Search results for Magnesium

966 hits were found for Magnesium

# Family MCID Name MIFTS Score
1
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 36 9.271
2
P HYP210 Hypomagnesemia 2, Renal 34 7.677
3
HYP550 Hypomagnesemia 1, Intestinal 38 4.111
4
GTL001 Gitelman Syndrome 62 4.075
5
c HYP534 Hypomagnesemia 3, Renal 37 3.336
6
MGN003 Magnesium, Elevated Red Cell 5 2.349
7
P ECL001 Eclampsia 58 0.321
8
c PRC016 Pre-Eclampsia 61 0.300
9
PNG002 Pain Agnosia 54 0.257
10
c SVR005 Severe Pre-Eclampsia 55 0.203
11
PLC008 Placenta Disease 59 0.201
12
AST005 Asthma 81 0.191
13
c PRC031 Preeclampsia/eclampsia 1 41 0.173
14
GST050 Gastrointestinal System Disease 67 0.168
15
P KDN018 Kidney Disease 71 0.167
16
LNG099 Lung Disease 70 0.167
17
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.165
18
P ENC018 Encephalopathy 65 0.164
19
ISC004 Ischemia 67 0.159
20
P DBT009 Diabetes Mellitus 67 0.154
21
P HRT032 Heart Disease 76 0.142
22
P LVR013 Liver Disease 76 0.138
23
c CHR089 Chronic Kidney Failure 73 0.134
24
ISC006 Ischemic Heart Disease 72 0.134
25
c CNT035 Central Nervous System Disease 65 0.134
26
VSC007 Vascular Disease 72 0.132
27
CRB037 Cerebral Palsy 71 0.132
28
GST092 Gastroesophageal Reflux 66 0.132
29
P INT068 Intestinal Disease 62 0.132
30
BRN038 Bronchial Disease 58 0.130
31
P NRV007 Nervous System Disease 71 0.128
32
BRN071 Brain Injury 55 0.128
33
RSP006 Respiratory System Disease 64 0.126
34
P CRN300 Coronary Heart Disease 1 61 0.126
35
URN009 Urinary System Disease 59 0.126
36
HYP005 Hypokalemia 55 0.124
37
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.124
38
NPH003 Nephrocalcinosis 50 0.120
39
DPR016 Depression 72 0.118
40
CRB039 Cerebrovascular Disease 70 0.118
41
HDC001 Headache 62 0.118
42
P CLR023 Colorectal Cancer 99 0.116
43
P MYC007 Myocardial Infarction 78 0.116
44
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.116
45
ART140 Arteries, Anomalies of 66 0.116
46
P NRP001 Neuropathy 63 0.116
47
GST049 Gastrointestinal System Cancer 62 0.116
48
GST071 Gastrointestinal Carcinoma 45 0.116
49
P CRN018 Coronary Artery Anomaly 75 0.114
50
NTR005 Nutritional Deficiency Disease 59 0.114
51
CLC006 Calcinosis 53 0.114
52
P ATR011 Atrial Fibrillation 69 0.111
53
TTN003 Tetanus 66 0.111
54
ESP023 Esophageal Disease 59 0.111
55
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.111
56
DYS073 Dysphagia 48 0.109
57
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 63 0.107
58
c LRG017 Large Intestine Cancer 63 0.107
59
CLN019 Colonic Disease 62 0.107
60
P ESP024 Esophagitis 60 0.107
61
CRD223 Cardiac Arrhythmia 55 0.107
62
SPS003 Spastic Diplegia 55 0.107
63
P BRS047 Breast Cancer 100 0.104
64
GST045 Gastroenteritis 65 0.104
65
P ART021 Arteriosclerosis 61 0.104
66
P DRR001 Diarrhea 58 0.104
67
P HYP024 Hypoparathyroidism 55 0.104
68
RCT017 Rectal Disease 43 0.104
69
SWL001 Swallowing Disorders 36 0.104
70
CNS004 Constipation 58 0.102
71
INT253 Intestinal Benign Neoplasm 57 0.102
72
HDN002 Head Injury 52 0.102
73
ISL119 Isolated Optic Neuritis 34 0.102
74
FTT001 Fatty Liver Disease 66 0.099
75
BND020 Bone Disease 64 0.099
76
P MYP004 Myopathy 64 0.099
77
STT002 Status Asthmaticus 46 0.099
78
c HYP595 Hypertension, Essential 81 0.096
79
P OST002 Osteoporosis 74 0.096
80
P PRP019 Peripheral Nervous System Disease 66 0.096
81
P HML002 Hemolytic Anemia 64 0.096
82
GST033 Gestational Diabetes 63 0.096
83
END030 End Stage Renal Failure 60 0.096
85
SCK003 Sickle Cell Anemia 74 0.094
86
ANX010 Anxiety 73 0.094
87
MNT002 Mental Depression 65 0.094
88
ADN018 Adenoma 64 0.094
89
DYS011 Dyskinesia of Esophagus 42 0.094
90
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 61 0.091
91
NRM005 Neuromuscular Disease 61 0.091
92
NRT004 Neuritis 58 0.091
93
c ACT075 Acute Myocardial Infarction 57 0.091
94
SCK005 Sickle Cell Disease 57 0.091
95
P MSC033 Muscle Disorders 57 0.091
96
P NNL004 Nonalcoholic Fatty Liver Disease 56 0.091
97
HYP025 Hyperphosphatemia 49 0.091
98
PRM237 Primary Hypomagnesemia 39 0.091
99
CNG034 Congestive Heart Failure 70 0.088
100
c MGR028 Migraine with or Without Aura 1 69 0.088
101
HYP266 Hypoxia 63 0.088
102
SDD001 Sudden Infant Death Syndrome 62 0.088
103
BRN004 Brain Edema 59 0.088
104
TRM010 Traumatic Brain Injury 56 0.088
105
STM006 Stomach Disease 55 0.088
106
ENT011 Enterocolitis 54 0.088
107
HMG005 Hemoglobinopathy 54 0.088
108
MSC190 Muscular Disease 53 0.088
109
c CNG027 Congenital Hemolytic Anemia 53 0.088
110
MSC004 Muscle Tissue Disease 39 0.088
111
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.088
112
ADG002 Audiogenic Seizures 26 0.088
113
OST012 Osteoarthritis 80 0.085
114
P LKM002 Leukemia 72 0.085
115
P ADN016 Adenocarcinoma 70 0.085
116
P PLY011 Polycystic Ovary Syndrome 64 0.085
117
PPT005 Peptic Ulcer Disease 63 0.085
118
PRN019 Perinatal Necrotizing Enterocolitis 58 0.085
119
NPH009 Nephrolithiasis 58 0.085
120
PRM020 Premenstrual Tension 53 0.085
121
P BLD051 Blood Coagulation Disease 52 0.085
122
c PNC128 Pain - Chronic 49 0.085
123
BNF002 Bone Fracture 48 0.085
124
P HYP265 Hypotonia 43 0.085
125
INT323 Intraocular Pressure Quantitative Trait Locus 38 0.085
126
c TRC078 Trichohepatoenteric Syndrome 2 35 0.085
127
THR024 Thrombosis 64 0.082
128
BRN002 Bronchiolitis 61 0.082
129
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.082
130
SLP005 Sleep Disorder 60 0.082
131
PLM010 Pulmonary Edema 59 0.082
132
P VSC018 Visceral Steatosis 37 0.082
133
LVR012 Liver Cirrhosis 67 0.079
134
THR100 Thrombocytopenic Purpura, Autoimmune 67 0.079
135
TXC005 Toxic Shock Syndrome 62 0.079
136
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 62 0.079
137
HYP060 Hyperinsulinism 57 0.079
138
BNR002 Bone Resorption Disease 54 0.079
139
DDN027 Duodenum Disease 43 0.079
140
P EPL164 Epilepsy 72 0.075
141
P HYP086 Hypothyroidism 66 0.075
142
P CRD132 Cardiac Conduction Defect 63 0.075
143
TXC002 Toxic Encephalopathy 57 0.075
144
PRV004 Periventricular Leukomalacia 49 0.075
145
c BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.075
146
LKM006 Leukomalacia 41 0.075
147
STR067 Stroke, Ischemic 82 0.072
148
P ORT004 Orthostatic Intolerance 69 0.072
149
VRL011 Viral Infectious Disease 68 0.072
150
P PSD087 Pseudoxanthoma Elasticum 68 0.072
151
LPD008 Lipid Metabolism Disorder 65 0.072
152
MTH009 Mouth Disease 64 0.072
153
P SZR006 Seizure Disorder 61 0.072
154
PHR003 Pharyngitis 58 0.072
155
GLC008 Glucose Metabolism Disease 53 0.072
156
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 48 0.072
157
BRN080 Brain Ischemia 43 0.072
158
P HPT021 Hepatitis 73 0.068
159
P RSP003 Respiratory Failure 72 0.068
160
SKN016 Skin Disease 68 0.068
161
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.068
162
FBR047 Fibromyalgia 66 0.068
163
P CRD119 Cardiac Arrest 66 0.068
164
P TRC086 Trichohepatoenteric Syndrome 1 60 0.068
165
CHL068 Cholestasis 60 0.068
166
P INF032 Infertility 60 0.068
167
BRN106 Burns 59 0.068
168
END035 Endocrine Gland Cancer 57 0.068
169
DYS014 Dyspepsia 56 0.068
170
PLC007 Placental Abruption 51 0.068
171
P DDN001 Duodenal Ulcer 51 0.068
172
P ALZ034 Alzheimer Disease 87 0.064
173
P PLM037 Pulmonary Hypertension 77 0.064
174
P PHC003 Pheochromocytoma 72 0.064
175
P LYM118 Lymphoma 69 0.064
176
P ART023 Arthropathy 68 0.064
177
CNN005 Connective Tissue Disease 67 0.064
178
BRS051 Breast Disease 66 0.064
179
c ACT210 Acute Respiratory Distress Syndrome 66 0.064
180
P LNG028 Long Qt Syndrome 66 0.064
181
MDD011 Mood Disorder 65 0.064
182
CLT003 Colitis 65 0.064
183
HYP066 Hyperglycemia 64 0.064
184
P THR014 Thrombocytopenia 64 0.064
185
JNT002 Joint Disorders 64 0.064
186
P PNC044 Pancreatitis 62 0.064
187
PNC034 Pancreas Disease 59 0.064
188
SNS003 Sensory Peripheral Neuropathy 56 0.064
189
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 55 0.064
190
c ACT071 Acute Kidney Failure 54 0.064
191
NNL002 Nonalcoholic Steatohepatitis 54 0.064
192
CHR005 Chorioamnionitis 53 0.064
193
c PNC106 Pancreatic Agenesis 1 51 0.064
194
P BRB001 Beriberi 46 0.064
195
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 34 0.064
196
GST053 Gastric Cancer 78 0.060
197
P ART022 Arthritis 77 0.060
198
PSY004 Psychotic Disorder 74 0.060
199
PRP027 Peripheral Vascular Disease 72 0.060
200
BRN028 Brain Cancer 72 0.060
201
P PNM007 Pneumonia 72 0.060
202
BRN024 Bronchitis 70 0.060
203
DMN002 Dementia 69 0.060
204
P MYL006 Myeloid Leukemia 67 0.060
205
P SBS003 Substance Abuse 60 0.060
206
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.060
207
P PNS012 Paine Syndrome 60 0.060
208
P MLG056 Malignant Hyperthermia 60 0.060
209
P RST001 Restless Legs Syndrome 59 0.060
210
P HYP069 Hyperparathyroidism 59 0.060
211
P HMR003 Hemorrhagic Disease 59 0.060
212
P SCL018 Scoliosis 58 0.060
213
c MCR113 Microvascular Complications of Diabetes 3 58 0.060
214
P THR015 Thrombophilia 56 0.060
215
PRP080 Peripheral Artery Disease 56 0.060
216
OVR063 Overnutrition 53 0.060
217
URM002 Uremia 53 0.060
218
BLR006 Biliary Tract Disease 52 0.060
219
P SHR001 Short Bowel Syndrome 52 0.060
220
P BLD036 Bile Duct Disease 51 0.060
221
MTB004 Metabolic Acidosis 50 0.060
222
c MTR002 Mitral Valve Insufficiency 50 0.060
223
TRP008 Tropical Calcific Pancreatitis 50 0.060
224
ADR040 Adrenal Gland Pheochromocytoma 49 0.060
225
c MCR120 Microvascular Complications of Diabetes 7 46 0.060
226
HPT004 Hepatic Coma 45 0.060
227
PRS063 Paresthesia 45 0.060
228
c MCR130 Microvascular Complications of Diabetes 6 43 0.060
229
c MCR133 Microvascular Complications of Diabetes 4 43 0.060
230
VSC008 Vascular Hemostatic Disease 43 0.060
231
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.060
232
BNN005 Bunion 34 0.060
233
BLD165 Blood Group, Colton System 34 0.060
234
HYP827 Hypomagnesemia 5, Renal, with or Without Ocular Involvement 29 0.060
235
RPD005 Rapidly Involuting Congenital Hemangioma 25 0.060
236
c HYP834 Hypomagnesemia, Seizures, and Mental Retardation 2 16 0.060
237
P OVR042 Ovarian Cancer 83 0.056
238
c LKM061 Leukemia, Acute Myeloid 81 0.056
239
P INF038 Influenza 75 0.056
240
c BTT014 Beta-Thalassemia 72 0.056
241
P ALC004 Alcohol Abuse 68 0.056
242
P ATS364 Autism 67 0.056
243
ACQ007 Acquired Immunodeficiency Syndrome 66 0.056
244
SPN186 Spinal Cord Injury 66 0.056
245
P THL005 Thalassemia 65 0.056
246
P OVR049 Ovarian Disease 63 0.056
247
ERY003 Erythema Multiforme 62 0.056
248
GT001 Gout 62 0.056
249
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.056
250
GST023 Gastric Ulcer 58 0.056
251
MCN017 Meconium Ileus 56 0.056
252
WRN002 Wernicke-Korsakoff Syndrome 52 0.056
253
THY030 Thyroid Gland Disease 50 0.056
254
FSH001 Fish-Eye Disease 50 0.056
255
WTH001 Withdrawal Disorder 50 0.056
256
GND003 Gonadal Disease 49 0.056
257
HRT008 Heart Conduction Disease 44 0.056
258
c PLY105 Polycystic Ovary Syndrome 1 42 0.056
259
IDP070 Idiopathic Scoliosis 40 0.056
260
ENC005 Encephalomalacia 40 0.056
261
ACT118 Acute Non Lymphoblastic Leukemia 32 0.056
262
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 32 0.056
263
P PRS040 Prostate Cancer 93 0.051
264
ULC004 Ulcerative Colitis 80 0.051
265
P SCH015 Schizophrenia 73 0.051
266
P DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.051
267
THY028 Thyroid Cancer 72 0.051
268
DSS008 Disease of Mental Health 71 0.051
269
BRR014 Barrett Esophagus 70 0.051
270
ALC007 Alcohol Dependence 69 0.051
271
ALL026 Allergic Hypersensitivity Disease 68 0.051
272
P PRD008 Periodontitis 66 0.051
273
RCK004 Rickets 66 0.051
274
RHM027 Rheumatic Disease 65 0.051
275
P ADL010 Adult Respiratory Distress Syndrome 64 0.051
276
MGK001 Megakaryocytic Leukemia 64 0.051
277
AGN016 Aging 63 0.051
278
SPP010 Suppressor of Tumorigenicity 3 60 0.051
279
MCS002 Mucositis 60 0.051
280
IRN002 Iron Metabolism Disease 60 0.051
281
HPT019 Hepatic Encephalopathy 60 0.051
282
NWB001 Newborn Respiratory Distress Syndrome 59 0.051
283
GLC003 Glucose Intolerance 59 0.051
284
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 59 0.051
285
P RCT021 Rectum Cancer 58 0.051
286
P MNC007 Monocytic Leukemia 58 0.051
287
CLN015 Colon Adenocarcinoma 57 0.051
288
c LKM070 Leukemia, Acute Monocytic 57 0.051
289
P INF037 Inflammatory Bowel Disease 56 0.051
290
HND002 Hand, Foot and Mouth Disease 56 0.051
291
PRT082 Preterm Premature Rupture of the Membranes 55 0.051
292
P INT070 Intestinal Obstruction 55 0.051
293
c SCN007 Secondary Hyperparathyroidism 55 0.051
294
BLR008 Bilirubin Metabolic Disorder 54 0.051
295
ACT058 Active Peptic Ulcer Disease 53 0.051
296
P CLL015 Collagen Disease 52 0.051
297
ACT098 Acute Erythroid Leukemia 51 0.051
298
SKN027 Skin Conditions 51 0.051
299
ACT200 Acute Monoblastic Leukemia 49 0.051
300
WRN003 Wernicke Encephalopathy 49 0.051
301
ACT017 Acute Chest Syndrome 48 0.051
302
IDP073 Idiopathic Hypercalciuria 48 0.051
303
CRB004 Cerebral Artery Occlusion 47 0.051
304
SPN369 Spinal Disease 47 0.051
305
KWS001 Kwashiorkor 46 0.051
306
SPS057 Spasticity 44 0.051
307
ACT113 Acute Myeloblastic Leukemia with Maturation 43 0.051
308
MYF002 Myofascial Pain Syndrome 43 0.051
309
BWN003 Bowenoid Papulosis 42 0.051
310
OVR094 Ovarian Epithelial Cancer 41 0.051
311
SCR035 Sacral Agenesis with Vertebral Anomalies 41 0.051
312
RCT020 Rectum Adenocarcinoma 40 0.051
313
PRL008 Paralytic Ileus 40 0.051
314
PHS001 Phosphorus Metabolism Disease 40 0.051
315
RSP007 Respiratory Distress Syndrome, Infant 37 0.051
316
ACT114 Acute Myeloblastic Leukemia Without Maturation 32 0.051
317
c ADL093 Adult Acute Monocytic Leukemia 22 0.051
318
P HYP830 Hypomagnesemia, Seizures, and Mental Retardation 1 20 0.051
319
c HYP445 Hypomagnesemia 6, Renal 19 0.051
320
ACT096 Acute Cholinergic Dysautonomia 19 0.051
321
P PNC035 Pancreatic Cancer 82 0.045
322
CRV035 Cervical Cancer 76 0.045
323
ACR006 Aceruloplasminemia 73 0.045
324
c EXD008 Exudative Vitreoretinopathy 1 72 0.045
325
LPT014 Leptin Deficiency or Dysfunction 70 0.045
326
P ALG028 Alagille Syndrome 1 70 0.045
327
c HPT016 Hepatitis B 70 0.045
328
ANG054 Angina Pectoris 69 0.045
329
c ATS007 Autism Spectrum Disorder 67 0.045
330
P MJR001 Major Depressive Disorder 67 0.045
331
c HPT003 Hepatitis a 66 0.045
332
HYP056 Hypoglycemia 64 0.045
333
CYT008 Cytomegalovirus Infection 62 0.045
334
HMR039 Hemorrhage, Intracerebral 62 0.045
335
P PTN014 Patent Ductus Arteriosus 1 61 0.045
336
P GST044 Gastritis 60 0.045
337
P NTR004 Neutropenia 60 0.045
338
P NRV006 Nervous System Cancer 60 0.045
339
STT001 Status Epilepticus 60 0.045
340
TRG002 Trigeminal Neuralgia 60 0.045
341
P LRY044 Larynx Cancer 60 0.045
342
BRN056 Bronchopulmonary Dysplasia 60 0.045
343
P SNS001 Sensorineural Hearing Loss 60 0.045
344
END040 Endogenous Depression 59 0.045
345
c MCL013 Mucolipidosis Iv 58 0.045
346
DSS009 Disseminated Intravascular Coagulation 58 0.045
347
RTN018 Retinal Disease 58 0.045
348
IMM136 Immune System Disease 57 0.045
349
INT075 Intracranial Hypertension 57 0.045
350
PRV006 Pervasive Developmental Disorder 56 0.045
351
PST021 Postpartum Depression 56 0.045
352
P TRM003 Tremor 55 0.045
353
BLR001 Biliary Atresia 55 0.045
354
P PTS002 Ptosis 55 0.045
355
c BNG091 Benign Chronic Pemphigus 54 0.045
356
PRT038 Protein-Energy Malnutrition 53 0.045
357
LYM019 Lymphosarcoma 53 0.045
358
P LCT001 Lactic Acidosis 52 0.045
359
P OVR046 Ovarian Cyst 52 0.045
360
GRN017 Granulocytopenia 51 0.045
361
CHR073 Choreatic Disease 50 0.045
362
PLP001 Pulpitis 50 0.045
363
RNL011 Renal Osteodystrophy 49 0.045
364
EPD070 Epidermoid Cysts 48 0.045
365
SPS007 Spastic Cerebral Palsy 48 0.045
366
DCB001 Decubitus Ulcer 47 0.045
367
CRB086 Cerebral Aneurysms 45 0.045
368
CLN044 Colon Adenoma 43 0.045
369
BRN014 Bronchopneumonia 43 0.045
370
CRB085 Cerebral Hemorrhage 42 0.045
371
FXF002 Fox-Fordyce Disease 40 0.045
372
PLC009 Placenta Praevia 39 0.045
373
RNL021 Renal Tubular Transport Disease 38 0.045
374
MLD002 Mild Pre-Eclampsia 37 0.045
375
OST097 Osteoporotic Fracture 36 0.045
376
BLR028 Biliary Atresia, Extrahepatic 33 0.045
378
CRC034 Carcinoma Showing Thymus-Like Differentiation 28 0.045
379
ELS005 Elastoma 24 0.045
380
CRB089 Cerebral Beriberi 22 0.045
381
MYL069 Myeloma, Multiple 85 0.039
382
ESP021 Esophageal Cancer 82 0.039
383
c SPN225 Spondyloarthropathy 1 75 0.039
384
P MLT020 Multiple Sclerosis 75 0.039
385
P MCR115 Microvascular Complications of Diabetes 5 70 0.039
386
P SLP006 Sleep Apnea 70 0.039
387
BRT054 Brittle Bone Disorder 70 0.039
388
BRK010 Burkitt Lymphoma 69 0.039
389
P MNN013 Meningitis 69 0.039
390
c THR092 Thrombophilia Due to Thrombin Defect 69 0.039
391
APN008 Apnea, Obstructive Sleep 68 0.039
392
PRT036 Peritonitis 66 0.039
393
OST159 Osteogenic Sarcoma 66 0.039
394
DFC004 Deficiency Anemia 66 0.039
395
P VSC011 Vasculitis 66 0.039
396
HLC007 Helicobacter Pylori Infection 65 0.039
397
STF001 Stiff-Person Syndrome 64 0.039
398
MYL031 Myeloproliferative Neoplasm 64 0.039
399
P LYM033 Lymphoproliferative Syndrome 63 0.039
400
CMP010 Complex Regional Pain Syndrome 63 0.039
401
PRM236 Primary Biliary Cholangitis 63 0.039
402
BCT022 Bacterial Infectious Disease 62 0.039
403
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 62 0.039
404
P THR005 Thrombotic Thrombocytopenic Purpura 62 0.039
405
PLS011 Plasmacytoma 62 0.039
406
ING001 Inguinal Hernia 61 0.039
407
P GRV001 Graves' Disease 61 0.039
408
ATH013 Atherosclerosis Susceptibility 60 0.039
409
P UTR058 Uterine Anomalies 60 0.039
410
PRP030 Purpura 60 0.039
411
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.039
412
INT030 Intracranial Aneurysm 59 0.039
413
DBT062 Diabetic Foot Ulcers 58 0.039
414
HRT012 Heart Valve Disease 58 0.039
415
ZLL002 Zollinger-Ellison Syndrome 58 0.039
416
P ACT105 Acute Mountain Sickness 57 0.039
417
HLL004 Hellp Syndrome 57 0.039
418
PRS047 Prostatitis 56 0.039
419
MYM001 Myoma 56 0.039
420
BLD053 Blood Platelet Disease 56 0.039
421
c CHR320 Chiari Malformation Type I 55 0.039
422
HYP014 Hyperuricemia 55 0.039
423
P MCR010 Microcephaly 55 0.039
424
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 54 0.039
425
LMB062 Limb Ischemia 54 0.039
426
GNR004 Generalized Anxiety Disorder 54 0.039
427
P PRM006 Primary Biliary Cirrhosis 54 0.039
428
CRV040 Cervix Carcinoma 54 0.039
429
NPH091 Nephrolithiasis, Calcium Oxalate 54 0.039
430
STM007 Stomatitis 53 0.039
431
PRS129 Prostatic Hyperplasia, Benign 53 0.039
432
BLL003 Bell's Palsy 53 0.039
433
HMC014 Homocysteinemia 53 0.039
434
P END046 Endometritis 52 0.039
435
DNT012 Dental Caries 52 0.039
436
ADT003 Auditory System Disease 52 0.039
437
LRY017 Laryngeal Disease 51 0.039
438
P CHL066 Cholangitis 51 0.039
439
SPN021 Spinal Meningioma 50 0.039
440
P HYP073 Hypersensitivity Reaction Type Iv Disease 50 0.039
441
PTH003 Pathologic Nystagmus 50 0.039
442
P KRT007 Keratoconus 50 0.039
443
FCL012 Facial Paralysis 50 0.039
444
OCL069 Ocular Motor Apraxia 49 0.039
445
MLR006 Male Reproductive Organ Cancer 49 0.039
446
HYP017 Hypophosphatemia 49 0.039
447
CRV069 Cervix Disease 48 0.039
448
P CHN059 Chondrocalcinosis 48 0.039
449
MCR011 Microinvasive Gastric Cancer 47 0.039
450
P MYC033 Myoclonus 47 0.039
451
PRS042 Prostate Disease 47 0.039
452
FTL021 Fetal Macrosomia 46 0.039
453
PRM003 Premature Ejaculation 46 0.039
454
ATN004 Autonomic Neuropathy 46 0.039
455
CPL005 Capillary Disease 45 0.039
456
PPT001 Peptic Esophagitis 45 0.039
457
P HRD086 Hereditary Hypophosphatemic Rickets 45 0.039
458
ASP004 Asphyxia Neonatorum 44 0.039
459
RST023 Resting Heart Rate, Variation in 44 0.039
460
SLT001 Solitary Osseous Plasmacytoma 44 0.039
461
BLD054 Blood Protein Disease 43 0.039
462
c SRC023 Sarcoidosis 2 43 0.039
463
STT004 Steatorrhea 43 0.039
464
NVS015 Nevus Comedonicus 42 0.039
465
MTR007 Motor Peripheral Neuropathy 41 0.039
466
SCR001 Secretory Meningioma 41 0.039
467
c BLR024 Biliary Cirrhosis, Primary, 1 38 0.039
468
LYM002 Lymphoplasmacyte-Rich Meningioma 37 0.039
469
CRD220 Cardiac Valvular Defect, Developmental 36 0.039
470
CYT004 Cytomegalic Inclusion Disease 35 0.039
471
MYT011 Myotonia 34 0.039
473
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 33 0.039
474
PRS064 Persistent Vegetative State 33 0.039
475
P PRX010 Paroxysmal Ventricular Fibrillation 32 0.039
477
HPD002 Hepadnavirus Infection 24 0.039
478
VSL004 Visual Cortex Disease 23 0.039
479
MCR374 Microencephaly 22 0.039
480
MLT131 Multifocal Atrial Tachycardia 18 0.039
481
KRS005 Korsakoff's Amnesic Syndrome 16 0.039
482
P HPT023 Hepatocellular Carcinoma 96 0.032
483
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.032
484
CYS001 Cystic Fibrosis 82 0.032
485
INS024 Insulin-Like Growth Factor I 82 0.032
486
P DLT002 Dilated Cardiomyopathy 75 0.032
487
P MYS003 Myasthenia Gravis 73 0.032
488
WRN001 Werner Syndrome 73 0.032
489
c HPT073 Hepatitis C Virus 72 0.032
490
P RTN024 Retinoblastoma 72 0.032
491
ART016 Aortic Aneurysm 71 0.032
492
P BLD134 Bladder Cancer 70 0.032
493
MYL009 Myelodysplastic Syndrome 70 0.032
494
c HPT001 Hepatitis C 69 0.032
495
DRM006 Dermatitis 69 0.032
496
GRN037 Granulomatosis with Polyangiitis 69 0.032
497
ANR007 Anorexia Nervosa 68 0.032
498
P HYD006 Hydrocephalus 67 0.032
499
PNC033 Pancreas Adenocarcinoma 67 0.032
500
P HYP802 Hypocalcemia, Autosomal Dominant 1 66 0.032
501
P TXP001 Toxoplasmosis 66 0.032
502
P END044 Endometriosis 65 0.032
503
INT066 Interstitial Lung Disease 65 0.032
504
P AMY004 Amyloidosis 64 0.032
505
OST017 Osteomyelitis 64 0.032
506
INT002 Intermittent Claudication 64 0.032
507
P MSC007 Muscle Hypertrophy 64 0.032
508
P CND004 Candidiasis 63 0.032
509
P NPH012 Nephrotic Syndrome 63 0.032
510
LSC001 Lesch-Nyhan Syndrome 62 0.032
511
CRC021 Carcinosarcoma 62 0.032
512
WLF001 Wolff-Parkinson-White Syndrome 61 0.032
513
P LYM031 Lymphocytic Leukemia 61 0.032
514
P FBR017 Fibrosarcoma 61 0.032
515
P BPL003 Bipolar Disorder 61 0.032
516
c PRM005 Primary Hyperparathyroidism 60 0.032
517
P CTR002 Cataract 59 0.032
518
P PGT001 Paget's Disease of Bone 59 0.032
519
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 58 0.032
520
SQM006 Squamous Cell Carcinoma 58 0.032
521
P MTR012 Mitral Valve Disease 58 0.032
522
VSC002 Vascular Dementia 57 0.032
523
P TCD001 Tic Disorder 57 0.032
524
P PNC025 Panic Disorder 57 0.032
525
c CNG216 Congenital Hydrocephalus 57 0.032
526
MCN007 Meconium Aspiration Syndrome 57 0.032
527
P PLY019 Polyneuropathy 57 0.032
528
P HYP076 Hyperthyroidism 55 0.032
529
PRS021 Prostatic Adenoma 55 0.032
530
TBR011 Tuberculous Meningitis 55 0.032
531
P FBR031 Febrile Seizures 55 0.032
532
SPN051 Spondylitis 55 0.032
533
TST014 Testicular Cancer 54 0.032
534
GTR002 Goiter 54 0.032
535
P HMR005 Hemorrhoid 54 0.032
536
c PYR010 Peyronie's Disease 54 0.032
537
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.032
538
MYL020 Myelomeningocele 53 0.032
539
ORL005 Oral Candidiasis 53 0.032
540
LKC003 Leukocyte Disease 52 0.032
541
OBS082 Obstructive Nephropathy 52 0.032
542
CLS016 Clostridium Difficile Colitis 52 0.032
543
P RNV001 Renovascular Hypertension 52 0.032
544
P MTC133 Mitochondrial Myopathy 52 0.032
545
PLM017 Pulmonary Alveolar Microlithiasis 52 0.032
546
c OVR114 Ovarian Cancer 1 51 0.032
547
P OST028 Osteochondroma 51 0.032
548
HMG002 Hemoglobinuria 51 0.032
549
SPC010 Speech and Communication Disorders 51 0.032
550
P RNL007 Renal Tubular Acidosis 51 0.032
551
ACT088 Acute Insulin Response 50 0.032
552
PRT030 Parathyroid Gland Disease 50 0.032
553
MGC001 Megacolon 50 0.032
554
CHR074 Choriocarcinoma 49 0.032
555
P MGR001 Migraine Without Aura 48 0.032
556
BNN003 Bone Inflammation Disease 48 0.032
557
c HNT004 Huntington Disease-Like 2 47 0.032
558
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.032
559
EXS001 Exostosis 47 0.032
560
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.032
561
CRB090 Cerebral Hypoxia 47 0.032
562
PRN009 Paranoid Schizophrenia 47 0.032
563
BRN041 Bornholm Eye Disease 45 0.032
564
PST053 Postherpetic Neuralgia 45 0.032
565
P CLS010 Cluster Headache 45 0.032
566
P MJR007 Major Affective Disorder 1 45 0.032
567
INT071 Intestinal Perforation 45 0.032
568
c GLL024 Gallbladder Disease 1 45 0.032
569
DYS015 Dysentery 45 0.032
570
P RNL045 Renal Tubular Acidosis, Distal 45 0.032
571
CRT015 Carotid Artery Occlusion 44 0.032
572
PLS016 Plasma Cell Leukemia 43 0.032
573
GST030 Gastrinoma 43 0.032
574
P TRC087 Tricuspid Valve Disease 43 0.032
575
GRD001 Giardiasis 42 0.032
576
SNL007 Senile Cataract 40 0.032
577
c PRS136 Prostate Cancer, Hereditary, 6 40 0.032
578
c PGT007 Paget Disease of Bone 3 39 0.032
579
c PLM022 Pulmonary Valve Insufficiency 39 0.032
580
PSD088 Pseudobulbar Affect 39 0.032
581
ART035 Arterial Calcification of Infancy 38 0.032
582
HRN029 Hearing Loss, Noise-Induced 38 0.032
583
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 37 0.032
584
UTR020 Uterine Inversion 37 0.032
585
c PRS130 Prostate Cancer, Hereditary, 8 37 0.032
586
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 36 0.032
587
c MYS011 Myasthenia Gravis Congenital 33 0.032
588
PRM050 Primary Orthostatic Tremor 33 0.032
589
PYR016 Pyridoxine Deficiency 33 0.032
590
BLD164 Blood Group, Gerbich System 31 0.032
591
CHR028 Chronic Wasting Disease 29 0.032
592
CHR158 Charles Bonnet Syndrome 26 0.032
593
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 26 0.032
594
MTR030 Mitral Valve Prolapse, Familial, X-Linked 25 0.032
595
IND003 Indolent Myeloma 24 0.032
596
PLS003 Plasmacytic Leukemia 24 0.032
597
HYP786 Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy 12 0.032
598
P LNG032 Lung Cancer 99 0.023
599
c SYS001 Systemic Lupus Erythematosus 88 0.023
600
P ATX030 Ataxia-Telangiectasia 82 0.023
601
P RHM011 Rheumatoid Arthritis 81 0.023
602
CRH001 Crohn's Disease 79 0.023
603
NRL016 Neural Tube Defects 79 0.023
604
P PRK057 Parkinson Disease, Late-Onset 76 0.023
605
HMN044 Human Immunodeficiency Virus Type 1 75 0.023
606
MRF001 Marfan Syndrome 75 0.023
607
PLM001 Pulmonary Tuberculosis 74 0.023
608
PHN003 Phenylketonuria 74 0.023
609
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 72 0.023
610
P BDY004 Body Mass Index Quantitative Trait Locus 11 72 0.023
611
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.023
612
P DRM053 Dermatitis, Atopic 71 0.023
613
c PLM164 Pulmonary Hypertension, Primary, 1 70 0.023
614
CNN003 Conn's Syndrome 70 0.023
615
SRC014 Sarcoma 70 0.023
616
LYM017 Lyme Disease 70 0.023
617
P PLM036 Pulmonary Fibrosis 70 0.023
618
c ATR087 Atrial Standstill 1 70 0.023
619
P LPS004 Lupus Erythematosus 69 0.023
620
LSH001 Leishmaniasis 69 0.023
621
P LKM062 Leukemia, Acute Lymphoblastic 68 0.023
622
c SML038 Small Cell Cancer of the Lung 68 0.023
623
OBS002 Obsessive-Compulsive Disorder 68 0.023
624
ATM095 Autoimmune Disease 68 0.023
625
ACH004 Achondroplasia 68 0.023
626
CHR066 Chronic Fatigue Syndrome 68 0.023
627
P SYS005 Systemic Scleroderma 67 0.023
628
c SCL052 Scleroderma, Familial Progressive 67 0.023
629
P MYC084 Mycobacterium Tuberculosis 1 67 0.023
630
P HYP098 Hypereosinophilic Syndrome 67 0.023
631
c ATM011 Autoimmune Hepatitis 67 0.023
632
GLL008 Gilles De La Tourette Syndrome 67 0.023
633
OST003 Osteonecrosis 67 0.023
634
MVM001 Movement Disease 67 0.023
635
c ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.023
636
PRD007 Periodontal Disease 66 0.023
637
c MCR129 Microvascular Complications of Diabetes 1 66 0.023
638
P ENC004 Encephalitis 66 0.023
639
P ALP009 Alopecia Areata 66 0.023
640
GST040 Gastric Adenocarcinoma 66 0.023
641
P DYS154 Dystonia 65 0.023
642
P CNJ013 Conjunctivitis 65 0.023
643
c NNN010 Noonan Syndrome 3 65 0.023
644
ETN001 Eating Disorder 65 0.023
645
c LCL006 Localized Scleroderma 65 0.023
646
P DRM010 Dermatomyositis 65 0.023
647
MSL001 Measles 65 0.023
648
P ANR048 Aniridia 1 64 0.023
649
ACN002 Acanthosis Nigricans 64 0.023
650
P ANG001 Angelman Syndrome 64 0.023
651
PRT010 Parathyroid Carcinoma 64 0.023
652
INS001 Insulinoma 64 0.023
653
FLL027 Fallopian Tube Carcinoma 64 0.023
654
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.023
655
GNG013 Gingivitis 63 0.023
656
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 63 0.023
657
IMM167 Immune Deficiency Disease 63 0.023
658
P TST021 Testicular Germ Cell Tumor 63 0.023
659
PST028 Post-Traumatic Stress Disorder 63 0.023
660
P MCH002 Machado-Joseph Disease 63 0.023
661
P THY023 Thymoma 63 0.023
662
P PLV020 Pelvic Organ Prolapse 62 0.023
663
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.023
664
KRT001 Keratoconjunctivitis Sicca 62 0.023
665
c PNC108 Pancreatitis, Hereditary 62 0.023
666
c ACT073 Acute Leukemia 62 0.023
667
P GLL020 Gallbladder Disease 62 0.023
668
LPT001 Leptospirosis 62 0.023
669
P GLY013 Glycogen Storage Disease 61 0.023
670
P NMN002 Niemann-Pick Disease 61 0.023
671
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 61 0.023
672
PLL001 Pallister-Hall Syndrome 61 0.023
673
AND002 Androgen Insensitivity Syndrome 61 0.023
674
CHR103 Charge Syndrome 61 0.023
675
P CMR001 Camurati-Engelmann Disease 61 0.023
676
P HMN010 Hemangioma 61 0.023
677
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.023
678
VSC003 Visceral Leishmaniasis 61 0.023
679
P HRD008 Hereditary Hemorrhagic Telangiectasia 60 0.023
680
JPN002 Japanese Encephalitis 60 0.023
681
P SML001 Small Cell Carcinoma 60 0.023
682
CHL014 Cholera 60 0.023
683
P LTR001 Lateral Sclerosis 60 0.023
684
ORP003 Oropharynx Cancer 60 0.023
685
MTR014 Motor Neuron Disease 60 0.023
686
AVN001 Avian Influenza 60 0.023
687
c VRL010 Viral Hepatitis 60 0.023
688
DMY004 Demyelinating Disease 60 0.023
689
DBT010 Diabetic Neuropathy 60 0.023
690
EMB004 Embryonal Carcinoma 59 0.023
691
WST001 West Syndrome 59 0.023
692
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 59 0.023
693
c PRD040 Periodontitis, Chronic 59 0.023
694
TRN015 Transient Cerebral Ischemia 59 0.023
695
ART001 Arterial Tortuosity Syndrome 59 0.023
696
P MYP006 Myopia 59 0.023
697
c ACT027 Acute Pancreatitis 59 0.023
698
P KDN017 Kidney Cancer 59 0.023
699
CHL028 Childhood Type Dermatomyositis 59 0.023
700
PRM126 Primary Peritoneal Carcinoma 59 0.023
701
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 58 0.023
702
c MYT020 Myotonic Dystrophy 2 58 0.023
703
EXT034 Extrinsic Allergic Alveolitis 58 0.023
704
c BLD124 Bleeding Disorder, Platelet-Type, 11 58 0.023
705
P PLY041 Polymyositis 58 0.023
706
P AXN002 Axenfeld-Rieger Syndrome 57 0.023
707
LYM027 Lymphopenia 57 0.023
708
ERY029 Erythermalgia, Primary 57 0.023
709
ICH054 Ichthyosis, X-Linked 57 0.023
710
HDR002 Hidradenitis Suppurativa 57 0.023
711
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.023
712
c GRV008 Graves Disease 1 57 0.023
713
MVL001 Mevalonic Aciduria 57 0.023
714
PLR022 Pleural Disease 56 0.023
715
IMP005 Impotence 56 0.023
716
c ACT068 Acute Cystitis 56 0.023
717
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.023
718
P RTN016 Retinal Degeneration 56 0.023
719
MMM001 Mammary Paget's Disease 56 0.023
720
THR013 Thoracic Outlet Syndrome 56 0.023
721
NTR046 Neutrophil Migration 56 0.023
722
P ALP008 Alopecia 56 0.023
723
TLN003 Telangiectasis 56 0.023
724
LNG031 Lung Benign Neoplasm 56 0.023
725
TCK001 Tick-Borne Encephalitis 56 0.023
726
P MSC003 Muscular Atrophy 56 0.023
727
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.023
728
IRN001 Iron Deficiency Anemia 55 0.023
729
FRS002 Frasier Syndrome 55 0.023
730
P DBT005 Diabetes Insipidus 55 0.023
731
GLL018 Gallbladder Cancer 55 0.023
732
THR004 Thrombocytosis 55 0.023
733
P CRN108 Cranioectodermal Dysplasia 1 55 0.023
734
SCH012 Schizoaffective Disorder 54 0.023
735
SPN041 Spinal Cord Disease 54 0.023
736
P MGR003 Migraine with Aura 54 0.023
737
P PTT006 Pituitary Adenoma 54 0.023
738
ATR057 Atrioventricular Block 54 0.023
739
P INT099 Intrahepatic Cholestasis of Pregnancy 53 0.023
740
GRM005 Germ Cell Cancer 53 0.023
741
P OBS001 Obstructive Jaundice 53 0.023
742
FRZ001 Frozen Shoulder 53 0.023
743
AML029 Ameloblastoma 53 0.023
744
CHR100 Chronic Ulcer of Skin 53 0.023
745
OLG003 Oligohydramnios 53 0.023
746
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 53 0.023
747
BSC001 Buschke-Ollendorff Syndrome 53 0.023
748
ALL009 Allergic Conjunctivitis 53 0.023
749
HPR003 Heparin-Induced Thrombocytopenia 53 0.023
750
c ALP106 Alport Syndrome 1, X-Linked 53 0.023
751
DRY001 Dry Eye Syndrome 53 0.023
752
ALC009 Alcoholic Liver Cirrhosis 52 0.023
753
INT067 Interstitial Nephritis 52 0.023
754
P MLN007 Male Infertility 52 0.023
755
c ART120 Arthrogryposis, Distal, Type 3 52 0.023
756
P TRT010 Teratoma 52 0.023
757
TST015 Testicular Disease 52 0.023
758
c CHR418 Chronic Leukemia 52 0.023
759
CYC008 Cyclic Vomiting Syndrome 52 0.023
760
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.023
761
PRT029 Parathyroid Adenoma 52 0.023
762
OST011 Osteomalacia 52 0.023
763
NSD001 Nose Disease 52 0.023
764
RYN005 Raynaud Phenomenon 52 0.023
765
HDR003 Hidradenitis 52 0.023
766
c RTN162 Retinitis Pigmentosa 2 51 0.023
767
MTN003 Motion Sickness 51 0.023
768
NRG002 Neurogenic Bladder 51 0.023
769
END021 Endomyocardial Fibrosis 51 0.023
770
PRD004 Prediabetes Syndrome 51 0.023
771
BRX001 Bruxism 51 0.023
772
CCN002 Cocaine Abuse 51 0.023
773
c FML023 Familial Hemiplegic Migraine 50 0.023
774
CRN019 Coronary Artery Vasospasm 50 0.023
775
HRP009 Herpes Simplex Encephalitis 50 0.023
776
c THY107 Thymoma, Familial 50 0.023
777
P NGH001 Night Blindness 50 0.023
778
DBT004 Diabetic Polyneuropathy 50 0.023
779
NWC001 Newcastle Disease 50 0.023
780
HYP043 Hyperandrogenism 50 0.023
781
HYP781 Hypoascorbemia 50 0.023
782
ESN002 Eosinophilia-Myalgia Syndrome 50 0.023
783
HPT082 Hepatic Adenomas, Familial 50 0.023
784
c MLG069 Malignant Hypertension 50 0.023
785
P HMP006 Hemiplegic Migraine 49 0.023
786
SCL003 Social Phobia 49 0.023
787
MLT006 Multidrug-Resistant Tuberculosis 49 0.023
788
ZKF001 Zika Fever 49 0.023
789
P MYT023 Myotonia Congenita 49 0.023
790
CRB016 Carbuncle 49 0.023
791
URT010 Ureteral Obstruction 49 0.023
792
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.023
793
VTM002 Vitamin B12 Deficiency 48 0.023
794
CLN045 Colonic Benign Neoplasm 48 0.023
795
DBT008 Diabetic Angiopathy 48 0.023
796
BSL008 Basal Ganglia Disease 48 0.023
797
P ART084 Arteriovenous Fistula 48 0.023
798
CNT025 Central Pontine Myelinolysis 48 0.023
799
ORL015 Oral Squamous Cell Carcinoma 48 0.023
800
P ERY008 Erythromelalgia 48 0.023
801
NRT001 Neurotic Disorder 47 0.023
802
NRR001 Neuroretinitis 47 0.023
803
RTN001 Retinal Vasculitis 47 0.023
804
P GNT008 Giant Cell Tumor 47 0.023
805
ANC002 Anca-Associated Vasculitis 47 0.023
806
DWR001 Dwarfism 47 0.023
807
PRT035 Peritoneum Cancer 47 0.023
808
EVN001 Evans' Syndrome 47 0.023
809
ATN013 Autoinflammation, Panniculitis, and Dermatosis Syndrome 47 0.023
810
P LYD001 Leydig Cell Tumor 47 0.023
811
BLR013 Biliary Tract Cancer 47 0.023
812
MYC005 Myocardial Stunning 47 0.023
813
GLC096 Galactorrhea 47 0.023
814
MTC005 Mitochondrial Metabolism Disease 47 0.023
815
c ACT076 Acute Myocarditis 47 0.023
816
UPP004 Upper Respiratory Tract Disease 47 0.023
817
P END039 Endodermal Sinus Tumor 47 0.023
818
PMP004 Pemphigus Foliaceus 46 0.023
819
TCL003 T Cell Deficiency 46 0.023
820
DBT002 Diabetic Autonomic Neuropathy 46 0.023
821
SMN007 Seminoma 46 0.023
822
DFF003 Diffuse Scleroderma 46 0.023
823
RFR003 Refractive Error 46 0.023
824
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 46 0.023
825
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.023
826
ISC015 Ischemic Colitis 46 0.023
827
P DNR001 Duane Retraction Syndrome 46 0.023
828
AGR002 Agoraphobia 45 0.023
829
SDD008 Sudden Sensorineural Hearing Loss 45 0.023
830
c CRN243 Carney Complex, Type 1 45 0.023
831
c HYP794 Hyperoxaluria, Primary, Type I 45 0.023
832
c SHR030 Short Qt Syndrome 44 0.023
833
c BDY020 Body Mass Index Quantitative Trait Locus 19 44 0.023
834
P TST026 Testicular Germ Cell Cancer 44 0.023
835
TST018 Testicular Yolk Sac Tumor 44 0.023
836
STP004 Staphylococcal Toxic Shock Syndrome 44 0.023
837
CNN001 Cannabis Dependence 44 0.023
838
ENT004 Enthesopathy 44 0.023
839
TRC023 Trichinosis 44 0.023
840
BRS064 Bursitis 44 0.023
841
ACT003 Acute Kidney Tubular Necrosis 44 0.023
842
PHT003 Phototoxic Dermatitis 44 0.023
843
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 44 0.023
844
c BRT042 Bartter Syndrome, Type 3 44 0.023
845
INT052 Intestinal Volvulus 43 0.023
846
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 43 0.023
847
PLY024 Polymicrogyria 43 0.023
848
ALL014 Allergic Encephalomyelitis 43 0.023
849
PHB001 Phobic Disorder 43 0.023
850
c HYP057 Hypervitaminosis D 43 0.023
851
HYP706 Hypermobile Ehlers-Danlos Syndrome 43 0.023
852
c BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.023
853
MYC017 Mycobacterium Kansasii 43 0.023
854
ADP007 Adie Pupil 42 0.023
855
CRD137 Cardiogenic Shock 42 0.023
856
P FML187 Familial Hypertension 42 0.023
857
c MCR112 Microvascular Complications of Diabetes 2 42 0.023
858
CNN002 Cannabis Abuse 42 0.023
859
OVR112 Ovarian Germ Cell Cancer 42 0.023
860
ETH004 Euthyroid Sick Syndrome 42 0.023
861
THR099 Third-Degree Atrioventricular Block 42 0.023
862
MCR018 Microcytic Anemia 42 0.023
863
MTS001 Mutism 42 0.023
864
c BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.023
865
c BDY006 Body Mass Index Quantitative Trait Locus 8 41 0.023
866
c BDY012 Body Mass Index Quantitative Trait Locus 7 41 0.023
867
AMN006 Aminoaciduria 41 0.023
868
c BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.023
869
FRN014 Fournier Gangrene 41 0.023
870
EXC002 Exocrine Pancreatic Insufficiency 41 0.023
871
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 40 0.023
872
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 40 0.023
873
PRN039 Paraneoplastic Syndromes 40 0.023
874
c DNR003 Duane Retraction Syndrome 1 40 0.023
875
ALR002 Al-Raqad Syndrome 40 0.023
876
TST043 Testicular Seminoma 40 0.023
877
SPR024 Supratentorial Cancer 40 0.023
878
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.023
879
HLX001 Helix Syndrome 40 0.023
880
c MJR023 Major Affective Disorder 7 39 0.023
881
ATX010 Ataxia Neuropathy Spectrum 39 0.023
882
RTR001 Retrograde Amnesia 39 0.023
883
CHR076 Choriocarcinoma of the Testis 39 0.023
884
BRK012 Broken Heart Syndrome 39 0.023
885
BCK003 Background Diabetic Retinopathy 38 0.023
886
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.023
887
c TST017 Testicular Malignant Germ Cell Cancer 38 0.023
888
FRS012 First-Degree Atrioventricular Block 38 0.023
889
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 38 0.023
890
FCL044 Fecal Incontinence 38 0.023
891
TNS007 Taeniasis 38 0.023
892
OBS004 Obstructive Hydrocephalus 37 0.023
893
P HYP733 Hypercalciuria, Absorptive, 2 37 0.023
894
EMB006 Embryonal Testis Carcinoma 36 0.023
895
EXT001 Extragonadal Seminoma 36 0.023
896
c MJR022 Major Affective Disorder 8 36 0.023
897
c MJR024 Major Affective Disorder 9 36 0.023
898
P CNT036 Central Nervous System Germ Cell Tumor 36 0.023
899
HYP034 Hypertensive Encephalopathy 36 0.023
900
FRS019 Farsightedness 36 0.023
901
c PLM127 Pulmonary Hypertension, Primary, 3 35 0.023
902
GRM010 Germ Cells Tumors 35 0.023
903
EXT025 Extragonadal Germ Cell Cancer 35 0.023
904
PCD001 Pica Disease 35 0.023
905
c TST046 Testicular Germ Cell Tumor 1 35 0.023
906
FLL029 Fallopian Tube Disease 35 0.023
907
TST020 Testis Seminoma 34 0.023
908
NNS011 Nonseminomatous Germ Cell Tumor 34 0.023
909
MXD025 Mixed Germ Cell Cancer 34 0.023
910
MXD032 Mixed Germ Cell Tumor 34 0.023
911
SVR002 Severe Nonproliferative Diabetic Retinopathy 34 0.023
912
URN022 Urinary Tract Infections, Recurrent 34 0.023
913
MYC088 Mycobacterium Avium Complex Infections 33 0.023
914
PPL052 Papillomatosis, Confluent and Reticulated 33 0.023
915
PDP001 Pedophilia 33 0.023
916
c KNN009 Kenny-Caffey Syndrome, Type 1 33 0.023
917
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 33 0.023
918
PRP015 Paraphilia Disorder 32 0.023
919
NTR027 Neutrophil Actin Dysfunction 32 0.023
920
GST007 Gastric Dilatation 32 0.023
921
HNM002 Hinman Syndrome 31 0.023
922
NRL001 Neurilemmoma of the Fifth Cranial Nerve 31 0.023
923
SPN125 Spondyloenchondrodysplasia 31 0.023
924
SLL001 Sialolithiasis 30 0.023
925
P ACT232 Acute Necrotizing Encephalopathy 30 0.023
926
PRX008 Paroxysmal Cold Hemoglobinuria 30 0.023
927
RVR002 Reversible Cerebral Vasoconstriction Syndrome 29 0.023
928
P STR035 Streptococcal Group a Invasive Disease 29 0.023
929
AKN002 Akinetic Mutism 29 0.023
930
BLD163 Blood Group, Dombrock System 27 0.023
931
BLD151 Blood Group--Wright Antigen 26 0.023
932
OVR015 Ovarian Mixed Germ Cell Neoplasm 26 0.023
933
HDC005 Headache Associated with Sexual Activity 26 0.023
934
TLG001 Telogen Effluvium 26 0.023
935
c ADL057 Adult Teratoma 25 0.023
936
OVR077 Overuse Syndrome 25 0.023
937
CML001 Cumulative Trauma Disorders 25 0.023
938
BLD137 Blood Group--Ahonen 24 0.023
939
RPT005 Repetitive Motion Disorders 24 0.023
940
c CHR464 Chronic Intestinal Failure 24 0.023
941
OSM001 Osmotic Diarrhea 24 0.023
942
EXT053 Extragonadal Nonseminomatous Germ Cell Tumor 23 0.023
943
LRB003 Lrba Deficiency 23 0.023
944
CHR189 Chromosome 12p Deletion 23 0.023
945
ORP004 Oropharyngeal Cancer, Adult 22 0.023
946
PRQ002 Paraquat Poisoning 22 0.023
947
PLM069 Pulmonary Venous Return Anomaly 22 0.023
948
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 21 0.023
949
AND005 Androgen Insensitivity Syndrome, Mild 21 0.023
950
URM001 Uremic Neuropathy 21 0.023
951
c RTN181 Retinitis Pigmentosa 2, X-Linked 21 0.023
952
MSL005 Mseleni Joint Disease 20 0.023
953
EPL050 Epilepsy, Partial, with Pericentral Spikes 20 0.023
954
CRN167 Caronte 19 0.023
955
RTN199 Retinal Venous Beading 18 0.023
956
FBR065 Fibrocalculous Pancreatopathy 18 0.023
957
STP007 Staphylococcal Scarlet Fever 18 0.023
958
c HYP302 Hypomagnesemia 4, Renal 17 0.023
959
c CNT032 Central Nervous System Adult Germ Cell Tumor 17 0.023
960
RPT006 Repetitive Stress Injuries 16 0.023
961
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 13 0.023
962
HND012 Handigodu Joint Disease 13 0.023
963
DGT004 Digitalis Poisoning 12 0.023
964
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 10 0.023
965
HND010 Handigodu Disease 10 0.023
966
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 5 0.023
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