Search results for Mycophenolic acid

1040 hits were found for Mycophenolic acid

# Family MCID Name MIFTS Score
1
c SYS001 Systemic Lupus Erythematosus 86 0.419
2
P KDN018 Kidney Disease 72 0.401
3
P GRF003 Graft-Versus-Host Disease 72 0.373
4
P LKM002 Leukemia 68 0.369
5
P LPS004 Lupus Erythematosus 61 0.367
6
P LVR013 Liver Disease 68 0.332
7
P DRR001 Diarrhea 55 0.327
8
P MYL006 Myeloid Leukemia 60 0.326
9
ATM095 Autoimmune Disease 62 0.318
10
P NTR004 Neutropenia 63 0.301
11
c LKM061 Leukemia, Acute Myeloid 84 0.296
12
P LYM118 Lymphoma 68 0.289
13
MYL009 Myelodysplastic Syndrome 70 0.281
14
DFC004 Deficiency Anemia 70 0.280
15
48X005 48,xyyy 39 0.271
16
END086 End Stage Renal Disease 51 0.269
17
LYM019 Lymphosarcoma 46 0.269
18
LVR012 Liver Cirrhosis 62 0.266
19
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.266
20
MYL069 Myeloma, Multiple 85 0.265
21
P GLM007 Glomerulonephritis 57 0.260
22
c ACT135 Acute Graft Versus Host Disease 52 0.258
23
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.257
24
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.255
25
CHL068 Cholestasis 61 0.248
26
P LKM062 Leukemia, Acute Lymphoblastic 69 0.246
27
HYP014 Hyperuricemia 52 0.245
28
P NRB001 Neuroblastoma 72 0.245
29
P NPH012 Nephrotic Syndrome 60 0.244
30
CLT003 Colitis 62 0.244
31
c CHR684 Chronic Kidney Disease 70 0.242
32
P PSR002 Psoriasis 62 0.240
33
PST011 Pustulosis of Palm and Sole 52 0.238
34
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.235
35
c LKM063 Leukemia, Chronic Myeloid 72 0.232
36
LNG099 Lung Disease 60 0.231
37
FTT001 Fatty Liver Disease 61 0.230
38
P BCL017 B-Cell Lymphoma 58 0.230
39
LPD008 Lipid Metabolism Disorder 62 0.230
40
P LKM071 Leukemia, Chronic Lymphocytic 79 0.226
41
DRM006 Dermatitis 61 0.226
42
ACT119 Acute Promyelocytic Leukemia 63 0.222
43
c HYP595 Hypertension, Essential 84 0.220
44
ADL002 Adult Syndrome 70 0.218
45
P SZR006 Seizure Disorder 56 0.218
46
HMT002 Hematologic Cancer 62 0.217
47
PLS009 Plasma Cell Neoplasm 51 0.216
48
VSL002 Visual Epilepsy 59 0.212
49
NRL016 Neural Tube Defects 82 0.211
50
c PRM038 Primary Agammaglobulinemia 44 0.211
51
P INF037 Inflammatory Bowel Disease 54 0.209
52
LYM133 Lymphoma, Hodgkin, Classic 69 0.208
53
CYT002 Cytokine Deficiency 42 0.208
54
P CLR023 Colorectal Cancer 99 0.206
55
ATH013 Atherosclerosis Susceptibility 65 0.206
56
c RHB024 Rhabdomyosarcoma 2 67 0.205
57
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.204
58
LYM040 Lymphoblastic Lymphoma 54 0.204
59
ISC004 Ischemia 58 0.204
60
c CHR064 Chronic Monocytic Leukemia 33 0.202
61
P VSC011 Vasculitis 62 0.200
62
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.198
63
MTB004 Metabolic Acidosis 50 0.198
64
P CNR004 Cone-Rod Dystrophy 2 73 0.197
65
HML018 Homologous Wasting Disease 22 0.196
66
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.195
67
HYP066 Hyperglycemia 61 0.195
68
P PRM006 Primary Biliary Cirrhosis 62 0.194
69
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.194
70
P DBT009 Diabetes Mellitus 64 0.194
71
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.193
72
P BRS047 Breast Cancer 97 0.191
73
c HYP836 Hypercholesterolemia, Familial, 1 73 0.190
74
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.189
75
c NRF023 Neurofibromatosis, Type Ii 80 0.188
76
P DRM053 Dermatitis, Atopic 66 0.187
77
P CRN300 Coronary Heart Disease 1 63 0.185
78
c ACT073 Acute Leukemia 58 0.185
79
P HYP750 Hypertriglyceridemia, Familial 62 0.184
80
HMN044 Human Immunodeficiency Virus Type 1 71 0.184
81
P DDN001 Duodenal Ulcer 52 0.184
82
PPT005 Peptic Ulcer Disease 59 0.183
83
SKN016 Skin Disease 63 0.182
84
CYT008 Cytomegalovirus Infection 57 0.181
85
NTR005 Nutritional Deficiency Disease 62 0.181
86
GST092 Gastroesophageal Reflux 67 0.181
87
c CHR417 Chronic Graft Versus Host Disease 57 0.180
88
P THR014 Thrombocytopenia 67 0.179
89
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.179
90
P HPT021 Hepatitis 67 0.179
91
P HPT023 Hepatocellular Carcinoma 100 0.179
92
GT001 Gout 64 0.176
93
c SCL052 Scleroderma, Familial Progressive 61 0.176
94
IGG001 Iga Glomerulonephritis 48 0.176
95
P TRN020 Turner Syndrome 67 0.176
96
ULC004 Ulcerative Colitis 73 0.176
97
HYP056 Hypoglycemia 66 0.174
98
P ENC018 Encephalopathy 61 0.173
99
c HPT073 Hepatitis C Virus 72 0.173
100
ALL026 Allergic Hypersensitivity Disease 62 0.172
101
CYS001 Cystic Fibrosis 81 0.172
102
P VSC007 Vascular Disease 63 0.172
103
CRH001 Crohn's Disease 74 0.172
104
MNT001 Mantle Cell Lymphoma 69 0.172
105
P PRS040 Prostate Cancer 97 0.172
106
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.172
107
ADR007 Adrenoleukodystrophy 75 0.171
108
BRK010 Burkitt Lymphoma 67 0.170
109
c ACT071 Acute Kidney Failure 60 0.169
110
P SRC025 Sarcoidosis 1 70 0.169
111
BNR002 Bone Resorption Disease 48 0.169
112
c MCR113 Microvascular Complications of Diabetes 3 52 0.166
113
P FLL037 Follicular Lymphoma 67 0.166
114
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.165
115
LPP008 Lipoprotein Quantitative Trait Locus 62 0.164
116
P SYS005 Systemic Scleroderma 68 0.164
117
IMM167 Immune Deficiency Disease 78 0.164
118
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.164
119
P GST044 Gastritis 56 0.164
120
c HPT001 Hepatitis C 62 0.163
121
P GLM045 Glioma 63 0.163
122
P OST002 Osteoporosis 74 0.162
123
P CHL066 Cholangitis 51 0.161
124
GLL048 Glial Tumor 45 0.161
125
P ESP024 Esophagitis 62 0.161
126
c FLL041 Follicular Lymphoma 1 49 0.160
127
PRT037 Pertussis 65 0.160
128
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.158
129
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.157
130
c MCR120 Microvascular Complications of Diabetes 7 47 0.157
131
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.157
132
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.157
133
c MCR130 Microvascular Complications of Diabetes 6 41 0.157
134
c MCR133 Microvascular Complications of Diabetes 4 41 0.157
135
P CRD246 Cardiovascular System Disease 57 0.156
136
INT066 Interstitial Lung Disease 60 0.156
137
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.155
138
P BND020 Bone Disease 59 0.154
139
P UVT001 Uveitis 57 0.154
140
P HRT032 Heart Disease 75 0.154
141
c ATM011 Autoimmune Hepatitis 63 0.154
142
MYL031 Myeloproliferative Neoplasm 66 0.153
143
c DBT099 Diabetes Mellitus, Type I 65 0.153
144
PRP030 Purpura 54 0.153
145
MCS002 Mucositis 56 0.151
146
P PNC035 Pancreatic Cancer 84 0.151
147
P CHR285 Chronic Myelomonocytic Leukemia 60 0.149
148
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.149
149
P MYS003 Myasthenia Gravis 68 0.148
150
P MYP004 Myopathy 70 0.148
151
c LKM005 Leukemia, T-Cell, Chronic 34 0.148
152
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.147
153
P PMP001 Pemphigus 54 0.147
154
c PRC016 Pre-Eclampsia 63 0.147
155
IRN002 Iron Metabolism Disease 57 0.147
156
P ART022 Arthritis 69 0.147
157
P NRP001 Neuropathy 56 0.147
158
BNM001 Bone Marrow Cancer 43 0.147
159
P MLT020 Multiple Sclerosis 72 0.147
160
ART140 Arteries, Anomalies of 52 0.145
161
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.144
162
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.143
163
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.143
164
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.143
165
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.143
166
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.143
167
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.143
168
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.143
169
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.143
170
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.143
171
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.143
172
P PNM007 Pneumonia 68 0.142
173
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.142
174
c ACT068 Acute Cystitis 63 0.142
175
P RHM011 Rheumatoid Arthritis 80 0.142
176
P PLM036 Pulmonary Fibrosis 65 0.142
177
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.141
178
PLS025 Plasmablastic Lymphoma 47 0.141
179
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.141
180
MCR004 Macroglobulinemia 49 0.140
181
BCT022 Bacterial Infectious Disease 56 0.140
182
DWN001 Down Syndrome 70 0.138
183
P ADN016 Adenocarcinoma 64 0.138
184
MRG003 Marginal Zone B-Cell Lymphoma 52 0.138
185
47X002 47,xyy 49 0.138
186
P MYC007 Myocardial Infarction 70 0.136
187
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.136
188
P EXN002 Exanthem 57 0.135
189
P MMB011 Membranous Nephropathy 50 0.134
190
P HRP006 Herpes Simplex 65 0.134
191
CRB039 Cerebrovascular Disease 67 0.134
192
P ART021 Arteriosclerosis 54 0.134
193
MYL005 Myelofibrosis 70 0.133
194
P ALP008 Alopecia 54 0.133
195
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.133
196
HRW001 Hair Whorl 36 0.133
197
ATX019 Ataxia with Vitamin E Deficiency 42 0.133
198
STR067 Stroke, Ischemic 81 0.133
199
OST159 Osteogenic Sarcoma 66 0.133
200
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.132
201
c SYS043 Systemic Lupus Erythematosus 1 38 0.132
202
OCL069 Ocular Motor Apraxia 51 0.131
203
WLD007 Waldenstroem's Macroglobulinemia 61 0.131
204
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.131
205
P SKN015 Skin Carcinoma 66 0.131
206
URM002 Uremia 49 0.130
207
THR024 Thrombosis 57 0.130
208
RFR010 Refractory Anemia 48 0.130
209
P CYS018 Cystitis 59 0.130
210
c HPT016 Hepatitis B 59 0.130
211
HPT004 Hepatic Coma 45 0.129
212
MYC006 Mycosis Fungoides 66 0.129
213
STT001 Status Epilepticus 60 0.129
214
LYM012 Lymphoplasmacytic Lymphoma 47 0.129
215
CNS004 Constipation 58 0.129
216
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.128
217
P RSP003 Respiratory Failure 74 0.128
218
BLL006 Bullous Pemphigoid 62 0.127
219
FNG017 Fungal Infectious Disease 53 0.127
220
CHL079 Children's Interstitial Lung Disease 26 0.126
221
P TRM003 Tremor 54 0.126
222
DPR016 Depression 63 0.125
223
RNL077 Renal Fibrosis 47 0.125
224
SQM006 Squamous Cell Carcinoma 60 0.125
225
P ENC004 Encephalitis 61 0.125
226
P CTR002 Cataract 60 0.125
227
P BLD134 Bladder Cancer 79 0.125
228
CHL014 Cholera 59 0.124
229
P ADL017 Adult T-Cell Leukemia 56 0.123
230
P LYM033 Lymphoproliferative Syndrome 59 0.123
231
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.123
232
GST023 Gastric Ulcer 53 0.123
233
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.123
234
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.123
235
HDG004 Hodgkin's Granuloma 23 0.122
236
HDG006 Hodgkin's Paragranuloma 22 0.122
237
CNN005 Connective Tissue Disease 68 0.122
238
c ACT027 Acute Pancreatitis 60 0.122
239
CRV035 Cervical Cancer 76 0.122
240
PMP006 Pemphigus Vulgaris, Familial 57 0.121
241
P GST053 Gastric Cancer 83 0.120
242
DFF005 Diffuse Large B-Cell Lymphoma 55 0.120
243
HRY003 Hairy Cell Leukemia 55 0.120
244
P CTN015 Cutaneous T Cell Lymphoma 49 0.119
245
STM007 Stomatitis 50 0.119
246
P SCL009 Sclerosing Cholangitis 48 0.119
247
P FCL005 Focal Segmental Glomerulosclerosis 57 0.118
248
SZR001 Sezary's Disease 60 0.118
249
EYD002 Eye Disease 58 0.118
250
P MNN013 Meningitis 66 0.118
251
P PNC044 Pancreatitis 61 0.118
252
INS024 Insulin-Like Growth Factor I 79 0.118
253
ADR022 Adrenomyeloneuropathy 38 0.117
254
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.117
255
c INH020 Inherited Metabolic Disorder 47 0.117
256
P LTR001 Lateral Sclerosis 54 0.116
257
MNT002 Mental Depression 58 0.116
258
SVR004 Severe Combined Immunodeficiency 73 0.116
259
c HPT003 Hepatitis a 62 0.116
260
P HML002 Hemolytic Anemia 63 0.115
261
GLC003 Glucose Intolerance 54 0.115
262
CNG034 Congestive Heart Failure 69 0.115
263
P DRM010 Dermatomyositis 61 0.114
264
P MLN008 Melanoma 69 0.114
265
c FML035 Familial Hyperlipidemia 55 0.113
266
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.112
267
OST003 Osteonecrosis 61 0.112
268
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.112
269
c DRR009 Diarrhea 6 46 0.112
270
HRP004 Herpes Zoster 60 0.112
271
ACQ007 Acquired Immunodeficiency Syndrome 60 0.112
272
ALL014 Allergic Encephalomyelitis 38 0.111
273
HYP005 Hypokalemia 55 0.111
274
P AMY004 Amyloidosis 70 0.111
275
c THR092 Thrombophilia Due to Thrombin Defect 73 0.111
276
CLN015 Colon Adenocarcinoma 65 0.111
277
P THL005 Thalassemia 60 0.110
278
P SCK005 Sickle Cell Disease 50 0.110
279
CHC001 Chickenpox 60 0.110
280
PLM033 Pulmonary Embolism 59 0.110
281
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.110
282
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.110
283
P MCR115 Microvascular Complications of Diabetes 5 66 0.110
284
SRC014 Sarcoma 65 0.110
285
SPN035 Spindle Cell Sarcoma 53 0.110
286
P PLY019 Polyneuropathy 56 0.109
287
BRR014 Barrett Esophagus 65 0.109
288
c CHL119 Cholangitis, Primary Sclerosing 57 0.109
289
GLM044 Glomerular Disease 37 0.109
290
RCK004 Rickets 68 0.108
291
c FNC043 Fanconi Anemia, Complementation Group E 62 0.108
292
PPL022 Papilloma 54 0.108
293
CLF027 Cleft Palate, Isolated 64 0.108
294
PRT036 Peritonitis 64 0.108
295
SPN186 Spinal Cord Injury 60 0.108
296
RTC005 Reticulosarcoma 47 0.108
297
IDP091 Idiopathic Nephrotic Syndrome 42 0.107
298
BRN002 Bronchiolitis 59 0.107
299
VRL011 Viral Infectious Disease 61 0.107
300
ATM052 Autoimmune Disease 1 37 0.107
301
P INF032 Infertility 57 0.107
302
P KDN017 Kidney Cancer 60 0.106
303
c ACT134 Acute Liver Failure 56 0.106
304
P APL001 Aplastic Anemia 74 0.106
306
P PRP019 Peripheral Nervous System Disease 58 0.106
307
VCC001 Vaccinia 49 0.105
308
P HYP098 Hypereosinophilic Syndrome 67 0.105
309
SQM002 Squamous Cell Papilloma 46 0.105
310
P INF038 Influenza 68 0.105
311
P OVR082 Overgrowth Syndrome 50 0.104
312
KRT009 Keratosis 51 0.103
313
c CHR418 Chronic Leukemia 49 0.103
314
LYM051 Lymphomatoid Granulomatosis 45 0.103
315
CRB004 Cerebral Artery Occlusion 45 0.103
316
P ANP001 Anaplastic Large Cell Lymphoma 58 0.103
317
ENT011 Enterocolitis 51 0.102
318
DFF003 Diffuse Scleroderma 41 0.102
319
SPL004 Splenic Marginal Zone Lymphoma 51 0.102
320
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.102
321
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.102
322
LYS012 Lysosomal Acid Lipase Deficiency 65 0.101
323
PRX001 Peroxisomal Disease 46 0.101
324
c SVR001 Severe Acute Respiratory Syndrome 62 0.101
325
PRL017 Prolymphocytic Leukemia 47 0.100
326
BRN024 Bronchitis 68 0.100
327
c DWL002 Dowling-Degos Disease 1 58 0.100
328
P AST007 Astrocytoma 51 0.099
329
c VRL010 Viral Hepatitis 52 0.099
330
P PLY018 Polycythemia 56 0.099
331
PLM010 Pulmonary Edema 54 0.099
332
TXC005 Toxic Shock Syndrome 62 0.099
333
SCK003 Sickle Cell Anemia 74 0.099
334
LYM027 Lymphopenia 58 0.099
336
ERY051 Erythroleukemia, Familial 56 0.098
337
ANC002 Anca-Associated Vasculitis 41 0.098
338
AGN016 Aging 56 0.097
339
BRN012 Bronchiolitis Obliterans 55 0.097
340
ATY042 Atypical Chronic Myeloid Leukemia 49 0.097
341
P SPP010 Suppressor of Tumorigenicity 3 51 0.097
342
ENT004 Enthesopathy 49 0.097
343
CNT047 Contact Dermatitis 58 0.096
344
P TMP001 Temporal Lobe Epilepsy 50 0.096
345
BLR008 Bilirubin Metabolic Disorder 57 0.096
346
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.096
347
P URT039 Urticaria 58 0.096
348
PRP036 Peripheral T-Cell Lymphoma 53 0.095
349
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.095
350
P FBR017 Fibrosarcoma 56 0.095
351
P RTN024 Retinoblastoma 73 0.095
352
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.095
353
c FML008 Familial Retinoblastoma 53 0.095
354
P PRL003 Proliferative Glomerulonephritis 44 0.095
355
HYP081 Hypolipoproteinemia 51 0.094
356
GST050 Gastrointestinal System Disease 56 0.094
357
P MSC005 Muscular Dystrophy 66 0.094
358
MDD011 Mood Disorder 62 0.094
359
AVN001 Avian Influenza 59 0.094
360
P HDC001 Headache 57 0.093
361
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.093
362
P PYL005 Pyelonephritis 56 0.093
363
CHL149 Childhood Acute Myeloid Leukemia 44 0.093
364
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.092
365
P MYC084 Mycobacterium Tuberculosis 1 68 0.092
366
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.092
367
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.092
368
CLF001 Cleft Lip 53 0.092
369
KPS004 Kaposi Sarcoma 75 0.091
370
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.091
371
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.091
372
PRT013 Portal Hypertension 59 0.090
373
P PLY041 Polymyositis 57 0.090
374
PNC001 Pancytopenia 54 0.089
375
PYD002 Pyoderma 50 0.089
376
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.089
377
PLY001 Polycythemia Vera 69 0.089
378
ATS010 Autosomal Recessive Disease 48 0.088
379
P MYS005 Myositis 56 0.088
380
P HYP069 Hyperparathyroidism 63 0.088
381
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.088
382
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.088
383
P RNL015 Renal Hypertension 47 0.088
384
RTN023 Retinitis 46 0.088
385
NRR001 Neuroretinitis 42 0.088
386
TTN003 Tetanus 65 0.087
387
P IGN003 Iga Nephropathy 1 49 0.087
388
DYS073 Dysphagia 50 0.087
389
P ECL001 Eclampsia 50 0.087
390
P MYC008 Myocarditis 59 0.086
391
PST046 Post-Transplant Lymphoproliferative Disease 53 0.086
392
HNS001 Hansen's Disease 34 0.086
393
P LPR021 Leprosy 3 69 0.086
394
PRP027 Peripheral Vascular Disease 71 0.086
395
NRM001 Neuromyelitis Optica 61 0.085
396
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.085
397
P FNC004 Fanconi Syndrome 50 0.085
398
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.085
399
c PSR017 Psoriasis 2 53 0.085
400
c PSR023 Psoriasis 1 52 0.085
401
c PSR032 Psoriasis 11 47 0.085
402
c PSR028 Psoriasis 7 42 0.085
403
c PSR018 Psoriasis 13 41 0.085
404
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.084
405
MSC007 Muscle Hypertrophy 64 0.084
406
P INT143 Interstitial Cystitis 61 0.084
407
P DNG005 Dengue Virus 59 0.084
408
P LNG064 Lung Cancer Susceptibility 3 78 0.083
409
PLS011 Plasmacytoma 56 0.083
410
P PLM037 Pulmonary Hypertension 67 0.082
411
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.082
412
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.082
413
P LCH002 Lichen Planus 53 0.082
414
P PLY014 Polycystic Kidney Disease 62 0.081
415
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.081
416
ACT058 Active Peptic Ulcer Disease 55 0.081
417
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.081
418
URT010 Ureteral Obstruction 45 0.081
419
c INF145 Infantile Liver Failure Syndrome 1 50 0.081
420
c BTT014 Beta-Thalassemia 74 0.081
421
PLS016 Plasma Cell Leukemia 53 0.081
422
P FNC034 Fanconi Renotubular Syndrome 2 40 0.081
423
AMN001 Amenorrhea 54 0.081
424
P ART023 Arthropathy 62 0.080
425
HMG005 Hemoglobinopathy 56 0.080
426
c MCR129 Microvascular Complications of Diabetes 1 66 0.080
427
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.080
428
P EPD016 Epidermolysis Bullosa 53 0.080
429
THR004 Thrombocytosis 51 0.080
430
MSL001 Measles 62 0.079
431
P ESS003 Essential Thrombocythemia 68 0.079
432
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.079
433
BLR001 Biliary Atresia 50 0.079
434
MMB001 Membranoproliferative Glomerulonephritis 55 0.079
436
c LCL006 Localized Scleroderma 62 0.079
437
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.078
438
ALL010 Allergic Contact Dermatitis 56 0.078
439
ACT003 Acute Kidney Tubular Necrosis 45 0.078
440
c PRM012 Primary Polycythemia 50 0.078
441
DMY004 Demyelinating Disease 52 0.078
442
SPR126 Superior Semicircular Canal Dehiscence 40 0.078
443
c HMG029 Hemoglobin Se Disease 39 0.078
444
MST005 Mastitis 53 0.078
445
CVD001 Covid-19 44 0.077
446
MCR088 Microscopic Polyangiitis 51 0.077
447
GRN037 Granulomatosis with Polyangiitis 65 0.077
448
GLS018 Glass Syndrome 57 0.077
449
IDP011 Idiopathic Interstitial Pneumonia 59 0.077
450
INT054 Intraocular Lymphoma 48 0.077
451
KRT006 Keratoconjunctivitis 53 0.077
452
CRH005 Crohn's Colitis 53 0.077
453
c ATR087 Atrial Standstill 1 75 0.077
454
P MNC007 Monocytic Leukemia 53 0.076
455
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.076
456
PYD001 Pyoderma Gangrenosum 54 0.076
457
P RTN016 Retinal Degeneration 53 0.076
458
c ALP101 Alpha-Thalassemia 62 0.076
459
LYS002 Lysosomal Storage Disease 52 0.076
460
P ALP009 Alopecia Areata 60 0.076
461
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.075
462
LRG008 Large Granular Lymphocyte Leukemia 41 0.075
463
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.075
464
ORL015 Oral Squamous Cell Carcinoma 43 0.075
465
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.075
466
c DLT002 Dilated Cardiomyopathy 79 0.074
467
CYT004 Cytomegalic Inclusion Disease 31 0.074
468
c SPN225 Spondyloarthropathy 1 73 0.074
469
P CND004 Candidiasis 58 0.074
470
NRM005 Neuromuscular Disease 64 0.074
471
P PRK057 Parkinson Disease, Late-Onset 78 0.073
472
P RHB003 Rhabdomyosarcoma 63 0.073
473
HMS001 Hemosiderosis 54 0.073
474
c THR090 Thrombocythemia 1 49 0.073
475
PNC129 Pancreatic Adenocarcinoma 68 0.073
476
SKN019 Skin Melanoma 68 0.073
477
P HML001 Hemolytic-Uremic Syndrome 53 0.073
478
INT067 Interstitial Nephritis 48 0.073
479
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.073
480
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.072
481
CHR286 Chronic Neutrophilic Leukemia 42 0.072
482
KRT001 Keratoconjunctivitis Sicca 49 0.072
483
FRY002 Fryns Syndrome 43 0.072
484
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.072
485
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.071
486
P RRH023 Rare Hereditary Hemochromatosis 41 0.071
487
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.071
488
OVR094 Ovarian Epithelial Cancer 38 0.071
489
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.071
490
MDD018 Middle East Respiratory Syndrome 43 0.071
491
P NRV007 Nervous System Disease 66 0.071
492
P OPT006 Optic Nerve Disease 60 0.070
493
TRN015 Transient Cerebral Ischemia 63 0.070
494
P FML011 Familial Adenomatous Polyposis 72 0.070
495
P HMP007 Hemophilia 51 0.070
496
CHR073 Choreatic Disease 52 0.070
497
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.070
498
MCR103 Microtia 43 0.070
499
FDL002 Food Allergy 51 0.069
500
HYD002 Hydronephrosis 60 0.069
501
c HYP272 Hypercholesterolemia, Familial, 3 44 0.069
502
MXD050 Mixed Phenotype Acute Leukemia 43 0.069
503
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.069
504
SPL018 Splenomegaly 48 0.069
505
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.069
506
P CLC063 Celiac Disease 1 66 0.069
507
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.069
508
CLF004 Cleft Lip/palate 54 0.068
509
CLS052 Classic Hairy Cell Leukemia 27 0.068
510
SFT003 Soft Tissue Sarcoma 56 0.068
511
c ALM001 Al Amyloidosis 50 0.068
512
DSS009 Disseminated Intravascular Coagulation 57 0.068
513
GRN017 Granulocytopenia 44 0.068
514
P SHR001 Short Bowel Syndrome 53 0.068
515
c CHR682 Chronic Bilirubin Encephalopathy 39 0.067
516
IMM136 Immune System Disease 45 0.067
517
49X006 49, Xxxxy Syndrome 41 0.067
518
c MCR112 Microvascular Complications of Diabetes 2 41 0.067
519
P SJG008 Sjogren Syndrome 61 0.067
520
c ANM038 Anemia, Autoimmune Hemolytic 62 0.067
521
P DYS154 Dystonia 65 0.067
522
c INF071 Inflammatory Bowel Disease 1 67 0.066
523
P LKD001 Leukodystrophy 59 0.066
524
c INT064 Intermediate Uveitis 55 0.066
525
PNM001 Pneumocystosis 59 0.066
526
P CRN037 Craniosynostosis 68 0.066
527
GST040 Gastric Adenocarcinoma 70 0.065
528
P BRN022 Bronchiectasis 59 0.065
529
PSR001 Psoriatic Arthritis 61 0.065
530
SPN051 Spondylitis 51 0.065
531
INF009 Inflammatory Spondylopathy 31 0.065
532
CHR563 Chronic Eosinophilic Leukemia 48 0.065
533
ILS001 Ileus 51 0.064
534
HMG002 Hemoglobinuria 50 0.064
535
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.064
536
FCT007 Factor Vii Deficiency 67 0.064
537
P SCL015 Scleritis 48 0.064
538
MYL020 Myelomeningocele 51 0.064
539
MCR013 Microphthalmia 57 0.064
540
PLG002 Plague 63 0.064
541
MCL006 Macular Retinal Edema 55 0.064
542
P PNV001 Panuveitis 50 0.064
543
MSC157 Muscular Dystrophy, Duchenne Type 72 0.063
544
TRN018 Transitional Cell Carcinoma 56 0.063
545
P CTN003 Cutaneous Lupus Erythematosus 53 0.063
546
LTH001 Lethal Midline Granuloma 44 0.063
547
ANR007 Anorexia Nervosa 63 0.063
548
TXC002 Toxic Encephalopathy 53 0.063
549
ERY003 Erythema Multiforme 58 0.063
550
P ANT006 Antiphospholipid Syndrome 55 0.063
551
ALC006 Alcoholic Hepatitis 61 0.062
552
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.062
553
c LKM070 Leukemia, Acute Monocytic 57 0.062
554
P MYC033 Myoclonus 46 0.062
555
LKP003 Leukoplakia 39 0.062
556
OCL020 Ocular Cicatricial Pemphigoid 55 0.062
557
WST005 West Nile Virus 54 0.062
558
CLR109 Colorectal Adenocarcinoma 51 0.062
559
P ASP006 Aspergillosis 69 0.062
560
P THY023 Thymoma 65 0.062
561
c THY107 Thymoma, Familial 52 0.062
562
P MTR014 Motor Neuron Disease 65 0.062
563
MST004 Mast Cell Neoplasm 42 0.062
564
EXT007 Extracutaneous Mastocytoma 38 0.062
565
SCH036 Scheie Syndrome 72 0.062
566
RDC006 Red Cell Aplasia 43 0.062
567
RTN017 Retinal Detachment 61 0.061
568
WTH001 Withdrawal Disorder 48 0.061
569
JPN002 Japanese Encephalitis 57 0.061
570
INC002 Inclusion Body Myositis 58 0.061
571
c CNT035 Central Nervous System Disease 52 0.061
572
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.061
573
c FNC027 Fanconi Anemia, Complementation Group a 81 0.060
574
INT002 Intermittent Claudication 61 0.060
575
P THY032 Thyroiditis 52 0.060
576
P MLG074 Malignant Mesenchymoma 40 0.060
577
RTR011 Retroperitoneal Fibrosis 40 0.060
578
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.060
579
DRY001 Dry Eye Syndrome 47 0.059
580
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.059
581
PLR008 Pleurisy 50 0.059
582
ACR041 Acromelic Frontonasal Dysostosis 52 0.059
583
HMR023 Hemorrhagic Cystitis 45 0.059
584
CCT002 Cicatricial Pemphigoid 51 0.059
585
P CHR012 Chronic Granulomatous Disease 67 0.059
586
HPT022 Hepatoblastoma 56 0.059
587
HST010 Histiocytosis 48 0.058
588
MNN009 Meningoencephalitis 49 0.058
589
KRT019 Keratitis, Hereditary 65 0.058
590
c NPH049 Nephrotic Syndrome, Type 2 48 0.058
591
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.058
592
P TXP001 Toxoplasmosis 60 0.058
593
HPT014 Hepatorenal Syndrome 50 0.058
594
MGK001 Megakaryocytic Leukemia 64 0.058
595
DDN006 Duodenitis 49 0.057
596
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.057
597
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.057
598
URN010 Urinary Tract Obstruction 55 0.057
599
P MMP001 Mumps 58 0.057
600
BCK006 Back Pain 42 0.057
601
GST037 Gastroparesis 54 0.057
602
CRC021 Carcinosarcoma 62 0.057
603
c BCT007 Bacterial Meningitis 55 0.056
604
DGR001 Digeorge Syndrome 64 0.056
605
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.056
606
P GRV001 Graves' Disease 55 0.056
607
RDN001 Reading Disorder 40 0.056
608
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.055
609
c JVN010 Juvenile Rheumatoid Arthritis 64 0.055
610
P MST002 Mast-Cell Leukemia 49 0.055
611
P PRR002 Pure Red-Cell Aplasia 47 0.055
612
RFR002 Refractory Hairy Cell Leukemia 33 0.055
613
c DPH024 Diaphragmatic Hernia, Congenital 63 0.055
614
P GNG009 Gangliosidosis 44 0.055
615
c WLM018 Wilms Tumor 5 61 0.055
616
CRD223 Cardiac Arrhythmia 60 0.055
617
c PST005 Posterior Uveitis 54 0.055
618
YLL002 Yellow Fever 61 0.054
619
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.054
620
ANR004 Anuria 46 0.054
621
P AGM001 Agammaglobulinemia 65 0.054
622
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.054
623
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.054
624
SDD001 Sudden Infant Death Syndrome 61 0.053
625
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.053
626
c SCN007 Secondary Hyperparathyroidism 51 0.053
627
BRN014 Bronchopneumonia 54 0.053
628
c ACT004 Acute Diarrhea 39 0.053
629
ACT200 Acute Monoblastic Leukemia 52 0.053
630
GNG012 Gingival Overgrowth 51 0.053
631
c ATM099 Autoimmune Uveitis 45 0.053
632
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.053
633
CHR001 Churg-Strauss Syndrome 61 0.053
634
CYS036 Cystinosis, Nephropathic 51 0.053
635
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 0.053
636
P MCL001 Mucolipidosis 48 0.053
637
TRP009 Triple X Syndrome 42 0.053
638
c ACT042 Acute Pyelonephritis 46 0.053
639
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.053
640
ACN002 Acanthosis Nigricans 60 0.052
641
ILT001 Ileitis 50 0.052
642
P MST009 Mastocytosis 64 0.052
643
KRT008 Keratopathy 47 0.052
644
EXT034 Extrinsic Allergic Alveolitis 58 0.052
645
P CNT005 Central Nervous System Lymphoma 53 0.052
646
LPD004 Lipoid Nephrosis 46 0.052
647
c GM1007 Gm1 Gangliosidosis 62 0.052
648
ORL012 Oral Leukoplakia 39 0.052
649
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.052
650
c BKV001 Bk-Virus Nephropathy 24 0.052
651
P ANG015 Angioedema 57 0.052
652
PNN001 Panniculitis 51 0.051
653
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.051
654
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.051
655
PLM012 Pulmonary Sarcoidosis 53 0.051
656
P DMY001 Demyelinating Polyneuropathy 43 0.051
657
IRD001 Iridocyclitis 53 0.051
658
ACT088 Acute Insulin Response 41 0.051
659
CLB010 Coloboma of Macula 52 0.051
660
P TRC086 Trichohepatoenteric Syndrome 1 62 0.051
661
P MCR010 Microcephaly 59 0.051
662
c HYP768 Hyperlipoproteinemia, Type I 67 0.051
663
HYP063 Hypersplenism 53 0.050
664
ESP020 Esophageal Atresia 62 0.050
665
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.050
666
ACT029 Acute Interstitial Pneumonia 49 0.050
667
SYS071 Systemic Autoimmune Disease 37 0.050
668
THR123 Thrombotic Microangiopathy 36 0.050
669
SPT004 Septic Arthritis 58 0.050
670
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.050
671
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.050
672
P KRB001 Krabbe Disease 69 0.050
673
GRM010 Germ Cells Tumors 34 0.050
674
LST001 Listeriosis 56 0.050
675
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.050
676
c PRM226 Primary Central Nervous System Lymphoma 48 0.050
677
IDP033 Idiopathic Edema 44 0.050
678
CMR002 Coumarin Resistance 56 0.050
679
LYM005 Lymphocele 35 0.050
680
TKY002 Takayasu Arteritis 62 0.050
681
EWN003 Ewing Sarcoma 69 0.049
682
CLR030 Clear Cell Renal Cell Carcinoma 53 0.049
683
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.049
684
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.049
685
ASP007 Aspiration Pneumonia 48 0.049
686
AYM001 Ayme-Gripp Syndrome 57 0.049
687
ALS001 Alstrom Syndrome 64 0.049
688
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.049
689
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.049
690
EPD006 Epidermolysis Bullosa Acquisita 49 0.049
691
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.049
692
FBR089 Fibrosclerosis, Multifocal 38 0.049
693
P INT070 Intestinal Obstruction 58 0.049
694
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.049
695
LMB024 Limbic Encephalitis 41 0.049
696
FSC004 Fasciitis 50 0.049
697
P PLY020 Polyradiculoneuropathy 48 0.049
698
CRS001 Crescentic Glomerulonephritis 43 0.049
699
P WSK001 Wiskott-Aldrich Syndrome 72 0.048
700
P DMN001 Diamond-Blackfan Anemia 69 0.048
701
ACT098 Acute Erythroid Leukemia 48 0.048
702
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.048
703
HRP008 Herpes Simiae 25 0.048
704
TND005 Tendinitis 54 0.048
705
BCT004 Bacteriuria 49 0.048
706
SVR097 Severe Cutaneous Adverse Reaction 69 0.048
707
HNC001 Henoch-Schoenlein Purpura 55 0.048
708
P MTC003 Metachromatic Leukodystrophy 70 0.048
709
MYL001 Myelitis 51 0.048
710
GST010 Gestational Trophoblastic Neoplasm 46 0.048
711
LNG108 Langerhans Cell Histiocytosis 58 0.048
712
c HMP029 Hemophilia a 67 0.047
713
HRT011 Heart Septal Defect 50 0.047
714
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.047
715
c JVN061 Juvenile Arthritis 60 0.047
716
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.047
717
CRT013 Carotid Stenosis 50 0.047
718
ERY066 Erythema Multiforme Major 30 0.047
719
P PRM002 Primary Hyperoxaluria 62 0.047
720
HRL003 Hurler Syndrome 65 0.047
721
HPT046 Hepatic Veno-Occlusive Disease 56 0.047
722
HYP748 Hypertelorism 50 0.047
723
P OCL013 Oculodentodigital Dysplasia 69 0.047
724
SKN013 Skin Benign Neoplasm 51 0.047
725
CYT018 Cytochrome P450 2d6 Variant 27 0.047
726
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.047
727
P PLY017 Polyarteritis Nodosa 58 0.047
728
CMB003 Combined T Cell and B Cell Immunodeficiency 49 0.047
729
ALL012 Allergic Angiitis 24 0.047
730
MRF001 Marfan Syndrome 77 0.046
731
CMM004 Common Variable Immunodeficiency 68 0.046
732
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.046
733
THR013 Thoracic Outlet Syndrome 54 0.046
734
P HMR003 Hemorrhagic Disease 53 0.046
735
P TYS001 Tay-Sachs Disease 69 0.046
736
c HPT007 Hepatitis E 53 0.046
737
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.046
738
P PLY188 Polyendocrinopathy 32 0.046
739
c DNG003 Dengue Disease 59 0.046
740
BRS051 Breast Disease 58 0.046
741
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.046
742
MLG164 Malignant Epithelial Tumor of Ovary 26 0.046
743
P HYP024 Hypoparathyroidism 56 0.046
744
RYN005 Raynaud Phenomenon 47 0.046
745
P ANR048 Aniridia 1 63 0.045
746
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 68 0.045
747
CMB081 Combined Immunodeficiency, X-Linked 36 0.045
749
PRT058 Pure Autonomic Failure 59 0.045
750
ANL018 Analbuminemia 54 0.045
751
THR035 Thrombasthenia 40 0.045
752
FXD003 Fixed Drug Eruption 35 0.045
753
P GLL022 Guillain-Barre Syndrome 59 0.045
754
VLC001 Velocardiofacial Syndrome 54 0.045
755
VGN017 Vaginal Cancer 60 0.045
756
P URF003 Urofacial Syndrome 1 57 0.045
757
URN009 Urinary System Disease 48 0.045
758
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.045
759
WLS001 Wilson Disease 71 0.044
760
PRC013 Pericarditis 54 0.044
761
MCP033 Mucopolysaccharidoses 38 0.044
762
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.044
763
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.044
764
c ATM075 Autoimmune Encephalitis 38 0.044
765
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.044
766
c ADL093 Adult Acute Monocytic Leukemia 20 0.044
767
SKN022 Skin Squamous Cell Carcinoma 57 0.044
768
EXP004 Exophthalmos 52 0.044
770
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.044
771
PLY043 Polyomavirus Allograft Nephropathy 13 0.044
772
INT303 Intracranial Hypertension, Idiopathic 57 0.044
773
P DBT005 Diabetes Insipidus 55 0.044
774
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.044
775
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.044
776
c SRC023 Sarcoidosis 2 43 0.043
777
P OVR096 Overlap Myositis 27 0.043
778
MST024 Mastocytosis, Cutaneous 69 0.043
779
ABD010 Abdominal Wall Defect 36 0.043
780
ATX010 Ataxia Neuropathy Spectrum 34 0.043
781
ACT064 Acute Necrotizing Encephalitis 33 0.043
782
BLD137 Blood Group--Ahonen 16 0.043
783
P PRC012 Pericardial Effusion 51 0.043
784
HMP001 Hemopericardium 48 0.043
785
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.043
786
SPH010 Sphingolipidosis 47 0.043
787
CRN020 Coronary Restenosis 39 0.043
788
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.042
789
ADN001 Adenosine Deaminase Deficiency 47 0.042
790
PLY023 Polycystic Liver Disease 57 0.042
791
BBS001 Babesiosis 48 0.042
792
P DYS007 Dyskeratosis Congenita 67 0.042
793
P HYP077 Hypertrichosis 50 0.042
794
c CHL140 Chilblain Lupus 1 58 0.042
795
CRT016 Carotid Artery Disease 52 0.042
796
CRD043 Ceroid Storage Disease 44 0.042
797
ASP002 Aspartylglucosaminuria 62 0.041
798
CLF056 Cleft Lip with or Without Cleft Palate 47 0.041
799
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.041
800
P TST021 Testicular Germ Cell Tumor 60 0.041
801
HMP005 Hemiplegia 55 0.041
802
CRD137 Cardiogenic Shock 47 0.041
803
ORL013 Oral Lichen Planus 45 0.041
804
CLC006 Calcinosis 48 0.041
805
P PRT026 Parotitis 42 0.041
806
CHR463 Chronic Actinic Dermatitis 37 0.040
807
RNL011 Renal Osteodystrophy 50 0.040
808
c INV001 Invasive Aspergillosis 49 0.040
809
c BCT013 Bacterial Pneumonia 48 0.040
810
CHD001 Chediak-Higashi Syndrome 66 0.040
811
ENT001 Enterocele 39 0.040
812
TTH004 Tethered Spinal Cord Syndrome 35 0.040
813
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 0.040
814
TRP005 Trophoblastic Neoplasm 38 0.040
815
PLY179 Polyomavirus-Associated Nephropathy 24 0.040
816
CNN003 Conn's Syndrome 79 0.040
817
HSH003 Hashimoto Thyroiditis 62 0.040
818
FLL008 Folliculitis 46 0.040
819
DVR002 Diverticulitis 43 0.040
820
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.039
821
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.039
822
CLL014 Cll/sll 45 0.039
823
PGM030 Pigmentation Anomaly of the Skin 26 0.039
824
CMP010 Complex Regional Pain Syndrome 58 0.039
825
P STR020 Strabismus 55 0.039
826
MCH006 Mechanical Strabismus 42 0.039
827
ADL030 Adult-Onset Still's Disease 58 0.039
828
CHL028 Childhood Type Dermatomyositis 58 0.039
829
FML285 Familial Apolipoprotein C-Ii Deficiency 29 0.039
830
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 19 0.039
831
c DMN023 Diamond-Blackfan Anemia 1 53 0.039
832
FML026 Familial Lipoprotein Lipase Deficiency 51 0.039
833
EXT010 Extramedullary Plasmacytoma 45 0.039
834
P TST026 Testicular Germ Cell Cancer 43 0.039
835
CDQ001 Cauda Equina Syndrome 38 0.039
836
c ATM045 Autoimmune Glomerulonephritis 36 0.039
837
BLD053 Blood Platelet Disease 49 0.038
838
P BLD051 Blood Coagulation Disease 46 0.038
839
MYC088 Mycobacterium Avium Complex Infections 29 0.038
840
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.037
841
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.037
842
GLM004 Gliomatosis Cerebri 52 0.037
843
MYL003 Myeloid Sarcoma 49 0.037
844
PGM001 Pigmented Villonodular Synovitis 56 0.037
845
c PST041 Posterior Urethral Valves 41 0.037
846
c HRD202 Hereditary Lymphedema I 50 0.037
847
GLN010 Glanzmann Thrombasthenia 66 0.037
848
HYD038 Hydrops Fetalis, Nonimmune 62 0.037
849
P ATR010 Atrial Heart Septal Defect 60 0.037
850
MLL001 Molluscum Contagiosum 50 0.037
851
c DRM054 Dermatitis, Atopic, 2 44 0.037
852
SND001 Sandhoff Disease 68 0.037
853
c MNN047 Mannosidosis, Alpha B, Lysosomal 66 0.037
854
c ATM024 Autoimmune Pancreatitis 55 0.037
855
DSC009 Discoid Lupus Erythematosus 42 0.037
856
P PST059 Pustular Psoriasis 37 0.037
857
EVN001 Evans' Syndrome 48 0.037
858
ANT039 Antisynthetase Syndrome 46 0.037
859
MLT075 Multifocal Motor Neuropathy 46 0.037
860
NDL003 Nodular Nonsuppurative Panniculitis 39 0.037
861
PFF001 Pfeiffer Syndrome 79 0.036
862
P TTR001 Tetralogy of Fallot 70 0.036
863
AND014 Androgenic Alopecia 46 0.036
864
DRG024 Drug Allergy 42 0.036
865
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.036
866
P CRB059 Cerebellar Degeneration 37 0.036
867
DYS164 Dyskeratosis Congenita, X-Linked 60 0.036
868
PRN038 Prune Belly Syndrome 56 0.036
869
PTT041 Pituitary Stalk Interruption Syndrome 50 0.036
870
RFR013 Refractory Celiac Disease 35 0.036
871
LTT002 Letterer-Siwe Disease 33 0.036
872
c TST046 Testicular Germ Cell Tumor 1 29 0.036
873
P SHW006 Shwachman-Diamond Syndrome 1 67 0.036
874
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.036
875
FCS002 Fucosidosis 61 0.036
876
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.036
877
OBS082 Obstructive Nephropathy 42 0.036
878
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.036
879
LNG039 Lung Squamous Cell Carcinoma 66 0.035
880
NCR007 Necrotizing Fasciitis 48 0.035
881
PRL008 Paralytic Ileus 45 0.035
882
c PRM108 Primary Progressive Multiple Sclerosis 51 0.035
883
MLR002 Miliary Tuberculosis 49 0.035
884
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.035
885
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 0.035
886
INT051 Intussusception 53 0.035
887
CYT005 Cytomegalovirus Retinitis 50 0.035
888
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.034
889
VGT001 Vogt-Koyanagi-Harada Disease 55 0.034
890
P PLG001 Pelger-Huet Anomaly 51 0.034
891
c ACQ014 Acquired Hemophilia 45 0.034
892
ISC015 Ischemic Colitis 44 0.034
893
PLY021 Polyradiculopathy 41 0.034
894
LNR006 Linear Iga Disease 40 0.034
895
P BCL005 B Cell Prolymphocytic Leukemia 39 0.034
896
RFR004 Refractory Hematologic Cancer 30 0.034
897
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.034
898
AGM019 Agammaglobulinemia, X-Linked 71 0.034
899
MDS022 Mediastinitis 46 0.034
900
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.034
901
c MCP001 Mucopolysaccharidosis Iii 65 0.034
902
PRS012 Pars Planitis 48 0.034
903
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.033
904
DBL002 Double Outlet Right Ventricle 56 0.033
905
SCH038 Schopf-Schulz-Passarge Syndrome 55 0.033
906
ASH001 Asherman's Syndrome 31 0.033
907
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.033
908
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.033
909
P OCY003 Oocyte Maturation Defect 1 45 0.033
910
P CLS010 Cluster Headache 42 0.033
911
TRC005 Tracheal Stenosis 38 0.033
912
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.032
913
MCR141 Mucormycosis 56 0.032
914
HRL004 Hurler-Scheie Syndrome 55 0.032
915
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.032
916
c PSR021 Psoriasis 14, Pustular 50 0.032
917
CRY004 Cryoglobulinemia 48 0.032
918
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.032
919
ATY022 Atypical Coarctation of Aorta 34 0.032
920
MRD002 Marden-Walker Syndrome 56 0.032
921
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 51 0.032
922
GNT019 Giant Cell Myocarditis 30 0.032
924
FRY006 Fryns Microphthalmia Syndrome 52 0.032
925
PPL021 Papilledema 49 0.032
926
ACT055 Actinomycosis 47 0.032
927
CWP001 Cowpox 46 0.032
928
DYS018 Dysostosis 44 0.032
929
DRG002 Drug-Induced Hepatitis 43 0.032
930
DFF031 Diffuse Alveolar Hemorrhage 30 0.032
931
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.031
932
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 48 0.031
933
MGS001 Megaesophagus 43 0.031
934
HDG001 Hodgkin's Lymphoma, Nodular Sclerosis 37 0.031
935
HDG005 Hodgkin's Lymphoma, Mixed Cellularity 30 0.031
936
c SYS066 Systemic Polyarteritis Nodosa 26 0.031
937
HMP028 Hemophagocytic Syndrome Associated with an Infection 24 0.031
938
NPH010 Nephrosclerosis 50 0.031
939
ULC007 Ulcerative Stomatitis 39 0.031
940
c HYP794 Hyperoxaluria, Primary, Type I 63 0.030
941
MXD005 Mixed Connective Tissue Disease 58 0.030
942
PTT009 Pituitary Gland Disease 54 0.030
943
P PLM006 Pulmonary Alveolar Proteinosis 53 0.030
944
BLL003 Bell's Palsy 51 0.030
945
c PYR010 Peyronie's Disease 50 0.030
946
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.030
947
ACT162 Acute Sensory Ataxic Neuropathy 26 0.030
948
FTL073 Fetal Anticonvulsant Syndrome 26 0.030
949
GDP001 Goodpasture Syndrome 55 0.029
950
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.029
951
BRD025 Birdshot Chorioretinopathy 48 0.029
952
TCL003 T Cell Deficiency 46 0.029
953
CRB001 Cerebral Lymphoma 39 0.029
954
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.029
955
CHR208 Chromosome 17p Deletion 23 0.029
956
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.029
957
CPR004 Coproporphyria, Hereditary 57 0.029
958
NCR004 Nocardiosis 54 0.029
959
ERD001 Erdheim-Chester Disease 53 0.029
960
ACT017 Acute Chest Syndrome 51 0.029
961
PRT018 Portal Vein Thrombosis 50 0.029
962
TNS014 Tenosynovitis 44 0.029
963
P HYP087 Hypotrichosis 42 0.029
964
NCR002 Necrobiosis Lipoidica 38 0.029
965
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.029
966
AND005 Androgen Insensitivity Syndrome, Mild 19 0.029
967
LYM010 Lymph Node Tuberculosis 41 0.028
968
ADH001 Adhesions of Uterus 36 0.028
969
RVS001 Revesz Syndrome 54 0.027
970
HYR002 Hoyeraal Hreidarsson Syndrome 46 0.027
971
CNT046 Central Nervous System Vasculitis 44 0.027
972
c MYL058 Myeloproliferative Syndrome, Transient 44 0.027
973
KMR001 Kimura Disease 43 0.027
974
ERM002 Ear Malformation 39 0.027
975
P INH011 Inherited Bone Marrow Failure Syndromes 34 0.027
976
P PLM069 Pulmonary Venous Return Anomaly 26 0.027
977
P ALP004 Alport Syndrome 68 0.027
978
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.027
979
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.027
980
CHR078 Chorioretinitis 50 0.027
981
RTN001 Retinal Vasculitis 47 0.027
982
CRD003 Cardiac Sarcoidosis 44 0.027
983
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.027
984
c ATM022 Autoimmune Myocarditis 35 0.027
985
CHR103 Charge Syndrome 67 0.026
986
RBR001 Roberts Syndrome 64 0.026
987
RLP001 Relapsing Polychondritis 54 0.026
988
HYP074 Hypersensitivity Vasculitis 51 0.026
989
SCT005 Scott Syndrome 49 0.026
990
RHM036 Rheumatoid Arthritis Interstitial Lung Disease 36 0.026
991
P ECT006 Ectodermal Dysplasia 62 0.025
992
MCS006 Macs Syndrome 58 0.025
993
c LSS005 Lissencephaly 1 56 0.025
994
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 51 0.025
995
INT071 Intestinal Perforation 51 0.025
996
CRY014 Cryptococcal Meningitis 48 0.025
997
HPT009 Hepatopulmonary Syndrome 48 0.025
998
ESN015 Eosinophilic Fasciitis 48 0.025
999
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.025
1000
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.025
1001
CHR008 Choroiditis 46 0.025
1002
CRV043 Cervical Dystonia 42 0.025
1003
PRN032 Paraneoplastic Cerebellar Degeneration 28 0.025
1004
c INF152 Infectious Posterior Uveitis 19 0.025
1005
c NNN032 Non-Infectious Posterior Uveitis 19 0.025
1006
c INF151 Infectious Panuveitis 14 0.025
1007
PMS001 Poems Syndrome 60 0.023
1008
STR008 Strongyloidiasis 51 0.023
1009
PST062 Pustulosis Palmaris Et Plantaris 47 0.023
1010
c ACT076 Acute Myocarditis 46 0.023
1011
P TRN034 Transverse Myelitis 45 0.023
1012
c FML015 Familial Nephrotic Syndrome 41 0.023
1013
MNK002 Monkeypox 39 0.023
1014
KDN013 Kidney Hypertrophy 32 0.023
1015
CLN006 Colonic Pseudo-Obstruction 32 0.023
1016
c ANK021 Ankylosing Spondylitis 1 23 0.023
1017
LNR005 Linear Scleroderma 22 0.023
1018
CMP062 Complication After Organ Transplantation 13 0.023
1019
FBR086 Fibrolamellar Carcinoma 61 0.021
1020
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 58 0.021
1021
PLM070 Pulmonic Stenosis 57 0.021
1022
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 57 0.021
1023
HYP034 Hypertensive Encephalopathy 46 0.021
1024
IMM078 Immunodeficiency 21 42 0.021
1025
ORF044 Orofacial Granulomatosis 38 0.021
1026
LYM052 Lymphomatoid Papulosis 38 0.021
1027
GNG006 Gingival Hypertrophy 34 0.021
1028
NNT011 Neonatal Anemia 34 0.021
1029
MLT035 Multifocal Choroiditis 32 0.021
1030
ACR017 Acrofacial Dysostosis 31 0.021
1031
c PST008 Posterior Scleritis 30 0.021
1032
c NPH096 Nephrotic Syndrome, Type 12 29 0.021
1033
TBL025 Tubulointerstitial Nephritis with Uveitis 28 0.021
1034
MCR093 Microtia-Anotia 25 0.021
1035
c NPH073 Nephrotic Syndrome, Type 8 25 0.021
1036
BRT037 Brittle Diabetes 25 0.021
1037
FDL001 Fiedler's Myocarditis 23 0.021
1038
ANT063 Anti-P200 Pemphigoid 17 0.021
1039
TCL006 T Cell Immunodeficiency Primary 11 0.021
1040
RFR001 Refractory Plasma Cell Neoplasm 10 0.021
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