Search results for "leukemia"

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

3647 hits were found for 'leukemia'

# Family MCID Name MIFTS Score
1
c LKM062 Leukemia, Acute Lymphoblastic 64 8.068
2
c LKM061 Leukemia, Acute Myeloid 73 6.906
3
c CHR090 Chronic Lymphocytic Leukemia 76 6.885
4
P LKM002 Leukemia 71 6.856
5
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 6.819
6
LKM067 Leukemia, Acute Promyelocytic, Somatic 52 5.441
7
P MYL006 Myeloid Leukemia 66 5.074
8
MGK001 Megakaryocytic Leukemia 55 4.843
9
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 60 4.732
10
c ACT073 Acute Leukemia 60 4.482
11
c ACT009 Acute Monocytic Leukemia 52 4.270
12
HRY003 Hairy Cell Leukemia 57 4.250
13
ACT216 Acute Leukemia of Ambiguous Lineage 34 4.247
14
P LYM026 Lymphoblastic Leukemia 62 4.117
15
c ADL017 Adult T-Cell Leukemia 60 4.079
16
ATY042 Atypical Chronic Myeloid Leukemia 48 4.007
17
c LKM060 Leukemia, Acute Lymphoblastic 3 50 3.994
18
NTR003 Natural Killer Cell Leukemia 47 3.908
19
P ACT074 Acute Lymphocytic Leukemia 56 3.835
20
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 3.731
21
ACT103 Acute Lymphoblastic Leukemia, Childhood 41 3.700
22
CHR285 Chronic Myelomonocytic Leukemia 56 3.579
23
ACT200 Acute Monoblastic Leukemia 42 3.483
24
P TCL004 T-Cell Leukemia 47 3.382
25
c ACT020 Acute T Cell Leukemia 35 3.376
26
c TCL005 T-Cell Prolymphocytic Leukemia 52 3.233
27
c ADL052 Adult Acute Lymphocytic Leukemia 44 3.231
28
P MNC007 Monocytic Leukemia 55 3.167
29
c CHR418 Chronic Leukemia 47 3.155
30
ACT098 Acute Erythroid Leukemia 47 3.114
31
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 3.099
32
c CHR064 Chronic Monocytic Leukemia 42 3.002
33
ACT113 Acute Myeloblastic Leukemia with Maturation 37 2.923
34
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 17 2.891
35
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 2.855
36
PLS016 Plasma Cell Leukemia 42 2.850
37
CHL061 Childhood Leukemia 49 2.825
38
PRL017 Prolymphocytic Leukemia 47 2.806
39
TCL002 T-Cell Large Granular Lymphocyte Leukemia 42 2.803
40
MST002 Mast-Cell Leukemia 48 2.786
41
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 2.749
42
LRG008 Large Granular Lymphocyte Leukemia 39 2.713
43
LYM067 Lymphoid Leukemia 44 2.703
44
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 2.698
45
NNN022 Noonan Syndrome-Like Disorder with or Without Juvenile Myelomonocytic Leukemia 28 2.638
46
c LKM005 Leukemia, T-Cell, Chronic 20 2.636
47
CNT018 Central Nervous System Leukemia 37 2.528
48
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 22 2.505
49
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 14 2.431
50
ACT118 Acute Non Lymphoblastic Leukemia 30 2.396
51
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 24 2.394
52
c LKM055 Leukemia, Acute Lymphoblastic 2 19 2.385
53
c LKM004 Leukemia, B-Cell, Chronic 24 2.383
54
CHR286 Chronic Neutrophilic Leukemia 43 2.364
55
c LKM056 Leukemia, Chronic Lymphocytic 2 21 2.354
56
c LKM050 Leukemia, Chronic Lymphocytic 1 19 2.341
57
P BCL005 B Cell Prolymphocytic Leukemia 43 2.327
58
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 34 2.326
59
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 27 2.292
60
PLS003 Plasmacytic Leukemia 21 2.270
61
c LKM051 Leukemia, Chronic Lymphocytic 3 19 2.244
62
SBL003 Subleukemic Leukemia 10 2.171
63
NLL001 Null-Cell Leukemia 30 2.164
64
c ADL093 Adult Acute Monocytic Leukemia 19 2.120
65
CHR563 Chronic Eosinophilic Leukemia 46 2.084
66
P CHR562 Chronic Myelocytic Leukemia 41 2.077
67
CRB138 Core Binding Factor Acute Myeloid Leukemia 42 2.017
68
ACT095 Acute Biphenotypic Leukemia 32 2.003
69
ALK003 Aleukemic Leukemia Cutis 31 1.970
70
RFR002 Refractory Hairy Cell Leukemia 29 1.969
71
TST003 Testicular Leukemia 31 1.963
72
ERY051 Erythroleukemia, Familial 23 1.918
73
NNT007 Neonatal Leukemia 35 1.916
74
ACT222 Acute Pre-B-Cell Lymphoblastic Leukemia 20 1.909
75
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 22 1.907
76
MYL055 Myeloid/lymphoid or Mixed Lineage Leukemia 29 1.890
77
ALK002 Aleukemic Monocytic Leukemia Cutis 9 1.881
78
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 30 1.877
79
SPL013 Splenic Manifestation of Leukemia 14 1.877
80
CBP001 Cebpa-Associated Familial Acute Myeloid Leukemia 5 1.865
81
CLL014 Cll/sll 42 1.798
82
ACT177 Acute Basophilic Leukemia 34 1.705
83
LYM040 Lymphoblastic Lymphoma 53 1.700
84
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 18 1.674
85
BND002 B- and T-Cell Mixed Leukemia 17 1.619
86
PDT026 Pediatric T-Cell Leukemia 11 1.619
87
ACT234 Acute Myeloid Leukemia with Minimal Differentiation 22 1.590
88
AML051 Aml with Myelodysplasia-Related Features 18 1.588
89
ACT224 Acute Promyelocytic Leukemia Pml/rara Type 10 1.588
90
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 12 1.577
91
c ACT219 Acute Myeloid Leukemia, Flt3-Related 29 1.558
92
c SBC006 Subacute Leukemia 11 1.558
93
P 8P1002 8p11 Myeloproliferative Syndrome 36 1.551
94
P JVN054 Juvenile Myelomonocytic Leukemia, Somatic Arhgap26-Related 11 1.551
95
c FML328 Familial Chronic Myelocytic Leukemia-Like Syndrome 8 1.545
96
c SBC015 Subacute Monocytic Leukemia 11 1.541
97
c INH015 Inherited Acute Myeloid Leukemia 25 1.533
98
ACT196 Acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2) 8 1.533
99
c HMN021 Human T-Cell Leukemia Virus Type 1 52 1.532
100
SPL010 Splenic Manifestation of Hairy Cell Leukemia 12 1.528
101
CHL029 Childhood Precursor T-Lymphoblastic Lymphoma/leukemia 11 1.528
102
ACT223 Acute Promyelocytic Leukemia Numa/rara Type 5 1.528
103
PRG005 Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 7 1.523
104
PST004 Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 7 1.523
105
FML045 Familial Mosaic Monosomy 7 Syndrome 7 1.523
106
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 15 1.397
107
c HMN022 Human T-Cell Leukemia Virus Type 2 44 1.209
108
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 13 1.192
109
NSY001 N Syndrome 36 1.189
110
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 12 1.173
111
THR106 Therapy Related Acute Myeloid Leukemia and Myelodysplastic Syndrome 14 1.169
112
ACT217 Acute Myeloid Leukemia with Recurrent Genetic Anomaly 10 1.159
113
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 22 1.148
114
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 26 1.136
115
c HMN023 Human T-Cell Leukemia Virus Type 3 14 1.133
116
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 24 1.127
117
P LFR001 Li-Fraumeni Syndrome 75 1.125
118
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 14 1.125
119
PRC009 Precursor T-Lymphoblastic Lymphoma/leukemia Refractory 11 1.115
120
ALK014 Aleukemic Mast Cell Leukemia 10 1.115
121
c JVN055 Juvenile Myelomonocytic Leukemia, Somatic Cbl-Related 8 1.115
122
c JVN056 Juvenile Myelomonocytic Leukemia, Somatic Nf1-Related 8 1.115
123
c JVN057 Juvenile Myelomonocytic Leukemia, Somatic Ptpn11-Related 8 1.115
124
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 25 1.111
125
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 14 1.111
126
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 31 1.108
127
c ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 28 1.108
128
DFN299 Deafness-Lymphedema-Leukemia Syndrome 10 1.108
129
c MYL058 Myeloproliferative Syndrome, Transient 33 1.104
130
c ACT198 Acute Myeloid Leukemia with T(6;9)(p23;q34) 17 1.104
131
BLN016 Bilineal Acute Leukemia 9 1.104
132
P ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 16 1.099
133
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 9 1.099
134
EMB016 Emberger Syndrome 28 1.095
135
UNC013 Unclassified Acute Myeloid Leukemia 7 1.095
136
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 13 1.090
137
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 10 1.090
138
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 10 1.090
139
SPL002 Splenic Manifestation of Prolymphocytic Leukemia 8 1.090
140
CLS019 Classic Mast Cell Leukemia 7 1.090
141
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 2 1.090
142
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 10 1.084
143
c ACT220 Acute Myeloid Leukemia, Kit-Related 7 1.084
144
c NPM001 Npm1-Related Acute Myeloid Leukemia 7 1.084
145
c ACT221 Acute Myeloid Leukemia, Somatic Dnmt3a-Related 6 1.084
146
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 4 1.084
147
WTL002 Wt Limb-Blood Syndrome 17 1.077
148
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 16 1.077
149
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 8 1.068
150
P LYM118 Lymphoma 69 0.478
151
BNM001 Bone Marrow Cancer 51 0.394
152
P LYM033 Lymphoproliferative Syndrome 56 0.391
153
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.375
154
LYM023 Lymphatic System Cancer 33 0.374
155
LYM024 Lymphatic System Disease 52 0.372
156
MRG013 Mirage Syndrome 29 0.370
157
MYL009 Myelodysplastic Syndrome 73 0.342
158
PRM243 Primary Bone Cancer 29 0.326
159
BNC003 Bone Cancer 58 0.300
160
MYL031 Myeloproliferative Neoplasm 58 0.285
161
c ADL001 Adult Lymphoma 39 0.272
162
HMT018 Hematopoietic Stem Cell Transplantation 41 0.269
163
LYM019 Lymphosarcoma 53 0.257
164
P BCL006 B-Cell Lymphomas 65 0.247
165
HMT002 Hematologic Cancer 64 0.245
166
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.241
167
c PRM023 Pre-Malignant Neoplasm 41 0.232
168
RFR004 Refractory Hematologic Cancer 28 0.227
169
BNL002 Bone Lymphoma 32 0.218
170
INC022 Inclusion-Cell Disease 46 0.214
171
PRP021 Peripheral Nervous System Neoplasm 46 0.209
172
BNS002 Bone Structure Disease 37 0.189
173
PRM151 Primary Bone Lymphoma 26 0.189
174
OCL009 Ocular Cancer 59 0.187
175
ADL002 Adult Syndrome 52 0.181
176
ACD009 Acid-Labile Subunit, Deficiency of 45 0.180
177
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.177
178
LYM115 Lymphoma, Non-Hodgkin 63 0.176
179
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.174
180
P CHR084 Chromosomal Disease 32 0.173
181
P NRV006 Nervous System Cancer 60 0.156
182
LKC003 Leukocyte Disease 43 0.156
183
ATN003 Autonomic Nervous System Neoplasm 40 0.153
184
P MLT019 Multiple Myeloma 83 0.153
185
SNS023 Sensory System Cancer 43 0.151
186
SRC014 Sarcoma 66 0.148
187
FRB001 Farber Lipogranulomatosis 53 0.146
188
P CNT005 Central Nervous System Lymphoma 53 0.146
189
PLS009 Plasma Cell Neoplasm 48 0.145
190
BND014 Bone Development Disease 40 0.145
191
ACR002 Acrocapitofemoral Dysplasia 33 0.145
192
P ACT135 Acute Graft Versus Host Disease 53 0.142
193
BRT030 Birth Defects 43 0.142
194
BLD053 Blood Platelet Disease 46 0.142
195
GST014 Gastrointestinal Lymphoma 31 0.141
196
RFR010 Refractory Anemia 45 0.140
197
c LYM106 Lymphoproliferative Syndrome 1 32 0.138
198
KDS001 Kid Syndrome 53 0.138
199
c LYM107 Lymphoproliferative Syndrome 2 50 0.138
200
CHL071 Child Syndrome 58 0.137
201
PDT001 Pediatric Lymphoma 38 0.134
202
GDS001 Good Syndrome 44 0.132
203
WLL006 Wells Syndrome 59 0.131
204
CSY001 C Syndrome 50 0.131
205
BRK010 Burkitt Lymphoma 69 0.129
206
c PRM226 Primary Central Nervous System Lymphoma 49 0.129
207
P NTR004 Neutropenia 59 0.128
208
HRT007 Heart Cancer 46 0.126
209
c CHR417 Chronic Graft Versus Host Disease 51 0.126
210
END072 Endotheliitis 42 0.126
211
P HRT017 Heart Tumor 32 0.125
212
DFC004 Deficiency Anemia 64 0.124
213
P MYL005 Myelofibrosis 67 0.123
214
DWN001 Down Syndrome 66 0.122
215
c ADL079 Adult Heart Tumor 16 0.120
216
ACR041 Acromelic Frontonasal Dysostosis 45 0.120
217
MNT001 Mantle Cell Lymphoma 72 0.119
218
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.118
219
HDG012 Hodgkin Lymphoma 77 0.117
220
HML018 Homologous Wasting Disease 13 0.115
221
P RFR008 Refractory Anemia with Excess Blasts 31 0.115
222
PRP036 Peripheral T-Cell Lymphoma 45 0.114
223
CNT010 Central Nervous System Hematologic Cancer 18 0.112
224
BLD054 Blood Protein Disease 37 0.110
225
DFF005 Diffuse Large B-Cell Lymphoma 59 0.108
226
IMM136 Immune System Disease 51 0.108
227
C3D001 C3 Deficiency 53 0.107
228
P FLL037 Follicular Lymphoma 70 0.106
229
ARG006 Aregenerative Anemia 22 0.106
230
P THR014 Thrombocytopenia 64 0.105
231
LYM127 Lymphatic Malformations 39 0.105
232
c CLL013 Cell Type Cancer 46 0.104
233
GLC077 Glucocorticoid Therapy, Response to 16 0.104
234
LYM126 Lymphoma Aids Related 15 0.104
235
RFR001 Refractory Plasma Cell Neoplasm 16 0.103
236
P HPT021 Hepatitis 69 0.103
237
P HML002 Hemolytic Anemia 62 0.102
238
ALN001 Aland Island Eye Disease 45 0.101
239
P MST009 Mastocytosis 56 0.100
240
P SPS003 Spastic Diplegia 52 0.100
241
MYL003 Myeloid Sarcoma 48 0.099
242
RTC009 Reticulum Cell Sarcoma 47 0.099
243
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.099
244
RDT005 Radiation Induced Cancer 28 0.098
245
RTC005 Reticulosarcoma 48 0.097
246
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.097
247
P HYP098 Hypereosinophilic Syndrome 63 0.097
248
VSC006 Vascular Cancer 51 0.097
249
MCR004 Macroglobulinemia 50 0.097
250
c RFR015 Refractory Anemia with Excess Blasts Type 1 15 0.097
251
P APL001 Aplastic Anemia 75 0.096
252
c RFR014 Refractory Anemia with Excess Blasts Type 2 16 0.096
253
P BRS047 Breast Cancer 100 0.096
254
LPD004 Lipoid Nephrosis 48 0.096
255
ATN002 Autonomic Nervous System Disease 48 0.096
256
MXD023 Mixed Cell Type Cancer 45 0.096
257
ALR002 Al-Raqad Syndrome 36 0.096
258
RFR007 Refractory Anemia with Excess Blasts in Transformation 20 0.096
259
ACT228 Acute Radiation Syndrome 20 0.096
260
GRN017 Granulocytopenia 44 0.094
261
ORL011 Oral Cancer 56 0.094
262
c FLL041 Follicular Lymphoma 1 45 0.094
263
c ATM010 Autoimmune Hemolytic Anemia 61 0.092
264
P BLD051 Blood Coagulation Disease 42 0.091
265
HRT029 Heart Tumor of the Child 15 0.091
266
P ORL007 Oral Cavity Cancer 59 0.090
267
THR024 Thrombosis 57 0.090
268
P HMR003 Hemorrhagic Disease 57 0.090
269
VSC008 Vascular Hemostatic Disease 30 0.090
270
HRT003 Heart Lymphoma 30 0.090
271
P ESS003 Essential Thrombocythemia 70 0.089
272
VND001 Vein Disease 47 0.089
273
c SYS004 Systemic Mastocytosis 60 0.088
274
CRD118 Cardiovascular Cancer 44 0.088
275
PCK002 Pick Disease 68 0.087
276
MRG003 Marginal Zone B-Cell Lymphoma 52 0.086
277
TCL019 T-Cell Childhood Lymphoblastic Lymphoma 14 0.086
278
P PLY018 Polycythemia 58 0.085
279
RCH001 Richter's Syndrome 45 0.084
280
GLC037 Glucocorticoid Resistance 62 0.084
281
PRD011 Proud Syndrome 42 0.084
282
P KDN017 Kidney Cancer 65 0.083
283
P HST010 Histiocytosis 58 0.082
284
LYM104 Lymphoma, Malt, Somatic 54 0.082
285
BNM005 Bone Marrow Necrosis 32 0.082
286
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.081
287
P ART022 Arthritis 75 0.081
288
P ASP006 Aspergillosis 61 0.081
289
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.081
290
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 39 0.081
291
P PNM007 Pneumonia 68 0.080
292
PRS047 Prostatitis 56 0.080
293
PRR002 Pure Red-Cell Aplasia 47 0.080
294
P WLD002 Waldenstrom Macroglobulinemia 58 0.079
295
LYM012 Lymphoplasmacytic Lymphoma 44 0.079
296
PLS025 Plasmablastic Lymphoma 46 0.076
297
WTH001 Withdrawal Disorder 37 0.076
298
NNH003 Non-Hodgkin Lymphoma, Childhood 12 0.076
299
P INF038 Influenza 72 0.075
300
c RTN162 Retinitis Pigmentosa 2 48 0.075
301
SPL012 Splenic Disease 46 0.075
302
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.075
303
SPL011 Spleen Cancer 36 0.075
304
P MNN013 Meningitis 67 0.075
305
WLM007 Wilms Tumor Susceptibility-5 63 0.075
306
P NRP001 Neuropathy 59 0.075
307
WST001 West Syndrome 57 0.075
308
SPL004 Splenic Marginal Zone Lymphoma 44 0.075
309
c MCR162 Macroglobulinemia, Waldenstrom 2 17 0.074
310
P NRF002 Neurofibromatosis 71 0.073
311
LKS001 Leukostasis 35 0.073
312
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.073
313
THR004 Thrombocytosis 55 0.072
314
TRP002 Tropical Spastic Paraparesis 55 0.072
315
SPS057 Spasticity 42 0.072
316
SPS019 Spastic Paraparesis 41 0.072
317
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 29 0.072
318
LYM048 Lymphoma, Large-Cell, Immunoblastic 25 0.072
319
c CRN173 Coronary Heart Disease 8 18 0.072
320
P HPT023 Hepatocellular Carcinoma 92 0.071
321
ISC004 Ischemia 61 0.071
322
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.071
323
P THY032 Thyroiditis 54 0.071
324
DSS009 Disseminated Intravascular Coagulation 51 0.071
325
RTN023 Retinitis 50 0.071
326
UTR033 Uterine Corpus Cancer 49 0.071
327
BCT015 Bacteremia 48 0.071
328
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.071
329
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.069
330
ADJ001 Adjustment Disorder 38 0.069
331
P RHM011 Rheumatoid Arthritis 89 0.068
332
P ATX030 Ataxia-Telangiectasia 77 0.068
333
MLN008 Melanoma 62 0.068
334
VSC011 Vasculitis 62 0.068
335
PRL032 Perlman Syndrome 50 0.068
336
CRB009 Cerebritis 39 0.068
337
DSS003 Disseminated Eosinophilic Collagen Disease 15 0.068
338
P ANP001 Anaplastic Large Cell Lymphoma 57 0.067
339
HYP266 Hypoxia 56 0.067
340
P PNC001 Pancytopenia 52 0.067
341
P CTN015 Cutaneous T Cell Lymphoma 50 0.067
342
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.067
343
SML025 Small Non-Cleaved Cell Lymphoma 22 0.067
344
SVR004 Severe Combined Immunodeficiency 69 0.066
345
c CHR096 Chronic Pulmonary Heart Disease 40 0.066
346
HDG004 Hodgkin's Granuloma 24 0.066
347
P PRS040 Prostate Cancer 90 0.065
348
LRN003 Learning Disability 49 0.065
349
c PRM149 Primary Hypereosinophilic Syndrome 38 0.065
350
c CRN177 Coronary Heart Disease 7 20 0.065
351
HDG006 Hodgkin's Paragranuloma 17 0.065
352
MYC006 Mycosis Fungoides 66 0.064
353
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.064
354
c SVR003 Severe Congenital Neutropenia 56 0.064
355
PST046 Post-Transplant Lymphoproliferative Disease 54 0.064
356
c TRC078 Trichohepatoenteric Syndrome 2 29 0.064
357
BNM011 Bone Marrow Failure Syndrome 2 25 0.064
358
c CRN214 Coronary Heart Disease 5 22 0.064
359
P RTN024 Retinoblastoma 74 0.063
360
P PNC044 Pancreatitis 61 0.063
361
P ATX004 Ataxia 53 0.063
362
SPL018 Splenomegaly 44 0.063
363
BRN028 Brain Cancer 70 0.063
364
DPH001 Diphtheria 59 0.063
365
PLS011 Plasmacytoma 56 0.063
366
c THR037 Thrombocytopenia 2 35 0.063
367
WSC001 Wisconsin Syndrome 14 0.063
368
RBR001 Roberts Syndrome 60 0.062
369
c INV001 Invasive Aspergillosis 47 0.062
370
P LNG032 Lung Cancer 95 0.061
371
P NRB001 Neuroblastoma 70 0.061
372
MCS002 Mucositis 55 0.061
373
TTR011 Tetraploidy 41 0.061
374
ENG004 Engraftment Syndrome 32 0.061
375
c CRN176 Coronary Heart Disease 9 18 0.061
376
WHT007 White Platelet Syndrome 15 0.061
377
P ADN016 Adenocarcinoma 69 0.060
378
PRP030 Purpura 58 0.060
379
NWC001 Newcastle Disease 54 0.060
380
ALL026 Allergic Hypersensitivity Disease 52 0.060
381
c MLG054 Malignant Histiocytosis 49 0.060
382
MDS022 Mediastinitis 41 0.060
383
LNG013 Lung Lymphoma 38 0.060
384
P ACT080 Acute Pulmonary Heart Disease 31 0.060
385
BNM010 Bone Marrow Failure Syndrome 1 29 0.060
386
c WLM005 Wilms Tumor 2 20 0.060
387
CHR066 Chronic Fatigue Syndrome 64 0.059
388
PLY125 Polycythemia Vera, Somatic 63 0.059
389
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.059
390
MTH009 Mouth Disease 61 0.059
391
c CNT035 Central Nervous System Disease 60 0.059
392
PRP019 Peripheral Nervous System Disease 55 0.059
393
c SML023 Small Cell Lung Cancer, Adult 15 0.059
394
PRP027 Peripheral Vascular Disease 69 0.058
395
P GLM007 Glomerulonephritis 59 0.058
396
BLS007 Blastic Plasmacytoid Dendritic Cell 41 0.058
397
LYM020 Lymph Node Cancer 39 0.058
398
P HRT032 Heart Disease 75 0.057
399
SCT005 Scott Syndrome 53 0.057
400
P DBT005 Diabetes Insipidus 53 0.057
401
P ACT105 Acute Mountain Sickness 52 0.057
402
LYM116 Lymph Node Disease 47 0.057
403
LYM051 Lymphomatoid Granulomatosis 47 0.057
404
c PRM225 Primary Thrombocytopenia 39 0.057
405
VSC001 Vascular Myelopathy 23 0.057
406
BNM013 Bone Marrow Failure Syndrome 3 17 0.057
407
AND005 Androgen Insensitivity Syndrome, Mild 16 0.057
408
P OBS005 Obesity 92 0.056
409
c HPT016 Hepatitis B 65 0.056
410
GNG013 Gingivitis 61 0.056
411
P INF032 Infertility 59 0.056
412
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.056
413
P TRC086 Trichohepatoenteric Syndrome 1 48 0.056
414
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 47 0.056
415
OST003 Osteonecrosis 45 0.056
416
FXF002 Fox-Fordyce Disease 36 0.056
417
IND005 Indolent B Cell Lymphoma 23 0.056
418
MND006 Mondor Disease 21 0.056
419
GST019 Gastrointestinal Stromal Tumor 73 0.054
420
ATR060 Atrial Standstill, Digenic 51 0.054
421
HMG002 Hemoglobinuria 48 0.054
422
ANG046 Angioimmunoblastic T-Cell Lymphoma 43 0.054
423
HV1006 Hiv-1 80 0.053
424
DRM006 Dermatitis 66 0.053
425
CNN005 Connective Tissue Disease 62 0.053
426
HPT074 Hepatic Adenoma, Somatic 50 0.053
427
MSC072 Muscle Cancer 49 0.053
428
P GRN010 Granular Cell Tumor 47 0.053
429
P CNN004 Connective Tissue Cancer 40 0.053
430
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.053
431
SPC003 Specific Developmental Disorder 38 0.053
432
YNG002 Young Syndrome 26 0.053
433
c ANP011 Anaplastic Small Cell Lymphoma 14 0.053
434
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.053
435
P HRP006 Herpes Simplex 65 0.052
436
P CND004 Candidiasis 57 0.052
437
MST017 Mast Cell Disease 50 0.052
438
P SKN013 Skin Benign Neoplasm 43 0.052
439
DND018 Dendritic Cell Tumor 41 0.052
440
c CNN010 Connective Tissue Benign Neoplasm 32 0.052
441
STT009 Sutton Disease 2 18 0.052
442
LYM041 Lymphocytes Absent 13 0.052
443
TBR010 Tuberculosis 70 0.051
444
c HPT001 Hepatitis C 68 0.051
445
CLT003 Colitis 60 0.051
446
RHB003 Rhabdomyosarcoma 57 0.051
447
c PRM012 Primary Polycythemia 52 0.051
448
TST015 Testicular Disease 44 0.051
449
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.051
450
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 34 0.051
451
c THR048 Thrombocytopenia 4 27 0.051
452
PRM133 Primary Pulmonary Lymphoma 23 0.051
453
P MYC007 Myocardial Infarction 79 0.050
454
EWN003 Ewing Sarcoma 66 0.050
455
CNT098 Central Core Disease 65 0.050
456
ADM013 Adamantinoma of Long Bones 57 0.050
457
SFT003 Soft Tissue Sarcoma 57 0.050
458
TST014 Testicular Cancer 53 0.050
459
CYT008 Cytomegalovirus Infection 52 0.050
460
MN1001 Mn1 30 0.050
461
CHR208 Chromosome 17p Deletion 20 0.050
462
c SCN042 Secondary Hypereosinophilic Syndrome 14 0.050
463
KDN020 Kidney Cancer, Childhood 11 0.050
464
P AMY004 Amyloidosis 65 0.049
465
HYP066 Hyperglycemia 61 0.049
466
P PLY019 Polyneuropathy 56 0.049
467
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.049
468
PRM025 Primary Bacterial Infectious Disease 41 0.049
469
NRN002 Neuronitis 41 0.049
470
HST016 Histiocytic Sarcoma 41 0.049
471
GST078 Gastrointestinal Allergy 40 0.049
472
HYP084 Hypopyon 31 0.049
473
MYL052 Myeloproliferative Neoplasms, Familial 15 0.049
474
NVD002 Nevada Syndrome 14 0.049
475
P RNL014 Renal Cell Carcinoma 82 0.047
476
P MDL005 Medulloblastoma 77 0.047
477
WLS001 Wilson Disease 72 0.047
478
P GLB002 Glioblastoma 68 0.047
479
c NRF018 Neurofibromatosis, Type 1 67 0.047
480
P NJM001 Nijmegen Breakage Syndrome 67 0.047
481
P ALX003 Alexander Disease 63 0.047
482
P GLM045 Glioma 60 0.047
483
PRC012 Pericardial Effusion 51 0.047
484
MLL012 Miller Syndrome 49 0.047
485
SKN023 Skin Tag 44 0.047
486
WRT001 Worth's Syndrome 34 0.047
487
CRB001 Cerebral Lymphoma 33 0.047
488
ZYG002 Zygomycosis 33 0.047
489
FSR001 Fusariosis 31 0.047
490
c THR110 Thrombocytopenia 6 20 0.047
491
HDG009 Hodgkin Lymphoma, Childhood 14 0.047
492
P CLR023 Colorectal Cancer 97 0.046
493
P NRV007 Nervous System Disease 71 0.046
494
TST021 Testicular Germ Cell Tumor 69 0.046
495
BRC012 Brucellosis 66 0.046
496
WLL001 Williams-Beuren Syndrome 60 0.046
497
P PRP029 Porphyria 59 0.046
498
P UVT001 Uveitis 58 0.046
499
PMP001 Pemphigus 50 0.046
500
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.046
501
P PLM006 Pulmonary Alveolar Proteinosis 48 0.046
502
HYP025 Hyperphosphatemia 47 0.046
503
TMP012 Temple Syndrome 38 0.046
504
FLL019 Follicular Mucinosis 25 0.046
505
c DLT001 Delta Chain Disease 13 0.046
506
c SYS001 Systemic Lupus Erythematosus 86 0.045
507
c HPT073 Hepatitis C Virus 73 0.045
508
SKN016 Skin Disease 66 0.045
509
c MNN043 Meningioma, Familial 59 0.045
510
LYM021 Lymphadenitis 58 0.045
511
c ACT027 Acute Pancreatitis 57 0.045
512
HRP004 Herpes Zoster 56 0.045
513
VRL011 Viral Infectious Disease 55 0.045
514
SZR001 Sezary's Disease 52 0.045
515
NTR040 Neutropenia, Cyclic 51 0.045
516
NSD001 Nose Disease 48 0.045
517
P SDR003 Sideroblastic Anemia 40 0.045
518
CMP001 Composite Lymphoma 37 0.045
519
ANP010 Anaplastic Plasmacytoma 19 0.045
520
ACC008 Accelerated Tumor Formation 17 0.045
521
CHR062 Chronic Erythremia 13 0.045
522
GST053 Gastric Cancer 78 0.044
523
P AST007 Astrocytoma 65 0.044
524
P LPS004 Lupus Erythematosus 64 0.044
525
P PRP003 Porphyria Cutanea Tarda 64 0.044
526
P HYP117 Hypertriglyceridemia 61 0.044
527
P GST049 Gastrointestinal System Cancer 60 0.044
528
P GT001 Gout 58 0.044
529
PRT011 Protein C Deficiency 52 0.044
530
MYC002 Mycobacterium Avium Complex Disease 52 0.044
531
BCK006 Back Pain 43 0.044
532
NTR018 Neutrophilia, Hereditary 42 0.044
533
PYM001 Pyomyositis 40 0.044
534
6MR001 6-Mercaptopurine Sensitivity 31 0.044
535
P RSP003 Respiratory Failure 71 0.042
536
SQM006 Squamous Cell Carcinoma 70 0.042
537
P ENC004 Encephalitis 63 0.042
538
MSL001 Measles 61 0.042
539
P END033 Endocarditis 54 0.042
540
TTH006 Tooth Disease 52 0.042
541
TXC002 Toxic Encephalopathy 51 0.042
542
PRP007 Priapism 46 0.042
543
P CRV039 Cervicitis 45 0.042
544
c JVN003 Juvenile Xanthogranuloma 44 0.042
545
MTR008 Mature B-Cell Neoplasm 40 0.042
546
PRN049 Paraneoplastic Pemphigus 40 0.042
547
SPN040 Spinal Cancer 39 0.042
548
SPN369 Spinal Disease 39 0.042
549
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.042
550
P CRN178 Coronary Heart Disease 6 21 0.042
551
c BNG076 Benign Exophthalmos Syndrome 15 0.042
552
P HNT016 Huntington Disease 80 0.041
553
P THY023 Thymoma 57 0.041
554
c THR092 Thrombophilia Due to Thrombin Defect 54 0.041
555
P LCT001 Lactic Acidosis 51 0.041
556
CLN015 Colon Adenocarcinoma 50 0.041
557
c ACT134 Acute Liver Failure 50 0.041
558
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.041
559
GRN007 Granuloma Annulare 37 0.041
560
LTH001 Lethal Midline Granuloma 37 0.041
561
CYC007 Cyclic Thrombocytopenia 37 0.041
562
ANG049 Angioedema Induced by Ace Inhibitors 34 0.041
563
c THR090 Thrombocythemia 1 30 0.041
564
c EYL003 Eye Lymphoma 30 0.041
565
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 26 0.041
566
c FML303 Familial/multiple Cancer 14 0.041
567
c ACT075 Acute Myocardial Infarction 60 0.039
568
P DRR001 Diarrhea 60 0.039
569
CHL067 Cholecystitis 57 0.039
570
URT039 Urticaria 57 0.039
571
P OLG002 Oligodendroglioma 56 0.039
572
MRK001 Merkel Cell Carcinoma 52 0.039
573
PYD001 Pyoderma Gangrenosum 51 0.039
574
CRS005 Crest Syndrome 51 0.039
575
INT253 Intestinal Benign Neoplasm 47 0.039
576
MMB001 Membranoproliferative Glomerulonephritis 46 0.039
577
CRY004 Cryoglobulinemia 46 0.039
578
AGG002 Aggressive Systemic Mastocytosis 42 0.039
579
P HVY001 Heavy Chain Disease 41 0.039
580
CNV002 Conversion Disorder 41 0.039
581
TST004 Testicular Lymphoma 37 0.039
582
NTR005 Nutritional Deficiency Disease 36 0.039
583
WDS002 Woods Syndrome 27 0.039
584
BRN049 Brain Tumor, Childhood 20 0.039
585
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 20 0.039
586
TTR021 Tetrasomy 21 20 0.039
587
ULC004 Ulcerative Colitis 76 0.038
588
THY028 Thyroid Cancer 69 0.038
589
PTR006 Peters Anomaly 65 0.038
590
GLB001 Gilbert Syndrome 60 0.038
591
P ENC018 Encephalopathy 59 0.038
592
ADN018 Adenoma 58 0.038
593
P MYS005 Myositis 57 0.038
594
RTN017 Retinal Detachment 56 0.038
595
P ANT006 Antiphospholipid Syndrome 56 0.038
596
P TRT010 Teratoma 52 0.038
597
PNN001 Panniculitis 51 0.038
598
STR008 Strongyloidiasis 51 0.038
599
FML037 Female Breast Cancer 50 0.038
600
KLN001 Klinefelter's Syndrome 50 0.038
601
CTN014 Cutaneous Mastocytosis 49 0.038
602
OBS001 Obstructive Jaundice 48 0.038
603
SCB001 Scabies 47 0.038
604
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.038
605
HYP017 Hypophosphatemia 43 0.038
606
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.038
607
ECT004 Ecthyma 35 0.038
608
PHY001 Physiological Polycythemia 28 0.038
609
LVR006 Liver Lymphoma 27 0.038
610
PRM128 Primary Cutaneous Follicle Center Lymphoma 26 0.038
611
HNM002 Hinman Syndrome 25 0.038
612
CNT067 Central Cord Syndrome 23 0.038
613
NVS004 Nova Syndrome 13 0.038
614
MNT045 Montefiore Syndrome 10 0.038
615
P OVR042 Ovarian Cancer 76 0.036
616
INS024 Insulin-Like Growth Factor I 75 0.036
617
CNG034 Congestive Heart Failure 72 0.036
618
ATP002 Atopy 66 0.036
619
P CNJ013 Conjunctivitis 64 0.036
620
OST017 Osteomyelitis 61 0.036
621
P SNS014 Sinusitis 60 0.036
622
APP008 Appendicitis 60 0.036
623
P NPH012 Nephrotic Syndrome 59 0.036
624
BRN012 Bronchiolitis Obliterans 58 0.036
625
P EXN002 Exanthem 57 0.036
626
TNS005 Tonsillitis 57 0.036
627
BRN002 Bronchiolitis 56 0.036
628
P LPS002 Liposarcoma 55 0.036
629
P PLY041 Polymyositis 52 0.036
630
CLL003 Cellulitis 51 0.036
631
GRW007 Growth Hormone Deficiency 50 0.036
632
STM007 Stomatitis 50 0.036
633
P FNC004 Fanconi Syndrome 49 0.036
634
P SCL015 Scleritis 49 0.036
635
TCL003 T Cell Deficiency 45 0.036
636
CRD001 Cardiac Tamponade 44 0.036
637
MST004 Mast Cell Neoplasm 40 0.036
638
RDN001 Reading Disorder 34 0.036
639
CYT004 Cytomegalic Inclusion Disease 31 0.036
640
GRN016 Grant Syndrome 29 0.036
641
TRS012 Trisomy 22 27 0.036
642
c THR102 Thrombocytopenia 5 27 0.036
643
c ALX006 Alexander Disease Type Ii 15 0.036
644
c ALX007 Alexander Disease Type I 15 0.036
645
P LVR013 Liver Disease 75 0.034
646
P AGM001 Agammaglobulinemia 64 0.034
647
P ART023 Arthropathy 64 0.034
648
OST085 Osteosarcoma, Somatic 63 0.034
649
P ALP009 Alopecia Areata 62 0.034
650
SPT004 Septic Arthritis 60 0.034
651
CRN036 Craniopharyngioma 59 0.034
652
ALP008 Alopecia 57 0.034
653
GLL022 Guillain-Barre Syndrome 56 0.034
654
OLV001 Olivopontocerebellar Atrophy 53 0.034
655
P HML001 Hemolytic-Uremic Syndrome 51 0.034
656
HYP005 Hypokalemia 51 0.034
657
SPN041 Spinal Cord Disease 51 0.034
658
MGL001 Megaloblastic Anemia 50 0.034
659
P INT063 Intellectual Disability 49 0.034
660
PYD002 Pyoderma 48 0.034
661
CYT005 Cytomegalovirus Retinitis 47 0.034
662
THY009 Thyroid Lymphoma 47 0.034
663
INT054 Intraocular Lymphoma 45 0.034
664
MLL018 Miller-Dieker Lissencephaly Syndrome 45 0.034
665
PRN011 Pernicious Anemia 44 0.034
666
ANG037 Angiomatosis 37 0.034
667
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.034
668
CRB040 Cerebrum Cancer 32 0.034
669
BRS001 Breast Lymphoma 32 0.034
670
SPR035 Superior Vena Cava Syndrome 31 0.034
671
RCM004 Recombinant 8 Syndrome 22 0.034
672
GNR023 Generalized Eruptive Histiocytosis 20 0.034
673
BNM008 Bone Mineral Density, Low 16 0.034
674
TST022 Testicular Cancer, Childhood 11 0.034
675
P PLM037 Pulmonary Hypertension 79 0.033
676
P MYP004 Myopathy 67 0.033
677
BLM001 Bloom Syndrome 63 0.033
678
HYP056 Hypoglycemia 61 0.033
679
P PSR002 Psoriasis 61 0.033
680
P ESP024 Esophagitis 61 0.033
681
ETN001 Eating Disorder 58 0.033
682
EXF001 Exfoliation Syndrome 57 0.033
683
P SML001 Small Cell Carcinoma 56 0.033
684
LYM027 Lymphopenia 56 0.033
685
P AVS004 Avascular Necrosis of the Femoral Head 56 0.033
686
HPT022 Hepatoblastoma 55 0.033
687
RCT018 Rectal Neoplasm 54 0.033
688
PLN006 Poland Syndrome 54 0.033
689
P SML016 Small Intestine Cancer 52 0.033
690
PPL002 Papillary Carcinoma 51 0.033
691
CLC006 Calcinosis 50 0.033
692
PRP016 Paraplegia 49 0.033
693
CMR002 Coumarin Resistance 48 0.033
694
HYP063 Hypersplenism 48 0.033
695
P CMP008 Compartment Syndrome 48 0.033
696
FLL008 Folliculitis 46 0.033
697
c MLG081 Malignant Teratoma 46 0.033
698
P PLN008 Peeling Skin Syndrome 45 0.033
699
MST006 Mast Syndrome 43 0.033
700
PRT026 Parotitis 42 0.033
701
NRW001 Norwegian Scabies 42 0.033
702
ANP009 Anaplastic Oligodendroglioma 41 0.033
703
LYM052 Lymphomatoid Papulosis 41 0.033
704
c CNG031 Congenital Nervous System Abnormality 37 0.033
705
URT008 Urticaria Pigmentosa 37 0.033
706
CRB026 Cerebellar Astrocytoma 37 0.033
707
EMN001 Emanuel Syndrome 36 0.033
708
ACL001 Acalculous Cholecystitis 35 0.033
709
SPL006 Splenic Infarction 35 0.033
710
SGT001 Sagittal Sinus Thrombosis 35 0.033
711
MXD032 Mixed Germ Cell Tumor 34 0.033
712
MNC004 Monoclonal Paraproteinemia 34 0.033
713
EPG003 Epiglottitis 33 0.033
714
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.033
715
DFF027 Diffuse Lymphatic Malformation 22 0.033
716
ATX038 Ataxia and Polyneuropathy, Adult-Onset 21 0.033
717
c WLM011 Wilms Tumor 6 19 0.033
718
c TCL008 T-Cell Lymphoma 1a 17 0.033
719
P AST005 Asthma 82 0.031
720
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.031
721
P HMC003 Hemochromatosis 72 0.031
722
c FNC027 Fanconi Anemia, Complementation Group a 71 0.031
723
SCK003 Sickle Cell Anemia 71 0.031
724
ANX002 Anxiety Disorder 67 0.031
725
KPS004 Kaposi Sarcoma 67 0.031
726
P MYS003 Myasthenia Gravis 67 0.031
727
LSH001 Leishmaniasis 66 0.031
728
INC002 Inclusion Body Myositis 66 0.031
729
P OST002 Osteoporosis 64 0.031
730
MXD005 Mixed Connective Tissue Disease 62 0.031
731
CRD119 Cardiac Arrest 61 0.031
732
SHW002 Shwachman-Diamond Syndrome 61 0.031
733
P THR015 Thrombophilia 59 0.031
734
P HMP007 Hemophilia 57 0.031
735
EMB004 Embryonal Carcinoma 57 0.031
736
MYX005 Myxoid Liposarcoma 57 0.031
737
ANR040 Aneurysm 57 0.031
738
VSC003 Visceral Leishmaniasis 56 0.031
739
ERY003 Erythema Multiforme 55 0.031
740
P LRY019 Laryngitis 54 0.031
741
SML033 Small Cell Cancer of the Lung, Somatic 54 0.031
742
RSC001 Rosacea 52 0.031
743
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.031
744
PRC013 Pericarditis 51 0.031
745
MYL001 Myelitis 51 0.031
746
P HYP014 Hyperuricemia 50 0.031
747
INT007 Intermediate Coronary Syndrome 50 0.031
748
c ALM001 Al Amyloidosis 49 0.031
749
CNG028 Congenital Hypoplastic Anemia 48 0.031
750
PPL021 Papilledema 47 0.031
751
P CRN035 Cranial Nerve Palsy 46 0.031
752
MYL013 Myeloperoxidase Deficiency 46 0.031
753
INT067 Interstitial Nephritis 46 0.031
754
VSC047 Vascular Malformation 45 0.031
755
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.031
756
CLD007 Cold Agglutinin Disease 44 0.031
757
NCR004 Nocardiosis 43 0.031
758
P CPL003 Capillary Leak Syndrome 41 0.031
759
SML008 Small Intestine Lymphoma 40 0.031
760
c PLN018 Peeling Skin Syndrome 2 40 0.031
761
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.031
762
PRL008 Paralytic Ileus 37 0.031
763
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.031
764
GRM001 Germ Cell and Embryonal Cancer 36 0.031
765
MDS018 Mediastinal Cancer 36 0.031
766
CHP002 Chops Syndrome 35 0.031
767
MDS019 Mediastinal Malignant Lymphoma 33 0.031
768
LYM045 Lymphocytic Vasculitis 33 0.031
769
LNS003 Lens Disease 33 0.031
770
GLB003 Globe Disease 32 0.031
771
PRN039 Paraneoplastic Syndromes 32 0.031
772
SPL007 Splenic Abscess 30 0.031
773
c PLN021 Peeling Skin Syndrome 3 29 0.031
774
PNM003 Pneumatosis Cystoides Intestinalis 29 0.031
775
SPN026 Spinal Cord Lymphoma 24 0.031
776
CLR062 Colorblindness, Protan 24 0.031
777
c RNG017 Ring Chromosome 21 23 0.031
778
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.031
779
c RNL016 Renal Infectious Disease 20 0.031
780
P WSK001 Wiskott-Aldrich Syndrome 73 0.029
781
P DMN001 Diamond-Blackfan Anemia 69 0.029
782
CMM004 Common Variable Immunodeficiency 68 0.029
783
WRN001 Werner Syndrome 67 0.029
784
P THL005 Thalassemia 64 0.029
785
P HYP086 Hypothyroidism 64 0.029
786
GLB015 Glioblastoma Multiforme 63 0.029
787
P ADD001 Addison's Disease 62 0.029
788
P LYM025 Lymphedema 61 0.029
789
P FCL005 Focal Segmental Glomerulosclerosis 60 0.029
790
P PRT013 Portal Hypertension 60 0.029
791
c ATM011 Autoimmune Hepatitis 60 0.029
792
P RHN004 Rhinitis 60 0.029
793
c HPT003 Hepatitis a 59 0.029
794
P GRV001 Graves' Disease 59 0.029
795
BLL006 Bullous Pemphigoid 59 0.029
796
PYR013 Pyruvate Kinase Deficiency 58 0.029
797
P MMP001 Mumps 58 0.029
798
ABL002 Ablepharon-Macrostomia Syndrome 57 0.029
799
c FML108 Familial Breast Cancer 57 0.029
800
P RBL001 Rubella 57 0.029
801
P BCK002 Beckwith-Wiedemann Syndrome 56 0.029
802
NRN004 Neuroendocrine Tumor 56 0.029
803
P LMY004 Leiomyosarcoma 55 0.029
804
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.029
805
P FND001 Fundus Albipunctatus 55 0.029
806
PLM012 Pulmonary Sarcoidosis 54 0.029
807
HDC001 Headache 54 0.029
808
c HPT007 Hepatitis E 54 0.029
809
SLP005 Sleep Disorder 53 0.029
810
P EPN002 Ependymoma 53 0.029
811
HST011 Histoplasmosis 52 0.029
812
CRH005 Crohn's Colitis 52 0.029
813
PHL006 Phelan-Mcdermid Syndrome 51 0.029
814
c ADL023 Adult Medulloblastoma 51 0.029
815
GRD007 Grade Iii Astrocytoma 50 0.029
816
BNF002 Bone Fracture 50 0.029
817
EPD001 Epidermodysplasia Verruciformis 50 0.029
818
PLR008 Pleurisy 50 0.029
819
END035 Endocrine Gland Cancer 49 0.029
820
END021 Endomyocardial Fibrosis 49 0.029
821
GLM004 Gliomatosis Cerebri 49 0.029
822
MCP006 Mucoepidermoid Carcinoma 48 0.029
823
ECT026 Ectopic Pregnancy 48 0.029
824
RPP001 Rapp-Hodgkin Syndrome 48 0.029
825
ORL005 Oral Candidiasis 48 0.029
826
GYN001 Gynecomastia 48 0.029
827
DWR001 Dwarfism 47 0.029
828
PLY020 Polyradiculoneuropathy 45 0.029
829
P END047 Endophthalmitis 45 0.029
830
CHR008 Choroiditis 44 0.029
831
RTN001 Retinal Vasculitis 44 0.029
832
RGH009 Right Atrial Isomerism 44 0.029
833
P DMY001 Demyelinating Polyneuropathy 43 0.029
834
HYP299 Hyperostosis, Endosteal 43 0.029
835
PHY002 Physical Disorder 43 0.029
836
FBR003 Fibrous Histiocytoma 43 0.029
837
EWN002 Ewing's Family of Tumors 43 0.029
838
c ACQ014 Acquired Hemophilia 42 0.029
839
DDN006 Duodenitis 42 0.029
840
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.029
841
MYC017 Mycobacterium Kansasii 40 0.029
842
EPS006 Epstein Syndrome 39 0.029
843
SCR001 Secretory Meningioma 38 0.029
844
CRB036 Cerebral Meningioma 36 0.029
845
VRS001 Virus Associated Hemophagocytic Syndrome 35 0.029
846
SPN060 Spondylocarpotarsal Synostosis Syndrome 34 0.029
847
MLR007 Male Reproductive System Disease 34 0.029
848
c SRC023 Sarcoidosis 2 33 0.029
849
PLY119 Polymicrogyria, Bilateral Perisylvian 30 0.029
850
c NRB015 Neuroblastoma 2 28 0.029
851
c NRB014 Neuroblastoma 3 28 0.029
852
c THR086 Thrombocythemia 3 25 0.029
853
P SML002 Small Cell Sarcoma 25 0.029
854
ATM052 Autoimmune Disease 1 25 0.029
855
BCL011 Bacillary Angiomatosis 24 0.029
856
MCD002 Mcdonough Syndrome 23 0.029
857
c CRN175 Coronary Heart Disease 4 19 0.029
858
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 18 0.029
859
ATM053 Autoimmune Disease 2 16 0.029
860
BRN069 Brain and Spinal Tumors 12 0.029
861
SFT004 Soft Tissue Sarcoma Childhood 12 0.029
862
MLR004 Malaria 83 0.027
863
P RTT002 Rett Syndrome 77 0.027
864
CRH001 Crohn's Disease 75 0.027
865
P CRD011 Cardiomyopathy 68 0.027
866
P EPL164 Epilepsy 66 0.027
867
ACR007 Acromegaly 66 0.027
868
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.027
869
CHR012 Chronic Granulomatous Disease 65 0.027
870
P MSC005 Muscular Dystrophy 65 0.027
871
c BSL007 Basal Cell Carcinoma 65 0.027
872
CHD001 Chediak-Higashi Syndrome 64 0.027
873
P FML161 Familial Mediterranean Fever, Ar 63 0.027
874
P GCH001 Gaucher's Disease 62 0.027
875
TTN003 Tetanus 61 0.027
876
P TMP003 Temporal Arteritis 60 0.027
877
ACQ007 Acquired Immunodeficiency Syndrome 60 0.027
878
PRM097 Primary Immunodeficiency Disease 60 0.027
879
QFV001 Q Fever 60 0.027
880
GST045 Gastroenteritis 59 0.027
881
RSP006 Respiratory System Disease 58 0.027
882
P INT070 Intestinal Obstruction 57 0.027
883
P SZR006 Seizure Disorder 56 0.027
884
P BDD001 Budd-Chiari Syndrome 56 0.027
885
LTT002 Letterer-Siwe Disease 56 0.027
886
P FNC043 Fanconi Anemia, Complementation Group E 55 0.027
887
P HYP076 Hyperthyroidism 55 0.027
888
END030 End Stage Renal Failure 55 0.027
889
FLR002 Filariasis 54 0.027
890
PLM010 Pulmonary Edema 54 0.027
891
LST001 Listeriosis 53 0.027
892
P HYP024 Hypoparathyroidism 53 0.027
893
WHM001 Whim Syndrome 53 0.027
894
THR016 Thrombophlebitis 53 0.027
895
MNT002 Mental Depression 53 0.027
896
ERD001 Erdheim-Chester Disease 52 0.027
897
BRN106 Burns 52 0.027
898
NRT004 Neuritis 52 0.027
899
ATY005 Atypical Teratoid Rhabdoid Tumor 52 0.027
900
BRN038 Bronchial Disease 51 0.027
901
P PTS002 Ptosis 51 0.027
902
ASP003 Aseptic Meningitis 51 0.027
903
HNT002 Hantavirus Pulmonary Syndrome 51 0.027
904
CCC002 Coccidiosis 51 0.027
905
INF034 Infective Endocarditis 51 0.027
906
P PNV001 Panuveitis 50 0.027
907
EXT010 Extramedullary Plasmacytoma 49 0.027
908
PRT038 Protein-Energy Malnutrition 49 0.027
909
c INH020 Inherited Metabolic Disorder 49 0.027
910
BCL002 B Cell Deficiency 49 0.027
911
QBC001 Quebec Platelet Disorder 48 0.027
912
PST062 Pustulosis Palmaris Et Plantaris 48 0.027
913
CRN017 Coronary Thrombosis 48 0.027
914
FSC004 Fasciitis 48 0.027
915
HST009 Histiocytoma 47 0.027
916
HYD002 Hydronephrosis 47 0.027
917
GNG002 Ganglioneuroma 47 0.027
918
CHL018 Childhood Medulloblastoma 47 0.027
919
HMS001 Hemosiderosis 46 0.027
920
c GMM003 Gamma Heavy Chain Disease 46 0.027
921
HMN032 Human Herpesvirus 8 46 0.027
922
HPT014 Hepatorenal Syndrome 46 0.027
923
CHR074 Choriocarcinoma 46 0.027
924
IDP064 Idiopathic Neutropenia 45 0.027
925
ANR004 Anuria 45 0.027
926
BRN014 Bronchopneumonia 45 0.027
927
PTT037 Pituitary Tumors 45 0.027
928
P MTH007 Methemoglobinemia 45 0.027
929
HDR003 Hidradenitis 45 0.027
930
P SDR002 Siderosis 44 0.027
931
HYP085 Hypothalamic Disease 44 0.027
932
PLM039 Pulmonary Neuroendocrine Tumor 42 0.027
933
MCR017 Macrocytic Anemia 42 0.027
934
IMM001 Immune-Complex Glomerulonephritis 42 0.027
935
CRB002 Cerebral Primitive Neuroectodermal Tumor 41 0.027
936
AYM001 Ayme-Gripp Syndrome 41 0.027
937
RPR002 Reproductive System Disease 41 0.027
938
CNT025 Central Pontine Myelinolysis 41 0.027
939
CDQ001 Cauda Equina Syndrome 41 0.027
940
MLR002 Miliary Tuberculosis 41 0.027
941
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.027
942
ACT084 Acute Stress Disorder 40 0.027
943
RCT017 Rectal Disease 40 0.027
944
TRP014 Triploidy 40 0.027
945
PRV003 Perivascular Epithelioid Cell Tumor 39 0.027
946
THR035 Thrombasthenia 39 0.027
947
c CHR091 Chronic Meningitis 39 0.027
948
P RTN022 Retinal Vein Occlusion 38 0.027
949
LNG004 Langerhans Cell Sarcoma 37 0.027
950
PRM026 Primary Systemic Mycosis 37 0.027
951
P WGN003 Wagner Syndrome 36 0.027
952
c HRD009 Hereditary Wilms' Tumor 36 0.027
953
c CNT016 Central Retinal Vein Occlusion 36 0.027
954
P SPR013 Spiradenoma 36 0.027
955
MLG041 Malignant Triton Tumor 36 0.027
956
PHT003 Phototoxic Dermatitis 35 0.027
957
CRB030 Cerebellum Cancer 35 0.027
958
ADP007 Adie Pupil 34 0.027
959
c PLN017 Peeling Skin Syndrome 1 34 0.027
960
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.027
961
PLY010 Polyclonal Hypergammaglobulinemia 32 0.027
962
GNG006 Gingival Hypertrophy 32 0.027
963
c CTR122 Cataract 5, Multiple Types 32 0.027
964
P BRN030 Brain Ependymoma 32 0.027
965
CRB028 Cerebellar Medulloblastoma 31 0.027
966
PDT014 Pediatric Ependymoma 31 0.027
967
KDN019 Kidney Sarcoma 31 0.027
968
P ATX010 Ataxia Neuropathy Spectrum 30 0.027
969
BRW006 Brown Syndrome 29 0.027
970
VSL005 Visual Pathway Disease 29 0.027
971
c WGN005 Wagner Syndrome 1 28 0.027
972
ISL010 Isolated 17-Linked Lissencephaly 28 0.027
973
P EPS030 Episodic Kinesigenic Dyskinesia 1 27 0.027
974
EXF003 Exfoliative Dermatitis 25 0.027
975
CLL010 Cellular Ependymoma 24 0.027
976
MLN012 Melanoma and Neural System Tumor Syndrome 24 0.027
977
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.027
978
NNN007 Non-Involuting Congenital Hemangioma 19 0.027
979
PDT020 Pediatric Germ Cell Cancer 17 0.027
980
CNT045 Central Nervous System Sarcoma 16 0.027
981
ALL025 Allopurinol Toxicity 15 0.027
982
SYS059 Systemic Mastocytosis with an Associated Clonal Hematologic Non-Mast Cell Lineage Disease 13 0.027
983
c SLC031 Slco1b1-Related Altered Drug Metabolism 10 0.027
984
P PNC035 Pancreatic Cancer 87 0.024
985
DCH001 Duchenne Muscular Dystrophy 79 0.024
986
P SCH015 Schizophrenia 77 0.024
987
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.024
988
KRT004 Keratitis 71 0.024
989
P CLC005 Celiac Disease 68 0.024
990
LVR012 Liver Cirrhosis 67 0.024
991
P PLR004 Pleuropulmonary Blastoma 65 0.024
992
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.024
993
P LNG028 Long Qt Syndrome 64 0.024
994
P RBN001 Rubinstein-Taybi Syndrome 64 0.024
995
P INF037 Inflammatory Bowel Disease 63 0.024
996
P DYS007 Dyskeratosis Congenita 63 0.024
997
ALL003 Allergic Rhinitis 63 0.024
998
RNL101 Renal Cell Carcinoma, Papillary 63 0.024
999
PRT036 Peritonitis 63 0.024
1000
P CNT061 Conotruncal Heart Malformations 62 0.024
1001
P DRM010 Dermatomyositis 62 0.024
1002
ACN011 Acne 62 0.024
1003
FCT003 Factor X Deficiency 61 0.024
1004
P TXP001 Toxoplasmosis 61 0.024
1005
P ADL010 Adult Respiratory Distress Syndrome 61 0.024
1006
c VRL010 Viral Hepatitis 60 0.024
1007
P CTR002 Cataract 58 0.024
1008
P BRS044 Breast Adenocarcinoma 58 0.024
1009
PTT006 Pituitary Adenoma 56 0.024
1010
END041 Endometrial Adenocarcinoma 56 0.024
1011
P FBR017 Fibrosarcoma 56 0.024
1012
GST023 Gastric Ulcer 56 0.024
1013
P HMR012 Hemorrhagic Fever 56 0.024
1014
P WVR001 Weaver Syndrome 56 0.024
1015
PRR007 Perry Syndrome 55 0.024
1016
P TMT001 Timothy Syndrome 55 0.024
1017
VGT001 Vogt-Koyanagi-Harada Disease 55 0.024
1018
APH002 Aphasia 54 0.024
1019
LMY002 Leiomyoma 54 0.024
1020
P MTC069 Mitochondrial Disorders 53 0.024
1021
GST027 Gastric Lymphoma 53 0.024
1022
FDL002 Food Allergy 53 0.024
1023
PRT014 Protein S Deficiency 53 0.024
1024
GNT003 Genital Herpes 53 0.024
1025
P LTR001 Lateral Sclerosis 53 0.024
1026
P CYS018 Cystitis 52 0.024
1027
DSS008 Disease of Mental Health 52 0.024
1028
KRT002 Keratomalacia 52 0.024
1029
P ICH004 Ichthyosis 52 0.024
1030
GST040 Gastric Adenocarcinoma 52 0.024
1031
OCL022 Ocular Melanoma 52 0.024
1032
CHC001 Chickenpox 51 0.024
1033
P DRM007 Dermatitis Herpetiformis 51 0.024
1034
KMR001 Kimura Disease 50 0.024
1035
FML038 Female Reproductive Organ Cancer 50 0.024
1036
RDC002 Radiculopathy 50 0.024
1037
P CHR345 Chronic Pain 50 0.024
1038
RHB001 Rhabdoid Cancer 50 0.024
1039
LPR001 Lepromatous Leprosy 50 0.024
1040
INT075 Intracranial Hypertension 50 0.024
1041
HLL004 Hellp Syndrome 50 0.024
1042
HYP037 Hyperhomocysteinemia 50 0.024
1043
ERY017 Erythema Elevatum Diutinum 49 0.024
1044
c ACT071 Acute Kidney Failure 49 0.024
1045
c INF067 Inflammatory Bowel Disease 10 49 0.024
1046
SLD003 Sialadenitis 49 0.024
1047
GSG001 Gas Gangrene 49 0.024
1048
PRT018 Portal Vein Thrombosis 49 0.024
1049
LMB002 Lambert-Eaton Myasthenic Syndrome 49 0.024
1050
ACT017 Acute Chest Syndrome 48 0.024
1051
MSS002 Mass Syndrome 48 0.024
1052
THY030 Thyroid Gland Disease 48 0.024
1053
BRN032 Brain Glioma 48 0.024
1054
P OTT001 Otitis Externa 47 0.024
1055
P PTT014 Pitt-Hopkins Syndrome