Search results for sodium

3333 hits were found for sodium

# Family MCID Name MIFTS Score
1
DRR017 Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies 33 9.096
2
DRR013 Diarrhea 8, Secretory Sodium, Congenital 34 6.116
3
SDM005 Sodium Serum Level Quantitative Trait Locus 1 10 4.541
4
OVR093 Overhydrated Hereditary Stomatocytosis 43 4.080
5
MYT030 Myotonia, Potassium-Aggravated 45 3.585
7
SDM004 Sodium-Potassium-Atpase Activity of Red Cell 7 2.892
8
SDM006 Sodium Aurothiomalate Allergy 5 2.887
9
HYP052 Hyperkalemic Periodic Paralysis 61 2.217
10
SYN164 Syndromic Congenital Sodium Diarrhea 8 2.053
11
P NRL027 Neurological Muscular Channelopathy Due to a Genetic Sodium Channel Defect 3 2.048
12
c NRL035 Neurological Channelopathy of the Central Nervous System Due to a Genetic Sodium Channel Defect 2 2.048
13
c HYP595 Hypertension, Essential 84 0.403
14
CLT003 Colitis 62 0.355
15
P KDN018 Kidney Disease 72 0.321
16
CNG034 Congestive Heart Failure 69 0.251
17
c CHR684 Chronic Kidney Disease 70 0.243
18
ULC004 Ulcerative Colitis 73 0.232
19
P HRT032 Heart Disease 75 0.219
20
HYP005 Hypokalemia 55 0.219
21
48X005 48,xyyy 39 0.218
22
OST012 Osteoarthritis 78 0.217
23
MTB004 Metabolic Acidosis 50 0.214
24
P INF037 Inflammatory Bowel Disease 54 0.209
25
LVR012 Liver Cirrhosis 62 0.205
26
ADL002 Adult Syndrome 70 0.188
27
P DRR001 Diarrhea 55 0.185
28
P NRB001 Neuroblastoma 72 0.184
29
ALL026 Allergic Hypersensitivity Disease 62 0.183
30
P SZR006 Seizure Disorder 56 0.182
31
HYP056 Hypoglycemia 66 0.180
32
c ACT071 Acute Kidney Failure 60 0.180
33
P OST002 Osteoporosis 74 0.178
34
CYS001 Cystic Fibrosis 81 0.178
35
c MGR028 Migraine with or Without Aura 1 67 0.178
36
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.175
37
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.175
38
END086 End Stage Renal Disease 51 0.167
39
VSL002 Visual Epilepsy 59 0.166
40
DRM006 Dermatitis 61 0.166
41
THY029 Thyroid Carcinoma 59 0.166
42
LSH001 Leishmaniasis 63 0.165
43
ISC004 Ischemia 58 0.165
44
P KLZ004 Kala-Azar 1 41 0.165
45
HYP066 Hyperglycemia 61 0.164
46
DNT012 Dental Caries 53 0.162
47
PNG002 Pain Agnosia 51 0.159
48
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.159
49
c PNS012 Paine Syndrome 61 0.158
50
P EPL164 Epilepsy 71 0.154
51
P LVR013 Liver Disease 68 0.154
52
P CTR002 Cataract 60 0.152
53
c MCR120 Microvascular Complications of Diabetes 7 47 0.152
54
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.152
55
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.151
56
P HYP086 Hypothyroidism 69 0.151
57
c MCR113 Microvascular Complications of Diabetes 3 52 0.149
58
P CLR023 Colorectal Cancer 99 0.149
59
AST005 Asthma 76 0.148
60
P BRG001 Brugada Syndrome 71 0.148
61
c MCR130 Microvascular Complications of Diabetes 6 41 0.148
62
c MCR133 Microvascular Complications of Diabetes 4 41 0.148
63
P BPL003 Bipolar Disorder 56 0.146
64
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.146
65
c MJR024 Major Affective Disorder 9 41 0.145
66
c MJR022 Major Affective Disorder 8 38 0.145
67
P PRD021 Periodic Paralysis 45 0.143
68
HRW001 Hair Whorl 36 0.143
69
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.142
70
c THR092 Thrombophilia Due to Thrombin Defect 73 0.141
71
P PLM037 Pulmonary Hypertension 67 0.140
72
CNT047 Contact Dermatitis 58 0.140
73
P LNG028 Long Qt Syndrome 66 0.139
74
P TRN020 Turner Syndrome 67 0.138
75
P GLM045 Glioma 63 0.138
76
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.138
77
GLL048 Glial Tumor 45 0.138
78
P RHN004 Rhinitis 57 0.137
79
P DBT009 Diabetes Mellitus 64 0.136
80
P ADN016 Adenocarcinoma 64 0.136
81
MYT011 Myotonia 34 0.136
82
P MYC007 Myocardial Infarction 70 0.135
83
P CRD119 Cardiac Arrest 67 0.135
84
P NPH012 Nephrotic Syndrome 60 0.133
85
P HDC001 Headache 57 0.133
86
HYP266 Hypoxia 57 0.133
87
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.132
88
PLM010 Pulmonary Edema 54 0.131
89
P NRC002 Narcolepsy 52 0.131
90
P CHR345 Chronic Pain 44 0.130
91
P VSC007 Vascular Disease 63 0.129
92
P ENC018 Encephalopathy 61 0.129
93
c RHB024 Rhabdomyosarcoma 2 67 0.128
94
DWN001 Down Syndrome 70 0.126
95
THR024 Thrombosis 57 0.126
96
P NRP001 Neuropathy 56 0.125
97
P CRD246 Cardiovascular System Disease 57 0.124
98
ALL003 Allergic Rhinitis 67 0.123
99
CNS004 Constipation 58 0.123
100
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.123
101
P CNJ013 Conjunctivitis 65 0.121
102
HLX001 Helix Syndrome 47 0.121
103
CLC001 Calciphylaxis 51 0.120
104
BNR002 Bone Resorption Disease 48 0.119
105
OCL069 Ocular Motor Apraxia 51 0.119
106
STR067 Stroke, Ischemic 81 0.118
107
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.118
108
c ACT027 Acute Pancreatitis 60 0.118
109
P DBT005 Diabetes Insipidus 55 0.118
110
ATX019 Ataxia with Vitamin E Deficiency 42 0.117
111
DFC004 Deficiency Anemia 70 0.116
112
c ACT068 Acute Cystitis 63 0.116
113
ADN018 Adenoma 59 0.116
114
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.116
115
P THR014 Thrombocytopenia 67 0.115
116
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.114
117
GST092 Gastroesophageal Reflux 67 0.114
118
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.114
120
CRB039 Cerebrovascular Disease 67 0.113
121
VSC003 Visceral Leishmaniasis 55 0.113
122
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.113
123
P PRS040 Prostate Cancer 97 0.112
124
LNG099 Lung Disease 60 0.112
125
P RNL015 Renal Hypertension 47 0.112
126
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.112
127
STT001 Status Epilepticus 60 0.111
128
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.110
129
c ACT075 Acute Myocardial Infarction 57 0.110
130
NPH009 Nephrolithiasis 55 0.110
131
PLM033 Pulmonary Embolism 59 0.109
132
P CYS018 Cystitis 59 0.109
133
P EXN002 Exanthem 57 0.109
134
P LKM002 Leukemia 68 0.108
135
GLB015 Glioblastoma Multiforme 75 0.107
136
KRT006 Keratoconjunctivitis 53 0.107
137
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.107
138
HMN044 Human Immunodeficiency Virus Type 1 71 0.107
139
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.107
140
IRN002 Iron Metabolism Disease 57 0.107
141
ALL009 Allergic Conjunctivitis 50 0.107
142
CTN007 Cutaneous Leishmaniasis 62 0.106
143
CHL014 Cholera 59 0.106
144
PRM057 Paramyotonia Congenita of Von Eulenburg 58 0.106
145
P TRM003 Tremor 54 0.106
146
P FBR031 Febrile Seizures 53 0.106
147
BRN071 Brain Injury 49 0.106
148
P NTR004 Neutropenia 63 0.105
149
NTR005 Nutritional Deficiency Disease 62 0.105
150
PRT037 Pertussis 65 0.105
151
TRM010 Traumatic Brain Injury 51 0.105
152
PRT036 Peritonitis 64 0.104
153
P HPT023 Hepatocellular Carcinoma 100 0.103
154
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.103
155
HYP025 Hyperphosphatemia 48 0.103
156
c PRC016 Pre-Eclampsia 63 0.103
157
HYP060 Hyperinsulinism 54 0.103
158
P MCR115 Microvascular Complications of Diabetes 5 66 0.102
159
ACQ007 Acquired Immunodeficiency Syndrome 60 0.102
160
P LCT001 Lactic Acidosis 51 0.102
161
c HYP836 Hypercholesterolemia, Familial, 1 73 0.102
162
P GLM007 Glomerulonephritis 57 0.102
163
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.102
164
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.101
165
P CRN300 Coronary Heart Disease 1 63 0.101
166
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.101
167
CYN003 Cyanide Poisoning 24 0.101
168
P PRD008 Periodontitis 64 0.100
169
ATM095 Autoimmune Disease 62 0.100
170
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.100
171
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.100
172
P LNG032 Lung Cancer 98 0.100
173
P BRS047 Breast Cancer 97 0.100
174
P DRM053 Dermatitis, Atopic 66 0.100
175
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.100
176
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.100
177
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.100
178
DRY001 Dry Eye Syndrome 47 0.100
179
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.100
180
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.100
181
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.100
182
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.100
183
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.100
184
P PSD003 Pseudohypoaldosteronism 44 0.100
185
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.100
186
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.100
187
CYT002 Cytokine Deficiency 42 0.100
188
P GST053 Gastric Cancer 83 0.099
189
CRB004 Cerebral Artery Occlusion 45 0.099
190
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.098
191
RCK004 Rickets 68 0.097
192
IMM167 Immune Deficiency Disease 78 0.097
193
P PNM007 Pneumonia 68 0.097
194
ATH013 Atherosclerosis Susceptibility 65 0.097
195
P INT143 Interstitial Cystitis 61 0.096
196
P PNC044 Pancreatitis 61 0.096
197
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.096
198
IRR003 Irritant Dermatitis 49 0.096
199
EYD002 Eye Disease 58 0.095
200
URM002 Uremia 49 0.095
201
c LNG048 Long Qt Syndrome 3 53 0.095
202
KRT001 Keratoconjunctivitis Sicca 49 0.095
203
GNG013 Gingivitis 59 0.094
204
ANX004 Anoxia 40 0.094
205
P ART022 Arthritis 69 0.093
206
TXC005 Toxic Shock Syndrome 62 0.093
207
VRC005 Varicose Veins 60 0.093
208
c PRS136 Prostate Cancer, Hereditary, 6 33 0.093
209
c PRS130 Prostate Cancer, Hereditary, 8 32 0.093
210
CHL068 Cholestasis 61 0.093
211
FTT001 Fatty Liver Disease 61 0.093
212
SPN186 Spinal Cord Injury 60 0.093
213
BRN004 Brain Edema 56 0.093
214
P ATR011 Atrial Fibrillation 66 0.092
215
P PRP019 Peripheral Nervous System Disease 58 0.092
216
ARG004 Argyria 27 0.092
217
c SYS001 Systemic Lupus Erythematosus 86 0.091
218
P RSP003 Respiratory Failure 74 0.091
219
P MYP004 Myopathy 70 0.091
220
LPP008 Lipoprotein Quantitative Trait Locus 62 0.091
221
P ESP024 Esophagitis 62 0.091
222
CRD223 Cardiac Arrhythmia 60 0.091
223
CRD132 Cardiac Conduction Defect 58 0.091
224
P RHM011 Rheumatoid Arthritis 80 0.090
225
c DBT099 Diabetes Mellitus, Type I 65 0.090
226
P LPS004 Lupus Erythematosus 61 0.090
227
BCT022 Bacterial Infectious Disease 56 0.090
228
P GST044 Gastritis 56 0.090
229
P MYL006 Myeloid Leukemia 60 0.090
230
CHL079 Children's Interstitial Lung Disease 26 0.090
231
P LYM118 Lymphoma 68 0.089
232
MCL006 Macular Retinal Edema 55 0.089
233
SPS057 Spasticity 45 0.089
234
ANG054 Angina Pectoris 66 0.088
235
P SJG008 Sjogren Syndrome 61 0.088
236
P LDD007 Liddle Syndrome 1 59 0.088
237
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.088
238
HYP017 Hypophosphatemia 50 0.088
239
P MJR007 Major Affective Disorder 1 43 0.088
240
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.087
241
P HYP076 Hyperthyroidism 55 0.087
242
P ERY008 Erythromelalgia 47 0.087
243
URL001 Urolithiasis 45 0.087
244
GST023 Gastric Ulcer 53 0.087
245
STM007 Stomatitis 50 0.087
246
PRT013 Portal Hypertension 59 0.086
247
ANX010 Anxiety 73 0.085
248
P MLT020 Multiple Sclerosis 72 0.085
249
P RNV001 Renovascular Hypertension 48 0.085
250
c ATR087 Atrial Standstill 1 75 0.084
251
GT001 Gout 64 0.084
252
KRT009 Keratosis 51 0.084
253
HPT004 Hepatic Coma 45 0.084
254
P PHC003 Pheochromocytoma 71 0.083
255
P BND020 Bone Disease 59 0.083
256
P ECL001 Eclampsia 50 0.083
257
ENT004 Enthesopathy 49 0.083
258
CLC006 Calcinosis 48 0.083
259
ADR040 Adrenal Gland Pheochromocytoma 46 0.083
260
c MLG068 Malignant Glioma 46 0.083
261
P BLD134 Bladder Cancer 79 0.083
262
P MLG056 Malignant Hyperthermia 67 0.083
263
47X002 47,xyy 49 0.083
264
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.082
265
P SLP006 Sleep Apnea 69 0.082
266
DBT010 Diabetic Neuropathy 54 0.082
267
ART140 Arteries, Anomalies of 52 0.082
268
P MTH007 Methemoglobinemia 46 0.082
269
c MJR008 Major Affective Disorder 2 35 0.082
270
c MJR023 Major Affective Disorder 7 33 0.082
271
c MJR003 Major Affective Disorder 6 33 0.082
272
c MJR006 Major Affective Disorder 5 33 0.082
273
c MJR004 Major Affective Disorder 4 28 0.082
274
MYL069 Myeloma, Multiple 85 0.081
275
c LKM061 Leukemia, Acute Myeloid 84 0.081
276
P SCH015 Schizophrenia 74 0.081
277
LYM019 Lymphosarcoma 46 0.081
278
ESP021 Esophageal Cancer 90 0.080
279
P ALZ034 Alzheimer Disease 88 0.080
280
c DLT002 Dilated Cardiomyopathy 79 0.080
281
PRP027 Peripheral Vascular Disease 71 0.080
282
OST159 Osteogenic Sarcoma 66 0.080
283
P PLY014 Polycystic Kidney Disease 62 0.080
284
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.080
285
HPT019 Hepatic Encephalopathy 60 0.080
286
GLS018 Glass Syndrome 57 0.080
287
ALL010 Allergic Contact Dermatitis 56 0.080
288
P SCK005 Sickle Cell Disease 50 0.080
289
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.079
290
GST045 Gastroenteritis 59 0.079
291
PPT005 Peptic Ulcer Disease 59 0.079
292
P BCL017 B-Cell Lymphoma 58 0.079
293
P URT039 Urticaria 58 0.079
294
INT075 Intracranial Hypertension 53 0.079
295
c MCR129 Microvascular Complications of Diabetes 1 66 0.078
296
GTR002 Goiter 53 0.078
297
P PNC025 Panic Disorder 53 0.078
298
P DDN001 Duodenal Ulcer 52 0.078
299
P RNL007 Renal Tubular Acidosis 51 0.078
300
P HYP069 Hyperparathyroidism 63 0.078
301
SKN016 Skin Disease 63 0.078
302
LPD008 Lipid Metabolism Disorder 62 0.078
303
MST005 Mastitis 53 0.078
304
KHN001 Kuhnt-Junius Degeneration 47 0.078
305
P HYP098 Hypereosinophilic Syndrome 67 0.077
306
P HRP006 Herpes Simplex 65 0.077
307
GNT046 Genetic Epilepsy with Febrile Seizures Plus 27 0.077
308
ALC007 Alcohol Dependence 66 0.076
309
c SML038 Small Cell Cancer of the Lung 65 0.076
310
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.076
311
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.076
312
MCS002 Mucositis 56 0.076
313
THY030 Thyroid Gland Disease 52 0.076
314
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.075
315
KRT019 Keratitis, Hereditary 65 0.075
316
DPR016 Depression 63 0.075
317
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.075
318
c FNC043 Fanconi Anemia, Complementation Group E 62 0.074
319
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.074
320
P GRV001 Graves' Disease 55 0.074
321
BRN028 Brain Cancer 74 0.073
322
P MSC005 Muscular Dystrophy 66 0.073
323
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.073
324
ERL001 Early Myoclonic Encephalopathy 62 0.073
325
SCH014 Schistosomiasis 57 0.073
326
AGN016 Aging 56 0.073
327
SPN035 Spindle Cell Sarcoma 53 0.073
328
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.073
329
P DNT007 Dentin Sensitivity 36 0.073
330
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.072
331
P LKM071 Leukemia, Chronic Lymphocytic 79 0.072
332
P MLN008 Melanoma 69 0.072
333
TTN003 Tetanus 65 0.072
334
SRC014 Sarcoma 65 0.072
335
PRT058 Pure Autonomic Failure 59 0.072
336
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.072
337
P PYL005 Pyelonephritis 56 0.072
338
P LTR001 Lateral Sclerosis 54 0.072
339
HYP014 Hyperuricemia 52 0.072
340
PPT001 Peptic Esophagitis 52 0.072
341
HPR003 Heparin-Induced Thrombocytopenia 48 0.072
342
P OVR042 Ovarian Cancer 88 0.071
343
P DYS154 Dystonia 65 0.071
344
ALL006 Allergic Asthma 56 0.071
345
P AST007 Astrocytoma 51 0.071
346
c PRM038 Primary Agammaglobulinemia 44 0.071
347
P PNC035 Pancreatic Cancer 84 0.070
348
SCK003 Sickle Cell Anemia 74 0.070
349
P ADL010 Adult Respiratory Distress Syndrome 65 0.070
350
SQM006 Squamous Cell Carcinoma 60 0.070
351
INT007 Intermediate Coronary Syndrome 55 0.070
352
P ACT008 Actinic Keratosis 53 0.070
353
NPH003 Nephrocalcinosis 51 0.070
354
HDN002 Head Injury 46 0.070
355
MYL009 Myelodysplastic Syndrome 70 0.069
356
BRN024 Bronchitis 68 0.069
357
PSY004 Psychotic Disorder 67 0.069
358
FBR047 Fibromyalgia 58 0.069
359
P RTN016 Retinal Degeneration 53 0.069
360
P TMP001 Temporal Lobe Epilepsy 50 0.069
361
PLM001 Pulmonary Tuberculosis 69 0.068
362
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.068
363
MDD011 Mood Disorder 62 0.068
364
SDD001 Sudden Infant Death Syndrome 61 0.068
365
ANR040 Aneurysm 59 0.068
366
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.068
367
LNG031 Lung Benign Neoplasm 51 0.068
368
SBC016 Subacute Delirium 44 0.068
369
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.068
370
P ATS364 Autism 70 0.067
371
P LKM062 Leukemia, Acute Lymphoblastic 69 0.067
372
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.067
373
P PSR002 Psoriasis 62 0.067
374
NNL006 Non-Alcoholic Steatohepatitis 54 0.067
375
PST011 Pustulosis of Palm and Sole 52 0.067
376
DBT006 Diabetic Macular Edema 48 0.067
377
SYN036 Syncope 45 0.067
378
P FML187 Familial Hypertension 37 0.067
379
P MYC008 Myocarditis 59 0.066
380
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.066
381
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.066
382
ALL014 Allergic Encephalomyelitis 38 0.066
383
PPL052 Papillomatosis, Confluent and Reticulated 33 0.066
384
P GLM040 Glioma Susceptibility 1 81 0.065
385
P HPT021 Hepatitis 67 0.065
386
P CND004 Candidiasis 58 0.065
387
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.065
388
c MCR112 Microvascular Complications of Diabetes 2 41 0.065
389
P LPR021 Leprosy 3 69 0.064
390
P HYP750 Hypertriglyceridemia, Familial 62 0.064
391
NWB001 Newborn Respiratory Distress Syndrome 58 0.064
392
PPL022 Papilloma 54 0.064
393
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.064
394
BCK006 Back Pain 42 0.064
395
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.064
396
HNS001 Hansen's Disease 34 0.064
397
CRH001 Crohn's Disease 74 0.063
398
c HPT016 Hepatitis B 59 0.063
399
MNT002 Mental Depression 58 0.063
400
CYT008 Cytomegalovirus Infection 57 0.063
401
GST050 Gastrointestinal System Disease 56 0.063
402
P ART021 Arteriosclerosis 54 0.063
403
ENT011 Enterocolitis 51 0.063
404
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.063
405
INS024 Insulin-Like Growth Factor I 79 0.062
406
RTN017 Retinal Detachment 61 0.062
407
P SLP005 Sleep Disorder 59 0.062
408
PRX015 Paroxysmal Extreme Pain Disorder 58 0.062
409
P SCK002 Sick Sinus Syndrome 55 0.062
410
FCL014 Focal Epilepsy 54 0.062
411
URC002 Urea Cycle Disorder 51 0.062
412
HYP081 Hypolipoproteinemia 51 0.062
413
SQM002 Squamous Cell Papilloma 46 0.062
414
CVD001 Covid-19 44 0.062
415
P HMN010 Hemangioma 61 0.061
416
P THL005 Thalassemia 60 0.061
417
AYM001 Ayme-Gripp Syndrome 57 0.061
418
SFT003 Soft Tissue Sarcoma 56 0.061
419
AMN003 Amnestic Disorder 54 0.061
420
TND005 Tendinitis 54 0.061
421
PLS009 Plasma Cell Neoplasm 51 0.061
422
P BNG032 Benign Mesothelioma 46 0.061
423
c DRR009 Diarrhea 6 46 0.061
424
GST020 Gastric Antral Vascular Ectasia 41 0.061
425
CRB086 Cerebral Aneurysms 40 0.061
426
LYM133 Lymphoma, Hodgkin, Classic 69 0.060
427
CNN005 Connective Tissue Disease 68 0.060
428
OST017 Osteomyelitis 64 0.060
429
CHR074 Choriocarcinoma 47 0.060
430
RTN023 Retinitis 46 0.060
431
ACT003 Acute Kidney Tubular Necrosis 45 0.060
432
NRR001 Neuroretinitis 42 0.060
433
CYT004 Cytomegalic Inclusion Disease 31 0.060
434
SVR004 Severe Combined Immunodeficiency 73 0.059
435
P CNR004 Cone-Rod Dystrophy 2 73 0.059
436
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.059
437
CLN015 Colon Adenocarcinoma 65 0.059
438
c BRN108 Branchiootic Syndrome 1 62 0.059
439
MSL001 Measles 62 0.059
440
P UVT001 Uveitis 57 0.059
441
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.059
442
FDL002 Food Allergy 51 0.059
443
P FNC004 Fanconi Syndrome 50 0.059
444
ATS010 Autosomal Recessive Disease 48 0.059
445
PLL012 Pollen Allergy 46 0.059
446
CNT025 Central Pontine Myelinolysis 46 0.059
447
PST092 Posttransplant Acute Limbic Encephalitis 29 0.059
448
MSC007 Muscle Hypertrophy 64 0.058
449
ACT119 Acute Promyelocytic Leukemia 63 0.058
450
IRN001 Iron Deficiency Anemia 59 0.058
451
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.058
452
SYN007 Synovitis 54 0.058
453
LYM040 Lymphoblastic Lymphoma 54 0.058
454
MMM001 Mammary Paget's Disease 53 0.058
455
PLP001 Pulpitis 49 0.058
456
c MLG069 Malignant Hypertension 47 0.058
457
MXD026 Mixed Glioma 45 0.058
458
c HYP272 Hypercholesterolemia, Familial, 3 44 0.058
459
IDP033 Idiopathic Edema 44 0.058
460
PLC002 Plica Syndrome 36 0.058
461
ENM002 Enamel Erosion 26 0.058
462
NRL016 Neural Tube Defects 82 0.057
463
P RTN024 Retinoblastoma 73 0.057
464
P ART023 Arthropathy 62 0.057
465
INT002 Intermittent Claudication 61 0.057
466
c SCL052 Scleroderma, Familial Progressive 61 0.057
467
RHM001 Rheumatic Fever 60 0.057
468
IGR001 Ige Responsiveness, Atopic 59 0.057
469
P ALC033 Alcohol Use Disorder 58 0.057
470
GLC003 Glucose Intolerance 54 0.057
471
c FML008 Familial Retinoblastoma 53 0.057
472
IMP005 Impotence 52 0.057
473
HPT014 Hepatorenal Syndrome 50 0.057
474
c BPL002 Bipolar I Disorder 49 0.057
475
c INH020 Inherited Metabolic Disorder 47 0.057
476
P MYC033 Myoclonus 46 0.057
477
P MLG074 Malignant Mesenchymoma 40 0.057
478
P FNC034 Fanconi Renotubular Syndrome 2 40 0.057
479
c NRF023 Neurofibromatosis, Type Ii 80 0.055
480
CNN003 Conn's Syndrome 79 0.055
481
P AMY004 Amyloidosis 70 0.055
482
P FLL037 Follicular Lymphoma 67 0.055
483
APN008 Apnea, Obstructive Sleep 64 0.055
484
c HPT001 Hepatitis C 62 0.055
485
RNL024 Renal Glucosuria 58 0.055
486
P SYP003 Syphilis 58 0.055
487
DSS009 Disseminated Intravascular Coagulation 57 0.055
488
c FML191 Familial Long Qt Syndrome 53 0.055
489
WTH001 Withdrawal Disorder 48 0.055
490
GRN017 Granulocytopenia 44 0.055
491
TND004 Tendinopathy 43 0.055
492
49X006 49, Xxxxy Syndrome 41 0.055
493
OTT002 Otitis Media 72 0.054
494
P SYS005 Systemic Scleroderma 68 0.054
495
SKN019 Skin Melanoma 68 0.054
496
BRK010 Burkitt Lymphoma 67 0.054
497
P NSP012 Nasopharyngeal Carcinoma 66 0.054
498
P MNN013 Meningitis 66 0.054
499
c CNG006 Congenital Hypothyroidism 64 0.054
500
P HML002 Hemolytic Anemia 63 0.054
501
P VSC011 Vasculitis 62 0.054
502
P SNS001 Sensorineural Hearing Loss 60 0.054
503
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.054
504
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 59 0.054
505
BRN002 Bronchiolitis 59 0.054
506
c ACT073 Acute Leukemia 58 0.054
507
BLR008 Bilirubin Metabolic Disorder 57 0.054
508
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.054
509
PRS045 Prostatic Hypertrophy 53 0.054
510
HYP781 Hypoascorbemia 51 0.054
511
CYT005 Cytomegalovirus Retinitis 50 0.054
512
CHD004 Chudley-Mccullough Syndrome 46 0.054
513
IDP073 Idiopathic Hypercalciuria 43 0.054
514
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.054
515
P NRV007 Nervous System Disease 66 0.053
516
GTL001 Gitelman Syndrome 65 0.053
517
c FML001 Familial Atrial Fibrillation 65 0.053
518
P EPL140 Epilepsy, Idiopathic Generalized 62 0.053
519
THY122 Thyroid Gland Cancer 57 0.053
520
c MST023 Mesothelioma, Malignant 57 0.053
521
P ALP008 Alopecia 54 0.053
522
P END047 Endophthalmitis 53 0.053
523
PRP080 Peripheral Artery Disease 53 0.053
524
c GLL024 Gallbladder Disease 1 53 0.053
525
OST011 Osteomalacia 52 0.053
526
DYS015 Dysentery 52 0.053
527
P MSC003 Muscular Atrophy 52 0.053
528
THR016 Thrombophlebitis 51 0.053
529
DYS073 Dysphagia 50 0.053
530
P OTS001 Otosclerosis 49 0.053
531
VRN004 Vernal Keratoconjunctivitis 47 0.053
532
RTR008 Root Resorption 45 0.053
533
c PCH010 Pachyonychia Congenita 3 44 0.053
534
c CHR064 Chronic Monocytic Leukemia 33 0.053
535
MLR004 Malaria 81 0.052
536
P LNG064 Lung Cancer Susceptibility 3 78 0.052
537
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.052
538
P MTR014 Motor Neuron Disease 65 0.052
539
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.052
540
c SVR001 Severe Acute Respiratory Syndrome 62 0.052
541
P DRM010 Dermatomyositis 61 0.052
542
PRS047 Prostatitis 56 0.052
543
P HYP024 Hypoparathyroidism 56 0.052
544
c GRV008 Graves Disease 1 56 0.052
545
ATR057 Atrioventricular Block 55 0.052
546
c FML035 Familial Hyperlipidemia 55 0.052
547
HMP005 Hemiplegia 55 0.052
548
CRT017 Cartilage Disease 54 0.052
549
P RTN018 Retinal Disease 53 0.052
550
TLN003 Telangiectasis 52 0.052
551
PRS021 Prostatic Adenoma 51 0.052
552
SCH012 Schizoaffective Disorder 50 0.052
553
P MYT002 Myotonic Dystrophy 49 0.052
554
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.052
555
PRR019 Perioral Myoclonia with Absences 27 0.052
556
P PRD017 Periodic Paralyses 25 0.052
557
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.050
558
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.050
559
P PRK057 Parkinson Disease, Late-Onset 78 0.050
560
P MDL005 Medulloblastoma 77 0.050
561
CRV035 Cervical Cancer 76 0.050
562
c SPN225 Spondyloarthropathy 1 73 0.050
563
P GRF003 Graft-Versus-Host Disease 72 0.050
564
c LKM063 Leukemia, Chronic Myeloid 72 0.050
565
ACR007 Acromegaly 71 0.050
566
c INF071 Inflammatory Bowel Disease 1 67 0.050
567
P DMN002 Dementia 66 0.050
568
P PLM036 Pulmonary Fibrosis 65 0.050
569
P ART005 Arteriovenous Malformation 65 0.050
570
IRR002 Irritable Bowel Syndrome 65 0.050
571
P MVM001 Movement Disease 63 0.050
572
P KDN017 Kidney Cancer 60 0.050
573
DSS008 Disease of Mental Health 58 0.050
574
P MYT023 Myotonia Congenita 56 0.050
575
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.050
576
P SBS003 Substance Abuse 55 0.050
577
P INT068 Intestinal Disease 53 0.050
578
CHR073 Choreatic Disease 52 0.050
579
ILS001 Ileus 51 0.050
580
INP001 Inappropriate Adh Syndrome 49 0.050
581
c FLL041 Follicular Lymphoma 1 49 0.050
582
P MGR001 Migraine Without Aura 49 0.050
583
MCC002 Mucocutaneous Leishmaniasis 47 0.050
584
KRT002 Keratomalacia 47 0.050
585
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.050
586
P CRN026 Corneal Edema 43 0.050
587
c SYS043 Systemic Lupus Erythematosus 1 38 0.050
588
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.050
589
END057 Endometrial Cancer 74 0.049
590
P HNT016 Huntington Disease 72 0.049
591
CHL065 Cholangiocarcinoma 68 0.049
592
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.049
593
P GLL022 Guillain-Barre Syndrome 59 0.049
594
P INT070 Intestinal Obstruction 58 0.049
595
ERY029 Erythermalgia, Primary 58 0.049
596
CHL067 Cholecystitis 57 0.049
597
BRN056 Bronchopulmonary Dysplasia 57 0.049
598
CMM005 Common Cold 57 0.049
599
P ANG015 Angioedema 57 0.049
600
c ACT134 Acute Liver Failure 56 0.049
601
LMB062 Limb Ischemia 55 0.049
602
URN010 Urinary Tract Obstruction 55 0.049
603
PRP030 Purpura 54 0.049
604
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.049
605
P THY032 Thyroiditis 52 0.049
606
INT079 Intrahepatic Cholangiocarcinoma 51 0.049
607
INT067 Interstitial Nephritis 48 0.049
608
EPC002 Epicondylitis 41 0.049
609
DNT006 Dental Pulp Necrosis 41 0.049
610
PRS063 Paresthesia 41 0.049
611
SCR003 Secretory Diarrhea 37 0.049
612
P HYP120 Hypoaldosteronism 36 0.049
613
c BTT014 Beta-Thalassemia 74 0.048
614
P HYP061 Hypertrophic Cardiomyopathy 70 0.048
615
P MJR001 Major Depressive Disorder 68 0.048
616
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.048
617
BRR014 Barrett Esophagus 65 0.048
618
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.048
619
c HPT003 Hepatitis a 62 0.048
620
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.048
621
P ENC004 Encephalitis 61 0.048
622
HLC007 Helicobacter Pylori Infection 59 0.048
623
P ANP001 Anaplastic Large Cell Lymphoma 58 0.048
624
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.048
625
TNS005 Tonsillitis 57 0.048
626
END040 Endogenous Depression 55 0.048
627
FRZ001 Frozen Shoulder 53 0.048
628
FNG017 Fungal Infectious Disease 53 0.048
629
TXC002 Toxic Encephalopathy 53 0.048
630
DMY004 Demyelinating Disease 52 0.048
631
PTH003 Pathologic Nystagmus 52 0.048
632
P CHL066 Cholangitis 51 0.048
633
VCC001 Vaccinia 49 0.048
634
KRT008 Keratopathy 47 0.048
635
CRD137 Cardiogenic Shock 47 0.048
636
KRT013 Keratolytic Winter Erythema 46 0.048
637
URT010 Ureteral Obstruction 45 0.048
638
CYN002 Cyanosis, Transient Neonatal 45 0.048
639
DST006 Diastolic Heart Failure 45 0.048
640
c MYC068 Myoclonic Epilepsy of Infancy 36 0.048
641
RTC003 Root Caries 33 0.048
642
MTH071 Methane Production 26 0.048
643
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.048
644
MSC157 Muscular Dystrophy, Duchenne Type 72 0.046
645
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.046
646
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.046
647
MNT001 Mantle Cell Lymphoma 69 0.046
648
P OLG002 Oligodendroglioma 67 0.046
649
P SKN015 Skin Carcinoma 66 0.046
650
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.046
651
WST001 West Syndrome 61 0.046
652
HRP004 Herpes Zoster 60 0.046
653
PRN019 Perinatal Necrotizing Enterocolitis 59 0.046
654
c PRM005 Primary Hyperparathyroidism 58 0.046
655
P INF032 Infertility 57 0.046
656
NRT001 Neurotic Disorder 53 0.046
657
P RTN022 Retinal Vein Occlusion 53 0.046
658
PRP016 Paraplegia 52 0.046
659
MRG003 Marginal Zone B-Cell Lymphoma 52 0.046
660
P OVR082 Overgrowth Syndrome 50 0.046
661
SYS003 Systolic Heart Failure 49 0.046
662
PRS129 Prostatic Hyperplasia, Benign 49 0.046
663
BRS064 Bursitis 48 0.046
664
IGG001 Iga Glomerulonephritis 48 0.046
665
RNL077 Renal Fibrosis 47 0.046
666
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.046
667
P HYP265 Hypotonia 43 0.046
668
RDN001 Reading Disorder 40 0.046
669
SCR011 Scrapie 39 0.046
670
FRN014 Fournier Gangrene 37 0.046
671
KPS004 Kaposi Sarcoma 75 0.045
672
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.045
673
c ATS007 Autism Spectrum Disorder 67 0.045
674
P PRS038 Personality Disorder 65 0.045
675
CTR172 Citrullinemia, Classic 64 0.045
676
BLL006 Bullous Pemphigoid 62 0.045
677
TRG002 Trigeminal Neuralgia 60 0.045
678
P CHR285 Chronic Myelomonocytic Leukemia 60 0.045
679
GRD007 Grade Iii Astrocytoma 59 0.045
680
P END033 Endocarditis 57 0.045
681
P PLY011 Polycystic Ovary Syndrome 56 0.045
682
ERY051 Erythroleukemia, Familial 56 0.045
683
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.045
684
ORL005 Oral Candidiasis 56 0.045
685
P PLY019 Polyneuropathy 56 0.045
686
TRD006 Tardive Dyskinesia 54 0.045
687
ACR041 Acromelic Frontonasal Dysostosis 52 0.045
688
P BRT004 Bartter Disease 52 0.045
689
DFF036 Differentiated Thyroid Carcinoma 52 0.045
690
SPN051 Spondylitis 51 0.045
691
P SPP010 Suppressor of Tumorigenicity 3 51 0.045
692
c BRG005 Brugada Syndrome 1 51 0.045
693
NTR046 Neutrophil Migration 50 0.045
694
SNT005 Sinoatrial Node Disease 49 0.045
695
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.045
696
PLS025 Plasmablastic Lymphoma 47 0.045
697
CNT033 Central Nervous System Cancer 47 0.045
698
P SBR004 Seborrheic Dermatitis 45 0.045
699
P BCT020 Bacteremia 2 44 0.045
700
MYF002 Myofascial Pain Syndrome 42 0.045
701
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.045
702
ATM052 Autoimmune Disease 1 37 0.045
703
c LKM005 Leukemia, T-Cell, Chronic 34 0.045
704
INF009 Inflammatory Spondylopathy 31 0.045
705
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.045
706
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.045
707
LPT014 Leptin Deficiency or Dysfunction 74 0.043
708
c MNN043 Meningioma, Familial 74 0.043
709
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.043
710
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.043
711
MNN042 Meningioma, Radiation-Induced 62 0.043
712
P PRP029 Porphyria 62 0.043
713
ARG002 Argininosuccinic Aciduria 61 0.043
714
VRL011 Viral Infectious Disease 61 0.043
715
DPH001 Diphtheria 60 0.043
716
P BRN022 Bronchiectasis 59 0.043
717
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.043
718
SCH003 Schizophreniform Disorder 56 0.043
719
HPT022 Hepatoblastoma 56 0.043
720
P MYP006 Myopia 55 0.043
721
P VNS003 Venous Insufficiency 55 0.043
722
GLS001 Gliosarcoma 54 0.043
723
c PSR017 Psoriasis 2 53 0.043
724
NRT004 Neuritis 52 0.043
725
SPL004 Splenic Marginal Zone Lymphoma 51 0.043
726
SPN021 Spinal Meningioma 50 0.043
727
P OBS001 Obstructive Jaundice 50 0.043
728
MYC005 Myocardial Stunning 46 0.043
729
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.043
730
GNG003 Gingival Recession 44 0.043
731
SCR001 Secretory Meningioma 41 0.043
732
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.043
733
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.043
734
ENT001 Enterocele 39 0.043
735
c CHR682 Chronic Bilirubin Encephalopathy 39 0.043
736
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.043
737
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.043
738
GST040 Gastric Adenocarcinoma 70 0.042
739
CRB037 Cerebral Palsy 69 0.042
740
CRP001 Carpal Tunnel Syndrome 67 0.042
741
P MST009 Mastocytosis 64 0.042
742
P RHB003 Rhabdomyosarcoma 63 0.042
743
TRN015 Transient Cerebral Ischemia 63 0.042
744
HMT002 Hematologic Cancer 62 0.042
745
YLL002 Yellow Fever 61 0.042
746
CHR066 Chronic Fatigue Syndrome 61 0.042
747
INT066 Interstitial Lung Disease 60 0.042
748
ING001 Inguinal Hernia 60 0.042
749
P OPT006 Optic Nerve Disease 60 0.042
750
CHL123 Chlamydia 59 0.042
751
TRN018 Transitional Cell Carcinoma 56 0.042
752
ACT058 Active Peptic Ulcer Disease 55 0.042
753
HRT012 Heart Valve Disease 53 0.042
754
c PRD040 Periodontitis, Chronic 53 0.042
755
c PSR023 Psoriasis 1 52 0.042
756
NRM004 Neuroma 51 0.042
757
c SCN007 Secondary Hyperparathyroidism 51 0.042
758
P OPN001 Open-Angle Glaucoma 49 0.042
759
c HPT015 Hepatitis D 49 0.042
760
ASP007 Aspiration Pneumonia 48 0.042
761
c PSR032 Psoriasis 11 47 0.042
762
ATN005 Autonomic Dysfunction 46 0.042
763
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.042
764
MYX004 Myxedema 43 0.042
765
P CLS010 Cluster Headache 42 0.042
766
c PSR028 Psoriasis 7 42 0.042
767
c PSR018 Psoriasis 13 41 0.042
768
c ACT004 Acute Diarrhea 39 0.042
769
c CHR098 Chronic Pyelonephritis 38 0.042
770
GRM010 Germ Cells Tumors 34 0.042
771
RSP007 Respiratory Distress Syndrome, Infant 30 0.042
772
LTH043 Lithium Transport 18 0.042
773
BRT054 Brittle Bone Disorder 72 0.040
774
ART016 Aortic Aneurysm 69 0.040
775
P MYC084 Mycobacterium Tuberculosis 1 68 0.040
776
P BLD062 Bile Duct Cancer 67 0.040
777
MYL031 Myeloproliferative Neoplasm 66 0.040
778
c JVN010 Juvenile Rheumatoid Arthritis 64 0.040
779
CLR108 Colorectal Adenoma 64 0.040
780
PLM031 Poliomyelitis 64 0.040
781
P SPN046 Spinal Muscular Atrophy 62 0.040
782
OST003 Osteonecrosis 61 0.040
783
INS001 Insulinoma 60 0.040
784
P BRS044 Breast Adenocarcinoma 59 0.040
785
SPT004 Septic Arthritis 58 0.040
786
HMR039 Hemorrhage, Intracerebral 57 0.040
787
PNM008 Pneumothorax 56 0.040
788
P ADL017 Adult T-Cell Leukemia 56 0.040
789
RSC001 Rosacea 54 0.040
790
P PMP001 Pemphigus 54 0.040
791
P INS002 in Situ Carcinoma 53 0.040
792
OCL006 Ocular Hypertension 53 0.040
793
P HYP083 Hypopituitarism 53 0.040
794
P SHR001 Short Bowel Syndrome 53 0.040
795
c VRL010 Viral Hepatitis 52 0.040
796
P RCT021 Rectum Cancer 52 0.040
797
CLR109 Colorectal Adenocarcinoma 51 0.040
798
ESP002 Esophageal Varix 51 0.040
799
c INF145 Infantile Liver Failure Syndrome 1 50 0.040
800
MCR004 Macroglobulinemia 49 0.040
801
c BCT013 Bacterial Pneumonia 48 0.040
802
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.040
803
BNN003 Bone Inflammation Disease 48 0.040
804
ANR004 Anuria 46 0.040
805
ASP008 Aspiration Pneumonitis 45 0.040
806
PPL001 Papillary Adenoma 44 0.040
807
BNM001 Bone Marrow Cancer 43 0.040
808
HMP009 Haemophilus Influenzae 43 0.040
809
P DST107 Distal Renal Tubular Acidosis 42 0.040
810
SPR126 Superior Semicircular Canal Dehiscence 40 0.040
811
c HMG029 Hemoglobin Se Disease 39 0.040
812
OVR094 Ovarian Epithelial Cancer 38 0.040
813
PLY150 Polykaryocytosis Inducer 31 0.040
815
NND001 Nondystrophic Myotonia 20 0.040
816
c FML159 Familial Periodic Paralyses 16 0.040
817
P SRC025 Sarcoidosis 1 70 0.038
818
c FML021 Familial Hypercholesterolemia 66 0.038
819
c MCL013 Mucolipidosis Iv 66 0.038
820
PPL049 Papillon-Lefevre Syndrome 65 0.038
821
NRM005 Neuromuscular Disease 64 0.038
822
P END044 Endometriosis 63 0.038
823
c ALP101 Alpha-Thalassemia 62 0.038
824
HSH003 Hashimoto Thyroiditis 62 0.038
825
ORL011 Oral Cancer 60 0.038
826
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 59 0.038
827
c DNG003 Dengue Disease 59 0.038
828
P PGT001 Paget's Disease of Bone 58 0.038
829
c DWL002 Dowling-Degos Disease 1 58 0.038
830
MNR012 Meniere Disease 57 0.038
831
NRL004 Neuroleptic Malignant Syndrome 56 0.038
832
MTH009 Mouth Disease 56 0.038
833
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.038
834
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.038
835
CLL003 Cellulitis 54 0.038
836
P EPD016 Epidermolysis Bullosa 53 0.038
837
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.038
838
MCN017 Meconium Ileus 52 0.038
839
CCC002 Coccidiosis 51 0.038
840
P THR015 Thrombophilia 51 0.038
841
FSC004 Fasciitis 50 0.038
842
c HRD202 Hereditary Lymphedema I 50 0.038
843
PRT018 Portal Vein Thrombosis 50 0.038
844
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.038
845
CHL004 Cholelithiasis 49 0.038
846
VTM033 Vitamin K Deficiency Bleeding 48 0.038
847
RYN005 Raynaud Phenomenon 47 0.038
848
ATN004 Autonomic Neuropathy 45 0.038
849
APP009 Appendix Adenocarcinoma 44 0.038
850
ORL015 Oral Squamous Cell Carcinoma 43 0.038
851
TRP009 Triple X Syndrome 42 0.038
852
DRG024 Drug Allergy 42 0.038
853
HYP264 Hypertonia 38 0.038
854
SCN067 Scn1a Seizure Disorders 19 0.038
855
ADR007 Adrenoleukodystrophy 75 0.037
856
c HPT073 Hepatitis C Virus 72 0.037
857
EWN003 Ewing Sarcoma 69 0.037
858
FCT007 Factor Vii Deficiency 67 0.037
859
FLL027 Fallopian Tube Carcinoma 67 0.037
860
P HYD006 Hydrocephalus 66 0.037
861
c ART101 Aortic Valve Disease 2 65 0.037
862
BRC012 Brucellosis 64 0.037
863
CYS013 Cystinuria 63 0.037
864
ANR007 Anorexia Nervosa 63 0.037
865
P ALP009 Alopecia Areata 60 0.037
866
CHC001 Chickenpox 60 0.037
867
P PTN014 Patent Ductus Arteriosus 1 60 0.037
868
ERY003 Erythema Multiforme 58 0.037
869
CHL028 Childhood Type Dermatomyositis 58 0.037
870
APP015 Apparent Mineralocorticoid Excess 58 0.037
871
LYM027 Lymphopenia 58 0.037
872
APH001 Aphthous Stomatitis 57 0.037
873
P MYS005 Myositis 56 0.037
874
CMR002 Coumarin Resistance 56 0.037
875
SCP002 Scapuloperoneal Spinal Muscular Atrophy 56 0.037
876
PRT038 Protein-Energy Malnutrition 54 0.037
877
BRD004 Borderline Personality Disorder 53 0.037
878
c CNT035 Central Nervous System Disease 52 0.037
879
THR004 Thrombocytosis 51 0.037
881
BRX001 Bruxism 50 0.037
882
CRN030 Coronary Stenosis 50 0.037
883
ATY042 Atypical Chronic Myeloid Leukemia 49 0.037
884
BCT004 Bacteriuria 49 0.037
885
RFR010 Refractory Anemia 48 0.037
886
SPL018 Splenomegaly 48 0.037
887
P HMN032 Human Herpesvirus 8 47 0.037
888
c PRM093 Premature Ovarian Failure 7 47 0.037
889
NWC001 Newcastle Disease 45 0.037
890
CRT015 Carotid Artery Occlusion 45 0.037
891
c DRM054 Dermatitis, Atopic, 2 44 0.037
892
c FML036 Familial Periodic Paralysis 44 0.037
893
DMP001 Dumping Syndrome 44 0.037
894
P MYG005 Myoglobinuria 44 0.037
895
DNT001 Dental Fluorosis 43 0.037
896
SNL007 Senile Cataract 42 0.037
897
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 40 0.037
898
ALD013 Aldosterone-Producing Adenoma 39 0.037
899
c OVR114 Ovarian Cancer 1 38 0.037
900
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.037
901
EXN003 Exencephaly 31 0.037
902
MNG007 Manganese Poisoning 29 0.037
903
OCC001 Occupational Dermatitis 29 0.037
904
CYT018 Cytochrome P450 2d6 Variant 27 0.037
905
P ATX030 Ataxia-Telangiectasia 82 0.035
906
P OCL013 Oculodentodigital Dysplasia 69 0.035
907
P INF038 Influenza 68 0.035
908
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.035
909
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.035
910
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.035
911
P ORT004 Orthostatic Intolerance 62 0.035
912
APP008 Appendicitis 61 0.035
913
P TXP001 Toxoplasmosis 60 0.035
914
P BNG030 Benign Ependymoma 60 0.035
915
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.035
916
ETN001 Eating Disorder 60 0.035
917
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.035
918
IDP011 Idiopathic Interstitial Pneumonia 59 0.035
919
P MTR012 Mitral Valve Disease 58 0.035
920
P BNC003 Bone Cancer 58 0.035
921
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.035
922
c CHR417 Chronic Graft Versus Host Disease 57 0.035
923
ARG007 Argininemia 57 0.035
924
APH002 Aphasia 57 0.035
925
PHR003 Pharyngitis 57 0.035
926
PLS011 Plasmacytoma 56 0.035
927
c ESS001 Essential Tremor 56 0.035
928
CHR100 Chronic Ulcer of Skin 55 0.035
929
P STR020 Strabismus 55 0.035
930
P SLM003 Salmonellosis 55 0.035
931
CLL010 Cellular Ependymoma 54 0.035
932
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.035
933
LYM022 Lymphangioma 54 0.035
934
P FML023 Familial Hemiplegic Migraine 53 0.035
935
BRN038 Bronchial Disease 53 0.035
936
HMC014 Homocysteinemia 53 0.035
937
IRD001 Iridocyclitis 53 0.035
938
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.035
939
P BRN035 Brain Stem Glioma 52 0.035
940
CND002 Conduct Disorder 51 0.035
941
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 51 0.035
942
GNT002 Giant Cell Glioblastoma 50 0.035
943
c SVR005 Severe Pre-Eclampsia 50 0.035
944
P MTR003 Mitral Valve Stenosis 50 0.035
945
STT002 Status Asthmaticus 50 0.035
946
HRT011 Heart Septal Defect 50 0.035
947
P END046 Endometritis 49 0.035
948
c NRC009 Narcolepsy 1 49 0.035
949
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.035
950
P THY054 Thyrotoxic Periodic Paralysis 46 0.035
951
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.035
952
PRP017 Periapical Periodontitis 46 0.035
953
P HMR005 Hemorrhoid 46 0.035
954
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.035
955
NSP002 Nasopharyngitis 43 0.035
956
LWC001 Low Compliance Bladder 43 0.035
957
MST004 Mast Cell Neoplasm 42 0.035
958
c MLG079 Malignant Pleural Mesothelioma 42 0.035
959
MCH006 Mechanical Strabismus 42 0.035
960
P HYP263 Hypersomnia 41 0.035
961
c FML297 Familial Thyroid Dyshormonogenesis 41 0.035
962
ART008 Arteriosclerosis Obliterans 40 0.035
963
AMN002 Amino Acid Metabolic Disorder 39 0.035
964
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.035
965
EXT007 Extracutaneous Mastocytoma 38 0.035
966
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.035
967
GLM044 Glomerular Disease 37 0.035
968
c HYP606 Hypokalemic Periodic Paralysis, Type 2 37 0.035
969
PRR001 Periarthritis 32 0.035
970
OSM001 Osmotic Diarrhea 32 0.035
971
TMP019 Temporomandibular Joint Anomaly 28 0.035
972
P ATR081 Atrial Standstill 28 0.035
973
ENM001 Enamel Caries 28 0.035
974
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.035
975
NRM009 Normokalemic Periodic Paralysis 28 0.035
976
EXF003 Exfoliative Dermatitis 27 0.035
977
HML018 Homologous Wasting Disease 22 0.035
978
AMN012 Aminoacidopathies 21 0.035
979
P INB001 Inborn Amino Acid Metabolism Disorder 10 0.035
980
P APL001 Aplastic Anemia 74 0.033
981
P FML011 Familial Adenomatous Polyposis 72 0.033
982
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.033
983
MYC006 Mycosis Fungoides 66 0.033
984
CHG001 Chagas Disease 66 0.033
985
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.033
986
P ERL057 Early Infantile Epileptic Encephalopathy 63 0.033
987
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.033
988
P PRM006 Primary Biliary Cirrhosis 62 0.033
989
WLD007 Waldenstroem's Macroglobulinemia 61 0.033
990
DCB001 Decubitus Ulcer 61 0.033
991
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 61 0.033
992
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.033
993
HYD002 Hydronephrosis 60 0.033
994
P HRD011 Hereditary Spherocytosis 60 0.033
995
c LNG047 Long Qt Syndrome 2 58 0.033
996
P GLL018 Gallbladder Cancer 57 0.033
997
P PLY018 Polycythemia 56 0.033
998
P FBR017 Fibrosarcoma 56 0.033
999
LST001 Listeriosis 56 0.033
1000
P MTC069 Mitochondrial Disorders 56 0.033
1001
HMG005 Hemoglobinopathy 56 0.033
1002
INT030 Intracranial Aneurysm 56 0.033
1003
P PTT006 Pituitary Adenoma 55 0.033
1004
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.033
1005
P CYS039 Cystic Kidney Disease 54 0.033
1006
BRN014 Bronchopneumonia 54 0.033
1007
PRC013 Pericarditis 54 0.033
1008
HMS001 Hemosiderosis 54 0.033
1009
P RNL017 Renal Oncocytoma 53 0.033
1010
P CNT005 Central Nervous System Lymphoma 53 0.033
1011
INF034 Infective Endocarditis 53 0.033
1012
MTN003 Motion Sickness 53 0.033
1013
c XNT010 Xanthinuria, Type I 53 0.033
1014
LMY002 Leiomyoma 52 0.033
1015
PLR008 Pleurisy 50 0.033
1016
RDC002 Radiculopathy 50 0.033
1017
PYD002 Pyoderma 50 0.033
1018
c CHR418 Chronic Leukemia 49 0.033
1019
VRC001 Varicocele 49 0.033
1020
PRP007 Priapism 47 0.033
1021
PRC003 Proctitis 47 0.033
1022
LYM012 Lymphoplasmacytic Lymphoma 47 0.033
1023
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.033
1024
RTN020 Retinal Vascular Disease 46 0.033
1025
CLN045 Colonic Benign Neoplasm 46 0.033
1026
MGC001 Megacolon 46 0.033
1027
P HYP733 Hypercalciuria, Absorptive, 2 45 0.033
1028
GLC022 Glucose/galactose Malabsorption 45 0.033
1029
MYF001 Myofibroma 45 0.033
1030
PTT037 Pituitary Tumors 44 0.033
1031
ANP009 Anaplastic Oligodendroglioma 43 0.033
1032
DVR002 Diverticulitis 43 0.033
1033
P MLT008 Multinodular Goiter 42 0.033
1034
DBT002 Diabetic Autonomic Neuropathy 41 0.033
1035
DFF003 Diffuse Scleroderma 41 0.033
1036
PST053 Postherpetic Neuralgia 40 0.033
1037
HYP540 Hypertension, Diastolic 40 0.033
1038
ACT011 Acute Contagious Conjunctivitis 40 0.033
1039
C1N001 C1 Inhibitor Deficiency 39 0.033
1040
PHT008 Photosensitive Epilepsy 39 0.033
1041
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.033
1043
P VSC018 Visceral Steatosis 33 0.033
1044
P RNL115 Renal Tubular Acidosis, Proximal 31 0.033
1045
STT009 Sutton Disease 2 30 0.033
1046
CLC004 Calcific Tendinitis 30 0.033
1047
P CNT036 Central Nervous System Germ Cell Tumor 28 0.033
1048
PRQ002 Paraquat Poisoning 26 0.033
1049
ADG002 Audiogenic Seizures 25 0.033
1050
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.031
1051
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.031
1052
c EXD008 Exudative Vitreoretinopathy 1 71 0.031
1053
P ASP006 Aspergillosis 69 0.031
1054
ACR008 Acrocallosal Syndrome 69 0.031
1055
OBS002 Obsessive-Compulsive Disorder 68 0.031
1056
PNC129 Pancreatic Adenocarcinoma 68 0.031
1057
P CNG001 Congenital Myasthenic Syndrome 66 0.031
1058
c LNG044 Long Qt Syndrome 1 66 0.031
1059
CRN036 Craniopharyngioma 65 0.031
1060
CHY002 Chylomicron Retention Disease 65 0.031
1061
c WLM013 Wilms Tumor 1 65 0.031
1062
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.031
1063
P MCH002 Machado-Joseph Disease 62 0.031
1064
c WLM018 Wilms Tumor 5 61 0.031
1065
SZR001 Sezary's Disease 60 0.031
1066
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.031
1067
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.031
1068
SPP011 Suppression of Tumorigenicity 12 59 0.031
1069
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.031
1070
INC002 Inclusion Body Myositis 58 0.031
1071
PST028 Post-Traumatic Stress Disorder 58 0.031
1072
PMP006 Pemphigus Vulgaris, Familial 57 0.031
1073
CHK001 Chikungunya 57 0.031
1074
CHR177 Chromophobe Renal Cell Carcinoma 57 0.031
1075
LMY014 Leiomyoma, Uterine 56 0.031
1076
ACS001 Acoustic Neuroma 56 0.031
1077
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.031
1078
BRN012 Bronchiolitis Obliterans 55 0.031
1079
PLV003 Pelvic Inflammatory Disease 55 0.031
1080
P MLN007 Male Infertility 55 0.031
1081
JVN009 Juvenile Pilocytic Astrocytoma 55 0.031
1082
ESN005