Search results for "leukemia"

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

2333 hits were found for 'leukemia'

# Family MCID Name MIFTS Score
1
c MYL006 Myeloid Leukemia 74 7.632
2
P LKM002 Leukemia 76 7.425
3
P CHR090 Chronic Lymphocytic Leukemia 88 6.523
4
c CHR065 Chronic Myeloid Leukemia 73 5.814
5
P ACT019 Acute Myeloid Leukemia 92 5.457
6
ACT095 Acute Biphenotypic Leukemia 54 4.744
7
ACT119 Acute Promyelocytic Leukemia 68 4.614
8
P ACT101 Acute Lymphoblastic Leukemia 64 4.579
9
P JVN004 Juvenile Myelomonocytic Leukemia 70 4.102
10
MGK001 Megakaryocytic Leukemia 56 4.100
11
P ACT020 Acute T Cell Leukemia 40 4.094
12
c ACT073 Acute Leukemia 56 4.019
13
NTR003 Natural Killer Cell Leukemia 56 3.889
14
P ACT009 Acute Monocytic Leukemia 56 3.824
15
c ADL017 Adult T-Cell Leukemia 45 3.683
16
c ACT115 Acute Myeloid Leukemia, Adult 54 3.679
17
c LYM026 Lymphoblastic Leukemia 56 3.634
18
c TCL004 T-Cell Leukemia 50 3.505
19
HRY003 Hairy Cell Leukemia 58 3.445
20
c ACT074 Acute Lymphocytic Leukemia 69 3.408
21
c CHR285 Chronic Myelomonocytic Leukemia 55 3.314
22
TCL002 T-Cell Large Granular Lymphocyte Leukemia 47 3.286
23
ACT098 Acute Erythroid Leukemia 44 3.219
24
c ACT117 Acute Myelomonocytic Leukemia 54 3.186
25
c MNC007 Monocytic Leukemia 56 3.152
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 2.922
29
LRG008 Large Granular Lymphocyte Leukemia 39 2.919
30
ACT200 Acute Monoblastic Leukemia 49 2.891
31
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.831
32
PRL017 Prolymphocytic Leukemia 43 2.799
33
c LKM060 Leukemia, Acute Lymphoblastic 3 47 2.799
34
PLS016 Plasma Cell Leukemia 48 2.798
35
c SBC004 Subacute Myeloid Leukemia 22 2.773
36
CHL061 Childhood Leukemia 38 2.729
37
CNT018 Central Nervous System Leukemia 41 2.728
38
P BCL005 B Cell Prolymphocytic Leukemia 24 2.657
39
c LKM005 Leukemia, T-Cell, Chronic 17 2.617
40
c TCL005 T-Cell Prolymphocytic Leukemia 49 2.597
41
CHR286 Chronic Neutrophilic Leukemia 48 2.581
42
ACT103 Acute Lymphoblastic Leukemia, Childhood 14 2.562
43
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 14 2.562
44
NNN018 Noonan-Like Syndrome Disorder with or Without Juvenile Myelomonocytic Leukemia 25 2.535
45
c SYS004 Systemic Mastocytosis 64 2.482
46
SBL003 Subleukemic Leukemia 13 2.360
47
HCL001 Hcl-V 31 2.344
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 19 2.172
53
ACT113 Acute Myeloblastic Leukemia with Maturation 34 2.134
54
c CHR064 Chronic Monocytic Leukemia 22 2.127
55
ACT114 Acute Myeloblastic Leukemia Without Maturation 28 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 2.048
62
MST002 Mast-Cell Leukemia 35 1.997
63
ACT118 Acute Non Lymphoblastic Leukemia 24 1.988
64
c CHR418 Chronic Leukemia 37 1.974
65
ALK003 Aleukemic Leukemia Cutis 20 1.946
66
ACT177 Acute Basophilic Leukemia 38 1.944
67
P PRB001 Pre-B-Cell Acute Lymphoblastic Leukemia 39 1.926
68
P LFR001 Li-Fraumeni Syndrome 88 1.904
69
RFR002 Refractory Hairy Cell Leukemia 14 1.873
70
ACT097 Acute Erythroblastic Leukemia 12 1.873
71
NNT007 Neonatal Leukemia 22 1.859
72
c SBC006 Subacute Leukemia 12 1.836
73
FML083 Familial Platelet Disorder with Associated Myeloid Malignancy 27 1.822
74
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 12 1.822
75
LKM036 Leukemia, Acute Nonlymphocytic 10 1.817
76
ALK002 Aleukemic Monocytic Leukemia Cutis 9 1.817
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 13 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 39 1.615
90
c FML114 Familial Chronic Lymphocytic Leukemia 37 1.599
91
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 27 1.548
92
c 8P1002 8p11 Myeloproliferative Syndrome 37 1.538
93
CLL014 Cll/sll 30 1.538
94
MYL050 Myeloid Leukemia, Acute, M4/m4eo Subtype, Somatic 35 1.530
95
P ACT208 'acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation' 30 1.530
96
LKM016 Leukemia, Acute Myeloid, Somatic 35 1.527
97
LKM017 Leukemia, Acute Myeloid, Reduced Survival in 35 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)' 13 1.488
115
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 11 1.488
116
LKM023 Leukemia, Myeloid/lymphoid or Mixed-Lineage 10 1.488
117
P LKM024 Leukemia/lymphoma, T-Cell 11 1.481
118
BLN016 Bilineal Acute Leukemia 10 1.481
119
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 8 1.481
120
c HMN023 Human T-Cell Leukemia Virus Type 3 7 1.481
121
c MYL018 Myelocytic Leukemia-Like Syndrome, Familial, Chronic 5 1.481
122
ACT116 Acute Myeloid Leukemia, Childhood 4 1.481
123
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 5 1.474
124
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 10 1.466
125
MGK006 'megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13)' 10 1.466
126
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 8 1.466
127
c LKM010 Leukemia/lymphoma, B-Cell, 3 7 1.466
128
c FML115 Familial Chronic Myelocytic Leukemia 5 1.466
129
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 2 1.466
130
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 11 1.457
131
c LKM008 Leukemia, Acute Pre-B-Cell 10 1.457
132
c NPM001 Npm1-Related Acute Myeloid Leukemia 10 1.457
133
HRY001 Hairy Cell Leukemia of Spleen 9 1.457
134
LKM026 Leukemia, Acute Myeloid, Therapy-Related 8 1.457
135
c LKM050 Leukemia, Chronic Lymphocytic 1 8 1.457
136
c LKM051 Leukemia, Chronic Lymphocytic 3 8 1.457
137
c LKM052 Leukemia, Chronic Lymphocytic 5 8 1.457
138
c LKM053 Leukemia, Chronic Lymphocytic 4 8 1.457
139
c LKM054 Leukemia, Acute Lymphocytic 1 8 1.457
140
c LKM056 Leukemia, Chronic Lymphocytic 2 8 1.457
141
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 8 1.457
142
ACT204 'acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2)' 8 1.457
143
c LKM055 Leukemia, Acute Lymphoblastic 2 7 1.457
144
c LYM061 Lymphocytic Leukemia, Acute T-Cell 7 1.457
145
c LKM009 Leukemia/lymphoma, B-Cell, 2 6 1.457
146
LKM018 Leukemia, T-Cell Acute Lymphoblastoid 6 1.457
147
BND002 B- and T-Cell Mixed Leukemia 6 1.457
148
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 6 1.457
149
CLS019 Classic Mast Cell Leukemia 6 1.457
150
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 5 1.457
151
LKM020 Leukemia, Acute Myeloid, with Eosinophilia 5 1.457
152
TCL013 T-Cell Prolymphocytic Leukemia, Somatic 5 1.457
153
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 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
AZT002 Azathioprine Dose Selection in the Treatment of Crohn Disease, Leukemia and in Transplantation 3 1.457
165
LKM034 Leukemia, Transient, of Down Syndrome 3 1.457
166
MRC007 Mercaptopurine Dose Selection in the Treatment of Crohn Disease, Leukemia and in Transplantation 3 1.457
167
LYM040 Lymphoblastic Lymphoma 53 1.316
168
P HYP098 Hypereosinophilic Syndrome 61 1.199
169
P FML045 Familial Mosaic Monosomy 7 Syndrome 17 1.104
170
EMB016 Emberger Syndrome 27 1.085
171
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 22 1.079
172
NSY001 N Syndrome 34 1.052
173
WTL001 Wt Limb Blood Syndrome 24 1.043
174
MYL040 Myelodysplastic Syndromes 79 0.308
175
HMT018 Hematopoietic Stem Cell Transplantation 40 0.219
176
c MYL007 Myeloma 60 0.194
177
SRC014 Sarcoma 68 0.187
178
END072 Endotheliitis 50 0.169
179
P MLT019 Multiple Myeloma 88 0.164
180
DWN001 Down Syndrome 61 0.151
181
P GRF002 Graft Versus Host Disease 64 0.150
182
P MYL005 Myelofibrosis 74 0.147
183
P WLM002 Wilms Tumor 66 0.141
184
HDG007 Hodgkin's Lymphoma 93 0.140
185
c NTR004 Neutropenia 65 0.138
186
THR013 Thoracic Outlet Syndrome 52 0.136
187
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.136
188
P BCL006 B-Cell Lymphomas 56 0.132
189
P MST009 Mastocytosis 75 0.131
190
c HPT021 Hepatitis 63 0.131
191
SYN053 Syndromic Diarrhea 34 0.131
192
MYL003 Myeloid Sarcoma 55 0.130
193
LYM019 Lymphosarcoma 58 0.129
194
P BRS047 Breast Cancer 85 0.126
195
c HML002 Hemolytic Anemia 65 0.124
196
HYP004 Hypercalcemia 64 0.124
197
P ESN007 Eosinophilia 62 0.123
198
RFR010 Refractory Anemia 50 0.121
199
BRK003 Burkitt's Lymphoma 77 0.120
200
NNH001 Non-Hodgkin Lymphoma 72 0.120
201
P ATX002 Ataxia Telangiectasia 87 0.117
202
P HST010 Histiocytosis 63 0.116
203
ANK002 Ankylosing Spondylitis 76 0.113
204
P ATM010 Autoimmune Hemolytic Anemia 66 0.113
205
c BNG076 Benign Exophthalmos Syndrome 22 0.112
206
P ANG001 Angelman Syndrome 71 0.111
207
ART019 Aortic Valve Stenosis 63 0.111
208
P RHM011 Rheumatoid Arthritis 94 0.110
209
ACN002 Acanthosis Nigricans 64 0.110
210
P ATX010 Ataxia Neuropathy Spectrum 47 0.109
211
P ART022 Arthritis 74 0.108
212
P APL001 Aplastic Anemia 84 0.105
213
c THR014 Thrombocytopenia 69 0.104
214
PRS047 Prostatitis 59 0.104
215
PLY001 Polycythemia Vera 85 0.103
216
SVR004 Severe Combined Immunodeficiency 78 0.103
217
c MNN013 Meningitis 67 0.103
218
c PLY018 Polycythemia 59 0.103
219
PRR002 Pure Red-Cell Aplasia 55 0.103
220
c ESS003 Essential Thrombocythemia 61 0.102
221
RCH001 Richter's Syndrome 35 0.102
222
ASP006 Aspergillosis 72 0.100
223
DSS009 Disseminated Intravascular Coagulation 61 0.100
224
LKS001 Leukostasis 49 0.100
225
P NRF002 Neurofibromatosis 94 0.099
226
P PNM007 Pneumonia 77 0.099
227
BNM005 Bone Marrow Necrosis 39 0.099
228
VSC011 Vasculitis 65 0.098
229
c THY032 Thyroiditis 65 0.096
230
SPS019 Spastic Paraparesis 40 0.096
231
SPS057 Spasticity 37 0.096
232
MNT001 Mantle Cell Lymphoma 64 0.095
233
c HMP002 Hemophagocytic Lymphohistiocytosis 59 0.095
234
AND002 Androgen Insensitivity Syndrome 80 0.094
235
c AXN002 Axenfeld-Rieger Syndrome 69 0.094
236
THR004 Thrombocytosis 60 0.094
237
CRB009 Cerebritis 38 0.094
238
GLC037 Glucocorticoid Resistance 52 0.092
239
TRP002 Tropical Spastic Paraparesis 55 0.091
240
MCR004 Macroglobulinemia 54 0.091
241
c NNN003 Noonan Syndrome 79 0.090
242
TTR011 Tetraploidy 61 0.090
243
RTN023 Retinitis 53 0.090
244
P LVR011 Liver Cancer 90 0.089
245
NRP001 Neuropathy 61 0.089
246
P RTN024 Retinoblastoma 83 0.087
247
P FNC001 Fanconi's Anemia 65 0.087
248
ART001 Arterial Tortuosity Syndrome 55 0.087
249
AND003 Andersen-Tawil Syndrome 53 0.087
250
LKM001 Leukemoid Reaction 48 0.087
251
c MLG054 Malignant Histiocytosis 62 0.086
252
DPH001 Diphtheria 57 0.086
253
c SVR003 Severe Congenital Neutropenia 54 0.086
254
MDS022 Mediastinitis 45 0.085
255
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.085
256
TFT003 Tufting Enteropathy 28 0.085
257
c ATX004 Ataxia 58 0.083
258
P DBT005 Diabetes Insipidus 57 0.083
259
BCT015 Bacteremia 49 0.083
260
P PNC001 Pancytopenia 48 0.083
261
P MLN008 Melanoma 64 0.082
262
c ACT135 Acute Graft Versus Host Disease 49 0.082
263
PRP030 Purpura 65 0.081
264
c ACR001 Aicardi-Goutieres Syndrome 54 0.079
265
P LNG032 Lung Cancer 78 0.078
266
HMT002 Hematologic Cancer 62 0.078
267
SMT015 Smith Magenis Syndrome 58 0.078
268
HYP266 Hypoxia 57 0.078
269
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 54 0.078
270
P PRS040 Prostate Cancer 97 0.076
271
P GLM007 Glomerulonephritis 68 0.076
272
LNG024 Langerhans-Cell Histiocytosis 57 0.076
273
GRN017 Granulocytopenia 46 0.076
274
c CHR417 Chronic Graft Versus Host Disease 42 0.076
275
P MLT020 Multiple Sclerosis 84 0.075
276
P NRB001 Neuroblastoma 70 0.075
277
c PNC044 Pancreatitis 68 0.075
278
P INF038 Influenza 67 0.075
279
GNG013 Gingivitis 60 0.075
280
DFF005 Diffuse Large B-Cell Lymphoma 55 0.075
281
HMG002 Hemoglobinuria 51 0.075
282
SPL018 Splenomegaly 46 0.075
283
BLS007 Blastic Plasmacytoid Dendritic Cell 44 0.075
284
CHR066 Chronic Fatigue Syndrome 65 0.073
285
MYC002 Mycobacterium Avium Complex Disease 58 0.073
286
HST016 Histiocytic Sarcoma 51 0.073
287
ZYG002 Zygomycosis 44 0.073
288
HV1006 Hiv-1 63 0.072
289
P ADN016 Adenocarcinoma 58 0.072
290
INV001 Invasive Aspergillosis 52 0.072
291
EMN001 Emanuel Syndrome 41 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 89 0.070
297
P HYP075 Hypertension 85 0.070
298
MYC006 Mycosis Fungoides 68 0.070
299
P HRP006 Herpes Simplex 66 0.070
300
c CND004 Candidiasis 61 0.070
301
P PLY019 Polyneuropathy 60 0.070
302
P PLM006 Pulmonary Alveolar Proteinosis 52 0.070
303
c CNT035 Central Nervous System Disease 48 0.070
304
c HPT016 Hepatitis B 68 0.069
305
ABT001 Abetalipoproteinemia 66 0.069
306
P ANP001 Anaplastic Large Cell Lymphoma 62 0.069
307
P THR090 Thrombocythemia 1 58 0.069
308
OST003 Osteonecrosis 58 0.069
309
BNM001 Bone Marrow Cancer 54 0.069
310
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.069
311
IPX001 Ipex Syndrome 36 0.069
312
TBR010 Tuberculosis 85 0.067
313
P SRC013 Sarcoidosis 73 0.067
314
P NJM001 Nijmegen Breakage Syndrome 70 0.067
315
SPS077 Sepsis 69 0.067
316
P HPT001 Hepatitis C 66 0.067
317
DRM006 Dermatitis 65 0.067
318
URT039 Urticaria 63 0.067
319
CTN014 Cutaneous Mastocytosis 58 0.067
320
NRN002 Neuronitis 43 0.067
321
P MNN012 Meningioma 78 0.065
322
c PRP029 Porphyria 67 0.065
323
MGL001 Megaloblastic Anemia 65 0.065
324
DFC004 Deficiency Anemia 62 0.065
325
HRP004 Herpes Zoster 57 0.065
326
HPT023 Hepatocellular Carcinoma 54 0.065
327
BLN003 Blindness 52 0.065
328
RTC005 Reticulosarcoma 43 0.065
329
FLL019 Follicular Mucinosis 39 0.065
330
P RFR008 Refractory Anemia with Excess Blasts 33 0.065
331
FSR001 Fusariosis 28 0.065
332
MN1001 Mn1 21 0.065
333
P FRD001 Friedreich Ataxia 70 0.064
334
c UVT001 Uveitis 65 0.064
335
P FTL006 Fetal Alcohol Spectrum Disorder 60 0.064
336
RHB003 Rhabdomyosarcoma 58 0.064
337
P CRV039 Cervicitis 57 0.064
338
P JVN003 Juvenile Xanthogranuloma 53 0.064
339
LKP004 Leukopenia 44 0.064
340
P SDR003 Sideroblastic Anemia 43 0.064
341
P SYS001 Systemic Lupus Erythematosus 89 0.062
342
P GST019 Gastrointestinal Stromal Tumor 83 0.062
343
P RBN001 Rubinstein-Taybi Syndrome 77 0.062
344
GLN003 Glanzmann's Thrombasthenia 76 0.062
345
P PRP003 Porphyria Cutanea Tarda 75 0.062
346
c LPS004 Lupus Erythematosus 75 0.062
347
CLT003 Colitis 64 0.062
348
P RNL014 Renal Cell Carcinoma 63 0.062
349
HYP066 Hyperglycemia 61 0.062
350
PMP001 Pemphigus 59 0.062
351
P GLB002 Glioblastoma 58 0.062
352
HYP063 Hypersplenism 58 0.062
353
PRC012 Pericardial Effusion 57 0.062
354
P PRP023 Peripheral Neuropathy 51 0.062
355
PLS025 Plasmablastic Lymphoma 51 0.062
356
OST019 Osteosclerosis 51 0.062
357
HYP025 Hyperphosphatemia 43 0.062
358
GRF001 Graft-Versus-Host Disease, Protection Against 31 0.062
359
c TTR021 Tetrasomy 21 29 0.062
360
P FML018 Familial Mediterranean Fever 75 0.060
361
c DBT009 Diabetes Mellitus 73 0.060
362
P RSP003 Respiratory Failure 68 0.060
363
c AMY001 Amyotrophic Lateral Sclerosis 66 0.060
364
IDP064 Idiopathic Neutropenia 62 0.060
365
c KBK001 Kabuki Syndrome 56 0.060
366
P PND001 Pain Disorder 54 0.060
367
P CHR092 Chronic Myeloproliferative Disease 49 0.060
368
PYM001 Pyomyositis 48 0.060
369
c HPT073 Hepatitis C Virus 47 0.060
370
P FLL037 Follicular Lymphoma 47 0.060
371
PRM041 Primary Cortisol Resistance 21 0.060
372
INF030 Infectious Mononucleosis 84 0.058
373
CRH001 Crohn's Disease 75 0.058
374
P AMY004 Amyloidosis 73 0.058
375
c PRM002 Primary Hyperoxaluria 73 0.058
376
P AST007 Astrocytoma 72 0.058
377
GLL008 Gilles De La Tourette Syndrome 72 0.058
378
P CLN016 Colon Cancer 64 0.058
379
SCB001 Scabies 60 0.058
380
PLS011 Plasmacytoma 56 0.058
381
P CTN015 Cutaneous T Cell Lymphoma 51 0.058
382
GRM009 Germ Cell Tumors 49 0.058
383
HYP017 Hypophosphatemia 48 0.058
384
LCT001 Lactic Acidosis 47 0.058
385
DND018 Dendritic Cell Tumor 47 0.058
386
URT008 Urticaria Pigmentosa 46 0.058
387
CYT008 Cytomegalovirus Infection 43 0.058
388
VRL011 Viral Infectious Disease 38 0.058
389
ATM004 Autoimmune Thrombocytopenic Purpura 69 0.056
390
c ENC004 Encephalitis 65 0.056
391
P PTT014 Pitt-Hopkins Syndrome 59 0.056
392
CLL003 Cellulitis 58 0.056
393
PSD002 Pseudotumor Cerebri 56 0.056
394
PRT011 Protein C Deficiency 55 0.056
395
KLN001 Klinefelter's Syndrome 55 0.056
396
AGG002 Aggressive Systemic Mastocytosis 52 0.056
397
EWN002 Ewing's Family of Tumors 50 0.056
398
SFT003 Soft Tissue Sarcoma 49 0.056
399
LYM051 Lymphomatoid Granulomatosis 48 0.056
400
BCK006 Back Pain 38 0.056
401
3Q2002 3q21q26 Syndrome 28 0.056
402
ECT004 Ecthyma 27 0.056
403
P MYC007 Myocardial Infarction 92 0.054
404
ADN001 Adenosine Deaminase Deficiency 73 0.054
405
P THY023 Thymoma 68 0.054
406
P HYP117 Hypertriglyceridemia 67 0.054
407
BRN028 Brain Cancer 64 0.054
408
FLT001 Felty's Syndrome 64 0.054
409
c ACT027 Acute Pancreatitis 63 0.054
410
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.054
411
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.054
412
P SNS014 Sinusitis 57 0.054
413
P END033 Endocarditis 56 0.054
414
THY009 Thyroid Lymphoma 53 0.054
415
MNN014 Mononeuritis 51 0.054
416
P NRV007 Nervous System Disease 49 0.054
417
HYP005 Hypokalemia 49 0.054
418
EVN001 Evans' Syndrome 45 0.054
419
5QS001 5q- Syndrome 45 0.054
420
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.054
421
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 38 0.054
422
c LYM034 Lymphoproliferative Disease, X-Linked 29 0.054
423
c HRD009 Hereditary Wilms' Tumor 22 0.054
424
P RTT002 Rett Syndrome 83 0.052
425
P OST018 Osteosarcoma 81 0.052
426
P PLL001 Pallister-Hall Syndrome 72 0.052
427
P RTH001 Rothmund-Thomson Syndrome 70 0.052
428
P NNN008 Noonan Syndrome 1 68 0.052
429
MSL001 Measles 67 0.052
430
P OLG002 Oligodendroglioma 62 0.052
431
MLL005 Miller-Dieker Syndrome 62 0.052
432
BRN002 Bronchiolitis 60 0.052
433
PRP007 Priapism 59 0.052
434
BRN012 Bronchiolitis Obliterans 59 0.052
435
PLY041 Polymyositis 58 0.052
436
PRT039 Proteinuria 57 0.052
437
ACT100 Acute Febrile Neutrophilic Dermatosis 57 0.052
438
TNS005 Tonsillitis 56 0.052
439
CYT005 Cytomegalovirus Retinitis 56 0.052
440
P EXN002 Exanthem 55 0.052
441
APP008 Appendicitis 55 0.052
442
P INF032 Infertility 54 0.052
443
PRM163 Primary Mediastinal Large B-Cell Lymphoma 52 0.052
444
GRN007 Granuloma Annulare 52 0.052
445
CLN015 Colon Adenocarcinoma 52 0.052
446
PRN049 Paraneoplastic Pemphigus 50 0.052
447
PRP036 Peripheral T-Cell Lymphoma 48 0.052
448
P MLG081 Malignant Teratoma 47 0.052
449
P HML001 Hemolytic-Uremic Syndrome 47 0.052
450
MMB001 Membranoproliferative Glomerulonephritis 47 0.052
451
PNN001 Panniculitis 46 0.052
452
DNR001 Duane Retraction Syndrome 45 0.052
453
ANP009 Anaplastic Oligodendroglioma 42 0.052
454
P DNS004 Duane Syndrome Type 2 40 0.052
455
SPL006 Splenic Infarction 38 0.052
456
TRS012 Trisomy 22 30 0.052
457
ACT176 Acute Panmyelosis with Myelofibrosis 22 0.052
458
OTP003 Oto-Palatal-Digital Syndrome 17 0.052
459
P CLR023 Colorectal Cancer 77 0.050
460
P LPR002 Leopard Syndrome 75 0.050
461
P MYS005 Myositis 71 0.050
462
c CWD001 Cowden Disease 71 0.050
463
c THL005 Thalassemia 71 0.050
464
PYR013 Pyruvate Kinase Deficiency 68 0.050
465
c NPH012 Nephrotic Syndrome 67 0.050
466
P AVS004 Avascular Necrosis of the Femoral Head 60 0.050
467
P LPS002 Liposarcoma 60 0.050
468
VNS009 Venous Thrombosis 59 0.050
469
c TRT010 Teratoma 58 0.050
470
CRY004 Cryoglobulinemia 58 0.050
471
MRK001 Merkel Cell Carcinoma 55 0.050
472
PRN011 Pernicious Anemia 55 0.050
473
PLY020 Polyradiculoneuropathy 54 0.050
474
CRD001 Cardiac Tamponade 54 0.050
475
c CPL003 Capillary Leak Syndrome 52 0.050
476
TLN003 Telangiectasis 49 0.050
477
GLM011 Glomerulosclerosis 47 0.050
478
LYM045 Lymphocytic Vasculitis 47 0.050
479
SPN060 Spondylocarpotarsal Synostosis Syndrome 44 0.050
480
FCT013 Factor V Leiden Thrombophilia 34 0.050
481
c TCL008 T-Cell Lymphoma 1a 12 0.050
482
P ALZ001 Alzheimer's Disease 98 0.047
483
KPS001 Kaposi's Sarcoma 86 0.047
484
P HMC003 Hemochromatosis 85 0.047
485
BLM001 Bloom Syndrome 74 0.047
486
SHW002 Shwachman-Diamond Syndrome 69 0.047
487
THR079 Thromboembolism 67 0.047
488
MLT022 Malt Lymphoma 62 0.047
489
c AGM001 Agammaglobulinemia 61 0.047
490
SPT013 Septic Shock 60 0.047
491
DNG003 Dengue Disease 59 0.047
492
NRC020 Neuroectodermal Tumor 59 0.047
493
MYX005 Myxoid Liposarcoma 59 0.047
494
P MMP001 Mumps 59 0.047
495
NTR001 Neutral Lipid Storage Disease 59 0.047
496
EXT010 Extramedullary Plasmacytoma 58 0.047
497
OST017 Osteomyelitis 58 0.047
498
NRH001 Neurohypophyseal Diabetes Insipidus 57 0.047
499
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 56 0.047
500
PYD001 Pyoderma Gangrenosum 56 0.047
501
DND002 Dendritic Cell Sarcoma 55 0.047
502
PST062 Pustulosis Palmaris Et Plantaris 53 0.047
503
c ACT134 Acute Liver Failure 53 0.047
504
PYD002 Pyoderma 51 0.047
505
LYM027 Lymphopenia 50 0.047
506
PRT026 Parotitis 49 0.047
507
c MSB002 Mesoblastic Nephroma 49 0.047
508
P CNG029 Congenital Mesoblastic Nephroma 47 0.047
509
GYN001 Gynecomastia 45 0.047
510
NRG004 Neurogenic Diabetes Insipidus 42 0.047
511
EPG003 Epiglottitis 41 0.047
512
ANG046 Angioimmunoblastic T-Cell Lymphoma 39 0.047
513
SPR035 Superior Vena Cava Syndrome 39 0.047
514
c SRC025 Sarcoidosis 1 39 0.047
515
GST053 Gastric Cancer 38 0.047
516
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 32 0.047
517
CYT004 Cytomegalic Inclusion Disease 29 0.047
518
ACQ031 Acquired Idiopathic Sideroblastic Anemia 28 0.047
519
IRN002 Iron Metabolism Disease 27 0.047
520
HPT070 Hepatosplenic T-Cell Lymphoma 26 0.047
521
CD4007 Cd4+/cd56+ Hematodermic Neoplasm 25 0.047
522
c RNG017 Ring Chromosome 21 24 0.047
523
P MDL005 Medulloblastoma 80 0.045
524
P PRM021 Primary Pulmonary Hypertension 80 0.045
525
THY028 Thyroid Cancer 74 0.045
526
P CHR071 Charcot-Marie-Tooth Disease 73 0.045
527
P FCL005 Focal Segmental Glomerulosclerosis 72 0.045
528
ACQ007 Acquired Immunodeficiency Syndrome 70 0.045
529
P KDN017 Kidney Cancer 69 0.045
530
ANT006 Antiphospholipid Syndrome 68 0.045
531
c JVN010 Juvenile Rheumatoid Arthritis 67 0.045
532
P HYP056 Hypoglycemia 66 0.045
533
STR008 Strongyloidiasis 65 0.045
534
c HMP007 Hemophilia 64 0.045
535
P LRY019 Laryngitis 64 0.045
536
P MYP004 Myopathy 61 0.045
537
CHL067 Cholecystitis 60 0.045
538
P END047 Endophthalmitis 59 0.045
539
CLD007 Cold Agglutinin Disease 59 0.045
540
PPL002 Papillary Carcinoma 58 0.045
541
RTN017 Retinal Detachment 56 0.045
542
P THR012 Thoracic Cancer 54 0.045
543
NRF008 Neurofibromatosis-Noonan Syndrome 53 0.045
544
PRC013 Pericarditis 52 0.045
545
GRW007 Growth Hormone Deficiency 52 0.045
546
OBS001 Obstructive Jaundice 50 0.045
547
RTN001 Retinal Vasculitis 50 0.045
548
P ALV004 Alveolar Rhabdomyosarcoma 49 0.045
549
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 47 0.045
550
LYM021 Lymphadenitis 47 0.045
551
LKP003 Leukoplakia 45 0.045
552
ANR040 Aneurysm 45 0.045
553
THR035 Thrombasthenia 44 0.045
554
MLG083 Male Germ Cell Tumor 44 0.045
555
TST015 Testicular Disease 41 0.045
556
ANG037 Angiomatosis 38 0.045
557
NRW001 Norwegian Scabies 34 0.045
558
PNM003 Pneumatosis Cystoides Intestinalis 25 0.045
559
RFR007 Refractory Anemia with Excess Blasts in Transformation 20 0.045
560
GLC006 Galactosemia 85 0.042
561
c BTT002 Beta Thalassemia 82 0.042
562
P MYS003 Myasthenia Gravis 79 0.042
563
SKN016 Skin Disease 74 0.042
564
c PLM037 Pulmonary Hypertension 73 0.042
565
P TMP003 Temporal Arteritis 72 0.042
566
c JBR001 Joubert Syndrome 69 0.042
567
P MLG075 Malignant Mesothelioma 68 0.042
568
P BCK002 Beckwith-Wiedemann Syndrome 68 0.042
569
ACT049 Acute Disseminated Encephalomyelitis 66 0.042
570
P ATM006 Autoimmune Lymphoproliferative Syndrome 66 0.042
571
ADN018 Adenoma 65 0.042
572
P INS005 Insulin Resistance 64 0.042
573
ULC004 Ulcerative Colitis 64 0.042
574
P FBR017 Fibrosarcoma 63 0.042
575
c HRD010 Hereditary Spastic Paraplegia 63 0.042
576
c HYP076 Hyperthyroidism 62 0.042
577
SCK005 Sickle Cell Disease 61 0.042
578
P LMY004 Leiomyosarcoma 61 0.042
579
c ALM001 Al Amyloidosis 60 0.042
580
GLL022 Guillain-Barre Syndrome 60 0.042
581
PST046 Post-Transplant Lymphoproliferative Disease 59 0.042
582
CHC001 Chickenpox 59 0.042
583
c ACT075 Acute Myocardial Infarction 59 0.042
584
P PRM011 Primary Ciliary Dyskinesia 58 0.042
585
MRG003 Marginal Zone B-Cell Lymphoma 58 0.042
586
P JBR004 Joubert Syndrome 2 57 0.042
587
FLL008 Folliculitis 57 0.042
588
ORL005 Oral Candidiasis 57 0.042
589
PLM020 Pleomorphic Xanthoastrocytoma 57 0.042
590
c CNT016 Central Retinal Vein Occlusion 57 0.042
591
LRY018 Laryngeal Squamous Cell Carcinoma 57 0.042
592
c HRD001 Hereditary Multiple Exostoses 56 0.042
593
c PST005 Posterior Uveitis 56 0.042
594
BLS002 Blastomycosis 56 0.042
595
P FNC025 Fanconi Anemia, Complementation Group J 55 0.042
596
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 55 0.042
597
NCR004 Nocardiosis 55 0.042
598
CRD005 Cardia Cancer 55 0.042
599
GST050 Gastrointestinal System Disease 55 0.042
600
CHR008 Choroiditis 53 0.042
601
SPT004 Septic Arthritis 53 0.042
602
STN007 Stenotrophomonas Maltophilia 52 0.042
603
RSC001 Rosacea 52 0.042
604
c ACQ014 Acquired Hemophilia 51 0.042
605
RPP001 Rapp-Hodgkin Syndrome 50 0.042
606
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 50 0.042
607
THY022 Thymic Carcinoma 49 0.042
608
GNG002 Ganglioneuroma 48 0.042
609
GLM037 Glioma Somatic 47 0.042
610
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.042
611
c DMY001 Demyelinating Polyneuropathy 46 0.042
612
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 45 0.042
613
ILS001 Ileus 44 0.042
614
TCL003 T Cell Deficiency 44 0.042
615
c HRD086 Hereditary Hypophosphatemic Rickets 43 0.042
616
HPT022 Hepatoblastoma 43 0.042
617
SPR033 Superficial Spreading Melanoma 43 0.042
618
P LSS005 Lissencephaly 1 42 0.042
619
CMP001 Composite Lymphoma 38 0.042
620
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 38 0.042
621
HMR023 Hemorrhagic Cystitis 38 0.042
622
IMM088 Immunodeficiency 36 36 0.042
623
PRL008 Paralytic Ileus 36 0.042
624
BLT011 Bilateral Perisylvian Polymicrogyria 34 0.042
625
CHR020 Chronic Interstitial Cystitis 33 0.042
626
CLC008 Colchicine Resistance 31 0.042
627
MTR008 Mature B-Cell Neoplasm 31 0.042
628
SPL007 Splenic Abscess 30 0.042
629
c DYS055 Dystonia 10 27 0.042
630
RHB020 Rhabdomyosarcoma, Somatic 27 0.042
631
HYP179 Hypertrichosis Congenital Generalized X-Linked 26 0.042
632
EXF003 Exfoliative Dermatitis 25 0.042
633
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 21 0.042
634
P GCH001 Gaucher's Disease 83 0.040
635
ESP021 Esophageal Cancer 80 0.040
636
HST011 Histoplasmosis 73 0.040
637
P DRM010 Dermatomyositis 71 0.040
638
P STM004 Stomach Cancer 68 0.040
639
P CRD013 Cardiofaciocutaneous Syndrome 66 0.040
640
HPT002 Hepatic Vein Thrombosis 66 0.040
641
PRP025 Peripheral Primitive Neuroectodermal Tumor 66 0.040
642
GRY002 Gray Platelet Syndrome 63 0.040
643
P ADL010 Adult Respiratory Distress Syndrome 63 0.040
644
P ART023 Arthropathy 63 0.040
645
CMP002 Campylobacteriosis 62 0.040
646
PSR002 Psoriasis 62 0.040
647
c MSC005 Muscular Dystrophy 61 0.040
648
P CNJ013 Conjunctivitis 61 0.040
649
SRS001 Serous Cystadenocarcinoma 60 0.040
650
P SCL015 Scleritis 60 0.040
651
ALP008 Alopecia 59 0.040
652
MLR002 Miliary Tuberculosis 59 0.040
653
c MTH007 Methemoglobinemia 58 0.040
654
c THR005 Thrombotic Thrombocytopenic Purpura 58 0.040
655
ANT009 Antithrombin Iii Deficiency 58 0.040
656
PRN001 Purine Nucleoside Phosphorylase Deficiency 58 0.040
657
END030 End Stage Renal Failure 57 0.040
658
LST001 Listeriosis 57 0.040
659
BRN029 Brain Disease 57 0.040
660
GLB015 Glioblastoma Multiforme 57 0.040
661
P SDR002 Siderosis 57 0.040
662
EPD001 Epidermodysplasia Verruciformis 57 0.040
663
P RPD001 Rapidly Progressive Glomerulonephritis 56 0.040
664
P RTN022 Retinal Vein Occlusion 56 0.040
665
c MNT147 Mental Retardation 56 0.040
666
P CMP008 Compartment Syndrome 55 0.040
667
DDN006 Duodenitis 55 0.040
668
TLP001 Talipes Equinovarus 55 0.040
669
RDC002 Radiculopathy 55 0.040
670
FBR003 Fibrous Histiocytoma 54 0.040
671
HST009 Histiocytoma 54 0.040
672
PTS001 Patau Syndrome 53 0.040
673
HPT032 Hepatocellular Carcinoma, Somatic 53 0.040
674
NPH051 Nephritis 53 0.040
675
ORL011 Oral Cancer 53 0.040
676
TRP014 Triploidy 53 0.040
677
CLC006 Calcinosis 52 0.040
678
HYP037 Hyperhomocysteinemia 52 0.040
679
MLK003 Melkersson-Rosenthal Syndrome 51 0.040
680
ORC001 Orchitis 50 0.040
681
P WLD002 Waldenstrom Macroglobulinemia 50 0.040
682
HYP068 Hyperostosis 50 0.040
683
MCR020 Microsporidiosis 49 0.040
684
OLG006 Oligoastrocytoma 49 0.040
685
c PRM046 Primary Malignant Lymphoma 48 0.040
686
PLR008 Pleurisy 47 0.040
687
PRP016 Paraplegia 47 0.040
688
PRN039 Paraneoplastic Syndromes 46 0.040
689
LYM012 Lymphoplasmacytic Lymphoma 46 0.040
690
PRM097 Primary Immunodeficiency Disease 45 0.040
691
ECT026 Ectopic Pregnancy 45 0.040
692
UTR043 Uterine Sarcoma 45 0.040
693
HDR003 Hidradenitis 43 0.040
694
OLG015 Oligoarticular Juvenile Arthritis 43 0.040
695
MYC017 Mycobacterium Kansasii 41 0.040
696
CDQ001 Cauda Equina Syndrome 41 0.040
697
ACL001 Acalculous Cholecystitis 40 0.040
698
HTL002 Htlv-1 Associated Myelopathy 39 0.040
699
CYC007 Cyclic Thrombocytopenia 38 0.040
700
c HYD008 Hydrocephalus Due to Aqueductal Stenosis 37 0.040
701
INT038 Interdigitating Dendritic Cell Sarcoma 36 0.040
702
BRT011 Bruton-Type Agammaglobulinemia 35 0.040
703
PLY010 Polyclonal Hypergammaglobulinemia 35 0.040
704
MYL013 Myeloperoxidase Deficiency 35 0.040
705
HPT012 Hepatocellular Fibrolamellar Carcinoma 33 0.040
706
NTR005 Nutritional Deficiency Disease 33 0.040
707
MLG041 Malignant Triton Tumor 30 0.040
708
ANP008 Anaplastic Oligoastrocytoma 27 0.040
709
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 22 0.040
710
GNR023 Generalized Eruptive Histiocytosis 22 0.040
711
BLD053 Blood Platelet Disease 21 0.040
712
SML025 Small Non-Cleaved Cell Lymphoma 21 0.040
713
MYL004 Myelodysplastic Myeloproliferative Cancer 20 0.040
714
c CHR257 Chromosome 6q Deletion 19 0.040
715
CYT018 Cytochrome P450 2d6 Variant 16 0.040
716
ALD004 Ala Dehydratase Deficiency 12 0.040
717
INC002 Inclusion Body Myositis 86 0.037
718
SCK003 Sickle Cell Anemia 84 0.037
719
P OVR042 Ovarian Cancer 84 0.037
720
ACR007 Acromegaly 79 0.037
721
P HRD008 Hereditary Hemorrhagic Telangiectasia 76 0.037
722
KWS002 Kawasaki Disease 75 0.037
723
P MLR004 Malaria 74 0.037
724
CHR012 Chronic Granulomatous Disease 74 0.037
725
LSH001 Leishmaniasis 73 0.037
726
LKC001 Leukocyte Adhesion Deficiency 69 0.037
727
P MTB001 Metabolic Syndrome X 69 0.037
728
P MLG068 Malignant Glioma 68 0.037
729
P LVR013 Liver Disease 68 0.037
730
THR016 Thrombophlebitis 68 0.037
731
NNS005 Non-Small Cell Lung Carcinoma 67 0.037
732
P BLD042 Bladder Carcinoma 67 0.037
733
GSG001 Gas Gangrene 67 0.037
734
CMM004 Common Variable Immunodeficiency 66 0.037
735
P THR015 Thrombophilia 66 0.037
736
P PRT013 Portal Hypertension 65 0.037
737
P ATY010 Atypical Hemolytic-Uremic Syndrome 65 0.037
738
P GRV001 Graves' Disease 64 0.037
739
P ALP009 Alopecia Areata 64 0.037
740
CRY003 Cryptosporidiosis 63 0.037
741
CLN045 Colonic Benign Neoplasm 63 0.037
742
P RBL001 Rubella 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 60 0.037
747
P CRT033 Corticobasal Degeneration 58 0.037
748
AMN001 Amenorrhea 58 0.037
749
c XRD019 Xeroderma Pigmentosum, Group C 58 0.037
750
KNN001 Kennedy's Disease 58 0.037
751
CLS007 Classic Kaposi Sarcoma 57 0.037
752
P MYC008 Myocarditis 57 0.037
753
INT054 Intraocular Lymphoma 57 0.037
754
SPN051 Spondylitis 57 0.037
755
P PLC011 Pilocytic Astrocytoma 56 0.037
756
ILT001 Ileitis 56 0.037
757
c XRD012 Xeroderma Pigmentosum, Group D 55 0.037
758
c LTR001 Lateral Sclerosis 55 0.037
759
c LPR012 Leopard Syndrome 1 55 0.037
760
MLN020 Melanoma, Malignant, Somatic 55 0.037
761
P HYP014 Hyperuricemia 55 0.037
762
VNS010 Venous Thromboembolism 54 0.037
763
P DWR001 Dwarfism 54 0.037
764
P SML034 Small Cell Neuroendocrine Carcinoma 54 0.037
765
c OPH004 Ophthalmoplegia 54 0.037
766
PTT004 Pituitary Apoplexy 53 0.037
767
PPL021 Papilledema 53 0.037
768
P INT072 Intestinal Pseudo-Obstruction 53 0.037
769
ACT008 Actinic Keratosis 53 0.037
770
PNM001 Pneumocystosis 52 0.037
771
INT075 Intracranial Hypertension 52 0.037
772
HNT002 Hantavirus Pulmonary Syndrome 52 0.037
773
c LYM025 Lymphedema 52 0.037
774
RSD004 Rosai-Dorfman Disease 52 0.037
775
c CNG027 Congenital Hemolytic Anemia 51 0.037
776
FRZ001 Frozen Shoulder 51 0.037
777
GNG005 Gangliocytoma 51 0.037
778
GST027 Gastric Lymphoma 50 0.037
779
OVR012 Ovarian Serous Cystadenocarcinoma 50 0.037
780
GNT031 Genitopatellar Syndrome 49 0.037
781
SGT001 Sagittal Sinus Thrombosis 49 0.037
782
LMB024 Limbic Encephalitis 48 0.037
783
TXC002 Toxic Encephalopathy 48 0.037
784
P PRM012 Primary Polycythemia 48 0.037
785
CHY006 Chylous Ascites 48 0.037
786
PDT021 Pediatric Osteosarcoma 48 0.037
787
PRN029 Parainfluenza Virus Type 3 48 0.037
788
PNV001 Panuveitis 48 0.037
789
CRY001 Cryptogenic Organizing Pneumonia 47 0.037
790
PRT038 Protein-Energy Malnutrition 47 0.037
791
PRG060 Pregnancy Loss 47 0.037
792
END021 Endomyocardial Fibrosis 46 0.037
793
SPL004 Splenic Marginal Zone Lymphoma 46 0.037
794
MNN009 Meningoencephalitis 46 0.037
795
MCP006 Mucoepidermoid Carcinoma 45 0.037
796
PNH001 Panhypopituitarism 45 0.037
797
FSC004 Fasciitis 45 0.037
798
MCR017 Macrocytic Anemia 45 0.037
799
MLN057 Melanoma of Soft Parts 44 0.037
800
c APH002 Aphasia 43 0.037
801
c CNG003 Congenital Dyserythropoietic Anemia 42 0.037
802
LYM105 Lymphoma, Follicular, Somatic 40 0.037
803
MNN002 Mononeuritis Multiplex 38 0.037
804
P SYS007 Systemic Capillary Leak Syndrome 38 0.037
805
PHH001 Phaeohyphomycosis 37 0.037
806
MSN004 Mesenchymal Cell Neoplasm 37 0.037
807
XLN009 X-Linked Spinal-Bulbar Muscle Atrophy 34 0.037
808
THY025 Thymus Cancer 34 0.037
809
PLY021 Polyradiculopathy 32 0.037
810
P HRD104 Hereditary Multiple Osteochondromas 32 0.037
811
P CRN035 Cranial Nerve Palsy 31 0.037
812
P FNC044 Fanconi Anemia, Complementation Group C 31 0.037
813
DNG004 Dengue Fever, Protection Against 30 0.037
814
LNG004 Langerhans Cell Sarcoma 29 0.037
815
THP001 Thiopurine S Methyltranferase Deficiency 29 0.037
816
IMM001 Immune-Complex Glomerulonephritis 27 0.037
817
TRN028 Transient Acantholytic Dermatosis 25 0.037
818
DSC004 Discitis 25 0.037
819
ORB012 Orbital Cancer 24 0.037
820
MYL049 Myelofibrosis, Somatic 23 0.037
821
VRS001 Virus Associated Hemophagocytic Syndrome 21 0.037
822
DMD001 Demodicidosis 20 0.037
823
HRD137 Hereditary Isolated Aplastic Anemia 20 0.037
824
PRK066 Parkinsonism with Spasticity, X-Linked 20 0.037
825
MLT034 Multicystic Renal Dysplasia, Bilateral 18 0.037
826
RDT006 Radiation Induced Meningioma 18 0.037
827
P TYP008 Type 1 Diabetes Mellitus 95 0.033
828
PHN003 Phenylketonuria 83 0.033
829
FCT007 Factor Vii Deficiency 80 0.033
830
P WSK001 Wiskott-Aldrich Syndrome 79 0.033
831
CLD001 Cleidocranial Dysplasia 79 0.033
832
P OST002 Osteoporosis 76 0.033
833
CHD001 Chediak-Higashi Syndrome 76 0.033
834
c OST001 Osteopetrosis 75 0.033
835
P ALP006 Alpha Thalassemia 74 0.033
836
PRT036 Peritonitis 71 0.033
837
DBT011 Diabetic Retinopathy 70 0.033
838
P CNG401 Congenital Heart Disease 69 0.033
839
CHR003 Cherubism 68 0.033
840
P RCK004 Rickets 67 0.033
841
ALP001 Alopecia Universalis 67 0.033
842
MLB002 Male Breast Cancer 67 0.033
843
PRP027 Peripheral Vascular Disease 67 0.033
844
PLS006 Plasmodium Vivax Malaria 66 0.033
845
GST023 Gastric Ulcer 66 0.033
846
P BRN019 Bernard-Soulier Syndrome 64 0.033
847
PMS001 Poems Syndrome 64 0.033
848
P HRD057 Hereditary Pancreatitis 64 0.033
849
LBR002 Leber Hereditary Optic Neuropathy 64 0.033
850
c MCP010 Mucopolysaccharidosis 63 0.033
851
RBR001 Roberts Syndrome 63 0.033
852
P ESP024 Esophagitis 63 0.033
853
P KRT004 Keratitis 63 0.033
854
c INT070 Intestinal Obstruction 62 0.033
855
c THN001 Thanatophoric Dysplasia 61 0.033
856
TST014 Testicular Cancer 61 0.033
857
P CRV035 Cervical Cancer 60 0.033
858
CHR074 Choriocarcinoma 60 0.033
859
CNG402 Congenital Insensitivity to Pain with Anhidrosis 60 0.033
860
ASP003 Aseptic Meningitis 60 0.033
861
INT051 Intussusception 60 0.033
862
GLS001 Gliosarcoma 60 0.033
863
VSC003 Visceral Leishmaniasis 60 0.033
864
P PRM054 Primary Sclerosing Cholangitis 60 0.033
865
SPN020 Spondylosis 59 0.033
866
DBL002 Double Outlet Right Ventricle 59 0.033
867
EXF001 Exfoliation Syndrome 59 0.033
868
c GLY013 Glycogen Storage Disease 59 0.033
869
MLT001 Multiple Chemical Sensitivity 59 0.033
870
ANR004 Anuria 58 0.033
871
TBR011 Tuberculous Meningitis 58 0.033
872
SCN006 Secondary Syphilis 56 0.033
873
INS008 Insulin-Like Growth Factor I Deficiency 56 0.033
874
TTH006 Tooth Disease 55 0.033
875
STV001 Stevens-Johnson Syndrome 55 0.033
876
ACR005 Acrodermatitis 55 0.033
877
LMB002 Lambert-Eaton Myasthenic Syndrome 54 0.033
878
P CHR019 Choroid Plexus Carcinoma 54 0.033
879
MYL001 Myelitis 54 0.033
880
CYC004 Cyclic Hematopoiesis 54 0.033
881
PRT018 Portal Vein Thrombosis 54 0.033
882
APP001 Apparent Mineralocorticoid Excess Syndrome 53 0.033
883
c ANT034 Anterior Uveitis 53 0.033
884
c DFF019 Diffuse Gastric Cancer 53 0.033
885
PLM012 Pulmonary Sarcoidosis 53 0.033
886
P PRN022 Perineurioma 53 0.033
887
NM001 Noma 52 0.033
888
EMP001 Empty Sella Syndrome 51 0.033
889
GNG012 Gingival Overgrowth 51 0.033
890
c DRR001 Diarrhea 51 0.033
891
P CYS018 Cystitis 51 0.033
892
ERY003 Erythema Multiforme 51 0.033
893
P BRY001 Berylliosis 50 0.033
894
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 50 0.033
895
MLG121 Male Germ Cell Tumor, Somatic 50 0.033
896
STM007 Stomatitis 50 0.033
897
P PLG001 Pelger-Huet Anomaly 50 0.033
898
ASB001 Asbestosis 50 0.033
899
c ERY013 Erythrocytosis 50 0.033
900
SPN032 Spindle Cell Carcinoma 49 0.033
901
GST014 Gastrointestinal Lymphoma 49 0.033
902
CWP001 Cowpox 49 0.033
903
CRB090 Cerebral Hypoxia 49 0.033
904
NPH003 Nephrocalcinosis 48 0.033
905
BLT006 Bilateral Breast Cancer 47 0.033
906
DFF024 Diffuse Panbronchiolitis 46 0.033
907
LYM052 Lymphomatoid Papulosis 46 0.033
908
GNG008 Ganglioneuroblastoma 46 0.033
909
DRM011 Dermatophytosis 46 0.033
910
CNT025 Central Pontine Myelinolysis 46 0.033
911
ACT167 Acute Generalized Exanthematous Pustulosis 45 0.033
912
BLD101 Bladder Cancer Susceptibility 45 0.033
913
FML055 Familial Cylindromatosis 44 0.033
914
FST010 Fasting Hypoglycemia 44 0.033
915
BRS069 Breast Cancer, Somatic 44 0.033
916
CHR276 Chronic Active Epstein-Barr Virus Infection 43 0.033
917
NCR007 Necrotizing Fasciitis 43 0.033
918
SNL007 Senile Cataract 42 0.033
919
GND001 Gonadoblastoma 42 0.033
920
NPH017 Nephrosis 42 0.033
921
P DCR003 Dacryoadenitis 42 0.033
922
5FL001 5-Fluorouracil Toxicity 41 0.033
923
FBR002 Fibrosarcoma of Bone 41 0.033
924
c CHR208 Chromosome 17p Deletion 41 0.033
925
PRM014 Periampullary Adenocarcinoma 40 0.033
926
CRB085 Cerebral Hemorrhage 40 0.033
927
c CHR253 Chromosome 5q Deletion 39 0.033
928
ERY045 Erythrocytosis, Somatic 38 0.033
929
P OTT001 Otitis Externa 38 0.033
930
SBC024 Subcutaneous Panniculitis-Like T-Cell Lymphoma 38 0.033
931
BNZ002 Benzene Toxicity 37 0.033
932
DST056 Distal 22q11.2 Microdeletion Syndrome 37 0.033
933
ANM001 Anemia of Prematurity 36 0.033
934
TLS001 Tolosa-Hunt Syndrome 36 0.033
935
MCR213 Macroglobulinemia, Waldenstrom, Somatic 35 0.033
936
GRN009 Granulomatous Hepatitis 35 0.033
937
ABL001 Ablepharon Macrostomia Syndrome 35 0.033
938
BRC011 Brachial Plexus Neuropathy 34 0.033
939
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 34 0.033
940
PLM074 Pulmonary Function 34 0.033
941
P INF069 Infantile Neuroaxonal Dystrophy 1 33 0.033
942
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 33 0.033
943
EPD018 Epididymo-Orchitis 31 0.033
944
c CNG023 Congenital Fibrosarcoma 30 0.033
945
CRN061 Corneal Dystrophy Avellino Type 30 0.033
946
c ATS021 Autosomal Recessive Juvenile Parkinson Disease 30 0.033
947
c ATX026 Ataxia-Telangiectasia Variant 28 0.033
948
PRR008 Periarteritis Nodosa 28 0.033
949
c PRD013 Periodic Fever, Familial, Autosomal Dominant 25 0.033
950
BLN009 Balanoposthitis 25 0.033
951
PL2001 Pla2g6-Associated Neurodegeneration 24 0.033
952
CRT009 Critical Illness Polyneuropathy 24 0.033
953
c RNG024 Ring Chromosome 8 24 0.033
954
c MLG036 Malignant Spiradenoma 23 0.033
955
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 23 0.033
956
P BKV001 Bk-Virus Nephropathy 22 0.033
957
CHR463 Chronic Actinic Dermatitis 22 0.033
958
IND005 Indolent B Cell Lymphoma 21 0.033
959
EXT039 Extrapontine Myelinolysis 21 0.033
960
CD3004 Cd3epsilon Deficiency 19 0.033
961
MRC006 Mercaptopurine Toxicity 9 0.033
962
c TYP009 Type 2 Diabetes Mellitus 100 0.030
963
CYS001 Cystic Fibrosis 96 0.030
964
P FML011 Familial Adenomatous Polyposis 89 0.030
965
P AST005 Asthma 87 0.030
966
CDS001 Cadasil 84 0.030
967
WLS001 Wilson Disease 82 0.030
968
VNH001 Von Hippel-Lindau Disease 81 0.030
969
ACH004 Achondroplasia 79 0.030
970
P LPR003 Leprosy 77 0.030
971
CYS013 Cystinuria 76 0.030
972
P ALX003 Alexander Disease 76 0.030
973
P CLC005 Celiac Disease 74 0.030
974
P MLT042 Multiple Endocrine Neoplasia Type 2a 72 0.030
975
RLP001 Relapsing Polychondritis 72 0.030
976
WRN001 Werner Syndrome 71 0.030
977
CCC001 Coccidioidomycosis 71 0.030
978
GNT003 Genital Herpes 69 0.030
979
BLL006 Bullous Pemphigoid 69 0.030
980
PLY017 Polyarteritis Nodosa 69 0.030
981
CRY005 Cryptococcosis 67 0.030
982
TRG002 Trigeminal Neuralgia 67 0.030
983
DBT001 Diabetic Ketoacidosis 67 0.030
984
ALS001 Alstrom Syndrome 67 0.030
985
P TRN020 Turner Syndrome 67 0.030
986
PBL001 Piebaldism 66 0.030
987
P VLC001 Velocardiofacial Syndrome 66 0.030
988
OMN001 Omenn Syndrome 66 0.030
989
P GST044 Gastritis 65 0.030
990
DBN001 Dubin-Johnson Syndrome 65 0.030
991
c TXP001 Toxoplasmosis 65 0.030
992
STR067 Stroke, Ischemic 64 0.030
993
P RHN004 Rhinitis 64 0.030
994
ALP007 Alpha 1-Antitrypsin Deficiency 64 0.030
995
c LNG028 Long Qt Syndrome 64 0.030
996
PRT014 Protein S Deficiency 64 0.030
997
MXD005 Mixed Connective Tissue Disease 64 0.030
998
TTN003 Tetanus 64 0.030
999
KRN002 Kearns-Sayre Syndrome 63 0.030
1000
BRR003 Barrett's Esophagus 63 0.030
1001
P ERY008 Erythromelalgia 63 0.030
1002
ISC004 Ischemia 62 0.030
1003
PRL009 Prolactinoma 62 0.030
1004
LYM009 Lymphocytic Choriomeningitis 62 0.030
1005
GLD001 Goldenhar Syndrome 62 0.030
1006
CRN036 Craniopharyngioma 62 0.030
1007
ACR008 Acrocallosal Syndrome 61 0.030
1008
CDL003 Caudal Regression Syndrome 61 0.030
1009
c CHR023 Charcot-Marie-Tooth Disease Type 2 61 0.030
1010
c LMB006 Limb-Girdle Muscular Dystrophy 61 0.030
1011
c ANG015 Angioedema 60 0.030
1012
MCS003 Mucous Membrane Pemphigoid 60 0.030
1013
BRC012 Brucellosis 60 0.030
1014
ACR003 Acrodermatitis Enteropathica 59 0.030
1015
P BRN009 Burning Mouth Syndrome 59 0.030
1016
P PRC019 Precocious Puberty 59 0.030
1017
c LRY016 Laryngeal Carcinoma 59 0.030
1018
P SYN007 Synovitis 59 0.030
1019
SLD003 Sialadenitis 59 0.030
1020
c HPT003 Hepatitis a 58 0.030
1021
ICH002 Ichthyosis Bullosa of Siemens 58 0.030
1022
c CNG124 Congenital Rubella 58 0.030
1023
LPD010 Lipodystrophy 58 0.030
1024
TMP001 Temporal Lobe Epilepsy 58 0.030
1025
c BRG001 Brugada Syndrome 58 0.030
1026
CNN005 Connective Tissue Disease 58 0.030
1027
HDC001 Headache 57 0.030
1028
P WVR001 Weaver Syndrome 57 0.030
1029
FLR002 Filariasis 57 0.030
1030
ACN011 Acne 57 0.030
1031
NDL013 Nodular Regenerative Hyperplasia 57 0.030
1032
P MYM002 Moyamoya Disease 57 0.030
1033
INT146 Intervertebral Disc Disease 57 0.030
1034
P GNT008 Giant Cell Tumor 57 0.030
1035
c CTR002 Cataract 57 0.030
1036
ANH002 Anhidrosis 57 0.030
1037
P HYP024 Hypoparathyroidism 57 0.030
1038
ETN001 Eating Disorder 56 0.030
1039
PRT019 Protein-Losing Enteropathy 55 0.030
1040
ACN001 Acinar Cell Carcinoma 55 0.030
1041
P SJG002 Sjogren-Larsson Syndrome 54 0.030
1042
BRN004 Brain Edema 54 0.030
1043
DSM007 Desmoplastic Small Round Cell Tumor 54 0.030
1044
NPH011 Nephroblastoma 54 0.030
1045
P INT064 Intermediate Uveitis 54 0.030
1046
DBT006 Diabetic Macular Edema 54 0.030
1047
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 54 0.030
1048
P HYP141 Hyperphenylalaninemia 54 0.030
1049
PTT037 Pituitary Tumors 53 0.030
1050
ATY008 Atypical Lipomatous Tumor 53 0.030
1051
IGG001 Iga Glomerulonephritis 53 0.030
1052
c PST022 Posterior Uveal Melanoma 53 0.030
1053
TNG003 Tongue Cancer 53 0.030
1054
GST045 Gastroenteritis 53 0.030
1055
P PRK001 Porokeratosis 52 0.030
1056
LPS007 Lupus Nephritis 52 0.030
1057
c TLN008 Telangiectasia, Hereditary Hemorrhagic, Type 5 52 0.030
1058
PRP002 Periapical Granuloma 52 0.030
1059
MMB002 Membranous Glomerulonephritis 52 0.030
1060
c HPT007 Hepatitis E 52 0.030
1061
JNT002 Joint Disorders 52 0.030
1062
GLS007 Glossitis 51 0.030
1063
HMR002 Hemarthrosis 51 0.030
1064
JVN033 Juvenile Nasopharyngeal Angiofibroma 51 0.030
1065
c FML024 Familial Melanoma 51 0.030
1066
ADN014 Adenomatoid Tumor 51 0.030
1067
MLL001 Molluscum Contagiosum 51 0.030
1068
LPD004 Lipoid Nephrosis 50 0.030
1069
WBR001 Weber Syndrome 50 0.030
1070
c KRT005 Keratoacanthoma 50 0.030
1071
P CST002 Castleman's Disease 50 0.030
1072
RHB017 Rhabdoid Tumor 50 0.030
1073
FBR009 Fibrous Dysplasia 50 0.030
1074
MMR004 Memory Impairment 50 0.030
1075
BRN018 Borna Disease 50 0.030
1076
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 50 0.030
1077
FCT005 Factor Xiii Deficiency 50 0.030
1078
ANL011 Anal Canal Carcinoma 50 0.030
1079
CHR288 Chronic Recurrent Multifocal Osteomyelitis 50 0.030
1080
c ATM024 Autoimmune Pancreatitis 50 0.030
1081
OPT009 Optic Neuritis 49 0.030
1082
INF058 Inflammatory Myofibroblastic Tumor 49 0.030
1083
PYG006 Pyogenic Granuloma 49 0.030
1084
CRY021 Cryoglobulinemic Vasculitis 49 0.030
1085
NRT004 Neuritis 49 0.030
1086
SMN007 Seminoma 49 0.030
1087
MDT001 Mediterranean Spotted Fever 48 0.030
1088
RTN003 Retinal Ischemia 48 0.030
1089
CNV002 Conversion Disorder 48 0.030
1090
TRC040 Tracheoesophageal Fistula 48 0.030
1091
GMM002 Gamma Chain Deficiency 48 0.030
1092
IMM030 Immunodeficiency, Common Variable, 3 48 0.030
1093
ESN006 Eosinophilic Meningitis 47 0.030
1094
VTM002 Vitamin B12 Deficiency 47 0.030
1095
MCR037 Macroglossia 47 0.030
1096
ADR021 Adrenocorticotropic Hormone Deficiency 46 0.030
1097
URT010 Ureteral Obstruction 46 0.030
1098
MTG002 Mutagen Sensitivity 46 0.030
1099
c ATM019 Autoimmune Polyendocrine Syndrome 46 0.030
1100
P ART084 Arteriovenous Fistula 46 0.030
1101
PLS009 Plasma Cell Neoplasm 46 0.030
1102
PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 46 0.030
1103
TNS001 Tenosynovial Giant Cell Tumor 46 0.030
1104
CHR404 Chronic Granulomatous Disease Due to Deficiency of Ncf-1 46 0.030
1105
P CRB088 Cerebral Atrophy 46 0.030
1106
c CHR048 Chronic Rhinitis 46 0.030
1107
P BRS044 Breast Adenocarcinoma 46 0.030
1108
c RCR022 Recurrent Acute Pancreatitis 46 0.030
1109
MXL004 Maxillary Sinus Squamous Cell Carcinoma 46 0.030
1110
STC004 Stachybotrys Chartarum 45 0.030
1111
DHY007 Dihydropteridine Reductase Deficiency 45 0.030
1112
EPL002 Epilepsy Syndrome 45 0.030
1113
RPD002 Rapadilino Syndrome 45 0.030
1114
BWN003 Bowenoid Papulosis 45 0.030
1115
INT067 Interstitial Nephritis 45 0.030
1116
P NRL007 Neurologic Diseases 45 0.030
1117
INF034 Infective Endocarditis 44 0.030
1118
P IRD010 Iridogoniodysgenesis Syndrome 44 0.030
1119
SPR005 Superficial Basal Cell Carcinoma 44 0.030
1120
c TRC005 Tracheal Stenosis 44 0.030
1121
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 44 0.030
1122
QDR001 Quadriplegia 43 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 42 0.030
1127
THY043 Thymic Hyperplasia 42 0.030
1128
TRT001 Teratocarcinoma 42 0.030
1129
EST005 Esotropia 42 0.030
1130
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 42 0.030
1131
c BRS076 Breast Cancer, Early-Onset 42 0.030
1132
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 42 0.030
1133
INT071 Intestinal Perforation 42 0.030
1134
CRB132 Cerebral Sinovenous Thrombosis 42 0.030
1135
PRV003 Perivascular Epithelioid Cell Tumor 42 0.030
1136
PLN006 Poland Syndrome 41 0.030
1137
c ACQ012 Acquired Angioedema 41 0.030
1138
BRS079 Breast Cancer, Protection Against 41 0.030
1139
GST071 Gastrointestinal Carcinoma 41 0.030
1140
MNN034 Mannose-Binding Lectin Deficiency 41 0.030
1141
P MSC109 Mosaic Variegated Aneuploidy Syndrome 1 40 0.030
1142
WRN003 Wernicke Encephalopathy 40 0.030
1143
EPD053 Epidermal Nevus, Somatic 40 0.030
1144
INP001 Inappropriate Adh Syndrome 40 0.030
1145
GNG006 Gingival Hypertrophy 39 0.030
1146
PLY013 Polymyalgia Rheumatica 39 0.030
1147
ENT007 Enteropathica 39 0.030
1148
P HYP071 Hypersensitivity Reaction Type Ii Disease 39 0.030
1149
PTY004 Pityriasis Lichenoides 39 0.030
1150
MLG065 Malignant Fibroxanthoma 39 0.030
1151
c HVY001 Heavy Chain Disease 39 0.030
1152
GST012 Gastroesophageal Junction Adenocarcinoma 38 0.030
1153
c MLR021 Malaria, Severe 38 0.030
1154
GST020 Gastric Antral Vascular Ectasia 38 0.030
1155
CHL056 Cheilitis 38 0.030
1156
CMB021 Combined Pituitary Hormone Deficiency 38 0.030
1157
IRD001 Iridocyclitis 38 0.030
1158
PTT021 Pituitary Hormone Deficiency, Combined 2 37 0.030
1159
ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 37 0.030
1160
P GMM003 Gamma Heavy Chain Disease 37 0.030
1161
SZR001 Sezary's Disease 37 0.030
1162
P RNG004 Ring Chromosome 1 37 0.030
1163
FTD001 Foot Drop 36 0.030
1164
GTT002 Guttate Psoriasis 36 0.030
1165
TST004 Testicular Lymphoma 36 0.030
1166
KLD001 Keloids 36 0.030
1167
c JVN009 Juvenile Pilocytic Astrocytoma 36 0.030
1168
OPT006 Optic Nerve Disease 35 0.030
1169
ATY005 Atypical Teratoid Rhabdoid Tumor 35 0.030
1170
CHR415 Chronic Venous Leg Ulcers 35 0.030
1171
SPP002 Sipple Syndrome 35 0.030
1172
BLD087 Bladder Cancer, Somatic 35 0.030
1173
DYS012 Dyshidrosis 34 0.030
1174
P LNG038 Lung Small Cell Carcinoma 34 0.030
1175
NCR009 Necrobiotic Xanthogranuloma 34 0.030
1176
NVS013 Nevus Sebaceous, Somatic 34 0.030
1177
c ACQ010 Acquired Polycythemia 34 0.030
1178
HPT063 Hepatitis B Virus Infection 33 0.030
1179
ENG004 Engraftment Syndrome 32 0.030
1180
c RHB009 Rhabdomyosarcoma 2, Alveolar 32 0.030
1181
CRV036 Cervical Carcinosarcoma 32 0.030
1182
CNG058 Congenital Antithrombin Deficiency Type 3 32 0.030
1183
P SVR013 Severe Congenital Neutropenia Autosomal Recessive 3 32 0.030
1184
TRC006 Trichosporonosis 32 0.030
1185
CHL040 Cholangiolocellular Carcinoma 32 0.030
1186
BRG002 Berger Disease 31 0.030
1187
RMS005 Ramsay-Hunt Syndrome 31 0.030
1188
TST021 Testicular Germ Cell Tumor 31 0.030
1189
c CHR091 Chronic Meningitis 30 0.030
1190
c RNG022 Ring Chromosome 6 29 0.030