Search results for Manganese

1401 hits were found for Manganese

# Family MCID Name MIFTS Score
1
MNG007 Manganese Poisoning 28 40.461
2
DSR032 Disorder of Manganese Transport 7 20.074
3
P HYP821 Hypermanganesemia with Dystonia 26 12.489
4
P PRK039 Parkinsonism 55 9.731
5
IRN002 Iron Metabolism Disease 56 6.507
6
HPT019 Hepatic Encephalopathy 59 5.877
7
P TRM003 Tremor 50 5.617
8
P ENC018 Encephalopathy 62 5.601
9
P PRK057 Parkinson Disease, Late-Onset 79 5.457
10
CHL068 Cholestasis 61 5.173
11
HPT004 Hepatic Coma 43 4.994
12
RPD005 Rapidly Involuting Congenital Hemangioma 48 4.985
13
P DYS154 Dystonia 64 4.834
14
P NRB001 Neuroblastoma 66 4.352
15
P LTR001 Lateral Sclerosis 57 4.126
16
c AMY091 Amyotrophic Lateral Sclerosis 1 87 4.081
17
P LVR013 Liver Disease 68 3.941
18
c ATR087 Atrial Standstill 1 74 3.875
19
P HNT016 Huntington Disease 73 3.657
20
48X005 48,xyyy 39 3.596
21
P MVM001 Movement Disease 61 3.539
22
c HYP716 Hypermanganesemia with Dystonia 1 34 3.536
23
AGN016 Aging 53 3.314
24
ISC004 Ischemia 61 3.198
25
NTR005 Nutritional Deficiency Disease 60 3.146
26
LVR012 Liver Cirrhosis 62 3.080
27
HYP266 Hypoxia 56 3.058
28
P SZR006 Seizure Disorder 69 3.032
29
c CNG498 Congenital Disorder of Glycosylation, Type Iin 41 2.994
30
P PRN023 Prion Disease 60 2.986
31
HMS001 Hemosiderosis 48 2.974
32
P RRH023 Rare Hereditary Hemochromatosis 52 2.974
33
c DLT002 Dilated Cardiomyopathy 79 2.933
34
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.932
35
P ATT013 Attention Deficit-Hyperactivity Disorder 65 2.919
36
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 2.903
37
P GLM040 Glioma Susceptibility 1 70 2.890
38
c HYP713 Hypermanganesemia with Dystonia 2 35 2.889
39
P PNC035 Pancreatic Cancer 87 2.833
40
GLL048 Glial Tumor 51 2.766
41
GLM045 Glioma 62 2.742
42
P PHC003 Pheochromocytoma 70 2.728
43
ADR040 Adrenal Gland Pheochromocytoma 45 2.728
44
MLG169 Malignant Astrocytoma 57 2.723
45
P ESP024 Esophagitis 60 2.691
46
P OVR042 Ovarian Cancer 88 2.582
47
DRM006 Dermatitis 61 2.574
48
P PLY018 Polycythemia 56 2.546
49
GLB002 Glioblastoma 67 2.524
50
P EPL164 Epilepsy 70 2.490
51
P PNC044 Pancreatitis 61 2.457
52
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 2.452
53
c HMC039 Hemochromatosis, Type 1 73 2.403
54
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.386
55
HRW001 Hair Whorl 35 2.374
56
P HPT021 Hepatitis 68 2.360
57
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.359
58
CHL123 Chlamydia 58 2.272
59
HLX001 Helix Syndrome 47 2.224
60
SQM006 Squamous Cell Carcinoma 59 2.219
61
ANT018 Anthracosis 50 2.214
62
P PNM006 Pneumoconiosis 55 2.214
63
DYS031 Dystonia/parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease 14 2.208
64
P ALZ034 Alzheimer Disease 87 2.180
65
CNT047 Contact Dermatitis 56 2.177
66
c TYP008 Type 1 Diabetes Mellitus 77 2.154
67
P DRM053 Dermatitis, Atopic 65 2.118
68
SCR011 Scrapie 39 2.106
69
PPL052 Papillomatosis, Confluent and Reticulated 34 2.094
70
DFC004 Deficiency Anemia 74 2.093
71
P HYP086 Hypothyroidism 68 2.071
72
CRB004 Cerebral Artery Occlusion 45 2.038
73
MCS002 Mucositis 55 2.014
74
P BNG032 Benign Mesothelioma 53 2.007
75
SVR001 Severe Acute Respiratory Syndrome 68 1.983
76
SLC035 Slc39a14 Deficiency 8 1.948
77
ESP021 Esophageal Cancer 84 1.929
78
P FBR017 Fibrosarcoma 55 1.929
79
STM007 Stomatitis 52 1.913
80
ENT011 Enterocolitis 55 1.897
81
KFR001 Kufor-Rakeb Syndrome 59 1.884
82
c TYP009 Type 2 Diabetes Mellitus 91 1.869
83
P MLT020 Multiple Sclerosis 79 1.865
84
GTR002 Goiter 52 1.858
85
P BRS047 Breast Cancer 97 1.845
86
TLN003 Telangiectasis 51 1.843
87
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.836
88
c ACT027 Acute Pancreatitis 60 1.810
89
HYP066 Hyperglycemia 60 1.809
90
P FNG006 Feingold Syndrome 1 61 1.804
91
BRN024 Bronchitis 67 1.801
92
DPH001 Diphtheria 59 1.799
93
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.795
94
CHR073 Choreatic Disease 53 1.795
95
FTT001 Fatty Liver Disease 61 1.789
96
HGH043 High Grade Glioma 46 1.788
97
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.786
98
c HPT003 Hepatitis a 63 1.785
99
P MYC007 Myocardial Infarction 69 1.778
100
c CNT035 Central Nervous System Disease 53 1.775
101
c ATS007 Autism Spectrum Disorder 71 1.760
102
P ATS364 Autism 72 1.760
103
47X002 47,xyy 47 1.756
104
P HPT023 Hepatocellular Carcinoma 95 1.755
105
TRD006 Tardive Dyskinesia 53 1.734
106
BRN071 Brain Injury 50 1.733
107
P BCL017 B-Cell Lymphoma 57 1.728
108
P HYP061 Hypertrophic Cardiomyopathy 68 1.721
109
HYP005 Hypokalemia 55 1.715
110
RCK004 Rickets 64 1.703
111
LYM019 Lymphosarcoma 46 1.699
112
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.686
113
CRH001 Crohn's Disease 80 1.684
114
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.677
115
BNR002 Bone Resorption Disease 47 1.668
116
SVR004 Severe Combined Immunodeficiency 70 1.666
117
P ADN016 Adenocarcinoma 63 1.651
118
P END033 Endocarditis 58 1.641
119
PSD088 Pseudobulbar Affect 33 1.638
120
MNN028 Mononeuropathy of the Median Nerve, Mild 47 1.633
121
SPN186 Spinal Cord Injury 60 1.633
122
P ATX030 Ataxia-Telangiectasia 80 1.633
123
ANX010 Anxiety 70 1.617
124
P NRN021 Neuronal Ceroid Lipofuscinosis 64 1.612
125
CLT003 Colitis 63 1.603
126
HVY002 Heavy Metal Poisoning 22 1.602
127
c CNG411 Congenital Disorder of Glycosylation, Type in 66 1.580
128
P CRD246 Cardiovascular System Disease 55 1.572
129
NNL006 Non-Alcoholic Steatohepatitis 54 1.565
130
c MST023 Mesothelioma, Malignant 56 1.560
131
OCL069 Ocular Motor Apraxia 57 1.557
132
DNT012 Dental Caries 53 1.549
133
TXC002 Toxic Encephalopathy 51 1.542
134
c MCR130 Microvascular Complications of Diabetes 6 41 1.533
135
PRT037 Pertussis 49 1.533
136
CYT002 Cytokine Deficiency 43 1.526
137
c MCR115 Microvascular Complications of Diabetes 5 65 1.519
138
ANX004 Anoxia 40 1.519
139
P LNG064 Lung Cancer Susceptibility 3 69 1.516
140
c MCR133 Microvascular Complications of Diabetes 4 41 1.508
141
c MCR113 Microvascular Complications of Diabetes 3 52 1.508
142
c MCR120 Microvascular Complications of Diabetes 7 47 1.508
143
CVD001 Covid-19 59 1.504
144
P MJR001 Major Depressive Disorder 68 1.495
145
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.483
146
LYM017 Lyme Disease 63 1.481
147
P THY032 Thyroiditis 56 1.474
148
HMN044 Human Immunodeficiency Virus Type 1 76 1.472
149
STT001 Status Epilepticus 58 1.462
150
NPH018 Nephrogenic Systemic Fibrosis 48 1.462
151
P LNG032 Lung Cancer 98 1.462
152
P SCH015 Schizophrenia 74 1.443
153
PST011 Pustulosis of Palm and Sole 52 1.435
154
P PSR002 Psoriasis 63 1.435
156
DWN001 Down Syndrome 70 1.430
157
RHB024 Rhabdomyosarcoma 2 65 1.429
158
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.418
159
INF034 Infective Endocarditis 53 1.417
160
HDN002 Head Injury 44 1.417
161
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 1.412
162
LPD008 Lipid Metabolism Disorder 61 1.409
163
c ACT134 Acute Liver Failure 57 1.409
164
P LYM118 Lymphoma 66 1.403
165
c PCH010 Pachyonychia Congenita 3 43 1.400
166
BLR001 Biliary Atresia 55 1.400
167
OST012 Osteoarthritis 77 1.394
168
ALC007 Alcohol Dependence 65 1.388
169
P GST053 Gastric Cancer 82 1.364
170
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.362
171
EXT034 Extrinsic Allergic Alveolitis 56 1.361
172
P MRC003 Mercury Poisoning 48 1.354
173
P MLN008 Melanoma 75 1.352
174
PRM236 Primary Biliary Cholangitis 62 1.351
175
TRM010 Traumatic Brain Injury 50 1.351
176
THY030 Thyroid Gland Disease 50 1.339
177
LNG099 Lung Disease 62 1.334
178
URM002 Uremia 47 1.326
179
OST159 Osteogenic Sarcoma 66 1.320
180
P SKN015 Skin Carcinoma 71 1.320
181
c BRN108 Branchiootic Syndrome 1 63 1.319
182
P PNM007 Pneumonia 64 1.302
183
BRN004 Brain Edema 54 1.298
184
c HYP836 Hypercholesterolemia, Familial, 1 73 1.298
185
DWR001 Dwarfism 44 1.298
186
P MYC008 Myocarditis 59 1.297
187
P PRC019 Precocious Puberty 48 1.294
188
P CHR345 Chronic Pain 50 1.294
189
P EYD002 Eye Disease 57 1.290
190
INS001 Insulinoma 59 1.286
191
P PRS038 Personality Disorder 65 1.282
192
P TMP001 Temporal Lobe Epilepsy 49 1.281
193
ADN018 Adenoma 58 1.276
194
c PRC016 Pre-Eclampsia 64 1.276
195
P FRD001 Friedreich Ataxia 62 1.272
196
P MTR014 Motor Neuron Disease 65 1.272
197
P PLY011 Polycystic Ovary Syndrome 57 1.265
198
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 1.261
199
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.252
200
P NRV007 Nervous System Disease 65 1.252
201
PRN019 Perinatal Necrotizing Enterocolitis 60 1.239
202
CRT072 Creutzfeldt-Jakob Disease 67 1.237
203
IRN001 Iron Deficiency Anemia 58 1.231
204
P MYC084 Mycobacterium Tuberculosis 1 68 1.220
205
BRR014 Barrett Esophagus 66 1.220
206
P PLY019 Polyneuropathy 52 1.220
207
c SML038 Small Cell Cancer of the Lung 68 1.215
208
WLS001 Wilson Disease 70 1.212
209
P SHR001 Short Bowel Syndrome 53 1.212
210
MRV001 Morvan's Fibrillary Chorea 11 1.208
211
LRN003 Learning Disability 49 1.204
212
MLG079 Malignant Pleural Mesothelioma 42 1.204
213
MNT002 Mental Depression 56 1.198
214
MLD018 Mild Cognitive Impairment 48 1.186
215
IMM167 Immune Deficiency Disease 76 1.186
216
P ANR048 Aniridia 1 66 1.186
217
PRM013 Premature Menopause 57 1.186
218
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.177
219
P ASP006 Aspergillosis 71 1.177
220
PRL019 Prolidase Deficiency 50 1.174
221
P ALC033 Alcohol Use Disorder 67 1.174
222
DMP001 Dumping Syndrome 43 1.167
223
P PRD008 Periodontitis 63 1.167
224
P PRP019 Peripheral Nervous System Disease 57 1.158
225
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.150
226
c PRM196 Premature Ovarian Failure 1 58 1.148
227
LNG031 Lung Benign Neoplasm 51 1.148
228
c OVR114 Ovarian Cancer 1 60 1.148
229
BLR013 Biliary Tract Cancer 43 1.148
230
P PRS040 Prostate Cancer 95 1.147
231
c PLM121 Pulmonary Hypertension, Primary, 4 28 1.147
232
PSY004 Psychotic Disorder 66 1.147
233
c ACT075 Acute Myocardial Infarction 55 1.147
234
P PLM036 Pulmonary Fibrosis 65 1.138
235
BNG091 Benign Chronic Pemphigus 56 1.134
236
ATH013 Atherosclerosis Susceptibility 63 1.128
237
P SLP005 Sleep Disorder 61 1.128
238
P MSC005 Muscular Dystrophy 66 1.128
239
P SPP010 Suppressor of Tumorigenicity 3 50 1.119
240
SKN016 Skin Disease 63 1.119
241
P DBT009 Diabetes Mellitus 67 1.107
242
DPR016 Depression 64 1.107
243
P SPR120 Supranuclear Palsy, Progressive, 1 68 1.096
244
MST005 Mastitis 52 1.096
245
PST092 Posttransplant Acute Limbic Encephalitis 29 1.096
246
CNG034 Congestive Heart Failure 69 1.074
247
FBR047 Fibromyalgia 57 1.074
248
BRN028 Brain Cancer 73 1.074
249
MSC157 Muscular Dystrophy, Duchenne Type 78 1.060
250
P SBS003 Substance Abuse 54 1.060
251
P ENC004 Encephalitis 61 1.060
252
P TRC086 Trichohepatoenteric Syndrome 1 59 1.058
253
CRR017 Curry-Jones Syndrome 36 1.058
254
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.058
255
CMR002 Coumarin Resistance 59 1.058
256
ATN011 Autoinflammation with Infantile Enterocolitis 46 1.058
257
BRK012 Broken Heart Syndrome 42 1.058
258
P NRP001 Neuropathy 59 1.051
259
P NSP012 Nasopharyngeal Carcinoma 60 1.050
260
SPC005 Speech Disorder 46 1.050
261
P HRT032 Heart Disease 84 1.049
262
KRT002 Keratomalacia 54 1.049
263
TRN015 Transient Cerebral Ischemia 62 1.047
264
P OPT006 Optic Nerve Disease 57 1.047
265
OCC016 Occupational Asthma 33 1.047
266
PLG002 Plague 58 1.047
267
P CLR023 Colorectal Cancer 100 1.042
268
ORL015 Oral Squamous Cell Carcinoma 43 1.034
269
P RSP003 Respiratory Failure 73 1.034
270
P ART021 Arteriosclerosis 53 1.034
271
BLR008 Bilirubin Metabolic Disorder 57 1.034
272
P HYP076 Hyperthyroidism 53 1.034
273
c HPT073 Hepatitis C Virus 70 1.020
274
PRT013 Portal Hypertension 59 1.013
275
PLY150 Polykaryocytosis Inducer 29 1.005
276
CHR100 Chronic Ulcer of Skin 57 1.005
277
P PLM037 Pulmonary Hypertension 69 1.005
278
BRN056 Bronchopulmonary Dysplasia 57 1.005
279
P HRP006 Herpes Simplex 65 1.005
280
P OVR082 Overgrowth Syndrome 41 1.005
281
P INF032 Infertility 60 1.003
282
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.993
283
MYL069 Myeloma, Multiple 76 0.990
284
HRN029 Hearing Loss, Noise-Induced 37 0.973
285
CRV035 Cervical Cancer 72 0.973
286
PPL022 Papilloma 53 0.973
287
SQM002 Squamous Cell Papilloma 45 0.973
288
c CHR684 Chronic Kidney Disease 73 0.972
289
c CNG383 Congenital Disorder of Glycosylation, Type Iik 43 0.961
290
P MLN007 Male Infertility 56 0.961
291
END086 End Stage Renal Disease 54 0.961
292
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.938
293
P MYP004 Myopathy 67 0.937
294
P MTC069 Mitochondrial Disorders 57 0.937
295
BRN032 Brain Glioma 45 0.936
296
TNG009 Tongue Squamous Cell Carcinoma 43 0.936
297
PHR003 Pharyngitis 57 0.936
298
KWS001 Kwashiorkor 44 0.936
299
SPN035 Spindle Cell Sarcoma 51 0.936
300
MDD011 Mood Disorder 61 0.936
301
PPT001 Peptic Esophagitis 51 0.936
302
SRC014 Sarcoma 64 0.936
303
P HYP069 Hyperparathyroidism 62 0.935
304
c SCN007 Secondary Hyperparathyroidism 50 0.927
305
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.925
306
MLT157 Multiple System Atrophy 1 69 0.925
307
IMP005 Impotence 52 0.925
308
P GST044 Gastritis 55 0.925
309
ULC004 Ulcerative Colitis 74 0.925
310
P RTN016 Retinal Degeneration 52 0.925
311
KRT009 Keratosis 52 0.919
312
TTN003 Tetanus 64 0.912
313
ATS010 Autosomal Recessive Disease 42 0.899
314
HLC007 Helicobacter Pylori Infection 67 0.899
315
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.899
316
P SYS005 Systemic Scleroderma 73 0.899
317
AMN003 Amnestic Disorder 53 0.899
318
PCD001 Pica Disease 38 0.899
319
TXC005 Toxic Shock Syndrome 61 0.899
320
CHL014 Cholera 62 0.893
321
PFF001 Pfeiffer Syndrome 77 0.891
322
THY006 Thymus Lymphoma 27 0.891
323
OCL006 Ocular Hypertension 53 0.891
324
PRR015 Preauricular Fistulae, Congenital 20 0.885
325
NRT004 Neuritis 53 0.885
326
P KDN018 Kidney Disease 71 0.885
327
PLM010 Pulmonary Edema 54 0.885
328
P UVT001 Uveitis 57 0.885
329
URL001 Urolithiasis 45 0.885
330
P HYP265 Hypotonia 42 0.885
331
P VSC007 Vascular Disease 62 0.871
332
P RHN004 Rhinitis 56 0.871
333
c ESS001 Essential Tremor 56 0.871
334
P CHL066 Cholangitis 51 0.871
335
P AMY004 Amyloidosis 69 0.871
336
CHP002 Chops Syndrome 47 0.862
337
CCC002 Coccidiosis 50 0.862
338
ALL010 Allergic Contact Dermatitis 55 0.862
339
BBN001 Bubonic Plague 40 0.862
340
P DMN002 Dementia 65 0.858
341
c HNT004 Huntington Disease-Like 2 51 0.855
342
GST092 Gastroesophageal Reflux 59 0.855
343
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.855
344
P ART022 Arthritis 70 0.855
345
HYP056 Hypoglycemia 65 0.848
346
c DWL002 Dowling-Degos Disease 1 58 0.839
347
ASB001 Asbestosis 47 0.839
348
CHL067 Cholecystitis 59 0.839
349
GST045 Gastroenteritis 58 0.839
350
c HPT001 Hepatitis C 61 0.839
351
c VRL010 Viral Hepatitis 52 0.839
352
END028 Endemic Goiter 36 0.839
353
P MNN013 Meningitis 65 0.839
354
ASB003 Asbestos Intoxication 32 0.839
355
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.838
356
MTH071 Methane Production 24 0.828
357
BRN002 Bronchiolitis 57 0.828
358
P CRN300 Coronary Heart Disease 1 73 0.821
359
STR067 Stroke, Ischemic 79 0.821
360
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.821
361
P NPH012 Nephrotic Syndrome 61 0.821
362
CLR109 Colorectal Adenocarcinoma 50 0.821
363
CNN005 Connective Tissue Disease 66 0.821
364
P LPS004 Lupus Erythematosus 61 0.821
367
GNT167 Genetic Obesity 33 0.821
368
RNL077 Renal Fibrosis 46 0.807
369
ATM095 Autoimmune Disease 61 0.807
370
RHM034 Rahman Syndrome 37 0.802
371
CRD132 Cardiac Conduction Defect 59 0.802
372
CMB007 Combined Immunodeficiency 56 0.802
373
P FLL037 Follicular Lymphoma 66 0.802
374
P DRR001 Diarrhea 55 0.802
375
P MYP006 Myopia 55 0.802
376
ALC006 Alcoholic Hepatitis 61 0.802
377
P MYL006 Myeloid Leukemia 60 0.802
378
ALL014 Allergic Encephalomyelitis 34 0.802
379
P PRP029 Porphyria 60 0.785
380
ALL029 Allergic Disease 61 0.785
381
CNG491 Congenital Portosystemic Shunt 17 0.785
382
DSS008 Disease of Mental Health 74 0.784
383
ACT119 Acute Promyelocytic Leukemia 62 0.780
384
c SYS001 Systemic Lupus Erythematosus 85 0.780
385
SPP011 Suppression of Tumorigenicity 12 61 0.780
386
c LKM061 Leukemia, Acute Myeloid 83 0.780
387
c CHL119 Cholangitis, Primary Sclerosing 57 0.780
388
PNM005 Pneumonic Plague 46 0.780
389
ACR007 Acromegaly 70 0.780
390
P SCL009 Sclerosing Cholangitis 46 0.780
391
ACT003 Acute Kidney Tubular Necrosis 46 0.780
392
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.780
393
MTC005 Mitochondrial Metabolism Disease 44 0.780
394
NRL016 Neural Tube Defects 80 0.774
395
CHR028 Chronic Wasting Disease 33 0.774
396
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.762
397
P OST002 Osteoporosis 76 0.762
398
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.762
399
ACT078 Acute Porphyria 50 0.762
400
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.756
401
P SRC025 Sarcoidosis 1 70 0.756
402
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.756
403
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.756
404
LGG001 Legg-Calve-Perthes Disease 59 0.756
405
P PLY041 Polymyositis 58 0.756
406
PLM012 Pulmonary Sarcoidosis 52 0.756
407
BRC012 Brucellosis 66 0.756
408
P LRY019 Laryngitis 53 0.756
409
P GRV001 Graves' Disease 54 0.756
410
MCR018 Microcytic Anemia 46 0.756
411
P URT039 Urticaria 57 0.756
412
MNN043 Meningioma, Familial 79 0.750
413
BCT022 Bacterial Infectious Disease 55 0.750
414
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.750
415
SCR001 Secretory Meningioma 40 0.750
416
INT395 Intracranial Meningioma 47 0.750
417
P MCR129 Microvascular Complications of Diabetes 1 67 0.747
418
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.747
419
CRV043 Cervical Dystonia 46 0.737
420
P BLD134 Bladder Cancer 79 0.737
421
NPH009 Nephrolithiasis 54 0.737
422
P BRS044 Breast Adenocarcinoma 58 0.737
423
c HNT010 Huntington Disease-Like 1 54 0.727
424
HYP017 Hypophosphatemia 49 0.727
425
MYM001 Myoma 54 0.727
426
ALC005 Alcoholic Pancreatitis 38 0.727
427
PRN009 Paranoid Schizophrenia 49 0.727
428
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 0.727
429
OTT002 Otitis Media 70 0.723
430
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.723
431
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.723
432
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.723
433
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.723
434
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.723
435
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.723
436
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.723
437
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.723
438
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.723
439
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.723
440
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.723
441
ATN005 Autonomic Dysfunction 45 0.723
442
HYP264 Hypertonia 35 0.723
443
c HNT011 Huntington Disease-Like 3 33 0.710
444
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.710
445
c ACT071 Acute Kidney Failure 60 0.710
446
PRT058 Pure Autonomic Failure 58 0.710
447
ART140 Arteries, Anomalies of 52 0.695
448
c EXD008 Exudative Vitreoretinopathy 1 71 0.695
449
LPP008 Lipoprotein Quantitative Trait Locus 65 0.695
450
P KDN017 Kidney Cancer 60 0.695
451
GLC003 Glucose Intolerance 53 0.695
452
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.695
453
P INF038 Influenza 68 0.695
454
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.690
455
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.690
456
P MYS005 Myositis 55 0.690
457
MLR026 Miliaria Crystallina 22 0.690
458
MLR009 Miliaria 33 0.690
459
GLC106 Glucocorticoid Resistance, Generalized 47 0.690
460
NWB001 Newborn Respiratory Distress Syndrome 56 0.690
461
c BPL002 Bipolar I Disorder 47 0.690
462
MLR001 Miliaria Rubra 32 0.690
463
P INF037 Inflammatory Bowel Disease 53 0.679
464
P RHM011 Rheumatoid Arthritis 81 0.679
465
OBS002 Obsessive-Compulsive Disorder 67 0.679
466
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.679
467
SPC010 Speech and Communication Disorders 47 0.679
468
HYP001 Hypochromic Microcytic Anemia 36 0.679
469
IGR001 Ige Responsiveness, Atopic 58 0.679
470
PRP016 Paraplegia 52 0.679
471
c HPT016 Hepatitis B 62 0.679
472
P OPT009 Optic Neuritis 57 0.679
473
P CTR002 Cataract 59 0.679
474
DBT010 Diabetic Neuropathy 54 0.679
475
VSC002 Vascular Dementia 59 0.679
476
CLS016 Clostridium Difficile Colitis 49 0.663
477
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 51 0.663
478
P MDL005 Medulloblastoma 75 0.663
479
BRK010 Burkitt Lymphoma 65 0.663
480
P URN019 Urinary Tract Infection 48 0.663
481
P ADL010 Adult Respiratory Distress Syndrome 70 0.663
482
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.663
483
ALC009 Alcoholic Liver Cirrhosis 54 0.663
484
P HML002 Hemolytic Anemia 62 0.663
485
c INH020 Inherited Metabolic Disorder 47 0.663
486
SPL018 Splenomegaly 47 0.663
487
ARG002 Argininosuccinic Aciduria 61 0.656
488
CTR172 Citrullinemia, Classic 64 0.656
489
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.656
490
ACT088 Acute Insulin Response 39 0.656
491
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.656
492
BLP051 Blepharophimosis-Impaired Intellectual Development Syndrome 21 0.656
493
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.656
494
P TTR001 Tetralogy of Fallot 69 0.656
495
PGM029 Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked 50 0.656
496
c INF145 Infantile Liver Failure Syndrome 1 44 0.656
497
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.656
498
ADL002 Adult Syndrome 69 0.656
499
P KHL003 Kohlschutter-Tonz Syndrome 57 0.656
500
P INT099 Intrahepatic Cholestasis of Pregnancy 61 0.656
501
P EPD003 Epidermolysis Bullosa Simplex 56 0.656
502
P HYP750 Hypertriglyceridemia, Familial 61 0.645
503
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 35 0.645
504
CHL065 Cholangiocarcinoma 57 0.645
505
P SDR002 Siderosis 42 0.645
506
INT079 Intrahepatic Cholangiocarcinoma 51 0.645
507
RTN003 Retinal Ischemia 48 0.645
508
P HML001 Hemolytic-Uremic Syndrome 52 0.645
509
PLR008 Pleurisy 49 0.645
510
c BCT007 Bacterial Meningitis 55 0.645
511
ARG004 Argyria 26 0.645
512
WTH001 Withdrawal Disorder 47 0.626
513
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.626
514
P HMN038 Human Coronavirus Sensitivity 30 0.626
515
c PRD040 Periodontitis, Chronic 52 0.626
516
HSH003 Hashimoto Thyroiditis 60 0.626
517
SLC006 Silicosis 55 0.626
518
ANT011 Antisocial Personality Disorder 47 0.626
519
CNV002 Conversion Disorder 47 0.626
520
P PYL005 Pyelonephritis 56 0.626
521
P CNJ013 Conjunctivitis 66 0.626
522
FCL012 Facial Paralysis 49 0.626
523
P TRT010 Teratoma 50 0.626
524
CRY005 Cryptococcosis 61 0.626
525
P RTN018 Retinal Disease 53 0.626
526
ALL006 Allergic Asthma 55 0.626
527
ANP008 Anaplastic Oligoastrocytoma 31 0.626
528
ETN001 Eating Disorder 59 0.626
529
P HYP098 Hypereosinophilic Syndrome 66 0.626
530
P THL005 Thalassemia 56 0.626
531
c ERL012 Early-Onset Glaucoma 23 0.626
532
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.626
533
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.626
534
PLY100 Polyploidy 36 0.626
535
PDT048 Pediatric-Onset Glaucoma of Genetic Origin 11 0.626
536
P CRB088 Cerebral Atrophy 32 0.626
537
SXL003 Sexual Disorder 49 0.605
538
P RTN024 Retinoblastoma 72 0.605
539
c SPN225 Spondyloarthropathy 1 70 0.605
540
SCK003 Sickle Cell Anemia 74 0.605
541
ANG054 Angina Pectoris 65 0.605
542
MSC007 Muscle Hypertrophy 64 0.605
543
KRT019 Keratitis, Hereditary 66 0.605
544
P DNG005 Dengue Virus 55 0.605
545
CLR108 Colorectal Adenoma 63 0.605
546
HYP060 Hyperinsulinism 53 0.605
547
SPN051 Spondylitis 51 0.605
548
KLB003 Klebsiella Pneumonia 49 0.605
549
PNC129 Pancreatic Adenocarcinoma 64 0.605
550
PLR007 Pleural Empyema 50 0.605
551
P CHR012 Chronic Granulomatous Disease 69 0.605
552
ASP003 Aseptic Meningitis 50 0.605
553
CHG001 Chagas Disease 65 0.605
554
ALC010 Alcoholic Cardiomyopathy 42 0.605
555
INF009 Inflammatory Spondylopathy 30 0.605
556
PLC008 Placenta Disease 48 0.605
557
P NRF002 Neurofibromatosis 60 0.605
558
BBS001 Babesiosis 48 0.605
559
P MSC003 Muscular Atrophy 52 0.605
560
OVR094 Ovarian Epithelial Cancer 39 0.605
561
ADG002 Audiogenic Seizures 25 0.605
562
PRS063 Paresthesia 39 0.605
563
PRM329 Premature Aging 36 0.605
564
DRM046 Dermal Ridges-off-the-End 20 0.600
565
STT041 Stuttering 52 0.580
566
MTB004 Metabolic Acidosis 48 0.580
567
ATR057 Atrioventricular Block 54 0.580
568
c MGR028 Migraine with or Without Aura 1 63 0.580
569
DFN341 Deafness, Unilateral 24 0.580
570
LYM133 Lymphoma, Hodgkin, Classic 69 0.580
571
WST001 West Syndrome 64 0.580
572
ANN002 Anencephaly 57 0.580
573
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.580
574
CHD004 Chudley-Mccullough Syndrome 47 0.580
575
KRN002 Kearns-Sayre Syndrome 62 0.580
576
MLG157 Malignant Pheochromocytoma 37 0.580
577
LMB062 Limb Ischemia 55 0.580
578
PRT019 Protein-Losing Enteropathy 44 0.580
579
PPL002 Papillary Carcinoma 46 0.580
580
P LPS002 Liposarcoma 64 0.580
581
BRN014 Bronchopneumonia 52 0.580
582
EXC002 Exocrine Pancreatic Insufficiency 42 0.580
583
CHL147 Chlamydia Pneumonia 47 0.580
584
BTT017 Beta-Thalassemia Major 54 0.580
585
PLM001 Pulmonary Tuberculosis 69 0.580
586
P AGG001 Aggressive Periodontitis 55 0.580
587
P RBL001 Rubella 58 0.580
588
MDS022 Mediastinitis 47 0.580
589
VRL011 Viral Infectious Disease 60 0.580
590
DGN001 Degenerative Disc Disease 48 0.580
591
TNS014 Tenosynovitis 45 0.580
592
P BLR006 Biliary Tract Disease 46 0.580
593
MSL001 Measles 61 0.580
594
CND006 Candida Glabrata 29 0.580
595
ESN002 Eosinophilia-Myalgia Syndrome 40 0.580
596
CCN002 Cocaine Abuse 49 0.580
597
P ALP008 Alopecia 53 0.580
598
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.580
599
GRW007 Growth Hormone Deficiency 47 0.580
600
P AVS003 Avascular Necrosis 41 0.580
601
FNG016 Fungal Keratitis 40 0.580
602
P NJM001 Nijmegen Breakage Syndrome 75 0.559
603
VTM033 Vitamin K Deficiency Bleeding 49 0.559
604
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.552
605
c HMC035 Hemochromatosis, Type 4 52 0.552
606
LGH007 Leigh Syndrome 70 0.552
607
CRD223 Cardiac Arrhythmia 63 0.552
608
TBC004 Tobacco Addiction 63 0.552
609
P GLC113 Galactosemia I 65 0.552
610
P MCH002 Machado-Joseph Disease 62 0.552
611
INT304 Interstitial Pneumonitis, Desquamative, Familial 42 0.552
612
c SPN403 Spinocerebellar Ataxia, X-Linked 2 21 0.552
613
BLC012 Bile Acid Malabsorption, Primary 45 0.552
614
VLV047 Volvulus of Midgut 55 0.552
615
c PLY136 Polydactyly, Preaxial I 32 0.552
616
P LPR021 Leprosy 3 71 0.552
617
FRN006 Frontotemporal Dementia 68 0.552
618
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.552
619
P STR020 Strabismus 56 0.552
620
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.552
621
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 52 0.552
622
c BTT014 Beta-Thalassemia 72 0.552
623
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.552
624
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.552
625
CHR005 Chorioamnionitis 50 0.552
626
LTX001 Latex Allergy 41 0.552
627
PRD003 Periodontosis 25 0.552
628
TTH006 Tooth Disease 51 0.552
629
DRG002 Drug-Induced Hepatitis 42 0.552
630
c BSL007 Basal Cell Carcinoma 67 0.552
631
MST004 Mast Cell Neoplasm 41 0.552
632
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.552
633
FLL031 Follicular Adenoma 40 0.552
634
LPT001 Leptospirosis 65 0.552
635
CRB033 Cerebral Degeneration 36 0.552
636
P OBS001 Obstructive Jaundice 49 0.552
637
ART004 Aortic Atherosclerosis 46 0.552
638
SYN007 Synovitis 54 0.552
639
PRS042 Prostate Disease 42 0.552
640
MTS001 Mutism 44 0.552
641
NTL004 Nut Allergy 38 0.552
642
MYF001 Myofibroma 42 0.552
643
P PTT006 Pituitary Adenoma 55 0.552
644
EXT007 Extracutaneous Mastocytoma 38 0.552
645
PLC002 Plica Syndrome 35 0.552
646
OST011 Osteomalacia 52 0.552
647
P CHR071 Charcot-Marie-Tooth Disease 64 0.552
648
ALL009 Allergic Conjunctivitis 51 0.552
649
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.552
650
LMY002 Leiomyoma 51 0.552
651
PLR022 Pleural Disease 45 0.552
652
CMM004 Common Variable Immunodeficiency 71 0.552
653
GST040 Gastric Adenocarcinoma 66 0.552
654
ACQ007 Acquired Immunodeficiency Syndrome 58 0.552
655
c LCL006 Localized Scleroderma 64 0.552
656
MCH006 Mechanical Strabismus 40 0.552
657
CRV002 Cervix Uteri Carcinoma in Situ 48 0.552
658
PPT005 Peptic Ulcer Disease 58 0.552
659
HNS001 Hansen's Disease 32 0.552
660
P INS002 in Situ Carcinoma 52 0.552
662
BCK006 Back Pain 43 0.552
663
CRV045 Cervical Intraepithelial Neoplasia 38 0.552
664
CRN311 Coronary Ostial Stenosis or Atresia 18 0.552
665
WBR001 Weber Syndrome 38 0.552
666
LKP003 Leukoplakia 39 0.552
667
DYS073 Dysphagia 53 0.552
668
PSR001 Psoriatic Arthritis 61 0.514
669
c FBR070 Febrile Seizures, Familial, 8 44 0.514
670
c SPS097 Spastic Paraplegia 13, Autosomal Dominant 42 0.514
671
DCT002 Ductal Carcinoma in Situ 58 0.514
672
BLR028 Biliary Atresia, Extrahepatic 36 0.514
673
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.514
674
MCK005 Mckusick-Kaufman Syndrome 61 0.514
675
PTN004 Patent Ductus Venosus 31 0.514
676
c PRG019 Paragangliomas 2 30 0.514
677
IMM140 Immunodeficiency 47 56 0.514
678
c NNN034 Noonan Syndrome 12 27 0.514
679
c MJR006 Major Affective Disorder 5 32 0.514
680
MYP120 Myopathy, Distal, with Rimmed Vacuoles 34 0.514
681
CTS011 Cutis Marmorata Telangiectatica Congenita 34 0.514
682
c TBR025 Tuberous Sclerosis 1 84 0.514
683
MYL013 Myeloperoxidase Deficiency 44 0.514
684
IMM162 Immunoglobulin E Concentration, Serum 28 0.514
685
INC002 Inclusion Body Myositis 56 0.514
686
FRB001 Farber Lipogranulomatosis 57 0.514
687
c MJR003 Major Affective Disorder 6 32 0.514
688
P MYS079 Miyoshi Muscular Dystrophy 53 0.514
689
c CHR711 Chronic Asthma 41 0.514
690
LMB024 Limbic Encephalitis 43 0.514
691
ALL007 Allergic Urticaria 27 0.514
692
P CYS018 Cystitis 58 0.514
693
VLV032 Vulva Cancer 60 0.514
694
PRC003 Proctitis 49 0.514
695
c HRD010 Hereditary Spastic Paraplegia 65 0.514
696
ANP005 Anaplastic Astrocytoma 59 0.514
697
P TBR001 Tuberous Sclerosis 69 0.514
698
STR103 Streptococcus Pneumonia 47 0.514
699
NRT001 Neurotic Disorder 56 0.514
700
SMN007 Seminoma 42 0.514
701
MCL006 Macular Retinal Edema 56 0.514
702
CLR030 Clear Cell Renal Cell Carcinoma 53 0.514
703
RCT015 Reactive Arthritis 60 0.514
704
P ACN011 Acne 55 0.514
705
NRM005 Neuromuscular Disease 62 0.514
706
P SYP003 Syphilis 59 0.514
707
MRS001 Marasmus 41 0.514
708
TNS005 Tonsillitis 57 0.514
709
TXC004 Toxic Diffuse Goiter 24 0.514
710
P MTH007 Methemoglobinemia 46 0.514
711
PRV004 Periventricular Leukomalacia 52 0.514
712
P END046 Endometritis 46 0.514
713
P DRM010 Dermatomyositis 61 0.514
714
NRN001 Neuroendocrine Carcinoma 47 0.514
715
IRD001 Iridocyclitis 54 0.514
716
VNZ002 Venezuelan Equine Encephalitis 45 0.514
717
SNL007 Senile Cataract 40 0.514
718
DBT006 Diabetic Macular Edema 48 0.514
719
CHR066 Chronic Fatigue Syndrome 59 0.514
720
P NGH001 Night Blindness 52 0.514
721
PTH003 Pathologic Nystagmus 52 0.514
722
RDT001 Radiation Cystitis 31 0.514
723
GRN017 Granulocytopenia 42 0.514
724
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.514
725
LYM043 Lymphocytic Hypophysitis 31 0.514
726
PYT001 Pythiosis 19 0.514
727
c SPS023 Spastic Paraplegia 13 21 0.514
728
P ALP009 Alopecia Areata 59 0.514
729
LTH004 Lathyrism 15 0.514
730
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 18 0.514
731
LWG005 Low-Grade Astrocytoma 38 0.514
732
CYN003 Cyanide Poisoning 22 0.514
733
RYN005 Raynaud Phenomenon 45 0.514
734
ACT162 Acute Sensory Ataxic Neuropathy 24 0.514
735
NNS011 Nonseminomatous Germ Cell Tumor 32 0.514
736
IDP091 Idiopathic Nephrotic Syndrome 49 0.514
737
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 13 0.514
738
DSR072 Disorder of Energy Metabolism 10 0.514
739
OST062 Osteoarthritis with Mild Chondrodysplasia 46 0.469
740
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.469
741
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.469
742
TND004 Tendinopathy 45 0.469
743
TND005 Tendinitis 53 0.469
744
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 0.469
745
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.469
746
BWN001 Bowen-Conradi Syndrome 54 0.469
747
HYP781 Hypoascorbemia 52 0.469
748
PLY105 Polycystic Ovary Syndrome 1 39 0.469
749
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.469
750
c BLD140 Blood Group, I System 47 0.469
751
ANT039 Antisynthetase Syndrome 55 0.469
752
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.469
753
TRG001 Trigonitis 37 0.469
754
ANS025 Anus Benign Neoplasm 28 0.469
755
MYF002 Myofascial Pain Syndrome 46 0.469
756
MXD026 Mixed Glioma 45 0.469
757
P INT143 Interstitial Cystitis 59 0.469
758
ANS011 Anus Cancer 55 0.469
759
HNT002 Hantavirus Pulmonary Syndrome 55 0.469
760
URT014 Ureterolithiasis 42 0.469
761
ATX019 Ataxia with Vitamin E Deficiency 44 0.469
762
P VSC018 Visceral Steatosis 32 0.469
763
CNT060 Central Serous Chorioretinopathy 38 0.469
764
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.469
765
CHL079 Children's Interstitial Lung Disease 25 0.469
766
MYL020 Myelomeningocele 51 0.424
767
ESN015 Eosinophilic Fasciitis 46 0.424
768
c LBR004 Leber Congenital Amaurosis 1 53 0.424
769
46X083 46,xy Gonadal Dysgenesis with Minifascicular Neuropathy 34 0.424
770
SLF014 Sulfite Oxidase Deficiency, Isolated 53 0.424
771
AML013 Amelogenesis Imperfecta, Hypomaturation Type, Iia1 24 0.424
772
c EPL200 Epilepsy, Childhood Absence 1 30 0.424
773
MSL005 Mseleni Joint Disease 21 0.424
774
GST019 Gastrointestinal Stromal Tumor 78 0.424
775
c VRL012 Viral Meningitis 46 0.424
776
CRB025 Carbohydrate Metabolic Disorder 41 0.424
777
OCC001 Occupational Dermatitis 27 0.424
778
VST003 Vestibular Nystagmus 25 0.424
779
GNR004 Generalized Anxiety Disorder 54 0.424
780
P PNC025 Panic Disorder 52 0.424
781
MYS001 Myositis Ossificans 44 0.424
782
MXD005 Mixed Connective Tissue Disease 57 0.424
783
SPT002 Septicemic Plague 32 0.424
784
P LCH002 Lichen Planus 54 0.424
785
FSC004 Fasciitis 49 0.424
786
PST021 Postpartum Depression 50 0.424
787
RNL012 Renal Tuberculosis 32 0.424
788
LPD009 Lipid Storage Disease 45 0.424
789
ORL013 Oral Lichen Planus 45 0.424
790
DSC009 Discoid Lupus Erythematosus 42 0.424
791
CRD137 Cardiogenic Shock 56 0.424
792
P AST005 Asthma 75 0.361
793
URT010 Ureteral Obstruction 44 0.350
794
P MYC033 Myoclonus 46 0.338
795
P SCL018 Scoliosis 57 0.326
796
PRT251 Proteinuria, Chronic Benign 58 0.326
797
P ECL001 Eclampsia 52 0.326
798
VCC001 Vaccinia 49 0.299
799
DSS032 Disease by Infectious Agent 55 0.286
800
PRP083 Porphyria, Acute Intermittent 64 0.286
801
PHN003 Phenylketonuria 76 0.286
802
c GLL024 Gallbladder Disease 1 53 0.286
803
MTL005 Metal Allergy 40 0.286
804
RTN020 Retinal Vascular Disease 45 0.286
805
MYC005 Myocardial Stunning 45 0.286
806
P CRD119 Cardiac Arrest 68 0.271
807
P SLP006 Sleep Apnea 69 0.271
808
c GLC092 Glaucoma, Primary Open Angle 60 0.271
809
P KLZ004 Kala-Azar 1 41 0.271
810
P BND020 Bone Disease 60 0.271
811
LSH001 Leishmaniasis 63 0.271
812
ORL011 Oral Cancer 60 0.271
813
SPS057 Spasticity 43 0.271
814
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.255
815
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.255
816
P OPN001 Open-Angle Glaucoma 55 0.255
817
CHL004 Cholelithiasis 48 0.255
818
ASP007 Aspiration Pneumonia 49 0.239
819
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.239
820
SNL009 Senile Plaque Formation 28 0.239
821
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.239
822
SYN063 Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction 32 0.239
823
c PRS114 Prostate Cancer, Hereditary, 2 33 0.239
824
P GLM007 Glomerulonephritis 59 0.239
825
SCH014 Schistosomiasis 56 0.239
826
P LCT001 Lactic Acidosis 50 0.239
827
STN013 Stenotrophomonas Maltophilia Infection 26 0.239
828
VRC005 Varicose Veins 59 0.221
829
HND015 Hand Skill, Relative 29 0.221
830
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.221
831
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 55 0.221
832
DFF005 Diffuse Large B-Cell Lymphoma 55 0.221
833
KSH001 Keshan Disease 31 0.221
834
PRT038 Protein-Energy Malnutrition 53 0.221
835
c ACT073 Acute Leukemia 59 0.221
836
P ART005 Arteriovenous Malformation 64 0.221
837
THY029 Thyroid Carcinoma 55 0.221
838
IDP070 Idiopathic Scoliosis 41 0.202
839
c DYS162 Dystonia, Juvenile-Onset 31 0.202
840
ACR006 Aceruloplasminemia 63 0.202
841
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.202
842
LPM012 Lipomatosis, Multiple 59 0.202
843
HMC014 Homocysteinemia 52 0.202
844
ANR007 Anorexia Nervosa 59 0.202
845
P LKM071 Leukemia, Chronic Lymphocytic 74 0.202
846
PLM005 Pleomorphic Lipoma 39 0.202
847
NRL005 Neurilemmoma 60 0.202
848
P LKD001 Leukodystrophy 58 0.202
849
CMM005 Common Cold 55 0.202
850
CRB039 Cerebrovascular Disease 65 0.202
851
P MST002 Mast-Cell Leukemia 50 0.202
852
BNT001 Banti's Syndrome 21 0.202
853
CLF001 Cleft Lip 54 0.202
854
HMP009 Haemophilus Influenzae 41 0.202
855
CHR178 Chromosomal Triplication 33 0.202
856
CRT033 Corticobasal Degeneration 48 0.202
857
MLR004 Malaria 77 0.181
858
c MJR022 Major Affective Disorder 8 37 0.181
859
ALL003 Allergic Rhinitis 66 0.181
860
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.181
861
CYS001 Cystic Fibrosis 77 0.181
862
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.181
863
MNK001 Menkes Disease 64 0.181
864
INS024 Insulin-Like Growth Factor I 77 0.181
865
c MJR024 Major Affective Disorder 9 40 0.181
866
MST021 Meester-Loeys Syndrome 37 0.181
867
P LKM062 Leukemia, Acute Lymphoblastic 69 0.181
868
c OPT053 Optic Atrophy 1 62 0.181
869
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.181
870
END057 Endometrial Cancer 76 0.181
871
P MLT008 Multinodular Goiter 41 0.181
872
OST017 Osteomyelitis 63 0.181
873
PST028 Post-Traumatic Stress Disorder 58 0.181
874
CLN015 Colon Adenocarcinoma 64 0.181
875
P BPL003 Bipolar Disorder 56 0.181
876
NRR001 Neuroretinitis 42 0.181
877
P EHL001 Ehlers-Danlos Syndrome 57 0.181
878
NWC001 Newcastle Disease 47 0.181
879
P AGM001 Agammaglobulinemia 67 0.181
880
ACR005 Acrodermatitis 38 0.181
881
CRN036 Craniopharyngioma 63 0.181
882
GNG013 Gingivitis 59 0.181
883
ART016 Aortic Aneurysm 68 0.181
884
GST033 Gestational Diabetes 60 0.181
885
JPN002 Japanese Encephalitis 61 0.181
886
NPH003 Nephrocalcinosis 49 0.181
887
DYS015 Dysentery 49 0.181
888
RTN023 Retinitis 45 0.181
889
ANT024 Anthrax Disease 57 0.181
890
FSC002 Fascioliasis 43 0.181
891
BSL008 Basal Ganglia Disease 41 0.181
892
KLD004 Keloid Disorder 38 0.181
893
P BRN022 Bronchiectasis 59 0.181
894
P MLG056 Malignant Hyperthermia 65 0.181
895
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.181
896
c LKM005 Leukemia, T-Cell, Chronic 33 0.181
897
ENT007 Enteropathica 25 0.181
898
P PRV006 Pervasive Developmental Disorder 52 0.156
899
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.156
900
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.156
901
EXF001 Exfoliation Syndrome 55 0.156
902
c SCL052 Scleroderma, Familial Progressive 60 0.156
903
P SCL057 Scoliosis, Isolated 1 40 0.156
904
HYP457 Hypertrophic Scars 42 0.156
905
P RST001 Restless Legs Syndrome 52 0.156
906
P EXN002 Exanthem 58 0.156
907
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.156
908
P RTN008 Retinitis Pigmentosa 79 0.156
909
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.156
910
P MMB011 Membranous Nephropathy 50 0.156
911
c LKM063 Leukemia, Chronic Myeloid 70 0.156
912
LPT014 Leptin Deficiency or Dysfunction 77 0.156
913
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.156
914
c PNC108 Pancreatitis, Hereditary 68 0.156
915
OBS082 Obstructive Nephropathy 41 0.156
916
P CRB045 Cerebellar Hypoplasia 40 0.156
917
c ATM099 Autoimmune Uveitis 44 0.156
918
P SLV026 Salivary Gland Carcinoma 59 0.156
919
TRY001 Trypanosomiasis 50 0.156
920
THY128 Thyroid Tumor 33 0.156
921
P RCT021 Rectum Cancer 54 0.156
922
HPT081 Hepatic Infarction 32 0.156
923
MYL001 Myelitis 49 0.156
924
P OLG002 Oligodendroglioma 66 0.156
925
P CYS017 Cystic Teratoma 41 0.156
926
WRN003 Wernicke Encephalopathy 45 0.156
927
MTR010 Mature Teratoma 40 0.156
928
P CND004 Candidiasis 57 0.156
929
HYP006 Hypertensive Heart Disease 48 0.156
930
MDD018 Middle East Respiratory Syndrome 44 0.156
931
c ATM022 Autoimmune Myocarditis 35 0.156
932
ACT098 Acute Erythroid Leukemia 55 0.156
933
CRV040 Cervix Carcinoma 50 0.156
934
PRS021 Prostatic Adenoma 43 0.156
935
GLS001 Gliosarcoma 63 0.156
936
c ACT068 Acute Cystitis 60 0.156
937
P HYD006 Hydrocephalus 62 0.156
938
PRS045 Prostatic Hypertrophy 53 0.156
939
c BNG093 Benign Teratoma 39 0.156
940
TNG007 Tongue Carcinoma 55 0.156
941
P THR014 Thrombocytopenia 66 0.156
942
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.156
943
LKS001 Leukostasis 40 0.156
944
CRB008 Cerebral Atherosclerosis 45 0.156
945
GT001 Gout 63 0.156
946
CHL056 Cheilitis 46 0.156
947
ACT084 Acute Stress Disorder 53 0.156
948
THL004 Theileriasis 26 0.156
949
BRS051 Breast Disease 58 0.156
950
OST016 Osteochondrosis 52 0.156
951
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.156
952
MTC004 Mitochondrial Encephalomyopathy 42 0.156
953
VSC003 Visceral Leishmaniasis 54 0.156
954
PRT036 Peritonitis 65 0.156
955
P