Search results for Menadione

524 hits were found for Menadione

# Family MCID Name MIFTS Score
1
P PNC035 Pancreatic Cancer 87 0.049
2
P EXN002 Exanthem 57 0.049
3
P SKN013 Skin Benign Neoplasm 43 0.049
4
END072 Endotheliitis 42 0.049
5
AYM001 Ayme-Gripp Syndrome 41 0.049
6
P CLR023 Colorectal Cancer 97 0.040
7
P LNG032 Lung Cancer 95 0.040
8
P ADN016 Adenocarcinoma 69 0.040
9
P HPT021 Hepatitis 69 0.040
10
MLN008 Melanoma 62 0.040
11
P PNC044 Pancreatitis 61 0.040
12
ORL011 Oral Cancer 56 0.040
13
HYP266 Hypoxia 56 0.040
14
c CLR085 Colorectal Cancer 1 45 0.040
15
FXF002 Fox-Fordyce Disease 36 0.040
16
c PNC095 Pancreatic Cancer 3 30 0.040
17
c CLR079 Colorectal Cancer 2 29 0.040
18
c CLR075 Colorectal Cancer 3 28 0.040
19
c PNC111 Pancreatic Cancer 2 28 0.040
20
c PNC094 Pancreatic Cancer 1 27 0.040
21
RDC011 Reducing Body Myopathy, X-Linked 1a, Severe, Infantile or Early Childhood Onset 19 0.040
22
RDC012 Reducing Body Myopathy, X-Linked 1b, with Late Childhood or Adult Onset 13 0.040
23
P ALZ034 Alzheimer Disease 92 0.028
24
P HPT023 Hepatocellular Carcinoma 92 0.028
25
P PRS040 Prostate Cancer 90 0.028
26
P RHM011 Rheumatoid Arthritis 89 0.028
27
P OST012 Osteoarthritis 83 0.028
28
MLR004 Malaria 83 0.028
29
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.028
30
P HNT016 Huntington Disease 80 0.028
31
P PLM037 Pulmonary Hypertension 79 0.028
32
P MYC007 Myocardial Infarction 79 0.028
33
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.028
34
P MDL005 Medulloblastoma 77 0.028
35
P ART022 Arthritis 75 0.028
36
P LVR013 Liver Disease 75 0.028
37
P HRT032 Heart Disease 75 0.028
38
STR067 Stroke, Ischemic 75 0.028
39
CRH001 Crohn's Disease 75 0.028
40
INS024 Insulin-Like Growth Factor I 75 0.028
41
P CRN211 Coronary Artery Disease 74 0.028
42
c HPT073 Hepatitis C Virus 73 0.028
43
WLS001 Wilson Disease 72 0.028
44
CNG034 Congestive Heart Failure 72 0.028
45
P LKM002 Leukemia 71 0.028
46
SCK003 Sickle Cell Anemia 71 0.028
47
P NRB001 Neuroblastoma 70 0.028
48
KWS002 Kawasaki Disease 70 0.028
49
TST021 Testicular Germ Cell Tumor 69 0.028
50
c HYP595 Hypertension, Essential 69 0.028
51
PRP027 Peripheral Vascular Disease 68 0.028
52
c HPT001 Hepatitis C 68 0.028
53
P GLB002 Glioblastoma 68 0.028
54
P CRD011 Cardiomyopathy 68 0.028
55
ISC006 Ischemic Heart Disease 68 0.028
56
PCK002 Pick Disease 68 0.028
57
P PNM007 Pneumonia 68 0.028
58
ANX002 Anxiety Disorder 67 0.028
59
WRN001 Werner Syndrome 67 0.028
60
LVR012 Liver Cirrhosis 67 0.028
61
P MYP004 Myopathy 67 0.028
62
VSC007 Vascular Disease 67 0.028
63
EWN003 Ewing Sarcoma 66 0.028
64
P ATR011 Atrial Fibrillation 66 0.028
65
P KDN018 Kidney Disease 66 0.028
66
c CHR089 Chronic Kidney Failure 66 0.028
67
SKN016 Skin Disease 66 0.028
68
BRC012 Brucellosis 66 0.028
69
DWN001 Down Syndrome 66 0.028
70
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.028
71
ATH003 Atherosclerosis 65 0.028
72
DMN002 Dementia 65 0.028
73
CNT098 Central Core Disease 65 0.028
74
P AST007 Astrocytoma 65 0.028
75
c HPT016 Hepatitis B 64 0.028
76
P ART023 Arthropathy 64 0.028
77
P ORT004 Orthostatic Intolerance 64 0.028
78
HMT002 Hematologic Cancer 64 0.028
79
DFC004 Deficiency Anemia 64 0.028
80
P THR014 Thrombocytopenia 64 0.028
81
LNG099 Lung Disease 64 0.028
82
P OST002 Osteoporosis 64 0.028
83
P INF037 Inflammatory Bowel Disease 63 0.028
84
CRB039 Cerebrovascular Disease 63 0.028
85
P ALX003 Alexander Disease 63 0.028
86
GLB015 Glioblastoma Multiforme 63 0.028
87
P ENC004 Encephalitis 63 0.028
88
c HMP004 Hemophilia B 62 0.028
89
P HML002 Hemolytic Anemia 62 0.028
90
CNN005 Connective Tissue Disease 62 0.028
91
GST092 Gastroesophageal Reflux 62 0.028
92
APH001 Aphthous Stomatitis 62 0.028
93
ACN011 Acne 62 0.028
94
FCT003 Factor X Deficiency 61 0.028
95
ISC004 Ischemia 61 0.028
96
P TXP001 Toxoplasmosis 61 0.028
97
P PSR002 Psoriasis 61 0.028
98
CRD119 Cardiac Arrest 61 0.028
99
FCT007 Factor Vii Deficiency 61 0.028
100
HYP066 Hyperglycemia 61 0.028
101
MTH009 Mouth Disease 61 0.028
102
P RCK004 Rickets 61 0.028
103
c ACT075 Acute Myocardial Infarction 60 0.028
104
ACQ007 Acquired Immunodeficiency Syndrome 60 0.028
105
P INT068 Intestinal Disease 60 0.028
106
PLM033 Pulmonary Embolism 60 0.028
107
P GLM045 Glioma 60 0.028
108
P NRV006 Nervous System Cancer 60 0.028
109
P GST049 Gastrointestinal System Cancer 60 0.028
110
PRM097 Primary Immunodeficiency Disease 60 0.028
111
c VRL010 Viral Hepatitis 60 0.028
112
WLL001 Williams-Beuren Syndrome 60 0.028
113
P DRR001 Diarrhea 60 0.028
114
RBR001 Roberts Syndrome 60 0.028
115
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.028
116
c CNT035 Central Nervous System Disease 60 0.028
117
P ORL007 Oral Cavity Cancer 59 0.028
118
c HPT003 Hepatitis a 59 0.028
119
P THR015 Thrombophilia 59 0.028
120
GST045 Gastroenteritis 59 0.028
121
P ENC018 Encephalopathy 59 0.028
122
P INF032 Infertility 59 0.028
123
WLL006 Wells Syndrome 59 0.028
124
LPD008 Lipid Metabolism Disorder 58 0.028
125
c FML001 Familial Atrial Fibrillation 58 0.028
126
P SHR029 Short Syndrome 58 0.028
127
ART021 Arteriosclerosis 58 0.028
128
P HYP060 Hyperinsulinism 58 0.028
129
ETN001 Eating Disorder 58 0.028
130
P CTR002 Cataract 58 0.028
131
RHM027 Rheumatic Disease 58 0.028
132
P MTR012 Mitral Valve Disease 58 0.028
133
P HYP069 Hyperparathyroidism 58 0.028
134
P MSC007 Muscle Hypertrophy 58 0.028
135
PNC034 Pancreas Disease 58 0.028
136
BNC003 Bone Cancer 58 0.028
137
CHL071 Child Syndrome 58 0.028
138
c PNC108 Pancreatitis, Hereditary 58 0.028
139
P HMP007 Hemophilia 57 0.028
140
KND001 Kindler Syndrome 57 0.028
141
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.028
142
CTS003 Coats Disease 57 0.028
143
EMB004 Embryonal Carcinoma 57 0.028
144
ART017 Aortic Disease 57 0.028
145
CHY002 Chylomicron Retention Disease 57 0.028
146
THR024 Thrombosis 57 0.028
147
CRT016 Carotid Artery Disease 57 0.028
148
P HMR003 Hemorrhagic Disease 57 0.028
149
ANR040 Aneurysm 57 0.028
150
WST001 West Syndrome 57 0.028
151
P INT143 Interstitial Cystitis 57 0.028
152
P SZR006 Seizure Disorder 56 0.028
153
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.028
154
TRN015 Transient Cerebral Ischemia 56 0.028
155
NRN004 Neuroendocrine Tumor 56 0.028
156
c HYP615 Hyperparathyroidism, Familial Primary 56 0.028
157
P WVR001 Weaver Syndrome 56 0.028
158
P ANT006 Antiphospholipid Syndrome 56 0.028
159
GST050 Gastrointestinal System Disease 56 0.028
160
VRL011 Viral Infectious Disease 55 0.028
161
ART111 Artery Disease 55 0.028
162
JNT002 Joint Disorders 55 0.028
163
PRP019 Peripheral Nervous System Disease 55 0.028
164
CCC001 Coccidioidomycosis 55 0.028
165
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.028
166
GLC003 Glucose Intolerance 55 0.028
167
MLN007 Male Infertility 55 0.028
168
GLS001 Gliosarcoma 55 0.028
169
HPT022 Hepatoblastoma 55 0.028
170
END030 End Stage Renal Failure 55 0.028
171
PLS007 Plasmodium Falciparum Malaria 55 0.028
172
EXT034 Extrinsic Allergic Alveolitis 54 0.028
173
c THR092 Thrombophilia Due to Thrombin Defect 54 0.028
174
RCT018 Rectal Neoplasm 54 0.028
175
c PND001 Pain Disorder 54 0.028
176
c VRL007 Viral Encephalitis 54 0.028
177
RHM001 Rheumatic Fever 54 0.028
178
c HPT007 Hepatitis E 54 0.028
179
NWC001 Newcastle Disease 54 0.028
180
PLN006 Poland Syndrome 54 0.028
181
CND002 Conduct Disorder 54 0.028
182
P INT030 Intracranial Aneurysm 54 0.028
183
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.028
184
P VNS003 Venous Insufficiency 54 0.028
185
c ART101 Aortic Valve Disease 2 53 0.028
186
P MTC069 Mitochondrial Disorders 53 0.028
187
C3D001 C3 Deficiency 53 0.028
188
DMY004 Demyelinating Disease 53 0.028
189
KDS001 Kid Syndrome 53 0.028
190
FDL002 Food Allergy 53 0.028
191
PRT014 Protein S Deficiency 53 0.028
192
SLP005 Sleep Disorder 53 0.028
193
OLV001 Olivopontocerebellar Atrophy 53 0.028
194
HMR039 Hemorrhage, Intracerebral 53 0.028
195
ADL002 Adult Syndrome 52 0.028
196
TTH006 Tooth Disease 52 0.028
197
BRN106 Burns 52 0.028
198
KRT002 Keratomalacia 52 0.028
199
TRM010 Traumatic Brain Injury 52 0.028
200
PRT058 Pure Autonomic Failure 52 0.028
201
HMG005 Hemoglobinopathy 52 0.028
202
ALL026 Allergic Hypersensitivity Disease 52 0.028
203
P MSC033 Muscle Disorders 52 0.028
204
PRT011 Protein C Deficiency 52 0.028
205
DGN001 Degenerative Disc Disease 52 0.028
206
P SPS003 Spastic Diplegia 52 0.028
207
BRN071 Brain Injury 52 0.028
208
MYC002 Mycobacterium Avium Complex Disease 52 0.028
209
PRS042 Prostate Disease 52 0.028
210
IRN001 Iron Deficiency Anemia 52 0.028
211
CRC006 Carcinoid Syndrome 52 0.028
212
c INF071 Inflammatory Bowel Disease 1 51 0.028
213
VSC006 Vascular Cancer 51 0.028
214
GNR004 Generalized Anxiety Disorder 51 0.028
215
P HRD018 Hair Disease 51 0.028
216
HYP005 Hypokalemia 51 0.028
217
ATR060 Atrial Standstill, Digenic 51 0.028
218
IMM136 Immune System Disease 51 0.028
219
CRS005 Crest Syndrome 51 0.028
220
SCK005 Sickle Cell Disease 51 0.028
221
CLN019 Colonic Disease 51 0.028
222
CCC002 Coccidiosis 51 0.028
223
CRN030 Coronary Stenosis 51 0.028
224
PLG002 Plague 51 0.028
225
SCH002 Schnitzler Syndrome 51 0.028
226
STM006 Stomach Disease 50 0.028
227
c ART115 Aortic Valve Disease 1 50 0.028
228
GRD007 Grade Iii Astrocytoma 50 0.028
229
INT007 Intermediate Coronary Syndrome 50 0.028
230
CLN015 Colon Adenocarcinoma 50 0.028
231
CLC006 Calcinosis 50 0.028
232
BNF002 Bone Fracture 50 0.028
233
c ACT068 Acute Cystitis 50 0.028
234
URN009 Urinary System Disease 50 0.028
235
P CLL015 Collagen Disease 50 0.028
236
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.028
237
RHM028 Rheumatic Heart Disease 50 0.028
238
PNM001 Pneumocystosis 50 0.028
239
DRG003 Drug Dependence 50 0.028
240
CSY001 C Syndrome 50 0.028
241
HYP037 Hyperhomocysteinemia 50 0.028
242
OVR063 Overnutrition 50 0.028
243
HYP006 Hypertensive Heart Disease 50 0.028
244
P URF003 Urofacial Syndrome 1 50 0.028
245
LPD009 Lipid Storage Disease 49 0.028
246
GLM004 Gliomatosis Cerebri 49 0.028
247
LRN003 Learning Disability 49 0.028
248
c ACT071 Acute Kidney Failure 49 0.028
249
PRN021 Paranasal Sinus Disease 49 0.028
250
c INH020 Inherited Metabolic Disorder 49 0.028
251
BCL002 B Cell Deficiency 49 0.028
252
c DWL002 Dowling-Degos Disease 1 49 0.028
253
ATN005 Autonomic Dysfunction 49 0.028
254
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.028
255
LMB062 Limb Ischemia 48 0.028
256
LPD004 Lipoid Nephrosis 48 0.028
257
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.028
258
P FML035 Familial Hyperlipidemia 48 0.028
259
ACT017 Acute Chest Syndrome 48 0.028
260
QBC001 Quebec Platelet Disorder 48 0.028
261
PLS009 Plasma Cell Neoplasm 48 0.028
262
CRN017 Coronary Thrombosis 48 0.028
263
ATN002 Autonomic Nervous System Disease 48 0.028
264
P TRC086 Trichohepatoenteric Syndrome 1 48 0.028
265
P RNL015 Renal Hypertension 48 0.028
266
c CNG027 Congenital Hemolytic Anemia 48 0.028
267
c HMG001 Hemoglobin C Disease 47 0.028
268
SBS004 Substance Dependence 47 0.028
269
VND001 Vein Disease 47 0.028
270
PRT030 Parathyroid Gland Disease 47 0.028
271
PRN014 Paronychia 47 0.028
272
INT253 Intestinal Benign Neoplasm 47 0.028
273
MLK006 Milk Allergy 47 0.028
274
SDD007 Sudden Cardiac Death 47 0.028
275
AMN002 Amino Acid Metabolic Disorder 47 0.028
276
BRD001 Brody Myopathy 47 0.028
277
PST095 Post-Thrombotic Syndrome 47 0.028
278
UPP004 Upper Respiratory Tract Disease 46 0.028
279
CRB085 Cerebral Hemorrhage 46 0.028
280
PRP021 Peripheral Nervous System Neoplasm 46 0.028
281
HRT007 Heart Cancer 46 0.028
282
FLL008 Folliculitis 46 0.028
283
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.028
284
BLD053 Blood Platelet Disease 46 0.028
285
GLT021 Glutaricaciduria, Type I 46 0.028
286
CLC001 Calciphylaxis 46 0.028
287
SCR002 Scurvy 46 0.028
288
INC022 Inclusion-Cell Disease 46 0.028
289
CRB004 Cerebral Artery Occlusion 45 0.028
290
ACR041 Acromelic Frontonasal Dysostosis 45 0.028
291
P PLM025 Pulmonary Venoocclusive Disease 45 0.028
292
CRT017 Cartilage Disease 45 0.028
293
TCL003 T Cell Deficiency 45 0.028
294
HDN002 Head Injury 45 0.028
295
VSC047 Vascular Malformation 45 0.028
296
ACD009 Acid-Labile Subunit, Deficiency of 45 0.028
297
ALN001 Aland Island Eye Disease 45 0.028
298
VTM002 Vitamin B12 Deficiency 44 0.028
299
GDS001 Good Syndrome 44 0.028
300
CRD118 Cardiovascular Cancer 44 0.028
301
c MTR002 Mitral Valve Insufficiency 44 0.028
302
BNN003 Bone Inflammation Disease 44 0.028
303
SKN023 Skin Tag 44 0.028
304
P DYS021 Dysautonomia 44 0.028
305
c CHR431 Chronic Venous Insufficiency 44 0.028
306
c HMG003 Hemoglobin E Disease 44 0.028
307
PHY002 Physical Disorder 43 0.028
308
CRT015 Carotid Artery Occlusion 43 0.028
309
c SVR056 Severe Hemophilia a 43 0.028
310
BRT030 Birth Defects 43 0.028
311
RNL097 Renal Artery Disease 43 0.028
312
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.028
313
SKN027 Skin Conditions 43 0.028
314
MLR006 Male Reproductive Organ Cancer 43 0.028
315
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.028
316
EXC002 Exocrine Pancreatic Insufficiency 43 0.028
317
ACT058 Active Peptic Ulcer Disease 43 0.028
318
LKC003 Leukocyte Disease 43 0.028
319
SNS023 Sensory System Cancer 43 0.028
320
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.028
321
PRD004 Prediabetes Syndrome 43 0.028
322
P CRD132 Cardiac Conduction Defect 43 0.028
323
CRB008 Cerebral Atherosclerosis 43 0.028
324
P PLM040 Pulmonary Valve Disease 43 0.028
325
BHR001 Behr Syndrome 42 0.028
326
GLC008 Glucose Metabolism Disease 42 0.028
327
CRN025 Corneal Dystrophy 42 0.028
328
SXL003 Sexual Disorder 42 0.028
329
P BLD051 Blood Coagulation Disease 42 0.028
330
c VRL005 Viral Pneumonia 42 0.028
331
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.028
332
PRD011 Proud Syndrome 42 0.028
333
RBF001 Riboflavin Deficiency 42 0.028
334
c LNG031 Lung Benign Neoplasm 41 0.028
335
VNT011 Ventricular Fibrillation, Familial, 1 41 0.028
336
IRN002 Iron Metabolism Disease 41 0.028
337
PRM025 Primary Bacterial Infectious Disease 41 0.028
338
BRN080 Brain Ischemia 41 0.028
339
BRB001 Beriberi 41 0.028
340
OPP002 Opportunistic Mycosis 41 0.028
341
RPR002 Reproductive System Disease 41 0.028
342
CHR413 Chronic Myocardial Ischemia 41 0.028
343
CNV002 Conversion Disorder 41 0.028
344
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.028
345
PRS036 Parasitic Protozoa Infectious Disease 41 0.028
346
CLV009 Clove Syndrome, Somatic 41 0.028
347
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.028
348
STT004 Steatorrhea 40 0.028
349
CRT004 Carotid Artery Thrombosis 40 0.028
350
CWM001 Cow Milk Allergy 40 0.028
351
HRT012 Heart Valve Disease 40 0.028
352
ANG016 Angiokeratoma 40 0.028
353
RCT017 Rectal Disease 40 0.028
354
c CHR096 Chronic Pulmonary Heart Disease 40 0.028
355
ATX003 Ataxia with Isolated Vitamin E Deficiency 40 0.028
356
BND014 Bone Development Disease 40 0.028
357
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.028
358
c INF087 Inflammatory Bowel Disease 4 40 0.028
359
c PRM225 Primary Thrombocytopenia 39 0.028
360
c ACT004 Acute Diarrhea 39 0.028
361
P ART018 Aortic Valve Insufficiency 39 0.028
362
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.028
363
ACT088 Acute Insulin Response 39 0.028
364
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.028
365
CRB070 Cerebral Folate Deficiency 39 0.028
366
MNR003 Mineral Metabolism Disease 38 0.028
367
NSL022 Nasal Cavity Disease 38 0.028
368
PHS001 Phosphorus Metabolism Disease 38 0.028
369
HYP034 Hypertensive Encephalopathy 38 0.028
370
ADJ001 Adjustment Disorder 38 0.028
371
SPC003 Specific Developmental Disorder 38 0.028
372
MLG088 Malignant Germ Cell Tumor 38 0.028
373
c OST112 Osteoarthritis-5 38 0.028
374
DRG001 Drug Psychosis 38 0.028
375
c PRS116 Prostate Cancer 1 37 0.028
376
BNR001 Bone Remodeling Disease 37 0.028
377
c PSR017 Psoriasis 2 37 0.028
378
BLD054 Blood Protein Disease 37 0.028
379
WTH001 Withdrawal Disorder 37 0.028
380
PRP080 Peripheral Artery Disease 37 0.028
381
c PNC106 Pancreatic Agenesis 1 37 0.028
382
FNC002 Functional Diarrhea 37 0.028
383
BNS002 Bone Structure Disease 37 0.028
384
MDY003 Mody, Type Ii 36 0.028
385
NSY001 N Syndrome 36 0.028
386
ISC005 Ischemic Bone Disease 36 0.028
387
SCH072 Scheuermann Disease 36 0.028
388
PST055 Postural Hypotension 36 0.028
389
CRT013 Carotid Stenosis 36 0.028
390
GRM001 Germ Cell and Embryonal Cancer 36 0.028
391
NTR005 Nutritional Deficiency Disease 36 0.028
392
INT078 Intracranial Thrombosis 36 0.028
393
PYR016 Pyridoxine Deficiency 36 0.028
394
ALR002 Al-Raqad Syndrome 36 0.028
395
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.028
396
c THR037 Thrombocytopenia 2 35 0.028
397
SBS006 Sebastian Syndrome 35 0.028
398
IMM078 Immunodeficiency 21 35 0.028
399
ADL053 Adult Astrocytic Tumour 35 0.028
400
PHT003 Phototoxic Dermatitis 35 0.028
401
PNC028 Pancreatic Steatorrhea 34 0.028
402
MSC004 Muscle Tissue Disease 34 0.028
403
RDN001 Reading Disorder 34 0.028
404
BTN004 Biotin Deficiency 34 0.028
405
IMP003 Impaired Renal Function Disease 34 0.028
406
FLC001 Folic Acid Deficiency Anemia 34 0.028
407
MLR007 Male Reproductive System Disease 34 0.028
408
INT084 Intrinsic Cardiomyopathy 34 0.028
409
ANG049 Angioedema Induced by Ace Inhibitors 34 0.028
410
PLS010 Plasma Protein Metabolism Disease 34 0.028
411
CND006 Candida Glabrata 34 0.028
412
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 0.028
413
ACR002 Acrocapitofemoral Dysplasia 33 0.028
414
c HYP311 Hyperparathyroidism 3 33 0.028
415
SWL001 Swallowing Disorders 33 0.028
416
LNS003 Lens Disease 33 0.028
417
DDN007 Duodenal Disease 33 0.028
418
c CLR080 Colorectal Cancer 5 32 0.028
419
P HRT017 Heart Tumor 32 0.028
420
c ALZ043 Alzheimer's Disease 15 32 0.028
421
INT010 Intracranial Embolism 32 0.028
422
c SVR057 Severe Hemophilia B 32 0.028
423
c PLM130 Pulmonary Venoocclusive Disease 1 32 0.028
424
SPR035 Superior Vena Cava Syndrome 31 0.028
425
P ACT080 Acute Pulmonary Heart Disease 31 0.028
426
c NRV012 Nervous System Benign Neoplasm 31 0.028
427
c DRR007 Diarrhea 7 31 0.028
428
c HMG004 Hemoglobin D Disease 31 0.028
429
c GLB007 Glioblastoma 3 31 0.028
430
RNL001 Renal Artery Obstruction 31 0.028
431
IRS003 Iris Disease 31 0.028
432
HNS001 Hansen's Disease 30 0.028
433
VSC008 Vascular Hemostatic Disease 30 0.028
434
IMM068 Immunodeficiency 8 30 0.028
435
VTM003 Vitamin Metabolic Disorder 30 0.028
436
c PLM132 Pulmonary Venoocclusive Disease 2 30 0.028
437
MRG013 Mirage Syndrome 29 0.028
438
ATM016 Autoimmune Disease of Skin and Connective Tissue 29 0.028
439
c CLR077 Colorectal Cancer 10 29 0.028
440
c DRR009 Diarrhea 6 29 0.028
441
c TRC078 Trichohepatoenteric Syndrome 2 29 0.028
442
PRM243 Primary Bone Cancer 29 0.028
443
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.028
444
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.028
445
LPD027 Lip Disease 28 0.028
446
WRF003 Warfarin Syndrome 28 0.028
447
c MYC058 Myocardial Infarction 2 28 0.028
448
c ATR038 Atrial Fibrillation, Familial, 3 27 0.028
449
CRB031 Cerebral Arterial Disease 27 0.028
450
c ALZ014 Alzheimer Disease 16 27 0.028
451
IMM062 Immunodeficiency 11 26 0.028
452
c ATR039 Atrial Fibrillation, Familial, 4 26 0.028
453
c ATR069 Atrial Fibrillation, Familial, 12 25 0.028
454
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.028
455
c ATM007 Autoimmune Disease of Central Nervous System 25 0.028
456
RSP004 Respiratory System Benign Neoplasm 25 0.028
457
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.028
458
ATM052 Autoimmune Disease 1 25 0.028
459
c ATR035 Atrial Fibrillation, Familial, 6 25 0.028
460
c CLR083 Colorectal Cancer 8 24 0.028
461
PLM027 Pulmonary Embolism and Infarction 24 0.028
462
c MLT094 Multiple Sclerosis 3 24 0.028
463
c ADL096 Adult Hepatocellular Carcinoma 24 0.028
464
c ATR075 Atrial Fibrillation 15 24 0.028
465
CNT017 Central Nervous System Origin Vertigo 24 0.028
466
c MLT124 Multiple Sclerosis 5 23 0.028
467
HND001 Hand Dermatosis 23 0.028
468
SNG003 Single Ventricular Heart 22 0.028
469
ATM059 Autoimmune Disease 6 22 0.028
470
c CRN214 Coronary Heart Disease 5 22 0.028
471
ATR024 Atrial Fibrillation and Stroke 22 0.028
472
VRT002 Vertebral Artery Insufficiency 22 0.028
473
P CRN178 Coronary Heart Disease 6 21 0.028
474
OPP001 Opportunistic Bacterial Infectious Disease 21 0.028
475
CRB087 Cerebral Arteriosclerosis 21 0.028
476
MND006 Mondor Disease 21 0.028
477
BNR002 Bone Resorption Disease 21 0.028
478
c INF073 Inflammatory Bowel Disease 12 21 0.028
479
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.028
480
c CRN174 Coronary Heart Disease 2 20 0.028
481
c RNL016 Renal Infectious Disease 20 0.028
482
TCR004 Tacrolimus Dose Selection 20 0.028
483
c CRN177 Coronary Heart Disease 7 20 0.028
484
ACT228 Acute Radiation Syndrome 20 0.028
485
CYT018 Cytochrome P450 2d6 Variant 19 0.028
486
c CRN175 Coronary Heart Disease 4 19 0.028
487
c CRN172 Coronary Heart Disease 3 19 0.028
488
VSC009 Vascular Skin Disease 19 0.028
489
c CRN173 Coronary Heart Disease 8 18 0.028
490
CNT010 Central Nervous System Hematologic Cancer 18 0.028
491
PRM227 Primary Orthostatic Hypotension 18 0.028
492
c WVR003 Weaver Syndrome 1 18 0.028
493
c MLT093 Multiple Sclerosis 2 18 0.028
494
c CHR344 Chronic Orthostatic Intolerance 18 0.028
495
c CRN176 Coronary Heart Disease 9 18 0.028
496
PYR009 Pyridoxine Deficiency Anemia 18 0.028
497
ACT094 Acute Articular Rheumatism 17 0.028
498
c ADL079 Adult Heart Tumor 16 0.028
499
BLD072 Bleeding Disorder, East Texas Type 16 0.028
500
c DYS033 Dysautonomia Like Disorder 16 0.028
501
FMR002 Femoral Cancer 16 0.028
502
c ATR025 Atrial Fibrillation, Familial, 2 16 0.028
503
c MLT095 Multiple Sclerosis 4 16 0.028
504
ATM053 Autoimmune Disease 2 16 0.028
505
BNM008 Bone Mineral Density, Low 16 0.028
506
ATM054 Autoimmune Disease 3 15 0.028
507
ATM055 Autoimmune Disease 4 15 0.028
508
c ATR028 Atrial Fibrillation, Familial, 8 15 0.028
509
c ATR027 Atrial Fibrillation, Familial, 5 15 0.028
510
HRT029 Heart Tumor of the Child 15 0.028
511
STT044 Statin Toxicity 14 0.028
512
WSC001 Wisconsin Syndrome 14 0.028
513
NVD002 Nevada Syndrome 14 0.028
514
CGL001 Coagulation Protein Disease 14 0.028
515
NVS004 Nova Syndrome 13 0.028
516
CMP052 Complication in Hemodialysis 13 0.028
517
INB001 Inborn Amino Acid Metabolism Disorder 12 0.028
518
HRP008 Herpes Simiae 12 0.028
519
CLC050 Calciphylaxis Cutis 12 0.028
520
c BCT003 Bacterial Exanthem 11 0.028
521
TCK005 Tucker Syndrome 11 0.028
522
HRP012 Herpesvirus Simiae B Virus 10 0.028
523
PRT104 Protein S Acquired Deficiency 10 0.028
524
BNJ001 Benjamin Syndrome 9 0.028
Content
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