Search results for Iron

4236 hits were found for Iron

# Family MCID Name MIFTS Score
1
IRN002 Iron Metabolism Disease 57 172.310
2
P RRH023 Rare Hereditary Hemochromatosis 54 107.403
3
IRN001 Iron Deficiency Anemia 58 104.699
4
HMS001 Hemosiderosis 48 101.027
5
DFC004 Deficiency Anemia 74 96.615
6
c HMC039 Hemochromatosis, Type 1 73 68.405
7
IRN004 Iron-Refractory Iron Deficiency Anemia 46 58.901
8
P THL005 Thalassemia 56 46.872
9
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 42.468
10
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 39.674
11
IRN008 Iron Overload in Africa 51 37.325
12
c NRD032 Neurodegeneration with Brain Iron Accumulation 5 51 35.499
13
MCR018 Microcytic Anemia 47 34.364
14
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 32.014
15
c NRD014 Neurodegeneration with Brain Iron Accumulation 4 41 31.942
16
c CHR684 Chronic Kidney Disease 69 31.865
17
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 31.453
18
c NRD016 Neurodegeneration with Brain Iron Accumulation 6 50 30.917
19
c NRD008 Neurodegeneration with Brain Iron Accumulation 3 54 30.432
20
c NRD009 Neurodegeneration with Brain Iron Accumulation 2b 44 29.842
21
c BTT014 Beta-Thalassemia 72 29.588
22
P SDR002 Siderosis 43 29.549
23
GRC001 Gracile Syndrome 47 28.340
24
c HMC034 Hemochromatosis, Type 5 41 28.054
25
P KDN018 Kidney Disease 72 27.752
26
P HYP252 Hypochromic Microcytic Anemia with Iron Overload 19 26.176
27
c ANM036 Anemia, Sideroblastic, 1 56 25.411
28
c ANM027 Anemia, Hypochromic Microcytic, with Iron Overload 2 26 22.483
29
MYL009 Myelodysplastic Syndrome 67 21.804
30
MTC036 Mitochondrial Membrane Protein-Associated Neurodegeneration 25 21.640
31
P INF037 Inflammatory Bowel Disease 53 21.256
32
c HMC009 Hemochromatosis Type 2 53 21.123
33
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 20.605
34
P SDR003 Sideroblastic Anemia 51 20.272
35
P SCK005 Sickle Cell Disease 56 19.875
36
CNG034 Congestive Heart Failure 69 19.482
37
NTR005 Nutritional Deficiency Disease 61 19.341
38
P RST001 Restless Legs Syndrome 52 19.289
39
END086 End Stage Renal Disease 52 18.797
40
P LVR013 Liver Disease 69 18.774
41
NNL005 Non-Alcoholic Fatty Liver Disease 63 17.994
42
c NRD047 Neurodegeneration with Brain Iron Accumulation 7 22 17.831
43
c NRD048 Neurodegeneration with Brain Iron Accumulation 8 20 17.831
44
ACR006 Aceruloplasminemia 63 17.649
45
KRT002 Keratomalacia 55 17.183
46
BTT017 Beta-Thalassemia Major 51 17.173
47
RPD005 Rapidly Involuting Congenital Hemangioma 46 17.101
48
P CLC063 Celiac Disease 1 66 17.016
49
FTT001 Fatty Liver Disease 62 16.703
50
P PRP029 Porphyria 60 16.621
51
HYP266 Hypoxia 57 16.616
52
LVR012 Liver Cirrhosis 63 16.395
53
MLR004 Malaria 80 16.026
54
LYM125 Lymphedema, Cardiac Septal Defects, and Characteristic Facies 21 15.832
55
AGN016 Aging 54 15.749
56
P HRT032 Heart Disease 81 15.536
57
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 15.507
58
SCK003 Sickle Cell Anemia 74 15.227
59
HMG005 Hemoglobinopathy 56 15.086
60
P PRP003 Porphyria Cutanea Tarda 66 14.655
61
c HPT001 Hepatitis C 62 14.461
62
HYP001 Hypochromic Microcytic Anemia 37 14.448
63
P GST044 Gastritis 55 14.258
64
P FRD001 Friedreich Ataxia 61 13.993
65
P HML002 Hemolytic Anemia 62 13.892
66
HLC007 Helicobacter Pylori Infection 67 13.807
67
P PRK039 Parkinsonism 55 13.050
68
ATS010 Autosomal Recessive Disease 42 12.835
69
P ALZ034 Alzheimer Disease 87 12.814
70
VTM002 Vitamin B12 Deficiency 48 12.588
71
P MLT020 Multiple Sclerosis 79 12.579
72
RCK004 Rickets 68 12.483
73
CRH001 Crohn's Disease 80 12.406
74
BCT022 Bacterial Infectious Disease 56 12.115
75
CNS004 Constipation 56 12.010
76
NNL006 Non-Alcoholic Steatohepatitis 54 11.981
77
MYP025 Myopathy with Deficiency of Iron-Sulfur Cluster Assembly Enzyme 11 11.976
78
P NRB001 Neuroblastoma 66 11.944
79
P PLM037 Pulmonary Hypertension 72 11.820
80
HLX001 Helix Syndrome 48 11.799
81
ULC004 Ulcerative Colitis 74 11.675
82
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 11.645
83
MYP097 Myopathy with Lactic Acidosis, Hereditary 31 11.444
84
P PRK057 Parkinson Disease, Late-Onset 80 11.436
85
HYP080 Hypogonadism 50 11.423
86
c ATR087 Atrial Standstill 1 74 11.390
87
P ART023 Arthropathy 61 11.381
88
ATH013 Atherosclerosis Susceptibility 63 11.381
89
c AMY091 Amyotrophic Lateral Sclerosis 1 88 11.374
90
c HPT073 Hepatitis C Virus 71 11.322
91
P DRR001 Diarrhea 55 11.287
92
P LTR001 Lateral Sclerosis 58 11.273
93
THR004 Thrombocytosis 53 11.255
94
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 11.099
95
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 11.099
96
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 11.099
97
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 11.099
98
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 11.099
99
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 11.099
100
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 11.099
101
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 11.099
102
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 11.099
103
HYP017 Hypophosphatemia 49 11.049
104
IRN005 Irons Bhan Syndrome 7 11.034
105
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 11.005
106
c HMC035 Hemochromatosis, Type 4 52 11.000
107
c VRL010 Viral Hepatitis 53 10.937
108
P HYP086 Hypothyroidism 69 10.861
109
P APL001 Aplastic Anemia 73 10.700
110
P DBT009 Diabetes Mellitus 67 10.610
111
GST033 Gestational Diabetes 61 10.603
113
c ALP101 Alpha-Thalassemia 62 10.567
114
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 10.518
115
MYP009 Myopathy with Deficiency of Iscu 12 10.500
116
48X005 48,xyyy 39 10.452
117
CLT003 Colitis 63 10.446
118
P PLY018 Polycythemia 56 10.348
119
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 10.303
120
P DYS154 Dystonia 64 10.299
121
P HPT021 Hepatitis 69 10.258
122
CYS001 Cystic Fibrosis 78 10.247
123
GNT037 Genetic Hyperferritinemia Without Iron Overload 11 10.170
124
PRT251 Proteinuria, Chronic Benign 57 10.069
126
P MYC084 Mycobacterium Tuberculosis 1 68 9.950
127
HYP801 Hyperferritinemia with or Without Cataract 53 9.943
128
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 9.916
129
P HNT016 Huntington Disease 73 9.878
130
P ALC033 Alcohol Use Disorder 61 9.734
131
P CLR023 Colorectal Cancer 100 9.731
132
PCD001 Pica Disease 38 9.705
133
HMP009 Haemophilus Influenzae 41 9.701
134
c TYP009 Type 2 Diabetes Mellitus 92 9.659
135
KRK002 Karak Syndrome 17 9.614
136
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 9.591
137
DSS032 Disease by Infectious Agent 55 9.522
138
SPL018 Splenomegaly 49 9.485
139
P HPT023 Hepatocellular Carcinoma 96 9.409
140
HMC038 Hemochromatosis, Neonatal 33 9.398
141
c PRC016 Pre-Eclampsia 65 9.355
142
RFR010 Refractory Anemia 49 9.354
143
P BRS047 Breast Cancer 98 9.212
144
P RTN016 Retinal Degeneration 52 9.162
145
P MVM001 Movement Disease 61 9.133
146
ALL029 Allergic Disease 59 9.119
147
CNS020 Constitutional Anemia Due to Iron Metabolism Disorder 4 9.047
148
ACT098 Acute Erythroid Leukemia 55 8.953
149
P NTR004 Neutropenia 63 8.949
150
HYP025 Hyperphosphatemia 48 8.924
151
47X002 47,xyy 48 8.922
152
GRN017 Granulocytopenia 42 8.891
153
DSR030 Disorder of Iron Metabolism and Transport 3 8.750
154
P CRN300 Coronary Heart Disease 1 73 8.680
155
c LKM061 Leukemia, Acute Myeloid 83 8.585
156
P THR014 Thrombocytopenia 66 8.584
157
P ZLL001 Zellweger Syndrome 65 8.570
158
HYP781 Hypoascorbemia 52 8.528
159
PLM049 Plummer Vinson Syndrome 32 8.519
160
ALC007 Alcohol Dependence 66 8.487
161
URM002 Uremia 47 8.485
162
PRT036 Peritonitis 65 8.480
163
P ATT013 Attention Deficit-Hyperactivity Disorder 64 8.460
164
LNG099 Lung Disease 62 8.454
165
GLL048 Glial Tumor 52 8.424
166
P KLZ004 Kala-Azar 1 41 8.390
167
LSH001 Leishmaniasis 64 8.390
168
MYL005 Myelofibrosis 71 8.348
169
GLB002 Glioblastoma 67 8.320
170
GLM045 Glioma 63 8.308
171
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 8.306
172
CYT002 Cytokine Deficiency 43 8.299
173
BRN071 Brain Injury 50 8.212
174
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 8.061
175
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 8.061
176
P OST002 Osteoporosis 76 8.054
177
c ACT073 Acute Leukemia 58 8.048
178
ISC004 Ischemia 61 8.036
179
c HMC010 Hemochromatosis, Type 3 49 8.035
180
P LKM002 Leukemia 67 8.027
181
FRR002 Ferro-Cerebro-Cutaneous Syndrome 10 8.016
182
P VSC007 Vascular Disease 63 8.012
183
c DNT047 Dentinogenesis Imperfecta Type 2 35 8.010
184
P TRM003 Tremor 48 7.966
185
PLM129 Pulmonary Disease, Chronic Obstructive 74 7.883
186
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 7.852
187
P END044 Endometriosis 62 7.845
188
P CTR002 Cataract 60 7.840
189
TLN003 Telangiectasis 51 7.838
190
DPH001 Diphtheria 59 7.818
191
BNR002 Bone Resorption Disease 47 7.814
192
P MYC007 Myocardial Infarction 70 7.729
193
P ATR005 Atrophic Gastritis 50 7.705
194
ATR002 Atransferrinemia 50 7.646
195
CHL123 Chlamydia 58 7.646
196
MGL001 Megaloblastic Anemia 58 7.622
197
c ACT071 Acute Kidney Failure 60 7.592
198
c PRT132 Protoporphyria, Erythropoietic, 1 61 7.590
199
c PLM164 Pulmonary Hypertension, Primary, 1 76 7.589
200
P EXN002 Exanthem 58 7.543
201
PST092 Posttransplant Acute Limbic Encephalitis 28 7.535
202
P ADN016 Adenocarcinoma 63 7.509
203
THL010 Thalassemia Minor 32 7.406
204
P HYP069 Hyperparathyroidism 62 7.323
205
DYS073 Dysphagia 53 7.307
206
HYP066 Hyperglycemia 61 7.281
207
MYL069 Myeloma, Multiple 77 7.270
208
SLC011 Silicosiderosis 8 7.247
209
ARN001 Arena Syndrome 5 7.247
210
P PLM085 Pulmonary Hemosiderosis 44 7.210
211
ACT058 Active Peptic Ulcer Disease 56 7.200
212
OST011 Osteomalacia 52 7.176
213
HRW001 Hair Whorl 35 7.168
214
P CNG003 Congenital Dyserythropoietic Anemia 48 7.167
215
P INT068 Intestinal Disease 53 7.165
216
c ACT068 Acute Cystitis 61 7.159
217
PPT005 Peptic Ulcer Disease 58 7.148
218
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 7.118
219
PRT037 Pertussis 65 7.078
220
PRN011 Pernicious Anemia 53 7.076
221
SPN186 Spinal Cord Injury 61 7.074
222
P URN019 Urinary Tract Infection 49 7.071
223
WLS001 Wilson Disease 70 7.050
224
P BND020 Bone Disease 59 7.034
225
MTH071 Methane Production 25 6.999
226
c MCR120 Microvascular Complications of Diabetes 7 47 6.974
227
MCR141 Mucormycosis 59 6.940
228
ADN018 Adenoma 59 6.936
229
P GST053 Gastric Cancer 83 6.932
230
PLY001 Polycythemia Vera 69 6.866
231
P PRD008 Periodontitis 64 6.861
232
ART140 Arteries, Anomalies of 53 6.827
233
DWN001 Down Syndrome 70 6.819
234
STR067 Stroke, Ischemic 80 6.810
235
LPP008 Lipoprotein Quantitative Trait Locus 65 6.799
236
P LKM062 Leukemia, Acute Lymphoblastic 69 6.798
237
RLP002 Relapsing-Remitting Multiple Sclerosis 56 6.793
238
GLC003 Glucose Intolerance 54 6.791
239
PRT038 Protein-Energy Malnutrition 53 6.785
240
ANX004 Anoxia 40 6.769
241
P SLP005 Sleep Disorder 61 6.725
242
P PNC035 Pancreatic Cancer 86 6.689
243
P ATS364 Autism 69 6.680
244
PLS007 Plasmodium Falciparum Malaria 52 6.668
245
P MYP004 Myopathy 67 6.667
246
P PNM007 Pneumonia 67 6.666
247
P RTN018 Retinal Disease 53 6.654
248
ALL014 Allergic Encephalomyelitis 34 6.639
249
P MYL006 Myeloid Leukemia 61 6.636
250
c HYP836 Hypercholesterolemia, Familial, 1 73 6.628
251
P SZR006 Seizure Disorder 70 6.625
252
MLT157 Multiple System Atrophy 1 69 6.622
253
P INF032 Infertility 57 6.603
254
GTR002 Goiter 53 6.586
255
P RHM011 Rheumatoid Arthritis 82 6.464
256
c HPT016 Hepatitis B 62 6.464
257
P ECL001 Eclampsia 52 6.447
258
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 6.430
259
SCH014 Schistosomiasis 56 6.430
260
MLD018 Mild Cognitive Impairment 48 6.415
261
ANT018 Anthracosis 51 6.413
262
SYS003 Systolic Heart Failure 49 6.405
263
DNT012 Dental Caries 53 6.382
264
P PRS040 Prostate Cancer 95 6.371
265
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 6.361
266
BRN004 Brain Edema 54 6.307
267
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 6.302
268
c MCR130 Microvascular Complications of Diabetes 6 41 6.254
269
MCR017 Macrocytic Anemia 44 6.241
270
GST050 Gastrointestinal System Disease 55 6.237
271
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 6.222
272
HMG002 Hemoglobinuria 50 6.220
273
P DMN002 Dementia 66 6.220
274
c MCR113 Microvascular Complications of Diabetes 3 52 6.215
275
c MCR133 Microvascular Complications of Diabetes 4 41 6.215
276
ANG011 Angiodysplasia 42 6.184
277
LPT014 Leptin Deficiency or Dysfunction 78 6.176
278
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 6.171
279
P ART022 Arthritis 71 6.167
280
ENT011 Enterocolitis 55 6.156
281
PLG002 Plague 58 6.148
282
c HYP595 Hypertension, Essential 85 6.135
283
RNL114 Renal Cell Carcinoma, Nonpapillary 80 6.124
284
P LNG032 Lung Cancer 98 6.124
285
P LYM118 Lymphoma 67 6.118
286
NRL016 Neural Tube Defects 81 6.118
287
ATM095 Autoimmune Disease 61 6.112
288
P PNM006 Pneumoconiosis 55 6.111
289
PRP027 Peripheral Vascular Disease 71 6.096
290
P ENC018 Encephalopathy 62 6.076
291
c ATS007 Autism Spectrum Disorder 72 6.055
292
HYP060 Hyperinsulinism 54 6.039
293
P OVR042 Ovarian Cancer 88 6.039
294
BTT018 Beta-Thalassemia Intermedia 31 6.033
295
CRH005 Crohn's Colitis 53 6.032
296
THR024 Thrombosis 56 5.980
297
c HMG003 Hemoglobin E Disease 42 5.969
298
P BNG032 Benign Mesothelioma 53 5.969
299
GST045 Gastroenteritis 58 5.946
300
P ADL010 Adult Respiratory Distress Syndrome 71 5.944
301
P RCT021 Rectum Cancer 54 5.938
302
P ALP008 Alopecia 54 5.932
303
PLM001 Pulmonary Tuberculosis 69 5.927
304
OST159 Osteogenic Sarcoma 66 5.909
305
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 53 5.909
306
ANC001 Ancylostomiasis 39 5.895
307
CHL068 Cholestasis 61 5.867
308
ANM001 Anemia of Prematurity 31 5.862
309
P CND004 Candidiasis 58 5.861
310
P NRP001 Neuropathy 60 5.857
311
c DLT002 Dilated Cardiomyopathy 78 5.843
312
OST012 Osteoarthritis 77 5.841
313
P ESP024 Esophagitis 60 5.827
314
BRT055 Breath-Holding Spells 28 5.810
315
CHL014 Cholera 62 5.809
316
LPD008 Lipid Metabolism Disorder 62 5.808
317
P GRF003 Graft-Versus-Host Disease 71 5.808
318
PLC008 Placenta Disease 49 5.807
319
c ACT075 Acute Myocardial Infarction 56 5.806
320
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 52 5.799
322
c EXD008 Exudative Vitreoretinopathy 1 71 5.764
323
ESP021 Esophageal Cancer 83 5.763
324
P PLM036 Pulmonary Fibrosis 66 5.754
325
CRB039 Cerebrovascular Disease 66 5.751
326
GST020 Gastric Antral Vascular Ectasia 40 5.745
327
VSC003 Visceral Leishmaniasis 55 5.739
328
c MGR028 Migraine with or Without Aura 1 64 5.730
329
PST021 Postpartum Depression 50 5.719
330
BLR008 Bilirubin Metabolic Disorder 57 5.691
331
ACQ007 Acquired Immunodeficiency Syndrome 59 5.682
332
P SPR120 Supranuclear Palsy, Progressive, 1 69 5.666
333
P HRD011 Hereditary Spherocytosis 64 5.643
334
PNC001 Pancytopenia 53 5.642
335
GLS007 Glossitis 47 5.602
336
P NPH012 Nephrotic Syndrome 60 5.577
337
c HPT003 Hepatitis a 63 5.568
338
SYN007 Synovitis 55 5.550
339
IMM167 Immune Deficiency Disease 78 5.502
340
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 35 5.475
341
c RST012 Restless Legs Syndrome 1 33 5.457
342
P AMY004 Amyloidosis 70 5.452
343
P GLM007 Glomerulonephritis 60 5.452
344
c SPS153 Spastic Paraplegia 35, Autosomal Recessive 50 5.452
345
P HYP098 Hypereosinophilic Syndrome 66 5.410
346
c TYP008 Type 1 Diabetes Mellitus 70 5.404
347
CND006 Candida Glabrata 30 5.403
348
OTT002 Otitis Media 71 5.400
349
TRM010 Traumatic Brain Injury 51 5.389
350
AMN001 Amenorrhea 54 5.387
351
PRT013 Portal Hypertension 59 5.383
352
TXC005 Toxic Shock Syndrome 62 5.381
353
P PRP019 Peripheral Nervous System Disease 58 5.353
354
P PNC044 Pancreatitis 61 5.352
355
P DMN001 Diamond-Blackfan Anemia 71 5.349
356
c ATM101 Autoimmune Gastritis 40 5.321
357
P HMN010 Hemangioma 62 5.306
358
HMN044 Human Immunodeficiency Virus Type 1 78 5.300
359
P URT039 Urticaria 58 5.299
360
P ASP006 Aspergillosis 72 5.279
361
c HMC021 Hemochromatosis, Type 2a 41 5.266
362
PRP030 Purpura 54 5.254
363
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 5.242
364
P FBR031 Febrile Seizures 52 5.235
365
DPR016 Depression 65 5.230
366
P HYP730 Hypogonadotropic Hypogonadism 53 5.226
367
P PLY011 Polycystic Ovary Syndrome 57 5.226
368
P BCL017 B-Cell Lymphoma 59 5.223
369
PLC002 Plica Syndrome 35 5.217
370
P SLP006 Sleep Apnea 69 5.210
371
TTN003 Tetanus 65 5.202
372
P BRS044 Breast Adenocarcinoma 58 5.183
373
P DDN001 Duodenal Ulcer 53 5.182
374
BRN024 Bronchitis 67 5.170
375
KFR001 Kufor-Rakeb Syndrome 59 5.169
376
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 5.158
377
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 5.142
378
CRB004 Cerebral Artery Occlusion 45 5.134
379
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 5.122
380
LMY002 Leiomyoma 51 5.122
381
P OVR082 Overgrowth Syndrome 49 5.115
382
DYS015 Dysentery 50 5.112
383
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 5.092
384
c DWL002 Dowling-Degos Disease 1 58 5.090
385
ETN001 Eating Disorder 59 5.059
386
P SRC025 Sarcoidosis 1 71 5.028
387
STM007 Stomatitis 54 5.003
388
P TRN020 Turner Syndrome 67 5.003
389
PPL052 Papillomatosis, Confluent and Reticulated 34 4.993
390
P HYP024 Hypoparathyroidism 55 4.982
391
P ART005 Arteriovenous Malformation 65 4.963
392
c SCN007 Secondary Hyperparathyroidism 51 4.957
393
P LCT001 Lactic Acidosis 51 4.897
394
HMC014 Homocysteinemia 52 4.892
395
P HMG032 Hemoglobin H Disease 51 4.882
396
c MCR115 Microvascular Complications of Diabetes 5 65 4.871
397
SPN035 Spindle Cell Sarcoma 54 4.865
398
SRC014 Sarcoma 65 4.865
399
PRN019 Perinatal Necrotizing Enterocolitis 60 4.863
400
P VSC011 Vasculitis 61 4.857
401
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 52 4.853
402
MNT002 Mental Depression 57 4.853
403
GRD001 Giardiasis 46 4.850
404
ORL011 Oral Cancer 60 4.846
405
SCR011 Scrapie 39 4.844
406
P MLN008 Melanoma 76 4.833
407
P PRN023 Prion Disease 60 4.817
408
GST092 Gastroesophageal Reflux 61 4.804
409
ANR040 Aneurysm 61 4.802
410
P SNS001 Sensorineural Hearing Loss 59 4.797
411
NRD068 Neurodegeneration, Early-Onset, with Choreoathetoid Movements and Microcytic Anemia 22 4.796
412
c GLL024 Gallbladder Disease 1 52 4.793
413
GST023 Gastric Ulcer 52 4.789
414
RBF001 Riboflavin Deficiency 49 4.781
415
P THY032 Thyroiditis 57 4.758
416
P HYP076 Hyperthyroidism 53 4.752
417
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 4.735
418
PTT016 Patterson Pseudoleprechaunism Syndrome 28 4.734
419
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 25 4.719
420
LYM133 Lymphoma, Hodgkin, Classic 74 4.713
421
P RSP003 Respiratory Failure 74 4.710
422
P EPL164 Epilepsy 68 4.685
423
IMP005 Impotence 52 4.683
424
P LPS004 Lupus Erythematosus 61 4.676
425
P CRD246 Cardiovascular System Disease 56 4.656
426
ATR073 Atrophic Glossitis 31 4.647
427
MYM001 Myoma 54 4.640
428
CVD001 Covid-19 57 4.633
429
RDC006 Red Cell Aplasia 44 4.632
430
VRC005 Varicose Veins 60 4.629
431
NRX001 Neuroaxonal Dystrophy 38 4.623
432
ORL004 Oral Submucous Fibrosis 56 4.592
433
SPR066 Superficial Siderosis 38 4.586
434
PHN003 Phenylketonuria 76 4.575
435
P LPR021 Leprosy 3 71 4.533
436
HNS001 Hansen's Disease 32 4.533
437
P GLM040 Glioma Susceptibility 1 71 4.532
438
DMY004 Demyelinating Disease 50 4.526
439
c SYS001 Systemic Lupus Erythematosus 87 4.524
440
P BLD134 Bladder Cancer 79 4.524
441
P PHC003 Pheochromocytoma 69 4.520
442
c PCH010 Pachyonychia Congenita 3 43 4.512
443
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 47 4.506
444
CRY005 Cryptococcosis 60 4.500
445
HRN026 Hernia, Hiatus 47 4.497
446
c ACT027 Acute Pancreatitis 60 4.496
447
P HYP750 Hypertriglyceridemia, Familial 62 4.488
448
HYP056 Hypoglycemia 65 4.488
449
c ACT134 Acute Liver Failure 59 4.485
450
P MYC008 Myocarditis 59 4.476
451
SVR004 Severe Combined Immunodeficiency 72 4.474
452
P PYL005 Pyelonephritis 57 4.466
453
PRS034 Parasitic Helminthiasis Infectious Disease 51 4.447
454
c BRN108 Branchiootic Syndrome 1 62 4.446
455
SLC006 Silicosis 56 4.446
456
MST005 Mastitis 53 4.440
457
TYP007 Typhoid Fever 64 4.439
458
PRD002 Periodic Limb Movement Disorder 34 4.432
460
ART016 Aortic Aneurysm 68 4.409
461
P ANP001 Anaplastic Large Cell Lymphoma 61 4.404
462
ANX010 Anxiety 70 4.391
463
c LKM063 Leukemia, Chronic Myeloid 71 4.382
464
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.369
465
PST011 Pustulosis of Palm and Sole 52 4.363
466
c ATM011 Autoimmune Hepatitis 63 4.355
467
MTB004 Metabolic Acidosis 48 4.354
468
SVR001 Severe Acute Respiratory Syndrome 67 4.354
469
SKN016 Skin Disease 63 4.353
470
P PSR002 Psoriasis 63 4.347
471
LYM027 Lymphopenia 56 4.347
472
DRM006 Dermatitis 62 4.339
473
INS024 Insulin-Like Growth Factor I 78 4.327
474
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 4.322
475
CHR073 Choreatic Disease 54 4.322
476
PLM031 Poliomyelitis 63 4.319
477
ADL002 Adult Syndrome 70 4.318
478
P THR015 Thrombophilia 51 4.318
479
P ESS003 Essential Thrombocythemia 69 4.288
480
P MCR129 Microvascular Complications of Diabetes 1 68 4.286
481
ALC009 Alcoholic Liver Cirrhosis 54 4.283
482
ALC006 Alcoholic Hepatitis 61 4.280
483
P PRR002 Pure Red-Cell Aplasia 47 4.272
484
BLR027 Blue Rubber Bleb Nevus 40 4.265
485
P HYD006 Hydrocephalus 61 4.250
486
LYM143 Lymphoma, Non-Hodgkin, Familial 75 4.249
487
RHB024 Rhabdomyosarcoma 2 67 4.248
488
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 4.244
489
BRN028 Brain Cancer 74 4.242
490
CLR108 Colorectal Adenoma 64 4.233
491
ANT024 Anthrax Disease 58 4.233
492
KWS001 Kwashiorkor 45 4.232
493
P GCH001 Gaucher's Disease 70 4.215
494
P FBR017 Fibrosarcoma 56 4.215
495
P CRD119 Cardiac Arrest 67 4.211
496
P RHN004 Rhinitis 57 4.198
497
MLG169 Malignant Astrocytoma 57 4.187
498
c PLM127 Pulmonary Hypertension, Primary, 3 34 4.186
499
P SLM003 Salmonellosis 54 4.183
500
P LKM071 Leukemia, Chronic Lymphocytic 75 4.181
501
c PRP091 Porphyria Cutanea Tarda, Type I 30 4.177
502
P MSC005 Muscular Dystrophy 67 4.171
503
GST040 Gastric Adenocarcinoma 67 4.153
504
NSS002 Neisseria Meningitidis Infection 47 4.143
505
SPS057 Spasticity 42 4.142
506
P INF038 Influenza 68 4.134
507
CHL065 Cholangiocarcinoma 58 4.123
508
INT079 Intrahepatic Cholangiocarcinoma 51 4.123
509
P END033 Endocarditis 58 4.114
510
P LNG064 Lung Cancer Susceptibility 3 70 4.089
511
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 4.088
512
CHR105 Choreoacanthocytosis 55 4.079
513
CLN015 Colon Adenocarcinoma 65 4.078
514
ATM060 Autoimmune Atrophic Gastritis 19 4.052
515
MYL031 Myeloproliferative Neoplasm 66 4.028
516
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 4.026
517
MSL001 Measles 61 4.015
518
P KDN017 Kidney Cancer 61 4.010
519
FBR047 Fibromyalgia 58 4.007
520
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 4.004
521
c ANM038 Anemia, Autoimmune Hemolytic 64 3.998
522
c FNC027 Fanconi Anemia, Complementation Group a 81 3.945
523
P AST005 Asthma 76 3.936
524
APH001 Aphthous Stomatitis 58 3.936
525
c FML324 Familial Porphyria Cutanea Tarda 29 3.935
526
DDN006 Duodenitis 50 3.934
527
ESN011 Eisenmenger Syndrome 47 3.923
528
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.922
529
P ATR011 Atrial Fibrillation 66 3.918
530
CYN002 Cyanosis, Transient Neonatal 43 3.913
531
DWR001 Dwarfism 44 3.909
532
P HRP006 Herpes Simplex 65 3.902
533
SQM006 Squamous Cell Carcinoma 60 3.901
534
P NGH001 Night Blindness 52 3.897
535
PRP082 Porphyria, Congenital Erythropoietic 56 3.880
536
NPH018 Nephrogenic Systemic Fibrosis 49 3.878
537
ADR040 Adrenal Gland Pheochromocytoma 46 3.863
538
KPS004 Kaposi Sarcoma 77 3.861
539
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 3.851
540
CHR074 Choriocarcinoma 46 3.839
541
NRR001 Neuroretinitis 42 3.828
542
RTN023 Retinitis 46 3.828
543
CHG001 Chagas Disease 66 3.813
544
END028 Endemic Goiter 41 3.798
545
LYM019 Lymphosarcoma 46 3.793
546
ASB001 Asbestosis 47 3.793
547
ASB003 Asbestos Intoxication 32 3.793
548
OCL069 Ocular Motor Apraxia 57 3.789
549
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 3.776
550
P SYP003 Syphilis 59 3.776
551
OST017 Osteomyelitis 63 3.770
552
MNN020 Meningococcal Infection 45 3.762
553
MTC005 Mitochondrial Metabolism Disease 45 3.746
554
ANG054 Angina Pectoris 66 3.744
555
STN013 Stenotrophomonas Maltophilia Infection 26 3.732
556
MNG007 Manganese Poisoning 28 3.724
557
c MST023 Mesothelioma, Malignant 56 3.716
558
c THR092 Thrombophilia Due to Thrombin Defect 74 3.713
559
HSH003 Hashimoto Thyroiditis 60 3.701
560
P ACT105 Acute Mountain Sickness 52 3.693
561
HPT046 Hepatic Veno-Occlusive Disease 62 3.683
562
c PRD040 Periodontitis, Chronic 52 3.683
563
P HYP061 Hypertrophic Cardiomyopathy 69 3.673
564
TRD006 Tardive Dyskinesia 53 3.673
565
VRG001 Variegate Porphyria 56 3.670
566
P CHL066 Cholangitis 52 3.670
567
P HDC001 Headache 57 3.668
568
P MTH007 Methemoglobinemia 46 3.655
569
HYP063 Hypersplenism 52 3.655
570
CRV035 Cervical Cancer 73 3.650
571
BRN056 Bronchopulmonary Dysplasia 56 3.646
572
DMP001 Dumping Syndrome 43 3.645
573
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 3.633
574
c HMC019 Hemochromatosis, Type 2b 36 3.627
575
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 3.620
576
INV001 Invasive Aspergillosis 49 3.618
577
P MTR014 Motor Neuron Disease 65 3.615
578
PRP016 Paraplegia 52 3.608
579
P RTN008 Retinitis Pigmentosa 80 3.607
580
P MSC003 Muscular Atrophy 52 3.602
581
ADL030 Adult-Onset Still's Disease 59 3.601
582
c PRK071 Parkinson Disease 14, Autosomal Recessive 42 3.594
583
HMT002 Hematologic Cancer 61 3.589
584
PRM236 Primary Biliary Cholangitis 60 3.577
585
CNT047 Contact Dermatitis 57 3.574
586
GT001 Gout 64 3.573
587
BRK010 Burkitt Lymphoma 66 3.566
588
NNT011 Neonatal Anemia 34 3.562
589
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 3.559
590
PPL022 Papilloma 53 3.550
591
LST001 Listeriosis 59 3.550
592
INS001 Insulinoma 59 3.533
593
SYN036 Syncope 45 3.533
594
P VNS003 Venous Insufficiency 55 3.529
595
SQM002 Squamous Cell Papilloma 46 3.508
596
c ART101 Aortic Valve Disease 2 66 3.507
597
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 3.506
598
BRC012 Brucellosis 66 3.505
599
CRB037 Cerebral Palsy 67 3.504
600
MNN009 Meningoencephalitis 48 3.503
601
CHR100 Chronic Ulcer of Skin 57 3.494
602
VSC002 Vascular Dementia 60 3.493
603
MYF001 Myofibroma 42 3.487
604
CHL147 Chlamydia Pneumonia 47 3.484
605
P HMR005 Hemorrhoid 49 3.476
606
P MTC069 Mitochondrial Disorders 57 3.474
607
TRC003 Trichomoniasis 53 3.474
608
THR100 Thrombocytopenic Purpura, Autoimmune 61 3.464
609
P HMP007 Hemophilia 52 3.464
610
P CHR345 Chronic Pain 50 3.462
611
TRN015 Transient Cerebral Ischemia 63 3.460
612
INT323 Intraocular Pressure Quantitative Trait Locus 64 3.458
613
PLM134 Pulmonary Fibrosis, Idiopathic 76 3.457
614
c CHR417 Chronic Graft Versus Host Disease 55 3.450
615
P NRN021 Neuronal Ceroid Lipofuscinosis 65 3.450
616
c ANM042 Anemia, Congenital Dyserythropoietic, Type Ii 50 3.445
617
CTN007 Cutaneous Leishmaniasis 62 3.444
618
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 3.444
619
ANT039 Antisynthetase Syndrome 55 3.433
620
CRT072 Creutzfeldt-Jakob Disease 68 3.424
621
BRR014 Barrett Esophagus 66 3.419
622
STT009 Sutton Disease 2 29 3.417
623
P SPP010 Suppressor of Tumorigenicity 3 51 3.407
624
HYP068 Hyperostosis 47 3.383
625
GNG013 Gingivitis 59 3.383
626
P RBL001 Rubella 58 3.382
627
P LKD001 Leukodystrophy 59 3.380
628
DRG024 Drug Allergy 40 3.370
629
HVY002 Heavy Metal Poisoning 22 3.369
630
HPT022 Hepatoblastoma 54 3.352
631
INT017 Intestinal Schistosomiasis 51 3.349
632
MNN043 Meningioma, Familial 79 3.337
633
SPN021 Spinal Meningioma 50 3.337
634
ATX019 Ataxia with Vitamin E Deficiency 44 3.335
635
PSY004 Psychotic Disorder 66 3.332
636
P KRT007 Keratoconus 50 3.329
637
P MNN013 Meningitis 65 3.329
638
CHL004 Cholelithiasis 49 3.318
639
HYP005 Hypokalemia 55 3.312
640
P SCH015 Schizophrenia 74 3.309
641
c INH020 Inherited Metabolic Disorder 48 3.304
642
APP008 Appendicitis 62 3.301
643
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 3.297
644
ARG004 Argyria 26 3.286
645
c CNG027 Congenital Hemolytic Anemia 48 3.274
646
ILS001 Ileus 50 3.271
647
P SKN015 Skin Carcinoma 71 3.270
648
ANR007 Anorexia Nervosa 60 3.261
649
MLD001 Melioidosis 67 3.259
650
PLM033 Pulmonary Embolism 58 3.254
651
IRR002 Irritable Bowel Syndrome 65 3.253
652
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 3.245
653
P ACN011 Acne 57 3.238
654
CTN011 Cutaneous Porphyria 45 3.225
655
DBT084 Diabetes Mellitus, Ketosis-Prone 60 3.221
656
P OVR046 Ovarian Cyst 46 3.215
657
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 3.211
658
c SML038 Small Cell Cancer of the Lung 69 3.210
659
c HMP029 Hemophilia a 68 3.207
660
P VNW001 Von Willebrand's Disease 65 3.204
661
MCR011 Microinvasive Gastric Cancer 41 3.185
662
c SCL052 Scleroderma, Familial Progressive 61 3.175
663
c ACT135 Acute Graft Versus Host Disease 51 3.174
664
P CTN015 Cutaneous T Cell Lymphoma 48 3.173
665
BCT002 Bacterial Vaginosis 53 3.157
666
TRY001 Trypanosomiasis 50 3.157
667
VRL011 Viral Infectious Disease 61 3.154
668
STT001 Status Epilepticus 59 3.153
669
HRT015 Heritable Pulmonary Arterial Hypertension 46 3.151
670
P CYS018 Cystitis 59 3.151
671
HMX003 Heme Oxygenase 1 Deficiency 27 3.147
672
GST019 Gastrointestinal Stromal Tumor 78 3.146
673
DSS008 Disease of Mental Health 74 3.145
674
P LYM033 Lymphoproliferative Syndrome 59 3.143
675
SDD001 Sudden Infant Death Syndrome 60 3.142
676
HDN002 Head Injury 44 3.137
677
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 3.133
678
CHL079 Children's Interstitial Lung Disease 26 3.130
679
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.126
680
P NJM001 Nijmegen Breakage Syndrome 76 3.126
681
HGH043 High Grade Glioma 45 3.120
682
PST048 Postural Orthostatic Tachycardia Syndrome 46 3.115
683
P TXP001 Toxoplasmosis 60 3.112
684
c DRM040 Dermatitis Herpetiformis, Familial 35 3.109
685
P DRM007 Dermatitis Herpetiformis 54 3.109
686
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 3.105
687
P PRS038 Personality Disorder 65 3.103
688
OVR094 Ovarian Epithelial Cancer 39 3.100
689
LPT001 Leptospirosis 66 3.099
690
PLY150 Polykaryocytosis Inducer 29 3.096
691
P CNJ013 Conjunctivitis 66 3.093
692
MCK029 Meckel Diverticulum 38 3.085
693
INT007 Intermediate Coronary Syndrome 54 3.083
694
c ACQ010 Acquired Polycythemia 46 3.083
695
TLR001 Tularemia 56 3.082
696
CTS005 Catastrophic Antiphospholipid Syndrome 43 3.081
697
CHR005 Chorioamnionitis 50 3.080
698
THY030 Thyroid Gland Disease 50 3.080
699
PST010 Pasteurellosis 39 3.080
700
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 3.079
701
c JVN010 Juvenile Rheumatoid Arthritis 66 3.071
702
SLP001 Sleeping Sickness 56 3.066
703
P DRM053 Dermatitis, Atopic 65 3.065
704
DSS009 Disseminated Intravascular Coagulation 57 3.062
705
FTL006 Fetal Alcohol Spectrum Disorder 43 3.060
706
ARG006 Aregenerative Anemia 28 3.059
707
BRN009 Burning Mouth Syndrome 51 3.059
708
PLS011 Plasmacytoma 56 3.059
709
VCC001 Vaccinia 47 3.057
710
CLR109 Colorectal Adenocarcinoma 50 3.056
711
MNK001 Menkes Disease 64 3.053
712
BBN001 Bubonic Plague 40 3.035
713
P HRD086 Hereditary Hypophosphatemic Rickets 40 3.035
714
P NSP012 Nasopharyngeal Carcinoma 61 3.028
715
END057 Endometrial Cancer 72 3.023
716
TRN072 Transferrin Serum Level Quantitative Trait Locus 2 17 3.023
717
P ART021 Arteriosclerosis 54 3.020
718
P SYS005 Systemic Scleroderma 74 3.016
719
c ATS210 Autosomal Recessive Sideroblastic Anemia 29 3.014
720
TRC012 Trichuriasis 43 3.012
721
P ALP009 Alopecia Areata 59 3.012
722
CCC002 Coccidiosis 50 3.006
723
SCR001 Secretory Meningioma 40 3.004
724
LYM002 Lymphoplasmacyte-Rich Meningioma 35 3.004
725
THY029 Thyroid Carcinoma 51 3.001
726
ALL010 Allergic Contact Dermatitis 56 2.998
727
P HYP083 Hypopituitarism 52 2.993
728
CHR066 Chronic Fatigue Syndrome 60 2.991
729
INF034 Infective Endocarditis 54 2.990
730
PRP083 Porphyria, Acute Intermittent 65 2.989
731
P LCH002 Lichen Planus 54 2.989
732
NRM001 Neuromyelitis Optica 61 2.987
733
c HRD010 Hereditary Spastic Paraplegia 66 2.982
734
P ATX030 Ataxia-Telangiectasia 80 2.965
735
MDD011 Mood Disorder 62 2.961
736
P RTT002 Rett Syndrome 79 2.958
737
AMN006 Aminoaciduria 37 2.956
738
P TCD001 Tic Disorder 49 2.955
739
YLL002 Yellow Fever 61 2.950
740
P FNC004 Fanconi Syndrome 60 2.947
741
MDD018 Middle East Respiratory Syndrome 44 2.944
742
ALP103 Alpha-1-Antitrypsin Deficiency 68 2.928
743
P CHR012 Chronic Granulomatous Disease 69 2.928
744
DBT010 Diabetic Neuropathy 54 2.927
745
MCR004 Macroglobulinemia 49 2.921
746
P SHR001 Short Bowel Syndrome 53 2.921
747
P INT070 Intestinal Obstruction 57 2.920
748
P SCL018 Scoliosis 57 2.901
749
PYR009 Pyridoxine Deficiency Anemia 35 2.898
750
SBC016 Subacute Delirium 43 2.896
751
HST011 Histoplasmosis 55 2.894
752
CLC001 Calciphylaxis 51 2.891
753
P HYP265 Hypotonia 42 2.886
754
P ALP061 Alopecia, Androgenetic, 1 49 2.885
755
PLS032 Plasmodium Falciparum Blood Infection Level 21 2.884
756
NPH009 Nephrolithiasis 54 2.880
757
INT075 Intracranial Hypertension 53 2.877
758
P EPD016 Epidermolysis Bullosa 53 2.867
759
P FML011 Familial Adenomatous Polyposis 71 2.861
760
PRC002 Paracoccidioidomycosis 54 2.860
761
P FTL001 Fetal Alcohol Syndrome 55 2.856
762
P OPT006 Optic Nerve Disease 58 2.851
763
P RHB003 Rhabdomyosarcoma 66 2.850
764
CHL056 Cheilitis 46 2.847
765
AND005 Androgen Insensitivity Syndrome, Mild 21 2.847
766
HYD038 Hydrops Fetalis, Nonimmune 59 2.844
767
PRT019 Protein-Losing Enteropathy 45 2.842
768
c MCL013 Mucolipidosis Iv 65 2.840
769
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 2.840
770
ENT004 Enthesopathy 51 2.834
771
MRS001 Marasmus 42 2.831
772
ORL015 Oral Squamous Cell Carcinoma 43 2.830
773
SXL003 Sexual Disorder 49 2.823
774
CLL003 Cellulitis 53 2.812
775
P MMB011 Membranous Nephropathy 50 2.805
776
c INF071 Inflammatory Bowel Disease 1 65 2.803
777
RTN020 Retinal Vascular Disease 46 2.799
778
HRN029 Hearing Loss, Noise-Induced 37 2.797
779
ASP004 Asphyxia Neonatorum 50 2.791
780
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 2.787
781
CST005 Castleman Disease 56 2.776
782
HST010 Histiocytosis 49 2.772
783
c SCN036 Secondary Progressive Multiple Sclerosis 55 2.770
784
AND014 Androgenic Alopecia 47 2.765
785
GRW007 Growth Hormone Deficiency 46 2.763
786
HPT067 Hepatocellular Adenoma 43 2.761
787
ASC010 Ascaris Lumbricoides Infection 49 2.761
788
P EYD002 Eye Disease 57 2.751
789
BCK006 Back Pain 47 2.746
790
PRP080 Peripheral Artery Disease 54 2.741
791
ANG061 Angular Cheilitis 28 2.739
792
ILT001 Ileitis 48 2.732
793
TST014 Testicular Cancer 52 2.728
794
INT066 Interstitial Lung Disease 60 2.724
795
OBS002 Obsessive-Compulsive Disorder 68 2.723
796
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 2.713
797
PTT009 Pituitary Gland Disease 53 2.710
798
P MYC033 Myoclonus 47 2.709
799
CRT013 Carotid Stenosis 51 2.705
800
LMB062 Limb Ischemia 55 2.701
801
PLC007 Placental Abruption 47 2.701
802
MCS002 Mucositis 56 2.689
803
HYP043 Hyperandrogenism 48 2.678
804
ATN005 Autonomic Dysfunction 46 2.677
805
GLM044 Glomerular Disease 35 2.674
806
RNL077 Renal Fibrosis 46 2.672
807
P GRV001 Graves' Disease 55 2.672
808
SPN051 Spondylitis 51 2.670
809
PPL021 Papilledema 49 2.670
810
P RTN024 Retinoblastoma 73 2.661
811
P OBS001 Obstructive Jaundice 48 2.658
812
ACT119 Acute Promyelocytic Leukemia 62 2.657
813
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 2.657
814
P PLY014 Polycystic Kidney Disease 69 2.656
815
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.652
816
CLR030 Clear Cell Renal Cell Carcinoma 54 2.650
817
PRT094 Protoporphyria, Erythropoietic, X-Linked 27 2.647
819
HMN047 Human Cytomegalovirus Infection 57 2.638
820
BRN002 Bronchiolitis 57 2.637
821
P RST002 Restrictive Cardiomyopathy 54 2.637
822
PLM010 Pulmonary Edema 55 2.637
823
P DYS021 Dysautonomia 38 2.637
824
P ANR048 Aniridia 1 64 2.634
825
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.626
826
c LKM005 Leukemia, T-Cell, Chronic 34 2.626
827
P ENC004 Encephalitis 61 2.623
828
KRT009 Keratosis 53 2.618
829
NRL004 Neuroleptic Malignant Syndrome 52 2.615
830
CRD132 Cardiac Conduction Defect 60 2.611
831
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 2.611
832
P PLY019 Polyneuropathy 52 2.610
833
c CNT035 Central Nervous System Disease 54 2.609
834
SPR032 Superficial Siderosis of the Central Nervous System 23 2.608
835
P AXN001 Axonal Neuropathy 35 2.607
836
HYP014 Hyperuricemia 51 2.602
837
CVR006 Cavernous Hemangioma 51 2.601
838
P RTN022 Retinal Vein Occlusion 54 2.601
839
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 2.599
840
PPT001 Peptic Esophagitis 52 2.599
841
P HML001 Hemolytic-Uremic Syndrome 52 2.598
842
ABT001 Abetalipoproteinemia 68 2.594
843
P SML001 Small Cell Carcinoma 52 2.594
844
CNT057 Central Centrifugal Cicatricial Alopecia 36 2.593
845
c BSL007 Basal Cell Carcinoma 68 2.583
846
PNC129 Pancreatic Adenocarcinoma 65 2.582
847
TLG001 Telogen Effluvium 31 2.579
848
OVR063 Overnutrition 42 2.576
849
ACT003 Acute Kidney Tubular Necrosis 46 2.573
850
c ACT004 Acute Diarrhea 40 2.573
851
CHY002 Chylomicron Retention Disease 64 2.560
852
CHR178 Chromosomal Triplication 34 2.560
853
CRC021 Carcinosarcoma 64 2.559
854
ALL003 Allergic Rhinitis 67 2.558
855
INT051 Intussusception 52 2.551
856
CNT016 Central Retinal Vein Occlusion 54 2.546
857
LYM017 Lyme Disease 62 2.543
858
P MDL005 Medulloblastoma 75 2.539
859
VGN023 Vaginitis 56 2.539
860
BRN012 Bronchiolitis Obliterans 56 2.533
861
FNG017 Fungal Infectious Disease 54 2.532
862
ACT017 Acute Chest Syndrome 50 2.521
863
VTM033 Vitamin K Deficiency Bleeding 48 2.519
864
P CHR285 Chronic Myelomonocytic Leukemia 60 2.518
865
HRY003 Hairy Cell Leukemia 61 2.518
866
CHL067 Cholecystitis 60 2.517
867
IMM003 Immunoglobulin Alpha Deficiency 44 2.513
868
MNT001 Mantle Cell Lymphoma 67 2.510
869
EWN003 Ewing Sarcoma 70 2.508
870
P GLY013 Glycogen Storage Disease 60 2.507
871
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 50 2.507
872
LYS002 Lysosomal Storage Disease 51 2.505
873
c BCT013 Bacterial Pneumonia 48 2.502
874
ALL006 Allergic Asthma 56 2.502
875
P FML340 Familial Episodic Pain Syndrome 50 2.500
876
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 2.490
877
P BLP003 Blepharospasm 46 2.478
878
c SVR005 Severe Pre-Eclampsia 50 2.478
879
INT002 Intermittent Claudication 61 2.477
880
PYR016 Pyridoxine Deficiency 29 2.475
881
BNG077 Benign Idiopathic Neonatal Seizures 23 2.468
882
MSC157 Muscular Dystrophy, Duchenne Type 79 2.464
883
c BCT007 Bacterial Meningitis 55 2.457
884
P CHN059 Chondrocalcinosis 52 2.450
885
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 2.448
886
c MJR022 Major Affective Disorder 8 38 2.447
887
c MJR024 Major Affective Disorder 9 41 2.447
888
P BPL003 Bipolar Disorder 56 2.447
889
P MMP001 Mumps 57 2.447
890
SPS019 Spastic Paraparesis 38 2.447
891
PNG002 Pain Agnosia 51 2.437
892
CRD137 Cardiogenic Shock 56 2.436
893
c PLM128 Pulmonary Hypertension, Primary, 2 28 2.433
894
MLT116 Multiple System Atrophy, Parkinsonian Type 29 2.429
895
PNM005 Pneumonic Plague 47 2.429
896
P MCR010 Microcephaly 60 2.427
897
CHR177 Chromophobe Renal Cell Carcinoma 54 2.416
898
P BRB001 Beriberi 44 2.415
899
c SPN225 Spondyloarthropathy 1 70 2.411
900
END011 Endometriosis of Ovary 39 2.410
901
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 2.406
902
ORL013 Oral Lichen Planus 46 2.405
903
P SJG008 Sjogren Syndrome 61 2.396
904
PTZ001 Peutz-Jeghers Syndrome 70 2.395
905
CRD223 Cardiac Arrhythmia 63 2.391
906
P TYR004 Tyrosinemia 50 2.391
907
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.391
908
LGN006 Legionnaire Disease 52 2.390
909
FRN006 Frontotemporal Dementia 68 2.388
910
NRM005 Neuromuscular Disease 63 2.382
911
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.382
912
P ADL017 Adult T-Cell Leukemia 56 2.382
913
P UVT001 Uveitis 57 2.377
914
AZS001 Azoospermia 45 2.375
915
PRS045 Prostatic Hypertrophy 53 2.374
916
CHL061 Childhood Leukemia 47 2.372
917
CRY036 Cryptogenic Cirrhosis 36 2.370
918
P MCL001 Mucolipidosis 49 2.370
919
P MTC133 Mitochondrial Myopathy 50 2.370
920
ACT228 Acute Radiation Syndrome 30 2.369
921
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 2.369
922
c HMG029 Hemoglobin Se Disease 40 2.362
923
PLM151 Pulmonary Arteriovenous Fistulas 35 2.360
924
BCT004 Bacteriuria 47 2.358
925
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 2.354
927
LPM012 Lipomatosis, Multiple 60 2.350
928
PLM005 Pleomorphic Lipoma 40 2.350
929
c PRM108 Primary Progressive Multiple Sclerosis 51 2.346
930
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.340
931
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.340
932
ING001 Inguinal Hernia 59 2.340
933
WDH003 Woodhouse-Sakati Syndrome 40 2.340
934
c DRR009 Diarrhea 6 45 2.338
935
CMM005 Common Cold 56 2.335
936
PLC005 Placental Insufficiency 56 2.333
937
BRN032 Brain Glioma 45 2.331
938
TRC022 Tricuspid Valve Insufficiency 47 2.329
939
HMR039 Hemorrhage, Intracerebral 57 2.329
940
P NRV007 Nervous System Disease 67 2.326
941
PRS021 Prostatic Adenoma 43 2.325
942
P MJR001 Major Depressive Disorder 68 2.323
943
KWS002 Kawasaki Disease 65 2.323
944
KRT006 Keratoconjunctivitis 53 2.322
945
c ERL056 Early-Onset Parkinson's Disease 40 2.321
946
P ANT006 Antiphospholipid Syndrome 55 2.314
947
CHR682 Chronic Bilirubin Encephalopathy 37 2.314
948
P TMP001 Temporal Lobe Epilepsy 49 2.314
949
FSC002 Fascioliasis 44 2.313
950
P PLM006 Pulmonary Alveolar Proteinosis 53 2.308
951
P ACR106 Acrocephalopolysyndactyly Type Iii 37 2.307
952
c FNC025 Fanconi Anemia, Complementation Grou