Search results for Guanosine triphosphate

1128 hits were found for Guanosine triphosphate

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 65 31.124
2
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 23.922
3
CHL014 Cholera 62 18.484
4
HMN044 Human Immunodeficiency Virus Type 1 78 14.615
5
P HRP006 Herpes Simplex 65 12.847
6
P NRB001 Neuroblastoma 66 12.689
7
IMP005 Impotence 52 12.121
8
IMM167 Immune Deficiency Disease 78 11.628
9
HLX001 Helix Syndrome 48 10.499
10
VCC001 Vaccinia 47 10.094
11
ISC004 Ischemia 61 9.974
12
P PLM037 Pulmonary Hypertension 72 9.810
13
c HPT001 Hepatitis C 62 9.731
14
c HPT073 Hepatitis C Virus 71 9.534
15
P PHC003 Pheochromocytoma 69 9.431
16
ADR040 Adrenal Gland Pheochromocytoma 46 9.413
17
HYP266 Hypoxia 57 9.280
18
P DYS154 Dystonia 64 8.871
19
ANX004 Anoxia 40 8.677
20
48X005 48,xyyy 39 8.414
21
P LKM002 Leukemia 67 8.230
22
GLM045 Glioma 63 8.122
23
GLL048 Glial Tumor 52 8.040
24
RPD005 Rapidly Involuting Congenital Hemangioma 46 7.792
25
STM007 Stomatitis 54 7.787
26
P LKM071 Leukemia, Chronic Lymphocytic 75 7.777
27
P LKM062 Leukemia, Acute Lymphoblastic 69 7.747
28
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 7.401
29
SPN186 Spinal Cord Injury 61 7.340
30
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 7.190
31
CYS001 Cystic Fibrosis 78 7.155
32
c LKM061 Leukemia, Acute Myeloid 83 7.111
33
TXC005 Toxic Shock Syndrome 62 7.013
34
CYT002 Cytokine Deficiency 43 6.999
35
AGN016 Aging 54 6.985
36
ACQ007 Acquired Immunodeficiency Syndrome 59 6.968
37
c PLM164 Pulmonary Hypertension, Primary, 1 76 6.802
38
P HPT021 Hepatitis 69 6.789
39
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 6.618
40
BRN071 Brain Injury 50 6.603
41
CRB004 Cerebral Artery Occlusion 45 6.543
42
P ALZ034 Alzheimer Disease 87 6.537
43
CHC001 Chickenpox 57 6.500
44
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 6.499
45
P GLM040 Glioma Susceptibility 1 71 6.445
46
47X002 47,xyy 48 6.335
47
P ATR011 Atrial Fibrillation 66 6.333
48
MLG169 Malignant Astrocytoma 57 6.324
49
GLB002 Glioblastoma 67 6.311
50
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 6.283
51
PRS045 Prostatic Hypertrophy 53 6.228
52
HYP066 Hyperglycemia 61 6.190
53
HYP060 Hyperinsulinism 54 6.179
54
P HPT023 Hepatocellular Carcinoma 96 6.160
55
P MYL006 Myeloid Leukemia 61 6.101
56
c PRC016 Pre-Eclampsia 65 6.092
57
c HPT016 Hepatitis B 62 5.972
58
TRM010 Traumatic Brain Injury 51 5.958
59
c ACT073 Acute Leukemia 58 5.936
60
OST159 Osteogenic Sarcoma 66 5.915
61
PRS021 Prostatic Adenoma 43 5.865
62
c MGR028 Migraine with or Without Aura 1 64 5.820
63
P LNG032 Lung Cancer 98 5.815
64
PRS129 Prostatic Hyperplasia, Benign 49 5.813
65
c TYP009 Type 2 Diabetes Mellitus 92 5.746
66
CLT003 Colitis 63 5.717
67
NRR001 Neuroretinitis 42 5.711
68
RTN023 Retinitis 46 5.711
69
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 5.707
70
P MYP004 Myopathy 67 5.650
71
P INF037 Inflammatory Bowel Disease 53 5.635
72
c MCR130 Microvascular Complications of Diabetes 6 41 5.556
73
c MCR120 Microvascular Complications of Diabetes 7 47 5.556
74
c MCR113 Microvascular Complications of Diabetes 3 52 5.556
75
c MCR133 Microvascular Complications of Diabetes 4 41 5.556
76
P HRT032 Heart Disease 81 5.554
77
HYP056 Hypoglycemia 65 5.484
78
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.417
79
c SML038 Small Cell Cancer of the Lung 69 5.416
80
HYP141 Hyperphenylalaninemia 42 5.411
81
DFC004 Deficiency Anemia 74 5.399
82
FTT001 Fatty Liver Disease 62 5.378
83
P BCL017 B-Cell Lymphoma 59 5.370
84
P GST053 Gastric Cancer 83 5.361
85
NNL005 Non-Alcoholic Fatty Liver Disease 63 5.339
86
P VSC007 Vascular Disease 63 5.321
87
c DLT002 Dilated Cardiomyopathy 78 5.318
88
BNR002 Bone Resorption Disease 47 5.317
89
c CHR684 Chronic Kidney Disease 69 5.254
90
PLM129 Pulmonary Disease, Chronic Obstructive 74 5.251
91
P ENC018 Encephalopathy 62 5.248
92
CNG034 Congestive Heart Failure 69 5.236
93
c HYP595 Hypertension, Essential 85 5.235
94
P OVR042 Ovarian Cancer 88 5.163
95
LVR012 Liver Cirrhosis 63 5.132
96
ANG054 Angina Pectoris 66 5.071
97
CHL068 Cholestasis 61 5.047
98
SVR001 Severe Acute Respiratory Syndrome 67 5.005
99
HMN014 Human Immunodeficiency Virus Infectious Disease 54 5.005
100
P HML002 Hemolytic Anemia 62 4.988
101
P SZR006 Seizure Disorder 70 4.986
102
P DBT009 Diabetes Mellitus 67 4.980
103
P CRD119 Cardiac Arrest 67 4.940
104
CRH001 Crohn's Disease 80 4.933
105
c ATR087 Atrial Standstill 1 74 4.933
106
c HYP836 Hypercholesterolemia, Familial, 1 73 4.925
107
P RTN008 Retinitis Pigmentosa 80 4.923
108
TTN003 Tetanus 65 4.894
109
P PRK039 Parkinsonism 55 4.869
110
MDD018 Middle East Respiratory Syndrome 44 4.861
111
P TRM003 Tremor 48 4.844
112
P MLN008 Melanoma 76 4.843
113
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 4.839
114
END086 End Stage Renal Disease 52 4.825
115
PPL052 Papillomatosis, Confluent and Reticulated 34 4.808
116
P LVR013 Liver Disease 69 4.804
117
ALL029 Allergic Disease 59 4.800
118
LWC001 Low Compliance Bladder 45 4.795
119
c ACT071 Acute Kidney Failure 60 4.764
120
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 4.760
121
P RTN016 Retinal Degeneration 52 4.746
122
MNT002 Mental Depression 57 4.742
123
SVR004 Severe Combined Immunodeficiency 72 4.731
124
BRN004 Brain Edema 54 4.729
125
DPR016 Depression 65 4.715
126
GTP002 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia 18 4.686
127
CRN030 Coronary Stenosis 50 4.680
128
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.659
129
c LKM005 Leukemia, T-Cell, Chronic 34 4.659
130
P MJR001 Major Depressive Disorder 68 4.634
131
P CHR345 Chronic Pain 50 4.615
132
P PNC035 Pancreatic Cancer 86 4.602
133
INS001 Insulinoma 59 4.585
134
LPP008 Lipoprotein Quantitative Trait Locus 65 4.565
135
ULC004 Ulcerative Colitis 74 4.531
136
P KDN018 Kidney Disease 72 4.495
137
P HNT016 Huntington Disease 73 4.446
138
P HYP265 Hypotonia 42 4.436
139
MDD011 Mood Disorder 62 4.371
140
ART140 Arteries, Anomalies of 53 4.366
141
P LCT001 Lactic Acidosis 51 4.357
142
GT001 Gout 64 4.336
143
P MSC005 Muscular Dystrophy 67 4.325
144
PLY150 Polykaryocytosis Inducer 29 4.297
145
P INF038 Influenza 68 4.228
146
PHN003 Phenylketonuria 76 4.219
147
P LNG064 Lung Cancer Susceptibility 3 70 4.208
148
P DNG005 Dengue Virus 56 4.203
149
P KLZ004 Kala-Azar 1 41 4.202
150
LSH001 Leishmaniasis 64 4.202
151
P NTR004 Neutropenia 63 4.201
152
LNG099 Lung Disease 62 4.192
153
P PRP019 Peripheral Nervous System Disease 58 4.190
154
c MCR115 Microvascular Complications of Diabetes 5 65 4.174
155
ATH013 Atherosclerosis Susceptibility 63 4.167
156
c BRN108 Branchiootic Syndrome 1 62 4.167
157
P MYC007 Myocardial Infarction 70 4.147
158
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.130
159
P LTR001 Lateral Sclerosis 58 4.130
160
HYP014 Hyperuricemia 51 4.112
161
c SYS001 Systemic Lupus Erythematosus 87 4.112
162
P BRS047 Breast Cancer 98 4.104
163
OCL069 Ocular Motor Apraxia 57 4.094
164
P NRP001 Neuropathy 60 4.088
165
PRT251 Proteinuria, Chronic Benign 57 4.086
166
P ADL010 Adult Respiratory Distress Syndrome 71 4.053
167
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 4.034
168
PRT013 Portal Hypertension 59 4.028
169
P NRF002 Neurofibromatosis 57 4.017
170
P SCK005 Sickle Cell Disease 56 4.015
171
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 4.009
172
SYN036 Syncope 45 4.007
173
P GLM007 Glomerulonephritis 60 3.979
174
c OPT053 Optic Atrophy 1 62 3.975
175
c LKM063 Leukemia, Chronic Myeloid 71 3.965
176
P LPS004 Lupus Erythematosus 61 3.962
177
P CYS018 Cystitis 59 3.958
178
LPD008 Lipid Metabolism Disorder 62 3.931
179
P CRN300 Coronary Heart Disease 1 73 3.931
180
P HYP076 Hyperthyroidism 53 3.927
181
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 3.920
182
RNL114 Renal Cell Carcinoma, Nonpapillary 80 3.902
183
CHL123 Chlamydia 58 3.880
184
P THR014 Thrombocytopenia 66 3.873
185
P INT143 Interstitial Cystitis 60 3.823
186
CHG001 Chagas Disease 66 3.820
187
HPT004 Hepatic Coma 43 3.788
188
P MLT020 Multiple Sclerosis 79 3.786
189
c MJR022 Major Affective Disorder 8 38 3.766
190
c MJR024 Major Affective Disorder 9 41 3.766
191
P BPL003 Bipolar Disorder 56 3.766
192
P AST005 Asthma 76 3.757
193
OVR094 Ovarian Epithelial Cancer 39 3.749
194
P INF032 Infertility 57 3.732
195
P OPT006 Optic Nerve Disease 58 3.720
196
P PRK057 Parkinson Disease, Late-Onset 80 3.704
197
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 3.704
198
MYC005 Myocardial Stunning 46 3.704
199
INS024 Insulin-Like Growth Factor I 78 3.702
200
HMP009 Haemophilus Influenzae 41 3.682
201
BCT022 Bacterial Infectious Disease 56 3.677
202
P EXN002 Exanthem 58 3.664
203
LSC001 Lesch-Nyhan Syndrome 62 3.624
204
ACT098 Acute Erythroid Leukemia 55 3.610
205
P CTN015 Cutaneous T Cell Lymphoma 48 3.605
206
CMB007 Combined Immunodeficiency 57 3.600
207
MSL001 Measles 61 3.588
208
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.571
209
P CLR023 Colorectal Cancer 100 3.558
210
NNL006 Non-Alcoholic Steatohepatitis 54 3.555
211
P RHN004 Rhinitis 57 3.550
212
P SKN015 Skin Carcinoma 71 3.544
213
MYL009 Myelodysplastic Syndrome 67 3.518
214
ATM095 Autoimmune Disease 61 3.517
215
P PRD008 Periodontitis 64 3.512
216
P OBS001 Obstructive Jaundice 48 3.472
217
P EPL164 Epilepsy 68 3.455
218
ADN001 Adenosine Deaminase Deficiency 59 3.453
219
P HYP098 Hypereosinophilic Syndrome 66 3.452
220
CLN015 Colon Adenocarcinoma 65 3.452
221
P ADN016 Adenocarcinoma 63 3.423
222
PNG002 Pain Agnosia 51 3.417
223
ATS010 Autosomal Recessive Disease 42 3.414
224
P RHM011 Rheumatoid Arthritis 82 3.405
226
SPL018 Splenomegaly 49 3.394
227
c TYP008 Type 1 Diabetes Mellitus 70 3.368
228
SQM006 Squamous Cell Carcinoma 60 3.367
229
HGH043 High Grade Glioma 45 3.364
230
P PSR002 Psoriasis 63 3.362
231
PST011 Pustulosis of Palm and Sole 52 3.362
232
CRT015 Carotid Artery Occlusion 45 3.333
233
P MLN007 Male Infertility 56 3.327
234
RNL077 Renal Fibrosis 46 3.326
235
P MYC008 Myocarditis 59 3.323
236
PRT036 Peritonitis 65 3.321
237
BRN024 Bronchitis 67 3.319
238
CNS004 Constipation 56 3.308
239
MLR004 Malaria 80 3.306
240
VLK001 Volkmann Contracture 23 3.299
241
DPH001 Diphtheria 59 3.292
242
URT010 Ureteral Obstruction 45 3.288
243
MTB004 Metabolic Acidosis 48 3.275
244
ADN018 Adenoma 59 3.273
245
BLR008 Bilirubin Metabolic Disorder 57 3.263
246
THR024 Thrombosis 56 3.258
247
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 3.248
248
PLM010 Pulmonary Edema 55 3.245
249
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 3.243
250
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 3.243
251
HPT019 Hepatic Encephalopathy 59 3.237
252
P NPH012 Nephrotic Syndrome 60 3.229
253
IRR002 Irritable Bowel Syndrome 65 3.222
254
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.216
255
c ACT027 Acute Pancreatitis 60 3.199
256
ALC007 Alcohol Dependence 66 3.195
257
c ACT134 Acute Liver Failure 59 3.184
258
SLP001 Sleeping Sickness 56 3.181
259
INT007 Intermediate Coronary Syndrome 54 3.159
260
HMN047 Human Cytomegalovirus Infection 57 3.146
261
HRW001 Hair Whorl 35 3.114
262
c ACT075 Acute Myocardial Infarction 56 3.111
263
ALL014 Allergic Encephalomyelitis 34 3.111
264
P MLG056 Malignant Hyperthermia 66 3.109
265
P BLD134 Bladder Cancer 79 3.100
266
CRV035 Cervical Cancer 73 3.100
267
STR067 Stroke, Ischemic 80 3.080
268
P BND020 Bone Disease 59 3.080
269
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 3.071
270
c VRL010 Viral Hepatitis 53 3.064
271
P SCH015 Schizophrenia 74 3.053
272
P MYC084 Mycobacterium Tuberculosis 1 68 3.048
273
P ECL001 Eclampsia 52 3.046
274
P GRF003 Graft-Versus-Host Disease 71 3.024
275
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.020
276
ARG004 Argyria 26 3.019
277
SXL003 Sexual Disorder 49 3.012
278
DMY004 Demyelinating Disease 50 3.005
279
LYM019 Lymphosarcoma 46 2.997
280
P PNC044 Pancreatitis 61 2.968
281
DBT010 Diabetic Neuropathy 54 2.968
282
P MTC133 Mitochondrial Myopathy 50 2.964
283
c PCH010 Pachyonychia Congenita 3 43 2.963
284
FBR047 Fibromyalgia 58 2.957
285
HRY003 Hairy Cell Leukemia 61 2.955
286
P MCR010 Microcephaly 60 2.955
287
P MVM001 Movement Disease 61 2.928
288
TRY001 Trypanosomiasis 50 2.928
289
MTH009 Mouth Disease 57 2.921
290
EXT007 Extracutaneous Mastocytoma 38 2.916
291
MST004 Mast Cell Neoplasm 42 2.916
292
P MSC003 Muscular Atrophy 52 2.911
293
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 2.907
294
TTR005 Tetrahydrobiopterin Deficiency 48 2.906
295
MTC005 Mitochondrial Metabolism Disease 45 2.906
296
P HDC001 Headache 57 2.892
297
CRB090 Cerebral Hypoxia 42 2.891
298
IRN002 Iron Metabolism Disease 57 2.889
299
P TTR001 Tetralogy of Fallot 69 2.885
300
MYL069 Myeloma, Multiple 77 2.878
301
P RTN024 Retinoblastoma 73 2.861
302
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.845
303
P NNT058 Neonatal Diabetes 52 2.844
304
P PLM036 Pulmonary Fibrosis 66 2.839
305
LYM027 Lymphopenia 56 2.835
306
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.834
307
P ENC004 Encephalitis 61 2.829
308
P BRB001 Beriberi 44 2.815
309
BRK010 Burkitt Lymphoma 66 2.813
310
SGW002 Segawa Syndrome, Autosomal Recessive 44 2.811
311
P LYM118 Lymphoma 67 2.809
312
P FBR017 Fibrosarcoma 56 2.805
313
DYS192 Dystonia, Dopa-Responsive 55 2.804
314
P ATX030 Ataxia-Telangiectasia 80 2.796
315
TLN003 Telangiectasis 51 2.796
316
SPN035 Spindle Cell Sarcoma 54 2.795
317
SRC014 Sarcoma 65 2.795
318
ESP021 Esophageal Cancer 83 2.782
319
P HRD217 Hereditary Optic Neuropathy 36 2.782
320
P HYP086 Hypothyroidism 69 2.757
321
ACT119 Acute Promyelocytic Leukemia 62 2.749
322
P BRS044 Breast Adenocarcinoma 58 2.727
323
LYM040 Lymphoblastic Lymphoma 53 2.713
324
GST033 Gestational Diabetes 61 2.708
325
P SLP006 Sleep Apnea 69 2.700
326
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.695
327
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.695
328
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.695
329
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.695
330
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.695
331
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.695
332
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.695
333
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.695
334
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.695
335
TRC003 Trichomoniasis 53 2.694
336
P ART022 Arthritis 71 2.693
337
MSC157 Muscular Dystrophy, Duchenne Type 79 2.690
338
P MTC069 Mitochondrial Disorders 57 2.678
339
P RSP003 Respiratory Failure 74 2.676
340
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.648
341
P HYP061 Hypertrophic Cardiomyopathy 69 2.642
342
PRP016 Paraplegia 52 2.615
343
END057 Endometrial Cancer 72 2.615
344
P CHN059 Chondrocalcinosis 52 2.614
345
P TMP001 Temporal Lobe Epilepsy 49 2.607
346
HRP004 Herpes Zoster 61 2.604
347
VRL011 Viral Infectious Disease 61 2.590
348
P ADL017 Adult T-Cell Leukemia 56 2.586
349
SKN016 Skin Disease 63 2.583
350
CHD001 Chediak-Higashi Syndrome 67 2.579
351
YLL002 Yellow Fever 61 2.575
352
P CNR004 Cone-Rod Dystrophy 2 74 2.572
353
ALL003 Allergic Rhinitis 67 2.567
354
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 2.562
355
CHR073 Choreatic Disease 54 2.562
356
P OLG002 Oligodendroglioma 66 2.559
357
GLC003 Glucose Intolerance 54 2.552
358
P URN019 Urinary Tract Infection 49 2.546
359
P VSC011 Vasculitis 61 2.534
360
ORL015 Oral Squamous Cell Carcinoma 43 2.529
361
THY029 Thyroid Carcinoma 51 2.529
362
OST012 Osteoarthritis 77 2.510
363
PTT037 Pituitary Tumors 44 2.504
364
P UVT001 Uveitis 57 2.502
365
P DRR001 Diarrhea 55 2.487
366
P GLL022 Guillain-Barre Syndrome 60 2.479
367
P BRN022 Bronchiectasis 60 2.469
368
P FLL037 Follicular Lymphoma 74 2.465
369
P CTR002 Cataract 60 2.463
370
P END044 Endometriosis 62 2.462
371
DSS032 Disease by Infectious Agent 55 2.462
372
ADR016 Adrenal Cortical Carcinoma 62 2.461
373
ADR054 Adrenocortical Carcinoma, Hereditary 47 2.461
374
ADR004 Adrenal Cortical Adenocarcinoma 38 2.461
375
P CHL066 Cholangitis 52 2.441
376
P BNG032 Benign Mesothelioma 53 2.430
377
P PRS040 Prostate Cancer 95 2.402
378
KRN002 Kearns-Sayre Syndrome 63 2.392
379
HMC014 Homocysteinemia 52 2.389
380
c SCL052 Scleroderma, Familial Progressive 61 2.374
381
CRB039 Cerebrovascular Disease 66 2.369
382
DGN001 Degenerative Disc Disease 49 2.368
383
URM002 Uremia 47 2.363
384
CRD132 Cardiac Conduction Defect 60 2.363
385
P GST044 Gastritis 55 2.360
386
PRM236 Primary Biliary Cholangitis 60 2.360
387
ANT024 Anthrax Disease 58 2.351
388
PST092 Posttransplant Acute Limbic Encephalitis 28 2.348
389
LMB062 Limb Ischemia 55 2.348
390
P SNS001 Sensorineural Hearing Loss 59 2.348
391
CHL004 Cholelithiasis 49 2.342
392
P RTN018 Retinal Disease 53 2.341
393
P MYP006 Myopia 56 2.335
394
ALL006 Allergic Asthma 56 2.325
395
BRN056 Bronchopulmonary Dysplasia 56 2.321
396
DWN001 Down Syndrome 70 2.315
397
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.307
398
P HYP069 Hyperparathyroidism 62 2.307
399
VSC003 Visceral Leishmaniasis 55 2.307
400
GST045 Gastroenteritis 58 2.304
401
P MNN013 Meningitis 65 2.287
402
c TBR025 Tuberous Sclerosis 1 84 2.277
403
RTN020 Retinal Vascular Disease 46 2.273
404
CLS049 Classic Phenylketonuria 41 2.261
405
c ATM011 Autoimmune Hepatitis 63 2.257
406
P CHR012 Chronic Granulomatous Disease 69 2.257
407
GNT003 Genital Herpes 54 2.253
408
P NSP012 Nasopharyngeal Carcinoma 61 2.242
409
P GRV001 Graves' Disease 55 2.223
410
RTN017 Retinal Detachment 60 2.213
411
KRT019 Keratitis, Hereditary 66 2.203
412
P ALP008 Alopecia 54 2.189
413
c CHR095 Chronic Progressive External Ophthalmoplegia 49 2.186
414
TRN015 Transient Cerebral Ischemia 63 2.182
415
P ART021 Arteriosclerosis 54 2.179
416
SKN019 Skin Melanoma 71 2.179
417
P SLP005 Sleep Disorder 61 2.175
418
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.153
419
c BCT007 Bacterial Meningitis 55 2.149
420
P CRD246 Cardiovascular System Disease 56 2.147
421
PLG002 Plague 58 2.146
422
CHL065 Cholangiocarcinoma 58 2.142
423
INT079 Intrahepatic Cholangiocarcinoma 51 2.142
424
XRD010 Xeroderma Pigmentosum, Variant Type 73 2.137
425
c GLL024 Gallbladder Disease 1 52 2.136
426
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 2.136
427
INT066 Interstitial Lung Disease 60 2.136
428
P SCK002 Sick Sinus Syndrome 55 2.130
429
P NNN008 Noonan Syndrome 1 77 2.126
430
P FML011 Familial Adenomatous Polyposis 71 2.125
431
MSC007 Muscle Hypertrophy 64 2.123
432
WLL004 Wallerian Degeneration 38 2.111
433
CRN019 Coronary Artery Vasospasm 47 2.109
434
RBS001 Rabies 58 2.105
435
HND015 Hand Skill, Relative 30 2.105
436
NRM005 Neuromuscular Disease 63 2.096
437
P LPR021 Leprosy 3 71 2.094
438
HNS001 Hansen's Disease 32 2.094
439
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 2.094
440
P MYS003 Myasthenia Gravis 68 2.085
441
c PSD047 Pseudo-Turner Syndrome 52 2.080
442
GRW007 Growth Hormone Deficiency 46 2.078
443
KRT009 Keratosis 53 2.076
444
CHR066 Chronic Fatigue Syndrome 60 2.074
445
GST040 Gastric Adenocarcinoma 67 2.063
446
P MYC033 Myoclonus 47 2.055
447
MST005 Mastitis 53 2.052
448
P EYD002 Eye Disease 57 2.052
449
P MTC010 Mitochondrial Dna Depletion Syndrome 47 2.051
450
P OVR082 Overgrowth Syndrome 49 2.048
451
ART016 Aortic Aneurysm 68 2.036
452
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.032
453
SCK003 Sickle Cell Anemia 74 2.032
454
c INH030 Inherited Retinal Disorder 28 2.032
455
STT001 Status Epilepticus 59 2.031
456
P HYP750 Hypertriglyceridemia, Familial 62 2.028
457
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 2.028
458
LYM017 Lyme Disease 62 2.027
459
MTB016 Metabolic Myopathy 30 2.025
460
MST020 Mast Cell Activation Syndrome 28 1.996
461
P TBR001 Tuberous Sclerosis 69 1.992
462
PTH003 Pathologic Nystagmus 52 1.991
463
P ESN008 Eosinophilic Pneumonia 50 1.984
464
HPT022 Hepatoblastoma 54 1.982
465
P DMN002 Dementia 66 1.981
466
P PTS002 Ptosis 52 1.981
467
P LMY004 Leiomyosarcoma 62 1.968
468
P KDN017 Kidney Cancer 61 1.965
469
MLD018 Mild Cognitive Impairment 48 1.964
470
MCS002 Mucositis 56 1.938
471
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.928
472
SCH014 Schistosomiasis 56 1.928
473
c HPT015 Hepatitis D 49 1.922
474
AZS001 Azoospermia 45 1.920
475
c THY107 Thymoma, Familial 42 1.917
476
P THY023 Thymoma 64 1.917
477
ANR040 Aneurysm 61 1.913
478
HYP264 Hypertonia 36 1.909
479
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.908
480
P DRM053 Dermatitis, Atopic 65 1.904
481
c ACT135 Acute Graft Versus Host Disease 51 1.896
482
P SPP010 Suppressor of Tumorigenicity 3 51 1.895
484
P ATT013 Attention Deficit-Hyperactivity Disorder 64 1.877
485
LWG006 Low Grade Glioma 41 1.872
486
P ESP024 Esophagitis 60 1.871
487
PRP030 Purpura 54 1.870
488
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.869
489
VRC001 Varicocele 48 1.869
490
GRN017 Granulocytopenia 42 1.869
491
CST001 Costello Syndrome 68 1.864
492
MRP001 Morphine Dependence 42 1.861
493
HDN002 Head Injury 44 1.857
494
MNT001 Mantle Cell Lymphoma 67 1.854
495
PPT005 Peptic Ulcer Disease 58 1.847
496
LGN006 Legionnaire Disease 52 1.838
497
PLS011 Plasmacytoma 56 1.838
498
P SRC025 Sarcoidosis 1 71 1.832
499
c ATS007 Autism Spectrum Disorder 72 1.828
500
DST006 Diastolic Heart Failure 45 1.824
501
WTH001 Withdrawal Disorder 48 1.824
502
CRB037 Cerebral Palsy 67 1.820
503
PRP027 Peripheral Vascular Disease 71 1.817
504
P MTR014 Motor Neuron Disease 65 1.816
505
NCL008 Nuclear Ribonucleic Acid 15 1.812
506
c FML001 Familial Atrial Fibrillation 65 1.807
507
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 1.806
508
BRN028 Brain Cancer 74 1.806
509
P SCL018 Scoliosis 57 1.804
510
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.793
511
MNN009 Meningoencephalitis 48 1.784
512
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.778
513
RCK004 Rickets 68 1.775
514
ACT003 Acute Kidney Tubular Necrosis 46 1.773
515
c RTN047 Retinitis Pigmentosa 18 46 1.767
516
HRT011 Heart Septal Defect 49 1.764
517
LNG039 Lung Squamous Cell Carcinoma 57 1.764
518
LSS003 Lassa Fever 49 1.763
519
PRP007 Priapism 47 1.762
520
P PRM011 Primary Ciliary Dyskinesia 69 1.759
521
WST005 West Nile Virus 57 1.759
522
SDD001 Sudden Infant Death Syndrome 60 1.758
523
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.758
524
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 56 1.756
525
THR004 Thrombocytosis 53 1.748
526
c HRD010 Hereditary Spastic Paraplegia 66 1.744
527
HRT012 Heart Valve Disease 53 1.743
528
GRY002 Gray Platelet Syndrome 58 1.743
529
CCC002 Coccidiosis 50 1.741
530
c SVR005 Severe Pre-Eclampsia 50 1.741
531
P ACT008 Actinic Keratosis 54 1.740
532
SCR003 Secretory Diarrhea 35 1.739
533
RYN005 Raynaud Phenomenon 45 1.739
534
DRM006 Dermatitis 62 1.738
535
P CRD224 Cardiofaciocutaneous Syndrome 1 71 1.736
536
MYL031 Myeloproliferative Neoplasm 66 1.726
537
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 1.726
538
P SLM003 Salmonellosis 54 1.725
539
PNC129 Pancreatic Adenocarcinoma 65 1.724
540
P ACN011 Acne 57 1.724
541
c GRV008 Graves Disease 1 54 1.718
542
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.698
543
P HYD006 Hydrocephalus 61 1.690
544
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.687
545
OBS002 Obsessive-Compulsive Disorder 68 1.687
546
NPH009 Nephrolithiasis 54 1.680
547
NWC001 Newcastle Disease 47 1.680
548
GLM044 Glomerular Disease 35 1.679
549
CHL067 Cholecystitis 60 1.674
550
P HRD011 Hereditary Spherocytosis 64 1.671
551
SLC006 Silicosis 56 1.670
552
c HMC039 Hemochromatosis, Type 1 73 1.668
553
P MLN069 Melanoma, Uveal 61 1.668
554
P OPN001 Open-Angle Glaucoma 55 1.668
555
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.655
556
CTN007 Cutaneous Leishmaniasis 62 1.655
557
MYL005 Myelofibrosis 71 1.653
558
CHK001 Chikungunya 60 1.646
559
IGR001 Ige Responsiveness, Atopic 59 1.646
560
c HPT003 Hepatitis a 63 1.646
561
P PMP001 Pemphigus 55 1.632
562
PST053 Postherpetic Neuralgia 40 1.632
563
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.628
564
P PTT006 Pituitary Adenoma 55 1.628
565
MSN001 Mesangial Proliferative Glomerulonephritis 44 1.624
566
P PRL003 Proliferative Glomerulonephritis 43 1.624
567
P WSK001 Wiskott-Aldrich Syndrome 72 1.618
568
c MST023 Mesothelioma, Malignant 56 1.614
569
P ANP001 Anaplastic Large Cell Lymphoma 61 1.614
570
P ART023 Arthropathy 61 1.614
571
P HMN010 Hemangioma 62 1.614
572
RTN003 Retinal Ischemia 49 1.599
573
GN1001 Gnao1 Encephalopathy 11 1.597
574
DWR001 Dwarfism 44 1.595
575
OCL006 Ocular Hypertension 53 1.595
576
PPL022 Papilloma 53 1.595
577
SQM002 Squamous Cell Papilloma 46 1.595
578
HMG002 Hemoglobinuria 50 1.593
579
NRL005 Neurilemmoma 60 1.593
580
P RHB003 Rhabdomyosarcoma 66 1.586
581
P VTR007 Vitreoretinopathy 46 1.585
582
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.585
583
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.585
584
CHR074 Choriocarcinoma 46 1.585
585
CYT005 Cytomegalovirus Retinitis 50 1.564
586
P RNV001 Renovascular Hypertension 49 1.559
587
CYN003 Cyanide Poisoning 22 1.558
588
TCK001 Tick-Borne Encephalitis 59 1.558
589
PRT058 Pure Autonomic Failure 58 1.558
590
c NRF024 Neurofibromatosis, Type I 72 1.554
591
P ART018 Aortic Valve Insufficiency 52 1.552
592
P HYP035 Hypophosphatasia 62 1.552
593
P NRN021 Neuronal Ceroid Lipofuscinosis 65 1.552
594
SFT003 Soft Tissue Sarcoma 57 1.552
595
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.550
596
RSP002 Respiratory Syncytial Virus Infectious Disease 52 1.550
597
BRN032 Brain Glioma 45 1.549
598
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 1.546
599
GST023 Gastric Ulcer 52 1.546
600
P PLY014 Polycystic Kidney Disease 69 1.545
601
KPS004 Kaposi Sarcoma 77 1.535
602
P AMY004 Amyloidosis 70 1.535
603
P FRG001 Fragile X Syndrome 70 1.528
604
P PRD021 Periodic Paralysis 41 1.510
606
HMP005 Hemiplegia 54 1.491
607
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.487
608
WST001 West Syndrome 59 1.487
609
c PRM005 Primary Hyperparathyroidism 59 1.487
610
P SPN046 Spinal Muscular Atrophy 63 1.486
611
TST014 Testicular Cancer 52 1.486
612
LKC009 Leukocyte Adhesion Deficiency, Type I 70 1.485
613
MCR013 Microphthalmia 60 1.485
614
ANX010 Anxiety 70 1.484
615
P MYT002 Myotonic Dystrophy 51 1.484
616
SQM013 Squamous Cell Carcinoma, Head and Neck 73 1.484
617
c SPR086 Spermatogenic Failure 3 46 1.484
618
P ALC033 Alcohol Use Disorder 61 1.484
619
c THR092 Thrombophilia Due to Thrombin Defect 74 1.474
620
HRN029 Hearing Loss, Noise-Induced 37 1.474
621
NRT004 Neuritis 53 1.474
622
P LNG028 Long Qt Syndrome 64 1.474
623
ADG002 Audiogenic Seizures 25 1.472
624
ASP004 Asphyxia Neonatorum 50 1.472
625
IDP070 Idiopathic Scoliosis 42 1.472
626
FND002 Fundus Dystrophy 55 1.471
627
P MGR001 Migraine Without Aura 49 1.471
628
MLG079 Malignant Pleural Mesothelioma 42 1.470
629
c ACT068 Acute Cystitis 61 1.469
630
P SYS005 Systemic Scleroderma 74 1.467
631
ORL011 Oral Cancer 60 1.467
632
LYM133 Lymphoma, Hodgkin, Classic 74 1.457
633
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.434
634
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.434
635
P STR022 Stargardt Disease 61 1.433
636
P PLY019 Polyneuropathy 52 1.433
637
OST003 Osteonecrosis 61 1.432
638
PYR010 Peyronie's Disease 50 1.418
639
STT041 Stuttering 52 1.418
640
P MTR012 Mitral Valve Disease 57 1.418
641
PLM035 Pulmonary Eosinophilia 49 1.418
642
P INS002 in Situ Carcinoma 53 1.418
643
P MCR129 Microvascular Complications of Diabetes 1 68 1.412
644
PNM008 Pneumothorax 54 1.412
645
c MCR112 Microvascular Complications of Diabetes 2 42 1.412
646
P OST002 Osteoporosis 76 1.410
647
P MDL005 Medulloblastoma 75 1.410
648
AVN001 Avian Influenza 61 1.410
649
c HRD198 Hereditary Dystonia 30 1.410
650
P PSD015 Pseudohypoparathyroidism 55 1.402
651
ILS001 Ileus 50 1.401
652
JPN002 Japanese Encephalitis 61 1.401
653
HYP080 Hypogonadism 50 1.401
654
ALB002 Albinism 47 1.401
655
P APL001 Aplastic Anemia 73 1.395
656
TRN018 Transitional Cell Carcinoma 56 1.389
657
P ATS364 Autism 69 1.386
658
P RRH023 Rare Hereditary Hemochromatosis 54 1.386
659
HMS001 Hemosiderosis 48 1.386
660
P SCL009 Sclerosing Cholangitis 48 1.386
661
P PLY011 Polycystic Ovary Syndrome 57 1.379
662
IGG001 Iga Glomerulonephritis 50 1.375
663
P ATR010 Atrial Heart Septal Defect 58 1.375
664
IRN001 Iron Deficiency Anemia 58 1.375
665
P OVR049 Ovarian Disease 52 1.375
666
c ACR088 Aicardi-Goutieres Syndrome 3 39 1.372
667
GST037 Gastroparesis 52 1.372
668
P DBT005 Diabetes Insipidus 54 1.367
669
CRV040 Cervix Carcinoma 50 1.358
670
JVN004 Juvenile Myelomonocytic Leukemia 67 1.341
671
PRM329 Premature Aging 36 1.338
672
P ICH004 Ichthyosis 56 1.338
673
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.329
674
ADN027 Adenomyosis 57 1.329
675
GTR002 Goiter 53 1.329
676
END041 Endometrial Adenocarcinoma 64 1.329
677
P CRB059 Cerebellar Degeneration 36 1.329
678
MCR088 Microscopic Polyangiitis 51 1.329
679
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.327
680
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.327
681
LPT014 Leptin Deficiency or Dysfunction 78 1.327
682
P MJR007 Major Affective Disorder 1 42 1.327
683
P MGR003 Migraine with Aura 52 1.327
684
EMB004 Embryonal Carcinoma 56 1.327
685
SYS003 Systolic Heart Failure 49 1.327
686
AMN003 Amnestic Disorder 54 1.327
687
PRP080 Peripheral Artery Disease 54 1.322
688
NRL016 Neural Tube Defects 81 1.322
689
c GLC092 Glaucoma, Primary Open Angle 62 1.322
690
P HRM001 Hermansky-Pudlak Syndrome 65 1.322
691
BLR001 Biliary Atresia 55 1.322
692
ATN004 Autonomic Neuropathy 42 1.322
693
MLD001 Melioidosis 67 1.322
694
ART002 Arts Syndrome 66 1.306
695
HLC007 Helicobacter Pylori Infection 67 1.306
696
c INH020 Inherited Metabolic Disorder 48 1.306
697
SPS057 Spasticity 42 1.303
698
INT002 Intermittent Claudication 61 1.303
699
P MYS005 Myositis 56 1.287
700
c CHL119 Cholangitis, Primary Sclerosing 58 1.287
701
TST044 Testicular Torsion 45 1.287
702
SNL007 Senile Cataract 40 1.281
703
BRN018 Borna Disease 36 1.261
704
P END033 Endocarditis 58 1.261
705
c HMN021 Human T-Cell Leukemia Virus Type 1 47 1.261
706
KRT002 Keratomalacia 55 1.254
707
P SPN301 Spinocerebellar Ataxia 2 59 1.246
708
CHL147 Chlamydia Pneumonia 47 1.246
709
P MTR003 Mitral Valve Stenosis 53 1.246
710
TRS021 Triosephosphate Isomerase Deficiency 45 1.246
711
GNT167 Genetic Obesity 30 1.244
712
LNN001 Lennox-Gastaut Syndrome 61 1.244
713
P FBR031 Febrile Seizures 52 1.244
714
P NRV007 Nervous System Disease 67 1.244
715
P RTT002 Rett Syndrome 79 1.242
716
c ART115 Aortic Valve Disease 1 74 1.234
717
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 1.234
718
P ALT001 Alternating Hemiplegia of Childhood 57 1.234
719
P ATR005 Atrophic Gastritis 50 1.234
720
ENT004 Enthesopathy 51 1.234
721
CHR178 Chromosomal Triplication 34 1.234
722
SPS019 Spastic Paraparesis 38 1.233
723
CRC021 Carcinosarcoma 64 1.233
724
MTR002 Mitral Valve Insufficiency 52 1.233
725
FBR054 Fibroma 44 1.230
726
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.230
727
P NRC002 Narcolepsy 56 1.230
728
P PRN023 Prion Disease 60 1.230
729
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.227
730
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.227
731
PLM033 Pulmonary Embolism 58 1.223
732
P LYM033 Lymphoproliferative Syndrome 59 1.212
733
FDL002 Food Allergy 47 1.212
734
GST050 Gastrointestinal System Disease 55 1.212
735
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 1.195
736
c CHR711 Chronic Asthma 41 1.195
737
MNK002 Monkeypox 41 1.195
738
TTH006 Tooth Disease 51 1.195
739
HYP006 Hypertensive Heart Disease 49 1.195
740
P TRC031 Trichorhinophalangeal Syndrome 38 1.195
741
P CRB088 Cerebral Atrophy 33 1.195
742
P XRD029 Xeroderma Pigmentosum, Complementation Group a 56 1.177
743
P MTH008 Methylmalonic Acidemia 52 1.177
744
PST028 Post-Traumatic Stress Disorder 59 1.177
745
ACT200 Acute Monoblastic Leukemia 41 1.177
746
c VRL012 Viral Meningitis 46 1.173
747
GRD001 Giardiasis 46 1.173
748
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 29 1.161
749
MNG007 Manganese Poisoning 28 1.161
750
ALC009 Alcoholic Liver Cirrhosis 54 1.161
751
ACL001 Acalculous Cholecystitis 38 1.161
752
c INF023 Inflammatory Breast Carcinoma 49 1.161
753
PNC060 Punctate Porokeratosis 28 1.161
754
c PSD108 Pseudohypoparathyroidism, Type Ia 65 1.149
755
OTT002 Otitis Media 71 1.149
756
FCL022 Focal Dystonia 42 1.149
757
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 56 1.149
758
EPL131 Epilepsy, Pyridoxine-Dependent 45 1.149
759
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.149
760
P VNT002 Ventricular Septal Defect 58 1.149
761
P MMB011 Membranous Nephropathy 50 1.149
762
c BPL002 Bipolar I Disorder 47 1.149
763
OPT003 Opiate Dependence 49 1.149
764
BRS051 Breast Disease 58 1.149
765
NRF007 Neurofibroma 64 1.149
766
ATN005 Autonomic Dysfunction 46 1.149
767
FRN006 Frontotemporal Dementia 68 1.144
768
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.144
769
c WLM013 Wilms Tumor 1 66 1.144
770
MCL006 Macular Retinal Edema 57 1.144
771
PPL002 Papillary Carcinoma 46 1.144
772
RSP007 Respiratory Distress Syndrome, Infant 40 1.123
773
CHR100 Chronic Ulcer of Skin 57 1.121
774
c ATM099 Autoimmune Uveitis 45 1.121
775
LRN003 Learning Disability 49 1.121
776
P CHR071 Charcot-Marie-Tooth Disease 64 1.121
777
BRC012 Brucellosis 66 1.121
778
c HPT007 Hepatitis E 51 1.121
779
BRK012 Broken Heart Syndrome 42 1.121
780
c BRS111 Breast-Ovarian Cancer, Familial 2 53 1.116
781
PNC001 Pancytopenia 53 1.116
782
SNS003 Sensory Peripheral Neuropathy 52 1.116
783
P DDN001 Duodenal Ulcer 53 1.116
784
P MYG005 Myoglobinuria 40 1.116
786
SDD008 Sudden Sensorineural Hearing Loss 41 1.100
787
c ANM038 Anemia, Autoimmune Hemolytic 64 1.100
788
c HYP292 Hypophosphatasia, Infantile 55 1.100
789
DGR001 Digeorge Syndrome 62 1.100
790
HPT067 Hepatocellular Adenoma 43 1.100
791
SMT008 Smith-Magenis Syndrome 54 1.098
792
P CND005 Cone Dystrophy 47 1.098
793
P CRG003 Crigler-Najjar Syndrome, Type I 63 1.098
794
c CNG411 Congenital Disorder of Glycosylation, Type in 67 1.098
795
LBR036 Leber Plus Disease 66 1.098
796
ACH005 Achalasia 55 1.098
797
P ACT105 Acute Mountain Sickness 52 1.098
798
NSP002 Nasopharyngitis 45 1.083
799
P FML023 Familial Hemiplegic Migraine 53 1.050
800
P PLY006 Polydactyly 59 1.050
801
c SPN294 Spinocerebellar Ataxia 1 53 1.050
802
PRS047 Prostatitis 58 1.050
803
DYS015 Dysentery 50 1.050
804
P KRN004 Kernicterus 46 1.050
805
NPH010 Nephrosclerosis 50 1.050
806
PLR005 Pleuropneumonia 33 1.050
807
BCT021 Bacterial Sepsis 43 1.049
808
P DRM010 Dermatomyositis 61 1.049
809
CRY005 Cryptococcosis 60 1.049
810
DNT012 Dental Caries 53 1.049
811
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 1.049
812
P PYL005 Pyelonephritis 57 1.049
813
P PGT001 Paget's Disease of Bone 61 1.049
814
P ART005 Arteriovenous Malformation 65 1.049
815
P BNC003 Bone Cancer 58 1.049
816
c CHR417 Chronic Graft Versus Host Disease 55 1.049
817
EPD015 Epidemic Typhus 44 1.046
818
CLP005 Ciliopathy 41 1.038
819
MSC152 Muscular Dystrophy, Becker Type 69 1.038
820
CLF027 Cleft Palate, Isolated 64 1.038
821
P CLC063 Celiac Disease 1 66 1.038
822
CRV043 Cervical Dystonia 46 1.038
823
P HRD021 Hereditary Sensory Neuropathy 48 1.038
824
ZLL002 Zollinger-Ellison Syndrome 55 1.038
825
URL001 Urolithiasis 46 1.038
826
c SCH079 Schizophrenia 1 44 1.038
827
VRC005 Varicose Veins 60 1.038
828
CLB010 Coloboma of Macula 53 1.038
829
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.038
830
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 1.038
831
P HML001 Hemolytic-Uremic Syndrome 52 1.038
832
OBS082 Obstructive Nephropathy 41 1.038
833
CWP001 Cowpox 45 1.038
834
PLM001 Pulmonary Tuberculosis 69 1.038
835
P CCK001 Cockayne Syndrome 68 1.038
836
P RTN014 Retinal Artery Occlusion 47 1.038
837
BRN026 Branch Retinal Artery Occlusion 41 1.038
838
P MTH007 Methemoglobinemia 46 1.038
839
FLR002 Filariasis 55 1.038
840
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 1.038
841
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 1.015
842
P RNL015 Renal Hypertension 45 1.015
843
c CNT035 Central Nervous System Disease 54 1.015
845
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 1.015
846
P FML018 Familial Mediterranean Fever 73 0.975
847
HYP457 Hypertrophic Scars 42 0.975
848
LNG108 Langerhans Cell Histiocytosis 58 0.975
849
ENT011 Enterocolitis 55 0.975
850
DNT005 Dentatorubral-Pallidoluysian Atrophy 60 0.975
851
OST017 Osteomyelitis 63 0.975
852
NPH003 Nephrocalcinosis 49 0.975
853
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 0.975
854
CRV002 Cervix Uteri Carcinoma in Situ 47 0.975
855
HST010 Histiocytosis 49 0.975
856
P CND004 Candidiasis 58 0.975
857
ACT084 Acute Stress Disorder 54 0.975
859
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.975
860
PSY004 Psychotic Disorder 66 0.975
861
P SBS003 Substance Abuse 54 0.975
862
P PRP029 Porphyria 60 0.975
863
LCH001 Leech Infestation 38 0.975
864
VSC002 Vascular Dementia 60 0.975
865
CRV045 Cervical Intraepithelial Neoplasia 39 0.975
866
PRN019 Perinatal Necrotizing Enterocolitis 60 0.975
867
NRT001 Neurotic Disorder 56 0.950
868
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.938
869
P SJG008 Sjogren Syndrome 61 0.938
870
P LSS002 Lissencephaly 50 0.938
871
PRP036 Peripheral T-Cell Lymphoma 53 0.938
872
c SVR003 Severe Congenital Neutropenia 59 0.938
873
c ATM024 Autoimmune Pancreatitis 52 0.938
874
TRD006 Tardive Dyskinesia 53 0.938
875
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.938
876
GBT001 Gaba-Transaminase Deficiency 37 0.938
877
c ACR091 Aicardi-Goutieres Syndrome 4 35 0.938
878
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.938
879
c HYP368 Hyperphenylalaninemia, Bh4-Deficient, C 37 0.938
880
URT049 Urate Oxidase, Pseudogene 24 0.938
881
PLT016 Platelet Adenylate Cyclase Activity 16 0.938
882
CRR012 Cirrhotic Cardiomyopathy 22 0.938
883
P GRS003 Griscelli Syndrome 53 0.938
884
GST030 Gastrinoma 45 0.938
885
P FCL005 Focal Segmental Glomerulosclerosis 57 0.938
886
RTR008 Root Resorption 44 0.938
887
P INT068 Intestinal Disease 53 0.938
888
CCN002 Cocaine Abuse 49 0.938
889
P TCD001 Tic Disorder 49 0.938
890
CRT004 Carotid Artery Thrombosis 39 0.938
891
TBL023 Tubulinopathies 31 0.938
892
DYS073 Dysphagia 53 0.938
893
CRC006 Carcinoid Syndrome 55 0.938
894
WBR001 Weber Syndrome 38 0.921
895
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 61 0.921
896
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.921
897
c LBR004 Leber Congenital Amaurosis 1 52 0.921
898
HYP114 Hypertensive Nephropathy 36 0.921
899
P JBR020 Joubert Syndrome 1 74 0.921
900
NVS017 Nevus, Epidermal 66 0.921
901
PNC013 Pancreatic Ductal Carcinoma 48 0.921
902
CRN017 Coronary Thrombosis 46 0.921
903
P ANG015 Angioedema 56 0.921
904
c MLG069 Malignant Hypertension 46 0.921
905
CLN019 Colonic Disease 47 0.921
906
ANC002 Anca-Associated Vasculitis 44 0.921
907
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.892
908
c PNS012 Paine Syndrome 60 0.892
909
RTC012 Reticuloendotheliosis, X-Linked 35 0.892
910
MND023 Mend Syndrome 49 0.892
911
BRT054 Brittle Bone Disorder 74 0.892
912
c EXD008 Exudative Vitreoretinopathy 1 71 0.892
913
P OCL002 Oculocutaneous Albinism 59 0.892
914
HMR023 Hemorrhagic Cystitis 43 0.892
915
INF034 Infective Endocarditis 54 0.892
916
CRH005 Crohn's Colitis 53 0.892
917
P SML001 Small Cell Carcinoma 52 0.892
918
WRN001 Werner Syndrome 69 0.892
919
c DVL062 Developmental and Epileptic Encephalopathy 35 29 0.892
920
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.892
921
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.892
922
CHL149 Childhood Acute Myeloid Leukemia 43 0.892
923
P FBR003 Fibrous Histiocytoma 43 0.892
924
P HMC002 Homocystinuria 53 0.892
925
CLF001 Cleft Lip 53 0.892
926
c BCT013 Bacterial Pneumonia 48 0.892
927
TRT001 Teratocarcinoma 42 0.892
928
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.892
929
EXT034 Extrinsic Allergic Alveolitis 57 0.892
930
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.892
931
CMM004 Common Variable Immunodeficiency 72 0.892
932
FLR001 Filarial Elephantiasis 59 0.892
933
c MLG084 Malignant Fibrous Histiocytoma 62 0.892
934
P GCH001 Gaucher's Disease 70 0.892
935
CYS014 Cystadenocarcinoma 51 0.892
936
PRM013 Premature Menopause