Search results for Chloride ion

2519 hits were found for Chloride ion

# Family MCID Name MIFTS Score
1
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 63.001
2
CYS001 Cystic Fibrosis 78 45.060
3
DRR008 Diarrhea 1, Secretory Chloride, Congenital 51 41.923
4
CNG064 Congenital Chloride Diarrhea 34 37.735
5
HRW001 Hair Whorl 35 32.428
6
P BRN076 Bronchiectasis with or Without Elevated Sweat Chloride 1 33 31.931
7
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 27.546
8
MTB004 Metabolic Acidosis 48 26.552
9
RPD005 Rapidly Involuting Congenital Hemangioma 46 26.350
10
HLX001 Helix Syndrome 48 25.827
11
HYP005 Hypokalemia 55 22.286
12
48X005 48,xyyy 39 20.557
13
HYP266 Hypoxia 57 19.652
14
c DNT047 Dentinogenesis Imperfecta Type 2 35 19.506
15
P DRR001 Diarrhea 55 18.900
16
c HYP595 Hypertension, Essential 85 17.918
17
ALL029 Allergic Disease 59 17.840
18
P NRB001 Neuroblastoma 66 17.698
19
P ANP001 Anaplastic Large Cell Lymphoma 61 17.484
20
MYT011 Myotonia 39 17.169
21
CHL014 Cholera 62 17.146
22
PRT037 Pertussis 65 16.676
23
c ACT071 Acute Kidney Failure 60 16.547
24
P KDN018 Kidney Disease 72 16.296
25
c PSD092 Pseudohypoaldosteronism, Type Iie 48 15.937
26
LNG099 Lung Disease 62 15.931
27
GLL048 Glial Tumor 52 15.683
28
GLM045 Glioma 63 15.639
29
ISC004 Ischemia 61 15.284
30
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 15.262
31
P LNG028 Long Qt Syndrome 64 15.104
32
ANX004 Anoxia 40 14.956
33
NPH009 Nephrolithiasis 54 14.588
34
GLB002 Glioblastoma 67 14.322
35
c CHR684 Chronic Kidney Disease 69 14.078
36
P EPL164 Epilepsy 68 13.953
37
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 13.888
38
CRB004 Cerebral Artery Occlusion 45 13.771
39
CNT047 Contact Dermatitis 57 13.750
40
BNR002 Bone Resorption Disease 47 13.707
41
P SZR006 Seizure Disorder 70 13.374
42
PPL052 Papillomatosis, Confluent and Reticulated 34 13.328
43
LWC001 Low Compliance Bladder 45 13.274
44
P RNL007 Renal Tubular Acidosis 50 13.199
45
P ALZ034 Alzheimer Disease 87 12.924
46
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 12.875
47
P BRT004 Bartter Disease 58 12.773
48
ISL119 Isolated Optic Neuritis 26 12.738
49
OST159 Osteogenic Sarcoma 66 12.422
50
CNG034 Congestive Heart Failure 69 12.388
51
P PRS040 Prostate Cancer 95 12.291
52
CRD132 Cardiac Conduction Defect 60 12.267
53
ATS010 Autosomal Recessive Disease 42 12.228
54
P BPL003 Bipolar Disorder 56 12.224
55
P CHR345 Chronic Pain 50 12.142
56
c MJR022 Major Affective Disorder 8 38 12.113
57
c MJR024 Major Affective Disorder 9 41 12.113
58
P MYT023 Myotonia Congenita 55 12.091
59
P PNC035 Pancreatic Cancer 86 11.791
60
c BRN108 Branchiootic Syndrome 1 62 11.768
61
AGN016 Aging 54 11.760
62
c MGR028 Migraine with or Without Aura 1 64 11.723
63
ANG020 Angiosarcoma 64 11.701
64
47X002 47,xyy 48 11.642
65
CNS004 Constipation 56 11.612
66
P HYP069 Hyperparathyroidism 62 11.591
67
P PLY014 Polycystic Kidney Disease 69 11.541
68
P CRD119 Cardiac Arrest 67 11.441
69
SCR003 Secretory Diarrhea 35 11.416
70
CYT002 Cytokine Deficiency 43 11.371
71
P LTR001 Lateral Sclerosis 58 11.338
72
c AMY091 Amyotrophic Lateral Sclerosis 1 88 11.272
73
SPN186 Spinal Cord Injury 61 11.122
74
BRN004 Brain Edema 54 11.112
75
DNT012 Dental Caries 53 11.103
76
PNG002 Pain Agnosia 51 11.085
77
P PRD021 Periodic Paralysis 41 10.926
78
TXC005 Toxic Shock Syndrome 62 10.915
79
DRM006 Dermatitis 62 10.893
80
PRT251 Proteinuria, Chronic Benign 57 10.883
81
CRD223 Cardiac Arrhythmia 63 10.792
82
P PHC003 Pheochromocytoma 69 10.761
83
ADR040 Adrenal Gland Pheochromocytoma 46 10.761
84
IRN002 Iron Metabolism Disease 57 10.705
85
PST092 Posttransplant Acute Limbic Encephalitis 28 10.649
86
BRN071 Brain Injury 50 10.638
87
URL001 Urolithiasis 46 10.607
88
BCT022 Bacterial Infectious Disease 56 10.522
89
GTL001 Gitelman Syndrome 65 10.520
90
P HPT023 Hepatocellular Carcinoma 96 10.513
91
ALL010 Allergic Contact Dermatitis 56 10.496
92
P MYC007 Myocardial Infarction 70 10.486
93
P ENC018 Encephalopathy 62 10.483
94
P NSP012 Nasopharyngeal Carcinoma 61 10.442
95
HYP066 Hyperglycemia 61 10.427
96
P MLN008 Melanoma 76 10.330
97
P INF032 Infertility 57 10.324
98
GNG013 Gingivitis 59 10.316
99
PLM010 Pulmonary Edema 55 10.239
100
BRN024 Bronchitis 67 10.234
101
INT323 Intraocular Pressure Quantitative Trait Locus 64 10.220
102
P PRD008 Periodontitis 64 10.198
103
P NRP001 Neuropathy 60 10.177
104
P RSP003 Respiratory Failure 74 10.152
105
TRM010 Traumatic Brain Injury 51 10.144
106
OST012 Osteoarthritis 77 10.097
107
OCL069 Ocular Motor Apraxia 57 10.080
108
P LNG032 Lung Cancer 98 9.982
109
CNN003 Conn's Syndrome 79 9.962
110
NPH091 Nephrolithiasis, Calcium Oxalate 61 9.926
111
P HRT032 Heart Disease 81 9.871
112
PLM129 Pulmonary Disease, Chronic Obstructive 74 9.871
113
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 9.850
114
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 9.846
115
P BND020 Bone Disease 59 9.839
116
SVR001 Severe Acute Respiratory Syndrome 67 9.743
117
NPH003 Nephrocalcinosis 49 9.566
118
HMN044 Human Immunodeficiency Virus Type 1 78 9.476
119
ADN018 Adenoma 59 9.466
120
P ADN016 Adenocarcinoma 63 9.459
121
P MSC005 Muscular Dystrophy 67 9.369
122
P INF038 Influenza 68 9.363
123
END086 End Stage Renal Disease 52 9.318
124
PLY150 Polykaryocytosis Inducer 29 9.298
125
c PLM127 Pulmonary Hypertension, Primary, 3 34 9.276
126
c ACT027 Acute Pancreatitis 60 9.270
127
P MRC003 Mercury Poisoning 49 9.234
128
TTN003 Tetanus 65 9.184
129
DFC004 Deficiency Anemia 74 9.173
130
RCK004 Rickets 68 9.170
131
P DST107 Distal Renal Tubular Acidosis 48 9.158
132
P RHN004 Rhinitis 57 9.126
133
P ATR011 Atrial Fibrillation 66 9.099
134
P GLM040 Glioma Susceptibility 1 71 9.080
135
ATM095 Autoimmune Disease 61 9.078
136
P DRM053 Dermatitis, Atopic 65 9.059
137
P PNC044 Pancreatitis 61 9.054
138
P GST044 Gastritis 55 9.038
139
P CTR002 Cataract 60 9.011
140
P BRS047 Breast Cancer 98 8.996
141
c PRC016 Pre-Eclampsia 65 8.951
142
HMS001 Hemosiderosis 48 8.938
143
DPH001 Diphtheria 59 8.932
144
SQM006 Squamous Cell Carcinoma 60 8.876
145
P MYC084 Mycobacterium Tuberculosis 1 68 8.849
146
CLT003 Colitis 63 8.836
147
P TRM003 Tremor 48 8.825
148
LVR012 Liver Cirrhosis 63 8.806
149
c HYP836 Hypercholesterolemia, Familial, 1 73 8.803
150
ALC007 Alcohol Dependence 66 8.780
151
P BRN022 Bronchiectasis 60 8.748
152
P AST005 Asthma 76 8.744
153
P PSD003 Pseudohypoaldosteronism 44 8.678
154
SKN016 Skin Disease 63 8.635
155
STT001 Status Epilepticus 59 8.594
156
IRR002 Irritable Bowel Syndrome 65 8.581
157
DWN001 Down Syndrome 70 8.577
158
BRN028 Brain Cancer 74 8.541
159
P PLM037 Pulmonary Hypertension 72 8.519
160
P TMP001 Temporal Lobe Epilepsy 49 8.494
161
P LNG064 Lung Cancer Susceptibility 3 70 8.494
162
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 8.468
163
ARG004 Argyria 26 8.447
164
c ACT075 Acute Myocardial Infarction 56 8.425
165
P LVR013 Liver Disease 69 8.408
166
c ATR087 Atrial Standstill 1 74 8.355
167
P MYP004 Myopathy 67 8.314
168
CHR072 Chordoma 57 8.299
169
MDD018 Middle East Respiratory Syndrome 44 8.295
170
P MYS003 Myasthenia Gravis 68 8.276
171
P URN019 Urinary Tract Infection 49 8.266
172
P MLN007 Male Infertility 56 8.254
173
P RRH023 Rare Hereditary Hemochromatosis 54 8.188
174
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 8.166
175
c ACT068 Acute Cystitis 61 8.161
176
P HRP006 Herpes Simplex 65 8.156
177
HYP056 Hypoglycemia 65 8.082
178
P PRK039 Parkinsonism 55 8.081
179
P HNT016 Huntington Disease 73 8.050
180
P HPT021 Hepatitis 69 8.030
181
P MYT002 Myotonic Dystrophy 51 8.013
182
ATH013 Atherosclerosis Susceptibility 63 7.983
183
P BRG001 Brugada Syndrome 69 7.983
184
CRT084 Creatinine Clearance Quantitative Trait Locus 25 7.966
185
P ADL010 Adult Respiratory Distress Syndrome 71 7.956
186
MCS002 Mucositis 56 7.947
187
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 7.930
188
P INF037 Inflammatory Bowel Disease 53 7.904
189
HPT004 Hepatic Coma 43 7.850
190
SRC014 Sarcoma 65 7.845
191
MLG169 Malignant Astrocytoma 57 7.841
192
SPN035 Spindle Cell Sarcoma 54 7.821
193
CRV035 Cervical Cancer 73 7.814
194
P BCL017 B-Cell Lymphoma 59 7.800
195
MDD011 Mood Disorder 62 7.795
196
P GLM007 Glomerulonephritis 60 7.794
197
P OPN001 Open-Angle Glaucoma 55 7.771
198
SYN036 Syncope 45 7.768
199
P CHN012 Chondrosarcoma 57 7.767
200
P VSC007 Vascular Disease 63 7.759
201
c MCR130 Microvascular Complications of Diabetes 6 41 7.759
202
c MCR120 Microvascular Complications of Diabetes 7 47 7.759
203
c MCR113 Microvascular Complications of Diabetes 3 52 7.759
204
c MCR133 Microvascular Complications of Diabetes 4 41 7.759
205
NNL005 Non-Alcoholic Fatty Liver Disease 63 7.737
206
FTT001 Fatty Liver Disease 62 7.735
207
c HPT073 Hepatitis C Virus 71 7.727
209
P OST002 Osteoporosis 76 7.701
210
P HYP086 Hypothyroidism 69 7.698
211
c SML038 Small Cell Cancer of the Lung 69 7.693
212
THR024 Thrombosis 56 7.686
213
P INT070 Intestinal Obstruction 57 7.665
214
P OVR042 Ovarian Cancer 88 7.631
215
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 7.613
216
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 7.613
217
P OVR082 Overgrowth Syndrome 49 7.579
218
P PLM036 Pulmonary Fibrosis 66 7.561
219
P PRP019 Peripheral Nervous System Disease 58 7.533
220
GST045 Gastroenteritis 58 7.518
221
PRT036 Peritonitis 65 7.496
222
HPT019 Hepatic Encephalopathy 59 7.492
223
ANT024 Anthrax Disease 58 7.481
224
P LCT001 Lactic Acidosis 51 7.472
225
P PRK057 Parkinson Disease, Late-Onset 80 7.464
226
STR067 Stroke, Ischemic 80 7.454
227
SVR004 Severe Combined Immunodeficiency 72 7.411
228
P FBR017 Fibrosarcoma 56 7.406
229
P KLZ004 Kala-Azar 1 41 7.405
230
LSH001 Leishmaniasis 64 7.405
231
VCC001 Vaccinia 47 7.379
232
ALL003 Allergic Rhinitis 67 7.356
233
P SCH015 Schizophrenia 74 7.344
234
P OST001 Osteopetrosis 71 7.332
235
HYP025 Hyperphosphatemia 48 7.317
236
P OPT006 Optic Nerve Disease 58 7.300
237
P DNT020 Dent Disease 1 63 7.294
238
c HPT001 Hepatitis C 62 7.273
239
URM002 Uremia 47 7.253
240
P AMY004 Amyloidosis 70 7.244
241
PRS047 Prostatitis 58 7.217
242
c TYP009 Type 2 Diabetes Mellitus 92 7.216
243
PPT005 Peptic Ulcer Disease 58 7.215
244
P GST053 Gastric Cancer 83 7.198
245
GTR002 Goiter 53 7.195
246
P EYD002 Eye Disease 57 7.170
247
ULC004 Ulcerative Colitis 74 7.163
248
P EPS003 Episodic Ataxia 59 7.085
249
P DBT005 Diabetes Insipidus 54 7.068
250
P SKN015 Skin Carcinoma 71 7.062
251
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 7.029
252
c LKM061 Leukemia, Acute Myeloid 83 7.019
253
KRT019 Keratitis, Hereditary 66 7.013
254
STM007 Stomatitis 54 7.003
255
ILS001 Ileus 50 6.986
256
HVY002 Heavy Metal Poisoning 22 6.960
257
LPP008 Lipoprotein Quantitative Trait Locus 65 6.959
258
P SNS001 Sensorineural Hearing Loss 59 6.946
259
HGH043 High Grade Glioma 45 6.901
260
IMP005 Impotence 52 6.867
261
INS024 Insulin-Like Growth Factor I 78 6.856
262
P CRN300 Coronary Heart Disease 1 73 6.841
263
P THL005 Thalassemia 56 6.828
264
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 6.819
265
P VSC011 Vasculitis 61 6.812
266
OCL006 Ocular Hypertension 53 6.795
267
PLY012 Polyhydramnios 46 6.790
268
P CLR023 Colorectal Cancer 100 6.765
269
THY029 Thyroid Carcinoma 51 6.748
270
P ALC033 Alcohol Use Disorder 61 6.742
271
LYS002 Lysosomal Storage Disease 51 6.730
272
c PCH010 Pachyonychia Congenita 3 43 6.727
273
P BRS044 Breast Adenocarcinoma 58 6.703
274
P HYP076 Hyperthyroidism 53 6.693
275
P DBT009 Diabetes Mellitus 67 6.676
276
c SCN007 Secondary Hyperparathyroidism 51 6.661
277
HYP014 Hyperuricemia 51 6.656
278
P PLY019 Polyneuropathy 52 6.629
279
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 6.605
280
ADN011 Adenoid Cystic Carcinoma 68 6.599
282
c PRM005 Primary Hyperparathyroidism 59 6.584
283
HMP009 Haemophilus Influenzae 41 6.573
284
ART140 Arteries, Anomalies of 53 6.571
285
P DDN001 Duodenal Ulcer 53 6.541
286
c MCR115 Microvascular Complications of Diabetes 5 65 6.524
287
c ATS007 Autism Spectrum Disorder 72 6.495
288
P ECL001 Eclampsia 52 6.492
289
P MLG056 Malignant Hyperthermia 66 6.481
290
P ART022 Arthritis 71 6.473
291
HYP060 Hyperinsulinism 54 6.461
292
P RTN016 Retinal Degeneration 52 6.434
293
PLG002 Plague 58 6.384
294
OST011 Osteomalacia 52 6.365
295
P CYS018 Cystitis 59 6.322
296
CHL068 Cholestasis 61 6.321
297
P SYS005 Systemic Scleroderma 74 6.317
298
MLR004 Malaria 80 6.307
299
c DLT002 Dilated Cardiomyopathy 78 6.269
300
P INT068 Intestinal Disease 53 6.263
301
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 6.262
302
DYS073 Dysphagia 53 6.251
303
ALL014 Allergic Encephalomyelitis 34 6.245
304
ESP021 Esophageal Cancer 83 6.244
305
c BRT024 Bartter Syndrome Type 4 25 6.207
306
DBT084 Diabetes Mellitus, Ketosis-Prone 60 6.202
307
MNN043 Meningioma, Familial 79 6.193
308
SCR001 Secretory Meningioma 40 6.193
309
LYM002 Lymphoplasmacyte-Rich Meningioma 35 6.193
310
SPN021 Spinal Meningioma 50 6.193
311
CRH001 Crohn's Disease 80 6.185
312
c HPT003 Hepatitis a 63 6.153
313
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 6.128
314
ACT098 Acute Erythroid Leukemia 55 6.118
315
P TRC031 Trichorhinophalangeal Syndrome 38 6.110
316
MNT002 Mental Depression 57 6.099
317
PNC129 Pancreatic Adenocarcinoma 65 6.099
318
HYP017 Hypophosphatemia 49 6.083
319
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 45 6.083
320
P SCK005 Sickle Cell Disease 56 6.077
321
MSC157 Muscular Dystrophy, Duchenne Type 79 6.062
322
P FBR031 Febrile Seizures 52 6.060
323
SFT003 Soft Tissue Sarcoma 57 6.047
324
c BRT042 Bartter Syndrome, Type 3 46 6.029
325
P PRN023 Prion Disease 60 6.026
326
ALL006 Allergic Asthma 56 6.024
327
GST023 Gastric Ulcer 52 6.001
328
c SHR030 Short Qt Syndrome 44 5.974
329
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 5.973
330
DSS032 Disease by Infectious Agent 55 5.971
331
MST005 Mastitis 53 5.968
332
NRG002 Neurogenic Bladder 55 5.966
333
P RCT021 Rectum Cancer 54 5.959
334
P PNM007 Pneumonia 67 5.955
335
SPS057 Spasticity 42 5.950
336
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 5.939
337
P NPH012 Nephrotic Syndrome 60 5.921
338
ORL011 Oral Cancer 60 5.918
339
ORL015 Oral Squamous Cell Carcinoma 43 5.913
340
P BLD134 Bladder Cancer 79 5.911
341
MTH071 Methane Production 25 5.890
342
PTT037 Pituitary Tumors 44 5.888
343
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.882
344
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.882
345
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.882
346
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 5.882
347
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 5.882
348
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.882
349
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 5.882
350
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.882
351
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 5.882
352
P CND004 Candidiasis 58 5.877
353
c GLL024 Gallbladder Disease 1 52 5.871
354
IMM167 Immune Deficiency Disease 78 5.868
355
GST092 Gastroesophageal Reflux 61 5.858
356
P HDC001 Headache 57 5.853
357
TRY001 Trypanosomiasis 50 5.824
358
DPR016 Depression 65 5.776
359
DMP001 Dumping Syndrome 43 5.749
360
P HYP097 Hyperekplexia 62 5.744
361
CLN015 Colon Adenocarcinoma 65 5.742
362
ATR057 Atrioventricular Block 54 5.742
363
STN013 Stenotrophomonas Maltophilia Infection 26 5.723
364
NRT004 Neuritis 53 5.706
365
c FML191 Familial Long Qt Syndrome 55 5.697
366
P MYC008 Myocarditis 59 5.683
367
ANG054 Angina Pectoris 66 5.675
368
c HPT015 Hepatitis D 49 5.674
369
TLN003 Telangiectasis 51 5.670
370
VGN023 Vaginitis 56 5.666
371
PHN003 Phenylketonuria 76 5.661
372
MYL069 Myeloma, Multiple 77 5.660
373
GT001 Gout 64 5.655
374
PND002 Pendred Syndrome 57 5.643
375
RNL114 Renal Cell Carcinoma, Nonpapillary 80 5.639
376
CHD004 Chudley-Mccullough Syndrome 48 5.635
377
PST011 Pustulosis of Palm and Sole 52 5.629
378
P MYL006 Myeloid Leukemia 61 5.609
379
P ENC004 Encephalitis 61 5.602
380
CHL123 Chlamydia 58 5.601
381
DYS015 Dysentery 50 5.581
382
HYP052 Hyperkalemic Periodic Paralysis 63 5.547
383
OST003 Osteonecrosis 61 5.524
384
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 5.502
385
IRN001 Iron Deficiency Anemia 58 5.493
386
CRB039 Cerebrovascular Disease 66 5.483
387
INS001 Insulinoma 59 5.482
388
P ALP008 Alopecia 54 5.480
389
BCT002 Bacterial Vaginosis 53 5.472
390
P MLT020 Multiple Sclerosis 79 5.469
391
P HYP750 Hypertriglyceridemia, Familial 62 5.461
392
DBT010 Diabetic Neuropathy 54 5.460
393
HND015 Hand Skill, Relative 30 5.456
394
GST050 Gastrointestinal System Disease 55 5.443
395
P MJR001 Major Depressive Disorder 68 5.435
396
P PSR002 Psoriasis 63 5.434
397
SBC016 Subacute Delirium 43 5.414
398
c PLM164 Pulmonary Hypertension, Primary, 1 76 5.410
399
P HML002 Hemolytic Anemia 62 5.403
400
P LKD001 Leukodystrophy 59 5.394
401
P MNN013 Meningitis 65 5.394
402
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 5.393
403
ART016 Aortic Aneurysm 68 5.385
404
MSC007 Muscle Hypertrophy 64 5.384
405
CRT015 Carotid Artery Occlusion 45 5.380
406
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 5.370
407
P SCL018 Scoliosis 57 5.337
408
ACQ007 Acquired Immunodeficiency Syndrome 59 5.324
409
P ATS364 Autism 69 5.304
410
PLM001 Pulmonary Tuberculosis 69 5.296
411
c TYP008 Type 1 Diabetes Mellitus 70 5.253
412
ACT003 Acute Kidney Tubular Necrosis 46 5.242
413
OST017 Osteomyelitis 63 5.234
414
LPD008 Lipid Metabolism Disorder 62 5.229
415
P DMN002 Dementia 66 5.220
416
P RTN018 Retinal Disease 53 5.219
417
P PRP029 Porphyria 60 5.195
418
NWC001 Newcastle Disease 47 5.193
419
MTH009 Mouth Disease 57 5.184
420
P EXN002 Exanthem 58 5.166
421
P ART023 Arthropathy 61 5.163
422
MST021 Meester-Loeys Syndrome 42 5.163
423
P LKM002 Leukemia 67 5.160
424
PRT013 Portal Hypertension 59 5.155
425
AMN003 Amnestic Disorder 54 5.151
426
OTT002 Otitis Media 71 5.144
427
SCK003 Sickle Cell Anemia 74 5.143
428
PNC041 Pancreatic Ductal Adenocarcinoma 51 5.132
429
c ACT134 Acute Liver Failure 59 5.128
430
c HPT016 Hepatitis B 62 5.123
431
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 5.114
432
P KDN017 Kidney Cancer 61 5.084
433
SCR011 Scrapie 39 5.050
434
c GLC092 Glaucoma, Primary Open Angle 62 5.042
435
FBR047 Fibromyalgia 58 5.034
436
ANX010 Anxiety 70 5.027
437
MCN017 Meconium Ileus 53 5.010
438
P SPP010 Suppressor of Tumorigenicity 3 51 4.997
439
DMY004 Demyelinating Disease 50 4.991
440
P MSC003 Muscular Atrophy 52 4.989
441
P EPL140 Epilepsy, Idiopathic Generalized 62 4.988
442
PPL022 Papilloma 53 4.983
443
PTH003 Pathologic Nystagmus 52 4.970
444
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 4.970
445
SDD001 Sudden Infant Death Syndrome 60 4.951
446
P ACN011 Acne 57 4.945
447
P INT143 Interstitial Cystitis 60 4.940
448
P PYL005 Pyelonephritis 57 4.938
449
P MVM001 Movement Disease 61 4.938
450
P BNG032 Benign Mesothelioma 53 4.937
451
CTN007 Cutaneous Leishmaniasis 62 4.933
452
MNK001 Menkes Disease 64 4.929
453
SQM002 Squamous Cell Papilloma 46 4.929
454
YLL002 Yellow Fever 61 4.918
455
P ART021 Arteriosclerosis 54 4.917
456
CHR100 Chronic Ulcer of Skin 57 4.914
457
P FML023 Familial Hemiplegic Migraine 53 4.900
458
HDN002 Head Injury 44 4.893
459
RYN005 Raynaud Phenomenon 45 4.882
460
PRS045 Prostatic Hypertrophy 53 4.879
461
HYP267 Hyperchlorhidrosis, Isolated 24 4.878
462
P FML187 Familial Hypertension 34 4.874
463
P HYD006 Hydrocephalus 61 4.868
464
PRM057 Paramyotonia Congenita of Von Eulenburg 59 4.863
465
KRT006 Keratoconjunctivitis 53 4.862
466
ANR040 Aneurysm 61 4.834
467
P ESP024 Esophagitis 60 4.831
468
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 4.828
469
INT075 Intracranial Hypertension 53 4.801
470
P THR014 Thrombocytopenia 66 4.792
471
CVD001 Covid-19 57 4.790
472
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 4.781
473
SCH014 Schistosomiasis 56 4.781
474
END057 Endometrial Cancer 72 4.775
475
P HYP265 Hypotonia 42 4.774
476
P RHB003 Rhabdomyosarcoma 66 4.762
477
CHG001 Chagas Disease 66 4.761
478
AVN001 Avian Influenza 61 4.756
479
MTL005 Metal Allergy 40 4.744
480
SPL018 Splenomegaly 49 4.733
481
P CNJ013 Conjunctivitis 66 4.731
482
c PNS012 Paine Syndrome 60 4.712
483
ERL001 Early Myoclonic Encephalopathy 62 4.706
484
DRY001 Dry Eye Syndrome 50 4.693
485
DNT001 Dental Fluorosis 43 4.691
486
P MYP006 Myopia 56 4.687
487
NRL016 Neural Tube Defects 81 4.682
488
VLV047 Volvulus of Midgut 52 4.681
489
P RHM011 Rheumatoid Arthritis 82 4.657
490
CHL065 Cholangiocarcinoma 58 4.638
491
INT079 Intrahepatic Cholangiocarcinoma 51 4.638
492
P TRN020 Turner Syndrome 67 4.636
493
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 4.619
494
P OPT009 Optic Neuritis 57 4.613
495
P HYP061 Hypertrophic Cardiomyopathy 69 4.598
496
P PRD017 Periodic Paralyses 24 4.598
497
P URT039 Urticaria 58 4.597
498
c RTN047 Retinitis Pigmentosa 18 46 4.580
499
BRN002 Bronchiolitis 57 4.564
500
P INS002 in Situ Carcinoma 53 4.560
501
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 4.554
502
GLC003 Glucose Intolerance 54 4.545
503
P CRN026 Corneal Edema 42 4.529
504
ENT011 Enterocolitis 55 4.523
505
BNG077 Benign Idiopathic Neonatal Seizures 23 4.522
506
c INH020 Inherited Metabolic Disorder 48 4.520
507
c LNG047 Long Qt Syndrome 2 59 4.510
508
P DYS154 Dystonia 64 4.493
509
P DNG005 Dengue Virus 56 4.492
510
TRG002 Trigeminal Neuralgia 61 4.488
511
c MCL013 Mucolipidosis Iv 65 4.485
512
c PRD040 Periodontitis, Chronic 52 4.474
513
P RTN024 Retinoblastoma 73 4.466
514
P LKM062 Leukemia, Acute Lymphoblastic 69 4.460
515
NRR001 Neuroretinitis 42 4.456
516
RTN023 Retinitis 46 4.456
517
CMM005 Common Cold 56 4.456
518
P END044 Endometriosis 62 4.453
519
CHR178 Chromosomal Triplication 34 4.438
520
AZS001 Azoospermia 45 4.432
521
P RTN008 Retinitis Pigmentosa 80 4.423
522
CND006 Candida Glabrata 30 4.422
523
P CLC063 Celiac Disease 1 66 4.414
524
NRM005 Neuromuscular Disease 63 4.400
525
MSL001 Measles 61 4.399
526
P HYP024 Hypoparathyroidism 55 4.392
527
P SLP006 Sleep Apnea 69 4.373
528
OCC016 Occupational Asthma 33 4.355
529
URN010 Urinary Tract Obstruction 55 4.349
530
ADG002 Audiogenic Seizures 25 4.344
531
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 4.322
532
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 4.322
533
P CRD246 Cardiovascular System Disease 56 4.322
534
P ART005 Arteriovenous Malformation 65 4.318
535
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 4.312
536
P ATX030 Ataxia-Telangiectasia 80 4.301
537
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 4.293
538
PLM031 Poliomyelitis 63 4.259
539
IRR003 Irritant Dermatitis 47 4.257
540
ADL002 Adult Syndrome 70 4.246
541
PRS063 Paresthesia 39 4.215
542
PRS021 Prostatic Adenoma 43 4.215
543
P CYS039 Cystic Kidney Disease 53 4.215
544
PHR003 Pharyngitis 58 4.214
545
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 4.213
546
P HYP733 Hypercalciuria, Absorptive, 2 45 4.206
547
KRT001 Keratoconjunctivitis Sicca 50 4.205
548
EXR010 Exercise-Induced Bronchoconstriction 34 4.199
549
INT066 Interstitial Lung Disease 60 4.195
550
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 4.194
551
P MJR007 Major Affective Disorder 1 42 4.186
552
SLP001 Sleeping Sickness 56 4.185
553
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 4.175
554
WLS001 Wilson Disease 70 4.160
555
P SCK002 Sick Sinus Syndrome 55 4.157
556
P LCH002 Lichen Planus 54 4.157
557
GST040 Gastric Adenocarcinoma 67 4.149
558
c SCL052 Scleroderma, Familial Progressive 61 4.149
559
KRT009 Keratosis 53 4.141
560
VRC005 Varicose Veins 60 4.140
561
OST062 Osteoarthritis with Mild Chondrodysplasia 47 4.140
562
BCK006 Back Pain 47 4.137
563
PRR019 Perioral Myoclonia with Absences 27 4.129
564
P CHR012 Chronic Granulomatous Disease 69 4.116
565
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 4.112
566
CLC006 Calcinosis 47 4.105
567
P FNC004 Fanconi Syndrome 60 4.099
568
c VRL010 Viral Hepatitis 53 4.094
569
RBS001 Rabies 58 4.091
570
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 4.077
571
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 4.077
572
P MCL001 Mucolipidosis 49 4.071
573
P SLP005 Sleep Disorder 61 4.059
574
PRS129 Prostatic Hyperplasia, Benign 49 4.057
575
P CNG001 Congenital Myasthenic Syndrome 68 4.056
576
PMP014 Pemphigoid 51 4.055
577
URT010 Ureteral Obstruction 45 4.040
578
P RBL001 Rubella 58 4.031
579
c BTT014 Beta-Thalassemia 72 4.022
580
HMG005 Hemoglobinopathy 56 4.017
581
CRB037 Cerebral Palsy 67 4.015
582
P LPS004 Lupus Erythematosus 61 4.003
583
P NTR004 Neutropenia 63 4.001
584
BCT004 Bacteriuria 47 4.000
585
SNS003 Sensory Peripheral Neuropathy 52 3.999
586
P RRT020 Rare Tumor 39 3.987
587
P MLN069 Melanoma, Uveal 61 3.981
588
SKN019 Skin Melanoma 71 3.979
589
P EPL198 Epilepsy, Myoclonic Juvenile 61 3.976
590
END040 Endogenous Depression 55 3.976
591
RTN017 Retinal Detachment 60 3.959
592
c HMC039 Hemochromatosis, Type 1 73 3.949
593
LYM133 Lymphoma, Hodgkin, Classic 74 3.945
594
LST001 Listeriosis 59 3.942
595
ATN005 Autonomic Dysfunction 46 3.937
596
AMN006 Aminoaciduria 37 3.936
597
P FRG001 Fragile X Syndrome 70 3.930
598
PLM033 Pulmonary Embolism 58 3.928
599
c THY107 Thymoma, Familial 42 3.924
600
P THY023 Thymoma 64 3.924
601
GRN017 Granulocytopenia 42 3.915
602
HMC014 Homocysteinemia 52 3.914
603
PRP027 Peripheral Vascular Disease 71 3.905
604
P THY032 Thyroiditis 57 3.897
605
LTH043 Lithium Transport 17 3.891
606
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.886
607
RHB024 Rhabdomyosarcoma 2 67 3.885
608
P VTL001 Vitelliform Macular Dystrophy 46 3.882
609
c GRV008 Graves Disease 1 54 3.882
610
CRB090 Cerebral Hypoxia 42 3.878
611
IGR001 Ige Responsiveness, Atopic 59 3.867
612
ECT026 Ectopic Pregnancy 48 3.866
613
PRP016 Paraplegia 52 3.864
614
P MGR003 Migraine with Aura 52 3.847
615
P CNR004 Cone-Rod Dystrophy 2 74 3.847
616
HLC007 Helicobacter Pylori Infection 67 3.847
617
c PLM128 Pulmonary Hypertension, Primary, 2 28 3.839
618
P CHR071 Charcot-Marie-Tooth Disease 64 3.838
619
BLL006 Bullous Pemphigoid 61 3.832
620
P MTH007 Methemoglobinemia 46 3.822
621
SPN051 Spondylitis 51 3.822
622
INF009 Inflammatory Spondylopathy 30 3.822
623
PRP030 Purpura 54 3.814
624
DGN001 Degenerative Disc Disease 49 3.813
625
PCD001 Pica Disease 38 3.812
626
MNR012 Meniere Disease 56 3.808
627
NND001 Nondystrophic Myotonia 20 3.806
628
NPH018 Nephrogenic Systemic Fibrosis 49 3.804
629
PYL006 Pyloric Stenosis 48 3.785
630
SQM013 Squamous Cell Carcinoma, Head and Neck 73 3.781
631
DST005 Diastrophic Dysplasia 57 3.776
632
P SBS003 Substance Abuse 54 3.774
633
CHR074 Choriocarcinoma 46 3.770
634
c SPN225 Spondyloarthropathy 1 70 3.756
635
PLC002 Plica Syndrome 35 3.749
636
SYN007 Synovitis 55 3.749
637
VSC002 Vascular Dementia 60 3.748
638
RTN003 Retinal Ischemia 49 3.745
639
P ASP006 Aspergillosis 72 3.743
640
c SYS001 Systemic Lupus Erythematosus 87 3.728
641
P MNC007 Monocytic Leukemia 47 3.725
642
c PNC108 Pancreatitis, Hereditary 69 3.716
643
c MYT029 Myotonia Congenita, Autosomal Recessive 40 3.715
644
P GRV001 Graves' Disease 55 3.712
645
IDP073 Idiopathic Hypercalciuria 40 3.711
646
ANR004 Anuria 44 3.711
647
MNG007 Manganese Poisoning 28 3.710
648
P BNC003 Bone Cancer 58 3.703
649
NNL006 Non-Alcoholic Steatohepatitis 54 3.697
650
P SRC025 Sarcoidosis 1 71 3.695
651
P PNC025 Panic Disorder 52 3.679
652
GNT046 Genetic Epilepsy with Febrile Seizures Plus 29 3.672
653
BST008 Bestrophinopathy, Autosomal Recessive 46 3.656
654
CLF027 Cleft Palate, Isolated 64 3.653
655
GSG001 Gas Gangrene 52 3.652
656
P UVT001 Uveitis 57 3.651
657
P HYP098 Hypereosinophilic Syndrome 66 3.649
658
SPP011 Suppression of Tumorigenicity 12 61 3.637
659
FCL014 Focal Epilepsy 53 3.637
660
CLR109 Colorectal Adenocarcinoma 50 3.634
661
HRD218 Hereditary Stomatocytosis 30 3.633
662
P HMP007 Hemophilia 52 3.616
663
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 49 3.604
664
NRT001 Neurotic Disorder 56 3.596
665
P MDL005 Medulloblastoma 75 3.585
666
NTR005 Nutritional Deficiency Disease 61 3.580
667
BRN056 Bronchopulmonary Dysplasia 56 3.580
668
P NGH001 Night Blindness 52 3.577
669
c PSD093 Pseudohypoaldosteronism, Type Iid 32 3.577
670
P CHL066 Cholangitis 52 3.576
671
c HNT011 Huntington Disease-Like 3 34 3.575
672
P SYP003 Syphilis 59 3.570
673
c ACT249 Acute Asthma 40 3.562
674
ONC002 Onchocerciasis 51 3.562
675
P SHR001 Short Bowel Syndrome 53 3.559
676
c DWL002 Dowling-Degos Disease 1 58 3.556
677
CMB007 Combined Immunodeficiency 57 3.548
678
URT049 Urate Oxidase, Pseudogene 24 3.544
679
P ATT013 Attention Deficit-Hyperactivity Disorder 64 3.543
680
DSS009 Disseminated Intravascular Coagulation 57 3.541
681
MYC005 Myocardial Stunning 46 3.541
682
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 3.532
683
c LKM005 Leukemia, T-Cell, Chronic 34 3.532
684
ART002 Arts Syndrome 66 3.522
685
THY128 Thyroid Tumor 35 3.514
686
c PLM121 Pulmonary Hypertension, Primary, 4 28 3.513
687
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 61 3.506
688
PRT058 Pure Autonomic Failure 58 3.506
689
EMB004 Embryonal Carcinoma 56 3.501
690
P THY054 Thyrotoxic Periodic Paralysis 50 3.489
691
P MTR014 Motor Neuron Disease 65 3.488
692
BLD044 Bladder Disease 48 3.481
693
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 57 3.481
694
FLR002 Filariasis 55 3.477
695
CRD137 Cardiogenic Shock 56 3.465
696
P FML011 Familial Adenomatous Polyposis 71 3.461
697
FML036 Familial Periodic Paralysis 43 3.450
698
HNS001 Hansen's Disease 32 3.444
699
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 3.444
700
c HNT004 Huntington Disease-Like 2 52 3.441
701
ANR007 Anorexia Nervosa 60 3.438
702
CHL004 Cholelithiasis 49 3.438
703
MGL009 Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 48 3.436
704
ACT119 Acute Promyelocytic Leukemia 62 3.434
705
BLR008 Bilirubin Metabolic Disorder 57 3.430
706
P MCR010 Microcephaly 60 3.430
707
c MYT027 Myotonia Congenita, Autosomal Dominant 34 3.417
708
P SLM003 Salmonellosis 54 3.413
709
c ACT004 Acute Diarrhea 40 3.408
710
HYD002 Hydronephrosis 58 3.407
711
P HMR005 Hemorrhoid 49 3.400
712
KRT002 Keratomalacia 55 3.397
713
P GCH001 Gaucher's Disease 70 3.394
714
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 3.394
715
CHR073 Choreatic Disease 54 3.394
716
TBR011 Tuberculous Meningitis 48 3.389
717
EPT021 Epithelial Recurrent Erosion Dystrophy 46 3.382
718
CHR066 Chronic Fatigue Syndrome 60 3.378
719
JMP002 Jumping Frenchmen of Maine 21 3.378
720
c BRT052 Bartter Syndrome, Type 1, Antenatal 43 3.369
721
ENT004 Enthesopathy 51 3.368
722
DRV001 Dravet Syndrome 69 3.366
723
WTH001 Withdrawal Disorder 48 3.360
724
GLM044 Glomerular Disease 35 3.352
725
BRC012 Brucellosis 66 3.351
726
P LKM071 Leukemia, Chronic Lymphocytic 75 3.350
727
P OBS001 Obstructive Jaundice 48 3.340
728
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 3.331
729
CRC006 Carcinoid Syndrome 55 3.330
730
P RNL015 Renal Hypertension 45 3.330
731
TRN015 Transient Cerebral Ischemia 63 3.327
732
KRT008 Keratopathy 46 3.323
733
NRM001 Neuromyelitis Optica 61 3.322
734
MST020 Mast Cell Activation Syndrome 28 3.321
735
c PRS136 Prostate Cancer, Hereditary, 6 33 3.307
736
c PRS130 Prostate Cancer, Hereditary, 8 32 3.307
737
CCC002 Coccidiosis 50 3.300
738
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 3.299
739
P PNM006 Pneumoconiosis 55 3.295
740
ANT018 Anthracosis 51 3.295
741
ALB002 Albinism 47 3.290
742
LCH001 Leech Infestation 38 3.286
743
P ANT061 Antenatal Bartter Syndrome 36 3.280
744
P ANR048 Aniridia 1 64 3.268
745
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 3.263
746
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 3.257
747
P NRV007 Nervous System Disease 67 3.253
748
P MTH008 Methylmalonic Acidemia 52 3.253
749
PLY100 Polyploidy 36 3.244
750
P TCD001 Tic Disorder 49 3.223
751
P LPS002 Liposarcoma 64 3.222
752
P CRV039 Cervicitis 52 3.221
753
CNT105 Central Core Disease of Muscle 59 3.208
754
P ACT105 Acute Mountain Sickness 52 3.203
755
P HYP120 Hypoaldosteronism 35 3.202
756
KLB003 Klebsiella Pneumonia 50 3.199
757
P AVS003 Avascular Necrosis 41 3.197
758
CHK001 Chikungunya 60 3.193
759
P LMB006 Limb-Girdle Muscular Dystrophy 52 3.191
760
P SJG008 Sjogren Syndrome 61 3.191
761
PRM236 Primary Biliary Cholangitis 60 3.190
762
LYM143 Lymphoma, Non-Hodgkin, Familial 75 3.168
763
P GRF003 Graft-Versus-Host Disease 71 3.166
764
HRY003 Hairy Cell Leukemia 61 3.157
765
RTR008 Root Resorption 44 3.147
766
c EPS042 Episodic Ataxia, Type 1 58 3.147
767
WST005 West Nile Virus 57 3.136
768
ENM002 Enamel Erosion 25 3.135
769
PNM008 Pneumothorax 54 3.133
770
MCL006 Macular Retinal Edema 57 3.133
771
P PTT006 Pituitary Adenoma 55 3.132
772
TRN018 Transitional Cell Carcinoma 56 3.129
773
MYL020 Myelomeningocele 51 3.119
774
DDN004 Duodenogastric Reflux 31 3.119
775
MCP006 Mucoepidermoid Carcinoma 48 3.110
776
P LPR021 Leprosy 3 71 3.099
777
P RTT002 Rett Syndrome 79 3.092
778
LBR035 Liberfarb Syndrome 27 3.088
779
FDB001 Foodborne Botulism 55 3.088
780
AND005 Androgen Insensitivity Syndrome, Mild 21 3.084
781
DWR001 Dwarfism 44 3.075
782
c BSL007 Basal Cell Carcinoma 68 3.074
783
CRN019 Coronary Artery Vasospasm 47 3.070
784
CRT004 Carotid Artery Thrombosis 39 3.069
785
P SML001 Small Cell Carcinoma 52 3.068
786
SYS071 Systemic Autoimmune Disease 35 3.066
787
P MPL001 Maple Syrup Urine Disease 70 3.066
788
FCS002 Fucosidosis 62 3.064
789
P TBR001 Tuberous Sclerosis 69 3.060
790
MMM001 Mammary Paget's Disease 53 3.060
791
MCR013 Microphthalmia 60 3.058
792
EXT007 Extracutaneous Mastocytoma 38 3.057
793
MST004 Mast Cell Neoplasm 42 3.057
794
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 3.055
795
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 3.052
796
SNT005 Sinoatrial Node Disease 47 3.040
797
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 43 3.036
798
SCT005 Scott Syndrome 50 3.031
799
HMP005 Hemiplegia 54 3.031
800
CYN003 Cyanide Poisoning 22 3.023
801
P RNV001 Renovascular Hypertension 49 3.022
802
VSC003 Visceral Leishmaniasis 55 3.019
803
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.013
804
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 3.008
805
c HMP029 Hemophilia a 68 3.000
806
BRN014 Bronchopneumonia 53 2.998
807
P MCR129 Microvascular Complications of Diabetes 1 68 2.997
808
IDP070 Idiopathic Scoliosis 42 2.996
809
EXC002 Exocrine Pancreatic Insufficiency 42 2.995
810
CRB086 Cerebral Aneurysms 40 2.994
811
c FML001 Familial Atrial Fibrillation 65 2.992
812
ORL005 Oral Candidiasis 56 2.985
813
P MYC033 Myoclonus 47 2.984
814
P FCL005 Focal Segmental Glomerulosclerosis 57 2.980
815
HYP080 Hypogonadism 50 2.977
816
FCT001 Factor Viii Deficiency 60 2.976
818
c SCN036 Secondary Progressive Multiple Sclerosis 55 2.974
819
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 2.971
820
PRP080 Peripheral Artery Disease 54 2.970
821
P HRD011 Hereditary Spherocytosis 64 2.969
822
c MYT020 Myotonic Dystrophy 2 57 2.967
823
P PTN014 Patent Ductus Arteriosus 1 59 2.958
824
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 2.957
825
LMB002 Lambert-Eaton Myasthenic Syndrome 52 2.952
826
P HYP009 Hypertrophic Pyloric Stenosis 41 2.949
827
P JVN007 Juvenile Absence Epilepsy 47 2.948
828
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 2.947
829
ANT039 Antisynthetase Syndrome 55 2.946
830
HRN029 Hearing Loss, Noise-Induced 37 2.946
831
CHL067 Cholecystitis 60 2.942
832
CYN002 Cyanosis, Transient Neonatal 43 2.940
833
BNG006 Benign Familial Neonatal Epilepsy 55 2.939
834
c TBR025 Tuberous Sclerosis 1 84 2.939
835
c MST023 Mesothelioma, Malignant 56 2.937
836
P TXP001 Toxoplasmosis 60 2.937
838
CMP034 Complete Androgen Insensitivity Syndrome 55 2.935
839
CRT072 Creutzfeldt-Jakob Disease 68 2.932
840
FLR001 Filarial Elephantiasis 59 2.931
841
c ACT073 Acute Leukemia 58 2.931
842
LNG031 Lung Benign Neoplasm 51 2.922
843
EXN003 Exencephaly 30 2.920
844
PSY004 Psychotic Disorder 66 2.907
845
ACR007 Acromegaly 70 2.904
846
ANH002 Anhidrosis 46 2.903
847
P KRT007 Keratoconus 50 2.902
848
c MLG084 Malignant Fibrous Histiocytoma 62 2.902
849
P LYM118 Lymphoma 67 2.900
850
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 2.893
851
P LRY044 Larynx Cancer 54 2.891
852
CNN005 Connective Tissue Disease 67 2.886
853
c BCT007 Bacterial Meningitis 55 2.878
854
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.876
855
MNN009 Meningoencephalitis 48 2.866
856
P EPD016 Epidermolysis Bullosa 53 2.866
857
MYT030 Myotonia, Potassium-Aggravated 46 2.862
858
ESP023 Esophageal Disease 52 2.862
859
c HPT007 Hepatitis E 51 2.860
860
PRT029 Parathyroid Adenoma 51 2.860
861
P LTH003 Lethal Congenital Contracture Syndrome 41 2.856
862
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 2.855
863
RNL077 Renal Fibrosis 46 2.854
864
ANP005 Anaplastic Astrocytoma 57 2.851
865
P CRN025 Corneal Dystrophy 49 2.850
866
P PRS038 Personality Disorder 65 2.847
867
FML159 Familial Periodic Paralyses 16 2.844
868
P LDD007 Liddle Syndrome 1 57 2.843
869
P HMN010 Hemangioma 62 2.841
870
CYS013 Cystinuria 66 2.836
871
OPD006 Opioid Addiction 48 2.817
872
P FBR003 Fibrous Histiocytoma 43 2.809
873
P APL001 Aplastic Anemia 73 2.808
875
NVS001 Neovascular Glaucoma 52 2.807
876
VGN019 Vaginal Discharge 47 2.806
877
THY030 Thyroid Gland Disease 50 2.800
878
CHP002 Chops Syndrome 47 2.800
879
PRM020 Premenstrual Tension 39 2.798
880
P PTS002 Ptosis 52 2.783
881
BRR014 Barrett Esophagus 66 2.779
882
FDL002 Food Allergy 47 2.778
883
RTC003 Root Caries 32 2.776
884
CCN002 Cocaine Abuse 49 2.769
885
RTN020 Retinal Vascular Disease 46 2.769
886
MYL009 Myelodysplastic Syndrome 67 2.767
887
P SLV026 Salivary Gland Carcinoma 58 2.758
888
CHR576 Chronic Beryllium Disease 42 2.757
889
P BRY005 Beryllium Disease 39 2.757
890
c SVR005 Severe Pre-Eclampsia 50 2.757
891
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 2.754
892
HRP004 Herpes Zoster 61 2.747
893
INT067 Interstitial Nephritis 46 2.745
894
P NJM001 Nijmegen Breakage Syndrome 76 2.740
895
GNG003 Gingival Recession 49 2.740
896
ZLL002 Zollinger-Ellison Syndrome 55 2.737
897
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 2.729
898
P SDR002 Siderosis 43 2.728
899
P VTR007 Vitreoretinopathy 46 2.725
900
P GLL018 Gallbladder Cancer 53 2.720
901
TYP007 Typhoid Fever 64 2.719
902
P RNL115 Renal Tubular Acidosis, Proximal 32 2.718
903
HYP264 Hypertonia 36 2.709
904
CRY003 Cryptosporidiosis 56 2.708
905
FNG016 Fungal Keratitis 39 2.704
906
P NRF002 Neurofibromatosis 57 2.703
907
PRN019 Perinatal Necrotizing Enterocolitis 60 2.700
908
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 2.696
909
P MYG005 Myoglobinuria 40 2.696
910
HMN016 Hemangioendothelioma 34 2.692
911
c CHR711 Chronic Asthma 41 2.692
912
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 2.690
913
P PLY018 Polycythemia 56 2.687
914
XRD010 Xeroderma Pigmentosum, Variant Type 73 2.685
915
MTN003 Motion Sickness 51 2.681
916
GST019 Gastrointestinal Stromal Tumor 78 2.675
917
PLC008 Placenta Disease 49 2.667
918
P GLY013 Glycogen Storage Disease 60 2.660
919
P PRM002 Primary Hyperoxaluria 65 2.659
920
P CHN059 Chondrocalcinosis 52 2.656
921
P VNS003 Venous Insufficiency 55 2.646
922
c HRD219 Hereditary Distal Renal Tubular Acidosis 25 2.645
923
P HRD012 Hereditary Elliptocytosis 55 2.643
924
ANP008 Anaplastic Oligoastrocytoma 29 2.642
925
c EXD008 Exudative Vitreoretinopathy 1 71 2.639
926
c OPT053 Optic Atrophy 1 62 2.636
927
BRK010 Burkitt Lymphoma 66 2.636
928
JPN002 Japanese Encephalitis 61 2.636
929
c LKM063 Leukemia, Chronic Myeloid 71 2.630
930
MCL027 Macular Dystrophy, Dominant Cystoid 51 2.628
931
DSS010 Dissociative Disorder 39 2.626
932
c EPS035 Episodic Ataxia, Type 2 63 2.624
933
NRM009 Normokalemic Periodic Paralysis 28 2.622
934
c THR092 Thrombophilia Due to Thrombin Defect 74 2.616
935
APP008 Appendicitis 62 2.614
936
PRX035 Paroxysmal Dyskinesia 30 2.613
937
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 2.608
938
CRV038 Cervical Squamous Cell Carcinoma 58 2.606
939
c MYT021 Myotonic Dystrophy 1 68 2.597
940
c ATM045 Autoimmune Glomerulonephritis 35 2.597
941
KLD004 Keloid Disorder 39 2.594
942
OSM001 Osmotic Diarrhea 28 2.592
943
c ELL005 Elliptocytosis 2 37 2.590
944
c ELL006 Elliptocytosis 3 34 2.590
945
c ATM011 Autoimmune Hepatitis 63 2.590
946
WLL004 Wallerian Degeneration