Search results for "leukemia"

The MalaCard for "leukemia" has been retired.
Searching MalaCards for entries containing "leukemia"

2278 hits were found for 'leukemia'

# Family MCID Name MIFTS Score
1
P LKM002 Leukemia 77 7.421
2
c MYL006 Myeloid Leukemia 72 7.156
3
c CHR065 Chronic Myeloid Leukemia 71 5.925
4
P ACT019 Acute Myeloid Leukemia 92 5.835
5
P ACT074 Acute Lymphocytic Leukemia 75 4.897
6
c CHR090 Chronic Lymphocytic Leukemia 67 4.691
7
P ACT009 Acute Monocytic Leukemia 60 4.645
8
ACT095 Acute Biphenotypic Leukemia 56 4.644
9
ACT119 Acute Promyelocytic Leukemia 66 4.617
10
MGK001 Megakaryocytic Leukemia 56 4.370
11
P BCL009 B-Cell Chronic Lymphocytic Leukemia 66 4.242
12
P ACT020 Acute T Cell Leukemia 42 4.104
13
P JVN004 Juvenile Myelomonocytic Leukemia 69 4.093
14
c ACT073 Acute Leukemia 56 4.028
15
c ADL017 Adult T-Cell Leukemia 46 3.687
16
c LYM026 Lymphoblastic Leukemia 54 3.633
17
NTR003 Natural Killer Cell Leukemia 57 3.604
18
c ACT115 Acute Myeloid Leukemia, Adult 40 3.524
19
c TCL004 T-Cell Leukemia 50 3.508
20
HRY003 Hairy Cell Leukemia 57 3.447
21
c CHR285 Chronic Myelomonocytic Leukemia 56 3.311
22
c ACT117 Acute Myelomonocytic Leukemia 55 3.191
23
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 3.103
24
ACT098 Acute Erythroid Leukemia 38 3.046
25
c MNC007 Monocytic Leukemia 58 2.943
26
c ADL052 Adult Acute Lymphocytic Leukemia 54 2.924
27
LRG008 Large Granular Lymphocyte Leukemia 39 2.914
28
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 16 2.820
29
PRL017 Prolymphocytic Leukemia 43 2.797
30
PLS016 Plasma Cell Leukemia 49 2.796
31
c SBC004 Subacute Myeloid Leukemia 23 2.780
32
CHL061 Childhood Leukemia 38 2.724
33
P SYS004 Systemic Mastocytosis 66 2.701
34
P BCL005 B Cell Prolymphocytic Leukemia 26 2.658
35
P LKM060 Leukemia, Acute Lymphoblastic 3 44 2.606
36
CHR286 Chronic Neutrophilic Leukemia 49 2.578
37
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 9 2.545
38
NNN018 Noonan-Like Syndrome Disorder with or Without Juvenile Myelomonocytic Leukemia 20 2.535
39
CNT018 Central Nervous System Leukemia 41 2.517
40
c LKM005 Leukemia, T-Cell, Chronic 17 2.404
41
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 2.395
42
SBL003 Subleukemic Leukemia 13 2.362
43
c TCL005 T-Cell Prolymphocytic Leukemia 49 2.356
44
ACT103 Acute Lymphoblastic Leukemia, Childhood 15 2.346
45
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 14 2.341
46
LYM067 Lymphoid Leukemia 41 2.299
47
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 26 2.252
48
TST003 Testicular Leukemia 19 2.178
49
ACT113 Acute Myeloblastic Leukemia with Maturation 33 2.140
50
c CHR064 Chronic Monocytic Leukemia 23 2.129
51
ACT114 Acute Myeloblastic Leukemia Without Maturation 27 2.125
52
HCL001 Hcl-V 20 2.095
53
FML083 Familial Platelet Disorder with Associated Myeloid Malignancy 28 2.090
54
c LKM004 Leukemia, B-Cell, Chronic 16 2.090
55
NLL001 Null-Cell Leukemia 11 2.090
56
P PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 10 2.072
57
c INH015 Inherited Acute Myeloid Leukemia 18 2.065
58
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 9 2.065
59
PRG005 Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 7 2.065
60
PST004 Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 7 2.065
61
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 4 2.065
62
c HMN021 Human T-Cell Leukemia Virus Type 1 41 2.055
63
MST002 Mast-Cell Leukemia 36 1.987
64
CRB138 Core Binding Factor Acute Myeloid Leukemia 40 1.972
65
ACT177 Acute Basophilic Leukemia 38 1.945
66
ALK003 Aleukemic Leukemia Cutis 19 1.945
67
PRB001 Pre-B-Cell Acute Lymphoblastic Leukemia 40 1.937
68
P LFR001 Li-Fraumeni Syndrome 87 1.899
69
ACT097 Acute Erythroblastic Leukemia 12 1.878
70
RFR002 Refractory Hairy Cell Leukemia 14 1.868
71
NNT007 Neonatal Leukemia 23 1.864
72
c SBC006 Subacute Leukemia 12 1.841
73
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 12 1.826
74
LKM036 Leukemia, Acute Nonlymphocytic 10 1.821
75
ALK002 Aleukemic Monocytic Leukemia Cutis 9 1.821
76
c SBC015 Subacute Monocytic Leukemia 14 1.816
77
PLS003 Plasmacytic Leukemia 12 1.810
78
BLN016 Bilineal Acute Leukemia 11 1.810
79
PDT026 Pediatric T-Cell Leukemia 3 1.803
80
PRC009 Precursor T-Lymphoblastic Lymphoma/leukemia Refractory 7 1.788
81
ACT118 Acute Non Lymphoblastic Leukemia 19 1.672
82
c HMN022 Human T-Cell Leukemia Virus Type 2 39 1.623
83
c FML114 Familial Chronic Lymphocytic Leukemia 38 1.606
84
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 27 1.556
85
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 34 1.549
86
c 8P1002 8p11 Myeloproliferative Syndrome 37 1.542
87
CLL014 Cll/sll 27 1.542
88
P ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 33 1.534
89
ACT178 Acute Myeloid Leukemia with Multilineage Dysplasia 18 1.530
90
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 30 1.518
91
LKM017 Leukemia, Acute Myeloid, Reduced Survival in 24 1.518
92
c ACT197 Acute Myeloid Leukemia with T(8;16)(p11;p13) 14 1.513
93
c ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 20 1.508
94
LKM016 Leukemia, Acute Myeloid, Somatic 19 1.508
95
ALK014 Aleukemic Mast Cell Leukemia 12 1.508
96
LKM058 Leukemia, Acute Lymphoblastic, Somatic 14 1.503
97
c FML095 Familial Acute Lymphocytic Leukemia 10 1.503
98
c ACT106 Acute Myeloblastic Leukemia Type 1 6 1.503
99
c ACT107 Acute Myeloblastic Leukemia Type 2 6 1.503
100
P ACT108 Acute Myeloblastic Leukemia Type 3 6 1.503
101
c ACT110 Acute Myeloblastic Leukemia Type 5 6 1.503
102
c ACT111 Acute Myeloblastic Leukemia Type 6 6 1.503
103
c ACT112 Acute Myeloblastic Leukemia Type 7 6 1.503
104
MYL050 Myeloid Leukemia, Acute, M4/m4eo Subtype, Somatic 15 1.497
105
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 13 1.497
106
c ACT109 Acute Myeloblastic Leukemia Type 4 5 1.497
107
TCL015 T-Cell Acute Lymphoblastic Leukemia, Somatic 16 1.491
108
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 12 1.491
109
c ACT198 Acute Myeloid Leukemia with T(6;9)(p23;q34) 11 1.491
110
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 8 1.485
111
c HMN023 Human T-Cell Leukemia Virus Type 3 7 1.485
112
ACT116 Acute Myeloid Leukemia, Childhood 4 1.485
113
P LKM024 Leukemia/lymphoma, T-Cell 10 1.478
114
SPL013 Splenic Manifestation of Leukemia 7 1.478
115
c MYL018 Myelocytic Leukemia-Like Syndrome, Familial, Chronic 4 1.478
116
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 8 1.470
117
P FML115 Familial Chronic Myelocytic Leukemia 5 1.470
118
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 2 1.470
119
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 12 1.460
120
c NPM001 Npm1-Related Acute Myeloid Leukemia 10 1.460
121
HRY001 Hairy Cell Leukemia of Spleen 9 1.460
122
c LYM061 Lymphocytic Leukemia, Acute T-Cell 9 1.460
123
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 8 1.460
124
LKM026 Leukemia, Acute Myeloid, Therapy-Related 8 1.460
125
c LKM050 Leukemia, Chronic Lymphocytic 1 8 1.460
126
c LKM051 Leukemia, Chronic Lymphocytic 3 8 1.460
127
c LKM052 Leukemia, Chronic Lymphocytic 5 8 1.460
128
c LKM053 Leukemia, Chronic Lymphocytic 4 8 1.460
129
c LKM054 Leukemia, Acute Lymphocytic 1 8 1.460
130
c LKM056 Leukemia, Chronic Lymphocytic 2 8 1.460
131
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 8 1.460
132
c LKM055 Leukemia, Acute Lymphoblastic 2 6 1.460
133
c LKM009 Leukemia/lymphoma, B-Cell, 2 6 1.460
134
c LKM010 Leukemia/lymphoma, B-Cell, 3 6 1.460
135
LKM018 Leukemia, T-Cell Acute Lymphoblastoid 6 1.460
136
LKM023 Leukemia, Myeloid/lymphoid or Mixed-Lineage 6 1.460
137
BND002 B- and T-Cell Mixed Leukemia 6 1.460
138
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 5 1.460
139
LKM008 Leukemia, Acute Pre-B-Cell 5 1.460
140
LKM020 Leukemia, Acute Myeloid, with Eosinophilia 5 1.460
141
TCL013 T-Cell Prolymphocytic Leukemia, Somatic 5 1.460
142
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 5 1.460
143
CHL029 Childhood Precursor T-Lymphoblastic Lymphoma/leukemia 5 1.460
144
CLS019 Classic Mast Cell Leukemia 5 1.460
145
c PRC017 Precursor Lymphoblastic Lymphoma/leukemia 5 1.460
146
LKM019 Leukemia, Philadelphia Chromosome-Positive, Resistant to Imatinib 4 1.460
147
LKM022 Leukemia, Acute Promyelocytic, Pml/rara Type 4 1.460
148
LKM035 Leukemia, Acute Promyelocytic, Stat5b/rara Type 4 1.460
149
LKM037 Leukemia, Acute Promyelocytic, Numa/rara Type 4 1.460
150
LKM038 Leukemia, Acute Promyelocytic, Npm/rara Type 4 1.460
151
LKM039 Leukemia, Acute Promyelocytic, Pl2f/rara Type 4 1.460
152
LKM057 Leukemia, Post-Chemotherapy 4 1.460
153
c LYM062 Lymphoma/leukemia, B-Cell, Variant 4 1.460
154
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 4 1.460
155
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 4 1.460
156
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 4 1.460
157
c FML096 Familial Acute Myelocytic Leukemia 4 1.460
158
SPL002 Splenic Manifestation of Prolymphocytic Leukemia 4 1.460
159
SPL010 Splenic Manifestation of Hairy Cell Leukemia 4 1.460
160
LKM034 Leukemia, Transient, of Down Syndrome 3 1.460
161
ACT196 Acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2) 2 1.460
162
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 2 1.460
163
LYM040 Lymphoblastic Lymphoma 54 1.320
164
P HYP098 Hypereosinophilic Syndrome 61 1.194
165
P FML045 Familial Mosaic Monosomy 7 Syndrome 17 1.103
166
EMB016 Emberger Syndrome 25 1.082
167
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 20 1.082
168
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 17 1.070
169
NSY001 N Syndrome 33 1.045
170
CRB137 Cerebral Creatine Deficiency Syndrome 27 1.032
171
WTL001 Wt Limb Blood Syndrome 23 1.032
172
MYL040 Myelodysplastic Syndromes 79 0.304
173
HMT018 Hematopoietic Stem Cell Transplantation 40 0.215
174
c MYL007 Myeloma 61 0.191
175
SRC014 Sarcoma 69 0.179
176
END072 Endotheliitis 50 0.169
177
P MLT019 Multiple Myeloma 82 0.161
178
DWN001 Down Syndrome 61 0.151
179
P GRF002 Graft Versus Host Disease 60 0.148
180
P MYL005 Myelofibrosis 72 0.144
181
c WLM002 Wilms Tumor 51 0.141
182
HDG007 Hodgkin's Lymphoma 92 0.139
183
c NTR004 Neutropenia 64 0.138
184
THR013 Thoracic Outlet Syndrome 52 0.136
185
c HPT021 Hepatitis 64 0.133
186
P BCL006 B-Cell Lymphomas 49 0.133
187
LYM019 Lymphosarcoma 54 0.129
188
P BRS047 Breast Cancer 100 0.128
189
c MST009 Mastocytosis 71 0.128
190
c MYL014 Myeloproliferative Disorder 52 0.127
191
SYN053 Syndromic Diarrhea 32 0.127
192
P ESN007 Eosinophilia 61 0.123
193
MYL003 Myeloid Sarcoma 56 0.122
194
P HML002 Hemolytic Anemia 66 0.121
195
HYP004 Hypercalcemia 65 0.121
196
RFR010 Refractory Anemia 48 0.121
197
BRK003 Burkitt's Lymphoma 77 0.117
198
NNH001 Non-Hodgkin Lymphoma 66 0.117
199
P HST010 Histiocytosis 62 0.115
200
c ATM010 Autoimmune Hemolytic Anemia 60 0.113
201
P ATX002 Ataxia Telangiectasia 86 0.112
202
c BNG076 Benign Exophthalmos Syndrome 22 0.111
203
P RHM011 Rheumatoid Arthritis 93 0.109
204
ANK002 Ankylosing Spondylitis 74 0.109
205
P ART022 Arthritis 75 0.108
206
P ANG001 Angelman Syndrome 70 0.108
207
ART019 Aortic Valve Stenosis 64 0.108
208
ACN002 Acanthosis Nigricans 69 0.106
209
P APL001 Aplastic Anemia 82 0.105
210
P ATX010 Ataxia Neuropathy Spectrum 41 0.105
211
SVR004 Severe Combined Immunodeficiency 80 0.104
212
c THR014 Thrombocytopenia 70 0.104
213
c MNN013 Meningitis 68 0.103
214
PRS047 Prostatitis 60 0.103
215
c ESS003 Essential Thrombocythemia 59 0.103
216
P PNM007 Pneumonia 76 0.102
217
PRR002 Pure Red-Cell Aplasia 54 0.102
218
BNM005 Bone Marrow Necrosis 39 0.102
219
RCH001 Richter's Syndrome 35 0.102
220
ASP006 Aspergillosis 72 0.100
221
c PLY018 Polycythemia 61 0.100
222
LKS001 Leukostasis 49 0.100
223
PLY001 Polycythemia Vera 82 0.099
224
VSC011 Vasculitis 66 0.099
225
P NRF002 Neurofibromatosis 93 0.097
226
DSS009 Disseminated Intravascular Coagulation 62 0.097
227
SPS019 Spastic Paraparesis 41 0.096
228
SPS057 Spasticity 37 0.096
229
MNT001 Mantle Cell Lymphoma 64 0.095
230
MCR004 Macroglobulinemia 54 0.093
231
HPT023 Hepatocellular Carcinoma 79 0.092
232
P HMP002 Hemophagocytic Lymphohistiocytosis 63 0.092
233
TTR011 Tetraploidy 61 0.092
234
c THY032 Thyroiditis 66 0.091
235
THR004 Thrombocytosis 59 0.091
236
TRP002 Tropical Spastic Paraparesis 55 0.091
237
CRB009 Cerebritis 39 0.091
238
AND002 Androgen Insensitivity Syndrome 80 0.090
239
c AXN002 Axenfeld-Rieger Syndrome 66 0.090
240
P FNC001 Fanconi's Anemia 65 0.088
241
GLC037 Glucocorticoid Resistance 46 0.088
242
P RTN024 Retinoblastoma 81 0.087
243
P MLN008 Melanoma 63 0.087
244
NRP001 Neuropathy 61 0.087
245
P SVR003 Severe Congenital Neutropenia 50 0.087
246
LKM001 Leukemoid Reaction 49 0.087
247
c NNN003 Noonan Syndrome 73 0.086
248
ART001 Arterial Tortuosity Syndrome 54 0.086
249
RTN023 Retinitis 53 0.086
250
AND003 Andersen-Tawil Syndrome 53 0.086
251
MDS022 Mediastinitis 46 0.086
252
c MLG054 Malignant Histiocytosis 63 0.084
253
DPH001 Diphtheria 58 0.084
254
BCT015 Bacteremia 48 0.084
255
TFT003 Tufting Enteropathy 28 0.084
256
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.084
257
P DBT005 Diabetes Insipidus 57 0.083
258
P PNC001 Pancytopenia 48 0.082
259
P PRS040 Prostate Cancer 87 0.080
260
c ATX004 Ataxia 58 0.080
261
P GLM007 Glomerulonephritis 68 0.079
262
GNG013 Gingivitis 62 0.079
263
P ADN016 Adenocarcinoma 58 0.079
264
c ACR001 Aicardi-Goutieres Syndrome 53 0.079
265
c ACT135 Acute Graft Versus Host Disease 50 0.079
266
MYL046 Myelodysplastic Syndrome, Somatic 36 0.079
267
PRP030 Purpura 64 0.077
268
HMT002 Hematologic Cancer 61 0.077
269
P DFF005 Diffuse Large B-Cell Lymphoma 60 0.077
270
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 56 0.077
271
GRN017 Granulocytopenia 47 0.077
272
P NRB001 Neuroblastoma 70 0.076
273
SMT015 Smith Magenis Syndrome 56 0.076
274
LNG024 Langerhans-Cell Histiocytosis 56 0.076
275
BLS007 Blastic Plasmacytoid Dendritic Cell 44 0.076
276
P LNG032 Lung Cancer 72 0.074
277
P INF038 Influenza 68 0.074
278
CHR066 Chronic Fatigue Syndrome 64 0.074
279
HMG002 Hemoglobinuria 52 0.074
280
ADS002 Adie Syndrome 35 0.074
281
HNM002 Hinman Syndrome 27 0.074
282
P MLT020 Multiple Sclerosis 69 0.073
283
MYC006 Mycosis Fungoides 66 0.073
284
HV1006 Hiv-1 61 0.073
285
MYC002 Mycobacterium Avium Complex Disease 58 0.073
286
HYP266 Hypoxia 57 0.073
287
P PLM006 Pulmonary Alveolar Proteinosis 53 0.073
288
SPL018 Splenomegaly 46 0.073
289
c CHR417 Chronic Graft Versus Host Disease 43 0.073
290
P HRP006 Herpes Simplex 66 0.071
291
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.071
292
ZYG002 Zygomycosis 44 0.071
293
EMN001 Emanuel Syndrome 36 0.071
294
AND005 Androgen Insensitivity Syndrome, Mild 21 0.071
295
P OBS005 Obesity 89 0.069
296
c PNC044 Pancreatitis 69 0.069
297
c SRC013 Sarcoidosis 68 0.069
298
P HPT001 Hepatitis C 66 0.069
299
INV001 Invasive Aspergillosis 52 0.069
300
NRN002 Neuronitis 43 0.069
301
IPX001 Ipex Syndrome 37 0.069
302
HYP084 Hypopyon 26 0.069
303
SPS077 Sepsis 70 0.068
304
DRM006 Dermatitis 69 0.068
305
ABT001 Abetalipoproteinemia 64 0.068
306
P PLY019 Polyneuropathy 60 0.068
307
BLN003 Blindness 52 0.068
308
HST016 Histiocytic Sarcoma 52 0.068
309
c CNT035 Central Nervous System Disease 49 0.068
310
TBR010 Tuberculosis 83 0.066
311
c HPT016 Hepatitis B 68 0.066
312
c UVT001 Uveitis 65 0.066
313
DFC004 Deficiency Anemia 62 0.066
314
P ANP001 Anaplastic Large Cell Lymphoma 62 0.066
315
c PRP029 Porphyria 61 0.066
316
URT039 Urticaria 61 0.066
317
P CND004 Candidiasis 61 0.066
318
OST003 Osteonecrosis 58 0.066
319
P CRV039 Cervicitis 57 0.066
320
P RFR008 Refractory Anemia with Excess Blasts 34 0.066
321
P SYS001 Systemic Lupus Erythematosus 85 0.064
322
P GST019 Gastrointestinal Stromal Tumor 82 0.064
323
P MNN012 Meningioma 78 0.064
324
c LPS004 Lupus Erythematosus 72 0.064
325
P FRD001 Friedreich Ataxia 66 0.064
326
P FTL006 Fetal Alcohol Spectrum Disorder 64 0.064
327
P RNL014 Renal Cell Carcinoma 62 0.064
328
CTN014 Cutaneous Mastocytosis 61 0.064
329
PLS025 Plasmablastic Lymphoma 53 0.064
330
P THR090 Thrombocythemia 1 52 0.064
331
P SDR003 Sideroblastic Anemia 44 0.064
332
MN1001 Mn1 21 0.064
333
P HYP075 Hypertension 85 0.062
334
P PRP003 Porphyria Cutanea Tarda 75 0.062
335
P RBN001 Rubinstein-Taybi Syndrome 75 0.062
336
P NJM001 Nijmegen Breakage Syndrome 69 0.062
337
PMP001 Pemphigus 60 0.062
338
IDP064 Idiopathic Neutropenia 60 0.062
339
HYP063 Hypersplenism 58 0.062
340
HRP004 Herpes Zoster 57 0.062
341
P CTN015 Cutaneous T Cell Lymphoma 51 0.062
342
P CHR092 Chronic Myeloproliferative Disease 50 0.062
343
P FLL037 Follicular Lymphoma 46 0.062
344
LKP004 Leukopenia 44 0.062
345
RTC005 Reticulosarcoma 43 0.062
346
FLL019 Follicular Mucinosis 39 0.062
347
GRF001 Graft-Versus-Host Disease, Protection Against 31 0.062
348
c TTR021 Tetrasomy 21 29 0.062
349
FSR001 Fusariosis 28 0.062
350
c PRM041 Primary Cortisol Resistance 21 0.062
351
P AMY001 Amyotrophic Lateral Sclerosis 98 0.061
352
INF030 Infectious Mononucleosis 84 0.061
353
c DBT009 Diabetes Mellitus 78 0.061
354
GLN003 Glanzmann's Thrombasthenia 73 0.061
355
P RSP003 Respiratory Failure 68 0.061
356
RHB003 Rhabdomyosarcoma 57 0.061
357
PLS011 Plasmacytoma 57 0.061
358
c KBK001 Kabuki Syndrome 55 0.061
359
P JVN003 Juvenile Xanthogranuloma 53 0.061
360
P PRP023 Peripheral Neuropathy 52 0.061
361
OST019 Osteosclerosis 51 0.061
362
P PND001 Pain Disorder 48 0.061
363
c HPT073 Hepatitis C Virus 45 0.061
364
HYP025 Hyperphosphatemia 42 0.061
365
c PRM002 Primary Hyperoxaluria 72 0.059
366
P AST007 Astrocytoma 71 0.059
367
HYP066 Hyperglycemia 62 0.059
368
SCB001 Scabies 59 0.059
369
PRC012 Pericardial Effusion 58 0.059
370
INT221 Intravascular Large B-Cell Lymphoma 53 0.059
371
P EWN002 Ewing's Family of Tumors 48 0.059
372
URT008 Urticaria Pigmentosa 47 0.059
373
SFT003 Soft Tissue Sarcoma 45 0.059
374
CYT008 Cytomegalovirus Infection 43 0.059
375
P CLN016 Colon Cancer 78 0.057
376
P FML018 Familial Mediterranean Fever 74 0.057
377
GLL008 Gilles De La Tourette Syndrome 70 0.057
378
ATM004 Autoimmune Thrombocytopenic Purpura 68 0.057
379
PRT039 Proteinuria 57 0.057
380
PRT011 Protein C Deficiency 55 0.057
381
THY009 Thyroid Lymphoma 54 0.057
382
KLN001 Klinefelter's Syndrome 52 0.057
383
CLN015 Colon Adenocarcinoma 51 0.057
384
P GRM009 Germ Cell Tumors 49 0.057
385
PYM001 Pyomyositis 47 0.057
386
LCT001 Lactic Acidosis 46 0.057
387
BCK006 Back Pain 38 0.057
388
VRL011 Viral Infectious Disease 36 0.057
389
3Q2002 3q21q26 Syndrome 28 0.057
390
P RTT002 Rett Syndrome 82 0.055
391
ADN001 Adenosine Deaminase Deficiency 69 0.055
392
P RTH001 Rothmund-Thomson Syndrome 68 0.055
393
c ENC004 Encephalitis 65 0.055
394
FLT001 Felty's Syndrome 63 0.055
395
PRP007 Priapism 60 0.055
396
P PTT014 Pitt-Hopkins Syndrome 59 0.055
397
CLL003 Cellulitis 58 0.055
398
PRM163 Primary Mediastinal Large B-Cell Lymphoma 53 0.055
399
AGG002 Aggressive Systemic Mastocytosis 52 0.055
400
GRN007 Granuloma Annulare 52 0.055
401
LYM051 Lymphomatoid Granulomatosis 49 0.055
402
PRP036 Peripheral T-Cell Lymphoma 48 0.055
403
P MLG081 Malignant Teratoma 46 0.055
404
5QS001 5q- Syndrome 45 0.055
405
FLL036 Follicular Dendritic Cell Tumor 42 0.055
406
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.055
407
ECT004 Ecthyma 27 0.055
408
CRH001 Crohn's Disease 74 0.052
409
P AMY004 Amyloidosis 67 0.052
410
P THY023 Thymoma 66 0.052
411
P OLG002 Oligodendroglioma 64 0.052
412
BRN028 Brain Cancer 62 0.052
413
HPT022 Hepatoblastoma 62 0.052
414
ACQ007 Acquired Immunodeficiency Syndrome 61 0.052
415
PLY041 Polymyositis 58 0.052
416
CRY004 Cryoglobulinemia 57 0.052
417
P SNS014 Sinusitis 57 0.052
418
TNS005 Tonsillitis 57 0.052
419
CYT005 Cytomegalovirus Retinitis 56 0.052
420
P END033 Endocarditis 56 0.052
421
PSD002 Pseudotumor Cerebri 55 0.052
422
P INF032 Infertility 55 0.052
423
PRN049 Paraneoplastic Pemphigus 49 0.052
424
HYP017 Hypophosphatemia 48 0.052
425
MMB001 Membranoproliferative Glomerulonephritis 47 0.052
426
HYP005 Hypokalemia 47 0.052
427
EVN001 Evans' Syndrome 46 0.052
428
DNR001 Duane Retraction Syndrome 45 0.052
429
ANP009 Anaplastic Oligodendroglioma 43 0.052
430
P DNS004 Duane Syndrome Type 2 39 0.052
431
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 32 0.052
432
OTP003 Oto-Palatal-Digital Syndrome 16 0.052
433
P MYC007 Myocardial Infarction 92 0.050
434
P CLR023 Colorectal Cancer 73 0.050
435
c CWD001 Cowden Disease 71 0.050
436
P PLL001 Pallister-Hall Syndrome 70 0.050
437
PYR013 Pyruvate Kinase Deficiency 65 0.050
438
P HYP117 Hypertriglyceridemia 65 0.050
439
P LPS002 Liposarcoma 61 0.050
440
BRN002 Bronchiolitis 60 0.050
441
BRN012 Bronchiolitis Obliterans 59 0.050
442
MLL005 Miller-Dieker Syndrome 59 0.050
443
MLT022 Malt Lymphoma 58 0.050
444
EXT010 Extramedullary Plasmacytoma 58 0.050
445
MGL001 Megaloblastic Anemia 57 0.050
446
ACT100 Acute Febrile Neutrophilic Dermatosis 56 0.050
447
DND002 Dendritic Cell Sarcoma 56 0.050
448
P EXN002 Exanthem 55 0.050
449
CRD001 Cardiac Tamponade 55 0.050
450
PLY020 Polyradiculoneuropathy 55 0.050
451
c TRT010 Teratoma 55 0.050
452
PST062 Pustulosis Palmaris Et Plantaris 54 0.050
453
PRN011 Pernicious Anemia 53 0.050
454
MNN014 Mononeuritis 51 0.050
455
P NRV007 Nervous System Disease 50 0.050
456
TLN003 Telangiectasis 49 0.050
457
P HML001 Hemolytic-Uremic Syndrome 48 0.050
458
PNN001 Panniculitis 46 0.050
459
GLM011 Glomerulosclerosis 46 0.050
460
LYM045 Lymphocytic Vasculitis 44 0.050
461
PLY100 Polyploidy 43 0.050
462
IMR001 Imerslund-Grasbeck Syndrome 37 0.050
463
BNM001 Bone Marrow Cancer 34 0.050
464
FCT013 Factor V Leiden Thrombophilia 33 0.050
465
TRS012 Trisomy 22 29 0.050
466
c LYM034 Lymphoproliferative Disease, X-Linked 29 0.050
467
c HRD009 Hereditary Wilms' Tumor 22 0.050
468
ACT176 Acute Panmyelosis with Myelofibrosis 22 0.050
469
c TCL008 T-Cell Lymphoma 1a 12 0.050
470
P ALZ001 Alzheimer's Disease 97 0.048
471
KPS001 Kaposi's Sarcoma 85 0.048
472
P OST018 Osteosarcoma 79 0.048
473
P LPR002 Leopard Syndrome 73 0.048
474
c THL005 Thalassemia 72 0.048
475
P KDN017 Kidney Cancer 68 0.048
476
c NPH012 Nephrotic Syndrome 66 0.048
477
P NNN008 Noonan Syndrome 1 66 0.048
478
MYS005 Myositis 66 0.048
479
CLD007 Cold Agglutinin Disease 60 0.048
480
c AGM001 Agammaglobulinemia 60 0.048
481
P AVS004 Avascular Necrosis of the Femoral Head 59 0.048
482
NTR001 Neutral Lipid Storage Disease 59 0.048
483
DNG003 Dengue Disease 59 0.048
484
GLB015 Glioblastoma Multiforme 59 0.048
485
NRH001 Neurohypophyseal Diabetes Insipidus 56 0.048
486
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 55 0.048
487
PYD001 Pyoderma Gangrenosum 55 0.048
488
VNS009 Venous Thrombosis 55 0.048
489
P THR012 Thoracic Cancer 55 0.048
490
MRK001 Merkel Cell Carcinoma 53 0.048
491
c ACT134 Acute Liver Failure 53 0.048
492
c CPL003 Capillary Leak Syndrome 52 0.048
493
PYD002 Pyoderma 51 0.048
494
LYM027 Lymphopenia 51 0.048
495
c MSB002 Mesoblastic Nephroma 50 0.048
496
c CNG029 Congenital Mesoblastic Nephroma 48 0.048
497
P SPR035 Superior Vena Cava Syndrome 42 0.048
498
ANG046 Angioimmunoblastic T-Cell Lymphoma 40 0.048
499
NRG004 Neurogenic Diabetes Insipidus 39 0.048
500
CMP001 Composite Lymphoma 39 0.048
501
SPL006 Splenic Infarction 39 0.048
502
ANG037 Angiomatosis 38 0.048
503
P SRC025 Sarcoidosis 1 36 0.048
504
ACQ031 Acquired Idiopathic Sideroblastic Anemia 29 0.048
505
CYT004 Cytomegalic Inclusion Disease 26 0.048
506
CD4007 Cd4+/cd56+ Hematodermic Neoplasm 24 0.048
507
P HMC003 Hemochromatosis 78 0.045
508
P MDL005 Medulloblastoma 77 0.045
509
P FCL005 Focal Segmental Glomerulosclerosis 72 0.045
510
P ATM006 Autoimmune Lymphoproliferative Syndrome 66 0.045
511
ANT006 Antiphospholipid Syndrome 65 0.045
512
THR079 Thromboembolism 64 0.045
513
STR008 Strongyloidiasis 64 0.045
514
c ACT027 Acute Pancreatitis 63 0.045
515
PST046 Post-Transplant Lymphoproliferative Disease 60 0.045
516
PRM027 Primitive Neuroectodermal Tumor 60 0.045
517
MYX005 Myxoid Liposarcoma 58 0.045
518
OST017 Osteomyelitis 58 0.045
519
MRG003 Marginal Zone B-Cell Lymphoma 57 0.045
520
c PST005 Posterior Uveitis 56 0.045
521
LRY018 Laryngeal Squamous Cell Carcinoma 56 0.045
522
APP008 Appendicitis 55 0.045
523
PRC013 Pericarditis 53 0.045
524
RTN001 Retinal Vasculitis 50 0.045
525
P ALV004 Alveolar Rhabdomyosarcoma 49 0.045
526
LYM021 Lymphadenitis 47 0.045
527
PRN039 Paraneoplastic Syndromes 46 0.045
528
GYN001 Gynecomastia 46 0.045
529
ANR040 Aneurysm 44 0.045
530
MLG083 Male Germ Cell Tumor 44 0.045
531
SPN060 Spondylocarpotarsal Synostosis Syndrome 42 0.045
532
P WLM008 Wilms Tumor, Type 1 38 0.045
533
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 37 0.045
534
BLT011 Bilateral Perisylvian Polymicrogyria 34 0.045
535
MTR008 Mature B-Cell Neoplasm 31 0.045
536
NRW001 Norwegian Scabies 31 0.045
537
GLM037 Glioma Somatic 30 0.045
538
HPT070 Hepatosplenic T-Cell Lymphoma 26 0.045
539
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 26 0.045
540
IRN002 Iron Metabolism Disease 26 0.045
541
c RNG017 Ring Chromosome 21 24 0.045
542
RFR007 Refractory Anemia with Excess Blasts in Transformation 21 0.045
543
SKN016 Skin Disease 75 0.043
544
THY028 Thyroid Cancer 73 0.043
545
P TMP003 Temporal Arteritis 71 0.043
546
SHW002 Shwachman-Diamond Syndrome 68 0.043
547
P MLG075 Malignant Mesothelioma 67 0.043
548
P BCK002 Beckwith-Wiedemann Syndrome 67 0.043
549
c JVN010 Juvenile Rheumatoid Arthritis 65 0.043
550
P LMY004 Leiomyosarcoma 64 0.043
551
ULC004 Ulcerative Colitis 63 0.043
552
ACT049 Acute Disseminated Encephalomyelitis 63 0.043
553
HYP056 Hypoglycemia 63 0.043
554
P FBR017 Fibrosarcoma 63 0.043
555
c MYP004 Myopathy 62 0.043
556
SRS001 Serous Cystadenocarcinoma 60 0.043
557
SPT013 Septic Shock 60 0.043
558
P END047 Endophthalmitis 59 0.043
559
c ACT075 Acute Myocardial Infarction 59 0.043
560
ADN011 Adenoid Cystic Carcinoma 57 0.043
561
c JBR001 Joubert Syndrome 57 0.043
562
PLM020 Pleomorphic Xanthoastrocytoma 57 0.043
563
P FNC044 Fanconi Anemia, Complementation Group C 57 0.043
564
P RPD001 Rapidly Progressive Glomerulonephritis 57 0.043
565
ORL005 Oral Candidiasis 56 0.043
566
c CNT016 Central Retinal Vein Occlusion 55 0.043
567
P JBR004 Joubert Syndrome 2 55 0.043
568
TLP001 Talipes Equinovarus 55 0.043
569
RDC002 Radiculopathy 55 0.043
570
CRD005 Cardia Cancer 54 0.043
571
GST050 Gastrointestinal System Disease 54 0.043
572
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 53 0.043
573
ENC006 Encephalomyelitis 52 0.043
574
NRF008 Neurofibromatosis-Noonan Syndrome 52 0.043
575
GRW007 Growth Hormone Deficiency 52 0.043
576
RSC001 Rosacea 50 0.043
577
OBS001 Obstructive Jaundice 50 0.043
578
PRT026 Parotitis 50 0.043
579
P WLD002 Waldenstrom Macroglobulinemia 49 0.043
580
c PRM046 Primary Malignant Lymphoma 48 0.043
581
THY022 Thymic Carcinoma 48 0.043
582
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.043
583
PRM097 Primary Immunodeficiency Disease 46 0.043
584
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 46 0.043
585
LKP003 Leukoplakia 46 0.043
586
THR035 Thrombasthenia 45 0.043
587
LYM012 Lymphoplasmacytic Lymphoma 44 0.043
588
TCL003 T Cell Deficiency 44 0.043
589
SPR033 Superficial Spreading Melanoma 43 0.043
590
EPG003 Epiglottitis 41 0.043
591
P LSS005 Lissencephaly 1 39 0.043
592
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 34 0.043
593
CLC008 Colchicine Resistance 31 0.043
594
SPL007 Splenic Abscess 30 0.043
595
PNM003 Pneumatosis Cystoides Intestinalis 26 0.043
596
EXF003 Exfoliative Dermatitis 25 0.043
597
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 22 0.043
598
GLC006 Galactosemia 81 0.040
599
ESP021 Esophageal Cancer 80 0.040
600
P MYS003 Myasthenia Gravis 78 0.040
601
c BTT002 Beta Thalassemia 77 0.040
602
P GCH001 Gaucher's Disease 77 0.040
603
BLM001 Bloom Syndrome 74 0.040
604
HST011 Histoplasmosis 73 0.040
605
P CRD013 Cardiofaciocutaneous Syndrome 72 0.040
606
P CHR071 Charcot-Marie-Tooth Disease 70 0.040
607
LKC001 Leukocyte Adhesion Deficiency 68 0.040
608
MSL001 Measles 67 0.040
609
c HMP007 Hemophilia 67 0.040
610
HPT002 Hepatic Vein Thrombosis 66 0.040
611
P INS005 Insulin Resistance 66 0.040
612
ADN018 Adenoma 64 0.040
613
P CNJ013 Conjunctivitis 63 0.040
614
P ADL010 Adult Respiratory Distress Syndrome 63 0.040
615
P ART023 Arthropathy 63 0.040
616
P ESP024 Esophagitis 63 0.040
617
CMP002 Campylobacteriosis 63 0.040
618
P STM004 Stomach Cancer 63 0.040
619
CMM004 Common Variable Immunodeficiency 63 0.040
620
PSR002 Psoriasis 63 0.040
621
c HYP076 Hyperthyroidism 62 0.040
622
c HRD010 Hereditary Spastic Paraplegia 61 0.040
623
ANT009 Antithrombin Iii Deficiency 60 0.040
624
CHL067 Cholecystitis 60 0.040
625
CHC001 Chickenpox 60 0.040
626
c ALM001 Al Amyloidosis 59 0.040
627
MLR002 Miliary Tuberculosis 59 0.040
628
SCK005 Sickle Cell Disease 58 0.040
629
INT054 Intraocular Lymphoma 58 0.040
630
END030 End Stage Renal Failure 58 0.040
631
PRN001 Purine Nucleoside Phosphorylase Deficiency 57 0.040
632
P MYC008 Myocarditis 57 0.040
633
GLL022 Guillain-Barre Syndrome 57 0.040
634
P RTN022 Retinal Vein Occlusion 56 0.040
635
c PRM011 Primary Ciliary Dyskinesia 56 0.040
636
EPD001 Epidermodysplasia Verruciformis 56 0.040
637
NCR004 Nocardiosis 56 0.040
638
CHR008 Choroiditis 55 0.040
639
NPH051 Nephritis 54 0.040
640
ORL011 Oral Cancer 53 0.040
641
SPT004 Septic Arthritis 53 0.040
642
LMB024 Limbic Encephalitis 53 0.040
643
STN007 Stenotrophomonas Maltophilia 52 0.040
644
HYP037 Hyperhomocysteinemia 51 0.040
645
HPT032 Hepatocellular Carcinoma, Somatic 51 0.040
646
GST027 Gastric Lymphoma 50 0.040
647
MCR020 Microsporidiosis 49 0.040
648
GNG002 Ganglioneuroma 49 0.040
649
PRN029 Parainfluenza Virus Type 3 48 0.040
650
SPL004 Splenic Marginal Zone Lymphoma 47 0.040
651
OVR012 Ovarian Serous Cystadenocarcinoma 46 0.040
652
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 46 0.040
653
UTR043 Uterine Sarcoma 45 0.040
654
OLG015 Oligoarticular Juvenile Arthritis 43 0.040
655
HDR003 Hidradenitis 43 0.040
656
CDQ001 Cauda Equina Syndrome 43 0.040
657
RPP001 Rapp-Hodgkin Syndrome 43 0.040
658
TST015 Testicular Disease 41 0.040
659
MYC017 Mycobacterium Kansasii 41 0.040
660
LYM105 Lymphoma, Follicular, Somatic 38 0.040
661
CYC007 Cyclic Thrombocytopenia 36 0.040
662
HMR023 Hemorrhagic Cystitis 35 0.040
663
INT038 Interdigitating Dendritic Cell Sarcoma 35 0.040
664
CHR020 Chronic Interstitial Cystitis 35 0.040
665
MYL013 Myeloperoxidase Deficiency 33 0.040
666
PLY010 Polyclonal Hypergammaglobulinemia 33 0.040
667
HPT012 Hepatocellular Fibrolamellar Carcinoma 27 0.040
668
PSL001 Pasli Disease 27 0.040
669
c DYS055 Dystonia 10 26 0.040
670
HYP179 Hypertrichosis Congenital Generalized X-Linked 26 0.040
671
MYL004 Myelodysplastic Myeloproliferative Cancer 24 0.040
672
GNR023 Generalized Eruptive Histiocytosis 22 0.040
673
BLD053 Blood Platelet Disease 21 0.040
674
ALD004 Ala Dehydratase Deficiency 12 0.040
675
P PRM021 Primary Pulmonary Hypertension 82 0.037
676
P OVR042 Ovarian Cancer 81 0.037
677
ACR007 Acromegaly 79 0.037
678
P MLR004 Malaria 75 0.037
679
SCK003 Sickle Cell Anemia 72 0.037
680
THR016 Thrombophlebitis 68 0.037
681
GNT003 Genital Herpes 68 0.037
682
P DRM010 Dermatomyositis 68 0.037
683
P MLG068 Malignant Glioma 68 0.037
684
GSG001 Gas Gangrene 67 0.037
685
P BLD042 Bladder Carcinoma 66 0.037
686
P PRT013 Portal Hypertension 66 0.037
687
PLS006 Plasmodium Vivax Malaria 65 0.037
688
P BRN019 Bernard-Soulier Syndrome 64 0.037
689
c MSC005 Muscular Dystrophy 62 0.037
690
P PRP025 Peripheral Primitive Neuroectodermal Tumor 62 0.037
691
CRY003 Cryptosporidiosis 62 0.037
692
c MTH007 Methemoglobinemia 62 0.037
693
GRY002 Gray Platelet Syndrome 60 0.037
694
TYP007 Typhoid Fever 60 0.037
695
c ATM011 Autoimmune Hepatitis 60 0.037
696
P GLC007 Glaucoma 60 0.037
697
P MMP001 Mumps 59 0.037
698
P CRT033 Corticobasal Degeneration 59 0.037
699
PPL002 Papillary Carcinoma 59 0.037
700
FLL008 Folliculitis 58 0.037
701
AMN001 Amenorrhea 57 0.037
702
LST001 Listeriosis 57 0.037
703
SDR002 Siderosis 56 0.037
704
ALP008 Alopecia 56 0.037
705
P HYP014 Hyperuricemia 56 0.037
706
HST009 Histiocytoma 55 0.037
707
RTN017 Retinal Detachment 55 0.037
708
FBR003 Fibrous Histiocytoma 54 0.037
709
BLS002 Blastomycosis 54 0.037
710
PTT004 Pituitary Apoplexy 54 0.037
711
c LTR001 Lateral Sclerosis 54 0.037
712
c LYM025 Lymphedema 53 0.037
713
HNT002 Hantavirus Pulmonary Syndrome 53 0.037
714
c OPH004 Ophthalmoplegia 53 0.037
715
TRP014 Triploidy 52 0.037
716
ORC001 Orchitis 52 0.037
717
c ACQ014 Acquired Hemophilia 52 0.037
718
c CNG027 Congenital Hemolytic Anemia 52 0.037
719
PRP034 Purpura Fulminans 52 0.037
720
PRP002 Periapical Granuloma 51 0.037
721
MNT147 Mental Retardation 51 0.037
722
FRZ001 Frozen Shoulder 51 0.037
723
CLC006 Calcinosis 51 0.037
724
OLG006 Oligoastrocytoma 50 0.037
725
MLK003 Melkersson-Rosenthal Syndrome 50 0.037
726
HYP068 Hyperostosis 50 0.037
727
c SML034 Small Cell Neuroendocrine Carcinoma 50 0.037
728
GST014 Gastrointestinal Lymphoma 49 0.037
729
SGT001 Sagittal Sinus Thrombosis 49 0.037
730
PDT021 Pediatric Osteosarcoma 48 0.037
731
CHY006 Chylous Ascites 48 0.037
732
PRP016 Paraplegia 47 0.037
733
PRG060 Pregnancy Loss 47 0.037
734
PLR008 Pleurisy 47 0.037
735
c DMY001 Demyelinating Polyneuropathy 46 0.037
736
PNH001 Panhypopituitarism 45 0.037
737
MCR017 Macrocytic Anemia 45 0.037
738
MLN057 Melanoma of Soft Parts 44 0.037
739
P PRM012 Primary Polycythemia 43 0.037
740
c CNG003 Congenital Dyserythropoietic Anemia 41 0.037
741
FBR002 Fibrosarcoma of Bone 41 0.037
742
c HRD086 Hereditary Hypophosphatemic Rickets 41 0.037
743
PRM014 Periampullary Adenocarcinoma 40 0.037
744
c CHR208 Chromosome 17p Deletion 40 0.037
745
HTL002 Htlv-1 Associated Myelopathy 39 0.037
746
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 38 0.037
747
MNN002 Mononeuritis Multiplex 38 0.037
748
PHH001 Phaeohyphomycosis 37 0.037
749
MSN004 Mesenchymal Cell Neoplasm 37 0.037
750
c HYD008 Hydrocephalus Due to Aqueductal Stenosis 36 0.037
751
BRT011 Bruton-Type Agammaglobulinemia 34 0.037
752
THY025 Thymus Cancer 32 0.037
753
MLG041 Malignant Triton Tumor 31 0.037
754
LNG004 Langerhans Cell Sarcoma 29 0.037
755
PRR008 Periarteritis Nodosa 28 0.037
756
ANP008 Anaplastic Oligoastrocytoma 28 0.037
757
IMM001 Immune-Complex Glomerulonephritis 28 0.037
758
RHB020 Rhabdomyosarcoma, Somatic 26 0.037
759
TRN028 Transient Acantholytic Dermatosis 26 0.037
760
NTR005 Nutritional Deficiency Disease 25 0.037
761
ORB012 Orbital Cancer 24 0.037
762
MYL049 Myelofibrosis, Somatic 24 0.037
763
c HRD133 Hereditary Aplastic Anemia 22 0.037
764
SML025 Small Non-Cleaved Cell Lymphoma 21 0.037
765
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 20 0.037
766
CYT018 Cytochrome P450 2d6 Variant 16 0.037
767
CDS001 Cadasil 84 0.034
768
P HRD008 Hereditary Hemorrhagic Telangiectasia 81 0.034
769
CLD001 Cleidocranial Dysplasia 77 0.034
770
P LPR003 Leprosy 77 0.034
771
CHD001 Chediak-Higashi Syndrome 75 0.034
772
LSH001 Leishmaniasis 74 0.034
773
KWS002 Kawasaki Disease 73 0.034
774
PRT036 Peritonitis 71 0.034
775
DBT011 Diabetic Retinopathy 70 0.034
776
CHR012 Chronic Granulomatous Disease 70 0.034
777
P LVR013 Liver Disease 69 0.034
778
CHR003 Cherubism 67 0.034
779
ALP001 Alopecia Universalis 67 0.034
780
PRP027 Peripheral Vascular Disease 67 0.034
781
P THR015 Thrombophilia 66 0.034
782
PBL001 Piebaldism 65 0.034
783
P LRY019 Laryngitis 65 0.034
784
P RHN004 Rhinitis 65 0.034
785
P RCK004 Rickets 64 0.034
786
P ALP009 Alopecia Areata 64 0.034
787
P HRD057 Hereditary Pancreatitis 64 0.034
788
P GRV001 Graves' Disease 64 0.034
789
PMS001 Poems Syndrome 63 0.034
790
c MCP010 Mucopolysaccharidosis 63 0.034
791
c INT070 Intestinal Obstruction 63 0.034
792
P KRT004 Keratitis 62 0.034
793
c THN001 Thanatophoric Dysplasia 61 0.034
794
HYD012 Hydrops Fetalis 61 0.034
795
GLS001 Gliosarcoma 61 0.034
796
VGT001 Vogt-Koyanagi-Harada Disease 60 0.034
797
DBL002 Double Outlet Right Ventricle 60 0.034
798
RBR001 Roberts Syndrome 60 0.034
799
P CRV035 Cervical Cancer 60 0.034
800
P ATY010 Atypical Hemolytic-Uremic Syndrome 59 0.034
801
ACR008 Acrocallosal Syndrome 59 0.034
802
SPN020 Spondylosis 59 0.034
803
CHR074 Choriocarcinoma 59 0.034
804
MLT001 Multiple Chemical Sensitivity 59 0.034
805
SLD003 Sialadenitis 59 0.034
806
c GLY013 Glycogen Storage Disease 59 0.034
807
INT051 Intussusception 58 0.034
808
TST014 Testicular Cancer 58 0.034
809
P CNG401 Congenital Heart Disease 58 0.034
810
c THR005 Thrombotic Thrombocytopenic Purpura 58 0.034
811
NNS005 Non-Small Cell Lung Carcinoma 58 0.034
812
P PLC011 Pilocytic Astrocytoma 57 0.034
813
ANR004 Anuria 57 0.034
814
CNG402 Congenital Insensitivity to Pain with Anhidrosis 57 0.034
815
CLS007 Classic Kaposi Sarcoma 57 0.034
816
c CTR002 Cataract 57 0.034
817
c XRD019 Xeroderma Pigmentosum, Group C 56 0.034
818
EXF001 Exfoliation Syndrome 56 0.034
819
PPL021 Papilledema 56 0.034
820
STV001 Stevens-Johnson Syndrome 55 0.034
821
ACR005 Acrodermatitis 55 0.034
822
P DWR001 Dwarfism 55 0.034
823
c XRD012 Xeroderma Pigmentosum, Group D 54 0.034
824
P INT064 Intermediate Uveitis 54 0.034
825
MYL001 Myelitis 54 0.034
826
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 54 0.034
827
P PRN022 Perineurioma 54 0.034
828
LMB002 Lambert-Eaton Myasthenic Syndrome 53 0.034
829
ACT008 Actinic Keratosis 53 0.034
830
VNS010 Venous Thromboembolism 53 0.034
831
c DFF019 Diffuse Gastric Cancer 53 0.034
832
PNM001 Pneumocystosis 53 0.034
833
PLM012 Pulmonary Sarcoidosis 53 0.034
834
PLY013 Polymyalgia Rheumatica 52 0.034
835
CYC004 Cyclic Hematopoiesis 52 0.034
836
NM001 Noma 52 0.034
837
RSD004 Rosai-Dorfman Disease 52 0.034
838
PTS001 Patau Syndrome 52 0.034
839
MMB002 Membranous Glomerulonephritis 51 0.034
840
GNG012 Gingival Overgrowth 51 0.034
841
INT075 Intracranial Hypertension 51 0.034
842
GNG005 Gangliocytoma 51 0.034
843
c DRR001 Diarrhea 51 0.034
844
P BRY001 Berylliosis 51 0.034
845
APP001 Apparent Mineralocorticoid Excess Syndrome 51 0.034
846
LPD004 Lipoid Nephrosis 51 0.034
847
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 51 0.034
848
STM007 Stomatitis 50 0.034
849
c ERY013 Erythrocytosis 50 0.034
850
CWP001 Cowpox 49 0.034
851
ASB001 Asbestosis 49 0.034
852
TXC002 Toxic Encephalopathy 49 0.034
853
PNV001 Panuveitis 48 0.034
854
CRB090 Cerebral Hypoxia 48 0.034
855
BLT006 Bilateral Breast Cancer 48 0.034
856
GNT031 Genitopatellar Syndrome 47 0.034
857
CRY001 Cryptogenic Organizing Pneumonia 47 0.034
858
GNG008 Ganglioneuroblastoma 46 0.034
859
DRM011 Dermatophytosis 46 0.034
860
MNN009 Meningoencephalitis 46 0.034
861
MCR037 Macroglossia 46 0.034
862
END021 Endomyocardial Fibrosis 46 0.034
863
P PLG001 Pelger-Huet Anomaly 46 0.034
864
MCP006 Mucoepidermoid Carcinoma 46 0.034
865
ECT026 Ectopic Pregnancy 45 0.034
866
ACT167 Acute Generalized Exanthematous Pustulosis 45 0.034
867
DFF024 Diffuse Panbronchiolitis 45 0.034
868
FSC004 Fasciitis 45 0.034
869
PRT038 Protein-Energy Malnutrition 45 0.034
870
ILS001 Ileus 44 0.034
871
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.034
872
BRS069 Breast Cancer, Somatic 43 0.034
873
SNL007 Senile Cataract 43 0.034
874
GND001 Gonadoblastoma 42 0.034
875
NWB001 Newborn Respiratory Distress Syndrome 41 0.034
876
P DCR003 Dacryoadenitis 41 0.034
877
5FL001 5-Fluorouracil Toxicity 41 0.034
878
ACL001 Acalculous Cholecystitis 40 0.034
879
c CHR253 Chromosome 5q Deletion 39 0.034
880
SBC024 Subcutaneous Panniculitis-Like T-Cell Lymphoma 39 0.034
881
P IRD006 Iridogoniodysgenesis, Dominant Type 38 0.034
882
ERY045 Erythrocytosis, Somatic 37 0.034
883
BNZ002 Benzene Toxicity 37 0.034
884
P SYS007 Systemic Capillary Leak Syndrome 37 0.034
885
P HYP071 Hypersensitivity Reaction Type Ii Disease 37 0.034
886
DST056 Distal 22q11.2 Microdeletion Syndrome 37 0.034
887
PRL008 Paralytic Ileus 36 0.034
888
ANM001 Anemia of Prematurity 35 0.034
889
GRN009 Granulomatous Hepatitis 35 0.034
890
ABL001 Ablepharon Macrostomia Syndrome 34 0.034
891
XLN009 X-Linked Spinal-Bulbar Muscle Atrophy 33 0.034
892
PLY021 Polyradiculopathy 33 0.034
893
CRV036 Cervical Carcinosarcoma 32 0.034
894
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 32 0.034
895
c CRN035 Cranial Nerve Palsy 31 0.034
896
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 31 0.034
897
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.034
898
c CNG023 Congenital Fibrosarcoma 30 0.034
899
DNG004 Dengue Fever, Protection Against 30 0.034
900
CRN061 Corneal Dystrophy Avellino Type 29 0.034
901
SPN066 Spinal-Bulbar Muscular Atrophy 27 0.034
902
DSC004 Discitis 25 0.034
903
BLN009 Balanoposthitis 24 0.034
904
PRD013 Periodic Fever, Familial, Autosomal Dominant 24 0.034
905
PL2001 Pla2g6-Associated Neurodegeneration 24 0.034
906
c MLG036 Malignant Spiradenoma 23 0.034
907
c RNG024 Ring Chromosome 8 23 0.034
908
CHR463 Chronic Actinic Dermatitis 22 0.034
909
P BKV001 Bk-Virus Nephropathy 22 0.034
910
VRS001 Virus Associated Hemophagocytic Syndrome 21 0.034
911
c TYP010 Type C Thymoma 21 0.034
912
DMD001 Demodicidosis 21 0.034
913
IND005 Indolent B Cell Lymphoma 21 0.034
914
CD3004 Cd3epsilon Deficiency 20 0.034
915
c CHR257 Chromosome 6q Deletion 19 0.034
916
MLT034 Multicystic Renal Dysplasia, Bilateral 19 0.034
917
RDT006 Radiation Induced Meningioma 19 0.034
918
PRK066 Parkinsonism with Spasticity, X-Linked 18 0.034
919
c TYP009 Type 2 Diabetes Mellitus 95 0.030
920
P TYP008 Type 1 Diabetes Mellitus 93 0.030
921
P AST005 Asthma 88 0.030
922
P FML011 Familial Adenomatous Polyposis 85 0.030
923
PHN003 Phenylketonuria 82 0.030
924
VNH001 Von Hippel-Lindau Disease 80 0.030
925
P WSK001 Wiskott-Aldrich Syndrome 78 0.030
926
FCT007 Factor Vii Deficiency 78 0.030
927
ACH004 Achondroplasia 78 0.030
928
INC002 Inclusion Body Myositis 77 0.030
929
P OST002 Osteoporosis 75 0.030
930
P CLC005 Celiac Disease 74 0.030
931
P ALX003 Alexander Disease 73 0.030
932
BRR003 Barrett's Esophagus 71 0.030
933
WRN001 Werner Syndrome 70 0.030
934
RLP001 Relapsing Polychondritis 70 0.030
935
CCC001 Coccidioidomycosis 70 0.030
936
PLY017 Polyarteritis Nodosa 69 0.030
937
CRY005 Cryptococcosis 68 0.030
938
PRT014 Protein S Deficiency 67 0.030
939
OMN001 Omenn Syndrome 66 0.030
940
P GST044 Gastritis 66 0.030
941
P TRN020 Turner Syndrome 66 0.030
942
DBN001 Dubin-Johnson Syndrome 64 0.030
943
PRL009 Prolactinoma 63 0.030
944
MXD005 Mixed Connective Tissue Disease 63 0.030
945
ISC004 Ischemia 63 0.030
946
P VLC001 Velocardiofacial Syndrome 63 0.030
947
LYM009 Lymphocytic Choriomeningitis 63 0.030
948
P RBL001 Rubella 62 0.030
949
CDL003 Caudal Regression Syndrome 62 0.030
950
KRN002 Kearns-Sayre Syndrome 61 0.030
951
GLD001 Goldenhar Syndrome 61 0.030
952
ALP007 Alpha 1-Antitrypsin Deficiency 61 0.030
953
LBR002 Leber Hereditary Optic Neuropathy 60 0.030
954
XLN001 X-Linked Ichthyosis 60 0.030
955
c LMB006 Limb-Girdle Muscular Dystrophy 60 0.030
956
P SYN007 Synovitis 59 0.030
957
VSC003 Visceral Leishmaniasis 59 0.030
958
P SCL015 Scleritis 59 0.030
959
P LRY016 Laryngeal Carcinoma 59 0.030
960
P PRM054 Primary Sclerosing Cholangitis 59 0.030
961
MCS003 Mucous Membrane Pemphigoid 58 0.030
962
ACR003 Acrodermatitis Enteropathica 58 0.030
963
ICH002 Ichthyosis Bullosa of Siemens 58 0.030
964
TBR011 Tuberculous Meningitis 58 0.030
965
P PPL020 Papillary Thyroid Carcinoma 58 0.030
966
CNN005 Connective Tissue Disease 58 0.030
967
c CNG124 Congenital Rubella 57 0.030
968
BRN029 Brain Disease 57 0.030
969
INT146 Intervertebral Disc Disease 57 0.030
970
P GNT008 Giant Cell Tumor 57 0.030
971
P HYP024 Hypoparathyroidism 57 0.030
972
SPN051 Spondylitis 57 0.030
973
RBS001 Rabies 57 0.030
974
SCN006 Secondary Syphilis 57 0.030
975
c ANG015 Angioedema 57 0.030
976
ACN011 Acne 57 0.030
977
P MTB001 Metabolic Syndrome X 56 0.030
978
NDL013 Nodular Regenerative Hyperplasia 56 0.030
979
DDN006 Duodenitis 56 0.030
980
TTH006 Tooth Disease 55 0.030
981
INS008 Insulin-Like Growth Factor I Deficiency 55 0.030
982
c HRD001 Hereditary Multiple Exostoses 55 0.030
983
c BRG001 Brugada Syndrome 55 0.030
984
PRT018 Portal Vein Thrombosis 54 0.030
985
c LPR012 Leopard Syndrome 1 54 0.030
986
DBT006 Diabetic Macular Edema 54 0.030
987
FLL013 Follicular Dendritic Cell Sarcoma 54 0.030
988
PTT037 Pituitary Tumors 54 0.030
989
ANH002 Anhidrosis 54 0.030
990
HLL004 Hellp Syndrome 54 0.030
991
TNG003 Tongue Cancer 53 0.030
992
P CHR019 Choroid Plexus Carcinoma 53 0.030
993
BRN004 Brain Edema 53 0.030
994
P INT072 Intestinal Pseudo-Obstruction 53 0.030
995
ATY008 Atypical Lipomatous Tumor 53 0.030
996
SPR010 Sporotrichosis 52 0.030
997
P CNT005 Central Nervous System Lymphoma 52 0.030
998
LPS007 Lupus Nephritis 52 0.030
999
IGG001 Iga Glomerulonephritis 52 0.030
1000
EMP001 Empty Sella Syndrome 52 0.030
1001
c HPT007 Hepatitis E 52 0.030
1002
P PST022 Posterior Uveal Melanoma 51 0.030
1003
GLS007 Glossitis 51 0.030
1004
JVN033 Juvenile Nasopharyngeal Angiofibroma 51 0.030
1005
c FML024 Familial Melanoma 51 0.030
1006
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 51 0.030
1007
ADN014 Adenomatoid Tumor 51 0.030
1008
HMR002 Hemarthrosis 51 0.030
1009
c ANT034 Anterior Uveitis 51 0.030
1010
P CYS018 Cystitis 51 0.030
1011
WBR001 Weber Syndrome 51 0.030
1012
c KRT005 Keratoacanthoma 51 0.030
1013
P CST002 Castleman's Disease 50 0.030
1014
PRT019 Protein-Losing Enteropathy 50 0.030
1015
c ATM024 Autoimmune Pancreatitis 50 0.030
1016
BRN018 Borna Disease 50 0.030
1017
GST060 Gastric Cancer, Somatic 50 0.030
1018
FBR009 Fibrous Dysplasia 50 0.030
1019
ANL011 Anal Canal Carcinoma 50 0.030
1020
SPN032 Spindle Cell Carcinoma 49 0.030
1021
OPT009 Optic Neuritis 49 0.030
1022
ERY017 Erythema Elevatum Diutinum 49 0.030
1023
FCT005 Factor Xiii Deficiency 49 0.030
1024
P CLL015 Collagen Disease 49 0.030
1025
CNV002 Conversion Disorder 49 0.030
1026
MLT075 Multifocal Motor Neuropathy 49 0.030
1027
INF058 Inflammatory Myofibroblastic Tumor 48 0.030
1028
RTN003 Retinal Ischemia 48 0.030
1029
NPH003 Nephrocalcinosis 48 0.030
1030
MDT001 Mediterranean Spotted Fever 48 0.030
1031
NRT004 Neuritis 48 0.030
1032
IMM060 Immunodeficiency, Common Variable, 9 48 0.030
1033
CMM014 Common Variable Immune Deficiency 47 0.030
1034
c CHR048 Chronic Rhinitis 47 0.030
1035
CD4002 Cd40 Deficiency 47 0.030
1036
c ATM019 Autoimmune Polyendocrine Syndrome 46 0.030
1037
CRY021 Cryoglobulinemic Vasculitis 46 0.030
1038
CNT025 Central Pontine Myelinolysis 46 0.030
1039
TNS001 Tenosynovial Giant Cell Tumor 46 0.030
1040
STC004 Stachybotrys Chartarum 46 0.030
1041
PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 45 0.030
1042
BWN003 Bowenoid Papulosis 45 0.030
1043
GMM002 Gamma Chain Deficiency 45 0.030
1044
c ART084 Arteriovenous Fistula 45 0.030
1045
MXL004 Maxillary Sinus Squamous Cell Carcinoma 45 0.030
1046
MLG121 Male Germ Cell Tumor, Somatic 45 0.030
1047
INT067 Interstitial Nephritis 45 0.030
1048
NRL007 Neurologic Diseases 45 0.030
1049
INF034 Infective Endocarditis 45 0.030
1050
UNL002 Unilateral Retinoblastoma 44 0.030
1051
c TRC005 Tracheal Stenosis 44 0.030
1052
SPR005 Superficial Basal Cell Carcinoma 44 0.030
1053
FST010 Fasting Hypoglycemia 44 0.030
1054
FML055 Familial Cylindromatosis 44 0.030
1055
NCR007 Necrotizing Fasciitis 44 0.030
1056
QDR001 Quadriplegia 43 0.030
1057
DYS101 Dysgerminoma 43 0.030
1058
TRT001 Teratocarcinoma 43 0.030
1059
MYC019 Mycobacterium Marinum 43 0.030
1060
CND006 Candida Glabrata 43 0.030
1061
THY043 Thymic Hyperplasia 43 0.030
1062
NPH017 Nephrosis 42 0.030
1063
P BRS044 Breast Adenocarcinoma 42 0.030
1064
CNJ012 Conjunctival Disease 41 0.030
1065
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 40 0.030
1066
PLS009 Plasma Cell Neoplasm 40 0.030
1067
GNG006 Gingival Hypertrophy 40 0.030
1068
INP001 Inappropriate Adh Syndrome 40 0.030
1069
GST040 Gastric Adenocarcinoma 40 0.030
1070
c HVY001 Heavy Chain Disease 39 0.030
1071
ENT007 Enteropathica 39 0.030
1072
WRN003 Wernicke Encephalopathy 39 0.030
1073
PTY004 Pityriasis Lichenoides 39 0.030
1074
GST012 Gastroesophageal Junction Adenocarcinoma 38 0.030
1075
c MLR021 Malaria, Severe 38 0.030
1076
c ACQ012 Acquired Angioedema 38 0.030
1077
P OTT001 Otitis Externa 38 0.030
1078
CHL056 Cheilitis 38 0.030
1079
P GMM003 Gamma Heavy Chain Disease 37 0.030
1080
RTN013 Retinal Hemangioblastoma 37 0.030
1081
FTD001 Foot Drop 37 0.030
1082
TST004 Testicular Lymphoma 36 0.030
1083
CMB021 Combined Pituitary Hormone Deficiency 36 0.030
1084
TLS001 Tolosa-Hunt Syndrome 36 0.030
1085
P RNG004 Ring Chromosome 1 36 0.030
1086
HPT063 Hepatitis B Virus Infection 36 0.030
1087
GTT002 Guttate Psoriasis 36 0.030
1088
PTT021 Pituitary Hormone Deficiency, Combined 2 35 0.030
1089
CHR415 Chronic Venous Leg Ulcers 35 0.030
1090
BRC011 Brachial Plexus Neuropathy 34 0.030
1091
SZR001 Sezary's Disease 34 0.030
1092
KLD001 Keloids 34 0.030
1093
BLD087 Bladder Cancer, Somatic 34 0.030
1094
NCR009 Necrobiotic Xanthogranuloma 34 0.030
1095
DYS012 Dyshidrosis 34 0.030
1096
PLM074 Pulmonary Function 34 0.030
1097
NDL020 Nodal Marginal Zone B-Cell Lymphoma 33 0.030
1098
ENG004 Engraftment Syndrome 33 0.030
1099
c RHB009 Rhabdomyosarcoma 2, Alveolar 32 0.030
1100
TRC006 Trichosporonosis 32 0.030
1101
PRS108 Persistent Polyclonal B-Cell Lymphocytosis 32 0.030
1102
EPD018 Epididymo-Orchitis 31 0.030
1103
BRG002 Berger Disease 31 0.030
1104
CHL040 Cholangiolocellular Carcinoma 31 0.030
1105
TST021 Testicular Germ Cell Tumor 31 0.030
1106
c CHR091 Chronic Meningitis 31 0.030
1107
NCR001 Necrotizing Ulcerative Gingivitis 30 0.030
1108
c ACQ010 Acquired Polycythemia 29 0.030
1109
c RNG022 Ring Chromosome 6 29 0.030
1110
P PLM064 Pulmonary Sequestration 29 0.030
1111
c CHR193 Chromosome 13q Deletion 28 0.030
1112
CNG028 Congenital Hypoplastic Anemia 27 0.030
1113
LCH007 Lichen Planus Follicularis 27 0.030
1114
c ATX026 Ataxia-Telangiectasia Variant 27 0.030
1115
MYL015 Myeloproliferative Disorder with Eosinophilia 25 0.030
1116
CRT009 Critical Illness Polyneuropathy 24 0.030
1117
SFM001 Sfm Syndrome, Somatic Mosaic 23 0.030
1118
ANG022 Angel Shaped Phalangoepiphyseal Dysplasia 23 0.030
1119
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 21 0.030
1120
RFR009 Refractory Cytopenia with Multilineage Dysplasia 21 0.030
1121
SPL009 Splenic Sequestration 21 0.030
1122
EXT039 Extrapontine Myelinolysis 20 0.030
1123
SCL008 Scleromalacia Perforans 20 0.030
1124
GRW021 Growing Teratoma Syndrome 20 0.030
1125
IND009 Indeterminate Cell Histiocytosis 20 0.030
1126
GRN011 Granulomatous Gastritis 19 0.030
1127
ANP010 Anaplastic Plasmacytoma 18 0.030
1128
EMB015 Embryonal Tumor with Multilayered Rosettes 18 0.030
1129
GRN021 Granulomatous Rosacea 17 0.030
1130
INF127 Infective Dermatitis Associated with Htlv-1 17 0.030
1131
EPS031 Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma of the Elderly 17 0.030
1132
c RNG021 Ring Chromosome 5 16 0.030
1133
BCL003 B-Cell Lymphocytic Neoplasm 16 0.030
1134
HHV001 Hhv-6 Encephalitis 16 0.030
1135
c CLR075 Colorectal Cancer 3 14 0.030
1136
ASP009 Aspergillus Niger Infection 13 0.030
1137
MDS024 Mediastinal Endodermal Sinus Tumors 13 0.030
1138
c VRL008 Viral Exanthem 13 0.030
1139
c PSD024 Pseudo Pelger-Huet Anomaly 11 0.030
1140
CYS001 Cystic Fibrosis 96 0.026
1141
P PNC035 Pancreatic Cancer 91 0.026
1142
P TBR001 Tuberous Sclerosis 85 0.026
1143
P SCH015 Schizophrenia 82 0.026
1144
P NMN002 Niemann-Pick Disease 81 0.026
1145
P RTN008 Retinitis Pigmentosa 80 0.026
1146
CNG034 Congestive Heart Failure 78 0.026
1147
WLS001 Wilson Disease 77 0.026
1148
ACT033 Acute Intermittent Porphyria 76 0.026
1149
LRN002 Laron Syndrome 76 0.026
1150
CYS013 Cystinuria 75 0.026
1151
P MLT007 Multiple Epiphyseal Dysplasia 73 0.026
1152
MNK001 Menkes Disease 73 0.026
1153
CFF002 Coffin-Lowry Syndrome 72 0.026
1154
P BRD002 Bardet-Biedl Syndrome 71 0.026
1155
RNL002 Renal Agenesis 70 0.026
1156
ART016 Aortic Aneurysm 70 0.026
1157
P MLT042 Multiple Endocrine Neoplasia Type 2a 70 0.026
1158
WRM001 Wermer Syndrome 69 0.026
1159
P END044 Endometriosis 69 0.026
1160
BLL006 Bullous Pemphigoid 69 0.026
1161
BRN024 Bronchitis 69 0.026
1162
P MRT001 Muir-Torre Syndrome 68 0.026
1163
DSM004 Desmoid Tumor 67 0.026
1164
LMY002 Leiomyoma 67 0.026
1165
GST023 Gastric Ulcer 67 0.026
1166
TRG002 Trigeminal Neuralgia 67 0.026
1167
P DGR001 Digeorge Syndrome 67 0.026
1168
PRT002 Paratyphoid Fever 66 0.026
1169
MCK007 Muckle-Wells Syndrome 66 0.026
1170
P PRD008 Periodontitis 66 0.026
1171
P ANR007 Anorexia Nervosa 66 0.026
1172
ALS001 Alstrom Syndrome 66 0.026
1173
OLL001 Ollier Disease 66 0.026
1174
EXT034 Extrinsic Allergic Alveolitis 65 0.026
1175
c TXP001 Toxoplasmosis 65 0.026
1176
MLB002 Male Breast Cancer 65 0.026
1177
PHR003 Pharyngitis 65 0.026
1178
DBT001 Diabetic Ketoacidosis 65 0.026
1179
c LNG028 Long Qt Syndrome 64 0.026
1180
c SCL016 Scleroderma 64 0.026
1181
STR067 Stroke, Ischemic 64 0.026
1182
CRB039 Cerebrovascular Disease 64 0.026
1183
P SLV001 Silver-Russell Syndrome 64 0.026
1184
HMH002 Hemihypertrophy 64 0.026
1185
P VRL007 Viral Encephalitis 64 0.026
1186
P DRM007 Dermatitis Herpetiformis 64 0.026
1187
P BSL007 Basal Cell Carcinoma 63 0.026
1188
FCT003 Factor X Deficiency 63 0.026
1189
P OST001 Osteopetrosis 63 0.026
1190
PTT006 Pituitary Adenoma 63 0.026
1191
EPD006 Epidermolysis Bullosa Acquisita 63 0.026
1192
TTN003 Tetanus 63 0.026
1193
CRN036 Craniopharyngioma 63 0.026
1194
CHG001 Chagas Disease 62 0.026
1195
WLL006 Wells Syndrome 62 0.026
1196
c TMP001 Temporal Lobe Epilepsy 62