Search results for Peginterferon alfa-2b

577 hits were found for Peginterferon alfa-2b

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 69 0.477
2
c HPT001 Hepatitis C 68 0.435
3
c VRL010 Viral Hepatitis 60 0.395
4
c HPT003 Hepatitis a 59 0.391
5
c HPT073 Hepatitis C Virus 73 0.379
6
c HPT016 Hepatitis B 64 0.363
7
P LVR013 Liver Disease 75 0.325
8
VRL011 Viral Infectious Disease 55 0.263
9
c HPT015 Hepatitis D 52 0.201
10
HPD002 Hepadnavirus Infection 22 0.199
11
MLN008 Melanoma 62 0.180
12
c HPT007 Hepatitis E 54 0.145
13
ADM013 Adamantinoma of Long Bones 57 0.142
14
RNL101 Renal Cell Carcinoma, Papillary 63 0.129
15
P NRV006 Nervous System Cancer 60 0.129
16
P MDL005 Medulloblastoma 77 0.126
17
TST021 Testicular Germ Cell Tumor 69 0.126
18
EWN003 Ewing Sarcoma 66 0.126
19
GRM001 Germ Cell and Embryonal Cancer 36 0.126
20
P RNL014 Renal Cell Carcinoma 82 0.124
21
HRP008 Herpes Simiae 12 0.124
22
HRP012 Herpesvirus Simiae B Virus 10 0.124
23
LVR012 Liver Cirrhosis 67 0.123
24
P HPT023 Hepatocellular Carcinoma 92 0.123
25
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.120
26
CRC006 Carcinoid Syndrome 52 0.119
27
PRM097 Primary Immunodeficiency Disease 60 0.118
28
P KDN017 Kidney Cancer 65 0.118
29
NRN004 Neuroendocrine Tumor 56 0.117
30
CSY001 C Syndrome 50 0.114
31
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.112
32
CLV009 Clove Syndrome, Somatic 41 0.112
33
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.112
34
ACQ007 Acquired Immunodeficiency Syndrome 60 0.110
35
ACD009 Acid-Labile Subunit, Deficiency of 45 0.108
36
INC022 Inclusion-Cell Disease 46 0.105
37
P LKM002 Leukemia 71 0.105
38
P MLT019 Multiple Myeloma 83 0.104
39
BRN028 Brain Cancer 70 0.102
40
SKN019 Skin Melanoma 62 0.101
41
P SKN013 Skin Benign Neoplasm 43 0.101
42
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.095
43
c HMG001 Hemoglobin C Disease 47 0.092
44
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.092
45
c CLL013 Cell Type Cancer 46 0.092
46
P LYM118 Lymphoma 69 0.091
47
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.091
48
GST050 Gastrointestinal System Disease 56 0.091
49
P ESS003 Essential Thrombocythemia 70 0.089
50
HRY003 Hairy Cell Leukemia 57 0.088
51
WTH001 Withdrawal Disorder 37 0.087
52
IMM076 Immunodeficiency 24 27 0.087
53
MLG108 Malignant Melanoma, Somatic 60 0.086
54
PLS009 Plasma Cell Neoplasm 48 0.085
55
HV1006 Hiv-1 80 0.085
56
c ADL096 Adult Hepatocellular Carcinoma 24 0.084
57
c RNL016 Renal Infectious Disease 20 0.084
58
SCK003 Sickle Cell Anemia 71 0.082
59
KWS002 Kawasaki Disease 70 0.082
60
P KDN018 Kidney Disease 66 0.082
61
P HMN010 Hemangioma 59 0.082
62
IMM071 Immunodeficiency 12 26 0.082
63
OCL009 Ocular Cancer 59 0.081
64
CRY004 Cryoglobulinemia 46 0.080
65
MYC002 Mycobacterium Avium Complex Disease 52 0.079
66
SXL003 Sexual Disorder 42 0.079
67
P SPS003 Spastic Diplegia 52 0.078
68
c MCL042 Macular Degeneration, Age-Related, 1 73 0.078
69
P GST049 Gastrointestinal System Cancer 60 0.078
70
MLG088 Malignant Germ Cell Tumor 38 0.078
71
KPS004 Kaposi Sarcoma 67 0.077
72
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.077
73
DFC004 Deficiency Anemia 64 0.077
74
STM006 Stomach Disease 50 0.077
75
P INF038 Influenza 72 0.076
76
P NTR004 Neutropenia 59 0.076
77
NTR005 Nutritional Deficiency Disease 36 0.076
78
P HNT016 Huntington Disease 80 0.074
79
P MYL006 Myeloid Leukemia 66 0.074
80
SKN023 Skin Tag 44 0.074
81
HMT002 Hematologic Cancer 64 0.074
82
ALL026 Allergic Hypersensitivity Disease 52 0.073
83
c RNL034 Renal Cell Carcinoma 4 18 0.072
84
c CHR089 Chronic Kidney Failure 66 0.070
85
GRN017 Granulocytopenia 44 0.070
86
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.070
87
VSC006 Vascular Cancer 51 0.070
88
SRC014 Sarcoma 66 0.070
89
EMB004 Embryonal Carcinoma 57 0.070
90
PRP021 Peripheral Nervous System Neoplasm 46 0.070
91
ADJ001 Adjustment Disorder 38 0.069
92
MND006 Mondor Disease 21 0.069
93
BLD053 Blood Platelet Disease 46 0.069
94
IMM068 Immunodeficiency 8 30 0.069
95
LYM019 Lymphosarcoma 53 0.068
96
LYM024 Lymphatic System Disease 52 0.068
97
HRT007 Heart Cancer 46 0.068
98
c ADL001 Adult Lymphoma 39 0.068
99
P HRT017 Heart Tumor 32 0.068
100
c ADL079 Adult Heart Tumor 16 0.068
101
END030 End Stage Renal Failure 55 0.067
102
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.067
103
c NNN010 Noonan Syndrome 3 35 0.067
104
IMP003 Impaired Renal Function Disease 34 0.067
105
c TRC078 Trichohepatoenteric Syndrome 2 29 0.067
106
ACR041 Acromelic Frontonasal Dysostosis 45 0.066
107
BRT030 Birth Defects 43 0.066
108
IMM065 Immunodeficiency 10 36 0.066
109
IMM120 Immunodeficiency 40 24 0.066
110
MYC006 Mycosis Fungoides 66 0.065
111
BNC003 Bone Cancer 58 0.065
112
SZR001 Sezary's Disease 52 0.065
113
SNS023 Sensory System Cancer 43 0.065
114
NSY001 N Syndrome 36 0.065
115
c CNN010 Connective Tissue Benign Neoplasm 32 0.065
116
PRM243 Primary Bone Cancer 29 0.065
117
BNM001 Bone Marrow Cancer 51 0.065
118
P CHR562 Chronic Myelocytic Leukemia 41 0.065
119
c ALP005 Alpha Chain Disease 37 0.065
120
P CLR023 Colorectal Cancer 97 0.064
121
P ORL007 Oral Cavity Cancer 59 0.064
122
ORL011 Oral Cancer 56 0.064
123
P LYM033 Lymphoproliferative Syndrome 56 0.064
124
C3D001 C3 Deficiency 53 0.064
125
IMM136 Immune System Disease 51 0.064
126
HMN032 Human Herpesvirus 8 46 0.064
127
CTS003 Coats Disease 57 0.063
128
FDL002 Food Allergy 53 0.063
129
LKC003 Leukocyte Disease 43 0.063
130
c CHR064 Chronic Monocytic Leukemia 42 0.063
131
IMM088 Immunodeficiency 36 22 0.063
132
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.063
133
P THR014 Thrombocytopenia 64 0.063
134
IMM077 Immunodeficiency 20 27 0.063
135
P FLL037 Follicular Lymphoma 70 0.061
136
LYM020 Lymph Node Cancer 39 0.061
137
LYM023 Lymphatic System Cancer 33 0.061
138
c MLN032 Melanoma, Cutaneous Malignant, 2 31 0.061
139
P ADN016 Adenocarcinoma 69 0.061
140
PCK002 Pick Disease 68 0.061
141
P PLY018 Polycythemia 58 0.061
142
P OVR049 Ovarian Disease 56 0.061
143
FML039 Female Reproductive System Disease 48 0.061
144
ALN001 Aland Island Eye Disease 45 0.061
145
RPR002 Reproductive System Disease 41 0.061
146
BLD054 Blood Protein Disease 37 0.061
147
c THR090 Thrombocythemia 1 30 0.061
148
SQM006 Squamous Cell Carcinoma 70 0.060
149
LYM115 Lymphoma, Non-Hodgkin 63 0.060
150
c ADL017 Adult T-Cell Leukemia 60 0.060
151
P TCL004 T-Cell Leukemia 47 0.060
152
GST071 Gastrointestinal Carcinoma 42 0.060
153
MLN013 Melanoma Metastasis 40 0.060
154
c THR037 Thrombocytopenia 2 35 0.060
155
GLB003 Globe Disease 32 0.060
156
IMM074 Immunodeficiency 16 26 0.060
157
GLB001 Gilbert Syndrome 60 0.059
158
MYL031 Myeloproliferative Neoplasm 58 0.059
159
c CHR418 Chronic Leukemia 47 0.059
160
CRB002 Cerebral Primitive Neuroectodermal Tumor 41 0.059
161
MRG013 Mirage Syndrome 29 0.059
162
CLR003 Clear Cell Adenocarcinoma 56 0.057
163
c RNL003 Renal Clear Cell Carcinoma 54 0.057
164
CLR030 Clear Cell Renal Cell Carcinoma 53 0.057
165
OCL022 Ocular Melanoma 52 0.057
166
c MLN050 Melanoma, Cutaneous Malignant, 3 30 0.057
167
HRT029 Heart Tumor of the Child 15 0.057
168
P HYP086 Hypothyroidism 64 0.056
169
P HML002 Hemolytic Anemia 62 0.056
170
FCT003 Factor X Deficiency 61 0.056
171
P HYP060 Hyperinsulinism 58 0.056
172
ART002 Arts Syndrome 51 0.056
173
BCL002 B Cell Deficiency 49 0.056
174
THY030 Thyroid Gland Disease 48 0.056
175
IMM082 Immunodeficiency 18 31 0.056
176
CD4004 Cd4 Deficiency 14 0.056
177
CHR414 Chronic End-Stage Hepatitis C 12 0.056
178
P OVR042 Ovarian Cancer 76 0.055
179
c CHR090 Chronic Lymphocytic Leukemia 76 0.055
180
P HYP098 Hypereosinophilic Syndrome 63 0.055
181
PLY125 Polycythemia Vera, Somatic 63 0.055
182
P LYM026 Lymphoblastic Leukemia 62 0.055
183
FLL027 Fallopian Tube Carcinoma 60 0.055
184
FCT006 Factor V Deficiency 57 0.055
185
P SML001 Small Cell Carcinoma 56 0.055
186
SML033 Small Cell Cancer of the Lung, Somatic 54 0.055
187
FML038 Female Reproductive Organ Cancer 50 0.055
188
LYM067 Lymphoid Leukemia 44 0.055
189
P CNN004 Connective Tissue Cancer 40 0.055
190
PRT035 Peritoneum Cancer 35 0.055
191
FLL029 Fallopian Tube Disease 32 0.055
192
ILM001 Ileum Cancer 25 0.055
193
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 24 0.055
194
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.055
195
c LKM005 Leukemia, T-Cell, Chronic 20 0.055
196
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.055
197
BRC012 Brucellosis 66 0.055
198
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.055
199
P PRT013 Portal Hypertension 60 0.055
200
P HMR003 Hemorrhagic Disease 57 0.055
201
END035 Endocrine Gland Cancer 49 0.055
202
CRD118 Cardiovascular Cancer 44 0.055
203
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.055
204
P BLD051 Blood Coagulation Disease 42 0.055
205
HMT018 Hematopoietic Stem Cell Transplantation 41 0.055
206
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.055
207
VSC008 Vascular Hemostatic Disease 30 0.055
208
P BCL006 B-Cell Lymphomas 65 0.053
209
P UVL004 Uveal Melanoma 60 0.053
210
LYM116 Lymph Node Disease 47 0.053
211
FXF002 Fox-Fordyce Disease 36 0.053
212
RDT005 Radiation Induced Cancer 28 0.053
213
c MLN052 Melanoma, Cutaneous Malignant, 5 24 0.053
214
P HRT032 Heart Disease 75 0.052
215
FTT001 Fatty Liver Disease 59 0.052
216
NWC001 Newcastle Disease 54 0.052
217
NNL002 Nonalcoholic Steatohepatitis 50 0.052
218
VND001 Vein Disease 47 0.052
219
PRM025 Primary Bacterial Infectious Disease 41 0.052
220
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.052
221
IMM078 Immunodeficiency 21 35 0.052
222
IMM080 Immunodeficiency 23 27 0.052
223
GRM003 German Syndrome 22 0.052
224
IMM142 Immunodeficiency 50 20 0.052
225
P NRF002 Neurofibromatosis 71 0.050
226
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.050
227
c NRF018 Neurofibromatosis, Type 1 67 0.050
228
c NRF019 Neurofibromatosis, Type 2 62 0.050
229
CRV038 Cervical Squamous Cell Carcinoma 60 0.050
230
CRN036 Craniopharyngioma 59 0.050
231
ORL015 Oral Squamous Cell Carcinoma 57 0.050
232
NRM005 Neuromuscular Disease 56 0.050
233
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.050
234
PRP019 Peripheral Nervous System Disease 55 0.050
235
THR004 Thrombocytosis 55 0.050
236
NRF007 Neurofibroma 53 0.050
237
c PRM012 Primary Polycythemia 52 0.050
238
URN009 Urinary System Disease 50 0.050
239
P URF003 Urofacial Syndrome 1 50 0.050
240
AML029 Ameloblastoma 46 0.050
241
PLX002 Plexiform Neurofibroma 41 0.050
242
GND003 Gonadal Disease 39 0.050
243
P CNT036 Central Nervous System Germ Cell Tumor 37 0.050
244
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.050
245
MLR007 Male Reproductive System Disease 34 0.050
246
BNL002 Bone Lymphoma 32 0.050
247
GST014 Gastrointestinal Lymphoma 31 0.050
248
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.050
249
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.050
250
GRN016 Grant Syndrome 29 0.050
251
CLL006 Cellular Neurofibroma 28 0.050
252
PRM151 Primary Bone Lymphoma 26 0.050
253
YNG002 Young Syndrome 26 0.050
254
BRN049 Brain Tumor, Childhood 20 0.050
255
c CRN177 Coronary Heart Disease 7 20 0.050
256
c CRN176 Coronary Heart Disease 9 18 0.050
257
PDT020 Pediatric Germ Cell Cancer 17 0.050
258
c ADL022 Adult Central Nervous System Primitive Neuroectodermal Neoplasm 15 0.050
259
CHL055 Childhood Germ Cell Brain Tumor 15 0.050
260
PRP010 Prepuce Cancer 15 0.050
261
BNM012 Bone Ameloblastoma 11 0.050
262
HRD059 Hereditary Peripheral Nervous Disorder 11 0.050
263
SFT003 Soft Tissue Sarcoma 57 0.048
264
LYM104 Lymphoma, Malt, Somatic 54 0.048
265
P CNT005 Central Nervous System Lymphoma 53 0.048
266
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.048
267
MRG003 Marginal Zone B-Cell Lymphoma 52 0.048
268
P CTN015 Cutaneous T Cell Lymphoma 50 0.048
269
SRT004 Serotonin Syndrome 49 0.048
270
c PRM226 Primary Central Nervous System Lymphoma 49 0.048
271
SPL012 Splenic Disease 46 0.048
272
c FLL041 Follicular Lymphoma 1 45 0.048
273
SPL004 Splenic Marginal Zone Lymphoma 44 0.048
274
c HMN022 Human T-Cell Leukemia Virus Type 2 44 0.048
275
CLL014 Cll/sll 42 0.048
276
c PRM023 Pre-Malignant Neoplasm 41 0.048
277
CRC014 Carcinoid Tumors, Intestinal 40 0.048
278
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.048
279
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.048
280
P MLN043 Melanoma, Cutaneous Malignant 8 37 0.048
281
CNT018 Central Nervous System Leukemia 37 0.048
282
P GST047 Gastrointestinal Neuroendocrine Tumor 36 0.048
283
SPL011 Spleen Cancer 36 0.048
284
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.048
285
CHR079 Choroid Disease 34 0.048
286
IRS003 Iris Disease 31 0.048
287
c LKM004 Leukemia, B-Cell, Chronic 24 0.048
288
CLR122 Ciliary Body Cancer 21 0.048
289
UVL003 Uveal Diseases 18 0.048
290
c MLN041 Melanoma, Uveal 2 17 0.048
291
c HMN023 Human T-Cell Leukemia Virus Type 3 14 0.048
292
P OST012 Osteoarthritis 83 0.047
293
c LKM061 Leukemia, Acute Myeloid 73 0.047
294
MYL009 Myelodysplastic Syndrome 73 0.047
295
P LPR003 Leprosy 69 0.047
296
P GLB002 Glioblastoma 68 0.047
297
ANX002 Anxiety Disorder 67 0.047
298
P THL005 Thalassemia 64 0.047
299
GLB015 Glioblastoma Multiforme 63 0.047
300
P GLM045 Glioma 60 0.047
301
c ACT073 Acute Leukemia 60 0.047
302
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.047
303
WLL006 Wells Syndrome 59 0.047
304
P OLG002 Oligodendroglioma 56 0.047
305
P ACT135 Acute Graft Versus Host Disease 53 0.047
306
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.047
307
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.047
308
c MLG068 Malignant Glioma 51 0.047
309
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 49 0.047
310
GLM004 Gliomatosis Cerebri 49 0.047
311
QBC001 Quebec Platelet Disorder 48 0.047
312
THL018 Thalassemia Major 48 0.047
313
P TRC086 Trichohepatoenteric Syndrome 1 48 0.047
314
BRN032 Brain Glioma 48 0.047
315
GDS001 Good Syndrome 44 0.047
316
MLT001 Multiple Chemical Sensitivity 43 0.047
317
ANP009 Anaplastic Oligodendroglioma 41 0.047
318
BRN005 Brain Glioblastoma Multiforme 38 0.047
319
VSC018 Visceral Steatosis 37 0.047
320
SBS006 Sebastian Syndrome 35 0.047
321
NTR006 Neutrophil Immunodeficiency Syndrome 35 0.047
322
c ADL008 Adult Oligodendroglioma 35 0.047
323
ANG049 Angioedema Induced by Ace Inhibitors 34 0.047
324
c GLB007 Glioblastoma 3 31 0.047
325
c OST147 Osteoarthritis 1 30 0.047
326
HNS001 Hansen's Disease 30 0.047
327
ACT118 Acute Non Lymphoblastic Leukemia 30 0.047
328
P FTT008 Fatty Liver Disease, Nonalcoholic 1 30 0.047
329
IMM062 Immunodeficiency 11 26 0.047
330
BRN007 Brain Oligodendroglioma 21 0.047
331
CNT010 Central Nervous System Hematologic Cancer 18 0.047
332
c FTT007 Fatty Liver Disease, Nonalcoholic 2 16 0.047
333
c LPR016 Leprosy 4 15 0.047
334
MLG118 Malignancy Diagnosed During Pregnancy 15 0.047
335
HML018 Homologous Wasting Disease 13 0.047
336
SLT010 Solitary Necrotic Tumor of the Liver 11 0.047
337
THY021 Thyroid Malformation 11 0.047
338
P ALX003 Alexander Disease 63 0.042
339
OST085 Osteosarcoma, Somatic 63 0.042
340
P INT068 Intestinal Disease 60 0.042
341
CHL071 Child Syndrome 58 0.042
342
P LRY044 Larynx Cancer 57 0.042
343
KDS001 Kid Syndrome 53 0.042
344
P LPC002 Lip Cancer 53 0.042
345
P SML016 Small Intestine Cancer 52 0.042
346
OPT006 Optic Nerve Disease 52 0.042
347
c LRG001 Large Cell Carcinoma 51 0.042
348
UTR033 Uterine Corpus Cancer 49 0.042
349
MRS002 Marshall Syndrome 49 0.042
350
INT253 Intestinal Benign Neoplasm 47 0.042
351
ORP003 Oropharynx Cancer 45 0.042
352
MXD023 Mixed Cell Type Cancer 44 0.042
353
OVR094 Ovarian Epithelial Cancer 43 0.042
354
HYP082 Hypopharynx Cancer 43 0.042
355
SML008 Small Intestine Lymphoma 40 0.042
356
HRT010 Heart Sarcoma 37 0.042
357
OPT008 Optic Nerve Neoplasm 36 0.042
358
MLG041 Malignant Triton Tumor 36 0.042
359
LCL004 Localized Osteosarcoma 35 0.042
360
BNS001 Bone Osteosarcoma 35 0.042
361
RDN001 Reading Disorder 34 0.042
362
LRY017 Laryngeal Disease 34 0.042
363
PDT021 Pediatric Osteosarcoma 33 0.042
364
FST001 Foster-Kennedy Syndrome 31 0.042
365
SML003 Small Cell Osteogenic Sarcoma 28 0.042
366
P SML002 Small Cell Sarcoma 25 0.042
367
MLG070 Malignant Iris Melanoma 23 0.042
368
CNV007 Conventional Central Osteosarcoma 23 0.042
369
c MLN051 Melanoma, Cutaneous Malignant, 6 23 0.042
370
c CRN214 Coronary Heart Disease 5 22 0.042
371
UTR037 Uterine Corpus Sarcoma 20 0.042
372
LRY005 Laryngeal Small Cell Carcinoma 19 0.042
373
VSC009 Vascular Skin Disease 19 0.042
374
MLG061 Malignant Choroid Melanoma 19 0.042
375
MLG062 Malignant Ciliary Body Melanoma 17 0.042
376
YSY001 Yao Syndrome 17 0.042
377
c ALX006 Alexander Disease Type Ii 15 0.042
378
c ALX007 Alexander Disease Type I 15 0.042
379
LPN002 Lip and Oral Cavity Cancer 15 0.042
380
LYM126 Lymphoma Aids Related 15 0.042
381
ORP004 Oropharyngeal Cancer, Adult 12 0.042
382
P MYC007 Myocardial Infarction 79 0.042
383
GST019 Gastrointestinal Stromal Tumor 73 0.042
384
SVR004 Severe Combined Immunodeficiency 69 0.042
385
P PNM007 Pneumonia 68 0.042
386
PSY004 Psychotic Disorder 67 0.042
387
P MYL005 Myelofibrosis 67 0.042
388
c LKM062 Leukemia, Acute Lymphoblastic 64 0.042
389
P LNG064 Lung Cancer Susceptibility 3 62 0.042
390
CNN005 Connective Tissue Disease 62 0.042
391
MDD011 Mood Disorder 61 0.042
392
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.042
393
P ENC018 Encephalopathy 59 0.042
394
P GT001 Gout 58 0.042
395
P CTR002 Cataract 58 0.042
396
THR024 Thrombosis 57 0.042
397
EXF001 Exfoliation Syndrome 57 0.042
398
WST001 West Syndrome 57 0.042
399
P ACT074 Acute Lymphocytic Leukemia 56 0.042
400
HPT019 Hepatic Encephalopathy 56 0.042
401
c THR092 Thrombophilia Due to Thrombin Defect 54 0.042
402
SBS003 Substance Abuse 54 0.042
403
PLN006 Poland Syndrome 54 0.042
404
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.042
405
THL016 Thalassemias, Alpha- 53 0.042
406
OLV001 Olivopontocerebellar Atrophy 53 0.042
407
END040 Endogenous Depression 53 0.042
408
MNT002 Mental Depression 53 0.042
409
DSS008 Disease of Mental Health 52 0.042
410
HMG005 Hemoglobinopathy 52 0.042
411
PRT011 Protein C Deficiency 52 0.042
412
SCK005 Sickle Cell Disease 51 0.042
413
c LYM107 Lymphoproliferative Syndrome 2 50 0.042
414
DRG003 Drug Dependence 50 0.042
415
LRN003 Learning Disability 49 0.042
416
LPD004 Lipoid Nephrosis 48 0.042
417
MSS002 Mass Syndrome 48 0.042
418
NSD001 Nose Disease 48 0.042
419
CRN017 Coronary Thrombosis 48 0.042
420
ATN002 Autonomic Nervous System Disease 48 0.042
421
GLT021 Glutaricaciduria, Type I 46 0.042
422
P PLN008 Peeling Skin Syndrome 45 0.042
423
TCL003 T Cell Deficiency 45 0.042
424
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.042
425
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.042
426
BCK006 Back Pain 43 0.042
427
CMB003 Combined T Cell and B Cell Immunodeficiency 42 0.042
428
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.042
429
SKN022 Skin Squamous Cell Carcinoma 41 0.042
430
THL017 Thalassemia Intermedia 40 0.042
431
OPD001 Opioid Abuse 40 0.042
432
CNN002 Cannabis Abuse 40 0.042
433
GST078 Gastrointestinal Allergy 40 0.042
434
c PLN018 Peeling Skin Syndrome 2 40 0.042
435
THL010 Thalassemia Minor 39 0.042
436
SXD001 Sex Differentiation Disease 38 0.042
437
DRG001 Drug Psychosis 38 0.042
438
BNS002 Bone Structure Disease 37 0.042
439
IMM003 Immunoglobulin Alpha Deficiency 36 0.042
440
c INH004 Inherited Blood Coagulation Disease 36 0.042
441
BRN048 Brain Stem Cancer 36 0.042
442
SVR077 Severe Combined Immune Deficiency 36 0.042
443
c ACQ005 Acquired Thrombocytopenia 35 0.042
444
c PLN017 Peeling Skin Syndrome 1 34 0.042
445
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.042
446
SWL001 Swallowing Disorders 33 0.042
447
c CTR121 Cataract 25 33 0.042
448
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.042
449
P CHR084 Chromosomal Disease 32 0.042
450
c LYM106 Lymphoproliferative Syndrome 1 32 0.042
451
IMM066 Immunodeficiency 9 30 0.042
452
P SCK034 Sickle Beta Thalassemia 30 0.042
453
c PLN021 Peeling Skin Syndrome 3 29 0.042
454
PHY001 Physiological Polycythemia 28 0.042
455
RFR004 Refractory Hematologic Cancer 28 0.042
456
c HMG029 Hemoglobin Se Disease 28 0.042
457
IMM095 Immunodeficiency 35 28 0.042
458
c MYC058 Myocardial Infarction 2 28 0.042
459
IMM070 Immunodeficiency 13 27 0.042
460
FGS002 Fg Syndrome 2 26 0.042
461
c THR086 Thrombocythemia 3 25 0.042
462
IMM025 Immunoglobulin a Deficiency 2 24 0.042
463
IMM085 Immunodeficiency 25 23 0.042
464
INS009 Insulin-Resistance Type B 22 0.042
465
P CRN178 Coronary Heart Disease 6 21 0.042
466
c THR110 Thrombocytopenia 6 20 0.042
467
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.042
468
c MJR008 Major Affective Disorder 2 19 0.042
469
c CRN175 Coronary Heart Disease 4 19 0.042
470
c CTR157 Cataract 28 18 0.042
471
WHT007 White Platelet Syndrome 15 0.042
472
PRM139 Primary Melanoma of the Central Nervous System 15 0.042
473
CHR062 Chronic Erythremia 13 0.042
474
FGS003 Fg Syndrome 3 13 0.042
475
c DLT001 Delta Chain Disease 13 0.042
476
IMP007 Impairment of Oral Perception 9 0.042
477
c SCK008 Sickle Delta Beta Thalassemia 9 0.042
478
P LNG032 Lung Cancer 95 0.035
479
STR067 Stroke, Ischemic 75 0.035
480
P LFR001 Li-Fraumeni Syndrome 75 0.035
481
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.035
482
TBR010 Tuberculosis 70 0.035
483
PRP027 Peripheral Vascular Disease 68 0.035
484
DWN001 Down Syndrome 66 0.035
485
P AST007 Astrocytoma 65 0.035
486
P PLC011 Pilocytic Astrocytoma 60 0.035
487
RBR001 Roberts Syndrome 60 0.035
488
P SHR029 Short Syndrome 58 0.035
489
KND001 Kindler Syndrome 57 0.035
490
P TMT001 Timothy Syndrome 55 0.035
491
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.035
492
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.035
493
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.035
494
PST046 Post-Transplant Lymphoproliferative Disease 54 0.035
495
LYM040 Lymphoblastic Lymphoma 53 0.035
496
TLN003 Telangiectasis 52 0.035
497
IRN001 Iron Deficiency Anemia 52 0.035
498
SPN041 Spinal Cord Disease 51 0.035
499
c LKM060 Leukemia, Acute Lymphoblastic 3 50 0.035
500
OPT003 Opiate Dependence 50 0.035
501
MSC072 Muscle Cancer 49 0.035
502
NCT008 Nicotine Dependence, Protection Against 49 0.035
503
OCL006 Ocular Hypertension 48 0.035
504
SBS004 Substance Dependence 47 0.035
505
CRB085 Cerebral Hemorrhage 46 0.035
506
P CRN035 Cranial Nerve Palsy 46 0.035
507
SNS003 Sensory Peripheral Neuropathy 45 0.035
508
VSC047 Vascular Malformation 45 0.035
509
ANX004 Anoxia 43 0.035
510
c JVN009 Juvenile Pilocytic Astrocytoma 42 0.035
511
c VRL005 Viral Pneumonia 42 0.035
512
SMT002 Smooth Muscle Tumor 41 0.035
513
OPT007 Optic Nerve Glioma 41 0.035
514
DND018 Dendritic Cell Tumor 41 0.035
515
CRN031 Cranial Nerve Disease 40 0.035
516
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.035
517
SPN040 Spinal Cancer 39 0.035
518
SPN369 Spinal Disease 39 0.035
519
ORL003 Oral Tuberculosis 39 0.035
520
HYP034 Hypertensive Encephalopathy 38 0.035
521
c CHR579 Chiari Malformation Type Ii 37 0.035
522
P BRN035 Brain Stem Glioma 37 0.035
523
SPL006 Splenic Infarction 35 0.035
524
ADL053 Adult Astrocytic Tumour 35 0.035
525
PHT003 Phototoxic Dermatitis 35 0.035
526
PLM052 Pulmonary Arteriovenous Malformation 34 0.035
527
MXD032 Mixed Germ Cell Tumor 34 0.035
528
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 32 0.035
529
MXD026 Mixed Glioma 32 0.035
530
BRN036 Brain Stem Infarction 32 0.035
531
SRN001 Serine Deficiency 32 0.035
532
ORG010 Organ System Benign Neoplasm 31 0.035
533
c NRV012 Nervous System Benign Neoplasm 31 0.035
534
NRV004 Nerve Compression Syndrome 31 0.035
535
MXD025 Mixed Germ Cell Cancer 31 0.035
536
c EYL003 Eye Lymphoma 30 0.035
537
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.035
538
HRT003 Heart Lymphoma 30 0.035
539
BNM010 Bone Marrow Failure Syndrome 1 29 0.035
540
TXC008 Toxic Optic Neuropathy 29 0.035
541
DFF037 Diffuse Intrinsic Pontine Glioma 28 0.035
542
CRN033 Cranial Nerve Malignant Neoplasm 28 0.035
543
CRB031 Cerebral Arterial Disease 27 0.035
544
PLM151 Pulmonary Arteriovenous Fistulas 25 0.035
545
BNM011 Bone Marrow Failure Syndrome 2 25 0.035
546
OPT032 Optic Pathway Glioma 25 0.035
547
VSC001 Vascular Myelopathy 23 0.035
548
OPP001 Opportunistic Bacterial Infectious Disease 21 0.035
549
c JVN001 Juvenile Astrocytoma 21 0.035
550
SKL006 Skull Base Neoplasm 21 0.035
551
CMB002 Combat Disorder 21 0.035
552
CHL062 Childhood Pilocytic Astrocytoma 21 0.035
553
NLL002 Null Syndrome 20 0.035
554
SNS004 Sensory Organ Benign Neoplasm 20 0.035
555
SPC022 Specific Antibody Deficiency 18 0.035
556
STT009 Sutton Disease 2 18 0.035
557
BNM013 Bone Marrow Failure Syndrome 3 17 0.035
558
IMM141 Immunodeficiency 49 17 0.035
559
IMM118 Immunodeficiency 42 17 0.035
560
c TCL008 T-Cell Lymphoma 1a 17 0.035
561
OPT005 Optic Nerve Astrocytoma 16 0.035
562
IMM123 Immunodeficiency 39 16 0.035
563
P BNG072 Benign Peripheral Nerve Sheath Tumor 16 0.035
564
CHL024 Childhood Optic Nerve Glioma 16 0.035
565
GLC077 Glucocorticoid Therapy, Response to 16 0.035
566
c TMT004 Timothy Syndrome Type 1 16 0.035
567
ADL003 Adult Brainstem Mixed Glioma 14 0.035
568
CHL009 Childhood Cerebral Astrocytoma 14 0.035
569
c LFR004 Li-Fraumeni Syndrome 3 14 0.035
570
c ADL054 Adult Brain Stem Glioma 14 0.035
571
SPL013 Splenic Manifestation of Leukemia 14 0.035
572
LNG027 Long Bones of Lower Limb Cancer 14 0.035
573
c TMT005 Timothy Syndrome Type 2 12 0.035
574
c RNL033 Renal Carcinoma, Familial 12 0.035
575
PNS017 Pens Syndrome 12 0.035
576
PRT056 Protein R Deficiency 10 0.035
577
NRF001 Neurofibroma of Spinal Cord 9 0.035
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