Search results for Potassium

2133 hits were found for Potassium

# Family MCID Name MIFTS Score
1
MYT030 Myotonia, Potassium-Aggravated 46 6.211
2
HYP005 Hypokalemia 55 5.751
3
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 4.183
4
OVR093 Overhydrated Hereditary Stomatocytosis 44 3.725
5
GTL001 Gitelman Syndrome 66 3.307
6
HYP052 Hyperkalemic Periodic Paralysis 59 2.014
7
P BRT004 Bartter Disease 55 1.965
8
KND001 Kindler Syndrome 63 1.935
9
SDM004 Sodium-Potassium-Atpase Activity of Red Cell 7 1.883
10
PTS020 Potassium Dichromate Allergic Contact Dermatitis 4 1.883
11
c OBS577 Obsolete: Channelopathy Due to a Voltage-Gated Potassium Channel Defect 3 1.876
12
c OBS578 Obsolete: Channelopathy Due to an Inwardly Rectifying Potassium Channel Defect 3 1.876
13
c OBS582 Obsolete: Channelopathy Due to a Calcium-Activated Potassium Channel Defect 3 1.876
14
c NRL029 Neurological Muscular Channelopathy Due to a Genetic Potassium Channel Defect 3 1.876
15
c OBS758 Obsolete: Autoimmune Neurological Channelopathy Due to a Potassium Channel Defect 2 1.876
16
c NRL037 Neurological Channelopathy of the Central Nervous System Due to a Genetic Potassium Channel Defect 2 1.876
17
NRM009 Normokalemic Periodic Paralysis 28 1.867
18
ALP077 Alpha-Methylacetoacetic Aciduria 56 1.857
19
c PRG143 Progressive Myoclonus Epilepsy 7 12 1.857
20
c EPL134 Epilepsy, Progressive Myoclonic 7 27 1.844
21
c HYP595 Hypertension, Essential 84 0.311
22
P KDN018 Kidney Disease 70 0.250
23
P LNG028 Long Qt Syndrome 65 0.236
24
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.212
25
P CRD119 Cardiac Arrest 67 0.208
26
HRW001 Hair Whorl 36 0.205
27
c ACT075 Acute Myocardial Infarction 56 0.204
28
ALL026 Allergic Hypersensitivity Disease 64 0.200
29
CNG034 Congestive Heart Failure 70 0.198
30
PRT037 Pertussis 65 0.189
31
c CHR684 Chronic Kidney Disease 66 0.183
32
HLX001 Helix Syndrome 47 0.180
33
MTB004 Metabolic Acidosis 50 0.177
34
ISC004 Ischemia 60 0.169
35
ANX004 Anoxia 42 0.169
36
P HRT032 Heart Disease 75 0.167
37
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.163
38
P PRD021 Periodic Paralysis 46 0.163
39
HYP266 Hypoxia 56 0.162
40
P ENC004 Encephalitis 61 0.161
41
P NRB001 Neuroblastoma 71 0.152
42
P MYC007 Myocardial Infarction 70 0.151
43
P DRR001 Diarrhea 57 0.150
44
CRD223 Cardiac Arrhythmia 60 0.147
45
48X005 48,xyyy 39 0.147
46
HYP056 Hypoglycemia 66 0.146
47
CRD132 Cardiac Conduction Defect 59 0.145
48
P SZR006 Seizure Disorder 58 0.144
49
END030 End Stage Renal Failure 58 0.144
50
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.144
51
VSL002 Visual Epilepsy 58 0.143
52
LMB024 Limbic Encephalitis 41 0.142
53
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.137
54
P HYP076 Hyperthyroidism 55 0.134
55
LVR012 Liver Cirrhosis 63 0.132
56
c MGR028 Migraine with or Without Aura 1 69 0.128
57
P GLM045 Glioma 63 0.128
58
GLL048 Glial Tumor 45 0.128
59
HYP066 Hyperglycemia 61 0.125
60
c GRV008 Graves Disease 1 55 0.124
61
P ATR011 Atrial Fibrillation 66 0.123
62
P HYP086 Hypothyroidism 68 0.122
63
P EPL164 Epilepsy 71 0.121
64
P ENC018 Encephalopathy 61 0.121
65
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.120
66
P EPS003 Episodic Ataxia 60 0.119
67
ATM095 Autoimmune Disease 61 0.114
68
P CYS018 Cystitis 59 0.112
69
ANG054 Angina Pectoris 66 0.110
70
HYP060 Hyperinsulinism 54 0.110
71
P LVR013 Liver Disease 68 0.109
72
OCL069 Ocular Motor Apraxia 51 0.109
73
PRS021 Prostatic Adenoma 51 0.108
74
PRS045 Prostatic Hypertrophy 52 0.107
75
PRS129 Prostatic Hyperplasia, Benign 49 0.107
76
P CRN018 Coronary Artery Anomaly 63 0.106
77
c BRN108 Branchiootic Syndrome 1 61 0.106
78
DRM006 Dermatitis 61 0.105
79
P INT143 Interstitial Cystitis 61 0.105
80
ADN018 Adenoma 58 0.105
81
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 57 0.105
82
c ACT071 Acute Kidney Failure 59 0.103
83
P DBT009 Diabetes Mellitus 64 0.102
84
P VSC007 Vascular Disease 63 0.102
85
DWN001 Down Syndrome 70 0.101
86
CRB039 Cerebrovascular Disease 69 0.101
87
c FML191 Familial Long Qt Syndrome 53 0.101
88
GTR002 Goiter 52 0.101
89
CRB004 Cerebral Artery Occlusion 44 0.101
90
STR067 Stroke, Ischemic 80 0.100
91
URM002 Uremia 49 0.100
92
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.098
93
P PLM037 Pulmonary Hypertension 68 0.098
94
P RNL007 Renal Tubular Acidosis 50 0.098
95
BNR002 Bone Resorption Disease 48 0.098
96
P GST053 Gastric Cancer 83 0.096
97
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.096
98
P TMP001 Temporal Lobe Epilepsy 50 0.096
99
CYS001 Cystic Fibrosis 80 0.093
100
P TRN020 Turner Syndrome 65 0.093
101
P DNT007 Dentin Sensitivity 35 0.093
102
TXC005 Toxic Shock Syndrome 61 0.092
103
ATR057 Atrioventricular Block 55 0.092
104
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.090
105
ADL002 Adult Syndrome 69 0.090
106
TTN003 Tetanus 64 0.090
107
PPT005 Peptic Ulcer Disease 58 0.090
108
P PYL005 Pyelonephritis 56 0.090
109
P CRD246 Cardiovascular System Disease 56 0.090
110
HYP014 Hyperuricemia 51 0.090
111
SPN186 Spinal Cord Injury 60 0.087
112
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.087
113
CHL014 Cholera 55 0.087
114
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.087
115
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.087
116
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.087
117
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.087
118
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.087
119
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.087
120
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.087
121
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.087
122
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.087
123
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.087
124
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.086
125
P MYP004 Myopathy 64 0.086
126
P CRN300 Coronary Heart Disease 1 63 0.086
127
c LNG047 Long Qt Syndrome 2 58 0.086
128
SPR010 Sporotrichosis 48 0.086
129
P THY054 Thyrotoxic Periodic Paralysis 47 0.086
130
P OST002 Osteoporosis 73 0.084
131
P ADN016 Adenocarcinoma 64 0.084
132
c PRC016 Pre-Eclampsia 63 0.084
133
c PNS012 Paine Syndrome 61 0.084
134
STT001 Status Epilepticus 59 0.084
135
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.084
136
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.084
137
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.083
138
P GRV001 Graves' Disease 55 0.083
139
P TRM003 Tremor 53 0.083
140
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.083
141
P MSC005 Muscular Dystrophy 66 0.081
142
c EPS042 Episodic Ataxia, Type 1 58 0.081
143
CNS004 Constipation 57 0.081
144
BRN004 Brain Edema 55 0.081
145
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.081
146
LWC001 Low Compliance Bladder 42 0.081
147
c SZR022 Seizures, Benign Familial Neonatal, 1 42 0.081
148
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.081
149
MYT011 Myotonia 35 0.081
150
CYN003 Cyanide Poisoning 24 0.081
151
c FML001 Familial Atrial Fibrillation 66 0.080
152
PRT036 Peritonitis 65 0.080
153
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.080
154
c ACT068 Acute Cystitis 63 0.080
155
CLT003 Colitis 62 0.080
156
P NRP001 Neuropathy 56 0.080
157
P PHC003 Pheochromocytoma 71 0.078
158
P CHR345 Chronic Pain 50 0.078
159
MLL001 Molluscum Contagiosum 49 0.078
160
BRN071 Brain Injury 49 0.078
161
ADR040 Adrenal Gland Pheochromocytoma 46 0.078
162
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.076
163
ULC004 Ulcerative Colitis 73 0.076
164
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.076
165
P MYS003 Myasthenia Gravis 68 0.076
166
ATH013 Atherosclerosis Susceptibility 66 0.076
167
HLC007 Helicobacter Pylori Infection 59 0.076
168
P GLM007 Glomerulonephritis 57 0.076
169
P DST107 Distal Renal Tubular Acidosis 41 0.076
170
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.076
171
ALC007 Alcohol Dependence 66 0.075
172
c FML036 Familial Periodic Paralysis 44 0.075
173
P BRS047 Breast Cancer 96 0.073
174
P ALZ034 Alzheimer Disease 88 0.073
175
GLB015 Glioblastoma Multiforme 75 0.073
176
c RHB024 Rhabdomyosarcoma 2 65 0.073
177
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.073
178
GLC003 Glucose Intolerance 54 0.073
179
ILS001 Ileus 51 0.073
180
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.073
181
P CLR023 Colorectal Cancer 98 0.071
182
P RSP003 Respiratory Failure 74 0.071
183
c HYP836 Hypercholesterolemia, Familial, 1 72 0.071
184
OTT002 Otitis Media 71 0.071
185
P NPH012 Nephrotic Syndrome 63 0.071
186
P PRD008 Periodontitis 62 0.071
187
CNT047 Contact Dermatitis 57 0.071
188
P DBT005 Diabetes Insipidus 55 0.071
189
PLM010 Pulmonary Edema 55 0.071
190
TRM010 Traumatic Brain Injury 53 0.071
191
ART140 Arteries, Anomalies of 53 0.071
192
NPH003 Nephrocalcinosis 51 0.071
193
PLP001 Pulpitis 48 0.071
194
P RNL015 Renal Hypertension 48 0.071
195
HYP189 Hypoadrenalism 37 0.071
196
P HYP120 Hypoaldosteronism 37 0.071
197
P BRG001 Brugada Syndrome 70 0.069
198
PLM001 Pulmonary Tuberculosis 70 0.069
199
P ESP024 Esophagitis 62 0.069
200
NTR005 Nutritional Deficiency Disease 61 0.069
201
P CTR002 Cataract 60 0.069
202
INS001 Insulinoma 60 0.069
203
DNT012 Dental Caries 51 0.069
204
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.068
205
ANX010 Anxiety 72 0.068
206
RCK004 Rickets 69 0.068
207
P PNM007 Pneumonia 68 0.068
208
P PSR002 Psoriasis 62 0.068
209
P HDC001 Headache 57 0.068
210
PST011 Pustulosis of Palm and Sole 52 0.068
211
HYP017 Hypophosphatemia 49 0.068
212
ATX019 Ataxia with Vitamin E Deficiency 48 0.068
213
P PSD003 Pseudohypoaldosteronism 45 0.068
214
ALL014 Allergic Encephalomyelitis 39 0.068
215
c ATM075 Autoimmune Encephalitis 38 0.068
216
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.068
217
c FML159 Familial Periodic Paralyses 17 0.068
218
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.066
219
HMN044 Human Immunodeficiency Virus Type 1 71 0.066
220
P LKM002 Leukemia 66 0.066
221
DPR016 Depression 63 0.066
222
P BND020 Bone Disease 59 0.066
223
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.066
224
AMN003 Amnestic Disorder 54 0.066
225
P LTR001 Lateral Sclerosis 53 0.066
226
PNG002 Pain Agnosia 51 0.066
227
P DDN001 Duodenal Ulcer 50 0.066
228
P BNG026 Benign Neonatal Seizures 48 0.066
229
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.066
230
P MLT020 Multiple Sclerosis 72 0.064
231
P AMY004 Amyloidosis 70 0.064
232
GST092 Gastroesophageal Reflux 65 0.064
233
IRN002 Iron Metabolism Disease 57 0.064
234
P RHN004 Rhinitis 57 0.064
235
P GST044 Gastritis 55 0.064
236
IMP005 Impotence 52 0.064
237
c SHR030 Short Qt Syndrome 48 0.064
238
MYC005 Myocardial Stunning 46 0.064
239
P MYC033 Myoclonus 46 0.064
240
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.062
241
c LKM071 Leukemia, Chronic Lymphocytic 79 0.062
242
AST005 Asthma 77 0.062
243
c ATR087 Atrial Standstill 1 74 0.062
244
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.062
245
P EXN002 Exanthem 57 0.062
246
SCH014 Schistosomiasis 56 0.062
247
P BPL003 Bipolar Disorder 56 0.062
248
INT007 Intermediate Coronary Syndrome 55 0.062
249
P LYM031 Lymphocytic Leukemia 55 0.062
250
PPL022 Papilloma 54 0.062
251
GLS018 Glass Syndrome 53 0.062
252
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 52 0.062
253
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 48 0.062
254
c MCR120 Microvascular Complications of Diabetes 7 47 0.062
255
P HMR005 Hemorrhoid 46 0.062
256
c MJR024 Major Affective Disorder 9 41 0.062
257
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.062
258
c MJR022 Major Affective Disorder 8 38 0.062
259
CHL079 Children's Interstitial Lung Disease 27 0.062
260
P LYM118 Lymphoma 68 0.060
261
OST159 Osteogenic Sarcoma 66 0.060
262
P MNN013 Meningitis 65 0.060
263
P THY023 Thymoma 65 0.060
264
GT001 Gout 63 0.060
265
P PLY014 Polycystic Kidney Disease 59 0.060
266
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.060
267
c THY107 Thymoma, Familial 54 0.060
268
GST023 Gastric Ulcer 53 0.060
269
P LCT001 Lactic Acidosis 51 0.060
270
P ECL001 Eclampsia 51 0.060
271
P RNV001 Renovascular Hypertension 49 0.060
272
SYN036 Syncope 45 0.060
273
HDN002 Head Injury 45 0.060
274
PPL052 Papillomatosis, Confluent and Reticulated 34 0.060
275
DFC004 Deficiency Anemia 75 0.057
276
P FRG001 Fragile X Syndrome 68 0.057
277
NRM005 Neuromuscular Disease 63 0.057
278
ANR007 Anorexia Nervosa 63 0.057
279
P SNS001 Sensorineural Hearing Loss 61 0.057
280
BCT022 Bacterial Infectious Disease 56 0.057
281
HRT012 Heart Valve Disease 53 0.057
282
c MCR113 Microvascular Complications of Diabetes 3 52 0.057
283
DRM011 Dermatophytosis 52 0.057
284
DMY004 Demyelinating Disease 52 0.057
285
47X002 47,xyy 49 0.057
286
ANR004 Anuria 46 0.057
287
PRM057 Paramyotonia Congenita of Von Eulenburg 46 0.057
288
P BNG032 Benign Mesothelioma 45 0.057
289
IDP073 Idiopathic Hypercalciuria 43 0.057
290
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 43 0.057
291
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.057
292
c MCR130 Microvascular Complications of Diabetes 6 41 0.057
293
c MCR133 Microvascular Complications of Diabetes 4 41 0.057
295
P LNG032 Lung Cancer 97 0.055
296
P RHM011 Rheumatoid Arthritis 80 0.055
297
P SCH015 Schizophrenia 75 0.055
298
CRH001 Crohn's Disease 74 0.055
299
SCK003 Sickle Cell Anemia 72 0.055
300
BRN024 Bronchitis 68 0.055
301
P ATS364 Autism 65 0.055
302
P HYP069 Hyperparathyroidism 62 0.055
303
P VSC011 Vasculitis 62 0.055
304
P EPL140 Epilepsy, Idiopathic Generalized 61 0.055
305
LNG099 Lung Disease 61 0.055
306
ACQ007 Acquired Immunodeficiency Syndrome 60 0.055
307
SQM006 Squamous Cell Carcinoma 60 0.055
308
GST045 Gastroenteritis 59 0.055
309
P ALC033 Alcohol Use Disorder 58 0.055
310
P PRP019 Peripheral Nervous System Disease 57 0.055
311
PRS047 Prostatitis 56 0.055
312
P INF037 Inflammatory Bowel Disease 56 0.055
313
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.055
314
FCL014 Focal Epilepsy 54 0.055
315
P MSC003 Muscular Atrophy 52 0.055
316
c VRL010 Viral Hepatitis 51 0.055
317
THR004 Thrombocytosis 51 0.055
318
P SCK005 Sickle Cell Disease 50 0.055
319
LYM019 Lymphosarcoma 47 0.055
320
P HYP733 Hypercalciuria, Absorptive, 2 46 0.055
321
HPT004 Hepatic Coma 43 0.055
322
c PRM038 Primary Agammaglobulinemia 43 0.055
323
HMP009 Haemophilus Influenzae 42 0.055
324
c CHR098 Chronic Pyelonephritis 35 0.055
325
c INT059 Internal Hemorrhoid 33 0.055
327
OST012 Osteoarthritis 78 0.053
328
P PRK057 Parkinson Disease, Late-Onset 76 0.053
329
ACR006 Aceruloplasminemia 73 0.053
330
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 0.053
331
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.053
332
P NTR004 Neutropenia 63 0.053
333
TRN015 Transient Cerebral Ischemia 62 0.053
334
HPT019 Hepatic Encephalopathy 60 0.053
335
THY029 Thyroid Carcinoma 59 0.053
336
P LDD007 Liddle Syndrome 1 59 0.053
337
P INT070 Intestinal Obstruction 58 0.053
338
TNS005 Tonsillitis 57 0.053
339
PLM031 Poliomyelitis 57 0.053
340
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 0.053
341
PHR003 Pharyngitis 56 0.053
342
AGN016 Aging 56 0.053
343
P AST007 Astrocytoma 50 0.053
344
HYP025 Hyperphosphatemia 47 0.053
345
SQM002 Squamous Cell Papilloma 42 0.053
346
SPS057 Spasticity 41 0.053
347
MST020 Mast Cell Activation Syndrome 27 0.053
348
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.050
349
IMM167 Immune Deficiency Disease 78 0.050
350
P GRF003 Graft-Versus-Host Disease 71 0.050
351
P SYS005 Systemic Scleroderma 70 0.050
352
CRT072 Creutzfeldt-Jakob Disease 69 0.050
353
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.050
354
P MCR115 Microvascular Complications of Diabetes 5 66 0.050
355
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.050
356
LPD008 Lipid Metabolism Disorder 62 0.050
357
P MVM001 Movement Disease 61 0.050
358
ERL001 Early Myoclonic Encephalopathy 61 0.050
359
P BCL017 B-Cell Lymphoma 58 0.050
360
P URT039 Urticaria 58 0.050
361
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.050
362
GST050 Gastrointestinal System Disease 56 0.050
363
DBT010 Diabetic Neuropathy 55 0.050
364
P ART021 Arteriosclerosis 54 0.050
365
c XNT010 Xanthinuria, Type I 50 0.050
366
STM007 Stomatitis 49 0.050
367
ECT026 Ectopic Pregnancy 49 0.050
368
INT067 Interstitial Nephritis 46 0.050
369
CRN019 Coronary Artery Vasospasm 46 0.050
370
PTT037 Pituitary Tumors 44 0.050
371
GNG003 Gingival Recession 44 0.050
372
ALD013 Aldosterone-Producing Adenoma 38 0.050
373
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.050
374
c SYS001 Systemic Lupus Erythematosus 86 0.048
375
INS024 Insulin-Like Growth Factor I 79 0.048
376
CNN003 Conn's Syndrome 79 0.048
377
P HNT016 Huntington Disease 71 0.048
378
c LNG044 Long Qt Syndrome 1 66 0.048
379
P DYS154 Dystonia 65 0.048
380
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.048
381
P END044 Endometriosis 62 0.048
382
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.048
383
FTT001 Fatty Liver Disease 61 0.048
384
CHL068 Cholestasis 60 0.048
385
P MYC008 Myocarditis 59 0.048
386
P SYP003 Syphilis 59 0.048
387
P END033 Endocarditis 57 0.048
388
RHM027 Rheumatic Disease 56 0.048
389
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.048
390
ALL010 Allergic Contact Dermatitis 55 0.048
391
PRT038 Protein-Energy Malnutrition 54 0.048
392
PRP016 Paraplegia 53 0.048
393
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 53 0.048
394
TLN003 Telangiectasis 51 0.048
395
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.048
396
P MGR003 Migraine with Aura 50 0.048
397
DYS015 Dysentery 50 0.048
398
P OVR082 Overgrowth Syndrome 50 0.048
399
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.048
400
NTR046 Neutrophil Migration 50 0.048
401
QDR001 Quadriplegia 48 0.048
402
CRD137 Cardiogenic Shock 48 0.048
403
TBR011 Tuberculous Meningitis 48 0.048
404
RNL077 Renal Fibrosis 47 0.048
405
SBC016 Subacute Delirium 44 0.048
406
CYT002 Cytokine Deficiency 44 0.048
407
CRB090 Cerebral Hypoxia 43 0.048
408
P HYP265 Hypotonia 42 0.048
409
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.048
410
HYP540 Hypertension, Diastolic 40 0.048
411
P FML187 Familial Hypertension 37 0.048
412
RRS014 Rare Surgical Neurologic Disease 32 0.048
413
P HPT023 Hepatocellular Carcinoma 100 0.045
414
c LKM061 Leukemia, Acute Myeloid 83 0.045
415
CRV035 Cervical Cancer 76 0.045
416
PRP027 Peripheral Vascular Disease 71 0.045
417
LYM133 Lymphoma, Hodgkin, Classic 69 0.045
418
P SLP006 Sleep Apnea 69 0.045
419
P MYC084 Mycobacterium Tuberculosis 1 68 0.045
420
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.045
421
DBT083 Diabetes Mellitus, Permanent Neonatal 64 0.045
422
OST017 Osteomyelitis 64 0.045
423
MDD011 Mood Disorder 62 0.045
424
P HMN010 Hemangioma 61 0.045
425
c HYP731 Hyperaldosteronism, Familial, Type I 60 0.045
426
DPH001 Diphtheria 60 0.045
427
c ACT073 Acute Leukemia 58 0.045
428
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.045
429
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.045
430
CMM005 Common Cold 56 0.045
431
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.045
432
P RNL017 Renal Oncocytoma 53 0.045
433
P THY032 Thyroiditis 53 0.045
434
THR013 Thoracic Outlet Syndrome 53 0.045
435
PYD002 Pyoderma 51 0.045
436
THY030 Thyroid Gland Disease 51 0.045
437
ENT011 Enterocolitis 50 0.045
438
c PYR010 Peyronie's Disease 50 0.045
439
P NNT009 Neonatal Diabetes Mellitus 50 0.045
440
P MYT002 Myotonic Dystrophy 49 0.045
441
c SPN311 Spinocerebellar Ataxia 13 49 0.045
442
PYL006 Pyloric Stenosis 48 0.045
443
c BNG006 Benign Familial Neonatal Epilepsy 47 0.045
444
CLS016 Clostridium Difficile Colitis 46 0.045
445
c BRT050 Bartter Syndrome, Type 2, Antenatal 45 0.045
446
c MLG068 Malignant Glioma 45 0.045
447
KWS001 Kwashiorkor 45 0.045
448
49X006 49, Xxxxy Syndrome 41 0.045
450
P PRS040 Prostate Cancer 97 0.042
451
P PNC035 Pancreatic Cancer 84 0.042
452
P BLD134 Bladder Cancer 78 0.042
453
LPT014 Leptin Deficiency or Dysfunction 73 0.042
454
P OCL013 Oculodentodigital Dysplasia 69 0.042
455
P INF038 Influenza 68 0.042
456
CRB037 Cerebral Palsy 68 0.042
457
c ATS007 Autism Spectrum Disorder 67 0.042
458
P MLG056 Malignant Hyperthermia 67 0.042
459
CNN005 Connective Tissue Disease 66 0.042
460
P CNJ013 Conjunctivitis 65 0.042
461
WLF001 Wolff-Parkinson-White Syndrome 65 0.042
462
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.042
463
P MTR014 Motor Neuron Disease 64 0.042
464
IRR002 Irritable Bowel Syndrome 63 0.042
465
MSC007 Muscle Hypertrophy 63 0.042
466
SKN016 Skin Disease 63 0.042
467
P HML002 Hemolytic Anemia 62 0.042
468
P HYP750 Hypertriglyceridemia, Familial 61 0.042
469
P MYL006 Myeloid Leukemia 60 0.042
470
P SLP005 Sleep Disorder 59 0.042
471
MNR012 Meniere Disease 57 0.042
472
MNT002 Mental Depression 57 0.042
473
P MYT023 Myotonia Congenita 55 0.042
474
P SCK002 Sick Sinus Syndrome 55 0.042
475
P PMP001 Pemphigus 55 0.042
476
P RTN016 Retinal Degeneration 53 0.042
477
MRG003 Marginal Zone B-Cell Lymphoma 53 0.042
478
P RCT021 Rectum Cancer 53 0.042
479
KRT009 Keratosis 53 0.042
480
PTH003 Pathologic Nystagmus 51 0.042
481
PPT001 Peptic Esophagitis 51 0.042
482
DYS073 Dysphagia 50 0.042
483
TRY001 Trypanosomiasis 50 0.042
484
PNN001 Panniculitis 49 0.042
485
ATN005 Autonomic Dysfunction 47 0.042
486
c BRT042 Bartter Syndrome, Type 3 46 0.042
487
ACT003 Acute Kidney Tubular Necrosis 45 0.042
488
P DYS021 Dysautonomia 39 0.042
489
VLK001 Volkmann Contracture 32 0.042
490
P PRD017 Periodic Paralyses 25 0.042
491
OBN001 Ouabain Resistance 18 0.042
492
P OVR042 Ovarian Cancer 89 0.039
493
MYL069 Myeloma, Multiple 85 0.039
494
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.039
495
P ART022 Arthritis 70 0.039
496
P HPT021 Hepatitis 67 0.039
497
P DMN002 Dementia 67 0.039
498
P NSP012 Nasopharyngeal Carcinoma 67 0.039
499
MNT001 Mantle Cell Lymphoma 66 0.039
500
P HYP098 Hypereosinophilic Syndrome 66 0.039
501
CHG001 Chagas Disease 66 0.039
502
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.039
503
c FNC043 Fanconi Anemia, Complementation Group E 62 0.039
504
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.039
505
P LPS004 Lupus Erythematosus 61 0.039
506
SDD001 Sudden Infant Death Syndrome 61 0.039
507
P PNC044 Pancreatitis 61 0.039
508
VRC005 Varicose Veins 60 0.039
509
ACN002 Acanthosis Nigricans 60 0.039
510
ETN001 Eating Disorder 59 0.039
511
c DWL002 Dowling-Degos Disease 1 58 0.039
512
P BNC003 Bone Cancer 57 0.039
513
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.039
514
CMR002 Coumarin Resistance 56 0.039
515
c SVR001 Severe Acute Respiratory Syndrome 55 0.039
516
P ANG015 Angioedema 54 0.039
517
P ESP035 Esophagitis, Eosinophilic, 1 54 0.039
518
AMN001 Amenorrhea 54 0.039
519
SNS003 Sensory Peripheral Neuropathy 53 0.039
520
INF034 Infective Endocarditis 52 0.039
521
NNL006 Non-Alcoholic Steatohepatitis 51 0.039
522
CRN030 Coronary Stenosis 50 0.039
523
ENT004 Enthesopathy 48 0.039
524
WTH001 Withdrawal Disorder 48 0.039
525
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.039
526
ASP007 Aspiration Pneumonia 48 0.039
527
RTN020 Retinal Vascular Disease 48 0.039
528
c MLG069 Malignant Hypertension 47 0.039
529
RTN023 Retinitis 46 0.039
530
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.039
531
BRN032 Brain Glioma 43 0.039
532
c BRT052 Bartter Syndrome, Type 1, Antenatal 43 0.039
533
NRR001 Neuroretinitis 43 0.039
534
TRP009 Triple X Syndrome 42 0.039
535
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 42 0.039
536
SNL007 Senile Cataract 42 0.039
537
MDL009 Medullary Sponge Kidney 42 0.039
538
PRM020 Premenstrual Tension 39 0.039
539
c PSD092 Pseudohypoaldosteronism, Type Iie 38 0.039
540
c THY084 Thyrotoxic Periodic Paralysis 1 35 0.039
542
c HYP438 Hyperaldosteronism, Familial, Type Iii 32 0.039
543
ADG002 Audiogenic Seizures 26 0.039
544
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.039
545
URT049 Urate Oxidase, Pseudogene 25 0.039
546
PRN068 Paraneoplastic Limbic Encephalitis 21 0.039
547
CNV009 Convulsions Benign Familial Neonatal Dominant Form 17 0.039
548
c DLT002 Dilated Cardiomyopathy 79 0.036
549
P LNG064 Lung Cancer Susceptibility 3 77 0.036
550
P RTN008 Retinitis Pigmentosa 77 0.036
551
END057 Endometrial Cancer 74 0.036
552
BRN028 Brain Cancer 73 0.036
553
MSC157 Muscular Dystrophy, Duchenne Type 71 0.036
554
P SRC025 Sarcoidosis 1 70 0.036
555
WLS001 Wilson Disease 70 0.036
556
GST040 Gastric Adenocarcinoma 70 0.036
557
MLN008 Melanoma 69 0.036
558
KRT019 Keratitis, Hereditary 67 0.036
559
BRK010 Burkitt Lymphoma 67 0.036
560
ALL003 Allergic Rhinitis 67 0.036
561
P LPR021 Leprosy 3 67 0.036
562
PSY004 Psychotic Disorder 67 0.036
563
P FLL037 Follicular Lymphoma 66 0.036
564
c MCR129 Microvascular Complications of Diabetes 1 66 0.036
565
SRC014 Sarcoma 65 0.036
566
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.036
567
c ART101 Aortic Valve Disease 2 63 0.036
568
IDP011 Idiopathic Interstitial Pneumonia 63 0.036
569
P ANR048 Aniridia 1 63 0.036
570
P ADL010 Adult Respiratory Distress Syndrome 63 0.036
571
c EPS035 Episodic Ataxia, Type 2 63 0.036
572
c HPT001 Hepatitis C 63 0.036
573
c HPT003 Hepatitis a 63 0.036
574
P PLM036 Pulmonary Fibrosis 61 0.036
575
APP008 Appendicitis 60 0.036
576
c VSC019 Vesicoureteral Reflux 1 59 0.036
577
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.036
578
GNG013 Gingivitis 59 0.036
579
c ACT027 Acute Pancreatitis 59 0.036
580
HYD002 Hydronephrosis 59 0.036
581
CHL123 Chlamydia 59 0.036
582
BRN002 Bronchiolitis 59 0.036
583
CHL067 Cholecystitis 58 0.036
584
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.036
585
BNG009 Benign Epilepsy with Centrotemporal Spikes 58 0.036
586
P CND004 Candidiasis 57 0.036
587
P INF032 Infertility 57 0.036
588
VSC002 Vascular Dementia 57 0.036
589
THR024 Thrombosis 56 0.036
590
ANG005 Anogenital Venereal Wart 56 0.036
591
c INT072 Intestinal Pseudo-Obstruction 56 0.036
592
CHR177 Chromophobe Renal Cell Carcinoma 56 0.036
593
ALL006 Allergic Asthma 56 0.036
594
LYM040 Lymphoblastic Lymphoma 54 0.036
595
INT075 Intracranial Hypertension 53 0.036
596
c LNG048 Long Qt Syndrome 3 52 0.036
597
MCN017 Meconium Ileus 52 0.036
598
MCR141 Mucormycosis 51 0.036
599
SPL004 Splenic Marginal Zone Lymphoma 51 0.036
600
SPN035 Spindle Cell Sarcoma 51 0.036
601
c ALM001 Al Amyloidosis 50 0.036
602
HYP781 Hypoascorbemia 50 0.036
603
ALL009 Allergic Conjunctivitis 50 0.036
604
VLV047 Volvulus of Midgut 50 0.036
605
c SVR005 Severe Pre-Eclampsia 49 0.036
606
VCC001 Vaccinia 49 0.036
607
c FLL041 Follicular Lymphoma 1 49 0.036
608
KRT002 Keratomalacia 48 0.036
609
c PRM093 Premature Ovarian Failure 7 47 0.036
610
c LRG017 Large Intestine Cancer 47 0.036
611
PLS025 Plasmablastic Lymphoma 47 0.036
612
URT010 Ureteral Obstruction 46 0.036
613
P MTH007 Methemoglobinemia 46 0.036
614
INT071 Intestinal Perforation 45 0.036
615
PRL008 Paralytic Ileus 44 0.036
616
DVR002 Diverticulitis 44 0.036
617
c PCH010 Pachyonychia Congenita 3 43 0.036
618
ORL015 Oral Squamous Cell Carcinoma 43 0.036
619
c FML294 Familial Short Qt Syndrome 43 0.036
620
IDP033 Idiopathic Edema 43 0.036
621
PRS063 Paresthesia 43 0.036
622
c MCR112 Microvascular Complications of Diabetes 2 41 0.036
623
c CNG027 Congenital Hemolytic Anemia 40 0.036
624
ENT001 Enterocele 39 0.036
625
ATM052 Autoimmune Disease 1 37 0.036
626
CHR178 Chromosomal Triplication 35 0.036
627
HNS001 Hansen's Disease 34 0.036
628
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.036
629
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.036
630
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.036
631
CYT018 Cytochrome P450 2d6 Variant 27 0.036
632
MTH071 Methane Production 26 0.036
633
c BRT024 Bartter Syndrome Type 4 25 0.036
634
CRM010 Cramp-Fasciculation Syndrome 15 0.036
635
KCN019 Kcnk9 Imprinting Syndrome 14 0.036
636
ESP021 Esophageal Cancer 90 0.032
637
NRL016 Neural Tube Defects 82 0.032
638
P NRF023 Neurofibromatosis, Type Ii 76 0.032
639
GST019 Gastrointestinal Stromal Tumor 76 0.032
640
c THR092 Thrombophilia Due to Thrombin Defect 73 0.032
641
ACR007 Acromegaly 71 0.032
642
c HPT073 Hepatitis C Virus 70 0.032
643
MYL009 Myelodysplastic Syndrome 70 0.032
644
P LKM062 Leukemia, Acute Lymphoblastic 68 0.032
645
P MJR001 Major Depressive Disorder 68 0.032
646
P ESS003 Essential Thrombocythemia 67 0.032
647
P SKN015 Skin Carcinoma 67 0.032
648
P DRM053 Dermatitis, Atopic 66 0.032
649
P MTR004 Maturity-Onset Diabetes of the Young 66 0.032
650
LPT001 Leptospirosis 66 0.032
651
MYC006 Mycosis Fungoides 66 0.032
652
P NRV007 Nervous System Disease 66 0.032
653
P HRP006 Herpes Simplex 65 0.032
654
MYL031 Myeloproliferative Neoplasm 65 0.032
655
APN008 Apnea, Obstructive Sleep 65 0.032
656
CLN015 Colon Adenocarcinoma 63 0.032
657
TYP007 Typhoid Fever 63 0.032
658
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.032
659
P ART023 Arthropathy 62 0.032
660
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.032
661
P PRM006 Primary Biliary Cirrhosis 61 0.032
662
OST003 Osteonecrosis 61 0.032
663
VRL011 Viral Infectious Disease 61 0.032
664
RHM001 Rheumatic Fever 61 0.032
665
PRT013 Portal Hypertension 60 0.032
666
YLL002 Yellow Fever 60 0.032
667
WST001 West Syndrome 60 0.032
668
P GLL022 Guillain-Barre Syndrome 59 0.032
669
SPP011 Suppression of Tumorigenicity 12 59 0.032
670
c DNG003 Dengue Disease 59 0.032
671
PLM033 Pulmonary Embolism 59 0.032
672
FBR047 Fibromyalgia 59 0.032
673
P BRS044 Breast Adenocarcinoma 59 0.032
674
ANR040 Aneurysm 58 0.032
675
URN010 Urinary Tract Obstruction 57 0.032
676
BLR008 Bilirubin Metabolic Disorder 57 0.032
677
GST033 Gestational Diabetes 57 0.032
678
P HYP024 Hypoparathyroidism 55 0.032
679
PRP030 Purpura 55 0.032
680
c FML035 Familial Hyperlipidemia 55 0.032
681
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.032
682
RSC001 Rosacea 55 0.032
683
P MYP006 Myopia 55 0.032
684
PYD001 Pyoderma Gangrenosum 54 0.032
685
P DRM007 Dermatitis Herpetiformis 54 0.032
686
P SLM003 Salmonellosis 54 0.032
687
c PRD040 Periodontitis, Chronic 54 0.032
688
c FML023 Familial Hemiplegic Migraine 54 0.032
689
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.032
690
OCL006 Ocular Hypertension 53 0.032
691
MST005 Mastitis 53 0.032
692
P RTN018 Retinal Disease 52 0.032
693
ACR041 Acromelic Frontonasal Dysostosis 52 0.032
694
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.032
695
P ACT008 Actinic Keratosis 52 0.032
696
PLS009 Plasma Cell Neoplasm 51 0.032
697
ONC002 Onchocerciasis 51 0.032
698
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.032
699
NRM004 Neuroma 51 0.032
700
c SCN007 Secondary Hyperparathyroidism 50 0.032
701
HPT014 Hepatorenal Syndrome 50 0.032
702
c INF145 Infantile Liver Failure Syndrome 1 50 0.032
703
CHL004 Cholelithiasis 49 0.032
704
PLC008 Placenta Disease 49 0.032
705
LRN003 Learning Disability 49 0.032
706
P OPN001 Open-Angle Glaucoma 49 0.032
707
SNT005 Sinoatrial Node Disease 49 0.032
708
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.032
709
c BCT013 Bacterial Pneumonia 47 0.032
710
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.032
711
LCK001 Locked-in Syndrome 46 0.032
712
CYN002 Cyanosis, Transient Neonatal 45 0.032
713
GRN007 Granuloma Annulare 45 0.032
714
P HMP006 Hemiplegic Migraine 44 0.032
715
NWC001 Newcastle Disease 44 0.032
716
CHR031 Chromoblastomycosis 44 0.032
717
GRN017 Granulocytopenia 44 0.032
718
PNC085 Penicillin Allergy 44 0.032
719
ATN004 Autonomic Neuropathy 44 0.032
720
P BCT020 Bacteremia 2 44 0.032
721
ESN004 Eosinophilic Gastritis 44 0.032
722
P MYG005 Myoglobinuria 43 0.032
723
BCK006 Back Pain 42 0.032
724
RDN001 Reading Disorder 40 0.032
725
FNG016 Fungal Keratitis 40 0.032
726
P ANT061 Antenatal Bartter Syndrome 40 0.032
727
LKP003 Leukoplakia 39 0.032
728
WLL004 Wallerian Degeneration 39 0.032
729
AMN006 Aminoaciduria 38 0.032
730
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.032
731
HRN029 Hearing Loss, Noise-Induced 37 0.032
732
P MXL015 Maxillary Sinusitis 37 0.032
733
SCR003 Secretory Diarrhea 36 0.032
734
c DRM040 Dermatitis Herpetiformis, Familial 35 0.032
735
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.032
736
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 34 0.032
737
c PRG106 Progressive Muscular Dystrophy 33 0.032
738
c THY083 Thyrotoxic Periodic Paralysis 2 33 0.032
739
P VSC018 Visceral Steatosis 33 0.032
740
PLY150 Polykaryocytosis Inducer 31 0.032
741
SLC024 Slc4a1-Associated Distal Renal Tubular Acidosis 19 0.032
742
P ATX030 Ataxia-Telangiectasia 83 0.028
743
P GLM040 Glioma Susceptibility 1 81 0.028
744
P MDL005 Medulloblastoma 77 0.028
745
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.028
746
SVR004 Severe Combined Immunodeficiency 73 0.028
747
c SPN225 Spondyloarthropathy 1 73 0.028
748
c LKM063 Leukemia, Chronic Myeloid 71 0.028
749
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.028
750
P TBR001 Tuberous Sclerosis 70 0.028
751
P TTR001 Tetralogy of Fallot 69 0.028
752
PLY001 Polycythemia Vera 69 0.028
753
ART016 Aortic Aneurysm 68 0.028
754
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.028
755
P THR014 Thrombocytopenia 68 0.028
756
PNC129 Pancreatic Adenocarcinoma 67 0.028
757
MYL005 Myelofibrosis 67 0.028
758
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.028
759
P ANG001 Angelman Syndrome 67 0.028
760
GLL008 Gilles De La Tourette Syndrome 66 0.028
761
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.028
762
P HYD006 Hydrocephalus 65 0.028
763
c SML038 Small Cell Cancer of the Lung 65 0.028
764
P LPS002 Liposarcoma 65 0.028
765
BRR014 Barrett Esophagus 64 0.028
766
P CHR071 Charcot-Marie-Tooth Disease 64 0.028
767
c DYS056 Dystonia 12 64 0.028
768
KHL003 Kohlschutter-Tonz Syndrome 64 0.028
769
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.028
770
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.028
771
P MCH002 Machado-Joseph Disease 63 0.028
772
PPL049 Papillon-Lefevre Syndrome 63 0.028
773
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.028
774
P RHB003 Rhabdomyosarcoma 62 0.028
775
P BCK002 Beckwith-Wiedemann Syndrome 62 0.028
776
TMT001 Timothy Syndrome 62 0.028
777
HMT002 Hematologic Cancer 62 0.028
778
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.028
779
CHR066 Chronic Fatigue Syndrome 61 0.028
780
INT002 Intermittent Claudication 61 0.028
781
P ANP001 Anaplastic Large Cell Lymphoma 61 0.028
782
LYM012 Lymphoplasmacytic Lymphoma 61 0.028
783
MSL001 Measles 61 0.028
784
SZR001 Sezary's Disease 60 0.028
785
ING001 Inguinal Hernia 60 0.028
786
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.028
787
TRG002 Trigeminal Neuralgia 60 0.028
788
CYS010 Cystinosis 60 0.028
789
PNM010 Pneumothorax, Primary Spontaneous 60 0.028
790
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.028
791
CHR072 Chordoma 59 0.028
792
INT066 Interstitial Lung Disease 59 0.028
793
P BRN022 Bronchiectasis 59 0.028
794
c HPT016 Hepatitis B 59 0.028
795
P CHR285 Chronic Myelomonocytic Leukemia 59 0.028
796
P PLV020 Pelvic Organ Prolapse 59 0.028
797
c SPN301 Spinocerebellar Ataxia 2 59 0.028
798
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.028
799
PST028 Post-Traumatic Stress Disorder 58 0.028
800
P GLL020 Gallbladder Disease 58 0.028
801
NWB001 Newborn Respiratory Distress Syndrome 58 0.028
802
BLM002 Bulimia Nervosa 57 0.028
803
P PLY041 Polymyositis 57 0.028
804
c MST023 Mesothelioma, Malignant 57 0.028
805
c ADL017 Adult T-Cell Leukemia 57 0.028
806
ADN027 Adenomyosis 57 0.028
807
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.028
808
PLS011 Plasmacytoma 56 0.028
809
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.028
810
P MLN007 Male Infertility 56 0.028
811
PNM008 Pneumothorax 56 0.028
812
P PLY019 Polyneuropathy 56 0.028
813
P PNM006 Pneumoconiosis 55 0.028
814
P PLY018 Polycythemia 55 0.028
815
c BCT007 Bacterial Meningitis 55 0.028
816
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.028
817
NRN004 Neuroendocrine Tumor 55 0.028
818
CLL003 Cellulitis 54 0.028
819
HMP005 Hemiplegia 54 0.028
820
CRT017 Cartilage Disease 54 0.028
821
P TCD001 Tic Disorder 54 0.028
822
P CYS039 Cystic Kidney Disease 54 0.028
823
LST001 Listeriosis 54 0.028
824
PRC013 Pericarditis 54 0.028
825
NRT004 Neuritis 53 0.028
826
RHM028 Rheumatic Heart Disease 53 0.028
827
ALC009 Alcoholic Liver Cirrhosis 53 0.028
828
NRT001 Neurotic Disorder 52 0.028
829
P HMR003 Hemorrhagic Disease 52 0.028
830
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.028
831
TXC002 Toxic Encephalopathy 52 0.028
832
c PRM012 Primary Polycythemia 52 0.028
833
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.028
834
P HMP007 Hemophilia 51 0.028
835
THR016 Thrombophlebitis 51 0.028
836
c ACT134 Acute Liver Failure 51 0.028
837
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.028
838
P CNT056 Cantu Syndrome 51 0.028
839
AZS001 Azoospermia 50 0.028
840
HYP081 Hypolipoproteinemia 50 0.028
841
P HYP077 Hypertrichosis 50 0.028
842
ACH005 Achalasia 50 0.028
843
MCR004 Macroglobulinemia 50 0.028
844
OPT003 Opiate Dependence 50 0.028
845
P OTS001 Otosclerosis 50 0.028
846
P CTN015 Cutaneous T Cell Lymphoma 49 0.028
847
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.028
848
LFT001 Left Bundle Branch Hemiblock 49 0.028
849
c BPL002 Bipolar I Disorder 49 0.028
850
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.028
851
c DYS119 Dystonia 9 49 0.028
852
GYN001 Gynecomastia 49 0.028
853
ATY042 Atypical Chronic Myeloid Leukemia 49 0.028
854
c THR090 Thrombocythemia 1 49 0.028
855
CLN045 Colonic Benign Neoplasm 49 0.028
856
URT001 Urethritis 48 0.028
857
BLD044 Bladder Disease 48 0.028
858
BCT004 Bacteriuria 48 0.028
859
P CMP008 Compartment Syndrome 48 0.028
860
c ACT150 Acute Adrenal Insufficiency 48 0.028
861
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.028
862
ATS010 Autosomal Recessive Disease 48 0.028
863
CHR563 Chronic Eosinophilic Leukemia 48 0.028
864
CCN002 Cocaine Abuse 48 0.028
865
P MRC003 Mercury Poisoning 48 0.028
866
INT054 Intraocular Lymphoma 48 0.028
867
ANT018 Anthracosis 48 0.028
868
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.028
869
THY128 Thyroid Tumor 47 0.028
870
P TCL004 T-Cell Leukemia 47 0.028
871
P CRC039 Coarctation of Aorta 47 0.028
872
TNP001 Tinea Pedis 47 0.028
873
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.028
874
P VTR007 Vitreoretinopathy 46 0.028
875
PRP017 Periapical Periodontitis 46 0.028
876
EXT010 Extramedullary Plasmacytoma 45 0.028
877
P OVR046 Ovarian Cyst 45 0.028
878
LYM051 Lymphomatoid Granulomatosis 45 0.028
879
MYX004 Myxedema 44 0.028
880
ACT029 Acute Interstitial Pneumonia 44 0.028
881
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.028
882
MNG006 Monogenic Diabetes 44 0.028
883
CRT015 Carotid Artery Occlusion 44 0.028
884
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.028
885
CNT017 Central Nervous System Origin Vertigo 44 0.028
886
DMP001 Dumping Syndrome 44 0.028
887
P MJR007 Major Affective Disorder 1 43 0.028
888
BNM001 Bone Marrow Cancer 43 0.028
889
c HYP272 Hypercholesterolemia, Familial, 3 43 0.028
890
MRS001 Marasmus 43 0.028
891
ASP008 Aspiration Pneumonitis 42 0.028
892
MYF002 Myofascial Pain Syndrome 42 0.028
893
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.028
894
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.028
895
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.028
896
CHR286 Chronic Neutrophilic Leukemia 41 0.028
897
P CND005 Cone Dystrophy 41 0.028
898
GST020 Gastric Antral Vascular Ectasia 41 0.028
899
RST023 Resting Heart Rate, Variation in 41 0.028
900
P FML156 Familial Hyperaldosteronism 41 0.028
901
c LNG053 Long Qt Syndrome 9 41 0.028
902
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.028
903
VLV042 Vulvar Vestibulitis Syndrome 40 0.028
904
CRY019 Cryohydrocytosis 40 0.028
905
ANG049 Angioedema Induced by Ace Inhibitors 40 0.028
906
BRK002 Birk-Barel Syndrome 39 0.028
908
CRV045 Cervical Intraepithelial Neoplasia 39 0.028
909
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.028
910
VLL006 Villous Adenoma 38 0.028
911
SCR011 Scrapie 38 0.028
912
P PST059 Pustular Psoriasis 38 0.028
913
P CRB088 Cerebral Atrophy 38 0.028
914
TNC002 Tinea Capitis 38 0.028
915
URT004 Urethral Syndrome 38 0.028
916
ATX010 Ataxia Neuropathy Spectrum 38 0.028
917
MYT003 Myotonic Disease 37 0.028
918
DRM009 Dermatomycosis 36 0.028
919
ABD010 Abdominal Wall Defect 35 0.028
920
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.028
921
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.028
922
PST010 Pasteurellosis 33 0.028
923
BNN005 Bunion 33 0.028
924
c PSD090 Pseudohypoaldosteronism, Type Iia 33 0.028
925
CLN006 Colonic Pseudo-Obstruction 33 0.028
926
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.028
927
HND015 Hand Skill, Relative 33 0.028
928
CND006 Candida Glabrata 32 0.028
929
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.028
930
ACT064 Acute Necrotizing Encephalitis 32 0.028
931
P ATS382 Autosomal Dominant Tubulointerstitial Kidney Disease 31 0.028
932
INF021 Infant Gynecomastia 31 0.028
933
FNT004 Fainting 31 0.028
934
c PSD093 Pseudohypoaldosteronism, Type Iid 30 0.028
935
PST092 Posttransplant Acute Limbic Encephalitis 29 0.028
936
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.028
937
c LNG052 Long Qt Syndrome 8 26 0.028
938
c HRD219 Hereditary Distal Renal Tubular Acidosis 26 0.028
939
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.028
940
BLD137 Blood Group--Ahonen 19 0.028
941
MYP026 Myopathy - Thyrotoxic 17 0.028
942
DGT004 Digitalis Poisoning 14 0.028
943
HRD103 Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum 14 0.028
944
NNP018 Non-Paraneoplastic Limbic Encephalitis 12 0.028
945
P OBS151 Obsolete: Channelopathy 8 0.028
947
P RTT002 Rett Syndrome 80 0.023
948
MLR004 Malaria 80 0.023
949
c TBR025 Tuberous Sclerosis 1 76 0.023
950
MRF001 Marfan Syndrome 75 0.023
951
P APL001 Aplastic Anemia 74 0.023
952
ADR007 Adrenoleukodystrophy 74 0.023
953
P FML018 Familial Mediterranean Fever 72 0.023
954
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.023
955
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.023
956
EWN003 Ewing Sarcoma 68 0.023
957
P ALP004 Alport Syndrome 68 0.023
958
c INF071 Inflammatory Bowel Disease 1 68 0.023
959
SKN019 Skin Melanoma 67 0.023
960
GRG001 Greig Cephalopolysyndactyly Syndrome 67 0.023
961
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.023
962
FCT007 Factor Vii Deficiency 66 0.023
963
c MYT021 Myotonic Dystrophy 1 66 0.023
964
c HMP029 Hemophilia a 65 0.023
965
LYS012 Lysosomal Acid Lipase Deficiency 64 0.023
966
CLR108 Colorectal Adenoma 64 0.023
967
ART002 Arts Syndrome 63 0.023
968
ACT119 Acute Promyelocytic Leukemia 63 0.023
969
c SCL052 Scleroderma, Familial Progressive 62 0.023
970
CYS013 Cystinuria 62 0.023
971
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.023
972
WLL001 Williams-Beuren Syndrome 62 0.023
973
c GLC092 Glaucoma, Primary Open Angle 62 0.023
974
HYP780 Hypoadrenocorticism, Familial 62 0.023
975
ALC006 Alcoholic Hepatitis 61 0.023
976
HYD038 Hydrops Fetalis, Nonimmune 61 0.023
977
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 61 0.023
978
P DRM010 Dermatomyositis 61 0.023
979
P KDN017 Kidney Cancer 61 0.023
980
P CHL002 Childhood Absence Epilepsy 60 0.023
981
P NRM001 Neuromyelitis Optica 60 0.023
982
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.023
983
P VNT002 Ventricular Septal Defect 60 0.023
984
RTN017 Retinal Detachment 60 0.023
985
STF001 Stiff-Person Syndrome 60 0.023
986
ORL011 Oral Cancer 60 0.023
987
HRP004 Herpes Zoster 60 0.023
988
P THL005 Thalassemia 60 0.023
989
P SPN309 Spinocerebellar Ataxia 6 59 0.023
990
PRT058 Pure Autonomic Failure 59 0.023
991
P LKD001 Leukodystrophy 59 0.023
992
P TRC086 Trichohepatoenteric Syndrome 1 59 0.023
993
GRD007 Grade Iii Astrocytoma 59 0.023
994
IRN001 Iron Deficiency Anemia 58 0.023
995
CRY005 Cryptococcosis 58 0.023
996
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.023
997
P NPH005 Nephronophthisis 58 0.023
998
EYD002 Eye Disease 58 0.023
999
ERY029 Erythermalgia, Primary 58 0.023
1000
ANG020 Angiosarcoma 58 0.023
1001
c PRG126 Progressive Familial Heart Block 58 0.023
1002
EXT034 Extrinsic Allergic Alveolitis 58 0.023
1003
c PRM005 Primary Hyperparathyroidism 58 0.023
1004
LYM021 Lymphadenitis 58 0.023
1005
P OPT006 Optic Nerve Disease 57 0.023
1006
ERY003 Erythema Multiforme 57 0.023
1007
P MMP001 Mumps 57 0.023
1008
RNL024 Renal Glucosuria 57 0.023
1009
BRN056 Bronchopulmonary Dysplasia 57 0.023
1010
DSS008 Disease of Mental Health 57 0.023
1011
P PRN023 Prion Disease 57 0.023
1012
c MYT020 Myotonic Dystrophy 2 57 0.023
1013
APH001 Aphthous Stomatitis 57 0.023
1014
P STR020 Strabismus 56 0.023
1015
ERY051 Erythroleukemia, Familial 56 0.023
1016
P FBR017 Fibrosarcoma 56 0.023
1017
P OPT009 Optic Neuritis 56 0.023
1018
SFT003 Soft Tissue Sarcoma 56 0.023
1019
LMY014 Leiomyoma, Uterine 56 0.023
1020
AVN001 Avian Influenza 56 0.023
1021
FDB001 Foodborne Botulism 56 0.023
1022
MTH009 Mouth Disease 56 0.023
1023
ADR008 Adrenal Adenoma 56 0.023
1024
INT030 Intracranial Aneurysm 56 0.023
1025
HMG005 Hemoglobinopathy 55 0.023
1026
SYN007 Synovitis 55 0.023
1027
HRY003 Hairy Cell Leukemia 55 0.023
1028
FCT001 Factor Viii Deficiency 55 0.023
1029
TNG003 Tongue Cancer 55 0.023
1030
VGN023 Vaginitis 55 0.023
1031
P SBS003 Substance Abuse 54 0.023
1032
NRG002 Neurogenic Bladder 54 0.023
1033
P PTT006 Pituitary Adenoma 54 0.023
1034
END040 Endogenous Depression 54 0.023
1035
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 54 0.023
1036
c CNT035 Central Nervous System Disease 54 0.023
1037
GST037 Gastroparesis 53 0.023
1038
HDR002 Hidradenitis Suppurativa 53 0.023
1039
BRN038 Bronchial Disease 53 0.023
1040
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.023
1041
P LYM025 Lymphedema 53 0.023
1042
P ART018 Aortic Valve Insufficiency 53 0.023
1043
KRT006 Keratoconjunctivitis 53 0.023
1044
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 53 0.023
1045
CLF001 Cleft Lip 53 0.023
1046
PRP080 Peripheral Artery Disease 53 0.023
1047
CRH005 Crohn's Colitis 52 0.023
1048
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.023
1049
c SPN294 Spinocerebellar Ataxia 1 52 0.023
1050
PRN011 Pernicious Anemia 52 0.023
1051
P ACT105 Acute Mountain Sickness 52 0.023
1052
c GLL024 Gallbladder Disease 1 52 0.023
1053
CHR073 Choreatic Disease 52 0.023
1054
P RTN022 Retinal Vein Occlusion 52 0.023
1055
AGN003 Agenesis of the Corpus Callosum with Peripheral Neuropathy 52 0.023
1057
FML063 Familial Glucocorticoid Deficiency 51 0.023
1058
c PRM108 Primary Progressive Multiple Sclerosis 51 0.023
1059
P PRC012 Pericardial Effusion 51 0.023
1060
GSG001 Gas Gangrene 50 0.023
1061
c BRG005 Brugada Syndrome 1 50 0.023
1062
HRT011 Heart Septal Defect 50 0.023
1063
RTN003 Retinal Ischemia 50 0.023
1064
ADT003 Auditory System Disease 50 0.023
1065
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.023
1066
BRX001 Bruxism 50 0.023
1067
P FNC004 Fanconi Syndrome 50 0.023
1068
SPS003 Spastic Diplegia 50 0.023
1069
SLD003 Sialadenitis 50 0.023
1070
LMY002 Leiomyoma 50 0.023
1071
P CHL066 Cholangitis 50 0.023
1072
VPM001 Vipoma 50 0.023
1073
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.023
1074
c MLG054 Malignant Histiocytosis 50 0.023