Search results for Busulfan

655 hits were found for Busulfan

# Family MCID Name MIFTS Score
1
P GRF003 Graft-Versus-Host Disease 72 0.590
2
P LKM002 Leukemia 68 0.555
3
P MYL006 Myeloid Leukemia 60 0.549
4
c LKM061 Leukemia, Acute Myeloid 84 0.514
5
MYL009 Myelodysplastic Syndrome 70 0.474
6
P LYM118 Lymphoma 68 0.421
7
LYM019 Lymphosarcoma 46 0.406
8
c LKM063 Leukemia, Chronic Myeloid 72 0.404
9
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.376
10
c ACT135 Acute Graft Versus Host Disease 52 0.375
11
HPT046 Hepatic Veno-Occlusive Disease 56 0.360
12
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.360
13
P LKM062 Leukemia, Acute Lymphoblastic 69 0.350
14
MYL069 Myeloma, Multiple 85 0.349
15
LYM133 Lymphoma, Hodgkin, Classic 69 0.345
16
c CHR064 Chronic Monocytic Leukemia 33 0.325
17
c ACT073 Acute Leukemia 58 0.312
18
PLS009 Plasma Cell Neoplasm 51 0.310
19
c CHR417 Chronic Graft Versus Host Disease 57 0.308
20
HMT002 Hematologic Cancer 62 0.305
21
LYM040 Lymphoblastic Lymphoma 54 0.287
22
HML018 Homologous Wasting Disease 22 0.287
23
DFC004 Deficiency Anemia 70 0.279
24
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.277
25
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.272
26
P CNR004 Cone-Rod Dystrophy 2 73 0.270
27
MCS002 Mucositis 56 0.270
28
P LKM071 Leukemia, Chronic Lymphocytic 79 0.255
29
P BCL017 B-Cell Lymphoma 58 0.252
30
MYL031 Myeloproliferative Neoplasm 66 0.251
31
ADL002 Adult Syndrome 70 0.247
32
BNM001 Bone Marrow Cancer 43 0.238
33
P CHR285 Chronic Myelomonocytic Leukemia 60 0.234
34
MYL005 Myelofibrosis 70 0.226
35
RFR010 Refractory Anemia 48 0.224
36
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.223
37
P FLL037 Follicular Lymphoma 67 0.215
38
MNT001 Mantle Cell Lymphoma 69 0.213
39
c FLL041 Follicular Lymphoma 1 49 0.210
40
BRK010 Burkitt Lymphoma 67 0.203
41
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.201
42
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.200
43
PLS025 Plasmablastic Lymphoma 47 0.200
44
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.200
45
P TRN020 Turner Syndrome 67 0.196
46
CHL149 Childhood Acute Myeloid Leukemia 44 0.194
47
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.191
48
P NRB001 Neuroblastoma 72 0.189
49
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.189
50
IMM167 Immune Deficiency Disease 78 0.187
51
MRG003 Marginal Zone B-Cell Lymphoma 52 0.181
52
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.181
53
SPL004 Splenic Marginal Zone Lymphoma 51 0.173
54
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.173
55
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.171
56
P PLY018 Polycythemia 56 0.169
57
P APL001 Aplastic Anemia 74 0.167
58
PLY001 Polycythemia Vera 69 0.167
59
ATY042 Atypical Chronic Myeloid Leukemia 49 0.165
60
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.165
61
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.165
62
P SZR006 Seizure Disorder 56 0.161
63
DFF005 Diffuse Large B-Cell Lymphoma 55 0.161
64
SVR004 Severe Combined Immunodeficiency 73 0.159
65
c PRM038 Primary Agammaglobulinemia 44 0.159
67
P CYS018 Cystitis 59 0.154
68
P THL005 Thalassemia 60 0.152
69
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.150
70
P ESS003 Essential Thrombocythemia 68 0.147
71
HMR023 Hemorrhagic Cystitis 45 0.147
72
MGK001 Megakaryocytic Leukemia 64 0.145
73
48X005 48,xyyy 39 0.145
74
c RHB024 Rhabdomyosarcoma 2 67 0.142
75
WLD007 Waldenstroem's Macroglobulinemia 61 0.142
76
ERY051 Erythroleukemia, Familial 56 0.142
77
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.142
78
MCR004 Macroglobulinemia 49 0.142
79
RTC005 Reticulosarcoma 47 0.142
80
P NTR004 Neutropenia 63 0.137
81
VSL002 Visual Epilepsy 59 0.137
82
EWN003 Ewing Sarcoma 69 0.135
83
c PRM012 Primary Polycythemia 50 0.135
84
CMB003 Combined T Cell and B Cell Immunodeficiency 49 0.135
85
CMB081 Combined Immunodeficiency, X-Linked 36 0.135
86
c LKM070 Leukemia, Acute Monocytic 57 0.132
87
HMG005 Hemoglobinopathy 56 0.132
88
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.132
89
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.132
90
c LKM005 Leukemia, T-Cell, Chronic 34 0.132
91
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.130
92
P LYM033 Lymphoproliferative Syndrome 59 0.130
93
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.130
94
LYM012 Lymphoplasmacytic Lymphoma 47 0.130
95
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.130
96
SRC014 Sarcoma 65 0.127
97
P ADL017 Adult T-Cell Leukemia 56 0.127
98
c THR090 Thrombocythemia 1 49 0.127
99
LYM051 Lymphomatoid Granulomatosis 45 0.127
100
c FNC027 Fanconi Anemia, Complementation Group a 81 0.124
101
P SRC025 Sarcoidosis 1 70 0.124
102
SFT003 Soft Tissue Sarcoma 56 0.124
103
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.124
104
FNG017 Fungal Infectious Disease 53 0.124
105
SPN035 Spindle Cell Sarcoma 53 0.124
106
c CHR418 Chronic Leukemia 49 0.124
107
CHR286 Chronic Neutrophilic Leukemia 42 0.124
108
P MLG074 Malignant Mesenchymoma 40 0.124
109
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.124
110
HDG004 Hodgkin's Granuloma 23 0.124
111
HDG006 Hodgkin's Paragranuloma 22 0.124
112
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.121
113
MYC006 Mycosis Fungoides 66 0.121
114
SZR001 Sezary's Disease 60 0.121
115
STM007 Stomatitis 50 0.121
116
P SCK005 Sickle Cell Disease 50 0.121
117
CHR563 Chronic Eosinophilic Leukemia 48 0.121
118
ACT098 Acute Erythroid Leukemia 48 0.121
119
P CHR012 Chronic Granulomatous Disease 67 0.118
120
P CNT005 Central Nervous System Lymphoma 53 0.118
121
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.118
122
P MDL005 Medulloblastoma 77 0.115
123
SCK003 Sickle Cell Anemia 74 0.115
124
P MNC007 Monocytic Leukemia 53 0.115
125
ACT200 Acute Monoblastic Leukemia 52 0.115
126
c BTT014 Beta-Thalassemia 74 0.112
127
P RHB003 Rhabdomyosarcoma 63 0.112
128
P ANP001 Anaplastic Large Cell Lymphoma 58 0.112
129
c PRM226 Primary Central Nervous System Lymphoma 48 0.112
130
c CHR682 Chronic Bilirubin Encephalopathy 39 0.112
131
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.112
132
c ADL093 Adult Acute Monocytic Leukemia 20 0.112
133
PLS011 Plasmacytoma 56 0.109
134
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.109
135
P THR014 Thrombocytopenia 67 0.106
136
PNC001 Pancytopenia 54 0.106
137
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.106
138
P FNC004 Fanconi Syndrome 50 0.106
139
LTH001 Lethal Midline Granuloma 44 0.106
140
P CTN015 Cutaneous T Cell Lymphoma 49 0.102
141
ACT119 Acute Promyelocytic Leukemia 63 0.099
142
c ALP101 Alpha-Thalassemia 62 0.099
143
VRL011 Viral Infectious Disease 61 0.099
144
AZS001 Azoospermia 50 0.099
145
PRL017 Prolymphocytic Leukemia 47 0.099
146
SPR126 Superior Semicircular Canal Dehiscence 40 0.099
147
c HMG029 Hemoglobin Se Disease 39 0.099
148
P PLM036 Pulmonary Fibrosis 65 0.095
149
HRY003 Hairy Cell Leukemia 55 0.095
150
P DMN001 Diamond-Blackfan Anemia 69 0.092
151
P MLN007 Male Infertility 55 0.092
152
CYS036 Cystinosis, Nephropathic 51 0.092
153
CNT033 Central Nervous System Cancer 47 0.092
154
P FNC034 Fanconi Renotubular Syndrome 2 40 0.092
155
HMN044 Human Immunodeficiency Virus Type 1 71 0.088
156
P HPT021 Hepatitis 67 0.088
157
FCT007 Factor Vii Deficiency 67 0.088
158
NTR005 Nutritional Deficiency Disease 62 0.088
159
ACQ007 Acquired Immunodeficiency Syndrome 60 0.088
160
P EXN002 Exanthem 57 0.088
161
INT054 Intraocular Lymphoma 48 0.088
162
c INH020 Inherited Metabolic Disorder 47 0.088
163
P GLM040 Glioma Susceptibility 1 81 0.084
164
DWN001 Down Syndrome 70 0.084
165
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.084
166
P CTR002 Cataract 60 0.084
167
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.084
168
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.084
169
P ALP008 Alopecia 54 0.084
170
PLS016 Plasma Cell Leukemia 53 0.084
171
PRP036 Peripheral T-Cell Lymphoma 53 0.084
172
HST010 Histiocytosis 48 0.084
173
SPL018 Splenomegaly 48 0.084
174
RFR002 Refractory Hairy Cell Leukemia 33 0.084
175
CLS052 Classic Hairy Cell Leukemia 27 0.084
176
P LNG032 Lung Cancer 98 0.079
177
P WSK001 Wiskott-Aldrich Syndrome 72 0.079
178
c WLM013 Wilms Tumor 1 65 0.079
179
P GLM045 Glioma 63 0.079
180
c WLM018 Wilms Tumor 5 61 0.079
181
P BNG030 Benign Ependymoma 60 0.079
182
LNG108 Langerhans Cell Histiocytosis 58 0.079
183
CLL010 Cellular Ependymoma 54 0.079
184
HMS001 Hemosiderosis 54 0.079
185
c DMN023 Diamond-Blackfan Anemia 1 53 0.079
186
GLL048 Glial Tumor 45 0.079
187
P RRH023 Rare Hereditary Hemochromatosis 41 0.079
188
c WLM011 Wilms Tumor 6 37 0.079
189
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.079
190
P BRS047 Breast Cancer 97 0.075
191
ADR007 Adrenoleukodystrophy 75 0.075
192
P RSP003 Respiratory Failure 74 0.075
193
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.075
194
P LVR013 Liver Disease 68 0.075
195
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.075
196
P INF032 Infertility 57 0.075
197
P DRR001 Diarrhea 55 0.075
198
P AST007 Astrocytoma 51 0.075
199
GRM005 Germ Cell Cancer 47 0.075
200
c MLG068 Malignant Glioma 46 0.075
201
MXD026 Mixed Glioma 45 0.075
202
P EPN001 Ependymoblastoma 44 0.075
203
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.075
204
MXD050 Mixed Phenotype Acute Leukemia 43 0.075
205
CYT002 Cytokine Deficiency 42 0.075
206
CHL079 Children's Interstitial Lung Disease 26 0.075
207
SCH036 Scheie Syndrome 72 0.070
208
P KDN018 Kidney Disease 72 0.070
209
P AMY004 Amyloidosis 70 0.070
210
P OST001 Osteopetrosis 70 0.070
211
CMM004 Common Variable Immunodeficiency 68 0.070
212
P HYP098 Hypereosinophilic Syndrome 67 0.070
213
P MNN013 Meningitis 66 0.070
214
HRL003 Hurler Syndrome 65 0.070
215
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.070
216
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.070
217
P LKD001 Leukodystrophy 59 0.070
218
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.070
219
THR004 Thrombocytosis 51 0.070
220
c ALM001 Al Amyloidosis 50 0.070
221
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.070
222
47X002 47,xyy 49 0.070
223
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.070
224
c DRR009 Diarrhea 6 46 0.070
225
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.070
226
IMM136 Immune System Disease 45 0.070
227
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.070
228
ATX019 Ataxia with Vitamin E Deficiency 42 0.070
229
ADR022 Adrenomyeloneuropathy 38 0.070
230
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.065
231
P RTN024 Retinoblastoma 73 0.065
232
P KRB001 Krabbe Disease 69 0.065
233
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.065
234
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.065
235
CHD001 Chediak-Higashi Syndrome 66 0.065
236
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 0.065
237
CHN016 Cohen Syndrome 63 0.065
238
c SVR003 Severe Congenital Neutropenia 59 0.065
239
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.065
240
CMR002 Coumarin Resistance 56 0.065
241
HRL004 Hurler-Scheie Syndrome 55 0.065
242
c FML008 Familial Retinoblastoma 53 0.065
243
c INF023 Inflammatory Breast Carcinoma 50 0.065
244
ADN001 Adenosine Deaminase Deficiency 47 0.065
245
SPH010 Sphingolipidosis 47 0.065
246
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.065
247
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.065
248
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.065
249
LRG008 Large Granular Lymphocyte Leukemia 41 0.065
250
GRM010 Germ Cells Tumors 34 0.065
251
BRN028 Brain Cancer 74 0.059
252
P MTC003 Metachromatic Leukodystrophy 70 0.059
253
CNG034 Congestive Heart Failure 69 0.059
254
P MLN008 Melanoma 69 0.059
255
P PNM007 Pneumonia 68 0.059
256
SKN019 Skin Melanoma 68 0.059
257
P OLG002 Oligodendroglioma 67 0.059
258
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.059
259
c SML038 Small Cell Cancer of the Lung 65 0.059
260
P HRP006 Herpes Simplex 65 0.059
261
P PSR002 Psoriasis 62 0.059
262
FCS002 Fucosidosis 61 0.059
263
IRN002 Iron Metabolism Disease 57 0.059
264
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.059
265
CYT008 Cytomegalovirus Infection 57 0.059
266
HPT022 Hepatoblastoma 56 0.059
267
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.059
268
AMN001 Amenorrhea 54 0.059
269
c OST131 Osteopetrosis, Autosomal Dominant 2 53 0.059
270
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.059
271
PST011 Pustulosis of Palm and Sole 52 0.059
272
P BRN035 Brain Stem Glioma 52 0.059
273
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 51 0.059
274
TST014 Testicular Cancer 46 0.059
275
CRB026 Cerebellar Astrocytoma 37 0.059
276
ACT177 Acute Basophilic Leukemia 34 0.059
277
LTT002 Letterer-Siwe Disease 33 0.059
278
ENG004 Engraftment Syndrome 30 0.059
279
ACT118 Acute Non Lymphoblastic Leukemia 26 0.059
280
P HPT023 Hepatocellular Carcinoma 100 0.053
281
P OVR042 Ovarian Cancer 88 0.053
282
P PNC035 Pancreatic Cancer 84 0.053
283
GLB015 Glioblastoma Multiforme 75 0.053
284
CRH001 Crohn's Disease 74 0.053
285
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.053
286
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.053
287
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.053
288
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.053
289
RHB001 Rhabdoid Cancer 63 0.053
290
IMM174 Immunodeficiency with Hyper-Igm, Type 1 63 0.053
291
c HPT001 Hepatitis C 62 0.053
292
ALL026 Allergic Hypersensitivity Disease 62 0.053
293
TXC005 Toxic Shock Syndrome 62 0.053
294
ASP002 Aspartylglucosaminuria 62 0.053
295
HYP066 Hyperglycemia 61 0.053
296
P KDN017 Kidney Cancer 60 0.053
297
P TST021 Testicular Germ Cell Tumor 60 0.053
298
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.053
299
c HPT016 Hepatitis B 59 0.053
300
BRN002 Bronchiolitis 59 0.053
301
BLR008 Bilirubin Metabolic Disorder 57 0.053
302
PGM001 Pigmented Villonodular Synovitis 56 0.053
303
ISL001 Islet Cell Tumor 56 0.053
304
P INF037 Inflammatory Bowel Disease 54 0.053
305
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 54 0.053
306
HMG002 Hemoglobinuria 50 0.053
307
P PNB001 Pineoblastoma 50 0.053
308
CHL018 Childhood Medulloblastoma 49 0.053
309
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.053
310
GNG008 Ganglioneuroblastoma 48 0.053
311
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.053
312
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.053
313
CD4003 Cd40 Ligand Deficiency 46 0.053
314
PRX001 Peroxisomal Disease 46 0.053
315
EXT010 Extramedullary Plasmacytoma 45 0.053
316
P TST026 Testicular Germ Cell Cancer 43 0.053
317
GST020 Gastric Antral Vascular Ectasia 41 0.053
318
49X006 49, Xxxxy Syndrome 41 0.053
319
c OVR114 Ovarian Cancer 1 38 0.053
320
MCP033 Mucopolysaccharidoses 38 0.053
321
CHL057 Childhood Brain Stem Glioma 32 0.053
322
PDT014 Pediatric Ependymoma 32 0.053
323
DFF031 Diffuse Alveolar Hemorrhage 30 0.053
324
c TST046 Testicular Germ Cell Tumor 1 29 0.053
325
HMP028 Hemophagocytic Syndrome Associated with an Infection 24 0.053
326
PDT016 Pediatric Infratentorial Ependymoma 22 0.053
328
P RFR014 Refractory Anemia with Excess Blasts Type 2 18 0.053
329
c RFR015 Refractory Anemia with Excess Blasts Type 1 15 0.053
330
CHL009 Childhood Cerebral Astrocytoma 14 0.053
331
P HRT032 Heart Disease 75 0.046
332
c MNN043 Meningioma, Familial 74 0.046
333
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.046
334
MST024 Mastocytosis, Cutaneous 69 0.046
335
P MYC084 Mycobacterium Tuberculosis 1 68 0.046
336
PCK003 Pick Disease of Brain 68 0.046
337
c NMN015 Niemann-Pick Disease, Type C1 68 0.046
338
P FRN006 Frontotemporal Dementia 68 0.046
339
P PLM037 Pulmonary Hypertension 67 0.046
340
OST159 Osteogenic Sarcoma 66 0.046
341
P SKN015 Skin Carcinoma 66 0.046
342
c MCL013 Mucolipidosis Iv 66 0.046
343
P ADL010 Adult Respiratory Distress Syndrome 65 0.046
344
P THY023 Thymoma 65 0.046
345
LYS012 Lysosomal Acid Lipase Deficiency 65 0.046
346
P ADN016 Adenocarcinoma 64 0.046
347
RBR001 Roberts Syndrome 64 0.046
348
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.046
349
SKN016 Skin Disease 63 0.046
350
ERL001 Early Myoclonic Encephalopathy 62 0.046
351
CLT003 Colitis 62 0.046
352
c NMN013 Niemann-Pick Disease, Type a 62 0.046
353
ATM095 Autoimmune Disease 62 0.046
354
MNN042 Meningioma, Radiation-Induced 62 0.046
355
CHL068 Cholestasis 61 0.046
356
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.046
357
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.046
358
P ALP009 Alopecia Areata 60 0.046
359
P NMN002 Niemann-Pick Disease 59 0.046
360
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.046
361
c NMN016 Niemann-Pick Disease, Type B 58 0.046
362
CRD132 Cardiac Conduction Defect 58 0.046
363
MCS006 Macs Syndrome 58 0.046
364
c DWL002 Dowling-Degos Disease 1 58 0.046
365
GLS018 Glass Syndrome 57 0.046
366
THY022 Thymic Carcinoma 57 0.046
367
AYM001 Ayme-Gripp Syndrome 57 0.046
368
BCT022 Bacterial Infectious Disease 56 0.046
369
BRN012 Bronchiolitis Obliterans 55 0.046
370
PRP030 Purpura 54 0.046
371
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.046
372
CLR030 Clear Cell Renal Cell Carcinoma 53 0.046
373
P EPD016 Epidermolysis Bullosa 53 0.046
374
TXC002 Toxic Encephalopathy 53 0.046
375
c PSR017 Psoriasis 2 53 0.046
376
LYS002 Lysosomal Storage Disease 52 0.046
377
c VRL010 Viral Hepatitis 52 0.046
378
c THY107 Thymoma, Familial 52 0.046
379
c PSR023 Psoriasis 1 52 0.046
380
c CNG208 Congenital Disorder of Glycosylation, Type Iic 51 0.046
381
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.046
382
SPN021 Spinal Meningioma 50 0.046
383
MYL003 Myeloid Sarcoma 49 0.046
384
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.046
385
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.046
386
c PSR032 Psoriasis 11 47 0.046
387
P CHR573 Choroid Plexus Cancer 46 0.046
388
TCL003 T Cell Deficiency 46 0.046
389
OLG001 Oligospermia 45 0.046
390
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.046
391
PNC056 Pineocytoma 45 0.046
393
ANP009 Anaplastic Oligodendroglioma 43 0.046
394
c PSR028 Psoriasis 7 42 0.046
395
P PRT026 Parotitis 42 0.046
396
IMM078 Immunodeficiency 21 42 0.046
397
PNL014 Pineal Gland Cancer 41 0.046
398
c PSR018 Psoriasis 13 41 0.046
399
SCR001 Secretory Meningioma 41 0.046
400
P 8P1002 8p11 Myeloproliferative Syndrome 39 0.046
401
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.046
402
THR123 Thrombotic Microangiopathy 36 0.046
403
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.046
404
CHR178 Chromosomal Triplication 35 0.046
405
P INH011 Inherited Bone Marrow Failure Syndromes 34 0.046
406
VRS001 Virus Associated Hemophagocytic Syndrome 32 0.046
407
ACD003 Acid Sphingomyelinase Deficiency 32 0.046
408
CHL006 Childhood Oligodendroglioma 31 0.046
409
RFR004 Refractory Hematologic Cancer 30 0.046
410
MYC088 Mycobacterium Avium Complex Infections 29 0.046
411
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 29 0.046
412
BRN049 Brain Tumor, Childhood 29 0.046
413
P CNT036 Central Nervous System Germ Cell Tumor 28 0.046
414
P SCK034 Sickle Beta Thalassemia 28 0.046
415
TST003 Testicular Leukemia 27 0.046
416
PGM030 Pigmentation Anomaly of the Skin 26 0.046
417
CHL015 Childhood Choroid Plexus Cancer 16 0.046
418
c SYS001 Systemic Lupus Erythematosus 86 0.037
419
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.037
420
BRT054 Brittle Bone Disorder 72 0.037
421
c HPT073 Hepatitis C Virus 72 0.037
422
AGM019 Agammaglobulinemia, X-Linked 71 0.037
423
PRP027 Peripheral Vascular Disease 71 0.037
424
c GCH015 Gaucher Disease, Type I 70 0.037
425
P TYS001 Tay-Sachs Disease 69 0.037
426
P SYS005 Systemic Scleroderma 68 0.037
427
SND001 Sandhoff Disease 68 0.037
428
BRN024 Bronchitis 68 0.037
429
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.037
430
P SHW006 Shwachman-Diamond Syndrome 1 67 0.037
431
P DMN002 Dementia 66 0.037
432
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.037
433
P DRM053 Dermatitis, Atopic 66 0.037
434
KHL003 Kohlschutter-Tonz Syndrome 65 0.037
435
P AGM001 Agammaglobulinemia 65 0.037
436
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.037
437
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.037
438
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.037
439
P MST009 Mastocytosis 64 0.037
440
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.037
441
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.037
442
RFS006 Refsum Disease, Classic 64 0.037
443
P GCH001 Gaucher's Disease 63 0.037
444
P HML002 Hemolytic Anemia 63 0.037
445
P VSC007 Vascular Disease 63 0.037
446
c GM1007 Gm1 Gangliosidosis 62 0.037
447
c BRN108 Branchiootic Syndrome 1 62 0.037
448
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.037
449
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.037
450
DRM006 Dermatitis 61 0.037
451
c SCL052 Scleroderma, Familial Progressive 61 0.037
452
P ENC018 Encephalopathy 61 0.037
453
P LPS004 Lupus Erythematosus 61 0.037
454
HRP004 Herpes Zoster 60 0.037
455
PNM010 Pneumothorax, Primary Spontaneous 60 0.037
456
LNG099 Lung Disease 60 0.037
457
SQM006 Squamous Cell Carcinoma 60 0.037
458
P MCR010 Microcephaly 59 0.037
459
GRD007 Grade Iii Astrocytoma 59 0.037
460
CHR072 Chordoma 58 0.037
461
THY025 Thymus Cancer 58 0.037
462
LYM027 Lymphopenia 58 0.037
463
MCR013 Microphthalmia 57 0.037
464
P ZLL001 Zellweger Syndrome 57 0.037
465
APH002 Aphasia 57 0.037
466
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 57 0.037
467
c GM1004 Gm1-Gangliosidosis, Type I 57 0.037
468
PNM008 Pneumothorax 56 0.037
469
P FBR017 Fibrosarcoma 56 0.037
470
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.037
471
SPN041 Spinal Cord Disease 56 0.037
472
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.037
474
P DBT005 Diabetes Insipidus 55 0.037
475
GLS001 Gliosarcoma 54 0.037
476
PPL022 Papilloma 54 0.037
477
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.037
478
PST046 Post-Transplant Lymphoproliferative Disease 53 0.037
479
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.037
480
P PLM006 Pulmonary Alveolar Proteinosis 53 0.037
481
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.037
482
ACR041 Acromelic Frontonasal Dysostosis 52 0.037
483
P OVR049 Ovarian Disease 52 0.037
484
DSM007 Desmoplastic Small Round Cell Tumor 52 0.037
485
NTR018 Neutrophilia, Hereditary 52 0.037
486
P TRT010 Teratoma 52 0.037
487
FCT001 Factor Viii Deficiency 51 0.037
488
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 51 0.037
489
GNT002 Giant Cell Glioblastoma 50 0.037
490
c INF145 Infantile Liver Failure Syndrome 1 50 0.037
491
MLL001 Molluscum Contagiosum 50 0.037
492
c THR071 Thrombocytopenia 1 50 0.037
493
CLR003 Clear Cell Adenocarcinoma 50 0.037
494
DYS073 Dysphagia 50 0.037
495
P MST002 Mast-Cell Leukemia 49 0.037
496
GST049 Gastrointestinal System Cancer 49 0.037
497
SCT005 Scott Syndrome 49 0.037
498
c TCL005 T-Cell Prolymphocytic Leukemia 49 0.037
499
P SDR003 Sideroblastic Anemia 49 0.037
500
CHL061 Childhood Leukemia 48 0.037
501
WTH001 Withdrawal Disorder 48 0.037
502
P PRR002 Pure Red-Cell Aplasia 47 0.037
503
TTR011 Tetraploidy 47 0.037
504
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 47 0.037
505
GST071 Gastrointestinal Carcinoma 47 0.037
506
NDL013 Nodular Regenerative Hyperplasia 47 0.037
507
SQM002 Squamous Cell Papilloma 46 0.037
508
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.037
509
GLY031 Glycoproteinosis 45 0.037
510
c ZLL011 Zellweger Spectrum Disorder 45 0.037
511
OVR112 Ovarian Germ Cell Cancer 45 0.037
512
MCR225 Macrophage Activation Syndrome 44 0.037
513
CRD043 Ceroid Storage Disease 44 0.037
514
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 44 0.037
515
P GNG009 Gangliosidosis 44 0.037
516
SPN040 Spinal Cancer 44 0.037
517
MRG013 Mirage Syndrome 43 0.037
518
c MLG081 Malignant Teratoma 43 0.037
519
RDC006 Red Cell Aplasia 43 0.037
520
CRB138 Core Binding Factor Acute Myeloid Leukemia 43 0.037
521
TRP009 Triple X Syndrome 42 0.037
522
P AVS003 Avascular Necrosis 42 0.037
523
c HYP829 Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive 42 0.037
524
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.037
525
CMP009 Complement Deficiency 41 0.037
526
DFF003 Diffuse Scleroderma 41 0.037
527
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 38 0.037
528
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.037
529
KDN002 Kidney Rhabdoid Cancer 38 0.037
530
CHL010 Childhood Kidney Cell Carcinoma 38 0.037
531
c SYS043 Systemic Lupus Erythematosus 1 38 0.037
532
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 38 0.037
533
OPT032 Optic Pathway Glioma 35 0.037
534
c ADL008 Adult Oligodendroglioma 34 0.037
535
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.037
536
EXT025 Extragonadal Germ Cell Cancer 32 0.037
537
MDS019 Mediastinal Malignant Lymphoma 30 0.037
538
MCL022 Mucolipidoses 30 0.037
539
INT082 Intraocular Retinoblastoma 30 0.037
540
CYT018 Cytochrome P450 2d6 Variant 27 0.037
541
ACT162 Acute Sensory Ataxic Neuropathy 26 0.037
542
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.037
543
HRP008 Herpes Simiae 25 0.037
544
EXT029 Extraocular Retinoblastoma 24 0.037
545
PDT015 Pediatric Supratentorial Ependymoma 24 0.037
546
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.037
547
CHR208 Chromosome 17p Deletion 23 0.037
548
DCK002 Dock8 Immunodeficiency Syndrome 19 0.037
549
NNN002 Noninvasive Malignant Thymoma 11 0.037
550
CRB054 Cerebellar Astrocytoma, Childhood 9 0.037
551
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.026
552
STR067 Stroke, Ischemic 81 0.026
553
P BLD134 Bladder Cancer 79 0.026
554
END057 Endometrial Cancer 74 0.026
555
P MLT020 Multiple Sclerosis 72 0.026
556
P EPL164 Epilepsy 71 0.026
557
P HYP086 Hypothyroidism 69 0.026
558
P MYS003 Myasthenia Gravis 68 0.026
559
P DYS007 Dyskeratosis Congenita 67 0.026
560
CRB039 Cerebrovascular Disease 67 0.026
561
c HMP029 Hemophilia a 67 0.026
562
P PRP003 Porphyria Cutanea Tarda 67 0.026
563
c PRM196 Premature Ovarian Failure 1 67 0.026
564
GLN010 Glanzmann Thrombasthenia 66 0.026
565
P NRV007 Nervous System Disease 66 0.026
566
TTN003 Tetanus 65 0.026
567
END041 Endometrial Adenocarcinoma 63 0.026
568
c FNC043 Fanconi Anemia, Complementation Group E 62 0.026
569
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.026
570
P PRP029 Porphyria 62 0.026
571
OST003 Osteonecrosis 61 0.026
572
DPH001 Diphtheria 60 0.026
573
CRD223 Cardiac Arrhythmia 60 0.026
574
c ACT071 Acute Kidney Failure 60 0.026
575
DYS164 Dyskeratosis Congenita, X-Linked 60 0.026
576
P BRN019 Bernard-Soulier Syndrome 60 0.026
577
P BND020 Bone Disease 59 0.026
578
PNM001 Pneumocystosis 59 0.026
579
P SLP005 Sleep Disorder 59 0.026
580
PLM033 Pulmonary Embolism 59 0.026
581
P BRS044 Breast Adenocarcinoma 59 0.026
582
P PLY006 Polydactyly 59 0.026
583
GLB001 Gilbert Syndrome 58 0.026
584
ISC004 Ischemia 58 0.026
585
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.026
586
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.026
587
DSS009 Disseminated Intravascular Coagulation 57 0.026
588
TRN018 Transitional Cell Carcinoma 56 0.026
589
AGN016 Aging 56 0.026
590
PTS001 Patau Syndrome 55 0.026
591
ACT058 Active Peptic Ulcer Disease 55 0.026
592
BRN014 Bronchopneumonia 54 0.026
593
PLM010 Pulmonary Edema 54 0.026
594
P LTR001 Lateral Sclerosis 54 0.026
595
P INS002 in Situ Carcinoma 53 0.026
596
P HYP083 Hypopituitarism 53 0.026
597
P HML001 Hemolytic-Uremic Syndrome 53 0.026
598
c CNT035 Central Nervous System Disease 52 0.026
599
HYP088 Hyper-Igd Syndrome 52 0.026
600
c VRL005 Viral Pneumonia 52 0.026
601
P HMP007 Hemophilia 51 0.026
602
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 51 0.026
603
LNG031 Lung Benign Neoplasm 51 0.026
604
P RNL007 Renal Tubular Acidosis 51 0.026
605
END086 End Stage Renal Disease 51 0.026
606
ACT017 Acute Chest Syndrome 51 0.026
607
c CNG027 Congenital Hemolytic Anemia 50 0.026
608
HYP080 Hypogonadism 50 0.026
609
c ACQ017 Acquired Von Willebrand Syndrome 49 0.026
610
SLD003 Sialadenitis 49 0.026
611
EPD006 Epidermolysis Bullosa Acquisita 49 0.026
612
MLR002 Miliary Tuberculosis 49 0.026
613
BNR002 Bone Resorption Disease 48 0.026
614
ASP007 Aspiration Pneumonia 48 0.026
615
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 48 0.026
616
P ERY008 Erythromelalgia 47 0.026
617
c PRM093 Premature Ovarian Failure 7 47 0.026
618
GST010 Gestational Trophoblastic Neoplasm 46 0.026
619
P MYC033 Myoclonus 46 0.026
620
ASP008 Aspiration Pneumonitis 45 0.026
621
SPS057 Spasticity 45 0.026
622
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.026
623
P HYP073 Hypersensitivity Reaction Type Iv Disease 44 0.026
624
BCT021 Bacterial Sepsis 44 0.026
625
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.026
626
TST015 Testicular Disease 43 0.026
627
SNL007 Senile Cataract 42 0.026
628
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.026
629
ARC002 Arachnoiditis 42 0.026
630
FSR001 Fusariosis 42 0.026
631
THR035 Thrombasthenia 40 0.026
632
DND018 Dendritic Cell Tumor 40 0.026
633
c HMG001 Hemoglobin C Disease 40 0.026
634
P SPR119 Spermatogenic Failure, X-Linked, 1 39 0.026
635
CRB001 Cerebral Lymphoma 39 0.026
636
BLS007 Blastic Plasmacytoid Dendritic Cell 38 0.026
637
OVR094 Ovarian Epithelial Cancer 38 0.026
638
TRP005 Trophoblastic Neoplasm 38 0.026
639
c SCN052 Secondary Adrenal Insufficiency 36 0.026
640
SPN354 Spinal Arachnoiditis 36 0.026
641
c PRM340 Primary Adrenal Insufficiency 36 0.026
642
P PLY188 Polyendocrinopathy 32 0.026
643
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.026
644
TXC007 Toxic Pneumonitis 29 0.026
645
c DRR018 Diarrhea 9 28 0.026
646
LPD001 Lipid Pneumonia 28 0.026
647
HYP855 Hyperpigmentation of the Skin 27 0.026
648
c ATS210 Autosomal Recessive Sideroblastic Anemia 26 0.026
649
DFF010 Diffuse Alopecia Areata 26 0.026
650
MLG164 Malignant Epithelial Tumor of Ovary 26 0.026
652
IND005 Indolent B Cell Lymphoma 20 0.026
653
c CNT108 Central Polydactyly 15 0.026
654
TCL006 T Cell Immunodeficiency Primary 11 0.026
655
HMT020 Hematopoietic Stem Cell Kinetics, Control of 8 0.026
Content
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