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

2987 hits were found for 'leukemia'

# ++ Fam MCID Name MIFTS Score
1
MYL006 Myeloid Leukemia 64 6.877
2
LKM002 Leukemia 70 6.673
3
ACT019 Acute Myeloid Leukemia 87 5.929
4
CHR065 Chronic Myeloid Leukemia 67 5.821
5
ACT073 Acute Leukemia 62 5.468
6
ACT020 Acute T Cell Leukemia 59 4.871
7
ACT074 Acute Lymphocytic Leukemia 69 4.844
8
ACT009 Acute Monocytic Leukemia 59 4.771
9
ACT119 Acute Promyelocytic Leukemia 64 4.488
10
CHR090 Chronic Lymphocytic Leukemia 56 4.478
11
MGK001 Megakaryocytic Leukemia 53 4.363
12
JVN004 Juvenile Myelomonocytic Leukemia 53 4.043
13
BCL009 B-Cell Chronic Lymphocytic Leukemia 59 3.960
14
TCL004 T-Cell Leukemia 50 3.934
15
ACT095 Acute Biphenotypic Leukemia 49 3.776
16
NTR003 Natural Killer Cell Leukemia 52 3.749
17
ACT115 Acute Myeloid Leukemia, Adult 49 3.600
18
LYM026 Lymphoblastic Leukemia 49 3.403
19
ADL017 Adult T-Cell Leukemia 47 3.395
20
HRY003 Hairy Cell Leukemia 53 3.352
21
CHR285 Chronic Myelomonocytic Leukemia 53 3.237
22
ACT117 Acute Myelomonocytic Leukemia 58 3.186
23
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 3.053
24
ACT098 Acute Erythroid Leukemia 30 3.044
25
CHL061 Childhood Leukemia 46 2.997
26
ADL052 Adult Acute Lymphocytic Leukemia 45 2.949
27
ACT103 Acute Lymphoblastic Leukemia, Childhood 49 2.919
28
MNC007 Monocytic Leukemia 51 2.886
29
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 16 2.863
30
SBC004 Subacute Myeloid Leukemia 16 2.856
31
LRG008 Large Granular Lymphocyte Leukemia 46 2.850
32
PLS016 Plasma Cell Leukemia 49 2.835
33
PRL017 Prolymphocytic Leukemia 41 2.729
34
BCL005 B Cell Prolymphocytic Leukemia 39 2.718
35
PRC048 Precursor B-Cell Acute Lymphoblastic Leukemia 44 2.692
36
P SYS004 Systemic Mastocytosis 65 2.680
37
LKM005 Leukemia, T-Cell, Chronic 18 2.635
38
CHR286 Chronic Neutrophilic Leukemia 42 2.632
39
LYM067 Lymphoid Leukemia 42 2.621
40
CNT018 Central Nervous System Leukemia 38 2.606
41
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 8 2.562
42
c NNN018 Noonan-Like Syndrome Disorder with or Without Juvenile Myelomonocytic Leukemia 15 2.538
43
LKM004 Leukemia, B-Cell, Chronic 29 2.487
44
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 2.461
45
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 11 2.356
46
SBL003 Subleukemic Leukemia 11 2.347
47
ACT183 Acute Myeloid Leukemia with T Translocation 27 2.302
48
TCL005 T-Cell Prolymphocytic Leukemia 44 2.254
49
P FML083 Familial Platelet Disorder with Associated Myeloid Malignancy 23 2.234
50
TST003 Testicular Leukemia 19 2.206
51
INH015 Inherited Acute Myeloid Leukemia 15 2.198
52
PRG005 Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 11 2.169
53
CHR064 Chronic Monocytic Leukemia 17 2.156
54
PST004 Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 11 2.151
55
NLL001 Null-Cell Leukemia 13 2.127
56
PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 13 2.115
57
ACT113 Acute Myeloblastic Leukemia with Maturation 6 2.112
58
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 9 2.097
59
ACT114 Acute Myeloblastic Leukemia Without Maturation 6 2.093
60
HCL001 Hcl-V 16 2.089
61
MST002 Mast-Cell Leukemia 47 2.050
62
CRB138 Core Binding Factor Acute Myeloid Leukemia 42 2.048
63
ACT140 Acute Undifferentiated Leukemia 33 2.039
64
ACT177 Acute Basophilic Leukemia 32 1.955
65
PRB001 Pre-B-Cell Acute Lymphoblastic Leukemia 36 1.944
66
ALK003 Aleukemic Leukemia Cutis 18 1.924
67
LKM036 Leukemia, Acute Nonlymphocytic 15 1.922
68
P LFR001 Li-Fraumeni Syndrome 75 1.901
69
NNT007 Neonatal Leukemia 29 1.901
70
LKM024 Leukemia/lymphoma, T-Cell 33 1.894
71
PDT026 Pediatric T-Cell Leukemia 10 1.890
72
ACT097 Acute Erythroblastic Leukemia 11 1.868
73
SBC006 Subacute Leukemia 13 1.865
74
RFR002 Refractory Hairy Cell Leukemia 10 1.857
75
PLS003 Plasmacytic Leukemia 11 1.842
76
PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 9 1.838
77
ALK002 Aleukemic Monocytic Leukemia Cutis 8 1.838
78
SBC015 Subacute Monocytic Leukemia 10 1.831
79
BLN016 Bilineal Acute Leukemia 9 1.823
80
PRC009 Precursor T-Lymphoblastic Lymphoma/leukemia Refractory 5 1.791
81
ALK014 Aleukemic Mast Cell Leukemia 8 1.723
82
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 23 1.714
83
ACT116 Acute Myeloid Leukemia, Childhood 11 1.649
84
FML114 Familial Chronic Lymphocytic Leukemia 28 1.641
85
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 24 1.639
86
LKM026 Leukemia, Acute Myeloid, Therapy-Related 14 1.632
87
LKM050 Leukemia, Chronic Lymphocytic 1 12 1.620
88
LKM008 Leukemia, Acute Pre-B-Cell 14 1.614
89
LYM061 Lymphocytic Leukemia, Acute T-Cell 12 1.607
90
c 8P1002 8p11 Myeloproliferative Syndrome 31 1.569
91
ACT118 Acute Non Lymphoblastic Leukemia 24 1.567
92
LKM055 Leukemia, Acute Lymphoblastic 2 11 1.555
93
PRC017 Precursor Lymphoblastic Lymphoma/leukemia 8 1.553
94
HMN022 Human T-Cell Leukemia Virus Type 2 26 1.550
95
LKM057 Leukemia, Post-Chemotherapy 11 1.545
96
HMN021 Human T-Cell Leukemia Virus Type 1 30 1.542
97
ACT106 Acute Myeloblastic Leukemia Type 1 4 1.534
98
LKM016 Leukemia, Acute Myeloid, Somatic 10 1.531
99
ACT107 Acute Myeloblastic Leukemia Type 2 4 1.531
100
LKM056 Leukemia, Chronic Lymphocytic 2 9 1.527
101
ACT108 Acute Myeloblastic Leukemia Type 3 4 1.527
102
CLL014 Cll/sll 19 1.524
103
ACT110 Acute Myeloblastic Leukemia Type 5 4 1.521
104
ACT111 Acute Myeloblastic Leukemia Type 6 4 1.518
105
ACT112 Acute Myeloblastic Leukemia Type 7 4 1.514
106
ACT180 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv or T 10 1.498
107
LKM054 Leukemia, Acute Lymphocytic 1 8 1.498
108
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 7 1.493
109
LKM051 Leukemia, Chronic Lymphocytic 3 6 1.493
110
ACT109 Acute Myeloblastic Leukemia Type 4 3 1.493
111
LKM053 Leukemia, Chronic Lymphocytic 4 7 1.488
112
FML095 Familial Acute Lymphocytic Leukemia 3 1.488
113
LYM062 Lymphoma/leukemia, B-Cell, Variant 7 1.483
114
HMN023 Human T-Cell Leukemia Virus Type 3 3 1.483
115
LKM018 Leukemia, T-Cell Acute Lymphoblastoid 7 1.477
116
LKM052 Leukemia, Chronic Lymphocytic 5 6 1.477
117
SPL013 Splenic Manifestation of Leukemia 6 1.477
118
LKM058 Leukemia, Acute Lymphoblastic, Somatic 5 1.477
119
CHL029 Childhood Precursor T-Lymphoblastic Lymphoma/leukemia 5 1.477
120
NPM001 Npm1-Related Acute Myeloid Leukemia 4 1.477
121
c FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 3 1.477
122
MYL018 Myelocytic Leukemia-Like Syndrome, Familial, Chronic 1 1.477
123
ACT178 Acute Myeloid Leukemia with Multilineage Dysplasia 7 1.470
124
LKM009 Leukemia/lymphoma, B-Cell, 2 5 1.470
125
LKM010 Leukemia/lymphoma, B-Cell, 3 5 1.470
126
LKM017 Leukemia, Acute Myeloid, Reduced Survival in 5 1.470
127
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 3 1.470
128
FML115 Familial Chronic Myelocytic Leukemia 1 1.470
129
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 0 1.470
130
HRY001 Hairy Cell Leukemia of Spleen 8 1.462
131
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 7 1.462
132
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 7 1.462
133
BND002 B- and T-Cell Mixed Leukemia 6 1.462
134
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 6 1.462
135
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 5 1.462
136
LKM020 Leukemia, Acute Myeloid, with Eosinophilia 4 1.462
137
LKM023 Leukemia, Myeloid/lymphoid or Mixed-Lineage 4 1.462
138
MYL050 Myeloid Leukemia, Acute, M4/m4eo Subtype, Somatic 4 1.462
139
TCL013 T-Cell Prolymphocytic Leukemia, Somatic 4 1.462
140
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 3 1.462
141
LKM019 Leukemia, Philadelphia Chromosome-Positive, Resistant to Imatinib 3 1.462
142
LKM022 Leukemia, Acute Promyelocytic, Pml/rara Type 3 1.462
143
LKM034 Leukemia, Transient, of Down Syndrome 3 1.462
144
LKM035 Leukemia, Acute Promyelocytic, Stat5b/rara Type 3 1.462
145
LKM037 Leukemia, Acute Promyelocytic, Numa/rara Type 3 1.462
146
LKM038 Leukemia, Acute Promyelocytic, Npm/rara Type 3 1.462
147
LKM039 Leukemia, Acute Promyelocytic, Pl2f/rara Type 3 1.462
148
SPL002 Splenic Manifestation of Prolymphocytic Leukemia 3 1.462
149
SPL010 Splenic Manifestation of Hairy Cell Leukemia 3 1.462
150
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 2 1.462
151
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 1 1.462
152
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 1 1.462
153
CLS019 Classic Mast Cell Leukemia 0 1.462
154
FML096 Familial Acute Myelocytic Leukemia 0 1.462
155
LYM040 Lymphoblastic Lymphoma 54 1.395
156
NSY001 N Syndrome 57 1.295
157
RCH001 Richter's Syndrome 46 1.232
158
ACT187 Activated Pi3k-Delta Syndrome 12 1.196
159
P HYP098 Hypereosinophilic Syndrome 61 1.187
160
EMB016 Emberger Syndrome 15 1.156
161
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 36 1.149
162
P FML045 Familial Mosaic Monosomy 7 Syndrome 11 1.130
163
DGG001 Di Guglielmo's Syndrome 5 1.124
164
ACT188 Activated Pi3k-Delta Immunodeficiency Syndrome 11 1.100
165
CRB137 Cerebral Creatine Deficiency Syndrome 23 1.089
166
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 14 1.075
167
WTL001 Wt Limb Blood Syndrome 17 1.034
168
END072 Endotheliitis 51 0.348
169
c XP2001 Xp22.3 Microdeletion Syndrome 17 0.319
170
IDP042 Idiopathic Recurrent Stupor 15 0.250
171
P ADL001 Adult Lymphoma 23 0.249
172
14Q004 14q22q23 Microdeletion Syndrome 25 0.248
173
SCD002 Scid, Autosomal Recessive, T-Negative/b-Positive Type 17 0.248
174
3Q2005 3q26q27 Microdeletion Syndrome 14 0.248
175
ANK002 Ankylosing Spondylitis 75 0.225
176
NNN017 Noonan/ Costello/ Leopard/ Cardiofaciocutaneous Syndrome Multi-Gene Panels 11 0.204
177
17Q003 17q11.2 Microduplication Syndrome 21 0.197
178
SCN006 Secondary Syphilis 53 0.195
179
ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 26 0.195
180
BLS007 Blastic Plasmacytoid Dendritic Cell 37 0.194
181
THR013 Thoracic Outlet Syndrome 53 0.190
182
LYM019 Lymphosarcoma 53 0.185
183
ATX002 Ataxia Telangiectasia 81 0.185
184
DWN001 Down Syndrome 58 0.185
185
SVR047 Severe Combined Immunodeficiency Due to Dna-Pkcs Deficiency 14 0.182
186
HMT018 Hematopoietic Stem Cell Transplantation 41 0.179
187
MYL040 Myelodysplastic Syndromes 72 0.176
188
TFT003 Tufting Enteropathy 26 0.169
189
MLN020 Melanoma, Malignant, Somatic 46 0.165
190
21Q001 21q22.11q22.12 Microdeletion Syndrome 13 0.165
191
c MYL007 Myeloma 53 0.163
192
14Q001 14q12 Microdeletion Syndrome 23 0.162
193
c 2P1003 2p13.2 Microdeletion Syndrome 11 0.162
194
PRL042 Proliferating Trichilemmal Cyst 40 0.160
195
c DST058 Distal Monosomy 12p 16 0.157
196
SVR036 Severe Combined Immune Deficiency, Autosomal Recessive T Cell-Negative, B Cell-Positive, Nk Cell-Positive, Il7r-Related 15 0.157
197
MNS013 Monosomy 13q34 14 0.157
198
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 47 0.156
199
SPS019 Spastic Paraparesis 49 0.153
200
SRC014 Sarcoma 54 0.152
201
17Q001 17q21.31 Microdeletion Syndrome 29 0.151
202
MCR071 Microdeletion 15q11.2 21 0.151
203
c MST009 Mastocytosis 67 0.147
204
MYL003 Myeloid Sarcoma 49 0.145
205
SVR020 Severe Combined Immune Deficiency Multi-Gene Panels 10 0.145
206
RFR010 Refractory Anemia 50 0.140
207
SPS077 Sepsis 67 0.139
208
LKS001 Leukostasis 45 0.139
209
IMM068 Immunodeficiency 8 25 0.139
210
c 2Q3005 2q31.1 Microdeletion Syndrome 22 0.139
211
17Q007 17q11 Microdeletion Syndrome 21 0.139
212
c RNG028 Ring Chromosome Y 17 0.138
213
MYC006 Mycosis Fungoides 68 0.137
214
ACN002 Acanthosis Nigricans 70 0.136
215
c CHR226 Chromosome 1q41-Q42 Deletion Syndrome 23 0.136
216
P MLT019 Multiple Myeloma 76 0.135
217
BRN024 Bronchitis 71 0.135
218
c ERL004 Early Yaws 29 0.133
219
12P001 12p12.1 Microdeletion Syndrome 15 0.132
220
c TCL008 T-Cell Lymphoma 1a 13 0.132
221
P GRF002 Graft Versus Host Disease 64 0.131
222
NNS006 Non-Suppurative Otitis Media 24 0.131
223
GRF006 Grfoma 20 0.131
224
c RCR005 Recurrent Fever Multi-Gene Panels 9 0.131
225
HNM001 Hinman's Syndrome 28 0.129
226
ATM010 Autoimmune Hemolytic Anemia 55 0.128
227
CLC008 Colchicine Resistance 28 0.127
228
c ESS003 Essential Thrombocythemia 60 0.127
229
DNT005 Dentatorubral-Pallidoluysian Atrophy 57 0.126
230
PRX003 Paroxysmal Nocturnal Hemoglobinuria 55 0.126
231
DST056 Distal 22q11.2 Microdeletion Syndrome 33 0.126
232
JCB001 Jacobsen Syndrome 49 0.126
233
P MYL005 Myelofibrosis 67 0.123
234
c LCL006 Localized Scleroderma 64 0.123
235
c MYL014 Myeloproliferative Disorder 54 0.123
236
c WLM002 Wilms Tumor 50 0.123
237
P CNG124 Congenital Rubella 51 0.121
238
GLL008 Gilles De La Tourette Syndrome 60 0.120
239
ENT015 Enthesitis-Related Arthritis 50 0.120
240
c 5Q3001 5q35 Microduplication Syndrome 16 0.120
241
SCD001 Scid Due to Lck Deficiency 13 0.120
242
P DFF005 Diffuse Large B-Cell Lymphoma 56 0.119
243
TLY002 T-Lymphocytopenia 42 0.119
244
WST005 West Nile Virus 46 0.118
245
PRX023 Paroxysmal Nocturnal Hemoglobinuria, Somatic 24 0.118
246
c CHR266 Chromosome 8p23.1 Deletion 21 0.118
247
c NTR004 Neutropenia 59 0.118
248
RSD004 Rosai-Dorfman Disease 44 0.117
249
THR004 Thrombocytosis 61 0.116
250
CHL079 Children's Interstitial Lung Disease 39 0.116
251
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 35 0.116
252
BNZ002 Benzene Toxicity 28 0.116
253
10P002 10p11.21p12.31 Microdeletion Syndrome 14 0.116
254
SPR092 Sporadic Pheochromocytoma 36 0.114
255
19Q001 19q13.11 Microdeletion Syndrome 21 0.114
256
P BRS047 Breast Cancer 85 0.113
257
HDG007 Hodgkin's Lymphoma 80 0.113
258
WST001 West Syndrome 64 0.113
259
PRR002 Pure Red-Cell Aplasia 42 0.113
260
BRL003 Bare Lymphocyte Syndrome 36 0.113
261
c XQ1001 Xq12-Q13.3 Duplication Syndrome 10 0.113
262
P NRF002 Neurofibromatosis 86 0.112
263
LNG024 Langerhans-Cell Histiocytosis 63 0.112
264
HPT023 Hepatocellular Carcinoma 69 0.111
265
FNC001 Fanconi's Anemia 66 0.111
266
17Q004 17q12 Microdeletion Syndrome 32 0.111
267
BRN056 Bronchopulmonary Dysplasia 55 0.110
268
SFT003 Soft Tissue Sarcoma 46 0.109
269
BRK003 Burkitt's Lymphoma 71 0.108
270
SPN119 Spondylarthropathy 44 0.107
271
P MLT075 Multifocal Motor Neuropathy 43 0.107
272
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.107
273
c FML139 Familial Myeloma 20 0.107
274
PST046 Post-Transplant Lymphoproliferative Disease 54 0.106
275
PRN029 Parainfluenza Virus Type 3 30 0.106
276
P ESN007 Eosinophilia 54 0.105
277
HML002 Hemolytic Anemia 60 0.104
278
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.104
279
ALL014 Allergic Encephalomyelitis 46 0.104
280
EMN001 Emanuel Syndrome 34 0.104
281
c CHR417 Chronic Graft Versus Host Disease 49 0.103
282
P FLL037 Follicular Lymphoma 47 0.102
283
1P3001 1p36 Deletion Syndrome 44 0.102
284
ENT001 Enterocele 39 0.102
285
12Q001 12q15q21.1 Microdeletion Syndrome 14 0.102
286
HYP004 Hypercalcemia 69 0.102
287
RLP001 Relapsing Polychondritis 66 0.102
288
DSM004 Desmoid Tumor 63 0.102
289
P SPR035 Superior Vena Cava Syndrome 34 0.102
290
17P002 17p13.3 Microduplication Syndrome 26 0.102
291
15Q004 15q11q13 Microduplication Syndrome 19 0.102
292
P UVT001 Uveitis 66 0.100
293
THR035 Thrombasthenia 49 0.100
294
P HST010 Histiocytosis 61 0.099
295
P CHR092 Chronic Myeloproliferative Disease 48 0.099
296
P ANG001 Angelman Syndrome 67 0.099
297
ART019 Aortic Valve Stenosis 64 0.099
298
LKM001 Leukemoid Reaction 44 0.099
299
P HYP117 Hypertriglyceridemia 63 0.098
300
c ACT135 Acute Graft Versus Host Disease 55 0.098
301
FCT013 Factor V Leiden Thrombophilia 31 0.098
302
BRG002 Berger Disease 30 0.098
303
CRK001 Cork-Handlers' Disease 28 0.098
304
FNC043 Fanconi Anemia, Complementation Group E 27 0.098
305
c PRM041 Primary Cortisol Resistance 19 0.098
306
c TTL001 Total Internal Ophthalmoplegia 17 0.098
307
P THY023 Thymoma 63 0.096
308
MLR002 Miliary Tuberculosis 53 0.096
309
P IDP049 Idiopathic Anterior Uveitis 30 0.096
310
TTR011 Tetraploidy 54 0.095
311
c ATX010 Ataxia Neuropathy Spectrum 33 0.095
312
JBR008 Juberg-Hayward Syndrome 21 0.095
313
EGG001 Egg Allergy 43 0.094
314
P SLP004 Salpingo-Oophoritis 30 0.094
315
MLT034 Multicystic Renal Dysplasia, Bilateral 23 0.094
316
P CHR225 Chromosome 1q21.1 Duplication Syndrome 22 0.094
317
c 3Q2004 3q26 Microduplication Syndrome 11 0.094
318
P XRD018 Xeroderma Pigmentosum, Group a 60 0.094
319
c 3Q2003 3q29 Microdeletion Syndrome 37 0.094
320
12Q002 12q14 Microdeletion Syndrome 28 0.094
321
HYP319 Hypereosinophilic Syndrome, Idiopathic, Resistant to Imatinib 27 0.094
322
2Q3003 2q32q33 Microdeletion Syndrome 25 0.094
323
c 2Q2001 2q23.1 Microdeletion Syndrome 25 0.094
324
DMD001 Demodicidosis 17 0.094
325
c MLG054 Malignant Histiocytosis 58 0.093
326
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.093
327
MXL004 Maxillary Sinus Squamous Cell Carcinoma 38 0.093
328
BNM005 Bone Marrow Necrosis 35 0.093
329
SYS011 Systemic Lupus Erythematosus, Association with 28 0.093
330
c LNG057 Long Qt Syndrome 13 17 0.093
331
LNG032 Lung Cancer 61 0.092
332
TRP002 Tropical Spastic Paraparesis 44 0.092
333
P RHM011 Rheumatoid Arthritis 83 0.091
334
P DNS004 Duane Syndrome Type 2 31 0.091
335
XP2002 Xp22.13p22.2 Duplication Syndrome 12 0.091
336
DSS009 Disseminated Intravascular Coagulation 59 0.090
337
CYT008 Cytomegalovirus Infection 50 0.090
338
CRV045 Cervical Intraepithelial Neoplasia 47 0.090
339
HMP002 Hemophagocytic Lymphohistiocytosis 62 0.089
340
HYD012 Hydrops Fetalis 61 0.089
341
P MLN008 Melanoma 56 0.089
342
P THR090 Thrombocythemia 1 48 0.089
343
c ACR001 Aicardi-Goutieres Syndrome 46 0.089
344
DSC009 Discoid Lupus Erythematosus 44 0.089
345
c PRM046 Primary Malignant Lymphoma 43 0.089
346
ACQ031 Acquired Idiopathic Sideroblastic Anemia 25 0.089
347
ADS010 Aids, Slow Progression to 25 0.089
348
c MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 22 0.089
349
SDD005 Sudden Cardiac Death Multi-Gene Panels 19 0.089
350
P RSP003 Respiratory Failure 60 0.088
351
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.088
352
P ART022 Arthritis 75 0.087
353
AND002 Androgen Insensitivity Syndrome 75 0.087
354
c THR014 Thrombocytopenia 66 0.087
355
c HPT021 Hepatitis 65 0.087
356
c AXN002 Axenfeld-Rieger Syndrome 57 0.087
357
INV001 Invasive Aspergillosis 47 0.087
358
OCL020 Ocular Cicatricial Pemphigoid 44 0.087
359
CRY021 Cryoglobulinemic Vasculitis 36 0.087
360
c CHR243 Chromosome 3p Deletion 29 0.087
361
INT206 Intellectual Deficit, X-Linked - Macrocephaly - Macro-Orchidism 11 0.087
362
WDM003 Wiedemann Opitz Syndrome 9 0.087
363
SDR002 Siderosis 50 0.086
364
PLY018 Polycythemia 55 0.086
365
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 16 0.086
366
APL001 Aplastic Anemia 77 0.085
367
P HMP004 Hemophilia B 66 0.085
368
MNT001 Mantle Cell Lymphoma 63 0.085
369
IRN001 Iron Deficiency Anemia 58 0.085
370
MYC002 Mycobacterium Avium Complex Disease 56 0.085
371
EXT010 Extramedullary Plasmacytoma 52 0.085
372
P AVS004 Avascular Necrosis of the Femoral Head 40 0.085
373
P BRD043 Bardet-Biedl Syndrome, Modifier of 36 0.085
374
MYL046 Myelodysplastic Syndrome, Somatic 32 0.085
375
c 4Q2001 4q21 Microdeletion Syndrome 24 0.085
376
PLY001 Polycythemia Vera 77 0.084
377
ABT001 Abetalipoproteinemia 64 0.084
378
PRP030 Purpura 60 0.084
379
c ATX004 Ataxia 56 0.084
380
RTC002 Reticular Dysgenesis 51 0.084
381
LKP003 Leukoplakia 45 0.084
382
IPX001 Ipex Syndrome 35 0.084
383
MNT053 Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations 29 0.084
384
VRS001 Virus Associated Hemophagocytic Syndrome 24 0.084
385
FMR002 Femoral Cancer 22 0.084
386
SVR031 Severe Combined Immunodeficiency, Athabascan Type 19 0.084
387
SVR011 Severe Combined Immunodeficiency, Atypical 18 0.084
388
P NJM001 Nijmegen Breakage Syndrome 69 0.083
389
VSC011 Vasculitis 65 0.083
390
ZYG002 Zygomycosis 38 0.083
391
P PRS040 Prostate Cancer 76 0.082
392
SVR004 Severe Combined Immunodeficiency 75 0.082
393
ASP006 Aspergillosis 68 0.082
394
P PNM007 Pneumonia 67 0.082
395
c PRP029 Porphyria 56 0.082
396
APH001 Aphthous Stomatitis 56 0.082
397
CRT033 Corticobasal Degeneration 53 0.082
398
SPL018 Splenomegaly 50 0.082
399
P ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 34 0.082
400
WDM004 Wiedemann-Steiner Syndrome 20 0.082
401
GNR028 Generalized Essential Telangiectasia 16 0.082
402
DDF001 Dedifferentiated Liposarcoma 48 0.081
403
MLD010 Mild Phenylketonuria 16 0.081
404
SPT013 Septic Shock 62 0.080
405
PLY041 Polymyositis 61 0.080
406
ART001 Arterial Tortuosity Syndrome 52 0.080
407
PCH007 Pouchitis 50 0.080
408
P CNG052 Congenital Amegakaryocytic Thrombocytopenia 45 0.080
409
AND003 Andersen-Tawil Syndrome 39 0.080
410
CTN026 Cutaneous Neuroendocrine Carcinoma 35 0.080
411
HMC004 Homocysteine Plasma Level 31 0.080
412
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 26 0.080
413
ZP7002 Zap-70 Deficiency 20 0.080
414
PRT015 Partial Third-Nerve Palsy 19 0.080
415
SVR042 Severe Combined Immunodeficiency Due to Lck Deficiency 15 0.080
416
c 9P1001 9p13 Microdeletion Syndrome 13 0.080
417
P RTT002 Rett Syndrome 75 0.079
418
MCR004 Macroglobulinemia 54 0.079
419
EPT020 Epithelioid Hemangioendothelioma 51 0.079
420
GLC037 Glucocorticoid Resistance 46 0.079
421
STR077 Streptococcal Toxic-Shock Syndrome 42 0.079
422
RFR008 Refractory Anemia with Excess Blasts 28 0.079
423
HYP179 Hypertrichosis Congenital Generalized X-Linked 18 0.079
424
LJN002 Lujan Syndrome 34 0.078
425
LYM032 Lymphoplasmacytoid Lymphoma 21 0.078
426
RFR011 Refractory Anemia with Excess Blasts-2 10 0.078
427
P ALZ001 Alzheimer's Disease 93 0.077
428
P BCL006 B-Cell Lymphomas 58 0.077
429
P DBT005 Diabetes Insipidus 56 0.077
430
P SVR003 Severe Congenital Neutropenia 55 0.077
431
TBR011 Tuberculous Meningitis 51 0.077
432
c NNN003 Noonan Syndrome 73 0.076
433
LRN002 Laron Syndrome 65 0.076
434
RBR001 Roberts Syndrome 55 0.076
435
SRS001 Serous Cystadenocarcinoma 54 0.076
436
GRY002 Gray Platelet Syndrome 51 0.076
437
TRP014 Triploidy 46 0.076
438
c HPT073 Hepatitis C Virus 43 0.076
439
CLR034 Colorectal Cancer, Somatic 41 0.076
440
P THR045 Thrombotic Thrombocytopenic Purpura, Congenital 35 0.076
441
END017 Endocardium Cancer 16 0.076
442
P ISC010 Isochromosome Yp 14 0.076
443
CYT018 Cytochrome P450 2d6 Variant 12 0.076
444
P WLD002 Waldenstrom Macroglobulinemia 52 0.075
445
c KBK001 Kabuki Syndrome 47 0.075
446
JVN033 Juvenile Nasopharyngeal Angiofibroma 46 0.075
447
c FML024 Familial Melanoma 45 0.075
448
c XRD012 Xeroderma Pigmentosum, Group D 41 0.075
449
P HRD018 Hair Disease 33 0.075
450
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 32 0.075
451
P HPT001 Hepatitis C 66 0.074
452
P CRT049 Critical Limb Ischemia 58 0.074
453
P PNC001 Pancytopenia 55 0.074
454
VNS010 Venous Thromboembolism 54 0.074
455
OST081 Osteoporosis, Postmenopausal 47 0.074
456
c RSM001 Rasmussen Encephalitis 46 0.074
457
IMM054 Immunoproliferative Small Intestinal Disease 31 0.074
458
CLN016 Colon Cancer 66 0.072
459
ATM004 Autoimmune Thrombocytopenic Purpura 62 0.072
460
SQM006 Squamous Cell Carcinoma 58 0.072
461
HMN016 Hemangioendothelioma 51 0.072
462
EVN001 Evans' Syndrome 50 0.072
463
UTR043 Uterine Sarcoma 50 0.072
464
c PRG060 Pregnancy Loss 48 0.072
465
CRB009 Cerebritis 46 0.072
466
TLN003 Telangiectasis 46 0.072
467
HST016 Histiocytic Sarcoma 43 0.072
468
PRP016 Paraplegia 42 0.072
469
ICH002 Ichthyosis Bullosa of Siemens 41 0.072
470
LYM045 Lymphocytic Vasculitis 38 0.072
471
15Q001 15q13.3 Microdeletion 29 0.072
472
ZP7001 Zap70-Related Severe Combined Immunodeficiency 24 0.072
473
16Q001 16q24.3 Microdeletion Syndrome 23 0.072
474
HRD009 Hereditary Wilms' Tumor 19 0.072
475
SVR022 Severe Combined Immune Deficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive, Rag1/rag2-Related 15 0.072
476
ACQ007 Acquired Immunodeficiency Syndrome 62 0.071
477
GMM002 Gamma Chain Deficiency 54 0.071
478
MDS022 Mediastinitis 49 0.071
479
STN007 Stenotrophomonas Maltophilia 46 0.071
480
BCK006 Back Pain 46 0.071
481
ANP009 Anaplastic Oligodendroglioma 44 0.071
482
P END033 Endocarditis 42 0.071
483
CHR276 Chronic Active Epstein-Barr Virus Infection 42 0.071
484
DXR001 Doxorubicin Induced Cardiomyopathy 38 0.071
485
INT038 Interdigitating Dendritic Cell Sarcoma 34 0.071
486
XLN005 X-Linked Hyper Igm Syndrome 31 0.071
487
NRG004 Neurogenic Diabetes Insipidus 31 0.071
488
CRB132 Cerebral Sinovenous Thrombosis 30 0.071
489
BLD087 Bladder Cancer, Somatic 24 0.071
490
HYP439 Hyperammonemia Multi-Gene Panels 9 0.071
491
PRM132 Primary Cutaneous Cd4+ Small/medium-Sized Pleomorphic T-Cell Lymphoma 7 0.071
492
c MNN013 Meningitis 62 0.070
493
DPH001 Diphtheria 54 0.070
494
NRP001 Neuropathy 54 0.070
495
BCT015 Bacteremia 52 0.070
496
P ALV004 Alveolar Rhabdomyosarcoma 51 0.070
497
P SVR013 Severe Congenital Neutropenia Autosomal Recessive 3 23 0.070
498
ART109 Arterial Thoracic Outlet Syndrome 17 0.070
499
P RTN024 Retinoblastoma 70 0.069
500
P LPR002 Leopard Syndrome 66 0.069
501
DFC004 Deficiency Anemia 65 0.069
502
c CWD001 Cowden Disease 63 0.069
503
HYP266 Hypoxia 60 0.069
504
HMT002 Hematologic Cancer 56 0.069
505
NRF007 Neurofibroma 51 0.069
506
c PST005 Posterior Uveitis 49 0.069
507
RCR001 Recurrent Corneal Erosion 43 0.069
508
c ANT034 Anterior Uveitis 42 0.069
509
SPR005 Superficial Basal Cell Carcinoma 39 0.069
510
GNT031 Genitopatellar Syndrome 39 0.069
511
LYM105 Lymphoma, Follicular, Somatic 35 0.069
512
CHR020 Chronic Interstitial Cystitis 35 0.069
513
P SRC025 Sarcoidosis 1 30 0.069
514
MLG083 Male Germ Cell Tumor 29 0.069
515
JVN024 Juvenile Hereditary Hemochromatosis 28 0.069
516
MLN045 Melanoma of Soft Part 28 0.069
517
FTL044 Fetal Cytomegalovirus Syndrome 22 0.069
518
c CHR224 Chromosome 1q Duplication 20 0.069
519
16P004 16p13.11 Microduplication Syndrome 15 0.069
520
P INS005 Insulin Resistance 62 0.068
521
P GLM007 Glomerulonephritis 60 0.068
522
CLL003 Cellulitis 53 0.068
523
PYD001 Pyoderma Gangrenosum 53 0.068
524
FML089 Familial Thoracic Aortic Aneurysm and Dissection 39 0.068
525
DYS036 Dysequilibrium Syndrome 32 0.068
526
MMR004 Memory Impairment 52 0.067
527
MCS003 Mucous Membrane Pemphigoid 51 0.067
528
ADL002 Adult Syndrome 50 0.067
529
NRP002 Neuroepithelioma 49 0.067
530
ADS004 Aids Dementia Complex 47 0.067
531
PNM013 Pneumococcal Meningitis 47 0.067
532
FML055 Familial Cylindromatosis 38 0.067
533
c UNL002 Unilateral Retinoblastoma 32 0.067
534
MND001 Mandibular Cancer 26 0.067
535
MLR006 Male Reproductive Organ Cancer 21 0.067
536
P XQ2001 Xq27.3q28 Duplication Syndrome 21 0.067
537
17Q006 17q21.31 Microduplication Syndrome 18 0.067
538
RFR007 Refractory Anemia with Excess Blasts in Transformation 13 0.067
539
c MNS014 Monosomy 22 12 0.067
540
SMT015 Smith Magenis Syndrome 58 0.066
541
FLT001 Felty's Syndrome 54 0.066
542
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.066
543
PRN001 Purine Nucleoside Phosphorylase Deficiency 52 0.066
544
NPH018 Nephrogenic Systemic Fibrosis 50 0.066
545
PYM001 Pyomyositis 44 0.066
546
HYP030 Hypoactive Sexual Desire Disorder 39 0.066
547
CHR055 Chordoid Meningioma 38 0.066
548
GNR023 Generalized Eruptive Histiocytosis 16 0.066
549
P INF038 Influenza 63 0.064
550
VNS009 Venous Thrombosis 56 0.064
551
P CND004 Candidiasis 55 0.064
552
HYP063 Hypersplenism 52 0.064
553
P PND001 Pain Disorder 49 0.064
554
CHL056 Cheilitis 49 0.064
555
c CPL003 Capillary Leak Syndrome 44 0.064
556
ADN064 Adenohypophysitis 42 0.064
557
DNR001 Duane Retraction Syndrome 41 0.064
558
c MLG088 Malignant Germ Cell Tumor 35 0.064
559
ACT167 Acute Generalized Exanthematous Pustulosis 33 0.064
560
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 33 0.064
561
c ATX025 Ataxia, Spastic, 5, Autosomal Recessive 14 0.064
562
ALP006 Alpha Thalassemia 68 0.063
563
URT039 Urticaria 61 0.063
564
P NRB001 Neuroblastoma 60 0.063
565
P HRP006 Herpes Simplex 57 0.063
566
STR008 Strongyloidiasis 55 0.063
567
P PLM006 Pulmonary Alveolar Proteinosis 55 0.063
568
APP008 Appendicitis 54 0.063
569
DBT004 Diabetic Polyneuropathy 52 0.063
570
c ALM001 Al Amyloidosis 49 0.063
571
GRN017 Granulocytopenia 41 0.063
572
P BNL002 Bone Lymphoma 31 0.063
573
MLG041 Malignant Triton Tumor 28 0.063
574
BLT011 Bilateral Perisylvian Polymicrogyria 25 0.063
575
5FL001 5-Fluorouracil Toxicity 23 0.063
576
NRL016 Neural Tube Defects 69 0.062
577
P PRP003 Porphyria Cutanea Tarda 68 0.062
578
TRC032 Turcot Syndrome 66 0.062
579
CHR066 Chronic Fatigue Syndrome 63 0.062
580
P ADN016 Adenocarcinoma 60 0.062
581
ADN011 Adenoid Cystic Carcinoma 56 0.062
582
GRW007 Growth Hormone Deficiency 52 0.062
583
DRM004 Dermatofibrosarcoma 51 0.062
584
INT054 Intraocular Lymphoma 50 0.062
585
SPL004 Splenic Marginal Zone Lymphoma 48 0.062
586
SDR003 Sideroblastic Anemia 44 0.062
587
PRS008 Prostate Small Cell Carcinoma 41 0.062
588
INT103 Intrauterine Infections 41 0.062
589
LPT005 Leptin Deficiency 40 0.062
590
PDT021 Pediatric Osteosarcoma 39 0.062
591
HTL002 Htlv-1 Associated Myelopathy 36 0.062
592
VTM002 Vitamin B12 Deficiency 35 0.062
593
VND002 Van Der Woude Syndrome 34 0.062
594
LYL001 Lyell Syndrome 33 0.062
595
P RNG004 Ring Chromosome 1 31 0.062
596
c SNS011 Sinus Cancer 30 0.062
597
HMG015 Hemoglobin S Beta-Thalassemia 30 0.062
598
GLM037 Glioma Somatic 27 0.062
599
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 21 0.062
600
c DYS055 Dystonia 10 17 0.062
601
SPR021 Supraglottis Cancer 17 0.062
602
MTH028 Mthfr Thermolabile Variant 17 0.062
603
c BNG076 Benign Exophthalmos Syndrome 17 0.062
604
c 8P2001 8p23.1 Microduplication Syndrome 15 0.062
605
ALK017 Alk-Positive Large B-Cell Lymphoma 15 0.062
606
SML025 Small Non-Cleaved Cell Lymphoma 14 0.062
607
c 5Q3002 5q31.3 Microdeletion Syndrome 13 0.062
608
HYP570 Hypothalamic Insufficiency-Secondary Microcephaly-Visual Impairment-Urinary Anomalies 10 0.062
609
20Q002 20q11.2 Microduplication Syndrome 9 0.062
610
P MYS003 Myasthenia Gravis 71 0.060
611
PRT011 Protein C Deficiency 59 0.060
612
c NPH012 Nephrotic Syndrome 57 0.060
613
CNV002 Conversion Disorder 48 0.060
614
BSL011 Basal Cell Carcinoma, Multiple 21 0.060
615
3Q2002 3q21q26 Syndrome 20 0.060
616
P PNC035 Pancreatic Cancer 82 0.059
617
P ADL010 Adult Respiratory Distress Syndrome 66 0.059
618
P ATM006 Autoimmune Lymphoproliferative Syndrome 60 0.059
619
LPS007 Lupus Nephritis 55 0.059
620
PLS011 Plasmacytoma 52 0.059
621
HMG002 Hemoglobinuria 52 0.059
622
ATP002 Atopy 52 0.059
623
GST027 Gastric Lymphoma 51 0.059
624
FNC044 Fanconi Anemia, Complementation Group C 51 0.059
625
MYL001 Myelitis 51 0.059
626
P LMB024 Limbic Encephalitis 47 0.059
627
PRP034 Purpura Fulminans 46 0.059
628
MHC002 Mhc Class I Deficiency 36 0.059
629
BRR002 Barrett's Adenocarcinoma 36 0.059
630
ADS002 Adie Syndrome 32 0.059
631
IMM062 Immunodeficiency 11 25 0.059
632
6Q1001 6q16 Deletion Syndrome 24 0.059
633
HYP084 Hypopyon 23 0.059
634
ECT003 Ectopic Thymus 21 0.059
635
SVR038 Severe Combined Immune Deficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive, Cd3d-Related 15 0.059
636
21Q002 21q22.13q22.2 Microdeletion Syndrome 14 0.059
637
P MLT020 Multiple Sclerosis 75 0.058
638
PMP001 Pemphigus 60 0.058
639
DRM014 Dermatofibrosarcoma Protuberans 59 0.058
640
NNH001 Non-Hodgkin Lymphoma 58 0.058
641
c CNT035 Central Nervous System Disease 52 0.058
642
CNG008 Congenital Ichthyosiform Erythroderma 51 0.058
643
DSM007 Desmoplastic Small Round Cell Tumor 51 0.058
644
CRD001 Cardiac Tamponade 51 0.058
645
CRS001 Crescentic Glomerulonephritis 50 0.058
646
P CLC001 Calciphylaxis 49 0.058
647
NDL013 Nodular Regenerative Hyperplasia 49 0.058
648
c ERY013 Erythrocytosis 48 0.058
649
PLM070 Pulmonic Stenosis 48 0.058
650
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.058
651
PLY100 Polyploidy 45 0.058
652
PLS025 Plasmablastic Lymphoma 45 0.058
653
PRM163 Primary Mediastinal Large B-Cell Lymphoma 44 0.058
654
P PST022 Posterior Uveal Melanoma 44 0.058
655
PYD002 Pyoderma 43 0.058
656
ALP014 Alpha-Thalassemia/mental Retardation Syndrome 42 0.058
657
CRY001 Cryptogenic Organizing Pneumonia 41 0.058
658
URT008 Urticaria Pigmentosa 40 0.058
659
RPP001 Rapp-Hodgkin Syndrome 37 0.058
660
MNC006 Monoclonal Gammopathy of Uncertain Significance 34 0.058
661
P EWN002 Ewing's Family of Tumors 32 0.058
662
RNL065 Renal Cell Carcinoma, Papillary, 1 27 0.058
663
INT029 Interleukin-7 Receptor Alpha Deficiency 26 0.058
664
DND015 Dendritic Cell, Monocyte, B Lymphocyte, and Natural Killer Lymphocyte Deficiency 17 0.058
665
TRS012 Trisomy 22 16 0.058
666
MTR030 Mitral Valve Prolapse, Familial, X-Linked 10 0.058
667
TBR010 Tuberculosis 82 0.056
668
THL005 Thalassemia 69 0.056
669
P FRD001 Friedreich Ataxia 64 0.056
670
ADN001 Adenosine Deaminase Deficiency 63 0.056
671
ADL030 Adult-Onset Still's Disease 61 0.056
672
OCC006 Occipital Horn Syndrome 57 0.056
673
EXT034 Extrinsic Allergic Alveolitis 55 0.056
674
c SBC007 Subacute Thyroiditis 55 0.056
675
INT146 Intervertebral Disc Disease 50 0.056
676
LKP004 Leukopenia 46 0.056
677
PRP023 Peripheral Neuropathy 46 0.056
678
HMC014 Homocysteinemia 46 0.056
679
FLL013 Follicular Dendritic Cell Sarcoma 45 0.056
680
PRN049 Paraneoplastic Pemphigus 43 0.056
681
PSD002 Pseudotumor Cerebri 43 0.056
682
PST055 Postural Hypotension 42 0.056
683
PLM019 Pleomorphic Liposarcoma 42 0.056
684
RHM014 Rheumatoid Vasculitis 41 0.056
685
CLS008 Clostridium Difficile 40 0.056
686
OLG006 Oligoastrocytoma 39 0.056
687
c CHR208 Chromosome 17p Deletion 36 0.056
688
BLD054 Blood Protein Disease 35 0.056
689
PLS009 Plasma Cell Neoplasm 34 0.056
690
MTR001 Mature Cataract 32 0.056
691
ABL001 Ablepharon Macrostomia Syndrome 27 0.056
692
GRF001 Graft-Versus-Host Disease, Protection Against 26 0.056
693
HMG012 Hemoglobin Constant Spring 24 0.056
694
MNS009 Monosomy 13q14 22 0.056
695
CHR176 Chromophil Renal Cell Carcinoma 20 0.056
696
CHL109 Childhood Apraxia of Speech 19 0.056
697
OST085 Osteosarcoma, Somatic 19 0.056
698
c 5P1001 5p13 Microduplication Syndrome 17 0.056
699
NNN007 Non-Involuting Congenital Hemangioma 14 0.056
700
PLL001 Pallister-Hall Syndrome 64 0.055
701
DRM006 Dermatitis 60 0.055
702
c HPT003 Hepatitis a 57 0.055
703
P ANP001 Anaplastic Large Cell Lymphoma 56 0.055
704
P LPS002 Liposarcoma 54 0.055
705
HML001 Hemolytic-Uremic Syndrome 52 0.055
706
CRY005 Cryptococcosis 51 0.055
707
IDP064 Idiopathic Neutropenia 51 0.055
708
RNL014 Renal Cell Carcinoma 51 0.055
709
P PTT014 Pitt-Hopkins Syndrome 49 0.055
710
THY009 Thyroid Lymphoma 48 0.055
711
MNN014 Mononeuritis 40 0.055
712
MHC001 Mhc Class Ii Deficiency 32 0.055
713
c CHR253 Chromosome 5q Deletion 31 0.055
714
c LNG056 Long Qt Syndrome 12 17 0.055
715
PCK001 Pick's Disease 68 0.054
716
GLN003 Glanzmann's Thrombasthenia 68 0.054
717
P MNN012 Meningioma 67 0.054
718
LCH002 Lichen Planus 61 0.054
719
c SRC013 Sarcoidosis 60 0.054
720
HMR012 Hemorrhagic Fever 58 0.054
721
P MMB002 Membranous Glomerulonephritis 56 0.054
722
P PLY019 Polyneuropathy 54 0.054
723
GNR017 Generalized Pustular Psoriasis 51 0.054
724
MYL020 Myelomeningocele 51 0.054
725
PLY013 Polymyalgia Rheumatica 51 0.054
726
P MLG002 Malignant Peritoneal Mesothelioma 51 0.054
727
NNL002 Nonalcoholic Steatohepatitis 50 0.054
728
BSL006 Basaloid Squamous Cell Carcinoma 49 0.054
729
PLM020 Pleomorphic Xanthoastrocytoma 48 0.054
730
HRD004 Hereditary Breast Ovarian Cancer 48 0.054
731
PLM009 Pleomorphic Adenoma Carcinoma 47 0.054
732
CMB021 Combined Pituitary Hormone Deficiency 46 0.054
733
MYX013 Myxofibrosarcoma 45 0.054
734
P MBS002 Moebius Syndrome 45 0.054
735
ACT093 Actinic Cheilitis 43 0.054
736
P CRV039 Cervicitis 41 0.054
737
DFF016 Diffuse Astrocytoma 41 0.054
738
PHY007 Phyllode Tumor 41 0.054
739
RTC005 Reticulosarcoma 40 0.054
740
PRM012 Primary Polycythemia 39 0.054
741
DBL002 Double Outlet Right Ventricle 36 0.054
742
PLM071 Pulmonary Surfactant Metabolism Dysfunction 25 0.054
743
BLD122 Bleeding Disorder, Platelet-Type, 16, Autosomal Dominant 23 0.054
744
HRD111 Hereditary Persistence of Fetal Hemoglobin - Sickle Cell Disease 20 0.054
745
P 19P001 19p13.12 Microdeletion Syndrome 19 0.054
746
BCL003 B-Cell Lymphocytic Neoplasm 18 0.054
747
c KNB001 Knobloch Syndrome 17 0.054
748
17Q005 17q12 Microduplication Syndrome 17 0.054
749
c 2Q3006 2q31.1 Microduplication Syndrome 10 0.054
750
BLM001 Bloom Syndrome 74 0.052
751
BLD042 Bladder Carcinoma 70 0.052
752
c LPS004 Lupus Erythematosus 65 0.052
753
MYS005 Myositis 61 0.052
754
TNS005 Tonsillitis 57 0.052
755
RTN003 Retinal Ischemia 52 0.052
756
OLF005 Olfactory Neuroblastoma 52 0.052
757
P EXN002 Exanthem 50 0.052
758
LYM052 Lymphomatoid Papulosis 50 0.052
759
OST003 Osteonecrosis 49 0.052
760
c SPN183 Spontaneous Pneumothorax 44 0.052
761
CLL013 Cell Type Cancer 42 0.052
762
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 29 0.052
763
PDT001 Pediatric Lymphoma 23 0.052
764
AND005 Androgen Insensitivity Syndrome, Mild 19 0.052
765
OKT001 Okt4 Epitope Deficiency 19 0.052
766
P HYP075 Hypertension 76 0.050
767
KLN001 Klinefelter's Syndrome 66 0.050
768
NPH007 Nephrogenic Diabetes Insipidus 65 0.050
769
c THY032 Thyroiditis 61 0.050
770
CRY004 Cryoglobulinemia 59 0.050
771
P SYN007 Synovitis 58 0.050
772
CCT002 Cicatricial Pemphigoid 58 0.050
773
c ACT134 Acute Liver Failure 55 0.050
774
PRT002 Paratyphoid Fever 55 0.050
775
P CNT005 Central Nervous System Lymphoma 53 0.050
776
PYG006 Pyogenic Granuloma 52 0.050
777
P NRV007 Nervous System Disease 51 0.050
778
OST028 Osteochondroma 49 0.050
779
PRC013 Pericarditis 48 0.050
780
RHB003 Rhabdomyosarcoma 48 0.050
781
WBR001 Weber Syndrome 47 0.050
782
PRC012 Pericardial Effusion 47 0.050
783
MCR191 Microscopic Colitis 46 0.050
784
RHY001 Rhyns Syndrome 45 0.050
785
P JBR004 Joubert Syndrome 2 45 0.050
786
CYC004 Cyclic Hematopoiesis 45 0.050
787
VLV044 Vulvar Intraepithelial Neoplasia 45 0.050
788
GST014 Gastrointestinal Lymphoma 44 0.050
789
HPT032 Hepatocellular Carcinoma, Somatic 43 0.050
790
CHR101 Char Syndrome 42 0.050
791
ETH009 Ethmoid Sinusitis 40 0.050
792
MCR020 Microsporidiosis 39 0.050
793
CHR370 Chronic Granulomatous Disease, Autosomal, Due to Deficiency of Cyba 38 0.050
794
P TST015 Testicular Disease 38 0.050
795
P CTN015 Cutaneous T Cell Lymphoma 37 0.050
796
TST021 Testicular Germ Cell Tumor 34 0.050
797
PRT082 Preterm Premature Rupture of the Membranes 33 0.050
798
MYC018 Mycobacterium Malmoense 30 0.050
799
CD4001 Cd45 Deficiency 28 0.050
800
HVD003 Hiv/aids 27 0.050
801
CNG101 Congenital Human Immunodeficiency Virus 24 0.050
802
c CHR209 Chromosome 17p Duplication 24 0.050
803
ORB012 Orbital Cancer 24 0.050
804
c CHR193 Chromosome 13q Deletion 23 0.050
805
FSR001 Fusariosis 22 0.050
806
c MYL015 Myeloproliferative Disorder with Eosinophilia 15 0.050
807
P PRK066 Parkinsonism with Spasticity, X-Linked 13 0.050
808
P SYS001 Systemic Lupus Erythematosus 83 0.049
809
P GST019 Gastrointestinal Stromal Tumor 75 0.049
810
BTT002 Beta Thalassemia 69 0.049
811
c DBT009 Diabetes Mellitus 68 0.049
812
P RBN001 Rubinstein-Taybi Syndrome 68 0.049
813
P BCK002 Beckwith-Wiedemann Syndrome 62 0.049
814
HYP066 Hyperglycemia 59 0.049
815
CRM001 Crimean-Congo Hemorrhagic Fever 58 0.049
816
HPR003 Heparin-Induced Thrombocytopenia 55 0.049
817
c MCP010 Mucopolysaccharidosis 55 0.049
818
THY089 Thymic Epithelial Neoplasm 53 0.049
819
MLT006 Multidrug-Resistant Tuberculosis 51 0.049
820
P RPD001 Rapidly Progressive Glomerulonephritis 51 0.049
821
PGM001 Pigmented Villonodular Synovitis 51 0.049
822
LPC002 Lip Cancer 50 0.049
823
SPN035 Spindle Cell Sarcoma 50 0.049
824
P CTN014 Cutaneous Mastocytosis 49 0.049
825
c OST019 Osteosclerosis 48 0.049
826
INF058 Inflammatory Myofibroblastic Tumor 47 0.049
827
PNN001 Panniculitis 47 0.049
828
CRN030 Coronary Stenosis 47 0.049
829
P JVN003 Juvenile Xanthogranuloma 46 0.049
830
c ACQ014 Acquired Hemophilia 45 0.049
831
ADN027 Adenomyosis 44 0.049
832
INT221 Intravascular Large B-Cell Lymphoma 44 0.049
833
ACN014 Acanthocytosis 43 0.049
834
ANG046 Angioimmunoblastic T-Cell Lymphoma 42 0.049
835
SPN006 Spindle Cell Lipoma 40 0.049
836
BNM001 Bone Marrow Cancer 38 0.049
837
NM001 Noma 37 0.049
838
PNS012 Paine Syndrome 35 0.049
839
HRD024 Hereditary Persistence of Fetal Hemoglobin 35 0.049
840
FLL019 Follicular Mucinosis 33 0.049
841
MRK002 Marek Disease 31 0.049
842
MLD011 Mild Hyperphenylalaninemia 30 0.049
843
EXT051 Extraskeletal Ewing Sarcoma 28 0.049
844
IDP033 Idiopathic Edema 28 0.049
845
TYP024 Type Ii Mixed Cryoglobulinemia 28 0.049
846
c MLG036 Malignant Spiradenoma 25 0.049
847
DFN039 Deafness-Infertility Syndrome 24 0.049
848
HDG009 Hodgkin Lymphoma, Childhood 23 0.049
849
CYT017 Cytophagic Histiocytic Panniculitis 22 0.049
850
ANP010 Anaplastic Plasmacytoma 17 0.049
851
P AMY001 Amyotrophic Lateral Sclerosis 87 0.047
852
P OBS005 Obesity 79 0.047
853
SCK003 Sickle Cell Anemia 67 0.047
854
P ATM003 Autoimmune Thyroiditis 66 0.047
855
DBT011 Diabetic Retinopathy 66 0.047
856
THR079 Thromboembolism 63 0.047
857
HRP004 Herpes Zoster 60 0.047
858
LKC001 Leukocyte Adhesion Deficiency 60 0.047
859
P MLG075 Malignant Mesothelioma 58 0.047
860
c PNC044 Pancreatitis 58 0.047
861
P OLG002 Oligodendroglioma 56 0.047
862
THR009 Thrombocytopenia-Absent Radius Syndrome 55 0.047
863
GLL031 Guillain-Barr´┐Ż Syndrome 54 0.047
864
P OMP004 Omphalocele 53 0.047
865
c AFB001 Afibrinogenemia 52 0.047
866
CYT005 Cytomegalovirus Retinitis 52 0.047
867
LYM021 Lymphadenitis 50 0.047
868
MCR037 Macroglossia 49 0.047
869
P SLV002 Salivary Gland Cancer 48 0.047
870
HYP025 Hyperphosphatemia 48 0.047
871
LDP002 Lead Poisoning 47 0.047
872
DFF024 Diffuse Panbronchiolitis 44 0.047
873
LCT001 Lactic Acidosis 44 0.047
874
LNG017 Lung Giant Cell Carcinoma 43 0.047
875
CLN015 Colon Adenocarcinoma 41 0.047
876
THL010 Thalassemia Minor 40 0.047
877
WTH001 Withdrawal Disorder 40 0.047
878
c OVR069 Ovarian Germ Cell Tumor 40 0.047
879
ATX019 Ataxia with Vitamin E Deficiency 40 0.047
880
MSC006 Muscle Glycogenosis 39 0.047
881
P OLG015 Oligoarticular Juvenile Arthritis 37 0.047
882
SPL006 Splenic Infarction 36 0.047
883
HMG021 Hemoglobin E - Beta-Thalassemia 34 0.047
884
ICH020 Ichthyosis Prematurity Syndrome 34 0.047
885
LWR010 Low Renin Hypertension 34 0.047
886
IMR001 Imerslund-Grasbeck Syndrome 31 0.047
887
IMM020 Immunodeficiency with Hyper Igm Type 2 29 0.047
888
ENG004 Engraftment Syndrome 28 0.047
889
c HMP017 Hemophilia a, Congenital 26 0.047
890
c LYM063 Lymphoma, Diffuse Large Cell 26 0.047
891
HPT070 Hepatosplenic T-Cell Lymphoma 24 0.047
892
c MNS008 Monosomy 21 22 0.047
893
THP001 Thiopurine S Methyltranferase Deficiency 20 0.047
894
RNL048 Renal Tubular Acidosis, Distal, Type 3 19 0.047
895
c TTR021 Tetrasomy 21 14 0.047
896
AGR001 Age Related Macular Degeneration 71 0.045
897
P CLR023 Colorectal Cancer 66 0.045
898
BRN028 Brain Cancer 65 0.045
899
P RTH001 Rothmund-Thomson Syndrome 63 0.045
900
P LVR013 Liver Disease 62 0.045
901
OMN001 Omenn Syndrome 60 0.045
902
HMH002 Hemihypertrophy 57 0.045
903
GNG013 Gingivitis 56 0.045
904
P NNN008 Noonan Syndrome 1 56 0.045
905
CRC006 Carcinoid Syndrome 55 0.045
906
RTN023 Retinitis 53 0.045
907
P MMB001 Membranoproliferative Glomerulonephritis 52 0.045
908
LYM027 Lymphopenia 51 0.045
909
P PRT039 Proteinuria 51 0.045
910
ACT105 Acute Mountain Sickness 50 0.045
911
c PRL003 Proliferative Glomerulonephritis 49 0.045
912
BRN018 Borna Disease 49 0.045
913
PRP036 Peripheral T-Cell Lymphoma 47 0.045
914
PRM097 Primary Immunodeficiency Disease 46 0.045
915
P CRN074 Coronary Artery Aneurysm 45 0.045
916
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.045
917
DND002 Dendritic Cell Sarcoma 43 0.045
918
MRG003 Marginal Zone B-Cell Lymphoma 43 0.045
919
c LNG063 Lung Cancer Susceptibility 42 0.045
920
TLY001 T Lymphocyte Deficiency 38 0.045
921
PTY004 Pityriasis Lichenoides 34 0.045
922
PLY039 Polymorphic Reticulosis 22 0.045
923
EXF003 Exfoliative Dermatitis 21 0.045
924
INT229 Intellectual Disability-Brachydactyly-Pierre Robin Syndrome 8 0.045
925
P MYC007 Myocardial Infarction 82 0.044
926
ULC004 Ulcerative Colitis 71 0.044
927
P AMY004 Amyloidosis 65 0.044
928
SKN016 Skin Disease 64 0.044
929
PRC016 Pre-Eclampsia 64 0.044
930
PRT010 Parathyroid Carcinoma 63 0.044
931
P STM004 Stomach Cancer 62 0.044
932
c ACT027 Acute Pancreatitis 60 0.044
933
P HRD011 Hereditary Spherocytosis 59 0.044
934
GLB015 Glioblastoma Multiforme 57 0.044
935
MLL005 Miller-Dieker Syndrome 57 0.044
936
c MLR021 Malaria, Severe 56 0.044
937
KDN017 Kidney Cancer 56 0.044
938
GYN001 Gynecomastia 56 0.044
939
HPT022 Hepatoblastoma 56 0.044
940
SLT008 Solitary Fibrous Tumor 55 0.044
941
EPD006 Epidermolysis Bullosa Acquisita 55 0.044
942
THR012 Thoracic Cancer 54 0.044
943
P BRN009 Burning Mouth Syndrome 54 0.044
944
P SNS014 Sinusitis 54 0.044
945
c TRT010 Teratoma 53 0.044
946
RSC001 Rosacea 53 0.044
947
ADN009 Adenosquamous Carcinoma 53 0.044
948
HYP017 Hypophosphatemia 52 0.044
949
FML026 Familial Lipoprotein Lipase Deficiency 50 0.044
950
ART008 Arteriosclerosis Obliterans 50 0.044
951
TXC012 Toxic Epidermal Necrolysis 49 0.044
952
NCR004 Nocardiosis 49 0.044
953
PST010 Pasteurellosis 47 0.044
954
FRZ001 Frozen Shoulder 45 0.044
955
c BNG032 Benign Mesothelioma 45 0.044
956
GLN002 Glanders 44 0.044
957
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 44 0.044
958
CNG027 Congenital Hemolytic Anemia 43 0.044
959
LYM051 Lymphomatoid Granulomatosis 43 0.044
960
WRT003 Warthin Tumor 42 0.044
961
KRT002 Keratomalacia 42 0.044
962
MST001 Mast-Cell Sarcoma 42 0.044
963
LBL001 Lobular Neoplasia 41 0.044
964
SML009 Small Intestine Adenocarcinoma 41 0.044
965
P MLG081 Malignant Teratoma 40 0.044
966
MTG002 Mutagen Sensitivity 40 0.044
967
c ART070 Aortic Valve Disease 40 0.044
968
MCR014 Microcystic Adenoma 38 0.044
969
ENC014 Enchondroma 38 0.044
970
SVR029 Severe Combined Immunodeficiency, T Cell-Negative, B-Cell/natural Killer-Cell Positive 35 0.044
971
PLY010 Polyclonal Hypergammaglobulinemia 34 0.044
972
XLN003 X-Linked Sideroblastic Anemia with Ataxia 34 0.044
973
c ATM029 Autoimmune Lymphoproliferative Syndrome, Type Ib 33 0.044
974
P SYS007 Systemic Capillary Leak Syndrome 32 0.044
975
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 32 0.044
976
GRD005 Geroderma Osteodysplasticum 31 0.044
977
P MGL002 Megalencephalic Leukoencephalopathy with Subcortical Cysts 31 0.044
978
BRD025 Birdshot Chorioretinopathy 30 0.044
979
IDP021 Idiopathic Myopathy 29 0.044
980
ECT004 Ecthyma 29 0.044
981
P IRD006 Iridogoniodysgenesis, Dominant Type 28 0.044
982
PTL001 Patulous Eustachian Tube 28 0.044
983
END048 Endotoxin Hyporesponsiveness 28 0.044
984
DNG004 Dengue Fever, Protection Against 26 0.044
985
BRR005 Barraquer-Simons Syndrome 26 0.044
986
c GLM039 Glomerulosclerosis, Focal Segmental, 6 24 0.044
987
P MYP018 Myopia 6 23 0.044
988
RHB020 Rhabdomyosarcoma, Somatic 23 0.044
989
P EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 23 0.044
990
LNR006 Linear Iga Disease 22 0.044
991
TCL012 T-Cell/histiocyte Rich Large B Cell Lymphoma 19 0.044
992
c LKN016 Leukoencephalopathy with Mild Cerebellar Ataxia and White Matter Edema 11 0.044
993
CRH001 Crohn's Disease 78 0.042
994
P WSK001 Wiskott-Aldrich Syndrome 76 0.042
995
P FML018 Familial Mediterranean Fever 73 0.042
996
MNK001 Menkes Disease 71 0.042
997
P OST018 Osteosarcoma 70 0.042
998
CLD001 Cleidocranial Dysplasia 68 0.042
999
ADN018 Adenoma 67 0.042
1000
ANT006 Antiphospholipid Syndrome 64 0.042
1001
P TMP003 Temporal Arteritis 64 0.042
1002
P ANR007 Anorexia Nervosa 64 0.042
1003
c PRM002 Primary Hyperoxaluria 63 0.042
1004
PLY017 Polyarteritis Nodosa 62 0.042
1005
PMS001 Poems Syndrome 61 0.042
1006
BRN002 Bronchiolitis 60 0.042
1007
ALP001 Alopecia Universalis 59 0.042
1008
HYP014 Hyperuricemia 58 0.042
1009
P BRN012 Bronchiolitis Obliterans 58 0.042
1010
GLL022 Guillain-Barre Syndrome 54 0.042
1011
PYR013 Pyruvate Kinase Deficiency 54 0.042
1012
INT075 Intracranial Hypertension 53 0.042
1013
ORL005 Oral Candidiasis 53 0.042
1014
CLD007 Cold Agglutinin Disease 52 0.042
1015
MRK001 Merkel Cell Carcinoma 52 0.042
1016
PRP007 Priapism 52 0.042
1017
PRS047 Prostatitis 50 0.042
1018
HYP005 Hypokalemia 50 0.042
1019
PRM027 Primitive Neuroectodermal Tumor 50 0.042
1020
ACT100 Acute Febrile Neutrophilic Dermatosis 49 0.042
1021
MLT113 Multicentric Castleman Disease 48 0.042
1022
IMM001 Immune-Complex Glomerulonephritis 47 0.042
1023
c BLT006 Bilateral Breast Cancer 47 0.042
1024
SCB001 Scabies 45 0.042
1025
22Q001 22q11.2 Duplication 42 0.042
1026
c PRM051 Primary Pigmented Nodular Adrenocortical Disease 42 0.042
1027
FST010 Fasting Hypoglycemia 40 0.042
1028
c LPR012 Leopard Syndrome 1 39 0.042
1029
AGG002 Aggressive Systemic Mastocytosis 39 0.042
1030
BLD101 Bladder Cancer Susceptibility 38 0.042
1031
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.042
1032
MNN034 Mannose-Binding Lectin Deficiency 37 0.042
1033
VRL011 Viral Infectious Disease 35 0.042
1034
P 2Q3002 2q37 Microdeletion Syndrome 34 0.042
1035
MYL013 Myeloperoxidase Deficiency 34 0.042
1036
PYR016 Pyridoxine Deficiency 33 0.042
1037
MN1001 Mn1 33 0.042
1038
CMP001 Composite Lymphoma 31 0.042
1039
CLL005 Cellular Leiomyoma 30 0.042
1040
P WLM008 Wilms Tumor, Type 1 29 0.042
1041
NRW001 Norwegian Scabies 28 0.042
1042
c 2P2001 2p21 Microdeletion Syndrome 25 0.042
1043
PTS004 Potassium Aggravated Myotonia 23 0.042
1044
TRN028 Transient Acantholytic Dermatosis 23 0.042
1045
BLD025 Bladder Sarcoma 20 0.042
1046
CD4007 Cd4+/cd56+ Hematodermic Neoplasm 16 0.042
1047
SVR037 Severe Combined Immune Deficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative, Jak3-Related 15 0.042
1048
c CLD010 Cold-Induced Sweating Syndrome 1 12 0.042
1049
THY028 Thyroid Cancer 73 0.040
1050
KPS001 Kaposi's Sarcoma 73 0.040
1051
P AST007 Astrocytoma 70 0.040
1052
KWS002 Kawasaki Disease 69 0.040
1053
VSC007 Vascular Disease 69 0.040
1054
P CRN008 Carney Complex 68 0.040
1055
ESP021 Esophageal Cancer 68 0.040
1056
PRT036 Peritonitis 67 0.040
1057
INF030 Infectious Mononucleosis 65 0.040
1058
TKY001 Takayasu's Arteritis 65 0.040
1059
PRC002 Paracoccidioidomycosis 64 0.040
1060
P FCL005 Focal Segmental Glomerulosclerosis 64 0.040
1061
P DDN001 Duodenal Ulcer 63 0.040
1062
MSL001 Measles 62 0.040
1063
c ACT075 Acute Myocardial Infarction 59 0.040
1064
MLT001 Multiple Chemical Sensitivity 58 0.040
1065
INT051 Intussusception 57 0.040
1066
c ENC004 Encephalitis 56 0.040
1067
P MMP001 Mumps 56 0.040
1068
c THR003 Thoracic Aortic Aneurysm 54 0.040
1069
HYP003 Hypermethioninemia 52 0.040
1070
CHR074 Choriocarcinoma 52 0.040
1071
PRM126 Primary Peritoneal Carcinoma 51 0.040
1072
FNC040 Fanconi Bickel Syndrome 51 0.040
1073
CHC001 Chickenpox 51 0.040
1074
TCL003 T Cell Deficiency 51 0.040
1075
c ATM019 Autoimmune Polyendocrine Syndrome 51 0.040
1076
SMT019 Somatostatin Analog 51 0.040
1077
c CNT016 Central Retinal Vein Occlusion 50 0.040
1078
GST050 Gastrointestinal System Disease 50 0.040
1079
ACT008 Actinic Keratosis 49 0.040
1080
RHB017 Rhabdoid Tumor 49 0.040
1081
PLR008 Pleurisy 46 0.040
1082
LKM006 Leukomalacia 45 0.040
1083
ONC003 Oncogenic Osteomalacia 45 0.040
1084
TXC002 Toxic Encephalopathy 45 0.040
1085
INF034 Infective Endocarditis 44 0.040
1086
c ADN012 Adenocarcinoma in Situ 43 0.040
1087
P LSS005 Lissencephaly 1 42 0.040
1088
DYS006 Dysembryoplastic Neuroepithelial Tumor 40 0.040
1089
GLS007 Glossitis 40 0.040
1090
STC004 Stachybotrys Chartarum 39 0.040
1091
ENT007 Enteropathica 38 0.040
1092
c CNG029 Congenital Mesoblastic Nephroma 38 0.040
1093
ANG037 Angiomatosis 37 0.040
1094
PRL008 Paralytic Ileus 37 0.040
1095
GRN037 Granulomatosis with Polyangiitis 36 0.040
1096
PST062 Pustulosis Palmaris Et Plantaris 36 0.040
1097
FLL036 Follicular Dendritic Cell Tumor 34 0.040
1098
IDP041 Idiopathic Recurrent Pericarditis 33 0.040
1099
BRC011 Brachial Plexus Neuropathy 31 0.040
1100
FNC027 Fanconi Anemia, Complementation Group a 29 0.040
1101
LNG004 Langerhans Cell Sarcoma 28 0.040
1102
PHS016 Phosphorylase Kinase Deficiency of Liver and Muscle, Autosomal Recessive 26 0.040
1103
RHB022 Rhabdoid Tumors, Somatic 25 0.040
1104
CHR158 Charles Bonnet Syndrome 25 0.040
1105
RDT006 Radiation Induced Meningioma 25 0.040
1106
P CHR259 Chromosome 6q25 Microdeletion Syndrome 22 0.040
1107
NNF003 Non-Familial Renal Cell Carcinoma 19 0.040
1108
CLN005 Colon Lymphoma 19 0.040
1109
10Q001 10q22.3q23.3 Microdeletion Syndrome 19 0.040
1110
c VCT004 Vacterl Association with Hydrocephalus 13 0.040
1111
OTP003 Oto-Palatal-Digital Syndrome 13 0.040
1112
c CHR257 Chromosome 6q Deletion 12 0.040
1113
NNH003 Non-Hodgkin Lymphoma, Childhood 12 0.040
1114
c 2Q2002 2q23.1 Microduplication Syndrome 10 0.040
1115
P LPR003 Leprosy 67 0.038
1116
P BRD002 Bardet-Biedl Syndrome 67 0.038
1117
HYP056 Hypoglycemia 66 0.038
1118
CNG368 Congenital Adrenal Hyperplasia 64 0.038
1119
c HPT016 Hepatitis B 62 0.038
1120
SML001 Small Cell Carcinoma 62 0.038
1121
P DGR001 Digeorge Syndrome 60 0.038
1122
MXD005 Mixed Connective Tissue Disease 60 0.038
1123
ANG020 Angiosarcoma 58 0.038
1124
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 57 0.038
1125
LST001 Listeriosis 56 0.038
1126
MYX005 Myxoid Liposarcoma 56 0.038
1127
ACT049 Acute Disseminated Encephalomyelitis 56 0.038
1128
ERY003 Erythema Multiforme 56 0.038
1129
P FBR017 Fibrosarcoma 56 0.038
1130
WLL006 Wells Syndrome 55 0.038
1131
FDL002 Food Allergy 55 0.038
1132
P CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 54 0.038
1133
ESN015 Eosinophilic Fasciitis 54 0.038
1134
BCT002 Bacterial Vaginosis 53 0.038
1135
P RTN022 Retinal Vein Occlusion 53 0.038
1136
c HPT007 Hepatitis E 52 0.038
1137
PRN011 Pernicious Anemia 52 0.038
1138
GNG002 Ganglioneuroma 51 0.038
1139
P EXP004 Exophthalmos 51 0.038
1140
PLC007 Placental Abruption 51 0.038
1141
CWP001 Cowpox 49 0.038
1142
PPL020 Papillary Thyroid Carcinoma 49 0.038
1143
TNG003 Tongue Cancer 49 0.038
1144
P END047 Endophthalmitis 48 0.038
1145
LCH009 Lichen Sclerosus 47 0.038
1146
IMP002 Imperforate Anus 47 0.038
1147
c ACT076 Acute Myocarditis 47 0.038
1148
RTN001 Retinal Vasculitis 44 0.038
1149
LYM024 Lymphatic System Disease 44 0.038
1150
MLK003 Melkersson-Rosenthal Syndrome 43 0.038
1151
c SBC035 Subacute Cutaneous Lupus Erythematosus 42 0.038
1152
c MSB002 Mesoblastic Nephroma 42 0.038
1153
FML027 Female Breast Carcinoma 42 0.038
1154
LYM012 Lymphoplasmacytic Lymphoma 40 0.038
1155
CDQ001 Cauda Equina Syndrome 39 0.038
1156
GBL002 Goblet Cell Carcinoid 38 0.038
1157
ORB011 Orbit Rhabdomyosarcoma 38 0.038
1158
CVR010 Cavernous Malformation 37 0.038
1159
c BRC013 Brachydactyly Type E 36 0.038
1160
ATY012 Atypical Mycobacteriosis, Familial 35 0.038
1161
BNG041 Benign Metastasizing Leiomyoma 35 0.038
1162
SRC001 Sarcomatoid Mesothelioma 34 0.038
1163
FLM003 Fulminant Viral Hepatitis 30 0.038
1164
AML004 Ameloblastic Carcinoma 29 0.038
1165
P PLM064 Pulmonary Sequestration 25 0.038
1166
MYL002 Myelophthisic Anemia 24 0.038
1167
c NNN010 Noonan Syndrome 3 22 0.038
1168
FML233 Familial Papillary Thyroid Carcinoma with Renal Papillary Neoplasia 20 0.038
1169
CNJ009 Conjunctival Cancer 18 0.038
1170
GRN011 Granulomatous Gastritis 17 0.038
1171
P OST002 Osteoporosis 73 0.036
1172
CRZ001 Crouzon Syndrome 67 0.036
1173
GST023 Gastric Ulcer 67 0.036
1174
P LSH001 Leishmaniasis 65 0.036
1175
P THR015 Thrombophilia 65 0.036
1176
CMM004 Common Variable Immunodeficiency 64 0.036
1177
c HMP007 Hemophilia 64 0.036
1178
SPN038 Spina Bifida 63 0.036
1179
AMN001 Amenorrhea 63 0.036
1180
THR016 Thrombophlebitis 61 0.036
1181
P CHR071 Charcot-Marie-Tooth Disease 61 0.036
1182
PPL002 Papillary Carcinoma 60 0.036
1183
PPL022 Papilloma 60 0.036
1184
LPR001 Lepromatous Leprosy 59 0.036
1185
ALP008 Alopecia 59 0.036
1186
GNT003 Genital Herpes 59 0.036
1187
PLM014 Pleomorphic Adenoma 59 0.036
1188
P RHN004 Rhinitis 59 0.036
1189
P CST002 Castleman's Disease 58 0.036
1190
SHW002 Shwachman-Diamond Syndrome 58 0.036
1191
MCR088 Microscopic Polyangiitis 58 0.036
1192
CHR001 Churg-Strauss Syndrome 56 0.036
1193
SCR008 Scrub Typhus 55 0.036
1194
ANT011 Antisocial Personality Disorder 55 0.036
1195
P PRT008 Proteus Syndrome 55 0.036
1196
HYP458 Hyper Ige Syndrome 54 0.036
1197
URM002 Uremia 54 0.036
1198
c BLN003 Blindness 54 0.036
1199
CRV035 Cervical Cancer 54 0.036
1200
P LRY019 Laryngitis 53 0.036
1201
P MND007 Mandibuloacral Dysplasia 53 0.036
1202
P MLG077 Malignant Peripheral Nerve Sheath Tumor 53 0.036
1203
BNF002 Bone Fracture 53 0.036
1204
SPN020 Spondylosis 53 0.036
1205
NRH001 Neurohypophyseal Diabetes Insipidus 52 0.036
1206
DNG003 Dengue Disease 52 0.036
1207
ALX001 Alexia 51 0.036
1208
PRM042 Primary Effusion Lymphoma 51