Search results for Succinic acid

1753 hits were found for Succinic acid

# Family MCID Name MIFTS Score
1
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 58.789
2
LPD008 Lipid Metabolism Disorder 62 39.375
3
NNL005 Non-Alcoholic Fatty Liver Disease 63 37.868
4
FTT001 Fatty Liver Disease 62 36.287
5
MTC207 Mitochondrial Complex Ii Deficiency, Nuclear Type 1 55 35.729
6
GST092 Gastroesophageal Reflux 61 35.489
7
RPD005 Rapidly Involuting Congenital Hemangioma 46 35.164
8
CHL068 Cholestasis 61 34.700
9
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 56 33.543
10
P MPL001 Maple Syrup Urine Disease 70 32.770
11
P NRB001 Neuroblastoma 66 29.653
12
HLX001 Helix Syndrome 48 29.608
13
MTB004 Metabolic Acidosis 48 28.928
14
RFS006 Refsum Disease, Classic 63 28.843
15
ARG002 Argininosuccinic Aciduria 61 28.355
16
P LVR013 Liver Disease 69 28.231
17
NRL016 Neural Tube Defects 81 26.779
18
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 26.709
19
CLT003 Colitis 63 26.500
20
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 26.126
21
GT001 Gout 64 26.041
22
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 25.814
23
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 25.814
24
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 25.812
25
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 25.812
26
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 25.807
27
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 25.807
28
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 25.807
29
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 25.807
30
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 25.807
31
c TYP009 Type 2 Diabetes Mellitus 92 25.444
32
48X005 48,xyyy 39 25.396
33
P SZR006 Seizure Disorder 70 25.366
34
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 25.216
35
HYP066 Hyperglycemia 61 24.730
36
LVR012 Liver Cirrhosis 63 24.283
37
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 24.229
38
ISC004 Ischemia 61 24.154
39
ACT119 Acute Promyelocytic Leukemia 62 23.738
40
HYP266 Hypoxia 57 23.702
41
P DDN001 Duodenal Ulcer 53 23.577
42
AMN002 Amino Acid Metabolic Disorder 39 23.379
43
AGN016 Aging 54 23.296
44
BNR002 Bone Resorption Disease 47 23.175
45
ALK013 Alkaptonuria 59 23.133
46
c MTC059 Mitochondrial Dna Depletion Syndrome 5 48 23.118
47
P HYP750 Hypertriglyceridemia, Familial 62 22.816
48
P ENC018 Encephalopathy 62 22.806
49
P CRN300 Coronary Heart Disease 1 73 22.780
50
P MYP004 Myopathy 67 22.775
51
c HYP836 Hypercholesterolemia, Familial, 1 73 22.605
52
GLL048 Glial Tumor 52 22.446
53
HYP781 Hypoascorbemia 52 22.394
54
GLM045 Glioma 63 22.352
55
ULC004 Ulcerative Colitis 74 22.215
56
ISV001 Isovaleric Acidemia 54 22.202
57
P PHC003 Pheochromocytoma 69 22.182
58
NNL006 Non-Alcoholic Steatohepatitis 54 22.120
59
OST012 Osteoarthritis 77 21.577
60
ADR040 Adrenal Gland Pheochromocytoma 46 21.568
61
P DBT009 Diabetes Mellitus 67 21.552
62
c CHR684 Chronic Kidney Disease 69 21.552
63
IRN002 Iron Metabolism Disease 57 21.372
64
P KDN018 Kidney Disease 72 21.350
65
P BRS047 Breast Cancer 98 21.314
66
P DRR001 Diarrhea 55 21.229
67
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 21.201
68
PPT005 Peptic Ulcer Disease 58 21.143
69
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 21.021
70
PRM236 Primary Biliary Cholangitis 60 20.748
71
GLB002 Glioblastoma 67 20.663
72
P GST044 Gastritis 55 20.553
73
HYP056 Hypoglycemia 65 20.531
74
HMN044 Human Immunodeficiency Virus Type 1 78 20.518
75
P LKM002 Leukemia 67 20.427
76
PRT037 Pertussis 65 20.403
77
ALL029 Allergic Disease 59 20.394
78
P URN019 Urinary Tract Infection 49 20.389
79
P ACN011 Acne 57 20.359
80
ORG002 Organic Acidemia 44 20.346
81
P HNT016 Huntington Disease 73 20.196
82
ATH013 Atherosclerosis Susceptibility 63 20.111
83
MNT002 Mental Depression 57 20.103
84
GBM001 Gaba Aminotransferase Deficiency 29 20.094
85
DFC004 Deficiency Anemia 74 20.082
86
P PRS040 Prostate Cancer 95 20.045
87
PHS025 Phosphatase, Acid, of Tissues 28 19.770
88
DPR016 Depression 65 19.626
89
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 19.572
90
CYS001 Cystic Fibrosis 78 19.559
91
P CLR023 Colorectal Cancer 100 19.519
92
P LCT001 Lactic Acidosis 51 19.452
93
P HPT023 Hepatocellular Carcinoma 96 19.361
94
c HYP595 Hypertension, Essential 85 19.291
95
P HRT032 Heart Disease 81 19.155
96
P EPL164 Epilepsy 68 19.110
97
47X002 47,xyy 48 18.984
98
P OST002 Osteoporosis 76 18.930
99
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 18.899
100
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 18.899
101
P INF038 Influenza 68 18.782
102
CRH001 Crohn's Disease 80 18.782
103
P INF037 Inflammatory Bowel Disease 53 18.720
104
c MGR028 Migraine with or Without Aura 1 64 18.623
105
HYP060 Hyperinsulinism 54 18.609
106
P ART022 Arthritis 71 18.605
107
P PRD008 Periodontitis 64 18.579
108
LPP008 Lipoprotein Quantitative Trait Locus 65 18.571
109
P MJR001 Major Depressive Disorder 68 18.543
110
P ALZ034 Alzheimer Disease 87 18.516
111
PHN003 Phenylketonuria 76 18.397
112
NPH009 Nephrolithiasis 54 18.277
113
P PRG013 Paraganglioma 57 18.239
114
c INH020 Inherited Metabolic Disorder 48 18.207
115
RNL114 Renal Cell Carcinoma, Nonpapillary 80 18.062
116
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 18.051
117
HRW001 Hair Whorl 35 17.991
118
P MYC084 Mycobacterium Tuberculosis 1 68 17.958
119
P HPT021 Hepatitis 69 17.932
120
HMC014 Homocysteinemia 52 17.916
121
STT001 Status Epilepticus 59 17.872
122
P PNC035 Pancreatic Cancer 86 17.870
123
c PRC016 Pre-Eclampsia 65 17.833
124
P LNG032 Lung Cancer 98 17.746
125
c ACT068 Acute Cystitis 61 17.586
126
GST023 Gastric Ulcer 52 17.544
127
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 17.473
128
IMM167 Immune Deficiency Disease 78 17.367
129
GBT001 Gaba-Transaminase Deficiency 37 17.357
130
ADN018 Adenoma 59 17.287
131
SPN186 Spinal Cord Injury 61 17.178
132
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 17.128
133
c ACT071 Acute Kidney Failure 60 17.104
134
P BPL003 Bipolar Disorder 56 17.097
135
CYT002 Cytokine Deficiency 43 17.026
136
c MJR022 Major Affective Disorder 8 38 16.998
137
c MJR024 Major Affective Disorder 9 41 16.998
138
P VSC007 Vascular Disease 63 16.995
139
ART140 Arteries, Anomalies of 53 16.933
140
P HYP265 Hypotonia 42 16.892
141
ADR007 Adrenoleukodystrophy 73 16.875
142
c ACT027 Acute Pancreatitis 60 16.804
143
c LKM061 Leukemia, Acute Myeloid 83 16.792
144
P PSR002 Psoriasis 63 16.787
145
DRM006 Dermatitis 62 16.725
146
P NRP001 Neuropathy 60 16.690
147
OCL069 Ocular Motor Apraxia 57 16.681
148
OST159 Osteogenic Sarcoma 66 16.644
149
CTR172 Citrullinemia, Classic 65 16.612
150
P HRP006 Herpes Simplex 65 16.594
151
BRN071 Brain Injury 50 16.591
152
TRM010 Traumatic Brain Injury 51 16.578
153
P CHL066 Cholangitis 52 16.574
154
ANX004 Anoxia 40 16.445
155
P RHM011 Rheumatoid Arthritis 82 16.409
156
TRC120 Tricarboxylic Acid Cycle, Defect of 16 16.257
157
GMM004 Gamma-Amino Butyric Acid Metabolism Disorder 27 16.254
158
PPL052 Papillomatosis, Confluent and Reticulated 34 16.238
159
c HPT073 Hepatitis C Virus 71 16.185
160
P ATS364 Autism 69 16.177
161
CNG034 Congestive Heart Failure 69 16.165
162
c TYP008 Type 1 Diabetes Mellitus 70 16.149
163
KRT002 Keratomalacia 55 16.141
164
P PNC044 Pancreatitis 61 16.140
165
c ATS007 Autism Spectrum Disorder 72 16.113
166
HPT004 Hepatic Coma 43 16.107
167
PST011 Pustulosis of Palm and Sole 52 16.058
168
ALC007 Alcohol Dependence 66 16.037
169
P MYL006 Myeloid Leukemia 61 15.969
170
BCT022 Bacterial Infectious Disease 56 15.943
171
P MYC007 Myocardial Infarction 70 15.904
172
CHL014 Cholera 62 15.889
173
PRT036 Peritonitis 65 15.885
174
HPT019 Hepatic Encephalopathy 59 15.877
175
P ADN016 Adenocarcinoma 63 15.811
176
HMP009 Haemophilus Influenzae 41 15.808
177
SCC003 Succinic Acidemia 10 15.739
178
STR067 Stroke, Ischemic 80 15.725
179
MYL069 Myeloma, Multiple 77 15.711
180
P OVR042 Ovarian Cancer 88 15.700
181
c AMY091 Amyotrophic Lateral Sclerosis 1 88 15.657
182
P GST053 Gastric Cancer 83 15.625
183
SKN016 Skin Disease 63 15.583
184
c PCH010 Pachyonychia Congenita 3 43 15.552
185
P BND020 Bone Disease 59 15.549
186
MYP097 Myopathy with Lactic Acidosis, Hereditary 31 15.537
187
P LTR001 Lateral Sclerosis 58 15.357
188
TXC005 Toxic Shock Syndrome 62 15.337
189
c MCR120 Microvascular Complications of Diabetes 7 47 15.303
190
ATM095 Autoimmune Disease 61 15.232
191
END086 End Stage Renal Disease 52 15.221
192
c DNT047 Dentinogenesis Imperfecta Type 2 35 15.209
193
ATS010 Autosomal Recessive Disease 42 15.177
194
PLM001 Pulmonary Tuberculosis 69 15.173
195
c MCR113 Microvascular Complications of Diabetes 3 52 15.167
196
PRT251 Proteinuria, Chronic Benign 57 15.134
197
c HPT001 Hepatitis C 62 15.127
198
c MCR133 Microvascular Complications of Diabetes 4 41 14.990
199
INS024 Insulin-Like Growth Factor I 78 14.989
200
c MCR130 Microvascular Complications of Diabetes 6 41 14.985
201
c ATR087 Atrial Standstill 1 74 14.978
202
c HPT016 Hepatitis B 62 14.929
203
P HYP086 Hypothyroidism 69 14.893
204
GYR004 Gyrate Atrophy of Choroid and Retina 58 14.891
205
c VSC019 Vesicoureteral Reflux 1 57 14.812
206
URL001 Urolithiasis 46 14.740
207
GLC003 Glucose Intolerance 54 14.724
208
CRV035 Cervical Cancer 73 14.712
209
P MLN008 Melanoma 76 14.685
210
P GLM040 Glioma Susceptibility 1 71 14.682
211
CNS004 Constipation 56 14.639
212
URT049 Urate Oxidase, Pseudogene 24 14.585
213
P BLD134 Bladder Cancer 79 14.506
214
VTM002 Vitamin B12 Deficiency 48 14.354
215
c MCR115 Microvascular Complications of Diabetes 5 65 14.338
216
CHL123 Chlamydia 58 14.306
217
SVR001 Severe Acute Respiratory Syndrome 67 14.284
218
ADR022 Adrenomyeloneuropathy 39 14.256
219
P PRK039 Parkinsonism 55 14.245
220
DNT012 Dental Caries 53 14.174
221
P OVR082 Overgrowth Syndrome 49 14.112
222
P ADL010 Adult Respiratory Distress Syndrome 71 14.099
223
P DRM053 Dermatitis, Atopic 65 14.014
224
P MSC003 Muscular Atrophy 52 13.990
225
URM002 Uremia 47 13.981
226
ESP021 Esophageal Cancer 83 13.936
227
P SCH015 Schizophrenia 74 13.845
228
AMN012 Aminoacidopathies 20 13.804
229
RCK004 Rickets 68 13.793
230
MTH071 Methane Production 25 13.732
231
STM007 Stomatitis 54 13.672
232
NPH091 Nephrolithiasis, Calcium Oxalate 61 13.583
233
CRB004 Cerebral Artery Occlusion 45 13.582
234
P BCL017 B-Cell Lymphoma 59 13.579
235
P INF032 Infertility 57 13.578
236
DBT010 Diabetic Neuropathy 54 13.570
237
PLM129 Pulmonary Disease, Chronic Obstructive 74 13.557
238
c SML038 Small Cell Cancer of the Lung 69 13.527
239
HLC007 Helicobacter Pylori Infection 67 13.491
240
P ENC004 Encephalitis 61 13.490
241
P MLT020 Multiple Sclerosis 79 13.450
243
VCC001 Vaccinia 47 13.394
244
THY029 Thyroid Carcinoma 51 13.386
245
BRN024 Bronchitis 67 13.354
246
P PRP019 Peripheral Nervous System Disease 58 13.265
247
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 13.246
248
LWC001 Low Compliance Bladder 45 13.224
249
P MSC005 Muscular Dystrophy 67 13.218
250
P MTH008 Methylmalonic Acidemia 52 13.205
251
P ALC033 Alcohol Use Disorder 61 13.132
252
SJG002 Sjogren-Larsson Syndrome 54 13.119
253
CRB039 Cerebrovascular Disease 66 13.104
254
c HPT003 Hepatitis a 63 13.050
255
DWN001 Down Syndrome 70 12.945
256
SPN035 Spindle Cell Sarcoma 54 12.881
257
LNG099 Lung Disease 62 12.879
258
SRC014 Sarcoma 65 12.872
259
P RHN004 Rhinitis 57 12.850
260
P RSP003 Respiratory Failure 74 12.835
261
P SKN015 Skin Carcinoma 71 12.798
262
P GLM007 Glomerulonephritis 60 12.786
263
SQM006 Squamous Cell Carcinoma 60 12.719
264
TTN003 Tetanus 65 12.685
265
OST003 Osteonecrosis 61 12.606
266
P ATT013 Attention Deficit-Hyperactivity Disorder 64 12.556
267
EMB004 Embryonal Carcinoma 56 12.529
268
MLG169 Malignant Astrocytoma 57 12.526
269
GST045 Gastroenteritis 58 12.503
270
P AST005 Asthma 76 12.462
271
HYP005 Hypokalemia 55 12.445
272
CLN015 Colon Adenocarcinoma 65 12.432
273
P LKM062 Leukemia, Acute Lymphoblastic 69 12.422
274
KRT009 Keratosis 53 12.416
275
ZLL002 Zollinger-Ellison Syndrome 55 12.373
276
DSS032 Disease by Infectious Agent 55 12.292
277
P ZLL001 Zellweger Syndrome 65 12.291
278
MLR004 Malaria 80 12.248
279
P CTR002 Cataract 60 12.238
280
CRD132 Cardiac Conduction Defect 60 12.226
281
P TRM003 Tremor 48 12.214
282
P ATR011 Atrial Fibrillation 66 12.159
283
P LPS004 Lupus Erythematosus 61 12.150
284
P RTN024 Retinoblastoma 73 12.072
285
P HDC001 Headache 57 12.069
286
c ACT075 Acute Myocardial Infarction 56 12.064
287
P PLY019 Polyneuropathy 52 12.052
288
P EXN002 Exanthem 58 12.045
289
c SYS001 Systemic Lupus Erythematosus 87 12.016
290
PRS045 Prostatic Hypertrophy 53 11.998
291
P GLY013 Glycogen Storage Disease 60 11.996
292
P THR014 Thrombocytopenia 66 11.970
293
ACQ007 Acquired Immunodeficiency Syndrome 59 11.882
294
P BRS044 Breast Adenocarcinoma 58 11.875
295
P PYL005 Pyelonephritis 57 11.861
296
P INB001 Inborn Amino Acid Metabolism Disorder 11 11.825
297
GST033 Gestational Diabetes 61 11.824
298
P DYS154 Dystonia 64 11.811
299
P KDN017 Kidney Cancer 61 11.779
300
P AMY004 Amyloidosis 70 11.760
301
c DWL002 Dowling-Degos Disease 1 58 11.739
302
P HYP076 Hyperthyroidism 53 11.733
303
GST019 Gastrointestinal Stromal Tumor 78 11.717
304
SVR004 Severe Combined Immunodeficiency 72 11.716
305
PLM010 Pulmonary Edema 55 11.699
306
P FBR017 Fibrosarcoma 56 11.698
307
CYS013 Cystinuria 66 11.672
308
HGH043 High Grade Glioma 45 11.641
309
PRP001 Propionic Acidemia 65 11.639
310
AVN001 Avian Influenza 61 11.618
311
P PNM007 Pneumonia 67 11.535
312
NRR001 Neuroretinitis 42 11.499
313
RTN023 Retinitis 46 11.497
314
P LNG064 Lung Cancer Susceptibility 3 70 11.486
315
IRN001 Iron Deficiency Anemia 58 11.474
316
MDD011 Mood Disorder 62 11.466
317
HMS001 Hemosiderosis 48 11.465
318
MTH009 Mouth Disease 57 11.439
319
P ECL001 Eclampsia 52 11.355
320
P ART021 Arteriosclerosis 54 11.347
321
P FRG001 Fragile X Syndrome 70 11.343
322
CHL004 Cholelithiasis 49 11.291
323
CLF027 Cleft Palate, Isolated 64 11.287
324
ALL014 Allergic Encephalomyelitis 34 11.240
325
IRR002 Irritable Bowel Syndrome 65 11.239
326
MYL009 Myelodysplastic Syndrome 67 11.198
327
PRS021 Prostatic Adenoma 43 11.157
328
PRS047 Prostatitis 58 11.154
329
P PRP029 Porphyria 60 11.140
330
P EYD002 Eye Disease 57 11.134
331
DPH001 Diphtheria 59 11.123
332
ANG054 Angina Pectoris 66 11.109
333
c DLT002 Dilated Cardiomyopathy 78 11.065
334
P TMP001 Temporal Lobe Epilepsy 49 11.050
335
PLM033 Pulmonary Embolism 58 11.045
336
PRX001 Peroxisomal Disease 46 11.012
337
MYP009 Myopathy with Deficiency of Iscu 12 11.006
338
P NTR004 Neutropenia 63 10.948
339
PRP027 Peripheral Vascular Disease 71 10.947
340
P NRF002 Neurofibromatosis 57 10.937
341
P PLY011 Polycystic Ovary Syndrome 57 10.913
342
P PLM037 Pulmonary Hypertension 72 10.903
343
P NSP012 Nasopharyngeal Carcinoma 61 10.867
344
P KLZ004 Kala-Azar 1 41 10.855
345
LSH001 Leishmaniasis 64 10.855
346
PRS129 Prostatic Hyperplasia, Benign 49 10.844
347
P RRH023 Rare Hereditary Hemochromatosis 54 10.841
348
P HYP098 Hypereosinophilic Syndrome 66 10.837
349
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 10.819
350
P LYM118 Lymphoma 67 10.796
351
P NPH012 Nephrotic Syndrome 60 10.744
352
P PLM036 Pulmonary Fibrosis 66 10.728
353
c ACT134 Acute Liver Failure 59 10.717
354
PST092 Posttransplant Acute Limbic Encephalitis 28 10.704
355
ACY011 Acyl-Coa Dehydrogenase Deficiency 30 10.692
356
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 10.689
357
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 10.680
358
LPT014 Leptin Deficiency or Dysfunction 78 10.664
359
P MTC133 Mitochondrial Myopathy 50 10.654
360
P PRK057 Parkinson Disease, Late-Onset 80 10.614
361
P THL005 Thalassemia 56 10.565
362
P CRD119 Cardiac Arrest 67 10.553
363
P CYS018 Cystitis 59 10.515
364
P CRD246 Cardiovascular System Disease 56 10.514
365
P BNG032 Benign Mesothelioma 53 10.511
366
P HYP069 Hyperparathyroidism 62 10.510
367
BRN004 Brain Edema 54 10.510
368
P SPP010 Suppressor of Tumorigenicity 3 51 10.509
369
P RTN008 Retinitis Pigmentosa 80 10.501
370
NTR005 Nutritional Deficiency Disease 61 10.494
371
CRB011 Cerebrotendinous Xanthomatosis 65 10.452
372
P LKM071 Leukemia, Chronic Lymphocytic 75 10.400
373
GST050 Gastrointestinal System Disease 55 10.390
374
INS001 Insulinoma 59 10.380
375
PLY150 Polykaryocytosis Inducer 29 10.338
376
DYS073 Dysphagia 53 10.328
377
PPL022 Papilloma 53 10.320
378
c VRL010 Viral Hepatitis 53 10.311
379
P MLN007 Male Infertility 56 10.311
380
CNT047 Contact Dermatitis 57 10.285
381
CHG001 Chagas Disease 66 10.256
382
c ACT073 Acute Leukemia 58 10.240
383
P ALP008 Alopecia 54 10.217
384
ALL003 Allergic Rhinitis 67 10.172
385
ENT011 Enterocolitis 55 10.150
386
HNS001 Hansen's Disease 32 10.109
387
P DMN002 Dementia 66 10.107
388
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 10.106
389
BRN028 Brain Cancer 74 10.100
390
P URT039 Urticaria 58 10.081
391
P LPR021 Leprosy 3 71 10.066
392
HDN002 Head Injury 44 10.063
393
P CHR345 Chronic Pain 50 10.051
394
MST005 Mastitis 53 10.019
395
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 10.011
396
c BRN108 Branchiootic Syndrome 1 62 10.005
397
P PLY014 Polycystic Kidney Disease 69 9.977
398
P MNN013 Meningitis 65 9.967
399
ACT098 Acute Erythroid Leukemia 55 9.940
400
THR024 Thrombosis 56 9.938
401
SCH014 Schistosomiasis 56 9.928
402
SQM002 Squamous Cell Papilloma 46 9.927
403
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 9.922
404
END057 Endometrial Cancer 72 9.922
405
P MTC069 Mitochondrial Disorders 57 9.915
406
MSL001 Measles 61 9.905
407
PRP030 Purpura 54 9.843
408
INT323 Intraocular Pressure Quantitative Trait Locus 64 9.798
409
P HMC002 Homocystinuria 53 9.773
410
P MYC033 Myoclonus 47 9.773
411
NWC001 Newcastle Disease 47 9.770
412
c LKM063 Leukemia, Chronic Myeloid 71 9.761
413
P RTN016 Retinal Degeneration 52 9.731
414
GNG013 Gingivitis 59 9.712
415
TRT001 Teratocarcinoma 42 9.708
416
PNG002 Pain Agnosia 51 9.696
417
P HYP061 Hypertrophic Cardiomyopathy 69 9.694
418
P ATR005 Atrophic Gastritis 50 9.671
419
P RCT021 Rectum Cancer 54 9.595
420
ARG004 Argyria 26 9.545
421
P CND004 Candidiasis 58 9.542
422
P ART023 Arthropathy 61 9.538
423
STF001 Stiff-Person Syndrome 58 9.532
424
ADL002 Adult Syndrome 70 9.527
425
XNT003 Xanthomatosis 49 9.500
426
ANX010 Anxiety 70 9.492
427
c PRD040 Periodontitis, Chronic 52 9.482
428
P OBS001 Obstructive Jaundice 48 9.478
429
P INS002 in Situ Carcinoma 53 9.460
430
P SHR001 Short Bowel Syndrome 53 9.424
431
P TRN020 Turner Syndrome 67 9.409
432
BCT002 Bacterial Vaginosis 53 9.393
433
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 59 9.349
434
BLR008 Bilirubin Metabolic Disorder 57 9.249
435
MLD018 Mild Cognitive Impairment 48 9.234
436
P ANR048 Aniridia 1 64 9.220
437
CRV045 Cervical Intraepithelial Neoplasia 39 9.202
438
ORL015 Oral Squamous Cell Carcinoma 43 9.200
439
CRV002 Cervix Uteri Carcinoma in Situ 47 9.199
440
CVD001 Covid-19 57 9.194
441
RYS001 Reye Syndrome 49 9.177
442
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 9.141
443
ISL099 Isolated Methylmalonic Acidemia 36 9.140
444
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 9.124
445
c LKM005 Leukemia, T-Cell, Chronic 34 9.096
446
RNL077 Renal Fibrosis 46 9.092
447
P SCK005 Sickle Cell Disease 56 9.091
448
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 9.077
449
P CNJ013 Conjunctivitis 66 9.029
450
P MLT074 Multiple Endocrine Neoplasia 59 9.007
451
MDD018 Middle East Respiratory Syndrome 44 9.006
452
INT007 Intermediate Coronary Syndrome 54 8.941
453
VGN023 Vaginitis 56 8.924
454
CLR108 Colorectal Adenoma 64 8.854
455
LYS002 Lysosomal Storage Disease 51 8.820
456
CMM005 Common Cold 56 8.811
457
P SYS005 Systemic Scleroderma 74 8.782
458
HYD002 Hydronephrosis 58 8.776
459
BLR001 Biliary Atresia 55 8.774
460
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 8.765
461
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 65 8.747
462
ORL011 Oral Cancer 60 8.743
463
P INT068 Intestinal Disease 53 8.712
464
P RNL007 Renal Tubular Acidosis 50 8.710
465
c BSL007 Basal Cell Carcinoma 68 8.666
466
MSC007 Muscle Hypertrophy 64 8.663
467
SBC016 Subacute Delirium 43 8.660
468
MMM001 Mammary Paget's Disease 53 8.635
469
P ACT008 Actinic Keratosis 54 8.630
470
P HML002 Hemolytic Anemia 62 8.628
471
PSY004 Psychotic Disorder 66 8.623
472
P SLP005 Sleep Disorder 61 8.602
473
P MCR129 Microvascular Complications of Diabetes 1 68 8.583
474
P TYR004 Tyrosinemia 50 8.582
475
END040 Endogenous Depression 55 8.578
476
c PLM164 Pulmonary Hypertension, Primary, 1 76 8.574
477
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 8.545
478
P CLC063 Celiac Disease 1 66 8.496
479
IGR001 Ige Responsiveness, Atopic 59 8.482
480
P THY032 Thyroiditis 57 8.475
481
AMN006 Aminoaciduria 37 8.470
482
PLC002 Plica Syndrome 35 8.457
483
SYN007 Synovitis 55 8.457
484
P GRF003 Graft-Versus-Host Disease 71 8.439
485
SCR011 Scrapie 39 8.398
486
TRN015 Transient Cerebral Ischemia 63 8.389
487
P PTT006 Pituitary Adenoma 55 8.349
488
CHC001 Chickenpox 57 8.347
489
PTT037 Pituitary Tumors 44 8.346
490
NRT001 Neurotic Disorder 56 8.324
491
P MYC008 Myocarditis 59 8.317
492
TYP007 Typhoid Fever 64 8.305
493
BRK010 Burkitt Lymphoma 66 8.274
494
P FNC004 Fanconi Syndrome 60 8.266
495
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 8.223
496
TLN003 Telangiectasis 51 8.216
497
OTT002 Otitis Media 71 8.190
498
MSC157 Muscular Dystrophy, Duchenne Type 79 8.180
499
GST040 Gastric Adenocarcinoma 67 8.175
500
PRN011 Pernicious Anemia 53 8.164
501
CHR074 Choriocarcinoma 46 8.160
502
P MCR010 Microcephaly 60 8.146
503
LYM133 Lymphoma, Hodgkin, Classic 74 8.140
504
c SCL052 Scleroderma, Familial Progressive 61 8.132
505
PRN019 Perinatal Necrotizing Enterocolitis 60 8.119
506
DBT084 Diabetes Mellitus, Ketosis-Prone 60 8.094
507
FDL002 Food Allergy 47 8.074
508
PNC001 Pancytopenia 53 8.048
509
P SRC025 Sarcoidosis 1 71 8.022
510
CHL067 Cholecystitis 60 8.015
511
P FML011 Familial Adenomatous Polyposis 71 8.015
512
P PRN023 Prion Disease 60 8.015
513
SPS057 Spasticity 42 7.981
514
DYS015 Dysentery 50 7.962
515
PNC041 Pancreatic Ductal Adenocarcinoma 51 7.961
516
MTC005 Mitochondrial Metabolism Disease 45 7.948
517
PNC129 Pancreatic Adenocarcinoma 65 7.944
518
P END044 Endometriosis 62 7.936
519
RHB024 Rhabdomyosarcoma 2 67 7.928
520
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 7.923
521
MNN043 Meningioma, Familial 79 7.914
522
ASP036 Aspirin Allergy 27 7.911
523
P UVT001 Uveitis 57 7.906
524
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 7.899
525
P SCL018 Scoliosis 57 7.877
527
LYM019 Lymphosarcoma 46 7.850
528
P LKD001 Leukodystrophy 59 7.835
529
HYP141 Hyperphenylalaninemia 42 7.829
530
GTR002 Goiter 53 7.823
531
CRB037 Cerebral Palsy 67 7.800
532
P ANP001 Anaplastic Large Cell Lymphoma 61 7.782
533
PRT013 Portal Hypertension 59 7.781
534
GLT035 Glutaric Acidemia I 57 7.763
535
P RHB003 Rhabdomyosarcoma 66 7.763
536
c ACT042 Acute Pyelonephritis 45 7.752
537
SCR001 Secretory Meningioma 40 7.731
538
LYM002 Lymphoplasmacyte-Rich Meningioma 35 7.731
539
SPN021 Spinal Meningioma 50 7.731
540
ALL010 Allergic Contact Dermatitis 56 7.723
541
P HYD006 Hydrocephalus 61 7.690
542
P RTN018 Retinal Disease 53 7.682
543
KRN002 Kearns-Sayre Syndrome 63 7.664
544
P MVM001 Movement Disease 61 7.657
545
SCK003 Sickle Cell Anemia 74 7.656
546
AMN003 Amnestic Disorder 54 7.639
547
RTN017 Retinal Detachment 60 7.608
548
SPL018 Splenomegaly 49 7.607
549
MGL001 Megaloblastic Anemia 58 7.597
550
ANT039 Antisynthetase Syndrome 55 7.584
551
P SLP006 Sleep Apnea 69 7.557
552
P MDL005 Medulloblastoma 75 7.552
553
PLC008 Placenta Disease 49 7.545
554
c MST023 Mesothelioma, Malignant 56 7.538
555
ALL006 Allergic Asthma 56 7.527
556
P VSC011 Vasculitis 61 7.522
557
CRH005 Crohn's Colitis 53 7.511
558
NRN004 Neuroendocrine Tumor 59 7.509
559
PRT038 Protein-Energy Malnutrition 53 7.490
560
c SCN036 Secondary Progressive Multiple Sclerosis 55 7.479
561
P SBR004 Seborrheic Dermatitis 44 7.439
562
IGG001 Iga Glomerulonephritis 50 7.433
563
MLK006 Milk Allergy 47 7.409
564
LGH007 Leigh Syndrome 70 7.387
565
P END033 Endocarditis 58 7.383
566
ANT024 Anthrax Disease 58 7.377
567
DSS009 Disseminated Intravascular Coagulation 57 7.375
568
LYM143 Lymphoma, Non-Hodgkin, Familial 75 7.371
569
CLF001 Cleft Lip 53 7.339
570
CLR109 Colorectal Adenocarcinoma 50 7.333
571
VSC002 Vascular Dementia 60 7.307
572
RBS001 Rabies 58 7.303
573
P OPN001 Open-Angle Glaucoma 55 7.257
574
SLP001 Sleeping Sickness 56 7.240
575
c HNT011 Huntington Disease-Like 3 34 7.231
576
P GRV001 Graves' Disease 55 7.208
577
c BCT007 Bacterial Meningitis 55 7.194
578
RLP002 Relapsing-Remitting Multiple Sclerosis 56 7.157
579
PRP016 Paraplegia 52 7.148
580
VRC005 Varicose Veins 60 7.123
581
OST017 Osteomyelitis 63 7.120
582
URN010 Urinary Tract Obstruction 55 7.109
583
SQM013 Squamous Cell Carcinoma, Head and Neck 73 7.081
584
URT010 Ureteral Obstruction 45 7.078
585
PHR003 Pharyngitis 58 7.069
586
KRT006 Keratoconjunctivitis 53 7.051
587
PRP083 Porphyria, Acute Intermittent 65 7.041
588
PLM134 Pulmonary Fibrosis, Idiopathic 76 7.039
589
FBR047 Fibromyalgia 58 7.009
590
P ANG015 Angioedema 56 7.003
591
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 6.993
592
CHR073 Choreatic Disease 54 6.993
593
VSC003 Visceral Leishmaniasis 55 6.992
594
ANR007 Anorexia Nervosa 60 6.965
595
ACR007 Acromegaly 70 6.944
596
P SNS001 Sensorineural Hearing Loss 59 6.902
597
THY111 Thyroid Carcinoma, Familial Medullary 67 6.896
598
ANR040 Aneurysm 61 6.895
599
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 6.887
600
KRT019 Keratitis, Hereditary 66 6.869
601
TRN018 Transitional Cell Carcinoma 56 6.852
602
P SPN046 Spinal Muscular Atrophy 63 6.847
603
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 6.839
604
LWC002 Lowe Oculocerebrorenal Syndrome 68 6.836
605
P TBR001 Tuberous Sclerosis 69 6.827
606
GST030 Gastrinoma 45 6.805
607
TRY001 Trypanosomiasis 50 6.792
608
IMP005 Impotence 52 6.782
609
HPT022 Hepatoblastoma 54 6.775
610
LSC001 Lesch-Nyhan Syndrome 62 6.775
611
LNG031 Lung Benign Neoplasm 51 6.771
612
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 55 6.768
613
SFT003 Soft Tissue Sarcoma 57 6.763
614
P RTT002 Rett Syndrome 79 6.758
615
c THY109 Thyroid Cancer, Nonmedullary, 1 55 6.752
616
YLL002 Yellow Fever 61 6.742
617
WTH001 Withdrawal Disorder 48 6.720
618
c MCR112 Microvascular Complications of Diabetes 2 42 6.716
619
ORT008 Orotic Aciduria 57 6.711
620
DWR001 Dwarfism 44 6.694
621
LYM027 Lymphopenia 56 6.681
622
PRP080 Peripheral Artery Disease 54 6.657
623
ART016 Aortic Aneurysm 68 6.656
624
P CTN015 Cutaneous T Cell Lymphoma 48 6.641
625
LMY002 Leiomyoma 51 6.629
626
STN013 Stenotrophomonas Maltophilia Infection 26 6.624
627
CYS010 Cystinosis 62 6.617
628
JPN002 Japanese Encephalitis 61 6.609
629
DMY004 Demyelinating Disease 50 6.585
630
SPN051 Spondylitis 51 6.585
631
INF009 Inflammatory Spondylopathy 30 6.585
632
PRG017 Paraganglioma and Gastric Stromal Sarcoma 63 6.583
633
c HMC039 Hemochromatosis, Type 1 73 6.577
634
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 6.575
635
P LCH002 Lichen Planus 54 6.559
636
ARG007 Argininemia 58 6.559
637
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 6.555
638
ILS001 Ileus 50 6.551
639
CND006 Candida Glabrata 30 6.550
640
CLR030 Clear Cell Renal Cell Carcinoma 54 6.548
641
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 6.530
642
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 6.530
643
P MTR014 Motor Neuron Disease 65 6.514
644
P BRB001 Beriberi 44 6.496
645
P ICH004 Ichthyosis 56 6.492
646
DBT002 Diabetic Autonomic Neuropathy 41 6.466
647
PLM031 Poliomyelitis 63 6.456
648
c BLD140 Blood Group, I System 46 6.455
649
c 2HY001 2-Hydroxyglutaric Aciduria 38 6.446
650
P MYS005 Myositis 56 6.441
651
PLG002 Plague 58 6.433
652
HYP080 Hypogonadism 50 6.431
653
P NRC002 Narcolepsy 56 6.419
654
OVR094 Ovarian Epithelial Cancer 39 6.409
655
DBT004 Diabetic Polyneuropathy 50 6.394
656
MST004 Mast Cell Neoplasm 42 6.375
657
PLS011 Plasmacytoma 56 6.374
658
CRT015 Carotid Artery Occlusion 45 6.365
659
EXT007 Extracutaneous Mastocytoma 38 6.361
660
VRL011 Viral Infectious Disease 61 6.359
661
P PHC019 Pheochromocytoma-Paraganglioma 35 6.359
662
CHR066 Chronic Fatigue Syndrome 60 6.330
663
EXT006 Extrahepatic Cholestasis 40 6.325
664
MCR013 Microphthalmia 60 6.314
665
HND015 Hand Skill, Relative 30 6.305
666
THY125 Thyroid Gland Medullary Carcinoma 48 6.274
667
P PLY018 Polycythemia 56 6.274
668
P ASP006 Aspergillosis 72 6.273
669
P CHN012 Chondrosarcoma 57 6.267
670
CNN005 Connective Tissue Disease 67 6.260
671
P OPT006 Optic Nerve Disease 58 6.259
672
HYP025 Hyperphosphatemia 48 6.256
673
SKN019 Skin Melanoma 71 6.223
674
c GRV008 Graves Disease 1 54 6.196
675
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 6.153
676
TNS005 Tonsillitis 57 6.151
677
RTN020 Retinal Vascular Disease 46 6.148
678
ERL001 Early Myoclonic Encephalopathy 62 6.107
679
PST021 Postpartum Depression 50 6.099
680
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 6.093
681
P MYS003 Myasthenia Gravis 68 6.063
682
CHR100 Chronic Ulcer of Skin 57 6.060
683
c SPN225 Spondyloarthropathy 1 70 6.056
684
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 60 6.047
685
CRC021 Carcinosarcoma 64 6.023
686
BRT005 Barth Syndrome 56 6.009
687
KWS001 Kwashiorkor 45 6.002
688
BRN002 Bronchiolitis 57 5.995
689
ASP007 Aspiration Pneumonia 49 5.990
690
c PRM005 Primary Hyperparathyroidism 59 5.989
691
EPT021 Epithelial Recurrent Erosion Dystrophy 46 5.985
692
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 5.983
693
CHK001 Chikungunya 60 5.974
694
P VTR007 Vitreoretinopathy 46 5.967
695
HRY003 Hairy Cell Leukemia 61 5.960
696
CNV004 Canavan Disease 62 5.949
697
NRM005 Neuromuscular Disease 63 5.943
698
c GLC092 Glaucoma, Primary Open Angle 62 5.939
699
c EXD008 Exudative Vitreoretinopathy 1 71 5.936
700
FCL014 Focal Epilepsy 53 5.927
701
BTN004 Biotin Deficiency 45 5.922
702
LST001 Listeriosis 59 5.919
703
c L2H001 L-2-Hydroxyglutaric Aciduria 49 5.917
704
c SCN007 Secondary Hyperparathyroidism 51 5.894
705
PRM329 Premature Aging 36 5.868
706
LKP003 Leukoplakia 39 5.852
707
P FTL001 Fetal Alcohol Syndrome 55 5.850
708
P PGT001 Paget's Disease of Bone 61 5.843
709
INT002 Intermittent Claudication 61 5.834
710
c TBR025 Tuberous Sclerosis 1 84 5.832
711
SDD001 Sudden Infant Death Syndrome 60 5.829
712
VLV047 Volvulus of Midgut 52 5.826
713
P CNR004 Cone-Rod Dystrophy 2 74 5.823
714
NRT004 Neuritis 53 5.821
715
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 5.811
716
RST023 Resting Heart Rate, Variation in 40 5.787
717
WST001 West Syndrome 59 5.781
718
CHR178 Chromosomal Triplication 34 5.777
719
MLT157 Multiple System Atrophy 1 69 5.775
720
PTH003 Pathologic Nystagmus 52 5.774
721
OBS002 Obsessive-Compulsive Disorder 68 5.771
722
P OLG002 Oligodendroglioma 66 5.757
723
P ADL017 Adult T-Cell Leukemia 56 5.737
724
P CRV039 Cervicitis 52 5.731
725
FMR004 Fumarase Deficiency 50 5.727
726
BCT004 Bacteriuria 47 5.726
727
MTC004 Mitochondrial Encephalomyopathy 42 5.725
728
P MRC003 Mercury Poisoning 49 5.701
729
LMY003 Leiomyomatosis 44 5.685
730
INT020 Intravenous Leiomyomatosis 36 5.685
731
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 5.682
732
P INT070 Intestinal Obstruction 57 5.678
733
ALC006 Alcoholic Hepatitis 61 5.675
734
c MLT156 Multiple Endocrine Neoplasia, Type I 72 5.660
735
HRT011 Heart Septal Defect 49 5.659
736
PLR008 Pleurisy 50 5.649
737
P ATX030 Ataxia-Telangiectasia 80 5.649
738
GSG001 Gas Gangrene 52 5.645
739
MNN009 Meningoencephalitis 48 5.639
740
P DBT005 Diabetes Insipidus 54 5.637
741
CMB007 Combined Immunodeficiency 57 5.626
742
CYN002 Cyanosis, Transient Neonatal 43 5.621
743
SHG001 Shigellosis 63 5.603
744
ANP008 Anaplastic Oligoastrocytoma 29 5.600
745
P MYG005 Myoglobinuria 40 5.599
746
HMG005 Hemoglobinopathy 56 5.591
747
P NRN021 Neuronal Ceroid Lipofuscinosis 65 5.590
748
CRD223 Cardiac Arrhythmia 63 5.579
749
TRD006 Tardive Dyskinesia 53 5.577
750
P CHR071 Charcot-Marie-Tooth Disease 64 5.570
751
P TRT010 Teratoma 51 5.565
752
c TYR012 Tyrosinemia, Type I 61 5.559
753
P HML001 Hemolytic-Uremic Syndrome 52 5.554
754
ILT001 Ileitis 48 5.546
755
P SYP003 Syphilis 59 5.541
756
HPT014 Hepatorenal Syndrome 49 5.534
757
P RBL001 Rubella 58 5.526
758
TBR011 Tuberculous Meningitis 48 5.516
759
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 5.513
760
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 5.512
761
KRT001 Keratoconjunctivitis Sicca 50 5.509
762
MCL006 Macular Retinal Edema 57 5.503
763
TCK001 Tick-Borne Encephalitis 59 5.502
764
c 3MT015 3-Methylglutaconic Aciduria, Type I 51 5.502
765
P MNC007 Monocytic Leukemia 47 5.497
766
BRC012 Brucellosis 66 5.495
767
P MMP001 Mumps 57 5.494
768
P PTS002 Ptosis 52 5.492
769
INT066 Interstitial Lung Disease 60 5.476
770
MYL020 Myelomeningocele 51 5.475
771
ACT003 Acute Kidney Tubular Necrosis 46 5.474
772
SPT004 Septic Arthritis 58 5.469
773
CRB090 Cerebral Hypoxia 42 5.453
774
NRM022 Neurometabolic Disease 24 5.444
775
RTC012 Reticuloendotheliosis, X-Linked 35 5.431
776
PLC005 Placental Insufficiency 56 5.428
777
AMN001 Amenorrhea 54 5.420
778
P THY023 Thymoma 64 5.419
779
c THY107 Thymoma, Familial 42 5.415
780
P LRY019 Laryngitis 53 5.406
781
P TCD001 Tic Disorder 49 5.385
782
P RNL015 Renal Hypertension 45 5.375
783
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 5.369
785
RHM001 Rheumatic Fever 59 5.368
786
BRN056 Bronchopulmonary Dysplasia 56 5.363
787
P VNT002 Ventricular Septal Defect 58 5.359
788
P PLM034 Pulmonary Emphysema 58 5.346
789
GLY010 Glycine Encephalopathy 57 5.336
790
P HYP111 Hyperprolinemia 45 5.335
791
c CNT035 Central Nervous System Disease 54 5.317
792
ALP077 Alpha-Methylacetoacetic Aciduria 52 5.308
793
P ALP009 Alopecia Areata 59 5.299
794
LNT004 Lentigines 46 5.295
795
INT067 Interstitial Nephritis 46 5.294
796
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 5.266
797
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 5.262
798
SPP011 Suppression of Tumorigenicity 12 61 5.252
799
INT075 Intracranial Hypertension 53 5.248
800
P RRT020 Rare Tumor 39 5.239
801
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 51 5.234
802
ANP005 Anaplastic Astrocytoma 57 5.206
803
P SPR120 Supranuclear Palsy, Progressive, 1 69 5.180
804
CLL003 Cellulitis 53 5.179
805
P MTH007 Methemoglobinemia 46 5.171
806
HST006 Histidinemia 48 5.166
807
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 5.165
808
PSR001 Psoriatic Arthritis 62 5.139
809
MCR017 Macrocytic Anemia 44 5.136
810
DFF005 Diffuse Large B-Cell Lymphoma 54 5.134
811
HVY002 Heavy Metal Poisoning 22 5.133
812
CNN003 Conn's Syndrome 79 5.131
813
ATN005 Autonomic Dysfunction 46 5.119
814
PLR007 Pleural Empyema 51 5.106
815
VTM033 Vitamin K Deficiency Bleeding 48 5.101
816
PPL002 Papillary Carcinoma 46 5.094
817
OST011 Osteomalacia 52 5.088
818
URT001 Urethritis 53 5.084
819
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 5.084
820
c PRS136 Prostate Cancer, Hereditary, 6 33 5.081
821
c PRS130 Prostate Cancer, Hereditary, 8 32 5.081
822
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 5.078
823
CLL010 Cellular Ependymoma 57 5.071
824
P APL001 Aplastic Anemia 73 5.052
825
c RNG015 Ring Chromosome 2 22 5.049
826
LRN003 Learning Disability 49 5.047
827
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 5.019
828
P MLG056 Malignant Hyperthermia 66 5.009
829
P MYP006 Myopia 56 4.998
830
P FLL037 Follicular Lymphoma 74 4.993
831
P BNG030 Benign Ependymoma 51 4.991
832
FNG017 Fungal Infectious Disease 54 4.983
833
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 4.972
834
c PRX059 Peroxisome Biogenesis Disorder 1a 56 4.962
835
CTN007 Cutaneous Leishmaniasis 62 4.958
836
MLN011 Malonyl-Coa Decarboxylase Deficiency 37 4.951
837
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 4.950
838
CHL045 Choline Deficiency Disease 39 4.946
839
P MYT002 Myotonic Dystrophy 51 4.942
840
P MST009 Mastocytosis 64 4.938
841
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 4.931
842
OCL006 Ocular Hypertension 53 4.898
843
HYP043 Hyperandrogenism 48 4.892
844
INF034 Infective Endocarditis 54 4.890
845
c MCL062 Mucolipidosis Ii Alpha/beta 68 4.876
846
c NRF024 Neurofibromatosis, Type I 72 4.872
848
ENC005 Encephalomalacia 44 4.854
849
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 4.837
850
DMP001 Dumping Syndrome 43 4.828
851
SYS003 Systolic Heart Failure 49 4.811
852
P CRB088 Cerebral Atrophy 33 4.809
853
c PRG020 Paragangliomas 3 39 4.807
854
LPR001 Lepromatous Leprosy 49 4.800
855
EPL131 Epilepsy, Pyridoxine-Dependent 45 4.795
856
MSN004 Mesenchymal Cell Neoplasm 42 4.792
857
RTN003 Retinal Ischemia 49 4.775
858
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 4.774
859
TND005 Tendinitis 54 4.770
860
c ATM075 Autoimmune Encephalitis 40 4.769
861
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 4.755
862
VNH007 Von Hippel-Lindau Syndrome 73 4.749
864
BNN003 Bone Inflammation Disease 48 4.737
865
GLC086 Glucocorticoid-Induced Osteoporosis 43 4.735
866
ERY003 Erythema Multiforme 56 4.734
867
P PMP001 Pemphigus 55 4.733
868
MNT001 Mantle Cell Lymphoma 67 4.713
869
P CHL002 Childhood Absence Epilepsy 63 4.709
870
P PRP003 Porphyria Cutanea Tarda 66 4.709
871
c HRD002 Hereditary Angioedema 62 4.707
872
SLC006 Silicosis 56 4.704
873
IDP070 Idiopathic Scoliosis 42 4.700
874
CHD004 Chudley-Mccullough Syndrome 48 4.695
875
VGN019 Vaginal Discharge 47 4.691
876
ASP008 Aspiration Pneumonitis 42 4.681
877
CRY003 Cryptosporidiosis 56 4.681
878
c TYR013 Tyrosinemia, Type Ii 49 4.679
879
c DFN360 Deafness, Autosomal Dominant 69 34 4.673
880
MYC006 Mycosis Fungoides 65 4.669
881
c PRG018 Paragangliomas 1 59 4.667
882
NNT012 Neonatal Jaundice 53 4.654
883
RNL065 Renal Cell Carcinoma, Papillary, 1 79 4.653
884
HRP004 Herpes Zoster 61 4.647
885
c PRG021 Paragangliomas 4 37 4.646
886
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 4.627
887
P END047 Endophthalmitis 53 4.623
888
NRG002 Neurogenic Bladder 55 4.616
889
CHL147 Chlamydia Pneumonia 47 4.613
890
PLS007 Plasmodium Falciparum Malaria 52 4.596
891
LMB024 Limbic Encephalitis 43 4.593
892
P DRM010 Dermatomyositis 61 4.589
893
CYS005 Cysticercosis 60 4.585
894
END072 Endotheliitis 36 4.583
895
LYM009 Lymphocytic Choriomeningitis 46 4.581
896
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 4.577
897
ORL005 Oral Candidiasis 56 4.570
898
P HYP040 Hypospadias 51 4.561
899
CMB011 Combined Malonic and Methylmalonic Aciduria 42 4.561
900
ACT078 Acute Porphyria 49 4.553
901
CRD137 Cardiogenic Shock 56 4.548
902
AND005 Androgen Insensitivity Syndrome, Mild 21 4.541
903
NRN005 Neuronal Ceroid-Lipofuscinoses 61 4.537
904
c SPR086 Spermatogenic Failure 3 46 4.521
905
CCC002 Coccidiosis 50 4.519
906
P PLY041 Polymyositis 59 4.511
907
PNM008 Pneumothorax 54 4.505
908
SNS003 Sensory Peripheral Neuropathy 52 4.504
909
APH002 Aphasia 56 4.491
910
NRL005 Neurilemmoma 60 4.491
911
MLG079 Malignant Pleural Mesothelioma 42 4.490
912
PMP014 Pemphigoid 51 4.487
913
c MTC060 Mitochondrial Dna Depletion Syndrome 9 50 4.482
914
NRF007 Neurofibroma 64 4.481
915
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 4.481
916
P FCL005 Focal Segmental Glomerulosclerosis 57 4.481
917
ABT001 Abetalipoproteinemia 68 4.481
918
ATX019 Ataxia with Vitamin E Deficiency 44 4.469
919
c ACT004 Acute Diarrhea 40 4.463
920
P RNV001 Renovascular Hypertension 49 4.447
921
HST010 Histiocytosis 49 4.431
922
NWB001 Newborn Respiratory Distress Syndrome 56 4.422
923
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 4.422
924
APH001 Aphthous Stomatitis 58 4.416
925
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 4.405
926
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 4.387
927
P ALG028 Alagille Syndrome 1 73 4.384
928
GST037 Gastroparesis 52 4.384
929
P OPT009 Optic Neuritis 57 4.383
930
THR016 Thrombophlebitis 50 4.381
931
P VSC018 Visceral Steatosis 32 4.381
932
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 47 4.377
933
BTN003 Biotinidase Deficiency 62 4.376
934
P CLS010 Cluster Headache 42 4.374
935
P HYP838 Hyperlipidemia, Familial Combined, 3 61 4.369
936
P AGG001 Aggressive Periodontitis 55 4.369
937
ORL013 Oral Lichen Planus 46 4.365
938
KLB003 Klebsiella Pneumonia 50 4.361
939
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 4.353
940
PLY100 Polyploidy 36 4.350
941
HYP003 Hypermethioninemia 51 4.344
942
PYR037 Pyruvate Carboxylase Deficiency 45 4.328
943
c PRT132 Protoporphyria, Erythropoietic, 1 61 4.328
944
MST020 Mast Cell Activation Syndrome 28 4.309
945
ADR016 Adrenal Cortical Carcinoma 62 4.306
946
PCK003 Pick Disease of Brain 69 4.305
947
P GLL018 Gallbladder Cancer 53 4.305
948
RBF001 Riboflavin Deficiency 49 4.302
949
P LMY004 Leiomyosarcoma 62 4.296
950