Search results for Mycophenolate mofetil

969 hits were found for Mycophenolate mofetil

# Family MCID Name MIFTS Score
1
MYC060 Mycophenolate Mofetil Embryopathy 19 4.213
2
c SYS001 Systemic Lupus Erythematosus 87 0.624
3
P GRF003 Graft-Versus-Host Disease 72 0.613
4
P LPS004 Lupus Erythematosus 61 0.552
5
P LKM002 Leukemia 67 0.453
6
P LYM118 Lymphoma 69 0.422
7
c ACT135 Acute Graft Versus Host Disease 52 0.420
8
LYM019 Lymphosarcoma 47 0.413
9
P KDN018 Kidney Disease 71 0.407
10
P MYL006 Myeloid Leukemia 60 0.403
11
MYL009 Myelodysplastic Syndrome 71 0.400
12
P LYM031 Lymphocytic Leukemia 55 0.381
13
P NTR004 Neutropenia 63 0.374
14
c LKM061 Leukemia, Acute Myeloid 83 0.369
15
P LKM062 Leukemia, Acute Lymphoblastic 69 0.357
16
P GLM007 Glomerulonephritis 57 0.351
17
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.350
18
ATM095 Autoimmune Disease 61 0.343
19
P NPH012 Nephrotic Syndrome 63 0.340
20
HMT002 Hematologic Cancer 62 0.338
21
LYM040 Lymphoblastic Lymphoma 54 0.337
22
HML018 Homologous Wasting Disease 22 0.337
23
c LKM063 Leukemia, Chronic Myeloid 72 0.336
24
END030 End Stage Renal Failure 58 0.330
25
c LKM071 Leukemia, Chronic Lymphocytic 80 0.328
26
LYM133 Lymphoma, Hodgkin, Classic 70 0.320
27
MYL069 Myeloma, Multiple 85 0.319
28
c CHR417 Chronic Graft Versus Host Disease 57 0.315
29
DFC004 Deficiency Anemia 75 0.304
30
c PRM038 Primary Agammaglobulinemia 44 0.302
31
c CHR064 Chronic Monocytic Leukemia 34 0.300
32
ACT113 Acute Myeloblastic Leukemia with Maturation 47 0.296
33
P VSC011 Vasculitis 62 0.291
34
P BCL017 B-Cell Lymphoma 58 0.290
35
P DRR001 Diarrhea 56 0.288
36
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.285
37
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.284
38
ADL002 Adult Syndrome 70 0.279
39
MNT001 Mantle Cell Lymphoma 67 0.272
40
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 63 0.271
41
P FLL037 Follicular Lymphoma 67 0.261
42
c FLL041 Follicular Lymphoma 1 49 0.261
43
CYT008 Cytomegalovirus Infection 57 0.258
44
P CNR004 Cone-Rod Dystrophy 2 72 0.257
45
LNG099 Lung Disease 61 0.251
46
MYL031 Myeloproliferative Neoplasm 65 0.250
47
BNM001 Bone Marrow Cancer 43 0.248
48
IGG001 Iga Glomerulonephritis 48 0.247
49
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.247
50
BRK010 Burkitt Lymphoma 68 0.246
51
P SRC025 Sarcoidosis 1 71 0.238
52
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 65 0.236
53
MRG003 Marginal Zone B-Cell Lymphoma 54 0.233
54
P CHR285 Chronic Myelomonocytic Leukemia 59 0.232
55
PLS025 Plasmablastic Lymphoma 47 0.232
56
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.232
57
c HYP595 Hypertension, Essential 85 0.232
58
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.230
59
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.230
60
c SCL052 Scleroderma, Familial Progressive 63 0.228
61
INT066 Interstitial Lung Disease 60 0.226
62
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.222
63
c RHB024 Rhabdomyosarcoma 2 66 0.221
64
48X005 48,xyyy 39 0.220
65
c JVN004 Juvenile Myelomonocytic Leukemia 68 0.219
66
P PMP001 Pemphigus 55 0.219
67
c CHR684 Chronic Kidney Disease 67 0.216
68
P MYS003 Myasthenia Gravis 68 0.214
69
LYM012 Lymphoplasmacytic Lymphoma 61 0.214
70
c ACT073 Acute Leukemia 58 0.214
71
MCR004 Macroglobulinemia 50 0.214
72
P MMB011 Membranous Nephropathy 51 0.214
73
c ATM011 Autoimmune Hepatitis 62 0.208
74
MYL075 Myelodysplastic/myeloproliferative Neoplasm 50 0.205
75
P PSR002 Psoriasis 63 0.203
76
PST011 Pustulosis of Palm and Sole 53 0.203
77
MYL005 Myelofibrosis 68 0.202
78
P UVT001 Uveitis 58 0.201
79
P SYS005 Systemic Scleroderma 70 0.200
80
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 0.198
81
HDG004 Hodgkin's Granuloma 26 0.198
82
HDG006 Hodgkin's Paragranuloma 25 0.198
83
P LYM033 Lymphoproliferative Syndrome 61 0.198
84
BLL006 Bullous Pemphigoid 62 0.198
85
RFR010 Refractory Anemia 49 0.196
86
P FCL005 Focal Segmental Glomerulosclerosis 59 0.193
87
P THR014 Thrombocytopenia 68 0.190
88
MYC006 Mycosis Fungoides 66 0.185
89
SZR001 Sezary's Disease 61 0.185
90
P TCL004 T-Cell Leukemia 47 0.185
91
PMP006 Pemphigus Vulgaris, Familial 58 0.183
92
c SYS043 Systemic Lupus Erythematosus 1 43 0.182
93
CYT002 Cytokine Deficiency 44 0.181
94
PRP030 Purpura 56 0.178
95
P HPT021 Hepatitis 68 0.178
96
DRM006 Dermatitis 62 0.178
97
SPL004 Splenic Marginal Zone Lymphoma 51 0.174
98
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.174
99
P TRN020 Turner Syndrome 65 0.173
100
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.171
101
c ADL017 Adult T-Cell Leukemia 57 0.169
102
DFF005 Diffuse Large B-Cell Lymphoma 56 0.169
103
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 67 0.168
104
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.166
105
LYM051 Lymphomatoid Granulomatosis 45 0.166
106
IDP091 Idiopathic Nephrotic Syndrome 39 0.165
107
CLT003 Colitis 63 0.165
108
PRL017 Prolymphocytic Leukemia 48 0.164
109
P DRM053 Dermatitis, Atopic 67 0.163
110
P DRM010 Dermatomyositis 62 0.161
111
P LVR013 Liver Disease 68 0.160
112
RTC005 Reticulosarcoma 49 0.160
113
P DBT009 Diabetes Mellitus 65 0.159
114
ATY042 Atypical Chronic Myeloid Leukemia 49 0.157
115
SKN016 Skin Disease 63 0.156
116
P APL001 Aplastic Anemia 75 0.155
117
NTR005 Nutritional Deficiency Disease 62 0.155
118
IMM167 Immune Deficiency Disease 78 0.155
119
LPD004 Lipoid Nephrosis 48 0.154
120
c HPT001 Hepatitis C 63 0.154
121
HRY003 Hairy Cell Leukemia 55 0.153
122
MCS002 Mucositis 56 0.153
123
CNN005 Connective Tissue Disease 67 0.153
124
ANC002 Anca-Associated Vasculitis 42 0.152
125
HRP004 Herpes Zoster 60 0.150
126
P GLM044 Glomerular Disease 40 0.149
127
P CTN015 Cutaneous T Cell Lymphoma 50 0.149
128
DFF003 Diffuse Scleroderma 42 0.148
129
ANG046 Angioimmunoblastic T-Cell Lymphoma 53 0.147
130
c CHR418 Chronic Leukemia 51 0.147
131
BRN002 Bronchiolitis 59 0.145
132
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.145
133
c MCR113 Microvascular Complications of Diabetes 3 53 0.145
134
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.145
135
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.145
136
BRN012 Bronchiolitis Obliterans 56 0.142
137
ADR007 Adrenoleukodystrophy 75 0.141
138
P INF037 Inflammatory Bowel Disease 56 0.140
140
P MLT020 Multiple Sclerosis 72 0.138
141
P IGN003 Iga Nephropathy 1 50 0.138
142
CRH001 Crohn's Disease 75 0.138
143
P PRL003 Proliferative Glomerulonephritis 44 0.138
144
PRP036 Peripheral T-Cell Lymphoma 53 0.137
145
IDP011 Idiopathic Interstitial Pneumonia 64 0.136
146
P PLM036 Pulmonary Fibrosis 62 0.136
147
MCR088 Microscopic Polyangiitis 51 0.135
148
LVR012 Liver Cirrhosis 64 0.134
149
P PNM007 Pneumonia 68 0.133
150
ATM052 Autoimmune Disease 1 37 0.131
151
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 56 0.131
152
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.131
153
PST046 Post-Transplant Lymphoproliferative Disease 54 0.130
154
PLS016 Plasma Cell Leukemia 40 0.129
155
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.129
156
c MCR120 Microvascular Complications of Diabetes 7 47 0.127
157
c MCR130 Microvascular Complications of Diabetes 6 41 0.127
158
c MCR133 Microvascular Complications of Diabetes 4 41 0.127
159
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.127
160
ALL026 Allergic Hypersensitivity Disease 64 0.127
161
c ACT071 Acute Kidney Failure 60 0.127
162
GRN037 Granulomatosis with Polyangiitis 65 0.125
163
ATX019 Ataxia with Vitamin E Deficiency 48 0.125
164
FRY002 Fryns Syndrome 44 0.125
165
ATH013 Atherosclerosis Susceptibility 66 0.123
166
P HML002 Hemolytic Anemia 63 0.123
167
PYD001 Pyoderma Gangrenosum 55 0.123
168
PYD002 Pyoderma 52 0.123
169
c HPT073 Hepatitis C Virus 71 0.122
170
PLY001 Polycythemia Vera 70 0.121
171
P PLY018 Polycythemia 56 0.121
172
c PRM012 Primary Polycythemia 52 0.121
173
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.121
174
NTR003 Natural Killer Cell Leukemia 44 0.121
175
CHR286 Chronic Neutrophilic Leukemia 42 0.121
176
LRG008 Large Granular Lymphocyte Leukemia 41 0.121
177
P PLY041 Polymyositis 58 0.121
178
MMB001 Membranoproliferative Glomerulonephritis 53 0.121
179
CHC001 Chickenpox 60 0.119
180
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.119
181
P ESS003 Essential Thrombocythemia 70 0.117
182
c THR090 Thrombocythemia 1 49 0.117
183
INT054 Intraocular Lymphoma 48 0.117
184
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.117
185
P NRM001 Neuromyelitis Optica 61 0.115
186
P EXN002 Exanthem 58 0.115
187
HMN044 Human Immunodeficiency Virus Type 1 71 0.115
188
P ALP008 Alopecia 56 0.115
189
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.113
190
c FML035 Familial Hyperlipidemia 56 0.113
191
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.112
192
LPD008 Lipid Metabolism Disorder 63 0.112
193
c HPT016 Hepatitis B 60 0.112
194
P SCK005 Sickle Cell Disease 51 0.111
195
c HYP836 Hypercholesterolemia, Familial, 1 73 0.110
196
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.110
197
P KDN017 Kidney Cancer 61 0.109
198
P CRD246 Cardiovascular System Disease 56 0.109
199
CHR563 Chronic Eosinophilic Leukemia 48 0.109
200
HYP066 Hyperglycemia 61 0.108
201
P CYS018 Cystitis 60 0.108
202
P RNL015 Renal Hypertension 48 0.108
203
RNL077 Renal Fibrosis 47 0.107
204
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.107
205
SCK003 Sickle Cell Anemia 73 0.106
206
EYD002 Eye Disease 59 0.106
207
P MYS005 Myositis 56 0.106
208
ACT216 Acute Leukemia of Ambiguous Lineage 33 0.106
209
c NRM008 Neuromyelitis Optica Spectrum Disorder 32 0.106
210
P MYP004 Myopathy 65 0.104
211
P ART022 Arthritis 71 0.104
212
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 53 0.104
213
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.104
214
MCR103 Microtia 42 0.104
215
CHL079 Children's Interstitial Lung Disease 27 0.103
216
P ART021 Arteriosclerosis 55 0.101
217
P TRM003 Tremor 54 0.101
218
SPR126 Superior Semicircular Canal Dehiscence 40 0.101
219
c HMG029 Hemoglobin Se Disease 38 0.101
220
BND002 B- and T-Cell Mixed Leukemia 17 0.101
221
c ACT068 Acute Cystitis 63 0.101
222
RNL065 Renal Cell Carcinoma, Papillary, 1 74 0.099
223
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.099
224
AMN001 Amenorrhea 54 0.099
225
RTR011 Retroperitoneal Fibrosis 40 0.099
226
P RHM011 Rheumatoid Arthritis 81 0.099
227
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.099
228
P BND020 Bone Disease 60 0.099
229
PNC001 Pancytopenia 54 0.099
230
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 54 0.099
231
ISC004 Ischemia 61 0.098
232
c INT064 Intermediate Uveitis 55 0.098
233
VRL011 Viral Infectious Disease 61 0.097
234
P AMY004 Amyloidosis 71 0.096
235
P ANP001 Anaplastic Large Cell Lymphoma 61 0.096
236
P THL005 Thalassemia 60 0.096
237
c MLG054 Malignant Histiocytosis 50 0.096
238
LTH001 Lethal Midline Granuloma 44 0.096
239
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.096
240
c LCL006 Localized Scleroderma 62 0.096
241
P PNV001 Panuveitis 51 0.096
242
ULC004 Ulcerative Colitis 73 0.094
243
P PRM006 Primary Biliary Cirrhosis 62 0.094
244
P CHL066 Cholangitis 51 0.094
245
P EPD016 Epidermolysis Bullosa 54 0.094
246
P SCL015 Scleritis 48 0.094
247
c HPT003 Hepatitis a 63 0.093
248
LYM027 Lymphopenia 58 0.093
249
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 58 0.093
250
P NRB001 Neuroblastoma 72 0.093
251
CNS004 Constipation 58 0.092
252
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.091
253
c ALP101 Alpha-Thalassemia 62 0.091
254
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.091
255
PNM001 Pneumocystosis 54 0.091
256
CLF001 Cleft Lip 53 0.091
257
THR004 Thrombocytosis 51 0.091
258
c ALM001 Al Amyloidosis 51 0.091
259
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.091
260
IMM136 Immune System Disease 46 0.091
261
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.091
262
PMP004 Pemphigus Foliaceus 44 0.091
263
RDC006 Red Cell Aplasia 43 0.091
264
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.091
265
P RSP003 Respiratory Failure 75 0.091
266
OCL020 Ocular Cicatricial Pemphigoid 55 0.091
267
c MYS011 Myasthenia Gravis Congenital 29 0.091
268
HYP014 Hyperuricemia 52 0.089
269
DWN001 Down Syndrome 71 0.088
270
c ANM038 Anemia, Autoimmune Hemolytic 62 0.088
271
PPT005 Peptic Ulcer Disease 59 0.088
272
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.088
273
CYS001 Cystic Fibrosis 80 0.087
274
P VSC007 Vascular Disease 64 0.087
275
KPS004 Kaposi Sarcoma 76 0.086
276
HMG005 Hemoglobinopathy 56 0.086
277
c PST005 Posterior Uveitis 54 0.086
278
P CTN003 Cutaneous Lupus Erythematosus 53 0.086
279
P HML001 Hemolytic-Uremic Syndrome 53 0.086
280
c INF145 Infantile Liver Failure Syndrome 1 50 0.086
281
CLS052 Classic Hairy Cell Leukemia 27 0.086
282
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.085
283
CLF004 Cleft Lip/palate 55 0.083
284
P MST002 Mast-Cell Leukemia 48 0.083
285
P PRR002 Pure Red-Cell Aplasia 48 0.083
286
P SCL009 Sclerosing Cholangitis 47 0.083
287
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.083
288
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.083
289
P ESP024 Esophagitis 62 0.083
290
P ENC004 Encephalitis 62 0.083
291
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.083
292
ERY051 Erythroleukemia, Familial 57 0.083
293
BCT022 Bacterial Infectious Disease 56 0.083
294
LYM005 Lymphocele 35 0.083
295
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.080
296
ALS001 Alstrom Syndrome 63 0.080
297
P PNC044 Pancreatitis 61 0.080
298
CHR001 Churg-Strauss Syndrome 61 0.080
299
ACQ007 Acquired Immunodeficiency Syndrome 60 0.080
300
P MYC008 Myocarditis 60 0.080
301
PLS011 Plasmacytoma 57 0.080
302
P LCH002 Lichen Planus 55 0.080
303
c ACT134 Acute Liver Failure 51 0.080
304
c NPH049 Nephrotic Syndrome, Type 2 48 0.080
305
c FCL025 Focal Segmental Glomerulosclerosis 1 47 0.080
306
CNG028 Congenital Hypoplastic Anemia 46 0.080
307
RFR002 Refractory Hairy Cell Leukemia 32 0.080
308
SVR004 Severe Combined Immunodeficiency 74 0.079
309
P HYP098 Hypereosinophilic Syndrome 66 0.079
310
THR024 Thrombosis 57 0.079
311
c BKV001 Bk-Virus Nephropathy 23 0.079
312
SCH036 Scheie Syndrome 72 0.078
313
P SKN015 Skin Carcinoma 67 0.078
314
HYP056 Hypoglycemia 66 0.077
315
P URT039 Urticaria 58 0.077
316
CLB010 Coloboma of Macula 53 0.077
317
INT067 Interstitial Nephritis 47 0.077
318
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 46 0.077
319
FBR089 Fibrosclerosis, Multifocal 38 0.077
320
P BDY004 Body Mass Index Quantitative Trait Locus 11 77 0.076
321
P HYP750 Hypertriglyceridemia, Familial 62 0.076
322
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.076
323
c BDY021 Body Mass Index Quantitative Trait Locus 20 53 0.076
324
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.076
325
c PSR017 Psoriasis 2 50 0.076
326
c PSR023 Psoriasis 1 49 0.076
327
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.076
328
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.076
329
c BDY010 Body Mass Index Quantitative Trait Locus 4 47 0.076
330
c BDY015 Body Mass Index Quantitative Trait Locus 12 47 0.076
331
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.076
332
c BDY011 Body Mass Index Quantitative Trait Locus 10 46 0.076
333
ACT003 Acute Kidney Tubular Necrosis 45 0.076
334
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.076
335
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.076
336
c PSR028 Psoriasis 7 39 0.076
337
c PSR032 Psoriasis 11 39 0.076
338
c PSR018 Psoriasis 13 39 0.076
339
CCT002 Cicatricial Pemphigoid 50 0.075
340
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.075
341
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.073
342
c FNC027 Fanconi Anemia, Complementation Group a 82 0.073
343
P HRT032 Heart Disease 76 0.073
344
c BTT014 Beta-Thalassemia 73 0.073
345
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 66 0.073
346
MGK001 Megakaryocytic Leukemia 64 0.073
347
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.073
348
c LKM070 Leukemia, Acute Monocytic 54 0.073
349
CYS036 Cystinosis, Nephropathic 52 0.073
350
ENT011 Enterocolitis 51 0.073
351
P FNC004 Fanconi Syndrome 50 0.073
352
HMG002 Hemoglobinuria 49 0.073
353
EPD006 Epidermolysis Bullosa Acquisita 49 0.073
355
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.073
356
PLY043 Polyomavirus Allograft Nephropathy 13 0.073
357
CRB039 Cerebrovascular Disease 69 0.073
358
NRM005 Neuromuscular Disease 64 0.073
359
CHL068 Cholestasis 61 0.073
360
IRN002 Iron Metabolism Disease 58 0.073
361
P GST044 Gastritis 56 0.073
362
P MCR115 Microvascular Complications of Diabetes 5 67 0.070
363
c CHL119 Cholangitis, Primary Sclerosing 58 0.070
364
ERY003 Erythema Multiforme 58 0.070
365
P ANT006 Antiphospholipid Syndrome 55 0.070
366
P CNT005 Central Nervous System Lymphoma 54 0.070
367
47X002 47,xyy 49 0.070
368
PNN001 Panniculitis 49 0.070
369
URT010 Ureteral Obstruction 46 0.070
370
c INH020 Inherited Metabolic Disorder 46 0.070
371
PLS003 Plasmacytic Leukemia 26 0.070
372
P MNN013 Meningitis 66 0.070
373
P BLD124 Bleeding Disorder, Platelet-Type, 11 62 0.070
374
P CTR002 Cataract 61 0.070
375
P SZR006 Seizure Disorder 59 0.070
376
VSL002 Visual Epilepsy 57 0.070
377
P NRP001 Neuropathy 57 0.070
378
P PLY019 Polyneuropathy 56 0.070
379
ACT058 Active Peptic Ulcer Disease 55 0.070
380
P RPD001 Rapidly Progressive Glomerulonephritis 45 0.070
381
P PNC035 Pancreatic Cancer 85 0.066
382
P NRF023 Neurofibromatosis, Type Ii 77 0.066
383
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.066
384
SRC014 Sarcoma 66 0.066
385
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.066
386
P CRN018 Coronary Artery Anomaly 64 0.066
387
P CRN300 Coronary Heart Disease 1 64 0.066
388
TKY002 Takayasu Arteritis 62 0.066
389
P BRN022 Bronchiectasis 60 0.066
390
c ACT027 Acute Pancreatitis 60 0.066
391
P PLY017 Polyarteritis Nodosa 59 0.066
392
EXT034 Extrinsic Allergic Alveolitis 58 0.066
393
P INF032 Infertility 58 0.066
394
BLR008 Bilirubin Metabolic Disorder 58 0.066
395
HNC001 Henoch-Schoenlein Purpura 54 0.066
396
P HST010 Histiocytosis 53 0.066
397
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.066
398
ACR041 Acromelic Frontonasal Dysostosis 53 0.066
399
DMY004 Demyelinating Disease 52 0.066
400
SPN035 Spindle Cell Sarcoma 51 0.066
401
HYP081 Hypolipoproteinemia 51 0.066
402
CMB081 Combined Immunodeficiency, X-Linked 47 0.066
403
P PLY020 Polyradiculoneuropathy 47 0.066
404
CRS001 Crescentic Glomerulonephritis 44 0.066
405
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 40 0.066
406
THR123 Thrombotic Microangiopathy 39 0.066
407
ALL012 Allergic Angiitis 24 0.066
409
STR067 Stroke, Ischemic 80 0.065
410
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.065
411
c MCR129 Microvascular Complications of Diabetes 1 66 0.063
412
CLF027 Cleft Palate, Isolated 65 0.063
413
ACT119 Acute Promyelocytic Leukemia 63 0.063
414
P INT143 Interstitial Cystitis 62 0.063
415
ADL030 Adult-Onset Still's Disease 58 0.063
416
P PYL005 Pyelonephritis 57 0.063
417
MCL006 Macular Retinal Edema 56 0.063
418
HYP748 Hypertelorism 50 0.063
419
c PRM226 Primary Central Nervous System Lymphoma 47 0.063
420
EVN001 Evans' Syndrome 47 0.063
421
c MCR112 Microvascular Complications of Diabetes 2 41 0.063
422
C3G002 C3 Glomerulopathy 39 0.063
423
NDL003 Nodular Nonsuppurative Panniculitis 39 0.063
424
NRS005 Neurosarcoidosis 36 0.063
425
c PRM039 Primary Angiitis of the Central Nervous System 34 0.063
426
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 18 0.063
427
P BRS047 Breast Cancer 97 0.062
428
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.062
429
CLN015 Colon Adenocarcinoma 64 0.062
430
SQM006 Squamous Cell Carcinoma 60 0.062
431
P OPT006 Optic Nerve Disease 58 0.062
432
ESP020 Esophageal Atresia 56 0.062
433
RHM027 Rheumatic Disease 56 0.062
434
DYS073 Dysphagia 51 0.062
435
ACT029 Acute Interstitial Pneumonia 45 0.062
436
HMR023 Hemorrhagic Cystitis 39 0.062
437
SYS071 Systemic Autoimmune Disease 37 0.062
438
P HPT023 Hepatocellular Carcinoma 100 0.060
439
P PRS040 Prostate Cancer 98 0.058
440
P WSK001 Wiskott-Aldrich Syndrome 72 0.058
441
P DMN001 Diamond-Blackfan Anemia 69 0.058
442
MLN008 Melanoma 69 0.058
443
P INF038 Influenza 68 0.058
444
P CHR012 Chronic Granulomatous Disease 68 0.058
445
SKN019 Skin Melanoma 68 0.058
446
P DYS007 Dyskeratosis Congenita 67 0.058
447
PRT036 Peritonitis 65 0.058
448
INC002 Inclusion Body Myositis 65 0.058
449
DGR001 Digeorge Syndrome 64 0.058
450
P THR005 Thrombotic Thrombocytopenic Purpura 62 0.058
451
PRT013 Portal Hypertension 61 0.058
452
LNG108 Langerhans Cell Histiocytosis 59 0.058
453
P HDC001 Headache 58 0.058
454
HPT046 Hepatic Veno-Occlusive Disease 57 0.058
455
ACT200 Acute Monoblastic Leukemia 55 0.058
456
PPL022 Papilloma 55 0.058
457
VLC001 Velocardiofacial Syndrome 55 0.058
458
P MNC007 Monocytic Leukemia 54 0.058
459
HYP063 Hypersplenism 53 0.058
460
GNG012 Gingival Overgrowth 51 0.058
461
P HYP077 Hypertrichosis 51 0.058
462
c OPT050 Opitz Gbbb Syndrome, Type Ii 49 0.058
463
ENT004 Enthesopathy 49 0.058
464
ACT098 Acute Erythroid Leukemia 48 0.058
465
MLT075 Multifocal Motor Neuropathy 47 0.058
466
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.058
467
IDP033 Idiopathic Edema 43 0.058
468
SQM002 Squamous Cell Papilloma 43 0.058
469
P DMY001 Demyelinating Polyneuropathy 41 0.058
470
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.058
471
c CHR682 Chronic Bilirubin Encephalopathy 39 0.058
472
CHR463 Chronic Actinic Dermatitis 37 0.058
473
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.058
474
HRP008 Herpes Simiae 25 0.058
475
c ADL093 Adult Acute Monocytic Leukemia 20 0.058
476
MSC007 Muscle Hypertrophy 64 0.057
477
c FNC043 Fanconi Anemia, Complementation Group E 63 0.057
478
P SJG008 Sjogren Syndrome 57 0.057
479
KRT006 Keratoconjunctivitis 54 0.057
480
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.057
481
KRT001 Keratoconjunctivitis Sicca 50 0.057
482
URM002 Uremia 49 0.057
484
c THR092 Thrombophilia Due to Thrombin Defect 73 0.054
485
P MTC003 Metachromatic Leukodystrophy 71 0.054
486
P KRB001 Krabbe Disease 70 0.054
487
P NRV007 Nervous System Disease 66 0.054
488
PSR001 Psoriatic Arthritis 62 0.054
489
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.054
490
CHL028 Childhood Type Dermatomyositis 60 0.054
491
P LKD001 Leukodystrophy 60 0.054
492
c CHL140 Chilblain Lupus 1 57 0.054
493
c CNT035 Central Nervous System Disease 54 0.054
494
c HYP768 Hyperlipoproteinemia, Type I 53 0.054
495
FML026 Familial Lipoprotein Lipase Deficiency 52 0.054
496
MYL001 Myelitis 51 0.054
497
STM007 Stomatitis 51 0.054
498
P PLG001 Pelger-Huet Anomaly 50 0.054
499
PRX001 Peroxisomal Disease 46 0.054
500
ISC015 Ischemic Colitis 45 0.054
501
ANT039 Antisynthetase Syndrome 44 0.054
502
MNT303 Mental Retardation, X-Linked, Syndromic, Cabezas Type 41 0.054
503
FRN020 Frontal Fibrosing Alopecia 40 0.054
504
ADR022 Adrenomyeloneuropathy 39 0.054
505
RFR004 Refractory Hematologic Cancer 30 0.054
506
P OVR096 Overlap Myositis 28 0.054
507
SYN092 Syndromic X-Linked Intellectual Disability Cabezas Type 24 0.054
508
GLS018 Glass Syndrome 53 0.053
509
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.053
510
P OST002 Osteoporosis 74 0.053
511
P HRP006 Herpes Simplex 65 0.053
512
P ENC018 Encephalopathy 61 0.053
513
P ALP009 Alopecia Areata 60 0.053
514
P PLY014 Polycystic Kidney Disease 60 0.053
515
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 59 0.053
516
HYP005 Hypokalemia 56 0.053
517
GST037 Gastroparesis 54 0.053
518
c ACT020 Acute T Cell Leukemia 54 0.053
519
CRH005 Crohn's Colitis 53 0.053
520
MYL020 Myelomeningocele 51 0.053
521
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.053
522
DDN006 Duodenitis 48 0.053
523
c ATM099 Autoimmune Uveitis 44 0.053
524
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.053
525
ALL014 Allergic Encephalomyelitis 40 0.053
526
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 39 0.053
527
P PLY188 Polyendocrinopathy 33 0.053
528
c PRM339 Primary Glomerular Disease 31 0.053
530
CRV035 Cervical Cancer 76 0.049
531
MRF001 Marfan Syndrome 76 0.049
532
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 0.049
533
P MYC084 Mycobacterium Tuberculosis 1 69 0.049
534
P CRN037 Craniosynostosis 68 0.049
535
FCT007 Factor Vii Deficiency 67 0.049
536
P ASP006 Aspergillosis 67 0.049
537
P AGM001 Agammaglobulinemia 66 0.049
538
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.049
539
PRT037 Pertussis 66 0.049
540
P THY023 Thymoma 65 0.049
541
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.049
542
P RHB003 Rhabdomyosarcoma 63 0.049
543
ALC006 Alcoholic Hepatitis 62 0.049
544
P TST021 Testicular Germ Cell Tumor 61 0.049
545
OST003 Osteonecrosis 61 0.049
546
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.049
547
HYD002 Hydronephrosis 60 0.049
548
URN010 Urinary Tract Obstruction 58 0.049
549
HRL003 Hurler Syndrome 58 0.049
550
P URF003 Urofacial Syndrome 1 57 0.049
551
PGM001 Pigmented Villonodular Synovitis 57 0.049
552
DYS164 Dyskeratosis Congenita, X-Linked 56 0.049
553
VGN017 Vaginal Cancer 56 0.049
554
MRD002 Marden-Walker Syndrome 55 0.049
555
VGT001 Vogt-Koyanagi-Harada Disease 55 0.049
556
PRN038 Prune Belly Syndrome 54 0.049
557
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 0.049
558
ART140 Arteries, Anomalies of 53 0.049
559
c DMN023 Diamond-Blackfan Anemia 1 53 0.049
560
c THY107 Thymoma, Familial 53 0.049
561
CRT016 Carotid Artery Disease 52 0.049
562
c PST041 Posterior Urethral Valves 51 0.049
563
SPP010 Suppressor of Tumorigenicity 3 51 0.049
564
IRD001 Iridocyclitis 51 0.049
565
BRN014 Bronchopneumonia 51 0.049
566
URN009 Urinary System Disease 49 0.049
567
ATS010 Autosomal Recessive Disease 49 0.049
568
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.049
569
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 48 0.049
570
ADN001 Adenosine Deaminase Deficiency 47 0.049
571
RTN023 Retinitis 47 0.049
572
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 46 0.049
573
KRT008 Keratopathy 46 0.049
574
GST010 Gestational Trophoblastic Neoplasm 46 0.049
575
EXT010 Extramedullary Plasmacytoma 46 0.049
576
c ACQ014 Acquired Hemophilia 45 0.049
577
GRN017 Granulocytopenia 45 0.049
578
P TST026 Testicular Germ Cell Cancer 44 0.049
579
c HYP272 Hypercholesterolemia, Familial, 3 44 0.049
580
NRR001 Neuroretinitis 43 0.049
581
49X002 49,xxxxy Syndrome 42 0.049
582
LNR006 Linear Iga Disease 40 0.049
583
P BCL005 B Cell Prolymphocytic Leukemia 39 0.049
584
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.049
585
TRP005 Trophoblastic Neoplasm 38 0.049
586
OVR094 Ovarian Epithelial Cancer 38 0.049
587
GND003 Gonadal Disease 38 0.049
588
LTT002 Letterer-Siwe Disease 34 0.049
589
GRM010 Germ Cells Tumors 34 0.049
590
c ATM045 Autoimmune Glomerulonephritis 33 0.049
591
GNT019 Giant Cell Myocarditis 30 0.049
592
c TST046 Testicular Germ Cell Tumor 1 29 0.049
593
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 28 0.049
594
MLG164 Malignant Epithelial Tumor of Ovary 26 0.049
596
PLY179 Polyomavirus-Associated Nephropathy 24 0.049
597
P MYC007 Myocardial Infarction 71 0.047
598
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.047
599
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.047
600
PLM012 Pulmonary Sarcoidosis 54 0.047
601
c SPN225 Spondyloarthropathy 1 74 0.044
602
P FML011 Familial Adenomatous Polyposis 72 0.044
603
P TYS001 Tay-Sachs Disease 69 0.044
604
BRN024 Bronchitis 69 0.044
605
P CLC063 Celiac Disease 1 68 0.044
606
SND001 Sandhoff Disease 68 0.044
607
PNC129 Pancreatic Adenocarcinoma 68 0.044
608
c JVN010 Juvenile Rheumatoid Arthritis 67 0.044
609
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.044
610
SVR097 Severe Cutaneous Adverse Reaction 67 0.044
611
c MCP001 Mucopolysaccharidosis Iii 66 0.044
612
c DPH024 Diaphragmatic Hernia, Congenital 65 0.044
613
LYS012 Lysosomal Acid Lipase Deficiency 64 0.044
614
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.044
615
c PRC016 Pre-Eclampsia 64 0.044
616
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.044
617
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.044
618
c GM1007 Gm1 Gangliosidosis 62 0.044
619
P TXP001 Toxoplasmosis 61 0.044
620
MCR013 Microphthalmia 61 0.044
621
STT001 Status Epilepticus 60 0.044
622
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.044
623
PLM033 Pulmonary Embolism 59 0.044
624
CMR002 Coumarin Resistance 56 0.044
625
GDP001 Goodpasture Syndrome 55 0.044
626
CLR030 Clear Cell Renal Cell Carcinoma 54 0.044
627
c ATM024 Autoimmune Pancreatitis 54 0.044
628
SPN051 Spondylitis 52 0.044
629
P HMP007 Hemophilia 52 0.044
630
OCL069 Ocular Motor Apraxia 52 0.044
631
MCR141 Mucormycosis 51 0.044
632
PLR008 Pleurisy 51 0.044
633
CRT013 Carotid Stenosis 50 0.044
634
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.044
635
MNN009 Meningoencephalitis 49 0.044
636
CRY004 Cryoglobulinemia 49 0.044
637
SPL018 Splenomegaly 48 0.044
638
P MCL001 Mucolipidosis 47 0.044
639
CLL014 Cll/sll 45 0.044
640
P GNG009 Gangliosidosis 44 0.044
641
OBS082 Obstructive Nephropathy 44 0.044
642
MGS001 Megaesophagus 44 0.044
643
PRN049 Paraneoplastic Pemphigus 43 0.044
644
DSC009 Discoid Lupus Erythematosus 43 0.044
645
CNT046 Central Nervous System Vasculitis 43 0.044
646
RDN001 Reading Disorder 41 0.044
647
CRN020 Coronary Restenosis 40 0.044
648
ERM002 Ear Malformation 39 0.044
649
CRB001 Cerebral Lymphoma 39 0.044
650
CFH006 Cfhr5 Deficiency 36 0.044
651
INC022 Inclusion-Cell Disease 34 0.044
652
LYM043 Lymphocytic Hypophysitis 33 0.044
653
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.044
654
INF009 Inflammatory Spondylopathy 32 0.044
655
CRN051 Craniofacial Microsomia 29 0.044
656
ERY066 Erythema Multiforme Major 28 0.044
657
IGP001 Iga Pemphigus 26 0.044
658
NRL016 Neural Tube Defects 83 0.043
659
c INF071 Inflammatory Bowel Disease 1 68 0.043
660
P HYP069 Hyperparathyroidism 63 0.043
661
GST050 Gastrointestinal System Disease 56 0.043
662
TXC002 Toxic Encephalopathy 52 0.043
663
PTT041 Pituitary Stalk Interruption Syndrome 51 0.043
664
CRD043 Ceroid Storage Disease 44 0.043
665
NRN005 Neuronal Ceroid-Lipofuscinoses 42 0.043
666
c ACT004 Acute Diarrhea 40 0.043
667
CDQ001 Cauda Equina Syndrome 39 0.043
668
RFR013 Refractory Celiac Disease 35 0.043
669
PLY021 Polyradiculopathy 34 0.043
670
SPT004 Septic Arthritis 58 0.038
671
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.038
672
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.038
673
c DLT002 Dilated Cardiomyopathy 80 0.038
674
PRP027 Peripheral Vascular Disease 72 0.038
675
c MCP050 Mucopolysaccharidosis, Type Ii 71 0.038
676
P HYP802 Hypocalcemia, Autosomal Dominant 1 70 0.038
677
P PLM037 Pulmonary Hypertension 69 0.038
678
MST024 Mastocytosis, Cutaneous 68 0.038
679
c MCP052 Mucopolysaccharidosis, Type Vi 68 0.038
680
CHD001 Chediak-Higashi Syndrome 66 0.038
681
P SHW006 Shwachman-Diamond Syndrome 1 66 0.038
682
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.038
683
GST092 Gastroesophageal Reflux 65 0.038
684
c MNN047 Mannosidosis, Alpha B, Lysosomal 65 0.038
685
P MTR014 Motor Neuron Disease 65 0.038
686
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.038
687
GT001 Gout 64 0.038
688
P MST009 Mastocytosis 64 0.038
689
c MCP049 Mucopolysaccharidosis, Type Vii 64 0.038
690
FCS002 Fucosidosis 63 0.038
691
TXC005 Toxic Shock Syndrome 62 0.038
692
INT002 Intermittent Claudication 62 0.038
693
MSL001 Measles 61 0.038
694
ASP002 Aspartylglucosaminuria 60 0.038
695
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.038
696
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.038
697
PRT058 Pure Autonomic Failure 60 0.038
698
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.038
699
CNT047 Contact Dermatitis 58 0.038
700
P MMP001 Mumps 58 0.038
701
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.038
702
PLY023 Polycystic Liver Disease 58 0.038
703
P PRP019 Peripheral Nervous System Disease 58 0.038
704
SFT003 Soft Tissue Sarcoma 57 0.038
705
AVN001 Avian Influenza 56 0.038
706
SKN022 Skin Squamous Cell Carcinoma 56 0.038
707
P HYP024 Hypoparathyroidism 56 0.038
708
ALL010 Allergic Contact Dermatitis 56 0.038
709
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 56 0.038
710
P LTR001 Lateral Sclerosis 54 0.038
711
GLC003 Glucose Intolerance 54 0.038
712
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 54 0.038
713
PRC013 Pericarditis 54 0.038
714
P THY032 Thyroiditis 53 0.038
715
EXP004 Exophthalmos 53 0.038
716
GLM004 Gliomatosis Cerebri 53 0.038
717
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.038
718
c HPT007 Hepatitis E 53 0.038
719
RVS001 Revesz Syndrome 53 0.038
720
LYS002 Lysosomal Storage Disease 52 0.038
721
c VRL010 Viral Hepatitis 52 0.038
722
ILS001 Ileus 51 0.038
723
HPT014 Hepatorenal Syndrome 51 0.038
724
P OVR082 Overgrowth Syndrome 50 0.038
725
MTB004 Metabolic Acidosis 50 0.038
726
CYT005 Cytomegalovirus Retinitis 49 0.038
727
CGN006 Cogan Syndrome 49 0.038
728
MYL003 Myeloid Sarcoma 49 0.038
729
BRD025 Birdshot Chorioretinopathy 49 0.038
730
NRL018 Neural Tube Defects, Folate-Sensitive 49 0.038
731
BBS001 Babesiosis 49 0.038
732
SPH010 Sphingolipidosis 48 0.038
733
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 48 0.038
734
RYN005 Raynaud Phenomenon 47 0.038
735
HYR002 Hoyeraal Hreidarsson Syndrome 47 0.038
736
ANR004 Anuria 46 0.038
737
TCL003 T Cell Deficiency 45 0.038
738
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.038
739
HRL004 Hurler-Scheie Syndrome 44 0.038
740
KMR001 Kimura Disease 44 0.038
741
TRP009 Triple X Syndrome 43 0.038
742
c MYL058 Myeloproliferative Syndrome, Transient 43 0.038
743
P PRT026 Parotitis 42 0.038
744
BCK006 Back Pain 42 0.038
745
ACT088 Acute Insulin Response 41 0.038
746
THR035 Thrombasthenia 41 0.038
747
LKP003 Leukoplakia 40 0.038
748
ORL012 Oral Leukoplakia 39 0.038
749
ENT001 Enterocele 39 0.038
750
c MLG074 Malignant Mesenchymoma 39 0.038
751
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 39 0.038
752
MST004 Mast Cell Neoplasm 39 0.038
753
EXT007 Extracutaneous Mastocytoma 38 0.038
754
MCP033 Mucopolysaccharidoses 38 0.038
755
TTH004 Tethered Spinal Cord Syndrome 36 0.038
756
HDG005 Hodgkin's Lymphoma, Mixed Cellularity 35 0.038
757
ATY022 Atypical Coarctation of Aorta 34 0.038
758
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.038
759
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.038
760
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 34 0.038
761
CYT018 Cytochrome P450 2d6 Variant 27 0.038
762
c SYS066 Systemic Polyarteritis Nodosa 27 0.038
763
PGM030 Pigmentation Anomaly of the Skin 25 0.038
764
P PLM069 Pulmonary Venous Return Anomaly 25 0.038
765
HMP028 Hemophagocytic Syndrome Associated with an Infection 24 0.038
766
CHR208 Chromosome 17p Deletion 23 0.038
767
BLL015 Bullous Lichen Planus 21 0.038
768
PFF001 Pfeiffer Syndrome 80 0.031
769
INS024 Insulin-Like Growth Factor I 80 0.031
770
CNN003 Conn's Syndrome 79 0.031
771
P LNG064 Lung Cancer Susceptibility 3 78 0.031
772
c ATR087 Atrial Standstill 1 74 0.031
773
MSC157 Muscular Dystrophy, Duchenne Type 72 0.031
774
WLS001 Wilson Disease 71 0.031
775
GST040 Gastric Adenocarcinoma 71 0.031
776
CNG034 Congestive Heart Failure 70 0.031
777
P TTR001 Tetralogy of Fallot 70 0.031
778
c MGR028 Migraine with or Without Aura 1 70 0.031
779
P ALP004 Alport Syndrome 69 0.031
780
KRT019 Keratitis, Hereditary 68 0.031
781
P LPR021 Leprosy 3 67 0.031
782
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.031
783
P MSC005 Muscular Dystrophy 66 0.031
784
CHR103 Charge Syndrome 66 0.031
785
LNG039 Lung Squamous Cell Carcinoma 66 0.031
786
c HMP029 Hemophilia a 65 0.031
787
BRR014 Barrett Esophagus 65 0.031
788
P EPD009 Epidermolysis Bullosa Dystrophica 65 0.031
789
DPR016 Depression 64 0.031
790
P PRM002 Primary Hyperoxaluria 63 0.031
791
ANR007 Anorexia Nervosa 63 0.031
792
P ANR048 Aniridia 1 63 0.031
793
P ART023 Arthropathy 63 0.031
794
c WLM018 Wilms Tumor 5 62 0.031
795
TRN015 Transient Cerebral Ischemia 62 0.031
796
MDD011 Mood Disorder 62 0.031
797
HYD038 Hydrops Fetalis, Nonimmune 62 0.031
798
P CRG003 Crigler-Najjar Syndrome, Type I 62 0.031
799
CRC021 Carcinosarcoma 62 0.031
800
SPN186 Spinal Cord Injury 61 0.031
801
SDD001 Sudden Infant Death Syndrome 61 0.031
802
ACN002 Acanthosis Nigricans 61 0.031
803
CRD223 Cardiac Arrhythmia 61 0.031
804
FBR086 Fibrolamellar Carcinoma 60 0.031
805
P GLL022 Guillain-Barre Syndrome 60 0.031
806
ECT006 Ectodermal Dysplasia 60 0.031
807
MXD005 Mixed Connective Tissue Disease 60 0.031
808
P TRC086 Trichohepatoenteric Syndrome 1 59 0.031
809
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.031
810
P INT070 Intestinal Obstruction 59 0.031
811
BRS051 Breast Disease 58 0.031
812
c DWL002 Dowling-Degos Disease 1 58 0.031
813
P CND004 Candidiasis 58 0.031
814
PYR041 Pyruvate Kinase Deficiency of Red Cells 58 0.031
815
CPR004 Coproporphyria, Hereditary 58 0.031
816
DSS009 Disseminated Intravascular Coagulation 58 0.031
817
PLG002 Plague 57 0.031
818
MNT002 Mental Depression 57 0.031
819
TRN018 Transitional Cell Carcinoma 57 0.031
820
INT303 Intracranial Hypertension, Idiopathic 57 0.031
821
DBL002 Double Outlet Right Ventricle 56 0.031
822
HMF006 Hemifacial Microsomia 56 0.031
823
c BCT007 Bacterial Meningitis 56 0.031
824
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 56 0.031
825
FCT001 Factor Viii Deficiency 55 0.031
826
P DBT005 Diabetes Insipidus 55 0.031
827
PLM010 Pulmonary Edema 55 0.031
828
HMP005 Hemiplegia 55 0.031
829
FRY006 Fryns Microphthalmia Syndrome 55 0.031
830
P MCR010 Microcephaly 55 0.031
831
RLP001 Relapsing Polychondritis 54 0.031
832
LST001 Listeriosis 54 0.031
833
PTT009 Pituitary Gland Disease 54 0.031
834
PLM070 Pulmonic Stenosis 54 0.031
835
P RTN016 Retinal Degeneration 54 0.031
836
LYM004 Lymphoid Interstitial Pneumonia 53 0.031
837
MST005 Mastitis 53 0.031
838
P LYM025 Lymphedema 53 0.031
839
INT051 Intussusception 53 0.031
840
GST023 Gastric Ulcer 53 0.031
841
THR013 Thoracic Outlet Syndrome 53 0.031
842
P PLM006 Pulmonary Alveolar Proteinosis 53 0.031
843
P SHR001 Short Bowel Syndrome 53 0.031
844
STF002 Stiff Skin Syndrome 52 0.031
845
ERD001 Erdheim-Chester Disease 52 0.031
846
CHR073 Choreatic Disease 52 0.031
847
STR008 Strongyloidiasis 51 0.031
848
HYP074 Hypersensitivity Vasculitis 51 0.031
849
P ECL001 Eclampsia 51 0.031
850
c PYR010 Peyronie's Disease 51 0.031
851
P PRC012 Pericardial Effusion 51 0.031
852
P TMP001 Temporal Lobe Epilepsy 51 0.031
853
c PRM108 Primary Progressive Multiple Sclerosis 51 0.031
854
CHR078 Chorioretinitis 51 0.031
855
PRT018 Portal Vein Thrombosis 50 0.031
856
P DDN001 Duodenal Ulcer 50 0.031
857
ILT001 Ileitis 50 0.031
858
FSC004 Fasciitis 50 0.031
859
BLR001 Biliary Atresia 50 0.031
860
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 50 0.031
861
FDL002 Food Allergy 50 0.031
862
NPH010 Nephrosclerosis 50 0.031
863
c PSR021 Psoriasis 14, Pustular 50 0.031
864
RNL011 Renal Osteodystrophy 50 0.031
865
BLL003 Bell's Palsy 49 0.031
866
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 49 0.031
867
HPT009 Hepatopulmonary Syndrome 49 0.031
868
NCR007 Necrotizing Fasciitis 49 0.031
869
BNR002 Bone Resorption Disease 49 0.031
870
PPL021 Papilledema 49 0.031
871
CRP032 Corpus Callosum, Agenesis of 49 0.031
872
MCR020 Microsporidiosis 49 0.031
873
WTH001 Withdrawal Disorder 49 0.031
874
SCT005 Scott Syndrome 49 0.031
875
ASP007 Aspiration Pneumonia 48 0.031
876
CRY014 Cryptococcal Meningitis 48 0.031
877
NCR004 Nocardiosis 48 0.031
878
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.031
879
DRY001 Dry Eye Syndrome 48 0.031
880
c BCT013 Bacterial Pneumonia 47 0.031
881
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.031
882
MDS022 Mediastinitis 47 0.031
883
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.031
884
PDT035 Pediatric Systemic Lupus Erythematosus 47 0.031
885
HMP001 Hemopericardium 47 0.031
886
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.031
887
RTN001 Retinal Vasculitis 47 0.031
888
c ACT076 Acute Myocarditis 47 0.031
889
P MYC033 Myoclonus 46 0.031
890
FLL008 Folliculitis 46 0.031
891
P TRN034 Transverse Myelitis 46 0.031
892
ACT055 Actinomycosis 46 0.031
893
HYP059 Hypertelorism, Microtia, Facial Clefting Syndrome 45 0.031
894
HYP034 Hypertensive Encephalopathy 45 0.031
895
CHR008 Choroiditis 45 0.031
896
CRB004 Cerebral Artery Occlusion 45 0.031
897
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.031
898
ORL013 Oral Lichen Planus 45 0.031
899
c ACT042 Acute Pyelonephritis 45 0.031
900
DVR002 Diverticulitis 44 0.031
901
SBC012 Subcorneal Pustular Dermatosis 44 0.031
902
CRD003 Cardiac Sarcoidosis 44 0.031
903
HPT004 Hepatic Coma 44 0.031
904
DRG024 Drug Allergy 44 0.031
905
DYS018 Dysostosis 43 0.031
906
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.031
907
P CLS010 Cluster Headache 43 0.031
908
P HYP087 Hypotrichosis 42 0.031
909
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.031
910
ERY017 Erythema Elevatum Diutinum 42 0.031
911
CLF056 Cleft Lip with or Without Cleft Palate 42 0.031
912
LMB024 Limbic Encephalitis 41 0.031
913
c FML015 Familial Nephrotic Syndrome 41 0.031
914
ULC007 Ulcerative Stomatitis 39 0.031
915
ORF044 Orofacial Granulomatosis 38 0.031
916
NCR002 Necrobiosis Lipoidica 38 0.031
917
P PST059 Pustular Psoriasis 38 0.031
918
TRC005 Tracheal Stenosis 38 0.031
919
c ATM075 Autoimmune Encephalitis 38 0.031
920
c ACQ042 Acquired Hemophilia a 37 0.031
921
ATX010 Ataxia Neuropathy Spectrum 37 0.031
922
LYM010 Lymph Node Tuberculosis 37 0.031
923
P ATM020 Autoimmune Enteropathy 35 0.031
924
c ATM022 Autoimmune Myocarditis 35 0.031
925
HNS001 Hansen's Disease 35 0.031
926
KDN013 Kidney Hypertrophy 35 0.031
927
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.031
928
RHM036 Rheumatoid Arthritis Interstitial Lung Disease 33 0.031
929
NNT011 Neonatal Anemia 33 0.031
930
CLN006 Colonic Pseudo-Obstruction 33 0.031
931
MLT035 Multifocal Choroiditis 32 0.031
932
ORL022 Oral Erosive Lichen 32 0.031
933
ACT064 Acute Necrotizing Encephalitis 32 0.031
934
ACR017 Acrofacial Dysostosis 31 0.031
935
PNC059 Punctate Inner Choroidopathy 31 0.031
936
c PST008 Posterior Scleritis 30 0.031
937
c ANT023 Anterior Scleritis 30 0.031
938
MYC088 Mycobacterium Avium Complex Infections 30 0.031
939
GRN033 Granulomatous Mastitis 29 0.031
940
TBL025 Tubulointerstitial Nephritis with Uveitis 29 0.031
941
LST003 Listeria Meningitis 28 0.031
942
RRD056 Rare Disease in Surgical Orthopedic 28 0.031
943
CTN019 Cutaneous Polyarteritis Nodosa 28 0.031
944
ACT162 Acute Sensory Ataxic Neuropathy 27 0.031
945
MDD015 Mid-Dermal Elastolysis 27 0.031
946
DFF031 Diffuse Alveolar Hemorrhage 26 0.031
947
FBR028 Fibrosing Mediastinitis 26 0.031
948
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 26 0.031
949
MCR039 Macrophagic Myofasciitis 25 0.031
950
MCR093 Microtia-Anotia 25 0.031
951
UND004 Undetermined Colitis 24 0.031
952
c NPH105 Nephrotic Syndrome, Type 17 24 0.031
953
SVR055 Severe Immune-Mediated Enteropathy 24 0.031
954
FDL001 Fiedler's Myocarditis 23 0.031
955
LNR005 Linear Scleroderma 23 0.031
956
HYP018 Hyperglobulinemic Purpura 22 0.031
957
P ACQ041 Acquired Amegakaryocytic Thrombocytopenia 21 0.031
958
c NPH107 Nephrotic Syndrome, Type 19 21 0.031
959
MTR027 Mitral Atresia 20 0.031
960
AND005 Androgen Insensitivity Syndrome, Mild 19 0.031
961
EPS047 Epstein-Barr Virus-Associated Malignant Lymphoproliferative Disorder 18 0.031
962
HHV001 Hhv-6 Encephalitis 18 0.031
963
ANT063 Anti-P200 Pemphigoid 17 0.031
964
ORB010 Orbital Granuloma 17 0.031
965
BLD137 Blood Group--Ahonen 16 0.031
966
c PSD024 Pseudo Pelger-Huet Anomaly 13 0.031
967
OBS524 Obsolete: Benign Exophthalmos Syndrome 13 0.031
968
ERY018 Erythema Nodosum, Idiopathic 10 0.031
969
IMM215 Immunodeficiency-Associated Lymphoproliferative Disease 8 0.031
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