Search results for rituximab

1392 hits were found for rituximab

# Family MCID Name MIFTS Score
1
P LYM118 Lymphoma 68 0.915
2
P BCL017 B-Cell Lymphoma 58 0.844
3
LYM019 Lymphosarcoma 46 0.777
4
DFF005 Diffuse Large B-Cell Lymphoma 55 0.682
5
LYM133 Lymphoma, Hodgkin, Classic 69 0.674
6
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.632
7
P FLL037 Follicular Lymphoma 67 0.618
8
P LKM071 Leukemia, Chronic Lymphocytic 79 0.576
9
c PRM038 Primary Agammaglobulinemia 44 0.473
10
P LKM002 Leukemia 68 0.457
11
MNT001 Mantle Cell Lymphoma 69 0.453
12
P NTR004 Neutropenia 63 0.401
13
P VSC011 Vasculitis 62 0.398
14
c FLL041 Follicular Lymphoma 1 49 0.395
15
RTC005 Reticulosarcoma 47 0.395
16
ATM095 Autoimmune Disease 62 0.394
17
PRP030 Purpura 54 0.393
18
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.373
19
P RHM011 Rheumatoid Arthritis 80 0.372
20
P THR014 Thrombocytopenia 67 0.340
21
c SYS001 Systemic Lupus Erythematosus 86 0.336
22
P NPH012 Nephrotic Syndrome 60 0.336
23
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.329
24
P LPS004 Lupus Erythematosus 61 0.329
25
DWN001 Down Syndrome 70 0.322
26
P PMP001 Pemphigus 54 0.315
27
MRG003 Marginal Zone B-Cell Lymphoma 52 0.305
28
P LYM033 Lymphoproliferative Syndrome 59 0.291
29
P ART022 Arthritis 69 0.290
30
MCR004 Macroglobulinemia 49 0.276
31
P HML002 Hemolytic Anemia 63 0.261
32
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.256
33
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.254
34
ANC002 Anca-Associated Vasculitis 41 0.251
35
GRN037 Granulomatosis with Polyangiitis 65 0.247
36
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.247
37
PMP006 Pemphigus Vulgaris, Familial 57 0.242
38
BRK010 Burkitt Lymphoma 67 0.239
39
PST046 Post-Transplant Lymphoproliferative Disease 53 0.237
40
P GLM007 Glomerulonephritis 57 0.233
41
c RHB024 Rhabdomyosarcoma 2 67 0.232
42
c ANM038 Anemia, Autoimmune Hemolytic 62 0.229
43
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.229
44
LYM012 Lymphoplasmacytic Lymphoma 47 0.226
45
P GRF003 Graft-Versus-Host Disease 72 0.223
46
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.223
47
P MMB011 Membranous Nephropathy 50 0.220
48
WLD007 Waldenstroem's Macroglobulinemia 61 0.219
49
P CNT005 Central Nervous System Lymphoma 53 0.217
50
LNG099 Lung Disease 60 0.208
51
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.206
52
FCT007 Factor Vii Deficiency 67 0.202
53
P NRP001 Neuropathy 56 0.202
54
c PRM226 Primary Central Nervous System Lymphoma 48 0.199
55
P MLT020 Multiple Sclerosis 72 0.197
56
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.195
57
DFC004 Deficiency Anemia 70 0.195
58
NRM001 Neuromyelitis Optica 61 0.195
59
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.194
60
P AGM001 Agammaglobulinemia 65 0.193
61
c HPT016 Hepatitis B 59 0.191
62
INT066 Interstitial Lung Disease 60 0.189
63
P MYS003 Myasthenia Gravis 68 0.188
64
CRY004 Cryoglobulinemia 48 0.185
65
P FCL005 Focal Segmental Glomerulosclerosis 57 0.184
66
MYL069 Myeloma, Multiple 85 0.180
67
P TRN020 Turner Syndrome 67 0.180
68
P LKM062 Leukemia, Acute Lymphoblastic 69 0.177
69
P EXN002 Exanthem 57 0.177
70
MCR088 Microscopic Polyangiitis 51 0.173
71
P KDN018 Kidney Disease 72 0.169
72
ADL002 Adult Syndrome 70 0.169
73
BLL006 Bullous Pemphigoid 62 0.168
74
END086 End Stage Renal Disease 51 0.168
75
CLL014 Cll/sll 45 0.168
76
PLS009 Plasma Cell Neoplasm 51 0.165
77
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.163
78
48X005 48,xyyy 39 0.162
79
SPL004 Splenic Marginal Zone Lymphoma 51 0.160
80
c SCL052 Scleroderma, Familial Progressive 61 0.153
81
LYM027 Lymphopenia 58 0.153
82
MYL009 Myelodysplastic Syndrome 70 0.152
83
LYM040 Lymphoblastic Lymphoma 54 0.152
84
ENT004 Enthesopathy 49 0.152
85
ATM052 Autoimmune Disease 1 37 0.152
86
c CHR417 Chronic Graft Versus Host Disease 57 0.151
87
P HPT021 Hepatitis 67 0.150
88
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.148
89
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.146
90
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.146
91
P PNM007 Pneumonia 68 0.145
92
P DRM010 Dermatomyositis 61 0.144
93
CYT002 Cytokine Deficiency 42 0.143
94
HRY003 Hairy Cell Leukemia 55 0.142
95
SPL018 Splenomegaly 48 0.142
96
c ACQ014 Acquired Hemophilia 45 0.142
97
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.141
98
P PRP019 Peripheral Nervous System Disease 58 0.139
99
IDP091 Idiopathic Nephrotic Syndrome 42 0.139
100
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.139
101
P ENC004 Encephalitis 61 0.138
102
P PLY019 Polyneuropathy 56 0.138
103
P SRC025 Sarcoidosis 1 70 0.137
104
P MYP004 Myopathy 70 0.136
105
P MYS005 Myositis 56 0.136
106
P ANT006 Antiphospholipid Syndrome 55 0.136
107
c HPT073 Hepatitis C Virus 72 0.135
108
ALL026 Allergic Hypersensitivity Disease 62 0.135
109
P HMP007 Hemophilia 51 0.135
110
IND005 Indolent B Cell Lymphoma 20 0.135
111
IND016 Indolent B-Cell Non-Hodgkin Lymphoma 34 0.132
112
HMT002 Hematologic Cancer 62 0.131
113
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.131
114
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.129
115
HML018 Homologous Wasting Disease 22 0.129
116
P PRR002 Pure Red-Cell Aplasia 47 0.128
117
RDC006 Red Cell Aplasia 43 0.128
118
P SJG008 Sjogren Syndrome 61 0.127
119
PLS025 Plasmablastic Lymphoma 47 0.127
120
P SYS005 Systemic Scleroderma 68 0.126
121
CHR001 Churg-Strauss Syndrome 61 0.126
122
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.124
123
CNN005 Connective Tissue Disease 68 0.123
124
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.123
125
IMM167 Immune Deficiency Disease 78 0.121
126
c ACT135 Acute Graft Versus Host Disease 52 0.121
127
CLD007 Cold Agglutinin Disease 45 0.121
128
c HPT001 Hepatitis C 62 0.120
129
P PLY041 Polymyositis 57 0.120
130
c HMP029 Hemophilia a 67 0.119
132
P RSP003 Respiratory Failure 74 0.116
133
NDL024 Nodal Marginal Zone Lymphoma 38 0.116
134
c SYS043 Systemic Lupus Erythematosus 1 38 0.116
135
OCL020 Ocular Cicatricial Pemphigoid 55 0.114
136
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.114
137
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.113
138
P GRV001 Graves' Disease 55 0.113
139
c CHR682 Chronic Bilirubin Encephalopathy 39 0.113
140
HDG004 Hodgkin's Granuloma 23 0.113
141
HDG006 Hodgkin's Paragranuloma 22 0.113
142
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.111
143
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.111
144
PMP004 Pemphigus Foliaceus 43 0.111
145
MMB001 Membranoproliferative Glomerulonephritis 55 0.110
146
LYM051 Lymphomatoid Granulomatosis 45 0.110
147
ATX019 Ataxia with Vitamin E Deficiency 42 0.110
148
KPS004 Kaposi Sarcoma 75 0.108
149
CST005 Castleman Disease 57 0.108
150
c LKM061 Leukemia, Acute Myeloid 84 0.107
151
P CNR004 Cone-Rod Dystrophy 2 73 0.107
152
ACQ007 Acquired Immunodeficiency Syndrome 60 0.107
153
P MYC033 Myoclonus 46 0.107
154
GLM044 Glomerular Disease 37 0.107
155
SKN016 Skin Disease 63 0.105
156
EVN001 Evans' Syndrome 48 0.105
157
P MYL006 Myeloid Leukemia 60 0.104
158
HRP004 Herpes Zoster 60 0.104
159
P SCL015 Scleritis 48 0.104
160
SVR004 Severe Combined Immunodeficiency 73 0.102
161
HMN044 Human Immunodeficiency Virus Type 1 71 0.102
163
47X002 47,xyy 49 0.102
164
PRL017 Prolymphocytic Leukemia 47 0.102
165
PRN049 Paraneoplastic Pemphigus 42 0.100
166
EXP004 Exophthalmos 52 0.099
167
MLT113 Multicentric Castleman Disease 47 0.099
168
TTN003 Tetanus 65 0.097
169
INT054 Intraocular Lymphoma 48 0.097
171
ALL012 Allergic Angiitis 24 0.097
172
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.095
173
MCS002 Mucositis 56 0.095
174
P HMN032 Human Herpesvirus 8 47 0.095
175
P PSR002 Psoriasis 62 0.093
176
TXC002 Toxic Encephalopathy 53 0.093
177
PST011 Pustulosis of Palm and Sole 52 0.093
178
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.093
179
P APL001 Aplastic Anemia 74 0.092
180
CMM004 Common Variable Immunodeficiency 68 0.092
181
P PLM036 Pulmonary Fibrosis 65 0.092
182
P ENC018 Encephalopathy 61 0.092
183
PNM001 Pneumocystosis 59 0.092
184
FRY002 Fryns Syndrome 43 0.092
185
THR123 Thrombotic Microangiopathy 36 0.092
186
LVR012 Liver Cirrhosis 62 0.090
187
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.090
188
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.090
189
c CHR684 Chronic Kidney Disease 70 0.088
190
SRC014 Sarcoma 65 0.088
191
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.088
192
P PRM006 Primary Biliary Cirrhosis 62 0.088
193
P URT039 Urticaria 58 0.088
194
EYD002 Eye Disease 58 0.088
195
P UVT001 Uveitis 57 0.088
196
BCT022 Bacterial Infectious Disease 56 0.088
197
P DRR001 Diarrhea 55 0.088
198
SPN035 Spindle Cell Sarcoma 53 0.088
199
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.088
200
P DMY001 Demyelinating Polyneuropathy 43 0.088
201
c ACQ042 Acquired Hemophilia a 37 0.088
202
CHC001 Chickenpox 60 0.086
203
c ACT071 Acute Kidney Failure 60 0.086
204
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.084
205
CHR066 Chronic Fatigue Syndrome 61 0.084
206
STF001 Stiff-Person Syndrome 60 0.084
207
PNC001 Pancytopenia 54 0.084
208
P EPD016 Epidermolysis Bullosa 53 0.084
209
DMY004 Demyelinating Disease 52 0.084
210
MYL001 Myelitis 51 0.084
211
EPD006 Epidermolysis Bullosa Acquisita 49 0.084
212
c NPH049 Nephrotic Syndrome, Type 2 48 0.084
213
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 40 0.084
214
CLT003 Colitis 62 0.082
215
GLS018 Glass Syndrome 57 0.082
216
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.082
217
PRP036 Peripheral T-Cell Lymphoma 53 0.082
218
c PRM163 Primary Mediastinal Large B-Cell Lymphoma 41 0.082
219
DFF031 Diffuse Alveolar Hemorrhage 30 0.082
220
c SPN225 Spondyloarthropathy 1 73 0.080
221
P OPT009 Optic Neuritis 57 0.080
222
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.080
223
NRT004 Neuritis 52 0.080
224
P THY032 Thyroiditis 52 0.080
225
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.080
226
c PRM108 Primary Progressive Multiple Sclerosis 51 0.080
227
ANT039 Antisynthetase Syndrome 46 0.080
228
DFF003 Diffuse Scleroderma 41 0.080
229
INT221 Intravascular Large B-Cell Lymphoma 35 0.080
230
P MNN013 Meningitis 66 0.078
231
c ACT073 Acute Leukemia 58 0.078
232
P ANP001 Anaplastic Large Cell Lymphoma 58 0.078
233
P CHL066 Cholangitis 51 0.078
234
P TRN034 Transverse Myelitis 45 0.078
235
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 30 0.078
236
c HYP595 Hypertension, Essential 84 0.075
237
P NRV007 Nervous System Disease 66 0.075
238
c ACT068 Acute Cystitis 63 0.075
239
BRN002 Bronchiolitis 59 0.075
240
CYT008 Cytomegalovirus Infection 57 0.075
241
SYN007 Synovitis 54 0.075
242
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.075
243
SPN051 Spondylitis 51 0.075
244
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.075
245
GRN017 Granulocytopenia 44 0.075
246
GST027 Gastric Lymphoma 44 0.075
247
P PRM293 Primary Mediastinal B-Cell Lymphoma 43 0.075
248
PLC002 Plica Syndrome 36 0.075
249
c PRM299 Primary Cutaneous B-Cell Lymphoma 35 0.075
250
RFR002 Refractory Hairy Cell Leukemia 33 0.075
251
INF009 Inflammatory Spondylopathy 31 0.075
252
ULC004 Ulcerative Colitis 73 0.073
253
c LKM063 Leukemia, Chronic Myeloid 72 0.073
254
CNS004 Constipation 58 0.073
255
P ANG015 Angioedema 57 0.073
256
BRN012 Bronchiolitis Obliterans 55 0.073
257
P ALP008 Alopecia 54 0.073
258
P HML001 Hemolytic-Uremic Syndrome 53 0.073
259
FCT001 Factor Viii Deficiency 51 0.073
260
MNN009 Meningoencephalitis 49 0.073
261
IGG001 Iga Glomerulonephritis 48 0.073
262
P LYM024 Lymphatic System Disease 48 0.073
263
RYN005 Raynaud Phenomenon 47 0.073
264
49X006 49, Xxxxy Syndrome 41 0.073
265
SYS071 Systemic Autoimmune Disease 37 0.073
266
c TYP024 Type Ii Mixed Cryoglobulinemia 34 0.073
267
ADR007 Adrenoleukodystrophy 75 0.071
268
P MYC007 Myocardial Infarction 70 0.071
269
c JVN010 Juvenile Rheumatoid Arthritis 64 0.071
270
TXC005 Toxic Shock Syndrome 62 0.071
271
DRM006 Dermatitis 61 0.071
272
c JVN061 Juvenile Arthritis 60 0.071
273
CHL028 Childhood Type Dermatomyositis 58 0.071
274
SFT003 Soft Tissue Sarcoma 56 0.071
275
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.071
276
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.071
277
ORB013 Orbital Disease 42 0.071
278
GST020 Gastric Antral Vascular Ectasia 41 0.071
279
P MLG074 Malignant Mesenchymoma 40 0.071
280
CRH001 Crohn's Disease 74 0.069
281
P MLN008 Melanoma 69 0.069
282
P HYP098 Hypereosinophilic Syndrome 67 0.069
283
IDP011 Idiopathic Interstitial Pneumonia 59 0.069
284
MXD005 Mixed Connective Tissue Disease 58 0.069
285
P HYP076 Hyperthyroidism 55 0.069
286
PYD001 Pyoderma Gangrenosum 54 0.069
287
FLT011 Felty Syndrome 52 0.069
288
PYD002 Pyoderma 50 0.069
289
LPD004 Lipoid Nephrosis 46 0.069
290
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.069
291
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.069
292
CLS052 Classic Hairy Cell Leukemia 27 0.069
293
P HRT032 Heart Disease 75 0.066
294
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.066
295
P AMY004 Amyloidosis 70 0.066
296
CNG034 Congestive Heart Failure 69 0.066
297
P PNC044 Pancreatitis 61 0.066
298
VRL011 Viral Infectious Disease 61 0.066
299
c ATM024 Autoimmune Pancreatitis 55 0.066
300
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.066
301
SNS003 Sensory Peripheral Neuropathy 54 0.066
302
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.066
303
P CTN015 Cutaneous T Cell Lymphoma 49 0.066
304
P PLY020 Polyradiculoneuropathy 48 0.066
305
RCH001 Richter's Syndrome 45 0.066
306
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.063
307
P NRB001 Neuroblastoma 72 0.063
308
MYC006 Mycosis Fungoides 66 0.063
309
c ATM011 Autoimmune Hepatitis 63 0.063
310
c ACT134 Acute Liver Failure 56 0.063
311
P SCL009 Sclerosing Cholangitis 48 0.063
312
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.063
313
IMM136 Immune System Disease 45 0.063
314
P HYP073 Hypersensitivity Reaction Type Iv Disease 44 0.063
315
P MYC084 Mycobacterium Tuberculosis 1 68 0.061
316
RCK004 Rickets 68 0.061
317
KRT019 Keratitis, Hereditary 65 0.061
318
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.061
319
HSH003 Hashimoto Thyroiditis 62 0.061
320
ISC004 Ischemia 58 0.061
321
DSS008 Disease of Mental Health 58 0.061
322
THR024 Thrombosis 57 0.061
323
P PLM006 Pulmonary Alveolar Proteinosis 53 0.061
324
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.061
325
CCT002 Cicatricial Pemphigoid 51 0.061
326
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.061
327
RTN001 Retinal Vasculitis 47 0.061
328
CRS001 Crescentic Glomerulonephritis 43 0.061
329
TRP009 Triple X Syndrome 42 0.061
330
RTR011 Retroperitoneal Fibrosis 40 0.061
331
c ATM075 Autoimmune Encephalitis 38 0.061
332
c LKM005 Leukemia, T-Cell, Chronic 34 0.061
333
c CHR064 Chronic Monocytic Leukemia 33 0.061
334
P ATM076 Autoimmune Retinopathy 27 0.061
335
P ASP006 Aspergillosis 69 0.058
336
P LVR013 Liver Disease 68 0.058
337
P HRP006 Herpes Simplex 65 0.058
338
PSR001 Psoriatic Arthritis 61 0.058
339
SZR001 Sezary's Disease 60 0.058
340
P MYC008 Myocarditis 59 0.058
341
P BRN022 Bronchiectasis 59 0.058
342
FNG017 Fungal Infectious Disease 53 0.058
343
P CTN003 Cutaneous Lupus Erythematosus 53 0.058
344
PNN001 Panniculitis 51 0.058
345
CLC006 Calcinosis 48 0.058
346
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.058
347
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.058
348
CVD001 Covid-19 44 0.058
349
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.058
350
MNN002 Mononeuritis Multiplex 41 0.058
351
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.058
352
C1N001 C1 Inhibitor Deficiency 39 0.058
353
CHR178 Chromosomal Triplication 35 0.058
354
HRP008 Herpes Simiae 25 0.058
355
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.055
356
P HYP086 Hypothyroidism 69 0.055
357
P INF038 Influenza 68 0.055
358
P DRM053 Dermatitis, Atopic 66 0.055
359
P THY023 Thymoma 65 0.055
360
P DBT009 Diabetes Mellitus 64 0.055
361
PRT036 Peritonitis 64 0.055
362
LPD008 Lipid Metabolism Disorder 62 0.055
363
TKY002 Takayasu Arteritis 62 0.055
364
MSL001 Measles 62 0.055
365
c ACT027 Acute Pancreatitis 60 0.055
366
P OPT006 Optic Nerve Disease 60 0.055
367
VSL002 Visual Epilepsy 59 0.055
368
INC002 Inclusion Body Myositis 58 0.055
369
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.055
370
ERY003 Erythema Multiforme 58 0.055
371
c CHL119 Cholangitis, Primary Sclerosing 57 0.055
372
DSS009 Disseminated Intravascular Coagulation 57 0.055
373
P ADL017 Adult T-Cell Leukemia 56 0.055
374
CMR002 Coumarin Resistance 56 0.055
375
P SZR006 Seizure Disorder 56 0.055
376
c THY107 Thymoma, Familial 52 0.055
377
TLN003 Telangiectasis 52 0.055
378
P SCK005 Sickle Cell Disease 50 0.055
379
DYS073 Dysphagia 50 0.055
380
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.055
381
P CLL015 Collagen Disease 47 0.055
382
LTH001 Lethal Midline Granuloma 44 0.055
383
PRS063 Paresthesia 41 0.055
384
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.055
385
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.055
386
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.055
387
ERY066 Erythema Multiforme Major 30 0.055
388
P LNG032 Lung Cancer 98 0.052
389
P GST053 Gastric Cancer 83 0.052
390
c THR092 Thrombophilia Due to Thrombin Defect 73 0.052
391
SVR097 Severe Cutaneous Adverse Reaction 69 0.052
392
BRN024 Bronchitis 68 0.052
393
c DBT099 Diabetes Mellitus, Type I 65 0.052
394
P VSC007 Vascular Disease 63 0.052
395
c FNC043 Fanconi Anemia, Complementation Group E 62 0.052
396
P DYS193 Dystonia 11, Myoclonic 55 0.052
397
P INF037 Inflammatory Bowel Disease 54 0.052
398
CLL003 Cellulitis 54 0.052
399
PLS016 Plasma Cell Leukemia 53 0.052
400
c CNT035 Central Nervous System Disease 52 0.052
401
c VRL010 Viral Hepatitis 52 0.052
402
c ACQ017 Acquired Von Willebrand Syndrome 49 0.052
403
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.052
404
SLD003 Sialadenitis 49 0.052
405
ACT029 Acute Interstitial Pneumonia 49 0.052
406
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.052
407
P PRL003 Proliferative Glomerulonephritis 44 0.052
408
P RRT020 Rare Tumor 41 0.052
409
c ACQ012 Acquired Angioedema 38 0.052
410
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.052
411
RHM014 Rheumatoid Vasculitis 37 0.052
413
TFR002 Tafro Syndrome 34 0.052
414
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.052
415
P CLR023 Colorectal Cancer 99 0.048
416
P PRS040 Prostate Cancer 97 0.048
417
P ATX030 Ataxia-Telangiectasia 82 0.048
418
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.048
419
AST005 Asthma 76 0.048
420
AGM019 Agammaglobulinemia, X-Linked 71 0.048
421
MYL005 Myelofibrosis 70 0.048
422
c BSL007 Basal Cell Carcinoma 68 0.048
423
SKN019 Skin Melanoma 68 0.048
424
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.048
425
PSY004 Psychotic Disorder 67 0.048
426
c MCL013 Mucolipidosis Iv 66 0.048
427
MRK001 Merkel Cell Carcinoma 65 0.048
428
P PRS038 Personality Disorder 65 0.048
429
c HPT003 Hepatitis a 62 0.048
430
P ART023 Arthropathy 62 0.048
431
P GLL022 Guillain-Barre Syndrome 59 0.048
432
P PLY017 Polyarteritis Nodosa 58 0.048
433
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.048
434
EXT034 Extrinsic Allergic Alveolitis 58 0.048
435
P RHN004 Rhinitis 57 0.048
436
P END033 Endocarditis 57 0.048
437
PLS011 Plasmacytoma 56 0.048
438
SCH003 Schizophreniform Disorder 56 0.048
439
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.048
440
P TRM003 Tremor 54 0.048
441
CRY001 Cryptogenic Organizing Pneumonia 53 0.048
442
KRT006 Keratoconjunctivitis 53 0.048
443
KRT001 Keratoconjunctivitis Sicca 49 0.048
444
CNT033 Central Nervous System Cancer 47 0.048
445
NNS002 Nonspecific Interstitial Pneumonia 45 0.048
446
BNM001 Bone Marrow Cancer 43 0.048
447
LMB024 Limbic Encephalitis 41 0.048
448
TST004 Testicular Lymphoma 39 0.048
449
CMP040 Complement Component 4, Partial Deficiency of 33 0.048
450
PRM129 Primary Cutaneous Marginal Zone B-Cell Lymphoma 30 0.048
451
ATM069 Autoimmune Hemolytic Anemia, Warm Type 28 0.048
452
P OVR096 Overlap Myositis 27 0.048
453
CHL079 Children's Interstitial Lung Disease 26 0.048
454
FBR085 Fibrillary Glomerulonephritis 24 0.048
455
CHR208 Chromosome 17p Deletion 23 0.048
456
WRM004 Warm Antibody Hemolytic Anemia 20 0.048
457
STR067 Stroke, Ischemic 81 0.045
458
ANX010 Anxiety 73 0.045
459
P SKN015 Skin Carcinoma 66 0.045
460
P CNJ013 Conjunctivitis 65 0.045
461
NTR005 Nutritional Deficiency Disease 62 0.045
462
HYP066 Hyperglycemia 61 0.045
463
DPH001 Diphtheria 60 0.045
464
SQM006 Squamous Cell Carcinoma 60 0.045
465
P CND004 Candidiasis 58 0.045
466
IRN002 Iron Metabolism Disease 57 0.045
467
P HDC001 Headache 57 0.045
468
ORL005 Oral Candidiasis 56 0.045
469
HNC001 Henoch-Schoenlein Purpura 55 0.045
470
ANL018 Analbuminemia 54 0.045
471
WST005 West Nile Virus 54 0.045
472
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.045
473
INF034 Infective Endocarditis 53 0.045
474
c MCR113 Microvascular Complications of Diabetes 3 52 0.045
475
FSC004 Fasciitis 50 0.045
476
RTN023 Retinitis 46 0.045
477
MLT075 Multifocal Motor Neuropathy 46 0.045
478
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.045
479
BCL002 B Cell Deficiency 43 0.045
480
OCL011 Ocular Motility Disease 42 0.045
481
NRR001 Neuroretinitis 42 0.045
482
LRG008 Large Granular Lymphocyte Leukemia 41 0.045
483
c THR037 Thrombocytopenia 2 40 0.045
484
P BCL005 B Cell Prolymphocytic Leukemia 39 0.045
485
CRB001 Cerebral Lymphoma 39 0.045
486
FBR089 Fibrosclerosis, Multifocal 38 0.045
487
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.045
488
ORB008 Orbital Plasma Cell Granuloma 31 0.045
489
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.045
490
BRW002 Brown's Tendon Sheath Syndrome 28 0.045
491
FTL073 Fetal Anticonvulsant Syndrome 26 0.045
492
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.045
493
PRM128 Primary Cutaneous Follicle Center Lymphoma 25 0.045
494
IMM053 Immunotactoid Glomerulopathy 25 0.045
496
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.041
497
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.041
498
c ATR087 Atrial Standstill 1 75 0.041
499
SCK003 Sickle Cell Anemia 74 0.041
500
P SCH015 Schizophrenia 74 0.041
501
OTT002 Otitis Media 72 0.041
502
c GLY008 Glycogen Storage Disease Ii 70 0.041
503
P DMN001 Diamond-Blackfan Anemia 69 0.041
504
P OCL013 Oculodentodigital Dysplasia 69 0.041
505
OBS002 Obsessive-Compulsive Disorder 68 0.041
506
CRB039 Cerebrovascular Disease 67 0.041
507
P PLM037 Pulmonary Hypertension 67 0.041
508
P DMN002 Dementia 66 0.041
509
HYP056 Hypoglycemia 66 0.041
510
MYL031 Myeloproliferative Neoplasm 66 0.041
511
KHL003 Kohlschutter-Tonz Syndrome 65 0.041
512
P ADL010 Adult Respiratory Distress Syndrome 65 0.041
513
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.041
514
c LCL006 Localized Scleroderma 62 0.041
515
c BRN108 Branchiootic Syndrome 1 62 0.041
516
OST003 Osteonecrosis 61 0.041
517
P CHR285 Chronic Myelomonocytic Leukemia 60 0.041
518
PRT058 Pure Autonomic Failure 59 0.041
519
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.041
520
ADL030 Adult-Onset Still's Disease 58 0.041
521
AGN016 Aging 56 0.041
522
P GST044 Gastritis 56 0.041
523
HYP005 Hypokalemia 55 0.041
524
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.041
525
P STR020 Strabismus 55 0.041
526
LMB002 Lambert-Eaton Myasthenic Syndrome 53 0.041
527
GTR002 Goiter 53 0.041
528
JCB001 Jacobsen Syndrome 52 0.041
529
ASP003 Aseptic Meningitis 51 0.041
530
INT071 Intestinal Perforation 51 0.041
531
STM007 Stomatitis 50 0.041
532
P IGN003 Iga Nephropathy 1 49 0.041
533
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.041
534
HST010 Histiocytosis 48 0.041
535
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.041
536
ESN015 Eosinophilic Fasciitis 48 0.041
537
OBS003 Obsessive-Compulsive Personality Disorder 46 0.041
538
MYX004 Myxedema 43 0.041
539
MCH006 Mechanical Strabismus 42 0.041
540
LYM116 Lymph Node Disease 41 0.041
541
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.041
542
HYP344 Hyperthyroidism, Familial Gestational 39 0.041
543
P BNL002 Bone Lymphoma 34 0.041
544
ORB009 Orbit Lymphoma 33 0.041
545
c THR110 Thrombocytopenia 6 28 0.041
546
c BKV001 Bk-Virus Nephropathy 24 0.041
547
ORB020 Orbital Lymphoma 23 0.041
548
ATM074 Autoimmune Autonomic Ganglionopathy 22 0.041
550
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 19 0.041
551
P BRS047 Breast Cancer 97 0.037
552
BRN028 Brain Cancer 74 0.037
553
MLT157 Multiple System Atrophy 1 70 0.037
554
c HMP004 Hemophilia B 68 0.037
555
c INF071 Inflammatory Bowel Disease 1 67 0.037
556
KRN002 Kearns-Sayre Syndrome 63 0.037
557
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.037
558
MDD011 Mood Disorder 62 0.037
559
P HYP097 Hyperekplexia 61 0.037
560
P KDN017 Kidney Cancer 60 0.037
561
P ALP009 Alopecia Areata 60 0.037
562
PMS001 Poems Syndrome 60 0.037
563
P GLY013 Glycogen Storage Disease 60 0.037
564
P THL005 Thalassemia 60 0.037
565
THY029 Thyroid Carcinoma 59 0.037
566
PLM033 Pulmonary Embolism 59 0.037
567
P CYS018 Cystitis 59 0.037
568
GNG013 Gingivitis 59 0.037
569
SPT004 Septic Arthritis 58 0.037
570
LNG108 Langerhans Cell Histiocytosis 58 0.037
571
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.037
572
c ACT075 Acute Myocardial Infarction 57 0.037
573
APH002 Aphasia 57 0.037
574
P PYL005 Pyelonephritis 56 0.037
575
GDP001 Goodpasture Syndrome 55 0.037
576
ATR057 Atrioventricular Block 55 0.037
577
c FML035 Familial Hyperlipidemia 55 0.037
578
PLM012 Pulmonary Sarcoidosis 53 0.037
579
P LCH002 Lichen Planus 53 0.037
580
c DMN023 Diamond-Blackfan Anemia 1 53 0.037
581
CRH005 Crohn's Colitis 53 0.037
582
IRD001 Iridocyclitis 53 0.037
583
GST023 Gastric Ulcer 53 0.037
584
c HPT007 Hepatitis E 53 0.037
585
SCH002 Schnitzler Syndrome 52 0.037
586
ILS001 Ileus 51 0.037
587
ACT049 Acute Disseminated Encephalomyelitis 51 0.037
588
P PRC012 Pericardial Effusion 51 0.037
589
CYT005 Cytomegalovirus Retinitis 50 0.037
590
PRN009 Paranoid Schizophrenia 50 0.037
591
HMG002 Hemoglobinuria 50 0.037
592
c CHR418 Chronic Leukemia 49 0.037
593
HMP001 Hemopericardium 48 0.037
594
DRY001 Dry Eye Syndrome 47 0.037
595
c MCR120 Microvascular Complications of Diabetes 7 47 0.037
596
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.037
597
PDT035 Pediatric Systemic Lupus Erythematosus 46 0.037
598
HMR023 Hemorrhagic Cystitis 45 0.037
599
C3G002 C3 Glomerulopathy 45 0.037
600
ART012 Aortitis 44 0.037
601
TNS014 Tenosynovitis 44 0.037
602
c HYP699 Hyperekplexia 1 44 0.037
603
HSD004 Hsd10 Mitochondrial Disease 44 0.037
604
FLL013 Follicular Dendritic Cell Sarcoma 43 0.037
605
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.037
606
c MCR130 Microvascular Complications of Diabetes 6 41 0.037
607
c MCR133 Microvascular Complications of Diabetes 4 41 0.037
608
SPR126 Superior Semicircular Canal Dehiscence 40 0.037
609
IMM001 Immune-Complex Glomerulonephritis 40 0.037
610
c HMG029 Hemoglobin Se Disease 39 0.037
611
HRT040 Hirata Disease 38 0.037
612
NRS005 Neurosarcoidosis 36 0.037
613
LNG013 Lung Lymphoma 35 0.037
614
GRY001 Gray Zone Lymphoma 35 0.037
615
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.037
616
c ADL001 Adult Lymphoma 34 0.037
617
c THR102 Thrombocytopenia 5 30 0.037
618
MLT105 Multiple System Atrophy, Cerebellar Type 29 0.037
619
PMP008 Pemphigus Vegetans 27 0.037
620
LVR006 Liver Lymphoma 27 0.037
621
c ACQ016 Acquired Pure Red Cell Aplasia 27 0.037
622
NCR015 Necrotizing Autoimmune Myopathy 26 0.037
623
c RRH015 Rare Hemorrhagic Disorder 23 0.037
624
CTN020 Cutaneous Sclerosis 17 0.037
626
P PNC035 Pancreatic Cancer 84 0.032
627
P GLM040 Glioma Susceptibility 1 81 0.032
628
PFF001 Pfeiffer Syndrome 79 0.032
629
P LNG064 Lung Cancer Susceptibility 3 78 0.032
630
GLB015 Glioblastoma Multiforme 75 0.032
631
P OST002 Osteoporosis 74 0.032
632
c BTT014 Beta-Thalassemia 74 0.032
633
c MNN043 Meningioma, Familial 74 0.032
634
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.032
635
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.032
636
P WSK001 Wiskott-Aldrich Syndrome 72 0.032
637
BHC003 Behcet Syndrome 71 0.032
638
P EPL164 Epilepsy 71 0.032
639
CRT072 Creutzfeldt-Jakob Disease 70 0.032
640
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.032
641
P CLC063 Celiac Disease 1 66 0.032
642
c SML038 Small Cell Cancer of the Lung 65 0.032
643
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.032
644
PND002 Pendred Syndrome 65 0.032
645
NRM005 Neuromuscular Disease 64 0.032
646
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.032
647
MSC007 Muscle Hypertrophy 64 0.032
648
P ADN016 Adenocarcinoma 64 0.032
649
OST017 Osteomyelitis 64 0.032
650
P CRN300 Coronary Heart Disease 1 63 0.032
651
c ALP101 Alpha-Thalassemia 62 0.032
652
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.032
653
LPP008 Lipoprotein Quantitative Trait Locus 62 0.032
654
MNN042 Meningioma, Radiation-Induced 62 0.032
655
CHL068 Cholestasis 61 0.032
656
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.032
657
CRD223 Cardiac Arrhythmia 60 0.032
658
P SNS001 Sensorineural Hearing Loss 60 0.032
659
P CTR002 Cataract 60 0.032
660
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.032
661
STT001 Status Epilepticus 60 0.032
662
P BND020 Bone Disease 59 0.032
663
GST045 Gastroenteritis 59 0.032
664
HLC007 Helicobacter Pylori Infection 59 0.032
665
CRY005 Cryptococcosis 58 0.032
666
CRD132 Cardiac Conduction Defect 58 0.032
667
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 57 0.032
668
P CRD246 Cardiovascular System Disease 57 0.032
669
HYP266 Hypoxia 57 0.032
670
PNM008 Pneumothorax 56 0.032
671
c BSL024 Basal Cell Carcinoma 1 56 0.032
672
EXF001 Exfoliation Syndrome 56 0.032
673
HMG005 Hemoglobinopathy 56 0.032
674
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.032
675
c NPH055 Nephrotic Syndrome, Type 1 56 0.032
676
VGT001 Vogt-Koyanagi-Harada Disease 55 0.032
677
CPL003 Capillary Leak Syndrome 55 0.032
678
OCL009 Ocular Cancer 55 0.032
679
CRT017 Cartilage Disease 54 0.032
680
GLC003 Glucose Intolerance 54 0.032
681
NCR004 Nocardiosis 54 0.032
682
PRC013 Pericarditis 54 0.032
683
PLM010 Pulmonary Edema 54 0.032
684
HMS001 Hemosiderosis 54 0.032
685
HRT012 Heart Valve Disease 53 0.032
686
HYP063 Hypersplenism 53 0.032
687
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.032
688
c PSR017 Psoriasis 2 53 0.032
689
P RTN018 Retinal Disease 53 0.032
690
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.032
691
ART140 Arteries, Anomalies of 52 0.032
692
THY030 Thyroid Gland Disease 52 0.032
693
P MSC003 Muscular Atrophy 52 0.032
694
c PSR023 Psoriasis 1 52 0.032
695
RYS001 Reye Syndrome 51 0.032
696
LNG031 Lung Benign Neoplasm 51 0.032
697
HYP081 Hypolipoproteinemia 51 0.032
698
CHR005 Chorioamnionitis 51 0.032
699
SPN021 Spinal Meningioma 50 0.032
700
c AMY009 Amyloidosis Aa 50 0.032
701
HYP017 Hypophosphatemia 50 0.032
702
P MST002 Mast-Cell Leukemia 49 0.032
703
MYL003 Myeloid Sarcoma 49 0.032
704
ATS010 Autosomal Recessive Disease 48 0.032
705
P NGH001 Night Blindness 48 0.032
706
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.032
707
P RNL015 Renal Hypertension 47 0.032
708
c PSR032 Psoriasis 11 47 0.032
709
RNL077 Renal Fibrosis 47 0.032
710
CRD137 Cardiogenic Shock 47 0.032
711
CHR492 Chromosome 13q14 Deletion Syndrome 46 0.032
712
FCL012 Facial Paralysis 46 0.032
713
CLN045 Colonic Benign Neoplasm 46 0.032
714
KRT013 Keratolytic Winter Erythema 46 0.032
715
TCL003 T Cell Deficiency 46 0.032
716
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.032
717
c NPH054 Nephrotic Syndrome, Type 3 45 0.032
718
P DCR003 Dacryoadenitis 45 0.032
719
c DRM054 Dermatitis, Atopic, 2 44 0.032
720
SBC016 Subacute Delirium 44 0.032
721
SPN369 Spinal Disease 43 0.032
722
NSP002 Nasopharyngitis 43 0.032
723
c SRC023 Sarcoidosis 2 43 0.032
724
HMP009 Haemophilus Influenzae 43 0.032
725
c PSR028 Psoriasis 7 42 0.032
726
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.032
727
CHR286 Chronic Neutrophilic Leukemia 42 0.032
728
BCK006 Back Pain 42 0.032
729
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.032
730
MDS018 Mediastinal Cancer 41 0.032
731
c PSR018 Psoriasis 13 41 0.032
732
SCR001 Secretory Meningioma 41 0.032
733
MNT303 Mental Retardation, X-Linked, Syndromic, Cabezas Type 41 0.032
734
THR035 Thrombasthenia 40 0.032
735
OST115 Osteonecrosis of the Jaw 40 0.032
736
LNR006 Linear Iga Disease 40 0.032
737
PMP002 Pemphigoid Gestationis 39 0.032
738
c THR111 Thrombocytopenia 3 38 0.032
739
c ACT159 Acute Transverse Myelitis 38 0.032
740
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.032
741
P CRB059 Cerebellar Degeneration 37 0.032
742
DNS007 Dense Deposit Disease 37 0.032
743
PDT025 Pediatric Multiple Sclerosis 36 0.032
744
BRS001 Breast Lymphoma 36 0.032
745
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.032
746
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.032
747
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.032
748
GST014 Gastrointestinal Lymphoma 34 0.032
749
c ATM089 Autoimmune Neuropathy 34 0.032
750
MYC078 Myoclonus and Ataxia 33 0.032
751
c PRM039 Primary Angiitis of the Central Nervous System 33 0.032
752
c CHL157 Childhood B-Cell Acute Lymphoblastic Leukemia 33 0.032
753
c PRS136 Prostate Cancer, Hereditary, 6 33 0.032
754
c PRS130 Prostate Cancer, Hereditary, 8 32 0.032
755
WST010 West Nile Virus Infection 32 0.032
756
LYM043 Lymphocytic Hypophysitis 32 0.032
757
MRK002 Marek Disease 32 0.032
758
MDS019 Mediastinal Malignant Lymphoma 30 0.032
759
PCM002 Pauci-Immune Glomerulonephritis 30 0.032
760
c PST008 Posterior Scleritis 30 0.032
761
c CHR094 Chronic Polyneuropathy 29 0.032
762
CRD220 Cardiac Valvular Defect, Developmental 29 0.032
763
SYN092 Syndromic X-Linked Intellectual Disability Cabezas Type 28 0.032
764
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.032
765
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 27 0.032
767
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.032
768
MYC001 Myoclonic Cerebellar Dyssynergia 25 0.032
769
JVN026 Jeavons Syndrome 24 0.032
770
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 21 0.032
771
MXD035 Mixed-Type Autoimmune Hemolytic Anemia 21 0.032
772
PMP013 Pemphigus Gestationis 19 0.032
773
ORB010 Orbital Granuloma 19 0.032
774
c DRM058 Dermatitis, Atopic, 6 18 0.032
775
JVN060 Juvenile Idiopathic Inflammatory Myopathy 17 0.032
776
c BSL027 Basal Cell Carcinoma 4 16 0.032
777
KSH003 Kshv Inflammatory Cytokine Syndrome 16 0.032
778
PRP106 Peripheral Neuropathy Associated with Monoclonal Gammopathy 11 0.032
779
P OVR042 Ovarian Cancer 88 0.026
780
c FNC027 Fanconi Anemia, Complementation Group a 81 0.026
781
c NRF023 Neurofibromatosis, Type Ii 80 0.026
782
c DLT002 Dilated Cardiomyopathy 79 0.026
783
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.026
784
LPT014 Leptin Deficiency or Dysfunction 74 0.026
785
P NJM001 Nijmegen Breakage Syndrome 74 0.026
786
c HYP836 Hypercholesterolemia, Familial, 1 73 0.026
787
SCH036 Scheie Syndrome 72 0.026
788
PRP027 Peripheral Vascular Disease 71 0.026
789
SMT004 Smith-Lemli-Opitz Syndrome 70 0.026
790
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.026
791
P TMP003 Temporal Arteritis 68 0.026
792
PNC129 Pancreatic Adenocarcinoma 68 0.026
793
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.026
794
P KBK002 Kabuki Syndrome 1 67 0.026
795
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.026
796
BLM001 Bloom Syndrome 67 0.026
797
P CHR012 Chronic Granulomatous Disease 67 0.026
798
P MSC005 Muscular Dystrophy 66 0.026
799
GLN010 Glanzmann Thrombasthenia 66 0.026
800
P HYD006 Hydrocephalus 66 0.026
801
P VNW001 Von Willebrand's Disease 65 0.026
802
HRL003 Hurler Syndrome 65 0.026
803
ATH013 Atherosclerosis Susceptibility 65 0.026
804
BRC012 Brucellosis 64 0.026
805
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.026
806
RBR001 Roberts Syndrome 64 0.026
807
P GLM045 Glioma 63 0.026
808
P MVM001 Movement Disease 63 0.026
809
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.026
810
DPR016 Depression 63 0.026
811
c GM1007 Gm1 Gangliosidosis 62 0.026
812
c SVR001 Severe Acute Respiratory Syndrome 62 0.026
813
P ESP024 Esophagitis 62 0.026
814
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.026
815
RTN017 Retinal Detachment 61 0.026
816
P TXP001 Toxoplasmosis 60 0.026
817
HYD002 Hydronephrosis 60 0.026
818
P RBL001 Rubella 59 0.026
819
P BRS044 Breast Adenocarcinoma 59 0.026
820
HYP458 Hyper Ige Syndrome 58 0.026
821
P MMP001 Mumps 58 0.026
822
MNT002 Mental Depression 58 0.026
823
c DWL002 Dowling-Degos Disease 1 58 0.026
824
c LYS019 Loeys-Dietz Syndrome 1 57 0.026
825
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.026
826
BLR008 Bilirubin Metabolic Disorder 57 0.026
827
c GM1004 Gm1-Gangliosidosis, Type I 57 0.026
828
TCK001 Tick-Borne Encephalitis 56 0.026
829
HPT046 Hepatic Veno-Occlusive Disease 56 0.026
830
ALL006 Allergic Asthma 56 0.026
831
GST050 Gastrointestinal System Disease 56 0.026
832
SML019 Smallpox 56 0.026
833
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.026
834
HST011 Histoplasmosis 55 0.026
835
ORP003 Oropharynx Cancer 55 0.026
836
MCL006 Macular Retinal Edema 55 0.026
837
c BCT007 Bacterial Meningitis 55 0.026
838
P PLM034 Pulmonary Emphysema 55 0.026
839
HDR002 Hidradenitis Suppurativa 55 0.026
840
P DBT005 Diabetes Insipidus 55 0.026
841
P DRM007 Dermatitis Herpetiformis 55 0.026
842
HMP005 Hemiplegia 55 0.026
843
P SPN052 Spondyloarthropathy 54 0.026
844
RLP001 Relapsing Polychondritis 54 0.026
845
P ART021 Arteriosclerosis 54 0.026
846
c PST005 Posterior Uveitis 54 0.026
847
NNL006 Non-Alcoholic Steatohepatitis 54 0.026
848
P HYP083 Hypopituitarism 53 0.026
849
P HMR003 Hemorrhagic Disease 53 0.026
850
LYS002 Lysosomal Storage Disease 52 0.026
851
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.026
852
RSS025 Ras-Associated Autoimmune Leukoproliferative Disorder 52 0.026
853
P NRC002 Narcolepsy 52 0.026
854
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.026
855
PTH003 Pathologic Nystagmus 52 0.026
856
HYP014 Hyperuricemia 52 0.026
857
APR001 Apraxia 52 0.026
858
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.026
859
c VRL005 Viral Pneumonia 52 0.026
860
LYM004 Lymphoid Interstitial Pneumonia 51 0.026
861
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.026
862
P SPP010 Suppressor of Tumorigenicity 3 51 0.026
863
LNG095 Lung Abscess 51 0.026
864
ENT011 Enterocolitis 51 0.026
865
CYS036 Cystinosis, Nephropathic 51 0.026
866
P RNL007 Renal Tubular Acidosis 51 0.026
867
RSD004 Rosai-Dorfman Disease 51 0.026
868
ACT017 Acute Chest Syndrome 51 0.026
869
c ALM001 Al Amyloidosis 50 0.026
870
PLR007 Pleural Empyema 50 0.026
871
P FNC004 Fanconi Syndrome 50 0.026
872
P PNV001 Panuveitis 50 0.026
873
BLR001 Biliary Atresia 50 0.026
874
ATY042 Atypical Chronic Myeloid Leukemia 49 0.026
875
PPL021 Papilledema 49 0.026
876
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.026
877
HDR003 Hidradenitis 49 0.026
878
c INV001 Invasive Aspergillosis 49 0.026
879
VCC001 Vaccinia 49 0.026
880
CGN006 Cogan Syndrome 48 0.026
881
RYN001 Raynaud Disease 48 0.026
882
c BCT013 Bacterial Pneumonia 48 0.026
883
CRY014 Cryptococcal Meningitis 48 0.026
884
ASP007 Aspiration Pneumonia 48 0.026
885
CHR563 Chronic Eosinophilic Leukemia 48 0.026
886
INT067 Interstitial Nephritis 48 0.026
887
GNG008 Ganglioneuroblastoma 48 0.026
888
BBS001 Babesiosis 48 0.026
889
BNN003 Bone Inflammation Disease 48 0.026
890
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.026
891
HPR003 Heparin-Induced Thrombocytopenia 48 0.026
892
NRN001 Neuroendocrine Carcinoma 47 0.026
893
LMT001 Limited Scleroderma 47 0.026
894
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.026
895
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.026
896
P RTN014 Retinal Artery Occlusion 47 0.026
897
SPL012 Splenic Disease 47 0.026
898
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.026
899
P LPM005 Lipomatosis 46 0.026
900
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.026
901
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.026
902
CRN019 Coronary Artery Vasospasm 46 0.026
903
ANR004 Anuria 46 0.026
904
GLL048 Glial Tumor 45 0.026
905
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.026
906
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.026
907
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.026
908
ACT003 Acute Kidney Tubular Necrosis 45 0.026
909
CNT046 Central Nervous System Vasculitis 44 0.026
910
MCR225 Macrophage Activation Syndrome 44 0.026
911
P GNG009 Gangliosidosis 44 0.026
912
BCT021 Bacterial Sepsis 44 0.026
913
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.026
914
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.026
915
c ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 44 0.026
916
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.026
917
MXD050 Mixed Phenotype Acute Leukemia 43 0.026
918
ILC002 Ileocolitis 43 0.026
919
VRL003 Variola Major 42 0.026
920
THY009 Thyroid Lymphoma 42 0.026
921
P RRH023 Rare Hereditary Hemochromatosis 41 0.026
922
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.026
923
DND018 Dendritic Cell Tumor 40 0.026
924
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 40 0.026
925
BRN026 Branch Retinal Artery Occlusion 40 0.026
926
c HMG001 Hemoglobin C Disease 40 0.026
927
P FNC034 Fanconi Renotubular Syndrome 2 40 0.026
928
PYR004 Pyuria 40 0.026
929
ANG049 Angioedema Induced by Ace Inhibitors 40 0.026
930
c GLL037 Guillain-Barre Syndrome, Familial 39 0.026
931
P DYS021 Dysautonomia 39 0.026
932
ALL014 Allergic Encephalomyelitis 38 0.026
933
P FML355 Familial Intrahepatic Cholestasis 38 0.026
934
SPS019 Spastic Paraparesis 38 0.026
935
CDQ001 Cauda Equina Syndrome 38 0.026
936
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.026
937
CMP001 Composite Lymphoma 37 0.026
938
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 37 0.026
939
c ATM104 Autoimmune Vasculitis 37 0.026
940
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.026
941
CFH006 Cfhr5 Deficiency 37 0.026
942
DYS016 Dysgammaglobulinemia 36 0.026
943
c ATM045 Autoimmune Glomerulonephritis 36 0.026
944
LVD003 Livedoid Vasculitis 36 0.026
945
c DRM040 Dermatitis Herpetiformis, Familial 35 0.026
946
EPD005 Epidural Abscess 35 0.026
947
RFR013 Refractory Celiac Disease 35 0.026
948
PDT001 Pediatric Lymphoma 35 0.026
949
CNC014 Cancer-Associated Retinopathy 34 0.026
950
P HVY001 Heavy Chain Disease 34 0.026
951
FTD001 Foot Drop 33 0.026
952
LGP001 Lagophthalmos 30 0.026
953
RFR004 Refractory Hematologic Cancer 30 0.026
954
HDG005 Hodgkin's Lymphoma, Mixed Cellularity 30 0.026
955
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 29 0.026
956
c ANT023 Anterior Scleritis 29 0.026
957
PRS002 Prostate Lymphoma 29 0.026
958
PRX008 Paroxysmal Cold Hemoglobinuria 29 0.026
959
PRN032 Paraneoplastic Cerebellar Degeneration 28 0.026
960
BLD028 Bladder Lymphoma 27 0.026
961
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.026
962
UNC014 Unicentric Castleman Disease 26 0.026
963
BNM005 Bone Marrow Necrosis 25 0.026
964
MDS006 Mediastinal Gray Zone Lymphoma 24 0.026
965
CHR043 Chronic Inflammatory Demyelinating Polyneuritis 23 0.026
966
P C1Q005 C1q Nephropathy 22 0.026
967
LYM053 Lymphomatous Thyroiditis 22 0.026
968
PRN068 Paraneoplastic Limbic Encephalitis 21 0.026
969
LPS019 Lupus Erythematosus Tumidus 20 0.026
970
CD4008 Cd4/cd8 T-Cell Ratio 20 0.026
971
c CHR686 Chronic Cutaneous Lupus Erythematosus 19 0.026
972
c AHM002 Ah Amyloidosis 18 0.026
973
LPS018 Lupus Erythematosus Panniculitis 18 0.026
974
EPS047 Epstein-Barr Virus-Associated Malignant Lymphoproliferative Disorder 18 0.026
976
EPS031 Epstein-Barr Virus-Positive Diffuse Large B-Cell Lymphoma of the Elderly 15 0.026
977
P HPT023 Hepatocellular Carcinoma 100 0.018
978
ESP021 Esophageal Cancer 90 0.018
979
CYS001 Cystic Fibrosis 81 0.018
980
GST019 Gastrointestinal Stromal Tumor 78 0.018
981
CRV035 Cervical Cancer 76 0.018
982
P FML018 Familial Mediterranean Fever 73 0.018
983
P RTN024 Retinoblastoma 73 0.018
984
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.018
985
P MTC003 Metachromatic Leukodystrophy 70 0.018
986
c GCH015 Gaucher Disease, Type I 70 0.018
987
P OST001 Osteopetrosis 70 0.018
988
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.018
989
P KRB001 Krabbe Disease 69 0.018
990
PLY001 Polycythemia Vera 69 0.018
991
ACR008 Acrocallosal Syndrome 69 0.018
992
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.018
993
P ESS003 Essential Thrombocythemia 68 0.018
994
MLD001 Melioidosis 68 0.018
995
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.018
996
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.018
997
GST092 Gastroesophageal Reflux 67 0.018
998
P CRD119 Cardiac Arrest 67 0.018
999
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.018
1000
P DYS007 Dyskeratosis Congenita 67 0.018
1001
ALL003 Allergic Rhinitis 67 0.018
1002
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.018
1003
ANG054 Angina Pectoris 66 0.018
1004
CHD001 Chediak-Higashi Syndrome 66 0.018
1005
P MCR115 Microvascular Complications of Diabetes 5 66 0.018
1006
P CNG001 Congenital Myasthenic Syndrome 66 0.018
1007
c MCR129 Microvascular Complications of Diabetes 1 66 0.018
1008
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 0.018
1009
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.018
1010
ACR006 Aceruloplasminemia 65 0.018
1011
PRT037 Pertussis 65 0.018
1012
c WLM013 Wilms Tumor 1 65 0.018
1013
KWS002 Kawasaki Disease 65 0.018
1014
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.018
1015
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.018
1016
PLM031 Poliomyelitis 64 0.018
1017
LYM017 Lyme Disease 64 0.018
1018
RFS006 Refsum Disease, Classic 64 0.018
1019
MGK001 Megakaryocytic Leukemia 64 0.018
1020
P RHB003 Rhabdomyosarcoma 63 0.018
1021
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.018
1022
LSH001 Leishmaniasis 63 0.018
1023
P GCH001 Gaucher's Disease 63 0.018
1024
c PRC016 Pre-Eclampsia 63 0.018
1025
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.018
1026
HYP780 Hypoadrenocorticism, Familial 63 0.018
1027
P LMY004 Leiomyosarcoma 63 0.018
1028
BDD001 Budd-Chiari Syndrome 63 0.018
1029
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.018
1030
P ECT006 Ectodermal Dysplasia 62 0.018
1031
P PLY014 Polycystic Kidney Disease 62 0.018
1032
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.018
1033
P HYP750 Hypertriglyceridemia, Familial 62 0.018
1034
P ORT004 Orthostatic Intolerance 62 0.018
1035
P PRM002 Primary Hyperoxaluria 62 0.018
1036
ASP002 Aspartylglucosaminuria 62 0.018
1037
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.018
1038
FCS002 Fucosidosis 61 0.018
1039
c WLM018 Wilms Tumor 5 61 0.018
1040
APP008 Appendicitis 61 0.018
1041
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.018
1042
SPN186 Spinal Cord Injury 60 0.018
1043
RGH009 Right Atrial Isomerism 60 0.018
1044
P TST021 Testicular Germ Cell Tumor 60 0.018
1045
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.018
1046
ACN002 Acanthosis Nigricans 60 0.018
1047
RHM001 Rheumatic Fever 60 0.018
1048
VRC005 Varicose Veins 60 0.018
1049
INS001 Insulinoma 60 0.018
1050
VGN017 Vaginal Cancer 60 0.018
1051
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.018
1052
PRT013 Portal Hypertension 59 0.018
1053
CRT002 Cartilage-Hair Hypoplasia 59 0.018
1054
P MCR010 Microcephaly 59 0.018
1055
P LKD001 Leukodystrophy 59 0.018
1056
IGR001 Ige Responsiveness, Atopic 59 0.018
1057
P SLP005 Sleep Disorder 59 0.018
1058
GRD007 Grade Iii Astrocytoma 59 0.018
1059
ADN018 Adenoma 59 0.018
1060
P NPH005 Nephronophthisis 59 0.018
1061
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 59 0.018
1062
c SVR003 Severe Congenital Neutropenia 59 0.018
1063
FBR047 Fibromyalgia 58 0.018
1064
CHL067 Cholecystitis 57 0.018
1065
P ZLL001 Zellweger Syndrome 57 0.018
1066
APH001 Aphthous Stomatitis 57 0.018
1067
PHR003 Pharyngitis 57 0.018
1068
AYM001 Ayme-Gripp Syndrome 57 0.018
1069
PGM001 Pigmented Villonodular Synovitis 56 0.018
1070
P PLY018 Polycythemia 56 0.018
1071
LST001 Listeriosis 56 0.018
1072
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.018
1073
c INT072 Intestinal Pseudo-Obstruction 56 0.018
1074
PRS047 Prostatitis 56 0.018
1075
SBC001 Subacute Sclerosing Panencephalitis 56 0.018