Search results for mtor

1218 hits were found for mtor

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 97 3.625
2
SMT020 Smith-Kingsmore Syndrome 38 3.291
3
GLB015 Glioblastoma Multiforme 75 3.154
4
P LNG032 Lung Cancer 98 3.097
5
P CLR023 Colorectal Cancer 99 3.070
6
FCL081 Focal Cortical Dysplasia, Type Ii 58 3.068
7
P HPT023 Hepatocellular Carcinoma 100 2.889
8
P PNC035 Pancreatic Cancer 84 2.822
9
P OVR042 Ovarian Cancer 88 2.804
10
P PRS040 Prostate Cancer 97 2.776
11
END057 Endometrial Cancer 74 2.755
12
P TBR001 Tuberous Sclerosis 70 2.617
13
P KDN017 Kidney Cancer 60 2.542
14
P GST053 Gastric Cancer 83 2.525
15
RNL114 Renal Cell Carcinoma, Nonpapillary 78 2.506
16
HYP266 Hypoxia 57 2.452
17
P ALZ034 Alzheimer Disease 88 2.399
18
P MLN008 Melanoma 69 2.381
19
SRC014 Sarcoma 65 2.373
20
CRV035 Cervical Cancer 76 2.194
21
P KDN018 Kidney Disease 72 2.168
22
MSC007 Muscle Hypertrophy 64 2.143
23
RNL065 Renal Cell Carcinoma, Papillary, 1 73 2.115
24
P EPL164 Epilepsy 71 2.112
25
CLR030 Clear Cell Renal Cell Carcinoma 53 2.089
26
SBP001 Subependymal Giant Cell Astrocytoma 49 2.077
27
KPS004 Kaposi Sarcoma 75 2.073
28
ESP021 Esophageal Cancer 90 2.068
29
NRN004 Neuroendocrine Tumor 55 2.064
30
HMM003 Hemimegalencephaly 48 2.059
31
P HNT016 Huntington Disease 72 2.055
32
ANG018 Angiomyolipoma 46 2.045
33
LYM007 Lymphangioleiomyomatosis 69 2.041
34
c SYS001 Systemic Lupus Erythematosus 86 2.031
35
P DBT009 Diabetes Mellitus 64 1.990
36
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 1.970
37
ADN011 Adenoid Cystic Carcinoma 70 1.945
38
P PLY014 Polycystic Kidney Disease 62 1.825
39
P NRB001 Neuroblastoma 72 1.822
40
MNT001 Mantle Cell Lymphoma 69 1.799
41
P NSP012 Nasopharyngeal Carcinoma 66 1.786
42
STM007 Stomatitis 50 1.786
43
c TBR025 Tuberous Sclerosis 1 77 1.774
44
MCS002 Mucositis 56 1.771
45
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 1.764
46
P ATS364 Autism 70 1.760
47
P GLM040 Glioma Susceptibility 1 81 1.752
48
DFF005 Diffuse Large B-Cell Lymphoma 55 1.736
49
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.723
50
P MSC003 Muscular Atrophy 52 1.714
51
P RHB003 Rhabdomyosarcoma 63 1.709
52
P THY023 Thymoma 65 1.704
53
GST040 Gastric Adenocarcinoma 70 1.694
54
c TBR026 Tuberous Sclerosis 2 72 1.683
55
CYT008 Cytomegalovirus Infection 57 1.683
56
P RRB004 Rare Breast Tumor 43 1.678
57
NNL006 Non-Alcoholic Steatohepatitis 54 1.666
58
RRC011 Rare Cancer of Corpus Uteri 36 1.666
59
BLD131 Bladder Urothelial Carcinoma 62 1.660
60
P LYM033 Lymphoproliferative Syndrome 59 1.660
61
MYL005 Myelofibrosis 70 1.654
62
P LMY004 Leiomyosarcoma 63 1.654
63
P FRG001 Fragile X Syndrome 70 1.647
64
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.647
65
MCR004 Macroglobulinemia 49 1.640
66
c NRF023 Neurofibromatosis, Type Ii 80 1.633
67
P MDL005 Medulloblastoma 77 1.633
68
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.633
69
LGH007 Leigh Syndrome 70 1.633
70
P HMN010 Hemangioma 61 1.633
71
P SCH015 Schizophrenia 74 1.625
72
FCL014 Focal Epilepsy 54 1.625
73
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.617
74
P RTT002 Rett Syndrome 80 1.608
75
c CWD006 Cowden Syndrome 1 78 1.608
76
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 1.608
77
LNG039 Lung Squamous Cell Carcinoma 66 1.608
78
HMT002 Hematologic Cancer 62 1.608
79
END062 Endometrial Hyperplasia 48 1.608
80
P OVR106 Ovarian Clear Cell Carcinoma 44 1.608
81
CHR072 Chordoma 58 1.599
82
OVR034 Ovarian Clear Cell Adenocarcinoma 38 1.599
83
P RTN008 Retinitis Pigmentosa 79 1.588
84
P PRK057 Parkinson Disease, Late-Onset 78 1.588
85
P APL001 Aplastic Anemia 74 1.588
86
c BSL007 Basal Cell Carcinoma 68 1.588
87
DRM014 Dermatofibrosarcoma Protuberans 65 1.588
88
P SPN046 Spinal Muscular Atrophy 62 1.588
89
P BRS044 Breast Adenocarcinoma 59 1.588
90
PRN014 Paronychia 49 1.588
91
HYP025 Hyperphosphatemia 48 1.588
92
c HYP595 Hypertension, Essential 84 1.576
93
c EXD008 Exudative Vitreoretinopathy 1 71 1.576
94
ALX003 Alexander Disease 59 1.576
95
P INT070 Intestinal Obstruction 58 1.576
96
P LNG035 Lung Large Cell Carcinoma 54 1.576
97
P CRN025 Corneal Dystrophy 49 1.576
98
FBR012 Fabry Disease 72 1.562
99
P ANG001 Angelman Syndrome 69 1.562
100
c MCL013 Mucolipidosis Iv 66 1.562
101
ALV005 Alveolar Soft Part Sarcoma 61 1.562
102
P NPH005 Nephronophthisis 59 1.562
103
OCL006 Ocular Hypertension 53 1.562
104
c LRG001 Large Cell Carcinoma 50 1.562
105
P MCL001 Mucolipidosis 48 1.562
106
c LKM061 Leukemia, Acute Myeloid 84 1.416
107
P LNG064 Lung Cancer Susceptibility 3 78 1.393
108
MYL069 Myeloma, Multiple 85 1.380
109
P EXN002 Exanthem 57 1.293
110
CHL065 Cholangiocarcinoma 68 1.284
111
LYM143 Lymphoma, Non-Hodgkin, Familial 72 1.265
112
KDN015 Kidney Angiomyolipoma 45 1.221
113
BRT002 Birt-Hogg-Dube Syndrome 63 1.169
114
SPP011 Suppression of Tumorigenicity 12 59 1.169
115
P CYS039 Cystic Kidney Disease 54 1.169
116
P PRT008 Proteus Syndrome 64 1.160
117
KPS002 Kaposiform Hemangioendothelioma 43 1.160
118
P CWD010 Cowden Syndrome 67 1.137
119
PLS025 Plasmablastic Lymphoma 47 1.137
120
LYM005 Lymphocele 35 1.137
121
PLY023 Polycystic Liver Disease 57 1.123
122
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.123
123
LRY029 Laryngomalacia 47 1.123
124
HPT006 Hepatic Angiomyolipoma 32 1.123
125
CHL044 Childhood Kidney Angiomyolipoma 10 1.123
126
P BNG030 Benign Ependymoma 60 1.104
127
KRT071 Keratosis, Seborrheic 58 1.104
128
THY025 Thymus Cancer 58 1.104
129
P PRV006 Pervasive Developmental Disorder 57 1.104
130
CRT033 Corticobasal Degeneration 57 1.104
131
SPN041 Spinal Cord Disease 56 1.104
132
PLM135 Palmoplantar Keratoderma, Bothnian Type 51 1.104
133
UMB002 Umbilical Hernia 46 1.104
134
CRN285 Corneal Dystrophy, Fleck 42 1.104
135
HRT007 Heart Cancer 42 1.104
136
CRD118 Cardiovascular Cancer 41 1.104
137
SBP002 Subependymal Glioma 40 1.104
138
c MLG036 Malignant Spiradenoma 38 1.104
139
ACN010 Acanthoma 38 1.104
140
OVR015 Ovarian Mixed Germ Cell Neoplasm 35 1.104
141
ESP001 Esophageal Tuberculosis 34 1.104
142
DRM003 Dermatosis Papulosa Nigra 33 1.104
143
c EXD010 Exudative Vitreoretinopathy 6 31 1.104
144
KDN016 Kidney Benign Neoplasm 29 1.104
145
CNT109 Central Nervous System Benign Neoplasm 28 1.104
146
THY026 Thymus Gland Disease 28 1.104
147
c LRG002 Large Cell Acanthoma 26 1.104
148
c ATS009 Autosomal Genetic Disease 25 1.104
149
VLV039 Vulvar Seborrheic Keratosis 25 1.104
150
MLN005 Melanoacanthoma 21 1.104
151
CLL012 Cell Type Benign Neoplasm 21 1.104
152
P VGN018 Vaginal Carcinosarcoma 19 1.104
153
VGN012 Vaginal Adenosarcoma 19 1.104
154
P GLM045 Glioma 63 0.235
155
GLL048 Glial Tumor 45 0.232
156
P MYL006 Myeloid Leukemia 60 0.196
157
P BCL017 B-Cell Lymphoma 58 0.195
158
SQM006 Squamous Cell Carcinoma 60 0.193
159
c SML038 Small Cell Cancer of the Lung 65 0.185
160
P BLD134 Bladder Cancer 79 0.181
161
P LKM062 Leukemia, Acute Lymphoblastic 69 0.180
162
P LYM118 Lymphoma 68 0.178
163
P ADN016 Adenocarcinoma 64 0.175
164
THY029 Thyroid Carcinoma 59 0.175
165
OST159 Osteogenic Sarcoma 66 0.170
166
HYP066 Hyperglycemia 61 0.168
167
c MCR113 Microvascular Complications of Diabetes 3 52 0.159
168
c MCR120 Microvascular Complications of Diabetes 7 47 0.159
169
c MCR130 Microvascular Complications of Diabetes 6 41 0.159
170
c MCR133 Microvascular Complications of Diabetes 4 41 0.159
171
ATM095 Autoimmune Disease 62 0.152
172
c PCH010 Pachyonychia Congenita 3 44 0.151
173
c ATS007 Autism Spectrum Disorder 67 0.142
174
AGN016 Aging 56 0.142
175
P RTN024 Retinoblastoma 73 0.137
176
P LKM002 Leukemia 68 0.137
177
FTT001 Fatty Liver Disease 61 0.137
178
ISC004 Ischemia 58 0.137
179
c FML008 Familial Retinoblastoma 53 0.137
180
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.127
181
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.125
182
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.123
183
P AST007 Astrocytoma 51 0.121
184
LYM133 Lymphoma, Hodgkin, Classic 69 0.119
185
P NTR004 Neutropenia 63 0.119
186
P NRF002 Neurofibromatosis 56 0.119
187
ORL015 Oral Squamous Cell Carcinoma 43 0.119
188
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.117
189
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.117
190
SPN035 Spindle Cell Sarcoma 53 0.117
191
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.112
192
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.112
193
P OVR082 Overgrowth Syndrome 50 0.112
194
P SKN015 Skin Carcinoma 66 0.110
195
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.110
196
SPN186 Spinal Cord Injury 60 0.110
197
P SZR006 Seizure Disorder 56 0.110
198
INT079 Intrahepatic Cholangiocarcinoma 51 0.110
199
CRB004 Cerebral Artery Occlusion 45 0.110
200
SVR004 Severe Combined Immunodeficiency 73 0.108
201
P LVR013 Liver Disease 68 0.108
202
VSL002 Visual Epilepsy 59 0.108
203
c MLG068 Malignant Glioma 46 0.108
204
c LKM063 Leukemia, Chronic Myeloid 72 0.105
205
ADN018 Adenoma 59 0.105
206
INS024 Insulin-Like Growth Factor I 79 0.103
207
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.103
208
OST012 Osteoarthritis 78 0.100
209
DWN001 Down Syndrome 70 0.100
210
OVR094 Ovarian Epithelial Cancer 38 0.100
211
c THY107 Thymoma, Familial 52 0.098
212
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 36 0.098
213
P PLM036 Pulmonary Fibrosis 65 0.095
214
SKN016 Skin Disease 63 0.095
215
BRK010 Burkitt Lymphoma 67 0.093
216
ATH013 Atherosclerosis Susceptibility 65 0.093
217
P HYP750 Hypertriglyceridemia, Familial 62 0.093
218
LNG099 Lung Disease 60 0.093
219
STT001 Status Epilepticus 60 0.093
220
HYP060 Hyperinsulinism 54 0.093
221
END086 End Stage Renal Disease 51 0.093
222
LYM019 Lymphosarcoma 46 0.093
223
P MCR115 Microvascular Complications of Diabetes 5 66 0.090
224
ORL011 Oral Cancer 60 0.090
225
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.090
226
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.090
227
P MGL013 Megalencephaly 45 0.090
228
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.090
229
P GRF003 Graft-Versus-Host Disease 72 0.087
230
P END044 Endometriosis 63 0.087
231
GLC003 Glucose Intolerance 54 0.087
232
P TMP001 Temporal Lobe Epilepsy 50 0.087
233
BRN071 Brain Injury 49 0.087
235
c HYP836 Hypercholesterolemia, Familial, 1 73 0.084
236
P PSR002 Psoriasis 62 0.084
237
SFT003 Soft Tissue Sarcoma 56 0.084
238
PST011 Pustulosis of Palm and Sole 52 0.084
239
TLN003 Telangiectasis 52 0.084
240
RNL077 Renal Fibrosis 47 0.084
241
P CHR345 Chronic Pain 44 0.084
242
c HPT073 Hepatitis C Virus 72 0.081
243
SKN019 Skin Melanoma 68 0.081
244
P LPS004 Lupus Erythematosus 61 0.081
245
P ATX030 Ataxia-Telangiectasia 82 0.078
246
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.078
247
PTZ001 Peutz-Jeghers Syndrome 70 0.078
248
c CHR684 Chronic Kidney Disease 70 0.078
249
P THR014 Thrombocytopenia 67 0.078
250
DPR016 Depression 63 0.078
251
LPD008 Lipid Metabolism Disorder 62 0.078
252
MNT002 Mental Depression 58 0.078
253
P BNG032 Benign Mesothelioma 46 0.078
254
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.075
255
P LKM071 Leukemia, Chronic Lymphocytic 79 0.075
256
P MJR001 Major Depressive Disorder 68 0.075
257
P FLL037 Follicular Lymphoma 67 0.075
258
c PRC016 Pre-Eclampsia 63 0.075
259
CLT003 Colitis 62 0.075
260
INS001 Insulinoma 60 0.075
261
c ACT073 Acute Leukemia 58 0.075
262
P GLL018 Gallbladder Cancer 57 0.075
263
P CHN012 Chondrosarcoma 56 0.075
264
P LRY044 Larynx Cancer 55 0.075
265
P LTR001 Lateral Sclerosis 54 0.075
266
P SPP010 Suppressor of Tumorigenicity 3 51 0.075
267
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.075
268
c LKM005 Leukemia, T-Cell, Chronic 34 0.075
269
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.075
270
P PHC003 Pheochromocytoma 71 0.071
271
P PLM037 Pulmonary Hypertension 67 0.071
272
P VSC007 Vascular Disease 63 0.071
273
P PLY011 Polycystic Ovary Syndrome 56 0.071
274
TRN018 Transitional Cell Carcinoma 56 0.071
275
ADR040 Adrenal Gland Pheochromocytoma 46 0.071
276
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.071
277
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.071
278
P MYP004 Myopathy 70 0.067
279
EWN003 Ewing Sarcoma 69 0.067
280
P PRD008 Periodontitis 64 0.067
281
P ANP001 Anaplastic Large Cell Lymphoma 58 0.067
282
ISL001 Islet Cell Tumor 56 0.067
283
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.067
284
SPL018 Splenomegaly 48 0.067
285
NRN001 Neuroendocrine Carcinoma 47 0.067
286
CYT002 Cytokine Deficiency 42 0.067
287
ALL014 Allergic Encephalomyelitis 38 0.067
288
GST019 Gastrointestinal Stromal Tumor 78 0.064
289
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.064
290
c ATR087 Atrial Standstill 1 75 0.064
291
FCT007 Factor Vii Deficiency 67 0.064
292
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.064
293
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.064
294
LVR012 Liver Cirrhosis 62 0.064
295
P MYC008 Myocarditis 59 0.064
296
P ADL017 Adult T-Cell Leukemia 56 0.064
297
HPT022 Hepatoblastoma 56 0.064
298
P DRR001 Diarrhea 55 0.064
299
P PTT006 Pituitary Adenoma 55 0.064
300
LNG031 Lung Benign Neoplasm 51 0.064
301
P VTR007 Vitreoretinopathy 46 0.064
302
PTT037 Pituitary Tumors 44 0.064
303
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.064
304
OVR063 Overnutrition 44 0.064
305
PRV003 Perivascular Epithelioid Cell Tumor 37 0.064
306
c PRS136 Prostate Cancer, Hereditary, 6 33 0.064
307
c PRS130 Prostate Cancer, Hereditary, 8 32 0.064
308
BRN028 Brain Cancer 74 0.059
309
c MNN043 Meningioma, Familial 74 0.059
310
PNC129 Pancreatic Adenocarcinoma 68 0.059
311
MYC006 Mycosis Fungoides 66 0.059
312
P MSC005 Muscular Dystrophy 66 0.059
313
CLN015 Colon Adenocarcinoma 65 0.059
314
c HPT001 Hepatitis C 62 0.059
315
c SVR001 Severe Acute Respiratory Syndrome 62 0.059
316
MNN042 Meningioma, Radiation-Induced 62 0.059
317
WLD007 Waldenstroem's Macroglobulinemia 61 0.059
318
P FBR017 Fibrosarcoma 56 0.059
319
PST046 Post-Transplant Lymphoproliferative Disease 53 0.059
320
P RTN016 Retinal Degeneration 53 0.059
321
P RTN018 Retinal Disease 53 0.059
322
CLR109 Colorectal Adenocarcinoma 51 0.059
323
TRM010 Traumatic Brain Injury 51 0.059
324
SPN021 Spinal Meningioma 50 0.059
325
c PRM038 Primary Agammaglobulinemia 44 0.059
326
c MLG079 Malignant Pleural Mesothelioma 42 0.059
327
SCR001 Secretory Meningioma 41 0.059
328
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.059
330
P RHM011 Rheumatoid Arthritis 80 0.055
331
c NRF024 Neurofibromatosis, Type I 77 0.055
332
ULC004 Ulcerative Colitis 73 0.055
333
P SRC025 Sarcoidosis 1 70 0.055
334
MYL009 Myelodysplastic Syndrome 70 0.055
335
ART016 Aortic Aneurysm 69 0.055
336
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.055
337
HYP056 Hypoglycemia 66 0.055
338
MYL031 Myeloproliferative Neoplasm 66 0.055
339
MRK001 Merkel Cell Carcinoma 65 0.055
340
ACT119 Acute Promyelocytic Leukemia 63 0.055
341
ALL026 Allergic Hypersensitivity Disease 62 0.055
342
c SCL052 Scleroderma, Familial Progressive 61 0.055
343
WST001 West Syndrome 61 0.055
344
P ENC018 Encephalopathy 61 0.055
345
P BND020 Bone Disease 59 0.055
346
LYM027 Lymphopenia 58 0.055
347
VSC002 Vascular Dementia 57 0.055
348
c ACT134 Acute Liver Failure 56 0.055
349
P MTC069 Mitochondrial Disorders 56 0.055
350
P NRP001 Neuropathy 56 0.055
351
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.055
352
P INF037 Inflammatory Bowel Disease 54 0.055
353
LYM040 Lymphoblastic Lymphoma 54 0.055
354
PPL022 Papilloma 54 0.055
355
PLS009 Plasma Cell Neoplasm 51 0.055
356
HYP017 Hypophosphatemia 50 0.055
357
P CTN015 Cutaneous T Cell Lymphoma 49 0.055
358
ADR016 Adrenal Cortical Carcinoma 48 0.055
359
BNR002 Bone Resorption Disease 48 0.055
360
LYM012 Lymphoplasmacytic Lymphoma 47 0.055
361
SQM002 Squamous Cell Papilloma 46 0.055
362
URT010 Ureteral Obstruction 45 0.055
364
P RRT020 Rare Tumor 41 0.055
365
ADR004 Adrenal Cortical Adenocarcinoma 39 0.055
366
PRM329 Premature Aging 35 0.055
367
HMN016 Hemangioendothelioma 34 0.055
369
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.050
370
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.050
371
P MYC007 Myocardial Infarction 70 0.050
372
THY111 Thyroid Carcinoma, Familial Medullary 67 0.050
373
c RHB024 Rhabdomyosarcoma 2 67 0.050
374
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.050
375
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.050
376
ANG020 Angiosarcoma 64 0.050
377
NRM005 Neuromuscular Disease 64 0.050
378
NRF007 Neurofibroma 64 0.050
379
CLR108 Colorectal Adenoma 64 0.050
380
TXC005 Toxic Shock Syndrome 62 0.050
381
CHL068 Cholestasis 61 0.050
382
GST033 Gestational Diabetes 61 0.050
383
NRL005 Neurilemmoma 60 0.050
384
INT066 Interstitial Lung Disease 60 0.050
385
c ACT027 Acute Pancreatitis 60 0.050
386
SRC027 Sarcoma, Synovial 58 0.050
387
P GLM007 Glomerulonephritis 57 0.050
388
CST005 Castleman Disease 57 0.050
389
P FCL005 Focal Segmental Glomerulosclerosis 57 0.050
390
PLS011 Plasmacytoma 56 0.050
391
BRN004 Brain Edema 56 0.050
392
P GST044 Gastritis 56 0.050
393
CRC006 Carcinoid Syndrome 55 0.050
394
GNG004 Ganglioglioma 54 0.050
395
LYM022 Lymphangioma 54 0.050
396
P LCH002 Lichen Planus 53 0.050
397
FNG017 Fungal Infectious Disease 53 0.050
398
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.050
399
P RCT021 Rectum Cancer 52 0.050
400
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.050
401
c HRD202 Hereditary Lymphedema I 50 0.050
402
THY125 Thyroid Gland Medullary Carcinoma 50 0.050
403
DGN001 Degenerative Disc Disease 48 0.050
404
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.050
405
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.050
406
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.050
407
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.050
408
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.050
409
ORL013 Oral Lichen Planus 45 0.050
410
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.050
411
CRT015 Carotid Artery Occlusion 45 0.050
412
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.050
413
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.050
414
CVD001 Covid-19 44 0.050
415
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.050
416
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.050
417
MSN004 Mesenchymal Cell Neoplasm 41 0.050
418
P MLG074 Malignant Mesenchymoma 40 0.050
419
ANX004 Anoxia 40 0.050
420
GLM044 Glomerular Disease 37 0.050
421
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 36 0.050
422
PLY150 Polykaryocytosis Inducer 31 0.050
423
P RSP003 Respiratory Failure 74 0.045
424
CRH001 Crohn's Disease 74 0.045
425
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.045
426
P ASP006 Aspergillosis 69 0.045
427
PLY001 Polycythemia Vera 69 0.045
428
P SYS005 Systemic Scleroderma 68 0.045
429
RCK004 Rickets 68 0.045
430
P HPT021 Hepatitis 67 0.045
431
P OLG002 Oligodendroglioma 67 0.045
432
CRB039 Cerebrovascular Disease 67 0.045
433
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.045
434
P HYD006 Hydrocephalus 66 0.045
435
P LPS002 Liposarcoma 65 0.045
436
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.045
437
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.045
438
P HML002 Hemolytic Anemia 63 0.045
439
END041 Endometrial Adenocarcinoma 63 0.045
440
PSR001 Psoriatic Arthritis 61 0.045
441
OST003 Osteonecrosis 61 0.045
442
RTN017 Retinal Detachment 61 0.045
443
SZR001 Sezary's Disease 60 0.045
444
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.045
445
PRT013 Portal Hypertension 59 0.045
446
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.045
447
P MLN069 Melanoma, Uveal 59 0.045
448
P DNG005 Dengue Virus 59 0.045
449
PST028 Post-Traumatic Stress Disorder 58 0.045
450
P PRP019 Peripheral Nervous System Disease 58 0.045
451
P INF032 Infertility 57 0.045
452
P UVT001 Uveitis 57 0.045
453
P RHN004 Rhinitis 57 0.045
454
P PRN023 Prion Disease 57 0.045
455
P PLY018 Polycythemia 56 0.045
456
P ANT006 Antiphospholipid Syndrome 55 0.045
457
P ART021 Arteriosclerosis 54 0.045
458
DBT010 Diabetic Neuropathy 54 0.045
459
PNC001 Pancytopenia 54 0.045
460
P INS002 in Situ Carcinoma 53 0.045
461
MST005 Mastitis 53 0.045
462
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.045
463
MRG003 Marginal Zone B-Cell Lymphoma 52 0.045
464
DSM007 Desmoplastic Small Round Cell Tumor 52 0.045
465
c ACT135 Acute Graft Versus Host Disease 52 0.045
466
LMY002 Leiomyoma 52 0.045
467
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.045
468
47X002 47,xyy 49 0.045
469
c FLL041 Follicular Lymphoma 1 49 0.045
470
MTC005 Mitochondrial Metabolism Disease 49 0.045
471
ACT084 Acute Stress Disorder 47 0.045
472
LYM009 Lymphocytic Choriomeningitis 47 0.045
473
MLT113 Multicentric Castleman Disease 47 0.045
474
GST071 Gastrointestinal Carcinoma 47 0.045
475
PLY100 Polyploidy 40 0.045
476
48X005 48,xyyy 39 0.045
477
P PRP021 Peripheral Nervous System Neoplasm 39 0.045
479
BRN053 Bronchial Adenomas/carcinoids Childhood 25 0.045
480
c FNC027 Fanconi Anemia, Complementation Group a 81 0.039
481
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.039
482
MSC157 Muscular Dystrophy, Duchenne Type 72 0.039
483
P FML011 Familial Adenomatous Polyposis 72 0.039
484
DFC004 Deficiency Anemia 70 0.039
485
c GLY008 Glycogen Storage Disease Ii 70 0.039
486
P HYP061 Hypertrophic Cardiomyopathy 70 0.039
487
ADL002 Adult Syndrome 70 0.039
488
P PNM007 Pneumonia 68 0.039
489
P INF038 Influenza 68 0.039
490
P FRN006 Frontotemporal Dementia 68 0.039
491
P CRD119 Cardiac Arrest 67 0.039
492
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.039
493
c MCR129 Microvascular Complications of Diabetes 1 66 0.039
494
PRT037 Pertussis 65 0.039
495
P HRP006 Herpes Simplex 65 0.039
496
PRT036 Peritonitis 64 0.039
497
LSH001 Leishmaniasis 63 0.039
498
c MLG084 Malignant Fibrous Histiocytoma 63 0.039
499
TRN015 Transient Cerebral Ischemia 63 0.039
500
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.039
501
MDD011 Mood Disorder 62 0.039
502
VRL011 Viral Infectious Disease 61 0.039
503
P NPH012 Nephrotic Syndrome 60 0.039
504
P MCR010 Microcephaly 59 0.039
505
GRD007 Grade Iii Astrocytoma 59 0.039
506
P ALC033 Alcohol Use Disorder 58 0.039
507
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 58 0.039
508
EYD002 Eye Disease 58 0.039
509
CRV038 Cervical Squamous Cell Carcinoma 58 0.039
510
P BNC003 Bone Cancer 58 0.039
511
P CND004 Candidiasis 58 0.039
512
c CHR417 Chronic Graft Versus Host Disease 57 0.039
513
P PLY041 Polymyositis 57 0.039
514
c MST023 Mesothelioma, Malignant 57 0.039
515
CMR002 Coumarin Resistance 56 0.039
516
P PNL012 Penile Cancer 56 0.039
517
P MLN007 Male Infertility 55 0.039
518
PRS045 Prostatic Hypertrophy 53 0.039
519
P MNC007 Monocytic Leukemia 53 0.039
520
P CNT005 Central Nervous System Lymphoma 53 0.039
521
ERD001 Erdheim-Chester Disease 53 0.039
522
DMY004 Demyelinating Disease 52 0.039
523
P PRG013 Paraganglioma 52 0.039
524
LYS002 Lysosomal Storage Disease 52 0.039
525
IMP005 Impotence 52 0.039
526
FDL002 Food Allergy 51 0.039
527
P LCT001 Lactic Acidosis 51 0.039
528
TNG007 Tongue Carcinoma 51 0.039
529
SKN013 Skin Benign Neoplasm 51 0.039
530
P SCK005 Sickle Cell Disease 50 0.039
531
CLR003 Clear Cell Adenocarcinoma 50 0.039
532
GST049 Gastrointestinal System Cancer 49 0.039
533
URM002 Uremia 49 0.039
534
VCC001 Vaccinia 49 0.039
535
c PRM226 Primary Central Nervous System Lymphoma 48 0.039
536
P HMN032 Human Herpesvirus 8 47 0.039
537
RTC005 Reticulosarcoma 47 0.039
538
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.039
539
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.039
540
P OVR046 Ovarian Cyst 47 0.039
541
RTN023 Retinitis 46 0.039
542
RTN020 Retinal Vascular Disease 46 0.039
543
P LPM005 Lipomatosis 46 0.039
544
P MGL030 Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 46 0.039
545
PLY012 Polyhydramnios 46 0.039
546
END031 Endometrial Stromal Sarcoma 46 0.039
547
LTH001 Lethal Midline Granuloma 44 0.039
548
ACN001 Acinar Cell Carcinoma 44 0.039
549
CLP005 Ciliopathy 43 0.039
550
SMN007 Seminoma 43 0.039
551
NRF003 Neurofibrosarcoma 43 0.039
552
P HYP265 Hypotonia 43 0.039
553
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.039
554
NRR001 Neuroretinitis 42 0.039
555
P KLZ004 Kala-Azar 1 41 0.039
556
c MCR112 Microvascular Complications of Diabetes 2 41 0.039
557
PLY062 Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy 40 0.039
558
KLD004 Keloid Disorder 40 0.039
559
TRC005 Tracheal Stenosis 38 0.039
560
HRW001 Hair Whorl 36 0.039
561
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.039
562
c CHR064 Chronic Monocytic Leukemia 33 0.039
563
P RRL003 Rare Lymphatic Malformation 31 0.039
564
CLR137 Clear Cell Adenocarcinoma of the Ovary 31 0.039
565
MLG163 Malignant Tumor of Penis 29 0.039
566
HDG004 Hodgkin's Granuloma 23 0.039
567
HDG006 Hodgkin's Paragranuloma 22 0.039
568
MLR004 Malaria 81 0.032
569
CYS001 Cystic Fibrosis 81 0.032
570
STR067 Stroke, Ischemic 81 0.032
571
c DLT002 Dilated Cardiomyopathy 79 0.032
572
P HRT032 Heart Disease 75 0.032
573
P OST002 Osteoporosis 74 0.032
574
ANX010 Anxiety 73 0.032
575
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.032
576
P MLT020 Multiple Sclerosis 72 0.032
577
PRP027 Peripheral Vascular Disease 71 0.032
578
CNG034 Congestive Heart Failure 69 0.032
579
P DMN001 Diamond-Blackfan Anemia 69 0.032
580
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.032
581
P SLP006 Sleep Apnea 69 0.032
582
P MYC084 Mycobacterium Tuberculosis 1 68 0.032
583
c NMN015 Niemann-Pick Disease, Type C1 68 0.032
584
P MYS003 Myasthenia Gravis 68 0.032
585
P ESS003 Essential Thrombocythemia 68 0.032
586
BRN024 Bronchitis 68 0.032
587
CNN005 Connective Tissue Disease 68 0.032
588
HYL004 Hyaline Fibromatosis Syndrome 67 0.032
589
P SHW006 Shwachman-Diamond Syndrome 1 67 0.032
590
FLL027 Fallopian Tube Carcinoma 67 0.032
591
P HYP098 Hypereosinophilic Syndrome 67 0.032
592
P DRM053 Dermatitis, Atopic 66 0.032
593
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.032
594
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.032
595
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.032
596
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.032
597
OVR029 Ovarian Hyperstimulation Syndrome 64 0.032
598
CLF027 Cleft Palate, Isolated 64 0.032
599
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.032
600
P GCH001 Gaucher's Disease 63 0.032
601
P PTT014 Pitt-Hopkins Syndrome 63 0.032
602
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.032
603
RHB001 Rhabdoid Cancer 63 0.032
604
c FNC043 Fanconi Anemia, Complementation Group E 62 0.032
605
NNN026 Noonan Syndrome with Multiple Lentigines 62 0.032
606
LPP008 Lipoprotein Quantitative Trait Locus 62 0.032
607
P VSC011 Vasculitis 62 0.032
608
DRM006 Dermatitis 61 0.032
609
c WLM018 Wilms Tumor 5 61 0.032
610
P PNC044 Pancreatitis 61 0.032
611
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.032
612
P SCL018 Scoliosis 60 0.032
613
ACQ007 Acquired Immunodeficiency Syndrome 60 0.032
614
c ORF037 Orofaciodigital Syndrome I 60 0.032
615
CHC001 Chickenpox 60 0.032
616
P CTR002 Cataract 60 0.032
617
c ACT071 Acute Kidney Failure 60 0.032
618
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.032
619
DCT002 Ductal Carcinoma in Situ 59 0.032
620
P CYS018 Cystitis 59 0.032
621
AVN001 Avian Influenza 59 0.032
622
P NMN002 Niemann-Pick Disease 59 0.032
623
CYS010 Cystinosis 59 0.032
624
P PLY006 Polydactyly 59 0.032
625
PPT005 Peptic Ulcer Disease 59 0.032
626
BRS051 Breast Disease 58 0.032
627
CNS004 Constipation 58 0.032
628
c DWL002 Dowling-Degos Disease 1 58 0.032
629
GLS018 Glass Syndrome 57 0.032
630
CHL067 Cholecystitis 57 0.032
631
IRN002 Iron Metabolism Disease 57 0.032
632
CHK001 Chikungunya 57 0.032
633
THY122 Thyroid Gland Cancer 57 0.032
634
c ACT075 Acute Myocardial Infarction 57 0.032
635
THR024 Thrombosis 57 0.032
636
BLR008 Bilirubin Metabolic Disorder 57 0.032
637
c LKM070 Leukemia, Acute Monocytic 57 0.032
638
ALL006 Allergic Asthma 56 0.032
639
LMY014 Leiomyoma, Uterine 56 0.032
640
BCT022 Bacterial Infectious Disease 56 0.032
641
ANS011 Anus Cancer 56 0.032
642
ACS001 Acoustic Neuroma 56 0.032
643
MTH009 Mouth Disease 56 0.032
644
EMB004 Embryonal Carcinoma 56 0.032
645
GST050 Gastrointestinal System Disease 56 0.032
646
MCL006 Macular Retinal Edema 55 0.032
647
ZLL002 Zollinger-Ellison Syndrome 55 0.032
648
VSC003 Visceral Leishmaniasis 55 0.032
649
ANG005 Anogenital Venereal Wart 55 0.032
650
HDR002 Hidradenitis Suppurativa 55 0.032
651
JVN009 Juvenile Pilocytic Astrocytoma 55 0.032
652
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.032
653
GST037 Gastroparesis 54 0.032
654
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.032
655
HMS001 Hemosiderosis 54 0.032
656
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 53 0.032
657
MMM001 Mammary Paget's Disease 53 0.032
658
PRP036 Peripheral T-Cell Lymphoma 53 0.032
659
P ORL007 Oral Cavity Cancer 53 0.032
660
c HPT007 Hepatitis E 53 0.032
661
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.032
662
PLM014 Pleomorphic Adenoma 52 0.032
663
ACR041 Acromelic Frontonasal Dysostosis 52 0.032
664
SMT003 Somatostatinoma 52 0.032
665
ART140 Arteries, Anomalies of 52 0.032
666
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 52 0.032
667
P NRC002 Narcolepsy 52 0.032
668
ACT200 Acute Monoblastic Leukemia 52 0.032
669
DFF036 Differentiated Thyroid Carcinoma 52 0.032
670
P BRN035 Brain Stem Glioma 52 0.032
671
SRS001 Serous Cystadenocarcinoma 52 0.032
672
SPN051 Spondylitis 51 0.032
673
THR004 Thrombocytosis 51 0.032
675
PRS021 Prostatic Adenoma 51 0.032
676
VSC006 Vascular Cancer 51 0.032
677
SPL004 Splenic Marginal Zone Lymphoma 51 0.032
678
HND002 Hand, Foot and Mouth Disease 51 0.032
679
PTT041 Pituitary Stalk Interruption Syndrome 50 0.032
680
PST021 Postpartum Depression 50 0.032
681
CHR635 Chromosome 5q Deletion Syndrome 50 0.032
682
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.032
683
c INF145 Infantile Liver Failure Syndrome 1 50 0.032
684
MCP006 Mucoepidermoid Carcinoma 50 0.032
685
OCL022 Ocular Melanoma 50 0.032
686
c INF023 Inflammatory Breast Carcinoma 50 0.032
687
VRR004 Verrucous Carcinoma 49 0.032
688
P MTC133 Mitochondrial Myopathy 49 0.032
689
PLY024 Polymicrogyria 49 0.032
690
HDR003 Hidradenitis 49 0.032
691
PRS129 Prostatic Hyperplasia, Benign 49 0.032
692
LRN003 Learning Disability 49 0.032
693
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.032
694
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.032
695
IGG001 Iga Glomerulonephritis 48 0.032
696
HLX001 Helix Syndrome 47 0.032
697
CRC014 Carcinoid Tumors, Intestinal 47 0.032
698
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.032
699
SRT004 Serotonin Syndrome 47 0.032
700
ANV001 Anovulation 47 0.032
701
CNT033 Central Nervous System Cancer 47 0.032
702
TST044 Testicular Torsion 47 0.032
703
CHR074 Choriocarcinoma 47 0.032
704
AML029 Ameloblastoma 46 0.032
705
LPD009 Lipid Storage Disease 46 0.032
706
MCS004 Mucosal Melanoma 46 0.032
707
OBS004 Obstructive Hydrocephalus 46 0.032
708
GST030 Gastrinoma 45 0.032
709
MXD026 Mixed Glioma 45 0.032
710
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.032
711
LYM051 Lymphomatoid Granulomatosis 45 0.032
712
GLC036 Glucagonoma 45 0.032
713
BRN032 Brain Glioma 45 0.032
714
P EPT012 Epithelioid Sarcoma 44 0.032
715
TNG009 Tongue Squamous Cell Carcinoma 44 0.032
716
PRT035 Peritoneum Cancer 44 0.032
717
PPL001 Papillary Adenoma 44 0.032
718
ANL017 Anal Squamous Cell Carcinoma 44 0.032
719
LRG014 Large Cell Neuroendocrine Carcinoma 44 0.032
720
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.032
721
MDD018 Middle East Respiratory Syndrome 43 0.032
722
BLR013 Biliary Tract Cancer 42 0.032
723
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.032
724
P EPL196 Epilepsy, Familial Focal, with Variable Foci 1 41 0.032
725
P RRH023 Rare Hereditary Hemochromatosis 41 0.032
726
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.032
727
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.032
728
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 40 0.032
729
P MCR364 Macrodactyly 40 0.032
730
CHL045 Choline Deficiency Disease 39 0.032
731
PNC008 Pancreatic Endocrine Carcinoma 39 0.032
732
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.032
733
c MLG157 Malignant Pheochromocytoma 38 0.032
734
ANG065 Angioma, Tufted 38 0.032
735
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.032
736
DBT081 Diabetic Encephalopathy 37 0.032
737
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 37 0.032
738
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.032
739
TST043 Testicular Seminoma 35 0.032
740
CHR178 Chromosomal Triplication 35 0.032
741
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.032
742
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.032
743
PPL050 Papillary Tumor of the Pineal Region 33 0.032
744
INF009 Inflammatory Spondylopathy 31 0.032
745
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.032
746
c CLB022 Coloboma, Ocular, Autosomal Recessive 28 0.032
747
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.032
748
PLY179 Polyomavirus-Associated Nephropathy 24 0.032
749
EPD052 Epidermolysis Bullosa Simplex Superficialis 24 0.032
750
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.032
751
PST047 Post-Traumatic Epilepsy 22 0.032
752
HML018 Homologous Wasting Disease 22 0.032
753
RRS010 Rare Soft Tissue Tumor 18 0.032
754
P LYN001 Lynch Syndrome 77 0.022
755
P NNN008 Noonan Syndrome 1 76 0.022
756
P NJM001 Nijmegen Breakage Syndrome 74 0.022
757
VNH007 Von Hippel-Lindau Syndrome 73 0.022
758
c SPN225 Spondyloarthropathy 1 73 0.022
759
BSL036 Basal Cell Nevus Syndrome 73 0.022
760
P FML018 Familial Mediterranean Fever 73 0.022
761
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.022
762
HMN044 Human Immunodeficiency Virus Type 1 71 0.022
763
WLS001 Wilson Disease 71 0.022
764
P AMY004 Amyloidosis 70 0.022
765
MLT157 Multiple System Atrophy 1 70 0.022
766
c GCH015 Gaucher Disease, Type I 70 0.022
767
P OST001 Osteopetrosis 70 0.022
768
WRN001 Werner Syndrome 69 0.022
769
P ART022 Arthritis 69 0.022
770
CRB037 Cerebral Palsy 69 0.022
771
P LPR021 Leprosy 3 69 0.022
772
P MPL001 Maple Syrup Urine Disease 69 0.022
773
P CRN037 Craniosynostosis 68 0.022
774
CST001 Costello Syndrome 68 0.022
775
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.022
776
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.022
777
P DYS007 Dyskeratosis Congenita 67 0.022
778
c HMP029 Hemophilia a 67 0.022
779
PSY004 Psychotic Disorder 67 0.022
780
P TRN020 Turner Syndrome 67 0.022
781
c MGR028 Migraine with or Without Aura 1 67 0.022
782
ALC007 Alcohol Dependence 66 0.022
783
ANG054 Angina Pectoris 66 0.022
784
MYX005 Myxoid Liposarcoma 66 0.022
785
c FML346 Familial Adenomatous Polyposis 1 66 0.022
786
AND002 Androgen Insensitivity Syndrome 66 0.022
787
P ATR011 Atrial Fibrillation 66 0.022
788
CHG001 Chagas Disease 66 0.022
789
P BRD002 Bardet-Biedl Syndrome 66 0.022
790
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.022
791
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.022
792
P ART005 Arteriovenous Malformation 65 0.022
793
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.022
794
P MTR014 Motor Neuron Disease 65 0.022
795
BRR014 Barrett Esophagus 65 0.022
796
P CLD001 Cleidocranial Dysplasia 65 0.022
797
c WLM013 Wilms Tumor 1 65 0.022
798
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.022
799
MYC079 Myoclonic Epilepsy of Lafora 64 0.022
800
GT001 Gout 64 0.022
801
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.022
802
BRC012 Brucellosis 64 0.022
803
DGR001 Digeorge Syndrome 64 0.022
804
DSM004 Desmoid Tumor 64 0.022
805
HYP020 Hyperprolactinemia 64 0.022
806
P CRN300 Coronary Heart Disease 1 63 0.022
807
c ACT068 Acute Cystitis 63 0.022
808
c ATM011 Autoimmune Hepatitis 63 0.022
809
BDD001 Budd-Chiari Syndrome 63 0.022
810
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.022
811
ERL001 Early Myoclonic Encephalopathy 62 0.022
812
c HPT003 Hepatitis a 62 0.022
813
c BRN108 Branchiootic Syndrome 1 62 0.022
814
TKY002 Takayasu Arteritis 62 0.022
815
P ESP024 Esophagitis 62 0.022
816
c ANM038 Anemia, Autoimmune Hemolytic 62 0.022
817
BRS099 Breast Ductal Carcinoma 62 0.022
818
CTN007 Cutaneous Leishmaniasis 62 0.022
819
NTR005 Nutritional Deficiency Disease 62 0.022
820
P CRN038 Carney Complex Variant 61 0.022
821
ATY005 Atypical Teratoid Rhabdoid Tumor 61 0.022
822
P DRM010 Dermatomyositis 61 0.022
823
P INT143 Interstitial Cystitis 61 0.022
824
ALC006 Alcoholic Hepatitis 61 0.022
825
P SJG008 Sjogren Syndrome 61 0.022
826
APP008 Appendicitis 61 0.022
827
WLL001 Williams-Beuren Syndrome 60 0.022
828
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.022
829
P TST021 Testicular Germ Cell Tumor 60 0.022
830
CRD223 Cardiac Arrhythmia 60 0.022
831
P EMR001 Emery-Dreifuss Muscular Dystrophy 60 0.022
832
P GLY013 Glycogen Storage Disease 60 0.022
833
P THL005 Thalassemia 60 0.022
834
VGN017 Vaginal Cancer 60 0.022
835
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.022
836
P OPT006 Optic Nerve Disease 60 0.022
837
c HPT016 Hepatitis B 59 0.022
838
c PCH015 Pachyonychia Congenita 1 59 0.022
839
P SLP005 Sleep Disorder 59 0.022
840
P PRD006 Prader-Willi Syndrome 59 0.022
841
c HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 59 0.022
842
DNN001 Danon Disease 59 0.022
843
P GLL022 Guillain-Barre Syndrome 59 0.022
844
GST045 Gastroenteritis 59 0.022
845
HLC007 Helicobacter Pylori Infection 59 0.022
846
ANR040 Aneurysm 59 0.022
847
INC002 Inclusion Body Myositis 58 0.022
848
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.022
849
P SYP003 Syphilis 58 0.022
850
ANT024 Anthrax Disease 58 0.022
851
RBS001 Rabies 58 0.022
852
ERY029 Erythermalgia, Primary 58 0.022
853
CRD132 Cardiac Conduction Defect 58 0.022
854
c PRG018 Paragangliomas 1 58 0.022
855
ADR005 Adrenal Carcinoma 58 0.022
856
PMP006 Pemphigus Vulgaris, Familial 57 0.022
857
MCR013 Microphthalmia 57 0.022
858
BRN056 Bronchopulmonary Dysplasia 57 0.022
859
P SLV026 Salivary Gland Carcinoma 57 0.022
860
LYM021 Lymphadenitis 57 0.022
861
APH001 Aphthous Stomatitis 57 0.022
862
THY022 Thymic Carcinoma 57 0.022
863
TNS005 Tonsillitis 57 0.022
864
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.022
865
P CRD246 Cardiovascular System Disease 57 0.022
866
P FTL001 Fetal Alcohol Syndrome 57 0.022
867
SCH014 Schistosomiasis 57 0.022
868
SKN022 Skin Squamous Cell Carcinoma 57 0.022
869
P ANG015 Angioedema 57 0.022
870
P BPL003 Bipolar Disorder 56 0.022
871
P PYL005 Pyelonephritis 56 0.022
872
PNM008 Pneumothorax 56 0.022
873
P MYS005 Myositis 56 0.022
874
c LSS005 Lissencephaly 1 56 0.022
875
ADN027 Adenomyosis 56 0.022
876
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.022
877
HMG005 Hemoglobinopathy 56 0.022
878
c NPH055 Nephrotic Syndrome, Type 1 56 0.022
879
c FML035 Familial Hyperlipidemia 55 0.022
880
HST011 Histoplasmosis 55 0.022
881
HYP005 Hypokalemia 55 0.022
882
ORP003 Oropharynx Cancer 55 0.022
883
ORL004 Oral Submucous Fibrosis 55 0.022
884
LMB062 Limb Ischemia 55 0.022
885
P GRV001 Graves' Disease 55 0.022
886
CHR100 Chronic Ulcer of Skin 55 0.022
887
GNG005 Gangliocytoma 55 0.022
888
P HYP076 Hyperthyroidism 55 0.022
889
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.022
890
P VNS003 Venous Insufficiency 55 0.022
891
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.022
892
INT007 Intermediate Coronary Syndrome 55 0.022
893
GNT003 Genital Herpes 54 0.022
894
P SPN052 Spondyloarthropathy 54 0.022
895
PRP030 Purpura 54 0.022
896
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.022
897
P PMP001 Pemphigus 54 0.022
898
c FNC029 Fanconi Anemia, Complementation Group I 54 0.022
899
P MRN003 Marinesco-Sjogren Syndrome 54 0.022
900
SCH071 Schaaf-Yang Syndrome 54 0.022
901
VGN023 Vaginitis 54 0.022
902
P ALP008 Alopecia 54 0.022
903
PRT038 Protein-Energy Malnutrition 54 0.022
904
TND005 Tendinitis 54 0.022
905
PLM010 Pulmonary Edema 54 0.022
906
PSD007 Pseudomyxoma Peritonei 54 0.022
907
WST005 West Nile Virus 54 0.022
908
P FML012 Familial Partial Lipodystrophy 54 0.022
909
P TRM003 Tremor 54 0.022
910
P TCD001 Tic Disorder 53 0.022
911
P RNL017 Renal Oncocytoma 53 0.022
912
P HYP083 Hypopituitarism 53 0.022
913
P HML001 Hemolytic-Uremic Syndrome 53 0.022
914
P SHR001 Short Bowel Syndrome 53 0.022
915
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.022
916
HMC014 Homocysteinemia 53 0.022
917
OCL008 Oculopharyngeal Muscular Dystrophy 53 0.022
918
P FBR031 Febrile Seizures 53 0.022
919
GST023 Gastric Ulcer 53 0.022
920
DNT012 Dental Caries 53 0.022
921
INT051 Intussusception 53 0.022
922
P INT068 Intestinal Disease 53 0.022
923
EXP004 Exophthalmos 52 0.022
924
GNG002 Ganglioneuroma 52 0.022
925
CLB010 Coloboma of Macula 52 0.022
926
c VRL010 Viral Hepatitis 52 0.022
927
MGL038 Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome 52 0.022
928
NRT004 Neuritis 52 0.022
929
PLS007 Plasmodium Falciparum Malaria 52 0.022
930
P THY032 Thyroiditis 52 0.022
931
P PRV002 Periventricular Nodular Heterotopia 52 0.022
932
P OVR049 Ovarian Disease 52 0.022
933
THR009 Thrombocytopenia-Absent Radius Syndrome 52 0.022
934
INV006 Inverted Papilloma 52 0.022
935
P HMP007 Hemophilia 51 0.022
936
NPH003 Nephrocalcinosis 51 0.022
937
OCL069 Ocular Motor Apraxia 51 0.022
938
c NMN014 Niemann-Pick Disease, Type C2 51 0.022
939
MTP034 Metaphyseal Chondrodysplasia, Jansen Type 51 0.022
940
P MND003 Mandibuloacral Dysplasia with Type a Lipodystrophy 51 0.022
941
P LSS002 Lissencephaly 51 0.022
942
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.022
943
FBR008 Fibrillary Astrocytoma 51 0.022
944
c VRL007 Viral Encephalitis 51 0.022
945
TLR001 Tularemia 51 0.022
946
P HYP040 Hypospadias 51 0.022
947
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 51 0.022
948
PNN001 Panniculitis 51 0.022
949
CRV040 Cervix Carcinoma 51 0.022
950
P CHL066 Cholangitis 51 0.022
951
P MMB011 Membranous Nephropathy 50 0.022
952
LNT004 Lentigines 50 0.022
953
P FNC004 Fanconi Syndrome 50 0.022
954
RDC002 Radiculopathy 50 0.022
955
RTN003 Retinal Ischemia 50 0.022
956
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.022
957
HPT014 Hepatorenal Syndrome 50 0.022
958
FSC004 Fasciitis 50 0.022
959
PRT018 Portal Vein Thrombosis 50 0.022
960
P PNV001 Panuveitis 50 0.022
961
NTR046 Neutrophil Migration 50 0.022
962
MTB004 Metabolic Acidosis 50 0.022
963
P PNB001 Pineoblastoma 50 0.022
964
HYP080 Hypogonadism 50 0.022
965
P ATR005 Atrophic Gastritis 50 0.022
966
ONC007 Oncocytoma 49 0.022
967
P MYT002 Myotonic Dystrophy 49 0.022
968
ENT004 Enthesopathy 49 0.022
969
PPL021 Papilledema 49 0.022
970
P CRV039 Cervicitis 49 0.022
971
c CHR431 Chronic Venous Insufficiency 49 0.022
972
MCN001 Mucinous Adenocarcinoma 49 0.022
973
ERY004 Erysipelas 49 0.022
974
VRC001 Varicocele 49 0.022
975
ART017 Aortic Disease 49 0.022
976
SLD003 Sialadenitis 49 0.022
977
PLM041 Pulmonary Valve Stenosis 49 0.022
978
P CRV031 Cervical Adenocarcinoma 49 0.022
979
FRN020 Frontal Fibrosing Alopecia 49 0.022
980
HST010 Histiocytosis 48 0.022
981
DDF001 Dedifferentiated Liposarcoma 48 0.022
982
HYP043 Hyperandrogenism 48 0.022
983
INT017 Intestinal Schistosomiasis 48 0.022
984
WTH001 Withdrawal Disorder 48 0.022
985
ATS010 Autosomal Recessive Disease 48 0.022
986
CHR563 Chronic Eosinophilic Leukemia 48 0.022
987
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.022
988
c NPH049 Nephrotic Syndrome, Type 2 48 0.022
989
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.022
990
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.022
991
INT067 Interstitial Nephritis 48 0.022
992
DBT006 Diabetic Macular Edema 48 0.022
993
GNG008 Ganglioneuroblastoma 48 0.022
994
BLD044 Bladder Disease 48 0.022
995
GLC106 Glucocorticoid Resistance, Generalized 48 0.022
996
CYS002 Cystic Lymphangioma 48 0.022
997
c MTR002 Mitral Valve Insufficiency 48 0.022
998
DSM003 Desmoid Disease, Hereditary 48 0.022
999
CHL056 Cheilitis 48 0.022
1000
FBR009 Fibrous Dysplasia 48 0.022
1001
c CRD179 Ceroid Lipofuscinosis, Neuronal, 7 48 0.022
1002
PTT008 Pituitary Carcinoma 48 0.022
1003
ESN015 Eosinophilic Fasciitis 48 0.022
1004
MLK006 Milk Allergy 48 0.022
1005
P KRT005 Keratoacanthoma 48 0.022
1006
c HYD064 Hydrocephalus, Congenital, 1 48 0.022
1007
ART004 Aortic Atherosclerosis 47 0.022
1008
c PRM031 Primary Autosomal Recessive Microcephaly 47 0.022
1009
ADN009 Adenosquamous Carcinoma 47 0.022
1010
MCR018 Microcytic Anemia 47 0.022
1011
ASB001 Asbestosis 47 0.022
1012
PPL002 Papillary Carcinoma 47 0.022
1013
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.022
1014
THY128 Thyroid Tumor 47 0.022
1015
CRN027 Corneal Neovascularization 47 0.022
1016
c CNG216 Congenital Hydrocephalus 47 0.022
1017
PHS021 Phosphoglycerate Dehydrogenase Deficiency 47 0.022
1018
P PRC019 Precocious Puberty 46 0.022
1019
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.022
1020
c ACT076 Acute Myocarditis 46 0.022
1021
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.022
1022
TST014 Testicular Cancer 46 0.022
1023
c SCH079 Schizophrenia 1 46 0.022
1024
BRL010 Buruli Ulcer 46 0.022
1025
CWP001 Cowpox 46 0.022
1026
c DRR009 Diarrhea 6 46 0.022
1027
c ACT042 Acute Pyelonephritis 46 0.022
1028
BNS007 Bone Sarcoma 45 0.022
1029
INT253 Intestinal Benign Neoplasm 45 0.022
1030
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.022
1031
PNC056 Pineocytoma 45 0.022
1032
ACT003 Acute Kidney Tubular Necrosis 45 0.022
1033
NNS002 Nonspecific Interstitial Pneumonia 45 0.022
1034
URT051 Ureter, Cancer of 45 0.022
1035
CLL014 Cll/sll 45 0.022
1036
c SPR009 Sporadic Breast Cancer 45 0.022
1037
LRN001 Laurence-Moon Syndrome 45 0.022
1038
MYF001 Myofibroma 45 0.022
1039
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.022
1040
SBC016 Subacute Delirium 44 0.022
1041
DBT008 Diabetic Angiopathy 44 0.022
1042
APP009 Appendix Adenocarcinoma 44 0.022
1043
CRD043 Ceroid Storage Disease 44 0.022
1044
P MTC004 Mitochondrial Encephalomyopathy 44 0.022
1045
DWR001 Dwarfism 44 0.022
1046
P PRL003 Proliferative Glomerulonephritis 44 0.022
1047
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.022
1048
PLX002 Plexiform Neurofibroma 44 0.022
1049
MCR096 Macrocephaly/autism Syndrome 44 0.022
1050
P BNG095 Benign Giant Cell Tumor 44 0.022
1051
BCT021 Bacterial Sepsis 44 0.022
1052
MCR017 Macrocytic Anemia 44 0.022
1053
FBR054 Fibroma 44 0.022
1054
c ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 44 0.022
1055
END085 Endometrial Serous Adenocarcinoma 44 0.022
1056
ANP009 Anaplastic Oligodendroglioma 43 0.022
1057
CHN010 Chondroma 43 0.022
1058
TND004 Tendinopathy 43 0.022
1059
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.022
1060
P TST026 Testicular Germ Cell Cancer 43 0.022
1061
P HYP078 Hypertrophy of Breast 43 0.022
1062
CRB016 Carbuncle 43 0.022
1063
TST015 Testicular Disease 43 0.022
1064
URT037 Urethral Stricture 43 0.022
1065
GLL017 Gallbladder Adenocarcinoma 43 0.022
1066
ECC004 Eccrine Porocarcinoma 43 0.022
1067
NSP002 Nasopharyngitis 43 0.022
1068
DNT001 Dental Fluorosis 43 0.022
1069
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.022
1070
PRS036 Parasitic Protozoa Infectious Disease 43 0.022
1071
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 43 0.022
1072
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.022
1073
HYP457 Hypertrophic Scars 42 0.022
1074
TRP009 Triple X Syndrome 42 0.022
1075
P AVS003 Avascular Necrosis 42 0.022
1076
PRG014 Progesterone Resistance 42 0.022
1077
TRC097 Tracheomalacia 42 0.022
1078
ALC010 Alcoholic Cardiomyopathy 42 0.022
1079
LRY017 Laryngeal Disease 42 0.022
1080
EXC002 Exocrine Pancreatic Insufficiency 42 0.022
1081
ATX019 Ataxia with Vitamin E Deficiency 42 0.022
1082
c RTN041 Retinitis Pigmentosa 11 42 0.022
1083
OBS082 Obstructive Nephropathy 42 0.022
1084
c VTL009