Search results for Tetrahydrofolyl-[Glu](2)

10324 hits were found for Tetrahydrofolyl-[Glu](2)

# Family MCID Name MIFTS Score
1
P DBT009 Diabetes Mellitus 64 185.079
2
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 140.247
3
HYP056 Hypoglycemia 66 123.371
4
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 115.204
5
P HRP006 Herpes Simplex 65 94.249
6
HYP066 Hyperglycemia 61 93.773
7
c MCR113 Microvascular Complications of Diabetes 3 52 83.488
8
c MCR120 Microvascular Complications of Diabetes 7 47 83.183
9
c MCR133 Microvascular Complications of Diabetes 4 41 82.878
10
c MCR130 Microvascular Complications of Diabetes 6 41 82.860
11
LPD008 Lipid Metabolism Disorder 62 75.393
12
P MCR115 Microvascular Complications of Diabetes 5 66 74.357
13
P KDN018 Kidney Disease 72 74.317
14
P NRP001 Neuropathy 56 68.379
15
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 58.143
16
c CHR684 Chronic Kidney Disease 70 57.264
17
P BRS047 Breast Cancer 97 57.082
18
FTT001 Fatty Liver Disease 61 56.951
19
P VSC007 Vascular Disease 63 56.741
20
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 55.973
21
P CRN300 Coronary Heart Disease 1 63 55.249
22
LPP008 Lipoprotein Quantitative Trait Locus 62 54.706
23
P LNG032 Lung Cancer 98 54.679
24
P LVR013 Liver Disease 68 54.597
25
P NRF002 Neurofibromatosis 56 54.433
26
P HYP724 Hyperlipoproteinemia, Type Iii 73 52.904
27
P PRP019 Peripheral Nervous System Disease 58 52.819
28
RPD005 Rapidly Involuting Congenital Hemangioma 38 52.791
29
P LYM118 Lymphoma 68 52.536
30
END086 End Stage Renal Disease 51 52.508
31
48X005 48,xyyy 39 51.329
32
ART140 Arteries, Anomalies of 52 51.271
33
NNL005 Non-Alcoholic Fatty Liver Disease 61 51.155
34
DWN001 Down Syndrome 70 51.067
35
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 50.774
36
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 50.715
37
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 50.686
38
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 50.686
39
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 50.657
40
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 50.657
41
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 50.657
42
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 50.657
43
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 50.627
44
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 50.627
45
HMN044 Human Immunodeficiency Virus Type 1 71 50.213
46
P CLR023 Colorectal Cancer 99 50.153
47
c HYP595 Hypertension, Essential 84 49.765
48
P DRR001 Diarrhea 55 49.645
49
ATH013 Atherosclerosis Susceptibility 65 49.464
50
GLC003 Glucose Intolerance 54 49.010
51
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 48.674
52
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 48.181
53
ISC004 Ischemia 58 47.777
54
ADL002 Adult Syndrome 70 47.243
55
P PRD008 Periodontitis 64 47.243
56
P LKM002 Leukemia 68 47.180
57
HYP060 Hyperinsulinism 54 47.148
58
HRW001 Hair Whorl 36 46.958
59
P ADN016 Adenocarcinoma 64 46.799
60
c PRM038 Primary Agammaglobulinemia 44 46.671
61
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 46.318
62
P HRT032 Heart Disease 75 45.865
63
CNG034 Congestive Heart Failure 69 45.735
64
IMM167 Immune Deficiency Disease 78 45.538
65
P TRN020 Turner Syndrome 67 45.341
66
c SML038 Small Cell Cancer of the Lung 65 45.011
67
c HPT073 Hepatitis C Virus 72 44.712
68
P NTR004 Neutropenia 63 44.712
69
CYT002 Cytokine Deficiency 42 44.444
70
P NRB001 Neuroblastoma 72 43.802
71
P DNG005 Dengue Virus 59 43.734
72
PRP027 Peripheral Vascular Disease 71 43.391
73
P ALZ034 Alzheimer Disease 88 43.219
74
c RHB024 Rhabdomyosarcoma 2 67 42.942
75
PRT037 Pertussis 65 42.872
76
HLX001 Helix Syndrome 47 42.382
77
P OVR042 Ovarian Cancer 88 42.206
78
P HPT023 Hepatocellular Carcinoma 100 42.029
79
P MYL006 Myeloid Leukemia 60 42.029
80
P CRD246 Cardiovascular System Disease 57 41.851
81
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 41.780
82
CRB039 Cerebrovascular Disease 67 41.744
83
P TRC086 Trichohepatoenteric Syndrome 1 62 41.744
84
P PRS040 Prostate Cancer 97 41.672
85
ATM095 Autoimmune Disease 62 41.313
86
GST033 Gestational Diabetes 61 41.240
87
P PNC035 Pancreatic Cancer 84 41.059
88
RNL114 Renal Cell Carcinoma, Nonpapillary 78 41.059
89
c HYP836 Hypercholesterolemia, Familial, 1 73 39.730
90
ACN002 Acanthosis Nigricans 60 39.730
91
P MYC007 Myocardial Infarction 70 39.692
92
c MCR129 Microvascular Complications of Diabetes 1 66 39.692
93
DRM006 Dermatitis 61 39.504
94
c SVR001 Severe Acute Respiratory Syndrome 62 39.352
95
P HPT021 Hepatitis 67 39.200
96
SQM006 Squamous Cell Carcinoma 60 39.086
97
P GLM045 Glioma 63 39.010
98
P BCL017 B-Cell Lymphoma 58 38.933
99
P CTR002 Cataract 60 38.895
100
c HPT001 Hepatitis C 62 38.856
101
THR013 Thoracic Outlet Syndrome 54 38.818
102
ADN018 Adenoma 59 38.702
103
c AMY091 Amyotrophic Lateral Sclerosis 1 89 38.393
104
MYL069 Myeloma, Multiple 85 38.354
105
GLL048 Glial Tumor 45 38.276
106
LNG099 Lung Disease 60 38.198
107
THY029 Thyroid Carcinoma 59 38.081
108
RCK004 Rickets 68 37.963
109
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 37.766
110
ANR007 Anorexia Nervosa 63 37.726
111
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 37.726
112
c LKM061 Leukemia, Acute Myeloid 84 37.687
113
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 37.528
114
PLM129 Pulmonary Disease, Chronic Obstructive 73 37.449
115
LYM019 Lymphosarcoma 46 37.449
116
GLB015 Glioblastoma Multiforme 75 37.369
117
DPR016 Depression 63 37.088
118
LVR012 Liver Cirrhosis 62 37.088
119
P ANR048 Aniridia 1 63 36.887
120
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 36.724
121
P HYP750 Hypertriglyceridemia, Familial 62 36.521
122
P BLD134 Bladder Cancer 79 36.110
123
c SPN225 Spondyloarthropathy 1 73 36.069
124
DBT010 Diabetic Neuropathy 54 36.027
125
P MLN008 Melanoma 69 35.944
126
ATX010 Ataxia Neuropathy Spectrum 34 35.778
127
P HYP086 Hypothyroidism 69 35.736
128
ACT064 Acute Necrotizing Encephalitis 33 35.736
129
BLD137 Blood Group--Ahonen 16 35.736
130
P DRM053 Dermatitis, Atopic 66 35.653
131
P GST053 Gastric Cancer 83 35.232
132
OST012 Osteoarthritis 78 35.189
133
ACQ007 Acquired Immunodeficiency Syndrome 60 35.062
134
GNT003 Genital Herpes 54 35.019
135
DFC004 Deficiency Anemia 70 34.934
136
STR067 Stroke, Ischemic 81 34.848
137
LYM133 Lymphoma, Hodgkin, Classic 69 34.806
138
ALL026 Allergic Hypersensitivity Disease 62 34.720
139
c MCR112 Microvascular Complications of Diabetes 2 41 34.677
140
c NRF023 Neurofibromatosis, Type Ii 80 34.634
141
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 34.504
142
P PSR002 Psoriasis 62 34.374
143
47X002 47,xyy 49 34.374
144
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 34.113
145
ATN004 Autonomic Neuropathy 45 34.069
146
ANR040 Aneurysm 59 33.849
147
PST011 Pustulosis of Palm and Sole 52 33.805
148
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 33.628
149
TLN003 Telangiectasis 52 33.628
150
c DBT099 Diabetes Mellitus, Type I 65 33.450
151
NNL006 Non-Alcoholic Steatohepatitis 54 33.272
152
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 33.182
153
MNT002 Mental Depression 58 33.137
154
NTR005 Nutritional Deficiency Disease 62 33.047
155
PNG002 Pain Agnosia 51 33.001
156
P RHM011 Rheumatoid Arthritis 80 32.820
157
ATX019 Ataxia with Vitamin E Deficiency 42 32.820
158
c SYS001 Systemic Lupus Erythematosus 86 32.775
159
P MLT074 Multiple Endocrine Neoplasia 56 32.638
160
P MNN013 Meningitis 66 32.546
161
P MYP004 Myopathy 70 32.454
162
P EXN002 Exanthem 57 32.408
163
CRV035 Cervical Cancer 76 32.362
164
LNG031 Lung Benign Neoplasm 51 32.362
165
c PLM127 Pulmonary Hypertension, Primary, 3 34 32.224
166
AST005 Asthma 76 32.177
167
OST159 Osteogenic Sarcoma 66 32.177
168
P ENC004 Encephalitis 61 32.177
169
NRL005 Neurilemmoma 60 32.085
170
P SLP006 Sleep Apnea 69 32.038
171
P OST002 Osteoporosis 74 31.804
172
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 31.757
173
SRC014 Sarcoma 65 31.474
174
SPN035 Spindle Cell Sarcoma 53 31.427
175
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 31.284
176
P ART022 Arthritis 69 31.189
177
IMP005 Impotence 52 31.189
178
P ANG001 Angelman Syndrome 69 31.141
179
BNR002 Bone Resorption Disease 48 30.948
180
P PLY019 Polyneuropathy 56 30.900
181
P PHC003 Pheochromocytoma 71 30.803
182
c PRD040 Periodontitis, Chronic 53 30.803
184
TTN003 Tetanus 65 30.755
185
HYP266 Hypoxia 57 30.755
186
c ACT027 Acute Pancreatitis 60 30.706
187
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 30.706
188
ANX010 Anxiety 73 30.658
189
AND002 Androgen Insensitivity Syndrome 66 30.658
190
c ACT068 Acute Cystitis 63 30.658
191
c SPN301 Spinocerebellar Ataxia 2 58 30.658
192
MYL009 Myelodysplastic Syndrome 70 30.609
193
P SZR006 Seizure Disorder 56 30.609
194
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 30.609
195
c MLN055 Melanoma, Cutaneous Malignant 10 52 30.511
196
CVD001 Covid-19 44 30.463
197
P AXN002 Axenfeld-Rieger Syndrome 59 30.266
198
P LKM071 Leukemia, Chronic Lymphocytic 79 30.217
199
P MSC005 Muscular Dystrophy 66 30.118
200
P LKM062 Leukemia, Acute Lymphoblastic 69 30.068
201
ALR002 Al-Raqad Syndrome 33 30.019
202
P THR014 Thrombocytopenia 67 29.969
203
PLM031 Poliomyelitis 64 29.969
204
c ATR087 Atrial Standstill 1 75 29.919
205
P AMY004 Amyloidosis 70 29.919
206
ADR040 Adrenal Gland Pheochromocytoma 46 29.919
207
P INF037 Inflammatory Bowel Disease 54 29.819
208
P ATX030 Ataxia-Telangiectasia 82 29.719
209
DPH001 Diphtheria 60 29.517
210
P RHN004 Rhinitis 57 29.467
211
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 29.416
212
DBT084 Diabetes Mellitus, Ketosis-Prone 60 29.365
213
CNS004 Constipation 58 29.264
214
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 29.213
215
AGN016 Aging 56 29.213
216
P HYP098 Hypereosinophilic Syndrome 67 29.161
217
c HPT003 Hepatitis a 62 29.059
218
P LPS004 Lupus Erythematosus 61 29.059
219
c ACT075 Acute Myocardial Infarction 57 29.059
220
VSL002 Visual Epilepsy 59 28.904
221
LPT014 Leptin Deficiency or Dysfunction 74 28.801
222
ALC007 Alcohol Dependence 66 28.801
223
c BRN108 Branchiootic Syndrome 1 62 28.801
224
CRH001 Crohn's Disease 74 28.749
225
SKN016 Skin Disease 63 28.749
226
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 28.697
227
LYM143 Lymphoma, Non-Hodgkin, Familial 72 28.645
228
P RSP003 Respiratory Failure 74 28.541
229
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 28.541
230
END057 Endometrial Cancer 74 28.489
231
P PLM037 Pulmonary Hypertension 67 28.489
232
P GLM007 Glomerulonephritis 57 28.278
233
OCL069 Ocular Motor Apraxia 51 28.120
234
P KDN017 Kidney Cancer 60 28.066
235
P MYT002 Myotonic Dystrophy 49 27.960
236
HPT082 Hepatic Adenomas, Familial 44 27.853
237
ADP007 Adie Pupil 39 27.853
238
CHR178 Chromosomal Triplication 35 27.853
239
CYS001 Cystic Fibrosis 81 27.799
240
HNM002 Hinman Syndrome 27 27.799
241
PLM001 Pulmonary Tuberculosis 69 27.746
242
HMN014 Human Immunodeficiency Virus Infectious Disease 55 27.746
243
c CRV002 Cervix Uteri Carcinoma in Situ 46 27.746
244
CRV045 Cervical Intraepithelial Neoplasia 39 27.746
245
CHL123 Chlamydia 59 27.584
246
ULC004 Ulcerative Colitis 73 27.476
247
P THL005 Thalassemia 60 27.476
248
P ENC018 Encephalopathy 61 27.367
249
P PNM007 Pneumonia 68 27.257
250
P PLY011 Polycystic Ovary Syndrome 56 27.257
251
ANG054 Angina Pectoris 66 27.203
252
P INF038 Influenza 68 27.148
253
c PNS012 Paine Syndrome 61 27.148
254
P PRK057 Parkinson Disease, Late-Onset 78 27.093
255
BCT022 Bacterial Infectious Disease 56 27.093
256
c HPT016 Hepatitis B 59 27.038
257
c EPS039 Episodic Pain Syndrome, Familial, 1 42 27.038
258
P HYP069 Hyperparathyroidism 63 26.982
259
INT323 Intraocular Pressure Quantitative Trait Locus 62 26.816
260
c PRS136 Prostate Cancer, Hereditary, 6 33 26.816
261
c PRS130 Prostate Cancer, Hereditary, 8 32 26.816
262
P MTR004 Maturity-Onset Diabetes of the Young 65 26.705
263
c PRC016 Pre-Eclampsia 63 26.705
264
P PNC044 Pancreatitis 61 26.649
265
IRN002 Iron Metabolism Disease 57 26.649
266
P DMN002 Dementia 66 26.593
267
CLT003 Colitis 62 26.593
268
P PLM036 Pulmonary Fibrosis 65 26.424
269
HYP080 Hypogonadism 50 26.367
270
EYD002 Eye Disease 58 26.254
271
MCL006 Macular Retinal Edema 55 26.254
272
BRN071 Brain Injury 49 26.254
273
HNS001 Hansen's Disease 34 26.254
274
P SRC025 Sarcoidosis 1 70 26.140
275
P MJR001 Major Depressive Disorder 68 26.140
276
c ACT071 Acute Kidney Failure 60 26.083
277
P ALP008 Alopecia 54 25.968
278
P VSC011 Vasculitis 62 25.911
279
CHC001 Chickenpox 60 25.911
280
MNN042 Meningioma, Radiation-Induced 62 25.853
281
THR024 Thrombosis 57 25.853
282
PRP080 Peripheral Artery Disease 53 25.853
283
ATS010 Autosomal Recessive Disease 48 25.853
284
ART001 Arterial Tortuosity Syndrome 66 25.795
285
P LPR021 Leprosy 3 69 25.737
286
P INF032 Infertility 57 25.679
287
P OPN001 Open-Angle Glaucoma 49 25.679
288
ESP021 Esophageal Cancer 90 25.621
289
c MNN043 Meningioma, Familial 74 25.621
290
c FNC043 Fanconi Anemia, Complementation Group E 62 25.621
291
ALL003 Allergic Rhinitis 67 25.563
292
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 25.563
293
P LNG064 Lung Cancer Susceptibility 3 78 25.504
294
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 25.504
295
VCC001 Vaccinia 49 25.504
296
SVR004 Severe Combined Immunodeficiency 73 25.446
297
c THR092 Thrombophilia Due to Thrombin Defect 73 25.446
298
SKN019 Skin Melanoma 68 25.446
299
TXC005 Toxic Shock Syndrome 62 25.446
300
P SCL018 Scoliosis 60 25.446
301
PPL022 Papilloma 54 25.387
302
P ALP106 Alport Syndrome 1, X-Linked 55 25.269
303
c MGR028 Migraine with or Without Aura 1 67 25.151
304
DFF005 Diffuse Large B-Cell Lymphoma 55 25.151
305
SPN021 Spinal Meningioma 50 25.151
306
c DNT047 Dentinogenesis Imperfecta Type 2 31 25.151
307
P CRD119 Cardiac Arrest 67 25.092
308
P TRM003 Tremor 54 25.092
309
P ATS364 Autism 70 25.032
310
P ANP001 Anaplastic Large Cell Lymphoma 58 25.032
311
PLS009 Plasma Cell Neoplasm 51 25.032
312
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 24.972
313
STM007 Stomatitis 50 24.972
314
P SCH015 Schizophrenia 74 24.913
315
P LTR001 Lateral Sclerosis 54 24.913
316
SCR001 Secretory Meningioma 41 24.672
317
LYM002 Lymphoplasmacyte-Rich Meningioma 36 24.672
318
SQM013 Squamous Cell Carcinoma, Head and Neck 80 24.551
319
THY111 Thyroid Carcinoma, Familial Medullary 67 24.551
320
P SYP003 Syphilis 58 24.551
321
ALL006 Allergic Asthma 56 24.551
322
P GLM040 Glioma Susceptibility 1 81 24.490
323
BRR014 Barrett Esophagus 65 24.490
324
P END044 Endometriosis 63 24.490
325
HYP005 Hypokalemia 55 24.429
326
TRM010 Traumatic Brain Injury 51 24.429
327
P GRF003 Graft-Versus-Host Disease 72 24.306
328
P EPL164 Epilepsy 71 24.306
329
PRT036 Peritonitis 64 24.306
330
VRL011 Viral Infectious Disease 61 24.183
331
PRD004 Prediabetes Syndrome 47 24.183
332
P MSC003 Muscular Atrophy 52 24.121
333
THY125 Thyroid Gland Medullary Carcinoma 50 24.121
334
P ATR011 Atrial Fibrillation 66 24.060
335
P CHR345 Chronic Pain 44 24.060
336
MCL079 Macular Telangiectasia Type 2 27 24.060
337
SQM002 Squamous Cell Papilloma 46 23.997
338
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 23.935
339
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 23.935
340
P CHR071 Charcot-Marie-Tooth Disease 65 23.810
341
P AST007 Astrocytoma 51 23.810
342
NRR001 Neuroretinitis 42 23.747
343
GST045 Gastroenteritis 59 23.685
344
INT007 Intermediate Coronary Syndrome 55 23.621
345
HMP009 Haemophilus Influenzae 43 23.621
346
c ACT073 Acute Leukemia 58 23.558
347
P HDC001 Headache 57 23.558
348
RTN023 Retinitis 46 23.558
349
CHL079 Children's Interstitial Lung Disease 26 23.558
350
GT001 Gout 64 23.495
351
P PLY014 Polycystic Kidney Disease 62 23.495
352
PLM033 Pulmonary Embolism 59 23.495
353
CRB004 Cerebral Artery Occlusion 45 23.495
354
c LKM005 Leukemia, T-Cell, Chronic 34 23.495
355
ART016 Aortic Aneurysm 69 23.431
356
SPN186 Spinal Cord Injury 60 23.431
357
ACT088 Acute Insulin Response 41 23.431
358
INS024 Insulin-Like Growth Factor I 79 23.367
359
LSH001 Leishmaniasis 63 23.367
360
SFT003 Soft Tissue Sarcoma 56 23.367
361
P ART021 Arteriosclerosis 54 23.367
362
HYP014 Hyperuricemia 52 23.367
363
BCK006 Back Pain 42 23.367
364
P KLZ004 Kala-Azar 1 41 23.367
365
MTY003 Mutyh Polyposis 30 23.367
366
c PLM164 Pulmonary Hypertension, Primary, 1 75 23.304
367
P RTN024 Retinoblastoma 73 23.304
368
P HYD006 Hydrocephalus 66 23.304
369
MSL001 Measles 62 23.304
370
PNC041 Pancreatic Ductal Adenocarcinoma 51 23.304
371
CHL014 Cholera 59 23.175
372
ACS001 Acoustic Neuroma 56 23.175
373
PRP030 Purpura 54 23.175
374
HYP081 Hypolipoproteinemia 51 23.175
375
P MLT020 Multiple Sclerosis 72 23.111
376
P HYP076 Hyperthyroidism 55 23.111
377
DYS073 Dysphagia 50 23.046
378
c FML008 Familial Retinoblastoma 53 22.981
379
P BPL003 Bipolar Disorder 56 22.851
380
c DNG003 Dengue Disease 59 22.786
381
PRS045 Prostatic Hypertrophy 53 22.786
382
MYC088 Mycobacterium Avium Complex Infections 29 22.720
383
P NPH012 Nephrotic Syndrome 60 22.588
384
MCS002 Mucositis 56 22.588
385
DNT012 Dental Caries 53 22.588
386
AND005 Androgen Insensitivity Syndrome, Mild 19 22.588
387
CRB037 Cerebral Palsy 69 22.522
388
P FLL037 Follicular Lymphoma 67 22.522
389
P NSP012 Nasopharyngeal Carcinoma 66 22.522
390
P END033 Endocarditis 57 22.522
391
P ALC033 Alcohol Use Disorder 58 22.389
392
c MJR024 Major Affective Disorder 9 41 22.389
393
c MJR022 Major Affective Disorder 8 38 22.389
394
P HNT016 Huntington Disease 72 22.323
395
P SLP005 Sleep Disorder 59 22.256
396
OTT002 Otitis Media 72 22.189
397
ATR057 Atrioventricular Block 55 22.189
398
P TBR001 Tuberous Sclerosis 70 22.121
399
P HML002 Hemolytic Anemia 63 22.054
400
P RCT021 Rectum Cancer 52 22.054
401
c MLG068 Malignant Glioma 46 22.054
402
P RHB003 Rhabdomyosarcoma 63 21.986
403
INS001 Insulinoma 60 21.918
404
P HML001 Hemolytic-Uremic Syndrome 53 21.918
405
P MYC084 Mycobacterium Tuberculosis 1 68 21.850
406
P INS002 in Situ Carcinoma 53 21.850
407
P LCT001 Lactic Acidosis 51 21.850
408
P FBR017 Fibrosarcoma 56 21.781
409
P CNR004 Cone-Rod Dystrophy 2 73 21.713
410
CHL068 Cholestasis 61 21.713
411
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 21.713
412
PRS021 Prostatic Adenoma 51 21.713
413
c LKM063 Leukemia, Chronic Myeloid 72 21.644
414
P CND004 Candidiasis 58 21.644
415
SPL018 Splenomegaly 48 21.644
416
ACT113 Acute Myeloblastic Leukemia with Maturation 46 21.644
417
FCT007 Factor Vii Deficiency 67 21.575
418
HMS001 Hemosiderosis 54 21.575
419
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 21.506
420
PRS129 Prostatic Hyperplasia, Benign 49 21.506
421
BRK010 Burkitt Lymphoma 67 21.436
422
ALL014 Allergic Encephalomyelitis 38 21.436
423
MLR004 Malaria 81 21.366
424
c HMC039 Hemochromatosis, Type 1 74 21.366
425
TTH006 Tooth Disease 46 21.366
426
P CNJ013 Conjunctivitis 65 21.296
427
c CHR064 Chronic Monocytic Leukemia 33 21.296
428
c PSR017 Psoriasis 2 53 21.226
429
P MCR010 Microcephaly 59 21.156
430
ATN005 Autonomic Dysfunction 46 21.156
431
LWC002 Lowe Oculocerebrorenal Syndrome 65 21.085
433
CHL065 Cholangiocarcinoma 68 21.014
434
OCL006 Ocular Hypertension 53 21.014
435
LMY002 Leiomyoma 52 21.014
436
c PCH010 Pachyonychia Congenita 3 44 21.014
437
P RRH023 Rare Hereditary Hemochromatosis 41 21.014
438
c OVR114 Ovarian Cancer 1 38 21.014
439
P LNG028 Long Qt Syndrome 66 20.943
440
KRT019 Keratitis, Hereditary 65 20.943
441
P HYP265 Hypotonia 43 20.943
442
c CHR682 Chronic Bilirubin Encephalopathy 39 20.943
443
c DLT002 Dilated Cardiomyopathy 79 20.872
444
RNL065 Renal Cell Carcinoma, Papillary, 1 73 20.872
445
P GCH001 Gaucher's Disease 63 20.872
446
RTN017 Retinal Detachment 61 20.872
447
P BND020 Bone Disease 59 20.872
448
P UVT001 Uveitis 57 20.872
449
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 20.800
450
BRN024 Bronchitis 68 20.728
451
c VRL010 Viral Hepatitis 52 20.728
452
INT079 Intrahepatic Cholangiocarcinoma 51 20.584
453
MYL005 Myelofibrosis 70 20.511
454
c SCL052 Scleroderma, Familial Progressive 61 20.511
455
P DBT005 Diabetes Insipidus 55 20.511
456
WST005 West Nile Virus 54 20.511
457
PNC129 Pancreatic Adenocarcinoma 68 20.439
458
P THY032 Thyroiditis 52 20.439
459
c PSR023 Psoriasis 1 52 20.439
460
P BNG032 Benign Mesothelioma 46 20.439
461
CRD132 Cardiac Conduction Defect 58 20.365
462
CRN030 Coronary Stenosis 50 20.365
463
RTC005 Reticulosarcoma 47 20.365
464
P SYS005 Systemic Scleroderma 68 20.292
465
P CLC063 Celiac Disease 1 66 20.292
466
c PSR028 Psoriasis 7 42 20.292
467
c PSR032 Psoriasis 11 47 20.218
468
c PSR018 Psoriasis 13 41 20.218
469
c ATS007 Autism Spectrum Disorder 67 20.144
470
P SKN015 Skin Carcinoma 66 20.144
471
P GST044 Gastritis 56 20.144
472
TRN015 Transient Cerebral Ischemia 63 20.070
473
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 20.070
474
DSS008 Disease of Mental Health 58 20.070
475
c FML035 Familial Hyperlipidemia 55 20.070
476
P MYP006 Myopia 55 19.921
477
c ACR116 Aicardi-Goutieres Syndrome 1 52 19.921
478
ORL015 Oral Squamous Cell Carcinoma 43 19.921
479
OVR094 Ovarian Epithelial Cancer 38 19.921
480
P ACR001 Aicardi-Goutieres Syndrome 62 19.846
481
P MYC008 Myocarditis 59 19.846
482
SNS003 Sensory Peripheral Neuropathy 54 19.771
483
P DYS154 Dystonia 65 19.695
484
P PRS038 Personality Disorder 65 19.695
485
LYM027 Lymphopenia 58 19.695
486
P ANT006 Antiphospholipid Syndrome 55 19.695
487
c GLC092 Glaucoma, Primary Open Angle 62 19.619
488
SPN051 Spondylitis 51 19.619
489
JNT004 Joint Laxity, Short Stature, and Myopia 45 19.619
490
P HMN010 Hemangioma 61 19.543
491
DRM011 Dermatophytosis 52 19.543
492
KRT009 Keratosis 51 19.543
493
P MLG074 Malignant Mesenchymoma 40 19.543
494
BRN028 Brain Cancer 74 19.467
495
MNT001 Mantle Cell Lymphoma 69 19.467
496
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 19.390
497
INF009 Inflammatory Spondylopathy 31 19.390
498
c LKM060 Leukemia, Acute Lymphoblastic 3 56 19.313
499
NRF007 Neurofibroma 64 19.235
500
OST017 Osteomyelitis 64 19.235
501
P SNS001 Sensorineural Hearing Loss 60 19.235
502
BRN002 Bronchiolitis 59 19.235
503
P SPP010 Suppressor of Tumorigenicity 3 51 19.235
504
P LMY004 Leiomyosarcoma 63 19.157
505
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 19.157
506
P THY023 Thymoma 65 19.079
507
c THY107 Thymoma, Familial 52 19.079
508
c BLD140 Blood Group, I System 32 19.079
509
P SHR029 Short Syndrome 63 19.001
510
P ESP024 Esophagitis 62 19.001
511
TRN018 Transitional Cell Carcinoma 56 19.001
512
HMC014 Homocysteinemia 53 19.001
513
SXL003 Sexual Disorder 47 19.001
514
HDN002 Head Injury 46 19.001
515
DNG002 Dengue Hemorrhagic Fever 60 18.922
516
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 18.922
517
CNT047 Contact Dermatitis 58 18.922
518
P CHL066 Cholangitis 51 18.843
519
P OVR082 Overgrowth Syndrome 50 18.843
520
HRT011 Heart Septal Defect 50 18.843
521
MDD011 Mood Disorder 62 18.764
522
PRP016 Paraplegia 52 18.764
523
PTH003 Pathologic Nystagmus 52 18.764
524
FBR054 Fibroma 44 18.764
525
P RTN008 Retinitis Pigmentosa 79 18.684
526
SYN036 Syncope 45 18.684
527
c DRM054 Dermatitis, Atopic, 2 44 18.684
528
c GCH015 Gaucher Disease, Type I 70 18.604
529
P URT039 Urticaria 58 18.604
530
P RTN018 Retinal Disease 53 18.604
531
PPL052 Papillomatosis, Confluent and Reticulated 33 18.604
532
P TXP001 Toxoplasmosis 60 18.524
533
P SPN046 Spinal Muscular Atrophy 62 18.443
534
c MLG084 Malignant Fibrous Histiocytoma 63 18.362
535
DBT006 Diabetic Macular Edema 48 18.362
536
P ATT013 Attention Deficit-Hyperactivity Disorder 65 18.281
537
P PLY018 Polycythemia 56 18.281
538
P SCK005 Sickle Cell Disease 50 18.281
539
NSS002 Neisseria Meningitidis Infection 47 18.281
540
CLF001 Cleft Lip 53 18.199
541
GTR002 Goiter 53 18.199
542
P DDN001 Duodenal Ulcer 52 18.199
543
c BTT014 Beta-Thalassemia 74 18.117
544
BRT054 Brittle Bone Disorder 72 18.117
545
OST003 Osteonecrosis 61 18.117
546
ETN001 Eating Disorder 60 18.117
547
GNG013 Gingivitis 59 18.117
548
GST023 Gastric Ulcer 53 18.117
549
MSC157 Muscular Dystrophy, Duchenne Type 72 18.034
550
P HYP061 Hypertrophic Cardiomyopathy 70 18.034
551
P CYS018 Cystitis 59 18.034
552
PLM134 Pulmonary Fibrosis, Idiopathic 77 17.951
553
CLF027 Cleft Palate, Isolated 64 17.951
554
P ART023 Arthropathy 62 17.951
555
IGR001 Ige Responsiveness, Atopic 59 17.951
556
END040 Endogenous Depression 55 17.951
557
INH023 Inherited Cancer-Predisposing Syndrome 46 17.951
558
NPH009 Nephrolithiasis 55 17.868
559
P ECL001 Eclampsia 50 17.868
560
HST010 Histiocytosis 48 17.868
561
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 17.784
562
c EPS035 Episodic Ataxia, Type 2 63 17.700
563
RNL077 Renal Fibrosis 47 17.700
564
MTB004 Metabolic Acidosis 50 17.616
565
OST062 Osteoarthritis with Mild Chondrodysplasia 47 17.616
566
RST023 Resting Heart Rate, Variation in 41 17.616
567
KPS004 Kaposi Sarcoma 75 17.531
568
GST092 Gastroesophageal Reflux 67 17.531
569
MSC007 Muscle Hypertrophy 64 17.531
570
ORL011 Oral Cancer 60 17.531
571
SCH014 Schistosomiasis 57 17.531
572
P SBS003 Substance Abuse 55 17.531
573
DWR001 Dwarfism 44 17.531
574
P PYL005 Pyelonephritis 56 17.446
575
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 17.446
576
P ART005 Arteriovenous Malformation 65 17.360
577
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 17.360
578
PSR001 Psoriatic Arthritis 61 17.360
579
KRT006 Keratoconjunctivitis 53 17.360
580
BCK003 Background Diabetic Retinopathy 46 17.360
581
NRL016 Neural Tube Defects 82 17.274
582
CNN005 Connective Tissue Disease 68 17.274
583
c INF071 Inflammatory Bowel Disease 1 67 17.274
584
BRC012 Brucellosis 64 17.274
585
AYM001 Ayme-Gripp Syndrome 57 17.274
586
PLM010 Pulmonary Edema 54 17.274
587
NRT001 Neurotic Disorder 53 17.274
588
P HMP007 Hemophilia 51 17.274
589
ENT011 Enterocolitis 51 17.274
590
CLR108 Colorectal Adenoma 64 17.187
591
c LPM012 Lipomatosis, Multiple 60 17.187
592
RBS001 Rabies 58 17.187
593
NRN004 Neuroendocrine Tumor 55 17.187
594
P TRT010 Teratoma 52 17.187
595
c TBR025 Tuberous Sclerosis 1 77 17.100
596
P MLN007 Male Infertility 55 17.100
597
PRC013 Pericarditis 54 17.013
598
P PTS002 Ptosis 53 17.013
599
c HNT004 Huntington Disease-Like 2 50 17.013
600
DBT004 Diabetic Polyneuropathy 49 17.013
601
DBT002 Diabetic Autonomic Neuropathy 41 17.013
602
GST040 Gastric Adenocarcinoma 70 16.925
603
PSY004 Psychotic Disorder 67 16.925
604
HLC007 Helicobacter Pylori Infection 59 16.925
605
P GRV001 Graves' Disease 55 16.925
606
CLR030 Clear Cell Renal Cell Carcinoma 53 16.925
607
c DRR009 Diarrhea 6 46 16.925
608
P MDL005 Medulloblastoma 77 16.836
609
P NRV007 Nervous System Disease 66 16.836
610
c WLM018 Wilms Tumor 5 61 16.836
611
HRP004 Herpes Zoster 60 16.836
612
PRT013 Portal Hypertension 59 16.836
613
GST050 Gastrointestinal System Disease 56 16.836
614
SYN007 Synovitis 54 16.836
615
PLC002 Plica Syndrome 36 16.836
616
c PLM128 Pulmonary Hypertension, Primary, 2 29 16.836
617
P RTT002 Rett Syndrome 80 16.748
618
PFF001 Pfeiffer Syndrome 79 16.748
619
P EPS003 Episodic Ataxia 59 16.748
620
PST092 Posttransplant Acute Limbic Encephalitis 29 16.748
621
PLY001 Polycythemia Vera 69 16.658
622
KHL003 Kohlschutter-Tonz Syndrome 65 16.658
623
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 16.658
624
LMB062 Limb Ischemia 55 16.658
625
P STR020 Strabismus 55 16.658
626
PLM005 Pleomorphic Lipoma 40 16.658
627
P ASP006 Aspergillosis 69 16.568
628
P CRN037 Craniosynostosis 68 16.568
629
CTN007 Cutaneous Leishmaniasis 62 16.568
630
P PRM006 Primary Biliary Cirrhosis 62 16.568
631
PPT005 Peptic Ulcer Disease 59 16.568
632
c MYT020 Myotonic Dystrophy 2 57 16.568
633
P RTN016 Retinal Degeneration 53 16.568
634
FDL002 Food Allergy 51 16.568
635
MCH006 Mechanical Strabismus 42 16.568
636
c BSL007 Basal Cell Carcinoma 68 16.478
637
P RBL001 Rubella 59 16.478
638
NSP002 Nasopharyngitis 43 16.478
639
MDD018 Middle East Respiratory Syndrome 43 16.478
640
P ALP009 Alopecia Areata 60 16.387
641
49X006 49, Xxxxy Syndrome 41 16.387
642
P MYS003 Myasthenia Gravis 68 16.296
643
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 16.204
644
TYP007 Typhoid Fever 63 16.204
645
INT002 Intermittent Claudication 61 16.204
646
PRT058 Pure Autonomic Failure 59 16.204
647
PNC001 Pancytopenia 54 16.204
648
CRH005 Crohn's Colitis 53 16.204
650
P VNT002 Ventricular Septal Defect 60 16.112
651
P MYS005 Myositis 56 16.112
652
ECH003 Echinococcosis 53 16.112
653
SPS057 Spasticity 45 16.112
654
IRR002 Irritable Bowel Syndrome 65 16.019
655
P MCH002 Machado-Joseph Disease 62 16.019
656
c ACT135 Acute Graft Versus Host Disease 52 16.019
657
MXD026 Mixed Glioma 45 16.019
658
PLY150 Polykaryocytosis Inducer 31 16.019
659
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 15.926
660
YLL002 Yellow Fever 61 15.926
661
ERY051 Erythroleukemia, Familial 56 15.926
662
THY030 Thyroid Gland Disease 52 15.926
663
RTN020 Retinal Vascular Disease 46 15.926
664
GST019 Gastrointestinal Stromal Tumor 78 15.832
665
P FML011 Familial Adenomatous Polyposis 72 15.832
666
MYL031 Myeloproliferative Neoplasm 66 15.832
667
c PRM005 Primary Hyperparathyroidism 58 15.832
668
PLS011 Plasmacytoma 56 15.832
669
MST005 Mastitis 53 15.832
670
P ESS003 Essential Thrombocythemia 68 15.737
671
P BNG030 Benign Ependymoma 60 15.737
672
ILS001 Ileus 51 15.737
673
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 15.642
674
EWN003 Ewing Sarcoma 69 15.642
675
P VNW001 Von Willebrand's Disease 65 15.642
676
c ATM011 Autoimmune Hepatitis 63 15.642
677
HMT002 Hematologic Cancer 62 15.642
678
CHL067 Cholecystitis 57 15.642
679
PNM008 Pneumothorax 56 15.642
680
P ADL017 Adult T-Cell Leukemia 56 15.642
681
P CHN012 Chondrosarcoma 56 15.642
682
c LKM056 Leukemia, Chronic Lymphocytic 2 48 15.642
683
c HYP272 Hypercholesterolemia, Familial, 3 44 15.642
684
IDP070 Idiopathic Scoliosis 42 15.642
685
APN008 Apnea, Obstructive Sleep 64 15.546
686
P SJG008 Sjogren Syndrome 61 15.546
687
DSS009 Disseminated Intravascular Coagulation 57 15.546
688
RLP002 Relapsing-Remitting Multiple Sclerosis 56 15.546
689
CLL010 Cellular Ependymoma 54 15.546
690
CRT013 Carotid Stenosis 50 15.546
691
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 15.546
692
VRC005 Varicose Veins 60 15.450
693
P MMP001 Mumps 58 15.450
694
c ACT134 Acute Liver Failure 56 15.450
695
INF034 Infective Endocarditis 53 15.450
696
PNT038 Peanut Allergy 45 15.450
697
MTH009 Mouth Disease 56 15.353
698
HRY003 Hairy Cell Leukemia 55 15.353
699
LYM040 Lymphoblastic Lymphoma 54 15.353
700
MNN020 Meningococcal Infection 46 15.353
701
SCK003 Sickle Cell Anemia 74 15.256
702
c PRG042 Progressive Familial Heart Block, Type Ia 69 15.256
703
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 15.256
704
P MVM001 Movement Disease 63 15.256
705
VSC002 Vascular Dementia 57 15.256
706
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 15.256
707
P CTN015 Cutaneous T Cell Lymphoma 49 15.256
708
ANX004 Anoxia 40 15.256
709
CRP001 Carpal Tunnel Syndrome 67 15.158
710
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 15.158
711
P MTR014 Motor Neuron Disease 65 15.158
712
APP008 Appendicitis 61 15.158
713
c LNG047 Long Qt Syndrome 2 58 15.158
714
P MMB011 Membranous Nephropathy 50 15.158
715
ACR007 Acromegaly 71 15.059
716
P BRN022 Bronchiectasis 59 15.059
717
CLF004 Cleft Lip/palate 54 15.059
718
AMN001 Amenorrhea 54 15.059
719
CLL003 Cellulitis 54 15.059
720
P LCH002 Lichen Planus 53 15.059
721
NRT004 Neuritis 52 15.059
722
CLN015 Colon Adenocarcinoma 65 14.959
723
P PRP029 Porphyria 62 14.959
724
BLR008 Bilirubin Metabolic Disorder 57 14.959
725
CYT008 Cytomegalovirus Infection 57 14.959
726
P PMP001 Pemphigus 54 14.959
727
c MTR002 Mitral Valve Insufficiency 48 14.959
728
c INC015 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2 37 14.959
729
c RNG015 Ring Chromosome 2 26 14.959
730
c LPD015 Lipodystrophy, Familial Partial, Type 2 64 14.859
731
P LYM033 Lymphoproliferative Syndrome 59 14.859
732
HMG005 Hemoglobinopathy 56 14.859
733
c THY109 Thyroid Cancer, Nonmedullary, 1 56 14.859
734
P HYP730 Hypogonadotropic Hypogonadism 52 14.859
735
CHR074 Choriocarcinoma 47 14.859
736
MYT011 Myotonia 34 14.859
737
P LPS002 Liposarcoma 65 14.759
738
TBC004 Tobacco Addiction 64 14.759
739
c ALP101 Alpha-Thalassemia 62 14.759
740
c WLF013 Wolfram Syndrome 1 60 14.759
741
HYD002 Hydronephrosis 60 14.759
742
P OPT006 Optic Nerve Disease 60 14.759
743
APR001 Apraxia 52 14.759
744
RDN001 Reading Disorder 40 14.759
745
c JVN010 Juvenile Rheumatoid Arthritis 64 14.657
746
P DRM010 Dermatomyositis 61 14.657
747
STT001 Status Epilepticus 60 14.657
748
LNG108 Langerhans Cell Histiocytosis 58 14.657
749
P PRG013 Paraganglioma 52 14.657
750
AST006 Astigmatism 47 14.657
751
KHN001 Kuhnt-Junius Degeneration 47 14.657
752
P VSC018 Visceral Steatosis 33 14.657
753
c NRF024 Neurofibromatosis, Type I 77 14.555
754
P APL001 Aplastic Anemia 74 14.555
755
ING001 Inguinal Hernia 60 14.555
756
GLS018 Glass Syndrome 57 14.555
757
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 14.555
758
PLR008 Pleurisy 50 14.555
759
VLV047 Volvulus of Midgut 49 14.555
760
IGG001 Iga Glomerulonephritis 48 14.555
761
BRN056 Bronchopulmonary Dysplasia 57 14.452
762
APH002 Aphasia 57 14.452
763
BRN004 Brain Edema 56 14.452
764
THR004 Thrombocytosis 51 14.452
765
MCR004 Macroglobulinemia 49 14.452
766
c FLL041 Follicular Lymphoma 1 49 14.452
767
FCL012 Facial Paralysis 46 14.452
768
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 14.452
769
P INC033 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 2 30 14.452
770
c TBR026 Tuberous Sclerosis 2 72 14.349
771
INT066 Interstitial Lung Disease 60 14.349
772
P NRC002 Narcolepsy 52 14.349
773
SBC016 Subacute Delirium 44 14.349
774
KRN002 Kearns-Sayre Syndrome 63 14.244
775
c DWL002 Dowling-Degos Disease 1 58 14.244
776
c MST023 Mesothelioma, Malignant 57 14.244
777
MCL027 Macular Dystrophy, Dominant Cystoid 50 14.244
778
MNN009 Meningoencephalitis 49 14.244
779
LWC001 Low Compliance Bladder 43 14.244
780
CHG001 Chagas Disease 66 14.139
781
P HYP024 Hypoparathyroidism 56 14.139
782
BCT002 Bacterial Vaginosis 53 14.139
783
P RNL017 Renal Oncocytoma 53 14.139
784
ART074 Aortic Dissection 52 14.139
785
CRD137 Cardiogenic Shock 47 14.139
786
TNP001 Tinea Pedis 46 14.139
787
MCL003 Macular Holes 40 14.139
788
c FML001 Familial Atrial Fibrillation 65 14.033
789
ACT119 Acute Promyelocytic Leukemia 63 14.033
790
P GLY013 Glycogen Storage Disease 60 14.033
791
P BRS044 Breast Adenocarcinoma 59 14.033
792
ALL010 Allergic Contact Dermatitis 56 14.033
793
HPT022 Hepatoblastoma 56 14.033
794
P PNC025 Panic Disorder 53 14.033
795
c HMP029 Hemophilia a 67 13.927
796
P ADL010 Adult Respiratory Distress Syndrome 65 13.927
797
NPH091 Nephrolithiasis, Calcium Oxalate 60 13.927
798
VSC003 Visceral Leishmaniasis 55 13.927
799
FNG017 Fungal Infectious Disease 53 13.927
800
ENT004 Enthesopathy 49 13.927
801
P RRT020 Rare Tumor 41 13.927
802
c EXD008 Exudative Vitreoretinopathy 1 71 13.819
803
MYC006 Mycosis Fungoides 66 13.819
804
BLL006 Bullous Pemphigoid 62 13.819
805
AVN001 Avian Influenza 59 13.819
806
MCR013 Microphthalmia 57 13.819
807
P FCL005 Focal Segmental Glomerulosclerosis 57 13.819
808
EXP004 Exophthalmos 52 13.819
809
URL001 Urolithiasis 45 13.819
811
PTT037 Pituitary Tumors 44 13.819
812
P MLG056 Malignant Hyperthermia 67 13.711
813
LPR001 Lepromatous Leprosy 50 13.711
814
P SCL009 Sclerosing Cholangitis 48 13.711
815
P MYC033 Myoclonus 46 13.711
816
NWC001 Newcastle Disease 45 13.711
817
GLC008 Glucose Metabolism Disease 40 13.711
818
c SYS043 Systemic Lupus Erythematosus 1 38 13.711
819
BLD163 Blood Group, Dombrock System 24 13.711
820
c FML021 Familial Hypercholesterolemia 66 13.601
821
ANT024 Anthrax Disease 58 13.601
822
P INT068 Intestinal Disease 53 13.601
823
CHR073 Choreatic Disease 52 13.601
824
P SML001 Small Cell Carcinoma 52 13.601
825
PLS007 Plasmodium Falciparum Malaria 52 13.601
826
c SCN007 Secondary Hyperparathyroidism 51 13.601
827
URM002 Uremia 49 13.601
828
DRY001 Dry Eye Syndrome 47 13.601
829
P TTR001 Tetralogy of Fallot 70 13.491
830
LYM021 Lymphadenitis 57 13.491
831
NRM004 Neuroma 51 13.491
832
VTM002 Vitamin B12 Deficiency 48 13.491
833
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 13.491
834
SMN007 Seminoma 43 13.491
835
NRN002 Neuronitis 32 13.491
836
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 13.491
837
KWS002 Kawasaki Disease 65 13.380
838
ANG020 Angiosarcoma 64 13.380
839
P ANG015 Angioedema 57 13.380
840
P RST001 Restless Legs Syndrome 54 13.380
841
INT075 Intracranial Hypertension 53 13.380
842
GRN017 Granulocytopenia 44 13.380
843
P SCL057 Scoliosis, Isolated 1 41 13.380
844
c CHR020 Chronic Interstitial Cystitis 37 13.380
845
c MYC058 Myocardial Infarction 2 34 13.380
846
XRD010 Xeroderma Pigmentosum, Variant Type 73 13.268
847
P AGM001 Agammaglobulinemia 65 13.268
848
P INT070 Intestinal Obstruction 58 13.268
849
c BCT007 Bacterial Meningitis 55 13.268
850
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 13.268
851
P ICH004 Ichthyosis 54 13.268
852
P EPD016 Epidermolysis Bullosa 53 13.268
853
P HYP040 Hypospadias 51 13.268
854
P CRN025 Corneal Dystrophy 49 13.268
855
ALB002 Albinism 46 13.268
856
P PRM002 Primary Hyperoxaluria 62 13.155
857
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 13.155
858
P PTN014 Patent Ductus Arteriosus 1 60 13.155
859
PHR003 Pharyngitis 57 13.155
860
c CNT035 Central Nervous System Disease 52 13.155
861
DMY004 Demyelinating Disease 52 13.155
862
MRG003 Marginal Zone B-Cell Lymphoma 52 13.155
863
PHN003 Phenylketonuria 75 13.041
864
c WLM013 Wilms Tumor 1 65 13.041
865
CRD223 Cardiac Arrhythmia 60 13.041
866
P WRD001 Waardenburg's Syndrome 59 13.041
867
THY122 Thyroid Gland Cancer 57 13.041
868
PRP036 Peripheral T-Cell Lymphoma 53 13.041
869
c GRS014 Griscelli Syndrome, Type 2 50 13.041
870
URT010 Ureteral Obstruction 45 13.041
871
NRM005 Neuromuscular Disease 64 12.926
872
CRC021 Carcinosarcoma 62 12.926
873
P CHR285 Chronic Myelomonocytic Leukemia 60 12.926
874
P EHL001 Ehlers-Danlos Syndrome 58 12.926
875
P SLM003 Salmonellosis 55 12.926
876
TND005 Tendinitis 54 12.926
877
P MTR003 Mitral Valve Stenosis 50 12.926
878
KRT001 Keratoconjunctivitis Sicca 49 12.926
879
KRT002 Keratomalacia 47 12.926
880
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 12.926
881
TRG019 Trigonocephaly with Short Stature and Developmental Delay 32 12.926
882
CHR619 Chromosome 2q35 Duplication Syndrome 62 12.811
883
SRC027 Sarcoma, Synovial 58 12.811
884
c ATM024 Autoimmune Pancreatitis 55 12.811
885
NRL002 Neurilemmomatosis 51 12.811
886
CLR109 Colorectal Adenocarcinoma 51 12.811
887
HYP748 Hypertelorism 50 12.811
888
NRN001 Neuroendocrine Carcinoma 47 12.811
889
CRB009 Cerebritis 37 12.811
890
CRT084 Creatinine Clearance Quantitative Trait Locus 25 12.811
891
CHR072 Chordoma 58 12.694
892
ERY003 Erythema Multiforme 58 12.694
893
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 12.694
894
AMB002 Amblyopia 49 12.694
895
HYP043 Hyperandrogenism 48 12.694
896
PSD009 Pseudohermaphroditism 46 12.694
897
GRW007 Growth Hormone Deficiency 46 12.694
898
RFR003 Refractive Error 43 12.694
899
SPP007 Suppression Amblyopia 39 12.694
900
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 12.575
901
ART002 Arts Syndrome 64 12.575
902
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 12.575
903
P CNT004 Centronuclear Myopathy 59 12.575
904
FBR047 Fibromyalgia 58 12.575
905
P PTT006 Pituitary Adenoma 55 12.575
906
HRT012 Heart Valve Disease 53 12.575
907
P GRS003 Griscelli Syndrome 53 12.575
908
c HYP602 Hyperoxaluria, Primary, Type Ii 51 12.575
909
SPN019 Spondylolisthesis 51 12.575
910
HYP781 Hypoascorbemia 51 12.575
911
RDC002 Radiculopathy 50 12.575
912
P TMP001 Temporal Lobe Epilepsy 50 12.575
913
c HYP555 Hypertriglyceridemia, Transient Infantile 39 12.575
914
HML018 Homologous Wasting Disease 22 12.575
915
P OLG002 Oligodendroglioma 67 12.456
916
LYM017 Lyme Disease 64 12.456
917
IRN001 Iron Deficiency Anemia 59 12.456
918
APP015 Apparent Mineralocorticoid Excess 58 12.456
919
HMP005 Hemiplegia 55 12.456
920
P ACT008 Actinic Keratosis 53 12.456
921
LRN003 Learning Disability 49 12.456
922
c HMN021 Human T-Cell Leukemia Virus Type 1 47 12.456
923
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 12.456
924
c HMN022 Human T-Cell Leukemia Virus Type 2 37 12.456
925
TMR016 Tumor Suppressor Gene on Chromosome 11 28 12.456
926
FLL027 Fallopian Tube Carcinoma 67 12.336
927
PPL049 Papillon-Lefevre Syndrome 65 12.336
928
HSH003 Hashimoto Thyroiditis 62 12.336
929
P INT143 Interstitial Cystitis 61 12.336
930
c JVN061 Juvenile Arthritis 60 12.336
931
P GLL018 Gallbladder Cancer 57 12.336
932
CHK001 Chikungunya 57 12.336
933
JPN002 Japanese Encephalitis 57 12.336
934
GNR004 Generalized Anxiety Disorder 56 12.336
935
PRS047 Prostatitis 56 12.336
936
P SHR001 Short Bowel Syndrome 53 12.336
937
P HMR003 Hemorrhagic Disease 53 12.336
938
c HRD202 Hereditary Lymphedema I 50 12.336
939
HMP001 Hemopericardium 48 12.336
940
AND014 Androgenic Alopecia 46 12.336
941
P SBR004 Seborrheic Dermatitis 45 12.336
942
OCL015 Oculomotor Apraxia 37 12.336
943
END072 Endotheliitis 35 12.336
944
BLD165 Blood Group, Colton System 20 12.336
945
VNH007 Von Hippel-Lindau Syndrome 73 12.214
946
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 12.214
947
PRN019 Perinatal Necrotizing Enterocolitis 59 12.214
948
c CHL119 Cholangitis, Primary Sclerosing 57 12.214
949
VGN023 Vaginitis 54 12.214
950
P FML023 Familial Hemiplegic Migraine 53 12.214
951
DYS015 Dysentery 52 12.214
952
P ALP061 Alopecia, Androgenetic, 1 49 12.214
953
MNG006 Monogenic Diabetes 46 12.214
954
FBR019 Fibromatosis 41 12.214
955
PRS063 Paresthesia 41 12.214
956
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 12.214
957
CRY035 Cryptorchidism, Unilateral or Bilateral 58 12.092
958
CHR177 Chromophobe Renal Cell Carcinoma 57 12.092
959
LMY014 Leiomyoma, Uterine 56 12.092
960
EMB004 Embryonal Carcinoma 56 12.092
961
ORL005 Oral Candidiasis 56 12.092
962
P HMP002 Hemophagocytic Lymphohistiocytosis 54 12.092
963
P KRT007 Keratoconus 50 12.092
964
CHL004 Cholelithiasis 49 12.092
965
P GND004 Gonadal Dysgenesis 48 12.092
966
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 12.092
967
RYN005 Raynaud Phenomenon 47 12.092
968
P WSK001 Wiskott-Aldrich Syndrome 72 11.968
969
ADN011 Adenoid Cystic Carcinoma 70 11.968
970
P FRN006 Frontotemporal Dementia 68 11.968
971
CMM005 Common Cold 57 11.968
972
NPH003 Nephrocalcinosis 51 11.968
973
FSC004 Fasciitis 50 11.968
974
PLP001 Pulpitis 49 11.968
975
c BCT013 Bacterial Pneumonia 48 11.968
976
DGN001 Degenerative Disc Disease 48 11.968
977
P GNG009 Gangliosidosis 44 11.968
978
HPT070 Hepatosplenic T-Cell Lymphoma 38 11.968
979
P AXN001 Axonal Neuropathy 36 11.968
980
P LYN001 Lynch Syndrome 77 11.842
981
P MST009 Mastocytosis 64 11.842
982
DCB001 Decubitus Ulcer 61 11.842
983
DCT002 Ductal Carcinoma in Situ 59 11.842
984
c GRV008 Graves Disease 1 56 11.842
985
GST037 Gastroparesis 54 11.842
986
MMM001 Mammary Paget's Disease 53 11.842
987
c GLL024 Gallbladder Disease 1 53 11.842
988
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 11.842
989
THR016 Thrombophlebitis 51 11.842
990
LFT001 Left Bundle Branch Hemiblock 49 11.842
991
PLL012 Pollen Allergy 46 11.842
992
DNG001 Dengue Shock Syndrome 43 11.842
993
END041 Endometrial Adenocarcinoma 63 11.716
994
THR100 Thrombocytopenic Purpura, Autoimmune 60 11.716
995
P ATR010 Atrial Heart Septal Defect 60 11.716
996
P LKD001 Leukodystrophy 59 11.716
997
P MLN069 Melanoma, Uveal 59 11.716
998
PST028 Post-Traumatic Stress Disorder 58 11.716
999
TRD006 Tardive Dyskinesia 54 11.716
1000
LYM022 Lymphangioma 54 11.716
1001
ASP003 Aseptic Meningitis 51 11.716
1002
AZS001 Azoospermia 50 11.716
1003
TRY001 Trypanosomiasis 50 11.716
1004
QDR001 Quadriplegia 48 11.716
1005
CHR176 Chromophil Renal Cell Carcinoma 23 11.716
1006
c FNC027 Fanconi Anemia, Complementation Group a 81 11.588
1007
c CNG006 Congenital Hypothyroidism 64 11.588
1008
PLG002 Plague 63 11.588
1009
NWB001 Newborn Respiratory Distress Syndrome 58 11.588
1010
P PRN023 Prion Disease 57 11.588
1011
P LRY044 Larynx Cancer 55 11.588
1012
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 11.588
1013
P END047 Endophthalmitis 53 11.588
1014
ALL009 Allergic Conjunctivitis 50 11.588
1015
BCT004 Bacteriuria 49 11.588
1016
HYP068 Hyperostosis 48 11.588
1017
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 48 11.588
1018
ACT055 Actinomycosis 47 11.588
1019
ATM052 Autoimmune Disease 1 37 11.588
1020
HND015 Hand Skill, Relative 33 11.588
1021
c ART101 Aortic Valve Disease 2 65 11.458
1022
c CHR417 Chronic Graft Versus Host Disease 57 11.458
1023
P PLY041 Polymyositis 57 11.458
1024
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 11.458
1025
TCK001 Tick-Borne Encephalitis 56 11.458
1026
FLR002 Filariasis 55 11.458
1027
AMN003 Amnestic Disorder 54 11.458
1028
P FBR031 Febrile Seizures 53 11.458
1029
c WRD033 Waardenburg Syndrome, Type 2e 53 11.458
1030
P THR015 Thrombophilia 51 11.458
1031
PLC008 Placenta Disease 50 11.458
1032
NTR046 Neutrophil Migration 50 11.458
1033
P OBS001 Obstructive Jaundice 50 11.458
1034
CYN002 Cyanosis, Transient Neonatal 45 11.458
1035
PPL001 Papillary Adenoma 44 11.458
1036
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 11.458
1037
HRP008 Herpes Simiae 25 11.458
1039
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 11.327
1040
BLD131 Bladder Urothelial Carcinoma 62 11.327
1041
P GLL022 Guillain-Barre Syndrome 59 11.327
1042
P PLY006 Polydactyly 59 11.327
1043
INC002 Inclusion Body Myositis 58 11.327
1044
CRY005 Cryptococcosis 58 11.327
1045
MMB001 Membranoproliferative Glomerulonephritis 55 11.327
1046
HDR002 Hidradenitis Suppurativa 55 11.327
1047
FCL014 Focal Epilepsy 54 11.327
1048
INT051 Intussusception 53 11.327
1049
P PRC012 Pericardial Effusion 51 11.327
1050
P RNL015 Renal Hypertension 47 11.327
1051
CNT033 Central Nervous System Cancer 47 11.327
1052
DYS018 Dysostosis 44 11.327
1053
BCL014 B-Cell Growth Factor 35 11.327
1054
GRM010 Germ Cells Tumors 34 11.327
1055
c PLM121 Pulmonary Hypertension, Primary, 4 28 11.327
1056
HDG004 Hodgkin's Granuloma 23 11.327
1057
HDG006 Hodgkin's Paragranuloma 22 11.327
1058
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 11.195
1059
c HPT007