Search results for Azathioprine

783 hits were found for Azathioprine

# Family MCID Name MIFTS Score
1
CRH001 Crohn's Disease 74 0.517
2
P INF037 Inflammatory Bowel Disease 54 0.432
3
ULC004 Ulcerative Colitis 73 0.350
4
P NTR004 Neutropenia 63 0.297
5
c SYS001 Systemic Lupus Erythematosus 86 0.296
6
CLT003 Colitis 62 0.288
7
P LPS004 Lupus Erythematosus 61 0.247
8
ALL026 Allergic Hypersensitivity Disease 62 0.236
9
CRH005 Crohn's Colitis 53 0.234
10
P VSC011 Vasculitis 62 0.233
11
ATM095 Autoimmune Disease 62 0.211
12
c INF071 Inflammatory Bowel Disease 1 67 0.205
13
c ATM011 Autoimmune Hepatitis 63 0.203
14
P MYS003 Myasthenia Gravis 68 0.200
15
DRM006 Dermatitis 61 0.198
16
P GLM007 Glomerulonephritis 57 0.195
17
P RHM011 Rheumatoid Arthritis 80 0.187
18
PNC001 Pancytopenia 54 0.181
19
P PNC044 Pancreatitis 61 0.176
20
P MLT020 Multiple Sclerosis 72 0.164
21
c ACT027 Acute Pancreatitis 60 0.164
22
P PMP001 Pemphigus 54 0.156
23
P LVR013 Liver Disease 68 0.150
24
ANC002 Anca-Associated Vasculitis 41 0.150
25
P LYM118 Lymphoma 68 0.148
26
P ART022 Arthritis 69 0.144
27
P HPT021 Hepatitis 67 0.142
28
P EXN002 Exanthem 57 0.140
29
P DRM053 Dermatitis, Atopic 66 0.138
30
c PRM038 Primary Agammaglobulinemia 44 0.136
31
P PSR002 Psoriasis 62 0.134
32
BLL006 Bullous Pemphigoid 62 0.134
33
PST011 Pustulosis of Palm and Sole 52 0.134
34
P THR014 Thrombocytopenia 67 0.129
35
LNG099 Lung Disease 60 0.129
36
P KDN018 Kidney Disease 72 0.127
37
P NPH012 Nephrotic Syndrome 60 0.127
38
P DRR001 Diarrhea 55 0.127
39
PRP030 Purpura 54 0.127
40
LVR012 Liver Cirrhosis 62 0.124
41
THP001 Thiopurine S Methyltranferase Deficiency 20 0.124
42
GRN037 Granulomatosis with Polyangiitis 65 0.122
43
CHL068 Cholestasis 61 0.122
44
PRT013 Portal Hypertension 59 0.122
45
NRM001 Neuromyelitis Optica 61 0.119
46
PMP006 Pemphigus Vulgaris, Familial 57 0.119
47
MCR088 Microscopic Polyangiitis 51 0.119
48
P SKN015 Skin Carcinoma 66 0.117
49
P ALP008 Alopecia 54 0.117
50
END086 End Stage Renal Disease 51 0.117
51
CYT008 Cytomegalovirus Infection 57 0.114
52
NDL013 Nodular Regenerative Hyperplasia 47 0.114
53
c SYS043 Systemic Lupus Erythematosus 1 38 0.114
54
P PLM036 Pulmonary Fibrosis 65 0.112
55
INT066 Interstitial Lung Disease 60 0.109
56
P THP004 Thiopurines, Poor Metabolism of, 1 47 0.106
57
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.103
58
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.103
59
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.101
60
P DRM010 Dermatomyositis 61 0.098
61
LYM027 Lymphopenia 58 0.098
62
P UVT001 Uveitis 57 0.098
63
P PLY041 Polymyositis 57 0.098
64
HPT046 Hepatic Veno-Occlusive Disease 56 0.098
65
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.094
66
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.094
67
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.094
68
RDC006 Red Cell Aplasia 43 0.094
69
48X005 48,xyyy 39 0.094
70
ATM052 Autoimmune Disease 1 37 0.094
71
DFC004 Deficiency Anemia 70 0.091
72
CNN005 Connective Tissue Disease 68 0.091
73
c SCL052 Scleroderma, Familial Progressive 61 0.091
74
CNT047 Contact Dermatitis 58 0.091
75
IGG001 Iga Glomerulonephritis 48 0.091
76
P PRM006 Primary Biliary Cirrhosis 62 0.088
77
P PRR002 Pure Red-Cell Aplasia 47 0.088
78
c CHR684 Chronic Kidney Disease 70 0.084
79
P THY023 Thymoma 65 0.084
80
SKN016 Skin Disease 63 0.084
81
c HPT003 Hepatitis a 62 0.084
82
P MYL006 Myeloid Leukemia 60 0.084
83
c THY107 Thymoma, Familial 52 0.084
84
P MMB011 Membranous Nephropathy 50 0.084
85
P PRL003 Proliferative Glomerulonephritis 44 0.084
86
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.081
87
P MYP004 Myopathy 70 0.081
88
P HML002 Hemolytic Anemia 63 0.081
89
P PLY017 Polyarteritis Nodosa 58 0.081
90
ATX019 Ataxia with Vitamin E Deficiency 42 0.081
91
NTR042 Neutrophilic Dermatosis, Acute Febrile 38 0.081
92
P SRC025 Sarcoidosis 1 70 0.077
93
NTR005 Nutritional Deficiency Disease 62 0.077
94
HRP004 Herpes Zoster 60 0.077
95
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.077
96
CHC001 Chickenpox 60 0.077
97
c VRL010 Viral Hepatitis 52 0.077
99
P CHL066 Cholangitis 51 0.077
100
P LKM002 Leukemia 68 0.073
101
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.073
102
GT001 Gout 64 0.073
103
CHR001 Churg-Strauss Syndrome 61 0.073
104
P ENC018 Encephalopathy 61 0.073
105
IDP011 Idiopathic Interstitial Pneumonia 59 0.073
106
P LYM033 Lymphoproliferative Syndrome 59 0.073
107
BRN002 Bronchiolitis 59 0.073
108
BCT022 Bacterial Infectious Disease 56 0.073
109
BRN012 Bronchiolitis Obliterans 55 0.073
110
CHR463 Chronic Actinic Dermatitis 37 0.073
111
ALL012 Allergic Angiitis 24 0.073
112
P HPT023 Hepatocellular Carcinoma 100 0.069
113
AST005 Asthma 76 0.069
114
MYL009 Myelodysplastic Syndrome 70 0.069
115
LYM133 Lymphoma, Hodgkin, Classic 69 0.069
116
P HYP098 Hypereosinophilic Syndrome 67 0.069
117
c JVN010 Juvenile Rheumatoid Arthritis 64 0.069
118
P PLY019 Polyneuropathy 56 0.069
119
c ATM024 Autoimmune Pancreatitis 55 0.069
120
c PSR017 Psoriasis 2 53 0.069
121
c PSR023 Psoriasis 1 52 0.069
122
ENT004 Enthesopathy 49 0.069
123
ACT029 Acute Interstitial Pneumonia 49 0.069
124
P SCL009 Sclerosing Cholangitis 48 0.069
125
c PSR032 Psoriasis 11 47 0.069
126
GRN017 Granulocytopenia 44 0.069
127
c PSR028 Psoriasis 7 42 0.069
128
c PSR018 Psoriasis 13 41 0.069
129
c LKM061 Leukemia, Acute Myeloid 84 0.065
130
P GRF003 Graft-Versus-Host Disease 72 0.065
131
P AMY004 Amyloidosis 70 0.065
132
P LPR021 Leprosy 3 69 0.065
133
P PNM007 Pneumonia 68 0.065
134
P VSC007 Vascular Disease 63 0.065
135
P ALP009 Alopecia Areata 60 0.065
136
P BCL017 B-Cell Lymphoma 58 0.065
137
P URT039 Urticaria 58 0.065
138
P MYS005 Myositis 56 0.065
139
PYD001 Pyoderma Gangrenosum 54 0.065
140
AMN001 Amenorrhea 54 0.065
141
PYD002 Pyoderma 50 0.065
142
c DRR009 Diarrhea 6 46 0.065
143
GLM044 Glomerular Disease 37 0.065
144
HNS001 Hansen's Disease 34 0.065
145
UND004 Undetermined Colitis 24 0.065
146
ADL002 Adult Syndrome 70 0.060
147
P SYS005 Systemic Scleroderma 68 0.060
148
P HRP006 Herpes Simplex 65 0.060
149
c ANM038 Anemia, Autoimmune Hemolytic 62 0.060
150
P MYC008 Myocarditis 59 0.060
151
GST045 Gastroenteritis 59 0.060
152
ERY003 Erythema Multiforme 58 0.060
153
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.060
154
EXT034 Extrinsic Allergic Alveolitis 58 0.060
155
c CHL119 Cholangitis, Primary Sclerosing 57 0.060
156
P INT068 Intestinal Disease 53 0.060
157
HYP014 Hyperuricemia 52 0.060
158
P PNV001 Panuveitis 50 0.060
159
SPL018 Splenomegaly 48 0.060
160
P CLL015 Collagen Disease 47 0.060
161
RTN001 Retinal Vasculitis 47 0.060
162
ACT003 Acute Kidney Tubular Necrosis 45 0.060
163
ILC002 Ileocolitis 43 0.060
164
RFR013 Refractory Celiac Disease 35 0.060
165
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.055
166
c BSL007 Basal Cell Carcinoma 68 0.055
167
c DBT099 Diabetes Mellitus, Type I 65 0.055
168
SQM006 Squamous Cell Carcinoma 60 0.055
169
VRC005 Varicose Veins 60 0.055
170
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.055
171
c HPT016 Hepatitis B 59 0.055
172
P OPT009 Optic Neuritis 57 0.055
173
c CHR417 Chronic Graft Versus Host Disease 57 0.055
174
P HDC001 Headache 57 0.055
175
P FCL005 Focal Segmental Glomerulosclerosis 57 0.055
176
P ANG015 Angioedema 57 0.055
177
HMS001 Hemosiderosis 54 0.055
178
P LCH002 Lichen Planus 53 0.055
179
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.055
180
IRD001 Iridocyclitis 53 0.055
181
DMY004 Demyelinating Disease 52 0.055
182
NRT004 Neuritis 52 0.055
183
MYL001 Myelitis 51 0.055
184
P IGN003 Iga Nephropathy 1 49 0.055
185
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 48 0.055
186
ANT039 Antisynthetase Syndrome 46 0.055
187
RTC009 Reticulum Cell Sarcoma 43 0.055
188
PMP004 Pemphigus Foliaceus 43 0.055
189
CYT002 Cytokine Deficiency 42 0.055
190
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.055
191
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.055
192
PLS002 Peliosis Hepatis 33 0.055
193
LYM043 Lymphocytic Hypophysitis 32 0.055
194
PDT027 Pediatric Ulcerative Colitis 28 0.055
195
c SYS066 Systemic Polyarteritis Nodosa 26 0.055
196
c HYP595 Hypertension, Essential 84 0.049
197
PFF001 Pfeiffer Syndrome 79 0.049
198
IMM167 Immune Deficiency Disease 78 0.049
199
KPS004 Kaposi Sarcoma 75 0.049
200
c ATR087 Atrial Standstill 1 75 0.049
201
P OST002 Osteoporosis 74 0.049
202
c SPN225 Spondyloarthropathy 1 73 0.049
203
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.049
204
CNG034 Congestive Heart Failure 69 0.049
205
CMM004 Common Variable Immunodeficiency 68 0.049
206
P TRN020 Turner Syndrome 67 0.049
207
c RHB024 Rhabdomyosarcoma 2 67 0.049
208
ALC007 Alcohol Dependence 66 0.049
209
P MNN013 Meningitis 66 0.049
210
TTN003 Tetanus 65 0.049
211
SRC014 Sarcoma 65 0.049
212
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.049
213
c JVN061 Juvenile Arthritis 60 0.049
214
INC002 Inclusion Body Myositis 58 0.049
215
c ACT134 Acute Liver Failure 56 0.049
216
P NRP001 Neuropathy 56 0.049
217
HNC001 Henoch-Schoenlein Purpura 55 0.049
218
SYN007 Synovitis 54 0.049
219
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.049
220
c PST005 Posterior Uveitis 54 0.049
221
P TRM003 Tremor 54 0.049
222
PLM012 Pulmonary Sarcoidosis 53 0.049
223
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.049
224
P CNT005 Central Nervous System Lymphoma 53 0.049
225
SPN035 Spindle Cell Sarcoma 53 0.049
226
SPN051 Spondylitis 51 0.049
227
SKN013 Skin Benign Neoplasm 51 0.049
228
ILT001 Ileitis 50 0.049
229
47X002 47,xyy 49 0.049
230
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.049
231
P SCL015 Scleritis 48 0.049
232
c PRM226 Primary Central Nervous System Lymphoma 48 0.049
233
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.049
234
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.049
235
LYM019 Lymphosarcoma 46 0.049
236
P TRN034 Transverse Myelitis 45 0.049
237
HPT004 Hepatic Coma 45 0.049
238
LYM051 Lymphomatoid Granulomatosis 45 0.049
239
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.049
240
P PLM085 Pulmonary Hemosiderosis 44 0.049
241
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.049
242
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.049
243
C1N001 C1 Inhibitor Deficiency 39 0.049
244
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.049
245
PLC002 Plica Syndrome 36 0.049
246
INF009 Inflammatory Spondylopathy 31 0.049
247
HMR013 Hemorrhagic Proctocolitis 17 0.049
248
c NRF023 Neurofibromatosis, Type Ii 80 0.042
249
P HRT032 Heart Disease 75 0.042
250
P APL001 Aplastic Anemia 74 0.042
251
P RSP003 Respiratory Failure 74 0.042
252
SCK003 Sickle Cell Anemia 74 0.042
253
c HYP836 Hypercholesterolemia, Familial, 1 73 0.042
254
BHC003 Behcet Syndrome 71 0.042
255
DWN001 Down Syndrome 70 0.042
256
SVR097 Severe Cutaneous Adverse Reaction 69 0.042
257
P TMP003 Temporal Arteritis 68 0.042
258
P CLC063 Celiac Disease 1 66 0.042
259
P ATR011 Atrial Fibrillation 66 0.042
260
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.042
261
NRM005 Neuromuscular Disease 64 0.042
262
c PRC016 Pre-Eclampsia 63 0.042
263
DPR016 Depression 63 0.042
264
c HPT001 Hepatitis C 62 0.042
265
P ESP024 Esophagitis 62 0.042
266
P ART023 Arthropathy 62 0.042
267
MDD011 Mood Disorder 62 0.042
268
TXC005 Toxic Shock Syndrome 62 0.042
269
P ENC004 Encephalitis 61 0.042
270
P TXP001 Toxoplasmosis 60 0.042
271
HPT019 Hepatic Encephalopathy 60 0.042
272
P SNS001 Sensorineural Hearing Loss 60 0.042
273
ADN018 Adenoma 59 0.042
274
c ACT073 Acute Leukemia 58 0.042
275
EYD002 Eye Disease 58 0.042
276
P PTY003 Pityriasis Rubra Pilaris 58 0.042
277
CHL067 Cholecystitis 57 0.042
278
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.042
279
P CRD246 Cardiovascular System Disease 57 0.042
280
CMR002 Coumarin Resistance 56 0.042
281
HMT008 Hematuria, Benign Familial 56 0.042
282
P GST044 Gastritis 56 0.042
283
HST011 Histoplasmosis 55 0.042
284
VGT001 Vogt-Koyanagi-Harada Disease 55 0.042
285
c BCT007 Bacterial Meningitis 55 0.042
286
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.042
287
PRC013 Pericarditis 54 0.042
288
PST046 Post-Transplant Lymphoproliferative Disease 53 0.042
289
P HYP083 Hypopituitarism 53 0.042
290
c GLL024 Gallbladder Disease 1 53 0.042
291
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.042
292
P HMP007 Hemophilia 51 0.042
293
THR004 Thrombocytosis 51 0.042
294
OCL069 Ocular Motor Apraxia 51 0.042
295
MGL001 Megaloblastic Anemia 51 0.042
296
P SCK005 Sickle Cell Disease 50 0.042
297
HDR003 Hidradenitis 49 0.042
298
MNN009 Meningoencephalitis 49 0.042
299
URM002 Uremia 49 0.042
300
INT067 Interstitial Nephritis 48 0.042
301
PRS012 Pars Planitis 48 0.042
303
CRD137 Cardiogenic Shock 47 0.042
304
P PLL002 Pellagra 46 0.042
305
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.042
306
OLG001 Oligospermia 45 0.042
307
c ACQ014 Acquired Hemophilia 45 0.042
308
c ATM099 Autoimmune Uveitis 45 0.042
309
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.042
310
SPR126 Superior Semicircular Canal Dehiscence 40 0.042
311
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.042
312
c HMG029 Hemoglobin Se Disease 39 0.042
313
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.042
314
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.042
315
ERY066 Erythema Multiforme Major 30 0.042
316
P OVR096 Overlap Myositis 27 0.042
317
CHL079 Children's Interstitial Lung Disease 26 0.042
318
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.042
319
PRM331 Primary Hypophysitis 18 0.042
320
CNN003 Conn's Syndrome 79 0.034
321
c MNN043 Meningioma, Familial 74 0.034
322
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.034
323
c THR092 Thrombophilia Due to Thrombin Defect 73 0.034
324
P FML018 Familial Mediterranean Fever 73 0.034
325
ANX010 Anxiety 73 0.034
326
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.034
327
MSC157 Muscular Dystrophy, Duchenne Type 72 0.034
328
SCH036 Scheie Syndrome 72 0.034
329
c HPT073 Hepatitis C Virus 72 0.034
330
P ASP006 Aspergillosis 69 0.034
331
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.034
332
CHL065 Cholangiocarcinoma 68 0.034
333
c HMP029 Hemophilia a 67 0.034
334
P PRP003 Porphyria Cutanea Tarda 67 0.034
335
P MSC005 Muscular Dystrophy 66 0.034
336
P NRV007 Nervous System Disease 66 0.034
337
KRT019 Keratitis, Hereditary 65 0.034
338
PRT037 Pertussis 65 0.034
339
HRL003 Hurler Syndrome 65 0.034
340
ATH013 Atherosclerosis Susceptibility 65 0.034
341
PRT036 Peritonitis 64 0.034
342
BRC012 Brucellosis 64 0.034
343
MSC007 Muscle Hypertrophy 64 0.034
344
P ADN016 Adenocarcinoma 64 0.034
345
c ACT068 Acute Cystitis 63 0.034
346
c LCL006 Localized Scleroderma 62 0.034
347
LPP008 Lipoprotein Quantitative Trait Locus 62 0.034
348
LSC001 Lesch-Nyhan Syndrome 62 0.034
349
MNN042 Meningioma, Radiation-Induced 62 0.034
350
P PRP029 Porphyria 62 0.034
351
PSR001 Psoriatic Arthritis 61 0.034
352
RTN017 Retinal Detachment 61 0.034
353
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.034
354
P GLY013 Glycogen Storage Disease 60 0.034
355
P OPT006 Optic Nerve Disease 60 0.034
356
CHL014 Cholera 59 0.034
357
P BRN022 Bronchiectasis 59 0.034
358
P CYS018 Cystitis 59 0.034
359
P GLL022 Guillain-Barre Syndrome 59 0.034
360
CRY005 Cryptococcosis 58 0.034
361
P INT070 Intestinal Obstruction 58 0.034
362
ADL030 Adult-Onset Still's Disease 58 0.034
363
MNT002 Mental Depression 58 0.034
364
P CND004 Candidiasis 58 0.034
365
MXD005 Mixed Connective Tissue Disease 58 0.034
366
GLS018 Glass Syndrome 57 0.034
367
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 57 0.034
368
P PYL005 Pyelonephritis 56 0.034
369
P FBR017 Fibrosarcoma 56 0.034
370
ERY051 Erythroleukemia, Familial 56 0.034
371
ALL010 Allergic Contact Dermatitis 56 0.034
372
GST050 Gastrointestinal System Disease 56 0.034
373
MCR141 Mucormycosis 56 0.034
374
MCS002 Mucositis 56 0.034
375
DFF005 Diffuse Large B-Cell Lymphoma 55 0.034
376
P ANT006 Antiphospholipid Syndrome 55 0.034
377
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.034
378
OCL020 Ocular Cicatricial Pemphigoid 55 0.034
379
HRL004 Hurler-Scheie Syndrome 55 0.034
380
c INT064 Intermediate Uveitis 55 0.034
381
P DBT005 Diabetes Insipidus 55 0.034
382
CRY001 Cryptogenic Organizing Pneumonia 53 0.034
383
HYP063 Hypersplenism 53 0.034
384
c MCR113 Microvascular Complications of Diabetes 3 52 0.034
385
c ACT135 Acute Graft Versus Host Disease 52 0.034
386
FCT001 Factor Viii Deficiency 51 0.034
387
INT079 Intrahepatic Cholangiocarcinoma 51 0.034
388
ESP002 Esophageal Varix 51 0.034
389
P PRC012 Pericardial Effusion 51 0.034
390
GNG012 Gingival Overgrowth 51 0.034
391
CCT002 Cicatricial Pemphigoid 51 0.034
392
PNN001 Panniculitis 51 0.034
393
HYP074 Hypersensitivity Vasculitis 51 0.034
394
P HYP077 Hypertrichosis 50 0.034
395
SPN021 Spinal Meningioma 50 0.034
396
P ECL001 Eclampsia 50 0.034
397
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.034
398
LPR001 Lepromatous Leprosy 50 0.034
399
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.034
400
SLD003 Sialadenitis 49 0.034
401
VCC001 Vaccinia 49 0.034
402
CGN006 Cogan Syndrome 48 0.034
403
RFR010 Refractory Anemia 48 0.034
404
ACT098 Acute Erythroid Leukemia 48 0.034
405
HMP001 Hemopericardium 48 0.034
406
P PLY020 Polyradiculoneuropathy 48 0.034
407
SYM002 Sympathetic Ophthalmia 47 0.034
408
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.034
409
P INN002 Inner Ear Disease 47 0.034
410
c MCR120 Microvascular Complications of Diabetes 7 47 0.034
411
RYN005 Raynaud Phenomenon 47 0.034
412
MCR191 Microscopic Colitis 46 0.034
413
FLL008 Folliculitis 46 0.034
414
ELS001 Eales Disease 45 0.034
415
URT010 Ureteral Obstruction 45 0.034
416
HMR023 Hemorrhagic Cystitis 45 0.034
417
MCR017 Macrocytic Anemia 44 0.034
418
CRS001 Crescentic Glomerulonephritis 43 0.034
419
NSP002 Nasopharyngitis 43 0.034
420
c SRC023 Sarcoidosis 2 43 0.034
421
P DMY001 Demyelinating Polyneuropathy 43 0.034
422
c RTN047 Retinitis Pigmentosa 18 42 0.034
423
IDP091 Idiopathic Nephrotic Syndrome 42 0.034
424
NRR001 Neuroretinitis 42 0.034
425
P PHT010 Photoparoxysmal Response 1 42 0.034
426
MNN002 Mononeuritis Multiplex 41 0.034
427
c MCR130 Microvascular Complications of Diabetes 6 41 0.034
428
c MCR133 Microvascular Complications of Diabetes 4 41 0.034
429
DFF003 Diffuse Scleroderma 41 0.034
430
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.034
431
SCR001 Secretory Meningioma 41 0.034
432
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.034
433
RTR011 Retroperitoneal Fibrosis 40 0.034
434
PCH007 Pouchitis 39 0.034
435
OCL025 Ocular Toxoplasmosis 39 0.034
436
MLT016 Multicentric Reticulohistiocytosis 39 0.034
437
P XNT004 Xanthinuria 39 0.034
438
MCP033 Mucopolysaccharidoses 38 0.034
439
FBR089 Fibrosclerosis, Multifocal 38 0.034
440
PMP010 Pompholyx 37 0.034
441
RHM014 Rheumatoid Vasculitis 37 0.034
442
SYS071 Systemic Autoimmune Disease 37 0.034
443
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.034
444
ACL001 Acalculous Cholecystitis 35 0.034
446
c FML324 Familial Porphyria Cutanea Tarda 31 0.034
447
c HRD142 Hereditary Xanthinuria 31 0.034
448
LST003 Listeria Meningitis 29 0.034
449
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.034
450
HML018 Homologous Wasting Disease 22 0.034
451
P CLR023 Colorectal Cancer 99 0.024
452
P LNG032 Lung Cancer 98 0.024
453
P BRS047 Breast Cancer 97 0.024
454
P OVR042 Ovarian Cancer 88 0.024
455
MYL069 Myeloma, Multiple 85 0.024
456
MLR004 Malaria 81 0.024
457
CYS001 Cystic Fibrosis 81 0.024
458
STR067 Stroke, Ischemic 81 0.024
459
P LNG064 Lung Cancer Susceptibility 3 78 0.024
460
P PRK057 Parkinson Disease, Late-Onset 78 0.024
461
CRV035 Cervical Cancer 76 0.024
462
ADR007 Adrenoleukodystrophy 75 0.024
463
END057 Endometrial Cancer 74 0.024
464
c HMC039 Hemochromatosis, Type 1 74 0.024
465
SVR004 Severe Combined Immunodeficiency 73 0.024
466
P CNR004 Cone-Rod Dystrophy 2 73 0.024
467
OTT002 Otitis Media 72 0.024
468
PRP027 Peripheral Vascular Disease 71 0.024
469
P MYC007 Myocardial Infarction 70 0.024
470
MYL005 Myelofibrosis 70 0.024
471
P OCL013 Oculodentodigital Dysplasia 69 0.024
472
P HYP086 Hypothyroidism 69 0.024
473
ART016 Aortic Aneurysm 69 0.024
474
P LKM062 Leukemia, Acute Lymphoblastic 69 0.024
475
P INF038 Influenza 68 0.024
476
RCK004 Rickets 68 0.024
477
P CRD119 Cardiac Arrest 67 0.024
478
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.024
479
FCT007 Factor Vii Deficiency 67 0.024
480
CRB039 Cerebrovascular Disease 67 0.024
481
MYC006 Mycosis Fungoides 66 0.024
482
OST159 Osteogenic Sarcoma 66 0.024
483
P MCR115 Microvascular Complications of Diabetes 5 66 0.024
484
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.024
485
HYP056 Hypoglycemia 66 0.024
486
c SML038 Small Cell Cancer of the Lung 65 0.024
487
P CNJ013 Conjunctivitis 65 0.024
488
P LPS002 Liposarcoma 65 0.024
489
MRK001 Merkel Cell Carcinoma 65 0.024
490
P DBT009 Diabetes Mellitus 64 0.024
491
ALS001 Alstrom Syndrome 64 0.024
492
HYP020 Hyperprolactinemia 64 0.024
493
LSH001 Leishmaniasis 63 0.024
494
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.024
495
TYP007 Typhoid Fever 63 0.024
496
PLG002 Plague 63 0.024
497
c MLG084 Malignant Fibrous Histiocytoma 63 0.024
498
P CRN300 Coronary Heart Disease 1 63 0.024
499
ACT119 Acute Promyelocytic Leukemia 63 0.024
500
HYP780 Hypoadrenocorticism, Familial 63 0.024
501
P LMY004 Leiomyosarcoma 63 0.024
502
c FNC043 Fanconi Anemia, Complementation Group E 62 0.024
503
c BRN108 Branchiootic Syndrome 1 62 0.024
504
TKY002 Takayasu Arteritis 62 0.024
505
MSL001 Measles 62 0.024
507
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.024
508
VRL011 Viral Infectious Disease 61 0.024
509
P HMN010 Hemangioma 61 0.024
510
SPN186 Spinal Cord Injury 60 0.024
511
DPH001 Diphtheria 60 0.024
512
CRD223 Cardiac Arrhythmia 60 0.024
513
DNG002 Dengue Hemorrhagic Fever 60 0.024
514
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.024
515
P CTR002 Cataract 60 0.024
516
QFV001 Q Fever 60 0.024
517
STT001 Status Epilepticus 60 0.024
518
c ACT071 Acute Kidney Failure 60 0.024
519
P RBL001 Rubella 59 0.024
520
P EPS003 Episodic Ataxia 59 0.024
521
P MCR010 Microcephaly 59 0.024
522
P BND020 Bone Disease 59 0.024
523
PNM001 Pneumocystosis 59 0.024
524
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.024
525
P PLY006 Polydactyly 59 0.024
526
ALP097 Alopecia Universalis Congenita 59 0.024
527
P SYP003 Syphilis 58 0.024
528
P ANP001 Anaplastic Large Cell Lymphoma 58 0.024
529
ISC004 Ischemia 58 0.024
530
c BNG091 Benign Chronic Pemphigus 58 0.024
531
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 58 0.024
532
P MMP001 Mumps 58 0.024
533
CNS004 Constipation 58 0.024
534
c DWL002 Dowling-Degos Disease 1 58 0.024
535
P PRP019 Peripheral Nervous System Disease 58 0.024
536
P INF032 Infertility 57 0.024
537
IRN002 Iron Metabolism Disease 57 0.024
538
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.024
539
MNR012 Meniere Disease 57 0.024
540
DSS009 Disseminated Intravascular Coagulation 57 0.024
541
THR024 Thrombosis 57 0.024
542
THY022 Thymic Carcinoma 57 0.024
543
APH002 Aphasia 57 0.024
544
CMM005 Common Cold 57 0.024
545
BLR008 Bilirubin Metabolic Disorder 57 0.024
546
SCH014 Schistosomiasis 57 0.024
547
P PLY018 Polycythemia 56 0.024
548
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.024
549
SFT003 Soft Tissue Sarcoma 56 0.024
550
AGN016 Aging 56 0.024
551
HPT022 Hepatoblastoma 56 0.024
552
c FML035 Familial Hyperlipidemia 55 0.024
553
VSC003 Visceral Leishmaniasis 55 0.024
554
P GRV001 Graves' Disease 55 0.024
555
P PTT006 Pituitary Adenoma 55 0.024
556
HDR002 Hidradenitis Suppurativa 55 0.024
557
ESN005 Eosinophilic Gastroenteritis 55 0.024
558
P SLM003 Salmonellosis 55 0.024
559
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.024
560
RSC001 Rosacea 54 0.024
561
AMN003 Amnestic Disorder 54 0.024
562
GLC003 Glucose Intolerance 54 0.024
563
RLP001 Relapsing Polychondritis 54 0.024
564
TND005 Tendinitis 54 0.024
565
PLM010 Pulmonary Edema 54 0.024
566
ANL018 Analbuminemia 54 0.024
567
P ART021 Arteriosclerosis 54 0.024
568
LYM040 Lymphoblastic Lymphoma 54 0.024
569
PTT009 Pituitary Gland Disease 54 0.024
570
SLP001 Sleeping Sickness 54 0.024
571
PRS045 Prostatic Hypertrophy 53 0.024
572
TRC023 Trichinosis 53 0.024
573
P EPD016 Epidermolysis Bullosa 53 0.024
574
P INS002 in Situ Carcinoma 53 0.024
575
KRT006 Keratoconjunctivitis 53 0.024
576
PRP036 Peripheral T-Cell Lymphoma 53 0.024
577
P HML001 Hemolytic-Uremic Syndrome 53 0.024
578
P CTN003 Cutaneous Lupus Erythematosus 53 0.024
579
P PTS002 Ptosis 53 0.024
580
c XNT010 Xanthinuria, Type I 53 0.024
581
INT075 Intracranial Hypertension 53 0.024
582
c HPT007 Hepatitis E 53 0.024
583
P RTN018 Retinal Disease 53 0.024
584
c CNT035 Central Nervous System Disease 52 0.024
585
PRP016 Paraplegia 52 0.024
586
ART140 Arteries, Anomalies of 52 0.024
587
P SPP010 Suppressor of Tumorigenicity 3 51 0.024
588
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.024
589
PRS021 Prostatic Adenoma 51 0.024
590
c PNC106 Pancreatic Agenesis 1 51 0.024
591
THR016 Thrombophlebitis 51 0.024
592
ASP003 Aseptic Meningitis 51 0.024
593
RSD004 Rosai-Dorfman Disease 51 0.024
594
ACT017 Acute Chest Syndrome 51 0.024
595
INT071 Intestinal Perforation 51 0.024
596
CHR005 Chorioamnionitis 51 0.024
597
PLR008 Pleurisy 50 0.024
598
P OVR082 Overgrowth Syndrome 50 0.024
599
P ESN008 Eosinophilic Pneumonia 50 0.024
600
AZS001 Azoospermia 50 0.024
601
FSC004 Fasciitis 50 0.024
602
STM007 Stomatitis 50 0.024
603
CHR078 Chorioretinitis 50 0.024
604
c INF145 Infantile Liver Failure Syndrome 1 50 0.024
605
CYT005 Cytomegalovirus Retinitis 50 0.024
606
MLL001 Molluscum Contagiosum 50 0.024
607
c AMY009 Amyloidosis Aa 50 0.024
608
TRY001 Trypanosomiasis 50 0.024
609
NTR046 Neutrophil Migration 50 0.024
610
P OBS001 Obstructive Jaundice 50 0.024
611
HMG002 Hemoglobinuria 50 0.024
612
DYS073 Dysphagia 50 0.024
613
PPL021 Papilledema 49 0.024
614
KRT001 Keratoconjunctivitis Sicca 49 0.024
615
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 49 0.024
616
PRS129 Prostatic Hyperplasia, Benign 49 0.024
617
CHL004 Cholelithiasis 49 0.024
618
DDN006 Duodenitis 49 0.024
619
c INV001 Invasive Aspergillosis 49 0.024
620
HST010 Histiocytosis 48 0.024
621
QDR001 Quadriplegia 48 0.024
622
ADR016 Adrenal Cortical Carcinoma 48 0.024
623
c BCT013 Bacterial Pneumonia 48 0.024
624
BNR002 Bone Resorption Disease 48 0.024
625
CHL061 Childhood Leukemia 48 0.024
626
CRY014 Cryptococcal Meningitis 48 0.024
627
CLC006 Calcinosis 48 0.024
628
VTM033 Vitamin K Deficiency Bleeding 48 0.024
629
PNC034 Pancreas Disease 48 0.024
630
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.024
631
ESN015 Eosinophilic Fasciitis 48 0.024
632
CLN019 Colonic Disease 47 0.024
633
PRC003 Proctitis 47 0.024
634
NRN001 Neuroendocrine Carcinoma 47 0.024
635
RNL077 Renal Fibrosis 47 0.024
636
RTC005 Reticulosarcoma 47 0.024
637
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.024
638
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.024
639
RTN023 Retinitis 46 0.024
640
LPD004 Lipoid Nephrosis 46 0.024
641
P LPC002 Lip Cancer 46 0.024
642
CHR008 Choroiditis 46 0.024
643
P MYC033 Myoclonus 46 0.024
644
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.024
645
P OCY003 Oocyte Maturation Defect 1 45 0.024
646
APL023 Aplasia Cutis Congenita, Nonsyndromic 45 0.024
647
PRT019 Protein-Losing Enteropathy 45 0.024
648
c PLM170 Pulmonary Venoocclusive Disease 1, Autosomal Dominant 45 0.024
649
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.024
650
ASP026 Asplenia, Isolated Congenital 44 0.024
651
c DRM054 Dermatitis, Atopic, 2 44 0.024
652
NDL001 Nodular Malignant Melanoma 44 0.024
653
P FBR003 Fibrous Histiocytoma 44 0.024
654
ART006 Arthus Reaction 44 0.024
655
CVD001 Covid-19 44 0.024
656
MYX004 Myxedema 43 0.024
657
TST015 Testicular Disease 43 0.024
658
HYP084 Hypopyon 43 0.024
659
PLM019 Pleomorphic Liposarcoma 43 0.024
660
P PLN008 Peeling Skin Syndrome 43 0.024
661
ORL015 Oral Squamous Cell Carcinoma 43 0.024
662
DRG002 Drug-Induced Hepatitis 43 0.024
663
DSC009 Discoid Lupus Erythematosus 42 0.024
664
BNS003 Binswanger's Disease 42 0.024
665
P AVS003 Avascular Necrosis 42 0.024
666
P CRN035 Cranial Nerve Palsy 42 0.024
667
CLL021 Collagenous Colitis 42 0.024
668
P PLM025 Pulmonary Venoocclusive Disease 42 0.024
669
DRG024 Drug Allergy 42 0.024
670
c CHR576 Chronic Beryllium Disease 42 0.024
671
OBS082 Obstructive Nephropathy 42 0.024
672
LYM042 Lymphocytic Colitis 41 0.024
673
P KLZ004 Kala-Azar 1 41 0.024
674
49X006 49, Xxxxy Syndrome 41 0.024
675
LYM010 Lymph Node Tuberculosis 41 0.024
676
P RRH023 Rare Hereditary Hemochromatosis 41 0.024
677
MNT303 Mental Retardation, X-Linked, Syndromic, Cabezas Type 41 0.024
678
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.024
679
FNG016 Fungal Keratitis 40 0.024
680
ANG049 Angioedema Induced by Ace Inhibitors 40 0.024
681
P BRY005 Beryllium Disease 40 0.024
682
IMM001 Immune-Complex Glomerulonephritis 40 0.024
683
NDL003 Nodular Nonsuppurative Panniculitis 39 0.024
684
TST004 Testicular Lymphoma 39 0.024
685
c ACT004 Acute Diarrhea 39 0.024
686
PMP002 Pemphigoid Gestationis 39 0.024
687
ENT001 Enterocele 39 0.024
688
ADR004 Adrenal Cortical Adenocarcinoma 39 0.024
689
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.024
690
c CHR682 Chronic Bilirubin Encephalopathy 39 0.024
691
ANT019 Anterograde Amnesia 38 0.024
692
ALL014 Allergic Encephalomyelitis 38 0.024
693
c ATM075 Autoimmune Encephalitis 38 0.024
694
ORF044 Orofacial Granulomatosis 38 0.024
695
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.024
696
HRT040 Hirata Disease 38 0.024
697
P PST059 Pustular Psoriasis 37 0.024
698
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 37 0.024
699
MSC190 Muscular Disease 37 0.024
700
PRR013 Prurigo Nodularis 36 0.024
701
PDT025 Pediatric Multiple Sclerosis 36 0.024
702
ADH001 Adhesions of Uterus 36 0.024
703
HMN004 Hemangioma of Liver 36 0.024
704
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.024
705
c ATM112 Autoimmune Hepatitis Type 1 35 0.024
706
CHR178 Chromosomal Triplication 35 0.024
707
END072 Endotheliitis 35 0.024
708
c ATM021 Autoimmune Inner Ear Disease 34 0.024
709
DDN009 Duodenal Obstruction 34 0.024
710
GNG006 Gingival Hypertrophy 34 0.024
711
ATY022 Atypical Coarctation of Aorta 34 0.024
712
HMN016 Hemangioendothelioma 34 0.024
713
GST014 Gastrointestinal Lymphoma 34 0.024
714
CMP040 Complement Component 4, Partial Deficiency of 33 0.024
715
MLK004 Malakoplakia 33 0.024
716
EPG003 Epiglottitis 33 0.024
717
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.024
718
TTH030 Teeth, Supernumerary 33 0.024
719
VRS001 Virus Associated Hemophagocytic Syndrome 32 0.024
720
HYP193 Hypocomplementemic Urticarial Vasculitis 32 0.024
721
HSH004 Hashimoto Encephalopathy 32 0.024
722
ALP048 Alopecia Totalis 32 0.024
723
MYC014 Mycobacterium Chelonae 31 0.024
724
VLV008 Vulvitis 31 0.024
725
ASH001 Asherman's Syndrome 31 0.024
726
CYT004 Cytomegalic Inclusion Disease 31 0.024
727
JJN008 Jejunoileitis 31 0.024
728
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.024
729
c INF085 Inflammatory Bowel Disease 27 31 0.024
730
DFF031 Diffuse Alveolar Hemorrhage 30 0.024
732
c JVN038 Juvenile Myasthenia Gravis 30 0.024
733
GRN006 Granulomatous Angiitis 30 0.024
734
PMP009 Pemphigus Erythematosus 30 0.024
735
NPH001 Nephrogenic Adenoma 30 0.024
736
c CHR094 Chronic Polyneuropathy 29 0.024
737
PRX008 Paroxysmal Cold Hemoglobinuria 29 0.024
738
SYN092 Syndromic X-Linked Intellectual Disability Cabezas Type 28 0.024
739
TBL025 Tubulointerstitial Nephritis with Uveitis 28 0.024
740
c INF075 Inflammatory Bowel Disease 16 28 0.024
741
RHM013 Rheumatoid Nodulosis 28 0.024
742
ATH004 Athetosis 28 0.024
743
CTN019 Cutaneous Polyarteritis Nodosa 27 0.024
744
ARG004 Argyria 27 0.024
745
CYT018 Cytochrome P450 2d6 Variant 27 0.024
746
DFF015 Diffuse Glomerulonephritis 26 0.024
747
DFF010 Diffuse Alopecia Areata 26 0.024
748
THY006 Thymus Lymphoma 26 0.024
749
FTL073 Fetal Anticonvulsant Syndrome 26 0.024
750
PRD003 Periodontosis 26 0.024
751
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.024
752
VSC052 Vasculitis, Lymphocytic, Nodular 25 0.024
753
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.024
754
c PSR027 Psoriasis 6 25 0.024
755
c MLT009 Multiple Cranial Nerve Palsy 25 0.024
756
PLY179 Polyomavirus-Associated Nephropathy 24 0.024
757
SRP002 Serpiginous Choroiditis 24 0.024
758
HMP028 Hemophagocytic Syndrome Associated with an Infection 24 0.024
759
c MLT094 Multiple Sclerosis 3 24 0.024
760
HPT066 Hepatoportal Sclerosis 23 0.024
762
ULC008 Ulcerative Proctitis 23 0.024
763
THR116 Thrombocytopenia, Cyclic 22 0.024
764
IRV001 Irvan Syndrome 22 0.024
765
PRL021 Perilymphatic Fistula 22 0.024
766
INS015 Inosine Triphosphatase Deficiency 22 0.024
767
PRG110 Progressive Encephalomyelitis with Rigidity and Myoclonus 21 0.024
768
P ACQ041 Acquired Amegakaryocytic Thrombocytopenia 21 0.024
769
BNT001 Banti's Syndrome 21 0.024
770
ALK017 Alk-Positive Large B-Cell Lymphoma 20 0.024
771
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 19 0.024
772
c INF152 Infectious Posterior Uveitis 19 0.024
773
PMP013 Pemphigus Gestationis 19 0.024
774
c CHR686 Chronic Cutaneous Lupus Erythematosus 19 0.024
775
c MLT095 Multiple Sclerosis 4 19 0.024
776
c NNN032 Non-Infectious Posterior Uveitis 19 0.024
777
PRM314 Primary Cutaneous Lymphoma 18 0.024
778
HHV001 Hhv-6 Encephalitis 18 0.024
779
c THP005 Thiopurines, Poor Metabolism of, 2 17 0.024
780
CLS055 Classic Pyoderma Gangrenosum 16 0.024
781
BLL018 Bullous Pyoderma Gangrenosum 16 0.024
782
GRN020 Granulomatous Hypophysitis 15 0.024
783
c INF151 Infectious Panuveitis 14 0.024
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