Search results for Clofarabine

273 hits were found for Clofarabine

# Family MCID Name MIFTS Score
1
P LKM002 Leukemia 66 0.657
2
c LKM061 Leukemia, Acute Myeloid 83 0.614
3
P MYL006 Myeloid Leukemia 60 0.585
4
P LYM031 Lymphocytic Leukemia 55 0.547
5
P LKM062 Leukemia, Acute Lymphoblastic 68 0.523
6
MYL009 Myelodysplastic Syndrome 70 0.465
7
c CHR064 Chronic Monocytic Leukemia 34 0.434
8
c ACT073 Acute Leukemia 58 0.433
9
P LYM118 Lymphoma 68 0.419
10
LYM019 Lymphosarcoma 47 0.410
11
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.405
12
LYM040 Lymphoblastic Lymphoma 54 0.364
13
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.349
14
P GRF003 Graft-Versus-Host Disease 71 0.300
15
ADL002 Adult Syndrome 69 0.264
16
HMT002 Hematologic Cancer 62 0.244
17
LYM133 Lymphoma, Hodgkin, Classic 69 0.238
18
DWN001 Down Syndrome 70 0.235
19
P NTR004 Neutropenia 63 0.229
20
c LKM071 Leukemia, Chronic Lymphocytic 79 0.212
21
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.209
22
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.198
23
c LKM063 Leukemia, Chronic Myeloid 71 0.194
24
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.194
25
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.194
26
P CNR004 Cone-Rod Dystrophy 2 71 0.179
27
MGK001 Megakaryocytic Leukemia 64 0.179
28
P CHR285 Chronic Myelomonocytic Leukemia 59 0.179
29
P TRN020 Turner Syndrome 65 0.175
30
c ACT135 Acute Graft Versus Host Disease 51 0.175
31
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.175
32
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.170
33
ERY051 Erythroleukemia, Familial 56 0.170
34
c LKM070 Leukemia, Acute Monocytic 53 0.170
35
MYL069 Myeloma, Multiple 85 0.166
36
ATX019 Ataxia with Vitamin E Deficiency 48 0.166
37
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.166
38
c CHR418 Chronic Leukemia 50 0.162
39
HML018 Homologous Wasting Disease 22 0.162
40
P BCL017 B-Cell Lymphoma 58 0.157
41
PLS009 Plasma Cell Neoplasm 51 0.157
42
c CHR417 Chronic Graft Versus Host Disease 56 0.152
43
ACT200 Acute Monoblastic Leukemia 55 0.152
44
P MNC007 Monocytic Leukemia 54 0.152
45
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.152
46
ACT098 Acute Erythroid Leukemia 48 0.152
47
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.152
48
c ADL093 Adult Acute Monocytic Leukemia 20 0.152
49
DFC004 Deficiency Anemia 75 0.137
50
MYL031 Myeloproliferative Neoplasm 65 0.137
51
49X006 49, Xxxxy Syndrome 41 0.137
52
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.137
53
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.132
54
BNM001 Bone Marrow Cancer 43 0.132
55
ACT119 Acute Promyelocytic Leukemia 63 0.126
56
MCS002 Mucositis 55 0.126
57
P HST010 Histiocytosis 53 0.126
58
BRK010 Burkitt Lymphoma 67 0.121
59
MNT001 Mantle Cell Lymphoma 66 0.121
60
LNG108 Langerhans Cell Histiocytosis 58 0.121
61
ACT177 Acute Basophilic Leukemia 34 0.121
62
P SRC025 Sarcoidosis 1 70 0.114
63
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.114
64
HDG004 Hodgkin's Granuloma 26 0.114
65
HDG006 Hodgkin's Paragranuloma 24 0.114
66
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.108
67
MYL005 Myelofibrosis 67 0.101
68
P FLL037 Follicular Lymphoma 66 0.101
69
ALL026 Allergic Hypersensitivity Disease 64 0.101
70
c ADL017 Adult T-Cell Leukemia 57 0.101
71
CPL003 Capillary Leak Syndrome 55 0.101
72
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.101
73
P TCL004 T-Cell Leukemia 47 0.101
74
c CHR682 Chronic Bilirubin Encephalopathy 38 0.101
75
P APL001 Aplastic Anemia 74 0.093
76
c RHB024 Rhabdomyosarcoma 2 65 0.093
77
BLR008 Bilirubin Metabolic Disorder 57 0.093
78
P EXN002 Exanthem 57 0.093
79
DFF005 Diffuse Large B-Cell Lymphoma 56 0.093
80
HYP005 Hypokalemia 55 0.093
81
PNC001 Pancytopenia 54 0.093
83
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.093
84
c FLL041 Follicular Lymphoma 1 49 0.093
85
RFR010 Refractory Anemia 48 0.093
86
48X005 48,xyyy 39 0.093
87
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.093
88
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.093
89
ACT118 Acute Non Lymphoblastic Leukemia 27 0.093
90
FCT007 Factor Vii Deficiency 66 0.085
91
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.085
92
c ACT020 Acute T Cell Leukemia 53 0.085
93
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.085
94
CHL061 Childhood Leukemia 50 0.085
95
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.085
96
47X002 47,xyy 49 0.085
97
PRL017 Prolymphocytic Leukemia 47 0.085
98
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.085
99
LTT002 Letterer-Siwe Disease 34 0.085
100
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.085
101
BND002 B- and T-Cell Mixed Leukemia 18 0.085
102
P THR014 Thrombocytopenia 68 0.076
103
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.076
104
P LYM033 Lymphoproliferative Syndrome 60 0.076
105
HPT046 Hepatic Veno-Occlusive Disease 56 0.076
106
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.076
107
MRG003 Marginal Zone B-Cell Lymphoma 53 0.076
108
SPL004 Splenic Marginal Zone Lymphoma 51 0.076
109
PLS025 Plasmablastic Lymphoma 47 0.076
110
P BNG032 Benign Mesothelioma 45 0.076
111
CYT002 Cytokine Deficiency 44 0.076
112
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.076
113
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.076
114
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.066
115
ADR007 Adrenoleukodystrophy 74 0.066
116
HMN044 Human Immunodeficiency Virus Type 1 71 0.066
117
P MTC003 Metachromatic Leukodystrophy 70 0.066
118
P KRB001 Krabbe Disease 69 0.066
119
P TYS001 Tay-Sachs Disease 68 0.066
120
SND001 Sandhoff Disease 68 0.066
121
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.066
122
MYC006 Mycosis Fungoides 66 0.066
123
SRC014 Sarcoma 65 0.066
124
c MCP001 Mucopolysaccharidosis Iii 65 0.066
125
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.066
126
LYS012 Lysosomal Acid Lipase Deficiency 64 0.066
127
c GM1007 Gm1 Gangliosidosis 61 0.066
128
P ANP001 Anaplastic Large Cell Lymphoma 61 0.066
129
LYM012 Lymphoplasmacytic Lymphoma 61 0.066
130
SZR001 Sezary's Disease 60 0.066
131
ACQ007 Acquired Immunodeficiency Syndrome 60 0.066
132
P LKD001 Leukodystrophy 59 0.066
133
c MST023 Mesothelioma, Malignant 57 0.066
134
SPN041 Spinal Cord Disease 56 0.066
135
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.066
136
PRP036 Peripheral T-Cell Lymphoma 53 0.066
137
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.066
138
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.066
139
SPN035 Spindle Cell Sarcoma 51 0.066
140
MCR004 Macroglobulinemia 50 0.066
141
c MLG054 Malignant Histiocytosis 50 0.066
142
RTC005 Reticulosarcoma 49 0.066
143
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.066
144
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.066
145
P MCL001 Mucolipidosis 47 0.066
146
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.066
147
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.066
148
PRX001 Peroxisomal Disease 46 0.066
149
c INH020 Inherited Metabolic Disorder 46 0.066
150
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.066
151
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.066
152
LYM051 Lymphomatoid Granulomatosis 45 0.066
153
MRG013 Mirage Syndrome 44 0.066
154
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.066
155
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.066
156
INT253 Intestinal Benign Neoplasm 44 0.066
157
P GNG009 Gangliosidosis 44 0.066
158
LTH001 Lethal Midline Granuloma 43 0.066
159
TST015 Testicular Disease 43 0.066
160
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.066
161
c PRM038 Primary Agammaglobulinemia 43 0.066
162
P 8P1002 8p11 Myeloproliferative Syndrome 39 0.066
163
c PNT037 Pontocerebellar Hypoplasia, Type 3 39 0.066
164
ADR022 Adrenomyeloneuropathy 38 0.066
165
INC022 Inclusion-Cell Disease 35 0.066
166
SML008 Small Intestine Lymphoma 35 0.066
167
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.066
168
PDT001 Pediatric Lymphoma 33 0.066
169
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 28 0.066
170
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.066
171
CHL079 Children's Interstitial Lung Disease 27 0.066
173
P RFR014 Refractory Anemia with Excess Blasts Type 2 18 0.066
174
P BRS047 Breast Cancer 96 0.054
175
c FNC027 Fanconi Anemia, Complementation Group a 81 0.054
176
SCK003 Sickle Cell Anemia 72 0.054
177
PRP027 Peripheral Vascular Disease 71 0.054
178
P NRB001 Neuroblastoma 71 0.054
179
P OST001 Osteopetrosis 71 0.054
180
P KDN018 Kidney Disease 70 0.054
181
c WLM013 Wilms Tumor 1 65 0.054
182
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.054
183
c MCL013 Mucolipidosis Iv 64 0.054
184
P VSC007 Vascular Disease 63 0.054
185
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.054
186
P RHB003 Rhabdomyosarcoma 62 0.054
187
c WLM018 Wilms Tumor 5 62 0.054
188
c ALP101 Alpha-Thalassemia 62 0.054
189
P TST021 Testicular Germ Cell Tumor 61 0.054
190
OST003 Osteonecrosis 61 0.054
191
P PNC044 Pancreatitis 61 0.054
192
P THL005 Thalassemia 60 0.054
193
c ACT071 Acute Kidney Failure 59 0.054
194
P SZR006 Seizure Disorder 58 0.054
195
P PRP019 Peripheral Nervous System Disease 57 0.054
196
P NRP001 Neuropathy 56 0.054
197
c GM1004 Gm1-Gangliosidosis, Type I 56 0.054
198
PGM001 Pigmented Villonodular Synovitis 56 0.054
199
SFT003 Soft Tissue Sarcoma 56 0.054
200
BCT022 Bacterial Infectious Disease 56 0.054
201
CMR002 Coumarin Resistance 56 0.054
202
HMG005 Hemoglobinopathy 55 0.054
203
HRY003 Hairy Cell Leukemia 55 0.054
204
c OST131 Osteopetrosis, Autosomal Dominant 2 54 0.054
205
c MCP043 Mucopolysaccharidosis, Type Iiia 54 0.054
206
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.054
207
LYS002 Lysosomal Storage Disease 52 0.054
208
P FNC004 Fanconi Syndrome 50 0.054
209
P SCK005 Sickle Cell Disease 50 0.054
210
RSD004 Rosai-Dorfman Disease 50 0.054
211
MYL003 Myeloid Sarcoma 49 0.054
212
CHR563 Chronic Eosinophilic Leukemia 48 0.054
213
CNG028 Congenital Hypoplastic Anemia 46 0.054
214
GLY031 Glycoproteinosis 46 0.054
215
PLS016 Plasma Cell Leukemia 46 0.054
216
c SPR009 Sporadic Breast Cancer 45 0.054
217
P TST026 Testicular Germ Cell Cancer 44 0.054
218
c JVN003 Juvenile Xanthogranuloma 44 0.054
219
OVR112 Ovarian Germ Cell Cancer 43 0.054
220
TRP009 Triple X Syndrome 42 0.054
221
CHR286 Chronic Neutrophilic Leukemia 41 0.054
222
SPR126 Superior Semicircular Canal Dehiscence 40 0.054
223
c MLG074 Malignant Mesenchymoma 39 0.054
224
OVR094 Ovarian Epithelial Cancer 38 0.054
225
c HMG029 Hemoglobin Se Disease 38 0.054
226
c WLM011 Wilms Tumor 6 37 0.054
227
GRM010 Germ Cells Tumors 34 0.054
228
RFR002 Refractory Hairy Cell Leukemia 32 0.054
229
MCL022 Mucolipidoses 30 0.054
230
c TST046 Testicular Germ Cell Tumor 1 29 0.054
231
CLS052 Classic Hairy Cell Leukemia 27 0.054
232
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 26 0.054
233
TST003 Testicular Leukemia 26 0.054
234
MLG164 Malignant Epithelial Tumor of Ovary 26 0.054
235
P HPT023 Hepatocellular Carcinoma 100 0.038
236
P CLR023 Colorectal Cancer 98 0.038
237
c SYS001 Systemic Lupus Erythematosus 86 0.038
238
P PNC035 Pancreatic Cancer 84 0.038
239
P BLD134 Bladder Cancer 78 0.038
240
P HRT032 Heart Disease 75 0.038
241
GLB015 Glioblastoma Multiforme 75 0.038
242
P RSP003 Respiratory Failure 74 0.038
243
CRH001 Crohn's Disease 74 0.038
244
P FML011 Familial Adenomatous Polyposis 72 0.038
245
MLN008 Melanoma 69 0.038
246
EWN003 Ewing Sarcoma 68 0.038
247
c INF071 Inflammatory Bowel Disease 1 68 0.038
248
SKN019 Skin Melanoma 67 0.038
249
P VSC011 Vasculitis 62 0.038
250
TXC005 Toxic Shock Syndrome 61 0.038
251
TKY002 Takayasu Arteritis 61 0.038
252
P ENC018 Encephalopathy 61 0.038
253
P LPS004 Lupus Erythematosus 61 0.038
254
ATM095 Autoimmune Disease 61 0.038
255
P BNG030 Benign Ependymoma 60 0.038
256
PRT058 Pure Autonomic Failure 59 0.038
257
P CYS018 Cystitis 59 0.038
258
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.038
259
TRN018 Transitional Cell Carcinoma 56 0.038
260
CLL010 Cellular Ependymoma 53 0.038
261
CRH005 Crohn's Colitis 52 0.038
262
P CTN015 Cutaneous T Cell Lymphoma 49 0.038
263
GYN001 Gynecomastia 49 0.038
264
BCT021 Bacterial Sepsis 44 0.038
265
c ADL052 Adult Acute Lymphocytic Leukemia 40 0.038
266
HMR023 Hemorrhagic Cystitis 38 0.038
267
c SYS043 Systemic Lupus Erythematosus 1 38 0.038
268
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 38 0.038
269
ATM052 Autoimmune Disease 1 37 0.038
270
ATY022 Atypical Coarctation of Aorta 35 0.038
271
PDT014 Pediatric Ependymoma 32 0.038
272
INF021 Infant Gynecomastia 31 0.038
273
c DRR018 Diarrhea 9 29 0.038
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