Search results for Magnesium

1350 hits were found for Magnesium

# Family MCID Name MIFTS Score
1
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 45 9.073
2
c HYP210 Hypomagnesemia 2, Renal 43 6.835
3
HYP550 Hypomagnesemia 1, Intestinal 45 4.037
4
GTL001 Gitelman Syndrome 65 4.017
5
P HYP534 Hypomagnesemia 3, Renal 48 3.323
6
MGN003 Magnesium, Elevated Red Cell 6 2.314
7
DSR028 Disorder of Magnesium Transport 3 2.298
8
c PRC016 Pre-Eclampsia 63 0.487
9
P ECL001 Eclampsia 50 0.457
10
PNG002 Pain Agnosia 51 0.310
11
c ACT075 Acute Myocardial Infarction 57 0.275
12
CRB037 Cerebral Palsy 69 0.268
13
HYP005 Hypokalemia 55 0.258
14
c SVR005 Severe Pre-Eclampsia 50 0.257
15
P KDN018 Kidney Disease 72 0.254
16
c HYP595 Hypertension, Essential 84 0.245
17
P MYC007 Myocardial Infarction 70 0.232
18
CNG034 Congestive Heart Failure 69 0.223
19
P SZR006 Seizure Disorder 56 0.221
20
AST005 Asthma 76 0.213
21
c MGR028 Migraine with or Without Aura 1 67 0.207
22
VSL002 Visual Epilepsy 59 0.201
23
c CHR684 Chronic Kidney Disease 70 0.195
24
P DBT009 Diabetes Mellitus 64 0.194
25
URL001 Urolithiasis 45 0.193
26
48X005 48,xyyy 39 0.188
27
BNR002 Bone Resorption Disease 48 0.187
28
P HRT032 Heart Disease 75 0.182
29
ALC007 Alcohol Dependence 66 0.179
30
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.177
31
c PNS012 Paine Syndrome 61 0.177
32
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.177
33
P HYP069 Hyperparathyroidism 63 0.175
34
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.172
35
P CRN300 Coronary Heart Disease 1 63 0.171
36
P DRR001 Diarrhea 55 0.171
37
BRN071 Brain Injury 49 0.169
38
ISC004 Ischemia 58 0.168
39
CNS004 Constipation 58 0.167
40
TRM010 Traumatic Brain Injury 51 0.167
41
P ATR011 Atrial Fibrillation 66 0.165
42
P PRC031 Preeclampsia/eclampsia 1 38 0.162
43
P CRD119 Cardiac Arrest 67 0.159
44
LPP008 Lipoprotein Quantitative Trait Locus 62 0.157
45
RCK004 Rickets 68 0.154
46
ART140 Arteries, Anomalies of 52 0.153
47
P LVR013 Liver Disease 68 0.152
48
P OST002 Osteoporosis 74 0.151
49
TTN003 Tetanus 65 0.149
50
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.148
51
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.148
52
ATH013 Atherosclerosis Susceptibility 65 0.148
53
P VSC007 Vascular Disease 63 0.148
54
P ENC018 Encephalopathy 61 0.147
55
NPH009 Nephrolithiasis 55 0.147
56
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.147
57
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.147
58
P HDC001 Headache 57 0.145
59
P PLM037 Pulmonary Hypertension 67 0.143
60
P HYP024 Hypoparathyroidism 56 0.143
61
P CLR023 Colorectal Cancer 99 0.141
62
LVR012 Liver Cirrhosis 62 0.140
63
NPH003 Nephrocalcinosis 51 0.140
64
DPR016 Depression 63 0.138
65
END086 End Stage Renal Disease 51 0.136
66
STR067 Stroke, Ischemic 81 0.134
67
HYP266 Hypoxia 57 0.133
68
GST092 Gastroesophageal Reflux 67 0.131
69
CRB039 Cerebrovascular Disease 67 0.131
70
P BND020 Bone Disease 59 0.131
71
SBC016 Subacute Delirium 44 0.131
72
P NRP001 Neuropathy 56 0.130
73
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.128
74
LPD008 Lipid Metabolism Disorder 62 0.128
75
CRD223 Cardiac Arrhythmia 60 0.127
76
HYP066 Hyperglycemia 61 0.123
77
HYP025 Hyperphosphatemia 48 0.122
78
ANX010 Anxiety 73 0.120
79
OCL069 Ocular Motor Apraxia 51 0.120
80
CRD132 Cardiac Conduction Defect 58 0.117
81
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.114
82
ADL002 Adult Syndrome 70 0.114
83
P HYP086 Hypothyroidism 69 0.114
84
IRN002 Iron Metabolism Disease 57 0.114
85
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.114
86
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.114
87
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.114
88
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.114
89
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.114
90
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.114
91
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.114
92
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.114
93
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.114
94
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.114
95
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.112
96
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.112
97
P CHR345 Chronic Pain 44 0.112
98
DFC004 Deficiency Anemia 70 0.110
99
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.110
100
SPN186 Spinal Cord Injury 60 0.110
101
LNG099 Lung Disease 60 0.110
102
MNT002 Mental Depression 58 0.110
103
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.110
104
P RSP003 Respiratory Failure 74 0.108
105
c RHB024 Rhabdomyosarcoma 2 67 0.108
106
c ACT071 Acute Kidney Failure 60 0.108
107
PRM020 Premenstrual Tension 40 0.108
108
P PHC003 Pheochromocytoma 71 0.106
109
ALL026 Allergic Hypersensitivity Disease 62 0.106
110
ADR040 Adrenal Gland Pheochromocytoma 46 0.106
111
ADG002 Audiogenic Seizures 25 0.105
112
P BRS047 Breast Cancer 97 0.103
113
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.103
114
NTR005 Nutritional Deficiency Disease 62 0.103
115
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.103
116
P ART021 Arteriosclerosis 54 0.103
117
STT002 Status Asthmaticus 50 0.103
118
HDN002 Head Injury 46 0.103
119
P TRN020 Turner Syndrome 67 0.101
120
ANG054 Angina Pectoris 66 0.101
121
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.101
122
TXC005 Toxic Shock Syndrome 62 0.101
123
GST033 Gestational Diabetes 61 0.101
124
c PRM005 Primary Hyperparathyroidism 58 0.101
125
P HYP076 Hyperthyroidism 55 0.101
126
PLC007 Placental Abruption 48 0.101
127
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.101
128
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.099
129
OST012 Osteoarthritis 78 0.099
130
P CNR004 Cone-Rod Dystrophy 2 73 0.099
131
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.099
132
FBR047 Fibromyalgia 58 0.099
133
P SCK005 Sickle Cell Disease 50 0.099
134
FTT001 Fatty Liver Disease 61 0.097
135
P PNC044 Pancreatitis 61 0.097
136
P LTR001 Lateral Sclerosis 54 0.097
137
HLX001 Helix Syndrome 47 0.097
138
HRW001 Hair Whorl 36 0.097
139
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.095
140
c ACT027 Acute Pancreatitis 60 0.095
141
THR024 Thrombosis 57 0.095
142
HYP017 Hypophosphatemia 50 0.095
143
c ATR087 Atrial Standstill 1 75 0.093
144
DWN001 Down Syndrome 70 0.093
145
c DBT099 Diabetes Mellitus, Type I 65 0.093
146
CHR066 Chronic Fatigue Syndrome 61 0.093
147
SDD001 Sudden Infant Death Syndrome 61 0.093
148
P PRP019 Peripheral Nervous System Disease 58 0.093
149
P CRD246 Cardiovascular System Disease 57 0.093
150
PRV004 Periventricular Leukomalacia 52 0.093
151
c SCN007 Secondary Hyperparathyroidism 51 0.093
152
MTB004 Metabolic Acidosis 50 0.093
153
c HYP836 Hypercholesterolemia, Familial, 1 73 0.091
154
P EPL164 Epilepsy 71 0.091
155
PPL049 Papillon-Lefevre Syndrome 65 0.091
156
P ORT004 Orthostatic Intolerance 62 0.091
157
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.091
158
ADN018 Adenoma 59 0.091
159
BRN004 Brain Edema 56 0.091
160
ATX019 Ataxia with Vitamin E Deficiency 42 0.091
161
CHL079 Children's Interstitial Lung Disease 26 0.091
162
SCK003 Sickle Cell Anemia 74 0.088
163
P ESP024 Esophagitis 62 0.088
164
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.088
165
47X002 47,xyy 49 0.088
166
PRM237 Primary Hypomagnesemia 43 0.088
167
HRN029 Hearing Loss, Noise-Induced 37 0.088
168
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.086
169
P TRM003 Tremor 54 0.086
170
SPS003 Spastic Diplegia 51 0.086
171
ANX004 Anoxia 40 0.086
172
OST159 Osteogenic Sarcoma 66 0.084
173
c FML001 Familial Atrial Fibrillation 65 0.084
174
P HYP750 Hypertriglyceridemia, Familial 62 0.084
175
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.084
176
PPT005 Peptic Ulcer Disease 59 0.084
177
P ALC033 Alcohol Use Disorder 58 0.084
178
P DDN001 Duodenal Ulcer 52 0.084
179
CHR005 Chorioamnionitis 51 0.084
180
CLC006 Calcinosis 48 0.084
181
c DRR009 Diarrhea 6 46 0.084
182
IMM167 Immune Deficiency Disease 78 0.082
183
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.082
184
P MCR115 Microvascular Complications of Diabetes 5 66 0.082
185
P THL005 Thalassemia 60 0.082
186
P PLY011 Polycystic Ovary Syndrome 56 0.082
187
AGN016 Aging 56 0.082
188
PLM010 Pulmonary Edema 54 0.082
189
WTH001 Withdrawal Disorder 48 0.082
190
P ATS364 Autism 70 0.079
191
P ART023 Arthropathy 62 0.079
192
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.079
193
P GLM007 Glomerulonephritis 57 0.079
194
P INF037 Inflammatory Bowel Disease 54 0.079
195
c MCR113 Microvascular Complications of Diabetes 3 52 0.079
196
ILS001 Ileus 51 0.079
197
c MCR120 Microvascular Complications of Diabetes 7 47 0.079
198
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.079
199
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.079
200
P HYP265 Hypotonia 43 0.079
201
c MCR130 Microvascular Complications of Diabetes 6 41 0.079
202
c MCR133 Microvascular Complications of Diabetes 4 41 0.079
203
P PSD087 Pseudoxanthoma Elasticum 65 0.077
204
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.077
205
P CTR002 Cataract 60 0.077
206
P ANP001 Anaplastic Large Cell Lymphoma 58 0.077
207
ATR057 Atrioventricular Block 55 0.077
208
INT007 Intermediate Coronary Syndrome 55 0.077
209
HYP060 Hyperinsulinism 54 0.077
210
GLC003 Glucose Intolerance 54 0.077
211
P ALZ034 Alzheimer Disease 88 0.074
212
P SCH015 Schizophrenia 74 0.074
213
P LNG028 Long Qt Syndrome 66 0.074
214
c FNC043 Fanconi Anemia, Complementation Group E 62 0.074
215
MDD011 Mood Disorder 62 0.074
216
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.074
217
OST011 Osteomalacia 52 0.074
218
URM002 Uremia 49 0.074
219
HPT004 Hepatic Coma 45 0.074
220
CRB004 Cerebral Artery Occlusion 45 0.074
221
P GST053 Gastric Cancer 83 0.071
222
c DLT002 Dilated Cardiomyopathy 79 0.071
223
HMN044 Human Immunodeficiency Virus Type 1 71 0.071
224
STT001 Status Epilepticus 60 0.071
225
BRN002 Bronchiolitis 59 0.071
226
NNL006 Non-Alcoholic Steatohepatitis 54 0.071
227
DNT012 Dental Caries 53 0.071
228
P RCT021 Rectum Cancer 52 0.071
229
ASP004 Asphyxia Neonatorum 46 0.071
230
P BRB001 Beriberi 46 0.071
231
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.071
232
CYT002 Cytokine Deficiency 42 0.071
233
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.071
234
P OVR042 Ovarian Cancer 88 0.068
235
c BTT014 Beta-Thalassemia 74 0.068
236
P MYP004 Myopathy 70 0.068
237
P LKM002 Leukemia 68 0.068
238
P MJR001 Major Depressive Disorder 68 0.068
239
P MLG056 Malignant Hyperthermia 67 0.068
240
P DMN002 Dementia 66 0.068
241
CHL068 Cholestasis 61 0.068
242
DRM006 Dermatitis 61 0.068
243
P SLP005 Sleep Disorder 59 0.068
244
BRD001 Brody Myopathy 57 0.068
245
GST050 Gastrointestinal System Disease 56 0.068
246
PRT082 Preterm Premature Rupture of the Membranes 54 0.068
247
P SHR001 Short Bowel Syndrome 53 0.068
248
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.068
249
GST023 Gastric Ulcer 53 0.068
250
ENT011 Enterocolitis 51 0.068
251
HYP781 Hypoascorbemia 51 0.068
252
RNL011 Renal Osteodystrophy 50 0.068
253
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.068
254
CRN019 Coronary Artery Vasospasm 46 0.068
255
P HYP098 Hypereosinophilic Syndrome 67 0.066
256
c MCR129 Microvascular Complications of Diabetes 1 66 0.066
257
P ADN016 Adenocarcinoma 64 0.066
258
SKN016 Skin Disease 63 0.066
259
CLT003 Colitis 62 0.066
260
P NPH012 Nephrotic Syndrome 60 0.066
261
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.066
262
PRN019 Perinatal Necrotizing Enterocolitis 59 0.066
263
P PYL005 Pyelonephritis 56 0.066
264
HLL004 Hellp Syndrome 54 0.066
265
TXC002 Toxic Encephalopathy 53 0.066
266
P MGR003 Migraine with Aura 52 0.066
267
CYS001 Cystic Fibrosis 81 0.063
268
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.063
269
CRH001 Crohn's Disease 74 0.063
270
P ART022 Arthritis 69 0.063
271
P PNM007 Pneumonia 68 0.063
272
BRN024 Bronchitis 68 0.063
273
HYP056 Hypoglycemia 66 0.063
274
NRM005 Neuromuscular Disease 64 0.063
275
P PRD008 Periodontitis 64 0.063
276
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.063
277
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.063
278
HPT019 Hepatic Encephalopathy 60 0.063
279
GLS018 Glass Syndrome 57 0.063
280
PPT001 Peptic Esophagitis 52 0.063
281
ATN005 Autonomic Dysfunction 46 0.063
282
MYC005 Myocardial Stunning 46 0.063
283
PPL052 Papillomatosis, Confluent and Reticulated 33 0.063
284
BNN005 Bunion 33 0.063
285
ULC004 Ulcerative Colitis 73 0.059
286
P LPR021 Leprosy 3 69 0.059
287
P DRM053 Dermatitis, Atopic 66 0.059
288
KHL003 Kohlschutter-Tonz Syndrome 65 0.059
289
P PTN014 Patent Ductus Arteriosus 1 60 0.059
290
P GST044 Gastritis 56 0.059
291
SNS003 Sensory Peripheral Neuropathy 54 0.059
292
PRP080 Peripheral Artery Disease 53 0.059
293
THY030 Thyroid Gland Disease 52 0.059
294
HYP014 Hyperuricemia 52 0.059
295
BHR001 Behr Syndrome 51 0.059
296
DYS073 Dysphagia 50 0.059
297
CRD137 Cardiogenic Shock 47 0.059
298
RYN005 Raynaud Phenomenon 47 0.059
299
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.059
300
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.059
301
SPR126 Superior Semicircular Canal Dehiscence 40 0.059
302
c HMG029 Hemoglobin Se Disease 39 0.059
303
HNS001 Hansen's Disease 34 0.059
304
MLT131 Multifocal Atrial Tachycardia 18 0.059
305
P HPT023 Hepatocellular Carcinoma 100 0.056
306
CRV035 Cervical Cancer 76 0.056
307
LPT014 Leptin Deficiency or Dysfunction 74 0.056
308
c THR092 Thrombophilia Due to Thrombin Defect 73 0.056
309
P NRB001 Neuroblastoma 72 0.056
310
PRP027 Peripheral Vascular Disease 71 0.056
311
P LYM118 Lymphoma 68 0.056
312
P HPT021 Hepatitis 67 0.056
313
P HYD006 Hydrocephalus 66 0.056
314
P HML002 Hemolytic Anemia 63 0.056
315
P MYL006 Myeloid Leukemia 60 0.056
316
ING001 Inguinal Hernia 60 0.056
317
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.056
318
P INF032 Infertility 57 0.056
319
BLR008 Bilirubin Metabolic Disorder 57 0.056
320
MTH009 Mouth Disease 56 0.056
321
DBT010 Diabetic Neuropathy 54 0.056
322
PRP016 Paraplegia 52 0.056
323
STM007 Stomatitis 50 0.056
324
P MGR001 Migraine Without Aura 49 0.056
325
CRB090 Cerebral Hypoxia 44 0.056
326
IDP073 Idiopathic Hypercalciuria 43 0.056
327
49X006 49, Xxxxy Syndrome 41 0.056
328
c MCR112 Microvascular Complications of Diabetes 2 41 0.056
329
ENT001 Enterocele 39 0.056
330
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.056
331
THR123 Thrombotic Microangiopathy 36 0.056
332
MLD002 Mild Pre-Eclampsia 36 0.056
333
ESP021 Esophageal Cancer 90 0.052
334
c LKM061 Leukemia, Acute Myeloid 84 0.052
335
PLM001 Pulmonary Tuberculosis 69 0.052
336
CNN005 Connective Tissue Disease 68 0.052
337
P NRV007 Nervous System Disease 66 0.052
338
PRT037 Pertussis 65 0.052
339
P ADL010 Adult Respiratory Distress Syndrome 65 0.052
340
P SCL018 Scoliosis 60 0.052
341
IGR001 Ige Responsiveness, Atopic 59 0.052
342
ANR040 Aneurysm 59 0.052
343
P EXN002 Exanthem 57 0.052
344
P PNM006 Pneumoconiosis 56 0.052
345
P GRV001 Graves' Disease 55 0.052
346
END040 Endogenous Depression 55 0.052
347
GTR002 Goiter 53 0.052
348
INT075 Intracranial Hypertension 53 0.052
349
P FBR031 Febrile Seizures 53 0.052
350
NRT001 Neurotic Disorder 53 0.052
351
CHR073 Choreatic Disease 52 0.052
352
OLG003 Oligohydramnios 51 0.052
353
P LCT001 Lactic Acidosis 51 0.052
354
P OVR082 Overgrowth Syndrome 50 0.052
355
PST021 Postpartum Depression 50 0.052
356
ASP007 Aspiration Pneumonia 48 0.052
357
ANT018 Anthracosis 48 0.052
358
WRN003 Wernicke Encephalopathy 47 0.052
359
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.052
360
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.052
361
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.052
362
HYP827 Hypomagnesemia 5, Renal, with or Without Ocular Involvement 44 0.052
363
PPL001 Papillary Adenoma 44 0.052
364
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.052
366
P VSC018 Visceral Steatosis 33 0.052
367
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.052
368
P HYP834 Hypomagnesemia, Seizures, and Mental Retardation 2 22 0.052
369
P LNG032 Lung Cancer 98 0.048
370
P PNC035 Pancreatic Cancer 84 0.048
371
P PRK057 Parkinson Disease, Late-Onset 78 0.048
372
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.048
373
c SPN225 Spondyloarthropathy 1 73 0.048
374
c EXD008 Exudative Vitreoretinopathy 1 71 0.048
375
P HYP061 Hypertrophic Cardiomyopathy 70 0.048
376
ACR008 Acrocallosal Syndrome 69 0.048
377
P OCL013 Oculodentodigital Dysplasia 69 0.048
378
P MYS003 Myasthenia Gravis 68 0.048
379
BRK010 Burkitt Lymphoma 67 0.048
380
c ATS007 Autism Spectrum Disorder 67 0.048
381
P MNN013 Meningitis 66 0.048
382
CLN015 Colon Adenocarcinoma 65 0.048
383
CLR108 Colorectal Adenoma 64 0.048
384
MSC007 Muscle Hypertrophy 64 0.048
385
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.048
386
P NTR004 Neutropenia 63 0.048
387
P INT143 Interstitial Cystitis 61 0.048
388
OST003 Osteonecrosis 61 0.048
389
P ENC004 Encephalitis 61 0.048
390
P SNS001 Sensorineural Hearing Loss 60 0.048
391
CHL014 Cholera 59 0.048
392
THY029 Thyroid Carcinoma 59 0.048
393
GST045 Gastroenteritis 59 0.048
394
P HYP726 Hypercalcemia, Infantile, 1 58 0.048
395
c BNG091 Benign Chronic Pemphigus 58 0.048
396
THY122 Thyroid Gland Cancer 57 0.048
397
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.048
398
P BPL003 Bipolar Disorder 56 0.048
399
PRS047 Prostatitis 56 0.048
400
c GRV008 Graves Disease 1 56 0.048
401
MCS002 Mucositis 56 0.048
402
P MLN007 Male Infertility 55 0.048
403
PRT038 Protein-Energy Malnutrition 54 0.048
404
MYM001 Myoma 54 0.048
405
FRZ001 Frozen Shoulder 53 0.048
406
HRT012 Heart Valve Disease 53 0.048
407
ALC009 Alcoholic Liver Cirrhosis 53 0.048
408
MCN017 Meconium Ileus 52 0.048
409
c VRL010 Viral Hepatitis 52 0.048
410
P CHN059 Chondrocalcinosis 52 0.048
411
P THY032 Thyroiditis 52 0.048
412
HND002 Hand, Foot and Mouth Disease 51 0.048
413
ENT004 Enthesopathy 49 0.048
414
BRS064 Bursitis 48 0.048
415
MGC001 Megacolon 46 0.048
416
P MYC033 Myoclonus 46 0.048
417
SPS057 Spasticity 45 0.048
418
IRT001 Iritis 44 0.048
419
KWS001 Kwashiorkor 44 0.048
420
SNL007 Senile Cataract 42 0.048
421
IDP070 Idiopathic Scoliosis 42 0.048
422
c MJR024 Major Affective Disorder 9 41 0.048
423
PRS063 Paresthesia 41 0.048
424
RDN001 Reading Disorder 40 0.048
425
PLC009 Placenta Praevia 39 0.048
426
c CHR682 Chronic Bilirubin Encephalopathy 39 0.048
427
c MJR022 Major Affective Disorder 8 38 0.048
428
P PRS040 Prostate Cancer 97 0.044
429
P RHM011 Rheumatoid Arthritis 80 0.044
430
BRT054 Brittle Bone Disorder 72 0.044
431
c HPT073 Hepatitis C Virus 72 0.044
432
P GRF003 Graft-Versus-Host Disease 72 0.044
433
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.044
434
ALL003 Allergic Rhinitis 67 0.044
435
P MSC005 Muscular Dystrophy 66 0.044
436
P DYS154 Dystonia 65 0.044
437
BRR014 Barrett Esophagus 65 0.044
438
PRT036 Peritonitis 64 0.044
439
OST017 Osteomyelitis 64 0.044
440
P MVM001 Movement Disease 63 0.044
441
ANR007 Anorexia Nervosa 63 0.044
442
c ALP101 Alpha-Thalassemia 62 0.044
443
c HPT003 Hepatitis a 62 0.044
444
c BRN108 Branchiootic Syndrome 1 62 0.044
445
ATM095 Autoimmune Disease 62 0.044
446
VRL011 Viral Infectious Disease 61 0.044
447
P HMN010 Hemangioma 61 0.044
448
ACQ007 Acquired Immunodeficiency Syndrome 60 0.044
449
LYM027 Lymphopenia 58 0.044
450
P RHN004 Rhinitis 57 0.044
451
HMR039 Hemorrhage, Intracerebral 57 0.044
452
CYT008 Cytomegalovirus Infection 57 0.044
453
PHR003 Pharyngitis 57 0.044
454
BCT022 Bacterial Infectious Disease 56 0.044
455
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.044
456
P MYP006 Myopia 55 0.044
457
ACT058 Active Peptic Ulcer Disease 55 0.044
458
URN010 Urinary Tract Obstruction 55 0.044
459
P RST001 Restless Legs Syndrome 54 0.044
460
HMS001 Hemosiderosis 54 0.044
461
BRN038 Bronchial Disease 53 0.044
462
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.044
463
P PTS002 Ptosis 53 0.044
464
c GLL024 Gallbladder Disease 1 53 0.044
465
PRS030 Persistent Fetal Circulation Syndrome 52 0.044
466
PTH003 Pathologic Nystagmus 52 0.044
467
SPN051 Spondylitis 51 0.044
468
INT071 Intestinal Perforation 51 0.044
469
WRN002 Wernicke-Korsakoff Syndrome 50 0.044
470
PLP001 Pulpitis 49 0.044
471
INT067 Interstitial Nephritis 48 0.044
472
P RNL015 Renal Hypertension 47 0.044
473
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.044
474
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.044
475
SPS007 Spastic Cerebral Palsy 45 0.044
476
CRT015 Carotid Artery Occlusion 45 0.044
477
ASP008 Aspiration Pneumonitis 45 0.044
478
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.044
479
SPN369 Spinal Disease 43 0.044
480
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.044
481
MYF002 Myofascial Pain Syndrome 42 0.044
482
P RRH023 Rare Hereditary Hemochromatosis 41 0.044
483
CRB086 Cerebral Aneurysms 40 0.044
484
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.044
485
c PLY105 Polycystic Ovary Syndrome 1 38 0.044
486
c OVR114 Ovarian Cancer 1 38 0.044
487
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.044
488
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.044
489
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.044
490
P FML187 Familial Hypertension 37 0.044
491
INF009 Inflammatory Spondylopathy 31 0.044
492
c HYP445 Hypomagnesemia 6, Renal 22 0.044
493
c HYP830 Hypomagnesemia, Seizures, and Mental Retardation 1 20 0.044
494
MYL069 Myeloma, Multiple 85 0.040
495
BRN028 Brain Cancer 74 0.040
496
c MNN043 Meningioma, Familial 74 0.040
497
P ALG028 Alagille Syndrome 1 73 0.040
498
P SLP006 Sleep Apnea 69 0.040
499
ART016 Aortic Aneurysm 69 0.040
500
P LKM062 Leukemia, Acute Lymphoblastic 69 0.040
501
OBS002 Obsessive-Compulsive Disorder 68 0.040
502
WLF001 Wolff-Parkinson-White Syndrome 66 0.040
503
P CLC063 Celiac Disease 1 66 0.040
504
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.040
505
c MCL013 Mucolipidosis Iv 66 0.040
506
IRR002 Irritable Bowel Syndrome 65 0.040
507
PLM031 Poliomyelitis 64 0.040
508
P END044 Endometriosis 63 0.040
509
MNN042 Meningioma, Radiation-Induced 62 0.040
510
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.040
511
P LPS004 Lupus Erythematosus 61 0.040
512
TRG002 Trigeminal Neuralgia 60 0.040
513
P OPT006 Optic Nerve Disease 60 0.040
514
PRT013 Portal Hypertension 59 0.040
515
c HPT016 Hepatitis B 59 0.040
516
HLC007 Helicobacter Pylori Infection 59 0.040
517
c ACT073 Acute Leukemia 58 0.040
518
CMP010 Complex Regional Pain Syndrome 58 0.040
519
CHL067 Cholecystitis 57 0.040
520
DSS009 Disseminated Intravascular Coagulation 57 0.040
521
VSC002 Vascular Dementia 57 0.040
522
P MYS005 Myositis 56 0.040
523
ERY051 Erythroleukemia, Familial 56 0.040
524
LMB062 Limb Ischemia 55 0.040
525
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.040
526
P SBS003 Substance Abuse 55 0.040
527
PRP030 Purpura 54 0.040
528
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.040
529
P HMR003 Hemorrhagic Disease 53 0.040
530
HMC014 Homocysteinemia 53 0.040
531
P INT068 Intestinal Disease 53 0.040
532
c CNT035 Central Nervous System Disease 52 0.040
533
DYS015 Dysentery 52 0.040
534
P SPP010 Suppressor of Tumorigenicity 3 51 0.040
535
PLS009 Plasma Cell Neoplasm 51 0.040
536
P RNL007 Renal Tubular Acidosis 51 0.040
537
c HNT004 Huntington Disease-Like 2 50 0.040
538
BRX001 Bruxism 50 0.040
539
SPN021 Spinal Meningioma 50 0.040
540
BLR001 Biliary Atresia 50 0.040
541
ATS010 Autosomal Recessive Disease 48 0.040
542
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.040
543
TST014 Testicular Cancer 46 0.040
544
P HMR005 Hemorrhoid 46 0.040
545
ANR004 Anuria 46 0.040
546
SYN036 Syncope 45 0.040
547
P HYP733 Hypercalciuria, Absorptive, 2 45 0.040
548
ACT003 Acute Kidney Tubular Necrosis 45 0.040
549
RTN179 Retinal Arteries, Tortuosity of 44 0.040
550
PRM003 Premature Ejaculation 44 0.040
551
CVD001 Covid-19 44 0.040
552
IDP033 Idiopathic Edema 44 0.040
553
TRP009 Triple X Syndrome 42 0.040
554
P CLS010 Cluster Headache 42 0.040
555
BCK006 Back Pain 42 0.040
556
SCR001 Secretory Meningioma 41 0.040
557
GLC008 Glucose Metabolism Disease 40 0.040
558
P INT260 Intracranial Berry Aneurysm 39 0.040
559
ANG004 Angioid Streaks 39 0.040
560
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.040
561
TXC001 Toxic Megacolon 38 0.040
562
BLR028 Biliary Atresia, Extrahepatic 37 0.040
563
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.040
564
CRN270 Coronary Artery Dissection, Spontaneous 32 0.040
565
PYR016 Pyridoxine Deficiency 30 0.040
566
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.040
567
MTH071 Methane Production 26 0.040
568
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.040
569
CRB089 Cerebral Beriberi 18 0.040
570
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 17 0.040
571
DGT004 Digitalis Poisoning 14 0.040
572
c SYS001 Systemic Lupus Erythematosus 86 0.034
573
c NRF023 Neurofibromatosis, Type Ii 80 0.034
574
P BLD134 Bladder Cancer 79 0.034
575
SVR004 Severe Combined Immunodeficiency 73 0.034
576
MSC157 Muscular Dystrophy, Duchenne Type 72 0.034
577
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.034
578
P MLN008 Melanoma 69 0.034
579
P ANG001 Angelman Syndrome 69 0.034
580
P SYS005 Systemic Scleroderma 68 0.034
581
P MYC084 Mycobacterium Tuberculosis 1 68 0.034
582
c INF071 Inflammatory Bowel Disease 1 67 0.034
583
APN008 Apnea, Obstructive Sleep 64 0.034
584
GT001 Gout 64 0.034
585
MGK001 Megakaryocytic Leukemia 64 0.034
586
RBR001 Roberts Syndrome 64 0.034
587
c GLC092 Glaucoma, Primary Open Angle 62 0.034
588
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.034
589
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.034
590
P PRM006 Primary Biliary Cirrhosis 62 0.034
591
MSL001 Measles 62 0.034
592
INT002 Intermittent Claudication 61 0.034
593
PNM010 Pneumothorax, Primary Spontaneous 60 0.034
594
P TXP001 Toxoplasmosis 60 0.034
595
ETN001 Eating Disorder 60 0.034
596
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.034
597
SPN027 Spinal Stenosis 59 0.034
598
P INT070 Intestinal Obstruction 58 0.034
599
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.034
600
P GLL020 Gallbladder Disease 57 0.034
601
BRN056 Bronchopulmonary Dysplasia 57 0.034
602
P PRV006 Pervasive Developmental Disorder 57 0.034
603
c LKM070 Leukemia, Acute Monocytic 57 0.034
604
PNM008 Pneumothorax 56 0.034
605
P MLT074 Multiple Endocrine Neoplasia 56 0.034
606
ALL006 Allergic Asthma 56 0.034
607
GNR004 Generalized Anxiety Disorder 56 0.034
608
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.034
609
INT030 Intracranial Aneurysm 56 0.034
610
P PLY019 Polyneuropathy 56 0.034
611
P MYT023 Myotonia Congenita 56 0.034
612
P AGN002 Agnosia 55 0.034
613
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.034
614
ZLL002 Zollinger-Ellison Syndrome 55 0.034
615
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.034
616
SYN007 Synovitis 54 0.034
617
P PMP001 Pemphigus 54 0.034
618
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.034
619
AMN001 Amenorrhea 54 0.034
620
PPL022 Papilloma 54 0.034
621
PRS045 Prostatic Hypertrophy 53 0.034
622
P TCD001 Tic Disorder 53 0.034
623
OCL006 Ocular Hypertension 53 0.034
624
c FML191 Familial Long Qt Syndrome 53 0.034
625
P ACT105 Acute Mountain Sickness 52 0.034
626
ANK001 Ankylosis 51 0.034
627
MYL020 Myelomeningocele 51 0.034
628
P CHL066 Cholangitis 51 0.034
629
ACT017 Acute Chest Syndrome 51 0.034
630
RTN003 Retinal Ischemia 50 0.034
631
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.034
632
P KRT007 Keratoconus 50 0.034
633
PRN009 Paranoid Schizophrenia 50 0.034
634
HMG002 Hemoglobinuria 50 0.034
635
LPR001 Lepromatous Leprosy 50 0.034
636
END021 Endomyocardial Fibrosis 49 0.034
637
P OPN001 Open-Angle Glaucoma 49 0.034
638
GST049 Gastrointestinal System Cancer 49 0.034
639
P RNV001 Renovascular Hypertension 48 0.034
640
SPL018 Splenomegaly 48 0.034
641
BNN003 Bone Inflammation Disease 48 0.034
642
c HYD064 Hydrocephalus, Congenital, 1 48 0.034
643
DRG003 Drug Dependence 47 0.034
644
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.034
645
CRN017 Coronary Thrombosis 47 0.034
646
GST071 Gastrointestinal Carcinoma 47 0.034
647
P CRC039 Coarctation of Aorta 47 0.034
648
CNT033 Central Nervous System Cancer 47 0.034
649
CHR074 Choriocarcinoma 47 0.034
650
LYM019 Lymphosarcoma 46 0.034
651
HYP034 Hypertensive Encephalopathy 46 0.034
652
BCK003 Background Diabetic Retinopathy 46 0.034
653
EXS001 Exostosis 46 0.034
654
KRT013 Keratolytic Winter Erythema 46 0.034
655
PRL008 Paralytic Ileus 45 0.034
656
P PRD021 Periodic Paralysis 45 0.034
657
TNS007 Taeniasis 45 0.034
658
c PRK093 Parkinson Disease 8, Autosomal Dominant 44 0.034
659
MCR011 Microinvasive Gastric Cancer 43 0.034
660
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.034
661
DNT006 Dental Pulp Necrosis 41 0.034
662
PST053 Postherpetic Neuralgia 40 0.034
663
FML039 Female Reproductive System Disease 39 0.034
664
OVR094 Ovarian Epithelial Cancer 38 0.034
665
c CHR098 Chronic Pyelonephritis 38 0.034
666
PLC002 Plica Syndrome 36 0.034
667
PSD088 Pseudobulbar Affect 36 0.034
668
MYT011 Myotonia 34 0.034
669
PRT112 Portal Hypertension, Noncirrhotic 31 0.034
670
CYT004 Cytomegalic Inclusion Disease 31 0.034
671
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 31 0.034
672
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.034
673
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 30 0.034
674
PST092 Posttransplant Acute Limbic Encephalitis 29 0.034
675
TMP019 Temporomandibular Joint Anomaly 28 0.034
676
c PRC045 Preeclampsia/eclampsia 5 25 0.034
677
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.034
678
c PRC034 Preeclampsia/eclampsia 4 23 0.034
679
HML018 Homologous Wasting Disease 22 0.034
680
MGB001 Megabladder, Congenital 18 0.034
681
HYP786 Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy 16 0.034
682
NRL016 Neural Tube Defects 82 0.028
683
MLR004 Malaria 81 0.028
684
PHN003 Phenylketonuria 75 0.028
685
c HMC039 Hemochromatosis, Type 1 74 0.028
686
P MLT020 Multiple Sclerosis 72 0.028
687
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.028
688
OTT002 Otitis Media 72 0.028
689
P AMY004 Amyloidosis 70 0.028
690
GST040 Gastric Adenocarcinoma 70 0.028
691
P FRG001 Fragile X Syndrome 70 0.028
692
c PNC108 Pancreatitis, Hereditary 70 0.028
693
PNC129 Pancreatic Adenocarcinoma 68 0.028
694
P THR014 Thrombocytopenia 67 0.028
695
FCT007 Factor Vii Deficiency 67 0.028
696
GLL008 Gilles De La Tourette Syndrome 66 0.028
697
c SML038 Small Cell Cancer of the Lung 65 0.028
698
P PLM036 Pulmonary Fibrosis 65 0.028
699
P MTR014 Motor Neuron Disease 65 0.028
700
P PRS038 Personality Disorder 65 0.028
701
P THY023 Thymoma 65 0.028
702
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.028
703
TBC004 Tobacco Addiction 64 0.028
704
P FRD001 Friedreich Ataxia 64 0.028
705
TYP007 Typhoid Fever 63 0.028
706
c ACT068 Acute Cystitis 63 0.028
707
P VSC011 Vasculitis 62 0.028
708
LSC001 Lesch-Nyhan Syndrome 62 0.028
709
CRC021 Carcinosarcoma 62 0.028
710
P PRP029 Porphyria 62 0.028
711
WST001 West Syndrome 61 0.028
712
P TST021 Testicular Germ Cell Tumor 60 0.028
713
ACN002 Acanthosis Nigricans 60 0.028
714
SQM006 Squamous Cell Carcinoma 60 0.028
715
ORL011 Oral Cancer 60 0.028
716
INS001 Insulinoma 60 0.028
717
HYD002 Hydronephrosis 60 0.028
718
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.028
719
P GLY013 Glycogen Storage Disease 60 0.028
720
P MYC008 Myocarditis 59 0.028
721
PRT058 Pure Autonomic Failure 59 0.028
722
P PRD006 Prader-Willi Syndrome 59 0.028
723
P LYM033 Lymphoproliferative Syndrome 59 0.028
724
P CYS018 Cystitis 59 0.028
725
AVN001 Avian Influenza 59 0.028
726
P PGT001 Paget's Disease of Bone 58 0.028
727
CNT047 Contact Dermatitis 58 0.028
728
P URT039 Urticaria 58 0.028
729
NWB001 Newborn Respiratory Distress Syndrome 58 0.028
730
EYD002 Eye Disease 58 0.028
731
DSS008 Disease of Mental Health 58 0.028
732
P BNC003 Bone Cancer 58 0.028
733
EXT034 Extrinsic Allergic Alveolitis 58 0.028
734
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 0.028
735
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.028
736
PLC005 Placental Insufficiency 57 0.028
737
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.028
738
P FBR017 Fibrosarcoma 56 0.028
739
PLS011 Plasmacytoma 56 0.028
740
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.028
741
P PSD015 Pseudohypoparathyroidism 56 0.028
742
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.028
743
c BCT007 Bacterial Meningitis 55 0.028
744
P PTT006 Pituitary Adenoma 55 0.028
745
P VNS003 Venous Insufficiency 55 0.028
746
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.028
747
TND005 Tendinitis 54 0.028
748
MMM001 Mammary Paget's Disease 53 0.028
749
PLS016 Plasma Cell Leukemia 53 0.028
750
P HMC002 Homocystinuria 53 0.028
751
P MNC007 Monocytic Leukemia 53 0.028
752
c PRD040 Periodontitis, Chronic 53 0.028
753
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 53 0.028
754
P PNC025 Panic Disorder 53 0.028
755
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.028
756
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.028
757
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.028
758
IMP005 Impotence 52 0.028
759
c THY107 Thymoma, Familial 52 0.028
760
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.028
761
ACT200 Acute Monoblastic Leukemia 52 0.028
762
AVD001 Avoidant Personality Disorder 51 0.028
763
PRS021 Prostatic Adenoma 51 0.028
764
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.028
765
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 51 0.028
766
PRT029 Parathyroid Adenoma 50 0.028
767
c PYR010 Peyronie's Disease 50 0.028
768
PLC008 Placenta Disease 50 0.028
769
P OBS001 Obstructive Jaundice 50 0.028
770
P OTS001 Otosclerosis 49 0.028
771
c CHR418 Chronic Leukemia 49 0.028
772
VLV047 Volvulus of Midgut 49 0.028
773
P MTC133 Mitochondrial Myopathy 49 0.028
774
PRS129 Prostatic Hyperplasia, Benign 49 0.028
775
CCN002 Cocaine Abuse 49 0.028
776
c HPT015 Hepatitis D 49 0.028
777
RFR010 Refractory Anemia 48 0.028
778
ACT098 Acute Erythroid Leukemia 48 0.028
779
P FBR025 Fibrochondrogenesis 48 0.028
780
LPT006 Leptin Receptor Deficiency 48 0.028
781
TBR011 Tuberculous Meningitis 48 0.028
782
VTM002 Vitamin B12 Deficiency 48 0.028
783
KRT008 Keratopathy 47 0.028
784
RNL077 Renal Fibrosis 47 0.028
785
STM006 Stomach Disease 47 0.028
786
RTN020 Retinal Vascular Disease 46 0.028
787
CMP034 Complete Androgen Insensitivity Syndrome 46 0.028
788
DLY008 Delayed Sleep Phase Disorder 46 0.028
789
RCT017 Rectal Disease 46 0.028
790
TCL003 T Cell Deficiency 46 0.028
791
c ACT042 Acute Pyelonephritis 46 0.028
792
GST030 Gastrinoma 45 0.028
793
NWC001 Newcastle Disease 45 0.028
794
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.028
795
ART035 Arterial Calcification of Infancy 45 0.028
796
THR099 Third-Degree Atrioventricular Block 45 0.028
797
JLL001 Jalili Syndrome 45 0.028
798
BLC012 Bile Acid Malabsorption, Primary 45 0.028
799
GRD001 Giardiasis 45 0.028
800
P OST028 Osteochondroma 45 0.028
801
CHP002 Chops Syndrome 44 0.028
802
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.028
803
c PRM038 Primary Agammaglobulinemia 44 0.028
804
MCR017 Macrocytic Anemia 44 0.028
805
CRB016 Carbuncle 43 0.028
806
SDD008 Sudden Sensorineural Hearing Loss 43 0.028
807
DNT001 Dental Fluorosis 43 0.028
808
MDD018 Middle East Respiratory Syndrome 43 0.028
809
ORL015 Oral Squamous Cell Carcinoma 43 0.028
810
P MJR007 Major Affective Disorder 1 43 0.028
811
MRS001 Marasmus 42 0.028
812
P DST107 Distal Renal Tubular Acidosis 42 0.028
813
ORB013 Orbital Disease 42 0.028
814
IDP091 Idiopathic Nephrotic Syndrome 42 0.028
815
c HYP057 Hypervitaminosis D 42 0.028
816
MYS001 Myositis Ossificans 41 0.028
817
ACT088 Acute Insulin Response 41 0.028
818
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.028
819
THR035 Thrombasthenia 40 0.028
820
MDL009 Medullary Sponge Kidney 40 0.028
821
P ADV001 Advanced Sleep Phase Syndrome 40 0.028
822
AMN006 Aminoaciduria 38 0.028
823
TRC005 Tracheal Stenosis 38 0.028
824
c HNT011 Huntington Disease-Like 3 38 0.028
825
SWL001 Swallowing Disorders 38 0.028
826
CRD016 Cardiac Rupture 37 0.028
827
IND003 Indolent Myeloma 36 0.028
828
c HYP302 Hypomagnesemia 4, Renal 36 0.028
829
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.028
830
c AMY088 Amyotrophic Lateral Sclerosis 3 36 0.028
831
ACL001 Acalculous Cholecystitis 35 0.028
832
CHR028 Chronic Wasting Disease 35 0.028
833
c CHR064 Chronic Monocytic Leukemia 33 0.028
834
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.028
835
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.028
836
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.028
837
UTR020 Uterine Inversion 30 0.028
838
c AMY094 Amyotrophic Lateral Sclerosis 5, Juvenile 29 0.028
839
PHS025 Phosphatase, Acid, of Tissues 28 0.028
840
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.028
841
DFF015 Diffuse Glomerulonephritis 26 0.028
842
PRQ002 Paraquat Poisoning 26 0.028
843
ENM002 Enamel Erosion 26 0.028
844
URD002 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to 25 0.028
845
LRY027 Laryngeal Papillomatosis 23 0.028
846
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.028
847
c ADL093 Adult Acute Monocytic Leukemia 20 0.028
848
MNS015 Monosodium Glutamate Sensitivity 20 0.028
849
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.028
851
P RTT002 Rett Syndrome 80 0.020
852
PFF001 Pfeiffer Syndrome 79 0.020
853
INS024 Insulin-Like Growth Factor I 79 0.020
854
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.020
855
MRF001 Marfan Syndrome 77 0.020
856
GLB015 Glioblastoma Multiforme 75 0.020
857
c ART115 Aortic Valve Disease 1 75 0.020
858
ADR007 Adrenoleukodystrophy 75 0.020
859
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.020
860
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.020
861
P HNT016 Huntington Disease 72 0.020
862
c LKM063 Leukemia, Chronic Myeloid 72 0.020
863
ACR007 Acromegaly 71 0.020
864
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.020
865
MYL009 Myelodysplastic Syndrome 70 0.020
866
c GLY008 Glycogen Storage Disease Ii 70 0.020
867
LYM133 Lymphoma, Hodgkin, Classic 69 0.020
868
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.020
869
CHL065 Cholangiocarcinoma 68 0.020
870
SKN019 Skin Melanoma 68 0.020
871
P INF038 Influenza 68 0.020
872
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.020
873
P KBK002 Kabuki Syndrome 1 67 0.020
874
CHR103 Charge Syndrome 67 0.020
875
P HLP001 Holoprosencephaly 67 0.020
876
THY111 Thyroid Carcinoma, Familial Medullary 67 0.020
877
PSY004 Psychotic Disorder 67 0.020
878
FLL027 Fallopian Tube Carcinoma 67 0.020
879
PRT010 Parathyroid Carcinoma 67 0.020
880
LPT001 Leptospirosis 66 0.020
881
P NSP012 Nasopharyngeal Carcinoma 66 0.020
882
AND002 Androgen Insensitivity Syndrome 66 0.020
883
CHG001 Chagas Disease 66 0.020
884
P HRS035 Hirschsprung Disease 1 65 0.020
885
P AGM001 Agammaglobulinemia 65 0.020
886
P CNJ013 Conjunctivitis 65 0.020
887
SRC014 Sarcoma 65 0.020
888
P MTR004 Maturity-Onset Diabetes of the Young 65 0.020
889
GRN037 Granulomatosis with Polyangiitis 65 0.020
890
P GLC113 Galactosemia I 64 0.020
891
ART002 Arts Syndrome 64 0.020
892
PRP083 Porphyria, Acute Intermittent 64 0.020
893
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.020
894
LYM017 Lyme Disease 64 0.020
895
HYP020 Hyperprolactinemia 64 0.020
896
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.020
897
KRN002 Kearns-Sayre Syndrome 63 0.020
898
LSH001 Leishmaniasis 63 0.020
899
P ANR048 Aniridia 1 63 0.020
900
PLG002 Plague 63 0.020
901
c HYP794 Hyperoxaluria, Primary, Type I 63 0.020
902
P PTT014 Pitt-Hopkins Syndrome 63 0.020
903
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.020
904
TRN015 Transient Cerebral Ischemia 63 0.020
905
c ATM011 Autoimmune Hepatitis 63 0.020
906
c LCL006 Localized Scleroderma 62 0.020
907
HMT002 Hematologic Cancer 62 0.020
908
c HPT001 Hepatitis C 62 0.020
909
P PLY014 Polycystic Kidney Disease 62 0.020
910
P PSR002 Psoriasis 62 0.020
911
P MCH002 Machado-Joseph Disease 62 0.020
912
c SVR001 Severe Acute Respiratory Syndrome 62 0.020
913
P DNT020 Dent Disease 1 62 0.020
914
P TRC086 Trichohepatoenteric Syndrome 1 62 0.020
915
P PRM002 Primary Hyperoxaluria 62 0.020
916
HSH003 Hashimoto Thyroiditis 62 0.020
917
P CRN108 Cranioectodermal Dysplasia 1 62 0.020
918
P DRM010 Dermatomyositis 61 0.020
919
PSR001 Psoriatic Arthritis 61 0.020
920
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.020
921
c SCL052 Scleroderma, Familial Progressive 61 0.020
922
c WLM018 Wilms Tumor 5 61 0.020
923
WHM001 Whim Syndrome 61 0.020
924
APP008 Appendicitis 61 0.020
925
NRL005 Neurilemmoma 60 0.020
926
P KDN017 Kidney Cancer 60 0.020
927
HRP004 Herpes Zoster 60 0.020
928
P ALP009 Alopecia Areata 60 0.020
929
STR039 Sturge-Weber Syndrome 60 0.020
930
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.020
931
RHM001 Rheumatic Fever 60 0.020
932
VRC005 Varicose Veins 60 0.020
933
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.020
934
P BRN019 Bernard-Soulier Syndrome 60 0.020
935
P AXN002 Axenfeld-Rieger Syndrome 59 0.020
936
P MCR010 Microcephaly 59 0.020
937
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 59 0.020
938
CHL123 Chlamydia 59 0.020
939
PLM033 Pulmonary Embolism 59 0.020
940
GNG013 Gingivitis 59 0.020
941
IRN001 Iron Deficiency Anemia 59 0.020
942
P NMN002 Niemann-Pick Disease 59 0.020
943
ALP097 Alopecia Universalis Congenita 59 0.020
944
P SYP003 Syphilis 58 0.020
945
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.020
946
ANT024 Anthrax Disease 58 0.020
947
PST028 Post-Traumatic Stress Disorder 58 0.020
948
ERY029 Erythermalgia, Primary 58 0.020
949
P BCL017 B-Cell Lymphoma 58 0.020
950
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.020
951
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 58 0.020
952
P MTR012 Mitral Valve Disease 58 0.020
953
CHL028 Childhood Type Dermatomyositis 58 0.020
954
c DWL002 Dowling-Degos Disease 1 58 0.020
955
P GLL018 Gallbladder Cancer 57 0.020
956
P PLV020 Pelvic Organ Prolapse 57 0.020
957
c VSC019 Vesicoureteral Reflux 1 57 0.020
958
CPR004 Coproporphyria, Hereditary 57 0.020
959
P PRN023 Prion Disease 57 0.020
960
c MST023 Mesothelioma, Malignant 57 0.020
961
P FCL005 Focal Segmental Glomerulosclerosis 57 0.020
962
TNS005 Tonsillitis 57 0.020
963
APH002 Aphasia 57 0.020
964
CMM005 Common Cold 57 0.020
965
SCH014 Schistosomiasis 57 0.020
966
AYM001 Ayme-Gripp Syndrome 57 0.020
967
PGM001 Pigmented Villonodular Synovitis 56 0.020
968
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.020
969
TCK001 Tick-Borne Encephalitis 56 0.020
970
c ACT134 Acute Liver Failure 56 0.020
971
SCH003 Schizophreniform Disorder 56 0.020
972
ALL010 Allergic Contact Dermatitis 56 0.020
973
EMB004 Embryonal Carcinoma 56 0.020
974
c FML035 Familial Hyperlipidemia 55 0.020
975
MCN007 Meconium Aspiration Syndrome 55 0.020
976
P SCK002 Sick Sinus Syndrome 55 0.020
977
MCL006 Macular Retinal Edema 55 0.020
978
ORL004 Oral Submucous Fibrosis 55 0.020
979
c PRG126 Progressive Familial Heart Block 55 0.020
980
NRG002 Neurogenic Bladder 55 0.020
981
c OST135 Osteogenesis Imperfecta, Type I 55 0.020
982
AMB001 Amebiasis 55 0.020
983
MMB001 Membranoproliferative Glomerulonephritis 55 0.020
984
VSC003 Visceral Leishmaniasis 55 0.020
985
P ANT006 Antiphospholipid Syndrome 55 0.020
986
RNL051 Renal Cysts and Diabetes Syndrome 55 0.020
987
HDR002 Hidradenitis Suppurativa 55 0.020
988
c MYP132 Myopathy, Congenital 55 0.020
989
P DBT005 Diabetes Insipidus 55 0.020
990
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.020
991
P LRY044 Larynx Cancer 55 0.020
992
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.020
993
TRD006 Tardive Dyskinesia 54 0.020
994
AMN003 Amnestic Disorder 54 0.020
995
CRT017 Cartilage Disease 54 0.020
996
P FML068 Familial Hypocalciuric Hypercalcemia 54 0.020
997
P ALP008 Alopecia 54 0.020
998
FCL014 Focal Epilepsy 54 0.020
999
GST037 Gastroparesis 54 0.020
1000
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.020
1001
P ICH004 Ichthyosis 54 0.020
1002
BRN014 Bronchopneumonia 54 0.020
1003
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.020
1004
THR013 Thoracic Outlet Syndrome 54 0.020
1005
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.020
1006
CLL003 Cellulitis 54 0.020
1007
c HNT010 Huntington Disease-Like 1 53 0.020
1008
TRC023 Trichinosis 53 0.020
1009
HYP706 Hypermobile Ehlers-Danlos Syndrome 53 0.020
1010
RHM028 Rheumatic Heart Disease 53 0.020
1011
P FML023 Familial Hemiplegic Migraine 53 0.020
1012
CRH005 Crohn's Colitis 53 0.020
1013
P RTN016 Retinal Degeneration 53 0.020
1014
MST005 Mastitis 53 0.020
1015
P GRS003 Griscelli Syndrome 53 0.020
1016
MTN003 Motion Sickness 53 0.020
1017
c XNT010 Xanthinuria, Type I 53 0.020
1018
NNT012 Neonatal Jaundice 53 0.020
1019
P RTN018 Retinal Disease 53 0.020
1020
CLB010 Coloboma of Macula 52 0.020
1021
NRT004 Neuritis 52 0.020
1022
PST011 Pustulosis of Palm and Sole 52 0.020
1023
ART074 Aortic Dissection 52 0.020
1024
c LYM114 Lymphoproliferative Syndrome, X-Linked, 2 52 0.020
1025
TLN003 Telangiectasis 52 0.020
1026
P TRT010 Teratoma 52 0.020
1027
P HMP007 Hemophilia 51 0.020
1028
THR004 Thrombocytosis 51 0.020
1029
c ART120 Arthrogryposis, Distal, Type 3 51 0.020
1030
CLR109 Colorectal Adenocarcinoma 51 0.020
1031
c PNC106 Pancreatic Agenesis 1 51 0.020
1032
THR016 Thrombophlebitis 51 0.020
1033
INT079 Intrahepatic Cholangiocarcinoma 51 0.020
1034
LNG031 Lung Benign Neoplasm 51 0.020
1035
CCC002 Coccidiosis 51 0.020
1036
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.020
1037
P AST007 Astrocytoma 51 0.020
1038
TLR001 Tularemia 51 0.020
1039
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.020
1040
HYP081 Hypolipoproteinemia 51 0.020
1041
SCH012 Schizoaffective Disorder 50 0.020
1042
PLR007 Pleural Empyema 50 0.020
1043
RDC002 Radiculopathy 50 0.020
1044
ALL009 Allergic Conjunctivitis 50 0.020
1045
RSP006 Respiratory System Disease 50 0.020
1046
CRN030 Coronary Stenosis 50 0.020
1047
BRN009 Burning Mouth Syndrome 50 0.020
1048
P MTR003 Mitral Valve Stenosis 50 0.020
1049
AZS001 Azoospermia 50 0.020
1050
c HRD202 Hereditary Lymphedema I 50 0.020
1051
THY125 Thyroid Gland Medullary Carcinoma 50 0.020
1052
c INF145 Infantile Liver Failure Syndrome 1 50 0.020
1053
TRY001 Trypanosomiasis 50 0.020
1054
SLR001 Sialuria 50 0.020
1055
LSS003 Lassa Fever 50 0.020
1056
NPH010 Nephrosclerosis 50 0.020
1057
OPT003 Opiate Dependence 50 0.020
1058
DBT004 Diabetic Polyneuropathy 49 0.020
1059
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.020
1060
ONC007 Oncocytoma 49 0.020
1061
c CHR431 Chronic Venous Insufficiency 49 0.020
1062
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.020
1063
HYP006 Hypertensive Heart Disease 49 0.020
1064
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.020
1065
VRC001 Varicocele 49 0.020
1066
LFT001 Left Bundle Branch Hemiblock 49 0.020
1067
P END046 Endometritis 49 0.020
1068
HDR003 Hidradenitis 49 0.020
1069
CMB003 Combined T Cell and B Cell Immunodeficiency 49 0.020
1070
INT078 Intracranial Thrombosis 49 0.020
1071
CHL004 Cholelithiasis 49 0.020
1072
P CRV031 Cervical Adenocarcinoma 49 0.020
1073
P SDR003 Sideroblastic Anemia 49 0.020
1074
DNT045 Dental Anomalies and Short Stature 49 0.020
1075
BCT004 Bacteriuria 49 0.020
1076
VCC001 Vaccinia 49 0.020
1077
LRN003 Learning Disability 49 0.020
1078
QDR001 Quadriplegia 48 0.020
1079