Search results for "leukemia"

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

4023 hits were found for 'leukemia'

# Family MCID Name MIFTS Score
1
P MYL006 Myeloid Leukemia 59 7.026
2
c LKM062 Leukemia, Acute Lymphoblastic 63 6.632
3
c LKM061 Leukemia, Acute Myeloid 74 6.595
4
c CHR090 Chronic Lymphocytic Leukemia 70 6.531
5
P LKM002 Leukemia 61 6.323
6
P LKM068 Leukemia, Chronic Myeloid, Somatic 62 5.882
7
LKM067 Leukemia, Acute Promyelocytic, Somatic 49 4.901
8
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 53 4.679
9
MGK001 Megakaryocytic Leukemia 47 4.347
10
c ACT009 Acute Monocytic Leukemia 43 4.275
11
c ACT073 Acute Leukemia 49 4.213
12
c ACT020 Acute T Cell Leukemia 35 4.052
13
P LYM026 Lymphoblastic Leukemia 57 3.770
14
HCL001 Hcl-V 52 3.699
15
c ADL017 Adult T-Cell Leukemia 48 3.695
16
NTR003 Natural Killer Cell Leukemia 38 3.611
17
ACT216 Acute Leukemia of Ambiguous Lineage 27 3.541
18
P ACT074 Acute Lymphocytic Leukemia 48 3.396
19
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 39 3.393
20
CHR285 Chronic Myelomonocytic Leukemia 44 3.390
21
P TCL004 T-Cell Leukemia 40 3.319
22
ACT098 Acute Erythroid Leukemia 41 3.317
23
c ADL052 Adult Acute Lymphocytic Leukemia 36 3.202
24
ACT103 Acute Lymphoblastic Leukemia, Childhood 29 3.191
25
P MNC007 Monocytic Leukemia 45 3.157
26
ACT095 Acute Biphenotypic Leukemia 30 3.045
27
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 17 2.976
28
c SBC004 Subacute Myeloid Leukemia 29 2.974
29
P PRC048 Precursor B-Cell Acute Lymphoblastic Leukemia 44 2.939
30
c CHR064 Chronic Monocytic Leukemia 30 2.937
31
ACT114 Acute Myeloblastic Leukemia Without Maturation 24 2.929
32
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 11 2.885
33
c CHR418 Chronic Leukemia 34 2.885
34
c PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 35 2.867
35
TCL002 T-Cell Large Granular Lymphocyte Leukemia 36 2.826
36
PRL017 Prolymphocytic Leukemia 38 2.813
37
MST002 Mast-Cell Leukemia 39 2.798
38
CHL061 Childhood Leukemia 40 2.790
39
LRG008 Large Granular Lymphocyte Leukemia 30 2.717
40
ACT113 Acute Myeloblastic Leukemia with Maturation 28 2.703
41
ACT200 Acute Monoblastic Leukemia 35 2.694
42
c LKM005 Leukemia, T-Cell, Chronic 18 2.669
43
LYM067 Lymphoid Leukemia 36 2.644
44
PLS016 Plasma Cell Leukemia 30 2.579
45
CNT018 Central Nervous System Leukemia 28 2.534
46
CHR286 Chronic Neutrophilic Leukemia 38 2.369
47
c LKM004 Leukemia, B-Cell, Chronic 18 2.360
48
c LKM055 Leukemia, Acute Lymphoblastic 2 10 2.348
49
c LKM056 Leukemia, Chronic Lymphocytic 2 13 2.332
50
ACT118 Acute Non Lymphoblastic Leukemia 28 2.322
51
c LKM050 Leukemia, Chronic Lymphocytic 1 10 2.316
52
c LKM051 Leukemia, Chronic Lymphocytic 3 11 2.232
53
NNN022 Noonan Syndrome-Like Disorder with or Without Juvenile Myelomonocytic Leukemia 31 2.196
54
SBL003 Subleukemic Leukemia 11 2.193
55
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 15 2.189
56
c TCL005 T-Cell Prolymphocytic Leukemia 40 2.117
57
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 14 2.104
58
P BCL005 B Cell Prolymphocytic Leukemia 35 2.066
59
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 28 2.047
60
PLS003 Plasmacytic Leukemia 15 1.999
61
FML045 Familial Mosaic Monosomy 7 Syndrome 17 1.993
62
P LFR001 Li-Fraumeni Syndrome 79 1.991
63
TST003 Testicular Leukemia 23 1.977
64
c LKM060 Leukemia, Acute Lymphoblastic 3 11 1.934
65
NLL001 Null-Cell Leukemia 18 1.900
66
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 9 1.832
67
CLL014 Cll/sll 31 1.823
68
ACT177 Acute Basophilic Leukemia 28 1.713
69
c ACT219 Acute Myeloid Leukemia, Flt3-Related 23 1.698
70
CRB138 Core Binding Factor Acute Myeloid Leukemia 34 1.686
71
LYM040 Lymphoblastic Lymphoma 48 1.663
72
ALK003 Aleukemic Leukemia Cutis 30 1.653
73
RFR002 Refractory Hairy Cell Leukemia 21 1.645
74
BND002 B- and T-Cell Mixed Leukemia 9 1.626
75
P CHR562 Chronic Myelocytic Leukemia 30 1.625
76
PDT026 Pediatric T-Cell Leukemia 4 1.621
77
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 13 1.606
78
BLS007 Blastic Plasmacytoid Dendritic Cell 37 1.605
79
AML051 Aml with Myelodysplasia-Related Features 13 1.605
80
NNT007 Neonatal Leukemia 26 1.601
81
ACT222 Acute Pre-B-Cell Lymphoblastic Leukemia 12 1.585
82
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 15 1.583
83
P 8P1002 8p11 Myeloproliferative Syndrome 35 1.572
84
c SBC006 Subacute Leukemia 11 1.572
85
HRY001 Hairy Cell Leukemia of Spleen 9 1.569
86
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 26 1.563
87
ALK002 Aleukemic Monocytic Leukemia Cutis 10 1.560
88
SQM013 Squamous Cell Carcinoma, Head and Neck 71 1.556
89
c SBC015 Subacute Monocytic Leukemia 12 1.556
90
SPL013 Splenic Manifestation of Leukemia 10 1.556
91
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 4 1.556
92
c INH015 Inherited Acute Myeloid Leukemia 14 1.553
93
ACT196 Acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2) 9 1.549
94
NNN023 Noonan Syndrome-Like Disorder with Juvenile Myelomonocytic Leukemia 8 1.544
95
CHL029 Childhood Precursor T-Lymphoblastic Lymphoma/leukemia 6 1.544
96
SPL002 Splenic Manifestation of Prolymphocytic Leukemia 4 1.544
97
SPL010 Splenic Manifestation of Hairy Cell Leukemia 4 1.544
98
PRG005 Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 6 1.540
99
PST004 Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 6 1.540
100
c HMN021 Human T-Cell Leukemia Virus Type 1 42 1.513
101
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 9 1.315
102
CHR563 Chronic Eosinophilic Leukemia 36 1.309
103
P HYP098 Hypereosinophilic Syndrome 49 1.254
104
c SYS004 Systemic Mastocytosis 56 1.237
105
c HMN022 Human T-Cell Leukemia Virus Type 2 34 1.219
106
NSY001 N Syndrome 34 1.191
107
MYL055 Myeloid/lymphoid or Mixed Lineage Leukemia 24 1.189
108
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 6 1.186
109
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 6 1.175
110
c ACT195 Acute Myeloid Leukemia with T(9;11)(p22;q23) 18 1.172
111
ACT217 Acute Myeloid Leukemia with Recurrent Genetic Anomaly 4 1.168
112
THR106 Therapy Related Acute Myeloid Leukemia and Myelodysplastic Syndrome 7 1.166
113
ACT224 Acute Promyelocytic Leukemia Pml/rara Type 4 1.162
114
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 1.149
115
c HMN023 Human T-Cell Leukemia Virus Type 3 8 1.141
116
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 18 1.139
117
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 12 1.133
118
c ACT194 Acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation 26 1.131
119
ALK014 Aleukemic Mast Cell Leukemia 12 1.124
120
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 21 1.121
121
c ACT198 Acute Myeloid Leukemia with T(6;9)(p23;q34) 13 1.121
122
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 12 1.121
123
PRC009 Precursor T-Lymphoblastic Lymphoma/leukemia Refractory 5 1.118
124
DFN226 Deafness - Lymphedema - Leukemia 19 1.114
125
P ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 17 1.114
126
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 11 1.114
127
FML314 Familial Platelet Syndrome with Predisposition to Acute Myelogenous Leukemia 12 1.110
128
BLN016 Bilineal Acute Leukemia 9 1.110
129
c MYL018 Myelocytic Leukemia-Like Syndrome, Familial, Chronic 4 1.110
130
UNC013 Unclassified Acute Myeloid Leukemia 4 1.105
131
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 13 1.101
132
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 12 1.101
133
MGK005 Megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13) 9 1.101
134
CLS019 Classic Mast Cell Leukemia 6 1.101
135
ACT223 Acute Promyelocytic Leukemia Numa/rara Type 4 1.101
136
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 2 1.101
137
c ACT220 Acute Myeloid Leukemia, Kit-Related 8 1.095
138
c NPM001 Npm1-Related Acute Myeloid Leukemia 8 1.095
139
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 7 1.095
140
c ACT221 Acute Myeloid Leukemia, Somatic Dnmt3a-Related 7 1.095
141
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 7 1.095
142
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 7 1.095
143
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 5 1.095
144
WTL001 Wt Limb Blood Syndrome 19 1.080
145
MYL054 Myeloid and Lymphoid Neoplasm with Fgfr1 Abnormalities 10 1.080
146
LYM023 Lymphatic System Cancer 20 0.371
147
LYM036 Lymphatic Neoplasm 3 0.371
148
LYM024 Lymphatic System Disease 36 0.368
149
BNM001 Bone Marrow Cancer 47 0.366
150
P APL001 Aplastic Anemia 70 0.361
151
c HYP073 Hypersensitivity Reaction Type Iv Disease 28 0.320
152
BNC003 Bone Cancer 50 0.320
153
MYL009 Myelodysplastic Syndrome 69 0.317
154
BRK010 Burkitt Lymphoma 68 0.306
155
c ADL001 Adult Lymphoma 19 0.305
156
LYM019 Lymphosarcoma 47 0.304
157
c PRM046 Primary Malignant Lymphoma 30 0.265
158
c CHR092 Chronic Myeloproliferative Disease 39 0.257
159
HMT002 Hematologic Cancer 53 0.251
160
HMT018 Hematopoietic Stem Cell Transplantation 45 0.245
161
P BCL006 B-Cell Lymphomas 57 0.232
162
RFR004 Refractory Hematologic Cancer 22 0.217
163
c MCL062 Mucolipidosis Ii Alpha/beta 55 0.217
164
c PRM023 Pre-Malignant Neoplasm 29 0.209
165
BNL002 Bone Lymphoma 27 0.201
166
BNS002 Bone Structure Disease 24 0.197
167
ADL002 Adult Syndrome 43 0.187
168
GMM002 Gamma Chain Deficiency 44 0.178
169
LYM115 Lymphoma, Non-Hodgkin 62 0.177
170
MYL004 Myelodysplastic Myeloproliferative Cancer 35 0.177
171
c CNT033 Central Nervous System Cancer 45 0.172
172
PLV005 Pelviureteric Junction Obstruction 36 0.171
173
PRM151 Primary Bone Lymphoma 16 0.170
174
P NRV006 Nervous System Cancer 44 0.170
175
PRP021 Peripheral Nervous System Neoplasm 34 0.170
176
P MYL007 Myeloma 54 0.167
177
HPT023 Hepatocellular Carcinoma 90 0.160
178
CHR084 Chromosomal Disease 30 0.154
179
c MLT019 Multiple Myeloma 77 0.152
180
P ACT135 Acute Graft Versus Host Disease 44 0.149
181
SRC014 Sarcoma 57 0.144
182
DFC004 Deficiency Anemia 52 0.143
183
c SCN006 Secondary Syphilis 48 0.143
184
LKC003 Leukocyte Disease 28 0.141
185
RFR010 Refractory Anemia 38 0.141
186
GRF001 Graft-Versus-Host Disease, Protection Against 44 0.137
187
P NTR004 Neutropenia 50 0.135
188
BND014 Bone Development Disease 28 0.134
189
FRB001 Farber Lipogranulomatosis 53 0.132
190
P CNT005 Central Nervous System Lymphoma 44 0.131
191
c CHR417 Chronic Graft Versus Host Disease 41 0.131
192
PLS009 Plasma Cell Neoplasm 45 0.130
193
P MYL005 Myelofibrosis 64 0.130
194
CHL071 Child Syndrome 51 0.129
195
KDS001 Kid Syndrome 44 0.129
196
BLD053 Blood Platelet Disease 32 0.128
197
HDG012 Hodgkin Lymphoma 75 0.128
198
c CLL013 Cell Type Cancer 33 0.127
199
c LYM106 Lymphoproliferative Syndrome 1 23 0.126
200
c LYM107 Lymphoproliferative Syndrome 2 22 0.124
201
MNT001 Mantle Cell Lymphoma 60 0.122
202
PDT001 Pediatric Lymphoma 27 0.121
203
GDS001 Good Syndrome 37 0.121
204
WLL006 Wells Syndrome 48 0.120
205
END072 Endotheliitis 39 0.119
206
DWN001 Down Syndrome 62 0.118
207
CSY001 C Syndrome 44 0.118
208
NNS006 Non-Suppurative Otitis Media 36 0.117
209
BLD054 Blood Protein Disease 24 0.116
210
ATN003 Autonomic Nervous System Neoplasm 28 0.114
211
PRP036 Peripheral T-Cell Lymphoma 37 0.114
212
c CNT058 Central Nervous System Lymphoma, Primary 27 0.114
213
ORL011 Oral Cancer 43 0.113
214
CNT010 Central Nervous System Hematologic Cancer 9 0.113
215
HRT007 Heart Cancer 34 0.113
216
RPR002 Reproductive System Disease 26 0.113
217
P HRT017 Heart Tumor 21 0.113
218
P TRC086 Trichohepatoenteric Syndrome 1 42 0.111
219
P RFR008 Refractory Anemia with Excess Blasts 28 0.110
220
P ORL007 Oral Cavity Cancer 47 0.110
221
P ESN007 Eosinophilia 48 0.109
222
c ADL079 Adult Heart Tumor 7 0.108
223
P BRS047 Breast Cancer 100 0.108
224
RTC005 Reticulosarcoma 42 0.108
225
GRN017 Granulocytopenia 36 0.108
226
VND001 Vein Disease 34 0.107
227
P THR014 Thrombocytopenia 50 0.107
228
P KDN017 Kidney Cancer 60 0.105
229
SML025 Small Non-Cleaved Cell Lymphoma 17 0.105
230
HML018 Homologous Wasting Disease 9 0.105
231
DFF005 Diffuse Large B-Cell Lymphoma 48 0.103
232
P FLL037 Follicular Lymphoma 62 0.103
233
P HPT021 Hepatitis 58 0.102
234
ARG006 Aregenerative Anemia 17 0.101
235
P MST009 Mastocytosis 48 0.101
236
GST014 Gastrointestinal Lymphoma 23 0.101
237
THR013 Thoracic Outlet Syndrome 47 0.100
238
MCR004 Macroglobulinemia 43 0.099
239
THR004 Thrombocytosis 48 0.098
240
P ATX030 Ataxia-Telangiectasia 76 0.098
241
P INF038 Influenza 64 0.098
242
P ASP006 Aspergillosis 56 0.096
243
MYL003 Myeloid Sarcoma 41 0.095
244
RFR001 Refractory Plasma Cell Neoplasm 4 0.095
245
RFR007 Refractory Anemia with Excess Blasts in Transformation 17 0.094
246
P SPS003 Spastic Diplegia 37 0.094
247
MLN008 Melanoma 54 0.093
248
c RFR015 Refractory Anemia with Excess Blasts Type 1 9 0.093
249
P PNM007 Pneumonia 56 0.092
250
FCT013 Factor V Leiden Thrombophilia 43 0.092
251
c RFR014 Refractory Anemia with Excess Blasts Type 2 9 0.092
252
AND015 Androgen Insensitivity 65 0.091
253
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.091
254
P HML002 Hemolytic Anemia 52 0.091
255
ALR002 Al-Raqad Syndrome 23 0.091
256
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.090
257
c SPN225 Spondyloarthropathy 1 66 0.090
258
P ANG001 Angelman Syndrome 66 0.090
259
c ART101 Aortic Valve Disease 2 46 0.090
260
c BNG076 Benign Exophthalmos Syndrome 21 0.090
261
ANR002 Aniridia 72 0.089
262
P FML161 Familial Mediterranean Fever, Ar 67 0.089
263
PCK002 Pick Disease 61 0.089
264
ACN002 Acanthosis Nigricans 53 0.089
265
MRG003 Marginal Zone B-Cell Lymphoma 41 0.089
266
MXD023 Mixed Cell Type Cancer 33 0.089
267
RDT005 Radiation Induced Cancer 20 0.089
268
CYT008 Cytomegalovirus Infection 47 0.089
269
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.089
270
P ATX010 Ataxia Neuropathy Spectrum 31 0.089
271
PRS047 Prostatitis 50 0.088
272
ATN002 Autonomic Nervous System Disease 27 0.087
273
VSC006 Vascular Cancer 40 0.087
274
c ATM010 Autoimmune Hemolytic Anemia 56 0.086
275
TFT003 Tufting Enteropathy 27 0.086
276
P BRD002 Bardet-Biedl Syndrome 68 0.086
277
WLM007 Wilms Tumor Susceptibility-5 61 0.086
278
c BRD010 Bardet-Biedl Syndrome 1 59 0.086
279
P PLY018 Polycythemia 53 0.086
280
c CNT035 Central Nervous System Disease 52 0.086
281
P MNN013 Meningitis 51 0.086
282
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 39 0.085
283
P PNC044 Pancreatitis 51 0.084
284
HRT029 Heart Tumor of the Child 7 0.084
285
P ESS003 Essential Thrombocythemia 63 0.084
286
HRT003 Heart Lymphoma 17 0.084
287
ART001 Arterial Tortuosity Syndrome 59 0.083
288
P AND016 Andersen Syndrome 58 0.083
289
PRP019 Peripheral Nervous System Disease 31 0.083
290
P HYP004 Hypercalcemia 52 0.082
291
LYM012 Lymphoplasmacytic Lymphoma 40 0.082
292
RCH001 Richter's Syndrome 38 0.082
293
IRN002 Iron Metabolism Disease 36 0.082
294
c FLL041 Follicular Lymphoma 1 17 0.082
295
P LNG032 Lung Cancer 91 0.082
296
P WLD002 Waldenstrom Macroglobulinemia 57 0.081
297
SMT008 Smith-Magenis Syndrome 54 0.081
298
c PND001 Pain Disorder 43 0.081
299
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 29 0.081
300
GLC077 Glucocorticoid Therapy, Response to 6 0.081
301
VSC008 Vascular Hemostatic Disease 22 0.081
302
P PRS040 Prostate Cancer 90 0.080
303
P HST010 Histiocytosis 51 0.079
304
LPD004 Lipoid Nephrosis 38 0.079
305
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 33 0.079
306
P INF032 Infertility 52 0.078
307
VRL011 Viral Infectious Disease 50 0.078
308
P NRP001 Neuropathy 48 0.078
309
SCT005 Scott Syndrome 43 0.078
310
PLS025 Plasmablastic Lymphoma 38 0.078
311
ADS002 Adie Syndrome 34 0.078
312
HPT074 Hepatic Adenoma, Somatic 30 0.078
313
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 29 0.078
314
HNM002 Hinman Syndrome 27 0.078
315
P RHM011 Rheumatoid Arthritis 88 0.077
316
IMG001 Image Syndrome 56 0.077
317
MLL005 Miller-Dieker Syndrome 50 0.077
318
SPL004 Splenic Marginal Zone Lymphoma 38 0.077
319
P NRF002 Neurofibromatosis 66 0.077
320
P ART022 Arthritis 61 0.077
321
P THY032 Thyroiditis 48 0.077
322
GLC006 Galactosemia 76 0.076
323
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 33 0.076
324
P MTH007 Methemoglobinemia 44 0.075
325
P CRN214 Coronary Heart Disease 5 10 0.075
326
ABT001 Abetalipoproteinemia 57 0.074
327
MNT061 Mental Retardation-Hypotonic Facies Syndrome, X-Linked 41 0.074
328
P CHR345 Chronic Pain 39 0.074
329
P CMP010 Complex Regional Pain Syndrome 51 0.074
330
PRR002 Pure Red-Cell Aplasia 43 0.074
331
SPL012 Splenic Disease 37 0.074
332
MYL015 Myeloproliferative Disorder with Eosinophilia 29 0.074
333
TRP002 Tropical Spastic Paraparesis 51 0.073
334
EVN001 Evans' Syndrome 46 0.073
335
BNM005 Bone Marrow Necrosis 24 0.073
336
SPL011 Spleen Cancer 23 0.073
337
c CRN178 Coronary Heart Disease 6 10 0.073
338
SPS057 Spasticity 30 0.072
339
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 30 0.072
340
SPS019 Spastic Paraparesis 27 0.072
341
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.072
342
LRN003 Learning Disability 47 0.071
343
HYP266 Hypoxia 42 0.071
344
EMN001 Emanuel Syndrome 38 0.071
345
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.071
346
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 18 0.071
347
c FNC027 Fanconi Anemia, Complementation Group a 71 0.070
348
SVR004 Severe Combined Immunodeficiency 65 0.070
349
P CTN015 Cutaneous T Cell Lymphoma 45 0.069
350
NNH003 Non-Hodgkin Lymphoma, Childhood 4 0.069
351
GLC037 Glucocorticoid Resistance 51 0.069
352
VHW001 Vohwinkel Syndrome 50 0.069
353
IPX001 Ipex Syndrome 43 0.069
354
NDL020 Nodal Marginal Zone B-Cell Lymphoma 26 0.069
355
PLL005 Pallister-Killian Mosaic Syndrome 18 0.069
356
LYM048 Lymphoma, Large-Cell, Immunoblastic 14 0.069
357
PLY125 Polycythemia Vera, Somatic 62 0.068
358
P RCK004 Rickets 55 0.068
359
DSS009 Disseminated Intravascular Coagulation 48 0.068
360
MTH009 Mouth Disease 44 0.068
361
NTR005 Nutritional Deficiency Disease 41 0.068
362
SPN035 Spindle Cell Sarcoma 41 0.068
363
LKS001 Leukostasis 35 0.068
364
MYC002 Mycobacterium Avium Complex Disease 46 0.067
365
BRD005 Borderline Leprosy 40 0.067
366
c MCR161 Macroglobulinemia, Waldenstrom 1 20 0.067
367
c MCR162 Macroglobulinemia, Waldenstrom 2 11 0.067
368
LYM050 Lymphoma, Small Cleaved-Cell, Follicular 5 0.067
369
P HNT016 Huntington Disease 78 0.066
370
P CNG401 Congenital Heart Disease 68 0.066
371
P PRM002 Primary Hyperoxaluria 64 0.066
372
P ADN016 Adenocarcinoma 56 0.066
373
WST001 West Syndrome 54 0.066
374
P ACR001 Aicardi-Goutieres Syndrome 53 0.066
375
c MTB001 Metabolic Syndrome X 52 0.066
376
SML033 Small Cell Cancer of the Lung, Somatic 43 0.066
377
c CMP058 Complex Regional Pain Syndrome Type 1 40 0.066
378
c THR090 Thrombocythemia 1 30 0.066
379
WTH001 Withdrawal Disorder 27 0.066
380
PLL001 Pallister-Hall Syndrome 60 0.065
381
P PTT014 Pitt-Hopkins Syndrome 55 0.065
382
P KBK002 Kabuki Syndrome 1 47 0.065
383
UTR033 Uterine Corpus Cancer 38 0.065
384
HDG004 Hodgkin's Granuloma 27 0.065
385
c CRN173 Coronary Heart Disease 8 9 0.065
386
ALC007 Alcohol Dependence 59 0.065
387
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 48 0.065
388
c INF069 Infantile Neuroaxonal Dystrophy 1 46 0.065
389
VSC011 Vasculitis 50 0.064
390
P CYS036 Cystinosis, Nephropathic 48 0.064
391
P ATX004 Ataxia 43 0.064
392
BCT015 Bacteremia 40 0.064
393
c HRD009 Hereditary Wilms' Tumor 29 0.064
394
DSS003 Disseminated Eosinophilic Collagen Disease 9 0.064
395
P CNT061 Conotruncal Heart Malformations 59 0.063
396
HNT002 Hantavirus Pulmonary Syndrome 52 0.063
397
P ANP001 Anaplastic Large Cell Lymphoma 47 0.063
398
PST046 Post-Transplant Lymphoproliferative Disease 44 0.063
399
SPN060 Spondylocarpotarsal Synostosis Syndrome 41 0.063
400
TRN060 Truncus Arteriosus 40 0.063
401
CRB009 Cerebritis 37 0.063
402
MCR039 Macrophagic Myofasciitis 28 0.063
403
MGK002 Megakaryocytic Tumor 20 0.063
404
HDG006 Hodgkin's Paragranuloma 15 0.063
405
P RNL014 Renal Cell Carcinoma 81 0.062
406
c PRK057 Parkinson Disease, Late-Onset 73 0.062
407
P PND002 Pendred Syndrome 63 0.062
408
MYC006 Mycosis Fungoides 60 0.062
409
P AST007 Astrocytoma 55 0.062
410
THR100 Thrombocytopenic Purpura, Autoimmune 47 0.062
411
PLS011 Plasmacytoma 46 0.062
412
RTN023 Retinitis 43 0.062
413
c PRM149 Primary Hypereosinophilic Syndrome 29 0.062
414
c THR037 Thrombocytopenia 2 28 0.062
415
P CLR023 Colorectal Cancer 95 0.061
416
BRN028 Brain Cancer 59 0.061
417
PRL019 Prolidase Deficiency 44 0.061
418
P EHL015 Ehlers-Danlos Syndrome Progeroid Type 39 0.061
419
BNM011 Bone Marrow Failure Syndrome 2 20 0.061
420
P ALZ034 Alzheimer Disease 98 0.061
421
c NRF018 Neurofibromatosis, Type 1 63 0.061
422
P GLB002 Glioblastoma 53 0.061
423
CHN055 Chanarin-Dorfman Syndrome 51 0.061
424
c SVR003 Severe Congenital Neutropenia 49 0.061
425
ACT049 Acute Disseminated Encephalomyelitis 49 0.061
426
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 48 0.061
427
SFT003 Soft Tissue Sarcoma 48 0.061
428
P PNC001 Pancytopenia 41 0.061
429
P NRB001 Neuroblastoma 73 0.060
430
OST003 Osteonecrosis 50 0.060
431
KRT002 Keratomalacia 49 0.060
432
c CNG124 Congenital Rubella 47 0.060
433
DPH001 Diphtheria 47 0.060
434
SPN012 Spindle Cell Hemangioma 33 0.060
435
c CRN159 Craniosynostosis, Type 1 32 0.060
436
RMR001 Ramer Ladda Syndrome 23 0.060
437
IND005 Indolent B Cell Lymphoma 18 0.060
438
RNL005 Renal Wilms' Tumor 17 0.060
439
c CRN177 Coronary Heart Disease 7 10 0.060
440
P CWD001 Cowden Disease 64 0.059
441
MSM014 Mismatch Repair Cancer Syndrome 58 0.059
442
RBR001 Roberts Syndrome 54 0.059
443
CLT003 Colitis 47 0.059
444
RCT018 Rectal Neoplasm 43 0.059
445
HMG002 Hemoglobinuria 39 0.059
446
c CWD006 Cowden Syndrome 1 39 0.059
447
PRL032 Perlman Syndrome 38 0.059
448
ADJ001 Adjustment Disorder 30 0.059
449
c CHR096 Chronic Pulmonary Heart Disease 30 0.059
450
c TRC078 Trichohepatoenteric Syndrome 2 20 0.059
451
P RTN024 Retinoblastoma 74 0.058
452
THY028 Thyroid Cancer 60 0.058
453
CHR066 Chronic Fatigue Syndrome 55 0.058
454
c MLG054 Malignant Histiocytosis 44 0.058
455
c RTN162 Retinitis Pigmentosa 2 43 0.058
456
MPH001 Mephenytoin Poor Metabolizer 25 0.058
457
c SLC031 Slco1b1-Related Altered Drug Metabolism 13 0.058
458
WSC001 Wisconsin Syndrome 4 0.058
459
HV1006 Hiv-1 77 0.057
460
P KDN018 Kidney Disease 57 0.057
461
MVL001 Mevalonic Aciduria 54 0.057
462
RHB003 Rhabdomyosarcoma 51 0.057
463
WHM001 Whim Syndrome 47 0.057
464
GRD007 Grade Iii Astrocytoma 44 0.057
465
SPL018 Splenomegaly 34 0.057
466
CHR178 Chromosomal Triplication 23 0.057
467
BNM010 Bone Marrow Failure Syndrome 1 20 0.057
468
PRP030 Purpura 47 0.056
469
TTR011 Tetraploidy 37 0.056
470
MDS022 Mediastinitis 33 0.056
471
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 21 0.056
472
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.055
473
PRP027 Peripheral Vascular Disease 62 0.055
474
MSM001 Meesmann Corneal Dystrophy 42 0.055
475
P CRV039 Cervicitis 42 0.055
476
P PRP023 Peripheral Neuropathy 40 0.055
477
LKM001 Leukemoid Reaction 35 0.055
478
SKN023 Skin Tag 33 0.055
479
DND018 Dendritic Cell Tumor 32 0.055
480
LNG013 Lung Lymphoma 28 0.055
481
c CRN176 Coronary Heart Disease 9 9 0.055
482
WHT007 White Platelet Syndrome 8 0.055
483
c SML023 Small Cell Lung Cancer, Adult 5 0.055
484
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 75 0.054
485
P STH001 Saethre-Chotzen Syndrome 65 0.054
486
c CHR089 Chronic Kidney Failure 61 0.054
487
c MNN043 Meningioma, Familial 55 0.054
488
P SHR029 Short Syndrome 49 0.054
489
P ACT105 Acute Mountain Sickness 46 0.054
490
P GLM040 Glioma Susceptibility 1 43 0.054
491
c CHL119 Cholangitis, Primary Sclerosing 30 0.054
492
ENG004 Engraftment Syndrome 22 0.054
493
CRH001 Crohn's Disease 80 0.053
494
GST019 Gastrointestinal Stromal Tumor 68 0.053
495
DRM006 Dermatitis 54 0.053
496
NWC001 Newcastle Disease 45 0.053
497
LYM051 Lymphomatoid Granulomatosis 39 0.053
498
LYM020 Lymph Node Cancer 31 0.053
499
P HYP253 Hypohidrotic Ectodermal Dysplasia, Autosomal 27 0.053
500
P ACT080 Acute Pulmonary Heart Disease 20 0.053
501
c HPT001 Hepatitis C 64 0.052
502
SKN016 Skin Disease 61 0.052
503
HRP004 Herpes Zoster 54 0.052
504
GNG013 Gingivitis 47 0.052
505
P HML001 Hemolytic-Uremic Syndrome 44 0.052
506
c INV001 Invasive Aspergillosis 40 0.052
507
TST015 Testicular Disease 37 0.052
508
LYM116 Lymph Node Disease 31 0.052
509
P OVR042 Ovarian Cancer 69 0.051
510
LNG024 Langerhans-Cell Histiocytosis 63 0.051
511
P AMY004 Amyloidosis 60 0.051
512
c HPT016 Hepatitis B 59 0.051
513
HYP066 Hyperglycemia 50 0.051
514
ATX019 Ataxia with Vitamin E Deficiency 49 0.051
515
P GLM007 Glomerulonephritis 49 0.051
516
P DBT005 Diabetes Insipidus 46 0.051
517
MST017 Mast Cell Disease 43 0.051
518
GNT002 Giant Cell Glioblastoma 43 0.051
519
c EYC002 Eye Carcinoma 38 0.051
520
GMS001 Gemistocytic Astrocytoma 37 0.051
521
MNC006 Monoclonal Gammopathy of Uncertain Significance 37 0.051
522
FXF001 Fox Fordyce Disease 28 0.051
523
ACQ031 Acquired Idiopathic Sideroblastic Anemia 20 0.051
524
c THR048 Thrombocytopenia 4 20 0.051
525
YNG002 Young Syndrome 16 0.051
526
c WLM005 Wilms Tumor 2 15 0.051
527
c ANP011 Anaplastic Small Cell Lymphoma 6 0.051
528
P OBS005 Obesity 89 0.050
529
WLL001 Williams-Beuren Syndrome 59 0.050
530
BRC012 Brucellosis 55 0.050
531
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.050
532
GRN039 Greenberg Skeletal Dysplasia 43 0.050
533
MTT002 Metatropic Dysplasia 40 0.050
534
NRN002 Neuronitis 40 0.050
535
P HYP071 Hypersensitivity Reaction Type Ii Disease 38 0.050
536
P GRN010 Granular Cell Tumor 38 0.050
537
PLY031 Polydactyly Myopia Syndrome 29 0.050
538
c THR087 Thrombocythemia 2 24 0.050
539
AND005 Androgen Insensitivity Syndrome, Mild 19 0.050
540
VSC001 Vascular Myelopathy 13 0.050
541
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 5 0.050
542
KWS002 Kawasaki Disease 62 0.049
543
CNN005 Connective Tissue Disease 49 0.049
544
SZR001 Sezary's Disease 48 0.049
545
PRG009 Progressive Multifocal Leukoencephalopathy 45 0.049
546
P THR012 Thoracic Cancer 44 0.049
547
MRC001 Marchiafava Bignami Disease 42 0.049
548
MN1001 Mn1 25 0.049
549
SPC003 Specific Developmental Disorder 25 0.049
550
CNG034 Congestive Heart Failure 65 0.048
551
P HRM001 Hermansky-Pudlak Syndrome 62 0.048
552
c HPT073 Hepatitis C Virus 60 0.048
553
TYP007 Typhoid Fever 59 0.048
554
EWN003 Ewing Sarcoma 55 0.048
555
P CND004 Candidiasis 50 0.048
556
P NRV007 Nervous System Disease 49 0.048
557
c PRM012 Primary Polycythemia 48 0.048
558
GLS001 Gliosarcoma 45 0.048
559
PRC012 Pericardial Effusion 41 0.048
560
BWN003 Bowenoid Papulosis 34 0.048
561
FML039 Female Reproductive System Disease 28 0.048
562
SML011 Smoldering Myeloma 26 0.048
563
MNG003 Mungan Syndrome 24 0.048
564
ANP010 Anaplastic Plasmacytoma 17 0.048
565
TBR010 Tuberculosis 64 0.047
566
P HRP006 Herpes Simplex 60 0.047
567
TST014 Testicular Cancer 51 0.047
568
ICH002 Ichthyosis Bullosa of Siemens 51 0.047
569
P CNJ013 Conjunctivitis 50 0.047
570
ZYG002 Zygomycosis 35 0.047
571
P CNN004 Connective Tissue Cancer 31 0.047
572
CHL060 Childhood Kidney Neoplasm 28 0.047
573
CHP002 Chops Syndrome 27 0.047
574
MND006 Mondor Disease 21 0.047
575
ACT162 Acute Sensory Ataxic Neuropathy 17 0.047
576
CHR208 Chromosome 17p Deletion 16 0.047
577
MYL052 Myeloproliferative Neoplasms, Familial 8 0.047
578
c SCN042 Secondary Hypereosinophilic Syndrome 8 0.047
579
LYM041 Lymphocytes Absent 5 0.047
580
P MYC007 Myocardial Infarction 76 0.046
581
P OST002 Osteoporosis 75 0.046
582
P MDL022 Medullary Thyroid Carcinoma, Familial 56 0.046
583
HMR001 Hemorrhagic Thrombocythemia 48 0.046
584
P PLY019 Polyneuropathy 46 0.046
585
SPN020 Spondylosis 46 0.046
586
P MST018 Mesothelioma 45 0.046
587
NRF007 Neurofibroma 45 0.046
588
P HYP014 Hyperuricemia 45 0.046
589
NRC020 Neuroectodermal Tumor 43 0.046
590
PNC033 Pancreas Adenocarcinoma 36 0.046
591
PLX002 Plexiform Neurofibroma 36 0.046
592
HST016 Histiocytic Sarcoma 35 0.046
593
FSR001 Fusariosis 33 0.046
594
ANG046 Angioimmunoblastic T-Cell Lymphoma 33 0.046
595
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.046
596
CRB001 Cerebral Lymphoma 29 0.046
597
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 28 0.046
598
c CNN010 Connective Tissue Benign Neoplasm 28 0.046
599
HYP084 Hypopyon 26 0.046
600
GRN008 Granular Cell Carcinoma 23 0.046
601
PRM133 Primary Pulmonary Lymphoma 17 0.046
602
c CRN175 Coronary Heart Disease 4 9 0.046
603
STT009 Sutton Disease 2 7 0.046
604
DWS002 Dawson Disease 3 0.046
605
P NJM001 Nijmegen Breakage Syndrome 62 0.045
606
OST085 Osteosarcoma, Somatic 56 0.045
607
CMP002 Campylobacteriosis 49 0.045
608
TXC002 Toxic Encephalopathy 43 0.045
609
PKL001 Poikiloderma with Neutropenia 43 0.045
610
GRM005 Germ Cell Cancer 43 0.045
611
TLN003 Telangiectasis 41 0.045
612
CNV002 Conversion Disorder 37 0.045
613
HPT070 Hepatosplenic T-Cell Lymphoma 37 0.045
614
PRM025 Primary Bacterial Infectious Disease 27 0.045
615
PRM087 Premature Chromatid Separation Trait 24 0.045
616
NVD002 Nevada Syndrome 7 0.045
617
HDG009 Hodgkin Lymphoma, Childhood 5 0.045
618
c SYS001 Systemic Lupus Erythematosus 90 0.043
619
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.043
620
P PLM037 Pulmonary Hypertension 78 0.043
621
c SYS005 Systemic Scleroderma 62 0.043
622
c PNC108 Pancreatitis, Hereditary 59 0.043
623
P RSP003 Respiratory Failure 58 0.043
624
PRP032 Porphyria Variegata 54 0.043
625
c ALM001 Al Amyloidosis 45 0.043
626
P MYS033 Miyoshi Muscular Dystrophy 1 44 0.043
627
P SKN013 Skin Benign Neoplasm 39 0.043
628
FLL019 Follicular Mucinosis 35 0.043
629
OVR094 Ovarian Epithelial Cancer 33 0.043
630
BCK006 Back Pain 32 0.043
631
CMP001 Composite Lymphoma 30 0.043
632
WRT001 Worth's Syndrome 25 0.043
633
P VLC001 Velocardiofacial Syndrome 61 0.042
634
CRV047 Cervical Cancer, Somatic 61 0.042
635
P LPS004 Lupus Erythematosus 61 0.042
636
P PRP029 Porphyria 54 0.042
637
P CRD011 Cardiomyopathy 53 0.042
638
CHR020 Chronic Interstitial Cystitis 53 0.042
639
PRT011 Protein C Deficiency 46 0.042
640
MLL012 Miller Syndrome 41 0.042
641
P PLM006 Pulmonary Alveolar Proteinosis 41 0.042
642
OBS001 Obstructive Jaundice 40 0.042
643
MNT002 Mental Depression 39 0.042
644
MTR008 Mature B-Cell Neoplasm 31 0.042
645
BTH002 Bothnia Retinal Dystrophy 27 0.042
646
MNN041 Mannose-Binding Lectin Protein Deficiency 18 0.042
647
CHR062 Chronic Erythremia 5 0.042
648
WLS001 Wilson Disease 74 0.041
649
P MDL005 Medulloblastoma 69 0.041
650
c HYP595 Hypertension, Essential 68 0.041
651
MLG068 Malignant Glioma 57 0.041
652
ACQ007 Acquired Immunodeficiency Syndrome 55 0.041
653
P MYS005 Myositis 54 0.041
654
APP008 Appendicitis 52 0.041
655
SCR002 Scurvy 51 0.041
656
PPL022 Papilloma 49 0.041
657
c THR092 Thrombophilia Due to Thrombin Defect 49 0.041
658
P UVT001 Uveitis 49 0.041
659
MGL001 Megaloblastic Anemia 47 0.041
660
PMP001 Pemphigus 45 0.041
661
c JVN003 Juvenile Xanthogranuloma 40 0.041
662
AGG002 Aggressive Systemic Mastocytosis 39 0.041
663
CRP017 Carpal Tunnel Syndrome, Familial 39 0.041
664
P SDR003 Sideroblastic Anemia 38 0.041
665
HYP025 Hyperphosphatemia 36 0.041
666
TMP012 Temple Syndrome 32 0.041
667
GLB003 Globe Disease 22 0.041
668
P EYL003 Eye Lymphoma 20 0.041
669
c THR086 Thrombocythemia 3 19 0.041
670
c DLT001 Delta Chain Disease 5 0.041
671
PRP003 Porphyria Cutanea Tarda 69 0.040
672
P DMN001 Diamond-Blackfan Anemia 66 0.040
673
GLN010 Glanzmann Thrombasthenia 65 0.040
674
PTR006 Peters Anomaly 63 0.040
675
P ALX003 Alexander Disease 61 0.040
676
VSC007 Vascular Disease 55 0.040
677
END030 End Stage Renal Failure 51 0.040
678
P THY023 Thymoma 50 0.040
679
LYM021 Lymphadenitis 48 0.040
680
c ACT027 Acute Pancreatitis 47 0.040
681
TTH006 Tooth Disease 47 0.040
682
PRD019 Periodic Fever, Familial 46 0.040
683
CTN014 Cutaneous Mastocytosis 45 0.040
684
P END033 Endocarditis 43 0.040
685
P BRN009 Burning Mouth Syndrome 42 0.040
686
PYM001 Pyomyositis 41 0.040
687
GST053 Gastric Cancer 41 0.040
688
SPN021 Spinal Meningioma 39 0.040
689
SPN040 Spinal Cancer 37 0.040
690
CMB003 Combined T Cell and B Cell Immunodeficiency 35 0.040
691
MLN012 Melanoma and Neural System Tumor Syndrome 33 0.040
692
CYC007 Cyclic Thrombocytopenia 29 0.040
693
MLG097 Malignant Mesenchymal Tumor 28 0.040
694
c THR102 Thrombocytopenia 5 19 0.040
695
BRN049 Brain Tumor, Childhood 14 0.040
696
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 13 0.040
697
CNT098 Central Core Disease 60 0.038
698
KLN001 Klinefelter's Syndrome 57 0.038
699
P MCP010 Mucopolysaccharidosis 53 0.038
700
PRP025 Peripheral Primitive Neuroectodermal Tumor 52 0.038
701
c ACT075 Acute Myocardial Infarction 50 0.038
702
BRN012 Bronchiolitis Obliterans 49 0.038
703
NTR040 Neutropenia, Cyclic 49 0.038
704
BRN002 Bronchiolitis 48 0.038
705
P GST049 Gastrointestinal System Cancer 43 0.038
706
PRP007 Priapism 41 0.038
707
CLN015 Colon Adenocarcinoma 40 0.038
708
P LCT001 Lactic Acidosis 40 0.038
709
HMM002 Haim-Munk Syndrome 40 0.038
710
SQM002 Squamous Cell Papilloma 37 0.038
711
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 37 0.038
712
MHC001 Mhc Class Ii Deficiency 35 0.038
713
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 34 0.038
714
PHY002 Physical Disorder 33 0.038
715
CLV009 Clove Syndrome, Somatic 28 0.038
716
TTR021 Tetrasomy 21 20 0.038
717
ULC004 Ulcerative Colitis 75 0.037
718
GLL008 Gilles De La Tourette Syndrome 67 0.037
719
P RBN001 Rubinstein-Taybi Syndrome 66 0.037
720
TNG009 Tongue Squamous Cell Carcinoma 60 0.037
721
TST021 Testicular Germ Cell Tumor 60 0.037
722
P CHR071 Charcot-Marie-Tooth Disease 59 0.037
723
P ANT006 Antiphospholipid Syndrome 55 0.037
724
MLK003 Melkersson-Rosenthal Syndrome 53 0.037
725
MSL001 Measles 52 0.037
726
P ALP009 Alopecia Areata 52 0.037
727
SCB001 Scabies 46 0.037
728
CRY004 Cryoglobulinemia 45 0.037
729
CRS005 Crest Syndrome 45 0.037
730
RTN017 Retinal Detachment 44 0.037
731
MCP006 Mucoepidermoid Carcinoma 43 0.037
732
PSD002 Pseudotumor Cerebri 42 0.037
733
P ENC018 Encephalopathy 42 0.037
734
P EXN002 Exanthem 41 0.037
735
HYP063 Hypersplenism 40 0.037
736
DRR008 Diarrhea 1, Secretory Chloride, Congenital 40 0.037
737
P CNG003 Congenital Dyserythropoietic Anemia 37 0.037
738
CNG064 Congenital Chloride Diarrhea 36 0.037
739
CHR276 Chronic Active Epstein-Barr Virus Infection 35 0.037
740
P HVY001 Heavy Chain Disease 34 0.037
741
MST004 Mast Cell Neoplasm 33 0.037
742
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 32 0.037
743
c MLG049 Malignant Syringoma 31 0.037
744
P BLD051 Blood Coagulation Disease 30 0.037
745
HTL002 Htlv-1 Associated Myelopathy 29 0.037
746
TST004 Testicular Lymphoma 28 0.037
747
NSD001 Nose Disease 28 0.037
748
c PSR017 Psoriasis 2 28 0.037
749
P PSR004 Psoriasis Susceptibility 1 28 0.037
750
LPS020 Lipase Deficiency, Combined 28 0.037
751
c PSR019 Psoriasis Susceptibility 13 23 0.037
752
PSR005 Psoriasis, Protection Against 21 0.037
753
CYT018 Cytochrome P450 2d6 Variant 15 0.037
754
INS024 Insulin-Like Growth Factor I 64 0.035
755
P FRD001 Friedreich Ataxia 61 0.035
756
THR006 Thromboangiitis Obliterans 60 0.035
757
P LVR013 Liver Disease 59 0.035
758
P AGM001 Agammaglobulinemia 59 0.035
759
P FND001 Fundus Albipunctatus 54 0.035
760
P FTL001 Fetal Alcohol Syndrome 50 0.035
761
P MYP004 Myopathy 50 0.035
762
URT039 Urticaria 50 0.035
763
P SNS014 Sinusitis 49 0.035
764
P ENC004 Encephalitis 48 0.035
765
OST017 Osteomyelitis 48 0.035
766
P OLG002 Oligodendroglioma 48 0.035
767
TNS005 Tonsillitis 47 0.035
768
PYD001 Pyoderma Gangrenosum 46 0.035
769
MRK001 Merkel Cell Carcinoma 44 0.035
770
PRN011 Pernicious Anemia 44 0.035
771
c ACT134 Acute Liver Failure 44 0.035
772
ADR016 Adrenal Cortical Carcinoma 43 0.035
773
PPL002 Papillary Carcinoma 43 0.035
774
EWN002 Ewing's Family of Tumors 41 0.035
775
P TRT010 Teratoma 40 0.035
776
GRW007 Growth Hormone Deficiency 38 0.035
777
P HYP599 Hypoparathyroidism, Familial Isolated 38 0.035
778
PRN049 Paraneoplastic Pemphigus 38 0.035
779
INT054 Intraocular Lymphoma 37 0.035
780
GRN007 Granuloma Annulare 35 0.035
781
ECT004 Ecthyma 33 0.035
782
c BNG032 Benign Mesothelioma 32 0.035
783
CRN237 Corneal Dystrophy, Avellino Type 31 0.035
784
FTD001 Foot Drop 25 0.035
785
GRN016 Grant Syndrome 21 0.035
786
PRM128 Primary Cutaneous Follicle Center Lymphoma 19 0.035
787
CNT067 Central Cord Syndrome 16 0.035
788
ALD004 Ala Dehydratase Deficiency 12 0.035
789
NVS004 Nova Syndrome 11 0.035
790
c ALX007 Alexander Disease Type I 8 0.035
791
c FML303 Familial/multiple Cancer 6 0.035
792
INC002 Inclusion Body Myositis 67 0.034
793
c JVN010 Juvenile Rheumatoid Arthritis 64 0.034
794
P STM004 Stomach Cancer 63 0.034
795
P NNN008 Noonan Syndrome 1 62 0.034
796
P HYP117 Hypertriglyceridemia 56 0.034
797
P NPH012 Nephrotic Syndrome 52 0.034
798
CHL067 Cholecystitis 51 0.034
799
LST001 Listeriosis 51 0.034
800
P SML001 Small Cell Carcinoma 49 0.034
801
P FML035 Familial Hyperlipidemia 46 0.034
802
c LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 46 0.034
803
END021 Endomyocardial Fibrosis 44 0.034
804
PYD002 Pyoderma 41 0.034
805
CYT005 Cytomegalovirus Retinitis 40 0.034
806
CHL018 Childhood Medulloblastoma 40 0.034
807
ANP009 Anaplastic Oligodendroglioma 39 0.034
808
HYP017 Hypophosphatemia 39 0.034
809
P IDP064 Idiopathic Neutropenia 38 0.034
810
P LRG017 Large Intestine Cancer 37 0.034
811
RGH009 Right Atrial Isomerism 36 0.034
812
THY009 Thyroid Lymphoma 35 0.034
813
TCL003 T Cell Deficiency 35 0.034
814
SPN041 Spinal Cord Disease 33 0.034
815
INT253 Intestinal Benign Neoplasm 33 0.034
816
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 30 0.034
817
CYT004 Cytomegalic Inclusion Disease 27 0.034
818
CRB040 Cerebrum Cancer 27 0.034
819
BRS001 Breast Lymphoma 26 0.034
820
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 26 0.034
821
TRS012 Trisomy 22 24 0.034
822
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.034
823
ICH056 Ichthyosis-Hypotrichosis Syndrome 18 0.034
824
c ABC018 Abcb1-Related Altered Drug Metabolism 14 0.034
825
c ALX006 Alexander Disease Type Ii 9 0.034
826
MNT045 Montefiore Syndrome 1 0.034
827
P MYS003 Myasthenia Gravis 59 0.032
828
ADN018 Adenoma 54 0.032
829
EYD002 Eye Disease 54 0.032
830
RSC001 Rosacea 50 0.032
831
P ART023 Arthropathy 50 0.032
832
P LPS002 Liposarcoma 49 0.032
833
THY022 Thymic Carcinoma 48 0.032
834
PRN038 Prune Belly Syndrome 47 0.032
835
SLP005 Sleep Disorder 47 0.032
836
P LRY019 Laryngitis 46 0.032
837
P WLL002 Weill-Marchesani Syndrome 46 0.032
838
P PLY041 Polymyositis 45 0.032
839
INT007 Intermediate Coronary Syndrome 45 0.032
840
MMB001 Membranoproliferative Glomerulonephritis 44 0.032
841
GST027 Gastric Lymphoma 43 0.032
842
LYM027 Lymphopenia 43 0.032
843
CLL003 Cellulitis 41 0.032
844
EXT010 Extramedullary Plasmacytoma 40 0.032
845
STM007 Stomatitis 40 0.032
846
ATR013 Atrichia with Papular Lesions 39 0.032
847
HYP005 Hypokalemia 39 0.032
848
NRR001 Neuroretinitis 38 0.032
849
GLM011 Glomerulosclerosis 38 0.032
850
EMB003 Embryonal Cancer 38 0.032
851
PNN001 Panniculitis 37 0.032
852
MDL002 Medulloepithelioma 36 0.032
853
FML089 Familial Thoracic Aortic Aneurysm and Dissection 36 0.032
854
SPL006 Splenic Infarction 35 0.032
855
c LPD019 Lipodystrophy, Partial, Acquired 34 0.032
856
MCR095 Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 33 0.032
857
GLC086 Glucocorticoid-Induced Osteoporosis 33 0.032
858
CLB026 Colobomatous Microphthalmia 33 0.032
859
DYN001 Doyne Honeycomb Degeneration of Retina 31 0.032
860
ANG037 Angiomatosis 30 0.032
861
MCL014 Mcleod Neuroacanthocytosis Syndrome 28 0.032
862
CLD014 Cole Disease 28 0.032
863
VRS001 Virus Associated Hemophagocytic Syndrome 27 0.032
864
MCL055 Mcleod Syndrome with or Without Chronic Granulomatous Disease 26 0.032
865
MYC066 Myoclonus, Familial Cortical 26 0.032
866
RDN001 Reading Disorder 25 0.032
867
MDS018 Mediastinal Cancer 24 0.032
868
HYP591 Hypoplastic or Aplastic Tibia with Polydactyly 24 0.032
869
c RNG017 Ring Chromosome 21 24 0.032
870
MSC004 Muscle Tissue Disease 23 0.032
871
DSS022 Disseminated Peritoneal Leiomyomatosis 20 0.032
872
PHY001 Physiological Polycythemia 17 0.032
873
CRC034 Carcinoma Showing Thymus-Like Differentiation 17 0.032
874
TST022 Testicular Cancer, Childhood 4 0.032
875
P RTT002 Rett Syndrome 79 0.031
876
BLM001 Bloom Syndrome 63 0.031
877
P ADD001 Addison's Disease 60 0.031
878
SHW002 Shwachman-Diamond Syndrome 58 0.031
879
LBR002 Leber Hereditary Optic Neuropathy 58 0.031
880
BLD087 Bladder Cancer, Somatic 58 0.031
881
ANX002 Anxiety Disorder 57 0.031
882
P HYD011 Hydrolethalus Syndrome 57 0.031
883
DNG002 Dengue Hemorrhagic Fever 55 0.031
884
MXD005 Mixed Connective Tissue Disease 53 0.031
885
P TMP003 Temporal Arteritis 53 0.031
886
P HYP086 Hypothyroidism 52 0.031
887
ETN001 Eating Disorder 52 0.031
888
ACR003 Acrodermatitis Enteropathica 51 0.031
889
P HMP007 Hemophilia 51 0.031
890
STR008 Strongyloidiasis 50 0.031
891
P AVS004 Avascular Necrosis of the Femoral Head 49 0.031
892
P MMP001 Mumps 49 0.031
893
c INF071 Inflammatory Bowel Disease 1 48 0.031
894
NRT001 Neurotic Disorder 48 0.031
895
SPT004 Septic Arthritis 47 0.031
896
FLT001 Felty's Syndrome 47 0.031
897
P SCL015 Scleritis 45 0.031
898
HPT025 Hepatic Lipase Deficiency 45 0.031
899
PLM010 Pulmonary Edema 45 0.031
900
P FNC044 Fanconi Anemia, Complementation Group C 44 0.031
901
CRN036 Craniopharyngioma 44 0.031
902
PRC013 Pericarditis 44 0.031
903
CLD007 Cold Agglutinin Disease 43 0.031
904
c MLG081 Malignant Teratoma 41 0.031
905
PLR008 Pleurisy 41 0.031
906
c SPN317 Spinal Muscular Atrophy-3 39 0.031
907
GYN001 Gynecomastia 39 0.031
908
CRD001 Cardiac Tamponade 39 0.031
909
MNN014 Mononeuritis 39 0.031
910
CNG028 Congenital Hypoplastic Anemia 39 0.031
911
ACT100 Acute Febrile Neutrophilic Dermatosis 38 0.031
912
P CHR019 Choroid Plexus Carcinoma 38 0.031
913
NRW001 Norwegian Scabies 38 0.031
914
c SML034 Small Cell Neuroendocrine Carcinoma 38 0.031
915
DND002 Dendritic Cell Sarcoma 38 0.031
916
IDP021 Idiopathic Myopathy 38 0.031
917
CHR008 Choroiditis 37 0.031
918
HMC006 Homocystinuria Due to Mthfr Deficiency 36 0.031
919
P INT063 Intellectual Disability 36 0.031
920
P NRL007 Neurologic Diseases 35 0.031
921
P FRN036 Frontonasal Dysplasia 1 34 0.031
922
SPL007 Splenic Abscess 34 0.031
923
HMP001 Hemopericardium 33 0.031
924
c FML008 Familial Retinoblastoma 32 0.031
925
CRT009 Critical Illness Polyneuropathy 32 0.031
926
URT008 Urticaria Pigmentosa 32 0.031
927
c HYP602 Hyperoxaluria, Primary, Type Ii 32 0.031
928
c JVN006 Juvenile Spinal Muscular Atrophy 32 0.031
929
SXL003 Sexual Disorder 30 0.031
930
PRN039 Paraneoplastic Syndromes 27 0.031
931
MNC004 Monoclonal Paraproteinemia 24 0.031
932
P SML002 Small Cell Sarcoma 23 0.031
933
GRM001 Germ Cell and Embryonal Cancer 22 0.031
934
MTH027 Mthfr Deficiency 21 0.031
935
GNR023 Generalized Eruptive Histiocytosis 20 0.031
936
c TRN063 Transient Myeloproliferative Syndrome 17 0.031
937
DFF027 Diffuse Lymphatic Malformation 11 0.031
938
ACC008 Accelerated Tumor Formation 9 0.031
939
FCT015 Factor 2 Deficiency 7 0.031
940
c RNL016 Renal Infectious Disease 7 0.031
941
P HMC003 Hemochromatosis 75 0.029
942
BCK001 Becker Muscular Dystrophy 66 0.029
943
P FCL005 Focal Segmental Glomerulosclerosis 65 0.029
944
c HRD010 Hereditary Spastic Paraplegia 64 0.029
945
CMM004 Common Variable Immunodeficiency 64 0.029
946
P KRT004 Keratitis 63 0.029
947
GTL001 Gitelman Syndrome 63 0.029
948
WRN001 Werner Syndrome 61 0.029
949
CHR012 Chronic Granulomatous Disease 60 0.029
950
P DYS007 Dyskeratosis Congenita 60 0.029
951
c SRC025 Sarcoidosis 1 60 0.029
952
P PLY011 Polycystic Ovary Syndrome 58 0.029
953
P RTH001 Rothmund-Thomson Syndrome 57 0.029
954
TTN003 Tetanus 55 0.029
955
P TXP001 Toxoplasmosis 54 0.029
956
GLL022 Guillain-Barre Syndrome 54 0.029
957
c ATM011 Autoimmune Hepatitis 53 0.029
958
GLB015 Glioblastoma Multiforme 52 0.029
959
c ACT210 Acute Respiratory Distress Syndrome 52 0.029
960
P THR015 Thrombophilia 52 0.029
961
P ICH001 Ichthyosis Vulgaris 51 0.029
962
P GRV001 Graves' Disease 51 0.029
963
P GT001 Gout 51 0.029
964
HYP056 Hypoglycemia 49 0.029
965
TXC005 Toxic Shock Syndrome 49 0.029
966
EDW001 Edwards Syndrome 49 0.029
967
P LYM025 Lymphedema 48 0.029
968
c HPT003 Hepatitis a 47 0.029
969
PLM012 Pulmonary Sarcoidosis 46 0.029
970
FLR002 Filariasis 46 0.029
971
P EPN002 Ependymoma 45 0.029
972
P PRT013 Portal Hypertension 45 0.029
973
EXF001 Exfoliation Syndrome 45 0.029
974
GST045 Gastroenteritis 45 0.029
975
MYX005 Myxoid Liposarcoma 45 0.029
976
ORL005 Oral Candidiasis 44 0.029
977
CLS007 Classic Kaposi Sarcoma 44 0.029
978
ASP003 Aseptic Meningitis 44 0.029
979
ANR040 Aneurysm 43 0.029
980
P DNR001 Duane Retraction Syndrome 43 0.029
981
c HPT007 Hepatitis E 42 0.029
982
CLC006 Calcinosis 42 0.029
983
CDQ001 Cauda Equina Syndrome 40 0.029
984
FSC004 Fasciitis 40 0.029
985
HMG006 Hmg-Coa Lyase Deficiency 40 0.029
986
PRT038 Protein-Energy Malnutrition 40 0.029
987
DDN006 Duodenitis 40 0.029
988
TRP008 Tropical Calcific Pancreatitis 40 0.029
989
c SML016 Small Intestine Cancer 39 0.029
990
HPT014 Hepatorenal Syndrome 39 0.029
991
HDR003 Hidradenitis 38 0.029
992
IMN002 Iminoglycinuria, Digenic 38 0.029
993
P CMP008 Compartment Syndrome 36 0.029
994
CRN246 Cranioosteoarthropathy 36 0.029
995
THR035 Thrombasthenia 36 0.029
996
P PLN008 Peeling Skin Syndrome 36 0.029
997
SPR008 Supratentorial Primitive Neuroectodermal Tumor 35 0.029
998
AST002 Astroblastoma 35 0.029
999
PRT026 Parotitis 35 0.029
1000
EPG003 Epiglottitis 34 0.029
1001
ACT084 Acute Stress Disorder 34 0.029
1002
GRS001 Gerstmann Syndrome 34 0.029
1003
ECT063 Ectodermal Dysplasia 3, Witkop Type 34 0.029
1004
SML008 Small Intestine Lymphoma 33 0.029
1005
P CPL003 Capillary Leak Syndrome 33 0.029
1006
P CHR102 Charcot-Marie-Tooth Neuropathy 33 0.029
1007
SGT001 Sagittal Sinus Thrombosis 32 0.029
1008
PNM003 Pneumatosis Cystoides Intestinalis 32 0.029
1009
LYM045 Lymphocytic Vasculitis 32 0.029
1010
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 32 0.029
1011
EXT035 Extrinsic Cardiomyopathy 31 0.029
1012
c CNG031 Congenital Nervous System Abnormality 28 0.029
1013
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 28 0.029
1014
MDS019 Mediastinal Malignant Lymphoma 27 0.029
1015
MXD032 Mixed Germ Cell Tumor 27 0.029
1016
CRB026 Cerebellar Astrocytoma 26 0.029
1017
FLS001 Fils Syndrome 26 0.029
1018
LVR006 Liver Lymphoma 25 0.029
1019
6MR001 6-Mercaptopurine Sensitivity 23 0.029
1020
MLR007 Male Reproductive System Disease 23 0.029
1021
RCM004 Recombinant 8 Syndrome 21 0.029
1022
LGP003 Logopenic Progressive Aphasia 20 0.029
1023
TRP022 Tropical Pancreatitis 19 0.029
1024
SPN026 Spinal Cord Lymphoma 15 0.029
1025
c PLN016 Peeling Skin Syndrome Type a 13 0.029
1026
c TCL008 T-Cell Lymphoma 1a 11 0.029
1027
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 0.027
1028
MLR004 Malaria 72 0.027
1029
SCK003 Sickle Cell Anemia 71 0.027
1030
P SCL016 Scleroderma 69 0.027
1031
P EHL033 Ehlers-Danlos Syndrome, Classic Type 60 0.027
1032
OMN001 Omenn Syndrome 59 0.027
1033
PYR013 Pyruvate Kinase Deficiency 59 0.027
1034
PRT036 Peritonitis 58 0.027
1035
ACR008 Acrocallosal Syndrome 58 0.027
1036
P BCK002 Beckwith-Wiedemann Syndrome 58 0.027
1037
DNG003 Dengue Disease 57 0.027
1038
P THL005 Thalassemia 56 0.027
1039
P BDD001 Budd-Chiari Syndrome 56 0.027
1040
ARS001 Aarskog-Scott Syndrome 55 0.027
1041
ALP001 Alopecia Universalis 54 0.027
1042
P RHB017 Rhabdoid Tumor 54 0.027
1043
LPP001 Lipoprotein Lipase Deficiency 53 0.027
1044
RPP001 Rapp-Hodgkin Syndrome 53 0.027
1045
c FML108 Familial Breast Cancer 52 0.027
1046
VSC003 Visceral Leishmaniasis 52 0.027
1047
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 52 0.027
1048
GLB001 Gilbert Syndrome 52 0.027
1049
CLF027 Cleft Palate, Isolated 52 0.027
1050
MDD011 Mood Disorder 52 0.027
1051