Search results for Cytidine monophosphate

642 hits were found for Cytidine monophosphate

# Family MCID Name MIFTS Score
1
URD002 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to 26 33.992
2
CHL014 Cholera 62 8.534
3
P LKM002 Leukemia 66 7.022
4
P NRB001 Neuroblastoma 66 6.790
5
P LKM071 Leukemia, Chronic Lymphocytic 74 6.146
6
PRT037 Pertussis 49 6.078
7
c LKM061 Leukemia, Acute Myeloid 83 5.971
8
HMN044 Human Immunodeficiency Virus Type 1 76 5.721
9
P LYM118 Lymphoma 69 5.638
10
MYL009 Myelodysplastic Syndrome 67 5.363
11
P MYL006 Myeloid Leukemia 60 5.158
12
c MJR024 Major Affective Disorder 9 40 5.154
13
c MJR022 Major Affective Disorder 8 37 5.154
14
P BPL003 Bipolar Disorder 56 5.154
15
P BCL017 B-Cell Lymphoma 57 5.124
16
P LKM062 Leukemia, Acute Lymphoblastic 69 4.845
17
IMM167 Immune Deficiency Disease 77 4.690
18
P PNC035 Pancreatic Cancer 86 4.564
19
c ACT073 Acute Leukemia 59 4.476
20
HLX001 Helix Syndrome 47 4.449
21
c HPT016 Hepatitis B 62 4.438
22
P HRP006 Herpes Simplex 65 4.393
23
P HML002 Hemolytic Anemia 62 4.179
24
MNT002 Mental Depression 56 4.137
25
DPR016 Depression 65 4.091
26
END040 Endogenous Depression 54 3.914
27
MYL069 Myeloma, Multiple 77 3.814
28
c HPT073 Hepatitis C Virus 71 3.781
29
P AST005 Asthma 76 3.733
30
HYP266 Hypoxia 56 3.601
31
RPD005 Rapidly Involuting Congenital Hemangioma 48 3.560
32
P HYP069 Hyperparathyroidism 62 3.554
33
c HPT001 Hepatitis C 61 3.507
34
48X005 48,xyyy 39 3.502
35
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.455
36
NRR001 Neuroretinitis 42 3.439
37
RTN023 Retinitis 45 3.439
38
DFC004 Deficiency Anemia 74 3.420
39
P RHN004 Rhinitis 57 3.419
40
P HPT023 Hepatocellular Carcinoma 95 3.412
41
GLL048 Glial Tumor 52 3.377
42
P HPT021 Hepatitis 68 3.348
43
ALL003 Allergic Rhinitis 66 3.339
44
ALL006 Allergic Asthma 56 3.338
45
GLM045 Glioma 62 3.324
46
ADR040 Adrenal Gland Pheochromocytoma 45 3.299
47
P PHC003 Pheochromocytoma 70 3.299
48
c PRC016 Pre-Eclampsia 64 3.253
49
HYP066 Hyperglycemia 60 3.249
50
P PLM037 Pulmonary Hypertension 69 3.136
51
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.117
52
P ADN016 Adenocarcinoma 63 3.065
53
ISC004 Ischemia 61 3.059
54
PNC129 Pancreatic Adenocarcinoma 65 3.037
55
OST159 Osteogenic Sarcoma 66 3.035
56
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.007
57
P GRV001 Graves' Disease 54 2.968
58
NRT001 Neurotic Disorder 56 2.943
59
P MJR007 Major Affective Disorder 1 42 2.939
60
P HYP076 Hyperthyroidism 53 2.934
61
P GST053 Gastric Cancer 82 2.872
62
BRK010 Burkitt Lymphoma 66 2.838
63
P FLL037 Follicular Lymphoma 73 2.830
64
FTT001 Fatty Liver Disease 61 2.829
65
BNR002 Bone Resorption Disease 47 2.826
66
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.824
67
P GRF003 Graft-Versus-Host Disease 71 2.803
68
P LVR013 Liver Disease 68 2.780
69
c SYS001 Systemic Lupus Erythematosus 86 2.778
70
VCC001 Vaccinia 49 2.775
71
ALL029 Allergic Disease 61 2.768
72
P LNG032 Lung Cancer 98 2.759
73
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.728
74
DFF005 Diffuse Large B-Cell Lymphoma 55 2.718
75
P RTN008 Retinitis Pigmentosa 79 2.711
76
CYS001 Cystic Fibrosis 77 2.693
77
P INF038 Influenza 68 2.668
78
P CLR023 Colorectal Cancer 100 2.605
79
ACT098 Acute Erythroid Leukemia 55 2.605
80
IGR001 Ige Responsiveness, Atopic 59 2.604
81
P NTR004 Neutropenia 62 2.603
82
c SML038 Small Cell Cancer of the Lung 69 2.601
83
LYM143 Lymphoma, Non-Hodgkin, Familial 79 2.582
84
LYM019 Lymphosarcoma 46 2.580
85
P NRP001 Neuropathy 59 2.553
86
P LPS004 Lupus Erythematosus 61 2.548
87
ADN018 Adenoma 58 2.527
88
ANX004 Anoxia 40 2.522
89
BRN071 Brain Injury 50 2.497
90
OCL069 Ocular Motor Apraxia 57 2.491
91
LYM133 Lymphoma, Hodgkin, Classic 74 2.485
92
GLB002 Glioblastoma 67 2.454
93
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.441
94
PTT037 Pituitary Tumors 44 2.407
95
CLT003 Colitis 63 2.403
96
P DRM053 Dermatitis, Atopic 65 2.403
97
P MLN008 Melanoma 75 2.401
98
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.399
99
c LKM005 Leukemia, T-Cell, Chronic 33 2.399
100
P MYP004 Myopathy 67 2.382
101
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.375
102
P GST044 Gastritis 55 2.357
103
c LKM063 Leukemia, Chronic Myeloid 71 2.347
104
P ECL001 Eclampsia 52 2.330
105
P FBR017 Fibrosarcoma 55 2.298
106
P TRM003 Tremor 50 2.289
107
c MCR113 Microvascular Complications of Diabetes 3 52 2.280
108
PPT005 Peptic Ulcer Disease 58 2.276
109
c MCR133 Microvascular Complications of Diabetes 4 41 2.275
110
c MCR130 Microvascular Complications of Diabetes 6 41 2.275
111
c MCR120 Microvascular Complications of Diabetes 7 47 2.275
112
P ANR048 Aniridia 1 66 2.271
113
P GLM040 Glioma Susceptibility 1 70 2.264
114
c PCH010 Pachyonychia Congenita 3 43 2.263
115
MLG169 Malignant Astrocytoma 57 2.258
116
P SCK005 Sickle Cell Disease 56 2.258
117
P OPN001 Open-Angle Glaucoma 55 2.249
118
c HYP595 Hypertension, Essential 84 2.228
119
P TRN020 Turner Syndrome 67 2.224
120
P MYC084 Mycobacterium Tuberculosis 1 68 2.221
121
P OVR042 Ovarian Cancer 88 2.178
122
AGN016 Aging 54 2.173
123
P MSC005 Muscular Dystrophy 66 2.160
124
c PLM164 Pulmonary Hypertension, Primary, 1 80 2.143
125
c CHR064 Chronic Monocytic Leukemia 36 2.141
126
PRT251 Proteinuria, Chronic Benign 58 2.127
127
ATM095 Autoimmune Disease 61 2.121
128
ACT119 Acute Promyelocytic Leukemia 62 2.095
129
P VSC007 Vascular Disease 62 2.085
130
DWN001 Down Syndrome 70 2.071
131
BRN004 Brain Edema 54 2.070
132
P INF037 Inflammatory Bowel Disease 53 2.069
133
GST045 Gastroenteritis 58 2.069
134
P CRD119 Cardiac Arrest 68 2.061
135
P BRS047 Breast Cancer 97 2.055
136
THY029 Thyroid Carcinoma 54 2.052
137
CHC001 Chickenpox 56 2.045
138
MDD011 Mood Disorder 62 2.033
139
HYP056 Hypoglycemia 65 2.023
140
BCT022 Bacterial Infectious Disease 56 2.012
141
LVR012 Liver Cirrhosis 62 2.007
142
CRB039 Cerebrovascular Disease 65 1.992
143
ORL015 Oral Squamous Cell Carcinoma 43 1.990
144
KRT019 Keratitis, Hereditary 66 1.990
145
P GLM007 Glomerulonephritis 59 1.980
146
P HYP086 Hypothyroidism 69 1.972
147
RCK004 Rickets 65 1.957
148
SKN016 Skin Disease 62 1.954
149
HMP009 Haemophilus Influenzae 41 1.952
150
P HYP098 Hypereosinophilic Syndrome 66 1.938
151
P NPH012 Nephrotic Syndrome 62 1.934
152
P RHM011 Rheumatoid Arthritis 81 1.933
153
c MCR115 Microvascular Complications of Diabetes 5 65 1.931
154
ARG004 Argyria 26 1.923
155
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.922
156
P THR014 Thrombocytopenia 66 1.920
157
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.909
158
P VSC011 Vasculitis 61 1.886
159
P LNG064 Lung Cancer Susceptibility 3 70 1.881
160
GRN017 Granulocytopenia 42 1.878
161
DRM006 Dermatitis 62 1.870
162
AND005 Androgen Insensitivity Syndrome, Mild 21 1.870
163
P MJR001 Major Depressive Disorder 68 1.864
164
MSL001 Measles 61 1.861
165
TXC005 Toxic Shock Syndrome 62 1.859
166
STM007 Stomatitis 52 1.850
167
c VRL010 Viral Hepatitis 52 1.846
168
P OPT006 Optic Nerve Disease 57 1.843
169
c ATM011 Autoimmune Hepatitis 62 1.832
170
47X002 47,xyy 48 1.831
171
P ENC004 Encephalitis 61 1.831
172
TRM010 Traumatic Brain Injury 50 1.831
173
P BLD134 Bladder Cancer 79 1.828
174
CRV035 Cervical Cancer 72 1.827
175
ESP021 Esophageal Cancer 84 1.810
176
P RTN024 Retinoblastoma 72 1.808
177
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.805
178
c HYP836 Hypercholesterolemia, Familial, 1 73 1.798
179
CRB004 Cerebral Artery Occlusion 46 1.793
180
c GLC092 Glaucoma, Primary Open Angle 61 1.786
181
SPL018 Splenomegaly 47 1.772
182
OVR094 Ovarian Epithelial Cancer 39 1.755
183
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.731
184
HRY003 Hairy Cell Leukemia 61 1.728
185
SPN186 Spinal Cord Injury 61 1.727
186
CNG034 Congestive Heart Failure 69 1.726
187
c TYP009 Type 2 Diabetes Mellitus 92 1.713
188
P MLN007 Male Infertility 56 1.705
189
MYL031 Myeloproliferative Neoplasm 66 1.700
190
P INF032 Infertility 60 1.697
191
PPL052 Papillomatosis, Confluent and Reticulated 34 1.689
192
LPD008 Lipid Metabolism Disorder 61 1.686
193
SLP001 Sleeping Sickness 56 1.680
194
MLR004 Malaria 78 1.678
195
DBT010 Diabetic Neuropathy 54 1.678
196
HLC007 Helicobacter Pylori Infection 67 1.650
197
ULC004 Ulcerative Colitis 74 1.630
198
P ADL010 Adult Respiratory Distress Syndrome 71 1.626
199
HPT004 Hepatic Coma 43 1.622
200
P DBT009 Diabetes Mellitus 67 1.622
201
SQM006 Squamous Cell Carcinoma 59 1.621
202
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.616
203
P PRD008 Periodontitis 64 1.611
204
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.608
205
P ENC018 Encephalopathy 62 1.608
206
P PSR002 Psoriasis 63 1.606
207
PRS045 Prostatic Hypertrophy 52 1.605
208
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.604
209
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.604
210
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.604
211
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.604
212
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.604
213
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.604
214
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.604
215
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.604
216
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.604
217
BRN056 Bronchopulmonary Dysplasia 57 1.603
218
P PRP019 Peripheral Nervous System Disease 57 1.596
219
PST011 Pustulosis of Palm and Sole 52 1.588
220
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.582
221
PLS011 Plasmacytoma 56 1.580
222
P SZR006 Seizure Disorder 69 1.568
223
CHG001 Chagas Disease 65 1.559
224
GST040 Gastric Adenocarcinoma 66 1.555
225
CLN015 Colon Adenocarcinoma 64 1.555
226
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.552
227
P LTR001 Lateral Sclerosis 58 1.552
228
TLN003 Telangiectasis 51 1.531
229
ALL014 Allergic Encephalomyelitis 34 1.530
230
P SPP010 Suppressor of Tumorigenicity 3 51 1.527
231
CYT002 Cytokine Deficiency 43 1.521
232
DSS032 Disease by Infectious Agent 55 1.518
233
PLG002 Plague 58 1.510
234
P ATX030 Ataxia-Telangiectasia 80 1.502
235
PRS129 Prostatic Hyperplasia, Benign 48 1.502
236
TRT001 Teratocarcinoma 41 1.492
237
P CHR285 Chronic Myelomonocytic Leukemia 59 1.491
238
c HPT015 Hepatitis D 49 1.482
239
XRD010 Xeroderma Pigmentosum, Variant Type 72 1.475
240
LNG099 Lung Disease 62 1.474
241
P CNR004 Cone-Rod Dystrophy 2 75 1.469
242
c DLT002 Dilated Cardiomyopathy 79 1.469
243
PRS021 Prostatic Adenoma 43 1.465
244
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.465
245
HYP005 Hypokalemia 55 1.458
246
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.447
247
SCH014 Schistosomiasis 56 1.447
248
c ACT027 Acute Pancreatitis 60 1.446
249
c SCN007 Secondary Hyperparathyroidism 51 1.445
250
CHL065 Cholangiocarcinoma 58 1.443
251
INT079 Intrahepatic Cholangiocarcinoma 51 1.443
252
P INS002 in Situ Carcinoma 53 1.442
253
c HMN021 Human T-Cell Leukemia Virus Type 1 46 1.437
254
P UVT001 Uveitis 57 1.429
255
P PRS040 Prostate Cancer 95 1.427
256
P SKN015 Skin Carcinoma 71 1.420
257
END086 End Stage Renal Disease 54 1.416
258
P ALC033 Alcohol Use Disorder 67 1.408
259
P SBS003 Substance Abuse 54 1.407
260
ATH013 Atherosclerosis Susceptibility 63 1.407
261
P PNC044 Pancreatitis 61 1.396
262
HND015 Hand Skill, Relative 29 1.386
263
TTN003 Tetanus 64 1.383
264
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.377
265
GT001 Gout 63 1.376
266
NRF007 Neurofibroma 64 1.364
267
P EXN002 Exanthem 58 1.360
268
OST012 Osteoarthritis 77 1.359
269
DPH001 Diphtheria 59 1.354
270
NNL006 Non-Alcoholic Steatohepatitis 54 1.335
271
STR067 Stroke, Ischemic 79 1.332
272
c SVR005 Severe Pre-Eclampsia 50 1.331
273
CRT015 Carotid Artery Occlusion 45 1.331
274
P NRF002 Neurofibromatosis 60 1.329
275
AMB002 Amblyopia 49 1.319
276
SPP007 Suppression Amblyopia 38 1.319
277
PLY150 Polykaryocytosis Inducer 29 1.313
278
SVR004 Severe Combined Immunodeficiency 71 1.311
279
ORL011 Oral Cancer 60 1.309
280
TRN015 Transient Cerebral Ischemia 62 1.301
281
CMM004 Common Variable Immunodeficiency 72 1.293
282
MSC007 Muscle Hypertrophy 64 1.291
283
P TMP001 Temporal Lobe Epilepsy 49 1.291
284
P MNC007 Monocytic Leukemia 48 1.291
285
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.285
286
P SYS005 Systemic Scleroderma 73 1.277
287
SCK003 Sickle Cell Anemia 74 1.264
288
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.264
289
WTH001 Withdrawal Disorder 47 1.258
290
VSC002 Vascular Dementia 59 1.254
291
SRC014 Sarcoma 64 1.242
292
SPN035 Spindle Cell Sarcoma 51 1.242
293
CHL068 Cholestasis 61 1.239
294
HMN047 Human Cytomegalovirus Infection 59 1.239
295
MNT001 Mantle Cell Lymphoma 65 1.239
296
P ALZ034 Alzheimer Disease 87 1.234
297
MYL005 Myelofibrosis 70 1.225
298
P RTN018 Retinal Disease 53 1.220
299
URM002 Uremia 47 1.219
300
ACQ007 Acquired Immunodeficiency Syndrome 58 1.217
301
LYM040 Lymphoblastic Lymphoma 53 1.216
302
TRY001 Trypanosomiasis 50 1.216
303
P HRT032 Heart Disease 84 1.213
304
P ADL017 Adult T-Cell Leukemia 54 1.205
305
c ATR087 Atrial Standstill 1 74 1.200
306
P DRR001 Diarrhea 55 1.194
307
c CHR684 Chronic Kidney Disease 74 1.192
308
P KDN018 Kidney Disease 72 1.190
309
P BRS044 Breast Adenocarcinoma 58 1.190
310
KRT002 Keratomalacia 54 1.167
311
P THY032 Thyroiditis 56 1.164
312
ALP103 Alpha-1-Antitrypsin Deficiency 67 1.162
313
LYM027 Lymphopenia 56 1.157
314
CRC021 Carcinosarcoma 62 1.154
315
P PLM036 Pulmonary Fibrosis 65 1.144
316
DWR001 Dwarfism 45 1.139
317
P ART022 Arthritis 70 1.135
318
CHN002 Chancroid 36 1.128
319
SLD003 Sialadenitis 47 1.125
320
END057 Endometrial Cancer 71 1.121
321
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.112
322
ATS010 Autosomal Recessive Disease 42 1.110
323
c ACT135 Acute Graft Versus Host Disease 51 1.109
324
P GLY013 Glycogen Storage Disease 59 1.103
325
NRM005 Neuromuscular Disease 63 1.097
326
c CNG027 Congenital Hemolytic Anemia 49 1.092
327
P PRK039 Parkinsonism 55 1.075
328
PRT036 Peritonitis 65 1.072
329
CMB007 Combined Immunodeficiency 56 1.072
330
c BCT007 Bacterial Meningitis 55 1.070
331
HGH043 High Grade Glioma 46 1.055
332
P PTT006 Pituitary Adenoma 55 1.055
333
CHL123 Chlamydia 58 1.053
334
NWC001 Newcastle Disease 48 1.049
335
NCL008 Nuclear Ribonucleic Acid 15 1.047
336
PSR001 Psoriatic Arthritis 61 1.046
337
P MYC008 Myocarditis 59 1.040
338
KPS004 Kaposi Sarcoma 76 1.039
339
ALC007 Alcohol Dependence 65 1.016
340
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.015
341
HPT022 Hepatoblastoma 54 1.014
342
MSC157 Muscular Dystrophy, Duchenne Type 79 1.011
343
c INH020 Inherited Metabolic Disorder 47 1.010
344
AMN003 Amnestic Disorder 54 1.009
345
CLR108 Colorectal Adenoma 63 1.006
346
P PLY019 Polyneuropathy 53 1.004
347
P HYP061 Hypertrophic Cardiomyopathy 69 0.989
348
URL001 Urolithiasis 45 0.986
349
PPL002 Papillary Carcinoma 46 0.980
350
P THL005 Thalassemia 56 0.979
352
P CRN300 Coronary Heart Disease 1 73 0.974
353
P DNG005 Dengue Virus 55 0.969
354
P CHR345 Chronic Pain 50 0.969
355
c BRN108 Branchiootic Syndrome 1 63 0.963
356
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.960
357
c TYP008 Type 1 Diabetes Mellitus 77 0.950
358
PST092 Posttransplant Acute Limbic Encephalitis 29 0.947
359
P NSP012 Nasopharyngeal Carcinoma 60 0.940
360
MDD018 Middle East Respiratory Syndrome 44 0.940
361
P INT068 Intestinal Disease 53 0.934
362
HRW001 Hair Whorl 35 0.934
363
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.923
364
P CTR002 Cataract 59 0.919
365
c ACT071 Acute Kidney Failure 60 0.918
366
MLD018 Mild Cognitive Impairment 48 0.912
367
P OVR082 Overgrowth Syndrome 42 0.901
368
P RSP003 Respiratory Failure 74 0.896
369
SKN019 Skin Melanoma 70 0.890
370
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.885
371
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.864
372
BLR013 Biliary Tract Cancer 43 0.864
373
P CTN015 Cutaneous T Cell Lymphoma 48 0.860
374
P SRC025 Sarcoidosis 1 70 0.856
375
P HYP750 Hypertriglyceridemia, Familial 62 0.854
376
P THY023 Thymoma 64 0.852
377
c THY107 Thymoma, Familial 42 0.852
379
SYN007 Synovitis 54 0.846
380
PLC002 Plica Syndrome 35 0.846
381
P GLL022 Guillain-Barre Syndrome 59 0.845
382
HMC014 Homocysteinemia 52 0.840
383
P PRK057 Parkinson Disease, Late-Onset 79 0.840
384
BRT005 Barth Syndrome 55 0.838
385
P PNM007 Pneumonia 64 0.838
386
PLM031 Poliomyelitis 62 0.837
387
VTM002 Vitamin B12 Deficiency 48 0.832
388
P SCH015 Schizophrenia 74 0.829
389
CLF027 Cleft Palate, Isolated 64 0.827
390
HYP020 Hyperprolactinemia 63 0.810
391
c ACT134 Acute Liver Failure 57 0.810
392
GRM010 Germ Cells Tumors 33 0.804
393
PHN003 Phenylketonuria 76 0.804
394
WST005 West Nile Virus 55 0.802
395
P FRG001 Fragile X Syndrome 70 0.802
396
MTH009 Mouth Disease 57 0.800
397
CRH001 Crohn's Disease 80 0.794
398
MCR004 Macroglobulinemia 48 0.785
399
P CNJ013 Conjunctivitis 66 0.784
400
CLR030 Clear Cell Renal Cell Carcinoma 54 0.779
401
P TST021 Testicular Germ Cell Tumor 61 0.777
402
P SJG008 Sjogren Syndrome 61 0.777
403
ADN009 Adenosquamous Carcinoma 49 0.777
404
BNS003 Binswanger's Disease 41 0.777
405
CLR109 Colorectal Adenocarcinoma 50 0.772
406
P LCH002 Lichen Planus 55 0.769
407
GNT003 Genital Herpes 54 0.769
408
P MLN069 Melanoma, Uveal 59 0.767
409
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.767
410
OVR059 Ovary Adenocarcinoma 49 0.765
411
P ART023 Arthropathy 60 0.762
412
BCK006 Back Pain 43 0.762
413
P CHL066 Cholangitis 51 0.762
414
DMY004 Demyelinating Disease 50 0.758
415
ADN001 Adenosine Deaminase Deficiency 59 0.758
416
c SVR003 Severe Congenital Neutropenia 59 0.745
417
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.745
418
ALB002 Albinism 47 0.745
420
GRW007 Growth Hormone Deficiency 47 0.743
421
PRN029 Parainfluenza Virus Type 3 32 0.743
422
c INH030 Inherited Retinal Disorder 28 0.743
423
P MCH002 Machado-Joseph Disease 63 0.736
424
PRM163 Primary Mediastinal Large B-Cell Lymphoma 40 0.736
425
P MTH007 Methemoglobinemia 46 0.733
426
PRP016 Paraplegia 52 0.733
427
P FTL001 Fetal Alcohol Syndrome 55 0.727
428
P MLT074 Multiple Endocrine Neoplasia 58 0.727
429
P RNL017 Renal Oncocytoma 54 0.725
430
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.725
431
c MCR112 Microvascular Complications of Diabetes 2 42 0.711
432
HSH003 Hashimoto Thyroiditis 60 0.711
433
HRP009 Herpes Simplex Encephalitis 58 0.711
434
P MMB011 Membranous Nephropathy 50 0.710
435
c WLM013 Wilms Tumor 1 65 0.710
436
PRM236 Primary Biliary Cholangitis 62 0.710
437
CCN002 Cocaine Abuse 49 0.707
438
c SPN225 Spondyloarthropathy 1 70 0.703
439
c NRF024 Neurofibromatosis, Type I 76 0.703
440
c CHL119 Cholangitis, Primary Sclerosing 57 0.703
441
SPN051 Spondylitis 51 0.703
442
P SCL009 Sclerosing Cholangitis 46 0.703
443
INF009 Inflammatory Spondylopathy 30 0.703
444
PLC005 Placental Insufficiency 56 0.703
445
FDL002 Food Allergy 47 0.703
446
HDN002 Head Injury 44 0.703
447
PRL017 Prolymphocytic Leukemia 47 0.690
448
P FML011 Familial Adenomatous Polyposis 71 0.690
449
HYP458 Hyper Ige Syndrome 60 0.687
450
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.687
451
P MCR129 Microvascular Complications of Diabetes 1 68 0.685
452
c CNG223 Congenital Methemoglobinemia 39 0.685
453
SPS057 Spasticity 43 0.682
454
P HNT016 Huntington Disease 73 0.679
455
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.669
456
BBS001 Babesiosis 49 0.669
457
NRM001 Neuromyelitis Optica 60 0.669
458
HYP781 Hypoascorbemia 52 0.665
459
HND002 Hand, Foot and Mouth Disease 50 0.651
460
SVR001 Severe Acute Respiratory Syndrome 68 0.648
461
CHL028 Childhood Type Dermatomyositis 58 0.643
462
END041 Endometrial Adenocarcinoma 63 0.643
463
GLS001 Gliosarcoma 63 0.643
464
WLL004 Wallerian Degeneration 38 0.643
465
CRB090 Cerebral Hypoxia 42 0.643
466
OCL022 Ocular Melanoma 54 0.639
467
P CHN059 Chondrocalcinosis 51 0.635
468
MRK001 Merkel Cell Carcinoma 65 0.635
469
c ANM038 Anemia, Autoimmune Hemolytic 63 0.609
470
c PRG020 Paragangliomas 3 39 0.609
471
DSS009 Disseminated Intravascular Coagulation 56 0.609
472
CRV002 Cervix Uteri Carcinoma in Situ 48 0.609
473
CRV045 Cervical Intraepithelial Neoplasia 38 0.609
474
PRT058 Pure Autonomic Failure 58 0.609
475
CNN001 Cannabis Dependence 38 0.605
476
CNN002 Cannabis Abuse 44 0.605
477
ADR005 Adrenal Carcinoma 61 0.602
478
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.602
479
P HRS035 Hirschsprung Disease 1 66 0.601
480
P MSC003 Muscular Atrophy 52 0.532
481
PFF001 Pfeiffer Syndrome 77 0.527
482
SLR001 Sialuria 48 0.522
483
P BNG032 Benign Mesothelioma 53 0.504
484
PPL022 Papilloma 53 0.500
485
SQM002 Squamous Cell Papilloma 45 0.480
486
MYC005 Myocardial Stunning 45 0.480
487
ACT003 Acute Kidney Tubular Necrosis 46 0.474
488
EMB004 Embryonal Carcinoma 55 0.470
489
P CRD246 Cardiovascular System Disease 55 0.457
490
P MDL005 Medulloblastoma 75 0.448
491
P KLZ004 Kala-Azar 1 41 0.438
492
LSH001 Leishmaniasis 63 0.438
493
P FRS004 Free Sialic Acid Storage Disorders 41 0.432
494
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.428
495
CHR177 Chromophobe Renal Cell Carcinoma 54 0.414
496
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.412
497
P MLT020 Multiple Sclerosis 79 0.392
498
c BTT014 Beta-Thalassemia 72 0.391
499
YLL002 Yellow Fever 61 0.389
500
GLM044 Glomerular Disease 34 0.389
501
c GLL024 Gallbladder Disease 1 53 0.384
502
P KDN017 Kidney Cancer 60 0.375
503
c ATS007 Autism Spectrum Disorder 72 0.372
504
P TMR010 Tumor Predisposition Syndrome 69 0.369
505
P AGM001 Agammaglobulinemia 67 0.365
506
P ATR005 Atrophic Gastritis 50 0.365
507
TRD006 Tardive Dyskinesia 53 0.360
508
OTT002 Otitis Media 71 0.359
509
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.359
510
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.351
511
INH023 Inherited Cancer-Predisposing Syndrome 53 0.351
512
P ATS364 Autism 72 0.346
513
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.346
514
CHR178 Chromosomal Triplication 34 0.346
515
P ALP008 Alopecia 53 0.346
516
P PRN023 Prion Disease 60 0.344
517
c MST023 Mesothelioma, Malignant 56 0.343
518
P RBL001 Rubella 58 0.343
519
NNK001 Nonaka Myopathy 58 0.339
520
P DMN002 Dementia 65 0.332
521
P SML001 Small Cell Carcinoma 52 0.326
522
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 0.326
523
P CND004 Candidiasis 57 0.326
524
BRN018 Borna Disease 36 0.326
525
ENT004 Enthesopathy 51 0.326
526
c CNG209 Congenital Disorder of Glycosylation, Type Iif 43 0.319
527
P MMP001 Mumps 56 0.319
528
IGG001 Iga Glomerulonephritis 50 0.319
529
MYP120 Myopathy, Distal, with Rimmed Vacuoles 33 0.318
530
P MYT002 Myotonic Dystrophy 51 0.318
531
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.309
532
CRL001 Cerulean Cataract 26 0.309
533
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.307
534
RBS001 Rabies 58 0.307
535
MCS002 Mucositis 55 0.301
536
FND002 Fundus Dystrophy 55 0.301
537
CHR066 Chronic Fatigue Syndrome 60 0.301
538
c HPT007 Hepatitis E 50 0.292
539
CHL045 Choline Deficiency Disease 39 0.292
540
P SLP005 Sleep Disorder 62 0.292
541
CND006 Candida Glabrata 29 0.285
542
c ACT068 Acute Cystitis 61 0.285
543
HMG005 Hemoglobinopathy 55 0.285
544
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.285
545
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.285
546
ENT011 Enterocolitis 55 0.284
547
STT041 Stuttering 52 0.284
548
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 0.284
549
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.284
550
P URN019 Urinary Tract Infection 49 0.284
551
CNG017 Congenital Nonspherocytic Hemolytic Anemia 34 0.284
552
AMN001 Amenorrhea 53 0.284
553
HMS001 Hemosiderosis 48 0.284
554
MSN004 Mesenchymal Cell Neoplasm 42 0.284
555
DHY008 Dihydroxyadeninuria 24 0.284
556
P RRH023 Rare Hereditary Hemochromatosis 53 0.284
557
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.265
558
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.265
559
HMP005 Hemiplegia 53 0.265
560
CYT005 Cytomegalovirus Retinitis 50 0.265
561
CRY005 Cryptococcosis 61 0.265
562
PSY004 Psychotic Disorder 66 0.265
563
P BRN022 Bronchiectasis 59 0.265
564
PLC008 Placenta Disease 49 0.265
565
c BCT013 Bacterial Pneumonia 47 0.265
566
PRN019 Perinatal Necrotizing Enterocolitis 60 0.265
567
c OVR114 Ovarian Cancer 1 60 0.259
568
c SPN294 Spinocerebellar Ataxia 1 53 0.259
569
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.259
570
PRM329 Premature Aging 36 0.259
571
c FNC027 Fanconi Anemia, Complementation Group a 81 0.258
572
P LYM033 Lymphoproliferative Syndrome 59 0.258
573
P NMN002 Niemann-Pick Disease 60 0.258
574
EHR002 Ehrlichiosis 39 0.258
575
NDL024 Nodal Marginal Zone Lymphoma 37 0.243
576
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.243
577
P CCK001 Cockayne Syndrome 68 0.243
578
P ESN008 Eosinophilic Pneumonia 50 0.243
579
c CHR418 Chronic Leukemia 48 0.243
580
BLR008 Bilirubin Metabolic Disorder 57 0.243
581
PRP030 Purpura 54 0.243
582
VSC003 Visceral Leishmaniasis 54 0.243
583
KRT006 Keratoconjunctivitis 53 0.243
584
DFF036 Differentiated Thyroid Carcinoma 51 0.243
585
P MPL001 Maple Syrup Urine Disease 69 0.225
586
IMM154 Immunoglobulin a Deficiency 1 45 0.225
587
KRT009 Keratosis 52 0.225
588
PNM008 Pneumothorax 54 0.225
589
SLC006 Silicosis 55 0.225
590
LST001 Listeriosis 59 0.225
591
INT075 Intracranial Hypertension 52 0.225
592
c HMG003 Hemoglobin E Disease 41 0.225
593
LGN006 Legionnaire Disease 52 0.217
594
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.217
595
MNN009 Meningoencephalitis 48 0.217
596
P RCT021 Rectum Cancer 54 0.217
597
c HRD010 Hereditary Spastic Paraplegia 65 0.217
598
P OLG002 Oligodendroglioma 66 0.217
599
VGN023 Vaginitis 56 0.217
600
P TRT010 Teratoma 50 0.217
601
P GLL018 Gallbladder Cancer 53 0.217
602
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.217
603
SPP011 Suppression of Tumorigenicity 12 61 0.217
604
SFT003 Soft Tissue Sarcoma 57 0.217
605
CRY010 Cryptophthalmos 25 0.217
606
ESN011 Eisenmenger Syndrome 46 0.217
607
MLL001 Molluscum Contagiosum 48 0.217
608
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.183
609
GLC096 Galactorrhea 40 0.183
610
OBN001 Ouabain Resistance 15 0.183
611
P MSC002 Muscular Dystrophy-Dystroglycanopathy 37 0.183
612
FTL006 Fetal Alcohol Spectrum Disorder 43 0.183
613
HPT046 Hepatic Veno-Occlusive Disease 55 0.183
614
P END033 Endocarditis 58 0.183
615
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.183
616
P HYP058 Hypervitaminosis a 47 0.183
617
MCS004 Mucosal Melanoma 46 0.183
618
STR103 Streptococcus Pneumonia 47 0.183
619
c MCR312 Microphthalmia, Syndromic 10 39 0.183
620
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 64 0.183
621
INF159 Infantile Sialic Acid Storage Disease 41 0.183
622
c HPT003 Hepatitis a 63 0.183
623
CMM005 Common Cold 55 0.183
624
TCL003 T Cell Deficiency 44 0.183
625
CRB037 Cerebral Palsy 67 0.183
626
QDR001 Quadriplegia 49 0.183
627
TYP007 Typhoid Fever 63 0.183
628
FCL012 Facial Paralysis 49 0.183
629
CPL003 Capillary Leak Syndrome 54 0.183
630
HMN048 Human Papillomavirus Infectious Disease 46 0.183
631
LYM009 Lymphocytic Choriomeningitis 46 0.183
632
P CNT005 Central Nervous System Lymphoma 51 0.183
633
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.183
634
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.183
635
c JVN010 Juvenile Rheumatoid Arthritis 66 0.183
636
HYP264 Hypertonia 36 0.183
637
PRM226 Primary Central Nervous System Lymphoma 47 0.183
638
MLG079 Malignant Pleural Mesothelioma 42 0.183
639
PLM035 Pulmonary Eosinophilia 49 0.183
640
CTN007 Cutaneous Leishmaniasis 61 0.183
641
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 0.183
642
P AVS003 Avascular Necrosis 41 0.183
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