Search results for Glucose 6-phosphate

1500 hits were found for Glucose 6-phosphate

# Family MCID Name MIFTS Score
1
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 106.262
2
GLC003 Glucose Intolerance 53 70.684
3
c GLY060 Glycogen Storage Disease Ia 62 62.486
4
c GLY016 Glycogen Storage Disease Ib 41 60.107
5
GLC038 Glucose-6-Phosphate Translocase Deficiency 5 52.169
6
GLC081 Glucose Phosphate Isomerase Deficiency 19 48.612
7
HYP066 Hyperglycemia 60 48.101
8
HYP056 Hypoglycemia 65 43.518
9
c TYP009 Type 2 Diabetes Mellitus 91 41.300
10
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 40.572
11
P DBT009 Diabetes Mellitus 67 38.903
12
GLC008 Glucose Metabolism Disease 40 35.977
13
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 26 30.332
14
PRD004 Prediabetes Syndrome 52 29.769
15
c TYP008 Type 1 Diabetes Mellitus 77 29.280
16
HYP060 Hyperinsulinism 53 28.282
17
GLY111 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency Type Ib 36 27.918
18
GLC039 Glucosephosphate Isomerase Deficiency 17 27.362
19
GST033 Gestational Diabetes 60 26.192
20
c FST017 Fasting Plasma Glucose Level Quantitative Trait Locus 5 12 26.075
21
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 48 25.171
22
P HML002 Hemolytic Anemia 62 20.870
23
c MCR113 Microvascular Complications of Diabetes 3 52 18.537
24
c MCR133 Microvascular Complications of Diabetes 4 41 18.222
25
c MCR130 Microvascular Complications of Diabetes 6 41 18.222
26
c MCR120 Microvascular Complications of Diabetes 7 47 18.222
27
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 18.116
28
LPD008 Lipid Metabolism Disorder 61 17.489
29
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 17.462
30
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 17.460
31
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 17.460
32
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 17.460
33
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 17.460
34
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 17.460
35
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 17.460
36
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 17.460
37
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 17.460
38
P GLY013 Glycogen Storage Disease 59 16.899
39
NNL005 Non-Alcoholic Fatty Liver Disease 63 16.590
40
FTT001 Fatty Liver Disease 61 15.959
41
BLR008 Bilirubin Metabolic Disorder 57 15.748
42
NNT012 Neonatal Jaundice 53 14.921
43
P PLY011 Polycystic Ovary Syndrome 57 14.902
44
DFC004 Deficiency Anemia 74 14.409
45
c MCR115 Microvascular Complications of Diabetes 5 65 14.400
46
G6P001 G6pc3 Deficiency 23 13.716
47
DBT084 Diabetes Mellitus, Ketosis-Prone 59 13.668
48
MLR004 Malaria 77 13.578
49
HYP266 Hypoxia 56 13.359
50
48X005 48,xyyy 39 13.184
51
P KDN018 Kidney Disease 71 12.529
52
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 12.440
53
c HYP595 Hypertension, Essential 84 12.430
54
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 12.393
55
INS001 Insulinoma 59 12.371
56
P CRN300 Coronary Heart Disease 1 73 12.251
57
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 12.118
58
P HYP750 Hypertriglyceridemia, Familial 61 12.074
59
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 11.943
60
INS024 Insulin-Like Growth Factor I 77 11.880
61
CYS001 Cystic Fibrosis 77 11.639
62
c CHR684 Chronic Kidney Disease 73 11.526
63
P THL005 Thalassemia 56 11.460
64
P LVR013 Liver Disease 68 11.216
65
END086 End Stage Renal Disease 54 11.204
66
c HYP836 Hypercholesterolemia, Familial, 1 73 10.983
67
ACR007 Acromegaly 70 10.827
68
P VSC007 Vascular Disease 62 10.710
69
AGN016 Aging 53 10.629
70
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 10.573
71
ATH013 Atherosclerosis Susceptibility 63 10.510
72
ISC004 Ischemia 61 10.295
73
P MYC007 Myocardial Infarction 69 10.248
74
P HRT032 Heart Disease 84 10.145
75
LPP008 Lipoprotein Quantitative Trait Locus 65 10.101
76
c ACT075 Acute Myocardial Infarction 55 10.032
77
ART140 Arteries, Anomalies of 52 9.864
78
CRB039 Cerebrovascular Disease 65 9.805
79
RPD005 Rapidly Involuting Congenital Hemangioma 48 9.772
80
P ALZ034 Alzheimer Disease 87 9.467
81
STR067 Stroke, Ischemic 79 9.163
82
ANX004 Anoxia 40 8.986
83
P CTR002 Cataract 59 8.972
84
P HYP086 Hypothyroidism 68 8.920
85
CNG034 Congestive Heart Failure 69 8.843
86
P MTR004 Maturity-Onset Diabetes of the Young 66 8.767
87
P HYP076 Hyperthyroidism 53 8.737
88
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 8.691
89
P PNC044 Pancreatitis 61 8.661
90
P KRN004 Kernicterus 47 8.538
91
c ACT027 Acute Pancreatitis 60 8.485
92
CYT002 Cytokine Deficiency 43 8.301
93
LVR012 Liver Cirrhosis 62 8.299
94
P PNC035 Pancreatic Cancer 87 8.236
95
P SCK005 Sickle Cell Disease 56 8.152
96
P NRP001 Neuropathy 59 8.082
97
P HPT021 Hepatitis 68 8.063
98
PRT036 Peritonitis 65 8.046
99
c PRC016 Pre-Eclampsia 64 7.891
100
P NRB001 Neuroblastoma 66 7.863
101
RCK004 Rickets 64 7.805
102
DBT010 Diabetic Neuropathy 54 7.791
103
c ACT071 Acute Kidney Failure 60 7.728
104
LPT014 Leptin Deficiency or Dysfunction 77 7.708
105
NNL006 Non-Alcoholic Steatohepatitis 54 7.706
106
GLM045 Glioma 62 7.630
107
P MYP004 Myopathy 67 7.510
108
47X002 47,xyy 47 7.494
109
c VRL010 Viral Hepatitis 52 7.457
110
HYP014 Hyperuricemia 51 7.385
111
c HPT003 Hepatitis a 63 7.342
112
P BRS047 Breast Cancer 97 7.275
113
GLL048 Glial Tumor 51 7.263
114
URM002 Uremia 47 7.260
115
PRT037 Pertussis 49 7.247
116
CNG017 Congenital Nonspherocytic Hemolytic Anemia 34 7.243
117
CRB004 Cerebral Artery Occlusion 45 7.167
118
P ART022 Arthritis 70 7.098
119
HYP005 Hypokalemia 55 7.049
120
P SZR006 Seizure Disorder 69 6.996
121
CVD001 Covid-19 59 6.982
122
HLX001 Helix Syndrome 47 6.932
123
HYP043 Hyperandrogenism 47 6.921
124
P TRN020 Turner Syndrome 67 6.899
125
OCL069 Ocular Motor Apraxia 57 6.827
126
P SCH015 Schizophrenia 74 6.759
127
ALC007 Alcohol Dependence 65 6.729
128
P ENC018 Encephalopathy 62 6.639
129
HMG005 Hemoglobinopathy 55 6.631
130
P OVR082 Overgrowth Syndrome 41 6.609
131
P HPT023 Hepatocellular Carcinoma 95 6.591
132
c BTT014 Beta-Thalassemia 72 6.582
133
PRT251 Proteinuria, Chronic Benign 58 6.550
134
MTB004 Metabolic Acidosis 48 6.540
135
SCK003 Sickle Cell Anemia 74 6.518
136
P URN019 Urinary Tract Infection 48 6.482
137
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 6.481
138
PLS006 Plasmodium Vivax Malaria 51 6.442
139
IRN002 Iron Metabolism Disease 56 6.411
140
BRN071 Brain Injury 50 6.378
141
P RHM011 Rheumatoid Arthritis 81 6.370
142
CHL014 Cholera 62 6.304
143
P HYP050 Hyperinsulinemic Hypoglycemia 56 6.300
144
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 6.296
145
P NTR004 Neutropenia 62 6.287
146
P PLM037 Pulmonary Hypertension 69 6.264
147
P LNG032 Lung Cancer 98 6.258
148
BNR002 Bone Resorption Disease 47 6.226
149
c ATR087 Atrial Standstill 1 74 6.218
150
c ACT068 Acute Cystitis 60 6.199
151
P CLR023 Colorectal Cancer 100 6.196
152
P LCT001 Lactic Acidosis 50 6.189
153
BCT022 Bacterial Infectious Disease 55 6.157
154
GLB002 Glioblastoma 67 6.134
155
P MTH007 Methemoglobinemia 46 6.122
156
P PRP019 Peripheral Nervous System Disease 57 6.117
157
TRM010 Traumatic Brain Injury 50 6.071
158
FML035 Familial Hyperlipidemia 54 6.046
159
ATM095 Autoimmune Disease 61 6.039
160
ADN018 Adenoma 58 5.994
161
P PSR002 Psoriasis 63 5.981
162
P CRD246 Cardiovascular System Disease 55 5.916
163
P PRS040 Prostate Cancer 95 5.869
164
P RRH023 Rare Hereditary Hemochromatosis 52 5.865
165
PST011 Pustulosis of Palm and Sole 52 5.860
166
ALL029 Allergic Disease 61 5.855
167
P DRR001 Diarrhea 55 5.852
168
P PRD008 Periodontitis 63 5.822
169
FST010 Fasting Hypoglycemia 33 5.758
170
HMS001 Hemosiderosis 48 5.751
171
c SML038 Small Cell Cancer of the Lung 68 5.648
172
PLM129 Pulmonary Disease, Chronic Obstructive 74 5.630
173
P ALC033 Alcohol Use Disorder 67 5.559
174
RTN020 Retinal Vascular Disease 45 5.540
175
PRP027 Peripheral Vascular Disease 71 5.532
176
P MCR129 Microvascular Complications of Diabetes 1 67 5.495
177
SQM006 Squamous Cell Carcinoma 59 5.465
178
c HPT001 Hepatitis C 61 5.441
179
DWN001 Down Syndrome 70 5.439
180
PPL052 Papillomatosis, Confluent and Reticulated 34 5.436
181
MSC007 Muscle Hypertrophy 64 5.436
182
P GST053 Gastric Cancer 82 5.414
183
P PLY019 Polyneuropathy 52 5.400
184
MLD018 Mild Cognitive Impairment 48 5.384
185
c GLY017 Glycogen Storage Disease Ic 30 5.367
186
RNL077 Renal Fibrosis 46 5.357
187
P EPL164 Epilepsy 70 5.340
188
P ECL001 Eclampsia 52 5.290
189
P DMN002 Dementia 65 5.252
190
c HPT016 Hepatitis B 62 5.156
191
TYP007 Typhoid Fever 63 5.128
192
P CRD119 Cardiac Arrest 68 5.108
193
P INF032 Infertility 60 5.099
194
INT007 Intermediate Coronary Syndrome 53 5.081
195
GLB001 Gilbert Syndrome 53 5.046
196
P MYC084 Mycobacterium Tuberculosis 1 68 5.040
197
P ADN016 Adenocarcinoma 63 5.026
198
FNC009 Fanconi-Bickel Syndrome 53 5.013
199
ATS010 Autosomal Recessive Disease 42 5.006
200
RNL114 Renal Cell Carcinoma, Nonpapillary 79 4.979
201
P BCL017 B-Cell Lymphoma 57 4.970
202
P ART021 Arteriosclerosis 53 4.964
203
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 4.951
204
P MNN013 Meningitis 65 4.947
205
TXC005 Toxic Shock Syndrome 61 4.935
206
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.931
207
MNT002 Mental Depression 56 4.914
208
P MSC005 Muscular Dystrophy 66 4.886
209
TLN003 Telangiectasis 51 4.862
210
OST012 Osteoarthritis 77 4.833
211
GT001 Gout 63 4.805
212
P PRK039 Parkinsonism 55 4.803
213
c GLY008 Glycogen Storage Disease Ii 72 4.801
214
DPR016 Depression 64 4.794
215
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.784
216
P LNG064 Lung Cancer Susceptibility 3 69 4.760
217
c HMC039 Hemochromatosis, Type 1 73 4.756
218
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 4.754
220
PLS007 Plasmodium Falciparum Malaria 52 4.746
221
c GRV008 Graves Disease 1 54 4.737
222
HMN044 Human Immunodeficiency Virus Type 1 76 4.683
223
SVR004 Severe Combined Immunodeficiency 70 4.665
224
P LTR001 Lateral Sclerosis 57 4.612
225
P MSC003 Muscular Atrophy 52 4.609
226
HPT019 Hepatic Encephalopathy 59 4.604
227
FRC001 Fructose-1,6-Bisphosphatase Deficiency 50 4.595
228
P OVR042 Ovarian Cancer 88 4.594
229
DMP001 Dumping Syndrome 43 4.592
230
c AMY091 Amyotrophic Lateral Sclerosis 1 87 4.574
231
P MLT020 Multiple Sclerosis 79 4.566
232
LYS002 Lysosomal Storage Disease 51 4.565
233
P FBR017 Fibrosarcoma 55 4.559
234
P ATX030 Ataxia-Telangiectasia 80 4.546
235
END057 Endometrial Cancer 76 4.535
236
c MCR112 Microvascular Complications of Diabetes 2 42 4.529
237
GST045 Gastroenteritis 58 4.525
238
P PHC003 Pheochromocytoma 70 4.507
239
P LYM118 Lymphoma 66 4.507
240
P DDN001 Duodenal Ulcer 52 4.491
241
P CND004 Candidiasis 57 4.485
242
HMG002 Hemoglobinuria 50 4.476
243
PST092 Posttransplant Acute Limbic Encephalitis 29 4.470
244
c MCL062 Mucolipidosis Ii Alpha/beta 69 4.467
245
CHG001 Chagas Disease 65 4.466
246
P LKM062 Leukemia, Acute Lymphoblastic 69 4.423
247
CHL068 Cholestasis 61 4.417
248
CRH001 Crohn's Disease 80 4.414
249
P PNM007 Pneumonia 64 4.412
250
OST159 Osteogenic Sarcoma 66 4.407
251
ESP021 Esophageal Cancer 84 4.403
252
P HRP006 Herpes Simplex 65 4.399
253
LNG099 Lung Disease 62 4.398
254
c PLM164 Pulmonary Hypertension, Primary, 1 75 4.388
255
HPT004 Hepatic Coma 43 4.383
256
P HYP069 Hyperparathyroidism 62 4.382
257
c INH020 Inherited Metabolic Disorder 47 4.375
258
P LKM002 Leukemia 65 4.347
259
KRT002 Keratomalacia 54 4.346
260
OVR063 Overnutrition 42 4.335
261
DSS032 Disease by Infectious Agent 55 4.322
262
IMM167 Immune Deficiency Disease 76 4.300
263
DNT012 Dental Caries 53 4.279
264
GRW007 Growth Hormone Deficiency 47 4.278
265
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 4.266
266
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.262
267
IMP005 Impotence 52 4.254
268
P MJR001 Major Depressive Disorder 68 4.251
269
P HNT016 Huntington Disease 73 4.222
270
c DLT002 Dilated Cardiomyopathy 79 4.220
271
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 4.220
272
P CHR012 Chronic Granulomatous Disease 69 4.217
273
THY029 Thyroid Carcinoma 55 4.211
274
CRV035 Cervical Cancer 72 4.210
275
BRN004 Brain Edema 54 4.208
276
c CNG027 Congenital Hemolytic Anemia 49 4.191
277
c HPT073 Hepatitis C Virus 70 4.188
278
ADR040 Adrenal Gland Pheochromocytoma 45 4.149
279
HYP080 Hypogonadism 49 4.146
280
P MCR010 Microcephaly 59 4.107
281
P SRC025 Sarcoidosis 1 70 4.099
282
P MLN008 Melanoma 75 4.096
283
STM007 Stomatitis 52 4.086
284
CHR074 Choriocarcinoma 46 4.078
285
P GLM040 Glioma Susceptibility 1 70 4.062
286
P PRK057 Parkinson Disease, Late-Onset 79 4.062
287
P BPL003 Bipolar Disorder 56 4.033
288
SRC014 Sarcoma 64 3.990
289
P GLC113 Galactosemia I 65 3.976
290
CLN015 Colon Adenocarcinoma 64 3.973
291
P PLY018 Polycythemia 56 3.964
292
TRN015 Transient Cerebral Ischemia 62 3.950
293
MLG169 Malignant Astrocytoma 57 3.931
294
c ALP101 Alpha-Thalassemia 62 3.922
295
P RSP003 Respiratory Failure 73 3.920
296
P EXN002 Exanthem 58 3.914
297
CHL123 Chlamydia 58 3.912
298
ACQ007 Acquired Immunodeficiency Syndrome 58 3.905
299
MCL006 Macular Retinal Edema 56 3.901
300
c GLL024 Gallbladder Disease 1 53 3.898
301
MYL069 Myeloma, Multiple 76 3.853
302
P HRD011 Hereditary Spherocytosis 63 3.844
303
SLP001 Sleeping Sickness 56 3.837
304
P MYT002 Myotonic Dystrophy 51 3.834
305
P HYP083 Hypopituitarism 51 3.832
306
P LPR021 Leprosy 3 71 3.823
307
P ACN011 Acne 55 3.818
308
SPL018 Splenomegaly 47 3.813
309
PLM001 Pulmonary Tuberculosis 69 3.772
310
P ADL010 Adult Respiratory Distress Syndrome 70 3.772
311
P PRP029 Porphyria 60 3.765
312
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.761
313
HRW001 Hair Whorl 35 3.753
314
HYP026 Hypoglycemic Coma 37 3.739
315
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 3.720
316
ATN005 Autonomic Dysfunction 45 3.715
317
PLY150 Polykaryocytosis Inducer 29 3.711
318
c MJR022 Major Affective Disorder 8 37 3.701
319
c MJR024 Major Affective Disorder 9 40 3.701
320
PLY105 Polycystic Ovary Syndrome 1 39 3.668
321
DBT007 Diabetic Cataract 36 3.665
322
P TRM003 Tremor 50 3.641
323
HNS001 Hansen's Disease 32 3.640
324
c BCT007 Bacterial Meningitis 55 3.635
325
BRN028 Brain Cancer 73 3.631
326
P KLZ004 Kala-Azar 1 41 3.617
327
LSH001 Leishmaniasis 63 3.617
328
P DYS154 Dystonia 64 3.615
329
NRL016 Neural Tube Defects 80 3.603
330
CRT065 Cortisone Reductase Deficiency 1 25 3.596
331
c BRN108 Branchiootic Syndrome 1 63 3.578
332
CLT003 Colitis 63 3.575
333
P MVM001 Movement Disease 61 3.568
334
VSC002 Vascular Dementia 59 3.559
335
P GLM007 Glomerulonephritis 59 3.547
336
CRB037 Cerebral Palsy 66 3.531
337
c CNG411 Congenital Disorder of Glycosylation, Type in 66 3.531
338
c SYS001 Systemic Lupus Erythematosus 85 3.516
339
P RHB003 Rhabdomyosarcoma 66 3.509
340
P KDN017 Kidney Cancer 60 3.506
341
DBT008 Diabetic Angiopathy 47 3.503
342
P GRV001 Graves' Disease 54 3.491
343
PTT037 Pituitary Tumors 44 3.490
344
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 3.466
345
IRN001 Iron Deficiency Anemia 58 3.463
346
ULC004 Ulcerative Colitis 74 3.462
347
PRN019 Perinatal Necrotizing Enterocolitis 60 3.455
348
NRR001 Neuroretinitis 42 3.453
349
DRM006 Dermatitis 61 3.447
350
MNG006 Monogenic Diabetes 45 3.443
351
P BRS044 Breast Adenocarcinoma 58 3.423
352
P THY032 Thyroiditis 56 3.423
353
c LKM063 Leukemia, Chronic Myeloid 70 3.421
354
SPN035 Spindle Cell Sarcoma 51 3.417
355
P LPS004 Lupus Erythematosus 61 3.411
356
P ATT013 Attention Deficit-Hyperactivity Disorder 65 3.376
357
SCH012 Schizoaffective Disorder 49 3.365
358
P MCL001 Mucolipidosis 49 3.354
359
SNL007 Senile Cataract 40 3.339
360
P ENC004 Encephalitis 61 3.329
361
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 3.326
362
HYP020 Hyperprolactinemia 63 3.322
363
P MYL006 Myeloid Leukemia 60 3.310
364
CRB090 Cerebral Hypoxia 42 3.292
365
SCH014 Schistosomiasis 56 3.289
366
c PRM005 Primary Hyperparathyroidism 59 3.285
367
CRN030 Coronary Stenosis 50 3.275
368
THR024 Thrombosis 56 3.273
369
HMP009 Haemophilus Influenzae 41 3.264
370
P TMP001 Temporal Lobe Epilepsy 49 3.254
371
CHL065 Cholangiocarcinoma 57 3.249
372
c HMG003 Hemoglobin E Disease 41 3.248
373
c HPT007 Hepatitis E 50 3.220
374
P LCH002 Lichen Planus 54 3.218
375
P SPP010 Suppressor of Tumorigenicity 3 50 3.217
376
P BLD134 Bladder Cancer 79 3.206
377
SVR001 Severe Acute Respiratory Syndrome 68 3.202
378
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 3.201
379
P BRB001 Beriberi 44 3.197
380
ENT011 Enterocolitis 55 3.190
381
P BND020 Bone Disease 60 3.178
382
c HNT004 Huntington Disease-Like 2 51 3.159
383
URT049 Urate Oxidase, Pseudogene 24 3.154
384
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 3.152
385
SYN007 Synovitis 54 3.144
386
ISL001 Islet Cell Tumor 55 3.144
387
P ALP008 Alopecia 53 3.143
388
c CNG006 Congenital Hypothyroidism 63 3.132
389
c ACT134 Acute Liver Failure 57 3.122
390
RTN023 Retinitis 45 3.121
391
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 3.120
392
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 3.120
393
HYP017 Hypophosphatemia 49 3.108
394
P MLN007 Male Infertility 56 3.099
395
P HYD006 Hydrocephalus 62 3.090
396
P AMY004 Amyloidosis 69 3.089
397
P HYP730 Hypogonadotropic Hypogonadism 57 3.086
398
c PCH010 Pachyonychia Congenita 3 43 3.080
399
CHL004 Cholelithiasis 48 3.066
400
c MGR028 Migraine with or Without Aura 1 63 3.053
401
CRD137 Cardiogenic Shock 56 3.034
402
DWR001 Dwarfism 44 3.007
403
c SVR003 Severe Congenital Neutropenia 59 2.997
404
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.989
405
PSY004 Psychotic Disorder 66 2.987
406
CYN002 Cyanosis, Transient Neonatal 43 2.987
407
STT001 Status Epilepticus 58 2.983
408
HGH043 High Grade Glioma 46 2.981
409
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.977
410
PLC005 Placental Insufficiency 55 2.975
411
AMN001 Amenorrhea 53 2.974
412
P HRD012 Hereditary Elliptocytosis 55 2.969
413
P NSP012 Nasopharyngeal Carcinoma 60 2.966
414
SPN051 Spondylitis 51 2.959
415
P RTN022 Retinal Vein Occlusion 54 2.955
416
DSS008 Disease of Mental Health 74 2.949
417
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 2.931
418
INT079 Intrahepatic Cholangiocarcinoma 51 2.916
419
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.907
420
ANR040 Aneurysm 60 2.906
421
TRY001 Trypanosomiasis 50 2.901
422
P GND004 Gonadal Dysgenesis 46 2.899
423
MST005 Mastitis 52 2.892
424
RST023 Resting Heart Rate, Variation in 40 2.882
425
P HYP061 Hypertrophic Cardiomyopathy 68 2.873
426
FRC013 Fructose Utilization 15 2.870
427
PNC129 Pancreatic Adenocarcinoma 64 2.863
428
ORL011 Oral Cancer 60 2.860
429
PLM010 Pulmonary Edema 54 2.852
430
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.844
431
P RTN018 Retinal Disease 53 2.842
432
WRN001 Werner Syndrome 69 2.841
433
P FNC004 Fanconi Syndrome 60 2.837
434
DFF005 Diffuse Large B-Cell Lymphoma 55 2.831
435
VRL011 Viral Infectious Disease 60 2.829
436
PLC002 Plica Syndrome 35 2.813
437
PRP007 Priapism 46 2.810
438
STN013 Stenotrophomonas Maltophilia Infection 26 2.803
439
P VSC011 Vasculitis 61 2.799
440
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 2.797
441
CHR073 Choreatic Disease 53 2.797
442
P RTN024 Retinoblastoma 72 2.786
443
PRS045 Prostatic Hypertrophy 53 2.773
444
P PLM036 Pulmonary Fibrosis 65 2.771
445
SBC016 Subacute Delirium 42 2.767
446
MSC157 Muscular Dystrophy, Duchenne Type 78 2.766
447
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.759
448
P GCH001 Gaucher's Disease 69 2.755
449
DYS015 Dysentery 49 2.749
450
P TXP001 Toxoplasmosis 59 2.746
451
BRC012 Brucellosis 66 2.735
452
P SYP003 Syphilis 59 2.728
453
PRS021 Prostatic Adenoma 43 2.720
454
PHN003 Phenylketonuria 76 2.718
455
CNT047 Contact Dermatitis 56 2.713
456
ACT098 Acute Erythroid Leukemia 55 2.708
457
CHC001 Chickenpox 56 2.705
458
P DBT005 Diabetes Insipidus 54 2.701
459
GTR002 Goiter 52 2.688
460
CRT020 Cortisone Reductase Deficiency 36 2.686
461
THY030 Thyroid Gland Disease 50 2.684
462
P THR014 Thrombocytopenia 66 2.681
463
ACT003 Acute Kidney Tubular Necrosis 46 2.680
464
PRT058 Pure Autonomic Failure 58 2.679
465
PRS129 Prostatic Hyperplasia, Benign 48 2.675
466
P CLC063 Celiac Disease 1 65 2.669
467
PRP016 Paraplegia 52 2.660
468
PST028 Post-Traumatic Stress Disorder 58 2.659
469
GNG013 Gingivitis 59 2.644
470
HMN047 Human Cytomegalovirus Infection 59 2.643
471
NPH009 Nephrolithiasis 54 2.639
472
P MYC008 Myocarditis 59 2.635
473
SNS003 Sensory Peripheral Neuropathy 51 2.629
474
INF009 Inflammatory Spondylopathy 30 2.627
475
MYL009 Myelodysplastic Syndrome 67 2.620
476
PLR007 Pleural Empyema 50 2.612
477
P NRF002 Neurofibromatosis 60 2.603
478
PRT038 Protein-Energy Malnutrition 53 2.601
479
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 2.596
480
ORL015 Oral Squamous Cell Carcinoma 43 2.595
481
c LKM061 Leukemia, Acute Myeloid 83 2.591
482
BTT017 Beta-Thalassemia Major 54 2.586
483
SPS057 Spasticity 43 2.569
484
CNN005 Connective Tissue Disease 66 2.566
485
c TBR025 Tuberous Sclerosis 1 84 2.564
486
GNT167 Genetic Obesity 33 2.557
487
GLM044 Glomerular Disease 34 2.549
488
HMC014 Homocysteinemia 52 2.548
489
LYM019 Lymphosarcoma 46 2.543
490
P EYD002 Eye Disease 57 2.542
491
c ANM038 Anemia, Autoimmune Hemolytic 63 2.541
492
ART016 Aortic Aneurysm 68 2.540
493
MNN043 Meningioma, Familial 79 2.539
494
SYN036 Syncope 44 2.533
495
VLV047 Volvulus of Midgut 55 2.525
496
P MYG005 Myoglobinuria 40 2.525
497
HYD038 Hydrops Fetalis, Nonimmune 57 2.522
498
c LYM150 Lymphatic Malformation 7 43 2.522
499
FLR002 Filariasis 55 2.516
500
OST017 Osteomyelitis 63 2.512
501
P MTR014 Motor Neuron Disease 65 2.508
502
c ELL006 Elliptocytosis 3 34 2.505
503
c ELL005 Elliptocytosis 2 36 2.505
504
P ACT241 Acute Bilirubin Encephalopathy 26 2.504
505
LYM027 Lymphopenia 56 2.500
506
CLR030 Clear Cell Renal Cell Carcinoma 53 2.497
507
P ASP006 Aspergillosis 71 2.487
508
PPT005 Peptic Ulcer Disease 58 2.482
509
P NPH012 Nephrotic Syndrome 61 2.482
510
P DRM053 Dermatitis, Atopic 65 2.480
511
TTN003 Tetanus 64 2.479
512
P HML001 Hemolytic-Uremic Syndrome 52 2.471
513
ALL010 Allergic Contact Dermatitis 55 2.467
514
c JVN010 Juvenile Rheumatoid Arthritis 52 2.467
515
c THY107 Thymoma, Familial 42 2.467
516
P THY023 Thymoma 64 2.467
517
KWS001 Kwashiorkor 44 2.464
518
CHL147 Chlamydia Pneumonia 47 2.462
519
c SVR005 Severe Pre-Eclampsia 49 2.461
520
PLM033 Pulmonary Embolism 58 2.456
521
SKN016 Skin Disease 63 2.453
522
P HRD144 Hereditary Mixed Polyposis Syndrome 54 2.453
524
P RNL007 Renal Tubular Acidosis 52 2.441
525
ALL014 Allergic Encephalomyelitis 34 2.441
526
c SPN225 Spondyloarthropathy 1 70 2.438
527
LYM002 Lymphoplasmacyte-Rich Meningioma 35 2.433
528
SCR001 Secretory Meningioma 40 2.433
529
INT395 Intracranial Meningioma 47 2.433
530
P OBS001 Obstructive Jaundice 49 2.425
531
c GLY003 Glycogen Storage Disease Iii 60 2.425
532
P MTC069 Mitochondrial Disorders 57 2.423
533
CHY002 Chylomicron Retention Disease 64 2.415
534
P INS002 in Situ Carcinoma 52 2.405
535
XLN228 X-Linked Recessive Disease 24 2.402
536
c RRC031 Rare Constitutional Hemolytic Anemia Due to an Enzyme Disorder 5 2.392
537
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.391
538
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.391
539
c FML021 Familial Hypercholesterolemia 71 2.390
540
c HNT011 Huntington Disease-Like 3 33 2.389
541
FBR012 Fabry Disease 71 2.384
542
SPT005 Spotted Fever 49 2.383
543
LYM143 Lymphoma, Non-Hodgkin, Familial 74 2.380
544
P INF037 Inflammatory Bowel Disease 53 2.376
545
P UVT001 Uveitis 57 2.352
546
PLS011 Plasmacytoma 56 2.344
547
P TBR001 Tuberous Sclerosis 69 2.334
548
LMB062 Limb Ischemia 55 2.332
549
PNC034 Pancreas Disease 49 2.331
550
GST019 Gastrointestinal Stromal Tumor 78 2.325
551
CRT015 Carotid Artery Occlusion 45 2.318
552
P CNJ013 Conjunctivitis 66 2.313
553
ARG004 Argyria 26 2.312
554
P CHN012 Chondrosarcoma 56 2.307
555
MYL005 Myelofibrosis 70 2.306
556
MDD011 Mood Disorder 61 2.304
557
P OPT006 Optic Nerve Disease 57 2.302
558
P MLG056 Malignant Hyperthermia 65 2.290
559
ANX010 Anxiety 70 2.274
560
GST023 Gastric Ulcer 52 2.267
561
MCR141 Mucormycosis 59 2.263
562
P INF038 Influenza 68 2.261
563
P RTN008 Retinitis Pigmentosa 79 2.260
564
c EXD008 Exudative Vitreoretinopathy 1 71 2.258
565
P NJM001 Nijmegen Breakage Syndrome 75 2.257
566
P HYP265 Hypotonia 42 2.254
567
SVN002 Sveinsson Chorioretinal Atrophy 45 2.252
568
CHR178 Chromosomal Triplication 33 2.246
569
P OVR049 Ovarian Disease 50 2.246
570
VCC001 Vaccinia 49 2.240
571
P END033 Endocarditis 58 2.234
572
CTN007 Cutaneous Leishmaniasis 61 2.226
573
INT323 Intraocular Pressure Quantitative Trait Locus 63 2.219
574
PRT013 Portal Hypertension 59 2.219
575
P CLR019 Color Blindness 47 2.219
576
P LKM071 Leukemia, Chronic Lymphocytic 74 2.212
577
P SJG008 Sjogren Syndrome 60 2.209
578
LRN003 Learning Disability 49 2.208
579
BCT004 Bacteriuria 48 2.205
580
P PYL005 Pyelonephritis 56 2.203
581
PLG002 Plague 58 2.194
582
CRY005 Cryptococcosis 61 2.192
583
PSR001 Psoriatic Arthritis 61 2.191
584
FNG017 Fungal Infectious Disease 54 2.188
585
c GLC079 Glaucoma 1, Open Angle, P 23 2.179
586
P SPN046 Spinal Muscular Atrophy 62 2.176
587
c ACT004 Acute Diarrhea 40 2.174
588
P LCT002 Lactose Intolerance 51 2.170
589
LPT001 Leptospirosis 65 2.169
590
VTM002 Vitamin B12 Deficiency 48 2.169
591
P TMP003 Temporal Arteritis 68 2.168
592
BRS051 Breast Disease 58 2.163
593
DNG002 Dengue Hemorrhagic Fever 59 2.161
594
PRC002 Paracoccidioidomycosis 53 2.157
595
HPT022 Hepatoblastoma 54 2.147
596
P PLY041 Polymyositis 58 2.147
597
DPH001 Diphtheria 59 2.141
598
THL010 Thalassemia Minor 30 2.139
599
VTM033 Vitamin K Deficiency Bleeding 49 2.136
600
P RHN004 Rhinitis 56 2.127
601
CHL067 Cholecystitis 59 2.124
602
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 2.123
603
CLR033 Color Vision Deficiency 41 2.117
604
WLS001 Wilson Disease 70 2.112
605
HRY003 Hairy Cell Leukemia 53 2.110
606
RBF001 Riboflavin Deficiency 49 2.109
607
BRN056 Bronchopulmonary Dysplasia 57 2.108
608
PRC013 Pericarditis 53 2.100
609
CRD132 Cardiac Conduction Defect 59 2.094
610
HLC007 Helicobacter Pylori Infection 67 2.090
611
CRV002 Cervix Uteri Carcinoma in Situ 48 2.089
612
CRV045 Cervical Intraepithelial Neoplasia 38 2.089
613
c PRG106 Progressive Muscular Dystrophy 31 2.081
614
BLD052 Blood Group Incompatibility 31 2.079
615
SFT003 Soft Tissue Sarcoma 43 2.079
616
DMN031 Dementia, Lewy Body 65 2.077
617
P APL001 Aplastic Anemia 72 2.071
619
SQM013 Squamous Cell Carcinoma, Head and Neck 75 2.059
620
P MYC033 Myoclonus 46 2.056
621
MNN009 Meningoencephalitis 47 2.055
622
P SDR002 Siderosis 42 2.054
623
NRT001 Neurotic Disorder 56 2.053
624
P AST005 Asthma 75 2.051
625
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.049
626
P SYS005 Systemic Scleroderma 73 2.046
627
PNC001 Pancytopenia 52 2.044
628
P ANP001 Anaplastic Large Cell Lymphoma 59 2.041
629
ART004 Aortic Atherosclerosis 46 2.038
630
ENT004 Enthesopathy 51 2.035
631
MYC079 Myoclonic Epilepsy of Lafora 63 2.024
632
CNT016 Central Retinal Vein Occlusion 53 2.021
633
THR004 Thrombocytosis 52 2.016
634
P RTN016 Retinal Degeneration 52 2.016
635
c SCL052 Scleroderma, Familial Progressive 60 2.010
636
FRN006 Frontotemporal Dementia 68 2.006
637
NRM005 Neuromuscular Disease 62 2.004
638
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.998
639
c LKM005 Leukemia, T-Cell, Chronic 33 1.998
640
BRS099 Breast Ductal Carcinoma 61 1.987
641
NRN005 Neuronal Ceroid-Lipofuscinoses 61 1.986
642
c PRG020 Paragangliomas 3 39 1.983
643
P MTC133 Mitochondrial Myopathy 51 1.977
644
BRK010 Burkitt Lymphoma 65 1.972
645
HPT067 Hepatocellular Adenoma 42 1.971
646
PYR009 Pyridoxine Deficiency Anemia 35 1.971
647
P WSK001 Wiskott-Aldrich Syndrome 72 1.969
648
MLD001 Melioidosis 67 1.968
649
P HMC002 Homocystinuria 52 1.966
650
MTH071 Methane Production 24 1.965
651
BLC004 Blackwater Fever 26 1.960
652
P SKN015 Skin Carcinoma 71 1.960
653
P FRG001 Fragile X Syndrome 70 1.957
654
ALL006 Allergic Asthma 55 1.954
655
MRS001 Marasmus 41 1.952
656
PLY001 Polycythemia Vera 69 1.949
657
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.947
658
OVR094 Ovarian Epithelial Cancer 39 1.943
659
P HMP007 Hemophilia 52 1.943
660
DST006 Diastolic Heart Failure 45 1.934
661
ASP004 Asphyxia Neonatorum 50 1.932
662
ALD013 Aldosterone-Producing Adenoma 36 1.930
663
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 1.928
664
CRC021 Carcinosarcoma 62 1.923
665
QDR001 Quadriplegia 49 1.912
666
P DNG005 Dengue Virus 55 1.911
667
P SLM003 Salmonellosis 54 1.906
668
GRN017 Granulocytopenia 42 1.904
669
CCC002 Coccidiosis 50 1.903
670
BCK006 Back Pain 43 1.902
671
c THR092 Thrombophilia Due to Thrombin Defect 74 1.894
672
KDN013 Kidney Hypertrophy 33 1.889
673
P LKD001 Leukodystrophy 58 1.885
674
c ANM036 Anemia, Sideroblastic, 1 56 1.880
675
INT066 Interstitial Lung Disease 60 1.877
676
DSS009 Disseminated Intravascular Coagulation 56 1.876
677
P BRS053 Breast Fibroadenoma 48 1.872
678
HYP141 Hyperphenylalaninemia 42 1.871
679
PCK003 Pick Disease of Brain 70 1.865
680
RHM001 Rheumatic Fever 59 1.862
681
VLK001 Volkmann Contracture 23 1.859
682
KPS004 Kaposi Sarcoma 76 1.857
683
ASP003 Aseptic Meningitis 50 1.854
684
BTN002 Boutonneuse Fever 42 1.849
685
HYP025 Hyperphosphatemia 47 1.848
686
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.847
687
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.839
688
P NRN021 Neuronal Ceroid Lipofuscinosis 64 1.837
689
PLM031 Poliomyelitis 62 1.834
690
P RNL015 Renal Hypertension 45 1.833
691
PRM329 Premature Aging 36 1.831
692
c ACT073 Acute Leukemia 59 1.824
693
HRT011 Heart Septal Defect 49 1.823
694
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.802
695
P NMN002 Niemann-Pick Disease 60 1.802
696
P PSD015 Pseudohypoparathyroidism 54 1.801
697
KWS002 Kawasaki Disease 65 1.799
698
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.794
699
SDD001 Sudden Infant Death Syndrome 60 1.793
700
ACT209 Acatalasemia 44 1.792
701
LYM040 Lymphoblastic Lymphoma 53 1.789
702
VSC003 Visceral Leishmaniasis 54 1.784
703
P DRM010 Dermatomyositis 61 1.784
704
DCT002 Ductal Carcinoma in Situ 58 1.780
705
P SNS001 Sensorineural Hearing Loss 60 1.774
706
ERL001 Early Myoclonic Encephalopathy 62 1.772
707
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.772
708
CHD001 Chediak-Higashi Syndrome 66 1.771
709
URL001 Urolithiasis 45 1.770
710
ALC006 Alcoholic Hepatitis 61 1.766
711
TRN018 Transitional Cell Carcinoma 56 1.764
712
MCR018 Microcytic Anemia 46 1.764
713
c INF071 Inflammatory Bowel Disease 1 65 1.764
714
FLR001 Filarial Elephantiasis 59 1.762
715
HST010 Histiocytosis 49 1.762
716
6PH001 6-Phosphogluconate Dehydrogenase Deficiency 20 1.754
717
PHS025 Phosphatase, Acid, of Tissues 28 1.753
718
TRT001 Teratocarcinoma 41 1.743
719
BBS001 Babesiosis 48 1.737
720
P MDL005 Medulloblastoma 75 1.736
721
CHL039 Choledocholithiasis 37 1.731
722
MTC206 Mitochondrial Complex Iv Deficiency, Nuclear Type 5 52 1.729
723
NPH003 Nephrocalcinosis 49 1.728
724
P CHR071 Charcot-Marie-Tooth Disease 64 1.728
725
CLR109 Colorectal Adenocarcinoma 50 1.725
726
LWG006 Low Grade Glioma 41 1.724
727
TRC022 Tricuspid Valve Insufficiency 46 1.724
728
P GRF003 Graft-Versus-Host Disease 71 1.718
729
LWC002 Lowe Oculocerebrorenal Syndrome 68 1.717
730
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.708
731
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 1.708
732
BTN004 Biotin Deficiency 44 1.702
733
STT041 Stuttering 52 1.698
734
SMN007 Seminoma 42 1.697
735
FCT001 Factor Viii Deficiency 61 1.694
736
c HMP029 Hemophilia a 69 1.694
737
SYS071 Systemic Autoimmune Disease 35 1.693
738
INF034 Infective Endocarditis 53 1.692
739
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.690
740
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.678
741
P LMY004 Leiomyosarcoma 62 1.678
742
P SML001 Small Cell Carcinoma 52 1.673
743
CHL013 Cholecystolithiasis 37 1.669
744
TTH006 Tooth Disease 51 1.669
745
RTN017 Retinal Detachment 60 1.656
746
HSH003 Hashimoto Thyroiditis 60 1.653
747
c PNC106 Pancreatic Agenesis 1 51 1.646
748
P MYS003 Myasthenia Gravis 67 1.635
749
c SPR086 Spermatogenic Failure 3 47 1.634
750
P CRP001 Carpal Tunnel Syndrome 65 1.633
751
THY122 Thyroid Gland Cancer 59 1.632
752
AMN006 Aminoaciduria 37 1.631
753
P HMG032 Hemoglobin H Disease 51 1.625
754
MTR002 Mitral Valve Insufficiency 51 1.625
755
FRC011 Fructose Intolerance, Hereditary 55 1.623
756
MLG086 Malignant Hyperthermia Susceptibility 40 1.623
757
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.622
758
MYX004 Myxedema 43 1.617
759
P ATS364 Autism 72 1.613
760
TNS005 Tonsillitis 57 1.611
761
MTC005 Mitochondrial Metabolism Disease 44 1.610
762
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.607
763
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 1.606
764
c NMN015 Niemann-Pick Disease, Type C1 68 1.603
765
LWF001 Low-Flow Priapism 16 1.602
766
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 36 1.601
767
ALL003 Allergic Rhinitis 66 1.583
768
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.580
769
c HMG004 Hemoglobin D Disease 34 1.576
770
NRM001 Neuromyelitis Optica 60 1.576
771
TRD006 Tardive Dyskinesia 53 1.575
772
c GCH015 Gaucher Disease, Type I 67 1.575
773
LST001 Listeriosis 59 1.574
774
P FML187 Familial Hypertension 34 1.570
775
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 1.568
776
PCD001 Pica Disease 38 1.564
777
OVL001 Ovalocytosis, Southeast Asian 34 1.558
778
P OPN001 Open-Angle Glaucoma 55 1.551
779
P HYP024 Hypoparathyroidism 55 1.547
780
RCK002 Rocky Mountain Spotted Fever 34 1.545
781
P CHL066 Cholangitis 51 1.542
782
P MNC007 Monocytic Leukemia 48 1.532
783
P FRD001 Friedreich Ataxia 62 1.531
784
GST092 Gastroesophageal Reflux 59 1.528
785
P GST044 Gastritis 55 1.523
786
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.515
787
c MJR008 Major Affective Disorder 2 34 1.514
788
ADL030 Adult-Onset Still's Disease 59 1.514
789
PPL022 Papilloma 53 1.513
790
PTH003 Pathologic Nystagmus 52 1.512
791
RTN003 Retinal Ischemia 48 1.511
792
P FTL001 Fetal Alcohol Syndrome 55 1.510
793
c ATS007 Autism Spectrum Disorder 71 1.503
794
SPN119 Spondylarthropathy 37 1.502
795
PRN011 Pernicious Anemia 52 1.490
796
MYL031 Myeloproliferative Neoplasm 66 1.488
797
XRD010 Xeroderma Pigmentosum, Variant Type 72 1.486
798
SQM002 Squamous Cell Papilloma 45 1.485
799
OCL006 Ocular Hypertension 53 1.485
800
BLS002 Blastomycosis 47 1.483
801
P LRY044 Larynx Cancer 53 1.482
802
P HYP098 Hypereosinophilic Syndrome 66 1.478
803
P CRG003 Crigler-Najjar Syndrome, Type I 64 1.473
804
ADG002 Audiogenic Seizures 25 1.466
805
P SPN052 Spondyloarthropathy 54 1.465
806
MTH009 Mouth Disease 57 1.464
807
CRG004 Crigler-Najjar Syndrome, Type Ii 46 1.455
808
P SDR003 Sideroblastic Anemia 49 1.455
809
FLL031 Follicular Adenoma 40 1.450
810
HYP063 Hypersplenism 51 1.450
811
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 1.445
812
LNG031 Lung Benign Neoplasm 51 1.444
813
c NMN014 Niemann-Pick Disease, Type C2 49 1.444
814
BCT021 Bacterial Sepsis 43 1.443
815
ERY003 Erythema Multiforme 56 1.439
816
P ADL017 Adult T-Cell Leukemia 53 1.438
817
P LNG028 Long Qt Syndrome 63 1.436
818
RFR010 Refractory Anemia 49 1.433
819
MRK001 Merkel Cell Carcinoma 64 1.426
820
SVR097 Severe Cutaneous Adverse Reaction 68 1.425
821
ERY066 Erythema Multiforme Major 29 1.425
822
PRT002 Paratyphoid Fever 54 1.424
823
BNS003 Binswanger's Disease 41 1.424
824
END041 Endometrial Adenocarcinoma 63 1.418
825
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.418
826
AST054 Australia Antigen 25 1.415
827
P MTC003 Metachromatic Leukodystrophy 71 1.412
828
FML063 Familial Glucocorticoid Deficiency 58 1.411
829
DYS073 Dysphagia 53 1.409
830
THY006 Thymus Lymphoma 27 1.408
831
EXP004 Exophthalmos 50 1.407
832
BRT043 Bartonellosis 35 1.402
833
P TRT010 Teratoma 50 1.402
834
TST015 Testicular Disease 42 1.401
835
KRT008 Keratopathy 46 1.400
836
HRN029 Hearing Loss, Noise-Induced 37 1.396
837
ADR016 Adrenal Cortical Carcinoma 61 1.396
839
THY125 Thyroid Gland Medullary Carcinoma 48 1.392
840
ABT001 Abetalipoproteinemia 68 1.385
841
OTT002 Otitis Media 70 1.384
842
ALC010 Alcoholic Cardiomyopathy 42 1.381
843
P FML018 Familial Mediterranean Fever 73 1.378
844
P NRV007 Nervous System Disease 65 1.377
845
c FTL070 Fetal Akinesia Deformation Sequence 2 36 1.376
846
GST040 Gastric Adenocarcinoma 66 1.369
847
P CYS018 Cystitis 58 1.368
848
c FNC027 Fanconi Anemia, Complementation Group a 80 1.364
849
SCB001 Scabies 49 1.361
850
P HML033 Hemolytic Uremic Syndrome, Atypical 1 67 1.360
851
c DMN023 Diamond-Blackfan Anemia 1 68 1.360
852
ONC002 Onchocerciasis 50 1.359
853
ILS001 Ileus 49 1.354
854
ALB002 Albinism 46 1.350
855
ORL005 Oral Candidiasis 55 1.349
856
ANP005 Anaplastic Astrocytoma 59 1.348
857
NNT011 Neonatal Anemia 34 1.347
858
TNG007 Tongue Carcinoma 55 1.345
859
LPR001 Lepromatous Leprosy 49 1.341
860
ADR048 Adrenal Hyperplasia, Congenital, Due to 3-Beta-Hydroxysteroid Dehydrogenase 2 Deficiency 34 1.330
861
P LPM005 Lipomatosis 47 1.323
862
TRC008 Trachoma 53 1.318
863
c MCP001 Mucopolysaccharidosis Iii 69 1.317
864
IRD001 Iridocyclitis 54 1.315
865
MNG007 Manganese Poisoning 28 1.313
866
PPL002 Papillary Carcinoma 46 1.312
867
INT067 Interstitial Nephritis 46 1.303
868
P RNV001 Renovascular Hypertension 48 1.294
869
ORN001 Ornithosis 39 1.293
870
SPL009 Splenic Sequestration 35 1.292
871
c SVR110 Severe Congenital Neutropenia 4 16 1.290
872
CHR682 Chronic Bilirubin Encephalopathy 37 1.284
873
c HRD010 Hereditary Spastic Paraplegia 65 1.283
874
c GLY007 Glycogen Storage Disease Iv 58 1.283
875
P CRC039 Coarctation of Aorta 46 1.282
876
CRT072 Creutzfeldt-Jakob Disease 67 1.272
877
HVY002 Heavy Metal Poisoning 22 1.271
878
BRN014 Bronchopneumonia 52 1.268
879
HST011 Histoplasmosis 54 1.267
880
P CCK001 Cockayne Syndrome 67 1.267
881
FCL012 Facial Paralysis 49 1.263
882
c ATM011 Autoimmune Hepatitis 62 1.258
883
CRV040 Cervix Carcinoma 50 1.252
884
QFV001 Q Fever 61 1.250
885
CHR619 Chromosome 2q35 Duplication Syndrome 64 1.250
886
c WLM013 Wilms Tumor 1 65 1.250
887
c GLY011 Glycogen Storage Disease Vii 54 1.249
888
HMF011 Hemifacial Spasm, Familial 33 1.239
889
P HMF004 Hemifacial Spasm 38 1.239
890
P VNT002 Ventricular Septal Defect 58 1.239
891
CLR132 Colorblindness, Partial, Deutan Series 31 1.237
892
BRN024 Bronchitis 67 1.233
893
c CHR098 Chronic Pyelonephritis 34 1.228
894
HYP029 Hyperthyroxinemia 32 1.227
895
CPR004 Coproporphyria, Hereditary 57 1.224
896
SCR011 Scrapie 39 1.223
897
P MJR007 Major Affective Disorder 1 42 1.222
898
END062 Endometrial Hyperplasia 47 1.219
899
CLN003 Clonorchiasis 42 1.218
900
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 25 1.214
901
DRM014 Dermatofibrosarcoma Protuberans 64 1.213
902
LKC009 Leukocyte Adhesion Deficiency, Type I 69 1.208
903
CMB007 Combined Immunodeficiency 56 1.205
904
RHM028 Rheumatic Heart Disease 55 1.202
905
c LKM070 Leukemia, Acute Monocytic 56 1.201
906
P MTR003 Mitral Valve Stenosis 53 1.201
907
CRY003 Cryptosporidiosis 55 1.197
908
c CNG223 Congenital Methemoglobinemia 39 1.196
909
ACT017 Acute Chest Syndrome 50 1.196
910
CYS010 Cystinosis 61 1.189
911
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 1.186
912
RYS001 Reye Syndrome 49 1.183
913
DNG003 Dengue Disease 65 1.181
914
P CMP008 Compartment Syndrome 49 1.180
915
P PTS002 Ptosis 52 1.177
916
GLT007 Glutathione Synthetase Deficiency 48 1.170
917
LYS029 Lysosomal Disease 30 1.169
918
PHS018 Phosphorylase Kinase Deficiency 37 1.168
919
c ERY067 Erythrocytosis, Familial, 8 34 1.167
921
OLV001 Olivopontocerebellar Atrophy 50 1.162
922
PNM001 Pneumocystosis 60 1.153
923
KLB003 Klebsiella Pneumonia 49 1.153
924
LSC001 Lesch-Nyhan Syndrome 62 1.152
925
HYP001 Hypochromic Microcytic Anemia 36 1.152
926
P PRR002 Pure Red-Cell Aplasia 46 1.152
927
PFF001 Pfeiffer Syndrome 77 1.143
928
c GLY004 Glycogen Storage Disease V 62 1.142
929
HMT020 Hematopoietic Stem Cell Kinetics, Control of 8 1.141
930
6PH002 6-Phosphogluconolactonase Deficiency 9 1.141
931
TRN030 Transient Erythroblastopenia of Childhood 34 1.141
932
HND002 Hand, Foot and Mouth Disease 50 1.140
933
P HMP002 Hemophagocytic Lymphohistiocytosis 60 1.139
934
P ECT006 Ectodermal Dysplasia 62 1.139
935
PHR003 Pharyngitis 57 1.139
936
BNG077 Benign Idiopathic Neonatal Seizures 23 1.136
937
P END047 Endophthalmitis 53 1.134
938
P AVS003 Avascular Necrosis 41 1.133