Search results for Methionine

2451 hits were found for Methionine

# Family MCID Name MIFTS Score
1
HYP003 Hypermethioninemia 51 37.736
2
MTH074 Methionine Adenosyltransferase I/iii Deficiency 42 35.587
3
HMC033 Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type 34 24.761
4
HMC014 Homocysteinemia 52 22.617
5
MTH011 Methionine Adenosyltransferase Deficiency 18 20.085
6
P HMC002 Homocystinuria 53 16.621
7
NNL005 Non-Alcoholic Fatty Liver Disease 63 16.107
8
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 33 14.436
9
FTT001 Fatty Liver Disease 62 14.407
10
NNL006 Non-Alcoholic Steatohepatitis 54 14.099
11
MTH075 Methionine Malabsorption Syndrome 14 14.058
12
GLY015 Glycine N-Methyltransferase Deficiency 40 13.964
13
GLL048 Glial Tumor 52 11.920
14
GLM045 Glioma 63 11.844
15
MTH046 Methylmalonic Acidemia Without Homocystinuria 39 11.507
16
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 38 11.310
17
ALP077 Alpha-Methylacetoacetic Aciduria 52 11.181
18
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 10.591
19
MTH021 Methylmalonic Acidemia with Homocystinuria 44 10.212
20
P VSC007 Vascular Disease 63 9.635
21
P LVR013 Liver Disease 69 9.602
22
NRL016 Neural Tube Defects 81 9.572
23
DSR079 Disorder of Methionine Cycle and Sulfur Amino Acid Metabolism 4 9.357
24
GLB002 Glioblastoma 67 9.084
25
RPD005 Rapidly Involuting Congenital Hemangioma 46 9.032
26
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 8.315
27
P GLM040 Glioma Susceptibility 1 71 7.866
28
VTM002 Vitamin B12 Deficiency 48 7.778
29
CHL068 Cholestasis 61 7.729
30
ADN018 Adenoma 59 7.430
31
CRT072 Creutzfeldt-Jakob Disease 68 7.227
32
HLX001 Helix Syndrome 48 7.131
33
P NRB001 Neuroblastoma 66 6.934
34
LVR012 Liver Cirrhosis 63 6.931
35
P HYP069 Hyperparathyroidism 62 6.927
36
HGH043 High Grade Glioma 45 6.763
37
MNT002 Mental Depression 57 6.730
38
DPR016 Depression 65 6.650
39
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 6.549
40
CHL045 Choline Deficiency Disease 39 6.484
41
P ENC018 Encephalopathy 62 6.425
42
P PRN023 Prion Disease 60 6.389
43
P MJR001 Major Depressive Disorder 68 6.339
44
DWN001 Down Syndrome 70 6.335
45
c INH020 Inherited Metabolic Disorder 48 6.287
46
MLG169 Malignant Astrocytoma 57 6.186
47
P HPT023 Hepatocellular Carcinoma 96 6.070
48
MGL001 Megaloblastic Anemia 58 5.793
49
ATH013 Atherosclerosis Susceptibility 63 5.769
50
P HPT021 Hepatitis 69 5.741
51
AGN016 Aging 54 5.731
52
48X005 48,xyyy 39 5.643
53
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 5.560
54
HPT004 Hepatic Coma 43 5.527
55
INS024 Insulin-Like Growth Factor I 78 5.499
56
MYL069 Myeloma, Multiple 77 5.490
57
c PRM005 Primary Hyperparathyroidism 59 5.377
58
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 5.313
59
HPT019 Hepatic Encephalopathy 59 5.226
60
c HPT001 Hepatitis C 62 5.218
61
P MDL005 Medulloblastoma 75 5.130
62
P MTH008 Methylmalonic Acidemia 52 5.013
63
P PRS040 Prostate Cancer 95 4.966
64
P ALZ034 Alzheimer Disease 87 4.907
65
DSR002 Disorders of Intracellular Cobalamin Metabolism 29 4.887
66
P LYM118 Lymphoma 67 4.751
67
HMN044 Human Immunodeficiency Virus Type 1 78 4.622
68
c HPT016 Hepatitis B 62 4.620
69
PPL052 Papillomatosis, Confluent and Reticulated 34 4.577
70
LPP008 Lipoprotein Quantitative Trait Locus 65 4.547
71
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.544
72
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.526
73
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.526
74
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.526
75
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.526
76
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.526
77
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.526
78
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.526
79
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.526
80
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.526
81
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.526
82
MNN043 Meningioma, Familial 79 4.502
83
SCR001 Secretory Meningioma 40 4.502
84
LYM002 Lymphoplasmacyte-Rich Meningioma 35 4.502
85
SPN021 Spinal Meningioma 50 4.502
86
ACQ007 Acquired Immunodeficiency Syndrome 59 4.459
87
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 4.459
88
OST159 Osteogenic Sarcoma 66 4.427
89
P LKM062 Leukemia, Acute Lymphoblastic 69 4.400
90
P URN019 Urinary Tract Infection 49 4.379
91
P PNC035 Pancreatic Cancer 86 4.346
92
P ALC033 Alcohol Use Disorder 61 4.346
93
P AMY004 Amyloidosis 70 4.327
94
c PCH010 Pachyonychia Congenita 3 43 4.294
95
PRM236 Primary Biliary Cholangitis 60 4.293
96
P OLG002 Oligodendroglioma 66 4.264
97
P CRD246 Cardiovascular System Disease 56 4.264
98
P MYP004 Myopathy 67 4.250
99
c HYP836 Hypercholesterolemia, Familial, 1 73 4.234
100
P PHC003 Pheochromocytoma 69 4.230
101
LWG006 Low Grade Glioma 41 4.212
102
ADR040 Adrenal Gland Pheochromocytoma 46 4.195
103
P HRP006 Herpes Simplex 65 4.168
104
SRC014 Sarcoma 65 4.165
105
ALC007 Alcohol Dependence 66 4.155
106
SPN035 Spindle Cell Sarcoma 54 4.136
107
c PRC016 Pre-Eclampsia 65 4.124
108
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 4.121
109
ART140 Arteries, Anomalies of 53 4.115
110
P RHB003 Rhabdomyosarcoma 66 4.100
111
P PLY019 Polyneuropathy 52 4.085
112
c CHR684 Chronic Kidney Disease 69 4.079
113
47X002 47,xyy 48 4.055
114
PRT029 Parathyroid Adenoma 51 4.022
115
P ATS364 Autism 69 4.011
116
P BCL017 B-Cell Lymphoma 59 3.980
117
P PNC044 Pancreatitis 61 3.936
118
P FTL002 Fatal Familial Insomnia 50 3.930
119
P SZR006 Seizure Disorder 70 3.917
120
P HML002 Hemolytic Anemia 62 3.898
121
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 34 3.897
122
VSC002 Vascular Dementia 60 3.891
123
DFC004 Deficiency Anemia 74 3.880
124
P HYP265 Hypotonia 42 3.864
125
c BRN108 Branchiootic Syndrome 1 62 3.829
126
P HRT032 Heart Disease 81 3.828
127
P DMN002 Dementia 66 3.826
128
STM007 Stomatitis 54 3.826
129
P PTT006 Pituitary Adenoma 55 3.825
130
CYS001 Cystic Fibrosis 78 3.798
131
P SCH015 Schizophrenia 74 3.786
132
THY029 Thyroid Carcinoma 51 3.784
133
P ART021 Arteriosclerosis 54 3.784
134
P BRS047 Breast Cancer 98 3.775
135
c ACT068 Acute Cystitis 61 3.770
136
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 34 3.764
137
VCC001 Vaccinia 47 3.730
138
CRB039 Cerebrovascular Disease 66 3.714
139
HRN029 Hearing Loss, Noise-Induced 37 3.700
140
P BPL003 Bipolar Disorder 56 3.689
141
PYR009 Pyridoxine Deficiency Anemia 35 3.683
142
THR024 Thrombosis 56 3.678
143
P LTR001 Lateral Sclerosis 58 3.670
144
END086 End Stage Renal Disease 52 3.645
145
c MJR022 Major Affective Disorder 8 38 3.642
146
c MJR024 Major Affective Disorder 9 41 3.642
147
ANP005 Anaplastic Astrocytoma 57 3.640
148
c AMY091 Amyotrophic Lateral Sclerosis 1 88 3.628
149
END040 Endogenous Depression 55 3.598
150
HYP060 Hyperinsulinism 54 3.598
151
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 56 3.594
152
HYP066 Hyperglycemia 61 3.570
153
ATS010 Autosomal Recessive Disease 42 3.568
154
c HPT003 Hepatitis a 63 3.537
155
ARG004 Argyria 26 3.535
156
LPD008 Lipid Metabolism Disorder 62 3.532
157
CLL010 Cellular Ependymoma 57 3.491
158
P BNG030 Benign Ependymoma 51 3.491
159
P MYC084 Mycobacterium Tuberculosis 1 68 3.477
160
EWN003 Ewing Sarcoma 70 3.470
161
P INF032 Infertility 57 3.461
162
P KDN018 Kidney Disease 72 3.460
163
ALC006 Alcoholic Hepatitis 61 3.452
164
P EPL164 Epilepsy 68 3.443
165
MTB004 Metabolic Acidosis 48 3.434
166
c TYP009 Type 2 Diabetes Mellitus 92 3.402
167
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.390
168
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 3.377
169
CHL014 Cholera 62 3.362
170
PTT037 Pituitary Tumors 44 3.360
171
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.340
172
PRC051 Paracetamol Poisoning 29 3.316
173
P SRC025 Sarcoidosis 1 71 3.305
174
BRN028 Brain Cancer 74 3.299
175
P LNG032 Lung Cancer 98 3.298
176
NWC001 Newcastle Disease 47 3.289
177
CYT002 Cytokine Deficiency 43 3.283
178
P CRN300 Coronary Heart Disease 1 73 3.280
179
HYP266 Hypoxia 57 3.272
180
CYS019 Cystathioninuria 46 3.257
181
P RTN024 Retinoblastoma 73 3.252
182
P RCT021 Rectum Cancer 54 3.246
183
PRT037 Pertussis 65 3.239
184
SFT003 Soft Tissue Sarcoma 57 3.231
185
NRT001 Neurotic Disorder 56 3.226
186
P GST053 Gastric Cancer 83 3.224
187
c HYP595 Hypertension, Essential 85 3.219
188
IMM167 Immune Deficiency Disease 78 3.216
189
P CLR023 Colorectal Cancer 100 3.215
190
CRC021 Carcinosarcoma 64 3.202
191
PRP027 Peripheral Vascular Disease 71 3.198
192
IRN002 Iron Metabolism Disease 57 3.186
193
ADL002 Adult Syndrome 70 3.164
194
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.153
195
CRH001 Crohn's Disease 80 3.151
196
CRN036 Craniopharyngioma 64 3.145
197
CLR108 Colorectal Adenoma 64 3.128
198
P NRP001 Neuropathy 60 3.123
199
c THR092 Thrombophilia Due to Thrombin Defect 74 3.105
200
BCT022 Bacterial Infectious Disease 56 3.097
201
P ADN016 Adenocarcinoma 63 3.091
202
LYM019 Lymphosarcoma 46 3.079
203
P HYP086 Hypothyroidism 69 3.077
204
CLF027 Cleft Palate, Isolated 64 3.069
205
BRN004 Brain Edema 54 3.060
206
PHN003 Phenylketonuria 76 3.056
207
HYP056 Hypoglycemia 65 3.048
208
P PRK057 Parkinson Disease, Late-Onset 80 3.048
209
MLD018 Mild Cognitive Impairment 48 3.033
210
ATM095 Autoimmune Disease 61 3.016
211
c TYP008 Type 1 Diabetes Mellitus 70 3.015
212
P MLT020 Multiple Sclerosis 79 3.013
213
NRL018 Neural Tube Defects, Folate-Sensitive 45 3.010
214
DPH001 Diphtheria 59 2.994
215
P CTR002 Cataract 60 2.990
216
P CNT005 Central Nervous System Lymphoma 52 2.984
217
PRM226 Primary Central Nervous System Lymphoma 47 2.984
218
PNG002 Pain Agnosia 51 2.966
219
c ACT134 Acute Liver Failure 59 2.961
220
OCL069 Ocular Motor Apraxia 57 2.909
221
P OVR042 Ovarian Cancer 88 2.887
222
P LKM002 Leukemia 67 2.887
223
HRW001 Hair Whorl 35 2.885
224
ISL099 Isolated Methylmalonic Acidemia 36 2.885
225
SCR011 Scrapie 39 2.870
226
ISC004 Ischemia 61 2.870
227
P TYR004 Tyrosinemia 50 2.865
228
PLC008 Placenta Disease 49 2.864
229
P MLN008 Melanoma 76 2.862
230
ANX010 Anxiety 70 2.855
231
HMP009 Haemophilus Influenzae 41 2.846
232
P OBS001 Obstructive Jaundice 48 2.839
233
LYM143 Lymphoma, Non-Hodgkin, Familial 75 2.836
234
P MSC005 Muscular Dystrophy 67 2.836
235
P BNG032 Benign Mesothelioma 53 2.834
236
ANX004 Anoxia 40 2.822
237
c HPT073 Hepatitis C Virus 71 2.822
238
P KLZ004 Kala-Azar 1 41 2.808
239
LSH001 Leishmaniasis 64 2.808
240
P MYC033 Myoclonus 47 2.806
241
THY111 Thyroid Carcinoma, Familial Medullary 67 2.777
242
c ACT027 Acute Pancreatitis 60 2.759
243
THY125 Thyroid Gland Medullary Carcinoma 48 2.756
244
P HYP750 Hypertriglyceridemia, Familial 62 2.756
245
HMS001 Hemosiderosis 48 2.749
246
LNG099 Lung Disease 62 2.746
247
P MLN007 Male Infertility 56 2.734
248
P MCR010 Microcephaly 60 2.733
249
KR002 Kuru 45 2.710
250
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.709
251
CLT003 Colitis 63 2.678
252
P HNT016 Huntington Disease 73 2.678
253
P TRM003 Tremor 48 2.673
254
STR067 Stroke, Ischemic 80 2.647
255
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.645
256
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 2.641
257
LYM133 Lymphoma, Hodgkin, Classic 74 2.621
258
c MGR028 Migraine with or Without Aura 1 64 2.619
259
ALL014 Allergic Encephalomyelitis 34 2.597
260
ULC004 Ulcerative Colitis 74 2.594
261
P BLD134 Bladder Cancer 79 2.577
262
P FBR017 Fibrosarcoma 56 2.569
263
URL001 Urolithiasis 46 2.568
264
CCC002 Coccidiosis 50 2.568
265
P CHR012 Chronic Granulomatous Disease 69 2.558
266
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 35 2.554
267
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.546
268
c ATS007 Autism Spectrum Disorder 72 2.535
269
P INF037 Inflammatory Bowel Disease 53 2.519
270
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.510
271
c LKM005 Leukemia, T-Cell, Chronic 34 2.510
272
DFF005 Diffuse Large B-Cell Lymphoma 54 2.509
273
NTR005 Nutritional Deficiency Disease 61 2.506
274
P DBT009 Diabetes Mellitus 67 2.500
275
P RHM011 Rheumatoid Arthritis 82 2.498
276
CHL065 Cholangiocarcinoma 58 2.495
277
INT079 Intrahepatic Cholangiocarcinoma 51 2.495
278
SVR004 Severe Combined Immunodeficiency 72 2.494
279
LWG005 Low-Grade Astrocytoma 38 2.478
280
P ISL078 Isolated Ectopia Lentis 58 2.474
281
AMN006 Aminoaciduria 37 2.468
282
PYR016 Pyridoxine Deficiency 29 2.455
283
MCS002 Mucositis 56 2.452
284
WLS001 Wilson Disease 70 2.442
285
P PRK039 Parkinsonism 55 2.442
286
FBR047 Fibromyalgia 58 2.424
287
P ENC004 Encephalitis 61 2.415
288
SLP001 Sleeping Sickness 56 2.415
289
GLC003 Glucose Intolerance 54 2.388
290
PLS011 Plasmacytoma 56 2.385
291
P PLM036 Pulmonary Fibrosis 66 2.383
292
ACT098 Acute Erythroid Leukemia 55 2.366
294
TRY001 Trypanosomiasis 50 2.364
295
P ECL001 Eclampsia 52 2.364
296
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.361
297
PRT251 Proteinuria, Chronic Benign 57 2.361
298
BNR002 Bone Resorption Disease 47 2.361
299
PTH003 Pathologic Nystagmus 52 2.356
300
P PRP019 Peripheral Nervous System Disease 58 2.343
301
CRV035 Cervical Cancer 73 2.329
302
P INT099 Intrahepatic Cholestasis of Pregnancy 62 2.315
303
P TMP001 Temporal Lobe Epilepsy 49 2.315
304
MLG079 Malignant Pleural Mesothelioma 42 2.315
305
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.312
306
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.312
307
URM002 Uremia 47 2.312
308
P DNG005 Dengue Virus 56 2.312
309
P MYC007 Myocardial Infarction 70 2.305
310
FLT009 Folate Malabsorption, Hereditary 49 2.298
311
P CRB088 Cerebral Atrophy 33 2.286
312
CHR074 Choriocarcinoma 46 2.271
313
P PLM006 Pulmonary Alveolar Proteinosis 53 2.269
314
CHL123 Chlamydia 58 2.259
315
P MYS005 Myositis 56 2.248
316
KWS001 Kwashiorkor 45 2.247
317
ACR007 Acromegaly 70 2.244
318
TBC004 Tobacco Addiction 63 2.234
319
P INF038 Influenza 68 2.233
320
MST005 Mastitis 53 2.232
321
CLF001 Cleft Lip 53 2.232
322
OST012 Osteoarthritis 77 2.230
323
P MLT074 Multiple Endocrine Neoplasia 59 2.221
325
CYS013 Cystinuria 66 2.209
326
P ART022 Arthritis 71 2.204
327
c DLT002 Dilated Cardiomyopathy 78 2.204
328
PLY150 Polykaryocytosis Inducer 29 2.186
329
c ACT071 Acute Kidney Failure 60 2.186
330
END057 Endometrial Cancer 72 2.175
331
P HDC001 Headache 57 2.167
332
c SCN007 Secondary Hyperparathyroidism 51 2.166
333
BRN024 Bronchitis 67 2.166
334
PRN011 Pernicious Anemia 53 2.157
335
BRK010 Burkitt Lymphoma 66 2.155
336
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 2.155
337
P HYP076 Hyperthyroidism 53 2.155
338
P BRS044 Breast Adenocarcinoma 58 2.147
339
P MPL001 Maple Syrup Urine Disease 70 2.144
340
OLG006 Oligoastrocytoma 34 2.129
341
P OVR082 Overgrowth Syndrome 49 2.123
342
SQM006 Squamous Cell Carcinoma 60 2.122
343
P THR015 Thrombophilia 51 2.117
344
TTN003 Tetanus 65 2.091
345
GTR002 Goiter 53 2.087
346
MXD026 Mixed Glioma 45 2.067
347
DFF016 Diffuse Astrocytoma 45 2.061
348
DYS006 Dysembryoplastic Neuroepithelial Tumor 32 2.061
349
GLM004 Gliomatosis Cerebri 52 2.061
350
P ATT013 Attention Deficit-Hyperactivity Disorder 64 2.057
351
P LNG064 Lung Cancer Susceptibility 3 70 2.057
352
P KDN017 Kidney Cancer 61 2.057
353
PPL022 Papilloma 53 2.042
354
MSL001 Measles 61 2.035
355
ANP009 Anaplastic Oligodendroglioma 41 2.026
356
STT001 Status Epilepticus 59 2.024
357
ESP021 Esophageal Cancer 83 2.023
358
c ACT075 Acute Myocardial Infarction 56 2.023
359
P MYC008 Myocarditis 59 2.023
360
ANP008 Anaplastic Oligoastrocytoma 29 2.001
361
c SCL052 Scleroderma, Familial Progressive 61 1.994
362
c TYR012 Tyrosinemia, Type I 61 1.994
363
TRM010 Traumatic Brain Injury 51 1.994
364
BRN071 Brain Injury 50 1.994
365
P MTR014 Motor Neuron Disease 65 1.991
366
MLR004 Malaria 80 1.988
367
GRM004 Germinoma 44 1.984
368
P MJR007 Major Affective Disorder 1 42 1.976
369
BRN032 Brain Glioma 45 1.968
370
SVR001 Severe Acute Respiratory Syndrome 67 1.961
371
P THL005 Thalassemia 56 1.952
372
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.952
373
PRP001 Propionic Acidemia 65 1.952
374
GNG004 Ganglioglioma 53 1.952
375
SCH014 Schistosomiasis 56 1.952
376
ALL029 Allergic Disease 59 1.951
377
c VRL010 Viral Hepatitis 53 1.949
378
MDD011 Mood Disorder 62 1.949
379
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.946
380
P PSR002 Psoriasis 63 1.946
381
PST011 Pustulosis of Palm and Sole 52 1.946
382
SQM002 Squamous Cell Papilloma 46 1.946
383
PLG002 Plague 58 1.946
384
P GLM007 Glomerulonephritis 60 1.946
385
P FLL037 Follicular Lymphoma 74 1.945
386
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 1.932
387
P RTN016 Retinal Degeneration 52 1.928
388
P PRD008 Periodontitis 64 1.928
389
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 1.919
390
INS001 Insulinoma 59 1.919
391
ADR022 Adrenomyeloneuropathy 39 1.915
392
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.915
393
ADR007 Adrenoleukodystrophy 73 1.915
394
P PLM037 Pulmonary Hypertension 72 1.915
395
NRR001 Neuroretinitis 42 1.915
396
RTN023 Retinitis 46 1.915
397
PNC129 Pancreatic Adenocarcinoma 65 1.915
398
ART016 Aortic Aneurysm 68 1.915
399
DSS032 Disease by Infectious Agent 55 1.904
400
ANR040 Aneurysm 61 1.904
401
AMN012 Aminoacidopathies 20 1.904
402
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.896
403
HYP141 Hyperphenylalaninemia 42 1.888
404
P RTN008 Retinitis Pigmentosa 80 1.876
405
FCL014 Focal Epilepsy 53 1.876
406
P CYS018 Cystitis 59 1.862
407
P PRP029 Porphyria 60 1.862
408
P OST002 Osteoporosis 76 1.858
409
CLF056 Cleft Lip with or Without Cleft Palate 42 1.858
410
PLM031 Poliomyelitis 63 1.858
411
PLC007 Placental Abruption 47 1.858
412
CHR178 Chromosomal Triplication 34 1.857
413
EXN003 Exencephaly 30 1.857
414
SKN016 Skin Disease 63 1.836
415
P PLY011 Polycystic Ovary Syndrome 57 1.836
416
CYS009 Cystadenoma 43 1.828
417
c MCR130 Microvascular Complications of Diabetes 6 41 1.825
418
c MCR120 Microvascular Complications of Diabetes 7 47 1.825
419
P SPP010 Suppressor of Tumorigenicity 3 51 1.825
420
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.825
421
P LPS004 Lupus Erythematosus 61 1.825
422
c MCR113 Microvascular Complications of Diabetes 3 52 1.825
423
c MCR133 Microvascular Complications of Diabetes 4 41 1.825
424
P MSC003 Muscular Atrophy 52 1.823
425
PRT010 Parathyroid Carcinoma 68 1.822
426
P VNW001 Von Willebrand's Disease 65 1.822
427
P RRH023 Rare Hereditary Hemochromatosis 54 1.822
428
BRN034 Brain Meningioma 33 1.817
429
INT395 Intracranial Meningioma 39 1.817
430
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 28 1.813
431
MCR025 Microhydranencephaly 33 1.795
432
c MCR115 Microvascular Complications of Diabetes 5 65 1.792
433
c HRD039 Hereditary Amyloidosis 45 1.792
434
PRS047 Prostatitis 58 1.785
435
ANN002 Anencephaly 57 1.785
436
P SML001 Small Cell Carcinoma 52 1.785
437
c HNT010 Huntington Disease-Like 1 55 1.785
438
P ADL010 Adult Respiratory Distress Syndrome 71 1.785
439
KRT002 Keratomalacia 55 1.776
440
TRN015 Transient Cerebral Ischemia 63 1.770
441
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.766
442
c SML038 Small Cell Cancer of the Lung 69 1.759
443
P HML001 Hemolytic-Uremic Syndrome 52 1.759
444
CHC001 Chickenpox 57 1.759
445
HPT022 Hepatoblastoma 54 1.759
446
P GST044 Gastritis 55 1.759
447
OST017 Osteomyelitis 63 1.753
448
CRV002 Cervix Uteri Carcinoma in Situ 47 1.753
449
P SYP003 Syphilis 59 1.753
450
CRV045 Cervical Intraepithelial Neoplasia 39 1.753
451
PRT013 Portal Hypertension 59 1.747
452
GST045 Gastroenteritis 58 1.747
453
DMY004 Demyelinating Disease 50 1.747
454
c SYS001 Systemic Lupus Erythematosus 87 1.737
455
P CNR004 Cone-Rod Dystrophy 2 74 1.716
456
P PLV020 Pelvic Organ Prolapse 58 1.716
457
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.708
458
GST033 Gestational Diabetes 61 1.708
459
P DBT005 Diabetes Insipidus 54 1.707
460
c THY107 Thymoma, Familial 42 1.707
462
P THY023 Thymoma 64 1.707
463
c FML021 Familial Hypercholesterolemia 72 1.707
464
P RTN022 Retinal Vein Occlusion 54 1.707
465
P MTC069 Mitochondrial Disorders 57 1.695
466
c LKM056 Leukemia, Chronic Lymphocytic 2 48 1.690
467
CRD132 Cardiac Conduction Defect 60 1.690
468
c ATR087 Atrial Standstill 1 74 1.690
469
P GRV001 Graves' Disease 55 1.690
470
P HMN010 Hemangioma 62 1.690
471
CHR028 Chronic Wasting Disease 33 1.690
472
P NRF002 Neurofibromatosis 57 1.690
473
ATN005 Autonomic Dysfunction 46 1.690
474
MCR020 Microsporidiosis 49 1.670
475
HGH041 High-Grade Astrocytoma 36 1.670
476
ANR007 Anorexia Nervosa 60 1.666
477
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.666
478
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.666
479
P ALP008 Alopecia 54 1.666
480
TRN018 Transitional Cell Carcinoma 56 1.661
481
MCR017 Macrocytic Anemia 44 1.661
482
SPS057 Spasticity 42 1.654
483
c LKM061 Leukemia, Acute Myeloid 83 1.654
484
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 1.654
485
P DYS154 Dystonia 64 1.654
486
P LCT001 Lactic Acidosis 51 1.654
487
P DRR001 Diarrhea 55 1.654
488
HYP264 Hypertonia 36 1.654
489
P ANR048 Aniridia 1 64 1.630
490
AMD002 Amed Syndrome, Digenic 37 1.630
491
GRW007 Growth Hormone Deficiency 46 1.623
492
MDD018 Middle East Respiratory Syndrome 44 1.623
493
P SYS005 Systemic Scleroderma 74 1.623
495
c GLL024 Gallbladder Disease 1 52 1.616
496
P CHL066 Cholangitis 52 1.614
497
CYS010 Cystinosis 62 1.614
498
DRM006 Dermatitis 62 1.612
499
P BLR024 Biliary Cirrhosis, Primary, 1 28 1.612
500
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 35 1.612
501
MLD017 Mal De Debarquement Syndrome 29 1.612
502
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.587
503
CRB004 Cerebral Artery Occlusion 45 1.579
504
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.578
505
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.578
506
MTH071 Methane Production 25 1.578
507
LGH007 Leigh Syndrome 70 1.578
508
WST005 West Nile Virus 57 1.578
509
CNS004 Constipation 56 1.578
510
TXC005 Toxic Shock Syndrome 62 1.578
511
c RNG015 Ring Chromosome 2 22 1.578
512
AKN002 Akinetic Mutism 36 1.571
513
MTS001 Mutism 44 1.571
514
PPT005 Peptic Ulcer Disease 58 1.560
515
IMP005 Impotence 52 1.541
516
CNN005 Connective Tissue Disease 67 1.538
517
RCK004 Rickets 68 1.538
518
CYS005 Cysticercosis 60 1.538
519
CNG034 Congestive Heart Failure 69 1.538
520
P TCD001 Tic Disorder 49 1.538
521
NRM004 Neuroma 49 1.538
522
PLM012 Pulmonary Sarcoidosis 53 1.533
523
CRH005 Crohn's Colitis 53 1.532
524
P SNS001 Sensorineural Hearing Loss 59 1.532
525
HMG005 Hemoglobinopathy 56 1.532
526
P HYP024 Hypoparathyroidism 55 1.532
527
SPL018 Splenomegaly 49 1.532
528
P CHR345 Chronic Pain 50 1.532
529
P RSP003 Respiratory Failure 74 1.511
530
P ADL017 Adult T-Cell Leukemia 56 1.497
531
c ATM022 Autoimmune Myocarditis 36 1.497
532
P CND004 Candidiasis 58 1.497
533
PSY004 Psychotic Disorder 66 1.497
534
GST023 Gastric Ulcer 52 1.491
535
c HNT004 Huntington Disease-Like 2 52 1.483
536
P END046 Endometritis 46 1.483
537
P MTH007 Methemoglobinemia 46 1.483
538
CNT019 Central Neurocytoma 46 1.483
539
AMN003 Amnestic Disorder 54 1.483
540
THR123 Thrombotic Microangiopathy 40 1.454
541
MYL020 Myelomeningocele 51 1.454
542
P GLC113 Galactosemia I 66 1.454
543
MYL013 Myeloperoxidase Deficiency 44 1.454
544
P PLM034 Pulmonary Emphysema 58 1.454
545
P VNT002 Ventricular Septal Defect 58 1.454
546
CRT013 Carotid Stenosis 51 1.454
547
RBS001 Rabies 58 1.454
548
P SLP005 Sleep Disorder 61 1.454
549
SNL007 Senile Cataract 40 1.454
550
PLM033 Pulmonary Embolism 58 1.454
551
PRL019 Prolidase Deficiency 50 1.450
552
P MYP006 Myopia 56 1.450
553
GNT189 Genetic Prion Disease 20 1.450
554
VSC003 Visceral Leishmaniasis 55 1.446
555
PRG009 Progressive Multifocal Leukoencephalopathy 58 1.446
556
HMZ003 Homozygous Familial Hypercholesterolemia 60 1.431
557
P MYS003 Myasthenia Gravis 68 1.431
558
P DRM053 Dermatitis, Atopic 65 1.431
559
ANG054 Angina Pectoris 66 1.431
560
EPD015 Epidemic Typhus 44 1.431
561
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 1.431
562
CLR109 Colorectal Adenocarcinoma 50 1.431
563
P VSC011 Vasculitis 61 1.431
564
BRN049 Brain Tumor, Childhood 28 1.431
565
MRF001 Marfan Syndrome 76 1.418
566
CLN015 Colon Adenocarcinoma 65 1.418
567
P DYS021 Dysautonomia 38 1.418
568
P ATR011 Atrial Fibrillation 66 1.416
569
P THY032 Thyroiditis 57 1.415
570
MRG013 Mirage Syndrome 44 1.414
571
P MLG074 Malignant Mesenchymoma 40 1.414
572
CNT033 Central Nervous System Cancer 47 1.414
573
SPN041 Spinal Cord Disease 55 1.414
574
P NRV006 Nervous System Cancer 48 1.414
575
MSC157 Muscular Dystrophy, Duchenne Type 79 1.410
576
GRS011 Gerstmann-Straussler Disease 56 1.410
577
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.410
578
P NTR004 Neutropenia 63 1.410
579
LYM017 Lyme Disease 62 1.410
580
AZS001 Azoospermia 45 1.410
581
OVR094 Ovarian Epithelial Cancer 39 1.410
582
P TRN020 Turner Syndrome 67 1.407
583
ANT018 Anthracosis 51 1.381
584
PPL058 Papilloma of Choroid Plexus 55 1.376
585
c DFN116 Deafness, Autosomal Recessive 74 30 1.376
586
FNG017 Fungal Infectious Disease 54 1.376
587
HMN009 Hemangioblastoma 54 1.376
588
PRP030 Purpura 54 1.376
589
BBS001 Babesiosis 49 1.376
590
CRB086 Cerebral Aneurysms 40 1.376
591
c BCT007 Bacterial Meningitis 55 1.363
592
NNS045 Non-Specific Syndromic Intellectual Disability 42 1.363
593
MTH047 Methanol Poisoning 37 1.363
594
CLS049 Classic Phenylketonuria 41 1.363
595
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 1.363
596
HYP017 Hypophosphatemia 49 1.363
597
SCK003 Sickle Cell Anemia 74 1.363
598
CTR172 Citrullinemia, Classic 65 1.363
599
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 52 1.363
600
ACT149 Acetaminophen Metabolism 35 1.363
601
c LRG001 Large Cell Carcinoma 48 1.363
602
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.363
603
P TBR001 Tuberous Sclerosis 69 1.363
604
TYP007 Typhoid Fever 64 1.363
605
MYT011 Myotonia 39 1.363
606
DWR001 Dwarfism 44 1.363
607
AMN007 Aminoacylase 1 Deficiency 33 1.341
608
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.332
609
P PRD006 Prader-Willi Syndrome 61 1.320
610
HRT011 Heart Septal Defect 49 1.318
611
PRS045 Prostatic Hypertrophy 53 1.318
612
PRT038 Protein-Energy Malnutrition 53 1.318
613
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.316
614
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 1.316
615
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.316
616
PLM020 Pleomorphic Xanthoastrocytoma 40 1.316
617
P CWD010 Cowden Syndrome 70 1.316
618
P TRT010 Teratoma 51 1.316
619
P SPN237 Spina Bifida Aperta 19 1.314
620
PRN071 Parenteral Nutrition-Associated Cholestasis 23 1.314
621
P NSP012 Nasopharyngeal Carcinoma 61 1.314
622
P BCK002 Beckwith-Wiedemann Syndrome 62 1.314
623
c BTT014 Beta-Thalassemia 72 1.314
624
KRT019 Keratitis, Hereditary 66 1.314
625
c HNT011 Huntington Disease-Like 3 34 1.314
626
P TTR001 Tetralogy of Fallot 69 1.314
627
c TBR025 Tuberous Sclerosis 1 84 1.314
628
P LKD001 Leukodystrophy 59 1.314
629
PST092 Posttransplant Acute Limbic Encephalitis 28 1.314
630
ANT024 Anthrax Disease 58 1.314
631
LYM027 Lymphopenia 56 1.314
632
TCK001 Tick-Borne Encephalitis 59 1.314
633
P HYP040 Hypospadias 51 1.314
634
INC002 Inclusion Body Myositis 57 1.310
635
ENT004 Enthesopathy 51 1.310
636
c ATM011 Autoimmune Hepatitis 63 1.282
637
P HYD006 Hydrocephalus 61 1.282
638
THY030 Thyroid Gland Disease 50 1.268
639
IRR002 Irritable Bowel Syndrome 65 1.268
640
ENC055 Encephalopathy, Ethylmalonic 51 1.262
641
OTT002 Otitis Media 71 1.262
642
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 1.262
643
P CRP001 Carpal Tunnel Syndrome 66 1.262
644
KPS004 Kaposi Sarcoma 77 1.262
645
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 1.262
646
VRC005 Varicose Veins 60 1.262
647
DGR001 Digeorge Syndrome 62 1.262
648
AVN001 Avian Influenza 61 1.262
649
P LYN001 Lynch Syndrome 76 1.262
650
VGN019 Vaginal Discharge 47 1.262
651
HYP082 Hypopharynx Cancer 47 1.262
652
CHL147 Chlamydia Pneumonia 47 1.262
653
RYS001 Reye Syndrome 49 1.262
654
P CRD119 Cardiac Arrest 67 1.262
655
CRC006 Carcinoid Syndrome 55 1.262
656
ETN001 Eating Disorder 59 1.262
657
c PRS136 Prostate Cancer, Hereditary, 6 33 1.262
658
c PRS130 Prostate Cancer, Hereditary, 8 32 1.262
659
TRN022 Transcobalamin Ii Deficiency 45 1.260
660
NDL024 Nodal Marginal Zone Lymphoma 37 1.252
661
HYP020 Hyperprolactinemia 63 1.252
662
MST020 Mast Cell Activation Syndrome 28 1.252
663
CHG001 Chagas Disease 66 1.246
664
ANT039 Antisynthetase Syndrome 55 1.243
665
P VSC018 Visceral Steatosis 32 1.243
666
P CLS010 Cluster Headache 42 1.229
667
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.229
668
HSH003 Hashimoto Thyroiditis 60 1.213
669
c MLT159 Multiple Endocrine Neoplasia, Type Iib 61 1.209
670
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.209
671
P CHN012 Chondrosarcoma 57 1.209
672
c ACT073 Acute Leukemia 58 1.209
673
PRT036 Peritonitis 65 1.209
674
P DRM010 Dermatomyositis 61 1.209
675
P END044 Endometriosis 62 1.209
676
SPP011 Suppression of Tumorigenicity 12 61 1.207
677
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.207
678
NND010 Nondisjunction 34 1.207
679
SPN221 Spina Bifida Occulta 40 1.207
680
ACT119 Acute Promyelocytic Leukemia 62 1.207
681
c WLM013 Wilms Tumor 1 66 1.207
682
MLD001 Melioidosis 67 1.207
683
LPD007 Lipoadenoma 26 1.207
684
AMB001 Amebiasis 57 1.207
685
CMB007 Combined Immunodeficiency 57 1.207
686
P MMP001 Mumps 57 1.207
687
CNT016 Central Retinal Vein Occlusion 54 1.207
688
P SHR001 Short Bowel Syndrome 53 1.207
689
ENC005 Encephalomalacia 44 1.207
690
CHY002 Chylomicron Retention Disease 64 1.205
691
P ACT010 Acth-Secreting Pituitary Adenoma 61 1.195
692
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.195
693
CNN003 Conn's Syndrome 79 1.195
694
P PLT029 Platelet Groups--Ko System 15 1.181
695
P ART023 Arthropathy 61 1.181
696
P BRB001 Beriberi 44 1.181
697
P PLY014 Polycystic Kidney Disease 69 1.175
698
ITR003 Iatrogenic Creutzfeldt-Jakob Disease 15 1.171
699
P MYL006 Myeloid Leukemia 61 1.171
700
MTH009 Mouth Disease 57 1.171
701
P EYD002 Eye Disease 57 1.171
702
EMB004 Embryonal Carcinoma 56 1.171
703
CND006 Candida Glabrata 30 1.171
704
P SJG008 Sjogren Syndrome 61 1.153
705
AND005 Androgen Insensitivity Syndrome, Mild 21 1.150
706
c MTC063 Mitochondrial Dna Depletion Syndrome 3 51 1.148
707
KSH001 Keshan Disease 34 1.148
708
P FTL001 Fetal Alcohol Syndrome 55 1.148
709
P CRB048 Cerebral Cavernous Malformations 63 1.148
710
c PRG020 Paragangliomas 3 39 1.148
711
c MCR312 Microphthalmia, Syndromic 10 40 1.148
712
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 1.148
713
PRM329 Premature Aging 36 1.148
714
CTN007 Cutaneous Leishmaniasis 62 1.148
715
PLM014 Pleomorphic Adenoma 51 1.148
716
CRB001 Cerebral Lymphoma 36 1.148
717
DFF036 Differentiated Thyroid Carcinoma 51 1.148
718
GST040 Gastric Adenocarcinoma 67 1.148
719
OLF005 Olfactory Neuroblastoma 46 1.148
720
MRS001 Marasmus 42 1.148
721
LWC001 Low Compliance Bladder 45 1.148
722
P INT143 Interstitial Cystitis 60 1.148
723
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.148
724
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 48 1.148
725
P BRN022 Bronchiectasis 60 1.148
727
CVR010 Cavernous Malformation 30 1.148
728
SPR166 Sporadic Fatal Insomnia 14 1.131
729
P EXN002 Exanthem 58 1.131
730
YLL002 Yellow Fever 61 1.131
731
P OPT006 Optic Nerve Disease 58 1.131
732
c SRC023 Sarcoidosis 2 44 1.105
733
PLS009 Plasma Cell Neoplasm 64 1.105
734
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.105
735
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.100
736
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 46 1.100
737
GLY010 Glycine Encephalopathy 57 1.100
738
P FML068 Familial Hypocalciuric Hypercalcemia 55 1.100
739
ADG002 Audiogenic Seizures 25 1.100
740
WLD005 Wild Type Attr Amyloidosis 29 1.100
741
SLC006 Silicosis 56 1.100
742
CHN004 Chondroblastoma 41 1.100
743
PLZ002 Pelizaeus-Merzbacher-Like Disease 37 1.100
744
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.090
745
P RTT002 Rett Syndrome 79 1.090
746
PRS129 Prostatic Hyperplasia, Benign 49 1.090
747
HLC007 Helicobacter Pylori Infection 67 1.090
748
NPH009 Nephrolithiasis 54 1.090
749
PRS021 Prostatic Adenoma 43 1.090
750
c ALP101 Alpha-Thalassemia 62 1.083
751
FML037 Female Breast Cancer 51 1.083
752
BRR014 Barrett Esophagus 66 1.083
753
SXL003 Sexual Disorder 49 1.083
754
ANT009 Antithrombin Iii Deficiency 59 1.083
755
P TRT019 Torticollis 47 1.083
756
c PNC106 Pancreatic Agenesis 1 51 1.083
757
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.083
758
RTC009 Reticulum Cell Sarcoma 44 1.083
759
P ANG001 Angelman Syndrome 65 1.083
760
STS002 Situs Inversus 45 1.083
761
OVR059 Ovary Adenocarcinoma 49 1.083
762
P CHR071 Charcot-Marie-Tooth Disease 64 1.083
763
PLC002 Plica Syndrome 35 1.083
764
DYS015 Dysentery 50 1.083
765
PYR004 Pyuria 36 1.083
766
TTH006 Tooth Disease 51 1.083
767
SYN007 Synovitis 55 1.083
768
PNC034 Pancreas Disease 50 1.083
769
MTH081 Mthfr Gene Variant 10 1.083
770
ARG007 Argininemia 58 1.064
771
c MST023 Mesothelioma, Malignant 56 1.063
772
RTN017 Retinal Detachment 60 1.047
773
VLV047 Volvulus of Midgut 52 1.047
774
c LKM063 Leukemia, Chronic Myeloid 71 1.047
775
P PLY041 Polymyositis 59 1.047
776
P NPH012 Nephrotic Syndrome 60 1.047
777
INT066 Interstitial Lung Disease 60 1.047
778
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 1.039
779
MTH040 Methylmalonyl-Coa Epimerase Deficiency 26 1.039
780
INT002 Intermittent Claudication 61 1.017
781
P ESP024 Esophagitis 60 1.017
782
PNM013 Pneumococcal Meningitis 43 1.012
783
CYN003 Cyanide Poisoning 22 1.012
784
DRV001 Dravet Syndrome 69 1.012
785
c ANM038 Anemia, Autoimmune Hemolytic 64 1.012
786
c OPT053 Optic Atrophy 1 62 1.012
788
MYL009 Myelodysplastic Syndrome 67 1.012
789
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 37 1.012
790
P CNG436 Congenital Disorder of Deglycosylation 51 1.012
791
c ERY064 Erythrocytosis, Familial, 6 30 1.012
792
RNL077 Renal Fibrosis 46 1.012
793
CWP001 Cowpox 45 1.012
794
MNG007 Manganese Poisoning 28 1.012
795
CLL003 Cellulitis 53 1.012
796
P RST002 Restrictive Cardiomyopathy 54 1.012
797
P ACN011 Acne 57 1.012
798
HYP005 Hypokalemia 55 1.012
799
P INT070 Intestinal Obstruction 57 1.012
800
PLR008 Pleurisy 50 1.012
801
P MGR001 Migraine Without Aura 49 1.012
802
LYD001 Leydig Cell Tumor 45 1.012
803
TRC008 Trachoma 53 1.012
804
ART004 Aortic Atherosclerosis 47 1.012
805
P LRY044 Larynx Cancer 54 1.012
806
P MNN013 Meningitis 65 1.012
807
GMS001 Gemistocytic Astrocytoma 32 1.012
808
LTH004 Lathyrism 15 1.012
809
CRY036 Cryptogenic Cirrhosis 36 1.012
810
P FML187 Familial Hypertension 34 1.012
811
ACT228 Acute Radiation Syndrome 30 1.003
812
P PRP003 Porphyria Cutanea Tarda 66 1.003
813
c BPL002 Bipolar I Disorder 47 1.003
814
BCT004 Bacteriuria 47 1.003
815
ANT019 Anterograde Amnesia 38 1.003
816
PST028 Post-Traumatic Stress Disorder 59 1.003
817
FRN006 Frontotemporal Dementia 68 1.002
818
c MCL062 Mucolipidosis Ii Alpha/beta 68 1.002
819
c THR082 Thrombophilia Due to Activated Protein C Resistance 59 1.002
820
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.002
821
GST050 Gastrointestinal System Disease 55 1.002
822
P HRD217 Hereditary Optic Neuropathy 36 0.956
823
AND002 Androgen Insensitivity Syndrome 63 0.956
824
PRP080 Peripheral Artery Disease 54 0.956
825
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.956
826
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.956
827
ALP103 Alpha-1-Antitrypsin Deficiency 68 0.956
828
P ASP006 Aspergillosis 72 0.956
829
EXT007 Extracutaneous Mastocytoma 38 0.956
830
MST004 Mast Cell Neoplasm 42 0.956
831
TRT001 Teratocarcinoma 42 0.956
832
INT271 Interstitial Lung and Liver Disease 40 0.956
833
TLN003 Telangiectasis 51 0.956
834
BLR001 Biliary Atresia 55 0.956
835
BRC012 Brucellosis 66 0.956
836
P RHN004 Rhinitis 57 0.956
837
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.956
838
P EPD016 Epidermolysis Bullosa 53 0.956
839
LYS002 Lysosomal Storage Disease 51 0.956
840
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.956
841
MTC005 Mitochondrial Metabolism Disease 45 0.936
842
c PNC108 Pancreatitis, Hereditary 69 0.936
843
GLS018 Glass Syndrome 61 0.934
844
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.934
845
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 41 0.931
846
SDD008 Sudden Sensorineural Hearing Loss 41 0.931
847
CRB151 Cerebral Creatine Deficiency Syndrome 1 50 0.931
848
LSC001 Lesch-Nyhan Syndrome 62 0.931
849
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 64 0.931
850
AND020 Androgen Insensitivity, Partial 55 0.931
851
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 0.931
852
PLS025 Plasmablastic Lymphoma 56 0.931
853
c ATS006 Autosomal Recessive Nonsyndromic Deafness 27 0.931
854
c 2HY001 2-Hydroxyglutaric Aciduria 38 0.931
855
DBT090 Diabetes and Deafness, Maternally Inherited 45 0.931
856
TRD006 Tardive Dyskinesia 53 0.931
857
c CHL119 Cholangitis, Primary Sclerosing 58 0.931
858
CHR072 Chordoma 57 0.931
859
GLB001 Gilbert Syndrome 53 0.931
860
HNZ004 Heinz Body Anemias 40 0.931
861
ADN011 Adenoid Cystic Carcinoma 68 0.931
862
P HYP077 Hypertrichosis 46 0.931
863
URT010 Ureteral Obstruction 45 0.931
864
PDT001 Pediatric Lymphoma 27 0.931
865
P RNV001 Renovascular Hypertension 49 0.931
866
P PLY018 Polycythemia 56 0.931
867
P PLL002 Pellagra 46 0.931
868
THY006 Thymus Lymphoma 27 0.931
869
P SCL009 Sclerosing Cholangitis 48 0.931
870
P DDN001 Duodenal Ulcer 53 0.931
871
GLS001 Gliosarcoma 64 0.931
872
P CNG003 Congenital Dyserythropoietic Anemia 48 0.931
873
SPT005 Spotted Fever 49 0.931
874
HYP043 Hyperandrogenism 48 0.931
875
GST029 Gastric Cardia Adenocarcinoma 29 0.931
876
P INT068 Intestinal Disease 53 0.931
877
TLR001 Tularemia 56 0.931
878
c NNS007 Nonsyndromic Deafness 33 0.931
879
AML004 Ameloblastic Carcinoma 39 0.931
880
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 0.931
881
TTT001 Tatton-Brown-Rahman Syndrome 46 0.908
882
CLF004 Cleft Lip/palate 57 0.907
883
P AST005 Asthma 76 0.907
884
P LKM071 Leukemia, Chronic Lymphocytic 75 0.907
885
BTN004 Biotin Deficiency 45 0.907
886
WST001 West Syndrome 59 0.907
887
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.907
888
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.907
889
P RBL001 Rubella 58 0.907
890
P THR014 Thrombocytopenia 66 0.907
891
P GRF003 Graft-Versus-Host Disease 71 0.907
892
PNC001 Pancytopenia 53 0.907
893
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.907
894
P NRV007 Nervous System Disease 67 0.907
895
CHR682 Chronic Bilirubin Encephalopathy 37 0.892
896
c FML001 Familial Atrial Fibrillation 65 0.892
897
PTT057 Pituitary Adenoma 4, Acth-Secreting 48 0.892
898
c MJR006 Major Affective Disorder 5 32 0.892
899
c MJR023 Major Affective Disorder 7 33 0.892
900
c MJR004 Major Affective Disorder 4 28 0.892
901
c MJR003 Major Affective Disorder 6 32 0.892
902
c MJR008 Major Affective Disorder 2 34 0.892
903
FNC007 Functioning Pituitary Adenoma 42 0.892
904
AMN002 Amino Acid Metabolic Disorder 39 0.892
905
PTT003 Pituitary-Dependent Cushing's Disease 39 0.892
906
MYF002 Myofascial Pain Syndrome 46 0.892
907
PPL001 Papillary Adenoma 44 0.892
908
P INB001 Inborn Amino Acid Metabolism Disorder 11 0.892
909
HLT002 Halothane Hepatitis 31 0.878
910
FCS002 Fucosidosis 62 0.855
911
P ATX030 Ataxia-Telangiectasia 80 0.855
912
P CLC063 Celiac Disease 1 66 0.855
913
P HYP111 Hyperprolinemia 45 0.855
914
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.855
915
CMP034 Complete Androgen Insensitivity Syndrome 55 0.855
916
SCH038 Schopf-Schulz-Passarge Syndrome 51 0.855
917
GYR004 Gyrate Atrophy of Choroid and Retina 58 0.855
918
MYT030 Myotonia, Potassium-Aggravated 46 0.855
919
LRN003 Learning Disability 49 0.855
920
P PRD021 Periodic Paralysis 41 0.855
921
TRC003 Trichomoniasis 53 0.855
922
P HYP061 Hypertrophic Cardiomyopathy 69 0.855
923
ALC009 Alcoholic Liver Cirrhosis 54 0.855
924
ATN004 Autonomic Neuropathy 42 0.855
925
P BND020 Bone Disease 59 0.855
926
P SBS003 Substance Abuse 54 0.855
927
LNS001 Lens Subluxation 39 0.855
928
P OST001 Osteopetrosis 71 0.855
929
P HRD011 Hereditary Spherocytosis 64 0.855
930
HYP014 Hyperuricemia 51 0.855
931
P TXP001 Toxoplasmosis 60 0.855
932
PLY100 Polyploidy 36 0.835
933
P ALB003 Albinism-Deafness Syndrome 34 0.835
934
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.835
935
c ATR062 Atrial Septal Defect 1 39 0.835
936
c L2H001 L-2-Hydroxyglutaric Aciduria 49 0.835
937
P FML011 Familial Adenomatous Polyposis 71 0.835
938
c VNW010 Von Willebrand Disease, Type 2 48 0.835
939
c RTN066 Retinitis Pigmentosa 4 42 0.835
940
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 0.835
941
c ATM045 Autoimmune Glomerulonephritis 35 0.835
942
BTT017 Beta-Thalassemia Major 51 0.835
943
LPT014 Leptin Deficiency or Dysfunction 78 0.835
944
ARM004 Aromatase Excess Syndrome 51 0.835
945
HND015 Hand Skill, Relative 30 0.835
946
P FBR003 Fibrous Histiocytoma 43 0.835
947
BRN018 Borna Disease 36 0.835
948
CMP010 Complex Regional Pain Syndrome 60 0.835
949
MLT006 Multidrug-Resistant Tuberculosis 47 0.835
950
HRT012 Heart Valve Disease 53 0.835
9