Search results for Potassium

2140 hits were found for Potassium

# Family MCID Name MIFTS Score
1
MYT030 Myotonia, Potassium-Aggravated 45 6.463
2
HYP005 Hypokalemia 55 5.923
3
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 4.364
4
OVR093 Overhydrated Hereditary Stomatocytosis 43 3.877
5
GTL001 Gitelman Syndrome 65 3.434
6
HYP052 Hyperkalemic Periodic Paralysis 61 2.086
7
P BRT004 Bartter Disease 52 2.048
8
KND001 Kindler Syndrome 64 2.010
9
SDM004 Sodium-Potassium-Atpase Activity of Red Cell 7 1.959
10
PTS020 Potassium Dichromate Allergic Contact Dermatitis 3 1.959
11
c NRL029 Neurological Muscular Channelopathy Due to a Genetic Potassium Channel Defect 3 1.951
12
c NRL037 Neurological Channelopathy of the Central Nervous System Due to a Genetic Potassium Channel Defect 2 1.951
13
NRM009 Normokalemic Periodic Paralysis 28 1.943
14
ALP077 Alpha-Methylacetoacetic Aciduria 55 1.933
15
c PRG143 Progressive Myoclonus Epilepsy 7 16 1.933
16
c EPL134 Epilepsy, Progressive Myoclonic 7 27 1.920
17
c HYP595 Hypertension, Essential 84 0.305
18
P KDN018 Kidney Disease 72 0.246
19
P LNG028 Long Qt Syndrome 66 0.232
20
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.208
21
P CRD119 Cardiac Arrest 67 0.206
22
HRW001 Hair Whorl 36 0.201
23
c ACT075 Acute Myocardial Infarction 57 0.198
24
CNG034 Congestive Heart Failure 69 0.197
25
ALL026 Allergic Hypersensitivity Disease 62 0.190
26
PRT037 Pertussis 65 0.184
27
c CHR684 Chronic Kidney Disease 70 0.181
28
HLX001 Helix Syndrome 47 0.174
29
MTB004 Metabolic Acidosis 50 0.173
30
P HRT032 Heart Disease 75 0.168
31
ANX004 Anoxia 40 0.167
32
ISC004 Ischemia 58 0.160
33
P PRD021 Periodic Paralysis 45 0.159
34
HYP266 Hypoxia 57 0.158
35
P ENC004 Encephalitis 61 0.157
36
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.157
37
NPH009 Nephrolithiasis 55 0.153
38
P MYC007 Myocardial Infarction 70 0.150
39
P DRR001 Diarrhea 55 0.147
40
HYP056 Hypoglycemia 66 0.146
41
P NRB001 Neuroblastoma 72 0.145
42
CRD223 Cardiac Arrhythmia 60 0.144
43
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.144
44
48X005 48,xyyy 39 0.144
45
CRD132 Cardiac Conduction Defect 58 0.143
46
P SZR006 Seizure Disorder 56 0.140
47
END086 End Stage Renal Disease 51 0.140
48
VSL002 Visual Epilepsy 59 0.139
49
LMB024 Limbic Encephalitis 41 0.138
50
P HYP076 Hyperthyroidism 55 0.133
51
LVR012 Liver Cirrhosis 62 0.127
52
c MGR028 Migraine with or Without Aura 1 67 0.126
53
P GLM045 Glioma 63 0.123
54
P ATR011 Atrial Fibrillation 66 0.122
55
GLL048 Glial Tumor 45 0.122
56
HYP066 Hyperglycemia 61 0.121
57
c GRV008 Graves Disease 1 56 0.121
58
P EPL164 Epilepsy 71 0.119
59
P HYP086 Hypothyroidism 69 0.118
60
P ENC018 Encephalopathy 61 0.118
61
P EPS003 Episodic Ataxia 59 0.117
62
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.110
63
HYP060 Hyperinsulinism 54 0.110
64
P LVR013 Liver Disease 68 0.109
65
ATM095 Autoimmune Disease 62 0.109
66
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.109
67
OCL069 Ocular Motor Apraxia 51 0.109
68
ANG054 Angina Pectoris 66 0.108
69
P CYS018 Cystitis 59 0.108
70
P DBT009 Diabetes Mellitus 64 0.107
71
PRS021 Prostatic Adenoma 51 0.105
72
PRS045 Prostatic Hypertrophy 53 0.104
73
PRS129 Prostatic Hyperplasia, Benign 49 0.104
74
c BRN108 Branchiootic Syndrome 1 62 0.103
75
LPP008 Lipoprotein Quantitative Trait Locus 62 0.103
76
ADN018 Adenoma 59 0.103
77
P INT143 Interstitial Cystitis 61 0.102
78
c ACT071 Acute Kidney Failure 60 0.101
79
P VSC007 Vascular Disease 63 0.100
80
DRM006 Dermatitis 61 0.100
81
c FML191 Familial Long Qt Syndrome 53 0.100
82
CRB004 Cerebral Artery Occlusion 45 0.100
83
DWN001 Down Syndrome 70 0.098
84
GTR002 Goiter 53 0.098
85
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.097
86
P RNL007 Renal Tubular Acidosis 51 0.097
87
URM002 Uremia 49 0.097
88
P GST053 Gastric Cancer 83 0.096
89
P PLM037 Pulmonary Hypertension 67 0.096
90
BNR002 Bone Resorption Disease 48 0.096
91
STR067 Stroke, Ischemic 81 0.095
92
P TMP001 Temporal Lobe Epilepsy 50 0.095
93
URL001 Urolithiasis 45 0.095
94
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.093
95
P DNT007 Dentin Sensitivity 36 0.093
96
CYS001 Cystic Fibrosis 81 0.091
97
P TRN020 Turner Syndrome 67 0.091
98
TXC005 Toxic Shock Syndrome 62 0.089
99
P CRD246 Cardiovascular System Disease 57 0.089
100
ATR057 Atrioventricular Block 55 0.089
101
HYP014 Hyperuricemia 52 0.089
102
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.088
103
ADL002 Adult Syndrome 70 0.088
104
TTN003 Tetanus 65 0.088
105
PPT005 Peptic Ulcer Disease 59 0.088
106
P PYL005 Pyelonephritis 56 0.088
107
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.087
108
CHL014 Cholera 59 0.085
109
c LNG047 Long Qt Syndrome 2 58 0.085
110
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.085
111
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.085
112
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.085
113
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.085
114
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.085
115
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.085
116
SPR010 Sporotrichosis 46 0.085
117
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.085
118
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.085
119
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.085
120
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.085
121
P OST002 Osteoporosis 74 0.084
122
P MYP004 Myopathy 70 0.084
123
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.084
124
P ADN016 Adenocarcinoma 64 0.084
125
P CRN300 Coronary Heart Disease 1 63 0.084
126
SPN186 Spinal Cord Injury 60 0.084
127
CNS004 Constipation 58 0.084
128
P GRV001 Graves' Disease 55 0.084
129
P THY054 Thyrotoxic Periodic Paralysis 46 0.084
130
c PRC016 Pre-Eclampsia 63 0.082
131
c PNS012 Paine Syndrome 61 0.082
132
STT001 Status Epilepticus 60 0.082
133
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.082
134
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.082
135
c EPS042 Episodic Ataxia, Type 1 60 0.081
136
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.081
137
BRN004 Brain Edema 56 0.081
138
P TRM003 Tremor 54 0.081
139
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.081
140
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.081
141
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.081
142
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.079
143
P MSC005 Muscular Dystrophy 66 0.079
144
c ACT068 Acute Cystitis 63 0.079
145
LWC001 Low Compliance Bladder 43 0.079
146
c SZR022 Seizures, Benign Familial Neonatal, 1 42 0.079
147
MYT011 Myotonia 34 0.079
148
CYN003 Cyanide Poisoning 24 0.079
149
c FML001 Familial Atrial Fibrillation 65 0.078
150
PRT036 Peritonitis 64 0.078
151
P NRP001 Neuropathy 56 0.078
152
P PHC003 Pheochromocytoma 71 0.076
153
ATH013 Atherosclerosis Susceptibility 65 0.076
154
CLT003 Colitis 62 0.076
155
MLL001 Molluscum Contagiosum 50 0.076
156
ADR040 Adrenal Gland Pheochromocytoma 46 0.076
157
P CHR345 Chronic Pain 44 0.076
158
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.075
159
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.075
160
P MYS003 Myasthenia Gravis 68 0.075
161
CRB039 Cerebrovascular Disease 67 0.075
162
HLC007 Helicobacter Pylori Infection 59 0.075
163
P GLM007 Glomerulonephritis 57 0.075
164
GLC003 Glucose Intolerance 54 0.075
165
P DST107 Distal Renal Tubular Acidosis 42 0.075
166
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.075
167
P CLR023 Colorectal Cancer 99 0.073
168
ULC004 Ulcerative Colitis 73 0.073
169
ALC007 Alcohol Dependence 66 0.073
170
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.073
171
P DBT005 Diabetes Insipidus 55 0.073
172
c FML036 Familial Periodic Paralysis 44 0.073
173
P BRS047 Breast Cancer 97 0.071
174
P ALZ034 Alzheimer Disease 88 0.071
175
PLM010 Pulmonary Edema 54 0.071
176
NPH003 Nephrocalcinosis 51 0.071
177
ILS001 Ileus 51 0.071
178
PLP001 Pulpitis 49 0.071
179
BRN071 Brain Injury 49 0.071
180
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.071
181
P RSP003 Respiratory Failure 74 0.070
182
c HYP836 Hypercholesterolemia, Familial, 1 73 0.070
183
ANX010 Anxiety 73 0.070
184
c RHB024 Rhabdomyosarcoma 2 67 0.070
185
P PRD008 Periodontitis 64 0.070
186
P NPH012 Nephrotic Syndrome 60 0.070
187
CNT047 Contact Dermatitis 58 0.070
188
TRM010 Traumatic Brain Injury 51 0.070
189
P PSD003 Pseudohypoaldosteronism 44 0.070
190
P HYP120 Hypoaldosteronism 36 0.070
191
GLB015 Glioblastoma Multiforme 75 0.068
192
OTT002 Otitis Media 72 0.068
193
PLM001 Pulmonary Tuberculosis 69 0.068
194
NTR005 Nutritional Deficiency Disease 62 0.068
195
P CTR002 Cataract 60 0.068
196
INS001 Insulinoma 60 0.068
197
P HDC001 Headache 57 0.068
198
DNT012 Dental Caries 53 0.068
199
ART140 Arteries, Anomalies of 52 0.068
200
P RNL015 Renal Hypertension 47 0.068
201
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.066
202
P MLT020 Multiple Sclerosis 72 0.066
203
P BRG001 Brugada Syndrome 71 0.066
204
P PNM007 Pneumonia 68 0.066
205
RCK004 Rickets 68 0.066
206
P PSR002 Psoriasis 62 0.066
207
P ESP024 Esophagitis 62 0.066
208
PST011 Pustulosis of Palm and Sole 52 0.066
209
HYP017 Hypophosphatemia 50 0.066
210
ATX019 Ataxia with Vitamin E Deficiency 42 0.066
211
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.066
212
ALL014 Allergic Encephalomyelitis 38 0.066
213
c ATM075 Autoimmune Encephalitis 38 0.066
214
c FML159 Familial Periodic Paralyses 16 0.066
215
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.064
216
HMN044 Human Immunodeficiency Virus Type 1 71 0.064
217
P LKM002 Leukemia 68 0.064
218
GST092 Gastroesophageal Reflux 67 0.064
219
DPR016 Depression 63 0.064
220
P BND020 Bone Disease 59 0.064
221
GLS018 Glass Syndrome 57 0.064
222
IRN002 Iron Metabolism Disease 57 0.064
223
P GST044 Gastritis 56 0.064
224
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.064
225
AMN003 Amnestic Disorder 54 0.064
226
P LTR001 Lateral Sclerosis 54 0.064
227
P DDN001 Duodenal Ulcer 52 0.064
228
P BNG026 Benign Neonatal Seizures 49 0.064
229
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.064
230
P AMY004 Amyloidosis 70 0.062
231
P RHN004 Rhinitis 57 0.062
232
P BPL003 Bipolar Disorder 56 0.062
233
IMP005 Impotence 52 0.062
234
PNG002 Pain Agnosia 51 0.062
235
c SHR030 Short Qt Syndrome 46 0.062
236
MYC005 Myocardial Stunning 46 0.062
237
P HMR005 Hemorrhoid 46 0.062
238
P MYC033 Myoclonus 46 0.062
239
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.062
240
c MJR024 Major Affective Disorder 9 41 0.062
241
c MJR022 Major Affective Disorder 8 38 0.062
242
P LKM071 Leukemia, Chronic Lymphocytic 79 0.060
243
AST005 Asthma 76 0.060
244
c ATR087 Atrial Standstill 1 75 0.060
245
GT001 Gout 64 0.060
246
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.060
247
P EXN002 Exanthem 57 0.060
248
SCH014 Schistosomiasis 57 0.060
249
INT007 Intermediate Coronary Syndrome 55 0.060
250
PPL022 Papilloma 54 0.060
251
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.060
252
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.060
253
c MCR120 Microvascular Complications of Diabetes 7 47 0.060
254
c DRR009 Diarrhea 6 46 0.060
255
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.060
256
CHL079 Children's Interstitial Lung Disease 26 0.060
257
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.058
258
P LYM118 Lymphoma 68 0.058
259
OST159 Osteogenic Sarcoma 66 0.058
260
P MNN013 Meningitis 66 0.058
261
P THY023 Thymoma 65 0.058
262
P PLY014 Polycystic Kidney Disease 62 0.058
263
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.058
264
GST023 Gastric Ulcer 53 0.058
265
c THY107 Thymoma, Familial 52 0.058
266
P LCT001 Lactic Acidosis 51 0.058
267
P ECL001 Eclampsia 50 0.058
268
P RNV001 Renovascular Hypertension 48 0.058
269
HYP025 Hyperphosphatemia 48 0.058
270
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 46 0.058
271
HDN002 Head Injury 46 0.058
272
SYN036 Syncope 45 0.058
273
PPL052 Papillomatosis, Confluent and Reticulated 33 0.058
274
P SCH015 Schizophrenia 74 0.056
275
DFC004 Deficiency Anemia 70 0.056
276
P FRG001 Fragile X Syndrome 70 0.056
277
NRM005 Neuromuscular Disease 64 0.056
278
P SNS001 Sensorineural Hearing Loss 60 0.056
279
PRM057 Paramyotonia Congenita of Von Eulenburg 58 0.056
280
P ALC033 Alcohol Use Disorder 58 0.056
281
BCT022 Bacterial Infectious Disease 56 0.056
282
AGN016 Aging 56 0.056
283
HRT012 Heart Valve Disease 53 0.056
284
c MCR113 Microvascular Complications of Diabetes 3 52 0.056
285
DMY004 Demyelinating Disease 52 0.056
286
DRM011 Dermatophytosis 52 0.056
287
47X002 47,xyy 49 0.056
288
P BNG032 Benign Mesothelioma 46 0.056
289
ANR004 Anuria 46 0.056
290
IDP073 Idiopathic Hypercalciuria 43 0.056
291
c MCR130 Microvascular Complications of Diabetes 6 41 0.056
292
c MCR133 Microvascular Complications of Diabetes 4 41 0.056
293
ALD013 Aldosterone-Producing Adenoma 39 0.056
295
P LNG032 Lung Cancer 98 0.054
296
P RHM011 Rheumatoid Arthritis 80 0.054
297
SCK003 Sickle Cell Anemia 74 0.054
298
P ATS364 Autism 70 0.054
299
BRN024 Bronchitis 68 0.054
300
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.054
301
P NTR004 Neutropenia 63 0.054
302
P HYP069 Hyperparathyroidism 63 0.054
303
ANR007 Anorexia Nervosa 63 0.054
304
P EPL140 Epilepsy, Idiopathic Generalized 62 0.054
305
P VSC011 Vasculitis 62 0.054
306
ACQ007 Acquired Immunodeficiency Syndrome 60 0.054
307
LNG099 Lung Disease 60 0.054
308
SQM006 Squamous Cell Carcinoma 60 0.054
309
GST045 Gastroenteritis 59 0.054
310
P PRP019 Peripheral Nervous System Disease 58 0.054
311
PRS047 Prostatitis 56 0.054
312
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 0.054
313
FCL014 Focal Epilepsy 54 0.054
314
c VRL010 Viral Hepatitis 52 0.054
315
P MSC003 Muscular Atrophy 52 0.054
316
THR004 Thrombocytosis 51 0.054
317
P SCK005 Sickle Cell Disease 50 0.054
318
LYM019 Lymphosarcoma 46 0.054
319
P HYP733 Hypercalciuria, Absorptive, 2 45 0.054
320
HPT004 Hepatic Coma 45 0.054
321
c PRM038 Primary Agammaglobulinemia 44 0.054
322
HMP009 Haemophilus Influenzae 43 0.054
323
c CHR098 Chronic Pyelonephritis 38 0.054
324
c INT059 Internal Hemorrhoid 34 0.054
326
CNN003 Conn's Syndrome 79 0.052
327
P PRK057 Parkinson Disease, Late-Onset 78 0.052
328
CRH001 Crohn's Disease 74 0.052
329
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.052
330
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.052
331
PLM031 Poliomyelitis 64 0.052
332
TRN015 Transient Cerebral Ischemia 63 0.052
333
HPT019 Hepatic Encephalopathy 60 0.052
334
THY029 Thyroid Carcinoma 59 0.052
335
P LDD007 Liddle Syndrome 1 59 0.052
336
P INT070 Intestinal Obstruction 58 0.052
337
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.052
338
TNS005 Tonsillitis 57 0.052
339
PHR003 Pharyngitis 57 0.052
340
P INF037 Inflammatory Bowel Disease 54 0.052
341
P AST007 Astrocytoma 51 0.052
342
SQM002 Squamous Cell Papilloma 46 0.052
343
SPS057 Spasticity 45 0.052
344
PTT037 Pituitary Tumors 44 0.052
345
MST020 Mast Cell Activation Syndrome 26 0.052
346
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.049
347
IMM167 Immune Deficiency Disease 78 0.049
348
OST012 Osteoarthritis 78 0.049
349
CRV035 Cervical Cancer 76 0.049
350
P GRF003 Graft-Versus-Host Disease 72 0.049
351
CRT072 Creutzfeldt-Jakob Disease 70 0.049
352
P SYS005 Systemic Scleroderma 68 0.049
353
P MCR115 Microvascular Complications of Diabetes 5 66 0.049
354
c DBT099 Diabetes Mellitus, Type I 65 0.049
355
P MVM001 Movement Disease 63 0.049
356
ERL001 Early Myoclonic Encephalopathy 62 0.049
357
LPD008 Lipid Metabolism Disorder 62 0.049
358
c SVR001 Severe Acute Respiratory Syndrome 62 0.049
359
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.049
360
FTT001 Fatty Liver Disease 61 0.049
361
P BCL017 B-Cell Lymphoma 58 0.049
362
P URT039 Urticaria 58 0.049
363
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.049
364
GST050 Gastrointestinal System Disease 56 0.049
365
P ART021 Arteriosclerosis 54 0.049
366
DBT010 Diabetic Neuropathy 54 0.049
367
c XNT010 Xanthinuria, Type I 53 0.049
368
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 51 0.049
369
STM007 Stomatitis 50 0.049
370
ECT026 Ectopic Pregnancy 50 0.049
371
INT067 Interstitial Nephritis 48 0.049
372
CRN019 Coronary Artery Vasospasm 46 0.049
373
GNG003 Gingival Recession 44 0.049
374
c SYS001 Systemic Lupus Erythematosus 86 0.047
375
INS024 Insulin-Like Growth Factor I 79 0.047
376
P HNT016 Huntington Disease 72 0.047
377
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.047
378
c LNG044 Long Qt Syndrome 1 66 0.047
379
P DYS154 Dystonia 65 0.047
380
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.047
381
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.047
382
MDD011 Mood Disorder 62 0.047
383
CHL068 Cholestasis 61 0.047
384
c ACT027 Acute Pancreatitis 60 0.047
385
P MYC008 Myocarditis 59 0.047
386
P SYP003 Syphilis 58 0.047
387
P END033 Endocarditis 57 0.047
388
ALL010 Allergic Contact Dermatitis 56 0.047
389
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.047
390
PRT038 Protein-Energy Malnutrition 54 0.047
391
PRP016 Paraplegia 52 0.047
392
DYS015 Dysentery 52 0.047
393
TLN003 Telangiectasis 52 0.047
394
P MGR003 Migraine with Aura 52 0.047
395
ENT011 Enterocolitis 51 0.047
396
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.047
397
NTR046 Neutrophil Migration 50 0.047
398
QDR001 Quadriplegia 48 0.047
399
TBR011 Tuberculous Meningitis 48 0.047
400
RNL077 Renal Fibrosis 47 0.047
401
CRD137 Cardiogenic Shock 47 0.047
402
SBC016 Subacute Delirium 44 0.047
403
CRB090 Cerebral Hypoxia 44 0.047
404
P HYP265 Hypotonia 43 0.047
405
CYT002 Cytokine Deficiency 42 0.047
406
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.047
407
HYP540 Hypertension, Diastolic 40 0.047
408
P FML187 Familial Hypertension 37 0.047
409
P PRD017 Periodic Paralyses 25 0.047
410
P HPT023 Hepatocellular Carcinoma 100 0.044
411
P PRS040 Prostate Cancer 97 0.044
412
c LKM061 Leukemia, Acute Myeloid 84 0.044
413
PRP027 Peripheral Vascular Disease 71 0.044
414
P SLP006 Sleep Apnea 69 0.044
415
LYM133 Lymphoma, Hodgkin, Classic 69 0.044
416
P MYC084 Mycobacterium Tuberculosis 1 68 0.044
417
P INF038 Influenza 68 0.044
418
c ATS007 Autism Spectrum Disorder 67 0.044
419
MSC007 Muscle Hypertrophy 64 0.044
420
OST017 Osteomyelitis 64 0.044
421
SKN016 Skin Disease 63 0.044
422
P END044 Endometriosis 63 0.044
423
P HMN010 Hemangioma 61 0.044
424
DPH001 Diphtheria 60 0.044
425
c HYP731 Hyperaldosteronism, Familial, Type I 60 0.044
426
c ACT073 Acute Leukemia 58 0.044
427
MNT002 Mental Depression 58 0.044
428
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.044
429
CMM005 Common Cold 57 0.044
430
ALL006 Allergic Asthma 56 0.044
431
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.044
432
P RNL017 Renal Oncocytoma 53 0.044
433
INF034 Infective Endocarditis 53 0.044
434
THY030 Thyroid Gland Disease 52 0.044
435
PTH003 Pathologic Nystagmus 52 0.044
436
c PYR010 Peyronie's Disease 50 0.044
437
P OVR082 Overgrowth Syndrome 50 0.044
438
PYD002 Pyoderma 50 0.044
439
P NNT009 Neonatal Diabetes Mellitus 50 0.044
440
c BNG006 Benign Familial Neonatal Epilepsy 50 0.044
441
P MYT002 Myotonic Dystrophy 49 0.044
442
CLS016 Clostridium Difficile Colitis 48 0.044
443
PYL006 Pyloric Stenosis 48 0.044
444
c BRT050 Bartter Syndrome, Type 2, Antenatal 46 0.044
445
c DBT103 Diabetes Mellitus, Permanent Neonatal 4 46 0.044
446
c MLG068 Malignant Glioma 46 0.044
447
KWS001 Kwashiorkor 44 0.044
448
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.044
450
LPT014 Leptin Deficiency or Dysfunction 74 0.041
451
P ART022 Arthritis 69 0.041
452
CRB037 Cerebral Palsy 69 0.041
453
P OCL013 Oculodentodigital Dysplasia 69 0.041
454
CNN005 Connective Tissue Disease 68 0.041
455
P MLG056 Malignant Hyperthermia 67 0.041
456
WLF001 Wolff-Parkinson-White Syndrome 66 0.041
457
P DMN002 Dementia 66 0.041
458
P CNJ013 Conjunctivitis 65 0.041
459
P MTR014 Motor Neuron Disease 65 0.041
460
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.041
461
P HML002 Hemolytic Anemia 63 0.041
462
P HYP750 Hypertriglyceridemia, Familial 62 0.041
463
P MYL006 Myeloid Leukemia 60 0.041
464
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.041
465
P SLP005 Sleep Disorder 59 0.041
466
P DBT100 Diabetes Mellitus, Permanent Neonatal 1 59 0.041
467
MNR012 Meniere Disease 57 0.041
468
CMR002 Coumarin Resistance 56 0.041
469
P MYT023 Myotonia Congenita 56 0.041
470
P SCK002 Sick Sinus Syndrome 55 0.041
471
P PMP001 Pemphigus 54 0.041
472
NNL006 Non-Alcoholic Steatohepatitis 54 0.041
473
P RTN016 Retinal Degeneration 53 0.041
474
MRG003 Marginal Zone B-Cell Lymphoma 52 0.041
475
P RCT021 Rectum Cancer 52 0.041
476
PPT001 Peptic Esophagitis 52 0.041
477
KRT009 Keratosis 51 0.041
478
PNN001 Panniculitis 51 0.041
479
TRY001 Trypanosomiasis 50 0.041
480
DYS073 Dysphagia 50 0.041
481
c SPN311 Spinocerebellar Ataxia 13 50 0.041
482
c BRT042 Bartter Syndrome, Type 3 46 0.041
483
ACT003 Acute Kidney Tubular Necrosis 45 0.041
484
49X006 49, Xxxxy Syndrome 41 0.041
485
P DYS021 Dysautonomia 39 0.041
486
VLK001 Volkmann Contracture 25 0.041
487
OBN001 Ouabain Resistance 18 0.041
488
P OVR042 Ovarian Cancer 88 0.038
489
MYL069 Myeloma, Multiple 85 0.038
490
P BLD134 Bladder Cancer 79 0.038
491
BRN028 Brain Cancer 74 0.038
492
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.038
493
MNT001 Mantle Cell Lymphoma 69 0.038
494
P HPT021 Hepatitis 67 0.038
495
P HYP098 Hypereosinophilic Syndrome 67 0.038
496
P NSP012 Nasopharyngeal Carcinoma 66 0.038
497
CHG001 Chagas Disease 66 0.038
498
P PLM036 Pulmonary Fibrosis 65 0.038
499
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.038
500
SRC014 Sarcoma 65 0.038
501
IRR002 Irritable Bowel Syndrome 65 0.038
502
c FNC043 Fanconi Anemia, Complementation Group E 62 0.038
503
P PNC044 Pancreatitis 61 0.038
504
GST033 Gestational Diabetes 61 0.038
505
SDD001 Sudden Infant Death Syndrome 61 0.038
506
P LPS004 Lupus Erythematosus 61 0.038
507
VRC005 Varicose Veins 60 0.038
508
ETN001 Eating Disorder 60 0.038
509
P BNC003 Bone Cancer 58 0.038
510
c DWL002 Dowling-Degos Disease 1 58 0.038
511
P ESP035 Esophagitis, Eosinophilic, 1 57 0.038
512
P ANG015 Angioedema 57 0.038
513
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.038
514
URN010 Urinary Tract Obstruction 55 0.038
515
AMN001 Amenorrhea 54 0.038
516
SNS003 Sensory Peripheral Neuropathy 54 0.038
517
FNG017 Fungal Infectious Disease 53 0.038
518
SPN035 Spindle Cell Sarcoma 53 0.038
519
P THY032 Thyroiditis 52 0.038
520
CRN030 Coronary Stenosis 50 0.038
521
c SVR005 Severe Pre-Eclampsia 50 0.038
522
ENT004 Enthesopathy 49 0.038
523
WTH001 Withdrawal Disorder 48 0.038
524
ASP007 Aspiration Pneumonia 48 0.038
525
c MLG069 Malignant Hypertension 47 0.038
526
RTN023 Retinitis 46 0.038
527
ATN005 Autonomic Dysfunction 46 0.038
528
RTN020 Retinal Vascular Disease 46 0.038
529
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 46 0.038
530
BRN032 Brain Glioma 45 0.038
531
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.038
532
c BRT052 Bartter Syndrome, Type 1, Antenatal 43 0.038
533
TRP009 Triple X Syndrome 42 0.038
534
NRR001 Neuroretinitis 42 0.038
535
MDL009 Medullary Sponge Kidney 40 0.038
536
PRM020 Premenstrual Tension 40 0.038
537
c PSD092 Pseudohypoaldosteronism, Type Iie 39 0.038
538
c HYP438 Hyperaldosteronism, Familial, Type Iii 35 0.038
539
c THY084 Thyrotoxic Periodic Paralysis 1 35 0.038
541
MTH071 Methane Production 26 0.038
542
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.038
543
URT049 Urate Oxidase, Pseudogene 25 0.038
544
ADG002 Audiogenic Seizures 25 0.038
545
PRN068 Paraneoplastic Limbic Encephalitis 21 0.038
546
CNV009 Convulsions Benign Familial Neonatal Dominant Form 17 0.038
547
KCN019 Kcnk9 Imprinting Syndrome 13 0.038
548
P PNC035 Pancreatic Cancer 84 0.035
549
c DLT002 Dilated Cardiomyopathy 79 0.035
550
P RTN008 Retinitis Pigmentosa 79 0.035
551
P LNG064 Lung Cancer Susceptibility 3 78 0.035
552
P MDL005 Medulloblastoma 77 0.035
553
MSC157 Muscular Dystrophy, Duchenne Type 72 0.035
554
c LKM063 Leukemia, Chronic Myeloid 72 0.035
555
WLS001 Wilson Disease 71 0.035
556
P SRC025 Sarcoidosis 1 70 0.035
557
GST040 Gastric Adenocarcinoma 70 0.035
558
P MLN008 Melanoma 69 0.035
559
P LPR021 Leprosy 3 69 0.035
560
BRK010 Burkitt Lymphoma 67 0.035
561
P FLL037 Follicular Lymphoma 67 0.035
562
ALL003 Allergic Rhinitis 67 0.035
563
PSY004 Psychotic Disorder 67 0.035
564
c MCR129 Microvascular Complications of Diabetes 1 66 0.035
565
KRT019 Keratitis, Hereditary 65 0.035
566
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.035
567
c ART101 Aortic Valve Disease 2 65 0.035
568
P ADL010 Adult Respiratory Distress Syndrome 65 0.035
569
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.035
570
c EPS035 Episodic Ataxia, Type 2 63 0.035
571
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.035
572
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.035
573
c HPT001 Hepatitis C 62 0.035
574
c HPT003 Hepatitis a 62 0.035
575
APP008 Appendicitis 61 0.035
576
ACN002 Acanthosis Nigricans 60 0.035
577
HYD002 Hydronephrosis 60 0.035
578
PLM033 Pulmonary Embolism 59 0.035
579
GNG013 Gingivitis 59 0.035
580
BRN002 Bronchiolitis 59 0.035
581
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.035
582
P ANP001 Anaplastic Large Cell Lymphoma 58 0.035
583
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.035
584
BNG009 Benign Epilepsy with Centrotemporal Spikes 58 0.035
585
P CND004 Candidiasis 58 0.035
586
P INF032 Infertility 57 0.035
587
CHL067 Cholecystitis 57 0.035
588
c VSC019 Vesicoureteral Reflux 1 57 0.035
589
THR024 Thrombosis 57 0.035
590
CHR177 Chromophobe Renal Cell Carcinoma 57 0.035
591
VSC002 Vascular Dementia 57 0.035
592
c INT072 Intestinal Pseudo-Obstruction 56 0.035
593
MCR141 Mucormycosis 56 0.035
594
P HYP024 Hypoparathyroidism 56 0.035
595
P MYP006 Myopia 55 0.035
596
LYM040 Lymphoblastic Lymphoma 54 0.035
597
c LNG048 Long Qt Syndrome 3 53 0.035
598
INT075 Intracranial Hypertension 53 0.035
599
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.035
600
MCN017 Meconium Ileus 52 0.035
601
SPL004 Splenic Marginal Zone Lymphoma 51 0.035
602
HYP781 Hypoascorbemia 51 0.035
603
INT071 Intestinal Perforation 51 0.035
604
c ALM001 Al Amyloidosis 50 0.035
605
ALL009 Allergic Conjunctivitis 50 0.035
606
c CNG027 Congenital Hemolytic Anemia 50 0.035
607
VLV047 Volvulus of Midgut 49 0.035
608
c FLL041 Follicular Lymphoma 1 49 0.035
609
VCC001 Vaccinia 49 0.035
610
KRT002 Keratomalacia 47 0.035
611
PLS025 Plasmablastic Lymphoma 47 0.035
612
c PRM093 Premature Ovarian Failure 7 47 0.035
613
P MTH007 Methemoglobinemia 46 0.035
614
NWC001 Newcastle Disease 45 0.035
615
PRL008 Paralytic Ileus 45 0.035
616
c PCH010 Pachyonychia Congenita 3 44 0.035
617
CVD001 Covid-19 44 0.035
618
IDP033 Idiopathic Edema 44 0.035
619
DVR002 Diverticulitis 43 0.035
620
ORL015 Oral Squamous Cell Carcinoma 43 0.035
621
SNL007 Senile Cataract 42 0.035
622
c FML294 Familial Short Qt Syndrome 41 0.035
623
PRS063 Paresthesia 41 0.035
624
c MCR112 Microvascular Complications of Diabetes 2 41 0.035
625
ENT001 Enterocele 39 0.035
626
HRN029 Hearing Loss, Noise-Induced 37 0.035
627
CHR178 Chromosomal Triplication 35 0.035
628
HNS001 Hansen's Disease 34 0.035
629
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.035
630
P VSC018 Visceral Steatosis 33 0.035
631
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.035
632
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.035
633
CYT018 Cytochrome P450 2d6 Variant 27 0.035
634
c BRT024 Bartter Syndrome Type 4 20 0.035
635
CRM010 Cramp-Fasciculation Syndrome 16 0.035
636
ESP021 Esophageal Cancer 90 0.031
637
NRL016 Neural Tube Defects 82 0.031
638
c NRF023 Neurofibromatosis, Type Ii 80 0.031
639
GST019 Gastrointestinal Stromal Tumor 78 0.031
640
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.031
641
END057 Endometrial Cancer 74 0.031
642
c THR092 Thrombophilia Due to Thrombin Defect 73 0.031
643
c HPT073 Hepatitis C Virus 72 0.031
644
ACR007 Acromegaly 71 0.031
645
MYL009 Myelodysplastic Syndrome 70 0.031
646
P LKM062 Leukemia, Acute Lymphoblastic 69 0.031
647
P ESS003 Essential Thrombocythemia 68 0.031
648
P MJR001 Major Depressive Disorder 68 0.031
649
MYC006 Mycosis Fungoides 66 0.031
650
LPT001 Leptospirosis 66 0.031
651
P SKN015 Skin Carcinoma 66 0.031
652
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.031
653
P HYD006 Hydrocephalus 66 0.031
654
P DRM053 Dermatitis, Atopic 66 0.031
655
MYL031 Myeloproliferative Neoplasm 66 0.031
656
P NRV007 Nervous System Disease 66 0.031
657
c SML038 Small Cell Cancer of the Lung 65 0.031
658
KHL003 Kohlschutter-Tonz Syndrome 65 0.031
659
P MTR004 Maturity-Onset Diabetes of the Young 65 0.031
660
P HRP006 Herpes Simplex 65 0.031
661
APN008 Apnea, Obstructive Sleep 64 0.031
662
P ANR048 Aniridia 1 63 0.031
663
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.031
664
TYP007 Typhoid Fever 63 0.031
665
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.031
666
P MCH002 Machado-Joseph Disease 62 0.031
667
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.031
668
P ART023 Arthropathy 62 0.031
669
P PRM006 Primary Biliary Cirrhosis 62 0.031
670
OST003 Osteonecrosis 61 0.031
671
WST001 West Syndrome 61 0.031
672
YLL002 Yellow Fever 61 0.031
673
VRL011 Viral Infectious Disease 61 0.031
674
RHM001 Rheumatic Fever 60 0.031
675
SPP011 Suppression of Tumorigenicity 12 59 0.031
676
PRT013 Portal Hypertension 59 0.031
677
c DNG003 Dengue Disease 59 0.031
678
CHL123 Chlamydia 59 0.031
679
P BRS044 Breast Adenocarcinoma 59 0.031
680
P GLL022 Guillain-Barre Syndrome 59 0.031
681
ANR040 Aneurysm 59 0.031
682
BLR008 Bilirubin Metabolic Disorder 57 0.031
683
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.031
684
c FML035 Familial Hyperlipidemia 55 0.031
685
ANG005 Anogenital Venereal Wart 55 0.031
686
ESN005 Eosinophilic Gastroenteritis 55 0.031
687
P DRM007 Dermatitis Herpetiformis 55 0.031
688
P SLM003 Salmonellosis 55 0.031
689
PRP030 Purpura 54 0.031
690
RSC001 Rosacea 54 0.031
691
PYD001 Pyoderma Gangrenosum 54 0.031
692
THR013 Thoracic Outlet Syndrome 54 0.031
693
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.031
694
P FML023 Familial Hemiplegic Migraine 53 0.031
695
OCL006 Ocular Hypertension 53 0.031
696
MST005 Mastitis 53 0.031
697
c PRD040 Periodontitis, Chronic 53 0.031
698
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.031
699
P ACT008 Actinic Keratosis 53 0.031
700
P RTN018 Retinal Disease 53 0.031
701
ACR041 Acromelic Frontonasal Dysostosis 52 0.031
702
ONC002 Onchocerciasis 52 0.031
703
PLS009 Plasma Cell Neoplasm 51 0.031
704
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.031
705
NRM004 Neuroma 51 0.031
706
c SCN007 Secondary Hyperparathyroidism 51 0.031
707
HPT014 Hepatorenal Syndrome 50 0.031
708
c INF145 Infantile Liver Failure Syndrome 1 50 0.031
709
PLC008 Placenta Disease 50 0.031
710
SNT005 Sinoatrial Node Disease 49 0.031
711
CHL004 Cholelithiasis 49 0.031
712
LRN003 Learning Disability 49 0.031
713
c BCT013 Bacterial Pneumonia 48 0.031
714
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.031
715
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.031
716
CHR031 Chromoblastomycosis 47 0.031
717
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.031
718
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.031
719
MNG006 Monogenic Diabetes 46 0.031
720
URT010 Ureteral Obstruction 45 0.031
721
CYN002 Cyanosis, Transient Neonatal 45 0.031
722
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.031
723
ATN004 Autonomic Neuropathy 45 0.031
724
PNC085 Penicillin Allergy 45 0.031
725
GRN017 Granulocytopenia 44 0.031
726
P BCT020 Bacteremia 2 44 0.031
727
GRN007 Granuloma Annulare 44 0.031
728
P MYG005 Myoglobinuria 44 0.031
729
BCK006 Back Pain 42 0.031
730
BRK002 Birk-Barel Syndrome 41 0.031
731
RDN001 Reading Disorder 40 0.031
732
FNG016 Fungal Keratitis 40 0.031
733
LKP003 Leukoplakia 39 0.031
734
WLL004 Wallerian Degeneration 39 0.031
735
HYP344 Hyperthyroidism, Familial Gestational 39 0.031
736
AMN006 Aminoaciduria 38 0.031
737
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.031
738
P ANT061 Antenatal Bartter Syndrome 37 0.031
739
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 37 0.031
740
SCR003 Secretory Diarrhea 37 0.031
741
P MXL015 Maxillary Sinusitis 36 0.031
742
c DRM040 Dermatitis Herpetiformis, Familial 35 0.031
743
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.031
744
c PRG106 Progressive Muscular Dystrophy 33 0.031
745
c THY083 Thyrotoxic Periodic Paralysis 2 31 0.031
746
PLY150 Polykaryocytosis Inducer 31 0.031
747
SLC024 Slc4a1-Associated Distal Renal Tubular Acidosis 19 0.031
748
P ATX030 Ataxia-Telangiectasia 82 0.027
749
P GLM040 Glioma Susceptibility 1 81 0.027
750
SVR004 Severe Combined Immunodeficiency 73 0.027
751
c SPN225 Spondyloarthropathy 1 73 0.027
752
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.027
753
MYL005 Myelofibrosis 70 0.027
754
P TTR001 Tetralogy of Fallot 70 0.027
755
P TBR001 Tuberous Sclerosis 70 0.027
756
PLY001 Polycythemia Vera 69 0.027
757
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.027
758
ART016 Aortic Aneurysm 69 0.027
759
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.027
760
P ANG001 Angelman Syndrome 69 0.027
761
PNC129 Pancreatic Adenocarcinoma 68 0.027
762
P THR014 Thrombocytopenia 67 0.027
763
GLL008 Gilles De La Tourette Syndrome 66 0.027
764
PPL049 Papillon-Lefevre Syndrome 65 0.027
765
P LPS002 Liposarcoma 65 0.027
766
BRR014 Barrett Esophagus 65 0.027
767
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.027
768
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.027
769
CLN015 Colon Adenocarcinoma 65 0.027
770
P CHR071 Charcot-Marie-Tooth Disease 65 0.027
771
P RHB003 Rhabdomyosarcoma 63 0.027
772
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.027
773
HMT002 Hematologic Cancer 62 0.027
774
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.027
775
c DYS056 Dystonia 12 62 0.027
776
P BCK002 Beckwith-Wiedemann Syndrome 62 0.027
777
MSL001 Measles 62 0.027
778
INT002 Intermittent Claudication 61 0.027
779
TMT001 Timothy Syndrome 61 0.027
780
CHR066 Chronic Fatigue Syndrome 61 0.027
781
WLD007 Waldenstroem's Macroglobulinemia 61 0.027
782
PNM010 Pneumothorax, Primary Spontaneous 60 0.027
783
SZR001 Sezary's Disease 60 0.027
784
TRG002 Trigeminal Neuralgia 60 0.027
785
INT066 Interstitial Lung Disease 60 0.027
786
ING001 Inguinal Hernia 60 0.027
787
P CHR285 Chronic Myelomonocytic Leukemia 60 0.027
788
IDP011 Idiopathic Interstitial Pneumonia 59 0.027
789
c HPT016 Hepatitis B 59 0.027
790
P BRN022 Bronchiectasis 59 0.027
791
CYS010 Cystinosis 59 0.027
792
c SPN301 Spinocerebellar Ataxia 2 58 0.027
793
PST028 Post-Traumatic Stress Disorder 58 0.027
794
FBR047 Fibromyalgia 58 0.027
795
CHR072 Chordoma 58 0.027
796
NWB001 Newborn Respiratory Distress Syndrome 58 0.027
797
P GLL020 Gallbladder Disease 57 0.027
798
P PLV020 Pelvic Organ Prolapse 57 0.027
799
BLM002 Bulimia Nervosa 57 0.027
800
BRN056 Bronchopulmonary Dysplasia 57 0.027
801
P PLY041 Polymyositis 57 0.027
802
c MST023 Mesothelioma, Malignant 57 0.027
803
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.027
804
PNM008 Pneumothorax 56 0.027
805
P PLY018 Polycythemia 56 0.027
806
P ADL017 Adult T-Cell Leukemia 56 0.027
807
LST001 Listeriosis 56 0.027
808
PLS011 Plasmacytoma 56 0.027
809
c ACT134 Acute Liver Failure 56 0.027
810
ADN027 Adenomyosis 56 0.027
811
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.027
812
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.027
813
P NRF002 Neurofibromatosis 56 0.027
814
P PNM006 Pneumoconiosis 56 0.027
815
P PLY019 Polyneuropathy 56 0.027
816
NRN004 Neuroendocrine Tumor 55 0.027
817
P MLN007 Male Infertility 55 0.027
818
c BCT007 Bacterial Meningitis 55 0.027
819
HMP005 Hemiplegia 55 0.027
820
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.027
821
CRT017 Cartilage Disease 54 0.027
822
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.027
823
PRC013 Pericarditis 54 0.027
824
CLL003 Cellulitis 54 0.027
825
P TCD001 Tic Disorder 53 0.027
826
P HMR003 Hemorrhagic Disease 53 0.027
827
NRT001 Neurotic Disorder 53 0.027
828
TXC002 Toxic Encephalopathy 53 0.027
829
ALC009 Alcoholic Liver Cirrhosis 53 0.027
830
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.027
831
NRT004 Neuritis 52 0.027
832
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.027
833
P HMP007 Hemophilia 51 0.027
834
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.027
835
THR016 Thrombophlebitis 51 0.027
836
ACH005 Achalasia 51 0.027
837
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.027
838
HYP081 Hypolipoproteinemia 51 0.027
839
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.027
840
P HYP077 Hypertrichosis 50 0.027
841
c PRM012 Primary Polycythemia 50 0.027
842
AZS001 Azoospermia 50 0.027
843
OPT003 Opiate Dependence 50 0.027
844
c DYS119 Dystonia 9 50 0.027
845
P OTS001 Otosclerosis 49 0.027
846
ATY042 Atypical Chronic Myeloid Leukemia 49 0.027
847
URT001 Urethritis 49 0.027
848
c THR090 Thrombocythemia 1 49 0.027
849
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.027
850
GYN001 Gynecomastia 49 0.027
851
CCN002 Cocaine Abuse 49 0.027
852
P OPN001 Open-Angle Glaucoma 49 0.027
853
MCR004 Macroglobulinemia 49 0.027
854
c BPL002 Bipolar I Disorder 49 0.027
855
ACT029 Acute Interstitial Pneumonia 49 0.027
856
P CMP008 Compartment Syndrome 49 0.027
857
BCT004 Bacteriuria 49 0.027
858
P CTN015 Cutaneous T Cell Lymphoma 49 0.027
859
P CNT056 Cantu Syndrome 48 0.027
860
c ACT150 Acute Adrenal Insufficiency 48 0.027
861
INT054 Intraocular Lymphoma 48 0.027
862
ATS010 Autosomal Recessive Disease 48 0.027
863
CHR563 Chronic Eosinophilic Leukemia 48 0.027
864
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.027
865
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.027
866
BLD044 Bladder Disease 48 0.027
867
P MRC003 Mercury Poisoning 48 0.027
868
ANT018 Anthracosis 48 0.027
869
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.027
870
THY128 Thyroid Tumor 47 0.027
871
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.027
872
P CRC039 Coarctation of Aorta 47 0.027
873
P OVR046 Ovarian Cyst 47 0.027
874
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.027
875
P VTR007 Vitreoretinopathy 46 0.027
876
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.027
877
TNP001 Tinea Pedis 46 0.027
878
PRP017 Periapical Periodontitis 46 0.027
879
CLN045 Colonic Benign Neoplasm 46 0.027
880
EXT010 Extramedullary Plasmacytoma 45 0.027
881
LYM051 Lymphomatoid Granulomatosis 45 0.027
882
CRT015 Carotid Artery Occlusion 45 0.027
883
CNT017 Central Nervous System Origin Vertigo 45 0.027
884
ASP008 Aspiration Pneumonitis 45 0.027
885
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.027
886
c HYP272 Hypercholesterolemia, Familial, 3 44 0.027
887
DMP001 Dumping Syndrome 44 0.027
888
MYX004 Myxedema 43 0.027
889
BNM001 Bone Marrow Cancer 43 0.027
890
P CND005 Cone Dystrophy 43 0.027
891
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.027
892
P MJR007 Major Affective Disorder 1 43 0.027
894
MRS001 Marasmus 42 0.027
895
CHR286 Chronic Neutrophilic Leukemia 42 0.027
896
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.027
897
c LNG053 Long Qt Syndrome 9 41 0.027
898
GST020 Gastric Antral Vascular Ectasia 41 0.027
899
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.027
900
RST023 Resting Heart Rate, Variation in 41 0.027
901
CRN322 Coronavirus Infectious Disease 40 0.027
902
VLL006 Villous Adenoma 40 0.027
903
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.027
904
ANG049 Angioedema Induced by Ace Inhibitors 40 0.027
905
P FML156 Familial Hyperaldosteronism 39 0.027
906
CRV045 Cervical Intraepithelial Neoplasia 39 0.027
907
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.027
908
SCR011 Scrapie 39 0.027
909
URT004 Urethral Syndrome 38 0.027
910
VLV042 Vulvar Vestibulitis Syndrome 38 0.027
911
TNC002 Tinea Capitis 38 0.027
912
P PST059 Pustular Psoriasis 37 0.027
913
ATM052 Autoimmune Disease 1 37 0.027
914
P CRB088 Cerebral Atrophy 37 0.027
915
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.027
916
TMP011 Temple-Baraitser Syndrome 36 0.027
917
DRM009 Dermatomycosis 36 0.027
918
ABD010 Abdominal Wall Defect 36 0.027
919
MYT003 Myotonic Disease 35 0.027
920
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.027
921
CRY019 Cryohydrocytosis 34 0.027
922
c LKM005 Leukemia, T-Cell, Chronic 34 0.027
923
PST010 Pasteurellosis 34 0.027
924
BNN005 Bunion 33 0.027
925
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.027
926
HND015 Hand Skill, Relative 33 0.027
927
CND006 Candida Glabrata 32 0.027
928
CNG064 Congenital Chloride Diarrhea 32 0.027
929
c PSD090 Pseudohypoaldosteronism, Type Iia 32 0.027
930
CLN006 Colonic Pseudo-Obstruction 32 0.027
931
c PSD093 Pseudohypoaldosteronism, Type Iid 31 0.027
932
P RNL115 Renal Tubular Acidosis, Proximal 31 0.027
933
INF021 Infant Gynecomastia 31 0.027
934
KPP002 Keppen-Lubinsky Syndrome 31 0.027
935
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 30 0.027
936
FNT004 Fainting 30 0.027
937
PST092 Posttransplant Acute Limbic Encephalitis 29 0.027
938
EPL230 Epilepsy with Myoclonic-Atonic Seizures 28 0.027
939
c LNG052 Long Qt Syndrome 8 27 0.027
940
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.027
941
c HRD219 Hereditary Distal Renal Tubular Acidosis 27 0.027
942
MYP026 Myopathy - Thyrotoxic 17 0.027
943
DGT004 Digitalis Poisoning 14 0.027
944
HRD103 Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum 13 0.027
945
NNP018 Non-Paraneoplastic Limbic Encephalitis 12 0.027
947
MLR004 Malaria 81 0.022
948
P RTT002 Rett Syndrome 80 0.022
949
MRF001 Marfan Syndrome 77 0.022
950
c TBR025 Tuberous Sclerosis 1 77 0.022
951
ADR007 Adrenoleukodystrophy 75 0.022
952
P APL001 Aplastic Anemia 74 0.022
953
P FML018 Familial Mediterranean Fever 73 0.022
954
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.022
955
EWN003 Ewing Sarcoma 69 0.022
956
c MYT021 Myotonic Dystrophy 1 69 0.022
957
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.022
958
SKN019 Skin Melanoma 68 0.022
959
P ALP004 Alport Syndrome 68 0.022
960
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.022
961
FCT007 Factor Vii Deficiency 67 0.022
962
c HMP029 Hemophilia a 67 0.022
963
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.022
964
LYS012 Lysosomal Acid Lipase Deficiency 65 0.022
965
ANG020 Angiosarcoma 64 0.022
966
CLR108 Colorectal Adenoma 64 0.022
967
BRC012 Brucellosis 64 0.022
968
ART002 Arts Syndrome 64 0.022
969
CYS013 Cystinuria 63 0.022
970
ACT119 Acute Promyelocytic Leukemia 63 0.022
971
HYP780 Hypoadrenocorticism, Familial 63 0.022
972
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.022
973
P TRC086 Trichohepatoenteric Syndrome 1 62 0.022
974
HYD038 Hydrops Fetalis, Nonimmune 62 0.022
975
P DRM010 Dermatomyositis 61 0.022
976
NRM001 Neuromyelitis Optica 61 0.022
977
P CHL002 Childhood Absence Epilepsy 61 0.022
978
c SCL052 Scleroderma, Familial Progressive 61 0.022
979
ALC006 Alcoholic Hepatitis 61 0.022
980
RTN017 Retinal Detachment 61 0.022
981
P KDN017 Kidney Cancer 60 0.022
982
HRP004 Herpes Zoster 60 0.022
983
WLL001 Williams-Beuren Syndrome 60 0.022
984
P VNT002 Ventricular Septal Defect 60 0.022
985
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.022
986
ORL011 Oral Cancer 60 0.022
987
STF001 Stiff-Person Syndrome 60 0.022
988
P THL005 Thalassemia 60 0.022
989
P OPT006 Optic Nerve Disease 60 0.022
990
P LKD001 Leukodystrophy 59 0.022
991
P SPN309 Spinocerebellar Ataxia 6 59 0.022
992
PRT058 Pure Autonomic Failure 59 0.022
993
PRN019 Perinatal Necrotizing Enterocolitis 59 0.022
994
P PRD006 Prader-Willi Syndrome 59 0.022
995
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.022
996
GRD007 Grade Iii Astrocytoma 59 0.022
997
AVN001 Avian Influenza 59 0.022
998
IRN001 Iron Deficiency Anemia 59 0.022
999
P NPH005 Nephronophthisis 59 0.022
1000
RNL024 Renal Glucosuria 58 0.022
1001
CRY005 Cryptococcosis 58 0.022
1002
ERY029 Erythermalgia, Primary 58 0.022
1003
FML063 Familial Glucocorticoid Deficiency 58 0.022
1004
c PRM005 Primary Hyperparathyroidism 58 0.022
1005
ERY003 Erythema Multiforme 58 0.022
1006
EYD002 Eye Disease 58 0.022
1007
DSS008 Disease of Mental Health 58 0.022
1008
P MMP001 Mumps 58 0.022
1009
APP015 Apparent Mineralocorticoid Excess 58 0.022
1010
EXT034 Extrinsic Allergic Alveolitis 58 0.022
1011
P OPT009 Optic Neuritis 57 0.022
1012
LYM021 Lymphadenitis 57 0.022
1013
P PRN023 Prion Disease 57 0.022
1014
APH001 Aphthous Stomatitis 57 0.022
1015
P URF003 Urofacial Syndrome 1 57 0.022
1016
P FBR017 Fibrosarcoma 56 0.022
1017
LMY014 Leiomyoma, Uterine 56 0.022
1018
ERY051 Erythroleukemia, Familial 56 0.022
1019
SFT003 Soft Tissue Sarcoma 56 0.022
1020
MTH009 Mouth Disease 56 0.022
1021
HMG005 Hemoglobinopathy 56 0.022
1022
INT030 Intracranial Aneurysm 56 0.022
1023
c PRG126 Progressive Familial Heart Block 55 0.022
1024
ADR008 Adrenal Adenoma 55 0.022
1025
NRG002 Neurogenic Bladder 55 0.022
1026
FDB001 Foodborne Botulism 55 0.022
1027
PLV003 Pelvic Inflammatory Disease 55 0.022
1028
P PTT006 Pituitary Adenoma 55 0.022
1029
P STR020 Strabismus 55 0.022
1030
P SBS003 Substance Abuse 55 0.022
1031
HDR002 Hidradenitis Suppurativa 55 0.022
1032
P ALP106 Alport Syndrome 1, X-Linked 55 0.022
1033
END040 Endogenous Depression 55 0.022
1034
HRY003 Hairy Cell Leukemia 55 0.022
1035
SYN007 Synovitis 54 0.022
1036
VGN023 Vaginitis 54 0.022
1037
P RST001 Restless Legs Syndrome 54 0.022
1038
P NLD001 Nail Disease 54 0.022
1039
P CYS039 Cystic Kidney Disease 54 0.022
1040
GST037 Gastroparesis 54 0.022
1041
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.022
1042
ANL018 Analbuminemia 54 0.022
1043
c SPN294 Spinocerebellar Ataxia 1 53 0.022
1044
RHM028 Rheumatic Heart Disease 53 0.022
1045
P INS002 in Situ Carcinoma 53 0.022
1046
KRT006 Keratoconjunctivitis 53 0.022
1047
P MNC007 Monocytic Leukemia 53 0.022
1048
CRH005 Crohn's Colitis 53 0.022
1049
BRN038 Bronchial Disease 53 0.022
1050
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.022
1051
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.022
1052
CLF001 Cleft Lip 53 0.022
1053
GSG001 Gas Gangrene 53 0.022
1054
PRN011 Pernicious Anemia 53 0.022
1055
P RTN022 Retinal Vein Occlusion 53 0.022
1056
PRP080 Peripheral Artery Disease 53 0.022
1057
c GLL024 Gallbladder Disease 1 53 0.022
1058
P INT068 Intestinal Disease 53 0.022
1059
c CNT035 Central Nervous System Disease 52 0.022
1060
CHR073 Choreatic Disease 52 0.022
1061
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.022
1062
P ACT105 Acute Mountain Sickness 52 0.022
1063
AGN003 Agenesis of the Corpus Callosum with Peripheral Neuropathy 52 0.022
1064
ART074 Aortic Dissection 52 0.022
1065
LMY002 Leiomyoma 52 0.022
1066
SPS003 Spastic Diplegia 51 0.022
1068
FCT001 Factor Viii Deficiency 51 0.022
1069
c ART120 Arthrogryposis, Distal, Type 3 51 0.022
1070
c PRM108 Primary Progressive Multiple Sclerosis 51 0.022
1071
P PRC012 Pericardial Effusion 51 0.022
1072
TNG007 Tongue Carcinoma 51 0.022
1073
P CHL066 Cholangitis 51 0.022
1074
PLR007 Pleural Empyema 50 0.022
1075