Search results for Cytidine triphosphate

701 hits were found for Cytidine triphosphate

# Family MCID Name MIFTS Score
1
HMN044 Human Immunodeficiency Virus Type 1 76 9.656
2
IMM167 Immune Deficiency Disease 76 7.183
3
PRT037 Pertussis 49 6.730
4
c LKM061 Leukemia, Acute Myeloid 83 5.965
5
P LKM002 Leukemia 65 5.575
6
P LKM071 Leukemia, Chronic Lymphocytic 74 5.323
7
P HRP006 Herpes Simplex 65 5.317
8
P LKM062 Leukemia, Acute Lymphoblastic 69 5.089
9
MYL009 Myelodysplastic Syndrome 67 5.053
10
P BCL017 B-Cell Lymphoma 57 4.859
11
P LNG032 Lung Cancer 98 4.765
12
P NRB001 Neuroblastoma 66 4.689
13
c HPT001 Hepatitis C 61 4.616
14
END040 Endogenous Depression 54 4.516
15
ISC004 Ischemia 61 4.500
16
c HPT073 Hepatitis C Virus 70 4.459
17
MNT002 Mental Depression 56 4.321
18
DPR016 Depression 64 4.313
19
P PNC035 Pancreatic Cancer 87 4.304
20
P HPT021 Hepatitis 68 4.260
21
VCC001 Vaccinia 49 4.237
22
c SML038 Small Cell Cancer of the Lung 68 4.219
23
c HPT016 Hepatitis B 62 4.217
24
HLX001 Helix Syndrome 47 4.179
25
P MYL006 Myeloid Leukemia 60 4.094
26
c MJR022 Major Affective Disorder 8 37 4.059
27
c MJR024 Major Affective Disorder 9 40 4.059
28
P BPL003 Bipolar Disorder 56 4.059
29
c ACT073 Acute Leukemia 59 4.024
30
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.916
31
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.906
32
BRK010 Burkitt Lymphoma 65 3.860
33
CHL014 Cholera 62 3.849
34
P LYM118 Lymphoma 66 3.838
35
HYP266 Hypoxia 56 3.812
36
P FLL037 Follicular Lymphoma 66 3.729
37
P HPT023 Hepatocellular Carcinoma 95 3.666
38
RPD005 Rapidly Involuting Congenital Hemangioma 48 3.584
39
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.535
40
ANX004 Anoxia 40 3.412
41
NRT001 Neurotic Disorder 56 3.406
42
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 3.374
43
48X005 48,xyyy 39 3.351
44
P NTR004 Neutropenia 62 3.281
45
P HML002 Hemolytic Anemia 62 3.216
46
P PHC003 Pheochromocytoma 70 3.206
47
ADR040 Adrenal Gland Pheochromocytoma 45 3.202
48
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 3.165
49
c LKM005 Leukemia, T-Cell, Chronic 33 3.165
50
CYS001 Cystic Fibrosis 77 3.159
51
GLB002 Glioblastoma 67 3.092
52
STM007 Stomatitis 52 3.056
53
ACQ007 Acquired Immunodeficiency Syndrome 58 3.049
54
AGN016 Aging 53 3.036
55
CLT003 Colitis 63 3.031
56
P MJR007 Major Affective Disorder 1 42 2.885
57
P INF038 Influenza 68 2.869
58
P INF037 Inflammatory Bowel Disease 53 2.847
59
P OVR042 Ovarian Cancer 88 2.837
60
BRN071 Brain Injury 50 2.825
61
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.824
62
P ALZ034 Alzheimer Disease 87 2.823
63
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.792
64
P GST053 Gastric Cancer 82 2.762
65
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.741
66
P MYP004 Myopathy 67 2.705
67
PNC129 Pancreatic Adenocarcinoma 64 2.695
68
RHB024 Rhabdomyosarcoma 2 65 2.685
69
ATM095 Autoimmune Disease 61 2.620
70
P DBT009 Diabetes Mellitus 67 2.582
71
CRB039 Cerebrovascular Disease 65 2.539
72
NRR001 Neuroretinitis 42 2.527
73
RTN023 Retinitis 45 2.527
74
P LVR013 Liver Disease 68 2.526
75
P BRS047 Breast Cancer 97 2.525
76
CYT002 Cytokine Deficiency 43 2.513
77
P OPT006 Optic Nerve Disease 57 2.509
78
P MSC005 Muscular Dystrophy 66 2.493
79
P NRP001 Neuropathy 59 2.486
80
c SYS001 Systemic Lupus Erythematosus 85 2.423
81
DFF005 Diffuse Large B-Cell Lymphoma 55 2.421
82
ALL029 Allergic Disease 61 2.415
83
HYP005 Hypokalemia 55 2.313
84
HYP066 Hyperglycemia 60 2.306
85
GLM045 Glioma 62 2.302
86
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 2.301
87
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.301
88
DFC004 Deficiency Anemia 74 2.291
89
GLL048 Glial Tumor 51 2.291
90
TRM010 Traumatic Brain Injury 50 2.284
91
SQM006 Squamous Cell Carcinoma 59 2.273
92
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.259
93
SVR004 Severe Combined Immunodeficiency 70 2.255
94
CRH001 Crohn's Disease 80 2.245
95
P LNG064 Lung Cancer Susceptibility 3 69 2.233
96
c TYP008 Type 1 Diabetes Mellitus 77 2.226
97
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.199
98
ULC004 Ulcerative Colitis 74 2.184
99
P CRD119 Cardiac Arrest 68 2.181
100
P TRN020 Turner Syndrome 67 2.168
101
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 2.164
102
VRL011 Viral Infectious Disease 60 2.158
103
P INF032 Infertility 60 2.151
104
P ADN016 Adenocarcinoma 63 2.148
105
ORL015 Oral Squamous Cell Carcinoma 43 2.130
106
END086 End Stage Renal Disease 54 2.126
107
OCL069 Ocular Motor Apraxia 57 2.113
108
HMP009 Haemophilus Influenzae 41 2.107
109
FTT001 Fatty Liver Disease 61 2.103
110
P MJR001 Major Depressive Disorder 68 2.097
111
P LPS004 Lupus Erythematosus 61 2.096
112
P MLN008 Melanoma 75 2.093
113
P ATX030 Ataxia-Telangiectasia 80 2.092
114
TLN003 Telangiectasis 51 2.092
115
P GLM040 Glioma Susceptibility 1 70 2.083
116
P FBR017 Fibrosarcoma 55 2.079
117
P BLD134 Bladder Cancer 79 2.075
118
c ACT071 Acute Kidney Failure 60 2.070
119
TXC005 Toxic Shock Syndrome 61 2.070
120
MLG169 Malignant Astrocytoma 57 2.070
121
47X002 47,xyy 47 2.064
122
ARG004 Argyria 26 2.058
123
OST159 Osteogenic Sarcoma 66 2.016
124
c BRN108 Branchiootic Syndrome 1 63 2.013
125
P EXN002 Exanthem 58 2.008
126
P PNM007 Pneumonia 64 2.004
127
BRN004 Brain Edema 54 1.978
128
CMB007 Combined Immunodeficiency 56 1.975
129
P GST044 Gastritis 55 1.961
130
ANT039 Antisynthetase Syndrome 55 1.952
131
P KLZ004 Kala-Azar 1 41 1.945
132
LSH001 Leishmaniasis 63 1.945
133
P THR014 Thrombocytopenia 66 1.938
134
HYP056 Hypoglycemia 65 1.929
135
c MCR115 Microvascular Complications of Diabetes 5 65 1.923
136
PPL052 Papillomatosis, Confluent and Reticulated 34 1.922
137
P ADL017 Adult T-Cell Leukemia 53 1.922
138
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.921
139
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.919
140
c HPT015 Hepatitis D 49 1.910
141
CHL065 Cholangiocarcinoma 57 1.904
142
INT079 Intrahepatic Cholangiocarcinoma 51 1.904
143
P AST005 Asthma 75 1.904
144
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.904
145
LYM143 Lymphoma, Non-Hodgkin, Familial 74 1.899
146
CHL068 Cholestasis 61 1.894
147
P RHM011 Rheumatoid Arthritis 81 1.892
148
SPN186 Spinal Cord Injury 60 1.889
149
P CLR023 Colorectal Cancer 100 1.879
150
P CHR285 Chronic Myelomonocytic Leukemia 59 1.870
151
ALL014 Allergic Encephalomyelitis 34 1.861
152
OVR094 Ovarian Epithelial Cancer 39 1.839
153
c ACT027 Acute Pancreatitis 60 1.829
154
SKN019 Skin Melanoma 70 1.827
155
CRB004 Cerebral Artery Occlusion 45 1.822
156
LNG099 Lung Disease 62 1.821
157
ESP021 Esophageal Cancer 84 1.816
158
P CHN059 Chondrocalcinosis 51 1.812
159
MDD011 Mood Disorder 61 1.811
160
P NSP012 Nasopharyngeal Carcinoma 60 1.809
161
BCT022 Bacterial Infectious Disease 55 1.808
162
PHN003 Phenylketonuria 76 1.797
163
c LKM063 Leukemia, Chronic Myeloid 70 1.794
164
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.791
165
GST045 Gastroenteritis 58 1.791
166
DWN001 Down Syndrome 70 1.780
167
LYM133 Lymphoma, Hodgkin, Classic 69 1.777
168
ACT098 Acute Erythroid Leukemia 55 1.758
169
P MLN007 Male Infertility 56 1.757
170
P MYC084 Mycobacterium Tuberculosis 1 68 1.756
171
P VSC011 Vasculitis 61 1.751
172
SPP007 Suppression Amblyopia 38 1.750
173
AMB002 Amblyopia 49 1.750
174
ALC007 Alcohol Dependence 65 1.748
175
CHL123 Chlamydia 58 1.741
176
c HYP836 Hypercholesterolemia, Familial, 1 73 1.740
177
CHG001 Chagas Disease 65 1.727
178
HMN047 Human Cytomegalovirus Infection 59 1.713
179
c PCH010 Pachyonychia Congenita 3 43 1.712
180
c PRC016 Pre-Eclampsia 64 1.709
181
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.704
182
HRY003 Hairy Cell Leukemia 53 1.695
183
MYL069 Myeloma, Multiple 76 1.687
184
MNT001 Mantle Cell Lymphoma 65 1.682
185
SVR001 Severe Acute Respiratory Syndrome 68 1.645
186
P ANR048 Aniridia 1 66 1.642
187
OST012 Osteoarthritis 77 1.634
188
P OPN001 Open-Angle Glaucoma 55 1.634
189
P PRK039 Parkinsonism 55 1.632
190
P MNC007 Monocytic Leukemia 48 1.632
191
MSC157 Muscular Dystrophy, Duchenne Type 78 1.631
192
CRV035 Cervical Cancer 72 1.628
193
ADN018 Adenoma 58 1.624
194
c TYP009 Type 2 Diabetes Mellitus 91 1.612
195
LVR012 Liver Cirrhosis 62 1.611
196
CHC001 Chickenpox 56 1.610
197
P KDN018 Kidney Disease 71 1.607
198
LYM019 Lymphosarcoma 46 1.603
199
HLC007 Helicobacter Pylori Infection 67 1.593
200
XRD010 Xeroderma Pigmentosum, Variant Type 72 1.593
201
TTN003 Tetanus 64 1.588
202
MSL001 Measles 61 1.587
203
ADN001 Adenosine Deaminase Deficiency 59 1.585
204
c ATR087 Atrial Standstill 1 74 1.583
205
P GLM007 Glomerulonephritis 59 1.579
206
c ATM011 Autoimmune Hepatitis 62 1.571
207
SPL018 Splenomegaly 47 1.569
208
ATH013 Atherosclerosis Susceptibility 63 1.559
209
P PLM037 Pulmonary Hypertension 69 1.559
210
P PNC044 Pancreatitis 61 1.547
211
MYC005 Myocardial Stunning 45 1.541
212
PRS129 Prostatic Hyperplasia, Benign 48 1.529
213
P ENC018 Encephalopathy 62 1.528
214
c CHR684 Chronic Kidney Disease 73 1.524
215
P RTN008 Retinitis Pigmentosa 79 1.514
216
c VRL010 Viral Hepatitis 52 1.511
217
PRS045 Prostatic Hypertrophy 53 1.510
218
GT001 Gout 63 1.507
219
c DLT002 Dilated Cardiomyopathy 79 1.500
220
P HRT032 Heart Disease 84 1.500
221
P SKN015 Skin Carcinoma 71 1.495
222
PRS021 Prostatic Adenoma 43 1.492
223
PLG002 Plague 58 1.484
224
GRN017 Granulocytopenia 42 1.484
225
P DNG005 Dengue Virus 55 1.478
226
SKN016 Skin Disease 63 1.469
227
KPS004 Kaposi Sarcoma 76 1.468
228
BLM001 Bloom Syndrome 65 1.454
229
P CRN300 Coronary Heart Disease 1 73 1.447
230
P SBS003 Substance Abuse 54 1.443
231
P PRD008 Periodontitis 63 1.437
232
ALL006 Allergic Asthma 55 1.429
233
P RTN024 Retinoblastoma 72 1.429
234
CCN001 Cocaine Dependence 47 1.425
235
P HYP076 Hyperthyroidism 53 1.420
236
BNR002 Bone Resorption Disease 47 1.420
237
P CHL066 Cholangitis 51 1.412
238
c HMN021 Human T-Cell Leukemia Virus Type 1 46 1.412
239
NCL008 Nuclear Ribonucleic Acid 15 1.410
240
HPT004 Hepatic Coma 43 1.410
241
MLR004 Malaria 77 1.403
242
SLP001 Sleeping Sickness 56 1.400
243
SPN035 Spindle Cell Sarcoma 51 1.389
244
SRC014 Sarcoma 64 1.389
245
KRT002 Keratomalacia 54 1.378
246
P PRP019 Peripheral Nervous System Disease 57 1.378
247
c GLC092 Glaucoma, Primary Open Angle 60 1.363
248
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 1.359
249
P TRM003 Tremor 50 1.357
250
CMM004 Common Variable Immunodeficiency 71 1.347
251
P BRN022 Bronchiectasis 59 1.346
252
SYN007 Synovitis 54 1.344
253
PLC002 Plica Syndrome 35 1.344
254
P NRF002 Neurofibromatosis 60 1.336
255
ORL011 Oral Cancer 60 1.318
256
KRT019 Keratitis, Hereditary 66 1.311
257
c ACT134 Acute Liver Failure 57 1.308
258
P CNR004 Cone-Rod Dystrophy 2 74 1.300
259
PLY150 Polykaryocytosis Inducer 29 1.293
260
P ENC004 Encephalitis 61 1.292
261
c MCR133 Microvascular Complications of Diabetes 4 41 1.289
262
c MCR113 Microvascular Complications of Diabetes 3 52 1.289
263
c MCR130 Microvascular Complications of Diabetes 6 41 1.289
264
c MCR120 Microvascular Complications of Diabetes 7 47 1.289
266
P HYP098 Hypereosinophilic Syndrome 66 1.277
267
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.273
268
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.268
269
LYM040 Lymphoblastic Lymphoma 53 1.268
270
MSC007 Muscle Hypertrophy 64 1.262
271
P ART023 Arthropathy 59 1.262
272
P UVT001 Uveitis 57 1.261
273
P SPP010 Suppressor of Tumorigenicity 3 50 1.258
274
P BRS044 Breast Adenocarcinoma 58 1.250
275
P SCH015 Schizophrenia 74 1.248
276
LPD008 Lipid Metabolism Disorder 61 1.237
277
CRT015 Carotid Artery Occlusion 45 1.232
278
VTM002 Vitamin B12 Deficiency 48 1.229
279
VSC002 Vascular Dementia 59 1.228
280
P URN019 Urinary Tract Infection 48 1.226
281
PLS011 Plasmacytoma 56 1.221
282
ACT119 Acute Promyelocytic Leukemia 62 1.217
283
P GRV001 Graves' Disease 54 1.215
284
CD4003 Cd40 Ligand Deficiency 53 1.207
285
VSC003 Visceral Leishmaniasis 54 1.205
286
RCK004 Rickets 64 1.203
287
BLR008 Bilirubin Metabolic Disorder 57 1.202
288
NNL006 Non-Alcoholic Steatohepatitis 54 1.191
289
c SPN225 Spondyloarthropathy 1 70 1.191
290
SPN051 Spondylitis 51 1.191
291
INF009 Inflammatory Spondylopathy 30 1.191
292
BCK006 Back Pain 43 1.191
293
P MSC003 Muscular Atrophy 52 1.187
294
P PRK057 Parkinson Disease, Late-Onset 79 1.184
295
P MTC069 Mitochondrial Disorders 57 1.184
296
P VSC007 Vascular Disease 62 1.181
297
PLC007 Placental Abruption 47 1.176
298
PRT036 Peritonitis 65 1.170
299
P MLT020 Multiple Sclerosis 79 1.164
300
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.155
301
P LTR001 Lateral Sclerosis 57 1.155
302
FDL002 Food Allergy 47 1.151
303
P HNT016 Huntington Disease 73 1.149
304
PRT251 Proteinuria, Chronic Benign 58 1.127
305
P ALP008 Alopecia 53 1.124
306
P TMP003 Temporal Arteritis 68 1.121
307
SLD003 Sialadenitis 47 1.121
308
THY029 Thyroid Carcinoma 55 1.119
309
P SRC025 Sarcoidosis 1 70 1.112
310
ACT250 Acute Megakaryocytic Leukemia 63 1.100
311
MDD018 Middle East Respiratory Syndrome 44 1.100
312
P ECL001 Eclampsia 52 1.098
313
P HYP061 Hypertrophic Cardiomyopathy 68 1.095
314
CRC021 Carcinosarcoma 62 1.094
315
CLN015 Colon Adenocarcinoma 64 1.087
316
HGH043 High Grade Glioma 46 1.081
317
P PRS038 Personality Disorder 65 1.077
318
CLR109 Colorectal Adenocarcinoma 50 1.075
319
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.073
320
ATS010 Autosomal Recessive Disease 42 1.057
321
P PLM036 Pulmonary Fibrosis 65 1.055
322
P CHR345 Chronic Pain 50 1.045
323
P CNJ013 Conjunctivitis 66 1.042
324
P THL005 Thalassemia 56 1.042
325
c CHR064 Chronic Monocytic Leukemia 35 1.041
326
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 1.039
327
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.037
328
GST040 Gastric Adenocarcinoma 66 1.034
329
c XRD022 Xeroderma Pigmentosum, Complementation Group D 56 1.021
330
CNG069 Congenital Cytomegalovirus 51 1.017
331
TRN015 Transient Cerebral Ischemia 62 1.015
332
c GLL024 Gallbladder Disease 1 53 1.007
333
SFT003 Soft Tissue Sarcoma 43 0.997
334
P SCK005 Sickle Cell Disease 56 0.992
335
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.988
336
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.984
337
P BNG032 Benign Mesothelioma 53 0.977
338
P GRF003 Graft-Versus-Host Disease 71 0.975
339
LYM027 Lymphopenia 56 0.968
340
URM002 Uremia 47 0.967
341
PST092 Posttransplant Acute Limbic Encephalitis 29 0.963
342
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.962
343
PST011 Pustulosis of Palm and Sole 52 0.962
344
P PSR002 Psoriasis 63 0.962
345
HDN002 Head Injury 44 0.960
346
WLK001 Walker-Warburg Syndrome 62 0.956
347
HMT002 Hematologic Cancer 61 0.955
348
DSS032 Disease by Infectious Agent 55 0.953
349
P TMP001 Temporal Lobe Epilepsy 49 0.951
350
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.950
351
P RSP003 Respiratory Failure 73 0.944
352
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.943
353
CRB009 Cerebritis 43 0.943
354
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.943
355
AND005 Androgen Insensitivity Syndrome, Mild 21 0.943
356
SPL004 Splenic Marginal Zone Lymphoma 50 0.940
357
MTH009 Mouth Disease 57 0.935
358
P ADL010 Adult Respiratory Distress Syndrome 70 0.934
359
TRY001 Trypanosomiasis 50 0.917
360
HPT022 Hepatoblastoma 54 0.917
361
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.917
362
P CTN015 Cutaneous T Cell Lymphoma 48 0.914
363
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.904
364
c BTT014 Beta-Thalassemia 72 0.904
365
SCH014 Schistosomiasis 56 0.904
366
c HYP595 Hypertension, Essential 84 0.901
367
DBT010 Diabetic Neuropathy 54 0.899
368
P SCL009 Sclerosing Cholangitis 46 0.890
369
P MYC008 Myocarditis 59 0.884
370
IGR001 Ige Responsiveness, Atopic 58 0.882
371
P RHN004 Rhinitis 56 0.881
372
YLL002 Yellow Fever 61 0.880
373
P NPH012 Nephrotic Syndrome 61 0.879
374
PLM031 Poliomyelitis 62 0.869
375
ADR005 Adrenal Carcinoma 58 0.869
376
P SLP005 Sleep Disorder 61 0.869
377
c CHL119 Cholangitis, Primary Sclerosing 57 0.867
378
STR067 Stroke, Ischemic 79 0.861
379
c SVR005 Severe Pre-Eclampsia 49 0.858
380
NRF007 Neurofibroma 63 0.858
381
CHR066 Chronic Fatigue Syndrome 59 0.857
382
DPH001 Diphtheria 59 0.857
383
CTN007 Cutaneous Leishmaniasis 61 0.851
384
c RNG021 Ring Chromosome 5 20 0.851
385
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.848
386
END057 Endometrial Cancer 76 0.847
388
P MLN069 Melanoma, Uveal 59 0.844
389
P RTN018 Retinal Disease 53 0.843
390
P HYP086 Hypothyroidism 68 0.837
391
ALB002 Albinism 46 0.837
392
CLR108 Colorectal Adenoma 63 0.830
393
DSS009 Disseminated Intravascular Coagulation 56 0.827
394
P HYP069 Hyperparathyroidism 62 0.827
395
P PRS040 Prostate Cancer 95 0.824
396
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.824
397
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.824
398
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.824
399
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.824
400
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.824
401
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.824
402
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.824
403
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.824
404
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.824
405
c MST023 Mesothelioma, Malignant 56 0.822
406
CLR030 Clear Cell Renal Cell Carcinoma 53 0.819
407
MCS002 Mucositis 55 0.813
408
CHL028 Childhood Type Dermatomyositis 58 0.812
409
P SYS005 Systemic Scleroderma 73 0.811
410
P SJG008 Sjogren Syndrome 60 0.806
411
c ACT135 Acute Graft Versus Host Disease 51 0.802
412
P DRM053 Dermatitis, Atopic 65 0.801
413
BRT005 Barth Syndrome 55 0.801
414
MLD002 Mild Pre-Eclampsia 33 0.801
415
P INS002 in Situ Carcinoma 52 0.801
416
RBS001 Rabies 57 0.799
417
PSR001 Psoriatic Arthritis 61 0.798
418
P OCL002 Oculocutaneous Albinism 59 0.798
419
c ACT068 Acute Cystitis 60 0.798
420
BRR014 Barrett Esophagus 66 0.795
421
MCR004 Macroglobulinemia 48 0.784
422
SCK003 Sickle Cell Anemia 74 0.782
423
c NRF024 Neurofibromatosis, Type I 76 0.777
424
BRN056 Bronchopulmonary Dysplasia 57 0.777
425
P TST021 Testicular Germ Cell Tumor 61 0.773
426
P ECT006 Ectodermal Dysplasia 62 0.773
427
c SVR003 Severe Congenital Neutropenia 59 0.773
428
PPT005 Peptic Ulcer Disease 58 0.773
429
GRM010 Germ Cells Tumors 33 0.773
430
OBN001 Ouabain Resistance 15 0.770
431
PRP030 Purpura 54 0.770
432
P GLL022 Guillain-Barre Syndrome 59 0.770
433
INT075 Intracranial Hypertension 52 0.769
434
P ALC033 Alcohol Use Disorder 67 0.768
435
OTT002 Otitis Media 70 0.767
436
OVR059 Ovary Adenocarcinoma 49 0.767
437
LYM021 Lymphadenitis 55 0.756
438
IGG001 Iga Glomerulonephritis 50 0.748
439
EHR002 Ehrlichiosis 39 0.746
440
NWC001 Newcastle Disease 47 0.746
441
WLL004 Wallerian Degeneration 38 0.742
442
P OVR082 Overgrowth Syndrome 41 0.742
443
MYL005 Myelofibrosis 70 0.742
444
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.741
445
P MCR129 Microvascular Complications of Diabetes 1 67 0.734
446
c MCR112 Microvascular Complications of Diabetes 2 42 0.734
447
SLC006 Silicosis 55 0.734
448
PNM008 Pneumothorax 54 0.734
449
CCN002 Cocaine Abuse 49 0.734
450
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.734
451
ACR008 Acrocallosal Syndrome 69 0.731
452
P OLG002 Oligodendroglioma 66 0.727
453
WST002 Western Equine Encephalitis 39 0.713
454
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.710
455
c JVN010 Juvenile Rheumatoid Arthritis 52 0.710
456
SRF006 Surfactant Dysfunction 33 0.710
457
P LYM033 Lymphoproliferative Syndrome 59 0.706
458
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.702
459
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.699
460
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.699
461
PLC005 Placental Insufficiency 55 0.699
462
TNG007 Tongue Carcinoma 55 0.699
463
P THY032 Thyroiditis 56 0.699
464
MYL031 Myeloproliferative Neoplasm 66 0.696
465
FND002 Fundus Dystrophy 54 0.692
466
PRT058 Pure Autonomic Failure 58 0.692
467
c INH030 Inherited Retinal Disorder 28 0.692
468
HYP264 Hypertonia 35 0.692
469
P PRN023 Prion Disease 60 0.689
470
CNG034 Congestive Heart Failure 69 0.676
471
LGN006 Legionnaire Disease 52 0.671
472
END041 Endometrial Adenocarcinoma 63 0.671
473
c BPL002 Bipolar I Disorder 47 0.657
474
P NRV007 Nervous System Disease 65 0.657
475
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.657
476
PRL017 Prolymphocytic Leukemia 47 0.657
477
P ESN008 Eosinophilic Pneumonia 50 0.647
478
GRW007 Growth Hormone Deficiency 47 0.647
479
LYM012 Lymphoplasmacytic Lymphoma 50 0.642
480
P CRN024 Corneal Disease 43 0.632
481
CYT005 Cytomegalovirus Retinitis 50 0.632
482
PLS007 Plasmodium Falciparum Malaria 52 0.632
483
MLG079 Malignant Pleural Mesothelioma 42 0.632
484
SPS057 Spasticity 43 0.629
485
c ANM038 Anemia, Autoimmune Hemolytic 63 0.614
486
DGR001 Digeorge Syndrome 62 0.614
487
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.614
488
P CNG001 Congenital Myasthenic Syndrome 68 0.614
489
BBS001 Babesiosis 48 0.614
490
CHL045 Choline Deficiency Disease 39 0.611
491
NTR005 Nutritional Deficiency Disease 60 0.600
492
WLD007 Waldenstroem's Macroglobulinemia 59 0.600
493
ANG046 Angioimmunoblastic T-Cell Lymphoma 50 0.600
494
SZR001 Sezary's Disease 60 0.600
495
P TYR004 Tyrosinemia 49 0.597
496
CRB090 Cerebral Hypoxia 42 0.574
497
c OVR114 Ovarian Cancer 1 60 0.564
498
PRP016 Paraplegia 52 0.547
499
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.523
500
AGG012 Aggressive Nk-Cell Leukemia 47 0.522
501
c VRL005 Viral Pneumonia 52 0.522
502
P CNT005 Central Nervous System Lymphoma 51 0.522
503
PNM001 Pneumocystosis 60 0.522
504
PRM226 Primary Central Nervous System Lymphoma 47 0.522
505
KRT006 Keratoconjunctivitis 53 0.522
506
P TMR010 Tumor Predisposition Syndrome 69 0.521
507
PPL022 Papilloma 53 0.515
508
P SZR006 Seizure Disorder 69 0.513
509
P DRR001 Diarrhea 55 0.508
510
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.502
511
INH023 Inherited Cancer-Predisposing Syndrome 53 0.502
512
PTT037 Pituitary Tumors 44 0.496
513
SQM002 Squamous Cell Papilloma 45 0.495
514
URD002 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to 26 0.493
515
HMC014 Homocysteinemia 52 0.491
516
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.491
517
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.473
518
P ATR005 Atrophic Gastritis 50 0.469
519
PRM236 Primary Biliary Cholangitis 62 0.466
520
NRM005 Neuromuscular Disease 62 0.464
521
HRW001 Hair Whorl 35 0.461
522
ACT003 Acute Kidney Tubular Necrosis 46 0.461
523
P CTR002 Cataract 59 0.440
524
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.422
525
DRM006 Dermatitis 61 0.413
526
P RNL017 Renal Oncocytoma 54 0.410
527
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.402
528
P KDN017 Kidney Cancer 60 0.401
529
ALL003 Allergic Rhinitis 66 0.401
530
P FRG001 Fragile X Syndrome 70 0.396
531
MLD018 Mild Cognitive Impairment 48 0.394
532
c ATS007 Autism Spectrum Disorder 71 0.392
533
P HYP750 Hypertriglyceridemia, Familial 61 0.392
534
c THY107 Thymoma, Familial 42 0.389
535
P THY023 Thymoma 64 0.389
536
P PLY019 Polyneuropathy 52 0.389
537
PRM329 Premature Aging 36 0.389
538
P SDR003 Sideroblastic Anemia 49 0.377
539
MNN009 Meningoencephalitis 47 0.371
540
WST005 West Nile Virus 55 0.367
541
ENT004 Enthesopathy 51 0.364
542
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.362
543
P LYN001 Lynch Syndrome 76 0.362
544
P ATS364 Autism 72 0.359
545
HMS001 Hemosiderosis 48 0.359
546
DMY004 Demyelinating Disease 50 0.359
547
P RRH023 Rare Hereditary Hemochromatosis 52 0.359
548
P AGM001 Agammaglobulinemia 67 0.359
549
P MYT002 Myotonic Dystrophy 51 0.350
550
GLS001 Gliosarcoma 63 0.347
551
P DMN002 Dementia 65 0.347
552
P RBL001 Rubella 58 0.337
553
KRT009 Keratosis 52 0.334
554
BRN018 Borna Disease 36 0.334
555
GNT003 Genital Herpes 54 0.334
556
EMB004 Embryonal Carcinoma 55 0.332
557
c HPT007 Hepatitis E 50 0.332
558
c HRD010 Hereditary Spastic Paraplegia 65 0.321
559
HMP005 Hemiplegia 53 0.321
560
CHR178 Chromosomal Triplication 33 0.321
561
HND015 Hand Skill, Relative 29 0.313
562
HMG005 Hemoglobinopathy 55 0.313
563
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.307
564
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.307
565
CRB037 Cerebral Palsy 66 0.307
566
CRL001 Cerulean Cataract 26 0.305
567
P CND004 Candidiasis 57 0.299
568
GLM044 Glomerular Disease 34 0.299
569
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.292
570
P GLY013 Glycogen Storage Disease 59 0.292
571
P GLL018 Gallbladder Cancer 59 0.292
572
P END033 Endocarditis 58 0.292
573
P PRG013 Paraganglioma 57 0.286
574
c FNC027 Fanconi Anemia, Complementation Group a 80 0.286
575
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 39 0.286
576
P MMP001 Mumps 56 0.281
577
TNS005 Tonsillitis 57 0.281
578
c CNG027 Congenital Hemolytic Anemia 49 0.281
579
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.281
580
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.281
581
P SML001 Small Cell Carcinoma 52 0.278
582
CLF027 Cleft Palate, Isolated 64 0.278
583
HND002 Hand, Foot and Mouth Disease 50 0.278
584
TRT001 Teratocarcinoma 41 0.278
585
LST001 Listeriosis 59 0.278
586
P MTH007 Methemoglobinemia 46 0.278
587
VNZ002 Venezuelan Equine Encephalitis 45 0.278
588
CND006 Candida Glabrata 29 0.278
589
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.278
590
P FML011 Familial Adenomatous Polyposis 70 0.275
591
CHR103 Charge Syndrome 65 0.275
592
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.275
593
P PTT006 Pituitary Adenoma 55 0.275
594
c SCN007 Secondary Hyperparathyroidism 50 0.275
595
JPN002 Japanese Encephalitis 61 0.275
596
P CRD246 Cardiovascular System Disease 55 0.275
597
CRY005 Cryptococcosis 61 0.275
598
c INH020 Inherited Metabolic Disorder 47 0.275
599
P MDL005 Medulloblastoma 75 0.257
600
AGM019 Agammaglobulinemia, X-Linked 71 0.257
601
ENT011 Enterocolitis 55 0.257
602
P WSK001 Wiskott-Aldrich Syndrome 72 0.257
603
PSY004 Psychotic Disorder 66 0.257
604
c HPT003 Hepatitis a 63 0.257
605
MCR011 Microinvasive Gastric Cancer 41 0.257
606
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.257
607
PLC008 Placenta Disease 48 0.257
608
CRV002 Cervix Uteri Carcinoma in Situ 48 0.257
609
PRN019 Perinatal Necrotizing Enterocolitis 60 0.257
610
CRV045 Cervical Intraepithelial Neoplasia 38 0.257
611
P AVS003 Avascular Necrosis 41 0.257
612
SBC001 Subacute Sclerosing Panencephalitis 53 0.254
613
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.254
614
ABT001 Abetalipoproteinemia 68 0.254
615
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.254
616
HMN001 Human Monocytic Ehrlichiosis 29 0.254
617
BTT017 Beta-Thalassemia Major 54 0.254
618
TRD006 Tardive Dyskinesia 53 0.254
619
HSH003 Hashimoto Thyroiditis 60 0.254
620
c SPN294 Spinocerebellar Ataxia 1 53 0.254
621
P MST009 Mastocytosis 64 0.254
622
P LCH002 Lichen Planus 54 0.254
623
WTH001 Withdrawal Disorder 47 0.236
624
CLB010 Coloboma of Macula 53 0.236
625
RTC009 Reticulum Cell Sarcoma 43 0.236
626
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.236
627
P MMB011 Membranous Nephropathy 50 0.236
628
TCL003 T Cell Deficiency 44 0.236
629
TRN018 Transitional Cell Carcinoma 56 0.236
630
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.236
631
P CCK001 Cockayne Syndrome 67 0.236
632
AMN003 Amnestic Disorder 53 0.236
633
URL001 Urolithiasis 45 0.236
634
ANP009 Anaplastic Oligodendroglioma 41 0.236
635
c BCT007 Bacterial Meningitis 55 0.236
636
c BCT013 Bacterial Pneumonia 47 0.236
637
P ACT008 Actinic Keratosis 53 0.236
638
MLL001 Molluscum Contagiosum 48 0.236
639
LKP003 Leukoplakia 39 0.236
640
IMM076 Immunodeficiency 24 31 0.222
641
THY006 Thymus Lymphoma 27 0.222
642
P AML002 Amelogenesis Imperfecta 56 0.222
643
DWR001 Dwarfism 44 0.222
644
GLY010 Glycine Encephalopathy 57 0.212
645
PFF001 Pfeiffer Syndrome 77 0.212
646
c WLM013 Wilms Tumor 1 65 0.212
647
P LSS002 Lissencephaly 52 0.212
649
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.212
650
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 0.212
651
P FTL001 Fetal Alcohol Syndrome 55 0.212
652
HPT046 Hepatic Veno-Occlusive Disease 54 0.212
653
PPL002 Papillary Carcinoma 46 0.212
654
P INT068 Intestinal Disease 53 0.212
655
FCL012 Facial Paralysis 49 0.212
656
AMN001 Amenorrhea 53 0.212
657
CMM005 Common Cold 55 0.212
658
NRM001 Neuromyelitis Optica 60 0.212
659
DHY008 Dihydroxyadeninuria 24 0.212
660
STT041 Stuttering 52 0.179
661
INT029 Interleukin-7 Receptor Alpha Deficiency 27 0.179
662
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.179
663
LYN004 Lynch Syndrome I 60 0.179
664
SMT008 Smith-Magenis Syndrome 53 0.179
665
c MCP050 Mucopolysaccharidosis, Type Ii 73 0.179
666
SPP011 Suppression of Tumorigenicity 12 61 0.179
667
OMN001 Omenn Syndrome 63 0.179
668
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.179
669
c ALZ014 Alzheimer Disease 16 24 0.179
670
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.179
671
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.179
672
PLT004 Platelet Glycoprotein Iv Deficiency 55 0.179
673
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.179
674
NND010 Nondisjunction 34 0.179
675
SPN028 Spondyloepimetaphyseal Dysplasia, Strudwick Type 50 0.179
676
FCT007 Factor Vii Deficiency 64 0.179
677
QFV001 Q Fever 61 0.179
678
c CHR418 Chronic Leukemia 48 0.179
679
P RCT021 Rectum Cancer 54 0.179
680
P THR015 Thrombophilia 51 0.179
681
BCL002 B Cell Deficiency 40 0.179
682
VGN023 Vaginitis 56 0.179
683
PLM012 Pulmonary Sarcoidosis 52 0.179
684
SYS004 Systemic Mastocytosis 62 0.179
685
P MLT074 Multiple Endocrine Neoplasia 58 0.179
686
PRG009 Progressive Multifocal Leukoencephalopathy 58 0.179
687
ISC001 Ischemic Neuropathy 27 0.179
688
MNC001 Monocular Esotropia 30 0.179
689
P LNG035 Lung Large Cell Carcinoma 53 0.179
690
CNG017 Congenital Nonspherocytic Hemolytic Anemia 34 0.179
691
BLL003 Bell's Palsy 48 0.179
692
P TRT010 Teratoma 50 0.179
693
CHL040 Cholangiolocellular Carcinoma 33 0.179
694
BWN006 Bowen's Disease 32 0.179
695
PLM035 Pulmonary Eosinophilia 49 0.179
696
DFF036 Differentiated Thyroid Carcinoma 51 0.179
697
ORL013 Oral Lichen Planus 45 0.179
698
EST005 Esotropia 43 0.179
700
c 46X071 46,xy Disorder of Sexual Development Due to Dihydrotestosterone Backdoor Pathway Biosynthesis Defect 42 0.179
701
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 0.179
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