Search results for Niacin

866 hits were found for Niacin

# Family MCID Name MIFTS Score
1
P PLL002 Pellagra 46 31.586
2
LPD008 Lipid Metabolism Disorder 62 27.513
3
c HYP836 Hypercholesterolemia, Familial, 1 73 18.021
4
ATH013 Atherosclerosis Susceptibility 63 12.623
5
P HYP750 Hypertriglyceridemia, Familial 62 12.140
6
P CRN300 Coronary Heart Disease 1 73 11.740
7
LPP008 Lipoprotein Quantitative Trait Locus 65 10.289
8
P MYP004 Myopathy 67 10.000
9
ART140 Arteries, Anomalies of 53 9.905
10
c TYP009 Type 2 Diabetes Mellitus 92 8.407
11
PRP027 Peripheral Vascular Disease 71 8.333
12
P VSC007 Vascular Disease 63 8.321
13
ISC004 Ischemia 61 8.278
14
FML035 Familial Hyperlipidemia 55 7.437
15
c HRM017 Hermansky-Pudlak Syndrome 2 55 6.999
16
P SCH015 Schizophrenia 74 6.717
17
P HRT032 Heart Disease 81 6.549
18
HYP025 Hyperphosphatemia 48 6.537
19
FTT001 Fatty Liver Disease 62 6.513
20
P DBT009 Diabetes Mellitus 67 6.407
21
c FML021 Familial Hypercholesterolemia 72 6.047
22
c HNT004 Huntington Disease-Like 2 52 6.007
23
P CRD246 Cardiovascular System Disease 56 5.869
24
NNL005 Non-Alcoholic Fatty Liver Disease 63 5.822
25
c CHR684 Chronic Kidney Disease 69 5.779
26
P KDN018 Kidney Disease 72 5.551
27
P PLM036 Pulmonary Fibrosis 66 5.486
28
END086 End Stage Renal Disease 52 5.413
29
P HYP733 Hypercalciuria, Absorptive, 2 45 5.301
30
EPT021 Epithelial Recurrent Erosion Dystrophy 46 5.243
31
MCL006 Macular Retinal Edema 57 5.174
32
HYP066 Hyperglycemia 61 5.102
33
c HYP272 Hypercholesterolemia, Familial, 3 45 5.070
34
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 5.070
35
48X005 48,xyyy 39 4.901
36
P EXN002 Exanthem 58 4.834
37
P LVR013 Liver Disease 69 4.691
38
P ENC018 Encephalopathy 62 4.650
39
ALC007 Alcohol Dependence 66 4.637
40
CRB039 Cerebrovascular Disease 66 4.630
41
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.572
42
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.572
43
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.572
44
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.572
45
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.572
46
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.572
47
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.572
48
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.572
49
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.572
50
P SKN015 Skin Carcinoma 71 4.555
51
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 4.467
52
PRP080 Peripheral Artery Disease 54 4.415
53
c HNT011 Huntington Disease-Like 3 34 4.410
54
CRN030 Coronary Stenosis 50 4.370
55
P DRR001 Diarrhea 55 4.348
56
P MYC007 Myocardial Infarction 70 4.276
57
PRT037 Pertussis 65 4.258
58
NNL006 Non-Alcoholic Steatohepatitis 54 4.209
59
PSY004 Psychotic Disorder 66 4.074
60
P HYP838 Hyperlipidemia, Familial Combined, 3 61 4.066
61
P MYC084 Mycobacterium Tuberculosis 1 68 4.055
62
HRT031 Hartnup Disorder 52 4.007
63
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.974
64
DFC004 Deficiency Anemia 74 3.944
65
c HYP724 Hyperlipoproteinemia, Type Iii 67 3.937
66
c MJR022 Major Affective Disorder 8 38 3.674
67
c MJR024 Major Affective Disorder 9 41 3.674
68
P BPL003 Bipolar Disorder 56 3.674
69
HPT022 Hepatoblastoma 54 3.667
70
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 3.638
71
INT002 Intermittent Claudication 61 3.504
72
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 3.404
73
HYP081 Hypolipoproteinemia 49 3.385
74
P RTN022 Retinal Vein Occlusion 54 3.383
75
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 3.256
76
ULC004 Ulcerative Colitis 74 3.247
77
MTB004 Metabolic Acidosis 48 3.230
78
CLT003 Colitis 63 3.199
79
P HYP121 Hypoalphalipoproteinemia 43 3.185
80
SCK003 Sickle Cell Anemia 74 3.176
81
END072 Endotheliitis 36 3.153
82
OPD001 Opioid Abuse 44 3.150
83
P NRP001 Neuropathy 60 3.132
84
P PRP019 Peripheral Nervous System Disease 58 3.132
85
HMN044 Human Immunodeficiency Virus Type 1 78 3.114
86
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.095
87
P MYS005 Myositis 56 3.090
88
c ACT027 Acute Pancreatitis 60 3.081
89
IRN002 Iron Metabolism Disease 57 3.081
90
c MCR115 Microvascular Complications of Diabetes 5 65 3.064
91
MNT002 Mental Depression 57 3.062
92
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.043
93
CRT016 Carotid Artery Disease 52 2.986
94
c MGR028 Migraine with or Without Aura 1 64 2.880
95
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.879
96
GLB002 Glioblastoma 67 2.874
97
P SCK005 Sickle Cell Disease 56 2.874
98
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.864
99
RBF001 Riboflavin Deficiency 49 2.859
100
STR067 Stroke, Ischemic 80 2.848
101
HYD030 Hydroxykynureninuria 27 2.847
103
c HYP740 Hyperlipoproteinemia, Type V 53 2.821
104
CNT016 Central Retinal Vein Occlusion 54 2.786
105
NRL016 Neural Tube Defects 81 2.767
106
HYP056 Hypoglycemia 65 2.759
107
CYT002 Cytokine Deficiency 43 2.759
108
c HYP839 Hyperlipidemia, Familial Combined, 1 30 2.756
109
P INF037 Inflammatory Bowel Disease 53 2.741
110
HMC014 Homocysteinemia 52 2.714
111
P PRK039 Parkinsonism 55 2.707
112
PLM001 Pulmonary Tuberculosis 69 2.701
113
P MTC133 Mitochondrial Myopathy 50 2.691
114
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.664
115
CRB004 Cerebral Artery Occlusion 45 2.663
116
HYP014 Hyperuricemia 51 2.653
117
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.644
118
P ANR048 Aniridia 1 64 2.644
119
c ACT134 Acute Liver Failure 59 2.621
120
END040 Endogenous Depression 55 2.610
121
PRT251 Proteinuria, Chronic Benign 57 2.598
122
TRN015 Transient Cerebral Ischemia 63 2.598
123
P PLM037 Pulmonary Hypertension 72 2.593
124
AGN016 Aging 54 2.593
125
PRM013 Premature Menopause 58 2.585
126
P PLY011 Polycystic Ovary Syndrome 57 2.585
127
NRN004 Neuroendocrine Tumor 59 2.554
128
SBC016 Subacute Delirium 43 2.554
129
P ALC033 Alcohol Use Disorder 61 2.553
130
c BLD140 Blood Group, I System 46 2.541
131
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 2.541
132
RSC001 Rosacea 55 2.541
133
GT001 Gout 64 2.540
134
TXC005 Toxic Shock Syndrome 62 2.528
135
P BRB001 Beriberi 44 2.524
136
ACN002 Acanthosis Nigricans 56 2.487
137
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 2.432
138
CRC006 Carcinoid Syndrome 55 2.427
139
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.419
140
P ART021 Arteriosclerosis 54 2.406
141
PPL052 Papillomatosis, Confluent and Reticulated 34 2.374
142
PPT005 Peptic Ulcer Disease 58 2.374
143
KRT002 Keratomalacia 55 2.350
144
ANT039 Antisynthetase Syndrome 55 2.336
145
IMP005 Impotence 52 2.315
146
P PNC044 Pancreatitis 61 2.312
147
P THR014 Thrombocytopenia 66 2.282
148
BRN071 Brain Injury 50 2.253
149
CND006 Candida Glabrata 30 2.253
150
DRM006 Dermatitis 62 2.244
151
CNS004 Constipation 56 2.242
152
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.235
153
P OPN001 Open-Angle Glaucoma 55 2.235
154
DPR016 Depression 65 2.225
155
P MJR007 Major Affective Disorder 1 42 2.223
156
P MYC033 Myoclonus 47 2.217
157
P CTR002 Cataract 60 2.215
158
HYP060 Hyperinsulinism 54 2.215
159
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 2.188
160
PYR009 Pyridoxine Deficiency Anemia 35 2.188
161
P CRD119 Cardiac Arrest 67 2.188
162
ART016 Aortic Aneurysm 68 2.173
163
PRT036 Peritonitis 65 2.173
164
PRT038 Protein-Energy Malnutrition 53 2.173
165
P NRV007 Nervous System Disease 67 2.173
166
P LCT001 Lactic Acidosis 51 2.150
167
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.141
168
HMZ003 Homozygous Familial Hypercholesterolemia 60 2.140
169
HYP555 Hypertriglyceridemia, Transient Infantile 38 2.100
170
P DRM053 Dermatitis, Atopic 65 2.098
171
P CLR023 Colorectal Cancer 100 2.098
172
c BSL007 Basal Cell Carcinoma 68 2.098
173
P INF032 Infertility 57 2.098
174
ANR040 Aneurysm 61 2.098
175
c HYP841 Hypoalphalipoproteinemia, Primary, 1 49 2.086
176
P MJR001 Major Depressive Disorder 68 2.086
177
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.056
178
P HDC001 Headache 57 2.056
179
SPN186 Spinal Cord Injury 61 2.050
180
DRG002 Drug-Induced Hepatitis 42 2.050
181
STM007 Stomatitis 54 2.036
182
NTR005 Nutritional Deficiency Disease 61 2.029
183
P MLN008 Melanoma 76 2.019
184
c ACT071 Acute Kidney Failure 60 2.019
185
NRT001 Neurotic Disorder 56 1.992
186
MYC017 Mycobacterium Kansasii 36 1.976
187
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.969
188
P TRN020 Turner Syndrome 67 1.955
189
c HPT003 Hepatitis a 63 1.953
190
ACQ007 Acquired Immunodeficiency Syndrome 59 1.933
191
P LKM002 Leukemia 67 1.933
192
MST005 Mastitis 53 1.904
193
MDD011 Mood Disorder 62 1.904
194
DBT081 Diabetic Encephalopathy 36 1.883
195
HYP266 Hypoxia 57 1.840
196
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.833
197
HRW001 Hair Whorl 35 1.833
198
P CRT085 Carotid Intimal Medial Thickness 2 22 1.833
199
TRC022 Tricuspid Valve Insufficiency 47 1.833
200
GLS007 Glossitis 47 1.833
201
c INH020 Inherited Metabolic Disorder 48 1.833
202
P HYP086 Hypothyroidism 69 1.788
203
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.758
204
P HYP076 Hyperthyroidism 53 1.758
205
ANR007 Anorexia Nervosa 60 1.747
206
WRN003 Wernicke Encephalopathy 46 1.747
207
P LNG032 Lung Cancer 98 1.737
208
MLR004 Malaria 80 1.737
209
c SML038 Small Cell Cancer of the Lung 69 1.737
210
GLC003 Glucose Intolerance 54 1.721
211
P PRD008 Periodontitis 64 1.717
212
KRT009 Keratosis 53 1.717
213
P URN019 Urinary Tract Infection 49 1.679
214
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.679
215
P HML002 Hemolytic Anemia 62 1.679
216
XRD026 Xeroderma Pigmentosum-Cockayne Syndrome Complex 35 1.679
217
LYM027 Lymphopenia 56 1.679
218
P CCK001 Cockayne Syndrome 68 1.679
219
SLC006 Silicosis 56 1.679
220
c DLT002 Dilated Cardiomyopathy 78 1.679
221
DFC001 Defective Apolipoprotein B-100 24 1.679
222
c MCR130 Microvascular Complications of Diabetes 6 41 1.667
223
c MCR120 Microvascular Complications of Diabetes 7 47 1.667
224
c MCR113 Microvascular Complications of Diabetes 3 52 1.667
225
c MCR133 Microvascular Complications of Diabetes 4 41 1.667
226
P MTC069 Mitochondrial Disorders 57 1.646
227
PMP014 Pemphigoid 51 1.620
228
P PSR002 Psoriasis 63 1.620
229
PST011 Pustulosis of Palm and Sole 52 1.620
230
BLL006 Bullous Pemphigoid 61 1.620
231
PRN011 Pernicious Anemia 53 1.614
232
ACT088 Acute Insulin Response 39 1.593
233
KRT019 Keratitis, Hereditary 66 1.593
234
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.593
235
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.593
236
P ALP008 Alopecia 54 1.593
237
SKN016 Skin Disease 63 1.593
238
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.593
239
P RSP003 Respiratory Failure 74 1.593
240
DSS009 Disseminated Intravascular Coagulation 57 1.593
241
PRP030 Purpura 54 1.593
242
IMM167 Immune Deficiency Disease 78 1.575
243
ANX010 Anxiety 70 1.550
244
c ART101 Aortic Valve Disease 2 66 1.550
245
ASP030 Aspirin Resistance 40 1.500
246
EXP004 Exophthalmos 51 1.500
247
P NTR004 Neutropenia 63 1.500
248
CRN017 Coronary Thrombosis 46 1.500
249
RTN020 Retinal Vascular Disease 46 1.500
250
KWS001 Kwashiorkor 45 1.500
251
FNT004 Fainting 29 1.500
252
CRH001 Crohn's Disease 80 1.495
253
RCK004 Rickets 68 1.495
254
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.469
255
ART002 Arts Syndrome 66 1.469
256
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.469
257
PRD013 Periodic Fever, Familial, Autosomal Dominant 68 1.469
258
P PRK057 Parkinson Disease, Late-Onset 80 1.465
259
KRN002 Kearns-Sayre Syndrome 63 1.465
260
DSS008 Disease of Mental Health 74 1.465
261
CNG034 Congestive Heart Failure 69 1.444
262
c ART115 Aortic Valve Disease 1 74 1.412
263
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.409
264
P ACN011 Acne 57 1.409
265
P PLY019 Polyneuropathy 52 1.409
266
P BRG001 Brugada Syndrome 69 1.397
267
c SCH087 Schizophrenia 18 28 1.397
268
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.397
269
P TRM003 Tremor 48 1.397
270
47X002 47,xyy 48 1.397
271
BRN028 Brain Cancer 74 1.397
272
LVR012 Liver Cirrhosis 63 1.397
273
P SBS003 Substance Abuse 54 1.397
274
DMY004 Demyelinating Disease 50 1.397
275
CHL068 Cholestasis 61 1.397
276
QDR001 Quadriplegia 50 1.397
278
ESP021 Esophageal Cancer 83 1.381
279
AMN006 Aminoaciduria 37 1.381
280
INT007 Intermediate Coronary Syndrome 54 1.358
281
GNG013 Gingivitis 59 1.358
282
P ATS364 Autism 69 1.316
283
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 1.281
284
SMT004 Smith-Lemli-Opitz Syndrome 70 1.281
285
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 1.281
286
P GLM040 Glioma Susceptibility 1 71 1.281
287
ADL002 Adult Syndrome 70 1.281
288
SPR126 Superior Semicircular Canal Dehiscence 41 1.281
289
c HMG029 Hemoglobin Se Disease 40 1.281
290
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.281
291
c SCH051 Schizophrenia 4 32 1.280
292
END057 Endometrial Cancer 72 1.280
293
MYC078 Myoclonus and Ataxia 32 1.280
294
c MYC058 Myocardial Infarction 2 24 1.280
295
c GLC092 Glaucoma, Primary Open Angle 62 1.280
296
HPT004 Hepatic Coma 43 1.280
297
P SBR004 Seborrheic Dermatitis 44 1.280
298
HRD016 Hereditary Retinal Dystrophy 34 1.280
299
ATR073 Atrophic Glossitis 31 1.280
300
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.280
301
HPT019 Hepatic Encephalopathy 59 1.280
302
ALC009 Alcoholic Liver Cirrhosis 54 1.280
303
P DYS005 Dyslexia 41 1.280
304
P PRP029 Porphyria 60 1.280
305
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 1.280
306
P THR117 Three M Syndrome 1 65 1.248
307
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 1.248
308
LPD009 Lipid Storage Disease 45 1.248
309
DWR001 Dwarfism 44 1.248
310
P HNT016 Huntington Disease 73 1.235
311
CRD005 Cardia Cancer 38 1.235
312
P LYM118 Lymphoma 67 1.231
313
P BLD134 Bladder Cancer 79 1.213
314
P LPR021 Leprosy 3 71 1.213
315
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.213
316
c PRC016 Pre-Eclampsia 65 1.213
317
HNS001 Hansen's Disease 32 1.213
318
DSS032 Disease by Infectious Agent 55 1.155
319
THY029 Thyroid Carcinoma 51 1.155
320
P GRV001 Graves' Disease 55 1.155
321
GTR002 Goiter 53 1.155
322
INS024 Insulin-Like Growth Factor I 78 1.141
323
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.141
324
P ACT008 Actinic Keratosis 54 1.141
325
INS001 Insulinoma 59 1.141
326
P SYS005 Systemic Scleroderma 74 1.141
327
SCH014 Schistosomiasis 56 1.141
328
P ICH004 Ichthyosis 56 1.141
329
c ICH023 Ichthyosis, Acquired 30 1.141
330
P MLT020 Multiple Sclerosis 79 1.096
331
HYP005 Hypokalemia 55 1.096
332
P DMN002 Dementia 66 1.096
333
SCL003 Social Phobia 48 1.096
334
CRN027 Corneal Neovascularization 47 1.070
335
PTH003 Pathologic Nystagmus 52 1.070
336
MCL027 Macular Dystrophy, Dominant Cystoid 51 1.028
337
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.028
338
NRR001 Neuroretinitis 42 1.028
339
RTN023 Retinitis 46 1.028
340
SCH003 Schizophreniform Disorder 55 1.028
341
c HYP843 Hypoalphalipoproteinemia, Primary, 2 50 0.982
342
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.982
343
MLD017 Mal De Debarquement Syndrome 29 0.982
344
ATM095 Autoimmune Disease 61 0.976
345
CHP002 Chops Syndrome 47 0.976
346
BLD065 Blue Diaper Syndrome 20 0.976
347
PST092 Posttransplant Acute Limbic Encephalitis 28 0.976
348
FDL002 Food Allergy 47 0.976
349
ASP007 Aspiration Pneumonia 49 0.976
350
CHL004 Cholelithiasis 49 0.976
351
NRT004 Neuritis 53 0.976
352
P PNM007 Pneumonia 67 0.976
353
MCR017 Macrocytic Anemia 44 0.976
354
ORL011 Oral Cancer 60 0.976
355
ETN001 Eating Disorder 59 0.976
356
P VRT014 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 1 23 0.960
357
c VRT015 Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2 19 0.960
358
ENT011 Enterocolitis 55 0.960
359
SCH012 Schizoaffective Disorder 50 0.960
360
P DRM010 Dermatomyositis 61 0.960
361
ART004 Aortic Atherosclerosis 47 0.960
362
TNS014 Tenosynovitis 46 0.960
363
PYR016 Pyridoxine Deficiency 29 0.960
364
MTC005 Mitochondrial Metabolism Disease 45 0.957
365
P ALZ034 Alzheimer Disease 87 0.957
366
CYS001 Cystic Fibrosis 78 0.957
367
HYP781 Hypoascorbemia 52 0.957
368
c ATS007 Autism Spectrum Disorder 72 0.957
369
P HPT023 Hepatocellular Carcinoma 96 0.957
370
SKN019 Skin Melanoma 71 0.957
371
DBT010 Diabetic Neuropathy 54 0.957
372
TLN003 Telangiectasis 51 0.957
373
VTM033 Vitamin K Deficiency Bleeding 48 0.957
374
P EYD002 Eye Disease 57 0.957
375
P LRY019 Laryngitis 53 0.957
376
CRB037 Cerebral Palsy 67 0.957
377
c TYP008 Type 1 Diabetes Mellitus 70 0.873
378
P CLC063 Celiac Disease 1 66 0.873
379
ANG054 Angina Pectoris 66 0.873
380
P HYP768 Hyperlipoproteinemia, Type I 67 0.873
381
WRN002 Wernicke-Korsakoff Syndrome 50 0.873
382
P GST053 Gastric Cancer 83 0.873
383
PHN003 Phenylketonuria 76 0.873
384
P SLP005 Sleep Disorder 61 0.873
385
CRB089 Cerebral Beriberi 19 0.873
386
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.873
387
MYC019 Mycobacterium Marinum 29 0.873
388
c RNG015 Ring Chromosome 2 22 0.873
389
MYC016 Mycobacterium Gordonae 20 0.873
390
BRC012 Brucellosis 66 0.863
391
c HPT016 Hepatitis B 62 0.863
392
c PRM196 Premature Ovarian Failure 1 59 0.826
393
P FNG006 Feingold Syndrome 1 62 0.826
394
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.826
395
c MJR006 Major Affective Disorder 5 32 0.826
396
c MJR023 Major Affective Disorder 7 33 0.826
397
c MJR004 Major Affective Disorder 4 28 0.826
398
c MJR003 Major Affective Disorder 6 32 0.826
399
PLY105 Polycystic Ovary Syndrome 1 39 0.826
400
c MJR008 Major Affective Disorder 2 34 0.826
401
OPT003 Opiate Dependence 49 0.826
402
SYS003 Systolic Heart Failure 49 0.826
403
LYM133 Lymphoma, Hodgkin, Classic 74 0.794
404
KPR003 Keipert Syndrome 44 0.794
405
OBS002 Obsessive-Compulsive Disorder 68 0.794
406
SXL003 Sexual Disorder 49 0.794
407
P MCR129 Microvascular Complications of Diabetes 1 68 0.794
408
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.794
409
RHB024 Rhabdomyosarcoma 2 67 0.794
410
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 54 0.794
411
P PRS038 Personality Disorder 65 0.794
412
ACT084 Acute Stress Disorder 54 0.794
413
c MCR112 Microvascular Complications of Diabetes 2 42 0.794
414
CRB008 Cerebral Atherosclerosis 46 0.794
415
INT074 Intracranial Arteriosclerosis 22 0.794
416
OBS003 Obsessive-Compulsive Personality Disorder 43 0.794
417
VGN023 Vaginitis 56 0.794
418
PST028 Post-Traumatic Stress Disorder 59 0.794
419
AND005 Androgen Insensitivity Syndrome, Mild 21 0.794
420
LYM019 Lymphosarcoma 46 0.794
421
c SYS001 Systemic Lupus Erythematosus 87 0.777
422
P OVR042 Ovarian Cancer 88 0.777
423
c ATR087 Atrial Standstill 1 74 0.777
424
MLD018 Mild Cognitive Impairment 48 0.777
425
P LKM062 Leukemia, Acute Lymphoblastic 69 0.777
426
DWN001 Down Syndrome 70 0.777
427
MYL069 Myeloma, Multiple 77 0.777
428
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.777
429
P LPS004 Lupus Erythematosus 61 0.777
430
P BCL017 B-Cell Lymphoma 59 0.777
431
c HPT001 Hepatitis C 62 0.777
432
c VRL010 Viral Hepatitis 53 0.777
433
BLD131 Bladder Urothelial Carcinoma 60 0.777
434
FBR047 Fibromyalgia 58 0.777
435
OST012 Osteoarthritis 77 0.777
436
P ECL001 Eclampsia 52 0.777
437
HMG005 Hemoglobinopathy 56 0.777
438
BRN024 Bronchitis 67 0.777
439
P CNJ013 Conjunctivitis 66 0.777
440
P RHN004 Rhinitis 57 0.777
441
P ADL010 Adult Respiratory Distress Syndrome 71 0.777
442
SQM006 Squamous Cell Carcinoma 60 0.777
443
HDN002 Head Injury 44 0.777
444
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.756
445
P OVR082 Overgrowth Syndrome 49 0.756
446
PRS129 Prostatic Hyperplasia, Benign 49 0.756
447
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 56 0.756
448
PLY150 Polykaryocytosis Inducer 29 0.756
449
CLF027 Cleft Palate, Isolated 64 0.756
450
P ORF002 Orofacial Cleft 43 0.756
451
EXT033 Extrapulmonary Tuberculosis 45 0.756
452
IGR001 Ige Responsiveness, Atopic 59 0.756
453
IDP093 Idiopathic Gastroparesis 28 0.756
454
P GLL020 Gallbladder Disease 56 0.756
455
SVR001 Severe Acute Respiratory Syndrome 67 0.756
456
P OPT006 Optic Nerve Disease 58 0.756
457
DNT012 Dental Caries 53 0.756
458
PRS021 Prostatic Adenoma 43 0.756
459
P DDN001 Duodenal Ulcer 53 0.756
460
EXS001 Exostosis 49 0.756
461
PRS045 Prostatic Hypertrophy 53 0.756
462
PRM020 Premenstrual Tension 39 0.756
463
ACR005 Acrodermatitis 38 0.756
464
GST037 Gastroparesis 52 0.756
465
HYP141 Hyperphenylalaninemia 42 0.756
466
ENT007 Enteropathica 25 0.756
467
P THL005 Thalassemia 56 0.618
468
RST023 Resting Heart Rate, Variation in 40 0.618
469
c SCL052 Scleroderma, Familial Progressive 61 0.618
470
ANN002 Anencephaly 57 0.618
471
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 0.618
472
VSC044 Visceral Myopathy 50 0.618
473
P OST002 Osteoporosis 76 0.618
474
OTT002 Otitis Media 71 0.618
475
VTM002 Vitamin B12 Deficiency 48 0.618
476
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.618
477
c BTT014 Beta-Thalassemia 72 0.618
478
BTN004 Biotin Deficiency 45 0.618
479
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.618
480
BNR002 Bone Resorption Disease 47 0.618
481
HLC007 Helicobacter Pylori Infection 67 0.618
482
P PNC035 Pancreatic Cancer 86 0.618
483
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.618
484
P HYP058 Hypervitaminosis a 47 0.618
485
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.618
486
SCH011 Schizotypal Personality Disorder 36 0.618
487
PRP005 Parapsoriasis 38 0.618
488
P MSC003 Muscular Atrophy 52 0.618
489
P NRB001 Neuroblastoma 66 0.618
490
CRV002 Cervix Uteri Carcinoma in Situ 47 0.618
491
PRC013 Pericarditis 53 0.618
492
CHL067 Cholecystitis 60 0.618
493
P MST009 Mastocytosis 64 0.618
494
HRT012 Heart Valve Disease 53 0.618
495
HLX001 Helix Syndrome 48 0.618
496
PNT003 Pinta Disease 30 0.618
497
LWC001 Low Compliance Bladder 45 0.618
498
SNS003 Sensory Peripheral Neuropathy 52 0.618
499
c ATM011 Autoimmune Hepatitis 63 0.618
500
P GLY013 Glycogen Storage Disease 60 0.618
501
SPP008 Suppurative Otitis Media 42 0.618
502
IRN001 Iron Deficiency Anemia 58 0.618
503
CHL123 Chlamydia 58 0.618
504
HMP001 Hemopericardium 47 0.618
505
TRC008 Trachoma 53 0.618
506
P PRC012 Pericardial Effusion 50 0.618
507
P INT068 Intestinal Disease 53 0.618
508
PLM029 Palmoplantar Keratosis 48 0.618
509
BRS051 Breast Disease 58 0.618
510
P GLM007 Glomerulonephritis 60 0.618
511
P EHL001 Ehlers-Danlos Syndrome 58 0.618
512
LYM021 Lymphadenitis 56 0.618
513
CHR073 Choreatic Disease 54 0.618
514
P JVN042 Juvenile Retinoschisis 39 0.618
515
P CHR345 Chronic Pain 50 0.618
516
CRV045 Cervical Intraepithelial Neoplasia 39 0.618
517
MYC021 Mycobacterium Xenopi 19 0.618
518
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 0.523
519
P RST001 Restless Legs Syndrome 52 0.523
520
c CHR521 Charcot-Marie-Tooth Disease, Type 4b1 47 0.523
521
P EPL164 Epilepsy 68 0.523
522
TBS001 Tabes Dorsalis 31 0.523
523
TYP007 Typhoid Fever 64 0.523
524
c JVN010 Juvenile Rheumatoid Arthritis 66 0.523
525
CRB087 Cerebral Arteriosclerosis 17 0.523
526
c HRD088 Hereditary Neuropathies 33 0.523
527
P PLY180 Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1 56 0.437
528
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.437
529
ZNC005 Zinc-Responsive Necrolytic Acral Erythema 15 0.437
530
PDT041 Pediatric Arterial Ischemic Stroke 17 0.437
531
P HRD217 Hereditary Optic Neuropathy 36 0.437
532
CLS049 Classic Phenylketonuria 41 0.437
533
P ALP061 Alopecia, Androgenetic, 1 49 0.437
534
c GLL024 Gallbladder Disease 1 52 0.437
535
CRD132 Cardiac Conduction Defect 60 0.437
536
TNG002 Tangier Disease 64 0.437
537
ENH001 Enhanced S-Cone Syndrome 58 0.437
538
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.437
539
ALL003 Allergic Rhinitis 67 0.437
540
CYC008 Cyclic Vomiting Syndrome 46 0.437
541
P AST005 Asthma 76 0.437
542
XNT003 Xanthomatosis 49 0.437
543
c PRG042 Progressive Familial Heart Block, Type Ia 66 0.437
544
BRK010 Burkitt Lymphoma 66 0.437
545
ACT164 Actinic Prurigo 43 0.437
546
CHN065 Choanal Atresia, Posterior 48 0.437
548
ATS010 Autosomal Recessive Disease 42 0.437
549
DFF005 Diffuse Large B-Cell Lymphoma 54 0.437
550
BRR014 Barrett Esophagus 66 0.437
551
KSH004 Kashin-Beck Disease 38 0.437
552
ASP036 Aspirin Allergy 27 0.437
553
ACT098 Acute Erythroid Leukemia 55 0.437
554
ORL019 Oral Hairy Leukoplakia 39 0.437
555
ANG061 Angular Cheilitis 28 0.437
556
THR024 Thrombosis 56 0.437
557
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.437
558
HPT046 Hepatic Veno-Occlusive Disease 62 0.437
559
CRH005 Crohn's Colitis 53 0.437
560
P FTL001 Fetal Alcohol Syndrome 55 0.437
561
AND014 Androgenic Alopecia 47 0.437
562
CLR108 Colorectal Adenoma 64 0.437
563
c GRV008 Graves Disease 1 54 0.437
564
LGH007 Leigh Syndrome 70 0.437
565
P PRP003 Porphyria Cutanea Tarda 66 0.437
566
P PLV020 Pelvic Organ Prolapse 58 0.437
567
c SCH085 Schizophrenia 2 27 0.437
568
LPT014 Leptin Deficiency or Dysfunction 78 0.437
569
c NPH068 Nephronophthisis 16 43 0.437
570
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.437
571
c HPT073 Hepatitis C Virus 71 0.437
572
ACT119 Acute Promyelocytic Leukemia 62 0.437
573
PRP083 Porphyria, Acute Intermittent 65 0.437
574
SBL008 Sea-Blue Histiocyte Disease 42 0.437
575
P MPL001 Maple Syrup Urine Disease 70 0.437
576
GLY014 Glycerol Kinase Deficiency 48 0.437
577
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.437
578
c LNG109 Lung Cancer Susceptibility 1 26 0.437
579
BTT016 Batten-Turner Congenital Myopathy 53 0.437
580
OCL069 Ocular Motor Apraxia 57 0.437
581
SPR004 Supravalvular Aortic Stenosis 57 0.437
582
P TTR001 Tetralogy of Fallot 69 0.437
583
P STR020 Strabismus 56 0.437
584
HYP732 Hyperalphalipoproteinemia 1 52 0.437
585
LCH016 Lichen Sclerosus Et Atrophicus 42 0.437
586
ANK020 Ankyloglossia with or Without Tooth Anomalies 46 0.437
587
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.437
588
OST017 Osteomyelitis 63 0.437
589
P STS003 Sitosterolemia 53 0.437
590
P MYP006 Myopia 56 0.437
591
CHR463 Chronic Actinic Dermatitis 36 0.437
592
SCT002 Scotoma 42 0.437
593
c ACT075 Acute Myocardial Infarction 56 0.437
594
MLT001 Multiple Chemical Sensitivity 39 0.437
595
P HMC002 Homocystinuria 53 0.437
596
PRP007 Priapism 47 0.437
597
CLF001 Cleft Lip 53 0.437
598
MCH006 Mechanical Strabismus 40 0.437
599
KRT006 Keratoconjunctivitis 53 0.437
600
P VSC011 Vasculitis 61 0.437
601
CHR066 Chronic Fatigue Syndrome 60 0.437
602
GLL048 Glial Tumor 52 0.437
603
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.437
604
ACT162 Acute Sensory Ataxic Neuropathy 24 0.437
605
NM001 Noma 38 0.437
606
P HYP098 Hypereosinophilic Syndrome 66 0.437
607
CLF056 Cleft Lip with or Without Cleft Palate 42 0.437
608
P RRH023 Rare Hereditary Hemochromatosis 54 0.437
609
HST010 Histiocytosis 49 0.437
610
CLL003 Cellulitis 53 0.437
611
SYS004 Systemic Mastocytosis 63 0.437
612
P CND004 Candidiasis 58 0.437
613
P GST044 Gastritis 55 0.437
614
P SYP003 Syphilis 59 0.437
615
GST040 Gastric Adenocarcinoma 67 0.437
616
ADN018 Adenoma 59 0.437
617
PRP016 Paraplegia 52 0.437
618
c LCL006 Localized Scleroderma 65 0.437
619
EBL001 Ebola Hemorrhagic Fever 56 0.437
620
BRN009 Burning Mouth Syndrome 51 0.437
621
CMB007 Combined Immunodeficiency 57 0.437
622
CMM005 Common Cold 56 0.437
623
P MGR003 Migraine with Aura 52 0.437
624
DRY001 Dry Eye Syndrome 50 0.437
625
LFT001 Left Bundle Branch Hemiblock 47 0.437
626
OST011 Osteomalacia 52 0.437
627
P MGR001 Migraine Without Aura 49 0.437
628
HMS001 Hemosiderosis 48 0.437
629
CHG001 Chagas Disease 66 0.437
630
ALL029 Allergic Disease 59 0.437
631
MRS001 Marasmus 42 0.437
632
P ESP024 Esophagitis 60 0.437
633
NTR002 Nutritional Optic Neuropathy 20 0.437
634
CRT013 Carotid Stenosis 51 0.437
635
SPN020 Spondylosis 46 0.437
636
P CLR019 Color Blindness 48 0.437
637
CHL056 Cheilitis 46 0.437
638
P NPH005 Nephronophthisis 56 0.437
639
GGR001 Geographic Tongue 39 0.437
640
P NPH012 Nephrotic Syndrome 60 0.437
641
c HRD010 Hereditary Spastic Paraplegia 66 0.437
642
CHL014 Cholera 62 0.437
643
CCC002 Coccidiosis 50 0.437
644
P ADN016 Adenocarcinoma 63 0.437
645
ACT078 Acute Porphyria 49 0.437
646
HRY002 Hairy Tongue 28 0.437
647
MDN001 Median Rhomboid Glossitis 25 0.437
648
TRN018 Transitional Cell Carcinoma 56 0.437
649
GST033 Gestational Diabetes 61 0.437
650
P BND020 Bone Disease 59 0.437
651
P MYG005 Myoglobinuria 40 0.437
652
HMP005 Hemiplegia 54 0.437
653
ORN001 Ornithosis 39 0.437
654
MCR018 Microcytic Anemia 47 0.437
655
FSS001 Fissured Tongue 30 0.437
656
TRP004 Tropical Sprue 39 0.437
657
SVR004 Severe Combined Immunodeficiency 72 0.437
658
GST050 Gastrointestinal System Disease 55 0.437
659
OST016 Osteochondrosis 52 0.437
660
P CYS039 Cystic Kidney Disease 53 0.437
661
P TCD001 Tic Disorder 49 0.437
662
PLG002 Plague 58 0.437
663
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.437
664
EXC002 Exocrine Pancreatic Insufficiency 42 0.437
665
DNT001 Dental Fluorosis 43 0.437
666
GST023 Gastric Ulcer 52 0.437
667
KRT001 Keratoconjunctivitis Sicca 50 0.437
668
FML026 Familial Lipoprotein Lipase Deficiency 52 0.437
669
HDR002 Hidradenitis Suppurativa 54 0.437
670
HDR003 Hidradenitis 50 0.437
671
PRN014 Paronychia 50 0.437
672
ESN002 Eosinophilia-Myalgia Syndrome 40 0.437
673
VSC002 Vascular Dementia 60 0.437
674
P BRN022 Bronchiectasis 60 0.437
675
XLN247 X-Linked Congenital Retinoschisis 20 0.437
676
P ACT105 Acute Mountain Sickness 52 0.437
677
GLS013 Glossodynia 16 0.437
678
GLC036 Glucagonoma 46 0.437
679
CRT011 Carotenemia 23 0.437
680
P ENC004 Encephalitis 61 0.437
681
IRR002 Irritable Bowel Syndrome 65 0.437
682
LTH004 Lathyrism 15 0.437
683
SPL018 Splenomegaly 49 0.437
684
CHL098 Childhood Myocerebrohepatopathy Spectrum 21 0.437
685
P HYP265 Hypotonia 42 0.437
686
ATN005 Autonomic Dysfunction 46 0.437
687
DYS073 Dysphagia 53 0.437
688
HYP264 Hypertonia 36 0.437
689
EXF003 Exfoliative Dermatitis 22 0.437
690
P FML187 Familial Hypertension 34 0.437
691
LKP003 Leukoplakia 39 0.437
692
MCL079 Macular Telangiectasia Type 2 27 0.437
693
MRC001 Marchiafava Bignami Disease 23 0.437
694
EXN003 Exencephaly 30 0.437
695
P MYC026 Myoclonus Epilepsy 35 0.437
696
MSL001 Measles 61 0.437
697
GLM045 Glioma 63 0.437
698
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.340
699
CNN002 Cannabis Abuse 45 0.340
700
CHR682 Chronic Bilirubin Encephalopathy 37 0.340
701
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 35 0.340
702
c PNS012 Paine Syndrome 60 0.340
703
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.340
704
c DWL002 Dowling-Degos Disease 1 58 0.340
705
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.340
706
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.340
708
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.340
709
c SYS043 Systemic Lupus Erythematosus 1 38 0.340
710
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.340
711
ABC001 Abcd Syndrome 45 0.340
712
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.340
713
c OVR114 Ovarian Cancer 1 59 0.340
714
P LFR001 Li-Fraumeni Syndrome 73 0.340
715
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.340
716
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.340
717
MNR012 Meniere Disease 56 0.340
718
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.340
719
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 59 0.340
720
P ATX030 Ataxia-Telangiectasia 80 0.340
721
BWN001 Bowen-Conradi Syndrome 53 0.340
722
ARM010 Arima Syndrome 56 0.340
723
PPL049 Papillon-Lefevre Syndrome 66 0.340
724
c LKM063 Leukemia, Chronic Myeloid 71 0.340
725
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.340
726
P SLP006 Sleep Apnea 69 0.340
727
MNT001 Mantle Cell Lymphoma 67 0.340
728
LYM012 Lymphoplasmacytic Lymphoma 50 0.340
729
CVD001 Covid-19 57 0.340
730
P PRV006 Pervasive Developmental Disorder 52 0.340
731
P PLY014 Polycystic Kidney Disease 69 0.340
732
SBJ001 Subjective Cognitive Decline 30 0.340
733
P CTN015 Cutaneous T Cell Lymphoma 48 0.340
734
WLD007 Waldenstroem's Macroglobulinemia 63 0.340
735
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.340
736
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 41 0.340
737
c FNC043 Fanconi Anemia, Complementation Group E 62 0.340
738
NRL018 Neural Tube Defects, Folate-Sensitive 45 0.340
739
c LKM061 Leukemia, Acute Myeloid 83 0.340
740
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.340
741
KHL003 Kohlschutter-Tonz Syndrome 59 0.340
742
P FRD001 Friedreich Ataxia 61 0.340
743
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 0.340
744
KRT013 Keratolytic Winter Erythema 45 0.340
745
LMY014 Leiomyoma, Uterine 56 0.340
746
c PSR028 Psoriasis 7 43 0.340
747
ACR006 Aceruloplasminemia 63 0.340
748
c BSL024 Basal Cell Carcinoma 1 55 0.340
749
c DRM054 Dermatitis, Atopic, 2 46 0.340
750
ACR041 Acromelic Frontonasal Dysostosis 53 0.340
751
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.340
752
PHL006 Phelan-Mcdermid Syndrome 60 0.340
753
c PSR017 Psoriasis 2 53 0.340
754
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.340
755
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 0.340
756
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 0.340
757
c CNG413 Congenital Short Bowel Syndrome 42 0.340
758
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 0.340
759
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.340
760
GLS018 Glass Syndrome 61 0.340
761
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.340
762
P ATX024 Ataxia-Oculomotor Apraxia 3 45 0.340
763
ACD008 Acid-Labile Subunit Deficiency 52 0.340
764
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 29 0.340
765
c PRS136 Prostate Cancer, Hereditary, 6 33 0.340
766
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.340
767
c PSR018 Psoriasis 13 52 0.340
768
c PSR023 Psoriasis 1 52 0.340
769
MLN073 Melanosis, Neurocutaneous 45 0.340
770
c CHL140 Chilblain Lupus 1 58 0.340
771
LGN006 Legionnaire Disease 52 0.340
772
c LFR007 Li-Fraumeni Syndrome 2 46 0.340
773
P JBR020 Joubert Syndrome 1 74 0.340
774
P PRC031 Preeclampsia/eclampsia 1 43 0.340
775
MYL005 Myelofibrosis 71 0.340
776
VTR016 Vater/vacterl Association 49 0.340
777
P SRC025 Sarcoidosis 1 71 0.340
778
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 57 0.340
779
c INF071 Inflammatory Bowel Disease 1 65 0.340
780
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.340
781
P PRS040 Prostate Cancer 95 0.340
782
c HYP595 Hypertension, Essential 85 0.340
783
CMR002 Coumarin Resistance 59 0.340
784
ERY029 Erythermalgia, Primary 58 0.340
785
APN008 Apnea, Obstructive Sleep 67 0.340
786
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.340
787
c LPR022 Leprosy 2 34 0.340
788
BCT022 Bacterial Infectious Disease 56 0.340
789
c PRS130 Prostate Cancer, Hereditary, 8 32 0.340
790
c PSR032 Psoriasis 11 47 0.340
791
P PTT014 Pitt-Hopkins Syndrome 64 0.340
792
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.340
793
P PRG092 Pregnancy Loss, Recurrent 1 41 0.340
794
LMY002 Leiomyoma 51 0.340
795
FML063 Familial Glucocorticoid Deficiency 58 0.340
796
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.340
797
TRM010 Traumatic Brain Injury 51 0.340
798
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 0.340
799
MCR004 Macroglobulinemia 49 0.340
800
OCL006 Ocular Hypertension 53 0.340
801
PRS034 Parasitic Helminthiasis Infectious Disease 51 0.340
802
MTC004 Mitochondrial Encephalomyopathy 42 0.340
803
HDG004 Hodgkin's Granuloma 23 0.340
804
DBT006 Diabetic Macular Edema 48 0.340
805
P MYL006 Myeloid Leukemia 61 0.340
806
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 0.340
807
CLS047 Classic Progressive Supranuclear Palsy Syndrome 33 0.340
808
PRS047 Prostatitis 58 0.340
809
CNN001 Cannabis Dependence 38 0.340
810
P CHR012 Chronic Granulomatous Disease 69 0.340
811
LNG031 Lung Benign Neoplasm 51 0.340
812
GLC008 Glucose Metabolism Disease 40 0.340
813
MYF001 Myofibroma 42 0.340
814
P THY032 Thyroiditis 57 0.340
815
LNG099 Lung Disease 62 0.340
816
MYF002 Myofascial Pain Syndrome 46 0.340
817
HMT002 Hematologic Cancer 61 0.340
818
c DRR009 Diarrhea 6 45 0.340
819
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.340
820
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.340
821
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.340
822
P CTN003 Cutaneous Lupus Erythematosus 52 0.340
823
LGN002 Legionellosis 62 0.340
824
P MLN007 Male Infertility 56 0.340
825
NWB001 Newborn Respiratory Distress Syndrome 56 0.340
826
P LTR001 Lateral Sclerosis 58 0.340
827
ACT029 Acute Interstitial Pneumonia 59 0.340
828
CNT017 Central Nervous System Origin Vertigo 44 0.340
829
HNT002 Hantavirus Pulmonary Syndrome 55 0.340
830
P HPT021 Hepatitis 69 0.340
831
SKN013 Skin Benign Neoplasm 50 0.340
832
IDP011 Idiopathic Interstitial Pneumonia 59 0.340
833
ATN004 Autonomic Neuropathy 42 0.340
834
LYM040 Lymphoblastic Lymphoma 53 0.340
835
KHN001 Kuhnt-Junius Degeneration 48 0.340
836
PRD004 Prediabetes Syndrome 52 0.340
837
PLS009 Plasma Cell Neoplasm 64 0.340
838
c HPT007 Hepatitis E 51 0.340
839
THY030 Thyroid Gland Disease 50 0.340
840
PLC008 Placenta Disease 49 0.340
841
LRY017 Laryngeal Disease 45 0.340
842
P LRY044 Larynx Cancer 54 0.340
843
P KDN017 Kidney Cancer 61 0.340
844
CNT047 Contact Dermatitis 57 0.340
845
CRB009 Cerebritis 43 0.340
846
P MTR014 Motor Neuron Disease 65 0.340
847
P OBS001 Obstructive Jaundice 48 0.340
848
ACT011 Acute Contagious Conjunctivitis 42 0.340
849
DBT002 Diabetic Autonomic Neuropathy 41 0.340
850
VCT001 Vacterl Association 47 0.340
851
SPS003 Spastic Diplegia 53 0.340
852
DBT004 Diabetic Polyneuropathy 50 0.340
853
RNL011 Renal Osteodystrophy 49 0.340
855
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.340
856
ATX019 Ataxia with Vitamin E Deficiency 44 0.340
857
BCK006 Back Pain 47 0.340
858
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.340
859
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.340
860
NNN007 Non-Involuting Congenital Hemangioma 40 0.340
861
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 0.340
862
c PRM038 Primary Agammaglobulinemia 47 0.340
863
RSP007 Respiratory Distress Syndrome, Infant 40 0.340
864
CHL079 Children's Interstitial Lung Disease 26 0.340
865
c CHR064 Chronic Monocytic Leukemia 36 0.340
866
HDG006 Hodgkin's Paragranuloma 21 0.340
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