Search results for Manganese

1393 hits were found for Manganese

# Family MCID Name MIFTS Score
1
MNG007 Manganese Poisoning 28 40.235
2
P PRK039 Parkinsonism 55 17.260
3
P HYP821 Hypermanganesemia with Dystonia 26 12.949
4
DSR032 Disorder of Manganese Transport 7 11.635
5
IRN002 Iron Metabolism Disease 57 10.402
6
HPT019 Hepatic Encephalopathy 59 10.193
7
P ENC018 Encephalopathy 62 9.948
8
P TRM003 Tremor 48 9.883
9
HPT004 Hepatic Coma 43 9.277
10
P PRK057 Parkinson Disease, Late-Onset 80 8.966
11
P DYS154 Dystonia 64 8.822
12
CHL068 Cholestasis 61 8.522
13
RPD005 Rapidly Involuting Congenital Hemangioma 46 8.433
14
P LVR013 Liver Disease 69 7.416
15
P NRB001 Neuroblastoma 66 7.348
16
P LTR001 Lateral Sclerosis 58 7.109
17
c AMY091 Amyotrophic Lateral Sclerosis 1 88 7.039
18
HYP266 Hypoxia 57 6.196
19
P MVM001 Movement Disease 61 6.150
20
P HNT016 Huntington Disease 73 6.042
21
P PRN023 Prion Disease 60 5.968
22
P RRH023 Rare Hereditary Hemochromatosis 54 5.919
23
HMS001 Hemosiderosis 48 5.919
24
48X005 48,xyyy 39 5.817
25
LVR012 Liver Cirrhosis 63 5.700
26
AGN016 Aging 54 5.697
27
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 5.692
28
ISC004 Ischemia 61 5.353
29
c ATR087 Atrial Standstill 1 74 5.224
30
P ATT013 Attention Deficit-Hyperactivity Disorder 64 5.024
31
P PHC003 Pheochromocytoma 69 4.936
32
ADR040 Adrenal Gland Pheochromocytoma 46 4.936
33
c HYP716 Hypermanganesemia with Dystonia 1 34 4.910
34
c HMC039 Hemochromatosis, Type 1 73 4.677
35
c DLT002 Dilated Cardiomyopathy 78 4.542
36
P SZR006 Seizure Disorder 70 4.450
37
HLX001 Helix Syndrome 48 4.440
38
P ALZ034 Alzheimer Disease 87 4.419
39
DYS031 Dystonia/parkinsonism, Hypermanganesemia, Polycythemia, and Chronic Liver Disease 14 4.418
40
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.315
41
P PNC035 Pancreatic Cancer 86 4.286
42
GLL048 Glial Tumor 52 4.256
43
GLM045 Glioma 63 4.256
44
HRW001 Hair Whorl 35 4.242
45
SCR011 Scrapie 39 4.197
46
P PLY018 Polycythemia 56 4.190
47
P GLM040 Glioma Susceptibility 1 71 4.158
48
GLB002 Glioblastoma 67 4.035
49
c CNG498 Congenital Disorder of Glycosylation, Type Iin 40 4.005
50
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.942
51
CRB004 Cerebral Artery Occlusion 45 3.928
52
c HYP713 Hypermanganesemia with Dystonia 2 34 3.898
53
NTR005 Nutritional Deficiency Disease 61 3.878
54
DFC004 Deficiency Anemia 74 3.860
55
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.851
56
DRM006 Dermatitis 62 3.838
57
PPL052 Papillomatosis, Confluent and Reticulated 34 3.822
58
HYP066 Hyperglycemia 61 3.794
59
P ESP024 Esophagitis 60 3.781
60
P HYP086 Hypothyroidism 69 3.759
61
P EPL164 Epilepsy 68 3.719
62
KFR001 Kufor-Rakeb Syndrome 59 3.715
63
MLG169 Malignant Astrocytoma 57 3.697
64
SQM006 Squamous Cell Carcinoma 60 3.681
65
P OVR042 Ovarian Cancer 88 3.644
66
47X002 47,xyy 48 3.616
67
P PNM006 Pneumoconiosis 55 3.604
68
ANT018 Anthracosis 51 3.604
69
FTT001 Fatty Liver Disease 62 3.596
70
P ATS364 Autism 69 3.589
71
SLC035 Slc39a14 Deficiency 8 3.567
72
CHL123 Chlamydia 58 3.534
73
P LNG032 Lung Cancer 98 3.533
74
c ATS007 Autism Spectrum Disorder 72 3.512
75
P BNG032 Benign Mesothelioma 53 3.433
76
PSD088 Pseudobulbar Affect 33 3.429
77
BRN071 Brain Injury 50 3.420
78
P BCL017 B-Cell Lymphoma 59 3.402
79
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.377
80
DPH001 Diphtheria 59 3.372
81
TLN003 Telangiectasis 51 3.360
82
c CNT035 Central Nervous System Disease 54 3.330
83
P BRS047 Breast Cancer 98 3.319
84
P PNC044 Pancreatitis 61 3.277
85
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 3.258
86
c TYP009 Type 2 Diabetes Mellitus 92 3.255
87
c TYP008 Type 1 Diabetes Mellitus 70 3.246
88
c MCR115 Microvascular Complications of Diabetes 5 65 3.227
89
ESP021 Esophageal Cancer 83 3.206
90
P FBR017 Fibrosarcoma 56 3.206
91
GTR002 Goiter 53 3.206
92
c CNG411 Congenital Disorder of Glycosylation, Type in 67 3.200
93
ANX004 Anoxia 40 3.199
94
P END033 Endocarditis 58 3.191
95
BRN024 Bronchitis 67 3.176
96
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.172
97
HVY002 Heavy Metal Poisoning 22 3.170
98
OCL069 Ocular Motor Apraxia 57 3.108
99
P DRM053 Dermatitis, Atopic 65 3.104
100
URM002 Uremia 47 3.099
101
DNT012 Dental Caries 53 3.076
102
BNR002 Bone Resorption Disease 47 3.070
103
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 3.055
104
P ATX030 Ataxia-Telangiectasia 80 3.044
105
P HPT021 Hepatitis 69 3.036
106
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.031
107
TRM010 Traumatic Brain Injury 51 3.018
108
P SCH015 Schizophrenia 74 3.012
109
c MCR130 Microvascular Complications of Diabetes 6 41 3.012
110
PRT037 Pertussis 65 3.012
111
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 3.005
112
CHR073 Choreatic Disease 54 3.005
113
CNT047 Contact Dermatitis 57 2.998
114
BRN004 Brain Edema 54 2.986
115
P MLT020 Multiple Sclerosis 79 2.981
116
c PRC016 Pre-Eclampsia 65 2.957
117
P LNG064 Lung Cancer Susceptibility 3 70 2.945
118
ANX010 Anxiety 70 2.933
119
P ADN016 Adenocarcinoma 63 2.922
120
c MCR120 Microvascular Complications of Diabetes 7 47 2.910
121
c MCR113 Microvascular Complications of Diabetes 3 52 2.910
122
c MCR133 Microvascular Complications of Diabetes 4 41 2.910
123
TRD006 Tardive Dyskinesia 53 2.909
124
ADN018 Adenoma 59 2.897
126
SVR001 Severe Acute Respiratory Syndrome 67 2.865
127
CLT003 Colitis 63 2.849
128
SVR004 Severe Combined Immunodeficiency 72 2.840
129
INF034 Infective Endocarditis 54 2.820
130
HDN002 Head Injury 44 2.820
131
LYM017 Lyme Disease 62 2.803
132
c ACT134 Acute Liver Failure 59 2.785
133
CYT002 Cytokine Deficiency 43 2.768
134
HMN044 Human Immunodeficiency Virus Type 1 78 2.766
135
LNG099 Lung Disease 62 2.755
136
BLR001 Biliary Atresia 55 2.749
137
CRT072 Creutzfeldt-Jakob Disease 68 2.741
138
STT001 Status Epilepticus 59 2.728
139
SPN186 Spinal Cord Injury 61 2.711
140
MNN028 Mononeuropathy of the Median Nerve, Mild 46 2.711
141
NPH018 Nephrogenic Systemic Fibrosis 49 2.689
142
LPD008 Lipid Metabolism Disorder 62 2.650
143
NNL006 Non-Alcoholic Steatohepatitis 54 2.645
144
WLS001 Wilson Disease 70 2.642
145
P SHR001 Short Bowel Syndrome 53 2.642
146
c MST023 Mesothelioma, Malignant 56 2.638
147
ENT011 Enterocolitis 55 2.623
148
STM007 Stomatitis 54 2.623
149
P MYC007 Myocardial Infarction 70 2.616
150
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 2.599
151
P TMP001 Temporal Lobe Epilepsy 49 2.576
152
P MLN008 Melanoma 76 2.559
153
RCK004 Rickets 68 2.556
154
P FRD001 Friedreich Ataxia 61 2.538
155
P MTR014 Motor Neuron Disease 65 2.538
156
MLD018 Mild Cognitive Impairment 48 2.536
157
c ACT027 Acute Pancreatitis 60 2.525
158
DWN001 Down Syndrome 70 2.511
159
HGH043 High Grade Glioma 45 2.506
160
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.500
161
P ASP006 Aspergillosis 72 2.500
162
c PCH010 Pachyonychia Congenita 3 43 2.478
163
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.465
164
P HYP069 Hyperparathyroidism 62 2.464
165
P PRD008 Periodontitis 64 2.463
166
DMP001 Dumping Syndrome 43 2.463
167
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.459
168
P NRV007 Nervous System Disease 67 2.459
169
P HPT023 Hepatocellular Carcinoma 96 2.452
170
P HYP061 Hypertrophic Cardiomyopathy 69 2.448
171
P SKN015 Skin Carcinoma 71 2.433
172
ALC007 Alcohol Dependence 66 2.433
173
c SCN007 Secondary Hyperparathyroidism 51 2.432
174
P PRP019 Peripheral Nervous System Disease 58 2.425
175
P NRP001 Neuropathy 60 2.402
176
KRT009 Keratosis 53 2.400
177
TXC002 Toxic Encephalopathy 52 2.398
178
MCS002 Mucositis 56 2.390
179
P INF037 Inflammatory Bowel Disease 53 2.386
180
P GST053 Gastric Cancer 83 2.385
181
P PLY011 Polycystic Ovary Syndrome 57 2.381
182
CRH001 Crohn's Disease 80 2.377
183
P DBT009 Diabetes Mellitus 67 2.376
184
IRN001 Iron Deficiency Anemia 58 2.376
185
OST012 Osteoarthritis 77 2.369
186
P PSR002 Psoriasis 63 2.368
187
PST011 Pustulosis of Palm and Sole 52 2.368
188
P PLM036 Pulmonary Fibrosis 66 2.346
189
DWR001 Dwarfism 44 2.342
190
BRR014 Barrett Esophagus 66 2.333
191
P PLY019 Polyneuropathy 52 2.333
192
P MSC005 Muscular Dystrophy 67 2.305
193
P SLP005 Sleep Disorder 61 2.305
194
c SML038 Small Cell Cancer of the Lung 69 2.300
195
CHL014 Cholera 62 2.298
196
c HYP836 Hypercholesterolemia, Familial, 1 73 2.295
197
INS001 Insulinoma 59 2.295
198
c CHR684 Chronic Kidney Disease 69 2.290
199
PRM236 Primary Biliary Cholangitis 60 2.285
200
P THY032 Thyroiditis 57 2.284
201
P NRN021 Neuronal Ceroid Lipofuscinosis 65 2.275
202
ATH013 Atherosclerosis Susceptibility 63 2.263
203
PRT013 Portal Hypertension 59 2.252
204
OST159 Osteogenic Sarcoma 66 2.243
205
MNT002 Mental Depression 57 2.243
206
P HRT032 Heart Disease 81 2.222
207
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 2.212
208
P INF032 Infertility 57 2.212
209
P MJR001 Major Depressive Disorder 68 2.211
210
P MRC003 Mercury Poisoning 49 2.209
211
P PRS040 Prostate Cancer 95 2.195
212
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 2.195
213
P SPR120 Supranuclear Palsy, Progressive, 1 69 2.175
214
PST092 Posttransplant Acute Limbic Encephalitis 28 2.175
215
MST005 Mastitis 53 2.175
216
DPR016 Depression 65 2.175
217
P LYM118 Lymphoma 67 2.169
218
THY030 Thyroid Gland Disease 50 2.150
219
PRL019 Prolidase Deficiency 50 2.146
220
P ALC033 Alcohol Use Disorder 61 2.146
221
P CHR345 Chronic Pain 50 2.117
222
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.116
223
HYP056 Hypoglycemia 65 2.116
224
LYM019 Lymphosarcoma 46 2.081
225
EXT034 Extrinsic Allergic Alveolitis 57 2.072
226
P PRC019 Precocious Puberty 47 2.055
227
c PLM121 Pulmonary Hypertension, Primary, 4 28 2.042
228
c ACT075 Acute Myocardial Infarction 56 2.042
229
PSY004 Psychotic Disorder 66 2.042
230
c CNG383 Congenital Disorder of Glycosylation, Type Iik 44 2.041
231
P MLN007 Male Infertility 56 2.041
232
MTH071 Methane Production 25 2.037
233
BRN002 Bronchiolitis 57 2.037
234
c BRN108 Branchiootic Syndrome 1 62 2.036
235
MSC157 Muscular Dystrophy, Duchenne Type 79 2.033
236
P SBS003 Substance Abuse 54 2.033
237
P ENC004 Encephalitis 61 2.033
238
P MYC008 Myocarditis 59 2.026
239
CNG034 Congestive Heart Failure 69 2.022
240
P CLR023 Colorectal Cancer 100 1.996
241
BNG091 Benign Chronic Pemphigus 57 1.986
242
IMM167 Immune Deficiency Disease 78 1.982
243
OCC016 Occupational Asthma 33 1.982
244
P OPT006 Optic Nerve Disease 58 1.982
245
TRN015 Transient Cerebral Ischemia 63 1.982
246
PLG002 Plague 58 1.982
247
LRN003 Learning Disability 49 1.965
248
MLG079 Malignant Pleural Mesothelioma 42 1.965
249
ATM095 Autoimmune Disease 61 1.954
250
RNL077 Renal Fibrosis 46 1.954
251
P EYD002 Eye Disease 57 1.951
252
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.948
253
P MYP004 Myopathy 67 1.948
254
P MTC069 Mitochondrial Disorders 57 1.948
255
ORL015 Oral Squamous Cell Carcinoma 43 1.929
256
BLR008 Bilirubin Metabolic Disorder 57 1.929
257
P RSP003 Respiratory Failure 74 1.929
258
P HYP076 Hyperthyroidism 53 1.929
259
P ART021 Arteriosclerosis 54 1.929
260
P SPP010 Suppressor of Tumorigenicity 3 51 1.928
261
SKN016 Skin Disease 63 1.928
262
MLT157 Multiple System Atrophy 1 69 1.899
263
ULC004 Ulcerative Colitis 74 1.899
264
P GST044 Gastritis 55 1.899
265
IMP005 Impotence 52 1.899
266
P PRS038 Personality Disorder 65 1.889
267
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 1.882
268
P MYC084 Mycobacterium Tuberculosis 1 68 1.873
269
P PLM037 Pulmonary Hypertension 72 1.873
270
c HPT073 Hepatitis C Virus 71 1.873
271
CNG491 Congenital Portosystemic Shunt 17 1.866
272
P AST005 Asthma 76 1.866
273
END086 End Stage Renal Disease 52 1.866
274
ALL029 Allergic Disease 59 1.866
275
P PRP029 Porphyria 60 1.866
276
c HPT003 Hepatitis a 63 1.854
277
P BLD134 Bladder Cancer 79 1.848
278
P RTN016 Retinal Degeneration 52 1.848
279
TTN003 Tetanus 65 1.848
280
CVD001 Covid-19 57 1.830
281
NRL016 Neural Tube Defects 81 1.820
282
CHR028 Chronic Wasting Disease 33 1.820
283
P OVR082 Overgrowth Syndrome 49 1.814
284
PLY150 Polykaryocytosis Inducer 29 1.814
285
CHR100 Chronic Ulcer of Skin 57 1.814
286
P HRP006 Herpes Simplex 65 1.814
287
BRN056 Bronchopulmonary Dysplasia 56 1.814
288
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.813
289
P FNG006 Feingold Syndrome 1 62 1.807
290
ATS010 Autosomal Recessive Disease 42 1.794
291
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.794
292
HLC007 Helicobacter Pylori Infection 67 1.794
293
P SYS005 Systemic Scleroderma 74 1.794
294
PCD001 Pica Disease 38 1.794
295
TXC005 Toxic Shock Syndrome 62 1.794
296
AMN003 Amnestic Disorder 54 1.794
297
PRN019 Perinatal Necrotizing Enterocolitis 60 1.793
298
P OST002 Osteoporosis 76 1.773
299
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.773
300
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.773
301
ACT078 Acute Porphyria 49 1.773
302
MYL069 Myeloma, Multiple 77 1.752
303
END028 Endemic Goiter 41 1.752
304
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.751
305
URL001 Urolithiasis 46 1.739
306
PRR015 Preauricular Fistulae, Congenital 19 1.739
307
P UVT001 Uveitis 57 1.739
308
P VSC007 Vascular Disease 63 1.739
309
NRT004 Neuritis 53 1.739
310
PLM010 Pulmonary Edema 55 1.739
311
P HYP265 Hypotonia 42 1.739
312
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.724
313
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.724
314
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.724
315
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.724
316
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.724
317
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.724
318
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.724
319
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.724
320
MNN043 Meningioma, Familial 79 1.724
321
BCT022 Bacterial Infectious Disease 56 1.724
322
SCR001 Secretory Meningioma 40 1.724
323
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.724
324
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.724
325
SPN021 Spinal Meningioma 50 1.724
326
P DMN002 Dementia 66 1.707
327
CRV035 Cervical Cancer 73 1.687
328
HRN029 Hearing Loss, Noise-Induced 37 1.687
329
PPL022 Papilloma 53 1.687
330
SQM002 Squamous Cell Papilloma 46 1.687
331
P AMY004 Amyloidosis 70 1.680
332
P KDN018 Kidney Disease 72 1.680
333
P CHL066 Cholangitis 52 1.680
334
P RHN004 Rhinitis 57 1.680
335
c ESS001 Essential Tremor 57 1.680
336
c HPT016 Hepatitis B 62 1.680
337
CRV043 Cervical Dystonia 46 1.673
338
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.673
339
P BRS044 Breast Adenocarcinoma 58 1.673
340
NPH009 Nephrolithiasis 54 1.673
341
P NSP012 Nasopharyngeal Carcinoma 61 1.652
342
SPC005 Speech Disorder 45 1.652
343
RHB024 Rhabdomyosarcoma 2 67 1.644
344
OTT002 Otitis Media 71 1.620
345
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 1.620
346
P INF038 Influenza 68 1.620
347
ATN005 Autonomic Dysfunction 46 1.620
348
HYP264 Hypertonia 36 1.620
349
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.618
350
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.618
351
P RHM011 Rheumatoid Arthritis 82 1.618
352
GST092 Gastroesophageal Reflux 61 1.618
353
c HNT004 Huntington Disease-Like 2 52 1.618
354
P CTR002 Cataract 60 1.618
355
P ART022 Arthritis 71 1.618
356
FBR047 Fibromyalgia 58 1.614
357
MRV001 Morvan's Fibrillary Chorea 12 1.592
358
P ANR048 Aniridia 1 64 1.581
359
P CRD246 Cardiovascular System Disease 56 1.570
360
P PNM007 Pneumonia 67 1.567
361
c HNT011 Huntington Disease-Like 3 34 1.564
362
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.564
363
c ACT071 Acute Kidney Failure 60 1.564
364
PRT058 Pure Autonomic Failure 58 1.564
365
c DWL002 Dowling-Degos Disease 1 58 1.552
366
ASB001 Asbestosis 47 1.552
367
ASB003 Asbestos Intoxication 32 1.552
368
c HPT001 Hepatitis C 62 1.552
369
CHL067 Cholecystitis 60 1.552
370
GST045 Gastroenteritis 58 1.552
371
P MNN013 Meningitis 65 1.552
372
BRN032 Brain Glioma 45 1.539
373
TNG009 Tongue Squamous Cell Carcinoma 43 1.539
374
SPN035 Spindle Cell Sarcoma 54 1.539
375
SRC014 Sarcoma 65 1.539
376
MDD011 Mood Disorder 62 1.539
377
PHR003 Pharyngitis 58 1.539
378
KWS001 Kwashiorkor 45 1.539
379
PPT001 Peptic Esophagitis 52 1.539
380
KRT002 Keratomalacia 55 1.517
381
c EXD008 Exudative Vitreoretinopathy 1 71 1.505
382
P SLP006 Sleep Apnea 69 1.505
383
LPP008 Lipoprotein Quantitative Trait Locus 65 1.505
384
GLC003 Glucose Intolerance 54 1.505
385
P KDN017 Kidney Cancer 61 1.505
386
P ALL008 Allergic Bronchopulmonary Aspergillosis 54 1.505
387
GNT167 Genetic Obesity 30 1.481
388
P CRN300 Coronary Heart Disease 1 73 1.481
389
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.481
390
CLR109 Colorectal Adenocarcinoma 50 1.481
392
P LPS004 Lupus Erythematosus 61 1.481
393
CNN005 Connective Tissue Disease 67 1.481
394
P NPH012 Nephrotic Syndrome 60 1.481
396
ART140 Arteries, Anomalies of 53 1.443
397
OBS002 Obsessive-Compulsive Disorder 68 1.443
398
SPC010 Speech and Communication Disorders 48 1.443
399
HYP001 Hypochromic Microcytic Anemia 37 1.443
400
IGR001 Ige Responsiveness, Atopic 59 1.443
401
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.443
402
DBT010 Diabetic Neuropathy 54 1.443
403
PRP016 Paraplegia 52 1.443
404
P OPT009 Optic Neuritis 57 1.443
405
VSC002 Vascular Dementia 60 1.443
406
LNG031 Lung Benign Neoplasm 51 1.432
407
CRD132 Cardiac Conduction Defect 60 1.404
408
RHM034 Rahman Syndrome 37 1.404
409
P FLL037 Follicular Lymphoma 74 1.404
410
P MYP006 Myopia 56 1.404
411
P MYL006 Myeloid Leukemia 61 1.404
412
CMB007 Combined Immunodeficiency 57 1.404
413
ALC006 Alcoholic Hepatitis 61 1.404
414
P DRR001 Diarrhea 55 1.404
415
ALL014 Allergic Encephalomyelitis 34 1.404
416
BRN028 Brain Cancer 74 1.403
417
PRT251 Proteinuria, Chronic Benign 57 1.398
418
URT010 Ureteral Obstruction 45 1.398
419
BRK010 Burkitt Lymphoma 66 1.377
420
P URN019 Urinary Tract Infection 49 1.377
421
CLS016 Clostridium Difficile Colitis 49 1.377
422
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 53 1.377
423
P MDL005 Medulloblastoma 75 1.377
424
P HML002 Hemolytic Anemia 62 1.377
425
ALC009 Alcoholic Liver Cirrhosis 54 1.377
426
c INH020 Inherited Metabolic Disorder 48 1.377
427
P ADL010 Adult Respiratory Distress Syndrome 71 1.377
428
SPL018 Splenomegaly 49 1.377
429
OCL006 Ocular Hypertension 53 1.357
430
THY006 Thymus Lymphoma 27 1.357
431
P MYC033 Myoclonus 47 1.351
432
MTC005 Mitochondrial Metabolism Disease 45 1.319
433
SPP011 Suppression of Tumorigenicity 12 61 1.319
434
STR067 Stroke, Ischemic 80 1.319
435
c SYS001 Systemic Lupus Erythematosus 87 1.319
436
c LKM061 Leukemia, Acute Myeloid 83 1.319
437
ACT119 Acute Promyelocytic Leukemia 62 1.319
438
c CHL119 Cholangitis, Primary Sclerosing 58 1.319
439
ACT003 Acute Kidney Tubular Necrosis 46 1.319
440
PNM005 Pneumonic Plague 47 1.319
441
ACR007 Acromegaly 70 1.319
442
P SCL009 Sclerosing Cholangitis 48 1.319
443
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.319
444
c BCT007 Bacterial Meningitis 55 1.307
445
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 35 1.307
446
P HYP750 Hypertriglyceridemia, Familial 62 1.307
447
CHL065 Cholangiocarcinoma 58 1.307
448
ARG004 Argyria 26 1.307
449
P HML001 Hemolytic-Uremic Syndrome 52 1.307
450
c VRL010 Viral Hepatitis 53 1.307
451
PLR008 Pleurisy 50 1.307
452
P SDR002 Siderosis 43 1.307
453
RTN003 Retinal Ischemia 49 1.307
454
INT079 Intrahepatic Cholangiocarcinoma 51 1.307
455
P SCL018 Scoliosis 57 1.302
456
P ECL001 Eclampsia 52 1.302
457
CHP002 Chops Syndrome 47 1.242
458
ALL010 Allergic Contact Dermatitis 56 1.242
459
CCC002 Coccidiosis 50 1.242
460
BBN001 Bubonic Plague 40 1.242
461
PLY100 Polyploidy 36 1.229
462
P THL005 Thalassemia 56 1.229
463
WTH001 Withdrawal Disorder 48 1.229
464
HSH003 Hashimoto Thyroiditis 60 1.229
465
c PRD040 Periodontitis, Chronic 52 1.229
466
P HMN038 Human Coronavirus Sensitivity 30 1.229
467
ALL006 Allergic Asthma 56 1.229
468
PDT048 Pediatric-Onset Glaucoma of Genetic Origin 11 1.229
469
P HYP098 Hypereosinophilic Syndrome 66 1.229
470
CNV002 Conversion Disorder 47 1.229
471
SLC006 Silicosis 56 1.229
472
CRY005 Cryptococcosis 60 1.229
473
FCL012 Facial Paralysis 49 1.229
474
ANT011 Antisocial Personality Disorder 47 1.229
475
P PYL005 Pyelonephritis 57 1.229
476
P CNJ013 Conjunctivitis 66 1.229
477
P RTN018 Retinal Disease 53 1.229
478
P TRT010 Teratoma 51 1.229
479
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 1.229
480
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 1.229
481
c ERL012 Early-Onset Glaucoma 24 1.229
482
P CRB088 Cerebral Atrophy 33 1.229
483
ANP008 Anaplastic Oligoastrocytoma 29 1.229
484
ETN001 Eating Disorder 59 1.229
485
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.222
486
LGG001 Legg-Calve-Perthes Disease 60 1.222
487
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.222
488
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.222
489
P SRC025 Sarcoidosis 1 71 1.222
490
P PLY041 Polymyositis 59 1.222
491
P GRV001 Graves' Disease 55 1.222
492
PLM012 Pulmonary Sarcoidosis 53 1.222
493
BRC012 Brucellosis 66 1.222
494
MCR018 Microcytic Anemia 47 1.222
495
P LRY019 Laryngitis 53 1.222
496
P URT039 Urticaria 58 1.222
497
c PLM128 Pulmonary Hypertension, Primary, 2 28 1.206
498
DSS032 Disease by Infectious Agent 55 1.197
499
VCC001 Vaccinia 47 1.197
500
DSS008 Disease of Mental Health 74 1.170
501
c OVR114 Ovarian Cancer 1 59 1.148
502
BLR013 Biliary Tract Cancer 43 1.148
503
c SPN225 Spondyloarthropathy 1 70 1.144
504
ANG054 Angina Pectoris 66 1.144
505
MSC007 Muscle Hypertrophy 64 1.144
506
SXL003 Sexual Disorder 49 1.144
507
CLR108 Colorectal Adenoma 64 1.144
508
KRT019 Keratitis, Hereditary 66 1.144
509
SCK003 Sickle Cell Anemia 74 1.144
510
P RTN024 Retinoblastoma 73 1.144
511
PCK003 Pick Disease of Brain 69 1.144
512
PRM329 Premature Aging 36 1.144
513
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 1.144
514
P MSC003 Muscular Atrophy 52 1.144
515
ADG002 Audiogenic Seizures 25 1.144
516
PNC129 Pancreatic Adenocarcinoma 65 1.144
517
P CHR012 Chronic Granulomatous Disease 69 1.144
518
PLR007 Pleural Empyema 51 1.144
519
SPN051 Spondylitis 51 1.144
520
P DNG005 Dengue Virus 56 1.144
521
ALC010 Alcoholic Cardiomyopathy 42 1.144
522
CHG001 Chagas Disease 66 1.144
523
INF009 Inflammatory Spondylopathy 30 1.144
524
ASP003 Aseptic Meningitis 50 1.144
525
PLC008 Placenta Disease 49 1.144
526
KLB003 Klebsiella Pneumonia 50 1.144
527
HYP060 Hyperinsulinism 54 1.144
528
BBS001 Babesiosis 49 1.144
529
P NRF002 Neurofibromatosis 57 1.144
530
PRS063 Paresthesia 39 1.144
531
OVR094 Ovarian Epithelial Cancer 39 1.144
532
c GLL024 Gallbladder Disease 1 52 1.142
533
PRP083 Porphyria, Acute Intermittent 65 1.142
534
PHN003 Phenylketonuria 76 1.142
535
MTL005 Metal Allergy 40 1.142
536
RTN020 Retinal Vascular Disease 46 1.142
537
MYC005 Myocardial Stunning 46 1.142
538
HYP005 Hypokalemia 55 1.129
539
PFF001 Pfeiffer Syndrome 77 1.108
540
HYP017 Hypophosphatemia 49 1.108
541
c HNT010 Huntington Disease-Like 1 55 1.108
542
PRN009 Paranoid Schizophrenia 49 1.108
543
MYM001 Myoma 54 1.108
544
ALC005 Alcoholic Pancreatitis 38 1.108
545
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 1.108
546
SPS057 Spasticity 42 1.083
547
P KLZ004 Kala-Azar 1 41 1.083
548
c GLC092 Glaucoma, Primary Open Angle 62 1.083
549
LSH001 Leishmaniasis 64 1.083
550
P CRD119 Cardiac Arrest 67 1.083
551
ORL011 Oral Cancer 60 1.083
552
SQM013 Squamous Cell Carcinoma, Head and Neck 73 1.071
553
CRR017 Curry-Jones Syndrome 35 1.071
554
ATN011 Autoinflammation with Infantile Enterocolitis 45 1.071
555
CMR002 Coumarin Resistance 59 1.071
556
BRK012 Broken Heart Syndrome 42 1.071
557
LYM133 Lymphoma, Hodgkin, Classic 74 1.048
558
GRW007 Growth Hormone Deficiency 46 1.048
559
FNG016 Fungal Keratitis 39 1.048
560
P AVS003 Avascular Necrosis 41 1.048
561
ANN002 Anencephaly 57 1.048
562
c MGR028 Migraine with or Without Aura 1 64 1.048
563
MTB004 Metabolic Acidosis 48 1.048
564
ATR057 Atrioventricular Block 54 1.048
565
LMB062 Limb Ischemia 55 1.048
566
WST001 West Syndrome 59 1.048
567
MLG157 Malignant Pheochromocytoma 36 1.048
568
BTT017 Beta-Thalassemia Major 51 1.048
569
KRN002 Kearns-Sayre Syndrome 63 1.048
570
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.048
571
CHD004 Chudley-Mccullough Syndrome 48 1.048
572
DFN341 Deafness, Unilateral 24 1.048
573
STT041 Stuttering 52 1.048
574
PRT019 Protein-Losing Enteropathy 45 1.048
575
DGN001 Degenerative Disc Disease 49 1.048
576
P RBL001 Rubella 58 1.048
577
VRL011 Viral Infectious Disease 61 1.048
578
P ALP008 Alopecia 54 1.048
579
PLM001 Pulmonary Tuberculosis 69 1.048
580
CHL147 Chlamydia Pneumonia 47 1.048
581
BRN014 Bronchopneumonia 53 1.048
582
PPL002 Papillary Carcinoma 46 1.048
583
MDS022 Mediastinitis 47 1.048
584
CCN002 Cocaine Abuse 49 1.048
585
P LPS002 Liposarcoma 64 1.048
586
EXC002 Exocrine Pancreatic Insufficiency 42 1.048
587
P AGG001 Aggressive Periodontitis 55 1.048
588
LNG015 Lingual-Facial-Buccal Dyskinesia 47 1.048
589
ESN002 Eosinophilia-Myalgia Syndrome 40 1.048
590
TNS014 Tenosynovitis 46 1.048
591
P BLR006 Biliary Tract Disease 46 1.048
592
CND006 Candida Glabrata 30 1.048
593
MSL001 Measles 61 1.048
594
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.021
595
P OPN001 Open-Angle Glaucoma 55 1.021
596
CHL004 Cholelithiasis 49 1.021
597
P BND020 Bone Disease 59 1.021
598
P MCR129 Microvascular Complications of Diabetes 1 68 1.020
599
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 1.020
600
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.958
601
P MYS005 Myositis 56 0.958
602
GLC106 Glucocorticoid Resistance, Generalized 48 0.958
603
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.958
604
MLR026 Miliaria Crystallina 21 0.958
605
NWB001 Newborn Respiratory Distress Syndrome 56 0.958
606
MLR009 Miliaria 33 0.958
607
c BPL002 Bipolar I Disorder 47 0.958
608
MLR001 Miliaria Rubra 32 0.958
609
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.955
610
STN013 Stenotrophomonas Maltophilia Infection 26 0.955
611
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.955
612
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.955
613
SYN063 Syndactyly, Mesoaxial Synostotic, with Phalangeal Reduction 33 0.955
614
SNL009 Senile Plaque Formation 29 0.955
615
c PRS114 Prostate Cancer, Hereditary, 2 33 0.955
616
P LCT001 Lactic Acidosis 51 0.955
617
ASP007 Aspiration Pneumonia 49 0.955
618
SCH014 Schistosomiasis 56 0.955
619
P GLM007 Glomerulonephritis 60 0.955
620
CRN311 Coronary Ostial Stenosis or Atresia 19 0.933
621
WBR001 Weber Syndrome 38 0.933
622
P MCH002 Machado-Joseph Disease 62 0.933
623
FRN006 Frontotemporal Dementia 68 0.933
624
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.933
625
CRD223 Cardiac Arrhythmia 63 0.933
626
P LPR021 Leprosy 3 71 0.933
627
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.933
628
VLV047 Volvulus of Midgut 52 0.933
629
c PLY136 Polydactyly, Preaxial I 32 0.933
630
CHR005 Chorioamnionitis 50 0.933
631
c BTT014 Beta-Thalassemia 72 0.933
632
LGH007 Leigh Syndrome 70 0.933
633
c HMC035 Hemochromatosis, Type 4 52 0.933
634
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.933
635
BLC012 Bile Acid Malabsorption, Primary 44 0.933
636
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.933
637
c SPN403 Spinocerebellar Ataxia, X-Linked 2 20 0.933
638
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.933
639
P CRB180 Cerebelloparenchymal Disorder Ii 14 0.933
640
P GLC113 Galactosemia I 66 0.933
641
INT304 Interstitial Pneumonitis, Desquamative, Familial 42 0.933
642
P STR020 Strabismus 56 0.933
643
TBC004 Tobacco Addiction 63 0.933
644
VSC050 Vascular Malformation, Primary Intraosseous 32 0.933
645
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.933
646
LMY002 Leiomyoma 51 0.933
647
LTX001 Latex Allergy 42 0.933
648
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.933
649
EXT007 Extracutaneous Mastocytoma 38 0.933
650
PRS042 Prostate Disease 42 0.933
651
CRV002 Cervix Uteri Carcinoma in Situ 47 0.933
652
MCH006 Mechanical Strabismus 40 0.933
653
PRD003 Periodontosis 25 0.933
654
MST004 Mast Cell Neoplasm 42 0.933
655
P PTT006 Pituitary Adenoma 55 0.933
656
GST040 Gastric Adenocarcinoma 67 0.933
657
MTS001 Mutism 44 0.933
658
FLL031 Follicular Adenoma 40 0.933
659
ACQ007 Acquired Immunodeficiency Syndrome 59 0.933
660
NTL004 Nut Allergy 37 0.933
661
MYF001 Myofibroma 42 0.933
662
PPT005 Peptic Ulcer Disease 58 0.933
663
c LCL006 Localized Scleroderma 65 0.933
664
OST011 Osteomalacia 52 0.933
665
P CHR071 Charcot-Marie-Tooth Disease 64 0.933
666
PLC002 Plica Syndrome 35 0.933
667
CMM004 Common Variable Immunodeficiency 72 0.933
668
c BSL007 Basal Cell Carcinoma 68 0.933
669
DRG002 Drug-Induced Hepatitis 42 0.933
670
TTH006 Tooth Disease 51 0.933
671
ART004 Aortic Atherosclerosis 47 0.933
672
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.933
673
SYN007 Synovitis 55 0.933
674
P OBS001 Obstructive Jaundice 48 0.933
675
ALL009 Allergic Conjunctivitis 51 0.933
676
PLR022 Pleural Disease 45 0.933
677
CRB033 Cerebral Degeneration 39 0.933
678
LPT001 Leptospirosis 66 0.933
679
P INS002 in Situ Carcinoma 53 0.933
680
HNS001 Hansen's Disease 32 0.933
682
BCK006 Back Pain 47 0.933
683
DYS073 Dysphagia 53 0.933
684
CRV045 Cervical Intraepithelial Neoplasia 39 0.933
685
LKP003 Leukoplakia 39 0.933
686
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 56 0.884
687
DFF005 Diffuse Large B-Cell Lymphoma 54 0.884
688
KSH001 Keshan Disease 34 0.884
689
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.884
690
VRC005 Varicose Veins 60 0.884
691
HND015 Hand Skill, Relative 30 0.884
692
THY029 Thyroid Carcinoma 51 0.884
693
c ACT073 Acute Leukemia 58 0.884
694
PRT038 Protein-Energy Malnutrition 53 0.884
695
P NJM001 Nijmegen Breakage Syndrome 76 0.831
696
VTM033 Vitamin K Deficiency Bleeding 48 0.831
697
c DYS162 Dystonia, Juvenile-Onset 31 0.807
698
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.807
699
ANR007 Anorexia Nervosa 60 0.807
700
HMC014 Homocysteinemia 52 0.807
701
LPM012 Lipomatosis, Multiple 60 0.807
702
P LKM071 Leukemia, Chronic Lymphocytic 75 0.807
703
ACR006 Aceruloplasminemia 63 0.807
704
P LKD001 Leukodystrophy 59 0.807
705
P MST002 Mast-Cell Leukemia 50 0.807
706
CLF001 Cleft Lip 53 0.807
707
PLM005 Pleomorphic Lipoma 40 0.807
708
CMM005 Common Cold 56 0.807
709
CRB039 Cerebrovascular Disease 66 0.807
710
NRL005 Neurilemmoma 60 0.807
711
IDP070 Idiopathic Scoliosis 42 0.807
712
BNT001 Banti's Syndrome 21 0.807
713
CRT033 Corticobasal Degeneration 47 0.807
714
HMP009 Haemophilus Influenzae 41 0.807
715
CHR178 Chromosomal Triplication 34 0.807
716
MCK005 Mckusick-Kaufman Syndrome 61 0.783
717
VNZ002 Venezuelan Equine Encephalitis 46 0.783
718
PRN061 Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures 13 0.783
719
CYN003 Cyanide Poisoning 22 0.783
720
c SPS023 Spastic Paraplegia 13 21 0.783
721
DSR072 Disorder of Energy Metabolism 10 0.783
722
IMM140 Immunodeficiency 47 56 0.783
723
PSR001 Psoriatic Arthritis 62 0.783
724
c PRG019 Paragangliomas 2 30 0.783
725
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.783
726
c CHR711 Chronic Asthma 41 0.783
727
LMB024 Limbic Encephalitis 43 0.783
728
PTN004 Patent Ductus Venosus 31 0.783
729
FRB001 Farber Lipogranulomatosis 58 0.783
730
c SPS097 Spastic Paraplegia 13, Autosomal Dominant 41 0.783
731
c MJR006 Major Affective Disorder 5 32 0.783
732
c MJR003 Major Affective Disorder 6 32 0.783
733
BLR028 Biliary Atresia, Extrahepatic 36 0.783
734
CTS011 Cutis Marmorata Telangiectatica Congenita 34 0.783
735
MYL013 Myeloperoxidase Deficiency 44 0.783
736
c TBR025 Tuberous Sclerosis 1 84 0.783
737
IMM162 Immunoglobulin E Concentration, Serum 28 0.783
738
INC002 Inclusion Body Myositis 57 0.783
739
MYP120 Myopathy, Distal, with Rimmed Vacuoles 32 0.783
740
DCT002 Ductal Carcinoma in Situ 58 0.783
741
c FBR070 Febrile Seizures, Familial, 8 44 0.783
742
IRD001 Iridocyclitis 53 0.783
743
DBT006 Diabetic Macular Edema 48 0.783
744
CHR066 Chronic Fatigue Syndrome 60 0.783
745
ACT162 Acute Sensory Ataxic Neuropathy 24 0.783
746
P ALP009 Alopecia Areata 59 0.783
747
LWG005 Low-Grade Astrocytoma 38 0.783
748
IDP091 Idiopathic Nephrotic Syndrome 47 0.783
749
P CYS018 Cystitis 59 0.783
750
NRN001 Neuroendocrine Carcinoma 47 0.783
751
P SYP003 Syphilis 59 0.783
752
P ACN011 Acne 57 0.783
753
NRM005 Neuromuscular Disease 63 0.783
754
SMN007 Seminoma 42 0.783
755
CLR030 Clear Cell Renal Cell Carcinoma 54 0.783
756
P NGH001 Night Blindness 52 0.783
757
P END046 Endometritis 46 0.783
758
P DRM010 Dermatomyositis 61 0.783
759
c NNN034 Noonan Syndrome 12 27 0.783
760
STR103 Streptococcus Pneumonia 47 0.783
761
TNS005 Tonsillitis 57 0.783
762
MRS001 Marasmus 42 0.783
763
VLV032 Vulva Cancer 60 0.783
764
PRV004 Periventricular Leukomalacia 52 0.783
765
c HRD010 Hereditary Spastic Paraplegia 66 0.783
766
P TBR001 Tuberous Sclerosis 69 0.783
767
TXC004 Toxic Diffuse Goiter 23 0.783
768
P MTH007 Methemoglobinemia 46 0.783
769
P MYS079 Miyoshi Muscular Dystrophy 54 0.783
770
ALL007 Allergic Urticaria 28 0.783
771
RCT015 Reactive Arthritis 61 0.783
772
MCL006 Macular Retinal Edema 57 0.783
773
NRT001 Neurotic Disorder 56 0.783
774
RDT001 Radiation Cystitis 31 0.783
775
ANP005 Anaplastic Astrocytoma 57 0.783
776
PRC003 Proctitis 49 0.783
777
SNL007 Senile Cataract 40 0.783
778
CLS031 Classic Galactosemia and Clinical Variant Galactosemia 18 0.783
779
GRN017 Granulocytopenia 42 0.783
780
PTH003 Pathologic Nystagmus 52 0.783
781
LTH004 Lathyrism 15 0.783
782
RYN005 Raynaud Phenomenon 45 0.783
783
LYM043 Lymphocytic Hypophysitis 31 0.783
784
PYT001 Pythiosis 18 0.783
785
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.783
786
NNS011 Nonseminomatous Germ Cell Tumor 33 0.783
787
P PRD037 Periodontal Ehlers-Danlos Syndrome 49 0.783
788
INS024 Insulin-Like Growth Factor I 78 0.722
789
MST021 Meester-Loeys Syndrome 42 0.722
790
ALL003 Allergic Rhinitis 67 0.722
791
MNK001 Menkes Disease 64 0.722
792
END057 Endometrial Cancer 72 0.722
793
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.722
794
CYS001 Cystic Fibrosis 78 0.722
795
P MLT008 Multinodular Goiter 42 0.722
796
MLR004 Malaria 80 0.722
797
c MJR022 Major Affective Disorder 8 38 0.722
798
P LKM062 Leukemia, Acute Lymphoblastic 69 0.722
799
c MJR024 Major Affective Disorder 9 41 0.722
800
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.722
801
NRR001 Neuroretinitis 42 0.722
802
OST017 Osteomyelitis 63 0.722
803
NPH003 Nephrocalcinosis 49 0.722
804
FSC002 Fascioliasis 44 0.722
805
RTN023 Retinitis 46 0.722
806
P MLG056 Malignant Hyperthermia 66 0.722
807
BSL008 Basal Ganglia Disease 41 0.722
808
CRN036 Craniopharyngioma 64 0.722
809
P BPL003 Bipolar Disorder 56 0.722
810
ART016 Aortic Aneurysm 68 0.722
811
ANT024 Anthrax Disease 58 0.722
812
DYS015 Dysentery 50 0.722
813
CLN015 Colon Adenocarcinoma 65 0.722
814
P AGM001 Agammaglobulinemia 68 0.722
815
GST033 Gestational Diabetes 61 0.722
816
JPN002 Japanese Encephalitis 61 0.722
817
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.722
818
GNG013 Gingivitis 59 0.722
819
ACR005 Acrodermatitis 38 0.722
820
NWC001 Newcastle Disease 47 0.722
821
P EHL001 Ehlers-Danlos Syndrome 58 0.722
822
PST028 Post-Traumatic Stress Disorder 59 0.722
823
KLD004 Keloid Disorder 39 0.722
824
P BRN022 Bronchiectasis 60 0.722
825
c LKM005 Leukemia, T-Cell, Chronic 34 0.722
826
ANR040 Aneurysm 61 0.722
827
ENT007 Enteropathica 25 0.722
828
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.659
829
PGM029 Pigmentary Disorder, Reticulate, with Systemic Manifestations, X-Linked 49 0.659
830
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.659
831
ARG002 Argininosuccinic Aciduria 61 0.659
832
ACT088 Acute Insulin Response 39 0.659
833
KHL003 Kohlschutter-Tonz Syndrome 59 0.659
834
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.659
835
CTR172 Citrullinemia, Classic 65 0.659
836
P TTR001 Tetralogy of Fallot 69 0.659
837
ADL002 Adult Syndrome 70 0.659
838
c INF145 Infantile Liver Failure Syndrome 1 43 0.659
839
P EPD003 Epidermolysis Bullosa Simplex 57 0.659
840
P INT099 Intrahepatic Cholestasis of Pregnancy 62 0.659
841
SPN050 Spinocerebellar Degeneration 39 0.625
842
CLF004 Cleft Lip/palate 57 0.625
843
P HRD217 Hereditary Optic Neuropathy 36 0.625
844
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 26 0.625
845
SMT007 Smith-Fineman-Myers Syndrome 32 0.625
846
THY128 Thyroid Tumor 35 0.625
847
c SCL052 Scleroderma, Familial Progressive 61 0.625
848
P RTN008 Retinitis Pigmentosa 80 0.625
849
c OPT053 Optic Atrophy 1 62 0.625
850
c PNC108 Pancreatitis, Hereditary 69 0.625
851
c LKM063 Leukemia, Chronic Myeloid 71 0.625
852
HYP457 Hypertrophic Scars 42 0.625
853
P RST001 Restless Legs Syndrome 52 0.625
854
P EXN002 Exanthem 58 0.625
855
c ATM099 Autoimmune Uveitis 45 0.625
856
c BNG093 Benign Teratoma 39 0.625
857
ACT098 Acute Erythroid Leukemia 55 0.625
858
P PRV006 Pervasive Developmental Disorder 52 0.625
859
P CRB045 Cerebellar Hypoplasia 40 0.625
860
c ATM022 Autoimmune Myocarditis 36 0.625
861
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.625
862
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.625
863
EXF001 Exfoliation Syndrome 56 0.625
864
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.625
865
LPT014 Leptin Deficiency or Dysfunction 78 0.625
866
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.625
867
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.625
868
P SCL057 Scoliosis, Isolated 1 40 0.625
869
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.625
870
P SLV026 Salivary Gland Carcinoma 58 0.625
871
TNG007 Tongue Carcinoma 52 0.625
872
MDD018 Middle East Respiratory Syndrome 44 0.625
873
OBS082 Obstructive Nephropathy 41 0.625
874
VSC003 Visceral Leishmaniasis 55 0.625
875
MTC004 Mitochondrial Encephalomyopathy 42 0.625
876
SML019 Smallpox 55 0.625
877
P THR014 Thrombocytopenia 66 0.625
878
P OLG002 Oligodendroglioma 66 0.625
879
P CND004 Candidiasis 58 0.625
880
THL004 Theileriasis 31 0.625
881
PRT036 Peritonitis 65 0.625
882
ACT084 Acute Stress Disorder 54 0.625
883
MYL001 Myelitis 50 0.625
884
P MMB011 Membranous Nephropathy 50 0.625
885
TRY001 Trypanosomiasis 50 0.625
886
CRB008 Cerebral Atherosclerosis 46 0.625
887
GT001 Gout 64 0.625
888
c ACT068 Acute Cystitis 61 0.625
889
PRS021 Prostatic Adenoma 43 0.625
890
CRV040 Cervix Carcinoma 50 0.625
891
CHL056 Cheilitis 46 0.625
892
GLS001 Gliosarcoma 64 0.625
893
P CYS017 Cystic Teratoma 41 0.625
894
P HYD006 Hydrocephalus 61 0.625
895
PRS045 Prostatic Hypertrophy 53 0.625
896
HYP006 Hypertensive Heart Disease 49 0.625
897
MTR010 Mature Teratoma 40 0.625
898
GST050 Gastrointestinal System Disease 55 0.625
899
OST016 Osteochondrosis 52 0.625
900
WRN003 Wernicke Encephalopathy 46 0.625
901
BRS051 Breast Disease 58 0.625
902
HPT081 Hepatic Infarction 32 0.625
903
P ART005 Arteriovenous Malformation 65 0.625
904
LKS001 Leukostasis 41 0.625
905
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.625
906
P RCT021 Rectum Cancer 54 0.625
907
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.625
908
P SCK005 Sickle Cell Disease 56 0.625
909
P CRB059 Cerebellar Degeneration 36 0.625
910
NNT021 Neonatal Meningitis 22 0.625
911
HYP144 Hyperacusis 23 0.625
912
NNT049 Nontuberculous Mycobacterial Lung Disease 46 0.625
913
DRM046 Dermal Ridges-off-the-End 20 0.597
914
ADR022 Adrenomyeloneuropathy 39 0.511
915
c FML294 Familial Short Qt Syndrome 43 0.511
916
CNG506 Congenital Amyoplasia 27 0.511
917
ACT228 Acute Radiation Syndrome 30 0.511
918
PRS129 Prostatic Hyperplasia, Benign 49 0.511
919
c THY107 Thymoma, Familial 42 0.511
920
ALK013 Alkaptonuria 59 0.511
921
BLM002 Bulimia Nervosa 57 0.511
922
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 45 0.511
923
CLF027 Cleft Palate, Isolated 64 0.511
924
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.511
925
c PSD108 Pseudohypoparathyroidism, Type Ia 65 0.511
926
P CLC063 Celiac Disease 1 66 0.511
927
PRP027 Peripheral Vascular Disease 71 0.511
928
RSP005 Respiratory System Cancer 29 0.511
930
P ANP001 Anaplastic Large Cell Lymphoma 61 0.511
931
FCL022 Focal Dystonia 42 0.511
932
c SHR030 Short Qt Syndrome 44 0.511
933
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.511
934
KSH004 Kashin-Beck Disease 38 0.511
935
ATM100 Autoimmune Optic Neuritis 28 0.511
936
P PLY014 Polycystic Kidney Disease 69 0.511
937
OLG022 Oligoasthenoteratozoospermia 36 0.511
938
THR024 Thrombosis 56 0.511
939
P FTL001 Fetal Alcohol Syndrome 55 0.511
940
VSC053 Visceral Steatosis, Congenital 34 0.511
941
KPS004 Kaposi Sarcoma 77 0.511
942
P SPN301 Spinocerebellar Ataxia 2 59 0.511
943
MCR025 Microhydranencephaly 33 0.511
944
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 0.511
945
HMM004 Hamamy Syndrome 39 0.511
946
KWS002 Kawasaki Disease 65 0.511
947
WST005 West Nile Virus 57 0.511
948
TBL029 Tubulin, Beta 28 0.511
949
OCC006 Occipital Horn Syndrome 54 0.511
950
c LNG109 Lung Cancer Susceptibility 1 26 0.511
951
c HYD064 Hydrocephalus, Congenital, 1 51 0.511
952
PLY001 Polycythemia Vera 69 0.511
953
c HYP595 Hypertension, Essential 85 0.511
954
P MJR007 Major Affective Disorder 1 42 0.511