Search results for Fludarabine

1574 hits were found for Fludarabine

# Family MCID Name MIFTS Score
1
P LKM002 Leukemia 71 0.323
2
c CHR090 Chronic Lymphocytic Leukemia 76 0.271
3
c CHR418 Chronic Leukemia 47 0.220
4
P LYM118 Lymphoma 69 0.208
5
P LYM026 Lymphoblastic Leukemia 62 0.207
6
BNM001 Bone Marrow Cancer 51 0.206
7
LYM067 Lymphoid Leukemia 44 0.206
8
LYM023 Lymphatic System Cancer 33 0.203
9
P LYM033 Lymphoproliferative Syndrome 56 0.200
10
MRG013 Mirage Syndrome 29 0.199
11
P MYL006 Myeloid Leukemia 66 0.191
12
c LKM004 Leukemia, B-Cell, Chronic 24 0.190
13
c ACT073 Acute Leukemia 60 0.189
14
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.189
15
HMT018 Hematopoietic Stem Cell Transplantation 41 0.187
16
LYM024 Lymphatic System Disease 52 0.185
17
c LKM056 Leukemia, Chronic Lymphocytic 2 21 0.184
18
PRM243 Primary Bone Cancer 29 0.179
19
BNC003 Bone Cancer 58 0.177
20
MYL009 Myelodysplastic Syndrome 73 0.176
21
c LKM050 Leukemia, Chronic Lymphocytic 1 19 0.175
22
c CHR064 Chronic Monocytic Leukemia 42 0.171
23
ACT118 Acute Non Lymphoblastic Leukemia 30 0.171
24
c LKM061 Leukemia, Acute Myeloid 73 0.167
25
LYM019 Lymphosarcoma 53 0.167
26
c ADL001 Adult Lymphoma 39 0.167
27
c LKM051 Leukemia, Chronic Lymphocytic 3 19 0.165
28
HMT002 Hematologic Cancer 64 0.160
29
c PRM023 Pre-Malignant Neoplasm 41 0.154
30
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.147
31
LYM115 Lymphoma, Non-Hodgkin 63 0.145
32
P ACT135 Acute Graft Versus Host Disease 53 0.145
33
P LKM068 Leukemia, Chronic Myeloid, Somatic 68 0.143
34
c CHR417 Chronic Graft Versus Host Disease 51 0.142
35
P CHR562 Chronic Myelocytic Leukemia 41 0.142
36
INC022 Inclusion-Cell Disease 46 0.139
37
GRF001 Graft-Versus-Host Disease, Protection Against 52 0.138
38
HML018 Homologous Wasting Disease 13 0.138
39
P BCL006 B-Cell Lymphomas 65 0.137
40
c ACT020 Acute T Cell Leukemia 35 0.136
41
CHL071 Child Syndrome 58 0.134
42
KDS001 Kid Syndrome 53 0.134
43
RFR004 Refractory Hematologic Cancer 28 0.134
44
P FLL037 Follicular Lymphoma 70 0.132
45
MYL031 Myeloproliferative Neoplasm 58 0.131
46
P ACT074 Acute Lymphocytic Leukemia 56 0.131
47
c LKM062 Leukemia, Acute Lymphoblastic 64 0.130
48
PLS009 Plasma Cell Neoplasm 48 0.130
49
c ADL052 Adult Acute Lymphocytic Leukemia 44 0.130
50
BNS002 Bone Structure Disease 37 0.129
51
BNL002 Bone Lymphoma 32 0.128
52
OCL009 Ocular Cancer 59 0.126
53
MCR004 Macroglobulinemia 50 0.123
54
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 32 0.123
55
c LKM055 Leukemia, Acute Lymphoblastic 2 19 0.123
56
P MLT019 Multiple Myeloma 83 0.120
57
P HMR003 Hemorrhagic Disease 57 0.120
58
BLD053 Blood Platelet Disease 46 0.120
59
BLD054 Blood Protein Disease 37 0.120
60
VSC006 Vascular Cancer 51 0.118
61
MYL004 Myelodysplastic Myeloproliferative Cancer 45 0.118
62
P BLD051 Blood Coagulation Disease 42 0.118
63
CLL014 Cll/sll 42 0.118
64
VSC008 Vascular Hemostatic Disease 30 0.118
65
P TCL004 T-Cell Leukemia 47 0.117
66
CRD118 Cardiovascular Cancer 44 0.117
67
PLS016 Plasma Cell Leukemia 42 0.117
68
PRM151 Primary Bone Lymphoma 26 0.117
69
DFC004 Deficiency Anemia 64 0.116
70
c ADL017 Adult T-Cell Leukemia 60 0.116
71
c CLL013 Cell Type Cancer 46 0.116
72
c FLL041 Follicular Lymphoma 1 45 0.116
73
c LYM107 Lymphoproliferative Syndrome 2 50 0.115
74
MNT001 Mantle Cell Lymphoma 72 0.114
75
ACD009 Acid-Labile Subunit, Deficiency of 45 0.114
76
LYM040 Lymphoblastic Lymphoma 53 0.113
77
LKC003 Leukocyte Disease 43 0.113
78
c LYM106 Lymphoproliferative Syndrome 1 32 0.113
79
ACT228 Acute Radiation Syndrome 20 0.113
80
c LKM005 Leukemia, T-Cell, Chronic 20 0.111
81
WLL006 Wells Syndrome 59 0.109
82
c LKM060 Leukemia, Acute Lymphoblastic 3 50 0.109
83
GDS001 Good Syndrome 44 0.109
84
P APL001 Aplastic Anemia 75 0.108
85
ENG004 Engraftment Syndrome 32 0.108
86
PLS003 Plasmacytic Leukemia 21 0.108
87
RFR001 Refractory Plasma Cell Neoplasm 16 0.106
88
MRG003 Marginal Zone B-Cell Lymphoma 52 0.105
89
CHL061 Childhood Leukemia 49 0.105
90
MXD023 Mixed Cell Type Cancer 44 0.105
91
LYM012 Lymphoplasmacytic Lymphoma 44 0.104
92
LYM104 Lymphoma, Malt, Somatic 54 0.103
93
HDG012 Hodgkin Lymphoma 77 0.101
94
P WLD002 Waldenstrom Macroglobulinemia 58 0.100
95
BCL012 B-Cell Lymphoma of Mucosa-Associated Lymphoid Tissue 37 0.100
96
c BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.100
97
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 15 0.099
98
DFF005 Diffuse Large B-Cell Lymphoma 59 0.097
99
C3D001 C3 Deficiency 53 0.097
100
IMM136 Immune System Disease 51 0.097
101
VSC001 Vascular Myelopathy 23 0.097
102
SPL012 Splenic Disease 46 0.096
103
SPL004 Splenic Marginal Zone Lymphoma 44 0.096
104
SPL011 Spleen Cancer 36 0.096
105
NDL020 Nodal Marginal Zone B-Cell Lymphoma 35 0.096
106
c MCR161 Macroglobulinemia, Waldenstrom 1 27 0.096
107
c MCR162 Macroglobulinemia, Waldenstrom 2 17 0.096
108
ACT184 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Alkylating Agent 13 0.096
109
ADL002 Adult Syndrome 52 0.093
110
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 24 0.093
111
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 0.091
112
HDG004 Hodgkin's Granuloma 24 0.091
113
HDG006 Hodgkin's Paragranuloma 17 0.091
114
CHR285 Chronic Myelomonocytic Leukemia 56 0.090
115
RTC005 Reticulosarcoma 48 0.090
116
RTC009 Reticulum Cell Sarcoma 47 0.090
117
LYM049 Lymphoma, Small Cleaved-Cell, Diffuse 29 0.090
118
PRP027 Peripheral Vascular Disease 68 0.088
119
ACT103 Acute Lymphoblastic Leukemia, Childhood 41 0.087
120
HRT007 Heart Cancer 46 0.085
121
P HRT017 Heart Tumor 32 0.085
122
c ADL079 Adult Heart Tumor 16 0.085
123
BRK010 Burkitt Lymphoma 69 0.084
124
P MYL005 Myelofibrosis 67 0.084
125
PLS025 Plasmablastic Lymphoma 46 0.084
126
PRP036 Peripheral T-Cell Lymphoma 45 0.084
127
BND002 B- and T-Cell Mixed Leukemia 17 0.084
128
LYM126 Lymphoma Aids Related 15 0.084
129
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.084
130
PRL017 Prolymphocytic Leukemia 47 0.082
131
PRP021 Peripheral Nervous System Neoplasm 46 0.080
132
RFR010 Refractory Anemia 45 0.080
133
LYM127 Lymphatic Malformations 39 0.080
134
ALR002 Al-Raqad Syndrome 36 0.080
135
BNM011 Bone Marrow Failure Syndrome 2 25 0.080
136
LYM048 Lymphoma, Large-Cell, Immunoblastic 25 0.080
137
ACT158 Acute Myeloid Leukemia and Myelodysplastic Syndromes Related to Radiation 12 0.080
138
PST046 Post-Transplant Lymphoproliferative Disease 54 0.079
139
VSC047 Vascular Malformation 45 0.079
140
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.079
141
DFF027 Diffuse Lymphatic Malformation 22 0.079
142
P HML002 Hemolytic Anemia 62 0.075
143
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.075
144
WHT007 White Platelet Syndrome 15 0.075
145
MYC006 Mycosis Fungoides 66 0.073
146
P KDN017 Kidney Cancer 65 0.073
147
P CTN015 Cutaneous T Cell Lymphoma 50 0.073
148
BNM010 Bone Marrow Failure Syndrome 1 29 0.073
149
c PRC004 Precursor B Lymphoblastic Lymphoma/leukemia 22 0.073
150
HRT029 Heart Tumor of the Child 15 0.073
151
P INF038 Influenza 72 0.072
152
P NRV006 Nervous System Cancer 60 0.072
153
SZR001 Sezary's Disease 52 0.072
154
VND001 Vein Disease 47 0.072
155
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.072
156
c CHR096 Chronic Pulmonary Heart Disease 40 0.072
157
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 35 0.072
158
PRM128 Primary Cutaneous Follicle Center Lymphoma 26 0.072
159
NTR003 Natural Killer Cell Leukemia 47 0.070
160
P ACT080 Acute Pulmonary Heart Disease 31 0.070
161
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 27 0.070
162
NNH003 Non-Hodgkin Lymphoma, Childhood 12 0.070
163
HRY003 Hairy Cell Leukemia 57 0.068
164
PLS011 Plasmacytoma 56 0.068
165
CSY001 C Syndrome 50 0.068
166
ATY042 Atypical Chronic Myeloid Leukemia 48 0.068
167
P BCL005 B Cell Prolymphocytic Leukemia 43 0.068
168
SNS023 Sensory System Cancer 43 0.068
169
ANP010 Anaplastic Plasmacytoma 19 0.068
170
P ANP001 Anaplastic Large Cell Lymphoma 57 0.066
171
FRB001 Farber Lipogranulomatosis 53 0.066
172
LYM051 Lymphomatoid Granulomatosis 47 0.066
173
ANG046 Angioimmunoblastic T-Cell Lymphoma 43 0.066
174
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 41 0.066
175
ARG006 Aregenerative Anemia 22 0.066
176
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 18 0.066
177
c ANP011 Anaplastic Small Cell Lymphoma 14 0.066
178
HDG009 Hodgkin Lymphoma, Childhood 14 0.066
179
NSD001 Nose Disease 48 0.064
180
ALN001 Aland Island Eye Disease 45 0.064
181
P SKN013 Skin Benign Neoplasm 43 0.064
182
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.064
183
MNC004 Monoclonal Paraproteinemia 34 0.064
184
P RFR008 Refractory Anemia with Excess Blasts 31 0.064
185
RFR002 Refractory Hairy Cell Leukemia 29 0.064
186
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 26 0.064
187
c CRN214 Coronary Heart Disease 5 22 0.064
188
TCL019 T-Cell Childhood Lymphoblastic Lymphoma 14 0.064
189
PLY125 Polycythemia Vera, Somatic 63 0.061
190
ISC004 Ischemia 61 0.061
191
P NTR004 Neutropenia 59 0.061
192
P PLY018 Polycythemia 58 0.061
193
c PRM012 Primary Polycythemia 52 0.061
194
TCL003 T Cell Deficiency 45 0.061
195
GRN017 Granulocytopenia 44 0.061
196
MCR128 Macrocytic Anemia, Refractory, Due to 5q Deletion, Somatic 39 0.061
197
LTH001 Lethal Midline Granuloma 37 0.061
198
CNT018 Central Nervous System Leukemia 37 0.061
199
PHY001 Physiological Polycythemia 28 0.061
200
BNM013 Bone Marrow Failure Syndrome 3 17 0.061
201
c RFR014 Refractory Anemia with Excess Blasts Type 2 16 0.061
202
c SML023 Small Cell Lung Cancer, Adult 15 0.061
203
CHR062 Chronic Erythremia 13 0.061
204
TST021 Testicular Germ Cell Tumor 69 0.059
205
P THR014 Thrombocytopenia 64 0.059
206
THR004 Thrombocytosis 55 0.059
207
CNG028 Congenital Hypoplastic Anemia 48 0.059
208
BRT030 Birth Defects 43 0.059
209
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.059
210
EPS006 Epstein Syndrome 38 0.059
211
ADJ001 Adjustment Disorder 38 0.059
212
SML025 Small Non-Cleaved Cell Lymphoma 22 0.059
213
c CRN173 Coronary Heart Disease 8 18 0.059
214
ACC008 Accelerated Tumor Formation 17 0.059
215
P MDL005 Medulloblastoma 77 0.057
216
EWN003 Ewing Sarcoma 66 0.057
217
P DYS007 Dyskeratosis Congenita 63 0.057
218
MLN008 Melanoma 62 0.057
219
NRN004 Neuroendocrine Tumor 56 0.057
220
c TCL005 T-Cell Prolymphocytic Leukemia 52 0.057
221
CRC006 Carcinoid Syndrome 52 0.057
222
c INH020 Inherited Metabolic Disorder 49 0.057
223
RCH001 Richter's Syndrome 45 0.057
224
TCL002 T-Cell Large Granular Lymphocyte Leukemia 42 0.057
225
LRG008 Large Granular Lymphocyte Leukemia 39 0.057
226
LNG013 Lung Lymphoma 38 0.057
227
GRM001 Germ Cell and Embryonal Cancer 36 0.057
228
NTR005 Nutritional Deficiency Disease 36 0.057
229
SLT001 Solitary Osseous Plasmacytoma 36 0.057
230
PRM133 Primary Pulmonary Lymphoma 23 0.057
231
IND005 Indolent B Cell Lymphoma 23 0.057
232
WSC001 Wisconsin Syndrome 14 0.057
233
P ESS003 Essential Thrombocythemia 70 0.054
234
c ATM010 Autoimmune Hemolytic Anemia 60 0.054
235
PRM097 Primary Immunodeficiency Disease 60 0.054
236
MLN054 Melanocytic Nevus Syndrome, Congenital, Somatic 56 0.054
237
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.054
238
P GRN010 Granular Cell Tumor 47 0.054
239
SKN023 Skin Tag 44 0.054
240
CLV009 Clove Syndrome, Somatic 41 0.054
241
HRT003 Heart Lymphoma 30 0.054
242
c THR086 Thrombocythemia 3 25 0.054
243
CNT010 Central Nervous System Hematologic Cancer 18 0.054
244
c CRN176 Coronary Heart Disease 9 18 0.054
245
c RFR015 Refractory Anemia with Excess Blasts Type 1 15 0.054
246
PRM165 Primary Plasmacytoma of the Bone 12 0.054
247
c FNC027 Fanconi Anemia, Complementation Group a 71 0.052
248
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.052
249
SKN019 Skin Melanoma 62 0.052
250
LKM066 Leukemia, Acute Myelomonocytic, Somatic, Somatic 60 0.052
251
P CNT005 Central Nervous System Lymphoma 53 0.052
252
c PRM226 Primary Central Nervous System Lymphoma 49 0.052
253
P FNC004 Fanconi Syndrome 49 0.052
254
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.052
255
HMG002 Hemoglobinuria 48 0.052
256
CHR563 Chronic Eosinophilic Leukemia 46 0.052
257
c HMN022 Human T-Cell Leukemia Virus Type 2 44 0.052
258
c THR037 Thrombocytopenia 2 35 0.052
259
c THR090 Thrombocythemia 1 30 0.052
260
c THR048 Thrombocytopenia 4 26 0.052
261
c PRM200 Primary Fanconi Syndrome 24 0.052
262
c THR110 Thrombocytopenia 6 20 0.052
263
c HMN023 Human T-Cell Leukemia Virus Type 3 14 0.052
264
P RNL014 Renal Cell Carcinoma 82 0.049
265
RNL101 Renal Cell Carcinoma, Papillary 63 0.049
266
PRR002 Pure Red-Cell Aplasia 47 0.049
267
CHR286 Chronic Neutrophilic Leukemia 43 0.049
268
RNL025 Renal Hypoplasia 42 0.049
269
CYS036 Cystinosis, Nephropathic 41 0.049
270
HPT070 Hepatosplenic T-Cell Lymphoma 39 0.049
271
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.049
272
RNL021 Renal Tubular Transport Disease 32 0.049
273
RDT005 Radiation Induced Cancer 28 0.049
274
CNT067 Central Cord Syndrome 23 0.049
275
RFR007 Refractory Anemia with Excess Blasts in Transformation 20 0.049
276
PDG001 Pdgfra-Associated Chronic Eosinophilic Leukemia 12 0.049
277
P HRT032 Heart Disease 75 0.046
278
CHR012 Chronic Granulomatous Disease 65 0.046
279
P SML001 Small Cell Carcinoma 56 0.046
280
SML033 Small Cell Cancer of the Lung, Somatic 54 0.046
281
P SML016 Small Intestine Cancer 52 0.046
282
P PNC001 Pancytopenia 52 0.046
283
INT253 Intestinal Benign Neoplasm 47 0.046
284
INT054 Intraocular Lymphoma 45 0.046
285
BND014 Bone Development Disease 40 0.046
286
ATN003 Autonomic Nervous System Neoplasm 40 0.046
287
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.046
288
ACR002 Acrocapitofemoral Dysplasia 33 0.046
289
P CHR084 Chromosomal Disease 32 0.046
290
c THR102 Thrombocytopenia 5 27 0.046
291
P CRN178 Coronary Heart Disease 6 21 0.046
292
LYM041 Lymphocytes Absent 13 0.046
293
KDN020 Kidney Cancer, Childhood 11 0.046
294
PCK002 Pick Disease 68 0.043
295
SKN016 Skin Disease 66 0.043
296
CNN005 Connective Tissue Disease 62 0.043
297
TST014 Testicular Cancer 53 0.043
298
OLV001 Olivopontocerebellar Atrophy 53 0.043
299
PRG009 Progressive Multifocal Leukoencephalopathy 52 0.043
300
NTR040 Neutropenia, Cyclic 51 0.043
301
BCL002 B Cell Deficiency 49 0.043
302
c CNG027 Congenital Hemolytic Anemia 48 0.043
303
TST015 Testicular Disease 44 0.043
304
SML008 Small Intestine Lymphoma 40 0.043
305
TST004 Testicular Lymphoma 37 0.043
306
TST003 Testicular Leukemia 31 0.043
307
c EYL003 Eye Lymphoma 30 0.043
308
c PRX067 Paroxysmal Nocturnal Hemoglobinuria 2 21 0.043
309
c RNL016 Renal Infectious Disease 20 0.043
310
c INF136 Influenza, Severe 15 0.043
311
TCL006 T Cell Immunodeficiency Primary 12 0.043
312
SML022 Small Cell Lung Cancer, Childhood 12 0.043
313
P DMN001 Diamond-Blackfan Anemia 69 0.040
314
MST017 Mast Cell Disease 50 0.040
315
LRN003 Learning Disability 49 0.040
316
MST002 Mast-Cell Leukemia 48 0.040
317
ACR041 Acromelic Frontonasal Dysostosis 45 0.040
318
MST006 Mast Syndrome 43 0.040
319
P CNN004 Connective Tissue Cancer 40 0.040
320
MST004 Mast Cell Neoplasm 40 0.040
321
c DMN023 Diamond-Blackfan Anemia 1 38 0.040
322
CYC007 Cyclic Thrombocytopenia 37 0.040
323
c DMN021 Diamond-Blackfan Anemia 6 35 0.040
324
c ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 34 0.040
325
PLS010 Plasma Protein Metabolism Disease 34 0.040
326
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.040
327
c DMN006 Diamond-Blackfan Anemia 3 29 0.040
328
IMM096 Immunodeficiency 30 27 0.040
329
c DMN028 Diamond-Blackfan Anemia 12 27 0.040
330
c DMN005 Diamond-Blackfan Anemia 2 22 0.040
331
ATM053 Autoimmune Disease 2 16 0.040
332
TST022 Testicular Cancer, Childhood 11 0.040
333
SML024 Small Intestine Cancer, Childhood 10 0.040
334
P HPT023 Hepatocellular Carcinoma 92 0.037
335
P ART022 Arthritis 75 0.037
336
P ADN016 Adenocarcinoma 69 0.037
337
P PNM007 Pneumonia 68 0.037
338
P AMY004 Amyloidosis 65 0.037
339
P THL005 Thalassemia 64 0.037
340
P HMP002 Hemophagocytic Lymphohistiocytosis 64 0.037
341
P HYP098 Hypereosinophilic Syndrome 63 0.037
342
MXD005 Mixed Connective Tissue Disease 62 0.037
343
FCT003 Factor X Deficiency 61 0.037
344
c SYS004 Systemic Mastocytosis 60 0.037
345
P INF032 Infertility 59 0.037
346
P THY102 Thyroid Cancer, Nonmedullary, 2 58 0.037
347
P MST009 Mastocytosis 56 0.037
348
CLR003 Clear Cell Adenocarcinoma 56 0.037
349
c SVR003 Severe Congenital Neutropenia 56 0.037
350
MGK001 Megakaryocytic Leukemia 55 0.037
351
P MNC007 Monocytic Leukemia 55 0.037
352
c RNL003 Renal Clear Cell Carcinoma 54 0.037
353
P RNL100 Renal Hypodysplasia/aplasia 1 53 0.037
354
CLR030 Clear Cell Renal Cell Carcinoma 53 0.037
355
LKM067 Leukemia, Acute Promyelocytic, Somatic 52 0.037
356
HMG005 Hemoglobinopathy 52 0.037
357
c ACT009 Acute Monocytic Leukemia 52 0.037
358
OCL022 Ocular Melanoma 52 0.037
359
ATR060 Atrial Standstill, Digenic 51 0.037
360
SCK005 Sickle Cell Disease 51 0.037
361
PMP001 Pemphigus 50 0.037
362
P PRM001 Primary Cutaneous Amyloidosis 50 0.037
363
c ACT071 Acute Kidney Failure 49 0.037
364
CTN014 Cutaneous Mastocytosis 49 0.037
365
c ALM001 Al Amyloidosis 49 0.037
366
LPD004 Lipoid Nephrosis 48 0.037
367
ACT098 Acute Erythroid Leukemia 47 0.037
368
SKN027 Skin Conditions 43 0.037
369
DFF001 Diffuse Cutaneous Mastocytosis 43 0.037
370
ACT200 Acute Monoblastic Leukemia 42 0.037
371
P HVY001 Heavy Chain Disease 41 0.037
372
PRN049 Paraneoplastic Pemphigus 40 0.037
373
c PRM225 Primary Thrombocytopenia 39 0.037
374
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.037
375
AMY002 Amyloid Tumor 37 0.037
376
P CNT036 Central Nervous System Germ Cell Tumor 37 0.037
377
PRM026 Primary Systemic Mycosis 36 0.037
378
SVR077 Severe Combined Immune Deficiency 36 0.037
379
ACT216 Acute Leukemia of Ambiguous Lineage 34 0.037
380
RDN001 Reading Disorder 34 0.037
381
c CNN010 Connective Tissue Benign Neoplasm 32 0.037
382
ACT095 Acute Biphenotypic Leukemia 32 0.037
383
GST014 Gastrointestinal Lymphoma 31 0.037
384
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.037
385
UND007 Undifferentiated Connective Tissue Disease 30 0.037
386
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.037
387
c DMN019 Diamond-Blackfan Anemia 4 27 0.037
388
ATM052 Autoimmune Disease 1 25 0.037
389
IMM120 Immunodeficiency 40 24 0.037
390
c ADL093 Adult Acute Monocytic Leukemia 19 0.037
391
c RNL034 Renal Cell Carcinoma 4 18 0.037
392
GLC077 Glucocorticoid Therapy, Response to 16 0.037
393
c ADL022 Adult Central Nervous System Primitive Neuroectodermal Neoplasm 15 0.037
394
ACT217 Acute Myeloid Leukemia with Recurrent Genetic Anomaly 10 0.037
395
P OVR042 Ovarian Cancer 76 0.033
396
SCK003 Sickle Cell Anemia 71 0.033
397
SVR004 Severe Combined Immunodeficiency 69 0.033
398
c CHR089 Chronic Kidney Failure 66 0.033
399
SHW002 Shwachman-Diamond Syndrome 61 0.033
400
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.033
401
P ORL007 Oral Cavity Cancer 59 0.033
402
P GLM007 Glomerulonephritis 59 0.033
403
ABL002 Ablepharon-Macrostomia Syndrome 57 0.033
404
ORL011 Oral Cancer 56 0.033
405
P OVR049 Ovarian Disease 56 0.033
406
END030 End Stage Renal Failure 55 0.033
407
RCT018 Rectal Neoplasm 54 0.033
408
NWC001 Newcastle Disease 54 0.033
409
LST001 Listeriosis 53 0.033
410
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 0.033
411
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.033
412
TTH006 Tooth Disease 52 0.033
413
CYT008 Cytomegalovirus Infection 52 0.033
414
P SPS003 Spastic Diplegia 52 0.033
415
URC002 Urea Cycle Disorder 51 0.033
416
c LRG001 Large Cell Carcinoma 51 0.033
417
MSC072 Muscle Cancer 49 0.033
418
ATN002 Autonomic Nervous System Disease 48 0.033
419
THL018 Thalassemia Major 48 0.033
420
LYM116 Lymph Node Disease 47 0.033
421
ADR038 Adermatoglyphia 46 0.033
422
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 0.033
423
OVR094 Ovarian Epithelial Cancer 43 0.033
424
CMB003 Combined T Cell and B Cell Immunodeficiency 42 0.033
425
PRD011 Proud Syndrome 42 0.033
426
PRM025 Primary Bacterial Infectious Disease 41 0.033
427
DND018 Dendritic Cell Tumor 41 0.033
428
CNV002 Conversion Disorder 41 0.033
429
RCT017 Rectal Disease 40 0.033
430
LYM020 Lymph Node Cancer 39 0.033
431
c PRM149 Primary Hypereosinophilic Syndrome 38 0.033
432
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.033
433
c OVR058 Ovarian Small Cell Carcinoma 36 0.033
434
FXF002 Fox-Fordyce Disease 36 0.033
435
WRT001 Worth's Syndrome 34 0.033
436
MYL015 Myeloproliferative Disorder with Eosinophilia 34 0.033
437
P XLN007 X-Linked Disease 34 0.033
438
CHL010 Childhood Kidney Cell Carcinoma 33 0.033
439
BRS001 Breast Lymphoma 32 0.033
440
IMM066 Immunodeficiency 9 30 0.033
441
IMM068 Immunodeficiency 8 30 0.033
442
BRW006 Brown Syndrome 29 0.033
443
c TRC078 Trichohepatoenteric Syndrome 2 29 0.033
444
INH011 Inherited Bone Marrow Failure Syndromes 27 0.033
445
c DMN029 Diamond-Blackfan Anemia 11 27 0.033
446
LVR006 Liver Lymphoma 27 0.033
447
IMM063 Immunodeficiency 15 26 0.033
448
IMM062 Immunodeficiency 11 26 0.033
449
IMM071 Immunodeficiency 12 26 0.033
450
YNG002 Young Syndrome 26 0.033
451
IMM025 Immunoglobulin a Deficiency 2 24 0.033
452
IND003 Indolent Myeloma 22 0.033
453
ATM059 Autoimmune Disease 6 22 0.033
454
MND006 Mondor Disease 21 0.033
455
c CRN177 Coronary Heart Disease 7 20 0.033
456
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 20 0.033
457
ATM054 Autoimmune Disease 3 15 0.033
458
DSS003 Disseminated Eosinophilic Collagen Disease 15 0.033
459
ATM055 Autoimmune Disease 4 15 0.033
460
MYL052 Myeloproliferative Neoplasms, Familial 15 0.033
461
PRM139 Primary Melanoma of the Central Nervous System 15 0.033
462
BNM004 Bone Marrow Failure, Familial 14 0.033
463
SPL013 Splenic Manifestation of Leukemia 14 0.033
464
CGL001 Coagulation Protein Disease 14 0.033
465
CRD004 Cardiac Granular Cell Neoplasm 12 0.033
466
c FML078 Familial Myelofibrosis 11 0.033
467
P CNG327 Congenital Epstein-Barr Virus Infection 11 0.033
468
P CLR023 Colorectal Cancer 97 0.028
469
P RHM011 Rheumatoid Arthritis 89 0.028
470
P PNC035 Pancreatic Cancer 87 0.028
471
GST053 Gastric Cancer 78 0.028
472
P WSK001 Wiskott-Aldrich Syndrome 73 0.028
473
WLS001 Wilson Disease 72 0.028
474
BRC012 Brucellosis 66 0.028
475
WLM007 Wilms Tumor Susceptibility-5 63 0.028
476
P LNG064 Lung Cancer Susceptibility 3 62 0.028
477
P PSR002 Psoriasis 61 0.028
478
P GST049 Gastrointestinal System Cancer 60 0.028
479
FLL027 Fallopian Tube Carcinoma 60 0.028
480
P DRR001 Diarrhea 60 0.028
481
RBR001 Roberts Syndrome 60 0.028
482
c CNT035 Central Nervous System Disease 60 0.028
483
c MNN043 Meningioma, Familial 59 0.028
484
P SHR029 Short Syndrome 58 0.028
485
PNC034 Pancreas Disease 58 0.028
486
c FML108 Familial Breast Cancer 57 0.028
487
WST001 West Syndrome 57 0.028
488
P SZR006 Seizure Disorder 56 0.028
489
LYM027 Lymphopenia 56 0.028
490
VRL011 Viral Infectious Disease 55 0.028
491
PRP019 Peripheral Nervous System Disease 55 0.028
492
c PRM126 Primary Peritoneal Carcinoma 54 0.028
493
SCT005 Scott Syndrome 53 0.028
494
P APL006 Aplasia Cutis Congenita 52 0.028
495
PNN001 Panniculitis 51 0.028
496
PPL002 Papillary Carcinoma 51 0.028
497
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 51 0.028
498
P RNL028 Renal Tubular Dysgenesis 51 0.028
499
STM006 Stomach Disease 50 0.028
500
HND003 Hand-Foot-Uterus Syndrome 50 0.028
501
FML038 Female Reproductive Organ Cancer 50 0.028
502
FML037 Female Breast Cancer 50 0.028
503
PRL032 Perlman Syndrome 50 0.028
504
EXT010 Extramedullary Plasmacytoma 49 0.028
505
QBC001 Quebec Platelet Disorder 48 0.028
506
FML039 Female Reproductive System Disease 48 0.028
507
PPL018 Papillary Adenocarcinoma 46 0.028
508
CRY004 Cryoglobulinemia 46 0.028
509
IPX001 Ipex Syndrome 45 0.028
510
P RPR003 Reproductive Organ Cancer 44 0.028
511
CLD007 Cold Agglutinin Disease 44 0.028
512
SPL018 Splenomegaly 44 0.028
513
c LYM114 Lymphoproliferative Syndrome, X-Linked, 2 43 0.028
514
NTR018 Neutrophilia, Hereditary 42 0.028
515
AGG002 Aggressive Systemic Mastocytosis 42 0.028
516
CRB138 Core Binding Factor Acute Myeloid Leukemia 42 0.028
517
RPR002 Reproductive System Disease 41 0.028
518
CMB023 Combined Immunodeficiency, X-Linked, Moderate 40 0.028
519
c ACT004 Acute Diarrhea 39 0.028
520
c PSR017 Psoriasis 2 37 0.028
521
WTH001 Withdrawal Disorder 37 0.028
522
c PNC106 Pancreatic Agenesis 1 37 0.028
523
ADR014 Adrenal Medulla Cancer 36 0.028
524
PRT035 Peritoneum Cancer 35 0.028
525
IMM078 Immunodeficiency 21 35 0.028
526
CHR340 Chronic Granulomatous Disease, X-Linked 35 0.028
527
FLC001 Folic Acid Deficiency Anemia 34 0.028
528
SBC024 Subcutaneous Panniculitis-Like T-Cell Lymphoma 34 0.028
529
c MYL058 Myeloproliferative Syndrome, Transient 33 0.028
530
GLB003 Globe Disease 32 0.028
531
LNG016 Lung Papillary Adenocarcinoma 32 0.028
532
FLL029 Fallopian Tube Disease 32 0.028
533
BNM005 Bone Marrow Necrosis 32 0.028
534
CLR112 Clear Cell Papillary Renal Cell Carcinoma 31 0.028
535
IMM027 Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome 31 0.028
536
c PNC095 Pancreatic Cancer 3 30 0.028
537
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 30 0.028
538
c DMN017 Diamond-Blackfan Anemia 10 29 0.028
539
ATM016 Autoimmune Disease of Skin and Connective Tissue 29 0.028
540
c DMN018 Diamond-Blackfan Anemia 5 29 0.028
541
c PNC111 Pancreatic Cancer 2 28 0.028
542
PHG002 Phagocyte Bactericidal Dysfunction 28 0.028
543
IMM080 Immunodeficiency 23 27 0.028
544
IMM070 Immunodeficiency 13 27 0.028
545
c PNC094 Pancreatic Cancer 1 27 0.028
546
FNC005 Functional Colonic Disease 27 0.028
547
c DMN022 Diamond-Blackfan Anemia 9 26 0.028
548
IMM074 Immunodeficiency 16 26 0.028
549
c DMN020 Diamond-Blackfan Anemia 8 26 0.028
550
IMM075 Immunodeficiency 22 26 0.028
551
c WSK002 Wiskott-Aldrich Syndrome 2 25 0.028
552
c CNG022 Congenital Granular Cell Tumor 24 0.028
553
ACT234 Acute Myeloid Leukemia with Minimal Differentiation 22 0.028
554
c WLM005 Wilms Tumor 2 20 0.028
555
IMM142 Immunodeficiency 50 20 0.028
556
c WLM011 Wilms Tumor 6 19 0.028
557
VSC009 Vascular Skin Disease 19 0.028
558
AML051 Aml with Myelodysplasia-Related Features 18 0.028
559
CHR176 Chromophil Renal Cell Carcinoma 16 0.028
560
c LNG001 Lung Clear Cell Carcinoma 15 0.028
561
OVR020 Ovarian Wilms' Cancer 14 0.028
562
c SCN042 Secondary Hypereosinophilic Syndrome 14 0.028
563
LYM117 Lymphocytic Hypereosinophilic Syndrome 14 0.028
564
c FML303 Familial/multiple Cancer 14 0.028
565
SPL010 Splenic Manifestation of Hairy Cell Leukemia 12 0.028
566
CMP062 Complication After Organ Transplantation 11 0.028
567
P BRS047 Breast Cancer 100 0.023
568
P LNG032 Lung Cancer 95 0.023
569
P PRS040 Prostate Cancer 90 0.023
570
c SYS001 Systemic Lupus Erythematosus 86 0.023
571
HV1006 Hiv-1 80 0.023
572
P HNT016 Huntington Disease 80 0.023
573
P ATX030 Ataxia-Telangiectasia 77 0.023
574
P LVR013 Liver Disease 75 0.023
575
CRH001 Crohn's Disease 75 0.023
576
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.023
577
SQM006 Squamous Cell Carcinoma 70 0.023
578
THY028 Thyroid Cancer 69 0.023
579
P HPT021 Hepatitis 69 0.023
580
P MYP004 Myopathy 67 0.023
581
P NSP012 Nasopharyngeal Carcinoma 66 0.023
582
DWN001 Down Syndrome 66 0.023
583
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.023
584
CNT098 Central Core Disease 65 0.023
585
PTR006 Peters Anomaly 65 0.023
586
P PLR004 Pleuropulmonary Blastoma 65 0.023
587
c HPT016 Hepatitis B 64 0.023
588
P LPS004 Lupus Erythematosus 64 0.023
589
P ART023 Arthropathy 64 0.023
590
CHD001 Chediak-Higashi Syndrome 64 0.023
591
PSR001 Psoriatic Arthritis 64 0.023
592
P HYP086 Hypothyroidism 64 0.023
593
ALC007 Alcohol Dependence 63 0.023
594
P OST001 Osteopetrosis 63 0.023
595
P MDL022 Medullary Thyroid Carcinoma, Familial 63 0.023
596
P ADD001 Addison's Disease 62 0.023
597
P VLC001 Velocardiofacial Syndrome 62 0.023
598
APH001 Aphthous Stomatitis 62 0.023
599
P ALP009 Alopecia Areata 62 0.023
600
BRS051 Breast Disease 61 0.023
601
ACQ007 Acquired Immunodeficiency Syndrome 60 0.023
602
P GLM045 Glioma 60 0.023
603
QFV001 Q Fever 60 0.023
604
P SPN052 Spondyloarthropathy 60 0.023
605
WLL001 Williams-Beuren Syndrome 60 0.023
606
SPT004 Septic Arthritis 60 0.023
607
CRV038 Cervical Squamous Cell Carcinoma 60 0.023
608
GLB001 Gilbert Syndrome 60 0.023
609
LPD008 Lipid Metabolism Disorder 58 0.023
610
P GT001 Gout 58 0.023
611
P CTR002 Cataract 58 0.023
612
ADN018 Adenoma 58 0.023
613
RHM027 Rheumatic Disease 58 0.023
614
P BRS044 Breast Adenocarcinoma 58 0.023
615
P MSC007 Muscle Hypertrophy 58 0.023
616
SYN007 Synovitis 58 0.023
617
P LRY044 Larynx Cancer 57 0.023
618
CTS003 Coats Disease 57 0.023
619
EMB004 Embryonal Carcinoma 57 0.023
620
FCT006 Factor V Deficiency 57 0.023
621
P EXN002 Exanthem 57 0.023
622
ALP008 Alopecia 57 0.023
623
ORL015 Oral Squamous Cell Carcinoma 57 0.023
624
c ACT210 Acute Respiratory Distress Syndrome 57 0.023
625
EXF001 Exfoliation Syndrome 57 0.023
626
SVR066 Severe Combined Immunodeficiency, X-Linked 57 0.023
627
HYP266 Hypoxia 56 0.023
628
PHR003 Pharyngitis 56 0.023
629
P PLY019 Polyneuropathy 56 0.023
630
GST023 Gastric Ulcer 56 0.023
631
P HMR012 Hemorrhagic Fever 56 0.023
632
JNT002 Joint Disorders 55 0.023
633
P TMT001 Timothy Syndrome 55 0.023
634
MLN007 Male Infertility 55 0.023
635
MCS002 Mucositis 55 0.023
636
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.023
637
THL016 Thalassemias, Alpha- 53 0.023
638
SLP005 Sleep Disorder 53 0.023
639
P FBR031 Febrile Seizures 53 0.023
640
P LPC002 Lip Cancer 53 0.023
641
P ATX004 Ataxia 53 0.023
642
P DGR001 Digeorge Syndrome 53 0.023
643
P CYS018 Cystitis 52 0.023
644
BLM002 Bulimia Nervosa 52 0.023
645
PRT058 Pure Autonomic Failure 52 0.023
646
ALL026 Allergic Hypersensitivity Disease 52 0.023
647
P MSC033 Muscle Disorders 52 0.023
648
OPT006 Optic Nerve Disease 52 0.023
649
MST016 Mesothelioma, Somatic 51 0.023
650
SPN051 Spondylitis 51 0.023
651
CLN019 Colonic Disease 51 0.023
652
BRS099 Breast Ductal Carcinoma 50 0.023
653
P CHR345 Chronic Pain 50 0.023
654
c ACT068 Acute Cystitis 50 0.023
655
URN009 Urinary System Disease 50 0.023
656
P CLL015 Collagen Disease 50 0.023
657
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.023
658
c MLG079 Malignant Pleural Mesothelioma 50 0.023
659
c ACT134 Acute Liver Failure 50 0.023
660
P URF003 Urofacial Syndrome 1 50 0.023
661
END035 Endocrine Gland Cancer 49 0.023
662
P INT063 Intellectual Disability 49 0.023
663
c DWL002 Dowling-Degos Disease 1 49 0.023
664
c RTN162 Retinitis Pigmentosa 2 48 0.023
665
MSS002 Mass Syndrome 48 0.023
666
THY030 Thyroid Gland Disease 48 0.023
667
P TRC086 Trichohepatoenteric Syndrome 1 48 0.023
668
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 47 0.023
669
LPM005 Lipomatosis 47 0.023
670
THY009 Thyroid Lymphoma 47 0.023
671
AMN002 Amino Acid Metabolic Disorder 47 0.023
672
c INT072 Intestinal Pseudo-Obstruction 46 0.023
673
HMN032 Human Herpesvirus 8 46 0.023
674
LBL001 Lobular Neoplasia 46 0.023
675
SML036 Small Intestinal Adenocarcinoma 46 0.023
676
RLP003 Relapsing Fever 45 0.023
677
RNL078 Renal Dysplasia 45 0.023
678
P PLN008 Peeling Skin Syndrome 45 0.023
679
CLL002 Collecting Duct Carcinoma 45 0.023
680
HDN002 Head Injury 45 0.023
681
c CLR085 Colorectal Cancer 1 45 0.023
682
ORP003 Oropharynx Cancer 45 0.023
683
THR042 Thrombocytopenia, X-Linked 45 0.023
684
MNC006 Monoclonal Gammopathy of Uncertain Significance 44 0.023
685
TNS004 Tonsil Cancer 44 0.023
686
c MTR002 Mitral Valve Insufficiency 44 0.023
687
BNN003 Bone Inflammation Disease 44 0.023
688
PHR002 Pharyngoconjunctival Fever 44 0.023
689
P PHR004 Pharynx Cancer 44 0.023
690
PLR006 Pleural Cancer 44 0.023
691
P DMY001 Demyelinating Polyneuropathy 43 0.023
692
P PRL003 Proliferative Glomerulonephritis 43 0.023
693
EXC002 Exocrine Pancreatic Insufficiency 43 0.023
694
HYP082 Hypopharynx Cancer 43 0.023
695
c ART120 Arthrogryposis, Distal, Type 3 42 0.023
696
SPN119 Spondylarthropathy 42 0.023
697
PRT026 Parotitis 42 0.023
698
P PNC045 Pancreatic Agenesis 42 0.023
699
HPT020 Hepatic Vascular Disease 42 0.023
700
PLM039 Pulmonary Neuroendocrine Tumor 42 0.023
701
IND002 Indolent Systemic Mastocytosis 41 0.023
702
c CTR115 Cataract 16, Multiple Types 41 0.023
703
OPP002 Opportunistic Mycosis 41 0.023
704
BLS007 Blastic Plasmacytoid Dendritic Cell 41 0.023
705
END038 Endocrine Pancreas Disease 41 0.023
706
P BNG032 Benign Mesothelioma 40 0.023
707
MTR008 Mature B-Cell Neoplasm 40 0.023
708
c PLN018 Peeling Skin Syndrome 2 40 0.023
709
LNG030 Lung Adenoma 40 0.023
710
SPN369 Spinal Disease 39 0.023
711
APP010 Appendix Cancer 39 0.023
712
c CTR103 Cataract 4, Multiple Types 39 0.023
713
THL010 Thalassemia Minor 39 0.023
714
PGM003 Pigmentation Disease 39 0.023
715
PDT001 Pediatric Lymphoma 38 0.023
716
P LNG035 Lung Large Cell Carcinoma 38 0.023
717
SPC003 Specific Developmental Disorder 38 0.023
718
P OCY001 Oocyte Maturation Defect 38 0.023
719
c CNG031 Congenital Nervous System Abnormality 37 0.023
720
c CTR141 Cataract 21, Multiple Types 37 0.023
721
c CTR098 Cataract 1, Multiple Types 37 0.023
722
CNG069 Congenital Cytomegalovirus 36 0.023
723
c INH004 Inherited Blood Coagulation Disease 36 0.023
724
P WGN003 Wagner Syndrome 36 0.023
725
IMM065 Immunodeficiency 10 36 0.023
726
RDT001 Radiation Cystitis 36 0.023
727
CHP002 Chops Syndrome 35 0.023
728
ATM012 Autoimmune Disease of Blood 35 0.023
729
c CHR087 Chronic Cystitis 35 0.023
730
NNF001 Non-Functioning Pancreatic Endocrine Tumor 35 0.023
731
GST015 Gastric Small Cell Carcinoma 35 0.023
732
NNT007 Neonatal Leukemia 35 0.023
733
CLN005 Colon Lymphoma 35 0.023
734
WST003 West Nile Fever 34 0.023
735
c PLN017 Peeling Skin Syndrome 1 34 0.023
736
MSC004 Muscle Tissue Disease 34 0.023
737
GLS018 Glass Syndrome 34 0.023
738
LRY017 Laryngeal Disease 34 0.023
739
MXD032 Mixed Germ Cell Tumor 34 0.023
740
c CTR095 Cataract 8, Multiple Types 34 0.023
741
ACT177 Acute Basophilic Leukemia 34 0.023
742
NNT011 Neonatal Anemia 33 0.023
743
LNS003 Lens Disease 33 0.023
744
TXC007 Toxic Pneumonitis 33 0.023
745
c CTR132 Cataract 3, Multiple Types 33 0.023
746
HMR023 Hemorrhagic Cystitis 33 0.023
747
c SYS043 Systemic Lupus Erythematosus 1 33 0.023
748
MLG012 Malignant Epithelial Mesothelioma 33 0.023
749
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.023
750
FNC006 Functional Gastric Disease 32 0.023
751
c CTR124 Cataract 10, Multiple Types 32 0.023
752
c CTR122 Cataract 5, Multiple Types 32 0.023
753
PNT001 Pontiac Fever 32 0.023
754
LNG054 Lung Agenesis 32 0.023
755
c CTR102 Cataract 2, Multiple Types 32 0.023
756
c CTR113 Cataract 11, Multiple Types 31 0.023
757
CVT001 Cavitary Optic Disc Anomalies 31 0.023
758
FST001 Foster-Kennedy Syndrome 31 0.023
759
FNC012 Functioning Pancreatic Endocrine Tumor 31 0.023
760
P HYP078 Hypertrophy of Breast 31 0.023
761
MXD025 Mixed Germ Cell Cancer 31 0.023
762
SPC006 Specific Granule Deficiency 30 0.023
763
c CLR087 Colorectal Cancer 12 30 0.023
764
P SCK034 Sickle Beta Thalassemia 30 0.023
765
PLT019 Platelet Disorder, Familial, with Associated Myeloid Malignancy 30 0.023
766
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.023
767
CYL001 Cayler Cardiofacial Syndrome 29 0.023
768
c DRR009 Diarrhea 6 29 0.023
769
GRN016 Grant Syndrome 29 0.023
770
c PNC103 Pancreatic Cancer 4 29 0.023
771
IMM099 Immunodeficiency 33 29 0.023
772
IMM081 Immunodeficiency 19 29 0.023
773
c CLR079 Colorectal Cancer 2 29 0.023
774
c CLR075 Colorectal Cancer 3 28 0.023
775
TMR001 Tumor of Exocrine Pancreas 28 0.023
776
c WGN005 Wagner Syndrome 1 28 0.023
777
GLC043 Glucocorticoid Deficiency 2 28 0.023
778
NTR036 Neutropenia, Severe Congenital, X-Linked 28 0.023
779
c FBR072 Febrile Seizures, Familial, 11 27 0.023
780
c SYS038 Systemic Lupus Erythematosus 2 27 0.023
781
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.023
782
c CTR134 Cataract 23 27 0.023
783
c CTR127 Cataract 19 27 0.023
784
IMM036 Immunodeficiency, Isolated 27 0.023
785
LRG016 Large Intestine Adenocarcinoma 26 0.023
786
c CTR131 Cataract 17, Multiple Types 26 0.023
787
NTR042 Neutrophilic Dermatosis, Acute Febrile 25 0.023
788
c INH015 Inherited Acute Myeloid Leukemia 25 0.023
789
OVR069 Ovarian Germ Cell Tumor 24 0.023
790
c CTR116 Cataract 15, Multiple Types 24 0.023
791
ERY051 Erythroleukemia, Familial 23 0.023
792
GRW032 Growth Factors, Combined Defect of 22 0.023
793
c CLR081 Colorectal Cancer 6 22 0.023
794
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 22 0.023
795
DFF009 Diffuse Lipomatosis 21 0.023
796
c PNC105 Pancreatic Agenesis 2 21 0.023
797
TST035 Testicular Anomalies with or Without Congenital Heart Disease 21 0.023
798
c SYS046 Systemic Lupus Erythematosus 3 21 0.023
799
c NSP014 Nasopharyngeal Carcinoma, 3 21 0.023
800
c DMN030 Diamond-Blackfan Anemia 13 20 0.023
801
CHR208 Chromosome 17p Deletion 20 0.023
802
c SYS051 Systemic Lupus Erythematosus 4 20 0.023
803
c SYS055 Systemic Lupus Erythematosus 12 20 0.023
804
DFF010 Diffuse Alopecia Areata 20 0.023
805
CLN008 Colon Small Cell Carcinoma 19 0.023
806
c SYS053 Systemic Lupus Erythematosus 5 18 0.023
807
c CTR157 Cataract 28 18 0.023
808
SPC022 Specific Antibody Deficiency 18 0.023
809
c CTR161 Cataract 19 Multiple Types 18 0.023
810
INF009 Inflammatory Spondylopathy 18 0.023
811
c SPN226 Spondyloarthropathy 2 18 0.023
812
c ALP039 Alopecia Areata 1 18 0.023
813
FML125 Familial Hodgkin Disease 17 0.023
814
PNC007 Pancreas Lymphoma 17 0.023
815
c TCL008 T-Cell Lymphoma 1a 17 0.023
816
BNP001 Bone Peripheral Neuroepithelioma 17 0.023
817
c SYS048 Systemic Lupus Erythematosus 8 16 0.023
818
ISL032 Isolated Bone Marrow Mastocytosis 16 0.023
819
FRB003 Fairbank Disease 16 0.023
820
APP002 Appendix Lymphoma 15 0.023
821
LPN002 Lip and Oral Cavity Cancer 15 0.023
822
c ALP040 Alopecia Areata 2 15 0.023
823
PPL010 Papillary Follicular Thyroid Adenocarcinoma 14 0.023
824
P SKN009 Skin Granular Cell Tumor 14 0.023
825
c NTR008 Neutropenia Chronic Familial 14 0.023
826
UPP009 Upper Limb Hypertrophy 14 0.023
827
c DGR004 Digeorge Syndrome 2 14 0.023
828
THR106 Therapy Related Acute Myeloid Leukemia and Myelodysplastic Syndrome 14 0.023
829
PNC051 Pancreatic Cancer, Childhood 13 0.023
830
HVS002 Hiv-Associated Cancer 13 0.023
831
CHR561 Chromosome Breakage Syndromes 13 0.023
832
INB001 Inborn Amino Acid Metabolism Disorder 12 0.023
833
ADS006 Aids - Neurological Complications 12 0.023
834
c VLC003 Velocardiofacial Syndrome 2 12 0.023
835
P SYS050 Systemic Lupus Erythematosus with Nephritis 2 12 0.023
836
ORP004 Oropharyngeal Cancer, Adult 12 0.023
837
c SYS056 Systemic Lupus Erythematosus with Nephritis 1 12 0.023
838
c SYS054 Systemic Lupus Erythematosus with Nephritis 3 12 0.023
839
ORL014 Oral Pharyngeal Disorders 11 0.023
840
EXT049 Extramedullary Soft Tissue Plasmacytoma 11 0.023
841
IMM004 Immunoglobulin Beta Deficiency 11 0.023
842
c HRD112 Hereditary Thrombocytopenia with Normal Platelets 10 0.023
843
PRT056 Protein R Deficiency 10 0.023
844
CRC007 Carcinoid Tumor Childhood 8 0.023
845
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.016
846
P PLM037 Pulmonary Hypertension 79 0.016
847
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.016
848
ESP021 Esophageal Cancer 76 0.016
849
END057 Endometrial Cancer 75 0.016
850
STR067 Stroke, Ischemic 75 0.016
851
P LFR001 Li-Fraumeni Syndrome 75 0.016
852
P PFF001 Pfeiffer Syndrome 73 0.016
853
c HPT073 Hepatitis C Virus 73 0.016
854
CNG034 Congestive Heart Failure 72 0.016
855
ADR007 Adrenoleukodystrophy 72 0.016
856
P PLM036 Pulmonary Fibrosis 71 0.016
857
c ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.016
858
P RSP003 Respiratory Failure 71 0.016
859
P NRB001 Neuroblastoma 70 0.016
860
BRN028 Brain Cancer 70 0.016
861
TBR010 Tuberculosis 70 0.016
862
P MTC003 Metachromatic Leukodystrophy 70 0.016
863
c MLT136 Multiple Endocrine Neoplasia 1 69 0.016
864
P KRB001 Krabbe Disease 69 0.016
865
c HPT001 Hepatitis C 68 0.016
866
CMM004 Common Variable Immunodeficiency 68 0.016
867
P GLB002 Glioblastoma 68 0.016
868
P CRD011 Cardiomyopathy 68 0.016
869
WRN001 Werner Syndrome 67 0.016
870
PLM001 Pulmonary Tuberculosis 67 0.016
871
VSC007 Vascular Disease 67 0.016
872
OMN001 Omenn Syndrome 67 0.016
873
P CHR071 Charcot-Marie-Tooth Disease 67 0.016
874
P KDN018 Kidney Disease 66 0.016
875
URN008 Urinary Bladder Cancer 66 0.016
876
SRC014 Sarcoma 66 0.016
877
CRV047 Cervical Cancer, Somatic 65 0.016
878
P TRN020 Turner Syndrome 65 0.016
879
P NMN002 Niemann-Pick Disease 65 0.016
880
c BSL007 Basal Cell Carcinoma 65 0.016
881
P HRP006 Herpes Simplex 65 0.016
882
P AST007 Astrocytoma 65 0.016
883
P AGM001 Agammaglobulinemia 64 0.016
884
c MLT024 Multiple Endocrine Neoplasia Iia 64 0.016
885
c MCP037 Mucopolysaccharidosis is 64 0.016
886
P PRM019 Premature Ovarian Failure 64 0.016
887
LNG099 Lung Disease 64 0.016
888
P OST002 Osteoporosis 64 0.016
889
P INF037 Inflammatory Bowel Disease 63 0.016
890
P ALX003 Alexander Disease 63 0.016
891
GLN010 Glanzmann Thrombasthenia 63 0.016
892
OST085 Osteosarcoma, Somatic 63 0.016
893
WGN006 Wegener Granulomatosis 63 0.016
894
GLB015 Glioblastoma Multiforme 63 0.016
895
P RFS001 Refsum Disease 63 0.016
896
P MCL013 Mucolipidosis Iv 62 0.016
897
P CRN015 Cornelia De Lange Syndrome 62 0.016
898
VSC011 Vasculitis 62 0.016
899
P GCH001 Gaucher's Disease 62 0.016
900
GLC037 Glucocorticoid Resistance 62 0.016
901
ACN011 Acne 62 0.016
902
c MCP009 Mucopolysaccharidosis Ii 62 0.016
903
c MCP003 Mucopolysaccharidosis Vii 62 0.016
904
FCT007 Factor Vii Deficiency 61 0.016
905
TKY002 Takayasu Arteritis 61 0.016
906
MTH009 Mouth Disease 61 0.016
907
P RCK004 Rickets 61 0.016
908
MSL001 Measles 61 0.016
909
P PNC044 Pancreatitis 61 0.016
910
P SYS005 Systemic Scleroderma 61 0.016
911
c LCL006 Localized Scleroderma 61 0.016
912
P MCP010 Mucopolysaccharidosis 60 0.016
913
P FCL005 Focal Segmental Glomerulosclerosis 60 0.016
914
P INT068 Intestinal Disease 60 0.016
915
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.016
916
c VRL010 Viral Hepatitis 60 0.016
917
P CLR108 Colorectal Adenoma 60 0.016
918
MLG108 Malignant Melanoma, Somatic 60 0.016
919
c MCP024 Mucopolysaccharidosis Type Vi 60 0.016
920
c MCP004 Mucopolysaccharidosis Iv 60 0.016
921
P UVL004 Uveal Melanoma 60 0.016
922
c HPT003 Hepatitis a 59 0.016
923
GST045 Gastroenteritis 59 0.016
924
P ENC018 Encephalopathy 59 0.016
925
INT066 Interstitial Lung Disease 59 0.016
926
P NRP001 Neuropathy 59 0.016
927
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.016
928
P LKD001 Leukodystrophy 59 0.016
929
PGT001 Paget's Disease of Bone 59 0.016
930
c MCP001 Mucopolysaccharidosis Iii 58 0.016
931
RSP006 Respiratory System Disease 58 0.016
932
P MCR010 Microcephaly 58 0.016
933
ARM001 Aromatase Deficiency 58 0.016
934
P CMR001 Camurati-Engelmann Disease 58 0.016
935
P MTR004 Maturity-Onset Diabetes of the Young 58 0.016
936
MLG056 Malignant Hyperthermia 58 0.016
937
LYM021 Lymphadenitis 58 0.016
938
P HST010 Histiocytosis 58 0.016
939
P PNL012 Penile Cancer 58 0.016
940
RHB003 Rhabdomyosarcoma 57 0.016
941
ART017 Aortic Disease 57 0.016
942
P FCS002 Fucosidosis 57 0.016
943
ADR005 Adrenal Carcinoma 57 0.016
944
ADM013 Adamantinoma of Long Bones 57 0.016
945
SFT003 Soft Tissue Sarcoma 57 0.016
946
THR024 Thrombosis 57 0.016
947
PNC033 Pancreas Adenocarcinoma 57 0.016
948
P AGM005 Agammaglobulinemia, X-Linked 1 57 0.016
949
c SVR001 Severe Acute Respiratory Syndrome 57 0.016
950
SNS001 Sensorineural Hearing Loss 57 0.016
951
EPD016 Epidermolysis Bullosa 57 0.016
952
P INT070 Intestinal Obstruction 57 0.016
953
NRM005 Neuromuscular Disease 56 0.016
954
END041 Endometrial Adenocarcinoma 56 0.016
955
ZLL001 Zellweger Syndrome 56 0.016
956
P MLT074 Multiple Endocrine Neoplasia 56 0.016
957
P WVR001 Weaver Syndrome 56 0.016
958
LTT002 Letterer-Siwe Disease 56 0.016
959
PRS047 Prostatitis 56 0.016
960
P ANT006 Antiphospholipid Syndrome 56 0.016
961
GST050 Gastrointestinal System Disease 56 0.016
962
c MNN025 Mannosidosis, Alpha-, Types I and Ii 55 0.016
963
GRY002 Gray Platelet Syndrome 55 0.016
964
LKC001 Leukocyte Adhesion Deficiency 55 0.016
965
ASP002 Aspartylglucosaminuria 55 0.016
966
HPT022 Hepatoblastoma 55 0.016
967
PPL022 Papilloma 55 0.016
968
P EPD009 Epidermolysis Bullosa Dystrophica 54 0.016
969
c THR092 Thrombophilia Due to Thrombin Defect 54 0.016
970
P EMB005 Embryonal Rhabdomyosarcoma 54 0.016
971
c PND001 Pain Disorder 54 0.016
972
CHN016 Cohen Syndrome 54 0.016
973
LNG039 Lung Squamous Cell Carcinoma 54 0.016
974
P MCR129 Microvascular Complications of Diabetes 1 54 0.016
975
IMM111 Immunodeficiency, X-Linked, with Hyper-Igm 54 0.016
976
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.016
977
MCN017 Meconium Ileus 54 0.016
978
ESP023 Esophageal Disease 54 0.016
979
PLN006 Poland Syndrome 54 0.016
980
CND002 Conduct Disorder 54 0.016
981
CRV040 Cervix Carcinoma 53 0.016
982
P MTC069 Mitochondrial Disorders 53 0.016
983
DMY004 Demyelinating Disease 53 0.016
984
GST027 Gastric Lymphoma 53 0.016
985
LGS001 Legius Syndrome 53 0.016
986
TRN018 Transitional Cell Carcinoma 53 0.016
987
P HYP024 Hypoparathyroidism 53 0.016
988
WHM001 Whim Syndrome 53 0.016
989
BLT006 Bilateral Breast Cancer 53 0.016
990
LYS002 Lysosomal Storage Disease 52 0.016
991
BRN106 Burns 52 0.016
992
KRT002 Keratomalacia 52 0.016
993
BLR006 Biliary Tract Disease 52 0.016
994
OST015 Osteochondrodysplasia 52 0.016
995
c HPT015 Hepatitis D 52 0.016
996
c INF023 Inflammatory Breast Carcinoma 52 0.016
997
GST040 Gastric Adenocarcinoma 52 0.016
998
PRT011 Protein C Deficiency 52 0.016
999
c PRX045 Peroxisome Biogenesis Disorder 1b 52 0.016
1000
MYC002 Mycobacterium Avium Complex Disease 52 0.016
1001
PRS042 Prostate Disease 52 0.016
1002
IRN001 Iron Deficiency Anemia 52 0.016
1003
ATY005 Atypical Teratoid Rhabdoid Tumor 52 0.016
1004
NRP015 Neuropathy, Congenital Hypomyelinating 52 0.016
1005
BLD044 Bladder Disease 51 0.016
1006
PHL006 Phelan-Mcdermid Syndrome 51 0.016
1007
BRN038 Bronchial Disease 51 0.016
1008
c INF071 Inflammatory Bowel Disease 1 51 0.016
1009
TXC002 Toxic Encephalopathy 51 0.016
1010
P ESN008 Eosinophilic Pneumonia 51 0.016
1011
ADN009 Adenosquamous Carcinoma 51 0.016
1012
P GND004 Gonadal Dysgenesis 51 0.016
1013
P GRS003 Griscelli Syndrome 51 0.016
1014
CLR109 Colorectal Adenocarcinoma 51 0.016
1015
c MLT086 Multiple Endocrine Neoplasia, Type Iv 51 0.016
1016
SPN041 Spinal Cord Disease 51 0.016
1017
DSS009 Disseminated Intravascular Coagulation 51 0.016
1018
c GRS014 Griscelli Syndrome, Type 2 51 0.016
1019
BLD131 Bladder Urothelial Carcinoma 51 0.016
1020
PLG002 Plague 51 0.016
1021
c MLG068 Malignant Glioma 51 0.016
1022
RTC002 Reticular Dysgenesis 50 0.016
1023
INT007 Intermediate Coronary Syndrome 50 0.016
1024
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 50 0.016
1025
CLN015 Colon Adenocarcinoma 50 0.016
1026
THY025 Thymus Cancer 50 0.016
1027
HPT046 Hepatic Veno-Occlusive Disease 50 0.016
1028
RTN023 Retinitis 50 0.016
1029
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 50 0.016
1030
DBF001 D-Bifunctional Protein Deficiency 50 0.016
1031
RSS002 Roussy-Levy Syndrome 50 0.016
1032
STM007 Stomatitis 50 0.016
1033
PRR016 Pierre Robin Syndrome 50 0.016
1034
RHB001 Rhabdoid Cancer 50 0.016
1035
DRG003 Drug Dependence 50 0.016
1036
c MLG054 Malignant Histiocytosis 49 0.016
1037
ERY017 Erythema Elevatum Diutinum 49 0.016
1038
LPD009 Lipid Storage Disease 49 0.016
1039
UTR033 Uterine Corpus Cancer 49 0.016
1040
GLM004 Gliomatosis Cerebri 49 0.016
1041
PRN021 Paranasal Sinus Disease 49 0.016
1042
c INF067 Inflammatory Bowel Disease 10 49 0.016
1043
BLR007 Biliary Tract Neoplasm 49 0.016
1044
MLL012 Miller Syndrome 49 0.016
1045
c CNG464 Congenital Myopathy 49 0.016
1046
ACT017 Acute Chest Syndrome 48 0.016
1047
ADR012 Adrenal Gland Disease 48 0.016
1048
c ATS275 Autosomal Recessive Primary Microcephaly 48 0.016
1049
MYL003 Myeloid Sarcoma 48 0.016
1050
CRN017 Coronary Thrombosis 48 0.016
1051
P EST001 Estrogen-Receptor Positive Breast Cancer 48 0.016
1052
RHB009 Rhabdomyosarcoma 2, Alveolar 48 0.016
1053
BRN032 Brain Glioma 48 0.016
1054
P CTN003 Cutaneous Lupus Erythematosus 48 0.016
1055
c HMG001 Hemoglobin C Disease 47 0.016
1056
CYT005 Cytomegalovirus Retinitis 47 0.016
1057
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.016
1058
P VGN017 Vaginal Cancer 47 0.016
1059
PRT030 Parathyroid Gland Disease 47 0.016
1060
NNT017 Neonatal Adrenoleukodystrophy 47 0.016
1061
IMM104 Immunodeficiency with Hyper-Igm, Type 2 47 0.016
1062
c GRS013 Griscelli Syndrome, Type 1 47 0.016
1063
SYN036 Syncope 47 0.016
1064
DSM007 Desmoplastic Small Round Cell Tumor 47 0.016
1065
DWR001 Dwarfism 47 0.016
1066
NLS001 Nelson Syndrome 47 0.016
1067
P MNN018 Mannosidosis 47 0.016
1068
HMS001 Hemosiderosis 46 0.016
1069
LMT001 Limited Scleroderma 46 0.016
1070
CRB025 Carbohydrate Metabolic Disorder 46 0.016
1071
c GMM003 Gamma Heavy Chain Disease 46 0.016
1072
PRS039 Prostate Adenocarcinoma 46 0.016
1073
c CLR017 Clear Cell Sarcoma 46 0.016
1074
ANL017 Anal Squamous Cell Carcinoma 46 0.016
1075
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.016
1076
GLT021 Glutaricaciduria, Type I 46 0.016
1077
EMB007 Embryonal Sarcoma 46 0.016
1078
SKL014 Skeletal Dysplasia 46 0.016
1079
VCC001 Vaccinia 46 0.016
1080
INT067 Interstitial Nephritis 46 0.016
1081
P HRD021 Hereditary Sensory Neuropathy 46 0.016
1082
CD4003 Cd40 Ligand Deficiency 46 0.016
1083
BRL007 Bare Lymphocyte Syndrome, Type Ii, Complementation Group C 46 0.016
1084
P ACT150 Acute Adrenal Insufficiency 45 0.016
1085
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.016
1086
SNS003 Sensory Peripheral Neuropathy 45 0.016
1087
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 45 0.016
1088
P PLM025 Pulmonary Venoocclusive Disease 45 0.016
1089
IMM105 Immunodeficiency with Hyper-Igm, Type 3 45 0.016
1090
ATN004 Autonomic Neuropathy 45 0.016
1091
FBR086 Fibrolamellar Carcinoma 45 0.016
1092
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 45 0.016
1093
CCN007 Cocoon Syndrome 45 0.016
1094
SPH010 Sphingolipidosis 45 0.016
1095
SKL017 Skeletal Dysplasias 45 0.016
1096
ACH037 Achalasia-Addisonianism-Alacrimia Syndrome 45 0.016
1097
DYS164 Dyskeratosis Congenita, X-Linked 44 0.016
1098
VLV032 Vulva Cancer 44 0.016
1099
BND015 Band-Like Calcification with Simplified Gyration and Polymicrogyria 44 0.016
1100
CHR276 Chronic Active Epstein-Barr Virus Infection 44 0.016
1101
P BRN120 Bronchus Cancer 44 0.016
1102
BWN001 Bowen-Conradi Syndrome 44 0.016
1103
SRC027 Sarcoma, Synovial 44 0.016
1104
c HMG003 Hemoglobin E Disease 44 0.016
1105
NCR004 Nocardiosis 43 0.016
1106
PHY002 Physical Disorder 43 0.016
1107
BNW001 Bone Ewing's Sarcoma 43 0.016
1108
EPT010 Epithelial-Myoepithelial Carcinoma 43 0.016
1109
RNL097 Renal Artery Disease 43