Search results for Citric acid

1372 hits were found for Citric acid

# Family MCID Name MIFTS Score
1
LYS012 Lysosomal Acid Lipase Deficiency 64 41.095
2
NPH078 Nephrolithiasis, Uric Acid 39 35.983
3
c GLY008 Glycogen Storage Disease Ii 72 33.874
4
TRC120 Tricarboxylic Acid Cycle, Defect of 16 31.642
5
P MPL001 Maple Syrup Urine Disease 69 27.041
6
LPD008 Lipid Metabolism Disorder 61 26.906
7
RFS006 Refsum Disease, Classic 63 24.840
8
GST092 Gastroesophageal Reflux 60 23.532
9
NNL005 Non-Alcoholic Fatty Liver Disease 63 20.628
10
FTT001 Fatty Liver Disease 61 19.972
11
ISV001 Isovaleric Acidemia 54 19.850
12
ALK013 Alkaptonuria 58 19.825
13
RPD005 Rapidly Involuting Congenital Hemangioma 48 19.755
14
HYP781 Hypoascorbemia 52 19.397
15
ARG002 Argininosuccinic Aciduria 61 17.501
16
CHL068 Cholestasis 61 17.446
17
HYP014 Hyperuricemia 51 16.869
18
MTB004 Metabolic Acidosis 48 16.576
19
P LVR013 Liver Disease 68 15.980
20
GT001 Gout 63 15.872
21
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 15.738
22
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 15.607
23
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 15.603
24
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 15.602
25
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 15.602
26
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 15.602
27
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 15.602
28
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 15.602
29
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 15.602
30
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 15.602
31
LVR012 Liver Cirrhosis 62 15.135
32
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 15.099
33
c TYP009 Type 2 Diabetes Mellitus 92 14.958
34
P ACN011 Acne 55 14.915
35
ORG002 Organic Acidemia 43 14.854
36
48X005 48,xyyy 39 14.555
37
OST012 Osteoarthritis 77 14.467
38
P NRB001 Neuroblastoma 66 14.412
39
HLX001 Helix Syndrome 47 14.358
40
P PRD008 Periodontitis 64 14.196
41
P SZR006 Seizure Disorder 69 14.162
42
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 14.094
43
P HYP750 Hypertriglyceridemia, Familial 62 14.076
44
BNR002 Bone Resorption Disease 47 13.980
45
CLT003 Colitis 63 13.818
46
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 13.739
47
P BRS047 Breast Cancer 97 13.486
48
NNL006 Non-Alcoholic Steatohepatitis 54 13.435
49
HYP066 Hyperglycemia 60 13.431
50
P DBT009 Diabetes Mellitus 67 13.261
51
P CLR023 Colorectal Cancer 100 13.245
52
c CHR684 Chronic Kidney Disease 74 13.169
53
c HYP836 Hypercholesterolemia, Familial, 1 73 13.162
54
ISC004 Ischemia 61 13.114
55
DFC004 Deficiency Anemia 74 13.050
56
IRN002 Iron Metabolism Disease 56 13.021
57
GLL048 Glial Tumor 52 12.996
58
AGN016 Aging 54 12.994
59
P CRN300 Coronary Heart Disease 1 73 12.992
60
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 12.908
61
GLM045 Glioma 62 12.894
62
PRM236 Primary Biliary Cholangitis 62 12.864
63
P LKM002 Leukemia 66 12.812
64
P DDN001 Duodenal Ulcer 53 12.743
65
P KDN018 Kidney Disease 72 12.735
66
ALL029 Allergic Disease 61 12.613
67
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 12.609
68
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 12.560
69
ATH013 Atherosclerosis Susceptibility 63 12.437
70
P ESP024 Esophagitis 60 12.174
71
P OST002 Osteoporosis 77 12.057
72
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 12.057
73
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 12.057
74
c GLL024 Gallbladder Disease 1 53 12.016
75
GLB002 Glioblastoma 67 11.970
76
PPT005 Peptic Ulcer Disease 58 11.817
77
P GST044 Gastritis 55 11.802
78
RCK004 Rickets 65 11.703
79
KRT002 Keratomalacia 54 11.643
80
LPP008 Lipoprotein Quantitative Trait Locus 65 11.635
81
HMN044 Human Immunodeficiency Virus Type 1 76 11.568
82
P DRR001 Diarrhea 55 11.559
83
CYS001 Cystic Fibrosis 77 11.479
84
P HPT023 Hepatocellular Carcinoma 95 11.427
85
P ENC018 Encephalopathy 62 11.321
86
ULC004 Ulcerative Colitis 74 11.316
87
P HPT021 Hepatitis 68 11.249
88
P PRS040 Prostate Cancer 95 11.231
89
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 11.223
90
ADR007 Adrenoleukodystrophy 74 11.205
91
CRH001 Crohn's Disease 80 11.191
92
PHN003 Phenylketonuria 76 11.057
93
NPH009 Nephrolithiasis 54 10.864
94
P ART022 Arthritis 70 10.807
95
HYP266 Hypoxia 56 10.801
96
P BND020 Bone Disease 60 10.763
97
HLC007 Helicobacter Pylori Infection 67 10.646
98
P BPL003 Bipolar Disorder 56 10.638
99
P PSR002 Psoriasis 63 10.613
100
c MJR024 Major Affective Disorder 9 40 10.590
101
c MJR022 Major Affective Disorder 8 37 10.590
102
DRM006 Dermatitis 62 10.590
103
P INF037 Inflammatory Bowel Disease 53 10.568
104
P HRT032 Heart Disease 84 10.549
105
DWN001 Down Syndrome 70 10.433
106
c LKM061 Leukemia, Acute Myeloid 83 10.394
107
PRT037 Pertussis 49 10.308
108
P MYP004 Myopathy 67 10.228
109
P MYL006 Myeloid Leukemia 60 10.218
110
P ALZ034 Alzheimer Disease 87 10.197
111
P LNG032 Lung Cancer 98 10.180
112
P INF038 Influenza 68 10.166
113
P EPL164 Epilepsy 70 10.093
114
P PNC035 Pancreatic Cancer 86 10.087
115
MYL069 Myeloma, Multiple 77 10.047
116
PST011 Pustulosis of Palm and Sole 52 9.994
117
IMM167 Immune Deficiency Disease 77 9.977
118
HYP056 Hypoglycemia 65 9.950
119
c HYP595 Hypertension, Essential 84 9.945
120
P NRP001 Neuropathy 59 9.922
121
c TYP008 Type 1 Diabetes Mellitus 77 9.802
122
ALC007 Alcohol Dependence 65 9.762
123
HMC014 Homocysteinemia 52 9.760
124
MNT002 Mental Depression 56 9.732
125
CYT002 Cytokine Deficiency 43 9.717
126
HYP060 Hyperinsulinism 53 9.674
127
HRW001 Hair Whorl 35 9.662
128
DPR016 Depression 65 9.503
129
c ACT027 Acute Pancreatitis 60 9.472
130
URL001 Urolithiasis 45 9.443
131
BRN071 Brain Injury 50 9.412
132
P PNC044 Pancreatitis 61 9.383
133
END086 End Stage Renal Disease 54 9.324
134
PLM129 Pulmonary Disease, Chronic Obstructive 74 9.321
135
P DRM053 Dermatitis, Atopic 65 9.209
136
P VSC007 Vascular Disease 62 9.181
137
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 9.163
138
47X002 47,xyy 48 9.163
139
HPT019 Hepatic Encephalopathy 59 9.125
140
STR067 Stroke, Ischemic 79 9.118
141
P ADN016 Adenocarcinoma 63 9.112
142
P GST053 Gastric Cancer 82 9.055
143
BCT022 Bacterial Infectious Disease 56 9.047
144
P RHM011 Rheumatoid Arthritis 81 9.047
145
c ACT071 Acute Kidney Failure 60 9.046
146
P MYC084 Mycobacterium Tuberculosis 1 68 9.043
147
P ATS364 Autism 72 9.007
148
HPT004 Hepatic Coma 43 9.004
149
P LCT001 Lactic Acidosis 50 8.964
150
P MYC007 Myocardial Infarction 69 8.908
151
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 8.885
152
c INH020 Inherited Metabolic Disorder 47 8.852
153
PRS047 Prostatitis 58 8.852
154
c ATS007 Autism Spectrum Disorder 72 8.787
155
TRM010 Traumatic Brain Injury 50 8.786
156
P TRN020 Turner Syndrome 67 8.773
157
P HNT016 Huntington Disease 73 8.750
158
P GLM040 Glioma Susceptibility 1 70 8.696
159
GST023 Gastric Ulcer 52 8.651
160
c MCR120 Microvascular Complications of Diabetes 7 47 8.611
161
OST159 Osteogenic Sarcoma 66 8.607
162
CRB039 Cerebrovascular Disease 65 8.605
163
c ACT068 Acute Cystitis 61 8.603
164
PRT036 Peritonitis 65 8.582
165
P ALC033 Alcohol Use Disorder 67 8.573
166
c HPT001 Hepatitis C 61 8.563
167
P AST005 Asthma 76 8.545
168
P OVR042 Ovarian Cancer 88 8.529
169
ESP021 Esophageal Cancer 84 8.525
170
P MLN008 Melanoma 75 8.506
171
SKN016 Skin Disease 62 8.485
172
c MCR113 Microvascular Complications of Diabetes 3 52 8.478
173
c AMY091 Amyotrophic Lateral Sclerosis 1 88 8.472
174
c HPT003 Hepatitis a 63 8.421
175
P MJR001 Major Depressive Disorder 68 8.401
176
NPH091 Nephrolithiasis, Calcium Oxalate 61 8.396
177
P HRP006 Herpes Simplex 65 8.393
178
c HPT016 Hepatitis B 62 8.348
179
DNT012 Dental Caries 53 8.315
180
STM007 Stomatitis 52 8.304
181
c MCR133 Microvascular Complications of Diabetes 4 41 8.303
182
c MCR130 Microvascular Complications of Diabetes 6 41 8.301
183
ADN018 Adenoma 58 8.276
184
URT049 Urate Oxidase, Pseudogene 24 8.266
185
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 8.256
186
P CRD246 Cardiovascular System Disease 55 8.242
187
P URN019 Urinary Tract Infection 49 8.241
188
CHL014 Cholera 62 8.225
189
P SCH015 Schizophrenia 74 8.188
190
CRV035 Cervical Cancer 72 8.177
191
c HPT073 Hepatitis C Virus 71 8.155
192
P BCL017 B-Cell Lymphoma 57 8.151
193
SRC014 Sarcoma 64 8.147
194
P INF032 Infertility 60 8.146
195
P BLD134 Bladder Cancer 79 8.144
196
SPN035 Spindle Cell Sarcoma 51 8.140
197
P LTR001 Lateral Sclerosis 58 8.120
198
PRP001 Propionic Acidemia 65 8.095
199
c SML038 Small Cell Cancer of the Lung 69 8.089
200
URM002 Uremia 47 8.082
201
GLC003 Glucose Intolerance 53 8.067
202
PRT251 Proteinuria, Chronic Benign 58 8.046
203
ADR022 Adrenomyeloneuropathy 39 8.034
204
PRP027 Peripheral Vascular Disease 71 7.996
205
MYL009 Myelodysplastic Syndrome 67 7.990
206
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 7.903
207
HGH043 High Grade Glioma 46 7.899
208
OCL069 Ocular Motor Apraxia 57 7.894
209
KRT009 Keratosis 52 7.882
210
PPL052 Papillomatosis, Confluent and Reticulated 34 7.875
211
P THR014 Thrombocytopenia 66 7.865
212
STT001 Status Epilepticus 58 7.844
213
PPT001 Peptic Esophagitis 51 7.805
214
NTR005 Nutritional Deficiency Disease 60 7.729
215
SPN186 Spinal Cord Injury 61 7.724
216
CHL123 Chlamydia 58 7.708
217
GST033 Gestational Diabetes 61 7.703
218
CYS013 Cystinuria 66 7.682
219
c DWL002 Dowling-Degos Disease 1 58 7.676
220
c MGR028 Migraine with or Without Aura 1 64 7.622
221
VTM002 Vitamin B12 Deficiency 48 7.601
222
P MLT020 Multiple Sclerosis 79 7.569
223
CNG034 Congestive Heart Failure 69 7.567
224
INS024 Insulin-Like Growth Factor I 77 7.563
225
BRN024 Bronchitis 67 7.557
226
RNL114 Renal Cell Carcinoma, Nonpapillary 79 7.506
227
SVR001 Severe Acute Respiratory Syndrome 68 7.497
228
ANT039 Antisynthetase Syndrome 55 7.495
229
ADL002 Adult Syndrome 69 7.480
230
TXC005 Toxic Shock Syndrome 62 7.472
231
P PNM007 Pneumonia 64 7.468
232
HYP005 Hypokalemia 55 7.451
233
P ANR048 Aniridia 1 66 7.434
234
P HYP086 Hypothyroidism 69 7.426
235
P ZLL001 Zellweger Syndrome 65 7.318
236
ACQ007 Acquired Immunodeficiency Syndrome 58 7.301
237
CRD132 Cardiac Conduction Defect 59 7.284
238
GST050 Gastrointestinal System Disease 55 7.273
239
P ADL010 Adult Respiratory Distress Syndrome 71 7.236
240
P ATR011 Atrial Fibrillation 66 7.233
241
P OVR082 Overgrowth Syndrome 42 7.164
242
c DNT047 Dentinogenesis Imperfecta Type 2 35 7.144
243
SQM006 Squamous Cell Carcinoma 59 7.131
244
MLG169 Malignant Astrocytoma 57 7.131
245
c SYS001 Systemic Lupus Erythematosus 86 7.128
246
P ATT013 Attention Deficit-Hyperactivity Disorder 66 7.115
247
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 7.110
249
DBT010 Diabetic Neuropathy 54 7.089
250
P RHN004 Rhinitis 57 7.077
251
P LPS004 Lupus Erythematosus 61 7.073
252
LNG099 Lung Disease 62 7.054
253
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 7.047
254
MTH071 Methane Production 25 7.030
255
P GLY013 Glycogen Storage Disease 59 7.019
256
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 7.003
257
P PRP019 Peripheral Nervous System Disease 57 6.962
258
THR024 Thrombosis 56 6.942
259
P PRK039 Parkinsonism 55 6.933
260
c MCR115 Microvascular Complications of Diabetes 5 65 6.933
261
P CTR002 Cataract 59 6.900
262
c ATR087 Atrial Standstill 1 74 6.893
263
P MSC005 Muscular Dystrophy 66 6.873
264
HMP009 Haemophilus Influenzae 41 6.871
265
GNG013 Gingivitis 59 6.816
266
NRR001 Neuroretinitis 42 6.812
267
RTN023 Retinitis 45 6.811
268
P MSC003 Muscular Atrophy 52 6.803
269
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 6.784
270
ATM095 Autoimmune Disease 61 6.751
271
VCC001 Vaccinia 49 6.735
272
P HYP265 Hypotonia 42 6.729
273
c PCH010 Pachyonychia Congenita 3 43 6.715
274
P HDC001 Headache 56 6.715
275
MTH009 Mouth Disease 57 6.708
276
MDD011 Mood Disorder 62 6.694
277
MCS002 Mucositis 55 6.685
278
P THL005 Thalassemia 56 6.628
279
CHL004 Cholelithiasis 48 6.616
280
P ALP008 Alopecia 53 6.610
281
P SKN015 Skin Carcinoma 71 6.606
282
P HYP069 Hyperparathyroidism 62 6.589
283
DYS073 Dysphagia 53 6.569
284
PLM010 Pulmonary Edema 54 6.557
285
PLM033 Pulmonary Embolism 58 6.545
286
P LKM062 Leukemia, Acute Lymphoblastic 69 6.520
287
CLN015 Colon Adenocarcinoma 64 6.517
288
P RNL007 Renal Tubular Acidosis 52 6.516
289
P AMY004 Amyloidosis 69 6.512
290
IRR002 Irritable Bowel Syndrome 65 6.508
291
IRN001 Iron Deficiency Anemia 58 6.500
292
P ART021 Arteriosclerosis 53 6.483
293
PRX001 Peroxisomal Disease 46 6.456
294
THY029 Thyroid Carcinoma 54 6.448
295
ANX004 Anoxia 40 6.419
296
HMS001 Hemosiderosis 48 6.414
297
EMB004 Embryonal Carcinoma 55 6.412
298
P PRP029 Porphyria 60 6.408
299
P TRM003 Tremor 50 6.393
300
CNS004 Constipation 56 6.380
301
P PLY011 Polycystic Ovary Syndrome 57 6.360
302
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 6.355
303
P RSP003 Respiratory Failure 74 6.336
304
LPT014 Leptin Deficiency or Dysfunction 77 6.296
305
P LKM071 Leukemia, Chronic Lymphocytic 74 6.284
306
P MTH008 Methylmalonic Acidemia 52 6.276
307
P BRS044 Breast Adenocarcinoma 58 6.272
308
P CYS018 Cystitis 59 6.269
309
ANG054 Angina Pectoris 65 6.250
310
MLR004 Malaria 78 6.211
311
GNG003 Gingival Recession 50 6.203
312
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 6.135
313
c PRD040 Periodontitis, Chronic 52 6.117
314
P EYD002 Eye Disease 57 6.117
315
P PHC003 Pheochromocytoma 70 6.100
316
CVD001 Covid-19 58 6.097
317
P MLN007 Male Infertility 56 6.084
318
P RTN008 Retinitis Pigmentosa 79 6.068
319
P PLY014 Polycystic Kidney Disease 71 6.061
320
ADR040 Adrenal Gland Pheochromocytoma 45 6.055
321
OST062 Osteoarthritis with Mild Chondrodysplasia 47 6.026
322
CRB004 Cerebral Artery Occlusion 46 6.024
323
P GLM007 Glomerulonephritis 59 6.014
324
PRP030 Purpura 54 6.014
325
c BLD140 Blood Group, I System 47 6.013
326
ALL003 Allergic Rhinitis 66 5.982
327
CLF027 Cleft Palate, Isolated 64 5.961
328
P PRK057 Parkinson Disease, Late-Onset 79 5.960
329
P CND004 Candidiasis 57 5.923
330
P RRH023 Rare Hereditary Hemochromatosis 53 5.921
331
PNG002 Pain Agnosia 51 5.917
332
DSS032 Disease by Infectious Agent 55 5.915
333
TTN003 Tetanus 64 5.899
334
c PNS012 Paine Syndrome 60 5.892
335
P PLM037 Pulmonary Hypertension 69 5.818
336
c ACT073 Acute Leukemia 59 5.796
337
BRN028 Brain Cancer 73 5.795
338
P PRS038 Personality Disorder 65 5.770
339
PRS045 Prostatic Hypertrophy 52 5.757
340
GST045 Gastroenteritis 58 5.752
341
P DMN002 Dementia 65 5.745
342
SQM013 Squamous Cell Carcinoma, Head and Neck 75 5.732
343
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 5.716
344
P NPH012 Nephrotic Syndrome 62 5.709
345
P FBR017 Fibrosarcoma 55 5.693
346
ATX019 Ataxia with Vitamin E Deficiency 44 5.666
347
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 5.664
348
P NSP012 Nasopharyngeal Carcinoma 60 5.650
349
DPH001 Diphtheria 59 5.644
350
HMN014 Human Immunodeficiency Virus Infectious Disease 54 5.633
351
P PLM036 Pulmonary Fibrosis 65 5.625
352
PPL022 Papilloma 53 5.620
353
CRV045 Cervical Intraepithelial Neoplasia 38 5.612
354
CRV002 Cervix Uteri Carcinoma in Situ 48 5.611
355
P NTR004 Neutropenia 62 5.609
356
HNS001 Hansen's Disease 32 5.609
357
P CNJ013 Conjunctivitis 66 5.603
358
P LPR021 Leprosy 3 71 5.591
359
P CHR345 Chronic Pain 50 5.588
360
MST005 Mastitis 52 5.588
361
LYM019 Lymphosarcoma 46 5.571
362
CNT047 Contact Dermatitis 57 5.561
363
AVN001 Avian Influenza 61 5.548
364
P RCT021 Rectum Cancer 54 5.547
365
c LKM063 Leukemia, Chronic Myeloid 71 5.521
366
P HYP076 Hyperthyroidism 53 5.520
367
ENM002 Enamel Erosion 25 5.513
368
P ATR005 Atrophic Gastritis 50 5.493
369
P INS002 in Situ Carcinoma 53 5.483
370
P SYS005 Systemic Scleroderma 73 5.472
371
P OBS001 Obstructive Jaundice 49 5.448
372
ATS010 Autosomal Recessive Disease 42 5.435
373
VGN023 Vaginitis 56 5.413
374
SQM002 Squamous Cell Papilloma 45 5.399
375
P GRF003 Graft-Versus-Host Disease 71 5.387
376
P KDN017 Kidney Cancer 60 5.368
377
NWC001 Newcastle Disease 48 5.359
378
ANX010 Anxiety 70 5.338
379
INT323 Intraocular Pressure Quantitative Trait Locus 63 5.336
380
MDD018 Middle East Respiratory Syndrome 44 5.322
381
P INT068 Intestinal Disease 53 5.319
382
ALL014 Allergic Encephalomyelitis 34 5.299
383
P EXN002 Exanthem 58 5.295
384
ENT004 Enthesopathy 51 5.281
385
CMM005 Common Cold 55 5.278
386
P HYP098 Hypereosinophilic Syndrome 66 5.275
387
END040 Endogenous Depression 54 5.273
388
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 5.271
389
PSY004 Psychotic Disorder 66 5.255
390
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 5.254
391
P SPP010 Suppressor of Tumorigenicity 3 51 5.253
392
P URT039 Urticaria 57 5.253
393
MMM001 Mammary Paget's Disease 53 5.210
394
PLY150 Polykaryocytosis Inducer 29 5.198
395
P BNG032 Benign Mesothelioma 53 5.193
396
PRS021 Prostatic Adenoma 43 5.193
397
c BTT014 Beta-Thalassemia 72 5.166
398
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 5.163
399
P FNC004 Fanconi Syndrome 60 5.127
400
LNG031 Lung Benign Neoplasm 51 5.127
401
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 5.098
402
c FML021 Familial Hypercholesterolemia 71 5.067
403
P THY032 Thyroiditis 56 5.039
405
P SHR001 Short Bowel Syndrome 53 5.030
406
FML035 Familial Hyperlipidemia 55 5.024
407
PLS009 Plasma Cell Neoplasm 64 5.021
408
PRS129 Prostatic Hyperplasia, Benign 48 5.012
409
INT007 Intermediate Coronary Syndrome 53 5.005
410
P SLP006 Sleep Apnea 69 4.984
411
ENT011 Enterocolitis 55 4.975
412
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 4.961
413
OTT002 Otitis Media 71 4.960
414
MLD018 Mild Cognitive Impairment 48 4.959
415
INS001 Insulinoma 59 4.955
416
SFT003 Soft Tissue Sarcoma 57 4.953
417
MGL001 Megaloblastic Anemia 59 4.946
418
BRN004 Brain Edema 54 4.909
419
PNC129 Pancreatic Adenocarcinoma 65 4.906
420
LYM133 Lymphoma, Hodgkin, Classic 74 4.881
421
END057 Endometrial Cancer 71 4.876
422
c ACT134 Acute Liver Failure 57 4.871
423
P KLZ004 Kala-Azar 1 41 4.865
424
LSH001 Leishmaniasis 63 4.865
425
P TYR004 Tyrosinemia 49 4.845
426
ALL006 Allergic Asthma 56 4.822
427
c DLT002 Dilated Cardiomyopathy 79 4.819
428
c VRL010 Viral Hepatitis 52 4.817
429
c HYP724 Hyperlipoproteinemia, Type Iii 66 4.792
430
P SRC025 Sarcoidosis 1 70 4.781
431
c SCL052 Scleroderma, Familial Progressive 60 4.780
432
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 4.764
433
DRY001 Dry Eye Syndrome 49 4.749
434
P CNR004 Cone-Rod Dystrophy 2 75 4.748
435
P PYL005 Pyelonephritis 56 4.748
436
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 4.717
437
KRT006 Keratoconjunctivitis 53 4.706
438
ASP007 Aspiration Pneumonia 49 4.705
439
PST092 Posttransplant Acute Limbic Encephalitis 29 4.692
440
P MCR129 Microvascular Complications of Diabetes 1 68 4.682
441
MSC007 Muscle Hypertrophy 64 4.682
442
CHR100 Chronic Ulcer of Skin 57 4.667
443
P ANP001 Anaplastic Large Cell Lymphoma 61 4.666
444
P MDL005 Medulloblastoma 75 4.650
445
c FNC043 Fanconi Anemia, Complementation Group E 62 4.642
446
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 4.637
447
PLC008 Placenta Disease 49 4.637
448
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 4.611
449
MSL001 Measles 61 4.602
450
ORT008 Orotic Aciduria 56 4.588
451
FMR004 Fumarase Deficiency 52 4.583
452
AMN006 Aminoaciduria 37 4.572
453
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 4.562
454
c BRN108 Branchiootic Syndrome 1 63 4.560
455
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 4.545
456
ORL011 Oral Cancer 60 4.545
457
P BNC003 Bone Cancer 58 4.540
458
ILS001 Ileus 49 4.536
459
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 4.528
460
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 34 4.506
461
TRN015 Transient Cerebral Ischemia 62 4.503
462
SCH014 Schistosomiasis 56 4.497
463
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 4.495
464
P DYS154 Dystonia 64 4.494
465
P RTN018 Retinal Disease 53 4.489
466
P INT143 Interstitial Cystitis 59 4.478
467
ISL099 Isolated Methylmalonic Acidemia 35 4.477
468
P MJR007 Major Affective Disorder 1 42 4.474
469
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 4.452
470
KPS004 Kaposi Sarcoma 76 4.449
471
RNL077 Renal Fibrosis 46 4.425
472
FDL002 Food Allergy 47 4.425
473
PRN019 Perinatal Necrotizing Enterocolitis 60 4.410
474
SBC016 Subacute Delirium 42 4.400
475
CYS010 Cystinosis 61 4.396
476
NRT001 Neurotic Disorder 56 4.395
477
P HMP007 Hemophilia 52 4.393
478
BCT002 Bacterial Vaginosis 53 4.382
479
DYS015 Dysentery 50 4.366
480
RYS001 Reye Syndrome 49 4.364
481
TRN018 Transitional Cell Carcinoma 56 4.363
482
HRN026 Hernia, Hiatus 47 4.361
483
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.353
484
LYM143 Lymphoma, Non-Hodgkin, Familial 79 4.340
485
END072 Endotheliitis 36 4.329
486
ORL015 Oral Squamous Cell Carcinoma 43 4.324
487
P CRV039 Cervicitis 52 4.303
488
DBT084 Diabetes Mellitus, Ketosis-Prone 60 4.269
489
DBT002 Diabetic Autonomic Neuropathy 40 4.268
490
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 64 4.267
491
GST040 Gastric Adenocarcinoma 66 4.267
492
PLS011 Plasmacytoma 56 4.264
493
P MYS003 Myasthenia Gravis 68 4.259
494
CHG001 Chagas Disease 65 4.235
495
AND005 Androgen Insensitivity Syndrome, Mild 21 4.226
496
ANT024 Anthrax Disease 58 4.223
497
HDN002 Head Injury 44 4.210
498
P SJG008 Sjogren Syndrome 61 4.209
499
MSC157 Muscular Dystrophy, Duchenne Type 79 4.201
500
HYP017 Hypophosphatemia 49 4.193
501
VRL011 Viral Infectious Disease 60 4.175
502
ACT058 Active Peptic Ulcer Disease 55 4.165
503
ARG004 Argyria 26 4.160
504
P UVT001 Uveitis 57 4.159
505
BRT054 Brittle Bone Disorder 74 4.156
506
KRT001 Keratoconjunctivitis Sicca 49 4.118
507
MXD026 Mixed Glioma 45 4.117
508
RLP002 Relapsing-Remitting Multiple Sclerosis 56 4.102
509
SPS057 Spasticity 43 4.097
510
HYP555 Hypertriglyceridemia, Transient Infantile 38 4.093
511
HRY003 Hairy Cell Leukemia 61 4.079
512
ANR040 Aneurysm 60 4.047
513
PHR003 Pharyngitis 57 4.043
514
ETN001 Eating Disorder 59 4.040
515
SYN007 Synovitis 54 4.037
516
PLC002 Plica Syndrome 35 4.037
517
ALL010 Allergic Contact Dermatitis 56 4.035
518
P SLM003 Salmonellosis 54 4.032
519
GLS001 Gliosarcoma 63 4.023
520
P MTR014 Motor Neuron Disease 65 4.021
521
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 4.017
522
P PLY018 Polycythemia 56 4.014
523
PRD004 Prediabetes Syndrome 52 4.010
524
P HML002 Hemolytic Anemia 62 4.010
525
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 4.009
526
OVR094 Ovarian Epithelial Cancer 39 3.986
527
HYP141 Hyperphenylalaninemia 42 3.985
528
CHL067 Cholecystitis 59 3.980
529
PYR037 Pyruvate Carboxylase Deficiency 45 3.977
530
P MTC069 Mitochondrial Disorders 57 3.965
531
P DST107 Distal Renal Tubular Acidosis 48 3.963
532
c CHR064 Chronic Monocytic Leukemia 36 3.941
533
SKN019 Skin Melanoma 70 3.934
534
ART016 Aortic Aneurysm 69 3.929
535
CNN005 Connective Tissue Disease 66 3.926
536
DWR001 Dwarfism 45 3.918
537
FBR047 Fibromyalgia 58 3.912
538
OST017 Osteomyelitis 63 3.911
539
LKP003 Leukoplakia 39 3.909
540
DSS009 Disseminated Intravascular Coagulation 56 3.903
541
P HYP061 Hypertrophic Cardiomyopathy 69 3.898
542
P OPN001 Open-Angle Glaucoma 55 3.890
543
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.890
544
LMY002 Leiomyoma 51 3.862
545
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 3.851
546
AZS001 Azoospermia 45 3.842
547
ATN004 Autonomic Neuropathy 42 3.838
548
PLG002 Plague 58 3.838
549
PRT038 Protein-Energy Malnutrition 53 3.832
550
P MYC033 Myoclonus 46 3.830
551
INT002 Intermittent Claudication 61 3.812
552
CMB011 Combined Malonic and Methylmalonic Aciduria 43 3.810
553
BCK006 Back Pain 43 3.806
554
P OLG002 Oligodendroglioma 66 3.805
555
P THY023 Thymoma 64 3.769
556
c THY107 Thymoma, Familial 42 3.768
557
RTR008 Root Resorption 44 3.751
558
HYP025 Hyperphosphatemia 47 3.750
559
c 2HY001 2-Hydroxyglutaric Aciduria 38 3.749
560
c PRM005 Primary Hyperparathyroidism 59 3.743
561
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 3.741
562
PST028 Post-Traumatic Stress Disorder 59 3.738
563
DSS008 Disease of Mental Health 74 3.736
564
P MVM001 Movement Disease 61 3.725
565
APN008 Apnea, Obstructive Sleep 66 3.704
566
RBS001 Rabies 58 3.699
567
P INT070 Intestinal Obstruction 57 3.694
568
c DRR009 Diarrhea 6 46 3.673
569
c XNT010 Xanthinuria, Type I 52 3.662
570
MCR013 Microphthalmia 60 3.659
571
DDN006 Duodenitis 50 3.659
572
HYP080 Hypogonadism 49 3.656
573
P ALP009 Alopecia Areata 59 3.645
574
CHL013 Cholecystolithiasis 37 3.638
575
THR100 Thrombocytopenic Purpura, Autoimmune 60 3.637
576
P PLM034 Pulmonary Emphysema 58 3.633
577
PLM031 Poliomyelitis 62 3.623
578
P MCR010 Microcephaly 59 3.608
579
WTH001 Withdrawal Disorder 47 3.608
580
PST021 Postpartum Depression 50 3.605
581
PLM134 Pulmonary Fibrosis, Idiopathic 76 3.591
582
HVY002 Heavy Metal Poisoning 22 3.583
583
P BRB001 Beriberi 44 3.577
584
CRB037 Cerebral Palsy 67 3.576
585
ACR007 Acromegaly 70 3.563
586
c L2H001 L-2-Hydroxyglutaric Aciduria 49 3.554
587
c HMP029 Hemophilia a 69 3.533
588
c MCR112 Microvascular Complications of Diabetes 2 42 3.532
589
PLY001 Polycythemia Vera 69 3.531
590
ORL005 Oral Candidiasis 55 3.506
591
c EXD008 Exudative Vitreoretinopathy 1 71 3.495
592
MLT157 Multiple System Atrophy 1 69 3.494
593
c MJR006 Major Affective Disorder 5 32 3.494
594
c MJR003 Major Affective Disorder 6 32 3.494
595
P RHB003 Rhabdomyosarcoma 66 3.488
596
NPH003 Nephrocalcinosis 49 3.481
597
P FNG006 Feingold Syndrome 1 61 3.477
598
AMD002 Amed Syndrome, Digenic 37 3.471
599
HMN047 Human Cytomegalovirus Infection 59 3.470
600
SLP001 Sleeping Sickness 56 3.469
601
c HYP272 Hypercholesterolemia, Familial, 3 46 3.468
602
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 3.458
603
P LCH002 Lichen Planus 55 3.457
604
ADG002 Audiogenic Seizures 25 3.454
605
YLL002 Yellow Fever 61 3.450
606
EXC002 Exocrine Pancreatic Insufficiency 42 3.436
607
P SBS003 Substance Abuse 54 3.427
608
KWS001 Kwashiorkor 44 3.409
609
MNT001 Mantle Cell Lymphoma 65 3.408
610
ANP005 Anaplastic Astrocytoma 59 3.405
611
CHR066 Chronic Fatigue Syndrome 60 3.386
612
EPT021 Epithelial Recurrent Erosion Dystrophy 46 3.384
613
P D2H002 D-2-Hydroxyglutaric Aciduria 1 52 3.380
614
P ANG015 Angioedema 56 3.371
615
HMT002 Hematologic Cancer 61 3.365
616
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 3.363
617
P SNS001 Sensorineural Hearing Loss 59 3.358
618
VSC002 Vascular Dementia 59 3.353
619
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 3.353
620
P MYS005 Myositis 56 3.347
621
P MLG074 Malignant Mesenchymoma 40 3.343
622
IMP005 Impotence 52 3.340
623
P VNW001 Von Willebrand's Disease 64 3.338
624
c PRM038 Primary Agammaglobulinemia 47 3.333
625
c SCN007 Secondary Hyperparathyroidism 51 3.316
626
FCT001 Factor Viii Deficiency 62 3.302
627
KRT019 Keratitis, Hereditary 66 3.300
628
CRC021 Carcinosarcoma 62 3.297
629
CRN041 Carnitine-Acylcarnitine Translocase Deficiency 48 3.296
630
THR004 Thrombocytosis 52 3.287
631
HYP043 Hyperandrogenism 47 3.283
632
P SLP005 Sleep Disorder 62 3.282
633
CMP010 Complex Regional Pain Syndrome 59 3.278
634
CHR178 Chromosomal Triplication 34 3.262
635
LWC001 Low Compliance Bladder 44 3.258
636
INT066 Interstitial Lung Disease 60 3.250
637
CHL079 Children's Interstitial Lung Disease 26 3.244
638
PYR009 Pyridoxine Deficiency Anemia 35 3.231
639
c JVN010 Juvenile Rheumatoid Arthritis 66 3.229
640
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 3.227
641
URT001 Urethritis 52 3.220
642
3MT001 3-Methylcrotonyl-Coa Carboxylase Deficiency 52 3.219
643
TYP007 Typhoid Fever 63 3.200
644
c MST023 Mesothelioma, Malignant 56 3.196
645
FNG017 Fungal Infectious Disease 54 3.187
646
P PRV006 Pervasive Developmental Disorder 52 3.184
647
BTN004 Biotin Deficiency 44 3.175
648
MLN011 Malonyl-Coa Decarboxylase Deficiency 37 3.166
649
P TXP001 Toxoplasmosis 60 3.154
650
P PRM002 Primary Hyperoxaluria 65 3.135
651
VSL002 Visual Epilepsy 39 3.130
652
P LRY019 Laryngitis 53 3.128
653
KRN002 Kearns-Sayre Syndrome 63 3.124
654
LYM040 Lymphoblastic Lymphoma 53 3.118
655
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 3.113
656
CNV004 Canavan Disease 61 3.103
657
c FML001 Familial Atrial Fibrillation 65 3.088
658
c GLC092 Glaucoma, Primary Open Angle 61 3.087
659
BRN056 Bronchopulmonary Dysplasia 57 3.078
660
HYD002 Hydronephrosis 58 3.071
661
APP008 Appendicitis 62 3.070
662
c SPR086 Spermatogenic Failure 3 47 3.068
663
ATN005 Autonomic Dysfunction 45 3.062
664
P OPT006 Optic Nerve Disease 57 3.032
665
c GRV008 Graves Disease 1 54 3.031
666
P VSC018 Visceral Steatosis 32 3.021
667
c THY109 Thyroid Cancer, Nonmedullary, 1 55 3.019
668
NWB001 Newborn Respiratory Distress Syndrome 56 3.013
669
P NRC002 Narcolepsy 55 3.010
670
MYL031 Myeloproliferative Neoplasm 66 3.006
671
HND015 Hand Skill, Relative 29 2.997
672
SPP011 Suppression of Tumorigenicity 12 61 2.987
673
FSC004 Fasciitis 49 2.985
674
TTH007 Tooth Erosion 29 2.982
675
APH001 Aphthous Stomatitis 57 2.982
676
LRY018 Laryngeal Squamous Cell Carcinoma 47 2.979
677
c MJR008 Major Affective Disorder 2 34 2.978
678
BRN009 Burning Mouth Syndrome 51 2.974
679
MYL005 Myelofibrosis 70 2.974
680
THY111 Thyroid Carcinoma, Familial Medullary 67 2.972
681
P CRP001 Carpal Tunnel Syndrome 66 2.966
682
INT067 Interstitial Nephritis 47 2.961
683
PPL001 Papillary Adenoma 44 2.952
684
MCR004 Macroglobulinemia 48 2.951
685
ORL012 Oral Leukoplakia 35 2.949
686
c MJR004 Major Affective Disorder 4 28 2.938
687
c MJR023 Major Affective Disorder 7 33 2.938
688
P GRV001 Graves' Disease 54 2.937
689
P HYP769 Hyperlysinemia, Type I 43 2.923
690
P RTT002 Rett Syndrome 79 2.918
691
P DBT005 Diabetes Insipidus 54 2.898
692
MYF001 Myofibroma 42 2.895
693
BRS099 Breast Ductal Carcinoma 61 2.890
694
TRY001 Trypanosomiasis 50 2.888
695
P EST001 Estrogen-Receptor Positive Breast Cancer 49 2.883
696
WST001 West Syndrome 64 2.874
697
FRZ001 Frozen Shoulder 54 2.868
698
CLR030 Clear Cell Renal Cell Carcinoma 54 2.868
699
CHR682 Chronic Bilirubin Encephalopathy 37 2.867
700
THY122 Thyroid Gland Cancer 59 2.866
701
BRN002 Bronchiolitis 57 2.853
702
MCL006 Macular Retinal Edema 56 2.849
703
P THR015 Thrombophilia 51 2.845
704
ANK001 Ankylosis 51 2.843
705
GST071 Gastrointestinal Carcinoma 46 2.841
706
P LRY044 Larynx Cancer 53 2.833
707
P MYP006 Myopia 55 2.833
708
CRY008 Cryopyrin-Associated Periodic Syndrome 48 2.832
709
PRN071 Parenteral Nutrition-Associated Cholestasis 23 2.830
710
SDD001 Sudden Infant Death Syndrome 60 2.826
711
CTS005 Catastrophic Antiphospholipid Syndrome 43 2.825
712
P ANT006 Antiphospholipid Syndrome 55 2.820
713
CNT033 Central Nervous System Cancer 47 2.813
714
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 2.806
715
P ESP035 Esophagitis, Eosinophilic, 1 57 2.799
716
HRT012 Heart Valve Disease 53 2.797
718
RFR010 Refractory Anemia 49 2.794
719
c MCL062 Mucolipidosis Ii Alpha/beta 69 2.790
720
PSR001 Psoriatic Arthritis 61 2.789
721
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 2.780
722
c ALP101 Alpha-Thalassemia 62 2.773
723
RTN020 Retinal Vascular Disease 45 2.762
724
BRS064 Bursitis 51 2.760
725
c OVR114 Ovarian Cancer 1 60 2.759
726
CRT015 Carotid Artery Occlusion 45 2.757
727
P SYP003 Syphilis 59 2.755
728
P LNG028 Long Qt Syndrome 63 2.753
729
P NJM001 Nijmegen Breakage Syndrome 75 2.744
730
HRT011 Heart Septal Defect 49 2.742
731
c PNC108 Pancreatitis, Hereditary 68 2.733
732
P ASP006 Aspergillosis 71 2.725
733
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 2.719
734
BCT004 Bacteriuria 48 2.717
735
P VNT002 Ventricular Septal Defect 58 2.702
736
LMY014 Leiomyoma, Uterine 55 2.691
737
NSP002 Nasopharyngitis 45 2.681
738
P CHR285 Chronic Myelomonocytic Leukemia 59 2.681
739
c PSR023 Psoriasis 1 52 2.677
740
ECT026 Ectopic Pregnancy 47 2.665
741
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 2.663
742
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 2.660
743
CRD223 Cardiac Arrhythmia 63 2.654
744
P MTC133 Mitochondrial Myopathy 51 2.653
745
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 2.653
746
RSP019 Respiratory Distress Syndrome in Premature Infants 52 2.639
747
BLD051 Blood Coagulation Disease 53 2.636
748
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 2.634
749
CCN002 Cocaine Abuse 49 2.631
750
c PSR017 Psoriasis 2 53 2.630
751
ACT011 Acute Contagious Conjunctivitis 42 2.629
752
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.627
753
MTC005 Mitochondrial Metabolism Disease 45 2.620
754
NRM005 Neuromuscular Disease 63 2.613
755
GLS018 Glass Syndrome 60 2.610
756
c PSR028 Psoriasis 7 43 2.607
757
c INF145 Infantile Liver Failure Syndrome 1 44 2.607
758
ACT003 Acute Kidney Tubular Necrosis 46 2.597
759
DCB001 Decubitus Ulcer 61 2.584
760
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 2.583
761
KWS002 Kawasaki Disease 65 2.581
762
GST037 Gastroparesis 52 2.580
763
BRN032 Brain Glioma 45 2.578
764
HMN048 Human Papillomavirus Infectious Disease 46 2.577
765
P PTS002 Ptosis 52 2.573
766
DRM011 Dermatophytosis 52 2.566
767
INC002 Inclusion Body Myositis 57 2.564
768
P NRV006 Nervous System Cancer 47 2.563
769
P HYP838 Hyperlipidemia, Familial Combined, 3 61 2.563
770
P RNV001 Renovascular Hypertension 49 2.558
771
P BRN022 Bronchiectasis 59 2.554
772
c PSR032 Psoriasis 11 47 2.550
773
c PSR018 Psoriasis 13 40 2.550
774
APL002 Aplasia of Lacrimal and Salivary Glands 56 2.550
775
LPT006 Leptin Receptor Deficiency 50 2.544
776
SCT005 Scott Syndrome 51 2.539
777
P GLL022 Guillain-Barre Syndrome 59 2.532
778
SRC027 Sarcoma, Synovial 58 2.521
779
HRN029 Hearing Loss, Noise-Induced 37 2.521
780
c ART101 Aortic Valve Disease 2 65 2.517
781
LST001 Listeriosis 59 2.510
782
P CTR177 Citrullinemia, Type Ii, Adult-Onset 55 2.509
783
BRC012 Brucellosis 66 2.504
784
PRM003 Premature Ejaculation 44 2.504
785
P DRM010 Dermatomyositis 61 2.501
786
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 2.498
787
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.497
788
OVR063 Overnutrition 42 2.492
789
CRB009 Cerebritis 43 2.491
790
PRT058 Pure Autonomic Failure 58 2.484
791
THY125 Thyroid Gland Medullary Carcinoma 48 2.482
792
P RBL001 Rubella 58 2.481
793
P HYP040 Hypospadias 51 2.475
794
GRW007 Growth Hormone Deficiency 47 2.466
795
P HYP726 Hypercalcemia, Infantile, 1 58 2.466
796
GST019 Gastrointestinal Stromal Tumor 78 2.462
797
OLG001 Oligospermia 45 2.460
798
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 2.457
799
PLS007 Plasmodium Falciparum Malaria 52 2.457
800
RNL065 Renal Cell Carcinoma, Papillary, 1 79 2.451
801
MCN017 Meconium Ileus 52 2.449
802
ANG005 Anogenital Venereal Wart 55 2.444
803
FRN006 Frontotemporal Dementia 68 2.439
804
DMP001 Dumping Syndrome 43 2.439
805
P FCL005 Focal Segmental Glomerulosclerosis 57 2.432
806
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 2.420
807
c DPH024 Diaphragmatic Hernia, Congenital 64 2.414
808
IDP073 Idiopathic Hypercalciuria 40 2.413
809
MYC005 Myocardial Stunning 45 2.413
810
ADN011 Adenoid Cystic Carcinoma 68 2.407
811
RST023 Resting Heart Rate, Variation in 40 2.401
812
c SYS043 Systemic Lupus Erythematosus 1 38 2.398
813
CHP002 Chops Syndrome 47 2.393
814
DCT002 Ductal Carcinoma in Situ 58 2.391
815
ASP004 Asphyxia Neonatorum 50 2.376
816
P CHR012 Chronic Granulomatous Disease 69 2.376
817
c PRM108 Primary Progressive Multiple Sclerosis 51 2.374
818
SWL001 Swallowing Disorders 38 2.365
819
c PRG106 Progressive Muscular Dystrophy 31 2.357
820
FNC002 Functional Diarrhea 39 2.357
821
JVN004 Juvenile Myelomonocytic Leukemia 67 2.355
822
CLN019 Colonic Disease 47 2.353
823
DVR002 Diverticulitis 46 2.347
824
ALL009 Allergic Conjunctivitis 51 2.342
825
CRN027 Corneal Neovascularization 47 2.330
826
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 2.321
827
BLD131 Bladder Urothelial Carcinoma 59 2.319
828
LMB062 Limb Ischemia 55 2.313
829
TBC004 Tobacco Addiction 63 2.312
830
c ACT004 Acute Diarrhea 40 2.306
831
VLV011 Vulvovaginal Candidiasis 49 2.297
832
HML018 Homologous Wasting Disease 21 2.295
833
c CHR708 Chronic Urticaria 42 2.295
834
AND014 Androgenic Alopecia 46 2.292
835
ACR041 Acromelic Frontonasal Dysostosis 53 2.286
836
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 2.285
837
P HMN032 Human Herpesvirus 8 47 2.284
838
GLT007 Glutathione Synthetase Deficiency 48 2.271
839
HMP005 Hemiplegia 53 2.263
840
P KRT007 Keratoconus 50 2.262
841
P OST135 Osteogenesis Imperfecta, Type I 60 2.257
842
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 2.249
843
P ESS003 Essential Thrombocythemia 68 2.244
844
LTN004 Late-Onset Retinal Degeneration 60 2.244
845
P MLN069 Melanoma, Uveal 59 2.235
846
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 2.231
847
P CRN024 Corneal Disease 43 2.227
848
P SML001 Small Cell Carcinoma 52 2.219
849
P GLC113 Galactosemia I 65 2.217
850
GST049 Gastrointestinal System Cancer 49 2.210
851
RYN005 Raynaud Phenomenon 45 2.209
852
DFF003 Diffuse Scleroderma 41 2.206
853
c HMN021 Human T-Cell Leukemia Virus Type 1 46 2.202
854
IRD001 Iridocyclitis 54 2.201
855
P HRD086 Hereditary Hypophosphatemic Rickets 40 2.199
856
P HMR005 Hemorrhoid 49 2.198
857
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 2.198
858
P DNT007 Dentin Sensitivity 34 2.196
859
LGH007 Leigh Syndrome 70 2.194
860
CRB090 Cerebral Hypoxia 42 2.194
861
EXT034 Extrinsic Allergic Alveolitis 56 2.191
862
P TTR001 Tetralogy of Fallot 69 2.191
863
EXR010 Exercise-Induced Bronchoconstriction 34 2.190
864
P LYM033 Lymphoproliferative Syndrome 59 2.190
865
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.188
866
PPL002 Papillary Carcinoma 46 2.186
867
c CHR417 Chronic Graft Versus Host Disease 55 2.183
868
PRM329 Premature Aging 36 2.182
869
SNS003 Sensory Peripheral Neuropathy 51 2.176
870
CMR002 Coumarin Resistance 60 2.166
871
GLN010 Glanzmann Thrombasthenia 66 2.160
872
P PRG092 Pregnancy Loss, Recurrent 1 42 2.158
873
GSG001 Gas Gangrene 52 2.155
874
PRM020 Premenstrual Tension 39 2.153
875
LNG015 Lingual-Facial-Buccal Dyskinesia 47 2.152
876
TRP004 Tropical Sprue 39 2.146
877
IRR003 Irritant Dermatitis 47 2.144
878
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 2.141
879
TST014 Testicular Cancer 51 2.141
880
OLG022 Oligoasthenoteratozoospermia 35 2.138
881
P HMN038 Human Coronavirus Sensitivity 30 2.137
882
ENT007 Enteropathica 24 2.136
883
P TRC031 Trichorhinophalangeal Syndrome 37 2.134
884
P ACT105 Acute Mountain Sickness 52 2.130
885
ALG001 Algoneurodystrophy 37 2.120
886
CMB040 Combined D-2- and L-2-Hydroxyglutaric Aciduria 40 2.113
887
P PLV020 Pelvic Organ Prolapse 58 2.111
888
STM006 Stomach Disease 47 2.102
889
KLB003 Klebsiella Pneumonia 49 2.097
890
P HML001 Hemolytic-Uremic Syndrome 52 2.094
891
SXL003 Sexual Disorder 49 2.094
892
c HRD202 Hereditary Lymphedema I 55 2.093
893
RFL001 Reflex Sympathetic Dystrophy 51 2.092
894
MNC019 Monocarboxylate Transporter 1 Deficiency 46 2.090
895
PLY100 Polyploidy 36 2.082
896
P ALP061 Alopecia, Androgenetic, 1 49 2.082
897
FLR002 Filariasis 55 2.077
898
BNM001 Bone Marrow Cancer 45 2.076
899
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 2.071
900
OST011 Osteomalacia 52 2.070
901
ACN002 Acanthosis Nigricans 56 2.063
902
c ALM001 Al Amyloidosis 54 2.060
903
P LCT002 Lactose Intolerance 52 2.058
904
ADR016 Adrenal Cortical Carcinoma 61 2.058
905
c MCL046 Mucolipidosis Iii Alpha/beta 61 2.053
906
P HYP024 Hypoparathyroidism 55 2.045
907
P TMR010 Tumor Predisposition Syndrome 69 2.044
908
MST024 Mastocytosis, Cutaneous 66 2.038
909
THR035 Thrombasthenia 48 2.036
910
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 2.033
911
PRN029 Parainfluenza Virus Type 3 32 2.029
912
P MMB011 Membranous Nephropathy 50 2.025
913
c LKM056 Leukemia, Chronic Lymphocytic 2 47 2.024
914
ORL013 Oral Lichen Planus 45 2.023
915
P PLY041 Polymyositis 59 2.022
916
MCR011 Microinvasive Gastric Cancer 41 2.015
917
CRY003 Cryptosporidiosis 55 2.014
918
P MGR003 Migraine with Aura 51 2.012
919
RSP007 Respiratory Distress Syndrome, Infant 40 2.012
920
HSH003 Hashimoto Thyroiditis 60 2.006
921
TRC003 Trichomoniasis 53 2.005
922
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 38 2.000
923
OLG003 Oligohydramnios 51 1.996
924
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.994
925
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 1.991
926
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 1.978
927
INH023 Inherited Cancer-Predisposing Syndrome 53 1.978
928
P LTH003 Lethal Congenital Contracture Syndrome 40 1.976
929
EPD015 Epidemic Typhus 44 1.973
930
SHL001 Shoulder Impingement Syndrome 35 1.972
931
RFR007 Refractory Anemia with Excess Blasts in Transformation 26 1.970
932
CRD137 Cardiogenic Shock 56 1.966
933
PRQ002 Paraquat Poisoning 28 1.965
934
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.962
935
LGN006 Legionnaire Disease 52 1.962
936
HNT002 Hantavirus Pulmonary Syndrome 55 1.955
937
LYM012 Lymphoplasmacytic Lymphoma 50 1.954
938
ACR008 Acrocallosal Syndrome 70 1.954
939
WLD007 Waldenstroem's Macroglobulinemia 65 1.950
940
EPC002 Epicondylitis 43 1.948
941
c RTN047 Retinitis Pigmentosa 18 45 1.946
942
INV001 Invasive Aspergillosis 48 1.946
943
MNN028 Mononeuropathy of the Median Nerve, Mild 46 1.944
944
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 1.935
945
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 52 1.929
946
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.929
947
RSP021 Respiratory Allergy 41 1.926
948
P PRG013