Search results for "leukemia"

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

3436 hits were found for 'leukemia'

# Family MCID Name MIFTS Score
1
c LKM062 Leukemia, Acute Lymphoblastic 63 8.052
2
c CHR090 Chronic Lymphocytic Leukemia 73 7.049
3
P MYL006 Myeloid Leukemia 67 7.004
4
P LKM002 Leukemia 70 6.957
5
c LKM061 Leukemia, Acute Myeloid 71 6.850
6
P LKM068 Leukemia, Chronic Myeloid, Somatic 65 6.197
7
LKM067 Leukemia, Acute Promyelocytic, Somatic 55 5.365
8
MGK001 Megakaryocytic Leukemia 53 4.874
9
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 62 4.759
10
c ACT073 Acute Leukemia 61 4.518
11
ACT216 Acute Leukemia of Ambiguous Lineage 30 4.271
12
P LYM026 Lymphoblastic Leukemia 60 4.157
13
c ADL017 Adult T-Cell Leukemia 59 4.106
14
NTR003 Natural Killer Cell Leukemia 46 3.772
15
P ACT074 Acute Lymphocytic Leukemia 54 3.678
16
c LKM060 Leukemia, Acute Lymphoblastic 3 49 3.654
17
c CHR285 Chronic Myelomonocytic Leukemia 54 3.610
18
ACT200 Acute Monoblastic Leukemia 44 3.512
19
HRY003 Hairy Cell Leukemia 56 3.426
20
P TCL004 T-Cell Leukemia 44 3.418
21
c CHR418 Chronic Leukemia 48 3.409
22
c ACT020 Acute T Cell Leukemia 38 3.396
23
P ACT117 Acute Myelomonocytic Leukemia 46 3.367
24
c ADL052 Adult Acute Lymphocytic Leukemia 41 3.252
25
P MNC007 Monocytic Leukemia 52 3.208
26
ACT098 Acute Erythroid Leukemia 34 3.136
27
c CHR064 Chronic Monocytic Leukemia 42 3.023
28
ACT103 Acute Lymphoblastic Leukemia, Childhood 22 2.971
29
ACT113 Acute Myeloblastic Leukemia with Maturation 40 2.947
30
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 17 2.928
31
c ACT009 Acute Monocytic Leukemia 46 2.869
32
PLS016 Plasma Cell Leukemia 52 2.867
33
CHL061 Childhood Leukemia 47 2.852
34
PRL017 Prolymphocytic Leukemia 44 2.835
35
TCL002 T-Cell Large Granular Lymphocyte Leukemia 41 2.825
36
MST002 Mast-Cell Leukemia 50 2.809
37
c TCL005 T-Cell Prolymphocytic Leukemia 52 2.796
38
c SBC004 Subacute Myeloid Leukemia 34 2.751
39
LRG008 Large Granular Lymphocyte Leukemia 39 2.739
40
LYM067 Lymphoid Leukemia 38 2.728
41
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 2.717
42
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 19 2.679
43
c LKM005 Leukemia, T-Cell, Chronic 21 2.660
44
NNN022 Noonan Syndrome-Like Disorder with or Without Juvenile Myelomonocytic Leukemia 30 2.649
45
CNT018 Central Nervous System Leukemia 38 2.548
46
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 24 2.510
47
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 13 2.442
48
HCL001 Hcl-V 33 2.425
49
ACT118 Acute Non Lymphoblastic Leukemia 27 2.413
50
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 27 2.403
51
c LKM004 Leukemia, B-Cell, Chronic 24 2.403
52
c LKM055 Leukemia, Acute Lymphoblastic 2 21 2.396
53
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 39 2.395
54
CHR286 Chronic Neutrophilic Leukemia 44 2.382
55
c LKM056 Leukemia, Chronic Lymphocytic 2 40 2.376
56
c LKM050 Leukemia, Chronic Lymphocytic 1 21 2.357
57
P BCL005 B Cell Prolymphocytic Leukemia 44 2.347
58
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 32 2.344
59
PLS003 Plasmacytic Leukemia 22 2.281
60
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 33 2.261
61
c LKM051 Leukemia, Chronic Lymphocytic 3 21 2.261
62
SBL003 Subleukemic Leukemia 11 2.202
63
NLL001 Null-Cell Leukemia 29 2.180
64
P CHR562 Chronic Myelocytic Leukemia 39 2.099
65
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 31 2.098
66
CRB138 Core Binding Factor Acute Myeloid Leukemia 41 2.036
67
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 20 2.027
68
ACT095 Acute Biphenotypic Leukemia 33 2.027
69
ALK003 Aleukemic Leukemia Cutis 32 1.998
70
RFR002 Refractory Hairy Cell Leukemia 31 1.983
71
TST003 Testicular Leukemia 32 1.983
72
NNT007 Neonatal Leukemia 34 1.941
73
ERY051 Erythroleukemia, Familial 23 1.939
74
c ACT219 Acute Myeloid Leukemia, Flt3-Related 32 1.930
75
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 23 1.930
76
ACT222 Acute Pre-B-Cell Lymphoblastic Leukemia 21 1.921
77
MYL055 Myeloid/lymphoid or Mixed Lineage Leukemia 29 1.911
78
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 31 1.896
79
ALK002 Aleukemic Monocytic Leukemia Cutis 10 1.896
80
SPL013 Splenic Manifestation of Leukemia 14 1.885
81
CBP001 Cebpa-Associated Familial Acute Myeloid Leukemia 5 1.877
82
CLL014 Cll/sll 42 1.819
83
CHR563 Chronic Eosinophilic Leukemia 46 1.772
84
LYM040 Lymphoblastic Lymphoma 51 1.720
85
BND002 B- and T-Cell Mixed Leukemia 18 1.632
86
PDT026 Pediatric T-Cell Leukemia 13 1.623
87
AML051 Aml with Myelodysplasia-Related Features 18 1.601
88
ACT224 Acute Promyelocytic Leukemia Pml/rara Type 12 1.597
89
P 8P1002 8p11 Myeloproliferative Syndrome 37 1.587
90
P LFR001 Li-Fraumeni Syndrome 79 1.582
91
ACT196 Acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2) 13 1.571
92
c SBC006 Subacute Leukemia 11 1.571
93
c HMN021 Human T-Cell Leukemia Virus Type 1 51 1.556
94
c INH015 Inherited Acute Myeloid Leukemia 25 1.555
95
c SBC015 Subacute Monocytic Leukemia 12 1.555
96
FML045 Familial Mosaic Monosomy 7 Syndrome 7 1.539
97
CHL029 Childhood Precursor T-Lymphoblastic Lymphoma/leukemia 12 1.534
98
ACT223 Acute Promyelocytic Leukemia Numa/rara Type 4 1.534
99
PST004 Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 7 1.529
100
PRG005 Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 7 1.529
101
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 16 1.416
102
c ADL093 Adult Acute Monocytic Leukemia 16 1.368
103
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 16 1.331
104
ACT177 Acute Basophilic Leukemia 34 1.286
105
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 14 1.246
106
c HMN022 Human T-Cell Leukemia Virus Type 2 45 1.227
107
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 13 1.196
108
NSY001 N Syndrome 42 1.192
109
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 24 1.183
110
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 13 1.177
111
ACT217 Acute Myeloid Leukemia with Recurrent Genetic Anomaly 11 1.167
112
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 15 1.153
113
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 22 1.148
114
c HMN023 Human T-Cell Leukemia Virus Type 3 15 1.137
115
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 14 1.137
116
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 45 1.134
117
c ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 29 1.131
118
c ACT198 Acute Myeloid Leukemia with T(6;9)(p23;q34) 17 1.131
119
ALK014 Aleukemic Mast Cell Leukemia 11 1.131
120
HRY001 Hairy Cell Leukemia of Spleen 17 1.124
121
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 24 1.121
122
P ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 16 1.121
123
EMB016 Emberger Syndrome 29 1.117
124
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 13 1.117
125
BLN016 Bilineal Acute Leukemia 9 1.117
126
PRC009 Precursor T-Lymphoblastic Lymphoma/leukemia Refractory 10 1.117
127
DFN299 Deafness-Lymphedema-Leukemia Syndrome 9 1.113
128
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 9 1.109
129
c MYL018 Myelocytic Leukemia-Like Syndrome, Familial, Chronic 4 1.105
130
UNC013 Unclassified Acute Myeloid Leukemia 6 1.100
131
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 13 1.094
132
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 8 1.094
133
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 8 1.094
134
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 12 1.094
135
SPL002 Splenic Manifestation of Prolymphocytic Leukemia 5 1.094
136
SPL010 Splenic Manifestation of Hairy Cell Leukemia 10 1.094
137
CLS019 Classic Mast Cell Leukemia 5 1.094
138
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 2 1.094
139
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 9 1.088
140
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 4 1.088
141
c ACT220 Acute Myeloid Leukemia, Kit-Related 7 1.088
142
c ACT221 Acute Myeloid Leukemia, Somatic Dnmt3a-Related 6 1.088
143
c NPM001 Npm1-Related Acute Myeloid Leukemia 7 1.088
144
WTL002 Wt Limb-Blood Syndrome 19 1.081
145
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 16 1.081
146
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 8 1.072
147
P LYM118 Lymphoma 68 0.508
148
BNM001 Bone Marrow Cancer 56 0.401
149
LYM024 Lymphatic System Disease 49 0.394
150
LYM023 Lymphatic System Cancer 35 0.391
151
SPN041 Spinal Cord Disease 50 0.387
152
MYL009 Myelodysplastic Syndrome 73 0.353
153
c HYP073 Hypersensitivity Reaction Type Iv Disease 45 0.343
154
BNC003 Bone Cancer 44 0.339
155
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 36 0.332
156
IMM127 Immune System Cancer 41 0.330
157
c ADL001 Adult Lymphoma 40 0.303
158
LYM019 Lymphosarcoma 52 0.290
159
c CHR092 Chronic Myeloproliferative Disease 50 0.287
160
TNP003 Tn Polyagglutination Syndrome, Somatic 30 0.279
161
HMT018 Hematopoietic Stem Cell Transplantation 39 0.279
162
HMT002 Hematologic Cancer 62 0.275
163
P BCL006 B-Cell Lymphomas 64 0.253
164
INC022 Inclusion-Cell Disease 46 0.238
165
c PRM023 Pre-Malignant Neoplasm 42 0.235
166
RFR004 Refractory Hematologic Cancer 27 0.226
167
BNL002 Bone Lymphoma 34 0.223
168
PRP021 Peripheral Nervous System Neoplasm 49 0.213
169
BNS002 Bone Structure Disease 37 0.210
170
ADL002 Adult Syndrome 53 0.206
171
ACR041 Acromelic Frontonasal Dysostosis 45 0.201
172
BRT030 Birth Defects 44 0.201
173
OCL009 Ocular Cancer 61 0.191
174
PRM151 Primary Bone Lymphoma 26 0.190
175
PLV005 Pelviureteric Junction Obstruction 43 0.189
176
MYL004 Myelodysplastic Myeloproliferative Cancer 46 0.183
177
LYM115 Lymphoma, Non-Hodgkin 64 0.179
178
P MYL007 Myeloma 52 0.179
179
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.176
180
P CHR084 Chromosomal Disease 37 0.175
181
P NRV006 Nervous System Cancer 62 0.174
182
ACD009 Acid-Labile Subunit, Deficiency of 37 0.172
183
C3D001 C3 Deficiency 50 0.168
184
SRC014 Sarcoma 66 0.161
185
c MLT019 Multiple Myeloma 77 0.161
186
ATN003 Autonomic Nervous System Neoplasm 43 0.157
187
LKC003 Leukocyte Disease 45 0.157
188
SNS023 Sensory System Cancer 45 0.153
189
RFR010 Refractory Anemia 43 0.151
190
BND014 Bone Development Disease 40 0.150
191
P CNT005 Central Nervous System Lymphoma 51 0.150
192
ACR002 Acrocapitofemoral Dysplasia 35 0.149
193
P ACT135 Acute Graft Versus Host Disease 52 0.148
194
PLS009 Plasma Cell Neoplasm 47 0.147
195
BLD053 Blood Platelet Disease 44 0.147
196
FRB001 Farber Lipogranulomatosis 54 0.145
197
CHL071 Child Syndrome 58 0.143
198
c LYM106 Lymphoproliferative Syndrome 1 33 0.143
199
KDS001 Kid Syndrome 53 0.142
200
GST014 Gastrointestinal Lymphoma 31 0.142
201
c LYM107 Lymphoproliferative Syndrome 2 32 0.141
202
RPR002 Reproductive System Disease 45 0.139
203
P NTR004 Neutropenia 59 0.138
204
P MYL005 Myelofibrosis 67 0.137
205
PDT001 Pediatric Lymphoma 39 0.136
206
END072 Endotheliitis 41 0.135
207
GDS001 Good Syndrome 46 0.135
208
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.134
209
c CLL013 Cell Type Cancer 46 0.134
210
CSY001 C Syndrome 49 0.133
211
WLL006 Wells Syndrome 57 0.133
212
BRK010 Burkitt Lymphoma 66 0.131
213
DFC004 Deficiency Anemia 64 0.131
214
c CHR417 Chronic Graft Versus Host Disease 50 0.130
215
c PRM226 Primary Central Nervous System Lymphoma 51 0.130
216
DWN001 Down Syndrome 65 0.129
217
HDG012 Hodgkin Lymphoma 75 0.128
218
P ESN007 Eosinophilia 61 0.128
219
MNT001 Mantle Cell Lymphoma 72 0.127
220
BLD054 Blood Protein Disease 38 0.126
221
HRT007 Heart Cancer 51 0.125
222
P HRT017 Heart Tumor 34 0.125
223
P RFR008 Refractory Anemia with Excess Blasts 30 0.125
224
ALR002 Al-Raqad Syndrome 36 0.123
225
c ADL079 Adult Heart Tumor 17 0.120
226
ALN001 Aland Island Eye Disease 45 0.119
227
PRP036 Peripheral T-Cell Lymphoma 44 0.118
228
DFF005 Diffuse Large B-Cell Lymphoma 57 0.118
229
ORL011 Oral Cancer 53 0.117
230
HML018 Homologous Wasting Disease 14 0.117
231
P THR014 Thrombocytopenia 63 0.116
232
P HPT021 Hepatitis 74 0.116
233
P ORL007 Oral Cavity Cancer 58 0.114
234
P HML002 Hemolytic Anemia 60 0.113
235
P FLL037 Follicular Lymphoma 68 0.113
236
VND001 Vein Disease 51 0.113
237
P MST009 Mastocytosis 54 0.113
238
CNT010 Central Nervous System Hematologic Cancer 20 0.113
239
ARG006 Aregenerative Anemia 21 0.113
240
MYL003 Myeloid Sarcoma 48 0.112
241
ATN002 Autonomic Nervous System Disease 46 0.111
242
LYM127 Lymphatic Malformations 38 0.111
243
P APL001 Aplastic Anemia 74 0.109
244
P SPS003 Spastic Diplegia 49 0.108
245
MCR004 Macroglobulinemia 48 0.108
246
RTC009 Reticulum Cell Sarcoma 46 0.108
247
LYM126 Lymphoma Aids Related 17 0.107
248
P BRS047 Breast Cancer 100 0.106
249
GLC077 Glucocorticoid Therapy, Response to 17 0.105
250
RTC005 Reticulosarcoma 46 0.104
251
P HYP098 Hypereosinophilic Syndrome 48 0.103
252
P HYP004 Hypercalcemia 54 0.103
253
c ATM010 Autoimmune Hemolytic Anemia 59 0.103
254
RFR001 Refractory Plasma Cell Neoplasm 17 0.103
255
RFR007 Refractory Anemia with Excess Blasts in Transformation 21 0.102
256
c RFR015 Refractory Anemia with Excess Blasts Type 1 14 0.102
257
c RFR014 Refractory Anemia with Excess Blasts Type 2 17 0.102
258
RDT005 Radiation Induced Cancer 26 0.101
259
PCK002 Pick Disease 66 0.100
260
c SYS004 Systemic Mastocytosis 60 0.100
261
c FLL041 Follicular Lymphoma 1 45 0.100
262
P HST010 Histiocytosis 56 0.100
263
MXD023 Mixed Cell Type Cancer 45 0.100
264
GRN017 Granulocytopenia 39 0.098
265
ACT228 Acute Radiation Syndrome 20 0.097
266
P ESS003 Essential Thrombocythemia 66 0.096
267
P PLY018 Polycythemia 58 0.096
268
P PNM007 Pneumonia 67 0.095
269
VSC006 Vascular Cancer 51 0.095
270
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.095
271
P ART022 Arthritis 73 0.094
272
PRS047 Prostatitis 56 0.094
273
HRT003 Heart Lymphoma 31 0.094
274
MRG003 Marginal Zone B-Cell Lymphoma 50 0.094
275
HRT029 Heart Tumor of the Child 16 0.093
276
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.092
277
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 35 0.091
278
PRR002 Pure Red-Cell Aplasia 47 0.091
279
RCH001 Richter's Syndrome 45 0.091
280
P BLD051 Blood Coagulation Disease 44 0.091
281
P KDN017 Kidney Cancer 67 0.089
282
LPD004 Lipoid Nephrosis 49 0.089
283
VSC008 Vascular Hemostatic Disease 30 0.089
284
GLC037 Glucocorticoid Resistance 57 0.088
285
TCL019 T-Cell Childhood Lymphoblastic Lymphoma 14 0.088
286
BNM005 Bone Marrow Necrosis 30 0.088
287
P MNN013 Meningitis 66 0.087
288
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 40 0.087
289
P WLD002 Waldenstrom Macroglobulinemia 62 0.086
290
PRD011 Proud Syndrome 42 0.085
291
P ASP006 Aspergillosis 61 0.085
292
c CRN214 Coronary Heart Disease 5 22 0.085
293
PLS025 Plasmablastic Lymphoma 46 0.085
294
LYM012 Lymphoplasmacytic Lymphoma 46 0.084
295
P NRP001 Neuropathy 57 0.084
296
LKS001 Leukostasis 39 0.084
297
c BNG076 Benign Exophthalmos Syndrome 15 0.084
298
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.084
299
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 36 0.084
300
DSS009 Disseminated Intravascular Coagulation 52 0.083
301
P THY032 Thyroiditis 57 0.083
302
WLM007 Wilms Tumor Susceptibility-5 64 0.082
303
P NRF002 Neurofibromatosis 66 0.082
304
P INF038 Influenza 71 0.082
305
VSC011 Vasculitis 62 0.082
306
PRP019 Peripheral Nervous System Disease 52 0.081
307
BCT015 Bacteremia 50 0.081
308
SVR004 Severe Combined Immunodeficiency 71 0.080
309
SPL012 Splenic Disease 48 0.080
310
CRB009 Cerebritis 36 0.080
311
WTH001 Withdrawal Disorder 36 0.080
312
THR004 Thrombocytosis 55 0.079
313
SPL004 Splenic Marginal Zone Lymphoma 43 0.079
314
HPT074 Hepatic Adenoma, Somatic 35 0.078
315
TRP002 Tropical Spastic Paraparesis 55 0.078
316
SPL011 Spleen Cancer 38 0.078
317
SPS057 Spasticity 41 0.078
318
SPS019 Spastic Paraparesis 34 0.078
319
NNH003 Non-Hodgkin Lymphoma, Childhood 13 0.078
320
HPT023 Hepatocellular Carcinoma 90 0.077
321
P RHM011 Rheumatoid Arthritis 87 0.077
322
c CLD010 Cold-Induced Sweating Syndrome 1 43 0.077
323
P ANP001 Anaplastic Large Cell Lymphoma 58 0.077
324
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.077
325
P PNC001 Pancytopenia 53 0.077
326
HYP266 Hypoxia 55 0.077
327
RTN023 Retinitis 49 0.077
328
P ATX030 Ataxia-Telangiectasia 78 0.077
329
MLN008 Melanoma 61 0.077
330
c MLG054 Malignant Histiocytosis 55 0.077
331
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.076
332
P RTN024 Retinoblastoma 75 0.076
333
WST001 West Syndrome 61 0.076
334
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 30 0.076
335
P CRN178 Coronary Heart Disease 6 22 0.075
336
c MCR162 Macroglobulinemia, Waldenstrom 2 19 0.075
337
LYM048 Lymphoma, Large-Cell, Immunoblastic 19 0.075
338
P PNC044 Pancreatitis 62 0.074
339
c MCR161 Macroglobulinemia, Waldenstrom 1 28 0.074
340
PLS011 Plasmacytoma 57 0.074
341
c RTN162 Retinitis Pigmentosa 2 50 0.073
342
P CTN015 Cutaneous T Cell Lymphoma 41 0.073
343
SPL018 Splenomegaly 45 0.073
344
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.073
345
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.072
346
c SVR003 Severe Congenital Neutropenia 54 0.072
347
DPH001 Diphtheria 55 0.072
348
P ATX004 Ataxia 53 0.072
349
c CRN173 Coronary Heart Disease 8 19 0.072
350
SML025 Small Non-Cleaved Cell Lymphoma 21 0.072
351
P PRS040 Prostate Cancer 89 0.071
352
P LNG032 Lung Cancer 92 0.071
353
MYC006 Mycosis Fungoides 66 0.071
354
P DBT005 Diabetes Insipidus 53 0.071
355
UTR033 Uterine Corpus Cancer 50 0.071
356
MDS022 Mediastinitis 37 0.071
357
DSS003 Disseminated Eosinophilic Collagen Disease 17 0.071
358
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.070
359
MGK002 Megakaryocytic Tumor 32 0.070
360
P NRB001 Neuroblastoma 70 0.070
361
HDG004 Hodgkin's Granuloma 25 0.070
362
c PRM149 Primary Hypereosinophilic Syndrome 39 0.070
363
PRL032 Perlman Syndrome 55 0.069
364
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 59 0.069
365
GNG013 Gingivitis 61 0.069
366
PRP030 Purpura 60 0.069
367
LRN003 Learning Disability 49 0.069
368
HDG006 Hodgkin's Paragranuloma 18 0.069
369
PST046 Post-Transplant Lymphoproliferative Disease 53 0.069
370
TTR011 Tetraploidy 41 0.069
371
c CHR096 Chronic Pulmonary Heart Disease 40 0.069
372
GST019 Gastrointestinal Stromal Tumor 73 0.068
373
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.068
374
P ADN016 Adenocarcinoma 69 0.068
375
BRN028 Brain Cancer 69 0.067
376
MTH009 Mouth Disease 63 0.067
377
BNM011 Bone Marrow Failure Syndrome 2 29 0.067
378
HMG002 Hemoglobinuria 49 0.067
379
c CRN177 Coronary Heart Disease 7 21 0.067
380
ADJ001 Adjustment Disorder 38 0.067
381
P OBS005 Obesity 91 0.066
382
LNG024 Langerhans-Cell Histiocytosis 64 0.066
383
c TRC078 Trichohepatoenteric Syndrome 2 30 0.066
384
c CNT035 Central Nervous System Disease 60 0.066
385
HV1006 Hiv-1 80 0.065
386
TBR010 Tuberculosis 70 0.065
387
LKM001 Leukemoid Reaction 46 0.065
388
c INV001 Invasive Aspergillosis 44 0.065
389
RBR001 Roberts Syndrome 61 0.064
390
c HPT016 Hepatitis B 61 0.064
391
c THR037 Thrombocytopenia 2 36 0.064
392
BLS007 Blastic Plasmacytoid Dendritic Cell 41 0.064
393
P GLM007 Glomerulonephritis 56 0.064
394
LNG013 Lung Lymphoma 40 0.064
395
ALL026 Allergic Hypersensitivity Disease 53 0.063
396
MST017 Mast Cell Disease 52 0.063
397
WSC001 Wisconsin Syndrome 16 0.063
398
PLY125 Polycythemia Vera, Somatic 63 0.062
399
P NRV007 Nervous System Disease 71 0.062
400
c HPT001 Hepatitis C 68 0.062
401
CHR066 Chronic Fatigue Syndrome 63 0.062
402
SCT005 Scott Syndrome 51 0.062
403
BNM010 Bone Marrow Failure Syndrome 1 30 0.062
404
P ACT105 Acute Mountain Sickness 55 0.062
405
CNN005 Connective Tissue Disease 60 0.062
406
LYM051 Lymphomatoid Granulomatosis 46 0.062
407
HST016 Histiocytic Sarcoma 38 0.062
408
c CRN176 Coronary Heart Disease 9 19 0.062
409
WHT007 White Platelet Syndrome 17 0.062
410
DRM006 Dermatitis 58 0.061
411
RHB003 Rhabdomyosarcoma 55 0.061
412
P CND004 Candidiasis 58 0.061
413
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.061
414
FML039 Female Reproductive System Disease 49 0.061
415
HPT070 Hepatosplenic T-Cell Lymphoma 40 0.061
416
P ACT080 Acute Pulmonary Heart Disease 31 0.061
417
c SML023 Small Cell Lung Cancer, Adult 17 0.061
418
P MYC007 Myocardial Infarction 80 0.060
419
P INF032 Infertility 61 0.060
420
HYP066 Hyperglycemia 61 0.060
421
P HRP006 Herpes Simplex 65 0.060
422
OST003 Osteonecrosis 45 0.060
423
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 27 0.060
424
NWC001 Newcastle Disease 51 0.060
425
ANG046 Angioimmunoblastic T-Cell Lymphoma 42 0.060
426
P AMY004 Amyloidosis 63 0.060
427
MSC072 Muscle Cancer 47 0.060
428
P CNN004 Connective Tissue Cancer 44 0.060
429
c WLM005 Wilms Tumor 2 25 0.060
430
ENG004 Engraftment Syndrome 34 0.060
431
EWN003 Ewing Sarcoma 63 0.059
432
P TRC086 Trichohepatoenteric Syndrome 1 46 0.059
433
HRP004 Herpes Zoster 56 0.059
434
P PLY019 Polyneuropathy 53 0.059
435
P GRN010 Granular Cell Tumor 46 0.059
436
FLL019 Follicular Mucinosis 35 0.059
437
P ORG009 Organ System Cancer 45 0.059
438
P RNL014 Renal Cell Carcinoma 80 0.058
439
THR100 Thrombocytopenic Purpura, Autoimmune 53 0.058
440
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 36 0.058
441
PRP027 Peripheral Vascular Disease 69 0.058
442
P AST007 Astrocytoma 66 0.058
443
MRC001 Marchiafava Bignami Disease 33 0.058
444
PRC012 Pericardial Effusion 50 0.058
445
CLT003 Colitis 56 0.058
446
MTR008 Mature B-Cell Neoplasm 42 0.058
447
BRC012 Brucellosis 66 0.056
448
TST015 Testicular Disease 47 0.056
449
P PRP029 Porphyria 56 0.056
450
SFT003 Soft Tissue Sarcoma 55 0.056
451
HYP084 Hypopyon 29 0.056
452
IND005 Indolent B Cell Lymphoma 21 0.056
453
MND006 Mondor Disease 20 0.056
454
c SYS001 Systemic Lupus Erythematosus 87 0.055
455
P NJM001 Nijmegen Breakage Syndrome 68 0.055
456
VHW001 Vohwinkel Syndrome 47 0.055
457
c CNG401 Congenital Heart Disease 67 0.055
458
c HPT073 Hepatitis C Virus 72 0.055
459
P GLB002 Glioblastoma 65 0.055
460
FXF002 Fox-Fordyce Disease 37 0.055
461
c ACT027 Acute Pancreatitis 59 0.055
462
LYM020 Lymph Node Cancer 41 0.055
463
P END033 Endocarditis 52 0.055
464
YNG002 Young Syndrome 25 0.055
465
CYT008 Cytomegalovirus Infection 51 0.055
466
VSC001 Vascular Myelopathy 25 0.055
467
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 16 0.055
468
c HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.055
469
LYM116 Lymph Node Disease 42 0.055
470
NRN002 Neuronitis 40 0.055
471
SKN016 Skin Disease 69 0.054
472
P PRP003 Porphyria Cutanea Tarda 63 0.054
473
TST014 Testicular Cancer 55 0.054
474
TST021 Testicular Germ Cell Tumor 67 0.054
475
c PRM012 Primary Polycythemia 48 0.054
476
P LPS004 Lupus Erythematosus 63 0.054
477
ATR060 Atrial Standstill, Digenic 51 0.054
478
P ENC018 Encephalopathy 59 0.054
479
ZYG002 Zygomycosis 33 0.054
480
PYM001 Pyomyositis 39 0.054
481
c CNN010 Connective Tissue Benign Neoplasm 31 0.054
482
HYP025 Hyperphosphatemia 45 0.054
483
SPC003 Specific Developmental Disorder 39 0.054
484
FSR001 Fusariosis 31 0.054
485
DND018 Dendritic Cell Tumor 40 0.054
486
c ANP011 Anaplastic Small Cell Lymphoma 16 0.054
487
LYM041 Lymphocytes Absent 15 0.054
488
MN1001 Mn1 28 0.054
489
WLS001 Wilson Disease 72 0.053
490
SZR001 Sezary's Disease 51 0.053
491
LYM021 Lymphadenitis 58 0.053
492
ADM013 Adamantinoma of Long Bones 57 0.053
493
c THR048 Thrombocytopenia 4 29 0.053
494
P UVT001 Uveitis 60 0.053
495
P PLM006 Pulmonary Alveolar Proteinosis 46 0.053
496
P SDR003 Sideroblastic Anemia 40 0.053
497
PRT011 Protein C Deficiency 52 0.053
498
P THY023 Thymoma 57 0.053
499
CMP001 Composite Lymphoma 35 0.053
500
BCK006 Back Pain 40 0.053
501
PRM025 Primary Bacterial Infectious Disease 42 0.053
502
P MDL005 Medulloblastoma 76 0.052
503
OST085 Osteosarcoma, Somatic 63 0.052
504
P RSP003 Respiratory Failure 68 0.052
505
c NRF018 Neurofibromatosis, Type 1 69 0.052
506
PMP001 Pemphigus 49 0.052
507
c JVN003 Juvenile Xanthogranuloma 41 0.052
508
STT009 Sutton Disease 2 21 0.052
509
c ACT134 Acute Liver Failure 46 0.052
510
P GLM045 Glioma 53 0.052
511
CLN015 Colon Adenocarcinoma 55 0.052
512
P CRV039 Cervicitis 45 0.052
513
c SCN042 Secondary Hypereosinophilic Syndrome 15 0.052
514
KDN020 Kidney Cancer, Childhood 12 0.052
515
P ALX003 Alexander Disease 64 0.050
516
MLL018 Miller-Dieker Lissencephaly Syndrome 47 0.050
517
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.050
518
SKN023 Skin Tag 48 0.050
519
CTN014 Cutaneous Mastocytosis 49 0.050
520
TXC002 Toxic Encephalopathy 52 0.050
521
GST053 Gastric Cancer 52 0.050
522
CRB001 Cerebral Lymphoma 34 0.050
523
c PRM225 Primary Thrombocytopenia 42 0.050
524
HDG009 Hodgkin Lymphoma, Childhood 15 0.050
525
PRM133 Primary Pulmonary Lymphoma 24 0.050
526
P CLR023 Colorectal Cancer 96 0.049
527
c THR092 Thrombophilia Due to Thrombin Defect 56 0.049
528
URT039 Urticaria 58 0.049
529
NTR005 Nutritional Deficiency Disease 51 0.049
530
P LCT001 Lactic Acidosis 52 0.049
531
CRY004 Cryoglobulinemia 47 0.049
532
OST017 Osteomyelitis 60 0.049
533
MYC002 Mycobacterium Avium Complex Disease 52 0.049
534
TNS005 Tonsillitis 58 0.049
535
HYP017 Hypophosphatemia 43 0.049
536
c ACT075 Acute Myocardial Infarction 61 0.049
537
CHR208 Chromosome 17p Deletion 20 0.049
538
NVD002 Nevada Syndrome 15 0.049
539
c MNN043 Meningioma, Familial 61 0.048
540
CMR002 Coumarin Resistance 49 0.048
541
MSL001 Measles 61 0.048
542
P SNS014 Sinusitis 66 0.048
543
P GST049 Gastrointestinal System Cancer 59 0.048
544
HMR001 Hemorrhagic Thrombocythemia 47 0.048
545
PRP007 Priapism 48 0.048
546
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.048
547
HYP005 Hypokalemia 52 0.048
548
HPT022 Hepatoblastoma 57 0.048
549
GRN007 Granuloma Annulare 35 0.048
550
P EXN002 Exanthem 57 0.048
551
P LPS002 Liposarcoma 50 0.048
552
GLB003 Globe Disease 34 0.048
553
MYL052 Myeloproliferative Neoplasms, Familial 16 0.048
554
PRN049 Paraneoplastic Pemphigus 40 0.048
555
P NPH012 Nephrotic Syndrome 55 0.047
556
P HYP117 Hypertriglyceridemia 65 0.047
557
P MYP004 Myopathy 67 0.047
558
CHL067 Cholecystitis 57 0.047
559
P MYS005 Myositis 57 0.047
560
MRK001 Merkel Cell Carcinoma 56 0.047
561
TTH006 Tooth Disease 52 0.047
562
P ENC004 Encephalitis 60 0.047
563
RTN017 Retinal Detachment 58 0.047
564
PYD001 Pyoderma Gangrenosum 48 0.047
565
WRT001 Worth's Syndrome 37 0.047
566
OBS001 Obstructive Jaundice 47 0.047
567
ACC008 Accelerated Tumor Formation 20 0.047
568
P PLY041 Polymyositis 49 0.047
569
ANP010 Anaplastic Plasmacytoma 21 0.047
570
CHR062 Chronic Erythremia 15 0.047
571
c DLT001 Delta Chain Disease 14 0.047
572
PTR006 Peters Anomaly 64 0.045
573
MVD001 Moved to 60 0.045
574
WLL001 Williams-Beuren Syndrome 61 0.045
575
c ART101 Aortic Valve Disease 2 56 0.045
576
INS024 Insulin-Like Growth Factor I 75 0.045
577
VRL011 Viral Infectious Disease 56 0.045
578
MLL012 Miller Syndrome 43 0.045
579
P ART023 Arthropathy 63 0.045
580
APP008 Appendicitis 61 0.045
581
SCB001 Scabies 45 0.045
582
TMP012 Temple Syndrome 39 0.045
583
P ANT006 Antiphospholipid Syndrome 60 0.045
584
MMB001 Membranoproliferative Glomerulonephritis 44 0.045
585
DND002 Dendritic Cell Sarcoma 44 0.045
586
CYT004 Cytomegalic Inclusion Disease 29 0.045
587
PNN001 Panniculitis 47 0.045
588
P TRT010 Teratoma 49 0.045
589
MLG041 Malignant Triton Tumor 35 0.045
590
P HVY001 Heavy Chain Disease 41 0.045
591
CHR276 Chronic Active Epstein-Barr Virus Infection 45 0.045
592
ECT004 Ecthyma 37 0.045
593
TTR021 Tetrasomy 21 20 0.045
594
c TCL008 T-Cell Lymphoma 1a 17 0.045
595
CYC007 Cyclic Thrombocytopenia 37 0.045
596
GLM011 Glomerulosclerosis 41 0.045
597
OTP003 Oto-Palatal-Digital Syndrome 14 0.045
598
THY028 Thyroid Cancer 71 0.044
599
CNT098 Central Core Disease 68 0.044
600
NTR040 Neutropenia, Cyclic 51 0.044
601
ULC004 Ulcerative Colitis 74 0.044
602
GLB001 Gilbert Syndrome 59 0.044
603
CMM004 Common Variable Immunodeficiency 68 0.044
604
P PTS002 Ptosis 56 0.044
605
MST006 Mast Syndrome 44 0.044
606
MGL001 Megaloblastic Anemia 51 0.044
607
SPN040 Spinal Cancer 43 0.044
608
ALP008 Alopecia 56 0.044
609
P HYP076 Hyperthyroidism 59 0.044
610
CHP002 Chops Syndrome 36 0.044
611
CNV002 Conversion Disorder 45 0.044
612
P HML001 Hemolytic-Uremic Syndrome 50 0.044
613
NTR018 Neutrophilia, Hereditary 32 0.044
614
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.044
615
P FNC004 Fanconi Syndrome 54 0.044
616
CLC006 Calcinosis 48 0.044
617
PYD002 Pyoderma 46 0.044
618
c RNG017 Ring Chromosome 21 25 0.044
619
P LRY019 Laryngitis 55 0.044
620
CRD001 Cardiac Tamponade 43 0.044
621
P SKN013 Skin Benign Neoplasm 38 0.044
622
AGG002 Aggressive Systemic Mastocytosis 42 0.044
623
TRS012 Trisomy 22 26 0.044
624
EXT010 Extramedullary Plasmacytoma 49 0.044
625
HST009 Histiocytoma 47 0.044
626
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 41 0.044
627
P HNT016 Huntington Disease 80 0.042
628
P LVR013 Liver Disease 76 0.042
629
CNG034 Congestive Heart Failure 72 0.042
630
P PLM037 Pulmonary Hypertension 78 0.042
631
ABT001 Abetalipoproteinemia 60 0.042
632
P FND001 Fundus Albipunctatus 52 0.042
633
RPP001 Rapp-Hodgkin Syndrome 52 0.042
634
SPN060 Spondylocarpotarsal Synostosis Syndrome 38 0.042
635
c JVN010 Juvenile Rheumatoid Arthritis 65 0.042
636
PLY119 Polymicrogyria, Bilateral Perisylvian 31 0.042
637
HYP299 Hyperostosis, Endosteal 45 0.042
638
MYX005 Myxoid Liposarcoma 58 0.042
639
EMN001 Emanuel Syndrome 38 0.042
640
NSD001 Nose Disease 51 0.042
641
ANG049 Angioedema Induced by Ace Inhibitors 35 0.042
642
KLN001 Klinefelter's Syndrome 52 0.042
643
AMN001 Amenorrhea 51 0.042
644
GYN001 Gynecomastia 49 0.042
645
c THR090 Thrombocythemia 1 36 0.042
646
CLL003 Cellulitis 49 0.042
647
6MR001 6-Mercaptopurine Sensitivity 24 0.042
648
CLR062 Colorblindness, Protan 17 0.042
649
SPR035 Superior Vena Cava Syndrome 31 0.042
650
CYT005 Cytomegalovirus Retinitis 48 0.042
651
PRT038 Protein-Energy Malnutrition 48 0.042
652
MST004 Mast Cell Neoplasm 40 0.042
653
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 22 0.042
654
MLG097 Malignant Mesenchymal Tumor 36 0.042
655
PRL008 Paralytic Ileus 37 0.042
656
GNR023 Generalized Eruptive Histiocytosis 21 0.042
657
HNM002 Hinman Syndrome 22 0.042
658
PRT026 Parotitis 42 0.042
659
PTT004 Pituitary Apoplexy 38 0.042
660
PRM128 Primary Cutaneous Follicle Center Lymphoma 25 0.042
661
c EYL003 Eye Lymphoma 33 0.042
662
LYM045 Lymphocytic Vasculitis 35 0.042
663
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 19 0.042
664
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 21 0.042
665
ANG037 Angiomatosis 33 0.042
666
GST078 Gastrointestinal Allergy 41 0.042
667
c FML303 Familial/multiple Cancer 15 0.042
668
P MYS003 Myasthenia Gravis 64 0.041
669
c INF071 Inflammatory Bowel Disease 1 51 0.041
670
P ALP009 Alopecia Areata 62 0.041
671
P GT001 Gout 58 0.041
672
STR008 Strongyloidiasis 51 0.041
673
RSC001 Rosacea 54 0.041
674
SPT004 Septic Arthritis 60 0.041
675
LST001 Listeriosis 53 0.041
676
P ESP024 Esophagitis 62 0.041
677
P MMP001 Mumps 56 0.041
678
c ALM001 Al Amyloidosis 45 0.041
679
GLB015 Glioblastoma Multiforme 63 0.041
680
VSC003 Visceral Leishmaniasis 56 0.041
681
THY030 Thyroid Gland Disease 52 0.041
682
P INT063 Intellectual Disability 46 0.041
683
MXD005 Mixed Connective Tissue Disease 63 0.041
684
P AVS004 Avascular Necrosis of the Femoral Head 55 0.041
685
PRN011 Pernicious Anemia 41 0.041
686
INT067 Interstitial Nephritis 48 0.041
687
ADN018 Adenoma 59 0.041
688
STM007 Stomatitis 50 0.041
689
P AGM001 Agammaglobulinemia 63 0.041
690
EPG003 Epiglottitis 32 0.041
691
NRW001 Norwegian Scabies 31 0.041
692
HYP063 Hypersplenism 49 0.041
693
SPL006 Splenic Infarction 32 0.041
694
URT008 Urticaria Pigmentosa 37 0.041
695
PLR008 Pleurisy 51 0.041
696
ISC004 Ischemia 56 0.041
697
HDR003 Hidradenitis 46 0.041
698
FSC004 Fasciitis 47 0.041
699
PHY002 Physical Disorder 43 0.041
700
c MLG081 Malignant Teratoma 46 0.041
701
P CPL003 Capillary Leak Syndrome 42 0.041
702
TCL003 T Cell Deficiency 44 0.041
703
TST004 Testicular Lymphoma 34 0.041
704
THY009 Thyroid Lymphoma 48 0.041
705
PRN039 Paraneoplastic Syndromes 42 0.041
706
BRN049 Brain Tumor, Childhood 15 0.041
707
INC002 Inclusion Body Myositis 64 0.039
708
P OVR042 Ovarian Cancer 73 0.039
709
P PFF001 Pfeiffer Syndrome 73 0.039
710
KPS004 Kaposi Sarcoma 69 0.039
711
KRT004 Keratitis 70 0.039
712
BLM001 Bloom Syndrome 63 0.039
713
CRH001 Crohn's Disease 76 0.039
714
KRT002 Keratomalacia 50 0.039
715
P FCL005 Focal Segmental Glomerulosclerosis 59 0.039
716
P PSR002 Psoriasis 63 0.039
717
EPD001 Epidermodysplasia Verruciformis 48 0.039
718
MYL013 Myeloperoxidase Deficiency 46 0.039
719
c MCR115 Microvascular Complications of Diabetes 5 60 0.039
720
P HMP007 Hemophilia 55 0.039
721
P LYM025 Lymphedema 60 0.039
722
ORL005 Oral Candidiasis 47 0.039
723
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.039
724
CRN036 Craniopharyngioma 54 0.039
725
CRS005 Crest Syndrome 37 0.039
726
P DRR001 Diarrhea 60 0.039
727
P OLG002 Oligodendroglioma 55 0.039
728
P HYP014 Hyperuricemia 49 0.039
729
BRN012 Bronchiolitis Obliterans 58 0.039
730
PRC013 Pericarditis 52 0.039
731
P SML001 Small Cell Carcinoma 54 0.039
732
c THR087 Thrombocythemia 2 25 0.039
733
LYM052 Lymphomatoid Papulosis 45 0.039
734
MNN042 Meningioma, Radiation-Induced 22 0.039
735
ORB012 Orbital Cancer 32 0.039
736
BRN002 Bronchiolitis 56 0.039
737
NNN007 Non-Involuting Congenital Hemangioma 17 0.039
738
GRW007 Growth Hormone Deficiency 49 0.039
739
ANR040 Aneurysm 56 0.039
740
P LMY004 Leiomyosarcoma 54 0.039
741
INT054 Intraocular Lymphoma 46 0.039
742
ACL001 Acalculous Cholecystitis 35 0.039
743
PPL002 Papillary Carcinoma 50 0.039
744
WDS002 Woods Syndrome 30 0.039
745
MYC017 Mycobacterium Kansasii 40 0.039
746
PNM003 Pneumatosis Cystoides Intestinalis 32 0.039
747
P SML002 Small Cell Sarcoma 39 0.039
748
c ALX006 Alexander Disease Type Ii 17 0.039
749
c ALX007 Alexander Disease Type I 17 0.039
750
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.039
751
CNT067 Central Cord Syndrome 22 0.039
752
c SLC031 Slco1b1-Related Altered Drug Metabolism 10 0.039
753
P RTT002 Rett Syndrome 77 0.037
754
P HMC003 Hemochromatosis 71 0.037
755
P RBN001 Rubinstein-Taybi Syndrome 65 0.037
756
P BCK002 Beckwith-Wiedemann Syndrome 56 0.037
757
P ADD001 Addison's Disease 60 0.037
758
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 77 0.037
759
HST011 Histoplasmosis 54 0.037
760
P ANR007 Anorexia Nervosa 63 0.037
761
SLP005 Sleep Disorder 52 0.037
762
P SML016 Small Intestine Cancer 54 0.037
763
PPL021 Papilledema 47 0.037
764
HYP056 Hypoglycemia 60 0.037
765
ETN001 Eating Disorder 59 0.037
766
GRN016 Grant Syndrome 30 0.037
767
c PND001 Pain Disorder 53 0.037
768
c THR102 Thrombocytopenia 5 29 0.037
769
AYM001 Ayme-Gripp Syndrome 40 0.037
770
EMB004 Embryonal Carcinoma 55 0.037
771
P CRN035 Cranial Nerve Palsy 44 0.037
772
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.037
773
END030 End Stage Renal Failure 53 0.037
774
GRD007 Grade Iii Astrocytoma 50 0.037
775
c GMM003 Gamma Heavy Chain Disease 46 0.037
776
c CTR122 Cataract 5, Multiple Types 30 0.037
777
FLR002 Filariasis 55 0.037
778
LPR001 Lepromatous Leprosy 50 0.037
779
CLD007 Cold Agglutinin Disease 44 0.037
780
DDN006 Duodenitis 44 0.037
781
MLR002 Miliary Tuberculosis 39 0.037
782
P BRS044 Breast Adenocarcinoma 58 0.037
783
EMP001 Empty Sella Syndrome 39 0.037
784
INT253 Intestinal Benign Neoplasm 48 0.037
785
HYP085 Hypothalamic Disease 43 0.037
786
P END047 Endophthalmitis 46 0.037
787
P SCL015 Scleritis 49 0.037
788
FML037 Female Breast Cancer 49 0.037
789
c ACQ014 Acquired Hemophilia 42 0.037
790
MMB002 Membranous Glomerulonephritis 47 0.037
791
RTN001 Retinal Vasculitis 43 0.037
792
PLY010 Polyclonal Hypergammaglobulinemia 31 0.037
793
CHR008 Choroiditis 43 0.037
794
SGT001 Sagittal Sinus Thrombosis 32 0.037
795
NVS004 Nova Syndrome 18 0.037
796
MDS019 Mediastinal Malignant Lymphoma 36 0.037
797
P DMY001 Demyelinating Polyneuropathy 41 0.037
798
PLY020 Polyradiculoneuropathy 42 0.037
799
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.037
800
SPL007 Splenic Abscess 35 0.037
801
PHY001 Physiological Polycythemia 31 0.037
802
MNT045 Montefiore Syndrome 11 0.037
803
P STM004 Stomach Cancer 73 0.036
804
MLR004 Malaria 80 0.036
805
P OST002 Osteoporosis 63 0.036
806
P CNT061 Conotruncal Heart Malformations 61 0.036
807
ACN011 Acne 63 0.036
808
P CLD001 Cleidocranial Dysplasia 62 0.036
809
P WVR001 Weaver Syndrome 54 0.036
810
SHW002 Shwachman-Diamond Syndrome 59 0.036
811
ACR007 Acromegaly 66 0.036
812
CRD119 Cardiac Arrest 63 0.036
813
PYR013 Pyruvate Kinase Deficiency 58 0.036
814
GLL022 Guillain-Barre Syndrome 58 0.036
815
WHM001 Whim Syndrome 53 0.036
816
c MTB001 Metabolic Syndrome X 61 0.036
817
TTN003 Tetanus 62 0.036
818
NCR004 Nocardiosis 44 0.036
819
ADP007 Adie Pupil 33 0.036
820
CHR012 Chronic Granulomatous Disease 66 0.036
821
MLN012 Melanoma and Neural System Tumor Syndrome 27 0.036
822
OLV001 Olivopontocerebellar Atrophy 53 0.036
823
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 32 0.036
824
PLN006 Poland Syndrome 48 0.036
825
SVN001 Sveinsson Choreoretinal Atrophy 28 0.036
826
P PLC011 Pilocytic Astrocytoma 59 0.036
827
ACQ007 Acquired Immunodeficiency Syndrome 60 0.036
828
P PRT013 Portal Hypertension 61 0.036
829
PRP016 Paraplegia 49 0.036
830
OCL022 Ocular Melanoma 53 0.036
831
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.036
832
P THR015 Thrombophilia 59 0.036
833
P LPR002 Leopard Syndrome 53 0.036
834
P HYP083 Hypopituitarism 50 0.036
835
P CTR002 Cataract 57 0.036
836
RDN001 Reading Disorder 39 0.036
837
PST062 Pustulosis Palmaris Et Plantaris 48 0.036
838
GST027 Gastric Lymphoma 54 0.036
839
LYM027 Lymphopenia 54 0.036
840
ANR004 Anuria 46 0.036
841
P CMP008 Compartment Syndrome 46 0.036
842
DSM007 Desmoplastic Small Round Cell Tumor 49 0.036
843
INT038 Interdigitating Dendritic Cell Sarcoma 35 0.036
844
P SPR013 Spiradenoma 37 0.036
845
P PNV001 Panuveitis 50 0.036
846
XLN215 X-Linked Congenital Generalized Hypertrichosis 18 0.036
847
INF034 Infective Endocarditis 50 0.036
848
MCP006 Mucoepidermoid Carcinoma 50 0.036
849
CHR463 Chronic Actinic Dermatitis 33 0.036
850
LKP003 Leukoplakia 44 0.036
851
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 37 0.036
852
BCL002 B Cell Deficiency 50 0.036
853
PYG006 Pyogenic Granuloma 47 0.036
854
BCL011 Bacillary Angiomatosis 25 0.036
855
ANP009 Anaplastic Oligodendroglioma 37 0.036
856
MYC014 Mycobacterium Chelonae 32 0.036
857
DSC004 Discitis 23 0.036
858
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.036
859
MLN003 Melancholia 36 0.036
860
CRB026 Cerebellar Astrocytoma 39 0.036
861
SML008 Small Intestine Lymphoma 43 0.036
862
c RNL016 Renal Infectious Disease 22 0.036
863
VRS001 Virus Associated Hemophagocytic Syndrome 34 0.036
864
MSC004 Muscle Tissue Disease 35 0.036
865
TST022 Testicular Cancer, Childhood 13 0.036
866
ESP021 Esophageal Cancer 75 0.034
867
DCH001 Duchenne Muscular Dystrophy 81 0.034
868
CHD001 Chediak-Higashi Syndrome 66 0.034
869
P TRN020 Turner Syndrome 64 0.034
870
P TMP003 Temporal Arteritis 61 0.034
871
SML033 Small Cell Cancer of the Lung, Somatic 53 0.034
872
LSH001 Leishmaniasis 63 0.034
873
CLD014 Cole Disease 38 0.034
874
THR016 Thrombophlebitis 55 0.034
875
P MSC005 Muscular Dystrophy 64 0.034
876
ABL002 Ablepharon-Macrostomia Syndrome 51 0.034
877
ERY003 Erythema Multiforme 57 0.034
878
ACN002 Acanthosis Nigricans 59 0.034
879
c BSL007 Basal Cell Carcinoma 66 0.034
880
P ADL010 Adult Respiratory Distress Syndrome 60 0.034
881
c HPT003 Hepatitis a 55 0.034
882
TNG003 Tongue Cancer 59 0.034
883
PRL009 Prolactinoma 63 0.034
884
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 28 0.034
885
P CRD011 Cardiomyopathy 66 0.034
886
ECT026 Ectopic Pregnancy 46 0.034
887
c VRL010 Viral Hepatitis 60 0.034
888
P CYS018 Cystitis 54 0.034
889
MYL057 Myelopathy, Htlv-1-Associated 28 0.034
890
P SLP006 Sleep Apnea 60 0.034
891
DFF027 Diffuse Lymphatic Malformation 28 0.034
892
P FBR017 Fibrosarcoma 55 0.034
893
HPT014 Hepatorenal Syndrome 47 0.034
894
CNG028 Congenital Hypoplastic Anemia 48 0.034
895
END021 Endomyocardial Fibrosis 47 0.034
896
HDC001 Headache 52 0.034
897
MCR017 Macrocytic Anemia 43 0.034
898
P EPL164 Epilepsy 60 0.034
899
MYL002 Myelophthisic Anemia 33 0.034
900
CRH005 Crohn's Colitis 50 0.034
901
MDS018 Mediastinal Cancer 34 0.034
902
END040 Endogenous Depression 51 0.034
903
PLM012 Pulmonary Sarcoidosis 54 0.034
904
CRB040 Cerebrum Cancer 36 0.034
905
GNG002 Ganglioneuroma 41 0.034
906
FBR003 Fibrous Histiocytoma 46 0.034
907
TBR011 Tuberculous Meningitis 46 0.034
908
EWN002 Ewing's Family of Tumors 45 0.034
909
CCC002 Coccidiosis 49 0.034
910
HMN032 Human Herpesvirus 8 42 0.034
911
KLD001 Keloids 50 0.034
912
FLL008 Folliculitis 47 0.034
913
PRV003 Perivascular Epithelioid Cell Tumor 38 0.034
914
SXD001 Sex Differentiation Disease 39 0.034
915
c CRN175 Coronary Heart Disease 4 19 0.034
916
BNM008 Bone Mineral Density, Low 28 0.034
917
BRS001 Breast Lymphoma 31 0.034
918
c CNG031 Congenital Nervous System Abnormality 39 0.034
919
IDP064 Idiopathic Neutropenia 43 0.034
920
IMM001 Immune-Complex Glomerulonephritis 41 0.034
921
c ANT023 Anterior Scleritis 37 0.034
922
HMR023 Hemorrhagic Cystitis 33 0.034
923
MXD032 Mixed Germ Cell Tumor 31 0.034
924
THR035 Thrombasthenia 41 0.034
925
c HYP595 Hypertension, Essential 69 0.032
926
SCK003 Sickle Cell Anemia 72 0.032
927
P FML161 Familial Mediterranean Fever, Ar 64 0.032
928
c INF069 Infantile Neuroaxonal Dystrophy 1 44 0.032
929
P NNN008 Noonan Syndrome 1 64 0.032
930
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.032
931
WRN001 Werner Syndrome 69 0.032
932
SMT008 Smith-Magenis Syndrome 49 0.032
933
c FNC027 Fanconi Anemia, Complementation Group a 71 0.032
934
P NMN002 Niemann-Pick Disease 63 0.032
935
P DYS007 Dyskeratosis Congenita 64 0.032
936
P KBK002 Kabuki Syndrome 1 49 0.032
937
CRN237 Corneal Dystrophy, Avellino Type 31 0.032
938
P URF003 Urofacial Syndrome 1 51 0.032
939
PTT046 Pituitary Hormone Deficiency, Combined, 2 54 0.032
940
P BDD001 Budd-Chiari Syndrome 52 0.032
941
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 42 0.032
942
P CNJ013 Conjunctivitis 65 0.032
943
RCT018 Rectal Neoplasm 53 0.032
944
IMM104 Immunodeficiency with Hyper-Igm, Type 2 31 0.032
945
GST023 Gastric Ulcer 56 0.032
946
GNT031 Genitopatellar Syndrome 41 0.032
947
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.032
948
URN009 Urinary System Disease 52 0.032
949
P HYP086 Hypothyroidism 63 0.032
950
THR013 Thoracic Outlet Syndrome 48 0.032
951
ATP002 Atopy 62 0.032
952
ICH054 Ichthyosis, X-Linked 46 0.032
953
P GRV001 Graves' Disease 62 0.032
954
P INT070 Intestinal Obstruction 55 0.032
955
MCN017 Meconium Ileus 53 0.032
956
c CRN159 Craniosynostosis, Type 1 33 0.032
957
QFV001 Q Fever 62 0.032
958
EXF001 Exfoliation Syndrome 56 0.032
959
TNG009 Tongue Squamous Cell Carcinoma 73 0.032
960
PRK066 Parkinsonism with Spasticity, X-Linked 24 0.032
961
CRV047 Cervical Cancer, Somatic 65 0.032
962
c IRD008 Iridogoniodysgenesis, Type 2 31 0.032
963
PLS007 Plasmodium Falciparum Malaria 56 0.032
964
FLT011 Felty Syndrome 48 0.032
965
P HRD001 Hereditary Multiple Exostoses 46 0.032
966
P ARC016 Auriculocondylar Syndrome 1 44 0.032
967
LMB002 Lambert-Eaton Myasthenic Syndrome 47 0.032
968
EST005 Esotropia 39 0.032
969
TXC005 Toxic Shock Syndrome 61 0.032
970
CRY005 Cryptococcosis 50 0.032
971
c ATM011 Autoimmune Hepatitis 62 0.032
972
ERD001 Erdheim-Chester Disease 51 0.032
973
PLM010 Pulmonary Edema 56 0.032
974
APH002 Aphasia 52 0.032
975
P ANG015 Angioedema 53 0.032
976
TRP014 Triploidy 39 0.032
977
CDQ001 Cauda Equina Syndrome 40 0.032
978
DWR001 Dwarfism 42 0.032
979
HYP068 Hyperostosis 39 0.032
980
FCT005 Factor Xiii Deficiency 42 0.032
981
SKN027 Skin Conditions 44 0.032
982
LNS003 Lens Disease 37 0.032
983
OLG006 Oligoastrocytoma 33 0.032
984
P PLN008 Peeling Skin Syndrome 45 0.032
985
c PSR019 Psoriasis Susceptibility 13 24 0.032
986
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.032
987
c HPT007 Hepatitis E 51 0.032
988
BRN014 Bronchopneumonia 45 0.032
989
NCR007 Necrotizing Fasciitis 43 0.032
990
PSR005 Psoriasis, Protection Against 18 0.032
991
MLR007 Male Reproductive System Disease 36 0.032
992
ACT084 Acute Stress Disorder 38 0.032
993
LTT002 Letterer-Siwe Disease 32 0.032
994
HYD002 Hydronephrosis 48 0.032
995
LNG004 Langerhans Cell Sarcoma 35 0.032
996
SPN026 Spinal Cord Lymphoma 25 0.032
997
P MTH007 Methemoglobinemia 44 0.032
998
c FML108 Familial Breast Cancer 58 0.032
999
ORL019 Oral Hairy Leukoplakia 33 0.032
1000
c HRD009 Hereditary Wilms' Tumor 40 0.032
1001
c WLM011 Wilms Tumor 6 20 0.032
1002
ATY005 Atypical Teratoid Rhabdoid Tumor 47 0.032
1003
HHV001 Hhv-6 Encephalitis 16 0.032
1004
c BKV001 Bk-Virus Nephropathy 24 0.032
1005
P GNT008 Giant Cell Tumor 51 0.032
1006
EPT020 Epithelioid Hemangioendothelioma 46 0.032
1007
EXF003 Exfoliative Dermatitis 25 0.032
1008
HPT002 Hepatic Vein Thrombosis 38 0.032
1009
HYP391 Hyperammonemia 38 0.032
1010
c CNT016 Central Retinal Vein Occlusion 34 0.032
1011
GRM001 Germ Cell and Embryonal Cancer 38 0.032
1012
CRB036 Cerebral Meningioma 39 0.032
1013
MNN009 Meningoencephalitis 42 0.032
1014
CRY014 Cryptococcal Meningitis 41 0.032
1015
GLC008 Glucose Metabolism Disease 44 0.032
1016
ANP008 Anaplastic Oligoastrocytoma 23 0.032
1017
PTT037 Pituitary Tumors 45 0.032
1018
RCM004 Recombinant 8 Syndrome 17 0.032
1019
CRB002 Cerebral Primitive Neuroectodermal Tumor 42 0.032
1020
PLY021 Polyradiculopathy 25 0.032
1021
MNC004 Monoclonal Paraproteinemia 35 0.032
1022
P RTN022 Retinal Vein Occlusion 36 0.032
1023
GNG006 Gingival Hypertrophy 29 0.032
1024
BRN021 Brain Sarcoma 30 0.032
1025
LVR006 Liver Lymphoma 29 0.032
1026
LMB024 Limbic Encephalitis 35 0.032
1027
PRR008 Periarteritis Nodosa 28 0.032
1028
WBR001 Weber Syndrome 36 0.032
1029
c ABC018 Abcb1-Related Altered Drug Metabolism 11 0.032
1030
EMB007 Embryonal Sarcoma 45 0.032
1031
BNF002 Bone Fracture 46 0.032
1032
VSC047 Vascular Malformation 45 0.032
1033
FST010 Fasting Hypoglycemia 37 0.032
1034
P SCH015 Schizophrenia 78 0.030
1035
P AST005 Asthma 80 0.030
1036
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.030
1037
ADN021 Adenomatous Polyposis Coli 71 0.030
1038
P CRN211 Coronary Artery Disease 74 0.030
1039
ANX002 Anxiety Disorder 67 0.030
1040
FML011 Familial Adenomatous Polyposis 68 0.030
1041
P WSK001 Wiskott-Aldrich Syndrome 70 0.030
1042
P LPR003 Leprosy 70 0.030
1043
ACH004 Achondroplasia 64 0.030
1044
P PLR004 Pleuropulmonary Blastoma 63 0.030
1045
P ICH001 Ichthyosis Vulgaris 44 0.030
1046
P ERY008 Erythromelalgia 50 0.030
1047
P DMN001 Diamond-Blackfan Anemia 69 0.030
1048
P PRC019 Precocious Puberty 53 0.030
1049
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 54 0.030
1050
MLD001 Melioidosis 67 0.030
1051
MLK003 Melkersson-Rosenthal Syndrome 52 0.030
1052
c CHR089 Chronic Kidney Failure 67 0.030
1053
NRF008 Neurofibromatosis-Noonan Syndrome 45 0.030
1054
P DRM010 Dermatomyositis 59 0.030
1055
TRS007 Trismus-Pseudocamptodactyly Syndrome 33 0.030