Search results for Fludarabine

834 hits were found for Fludarabine

# Family MCID Name MIFTS Score
1
P LYM031 Lymphocytic Leukemia 56 0.837
2
P LKM002 Leukemia 69 0.770
3
c LKM071 Leukemia, Chronic Lymphocytic 81 0.766
4
c LKM004 Leukemia, B-Cell, Chronic 35 0.729
5
P GRF003 Graft-Versus-Host Disease 71 0.658
6
P LYM118 Lymphoma 70 0.619
7
c LKM061 Leukemia, Acute Myeloid 84 0.604
8
P MYL006 Myeloid Leukemia 61 0.594
9
LYM019 Lymphosarcoma 48 0.571
10
MYL009 Myelodysplastic Syndrome 72 0.550
11
HMT018 Hematopoietic Stem Cell Transplantation 54 0.465
12
c CHR064 Chronic Monocytic Leukemia 43 0.456
13
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.447
14
LYM133 Lymphoma, Hodgkin, Classic 70 0.442
15
P LKM062 Leukemia, Acute Lymphoblastic 68 0.441
16
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.432
17
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.423
18
c ACT135 Acute Graft Versus Host Disease 52 0.417
19
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.395
20
DFC004 Deficiency Anemia 77 0.387
21
c LKM063 Leukemia, Chronic Myeloid 74 0.386
22
LYM040 Lymphoblastic Lymphoma 54 0.382
23
P FLL037 Follicular Lymphoma 67 0.380
24
HMT002 Hematologic Cancer 64 0.373
25
MYL069 Myeloma, Multiple 85 0.372
26
c CHR417 Chronic Graft Versus Host Disease 56 0.370
27
P BCL017 B-Cell Lymphoma 61 0.352
28
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.339
29
c ACT073 Acute Leukemia 59 0.338
30
MNT001 Mantle Cell Lymphoma 69 0.335
31
c FLL041 Follicular Lymphoma 1 50 0.312
32
HML018 Homologous Wasting Disease 22 0.308
33
P NTR004 Neutropenia 64 0.304
34
c PRM038 Primary Agammaglobulinemia 45 0.304
35
P CNR004 Cone-Rod Dystrophy 2 72 0.303
36
P APL001 Aplastic Anemia 76 0.294
37
MYL031 Myeloproliferative Neoplasm 66 0.294
38
MCR004 Macroglobulinemia 50 0.291
39
BNM001 Bone Marrow Cancer 48 0.287
40
ADL002 Adult Syndrome 62 0.268
41
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.265
42
MRG003 Marginal Zone B-Cell Lymphoma 55 0.261
43
LYM012 Lymphoplasmacytic Lymphoma 62 0.258
44
RTC005 Reticulosarcoma 48 0.258
45
P CHR285 Chronic Myelomonocytic Leukemia 60 0.257
47
P TRN020 Turner Syndrome 66 0.254
48
MYL005 Myelofibrosis 69 0.253
49
BRK010 Burkitt Lymphoma 68 0.249
50
P SRC025 Sarcoidosis 1 72 0.247
51
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.247
52
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.247
53
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 28 0.247
54
HDG004 Hodgkin's Granuloma 27 0.247
55
HDG006 Hodgkin's Paragranuloma 23 0.247
56
c RHB024 Rhabdomyosarcoma 2 64 0.236
57
RFR010 Refractory Anemia 50 0.232
58
SKN019 Skin Melanoma 68 0.230
59
MLN008 Melanoma 68 0.230
60
PLS025 Plasmablastic Lymphoma 48 0.215
61
c JVN004 Juvenile Myelomonocytic Leukemia 68 0.214
62
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.214
63
IMM167 Immune Deficiency Disease 79 0.210
64
PRL017 Prolymphocytic Leukemia 45 0.210
65
MYL075 Myelodysplastic/myeloproliferative Neoplasm 50 0.204
66
MYC006 Mycosis Fungoides 67 0.193
67
c FNC027 Fanconi Anemia, Complementation Group a 81 0.191
68
P TCL004 T-Cell Leukemia 48 0.191
69
c LKM005 Leukemia, T-Cell, Chronic 35 0.191
70
DWN001 Down Syndrome 70 0.190
71
P THR014 Thrombocytopenia 67 0.187
72
P LYM033 Lymphoproliferative Syndrome 62 0.187
73
SPL004 Splenic Marginal Zone Lymphoma 48 0.183
74
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.182
75
c ADL017 Adult T-Cell Leukemia 59 0.180
76
DFF005 Diffuse Large B-Cell Lymphoma 56 0.180
77
PLS011 Plasmacytoma 57 0.177
78
MYL074 Myelodysplastic Syndrome with Excess Blasts 37 0.177
79
SZR001 Sezary's Disease 59 0.174
80
ATY042 Atypical Chronic Myeloid Leukemia 50 0.170
81
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.169
82
c CHR418 Chronic Leukemia 52 0.169
83
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.163
84
CNG028 Congenital Hypoplastic Anemia 46 0.163
85
PLY001 Polycythemia Vera 70 0.162
86
P PLY018 Polycythemia 56 0.162
87
c PRM012 Primary Polycythemia 52 0.162
88
FCT007 Factor Vii Deficiency 65 0.160
89
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.160
90
CYT002 Cytokine Deficiency 46 0.160
91
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 56 0.158
92
MCS002 Mucositis 56 0.158
93
PLS016 Plasma Cell Leukemia 41 0.158
94
48X005 48,xyyy 37 0.158
95
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 27 0.158
96
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.156
97
LYM027 Lymphopenia 58 0.156
98
LYM051 Lymphomatoid Granulomatosis 47 0.156
99
HRY003 Hairy Cell Leukemia 57 0.152
100
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.152
101
P CTN015 Cutaneous T Cell Lymphoma 52 0.150
102
ANG046 Angioimmunoblastic T-Cell Lymphoma 49 0.150
103
HPT046 Hepatic Veno-Occlusive Disease 56 0.148
104
P SCK005 Sickle Cell Disease 53 0.148
105
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.148
106
ALL026 Allergic Hypersensitivity Disease 65 0.147
107
P FNC004 Fanconi Syndrome 48 0.145
108
CLL014 Cll/sll 44 0.145
109
P ESS003 Essential Thrombocythemia 69 0.143
110
c THR090 Thrombocythemia 1 47 0.143
111
P HML002 Hemolytic Anemia 64 0.140
112
CYS036 Cystinosis, Nephropathic 53 0.140
113
PNC001 Pancytopenia 54 0.138
114
P KDN017 Kidney Cancer 60 0.136
115
ATX019 Ataxia with Vitamin E Deficiency 46 0.136
116
SCK003 Sickle Cell Anemia 74 0.134
117
ACT216 Acute Leukemia of Ambiguous Lineage 35 0.134
118
c TCL024 T-Cell Non-Hodgkin Lymphoma 37 0.132
119
TCL002 T-Cell Large Granular Lymphocyte Leukemia 46 0.130
120
GRN017 Granulocytopenia 46 0.130
121
P THL005 Thalassemia 62 0.127
122
PRP036 Peripheral T-Cell Lymphoma 53 0.127
123
c HMG029 Hemoglobin Se Disease 40 0.127
124
SPR126 Superior Semicircular Canal Dehiscence 39 0.127
125
HMG005 Hemoglobinopathy 57 0.125
126
P OVR042 Ovarian Cancer 89 0.123
127
c CHR682 Chronic Bilirubin Encephalopathy 36 0.123
128
MGK001 Megakaryocytic Leukemia 65 0.120
129
P ANP001 Anaplastic Large Cell Lymphoma 62 0.120
130
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 58 0.120
131
HMG002 Hemoglobinuria 49 0.120
132
LRG008 Large Granular Lymphocyte Leukemia 45 0.120
133
SRC014 Sarcoma 67 0.118
134
c ANM038 Anemia, Autoimmune Hemolytic 61 0.118
135
ERY051 Erythroleukemia, Familial 58 0.118
136
P BCL004 B-Cell Non-Hodgkin Lymphoma 38 0.118
137
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.116
138
CHR286 Chronic Neutrophilic Leukemia 36 0.116
139
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 34 0.116
140
CLS052 Classic Hairy Cell Leukemia 28 0.116
141
BND002 B- and T-Cell Mixed Leukemia 19 0.116
142
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.113
143
SVR004 Severe Combined Immunodeficiency 74 0.113
144
c ALP101 Alpha-Thalassemia 63 0.113
145
VRL011 Viral Infectious Disease 62 0.113
146
SPN035 Spindle Cell Sarcoma 57 0.113
147
SFT003 Soft Tissue Sarcoma 57 0.110
148
c MLG074 Malignant Mesenchymoma 50 0.110
149
SKN013 Skin Benign Neoplasm 49 0.110
150
c OVR114 Ovarian Cancer 1 39 0.110
151
P PNM007 Pneumonia 71 0.108
152
P EXN002 Exanthem 58 0.108
153
CHR563 Chronic Eosinophilic Leukemia 49 0.108
154
RCH001 Richter's Syndrome 47 0.108
155
INT054 Intraocular Lymphoma 45 0.108
156
EXT048 Extranodal Nasal Nk/t Cell Lymphoma 37 0.108
157
P CHR012 Chronic Granulomatous Disease 69 0.105
158
P SKN015 Skin Carcinoma 67 0.105
159
P BRS047 Breast Cancer 99 0.102
160
P HMP002 Hemophagocytic Lymphohistiocytosis 68 0.102
161
SQM006 Squamous Cell Carcinoma 60 0.102
162
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.102
163
SPL018 Splenomegaly 48 0.102
164
NTR003 Natural Killer Cell Leukemia 44 0.102
165
P NRB010 Neuroblastoma 1 66 0.099
166
P CYS018 Cystitis 59 0.099
167
c LKM070 Leukemia, Acute Monocytic 55 0.099
168
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.099
169
P DYS007 Dyskeratosis Congenita 64 0.096
170
P SZR006 Seizure Disorder 59 0.096
171
P DRR001 Diarrhea 55 0.096
172
47X002 47,xyy 49 0.096
173
ACT098 Acute Erythroid Leukemia 48 0.096
174
P DMN001 Diamond-Blackfan Anemia 69 0.093
175
CHL079 Children's Interstitial Lung Disease 27 0.093
176
P LNG032 Lung Cancer 99 0.090
177
c BTT014 Beta-Thalassemia 73 0.090
178
P KDN018 Kidney Disease 73 0.090
179
P HYP098 Hypereosinophilic Syndrome 67 0.090
180
ACT119 Acute Promyelocytic Leukemia 63 0.090
181
HRP004 Herpes Zoster 58 0.090
182
c MLG054 Malignant Histiocytosis 51 0.090
183
CMB081 Combined Immunodeficiency, X-Linked 47 0.090
184
RDC006 Red Cell Aplasia 45 0.090
185
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.087
186
c HPT016 Hepatitis B 63 0.087
187
P ALP008 Alopecia 58 0.087
188
PST046 Post-Transplant Lymphoproliferative Disease 55 0.087
189
P MNC007 Monocytic Leukemia 52 0.087
190
P PRR002 Pure Red-Cell Aplasia 47 0.087
191
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.087
192
HMR023 Hemorrhagic Cystitis 40 0.087
193
CHR178 Chromosomal Triplication 36 0.087
194
c ADL093 Adult Acute Monocytic Leukemia 20 0.087
195
P PNC035 Pancreatic Cancer 86 0.083
196
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.083
197
CRV035 Cervical Cancer 77 0.083
198
ADR007 Adrenoleukodystrophy 72 0.083
199
P WSK001 Wiskott-Aldrich Syndrome 71 0.083
200
P HPT021 Hepatitis 69 0.083
201
CNG034 Congestive Heart Failure 69 0.083
202
c SML038 Small Cell Cancer of the Lung 67 0.083
203
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.083
204
ACT200 Acute Monoblastic Leukemia 56 0.083
205
PRG009 Progressive Multifocal Leukoencephalopathy 55 0.083
206
c DMN023 Diamond-Blackfan Anemia 1 51 0.083
207
TRP009 Triple X Syndrome 42 0.083
208
ACT114 Acute Myeloblastic Leukemia Without Maturation 34 0.083
209
RFR009 Refractory Cytopenia with Multilineage Dysplasia 32 0.083
210
P CLR023 Colorectal Cancer 100 0.080
211
P HPT023 Hepatocellular Carcinoma 99 0.080
212
c SYS001 Systemic Lupus Erythematosus 88 0.080
213
P AMY004 Amyloidosis 71 0.080
214
ATM095 Autoimmune Disease 62 0.080
215
SPN041 Spinal Cord Disease 57 0.080
216
IMM136 Immune System Disease 52 0.080
217
THR004 Thrombocytosis 52 0.080
218
c ALM001 Al Amyloidosis 50 0.080
219
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 46 0.080
220
MRG013 Mirage Syndrome 42 0.080
221
RFR002 Refractory Hairy Cell Leukemia 32 0.080
222
PLS003 Plasmacytic Leukemia 26 0.080
223
P ART022 Arthritis 71 0.076
224
P LVR013 Liver Disease 71 0.076
225
P ADN016 Adenocarcinoma 65 0.076
226
P LPS004 Lupus Erythematosus 62 0.076
227
LNG108 Langerhans Cell Histiocytosis 60 0.076
228
P HST010 Histiocytosis 54 0.076
229
GLB002 Glioblastoma 74 0.072
230
GLB015 Glioblastoma Multiforme 60 0.072
231
P INF032 Infertility 60 0.072
232
P NRP001 Neuropathy 57 0.072
233
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.072
234
DYS164 Dyskeratosis Congenita, X-Linked 54 0.072
235
c INH020 Inherited Metabolic Disorder 51 0.072
236
c TCL005 T-Cell Prolymphocytic Leukemia 50 0.072
237
MST002 Mast-Cell Leukemia 49 0.072
238
P BCL005 B Cell Prolymphocytic Leukemia 40 0.072
239
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.068
240
P HRT032 Heart Disease 78 0.068
241
P RSP003 Respiratory Failure 75 0.068
242
HMN044 Human Immunodeficiency Virus Type 1 73 0.068
243
P GLM040 Glioma Susceptibility 1 68 0.068
244
P ENC018 Encephalopathy 64 0.068
245
P PSR002 Psoriasis 63 0.068
246
NTR005 Nutritional Deficiency Disease 61 0.068
247
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.068
248
TXC002 Toxic Encephalopathy 54 0.068
249
CHC001 Chickenpox 53 0.068
250
STM007 Stomatitis 51 0.068
251
PST011 Pustulosis of Palm and Sole 51 0.068
252
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.068
253
CHR208 Chromosome 17p Deletion 23 0.068
254
HDG009 Hodgkin Lymphoma, Childhood 20 0.068
255
ESP021 Esophageal Cancer 90 0.064
256
P RHM011 Rheumatoid Arthritis 82 0.064
257
P OST001 Osteopetrosis 70 0.064
258
P SYS005 Systemic Scleroderma 68 0.064
259
CHD001 Chediak-Higashi Syndrome 68 0.064
260
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.064
261
OST159 Osteogenic Sarcoma 67 0.064
262
P AGM001 Agammaglobulinemia 66 0.064
263
P HRP006 Herpes Simplex 66 0.064
264
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.064
265
P PRP019 Peripheral Nervous System Disease 64 0.064
266
FLL027 Fallopian Tube Carcinoma 64 0.064
267
LNG099 Lung Disease 62 0.064
268
ISC004 Ischemia 62 0.064
269
c SCL052 Scleroderma, Familial Progressive 62 0.064
270
ACQ007 Acquired Immunodeficiency Syndrome 61 0.064
271
c ACT071 Acute Kidney Failure 60 0.064
272
c MCL013 Mucolipidosis Iv 60 0.064
273
P GLM007 Glomerulonephritis 58 0.064
274
VSL002 Visual Epilepsy 58 0.064
275
IRN002 Iron Metabolism Disease 58 0.064
276
BLR008 Bilirubin Metabolic Disorder 58 0.064
277
BCT022 Bacterial Infectious Disease 57 0.064
278
CMR002 Coumarin Resistance 56 0.064
279
PPL022 Papilloma 56 0.064
280
PNM001 Pneumocystosis 53 0.064
281
MNC006 Monoclonal Gammopathy of Uncertain Significance 50 0.064
282
P LPM005 Lipomatosis 49 0.064
283
SQM002 Squamous Cell Papilloma 49 0.064
284
EXC002 Exocrine Pancreatic Insufficiency 41 0.064
285
49X002 49,xxxxy Syndrome 39 0.064
286
c SYS043 Systemic Lupus Erythematosus 1 39 0.064
287
ATM052 Autoimmune Disease 1 38 0.064
288
LTT002 Letterer-Siwe Disease 36 0.064
289
RFR004 Refractory Hematologic Cancer 27 0.064
290
FTL073 Fetal Anticonvulsant Syndrome 26 0.064
291
P GST053 Gastric Cancer 85 0.059
292
P BLD134 Bladder Cancer 79 0.059
293
CRB039 Cerebrovascular Disease 71 0.059
294
EWN003 Ewing Sarcoma 69 0.059
295
CMM004 Common Variable Immunodeficiency 69 0.059
296
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.059
297
P NPH012 Nephrotic Syndrome 65 0.059
298
P RHB003 Rhabdomyosarcoma 62 0.059
299
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.059
300
P ALP009 Alopecia Areata 61 0.059
301
SRC027 Sarcoma, Synovial 60 0.059
302
c SVR003 Severe Congenital Neutropenia 59 0.059
303
c MST023 Mesothelioma, Malignant 59 0.059
304
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.059
305
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.059
306
P PMP001 Pemphigus 56 0.059
307
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 55 0.059
308
HRL003 Hurler Syndrome 55 0.059
309
NTR018 Neutrophilia, Hereditary 53 0.059
310
LNG031 Lung Benign Neoplasm 52 0.059
311
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 52 0.059
312
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 51 0.059
313
c OST131 Osteopetrosis, Autosomal Dominant 2 51 0.059
314
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.059
315
GLL048 Glial Tumor 48 0.059
316
P BNG032 Benign Mesothelioma 47 0.059
317
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.059
318
DFF003 Diffuse Scleroderma 43 0.059
319
ADR022 Adrenomyeloneuropathy 39 0.059
320
OVR094 Ovarian Epithelial Cancer 39 0.059
321
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.059
323
P ATX030 Ataxia-Telangiectasia 83 0.054
324
STR067 Stroke, Ischemic 82 0.054
325
BRN028 Brain Cancer 75 0.054
326
c WLM013 Wilms Tumor 1 69 0.054
327
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.054
328
P GLM045 Glioma 64 0.054
329
c ACT068 Acute Cystitis 63 0.054
330
c WLM018 Wilms Tumor 5 63 0.054
331
TXC005 Toxic Shock Syndrome 63 0.054
332
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.054
333
MRK001 Merkel Cell Carcinoma 62 0.054
334
c HPT001 Hepatitis C 62 0.054
335
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 59 0.054
336
PRP030 Purpura 56 0.054
337
c PSR017 Psoriasis 2 55 0.054
338
P PLY019 Polyneuropathy 55 0.054
339
LST001 Listeriosis 55 0.054
340
HMS001 Hemosiderosis 54 0.054
341
TLN003 Telangiectasis 53 0.054
342
c LRG017 Large Intestine Cancer 53 0.054
343
VGN017 Vaginal Cancer 51 0.054
344
c PSR023 Psoriasis 1 50 0.054
345
MYL003 Myeloid Sarcoma 50 0.054
346
CLD007 Cold Agglutinin Disease 47 0.054
347
EXT010 Extramedullary Plasmacytoma 46 0.054
348
TCL003 T Cell Deficiency 44 0.054
349
PRN049 Paraneoplastic Pemphigus 43 0.054
350
GST071 Gastrointestinal Carcinoma 42 0.054
351
P HYP073 Hypersensitivity Reaction Type Iv Disease 42 0.054
352
CHR492 Chromosome 13q14 Deletion Syndrome 42 0.054
353
THR123 Thrombotic Microangiopathy 41 0.054
354
P PRM293 Primary Mediastinal B-Cell Lymphoma 41 0.054
355
P RRH023 Rare Hereditary Hemochromatosis 41 0.054
356
c PSR028 Psoriasis 7 40 0.054
357
c PSR018 Psoriasis 13 40 0.054
358
c PSR032 Psoriasis 11 40 0.054
359
IND016 Indolent B-Cell Non-Hodgkin Lymphoma 36 0.054
360
ACT118 Acute Non Lymphoblastic Leukemia 27 0.054
361
CRH001 Crohn's Disease 75 0.048
362
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.048
363
P RTN024 Retinoblastoma 74 0.048
364
P MLT020 Multiple Sclerosis 73 0.048
365
P MLN066 Melanoma, Cutaneous Malignant 1 69 0.048
366
P PLM037 Pulmonary Hypertension 69 0.048
367
P INF038 Influenza 69 0.048
368
SCH036 Scheie Syndrome 68 0.048
369
P NSP012 Nasopharyngeal Carcinoma 67 0.048
370
P ASP006 Aspergillosis 67 0.048
371
P MNN013 Meningitis 67 0.048
372
LKC009 Leukocyte Adhesion Deficiency, Type I 64 0.048
373
P VSC011 Vasculitis 64 0.048
374
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.048
375
PSR001 Psoriatic Arthritis 63 0.048
376
c MNN047 Mannosidosis, Alpha B, Lysosomal 63 0.048
377
CRC021 Carcinosarcoma 62 0.048
378
P CTR002 Cataract 62 0.048
379
DGR001 Digeorge Syndrome 61 0.048
380
STT001 Status Epilepticus 61 0.048
381
DPH001 Diphtheria 61 0.048
382
RBR001 Roberts Syndrome 61 0.048
383
IMM174 Immunodeficiency with Hyper-Igm, Type 1 60 0.048
384
P MLN069 Melanoma, Uveal 59 0.048
385
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 58 0.048
386
TRN018 Transitional Cell Carcinoma 57 0.048
387
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.048
388
OCL022 Ocular Melanoma 54 0.048
389
P EPD016 Epidermolysis Bullosa 54 0.048
390
c ACT020 Acute T Cell Leukemia 54 0.048
391
CLR030 Clear Cell Renal Cell Carcinoma 54 0.048
392
HYP014 Hyperuricemia 52 0.048
393
VLC001 Velocardiofacial Syndrome 50 0.048
394
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.048
395
GST049 Gastrointestinal System Cancer 49 0.048
396
CHL061 Childhood Leukemia 49 0.048
397
ANS011 Anus Cancer 49 0.048
398
JCB001 Jacobsen Syndrome 48 0.048
399
LYM024 Lymphatic System Disease 48 0.048
400
c OPT050 Opitz Gbbb Syndrome, Type Ii 48 0.048
401
CRY004 Cryoglobulinemia 47 0.048
402
ACT017 Acute Chest Syndrome 47 0.048
403
c FML008 Familial Retinoblastoma 46 0.048
404
CRB138 Core Binding Factor Acute Myeloid Leukemia 43 0.048
405
P AVS003 Avascular Necrosis 43 0.048
406
CD4003 Cd40 Ligand Deficiency 43 0.048
407
c ADL052 Adult Acute Lymphocytic Leukemia 42 0.048
408
LKP003 Leukoplakia 40 0.048
409
MXD023 Mixed Cell Type Cancer 38 0.048
410
c WLM011 Wilms Tumor 6 38 0.048
411
NDL024 Nodal Marginal Zone Lymphoma 37 0.048
412
ACT177 Acute Basophilic Leukemia 35 0.048
413
P PLY188 Polyendocrinopathy 35 0.048
414
GRM010 Germ Cells Tumors 35 0.048
415
ANS025 Anus Benign Neoplasm 34 0.048
416
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 34 0.048
417
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 31 0.048
418
P PRS040 Prostate Cancer 97 0.042
419
c ATR087 Atrial Standstill 1 76 0.042
420
END057 Endometrial Cancer 74 0.042
421
P MYC007 Myocardial Infarction 74 0.042
422
c MNN043 Meningioma, Familial 74 0.042
423
c SPN225 Spondyloarthropathy 1 74 0.042
424
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.042
425
P MYC084 Mycobacterium Tuberculosis 1 69 0.042
426
P MTC003 Metachromatic Leukodystrophy 69 0.042
427
CHL065 Cholangiocarcinoma 68 0.042
428
P KRB001 Krabbe Disease 68 0.042
429
P NRV007 Nervous System Disease 68 0.042
430
c BSL007 Basal Cell Carcinoma 68 0.042
431
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.042
432
P PLM036 Pulmonary Fibrosis 66 0.042
433
LNG039 Lung Squamous Cell Carcinoma 66 0.042
434
P VSC007 Vascular Disease 65 0.042
435
MST024 Mastocytosis, Cutaneous 65 0.042
436
IDP011 Idiopathic Interstitial Pneumonia 65 0.042
437
MNN042 Meningioma, Radiation-Induced 64 0.042
438
SKN016 Skin Disease 64 0.042
439
CLT003 Colitis 63 0.042
440
c MCP050 Mucopolysaccharidosis, Type Ii 63 0.042
441
SVR066 Severe Combined Immunodeficiency, X-Linked 62 0.042
442
BLD131 Bladder Urothelial Carcinoma 62 0.042
443
TTN003 Tetanus 62 0.042
444
LKD001 Leukodystrophy 61 0.042
445
P SHW006 Shwachman-Diamond Syndrome 1 61 0.042
446
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.042
447
P PNL012 Penile Cancer 61 0.042
448
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.042
449
PNM010 Pneumothorax, Primary Spontaneous 60 0.042
450
END030 End Stage Renal Failure 60 0.042
451
GST045 Gastroenteritis 60 0.042
452
CYT008 Cytomegalovirus Infection 58 0.042
453
HYP266 Hypoxia 58 0.042
454
P INF037 Inflammatory Bowel Disease 57 0.042
455
P CHN012 Chondrosarcoma 57 0.042
456
BRN004 Brain Edema 57 0.042
457
RHM027 Rheumatic Disease 56 0.042
458
P BNC003 Bone Cancer 56 0.042
459
PNM008 Pneumothorax 56 0.042
460
P MCR010 Microcephaly 56 0.042
461
c INT072 Intestinal Pseudo-Obstruction 55 0.042
462
SYN007 Synovitis 55 0.042
463
c CNG208 Congenital Disorder of Glycosylation, Type Iic 55 0.042
464
P TRM003 Tremor 55 0.042
465
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 55 0.042
466
INT079 Intrahepatic Cholangiocarcinoma 54 0.042
467
P MMB011 Membranous Nephropathy 54 0.042
468
AMN001 Amenorrhea 54 0.042
469
SPP010 Suppressor of Tumorigenicity 3 54 0.042
470
MCS006 Macs Syndrome 54 0.042
471
VLV032 Vulva Cancer 53 0.042
472
c ACT134 Acute Liver Failure 53 0.042
473
OCL069 Ocular Motor Apraxia 53 0.042
474
GLS018 Glass Syndrome 51 0.042
475
INT253 Intestinal Benign Neoplasm 50 0.042
476
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.042
477
ADN009 Adenosquamous Carcinoma 50 0.042
478
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 50 0.042
479
MTB004 Metabolic Acidosis 48 0.042
480
BNG036 Bone Giant Cell Tumor 48 0.042
481
HST009 Histiocytoma 47 0.042
482
PNN001 Panniculitis 47 0.042
483
c BSL024 Basal Cell Carcinoma 1 47 0.042
484
CRY014 Cryptococcal Meningitis 46 0.042
485
c MLG068 Malignant Glioma 46 0.042
486
MLG065 Malignant Fibroxanthoma 45 0.042
487
P GNT008 Giant Cell Tumor 45 0.042
488
PRT035 Peritoneum Cancer 45 0.042
489
BNS007 Bone Sarcoma 44 0.042
490
LYM052 Lymphomatoid Papulosis 43 0.042
491
c MLG079 Malignant Pleural Mesothelioma 43 0.042
492
P PRT026 Parotitis 43 0.042
493
P DMY001 Demyelinating Polyneuropathy 43 0.042
494
HRL004 Hurler-Scheie Syndrome 43 0.042
495
OVR112 Ovarian Germ Cell Cancer 43 0.042
496
ORL012 Oral Leukoplakia 42 0.042
497
GST020 Gastric Antral Vascular Ectasia 42 0.042
498
IMM078 Immunodeficiency 21 41 0.042
499
SPN021 Spinal Meningioma 40 0.042
500
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.042
501
c PST022 Posterior Uveal Melanoma 39 0.042
502
MCP033 Mucopolysaccharidoses 39 0.042
503
c MYL058 Myeloproliferative Syndrome, Transient 39 0.042
504
SCR001 Secretory Meningioma 38 0.042
505
SYS071 Systemic Autoimmune Disease 38 0.042
506
P HVY001 Heavy Chain Disease 38 0.042
507
SML008 Small Intestine Lymphoma 37 0.042
508
MXD026 Mixed Glioma 36 0.042
509
c PRS136 Prostate Cancer, Hereditary, 6 34 0.042
510
c PRS130 Prostate Cancer, Hereditary, 8 33 0.042
511
MYC088 Mycobacterium Avium Complex Infections 30 0.042
512
TMR016 Tumor Suppressor Gene on Chromosome 11 29 0.042
513
c THR110 Thrombocytopenia 6 29 0.042
514
MLG164 Malignant Epithelial Tumor of Ovary 27 0.042
515
PGM030 Pigmentation Anomaly of the Skin 26 0.042
516
IND005 Indolent B Cell Lymphoma 21 0.042
517
c BSL027 Basal Cell Carcinoma 4 17 0.042
518
c HYP595 Hypertension, Essential 87 0.034
519
PFF001 Pfeiffer Syndrome 79 0.034
520
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.034
521
ANX010 Anxiety 75 0.034
522
PRP027 Peripheral Vascular Disease 72 0.034
523
AGM019 Agammaglobulinemia, X-Linked 71 0.034
524
P CRD119 Cardiac Arrest 71 0.034
525
BRN024 Bronchitis 70 0.034
526
BHC003 Behcet Syndrome 70 0.034
527
CNN005 Connective Tissue Disease 68 0.034
528
P DRM053 Dermatitis, Atopic 68 0.034
529
GLN010 Glanzmann Thrombasthenia 66 0.034
530
OMN001 Omenn Syndrome 66 0.034
531
c INF071 Inflammatory Bowel Disease 1 66 0.034
532
MSM014 Mismatch Repair Cancer Syndrome 65 0.034
533
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.034
534
c GCH015 Gaucher Disease, Type I 65 0.034
535
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.034
536
OST017 Osteomyelitis 65 0.034
537
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.034
538
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.034
539
CLR108 Colorectal Adenoma 64 0.034
540
MYX005 Myxoid Liposarcoma 64 0.034
541
c MCP001 Mucopolysaccharidosis Iii 64 0.034
542
LPD008 Lipid Metabolism Disorder 64 0.034
543
DRM006 Dermatitis 63 0.034
544
P GCH001 Gaucher's Disease 63 0.034
545
P MST009 Mastocytosis 62 0.034
546
P EPD009 Epidermolysis Bullosa Dystrophica 62 0.034
547
P LPS002 Liposarcoma 62 0.034
548
RFS006 Refsum Disease, Classic 62 0.034
549
P SNS001 Sensorineural Hearing Loss 62 0.034
550
RHB001 Rhabdoid Cancer 62 0.034
551
INT066 Interstitial Lung Disease 61 0.034
552
P URT039 Urticaria 61 0.034
553
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.034
554
c LCL006 Localized Scleroderma 61 0.034
555
c MCP052 Mucopolysaccharidosis, Type Vi 61 0.034
556
P TXP001 Toxoplasmosis 61 0.034
557
P ADL010 Adult Respiratory Distress Syndrome 61 0.034
558
P CND004 Candidiasis 61 0.034
559
c MCP049 Mucopolysaccharidosis, Type Vii 60 0.034
560
ADN018 Adenoma 60 0.034
561
P OPT006 Optic Nerve Disease 59 0.034
562
NRN004 Neuroendocrine Tumor 59 0.034
563
P MCR256 Microphthalmia, Syndromic 9 59 0.034
564
CNS004 Constipation 59 0.034
565
P THR005 Thrombotic Thrombocytopenic Purpura 59 0.034
566
P FCS002 Fucosidosis 58 0.034
567
P HYP726 Hypercalcemia, Infantile, 1 58 0.034
568
HPT022 Hepatoblastoma 58 0.034
569
LGS001 Legius Syndrome 57 0.034
570
c PRX059 Peroxisome Biogenesis Disorder 1a 57 0.034
571
P SJG008 Sjogren Syndrome 57 0.034
572
P MTC069 Mitochondrial Disorders 57 0.034
573
APH002 Aphasia 56 0.034
574
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.034
575
CRH005 Crohn's Colitis 56 0.034
576
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.034
577
P ZLL001 Zellweger Syndrome 56 0.034
578
GLS001 Gliosarcoma 56 0.034
579
SNS003 Sensory Peripheral Neuropathy 56 0.034
580
P PLM034 Pulmonary Emphysema 55 0.034
581
ORP003 Oropharynx Cancer 55 0.034
582
ASP002 Aspartylglucosaminuria 55 0.034
583
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 55 0.034
584
P SML001 Small Cell Carcinoma 55 0.034
585
P INS002 in Situ Carcinoma 55 0.034
586
VSC044 Visceral Myopathy 54 0.034
587
P RCT021 Rectum Cancer 54 0.034
588
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.034
589
P MYS005 Myositis 54 0.034
590
c RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.034
591
P CHL066 Cholangitis 53 0.034
592
EPT010 Epithelial-Myoepithelial Carcinoma 53 0.034
593
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.034
594
P PLY017 Polyarteritis Nodosa 52 0.034
595
P EMB005 Embryonal Rhabdomyosarcoma 52 0.034
596
P CNT005 Central Nervous System Lymphoma 52 0.034
597
RVS001 Revesz Syndrome 52 0.034
598
SRS001 Serous Cystadenocarcinoma 51 0.034
599
MCR088 Microscopic Polyangiitis 51 0.034
600
CYS014 Cystadenocarcinoma 51 0.034
601
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.034
602
P ANL018 Analbuminemia 51 0.034
603
CLR003 Clear Cell Adenocarcinoma 51 0.034
604
HYP080 Hypogonadism 51 0.034
605
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 0.034
606
GLM004 Gliomatosis Cerebri 50 0.034
607
ACR041 Acromelic Frontonasal Dysostosis 50 0.034
608
c THR071 Thrombocytopenia 1 50 0.034
609
DSM007 Desmoplastic Small Round Cell Tumor 50 0.034
610
PLR008 Pleurisy 50 0.034
611
c INF145 Infantile Liver Failure Syndrome 1 50 0.034
612
ATS010 Autosomal Recessive Disease 49 0.034
613
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 49 0.034
614
MLL001 Molluscum Contagiosum 49 0.034
615
BWN001 Bowen-Conradi Syndrome 49 0.034
616
TST015 Testicular Disease 49 0.034
617
c INV001 Invasive Aspergillosis 48 0.034
618
EWN002 Ewing's Family of Tumors 48 0.034
619
CHR001 Churg-Strauss Syndrome 48 0.034
620
HYR002 Hoyeraal Hreidarsson Syndrome 48 0.034
621
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.034
622
SPH010 Sphingolipidosis 47 0.034
623
P GND004 Gonadal Dysgenesis 47 0.034
624
ESN020 Eosinophilic Granulomatosis with Polyangiitis 47 0.034
625
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.034
626
c CHR283 Chronic Inflammatory Demyelinating Polyneuropathy 47 0.034
627
GRM005 Germ Cell Cancer 47 0.034
628
ACT029 Acute Interstitial Pneumonia 46 0.034
629
MCR225 Macrophage Activation Syndrome 46 0.034
630
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.034
631
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 45 0.034
632
PRX001 Peroxisomal Disease 45 0.034
633
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.034
634
c RHB023 Rhabdomyosarcoma, Embryonal, 1 44 0.034
635
VLV044 Vulvar Intraepithelial Neoplasia 44 0.034
636
MTC004 Mitochondrial Encephalomyopathy 44 0.034
637
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.034
638
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 44 0.034
639
DFF037 Diffuse Intrinsic Pontine Glioma 43 0.034
640
APP009 Appendix Adenocarcinoma 43 0.034
641
c ZLL011 Zellweger Spectrum Disorder 43 0.034
642
c MCL066 Macular Dystrophy, Vitelliform, 2 43 0.034
643
c HMG001 Hemoglobin C Disease 43 0.034
644
P VTL001 Vitelliform Macular Dystrophy 43 0.034
645
c 46X002 46 Xx Gonadal Dysgenesis 43 0.034
646
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 42 0.034
647
THR035 Thrombasthenia 42 0.034
648
P GLM044 Glomerular Disease 42 0.034
649
PPL001 Papillary Adenoma 42 0.034
650
c CNG413 Congenital Short Bowel Syndrome 42 0.034
651
RDN001 Reading Disorder 42 0.034
652
CRV045 Cervical Intraepithelial Neoplasia 41 0.034
653
DND018 Dendritic Cell Tumor 41 0.034
654
c HYP829 Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive 40 0.034
655
INT319 Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked 40 0.034
656
HYP064 Hypogonadotropism 40 0.034
657
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.034
658
VLV036 Vulvar Disease 38 0.034
659
P SML002 Small Cell Sarcoma 38 0.034
660
ENT008 Enteropathy-Associated T-Cell Lymphoma 38 0.034
661
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.034
662
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 38 0.034
663
LNG013 Lung Lymphoma 38 0.034
664
BLS007 Blastic Plasmacytoid Dendritic Cell 37 0.034
665
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 37 0.034
666
P OVR075 Ovarian Dysgenesis 1 37 0.034
667
OVR105 Ovarian Serous Carcinoma 37 0.034
668
CRT012 Cortical Blindness 37 0.034
669
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.034
670
c PRM304 Primary Hemophagocytic Lymphohistiocytosis 36 0.034
671
RFR013 Refractory Celiac Disease 35 0.034
672
HDG005 Hodgkin's Lymphoma, Mixed Cellularity 35 0.034
673
P INH011 Inherited Bone Marrow Failure Syndromes 34 0.034
674
HRS011 Horseshoe Kidney 34 0.034
675
BST007 Best Vitelliform Macular Dystrophy 34 0.034
676
P INV008 Invasive Pneumococcal Disease, Recurrent Isolated, 1 33 0.034
677
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 30 0.034
678
P SCK034 Sickle Beta Thalassemia 29 0.034
679
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 27 0.034
680
BNM005 Bone Marrow Necrosis 26 0.034
681
ALL012 Allergic Angiitis 25 0.034
682
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.034
683
PRX034 Peroxisome Disorders 22 0.034
684
DCK002 Dock8 Immunodeficiency Syndrome 20 0.034
685
OVR103 Ovarian Endometrial Cancer 17 0.034
686
P OST002 Osteoporosis 79 0.024
687
P MDL005 Medulloblastoma 78 0.024
688
P NRF023 Neurofibromatosis, Type Ii 77 0.024
689
c THR092 Thrombophilia Due to Thrombin Defect 74 0.024
690
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.024
691
PLM001 Pulmonary Tuberculosis 72 0.024
692
OTT002 Otitis Media 71 0.024
693
P HYP086 Hypothyroidism 70 0.024
694
c HMP029 Hemophilia a 69 0.024
695
PNC129 Pancreatic Adenocarcinoma 69 0.024
696
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.024
697
c CHR684 Chronic Kidney Disease 68 0.024
698
P MYS003 Myasthenia Gravis 68 0.024
699
c JVN010 Juvenile Rheumatoid Arthritis 67 0.024
700
P CNJ013 Conjunctivitis 67 0.024
701
GST040 Gastric Adenocarcinoma 67 0.024
702
P DBT009 Diabetes Mellitus 66 0.024
703
SVR097 Severe Cutaneous Adverse Reaction 66 0.024
704
INC002 Inclusion Body Myositis 66 0.024
705
c FNC043 Fanconi Anemia, Complementation Group E 64 0.024
706
P TST021 Testicular Germ Cell Tumor 63 0.024
707
c ATM011 Autoimmune Hepatitis 63 0.024
708
c SYS004 Systemic Mastocytosis 63 0.024
709
P FCL005 Focal Segmental Glomerulosclerosis 63 0.024
710
P ESP024 Esophagitis 62 0.024
711
BRC012 Brucellosis 62 0.024
712
P DRM010 Dermatomyositis 62 0.024
713
THY029 Thyroid Carcinoma 62 0.024
714
P ART023 Arthropathy 61 0.024
715
MSL001 Measles 61 0.024
716
TKY002 Takayasu Arteritis 61 0.024
717
P CRD132 Cardiac Conduction Defect 61 0.024
718
BND020 Bone Disease 60 0.024
719
FBR086 Fibrolamellar Carcinoma 60 0.024
720
BRN002 Bronchiolitis 60 0.024
721
THY122 Thyroid Gland Cancer 59 0.024
722
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 59 0.024
723
P HDC001 Headache 59 0.024
724
c GCH016 Gaucher Disease, Type Ii 59 0.024
725
P UVT001 Uveitis 58 0.024
726
P OCL002 Oculocutaneous Albinism 58 0.024
727
LYM021 Lymphadenitis 58 0.024
728
P HMP007 Hemophilia 58 0.024
729
DSS009 Disseminated Intravascular Coagulation 58 0.024
730
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.024
731
P PLY041 Polymyositis 57 0.024
732
GLL018 Gallbladder Cancer 57 0.024
733
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.024
734
ERY003 Erythema Multiforme 57 0.024
735
P GLL022 Guillain-Barre Syndrome 56 0.024
736
c BCT007 Bacterial Meningitis 56 0.024
737
c VRL010 Viral Hepatitis 56 0.024
738
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.024
739
WST005 West Nile Virus 56 0.024
740
GRN051 Granulomatous Disease, Chronic, X-Linked 55 0.024
741
BRN012 Bronchiolitis Obliterans 55 0.024
742
HYP005 Hypokalemia 55 0.024
743
P OPT009 Optic Neuritis 55 0.024
744
HMP005 Hemiplegia 55 0.024
745
MMB001 Membranoproliferative Glomerulonephritis 54 0.024
746
FCT001 Factor Viii Deficiency 54 0.024
747
DMY004 Demyelinating Disease 54 0.024
748
THY030 Thyroid Gland Disease 53 0.024
749
PGM001 Pigmented Villonodular Synovitis 52 0.024
750
LYS002 Lysosomal Storage Disease 52 0.024
751
NRT004 Neuritis 52 0.024
752
P AST007 Astrocytoma 52 0.024
753
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.024
754
CRY005 Cryptococcosis 51 0.024
755
DYS014 Dyspepsia 51 0.024
756
IMM064 Immunodeficiency, Common Variable, 10 51 0.024
757
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 50 0.024
758
P END047 Endophthalmitis 50 0.024
759
P ESN008 Eosinophilic Pneumonia 50 0.024
760
RYN005 Raynaud Phenomenon 50 0.024
761
P IDP024 Idiopathic Inflammatory Myopathy 49 0.024
762
EPD006 Epidermolysis Bullosa Acquisita 49 0.024
763
TST014 Testicular Cancer 49 0.024
764
c BCT013 Bacterial Pneumonia 49 0.024
765
GST027 Gastric Lymphoma 49 0.024
766
CYT005 Cytomegalovirus Retinitis 49 0.024
767
c CNG027 Congenital Hemolytic Anemia 48 0.024
768
SCT005 Scott Syndrome 48 0.024
769
c ANT034 Anterior Uveitis 48 0.024
770
ALB002 Albinism 48 0.024
771
HYP017 Hypophosphatemia 48 0.024
772
BRN014 Bronchopneumonia 47 0.024
773
HYP025 Hyperphosphatemia 47 0.024
774
c ACQ014 Acquired Hemophilia 47 0.024
775
MLR002 Miliary Tuberculosis 47 0.024
776
RTN023 Retinitis 46 0.024
777
NRR001 Neuroretinitis 46 0.024
778
EXT033 Extrapulmonary Tuberculosis 46 0.024
779
PRS063 Paresthesia 46 0.024
780
NWC001 Newcastle Disease 45 0.024
781
CYN002 Cyanosis, Transient Neonatal 45 0.024
782
IDP033 Idiopathic Edema 44 0.024
783
NCR004 Nocardiosis 44 0.024
784
BLR013 Biliary Tract Cancer 44 0.024
785
EVN001 Evans' Syndrome 44 0.024
786
BCL002 B Cell Deficiency 44 0.024
787
BCT021 Bacterial Sepsis 44 0.024
788
CNN010 Connective Tissue Benign Neoplasm 44 0.024
789
c GMM003 Gamma Heavy Chain Disease 43 0.024
790
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.024
791
P PRL003 Proliferative Glomerulonephritis 43 0.024
792
CRS001 Crescentic Glomerulonephritis 42 0.024
793
EMB007 Embryonal Sarcoma 42 0.024
794
c VRL005 Viral Pneumonia 42 0.024
795
GND003 Gonadal Disease 41 0.024
796
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.024
797
P TST026 Testicular Germ Cell Cancer 40 0.024
798
MNT303 Mental Retardation, X-Linked, Syndromic, Cabezas Type 40 0.024
799
TTT001 Tatton-Brown-Rahman Syndrome 39 0.024
800
c OST126 Osteopetrosis, Autosomal Recessive 1 39 0.024
801
CRB004 Cerebral Artery Occlusion 38 0.024
802
SPS057 Spasticity 38 0.024
803
c ATS384 Autosomal Dominant Non-Syndromic Intellectual Disability 2 38 0.024
804
UVL010 Uveal Disease 37 0.024
805
INT221 Intravascular Large B-Cell Lymphoma 36 0.024
806
c TYP024 Type Ii Mixed Cryoglobulinemia 36 0.024
807
c ATS282 Autosomal Recessive Malignant Osteopetrosis 36 0.024
808
c PRM301 Primary Cutaneous T-Cell Lymphoma 35 0.024
809
MDS019 Mediastinal Malignant Lymphoma 35 0.024
810
EPD005 Epidural Abscess 35 0.024
811
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 35 0.024
812
ACT011 Acute Contagious Conjunctivitis 35 0.024
813
LST003 Listeria Meningitis 34 0.024
814
ERY002 Erythema Infectiosum 34 0.024
815
BRN005 Brain Glioblastoma Multiforme 34 0.024
816
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.024
817
CMP001 Composite Lymphoma 33 0.024
818
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 33 0.024
819
LGH019 Light Fixation Seizure Syndrome 31 0.024
820
ENG004 Engraftment Syndrome 30 0.024
821
c TST046 Testicular Germ Cell Tumor 1 30 0.024
822
EMB015 Embryonal Tumor with Multilayered Rosettes 29 0.024
823
ERY066 Erythema Multiforme Major 29 0.024
824
P OVR096 Overlap Myositis 28 0.024
825
c THR102 Thrombocytopenia 5 28 0.024
826
PMP008 Pemphigus Vegetans 27 0.024
827
c ACQ016 Acquired Pure Red Cell Aplasia 27 0.024
828
ATY022 Atypical Coarctation of Aorta 26 0.024
829
SYN092 Syndromic X-Linked Intellectual Disability Cabezas Type 23 0.024
830
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 19 0.024
831
P RFR014 Refractory Anemia with Excess Blasts Type 2 19 0.024
832
PRM133 Primary Pulmonary Lymphoma 18 0.024
833
c RFR015 Refractory Anemia with Excess Blasts Type 1 16 0.024
Content
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