Search results for Mycophenolate mofetil

986 hits were found for Mycophenolate mofetil

# Family MCID Name MIFTS Score
1
MYC060 Mycophenolate Mofetil Embryopathy 19 4.196
2
c SYS001 Systemic Lupus Erythematosus 86 0.618
3
P GRF003 Graft-Versus-Host Disease 72 0.608
4
P LPS004 Lupus Erythematosus 61 0.533
5
P LKM002 Leukemia 68 0.447
6
c ACT135 Acute Graft Versus Host Disease 52 0.416
7
P LYM118 Lymphoma 68 0.416
8
LYM019 Lymphosarcoma 46 0.408
9
P KDN018 Kidney Disease 72 0.401
10
MYL009 Myelodysplastic Syndrome 70 0.396
11
P MYL006 Myeloid Leukemia 60 0.395
12
P NTR004 Neutropenia 63 0.371
13
c LKM061 Leukemia, Acute Myeloid 84 0.365
14
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.351
15
P LKM062 Leukemia, Acute Lymphoblastic 69 0.350
16
P GLM007 Glomerulonephritis 57 0.347
17
HMT002 Hematologic Cancer 62 0.345
18
P NPH012 Nephrotic Syndrome 60 0.342
19
ATM095 Autoimmune Disease 62 0.339
20
LYM040 Lymphoblastic Lymphoma 54 0.331
21
c LKM063 Leukemia, Chronic Myeloid 72 0.330
22
HML018 Homologous Wasting Disease 22 0.330
23
P LKM071 Leukemia, Chronic Lymphocytic 79 0.321
24
LYM133 Lymphoma, Hodgkin, Classic 69 0.315
25
END086 End Stage Renal Disease 51 0.314
26
MYL069 Myeloma, Multiple 85 0.312
27
c CHR417 Chronic Graft Versus Host Disease 57 0.309
28
PLS009 Plasma Cell Neoplasm 51 0.308
29
c PRM038 Primary Agammaglobulinemia 44 0.299
30
DFC004 Deficiency Anemia 70 0.299
31
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.299
32
c CHR064 Chronic Monocytic Leukemia 33 0.296
33
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.294
34
P BCL017 B-Cell Lymphoma 58 0.287
35
P VSC011 Vasculitis 62 0.285
36
P DRR001 Diarrhea 55 0.285
37
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.281
38
ADL002 Adult Syndrome 70 0.273
39
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.271
40
MNT001 Mantle Cell Lymphoma 69 0.266
41
P FLL037 Follicular Lymphoma 67 0.256
42
c FLL041 Follicular Lymphoma 1 49 0.256
43
CYT008 Cytomegalovirus Infection 57 0.256
44
P CNR004 Cone-Rod Dystrophy 2 73 0.254
45
LNG099 Lung Disease 60 0.254
46
IGG001 Iga Glomerulonephritis 48 0.244
47
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.243
48
MYL031 Myeloproliferative Neoplasm 66 0.242
49
BRK010 Burkitt Lymphoma 67 0.242
50
BNM001 Bone Marrow Cancer 43 0.240
51
P SRC025 Sarcoidosis 1 70 0.233
52
c SCL052 Scleroderma, Familial Progressive 61 0.233
53
P CHR285 Chronic Myelomonocytic Leukemia 60 0.232
54
INT066 Interstitial Lung Disease 60 0.230
55
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.230
56
MRG003 Marginal Zone B-Cell Lymphoma 52 0.228
57
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.228
58
PLS025 Plasmablastic Lymphoma 47 0.227
59
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.227
60
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.225
61
P PMP001 Pemphigus 54 0.221
62
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.218
63
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.217
64
c ACT073 Acute Leukemia 58 0.215
65
P MMB011 Membranous Nephropathy 50 0.212
66
c HYP595 Hypertension, Essential 84 0.211
67
48X005 48,xyyy 39 0.210
68
P MYS003 Myasthenia Gravis 68 0.210
69
WLD007 Waldenstroem's Macroglobulinemia 61 0.209
70
MCR004 Macroglobulinemia 49 0.209
71
LYM012 Lymphoplasmacytic Lymphoma 47 0.209
72
c RHB024 Rhabdomyosarcoma 2 67 0.209
73
c CHR684 Chronic Kidney Disease 70 0.208
74
c ATM011 Autoimmune Hepatitis 63 0.208
75
MYL005 Myelofibrosis 70 0.202
76
P SYS005 Systemic Scleroderma 68 0.202
77
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.201
78
P LYM033 Lymphoproliferative Syndrome 59 0.197
79
P UVT001 Uveitis 57 0.197
80
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.194
81
HDG004 Hodgkin's Granuloma 23 0.194
82
HDG006 Hodgkin's Paragranuloma 22 0.194
83
BLL006 Bullous Pemphigoid 62 0.194
84
P PSR002 Psoriasis 62 0.192
85
PST011 Pustulosis of Palm and Sole 52 0.192
86
RFR010 Refractory Anemia 48 0.191
87
P FCL005 Focal Segmental Glomerulosclerosis 57 0.191
88
c SYS043 Systemic Lupus Erythematosus 1 38 0.185
89
P HPT021 Hepatitis 67 0.183
90
MYC006 Mycosis Fungoides 66 0.181
91
SZR001 Sezary's Disease 60 0.181
92
FNG017 Fungal Infectious Disease 53 0.181
93
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.181
94
c LKM005 Leukemia, T-Cell, Chronic 34 0.181
95
P THR014 Thrombocytopenia 67 0.181
96
PRP030 Purpura 54 0.180
97
PMP006 Pemphigus Vulgaris, Familial 57 0.179
98
CYT002 Cytokine Deficiency 42 0.179
99
DRM006 Dermatitis 61 0.174
100
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.171
101
SPL004 Splenic Marginal Zone Lymphoma 51 0.171
102
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.171
103
DFF005 Diffuse Large B-Cell Lymphoma 55 0.168
104
P TRN020 Turner Syndrome 67 0.166
105
CLT003 Colitis 62 0.165
106
P ADL017 Adult T-Cell Leukemia 56 0.165
107
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.165
108
IDP091 Idiopathic Nephrotic Syndrome 42 0.165
109
P LVR013 Liver Disease 68 0.162
110
LYM051 Lymphomatoid Granulomatosis 45 0.162
111
PRL017 Prolymphocytic Leukemia 47 0.161
112
P DRM010 Dermatomyositis 61 0.160
113
P DRM053 Dermatitis, Atopic 66 0.160
114
IMM167 Immune Deficiency Disease 78 0.157
115
RTC005 Reticulosarcoma 47 0.156
116
CNN005 Connective Tissue Disease 68 0.156
117
SKN016 Skin Disease 63 0.156
118
P APL001 Aplastic Anemia 74 0.155
119
CHL149 Childhood Acute Myeloid Leukemia 44 0.155
120
NTR005 Nutritional Deficiency Disease 62 0.155
121
ANC002 Anca-Associated Vasculitis 41 0.155
122
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.154
123
ATY042 Atypical Chronic Myeloid Leukemia 49 0.153
124
HRP004 Herpes Zoster 60 0.153
125
c HPT001 Hepatitis C 62 0.150
126
HRY003 Hairy Cell Leukemia 55 0.150
127
MCS002 Mucositis 56 0.150
128
DFF003 Diffuse Scleroderma 41 0.150
129
c CHR418 Chronic Leukemia 49 0.148
130
P DBT009 Diabetes Mellitus 64 0.146
131
GLM044 Glomerular Disease 37 0.146
132
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.145
133
P CTN015 Cutaneous T Cell Lymphoma 49 0.145
134
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.145
135
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.144
136
ADR007 Adrenoleukodystrophy 75 0.143
137
BRN002 Bronchiolitis 59 0.142
138
c MCR113 Microvascular Complications of Diabetes 3 52 0.142
139
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.142
141
BRN012 Bronchiolitis Obliterans 55 0.139
142
P MLT020 Multiple Sclerosis 72 0.135
143
P IGN003 Iga Nephropathy 1 49 0.135
144
CRH001 Crohn's Disease 74 0.135
145
P PRL003 Proliferative Glomerulonephritis 44 0.135
146
PRP036 Peripheral T-Cell Lymphoma 53 0.134
147
ATM052 Autoimmune Disease 1 37 0.133
148
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.133
149
P PNM007 Pneumonia 68 0.133
150
LVR012 Liver Cirrhosis 62 0.133
151
P INF037 Inflammatory Bowel Disease 54 0.133
152
P PLM036 Pulmonary Fibrosis 65 0.133
153
MCR088 Microscopic Polyangiitis 51 0.132
154
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.132
155
PST046 Post-Transplant Lymphoproliferative Disease 53 0.131
156
c ACT071 Acute Kidney Failure 60 0.128
157
PLS016 Plasma Cell Leukemia 53 0.126
158
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.126
159
c MCR120 Microvascular Complications of Diabetes 7 47 0.124
160
c MCR130 Microvascular Complications of Diabetes 6 41 0.124
161
c MCR133 Microvascular Complications of Diabetes 4 41 0.124
162
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.124
163
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.124
164
GRN037 Granulomatosis with Polyangiitis 65 0.122
165
P PLY041 Polymyositis 57 0.122
166
FRY002 Fryns Syndrome 43 0.122
167
CHC001 Chickenpox 60 0.122
168
P EXN002 Exanthem 57 0.122
169
ATH013 Atherosclerosis Susceptibility 65 0.121
170
P HML002 Hemolytic Anemia 63 0.120
171
PYD001 Pyoderma Gangrenosum 54 0.120
172
PYD002 Pyoderma 50 0.120
173
PLY001 Polycythemia Vera 69 0.119
174
P PLY018 Polycythemia 56 0.119
175
c PRM012 Primary Polycythemia 50 0.119
176
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.119
177
CHR286 Chronic Neutrophilic Leukemia 42 0.119
178
LRG008 Large Granular Lymphocyte Leukemia 41 0.119
179
c FML035 Familial Hyperlipidemia 55 0.119
180
MMB001 Membranoproliferative Glomerulonephritis 55 0.119
181
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.118
182
c HPT073 Hepatitis C Virus 72 0.117
183
NRM001 Neuromyelitis Optica 61 0.117
184
c DRR009 Diarrhea 6 46 0.117
185
P ESS003 Essential Thrombocythemia 68 0.115
186
c THR090 Thrombocythemia 1 49 0.115
187
INT054 Intraocular Lymphoma 48 0.115
188
LPD008 Lipid Metabolism Disorder 62 0.114
189
c HPT016 Hepatitis B 59 0.114
190
ATX019 Ataxia with Vitamin E Deficiency 42 0.113
191
HMN044 Human Immunodeficiency Virus Type 1 71 0.112
192
P ALP008 Alopecia 54 0.112
193
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.110
194
MXD050 Mixed Phenotype Acute Leukemia 43 0.110
195
c DBT099 Diabetes Mellitus, Type I 65 0.110
196
P SCK005 Sickle Cell Disease 50 0.108
197
c HYP836 Hypercholesterolemia, Familial, 1 73 0.108
198
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.108
199
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.106
200
P CRD246 Cardiovascular System Disease 57 0.106
201
CHR563 Chronic Eosinophilic Leukemia 48 0.106
202
HYP066 Hyperglycemia 61 0.106
203
P CYS018 Cystitis 59 0.106
204
P RNL015 Renal Hypertension 47 0.106
205
c HPT003 Hepatitis a 62 0.106
206
RNL077 Renal Fibrosis 47 0.105
207
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.105
208
SCK003 Sickle Cell Anemia 74 0.104
209
P PRM006 Primary Biliary Cirrhosis 62 0.104
210
EYD002 Eye Disease 58 0.104
211
P MYS005 Myositis 56 0.104
212
HYP014 Hyperuricemia 52 0.104
213
P CHL066 Cholangitis 51 0.104
214
P ART022 Arthritis 69 0.104
215
c ACT068 Acute Cystitis 63 0.104
216
IDP011 Idiopathic Interstitial Pneumonia 59 0.103
217
P MYP004 Myopathy 70 0.102
218
P KDN017 Kidney Cancer 60 0.102
219
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.101
220
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.101
221
MCR103 Microtia 43 0.101
222
c LCL006 Localized Scleroderma 62 0.101
223
CHL079 Children's Interstitial Lung Disease 26 0.101
224
VRL011 Viral Infectious Disease 61 0.100
225
P ART021 Arteriosclerosis 54 0.099
226
P TRM003 Tremor 54 0.099
227
SPR126 Superior Semicircular Canal Dehiscence 40 0.099
228
c HMG029 Hemoglobin Se Disease 39 0.099
229
P RHM011 Rheumatoid Arthritis 80 0.099
230
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.097
231
AMN001 Amenorrhea 54 0.097
232
RTR011 Retroperitoneal Fibrosis 40 0.097
233
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.097
234
P BND020 Bone Disease 59 0.097
235
PNC001 Pancytopenia 54 0.097
236
ISC004 Ischemia 58 0.096
237
LYM027 Lymphopenia 58 0.096
238
c INT064 Intermediate Uveitis 55 0.096
239
P AMY004 Amyloidosis 70 0.094
240
P THL005 Thalassemia 60 0.094
241
PNM001 Pneumocystosis 59 0.094
242
P ANP001 Anaplastic Large Cell Lymphoma 58 0.094
243
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.094
244
IMM136 Immune System Disease 45 0.094
245
LTH001 Lethal Midline Granuloma 44 0.094
246
PMP004 Pemphigus Foliaceus 43 0.094
247
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.094
248
P PNV001 Panuveitis 50 0.094
249
P NRB001 Neuroblastoma 72 0.093
250
CNS004 Constipation 58 0.092
251
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.092
252
P EPD016 Epidermolysis Bullosa 53 0.092
253
P SCL015 Scleritis 48 0.092
254
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.091
255
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.089
256
c ALP101 Alpha-Thalassemia 62 0.089
257
ALL026 Allergic Hypersensitivity Disease 62 0.089
258
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.089
259
CLF001 Cleft Lip 53 0.089
260
THR004 Thrombocytosis 51 0.089
261
c ALM001 Al Amyloidosis 50 0.089
262
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.089
263
RDC006 Red Cell Aplasia 43 0.089
264
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.089
265
P RSP003 Respiratory Failure 74 0.089
266
OCL020 Ocular Cicatricial Pemphigoid 55 0.089
267
DWN001 Down Syndrome 70 0.086
268
c ANM038 Anemia, Autoimmune Hemolytic 62 0.086
269
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.086
270
PPT005 Peptic Ulcer Disease 59 0.086
271
BCT022 Bacterial Infectious Disease 56 0.086
272
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.086
273
P CTN003 Cutaneous Lupus Erythematosus 53 0.086
274
CYS001 Cystic Fibrosis 81 0.085
275
KPS004 Kaposi Sarcoma 75 0.084
276
HMG005 Hemoglobinopathy 56 0.084
277
c PST005 Posterior Uveitis 54 0.084
278
P HML001 Hemolytic-Uremic Syndrome 53 0.084
279
c INF145 Infantile Liver Failure Syndrome 1 50 0.084
280
c NPH049 Nephrotic Syndrome, Type 2 48 0.084
281
CLS052 Classic Hairy Cell Leukemia 27 0.084
282
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.083
283
CLF004 Cleft Lip/palate 54 0.081
284
P MST002 Mast-Cell Leukemia 49 0.081
285
P SCL009 Sclerosing Cholangitis 48 0.081
286
P PRR002 Pure Red-Cell Aplasia 47 0.081
287
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.081
288
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.081
289
P ESP024 Esophagitis 62 0.081
290
P ENC004 Encephalitis 61 0.081
291
ERY051 Erythroleukemia, Familial 56 0.081
292
LYM005 Lymphocele 35 0.081
293
c PSR017 Psoriasis 2 53 0.080
294
c PSR023 Psoriasis 1 52 0.080
295
c PSR032 Psoriasis 11 47 0.080
296
c PSR028 Psoriasis 7 42 0.080
297
c PSR018 Psoriasis 13 41 0.080
298
c FNC027 Fanconi Anemia, Complementation Group a 81 0.078
299
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.078
300
ALS001 Alstrom Syndrome 64 0.078
301
CHR001 Churg-Strauss Syndrome 61 0.078
302
P PNC044 Pancreatitis 61 0.078
303
ACQ007 Acquired Immunodeficiency Syndrome 60 0.078
304
P MYC008 Myocarditis 59 0.078
305
PLS011 Plasmacytoma 56 0.078
306
c ACT134 Acute Liver Failure 56 0.078
307
P LCH002 Lichen Planus 53 0.078
308
P FNC004 Fanconi Syndrome 50 0.078
309
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.078
310
RFR002 Refractory Hairy Cell Leukemia 33 0.078
311
SVR004 Severe Combined Immunodeficiency 73 0.077
312
P HYP098 Hypereosinophilic Syndrome 67 0.077
313
c BKV001 Bk-Virus Nephropathy 24 0.077
314
SCH036 Scheie Syndrome 72 0.076
315
P SKN015 Skin Carcinoma 66 0.076
316
P VSC007 Vascular Disease 63 0.076
317
ULC004 Ulcerative Colitis 73 0.075
318
HYP056 Hypoglycemia 66 0.075
319
P URT039 Urticaria 58 0.075
320
CLB010 Coloboma of Macula 52 0.075
321
INT067 Interstitial Nephritis 48 0.075
322
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.075
323
FBR089 Fibrosclerosis, Multifocal 38 0.075
324
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.075
325
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.075
326
P HYP750 Hypertriglyceridemia, Familial 62 0.075
327
VSL002 Visual Epilepsy 59 0.075
328
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.075
329
P SZR006 Seizure Disorder 56 0.075
330
ACT058 Active Peptic Ulcer Disease 55 0.075
331
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.075
332
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.075
333
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.075
334
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.075
335
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.075
336
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.075
337
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.075
338
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.075
339
ACT003 Acute Kidney Tubular Necrosis 45 0.075
340
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.075
341
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.075
342
CCT002 Cicatricial Pemphigoid 51 0.074
343
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.074
344
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.072
345
c NRF023 Neurofibromatosis, Type Ii 80 0.072
346
P HRT032 Heart Disease 75 0.072
347
c BTT014 Beta-Thalassemia 74 0.072
348
MGK001 Megakaryocytic Leukemia 64 0.072
349
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.072
350
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.072
351
c LKM070 Leukemia, Acute Monocytic 57 0.072
352
ENT011 Enterocolitis 51 0.072
353
CYS036 Cystinosis, Nephropathic 51 0.072
354
HMG002 Hemoglobinuria 50 0.072
355
EPD006 Epidermolysis Bullosa Acquisita 49 0.072
357
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.072
358
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.072
359
P FNC034 Fanconi Renotubular Syndrome 2 40 0.072
360
PLY043 Polyomavirus Allograft Nephropathy 13 0.072
361
NRM005 Neuromuscular Disease 64 0.071
362
CHL068 Cholestasis 61 0.071
363
IRN002 Iron Metabolism Disease 57 0.071
364
THR024 Thrombosis 57 0.071
365
P GST044 Gastritis 56 0.071
366
P MCR115 Microvascular Complications of Diabetes 5 66 0.069
367
ERY003 Erythema Multiforme 58 0.069
368
c CHL119 Cholangitis, Primary Sclerosing 57 0.069
369
P ANT006 Antiphospholipid Syndrome 55 0.069
370
P CNT005 Central Nervous System Lymphoma 53 0.069
371
PNN001 Panniculitis 51 0.069
372
47X002 47,xyy 49 0.069
373
c INH020 Inherited Metabolic Disorder 47 0.069
374
URT010 Ureteral Obstruction 45 0.069
375
P MNN013 Meningitis 66 0.068
376
P CTR002 Cataract 60 0.068
377
P NRP001 Neuropathy 56 0.068
378
P PLY019 Polyneuropathy 56 0.068
379
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.068
380
P PNC035 Pancreatic Cancer 84 0.065
381
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.065
382
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.065
383
P AGM001 Agammaglobulinemia 65 0.065
384
SRC014 Sarcoma 65 0.065
385
P CRN300 Coronary Heart Disease 1 63 0.065
386
TKY002 Takayasu Arteritis 62 0.065
387
LPP008 Lipoprotein Quantitative Trait Locus 62 0.065
388
c ACT027 Acute Pancreatitis 60 0.065
389
P BRN022 Bronchiectasis 59 0.065
390
P PLY017 Polyarteritis Nodosa 58 0.065
391
EXT034 Extrinsic Allergic Alveolitis 58 0.065
392
P INF032 Infertility 57 0.065
393
BLR008 Bilirubin Metabolic Disorder 57 0.065
394
HNC001 Henoch-Schoenlein Purpura 55 0.065
395
P MNC007 Monocytic Leukemia 53 0.065
396
SPN035 Spindle Cell Sarcoma 53 0.065
397
DMY004 Demyelinating Disease 52 0.065
398
ACR041 Acromelic Frontonasal Dysostosis 52 0.065
399
HYP081 Hypolipoproteinemia 51 0.065
400
CMB003 Combined T Cell and B Cell Immunodeficiency 49 0.065
401
HST010 Histiocytosis 48 0.065
402
P PLY020 Polyradiculoneuropathy 48 0.065
403
CRS001 Crescentic Glomerulonephritis 43 0.065
404
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.065
405
THR123 Thrombotic Microangiopathy 36 0.065
406
CMB081 Combined Immunodeficiency, X-Linked 36 0.065
407
ALL012 Allergic Angiitis 24 0.065
409
STR067 Stroke, Ischemic 81 0.064
410
CRB039 Cerebrovascular Disease 67 0.064
411
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.064
412
c FNC043 Fanconi Anemia, Complementation Group E 62 0.062
413
c MCR129 Microvascular Complications of Diabetes 1 66 0.061
414
CLF027 Cleft Palate, Isolated 64 0.061
415
ACT119 Acute Promyelocytic Leukemia 63 0.061
416
P INT143 Interstitial Cystitis 61 0.061
417
ADL030 Adult-Onset Still's Disease 58 0.061
418
CHL028 Childhood Type Dermatomyositis 58 0.061
419
P PYL005 Pyelonephritis 56 0.061
420
MCL006 Macular Retinal Edema 55 0.061
421
HYP748 Hypertelorism 50 0.061
422
FRN020 Frontal Fibrosing Alopecia 49 0.061
423
EVN001 Evans' Syndrome 48 0.061
424
c PRM226 Primary Central Nervous System Lymphoma 48 0.061
425
ANT039 Antisynthetase Syndrome 46 0.061
426
C3G002 C3 Glomerulopathy 45 0.061
427
c MCR112 Microvascular Complications of Diabetes 2 41 0.061
428
NDL003 Nodular Nonsuppurative Panniculitis 39 0.061
429
NRS005 Neurosarcoidosis 36 0.061
430
c PRM039 Primary Angiitis of the Central Nervous System 33 0.061
431
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 19 0.061
432
P BRS047 Breast Cancer 97 0.061
433
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.061
434
P HRP006 Herpes Simplex 65 0.061
435
CLN015 Colon Adenocarcinoma 65 0.061
436
ESP020 Esophageal Atresia 62 0.061
437
P ENC018 Encephalopathy 61 0.061
438
SQM006 Squamous Cell Carcinoma 60 0.061
439
P OPT006 Optic Nerve Disease 60 0.061
440
DYS073 Dysphagia 50 0.061
441
ACT029 Acute Interstitial Pneumonia 49 0.061
442
HMR023 Hemorrhagic Cystitis 45 0.061
443
SYS071 Systemic Autoimmune Disease 37 0.061
444
P HPT023 Hepatocellular Carcinoma 100 0.059
445
P PRS040 Prostate Cancer 97 0.057
446
P WSK001 Wiskott-Aldrich Syndrome 72 0.057
447
P DMN001 Diamond-Blackfan Anemia 69 0.057
448
P MLN008 Melanoma 69 0.057
449
SKN019 Skin Melanoma 68 0.057
450
P INF038 Influenza 68 0.057
451
P DYS007 Dyskeratosis Congenita 67 0.057
452
P CHR012 Chronic Granulomatous Disease 67 0.057
453
DGR001 Digeorge Syndrome 64 0.057
454
PSR001 Psoriatic Arthritis 61 0.057
455
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.057
456
PRT013 Portal Hypertension 59 0.057
457
INC002 Inclusion Body Myositis 58 0.057
458
LNG108 Langerhans Cell Histiocytosis 58 0.057
459
P HDC001 Headache 57 0.057
460
HPT046 Hepatic Veno-Occlusive Disease 56 0.057
461
VLC001 Velocardiofacial Syndrome 54 0.057
462
PPL022 Papilloma 54 0.057
463
HYP063 Hypersplenism 53 0.057
464
ACT200 Acute Monoblastic Leukemia 52 0.057
465
GNG012 Gingival Overgrowth 51 0.057
466
P HYP077 Hypertrichosis 50 0.057
467
ENT004 Enthesopathy 49 0.057
468
ACT098 Acute Erythroid Leukemia 48 0.057
469
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.057
470
MLT075 Multifocal Motor Neuropathy 46 0.057
471
SQM002 Squamous Cell Papilloma 46 0.057
472
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.057
473
CVD001 Covid-19 44 0.057
474
IDP033 Idiopathic Edema 44 0.057
475
P DMY001 Demyelinating Polyneuropathy 43 0.057
476
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.057
477
c CHR682 Chronic Bilirubin Encephalopathy 39 0.057
478
CHR463 Chronic Actinic Dermatitis 37 0.057
479
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.057
480
FML285 Familial Apolipoprotein C-Ii Deficiency 29 0.057
481
HRP008 Herpes Simiae 25 0.057
482
c ADL093 Adult Acute Monocytic Leukemia 20 0.057
483
MSC007 Muscle Hypertrophy 64 0.056
484
P SJG008 Sjogren Syndrome 61 0.056
485
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.056
486
KRT006 Keratoconjunctivitis 53 0.056
487
KRT001 Keratoconjunctivitis Sicca 49 0.056
488
URM002 Uremia 49 0.056
489
LPD004 Lipoid Nephrosis 46 0.056
491
c THR092 Thrombophilia Due to Thrombin Defect 73 0.053
492
P MTC003 Metachromatic Leukodystrophy 70 0.053
493
P KRB001 Krabbe Disease 69 0.053
494
c HYP768 Hyperlipoproteinemia, Type I 67 0.053
495
P NRV007 Nervous System Disease 66 0.053
496
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.053
497
P LKD001 Leukodystrophy 59 0.053
498
c CHL140 Chilblain Lupus 1 58 0.053
499
c CNT035 Central Nervous System Disease 52 0.053
500
P PLG001 Pelger-Huet Anomaly 51 0.053
501
FML026 Familial Lipoprotein Lipase Deficiency 51 0.053
502
MYL001 Myelitis 51 0.053
503
STM007 Stomatitis 50 0.053
504
PRX001 Peroxisomal Disease 46 0.053
505
ISC015 Ischemic Colitis 44 0.053
506
MNT303 Mental Retardation, X-Linked, Syndromic, Cabezas Type 41 0.053
507
ADR022 Adrenomyeloneuropathy 38 0.053
508
RFR004 Refractory Hematologic Cancer 30 0.053
509
SYN092 Syndromic X-Linked Intellectual Disability Cabezas Type 28 0.053
510
P OVR096 Overlap Myositis 27 0.053
511
GLS018 Glass Syndrome 57 0.052
513
P OST002 Osteoporosis 74 0.052
514
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.052
515
P PLY014 Polycystic Kidney Disease 62 0.052
516
P ALP009 Alopecia Areata 60 0.052
517
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.052
518
HYP005 Hypokalemia 55 0.052
519
GST037 Gastroparesis 54 0.052
520
CRH005 Crohn's Colitis 53 0.052
521
TXC002 Toxic Encephalopathy 53 0.052
522
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.052
523
MYL020 Myelomeningocele 51 0.052
524
DDN006 Duodenitis 49 0.052
525
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.052
526
c ATM099 Autoimmune Uveitis 45 0.052
527
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.052
528
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.052
529
ALL014 Allergic Encephalomyelitis 38 0.052
530
P PLY188 Polyendocrinopathy 32 0.052
531
MRF001 Marfan Syndrome 77 0.048
532
CRV035 Cervical Cancer 76 0.048
533
c SPN225 Spondyloarthropathy 1 73 0.048
534
P ASP006 Aspergillosis 69 0.048
535
P CRN037 Craniosynostosis 68 0.048
536
P MYC084 Mycobacterium Tuberculosis 1 68 0.048
537
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.048
538
FCT007 Factor Vii Deficiency 67 0.048
539
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.048
540
PRT037 Pertussis 65 0.048
541
HRL003 Hurler Syndrome 65 0.048
542
P THY023 Thymoma 65 0.048
543
PRT036 Peritonitis 64 0.048
544
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.048
545
P RHB003 Rhabdomyosarcoma 63 0.048
546
c PRC016 Pre-Eclampsia 63 0.048
547
OST003 Osteonecrosis 61 0.048
548
ALC006 Alcoholic Hepatitis 61 0.048
549
P TST021 Testicular Germ Cell Tumor 60 0.048
550
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.048
551
HYD002 Hydronephrosis 60 0.048
552
VGN017 Vaginal Cancer 60 0.048
553
DYS164 Dyskeratosis Congenita, X-Linked 60 0.048
554
P URF003 Urofacial Syndrome 1 57 0.048
555
AYM001 Ayme-Gripp Syndrome 57 0.048
556
PGM001 Pigmented Villonodular Synovitis 56 0.048
557
PRN038 Prune Belly Syndrome 56 0.048
558
MRD002 Marden-Walker Syndrome 56 0.048
559
VGT001 Vogt-Koyanagi-Harada Disease 55 0.048
560
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.048
561
URN010 Urinary Tract Obstruction 55 0.048
562
BRN014 Bronchopneumonia 54 0.048
563
c DMN023 Diamond-Blackfan Anemia 1 53 0.048
564
IRD001 Iridocyclitis 53 0.048
565
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.048
566
c VRL010 Viral Hepatitis 52 0.048
567
CRT016 Carotid Artery Disease 52 0.048
568
ART140 Arteries, Anomalies of 52 0.048
569
c THY107 Thymoma, Familial 52 0.048
570
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 51 0.048
571
P SPP010 Suppressor of Tumorigenicity 3 51 0.048
572
ATS010 Autosomal Recessive Disease 48 0.048
573
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.048
574
URN009 Urinary System Disease 48 0.048
575
ADN001 Adenosine Deaminase Deficiency 47 0.048
576
KRT008 Keratopathy 47 0.048
577
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.048
578
RTN023 Retinitis 46 0.048
579
GST010 Gestational Trophoblastic Neoplasm 46 0.048
580
EXT010 Extramedullary Plasmacytoma 45 0.048
581
c ACQ014 Acquired Hemophilia 45 0.048
582
GRN017 Granulocytopenia 44 0.048
583
c HYP272 Hypercholesterolemia, Familial, 3 44 0.048
584
P TST026 Testicular Germ Cell Cancer 43 0.048
585
NRR001 Neuroretinitis 42 0.048
586
c PST041 Posterior Urethral Valves 41 0.048
587
49X006 49, Xxxxy Syndrome 41 0.048
588
LNR006 Linear Iga Disease 40 0.048
589
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.048
590
P BCL005 B Cell Prolymphocytic Leukemia 39 0.048
591
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.048
592
OVR094 Ovarian Epithelial Cancer 38 0.048
593
TRP005 Trophoblastic Neoplasm 38 0.048
594
c ATM045 Autoimmune Glomerulonephritis 36 0.048
595
GRM010 Germ Cells Tumors 34 0.048
596
LTT002 Letterer-Siwe Disease 33 0.048
597
GNT019 Giant Cell Myocarditis 30 0.048
598
c TST046 Testicular Germ Cell Tumor 1 29 0.048
599
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.048
600
MLG164 Malignant Epithelial Tumor of Ovary 26 0.048
601
PLY179 Polyomavirus-Associated Nephropathy 24 0.048
603
P MYC007 Myocardial Infarction 70 0.046
604
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.046
605
c SVR001 Severe Acute Respiratory Syndrome 62 0.046
606
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.046
607
PLM012 Pulmonary Sarcoidosis 53 0.046
608
P FML011 Familial Adenomatous Polyposis 72 0.043
609
SVR097 Severe Cutaneous Adverse Reaction 69 0.043
610
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.043
611
P TYS001 Tay-Sachs Disease 69 0.043
612
SND001 Sandhoff Disease 68 0.043
613
BRN024 Bronchitis 68 0.043
614
PNC129 Pancreatic Adenocarcinoma 68 0.043
615
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.043
616
P CLC063 Celiac Disease 1 66 0.043
617
LYS012 Lysosomal Acid Lipase Deficiency 65 0.043
618
c MCP001 Mucopolysaccharidosis Iii 65 0.043
619
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.043
620
c JVN010 Juvenile Rheumatoid Arthritis 64 0.043
621
c DPH024 Diaphragmatic Hernia, Congenital 63 0.043
622
c GM1007 Gm1 Gangliosidosis 62 0.043
623
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.043
624
c JVN061 Juvenile Arthritis 60 0.043
625
P TXP001 Toxoplasmosis 60 0.043
626
STT001 Status Epilepticus 60 0.043
627
PLM033 Pulmonary Embolism 59 0.043
628
MCR013 Microphthalmia 57 0.043
629
CMR002 Coumarin Resistance 56 0.043
630
MCR141 Mucormycosis 56 0.043
631
GDP001 Goodpasture Syndrome 55 0.043
632
c ATM024 Autoimmune Pancreatitis 55 0.043
633
CLR030 Clear Cell Renal Cell Carcinoma 53 0.043
634
INT051 Intussusception 53 0.043
635
SPN051 Spondylitis 51 0.043
636
P HMP007 Hemophilia 51 0.043
637
OCL069 Ocular Motor Apraxia 51 0.043
638
PLR008 Pleurisy 50 0.043
639
CRT013 Carotid Stenosis 50 0.043
640
FSC004 Fasciitis 50 0.043
641
BLR001 Biliary Atresia 50 0.043
642
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.043
643
MNN009 Meningoencephalitis 49 0.043
644
CRY004 Cryoglobulinemia 48 0.043
645
SPL018 Splenomegaly 48 0.043
646
P MCL001 Mucolipidosis 48 0.043
647
CLL014 Cll/sll 45 0.043
648
CNT046 Central Nervous System Vasculitis 44 0.043
649
P GNG009 Gangliosidosis 44 0.043
650
MGS001 Megaesophagus 43 0.043
651
PRN049 Paraneoplastic Pemphigus 42 0.043
652
DSC009 Discoid Lupus Erythematosus 42 0.043
653
OBS082 Obstructive Nephropathy 42 0.043
654
RDN001 Reading Disorder 40 0.043
655
CRN020 Coronary Restenosis 39 0.043
656
ERM002 Ear Malformation 39 0.043
657
CRB001 Cerebral Lymphoma 39 0.043
658
CFH006 Cfhr5 Deficiency 37 0.043
659
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.043
660
LYM043 Lymphocytic Hypophysitis 32 0.043
661
INF009 Inflammatory Spondylopathy 31 0.043
662
ERY066 Erythema Multiforme Major 30 0.043
663
IGP001 Iga Pemphigus 26 0.043
664
NRL016 Neural Tube Defects 82 0.042
665
CMM004 Common Variable Immunodeficiency 68 0.042
666
c INF071 Inflammatory Bowel Disease 1 67 0.042
667
OST159 Osteogenic Sarcoma 66 0.042
668
P HYP069 Hyperparathyroidism 63 0.042
669
GST050 Gastrointestinal System Disease 56 0.042
670
PTT041 Pituitary Stalk Interruption Syndrome 50 0.042
671
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.042
672
CRD043 Ceroid Storage Disease 44 0.042
673
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.042
674
PLY021 Polyradiculopathy 41 0.042
675
c ACT004 Acute Diarrhea 39 0.042
676
CDQ001 Cauda Equina Syndrome 38 0.042
677
RFR013 Refractory Celiac Disease 35 0.042
678
SPT004 Septic Arthritis 58 0.037
679
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.037
680
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.037
681
c DLT002 Dilated Cardiomyopathy 79 0.037
682
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.037
683
PRP027 Peripheral Vascular Disease 71 0.037
684
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.037
685
MST024 Mastocytosis, Cutaneous 69 0.037
686
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.037
687
GST092 Gastroesophageal Reflux 67 0.037
688
P SHW006 Shwachman-Diamond Syndrome 1 67 0.037
689
P PLM037 Pulmonary Hypertension 67 0.037
690
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.037
691
CHD001 Chediak-Higashi Syndrome 66 0.037
692
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 0.037
693
P MTR014 Motor Neuron Disease 65 0.037
694
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.037
695
P MST009 Mastocytosis 64 0.037
696
GT001 Gout 64 0.037
697
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.037
698
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.037
699
TXC005 Toxic Shock Syndrome 62 0.037
700
ASP002 Aspartylglucosaminuria 62 0.037
701
MSL001 Measles 62 0.037
702
INT002 Intermittent Claudication 61 0.037
703
FCS002 Fucosidosis 61 0.037
704
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.037
705
PRT058 Pure Autonomic Failure 59 0.037
706
AVN001 Avian Influenza 59 0.037
707
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.037
708
CNT047 Contact Dermatitis 58 0.037
709
P MMP001 Mumps 58 0.037
710
P PRP019 Peripheral Nervous System Disease 58 0.037
711
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 0.037
712
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.037
713
PLY023 Polycystic Liver Disease 57 0.037
714
SKN022 Skin Squamous Cell Carcinoma 57 0.037
715
SFT003 Soft Tissue Sarcoma 56 0.037
716
ALL010 Allergic Contact Dermatitis 56 0.037
717
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.037
718
P HYP024 Hypoparathyroidism 56 0.037
719
HRL004 Hurler-Scheie Syndrome 55 0.037
720
GLC003 Glucose Intolerance 54 0.037
721
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.037
722
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.037
723
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.037
724
PRC013 Pericarditis 54 0.037
725
ANL018 Analbuminemia 54 0.037
726
RVS001 Revesz Syndrome 54 0.037
727
P LTR001 Lateral Sclerosis 54 0.037
728
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.037
729
c HPT007 Hepatitis E 53 0.037
730
EXP004 Exophthalmos 52 0.037
731
LYS002 Lysosomal Storage Disease 52 0.037
732
GLM004 Gliomatosis Cerebri 52 0.037
733
P THY032 Thyroiditis 52 0.037
734
ILS001 Ileus 51 0.037
735
P OVR082 Overgrowth Syndrome 50 0.037
736
HPT014 Hepatorenal Syndrome 50 0.037
737
CYT005 Cytomegalovirus Retinitis 50 0.037
738
MTB004 Metabolic Acidosis 50 0.037
739
c PSR021 Psoriasis 14, Pustular 50 0.037
740
MYL003 Myeloid Sarcoma 49 0.037
741
CGN006 Cogan Syndrome 48 0.037
742
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.037
743
CLC006 Calcinosis 48 0.037
744
BRD025 Birdshot Chorioretinopathy 48 0.037
745
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.037
746
BBS001 Babesiosis 48 0.037
747
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 48 0.037
748
SPH010 Sphingolipidosis 47 0.037
749
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.037
750
RYN005 Raynaud Phenomenon 47 0.037
751
HYR002 Hoyeraal Hreidarsson Syndrome 46 0.037
752
TCL003 T Cell Deficiency 46 0.037
753
ANR004 Anuria 46 0.037
754
c MYL058 Myeloproliferative Syndrome, Transient 44 0.037
755
KMR001 Kimura Disease 43 0.037
756
MST004 Mast Cell Neoplasm 42 0.037
757
TRP009 Triple X Syndrome 42 0.037
758
P PRT026 Parotitis 42 0.037
759
BCK006 Back Pain 42 0.037
760
ACT088 Acute Insulin Response 41 0.037
761
P MLG074 Malignant Mesenchymoma 40 0.037
762
THR035 Thrombasthenia 40 0.037
763
LKP003 Leukoplakia 39 0.037
764
ENT001 Enterocele 39 0.037
765
ORL012 Oral Leukoplakia 39 0.037
766
EXT007 Extracutaneous Mastocytoma 38 0.037
767
MCP033 Mucopolysaccharidoses 38 0.037
768
P PST059 Pustular Psoriasis 37 0.037
769
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 37 0.037
770
TTH004 Tethered Spinal Cord Syndrome 35 0.037
771
ATY022 Atypical Coarctation of Aorta 34 0.037
772
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.037
773
P INH011 Inherited Bone Marrow Failure Syndromes 34 0.037
774
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.037
775
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.037
776
HDG005 Hodgkin's Lymphoma, Mixed Cellularity 30 0.037
777
MYC088 Mycobacterium Avium Complex Infections 29 0.037
778
CYT018 Cytochrome P450 2d6 Variant 27 0.037
779
PGM030 Pigmentation Anomaly of the Skin 26 0.037
780
c SYS066 Systemic Polyarteritis Nodosa 26 0.037
781
P PLM069 Pulmonary Venous Return Anomaly 26 0.037
782
HMP028 Hemophagocytic Syndrome Associated with an Infection 24 0.037
783
CHR208 Chromosome 17p Deletion 23 0.037
784
BLL015 Bullous Lichen Planus 21 0.037
785
PFF001 Pfeiffer Syndrome 79 0.031
786
CNN003 Conn's Syndrome 79 0.031
787
INS024 Insulin-Like Growth Factor I 79 0.031
788
P LNG064 Lung Cancer Susceptibility 3 78 0.031
789
c ATR087 Atrial Standstill 1 75 0.031
790
MSC157 Muscular Dystrophy, Duchenne Type 72 0.031
791
WLS001 Wilson Disease 71 0.031
792
GST040 Gastric Adenocarcinoma 70 0.031
793
P TTR001 Tetralogy of Fallot 70 0.031
794
CNG034 Congestive Heart Failure 69 0.031
795
P LPR021 Leprosy 3 69 0.031
796
P ALP004 Alport Syndrome 68 0.031
797
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.031
798
CHR103 Charge Syndrome 67 0.031
799
c HMP029 Hemophilia a 67 0.031
800
P MSC005 Muscular Dystrophy 66 0.031
801
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.031
802
LNG039 Lung Squamous Cell Carcinoma 66 0.031
803
KRT019 Keratitis, Hereditary 65 0.031
804
BRR014 Barrett Esophagus 65 0.031
805
P ANR048 Aniridia 1 63 0.031
806
PLG002 Plague 63 0.031
807
c HYP794 Hyperoxaluria, Primary, Type I 63 0.031
808
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.031
809
TRN015 Transient Cerebral Ischemia 63 0.031
810
ANR007 Anorexia Nervosa 63 0.031
811
DPR016 Depression 63 0.031
812
P ECT006 Ectodermal Dysplasia 62 0.031
813
P TRC086 Trichohepatoenteric Syndrome 1 62 0.031
814
P ART023 Arthropathy 62 0.031
815
HYD038 Hydrops Fetalis, Nonimmune 62 0.031
816
P PRM002 Primary Hyperoxaluria 62 0.031
817
CRC021 Carcinosarcoma 62 0.031
818
MDD011 Mood Disorder 62 0.031
819
c WLM018 Wilms Tumor 5 61 0.031
820
SDD001 Sudden Infant Death Syndrome 61 0.031
821
FBR086 Fibrolamellar Carcinoma 61 0.031
822
SPN186 Spinal Cord Injury 60 0.031
823
CRD223 Cardiac Arrhythmia 60 0.031
824
ACN002 Acanthosis Nigricans 60 0.031
825
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.031
826
P MCR010 Microcephaly 59 0.031
827
P GLL022 Guillain-Barre Syndrome 59 0.031
828
P INT070 Intestinal Obstruction 58 0.031
829
BRS051 Breast Disease 58 0.031
830
MNT002 Mental Depression 58 0.031
831
c DWL002 Dowling-Degos Disease 1 58 0.031
832
P CND004 Candidiasis 58 0.031
833
MXD005 Mixed Connective Tissue Disease 58 0.031
834
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.031
835
PLM070 Pulmonic Stenosis 57 0.031
836
DSS009 Disseminated Intravascular Coagulation 57 0.031
837
CPR004 Coproporphyria, Hereditary 57 0.031
838
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.031
839
INT303 Intracranial Hypertension, Idiopathic 57 0.031
840
LST001 Listeriosis 56 0.031
841
TRN018 Transitional Cell Carcinoma 56 0.031
842
DBL002 Double Outlet Right Ventricle 56 0.031
843
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.031
844
HMF006 Hemifacial Microsomia 55 0.031
845
c BCT007 Bacterial Meningitis 55 0.031
846
P DBT005 Diabetes Insipidus 55 0.031
847
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.031
848
HMP005 Hemiplegia 55 0.031
849
NCR004 Nocardiosis 54 0.031
850
RLP001 Relapsing Polychondritis 54 0.031
851
THR013 Thoracic Outlet Syndrome 54 0.031
852
PLM010 Pulmonary Edema 54 0.031
853
STF002 Stiff Skin Syndrome 54 0.031
854
PTT009 Pituitary Gland Disease 54 0.031
855
P RTN016 Retinal Degeneration 53 0.031
856
P PLM006 Pulmonary Alveolar Proteinosis 53 0.031
857
MST005 Mastitis 53 0.031
858
P SHR001 Short Bowel Syndrome 53 0.031
859
ERD001 Erdheim-Chester Disease 53 0.031
860
GST023 Gastric Ulcer 53 0.031
861
FRY006 Fryns Microphthalmia Syndrome 52 0.031
862
CHR073 Choreatic Disease 52 0.031
863
P DDN001 Duodenal Ulcer 52 0.031
864
LYM004 Lymphoid Interstitial Pneumonia 51 0.031
865
FDL002 Food Allergy 51 0.031
866
c PRM108 Primary Progressive Multiple Sclerosis 51 0.031
867
P PRC012 Pericardial Effusion 51 0.031
868
BLL003 Bell's Palsy 51 0.031
869
HYP074 Hypersensitivity Vasculitis 51 0.031
870
STR008 Strongyloidiasis 51 0.031
871
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.031
872
INT071 Intestinal Perforation 51 0.031
873
c PYR010 Peyronie's Disease 50 0.031
874
P ECL001 Eclampsia 50 0.031
875
c HRD202 Hereditary Lymphedema I 50 0.031
876
CHR078 Chorioretinitis 50 0.031
877
P TMP001 Temporal Lobe Epilepsy 50 0.031
878
PRT018 Portal Vein Thrombosis 50 0.031
879
ILT001 Ileitis 50 0.031
880
NPH010 Nephrosclerosis 50 0.031
881
RNL011 Renal Osteodystrophy 50 0.031
882
PPL021 Papilledema 49 0.031
883
CRP032 Corpus Callosum, Agenesis of 49 0.031
884
SCT005 Scott Syndrome 49 0.031
885
c BCT013 Bacterial Pneumonia 48 0.031
886
BNR002 Bone Resorption Disease 48 0.031
887
NCR007 Necrotizing Fasciitis 48 0.031
888
CRY014 Cryptococcal Meningitis 48 0.031
889
WTH001 Withdrawal Disorder 48 0.031
890
MCR020 Microsporidiosis 48 0.031
891
ASP007 Aspiration Pneumonia 48 0.031
892
HPT009 Hepatopulmonary Syndrome 48 0.031
893
HMP001 Hemopericardium 48 0.031
894
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.031
895
ESN015 Eosinophilic Fasciitis 48 0.031
896
DRY001 Dry Eye Syndrome 47 0.031
897
CLF056 Cleft Lip with or Without Cleft Palate 47 0.031
898
ACT055 Actinomycosis 47 0.031
899
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.031
900
RTN001 Retinal Vasculitis 47 0.031
901
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.031
902
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.031
903
c ACT076 Acute Myocarditis 46 0.031
904
HYP034 Hypertensive Encephalopathy 46 0.031
905
MDS022 Mediastinitis 46 0.031
906
PDT035 Pediatric Systemic Lupus Erythematosus 46 0.031
907
FLL008 Folliculitis 46 0.031
908
CHR008 Choroiditis 46 0.031
909
P MYC033 Myoclonus 46 0.031
910
c ACT042 Acute Pyelonephritis 46 0.031
911
P TRN034 Transverse Myelitis 45 0.031
912
ORL013 Oral Lichen Planus 45 0.031
913
HPT004 Hepatic Coma 45 0.031
914
CRB004 Cerebral Artery Occlusion 45 0.031
915
HYP059 Hypertelorism, Microtia, Facial Clefting Syndrome 45 0.031
916
CRD003 Cardiac Sarcoidosis 44 0.031
917
DYS018 Dysostosis 44 0.031
918
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.031
919
SBC012 Subcorneal Pustular Dermatosis 43 0.031
920
DVR002 Diverticulitis 43 0.031
921
P CLS010 Cluster Headache 42 0.031
922
DRG024 Drug Allergy 42 0.031
923
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.031
924
P HYP087 Hypotrichosis 42 0.031
925
LMB024 Limbic Encephalitis 41 0.031
926
LYM010 Lymph Node Tuberculosis 41 0.031
927
c FML015 Familial Nephrotic Syndrome 41 0.031
928
ULC007 Ulcerative Stomatitis 39 0.031
929
ERY017 Erythema Elevatum Diutinum 38 0.031
930
c ATM075 Autoimmune Encephalitis 38 0.031
931
ORF044 Orofacial Granulomatosis 38 0.031
932
NCR002 Necrobiosis Lipoidica 38 0.031
933
TRC005 Tracheal Stenosis 38 0.031
934
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.031
935
c ACQ042 Acquired Hemophilia a 37 0.031
936
RHM036 Rheumatoid Arthritis Interstitial Lung Disease 36 0.031
937
P ATM020 Autoimmune Enteropathy 35 0.031
938
c ATM022 Autoimmune Myocarditis 35 0.031
939
ATX010 Ataxia Neuropathy Spectrum 34 0.031
940
HNS001 Hansen's Disease 34 0.031
941
NNT011 Neonatal Anemia 34 0.031
942
ACT064 Acute Necrotizing Encephalitis 33 0.031
943
ORL022 Oral Erosive Lichen 33 0.031
944
KDN013 Kidney Hypertrophy 32 0.031
945
MLT035 Multifocal Choroiditis 32 0.031
946
PNC059 Punctate Inner Choroidopathy 32 0.031
947
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.031
948
CLN006 Colonic Pseudo-Obstruction 32 0.031
949
ACR017 Acrofacial Dysostosis 31 0.031
950
DFF031 Diffuse Alveolar Hemorrhage 30 0.031
951
GRN033 Granulomatous Mastitis 30 0.031
952
PCM002 Pauci-Immune Glomerulonephritis 30 0.031
953
c PST008 Posterior Scleritis 30 0.031
954
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 30 0.031
955
c ANT023 Anterior Scleritis 29 0.031
956
LST003 Listeria Meningitis 29 0.031
957
TBL025 Tubulointerstitial Nephritis with Uveitis 28 0.031
958
HYP018 Hyperglobulinemic Purpura 28 0.031
959
CTN019 Cutaneous Polyarteritis Nodosa 27 0.031
960
EXT059 External Auditory Canal, Bilateral Atresia of, with Congenital Vertical Talus 27 0.031
961
MDD015 Mid-Dermal Elastolysis 27 0.031
962
ACT162 Acute Sensory Ataxic Neuropathy 26 0.031
963
FBR028 Fibrosing Mediastinitis 26 0.031
964
MCR039 Macrophagic Myofasciitis 25 0.031
965
MCR093 Microtia-Anotia 25 0.031
966
UND004 Undetermined Colitis 24 0.031
967
c NPH105 Nephrotic Syndrome, Type 17 24 0.031
968
SVR055 Severe Immune-Mediated Enteropathy 24 0.031
969
c ANK021 Ankylosing Spondylitis 1 23 0.031
970
IDP095 Idiopathic Steroid-Resistant Nephrotic Syndrome 23 0.031
971
FDL001 Fiedler's Myocarditis 23 0.031
972
LNR005 Linear Scleroderma 22 0.031
973
P ACQ041 Acquired Amegakaryocytic Thrombocytopenia 21 0.031
974
c NPH107 Nephrotic Syndrome, Type 19 21 0.031
975
MTR027 Mitral Atresia 20 0.031
976
AND005 Androgen Insensitivity Syndrome, Mild 19 0.031
977
ORB010 Orbital Granuloma 19 0.031
978
RSM003 Rasmussen Subacute Encephalitis 19 0.031
979
EPS047 Epstein-Barr Virus-Associated Malignant Lymphoproliferative Disorder 18 0.031
980
HHV001 Hhv-6 Encephalitis 18 0.031
981
ANT063 Anti-P200 Pemphigoid 17 0.031
982
RSM002 Rasmussen Johnsen Thomsen Syndrome 17 0.031
983
BLD137 Blood Group--Ahonen 16 0.031
984
c PSD024 Pseudo Pelger-Huet Anomaly 14 0.031
985
ERY018 Erythema Nodosum, Idiopathic 10 0.031
986
IMM215 Immunodeficiency-Associated Lymphoproliferative Disease 8 0.031
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