Search results for sodium

3326 hits were found for sodium

# Family MCID Name MIFTS Score
1
DRR017 Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies 33 8.072
2
DRR013 Diarrhea 8, Secretory Sodium, Congenital 25 5.716
3
SDM005 Sodium Serum Level Quantitative Trait Locus 1 11 4.502
4
MYT030 Myotonia, Potassium-Aggravated 45 3.557
5
OVR093 Overhydrated Hereditary Stomatocytosis 40 3.510
7
SDM004 Sodium-Potassium-Atpase Activity of Red Cell 6 2.868
8
SDM006 Sodium Aurothiomalate Allergy 4 2.863
9
HYP052 Hyperkalemic Periodic Paralysis 59 2.205
10
P NRL027 Neurological Muscular Channelopathy Due to a Genetic Sodium Channel Defect 3 2.031
11
c OBS581 Obsolete: Channelopathy Due to a Voltage-Gated Sodium Channel Defect 3 2.031
12
c OBS586 Obsolete: Channelopathy Due to an Epithelial Sodium Channel Defect 3 2.031
13
c NRL035 Neurological Channelopathy of the Central Nervous System Due to a Genetic Sodium Channel Defect 2 2.031
14
c HYP595 Hypertension, Essential 87 0.417
15
CLT003 Colitis 63 0.359
16
P KDN018 Kidney Disease 73 0.324
17
CNG034 Congestive Heart Failure 69 0.255
18
c CHR684 Chronic Kidney Disease 68 0.243
19
48X005 48,xyyy 37 0.229
20
P HRT032 Heart Disease 78 0.229
21
ULC004 Ulcerative Colitis 75 0.227
22
P INF037 Inflammatory Bowel Disease 57 0.224
23
HYP005 Hypokalemia 55 0.221
24
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.217
25
OST012 Osteoarthritis 80 0.216
26
MTB004 Metabolic Acidosis 48 0.215
27
LVR012 Liver Cirrhosis 67 0.214
28
ALL026 Allergic Hypersensitivity Disease 65 0.200
29
ADL002 Adult Syndrome 62 0.194
30
P NRB010 Neuroblastoma 1 66 0.192
31
P SZR006 Seizure Disorder 59 0.188
32
P DRR001 Diarrhea 55 0.186
33
CYS001 Cystic Fibrosis 84 0.186
34
c ACT071 Acute Kidney Failure 60 0.185
35
P OST002 Osteoporosis 79 0.183
36
c MGR028 Migraine with or Without Aura 1 70 0.183
37
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.180
38
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.180
39
END030 End Stage Renal Failure 60 0.180
40
HYP056 Hypoglycemia 68 0.179
41
DRM006 Dermatitis 63 0.174
42
ISC004 Ischemia 62 0.173
43
VSL002 Visual Epilepsy 58 0.172
44
HYP066 Hyperglycemia 63 0.170
45
P EPL164 Epilepsy 73 0.169
46
LSH001 Leishmaniasis 64 0.168
47
THY029 Thyroid Carcinoma 62 0.168
48
P KLZ004 Kala-Azar 1 43 0.168
49
c PNS012 Paine Syndrome 61 0.165
50
DNT012 Dental Caries 52 0.165
51
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.164
52
PNG002 Pain Agnosia 52 0.162
53
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.157
54
P CTR002 Cataract 62 0.157
55
AST005 Asthma 80 0.154
56
P HYP086 Hypothyroidism 70 0.154
57
P CLR023 Colorectal Cancer 100 0.153
58
c MCR120 Microvascular Complications of Diabetes 7 48 0.153
59
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.152
60
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.152
61
P LVR013 Liver Disease 71 0.151
62
P BRG001 Brugada Syndrome 70 0.150
63
c MCR113 Microvascular Complications of Diabetes 3 55 0.149
64
P PLM037 Pulmonary Hypertension 69 0.149
65
P GLM045 Glioma 64 0.149
66
GLL048 Glial Tumor 48 0.149
67
c MCR130 Microvascular Complications of Diabetes 6 42 0.148
68
c MCR133 Microvascular Complications of Diabetes 4 42 0.148
69
P BPL003 Bipolar Disorder 59 0.148
70
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.146
71
P PRD021 Periodic Paralysis 47 0.146
72
c MJR024 Major Affective Disorder 9 42 0.146
73
c MJR022 Major Affective Disorder 8 39 0.146
74
c THR092 Thrombophilia Due to Thrombin Defect 74 0.146
75
P DBT009 Diabetes Mellitus 66 0.146
76
P TRN020 Turner Syndrome 66 0.146
77
P MYC007 Myocardial Infarction 74 0.143
78
CNT047 Contact Dermatitis 58 0.143
79
HRW001 Hair Whorl 36 0.143
80
P CRD119 Cardiac Arrest 71 0.143
81
P LNG028 Long Qt Syndrome 68 0.142
82
P CHR345 Chronic Pain 52 0.141
83
P RHN004 Rhinitis 59 0.140
84
P ADN016 Adenocarcinoma 65 0.138
85
P HDC001 Headache 59 0.138
86
c RHB024 Rhabdomyosarcoma 2 64 0.137
87
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.137
88
HYP266 Hypoxia 58 0.137
89
P NPH012 Nephrotic Syndrome 65 0.136
90
MYT011 Myotonia 37 0.135
91
c ACT210 Acute Respiratory Distress Syndrome 59 0.134
92
DWN001 Down Syndrome 70 0.134
93
P NRC002 Narcolepsy 56 0.134
94
P VSC007 Vascular Disease 65 0.133
95
P ENC018 Encephalopathy 64 0.133
96
PLM010 Pulmonary Edema 56 0.133
97
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.131
98
THR024 Thrombosis 58 0.130
99
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.127
100
P NRP001 Neuropathy 57 0.127
101
ALL003 Allergic Rhinitis 69 0.127
102
P CNJ013 Conjunctivitis 67 0.126
103
HLX001 Helix Syndrome 46 0.126
104
CNS004 Constipation 59 0.125
105
CRB039 Cerebrovascular Disease 71 0.124
106
ATX019 Ataxia with Vitamin E Deficiency 46 0.124
107
ADN018 Adenoma 60 0.123
108
OCL069 Ocular Motor Apraxia 53 0.122
109
STR067 Stroke, Ischemic 82 0.122
110
DFC004 Deficiency Anemia 77 0.121
111
BNR002 Bone Resorption Disease 51 0.121
112
P THR014 Thrombocytopenia 67 0.121
113
PLM033 Pulmonary Embolism 60 0.121
114
CLC001 Calciphylaxis 49 0.121
115
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.120
116
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.119
117
P DBT005 Diabetes Insipidus 54 0.119
118
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.118
119
GST092 Gastroesophageal Reflux 68 0.118
120
LNG099 Lung Disease 62 0.117
121
VSC003 Visceral Leishmaniasis 55 0.116
122
STT001 Status Epilepticus 61 0.116
123
c ACT075 Acute Myocardial Infarction 59 0.116
124
P RNL015 Renal Hypertension 47 0.116
125
BRN071 Brain Injury 51 0.115
126
c ACT027 Acute Pancreatitis 60 0.114
127
P PRS040 Prostate Cancer 97 0.114
129
GLB002 Glioblastoma 74 0.113
130
GLB015 Glioblastoma Multiforme 60 0.113
131
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.113
132
c ACT068 Acute Cystitis 63 0.112
133
IRN002 Iron Metabolism Disease 58 0.112
134
P EXN002 Exanthem 58 0.111
135
ALL009 Allergic Conjunctivitis 50 0.110
136
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.109
137
HMN044 Human Immunodeficiency Virus Type 1 73 0.109
138
CHL014 Cholera 58 0.109
139
P FBR031 Febrile Seizures 54 0.109
140
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.109
141
PRM057 Paramyotonia Congenita of Von Eulenburg 45 0.109
142
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.109
143
PRT036 Peritonitis 66 0.109
144
P NTR004 Neutropenia 64 0.109
145
KRT006 Keratoconjunctivitis 53 0.109
146
PRT037 Pertussis 66 0.108
147
P CYS018 Cystitis 59 0.108
148
P TRM003 Tremor 55 0.108
149
TRM010 Traumatic Brain Injury 54 0.107
150
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.107
151
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.107
152
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.107
153
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.107
154
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.107
155
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.107
156
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.107
157
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.107
158
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.107
159
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.107
160
P LKM002 Leukemia 69 0.107
161
CTN007 Cutaneous Leishmaniasis 61 0.107
162
HYP060 Hyperinsulinism 55 0.107
163
P CRN300 Coronary Heart Disease 1 59 0.106
164
P BRS047 Breast Cancer 99 0.105
165
P ESP024 Esophagitis 62 0.105
166
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.105
167
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.105
168
P HPT023 Hepatocellular Carcinoma 99 0.105
169
c PRC016 Pre-Eclampsia 63 0.105
170
ACQ007 Acquired Immunodeficiency Syndrome 61 0.105
171
P GLM007 Glomerulonephritis 58 0.105
172
c HYP836 Hypercholesterolemia, Familial, 1 74 0.104
173
P MCR115 Microvascular Complications of Diabetes 5 67 0.103
174
P LCT001 Lactic Acidosis 52 0.103
175
HYP025 Hyperphosphatemia 47 0.103
176
CYT002 Cytokine Deficiency 46 0.103
177
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.103
178
P LNG032 Lung Cancer 99 0.103
179
P GST053 Gastric Cancer 85 0.103
180
IMM167 Immune Deficiency Disease 79 0.103
181
ATM095 Autoimmune Disease 62 0.103
182
P RHM011 Rheumatoid Arthritis 82 0.102
183
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.102
184
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.102
185
CYN003 Cyanide Poisoning 24 0.102
186
P DRM053 Dermatitis, Atopic 68 0.101
187
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.101
188
DRY001 Dry Eye Syndrome 50 0.101
189
P PSD003 Pseudohypoaldosteronism 45 0.101
190
CRB004 Cerebral Artery Occlusion 38 0.101
191
ATH013 Atherosclerosis Susceptibility 68 0.100
192
P PRD008 Periodontitis 66 0.100
193
P ATR011 Atrial Fibrillation 67 0.099
194
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.099
195
P PNC044 Pancreatitis 61 0.099
196
HYP017 Hypophosphatemia 48 0.099
197
SPN186 Spinal Cord Injury 63 0.098
198
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.098
199
URM002 Uremia 50 0.098
200
IRR003 Irritant Dermatitis 46 0.098
201
P PNM007 Pneumonia 71 0.097
202
P CRN018 Coronary Artery Anomaly 67 0.097
203
VRC005 Varicose Veins 61 0.097
204
RHM027 Rheumatic Disease 56 0.097
205
c LNG048 Long Qt Syndrome 3 50 0.097
206
EYD002 Eye Disease 59 0.096
207
ANX004 Anoxia 44 0.096
208
RCK004 Rickets 70 0.095
209
GNG013 Gingivitis 60 0.095
210
KRT001 Keratoconjunctivitis Sicca 53 0.095
211
47X002 47,xyy 49 0.095
212
c SYS001 Systemic Lupus Erythematosus 88 0.095
213
ARG004 Argyria 28 0.095
214
P CRD132 Cardiac Conduction Defect 61 0.094
215
P INT143 Interstitial Cystitis 62 0.093
216
BRN004 Brain Edema 57 0.093
217
CHL079 Children's Interstitial Lung Disease 27 0.093
218
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.092
219
P MYP004 Myopathy 63 0.092
220
TXC005 Toxic Shock Syndrome 63 0.092
221
P LPS004 Lupus Erythematosus 62 0.092
222
CHL068 Cholestasis 61 0.092
223
P GST044 Gastritis 58 0.092
224
P PRP019 Peripheral Nervous System Disease 64 0.092
225
SPS057 Spasticity 38 0.092
226
c PRS136 Prostate Cancer, Hereditary, 6 34 0.092
227
c PRS130 Prostate Cancer, Hereditary, 8 33 0.092
228
P LYM031 Lymphocytic Leukemia 56 0.091
229
P HYP076 Hyperthyroidism 55 0.091
230
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 53 0.091
231
MCL006 Macular Retinal Edema 52 0.091
232
P MLT020 Multiple Sclerosis 73 0.090
233
ANG054 Angina Pectoris 66 0.090
234
CRD223 Cardiac Arrhythmia 61 0.090
235
BCT022 Bacterial Infectious Disease 57 0.090
236
P MJR007 Major Affective Disorder 1 44 0.090
237
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.089
238
P LYM118 Lymphoma 70 0.089
239
ART140 Arteries, Anomalies of 60 0.089
240
P LDD007 Liddle Syndrome 1 58 0.089
241
P SJG008 Sjogren Syndrome 57 0.089
242
P RSP003 Respiratory Failure 75 0.088
243
P ART022 Arthritis 71 0.088
244
PRT013 Portal Hypertension 61 0.088
245
GST023 Gastric Ulcer 53 0.088
246
PPT001 Peptic Esophagitis 47 0.088
247
P BLD134 Bladder Cancer 79 0.088
248
STM007 Stomatitis 51 0.088
249
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.087
250
P RNV001 Renovascular Hypertension 49 0.087
251
MYL069 Myeloma, Multiple 85 0.086
252
ANX010 Anxiety 75 0.086
253
P PHC003 Pheochromocytoma 71 0.086
254
P ECL001 Eclampsia 53 0.086
255
ADR040 Adrenal Gland Pheochromocytoma 51 0.086
256
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.086
257
ENT004 Enthesopathy 46 0.086
258
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.086
259
c ATR087 Atrial Standstill 1 76 0.085
260
P MYL006 Myeloid Leukemia 61 0.085
261
BND020 Bone Disease 60 0.085
262
P MLG056 Malignant Hyperthermia 60 0.085
263
KRT009 Keratosis 52 0.085
264
c MLG068 Malignant Glioma 46 0.085
265
HPT004 Hepatic Coma 42 0.085
266
P ALZ034 Alzheimer Disease 90 0.084
267
GT001 Gout 63 0.084
268
P MTH007 Methemoglobinemia 47 0.084
269
RRS014 Rare Surgical Neurologic Disease 33 0.084
270
ESP021 Esophageal Cancer 90 0.084
271
P SLP006 Sleep Apnea 71 0.084
272
OST159 Osteogenic Sarcoma 67 0.084
273
DYS014 Dyspepsia 51 0.084
274
c DLT002 Dilated Cardiomyopathy 81 0.083
275
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.083
276
P URT039 Urticaria 61 0.083
277
PPT005 Peptic Ulcer Disease 60 0.083
278
ALL010 Allergic Contact Dermatitis 56 0.083
279
DBT010 Diabetic Neuropathy 56 0.083
280
GTR002 Goiter 54 0.083
281
CLC006 Calcinosis 48 0.083
282
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.083
283
P ERY008 Erythromelalgia 44 0.083
284
c MJR008 Major Affective Disorder 2 35 0.083
285
c MJR003 Major Affective Disorder 6 34 0.083
286
c MJR006 Major Affective Disorder 5 34 0.083
287
c MJR023 Major Affective Disorder 7 34 0.083
288
c MJR004 Major Affective Disorder 4 29 0.083
289
FTT001 Fatty Liver Disease 63 0.082
290
P RNL007 Renal Tubular Acidosis 49 0.082
291
PRP027 Peripheral Vascular Disease 72 0.081
292
c MCR129 Microvascular Complications of Diabetes 1 67 0.081
293
HPT019 Hepatic Encephalopathy 60 0.081
294
P PNC025 Panic Disorder 53 0.081
295
P SCK005 Sickle Cell Disease 53 0.081
296
c LKM061 Leukemia, Acute Myeloid 84 0.080
297
P SCH015 Schizophrenia 76 0.080
298
c SML038 Small Cell Cancer of the Lung 67 0.080
299
P HRP006 Herpes Simplex 66 0.080
300
P HYP069 Hyperparathyroidism 64 0.080
301
P PLY014 Polycystic Kidney Disease 61 0.080
302
GST045 Gastroenteritis 60 0.080
303
LYM019 Lymphosarcoma 48 0.080
304
KHN001 Kuhnt-Junius Degeneration 45 0.080
305
P HYP098 Hypereosinophilic Syndrome 67 0.079
306
SKN016 Skin Disease 64 0.079
307
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.079
308
NTR005 Nutritional Deficiency Disease 61 0.079
309
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.079
310
INT075 Intracranial Hypertension 54 0.079
311
P DDN001 Duodenal Ulcer 50 0.079
312
GNT046 Genetic Epilepsy with Febrile Seizures Plus 29 0.079
313
ALC007 Alcohol Dependence 68 0.078
314
P BCL017 B-Cell Lymphoma 61 0.078
315
GLS018 Glass Syndrome 51 0.078
316
KRT019 Keratitis, Hereditary 69 0.077
317
MCS002 Mucositis 56 0.077
318
MST005 Mastitis 55 0.077
319
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.076
320
P GRV001 Graves' Disease 57 0.076
321
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.076
322
BRN028 Brain Cancer 75 0.075
323
MLN008 Melanoma 68 0.075
324
P MSC005 Muscular Dystrophy 68 0.075
325
DPR016 Depression 64 0.075
326
LPD008 Lipid Metabolism Disorder 64 0.075
327
ERL001 Early Myoclonic Encephalopathy 60 0.075
328
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 58 0.075
329
SCH014 Schistosomiasis 57 0.075
330
THY030 Thyroid Gland Disease 53 0.075
331
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.075
332
P PNC035 Pancreatic Cancer 86 0.075
333
CRH001 Crohn's Disease 75 0.075
334
TTN003 Tetanus 62 0.075
335
AGN016 Aging 58 0.075
336
HPR003 Heparin-Induced Thrombocytopenia 49 0.075
337
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 68 0.074
338
P DYS154 Dystonia 65 0.074
339
c FNC043 Fanconi Anemia, Complementation Group E 64 0.074
340
PRT058 Pure Autonomic Failure 60 0.074
341
ANR040 Aneurysm 60 0.074
342
P PYL005 Pyelonephritis 58 0.074
343
SPN035 Spindle Cell Sarcoma 57 0.074
344
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.074
345
P OVR042 Ovarian Cancer 89 0.073
346
SCK003 Sickle Cell Anemia 74 0.073
347
SRC014 Sarcoma 67 0.073
348
FBR047 Fibromyalgia 60 0.073
349
INT007 Intermediate Coronary Syndrome 58 0.073
350
P AST007 Astrocytoma 52 0.073
351
HDN002 Head Injury 47 0.073
352
c PRM038 Primary Agammaglobulinemia 45 0.073
353
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.072
354
c LKM071 Leukemia, Chronic Lymphocytic 81 0.072
355
PLM001 Pulmonary Tuberculosis 72 0.072
356
P ATS364 Autism 68 0.072
357
PSY004 Psychotic Disorder 68 0.072
358
P LTR001 Lateral Sclerosis 56 0.072
359
NPH003 Nephrocalcinosis 52 0.072
360
P ACT008 Actinic Keratosis 50 0.072
361
P DNT007 Dentin Sensitivity 39 0.072
362
BRN024 Bronchitis 70 0.071
363
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.071
364
SDD001 Sudden Infant Death Syndrome 61 0.071
365
SQM006 Squamous Cell Carcinoma 60 0.071
366
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.071
367
P TMP001 Temporal Lobe Epilepsy 53 0.071
368
HYP014 Hyperuricemia 52 0.071
369
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.071
370
P HPT021 Hepatitis 69 0.070
371
P HYP370 Hypokalemic Periodic Paralysis, Type 1 62 0.070
372
NNL006 Non-Alcoholic Steatohepatitis 53 0.070
373
DBT006 Diabetic Macular Edema 46 0.070
374
c MCR112 Microvascular Complications of Diabetes 2 42 0.070
375
P FML187 Familial Hypertension 35 0.070
376
P PSR002 Psoriasis 63 0.069
377
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.069
378
SYN036 Syncope 46 0.069
379
SBC016 Subacute Delirium 43 0.069
380
ALL014 Allergic Encephalomyelitis 40 0.069
381
PPL052 Papillomatosis, Confluent and Reticulated 34 0.069
382
MDD011 Mood Disorder 62 0.067
383
P MYC008 Myocarditis 60 0.067
384
P RTN016 Retinal Degeneration 56 0.067
385
PPL022 Papilloma 56 0.067
386
LNG031 Lung Benign Neoplasm 52 0.067
387
MYL009 Myelodysplastic Syndrome 72 0.066
388
P LPR021 Leprosy 3 67 0.066
389
P HYP750 Hypertriglyceridemia, Familial 62 0.066
390
P CND004 Candidiasis 61 0.066
391
CYT008 Cytomegalovirus Infection 58 0.066
392
PST011 Pustulosis of Palm and Sole 51 0.066
393
HNS001 Hansen's Disease 35 0.066
394
P LKM062 Leukemia, Acute Lymphoblastic 68 0.065
395
P GLM040 Glioma Susceptibility 1 68 0.065
396
c HPT016 Hepatitis B 63 0.065
397
RTN017 Retinal Detachment 62 0.065
398
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.065
399
P SCK002 Sick Sinus Syndrome 56 0.065
400
HYP081 Hypolipoproteinemia 51 0.065
401
ENT011 Enterocolitis 51 0.065
402
SQM002 Squamous Cell Papilloma 49 0.065
403
P HRD086 Hereditary Hypophosphatemic Rickets 41 0.065
404
INS024 Insulin-Like Growth Factor I 79 0.064
405
IRN001 Iron Deficiency Anemia 59 0.064
406
P SLP005 Sleep Disorder 58 0.064
407
PRX015 Paroxysmal Extreme Pain Disorder 53 0.064
408
URC002 Urea Cycle Disorder 51 0.064
409
MSC007 Muscle Hypertrophy 65 0.063
410
P HMN010 Hemangioma 62 0.063
411
FCL014 Focal Epilepsy 56 0.063
412
P ART021 Arteriosclerosis 56 0.063
413
AMN003 Amnestic Disorder 55 0.063
414
THR016 Thrombophlebitis 50 0.063
415
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.063
416
CRB086 Cerebral Aneurysms 41 0.063
417
LYM133 Lymphoma, Hodgkin, Classic 70 0.062
418
MNT002 Mental Depression 60 0.062
419
ALL006 Allergic Asthma 56 0.062
420
CHR074 Choriocarcinoma 47 0.062
421
P BNG032 Benign Mesothelioma 47 0.062
422
RTN023 Retinitis 46 0.062
423
NRR001 Neuroretinitis 46 0.062
424
c LKM004 Leukemia, B-Cell, Chronic 35 0.062
425
CYT004 Cytomegalic Inclusion Disease 32 0.062
426
P CNR004 Cone-Rod Dystrophy 2 72 0.061
427
OST017 Osteomyelitis 65 0.061
428
CLN015 Colon Adenocarcinoma 65 0.061
429
P VSC011 Vasculitis 64 0.061
430
MSL001 Measles 61 0.061
431
P ADL010 Adult Respiratory Distress Syndrome 61 0.061
432
SFT003 Soft Tissue Sarcoma 57 0.061
433
SYN007 Synovitis 55 0.061
434
PLM017 Pulmonary Alveolar Microlithiasis 54 0.061
435
FDL002 Food Allergy 52 0.061
436
P FNC004 Fanconi Syndrome 48 0.061
437
PLL012 Pollen Allergy 46 0.061
438
IDP033 Idiopathic Edema 44 0.061
439
BCK006 Back Pain 44 0.061
440
ACT003 Acute Kidney Tubular Necrosis 42 0.061
441
HYP189 Hypoadrenalism 39 0.061
442
RRD056 Rare Disease in Surgical Orthopedic 29 0.061
443
SVR004 Severe Combined Immunodeficiency 74 0.060
444
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.060
445
CNN005 Connective Tissue Disease 68 0.060
446
P THL005 Thalassemia 62 0.060
447
P UVT001 Uveitis 58 0.060
448
NWB001 Newborn Respiratory Distress Syndrome 58 0.060
449
GLC003 Glucose Intolerance 55 0.060
450
ATS010 Autosomal Recessive Disease 49 0.060
451
c MLG069 Malignant Hypertension 46 0.060
452
CNT025 Central Pontine Myelinolysis 45 0.060
453
49X002 49,xxxxy Syndrome 39 0.060
454
MXD026 Mixed Glioma 36 0.060
455
NRL016 Neural Tube Defects 83 0.058
456
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.058
457
P RTN024 Retinoblastoma 74 0.058
458
APN008 Apnea, Obstructive Sleep 64 0.058
459
ACT119 Acute Promyelocytic Leukemia 63 0.058
460
c SCL052 Scleroderma, Familial Progressive 62 0.058
461
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.058
462
GST050 Gastrointestinal System Disease 57 0.058
463
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 56 0.058
464
RHM001 Rheumatic Fever 56 0.058
465
c BPL002 Bipolar I Disorder 48 0.058
466
P MYC033 Myoclonus 47 0.058
467
c FML008 Familial Retinoblastoma 46 0.058
468
TND005 Tendinitis 45 0.058
469
c HYP272 Hypercholesterolemia, Familial, 3 44 0.058
470
GST020 Gastric Antral Vascular Ectasia 42 0.058
471
PST092 Posttransplant Acute Limbic Encephalitis 29 0.058
472
ENM002 Enamel Erosion 28 0.058
473
CNN003 Conn's Syndrome 78 0.057
474
OTT002 Otitis Media 71 0.057
475
P AMY004 Amyloidosis 71 0.057
476
c BRN108 Branchiootic Syndrome 1 62 0.057
477
GTL001 Gitelman Syndrome 62 0.057
478
c HPT001 Hepatitis C 62 0.057
479
INT002 Intermittent Claudication 60 0.057
480
c FML191 Familial Long Qt Syndrome 54 0.057
481
MMM001 Mammary Paget's Disease 53 0.057
482
c INH020 Inherited Metabolic Disorder 51 0.057
483
HPT014 Hepatorenal Syndrome 49 0.057
484
GNT029 Genetic Hypertension 39 0.057
485
P SYS005 Systemic Scleroderma 68 0.056
486
c FML001 Familial Atrial Fibrillation 67 0.056
487
P NSP012 Nasopharyngeal Carcinoma 67 0.056
488
P MNN013 Meningitis 67 0.056
489
c CNG006 Congenital Hypothyroidism 65 0.056
490
P SNS001 Sensorineural Hearing Loss 62 0.056
491
P ART023 Arthropathy 61 0.056
492
IGR001 Ige Responsiveness, Atopic 61 0.056
493
BRN002 Bronchiolitis 60 0.056
494
THY122 Thyroid Gland Cancer 59 0.056
495
P SYP003 Syphilis 59 0.056
496
DSS009 Disseminated Intravascular Coagulation 58 0.056
497
ATR057 Atrioventricular Block 56 0.056
498
P HYP024 Hypoparathyroidism 56 0.056
499
LYM040 Lymphoblastic Lymphoma 54 0.056
500
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.056
501
DYS073 Dysphagia 52 0.056
502
P END047 Endophthalmitis 50 0.056
503
c MLG074 Malignant Mesenchymoma 50 0.056
504
CYT005 Cytomegalovirus Retinitis 49 0.056
505
PLP001 Pulpitis 48 0.056
506
GRN017 Granulocytopenia 46 0.056
507
IDP073 Idiopathic Hypercalciuria 43 0.056
508
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.056
509
CRV035 Cervical Cancer 77 0.055
510
P NRF023 Neurofibromatosis, Type Ii 77 0.055
511
P FLL037 Follicular Lymphoma 67 0.055
512
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.055
513
P HML002 Hemolytic Anemia 64 0.055
514
P EPL140 Epilepsy, Idiopathic Generalized 62 0.055
515
RNL024 Renal Glucosuria 59 0.055
516
P ALP008 Alopecia 58 0.055
517
P ALC033 Alcohol Use Disorder 58 0.055
518
PRS045 Prostatic Hypertrophy 55 0.055
519
IMP005 Impotence 53 0.055
520
c LRG017 Large Intestine Cancer 53 0.055
521
OST011 Osteomalacia 51 0.055
522
P OTS001 Otosclerosis 51 0.055
523
PRP080 Peripheral Artery Disease 51 0.055
524
VRN004 Vernal Keratoconjunctivitis 49 0.055
525
WTH001 Withdrawal Disorder 47 0.055
526
c CHR064 Chronic Monocytic Leukemia 43 0.055
527
P LNG064 Lung Cancer Susceptibility 3 79 0.053
528
ACR007 Acromegaly 70 0.053
529
BRK010 Burkitt Lymphoma 68 0.053
530
SKN019 Skin Melanoma 68 0.053
531
DSS008 Disease of Mental Health 66 0.053
532
IRR002 Irritable Bowel Syndrome 65 0.053
533
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.053
534
P KDN017 Kidney Cancer 60 0.053
535
c MST023 Mesothelioma, Malignant 59 0.053
536
BLR008 Bilirubin Metabolic Disorder 58 0.053
537
c GRV008 Graves Disease 1 55 0.053
538
TLN003 Telangiectasis 53 0.053
539
P RTN018 Retinal Disease 53 0.053
540
c GLL024 Gallbladder Disease 1 53 0.053
541
P MYT002 Myotonic Dystrophy 52 0.053
542
SCH012 Schizoaffective Disorder 50 0.053
543
HYP781 Hypoascorbemia 48 0.053
544
KRT002 Keratomalacia 47 0.053
545
DYS015 Dysentery 45 0.053
546
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.053
547
P CRN026 Corneal Edema 44 0.053
548
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.053
549
MLR004 Malaria 82 0.052
550
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.052
551
P PRK057 Parkinson Disease, Late-Onset 77 0.052
552
c SPN225 Spondyloarthropathy 1 74 0.052
553
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.052
554
CHL065 Cholangiocarcinoma 68 0.052
555
P NRV007 Nervous System Disease 68 0.052
556
c INF071 Inflammatory Bowel Disease 1 66 0.052
557
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 65 0.052
558
IDP011 Idiopathic Interstitial Pneumonia 65 0.052
559
P INT070 Intestinal Obstruction 60 0.052
560
c ACT073 Acute Leukemia 59 0.052
561
HMP005 Hemiplegia 55 0.052
562
INT079 Intrahepatic Cholangiocarcinoma 54 0.052
563
CRT017 Cartilage Disease 54 0.052
564
CHR073 Choreatic Disease 52 0.052
565
P THY032 Thyroiditis 52 0.052
566
PRS021 Prostatic Adenoma 52 0.052
567
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.052
568
RTC005 Reticulosarcoma 48 0.052
569
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.052
570
MCC002 Mucocutaneous Leishmaniasis 45 0.052
571
RTR008 Root Resorption 44 0.052
572
CHD004 Chudley-Mccullough Syndrome 44 0.052
573
TND004 Tendinopathy 44 0.052
574
EPC002 Epicondylitis 40 0.052
575
c SYS043 Systemic Lupus Erythematosus 1 39 0.052
576
P PRD017 Periodic Paralyses 27 0.052
577
MYT026 Myotonia Atrophica 25 0.052
578
P MDL005 Medulloblastoma 78 0.051
579
P HNT016 Huntington Disease 72 0.051
580
P MTR014 Motor Neuron Disease 66 0.051
581
P ENC004 Encephalitis 64 0.051
582
P ART005 Arteriovenous Malformation 63 0.051
583
P DRM010 Dermatomyositis 62 0.051
584
P INF032 Infertility 60 0.051
585
ERY029 Erythermalgia, Primary 58 0.051
586
PRS047 Prostatitis 57 0.051
587
P GLL022 Guillain-Barre Syndrome 56 0.051
588
PRP030 Purpura 56 0.051
589
c FML035 Familial Hyperlipidemia 56 0.051
590
P SBS003 Substance Abuse 56 0.051
591
THY124 Thyroid Gland Papillary Carcinoma 54 0.051
592
P ANG015 Angioedema 54 0.051
593
DMY004 Demyelinating Disease 54 0.051
594
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.051
595
P MYT023 Myotonia Congenita 53 0.051
596
c ACT134 Acute Liver Failure 53 0.051
597
ILS001 Ileus 51 0.051
598
LMB062 Limb Ischemia 50 0.051
599
P MGR001 Migraine Without Aura 47 0.051
600
URT010 Ureteral Obstruction 46 0.051
601
INT067 Interstitial Nephritis 46 0.051
602
PRS063 Paresthesia 46 0.051
603
c PCH010 Pachyonychia Congenita 3 43 0.051
604
P HYP120 Hypoaldosteronism 38 0.051
605
SCR003 Secretory Diarrhea 36 0.051
606
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.051
607
PRR019 Perioral Myoclonia with Absences 25 0.051
609
c LKM063 Leukemia, Chronic Myeloid 74 0.049
610
P GRF003 Graft-Versus-Host Disease 71 0.049
611
P HYP061 Hypertrophic Cardiomyopathy 68 0.049
612
P DMN002 Dementia 68 0.049
613
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.049
614
P PLM036 Pulmonary Fibrosis 66 0.049
615
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.049
616
P MVM001 Movement Disease 63 0.049
617
THY121 Thyroid Gland Anaplastic Carcinoma 62 0.049
618
HLC007 Helicobacter Pylori Infection 61 0.049
619
CHL067 Cholecystitis 60 0.049
620
c HPT003 Hepatitis a 60 0.049
621
URN010 Urinary Tract Obstruction 59 0.049
622
TNS005 Tonsillitis 58 0.049
623
TXC002 Toxic Encephalopathy 54 0.049
624
FRZ001 Frozen Shoulder 53 0.049
625
P MSC003 Muscular Atrophy 52 0.049
626
OVR082 Overgrowth Syndrome 51 0.049
627
VCC001 Vaccinia 50 0.049
628
c FLL041 Follicular Lymphoma 1 50 0.049
629
CRD137 Cardiogenic Shock 50 0.049
630
KRT008 Keratopathy 46 0.049
631
CYN002 Cyanosis, Transient Neonatal 45 0.049
632
DST006 Diastolic Heart Failure 43 0.049
633
P SBR004 Seborrheic Dermatitis 41 0.049
634
c MYC068 Myoclonic Epilepsy of Infancy 34 0.049
635
PNS018 Pain Sensitivity Quantitative Trait Locus 1 22 0.049
636
c BTT014 Beta-Thalassemia 73 0.048
637
MSC157 Muscular Dystrophy, Duchenne Type 70 0.048
638
c ATS007 Autism Spectrum Disorder 69 0.048
639
P INF038 Influenza 69 0.048
640
P OLG002 Oligodendroglioma 67 0.048
641
BRR014 Barrett Esophagus 67 0.048
642
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.048
643
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.048
644
c PRM005 Primary Hyperparathyroidism 60 0.048
645
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.048
646
HRP004 Herpes Zoster 58 0.048
647
CMM005 Common Cold 57 0.048
648
BRN056 Bronchopulmonary Dysplasia 57 0.048
649
GLS001 Gliosarcoma 56 0.048
650
P VNS003 Venous Insufficiency 55 0.048
651
PRN019 Perinatal Necrotizing Enterocolitis 55 0.048
652
MRG003 Marginal Zone B-Cell Lymphoma 55 0.048
653
HMT018 Hematopoietic Stem Cell Transplantation 54 0.048
654
PRP016 Paraplegia 54 0.048
655
PTH003 Pathologic Nystagmus 53 0.048
656
P CHL066 Cholangitis 53 0.048
657
NRT004 Neuritis 52 0.048
658
c CNT033 Central Nervous System Cancer 51 0.048
659
P RTN022 Retinal Vein Occlusion 50 0.048
660
IGG001 Iga Glomerulonephritis 50 0.048
661
SYS003 Systolic Heart Failure 43 0.048
662
BRS064 Bursitis 42 0.048
663
RDN001 Reading Disorder 42 0.048
664
MYF002 Myofascial Pain Syndrome 39 0.048
665
DNT006 Dental Pulp Necrosis 37 0.048
666
KPS004 Kaposi Sarcoma 75 0.046
667
END057 Endometrial Cancer 74 0.046
668
CRB037 Cerebral Palsy 69 0.046
669
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.046
670
P SKN015 Skin Carcinoma 67 0.046
671
P PRS038 Personality Disorder 66 0.046
672
BLL006 Bullous Pemphigoid 63 0.046
673
CTR172 Citrullinemia, Classic 62 0.046
674
WST001 West Syndrome 61 0.046
675
GRD007 Grade Iii Astrocytoma 59 0.046
676
P PRP029 Porphyria 58 0.046
677
P END033 Endocarditis 58 0.046
678
P PLY011 Polycystic Ovary Syndrome 58 0.046
679
TRD006 Tardive Dyskinesia 58 0.046
680
ERY051 Erythroleukemia, Familial 58 0.046
681
ORL005 Oral Candidiasis 56 0.046
682
P BRT004 Bartter Disease 56 0.046
683
P INT068 Intestinal Disease 56 0.046
684
END040 Endogenous Depression 55 0.046
685
P PLY019 Polyneuropathy 55 0.046
686
P NRV006 Nervous System Cancer 55 0.046
687
SPP010 Suppressor of Tumorigenicity 3 54 0.046
688
SPN051 Spondylitis 53 0.046
689
ACR041 Acromelic Frontonasal Dysostosis 50 0.046
690
c BRG005 Brugada Syndrome 1 50 0.046
691
P OPN001 Open-Angle Glaucoma 50 0.046
692
PRS129 Prostatic Hyperplasia, Benign 49 0.046
693
P TCL004 T-Cell Leukemia 48 0.046
694
SNT005 Sinoatrial Node Disease 46 0.046
695
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.046
696
ENT001 Enterocele 44 0.046
697
P HYP265 Hypotonia 43 0.046
698
ATM052 Autoimmune Disease 1 38 0.046
699
RTC003 Root Caries 37 0.046
700
SCR011 Scrapie 37 0.046
701
c LKM005 Leukemia, T-Cell, Chronic 35 0.046
702
INF009 Inflammatory Spondylopathy 29 0.046
703
MTH071 Methane Production 26 0.046
704
c MNN043 Meningioma, Familial 74 0.045
705
MNT001 Mantle Cell Lymphoma 69 0.045
706
P MJR001 Major Depressive Disorder 69 0.045
707
MNN042 Meningioma, Radiation-Induced 64 0.045
708
VRL011 Viral Infectious Disease 62 0.045
709
ARG002 Argininosuccinic Aciduria 59 0.045
710
c THY102 Thyroid Cancer, Nonmedullary, 2 59 0.045
711
P OPT006 Optic Nerve Disease 59 0.045
712
TRG002 Trigeminal Neuralgia 58 0.045
713
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.045
714
P EPD016 Epidermolysis Bullosa 54 0.045
715
DFF036 Differentiated Thyroid Carcinoma 53 0.045
716
NRT001 Neurotic Disorder 53 0.045
717
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.045
718
SCH003 Schizophreniform Disorder 49 0.045
719
P OBS001 Obstructive Jaundice 49 0.045
720
PLS025 Plasmablastic Lymphoma 48 0.045
721
KRT013 Keratolytic Winter Erythema 45 0.045
722
MYC005 Myocardial Stunning 45 0.045
723
INP001 Inappropriate Adh Syndrome 45 0.045
724
P CLS010 Cluster Headache 44 0.045
725
SPN021 Spinal Meningioma 40 0.045
726
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.045
727
SCR001 Secretory Meningioma 38 0.045
728
LYM048 Lymphoma, Large-Cell, Immunoblastic 30 0.045
729
LPT014 Leptin Deficiency or Dysfunction 72 0.043
730
P MYC084 Mycobacterium Tuberculosis 1 69 0.043
731
c JVN010 Juvenile Rheumatoid Arthritis 67 0.043
732
MYL031 Myeloproliferative Neoplasm 66 0.043
733
P MST009 Mastocytosis 62 0.043
734
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.043
735
CHR066 Chronic Fatigue Syndrome 61 0.043
736
ING001 Inguinal Hernia 61 0.043
737
P CHR285 Chronic Myelomonocytic Leukemia 60 0.043
738
CHL123 Chlamydia 60 0.043
739
P BRN022 Bronchiectasis 60 0.043
740
HMR039 Hemorrhage, Intracerebral 59 0.043
741
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 58 0.043
742
TRN018 Transitional Cell Carcinoma 57 0.043
743
c PRD040 Periodontitis, Chronic 56 0.043
744
HRT012 Heart Valve Disease 56 0.043
745
c SCN007 Secondary Hyperparathyroidism 52 0.043
746
NTR046 Neutrophil Migration 49 0.043
747
RNL077 Renal Fibrosis 49 0.043
748
c HPT015 Hepatitis D 49 0.043
749
SPL004 Splenic Marginal Zone Lymphoma 48 0.043
750
ASP007 Aspiration Pneumonia 46 0.043
751
PPL001 Papillary Adenoma 42 0.043
752
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.043
753
MYX004 Myxedema 41 0.043
754
c HMG029 Hemoglobin Se Disease 40 0.043
755
c ACT004 Acute Diarrhea 38 0.043
756
c CHR098 Chronic Pyelonephritis 38 0.043
757
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 37 0.043
758
GRM010 Germ Cells Tumors 35 0.043
759
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.043
760
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 28 0.043
761
LTH043 Lithium Transport 18 0.043
762
ART016 Aortic Aneurysm 71 0.041
763
BRT054 Brittle Bone Disorder 71 0.041
764
GST040 Gastric Adenocarcinoma 67 0.041
765
P BLD062 Bile Duct Cancer 66 0.041
766
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.041
767
CLR108 Colorectal Adenoma 64 0.041
768
HMT002 Hematologic Cancer 64 0.041
769
PPL049 Papillon-Lefevre Syndrome 63 0.041
770
P RHB003 Rhabdomyosarcoma 62 0.041
771
TRN015 Transient Cerebral Ischemia 62 0.041
772
INT066 Interstitial Lung Disease 61 0.041
773
DPH001 Diphtheria 61 0.041
774
INS001 Insulinoma 60 0.041
775
c ADL017 Adult T-Cell Leukemia 59 0.041
776
P MYP006 Myopia 58 0.041
777
PLM031 Poliomyelitis 58 0.041
778
HPT022 Hepatoblastoma 58 0.041
779
PLS011 Plasmacytoma 57 0.041
780
P BNC003 Bone Cancer 56 0.041
781
PNM008 Pneumothorax 56 0.041
782
MTH009 Mouth Disease 56 0.041
783
c PSR017 Psoriasis 2 55 0.041
784
ACT058 Active Peptic Ulcer Disease 55 0.041
785
SPT004 Septic Arthritis 55 0.041
786
P RCT021 Rectum Cancer 54 0.041
787
OCL006 Ocular Hypertension 52 0.041
788
BNN003 Bone Inflammation Disease 51 0.041
789
P SHR001 Short Bowel Syndrome 50 0.041
790
ESP002 Esophageal Varix 49 0.041
791
ATN005 Autonomic Dysfunction 48 0.041
792
BNM001 Bone Marrow Cancer 48 0.041
793
ANR004 Anuria 47 0.041
794
HMP009 Haemophilus Influenzae 46 0.041
795
P DST107 Distal Renal Tubular Acidosis 45 0.041
796
ASP008 Aspiration Pneumonitis 41 0.041
797
SPR126 Superior Semicircular Canal Dehiscence 39 0.041
798
OVR094 Ovarian Epithelial Cancer 39 0.041
800
c CHR682 Chronic Bilirubin Encephalopathy 36 0.041
801
PLY150 Polykaryocytosis Inducer 31 0.041
802
RSP007 Respiratory Distress Syndrome, Infant 31 0.041
804
c FML159 Familial Periodic Paralyses 17 0.041
805
P SRC025 Sarcoidosis 1 72 0.040
806
CRP001 Carpal Tunnel Syndrome 68 0.040
807
c FML021 Familial Hypercholesterolemia 67 0.040
808
ANR007 Anorexia Nervosa 64 0.040
809
HSH003 Hashimoto Thyroiditis 63 0.040
810
P END044 Endometriosis 63 0.040
811
OST003 Osteonecrosis 62 0.040
812
NRM005 Neuromuscular Disease 62 0.040
813
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 60 0.040
814
c MCL013 Mucolipidosis Iv 60 0.040
815
P BRS044 Breast Adenocarcinoma 59 0.040
816
P PGT001 Paget's Disease of Bone 59 0.040
817
LYM027 Lymphopenia 58 0.040
818
YLL002 Yellow Fever 58 0.040
819
ERY003 Erythema Multiforme 57 0.040
820
c VRL010 Viral Hepatitis 56 0.040
821
P PMP001 Pemphigus 56 0.040
822
MNR012 Meniere Disease 56 0.040
823
P INS002 in Situ Carcinoma 55 0.040
824
RSC001 Rosacea 55 0.040
825
P LYM025 Lymphedema 54 0.040
826
P MYS005 Myositis 54 0.040
827
P HYP083 Hypopituitarism 53 0.040
828
BRN038 Bronchial Disease 53 0.040
829
THY123 Thyroid Gland Follicular Carcinoma 52 0.040
830
CLR109 Colorectal Adenocarcinoma 51 0.040
831
CHL004 Cholelithiasis 50 0.040
832
NRM004 Neuroma 50 0.040
833
c PSR023 Psoriasis 1 50 0.040
834
MYL075 Myelodysplastic/myeloproliferative Neoplasm 50 0.040
835
RYN005 Raynaud Phenomenon 50 0.040
836
MCR004 Macroglobulinemia 50 0.040
837
c INF145 Infantile Liver Failure Syndrome 1 50 0.040
838
c BCT013 Bacterial Pneumonia 49 0.040
839
NRL004 Neuroleptic Malignant Syndrome 48 0.040
840
VTM033 Vitamin K Deficiency Bleeding 47 0.040
841
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 46 0.040
842
CCC002 Coccidiosis 46 0.040
843
P BCT020 Bacteremia 2 45 0.040
844
ORL015 Oral Squamous Cell Carcinoma 44 0.040
845
DRG024 Drug Allergy 43 0.040
846
ATN004 Autonomic Neuropathy 43 0.040
847
APP009 Appendix Adenocarcinoma 43 0.040
848
GNG003 Gingival Recession 43 0.040
849
TRP009 Triple X Syndrome 42 0.040
850
SNL007 Senile Cataract 41 0.040
851
c PSR028 Psoriasis 7 40 0.040
852
c PSR018 Psoriasis 13 40 0.040
853
c PSR032 Psoriasis 11 40 0.040
854
HYP264 Hypertonia 39 0.040
855
FRN014 Fournier Gangrene 38 0.040
856
PRR001 Periarthritis 30 0.040
857
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.040
858
P SCN067 Scn1a Seizure Disorders 21 0.040
859
P ATX030 Ataxia-Telangiectasia 83 0.038
860
c HPT073 Hepatitis C Virus 74 0.038
861
ADR007 Adrenoleukodystrophy 72 0.038
862
EWN003 Ewing Sarcoma 69 0.038
863
CYS013 Cystinuria 66 0.038
864
P OCL013 Oculodentodigital Dysplasia 65 0.038
865
FCT007 Factor Vii Deficiency 65 0.038
866
c ALP101 Alpha-Thalassemia 63 0.038
867
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.038
868
P ALP009 Alopecia Areata 61 0.038
869
c DNG003 Dengue Disease 61 0.038
870
P EPN002 Ependymoma 61 0.038
871
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.038
872
P PTN014 Patent Ductus Arteriosus 1 60 0.038
873
c CNT035 Central Nervous System Disease 56 0.038
874
PRT038 Protein-Energy Malnutrition 56 0.038
875
P MTR003 Mitral Valve Stenosis 54 0.038
876
c PRM092 Primary Lateral Sclerosis, Adult, 1 54 0.038
877
GNT002 Giant Cell Glioblastoma 52 0.038
878
THR004 Thrombocytosis 52 0.038
879
P THR015 Thrombophilia 51 0.038
881
BRD004 Borderline Personality Disorder 51 0.038
882
APL002 Aplasia of Lacrimal and Salivary Glands 51 0.038
883
IMM064 Immunodeficiency, Common Variable, 10 51 0.038
884
PRT018 Portal Vein Thrombosis 50 0.038
885
ATY042 Atypical Chronic Myeloid Leukemia 50 0.038
886
RFR010 Refractory Anemia 50 0.038
887
P HMN032 Human Herpesvirus 8 49 0.038
888
BCT004 Bacteriuria 48 0.038
889
c BNG030 Benign Ependymoma 48 0.038
890
c PRM093 Premature Ovarian Failure 7 48 0.038
891
c DRM054 Dermatitis, Atopic, 2 45 0.038
892
DNT001 Dental Fluorosis 44 0.038
893
DMP001 Dumping Syndrome 44 0.038
894
CRT015 Carotid Artery Occlusion 44 0.038
895
P MYG005 Myoglobinuria 43 0.038
896
c FML036 Familial Periodic Paralysis 42 0.038
897
c TCL024 T-Cell Non-Hodgkin Lymphoma 37 0.038
898
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 36 0.038
899
EXN003 Exencephaly 32 0.038
900
OCC001 Occupational Dermatitis 30 0.038
901
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.038
902
CYT018 Cytochrome P450 2d6 Variant 28 0.038
903
NND001 Nondystrophic Myotonia 20 0.038
904
P APL001 Aplastic Anemia 76 0.036
905
ACR006 Aceruloplasminemia 74 0.036
906
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.036
907
P HYD006 Hydrocephalus 68 0.036
908
P ORT004 Orthostatic Intolerance 68 0.036
909
c ART101 Aortic Valve Disease 2 67 0.036
910
MYC006 Mycosis Fungoides 67 0.036
911
BRC012 Brucellosis 62 0.036
912
ORL011 Oral Cancer 62 0.036
913
APP008 Appendicitis 61 0.036
914
P TXP001 Toxoplasmosis 61 0.036
915
c DWL002 Dowling-Degos Disease 1 59 0.036
916
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.036
917
c ESS001 Essential Tremor 58 0.036
918
P STR020 Strabismus 57 0.036
919
APH002 Aphasia 56 0.036
920
CLL003 Cellulitis 56 0.036
921
CMR002 Coumarin Resistance 56 0.036
922
PHR003 Pharyngitis 56 0.036
923
c CNG216 Congenital Hydrocephalus 55 0.036
924
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.036
925
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.036
926
HMC014 Homocysteinemia 54 0.036
927
MCN017 Meconium Ileus 54 0.036
928
P SLM003 Salmonellosis 54 0.036
929
CHR100 Chronic Ulcer of Skin 53 0.036
930
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.036
931
HRT011 Heart Septal Defect 52 0.036
932
P BRN035 Brain Stem Glioma 51 0.036
933
P THY054 Thyrotoxic Periodic Paralysis 51 0.036
934
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 0.036
935
SPL018 Splenomegaly 48 0.036
936
STT002 Status Asthmaticus 47 0.036
937
PRP007 Priapism 47 0.036
938
LWC001 Low Compliance Bladder 45 0.036
939
P HMP006 Hemiplegic Migraine 45 0.036
940
NWC001 Newcastle Disease 45 0.036
941
DBT002 Diabetic Autonomic Neuropathy 45 0.036
942
ANP009 Anaplastic Oligodendroglioma 44 0.036
943
PLR007 Pleural Empyema 44 0.036
944
c MLG079 Malignant Pleural Mesothelioma 43 0.036
945
c FML297 Familial Thyroid Dyshormonogenesis 43 0.036
946
GLC086 Glucocorticoid-Induced Osteoporosis 42 0.036
947
P HYP263 Hypersomnia 42 0.036
948
P GLM044 Glomerular Disease 42 0.036
949
AMN002 Amino Acid Metabolic Disorder 42 0.036
950
NSP002 Nasopharyngitis 41 0.036
951
HPT082 Hepatic Adenomas, Familial 40 0.036
952
MST004 Mast Cell Neoplasm 40 0.036
953
ART008 Arteriosclerosis Obliterans 40 0.036
954
ALD013 Aldosterone-Producing Adenoma 39 0.036
955
EXT007 Extracutaneous Mastocytoma 39 0.036
956
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.036
957
c HYP606 Hypokalemic Periodic Paralysis, Type 2 35 0.036
958
MCH006 Mechanical Strabismus 31 0.036
959
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.036
960
P ATR081 Atrial Standstill 29 0.036
961
MNG007 Manganese Poisoning 28 0.036
962
EXF003 Exfoliative Dermatitis 28 0.036
963
NRM009 Normokalemic Periodic Paralysis 28 0.036
964
HML018 Homologous Wasting Disease 22 0.036
965
AMN012 Aminoacidopathies 22 0.036
966
P INB001 Inborn Amino Acid Metabolism Disorder 11 0.036
967
P FML011 Familial Adenomatous Polyposis 73 0.034
968
c EXD008 Exudative Vitreoretinopathy 1 69 0.034
969
ACR008 Acrocallosal Syndrome 66 0.034
970
CHG001 Chagas Disease 66 0.034
971
INC002 Inclusion Body Myositis 66 0.034
972
P SPN046 Spinal Muscular Atrophy 65 0.034
973
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.034
974
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.034
975
ETN001 Eating Disorder 61 0.034
976
P ERL057 Early Infantile Epileptic Encephalopathy 60 0.034
977
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.034
978
P HRD011 Hereditary Spherocytosis 59 0.034
979
HYD002 Hydronephrosis 58 0.034
980
P MTC069 Mitochondrial Disorders 57 0.034
981
c LNG047 Long Qt Syndrome 2 57 0.034
982
PRM236 Primary Biliary Cholangitis 57 0.034
983
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 57 0.034
984
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.034
985
P FBR017 Fibrosarcoma 57 0.034
986
GLL018 Gallbladder Cancer 57 0.034
987
HMG005 Hemoglobinopathy 57 0.034
988
INT030 Intracranial Aneurysm 57 0.034
989
APH001 Aphthous Stomatitis 56 0.034
990
APP015 Apparent Mineralocorticoid Excess 56 0.034
991
P PLY018 Polycythemia 56 0.034
992
c CHR417 Chronic Graft Versus Host Disease 56 0.034
993
LST001 Listeriosis 55 0.034
994
CHL028 Childhood Type Dermatomyositis 55 0.034
995
DCB001 Decubitus Ulcer 54 0.034
996
PRC013 Pericarditis 54 0.034
997
c FML023 Familial Hemiplegic Migraine 54 0.034
998
CHC001 Chickenpox 53 0.034
999
P PTT006 Pituitary Adenoma 53 0.034
1000
P MGR003 Migraine with Aura 53 0.034
1001
CND002 Conduct Disorder 52 0.034
1002
P CNT005 Central Nervous System Lymphoma 52 0.034
1003
P RNL017 Renal Oncocytoma 52 0.034
1004
PYD002 Pyoderma 51 0.034
1005
c XNT010 Xanthinuria, Type I 51 0.034
1006
PLR008 Pleurisy 50 0.034
1007
c NRC009 Narcolepsy 1 50 0.034
1008
CRN030 Coronary Stenosis 49 0.034
1009
P END046 Endometritis 49 0.034
1010
MTN003 Motion Sickness 48 0.034
1011
PLY012 Polyhydramnios 48 0.034
1012
PRM020 Premenstrual Tension 48 0.034
1013
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.034
1014
c PRG043 Progressive Familial Heart Block, Type Ib 48 0.034
1015
c ANT034 Anterior Uveitis 48 0.034
1016
BHR001 Behr Syndrome 47 0.034
1017
P HMR005 Hemorrhoid 47 0.034
1018
BRN014 Bronchopneumonia 47 0.034
1019
MGC001 Megacolon 47 0.034
1020
PTT037 Pituitary Tumors 47 0.034
1021
FSC004 Fasciitis 47 0.034
1022
GLC022 Glucose/galactose Malabsorption 46 0.034
1023
ART031 Aortic Coarctation 45 0.034
1024
P HYP733 Hypercalciuria, Absorptive, 2 45 0.034
1025
DVR002 Diverticulitis 44 0.034
1026
PRC003 Proctitis 44 0.034
1027
PRP017 Periapical Periodontitis 43 0.034
1028
DFF003 Diffuse Scleroderma 43 0.034
1029
RMS001 Rem Sleep Behavior Disorder 43 0.034
1030
P MLT008 Multinodular Goiter 42 0.034
1031
HYP540 Hypertension, Diastolic 41 0.034
1032
C1N001 C1 Inhibitor Deficiency 39 0.034
1033
MYL074 Myelodysplastic Syndrome with Excess Blasts 37 0.034
1034
CHR178 Chromosomal Triplication 36 0.034
1035
ACT011 Acute Contagious Conjunctivitis 35 0.034
1037
P VSC018 Visceral Steatosis 34 0.034
1038
PHT008 Photosensitive Epilepsy 34 0.034
1039
P RNL115 Renal Tubular Acidosis, Proximal 31 0.034
1040
P CNT036 Central Nervous System Germ Cell Tumor 28 0.034
1041
ADG002 Audiogenic Seizures 25 0.034
1042
OSM001 Osmotic Diarrhea 25 0.034
1043
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.032
1044
c WLM013 Wilms Tumor 1 69 0.032
1045
PNC129 Pancreatic Adenocarcinoma 69 0.032
1046
OBS002 Obsessive-Compulsive Disorder 69 0.032
1047
P ASP006 Aspergillosis 67 0.032
1048
c LNG044 Long Qt Syndrome 1 66 0.032
1049
CRN036 Craniopharyngioma 65 0.032
1050
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.032
1051
c WLM018 Wilms Tumor 5 63 0.032
1052
CHY002 Chylomicron Retention Disease 63 0.032
1053
LYM012 Lymphoplasmacytic Lymphoma 62 0.032
1054
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.032
1055
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.032
1056
P MCH002 Machado-Joseph Disease 61 0.032
1057
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.032
1058
SPP011 Suppression of Tumorigenicity 12 61 0.032
1059
PST028 Post-Traumatic Stress Disorder 60 0.032
1060
SZR001 Sezary's Disease 59 0.032
1061
P PRV006 Pervasive Developmental Disorder 58 0.032
1062
CHR177 Chromophobe Renal Cell Carcinoma 58 0.032
1063
GST033 Gestational Diabetes 58 0.032
1064
LMY014 Leiomyoma, Uterine 57 0.032
1065
P MLN007 Male Infertility 57 0.032
1066
HRY003 Hairy Cell Leukemia 57 0.032
1067
P PLC011 Pilocytic Astrocytoma 57 0.032
1068
RSP006 Respiratory System Disease 57 0.032
1069
PMP006 Pemphigus Vulgaris, Familial 56 0.032
1070
CRH005 Crohn's Colitis 56 0.032
1071
MYP139 Myopathy, Proximal, and Ophthalmoplegia 56 0.032
1072
SNS003 Sensory Peripheral Neuropathy 56 0.032
1073
BRN012 Bronchiolitis Obliterans 55 0.032
1074
P OPT009 Optic Neuritis 55 0.032
1075
P PRM006 Primary Biliary Cirrhosis 54 0.032
1076
VGN023 Vaginitis 54 0.032
1077
HMS001 Hemosiderosis 54 0.032
1078
P PTS002 Ptosis 53 0.032
1079
ALC009 Alcoholic Liver Cirrhosis 53 0.032
1080
SPS003 Spastic Diplegia 53 0.032
1081
LMY002 Leiomyoma 52 0.032
1082