Search results for Hydrogen Ion

2139 hits were found for Hydrogen Ion

# Family MCID Name MIFTS Score
1
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 70.999
2
RPD005 Rapidly Involuting Congenital Hemangioma 46 43.716
3
HLX001 Helix Syndrome 48 42.659
4
HRW001 Hair Whorl 35 37.654
5
P NRB001 Neuroblastoma 66 21.804
6
MTB004 Metabolic Acidosis 48 20.984
7
ISC004 Ischemia 61 20.157
8
CYS001 Cystic Fibrosis 78 20.125
9
HYP266 Hypoxia 57 18.818
10
P OVR082 Overgrowth Syndrome 49 18.246
11
MTH071 Methane Production 25 18.241
12
48X005 48,xyyy 39 18.051
13
ANX004 Anoxia 40 17.291
14
c DNT047 Dentinogenesis Imperfecta Type 2 35 17.081
15
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 16.406
16
AGN016 Aging 54 15.690
17
GLL048 Glial Tumor 52 15.589
18
GLM045 Glioma 63 15.589
19
IRR002 Irritable Bowel Syndrome 65 15.271
20
P LTR001 Lateral Sclerosis 58 15.072
21
c AMY091 Amyotrophic Lateral Sclerosis 1 88 14.986
22
P ALZ034 Alzheimer Disease 87 14.696
23
GLB002 Glioblastoma 67 14.058
24
ALL029 Allergic Disease 59 14.036
25
SVR001 Severe Acute Respiratory Syndrome 67 13.932
26
P PHC003 Pheochromocytoma 69 13.836
27
ADR040 Adrenal Gland Pheochromocytoma 46 13.836
28
CHL014 Cholera 62 13.790
29
P DRR001 Diarrhea 55 13.623
30
HYP066 Hyperglycemia 61 13.385
31
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 13.259
32
PRT037 Pertussis 65 13.243
33
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 13.197
34
LNG099 Lung Disease 62 13.135
35
P LNG028 Long Qt Syndrome 64 13.119
36
47X002 47,xyy 48 12.769
37
DNT012 Dental Caries 53 12.730
38
P PRD008 Periodontitis 64 12.714
39
OST159 Osteogenic Sarcoma 66 12.582
40
c HYP595 Hypertension, Essential 85 12.573
41
c PLM127 Pulmonary Hypertension, Primary, 3 34 12.410
42
BNR002 Bone Resorption Disease 47 12.140
43
PPL052 Papillomatosis, Confluent and Reticulated 34 12.131
44
P PNC035 Pancreatic Cancer 86 12.060
45
CLT003 Colitis 63 12.022
46
BRN071 Brain Injury 50 11.913
47
P ANP001 Anaplastic Large Cell Lymphoma 61 11.832
48
BCT022 Bacterial Infectious Disease 56 11.780
49
HMN044 Human Immunodeficiency Virus Type 1 78 11.772
50
P CRD119 Cardiac Arrest 67 11.592
51
PLM129 Pulmonary Disease, Chronic Obstructive 74 11.477
52
c ACT027 Acute Pancreatitis 60 11.468
53
c CHR684 Chronic Kidney Disease 69 11.434
54
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 11.359
55
BRN004 Brain Edema 54 11.336
56
P LNG032 Lung Cancer 98 11.208
57
CRB004 Cerebral Artery Occlusion 45 11.173
58
P INF038 Influenza 68 11.126
59
TRM010 Traumatic Brain Injury 51 10.954
60
PST092 Posttransplant Acute Limbic Encephalitis 28 10.921
61
CNS004 Constipation 56 10.814
62
P ENC018 Encephalopathy 62 10.806
63
P PLM037 Pulmonary Hypertension 72 10.778
64
P PNC044 Pancreatitis 61 10.730
65
P RNL007 Renal Tubular Acidosis 50 10.727
66
P MLN008 Melanoma 76 10.674
67
SPN186 Spinal Cord Injury 61 10.654
68
MDD018 Middle East Respiratory Syndrome 44 10.633
69
HYP005 Hypokalemia 55 10.574
70
ULC004 Ulcerative Colitis 74 10.523
72
IRN002 Iron Metabolism Disease 57 10.434
73
CRD132 Cardiac Conduction Defect 60 10.425
74
CYT002 Cytokine Deficiency 43 10.387
75
PLM010 Pulmonary Edema 55 10.379
76
NPH009 Nephrolithiasis 54 10.362
77
OCL069 Ocular Motor Apraxia 57 10.350
78
c MGR028 Migraine with or Without Aura 1 64 10.320
79
P CHR345 Chronic Pain 50 10.304
80
FTT001 Fatty Liver Disease 62 10.227
81
CRD223 Cardiac Arrhythmia 63 10.078
82
DWN001 Down Syndrome 70 10.077
83
P BRS047 Breast Cancer 98 9.989
84
P NRP001 Neuropathy 60 9.983
85
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 9.891
86
P PRK057 Parkinson Disease, Late-Onset 80 9.847
87
P KDN018 Kidney Disease 72 9.814
88
P LCT002 Lactose Intolerance 52 9.795
89
P PRS040 Prostate Cancer 95 9.763
90
P GST044 Gastritis 55 9.704
91
P HPT023 Hepatocellular Carcinoma 96 9.694
92
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 9.694
93
TXC005 Toxic Shock Syndrome 62 9.686
94
P VSC007 Vascular Disease 63 9.670
95
c PRC016 Pre-Eclampsia 65 9.554
96
c HPT073 Hepatitis C Virus 71 9.520
97
ATH013 Atherosclerosis Susceptibility 63 9.484
98
HND015 Hand Skill, Relative 30 9.470
99
P CTR002 Cataract 60 9.450
100
P MYC084 Mycobacterium Tuberculosis 1 68 9.444
101
HMS001 Hemosiderosis 48 9.429
102
SKN016 Skin Disease 63 9.420
103
P HRT032 Heart Disease 81 9.385
104
P RRH023 Rare Hereditary Hemochromatosis 54 9.377
105
P ADN016 Adenocarcinoma 63 9.286
106
P AMY004 Amyloidosis 70 9.245
107
NNL005 Non-Alcoholic Fatty Liver Disease 63 9.205
108
P PRN023 Prion Disease 60 9.189
109
GNG013 Gingivitis 59 9.115
110
P EPL164 Epilepsy 68 9.110
111
HMC014 Homocysteinemia 52 9.028
112
P PRK039 Parkinsonism 55 9.017
113
P HNT016 Huntington Disease 73 9.010
114
P GLM040 Glioma Susceptibility 1 71 8.999
115
CNG034 Congestive Heart Failure 69 8.987
116
P SZR006 Seizure Disorder 70 8.847
117
c MCR130 Microvascular Complications of Diabetes 6 41 8.821
118
c MCR120 Microvascular Complications of Diabetes 7 47 8.821
119
c MCR113 Microvascular Complications of Diabetes 3 52 8.821
120
c MCR133 Microvascular Complications of Diabetes 4 41 8.821
121
c ATR087 Atrial Standstill 1 74 8.801
122
P CLR023 Colorectal Cancer 100 8.794
123
P AST005 Asthma 76 8.782
124
c SML038 Small Cell Cancer of the Lung 69 8.754
125
P BCL017 B-Cell Lymphoma 59 8.729
126
c HPT001 Hepatitis C 62 8.700
127
P MYC007 Myocardial Infarction 70 8.698
128
PLY150 Polykaryocytosis Inducer 29 8.693
129
IMP005 Impotence 52 8.664
130
P INF037 Inflammatory Bowel Disease 53 8.641
131
ALC007 Alcohol Dependence 66 8.608
132
ANT024 Anthrax Disease 58 8.592
133
P MSC005 Muscular Dystrophy 67 8.572
134
BRN024 Bronchitis 67 8.539
135
P LNG064 Lung Cancer Susceptibility 3 70 8.493
136
CHR072 Chordoma 57 8.461
137
P ADL010 Adult Respiratory Distress Syndrome 71 8.458
138
c TYP009 Type 2 Diabetes Mellitus 92 8.421
139
OST012 Osteoarthritis 77 8.415
140
P BPL003 Bipolar Disorder 56 8.394
141
P BND020 Bone Disease 59 8.382
142
c MJR022 Major Affective Disorder 8 38 8.283
143
c MJR024 Major Affective Disorder 9 41 8.283
144
c ACT071 Acute Kidney Failure 60 8.210
145
P ATR011 Atrial Fibrillation 66 8.201
146
P INF032 Infertility 57 8.189
147
DPH001 Diphtheria 59 8.186
148
P CRN300 Coronary Heart Disease 1 73 8.173
149
P PLM036 Pulmonary Fibrosis 66 8.170
150
P LVR013 Liver Disease 69 8.161
151
MCS002 Mucositis 56 8.078
152
c HYP836 Hypercholesterolemia, Familial, 1 73 8.044
153
SQM006 Squamous Cell Carcinoma 60 8.010
154
P DDN001 Duodenal Ulcer 53 7.921
155
P RSP003 Respiratory Failure 74 7.900
156
PPT005 Peptic Ulcer Disease 58 7.869
157
P PRD021 Periodic Paralysis 41 7.827
158
END086 End Stage Renal Disease 52 7.788
159
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 7.774
161
P ACN011 Acne 57 7.768
162
HMP009 Haemophilus Influenzae 41 7.767
163
P MYP004 Myopathy 67 7.751
164
P LCT001 Lactic Acidosis 51 7.737
165
CVD001 Covid-19 57 7.726
166
P RCT021 Rectum Cancer 54 7.722
167
P HRP006 Herpes Simplex 65 7.720
168
c MCR115 Microvascular Complications of Diabetes 5 65 7.711
169
P HYP086 Hypothyroidism 69 7.673
170
P CHR012 Chronic Granulomatous Disease 69 7.669
171
HGH043 High Grade Glioma 45 7.638
172
PRT251 Proteinuria, Chronic Benign 57 7.588
173
P PLY014 Polycystic Kidney Disease 69 7.558
174
P PRP019 Peripheral Nervous System Disease 58 7.558
175
P SKN015 Skin Carcinoma 71 7.529
176
URL001 Urolithiasis 46 7.489
177
c PCH010 Pachyonychia Congenita 3 43 7.488
178
c BRN108 Branchiootic Syndrome 1 62 7.475
179
DRM006 Dermatitis 62 7.422
180
CNT047 Contact Dermatitis 57 7.389
181
P MLN007 Male Infertility 56 7.355
182
ESP021 Esophageal Cancer 83 7.335
183
URM002 Uremia 47 7.310
184
LVR012 Liver Cirrhosis 63 7.295
185
SPN035 Spindle Cell Sarcoma 54 7.289
186
SRC014 Sarcoma 65 7.289
187
P FBR017 Fibrosarcoma 56 7.287
188
P RHN004 Rhinitis 57 7.271
189
GT001 Gout 64 7.260
190
P OPT006 Optic Nerve Disease 58 7.244
191
ART140 Arteries, Anomalies of 53 7.195
192
TTN003 Tetanus 65 7.114
193
P DRM053 Dermatitis, Atopic 65 7.102
194
NPH091 Nephrolithiasis, Calcium Oxalate 61 7.054
195
P DST107 Distal Renal Tubular Acidosis 48 7.012
196
ADN011 Adenoid Cystic Carcinoma 68 6.996
197
OST003 Osteonecrosis 61 6.986
198
P ART022 Arthritis 71 6.984
199
P HPT021 Hepatitis 69 6.975
200
DSS032 Disease by Infectious Agent 55 6.959
201
P HYP069 Hyperparathyroidism 62 6.951
202
LPD008 Lipid Metabolism Disorder 62 6.922
203
TLN003 Telangiectasis 51 6.905
204
P DBT009 Diabetes Mellitus 67 6.893
205
c HPT015 Hepatitis D 49 6.887
206
P NSP012 Nasopharyngeal Carcinoma 61 6.882
207
HVY002 Heavy Metal Poisoning 22 6.868
208
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 6.863
209
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 6.863
210
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 6.863
211
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 6.863
212
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 6.863
213
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 6.863
214
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 6.863
215
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 6.863
216
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 6.863
217
IMM167 Immune Deficiency Disease 78 6.863
218
URT049 Urate Oxidase, Pseudogene 24 6.850
219
ATM095 Autoimmune Disease 61 6.849
220
P ATX030 Ataxia-Telangiectasia 80 6.822
221
c DLT002 Dilated Cardiomyopathy 78 6.802
222
GST045 Gastroenteritis 58 6.771
223
MLR004 Malaria 80 6.769
224
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 6.766
225
GST023 Gastric Ulcer 52 6.759
226
MLG169 Malignant Astrocytoma 57 6.753
227
DFC004 Deficiency Anemia 74 6.747
228
P GLM007 Glomerulonephritis 60 6.722
229
CRB039 Cerebrovascular Disease 66 6.719
230
VCC001 Vaccinia 47 6.712
231
SCR011 Scrapie 39 6.692
232
PNG002 Pain Agnosia 51 6.667
233
ARG004 Argyria 26 6.660
234
STR067 Stroke, Ischemic 80 6.630
235
P ALC033 Alcohol Use Disorder 61 6.610
236
c ACT068 Acute Cystitis 61 6.591
237
HYP056 Hypoglycemia 65 6.589
238
P GST053 Gastric Cancer 83 6.588
239
P RTN016 Retinal Degeneration 52 6.559
240
INS024 Insulin-Like Growth Factor I 78 6.536
241
P KLZ004 Kala-Azar 1 41 6.520
242
LSH001 Leishmaniasis 64 6.520
243
P MYC008 Myocarditis 59 6.508
244
c LKM061 Leukemia, Acute Myeloid 83 6.493
245
PRT036 Peritonitis 65 6.478
246
SYN036 Syncope 45 6.465
247
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 6.454
248
BCT002 Bacterial Vaginosis 53 6.450
249
INS001 Insulinoma 59 6.440
250
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 6.423
251
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 6.423
252
P BRS044 Breast Adenocarcinoma 58 6.414
253
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 6.395
254
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 6.395
255
P HML002 Hemolytic Anemia 62 6.379
256
P CLC063 Celiac Disease 1 66 6.378
257
P OST002 Osteoporosis 76 6.360
258
P TRC031 Trichorhinophalangeal Syndrome 38 6.357
259
KRT019 Keratitis, Hereditary 66 6.342
260
HYP014 Hyperuricemia 51 6.342
261
CRH001 Crohn's Disease 80 6.337
262
P HYP076 Hyperthyroidism 53 6.337
263
ALL003 Allergic Rhinitis 67 6.336
264
P MRC003 Mercury Poisoning 49 6.313
265
P CHN012 Chondrosarcoma 57 6.312
266
c GLL024 Gallbladder Disease 1 52 6.295
267
MYT011 Myotonia 39 6.284
268
CLN015 Colon Adenocarcinoma 65 6.281
269
P URN019 Urinary Tract Infection 49 6.274
270
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 6.245
271
MST005 Mastitis 53 6.238
272
LPP008 Lipoprotein Quantitative Trait Locus 65 6.229
273
P MJR001 Major Depressive Disorder 68 6.216
274
GST092 Gastroesophageal Reflux 61 6.211
275
CHR100 Chronic Ulcer of Skin 57 6.209
276
P BLD134 Bladder Cancer 79 6.185
277
STN013 Stenotrophomonas Maltophilia Infection 26 6.138
278
RCK004 Rickets 68 6.134
279
NNL006 Non-Alcoholic Steatohepatitis 54 6.132
280
GST050 Gastrointestinal System Disease 55 6.126
281
c ACT075 Acute Myocardial Infarction 56 6.122
282
ACT098 Acute Erythroid Leukemia 55 6.104
283
MSC157 Muscular Dystrophy, Duchenne Type 79 6.077
284
c PRD040 Periodontitis, Chronic 52 6.071
285
P MLG056 Malignant Hyperthermia 66 6.066
286
HPT004 Hepatic Coma 43 6.059
287
P FBR031 Febrile Seizures 52 6.034
288
c TYP008 Type 1 Diabetes Mellitus 70 6.033
289
P CYS018 Cystitis 59 6.033
290
STM007 Stomatitis 54 6.028
291
P CND004 Candidiasis 58 6.025
292
P OVR042 Ovarian Cancer 88 6.013
293
HPT019 Hepatic Encephalopathy 59 6.010
294
HYP060 Hyperinsulinism 54 6.003
295
STT001 Status Epilepticus 59 5.999
296
CHD004 Chudley-Mccullough Syndrome 48 5.983
297
ALL014 Allergic Encephalomyelitis 34 5.965
298
INT323 Intraocular Pressure Quantitative Trait Locus 64 5.943
299
P SCK005 Sickle Cell Disease 56 5.929
300
ACQ007 Acquired Immunodeficiency Syndrome 59 5.925
301
P INT068 Intestinal Disease 53 5.922
302
c HPT016 Hepatitis B 62 5.903
303
SVR004 Severe Combined Immunodeficiency 72 5.888
304
CRV035 Cervical Cancer 73 5.884
305
DBT010 Diabetic Neuropathy 54 5.880
306
CHL123 Chlamydia 58 5.860
307
MNT002 Mental Depression 57 5.845
308
KRT009 Keratosis 53 5.835
309
HYP025 Hyperphosphatemia 48 5.833
310
OTT002 Otitis Media 71 5.822
311
CYN003 Cyanide Poisoning 22 5.799
312
P RTN018 Retinal Disease 53 5.795
313
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 5.787
314
SCH014 Schistosomiasis 56 5.787
315
THY029 Thyroid Carcinoma 51 5.777
316
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 5.771
317
P RHM011 Rheumatoid Arthritis 82 5.758
318
CHG001 Chagas Disease 66 5.755
319
PLG002 Plague 58 5.738
320
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 5.714
321
P EYD002 Eye Disease 57 5.703
322
ADN018 Adenoma 59 5.699
323
BNG077 Benign Idiopathic Neonatal Seizures 23 5.676
324
P PNM007 Pneumonia 67 5.670
325
c PLM128 Pulmonary Hypertension, Primary, 2 28 5.641
326
P TMP001 Temporal Lobe Epilepsy 49 5.639
327
ALL010 Allergic Contact Dermatitis 56 5.625
328
P MLT020 Multiple Sclerosis 79 5.617
329
SFT003 Soft Tissue Sarcoma 57 5.604
330
P EPS003 Episodic Ataxia 59 5.599
331
P SLP006 Sleep Apnea 69 5.583
332
c PLM164 Pulmonary Hypertension, Primary, 1 76 5.563
333
ANG054 Angina Pectoris 66 5.562
334
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 35 5.558
335
P ALP008 Alopecia 54 5.550
336
P PLY019 Polyneuropathy 52 5.515
337
NRT004 Neuritis 53 5.512
338
RTR008 Root Resorption 44 5.512
339
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 5.500
340
P THL005 Thalassemia 56 5.496
341
AVN001 Avian Influenza 61 5.436
342
P ART021 Arteriosclerosis 54 5.418
343
RNL114 Renal Cell Carcinoma, Nonpapillary 80 5.416
344
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 5.412
345
P DNG005 Dengue Virus 56 5.399
346
P ESP024 Esophagitis 60 5.372
347
P SCH015 Schizophrenia 74 5.368
348
GTR002 Goiter 53 5.362
349
ORL011 Oral Cancer 60 5.343
350
ENT011 Enterocolitis 55 5.327
351
PNC041 Pancreatic Ductal Adenocarcinoma 51 5.309
352
P VSC011 Vasculitis 61 5.307
353
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 5.270
354
HLC007 Helicobacter Pylori Infection 67 5.249
355
DNT001 Dental Fluorosis 43 5.247
356
c ACT134 Acute Liver Failure 59 5.231
357
PHN003 Phenylketonuria 76 5.224
358
P GRF003 Graft-Versus-Host Disease 71 5.219
359
NRR001 Neuroretinitis 42 5.218
360
RTN023 Retinitis 46 5.218
361
PNC129 Pancreatic Adenocarcinoma 65 5.214
362
ATS010 Autosomal Recessive Disease 42 5.211
363
HRN029 Hearing Loss, Noise-Induced 37 5.193
364
P ECL001 Eclampsia 52 5.186
365
P TRM003 Tremor 48 5.176
366
NPH003 Nephrocalcinosis 49 5.170
367
P RTN008 Retinitis Pigmentosa 80 5.160
368
MNN043 Meningioma, Familial 79 5.158
369
SCR001 Secretory Meningioma 40 5.158
370
LYM002 Lymphoplasmacyte-Rich Meningioma 35 5.158
371
SPN021 Spinal Meningioma 50 5.158
372
P MYL006 Myeloid Leukemia 61 5.147
373
MDD011 Mood Disorder 62 5.142
374
P MTH007 Methemoglobinemia 46 5.127
375
P BRN022 Bronchiectasis 60 5.122
376
P BNG032 Benign Mesothelioma 53 5.119
377
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 5.117
378
PRP027 Peripheral Vascular Disease 71 5.109
379
DMP001 Dumping Syndrome 43 5.101
380
CRT015 Carotid Artery Occlusion 45 5.082
381
P SPP010 Suppressor of Tumorigenicity 3 51 5.071
382
CRT084 Creatinine Clearance Quantitative Trait Locus 25 5.064
383
GLC003 Glucose Intolerance 54 5.062
384
DPR016 Depression 65 5.046
385
MYL069 Myeloma, Multiple 77 5.033
386
BRN028 Brain Cancer 74 5.029
387
P MSC003 Muscular Atrophy 52 5.025
388
P ART023 Arthropathy 61 5.020
389
P ENC004 Encephalitis 61 5.010
390
THR024 Thrombosis 56 4.980
391
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 4.948
392
P END044 Endometriosis 62 4.935
393
DYS073 Dysphagia 53 4.933
394
PPL022 Papilloma 53 4.931
395
PRM329 Premature Aging 36 4.923
396
VSC002 Vascular Dementia 60 4.911
397
DYS015 Dysentery 50 4.900
398
HNS001 Hansen's Disease 32 4.898
399
RNL077 Renal Fibrosis 46 4.889
400
SQM002 Squamous Cell Papilloma 46 4.877
401
P PRP029 Porphyria 60 4.866
402
P ATS364 Autism 69 4.866
403
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 4.850
404
PRT013 Portal Hypertension 59 4.850
405
SCR003 Secretory Diarrhea 35 4.842
406
ORL015 Oral Squamous Cell Carcinoma 43 4.839
407
OST017 Osteomyelitis 63 4.830
408
P DMN002 Dementia 66 4.787
409
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 4.782
410
DMY004 Demyelinating Disease 50 4.777
411
P MYT002 Myotonic Dystrophy 51 4.775
412
ALL006 Allergic Asthma 56 4.767
413
P HYP061 Hypertrophic Cardiomyopathy 69 4.761
414
MTH009 Mouth Disease 57 4.761
415
c ATS007 Autism Spectrum Disorder 72 4.760
416
DGN001 Degenerative Disc Disease 49 4.741
417
CHL068 Cholestasis 61 4.741
418
PLM134 Pulmonary Fibrosis, Idiopathic 76 4.724
419
P LKM062 Leukemia, Acute Lymphoblastic 69 4.721
420
PST011 Pustulosis of Palm and Sole 52 4.711
421
URT010 Ureteral Obstruction 45 4.707
422
OST011 Osteomalacia 52 4.699
423
ACT209 Acatalasemia 44 4.688
424
CRT072 Creutzfeldt-Jakob Disease 68 4.677
425
PRS045 Prostatic Hypertrophy 53 4.662
426
CRB090 Cerebral Hypoxia 42 4.662
427
CHR178 Chromosomal Triplication 34 4.661
428
LTH043 Lithium Transport 17 4.619
429
c PLM121 Pulmonary Hypertension, Primary, 4 28 4.617
430
LWC001 Low Compliance Bladder 45 4.592
431
c RTN047 Retinitis Pigmentosa 18 46 4.590
432
P SNS001 Sensorineural Hearing Loss 59 4.570
433
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 4.546
434
P RTN024 Retinoblastoma 73 4.540
435
IRN001 Iron Deficiency Anemia 58 4.539
436
PRR019 Perioral Myoclonia with Absences 27 4.536
437
P LPR021 Leprosy 3 71 4.529
438
P PSD003 Pseudohypoaldosteronism 44 4.523
439
P FML023 Familial Hemiplegic Migraine 53 4.514
440
PTT037 Pituitary Tumors 44 4.506
441
P OPT009 Optic Neuritis 57 4.498
442
CND006 Candida Glabrata 30 4.490
443
CHL065 Cholangiocarcinoma 58 4.488
444
INT079 Intrahepatic Cholangiocarcinoma 51 4.488
445
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 4.470
446
RTN003 Retinal Ischemia 49 4.461
447
CRN311 Coronary Ostial Stenosis or Atresia 19 4.459
448
P LPS004 Lupus Erythematosus 61 4.453
449
P MVM001 Movement Disease 61 4.449
450
P PSR002 Psoriasis 63 4.437
451
SDD001 Sudden Infant Death Syndrome 60 4.428
452
P HMP007 Hemophilia 52 4.425
453
PRS047 Prostatitis 58 4.425
454
P LKM002 Leukemia 67 4.410
455
TRG002 Trigeminal Neuralgia 61 4.387
456
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 4.349
457
ANX010 Anxiety 70 4.346
458
P UVT001 Uveitis 57 4.335
459
LYS002 Lysosomal Storage Disease 51 4.329
460
PRN019 Perinatal Necrotizing Enterocolitis 60 4.302
461
P MTR014 Motor Neuron Disease 65 4.291
462
CNN003 Conn's Syndrome 79 4.290
463
GSG001 Gas Gangrene 52 4.284
464
DBT084 Diabetes Mellitus, Ketosis-Prone 60 4.268
465
END057 Endometrial Cancer 72 4.259
466
CHR066 Chronic Fatigue Syndrome 60 4.257
467
THY030 Thyroid Gland Disease 50 4.252
468
LMB062 Limb Ischemia 55 4.245
469
NRM005 Neuromuscular Disease 63 4.235
470
c SYS001 Systemic Lupus Erythematosus 87 4.234
471
BLN006 Blind Loop Syndrome 35 4.232
472
P MLN069 Melanoma, Uveal 61 4.211
473
P THY032 Thyroiditis 57 4.203
474
PRP080 Peripheral Artery Disease 54 4.195
475
CLR109 Colorectal Adenocarcinoma 50 4.186
476
INT066 Interstitial Lung Disease 60 4.179
477
P HDC001 Headache 57 4.171
478
P LKM071 Leukemia, Chronic Lymphocytic 75 4.169
479
HDN002 Head Injury 44 4.169
480
HYP052 Hyperkalemic Periodic Paralysis 63 4.168
481
XRD010 Xeroderma Pigmentosum, Variant Type 73 4.155
482
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 4.153
483
P SCL018 Scoliosis 57 4.147
484
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 4.141
485
WLS001 Wilson Disease 70 4.135
486
c INH020 Inherited Metabolic Disorder 48 4.132
487
P HYD006 Hydrocephalus 61 4.130
488
PRS021 Prostatic Adenoma 43 4.124
489
c SCN007 Secondary Hyperparathyroidism 51 4.109
490
P HYP265 Hypotonia 42 4.107
491
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 4.106
492
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 4.100
493
P BNC003 Bone Cancer 58 4.069
494
P MYS003 Myasthenia Gravis 68 4.066
495
HYP017 Hypophosphatemia 49 4.066
496
c RNG015 Ring Chromosome 2 22 4.061
497
P FRG001 Fragile X Syndrome 70 4.055
498
ILS001 Ileus 50 4.049
499
P NPH012 Nephrotic Syndrome 60 4.048
500
c DWL002 Dowling-Degos Disease 1 58 4.047
501
P KDN017 Kidney Cancer 61 4.040
502
ERL001 Early Myoclonic Encephalopathy 62 4.038
503
PLM001 Pulmonary Tuberculosis 69 4.030
504
P INT143 Interstitial Cystitis 60 4.017
505
P CRD246 Cardiovascular System Disease 56 4.015
506
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.008
507
SCK003 Sickle Cell Anemia 74 3.995
508
P FML011 Familial Adenomatous Polyposis 71 3.993
509
TRN015 Transient Cerebral Ischemia 63 3.993
510
P DYS154 Dystonia 64 3.986
511
c LKM005 Leukemia, T-Cell, Chronic 34 3.981
512
PRS129 Prostatic Hyperplasia, Benign 49 3.980
513
P OPN001 Open-Angle Glaucoma 55 3.971
514
HMG005 Hemoglobinopathy 56 3.965
515
WST005 West Nile Virus 57 3.960
516
P INT070 Intestinal Obstruction 57 3.936
517
P SHR001 Short Bowel Syndrome 53 3.900
518
SLP001 Sleeping Sickness 56 3.899
519
YLL002 Yellow Fever 61 3.881
520
P DBT005 Diabetes Insipidus 54 3.876
521
P RHB003 Rhabdomyosarcoma 66 3.857
522
ACT119 Acute Promyelocytic Leukemia 62 3.851
523
P OBS001 Obstructive Jaundice 48 3.846
524
RTN020 Retinal Vascular Disease 46 3.837
525
GRN017 Granulocytopenia 42 3.835
526
c THY107 Thymoma, Familial 42 3.831
527
P THY023 Thymoma 64 3.831
528
MST021 Meester-Loeys Syndrome 42 3.831
529
P AVS003 Avascular Necrosis 41 3.830
530
P GRV001 Graves' Disease 55 3.822
531
MYC005 Myocardial Stunning 46 3.798
532
SKN019 Skin Melanoma 71 3.795
533
c HMC039 Hemochromatosis, Type 1 73 3.790
534
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 3.778
535
P GCH001 Gaucher's Disease 70 3.752
536
P NRF002 Neurofibromatosis 57 3.749
537
ART016 Aortic Aneurysm 68 3.746
538
c HNT011 Huntington Disease-Like 3 34 3.737
539
TRY001 Trypanosomiasis 50 3.724
540
MSC007 Muscle Hypertrophy 64 3.722
541
P CNJ013 Conjunctivitis 66 3.706
542
P MNC007 Monocytic Leukemia 47 3.701
543
BCT004 Bacteriuria 47 3.691
544
P MYP006 Myopia 56 3.690
545
P TRN020 Turner Syndrome 67 3.672
546
P LYM118 Lymphoma 67 3.670
547
AMN003 Amnestic Disorder 54 3.669
548
c OPT053 Optic Atrophy 1 62 3.668
549
P MGR003 Migraine with Aura 52 3.660
550
ATN005 Autonomic Dysfunction 46 3.658
551
BRR014 Barrett Esophagus 66 3.656
552
FBR047 Fibromyalgia 58 3.654
553
P SLM003 Salmonellosis 54 3.650
554
c LNG048 Long Qt Syndrome 3 53 3.645
555
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.643
556
SPP011 Suppression of Tumorigenicity 12 61 3.634
557
P ASP006 Aspergillosis 72 3.633
558
RTN017 Retinal Detachment 60 3.630
559
P EXN002 Exanthem 58 3.626
560
SPS057 Spasticity 42 3.614
561
P MNN013 Meningitis 65 3.601
562
EXT007 Extracutaneous Mastocytoma 38 3.596
563
MST004 Mast Cell Neoplasm 42 3.596
564
KRT006 Keratoconjunctivitis 53 3.595
565
PLM033 Pulmonary Embolism 58 3.582
566
P SYS005 Systemic Scleroderma 74 3.579
567
KRT071 Keratosis, Seborrheic 56 3.571
568
INV005 Inverted Follicular Keratosis 32 3.571
569
PRP030 Purpura 54 3.567
570
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 3.567
571
MSL001 Measles 61 3.560
572
ART002 Arts Syndrome 66 3.557
573
SPL018 Splenomegaly 49 3.543
574
c HPT003 Hepatitis a 63 3.539
575
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 3.536
576
P MTC069 Mitochondrial Disorders 57 3.520
577
P SLP005 Sleep Disorder 61 3.517
578
P NRV007 Nervous System Disease 67 3.515
579
PLC002 Plica Syndrome 35 3.515
580
SYN007 Synovitis 55 3.515
581
P NGH001 Night Blindness 52 3.505
582
c LKM063 Leukemia, Chronic Myeloid 71 3.499
583
P HMC002 Homocystinuria 53 3.498
584
PRP016 Paraplegia 52 3.498
585
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 57 3.496
586
P ATR005 Atrophic Gastritis 50 3.486
587
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 22 3.485
588
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 3.480
589
LYM017 Lyme Disease 62 3.477
590
P ATT013 Attention Deficit-Hyperactivity Disorder 64 3.475
591
c SCL052 Scleroderma, Familial Progressive 61 3.471
592
P PRD017 Periodic Paralyses 24 3.470
593
CHL004 Cholelithiasis 49 3.468
594
MLD018 Mild Cognitive Impairment 48 3.453
595
ACT003 Acute Kidney Tubular Necrosis 46 3.445
596
P HYP750 Hypertriglyceridemia, Familial 62 3.438
597
INT007 Intermediate Coronary Syndrome 54 3.428
598
LYM133 Lymphoma, Hodgkin, Classic 74 3.422
599
BLR008 Bilirubin Metabolic Disorder 57 3.418
600
NWC001 Newcastle Disease 47 3.412
601
GNT046 Genetic Epilepsy with Febrile Seizures Plus 29 3.407
602
VGN023 Vaginitis 56 3.407
603
DDN004 Duodenogastric Reflux 31 3.403
604
ANR040 Aneurysm 61 3.401
605
c SCN036 Secondary Progressive Multiple Sclerosis 55 3.400
606
EMB004 Embryonal Carcinoma 56 3.398
607
LNG031 Lung Benign Neoplasm 51 3.396
608
BRN056 Bronchopulmonary Dysplasia 56 3.385
609
c RNG019 Ring Chromosome 3 19 3.379
610
MST020 Mast Cell Activation Syndrome 28 3.376
611
KLB003 Klebsiella Pneumonia 50 3.375
612
CHR074 Choriocarcinoma 46 3.374
613
PLM031 Poliomyelitis 63 3.367
614
CHK001 Chikungunya 60 3.359
615
ENM002 Enamel Erosion 25 3.357
616
MTC005 Mitochondrial Metabolism Disease 45 3.357
617
RBS001 Rabies 58 3.350
618
P RNV001 Renovascular Hypertension 49 3.350
619
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 3.348
620
BRK010 Burkitt Lymphoma 66 3.343
621
P PYL005 Pyelonephritis 57 3.330
622
LYM143 Lymphoma, Non-Hodgkin, Familial 75 3.329
623
HPT022 Hepatoblastoma 54 3.318
624
c HNT004 Huntington Disease-Like 2 52 3.315
625
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 3.313
626
c ACT249 Acute Asthma 40 3.308
627
c MST023 Mesothelioma, Malignant 56 3.307
628
ENC055 Encephalopathy, Ethylmalonic 51 3.306
629
OCL006 Ocular Hypertension 53 3.299
630
P ART005 Arteriovenous Malformation 65 3.299
631
P FML187 Familial Hypertension 34 3.289
632
P END033 Endocarditis 58 3.276
633
BRC012 Brucellosis 66 3.274
634
VSC003 Visceral Leishmaniasis 55 3.273
635
CRD137 Cardiogenic Shock 56 3.261
636
PTH003 Pathologic Nystagmus 52 3.260
637
CHC001 Chickenpox 57 3.260
638
CRV040 Cervix Carcinoma 50 3.254
639
P BRT004 Bartter Disease 58 3.248
640
SQM013 Squamous Cell Carcinoma, Head and Neck 73 3.242
641
VLV047 Volvulus of Midgut 52 3.241
642
c PRM005 Primary Hyperparathyroidism 59 3.237
643
SLC006 Silicosis 56 3.236
644
P LKD001 Leukodystrophy 59 3.223
645
ENT004 Enthesopathy 51 3.211
646
P THR014 Thrombocytopenia 66 3.204
647
LBR035 Liberfarb Syndrome 27 3.203
648
PLS007 Plasmodium Falciparum Malaria 52 3.201
649
EPT021 Epithelial Recurrent Erosion Dystrophy 46 3.195
650
HMP005 Hemiplegia 54 3.191
651
MYL013 Myeloperoxidase Deficiency 44 3.191
652
P SRC025 Sarcoidosis 1 71 3.182
653
P MCR129 Microvascular Complications of Diabetes 1 68 3.181
654
c MCR112 Microvascular Complications of Diabetes 2 42 3.181
655
GLC022 Glucose/galactose Malabsorption 44 3.181
656
GST040 Gastric Adenocarcinoma 67 3.180
657
CMM005 Common Cold 56 3.180
658
P MCL001 Mucolipidosis 49 3.172
659
P RNL115 Renal Tubular Acidosis, Proximal 32 3.160
660
c GLC092 Glaucoma, Primary Open Angle 62 3.154
661
c HMP004 Hemophilia B 68 3.151
662
P CHL066 Cholangitis 52 3.150
664
P GLL018 Gallbladder Cancer 53 3.138
665
P FRD001 Friedreich Ataxia 61 3.128
666
GLM044 Glomerular Disease 35 3.117
667
HRT011 Heart Septal Defect 49 3.111
668
TRN018 Transitional Cell Carcinoma 56 3.109
669
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 55 3.099
670
MMM001 Mammary Paget's Disease 53 3.099
671
EWN003 Ewing Sarcoma 70 3.098
672
SBC016 Subacute Delirium 43 3.092
673
P NTR004 Neutropenia 63 3.088
674
P HYP097 Hyperekplexia 62 3.077
675
P TCD001 Tic Disorder 49 3.076
676
URN010 Urinary Tract Obstruction 55 3.075
677
c HMP029 Hemophilia a 68 3.074
678
INF034 Infective Endocarditis 54 3.066
679
P HYP098 Hypereosinophilic Syndrome 66 3.059
680
c CHR417 Chronic Graft Versus Host Disease 55 3.058
681
PRM057 Paramyotonia Congenita of Von Eulenburg 59 3.043
682
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 3.041
683
TYP007 Typhoid Fever 64 3.035
684
PCD001 Pica Disease 38 3.030
685
NPH018 Nephrogenic Systemic Fibrosis 49 3.027
686
BRN002 Bronchiolitis 57 3.027
687
P MCR010 Microcephaly 60 3.023
688
ECH003 Echinococcosis 53 3.008
689
CYN002 Cyanosis, Transient Neonatal 43 3.006
690
P URT039 Urticaria 58 2.996
691
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.994
692
P MTH008 Methylmalonic Acidemia 52 2.992
693
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 2.989
694
CHR073 Choreatic Disease 54 2.989
695
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 2.986
696
FCT001 Factor Viii Deficiency 60 2.981
697
c THR092 Thrombophilia Due to Thrombin Defect 74 2.977
698
P MJR007 Major Affective Disorder 1 42 2.976
699
P RTT002 Rett Syndrome 79 2.968
700
P FML340 Familial Episodic Pain Syndrome 50 2.962
701
HRT012 Heart Valve Disease 53 2.962
702
BNG006 Benign Familial Neonatal Epilepsy 55 2.961
703
PRC003 Proctitis 49 2.958
704
c FML021 Familial Hypercholesterolemia 72 2.957
705
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 2.954
706
P RRT020 Rare Tumor 39 2.950
707
CRB037 Cerebral Palsy 67 2.948
708
P EPL140 Epilepsy, Idiopathic Generalized 62 2.944
709
GNG003 Gingival Recession 49 2.941
710
PRQ002 Paraquat Poisoning 28 2.929
711
TNG007 Tongue Carcinoma 52 2.927
712
CLN019 Colonic Disease 47 2.925
713
PRX001 Peroxisomal Disease 46 2.925
714
P RTN022 Retinal Vein Occlusion 54 2.924
715
c BTT014 Beta-Thalassemia 72 2.912
716
MLT006 Multidrug-Resistant Tuberculosis 47 2.912
717
EXR010 Exercise-Induced Bronchoconstriction 34 2.907
718
GST019 Gastrointestinal Stromal Tumor 78 2.885
719
GTL001 Gitelman Syndrome 65 2.883
720
CNN005 Connective Tissue Disease 67 2.881
721
CNT057 Central Centrifugal Cicatricial Alopecia 36 2.878
722
MCR013 Microphthalmia 60 2.874
723
NRL016 Neural Tube Defects 81 2.873
724
MCP006 Mucoepidermoid Carcinoma 48 2.866
725
HRD218 Hereditary Stomatocytosis 30 2.864
726
P LRY044 Larynx Cancer 54 2.859
727
DWR001 Dwarfism 44 2.845
728
PLC008 Placenta Disease 49 2.841
729
VGN019 Vaginal Discharge 47 2.834
730
SHG001 Shigellosis 63 2.825
731
TNP004 Tn Polyagglutination Syndrome 42 2.824
732
PRS063 Paresthesia 39 2.823
733
P VNS003 Venous Insufficiency 55 2.817
734
GRD001 Giardiasis 46 2.815
735
PHR003 Pharyngitis 58 2.813
736
TRT001 Teratocarcinoma 42 2.805
737
DSS010 Dissociative Disorder 39 2.801
738
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 47 2.801
739
ORL005 Oral Candidiasis 56 2.801
740
FDL002 Food Allergy 47 2.797
741
CHR576 Chronic Beryllium Disease 42 2.788
742
P BRY005 Beryllium Disease 39 2.788
743
CMP034 Complete Androgen Insensitivity Syndrome 55 2.787
744
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 19 2.780
745
P RBL001 Rubella 58 2.778
746
VTM002 Vitamin B12 Deficiency 48 2.773
747
HSH003 Hashimoto Thyroiditis 60 2.768
748
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 2.765
749
DNG003 Dengue Disease 65 2.761
750
P VTR007 Vitreoretinopathy 46 2.760
751
c BCT007 Bacterial Meningitis 55 2.752
752
MNN028 Mononeuropathy of the Median Nerve, Mild 46 2.750
753
IGR001 Ige Responsiveness, Atopic 59 2.749
754
P RNL015 Renal Hypertension 45 2.745
755
HRY003 Hairy Cell Leukemia 61 2.744
756
LCH001 Leech Infestation 38 2.742
757
STL007 Steel Syndrome 42 2.734
758
P TXP001 Toxoplasmosis 60 2.732
759
ADL002 Adult Syndrome 70 2.729
760
CRB086 Cerebral Aneurysms 40 2.729
761
P INS002 in Situ Carcinoma 53 2.728
762
GST033 Gestational Diabetes 61 2.727
763
WRN001 Werner Syndrome 69 2.727
764
HYP457 Hypertrophic Scars 42 2.723
765
KRT002 Keratomalacia 55 2.722
766
P ANR048 Aniridia 1 64 2.713
767
P GLL022 Guillain-Barre Syndrome 60 2.705
768
P SBS003 Substance Abuse 54 2.702
769
DSS009 Disseminated Intravascular Coagulation 57 2.701
770
ANR007 Anorexia Nervosa 60 2.697
771
c MLG084 Malignant Fibrous Histiocytoma 62 2.695
772
P OST001 Osteopetrosis 71 2.691
773
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 2.690
774
CNT105 Central Core Disease of Muscle 59 2.688
775
ATN004 Autonomic Neuropathy 42 2.686
776
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 2.684
777
FCL014 Focal Epilepsy 53 2.676
778
OCC016 Occupational Asthma 33 2.674
779
c SVR005 Severe Pre-Eclampsia 50 2.662
780
c BCT013 Bacterial Pneumonia 48 2.661
781
c EXD008 Exudative Vitreoretinopathy 1 71 2.659
782
c CNG006 Congenital Hypothyroidism 63 2.651
783
P CHR071 Charcot-Marie-Tooth Disease 64 2.649
784
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 2.644
785
FLR002 Filariasis 55 2.635
786
VLK001 Volkmann Contracture 23 2.632
787
P KRT007 Keratoconus 50 2.629
788
P TBR001 Tuberous Sclerosis 69 2.629
789
AST006 Astigmatism 47 2.625
790
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 2.624
791
P MDL005 Medulloblastoma 75 2.623
792
IGG001 Iga Glomerulonephritis 50 2.622
793
P ACT105 Acute Mountain Sickness 52 2.622
794
PPT001 Peptic Esophagitis 52 2.621
795
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 27 2.612
796
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 55 2.608
797
P HYP024 Hypoparathyroidism 55 2.607
798
P CRN026 Corneal Edema 42 2.607
799
P FBR003 Fibrous Histiocytoma 43 2.603
800
PRP083 Porphyria, Acute Intermittent 65 2.600
801
RHB024 Rhabdomyosarcoma 2 67 2.598
802
BLC012 Bile Acid Malabsorption, Primary 44 2.594
803
P PRM002 Primary Hyperoxaluria 65 2.592
804
ACH005 Achalasia 55 2.592
805
ACN019 Acanthamoeba Keratitis 30 2.589
806
P HMR005 Hemorrhoid 49 2.577
807
CLS016 Clostridium Difficile Colitis 49 2.570
808
c FNC027 Fanconi Anemia, Complementation Group a 81 2.569
809
P PNC025 Panic Disorder 52 2.569
810
ADG002 Audiogenic Seizures 25 2.567
811
FRN006 Frontotemporal Dementia 68 2.564
812
KWS001 Kwashiorkor 45 2.562
813
KWS002 Kawasaki Disease 65 2.561
814
P NJM001 Nijmegen Breakage Syndrome 76 2.559
815
CRY003 Cryptosporidiosis 56 2.552
816
FBR012 Fabry Disease 70 2.545
817
P PRP003 Porphyria Cutanea Tarda 66 2.539
818
ART004 Aortic Atherosclerosis 47 2.538
819
AZS001 Azoospermia 45 2.533
820
P PLM034 Pulmonary Emphysema 58 2.532
821
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 2.531
822
P XRD029 Xeroderma Pigmentosum, Complementation Group a 56 2.528
823
CCN002 Cocaine Abuse 49 2.525
824
P VNW001 Von Willebrand's Disease 65 2.519
825
P EPL198 Epilepsy, Myoclonic Juvenile 61 2.513
826
PRM013 Premature Menopause 58 2.511
827
P DNT007 Dentin Sensitivity 34 2.509
828
DRM046 Dermal Ridges-off-the-End 20 2.503
829
MLT157 Multiple System Atrophy 1 69 2.502
830
OST115 Osteonecrosis of the Jaw 41 2.501
831
THY128 Thyroid Tumor 35 2.501
832
WTH001 Withdrawal Disorder 48 2.500
833
P MYC033 Myoclonus 47 2.495
834
P PNM006 Pneumoconiosis 55 2.494
835
ANT018 Anthracosis 51 2.494
836
CMB007 Combined Immunodeficiency 57 2.493
837
CCC002 Coccidiosis 50 2.492
838
CLR030 Clear Cell Renal Cell Carcinoma 54 2.486
839
NRT001 Neurotic Disorder 56 2.484
840
ENM001 Enamel Caries 27 2.483
841
LPT001 Leptospirosis 66 2.478
842
JPN002 Japanese Encephalitis 61 2.476
843
RNL011 Renal Osteodystrophy 49 2.476
844
CTN007 Cutaneous Leishmaniasis 62 2.473
845
c ACT073 Acute Leukemia 58 2.473
846
ACR007 Acromegaly 70 2.470
847
BRT054 Brittle Bone Disorder 74 2.466
848
PRC002 Paracoccidioidomycosis 54 2.463
849
P CMP008 Compartment Syndrome 50 2.462
850
RDT005 Radiation Induced Cancer 21 2.454
851
ALB002 Albinism 47 2.451
852
TTH006 Tooth Disease 51 2.450
853
c VRL010 Viral Hepatitis 53 2.445
854
OCL022 Ocular Melanoma 52 2.445
855
c JVN010 Juvenile Rheumatoid Arthritis 66 2.445
856
P TYR004 Tyrosinemia 50 2.444
857
SMT004 Smith-Lemli-Opitz Syndrome 70 2.444
858
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 2.443
859
c PRG042 Progressive Familial Heart Block, Type Ia 66 2.442
860
ETN001 Eating Disorder 59 2.435
861
c BSL007 Basal Cell Carcinoma 68 2.432
862
OPD006 Opioid Addiction 48 2.430
863
WLL004 Wallerian Degeneration 38 2.430
864
CRC021 Carcinosarcoma 64 2.429
865
P MTC133 Mitochondrial Myopathy 50 2.428
866
RFR003 Refractive Error 41 2.428
867
GST037 Gastroparesis 52 2.424
868
P FCL005 Focal Segmental Glomerulosclerosis 57 2.422
869
P ACT008 Actinic Keratosis 54 2.422
870
CRV038 Cervical Squamous Cell Carcinoma 58 2.421
871
P CHN059 Chondrocalcinosis 52 2.409
872
P SYP003 Syphilis 59 2.408
873
LPT014 Leptin Deficiency or Dysfunction 78 2.405
874
P GLY013 Glycogen Storage Disease 60 2.397
875
CYS019 Cystathioninuria 46 2.392
876
c ART115 Aortic Valve Disease 1 74 2.392
877
c SPR086 Spermatogenic Failure 3 46 2.391
878
PLS011 Plasmacytoma 56 2.387
879
PLR007 Pleural Empyema 51 2.384
880
c TBR025 Tuberous Sclerosis 1 84 2.374
881
P GLC113 Galactosemia I 66 2.374
882
NRM001 Neuromyelitis Optica 61 2.373
883
P LCH002 Lichen Planus 54 2.371
884
P NMN002 Niemann-Pick Disease 60 2.370
885
ANR004 Anuria 44 2.368
886
P ATR010 Atrial Heart Septal Defect 58 2.366
887
JMP002 Jumping Frenchmen of Maine 21 2.364
888
CRN027 Corneal Neovascularization 47 2.363
889
P CRV039 Cervicitis 52 2.358
890
SML019 Smallpox 55 2.348
891
APP008 Appendicitis 62 2.344
892
IDP073 Idiopathic Hypercalciuria 40 2.343
893
P LPS002 Liposarcoma 64 2.339
894
c PNS012 Paine Syndrome 60 2.339
895
P ZLL001 Zellweger Syndrome 65 2.336
896
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 2.331
897
P CRC039 Coarctation of Aorta 46 2.331
898
MYC014 Mycobacterium Chelonae 29 2.331
899
IDP070 Idiopathic Scoliosis 42 2.329
900
OBS082 Obstructive Nephropathy 41 2.323
901
FNC002 Functional Diarrhea 40 2.323
902
P SJG008 Sjogren Syndrome 61 2.321
903
P BRB001 Beriberi 44 2.321
904
RTC003 Root Caries 32 2.318
905
SPN051 Spondylitis 51 2.318
906
INF009 Inflammatory Spondylopathy 30 2.318
907
P MYS005 Myositis 56 2.317
908
HYP006 Hypertensive Heart Disease 49 2.315
909
KLD004 Keloid Disorder 39 2.315
910
ALC006 Alcoholic Hepatitis 61 2.314
912
P HYP120 Hypoaldosteronism 35 2.310
913
P APL001 Aplastic Anemia 73 2.304
915
HMG002 Hemoglobinuria 50 2.303
916
LST001 Listeriosis 59 2.296
917
P HRD011 Hereditary Spherocytosis 64 2.295
918
PLY100 Polyploidy 36 2.294
919
LYM027 Lymphopenia 56 2.289
920
P MPL001 Maple Syrup Urine Disease 70 2.289
921
BCK006 Back Pain 47 2.287
922
P SCL057 Scoliosis, Isolated 1 40 2.285
923
HTC003 Hutchinson-Gilford Progeria Syndrome 65 2.285
924
RYN005 Raynaud Phenomenon 45 2.281
925
P PRL003 Proliferative Glomerulonephritis 43 2.274
926
TNG009 Tongue Squamous Cell Carcinoma 43 2.270
927
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 64 2.269
928
CYS013 Cystinuria 66 2.268
929
LNG039 Lung Squamous Cell Carcinoma 57 2.265
930
CHR431 Chronic Venous Insufficiency 48 2.265
931
DBT007 Diabetic Cataract 36 2.264
932
LYM009 Lymphocytic Choriomeningitis 46 2.263
933
SCH038 Schopf-Schulz-Passarge Syndrome 51 2.262
934
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 2.262
935
HRT015 Heritable Pulmonary Arterial Hypertension 46 2.261
936
P FNC004 Fanconi Syndrome 60 2.261
937
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 2.258
938
CNT060 Central Serous Chorioretinopathy 38 2.257
939
HMM004 Hamamy Syndrome 39 2.253
940
VRL003 Variola Major 43 2.252
941
c GRV008 Graves Disease 1 54 2.252
942
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 2.249
943
c SPN225 Spondyloarthropathy 1 70 2.248
944
CNT016 Central Retinal Vein Occlusion 54 2.248
945
P FTL001 Fetal Alcohol Syndrome 55 2.248
946
EXC002 Exocrine Pancreatic Insufficiency 42 2.248
947
FLR001 Filarial Elephantiasis 59 2.247
948
c HPT007 Hepatitis E 51 2.238
949