Search results for Tetrahydrofolyl-[Glu](n)

3667 hits were found for Tetrahydrofolyl-[Glu](n)

# Family MCID Name MIFTS Score
1
P NRB001 Neuroblastoma 72 95.569
2
P ADN016 Adenocarcinoma 64 79.052
3
HLX001 Helix Syndrome 47 75.598
4
P ENC004 Encephalitis 61 69.388
5
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 61.829
6
P BLD134 Bladder Cancer 79 60.012
7
c DNT047 Dentinogenesis Imperfecta Type 2 31 57.612
8
RPD005 Rapidly Involuting Congenital Hemangioma 38 56.475
9
P CLR023 Colorectal Cancer 99 50.331
10
P KDN018 Kidney Disease 72 50.331
11
P BRS047 Breast Cancer 97 48.792
12
ADN018 Adenoma 59 48.083
13
48X005 48,xyyy 39 47.363
14
P HPT023 Hepatocellular Carcinoma 100 45.724
15
PRT037 Pertussis 65 45.641
16
ISC004 Ischemia 58 45.473
17
HRW001 Hair Whorl 36 45.473
18
HMN044 Human Immunodeficiency Virus Type 1 71 43.850
19
MYX011 Myxozoa 17 42.435
20
P GST053 Gastric Cancer 83 42.165
21
P LYM118 Lymphoma 68 40.029
22
c PLM127 Pulmonary Hypertension, Primary, 3 34 39.260
23
P ALZ034 Alzheimer Disease 88 38.771
24
P SZR006 Seizure Disorder 56 38.771
25
P PNC035 Pancreatic Cancer 84 38.474
26
P LVR013 Liver Disease 68 38.474
27
P OVR042 Ovarian Cancer 88 38.275
28
P HNT016 Huntington Disease 72 38.076
29
P TRT010 Teratoma 52 37.774
30
VSL002 Visual Epilepsy 59 37.673
31
P LKM002 Leukemia 68 37.163
32
PPL022 Papilloma 54 36.854
33
47X002 47,xyy 49 36.750
34
P GLM045 Glioma 63 36.542
35
ATM095 Autoimmune Disease 62 36.437
36
P HRP006 Herpes Simplex 65 36.016
37
CNG034 Congestive Heart Failure 69 35.910
38
P NRP001 Neuropathy 56 35.803
39
c AMY091 Amyotrophic Lateral Sclerosis 1 89 35.590
40
P LTR001 Lateral Sclerosis 54 35.590
41
c SVR001 Severe Acute Respiratory Syndrome 62 35.375
42
GLL048 Glial Tumor 45 35.050
43
ESP021 Esophageal Cancer 90 34.941
44
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 34.722
45
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 34.501
46
SQM002 Squamous Cell Papilloma 46 34.168
47
c CHR684 Chronic Kidney Disease 70 33.944
48
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 33.944
49
BNR002 Bone Resorption Disease 48 33.944
50
P LNG032 Lung Cancer 98 33.718
51
HYP066 Hyperglycemia 61 33.491
52
P PRS040 Prostate Cancer 97 33.377
53
P RTN016 Retinal Degeneration 53 33.262
54
ALL026 Allergic Hypersensitivity Disease 62 33.148
55
c ACT071 Acute Kidney Failure 60 32.800
56
VCC001 Vaccinia 49 32.800
57
GLB015 Glioblastoma Multiforme 75 32.684
58
P MLN008 Melanoma 69 32.567
59
P MYL006 Myeloid Leukemia 60 32.214
60
STM007 Stomatitis 50 31.495
61
c PCH010 Pachyonychia Congenita 3 44 31.495
62
LSH001 Leishmaniasis 63 31.129
63
P ENC018 Encephalopathy 61 31.129
64
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 31.129
65
P KLZ004 Kala-Azar 1 41 31.129
66
PLM129 Pulmonary Disease, Chronic Obstructive 73 30.883
67
P PHC003 Pheochromocytoma 71 30.883
68
P PLM036 Pulmonary Fibrosis 65 30.635
69
P CHR345 Chronic Pain 44 30.635
70
ADR040 Adrenal Gland Pheochromocytoma 46 30.511
71
LPP008 Lipoprotein Quantitative Trait Locus 62 30.385
72
LVR012 Liver Cirrhosis 62 30.259
73
c MCR113 Microvascular Complications of Diabetes 3 52 30.259
74
PNG002 Pain Agnosia 51 30.259
75
c MCR120 Microvascular Complications of Diabetes 7 47 30.259
76
c MCR130 Microvascular Complications of Diabetes 6 41 30.259
77
c MCR133 Microvascular Complications of Diabetes 4 41 30.259
78
CYS001 Cystic Fibrosis 81 30.133
79
P HRT032 Heart Disease 75 30.133
80
DPR016 Depression 63 30.133
81
P BPL003 Bipolar Disorder 56 30.133
82
P WSK001 Wiskott-Aldrich Syndrome 72 30.006
83
P FBR017 Fibrosarcoma 56 30.006
84
P SCH015 Schizophrenia 74 29.879
85
c LKM061 Leukemia, Acute Myeloid 84 29.751
86
MNT002 Mental Depression 58 29.751
87
P DRR001 Diarrhea 55 29.751
88
c MJR024 Major Affective Disorder 9 41 29.622
89
c MJR022 Major Affective Disorder 8 38 29.622
90
P MYP004 Myopathy 70 29.364
91
HMP009 Haemophilus Influenzae 43 29.233
92
OVR109 Ovarian Germ Cell Teratoma 32 29.233
93
TRT017 Teratoma, Ovarian 29 29.233
94
LNG099 Lung Disease 60 28.707
95
P RTN024 Retinoblastoma 73 28.573
96
BRN024 Bronchitis 68 28.440
97
c FML008 Familial Retinoblastoma 53 28.440
98
DRM006 Dermatitis 61 28.170
99
VRC005 Varicose Veins 60 28.170
100
P HYP724 Hyperlipoproteinemia, Type Iii 73 28.034
101
P PRP019 Peripheral Nervous System Disease 58 28.034
102
OST159 Osteogenic Sarcoma 66 27.898
103
BRN071 Brain Injury 49 27.898
104
ALC007 Alcohol Dependence 66 27.761
105
CNT047 Contact Dermatitis 58 27.761
106
c ACT075 Acute Myocardial Infarction 57 27.761
107
END086 End Stage Renal Disease 51 27.761
108
P INS002 in Situ Carcinoma 53 27.623
109
TXC005 Toxic Shock Syndrome 62 27.484
110
PRC051 Paracetamol Poisoning 30 27.484
111
ACT133 Acetylation, Slow 23 27.345
112
c ATM075 Autoimmune Encephalitis 38 27.205
113
TRM010 Traumatic Brain Injury 51 27.065
114
NCT003 N-Acetylglutamate Synthase Deficiency 45 26.924
115
P BCL017 B-Cell Lymphoma 58 26.781
116
ART140 Arteries, Anomalies of 52 26.781
117
IMM167 Immune Deficiency Disease 78 26.639
118
P TRM003 Tremor 54 26.639
119
RTN023 Retinitis 46 26.639
120
NRR001 Neuroretinitis 42 26.639
121
P RTN008 Retinitis Pigmentosa 79 26.495
122
P LNG064 Lung Cancer Susceptibility 3 78 26.495
123
ATH013 Atherosclerosis Susceptibility 65 26.495
124
CYT002 Cytokine Deficiency 42 26.495
125
P NSP012 Nasopharyngeal Carcinoma 66 26.205
126
P BRS044 Breast Adenocarcinoma 59 26.205
127
P PRK057 Parkinson Disease, Late-Onset 78 26.059
128
P VSC007 Vascular Disease 63 26.059
129
CHL014 Cholera 59 26.059
130
c ACT134 Acute Liver Failure 56 26.059
131
P PLY019 Polyneuropathy 56 26.059
132
CRB004 Cerebral Artery Occlusion 45 26.059
133
SVR004 Severe Combined Immunodeficiency 73 25.765
134
P CTR002 Cataract 60 25.616
135
CRT002 Cartilage-Hair Hypoplasia 59 25.616
136
GST040 Gastric Adenocarcinoma 70 25.467
137
HYP266 Hypoxia 57 25.467
138
c HPT073 Hepatitis C Virus 72 25.317
139
P MJR001 Major Depressive Disorder 68 25.317
140
P MSC005 Muscular Dystrophy 66 25.317
141
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 25.317
142
TRN018 Transitional Cell Carcinoma 56 25.317
143
FTT001 Fatty Liver Disease 61 25.166
144
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 25.014
145
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 25.014
146
TTN003 Tetanus 65 25.014
147
THY029 Thyroid Carcinoma 59 24.861
148
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 24.861
149
P MYC007 Myocardial Infarction 70 24.707
150
c HYP595 Hypertension, Essential 84 24.552
151
P MCR115 Microvascular Complications of Diabetes 5 66 24.552
152
MYL069 Myeloma, Multiple 85 24.396
153
RNL114 Renal Cell Carcinoma, Nonpapillary 78 24.396
154
OST012 Osteoarthritis 78 24.396
155
PRT036 Peritonitis 64 24.396
156
P GST044 Gastritis 56 24.396
157
BCT022 Bacterial Infectious Disease 56 24.239
158
SQM006 Squamous Cell Carcinoma 60 24.081
159
PPL052 Papillomatosis, Confluent and Reticulated 33 24.081
160
P CRN300 Coronary Heart Disease 1 63 23.762
161
c SYS001 Systemic Lupus Erythematosus 86 23.601
162
HYP056 Hypoglycemia 66 23.439
163
P INF037 Inflammatory Bowel Disease 54 23.439
164
P PLM037 Pulmonary Hypertension 67 23.276
165
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 23.276
166
CLN015 Colon Adenocarcinoma 65 23.276
167
CNV004 Canavan Disease 61 23.276
168
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 23.276
169
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 23.276
170
P DBT009 Diabetes Mellitus 64 23.111
171
ALL010 Allergic Contact Dermatitis 56 23.111
172
ATS010 Autosomal Recessive Disease 48 23.111
173
CHG001 Chagas Disease 66 22.945
174
c SML038 Small Cell Cancer of the Lung 65 22.945
175
c PRC016 Pre-Eclampsia 63 22.945
176
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 30 22.945
177
P ART005 Arteriovenous Malformation 65 22.778
178
GST045 Gastroenteritis 59 22.778
179
P ALC033 Alcohol Use Disorder 58 22.778
180
LYS002 Lysosomal Storage Disease 52 22.610
181
MDD018 Middle East Respiratory Syndrome 43 22.610
182
ANX010 Anxiety 73 22.441
183
SPN186 Spinal Cord Injury 60 22.441
184
STT001 Status Epilepticus 60 22.441
185
P ATS364 Autism 70 22.270
186
P AMY004 Amyloidosis 70 22.270
187
RBS001 Rabies 58 22.270
188
P KDN017 Kidney Cancer 60 22.098
189
P MYT002 Myotonic Dystrophy 49 22.098
190
P LKM062 Leukemia, Acute Lymphoblastic 69 21.925
191
CHL123 Chlamydia 59 21.925
192
INS024 Insulin-Like Growth Factor I 79 21.750
193
c ATR087 Atrial Standstill 1 75 21.750
194
ULC004 Ulcerative Colitis 73 21.750
195
c MGR028 Migraine with or Without Aura 1 67 21.750
196
PST092 Posttransplant Acute Limbic Encephalitis 29 21.750
197
ARG004 Argyria 27 21.750
198
PLM134 Pulmonary Fibrosis, Idiopathic 77 21.397
199
CRB039 Cerebrovascular Disease 67 21.397
200
P PLY011 Polycystic Ovary Syndrome 56 21.397
201
P MVM001 Movement Disease 63 21.218
202
MSL001 Measles 62 21.218
203
OCL069 Ocular Motor Apraxia 51 21.218
204
P RHB003 Rhabdomyosarcoma 63 21.037
205
P PRN023 Prion Disease 57 21.037
206
P INF038 Influenza 68 20.855
207
NNL005 Non-Alcoholic Fatty Liver Disease 61 20.855
208
P INF032 Infertility 57 20.855
209
MST005 Mastitis 53 20.855
210
P ANX007 Anauxetic Dysplasia 1 46 20.855
211
MST004 Mast Cell Neoplasm 42 20.855
212
EXT007 Extracutaneous Mastocytoma 38 20.855
213
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 20.855
214
P FRG001 Fragile X Syndrome 70 20.671
215
c ACT027 Acute Pancreatitis 60 20.671
216
THY006 Thymus Lymphoma 26 20.671
217
c HYP836 Hypercholesterolemia, Familial, 1 73 20.486
218
P NTR004 Neutropenia 63 20.486
219
c SCL052 Scleroderma, Familial Progressive 61 20.486
220
P GLM007 Glomerulonephritis 57 20.486
221
P CRD246 Cardiovascular System Disease 57 20.486
222
P HPT021 Hepatitis 67 20.299
223
P ANP001 Anaplastic Large Cell Lymphoma 58 20.299
224
ERY051 Erythroleukemia, Familial 56 20.299
226
c PLM164 Pulmonary Hypertension, Primary, 1 75 20.110
227
P RSP003 Respiratory Failure 74 20.110
228
OBS002 Obsessive-Compulsive Disorder 68 20.110
229
PLY150 Polykaryocytosis Inducer 31 20.110
230
PSY004 Psychotic Disorder 67 19.919
231
LPD008 Lipid Metabolism Disorder 62 19.919
232
CLT003 Colitis 62 19.919
233
P EXN002 Exanthem 57 19.919
234
SLC006 Silicosis 56 19.919
235
SLP001 Sleeping Sickness 54 19.919
236
ORL011 Oral Cancer 60 19.727
237
PLM033 Pulmonary Embolism 59 19.727
238
TRY001 Trypanosomiasis 50 19.532
239
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 19.532
240
AST005 Asthma 76 19.336
241
P EPL164 Epilepsy 71 19.336
242
DWN001 Down Syndrome 70 19.336
243
P GCH001 Gaucher's Disease 63 19.336
244
ACQ007 Acquired Immunodeficiency Syndrome 60 19.336
245
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 19.336
246
PLM010 Pulmonary Edema 54 19.336
247
HMC014 Homocysteinemia 53 19.336
248
c MLN055 Melanoma, Cutaneous Malignant 10 52 19.336
249
c PLM128 Pulmonary Hypertension, Primary, 2 29 19.336
250
MTH071 Methane Production 26 19.336
251
c LKM063 Leukemia, Chronic Myeloid 72 19.138
252
c MCP052 Mucopolysaccharidosis, Type Vi 67 19.138
253
c RHB024 Rhabdomyosarcoma 2 67 19.138
254
MDD011 Mood Disorder 62 19.138
255
c HPT016 Hepatitis B 59 19.138
256
P BNG032 Benign Mesothelioma 46 19.138
257
ALL014 Allergic Encephalomyelitis 38 19.138
258
c LKM005 Leukemia, T-Cell, Chronic 34 19.138
259
c DLT002 Dilated Cardiomyopathy 79 18.937
260
P OST002 Osteoporosis 74 18.937
261
P MLT020 Multiple Sclerosis 72 18.735
262
MYL009 Myelodysplastic Syndrome 70 18.735
263
ANG054 Angina Pectoris 66 18.735
264
P MDL005 Medulloblastoma 77 18.530
265
c ACT068 Acute Cystitis 63 18.530
266
P LPS004 Lupus Erythematosus 61 18.530
267
PRS045 Prostatic Hypertrophy 53 18.530
268
ORL015 Oral Squamous Cell Carcinoma 43 18.530
269
ANP008 Anaplastic Oligoastrocytoma 30 18.530
270
P ATX030 Ataxia-Telangiectasia 82 18.323
271
P HYP061 Hypertrophic Cardiomyopathy 70 18.323
272
P THR014 Thrombocytopenia 67 18.323
273
P END044 Endometriosis 63 18.323
274
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 18.323
275
PRT013 Portal Hypertension 59 18.323
276
P RHN004 Rhinitis 57 18.323
277
P HDC001 Headache 57 18.323
278
P TRN020 Turner Syndrome 67 18.114
279
P ATR011 Atrial Fibrillation 66 18.114
280
P ATT013 Attention Deficit-Hyperactivity Disorder 65 18.114
281
INT007 Intermediate Coronary Syndrome 55 18.114
282
NNL006 Non-Alcoholic Steatohepatitis 54 18.114
283
P MSC003 Muscular Atrophy 52 18.114
284
P MCL001 Mucolipidosis 48 18.114
285
SCR011 Scrapie 39 18.114
286
EWN003 Ewing Sarcoma 69 17.902
287
c ATS007 Autism Spectrum Disorder 67 17.902
288
VSC003 Visceral Leishmaniasis 55 17.902
289
TLN003 Telangiectasis 52 17.902
290
TRT001 Teratocarcinoma 45 17.902
291
P SCH017 Schindler Disease 33 17.902
292
CRV035 Cervical Cancer 76 17.687
293
ART016 Aortic Aneurysm 69 17.687
294
c HPT001 Hepatitis C 62 17.687
295
DPH001 Diphtheria 60 17.687
296
P BND020 Bone Disease 59 17.687
297
SCH014 Schistosomiasis 57 17.687
298
AMN003 Amnestic Disorder 54 17.687
299
P AST007 Astrocytoma 51 17.687
300
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 17.687
301
END057 Endometrial Cancer 74 17.470
302
XRD010 Xeroderma Pigmentosum, Variant Type 73 17.470
303
DFC004 Deficiency Anemia 70 17.470
304
SKN019 Skin Melanoma 68 17.470
305
c MCR129 Microvascular Complications of Diabetes 1 66 17.470
306
P PRD008 Periodontitis 64 17.470
307
RTN017 Retinal Detachment 61 17.470
308
P CYS018 Cystitis 59 17.470
309
EMB004 Embryonal Carcinoma 56 17.470
310
AGN016 Aging 56 17.470
311
HYP060 Hyperinsulinism 54 17.470
312
P GNG009 Gangliosidosis 44 17.470
313
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 17.251
314
ALL003 Allergic Rhinitis 67 17.251
315
SKN016 Skin Disease 63 17.251
316
c WLM018 Wilms Tumor 5 61 17.251
317
c ACT073 Acute Leukemia 58 17.251
318
P RCT021 Rectum Cancer 52 17.251
319
PRS021 Prostatic Adenoma 51 17.251
320
CCN002 Cocaine Abuse 49 17.251
321
NWC001 Newcastle Disease 45 17.251
322
ATX019 Ataxia with Vitamin E Deficiency 42 17.251
323
P TYS001 Tay-Sachs Disease 69 17.028
324
CHL065 Cholangiocarcinoma 68 17.028
325
PNC129 Pancreatic Adenocarcinoma 68 17.028
326
P CRD119 Cardiac Arrest 67 17.028
327
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 17.028
328
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 17.028
329
P SKN015 Skin Carcinoma 66 17.028
330
P MNN013 Meningitis 66 17.028
331
c MCP001 Mucopolysaccharidosis Iii 65 17.028
332
P PNC044 Pancreatitis 61 17.028
333
ANT024 Anthrax Disease 58 17.028
334
KRT009 Keratosis 51 17.028
335
INT079 Intrahepatic Cholangiocarcinoma 51 17.028
336
P TMP001 Temporal Lobe Epilepsy 50 17.028
337
PRS129 Prostatic Hyperplasia, Benign 49 17.028
338
c MCR112 Microvascular Complications of Diabetes 2 41 17.028
339
ANX004 Anoxia 40 17.028
340
c GCH015 Gaucher Disease, Type I 70 16.802
341
P DNG005 Dengue Virus 59 16.802
342
HMS001 Hemosiderosis 54 16.802
343
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 16.802
344
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 16.802
345
ADG002 Audiogenic Seizures 25 16.802
346
P RHM011 Rheumatoid Arthritis 80 16.574
347
PLM001 Pulmonary Tuberculosis 69 16.574
348
c MCL062 Mucolipidosis Ii Alpha/beta 68 16.574
349
P DYS154 Dystonia 65 16.574
350
ANR040 Aneurysm 59 16.574
351
P PSR002 Psoriasis 62 16.342
352
CHL068 Cholestasis 61 16.342
353
P CND004 Candidiasis 58 16.342
354
PST011 Pustulosis of Palm and Sole 52 16.342
355
P OVR082 Overgrowth Syndrome 50 16.342
356
c CNG411 Congenital Disorder of Glycosylation, Type in 68 16.107
357
P ADL010 Adult Respiratory Distress Syndrome 65 16.107
358
P THL005 Thalassemia 60 16.107
359
P MCR010 Microcephaly 59 16.107
360
IRN002 Iron Metabolism Disease 57 16.107
361
P SBS003 Substance Abuse 55 16.107
362
P RTN018 Retinal Disease 53 16.107
363
PNC041 Pancreatic Ductal Adenocarcinoma 51 16.107
364
HND015 Hand Skill, Relative 33 16.107
365
MLR004 Malaria 81 15.868
366
STR067 Stroke, Ischemic 81 15.868
367
P SYS005 Systemic Scleroderma 68 15.868
368
P DMN002 Dementia 66 15.868
369
NTR005 Nutritional Deficiency Disease 62 15.868
370
GLC003 Glucose Intolerance 54 15.868
371
SPN035 Spindle Cell Sarcoma 53 15.868
372
CLR109 Colorectal Adenocarcinoma 51 15.868
373
NNK001 Nonaka Myopathy 46 15.868
374
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 15.868
375
KPS004 Kaposi Sarcoma 75 15.626
376
P FML011 Familial Adenomatous Polyposis 72 15.626
377
INS001 Insulinoma 60 15.626
378
P LKD001 Leukodystrophy 59 15.626
379
AVN001 Avian Influenza 59 15.626
380
PPT005 Peptic Ulcer Disease 59 15.626
381
GST023 Gastric Ulcer 53 15.626
382
ATN005 Autonomic Dysfunction 46 15.626
383
P RRH023 Rare Hereditary Hemochromatosis 41 15.626
384
OBN001 Ouabain Resistance 18 15.626
385
BRN028 Brain Cancer 74 15.380
386
LYM133 Lymphoma, Hodgkin, Classic 69 15.380
387
P HYP086 Hypothyroidism 69 15.380
388
P PNM007 Pneumonia 68 15.380
389
CLF027 Cleft Palate, Isolated 64 15.380
390
P PLY014 Polycystic Kidney Disease 62 15.380
391
c BRN108 Branchiootic Syndrome 1 62 15.380
392
P HMN010 Hemangioma 61 15.380
393
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 15.380
394
EYD002 Eye Disease 58 15.380
395
END040 Endogenous Depression 55 15.380
396
P SCK005 Sickle Cell Disease 50 15.380
397
RNL077 Renal Fibrosis 47 15.380
398
CRT084 Creatinine Clearance Quantitative Trait Locus 25 15.380
399
P LKM071 Leukemia, Chronic Lymphocytic 79 15.130
400
P FRN006 Frontotemporal Dementia 68 15.130
401
SRC014 Sarcoma 65 15.130
402
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 15.130
403
HLC007 Helicobacter Pylori Infection 59 15.130
404
P ANG015 Angioedema 57 15.130
405
P MLN007 Male Infertility 55 15.130
406
P ATR005 Atrophic Gastritis 50 15.130
407
GLY015 Glycine N-Methyltransferase Deficiency 39 15.130
408
ADL002 Adult Syndrome 70 14.875
409
BRK010 Burkitt Lymphoma 67 14.875
410
c DBT099 Diabetes Mellitus, Type I 65 14.875
411
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 14.875
412
PLG002 Plague 63 14.875
413
HYD002 Hydronephrosis 60 14.875
414
BRN004 Brain Edema 56 14.875
415
TRC010 Trichotillomania 51 14.875
416
NTR046 Neutrophil Migration 50 14.875
417
MTB004 Metabolic Acidosis 50 14.875
418
CCN001 Cocaine Dependence 48 14.875
419
PTT037 Pituitary Tumors 44 14.875
420
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 14.875
421
PRP027 Peripheral Vascular Disease 71 14.617
422
P HYD006 Hydrocephalus 66 14.617
423
P THY023 Thymoma 65 14.617
424
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 14.617
425
NRM005 Neuromuscular Disease 64 14.617
426
CRD223 Cardiac Arrhythmia 60 14.617
427
c MCP044 Mucopolysaccharidosis, Type Iiib 59 14.617
428
P PYL005 Pyelonephritis 56 14.617
429
P HYP076 Hyperthyroidism 55 14.617
430
P ALP008 Alopecia 54 14.617
431
c THY107 Thymoma, Familial 52 14.617
432
c INF145 Infantile Liver Failure Syndrome 1 50 14.617
433
HDN002 Head Injury 46 14.617
434
LMB024 Limbic Encephalitis 41 14.617
435
CHR178 Chromosomal Triplication 35 14.617
436
c MJR003 Major Affective Disorder 6 33 14.617
437
c MJR006 Major Affective Disorder 5 33 14.617
438
P MYC084 Mycobacterium Tuberculosis 1 68 14.353
439
c WLM013 Wilms Tumor 1 65 14.353
440
ANG020 Angiosarcoma 64 14.353
441
TBC004 Tobacco Addiction 64 14.353
442
P HYP069 Hyperparathyroidism 63 14.353
443
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 14.353
444
c DWL002 Dowling-Degos Disease 1 58 14.353
445
c LKM060 Leukemia, Acute Lymphoblastic 3 56 14.353
446
RLP002 Relapsing-Remitting Multiple Sclerosis 56 14.353
447
MTH009 Mouth Disease 56 14.353
448
DBT010 Diabetic Neuropathy 54 14.353
449
KRT006 Keratoconjunctivitis 53 14.353
450
P SPP010 Suppressor of Tumorigenicity 3 51 14.353
451
P ECL001 Eclampsia 50 14.353
452
P BRS053 Breast Fibroadenoma 49 14.353
453
LYM019 Lymphosarcoma 46 14.353
454
HRN029 Hearing Loss, Noise-Induced 37 14.353
455
CHL079 Children's Interstitial Lung Disease 26 14.353
456
CRN311 Coronary Ostial Stenosis or Atresia 20 14.353
457
SQM013 Squamous Cell Carcinoma, Head and Neck 80 14.085
458
CRH001 Crohn's Disease 74 14.085
459
P SLP006 Sleep Apnea 69 14.085
460
SND001 Sandhoff Disease 68 14.085
461
RCK004 Rickets 68 14.085
462
P MTR014 Motor Neuron Disease 65 14.085
463
KWS002 Kawasaki Disease 65 14.085
464
END041 Endometrial Adenocarcinoma 63 14.085
465
TRN015 Transient Cerebral Ischemia 63 14.085
466
CTN007 Cutaneous Leishmaniasis 62 14.085
467
c MCP047 Mucopolysaccharidosis, Type Iva 61 14.085
468
P NPH012 Nephrotic Syndrome 60 14.085
469
MCS002 Mucositis 56 14.085
470
HMN014 Human Immunodeficiency Virus Infectious Disease 55 14.085
471
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 14.085
472
c VRL010 Viral Hepatitis 52 14.085
473
MSN004 Mesenchymal Cell Neoplasm 41 14.085
474
P DRM053 Dermatitis, Atopic 66 13.811
475
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 13.811
476
ALC006 Alcoholic Hepatitis 61 13.811
477
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 13.811
478
DSS008 Disease of Mental Health 58 13.811
479
CNS004 Constipation 58 13.811
480
P GLL018 Gallbladder Cancer 57 13.811
481
PTH003 Pathologic Nystagmus 52 13.811
482
ENT011 Enterocolitis 51 13.811
483
LNG031 Lung Benign Neoplasm 51 13.811
484
P HYP040 Hypospadias 51 13.811
485
URM002 Uremia 49 13.811
486
CYN002 Cyanosis, Transient Neonatal 45 13.811
487
HPT004 Hepatic Coma 45 13.811
488
URL001 Urolithiasis 45 13.811
489
SPS057 Spasticity 45 13.811
490
P HYP265 Hypotonia 43 13.811
491
P MJR007 Major Affective Disorder 1 43 13.811
492
NRL016 Neural Tube Defects 82 13.532
493
P SRC025 Sarcoidosis 1 70 13.532
494
P CNJ013 Conjunctivitis 65 13.532
495
ACT119 Acute Promyelocytic Leukemia 63 13.532
496
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 13.532
497
c HPT003 Hepatitis a 62 13.532
498
NRT001 Neurotic Disorder 53 13.532
499
SPL018 Splenomegaly 48 13.532
500
CRD137 Cardiogenic Shock 47 13.532
501
P VTR007 Vitreoretinopathy 46 13.532
502
CHD004 Chudley-Mccullough Syndrome 46 13.532
503
P SMK004 Smoking As a Quantitative Trait Locus 3 44 13.532
504
c MCL016 Mucolipidosis Iii Gamma 43 13.532
505
MCP033 Mucopolysaccharidoses 38 13.532
506
KNZ001 Kanzaki Disease 37 13.532
507
P GLM040 Glioma Susceptibility 1 81 13.248
508
MSC157 Muscular Dystrophy, Duchenne Type 72 13.248
509
P HML002 Hemolytic Anemia 63 13.248
510
P LMY004 Leiomyosarcoma 63 13.248
511
CRC021 Carcinosarcoma 62 13.248
512
HPT019 Hepatic Encephalopathy 60 13.248
513
P MYC008 Myocarditis 59 13.248
514
DCT002 Ductal Carcinoma in Situ 59 13.248
515
c MCP045 Mucopolysaccharidosis, Type Iiic 59 13.248
516
BRN002 Bronchiolitis 59 13.248
517
c MST023 Mesothelioma, Malignant 57 13.248
518
SYS003 Systolic Heart Failure 49 13.248
519
WTH001 Withdrawal Disorder 48 13.248
520
CHR074 Choriocarcinoma 47 13.248
521
P MYC033 Myoclonus 46 13.248
522
c MLG068 Malignant Glioma 46 13.248
523
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 12.956
524
P LNG028 Long Qt Syndrome 66 12.956
525
P PRS038 Personality Disorder 65 12.956
526
MSC007 Muscle Hypertrophy 64 12.956
527
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 12.956
528
P PRP029 Porphyria 62 12.956
529
c PNS012 Paine Syndrome 61 12.956
530
VRL011 Viral Infectious Disease 61 12.956
531
P PTN014 Patent Ductus Arteriosus 1 60 12.956
532
P URT039 Urticaria 58 12.956
533
THR024 Thrombosis 57 12.956
534
BLR008 Bilirubin Metabolic Disorder 57 12.956
535
VSC002 Vascular Dementia 57 12.956
536
c MCL046 Mucolipidosis Iii Alpha/beta 56 12.956
537
HPT022 Hepatoblastoma 56 12.956
538
DFF005 Diffuse Large B-Cell Lymphoma 55 12.956
539
HRT012 Heart Valve Disease 53 12.956
540
P DDN001 Duodenal Ulcer 52 12.956
541
IMP005 Impotence 52 12.956
542
P OPN001 Open-Angle Glaucoma 49 12.956
543
IGG001 Iga Glomerulonephritis 48 12.956
544
c INH020 Inherited Metabolic Disorder 47 12.956
545
TXC020 Toxic Oil Syndrome 33 12.956
546
FCS014 Fucosidase Regulator 15 12.956
547
P ART022 Arthritis 69 12.658
548
IRR002 Irritable Bowel Syndrome 65 12.658
549
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 12.658
550
P SCL018 Scoliosis 60 12.658
551
SPP011 Suppression of Tumorigenicity 12 59 12.658
552
P PLY018 Polycythemia 56 12.658
553
P NRF002 Neurofibromatosis 56 12.658
554
P LRY044 Larynx Cancer 55 12.658
555
PRP030 Purpura 54 12.658
556
DMY004 Demyelinating Disease 52 12.658
557
URC002 Urea Cycle Disorder 51 12.658
558
P MTH008 Methylmalonic Acidemia 50 12.658
559
THY128 Thyroid Tumor 47 12.658
560
NSS002 Neisseria Meningitidis Infection 47 12.658
561
CVD001 Covid-19 44 12.658
562
c EPS039 Episodic Pain Syndrome, Familial, 1 42 12.658
563
OVR094 Ovarian Epithelial Cancer 38 12.658
564
c PRS136 Prostate Cancer, Hereditary, 6 33 12.658
565
c PRS130 Prostate Cancer, Hereditary, 8 32 12.658
566
CRB041 Carboxypeptidase N Deficiency 24 12.658
567
WLS001 Wilson Disease 71 12.353
568
GT001 Gout 64 12.353
569
PRN019 Perinatal Necrotizing Enterocolitis 59 12.353
570
FBR047 Fibromyalgia 58 12.353
571
APH002 Aphasia 57 12.353
572
JPN002 Japanese Encephalitis 57 12.353
573
P MNC007 Monocytic Leukemia 53 12.353
574
P SML001 Small Cell Carcinoma 52 12.353
575
c MCP046 Mucopolysaccharidosis, Type Iiid 51 12.353
576
SGN002 Signet Ring Cell Adenocarcinoma 45 12.353
577
c GM2006 Gm2 Gangliosidosis 45 12.353
578
c SCH069 Schindler Disease, Type I 37 12.353
579
c MJR008 Major Affective Disorder 2 35 12.353
580
c MJR023 Major Affective Disorder 7 33 12.353
581
c MJR004 Major Affective Disorder 4 28 12.353
582
SCK003 Sickle Cell Anemia 74 12.041
583
c MNN043 Meningioma, Familial 74 12.041
584
P CNR004 Cone-Rod Dystrophy 2 73 12.041
585
LYM143 Lymphoma, Non-Hodgkin, Familial 72 12.041
586
WRN001 Werner Syndrome 69 12.041
587
P HYP098 Hypereosinophilic Syndrome 67 12.041
588
CLR108 Colorectal Adenoma 64 12.041
589
INT323 Intraocular Pressure Quantitative Trait Locus 62 12.041
590
MNN042 Meningioma, Radiation-Induced 62 12.041
591
YLL002 Yellow Fever 61 12.041
592
CHC001 Chickenpox 60 12.041
593
ING001 Inguinal Hernia 60 12.041
594
P BRN022 Bronchiectasis 59 12.041
595
P SLP005 Sleep Disorder 59 12.041
596
PST028 Post-Traumatic Stress Disorder 58 12.041
597
BRN056 Bronchopulmonary Dysplasia 57 12.041
598
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 12.041
599
SPN021 Spinal Meningioma 50 12.041
600
P MTH007 Methemoglobinemia 46 12.041
601
c DRR009 Diarrhea 6 46 12.041
602
SCR001 Secretory Meningioma 41 12.041
603
OGD001 Ogden Syndrome 41 12.041
604
CNN001 Cannabis Dependence 40 12.041
605
LYM002 Lymphoplasmacyte-Rich Meningioma 36 12.041
606
c RNG019 Ring Chromosome 3 22 12.041
607
c THR092 Thrombophilia Due to Thrombin Defect 73 11.719
608
P GRF003 Graft-Versus-Host Disease 72 11.719
609
OTT002 Otitis Media 72 11.719
610
PLM031 Poliomyelitis 64 11.719
611
ANR007 Anorexia Nervosa 63 11.719
612
IDP011 Idiopathic Interstitial Pneumonia 59 11.719
613
MCR013 Microphthalmia 57 11.719
614
c THY109 Thyroid Cancer, Nonmedullary, 1 56 11.719
615
BRN038 Bronchial Disease 53 11.719
616
PRP080 Peripheral Artery Disease 53 11.719
617
HRP009 Herpes Simplex Encephalitis 52 11.719
618
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 11.719
619
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 11.719
620
SLR001 Sialuria 50 11.719
621
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 11.719
622
PPL002 Papillary Carcinoma 47 11.719
623
KRT002 Keratomalacia 47 11.719
624
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 11.719
625
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 11.719
626
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 11.719
627
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 11.719
628
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 11.719
629
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 11.719
630
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 11.719
631
P MRQ003 Morquio Syndrome 37 11.719
632
PRS131 Prostate Cancer/brain Cancer Susceptibility 25 11.719
633
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 11.389
634
P MYS003 Myasthenia Gravis 68 11.389
635
KHL003 Kohlschutter-Tonz Syndrome 65 11.389
636
BRC012 Brucellosis 64 11.389
637
TYP007 Typhoid Fever 63 11.389
638
P SJG008 Sjogren Syndrome 61 11.389
639
P SYP003 Syphilis 58 11.389
640
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 11.389
641
P END033 Endocarditis 57 11.389
642
PLS011 Plasmacytoma 56 11.389
643
SCH003 Schizophreniform Disorder 56 11.389
644
c BCT007 Bacterial Meningitis 55 11.389
645
P ICH004 Ichthyosis 54 11.389
646
CLR030 Clear Cell Renal Cell Carcinoma 53 11.389
647
c GLL024 Gallbladder Disease 1 53 11.389
648
PRP016 Paraplegia 52 11.389
649
CRV040 Cervix Carcinoma 51 11.389
650
P MMB011 Membranous Nephropathy 50 11.389
651
CRN030 Coronary Stenosis 50 11.389
652
ENT004 Enthesopathy 49 11.389
653
ACT084 Acute Stress Disorder 47 11.389
654
CRT015 Carotid Artery Occlusion 45 11.389
655
GRN017 Granulocytopenia 44 11.389
656
MCR011 Microinvasive Gastric Cancer 43 11.389
657
BCK006 Back Pain 42 11.389
658
DDN004 Duodenogastric Reflux 33 11.389
659
PRT112 Portal Hypertension, Noncirrhotic 31 11.389
660
c NRF023 Neurofibromatosis, Type Ii 80 11.049
661
CRT072 Creutzfeldt-Jakob Disease 70 11.049
662
PRP001 Propionic Acidemia 65 11.049
663
c GLC092 Glaucoma, Primary Open Angle 62 11.049
664
P ESP024 Esophagitis 62 11.049
665
NRM019 Neuraminidase Deficiency 62 11.049
666
INT066 Interstitial Lung Disease 60 11.049
667
CRD132 Cardiac Conduction Defect 58 11.049
668
NPH009 Nephrolithiasis 55 11.049
669
P GRV001 Graves' Disease 55 11.049
670
P HMC002 Homocystinuria 53 11.049
671
P MYS079 Miyoshi Muscular Dystrophy 50 11.049
672
HRT011 Heart Septal Defect 50 11.049
673
SBC016 Subacute Delirium 44 11.049
674
CNN002 Cannabis Abuse 44 11.049
675
DWR001 Dwarfism 44 11.049
676
P DYS021 Dysautonomia 39 11.049
677
MYC017 Mycobacterium Kansasii 36 11.049
678
ISL099 Isolated Methylmalonic Acidemia 29 11.049
679
NSY001 N Syndrome 28 11.049
680
BRT054 Brittle Bone Disorder 72 10.698
681
CRB037 Cerebral Palsy 69 10.698
682
P OLG002 Oligodendroglioma 67 10.698
683
THY111 Thyroid Carcinoma, Familial Medullary 67 10.698
684
BRR014 Barrett Esophagus 65 10.698
685
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 10.698
686
P FRD001 Friedreich Ataxia 64 10.698
687
c FNC043 Fanconi Anemia, Complementation Group E 62 10.698
688
P MCH002 Machado-Joseph Disease 62 10.698
689
BLL006 Bullous Pemphigoid 62 10.698
690
BRS099 Breast Ductal Carcinoma 62 10.698
691
P PRM006 Primary Biliary Cirrhosis 62 10.698
692
P SNS001 Sensorineural Hearing Loss 60 10.698
693
P OPT006 Optic Nerve Disease 60 10.698
694
P GLL022 Guillain-Barre Syndrome 59 10.698
695
GST050 Gastrointestinal System Disease 56 10.698
696
HYP005 Hypokalemia 55 10.698
697
NRN004 Neuroendocrine Tumor 55 10.698
698
LMB062 Limb Ischemia 55 10.698
699
SYN007 Synovitis 54 10.698
700
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 10.698
702
ESP002 Esophageal Varix 51 10.698
703
MNN009 Meningoencephalitis 49 10.698
704
ACT029 Acute Interstitial Pneumonia 49 10.698
705
INT067 Interstitial Nephritis 48 10.698
706
c MTR002 Mitral Valve Insufficiency 48 10.698
707
KRT013 Keratolytic Winter Erythema 46 10.698
708
ACT003 Acute Kidney Tubular Necrosis 45 10.698
709
HPT067 Hepatocellular Adenoma 44 10.698
710
SMN007 Seminoma 43 10.698
711
PLC002 Plica Syndrome 36 10.698
712
HNS001 Hansen's Disease 34 10.698
713
c RNG015 Ring Chromosome 2 26 10.698
714
STN013 Stenotrophomonas Maltophilia Infection 25 10.698
715
NCT013 N-Acetylaspartate Deficiency 22 10.698
716
P RTT002 Rett Syndrome 80 10.336
717
c BTT014 Beta-Thalassemia 74 10.336
718
c SPN225 Spondyloarthropathy 1 73 10.336
719
FBR012 Fabry Disease 72 10.336
720
P TBR001 Tuberous Sclerosis 70 10.336
721
P ASP006 Aspergillosis 69 10.336
722
P LPR021 Leprosy 3 69 10.336
723
c BSL007 Basal Cell Carcinoma 68 10.336
724
GST092 Gastroesophageal Reflux 67 10.336
725
KRT019 Keratitis, Hereditary 65 10.336
726
NRF007 Neurofibroma 64 10.336
727
P MST009 Mastocytosis 64 10.336
728
P HYP750 Hypertriglyceridemia, Familial 62 10.336
729
P ART023 Arthropathy 62 10.336
730
P VSC011 Vasculitis 62 10.336
731
BLD131 Bladder Urothelial Carcinoma 62 10.336
732
P THR005 Thrombotic Thrombocytopenic Purpura 61 10.336
733
P VNT002 Ventricular Septal Defect 60 10.336
734
GLB001 Gilbert Syndrome 58 10.336
735
NWB001 Newborn Respiratory Distress Syndrome 58 10.336
736
P CHN012 Chondrosarcoma 56 10.336
737
P ART021 Arteriosclerosis 54 10.336
738
P PTS002 Ptosis 53 10.336
739
TXC002 Toxic Encephalopathy 53 10.336
740
P HMP007 Hemophilia 51 10.336
741
PLS009 Plasma Cell Neoplasm 51 10.336
742
THY125 Thyroid Gland Medullary Carcinoma 50 10.336
743
GLY031 Glycoproteinosis 45 10.336
744
INF159 Infantile Sialic Acid Storage Disease 41 10.336
745
LKP003 Leukoplakia 39 10.336
746
c PLY105 Polycystic Ovary Syndrome 1 38 10.336
747
LCH001 Leech Infestation 35 10.336
748
NRX001 Neuroaxonal Dystrophy 35 10.336
749
CND006 Candida Glabrata 32 10.336
750
c FNC027 Fanconi Anemia, Complementation Group a 81 9.960
751
ADR007 Adrenoleukodystrophy 75 9.960
752
P FLL037 Follicular Lymphoma 67 9.960
754
c ALP101 Alpha-Thalassemia 62 9.960
755
P MTR012 Mitral Valve Disease 58 9.960
756
DSS009 Disseminated Intravascular Coagulation 57 9.960
757
ALL006 Allergic Asthma 56 9.960
758
ATR057 Atrioventricular Block 55 9.960
759
AMB001 Amebiasis 55 9.960
760
P STR020 Strabismus 55 9.960
761
SNS003 Sensory Peripheral Neuropathy 54 9.960
762
DNT012 Dental Caries 53 9.960
763
P OBS001 Obstructive Jaundice 50 9.960
764
KRT001 Keratoconjunctivitis Sicca 49 9.960
765
PTH002 Pathological Gambling 49 9.960
766
c HPT015 Hepatitis D 49 9.960
767
GNG008 Ganglioneuroblastoma 48 9.960
768
c FNC023 Fanconi Anemia, Complementation Group N 48 9.960
769
P MRC003 Mercury Poisoning 48 9.960
770
DRY001 Dry Eye Syndrome 47 9.960
771
MTS001 Mutism 46 9.960
772
PLL012 Pollen Allergy 46 9.960
773
SYN036 Syncope 45 9.960
774
MXD026 Mixed Glioma 45 9.960
775
MCH006 Mechanical Strabismus 42 9.960
776
C1N001 C1 Inhibitor Deficiency 39 9.960
777
GRM010 Germ Cells Tumors 34 9.960
779
c PLM121 Pulmonary Hypertension, Primary, 4 28 9.960
780
ADN011 Adenoid Cystic Carcinoma 70 9.569
781
P TTR001 Tetralogy of Fallot 70 9.569
782
PLY001 Polycythemia Vera 69 9.569
783
CMM004 Common Variable Immunodeficiency 68 9.569
784
AND002 Androgen Insensitivity Syndrome 66 9.569
785
c ART101 Aortic Valve Disease 2 65 9.569
786
APN008 Apnea, Obstructive Sleep 64 9.569
787
c GM1007 Gm1 Gangliosidosis 62 9.569
788
NRM001 Neuromyelitis Optica 61 9.569
789
GST033 Gestational Diabetes 61 9.569
790
P GLY013 Glycogen Storage Disease 60 9.569
791
PRT058 Pure Autonomic Failure 59 9.569
792
CMP010 Complex Regional Pain Syndrome 58 9.569
793
c PRM005 Primary Hyperparathyroidism 58 9.569
794
P EHL001 Ehlers-Danlos Syndrome 58 9.569
795
c MCP004 Mucopolysaccharidosis Iv 57 9.569
796
CMM005 Common Cold 57 9.569
797
P MYS005 Myositis 56 9.569
798
P ADL017 Adult T-Cell Leukemia 56 9.569
799
SFT003 Soft Tissue Sarcoma 56 9.569
800
SML019 Smallpox 56 9.569
801
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 9.569
802
WST005 West Nile Virus 54 9.569
803
c PRD040 Periodontitis, Chronic 53 9.569
804
P LCT001 Lactic Acidosis 51 9.569
805
CCC002 Coccidiosis 51 9.569
806
c VRL007 Viral Encephalitis 51 9.569
807
HYP781 Hypoascorbemia 51 9.569
808
CHR005 Chorioamnionitis 51 9.569
809
HPT014 Hepatorenal Syndrome 50 9.569
810
LNG015 Lingual-Facial-Buccal Dyskinesia 50 9.569
811
HMG002 Hemoglobinuria 50 9.569
812
P RNV001 Renovascular Hypertension 48 9.569
813
DRG003 Drug Dependence 47 9.569
814
P RNL015 Renal Hypertension 47 9.569
815
c HMN021 Human T-Cell Leukemia Virus Type 1 47 9.569
816
GRW007 Growth Hormone Deficiency 46 9.569
817
URT010 Ureteral Obstruction 45 9.569
818
c HYP272 Hypercholesterolemia, Familial, 3 44 9.569
819
c PRM038 Primary Agammaglobulinemia 44 9.569
820
MYC013 Mycobacterium Abscessus 43 9.569
821
c PRG020 Paragangliomas 3 39 9.569
822
PRN029 Parainfluenza Virus Type 3 36 9.569
823
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 9.569
824
MYC015 Mycobacterium Fortuitum 32 9.569
825
MYC019 Mycobacterium Marinum 29 9.569
826
MYP120 Myopathy, Distal, with Rimmed Vacuoles 28 9.569
827
GST019 Gastrointestinal Stromal Tumor 78 9.161
828
CNN005 Connective Tissue Disease 68 9.161
829
c HMP029 Hemophilia a 67 9.161
830
MYL031 Myeloproliferative Neoplasm 66 9.161
831
LYM017 Lyme Disease 64 9.161
832
CYS013 Cystinuria 63 9.161
833
P ANR048 Aniridia 1 63 9.161
834
P SPN046 Spinal Muscular Atrophy 62 9.161
835
c MCP043 Mucopolysaccharidosis, Type Iiia 61 9.161
836
WST001 West Syndrome 61 9.161
837
P TST021 Testicular Germ Cell Tumor 60 9.161
838
ACN002 Acanthosis Nigricans 60 9.161
839
ETN001 Eating Disorder 60 9.161
840
P RBL001 Rubella 59 9.161
841
c LTN004 Late-Onset Retinal Degeneration 59 9.161
842
INC002 Inclusion Body Myositis 58 9.161
843
CRY035 Cryptorchidism, Unilateral or Bilateral 58 9.161
844
P BNC003 Bone Cancer 58 9.161
845
P PRV006 Pervasive Developmental Disorder 57 9.161
846
TRD006 Tardive Dyskinesia 54 9.161
847
LMB002 Lambert-Eaton Myasthenic Syndrome 53 9.161
848
P HML001 Hemolytic-Uremic Syndrome 53 9.161
849
c CNT035 Central Nervous System Disease 52 9.161
850
GNG002 Ganglioneuroma 52 9.161
851
CHR073 Choreatic Disease 52 9.161
852
DYS015 Dysentery 52 9.161
853
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 9.161
854
c SCN036 Secondary Progressive Multiple Sclerosis 51 9.161
855
FDL002 Food Allergy 51 9.161
856
TNG007 Tongue Carcinoma 51 9.161
857
c SCN007 Secondary Hyperparathyroidism 51 9.161
858
URT001 Urethritis 49 9.161
859
VLV047 Volvulus of Midgut 49 9.161
860
P SLL003 Salla Disease 48 9.161
861
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 9.161
862
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 9.161
863
P TRM004 Trimethylaminuria 46 9.161
864
CHL152 Childhood Acute Lymphocytic Leukemia 44 9.161
865
HPT082 Hepatic Adenomas, Familial 44 9.161
866
PRS063 Paresthesia 41 9.161
867
KLB003 Klebsiella Pneumonia 41 9.161
868
ANG049 Angioedema Induced by Ace Inhibitors 40 9.161
869
PLY100 Polyploidy 40 9.161
870
ADP007 Adie Pupil 39 9.161
871
ANG016 Angiokeratoma 38 9.161
872
c OVR114 Ovarian Cancer 1 38 9.161
873
ADR022 Adrenomyeloneuropathy 38 9.161
874
SPS019 Spastic Paraparesis 38 9.161
875
c AGM013 Agammaglobulinemia 1, Autosomal Recessive 36 9.161
876
ATX010 Ataxia Neuropathy Spectrum 34 9.161
877
ACT064 Acute Necrotizing Encephalitis 33 9.161
878
HPT085 Hepatitis, Fulminant Viral 32 9.161
879
HNM002 Hinman Syndrome 27 9.161
880
BLD137 Blood Group--Ahonen 16 9.161
881
LTH004 Lathyrism 16 9.161
882
NCT004 N Acetyltransferase Deficiency 14 9.161
883
c GLY008 Glycogen Storage Disease Ii 70 8.735
884
P SPR120 Supranuclear Palsy, Progressive, 1 68 8.735
885
P CLC063 Celiac Disease 1 66 8.735
886
P GLC113 Galactosemia I 64 8.735
887
P TRC086 Trichohepatoenteric Syndrome 1 62 8.735
888
ASP002 Aspartylglucosaminuria 62 8.735
889
NRL005 Neurilemmoma 60 8.735
890
P ATR010 Atrial Heart Septal Defect 60 8.735
891
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 8.735
892
IGR001 Ige Responsiveness, Atopic 59 8.735
893
GNG013 Gingivitis 59 8.735
894
P NMN002 Niemann-Pick Disease 59 8.735
895
CCC001 Coccidioidomycosis 58 8.735
896
BRS051 Breast Disease 58 8.735
897
LYM027 Lymphopenia 58 8.735
898
P UVT001 Uveitis 57 8.735
899
c VSC019 Vesicoureteral Reflux 1 57 8.735
900
CYT008 Cytomegalovirus Infection 57 8.735
901
PNM008 Pneumothorax 56 8.735
902
NRL004 Neuroleptic Malignant Syndrome 56 8.735
903
BRN012 Bronchiolitis Obliterans 55 8.735
904
P NRM002 Normal Pressure Hydrocephalus 54 8.735
905
THR013 Thoracic Outlet Syndrome 54 8.735
906
P EPD016 Epidermolysis Bullosa 53 8.735
907
INF034 Infective Endocarditis 53 8.735
908
CLF001 Cleft Lip 53 8.735
909
P PNC025 Panic Disorder 53 8.735
910
NRT004 Neuritis 52 8.735
911
LGN006 Legionnaire Disease 52 8.735
912
c CNG191 Congenital Disorder of Glycosylation, Type Iia 51 8.735
913
ILS001 Ileus 51 8.735
914
c ALM001 Al Amyloidosis 50 8.735
915
RTN003 Retinal Ischemia 50 8.735
916
BCT004 Bacteriuria 49 8.735
917
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 8.735
918
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 8.735
919
OST062 Osteoarthritis with Mild Chondrodysplasia 47 8.735
920
TST014 Testicular Cancer 46 8.735
921
CMP034 Complete Androgen Insensitivity Syndrome 46 8.735
922
OBS003 Obsessive-Compulsive Personality Disorder 46 8.735
923
CYS019 Cystathioninuria 45 8.735
924
FBR054 Fibroma 44 8.735
925
P CYS017 Cystic Teratoma 41 8.735
926
EMB007 Embryonal Sarcoma 41 8.735
927
MCL003 Macular Holes 40 8.735
928
TBL003 Tubular Adenocarcinoma 40 8.735
929
AMN007 Aminoacylase 1 Deficiency 36 8.735
930
CYT018 Cytochrome P450 2d6 Variant 27 8.735
931
DMT001 Dimethylglycine Dehydrogenase Deficiency 27 8.735
932
NND011 N,n'-Diphenylthiourea Allergic Contact Dermatitis 5 8.735
933
NND012 N,n'-Diethylthiourea Allergic Contact Dermatitis 5 8.735
934
PHN003 Phenylketonuria 75 8.287
935
ACR007 Acromegaly 71 8.287
936
c MYT021 Myotonic Dystrophy 1 69 8.287
937
PCK003 Pick Disease of Brain 68 8.287
938
c NMN015 Niemann-Pick Disease, Type C1 68 8.287
939
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 8.287
940
P CHR012 Chronic Granulomatous Disease 67 8.287
941
P NRV007 Nervous System Disease 66 8.287
942
P NRN021 Neuronal Ceroid Lipofuscinosis 64 8.287
943
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 8.287
944
c DPH024 Diaphragmatic Hernia, Congenital 63 8.287
945
INT002 Intermittent Claudication 61 8.287
946
SDD001 Sudden Infant Death Syndrome 61 8.287
947
P TXP001 Toxoplasmosis 60 8.287
948
c HRD002 Hereditary Angioedema 60 8.287
949
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 59 8.287
950
P HMN036 Hemangiopericytoma, Malignant 59 8.287
951
CHK001 Chikungunya 57 8.287
952
THY122 Thyroid Gland Cancer 57 8.287
953
PRS047 Prostatitis 56 8.287
954
ORL005 Oral Candidiasis 56 8.287
955
IMM140 Immunodeficiency 47 56 8.287
956
P PNM006 Pneumoconiosis 56 8.287
957
c CNG415 Congenital Disorder of Glycosylation, Type Ia 55 8.287
958
c FML035 Familial Hyperlipidemia 55 8.287
959
P VNS003 Venous Insufficiency 55 8.287
960
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 8.287
961
P TCD001 Tic Disorder 53 8.287
962
RHM028 Rheumatic Heart Disease 53 8.287
963
BCT002 Bacterial Vaginosis 53 8.287
964
GTR002 Goiter 53 8.287
965
TRC003 Trichomoniasis 53 8.287
966
PLS007 Plasmodium Falciparum Malaria 52 8.287
967
P CNG436 Congenital Disorder of Deglycosylation 52 8.287
968
HYP014 Hyperuricemia 52 8.287
969
ONC002 Onchocerciasis 52 8.287
970
c ACT135 Acute Graft Versus Host Disease 52 8.287
971
PRV004 Periventricular Leukomalacia 52 8.287
972
SPN051 Spondylitis 51 8.287
973
P PRC012 Pericardial Effusion 51 8.287
974
P RNL007 Renal Tubular Acidosis 51 8.287
975
SCH012 Schizoaffective Disorder 50 8.287
976
PLR008 Pleurisy 50 8.287
977
AZS001 Azoospermia 50 8.287
978
ECT026 Ectopic Pregnancy 50 8.287
979
c ANM042 Anemia, Congenital Dyserythropoietic, Type Ii 49 8.287
980
P ART018 Aortic Valve Insufficiency 49 8.287
981
P CNG003 Congenital Dyserythropoietic Anemia 49 8.287
982
LRN003 Learning Disability 49 8.287
983
DGN001 Degenerative Disc Disease 48 8.287
984
HMP001 Hemopericardium 48 8.287
985
ANT018 Anthracosis 48 8.287
986
LYM009 Lymphocytic Choriomeningitis 47 8.287
987
RFT001 Rift Valley Fever 47 8.287
988
GST071 Gastrointestinal Carcinoma 47 8.287
989
P OVR046 Ovarian Cyst 47 8.287
990
RTN020 Retinal Vascular Disease 46 8.287
991
MNN020 Meningococcal Infection 46 8.287
992
CRB090 Cerebral Hypoxia 44 8.287
993
TST015 Testicular Disease 43 8.287
994
VRL003 Variola Major 42 8.287
995
EXC002 Exocrine Pancreatic Insufficiency 42 8.287
996
OCL052 Ocular Dominance 42 8.287
997
49X006 49, Xxxxy Syndrome 41 8.287
998
CRN322 Coronavirus Infectious Disease 40 8.287
999
c CHR682 Chronic Bilirubin Encephalopathy 39 8.287
1000
P CRB088 Cerebral Atrophy 37 8.287
1001
INF009 Inflammatory Spondylopathy 31 8.287
1002
HYP346 Hypotrichosis and Recurrent Skin Vesicles 28 8.287
1003
URT049 Urate Oxidase, Pseudogene 25 8.287
1004
HXS001 Hexosaminidase C 11 8.287
1005
c TBR025 Tuberous Sclerosis 1 77 7.813
1006
c EXD008 Exudative Vitreoretinopathy 1 71 7.813
1007
MYL005 Myelofibrosis 70 7.813
1008
c INF071 Inflammatory Bowel Disease 1 67 7.813
1009
P BLD062 Bile Duct Cancer 67 7.813
1010
P VNW001 Von Willebrand's Disease 65 7.813
1011
P CHR071 Charcot-Marie-Tooth Disease 65 7.813
1012
c MLG084 Malignant Fibrous Histiocytoma 63 7.813
1013
MSC152 Muscular Dystrophy, Becker Type 63 7.813
1014
PSR001 Psoriatic Arthritis 61 7.813
1016
OST003 Osteonecrosis 61 7.813
1017
FCS002 Fucosidosis 61 7.813
1018
CHR066 Chronic Fatigue Syndrome 61 7.813
1019
P AXN002 Axenfeld-Rieger Syndrome 59 7.813
1020
P FCL005 Focal Segmental Glomerulosclerosis 57 7.813
1021
P ANT006 Antiphospholipid Syndrome 55 7.813
1022
P MYP006 Myopia 55 7.813
1023
GNG005 Gangliocytoma 55 7.813
1024
ACT058 Active Peptic Ulcer Disease 55 7.813
1025
FLR002 Filariasis 55 7.813
1026
c MYP132 Myopathy, Congenital 55 7.813
1027
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 7.813
1028
DNT005 Dentatorubral-Pallidoluysian Atrophy 54 7.813
1029
OCL006 Ocular Hypertension 53 7.813
1030
GSG001 Gas Gangrene 53 7.813
1031
P LMB006 Limb-Girdle Muscular Dystrophy 53 7.813
1032
c HPT007 Hepatitis E 53 7.813
1033
OVR059 Ovary Adenocarcinoma 53 7.813
1034
ART074 Aortic Dissection 52 7.813
1035
c NMN014 Niemann-Pick Disease, Type C2 51 7.813
1036
P MNN019 Mannosidosis, Beta a, Lysosomal 51 7.813
1037
ACH005 Achalasia 51 7.813
1038
HND002 Hand, Foot and Mouth Disease 51 7.813
1039
TLR001 Tularemia 51 7.813
1040
P CHL066 Cholangitis 51 7.813
1041
HYP081 Hypolipoproteinemia 51 7.813
1042
RSP006 Respiratory System Disease 50 7.813
1043
c SVR005 Severe Pre-Eclampsia 50 7.813
1044
P MTR003 Mitral Valve Stenosis 50 7.813
1045
NPH010 Nephrosclerosis 50 7.813
1046
HYP080 Hypogonadism 50 7.813
1047
HYP017 Hypophosphatemia 50 7.813
1048
MCN001 Mucinous Adenocarcinoma 49 7.813
1049
VRC001 Varicocele 49 7.813
1050
c CNG389 Congenital Disorder of Glycosylation, Type Iim 49 7.813
1051
CLC006 Calcinosis 48 7.813
1052
RFR010 Refractory Anemia 48 7.813
1053
MSC077 Muscle Eye Brain Disease 47 7.813
1054
TST044 Testicular Torsion 47 7.813
1055
AND014 Androgenic Alopecia 46 7.813
1056
JNT004 Joint Laxity, Short Stature, and Myopia 45 7.813
1057
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 7.813
1058
SWN001 Swine Influenza 45 7.813
1059
APP009 Appendix Adenocarcinoma 44 7.813
1060
P BLP003 Blepharospasm 44 7.813
1061
MTR010 Mature Teratoma 44 7.813
1062
P TST026 Testicular Germ Cell Cancer 43 7.813