 0.103
392
c PRD040 Periodontitis, Chronic 53 0.103
393
NSS002 Neisseria Meningitidis Infection 47 0.103
394
KHN001 Kuhnt-Junius Degeneration 47 0.102
395
HYD002 Hydronephrosis 60 0.102
396
CHR074 Choriocarcinoma 47 0.102
397
RFR010 Refractory Anemia 48 0.101
398
OST017 Osteomyelitis 64 0.101
399
c BRN108 Branchiootic Syndrome 1 62 0.101
400
BRN028 Brain Cancer 74 0.100
401
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.100
402
DGN001 Degenerative Disc Disease 48 0.100
403
c JVN061 Juvenile Arthritis 60 0.100
404
CTN007 Cutaneous Leishmaniasis 62 0.099
405
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.099
406
P CNJ013 Conjunctivitis 65 0.099
407
P MCR010 Microcephaly 59 0.099
408
c BTT014 Beta-Thalassemia 74 0.099
409
P CHN012 Chondrosarcoma 56 0.099
410
c NRF023 Neurofibromatosis, Type Ii 80 0.098
411
LMY002 Leiomyoma 52 0.098
412
ESP002 Esophageal Varix 51 0.097
413
P GCH001 Gaucher's Disease 63 0.097
414
P OPT006 Optic Nerve Disease 60 0.097
415
P MDL005 Medulloblastoma 77 0.097
416
GT001 Gout 64 0.097
417
P PRP029 Porphyria 62 0.097
418
P ADL017 Adult T-Cell Leukemia 56 0.097
419
CHR100 Chronic Ulcer of Skin 55 0.097
420
c WLM018 Wilms Tumor 5 61 0.096
421
VLV047 Volvulus of Midgut 49 0.096
422
THY030 Thyroid Gland Disease 52 0.096
423
P TRT010 Teratoma 52 0.096
424
c MST023 Mesothelioma, Malignant 57 0.096
425
CRD132 Cardiac Conduction Defect 58 0.096
426
P CLC063 Celiac Disease 1 66 0.096
427
VRL003 Variola Major 42 0.095
428
AMN001 Amenorrhea 54 0.095
429
HPT004 Hepatic Coma 45 0.093
430
P HYP083 Hypopituitarism 53 0.093
431
P HYP061 Hypertrophic Cardiomyopathy 70 0.093
432
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.093
433
RTN020 Retinal Vascular Disease 46 0.093
434
DMY004 Demyelinating Disease 52 0.093
435
c ACQ042 Acquired Hemophilia a 37 0.092
436
URL001 Urolithiasis 45 0.092
437
IDP070 Idiopathic Scoliosis 42 0.092
438
CLF001 Cleft Lip 53 0.092
439
EPD015 Epidemic Typhus 45 0.091
440
IRR002 Irritable Bowel Syndrome 65 0.090
441
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.090
442
P SML001 Small Cell Carcinoma 52 0.090
443
P ACT008 Actinic Keratosis 53 0.090
444
TCK001 Tick-Borne Encephalitis 56 0.089
445
P LRY044 Larynx Cancer 55 0.089
446
HMR002 Hemarthrosis 45 0.089
447
HMP018 Hemophilic Arthropathy 34 0.088
448
P SNS001 Sensorineural Hearing Loss 60 0.088
449
CHL079 Children's Interstitial Lung Disease 26 0.087
450
NRT004 Neuritis 52 0.087
451
PST092 Posttransplant Acute Limbic Encephalitis 29 0.087
452
P GLL018 Gallbladder Cancer 57 0.087
453
PLR007 Pleural Empyema 50 0.087
454
CHR005 Chorioamnionitis 51 0.086
455
ACN002 Acanthosis Nigricans 60 0.086
456
CRH005 Crohn's Colitis 53 0.086
457
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.086
458
CYN002 Cyanosis, Transient Neonatal 45 0.086
459
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.085
460
c GCH015 Gaucher Disease, Type I 70 0.085
461
P LMY004 Leiomyosarcoma 63 0.085
462
APH002 Aphasia 57 0.085
463
c HRD202 Hereditary Lymphedema I 50 0.085
464
P HYP265 Hypotonia 43 0.085
465
RHM001 Rheumatic Fever 60 0.084
466
ANX004 Anoxia 40 0.084
468
P TTR001 Tetralogy of Fallot 70 0.084
469
INT146 Intervertebral Disc Disease 63 0.084
470
PFF001 Pfeiffer Syndrome 79 0.084
471
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.083
472
BLD131 Bladder Urothelial Carcinoma 62 0.083
473
P RTN016 Retinal Degeneration 53 0.083
474
RYN005 Raynaud Phenomenon 47 0.083
475
RDC006 Red Cell Aplasia 43 0.083
476
KWS002 Kawasaki Disease 65 0.082
477
BDD001 Budd-Chiari Syndrome 63 0.082
478
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.082
479
P TRC086 Trichohepatoenteric Syndrome 1 62 0.082
480
BLD053 Blood Platelet Disease 49 0.082
481
MST004 Mast Cell Neoplasm 42 0.081
482
P PRR002 Pure Red-Cell Aplasia 47 0.081
483
SYN036 Syncope 45 0.080
484
P PTT006 Pituitary Adenoma 55 0.080
485
TRY001 Trypanosomiasis 50 0.080
486
LPR001 Lepromatous Leprosy 50 0.080
487
EXT007 Extracutaneous Mastocytoma 38 0.079
488
HMP001 Hemopericardium 48 0.079
489
c GRV008 Graves Disease 1 56 0.079
490
FBR047 Fibromyalgia 58 0.079
491
P INT068 Intestinal Disease 53 0.079
492
CRP001 Carpal Tunnel Syndrome 67 0.079
493
LST001 Listeriosis 56 0.078
494
NRL005 Neurilemmoma 60 0.078
495
THR013 Thoracic Outlet Syndrome 54 0.078
496
SPN019 Spondylolisthesis 51 0.078
497
P MMB011 Membranous Nephropathy 50 0.078
498
SPP011 Suppression of Tumorigenicity 12 59 0.078
499
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.078
500
c FNC043 Fanconi Anemia, Complementation Group E 62 0.078
501
LKP003 Leukoplakia 39 0.077
502
MNN009 Meningoencephalitis 49 0.077
503
CRC021 Carcinosarcoma 62 0.077
504
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.077
505
CMR002 Coumarin Resistance 56 0.076
506
P OLG002 Oligodendroglioma 67 0.076
507
c MTR002 Mitral Valve Insufficiency 48 0.076
508
CRT015 Carotid Artery Occlusion 45 0.076
509
MLD001 Melioidosis 68 0.076
510
c MLG079 Malignant Pleural Mesothelioma 42 0.076
511
P CLL015 Collagen Disease 47 0.076
512
P BRN022 Bronchiectasis 59 0.075
513
P FRG001 Fragile X Syndrome 70 0.075
514
P ANR048 Aniridia 1 63 0.075
515
P LCH002 Lichen Planus 53 0.075
516
NRM005 Neuromuscular Disease 64 0.075
517
QFV001 Q Fever 60 0.074
518
CRT072 Creutzfeldt-Jakob Disease 70 0.074
519
ONC002 Onchocerciasis 52 0.074
520
P MLT007 Multiple Epiphyseal Dysplasia 58 0.073
521
MCR004 Macroglobulinemia 49 0.073
522
CMP034 Complete Androgen Insensitivity Syndrome 46 0.072
523
CRD223 Cardiac Arrhythmia 60 0.072
524
GNG003 Gingival Recession 44 0.072
525
FML037 Female Breast Cancer 52 0.072
526
HMP005 Hemiplegia 55 0.072
527
ASP007 Aspiration Pneumonia 48 0.072
528
QDR001 Quadriplegia 48 0.071
529
HST010 Histiocytosis 48 0.071
530
P PLM034 Pulmonary Emphysema 55 0.070
531
SLC006 Silicosis 56 0.070
532
P DYS154 Dystonia 65 0.070
533
CNT047 Contact Dermatitis 58 0.070
534
DVR002 Diverticulitis 43 0.069
535
SNG003 Single Ventricular Heart 30 0.069
536
SPN027 Spinal Stenosis 59 0.069
537
P RRT020 Rare Tumor 41 0.069
538
P BNG030 Benign Ependymoma 60 0.069
539
P EHL001 Ehlers-Danlos Syndrome 58 0.069
540
FNG017 Fungal Infectious Disease 53 0.069
541
GRD007 Grade Iii Astrocytoma 59 0.069
542
CLL010 Cellular Ependymoma 54 0.068
543
IRD001 Iridocyclitis 53 0.068
544
P MVM001 Movement Disease 63 0.068
545
ATN004 Autonomic Neuropathy 45 0.068
546
RDN001 Reading Disorder 40 0.068
547
P PRD006 Prader-Willi Syndrome 59 0.068
548
SMN007 Seminoma 43 0.068
549
P SJG008 Sjogren Syndrome 61 0.067
550
c ANG068 Angioedema, Hereditary, Type I 57 0.067
551
P EPD016 Epidermolysis Bullosa 53 0.067
552
PLR008 Pleurisy 50 0.067
553
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.067
554
ACT064 Acute Necrotizing Encephalitis 33 0.067
555
P LCT001 Lactic Acidosis 51 0.066
556
BRT054 Brittle Bone Disorder 72 0.066
557
P ART018 Aortic Valve Insufficiency 49 0.066
558
c CHR682 Chronic Bilirubin Encephalopathy 39 0.066
559
c DPH024 Diaphragmatic Hernia, Congenital 63 0.066
560
TRC008 Trachoma 53 0.066
561
ATX010 Ataxia Neuropathy Spectrum 34 0.065
562
BLD137 Blood Group--Ahonen 16 0.065
563
NNT012 Neonatal Jaundice 53 0.065
564
ERY004 Erysipelas 49 0.065
565
MRF001 Marfan Syndrome 77 0.064
566
CLC006 Calcinosis 48 0.064
567
ANS011 Anus Cancer 56 0.064
568
END040 Endogenous Depression 55 0.063
569
THY111 Thyroid Carcinoma, Familial Medullary 67 0.063
570
THY125 Thyroid Gland Medullary Carcinoma 50 0.063
571
c INH004 Inherited Blood Coagulation Disease 30 0.063
572
49X006 49, Xxxxy Syndrome 41 0.063
573
c ACT004 Acute Diarrhea 39 0.063
574
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.063
575
c INH020 Inherited Metabolic Disorder 47 0.063
576
LYM021 Lymphadenitis 57 0.062
577
TNG007 Tongue Carcinoma 51 0.062
578
MMM001 Mammary Paget's Disease 53 0.062
579
c PRM196 Premature Ovarian Failure 1 67 0.062
580
c INF071 Inflammatory Bowel Disease 1 67 0.061
581
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.060
582
P FBR003 Fibrous Histiocytoma 44 0.060
583
PRT129 Prothrombin Deficiency, Congenital 50 0.060
584
P ANG001 Angelman Syndrome 69 0.059
585
BLR001 Biliary Atresia 50 0.059
586
c VNW005 Von Willebrand Disease, Type 1 48 0.059
587
c ADN012 Adenocarcinoma in Situ 42 0.059
588
HPR006 Heparin Cofactor Ii Deficiency 40 0.059
589
P OPT009 Optic Neuritis 57 0.059
590
CGL001 Coagulation Protein Disease 10 0.059
591
ORL012 Oral Leukoplakia 39 0.059
592
PRC002 Paracoccidioidomycosis 54 0.058
593
P KRT007 Keratoconus 50 0.058
594
ACS001 Acoustic Neuroma 56 0.058
595
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.058
596
APP009 Appendix Adenocarcinoma 44 0.058
597
INT051 Intussusception 53 0.057
598
GLS018 Glass Syndrome 57 0.057
599
P MLT074 Multiple Endocrine Neoplasia 56 0.057
600
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.056
601
MCN001 Mucinous Adenocarcinoma 49 0.056
602
INT067 Interstitial Nephritis 48 0.056
603
c CHR418 Chronic Leukemia 49 0.055
604
ADR016 Adrenal Cortical Carcinoma 48 0.055
605
URT001 Urethritis 49 0.055
606
P AXN002 Axenfeld-Rieger Syndrome 59 0.055
607
AND002 Androgen Insensitivity Syndrome 66 0.054
608
CRY014 Cryptococcal Meningitis 48 0.054
609
c HNT011 Huntington Disease-Like 3 38 0.054
610
PNM005 Pneumonic Plague 51 0.054
611
FCL012 Facial Paralysis 46 0.053
612
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.053
613
OVR059 Ovary Adenocarcinoma 53 0.053
614
SGN002 Signet Ring Cell Adenocarcinoma 45 0.053
615
CRV040 Cervix Carcinoma 51 0.053
616
BLL003 Bell's Palsy 51 0.052
617
P MLG056 Malignant Hyperthermia 67 0.052
618
BRN014 Bronchopneumonia 54 0.052
619
GRM010 Germ Cells Tumors 34 0.051
620
PTH003 Pathologic Nystagmus 52 0.051
621
P OTS001 Otosclerosis 49 0.051
622
P PRP003 Porphyria Cutanea Tarda 67 0.051
623
CRT017 Cartilage Disease 54 0.050
624
OCC006 Occipital Horn Syndrome 60 0.050
625
LNG108 Langerhans Cell Histiocytosis 58 0.050
626
PRS042 Prostate Disease 43 0.050
627
ALR002 Al-Raqad Syndrome 33 0.050
628
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.049
629
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.049
630
c NRF024 Neurofibromatosis, Type I 77 0.048
631
HNT002 Hantavirus Pulmonary Syndrome 50 0.048
632
NRM004 Neuroma 51 0.048
633
ANC001 Ancylostomiasis 43 0.047
634
SKN013 Skin Benign Neoplasm 51 0.047
635
c PSD048 Pseudo-Von Willebrand Disease 39 0.047
636
TNS007 Taeniasis 45 0.047
637
c ACT078 Acute Porphyria 51 0.046
638
NSP002 Nasopharyngitis 43 0.046
639
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.046
640
c CNG415 Congenital Disorder of Glycosylation, Type Ia 55 0.046
641
VNH007 Von Hippel-Lindau Syndrome 73 0.046
642
CLR003 Clear Cell Adenocarcinoma 50 0.046
643
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.046
644
P HRD011 Hereditary Spherocytosis 60 0.046
645
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.046
646
ART001 Arterial Tortuosity Syndrome 66 0.045
647
FTL012 Fetal and Neonatal Alloimmune Thrombocytopenia 44 0.045
648
c LTN004 Late-Onset Retinal Degeneration 59 0.044
649
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 30 0.044
650
TXC002 Toxic Encephalopathy 53 0.044
651
CLB002 Clubfoot 51 0.044
652
ZKF001 Zika Fever 47 0.044
653
PRM013 Premature Menopause 41 0.044
654
SLD003 Sialadenitis 49 0.043
655
P ALP106 Alport Syndrome 1, X-Linked 55 0.043
656
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.043
657
BBN001 Bubonic Plague 41 0.043
658
ANP009 Anaplastic Oligodendroglioma 43 0.043
659
P PLT029 Platelet Groups--Ko System 16 0.043
660
P PRT026 Parotitis 42 0.042
661
URN003 Urinary Schistosomiasis 46 0.042
662
GNR003 Generalized Atherosclerosis 46 0.042
663
P RNL007 Renal Tubular Acidosis 51 0.041
664
P ALP004 Alport Syndrome 68 0.041
665
CLB010 Coloboma of Macula 52 0.041
666
P TST021 Testicular Germ Cell Tumor 60 0.041
667
HYD005 Hydrocele 46 0.041
668
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.041
669
P END039 Endodermal Sinus Tumor 44 0.041
670
BRR002 Barrett's Adenocarcinoma 36 0.040
671
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.040
672
JVN009 Juvenile Pilocytic Astrocytoma 55 0.040
673
P SHR029 Short Syndrome 63 0.039
674
CLL002 Collecting Duct Carcinoma 53 0.039
675
c RTN041 Retinitis Pigmentosa 11 42 0.038
676
BLD052 Blood Group Incompatibility 32 0.037
677
TST018 Testicular Yolk Sac Tumor 39 0.037
678
FBR002 Fibrosarcoma of Bone 34 0.037
679
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.036
680
MNN017 Mononeuropathy 42 0.036
681
VLC001 Velocardiofacial Syndrome 54 0.035
682
ALT002 Aleutian Mink Disease 28 0.035
684
P INN002 Inner Ear Disease 47 0.034
685
AML001 Amelanotic Melanoma 39 0.034
686
c GLY060 Glycogen Storage Disease Ia 63 0.030
687
XLN228 X-Linked Recessive Disease 26 0.029
Content
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