Search results for Fludarabine

824 hits were found for Fludarabine

# Family MCID Name MIFTS Score
1
P LKM002 Leukemia 68 0.782
2
P LKM071 Leukemia, Chronic Lymphocytic 79 0.765
3
P GRF003 Graft-Versus-Host Disease 72 0.667
4
P LYM118 Lymphoma 68 0.633
5
P MYL006 Myeloid Leukemia 60 0.616
6
c LKM061 Leukemia, Acute Myeloid 84 0.612
7
LYM019 Lymphosarcoma 46 0.585
8
MYL009 Myelodysplastic Syndrome 70 0.559
9
P LKM062 Leukemia, Acute Lymphoblastic 69 0.453
10
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.447
11
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.438
12
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.434
13
c CHR064 Chronic Monocytic Leukemia 33 0.433
14
LYM133 Lymphoma, Hodgkin, Classic 69 0.426
15
c ACT135 Acute Graft Versus Host Disease 52 0.419
16
LYM040 Lymphoblastic Lymphoma 54 0.393
17
c LKM063 Leukemia, Chronic Myeloid 72 0.393
18
HMT002 Hematologic Cancer 62 0.392
19
DFC004 Deficiency Anemia 70 0.384
20
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.384
21
c CHR417 Chronic Graft Versus Host Disease 57 0.376
22
MYL069 Myeloma, Multiple 85 0.374
23
P FLL037 Follicular Lymphoma 67 0.371
24
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.370
25
PLS009 Plasma Cell Neoplasm 51 0.363
26
P BCL017 B-Cell Lymphoma 58 0.359
27
MNT001 Mantle Cell Lymphoma 69 0.340
28
c ACT073 Acute Leukemia 58 0.340
29
c PRM038 Primary Agammaglobulinemia 44 0.321
30
HML018 Homologous Wasting Disease 22 0.310
31
P CNR004 Cone-Rod Dystrophy 2 73 0.305
32
c FLL041 Follicular Lymphoma 1 49 0.301
33
P NTR004 Neutropenia 63 0.297
34
MYL031 Myeloproliferative Neoplasm 66 0.294
35
MCR004 Macroglobulinemia 49 0.294
36
BNM001 Bone Marrow Cancer 43 0.288
37
P APL001 Aplastic Anemia 74 0.283
38
P CHR285 Chronic Myelomonocytic Leukemia 60 0.262
39
ADL002 Adult Syndrome 70 0.261
41
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.255
42
MRG003 Marginal Zone B-Cell Lymphoma 52 0.254
43
LYM012 Lymphoplasmacytic Lymphoma 47 0.253
44
WLD007 Waldenstroem's Macroglobulinemia 61 0.252
45
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.252
46
P TRN020 Turner Syndrome 67 0.250
47
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.250
48
BRK010 Burkitt Lymphoma 67 0.247
49
MYL005 Myelofibrosis 70 0.244
50
RFR010 Refractory Anemia 48 0.239
51
P MLN008 Melanoma 69 0.234
52
SKN019 Skin Melanoma 68 0.234
53
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.234
54
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.221
55
c RHB024 Rhabdomyosarcoma 2 67 0.220
56
PLS025 Plasmablastic Lymphoma 47 0.216
57
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.214
58
PRL017 Prolymphocytic Leukemia 47 0.213
59
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.209
60
IMM167 Immune Deficiency Disease 78 0.206
61
CHL149 Childhood Acute Myeloid Leukemia 44 0.203
62
MYC006 Mycosis Fungoides 66 0.193
63
P SRC025 Sarcoidosis 1 70 0.192
64
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.192
65
HDG004 Hodgkin's Granuloma 23 0.192
66
HDG006 Hodgkin's Paragranuloma 22 0.192
67
c FNC027 Fanconi Anemia, Complementation Group a 81 0.190
68
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.190
69
c LKM005 Leukemia, T-Cell, Chronic 34 0.190
70
P LYM033 Lymphoproliferative Syndrome 59 0.189
71
DFF005 Diffuse Large B-Cell Lymphoma 55 0.186
72
SPL004 Splenic Marginal Zone Lymphoma 51 0.184
73
P THR014 Thrombocytopenia 67 0.183
74
c CHR418 Chronic Leukemia 49 0.181
75
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.181
76
P ADL017 Adult T-Cell Leukemia 56 0.180
77
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.178
78
FNG017 Fungal Infectious Disease 53 0.177
79
RTC005 Reticulosarcoma 47 0.175
80
CYT002 Cytokine Deficiency 42 0.173
81
SZR001 Sezary's Disease 60 0.172
82
ATY042 Atypical Chronic Myeloid Leukemia 49 0.170
83
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.168
84
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.165
85
FCT007 Factor Vii Deficiency 67 0.163
86
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.163
87
MCS002 Mucositis 56 0.161
88
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.161
89
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.161
90
PLY001 Polycythemia Vera 69 0.158
91
P PLY018 Polycythemia 56 0.158
92
c PRM012 Primary Polycythemia 50 0.158
93
DWN001 Down Syndrome 70 0.154
94
LYM027 Lymphopenia 58 0.154
95
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.154
96
LYM051 Lymphomatoid Granulomatosis 45 0.154
97
HRY003 Hairy Cell Leukemia 55 0.151
98
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.151
99
P CTN015 Cutaneous T Cell Lymphoma 49 0.151
100
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.151
101
HPT046 Hepatic Veno-Occlusive Disease 56 0.149
102
P SCK005 Sickle Cell Disease 50 0.149
103
CLL014 Cll/sll 45 0.149
104
P FNC004 Fanconi Syndrome 50 0.145
105
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.143
106
P ESS003 Essential Thrombocythemia 68 0.139
107
P KDN017 Kidney Cancer 60 0.139
108
PLS016 Plasma Cell Leukemia 53 0.139
109
c THR090 Thrombocythemia 1 49 0.139
110
P HML002 Hemolytic Anemia 63 0.137
111
48X005 48,xyyy 39 0.137
112
SCK003 Sickle Cell Anemia 74 0.135
113
PNC001 Pancytopenia 54 0.135
114
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.133
115
P OVR042 Ovarian Cancer 88 0.130
116
ALL026 Allergic Hypersensitivity Disease 62 0.130
117
P THL005 Thalassemia 60 0.130
118
PRP036 Peripheral T-Cell Lymphoma 53 0.130
119
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.130
120
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.128
121
GRN017 Granulocytopenia 44 0.128
122
SPR126 Superior Semicircular Canal Dehiscence 40 0.128
123
c HMG029 Hemoglobin Se Disease 39 0.128
124
MXD050 Mixed Phenotype Acute Leukemia 43 0.126
125
SRC014 Sarcoma 65 0.124
126
MGK001 Megakaryocytic Leukemia 64 0.124
127
P ANP001 Anaplastic Large Cell Lymphoma 58 0.124
128
CYS036 Cystinosis, Nephropathic 51 0.124
129
P FNC034 Fanconi Renotubular Syndrome 2 40 0.124
130
c CHR682 Chronic Bilirubin Encephalopathy 39 0.124
131
ERY051 Erythroleukemia, Familial 56 0.121
132
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.121
133
SPN035 Spindle Cell Sarcoma 53 0.119
134
LRG008 Large Granular Lymphocyte Leukemia 41 0.119
135
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.117
136
c ANM038 Anemia, Autoimmune Hemolytic 62 0.117
137
SFT003 Soft Tissue Sarcoma 56 0.117
138
HMG005 Hemoglobinopathy 56 0.117
139
ATX019 Ataxia with Vitamin E Deficiency 42 0.117
140
P MLG074 Malignant Mesenchymoma 40 0.117
141
c OVR114 Ovarian Cancer 1 38 0.117
142
c ALP101 Alpha-Thalassemia 62 0.114
143
CHR286 Chronic Neutrophilic Leukemia 42 0.114
144
SVR004 Severe Combined Immunodeficiency 73 0.112
145
VRL011 Viral Infectious Disease 61 0.112
146
P EXN002 Exanthem 57 0.112
147
SKN013 Skin Benign Neoplasm 51 0.112
148
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.112
149
P CHR012 Chronic Granulomatous Disease 67 0.106
150
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.106
151
HMG002 Hemoglobinuria 50 0.106
152
INT054 Intraocular Lymphoma 48 0.106
153
CHR563 Chronic Eosinophilic Leukemia 48 0.106
154
RCH001 Richter's Syndrome 45 0.106
155
LTH001 Lethal Midline Granuloma 44 0.106
156
P SKN015 Skin Carcinoma 66 0.104
157
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.104
158
P NRB001 Neuroblastoma 72 0.101
159
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.101
160
P PNM007 Pneumonia 68 0.101
161
P CYS018 Cystitis 59 0.101
162
47X002 47,xyy 49 0.101
163
ACT098 Acute Erythroid Leukemia 48 0.101
164
c LKM070 Leukemia, Acute Monocytic 57 0.098
165
P DRR001 Diarrhea 55 0.098
166
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.098
167
SPL018 Splenomegaly 48 0.098
168
P LNG032 Lung Cancer 98 0.095
169
P HPT021 Hepatitis 67 0.095
170
P DYS007 Dyskeratosis Congenita 67 0.095
171
SQM006 Squamous Cell Carcinoma 60 0.095
172
c HPT016 Hepatitis B 59 0.095
173
P SZR006 Seizure Disorder 56 0.095
174
P BRS047 Breast Cancer 97 0.092
175
c BTT014 Beta-Thalassemia 74 0.092
176
P DMN001 Diamond-Blackfan Anemia 69 0.092
177
HRP004 Herpes Zoster 60 0.092
178
PLS011 Plasmacytoma 56 0.092
179
P MNC007 Monocytic Leukemia 53 0.092
180
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.092
181
P KDN018 Kidney Disease 72 0.089
182
P HYP098 Hypereosinophilic Syndrome 67 0.089
183
c SML038 Small Cell Cancer of the Lung 65 0.089
184
ACT119 Acute Promyelocytic Leukemia 63 0.089
185
CMB003 Combined T Cell and B Cell Immunodeficiency 49 0.089
186
HMR023 Hemorrhagic Cystitis 45 0.089
187
RDC006 Red Cell Aplasia 43 0.089
188
CMB081 Combined Immunodeficiency, X-Linked 36 0.089
189
CHL079 Children's Interstitial Lung Disease 26 0.089
190
P CLR023 Colorectal Cancer 99 0.086
191
P PNC035 Pancreatic Cancer 84 0.086
192
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.086
193
CNG034 Congestive Heart Failure 69 0.086
194
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.086
195
P ALP008 Alopecia 54 0.086
196
PST046 Post-Transplant Lymphoproliferative Disease 53 0.086
197
P PRR002 Pure Red-Cell Aplasia 47 0.086
198
CHR178 Chromosomal Triplication 35 0.086
199
c ADL093 Adult Acute Monocytic Leukemia 20 0.086
200
ADR007 Adrenoleukodystrophy 75 0.082
201
P WSK001 Wiskott-Aldrich Syndrome 72 0.082
202
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.082
203
c DMN023 Diamond-Blackfan Anemia 1 53 0.082
204
ACT200 Acute Monoblastic Leukemia 52 0.082
205
c DRR009 Diarrhea 6 46 0.082
206
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.082
207
IMM136 Immune System Disease 45 0.082
208
TRP009 Triple X Syndrome 42 0.082
209
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.082
210
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.082
211
CLS052 Classic Hairy Cell Leukemia 27 0.082
212
P HPT023 Hepatocellular Carcinoma 100 0.079
213
c SYS001 Systemic Lupus Erythematosus 86 0.079
214
P GLM040 Glioma Susceptibility 1 81 0.079
215
HMN044 Human Immunodeficiency Virus Type 1 71 0.079
216
P AMY004 Amyloidosis 70 0.079
217
P ART022 Arthritis 69 0.079
218
P ADN016 Adenocarcinoma 64 0.079
219
ATM095 Autoimmune Disease 62 0.079
220
TXC002 Toxic Encephalopathy 53 0.079
221
THR004 Thrombocytosis 51 0.079
222
c ALM001 Al Amyloidosis 50 0.079
223
RFR002 Refractory Hairy Cell Leukemia 33 0.079
224
GLB015 Glioblastoma Multiforme 75 0.075
225
P LVR013 Liver Disease 68 0.075
226
P LPS004 Lupus Erythematosus 61 0.075
227
ACQ007 Acquired Immunodeficiency Syndrome 60 0.075
228
LNG108 Langerhans Cell Histiocytosis 58 0.075
229
HST010 Histiocytosis 48 0.075
230
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.075
231
CRV035 Cervical Cancer 76 0.071
232
P HRT032 Heart Disease 75 0.071
233
NTR005 Nutritional Deficiency Disease 62 0.071
234
P ENC018 Encephalopathy 61 0.071
235
CHC001 Chickenpox 60 0.071
236
DYS164 Dyskeratosis Congenita, X-Linked 60 0.071
237
P INF032 Infertility 57 0.071
238
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.071
239
P NRP001 Neuropathy 56 0.071
240
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.071
241
P MST002 Mast-Cell Leukemia 49 0.071
242
c TCL005 T-Cell Prolymphocytic Leukemia 49 0.071
243
P GST053 Gastric Cancer 83 0.067
244
P RHM011 Rheumatoid Arthritis 80 0.067
245
P RSP003 Respiratory Failure 74 0.067
246
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.067
247
P HRP006 Herpes Simplex 65 0.067
248
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.067
249
P PSR002 Psoriasis 62 0.067
250
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.067
251
PNM001 Pneumocystosis 59 0.067
252
PST011 Pustulosis of Palm and Sole 52 0.067
253
STM007 Stomatitis 50 0.067
254
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.067
255
c INH020 Inherited Metabolic Disorder 47 0.067
256
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.067
257
GLL048 Glial Tumor 45 0.067
258
CHR208 Chromosome 17p Deletion 23 0.067
259
ESP021 Esophageal Cancer 90 0.063
260
P OST001 Osteopetrosis 70 0.063
261
EWN003 Ewing Sarcoma 69 0.063
262
P SYS005 Systemic Scleroderma 68 0.063
263
CMM004 Common Variable Immunodeficiency 68 0.063
264
OST159 Osteogenic Sarcoma 66 0.063
265
CHD001 Chediak-Higashi Syndrome 66 0.063
266
c MCL013 Mucolipidosis Iv 66 0.063
267
P AGM001 Agammaglobulinemia 65 0.063
268
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.063
269
P RHB003 Rhabdomyosarcoma 63 0.063
270
P GLM045 Glioma 63 0.063
271
c SCL052 Scleroderma, Familial Progressive 61 0.063
272
LNG099 Lung Disease 60 0.063
273
c ACT071 Acute Kidney Failure 60 0.063
274
VSL002 Visual Epilepsy 59 0.063
275
SRC027 Sarcoma, Synovial 58 0.063
276
ISC004 Ischemia 58 0.063
277
P PRP019 Peripheral Nervous System Disease 58 0.063
278
P GLM007 Glomerulonephritis 57 0.063
279
IRN002 Iron Metabolism Disease 57 0.063
280
BLR008 Bilirubin Metabolic Disorder 57 0.063
281
CMR002 Coumarin Resistance 56 0.063
282
BCT022 Bacterial Infectious Disease 56 0.063
283
PPL022 Papilloma 54 0.063
284
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.063
285
SQM002 Squamous Cell Papilloma 46 0.063
286
P BCL005 B Cell Prolymphocytic Leukemia 39 0.063
287
OVR094 Ovarian Epithelial Cancer 38 0.063
288
c SYS043 Systemic Lupus Erythematosus 1 38 0.063
289
ATM052 Autoimmune Disease 1 37 0.063
290
LTT002 Letterer-Siwe Disease 33 0.063
291
FTL073 Fetal Anticonvulsant Syndrome 26 0.063
292
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.063
293
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.058
294
P BLD134 Bladder Cancer 79 0.058
295
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.058
296
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.058
297
CRB039 Cerebrovascular Disease 67 0.058
298
FLL027 Fallopian Tube Carcinoma 67 0.058
299
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.058
300
HRL003 Hurler Syndrome 65 0.058
301
c HPT001 Hepatitis C 62 0.058
302
P NPH012 Nephrotic Syndrome 60 0.058
303
P ALP009 Alopecia Areata 60 0.058
304
c SVR003 Severe Congenital Neutropenia 59 0.058
305
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.058
306
c MST023 Mesothelioma, Malignant 57 0.058
307
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.058
308
P PMP001 Pemphigus 54 0.058
309
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 54 0.058
310
c OST131 Osteopetrosis, Autosomal Dominant 2 53 0.058
311
NTR018 Neutrophilia, Hereditary 52 0.058
312
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 51 0.058
313
LNG031 Lung Benign Neoplasm 51 0.058
314
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.058
315
GST071 Gastrointestinal Carcinoma 47 0.058
316
P BNG032 Benign Mesothelioma 46 0.058
317
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.058
318
P PRM293 Primary Mediastinal B-Cell Lymphoma 43 0.058
319
49X006 49, Xxxxy Syndrome 41 0.058
320
DFF003 Diffuse Scleroderma 41 0.058
321
NDL024 Nodal Marginal Zone Lymphoma 38 0.058
322
ADR022 Adrenomyeloneuropathy 38 0.058
323
IND016 Indolent B-Cell Non-Hodgkin Lymphoma 34 0.058
324
RFR004 Refractory Hematologic Cancer 30 0.058
326
P PRS040 Prostate Cancer 97 0.053
327
P ATX030 Ataxia-Telangiectasia 82 0.053
328
STR067 Stroke, Ischemic 81 0.053
329
BRN028 Brain Cancer 74 0.053
330
CRH001 Crohn's Disease 74 0.053
331
P MLT020 Multiple Sclerosis 72 0.053
332
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.053
333
P INF038 Influenza 68 0.053
334
P NSP012 Nasopharyngeal Carcinoma 66 0.053
335
MRK001 Merkel Cell Carcinoma 65 0.053
336
c WLM013 Wilms Tumor 1 65 0.053
337
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.053
338
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.053
339
c ACT068 Acute Cystitis 63 0.053
340
TXC005 Toxic Shock Syndrome 62 0.053
341
c WLM018 Wilms Tumor 5 61 0.053
342
VGN017 Vaginal Cancer 60 0.053
343
P MLN069 Melanoma, Uveal 59 0.053
344
LST001 Listeriosis 56 0.053
345
P PLY019 Polyneuropathy 56 0.053
346
PRP030 Purpura 54 0.053
347
HMS001 Hemosiderosis 54 0.053
348
CLR030 Clear Cell Renal Cell Carcinoma 53 0.053
349
c PSR017 Psoriasis 2 53 0.053
350
c PSR023 Psoriasis 1 52 0.053
351
TLN003 Telangiectasis 52 0.053
352
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.053
353
OCL022 Ocular Melanoma 50 0.053
354
GST049 Gastrointestinal System Cancer 49 0.053
355
MYL003 Myeloid Sarcoma 49 0.053
356
c PSR032 Psoriasis 11 47 0.053
357
CHR492 Chromosome 13q14 Deletion Syndrome 46 0.053
358
TCL003 T Cell Deficiency 46 0.053
359
c MLG068 Malignant Glioma 46 0.053
360
EXT010 Extramedullary Plasmacytoma 45 0.053
361
MXD026 Mixed Glioma 45 0.053
362
CLD007 Cold Agglutinin Disease 45 0.053
363
P HYP073 Hypersensitivity Reaction Type Iv Disease 44 0.053
364
PRN049 Paraneoplastic Pemphigus 42 0.053
365
c PSR028 Psoriasis 7 42 0.053
366
c PSR018 Psoriasis 13 41 0.053
367
P RRH023 Rare Hereditary Hemochromatosis 41 0.053
368
THR123 Thrombotic Microangiopathy 36 0.053
369
ACT118 Acute Non Lymphoblastic Leukemia 26 0.053
370
END057 Endometrial Cancer 74 0.048
371
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.048
372
P RTN024 Retinoblastoma 73 0.048
373
SCH036 Scheie Syndrome 72 0.048
374
P ASP006 Aspergillosis 69 0.048
375
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.048
376
P PLM037 Pulmonary Hypertension 67 0.048
377
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 0.048
378
P MNN013 Meningitis 66 0.048
379
DGR001 Digeorge Syndrome 64 0.048
380
RBR001 Roberts Syndrome 64 0.048
381
IMM174 Immunodeficiency with Hyper-Igm, Type 1 63 0.048
382
P VSC011 Vasculitis 62 0.048
383
CRC021 Carcinosarcoma 62 0.048
384
PSR001 Psoriatic Arthritis 61 0.048
385
DPH001 Diphtheria 60 0.048
386
P CTR002 Cataract 60 0.048
387
STT001 Status Epilepticus 60 0.048
388
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.048
389
ANS011 Anus Cancer 56 0.048
390
VLC001 Velocardiofacial Syndrome 54 0.048
391
P EPD016 Epidermolysis Bullosa 53 0.048
392
c FML008 Familial Retinoblastoma 53 0.048
393
HYP014 Hyperuricemia 52 0.048
394
JCB001 Jacobsen Syndrome 52 0.048
395
END086 End Stage Renal Disease 51 0.048
396
ACT017 Acute Chest Syndrome 51 0.048
397
CHL061 Childhood Leukemia 48 0.048
398
CRY004 Cryoglobulinemia 48 0.048
399
P LYM024 Lymphatic System Disease 48 0.048
400
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.048
401
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.048
402
CRB138 Core Binding Factor Acute Myeloid Leukemia 43 0.048
403
P AVS003 Avascular Necrosis 42 0.048
404
GST020 Gastric Antral Vascular Ectasia 41 0.048
405
LKP003 Leukoplakia 39 0.048
406
c WLM011 Wilms Tumor 6 37 0.048
407
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 36 0.048
408
ACT177 Acute Basophilic Leukemia 34 0.048
409
GRM010 Germ Cells Tumors 34 0.048
410
c PRS136 Prostate Cancer, Hereditary, 6 33 0.048
411
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.048
412
c PRS130 Prostate Cancer, Hereditary, 8 32 0.048
413
P PLY188 Polyendocrinopathy 32 0.048
414
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 30 0.048
415
ANS025 Anus Benign Neoplasm 30 0.048
416
P LNG064 Lung Cancer Susceptibility 3 78 0.041
417
c ATR087 Atrial Standstill 1 75 0.041
418
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.041
419
c MNN043 Meningioma, Familial 74 0.041
420
c SPN225 Spondyloarthropathy 1 73 0.041
421
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.041
422
P MYC007 Myocardial Infarction 70 0.041
423
P MTC003 Metachromatic Leukodystrophy 70 0.041
424
P KRB001 Krabbe Disease 69 0.041
425
MST024 Mastocytosis, Cutaneous 69 0.041
426
P MYC084 Mycobacterium Tuberculosis 1 68 0.041
427
CHL065 Cholangiocarcinoma 68 0.041
428
c BSL007 Basal Cell Carcinoma 68 0.041
429
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.041
430
c INF071 Inflammatory Bowel Disease 1 67 0.041
431
P SHW006 Shwachman-Diamond Syndrome 1 67 0.041
432
LNG039 Lung Squamous Cell Carcinoma 66 0.041
433
P NRV007 Nervous System Disease 66 0.041
434
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.041
435
P PLM036 Pulmonary Fibrosis 65 0.041
436
TTN003 Tetanus 65 0.041
437
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.041
438
P VSC007 Vascular Disease 63 0.041
439
c MLG084 Malignant Fibrous Histiocytoma 63 0.041
440
SKN016 Skin Disease 63 0.041
441
CLT003 Colitis 62 0.041
442
MNN042 Meningioma, Radiation-Induced 62 0.041
443
PNM010 Pneumothorax, Primary Spontaneous 60 0.041
444
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.041
445
IDP011 Idiopathic Interstitial Pneumonia 59 0.041
446
P LKD001 Leukodystrophy 59 0.041
447
VLV032 Vulva Cancer 59 0.041
448
GST045 Gastroenteritis 59 0.041
449
MCS006 Macs Syndrome 58 0.041
450
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.041
451
P BNC003 Bone Cancer 58 0.041
452
GLS018 Glass Syndrome 57 0.041
453
CYT008 Cytomegalovirus Infection 57 0.041
454
HYP266 Hypoxia 57 0.041
455
AYM001 Ayme-Gripp Syndrome 57 0.041
456
PNM008 Pneumothorax 56 0.041
457
c BSL024 Basal Cell Carcinoma 1 56 0.041
458
P CHN012 Chondrosarcoma 56 0.041
459
c ACT134 Acute Liver Failure 56 0.041
460
P PNL012 Penile Cancer 56 0.041
461
BRN004 Brain Edema 56 0.041
462
HPT022 Hepatoblastoma 56 0.041
463
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.041
464
HRL004 Hurler-Scheie Syndrome 55 0.041
465
SYN007 Synovitis 54 0.041
466
P INF037 Inflammatory Bowel Disease 54 0.041
467
AMN001 Amenorrhea 54 0.041
468
P TRM003 Tremor 54 0.041
469
CRH005 Crohn's Colitis 53 0.041
470
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.041
471
c CNG208 Congenital Disorder of Glycosylation, Type Iic 51 0.041
472
P SPP010 Suppressor of Tumorigenicity 3 51 0.041
473
OCL069 Ocular Motor Apraxia 51 0.041
474
INT079 Intrahepatic Cholangiocarcinoma 51 0.041
475
PNN001 Panniculitis 51 0.041
476
P MMB011 Membranous Nephropathy 50 0.041
477
SPN021 Spinal Meningioma 50 0.041
478
MTB004 Metabolic Acidosis 50 0.041
479
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.041
480
BNG036 Bone Giant Cell Tumor 49 0.041
481
CRY014 Cryptococcal Meningitis 48 0.041
482
ADN009 Adenosquamous Carcinoma 47 0.041
483
CD4003 Cd40 Ligand Deficiency 46 0.041
484
BNS007 Bone Sarcoma 45 0.041
485
INT253 Intestinal Benign Neoplasm 45 0.041
486
ESP027 Esophagus Squamous Cell Carcinoma 45 0.041
487
OVR112 Ovarian Germ Cell Cancer 45 0.041
488
c MYL058 Myeloproliferative Syndrome, Transient 44 0.041
489
P BNG095 Benign Giant Cell Tumor 44 0.041
490
P DMY001 Demyelinating Polyneuropathy 43 0.041
491
P PRT026 Parotitis 42 0.041
492
c MLG079 Malignant Pleural Mesothelioma 42 0.041
493
IMM078 Immunodeficiency 21 42 0.041
494
c PST022 Posterior Uveal Melanoma 42 0.041
495
SCR001 Secretory Meningioma 41 0.041
496
DND018 Dendritic Cell Tumor 40 0.041
497
c HMG001 Hemoglobin C Disease 40 0.041
498
ORL012 Oral Leukoplakia 39 0.041
499
BLS007 Blastic Plasmacytoid Dendritic Cell 38 0.041
500
MCP033 Mucopolysaccharidoses 38 0.041
501
LYM052 Lymphomatoid Papulosis 38 0.041
502
SYS071 Systemic Autoimmune Disease 37 0.041
503
PLC002 Plica Syndrome 36 0.041
504
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.041
505
RFR013 Refractory Celiac Disease 35 0.041
506
P HVY001 Heavy Chain Disease 34 0.041
507
P INH011 Inherited Bone Marrow Failure Syndromes 34 0.041
508
SML008 Small Intestine Lymphoma 33 0.041
509
MYC088 Mycobacterium Avium Complex Infections 29 0.041
510
c THR110 Thrombocytopenia 6 28 0.041
511
PGM030 Pigmentation Anomaly of the Skin 26 0.041
512
MLG164 Malignant Epithelial Tumor of Ovary 26 0.041
513
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.041
514
IND005 Indolent B Cell Lymphoma 20 0.041
515
c BSL027 Basal Cell Carcinoma 4 16 0.041
516
PFF001 Pfeiffer Syndrome 79 0.034
517
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.034
518
ANX010 Anxiety 73 0.034
519
AGM019 Agammaglobulinemia, X-Linked 71 0.034
520
PRP027 Peripheral Vascular Disease 71 0.034
521
BHC003 Behcet Syndrome 71 0.034
522
c GCH015 Gaucher Disease, Type I 70 0.034
523
BRN024 Bronchitis 68 0.034
524
CNN005 Connective Tissue Disease 68 0.034
525
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.034
526
P CRD119 Cardiac Arrest 67 0.034
527
OMN001 Omenn Syndrome 67 0.034
528
GLN010 Glanzmann Thrombasthenia 66 0.034
529
MYX005 Myxoid Liposarcoma 66 0.034
530
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.034
531
P DRM053 Dermatitis, Atopic 66 0.034
532
P LPS002 Liposarcoma 65 0.034
533
MSM014 Mismatch Repair Cancer Syndrome 65 0.034
534
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.034
535
P ADL010 Adult Respiratory Distress Syndrome 65 0.034
536
P MST009 Mastocytosis 64 0.034
537
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.034
538
CLR108 Colorectal Adenoma 64 0.034
539
RFS006 Refsum Disease, Classic 64 0.034
540
OST017 Osteomyelitis 64 0.034
541
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.034
542
P GCH001 Gaucher's Disease 63 0.034
543
P LMY004 Leiomyosarcoma 63 0.034
544
RHB001 Rhabdoid Cancer 63 0.034
545
BLD131 Bladder Urothelial Carcinoma 62 0.034
546
ASP002 Aspartylglucosaminuria 62 0.034
547
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.034
548
DRM006 Dermatitis 61 0.034
549
CHR001 Churg-Strauss Syndrome 61 0.034
550
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.034
551
FCS002 Fucosidosis 61 0.034
552
P SJG008 Sjogren Syndrome 61 0.034
553
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.034
554
P TXP001 Toxoplasmosis 60 0.034
555
INT066 Interstitial Lung Disease 60 0.034
556
P MCR010 Microcephaly 59 0.034
557
LGS001 Legius Syndrome 59 0.034
558
ADN018 Adenoma 59 0.034
559
P PLY017 Polyarteritis Nodosa 58 0.034
560
P HYP726 Hypercalcemia, Infantile, 1 58 0.034
561
P URT039 Urticaria 58 0.034
562
CNS004 Constipation 58 0.034
563
P CND004 Candidiasis 58 0.034
564
P GLL018 Gallbladder Cancer 57 0.034
565
P ZLL001 Zellweger Syndrome 57 0.034
566
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.034
567
APH002 Aphasia 57 0.034
568
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 57 0.034
569
P MYS005 Myositis 56 0.034
570
TRN018 Transitional Cell Carcinoma 56 0.034
571
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.034
572
c MCR256 Microphthalmia, Syndromic 9 56 0.034
573
ORP003 Oropharynx Cancer 55 0.034
574
NRN004 Neuroendocrine Tumor 55 0.034
575
P PLM034 Pulmonary Emphysema 55 0.034
576
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.034
577
GLS001 Gliosarcoma 54 0.034
578
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.034
579
ANL018 Analbuminemia 54 0.034
580
RVS001 Revesz Syndrome 54 0.034
581
SNS003 Sensory Peripheral Neuropathy 54 0.034
582
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.034
583
P INS002 in Situ Carcinoma 53 0.034
584
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.034
585
P CNT005 Central Nervous System Lymphoma 53 0.034
586
P SHR001 Short Bowel Syndrome 53 0.034
587
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.034
588
ACR041 Acromelic Frontonasal Dysostosis 52 0.034
589
P SML001 Small Cell Carcinoma 52 0.034
590
GLM004 Gliomatosis Cerebri 52 0.034
591
P RCT021 Rectum Cancer 52 0.034
592
DSM007 Desmoplastic Small Round Cell Tumor 52 0.034
593
SRS001 Serous Cystadenocarcinoma 52 0.034
594
MCR088 Microscopic Polyangiitis 51 0.034
595
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.034
596
CYS014 Cystadenocarcinoma 51 0.034
597
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.034
598
P CHL066 Cholangitis 51 0.034
599
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 51 0.034
600
PLR008 Pleurisy 50 0.034
601
c INF145 Infantile Liver Failure Syndrome 1 50 0.034
602
MLL001 Molluscum Contagiosum 50 0.034
603
c THR071 Thrombocytopenia 1 50 0.034
604
CLR003 Clear Cell Adenocarcinoma 50 0.034
605
HYP080 Hypogonadism 50 0.034
606
INP001 Inappropriate Adh Syndrome 49 0.034
607
ACT029 Acute Interstitial Pneumonia 49 0.034
608
c INV001 Invasive Aspergillosis 49 0.034
609
WTH001 Withdrawal Disorder 48 0.034
610
ATS010 Autosomal Recessive Disease 48 0.034
611
PPL002 Papillary Carcinoma 47 0.034
612
SPH010 Sphingolipidosis 47 0.034
613
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 47 0.034
614
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.034
615
HYR002 Hoyeraal Hreidarsson Syndrome 46 0.034
616
VLV036 Vulvar Disease 46 0.034
617
PRX001 Peroxisomal Disease 46 0.034
618
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.034
619
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.034
620
c ZLL011 Zellweger Spectrum Disorder 45 0.034
621
APP009 Appendix Adenocarcinoma 44 0.034
622
MCR225 Macrophage Activation Syndrome 44 0.034
623
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 44 0.034
624
PPL001 Papillary Adenoma 44 0.034
625
VLV044 Vulvar Intraepithelial Neoplasia 44 0.034
626
CVD001 Covid-19 44 0.034
627
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.034
628
TST015 Testicular Disease 43 0.034
629
c MCL066 Macular Dystrophy, Vitelliform, 2 42 0.034
630
P VTL001 Vitelliform Macular Dystrophy 42 0.034
631
c HYP829 Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive 42 0.034
632
RDN001 Reading Disorder 40 0.034
633
THR035 Thrombasthenia 40 0.034
634
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.034
635
CRV045 Cervical Intraepithelial Neoplasia 39 0.034
636
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.034
637
SMT002 Smooth Muscle Tumor 38 0.034
638
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 38 0.034
639
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.034
640
CRT012 Cortical Blindness 37 0.034
641
GLM044 Glomerular Disease 37 0.034
642
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 37 0.034
643
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.034
644
LNG013 Lung Lymphoma 35 0.034
645
GRY001 Gray Zone Lymphoma 35 0.034
646
INV021 Invasive Pneumococcal Disease, Recurrent Isolated 35 0.034
647
SPN043 Spinal Cord Glioma 34 0.034
648
HRS011 Horseshoe Kidney 34 0.034
649
BST007 Best Vitelliform Macular Dystrophy 34 0.034
650
c PRM304 Primary Hemophagocytic Lymphohistiocytosis 33 0.034
651
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.034
652
HDG005 Hodgkin's Lymphoma, Mixed Cellularity 30 0.034
653
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.034
654
P SCK034 Sickle Beta Thalassemia 28 0.034
655
P SML002 Small Cell Sarcoma 27 0.034
656
BNM005 Bone Marrow Necrosis 25 0.034
657
HRP008 Herpes Simiae 25 0.034
658
ALL012 Allergic Angiitis 24 0.034
659
CHR176 Chromophil Renal Cell Carcinoma 23 0.034
660
OVR103 Ovarian Endometrial Cancer 23 0.034
661
DCK002 Dock8 Immunodeficiency Syndrome 19 0.034
662
c HYP595 Hypertension, Essential 84 0.024
663
c NRF023 Neurofibromatosis, Type Ii 80 0.024
664
P MDL005 Medulloblastoma 77 0.024
665
P OST002 Osteoporosis 74 0.024
666
P NJM001 Nijmegen Breakage Syndrome 74 0.024
667
c THR092 Thrombophilia Due to Thrombin Defect 73 0.024
668
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.024
669
OTT002 Otitis Media 72 0.024
670
GST040 Gastric Adenocarcinoma 70 0.024
671
c CHR684 Chronic Kidney Disease 70 0.024
672
PLM001 Pulmonary Tuberculosis 69 0.024
673
SVR097 Severe Cutaneous Adverse Reaction 69 0.024
674
P HYP086 Hypothyroidism 69 0.024
675
P MYS003 Myasthenia Gravis 68 0.024
676
PNC129 Pancreatic Adenocarcinoma 68 0.024
677
c HMP029 Hemophilia a 67 0.024
678
P CNJ013 Conjunctivitis 65 0.024
679
IRR002 Irritable Bowel Syndrome 65 0.024
680
c DBT099 Diabetes Mellitus, Type I 65 0.024
681
P DBT009 Diabetes Mellitus 64 0.024
682
c JVN010 Juvenile Rheumatoid Arthritis 64 0.024
683
BRC012 Brucellosis 64 0.024
684
c SYS004 Systemic Mastocytosis 63 0.024
685
c ATM011 Autoimmune Hepatitis 63 0.024
686
c FNC043 Fanconi Anemia, Complementation Group E 62 0.024
687
TKY002 Takayasu Arteritis 62 0.024
688
P ESP024 Esophagitis 62 0.024
689
P ART023 Arthropathy 62 0.024
690
MSL001 Measles 62 0.024
691
P DRM010 Dermatomyositis 61 0.024
692
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.024
693
FBR086 Fibrolamellar Carcinoma 61 0.024
694
P TST021 Testicular Germ Cell Tumor 60 0.024
695
c JVN061 Juvenile Arthritis 60 0.024
696
P OCL002 Oculocutaneous Albinism 60 0.024
697
P MYC008 Myocarditis 59 0.024
698
P BND020 Bone Disease 59 0.024
699
THY029 Thyroid Carcinoma 59 0.024
700
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.024
701
BRN002 Bronchiolitis 59 0.024
702
P GLL022 Guillain-Barre Syndrome 59 0.024
703
INC002 Inclusion Body Myositis 58 0.024
704
CRY005 Cryptococcosis 58 0.024
705
CRD132 Cardiac Conduction Defect 58 0.024
706
ERY003 Erythema Multiforme 58 0.024
707
c DWL002 Dowling-Degos Disease 1 58 0.024
708
P UVT001 Uveitis 57 0.024
709
P OPT009 Optic Neuritis 57 0.024
710
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.024
711
P PLY041 Polymyositis 57 0.024
712
P HDC001 Headache 57 0.024
713
DSS009 Disseminated Intravascular Coagulation 57 0.024
714
THY122 Thyroid Gland Cancer 57 0.024
715
LYM021 Lymphadenitis 57 0.024
716
P FCL005 Focal Segmental Glomerulosclerosis 57 0.024
717
PGM001 Pigmented Villonodular Synovitis 56 0.024
718
c INT072 Intestinal Pseudo-Obstruction 56 0.024
719
SPN041 Spinal Cord Disease 56 0.024
720
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.024
721
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.024
722
BRN012 Bronchiolitis Obliterans 55 0.024
723
HYP005 Hypokalemia 55 0.024
724
MMB001 Membranoproliferative Glomerulonephritis 55 0.024
725
c BCT007 Bacterial Meningitis 55 0.024
726
HMP005 Hemiplegia 55 0.024
727
NCR004 Nocardiosis 54 0.024
728
BRN014 Bronchopneumonia 54 0.024
729
WST005 West Nile Virus 54 0.024
730
P END047 Endophthalmitis 53 0.024
731
c GCH016 Gaucher Disease, Type Ii 53 0.024
732
IRD001 Iridocyclitis 53 0.024
733
DMY004 Demyelinating Disease 52 0.024
734
LYS002 Lysosomal Storage Disease 52 0.024
735
c VRL010 Viral Hepatitis 52 0.024
736
NRT004 Neuritis 52 0.024
737
THY030 Thyroid Gland Disease 52 0.024
738
HYP088 Hyper-Igd Syndrome 52 0.024
739
c VRL005 Viral Pneumonia 52 0.024
740
P HMP007 Hemophilia 51 0.024
741
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 51 0.024
742
FCT001 Factor Viii Deficiency 51 0.024
743
P AST007 Astrocytoma 51 0.024
744
P ESN008 Eosinophilic Pneumonia 50 0.024
745
CYT005 Cytomegalovirus Retinitis 50 0.024
746
c CNG027 Congenital Hemolytic Anemia 50 0.024
747
HYP017 Hypophosphatemia 50 0.024
748
c OST126 Osteopetrosis, Autosomal Recessive 1 49 0.024
749
SCT005 Scott Syndrome 49 0.024
750
EPD006 Epidermolysis Bullosa Acquisita 49 0.024
751
MLR002 Miliary Tuberculosis 49 0.024
752
c BCT013 Bacterial Pneumonia 48 0.024
753
EVN001 Evans' Syndrome 48 0.024
754
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.024
755
HYP025 Hyperphosphatemia 48 0.024
756
P ATT003 Attenuated Familial Adenomatous Polyposis 48 0.024
757
GRM005 Germ Cell Cancer 47 0.024
758
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.024
759
RYN005 Raynaud Phenomenon 47 0.024
760
RTN023 Retinitis 46 0.024
761
ALB002 Albinism 46 0.024
762
EXT033 Extrapulmonary Tuberculosis 46 0.024
763
CYN002 Cyanosis, Transient Neonatal 45 0.024
764
NWC001 Newcastle Disease 45 0.024
765
CRB004 Cerebral Artery Occlusion 45 0.024
766
c ACQ014 Acquired Hemophilia 45 0.024
767
SPS057 Spasticity 45 0.024
768
P END039 Endodermal Sinus Tumor 44 0.024
769
P PRL003 Proliferative Glomerulonephritis 44 0.024
770
GST027 Gastric Lymphoma 44 0.024
771
PRT035 Peritoneum Cancer 44 0.024
772
P EPN001 Ependymoblastoma 44 0.024
773
BCT021 Bacterial Sepsis 44 0.024
774
IDP033 Idiopathic Edema 44 0.024
775
P TST026 Testicular Germ Cell Cancer 43 0.024
776
MRG013 Mirage Syndrome 43 0.024
777
CRS001 Crescentic Glomerulonephritis 43 0.024
778
BCL002 B Cell Deficiency 43 0.024
779
BLR013 Biliary Tract Cancer 42 0.024
780
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.024
781
NRR001 Neuroretinitis 42 0.024
782
TTT001 Tatton-Brown-Rahman Syndrome 41 0.024
783
EMB007 Embryonal Sarcoma 41 0.024
784
PRS063 Paresthesia 41 0.024
785
MNT303 Mental Retardation, X-Linked, Syndromic, Cabezas Type 41 0.024
786
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.024
787
CNN010 Connective Tissue Benign Neoplasm 40 0.024
788
ACT011 Acute Contagious Conjunctivitis 40 0.024
789
CNT007 Central Nervous System Tuberculosis 39 0.024
790
TST018 Testicular Yolk Sac Tumor 39 0.024
791
c GMM003 Gamma Heavy Chain Disease 38 0.024
792
CMP001 Composite Lymphoma 37 0.024
793
c ATS282 Autosomal Recessive Malignant Osteopetrosis 37 0.024
794
INT221 Intravascular Large B-Cell Lymphoma 35 0.024
795
EPD005 Epidural Abscess 35 0.024
796
UVL010 Uveal Disease 35 0.024
797
c PRM301 Primary Cutaneous T-Cell Lymphoma 35 0.024
798
c TYP024 Type Ii Mixed Cryoglobulinemia 34 0.024
799
ATY022 Atypical Coarctation of Aorta 34 0.024
801
BRN005 Brain Glioblastoma Multiforme 34 0.024
802
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.024
803
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 33 0.024
804
ERY002 Erythema Infectiosum 33 0.024
805
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.024
806
WST010 West Nile Virus Infection 32 0.024
807
c ATS384 Autosomal Dominant Non-Syndromic Intellectual Disability 2 31 0.024
808
MDS019 Mediastinal Malignant Lymphoma 30 0.024
809
LGH019 Light Fixation Seizure Syndrome 30 0.024
810
ERY066 Erythema Multiforme Major 30 0.024
811
c THR102 Thrombocytopenia 5 30 0.024
812
ENG004 Engraftment Syndrome 30 0.024
813
c TST046 Testicular Germ Cell Tumor 1 29 0.024
814
LST003 Listeria Meningitis 29 0.024
815
SYN092 Syndromic X-Linked Intellectual Disability Cabezas Type 28 0.024
816
P OVR096 Overlap Myositis 27 0.024
817
PMP008 Pemphigus Vegetans 27 0.024
818
c ACQ016 Acquired Pure Red Cell Aplasia 27 0.024
820
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 21 0.024
821
P RFR014 Refractory Anemia with Excess Blasts Type 2 18 0.024
822
PRM133 Primary Pulmonary Lymphoma 18 0.024
823
c RFR015 Refractory Anemia with Excess Blasts Type 1 15 0.024
Content
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