Search results for Fructose 6-phosphate

794 hits were found for Fructose 6-phosphate

# Family MCID Name MIFTS Score
1
FRC011 Fructose Intolerance, Hereditary 55 78.206
2
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 68.505
3
FRC001 Fructose-1,6-Bisphosphatase Deficiency 50 60.512
4
c GLY060 Glycogen Storage Disease Ia 62 28.103
5
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 26.168
6
FRC013 Fructose Utilization 15 25.478
7
FTT001 Fatty Liver Disease 61 17.893
8
NNL005 Non-Alcoholic Fatty Liver Disease 63 17.501
9
P HML002 Hemolytic Anemia 62 14.462
10
GLC039 Glucosephosphate Isomerase Deficiency 17 14.279
11
HYP056 Hypoglycemia 65 13.103
12
HYP066 Hyperglycemia 60 12.912
13
HYP060 Hyperinsulinism 53 12.847
14
LPD008 Lipid Metabolism Disorder 61 12.727
15
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 12.683
16
P HYP750 Hypertriglyceridemia, Familial 61 11.966
17
P LVR013 Liver Disease 68 11.040
18
P GLY013 Glycogen Storage Disease 59 10.347
19
HYP014 Hyperuricemia 51 10.007
20
NNT012 Neonatal Jaundice 53 9.859
21
BLR008 Bilirubin Metabolic Disorder 57 9.354
22
GLC003 Glucose Intolerance 53 9.004
23
DFC004 Deficiency Anemia 74 8.976
24
NNL006 Non-Alcoholic Steatohepatitis 54 8.889
25
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 8.682
26
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 8.378
27
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 8.378
28
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 8.378
29
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 8.378
30
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 8.378
31
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 8.378
32
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 8.378
33
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 8.378
34
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 8.378
35
RPD005 Rapidly Involuting Congenital Hemangioma 48 8.316
36
MLR004 Malaria 77 8.241
37
FRC005 Fructosuria, Essential 37 7.323
38
c TYP009 Type 2 Diabetes Mellitus 91 6.655
39
GT001 Gout 63 6.081
40
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 5.915
41
P THL005 Thalassemia 56 5.807
42
P CTR002 Cataract 59 5.758
43
P KDN018 Kidney Disease 71 5.745
44
P SCK005 Sickle Cell Disease 56 5.741
45
ATS010 Autosomal Recessive Disease 42 5.667
46
c VRL010 Viral Hepatitis 52 5.568
47
P KRN004 Kernicterus 47 5.497
48
P MYP004 Myopathy 67 5.477
49
c TYP008 Type 1 Diabetes Mellitus 77 5.436
50
HYP266 Hypoxia 56 5.418
51
ANX004 Anoxia 40 5.307
52
MTB004 Metabolic Acidosis 48 5.285
53
P LCT001 Lactic Acidosis 50 5.057
54
48X005 48,xyyy 39 5.021
55
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 5.011
56
P DBT009 Diabetes Mellitus 67 4.953
57
DNT012 Dental Caries 53 4.886
58
SCK003 Sickle Cell Anemia 74 4.835
59
c INH020 Inherited Metabolic Disorder 47 4.753
60
c HPT003 Hepatitis a 63 4.747
61
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 48 4.681
62
P HPT021 Hepatitis 68 4.667
63
HLX001 Helix Syndrome 47 4.536
64
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.528
65
CNG017 Congenital Nonspherocytic Hemolytic Anemia 34 4.422
66
c HYP836 Hypercholesterolemia, Familial, 1 73 4.421
67
P INF032 Infertility 60 4.288
68
P OVR082 Overgrowth Syndrome 41 4.257
69
P GLC113 Galactosemia I 65 4.168
70
c MCR133 Microvascular Complications of Diabetes 4 41 4.145
71
c MCR113 Microvascular Complications of Diabetes 3 52 4.145
72
c MCR130 Microvascular Complications of Diabetes 6 41 4.145
73
c MCR120 Microvascular Complications of Diabetes 7 47 4.145
74
P MCL001 Mucolipidosis 49 4.114
75
P MSC005 Muscular Dystrophy 66 4.097
76
IRN002 Iron Metabolism Disease 56 3.996
77
LVR012 Liver Cirrhosis 62 3.951
78
GLY111 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency Type Ib 36 3.938
79
c ACT071 Acute Kidney Failure 60 3.899
80
P ART022 Arthritis 70 3.879
81
c HYP595 Hypertension, Essential 84 3.835
82
LYS002 Lysosomal Storage Disease 51 3.776
83
GLM045 Glioma 62 3.680
84
GLL048 Glial Tumor 51 3.669
85
GLB002 Glioblastoma 67 3.662
86
P MLN007 Male Infertility 56 3.640
87
c CHR684 Chronic Kidney Disease 73 3.558
88
INS024 Insulin-Like Growth Factor I 77 3.544
89
CLN015 Colon Adenocarcinoma 64 3.514
90
RNL114 Renal Cell Carcinoma, Nonpapillary 79 3.496
91
AGN016 Aging 53 3.440
92
c CNG411 Congenital Disorder of Glycosylation, Type in 66 3.426
93
ISC004 Ischemia 61 3.412
94
PRT037 Pertussis 49 3.378
95
P CRN300 Coronary Heart Disease 1 73 3.376
96
c GLY008 Glycogen Storage Disease Ii 72 3.376
97
GLB001 Gilbert Syndrome 53 3.367
98
c MCR115 Microvascular Complications of Diabetes 5 65 3.356
99
P MLN008 Melanoma 75 3.347
100
BCT022 Bacterial Infectious Disease 55 3.345
101
P HPT023 Hepatocellular Carcinoma 95 3.311
102
P BRS047 Breast Cancer 97 3.281
103
PPL052 Papillomatosis, Confluent and Reticulated 34 3.264
104
47X002 47,xyy 47 3.251
105
ALC007 Alcohol Dependence 65 3.243
106
P LCT002 Lactose Intolerance 51 3.239
107
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.232
108
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 3.230
109
P HYP086 Hypothyroidism 68 3.226
110
P MYC084 Mycobacterium Tuberculosis 1 68 3.161
111
P DRR001 Diarrhea 55 3.160
112
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 3.078
113
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.023
114
c ACT134 Acute Liver Failure 57 3.022
115
P HYP076 Hyperthyroidism 53 3.018
116
BNR002 Bone Resorption Disease 47 2.988
117
P RHM011 Rheumatoid Arthritis 81 2.979
118
P PLY011 Polycystic Ovary Syndrome 57 2.961
119
P RNL007 Renal Tubular Acidosis 52 2.958
120
P SZR006 Seizure Disorder 69 2.952
121
CRB039 Cerebrovascular Disease 65 2.931
122
URM002 Uremia 47 2.928
123
HMS001 Hemosiderosis 48 2.914
124
P RRH023 Rare Hereditary Hemochromatosis 52 2.914
125
P CLC063 Celiac Disease 1 65 2.867
126
P CHR012 Chronic Granulomatous Disease 69 2.866
127
P ENC018 Encephalopathy 62 2.839
128
CHY002 Chylomicron Retention Disease 64 2.838
129
PST011 Pustulosis of Palm and Sole 52 2.825
130
P PSR002 Psoriasis 63 2.825
131
P NTR004 Neutropenia 62 2.817
132
CHL123 Chlamydia 58 2.813
133
P LNG032 Lung Cancer 98 2.791
134
CHL068 Cholestasis 61 2.787
135
P PNC035 Pancreatic Cancer 87 2.763
136
P NRB001 Neuroblastoma 66 2.758
137
P NRP001 Neuropathy 59 2.747
138
FST010 Fasting Hypoglycemia 33 2.742
139
CYT002 Cytokine Deficiency 43 2.734
140
OCL069 Ocular Motor Apraxia 57 2.711
141
TYP007 Typhoid Fever 63 2.705
142
PRT251 Proteinuria, Chronic Benign 58 2.701
143
c SPR086 Spermatogenic Failure 3 47 2.696
144
CLR030 Clear Cell Renal Cell Carcinoma 53 2.696
145
ATH013 Atherosclerosis Susceptibility 63 2.696
146
P HRT032 Heart Disease 84 2.688
147
PHN003 Phenylketonuria 76 2.673
148
SLP001 Sleeping Sickness 56 2.667
149
P KLZ004 Kala-Azar 1 41 2.614
150
LSH001 Leishmaniasis 63 2.614
151
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.591
152
P ALZ034 Alzheimer Disease 87 2.589
153
RNL077 Renal Fibrosis 46 2.585
154
c PRC016 Pre-Eclampsia 64 2.576
155
P ADN016 Adenocarcinoma 63 2.574
156
GST033 Gestational Diabetes 60 2.565
157
P CLR023 Colorectal Cancer 100 2.556
158
P FBR017 Fibrosarcoma 55 2.525
159
P OVR042 Ovarian Cancer 88 2.498
160
P VSC007 Vascular Disease 62 2.493
161
URT049 Urate Oxidase, Pseudogene 24 2.483
162
P AST005 Asthma 75 2.482
163
SPL018 Splenomegaly 47 2.478
164
P LKM002 Leukemia 65 2.476
165
P CND004 Candidiasis 57 2.473
166
ALL029 Allergic Disease 61 2.473
167
P ALC033 Alcohol Use Disorder 67 2.470
168
HPT019 Hepatic Encephalopathy 59 2.453
169
CHL014 Cholera 62 2.445
170
PST092 Posttransplant Acute Limbic Encephalitis 29 2.424
171
P PLM037 Pulmonary Hypertension 69 2.423
172
OVR063 Overnutrition 42 2.416
173
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.408
174
DBT010 Diabetic Neuropathy 54 2.387
175
P MYL006 Myeloid Leukemia 60 2.375
176
P PLM036 Pulmonary Fibrosis 65 2.375
177
HMN044 Human Immunodeficiency Virus Type 1 76 2.371
178
c CNG027 Congenital Hemolytic Anemia 49 2.368
179
AZS001 Azoospermia 45 2.363
180
P LNG064 Lung Cancer Susceptibility 3 69 2.340
181
P GLM040 Glioma Susceptibility 1 70 2.332
182
P HRD011 Hereditary Spherocytosis 63 2.325
183
CHR074 Choriocarcinoma 46 2.319
184
SQM006 Squamous Cell Carcinoma 59 2.314
185
LNG099 Lung Disease 62 2.282
186
PRD004 Prediabetes Syndrome 52 2.267
187
HYP017 Hypophosphatemia 49 2.267
188
DBT007 Diabetic Cataract 36 2.264
189
DBT084 Diabetes Mellitus, Ketosis-Prone 59 2.248
190
LWC002 Lowe Oculocerebrorenal Syndrome 68 2.232
191
HMP009 Haemophilus Influenzae 41 2.224
192
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.208
193
NPH009 Nephrolithiasis 54 2.202
194
OST159 Osteogenic Sarcoma 66 2.194
195
CYS001 Cystic Fibrosis 77 2.194
196
c ATR087 Atrial Standstill 1 74 2.194
197
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 2.191
198
P MTR004 Maturity-Onset Diabetes of the Young 66 2.187
199
P ADL010 Adult Respiratory Distress Syndrome 70 2.168
200
SVN002 Sveinsson Chorioretinal Atrophy 45 2.167
201
INS001 Insulinoma 59 2.157
202
c LKM061 Leukemia, Acute Myeloid 83 2.154
203
HNS001 Hansen's Disease 32 2.153
204
CYN002 Cyanosis, Transient Neonatal 43 2.132
205
P PRS040 Prostate Cancer 95 2.131
206
P CNG001 Congenital Myasthenic Syndrome 68 2.126
207
LPT014 Leptin Deficiency or Dysfunction 77 2.123
208
P THR014 Thrombocytopenia 66 2.114
209
c HPT001 Hepatitis C 61 2.111
210
RYS001 Reye Syndrome 49 2.109
211
MSC157 Muscular Dystrophy, Duchenne Type 78 2.097
212
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.093
213
END086 End Stage Renal Disease 54 2.077
214
STT001 Status Epilepticus 58 2.073
215
CLT003 Colitis 63 2.052
216
P LPR021 Leprosy 3 71 2.050
217
DSS032 Disease by Infectious Agent 55 2.048
218
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.040
219
ATM095 Autoimmune Disease 61 2.016
220
HGH043 High Grade Glioma 46 2.013
221
P CRD246 Cardiovascular System Disease 55 2.007
222
P HRP006 Herpes Simplex 65 2.005
223
ACT098 Acute Erythroid Leukemia 55 2.003
224
HRW001 Hair Whorl 35 1.999
225
CHG001 Chagas Disease 65 1.989
226
HPT004 Hepatic Coma 43 1.972
227
c DLT002 Dilated Cardiomyopathy 79 1.971
228
HYP043 Hyperandrogenism 47 1.960
229
CRB004 Cerebral Artery Occlusion 45 1.953
230
P LKM062 Leukemia, Acute Lymphoblastic 69 1.951
231
ACT003 Acute Kidney Tubular Necrosis 46 1.949
232
IMP005 Impotence 52 1.924
233
P TYR004 Tyrosinemia 49 1.921
234
CRV035 Cervical Cancer 72 1.917
235
SRC014 Sarcoma 64 1.899
236
c SCL052 Scleroderma, Familial Progressive 60 1.898
237
VLV047 Volvulus of Midgut 55 1.884
238
P ASP006 Aspergillosis 71 1.878
239
TXC005 Toxic Shock Syndrome 61 1.876
240
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.873
241
ENT011 Enterocolitis 55 1.870
242
P GST053 Gastric Cancer 82 1.864
243
P PRP029 Porphyria 60 1.861
244
P MCR129 Microvascular Complications of Diabetes 1 67 1.860
245
P FNC004 Fanconi Syndrome 60 1.860
246
c PRG106 Progressive Muscular Dystrophy 31 1.856
247
c SML038 Small Cell Cancer of the Lung 68 1.847
248
DWN001 Down Syndrome 70 1.846
249
P HMC002 Homocystinuria 52 1.841
250
PLY150 Polykaryocytosis Inducer 29 1.838
251
ATN005 Autonomic Dysfunction 45 1.837
252
VRL011 Viral Infectious Disease 60 1.819
253
DSS009 Disseminated Intravascular Coagulation 56 1.811
254
P MSC003 Muscular Atrophy 52 1.804
255
FML035 Familial Hyperlipidemia 54 1.800
256
STM007 Stomatitis 52 1.784
257
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.780
258
CHL147 Chlamydia Pneumonia 47 1.771
259
P ECL001 Eclampsia 52 1.771
261
SNL007 Senile Cataract 40 1.749
262
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 26 1.749
263
RCK004 Rickets 64 1.749
264
CHL004 Cholelithiasis 48 1.749
265
P ACN011 Acne 55 1.747
266
ART140 Arteries, Anomalies of 52 1.747
267
LPP008 Lipoprotein Quantitative Trait Locus 65 1.747
268
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.741
269
c ACT027 Acute Pancreatitis 60 1.716
270
P INF037 Inflammatory Bowel Disease 53 1.676
271
CVD001 Covid-19 59 1.671
272
c THY107 Thymoma, Familial 42 1.664
273
P THY023 Thymoma 64 1.664
274
VRC001 Varicocele 48 1.659
275
P KDN017 Kidney Cancer 60 1.659
276
P CRD119 Cardiac Arrest 68 1.656
277
SKN016 Skin Disease 63 1.654
278
BRC012 Brucellosis 66 1.637
279
PRC002 Paracoccidioidomycosis 53 1.637
280
PLM010 Pulmonary Edema 54 1.637
281
GST045 Gastroenteritis 58 1.635
282
P MYG005 Myoglobinuria 40 1.633
283
SBC016 Subacute Delirium 42 1.629
284
IRN001 Iron Deficiency Anemia 58 1.628
285
c PCH010 Pachyonychia Congenita 3 43 1.625
286
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.623
287
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.623
288
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.620
289
SCH014 Schistosomiasis 56 1.620
290
ACQ007 Acquired Immunodeficiency Syndrome 58 1.611
291
CRB037 Cerebral Palsy 66 1.609
292
P ALP008 Alopecia 53 1.605
293
SYN007 Synovitis 54 1.602
294
PLC002 Plica Syndrome 35 1.602
295
P RTN018 Retinal Disease 53 1.597
296
P ANP001 Anaplastic Large Cell Lymphoma 59 1.588
297
MNT002 Mental Depression 56 1.586
298
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.585
299
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 1.578
300
FLR002 Filariasis 55 1.577
301
STR067 Stroke, Ischemic 79 1.577
302
ULC004 Ulcerative Colitis 74 1.569
303
CRB090 Cerebral Hypoxia 42 1.569
304
CLN003 Clonorchiasis 42 1.559
305
PRN019 Perinatal Necrotizing Enterocolitis 60 1.555
306
BRN024 Bronchitis 67 1.551
307
MSC007 Muscle Hypertrophy 64 1.549
308
KRT002 Keratomalacia 54 1.542
309
TRN015 Transient Cerebral Ischemia 62 1.539
310
P PLY018 Polycythemia 56 1.529
311
c ACT075 Acute Myocardial Infarction 55 1.529
312
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.527
313
TRT001 Teratocarcinoma 41 1.521
314
BRN004 Brain Edema 54 1.520
315
ANX010 Anxiety 70 1.515
316
MNN043 Meningioma, Familial 79 1.512
317
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.512
318
SCR001 Secretory Meningioma 40 1.512
319
INT395 Intracranial Meningioma 47 1.512
320
P MCR010 Microcephaly 59 1.504
321
P PRP019 Peripheral Nervous System Disease 57 1.491
322
c MJR022 Major Affective Disorder 8 37 1.486
323
c MJR024 Major Affective Disorder 9 40 1.486
324
P BPL003 Bipolar Disorder 56 1.486
325
c HPT016 Hepatitis B 62 1.484
326
IMM167 Immune Deficiency Disease 76 1.477
327
P GCH001 Gaucher's Disease 69 1.475
328
RTN020 Retinal Vascular Disease 45 1.470
329
PLM001 Pulmonary Tuberculosis 69 1.450
330
FNC009 Fanconi-Bickel Syndrome 53 1.449
331
P RHB003 Rhabdomyosarcoma 66 1.449
332
ESP021 Esophageal Cancer 84 1.448
333
HYP080 Hypogonadism 49 1.446
334
CYS010 Cystinosis 61 1.444
335
CRH001 Crohn's Disease 80 1.439
336
TRY001 Trypanosomiasis 50 1.428
337
VSC003 Visceral Leishmaniasis 54 1.424
338
P WSK001 Wiskott-Aldrich Syndrome 72 1.423
339
P OBS001 Obstructive Jaundice 49 1.416
340
P HYP050 Hyperinsulinemic Hypoglycemia 56 1.405
341
c MCP050 Mucopolysaccharidosis, Type Ii 73 1.395
342
CHL065 Cholangiocarcinoma 57 1.389
343
INT079 Intrahepatic Cholangiocarcinoma 51 1.389
344
c CTR185 Cataract 30 31 1.384
345
PCK003 Pick Disease of Brain 70 1.382
346
c GLL024 Gallbladder Disease 1 53 1.382
347
P NMN002 Niemann-Pick Disease 60 1.382
348
P BRS044 Breast Adenocarcinoma 58 1.375
349
c GLC079 Glaucoma 1, Open Angle, P 23 1.372
350
DBT008 Diabetic Angiopathy 47 1.370
351
BRN071 Brain Injury 50 1.359
352
URL001 Urolithiasis 45 1.355
353
P RNL015 Renal Hypertension 45 1.354
354
c HMC039 Hemochromatosis, Type 1 73 1.351
355
PRC013 Pericarditis 53 1.350
356
P OPT006 Optic Nerve Disease 57 1.348
357
P ATX030 Ataxia-Telangiectasia 80 1.344
358
TLN003 Telangiectasis 51 1.344
359
HMC014 Homocysteinemia 52 1.343
360
P PLY019 Polyneuropathy 52 1.340
361
THL010 Thalassemia Minor 30 1.332
362
SPN035 Spindle Cell Sarcoma 51 1.331
363
GRW007 Growth Hormone Deficiency 47 1.330
364
c MCR112 Microvascular Complications of Diabetes 2 42 1.330
365
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 61 1.324
367
P SLM003 Salmonellosis 54 1.323
368
CHL067 Cholecystitis 59 1.323
369
ART004 Aortic Atherosclerosis 46 1.319
370
P MLG056 Malignant Hyperthermia 65 1.313
371
ALP103 Alpha-1-Antitrypsin Deficiency 67 1.310
372
PSR001 Psoriatic Arthritis 61 1.308
373
NPH003 Nephrocalcinosis 49 1.303
374
PLY001 Polycythemia Vera 69 1.294
375
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.294
376
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.293
377
MYL069 Myeloma, Multiple 76 1.284
378
TNG007 Tongue Carcinoma 55 1.283
379
ENT004 Enthesopathy 51 1.283
380
P TXP001 Toxoplasmosis 59 1.282
381
c GRV008 Graves Disease 1 54 1.281
382
GRD001 Giardiasis 46 1.277
383
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.275
384
BTN004 Biotin Deficiency 44 1.274
385
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.264
386
THY006 Thymus Lymphoma 27 1.255
387
P HYP730 Hypogonadotropic Hypogonadism 57 1.253
388
ARG004 Argyria 26 1.249
389
c SPN225 Spondyloarthropathy 1 70 1.244
390
BRS099 Breast Ductal Carcinoma 61 1.244
391
SPN051 Spondylitis 51 1.244
392
INF009 Inflammatory Spondylopathy 30 1.244
394
c SVR003 Severe Congenital Neutropenia 59 1.240
395
P TRN020 Turner Syndrome 67 1.240
396
P VSC011 Vasculitis 61 1.237
397
MDD011 Mood Disorder 61 1.236
398
SDD001 Sudden Infant Death Syndrome 60 1.236
399
TRM010 Traumatic Brain Injury 50 1.228
400
P HRD144 Hereditary Mixed Polyposis Syndrome 54 1.228
401
INT066 Interstitial Lung Disease 60 1.222
402
MLG169 Malignant Astrocytoma 57 1.205
403
MLD001 Melioidosis 67 1.199
404
HYP026 Hypoglycemic Coma 37 1.197
405
SKN019 Skin Melanoma 70 1.191
406
P LKM071 Leukemia, Chronic Lymphocytic 74 1.182
407
c ACT068 Acute Cystitis 60 1.181
408
HYD038 Hydrops Fetalis, Nonimmune 57 1.151
409
c LYM150 Lymphatic Malformation 7 43 1.151
410
c LKM063 Leukemia, Chronic Myeloid 70 1.151
411
P PRK039 Parkinsonism 55 1.151
412
P TYS001 Tay-Sachs Disease 69 1.141
413
PRT036 Peritonitis 65 1.138
414
NRM005 Neuromuscular Disease 62 1.136
415
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.133
416
P LTR001 Lateral Sclerosis 57 1.133
417
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.133
418
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.133
419
P NSP012 Nasopharyngeal Carcinoma 60 1.127
420
P PRD008 Periodontitis 63 1.127
421
BCT021 Bacterial Sepsis 43 1.119
422
P DMN002 Dementia 65 1.117
423
BRS051 Breast Disease 58 1.112
424
MCR018 Microcytic Anemia 46 1.102
425
TTN003 Tetanus 64 1.098
426
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.090
427
WRN001 Werner Syndrome 69 1.089
428
THR004 Thrombocytosis 52 1.089
429
CHR178 Chromosomal Triplication 33 1.088
430
P SPP010 Suppressor of Tumorigenicity 3 50 1.080
431
P MLT020 Multiple Sclerosis 79 1.071
432
P MYT002 Myotonic Dystrophy 51 1.071
433
P HNT016 Huntington Disease 73 1.070
434
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.063
435
THR024 Thrombosis 56 1.060
436
OST012 Osteoarthritis 77 1.060
437
P FML187 Familial Hypertension 34 1.051
438
HRT011 Heart Septal Defect 49 1.048
439
P CRG003 Crigler-Najjar Syndrome, Type I 64 1.033
440
GLC008 Glucose Metabolism Disease 40 1.022
441
c MCL046 Mucolipidosis Iii Alpha/beta 61 1.022
442
WLS001 Wilson Disease 70 1.012
443
PRS045 Prostatic Hypertrophy 53 1.011
444
HPT022 Hepatoblastoma 54 1.009
445
MTB016 Metabolic Myopathy 30 1.006
446
c GLY011 Glycogen Storage Disease Vii 54 1.006
447
PRS021 Prostatic Adenoma 43 0.991
448
PRC051 Paracetamol Poisoning 29 0.991
449
MCP033 Mucopolysaccharidoses 44 0.984
450
GST092 Gastroesophageal Reflux 59 0.978
451
HYP020 Hyperprolactinemia 63 0.976
452
DWR001 Dwarfism 44 0.972
453
P BLD134 Bladder Cancer 79 0.970
454
PRS129 Prostatic Hyperplasia, Benign 48 0.968
455
MST005 Mastitis 52 0.968
456
P PRK057 Parkinson Disease, Late-Onset 79 0.965
457
c BRN108 Branchiootic Syndrome 1 63 0.962
458
THY029 Thyroid Carcinoma 55 0.957
459
HYP025 Hyperphosphatemia 47 0.953
460
P TRM003 Tremor 50 0.951
461
P XNT004 Xanthinuria 38 0.951
462
c HRD142 Hereditary Xanthinuria 44 0.951
463
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.950
464
c ERY067 Erythrocytosis, Familial, 8 34 0.946
465
P HYP061 Hypertrophic Cardiomyopathy 68 0.946
466
P MYC007 Myocardial Infarction 69 0.944
467
P BRB001 Beriberi 44 0.944
468
SVR001 Severe Acute Respiratory Syndrome 68 0.934
469
HYP141 Hyperphenylalaninemia 42 0.934
470
c HPT073 Hepatitis C Virus 70 0.932
471
LST001 Listeriosis 59 0.929
472
GTR002 Goiter 52 0.916
473
P RTN008 Retinitis Pigmentosa 79 0.915
474
NRR001 Neuroretinitis 42 0.915
475
P SYP003 Syphilis 59 0.915
476
RTN023 Retinitis 45 0.915
477
HYP005 Hypokalemia 55 0.913
478
CRD132 Cardiac Conduction Defect 59 0.903
479
PYR009 Pyridoxine Deficiency Anemia 35 0.903
480
P DNG005 Dengue Virus 55 0.897
481
DYS018 Dysostosis 43 0.897
482
PLG002 Plague 58 0.897
483
P EYD002 Eye Disease 57 0.896
484
STN013 Stenotrophomonas Maltophilia Infection 26 0.896
485
HVY002 Heavy Metal Poisoning 22 0.896
486
PPT005 Peptic Ulcer Disease 58 0.894
487
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.892
488
CRY005 Cryptococcosis 61 0.892
489
MYC019 Mycobacterium Marinum 29 0.892
490
LSC001 Lesch-Nyhan Syndrome 62 0.890
491
P AMY004 Amyloidosis 69 0.887
492
P FML011 Familial Adenomatous Polyposis 70 0.878
493
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.877
494
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.877
495
P DDN001 Duodenal Ulcer 52 0.877
496
VCC001 Vaccinia 49 0.877
497
BRN028 Brain Cancer 73 0.877
498
LYS030 Lysosomal Storage Disease with Skeletal Involvement 15 0.877
499
CNG429 Congenital Myasthenic Syndromes with Glycosylation Defect 34 0.876
500
MTH071 Methane Production 24 0.875
501
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.872
502
HYP264 Hypertonia 35 0.872
503
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.872
504
CRT015 Carotid Artery Occlusion 45 0.870
505
LPR001 Lepromatous Leprosy 49 0.866
506
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.865
507
TRN018 Transitional Cell Carcinoma 56 0.865
508
P SYS005 Systemic Scleroderma 73 0.865
509
SNS003 Sensory Peripheral Neuropathy 51 0.865
510
P ART021 Arteriosclerosis 53 0.858
511
P HYP098 Hypereosinophilic Syndrome 66 0.858
512
ADN018 Adenoma 58 0.857
513
P PNM007 Pneumonia 64 0.854
514
PLM033 Pulmonary Embolism 58 0.854
515
P INF038 Influenza 68 0.854
516
TST015 Testicular Disease 42 0.852
517
P DRM053 Dermatitis, Atopic 65 0.850
518
SCB001 Scabies 49 0.850
519
OTT002 Otitis Media 70 0.847
520
c ATS007 Autism Spectrum Disorder 71 0.839
521
HYP003 Hypermethioninemia 51 0.837
522
P MYC008 Myocarditis 59 0.836
523
P ENC004 Encephalitis 61 0.836
524
PRP001 Propionic Acidemia 65 0.832
525
c PRG020 Paragangliomas 3 39 0.828
526
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.828
527
ONC002 Onchocerciasis 50 0.828
528
GNG006 Gingival Hypertrophy 33 0.828
529
ALB002 Albinism 46 0.828
530
SYN036 Syncope 44 0.828
531
ORL015 Oral Squamous Cell Carcinoma 43 0.821
532
GLS001 Gliosarcoma 63 0.821
533
P HYP024 Hypoparathyroidism 55 0.821
534
CRD137 Cardiogenic Shock 56 0.821
535
KDN013 Kidney Hypertrophy 33 0.816
536
MNG006 Monogenic Diabetes 45 0.816
537
P VNT002 Ventricular Septal Defect 58 0.811
538
VLK001 Volkmann Contracture 23 0.811
539
END057 Endometrial Cancer 76 0.810
540
P RSP003 Respiratory Failure 73 0.806
541
AMN006 Aminoaciduria 37 0.801
542
PST028 Post-Traumatic Stress Disorder 58 0.799
543
ACT181 Acute Motor Axonal Neuropathy 25 0.799
544
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 0.797
545
DBN001 Dubin-Johnson Syndrome 58 0.797
546
OST017 Osteomyelitis 63 0.797
547
LWG006 Low Grade Glioma 41 0.797
548
P MTR014 Motor Neuron Disease 65 0.797
549
P PRR002 Pure Red-Cell Aplasia 46 0.797
550
PLR007 Pleural Empyema 50 0.797
551
P SKN015 Skin Carcinoma 71 0.797
552
LYM019 Lymphosarcoma 46 0.797
553
PTT037 Pituitary Tumors 44 0.797
554
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.796
555
P MTC133 Mitochondrial Myopathy 51 0.796
556
BTN003 Biotinidase Deficiency 61 0.785
557
DMP001 Dumping Syndrome 43 0.781
558
P SNS001 Sensorineural Hearing Loss 60 0.779
559
ALC006 Alcoholic Hepatitis 61 0.779
560
P ATS364 Autism 72 0.761
561
LMB062 Limb Ischemia 55 0.761
562
P ANG015 Angioedema 56 0.761
563
P SPN052 Spondyloarthropathy 54 0.757
564
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.757
565
ANP005 Anaplastic Astrocytoma 59 0.757
566
CCC002 Coccidiosis 50 0.757
567
THY122 Thyroid Gland Cancer 59 0.757
568
P DYS154 Dystonia 64 0.757
569
SPR010 Sporotrichosis 45 0.757
570
NRM001 Neuromyelitis Optica 60 0.757
571
P MNN013 Meningitis 65 0.756
572
P NPH012 Nephrotic Syndrome 61 0.755
573
PRP027 Peripheral Vascular Disease 71 0.739
574
DRM006 Dermatitis 61 0.729
575
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.725
576
P TMP001 Temporal Lobe Epilepsy 49 0.725
577
EMB004 Embryonal Carcinoma 55 0.718
578
IMM080 Immunodeficiency 23 51 0.716
579
THY125 Thyroid Gland Medullary Carcinoma 48 0.715
580
P MPL001 Maple Syrup Urine Disease 69 0.715
581
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.715
582
ANR040 Aneurysm 60 0.715
583
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 0.715
584
P HYP265 Hypotonia 42 0.694
585
P PYL005 Pyelonephritis 56 0.687
586
GLY014 Glycerol Kinase Deficiency 48 0.685
587
ISV001 Isovaleric Acidemia 54 0.685
588
c GLY004 Glycogen Storage Disease V 62 0.685
589
MTC005 Mitochondrial Metabolism Disease 44 0.685
590
ILS001 Ileus 49 0.685
591
P CRC039 Coarctation of Aorta 46 0.661
592
P SDR002 Siderosis 42 0.661
593
MCL006 Macular Retinal Edema 56 0.661
594
CRV040 Cervix Carcinoma 50 0.661
595
c ACT073 Acute Leukemia 59 0.661
596
P HYP083 Hypopituitarism 51 0.661
597
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.648
598
c FNC027 Fanconi Anemia, Complementation Group a 80 0.647
599
TST044 Testicular Torsion 45 0.647
600
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.647
601
GLC106 Glucocorticoid Resistance, Generalized 47 0.647
602
THY030 Thyroid Gland Disease 50 0.647
603
SFT003 Soft Tissue Sarcoma 43 0.647
604
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.647
605
IMM140 Immunodeficiency 47 56 0.645
606
P PLG001 Pelger-Huet Anomaly 51 0.645
607
FCT008 Factitious Disorder 34 0.645
608
P RBL001 Rubella 58 0.594
609
HLC007 Helicobacter Pylori Infection 67 0.588
610
P GLM007 Glomerulonephritis 59 0.582
611
c GLY003 Glycogen Storage Disease Iii 60 0.551
612
DYS015 Dysentery 49 0.549
613
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.527
614
MTH009 Mouth Disease 57 0.488
615
P BCL017 B-Cell Lymphoma 57 0.482
616
P RNL017 Renal Oncocytoma 54 0.473
617
c CNG415 Congenital Disorder of Glycosylation, Type Ia 58 0.451
618
LYM027 Lymphopenia 56 0.440
619
P THY032 Thyroiditis 56 0.440
620
PHS018 Phosphorylase Kinase Deficiency 37 0.440
621
P END033 Endocarditis 58 0.436
622
PRT013 Portal Hypertension 59 0.429
623
HPT067 Hepatocellular Adenoma 42 0.427
624
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.422
625
INF034 Infective Endocarditis 53 0.420
626
P PHC003 Pheochromocytoma 70 0.420
627
ADR040 Adrenal Gland Pheochromocytoma 45 0.420
628
ORL011 Oral Cancer 60 0.420
629
NRL016 Neural Tube Defects 80 0.420
630
PLY100 Polyploidy 36 0.420
631
TRN021 Transaldolase Deficiency 43 0.416
632
HND002 Hand, Foot and Mouth Disease 50 0.404
633
DPH001 Diphtheria 59 0.398
634
KLD004 Keloid Disorder 38 0.381
635
c MYS074 Myasthenic Syndrome, Congenital, 12 47 0.378
636
P RTN024 Retinoblastoma 72 0.374
637
TBL029 Tubulin, Beta 28 0.374
638
P ESS003 Essential Thrombocythemia 68 0.365
639
P GRV001 Graves' Disease 54 0.365
640
P RTN016 Retinal Degeneration 52 0.365
641
PYD002 Pyoderma 49 0.363
642
DPR016 Depression 64 0.363
643
PNC129 Pancreatic Adenocarcinoma 64 0.353
644
PRT038 Protein-Energy Malnutrition 53 0.353
645
LRN003 Learning Disability 49 0.352
646
c SYS001 Systemic Lupus Erythematosus 85 0.347
647
c THY056 Thyroid Dyshormonogenesis 3 32 0.347
648
P LPS004 Lupus Erythematosus 61 0.347
649
PRM329 Premature Aging 36 0.347
650
GNG013 Gingivitis 59 0.343
651
PLC005 Placental Insufficiency 55 0.341
652
VSC002 Vascular Dementia 59 0.327
653
P CRP001 Carpal Tunnel Syndrome 65 0.324
654
HML052 Hemolytic Anemia, Nonspherocytic, Due to Hexokinase Deficiency 26 0.324
655
MLD018 Mild Cognitive Impairment 48 0.324
656
ADG002 Audiogenic Seizures 25 0.324
657
PRX001 Peroxisomal Disease 46 0.323
658
HYP457 Hypertrophic Scars 42 0.322
659
PRP030 Purpura 54 0.308
660
ALC010 Alcoholic Cardiomyopathy 42 0.308
661
c ACT004 Acute Diarrhea 40 0.304
662
ABT001 Abetalipoproteinemia 68 0.304
663
P MJR001 Major Depressive Disorder 68 0.304
664
P PTS002 Ptosis 52 0.298
665
CNG034 Congestive Heart Failure 69 0.298
666
P AGM001 Agammaglobulinemia 67 0.298
667
CHR182 Chromosome 10p Duplication 24 0.298
668
MYC005 Myocardial Stunning 45 0.298
669
CRT072 Creutzfeldt-Jakob Disease 67 0.297
670
c FML021 Familial Hypercholesterolemia 71 0.297
671
FCS002 Fucosidosis 61 0.286
672
URD002 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to 26 0.286
673
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.286
674
KPS004 Kaposi Sarcoma 76 0.286
675
c LKM070 Leukemia, Acute Monocytic 56 0.286
676
QFV001 Q Fever 61 0.286
677
P EPL164 Epilepsy 70 0.286
678
ACT200 Acute Monoblastic Leukemia 40 0.286
679
P MNC007 Monocytic Leukemia 48 0.286
680
P MYC033 Myoclonus 46 0.286
681
PRT019 Protein-Losing Enteropathy 44 0.282
682
c ATM011 Autoimmune Hepatitis 62 0.282
683
SMN007 Seminoma 42 0.282
684
P GST044 Gastritis 55 0.282
685
P MTC069 Mitochondrial Disorders 57 0.282
686
CHP002 Chops Syndrome 47 0.267
687
P MVM001 Movement Disease 61 0.267
688
BNG077 Benign Idiopathic Neonatal Seizures 23 0.267
689
P SCL048 Sclerosteosis 58 0.260
690
ORT008 Orotic Aciduria 56 0.260
691
OST003 Osteonecrosis 60 0.260
692
P OVR049 Ovarian Disease 50 0.260
693
CRC021 Carcinosarcoma 62 0.260
694
P TRT010 Teratoma 50 0.260
695
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.260
696
DST006 Diastolic Heart Failure 45 0.260
697
PRQ002 Paraquat Poisoning 28 0.260
698
c FST017 Fasting Plasma Glucose Level Quantitative Trait Locus 5 12 0.257
699
RTN003 Retinal Ischemia 48 0.257
700
GNT167 Genetic Obesity 33 0.257
701
HMM004 Hamamy Syndrome 39 0.229
702
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 0.229
703
P MDL005 Medulloblastoma 75 0.229
704
P EST010 Esterase B 13 0.229
705
c GLY007 Glycogen Storage Disease Iv 58 0.229
706
RST023 Resting Heart Rate, Variation in 40 0.229
708
KRT019 Keratitis, Hereditary 66 0.229
709
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 0.229
710
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 0.229
711
HRN029 Hearing Loss, Noise-Induced 37 0.229
712
P FTL001 Fetal Alcohol Syndrome 55 0.229
713
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.229
714
CMB007 Combined Immunodeficiency 56 0.229
715
TLR001 Tularemia 56 0.229
716
P LRY044 Larynx Cancer 53 0.229
717
PNC034 Pancreas Disease 49 0.229
718
ERL001 Early Myoclonic Encephalopathy 62 0.229
719
ECH003 Echinococcosis 52 0.229
720
FSC002 Fascioliasis 43 0.229
721
BCK006 Back Pain 43 0.229
722
SPR033 Superficial Spreading Melanoma 25 0.229
723
INF118 Inflammatory Myopathy with Abundant Macrophages 27 0.229
724
OVR094 Ovarian Epithelial Cancer 39 0.229
725
P MRC003 Mercury Poisoning 48 0.229
726
GLY010 Glycine Encephalopathy 57 0.227
727
RTN017 Retinal Detachment 60 0.227
728
c MGR028 Migraine with or Without Aura 1 63 0.227
729
MNK001 Menkes Disease 64 0.227
730
ANN002 Anencephaly 57 0.227
731
c TBR025 Tuberous Sclerosis 1 84 0.227
732
P GRF003 Graft-Versus-Host Disease 71 0.227
733
TRS021 Triosephosphate Isomerase Deficiency 44 0.227
734
IGR001 Ige Responsiveness, Atopic 58 0.227
735
P CRB045 Cerebellar Hypoplasia 40 0.227
736
BRR014 Barrett Esophagus 66 0.227
737
CYS009 Cystadenoma 42 0.227
738
P TBR001 Tuberous Sclerosis 69 0.227
739
KWS001 Kwashiorkor 44 0.227
740
RHM028 Rheumatic Heart Disease 55 0.227
741
RTC003 Root Caries 33 0.227
742
MCR011 Microinvasive Gastric Cancer 41 0.227
743
P ATR005 Atrophic Gastritis 50 0.227
744
P CHL066 Cholangitis 51 0.227
745
PRT058 Pure Autonomic Failure 58 0.227
746
XLN085 X-Linked Complicated Spastic Paraplegia Type 1 21 0.227
747
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 0.227
748
ATM060 Autoimmune Atrophic Gastritis 19 0.227
749
MYT011 Myotonia 37 0.227
750
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.189
751
CRH005 Crohn's Colitis 53 0.189
752
ACT149 Acetaminophen Metabolism 37 0.189
753
P MYP087 Myopathy, Tubular Aggregate, 1 49 0.189
754
PRX092 Peroxidase, Salivary 8 0.189
755
P MJR007 Major Affective Disorder 1 42 0.189
756
c SYN084 Synpolydactyly 1 36 0.189
757
c EXD008 Exudative Vitreoretinopathy 1 71 0.189
758
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.189
759
c CNG189 Congenital Disorder of Glycosylation, Type Ib 40 0.189
760
c NNN025 Noonan Syndrome 10 32 0.189
761
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.189
762
GLY015 Glycine N-Methyltransferase Deficiency 40 0.189
763
c THR092 Thrombophilia Due to Thrombin Defect 74 0.189
764
P ALG028 Alagille Syndrome 1 73 0.189
765
ONC007 Oncocytoma 49 0.189
766
FSH003 Fish Allergy 30 0.189
767
MGC001 Megacolon 48 0.189
768
DSS010 Dissociative Disorder 39 0.189
769
P OLG002 Oligodendroglioma 66 0.189
770
PPL022 Papilloma 53 0.189
771
PNM001 Pneumocystosis 60 0.189
772
BRN014 Bronchopneumonia 52 0.189
773
LYM021 Lymphadenitis 55 0.189
774
URT010 Ureteral Obstruction 44 0.189
775
MST004 Mast Cell Neoplasm 41 0.189
776
P CNJ013 Conjunctivitis 66 0.189
777
FNG004 Fungal Meningitis 46 0.189
778
SQM002 Squamous Cell Papilloma 45 0.189
779
MYM001 Myoma 54 0.189
780
PLM031 Poliomyelitis 62 0.189
781
EXT007 Extracutaneous Mastocytoma 38 0.189
782
QDR001 Quadriplegia 49 0.189
783
P HYD006 Hydrocephalus 62 0.189
784
LMY002 Leiomyoma 51 0.189
785
P HYP035 Hypophosphatasia 61 0.189
786
P INT070 Intestinal Obstruction 57 0.189
787
ANT024 Anthrax Disease 57 0.189
788
P BRN022 Bronchiectasis 59 0.189
789
LPD009 Lipid Storage Disease 45 0.189
790
P DBT005 Diabetes Insipidus 54 0.189
791
c BCT007 Bacterial Meningitis 55 0.189
792
FML168 Familial Isolated Pituitary Adenoma 33 0.189
793
DGT004 Digitalis Poisoning 13 0.189
794
DYS073 Dysphagia 53 0.189
Content
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