Search results for Glycerol

1774 hits were found for Glycerol

# Family MCID Name MIFTS Score
1
GLY014 Glycerol Kinase Deficiency 48 57.589
2
GLY102 Glycerol Quantitative Trait Locus 13 31.146
3
GLY100 Glycerol Kinase 2 13 30.573
4
GLY101 Glycerol Kinase 3 Pseudogene 7 25.013
5
CHR387 Chromosome Xp21 Deletion Syndrome 36 23.445
6
BTG004 Beta-Glycerol Phosphatase 6 22.266
7
DSR071 Disorder of Glycerol Metabolism 4 18.568
8
c ACT071 Acute Kidney Failure 60 9.360
9
TRG002 Trigeminal Neuralgia 61 7.745
10
P KDN018 Kidney Disease 71 7.289
11
P MSC005 Muscular Dystrophy 66 5.074
12
HYP056 Hypoglycemia 65 5.009
13
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 4.856
14
P MNN013 Meningitis 65 4.819
15
FRC001 Fructose-1,6-Bisphosphatase Deficiency 50 4.765
16
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 4.595
17
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 4.595
18
MSC157 Muscular Dystrophy, Duchenne Type 78 4.593
19
c BCT007 Bacterial Meningitis 55 4.557
20
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.543
21
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 4.543
22
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.543
23
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 4.543
24
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.543
25
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 4.543
26
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 4.543
27
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.543
28
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.543
29
MNR012 Meniere Disease 55 4.392
30
ADR049 Adrenal Hypoplasia, Congenital 52 4.242
31
P HYP750 Hypertriglyceridemia, Familial 61 4.076
32
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.024
33
DRM006 Dermatitis 61 4.016
34
RPD005 Rapidly Involuting Congenital Hemangioma 48 3.915
35
FTT001 Fatty Liver Disease 61 3.888
36
P DRM053 Dermatitis, Atopic 65 3.699
37
HYP066 Hyperglycemia 60 3.695
38
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.611
39
BRN004 Brain Edema 54 3.559
40
c TYP009 Type 2 Diabetes Mellitus 91 3.547
41
48X005 48,xyyy 39 3.344
42
HYP060 Hyperinsulinism 53 3.285
43
INT075 Intracranial Hypertension 52 3.254
44
ALL029 Allergic Disease 61 3.230
45
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.152
46
OCL069 Ocular Motor Apraxia 57 3.141
47
MTH071 Methane Production 24 3.124
48
CNT047 Contact Dermatitis 56 3.093
49
CHL068 Cholestasis 61 3.066
50
HYP780 Hypoadrenocorticism, Familial 61 2.915
51
P MYP004 Myopathy 67 2.857
52
HMP009 Haemophilus Influenzae 41 2.852
53
P HDC001 Headache 56 2.789
54
ACT003 Acute Kidney Tubular Necrosis 46 2.702
55
P LVR013 Liver Disease 68 2.673
56
c STC015 Stickler Syndrome, Type I 50 2.669
57
URC002 Urea Cycle Disorder 51 2.621
58
TXC005 Toxic Shock Syndrome 61 2.603
59
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.578
60
P SNS001 Sensorineural Hearing Loss 60 2.548
61
MTB004 Metabolic Acidosis 48 2.523
62
IRN002 Iron Metabolism Disease 56 2.510
63
BRN071 Brain Injury 50 2.411
64
TRM010 Traumatic Brain Injury 50 2.408
65
P HYP076 Hyperthyroidism 53 2.382
66
LPD008 Lipid Metabolism Disorder 61 2.338
67
HLX001 Helix Syndrome 47 2.322
68
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.293
69
NRR001 Neuroretinitis 42 2.290
70
P HRD011 Hereditary Spherocytosis 63 2.290
71
RTN023 Retinitis 45 2.280
72
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.275
73
P TRN020 Turner Syndrome 67 2.233
74
P DBT009 Diabetes Mellitus 67 2.229
75
SLP001 Sleeping Sickness 56 2.217
76
P ENC018 Encephalopathy 62 2.202
77
GLL048 Glial Tumor 51 2.171
78
GLM045 Glioma 62 2.167
79
HYP266 Hypoxia 56 2.160
80
P MYC084 Mycobacterium Tuberculosis 1 68 2.121
81
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.120
82
c INH020 Inherited Metabolic Disorder 47 2.105
83
NSS002 Neisseria Meningitidis Infection 46 2.023
84
P GST053 Gastric Cancer 82 2.023
85
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.020
86
AGN016 Aging 53 2.006
87
CYS001 Cystic Fibrosis 77 1.999
88
P EYD002 Eye Disease 57 1.983
89
DFC004 Deficiency Anemia 74 1.967
90
c BRN108 Branchiootic Syndrome 1 63 1.933
91
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.922
92
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 1.895
93
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 1.895
94
HYP080 Hypogonadism 49 1.887
95
LVR012 Liver Cirrhosis 62 1.882
96
MNN020 Meningococcal Infection 44 1.876
97
HDN002 Head Injury 44 1.866
98
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.864
99
GST033 Gestational Diabetes 60 1.844
100
c ACT134 Acute Liver Failure 57 1.838
101
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.827
102
KRT019 Keratitis, Hereditary 66 1.823
103
MSC152 Muscular Dystrophy, Becker Type 69 1.815
104
P THL005 Thalassemia 56 1.811
105
P HYP730 Hypogonadotropic Hypogonadism 57 1.788
106
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 1.766
107
HPT019 Hepatic Encephalopathy 59 1.751
108
HPT004 Hepatic Coma 43 1.751
109
ANX004 Anoxia 40 1.732
110
MCL006 Macular Retinal Edema 56 1.728
111
ADR007 Adrenoleukodystrophy 73 1.726
112
ADR022 Adrenomyeloneuropathy 38 1.726
113
P ALC033 Alcohol Use Disorder 67 1.717
114
PRT037 Pertussis 49 1.686
115
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 1.672
116
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.653
117
HGH043 High Grade Glioma 46 1.639
118
INS024 Insulin-Like Growth Factor I 77 1.637
119
INS001 Insulinoma 59 1.632
120
SPN035 Spindle Cell Sarcoma 51 1.625
121
SRC014 Sarcoma 64 1.625
122
c HYP836 Hypercholesterolemia, Familial, 1 73 1.611
123
OCC001 Occupational Dermatitis 27 1.609
124
P SZR006 Seizure Disorder 69 1.605
125
P NTR004 Neutropenia 62 1.586
126
MCS002 Mucositis 55 1.581
127
GLB002 Glioblastoma 67 1.575
128
CRB004 Cerebral Artery Occlusion 45 1.575
129
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 1.573
130
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 1.560
131
ANG054 Angina Pectoris 65 1.552
132
P NRB001 Neuroblastoma 66 1.541
133
CRB039 Cerebrovascular Disease 65 1.540
134
P HYD006 Hydrocephalus 62 1.535
135
P HYP086 Hypothyroidism 68 1.535
136
c PRG106 Progressive Muscular Dystrophy 31 1.519
137
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 1.518
138
SKN016 Skin Disease 63 1.512
139
HRW001 Hair Whorl 35 1.507
140
TRY001 Trypanosomiasis 50 1.500
141
P MLT020 Multiple Sclerosis 79 1.488
142
TTN003 Tetanus 64 1.487
143
CVD001 Covid-19 59 1.483
144
47X002 47,xyy 47 1.479
145
P GLY013 Glycogen Storage Disease 59 1.469
146
LPT014 Leptin Deficiency or Dysfunction 77 1.466
147
c SPR086 Spermatogenic Failure 3 47 1.463
148
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 1.463
149
CHL014 Cholera 62 1.458
150
HYP555 Hypertriglyceridemia, Transient Infantile 39 1.445
151
DYS032 Dystrophinopathies 47 1.445
152
BRN024 Bronchitis 67 1.437
153
PTH003 Pathologic Nystagmus 52 1.429
154
CHG001 Chagas Disease 65 1.415
155
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.415
156
HMN044 Human Immunodeficiency Virus Type 1 76 1.408
157
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.398
158
CRT015 Carotid Artery Occlusion 45 1.386
159
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.386
160
PRT251 Proteinuria, Chronic Benign 58 1.378
161
P INT068 Intestinal Disease 53 1.368
162
P ASP006 Aspergillosis 71 1.362
163
ALN001 Aland Island Eye Disease 55 1.362
164
SPS057 Spasticity 43 1.346
165
c BTT014 Beta-Thalassemia 72 1.341
166
c GLY060 Glycogen Storage Disease Ia 62 1.340
167
ATS010 Autosomal Recessive Disease 42 1.338
168
ANT039 Antisynthetase Syndrome 55 1.337
170
P BRS047 Breast Cancer 97 1.322
171
P KLZ004 Kala-Azar 1 41 1.321
172
LSH001 Leishmaniasis 63 1.321
173
P LCT001 Lactic Acidosis 50 1.314
174
CTR172 Citrullinemia, Classic 64 1.312
175
AZS001 Azoospermia 45 1.312
176
KLB003 Klebsiella Pneumonia 49 1.303
177
P LNG032 Lung Cancer 98 1.294
178
P ALP106 Alport Syndrome 1, X-Linked 48 1.294
179
ATH013 Atherosclerosis Susceptibility 63 1.290
180
LYM017 Lyme Disease 63 1.286
181
STM007 Stomatitis 52 1.282
182
P NGH001 Night Blindness 52 1.276
183
ALB002 Albinism 46 1.276
184
BLR008 Bilirubin Metabolic Disorder 57 1.268
185
PLM010 Pulmonary Edema 54 1.268
186
c GRV008 Graves Disease 1 54 1.265
187
c HYP595 Hypertension, Essential 84 1.265
188
PPL052 Papillomatosis, Confluent and Reticulated 34 1.257
189
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.253
190
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.245
191
P AST005 Asthma 75 1.243
192
NNL006 Non-Alcoholic Steatohepatitis 54 1.239
193
P OCL001 Ocular Albinism 47 1.238
194
NWB001 Newborn Respiratory Distress Syndrome 56 1.236
195
GLC003 Glucose Intolerance 53 1.221
196
PLY150 Polykaryocytosis Inducer 29 1.210
197
P MYG005 Myoglobinuria 40 1.210
198
CHL123 Chlamydia 58 1.208
199
RYS001 Reye Syndrome 49 1.208
200
PNM013 Pneumococcal Meningitis 43 1.200
201
P HRP006 Herpes Simplex 65 1.197
202
RHB024 Rhabdomyosarcoma 2 65 1.195
203
CND006 Candida Glabrata 29 1.191
204
P CRN300 Coronary Heart Disease 1 73 1.191
205
P INF032 Infertility 60 1.190
206
ALL010 Allergic Contact Dermatitis 55 1.187
207
P OTT001 Otitis Externa 43 1.182
208
GLC008 Glucose Metabolism Disease 40 1.175
209
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.174
210
MNN043 Meningioma, Familial 79 1.173
211
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.173
212
SCR001 Secretory Meningioma 40 1.173
213
INT395 Intracranial Meningioma 47 1.173
214
P CTR002 Cataract 59 1.173
215
MST005 Mastitis 52 1.170
216
P RCT021 Rectum Cancer 54 1.167
217
PST092 Posttransplant Acute Limbic Encephalitis 29 1.164
218
P ART022 Arthritis 70 1.158
219
c TYP008 Type 1 Diabetes Mellitus 77 1.157
220
c PRM093 Premature Ovarian Failure 7 47 1.153
221
PNG002 Pain Agnosia 51 1.149
222
CLT003 Colitis 63 1.147
223
MDD003 Middle Cerebral Artery Infarction 37 1.147
224
HMG002 Hemoglobinuria 50 1.145
225
c DRM054 Dermatitis, Atopic, 2 47 1.137
226
P RHM011 Rheumatoid Arthritis 81 1.135
227
ALC007 Alcohol Dependence 65 1.128
228
P CLS010 Cluster Headache 42 1.124
229
CMM005 Common Cold 55 1.122
230
P PRK057 Parkinson Disease, Late-Onset 79 1.108
231
c ACH020 Achromatopsia 2 48 1.106
232
P ACH003 Achromatopsia 61 1.106
233
P PRD008 Periodontitis 63 1.105
234
P ACN011 Acne 55 1.097
235
CYT005 Cytomegalovirus Retinitis 50 1.095
236
P PLY014 Polycystic Kidney Disease 71 1.094
237
P BRG001 Brugada Syndrome 69 1.090
238
VSC003 Visceral Leishmaniasis 54 1.090
239
CRB086 Cerebral Aneurysms 40 1.090
240
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.088
241
STR067 Stroke, Ischemic 79 1.088
242
BCT022 Bacterial Infectious Disease 55 1.081
243
ADN018 Adenoma 58 1.081
244
P PNC035 Pancreatic Cancer 87 1.081
245
P CLR019 Color Blindness 47 1.079
246
c FNC027 Fanconi Anemia, Complementation Group a 80 1.068
247
P HMP002 Hemophagocytic Lymphohistiocytosis 60 1.068
248
QLT002 Qualitative or Quantitative Defects of Dystrophin 20 1.068
249
MSC012 Muscular Dystrophy, Duchenne and Becker Type 33 1.068
250
CNG034 Congestive Heart Failure 69 1.065
251
P HRT032 Heart Disease 84 1.065
252
PSY004 Psychotic Disorder 66 1.065
253
DWN001 Down Syndrome 70 1.065
254
NTR005 Nutritional Deficiency Disease 60 1.065
255
URM002 Uremia 47 1.056
256
IRN001 Iron Deficiency Anemia 58 1.052
257
P PLY011 Polycystic Ovary Syndrome 57 1.051
258
CYT002 Cytokine Deficiency 43 1.047
259
CLR033 Color Vision Deficiency 41 1.044
260
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 1.038
261
P PRK039 Parkinsonism 55 1.038
262
HYP005 Hypokalemia 55 1.038
263
KRT006 Keratoconjunctivitis 53 1.031
264
P HNT016 Huntington Disease 73 1.029
265
GTR002 Goiter 52 1.024
266
ILS001 Ileus 49 1.024
267
c ATS007 Autism Spectrum Disorder 71 1.011
268
P EXN002 Exanthem 58 1.009
269
PRS120 Persistent Idiopathic Facial Pain 27 1.009
270
c INF145 Infantile Liver Failure Syndrome 1 44 1.003
271
ADL002 Adult Syndrome 69 1.003
272
c BLD140 Blood Group, I System 47 1.003
273
HMR039 Hemorrhage, Intracerebral 57 1.003
274
IRR003 Irritant Dermatitis 47 1.000
275
P MLN007 Male Infertility 56 1.000
276
P RHN004 Rhinitis 56 1.000
277
IRR002 Irritable Bowel Syndrome 64 1.000
278
P HYP265 Hypotonia 42 1.000
279
THY029 Thyroid Carcinoma 55 1.000
280
MLR004 Malaria 77 0.990
281
FST010 Fasting Hypoglycemia 33 0.990
282
SYN036 Syncope 44 0.990
283
VCC001 Vaccinia 49 0.990
284
IGR001 Ige Responsiveness, Atopic 58 0.988
285
BCT002 Bacterial Vaginosis 52 0.988
286
KRT001 Keratoconjunctivitis Sicca 49 0.988
287
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.980
288
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.980
289
THL010 Thalassemia Minor 30 0.974
290
c GLC114 Glaucoma, Primary Closed-Angle 36 0.969
291
P LPR021 Leprosy 3 71 0.969
292
P ANP001 Anaplastic Large Cell Lymphoma 59 0.969
293
NRT004 Neuritis 53 0.969
294
HNS001 Hansen's Disease 32 0.969
295
WLL004 Wallerian Degeneration 38 0.969
296
APH001 Aphthous Stomatitis 57 0.961
297
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.959
298
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.959
299
c ACH038 Achromatopsia 7 38 0.959
300
AMD002 Amed Syndrome, Digenic 36 0.959
301
TRT020 Tritanopia 49 0.959
302
HYP458 Hyper Ige Syndrome 60 0.959
303
VGN023 Vaginitis 56 0.959
304
INT253 Intestinal Benign Neoplasm 46 0.959
305
ATX019 Ataxia with Vitamin E Deficiency 44 0.959
306
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 0.959
307
CHR682 Chronic Bilirubin Encephalopathy 37 0.959
308
RNL077 Renal Fibrosis 46 0.958
309
ORL015 Oral Squamous Cell Carcinoma 43 0.958
310
P ICH004 Ichthyosis 56 0.958
311
GLS004 Glossopharyngeal Neuralgia 37 0.954
312
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.934
313
GST045 Gastroenteritis 58 0.934
314
VST001 Vestibular Neuronitis 33 0.934
315
PLM031 Poliomyelitis 62 0.922
316
P ZLL001 Zellweger Syndrome 65 0.922
317
P CHR345 Chronic Pain 50 0.922
318
P ANR048 Aniridia 1 66 0.918
319
EWN003 Ewing Sarcoma 69 0.918
320
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 58 0.918
321
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.918
322
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.918
323
P MLG074 Malignant Mesenchymoma 40 0.918
324
HYP081 Hypolipoproteinemia 49 0.918
325
P DNT007 Dentin Sensitivity 35 0.918
326
SFT003 Soft Tissue Sarcoma 43 0.918
327
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.918
328
KRT009 Keratosis 52 0.910
329
P DBT005 Diabetes Insipidus 54 0.910
330
OVR063 Overnutrition 42 0.909
331
PPL021 Papilledema 49 0.909
332
P THR014 Thrombocytopenia 66 0.909
333
SCB001 Scabies 49 0.909
334
ORL011 Oral Cancer 60 0.909
335
ISC004 Ischemia 61 0.897
336
NRM004 Neuroma 49 0.895
337
c ACT068 Acute Cystitis 60 0.895
338
ANT024 Anthrax Disease 57 0.880
339
INF184 Infective Keratitis 13 0.880
340
P CRD119 Cardiac Arrest 68 0.877
341
OST159 Osteogenic Sarcoma 66 0.877
342
BNR002 Bone Resorption Disease 47 0.877
343
P SYP003 Syphilis 59 0.877
344
PRT036 Peritonitis 65 0.877
345
P MYC007 Myocardial Infarction 69 0.865
346
FCL007 Facial Neuralgia 28 0.865
347
HPT014 Hepatorenal Syndrome 49 0.865
348
BRN028 Brain Cancer 73 0.865
349
CRN309 Cranial Neuralgia 21 0.865
350
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.865
351
c STC013 Stickler Syndrome, Type Ii 36 0.860
352
P HPT023 Hepatocellular Carcinoma 95 0.855
353
PRD004 Prediabetes Syndrome 52 0.855
354
INV001 Invasive Aspergillosis 48 0.848
355
GRD001 Giardiasis 46 0.848
356
PRL008 Paralytic Ileus 44 0.848
357
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.842
358
P ANG015 Angioedema 56 0.830
359
c HRD002 Hereditary Angioedema 61 0.830
360
P CNG010 Congenital Stationary Night Blindness 56 0.823
361
BLM002 Bulimia Nervosa 56 0.823
362
P BLD134 Bladder Cancer 79 0.823
363
URT010 Ureteral Obstruction 44 0.823
364
P PRP029 Porphyria 60 0.823
365
P DRR001 Diarrhea 55 0.813
366
ANR040 Aneurysm 60 0.813
367
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.810
368
P ART021 Arteriosclerosis 53 0.810
369
DBT006 Diabetic Macular Edema 48 0.810
370
FSC004 Fasciitis 49 0.810
371
PRS063 Paresthesia 39 0.810
372
KRT002 Keratomalacia 54 0.805
373
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.803
374
PLG002 Plague 58 0.803
375
P VSC007 Vascular Disease 62 0.792
376
ART016 Aortic Aneurysm 68 0.792
377
P PRS040 Prostate Cancer 95 0.787
378
CCC002 Coccidiosis 50 0.787
379
GLC108 Gluconeogenesis Disorder 5 0.787
380
c PCH010 Pachyonychia Congenita 3 43 0.781
381
CRB037 Cerebral Palsy 66 0.781
382
PLR005 Pleuropneumonia 33 0.781
383
PRX001 Peroxisomal Disease 46 0.781
384
CNS004 Constipation 56 0.777
385
P FBR017 Fibrosarcoma 55 0.770
386
P MLN008 Melanoma 75 0.770
387
ACQ007 Acquired Immunodeficiency Syndrome 58 0.770
388
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.762
389
c BRG006 Brugada Syndrome 2 31 0.760
390
OCL006 Ocular Hypertension 53 0.760
391
P RTN008 Retinitis Pigmentosa 79 0.759
392
P GLM040 Glioma Susceptibility 1 70 0.759
393
MLG169 Malignant Astrocytoma 57 0.759
394
MYM001 Myoma 54 0.759
395
P TRT010 Teratoma 50 0.759
396
MNN009 Meningoencephalitis 47 0.759
397
P ART005 Arteriovenous Malformation 64 0.759
398
NRG002 Neurogenic Bladder 54 0.759
399
c ACT027 Acute Pancreatitis 60 0.748
400
ALL003 Allergic Rhinitis 66 0.747
401
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.747
402
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.747
403
PRP083 Porphyria, Acute Intermittent 64 0.747
404
DSS009 Disseminated Intravascular Coagulation 56 0.747
405
MDD018 Middle East Respiratory Syndrome 44 0.747
406
SPL018 Splenomegaly 47 0.747
407
P PNC044 Pancreatitis 61 0.738
408
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 0.735
409
P MTP001 Metaphyseal Dysplasia 38 0.735
410
XNT003 Xanthomatosis 48 0.734
411
LYD001 Leydig Cell Tumor 45 0.734
412
CRB090 Cerebral Hypoxia 42 0.734
413
c DWL002 Dowling-Degos Disease 1 58 0.721
414
LGN006 Legionnaire Disease 52 0.721
415
SQM006 Squamous Cell Carcinoma 59 0.721
416
OST012 Osteoarthritis 77 0.721
417
c HNT004 Huntington Disease-Like 2 51 0.707
418
P SLP006 Sleep Apnea 69 0.707
419
P NSP012 Nasopharyngeal Carcinoma 60 0.707
420
INT303 Intracranial Hypertension, Idiopathic 56 0.707
421
c THY056 Thyroid Dyshormonogenesis 3 32 0.707
422
c MCR115 Microvascular Complications of Diabetes 5 65 0.707
423
c HYP518 Hypogonadotropic Hypogonadism 16 with or Without Anosmia 27 0.707
424
FRC011 Fructose Intolerance, Hereditary 55 0.707
425
P LNG064 Lung Cancer Susceptibility 3 69 0.707
426
P BND020 Bone Disease 60 0.707
427
P RSP003 Respiratory Failure 73 0.707
428
TLR001 Tularemia 56 0.707
429
P RHZ001 Rhizomelic Chondrodysplasia Punctata 57 0.707
430
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.707
431
P INF037 Inflammatory Bowel Disease 53 0.706
432
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.700
433
P NRP001 Neuropathy 59 0.694
434
c AMY088 Amyotrophic Lateral Sclerosis 3 33 0.693
435
ASP007 Aspiration Pneumonia 49 0.693
436
VRC005 Varicose Veins 59 0.693
437
P RTN024 Retinoblastoma 72 0.693
438
c SML038 Small Cell Cancer of the Lung 68 0.693
439
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.693
440
P CRB045 Cerebellar Hypoplasia 40 0.693
441
SVR004 Severe Combined Immunodeficiency 70 0.693
442
TRN015 Transient Cerebral Ischemia 62 0.693
443
c ACT073 Acute Leukemia 59 0.693
444
P LBY004 Labyrinthitis 42 0.693
445
CRD137 Cardiogenic Shock 56 0.693
446
c HNT011 Huntington Disease-Like 3 33 0.677
447
HYP457 Hypertrophic Scars 42 0.677
448
P CRN026 Corneal Edema 42 0.677
449
c FML021 Familial Hypercholesterolemia 71 0.677
450
P BRS044 Breast Adenocarcinoma 58 0.677
451
TCK003 Tick-Borne Relapsing Fever 35 0.677
452
RLP003 Relapsing Fever 50 0.677
453
YLL002 Yellow Fever 61 0.677
454
P CRN028 Corneal Ulcer 47 0.677
455
P RTN016 Retinal Degeneration 52 0.677
456
MYC019 Mycobacterium Marinum 29 0.677
457
ALL014 Allergic Encephalomyelitis 34 0.677
458
HYP835 Hypothalamic Obesity 38 0.677
459
FBR047 Fibromyalgia 57 0.677
460
c RHZ011 Rhizomelic Chondrodysplasia Punctata, Type 1 53 0.661
461
c SPH013 Spherocytosis, Type 1 42 0.661
462
c GLC092 Glaucoma, Primary Open Angle 60 0.661
463
c SPH014 Spherocytosis, Type 2 38 0.661
464
P SLM003 Salmonellosis 54 0.661
465
NNT011 Neonatal Anemia 34 0.661
466
KWS001 Kwashiorkor 44 0.661
467
MDD010 Middle Ear Disease 46 0.661
468
P SKN015 Skin Carcinoma 71 0.661
469
P OPN001 Open-Angle Glaucoma 55 0.661
470
CHL122 Cholesteatoma of Middle Ear 51 0.661
471
BRR012 Berardinelli-Seip Congenital Lipodystrophy 26 0.661
472
P SCK005 Sickle Cell Disease 56 0.661
473
MYC015 Mycobacterium Fortuitum 28 0.661
474
P HPT021 Hepatitis 68 0.657
475
ENT011 Enterocolitis 55 0.643
476
PST011 Pustulosis of Palm and Sole 52 0.643
477
P PSR002 Psoriasis 63 0.643
478
GST092 Gastroesophageal Reflux 59 0.642
479
SCK003 Sickle Cell Anemia 74 0.642
480
URT049 Urate Oxidase, Pseudogene 24 0.642
481
c PRV019 Periventricular Nodular Heterotopia 1 37 0.642
482
P GRF003 Graft-Versus-Host Disease 71 0.642
483
BRK010 Burkitt Lymphoma 65 0.642
484
c VRL010 Viral Hepatitis 52 0.642
485
TYP007 Typhoid Fever 63 0.642
486
ANR004 Anuria 44 0.642
487
P CHR012 Chronic Granulomatous Disease 69 0.642
488
MDD011 Mood Disorder 61 0.642
489
BBS001 Babesiosis 48 0.642
490
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.642
491
FNG016 Fungal Keratitis 40 0.642
492
SDD008 Sudden Sensorineural Hearing Loss 41 0.642
493
PRM329 Premature Aging 36 0.642
494
c MJR022 Major Affective Disorder 8 37 0.628
495
c MJR024 Major Affective Disorder 9 40 0.628
496
P BPL003 Bipolar Disorder 56 0.628
497
ULC004 Ulcerative Colitis 74 0.628
498
LNG099 Lung Disease 62 0.628
499
ABD010 Abdominal Wall Defect 37 0.628
500
c PRD040 Periodontitis, Chronic 52 0.622
501
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.622
502
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.622
503
c THY107 Thymoma, Familial 42 0.622
504
P SPP010 Suppressor of Tumorigenicity 3 50 0.622
505
SDD001 Sudden Infant Death Syndrome 60 0.622
506
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.622
507
MTL005 Metal Allergy 40 0.622
508
P GCH001 Gaucher's Disease 69 0.622
509
P THY023 Thymoma 64 0.622
510
IMP005 Impotence 52 0.622
511
NWC001 Newcastle Disease 47 0.622
512
P INN002 Inner Ear Disease 49 0.622
513
PNC129 Pancreatic Adenocarcinoma 64 0.622
514
P NRM002 Normal Pressure Hydrocephalus 49 0.622
515
GT001 Gout 63 0.622
516
BRN018 Borna Disease 36 0.622
517
c ACT075 Acute Myocardial Infarction 55 0.622
518
SML019 Smallpox 55 0.622
519
EXP004 Exophthalmos 50 0.622
520
CRP032 Corpus Callosum, Agenesis of 49 0.615
521
CRT039 Corticosterone Methyloxidase Type I Deficiency 46 0.615
522
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.615
523
PYL017 Pyle Disease 37 0.615
524
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.615
525
P 46X052 46,xx Sex Reversal 1 54 0.615
526
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.615
527
ADP007 Adie Pupil 40 0.615
528
c DFN352 Deafness, Autosomal Recessive 8 37 0.615
529
c CNT035 Central Nervous System Disease 53 0.615
530
NNS042 Nonsyndromic Disorders of Testicular Development 21 0.615
531
VRL011 Viral Infectious Disease 60 0.615
532
46X012 46,xy Partial Gonadal Dysgenesis 41 0.615
533
MTY003 Mutyh Polyposis 39 0.615
534
ISL119 Isolated Optic Neuritis 27 0.615
535
HNM002 Hinman Syndrome 29 0.615
536
CHR459 Chromosome Xp Deletion 11 0.615
537
OTT002 Otitis Media 70 0.613
538
GST037 Gastroparesis 52 0.613
539
DRY001 Dry Eye Syndrome 49 0.613
540
P ALP008 Alopecia 53 0.613
541
DYS073 Dysphagia 53 0.613
542
ORG002 Organic Acidemia 43 0.600
543
c ALP105 Alport Syndrome 2, Autosomal Recessive 43 0.600
544
ARG002 Argininosuccinic Aciduria 61 0.600
545
SPR004 Supravalvular Aortic Stenosis 57 0.600
546
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.600
547
VRL003 Variola Major 43 0.600
548
HMF011 Hemifacial Spasm, Familial 33 0.600
549
MYL069 Myeloma, Multiple 76 0.600
550
INT258 Interstitial Nephritis, Karyomegalic 46 0.600
551
c HYP547 Hypogonadotropic Hypogonadism 12 with or Without Anosmia 33 0.600
552
HYP748 Hypertelorism 46 0.600
553
CLF027 Cleft Palate, Isolated 64 0.600
554
CMB007 Combined Immunodeficiency 56 0.600
555
HYP029 Hyperthyroxinemia 32 0.600
556
P END047 Endophthalmitis 53 0.600
557
MNC001 Monocular Esotropia 30 0.600
558
HMG005 Hemoglobinopathy 55 0.600
559
GNG013 Gingivitis 59 0.600
560
EMB004 Embryonal Carcinoma 55 0.600
561
ASP003 Aseptic Meningitis 50 0.600
562
HYP141 Hyperphenylalaninemia 42 0.600
563
CLF001 Cleft Lip 54 0.600
564
P TXP001 Toxoplasmosis 59 0.600
565
BCK006 Back Pain 43 0.600
566
EST005 Esotropia 43 0.600
567
NNT017 Neonatal Adrenoleukodystrophy 51 0.600
568
HGH041 High-Grade Astrocytoma 36 0.600
569
P FML355 Familial Intrahepatic Cholestasis 38 0.600
570
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.600
571
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.600
572
P HMF004 Hemifacial Spasm 38 0.600
573
CLF004 Cleft Lip/palate 56 0.600
574
ATN005 Autonomic Dysfunction 45 0.596
575
P ADL010 Adult Respiratory Distress Syndrome 70 0.578
576
c ALP101 Alpha-Thalassemia 62 0.573
577
P CTN015 Cutaneous T Cell Lymphoma 48 0.573
578
RTN017 Retinal Detachment 60 0.573
579
P MDL005 Medulloblastoma 75 0.573
580
PHS027 Phosphoglycoprotein 1 14 0.573
581
SPN354 Spinal Arachnoiditis 35 0.573
582
RFS006 Refsum Disease, Classic 63 0.573
583
WLS001 Wilson Disease 70 0.573
584
ICH001 Ichthyosis Vulgaris 53 0.573
585
P MMP001 Mumps 56 0.573
586
P CRN037 Craniosynostosis 67 0.573
587
THR004 Thrombocytosis 52 0.573
588
P BNC003 Bone Cancer 58 0.573
589
INT003 Intracranial Hypotension 36 0.573
590
CNJ007 Conjunctivochalasis 38 0.573
591
P CMM008 Communicating Hydrocephalus 44 0.573
592
BLL003 Bell's Palsy 48 0.573
593
ARC002 Arachnoiditis 49 0.573
594
P ACT046 Acute Apical Periodontitis 25 0.573
595
CHR013 Chronic Apical Periodontitis 32 0.573
596
SPN027 Spinal Stenosis 58 0.573
597
P MNC007 Monocytic Leukemia 48 0.573
598
RFS003 Refsum Disease, Infantile Form 27 0.573
599
PLY100 Polyploidy 36 0.573
600
STT009 Sutton Disease 2 30 0.573
601
TXC020 Toxic Oil Syndrome 33 0.573
602
GLM044 Glomerular Disease 34 0.573
603
RGH006 Right Aortic Arch 28 0.573
604
NNT021 Neonatal Meningitis 22 0.573
605
SPC030 Specific Language Disorder 25 0.573
606
APL002 Aplasia of Lacrimal and Salivary Glands 55 0.571
607
PLY105 Polycystic Ovary Syndrome 1 39 0.571
608
P MJR001 Major Depressive Disorder 68 0.558
609
MNT002 Mental Depression 56 0.558
610
ALL006 Allergic Asthma 55 0.558
611
DPR016 Depression 64 0.558
612
MYL009 Myelodysplastic Syndrome 67 0.538
613
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.538
614
ATR057 Atrioventricular Block 54 0.538
615
c VSC019 Vesicoureteral Reflux 1 56 0.538
616
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 0.538
617
BTT016 Batten-Turner Congenital Myopathy 54 0.538
618
HNZ004 Heinz Body Anemias 40 0.538
619
c GLY016 Glycogen Storage Disease Ib 41 0.538
620
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 0.538
621
ANG020 Angiosarcoma 63 0.538
622
GDP001 Goodpasture Syndrome 54 0.538
623
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.538
624
PRS064 Persistent Vegetative State 33 0.538
625
CRT004 Carotid Artery Thrombosis 39 0.538
626
P KRN004 Kernicterus 47 0.538
627
NVS001 Neovascular Glaucoma 52 0.538
628
VSM001 Vasomotor Rhinitis 38 0.538
629
SGT001 Sagittal Sinus Thrombosis 36 0.538
630
BLN008 Blind Hypotensive Eye 15 0.538
631
BLD052 Blood Group Incompatibility 31 0.538
632
TNG007 Tongue Carcinoma 55 0.538
633
RGH001 Right Bundle Branch Block 47 0.538
634
HMN016 Hemangioendothelioma 35 0.538
635
NCR007 Necrotizing Fasciitis 48 0.538
636
INT104 Intravascular Papillary Endothelial Hyperplasia 30 0.538
637
ACT228 Acute Radiation Syndrome 30 0.538
638
RTF001 Retiform Hemangioendothelioma 17 0.538
639
URM005 Uremic Pruritus 46 0.538
640
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.538
641
ART140 Arteries, Anomalies of 52 0.535
642
P ATS364 Autism 72 0.535
643
LPP008 Lipoprotein Quantitative Trait Locus 65 0.535
644
FDL002 Food Allergy 47 0.535
645
P EPL164 Epilepsy 70 0.535
646
SVR001 Severe Acute Respiratory Syndrome 68 0.535
647
c HPT003 Hepatitis a 63 0.535
648
P RTN018 Retinal Disease 53 0.535
650
MYF002 Myofascial Pain Syndrome 46 0.530
651
GST009 Gastroschisis 53 0.508
652
c SPN225 Spondyloarthropathy 1 70 0.508
653
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.508
654
SPH010 Sphingolipidosis 47 0.508
655
BRN009 Burning Mouth Syndrome 51 0.508
656
CRH001 Crohn's Disease 80 0.508
657
CCN002 Cocaine Abuse 49 0.508
658
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.473
659
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.473
660
c PNS012 Paine Syndrome 60 0.473
661
P MYM013 Moyamoya Disease 1 59 0.473
662
PDC001 Podoconiosis 42 0.473
663
P FTL001 Fetal Alcohol Syndrome 55 0.473
664
CRB025 Carbohydrate Metabolic Disorder 41 0.473
665
ELP001 Elephantiasis 43 0.473
666
NRT001 Neurotic Disorder 56 0.473
667
DSS008 Disease of Mental Health 74 0.473
668
HMP005 Hemiplegia 53 0.473
669
P PRS038 Personality Disorder 65 0.473
670
P HMR005 Hemorrhoid 49 0.473
671
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 38 0.473
672
ARG004 Argyria 26 0.473
673
c PRG020 Paragangliomas 3 39 0.453
674
c NGH010 Night Blindness, Congenital Stationary, Autosomal Dominant 2 45 0.453
675
P HYP058 Hypervitaminosis a 47 0.453
676
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.453
677
P SDR002 Siderosis 42 0.453
678
SLD003 Sialadenitis 47 0.453
679
RHM028 Rheumatic Heart Disease 55 0.453
680
ART074 Aortic Dissection 53 0.453
681
OCL010 Ocular Hypotension 37 0.453
682
c ATM075 Autoimmune Encephalitis 39 0.453
683
CHR158 Charles Bonnet Syndrome 23 0.453
684
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.433
685
P MSC003 Muscular Atrophy 52 0.389
686
P INF038 Influenza 68 0.389
687
P PRV006 Pervasive Developmental Disorder 52 0.388
688
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.388
689
PSR001 Psoriatic Arthritis 61 0.388
690
CRH005 Crohn's Colitis 53 0.388
691
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.388
692
c PRM108 Primary Progressive Multiple Sclerosis 51 0.388
693
c PSR028 Psoriasis 7 42 0.388
694
CLS016 Clostridium Difficile Colitis 49 0.388
695
c PSR023 Psoriasis 1 52 0.388
696
P FNG006 Feingold Syndrome 1 61 0.388
697
P MJR007 Major Affective Disorder 1 42 0.388
698
c MCL046 Mucolipidosis Iii Alpha/beta 61 0.388
699
P NJM001 Nijmegen Breakage Syndrome 75 0.388
700
c MJR008 Major Affective Disorder 2 34 0.388
701
c INF071 Inflammatory Bowel Disease 1 65 0.388
702
c EXD008 Exudative Vitreoretinopathy 1 71 0.388
703
c PSR017 Psoriasis 2 53 0.388
704
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.388
705
P ALT001 Alternating Hemiplegia of Childhood 56 0.388
706
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.388
707
c MJR006 Major Affective Disorder 5 32 0.388
708
c MJR023 Major Affective Disorder 7 33 0.388
709
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 0.388
710
FTL006 Fetal Alcohol Spectrum Disorder 43 0.388
711
ANG049 Angioedema Induced by Ace Inhibitors 38 0.388
712
HYP781 Hypoascorbemia 52 0.388
713
P SJG008 Sjogren Syndrome 60 0.388
714
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.388
715
c PSR018 Psoriasis 13 40 0.388
716
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 0.388
717
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.388
718
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.388
719
P OCL013 Oculodentodigital Dysplasia 66 0.388
720
P CNR004 Cone-Rod Dystrophy 2 74 0.388
721
c PSR032 Psoriasis 11 47 0.388
722
KRT013 Keratolytic Winter Erythema 45 0.388
723
c FNC043 Fanconi Anemia, Complementation Group E 62 0.388
724
c HYP575 Hypotrichosis 7 45 0.388
725
c MJR004 Major Affective Disorder 4 28 0.388
726
c MJR003 Major Affective Disorder 6 32 0.388
727
END040 Endogenous Depression 54 0.388
728
NRG001 Neurogenic Bowel 31 0.388
729
VLV010 Vulvovaginitis 42 0.388
730
ANS012 Anus Disease 49 0.388
731
CNT017 Central Nervous System Origin Vertigo 44 0.388
732
NNT012 Neonatal Jaundice 53 0.388
733
ANL018 Analbuminemia 53 0.388
734
ATN011 Autoinflammation with Infantile Enterocolitis 46 0.388
735
P HYP087 Hypotrichosis 41 0.388
736
RDN001 Reading Disorder 40 0.388
737
PNT038 Peanut Allergy 45 0.388
738
CRB009 Cerebritis 43 0.388
739
VSL002 Visual Epilepsy 39 0.388
740
NSP002 Nasopharyngitis 45 0.388
741
VGN020 Vaginal Disease 49 0.388
742
FLR001 Filarial Elephantiasis 59 0.388
743
CHR066 Chronic Fatigue Syndrome 59 0.388
745
c PRM038 Primary Agammaglobulinemia 47 0.388
746
END072 Endotheliitis 36 0.388
747
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.388
748
RFR003 Refractive Error 41 0.388
749
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.388
750
P ALP009 Alopecia Areata 59 0.388
751
AND005 Androgen Insensitivity Syndrome, Mild 21 0.388
752
SWL001 Swallowing Disorders 37 0.388
753
RSP007 Respiratory Distress Syndrome, Infant 41 0.388
754
NCR014 Necrotizing Soft Tissue Infection 24 0.388
755
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.388
756
MST020 Mast Cell Activation Syndrome 27 0.388
757
FTL073 Fetal Anticonvulsant Syndrome 23 0.388
758
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.380
759
IMM167 Immune Deficiency Disease 76 0.370
760
P CND004 Candidiasis 57 0.370
761
P ANT006 Antiphospholipid Syndrome 55 0.370
762
ATM095 Autoimmune Disease 61 0.360
763
P TRM003 Tremor 50 0.360
764
ANR007 Anorexia Nervosa 59 0.350
765
c PRC016 Pre-Eclampsia 64 0.350
766
END086 End Stage Renal Disease 54 0.350
767
ETN001 Eating Disorder 59 0.350
768
c HPT073 Hepatitis C Virus 70 0.340
769
PRS045 Prostatic Hypertrophy 53 0.340
770
c MGR028 Migraine with or Without Aura 1 63 0.329
771
STT001 Status Epilepticus 58 0.329
772
P CMP008 Compartment Syndrome 49 0.318
773
ANP008 Anaplastic Oligoastrocytoma 31 0.318
774
P ENC004 Encephalitis 61 0.318
775
SPN186 Spinal Cord Injury 60 0.318
776
CHR100 Chronic Ulcer of Skin 57 0.306
777
P PLM037 Pulmonary Hypertension 69 0.306
778
RBS001 Rabies 57 0.306
779
c HPT001 Hepatitis C 61 0.306
780
P KRT007 Keratoconus 49 0.306
781
LPD009 Lipid Storage Disease 45 0.306
782
P ALZ034 Alzheimer Disease 87 0.294
783
HMC014 Homocysteinemia 52 0.294
784
DSS032 Disease by Infectious Agent 55 0.294
785
BRT005 Barth Syndrome 55 0.294
786
CHD004 Chudley-Mccullough Syndrome 47 0.294
787
FRC013 Fructose Utilization 15 0.294
788
DPH001 Diphtheria 59 0.294
789
PRS021 Prostatic Adenoma 43 0.294
790
PRT013 Portal Hypertension 59 0.294
791
P HML002 Hemolytic Anemia 62 0.294
792
ACT119 Acute Promyelocytic Leukemia 62 0.282
793
P LKM062 Leukemia, Acute Lymphoblastic 69 0.282
794
P DNG005 Dengue Virus 55 0.282
795
CLN015 Colon Adenocarcinoma 64 0.282
796
c CHR684 Chronic Kidney Disease 73 0.282
797
P PRD006 Prader-Willi Syndrome 60 0.268
798
PRS129 Prostatic Hyperplasia, Benign 48 0.268
799
THR024 Thrombosis 56 0.268
800
P MCR010 Microcephaly 59 0.268
801
P MYT002 Myotonic Dystrophy 51 0.268
802
P MLG056 Malignant Hyperthermia 65 0.268
803
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.255
804
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.255
805
VLV047 Volvulus of Midgut 55 0.255
806
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.255
807
P PRP019 Peripheral Nervous System Disease 57 0.255
808
P GLM007 Glomerulonephritis 59 0.255
809
P MYL006 Myeloid Leukemia 60 0.255
810
P TRC031 Trichorhinophalangeal Syndrome 37 0.255
811
P OVR082 Overgrowth Syndrome 41 0.255
812
INF034 Infective Endocarditis 53 0.240
813
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.240
814
c CNG012 Congenital Generalized Lipodystrophy 65 0.240
815
HYP020 Hyperprolactinemia 63 0.240
816
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.240
817
c OPT053 Optic Atrophy 1 62 0.240
818
P LNG028 Long Qt Syndrome 63 0.240
819
P PYL005 Pyelonephritis 56 0.240
820
P LTR001 Lateral Sclerosis 57 0.240
821
ACT098 Acute Erythroid Leukemia 55 0.240
822
P END033 Endocarditis 58 0.240
823
MTH009 Mouth Disease 57 0.240
824
P UVT001 Uveitis 57 0.240
825
SCH014 Schistosomiasis 56 0.240
826
P URT039 Urticaria 57 0.240
827
P LPS004 Lupus Erythematosus 61 0.240
828
PRN019 Perinatal Necrotizing Enterocolitis 60 0.240
829
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.240
830
c LKM005 Leukemia, T-Cell, Chronic 33 0.240
831
CYN003 Cyanide Poisoning 22 0.240
832
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.225
833
c SYS001 Systemic Lupus Erythematosus 85 0.225
834
P OST002 Osteoporosis 76 0.225
835
AST006 Astigmatism 46 0.225
836
c MCR133 Microvascular Complications of Diabetes 4 41 0.225
837
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.225
838
c MCR113 Microvascular Complications of Diabetes 3 52 0.225
839
c MCR130 Microvascular Complications of Diabetes 6 41 0.225
840
c MCR120 Microvascular Complications of Diabetes 7 47 0.225
841
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.225
842
PHN003 Phenylketonuria 76 0.225
843
c LKM063 Leukemia, Chronic Myeloid 70 0.225
844
MLT157 Multiple System Atrophy 1 69 0.225
845
P PHC003 Pheochromocytoma 70 0.225
846
BCT021 Bacterial Sepsis 43 0.225
847
ADR040 Adrenal Gland Pheochromocytoma 45 0.225
848
ERY004 Erysipelas 47 0.225
849
P NPH012 Nephrotic Syndrome 61 0.225
850
BLL004 Bullous Keratopathy 48 0.225
851
P HYP069 Hyperparathyroidism 62 0.225
852
P LKM002 Leukemia 65 0.225
853
KRT008 Keratopathy 46 0.225
854
DNT012 Dental Caries 53 0.225
855
SKN022 Skin Squamous Cell Carcinoma 53 0.225
856
ACR007 Acromegaly 70 0.225
857
RNL001 Renal Artery Obstruction 31 0.225
858
PPL022 Papilloma 53 0.225
859
HYP014 Hyperuricemia 51 0.225
860
PRP016 Paraplegia 52 0.225
861
P MYP006 Myopia 55 0.225
862
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.225
863
SQM002 Squamous Cell Papilloma 45 0.225
864
P END044 Endometriosis 62 0.225
865
c HPT016 Hepatitis B 62 0.225
866
c SCN007 Secondary Hyperparathyroidism 50 0.225
867
ECH003 Echinococcosis 52 0.225
868
P DMN002 Dementia 65 0.225
869
PLR008 Pleurisy 49 0.225
870
GST050 Gastrointestinal System Disease 55 0.225
871
PRT058 Pure Autonomic Failure 58 0.225
872
P OVR042 Ovarian Cancer 88 0.208
873
P KRB001 Krabbe Disease 69 0.208
874
ACT088 Acute Insulin Response 39 0.208
875
RST023 Resting Heart Rate, Variation in 40 0.208
876
ANX010 Anxiety 70 0.208
877
CYN002 Cyanosis, Transient Neonatal 43 0.208
878
c GLL024 Gallbladder Disease 1 53 0.208
879
MLD001 Melioidosis 67 0.208
880
ACN002 Acanthosis Nigricans 56 0.208
881
c HYP739 Hyperlipoproteinemia, Type Iv 53 0.208
882
c HYP740 Hyperlipoproteinemia, Type V 54 0.208
883
GST023 Gastric Ulcer 52 0.208
884
PST028 Post-Traumatic Stress Disorder 58 0.208
885
P LPS002 Liposarcoma 64 0.208
886
EXC002 Exocrine Pancreatic Insufficiency 42 0.208
887
P ECL001 Eclampsia 52 0.208
888
P URN019 Urinary Tract Infection 48 0.208
889
P PLY019 Polyneuropathy 52 0.208
890
P ADN016 Adenocarcinoma 63 0.208
891
AVN001 Avian Influenza 61 0.208
892
PLC005 Placental Insufficiency 55 0.208
893
TRT001 Teratocarcinoma 41 0.208
894
P HYP061 Hypertrophic Cardiomyopathy 68 0.208
895
ORL005 Oral Candidiasis 55 0.208
896
P HML001 Hemolytic-Uremic Syndrome 52 0.208
897
SCR011 Scrapie 39 0.208
898
P HYP083 Hypopituitarism 51 0.208
899
CHL045 Choline Deficiency Disease 39 0.208
900
MSL001 Measles 61 0.208
901
NRM001 Neuromyelitis Optica 60 0.208
902
GNT167 Genetic Obesity 33 0.208
903
c PRM340 Primary Adrenal Insufficiency 37 0.208
904
P GLL020 Gallbladder Disease 57 0.190
905
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.190
906
PHS025 Phosphatase, Acid, of Tissues 28 0.190
907
CRD132 Cardiac Conduction Defect 59 0.190
908
RTC009 Reticulum Cell Sarcoma 43 0.190
909
P CLR023 Colorectal Cancer 100 0.190
911
DSM002 Desmosterolosis 39 0.190
912
RST011 Restrictive Dermopathy, Lethal 51 0.190
913
PRP027 Peripheral Vascular Disease 71 0.190
914
MJD001 Majeed Syndrome 39 0.190
915
c DVL110 Developmental and Epileptic Encephalopathy 88 21 0.190
916
P FRG001 Fragile X Syndrome 70 0.190
917
c ATR087 Atrial Standstill 1 74 0.190
918
ESP021 Esophageal Cancer 84 0.190
919
END057 Endometrial Cancer 76 0.190
920
CHR005 Chorioamnionitis 50 0.190
921
OST017 Osteomyelitis 63 0.190
922
PRS025 Presbyopia 39 0.190
923
P EPD016 Epidermolysis Bullosa 53 0.190
924
P CNJ013 Conjunctivitis 66 0.190
925
RTC003 Root Caries 33 0.190
926
CRN009 Corneal Ectasia 30 0.190
927
DMY004 Demyelinating Disease 50 0.190
928
PLS011 Plasmacytoma 56 0.190
929
P LKD001 Leukodystrophy 58 0.190
930
PLR001 Pleural Tuberculosis 49 0.190
931
LPR001 Lepromatous Leprosy 49 0.190
932
PLS007 Plasmodium Falciparum Malaria 52 0.190
933
OBS004 Obstructive Hydrocephalus 44 0.190
934
RTC005 Reticulosarcoma 47 0.190
935
P CHL066 Cholangitis 51 0.190
936
CHC001 Chickenpox 56 0.190
937
P AMY004 Amyloidosis 69 0.190
938
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 0.190
939
GRW007 Growth Hormone Deficiency 47 0.190
940
P SCH015 Schizophrenia 74 0.170
941
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.170
942
LPM012 Lipomatosis, Multiple 59 0.170
943
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.170
944
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 0.170
945
P PRP003 Porphyria Cutanea Tarda 66 0.170
946
FCS014 Fucosidase Regulator 15 0.170
947
ABT001 Abetalipoproteinemia 68 0.170
948
P CHN012 Chondrosarcoma 56 0.170
949
c HMC039 Hemochromatosis, Type 1 73 0.170
950
MND023 Mend Syndrome 49 0.170
951
P STR020 Strabismus 56 0.170
952
PLY052 Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract 42 0.170
953
P MLN069 Melanoma, Uveal 59 0.170