Search results for "leukemia"

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

2204 hits were found for 'leukemia'

# Family MCID Name MIFTS Score
1
P MYL006 Myeloid Leukemia 64 7.513
2
P LKM002 Leukemia 66 7.449
3
P CHR090 Chronic Lymphocytic Leukemia 74 5.936
4
c LKM062 Leukemia, Acute Lymphoblastic 58 5.930
5
c LKM061 Leukemia, Acute Myeloid 69 5.188
6
ACT095 Acute Biphenotypic Leukemia 49 5.175
7
c LKM063 Leukemia, Chronic Myeloid 53 5.121
8
LKM065 Leukemia, Acute Promyelocytic 47 4.865
9
c ACT073 Acute Leukemia 48 4.405
10
c LKM064 Leukemia, Juvenile Myelomonocytic 45 4.317
11
c ACT009 Acute Monocytic Leukemia 50 4.207
12
MGK001 Megakaryocytic Leukemia 40 4.060
13
P LYM026 Lymphoblastic Leukemia 55 4.041
14
c ADL017 Adult T-Cell Leukemia 40 3.891
15
c ACT115 Acute Myeloid Leukemia, Adult 27 3.801
16
NTR003 Natural Killer Cell Leukemia 49 3.661
17
c ACT020 Acute T Cell Leukemia 28 3.582
18
HCL001 Hcl-V 43 3.543
19
P TCL004 T-Cell Leukemia 43 3.418
20
c CHR285 Chronic Myelomonocytic Leukemia 48 3.304
21
P MNC007 Monocytic Leukemia 49 3.091
22
LRG008 Large Granular Lymphocyte Leukemia 35 3.091
23
ACT098 Acute Erythroid Leukemia 34 3.045
24
BLS007 Blastic Plasmacytoid Dendritic Cell 45 3.005
25
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 15 2.994
26
c SBC004 Subacute Myeloid Leukemia 18 2.948
27
P ACT117 Acute Myelomonocytic Leukemia 54 2.932
28
c ADL052 Adult Acute Lymphocytic Leukemia 46 2.892
29
P PRC048 Precursor B-Cell Acute Lymphoblastic Leukemia 47 2.844
30
c PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 40 2.803
31
FML155 Familial Acute Myeloid Leukemia with Mutated Cebpa 10 2.735
32
PRL017 Prolymphocytic Leukemia 36 2.704
33
PLS016 Plasma Cell Leukemia 42 2.702
34
TCL002 T-Cell Large Granular Lymphocyte Leukemia 36 2.671
35
CHL061 Childhood Leukemia 31 2.592
36
c LKM005 Leukemia, T-Cell, Chronic 15 2.537
37
SQM013 Squamous Cell Carcinoma, Head and Neck 64 2.503
38
ACT103 Acute Lymphoblastic Leukemia, Childhood 13 2.499
39
CHR286 Chronic Neutrophilic Leukemia 42 2.493
40
CNT018 Central Nervous System Leukemia 35 2.406
41
c SYS004 Systemic Mastocytosis 60 2.385
42
ACT113 Acute Myeloblastic Leukemia with Maturation 31 2.279
43
ACT114 Acute Myeloblastic Leukemia Without Maturation 25 2.262
44
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 17 2.247
45
SBL003 Subleukemic Leukemia 10 2.247
46
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 24 2.225
47
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 9 2.214
48
LYM067 Lymphoid Leukemia 37 2.181
49
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 25 2.145
50
MST002 Mast-Cell Leukemia 30 2.120
51
c CHR418 Chronic Leukemia 30 2.093
52
TST003 Testicular Leukemia 15 2.019
53
P LFR001 Li-Fraumeni Syndrome 81 1.999
54
c CHR064 Chronic Monocytic Leukemia 15 1.961
55
NLL001 Null-Cell Leukemia 8 1.939
56
NNN022 Noonan Syndrome-Like Disorder with or Without Juvenile Myelomonocytic Leukemia 22 1.934
57
c LKM004 Leukemia, B-Cell, Chronic 16 1.934
58
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 6 1.916
59
CRB138 Core Binding Factor Acute Myeloid Leukemia 37 1.770
60
ACT118 Acute Non Lymphoblastic Leukemia 22 1.767
61
ACT177 Acute Basophilic Leukemia 33 1.724
62
ALK003 Aleukemic Leukemia Cutis 15 1.718
63
c HMN021 Human T-Cell Leukemia Virus Type 1 37 1.710
64
RFR002 Refractory Hairy Cell Leukemia 11 1.647
65
NNT007 Neonatal Leukemia 18 1.644
66
ACT097 Acute Erythroblastic Leukemia 7 1.637
67
P 8P1002 8p11 Myeloproliferative Syndrome 32 1.634
68
CLL014 Cll/sll 25 1.630
69
ACT178 Acute Myeloid Leukemia with Multilineage Dysplasia 15 1.630
70
c SBC006 Subacute Leukemia 10 1.618
71
c PRC018 Precursor T-Lymphoblastic Lymphoma/leukemia 11 1.605
72
ALK002 Aleukemic Monocytic Leukemia Cutis 7 1.600
73
MYL048 Myelodysplasia and Leukemia Syndrome with Monosomy 7 20 1.595
74
c SBC015 Subacute Monocytic Leukemia 10 1.595
75
PLS003 Plasmacytic Leukemia 10 1.589
76
SPL013 Splenic Manifestation of Leukemia 5 1.583
77
PDT026 Pediatric T-Cell Leukemia 3 1.583
78
c INH015 Inherited Acute Myeloid Leukemia 13 1.577
79
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 9 1.570
80
HRY001 Hairy Cell Leukemia of Spleen 7 1.570
81
NNN023 Noonan Syndrome-Like Disorder with Juvenile Myelomonocytic Leukemia 6 1.570
82
P FML096 Familial Acute Myelocytic Leukemia 5 1.570
83
PRG005 Pregerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 5 1.570
84
PST004 Postgerminal Center Chronic Lymphocytic Leukemia/small Lymphocytic Lymphoma 5 1.570
85
CHL029 Childhood Precursor T-Lymphoblastic Lymphoma/leukemia 4 1.570
86
SPL002 Splenic Manifestation of Prolymphocytic Leukemia 2 1.570
87
SPL010 Splenic Manifestation of Hairy Cell Leukemia 2 1.570
88
LYM040 Lymphoblastic Lymphoma 49 1.383
89
c HMN022 Human T-Cell Leukemia Virus Type 2 36 1.276
90
P HYP098 Hypereosinophilic Syndrome 55 1.265
91
c FML114 Familial Chronic Lymphocytic Leukemia 32 1.255
92
PHL007 Philadelphia-Negative Chronic Myeloid Leukemia 23 1.209
93
c ACT208 'acute Myeloid Leukemia with T(8;21)(q22;q22) Translocation' 27 1.188
94
ACT207 'acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)' 27 1.172
95
FML045 Familial Mosaic Monosomy 7 Syndrome 13 1.163
96
ALK014 Aleukemic Mast Cell Leukemia 11 1.163
97
c ACT203 'acute Myeloid Leukemia with T(9;11)(p22;q23)' 17 1.158
98
DFN226 Deafness - Lymphedema - Leukemia 20 1.153
99
P ACT190 Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation 17 1.153
100
c FML095 Familial Acute Lymphocytic Leukemia 8 1.153
101
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 18 1.147
102
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 10 1.147
103
P PPL026 Papular Mucinosis 23 1.141
104
c ACT205 'acute Myeloid Leukemia with T(6;9)(p23;q34)' 11 1.141
105
BLN016 Bilineal Acute Leukemia 8 1.141
106
c HMN023 Human T-Cell Leukemia Virus Type 3 6 1.141
107
FML146 Familial Platelet Disorder with Propensity to Acute Myelogenous Leukemia 6 1.141
108
c MYL018 Myelocytic Leukemia-Like Syndrome, Familial, Chronic 4 1.141
109
ACT116 Acute Myeloid Leukemia, Childhood 4 1.141
110
P ACT106 Acute Myeloblastic Leukemia Type 1 2 1.135
111
c ACT107 Acute Myeloblastic Leukemia Type 2 2 1.135
112
c ACT111 Acute Myeloblastic Leukemia Type 6 2 1.135
113
c ACT112 Acute Myeloblastic Leukemia Type 7 2 1.135
114
NSY001 N Syndrome 30 1.128
115
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 13 1.128
116
MYL041 Myeloid Neoplasm Associated with Fgfr1 Rearrangement 12 1.128
117
MGK006 'megakaryoblastic Acute Myeloid Leukemia with T(1;22)(p13;q13)' 9 1.128
118
MNM003 Minimally Differentiated Acute Myeloblastic Leukemia 7 1.128
119
c FML115 Familial Chronic Myelocytic Leukemia 4 1.128
120
ACT102 Acute Lymphoblastic Leukemia Congenital Sporadic Aniridia 2 1.128
121
c ACT109 Acute Myeloblastic Leukemia Type 4 1 1.128
122
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 10 1.120
123
c LKM060 Leukemia, Acute Lymphoblastic 3 8 1.120
124
c NPM001 Npm1-Related Acute Myeloid Leukemia 8 1.120
125
ACT166 Acute Myeloid Leukemia with Cebpa Somatic Mutations 7 1.120
126
ACT204 'acute Myeloid Leukemia with Inv3(p21;q26.2) or T(3;3)(p21;q26.2)' 7 1.120
127
ACT185 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Topoisomerase Type 2 Inhibitor 5 1.120
128
ACT199 Acute Myeloid Leukemia with Npm1 Somatic Mutations 5 1.120
129
CLS019 Classic Mast Cell Leukemia 5 1.120
130
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 5 1.120
131
BND002 B- and T-Cell Mixed Leukemia 4 1.120
132
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 4 1.120
133
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 4 1.120
134
ACT157 Acute Myeloid Leukemia, Susceptibility, Gata2-Related 4 1.120
135
PRC009 Precursor T-Lymphoblastic Lymphoma/leukemia Refractory 3 1.120
136
WTL001 Wt Limb Blood Syndrome 20 1.097
137
MYL009 Myelodysplastic Syndrome 67 0.311
138
HMT018 Hematopoietic Stem Cell Transplantation 36 0.216
139
P MYL007 Myeloma 53 0.193
140
SRC014 Sarcoma 61 0.185
141
END072 Endotheliitis 44 0.163
142
c MLT019 Multiple Myeloma 75 0.163
143
DWN001 Down Syndrome 51 0.150
144
P MYL005 Myelofibrosis 68 0.144
145
P WLM002 Wilms Tumor 70 0.143
146
P NTR004 Neutropenia 56 0.140
147
P HPT021 Hepatitis 55 0.133
148
P MST009 Mastocytosis 61 0.130
149
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.129
150
LYM019 Lymphosarcoma 50 0.128
151
P BCL006 B-Cell Lymphomas 47 0.128
152
P HML002 Hemolytic Anemia 56 0.127
153
MYL003 Myeloid Sarcoma 48 0.127
154
P BRS047 Breast Cancer 90 0.125
155
P ESN007 Eosinophilia 54 0.124
156
THR013 Thoracic Outlet Syndrome 45 0.124
157
HDG012 Hodgkin Lymphoma 79 0.123
158
P HYP004 Hypercalcemia 57 0.119
159
RFR010 Refractory Anemia 42 0.119
160
P TRC086 Trichohepatoenteric Syndrome 1 39 0.117
161
c ATM010 Autoimmune Hemolytic Anemia 57 0.115
162
P HST010 Histiocytosis 55 0.111
163
P ATX030 Ataxia-Telangiectasia 76 0.110
164
P RHM011 Rheumatoid Arthritis 94 0.105
165
P ART022 Arthritis 65 0.105
166
c BNG076 Benign Exophthalmos Syndrome 19 0.105
167
P ESS003 Essential Thrombocythemia 66 0.104
168
BRK010 Burkitt Lymphoma 63 0.104
169
P THR014 Thrombocytopenia 56 0.103
170
ACN002 Acanthosis Nigricans 55 0.103
171
PRS047 Prostatitis 51 0.103
172
PRR002 Pure Red-Cell Aplasia 46 0.103
173
P APL001 Aplastic Anemia 76 0.102
174
P ATX010 Ataxia Neuropathy Spectrum 29 0.102
175
RCH001 Richter's Syndrome 29 0.101
176
PLY001 Polycythemia Vera 75 0.099
177
P PLY018 Polycythemia 58 0.099
178
P PNM007 Pneumonia 64 0.096
179
ASP006 Aspergillosis 63 0.096
180
P MNN013 Meningitis 58 0.096
181
LKS001 Leukostasis 42 0.096
182
SPS019 Spastic Paraparesis 35 0.096
183
SPS057 Spasticity 32 0.096
184
P NRF002 Neurofibromatosis 69 0.095
185
SVR004 Severe Combined Immunodeficiency 68 0.095
186
DSS009 Disseminated Intravascular Coagulation 52 0.095
187
VSC011 Vasculitis 57 0.094
188
BNM005 Bone Marrow Necrosis 33 0.094
189
P ANG001 Angelman Syndrome 66 0.093
190
c SPN225 Spondyloarthropathy 1 48 0.093
191
c ART101 Aortic Valve Disease 2 32 0.093
192
MNT001 Mantle Cell Lymphoma 55 0.092
193
GLC037 Glucocorticoid Resistance 48 0.092
194
TRP002 Tropical Spastic Paraparesis 46 0.092
195
P THY032 Thyroiditis 56 0.090
196
CRB009 Cerebritis 33 0.090
197
HPT023 Hepatocellular Carcinoma 95 0.089
198
AND015 Androgen Insensitivity 69 0.089
199
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.089
200
TTR011 Tetraploidy 52 0.089
201
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.089
202
THR004 Thrombocytosis 50 0.089
203
MCR004 Macroglobulinemia 48 0.089
204
LKM001 Leukemoid Reaction 41 0.086
205
MLN008 Melanoma 55 0.085
206
c SVR003 Severe Congenital Neutropenia 44 0.085
207
RTN023 Retinitis 44 0.085
208
P NRP001 Neuropathy 52 0.084
209
HV1006 Hiv-1 83 0.082
210
P RTN024 Retinoblastoma 75 0.082
211
c MLG054 Malignant Histiocytosis 55 0.082
212
DPH001 Diphtheria 47 0.082
213
P PNC001 Pancytopenia 41 0.082
214
MDS022 Mediastinitis 39 0.082
215
P ATX004 Ataxia 50 0.081
216
P LNG032 Lung Cancer 94 0.080
217
P PRS040 Prostate Cancer 84 0.078
218
P DBT005 Diabetes Insipidus 53 0.078
219
BCT015 Bacteremia 45 0.078
220
P AND016 Andersen Syndrome 54 0.077
221
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 51 0.077
222
ART001 Arterial Tortuosity Syndrome 48 0.077
223
GRN017 Granulocytopenia 42 0.077
224
PRP030 Purpura 54 0.075
225
GNG013 Gingivitis 52 0.075
226
HYP266 Hypoxia 49 0.075
227
P ADN016 Adenocarcinoma 49 0.075
228
P ACT135 Acute Graft Versus Host Disease 44 0.075
229
P NRB001 Neuroblastoma 68 0.074
230
P PNC044 Pancreatitis 59 0.074
231
P GLM007 Glomerulonephritis 59 0.074
232
CHR066 Chronic Fatigue Syndrome 55 0.074
233
HMT002 Hematologic Cancer 52 0.074
234
c CHR417 Chronic Graft Versus Host Disease 37 0.074
235
TFT003 Tufting Enteropathy 26 0.074
236
DFF005 Diffuse Large B-Cell Lymphoma 50 0.072
237
HST016 Histiocytic Sarcoma 44 0.072
238
HMG002 Hemoglobinuria 43 0.072
239
SPL018 Splenomegaly 40 0.072
240
P INF038 Influenza 67 0.071
241
MYC002 Mycobacterium Avium Complex Disease 51 0.071
242
ZYG002 Zygomycosis 39 0.071
243
P HRP006 Herpes Simplex 63 0.069
244
LNG024 Langerhans-Cell Histiocytosis 51 0.069
245
P PLM006 Pulmonary Alveolar Proteinosis 47 0.069
246
INV001 Invasive Aspergillosis 44 0.069
247
OST003 Osteonecrosis 49 0.067
248
NRN002 Neuronitis 36 0.067
249
UND005 Undifferentiated Pleomorphic Sarcoma 28 0.067
250
AND005 Androgen Insensitivity Syndrome, Mild 17 0.067
251
P OBS005 Obesity 94 0.066
252
TBR010 Tuberculosis 73 0.066
253
c NRF018 Neurofibromatosis, Type 1 65 0.066
254
c HPT016 Hepatitis B 60 0.066
255
c HPT001 Hepatitis C 57 0.066
256
SMT008 Smith-Magenis Syndrome 56 0.066
257
P CND004 Candidiasis 54 0.066
258
P ANP001 Anaplastic Large Cell Lymphoma 53 0.066
259
P PLY019 Polyneuropathy 52 0.066
260
P BLN003 Blindness 47 0.066
261
PRG009 Progressive Multifocal Leukoencephalopathy 45 0.066
262
BNM001 Bone Marrow Cancer 43 0.066
263
c CNT035 Central Nervous System Disease 42 0.066
264
HYP084 Hypopyon 21 0.066
265
P AMY004 Amyloidosis 63 0.064
266
MYC006 Mycosis Fungoides 62 0.064
267
P NJM001 Nijmegen Breakage Syndrome 61 0.064
268
URT039 Urticaria 55 0.064
269
CTN014 Cutaneous Mastocytosis 53 0.064
270
P RFR008 Refractory Anemia with Excess Blasts 29 0.064
271
GST019 Gastrointestinal Stromal Tumor 74 0.062
272
ABT001 Abetalipoproteinemia 63 0.062
273
DRM006 Dermatitis 58 0.062
274
P PRP029 Porphyria 57 0.062
275
CLT003 Colitis 54 0.062
276
HYP063 Hypersplenism 50 0.062
277
c CHR092 Chronic Myeloproliferative Disease 43 0.062
278
FLL019 Follicular Mucinosis 33 0.062
279
ADS002 Adie Syndrome 30 0.062
280
HNM002 Hinman Syndrome 26 0.062
281
FSR001 Fusariosis 23 0.062
282
PMP001 Pemphigus 51 0.060
283
FLL037 Follicular Lymphoma 50 0.060
284
HRP004 Herpes Zoster 49 0.060
285
c JVN003 Juvenile Xanthogranuloma 46 0.060
286
PLS025 Plasmablastic Lymphoma 46 0.060
287
PRP023 Peripheral Neuropathy 44 0.060
288
LKP004 Leukopenia 38 0.060
289
P SDR003 Sideroblastic Anemia 38 0.060
290
HYP025 Hyperphosphatemia 36 0.060
291
TTR021 Tetrasomy 21 24 0.060
292
PRP003 Porphyria Cutanea Tarda 69 0.058
293
P RSP003 Respiratory Failure 62 0.058
294
P GLB002 Glioblastoma 59 0.058
295
P UVT001 Uveitis 57 0.058
296
c HPT073 Hepatitis C Virus 51 0.058
297
SCB001 Scabies 50 0.058
298
RHB003 Rhabdomyosarcoma 49 0.058
299
PRC012 Pericardial Effusion 49 0.058
300
c PND001 Pain Disorder 46 0.058
301
URT008 Urticaria Pigmentosa 38 0.058
302
EMN001 Emanuel Syndrome 36 0.058
303
IPX001 Ipex Syndrome 32 0.058
304
c SYS001 Systemic Lupus Erythematosus 91 0.056
305
c FNC027 Fanconi Anemia, Complementation Group a 68 0.056
306
P RBN001 Rubinstein-Taybi Syndrome 67 0.056
307
P LPS004 Lupus Erythematosus 67 0.056
308
GLN010 Glanzmann Thrombasthenia 63 0.056
309
P AST007 Astrocytoma 63 0.056
310
P SNS014 Sinusitis 56 0.056
311
MGL001 Megaloblastic Anemia 56 0.056
312
PRT011 Protein C Deficiency 54 0.056
313
HYP066 Hyperglycemia 52 0.056
314
PLS011 Plasmacytoma 49 0.056
315
P CRV039 Cervicitis 49 0.056
316
P IDP064 Idiopathic Neutropenia 46 0.056
317
AGG002 Aggressive Systemic Mastocytosis 45 0.056
318
P CTN015 Cutaneous T Cell Lymphoma 45 0.056
319
P LCT001 Lactic Acidosis 42 0.056
320
DND018 Dendritic Cell Tumor 41 0.056
321
CYT008 Cytomegalovirus Infection 39 0.056
322
P RNL014 Renal Cell Carcinoma 83 0.054
323
P ENC004 Encephalitis 56 0.054
324
FLT001 Felty's Syndrome 55 0.054
325
DFC004 Deficiency Anemia 54 0.054
326
P ACR001 Aicardi-Goutieres Syndrome 54 0.054
327
PRP007 Priapism 51 0.054
328
PSD002 Pseudotumor Cerebri 47 0.054
329
KLN001 Klinefelter's Syndrome 47 0.054
330
THY009 Thyroid Lymphoma 46 0.054
331
EWN002 Ewing's Family of Tumors 46 0.054
332
INT221 Intravascular Large B-Cell Lymphoma 46 0.054
333
PRT039 Proteinuria 43 0.054
334
CLN015 Colon Adenocarcinoma 43 0.054
335
PYM001 Pyomyositis 42 0.054
336
RTC005 Reticulosarcoma 37 0.054
337
c JVN024 Juvenile Hereditary Hemochromatosis 25 0.054
338
c AMY091 Amyotrophic Lateral Sclerosis 1 82 0.052
339
P MYC007 Myocardial Infarction 81 0.052
340
P LPR002 Leopard Syndrome 67 0.052
341
P NNN008 Noonan Syndrome 1 66 0.052
342
GLL008 Gilles De La Tourette Syndrome 64 0.052
343
P FRD001 Friedreich Ataxia 61 0.052
344
P NPH012 Nephrotic Syndrome 60 0.052
345
BRN028 Brain Cancer 56 0.052
346
c ACT027 Acute Pancreatitis 55 0.052
347
P OLG002 Oligodendroglioma 55 0.052
348
P FTL001 Fetal Alcohol Syndrome 54 0.052
349
HPT022 Hepatoblastoma 53 0.052
350
ADN001 Adenosine Deaminase Deficiency 52 0.052
351
P FML161 Familial Mediterranean Fever, Ar 51 0.052
352
CYT005 Cytomegalovirus Retinitis 48 0.052
353
MRK001 Merkel Cell Carcinoma 48 0.052
354
P INF032 Infertility 46 0.052
355
PRM163 Primary Mediastinal Large B-Cell Lymphoma 46 0.052
356
MST017 Mast Cell Disease 46 0.052
357
GRN007 Granuloma Annulare 44 0.052
358
SFT003 Soft Tissue Sarcoma 44 0.052
359
PRN049 Paraneoplastic Pemphigus 44 0.052
360
P NRV007 Nervous System Disease 42 0.052
361
PRP036 Peripheral T-Cell Lymphoma 42 0.052
362
HYP017 Hypophosphatemia 42 0.052
363
ANP009 Anaplastic Oligodendroglioma 37 0.052
364
BCK006 Back Pain 33 0.052
365
GRF001 Graft-Versus-Host Disease, Protection Against 32 0.052
366
ECT004 Ecthyma 22 0.052
367
CMB003 Combined T Cell and B Cell Immunodeficiency 17 0.052
368
OTP003 Oto-Palatal-Digital Syndrome 14 0.052
369
CRH001 Crohn's Disease 71 0.050
370
P PRM002 Primary Hyperoxaluria 68 0.050
371
DNG003 Dengue Disease 64 0.050
372
P MYS005 Myositis 63 0.050
373
PYR013 Pyruvate Kinase Deficiency 61 0.050
374
P AGM001 Agammaglobulinemia 59 0.050
375
P PTT014 Pitt-Hopkins Syndrome 54 0.050
376
ACT100 Acute Febrile Neutrophilic Dermatosis 48 0.050
377
CRD001 Cardiac Tamponade 46 0.050
378
PRN011 Pernicious Anemia 46 0.050
379
HMR001 Hemorrhagic Thrombocythemia 46 0.050
380
LYM051 Lymphomatoid Granulomatosis 43 0.050
381
MNN014 Mononeuritis 43 0.050
382
P KBK002 Kabuki Syndrome 1 42 0.050
383
c MLG081 Malignant Teratoma 41 0.050
384
ANG046 Angioimmunoblastic T-Cell Lymphoma 34 0.050
385
FCT013 Factor V Leiden Thrombophilia 31 0.050
386
P CLR023 Colorectal Cancer 96 0.048
387
P PLM037 Pulmonary Hypertension 85 0.048
388
P DBT085 Diabetes Mellitus, Insulin-Dependent 83 0.048
389
P DMN001 Diamond-Blackfan Anemia 66 0.048
390
P THL005 Thalassemia 64 0.048
391
P HYP117 Hypertriglyceridemia 61 0.048
392
PLL001 Pallister-Hall Syndrome 61 0.048
393
MSL001 Measles 58 0.048
394
P THY023 Thymoma 57 0.048
395
c ALM001 Al Amyloidosis 56 0.048
396
P LPS002 Liposarcoma 56 0.048
397
P ANT006 Antiphospholipid Syndrome 55 0.048
398
NTR040 Neutropenia, Cyclic 52 0.048
399
PLY041 Polymyositis 51 0.048
400
P MST018 Mesothelioma 51 0.048
401
MLL005 Miller-Dieker Syndrome 50 0.048
402
P TRT010 Teratoma 50 0.048
403
c PST005 Posterior Uveitis 50 0.048
404
CLL003 Cellulitis 50 0.048
405
c NNN013 Noonan Syndrome 6 49 0.048
406
APP008 Appendicitis 48 0.048
407
P END033 Endocarditis 48 0.048
408
P EXN002 Exanthem 47 0.048
409
P CPL003 Capillary Leak Syndrome 45 0.048
410
P MSB002 Mesoblastic Nephroma 42 0.048
411
HYP005 Hypokalemia 42 0.048
412
MMB001 Membranoproliferative Glomerulonephritis 42 0.048
413
c CNG029 Congenital Mesoblastic Nephroma 41 0.048
414
EVN001 Evans' Syndrome 39 0.048
415
PNN001 Panniculitis 38 0.048
416
CYT004 Cytomegalic Inclusion Disease 28 0.048
417
TRS012 Trisomy 22 25 0.048
418
HPT070 Hepatosplenic T-Cell Lymphoma 22 0.048
419
ACT176 Acute Panmyelosis with Myelofibrosis 19 0.048
420
BLM001 Bloom Syndrome 64 0.045
421
STR008 Strongyloidiasis 58 0.045
422
MLT022 Malt Lymphoma 54 0.045
423
P AVS004 Avascular Necrosis of the Femoral Head 54 0.045
424
CLD007 Cold Agglutinin Disease 52 0.045
425
BRN002 Bronchiolitis 52 0.045
426
LYM115 Lymphoma, Non-Hodgkin 51 0.045
427
BRN012 Bronchiolitis Obliterans 50 0.045
428
OST017 Osteomyelitis 50 0.045
429
EXT010 Extramedullary Plasmacytoma 49 0.045
430
CRY004 Cryoglobulinemia 49 0.045
431
TNS005 Tonsillitis 48 0.045
432
PYD001 Pyoderma Gangrenosum 48 0.045
433
DND002 Dendritic Cell Sarcoma 48 0.045
434
c ACT134 Acute Liver Failure 48 0.045
435
PST062 Pustulosis Palmaris Et Plantaris 47 0.045
436
P THR012 Thoracic Cancer 46 0.045
437
PLY020 Polyradiculoneuropathy 46 0.045
438
ACQ007 Acquired Immunodeficiency Syndrome 46 0.045
439
PYD002 Pyoderma 43 0.045
440
P HML001 Hemolytic-Uremic Syndrome 43 0.045
441
LYM027 Lymphopenia 43 0.045
442
LYM045 Lymphocytic Vasculitis 40 0.045
443
GLM011 Glomerulosclerosis 40 0.045
444
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 39 0.045
445
ILS001 Ileus 38 0.045
446
EPG003 Epiglottitis 34 0.045
447
SPR035 Superior Vena Cava Syndrome 34 0.045
448
CMP001 Composite Lymphoma 33 0.045
449
ANG037 Angiomatosis 33 0.045
450
SPL006 Splenic Infarction 32 0.045
451
VRL011 Viral Infectious Disease 31 0.045
452
NRW001 Norwegian Scabies 30 0.045
453
CD4007 Cd4+/cd56+ Hematodermic Neoplasm 21 0.045
454
c HRD009 Hereditary Wilms' Tumor 18 0.045
455
P HMC003 Hemochromatosis 75 0.043
456
P RTT002 Rett Syndrome 73 0.043
457
P MDL005 Medulloblastoma 71 0.043
458
P ATM006 Autoimmune Lymphoproliferative Syndrome 66 0.043
459
SKN016 Skin Disease 64 0.043
460
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 64 0.043
461
ULC004 Ulcerative Colitis 63 0.043
462
c HRD010 Hereditary Spastic Paraplegia 62 0.043
463
c JVN010 Juvenile Rheumatoid Arthritis 59 0.043
464
P HMP007 Hemophilia 59 0.043
465
P RTH001 Rothmund-Thomson Syndrome 58 0.043
466
P LRY019 Laryngitis 56 0.043
467
OST085 Osteosarcoma, Somatic 55 0.043
468
SCK005 Sickle Cell Disease 54 0.043
469
HYP056 Hypoglycemia 53 0.043
470
P MMP001 Mumps 51 0.043
471
WHM001 Whim Syndrome 50 0.043
472
MLR002 Miliary Tuberculosis 50 0.043
473
PLM020 Pleomorphic Xanthoastrocytoma 49 0.043
474
PPL002 Papillary Carcinoma 49 0.043
475
LRY018 Laryngeal Squamous Cell Carcinoma 49 0.043
476
ANR018 Anorchia 48 0.043
477
GST050 Gastrointestinal System Disease 47 0.043
478
NRF008 Neurofibromatosis-Noonan Syndrome 46 0.043
479
GRW007 Growth Hormone Deficiency 46 0.043
480
P DNR001 Duane Retraction Syndrome 44 0.043
481
LYM012 Lymphoplasmacytic Lymphoma 43 0.043
482
PRT026 Parotitis 43 0.043
483
OBS001 Obstructive Jaundice 42 0.043
484
TLN003 Telangiectasis 41 0.043
485
MYX005 Myxoid Liposarcoma 40 0.043
486
LYM021 Lymphadenitis 39 0.043
487
SPR033 Superficial Spreading Melanoma 37 0.043
488
HTL002 Htlv-1 Associated Myelopathy 36 0.043
489
ANR040 Aneurysm 35 0.043
490
TST015 Testicular Disease 35 0.043
491
SPL007 Splenic Abscess 25 0.043
492
IRN002 Iron Metabolism Disease 22 0.043
493
PNM003 Pneumatosis Cystoides Intestinalis 21 0.043
494
c RNG017 Ring Chromosome 21 20 0.043
495
c DNS003 Duane Syndrome Type 1 17 0.043
496
RFR007 Refractory Anemia with Excess Blasts in Transformation 15 0.043
497
P CWD001 Cowden Disease 69 0.040
498
P CRD013 Cardiofaciocutaneous Syndrome 65 0.040
499
HST011 Histoplasmosis 64 0.040
500
THY028 Thyroid Cancer 63 0.040
501
P TMP003 Temporal Arteritis 62 0.040
502
P BCK002 Beckwith-Wiedemann Syndrome 61 0.040
503
P BDD001 Budd-Chiari Syndrome 61 0.040
504
P CHR071 Charcot-Marie-Tooth Disease 60 0.040
505
EWN003 Ewing Sarcoma 59 0.040
506
P FCL005 Focal Segmental Glomerulosclerosis 58 0.040
507
INS024 Insulin-Like Growth Factor I 58 0.040
508
c ACT075 Acute Myocardial Infarction 57 0.040
509
ADN018 Adenoma 55 0.040
510
P ESP024 Esophagitis 54 0.040
511
P ART023 Arthropathy 54 0.040
512
P LMY004 Leiomyosarcoma 53 0.040
513
P MYP004 Myopathy 53 0.040
514
c ACT210 Acute Respiratory Distress Syndrome 52 0.040
515
P FBR017 Fibrosarcoma 52 0.040
516
SRS001 Serous Cystadenocarcinoma 51 0.040
517
P END047 Endophthalmitis 51 0.040
518
MRG003 Marginal Zone B-Cell Lymphoma 51 0.040
519
NRC020 Neuroectodermal Tumor 51 0.040
520
GLL022 Guillain-Barre Syndrome 50 0.040
521
CHN055 Chanarin-Dorfman Syndrome 50 0.040
522
ORL005 Oral Candidiasis 49 0.040
523
P RPD001 Rapidly Progressive Glomerulonephritis 49 0.040
524
FLL008 Folliculitis 49 0.040
525
TLP001 Talipes Equinovarus 48 0.040
526
RTN017 Retinal Detachment 48 0.040
527
DDN006 Duodenitis 48 0.040
528
NCR004 Nocardiosis 47 0.040
529
CRD005 Cardia Cancer 47 0.040
530
ORL011 Oral Cancer 47 0.040
531
NPH051 Nephritis 46 0.040
532
PST046 Post-Transplant Lymphoproliferative Disease 46 0.040
533
c ACQ014 Acquired Hemophilia 45 0.040
534
CHR008 Choroiditis 45 0.040
535
RPP001 Rapp-Hodgkin Syndrome 45 0.040
536
PRC013 Pericarditis 45 0.040
537
c SRC025 Sarcoidosis 1 44 0.040
538
RSC001 Rosacea 43 0.040
539
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 43 0.040
540
RTN001 Retinal Vasculitis 42 0.040
541
BRN013 Bronchiolitis Obliterans Organizing Pneumonia 41 0.040
542
c PRM046 Primary Malignant Lymphoma 41 0.040
543
PRN039 Paraneoplastic Syndromes 40 0.040
544
SPN060 Spondylocarpotarsal Synostosis Syndrome 40 0.040
545
MNC006 Monoclonal Gammopathy of Uncertain Significance 40 0.040
546
LKP003 Leukoplakia 39 0.040
547
P DMY001 Demyelinating Polyneuropathy 39 0.040
548
ECT026 Ectopic Pregnancy 39 0.040
549
UTR043 Uterine Sarcoma 39 0.040
550
THR035 Thrombasthenia 37 0.040
551
GYN001 Gynecomastia 37 0.040
552
TCL003 T Cell Deficiency 37 0.040
553
HDR003 Hidradenitis 37 0.040
554
HPT012 Hepatocellular Fibrolamellar Carcinoma 34 0.040
555
ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 34 0.040
556
CYC007 Cyclic Thrombocytopenia 33 0.040
557
HMR023 Hemorrhagic Cystitis 32 0.040
558
CLC008 Colchicine Resistance 31 0.040
559
PRL008 Paralytic Ileus 30 0.040
560
MYL013 Myeloperoxidase Deficiency 30 0.040
561
INT038 Interdigitating Dendritic Cell Sarcoma 29 0.040
562
MTR008 Mature B-Cell Neoplasm 26 0.040
563
PLY119 Polymicrogyria, Bilateral Perisylvian 26 0.040
564
MYL004 Myelodysplastic Myeloproliferative Cancer 18 0.040
565
c TCL008 T-Cell Lymphoma 1a 10 0.040
566
P ALZ034 Alzheimer Disease 100 0.037
567
GLC006 Galactosemia 75 0.037
568
P PFF001 Pfeiffer Syndrome 74 0.037
569
INC002 Inclusion Body Myositis 71 0.037
570
P GCH001 Gaucher's Disease 70 0.037
571
CMM004 Common Variable Immunodeficiency 67 0.037
572
c HYP595 Hypertension, Essential 66 0.037
573
LKC001 Leukocyte Adhesion Deficiency 65 0.037
574
WLD002 Waldenstrom Macroglobulinemia 56 0.037
575
BLD087 Bladder Cancer, Somatic 55 0.037
576
P HYP076 Hyperthyroidism 54 0.037
577
P PSR002 Psoriasis 54 0.037
578
CMP002 Campylobacteriosis 54 0.037
579
c JBR020 Joubert Syndrome 1 54 0.037
580
VGT001 Vogt-Koyanagi-Harada Disease 53 0.037
581
P CNJ013 Conjunctivitis 53 0.037
582
CHL067 Cholecystitis 53 0.037
583
MLG108 Malignant Melanoma, Somatic 52 0.037
584
TST021 Testicular Germ Cell Tumor 51 0.037
585
P MTH007 Methemoglobinemia 51 0.037
586
P CRT033 Corticobasal Degeneration 51 0.037
587
MSM014 Mismatch Repair Cancer Syndrome 51 0.037
588
NDL013 Nodular Regenerative Hyperplasia 51 0.037
589
GLB015 Glioblastoma Multiforme 51 0.037
590
P SCL015 Scleritis 50 0.037
591
INT054 Intraocular Lymphoma 50 0.037
592
THY022 Thymic Carcinoma 50 0.037
593
CLS007 Classic Kaposi Sarcoma 49 0.037
594
P SDR002 Siderosis 49 0.037
595
c CNT016 Central Retinal Vein Occlusion 49 0.037
596
LST001 Listeriosis 49 0.037
597
BRN029 Brain Disease 49 0.037
598
ILT001 Ileitis 49 0.037
599
EPD001 Epidermodysplasia Verruciformis 49 0.037
600
P SML034 Small Cell Neuroendocrine Carcinoma 49 0.037
601
BLS002 Blastomycosis 48 0.037
602
HST009 Histiocytoma 46 0.037
603
FBR003 Fibrous Histiocytoma 46 0.037
604
HNT002 Hantavirus Pulmonary Syndrome 46 0.037
605
SPT004 Septic Arthritis 45 0.037
606
P LYM025 Lymphedema 45 0.037
607
ACT008 Actinic Keratosis 45 0.037
608
TRP014 Triploidy 45 0.037
609
STN007 Stenotrophomonas Maltophilia 45 0.037
610
FRZ001 Frozen Shoulder 45 0.037
611
CLC006 Calcinosis 44 0.037
612
WBR001 Weber Syndrome 44 0.037
613
P LTR001 Lateral Sclerosis 43 0.037
614
c PRM012 Primary Polycythemia 43 0.037
615
GST027 Gastric Lymphoma 42 0.037
616
MCR020 Microsporidiosis 42 0.037
617
OVR012 Ovarian Serous Cystadenocarcinoma 42 0.037
618
GNG002 Ganglioneuroma 42 0.037
619
PDT021 Pediatric Osteosarcoma 41 0.037
620
PLR008 Pleurisy 41 0.037
621
SGT001 Sagittal Sinus Thrombosis 40 0.037
622
SPL004 Splenic Marginal Zone Lymphoma 40 0.037
623
PRP016 Paraplegia 40 0.037
624
MLN057 Melanoma of Soft Parts 40 0.037
625
OLG015 Oligoarticular Juvenile Arthritis 39 0.037
626
MCR017 Macrocytic Anemia 38 0.037
627
DBT087 Diabetes Insipidus, Neurohypophyseal 38 0.037
628
c LSS005 Lissencephaly 1 37 0.037
629
P FNC044 Fanconi Anemia, Complementation Group C 37 0.037
630
PRM097 Primary Immunodeficiency Disease 36 0.037
631
JBR006 Joubert Syndrome with Oculorenal Anomalies 36 0.037
632
MYC017 Mycobacterium Kansasii 35 0.037
633
HPT002 Hepatic Vein Thrombosis 35 0.037
634
APH002 Aphasia 35 0.037
635
MNN002 Mononeuritis Multiplex 33 0.037
636
MSN004 Mesenchymal Cell Neoplasm 31 0.037
637
PSL001 Pasli Disease 30 0.037
638
MYL045 Myelofibrosis with Myeloid Metaplasia, Somatic 29 0.037
639
NRG004 Neurogenic Diabetes Insipidus 25 0.037
640
IMM001 Immune-Complex Glomerulonephritis 23 0.037
641
EXF003 Exfoliative Dermatitis 21 0.037
642
c SPS042 Spastic Paraplegia 9 21 0.037
643
OBS063 Obesity, Morbid, Due to Leptin Deficiency 20 0.037
644
HYP179 Hypertrichosis Congenital Generalized X-Linked 20 0.037
645
ORB012 Orbital Cancer 20 0.037
646
ALD004 Ala Dehydratase Deficiency 11 0.037
647
P AST005 Asthma 84 0.034
648
MLR004 Malaria 81 0.034
649
P HRD008 Hereditary Hemorrhagic Telangiectasia 75 0.034
650
SCK003 Sickle Cell Anemia 70 0.034
651
KPS004 Kaposi Sarcoma 68 0.034
652
CHR012 Chronic Granulomatous Disease 64 0.034
653
P MYS003 Myasthenia Gravis 64 0.034
654
c MLT136 Multiple Endocrine Neoplasia 1 63 0.034
655
LSH001 Leishmaniasis 63 0.034
656
P DRM010 Dermatomyositis 62 0.034
657
P LVR013 Liver Disease 62 0.034
658
PRT036 Peritonitis 61 0.034
659
CHR003 Cherubism 60 0.034
660
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 59 0.034
661
P STM004 Stomach Cancer 59 0.034
662
THR016 Thrombophlebitis 58 0.034
663
GSG001 Gas Gangrene 58 0.034
664
PLS006 Plasmodium Vivax Malaria 57 0.034
665
ACT049 Acute Disseminated Encephalomyelitis 57 0.034
666
GST023 Gastric Ulcer 57 0.034
667
END030 End Stage Renal Failure 56 0.034
668
GRV001 Graves' Disease 54 0.034
669
GRY002 Gray Platelet Syndrome 54 0.034
670
P MSC005 Muscular Dystrophy 54 0.034
671
CRY003 Cryptosporidiosis 53 0.034
672
P RBL001 Rubella 53 0.034
673
TYP007 Typhoid Fever 53 0.034
674
c MNN043 Meningioma, Familial 53 0.034
675
P THR005 Thrombotic Thrombocytopenic Purpura 53 0.034
676
GLS001 Gliosarcoma 52 0.034
677
c ATM011 Autoimmune Hepatitis 51 0.034
678
EXF001 Exfoliation Syndrome 51 0.034
679
SPN020 Spondylosis 51 0.034
680
CHC001 Chickenpox 51 0.034
681
P PRM011 Primary Ciliary Dyskinesia 51 0.034
682
ALP008 Alopecia 51 0.034
683
CHR074 Choriocarcinoma 50 0.034
684
P PLC011 Pilocytic Astrocytoma 49 0.034
685
AMN001 Amenorrhea 49 0.034
686
P PRT013 Portal Hypertension 49 0.034
687
ANR004 Anuria 48 0.034
688
P HRD001 Hereditary Multiple Exostoses 48 0.034
689
P RTN022 Retinal Vein Occlusion 48 0.034
690
DWR001 Dwarfism 48 0.034
691
P CMP008 Compartment Syndrome 47 0.034
692
P HYP014 Hyperuricemia 47 0.034
693
RDC002 Radiculopathy 47 0.034
694
SHW004 Shwachman-Bodian-Diamond Syndrome 47 0.034
695
P MNT147 Mental Retardation 46 0.034
696
PNM001 Pneumocystosis 46 0.034
697
PTT004 Pituitary Apoplexy 46 0.034
698
MLT001 Multiple Chemical Sensitivity 46 0.034
699
PPL021 Papilledema 46 0.034
700
P PRN022 Perineurioma 45 0.034
701
DFF019 Diffuse Gastric Cancer 45 0.034
702
HYP037 Hyperhomocysteinemia 45 0.034
703
c HPT007 Hepatitis E 45 0.034
704
c INT072 Intestinal Pseudo-Obstruction 44 0.034
705
c CNG027 Congenital Hemolytic Anemia 44 0.034
706
P AGM005 Agammaglobulinemia, X-Linked 1 44 0.034
707
OLG006 Oligoastrocytoma 44 0.034
708
SCH063 Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic 44 0.034
709
P DRR001 Diarrhea 44 0.034
710
ERY003 Erythema Multiforme 44 0.034
711
LYM052 Lymphomatoid Papulosis 43 0.034
712
CRB090 Cerebral Hypoxia 43 0.034
713
ORC001 Orchitis 43 0.034
714
HYP068 Hyperostosis 43 0.034
715
STM007 Stomatitis 43 0.034
716
ASB001 Asbestosis 42 0.034
717
END021 Endomyocardial Fibrosis 42 0.034
718
LMB024 Limbic Encephalitis 42 0.034
719
GST014 Gastrointestinal Lymphoma 42 0.034
720
CWP001 Cowpox 42 0.034
721
PRN029 Parainfluenza Virus Type 3 41 0.034
722
c THR092 Thrombophilia Due to Thrombin Defect 41 0.034
723
CHY006 Chylous Ascites 40 0.034
724
CRY001 Cryptogenic Organizing Pneumonia 40 0.034
725
DRM011 Dermatophytosis 40 0.034
726
PRT038 Protein-Energy Malnutrition 40 0.034
727
P PTS002 Ptosis 39 0.034
728
FSC004 Fasciitis 39 0.034
729
c HRD086 Hereditary Hypophosphatemic Rickets 39 0.034
730
MCP006 Mucoepidermoid Carcinoma 39 0.034
731
MCR037 Macroglossia 38 0.034
732
INT067 Interstitial Nephritis 38 0.034
733
GND001 Gonadoblastoma 37 0.034
734
CHR276 Chronic Active Epstein-Barr Virus Infection 37 0.034
735
SNL007 Senile Cataract 36 0.034
736
THR100 Thrombocytopenic Purpura, Autoimmune 35 0.034
737
ERY045 Erythrocytosis, Somatic 35 0.034
738
c HYD008 Hydrocephalus Due to Aqueductal Stenosis 35 0.034
739
CDQ001 Cauda Equina Syndrome 35 0.034
740
FBR002 Fibrosarcoma of Bone 34 0.034
741
PRM014 Periampullary Adenocarcinoma 34 0.034
742
SBC024 Subcutaneous Panniculitis-Like T-Cell Lymphoma 33 0.034
743
PHH001 Phaeohyphomycosis 32 0.034
744
c PSD047 Pseudo-Turner Syndrome 31 0.034
745
P EPS030 Episodic Kinesigenic Dyskinesia 1 31 0.034
746
DST056 Distal 22q11.2 Microdeletion Syndrome 31 0.034
747
c SYS043 Systemic Lupus Erythematosus 1 30 0.034
748
CHR020 Chronic Interstitial Cystitis 30 0.034
749
ANM001 Anemia of Prematurity 29 0.034
750
PLY010 Polyclonal Hypergammaglobulinemia 29 0.034
751
NTR005 Nutritional Deficiency Disease 28 0.034
752
P CRN035 Cranial Nerve Palsy 26 0.034
753
c CNG023 Congenital Fibrosarcoma 26 0.034
754
MLG041 Malignant Triton Tumor 26 0.034
755
LNG004 Langerhans Cell Sarcoma 25 0.034
756
ANP008 Anaplastic Oligoastrocytoma 24 0.034
757
MLN012 Melanoma and Neural System Tumor Syndrome 24 0.034
758
PRR008 Periarteritis Nodosa 23 0.034
759
SML025 Small Non-Cleaved Cell Lymphoma 17 0.034
760
HRD137 Hereditary Isolated Aplastic Anemia 17 0.034
761
BLD053 Blood Platelet Disease 17 0.034
762
IND005 Indolent B Cell Lymphoma 16 0.034
763
CD3004 Cd3epsilon Deficiency 15 0.034
764
CYT018 Cytochrome P450 2d6 Variant 15 0.034
765
HHV001 Hhv-6 Encephalitis 14 0.034
766
CHR257 Chromosome 6q Deletion 14 0.034
767
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 82 0.030
768
P SCH015 Schizophrenia 79 0.030
769
DCH001 Duchenne Muscular Dystrophy 78 0.030
770
ADN021 Adenomatous Polyposis Coli 75 0.030
771
PHN003 Phenylketonuria 73 0.030
772
c HMP004 Hemophilia B 72 0.030
773
P LPR003 Leprosy 71 0.030
774
P OST002 Osteoporosis 71 0.030
775
FCT007 Factor Vii Deficiency 70 0.030
776
P CLD001 Cleidocranial Dysplasia 70 0.030
777
P CLC005 Celiac Disease 69 0.030
778
P WSK001 Wiskott-Aldrich Syndrome 69 0.030
779
ACR007 Acromegaly 69 0.030
780
CNG034 Congestive Heart Failure 69 0.030
781
P ALX003 Alexander Disease 66 0.030
782
CHD001 Chediak-Higashi Syndrome 66 0.030
783
KWS002 Kawasaki Disease 66 0.030
784
P OST001 Osteopetrosis 65 0.030
785
CCC001 Coccidioidomycosis 63 0.030
786
RLP001 Relapsing Polychondritis 63 0.030
787
P CNG401 Congenital Heart Disease 62 0.030
788
PRP027 Peripheral Vascular Disease 60 0.030
789
ALC007 Alcohol Dependence 60 0.030
790
P DYS007 Dyskeratosis Congenita 60 0.030
791
BLL006 Bullous Pemphigoid 60 0.030
792
KRT004 Keratitis 60 0.030
793
PBL001 Piebaldism 59 0.030
794
c MLG068 Malignant Glioma 58 0.030
795
c MTB001 Metabolic Syndrome X 58 0.030
796
ACN011 Acne 58 0.030
797
OMN001 Omenn Syndrome 58 0.030
798
P TRN020 Turner Syndrome 58 0.030
799
CRY005 Cryptococcosis 58 0.030
800
P THR015 Thrombophilia 57 0.030
801
GNT003 Genital Herpes 57 0.030
802
ALP001 Alopecia Universalis 57 0.030
803
DBN001 Dubin-Johnson Syndrome 57 0.030
804
CDL003 Caudal Regression Syndrome 57 0.030
805
P ERY008 Erythromelalgia 56 0.030
806
PMS001 Poems Syndrome 56 0.030
807
P ALP009 Alopecia Areata 56 0.030
808
MXD005 Mixed Connective Tissue Disease 56 0.030
809
PRT014 Protein S Deficiency 55 0.030
810
THY095 Thyroid Carcinoma, Follicular 55 0.030
811
LBR002 Leber Hereditary Optic Neuropathy 55 0.030
812
ACR008 Acrocallosal Syndrome 55 0.030
813
P RHN004 Rhinitis 54 0.030
814
LYM009 Lymphocytic Choriomeningitis 54 0.030
815
HYD012 Hydrops Fetalis 53 0.030
816
ISC004 Ischemia 53 0.030
817
RBR001 Roberts Syndrome 53 0.030
818
P ADL010 Adult Respiratory Distress Syndrome 53 0.030
819
RSD004 Rosai-Dorfman Disease 53 0.030
820
TST014 Testicular Cancer 53 0.030
821
ASP003 Aseptic Meningitis 52 0.030
822
P LRY016 Laryngeal Carcinoma 51 0.030
823
P ANG015 Angioedema 51 0.030
824
P GLY013 Glycogen Storage Disease 51 0.030
825
c CNG124 Congenital Rubella 51 0.030
826
SYN007 Synovitis 51 0.030
827
c HPT003 Hepatitis a 51 0.030
828
VSC003 Visceral Leishmaniasis 50 0.030
829
EMP007 Emphysema Due to Aat Deficiency 50 0.030
830
PRL009 Prolactinoma 50 0.030
831
TBR011 Tuberculous Meningitis 50 0.030
832
P CTR002 Cataract 50 0.030
833
SLD003 Sialadenitis 50 0.030
834
PRP025 Peripheral Primitive Neuroectodermal Tumor 50 0.030
835
EPD053 Epidermal Nevus, Somatic 50 0.030
836
CNN005 Connective Tissue Disease 50 0.030
837
P MYC008 Myocarditis 50 0.030
838
c XRD012 Xeroderma Pigmentosum, Group D 50 0.030
839
HYP024 Hypoparathyroidism 48 0.030
840
PPL049 Papillon-Lefevre Syndrome 48 0.030
841
ANH002 Anhidrosis 48 0.030
842
SPN051 Spondylitis 48 0.030
843
P CHR019 Choroid Plexus Carcinoma 48 0.030
844
P GNT008 Giant Cell Tumor 47 0.030
845
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 47 0.030
846
P OPH004 Ophthalmoplegia 47 0.030
847
TNG009 Tongue Squamous Cell Carcinoma 47 0.030
848
PRT018 Portal Vein Thrombosis 47 0.030
849
ACR005 Acrodermatitis 47 0.030
850
LMB002 Lambert-Eaton Myasthenic Syndrome 47 0.030
851
PRT019 Protein-Losing Enteropathy 47 0.030
852
ATY008 Atypical Lipomatous Tumor 46 0.030
853
TTH006 Tooth Disease 46 0.030
854
PTS001 Patau Syndrome 46 0.030
855
PTT037 Pituitary Tumors 46 0.030
856
JNT002 Joint Disorders 46 0.030
857
MYL001 Myelitis 46 0.030
858
c PST022 Posterior Uveal Melanoma 46 0.030
859
PLY013 Polymyalgia Rheumatica 45 0.030
860
c ANT034 Anterior Uveitis 45 0.030
861
TNG003 Tongue Cancer 45 0.030
862
GST060 Gastric Cancer, Somatic 45 0.030
863
JVN033 Juvenile Nasopharyngeal Angiofibroma 45 0.030
864
PNV001 Panuveitis 45 0.030
865
DBT006 Diabetic Macular Edema 45 0.030
866
NM001 Noma 44 0.030
867
FCT005 Factor Xiii Deficiency 44 0.030
868
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 44 0.030
869
GNG012 Gingival Overgrowth 44 0.030
870
EMP001 Empty Sella Syndrome 44 0.030
871
MLK003 Melkersson-Rosenthal Syndrome 44 0.030
872
PLS009 Plasma Cell Neoplasm 44 0.030
873
CHL028 Childhood Type Dermatomyositis 43 0.030
874
GNT031 Genitopatellar Syndrome 43 0.030
875
P BRY001 Berylliosis 43 0.030
876
P PLG001 Pelger-Huet Anomaly 43 0.030
877
GLS007 Glossitis 43 0.030
878
c ACQ012 Acquired Angioedema 43 0.030
879
P CYS018 Cystitis 43 0.030
880
LPD004 Lipoid Nephrosis 43 0.030
881
MDT001 Mediterranean Spotted Fever 43 0.030
882
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 43 0.030
883
INT075 Intracranial Hypertension 43 0.030
884
P CST002 Castleman's Disease 42 0.030
885
BRN018 Borna Disease 42 0.030
886
INF058 Inflammatory Myofibroblastic Tumor 42 0.030
887
PYG006 Pyogenic Granuloma 42 0.030
888
SPN032 Spindle Cell Carcinoma 42 0.030
889
TXC002 Toxic Encephalopathy 42 0.030
890
NPH003 Nephrocalcinosis 41 0.030
891
ANL011 Anal Canal Carcinoma 41 0.030
892
RTN003 Retinal Ischemia 40 0.030
893
TNS001 Tenosynovial Giant Cell Tumor 40 0.030
894
ACT167 Acute Generalized Exanthematous Pustulosis 40 0.030
895
P ART084 Arteriovenous Fistula 40 0.030
896
BLT006 Bilateral Breast Cancer 40 0.030
897
MTG002 Mutagen Sensitivity 40 0.030
898
GNG008 Ganglioneuroblastoma 40 0.030
899
P ATM019 Autoimmune Polyendocrine Syndrome 40 0.030
900
MMB002 Membranous Glomerulonephritis 40 0.030
901
c GMM003 Gamma Heavy Chain Disease 39 0.030
902
GRD007 Grade Iii Astrocytoma 39 0.030
903
P BRS044 Breast Adenocarcinoma 39 0.030
904
CNT025 Central Pontine Myelinolysis 39 0.030
905
MXL004 Maxillary Sinus Squamous Cell Carcinoma 39 0.030
906
c CHR048 Chronic Rhinitis 39 0.030
907
MNN009 Meningoencephalitis 39 0.030
908
P NRL007 Neurologic Diseases 39 0.030
909
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 38 0.030
910
FST010 Fasting Hypoglycemia 38 0.030
911
NCR007 Necrotizing Fasciitis 38 0.030
912
P TRC005 Tracheal Stenosis 37 0.030
913
MYC019 Mycobacterium Marinum 37 0.030
914
c INF069 Infantile Neuroaxonal Dystrophy 1 36 0.030
915
NPH017 Nephrosis 36 0.030
916
TRT001 Teratocarcinoma 36 0.030
917
TRN060 Truncus Arteriosus 36 0.030
918
P OTT001 Otitis Externa 35 0.030
919
P CNG003 Congenital Dyserythropoietic Anemia 35 0.030
920
PLN006 Poland Syndrome 35 0.030
921
WRN003 Wernicke Encephalopathy 35 0.030
922
P DCR003 Dacryoadenitis 35 0.030
923
CRB085 Cerebral Hemorrhage 35 0.030
924
IMM033 Immunodeficiency Due to Purine Nucleoside Phosphorylase Deficiency 34 0.030
925
ACL001 Acalculous Cholecystitis 34 0.030
926
P HVY001 Heavy Chain Disease 33 0.030
927
PTY004 Pityriasis Lichenoides 33 0.030
928
GMM002 Gamma Chain Deficiency 33 0.030
929
PRD019 Periodic Fever, Familial 33 0.030
930
GST012 Gastroesophageal Junction Adenocarcinoma 33 0.030
931
UNL002 Unilateral Retinoblastoma 33 0.030
932
c SYS007 Systemic Capillary Leak Syndrome 32 0.030
933
ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 32 0.030
934
GNG006 Gingival Hypertrophy 32 0.030
935
CHR208 Chromosome 17p Deletion 32 0.030
936
c RNG004 Ring Chromosome 1 32 0.030
937
GTT002 Guttate Psoriasis 31 0.030
938
KLD001 Keloids 31 0.030
939
HYP299 Hyperostosis, Endosteal 30 0.030
940
CYL004 Cylindromatosis, Familial 30 0.030
941
PLM074 Pulmonary Function 30 0.030
942
NCR009 Necrobiotic Xanthogranuloma 30 0.030
943
CHR415 Chronic Venous Leg Ulcers 29 0.030
944
c ACQ010 Acquired Polycythemia 29 0.030
945
GRN009 Granulomatous Hepatitis 29 0.030
946
DYS012 Dyshidrosis 28 0.030
947
OBS062 Obesity, Morbid, Due to Leptin Receptor Deficiency 28 0.030
948
ENG004 Engraftment Syndrome 28 0.030
949
c NTR038 Neutropenia, Severe Congenital 3, Autosomal Recessive 28 0.030
950
ORL019 Oral Hairy Leukoplakia 28 0.030
951
PLY021 Polyradiculopathy 27 0.030
952
CRV036 Cervical Carcinosarcoma 26 0.030
953
CHL040 Cholangiolocellular Carcinoma 26 0.030
954
EPD018 Epididymo-Orchitis 26 0.030
955
MYL015 Myeloproliferative Disorder with Eosinophilia 25 0.030
956
IDP021 Idiopathic Myopathy 25 0.030
957
LCH007 Lichen Planus Follicularis 25 0.030
958
NNL001 Non-Langerhans-Cell Histiocytosis 22 0.030
959
P SKN013 Skin Benign Neoplasm 22 0.030
960
TRN028 Transient Acantholytic Dermatosis 21 0.030
961
c IRD008 Iridogoniodysgenesis, Type 2 21 0.030
962
BLN009 Balanoposthitis 21 0.030
963
EMB016 Emberger Syndrome 20 0.030
964
c MLG036 Malignant Spiradenoma 20 0.030
965
6MR001 6-Mercaptopurine Sensitivity 20 0.030
966
P BKV001 Bk-Virus Nephropathy 20 0.030
967
CRT009 Critical Illness Polyneuropathy 19 0.030
968
PRK066 Parkinsonism with Spasticity, X-Linked 19 0.030
969
CHR463 Chronic Actinic Dermatitis 19 0.030
970
VRS001 Virus Associated Hemophagocytic Syndrome 18 0.030
971
DMD001 Demodicidosis 18 0.030
972
EXT039 Extrapontine Myelinolysis 17 0.030
973
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 17 0.030
974
c IRD006 Iridogoniodysgenesis, Dominant Type 16 0.030
975
c RNG024 Ring Chromosome 8 16 0.030
976
SPL009 Splenic Sequestration 16 0.030
977
NTR013 Neutropenia, Nonimmune Chronic Idiopathic, of Adults 16 0.030
978
c TRN063 Transient Myeloproliferative Syndrome 10 0.030
979
CYS001 Cystic Fibrosis 92 0.026
980
P PNC035 Pancreatic Cancer 82 0.026
981
NRL016 Neural Tube Defects 78 0.026
982
P SCL016 Scleroderma 76 0.026
983
WLS001 Wilson Disease 74 0.026
984
CDS001 Cadasil 73 0.026
985
ACH004 Achondroplasia 68 0.026
986
P TBR001 Tuberous Sclerosis 68 0.026
987
ESP021 Esophageal Cancer 67 0.026
988
P CYS013 Cystinuria 67 0.026
989
c HMP029 Hemophilia a 66 0.026
990
STR067 Stroke, Ischemic 65 0.026
991
P BRD002 Bardet-Biedl Syndrome 65 0.026
992
MNK001 Menkes Disease 65 0.026
993
MGR002 Migraine 64 0.026
994
c MCP003 Mucopolysaccharidosis Vii 64 0.026
995
PCK002 Pick Disease 64 0.026
996
CFF002 Coffin-Lowry Syndrome 63 0.026
997
ATT013 Attention Deficit-Hyperactivity Disorder 63 0.026
998
P NMN002 Niemann-Pick Disease 63 0.026
999
MCK007 Muckle-Wells Syndrome 62 0.026
1000
ART016 Aortic Aneurysm 62 0.026
1001
WRN001 Werner Syndrome 62 0.026
1002
BRN024 Bronchitis 62 0.026
1003
MLD001 Melioidosis 62 0.026
1004
P LNG028 Long Qt Syndrome 62 0.026
1005
LPP001 Lipoprotein Lipase Deficiency 61 0.026
1006
P VLC001 Velocardiofacial Syndrome 60 0.026
1007
BLS001 Blau Syndrome 60 0.026
1008
PLY017 Polyarteritis Nodosa 60 0.026
1009
P HYP086 Hypothyroidism 59 0.026
1010
P PRD008 Periodontitis 59 0.026
1011
LMY002 Leiomyoma 59 0.026
1012
P END044 Endometriosis 59 0.026
1013
P RCK004 Rickets 58 0.026
1014
FCT003 Factor X Deficiency 58 0.026
1015
ALC006 Alcoholic Hepatitis 58 0.026
1016
ALS001 Alstrom Syndrome 58 0.026
1017
ERD001 Erdheim-Chester Disease 58 0.026
1018
P SLV001 Silver-Russell Syndrome 57 0.026
1019
c SML001 Small Cell Carcinoma 57 0.026
1020
PHR003 Pharyngitis 56 0.026
1021
P GST044 Gastritis 56 0.026
1022
P TXP001 Toxoplasmosis 56 0.026
1023
P DRM007 Dermatitis Herpetiformis 56 0.026
1024
TRG002 Trigeminal Neuralgia 56 0.026
1025
CHL014 Cholera 56 0.026
1026
P BRG001 Brugada Syndrome 56 0.026
1027
P MCP010 Mucopolysaccharidosis 56 0.026
1028
INT146 Intervertebral Disc Disease 55 0.026
1029
GLB001 Gilbert Syndrome 55 0.026
1030
c XRD019 Xeroderma Pigmentosum, Group C 55 0.026
1031
ATP002 Atopy 55 0.026
1032
c VRL010 Viral Hepatitis 54 0.026
1033
P RHB017 Rhabdoid Tumor 54 0.026
1034
PRT037 Pertussis 54 0.026
1035
CHG001 Chagas Disease 54 0.026
1036
TTN003 Tetanus 54 0.026
1037
CRN036 Craniopharyngioma 54 0.026
1038
EXT034 Extrinsic Allergic Alveolitis 54 0.026
1039
P PRC019 Precocious Puberty 53 0.026
1040
P KDN017 Kidney Cancer 53 0.026
1041
OLL001 Ollier Disease 53 0.026
1042
PLM014 Pleomorphic Adenoma 53 0.026
1043
P INT070 Intestinal Obstruction 53 0.026
1044
APP015 Apparent Mineralocorticoid Excess 53 0.026
1045
BRC012 Brucellosis 53 0.026
1046
MCK005 Mckusick-Kaufman Syndrome 52 0.026
1047
P MCK022 Meckel Syndrome 1 52 0.026
1048
PTT006 Pituitary Adenoma 52 0.026
1049
ACR003 Acrodermatitis Enteropathica 52 0.026
1050
ICH002 Ichthyosis Bullosa of Siemens 52 0.026
1051
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.026
1052
DBT001 Diabetic Ketoacidosis 52 0.026
1053
MCR013 Microphthalmia 52 0.026
1054
STT002 Status Asthmaticus 52 0.026
1055
P HYP141 Hyperphenylalaninemia 51 0.026
1056
c SCN006 Secondary Syphilis 51 0.026
1057
MLT075 Multifocal Motor Neuropathy 51 0.026