Search results for Fludarabine

1036 hits were found for Fludarabine

# Family MCID Name MIFTS Score
1
P LKM071 Leukemia, Chronic Lymphocytic 74 27.554
2
P LKM002 Leukemia 66 24.941
3
c LKM061 Leukemia, Acute Myeloid 83 19.347
4
P MYL006 Myeloid Leukemia 60 18.312
5
P GRF003 Graft-Versus-Host Disease 71 17.556
6
MYL009 Myelodysplastic Syndrome 67 17.022
7
P LYM118 Lymphoma 69 16.848
8
DFC004 Deficiency Anemia 74 12.553
9
c ACT135 Acute Graft Versus Host Disease 51 12.252
10
P LKM062 Leukemia, Acute Lymphoblastic 69 12.085
11
LYM143 Lymphoma, Non-Hodgkin, Familial 79 11.490
12
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 11.479
13
LYM019 Lymphosarcoma 46 11.252
14
P FLL037 Follicular Lymphoma 73 10.948
15
LYM133 Lymphoma, Hodgkin, Classic 74 10.638
16
c LKM056 Leukemia, Chronic Lymphocytic 2 47 10.167
17
MYL069 Myeloma, Multiple 77 10.166
18
P NTR004 Neutropenia 62 9.787
19
c ACT073 Acute Leukemia 59 9.675
20
P APL001 Aplastic Anemia 73 9.564
21
MNT001 Mantle Cell Lymphoma 65 9.417
22
MCR004 Macroglobulinemia 48 9.297
23
P BCL017 B-Cell Lymphoma 57 9.038
24
c CHR064 Chronic Monocytic Leukemia 36 8.791
25
c LKM063 Leukemia, Chronic Myeloid 71 8.781
27
LYM040 Lymphoblastic Lymphoma 53 7.921
28
HMT002 Hematologic Cancer 61 7.663
29
MYL005 Myelofibrosis 70 7.462
30
PRL017 Prolymphocytic Leukemia 47 7.146
31
P TRN020 Turner Syndrome 67 7.091
32
PLS009 Plasma Cell Neoplasm 64 6.999
33
P CHR285 Chronic Myelomonocytic Leukemia 59 6.879
34
MYL031 Myeloproliferative Neoplasm 66 6.850
35
c FNC027 Fanconi Anemia, Complementation Group a 81 6.762
36
LYM012 Lymphoplasmacytic Lymphoma 50 6.739
37
ACT113 Acute Myeloblastic Leukemia with Maturation 46 6.635
38
P THR014 Thrombocytopenia 66 6.424
39
c CHR417 Chronic Graft Versus Host Disease 55 6.308
40
P ANR048 Aniridia 1 66 6.224
41
HML018 Homologous Wasting Disease 21 6.098
42
JVN004 Juvenile Myelomonocytic Leukemia 67 5.914
43
BNM001 Bone Marrow Cancer 45 5.791
44
RFR010 Refractory Anemia 49 5.680
45
P LYM033 Lymphoproliferative Syndrome 59 5.651
46
MCS002 Mucositis 55 5.502
47
WLD007 Waldenstroem's Macroglobulinemia 65 5.418
48
MYC006 Mycosis Fungoides 65 5.270
49
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 5.255
50
LYM027 Lymphopenia 56 5.237
51
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 5.194
52
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 5.122
53
ADL002 Adult Syndrome 69 5.004
54
P HML002 Hemolytic Anemia 62 4.955
55
HRY003 Hairy Cell Leukemia 61 4.954
56
BRK010 Burkitt Lymphoma 66 4.917
57
PNC001 Pancytopenia 52 4.879
58
IMM167 Immune Deficiency Disease 77 4.859
59
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.721
60
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 4.701
61
P SCK005 Sickle Cell Disease 56 4.690
62
c LKM005 Leukemia, T-Cell, Chronic 33 4.647
63
P CNR004 Cone-Rod Dystrophy 2 75 4.639
64
CLL014 Cll/sll 45 4.594
65
P CTN015 Cutaneous T Cell Lymphoma 48 4.582
66
P THL005 Thalassemia 56 4.518
67
SPL004 Splenic Marginal Zone Lymphoma 50 4.503
68
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 4.361
69
MRG003 Marginal Zone B-Cell Lymphoma 52 4.333
70
SVR004 Severe Combined Immunodeficiency 71 4.330
71
ANT039 Antisynthetase Syndrome 55 4.323
72
RCH001 Richter's Syndrome 44 4.315
73
P ADL017 Adult T-Cell Leukemia 54 4.276
74
c ANM038 Anemia, Autoimmune Hemolytic 63 4.276
75
AND005 Androgen Insensitivity Syndrome, Mild 21 4.229
76
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 4.224
77
FLL041 Follicular Lymphoma 1 44 4.189
78
P MLN008 Melanoma 75 4.172
79
DFF005 Diffuse Large B-Cell Lymphoma 55 4.154
80
AGN016 Aging 54 4.112
81
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 4.056
82
RHB024 Rhabdomyosarcoma 2 65 4.042
83
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 4.029
84
SKN019 Skin Melanoma 70 4.022
85
RNL114 Renal Cell Carcinoma, Nonpapillary 79 4.015
86
P SRC025 Sarcoidosis 1 70 3.998
87
PRP036 Peripheral T-Cell Lymphoma 52 3.969
88
c PRM038 Primary Agammaglobulinemia 47 3.968
89
HDG004 Hodgkin's Granuloma 22 3.893
90
HDG006 Hodgkin's Paragranuloma 21 3.893
91
P DMN001 Diamond-Blackfan Anemia 73 3.872
92
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 3.798
93
GRN017 Granulocytopenia 42 3.651
94
RTC005 Reticulosarcoma 47 3.603
95
CMB007 Combined Immunodeficiency 56 3.573
96
P CHR012 Chronic Granulomatous Disease 69 3.567
97
c LKM060 Leukemia, Acute Lymphoblastic 3 49 3.557
98
PLS025 Plasmablastic Lymphoma 56 3.554
99
P EXN002 Exanthem 58 3.400
100
FNG017 Fungal Infectious Disease 54 3.398
101
SZR001 Sezary's Disease 60 3.369
102
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 3.353
103
P HMP002 Hemophagocytic Lymphohistiocytosis 60 3.341
104
HMG002 Hemoglobinuria 50 3.295
105
P MXD050 Mixed Phenotype Acute Leukemia 45 3.285
106
CYS036 Cystinosis, Nephropathic 51 3.283
107
P PLY018 Polycythemia 56 3.254
108
48X005 48,xyyy 39 3.248
109
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 3.247
110
PLY001 Polycythemia Vera 69 3.233
111
P FNC004 Fanconi Syndrome 60 3.233
112
P ALP008 Alopecia 53 3.173
113
HPT046 Hepatic Veno-Occlusive Disease 55 3.173
114
P HYP098 Hypereosinophilic Syndrome 66 3.156
115
ANG046 Angioimmunoblastic T-Cell Lymphoma 51 3.103
116
HMG005 Hemoglobinopathy 55 3.090
117
P ANP001 Anaplastic Large Cell Lymphoma 61 3.083
118
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 3.008
119
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 43 3.008
120
P PRR002 Pure Red-Cell Aplasia 46 3.007
121
P CYS018 Cystitis 59 3.005
122
PST046 Post-Transplant Lymphoproliferative Disease 53 2.999
123
DWN001 Down Syndrome 70 2.990
124
c PRM012 Primary Polycythemia 58 2.977
125
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 2.965
126
SCK003 Sickle Cell Anemia 74 2.919
127
P CMP005 Campomelic Dysplasia 65 2.885
128
HMR023 Hemorrhagic Cystitis 43 2.861
129
SPL018 Splenomegaly 47 2.814
130
ATY042 Atypical Chronic Myeloid Leukemia 50 2.789
131
CYT002 Cytokine Deficiency 43 2.786
132
CHL149 Childhood Acute Myeloid Leukemia 42 2.777
133
RFR009 Refractory Cytopenia with Multilineage Dysplasia 30 2.760
134
LRG008 Large Granular Lymphocyte Leukemia 34 2.753
135
P KDN017 Kidney Cancer 60 2.693
136
P LPS004 Lupus Erythematosus 61 2.670
137
P DYS007 Dyskeratosis Congenita 66 2.664
138
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 2.656
139
SPR126 Superior Semicircular Canal Dehiscence 41 2.654
140
c HMG029 Hemoglobin Se Disease 41 2.654
141
LYM048 Lymphoma, Large-Cell, Immunoblastic 27 2.649
142
47X002 47,xyy 48 2.633
143
TCL005 T-Cell Prolymphocytic Leukemia 48 2.614
144
P ESS003 Essential Thrombocythemia 68 2.597
145
RFR002 Refractory Hairy Cell Leukemia 34 2.558
146
P DRR001 Diarrhea 55 2.550
147
LYM051 Lymphomatoid Granulomatosis 44 2.547
148
P AGM001 Agammaglobulinemia 67 2.533
149
PLS016 Plasma Cell Leukemia 53 2.531
150
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.506
151
PST011 Pustulosis of Palm and Sole 52 2.499
152
P PSR002 Psoriasis 63 2.499
153
c THR090 Thrombocythemia 1 50 2.492
154
SRC014 Sarcoma 64 2.437
155
SPN035 Spindle Cell Sarcoma 51 2.437
156
P ENC018 Encephalopathy 62 2.361
157
CHR286 Chronic Neutrophilic Leukemia 42 2.349
158
PRG009 Progressive Multifocal Leukoencephalopathy 58 2.342
159
P GLM007 Glomerulonephritis 59 2.334
160
c BTT014 Beta-Thalassemia 72 2.310
161
c ALP101 Alpha-Thalassemia 62 2.303
162
ADR007 Adrenoleukodystrophy 74 2.299
163
GLB002 Glioblastoma 67 2.249
164
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.240
165
INT054 Intraocular Lymphoma 48 2.230
166
HRP004 Herpes Zoster 60 2.219
167
c SYS001 Systemic Lupus Erythematosus 86 2.196
168
CLD007 Cold Agglutinin Disease 42 2.193
169
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 2.193
170
P KDN018 Kidney Disease 72 2.176
171
P WSK001 Wiskott-Aldrich Syndrome 72 2.162
172
P BCL005 B Cell Prolymphocytic Leukemia 39 2.161
173
GLL048 Glial Tumor 52 2.161
174
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.146
175
P OST001 Osteopetrosis 70 2.142
176
SKN013 Skin Benign Neoplasm 49 2.127
177
CRH001 Crohn's Disease 80 2.113
178
IND016 Indolent B-Cell Non-Hodgkin Lymphoma 19 2.109
179
CHR178 Chromosomal Triplication 34 2.100
180
AGG012 Aggressive Nk-Cell Leukemia 47 2.080
181
P BNG032 Benign Mesothelioma 53 2.074
182
SFT003 Soft Tissue Sarcoma 57 2.068
183
c CHR418 Chronic Leukemia 48 2.032
184
RNL065 Renal Cell Carcinoma, Papillary, 1 79 2.032
185
CHR563 Chronic Eosinophilic Leukemia 48 2.032
186
P PRP019 Peripheral Nervous System Disease 57 2.028
187
THR004 Thrombocytosis 52 2.018
188
c ALM001 Al Amyloidosis 54 2.018
189
CRV035 Cervical Cancer 72 2.013
190
ATX019 Ataxia with Vitamin E Deficiency 44 2.006
191
SCT005 Scott Syndrome 51 1.992
192
GLM045 Glioma 62 1.957
193
P BRS047 Breast Cancer 97 1.953
194
P MST002 Mast-Cell Leukemia 50 1.948
195
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 1.947
196
P GLM040 Glioma Susceptibility 1 70 1.945
197
HRL003 Hurler Syndrome 66 1.941
198
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.937
199
CMB081 Combined Immunodeficiency, X-Linked 39 1.928
200
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 1.928
201
c DMN023 Diamond-Blackfan Anemia 1 68 1.928
202
STM007 Stomatitis 52 1.905
203
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.901
204
P HPT023 Hepatocellular Carcinoma 95 1.898
205
c ADL052 Adult Acute Lymphocytic Leukemia 45 1.890
206
BLR008 Bilirubin Metabolic Disorder 57 1.886
207
SKN016 Skin Disease 62 1.876
208
c ACT071 Acute Kidney Failure 60 1.876
209
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.871
210
P OVR042 Ovarian Cancer 88 1.863
211
PSR001 Psoriatic Arthritis 61 1.859
212
ADR022 Adrenomyeloneuropathy 39 1.847
213
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.843
214
ATM095 Autoimmune Disease 61 1.804
215
CHR682 Chronic Bilirubin Encephalopathy 37 1.802
216
OST159 Osteogenic Sarcoma 66 1.800
217
MRK001 Merkel Cell Carcinoma 65 1.796
218
c INH020 Inherited Metabolic Disorder 47 1.789
219
c HPT016 Hepatitis B 62 1.782
220
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.779
222
P NRB001 Neuroblastoma 66 1.762
223
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.759
225
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.744
226
CHD001 Chediak-Higashi Syndrome 67 1.702
227
BTT017 Beta-Thalassemia Major 53 1.700
228
CHC001 Chickenpox 56 1.697
229
P ATX030 Ataxia-Telangiectasia 80 1.684
230
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.681
231
TLN003 Telangiectasis 51 1.674
232
P ART022 Arthritis 70 1.661
233
P AMY004 Amyloidosis 69 1.661
234
P SKN015 Skin Carcinoma 71 1.659
235
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.652
236
TCL003 T Cell Deficiency 44 1.650
237
MLG079 Malignant Pleural Mesothelioma 42 1.650
238
TXC005 Toxic Shock Syndrome 62 1.645
239
LST001 Listeriosis 59 1.645
240
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.642
241
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.642
242
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.642
243
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.642
244
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.642
245
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.642
246
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.642
247
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.642
248
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.642
249
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.642
250
MYL003 Myeloid Sarcoma 48 1.639
251
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 1.633
252
CD4003 Cd40 Ligand Deficiency 54 1.633
253
RFR004 Refractory Hematologic Cancer 31 1.613
254
STT001 Status Epilepticus 58 1.609
255
c OVR114 Ovarian Cancer 1 60 1.593
256
P PLY019 Polyneuropathy 53 1.592
257
P ADN016 Adenocarcinoma 63 1.592
258
P EPD016 Epidermolysis Bullosa 53 1.592
259
P MLT020 Multiple Sclerosis 79 1.589
260
P PMP001 Pemphigus 55 1.583
261
SCH036 Scheie Syndrome 73 1.581
262
IND017 Indolent Plasma Cell Myeloma 40 1.579
263
NTR005 Nutritional Deficiency Disease 60 1.578
264
DYS164 Dyskeratosis Congenita, X-Linked 56 1.573
265
P LVR013 Liver Disease 68 1.567
266
c MST023 Mesothelioma, Malignant 56 1.554
267
c ACT027 Acute Pancreatitis 60 1.553
268
ALL029 Allergic Disease 61 1.553
269
BCT022 Bacterial Infectious Disease 56 1.548
270
P ASP006 Aspergillosis 71 1.548
271
P NRP001 Neuropathy 59 1.539
272
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.537
273
c CWD006 Cowden Syndrome 1 79 1.527
274
ACT119 Acute Promyelocytic Leukemia 62 1.526
275
c SVR003 Severe Congenital Neutropenia 59 1.521
276
P VSC011 Vasculitis 61 1.511
277
P NPH012 Nephrotic Syndrome 62 1.506
278
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.476
279
P NJM001 Nijmegen Breakage Syndrome 75 1.468
280
ACT250 Acute Megakaryocytic Leukemia 63 1.452
281
AMD002 Amed Syndrome, Digenic 37 1.451
282
KPR003 Keipert Syndrome 44 1.451
283
P PNC044 Pancreatitis 61 1.448
284
SQM006 Squamous Cell Carcinoma 59 1.448
285
PRN049 Paraneoplastic Pemphigus 44 1.448
286
P PNC035 Pancreatic Cancer 86 1.439
287
AMG001 Amegakaryocytic Thrombocytopenia, Congenital 55 1.435
288
P HPT021 Hepatitis 68 1.435
289
NDL024 Nodal Marginal Zone Lymphoma 37 1.429
290
P PNM007 Pneumonia 64 1.429
291
PLS011 Plasmacytoma 56 1.422
292
c SCL052 Scleroderma, Familial Progressive 60 1.416
293
P RSP003 Respiratory Failure 74 1.403
294
ERY051 Erythroleukemia, Familial 37 1.397
295
P MLG074 Malignant Mesenchymoma 40 1.394
296
c HPT003 Hepatitis a 63 1.392
297
PRT251 Proteinuria, Chronic Benign 58 1.390
298
HYP014 Hyperuricemia 51 1.376
299
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 52 1.373
300
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.373
301
P PRS038 Personality Disorder 65 1.373
302
VSL002 Visual Epilepsy 39 1.373
303
P CRV039 Cervicitis 52 1.373
304
CMM004 Common Variable Immunodeficiency 72 1.373
305
P SZR006 Seizure Disorder 69 1.373
306
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.362
307
P BLD134 Bladder Cancer 79 1.358
308
c WLM013 Wilms Tumor 1 65 1.358
309
BRN004 Brain Edema 54 1.358
310
P EPD009 Epidermolysis Bullosa Dystrophica 66 1.358
311
HST010 Histiocytosis 49 1.354
312
P SYS005 Systemic Scleroderma 73 1.354
313
c MCL013 Mucolipidosis Iv 64 1.350
314
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 1.350
315
c PSR032 Psoriasis 11 47 1.350
316
CHP002 Chops Syndrome 47 1.350
317
c DRR009 Diarrhea 6 46 1.350
318
c PSR023 Psoriasis 1 52 1.350
319
c PSR018 Psoriasis 13 40 1.350
320
c PSR028 Psoriasis 7 43 1.350
321
NSL029 Nasal Type Extranodal Nk/t-Cell Lymphoma 41 1.350
322
c PSR017 Psoriasis 2 53 1.350
323
LNG031 Lung Benign Neoplasm 51 1.345
324
IND005 Indolent B Cell Lymphoma 20 1.344
325
FCT007 Factor Vii Deficiency 64 1.333
326
P RFR014 Refractory Anemia with Excess Blasts Type 2 18 1.330
327
RFR015 Refractory Anemia with Excess Blasts Type 1 15 1.330
328
LNG108 Langerhans Cell Histiocytosis 57 1.329
329
END086 End Stage Renal Disease 54 1.329
330
CRY004 Cryoglobulinemia 47 1.299
331
ISC004 Ischemia 61 1.297
332
INT395 Intracranial Meningioma 48 1.296
333
P CNT005 Central Nervous System Lymphoma 51 1.296
334
MNN043 Meningioma, Familial 79 1.296
335
SCR001 Secretory Meningioma 40 1.296
336
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.296
337
OCL022 Ocular Melanoma 54 1.290
338
TCL024 T-Cell Non-Hodgkin Lymphoma 39 1.290
339
c OST131 Osteopetrosis, Autosomal Dominant 2 52 1.287
340
c SYS043 Systemic Lupus Erythematosus 1 38 1.287
341
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 51 1.287
342
VGN017 Vaginal Cancer 58 1.287
343
EXT010 Extramedullary Plasmacytoma 46 1.287
344
PRP030 Purpura 54 1.272
345
TTT001 Tatton-Brown-Rahman Syndrome 45 1.253
346
LYM052 Lymphomatoid Papulosis 37 1.253
347
PNM001 Pneumocystosis 60 1.230
348
c SML038 Small Cell Cancer of the Lung 69 1.224
349
DFF003 Diffuse Scleroderma 41 1.224
350
c MCP050 Mucopolysaccharidosis, Type Ii 73 1.217
351
MTB004 Metabolic Acidosis 48 1.215
352
P DMY001 Demyelinating Polyneuropathy 41 1.215
353
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.210
354
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.185
355
P TRC086 Trichohepatoenteric Syndrome 1 60 1.185
356
P RHM011 Rheumatoid Arthritis 81 1.185
357
CHD004 Chudley-Mccullough Syndrome 47 1.185
358
CRB009 Cerebritis 43 1.185
359
P MMB011 Membranous Nephropathy 50 1.184
360
P HVY001 Heavy Chain Disease 32 1.167
361
P MLN069 Melanoma, Uveal 59 1.158
362
P CTR002 Cataract 59 1.158
363
P LNG032 Lung Cancer 98 1.153
364
PNN001 Panniculitis 52 1.149
365
OVR094 Ovarian Epithelial Cancer 39 1.148
366
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 1.147
367
P CND004 Candidiasis 57 1.140
368
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 29 1.133
369
END057 Endometrial Cancer 71 1.125
370
P RHB003 Rhabdomyosarcoma 66 1.124
371
P GST053 Gastric Cancer 82 1.120
372
LTT002 Letterer-Siwe Disease 33 1.120
373
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 1.120
374
IMM136 Immune System Disease 46 1.120
375
c CNT035 Central Nervous System Disease 53 1.118
376
P CRY007 Cryoglobulinemia, Familial Mixed 49 1.109
377
GST045 Gastroenteritis 58 1.109
378
VRL011 Viral Infectious Disease 60 1.106
379
P MNN013 Meningitis 65 1.089
380
INV001 Invasive Aspergillosis 48 1.088
381
c ACT134 Acute Liver Failure 57 1.087
382
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 1.066
383
P ESP024 Esophagitis 60 1.063
384
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 1.059
385
c PNS012 Paine Syndrome 60 1.053
386
P SPP010 Suppressor of Tumorigenicity 3 51 1.053
387
AYM001 Ayme-Gripp Syndrome 57 1.053
388
c SPN225 Spondyloarthropathy 1 70 1.053
389
c SPN330 Spondylocostal Dysostosis 5 55 1.053
390
c MYL058 Myeloproliferative Syndrome, Transient 46 1.053
391
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.053
392
c PST022 Posterior Uveal Melanoma 41 1.053
393
SYN007 Synovitis 54 1.053
394
PPL022 Papilloma 53 1.053
395
SQM002 Squamous Cell Papilloma 45 1.053
396
PLC002 Plica Syndrome 35 1.053
397
P PRT026 Parotitis 42 1.053
398
FBR002 Fibrosarcoma of Bone 47 1.053
399
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.053
400
CHL079 Children's Interstitial Lung Disease 26 1.053
401
P ALP009 Alopecia Areata 59 1.053
402
PGM030 Pigmentation Anomaly of the Skin 24 1.053
403
GST071 Gastrointestinal Carcinoma 46 1.051
404
FLL027 Fallopian Tube Carcinoma 66 1.051
405
HGH043 High Grade Glioma 46 1.051
406
MXD026 Mixed Glioma 45 1.051
407
THR123 Thrombotic Microangiopathy 40 1.044
409
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 1.038
410
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 1.038
411
P HRP006 Herpes Simplex 65 1.027
412
ACQ007 Acquired Immunodeficiency Syndrome 58 1.010
413
BLS007 Blastic Plasmacytoid Dendritic Cell 37 0.998
414
DND018 Dendritic Cell Tumor 41 0.998
415
BRN024 Bronchitis 67 0.992
416
SNS003 Sensory Peripheral Neuropathy 51 0.992
417
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.976
418
EWN003 Ewing Sarcoma 70 0.976
419
ACT011 Acute Contagious Conjunctivitis 42 0.976
420
P HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.976
421
P CNJ013 Conjunctivitis 66 0.976
422
BRN028 Brain Cancer 73 0.976
423
GST049 Gastrointestinal System Cancer 49 0.976
424
APH002 Aphasia 55 0.973
425
CNS004 Constipation 56 0.973
426
LNG013 Lung Lymphoma 31 0.973
427
P PRM293 Primary Mediastinal B-Cell Lymphoma 42 0.970
428
CRY014 Cryptococcal Meningitis 48 0.957
429
P URN019 Urinary Tract Infection 49 0.953
430
CRT012 Cortical Blindness 42 0.953
431
P AVS003 Avascular Necrosis 41 0.953
432
P PRS040 Prostate Cancer 95 0.951
433
c PRS130 Prostate Cancer, Hereditary, 8 32 0.951
434
c PRS136 Prostate Cancer, Hereditary, 6 33 0.951
435
PRS047 Prostatitis 58 0.951
436
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 22 0.943
437
P ADL010 Adult Respiratory Distress Syndrome 71 0.930
438
P TXP001 Toxoplasmosis 60 0.930
439
c ACQ016 Acquired Pure Red Cell Aplasia 29 0.930
440
LNG099 Lung Disease 62 0.924
441
OST017 Osteomyelitis 63 0.906
442
LKP003 Leukoplakia 39 0.906
443
P INF038 Influenza 68 0.906
444
c PRM304 Primary Hemophagocytic Lymphohistiocytosis 25 0.906
445
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.898
446
HRL004 Hurler-Scheie Syndrome 58 0.898
447
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.893
448
P NSP012 Nasopharyngeal Carcinoma 60 0.893
449
P INH011 Inherited Bone Marrow Failure Syndromes 34 0.890
450
c MLT068 Multiple Mitochondrial Dysfunctions Syndrome 1 45 0.890
451
P MLT027 Multiple Mitochondrial Dysfunctions Syndrome 37 0.890
452
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 0.890
453
P CLR023 Colorectal Cancer 100 0.890
454
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 50 0.890
455
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 0.890
456
P LYM024 Lymphatic System Disease 46 0.890
457
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.890
458
P PRD037 Periodontal Ehlers-Danlos Syndrome 44 0.890
459
ACT118 Acute Non Lymphoblastic Leukemia 26 0.890
460
P MTC003 Metachromatic Leukodystrophy 71 0.881
461
P LKD001 Leukodystrophy 58 0.881
462
P KRB001 Krabbe Disease 69 0.881
463
CHR208 Chromosome 17p Deletion 21 0.881
464
P SML001 Small Cell Carcinoma 52 0.878
465
CNG034 Congestive Heart Failure 69 0.878
466
BNM005 Bone Marrow Necrosis 25 0.878
467
GLM044 Glomerular Disease 34 0.878
468
P RTN024 Retinoblastoma 72 0.870
469
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.870
470
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.865
471
PLR008 Pleurisy 49 0.844
472
HMN047 Human Cytomegalovirus Infection 59 0.840
473
CHL065 Cholangiocarcinoma 58 0.837
474
INT079 Intrahepatic Cholangiocarcinoma 51 0.837
475
HMS001 Hemosiderosis 48 0.823
476
HYP266 Hypoxia 56 0.823
477
c BCT013 Bacterial Pneumonia 47 0.823
478
P RRH023 Rare Hereditary Hemochromatosis 53 0.823
479
SRC027 Sarcoma, Synovial 58 0.821
480
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.806
481
P DRM010 Dermatomyositis 61 0.806
482
MSL001 Measles 61 0.806
483
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.806
484
IMM078 Immunodeficiency 21 57 0.804
485
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.804
486
AGM019 Agammaglobulinemia, X-Linked 72 0.804
487
P PLM036 Pulmonary Fibrosis 65 0.804
488
NNS057 Non-Severe Combined Immunodeficiency 13 0.801
489
ATM052 Autoimmune Disease 1 36 0.789
490
P MDL005 Medulloblastoma 75 0.789
491
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 31 0.789
492
RDD003 Riddle Syndrome 58 0.789
493
MST024 Mastocytosis, Cutaneous 66 0.789
494
P MLN066 Melanoma, Cutaneous Malignant 1 66 0.789
495
RBR002 Roberts-Sc Phocomelia Syndrome 63 0.789
496
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 0.789
497
VLV032 Vulva Cancer 60 0.789
498
ADN009 Adenosquamous Carcinoma 49 0.789
499
NRN004 Neuroendocrine Tumor 55 0.789
500
SML008 Small Intestine Lymphoma 33 0.789
501
PNL012 Penile Cancer 57 0.789
502
RHB001 Rhabdoid Cancer 68 0.789
503
MDS022 Mediastinitis 47 0.789
504
CRC021 Carcinosarcoma 62 0.789
505
INT253 Intestinal Benign Neoplasm 46 0.789
506
P EPN001 Ependymoblastoma 44 0.789
507
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.789
508
P PLY041 Polymyositis 59 0.788
509
P MYS005 Myositis 56 0.788
510
DMY004 Demyelinating Disease 50 0.788
511
PRT036 Peritonitis 65 0.783
512
NRR001 Neuroretinitis 42 0.769
513
ERY003 Erythema Multiforme 56 0.769
514
SVR097 Severe Cutaneous Adverse Reaction 68 0.769
515
BRN012 Bronchiolitis Obliterans 56 0.769
516
BRN002 Bronchiolitis 57 0.769
517
RTN023 Retinitis 45 0.769
518
P SHW006 Shwachman-Diamond Syndrome 1 66 0.769
519
ERY066 Erythema Multiforme Major 29 0.769
520
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.769
521
c MCL062 Mucolipidosis Ii Alpha/beta 69 0.761
522
GLN010 Glanzmann Thrombasthenia 66 0.761
523
THR035 Thrombasthenia 48 0.761
524
P NRV007 Nervous System Disease 66 0.761
525
OCL069 Ocular Motor Apraxia 57 0.749
526
c THR102 Thrombocytopenia 5 29 0.749
527
CRB004 Cerebral Artery Occlusion 46 0.749
528
HYP025 Hyperphosphatemia 47 0.749
529
CRY005 Cryptococcosis 61 0.749
530
c OST126 Osteopetrosis, Autosomal Recessive 1 51 0.749
531
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 0.749
532
CHL061 Childhood Leukemia 47 0.749
533
ETV001 Etv6 Thrombocytopenia and Predisposition to Leukemia 31 0.749
534
c ATS282 Autosomal Recessive Malignant Osteopetrosis 45 0.749
535
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.733
536
FCS002 Fucosidosis 62 0.733
537
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 36 0.733
538
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.733
539
RFS006 Refsum Disease, Classic 63 0.733
540
c MCP049 Mucopolysaccharidosis, Type Vii 62 0.733
541
P FTL069 Fetal Akinesia Deformation Sequence 1 63 0.733
542
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.733
543
ASP002 Aspartylglucosaminuria 57 0.733
544
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 54 0.733
545
BRN139 Brain Small Vessel Disease 1 with or Without Ocular Anomalies 54 0.733
546
SPH010 Sphingolipidosis 47 0.733
547
KRT002 Keratomalacia 54 0.733
548
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.733
549
MCP033 Mucopolysaccharidoses 44 0.733
550
ZLL011 Zellweger Spectrum Disorder 45 0.733
551
P ZLL001 Zellweger Syndrome 65 0.733
552
PRX001 Peroxisomal Disease 46 0.733
553
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.733
554
P MYS003 Myasthenia Gravis 68 0.726
555
CYT005 Cytomegalovirus Retinitis 50 0.726
556
DSS009 Disseminated Intravascular Coagulation 56 0.726
557
NWC001 Newcastle Disease 48 0.726
558
GST040 Gastric Adenocarcinoma 66 0.726
559
RYN005 Raynaud Phenomenon 45 0.726
560
EVN001 Evans' Syndrome 46 0.726
561
c LKM070 Leukemia, Acute Monocytic 56 0.715
562
CLR030 Clear Cell Renal Cell Carcinoma 54 0.715
563
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.702
564
c VRL010 Viral Hepatitis 52 0.702
565
NRT004 Neuritis 53 0.702
566
BRN014 Bronchopneumonia 52 0.702
567
P UVT001 Uveitis 57 0.702
568
P OPT009 Optic Neuritis 57 0.702
569
LST003 Listeria Meningitis 29 0.702
570
PNC129 Pancreatic Adenocarcinoma 65 0.702
571
PRS063 Paresthesia 39 0.702
572
HYP005 Hypokalemia 55 0.702
573
c ACQ014 Acquired Hemophilia 45 0.702
574
c PRM301 Primary Cutaneous T-Cell Lymphoma 35 0.702
575
PRM133 Primary Pulmonary Lymphoma 16 0.702
576
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.702
577
DSS032 Disease by Infectious Agent 55 0.674
578
GST027 Gastric Lymphoma 44 0.674
579
c VRL005 Viral Pneumonia 52 0.674
580
OTT002 Otitis Media 71 0.674
581
BCT021 Bacterial Sepsis 43 0.674
582
CYN002 Cyanosis, Transient Neonatal 43 0.674
583
CLT003 Colitis 63 0.674
584
EXT033 Extrapulmonary Tuberculosis 45 0.674
585
P ESN008 Eosinophilic Pneumonia 50 0.674
586
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.674
587
P GLL022 Guillain-Barre Syndrome 59 0.674
588
P FCL005 Focal Segmental Glomerulosclerosis 57 0.674
589
DPH001 Diphtheria 59 0.674
590
P MYC008 Myocarditis 59 0.674
591
P TRM003 Tremor 50 0.674
592
c JVN010 Juvenile Rheumatoid Arthritis 66 0.674
594
ORL012 Oral Leukoplakia 35 0.674
595
P CHN012 Chondrosarcoma 56 0.656
596
VLC001 Velocardiofacial Syndrome 57 0.656
597
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 0.656
598
CRN241 Corneal Dystrophy, Congenital Stromal 49 0.656
599
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 35 0.656
600
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.656
601
BNS007 Bone Sarcoma 51 0.656
602
ALC007 Alcohol Dependence 65 0.656
603
BHC003 Behcet Syndrome 71 0.656
604
c HYP829 Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive 42 0.656
605
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 47 0.656
606
MTP028 Metaphyseal Dysplasia, Spahr Type 34 0.656
607
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.656
608
IMM222 Immunodeficiency 67 42 0.656
609
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 31 0.656
610
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 54 0.656
611
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.656
612
MYX005 Myxoid Liposarcoma 65 0.656
613
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.656
614
MNN042 Meningioma, Radiation-Induced 51 0.656
615
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.656
616
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 0.656
617
P SJG008 Sjogren Syndrome 61 0.656
618
GLS018 Glass Syndrome 60 0.656
619
c BNM010 Bone Marrow Failure Syndrome 1 37 0.656
620
DGR001 Digeorge Syndrome 62 0.656
621
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.656
622
P BNC003 Bone Cancer 58 0.656
623
P ALC033 Alcohol Use Disorder 67 0.656
624
c HMG001 Hemoglobin C Disease 41 0.656
625
IDP011 Idiopathic Interstitial Pneumonia 59 0.656
626
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.656
627
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.656
628
HGH044 High Grade Ependymoma 40 0.656
629
ANP006 Anaplastic Ependymoma 46 0.656
630
GLM004 Gliomatosis Cerebri 52 0.656
631
P BNG030 Benign Ependymoma 51 0.656
632
P BNG095 Benign Giant Cell Tumor 43 0.656
633
END035 Endocrine Gland Cancer 42 0.656
634
c MLG084 Malignant Fibrous Histiocytoma 62 0.656
635
HMN048 Human Papillomavirus Infectious Disease 46 0.656
636
P PRP021 Peripheral Nervous System Neoplasm 37 0.656
637
SPN021 Spinal Meningioma 43 0.656
638
ACT029 Acute Interstitial Pneumonia 59 0.656
639
GLS001 Gliosarcoma 63 0.656
640
SPN043 Spinal Cord Glioma 31 0.656
641
LNG039 Lung Squamous Cell Carcinoma 57 0.656
642
P MST009 Mastocytosis 64 0.656
643
NRF003 Neurofibrosarcoma 43 0.656
644
SMT002 Smooth Muscle Tumor 38 0.656
645
c ATM017 Autoimmune Disease of the Nervous System 37 0.656
646
P BRN035 Brain Stem Glioma 49 0.656
647
APP009 Appendix Adenocarcinoma 47 0.656
648
VLV036 Vulvar Disease 47 0.656
649
VGN023 Vaginitis 56 0.656
650
P LPS002 Liposarcoma 64 0.656
651
CYS014 Cystadenocarcinoma 51 0.656
652
SRS001 Serous Cystadenocarcinoma 51 0.656
653
P GLL018 Gallbladder Cancer 53 0.656
654
DNM004 Dnmt3a Overgrowth Syndrome 17 0.656
655
BNG036 Bone Giant Cell Tumor 48 0.656
656
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.656
657
P INS002 in Situ Carcinoma 53 0.656
658
DCK002 Dock8 Immunodeficiency Syndrome 25 0.656
659
CRV002 Cervix Uteri Carcinoma in Situ 48 0.656
660
CLL010 Cellular Ependymoma 58 0.656
661
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.656
662
CLR003 Clear Cell Adenocarcinoma 50 0.656
663
P PLM034 Pulmonary Emphysema 58 0.656
664
CRV045 Cervical Intraepithelial Neoplasia 38 0.656
665
CHR176 Chromophil Renal Cell Carcinoma 23 0.656
666
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.656
667
DSM007 Desmoplastic Small Round Cell Tumor 54 0.656
668
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.656
669
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.656
670
NRM001 Neuromyelitis Optica 60 0.656
671
PLS037 Plasma Cell Tumor 20 0.656
672
HYP017 Hypophosphatemia 49 0.640
673
c GMM003 Gamma Heavy Chain Disease 37 0.640
674
c THR125 Thrombocytopenia 7 22 0.640
675
CRD132 Cardiac Conduction Defect 59 0.640
676
HMP005 Hemiplegia 53 0.640
677
MMB001 Membranoproliferative Glomerulonephritis 56 0.640
678
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 19 0.640
679
ANS011 Anus Cancer 55 0.640
680
ANS025 Anus Benign Neoplasm 28 0.640
681
P HYP086 Hypothyroidism 69 0.634
682
HYP088 Hyper-Igd Syndrome 51 0.597
683
P OCL002 Oculocutaneous Albinism 59 0.597
684
INT072 Intestinal Pseudo-Obstruction 60 0.597
685
c DWL002 Dowling-Degos Disease 1 58 0.597
686
c ATS384 Autosomal Dominant Non-Syndromic Intellectual Disability 2 28 0.597
687
MLG169 Malignant Astrocytoma 57 0.597
688
PLM001 Pulmonary Tuberculosis 69 0.597
689
c ATM011 Autoimmune Hepatitis 62 0.597
690
CNT007 Central Nervous System Tuberculosis 35 0.597
691
P ART023 Arthropathy 60 0.597
692
SPS057 Spasticity 43 0.597
693
IRD001 Iridocyclitis 54 0.597
694
CMP001 Composite Lymphoma 36 0.597
695
ERY002 Erythema Infectiosum 36 0.597
696
ALB002 Albinism 47 0.597
697
MLR002 Miliary Tuberculosis 47 0.597
698
c BCT007 Bacterial Meningitis 55 0.597
699
PMP008 Pemphigus Vegetans 27 0.597
700
CRB138 Core Binding Factor Acute Myeloid Leukemia 44 0.597
701
THY029 Thyroid Carcinoma 54 0.557
702
P THY032 Thyroiditis 56 0.554
703
c INF071 Inflammatory Bowel Disease 1 65 0.554
704
CRH005 Crohn's Colitis 53 0.554
705
ACT098 Acute Erythroid Leukemia 55 0.554
706
MCR225 Macrophage Activation Syndrome 45 0.546
707
P HMP007 Hemophilia 52 0.518
708
WST005 West Nile Virus 55 0.492
709
P PLM037 Pulmonary Hypertension 69 0.492
710
BRC012 Brucellosis 66 0.492
711
CRS001 Crescentic Glomerulonephritis 42 0.492
712
LYM021 Lymphadenitis 56 0.492
713
EPD005 Epidural Abscess 31 0.492
714
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.492
715
NCR004 Nocardiosis 52 0.492
716
P END047 Endophthalmitis 53 0.492
717
WST010 West Nile Virus Infection 32 0.492
718
INT221 Intravascular Large B-Cell Lymphoma 37 0.492
719
LKC009 Leukocyte Adhesion Deficiency, Type I 70 0.484
720
c CHR684 Chronic Kidney Disease 74 0.484
721
THY030 Thyroid Gland Disease 50 0.452
722
TRN018 Transitional Cell Carcinoma 56 0.452
723
THY122 Thyroid Gland Cancer 59 0.452
724
BLD131 Bladder Urothelial Carcinoma 59 0.452
725
c HMP029 Hemophilia a 69 0.441
726
P TST021 Testicular Germ Cell Tumor 61 0.441
727
NSP002 Nasopharyngitis 45 0.441
728
c TYP008 Type 1 Diabetes Mellitus 77 0.441
729
FCT001 Factor Viii Deficiency 62 0.441
730
P LNG064 Lung Cancer Susceptibility 3 70 0.441
731
LYS002 Lysosomal Storage Disease 51 0.441
732
P DBT009 Diabetes Mellitus 67 0.441
733
c TYP009 Type 2 Diabetes Mellitus 92 0.336
734
ESP021 Esophageal Cancer 84 0.336
735
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.336
736
TKY002 Takayasu Arteritis 61 0.336
737
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 0.336
738
MRG013 Mirage Syndrome 45 0.336
739
c GCH016 Gaucher Disease, Type Ii 53 0.336
740
CNN010 Connective Tissue Benign Neoplasm 44 0.336
741
HMN044 Human Immunodeficiency Virus Type 1 76 0.336
742
c LYS019 Loeys-Dietz Syndrome 1 58 0.336
743
TST018 Testicular Yolk Sac Tumor 39 0.336
744
P END039 Endodermal Sinus Tumor 42 0.336
745
BRN005 Brain Glioblastoma Multiforme 34 0.336
746
SYS004 Systemic Mastocytosis 62 0.336
747
SPN041 Spinal Cord Disease 54 0.336
748
BLR013 Biliary Tract Cancer 43 0.336
749
ORP003 Oropharynx Cancer 54 0.336
750
ATY022 Atypical Coarctation of Aorta 34 0.336
751
CLS052 Classic Hairy Cell Leukemia 25 0.336
752
ENG004 Engraftment Syndrome 26 0.331
753
GRM005 Germ Cell Cancer 46 0.320
754
IRN002 Iron Metabolism Disease 56 0.320
755
PRT035 Peritoneum Cancer 45 0.320
756
FBR086 Fibrolamellar Carcinoma 59 0.320
757
HPT022 Hepatoblastoma 54 0.320
758
IRR002 Irritable Bowel Syndrome 65 0.320
759
ATS010 Autosomal Recessive Disease 42 0.256
760
HYP063 Hypersplenism 52 0.256
761
DRG002 Drug-Induced Hepatitis 42 0.256
762
DRM006 Dermatitis 62 0.256
763
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.234
764
CHR074 Choriocarcinoma 46 0.234
765
HYP066 Hyperglycemia 60 0.234
766
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 66 0.234
767
ADN001 Adenosine Deaminase Deficiency 59 0.234
768
CHR276 Chronic Active Epstein-Barr Virus Infection 41 0.234
769
DFF031 Diffuse Alveolar Hemorrhage 31 0.234
770
P TMR010 Tumor Predisposition Syndrome 69 0.209
771
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.209
772
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.209
773
URM002 Uremia 47 0.209
774
MCR141 Mucormycosis 59 0.209
775
INH023 Inherited Cancer-Predisposing Syndrome 53 0.209
776
NDL020 Nodal Marginal Zone B-Cell Lymphoma 29 0.209
777
c MCR133 Microvascular Complications of Diabetes 4 41 0.181
778
LG4001 Lig4 Syndrome 55 0.181
779
BNR002 Bone Resorption Disease 47 0.181
781
P GRS003 Griscelli Syndrome 53 0.181
782
c MCR113 Microvascular Complications of Diabetes 3 52 0.181
783
c MCR130 Microvascular Complications of Diabetes 6 41 0.181
784
c MCR120 Microvascular Complications of Diabetes 7 47 0.181
785
LYM114 Lymphoproliferative Syndrome, X-Linked, 2 51 0.181
786
HSH003 Hashimoto Thyroiditis 60 0.181
787
c BSL007 Basal Cell Carcinoma 68 0.181
788
HMP001 Hemopericardium 47 0.181
789
P PRC012 Pericardial Effusion 50 0.181
790
CLL003 Cellulitis 53 0.181
791
MYC021 Mycobacterium Xenopi 19 0.181
792
P ENC004 Encephalitis 61 0.181
793
P PLY188 Polyendocrinopathy 29 0.181
794
DRG014 Drug-Induced Autoimmune Hemolytic Anemia 20 0.181
795
ATM069 Autoimmune Hemolytic Anemia, Warm Type 26 0.181
796
P ALZ034 Alzheimer Disease 87 0.148
797
CHR072 Chordoma 57 0.148
798
c HMC039 Hemochromatosis, Type 1 73 0.148
799
c HMP013 Hemophagocytic Lymphohistiocytosis, Familial, 3 47 0.148
800
RTC012 Reticuloendotheliosis, X-Linked 35 0.148
801
GLC106 Glucocorticoid Resistance, Generalized 48 0.148
802
OST003 Osteonecrosis 61 0.148
803
NKC002 Nk Cell Deficiency 31 0.148
804
PRM013 Premature Menopause 57 0.148
805
P CLC063 Celiac Disease 1 66 0.148
806
ENT011 Enterocolitis 55 0.148
807
RNL077 Renal Fibrosis 46 0.148
808
P CRD119 Cardiac Arrest 68 0.148
809
SCR003 Secretory Diarrhea 35 0.148
810
c GRS014 Griscelli Syndrome, Type 2 51 0.148
811
c HPT073 Hepatitis C Virus 71 0.148
812
CHR635 Chromosome 5q Deletion Syndrome 50 0.148
813
C1Q001 C1q Deficiency 39 0.148
814
LYM094 Lymphedema, Primary, with Myelodysplasia 40 0.148
815
P MYM013 Moyamoya Disease 1 60 0.148
816
P LFR001 Li-Fraumeni Syndrome 73 0.148
817
c THR037 Thrombocytopenia 2 37 0.148
818
c THR092 Thrombophilia Due to Thrombin Defect 74 0.148
819
P BND020 Bone Disease 60 0.148
820
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.148
821
MNN009 Meningoencephalitis 48 0.148
822
c ACT068 Acute Cystitis 61 0.148
823
CHL068 Cholestasis 61 0.148
824
SVR001 Severe Acute Respiratory Syndrome 68 0.148
825
P SBS003 Substance Abuse 54 0.148
826
P ANT006 Antiphospholipid Syndrome 55 0.148
827
P VSC007 Vascular Disease 62 0.148
828
P GCH001 Gaucher's Disease 69 0.148
829
ACT017 Acute Chest Syndrome 50 0.148
830
P OBS001 Obstructive Jaundice 49 0.148
831
P LCT001 Lactic Acidosis 50 0.148
832
INT066 Interstitial Lung Disease 60 0.148
833
CLN015 Colon Adenocarcinoma 64 0.148
834
P PLY020 Polyradiculoneuropathy 47 0.148
835
OVR059 Ovary Adenocarcinoma 49 0.148
836
CHR063 Chronic Mucocutaneous Candidiasis 68 0.148
837
GST019 Gastrointestinal Stromal Tumor 78 0.148
838
TCL008 T-Cell Lymphoma 1a 17 0.148
839
P SDR003 Sideroblastic Anemia 49 0.148
840
P ATM020 Autoimmune Enteropathy 34 0.148
841
APP008 Appendicitis 62 0.148
842
ILS001 Ileus 49 0.148
844
MLT075 Multifocal Motor Neuropathy 45 0.148
845
NCR009 Necrobiotic Xanthogranuloma 25 0.148
846
GST014 Gastrointestinal Lymphoma 30 0.148
847
RFR013 Refractory Celiac Disease 33 0.148
848
CMP102 Complications After Hematopoietic Stem Cell Transplantation 21 0.148
849
PRM163 Primary Mediastinal Large B-Cell Lymphoma 40 0.148
850
SVR055 Severe Immune-Mediated Enteropathy 22 0.148
851
ART140 Arteries, Anomalies of 52 0.105
852
P SCH015 Schizophrenia 74 0.105
853
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.105
854
HLC007 Helicobacter Pylori Infection 67 0.105
855
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 54 0.105
856
WRN001 Werner Syndrome 69 0.105
857
SVR066 Severe Combined Immunodeficiency, X-Linked 65 0.105
858
VSC052 Vasculitis, Lymphocytic, Nodular 23 0.105
859
VRC005 Varicose Veins 59 0.105
860
c BRN108 Branchiootic Syndrome 1 63 0.105
861
GRN037 Granulomatosis with Polyangiitis 67 0.105
862
SVR098 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Positive 47 0.105
863
IMM179 Immunodeficiency 31c 54 0.105
864
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.105
865
LPP008 Lipoprotein Quantitative Trait Locus 65 0.105
866
HLX001 Helix Syndrome 47 0.105
867
VRL003 Variola Major 43 0.105
868
P INF037 Inflammatory Bowel Disease 53 0.105
869
c PRM108 Primary Progressive Multiple Sclerosis 51 0.105
870
P SNS001 Sensorineural Hearing Loss 59 0.105
871
P PLY014 Polycystic Kidney Disease 71 0.105
872
P MCL001 Mucolipidosis 49 0.105
873
HYP458 Hyper Ige Syndrome 60 0.105
874
THL010 Thalassemia Minor 31 0.105
875
IMM011 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 52 0.105
876
SLP001 Sleeping Sickness 56 0.105
877
XRP001 Xerophthalmia 42 0.105
878
PLY150 Polykaryocytosis Inducer 29 0.105
879
c ATR087 Atrial Standstill 1 74 0.105
880
FLT011 Felty Syndrome 51 0.105
881
CTR172 Citrullinemia, Classic 64 0.105
882
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.105
883
P FML011 Familial Adenomatous Polyposis 71 0.105
884
BCL011 Bacillary Angiomatosis 29 0.105
885
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.105
886
CRS005 Crest Syndrome 36 0.105
887
PNC005 Penicilliosis 30 0.105
888
CRY001 Cryptogenic Organizing Pneumonia 53 0.105
889
SCN049 Second-Degree Atrioventricular Block 34 0.105
890
P GLL020 Gallbladder Disease 57 0.105
891
DFF010 Diffuse Alopecia Areata 23 0.105
892
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.105
893
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 0.105
894
INC002 Inclusion Body Myositis 57 0.105
895
KPS004 Kaposi Sarcoma 76 0.105
896
PFF001 Pfeiffer Syndrome 77 0.105
897
PRN011 Pernicious Anemia 52 0.105
898
CRT045 Creatine Phosphokinase, Elevated Serum 39 0.105
899
c NRB011 Neuroblastoma 4 13 0.105
900
IMM178 Immunodeficiency 31b 40 0.105
901
c CND037 Candidiasis, Familial, 6 35 0.105
902
MNT320 Mental Retardation, Autosomal Dominant 6, with or Without Seizures 26 0.105
903
c PRG020 Paragangliomas 3 39 0.105
904
c LFR007 Li-Fraumeni Syndrome 2 44 0.105
905
IMM182 Immunodeficiency 31a 28 0.105
906
c LYM107 Lymphoproliferative Syndrome 2 48 0.105
907
HYD002 Hydronephrosis 58 0.105
908
HPT004 Hepatic Coma 43 0.105
909
P HML001 Hemolytic-Uremic Syndrome 52 0.105
910
DYS018 Dysostosis 43 0.105
911
CLC006 Calcinosis 47 0.105
912
c ACQ017 Acquired Von Willebrand Syndrome 48 0.105
913
DRY001 Dry Eye Syndrome 49 0.105
914
c ATS386 Autosomal Dominant Non-Syndromic Intellectual Disability 4 20 0.105
915
c ATS388 Autosomal Dominant Non-Syndromic Intellectual Disability 6 32 0.105
916
P PTS002 Ptosis 52 0.105
917
P SCK004 Seckel Syndrome 58 0.105
918
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.105
919
ATR057 Atrioventricular Block 54 0.105
920
c HRD202 Hereditary Lymphedema I 55 0.105
921
MNN017 Mononeuropathy 41 0.105
922
BLR001 Biliary Atresia 55 0.105
923
KRT001 Keratoconjunctivitis Sicca 49 0.105
924
LKS001 Leukostasis 40 0.105
925
LPD008 Lipid Metabolism Disorder 61 0.105
926
P END044 Endometriosis 62 0.105
927
CRB039 Cerebrovascular Disease 65 0.105
928
P PRL003 Proliferative Glomerulonephritis 43 0.105
929
LVR012 Liver Cirrhosis 62 0.105
930
P INF032 Infertility 60 0.105
931
PRP016 Paraplegia 52 0.105
932
P INT068 Intestinal Disease 53 0.105
933
CNN005 Connective Tissue Disease 66 0.105
934
PLM032 Pulmonary Blastoma 47 0.105
935
EMB002 Embryoma 37 0.105
936
P OVR046 Ovarian Cyst 44 0.105
937
P OVR049 Ovarian Disease 50 0.105
938
ESP002 Esophageal Varix 51 0.105
939
MNN002 Mononeuritis Multiplex 38 0.105
940
c HPT001 Hepatitis C 61 0.105
941
INT071 Intestinal Perforation 49 0.105
942
HST011 Histoplasmosis 54 0.105
943
PLY010 Polyclonal Hypergammaglobulinemia 35 0.105
944
HYP080 Hypogonadism 49 0.105