Search results for Cytarabine

646 hits were found for Cytarabine

# Family MCID Name MIFTS Score
1
c LKM061 Leukemia, Acute Myeloid 83 1.040
2
P MYL006 Myeloid Leukemia 60 1.022
3
P LKM002 Leukemia 66 0.934
4
c CHR064 Chronic Monocytic Leukemia 34 0.725
5
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.724
6
P LYM118 Lymphoma 68 0.627
7
LYM019 Lymphosarcoma 47 0.602
8
P LYM031 Lymphocytic Leukemia 55 0.589
9
P LKM062 Leukemia, Acute Lymphoblastic 68 0.546
10
MYL009 Myelodysplastic Syndrome 70 0.544
11
c ACT073 Acute Leukemia 58 0.445
12
LYM040 Lymphoblastic Lymphoma 54 0.444
13
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.413
14
ADL002 Adult Syndrome 69 0.383
15
LYM133 Lymphoma, Hodgkin, Classic 69 0.380
16
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.349
17
c LKM063 Leukemia, Chronic Myeloid 71 0.323
18
P NTR004 Neutropenia 63 0.320
19
DWN001 Down Syndrome 70 0.307
20
P BCL017 B-Cell Lymphoma 58 0.307
21
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.306
22
MNT001 Mantle Cell Lymphoma 66 0.296
23
MGK001 Megakaryocytic Leukemia 64 0.291
24
c LKM070 Leukemia, Acute Monocytic 53 0.291
25
ERY051 Erythroleukemia, Familial 56 0.290
26
c RHB024 Rhabdomyosarcoma 2 65 0.284
27
c PRM038 Primary Agammaglobulinemia 43 0.258
28
P TRN020 Turner Syndrome 65 0.251
29
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.247
30
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.245
31
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.236
32
P MNC007 Monocytic Leukemia 54 0.232
33
P GRF003 Graft-Versus-Host Disease 71 0.230
34
48X005 48,xyyy 39 0.230
35
MCS002 Mucositis 55 0.229
36
BRK010 Burkitt Lymphoma 67 0.227
37
ACT200 Acute Monoblastic Leukemia 55 0.225
38
RFR010 Refractory Anemia 48 0.224
39
ACT098 Acute Erythroid Leukemia 48 0.224
40
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.222
41
DFF005 Diffuse Large B-Cell Lymphoma 56 0.220
42
P CHR285 Chronic Myelomonocytic Leukemia 59 0.219
43
ACT119 Acute Promyelocytic Leukemia 63 0.217
44
c PRM226 Primary Central Nervous System Lymphoma 47 0.214
45
DFC004 Deficiency Anemia 75 0.210
46
P CNT005 Central Nervous System Lymphoma 53 0.210
47
PLS025 Plasmablastic Lymphoma 47 0.205
48
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.205
49
c ADL093 Adult Acute Monocytic Leukemia 20 0.205
50
c LKM071 Leukemia, Chronic Lymphocytic 79 0.202
51
HMT002 Hematologic Cancer 62 0.200
52
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.200
53
P FLL037 Follicular Lymphoma 66 0.194
54
MYL031 Myeloproliferative Neoplasm 65 0.194
55
RTC005 Reticulosarcoma 49 0.194
56
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.192
57
c FLL041 Follicular Lymphoma 1 49 0.190
58
MYL069 Myeloma, Multiple 85 0.183
59
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.179
60
BNM001 Bone Marrow Cancer 43 0.172
61
PLS009 Plasma Cell Neoplasm 51 0.168
62
P THR014 Thrombocytopenia 68 0.166
63
49X006 49, Xxxxy Syndrome 41 0.162
64
P TCL004 T-Cell Leukemia 47 0.159
65
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.159
66
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.155
67
P CNR004 Cone-Rod Dystrophy 2 71 0.152
68
P MNN013 Meningitis 65 0.152
69
c CHR418 Chronic Leukemia 50 0.152
70
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.152
71
P EXN002 Exanthem 57 0.145
72
c ADL017 Adult T-Cell Leukemia 57 0.145
73
FCT007 Factor Vii Deficiency 66 0.143
74
ACT177 Acute Basophilic Leukemia 34 0.143
75
HMN044 Human Immunodeficiency Virus Type 1 71 0.135
76
P SRC025 Sarcoidosis 1 70 0.135
77
c ACT135 Acute Graft Versus Host Disease 51 0.135
78
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.132
79
47X002 47,xyy 49 0.132
80
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.132
81
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.132
82
P ANP001 Anaplastic Large Cell Lymphoma 61 0.129
83
BLR008 Bilirubin Metabolic Disorder 57 0.129
84
MRG003 Marginal Zone B-Cell Lymphoma 53 0.129
85
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.129
86
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.129
87
HDG004 Hodgkin's Granuloma 26 0.129
88
HDG006 Hodgkin's Paragranuloma 24 0.129
89
ACQ007 Acquired Immunodeficiency Syndrome 60 0.126
90
P DRR001 Diarrhea 57 0.126
91
c ACT020 Acute T Cell Leukemia 53 0.126
92
SPL004 Splenic Marginal Zone Lymphoma 51 0.126
93
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.126
94
ALL026 Allergic Hypersensitivity Disease 64 0.123
95
CMR002 Coumarin Resistance 56 0.123
96
STM007 Stomatitis 49 0.123
97
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 26 0.123
98
HPT046 Hepatic Veno-Occlusive Disease 56 0.120
99
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.120
100
CRB138 Core Binding Factor Acute Myeloid Leukemia 43 0.120
101
HML018 Homologous Wasting Disease 22 0.120
102
ATX019 Ataxia with Vitamin E Deficiency 48 0.117
103
c CHR417 Chronic Graft Versus Host Disease 56 0.114
104
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.114
105
ARC002 Arachnoiditis 42 0.114
106
SPN354 Spinal Arachnoiditis 36 0.114
107
P HYP098 Hypereosinophilic Syndrome 66 0.111
108
ATY042 Atypical Chronic Myeloid Leukemia 49 0.111
109
CYT002 Cytokine Deficiency 44 0.111
110
MYL005 Myelofibrosis 67 0.108
111
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.108
112
SRC014 Sarcoma 65 0.108
113
PNC001 Pancytopenia 54 0.108
114
TST015 Testicular Disease 43 0.108
115
P CNJ013 Conjunctivitis 65 0.104
116
P NRP001 Neuropathy 56 0.104
117
SPN035 Spindle Cell Sarcoma 51 0.104
118
TRP009 Triple X Syndrome 42 0.104
119
BND002 B- and T-Cell Mixed Leukemia 18 0.104
120
LNG108 Langerhans Cell Histiocytosis 58 0.101
121
P ALP008 Alopecia 56 0.101
122
P HST010 Histiocytosis 53 0.101
123
MYL003 Myeloid Sarcoma 49 0.101
125
IMM167 Immune Deficiency Disease 78 0.097
126
SFT003 Soft Tissue Sarcoma 56 0.097
127
CHL061 Childhood Leukemia 50 0.097
128
c MLG074 Malignant Mesenchymoma 39 0.097
129
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.097
130
ACT118 Acute Non Lymphoblastic Leukemia 27 0.093
131
TCL018 T-Cell Childhood Acute Lymphocytic Leukemia 19 0.093
132
P BRS047 Breast Cancer 96 0.089
133
P PRP019 Peripheral Nervous System Disease 57 0.089
134
c CNT035 Central Nervous System Disease 54 0.089
135
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.089
136
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.089
137
c ADL052 Adult Acute Lymphocytic Leukemia 40 0.089
138
P RSP003 Respiratory Failure 74 0.085
139
P NRV007 Nervous System Disease 66 0.085
140
PRP036 Peripheral T-Cell Lymphoma 53 0.085
141
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.085
142
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.085
143
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.085
144
PRL017 Prolymphocytic Leukemia 47 0.085
145
P CLR023 Colorectal Cancer 98 0.081
146
P OVR042 Ovarian Cancer 89 0.081
147
HRP004 Herpes Zoster 60 0.081
148
HYP005 Hypokalemia 55 0.081
149
TXC002 Toxic Encephalopathy 52 0.081
150
RCH001 Richter's Syndrome 45 0.081
151
c PNT037 Pontocerebellar Hypoplasia, Type 3 39 0.081
153
P MDL005 Medulloblastoma 77 0.076
154
LYM012 Lymphoplasmacytic Lymphoma 61 0.076
155
ATM095 Autoimmune Disease 61 0.076
156
MCR004 Macroglobulinemia 50 0.076
157
INT054 Intraocular Lymphoma 48 0.076
158
P NRV006 Nervous System Cancer 48 0.076
159
GRN017 Granulocytopenia 44 0.076
160
P CRN035 Cranial Nerve Palsy 41 0.076
161
CNT018 Central Nervous System Leukemia 35 0.076
162
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.076
163
P LNG032 Lung Cancer 97 0.071
164
SVR004 Severe Combined Immunodeficiency 73 0.071
165
PLY001 Polycythemia Vera 69 0.071
166
P ENC004 Encephalitis 61 0.071
167
P PNC044 Pancreatitis 61 0.071
168
P PLY018 Polycythemia 55 0.071
169
PRC013 Pericarditis 54 0.071
170
c CNT033 Central Nervous System Cancer 46 0.071
171
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 46 0.071
172
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.071
173
LTT002 Letterer-Siwe Disease 34 0.071
174
TST003 Testicular Leukemia 26 0.071
175
P LNG064 Lung Cancer Susceptibility 3 77 0.066
176
c MNN043 Meningioma, Familial 74 0.066
177
P RTN024 Retinoblastoma 72 0.066
178
P MLT020 Multiple Sclerosis 72 0.066
179
MLN008 Melanoma 69 0.066
180
EWN003 Ewing Sarcoma 68 0.066
181
P ESS003 Essential Thrombocythemia 67 0.066
182
P DMN002 Dementia 67 0.066
183
KHL003 Kohlschutter-Tonz Syndrome 64 0.066
184
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.066
185
NTR005 Nutritional Deficiency Disease 61 0.066
186
P LYM033 Lymphoproliferative Syndrome 60 0.066
187
LYM027 Lymphopenia 57 0.066
188
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.066
189
HRY003 Hairy Cell Leukemia 55 0.066
190
PLM010 Pulmonary Edema 55 0.066
191
c FML008 Familial Retinoblastoma 53 0.066
192
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.066
193
c PRM012 Primary Polycythemia 52 0.066
194
P PRC012 Pericardial Effusion 51 0.066
195
ENT011 Enterocolitis 50 0.066
196
SPL018 Splenomegaly 48 0.066
197
HMP001 Hemopericardium 46 0.066
198
CDQ001 Cauda Equina Syndrome 39 0.066
199
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.066
200
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.060
201
P APL001 Aplastic Anemia 74 0.060
202
c ATR087 Atrial Standstill 1 74 0.060
203
BRN028 Brain Cancer 73 0.060
204
ACR006 Aceruloplasminemia 73 0.060
205
CNG034 Congestive Heart Failure 70 0.060
206
P PNM007 Pneumonia 68 0.060
207
KRT019 Keratitis, Hereditary 67 0.060
208
P HPT021 Hepatitis 67 0.060
209
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.060
210
P ASP006 Aspergillosis 66 0.060
211
c SML038 Small Cell Cancer of the Lung 65 0.060
212
P HRP006 Herpes Simplex 65 0.060
213
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.060
214
RHB001 Rhabdoid Cancer 63 0.060
215
P ADL010 Adult Respiratory Distress Syndrome 63 0.060
216
PPL049 Papillon-Lefevre Syndrome 63 0.060
217
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.060
218
P CYS018 Cystitis 59 0.060
219
DSS009 Disseminated Intravascular Coagulation 57 0.060
220
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.060
221
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.060
222
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.060
223
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.060
225
c THR090 Thrombocythemia 1 49 0.060
226
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.060
227
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.060
228
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.060
229
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.060
230
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.060
231
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.060
232
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.060
233
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.060
234
c CHR682 Chronic Bilirubin Encephalopathy 38 0.060
235
ATM052 Autoimmune Disease 1 37 0.060
236
CHR178 Chromosomal Triplication 35 0.060
237
RFR004 Refractory Hematologic Cancer 30 0.060
238
CLS052 Classic Hairy Cell Leukemia 27 0.060
239
CHL079 Children's Interstitial Lung Disease 27 0.060
240
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.060
241
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 22 0.060
242
P RFR014 Refractory Anemia with Excess Blasts Type 2 18 0.060
243
P ATX030 Ataxia-Telangiectasia 83 0.054
244
GLB015 Glioblastoma Multiforme 75 0.054
245
P NRB001 Neuroblastoma 71 0.054
246
P ART022 Arthritis 70 0.054
247
SKN019 Skin Melanoma 67 0.054
248
MYC006 Mycosis Fungoides 66 0.054
249
c MCL013 Mucolipidosis Iv 64 0.054
250
c WLM018 Wilms Tumor 5 62 0.054
251
HYP066 Hyperglycemia 61 0.054
252
P LPS004 Lupus Erythematosus 61 0.054
253
OST003 Osteonecrosis 61 0.054
254
SZR001 Sezary's Disease 60 0.054
255
c ACT071 Acute Kidney Failure 59 0.054
256
IRN002 Iron Metabolism Disease 57 0.054
257
PLS011 Plasmacytoma 56 0.054
258
PRP030 Purpura 55 0.054
259
GLS018 Glass Syndrome 53 0.054
260
NTR018 Neutrophilia, Hereditary 52 0.054
261
TLN003 Telangiectasis 51 0.054
262
THR004 Thrombocytosis 51 0.054
263
c MLG054 Malignant Histiocytosis 50 0.054
264
PLS016 Plasma Cell Leukemia 46 0.054
265
LYM051 Lymphomatoid Granulomatosis 45 0.054
266
CHR286 Chronic Neutrophilic Leukemia 41 0.054
267
THR123 Thrombotic Microangiopathy 38 0.054
268
CRB001 Cerebral Lymphoma 38 0.054
269
c ATS384 Autosomal Dominant Non-Syndromic Intellectual Disability 2 31 0.054
270
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.054
271
LVR006 Liver Lymphoma 29 0.054
272
CYT018 Cytochrome P450 2d6 Variant 27 0.054
273
P HPT023 Hepatocellular Carcinoma 100 0.047
274
P PRS040 Prostate Cancer 97 0.047
275
c SYS001 Systemic Lupus Erythematosus 86 0.047
276
c TBR025 Tuberous Sclerosis 1 76 0.047
277
P HRT032 Heart Disease 75 0.047
278
SCK003 Sickle Cell Anemia 72 0.047
279
c TBR026 Tuberous Sclerosis 2 71 0.047
280
c HPT073 Hepatitis C Virus 70 0.047
281
P TBR001 Tuberous Sclerosis 70 0.047
282
P OCL013 Oculodentodigital Dysplasia 69 0.047
283
P HYP086 Hypothyroidism 68 0.047
284
P MYS003 Myasthenia Gravis 68 0.047
285
CNN005 Connective Tissue Disease 66 0.047
286
c WLM013 Wilms Tumor 1 65 0.047
287
P ADN016 Adenocarcinoma 64 0.047
288
P GLM045 Glioma 63 0.047
289
c HPT001 Hepatitis C 63 0.047
290
TXC005 Toxic Shock Syndrome 61 0.047
291
P HYP097 Hyperekplexia 61 0.047
292
P ENC018 Encephalopathy 61 0.047
293
VRL011 Viral Infectious Disease 61 0.047
294
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 0.047
295
P BNG030 Benign Ependymoma 60 0.047
296
STF001 Stiff-Person Syndrome 60 0.047
297
CHC001 Chickenpox 60 0.047
298
c ACT027 Acute Pancreatitis 59 0.047
299
P SZR006 Seizure Disorder 58 0.047
300
CNS004 Constipation 57 0.047
301
P INF032 Infertility 57 0.047
302
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.047
303
APH002 Aphasia 57 0.047
304
THR024 Thrombosis 56 0.047
305
HYP266 Hypoxia 56 0.047
306
INT303 Intracranial Hypertension, Idiopathic 56 0.047
307
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.047
308
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.047
309
PRN019 Perinatal Necrotizing Enterocolitis 54 0.047
310
HMP005 Hemiplegia 54 0.047
311
PNM001 Pneumocystosis 54 0.047
312
PRP016 Paraplegia 53 0.047
313
SNS003 Sensory Peripheral Neuropathy 53 0.047
314
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.047
315
CLL010 Cellular Ependymoma 53 0.047
316
HYP014 Hyperuricemia 51 0.047
317
c ACR116 Aicardi-Goutieres Syndrome 1 51 0.047
318
SPP010 Suppressor of Tumorigenicity 3 51 0.047
319
HRP009 Herpes Simplex Encephalitis 50 0.047
320
c HYP699 Hyperekplexia 1 50 0.047
321
P CTN015 Cutaneous T Cell Lymphoma 49 0.047
322
HDR003 Hidradenitis 49 0.047
323
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.047
324
CHR563 Chronic Eosinophilic Leukemia 48 0.047
325
c CRN241 Corneal Dystrophy, Congenital Stromal 48 0.047
326
GLL048 Glial Tumor 45 0.047
327
EXT010 Extramedullary Plasmacytoma 45 0.047
328
P BNG032 Benign Mesothelioma 45 0.047
329
LTH001 Lethal Midline Granuloma 43 0.047
330
c ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 43 0.047
331
P PRM293 Primary Mediastinal B-Cell Lymphoma 43 0.047
332
TRP014 Triploidy 42 0.047
333
c ATS383 Autosomal Dominant Non-Syndromic Intellectual Disability 1 41 0.047
334
c PRM163 Primary Mediastinal Large B-Cell Lymphoma 41 0.047
335
P RRT020 Rare Tumor 41 0.047
336
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 40 0.047
337
ACT011 Acute Contagious Conjunctivitis 40 0.047
338
ALL014 Allergic Encephalomyelitis 39 0.047
339
c SYS043 Systemic Lupus Erythematosus 1 38 0.047
340
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.047
341
c ADL001 Adult Lymphoma 34 0.047
342
c PRS136 Prostate Cancer, Hereditary, 6 33 0.047
343
PDT001 Pediatric Lymphoma 33 0.047
344
c PRS130 Prostate Cancer, Hereditary, 8 32 0.047
345
RFR002 Refractory Hairy Cell Leukemia 32 0.047
346
HRP011 Herpes Zoster Ophthalmicus 23 0.047
347
P PNC035 Pancreatic Cancer 84 0.038
348
c THR092 Thrombophilia Due to Thrombin Defect 73 0.038
349
c BTT014 Beta-Thalassemia 72 0.038
350
P AMY004 Amyloidosis 70 0.038
351
CRB039 Cerebrovascular Disease 69 0.038
352
PNC129 Pancreatic Adenocarcinoma 67 0.038
353
P HYD006 Hydrocephalus 65 0.038
354
RBR001 Roberts Syndrome 65 0.038
355
PRT036 Peritonitis 65 0.038
356
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.038
357
IDP011 Idiopathic Interstitial Pneumonia 63 0.038
358
P CRN018 Coronary Artery Anomaly 63 0.038
359
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.038
360
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.038
361
c FNC043 Fanconi Anemia, Complementation Group E 62 0.038
362
CLT003 Colitis 62 0.038
363
c ALP101 Alpha-Thalassemia 62 0.038
364
P VSC011 Vasculitis 62 0.038
365
HYD038 Hydrops Fetalis, Nonimmune 61 0.038
366
P PLM036 Pulmonary Fibrosis 61 0.038
367
LNG099 Lung Disease 61 0.038
368
P KDN017 Kidney Cancer 61 0.038
369
ISC004 Ischemia 60 0.038
370
P ALP009 Alopecia Areata 60 0.038
371
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.038
372
P THL005 Thalassemia 60 0.038
373
c HPT016 Hepatitis B 59 0.038
374
P BND020 Bone Disease 59 0.038
375
BRN002 Bronchiolitis 59 0.038
376
VSL002 Visual Epilepsy 58 0.038
377
P OPT006 Optic Nerve Disease 57 0.038
378
P HDC001 Headache 57 0.038
379
c MST023 Mesothelioma, Malignant 57 0.038
380
P CHR640 Charcot-Marie-Tooth Disease, X-Linked Dominant, 1 56 0.038
381
SPN041 Spinal Cord Disease 56 0.038
382
P FBR017 Fibrosarcoma 56 0.038
383
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.038
384
P PLY019 Polyneuropathy 56 0.038
385
BRN012 Bronchiolitis Obliterans 56 0.038
386
HMG005 Hemoglobinopathy 55 0.038
387
c BCT007 Bacterial Meningitis 55 0.038
388
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.038
389
FCT001 Factor Viii Deficiency 55 0.038
390
ANL018 Analbuminemia 54 0.038
391
HMS001 Hemosiderosis 54 0.038
392
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.038
393
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.038
394
ERD001 Erdheim-Chester Disease 52 0.038
395
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.038
396
OCL069 Ocular Motor Apraxia 51 0.038
397
CRY001 Cryptogenic Organizing Pneumonia 51 0.038
398
ASP003 Aseptic Meningitis 51 0.038
399
ACT017 Acute Chest Syndrome 50 0.038
400
c ALM001 Al Amyloidosis 50 0.038
401
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.038
402
P AST007 Astrocytoma 50 0.038
403
DYS073 Dysphagia 50 0.038
404
P SCK005 Sickle Cell Disease 50 0.038
405
INP001 Inappropriate Adh Syndrome 49 0.038
406
MNN009 Meningoencephalitis 49 0.038
407
c INV001 Invasive Aspergillosis 48 0.038
408
PPL021 Papilledema 48 0.038
409
RDC002 Radiculopathy 48 0.038
410
P LYM024 Lymphatic System Disease 48 0.038
411
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.038
412
GLC106 Glucocorticoid Resistance, Generalized 48 0.038
413
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.038
414
P VTR007 Vitreoretinopathy 46 0.038
415
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.038
416
c MLG068 Malignant Glioma 45 0.038
417
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.038
418
IMM136 Immune System Disease 45 0.038
419
P BCT020 Bacteremia 2 44 0.038
420
MRG013 Mirage Syndrome 44 0.038
421
INT253 Intestinal Benign Neoplasm 44 0.038
422
P HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.038
423
c XLN110 X-Linked Charcot-Marie-Tooth Disease 43 0.038
424
PRS063 Paresthesia 43 0.038
425
MDS018 Mediastinal Cancer 42 0.038
426
P AVS003 Avascular Necrosis 42 0.038
427
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.038
428
P RRH023 Rare Hereditary Hemochromatosis 41 0.038
429
c HMG001 Hemoglobin C Disease 40 0.038
430
SPR126 Superior Semicircular Canal Dehiscence 40 0.038
431
P BCL005 B Cell Prolymphocytic Leukemia 39 0.038
432
HMR023 Hemorrhagic Cystitis 38 0.038
433
c HMG029 Hemoglobin Se Disease 38 0.038
434
UNL002 Unilateral Retinoblastoma 37 0.038
435
c WLM011 Wilms Tumor 6 37 0.038
436
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.038
437
SML008 Small Intestine Lymphoma 35 0.038
438
RFR013 Refractory Celiac Disease 35 0.038
439
GRM010 Germ Cells Tumors 34 0.038
440
HDG003 Hodgkin's Lymphoma, Lymphocytic Depletion 33 0.038
441
RRS014 Rare Surgical Neurologic Disease 32 0.038
442
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 32 0.038
443
c ATS385 Autosomal Dominant Non-Syndromic Intellectual Disability 3 30 0.038
444
PNC012 Punctate Epithelial Keratoconjunctivitis 30 0.038
445
INT082 Intraocular Retinoblastoma 29 0.038
446
HRP008 Herpes Simiae 25 0.038
447
c ATS386 Autosomal Dominant Non-Syndromic Intellectual Disability 4 25 0.038
448
EXT029 Extraocular Retinoblastoma 23 0.038
449
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.038
450
CD4008 Cd4/cd8 T-Cell Ratio 20 0.038
451
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.038
452
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.027
453
P ALZ034 Alzheimer Disease 88 0.027
454
P GST053 Gastric Cancer 83 0.027
455
c FNC027 Fanconi Anemia, Complementation Group a 81 0.027
456
P GLM040 Glioma Susceptibility 1 81 0.027
457
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.027
458
P RHM011 Rheumatoid Arthritis 80 0.027
459
STR067 Stroke, Ischemic 80 0.027
460
P BLD134 Bladder Cancer 78 0.027
461
OST012 Osteoarthritis 78 0.027
462
KPS004 Kaposi Sarcoma 75 0.027
463
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.027
464
P OST002 Osteoporosis 73 0.027
465
ANX010 Anxiety 72 0.027
466
P EPL164 Epilepsy 71 0.027
467
P MYC007 Myocardial Infarction 70 0.027
468
WLS001 Wilson Disease 70 0.027
469
P KDN018 Kidney Disease 70 0.027
470
P SLP006 Sleep Apnea 69 0.027
471
P LVR013 Liver Disease 68 0.027
472
OBS002 Obsessive-Compulsive Disorder 68 0.027
473
P MJR001 Major Depressive Disorder 68 0.027
474
P CRD119 Cardiac Arrest 67 0.027
475
P OLG002 Oligodendroglioma 67 0.027
476
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.027
477
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.027
478
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.027
479
HYP056 Hypoglycemia 66 0.027
480
ATH013 Atherosclerosis Susceptibility 66 0.027
481
LNG039 Lung Squamous Cell Carcinoma 65 0.027
482
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.027
483
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.027
484
P DYS154 Dystonia 65 0.027
485
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.027
486
APN008 Apnea, Obstructive Sleep 65 0.027
487
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.027
488
P DBT009 Diabetes Mellitus 64 0.027
489
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.027
490
CLN015 Colon Adenocarcinoma 63 0.027
491
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.027
492
DPR016 Depression 63 0.027
493
LPD008 Lipid Metabolism Disorder 62 0.027
494
P END044 Endometriosis 62 0.027
495
P RHB003 Rhabdomyosarcoma 62 0.027
496
P ART023 Arthropathy 62 0.027
497
P HML002 Hemolytic Anemia 62 0.027
498
P PSR002 Psoriasis 62 0.027
499
MNN042 Meningioma, Radiation-Induced 62 0.027
500
P ESP024 Esophagitis 62 0.027
501
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.027
502
P DRM010 Dermatomyositis 61 0.027
503
DRM006 Dermatitis 61 0.027
504
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.027
505
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.027
506
SPN186 Spinal Cord Injury 60 0.027
507
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.027
508
CRD223 Cardiac Arrhythmia 60 0.027
509
DCB001 Decubitus Ulcer 60 0.027
510
SQM006 Squamous Cell Carcinoma 60 0.027
511
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.027
512
P MYC008 Myocarditis 59 0.027
513
GST045 Gastroenteritis 59 0.027
514
IGR001 Ige Responsiveness, Atopic 59 0.027
515
PLM033 Pulmonary Embolism 59 0.027
516
P BRS044 Breast Adenocarcinoma 59 0.027
517
CHL067 Cholecystitis 58 0.027
518
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.027
519
PST028 Post-Traumatic Stress Disorder 58 0.027
520
NWB001 Newborn Respiratory Distress Syndrome 58 0.027
521
DSS008 Disease of Mental Health 57 0.027
522
PLG002 Plague 57 0.027
523
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.027
524
MNT002 Mental Depression 57 0.027
525
P GLM007 Glomerulonephritis 57 0.027
526
TRN018 Transitional Cell Carcinoma 56 0.027
527
AGN016 Aging 56 0.027
528
PNM008 Pneumothorax 56 0.027
529
P GST044 Gastritis 55 0.027
530
BRN004 Brain Edema 55 0.027
531
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.027
532
PYD001 Pyoderma Gangrenosum 54 0.027
533
END040 Endogenous Depression 54 0.027
534
P LNG035 Lung Large Cell Carcinoma 54 0.027
535
PST046 Post-Transplant Lymphoproliferative Disease 53 0.027
536
INT075 Intracranial Hypertension 53 0.027
537
P TRM003 Tremor 53 0.027
538
KRT006 Keratoconjunctivitis 53 0.027
539
P PNC025 Panic Disorder 53 0.027
540
NRT001 Neurotic Disorder 52 0.027
541
ACR041 Acromelic Frontonasal Dysostosis 52 0.027
542
P HMR003 Hemorrhagic Disease 52 0.027
543
P SML001 Small Cell Carcinoma 52 0.027
544
PST011 Pustulosis of Palm and Sole 52 0.027
545
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 52 0.027
546
P INS002 in Situ Carcinoma 52 0.027
547
OVR059 Ovary Adenocarcinoma 51 0.027
548
PYD002 Pyoderma 51 0.027
549
ILS001 Ileus 51 0.027
550
CHR635 Chromosome 5q Deletion Syndrome 51 0.027
551
BLD053 Blood Platelet Disease 51 0.027
552
AZS001 Azoospermia 50 0.027
553
HYP081 Hypolipoproteinemia 50 0.027
554
P THR015 Thrombophilia 50 0.027
555
LNG031 Lung Benign Neoplasm 50 0.027
556
CLR109 Colorectal Adenocarcinoma 50 0.027
557
DYS015 Dysentery 50 0.027
558
c INF145 Infantile Liver Failure Syndrome 1 50 0.027
559
CSY001 C Syndrome 50 0.027
560
P PRT096 Peritoneal Mesothelioma 50 0.027
561
PNM005 Pneumonic Plague 50 0.027
562
HYP017 Hypophosphatemia 49 0.027
563
BRN071 Brain Injury 49 0.027
564
CHL004 Cholelithiasis 49 0.027
565
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.027
566
VCC001 Vaccinia 49 0.027
567
HMG002 Hemoglobinuria 49 0.027
568
BNR002 Bone Resorption Disease 48 0.027
569
CHL056 Cheilitis 48 0.027
570
CRD137 Cardiogenic Shock 48 0.027
571
CLC006 Calcinosis 48 0.027
572
FCL012 Facial Paralysis 48 0.027
573
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.027
574
ACT084 Acute Stress Disorder 48 0.027
575
c HMN021 Human T-Cell Leukemia Virus Type 1 48 0.027
576
RGH001 Right Bundle Branch Block 47 0.027
577
SPN021 Spinal Meningioma 47 0.027
578
c LRG017 Large Intestine Cancer 47 0.027
579
CLS016 Clostridium Difficile Colitis 46 0.027
580
P PLY020 Polyradiculoneuropathy 46 0.027
581
ANP006 Anaplastic Ependymoma 46 0.027
582
P MTH007 Methemoglobinemia 46 0.027
583
MCS004 Mucosal Melanoma 46 0.027
584
TRT001 Teratocarcinoma 46 0.027
585
SYN036 Syncope 45 0.027
586
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.027
587
c MYL058 Myeloproliferative Syndrome, Transient 44 0.027
588
SBC016 Subacute Delirium 44 0.027
589
P CMM008 Communicating Hydrocephalus 43 0.027
590
IRT001 Iritis 43 0.027
591
ANP009 Anaplastic Oligodendroglioma 43 0.027
592
DRG002 Drug-Induced Hepatitis 42 0.027
593
PST053 Postherpetic Neuralgia 42 0.027
594
c MLG079 Malignant Pleural Mesothelioma 42 0.027
595
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.027
596
GST020 Gastric Antral Vascular Ectasia 41 0.027
597
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 41 0.027
598
LRG008 Large Granular Lymphocyte Leukemia 41 0.027
599
GLC008 Glucose Metabolism Disease 40 0.027
600
GRM004 Germinoma 40 0.027
601
PLY100 Polyploidy 40 0.027
602
HST016 Histiocytic Sarcoma 39 0.027
603
LYM116 Lymph Node Disease 39 0.027
604
BRC011 Brachial Plexus Neuropathy 39 0.027
605
CHL039 Choledocholithiasis 39 0.027
606
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.027
607
c OVR114 Ovarian Cancer 1 38 0.027
608
RHB002 Rhabdoid Meningioma 38 0.027
609
SWL001 Swallowing Disorders 38 0.027
610
SCR001 Secretory Meningioma 37 0.027
611
P CRB045 Cerebellar Hypoplasia 37 0.027
612
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.027
613
NNL001 Non-Langerhans-Cell Histiocytosis 37 0.027
614
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.027
615
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.027
616
OLG006 Oligoastrocytoma 35 0.027
617
BRK012 Broken Heart Syndrome 35 0.027
618
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.027
619
NNN007 Non-Involuting Congenital Hemangioma 33 0.027
620
SGT001 Sagittal Sinus Thrombosis 32 0.027
621
FML031 Female Stress Incontinence 32 0.027
622
HPT085 Hepatitis, Fulminant Viral 32 0.027
623
c DRR009 Diarrhea 6 32 0.027
624
CYT004 Cytomegalic Inclusion Disease 31 0.027
625
MNN010 Meningeal Melanoma 31 0.027
626
MRK002 Marek Disease 31 0.027
627
MXD032 Mixed Germ Cell Tumor 31 0.027
628
MNN008 Meningeal Melanomatosis 30 0.027
629
PRN008 Peroneal Nerve Paralysis 30 0.027
630
MLN002 Melanomatosis 29 0.027
631
PST092 Posttransplant Acute Limbic Encephalitis 29 0.027
632
c DRR018 Diarrhea 9 29 0.027
633
FLL042 Folliculotropic Mycosis Fungoides 28 0.027
634
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.027
635
c VRL008 Viral Exanthem 25 0.027
636
HMP028 Hemophagocytic Syndrome Associated with an Infection 24 0.027
637
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 22 0.027
638
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 20 0.027
640
IDP081 Idiopathic Hypertrophic Pachymeningitis 18 0.027
641
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 16 0.027
642
SYR007 Syringohydromyelia 15 0.027
643
c RFR015 Refractory Anemia with Excess Blasts Type 1 15 0.027
644
PNF002 Painful Legs and Moving Toes Syndrome 14 0.027
645
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 14 0.027
646
UNC013 Unclassified Acute Myeloid Leukemia 4 0.027
Content
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