Search results for brilliant blue G

682 hits were found for brilliant blue G

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 65 42.671
2
DFC004 Deficiency Anemia 74 30.170
3
P BRS047 Breast Cancer 98 29.889
4
MCL003 Macular Holes 44 26.709
5
RPD005 Rapidly Involuting Congenital Hemangioma 46 26.216
6
48X005 48,xyyy 39 26.027
7
PRT251 Proteinuria, Chronic Benign 57 25.479
8
c LKM061 Leukemia, Acute Myeloid 83 24.459
9
P NRB001 Neuroblastoma 66 24.425
10
HLX001 Helix Syndrome 48 24.209
11
STM007 Stomatitis 54 24.046
12
P MLN008 Melanoma 76 23.633
13
CHL014 Cholera 62 23.431
14
P THL005 Thalassemia 56 23.206
15
IRN002 Iron Metabolism Disease 57 22.919
16
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 22.918
17
P LKM002 Leukemia 67 22.701
18
P MYL006 Myeloid Leukemia 61 22.413
19
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 22.244
20
MYL069 Myeloma, Multiple 77 22.175
22
PST092 Posttransplant Acute Limbic Encephalitis 28 21.736
23
P CTR002 Cataract 60 21.614
24
ISC004 Ischemia 61 21.065
25
TXC005 Toxic Shock Syndrome 62 20.792
26
CLT003 Colitis 63 20.581
27
c HYP836 Hypercholesterolemia, Familial, 1 73 20.136
28
ULC004 Ulcerative Colitis 74 20.008
29
P PRD008 Periodontitis 64 19.976
30
P BLD134 Bladder Cancer 79 19.892
31
c CHR684 Chronic Kidney Disease 69 19.837
32
ARG004 Argyria 26 18.995
33
47X002 47,xyy 48 18.904
34
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 18.822
35
MYL009 Myelodysplastic Syndrome 67 18.811
36
GLL048 Glial Tumor 52 18.691
37
c MCR115 Microvascular Complications of Diabetes 5 65 18.648
38
CYT002 Cytokine Deficiency 43 18.605
39
P GRF003 Graft-Versus-Host Disease 71 18.330
40
END057 Endometrial Cancer 72 18.294
41
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 18.290
42
GLM045 Glioma 63 18.228
43
P HPT021 Hepatitis 69 18.192
44
CRV035 Cervical Cancer 73 18.123
45
BCT022 Bacterial Infectious Disease 56 18.067
46
HMN044 Human Immunodeficiency Virus Type 1 78 18.019
47
P OVR042 Ovarian Cancer 88 17.810
48
P THR014 Thrombocytopenia 66 17.735
49
c BRN108 Branchiootic Syndrome 1 62 17.282
50
P GST044 Gastritis 55 17.261
51
P DRR001 Diarrhea 55 17.167
52
P LKM062 Leukemia, Acute Lymphoblastic 69 17.146
53
PST011 Pustulosis of Palm and Sole 52 17.088
54
P PSR002 Psoriasis 63 17.075
55
P RTN008 Retinitis Pigmentosa 80 17.054
56
P LVR013 Liver Disease 69 16.893
57
HRW001 Hair Whorl 35 16.892
58
GLB002 Glioblastoma 67 16.879
59
c AMY091 Amyotrophic Lateral Sclerosis 1 88 16.842
60
ALL029 Allergic Disease 59 16.829
61
LYM133 Lymphoma, Hodgkin, Classic 74 16.796
62
c BTT014 Beta-Thalassemia 72 16.784
63
OST159 Osteogenic Sarcoma 66 16.778
64
P HRT032 Heart Disease 81 16.691
65
CYS001 Cystic Fibrosis 78 16.687
66
P LPS004 Lupus Erythematosus 61 16.657
67
P PRS040 Prostate Cancer 95 16.652
68
MLR004 Malaria 80 16.476
69
AGN016 Aging 54 16.393
70
P RTN024 Retinoblastoma 73 16.385
71
CRH001 Crohn's Disease 80 16.343
72
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 16.322
73
DRM006 Dermatitis 62 16.313
74
P PNC035 Pancreatic Cancer 86 16.156
75
BRN071 Brain Injury 50 16.124
76
P INF032 Infertility 57 16.068
77
P LNG032 Lung Cancer 98 16.016
78
HYP066 Hyperglycemia 61 15.984
79
P GLM007 Glomerulonephritis 60 15.983
80
P ALZ034 Alzheimer Disease 87 15.961
81
SPN186 Spinal Cord Injury 61 15.956
82
RTN017 Retinal Detachment 60 15.943
83
HYP056 Hypoglycemia 65 15.925
84
P HRP006 Herpes Simplex 65 15.876
85
LPP008 Lipoprotein Quantitative Trait Locus 65 15.823
86
NNL005 Non-Alcoholic Fatty Liver Disease 63 15.812
87
P HPT023 Hepatocellular Carcinoma 96 15.789
88
P ADN016 Adenocarcinoma 63 15.741
89
HYP266 Hypoxia 57 15.633
90
FTT001 Fatty Liver Disease 62 15.614
91
P HML002 Hemolytic Anemia 62 15.573
92
ART140 Arteries, Anomalies of 53 15.521
93
P BCL017 B-Cell Lymphoma 59 15.488
94
PRT036 Peritonitis 65 15.352
95
BRN004 Brain Edema 54 15.307
96
c SYS001 Systemic Lupus Erythematosus 87 15.278
97
c MCR113 Microvascular Complications of Diabetes 3 52 15.260
98
P ACN011 Acne 57 15.180
99
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 15.164
100
c MCR120 Microvascular Complications of Diabetes 7 47 15.084
101
PPL052 Papillomatosis, Confluent and Reticulated 34 15.041
102
SPL018 Splenomegaly 49 15.039
103
P ENC018 Encephalopathy 62 14.974
104
P VSC007 Vascular Disease 63 14.949
105
P PNC044 Pancreatitis 61 14.879
106
LPD008 Lipid Metabolism Disorder 62 14.878
107
CRB004 Cerebral Artery Occlusion 45 14.838
108
c HPT073 Hepatitis C Virus 71 14.820
109
NRR001 Neuroretinitis 42 14.787
110
c MCR133 Microvascular Complications of Diabetes 4 41 14.712
111
c MCR130 Microvascular Complications of Diabetes 6 41 14.707
112
P RHM011 Rheumatoid Arthritis 82 14.652
113
P MYC007 Myocardial Infarction 70 14.627
114
c LKM063 Leukemia, Chronic Myeloid 71 14.619
115
P NRP001 Neuropathy 60 14.559
116
IRN001 Iron Deficiency Anemia 58 14.550
117
ATM095 Autoimmune Disease 61 14.476
118
ENT011 Enterocolitis 55 14.468
119
END086 End Stage Renal Disease 52 14.458
120
c HPT016 Hepatitis B 62 14.372
121
BRT054 Brittle Bone Disorder 74 14.372
122
P HYP069 Hyperparathyroidism 62 14.369
123
c HPT001 Hepatitis C 62 14.348
124
SVR004 Severe Combined Immunodeficiency 72 14.277
125
P LTR001 Lateral Sclerosis 58 14.249
126
RTN023 Retinitis 46 14.208
127
P CRD119 Cardiac Arrest 67 14.160
128
P MJR001 Major Depressive Disorder 68 14.128
129
ALC007 Alcohol Dependence 66 14.097
130
BNR002 Bone Resorption Disease 47 14.097
131
TRM010 Traumatic Brain Injury 51 14.056
132
P SYP003 Syphilis 59 14.010
133
P AMY004 Amyloidosis 70 13.975
134
STR067 Stroke, Ischemic 80 13.890
135
c ACT071 Acute Kidney Failure 60 13.826
136
P LKM071 Leukemia, Chronic Lymphocytic 75 13.803
137
P MYP004 Myopathy 67 13.774
138
RBS001 Rabies 58 13.745
139
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 13.721
140
ATH013 Atherosclerosis Susceptibility 63 13.710
141
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 13.695
142
CNS004 Constipation 56 13.653
143
P DRM053 Dermatitis, Atopic 65 13.630
144
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 13.575
145
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 13.569
146
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 13.565
147
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 13.565
148
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 13.563
149
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 13.563
150
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 13.563
151
P HYP086 Hypothyroidism 69 13.549
152
P BPL003 Bipolar Disorder 56 13.476
153
DPR016 Depression 65 13.452
154
GST045 Gastroenteritis 58 13.447
155
c MJR022 Major Affective Disorder 8 38 13.427
156
c MJR024 Major Affective Disorder 9 41 13.427
157
P URN019 Urinary Tract Infection 49 13.412
158
PLM129 Pulmonary Disease, Chronic Obstructive 74 13.300
159
P RTN016 Retinal Degeneration 52 13.277
160
CHL123 Chlamydia 58 13.173
161
THY029 Thyroid Carcinoma 51 13.151
162
SKN016 Skin Disease 63 13.125
163
P NPH012 Nephrotic Syndrome 60 13.122
164
P MYP006 Myopia 56 13.117
165
HLC007 Helicobacter Pylori Infection 67 13.104
166
P AST005 Asthma 76 12.814
167
P PHC003 Pheochromocytoma 69 12.781
168
MDD011 Mood Disorder 62 12.725
169
P END033 Endocarditis 58 12.689
170
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 12.641
171
c ACT073 Acute Leukemia 58 12.557
172
BRN024 Bronchitis 67 12.556
173
P ALC033 Alcohol Use Disorder 61 12.516
174
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 12.515
175
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 12.443
176
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 12.443
177
P OST002 Osteoporosis 76 12.439
178
CNT047 Contact Dermatitis 57 12.388
179
LNG099 Lung Disease 62 12.366
180
P HYP750 Hypertriglyceridemia, Familial 62 12.348
181
P MYC084 Mycobacterium Tuberculosis 1 68 12.328
182
HMS001 Hemosiderosis 48 12.316
183
P LNG064 Lung Cancer Susceptibility 3 70 12.266
184
P EYD002 Eye Disease 57 12.202
185
TTN003 Tetanus 65 12.200
186
KRT009 Keratosis 53 12.189
187
P RHB003 Rhabdomyosarcoma 66 12.167
188
c BSL007 Basal Cell Carcinoma 68 12.150
189
P RHN004 Rhinitis 57 12.090
190
CNG034 Congestive Heart Failure 69 12.038
191
DSS032 Disease by Infectious Agent 55 11.998
192
P RTN018 Retinal Disease 53 11.960
193
PLM010 Pulmonary Edema 55 11.895
194
P CHR345 Chronic Pain 50 11.734
195
c ACT075 Acute Myocardial Infarction 56 11.575
196
P GLM040 Glioma Susceptibility 1 71 11.558
197
P RRH023 Rare Hereditary Hemochromatosis 54 11.531
198
CVD001 Covid-19 57 11.530
199
PNG002 Pain Agnosia 51 11.527
200
P RCT021 Rectum Cancer 54 11.521
201
P MSC005 Muscular Dystrophy 67 11.518
202
ATS010 Autosomal Recessive Disease 42 11.510
203
MST005 Mastitis 53 11.481
204
P PRP019 Peripheral Nervous System Disease 58 11.390
205
VCC001 Vaccinia 47 11.364
206
c PRD040 Periodontitis, Chronic 52 11.341
207
OCL069 Ocular Motor Apraxia 57 11.324
208
c PCH010 Pachyonychia Congenita 3 43 11.318
209
P HYP098 Hypereosinophilic Syndrome 66 11.239
210
KPS004 Kaposi Sarcoma 77 11.177
211
c DWL002 Dowling-Degos Disease 1 58 11.168
212
DSS008 Disease of Mental Health 74 11.163
213
c ALP101 Alpha-Thalassemia 62 11.119
214
OST017 Osteomyelitis 63 11.113
215
BCK006 Back Pain 47 11.105
216
c ACT135 Acute Graft Versus Host Disease 51 11.077
217
P GRV001 Graves' Disease 55 10.958
218
P THY032 Thyroiditis 57 10.946
219
P TRM003 Tremor 48 10.907
220
P SCK005 Sickle Cell Disease 56 10.880
221
P URT039 Urticaria 58 10.876
222
PNM008 Pneumothorax 54 10.850
223
c MGR028 Migraine with or Without Aura 1 64 10.846
224
P INF038 Influenza 68 10.800
225
c FML021 Familial Hypercholesterolemia 72 10.795
226
P HYP076 Hyperthyroidism 53 10.782
227
P CND004 Candidiasis 58 10.730
228
P CYS018 Cystitis 59 10.707
229
P INS002 in Situ Carcinoma 53 10.656
230
P KLZ004 Kala-Azar 1 41 10.621
231
LSH001 Leishmaniasis 64 10.621
232
IGG001 Iga Glomerulonephritis 50 10.618
233
RCK004 Rickets 68 10.614
234
MTB004 Metabolic Acidosis 48 10.603
235
CHR178 Chromosomal Triplication 34 10.596
236
MSC157 Muscular Dystrophy, Duchenne Type 79 10.478
237
ACT119 Acute Promyelocytic Leukemia 62 10.443
238
P MNN013 Meningitis 65 10.431
239
ALL003 Allergic Rhinitis 67 10.406
240
P ATT013 Attention Deficit-Hyperactivity Disorder 64 10.325
241
P EPL164 Epilepsy 68 10.320
242
PPT005 Peptic Ulcer Disease 58 10.291
243
NRL016 Neural Tube Defects 81 10.291
244
P ALP008 Alopecia 54 10.291
245
P OVR082 Overgrowth Syndrome 49 10.271
246
P PLM036 Pulmonary Fibrosis 66 10.229
247
HYP060 Hyperinsulinism 54 10.178
248
OTT002 Otitis Media 71 10.166
249
P MDL005 Medulloblastoma 75 10.128
250
ANX004 Anoxia 40 10.096
251
BRK010 Burkitt Lymphoma 66 10.089
252
P BNG032 Benign Mesothelioma 53 10.072
253
ADR040 Adrenal Gland Pheochromocytoma 46 10.029
254
c SCL052 Scleroderma, Familial Progressive 61 10.004
255
P PTN014 Patent Ductus Arteriosus 1 59 9.953
256
MSL001 Measles 61 9.933
257
PRP027 Peripheral Vascular Disease 71 9.931
258
P NSP012 Nasopharyngeal Carcinoma 61 9.902
259
GST023 Gastric Ulcer 52 9.875
260
c DNT047 Dentinogenesis Imperfecta Type 2 35 9.839
261
GTR002 Goiter 53 9.825
262
P SNS001 Sensorineural Hearing Loss 59 9.750
263
HMP009 Haemophilus Influenzae 41 9.727
264
ANX010 Anxiety 70 9.724
265
P UVT001 Uveitis 57 9.723
266
P BND020 Bone Disease 59 9.692
267
DNT012 Dental Caries 53 9.683
268
MCL006 Macular Retinal Edema 57 9.658
269
MLG169 Malignant Astrocytoma 57 9.603
270
TRY001 Trypanosomiasis 50 9.544
271
SCH014 Schistosomiasis 56 9.532
272
SCK003 Sickle Cell Anemia 74 9.499
273
PTH003 Pathologic Nystagmus 52 9.495
274
P FBR017 Fibrosarcoma 56 9.432
275
GST019 Gastrointestinal Stromal Tumor 78 9.327
276
P PRK057 Parkinson Disease, Late-Onset 80 9.268
277
PRT013 Portal Hypertension 59 9.148
278
P HYD006 Hydrocephalus 61 9.142
279
DPH001 Diphtheria 59 9.109
280
PLM033 Pulmonary Embolism 58 9.087
281
c ATS007 Autism Spectrum Disorder 72 9.079
282
P VTR007 Vitreoretinopathy 46 9.079
283
P CLC063 Celiac Disease 1 66 9.058
284
SLP001 Sleeping Sickness 56 9.035
285
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 9.013
286
P END047 Endophthalmitis 53 9.010
287
PPL022 Papilloma 53 8.979
288
P SYS005 Systemic Scleroderma 74 8.955
289
OCL006 Ocular Hypertension 53 8.954
290
PLY150 Polykaryocytosis Inducer 29 8.908
291
PHR003 Pharyngitis 58 8.883
292
P HDC001 Headache 57 8.879
293
GNG013 Gingivitis 59 8.876
294
P RBL001 Rubella 58 8.858
295
INF034 Infective Endocarditis 54 8.853
296
HMG005 Hemoglobinopathy 56 8.763
297
ALL014 Allergic Encephalomyelitis 34 8.729
298
PHN003 Phenylketonuria 76 8.649
299
P HNT016 Huntington Disease 73 8.587
300
KRT019 Keratitis, Hereditary 66 8.550
301
P MCR129 Microvascular Complications of Diabetes 1 68 8.516
302
c SPN225 Spondyloarthropathy 1 70 8.500
303
CHC001 Chickenpox 57 8.487
304
SPN051 Spondylitis 51 8.483
305
INF009 Inflammatory Spondylopathy 30 8.483
306
FND002 Fundus Dystrophy 55 8.465
307
HYP080 Hypogonadism 50 8.432
308
ALL006 Allergic Asthma 56 8.427
309
CHR074 Choriocarcinoma 46 8.421
310
LPT014 Leptin Deficiency or Dysfunction 78 8.421
311
CHG001 Chagas Disease 66 8.371
312
IMP005 Impotence 52 8.367
313
NRT004 Neuritis 53 8.365
314
P MSC003 Muscular Atrophy 52 8.362
315
ADL002 Adult Syndrome 70 8.292
316
P PLY019 Polyneuropathy 52 8.286
317
P MYC008 Myocarditis 59 8.269
318
MSC007 Muscle Hypertrophy 64 8.260
319
TYP007 Typhoid Fever 64 8.233
320
ANG054 Angina Pectoris 66 8.232
321
NNL006 Non-Alcoholic Steatohepatitis 54 8.217
322
c PLM164 Pulmonary Hypertension, Primary, 1 76 8.209
323
MNN043 Meningioma, Familial 79 8.123
325
c MCR112 Microvascular Complications of Diabetes 2 42 8.075
326
ACR007 Acromegaly 70 8.001
327
URM002 Uremia 47 7.995
328
GT001 Gout 64 7.985
329
P ASP006 Aspergillosis 72 7.974
330
CMB007 Combined Immunodeficiency 57 7.915
331
BRC012 Brucellosis 66 7.914
332
FRN006 Frontotemporal Dementia 68 7.907
333
ALB002 Albinism 47 7.875
334
ALL010 Allergic Contact Dermatitis 56 7.870
335
PNC129 Pancreatic Adenocarcinoma 65 7.865
336
PST028 Post-Traumatic Stress Disorder 59 7.837
337
P PLY018 Polycythemia 56 7.813
338
PRM236 Primary Biliary Cholangitis 60 7.806
339
MTH009 Mouth Disease 57 7.789
340
P HYP265 Hypotonia 42 7.787
341
HRT011 Heart Septal Defect 49 7.766
342
CRH005 Crohn's Colitis 53 7.759
343
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 7.753
344
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 7.753
345
CLN015 Colon Adenocarcinoma 65 7.721
346
THY030 Thyroid Gland Disease 50 7.719
347
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 7.710
348
P TTR001 Tetralogy of Fallot 69 7.705
349
P PYL005 Pyelonephritis 57 7.691
350
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 7.628
351
P VNT002 Ventricular Septal Defect 58 7.623
352
MLD018 Mild Cognitive Impairment 48 7.611
353
P PRK039 Parkinsonism 55 7.604
354
MCR013 Microphthalmia 60 7.596
355
P BRN022 Bronchiectasis 60 7.571
356
P KDN017 Kidney Cancer 61 7.561
357
ENT004 Enthesopathy 51 7.548
358
LYM027 Lymphopenia 56 7.534
359
LBR036 Leber Plus Disease 66 7.508
360
SYN036 Syncope 45 7.497
361
NWC001 Newcastle Disease 47 7.493
362
P SLM003 Salmonellosis 54 7.431
363
P SLP005 Sleep Disorder 61 7.417
364
PLS007 Plasmodium Falciparum Malaria 52 7.413
365
SQM002 Squamous Cell Papilloma 46 7.396
366
URT001 Urethritis 53 7.319
367
ACT098 Acute Erythroid Leukemia 55 7.292
368
DYS015 Dysentery 50 7.278
369
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 7.223
370
P CRV039 Cervicitis 52 7.198
371
P ANT006 Antiphospholipid Syndrome 55 7.159
372
NPH009 Nephrolithiasis 54 7.127
373
P SML001 Small Cell Carcinoma 52 7.124
374
P ATR011 Atrial Fibrillation 66 7.122
375
PLS011 Plasmacytoma 56 7.122
376
P CLR019 Color Blindness 48 7.116
377
P STR020 Strabismus 56 7.111
378
DMY004 Demyelinating Disease 50 7.097
379
ANT024 Anthrax Disease 58 7.073
380
P NMN002 Niemann-Pick Disease 60 7.050
381
P SLP006 Sleep Apnea 69 7.040
382
PLG002 Plague 58 7.039
383
AST006 Astigmatism 47 6.987
384
FDL002 Food Allergy 47 6.967
385
BRN028 Brain Cancer 74 6.910
386
SCR001 Secretory Meningioma 40 6.899
387
LYM002 Lymphoplasmacyte-Rich Meningioma 35 6.899
388
SPN021 Spinal Meningioma 50 6.899
389
CLR033 Color Vision Deficiency 40 6.848
390
MYL031 Myeloproliferative Neoplasm 66 6.813
391
VSC003 Visceral Leishmaniasis 55 6.791
392
P CRN025 Corneal Dystrophy 49 6.788
393
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 6.779
394
c LKM005 Leukemia, T-Cell, Chronic 34 6.767
395
AMN001 Amenorrhea 54 6.748
396
MCH006 Mechanical Strabismus 40 6.715
397
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 6.702
398
P PRP029 Porphyria 60 6.694
399
P WRD001 Waardenburg's Syndrome 60 6.671
400
DMP001 Dumping Syndrome 43 6.667
401
PLM031 Poliomyelitis 63 6.648
402
URT010 Ureteral Obstruction 45 6.608
403
HYD002 Hydronephrosis 58 6.514
404
P TBR001 Tuberous Sclerosis 69 6.473
405
OST003 Osteonecrosis 61 6.468
406
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 6.443
407
c ACT004 Acute Diarrhea 40 6.419
408
VTR003 Vitreous Detachment 41 6.330
409
PSR001 Psoriatic Arthritis 62 6.312
410
EXP004 Exophthalmos 51 6.303
411
P INT070 Intestinal Obstruction 57 6.300
412
ART002 Arts Syndrome 66 6.287
413
c GLL024 Gallbladder Disease 1 52 6.283
414
RTN002 Retinal Perforation 37 6.253
415
SPP011 Suppression of Tumorigenicity 12 61 6.236
416
P CRN026 Corneal Edema 42 6.196
417
PMP014 Pemphigoid 51 6.192
418
P ART023 Arthropathy 61 6.164
419
SYN007 Synovitis 55 6.142
420
GLM044 Glomerular Disease 35 6.071
421
P END046 Endometritis 46 6.063
422
CHR100 Chronic Ulcer of Skin 57 6.039
423
c BCT007 Bacterial Meningitis 55 6.031
424
STT001 Status Epilepticus 59 6.014
425
PLC002 Plica Syndrome 35 6.010
426
P KRT007 Keratoconus 50 5.947
427
ASY002 Asymptomatic Neurosyphilis 41 5.937
428
NRS003 Neurosyphilis 45 5.937
429
P HRS035 Hirschsprung Disease 1 66 5.903
430
CRT015 Carotid Artery Occlusion 45 5.891
431
DBT010 Diabetic Neuropathy 54 5.783
432
ANT018 Anthracosis 51 5.737
433
P ANG015 Angioedema 56 5.733
434
PRC003 Proctitis 49 5.726
435
c HNT011 Huntington Disease-Like 3 34 5.724
436
HRT012 Heart Valve Disease 53 5.721
437
P PRN023 Prion Disease 60 5.688
438
ACT084 Acute Stress Disorder 54 5.669
439
HND015 Hand Skill, Relative 30 5.647
440
c GRV008 Graves Disease 1 54 5.645
441
WLS001 Wilson Disease 70 5.644
442
ERY004 Erysipelas 47 5.643
443
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 5.634
444
P HRD011 Hereditary Spherocytosis 64 5.602
445
ING001 Inguinal Hernia 59 5.601
446
APH002 Aphasia 56 5.598
447
P VNW001 Von Willebrand's Disease 65 5.587
448
CHL067 Cholecystitis 60 5.584
449
LPT001 Leptospirosis 66 5.578
450
RHM028 Rheumatic Heart Disease 56 5.504
451
P LRY044 Larynx Cancer 54 5.499
452
P LKD001 Leukodystrophy 59 5.477
453
CND006 Candida Glabrata 30 5.467
454
P PNM006 Pneumoconiosis 55 5.458
455
PFF001 Pfeiffer Syndrome 77 5.425
456
c FNC043 Fanconi Anemia, Complementation Group E 62 5.407
457
STN013 Stenotrophomonas Maltophilia Infection 26 5.405
458
c HNT004 Huntington Disease-Like 2 52 5.399
459
SCT002 Scotoma 42 5.381
460
CRV002 Cervix Uteri Carcinoma in Situ 47 5.379
461
CRV045 Cervical Intraepithelial Neoplasia 39 5.379
462
KRT008 Keratopathy 46 5.378
463
THR016 Thrombophlebitis 50 5.357
464
RNL077 Renal Fibrosis 46 5.283
465
DRM011 Dermatophytosis 52 5.276
466
NRN004 Neuroendocrine Tumor 59 5.267
467
ECT026 Ectopic Pregnancy 48 5.254
468
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 5.245
469
P SPN046 Spinal Muscular Atrophy 63 5.178
470
PRR004 Preretinal Fibrosis 34 5.169
471
ALK013 Alkaptonuria 59 5.162
472
P DMY001 Demyelinating Polyneuropathy 41 5.156
473
NPH091 Nephrolithiasis, Calcium Oxalate 61 5.153
474
LWC001 Low Compliance Bladder 45 5.150
475
YLL002 Yellow Fever 61 5.087
476
OST011 Osteomalacia 52 5.065
477
c INH030 Inherited Retinal Disorder 28 5.046
478
DBT006 Diabetic Macular Edema 48 5.019
479
P EHL001 Ehlers-Danlos Syndrome 58 5.002
480
SCR011 Scrapie 39 5.000
481
MMM001 Mammary Paget's Disease 53 4.984
482
P MYT002 Myotonic Dystrophy 51 4.974
483
P EMB005 Embryonal Rhabdomyosarcoma 53 4.896
484
BLD131 Bladder Urothelial Carcinoma 60 4.864
485
ATR057 Atrioventricular Block 54 4.855
486
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 4.819
487
P TMP001 Temporal Lobe Epilepsy 49 4.795
488
HYD038 Hydrops Fetalis, Nonimmune 59 4.784
489
PLR007 Pleural Empyema 51 4.776
490
FCL012 Facial Paralysis 49 4.738
491
AMB002 Amblyopia 50 4.676
492
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 4.642
493
c ALM001 Al Amyloidosis 54 4.640
494
MYC006 Mycosis Fungoides 65 4.619
495
LTN004 Late-Onset Retinal Degeneration 60 4.581
496
P MVM001 Movement Disease 61 4.579
497
SPP007 Suppression Amblyopia 38 4.544
498
SRC027 Sarcoma, Synovial 58 4.542
499
P CNT005 Central Nervous System Lymphoma 52 4.537
500
CNN003 Conn's Syndrome 79 4.533
501
PRM226 Primary Central Nervous System Lymphoma 47 4.519
502
AMN003 Amnestic Disorder 54 4.502
503
PLR008 Pleurisy 50 4.490
504
TNG007 Tongue Carcinoma 52 4.457
505
P BRC006 Brachydactyly 51 4.442
506
P HMR003 Hemorrhagic Disease 59 4.360
507
MLG079 Malignant Pleural Mesothelioma 42 4.353
508
c HPT015 Hepatitis D 49 4.351
509
FLR002 Filariasis 55 4.344
510
P MLG056 Malignant Hyperthermia 66 4.328
511
LRN003 Learning Disability 49 4.327
512
ABT001 Abetalipoproteinemia 68 4.323
513
NRT001 Neurotic Disorder 56 4.293
514
MST021 Meester-Loeys Syndrome 42 4.282
515
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 64 4.239
516
c ACT042 Acute Pyelonephritis 45 4.214
517
SLC006 Silicosis 56 4.205
518
PRT082 Preterm Premature Rupture of the Membranes 57 4.176
519
P MTR003 Mitral Valve Stenosis 53 4.162
520
THL010 Thalassemia Minor 32 4.158
521
c HMG003 Hemoglobin E Disease 42 4.151
522
P BNC003 Bone Cancer 58 4.150
523
HST011 Histoplasmosis 55 4.135
524
P HMG032 Hemoglobin H Disease 51 4.126
525
SML019 Smallpox 55 4.120
526
PRT058 Pure Autonomic Failure 58 4.111
527
P OCL002 Oculocutaneous Albinism 59 4.089
528
TST044 Testicular Torsion 45 4.070
529
APH001 Aphthous Stomatitis 58 4.062
530
HYP781 Hypoascorbemia 52 4.056
531
EPD015 Epidemic Typhus 44 4.033
532
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 4.002
533
GSG001 Gas Gangrene 52 3.972
534
P PRP003 Porphyria Cutanea Tarda 66 3.966
535
ANG011 Angiodysplasia 42 3.965
536
MLD001 Melioidosis 67 3.955
537
CRB090 Cerebral Hypoxia 42 3.954
538
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 3.912
539
P INT143 Interstitial Cystitis 60 3.896
540
P TRC031 Trichorhinophalangeal Syndrome 38 3.877
541
ALP095 Alpha Thalassemia-X-Linked Intellectual Disability Syndrome 44 3.871
542
PNM013 Pneumococcal Meningitis 43 3.869
543
URT049 Urate Oxidase, Pseudogene 24 3.868
544
DNT001 Dental Fluorosis 43 3.868
545
GNT023 Gnathostoma Infection 19 3.862
546
GNT004 Gnathomiasis 29 3.851
547
IDP091 Idiopathic Nephrotic Syndrome 47 3.847
548
QFV001 Q Fever 62 3.798
549
P HMR005 Hemorrhoid 49 3.792
550
P MGR001 Migraine Without Aura 49 3.791
551
CYS010 Cystinosis 62 3.784
552
KLB003 Klebsiella Pneumonia 50 3.733
553
GLM008 Glomus Tumor 50 3.727
554
HYP001 Hypochromic Microcytic Anemia 37 3.714
555
ERY003 Erythema Multiforme 56 3.679
556
P CYS039 Cystic Kidney Disease 53 3.678
557
CLL010 Cellular Ependymoma 57 3.671
558
GLL008 Gilles De La Tourette Syndrome 65 3.668
559
APN008 Apnea, Obstructive Sleep 67 3.637
560
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 3.637
561
PRN029 Parainfluenza Virus Type 3 32 3.584
562
P HRD012 Hereditary Elliptocytosis 55 3.551
563
P HRM001 Hermansky-Pudlak Syndrome 65 3.527
564
STC004 Stachybotrys Chartarum 33 3.450
565
c WRD030 Waardenburg Syndrome, Type 1 53 3.447
566
RCT015 Reactive Arthritis 61 3.442
567
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 3.441
568
WLL004 Wallerian Degeneration 38 3.405
569
c RNG015 Ring Chromosome 2 22 3.388
570
MCL027 Macular Dystrophy, Dominant Cystoid 51 3.379
571
TRG002 Trigeminal Neuralgia 61 3.367
572
P BNG030 Benign Ependymoma 51 3.363
573
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 3.356
574
ANK001 Ankylosis 51 3.343
575
HND002 Hand, Foot and Mouth Disease 50 3.335
576
P SLP003 Salpingitis 40 3.332
577
P HYP077 Hypertrichosis 46 3.298
578
P BRB001 Beriberi 44 3.283
579
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 3.282
580
NRG002 Neurogenic Bladder 55 3.241
581
VRL003 Variola Major 43 3.231
582
MLT157 Multiple System Atrophy 1 69 3.207
583
WLF001 Wolff-Parkinson-White Syndrome 65 3.190
584
CLB002 Clubfoot 51 3.176
585
c ATM075 Autoimmune Encephalitis 40 3.099
586
P YWS001 Yaws 36 3.097
587
BRN032 Brain Glioma 45 3.095
588
P PLL002 Pellagra 46 3.052
589
PRS042 Prostate Disease 42 3.025
590
P MTR012 Mitral Valve Disease 57 3.016
591
P DRM007 Dermatitis Herpetiformis 54 2.996
592
ACH004 Achondroplasia 66 2.954
593
THY128 Thyroid Tumor 35 2.908
594
MLT006 Multidrug-Resistant Tuberculosis 47 2.881
595
BRN026 Branch Retinal Artery Occlusion 41 2.870
596
c ATM099 Autoimmune Uveitis 45 2.870
597
PLR005 Pleuropneumonia 33 2.860
598
PTY002 Pityriasis Versicolor 38 2.834
599
CHL039 Choledocholithiasis 37 2.824
600
c OST124 Osteogenesis Imperfecta, Type V 43 2.803
601
ACT055 Actinomycosis 55 2.792
602
SNG003 Single Ventricular Heart 30 2.787
603
APR001 Apraxia 52 2.737
604
SWL001 Swallowing Disorders 38 2.715
605
CLC006 Calcinosis 47 2.709
606
P SCL015 Scleritis 48 2.684
607
P TYR004 Tyrosinemia 50 2.650
608
FBR019 Fibromatosis 42 2.649
609
c DRM040 Dermatitis Herpetiformis, Familial 35 2.647
610
c LSS005 Lissencephaly 1 57 2.636
611
DBL002 Double Outlet Right Ventricle 57 2.557
612
BRX001 Bruxism 51 2.547
613
SBC003 Subacute Bacterial Endocarditis 33 2.522
614
c MYP018 Myopia 6 27 2.508
615
EBL001 Ebola Hemorrhagic Fever 56 2.469
616
CRN027 Corneal Neovascularization 47 2.462
617
c HRD142 Hereditary Xanthinuria 43 2.453
618
CLB019 Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly 43 2.451
619
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 47 2.402
620
P ECT005 Ectropion 41 2.394
621
P AGN002 Agnosia 54 2.394
622
EPC005 Epicanthus 36 2.390
623
P RTN014 Retinal Artery Occlusion 47 2.378
624
MTG001 Metagonimiasis 24 2.375
625
DST016 Distomatosis 22 2.345
626
c SBC007 Subacute Thyroiditis 43 2.320
627
c VRL012 Viral Meningitis 46 2.315
628
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 2.288
629
PNC013 Pancreatic Ductal Carcinoma 48 2.276
630
PHS025 Phosphatase, Acid, of Tissues 28 2.244
631
ACN019 Acanthamoeba Keratitis 30 2.204
632
HTR005 Heterochromia Iridis 21 2.163
633
NST002 Nestor-Guillermo Progeria Syndrome 35 2.132
634
OPS001 Opisthorchiasis 41 2.129
635
c PRG106 Progressive Muscular Dystrophy 32 2.124
636
c TRS012 Trisomy 22 24 2.067
637
NM001 Noma 38 2.057
638
CTT001 Catatrichy 15 2.028
639
PLM070 Pulmonic Stenosis 49 2.021
640
PRP017 Periapical Periodontitis 46 1.995
641
c MCR312 Microphthalmia, Syndromic 10 40 1.958
642
c RTN058 Retinitis Pigmentosa 3 43 1.950
643
FST001 Foster-Kennedy Syndrome 39 1.926
644
ACT038 Acute Retrobulbar Neuritis 24 1.916
645
c XNT010 Xanthinuria, Type I 52 1.906
646
PNM005 Pneumonic Plague 47 1.901
647
TBL029 Tubulin, Beta 28 1.882
648
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 1.832
649
PRR015 Preauricular Fistulae, Congenital 19 1.828
650
CHN010 Chondroma 43 1.825
651
STR103 Streptococcus Pneumonia 47 1.818
652
DHY008 Dihydroxyadeninuria 24 1.808
653
ANL022 Anal Fistula 47 1.780
654
c NRD016 Neurodegeneration with Brain Iron Accumulation 6 50 1.754
655
ETH012 Ethylene Glycol Poisoning 29 1.724
656
PMP002 Pemphigoid Gestationis 38 1.719
657
NRT011 Neurotrophic Keratopathy 36 1.715
658
c WRD010 Waardenburg Syndrome Type 4 30 1.686
659
FSH001 Fish-Eye Disease 44 1.680
660
P HRD086 Hereditary Hypophosphatemic Rickets 40 1.590
661
HTR003 Heterotaxy 43 1.540
662
ADJ001 Adjustment Disorder 47 1.520
663
BLL003 Bell's Palsy 48 1.519
664
DXT001 Dextrocardia 55 1.508
665
ENC014 Enchondroma 28 1.500
666
ALP013 Alpha-Thalassemia Myelodysplasia Syndrome 30 1.490
667
SPP012 Suppressor of Tumorigenicity 11 19 1.472
668
OPT077 Optic Disc Pit 17 1.450
669
ERY010 Erythrasma 27 1.420
670
P XNT004 Xanthinuria 37 1.396
671
ADN020 Adenosarcoma 42 1.363
672
HYP765 Hyperbilirubinemia, Shunt, Primary 17 1.333
673
RMS001 Rem Sleep Behavior Disorder 47 1.333
674
BYS001 Byssinosis 28 1.288
675
SYN031 Synovial Chondromatosis 41 1.276
676
P SCL047 Sclerocornea 32 1.228
677
MND023 Mend Syndrome 49 1.212
678
EMY001 Eumycotic Mycetoma 34 1.194
679
LMR001 Lemierre's Syndrome 39 1.185
680
SPR018 Spermatocytoma 33 1.147
681
BRH001 Boerhaave Syndrome 16 1.055
682
LNG017 Lung Giant Cell Carcinoma 52 0.915
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