Search results for Nicotinamide

1552 hits were found for Nicotinamide

# Family MCID Name MIFTS Score
1
HYP066 Hyperglycemia 61 9.554
2
AGN016 Aging 54 8.995
3
P SKN015 Skin Carcinoma 71 8.282
4
NNL005 Non-Alcoholic Fatty Liver Disease 63 8.111
5
P ACN011 Acne 57 7.973
6
FTT001 Fatty Liver Disease 62 7.905
7
P CHR012 Chronic Granulomatous Disease 69 6.970
8
CRB004 Cerebral Artery Occlusion 45 6.943
9
c TYP008 Type 1 Diabetes Mellitus 70 6.650
10
HYP266 Hypoxia 57 6.629
11
c MCR130 Microvascular Complications of Diabetes 6 41 6.492
12
c MCR120 Microvascular Complications of Diabetes 7 47 6.492
13
c MCR113 Microvascular Complications of Diabetes 3 52 6.492
14
c MCR133 Microvascular Complications of Diabetes 4 41 6.492
15
P PLL002 Pellagra 46 6.488
16
LPD008 Lipid Metabolism Disorder 62 6.282
17
P NRP001 Neuropathy 60 6.228
18
P ALZ034 Alzheimer Disease 87 6.164
19
c CHR684 Chronic Kidney Disease 69 6.133
20
HYP025 Hyperphosphatemia 48 5.986
21
c TYP009 Type 2 Diabetes Mellitus 92 5.974
22
P MLN008 Melanoma 76 5.913
23
TRM010 Traumatic Brain Injury 51 5.862
24
ISC004 Ischemia 61 5.849
25
DPH001 Diphtheria 59 5.735
26
P KDN018 Kidney Disease 72 5.656
27
BRN071 Brain Injury 50 5.633
28
GLC003 Glucose Intolerance 54 5.544
29
P VSC007 Vascular Disease 63 5.542
30
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 5.353
31
c PRC016 Pre-Eclampsia 65 5.300
32
P PRP019 Peripheral Nervous System Disease 58 5.206
33
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 5.200
34
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.113
35
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.113
36
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.113
37
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 5.113
38
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 5.113
39
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.113
40
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 5.113
41
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.113
42
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 5.113
43
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 5.084
44
GLB002 Glioblastoma 67 5.060
45
PMP014 Pemphigoid 51 5.053
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 4.973
47
ATH013 Atherosclerosis Susceptibility 63 4.973
48
P MYP004 Myopathy 67 4.907
49
P DBT009 Diabetes Mellitus 67 4.894
50
WLL004 Wallerian Degeneration 38 4.892
51
P BLD134 Bladder Cancer 79 4.868
52
CHL014 Cholera 62 4.822
53
P NRB001 Neuroblastoma 66 4.761
54
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 4.757
55
P LVR013 Liver Disease 69 4.746
56
P PSR002 Psoriasis 63 4.690
57
PST011 Pustulosis of Palm and Sole 52 4.655
58
DBT010 Diabetic Neuropathy 54 4.581
59
BLL006 Bullous Pemphigoid 61 4.529
60
SQM006 Squamous Cell Carcinoma 60 4.512
61
P DRM053 Dermatitis, Atopic 65 4.409
62
P PRK039 Parkinsonism 55 4.409
63
c ATR087 Atrial Standstill 1 74 4.284
64
CNG034 Congestive Heart Failure 69 4.256
65
P LTR001 Lateral Sclerosis 58 4.247
66
RNL114 Renal Cell Carcinoma, Nonpapillary 80 4.237
67
NNL006 Non-Alcoholic Steatohepatitis 54 4.212
68
HMP009 Haemophilus Influenzae 41 4.212
69
c HYP595 Hypertension, Essential 85 4.210
70
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.198
71
P HNT016 Huntington Disease 73 4.179
72
PRT037 Pertussis 65 4.161
73
END086 End Stage Renal Disease 52 4.159
74
HYP056 Hypoglycemia 65 4.139
75
PRT251 Proteinuria, Chronic Benign 57 4.129
76
48X005 48,xyyy 39 4.110
77
STR067 Stroke, Ischemic 80 4.094
78
RPD005 Rapidly Involuting Congenital Hemangioma 46 3.968
79
ART016 Aortic Aneurysm 68 3.937
80
P FRD001 Friedreich Ataxia 61 3.919
81
ANX004 Anoxia 40 3.896
82
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.882
83
SKN016 Skin Disease 63 3.871
84
P CLR023 Colorectal Cancer 100 3.802
85
P INF032 Infertility 57 3.800
86
c HYP836 Hypercholesterolemia, Familial, 1 73 3.769
87
HYP060 Hyperinsulinism 54 3.767
88
ART140 Arteries, Anomalies of 53 3.744
89
P BCL017 B-Cell Lymphoma 59 3.732
90
INT323 Intraocular Pressure Quantitative Trait Locus 64 3.719
91
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 3.717
92
P MYC084 Mycobacterium Tuberculosis 1 68 3.678
93
c SML038 Small Cell Cancer of the Lung 69 3.678
94
c BSL007 Basal Cell Carcinoma 68 3.678
95
P DMN002 Dementia 66 3.656
96
ANR040 Aneurysm 61 3.650
97
MLD018 Mild Cognitive Impairment 48 3.624
98
P LNG032 Lung Cancer 98 3.612
99
P ADL010 Adult Respiratory Distress Syndrome 71 3.542
100
INS001 Insulinoma 59 3.516
101
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.515
102
FML063 Familial Glucocorticoid Deficiency 58 3.476
103
P OVR042 Ovarian Cancer 88 3.476
104
RSC001 Rosacea 55 3.468
105
P SCK005 Sickle Cell Disease 56 3.463
106
P THR014 Thrombocytopenia 66 3.451
107
c LKM061 Leukemia, Acute Myeloid 83 3.450
108
P PLM037 Pulmonary Hypertension 72 3.435
109
P PRK057 Parkinson Disease, Late-Onset 80 3.420
110
P HPT023 Hepatocellular Carcinoma 96 3.399
111
P HRT032 Heart Disease 81 3.338
112
P LCT001 Lactic Acidosis 51 3.337
113
SKN019 Skin Melanoma 71 3.329
114
CYT002 Cytokine Deficiency 43 3.310
115
P LKM002 Leukemia 67 3.276
116
DBT002 Diabetic Autonomic Neuropathy 41 3.272
117
GLM045 Glioma 63 3.252
118
GLL048 Glial Tumor 52 3.227
119
P MYL006 Myeloid Leukemia 61 3.211
120
IMP005 Impotence 52 3.203
121
c MCR115 Microvascular Complications of Diabetes 5 65 3.192
122
HMC014 Homocysteinemia 52 3.154
123
P MTC133 Mitochondrial Myopathy 50 3.123
124
TXC005 Toxic Shock Syndrome 62 3.109
125
P PLY019 Polyneuropathy 52 3.084
127
P PNC035 Pancreatic Cancer 86 3.043
128
P PMP001 Pemphigus 55 3.037
129
LPP008 Lipoprotein Quantitative Trait Locus 65 3.022
130
c SYS001 Systemic Lupus Erythematosus 87 3.006
131
MTC005 Mitochondrial Metabolism Disease 45 2.976
132
DRM006 Dermatitis 62 2.972
133
HLX001 Helix Syndrome 48 2.945
134
P GST053 Gastric Cancer 83 2.912
135
RNL077 Renal Fibrosis 46 2.907
136
c DLT002 Dilated Cardiomyopathy 78 2.867
137
HRT031 Hartnup Disorder 52 2.854
138
P PRS040 Prostate Cancer 95 2.851
139
BRN004 Brain Edema 54 2.846
140
P MTC069 Mitochondrial Disorders 57 2.836
141
P ART022 Arthritis 71 2.830
142
P LPS004 Lupus Erythematosus 61 2.818
143
P EXN002 Exanthem 58 2.814
144
DFC004 Deficiency Anemia 74 2.808
145
ALL014 Allergic Encephalomyelitis 34 2.807
146
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 2.793
147
P ECL001 Eclampsia 52 2.785
148
P PRD008 Periodontitis 64 2.782
149
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.768
150
P RTN016 Retinal Degeneration 52 2.735
151
P ENC018 Encephalopathy 62 2.734
152
CNS004 Constipation 56 2.729
153
ORL015 Oral Squamous Cell Carcinoma 43 2.721
154
P OPT006 Optic Nerve Disease 58 2.717
155
SPN186 Spinal Cord Injury 61 2.700
156
P LKM071 Leukemia, Chronic Lymphocytic 75 2.696
157
P ALC033 Alcohol Use Disorder 61 2.690
158
P PLY011 Polycystic Ovary Syndrome 57 2.690
159
ATM095 Autoimmune Disease 61 2.670
160
ART002 Arts Syndrome 66 2.663
161
P PLM036 Pulmonary Fibrosis 66 2.663
162
P PNC044 Pancreatitis 61 2.663
163
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 2.663
164
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 2.663
165
ALL029 Allergic Disease 59 2.657
166
KRT009 Keratosis 53 2.657
167
P BRS047 Breast Cancer 98 2.649
168
P ATR011 Atrial Fibrillation 66 2.649
169
P MYC007 Myocardial Infarction 70 2.647
170
KRT002 Keratomalacia 55 2.644
171
P MTH007 Methemoglobinemia 46 2.627
172
P ACT008 Actinic Keratosis 54 2.618
173
SVR004 Severe Combined Immunodeficiency 72 2.614
174
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.577
175
P FBR017 Fibrosarcoma 56 2.577
176
P MLT020 Multiple Sclerosis 79 2.545
177
BCT022 Bacterial Infectious Disease 56 2.545
178
ALC007 Alcohol Dependence 66 2.522
179
P HYP069 Hyperparathyroidism 62 2.505
180
OST012 Osteoarthritis 77 2.476
181
P INF037 Inflammatory Bowel Disease 53 2.467
182
P ADN016 Adenocarcinoma 63 2.467
183
P SLP006 Sleep Apnea 69 2.467
184
CRV035 Cervical Cancer 73 2.428
185
P MLN007 Male Infertility 56 2.416
186
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.398
187
P KDN017 Kidney Cancer 61 2.390
188
P LNG064 Lung Cancer Susceptibility 3 70 2.389
189
MCS002 Mucositis 56 2.389
190
P CTN003 Cutaneous Lupus Erythematosus 52 2.363
191
THY029 Thyroid Carcinoma 51 2.356
192
P MSC005 Muscular Dystrophy 67 2.351
193
P KLZ004 Kala-Azar 1 41 2.341
194
LSH001 Leishmaniasis 64 2.341
195
GST033 Gestational Diabetes 61 2.341
196
c MJR022 Major Affective Disorder 8 38 2.323
197
CLT003 Colitis 63 2.323
198
c MJR024 Major Affective Disorder 9 41 2.323
199
P BPL003 Bipolar Disorder 56 2.323
200
P LRY044 Larynx Cancer 54 2.322
201
CVD001 Covid-19 57 2.311
202
c ACT071 Acute Kidney Failure 60 2.303
203
P NRV007 Nervous System Disease 67 2.303
204
c ACT134 Acute Liver Failure 59 2.264
205
P BRS044 Breast Adenocarcinoma 58 2.264
206
c LKM063 Leukemia, Chronic Myeloid 71 2.259
207
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.237
208
P ATS364 Autism 69 2.228
209
P LPR021 Leprosy 3 71 2.224
210
P HYP750 Hypertriglyceridemia, Familial 62 2.224
211
ULC004 Ulcerative Colitis 74 2.224
212
HNS001 Hansen's Disease 32 2.224
213
CLR030 Clear Cell Renal Cell Carcinoma 54 2.220
214
P HML002 Hemolytic Anemia 62 2.210
215
DWN001 Down Syndrome 70 2.207
216
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.204
217
47X002 47,xyy 48 2.204
218
MTC004 Mitochondrial Encephalomyopathy 42 2.204
219
P GRV001 Graves' Disease 55 2.203
220
P LYM118 Lymphoma 67 2.201
221
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 2.182
222
PMP006 Pemphigus Vulgaris, Familial 58 2.174
223
P CYS018 Cystitis 59 2.163
224
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.163
225
ORL011 Oral Cancer 60 2.149
226
c ATS007 Autism Spectrum Disorder 72 2.135
227
NPH009 Nephrolithiasis 54 2.120
228
CHG001 Chagas Disease 66 2.120
229
RTN003 Retinal Ischemia 49 2.120
230
P OPN001 Open-Angle Glaucoma 55 2.115
231
CHR066 Chronic Fatigue Syndrome 60 2.096
232
P MYC008 Myocarditis 59 2.096
233
SCK003 Sickle Cell Anemia 74 2.091
234
P MCR129 Microvascular Complications of Diabetes 1 68 2.091
235
c PCH010 Pachyonychia Congenita 3 43 2.078
236
OST159 Osteogenic Sarcoma 66 2.078
237
SPN035 Spindle Cell Sarcoma 54 2.078
238
SRC014 Sarcoma 65 2.078
239
P BND020 Bone Disease 59 2.076
240
IMM167 Immune Deficiency Disease 78 2.057
241
P DRR001 Diarrhea 55 2.057
242
P SZR006 Seizure Disorder 70 2.041
243
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.041
244
MYL069 Myeloma, Multiple 77 2.036
245
LNG099 Lung Disease 62 2.036
246
c HPT016 Hepatitis B 62 2.036
247
P RHB003 Rhabdomyosarcoma 66 2.030
248
CND006 Candida Glabrata 30 2.030
249
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.028
250
P LKM062 Leukemia, Acute Lymphoblastic 69 2.022
251
CRB039 Cerebrovascular Disease 66 1.992
252
P RHM011 Rheumatoid Arthritis 82 1.983
253
PRP016 Paraplegia 52 1.983
254
NRR001 Neuroretinitis 42 1.983
255
RTN023 Retinitis 46 1.983
256
CCT002 Cicatricial Pemphigoid 53 1.983
257
PRM329 Premature Aging 36 1.975
258
P MSC003 Muscular Atrophy 52 1.975
259
ATS010 Autosomal Recessive Disease 42 1.975
260
KRN002 Kearns-Sayre Syndrome 63 1.942
261
c ACT068 Acute Cystitis 61 1.934
262
GST023 Gastric Ulcer 52 1.934
263
P CTR002 Cataract 60 1.932
264
HYP014 Hyperuricemia 51 1.932
265
c DWL002 Dowling-Degos Disease 1 58 1.930
266
CRH001 Crohn's Disease 80 1.930
267
P ART021 Arteriosclerosis 54 1.930
268
ANX010 Anxiety 70 1.928
269
PRP027 Peripheral Vascular Disease 71 1.910
270
PRP080 Peripheral Artery Disease 54 1.910
271
LSC001 Lesch-Nyhan Syndrome 62 1.884
272
c CNG223 Congenital Methemoglobinemia 39 1.884
273
URT010 Ureteral Obstruction 45 1.884
274
P HYP265 Hypotonia 42 1.884
275
P ATX030 Ataxia-Telangiectasia 80 1.878
276
TLN003 Telangiectasis 51 1.878
277
P MTR014 Motor Neuron Disease 65 1.877
278
P HYP086 Hypothyroidism 69 1.869
279
ATN004 Autonomic Neuropathy 42 1.869
280
P PLY006 Polydactyly 59 1.842
281
HDN002 Head Injury 44 1.841
282
SYS003 Systolic Heart Failure 49 1.839
283
P PRC031 Preeclampsia/eclampsia 1 43 1.836
284
P OVR082 Overgrowth Syndrome 49 1.831
285
LRY018 Laryngeal Squamous Cell Carcinoma 44 1.831
286
PLL014 Pellagra-Like Syndrome 17 1.812
287
P SCH015 Schizophrenia 74 1.808
288
HMN044 Human Immunodeficiency Virus Type 1 78 1.808
289
P HYP076 Hyperthyroidism 53 1.800
290
OST017 Osteomyelitis 63 1.795
291
PLR008 Pleurisy 50 1.795
292
ACT088 Acute Insulin Response 39 1.775
293
c GLC092 Glaucoma, Primary Open Angle 62 1.775
294
CRC021 Carcinosarcoma 64 1.775
295
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.775
296
P CRD246 Cardiovascular System Disease 56 1.751
297
MTB004 Metabolic Acidosis 48 1.747
298
ACT098 Acute Erythroid Leukemia 55 1.747
299
P ASP006 Aspergillosis 72 1.747
300
CHL045 Choline Deficiency Disease 39 1.747
301
RTN020 Retinal Vascular Disease 46 1.747
302
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.742
303
P RHN004 Rhinitis 57 1.742
304
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.734
305
P NSP012 Nasopharyngeal Carcinoma 61 1.717
306
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.717
307
DGN001 Degenerative Disc Disease 49 1.717
308
c SCN007 Secondary Hyperparathyroidism 51 1.717
309
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 1.717
310
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 33 1.709
312
P FTL001 Fetal Alcohol Syndrome 55 1.696
313
P GRF003 Graft-Versus-Host Disease 71 1.696
314
P RTN018 Retinal Disease 53 1.696
315
KHL003 Kohlschutter-Tonz Syndrome 59 1.681
316
c PSR028 Psoriasis 7 43 1.681
317
c PSR017 Psoriasis 2 53 1.681
318
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.681
319
c PSR018 Psoriasis 13 52 1.681
320
c PSR023 Psoriasis 1 52 1.681
321
c PSR032 Psoriasis 11 47 1.681
322
P CRN300 Coronary Heart Disease 1 73 1.681
323
SBC016 Subacute Delirium 43 1.681
324
c MGR028 Migraine with or Without Aura 1 64 1.672
325
NRL016 Neural Tube Defects 81 1.672
326
c DRM040 Dermatitis Herpetiformis, Familial 35 1.656
327
P DRM007 Dermatitis Herpetiformis 54 1.656
328
GRD001 Giardiasis 46 1.656
329
PLR005 Pleuropneumonia 33 1.656
330
PLM010 Pulmonary Edema 55 1.656
331
NTR005 Nutritional Deficiency Disease 61 1.647
332
LNG031 Lung Benign Neoplasm 51 1.647
333
P HRD217 Hereditary Optic Neuropathy 36 1.643
334
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 1.643
335
P RTN008 Retinitis Pigmentosa 80 1.643
336
URM002 Uremia 47 1.643
337
P EPL164 Epilepsy 68 1.643
338
P GST044 Gastritis 55 1.643
339
P MCR010 Microcephaly 60 1.643
340
P PLY014 Polycystic Kidney Disease 69 1.642
341
MSC157 Muscular Dystrophy, Duchenne Type 79 1.642
342
RCK004 Rickets 68 1.633
343
c ACT027 Acute Pancreatitis 60 1.633
344
PLM001 Pulmonary Tuberculosis 69 1.595
345
ACQ007 Acquired Immunodeficiency Syndrome 59 1.595
346
PRM013 Premature Menopause 58 1.595
347
EWN003 Ewing Sarcoma 70 1.590
348
ART004 Aortic Atherosclerosis 47 1.590
349
SPL018 Splenomegaly 49 1.590
350
ANG054 Angina Pectoris 66 1.588
351
HRW001 Hair Whorl 35 1.588
352
SVR001 Severe Acute Respiratory Syndrome 67 1.588
353
PYR009 Pyridoxine Deficiency Anemia 35 1.588
354
P MNC007 Monocytic Leukemia 47 1.588
355
TRY001 Trypanosomiasis 50 1.588
356
P GLM007 Glomerulonephritis 60 1.588
357
RCT020 Rectum Adenocarcinoma 48 1.588
358
P MNN013 Meningitis 65 1.588
359
GTR002 Goiter 53 1.587
360
c JVN010 Juvenile Rheumatoid Arthritis 66 1.587
361
MLR004 Malaria 80 1.583
362
DPR016 Depression 65 1.544
363
P HPT021 Hepatitis 69 1.530
364
ASP026 Asplenia, Isolated Congenital 43 1.529
365
ONC007 Oncocytoma 50 1.529
366
PPL052 Papillomatosis, Confluent and Reticulated 34 1.529
367
HYP017 Hypophosphatemia 49 1.529
368
P URN019 Urinary Tract Infection 49 1.529
369
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.529
370
CHR177 Chromophobe Renal Cell Carcinoma 54 1.529
371
SLP001 Sleeping Sickness 56 1.529
372
P NTR004 Neutropenia 63 1.529
373
HYP043 Hyperandrogenism 48 1.529
374
CLC006 Calcinosis 47 1.529
375
STT001 Status Epilepticus 59 1.529
376
FML091 Familial Tumoral Calcinosis 43 1.529
377
URM005 Uremic Pruritus 45 1.520
378
P VSC011 Vasculitis 61 1.520
379
BRN056 Bronchopulmonary Dysplasia 56 1.520
380
BLD131 Bladder Urothelial Carcinoma 60 1.511
381
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.490
382
RHB024 Rhabdomyosarcoma 2 67 1.490
383
P ANR048 Aniridia 1 64 1.490
384
ACR006 Aceruloplasminemia 63 1.480
385
P ATX024 Ataxia-Oculomotor Apraxia 3 45 1.480
386
LBR036 Leber Plus Disease 66 1.479
387
HPT022 Hepatoblastoma 54 1.479
388
P CRD119 Cardiac Arrest 67 1.479
389
PRT036 Peritonitis 65 1.474
390
P AST005 Asthma 76 1.468
391
P PHC003 Pheochromocytoma 69 1.468
392
CYN002 Cyanosis, Transient Neonatal 43 1.468
393
LGH007 Leigh Syndrome 70 1.468
394
P RRH023 Rare Hereditary Hemochromatosis 54 1.468
395
ADN018 Adenoma 59 1.468
396
OST003 Osteonecrosis 61 1.468
397
HMS001 Hemosiderosis 48 1.468
398
c RNG019 Ring Chromosome 3 19 1.468
399
MNT002 Mental Depression 57 1.448
400
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 61 1.443
401
HRN029 Hearing Loss, Noise-Induced 37 1.443
402
P CTN015 Cutaneous T Cell Lymphoma 48 1.415
403
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 1.415
404
P LCH002 Lichen Planus 54 1.406
405
c GRN062 Granulomatous Disease, Chronic, Autosomal Recessive, 1 46 1.402
406
PHN003 Phenylketonuria 76 1.402
407
P HYP733 Hypercalciuria, Absorptive, 2 45 1.402
408
P CHR071 Charcot-Marie-Tooth Disease 64 1.402
409
TTH006 Tooth Disease 51 1.402
410
VSC002 Vascular Dementia 60 1.402
411
c ACT135 Acute Graft Versus Host Disease 51 1.402
412
IRR002 Irritable Bowel Syndrome 65 1.402
413
FST010 Fasting Hypoglycemia 33 1.402
414
STN013 Stenotrophomonas Maltophilia Infection 26 1.358
415
PMP008 Pemphigus Vegetans 27 1.358
416
CHR074 Choriocarcinoma 46 1.358
417
P CCK001 Cockayne Syndrome 68 1.358
418
AMN003 Amnestic Disorder 54 1.358
419
ENT004 Enthesopathy 51 1.358
420
P INS002 in Situ Carcinoma 53 1.358
421
CYS001 Cystic Fibrosis 78 1.355
422
c HPT001 Hepatitis C 62 1.355
423
NRM005 Neuromuscular Disease 63 1.342
424
VGN023 Vaginitis 56 1.334
425
RCR030 Recurrent Idiopathic Neuroretinitis 11 1.332
426
P MLN069 Melanoma, Uveal 61 1.332
427
c SVR003 Severe Congenital Neutropenia 59 1.332
428
DFF005 Diffuse Large B-Cell Lymphoma 54 1.332
429
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 1.332
430
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 1.332
431
GRN051 Granulomatous Disease, Chronic, X-Linked 57 1.332
432
MST005 Mastitis 53 1.332
433
CHL123 Chlamydia 58 1.332
434
DSS009 Disseminated Intravascular Coagulation 57 1.332
435
P NRF002 Neurofibromatosis 57 1.332
436
c RNG015 Ring Chromosome 2 22 1.332
437
FML035 Familial Hyperlipidemia 55 1.309
438
LYM133 Lymphoma, Hodgkin, Classic 74 1.301
439
LMY002 Leiomyoma 51 1.301
440
PRT038 Protein-Energy Malnutrition 53 1.301
441
BRN024 Bronchitis 67 1.301
442
PLC008 Placenta Disease 49 1.301
443
P GLM040 Glioma Susceptibility 1 71 1.289
444
PSY004 Psychotic Disorder 66 1.289
445
IRN002 Iron Metabolism Disease 57 1.289
446
LYM019 Lymphosarcoma 46 1.289
447
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 35 1.288
448
c SYS043 Systemic Lupus Erythematosus 1 38 1.288
449
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 1.288
450
c BSL024 Basal Cell Carcinoma 1 55 1.288
451
TMR016 Tumor Suppressor Gene on Chromosome 11 28 1.288
452
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 1.288
453
c CHL140 Chilblain Lupus 1 58 1.288
454
ERY029 Erythermalgia, Primary 58 1.288
455
SPR126 Superior Semicircular Canal Dehiscence 41 1.288
456
P PTT014 Pitt-Hopkins Syndrome 64 1.288
457
SKN013 Skin Benign Neoplasm 50 1.288
458
DBT004 Diabetic Polyneuropathy 50 1.288
459
AND005 Androgen Insensitivity Syndrome, Mild 21 1.288
460
c HMG029 Hemoglobin Se Disease 40 1.288
461
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.288
462
c VRT015 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2 19 1.281
463
PLY100 Polyploidy 36 1.255
464
ALL003 Allergic Rhinitis 67 1.255
465
MTH026 Methemoglobinemia Due to Deficiency of Methemoglobin Reductase 35 1.255
466
P CLD001 Cleidocranial Dysplasia 64 1.255
467
CRV002 Cervix Uteri Carcinoma in Situ 47 1.255
468
PNC129 Pancreatic Adenocarcinoma 65 1.255
469
TRN015 Transient Cerebral Ischemia 63 1.255
470
P RNL015 Renal Hypertension 45 1.255
471
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.255
472
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 1.255
473
CRV045 Cervical Intraepithelial Neoplasia 39 1.255
474
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.242
475
PST092 Posttransplant Acute Limbic Encephalitis 28 1.242
476
CHL068 Cholestasis 61 1.242
477
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.219
478
P EYD002 Eye Disease 57 1.219
479
c SCL052 Scleroderma, Familial Progressive 61 1.190
480
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.190
481
SXL003 Sexual Disorder 49 1.185
482
P OBS001 Obstructive Jaundice 48 1.185
483
ALC006 Alcoholic Hepatitis 61 1.178
484
SPC026 Specific Granule Deficiency 1 31 1.171
485
c OPT053 Optic Atrophy 1 62 1.171
486
P FTL069 Fetal Akinesia Deformation Sequence 1 63 1.171
487
HYD038 Hydrops Fetalis, Nonimmune 59 1.171
488
FTL006 Fetal Alcohol Spectrum Disorder 43 1.171
489
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.171
490
HYP114 Hypertensive Nephropathy 36 1.171
491
c HYD046 Hydatidiform Mole, Recurrent, 1 59 1.171
492
GST010 Gestational Trophoblastic Neoplasm 52 1.171
493
P CND004 Candidiasis 58 1.171
494
OVR063 Overnutrition 42 1.171
495
LYM027 Lymphopenia 56 1.171
496
P SNS001 Sensorineural Hearing Loss 59 1.171
497
P SLP005 Sleep Disorder 61 1.171
498
LST001 Listeriosis 59 1.171
499
NNT021 Neonatal Meningitis 22 1.171
500
NTR011 Neutrophil-Specific Granule Deficiency 36 1.171
501
INT002 Intermittent Claudication 61 1.161
502
GLC008 Glucose Metabolism Disease 40 1.161
503
LRY017 Laryngeal Disease 45 1.161
504
P LRY019 Laryngitis 53 1.161
505
MYL005 Myelofibrosis 71 1.152
506
MYF001 Myofibroma 42 1.152
507
FBR047 Fibromyalgia 58 1.152
508
MCL006 Macular Retinal Edema 57 1.152
509
PMP004 Pemphigus Foliaceus 43 1.148
510
BLD044 Bladder Disease 48 1.148
511
NRT004 Neuritis 53 1.148
512
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.142
513
c VRL010 Viral Hepatitis 53 1.142
514
c MCR112 Microvascular Complications of Diabetes 2 42 1.142
515
c HPT073 Hepatitis C Virus 71 1.134
516
c LBR019 Leber Congenital Amaurosis 9 44 1.134
517
DSS032 Disease by Infectious Agent 55 1.134
518
HGH043 High Grade Glioma 45 1.134
519
PRS045 Prostatic Hypertrophy 53 1.134
520
THR024 Thrombosis 56 1.076
521
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.076
522
PRS021 Prostatic Adenoma 43 1.076
523
GLM044 Glomerular Disease 35 1.075
524
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 1.075
525
END057 Endometrial Cancer 72 1.075
526
BRK010 Burkitt Lymphoma 66 1.075
527
P ANP001 Anaplastic Large Cell Lymphoma 61 1.075
528
APP015 Apparent Mineralocorticoid Excess 57 1.075
529
HYD030 Hydroxykynureninuria 27 1.075
530
c TBR025 Tuberous Sclerosis 1 84 1.075
531
ADN011 Adenoid Cystic Carcinoma 68 1.075
532
OBS082 Obstructive Nephropathy 41 1.075
533
CLF001 Cleft Lip 53 1.075
534
VCC001 Vaccinia 47 1.075
535
ANT024 Anthrax Disease 58 1.075
536
AML001 Amelanotic Melanoma 37 1.075
537
SLD003 Sialadenitis 48 1.075
538
NNT012 Neonatal Jaundice 53 1.075
539
P TBR001 Tuberous Sclerosis 69 1.075
540
P PYL005 Pyelonephritis 57 1.075
541
TRC008 Trachoma 53 1.075
542
URN010 Urinary Tract Obstruction 55 1.075
543
MNN017 Mononeuropathy 41 1.075
544
DBT007 Diabetic Cataract 36 1.075
545
HYP080 Hypogonadism 50 1.075
546
KDN013 Kidney Hypertrophy 34 1.075
547
P PRC019 Precocious Puberty 47 1.075
548
MNT001 Mantle Cell Lymphoma 67 1.057
549
P CNJ013 Conjunctivitis 66 1.057
550
CNT047 Contact Dermatitis 57 1.057
551
PST028 Post-Traumatic Stress Disorder 59 1.057
552
PRS129 Prostatic Hyperplasia, Benign 49 1.014
553
INS024 Insulin-Like Growth Factor I 78 1.014
554
c SPR086 Spermatogenic Failure 3 46 1.014
555
c LKM070 Leukemia, Acute Monocytic 56 1.014
556
BNR002 Bone Resorption Disease 47 1.014
557
c BRN108 Branchiootic Syndrome 1 62 1.014
558
P RTN024 Retinoblastoma 73 1.014
559
TST044 Testicular Torsion 45 1.014
560
ESP021 Esophageal Cancer 83 1.014
561
ADR040 Adrenal Gland Pheochromocytoma 46 1.014
562
ALL006 Allergic Asthma 56 1.014
563
P HRP006 Herpes Simplex 65 1.014
564
ADN001 Adenosine Deaminase Deficiency 59 1.014
565
P RSP003 Respiratory Failure 74 1.014
566
LVR012 Liver Cirrhosis 63 1.014
567
ACT200 Acute Monoblastic Leukemia 41 1.014
568
DST006 Diastolic Heart Failure 45 1.014
569
PTT037 Pituitary Tumors 44 1.014
570
ATN005 Autonomic Dysfunction 46 1.014
571
PMP013 Pemphigus Gestationis 19 1.000
572
DYS015 Dysentery 50 1.000
573
PMP002 Pemphigoid Gestationis 38 1.000
574
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.993
575
HYP781 Hypoascorbemia 52 0.981
576
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.961
577
P MJR001 Major Depressive Disorder 68 0.961
578
c HPT003 Hepatitis a 63 0.961
579
P THY032 Thyroiditis 57 0.961
580
ACT084 Acute Stress Disorder 54 0.961
581
HMT002 Hematologic Cancer 61 0.961
582
LYM040 Lymphoblastic Lymphoma 53 0.961
583
BCK006 Back Pain 47 0.961
584
PST021 Postpartum Depression 50 0.961
585
BLL012 Bullous Impetigo 38 0.961
586
P VTR007 Vitreoretinopathy 46 0.961
587
c ACT150 Acute Adrenal Insufficiency 48 0.961
588
MTH071 Methane Production 25 0.961
589
RTN017 Retinal Detachment 60 0.961
590
c GRN063 Granulomatous Disease, Chronic, Autosomal Recessive, 2 39 0.961
591
ATR057 Atrioventricular Block 54 0.961
592
DFN191 Deafness, Congenital Heart Defects, and Posterior Embryotoxon 22 0.961
593
BLD065 Blue Diaper Syndrome 20 0.961
594
OCL069 Ocular Motor Apraxia 57 0.961
595
P TTR001 Tetralogy of Fallot 69 0.961
596
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.961
597
c SPN291 Spinocerebellar Ataxia 7 53 0.961
599
DBT081 Diabetic Encephalopathy 36 0.961
600
P DYS154 Dystonia 64 0.961
601
P PLY017 Polyarteritis Nodosa 60 0.961
602
TRT001 Teratocarcinoma 42 0.961
603
CRV038 Cervical Squamous Cell Carcinoma 58 0.961
604
P PLY018 Polycythemia 56 0.961
605
IMP004 Impetigo 48 0.961
606
P DRM010 Dermatomyositis 61 0.961
607
ALC010 Alcoholic Cardiomyopathy 42 0.961
608
ADR001 Adrenal Rest Tumor 30 0.961
609
PLP001 Pulpitis 48 0.961
610
ORL004 Oral Submucous Fibrosis 56 0.961
611
P LMY004 Leiomyosarcoma 62 0.961
612
P BNG095 Benign Giant Cell Tumor 43 0.961
613
MYT011 Myotonia 39 0.961
614
CRD132 Cardiac Conduction Defect 60 0.949
615
LMB062 Limb Ischemia 55 0.949
616
INV001 Invasive Aspergillosis 49 0.949
617
ENT011 Enterocolitis 55 0.949
618
CHL065 Cholangiocarcinoma 58 0.949
619
P SYS005 Systemic Scleroderma 74 0.949
620
GT001 Gout 64 0.949
621
MLG169 Malignant Astrocytoma 57 0.949
622
INT079 Intrahepatic Cholangiocarcinoma 51 0.949
623
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 0.879
624
c THY107 Thymoma, Familial 42 0.879
625
P OST002 Osteoporosis 76 0.879
626
c EXD008 Exudative Vitreoretinopathy 1 71 0.879
627
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.879
628
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.879
629
HLC007 Helicobacter Pylori Infection 67 0.879
630
c PRD040 Periodontitis, Chronic 52 0.879
631
EPL131 Epilepsy, Pyridoxine-Dependent 45 0.879
632
URT049 Urate Oxidase, Pseudogene 24 0.879
633
MDD018 Middle East Respiratory Syndrome 44 0.879
634
c ACT075 Acute Myocardial Infarction 56 0.879
635
P RNV001 Renovascular Hypertension 49 0.879
636
MLT006 Multidrug-Resistant Tuberculosis 47 0.879
637
BLR008 Bilirubin Metabolic Disorder 57 0.879
638
P BRB001 Beriberi 44 0.879
639
ECH003 Echinococcosis 53 0.879
640
PRT013 Portal Hypertension 59 0.879
641
P CRN026 Corneal Edema 42 0.879
642
P PRN023 Prion Disease 60 0.879
643
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.879
644
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.879
645
P PNM007 Pneumonia 67 0.879
646
CRT015 Carotid Artery Occlusion 45 0.879
647
P THY023 Thymoma 64 0.879
648
MDD011 Mood Disorder 62 0.879
649
LYM021 Lymphadenitis 56 0.879
650
c LKM005 Leukemia, T-Cell, Chronic 34 0.879
651
DYS073 Dysphagia 53 0.879
652
PRN019 Perinatal Necrotizing Enterocolitis 60 0.879
653
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.847
654
c PRM196 Premature Ovarian Failure 1 59 0.847
655
P SRC025 Sarcoidosis 1 71 0.847
656
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.847
657
KHN001 Kuhnt-Junius Degeneration 48 0.847
658
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.847
659
DWR001 Dwarfism 44 0.847
660
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.826
661
GLS018 Glass Syndrome 61 0.826
662
END040 Endogenous Depression 55 0.826
663
NRT001 Neurotic Disorder 56 0.826
664
DMN026 Dementia Pugilistica 27 0.812
665
TTR011 Tetraploidy 43 0.812
666
DRV001 Dravet Syndrome 69 0.812
667
ADR016 Adrenal Cortical Carcinoma 62 0.812
668
PRP036 Peripheral T-Cell Lymphoma 53 0.812
669
c PRM093 Premature Ovarian Failure 7 48 0.812
670
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.812
671
PRT082 Preterm Premature Rupture of the Membranes 57 0.812
672
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.812
673
PLY001 Polycythemia Vera 69 0.812
674
P FLL037 Follicular Lymphoma 74 0.812
675
ARG004 Argyria 26 0.812
676
OCC016 Occupational Asthma 33 0.812
677
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 0.812
678
CTN007 Cutaneous Leishmaniasis 62 0.812
679
LNG030 Lung Adenoma 37 0.812
680
DRM011 Dermatophytosis 52 0.812
681
P SBR004 Seborrheic Dermatitis 44 0.812
682
PRX097 Paroxysmal Dystonia 32 0.812
683
P HYP098 Hypereosinophilic Syndrome 66 0.812
684
ADR004 Adrenal Cortical Adenocarcinoma 38 0.812
685
RTR001 Retrograde Amnesia 41 0.812
686
CMB007 Combined Immunodeficiency 57 0.812
687
ACR007 Acromegaly 70 0.812
688
SNS003 Sensory Peripheral Neuropathy 52 0.812
689
P ESS003 Essential Thrombocythemia 69 0.812
690
MYL031 Myeloproliferative Neoplasm 66 0.812
691
CRB025 Carbohydrate Metabolic Disorder 40 0.812
692
NRD001 Neurodermatitis 39 0.812
693
NCR002 Necrobiosis Lipoidica 38 0.812
694
KLB003 Klebsiella Pneumonia 50 0.812
695
HML018 Homologous Wasting Disease 21 0.812
696
ANC002 Anca-Associated Vasculitis 44 0.812
697
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.802
698
P LFR001 Li-Fraumeni Syndrome 73 0.802
699
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.802
700
SBJ001 Subjective Cognitive Decline 30 0.802
701
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 41 0.802
702
c HYP272 Hypercholesterolemia, Familial, 3 45 0.802
703
ACR041 Acromelic Frontonasal Dysostosis 53 0.802
704
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 0.802
705
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.802
706
PLY105 Polycystic Ovary Syndrome 1 39 0.802
707
c LFR007 Li-Fraumeni Syndrome 2 46 0.802
708
VTR016 Vater/vacterl Association 49 0.802
709
ADL002 Adult Syndrome 70 0.802
710
c HYP724 Hyperlipoproteinemia, Type Iii 67 0.802
711
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.802
712
VCT001 Vacterl Association 47 0.802
713
c INH030 Inherited Retinal Disorder 28 0.802
714
P THL005 Thalassemia 56 0.802
715
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.802
716
PLY150 Polykaryocytosis Inducer 29 0.802
717
c CNG006 Congenital Hypothyroidism 63 0.802
718
P CRP001 Carpal Tunnel Syndrome 66 0.802
719
P HRS035 Hirschsprung Disease 1 66 0.802
720
P SCL018 Scoliosis 57 0.802
722
CRT020 Cortisone Reductase Deficiency 34 0.802
723
FND002 Fundus Dystrophy 55 0.802
724
SLC006 Silicosis 56 0.802
725
P HYP061 Hypertrophic Cardiomyopathy 69 0.802
726
VRC001 Varicocele 48 0.802
727
P NPH012 Nephrotic Syndrome 60 0.802
728
c ATM011 Autoimmune Hepatitis 63 0.802
729
c INH020 Inherited Metabolic Disorder 48 0.802
730
CYS008 Cystic Echinococcosis 57 0.802
731
CYT014 Cytochrome P450 Oxidoreductase Deficiency 34 0.802
732
HYP572 Hypoganglionosis 27 0.802
733
CRB090 Cerebral Hypoxia 42 0.802
735
P MYC033 Myoclonus 47 0.802
736
PRT058 Pure Autonomic Failure 58 0.802
737
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.793
738
c BCT007 Bacterial Meningitis 55 0.717
739
PNM013 Pneumococcal Meningitis 43 0.717
740
SPS057 Spasticity 42 0.717
741
P RTT002 Rett Syndrome 79 0.717
742
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.717
743
TND004 Tendinopathy 45 0.717
744
P ADL017 Adult T-Cell Leukemia 56 0.717
745
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.717
746
MSC007 Muscle Hypertrophy 64 0.717
747
TND005 Tendinitis 54 0.717
748
ART074 Aortic Dissection 53 0.717
749
ANT003 Antley-Bixler Syndrome 49 0.717
750
LKC009 Leukocyte Adhesion Deficiency, Type I 70 0.717
751
CNT105 Central Core Disease of Muscle 59 0.717
752
KPS004 Kaposi Sarcoma 77 0.717
753
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.717
754
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.717
755
ACT119 Acute Promyelocytic Leukemia 62 0.717
756
P SPP010 Suppressor of Tumorigenicity 3 51 0.717
757
c SPN294 Spinocerebellar Ataxia 1 53 0.717
758
CLR109 Colorectal Adenocarcinoma 50 0.717
759
BLP004 Blepharophimosis 36 0.717
760
c PRM340 Primary Adrenal Insufficiency 38 0.717
761
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.717
762
P TRM003 Tremor 48 0.717
763
P HMP002 Hemophagocytic Lymphohistiocytosis 61 0.717
764
CRT013 Carotid Stenosis 51 0.717
765
CLN015 Colon Adenocarcinoma 65 0.717
766
SCH014 Schistosomiasis 56 0.717
767
TRN018 Transitional Cell Carcinoma 56 0.717
768
LYM017 Lyme Disease 62 0.717
769
TTN003 Tetanus 65 0.717
770
P TMP001 Temporal Lobe Epilepsy 49 0.717
771
IRT001 Iritis 45 0.717
772
P AGG001 Aggressive Periodontitis 55 0.717
773
P ICH004 Ichthyosis 56 0.717
774
ADS004 Aids Dementia Complex 40 0.717
775
CRB086 Cerebral Aneurysms 40 0.717
776
RYN005 Raynaud Phenomenon 45 0.717
777
c RNG024 Ring Chromosome 8 28 0.717
778
CRC006 Carcinoid Syndrome 55 0.717
779
c ART115 Aortic Valve Disease 1 74 0.699
780
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.699
781
SMT004 Smith-Lemli-Opitz Syndrome 70 0.699
782
OBS002 Obsessive-Compulsive Disorder 68 0.699
783
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 59 0.699
784
NRL018 Neural Tube Defects, Folate-Sensitive 45 0.699
785
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.699
786
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.699
787
PRD013 Periodic Fever, Familial, Autosomal Dominant 68 0.699
788
APN008 Apnea, Obstructive Sleep 67 0.699
789
MCR004 Macroglobulinemia 49 0.699
790
HYP005 Hypokalemia 55 0.699
791
HMG005 Hemoglobinopathy 56 0.699
792
PRD004 Prediabetes Syndrome 52 0.699
793
THY030 Thyroid Gland Disease 50 0.699
794
c FML021 Familial Hypercholesterolemia 72 0.699
795
CRB037 Cerebral Palsy 67 0.699
796
P HYP121 Hypoalphalipoproteinemia 43 0.699
797
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.658
798
P SCK002 Sick Sinus Syndrome 55 0.641
799
P URT039 Urticaria 58 0.641
800
ART035 Arterial Calcification of Infancy 58 0.624
801
CLC017 Calcification of Joints and Arteries 44 0.624
802
CLD014 Cole Disease 38 0.624
803
24D001 2,4-Dienoyl-Coa Reductase Deficiency 34 0.624
804
PRQ002 Paraquat Poisoning 28 0.621
805
c ACQ047 Acquired Methemoglobinemia 30 0.621
806
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.621
807
P MYS003 Myasthenia Gravis 68 0.621
808
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.621
809
SJG002 Sjogren-Larsson Syndrome 54 0.621
810
PSR001 Psoriatic Arthritis 62 0.621
811
P CLC063 Celiac Disease 1 66 0.621
812
BCT021 Bacterial Sepsis 43 0.621
813
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.621
814
IGR001 Ige Responsiveness, Atopic 59 0.621
815
c DMN005 Diamond-Blackfan Anemia 2 28 0.621
816
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 0.621
817
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.621
818
LPT014 Leptin Deficiency or Dysfunction 78 0.621
819
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.621
820
GLC042 Glucocorticoid Deficiency 1 50 0.621
821
CTR172 Citrullinemia, Classic 65 0.621
822
BTT016 Batten-Turner Congenital Myopathy 53 0.621
823
P MYP087 Myopathy, Tubular Aggregate, 1 49 0.621
824
RBF001 Riboflavin Deficiency 49 0.621
825
PNG002 Pain Agnosia 51 0.621
826
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.621
827
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 0.621
828
ACT003 Acute Kidney Tubular Necrosis 46 0.621
829
P AMY004 Amyloidosis 70 0.621
830
ACH005 Achalasia 55 0.621
831
P MLG056 Malignant Hyperthermia 66 0.621
832
CHC001 Chickenpox 57 0.621
833
IGG001 Iga Glomerulonephritis 50 0.621
834
P CNT004 Centronuclear Myopathy 57 0.621
835
P MMB011 Membranous Nephropathy 50 0.621
836
P UVT001 Uveitis 57 0.621
837
BRN028 Brain Cancer 74 0.621
838
CRN019 Coronary Artery Vasospasm 47 0.621
839
FLR001 Filarial Elephantiasis 59 0.621
840
CRV040 Cervix Carcinoma 50 0.621
841
P GLY013 Glycogen Storage Disease 60 0.621
842
FLR002 Filariasis 55 0.621
843
P END047 Endophthalmitis 53 0.621
844
ALC005 Alcoholic Pancreatitis 38 0.621
845
P INT068 Intestinal Disease 53 0.621
846
GST050 Gastrointestinal System Disease 55 0.621
847
P TRT010 Teratoma 51 0.621
848
ERL001 Early Myoclonic Encephalopathy 62 0.621
849
P TCD001 Tic Disorder 49 0.621
850
P NML001 Nemaline Myopathy 48 0.621
851
OLG001 Oligospermia 45 0.621
852
P PTS002 Ptosis 52 0.621
853
IDP070 Idiopathic Scoliosis 42 0.621
854
P OVR049 Ovarian Disease 52 0.621
855
AZS001 Azoospermia 45 0.621
856
c SVR005 Severe Pre-Eclampsia 50 0.621
857
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.621
858
STM007 Stomatitis 54 0.621
859
P CHR345 Chronic Pain 50 0.621
860
MYC017 Mycobacterium Kansasii 36 0.621
861
ETN001 Eating Disorder 59 0.621
862
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.507
863
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.507
864
CLP005 Ciliopathy 41 0.507
865
MTB016 Metabolic Myopathy 30 0.507
866
STR077 Streptococcal Toxic-Shock Syndrome 35 0.507
867
BNG077 Benign Idiopathic Neonatal Seizures 23 0.507
868
CCN009 Cocaine Intoxication 30 0.507
869
ACT228 Acute Radiation Syndrome 30 0.507
870
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.507
871
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 0.507
872
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.507
873
FRN006 Frontotemporal Dementia 68 0.507
874
CRD223 Cardiac Arrhythmia 63 0.507
875
ANR007 Anorexia Nervosa 60 0.507
876
P MTR004 Maturity-Onset Diabetes of the Young 68 0.507
877
P MYS005 Myositis 56 0.507
878
LNT004 Lentigines 46 0.507
879
CLF027 Cleft Palate, Isolated 64 0.507
880
EPC005 Epicanthus 36 0.507
881
ARY002 Aryl Hydrocarbon Hydroxylase Inducibility 24 0.507
882
GST092 Gastroesophageal Reflux 61 0.507
883
VLV047 Volvulus of Midgut 52 0.507
884
c MST023 Mesothelioma, Malignant 56 0.507
885
c FNC027 Fanconi Anemia, Complementation Group a 81 0.507
886
HYP457 Hypertrophic Scars 42 0.507
887
P BRG001 Brugada Syndrome 69 0.507
888
P PRG013 Paraganglioma 57 0.507
889
HMR023 Hemorrhagic Cystitis 43 0.507
890
MYL009 Myelodysplastic Syndrome 67 0.507
891
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.507
892
CLR108 Colorectal Adenoma 64 0.507
893
c ATM022 Autoimmune Myocarditis 36 0.507
894
P CHN012 Chondrosarcoma 57 0.507
895
WRN002 Wernicke-Korsakoff Syndrome 50 0.507
896
c HYP602 Hyperoxaluria, Primary, Type Ii 49 0.507
897
BSM002 Bosma Arhinia Microphthalmia Syndrome 44 0.507
898
CHD004 Chudley-Mccullough Syndrome 48 0.507
899
P ORT004 Orthostatic Intolerance 63 0.507
900
IMP012 Impdh2 Enzyme Activity, Variation in 8 0.507
901
IMM224 Immunodeficiency 68 36 0.507
902
c LNG109 Lung Cancer Susceptibility 1 26 0.507
903
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 0.507
904
c WLM013 Wilms Tumor 1 66 0.507
905
P SCL057 Scoliosis, Isolated 1 40 0.507
906
GLB001 Gilbert Syndrome 53 0.507
907
MLT157 Multiple System Atrophy 1 69 0.507
908
INC002 Inclusion Body Myositis 57 0.507
909
P MDL005 Medulloblastoma 75 0.507
910
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.507
911
TNG009 Tongue Squamous Cell Carcinoma 43 0.507
912
MTC111 Mitochondrial Neurogastrointestinal Encephalomyopathy 47 0.507
913
P HRD144 Hereditary Mixed Polyposis Syndrome 54 0.507
914
HPT004 Hepatic Coma 43 0.507
915
PRN049 Paraneoplastic Pemphigus 44 0.507
916
FSC002 Fascioliasis 44 0.507
917
CRN030 Coronary Stenosis 50 0.507
918
CHR078 Chorioretinitis 51 0.507
919
GSG001 Gas Gangrene 52 0.507
920
P ATR005 Atrophic Gastritis 50 0.507
921
P PLM034 Pulmonary Emphysema 58 0.507
922
P ALP008 Alopecia 54 0.507
923
ACT168 Acute Annular Outer Retinopathy 10 0.507
924
P ANT006 Antiphospholipid Syndrome 55 0.507
925
PHG002 Phagocyte Bactericidal Dysfunction 34 0.507
926
PNM008 Pneumothorax 54 0.507
927
PLC005 Placental Insufficiency 56 0.507
928
GRN007 Granuloma Annulare 43 0.507
929
FLL031 Follicular Adenoma 40 0.507
930
ILS001 Ileus 50 0.507
931
P INF038 Influenza 68 0.507
932
EPD006 Epidermolysis Bullosa Acquisita 48 0.507
933
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 0.507
934
P VNS003 Venous Insufficiency 55 0.507
935
CRT017 Cartilage Disease 53 0.507
936
PLC002 Plica Syndrome 35 0.507
937
CRN017 Coronary Thrombosis 46 0.507
938
CRY005 Cryptococcosis 60 0.507
939
P ESP024 Esophagitis 60 0.507
940
P OPT009 Optic Neuritis 57 0.507
941
SHG001 Shigellosis 63 0.507
942
LWC001 Low Compliance Bladder 45 0.507
943
HPT019 Hepatic Encephalopathy 59 0.507
944
ALC009 Alcoholic Liver Cirrhosis 54 0.507
945
TST015 Testicular Disease 42 0.507
946
CHR063 Chronic Mucocutaneous Candidiasis 68 0.507
947
P KRN004 Kernicterus 46 0.507
948