Search results for "leukemia"

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

2325 hits were found for 'leukemia'

# Family MCID Name MIFTS Score
1
c MYL006 Myeloid Leukemia 75 7.637
2
P LKM002 Leukemia 77 7.436
3
P CHR090 Chronic Lymphocytic Leukemia 89 6.526
4
c CHR065 Chronic Myeloid Leukemia 73 5.815
5
P ACT019 Acute Myeloid Leukemia 93 5.460
6
ACT095 Acute Biphenotypic Leukemia 55 4.745
7
ACT119 Acute Promyelocytic Leukemia 68 4.616
8
P ACT101 Acute Lymphoblastic Leukemia 63 4.582
9
P JVN004 Juvenile Myelomonocytic Leukemia 70 4.102
10
MGK001 Megakaryocytic Leukemia 57 4.101
11
P ACT020 Acute T Cell Leukemia 41 4.094
12
c ACT073 Acute Leukemia 57 4.021
13
NTR003 Natural Killer Cell Leukemia 57 3.889
14
P ACT009 Acute Monocytic Leukemia 57 3.825
15
c ADL017 Adult T-Cell Leukemia 46 3.685
16
c ACT115 Acute Myeloid Leukemia, Adult 55 3.679
17
c LYM026 Lymphoblastic Leukemia 57 3.638
18
c TCL004 T-Cell Leukemia 51 3.507
19
HRY003 Hairy Cell Leukemia 59 3.447
20
c ACT074 Acute Lymphocytic Leukemia 70 3.409
21
c CHR285 Chronic Myelomonocytic Leukemia 56 3.315
22
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 3.287
23
ACT098 Acute Erythroid Leukemia 43 3.217
24
c ACT117 Acute Myelomonocytic Leukemia 55 3.187
25
c MNC007 Monocytic Leukemia 57 3.153
26
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 21 3.006
27
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 12 2.945
28
c ADL052 Adult Acute Lymphocytic Leukemia 54 2.923
29
LRG008 Large Granular Lymphocyte Leukemia 40 2.920
30
ACT200 Acute Monoblastic Leukemia 47 2.890
31
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 46 2.831
32
PRL017 Prolymphocytic Leukemia 44 2.800
33
c LKM060 Leukemia, Acute Lymphoblastic 3 48 2.799
34
PLS016 Plasma Cell Leukemia 49 2.799
35
c SBC004 Subacute Myeloid Leukemia 22 2.774
36
CHL061 Childhood Leukemia 39 2.730
37
CNT018 Central Nervous System Leukemia 41 2.728
38
P BCL005 B Cell Prolymphocytic Leukemia 25 2.658
39
c LKM005 Leukemia, T-Cell, Chronic 17 2.617
40
c TCL005 T-Cell Prolymphocytic Leukemia 49 2.598
41
CHR286 Chronic Neutrophilic Leukemia 49 2.581
42
ACT103 Acute Lymphoblastic Leukemia, Childhood 15 2.562
43
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 14 2.562
44
NNN018 Noonan-Like Syndrome Disorder with or Without Juvenile Myelomonocytic Leukemia 21 2.529
45
c SYS004 Systemic Mastocytosis 59 2.482
46
SBL003 Subleukemic Leukemia 13 2.360
47
HCL001 Hcl-V 30 2.345
48
LYM067 Lymphoid Leukemia 42 2.322
49
P PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 11 2.310
50
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 29 2.285
51
CRB138 Core Binding Factor Acute Myeloid Leukemia 47 2.255
52
TST003 Testicular Leukemia 20 2.173
53
ACT113 Acute Myeloblastic Leukemia with Maturation 34 2.135
54
c CHR064 Chronic Monocytic Leukemia 22 2.128
55
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 2.120
56
NLL001 Null-Cell Leukemia 10 2.085
57
c LKM004 Leukemia, B-Cell, Chronic 15 2.080
58
P TCL001 T-Cell Adult Acute Lymphocytic Leukemia 8 2.060
59
PRG005 Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 7 2.060
60
PST004 Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 7 2.060
61
c HMN021 Human T-Cell Leukemia Virus Type 1 41 2.049
62
MST002 Mast-Cell Leukemia 35 1.997
63
ACT118 Acute Non Lymphoblastic Leukemia 24 1.989
64
c CHR418 Chronic Leukemia 37 1.974
65
ALK003 Aleukemic Leukemia Cutis 20 1.947
66
ACT177 Acute Basophilic Leukemia 38 1.945
67
P PRB001 Pre-B-Cell Acute Lymphoblastic Leukemia 40 1.927
68
P LFR001 Li-Fraumeni Syndrome 88 1.899
69
RFR002 Refractory Hairy Cell Leukemia 14 1.873
70
ACT097 Acute Erythroblastic Leukemia 12 1.873
71
NNT007 Neonatal Leukemia 22 1.860
72
c SBC006 Subacute Leukemia 13 1.836
73
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 12 1.822
74
LKM036 Leukemia, Acute Nonlymphocytic 10 1.817
75
ALK002 Aleukemic Monocytic Leukemia Cutis 9 1.817
76
FML083 Familial Platelet Disorder with Associated Myeloid Malignancy 24 1.812
77
c SBC015 Subacute Monocytic Leukemia 13 1.812
78
PLS003 Plasmacytic Leukemia 12 1.806
79
SPL013 Splenic Manifestation of Leukemia 7 1.799
80
PDT026 Pediatric T-Cell Leukemia 3 1.799
81
c INH015 Inherited Acute Myeloid Leukemia 14 1.784
82
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 8 1.784
83
PRC009 Precursor T-Lymphoblastic Lymphoma/leukemia Refractory 7 1.784
84
CHL029 Childhood Precursor T-Lymphoblastic Lymphoma/leukemia 5 1.784
85
c PRC017 Precursor Lymphoblastic Lymphoma/leukemia 5 1.784
86
P FML096 Familial Acute Myelocytic Leukemia 4 1.784
87
SPL002 Splenic Manifestation of Prolymphocytic Leukemia 4 1.784
88
SPL010 Splenic Manifestation of Hairy Cell Leukemia 4 1.784
89
c HMN022 Human T-Cell Leukemia Virus Type 2 40 1.616
90
c FML114 Familial Chronic Lymphocytic Leukemia 38 1.600
91
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 27 1.549
92
c 8P1002 8p11 Myeloproliferative Syndrome 38 1.538
93
CLL014 Cll/sll 30 1.538
94
MYL050 Myeloid Leukemia, Acute, M4/m4eo Subtype, Somatic 36 1.531
95
P ACT208 'acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation' 30 1.531
96
LKM016 Leukemia, Acute Myeloid, Somatic 36 1.527
97
LKM017 Leukemia, Acute Myeloid, Reduced Survival in 36 1.527
98
ACT178 Acute Myeloid Leukemia with Multilineage Dysplasia 20 1.527
99
ACT207 'acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)' 30 1.514
100
TCL015 T-Cell Acute Lymphoblastic Leukemia, Somatic 23 1.514
101
ALK014 Aleukemic Mast Cell Leukemia 13 1.509
102
c ACT203 'acute Myeloid Leukemia with T(9;11)(p22;q23)' 19 1.504
103
c ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 20 1.499
104
LKM058 Leukemia, Acute Lymphoblastic, Somatic 14 1.499
105
c FML095 Familial Acute Lymphocytic Leukemia 10 1.499
106
c ACT106 Acute Myeloblastic Leukemia Type 1 6 1.499
107
c ACT107 Acute Myeloblastic Leukemia Type 2 6 1.499
108
P ACT108 Acute Myeloblastic Leukemia Type 3 6 1.499
109
c ACT110 Acute Myeloblastic Leukemia Type 5 6 1.499
110
c ACT111 Acute Myeloblastic Leukemia Type 6 6 1.499
111
c ACT112 Acute Myeloblastic Leukemia Type 7 6 1.499
112
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 17 1.494
113
c ACT109 Acute Myeloblastic Leukemia Type 4 5 1.494
114
c ACT205 'acute Myeloid Leukemia with T(6;9)(p23;q34)' 12 1.488
115
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 11 1.488
116
P LKM024 Leukemia/lymphoma, T-Cell 11 1.482
117
BLN016 Bilineal Acute Leukemia 10 1.482
118
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 8 1.482
119
c HMN023 Human T-Cell Leukemia Virus Type 3 8 1.482
120
ACT116 Acute Myeloid Leukemia, Childhood 4 1.482
121
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 5 1.474
122
c MYL018 Myelocytic Leukemia-Like Syndrome, Familial, Chronic 4 1.474
123
MGK006 'megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13)' 9 1.466
124
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 8 1.466
125
c FML115 Familial Chronic Myelocytic Leukemia 5 1.466
126
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 2 1.466
127
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 11 1.457
128
c LKM008 Leukemia, Acute Pre-B-Cell 11 1.457
129
c NPM001 Npm1-Related Acute Myeloid Leukemia 10 1.457
130
HRY001 Hairy Cell Leukemia of Spleen 10 1.457
131
LKM026 Leukemia, Acute Myeloid, Therapy-Related 8 1.457
132
c LKM050 Leukemia, Chronic Lymphocytic 1 8 1.457
133
c LKM051 Leukemia, Chronic Lymphocytic 3 8 1.457
134
c LKM052 Leukemia, Chronic Lymphocytic 5 8 1.457
135
c LKM053 Leukemia, Chronic Lymphocytic 4 8 1.457
136
c LKM054 Leukemia, Acute Lymphocytic 1 8 1.457
137
c LKM056 Leukemia, Chronic Lymphocytic 2 8 1.457
138
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 8 1.457
139
LKM023 Leukemia, Myeloid/lymphoid or Mixed-Lineage 7 1.457
140
c LKM055 Leukemia, Acute Lymphoblastic 2 7 1.457
141
c LYM061 Lymphocytic Leukemia, Acute T-Cell 7 1.457
142
ACT204 'acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2)' 7 1.457
143
c LKM009 Leukemia/lymphoma, B-Cell, 2 6 1.457
144
c LKM010 Leukemia/lymphoma, B-Cell, 3 6 1.457
145
LKM018 Leukemia, T-Cell Acute Lymphoblastoid 6 1.457
146
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 6 1.457
147
BND002 B- and T-Cell Mixed Leukemia 6 1.457
148
CLS019 Classic Mast Cell Leukemia 6 1.457
149
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 5 1.457
150
LKM020 Leukemia, Acute Myeloid, with Eosinophilia 5 1.457
151
TCL013 T-Cell Prolymphocytic Leukemia, Somatic 5 1.457
152
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 5 1.457
153
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 5 1.457
154
LKM019 Leukemia, Philadelphia Chromosome-Positive, Resistant to Imatinib 4 1.457
155
LKM022 Leukemia, Acute Promyelocytic, Pml/rara Type 4 1.457
156
LKM035 Leukemia, Acute Promyelocytic, Stat5b/rara Type 4 1.457
157
LKM037 Leukemia, Acute Promyelocytic, Numa/rara Type 4 1.457
158
LKM038 Leukemia, Acute Promyelocytic, Npm/rara Type 4 1.457
159
LKM039 Leukemia, Acute Promyelocytic, Pl2f/rara Type 4 1.457
160
LKM057 Leukemia, Post-Chemotherapy 4 1.457
161
c LYM062 Lymphoma/leukemia, B-Cell, Variant 4 1.457
162
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 4 1.457
163
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 4 1.457
164
LKM034 Leukemia, Transient, of Down Syndrome 3 1.457
165
AZT002 Azathioprine Dose Selection in the Treatment of Crohn Disease, Leukemia and in Transplantation 2 1.457
166
MRC007 Mercaptopurine Dose Selection in the Treatment of Crohn Disease, Leukemia and in Transplantation 2 1.457
167
LYM040 Lymphoblastic Lymphoma 54 1.316
168
P HYP098 Hypereosinophilic Syndrome 62 1.199
169
P FML045 Familial Mosaic Monosomy 7 Syndrome 17 1.104
170
EMB016 Emberger Syndrome 26 1.080
171
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 22 1.080
172
NSY001 N Syndrome 33 1.043
173
WTL001 Wt Limb Blood Syndrome 23 1.030
174
MYL040 Myelodysplastic Syndromes 81 0.308
175
HMT018 Hematopoietic Stem Cell Transplantation 41 0.220
176
c MYL007 Myeloma 61 0.194
177
SRC014 Sarcoma 70 0.187
178
END072 Endotheliitis 51 0.169
179
P MLT019 Multiple Myeloma 88 0.164
180
DWN001 Down Syndrome 62 0.151
181
P GRF002 Graft Versus Host Disease 65 0.150
182
P MYL005 Myelofibrosis 75 0.147
183
P WLM002 Wilms Tumor 66 0.142
184
HDG007 Hodgkin's Lymphoma 93 0.140
185
c NTR004 Neutropenia 64 0.138
186
THR013 Thoracic Outlet Syndrome 52 0.137
187
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.136
188
P BCL006 B-Cell Lymphomas 57 0.133
189
c HPT021 Hepatitis 64 0.132
190
P MST009 Mastocytosis 75 0.131
191
SYN053 Syndromic Diarrhea 34 0.131
192
MYL003 Myeloid Sarcoma 56 0.130
193
LYM019 Lymphosarcoma 59 0.129
194
P BRS047 Breast Cancer 86 0.126
195
c HML002 Hemolytic Anemia 66 0.125
196
HYP004 Hypercalcemia 65 0.124
197
P ESN007 Eosinophilia 63 0.123
198
RFR010 Refractory Anemia 50 0.121
199
BRK003 Burkitt's Lymphoma 77 0.120
200
NNH001 Non-Hodgkin Lymphoma 73 0.120
201
P ATX002 Ataxia Telangiectasia 87 0.116
202
P HST010 Histiocytosis 64 0.116
203
ANK002 Ankylosing Spondylitis 77 0.113
204
P ATM010 Autoimmune Hemolytic Anemia 62 0.113
205
c BNG076 Benign Exophthalmos Syndrome 22 0.112
206
P ANG001 Angelman Syndrome 70 0.111
207
ART019 Aortic Valve Stenosis 64 0.111
208
P RHM011 Rheumatoid Arthritis 94 0.110
209
ACN002 Acanthosis Nigricans 63 0.110
210
P ATX010 Ataxia Neuropathy Spectrum 43 0.109
211
P ART022 Arthritis 75 0.108
212
P APL001 Aplastic Anemia 83 0.104
213
c THR014 Thrombocytopenia 71 0.104
214
PRS047 Prostatitis 60 0.104
215
SVR004 Severe Combined Immunodeficiency 74 0.103
216
c MNN013 Meningitis 68 0.103
217
c PLY018 Polycythemia 59 0.103
218
PRR002 Pure Red-Cell Aplasia 56 0.103
219
PLY001 Polycythemia Vera 85 0.102
220
c ESS003 Essential Thrombocythemia 61 0.102
221
RCH001 Richter's Syndrome 36 0.102
222
ASP006 Aspergillosis 73 0.101
223
DSS009 Disseminated Intravascular Coagulation 62 0.101
224
LKS001 Leukostasis 50 0.101
225
P PNM007 Pneumonia 78 0.100
226
BNM005 Bone Marrow Necrosis 39 0.100
227
P NRF002 Neurofibromatosis 94 0.098
228
VSC011 Vasculitis 66 0.098
229
c THY032 Thyroiditis 66 0.096
230
SPS019 Spastic Paraparesis 41 0.096
231
SPS057 Spasticity 38 0.096
232
MNT001 Mantle Cell Lymphoma 64 0.095
233
c HMP002 Hemophagocytic Lymphohistiocytosis 60 0.095
234
AND002 Androgen Insensitivity Syndrome 80 0.094
235
c AXN002 Axenfeld-Rieger Syndrome 67 0.094
236
THR004 Thrombocytosis 61 0.094
237
CRB009 Cerebritis 39 0.094
238
GLC037 Glucocorticoid Resistance 51 0.093
239
MCR004 Macroglobulinemia 55 0.091
240
TRP002 Tropical Spastic Paraparesis 55 0.091
241
c NNN003 Noonan Syndrome 80 0.090
242
TTR011 Tetraploidy 61 0.090
243
RTN023 Retinitis 54 0.090
244
P LVR011 Liver Cancer 91 0.089
245
NRP001 Neuropathy 62 0.089
246
P FNC001 Fanconi's Anemia 67 0.088
247
ART001 Arterial Tortuosity Syndrome 55 0.088
248
AND003 Andersen-Tawil Syndrome 54 0.088
249
LKM001 Leukemoid Reaction 49 0.088
250
P RTN024 Retinoblastoma 82 0.086
251
c MLG054 Malignant Histiocytosis 63 0.086
252
DPH001 Diphtheria 58 0.086
253
P SVR003 Severe Congenital Neutropenia 53 0.086
254
MDS022 Mediastinitis 46 0.085
255
TFT003 Tufting Enteropathy 28 0.085
256
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.085
257
c ATX004 Ataxia 59 0.084
258
P DBT005 Diabetes Insipidus 58 0.084
259
BCT015 Bacteremia 50 0.084
260
P PNC001 Pancytopenia 48 0.084
261
P MLN008 Melanoma 65 0.082
262
c ACT135 Acute Graft Versus Host Disease 49 0.082
263
PRP030 Purpura 66 0.081
264
c ACR001 Aicardi-Goutieres Syndrome 54 0.079
265
P LNG032 Lung Cancer 79 0.078
266
HMT002 Hematologic Cancer 63 0.078
267
HYP266 Hypoxia 58 0.078
268
SMT015 Smith Magenis Syndrome 57 0.078
269
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 54 0.078
270
P PRS040 Prostate Cancer 98 0.077
271
P GLM007 Glomerulonephritis 69 0.077
272
LNG024 Langerhans-Cell Histiocytosis 57 0.077
273
GRN017 Granulocytopenia 47 0.077
274
c CHR417 Chronic Graft Versus Host Disease 43 0.077
275
P MLT020 Multiple Sclerosis 85 0.075
276
P NRB001 Neuroblastoma 70 0.075
277
c PNC044 Pancreatitis 69 0.075
278
P INF038 Influenza 68 0.075
279
GNG013 Gingivitis 61 0.075
280
DFF005 Diffuse Large B-Cell Lymphoma 56 0.075
281
HMG002 Hemoglobinuria 52 0.075
282
SPL018 Splenomegaly 47 0.075
283
BLS007 Blastic Plasmacytoid Dendritic Cell 45 0.075
284
CHR066 Chronic Fatigue Syndrome 66 0.074
285
MYC002 Mycobacterium Avium Complex Disease 59 0.074
286
HST016 Histiocytic Sarcoma 52 0.074
287
ZYG002 Zygomycosis 45 0.074
288
HV1006 Hiv-1 64 0.072
289
P ADN016 Adenocarcinoma 59 0.072
290
INV001 Invasive Aspergillosis 53 0.072
291
EMN001 Emanuel Syndrome 37 0.072
292
ADS002 Adie Syndrome 35 0.072
293
HNM002 Hinman Syndrome 28 0.072
294
HYP084 Hypopyon 25 0.072
295
AND005 Androgen Insensitivity Syndrome, Mild 21 0.072
296
P OBS005 Obesity 91 0.070
297
P HYP075 Hypertension 87 0.070
298
MYC006 Mycosis Fungoides 69 0.070
299
P HRP006 Herpes Simplex 68 0.070
300
P CND004 Candidiasis 62 0.070
301
P PLY019 Polyneuropathy 61 0.070
302
P PLM006 Pulmonary Alveolar Proteinosis 53 0.070
303
c CNT035 Central Nervous System Disease 49 0.070
304
c HPT016 Hepatitis B 70 0.069
305
ABT001 Abetalipoproteinemia 65 0.069
306
P ANP001 Anaplastic Large Cell Lymphoma 63 0.069
307
OST003 Osteonecrosis 59 0.069
308
BNM001 Bone Marrow Cancer 54 0.069
309
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.069
310
IPX001 Ipex Syndrome 37 0.069
311
TBR010 Tuberculosis 87 0.067
312
P SRC013 Sarcoidosis 75 0.067
313
SPS077 Sepsis 70 0.067
314
P NJM001 Nijmegen Breakage Syndrome 70 0.067
315
P HPT001 Hepatitis C 67 0.067
316
DRM006 Dermatitis 66 0.067
317
URT039 Urticaria 64 0.067
318
NRN002 Neuronitis 44 0.067
319
P MNN012 Meningioma 78 0.065
320
MGL001 Megaloblastic Anemia 66 0.065
321
DFC004 Deficiency Anemia 63 0.065
322
c PRP029 Porphyria 63 0.065
323
P THR090 Thrombocythemia 1 58 0.065
324
HRP004 Herpes Zoster 58 0.065
325
HPT023 Hepatocellular Carcinoma 54 0.065
326
CTN014 Cutaneous Mastocytosis 53 0.065
327
BLN003 Blindness 53 0.065
328
RTC005 Reticulosarcoma 44 0.065
329
FLL019 Follicular Mucinosis 40 0.065
330
P RFR008 Refractory Anemia with Excess Blasts 34 0.065
331
FSR001 Fusariosis 28 0.065
332
MN1001 Mn1 21 0.065
333
P FRD001 Friedreich Ataxia 67 0.064
334
c UVT001 Uveitis 66 0.064
335
P FTL006 Fetal Alcohol Spectrum Disorder 60 0.064
336
RHB003 Rhabdomyosarcoma 59 0.064
337
P CRV039 Cervicitis 58 0.064
338
LKP004 Leukopenia 45 0.064
339
P SDR003 Sideroblastic Anemia 44 0.064
340
P SYS001 Systemic Lupus Erythematosus 88 0.062
341
P GST019 Gastrointestinal Stromal Tumor 83 0.062
342
c LPS004 Lupus Erythematosus 77 0.062
343
P RBN001 Rubinstein-Taybi Syndrome 76 0.062
344
P PRP003 Porphyria Cutanea Tarda 75 0.062
345
GLN003 Glanzmann's Thrombasthenia 74 0.062
346
P RNL014 Renal Cell Carcinoma 64 0.062
347
CLT003 Colitis 64 0.062
348
HYP066 Hyperglycemia 62 0.062
349
PMP001 Pemphigus 60 0.062
350
HYP063 Hypersplenism 59 0.062
351
PRC012 Pericardial Effusion 58 0.062
352
P GLB002 Glioblastoma 58 0.062
353
P JVN003 Juvenile Xanthogranuloma 53 0.062
354
P PRP023 Peripheral Neuropathy 52 0.062
355
PLS025 Plasmablastic Lymphoma 52 0.062
356
OST019 Osteosclerosis 52 0.062
357
HYP025 Hyperphosphatemia 43 0.062
358
GRF001 Graft-Versus-Host Disease, Protection Against 32 0.062
359
c TTR021 Tetrasomy 21 30 0.062
360
P FML018 Familial Mediterranean Fever 76 0.060
361
c DBT009 Diabetes Mellitus 74 0.060
362
P RSP003 Respiratory Failure 70 0.060
363
c AMY001 Amyotrophic Lateral Sclerosis 67 0.060
364
c KBK001 Kabuki Syndrome 57 0.060
365
P PND001 Pain Disorder 52 0.060
366
P CHR092 Chronic Myeloproliferative Disease 50 0.060
367
PYM001 Pyomyositis 48 0.060
368
c HPT073 Hepatitis C Virus 48 0.060
369
P FLL037 Follicular Lymphoma 48 0.060
370
PRM041 Primary Cortisol Resistance 21 0.060
371
INF030 Infectious Mononucleosis 84 0.058
372
CRH001 Crohn's Disease 76 0.058
373
c PRM002 Primary Hyperoxaluria 74 0.058
374
P AST007 Astrocytoma 74 0.058
375
GLL008 Gilles De La Tourette Syndrome 71 0.058
376
P AMY004 Amyloidosis 68 0.058
377
P CLN016 Colon Cancer 65 0.058
378
SCB001 Scabies 61 0.058
379
IDP064 Idiopathic Neutropenia 61 0.058
380
PLS011 Plasmacytoma 57 0.058
381
P CTN015 Cutaneous T Cell Lymphoma 51 0.058
382
GRM009 Germ Cell Tumors 50 0.058
383
HYP017 Hypophosphatemia 49 0.058
384
LCT001 Lactic Acidosis 48 0.058
385
URT008 Urticaria Pigmentosa 47 0.058
386
DND018 Dendritic Cell Tumor 47 0.058
387
CYT008 Cytomegalovirus Infection 44 0.058
388
VRL011 Viral Infectious Disease 39 0.058
389
ATM004 Autoimmune Thrombocytopenic Purpura 68 0.056
390
c ENC004 Encephalitis 66 0.056
391
P PTT014 Pitt-Hopkins Syndrome 59 0.056
392
CLL003 Cellulitis 59 0.056
393
PRT011 Protein C Deficiency 56 0.056
394
KLN001 Klinefelter's Syndrome 56 0.056
395
PSD002 Pseudotumor Cerebri 55 0.056
396
INT221 Intravascular Large B-Cell Lymphoma 53 0.056
397
EWN002 Ewing's Family of Tumors 51 0.056
398
SFT003 Soft Tissue Sarcoma 49 0.056
399
LYM051 Lymphomatoid Granulomatosis 49 0.056
400
BCK006 Back Pain 39 0.056
401
3Q2002 3q21q26 Syndrome 28 0.056
402
ECT004 Ecthyma 28 0.056
403
P MYC007 Myocardial Infarction 93 0.054
404
ADN001 Adenosine Deaminase Deficiency 70 0.054
405
P THY023 Thymoma 68 0.054
406
P HYP117 Hypertriglyceridemia 67 0.054
407
BRN028 Brain Cancer 65 0.054
408
c ACT027 Acute Pancreatitis 64 0.054
409
FLT001 Felty's Syndrome 64 0.054
410
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.054
411
P SNS014 Sinusitis 58 0.054
412
P END033 Endocarditis 57 0.054
413
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.054
414
THY009 Thyroid Lymphoma 54 0.054
415
AGG002 Aggressive Systemic Mastocytosis 52 0.054
416
MNN014 Mononeuritis 51 0.054
417
P NRV007 Nervous System Disease 50 0.054
418
HYP005 Hypokalemia 50 0.054
419
EVN001 Evans' Syndrome 46 0.054
420
5QS001 5q- Syndrome 45 0.054
421
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.054
422
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 37 0.054
423
c LYM034 Lymphoproliferative Disease, X-Linked 29 0.054
424
c HRD009 Hereditary Wilms' Tumor 23 0.054
425
P RTT002 Rett Syndrome 83 0.052
426
P OST018 Osteosarcoma 82 0.052
427
P PLL001 Pallister-Hall Syndrome 71 0.052
428
P RTH001 Rothmund-Thomson Syndrome 70 0.052
429
MSL001 Measles 68 0.052
430
P NNN008 Noonan Syndrome 1 68 0.052
431
P OLG002 Oligodendroglioma 64 0.052
432
HPT022 Hepatoblastoma 62 0.052
433
BRN002 Bronchiolitis 61 0.052
434
MLL005 Miller-Dieker Syndrome 60 0.052
435
PRP007 Priapism 60 0.052
436
BRN012 Bronchiolitis Obliterans 60 0.052
437
PLY041 Polymyositis 59 0.052
438
PRT039 Proteinuria 58 0.052
439
TNS005 Tonsillitis 57 0.052
440
ACT100 Acute Febrile Neutrophilic Dermatosis 57 0.052
441
CYT005 Cytomegalovirus Retinitis 57 0.052
442
P EXN002 Exanthem 56 0.052
443
APP008 Appendicitis 56 0.052
444
P INF032 Infertility 55 0.052
445
PRM163 Primary Mediastinal Large B-Cell Lymphoma 53 0.052
446
GRN007 Granuloma Annulare 53 0.052
447
CLN015 Colon Adenocarcinoma 52 0.052
448
PRN049 Paraneoplastic Pemphigus 50 0.052
449
PRP036 Peripheral T-Cell Lymphoma 49 0.052
450
P MLG081 Malignant Teratoma 48 0.052
451
P HML001 Hemolytic-Uremic Syndrome 48 0.052
452
MMB001 Membranoproliferative Glomerulonephritis 48 0.052
453
PNN001 Panniculitis 47 0.052
454
DNR001 Duane Retraction Syndrome 45 0.052
455
ANP009 Anaplastic Oligodendroglioma 43 0.052
456
P DNS004 Duane Syndrome Type 2 39 0.052
457
SPL006 Splenic Infarction 39 0.052
458
TRS012 Trisomy 22 30 0.052
459
ACT176 Acute Panmyelosis with Myelofibrosis 22 0.052
460
OTP003 Oto-Palatal-Digital Syndrome 17 0.052
461
P CLR023 Colorectal Cancer 77 0.050
462
P LPR002 Leopard Syndrome 75 0.050
463
c CWD001 Cowden Disease 72 0.050
464
c THL005 Thalassemia 72 0.050
465
P MYS005 Myositis 70 0.050
466
c NPH012 Nephrotic Syndrome 67 0.050
467
PYR013 Pyruvate Kinase Deficiency 67 0.050
468
P LPS002 Liposarcoma 60 0.050
469
VNS009 Venous Thrombosis 60 0.050
470
P AVS004 Avascular Necrosis of the Femoral Head 59 0.050
471
c TRT010 Teratoma 59 0.050
472
CRY004 Cryoglobulinemia 59 0.050
473
MRK001 Merkel Cell Carcinoma 56 0.050
474
PLY020 Polyradiculoneuropathy 55 0.050
475
CRD001 Cardiac Tamponade 55 0.050
476
PRN011 Pernicious Anemia 53 0.050
477
c CPL003 Capillary Leak Syndrome 53 0.050
478
TLN003 Telangiectasis 49 0.050
479
GLM011 Glomerulosclerosis 48 0.050
480
LYM045 Lymphocytic Vasculitis 45 0.050
481
SPN060 Spondylocarpotarsal Synostosis Syndrome 43 0.050
482
FCT013 Factor V Leiden Thrombophilia 34 0.050
483
c TCL008 T-Cell Lymphoma 1a 12 0.050
484
P ALZ001 Alzheimer's Disease 100 0.047
485
KPS001 Kaposi's Sarcoma 87 0.047
486
P HMC003 Hemochromatosis 83 0.047
487
BLM001 Bloom Syndrome 74 0.047
488
SHW002 Shwachman-Diamond Syndrome 69 0.047
489
THR079 Thromboembolism 66 0.047
490
MLT022 Malt Lymphoma 63 0.047
491
c AGM001 Agammaglobulinemia 61 0.047
492
SPT013 Septic Shock 61 0.047
493
DNG003 Dengue Disease 60 0.047
494
P MMP001 Mumps 60 0.047
495
NRC020 Neuroectodermal Tumor 59 0.047
496
MYX005 Myxoid Liposarcoma 59 0.047
497
EXT010 Extramedullary Plasmacytoma 59 0.047
498
OST017 Osteomyelitis 59 0.047
499
NRH001 Neurohypophyseal Diabetes Insipidus 57 0.047
500
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 56 0.047
501
DND002 Dendritic Cell Sarcoma 56 0.047
502
PYD001 Pyoderma Gangrenosum 56 0.047
503
NTR001 Neutral Lipid Storage Disease 55 0.047
504
PST062 Pustulosis Palmaris Et Plantaris 54 0.047
505
c ACT134 Acute Liver Failure 54 0.047
506
PYD002 Pyoderma 51 0.047
507
LYM027 Lymphopenia 51 0.047
508
PRT026 Parotitis 50 0.047
509
c MSB002 Mesoblastic Nephroma 50 0.047
510
P CNG029 Congenital Mesoblastic Nephroma 48 0.047
511
GYN001 Gynecomastia 46 0.047
512
EPG003 Epiglottitis 41 0.047
513
ANG046 Angioimmunoblastic T-Cell Lymphoma 40 0.047
514
NRG004 Neurogenic Diabetes Insipidus 40 0.047
515
SPR035 Superior Vena Cava Syndrome 40 0.047
516
GST053 Gastric Cancer 38 0.047
517
c SRC025 Sarcoidosis 1 36 0.047
518
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 32 0.047
519
CYT004 Cytomegalic Inclusion Disease 30 0.047
520
ACQ031 Acquired Idiopathic Sideroblastic Anemia 29 0.047
521
IRN002 Iron Metabolism Disease 28 0.047
522
HPT070 Hepatosplenic T-Cell Lymphoma 26 0.047
523
CD4007 Cd4+/cd56+ Hematodermic Neoplasm 25 0.047
524
c RNG017 Ring Chromosome 21 24 0.047
525
P MDL005 Medulloblastoma 80 0.045
526
P PRM021 Primary Pulmonary Hypertension 77 0.045
527
THY028 Thyroid Cancer 75 0.045
528
P CHR071 Charcot-Marie-Tooth Disease 72 0.045
529
ACQ007 Acquired Immunodeficiency Syndrome 71 0.045
530
P FCL005 Focal Segmental Glomerulosclerosis 70 0.045
531
P KDN017 Kidney Cancer 70 0.045
532
P HYP056 Hypoglycemia 67 0.045
533
STR008 Strongyloidiasis 66 0.045
534
ANT006 Antiphospholipid Syndrome 66 0.045
535
c JVN010 Juvenile Rheumatoid Arthritis 66 0.045
536
c HMP007 Hemophilia 65 0.045
537
P LRY019 Laryngitis 65 0.045
538
P MYP004 Myopathy 62 0.045
539
CHL067 Cholecystitis 61 0.045
540
P END047 Endophthalmitis 60 0.045
541
PPL002 Papillary Carcinoma 59 0.045
542
CLD007 Cold Agglutinin Disease 59 0.045
543
RTN017 Retinal Detachment 56 0.045
544
P THR012 Thoracic Cancer 55 0.045
545
PRC013 Pericarditis 53 0.045
546
GRW007 Growth Hormone Deficiency 52 0.045
547
NRF008 Neurofibromatosis-Noonan Syndrome 52 0.045
548
OBS001 Obstructive Jaundice 51 0.045
549
RTN001 Retinal Vasculitis 51 0.045
550
P ALV004 Alveolar Rhabdomyosarcoma 50 0.045
551
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 48 0.045
552
LYM021 Lymphadenitis 48 0.045
553
LKP003 Leukoplakia 46 0.045
554
ANR040 Aneurysm 46 0.045
555
THR035 Thrombasthenia 45 0.045
556
MLG083 Male Germ Cell Tumor 45 0.045
557
TST015 Testicular Disease 42 0.045
558
ANG037 Angiomatosis 38 0.045
559
NRW001 Norwegian Scabies 35 0.045
560
PNM003 Pneumatosis Cystoides Intestinalis 25 0.045
561
RFR007 Refractory Anemia with Excess Blasts in Transformation 20 0.045
562
GLC006 Galactosemia 86 0.042
563
c BTT002 Beta Thalassemia 78 0.042
564
P MYS003 Myasthenia Gravis 78 0.042
565
SKN016 Skin Disease 75 0.042
566
c PLM037 Pulmonary Hypertension 73 0.042
567
P TMP003 Temporal Arteritis 72 0.042
568
P MLG075 Malignant Mesothelioma 69 0.042
569
P BCK002 Beckwith-Wiedemann Syndrome 68 0.042
570
ACT049 Acute Disseminated Encephalomyelitis 67 0.042
571
P ATM006 Autoimmune Lymphoproliferative Syndrome 67 0.042
572
c JBR001 Joubert Syndrome 66 0.042
573
ADN018 Adenoma 66 0.042
574
ULC004 Ulcerative Colitis 65 0.042
575
P INS005 Insulin Resistance 65 0.042
576
c HYP076 Hyperthyroidism 64 0.042
577
P FBR017 Fibrosarcoma 63 0.042
578
SCK005 Sickle Cell Disease 62 0.042
579
P LMY004 Leiomyosarcoma 62 0.042
580
c ALM001 Al Amyloidosis 61 0.042
581
GLL022 Guillain-Barre Syndrome 61 0.042
582
PST046 Post-Transplant Lymphoproliferative Disease 60 0.042
583
CHC001 Chickenpox 60 0.042
584
c ACT075 Acute Myocardial Infarction 60 0.042
585
P PRM011 Primary Ciliary Dyskinesia 59 0.042
586
MRG003 Marginal Zone B-Cell Lymphoma 59 0.042
587
c HRD010 Hereditary Spastic Paraplegia 58 0.042
588
FLL008 Folliculitis 58 0.042
589
ORL005 Oral Candidiasis 58 0.042
590
PLM020 Pleomorphic Xanthoastrocytoma 58 0.042
591
c CNT016 Central Retinal Vein Occlusion 58 0.042
592
LRY018 Laryngeal Squamous Cell Carcinoma 57 0.042
593
c HRD001 Hereditary Multiple Exostoses 57 0.042
594
c PST005 Posterior Uveitis 57 0.042
595
BLS002 Blastomycosis 57 0.042
596
P JBR004 Joubert Syndrome 2 56 0.042
597
NCR004 Nocardiosis 56 0.042
598
CRD005 Cardia Cancer 56 0.042
599
GST050 Gastrointestinal System Disease 56 0.042
600
P FNC025 Fanconi Anemia, Complementation Group J 55 0.042
601
CHR008 Choroiditis 54 0.042
602
SPT004 Septic Arthritis 53 0.042
603
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 53 0.042
604
STN007 Stenotrophomonas Maltophilia 53 0.042
605
RSC001 Rosacea 52 0.042
606
c ACQ014 Acquired Hemophilia 52 0.042
607
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 50 0.042
608
THY022 Thymic Carcinoma 49 0.042
609
GNG002 Ganglioneuroma 49 0.042
610
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.042
611
c DMY001 Demyelinating Polyneuropathy 47 0.042
612
RPP001 Rapp-Hodgkin Syndrome 47 0.042
613
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 46 0.042
614
GLM037 Glioma Somatic 46 0.042
615
ILS001 Ileus 45 0.042
616
TCL003 T Cell Deficiency 45 0.042
617
SPR033 Superficial Spreading Melanoma 43 0.042
618
c HRD086 Hereditary Hypophosphatemic Rickets 42 0.042
619
P LSS005 Lissencephaly 1 40 0.042
620
CMP001 Composite Lymphoma 39 0.042
621
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 39 0.042
622
HMR023 Hemorrhagic Cystitis 38 0.042
623
PRL008 Paralytic Ileus 36 0.042
624
IMM088 Immunodeficiency 36 34 0.042
625
BLT011 Bilateral Perisylvian Polymicrogyria 34 0.042
626
CHR020 Chronic Interstitial Cystitis 34 0.042
627
CLC008 Colchicine Resistance 32 0.042
628
MTR008 Mature B-Cell Neoplasm 31 0.042
629
SPL007 Splenic Abscess 31 0.042
630
c DYS055 Dystonia 10 27 0.042
631
HYP179 Hypertrichosis Congenital Generalized X-Linked 26 0.042
632
RHB020 Rhabdomyosarcoma, Somatic 26 0.042
633
EXF003 Exfoliative Dermatitis 25 0.042
634
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 21 0.042
635
P GCH001 Gaucher's Disease 84 0.040
636
ESP021 Esophageal Cancer 80 0.040
637
HST011 Histoplasmosis 73 0.040
638
P DRM010 Dermatomyositis 71 0.040
639
P STM004 Stomach Cancer 69 0.040
640
HPT002 Hepatic Vein Thrombosis 66 0.040
641
PRP025 Peripheral Primitive Neuroectodermal Tumor 65 0.040
642
P ADL010 Adult Respiratory Distress Syndrome 64 0.040
643
P ART023 Arthropathy 64 0.040
644
CMP002 Campylobacteriosis 63 0.040
645
PSR002 Psoriasis 63 0.040
646
GRY002 Gray Platelet Syndrome 63 0.040
647
c MSC005 Muscular Dystrophy 62 0.040
648
P CRD013 Cardiofaciocutaneous Syndrome 62 0.040
649
P CNJ013 Conjunctivitis 62 0.040
650
SRS001 Serous Cystadenocarcinoma 61 0.040
651
P SCL015 Scleritis 61 0.040
652
MLR002 Miliary Tuberculosis 60 0.040
653
c THR005 Thrombotic Thrombocytopenic Purpura 59 0.040
654
c MTH007 Methemoglobinemia 59 0.040
655
ANT009 Antithrombin Iii Deficiency 59 0.040
656
PRN001 Purine Nucleoside Phosphorylase Deficiency 59 0.040
657
END030 End Stage Renal Failure 58 0.040
658
LST001 Listeriosis 58 0.040
659
BRN029 Brain Disease 58 0.040
660
P SDR002 Siderosis 58 0.040
661
GLB015 Glioblastoma Multiforme 58 0.040
662
P RTN022 Retinal Vein Occlusion 57 0.040
663
P RPD001 Rapidly Progressive Glomerulonephritis 57 0.040
664
ALP008 Alopecia 57 0.040
665
EPD001 Epidermodysplasia Verruciformis 57 0.040
666
P CMP008 Compartment Syndrome 56 0.040
667
DDN006 Duodenitis 56 0.040
668
TLP001 Talipes Equinovarus 56 0.040
669
RDC002 Radiculopathy 56 0.040
670
FBR003 Fibrous Histiocytoma 55 0.040
671
HST009 Histiocytoma 55 0.040
672
NPH051 Nephritis 54 0.040
673
ORL011 Oral Cancer 54 0.040
674
PTS001 Patau Syndrome 53 0.040
675
CLC006 Calcinosis 53 0.040
676
HYP037 Hyperhomocysteinemia 53 0.040
677
TRP014 Triploidy 52 0.040
678
HPT032 Hepatocellular Carcinoma, Somatic 52 0.040
679
MNT147 Mental Retardation 52 0.040
680
ORC001 Orchitis 51 0.040
681
MLK003 Melkersson-Rosenthal Syndrome 51 0.040
682
P WLD002 Waldenstrom Macroglobulinemia 51 0.040
683
HYP068 Hyperostosis 50 0.040
684
MCR020 Microsporidiosis 50 0.040
685
OLG006 Oligoastrocytoma 49 0.040
686
c PRM046 Primary Malignant Lymphoma 49 0.040
687
PLR008 Pleurisy 48 0.040
688
PRP016 Paraplegia 48 0.040
689
PRN039 Paraneoplastic Syndromes 47 0.040
690
LYM012 Lymphoplasmacytic Lymphoma 46 0.040
691
PRM097 Primary Immunodeficiency Disease 46 0.040
692
ECT026 Ectopic Pregnancy 46 0.040
693
UTR043 Uterine Sarcoma 45 0.040
694
HDR003 Hidradenitis 44 0.040
695
OLG015 Oligoarticular Juvenile Arthritis 43 0.040
696
MYC017 Mycobacterium Kansasii 42 0.040
697
CDQ001 Cauda Equina Syndrome 42 0.040
698
ACL001 Acalculous Cholecystitis 41 0.040
699
HTL002 Htlv-1 Associated Myelopathy 39 0.040
700
c HYD008 Hydrocephalus Due to Aqueductal Stenosis 36 0.040
701
CYC007 Cyclic Thrombocytopenia 36 0.040
702
INT038 Interdigitating Dendritic Cell Sarcoma 36 0.040
703
BRT011 Bruton-Type Agammaglobulinemia 36 0.040
704
PLY010 Polyclonal Hypergammaglobulinemia 36 0.040
705
MYL013 Myeloperoxidase Deficiency 34 0.040
706
HPT012 Hepatocellular Fibrolamellar Carcinoma 33 0.040
707
NTR005 Nutritional Deficiency Disease 33 0.040
708
MLG041 Malignant Triton Tumor 31 0.040
709
ANP008 Anaplastic Oligoastrocytoma 28 0.040
710
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 22 0.040
711
BLD053 Blood Platelet Disease 21 0.040
712
SML025 Small Non-Cleaved Cell Lymphoma 21 0.040
713
GNR023 Generalized Eruptive Histiocytosis 21 0.040
714
MYL004 Myelodysplastic Myeloproliferative Cancer 21 0.040
715
c CHR257 Chromosome 6q Deletion 20 0.040
716
CYT018 Cytochrome P450 2d6 Variant 16 0.040
717
ALD004 Ala Dehydratase Deficiency 12 0.040
718
INC002 Inclusion Body Myositis 86 0.037
719
P OVR042 Ovarian Cancer 85 0.037
720
SCK003 Sickle Cell Anemia 82 0.037
721
ACR007 Acromegaly 80 0.037
722
KWS002 Kawasaki Disease 76 0.037
723
P MLR004 Malaria 75 0.037
724
LSH001 Leishmaniasis 74 0.037
725
P HRD008 Hereditary Hemorrhagic Telangiectasia 73 0.037
726
CHR012 Chronic Granulomatous Disease 71 0.037
727
P MTB001 Metabolic Syndrome X 70 0.037
728
LKC001 Leukocyte Adhesion Deficiency 69 0.037
729
P MLG068 Malignant Glioma 69 0.037
730
P LVR013 Liver Disease 69 0.037
731
THR016 Thrombophlebitis 69 0.037
732
NNS005 Non-Small Cell Lung Carcinoma 69 0.037
733
P BLD042 Bladder Carcinoma 68 0.037
734
GSG001 Gas Gangrene 68 0.037
735
CMM004 Common Variable Immunodeficiency 67 0.037
736
P THR015 Thrombophilia 67 0.037
737
P PRT013 Portal Hypertension 66 0.037
738
P ALP009 Alopecia Areata 65 0.037
739
CRY003 Cryptosporidiosis 64 0.037
740
P RBL001 Rubella 63 0.037
741
CLN045 Colonic Benign Neoplasm 63 0.037
742
P ATY010 Atypical Hemolytic-Uremic Syndrome 62 0.037
743
TYP007 Typhoid Fever 62 0.037
744
VGT001 Vogt-Koyanagi-Harada Disease 61 0.037
745
XLN001 X-Linked Ichthyosis 61 0.037
746
c ATM011 Autoimmune Hepatitis 61 0.037
747
P CRT033 Corticobasal Degeneration 59 0.037
748
AMN001 Amenorrhea 59 0.037
749
KNN001 Kennedy's Disease 59 0.037
750
CLS007 Classic Kaposi Sarcoma 58 0.037
751
P MYC008 Myocarditis 58 0.037
752
INT054 Intraocular Lymphoma 58 0.037
753
SPN051 Spondylitis 58 0.037
754
P PLC011 Pilocytic Astrocytoma 57 0.037
755
c XRD019 Xeroderma Pigmentosum, Group C 56 0.037
756
ILT001 Ileitis 56 0.037
757
P HYP014 Hyperuricemia 56 0.037
758
VNS010 Venous Thromboembolism 55 0.037
759
P DWR001 Dwarfism 55 0.037
760
P SML034 Small Cell Neuroendocrine Carcinoma 55 0.037
761
c XRD012 Xeroderma Pigmentosum, Group D 55 0.037
762
PTT004 Pituitary Apoplexy 54 0.037
763
PPL021 Papilledema 54 0.037
764
P INT072 Intestinal Pseudo-Obstruction 54 0.037
765
ACT008 Actinic Keratosis 54 0.037
766
c LTR001 Lateral Sclerosis 54 0.037
767
c OPH004 Ophthalmoplegia 53 0.037
768
PNM001 Pneumocystosis 53 0.037
769
INT075 Intracranial Hypertension 53 0.037
770
HNT002 Hantavirus Pulmonary Syndrome 53 0.037
771
c LYM025 Lymphedema 53 0.037
772
RSD004 Rosai-Dorfman Disease 53 0.037
773
c CNG027 Congenital Hemolytic Anemia 52 0.037
774
FRZ001 Frozen Shoulder 52 0.037
775
GNG005 Gangliocytoma 52 0.037
776
P GRV001 Graves' Disease 51 0.037
777
GST027 Gastric Lymphoma 51 0.037
778
OVR012 Ovarian Serous Cystadenocarcinoma 51 0.037
779
SGT001 Sagittal Sinus Thrombosis 50 0.037
780
LMB024 Limbic Encephalitis 49 0.037
781
TXC002 Toxic Encephalopathy 49 0.037
782
P PRM012 Primary Polycythemia 49 0.037
783
PDT021 Pediatric Osteosarcoma 49 0.037
784
GNT031 Genitopatellar Syndrome 49 0.037
785
PRN029 Parainfluenza Virus Type 3 49 0.037
786
PNV001 Panuveitis 48 0.037
787
CRY001 Cryptogenic Organizing Pneumonia 48 0.037
788
CHY006 Chylous Ascites 48 0.037
789
PRT038 Protein-Energy Malnutrition 48 0.037
790
PRG060 Pregnancy Loss 48 0.037
791
END021 Endomyocardial Fibrosis 47 0.037
792
SPL004 Splenic Marginal Zone Lymphoma 47 0.037
793
MNN009 Meningoencephalitis 47 0.037
794
MCP006 Mucoepidermoid Carcinoma 46 0.037
795
PNH001 Panhypopituitarism 46 0.037
796
FSC004 Fasciitis 46 0.037
797
MCR017 Macrocytic Anemia 45 0.037
798
MLN057 Melanoma of Soft Parts 45 0.037
799
c APH002 Aphasia 44 0.037
800
c CNG003 Congenital Dyserythropoietic Anemia 43 0.037
801
LYM105 Lymphoma, Follicular, Somatic 39 0.037
802
MNN002 Mononeuritis Multiplex 38 0.037
803
PHH001 Phaeohyphomycosis 38 0.037
804
MSN004 Mesenchymal Cell Neoplasm 38 0.037
805
P SYS007 Systemic Capillary Leak Syndrome 37 0.037
806
PLY021 Polyradiculopathy 33 0.037
807
P HRD104 Hereditary Multiple Osteochondromas 33 0.037
808
XLN009 X-Linked Spinal-Bulbar Muscle Atrophy 33 0.037
809
THY025 Thymus Cancer 33 0.037
810
P CRN035 Cranial Nerve Palsy 32 0.037
811
LNG004 Langerhans Cell Sarcoma 30 0.037
812
DNG004 Dengue Fever, Protection Against 29 0.037
813
THP001 Thiopurine S Methyltranferase Deficiency 28 0.037
814
IMM001 Immune-Complex Glomerulonephritis 27 0.037
815
TRN028 Transient Acantholytic Dermatosis 26 0.037
816
DSC004 Discitis 26 0.037
817
ORB012 Orbital Cancer 24 0.037
818
MYL049 Myelofibrosis, Somatic 23 0.037
819
VRS001 Virus Associated Hemophagocytic Syndrome 21 0.037
820
DMD001 Demodicidosis 20 0.037
821
HRD137 Hereditary Isolated Aplastic Anemia 19 0.037
822
MLT034 Multicystic Renal Dysplasia, Bilateral 18 0.037
823
RDT006 Radiation Induced Meningioma 18 0.037
824
PRK066 Parkinsonism with Spasticity, X-Linked 18 0.037
825
P TYP008 Type 1 Diabetes Mellitus 96 0.034
826
PHN003 Phenylketonuria 83 0.034
827
P WSK001 Wiskott-Aldrich Syndrome 79 0.034
828
FCT007 Factor Vii Deficiency 79 0.034
829
CLD001 Cleidocranial Dysplasia 79 0.034
830
CHD001 Chediak-Higashi Syndrome 76 0.034
831
P OST002 Osteoporosis 76 0.034
832
P ALP006 Alpha Thalassemia 75 0.034
833
PRT036 Peritonitis 72 0.034
834
DBT011 Diabetic Retinopathy 71 0.034
835
P CNG401 Congenital Heart Disease 69 0.034
836
P RCK004 Rickets 68 0.034
837
CHR003 Cherubism 68 0.034
838
MLB002 Male Breast Cancer 68 0.034
839
PRP027 Peripheral Vascular Disease 68 0.034
840
PLS006 Plasmodium Vivax Malaria 68 0.034
841
GST023 Gastric Ulcer 67 0.034
842
ALP001 Alopecia Universalis 67 0.034
843
P HRD057 Hereditary Pancreatitis 66 0.034
844
P OST001 Osteopetrosis 66 0.034
845
P BRN019 Bernard-Soulier Syndrome 65 0.034
846
c MCP010 Mucopolysaccharidosis 64 0.034
847
PMS001 Poems Syndrome 64 0.034
848
P ESP024 Esophagitis 64 0.034
849
c INT070 Intestinal Obstruction 63 0.034
850
c THN001 Thanatophoric Dysplasia 62 0.034
851
P KRT004 Keratitis 62 0.034
852
RBR001 Roberts Syndrome 62 0.034
853
LBR002 Leber Hereditary Optic Neuropathy 62 0.034
854
TST014 Testicular Cancer 62 0.034
855
P CRV035 Cervical Cancer 61 0.034
856
CHR074 Choriocarcinoma 61 0.034
857
ASP003 Aseptic Meningitis 61 0.034
858
GLS001 Gliosarcoma 61 0.034
859
VSC003 Visceral Leishmaniasis 61 0.034
860
SPN020 Spondylosis 60 0.034
861
P PRM054 Primary Sclerosing Cholangitis 60 0.034
862
c GLY013 Glycogen Storage Disease 60 0.034
863
MLT001 Multiple Chemical Sensitivity 60 0.034
864
CNG402 Congenital Insensitivity to Pain with Anhidrosis 59 0.034
865
INT051 Intussusception 59 0.034
866
ANR004 Anuria 59 0.034
867
TBR011 Tuberculous Meningitis 59 0.034
868
DBL002 Double Outlet Right Ventricle 58 0.034
869
SCN006 Secondary Syphilis 57 0.034
870
EXF001 Exfoliation Syndrome 57 0.034
871
TTH006 Tooth Disease 56 0.034
872
STV001 Stevens-Johnson Syndrome 56 0.034
873
INS008 Insulin-Like Growth Factor I Deficiency 56 0.034
874
ACR005 Acrodermatitis 55 0.034
875
LMB002 Lambert-Eaton Myasthenic Syndrome 55 0.034
876
MLN020 Melanoma, Malignant, Somatic 55 0.034
877
P CHR019 Choroid Plexus Carcinoma 55 0.034
878
MYL001 Myelitis 55 0.034
879
PRT018 Portal Vein Thrombosis 55 0.034
880
c LPR012 Leopard Syndrome 1 54 0.034
881
c ANT034 Anterior Uveitis 54 0.034
882
CYC004 Cyclic Hematopoiesis 54 0.034
883
c DFF019 Diffuse Gastric Cancer 54 0.034
884
PLM012 Pulmonary Sarcoidosis 53 0.034
885
P PRN022 Perineurioma 53 0.034
886
NM001 Noma 53 0.034
887
EMP001 Empty Sella Syndrome 52 0.034
888
GNG012 Gingival Overgrowth 52 0.034
889
c DRR001 Diarrhea 52 0.034
890
P CYS018 Cystitis 51 0.034
891
ERY003 Erythema Multiforme 51 0.034
892
P BRY001 Berylliosis 51 0.034
893
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 51 0.034
894
APP001 Apparent Mineralocorticoid Excess Syndrome 51 0.034
895
STM007 Stomatitis 51 0.034
896
ASB001 Asbestosis 51 0.034
897
c ERY013 Erythrocytosis 50 0.034
898
SPN032 Spindle Cell Carcinoma 50 0.034
899
GST014 Gastrointestinal Lymphoma 50 0.034
900
CWP001 Cowpox 50 0.034
901
CRB090 Cerebral Hypoxia 49 0.034
902
MLG121 Male Germ Cell Tumor, Somatic 49 0.034
903
NPH003 Nephrocalcinosis 49 0.034
904
BLT006 Bilateral Breast Cancer 48 0.034
905
LYM052 Lymphomatoid Papulosis 47 0.034
906
GNG008 Ganglioneuroblastoma 47 0.034
907
DRM011 Dermatophytosis 47 0.034
908
CNT025 Central Pontine Myelinolysis 47 0.034
909
P PLG001 Pelger-Huet Anomaly 47 0.034
910
ACT167 Acute Generalized Exanthematous Pustulosis 46 0.034
911
DFF024 Diffuse Panbronchiolitis 46 0.034
912
BLD101 Bladder Cancer Susceptibility 45 0.034
913
FST010 Fasting Hypoglycemia 44 0.034
914
BRS069 Breast Cancer, Somatic 44 0.034
915
FML055 Familial Cylindromatosis 44 0.034
916
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.034
917
NCR007 Necrotizing Fasciitis 44 0.034
918
SNL007 Senile Cataract 43 0.034
919
GND001 Gonadoblastoma 43 0.034
920
NPH017 Nephrosis 42 0.034
921
P DCR003 Dacryoadenitis 42 0.034
922
5FL001 5-Fluorouracil Toxicity 42 0.034
923
FBR002 Fibrosarcoma of Bone 42 0.034
924
c CHR208 Chromosome 17p Deletion 41 0.034
925
PRM014 Periampullary Adenocarcinoma 41 0.034
926
c CHR253 Chromosome 5q Deletion 40 0.034
927
CRB085 Cerebral Hemorrhage 39 0.034
928
P OTT001 Otitis Externa 39 0.034
929
SBC024 Subcutaneous Panniculitis-Like T-Cell Lymphoma 38 0.034
930
BNZ002 Benzene Toxicity 38 0.034
931
ERY045 Erythrocytosis, Somatic 38 0.034
932
ANM001 Anemia of Prematurity 37 0.034
933
TLS001 Tolosa-Hunt Syndrome 37 0.034
934
DST056 Distal 22q11.2 Microdeletion Syndrome 37 0.034
935
GRN009 Granulomatous Hepatitis 36 0.034
936
BRC011 Brachial Plexus Neuropathy 35 0.034
937
PLM074 Pulmonary Function 34 0.034
938
ABL001 Ablepharon Macrostomia Syndrome 34 0.034
939
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 33 0.034
940
EPD018 Epididymo-Orchitis 32 0.034
941
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 32 0.034
942
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.034
943
c CNG023 Congenital Fibrosarcoma 31 0.034
944
CRN061 Corneal Dystrophy Avellino Type 29 0.034
945
c ATX026 Ataxia-Telangiectasia Variant 28 0.034
946
PRR008 Periarteritis Nodosa 28 0.034
947
P FNC044 Fanconi Anemia, Complementation Group C 28 0.034
948
c ATS021 Autosomal Recessive Juvenile Parkinson Disease 27 0.034
949
BLN009 Balanoposthitis 25 0.034
950
PL2001 Pla2g6-Associated Neurodegeneration 25 0.034
951
PRD013 Periodic Fever, Familial, Autosomal Dominant 24 0.034
952
CRT009 Critical Illness Polyneuropathy 24 0.034
953
c MLG036 Malignant Spiradenoma 23 0.034
954
c RNG024 Ring Chromosome 8 23 0.034
955
P BKV001 Bk-Virus Nephropathy 23 0.034
956
CHR463 Chronic Actinic Dermatitis 23 0.034
957
IND005 Indolent B Cell Lymphoma 21 0.034
958
EXT039 Extrapontine Myelinolysis 21 0.034
959
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 21 0.034
960
CD3004 Cd3epsilon Deficiency 20 0.034
961
MRC006 Mercaptopurine Toxicity 8 0.034
962
c TYP009 Type 2 Diabetes Mellitus 100 0.030
963
CYS001 Cystic Fibrosis 97 0.030
964
P FML011 Familial Adenomatous Polyposis 89 0.030
965
P AST005 Asthma 89 0.030
966
CDS001 Cadasil 84 0.030
967
VNH001 Von Hippel-Lindau Disease 81 0.030
968
WLS001 Wilson Disease 79 0.030
969
ACH004 Achondroplasia 78 0.030
970
P LPR003 Leprosy 78 0.030
971
P ALX003 Alexander Disease 76 0.030
972
CYS013 Cystinuria 76 0.030
973
P CLC005 Celiac Disease 73 0.030
974
CCC001 Coccidioidomycosis 72 0.030
975
RLP001 Relapsing Polychondritis 72 0.030
976
WRN001 Werner Syndrome 72 0.030
977
GNT003 Genital Herpes 70 0.030
978
P MLT042 Multiple Endocrine Neoplasia Type 2a 70 0.030
979
BLL006 Bullous Pemphigoid 70 0.030
980
PLY017 Polyarteritis Nodosa 69 0.030
981
CRY005 Cryptococcosis 68 0.030
982
TRG002 Trigeminal Neuralgia 67 0.030
983
P TRN020 Turner Syndrome 67 0.030
984
PBL001 Piebaldism 66 0.030
985
P GST044 Gastritis 66 0.030
986
ALS001 Alstrom Syndrome 66 0.030
987
c TXP001 Toxoplasmosis 66 0.030
988
DBT001 Diabetic Ketoacidosis 66 0.030
989
P RHN004 Rhinitis 65 0.030
990
OMN001 Omenn Syndrome 65 0.030
991
DBN001 Dubin-Johnson Syndrome 65 0.030
992
c LNG028 Long Qt Syndrome 65 0.030
993
PRT014 Protein S Deficiency 65 0.030
994
STR067 Stroke, Ischemic 65 0.030
995
TTN003 Tetanus 65 0.030
996
BRR003 Barrett's Esophagus 64 0.030
997
MXD005 Mixed Connective Tissue Disease 64 0.030
998
P VLC001 Velocardiofacial Syndrome 64 0.030
999
P ERY008 Erythromelalgia 64 0.030
1000
ISC004 Ischemia 63 0.030
1001
LYM009 Lymphocytic Choriomeningitis 63 0.030
1002
CRN036 Craniopharyngioma 63 0.030
1003
PRL009 Prolactinoma 63 0.030
1004
KRN002 Kearns-Sayre Syndrome 63 0.030
1005
ALP007 Alpha 1-Antitrypsin Deficiency 62 0.030
1006
GLD001 Goldenhar Syndrome 62 0.030
1007
c LMB006 Limb-Girdle Muscular Dystrophy 61 0.030
1008
CDL003 Caudal Regression Syndrome 61 0.030
1009
c ANG015 Angioedema 61 0.030
1010
BRC012 Brucellosis 61 0.030
1011
P BRN009 Burning Mouth Syndrome 60 0.030
1012
P PRC019 Precocious Puberty 60 0.030
1013
c LRY016 Laryngeal Carcinoma 60 0.030
1014
P SYN007 Synovitis 60 0.030
1015
ACR008 Acrocallosal Syndrome 60 0.030
1016
MCS003 Mucous Membrane Pemphigoid 60 0.030
1017
SLD003 Sialadenitis 59 0.030
1018
c HPT003 Hepatitis a 59 0.030
1019
ACR003 Acrodermatitis Enteropathica 59 0.030
1020
LPD010 Lipodystrophy 59 0.030
1021
TMP001 Temporal Lobe Epilepsy 59 0.030
1022
c BRG001 Brugada Syndrome 59 0.030
1023
c CHR023 Charcot-Marie-Tooth Disease Type 2 59 0.030
1024
CNN005 Connective Tissue Disease 58 0.030
1025
HDC001 Headache 58 0.030
1026
FLR002 Filariasis 58 0.030
1027
ICH002 Ichthyosis Bullosa of Siemens 58 0.030
1028
c CNG124 Congenital Rubella 58 0.030
1029
ACN011 Acne 58 0.030
1030
P MYM002 Moyamoya Disease 58 0.030
1031
INT146 Intervertebral Disc Disease 58 0.030
1032
P GNT008 Giant Cell Tumor 58 0.030
1033
c CTR002 Cataract 57 0.030
1034
ETN001 Eating Disorder 57 0.030
1035
P HYP024 Hypoparathyroidism 57 0.030
1036
P WVR001 Weaver Syndrome 57 0.030
1037
NDL013 Nodular Regenerative Hyperplasia 57 0.030
1038
ACN001 Acinar Cell Carcinoma 55 0.030
1039
BRN004 Brain Edema 55 0.030
1040
NPH011 Nephroblastoma 55 0.030
1041
P INT064 Intermediate Uveitis 55 0.030
1042
DBT006 Diabetic Macular Edema 54 0.030
1043
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 54 0.030
1044
ANH002 Anhidrosis 54 0.030
1045
P HYP141 Hyperphenylalaninemia 54 0.030
1046
PTT037 Pituitary Tumors 54 0.030
1047
IGG001 Iga Glomerulonephritis 54 0.030
1048
c PST022 Posterior Uveal Melanoma 54 0.030
1049
TNG003 Tongue Cancer 54 0.030
1050
DSM007 Desmoplastic Small Round Cell Tumor 54 0.030
1051
P SJG002 Sjogren-Larsson Syndrome 54 0.030
1052
GST045 Gastroenteritis 54 0.030
1053
PLY013 Polymyalgia Rheumatica 53 0.030
1054
ATY008 Atypical Lipomatous Tumor 53 0.030
1055
LPS007 Lupus Nephritis 53 0.030
1056
PRP002 Periapical Granuloma 53 0.030
1057
MMB002 Membranous Glomerulonephritis 53 0.030
1058
c HPT007 Hepatitis E 53 0.030
1059
GLS007 Glossitis 52 0.030
1060
HMR002 Hemarthrosis 52 0.030
1061
JVN033 Juvenile Nasopharyngeal Angiofibroma 52 0.030
1062
c FML024 Familial Melanoma 52 0.030
1063
ADN014 Adenomatoid Tumor 52 0.030
1064
c TLN008 Telangiectasia, Hereditary Hemorrhagic, Type 5 51 0.030
1065
JNT002 Joint Disorders 51 0.030
1066
MLL001 Molluscum Contagiosum 51 0.030
1067
LPD004 Lipoid Nephrosis 51 0.030
1068
PRT019 Protein-Losing Enteropathy 51 0.030
1069
WBR001 Weber Syndrome 51 0.030
1070
c KRT005 Keratoacanthoma 51 0.030
1071
P CST002 Castleman's Disease 51 0.030
1072
RHB017 Rhabdoid Tumor 51 0.030
1073
FBR009 Fibrous Dysplasia 51 0.030
1074
MMR004 Memory Impairment 51 0.030
1075
BRN018 Borna Disease 51 0.030
1076
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 51 0.030
1077
FCT005 Factor Xiii Deficiency 50 0.030
1078
ANL011 Anal Canal Carcinoma 50 0.030
1079
c ATM024 Autoimmune Pancreatitis 50 0.030
1080
OPT009 Optic Neuritis 50 0.030
1081
INF058 Inflammatory Myofibroblastic Tumor 50 0.030
1082
PYG006 Pyogenic Granuloma 50 0.030
1083
P PRK001 Porokeratosis 50 0.030
1084
CHR288 Chronic Recurrent Multifocal Osteomyelitis 50 0.030
1085
NRT004 Neuritis 49 0.030
1086
SMN007 Seminoma 49 0.030
1087
MDT001 Mediterranean Spotted Fever 49 0.030
1088
RTN003 Retinal Ischemia 49 0.030
1089
CNV002 Conversion Disorder 49 0.030
1090
TRC040 Tracheoesophageal Fistula 49 0.030
1091
CRY021 Cryoglobulinemic Vasculitis 48 0.030
1092
ESN006 Eosinophilic Meningitis 48 0.030
1093
IMM030 Immunodeficiency, Common Variable, 3 48 0.030
1094
VTM002 Vitamin B12 Deficiency 48 0.030
1095
URT010 Ureteral Obstruction 47 0.030
1096
MTG002 Mutagen Sensitivity 47 0.030
1097
c ATM019 Autoimmune Polyendocrine Syndrome 47 0.030
1098
P ART084 Arteriovenous Fistula 47 0.030
1099
PLS009 Plasma Cell Neoplasm 47 0.030
1100
TNS001 Tenosynovial Giant Cell Tumor 47 0.030
1101
MCR037 Macroglossia 47 0.030
1102
c CHR048 Chronic Rhinitis 46 0.030
1103
c RCR022 Recurrent Acute Pancreatitis 46 0.030
1104
P BRS044 Breast Adenocarcinoma 46 0.030
1105
MXL004 Maxillary Sinus Squamous Cell Carcinoma 46 0.030
1106
STC004 Stachybotrys Chartarum 46 0.030
1107
DHY007 Dihydropteridine Reductase Deficiency 46 0.030
1108
EPL002 Epilepsy Syndrome 46 0.030
1109
PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 46 0.030
1110
GMM002 Gamma Chain Deficiency 46 0.030
1111
BWN003 Bowenoid Papulosis 46 0.030
1112
INT067 Interstitial Nephritis 45 0.030
1113
P NRL007 Neurologic Diseases 45 0.030
1114
ADR021 Adrenocorticotropic Hormone Deficiency 45 0.030
1115
INF034 Infective Endocarditis 45 0.030
1116
CHR404 Chronic Granulomatous Disease Due to Deficiency of Ncf-1 45 0.030
1117
SPR005 Superficial Basal Cell Carcinoma 45 0.030
1118
c TRC005 Tracheal Stenosis 45 0.030
1119
CRB088 Cerebral Atrophy 44 0.030
1120
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 44 0.030
1121
RPD002 Rapadilino Syndrome 44 0.030
1122
QDR001 Quadriplegia 44 0.030
1123
DYS101 Dysgerminoma 43 0.030
1124
CND006 Candida Glabrata 43 0.030
1125
PLR005 Pleuropneumonia 43 0.030
1126
MYC019 Mycobacterium Marinum 43 0.030
1127
THY043 Thymic Hyperplasia 43 0.030
1128
TRT001 Teratocarcinoma 43 0.030
1129
P IRD010 Iridogoniodysgenesis Syndrome 43 0.030
1130
EST005 Esotropia 43 0.030
1131
c BRS076 Breast Cancer, Early-Onset 43 0.030
1132
INT071 Intestinal Perforation 42 0.030
1133
CRB132 Cerebral Sinovenous Thrombosis 42 0.030
1134
PRV003 Perivascular Epithelioid Cell Tumor 42 0.030
1135
c ACQ012 Acquired Angioedema 42 0.030
1136
BRS079 Breast Cancer, Protection Against 42 0.030
1137
MNN034 Mannose-Binding Lectin Deficiency 41 0.030
1138
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 41 0.030
1139
WRN003 Wernicke Encephalopathy 41 0.030
1140
PLN006 Poland Syndrome 41 0.030
1141
INP001 Inappropriate Adh Syndrome 41 0.030
1142
GST071 Gastrointestinal Carcinoma 40 0.030
1143
GNG006 Gingival Hypertrophy 40 0.030
1144
ENT007 Enteropathica 40 0.030
1145
EPD053 Epidermal Nevus, Somatic 39 0.030
1146
PTY004 Pityriasis Lichenoides 39 0.030
1147
HPT063 Hepatitis B Virus Infection 39 0.030
1148
MLG065 Malignant Fibroxanthoma 39 0.030
1149
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 39 0.030
1150
c HVY001 Heavy Chain Disease 39 0.030
1151
GST012 Gastroesophageal Junction Adenocarcinoma 39 0.030
1152
c MLR021 Malaria, Severe 39 0.030
1153
GST020 Gastric Antral Vascular Ectasia 39 0.030
1154
CHL056 Cheilitis 39 0.030
1155
CMB021 Combined Pituitary Hormone Deficiency 38 0.030
1156
IRD001 Iridocyclitis 38 0.030
1157
ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 38 0.030
1158
P HYP071 Hypersensitivity Reaction Type Ii Disease 37 0.030
1159
FTD001 Foot Drop 37 0.030
1160
P GMM003 Gamma Heavy Chain Disease 37 0.030
1161
GTT002 Guttate Psoriasis 37 0.030
1162
TST004 Testicular Lymphoma 37 0.030
1163
SZR001 Sezary's Disease 37 0.030
1164
P RNG004 Ring Chromosome 1 36 0.030
1165
c JVN009 Juvenile Pilocytic Astrocytoma 36 0.030
1166
OPT006 Optic Nerve Disease 36 0.030
1167
ATY005 Atypical Teratoid Rhabdoid Tumor 36 0.030
1168
CHR415 Chronic Venous Leg Ulcers 36 0.030
1169
PTT021 Pituitary Hormone Deficiency, Combined 2 36 0.030
1170
SPP002 Sipple Syndrome 35 0.030
1171
KLD001 Keloids 34 0.030
1172
DYS012 Dyshidrosis 34 0.030
1173
NCR009 Necrobiotic Xanthogranuloma 34 0.030
1174
BLD087 Bladder Cancer, Somatic 34 0.030
1175
NVS013 Nevus Sebaceous, Somatic 34 0.030
1176
P LNG038 Lung Small Cell Carcinoma 33 0.030
1177
ENG004 Engraftment Syndrome 33 0.030
1178
CRV036 Cervical Carcinosarcoma 33 0.030
1179
TRC006 Trichosporonosis 32 0.030
1180
CHL040 Cholangiolocellular Carcinoma 32 0.030
1181
c RHB009 Rhabdomyosarcoma 2, Alveolar 32 0.030
1182
BRG002 Berger Disease 32 0.030
1183
TST021 Testicular Germ Cell Tumor 31 0.030
1184
c CHR091 Chronic Meningitis 31 0.030
1185
CNG058 Congenital Antithrombin Deficiency Type 3 31 0.030
1186
RMS005 Ramsay-Hunt Syndrome 29 0.030
1187
P PLM064 Pulmonary Sequestration 29 0.030
1188
c ACQ010 Acquired Polycythemia 29 0.030
1189
c RNG022 Ring Chromosome 6 29 0.030
1190
CNG028 Congenital Hypoplastic Anemia 28 0.030
1191
LCH007 Lichen Planus Follicularis 27 0.030
1192
MRL001 Meralgia Paresthetica 26 0.030
1193
STR019 Steroid-Induced Glaucoma 26 0.030
1194
JBR008 Juberg-Hayward Syndrome 26 0.030
1195
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 26 0.030
1196