Search results for Tacrolimus

1275 hits were found for Tacrolimus

# Family MCID Name MIFTS Score
1
TCR004 Tacrolimus Dose Selection 13 2.739
2
OBS346 Obsolete: Resistance to Tacrolimus in Transplantation 1 2.739
3
P GRF003 Graft-Versus-Host Disease 71 0.452
4
P DRM053 Dermatitis, Atopic 66 0.415
5
DRM006 Dermatitis 61 0.399
6
c ACT135 Acute Graft Versus Host Disease 51 0.314
7
P KDN018 Kidney Disease 70 0.306
8
P LKM002 Leukemia 66 0.294
9
P LYM118 Lymphoma 68 0.265
10
HML018 Homologous Wasting Disease 22 0.263
11
LYM019 Lymphosarcoma 47 0.258
12
MYL009 Myelodysplastic Syndrome 70 0.257
13
P MYL006 Myeloid Leukemia 60 0.253
14
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.239
15
c LKM061 Leukemia, Acute Myeloid 83 0.238
16
P LYM031 Lymphocytic Leukemia 55 0.238
17
P LPS004 Lupus Erythematosus 61 0.235
18
P NPH012 Nephrotic Syndrome 63 0.233
19
c SYS001 Systemic Lupus Erythematosus 86 0.232
20
ADL002 Adult Syndrome 69 0.225
21
P LKM062 Leukemia, Acute Lymphoblastic 68 0.225
22
HMT002 Hematologic Cancer 62 0.222
23
c CHR417 Chronic Graft Versus Host Disease 56 0.222
24
c LKM063 Leukemia, Chronic Myeloid 71 0.218
25
ULC004 Ulcerative Colitis 73 0.218
26
END030 End Stage Renal Failure 58 0.217
27
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.215
28
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.210
29
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.210
30
c PRM038 Primary Agammaglobulinemia 43 0.208
31
CLT003 Colitis 62 0.206
32
LYM040 Lymphoblastic Lymphoma 54 0.201
33
LYM133 Lymphoma, Hodgkin, Classic 69 0.197
34
c LKM071 Leukemia, Chronic Lymphocytic 79 0.194
35
MYL069 Myeloma, Multiple 85 0.193
36
P LCH002 Lichen Planus 54 0.193
37
PLS009 Plasma Cell Neoplasm 51 0.193
38
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.185
39
SKN016 Skin Disease 63 0.182
40
c CHR064 Chronic Monocytic Leukemia 34 0.180
41
CYT008 Cytomegalovirus Infection 56 0.179
42
P TRM003 Tremor 53 0.179
43
c CHR684 Chronic Kidney Disease 66 0.176
44
ATM095 Autoimmune Disease 61 0.176
45
P PSR002 Psoriasis 62 0.174
46
PST011 Pustulosis of Palm and Sole 52 0.174
47
P GLM007 Glomerulonephritis 57 0.173
48
MYL031 Myeloproliferative Neoplasm 65 0.172
49
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.172
50
P MMB011 Membranous Nephropathy 50 0.172
51
P MYS003 Myasthenia Gravis 68 0.171
52
P DRR001 Diarrhea 57 0.169
53
BNM001 Bone Marrow Cancer 43 0.169
54
DFC004 Deficiency Anemia 75 0.168
55
KRT006 Keratoconjunctivitis 53 0.167
56
c HPT001 Hepatitis C 63 0.165
57
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.165
58
c DRM054 Dermatitis, Atopic, 2 45 0.163
59
P NTR004 Neutropenia 63 0.162
60
P HPT021 Hepatitis 67 0.161
61
P LYM033 Lymphoproliferative Syndrome 60 0.160
62
P BCL017 B-Cell Lymphoma 58 0.160
63
P DBT009 Diabetes Mellitus 64 0.158
64
P LVR013 Liver Disease 68 0.157
65
P RHM011 Rheumatoid Arthritis 80 0.156
66
c HPT073 Hepatitis C Virus 70 0.156
67
MNT001 Mantle Cell Lymphoma 66 0.156
68
c RHB024 Rhabdomyosarcoma 2 65 0.153
69
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.152
70
P ENC018 Encephalopathy 61 0.152
71
P FLL037 Follicular Lymphoma 66 0.151
72
PST046 Post-Transplant Lymphoproliferative Disease 53 0.151
73
PYD002 Pyoderma 51 0.151
74
c HYP836 Hypercholesterolemia, Familial, 1 72 0.149
75
HYP066 Hyperglycemia 61 0.149
76
c FLL041 Follicular Lymphoma 1 49 0.149
77
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.149
78
MYL005 Myelofibrosis 67 0.148
79
CYT002 Cytokine Deficiency 44 0.148
80
ORL013 Oral Lichen Planus 45 0.146
81
48X005 48,xyyy 39 0.146
82
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.144
83
PYD001 Pyoderma Gangrenosum 54 0.144
84
c HYP595 Hypertension, Essential 84 0.142
85
BRK010 Burkitt Lymphoma 67 0.142
86
P CHR285 Chronic Myelomonocytic Leukemia 59 0.142
87
THR123 Thrombotic Microangiopathy 38 0.142
88
CRH001 Crohn's Disease 74 0.141
89
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.141
90
P FCL005 Focal Segmental Glomerulosclerosis 58 0.139
91
c ACT073 Acute Leukemia 58 0.138
92
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.136
93
LPD008 Lipid Metabolism Disorder 62 0.133
94
P ART022 Arthritis 70 0.132
95
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.132
96
PLS025 Plasmablastic Lymphoma 47 0.132
97
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.132
98
P ALP008 Alopecia 56 0.130
99
P INF037 Inflammatory Bowel Disease 56 0.130
100
MRG003 Marginal Zone B-Cell Lymphoma 53 0.130
101
P SRC025 Sarcoidosis 1 70 0.129
102
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.127
103
BRN002 Bronchiolitis 59 0.127
104
BRN012 Bronchiolitis Obliterans 56 0.126
105
P DRM010 Dermatomyositis 61 0.124
106
LNG099 Lung Disease 61 0.124
107
P CNJ013 Conjunctivitis 65 0.122
108
VRN004 Vernal Keratoconjunctivitis 47 0.122
109
P TRN020 Turner Syndrome 65 0.121
110
P APL001 Aplastic Anemia 74 0.119
111
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.119
112
HDG004 Hodgkin's Granuloma 26 0.119
113
HDG006 Hodgkin's Paragranuloma 24 0.119
114
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.117
115
P CNR004 Cone-Rod Dystrophy 2 71 0.116
116
LYM012 Lymphoplasmacytic Lymphoma 61 0.116
117
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.116
118
CNT047 Contact Dermatitis 57 0.116
119
MCS002 Mucositis 55 0.116
120
SPL004 Splenic Marginal Zone Lymphoma 51 0.116
121
ATX019 Ataxia with Vitamin E Deficiency 48 0.116
122
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.114
123
GNG012 Gingival Overgrowth 51 0.114
124
MCR004 Macroglobulinemia 50 0.114
125
ATY042 Atypical Chronic Myeloid Leukemia 49 0.112
126
LCH016 Lichen Sclerosus Et Atrophicus 41 0.112
127
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.110
128
P HML001 Hemolytic-Uremic Syndrome 52 0.110
129
P THR014 Thrombocytopenia 68 0.108
130
ALL026 Allergic Hypersensitivity Disease 64 0.108
132
MYC006 Mycosis Fungoides 66 0.106
133
ISC004 Ischemia 60 0.106
134
LPD004 Lipoid Nephrosis 47 0.106
135
SKN005 Skin Atrophy 43 0.106
136
LVR012 Liver Cirrhosis 63 0.105
137
SZR001 Sezary's Disease 60 0.105
138
P PLY041 Polymyositis 57 0.105
139
GLC003 Glucose Intolerance 54 0.105
140
P TCL004 T-Cell Leukemia 47 0.105
141
P EXN002 Exanthem 57 0.103
142
RFR010 Refractory Anemia 48 0.103
143
P UVT001 Uveitis 57 0.101
144
c ADL017 Adult T-Cell Leukemia 57 0.101
145
c FML035 Familial Hyperlipidemia 55 0.101
146
P HYP077 Hypertrichosis 50 0.101
147
ALL009 Allergic Conjunctivitis 50 0.101
148
CHL079 Children's Interstitial Lung Disease 27 0.101
149
INT066 Interstitial Lung Disease 59 0.099
150
c ACT071 Acute Kidney Failure 59 0.099
151
P OVR082 Overgrowth Syndrome 50 0.099
152
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.099
153
P SKN015 Skin Carcinoma 67 0.096
154
c ATM011 Autoimmune Hepatitis 62 0.096
155
LYM051 Lymphomatoid Granulomatosis 45 0.096
156
KRT019 Keratitis, Hereditary 67 0.094
157
RSC001 Rosacea 55 0.094
158
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.094
159
VRL011 Viral Infectious Disease 61 0.092
160
IGG001 Iga Glomerulonephritis 48 0.092
161
ATP013 Atopic Keratoconjunctivitis 41 0.092
162
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.090
163
c FNC043 Fanconi Anemia, Complementation Group E 62 0.090
164
P VSC011 Vasculitis 62 0.090
165
P HYP750 Hypertriglyceridemia, Familial 61 0.090
166
ALL010 Allergic Contact Dermatitis 55 0.090
167
HRY003 Hairy Cell Leukemia 55 0.090
168
TXC002 Toxic Encephalopathy 52 0.090
169
CYT018 Cytochrome P450 2d6 Variant 27 0.090
170
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.088
171
HPT046 Hepatic Veno-Occlusive Disease 56 0.088
172
P NRP001 Neuropathy 56 0.088
173
PRP030 Purpura 55 0.088
174
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.088
175
c MCR113 Microvascular Complications of Diabetes 3 52 0.088
176
PRL017 Prolymphocytic Leukemia 47 0.088
177
CHR286 Chronic Neutrophilic Leukemia 41 0.088
178
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.088
179
IMM167 Immune Deficiency Disease 78 0.085
180
DWN001 Down Syndrome 70 0.085
181
P PNM007 Pneumonia 68 0.085
182
HYP056 Hypoglycemia 66 0.085
183
BLL006 Bullous Pemphigoid 62 0.085
184
c CHR418 Chronic Leukemia 50 0.085
185
PLY001 Polycythemia Vera 69 0.083
186
P ESS003 Essential Thrombocythemia 67 0.083
187
P THY023 Thymoma 65 0.083
188
P MYP004 Myopathy 64 0.083
189
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.083
190
P CYS018 Cystitis 59 0.083
191
P BND020 Bone Disease 59 0.083
192
DFF005 Diffuse Large B-Cell Lymphoma 56 0.083
193
P PLY018 Polycythemia 55 0.083
194
c THY107 Thymoma, Familial 54 0.083
195
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.083
196
c PRM012 Primary Polycythemia 52 0.083
197
c THR090 Thrombocythemia 1 49 0.083
198
CHR563 Chronic Eosinophilic Leukemia 48 0.083
199
c MCR120 Microvascular Complications of Diabetes 7 47 0.083
200
c MCR130 Microvascular Complications of Diabetes 6 41 0.083
201
c MCR133 Microvascular Complications of Diabetes 4 41 0.083
202
P HPT023 Hepatocellular Carcinoma 100 0.080
203
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.080
204
c HPT003 Hepatitis a 63 0.080
205
P HML002 Hemolytic Anemia 62 0.080
206
P CTR002 Cataract 60 0.080
207
EYD002 Eye Disease 58 0.080
208
TLN003 Telangiectasis 51 0.080
209
P PRR002 Pure Red-Cell Aplasia 48 0.080
210
RDC006 Red Cell Aplasia 42 0.080
211
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.078
212
CYS001 Cystic Fibrosis 80 0.078
213
P NRF023 Neurofibromatosis, Type Ii 76 0.078
214
P HYP098 Hypereosinophilic Syndrome 66 0.078
215
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.078
216
P ALP009 Alopecia Areata 60 0.078
217
P HDC001 Headache 57 0.078
218
P PMP001 Pemphigus 55 0.078
219
P CTN003 Cutaneous Lupus Erythematosus 52 0.078
220
PLS016 Plasma Cell Leukemia 46 0.078
221
P SBR004 Seborrheic Dermatitis 45 0.078
222
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.078
223
CYT004 Cytomegalic Inclusion Disease 31 0.078
224
c ACT068 Acute Cystitis 63 0.075
225
CHL068 Cholestasis 60 0.075
226
P OPT006 Optic Nerve Disease 57 0.075
227
c PSR017 Psoriasis 2 52 0.075
228
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.075
229
c PSR023 Psoriasis 1 49 0.075
230
RTC005 Reticulosarcoma 49 0.075
231
PRC003 Proctitis 47 0.075
232
ACT003 Acute Kidney Tubular Necrosis 45 0.075
233
c PSR028 Psoriasis 7 39 0.075
234
c PSR032 Psoriasis 11 38 0.075
235
c PSR018 Psoriasis 13 38 0.075
236
CHR463 Chronic Actinic Dermatitis 37 0.075
237
c INF071 Inflammatory Bowel Disease 1 68 0.073
238
P HYP061 Hypertrophic Cardiomyopathy 66 0.073
239
P ANP001 Anaplastic Large Cell Lymphoma 61 0.073
240
c BNG091 Benign Chronic Pemphigus 59 0.073
241
P CRD246 Cardiovascular System Disease 56 0.073
242
P MYS005 Myositis 56 0.073
243
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.073
244
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.073
245
P CHL066 Cholangitis 50 0.073
246
FDL002 Food Allergy 49 0.073
247
ACT011 Acute Contagious Conjunctivitis 40 0.073
248
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.073
249
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.073
250
KPS004 Kaposi Sarcoma 75 0.070
251
c ATR087 Atrial Standstill 1 74 0.070
252
P HRP006 Herpes Simplex 65 0.070
253
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.070
254
GST045 Gastroenteritis 59 0.070
255
BCT022 Bacterial Infectious Disease 56 0.070
256
P PLY019 Polyneuropathy 56 0.070
257
RHM027 Rheumatic Disease 56 0.070
258
LTH001 Lethal Midline Granuloma 43 0.070
259
DSC009 Discoid Lupus Erythematosus 42 0.070
260
BLN010 Balanitis 36 0.070
261
RFR002 Refractory Hairy Cell Leukemia 32 0.070
262
CLS052 Classic Hairy Cell Leukemia 27 0.070
263
BND002 B- and T-Cell Mixed Leukemia 18 0.070
264
P SYS005 Systemic Scleroderma 70 0.067
265
P MCR115 Microvascular Complications of Diabetes 5 66 0.067
266
P ASP006 Aspergillosis 66 0.067
267
SRC014 Sarcoma 65 0.067
268
P PRM006 Primary Biliary Cirrhosis 61 0.067
269
HRP004 Herpes Zoster 60 0.067
270
c ACT027 Acute Pancreatitis 59 0.067
271
P SZR006 Seizure Disorder 58 0.067
272
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.067
273
PNM001 Pneumocystosis 54 0.067
274
SPN035 Spindle Cell Sarcoma 51 0.067
275
P CTN015 Cutaneous T Cell Lymphoma 49 0.067
276
c FCL025 Focal Segmental Glomerulosclerosis 1 47 0.067
277
c SYS043 Systemic Lupus Erythematosus 1 38 0.067
278
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.067
279
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.064
280
CNN005 Connective Tissue Disease 66 0.064
281
c MCR129 Microvascular Complications of Diabetes 1 66 0.064
282
MGK001 Megakaryocytic Leukemia 64 0.064
283
P CRN018 Coronary Artery Anomaly 63 0.064
284
c LCL006 Localized Scleroderma 62 0.064
285
P THL005 Thalassemia 60 0.064
286
HMG005 Hemoglobinopathy 55 0.064
287
CRH005 Crohn's Colitis 52 0.064
288
c MLG054 Malignant Histiocytosis 50 0.064
289
KRT001 Keratoconjunctivitis Sicca 50 0.064
290
ENT004 Enthesopathy 48 0.064
291
INT054 Intraocular Lymphoma 48 0.064
292
FLL008 Folliculitis 46 0.064
293
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.064
294
c MCR112 Microvascular Complications of Diabetes 2 41 0.064
295
IDP091 Idiopathic Nephrotic Syndrome 38 0.064
296
AST005 Asthma 77 0.060
297
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 0.060
298
P ENC004 Encephalitis 61 0.060
299
P PNC044 Pancreatitis 61 0.060
300
c HPT016 Hepatitis B 59 0.060
301
VSL002 Visual Epilepsy 58 0.060
302
P CND004 Candidiasis 57 0.060
303
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.060
304
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.060
305
IMP005 Impotence 52 0.060
306
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.060
307
THR004 Thrombocytosis 51 0.060
308
c ACT134 Acute Liver Failure 51 0.060
309
P SCK005 Sickle Cell Disease 50 0.060
310
CCT002 Cicatricial Pemphigoid 50 0.060
311
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.060
312
P SCL009 Sclerosing Cholangitis 47 0.060
313
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.060
314
RNL077 Renal Fibrosis 47 0.060
315
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.060
316
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.060
317
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.060
318
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.060
319
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.060
320
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.060
321
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.060
322
PCH007 Pouchitis 39 0.060
323
LYM005 Lymphocele 35 0.060
324
c BKV001 Bk-Virus Nephropathy 23 0.060
325
P RSP003 Respiratory Failure 74 0.057
326
SCK003 Sickle Cell Anemia 72 0.057
327
CNG034 Congestive Heart Failure 70 0.057
328
c PRC016 Pre-Eclampsia 63 0.057
329
P HYP069 Hyperparathyroidism 62 0.057
330
c ANM038 Anemia, Autoimmune Hemolytic 61 0.057
331
NTR005 Nutritional Deficiency Disease 61 0.057
332
PRT013 Portal Hypertension 60 0.057
333
P URT039 Urticaria 58 0.057
334
LYM027 Lymphopenia 57 0.057
335
ERY051 Erythroleukemia, Familial 56 0.057
336
MLL001 Molluscum Contagiosum 49 0.057
337
47X002 47,xyy 49 0.057
338
KRT008 Keratopathy 46 0.057
339
MTS001 Mutism 45 0.057
340
c CHR682 Chronic Bilirubin Encephalopathy 38 0.057
341
NCR002 Necrobiosis Lipoidica 38 0.057
342
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.057
343
ERS002 Erosive Pustular Dermatosis of the Scalp 23 0.057
344
ULC008 Ulcerative Proctitis 23 0.057
345
P BRS047 Breast Cancer 96 0.053
346
P HRT032 Heart Disease 75 0.053
347
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.053
348
P AMY004 Amyloidosis 70 0.053
349
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.053
350
MSC007 Muscle Hypertrophy 63 0.053
351
DPR016 Depression 63 0.053
352
c ALP101 Alpha-Thalassemia 62 0.053
353
P KDN017 Kidney Cancer 61 0.053
354
SQM006 Squamous Cell Carcinoma 60 0.053
355
CHC001 Chickenpox 60 0.053
356
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.053
357
c CHL119 Cholangitis, Primary Sclerosing 57 0.053
358
MNT002 Mental Depression 57 0.053
359
P SJG008 Sjogren Syndrome 56 0.053
360
PLS011 Plasmacytoma 56 0.053
361
SFT003 Soft Tissue Sarcoma 56 0.053
362
AGN016 Aging 56 0.053
363
HYP005 Hypokalemia 55 0.053
364
OCL020 Ocular Cicatricial Pemphigoid 54 0.053
365
P ICH004 Ichthyosis 54 0.053
366
PNC001 Pancytopenia 54 0.053
367
c LKM070 Leukemia, Acute Monocytic 53 0.053
368
PRP036 Peripheral T-Cell Lymphoma 53 0.053
369
c VRL010 Viral Hepatitis 51 0.053
370
ILS001 Ileus 51 0.053
371
MTB004 Metabolic Acidosis 50 0.053
372
BLR001 Biliary Atresia 50 0.053
373
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.053
374
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.053
375
SKN013 Skin Benign Neoplasm 49 0.053
376
HMG002 Hemoglobinuria 49 0.053
377
c INV001 Invasive Aspergillosis 48 0.053
378
CHL056 Cheilitis 48 0.053
379
P RNL015 Renal Hypertension 48 0.053
380
EVN001 Evans' Syndrome 46 0.053
381
P PRL003 Proliferative Glomerulonephritis 44 0.053
382
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.053
383
c HYP272 Hypercholesterolemia, Familial, 3 43 0.053
384
LRG008 Large Granular Lymphocyte Leukemia 41 0.053
385
c MLG074 Malignant Mesenchymoma 39 0.053
386
ATM052 Autoimmune Disease 1 37 0.053
387
c SBR001 Seborrheic Infantile Dermatitis 31 0.053
388
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.053
389
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 28 0.053
390
P PRS040 Prostate Cancer 97 0.049
391
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.049
392
c THR092 Thrombophilia Due to Thrombin Defect 73 0.049
393
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.049
394
ANX010 Anxiety 72 0.049
395
SCH036 Scheie Syndrome 71 0.049
396
P DMN001 Diamond-Blackfan Anemia 69 0.049
397
MLN008 Melanoma 69 0.049
398
P MNN013 Meningitis 65 0.049
399
c MCL013 Mucolipidosis Iv 64 0.049
400
IDP011 Idiopathic Interstitial Pneumonia 63 0.049
401
P CRN300 Coronary Heart Disease 1 63 0.049
402
ACT119 Acute Promyelocytic Leukemia 63 0.049
403
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.049
404
P PLM036 Pulmonary Fibrosis 61 0.049
405
P INT143 Interstitial Cystitis 61 0.049
406
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.049
407
GNG013 Gingivitis 59 0.049
408
IGR001 Ige Responsiveness, Atopic 59 0.049
409
PPT005 Peptic Ulcer Disease 58 0.049
410
c DWL002 Dowling-Degos Disease 1 58 0.049
411
PMP006 Pemphigus Vulgaris, Familial 58 0.049
412
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.049
413
ORL005 Oral Candidiasis 56 0.049
414
ACT200 Acute Monoblastic Leukemia 55 0.049
415
P ART021 Arteriosclerosis 54 0.049
416
AMN001 Amenorrhea 54 0.049
417
P MNC007 Monocytic Leukemia 54 0.049
418
KRT009 Keratosis 53 0.049
419
ART140 Arteries, Anomalies of 53 0.049
420
HYP014 Hyperuricemia 51 0.049
421
OCL069 Ocular Motor Apraxia 51 0.049
422
BRN071 Brain Injury 49 0.049
423
BNR002 Bone Resorption Disease 48 0.049
424
ACT098 Acute Erythroid Leukemia 48 0.049
425
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.049
426
KRT013 Keratolytic Winter Erythema 46 0.049
427
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.049
428
GRN007 Granuloma Annulare 45 0.049
429
ANT039 Antisynthetase Syndrome 44 0.049
430
PRS063 Paresthesia 43 0.049
431
SPR126 Superior Semicircular Canal Dehiscence 40 0.049
432
GLM044 Glomerular Disease 39 0.049
433
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.049
434
c HMG029 Hemoglobin Se Disease 38 0.049
435
P ATM020 Autoimmune Enteropathy 35 0.049
436
GNG006 Gingival Hypertrophy 34 0.049
437
SVR055 Severe Immune-Mediated Enteropathy 24 0.049
438
c ADL093 Adult Acute Monocytic Leukemia 20 0.049
439
c DLT002 Dilated Cardiomyopathy 79 0.045
440
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.045
441
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.045
442
P OST002 Osteoporosis 73 0.045
443
c BTT014 Beta-Thalassemia 72 0.045
444
P NRB001 Neuroblastoma 71 0.045
445
P WSK001 Wiskott-Aldrich Syndrome 71 0.045
446
CRB039 Cerebrovascular Disease 69 0.045
447
P MYC084 Mycobacterium Tuberculosis 1 68 0.045
448
c JVN010 Juvenile Rheumatoid Arthritis 67 0.045
449
ATH013 Atherosclerosis Susceptibility 66 0.045
450
P VSC007 Vascular Disease 63 0.045
451
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.045
452
c SCL052 Scleroderma, Familial Progressive 62 0.045
453
P NRM001 Neuromyelitis Optica 60 0.045
454
CHR001 Churg-Strauss Syndrome 60 0.045
455
NTH001 Netherton Syndrome 60 0.045
456
ADL030 Adult-Onset Still's Disease 58 0.045
457
CNS004 Constipation 57 0.045
458
P INF032 Infertility 57 0.045
459
THR024 Thrombosis 56 0.045
460
CMR002 Coumarin Resistance 56 0.045
461
ACT058 Active Peptic Ulcer Disease 55 0.045
462
P ANG015 Angioedema 54 0.045
463
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.045
464
c PST005 Posterior Uveitis 54 0.045
465
P LYM025 Lymphedema 53 0.045
466
P HST010 Histiocytosis 53 0.045
467
GLS018 Glass Syndrome 53 0.045
468
P SHR001 Short Bowel Syndrome 52 0.045
469
P PTS002 Ptosis 52 0.045
470
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.045
471
CRT016 Carotid Artery Disease 52 0.045
472
c ALM001 Al Amyloidosis 50 0.045
473
DYS073 Dysphagia 50 0.045
474
P RNL007 Renal Tubular Acidosis 50 0.045
475
IRR003 Irritant Dermatitis 47 0.045
476
DRY001 Dry Eye Syndrome 47 0.045
477
FRY002 Fryns Syndrome 43 0.045
478
SPC005 Speech Disorder 42 0.045
479
P AVS003 Avascular Necrosis 42 0.045
480
BLP006 Blepharoconjunctivitis 38 0.045
481
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.045
483
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.045
484
ACT162 Acute Sensory Ataxic Neuropathy 26 0.045
485
ESN016 Eosinophilic Pustular Folliculitis 25 0.045
486
HRP008 Herpes Simiae 25 0.045
487
LCH008 Lichen Planus Pigmentosus 21 0.045
488
SVR004 Severe Combined Immunodeficiency 73 0.040
489
SKN019 Skin Melanoma 67 0.040
490
GRN037 Granulomatosis with Polyangiitis 64 0.040
491
INC002 Inclusion Body Myositis 64 0.040
492
GT001 Gout 63 0.040
493
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.040
494
TXC005 Toxic Shock Syndrome 61 0.040
495
FTT001 Fatty Liver Disease 61 0.040
496
CRD223 Cardiac Arrhythmia 60 0.040
497
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.040
498
LNG108 Langerhans Cell Histiocytosis 58 0.040
499
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.040
500
P PRP019 Peripheral Nervous System Disease 57 0.040
501
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.040
502
PPL022 Papilloma 54 0.040
503
c THR045 Thrombotic Thrombocytopenic Purpura, Congenital 54 0.040
504
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.040
505
P EPD016 Epidermolysis Bullosa 53 0.040
506
TRM010 Traumatic Brain Injury 53 0.040
507
P INT068 Intestinal Disease 52 0.040
508
MCN017 Meconium Ileus 52 0.040
509
PRT018 Portal Vein Thrombosis 50 0.040
510
c INF145 Infantile Liver Failure Syndrome 1 50 0.040
511
BLP005 Blepharitis 49 0.040
512
IMP004 Impetigo 49 0.040
513
MYL003 Myeloid Sarcoma 49 0.040
514
PNN001 Panniculitis 49 0.040
515
c NPH049 Nephrotic Syndrome, Type 2 48 0.040
516
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.040
517
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.040
518
MCR225 Macrophage Activation Syndrome 44 0.040
519
SBC016 Subacute Delirium 44 0.040
520
INT253 Intestinal Benign Neoplasm 44 0.040
521
KPS002 Kaposiform Hemangioendothelioma 43 0.040
522
P CRN024 Corneal Disease 43 0.040
523
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.040
524
49X006 49, Xxxxy Syndrome 41 0.040
525
ANG065 Angioma, Tufted 39 0.040
526
SKN006 Skin Sarcoidosis 39 0.040
527
HMR023 Hemorrhagic Cystitis 38 0.040
528
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.040
529
P PST059 Pustular Psoriasis 38 0.040
530
SYS071 Systemic Autoimmune Disease 37 0.040
531
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.040
532
PRR013 Prurigo Nodularis 36 0.040
533
AKN002 Akinetic Mutism 35 0.040
534
SML008 Small Intestine Lymphoma 35 0.040
535
HMN016 Hemangioendothelioma 34 0.040
536
c SBC035 Subacute Cutaneous Lupus Erythematosus 33 0.040
537
ORL022 Oral Erosive Lichen 32 0.040
538
P OVR096 Overlap Myositis 27 0.040
539
ACT118 Acute Non Lymphoblastic Leukemia 27 0.040
540
c ACQ016 Acquired Pure Red Cell Aplasia 26 0.040
541
HYP213 Hypomelanotic Disorder 24 0.040
542
ICH018 Ichthyosis Linearis Circumflexa 13 0.040
543
PLY043 Polyomavirus Allograft Nephropathy 13 0.040
545
STR067 Stroke, Ischemic 80 0.035
546
P BLD134 Bladder Cancer 78 0.035
547
MRF001 Marfan Syndrome 75 0.035
548
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.035
549
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.035
550
P MLT020 Multiple Sclerosis 72 0.035
551
P EPL164 Epilepsy 71 0.035
552
c BSL007 Basal Cell Carcinoma 68 0.035
553
EWN003 Ewing Sarcoma 68 0.035
554
P PLM037 Pulmonary Hypertension 68 0.035
555
P CRN037 Craniosynostosis 68 0.035
556
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 67 0.035
557
FCT007 Factor Vii Deficiency 66 0.035
558
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.035
559
DGR001 Digeorge Syndrome 63 0.035
560
P MST009 Mastocytosis 63 0.035
561
P RHB003 Rhabdomyosarcoma 62 0.035
562
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.035
563
P HMN010 Hemangioma 61 0.035
564
OST003 Osteonecrosis 61 0.035
565
SPN186 Spinal Cord Injury 60 0.035
566
HPT019 Hepatic Encephalopathy 60 0.035
567
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.035
568
ACQ007 Acquired Immunodeficiency Syndrome 60 0.035
569
CHL028 Childhood Type Dermatomyositis 60 0.035
570
P GLL022 Guillain-Barre Syndrome 59 0.035
571
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.035
572
P PLY014 Polycystic Kidney Disease 59 0.035
573
CRY005 Cryptococcosis 58 0.035
574
ERY003 Erythema Multiforme 57 0.035
575
P RHN004 Rhinitis 57 0.035
576
BLR008 Bilirubin Metabolic Disorder 57 0.035
577
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.035
578
HPT022 Hepatoblastoma 56 0.035
579
BRN004 Brain Edema 55 0.035
580
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.035
581
MRD002 Marden-Walker Syndrome 55 0.035
582
CLL003 Cellulitis 54 0.035
583
HMP005 Hemiplegia 54 0.035
584
VLC001 Velocardiofacial Syndrome 54 0.035
585
HNC001 Henoch-Schoenlein Purpura 54 0.035
586
ORP003 Oropharynx Cancer 54 0.035
587
GST037 Gastroparesis 53 0.035
588
c ACT020 Acute T Cell Leukemia 53 0.035
589
CLR030 Clear Cell Renal Cell Carcinoma 53 0.035
590
NRT004 Neuritis 53 0.035
591
INT075 Intracranial Hypertension 53 0.035
592
ALC009 Alcoholic Liver Cirrhosis 53 0.035
593
HYP063 Hypersplenism 53 0.035
594
ACR041 Acromelic Frontonasal Dysostosis 52 0.035
595
DRM011 Dermatophytosis 52 0.035
596
RYS001 Reye Syndrome 51 0.035
597
MSC190 Muscular Disease 51 0.035
598
APR001 Apraxia 51 0.035
599
VSC006 Vascular Cancer 51 0.035
600
MCR088 Microscopic Polyangiitis 51 0.035
601
MYL001 Myelitis 51 0.035
602
P ECL001 Eclampsia 51 0.035
603
HYP081 Hypolipoproteinemia 50 0.035
604
PTT041 Pituitary Stalk Interruption Syndrome 50 0.035
605
ACH005 Achalasia 50 0.035
606
IRD001 Iridocyclitis 50 0.035
607
P PLG001 Pelger-Huet Anomaly 50 0.035
608
STM007 Stomatitis 49 0.035
609
P IGN003 Iga Nephropathy 1 49 0.035
610
INP001 Inappropriate Adh Syndrome 49 0.035
611
PRN014 Paronychia 49 0.035
612
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.035
613
WTH001 Withdrawal Disorder 48 0.035
614
ATS010 Autosomal Recessive Disease 48 0.035
615
CRY014 Cryptococcal Meningitis 48 0.035
616
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.035
617
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.035
618
CRN027 Corneal Neovascularization 47 0.035
619
SYS034 Systemic Onset Juvenile Idiopathic Arthritis 47 0.035
620
c MLG069 Malignant Hypertension 47 0.035
621
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.035
622
MGC001 Megacolon 46 0.035
623
P MYC033 Myoclonus 46 0.035
624
LNT004 Lentigines 46 0.035
625
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 46 0.035
626
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.035
627
EXT010 Extramedullary Plasmacytoma 45 0.035
628
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.035
629
P OVR046 Ovarian Cyst 45 0.035
630
IMM136 Immune System Disease 45 0.035
631
ECZ002 Eczema Herpeticum 44 0.035
632
PTY001 Pityriasis Rosea 44 0.035
633
CNT017 Central Nervous System Origin Vertigo 44 0.035
634
HPT004 Hepatic Coma 43 0.035
635
IDP033 Idiopathic Edema 43 0.035
636
PLY068 Polysubstance Abuse 43 0.035
637
HYP457 Hypertrophic Scars 43 0.035
638
SQM002 Squamous Cell Papilloma 42 0.035
639
DRG002 Drug-Induced Hepatitis 42 0.035
640
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.035
641
P DST107 Distal Renal Tubular Acidosis 41 0.035
642
GGR001 Geographic Tongue 41 0.035
643
CLD014 Cole Disease 41 0.035
644
HMN035 Hemangioma-Thrombocytopenia Syndrome 41 0.035
645
FNG016 Fungal Keratitis 40 0.035
646
GLC008 Glucose Metabolism Disease 40 0.035
647
ACR005 Acrodermatitis 40 0.035
648
ANG049 Angioedema Induced by Ace Inhibitors 40 0.035
649
ENT001 Enterocele 39 0.035
650
TXC001 Toxic Megacolon 39 0.035
651
CRT012 Cortical Blindness 39 0.035
652
PRN039 Paraneoplastic Syndromes 38 0.035
653
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.035
654
CHN040 Choanal Atresia and Lymphedema 36 0.035
655
PSD088 Pseudobulbar Affect 36 0.035
656
VLV008 Vulvitis 31 0.035
657
c NRM008 Neuromyelitis Optica Spectrum Disorder 31 0.035
658
ACN019 Acanthamoeba Keratitis 31 0.035
659
PNC012 Punctate Epithelial Keratoconjunctivitis 30 0.035
660
ENG004 Engraftment Syndrome 30 0.035
661
DLT018 Dilution, Pigmentary 29 0.035
662
PDT027 Pediatric Ulcerative Colitis 28 0.035
663
FTL073 Fetal Anticonvulsant Syndrome 26 0.035
664
ALL012 Allergic Angiitis 24 0.035
666
LPS019 Lupus Erythematosus Tumidus 21 0.035
667
c CHR692 Chronic Encephalitis 20 0.035
669
P LNG032 Lung Cancer 97 0.028
670
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.028
671
c FNC027 Fanconi Anemia, Complementation Group a 81 0.028
672
P LNG064 Lung Cancer Susceptibility 3 77 0.028
673
P PRK057 Parkinson Disease, Late-Onset 76 0.028
674
CRV035 Cervical Cancer 76 0.028
675
P SCH015 Schizophrenia 75 0.028
676
ADR007 Adrenoleukodystrophy 74 0.028
677
c HMC039 Hemochromatosis, Type 1 74 0.028
678
LPT014 Leptin Deficiency or Dysfunction 73 0.028
679
P FML011 Familial Adenomatous Polyposis 72 0.028
680
PRP027 Peripheral Vascular Disease 71 0.028
681
HMN044 Human Immunodeficiency Virus Type 1 71 0.028
682
WLS001 Wilson Disease 70 0.028
683
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.028
684
BHC003 Behcet Syndrome 70 0.028
685
c MGR028 Migraine with or Without Aura 1 69 0.028
686
RCK004 Rickets 69 0.028
687
P HYP086 Hypothyroidism 68 0.028
688
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.028
689
BRN024 Bronchitis 68 0.028
690
P INF038 Influenza 68 0.028
691
MST024 Mastocytosis, Cutaneous 67 0.028
692
P CHR012 Chronic Granulomatous Disease 67 0.028
693
ALL003 Allergic Rhinitis 67 0.028
694
SVR097 Severe Cutaneous Adverse Reaction 67 0.028
695
c FML001 Familial Atrial Fibrillation 66 0.028
696
OST159 Osteogenic Sarcoma 66 0.028
697
P DYS007 Dyskeratosis Congenita 66 0.028
698
P ATR011 Atrial Fibrillation 66 0.028
699
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.028
700
MRK001 Merkel Cell Carcinoma 66 0.028
701
ANG054 Angina Pectoris 66 0.028
702
P SHW006 Shwachman-Diamond Syndrome 1 66 0.028
703
P LNG028 Long Qt Syndrome 65 0.028
704
c SML038 Small Cell Cancer of the Lung 65 0.028
705
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.028
706
GST092 Gastroesophageal Reflux 65 0.028
707
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.028
708
c WLM013 Wilms Tumor 1 65 0.028
709
P EPD009 Epidermolysis Bullosa Dystrophica 64 0.028
710
P MTR014 Motor Neuron Disease 64 0.028
711
NRM005 Neuromuscular Disease 63 0.028
712
P GLM045 Glioma 63 0.028
713
KRN002 Kearns-Sayre Syndrome 63 0.028
714
PPL049 Papillon-Lefevre Syndrome 63 0.028
715
P END044 Endometriosis 62 0.028
716
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.028
717
P PRD008 Periodontitis 62 0.028
718
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.028
719
c WLM018 Wilms Tumor 5 62 0.028
720
TKY002 Takayasu Arteritis 61 0.028
721
INT002 Intermittent Claudication 61 0.028
722
P TST021 Testicular Germ Cell Tumor 61 0.028
723
P SNS001 Sensorineural Hearing Loss 61 0.028
724
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.028
725
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.028
726
P MYC008 Myocarditis 59 0.028
727
STT001 Status Epilepticus 59 0.028
728
P BRN022 Bronchiectasis 59 0.028
729
c SVR003 Severe Congenital Neutropenia 59 0.028
730
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.028
731
P PLY017 Polyarteritis Nodosa 58 0.028
732
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 58 0.028
733
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 57 0.028
734
GST033 Gestational Diabetes 57 0.028
735
PLY023 Polycystic Liver Disease 57 0.028
736
c CHL140 Chilblain Lupus 1 57 0.028
737
c ESS001 Essential Tremor 56 0.028
738
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 0.028
739
P FBR017 Fibrosarcoma 56 0.028
740
PGM001 Pigmented Villonodular Synovitis 56 0.028
741
P DYS193 Dystonia 11, Myoclonic 56 0.028
742
ALP097 Alopecia Universalis Congenita 56 0.028
743
c ACT075 Acute Myocardial Infarction 56 0.028
744
P OPT009 Optic Neuritis 56 0.028
745
DYS164 Dyskeratosis Congenita, X-Linked 56 0.028
746
P PLY011 Polycystic Ovary Syndrome 56 0.028
747
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 56 0.028
748
GST050 Gastrointestinal System Disease 56 0.028
749
P HYP024 Hypoparathyroidism 55 0.028
750
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 55 0.028
751
HYP691 Hypomelanosis of Ito 55 0.028
752
PLM010 Pulmonary Edema 55 0.028
753
c INT064 Intermediate Uveitis 55 0.028
754
P ANT006 Antiphospholipid Syndrome 54 0.028
755
CRY003 Cryptosporidiosis 54 0.028
756
RFL001 Reflex Sympathetic Dystrophy 53 0.028
757
HDR002 Hidradenitis Suppurativa 53 0.028
758
P LTR001 Lateral Sclerosis 53 0.028
759
MYM001 Myoma 53 0.028
760
SNS003 Sensory Peripheral Neuropathy 53 0.028
761
MMB001 Membranoproliferative Glomerulonephritis 53 0.028
762
GST023 Gastric Ulcer 53 0.028
763
c DMN023 Diamond-Blackfan Anemia 1 52 0.028
764
GLM004 Gliomatosis Cerebri 52 0.028
765
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.028
766
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.028
767
DSM007 Desmoplastic Small Round Cell Tumor 52 0.028
768
P HYP210 Hypomagnesemia 2, Renal 51 0.028
769
MCR141 Mucormycosis 51 0.028
770
CRY001 Cryptogenic Organizing Pneumonia 51 0.028
771
PLR008 Pleurisy 51 0.028
772
c SCN007 Secondary Hyperparathyroidism 50 0.028
773
c NTR049 Neutropenia, Severe Congenital, 3, Autosomal Recessive 50 0.028
774
WLL006 Wells Syndrome 50 0.028
775
c PSR021 Psoriasis 14, Pustular 49 0.028
776
c HNT004 Huntington Disease-Like 2 49 0.028
777
HDR003 Hidradenitis 49 0.028
778
GYN001 Gynecomastia 49 0.028
779
URM002 Uremia 49 0.028
780
BCT004 Bacteriuria 48 0.028
781
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 48 0.028
782
PRS012 Pars Planitis 48 0.028
783
SPR010 Sporotrichosis 48 0.028
784
CLC006 Calcinosis 48 0.028
785
P SCL015 Scleritis 48 0.028
786
FCL012 Facial Paralysis 48 0.028
787
NCR004 Nocardiosis 48 0.028
788
CMB081 Combined Immunodeficiency, X-Linked 48 0.028
789
STM006 Stomach Disease 48 0.028
790
P CRN028 Corneal Ulcer 47 0.028
791
GRM005 Germ Cell Cancer 47 0.028
792
PPL002 Papillary Carcinoma 47 0.028
793
c PRM093 Premature Ovarian Failure 7 47 0.028
794
P VTR007 Vitreoretinopathy 46 0.028
795
OPS006 Opsoclonus-Myoclonus Syndrome 46 0.028
796
CNG028 Congenital Hypoplastic Anemia 46 0.028
797
GST010 Gestational Trophoblastic Neoplasm 46 0.028
798
P TRN034 Transverse Myelitis 46 0.028
799
c INH020 Inherited Metabolic Disorder 46 0.028
800
LMB050 Limbal Stem Cell Deficiency 45 0.028
801
GLL048 Glial Tumor 45 0.028
802
P OCY003 Oocyte Maturation Defect 1 45 0.028
803
CLL014 Cll/sll 45 0.028
804
PGM003 Pigmentation Disease 44 0.028
805
CRB004 Cerebral Artery Occlusion 44 0.028
806
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.028
807
ATN004 Autonomic Neuropathy 44 0.028
808
P TST026 Testicular Germ Cell Cancer 44 0.028
809
c ATM099 Autoimmune Uveitis 44 0.028
810
PMP004 Pemphigus Foliaceus 43 0.028
811
CRS001 Crescentic Glomerulonephritis 43 0.028
812
DRG024 Drug Allergy 43 0.028
813
TST015 Testicular Disease 43 0.028
814
OVR112 Ovarian Germ Cell Cancer 43 0.028
815
BCK006 Back Pain 42 0.028
816
DFF003 Diffuse Scleroderma 42 0.028
817
ACT088 Acute Insulin Response 41 0.028
818
P DMY001 Demyelinating Polyneuropathy 41 0.028
819
PSD001 Pseudobulbar Palsy 40 0.028
820
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.028
821
P CRN026 Corneal Edema 40 0.028
822
KLD004 Keloid Disorder 40 0.028
823
TRC077 Trichomegaly 40 0.028
824
URM005 Uremic Pruritus 39 0.028
825
P 8P1002 8p11 Myeloproliferative Syndrome 39 0.028
826
P BCL005 B Cell Prolymphocytic Leukemia 39 0.028
827
ALG001 Algoneurodystrophy 39 0.028
828
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.028
829
EYL005 Eyelid Disease 38 0.028
830
TRP005 Trophoblastic Neoplasm 38 0.028
831
OVR094 Ovarian Epithelial Cancer 38 0.028
832
MRN002 Mooren's Ulcer 38 0.028
833
PPL019 Papillary Conjunctivitis 38 0.028
834
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.028
835
P CRB059 Cerebellar Degeneration 37 0.028
836
MLR007 Male Reproductive System Disease 36 0.028
837
RFR013 Refractory Celiac Disease 35 0.028
838
GRM010 Germ Cells Tumors 34 0.028
839
LTT002 Letterer-Siwe Disease 34 0.028
840
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.028
841
ADH001 Adhesions of Uterus 33 0.028
842
FTD001 Foot Drop 33 0.028
843
CND006 Candida Glabrata 32 0.028
844
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.028
845
P PLY188 Polyendocrinopathy 32 0.028
846
RDT001 Radiation Cystitis 32 0.028
847
ASH001 Asherman's Syndrome 32 0.028
848
NRD001 Neurodermatitis 32 0.028
849
ANN011 Annular Erythema 32 0.028
850
PRN033 Paraneoplastic Neurologic Disorders 31 0.028
851
INF021 Infant Gynecomastia 31 0.028
852
LCH014 Lichen Amyloidosis 31 0.028
853
PMP009 Pemphigus Erythematosus 31 0.028
854
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.028
855
LCH003 Lichen Nitidus 30 0.028
856
c TST046 Testicular Germ Cell Tumor 1 29 0.028
857
P SCK034 Sickle Beta Thalassemia 29 0.028
858
OCC001 Occupational Dermatitis 29 0.028
859
ERY066 Erythema Multiforme Major 28 0.028
860
PRN032 Paraneoplastic Cerebellar Degeneration 28 0.028
861
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 28 0.028
862
c JVN024 Juvenile Hereditary Hemochromatosis 26 0.028
863
BCL008 B-Cell Childhood Acute Lymphoblastic Leukemia 26 0.028
864
PTY004 Pityriasis Lichenoides 26 0.028
865
MLG164 Malignant Epithelial Tumor of Ovary 26 0.028
866
IMM053 Immunotactoid Glomerulopathy 26 0.028
867
FBR085 Fibrillary Glomerulonephritis 25 0.028
868
ESN022 Eosinophilic Colitis 25 0.028
869
CHL075 Cheilitis Glandularis 25 0.028
870
c DRM055 Dermatitis, Atopic, 3 25 0.028
871
P PPL026 Papular Mucinosis 24 0.028
872
UND004 Undetermined Colitis 24 0.028
873
JVN026 Jeavons Syndrome 24 0.028
874
IDP095 Idiopathic Steroid-Resistant Nephrotic Syndrome 23 0.028
875
CHR176 Chromophil Renal Cell Carcinoma 23 0.028
876
P C1Q005 C1q Nephropathy 22 0.028
877
PHL001 Phlyctenulosis 21 0.028
878
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 18 0.028
879
INF184 Infective Keratitis 17 0.028
880
GRN045 Granulosis Rubra Nasi 15 0.028
881
P OVR042 Ovarian Cancer 89 0.020
882
MLR004 Malaria 80 0.020
883
PFF001 Pfeiffer Syndrome 79 0.020
884
P LYN001 Lynch Syndrome 77 0.020
885
c TBR025 Tuberous Sclerosis 1 76 0.020
886
PHN003 Phenylketonuria 75 0.020
887
c MNN043 Meningioma, Familial 74 0.020
888
ACR006 Aceruloplasminemia 73 0.020
889
P ALG028 Alagille Syndrome 1 73 0.020
890
P FML018 Familial Mediterranean Fever 72 0.020
891
MSC157 Muscular Dystrophy, Duchenne Type 71 0.020
892
P MYC007 Myocardial Infarction 70 0.020
893
P TBR001 Tuberous Sclerosis 70 0.020
894
SMT004 Smith-Lemli-Opitz Syndrome 69 0.020
895
CRT072 Creutzfeldt-Jakob Disease 69 0.020
896
P OCL013 Oculodentodigital Dysplasia 69 0.020
897
NVS017 Nevus, Epidermal 68 0.020
898
P ALP004 Alport Syndrome 68 0.020
899
LYM007 Lymphangioleiomyomatosis 68 0.020
900
P CLC063 Celiac Disease 1 68 0.020
901
P MLG056 Malignant Hyperthermia 67 0.020
902
P CRD119 Cardiac Arrest 67 0.020
903
P TMP003 Temporal Arteritis 67 0.020
904
P DMN002 Dementia 67 0.020
905
CMM004 Common Variable Immunodeficiency 67 0.020
906
P LPR021 Leprosy 3 67 0.020
907
ALC007 Alcohol Dependence 66 0.020
908
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.020
909
P MSC005 Muscular Dystrophy 66 0.020
910
OMN001 Omenn Syndrome 66 0.020
911
P BRD002 Bardet-Biedl Syndrome 66 0.020
912
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.020
913
c PRD013 Periodic Fever, Familial, Autosomal Dominant 65 0.020
914
c HMP029 Hemophilia a 65 0.020
915
P HYD006 Hydrocephalus 65 0.020
916
P HRM001 Hermansky-Pudlak Syndrome 65 0.020
917
P ART005 Arteriovenous Malformation 65 0.020
918
RBR001 Roberts Syndrome 65 0.020
919
PRT036 Peritonitis 65 0.020
920
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.020
921
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.020
922
P CNG001 Congenital Myasthenic Syndrome 64 0.020
923
CLF027 Cleft Palate, Isolated 64 0.020
924
OST017 Osteomyelitis 64 0.020
925
NRF007 Neurofibroma 64 0.020
926
HYP020 Hyperprolactinemia 64 0.020
927
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.020
928
TTN003 Tetanus 64 0.020
929
IRR002 Irritable Bowel Syndrome 63 0.020
930
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.020
931
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.020
932
INC021 Incontinentia Pigmenti 63 0.020
933
ANR007 Anorexia Nervosa 63 0.020
934
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.020
935
c PRG047 Progressive Familial Intrahepatic Cholestasis 62 0.020
936
P ART023 Arthropathy 62 0.020
937
TRN015 Transient Cerebral Ischemia 62 0.020
938
MNN042 Meningioma, Radiation-Induced 62 0.020
939
PSR001 Psoriatic Arthritis 62 0.020
940
P ESP024 Esophagitis 62 0.020
941
P CRG003 Crigler-Najjar Syndrome, Type I 61 0.020
942
P MVM001 Movement Disease 61 0.020
943
CRC021 Carcinosarcoma 61 0.020
944
c BRN108 Branchiootic Syndrome 1 61 0.020
945
NRL005 Neurilemmoma 60 0.020
946
P OCL002 Oculocutaneous Albinism 60 0.020
947
RCT015 Reactive Arthritis 60 0.020
948
MCR013 Microphthalmia 60 0.020
949
ARG002 Argininosuccinic Aciduria 60 0.020
950
INS001 Insulinoma 60 0.020
951
STF001 Stiff-Person Syndrome 60 0.020
952
MRT001 Muir-Torre Syndrome 60 0.020
953
P SLP005 Sleep Disorder 59 0.020
954
P ECT006 Ectodermal Dysplasia 59 0.020
955
MXD005 Mixed Connective Tissue Disease 59 0.020
956
FBR086 Fibrolamellar Carcinoma 59 0.020
957
HRL003 Hurler Syndrome 59 0.020
958
VLV032 Vulva Cancer 59 0.020
959
ANT024 Anthrax Disease 58 0.020
960
CHL067 Cholecystitis 58 0.020
961
P NPH005 Nephronophthisis 58 0.020
962
P ALC033 Alcohol Use Disorder 58 0.020
963
BRS051 Breast Disease 58 0.020
964
P TYR004 Tyrosinemia 58 0.020
965
EXT034 Extrinsic Allergic Alveolitis 58 0.020
966
CST005 Castleman Disease 57 0.020
967
P MMP001 Mumps 57 0.020
968
CPR004 Coproporphyria, Hereditary 57 0.020
969
IRN002 Iron Metabolism Disease 57 0.020
970
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.020
971
P PRN023 Prion Disease 57 0.020
972
CHR003 Cherubism 57 0.020
973
APH002 Aphasia 57 0.020
974
PLC005 Placental Insufficiency 57 0.020
975
P PYL005 Pyelonephritis 56 0.020
976
SPN041 Spinal Cord Disease 56 0.020
977
P BPL003 Bipolar Disorder 56 0.020
978
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 56 0.020
979
P RST002 Restrictive Cardiomyopathy 56 0.020
980
c INT072 Intestinal Pseudo-Obstruction 56 0.020
981
ACS001 Acoustic Neuroma 56 0.020
982
EPD002 Epidermolytic Hyperkeratosis 56 0.020
983
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.020
984
CMM005 Common Cold 56 0.020
985
ALL006 Allergic Asthma 56 0.020
986
P PLM034 Pulmonary Emphysema 56 0.020
987
P GST044 Gastritis 55 0.020
988
SYN007 Synovitis 55 0.020
989
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.020
990
P BRT004 Bartter Disease 55 0.020
991
CHL014 Cholera 55 0.020
992
GNG005 Gangliocytoma 55 0.020
993
INT007 Intermediate Coronary Syndrome 55 0.020
994
P VNS003 Venous Insufficiency 55 0.020
995
P DBT005 Diabetes Insipidus 55 0.020
996
FCT001 Factor Viii Deficiency 55 0.020
997
DBT010 Diabetic Neuropathy 55 0.020
998
PRN038 Prune Belly Syndrome 55 0.020
999
AMN003 Amnestic Disorder 54 0.020
1000
HYP060 Hyperinsulinism 54 0.020
1001
P RST001 Restless Legs Syndrome 54 0.020
1002
ANL018 Analbuminemia 54 0.020
1003
FCL014 Focal Epilepsy 54 0.020
1004
HST011 Histoplasmosis 54 0.020
1005
PRC013 Pericarditis 54 0.020
1006
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.020
1007
PLM012 Pulmonary Sarcoidosis 53 0.020
1008
c ATM024 Autoimmune Pancreatitis 53 0.020
1009
RCS002 Recessive Dystrophic Epidermolysis Bullosa 53 0.020
1010
HMC014 Homocysteinemia 53 0.020
1011
P PRK001 Porokeratosis 53 0.020
1012
INT051 Intussusception 53 0.020
1013
P LCT002 Lactose Intolerance 53 0.020
1014
THR013 Thoracic Outlet Syndrome 53 0.020
1015
EXP004 Exophthalmos 52 0.020
1016
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.020
1017
OST011 Osteomalacia 52 0.020
1018
c GLL024 Gallbladder Disease 1 52 0.020
1019
P RTN022 Retinal Vein Occlusion 52 0.020
1020
NPH003 Nephrocalcinosis 51 0.020
1021
PTH003 Pathologic Nystagmus 51 0.020
1022
P HMP007 Hemophilia 51 0.020
1023
P PNV001 Panuveitis 51 0.020
1024
BLD053 Blood Platelet Disease 51 0.020
1025
c VRL007 Viral Encephalitis 51 0.020
1026
P LCT001 Lactic Acidosis 51 0.020
1027
NNL006 Non-Alcoholic Steatohepatitis 51 0.020
1028
P PRC012 Pericardial Effusion 51 0.020
1029
SCB001 Scabies 51 0.020
1030
RTN003 Retinal Ischemia 50 0.020
1031
ENT011 Enterocolitis 50 0.020
1032
BRN014 Bronchopneumonia 50 0.020
1033
P TMP001 Temporal Lobe Epilepsy 50 0.020
1034
PRT014 Protein S Deficiency 50 0.020
1035
CHR078 Chorioretinitis 50 0.020
1036
P MGR003 Migraine with Aura 50 0.020
1037
DYS015 Dysentery 50 0.020
1038
LPR001 Lepromatous Leprosy 50 0.020
1039
FSC004 Fasciitis 50 0.020
1040
HYP080 Hypogonadism 50 0.020
1041
CRN030 Coronary Stenosis 50 0.020
1042
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 50 0.020
1043
c VRL005 Viral Pneumonia 49 0.020
1044
P KRT007 Keratoconus 49 0.020
1045
NPH010 Nephrosclerosis 49 0.020
1046
c CNT016 Central Retinal Vein Occlusion 49 0.020
1047
CHL004 Cholelithiasis 49 0.020
1048
PLC008 Placenta Disease 49 0.020
1049
RNL011 Renal Osteodystrophy 49 0.020
1050
LRN003 Learning Disability 49 0.020
1051
EPD006 Epidermolysis Bullosa Acquisita 49 0.020
1052
P OPN001 Open-Angle Glaucoma 49 0.020
1053
c CHR431 Chronic Venous Insufficiency 49 0.020
1054
MNN009 Meningoencephalitis 49 0.020
1055
CRY004 Cryoglobulinemia 49 0.020
1056
HPT009 Hepatopulmonary Syndrome 49 0.020
1057
PPL021 Papilledema 48 0.020
1058
URT001 Urethritis 48 0.020
1059
c ACT150 Acute Adrenal Insufficiency 48 0.020
1060
VTM033 Vitamin K Deficiency Bleeding 48 0.020
1061
ASP007 Aspiration Pneumonia 48 0.020
1062
SXL003 Sexual Disorder 48 0.020
1063
FRN020 Frontal Fibrosing Alopecia 48 0.020
1064
SPL018 Splenomegaly 48 0.020
1065
DDN006 Duodenitis 48 0.020
1066
AST006 Astigmatism 47 0.020
1067
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 47 0.020
1068
SPN021 Spinal Meningioma 47 0.020
1069
c BCT013 Bacterial Pneumonia 47 0.020
1071
MDS022 Mediastinitis 47 0.020
1072
GLS007 Glossitis 47 0.020
1073
TNP001 Tinea Pedis 47 0.020
1074
CRD001 Cardiac Tamponade 46 0.020
1075
SRT004 Serotonin Syndrome 46 0.020
1076
P PLY020 Polyradiculoneuropathy 46 0.020
1077
STV007 Stevens-Johnson Syndrome/toxic Epidermal