Search results for Magnesium

991 hits were found for Magnesium

# Family MCID Name MIFTS Score
1
IMM110 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection and Neoplasia 24 7.291
2
c HYP210 Hypomagnesemia 2, Renal 33 6.143
3
HYP550 Hypomagnesemia 1, Intestinal 39 4.103
4
XLN022 X-Linked Magnesium Deficiency with Epstein-Barr Virus Infection and Neoplasia 9 4.032
5
GTL001 Gitelman Syndrome 61 3.332
6
P HYP534 Hypomagnesemia 3, Renal 29 2.409
7
P ECL001 Eclampsia 54 0.179
8
c PRC016 Pre-Eclampsia 56 0.157
9
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.141
10
P AST005 Asthma 82 0.126
11
PRP027 Peripheral Vascular Disease 68 0.126
12
PLC008 Placenta Disease 33 0.126
13
c SVR005 Severe Pre-Eclampsia 49 0.124
14
c PND001 Pain Disorder 54 0.118
15
NPH003 Nephrocalcinosis 48 0.114
16
P NRV006 Nervous System Cancer 60 0.111
17
PRP021 Peripheral Nervous System Neoplasm 46 0.111
18
PRM237 Primary Hypomagnesemia 42 0.111
19
P ENC018 Encephalopathy 59 0.109
20
SNS023 Sensory System Cancer 43 0.109
21
NTR005 Nutritional Deficiency Disease 36 0.109
22
P PRC031 Preeclampsia/eclampsia 1 51 0.107
23
CRB009 Cerebritis 39 0.107
24
ISC004 Ischemia 61 0.102
25
NRM005 Neuromuscular Disease 56 0.097
26
BRN038 Bronchial Disease 51 0.097
27
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.097
28
P HRT032 Heart Disease 75 0.094
29
ATP002 Atopy 66 0.094
30
GST092 Gastroesophageal Reflux 62 0.094
31
P MYP004 Myopathy 67 0.092
32
LNG099 Lung Disease 64 0.092
33
MTH009 Mouth Disease 61 0.092
34
RSP006 Respiratory System Disease 58 0.092
35
P SZR006 Seizure Disorder 56 0.092
36
IMP003 Impaired Renal Function Disease 34 0.092
37
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.089
38
PRP019 Peripheral Nervous System Disease 55 0.089
39
P MSC033 Muscle Disorders 52 0.089
40
PRP080 Peripheral Artery Disease 37 0.089
41
c AST039 Asthma 2 28 0.089
42
P OBS005 Obesity 92 0.086
43
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.086
44
URN009 Urinary System Disease 50 0.086
45
CSY001 C Syndrome 50 0.086
46
P URF003 Urofacial Syndrome 1 50 0.086
47
MSC004 Muscle Tissue Disease 34 0.086
48
c CRN175 Coronary Heart Disease 4 19 0.086
49
c CHR089 Chronic Kidney Failure 66 0.083
50
APH001 Aphthous Stomatitis 62 0.083
51
GST050 Gastrointestinal System Disease 56 0.083
52
BRN071 Brain Injury 52 0.083
53
HYP005 Hypokalemia 51 0.083
54
END072 Endotheliitis 42 0.083
55
GST078 Gastrointestinal Allergy 40 0.083
56
c HYP595 Hypertension, Essential 69 0.080
57
CRB039 Cerebrovascular Disease 63 0.080
58
P GST049 Gastrointestinal System Cancer 60 0.080
59
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.080
60
HYP025 Hyperphosphatemia 47 0.080
61
STT002 Status Asthmaticus 42 0.080
62
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.080
63
P MYC007 Myocardial Infarction 79 0.077
64
VSC007 Vascular Disease 67 0.077
65
CRB037 Cerebral Palsy 66 0.077
66
P KDN018 Kidney Disease 66 0.077
67
HMT002 Hematologic Cancer 64 0.077
68
WLL006 Wells Syndrome 59 0.077
69
LPD008 Lipid Metabolism Disorder 58 0.077
70
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.077
71
CLC006 Calcinosis 50 0.077
72
INT253 Intestinal Benign Neoplasm 47 0.077
73
CRB085 Cerebral Hemorrhage 46 0.077
74
BLD053 Blood Platelet Disease 46 0.077
75
GDS001 Good Syndrome 44 0.077
76
GLC008 Glucose Metabolism Disease 42 0.077
77
c PRC034 Preeclampsia/eclampsia 4 23 0.077
78
P CLR023 Colorectal Cancer 97 0.074
79
ATH003 Atherosclerosis 65 0.074
80
DFC004 Deficiency Anemia 64 0.074
81
c CNT035 Central Nervous System Disease 60 0.074
82
ADN018 Adenoma 58 0.074
83
ESP023 Esophageal Disease 54 0.074
84
CLN019 Colonic Disease 51 0.074
85
P CHR345 Chronic Pain 50 0.074
86
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.074
87
P BLD051 Blood Coagulation Disease 42 0.074
88
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.074
89
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.074
90
MNR003 Mineral Metabolism Disease 38 0.074
91
BNS002 Bone Structure Disease 37 0.074
92
VSC008 Vascular Hemostatic Disease 30 0.074
93
c AST037 Asthma 1 28 0.074
94
ADG002 Audiogenic Seizures 24 0.074
95
c CRN214 Coronary Heart Disease 5 22 0.074
96
c PRC033 Preeclampsia/eclampsia 3 16 0.074
97
P LVR013 Liver Disease 75 0.070
98
STR067 Stroke, Ischemic 75 0.070
99
P CRN211 Coronary Artery Disease 74 0.070
100
P NRV007 Nervous System Disease 71 0.070
101
ISC006 Ischemic Heart Disease 68 0.070
102
P ESP024 Esophagitis 61 0.070
103
c ACT075 Acute Myocardial Infarction 60 0.070
104
P DRR001 Diarrhea 60 0.070
105
ART111 Artery Disease 55 0.070
106
END030 End Stage Renal Failure 55 0.070
107
RCT018 Rectal Neoplasm 54 0.070
108
P SPS003 Spastic Diplegia 52 0.070
109
ATR060 Atrial Standstill, Digenic 51 0.070
110
DYS073 Dysphagia 48 0.070
111
FML039 Female Reproductive System Disease 48 0.070
112
PRT030 Parathyroid Gland Disease 47 0.070
113
BRD001 Brody Myopathy 47 0.070
114
CRB025 Carbohydrate Metabolic Disorder 46 0.070
115
CCN007 Cocoon Syndrome 45 0.070
116
BRT030 Birth Defects 43 0.070
117
BHR001 Behr Syndrome 42 0.070
118
RCT017 Rectal Disease 40 0.070
119
SPN369 Spinal Disease 39 0.070
120
c ART106 Arterial Calcification, Generalized, of Infancy, 1 39 0.070
121
SWL001 Swallowing Disorders 33 0.070
122
SCR035 Sacral Agenesis with Vertebral Anomalies 30 0.070
123
P LKM002 Leukemia 71 0.067
124
P HML002 Hemolytic Anemia 62 0.067
125
ART021 Arteriosclerosis 58 0.067
126
P HYP060 Hyperinsulinism 58 0.067
127
HYP266 Hypoxia 56 0.067
128
VRL011 Viral Infectious Disease 55 0.067
129
ADL002 Adult Syndrome 52 0.067
130
BRN004 Brain Edema 52 0.067
131
SCK005 Sickle Cell Disease 51 0.067
132
STM006 Stomach Disease 50 0.067
133
CRB004 Cerebral Artery Occlusion 45 0.067
134
c CLR079 Colorectal Cancer 2 29 0.067
135
PRM243 Primary Bone Cancer 29 0.067
136
GST038 Gastrointestinal Adenoma 27 0.067
137
c PRC032 Preeclampsia/eclampsia 2 16 0.067
138
MXD001 Mixed Cerebral Palsy 16 0.067
139
CNG034 Congestive Heart Failure 72 0.063
140
SCK003 Sickle Cell Anemia 71 0.063
141
P ATR011 Atrial Fibrillation 66 0.063
142
P NRP001 Neuropathy 59 0.063
143
CHL071 Child Syndrome 58 0.063
144
GST023 Gastric Ulcer 56 0.063
145
KDS001 Kid Syndrome 53 0.063
146
P HYP024 Hypoparathyroidism 53 0.063
147
HMG005 Hemoglobinopathy 52 0.063
148
ALL026 Allergic Hypersensitivity Disease 52 0.063
149
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.063
150
c CNG027 Congenital Hemolytic Anemia 48 0.063
151
ACR041 Acromelic Frontonasal Dysostosis 45 0.063
152
CLN044 Colon Adenoma 44 0.063
153
SKN023 Skin Tag 44 0.063
154
PRD011 Proud Syndrome 42 0.063
155
BRN080 Brain Ischemia 41 0.063
156
ALR002 Al-Raqad Syndrome 36 0.063
157
DYS011 Dyskinesia of Esophagus 28 0.063
158
c HYP445 Hypomagnesemia 6, Renal 25 0.063
159
P INT068 Intestinal Disease 60 0.059
160
P ORL007 Oral Cavity Cancer 59 0.059
161
c FML001 Familial Atrial Fibrillation 58 0.059
162
CNS004 Constipation 57 0.059
163
EXF001 Exfoliation Syndrome 57 0.059
164
ORL011 Oral Cancer 56 0.059
165
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.059
166
SLP005 Sleep Disorder 53 0.059
167
TXC002 Toxic Encephalopathy 51 0.059
168
HRT007 Heart Cancer 46 0.059
169
INC022 Inclusion-Cell Disease 46 0.059
170
SNS003 Sensory Peripheral Neuropathy 45 0.059
171
P PLN008 Peeling Skin Syndrome 45 0.059
172
HDN002 Head Injury 45 0.059
173
ALN001 Aland Island Eye Disease 45 0.059
174
ACT058 Active Peptic Ulcer Disease 43 0.059
175
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.059
176
ATN003 Autonomic Nervous System Neoplasm 40 0.059
177
P HRT017 Heart Tumor 32 0.059
178
c CLR075 Colorectal Cancer 3 28 0.059
179
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.059
180
SBC016 Subacute Delirium 24 0.059
181
P CRN178 Coronary Heart Disease 6 21 0.059
182
c CRN172 Coronary Heart Disease 3 19 0.059
183
c CRN173 Coronary Heart Disease 8 18 0.059
184
c ADL079 Adult Heart Tumor 16 0.059
185
P HNT016 Huntington Disease 80 0.055
186
P ADN016 Adenocarcinoma 69 0.055
187
SKN016 Skin Disease 66 0.055
188
P EPL164 Epilepsy 66 0.055
189
P OST002 Osteoporosis 64 0.055
190
P RCK004 Rickets 61 0.055
191
MDD011 Mood Disorder 61 0.055
192
PRM097 Primary Immunodeficiency Disease 60 0.055
193
OCL009 Ocular Cancer 59 0.055
194
BNC003 Bone Cancer 58 0.055
195
KND001 Kindler Syndrome 57 0.055
196
THR024 Thrombosis 57 0.055
197
P HMR003 Hemorrhagic Disease 57 0.055
198
PLY023 Polycystic Liver Disease 56 0.055
199
P MCR129 Microvascular Complications of Diabetes 1 54 0.055
200
P SML016 Small Intestine Cancer 52 0.055
201
BRN106 Burns 52 0.055
202
KRT002 Keratomalacia 52 0.055
203
PRT011 Protein C Deficiency 52 0.055
204
MVM001 Movement Disease 49 0.055
205
c ACT071 Acute Kidney Failure 49 0.055
206
c CLR085 Colorectal Cancer 1 45 0.055
207
VSC047 Vascular Malformation 45 0.055
208
RNL011 Renal Osteodystrophy 45 0.055
209
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.055
210
RPR002 Reproductive System Disease 41 0.055
211
c PLN018 Peeling Skin Syndrome 2 40 0.055
212
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.055
213
BLD054 Blood Protein Disease 37 0.055
214
c PLN021 Peeling Skin Syndrome 3 29 0.055
215
c TRC078 Trichohepatoenteric Syndrome 2 29 0.055
216
CRB031 Cerebral Arterial Disease 27 0.055
217
ACT174 Acute Peripheral Arterial Occlusion 15 0.055
218
P HPT023 Hepatocellular Carcinoma 92 0.050
219
P INF038 Influenza 72 0.050
220
P RSP003 Respiratory Failure 71 0.050
221
ANX002 Anxiety Disorder 67 0.050
222
LVR012 Liver Cirrhosis 67 0.050
223
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.050
224
DMN002 Dementia 65 0.050
225
P HYP086 Hypothyroidism 64 0.050
226
ALC007 Alcohol Dependence 63 0.050
227
BRS051 Breast Disease 61 0.050
228
TTN003 Tetanus 61 0.050
229
P SHR029 Short Syndrome 58 0.050
230
ART017 Aortic Disease 57 0.050
231
GST033 Gestational Diabetes 57 0.050
232
ANR040 Aneurysm 57 0.050
233
WST001 West Syndrome 57 0.050
234
P HYP192 Hypocalcemia, Autosomal Dominant 56 0.050
235
PHR003 Pharyngitis 56 0.050
236
END040 Endogenous Depression 53 0.050
237
MNT002 Mental Depression 53 0.050
238
VSC006 Vascular Cancer 51 0.050
239
GNR004 Generalized Anxiety Disorder 51 0.050
240
INT007 Intermediate Coronary Syndrome 50 0.050
241
P DDN001 Duodenal Ulcer 50 0.050
242
BNF002 Bone Fracture 50 0.050
243
P CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 48 0.050
244
ATN002 Autonomic Nervous System Disease 48 0.050
245
PRV004 Periventricular Leukomalacia 48 0.050
246
c HMG001 Hemoglobin C Disease 47 0.050
247
PLC007 Placental Abruption 47 0.050
248
CRB090 Cerebral Hypoxia 45 0.050
249
BWN001 Bowen-Conradi Syndrome 44 0.050
250
SYS003 Systolic Heart Failure 43 0.050
251
LKM006 Leukomalacia 43 0.050
252
BCK006 Back Pain 43 0.050
253
SXL003 Sexual Disorder 42 0.050
254
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.050
255
VNT011 Ventricular Fibrillation, Familial, 1 41 0.050
256
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.050
257
c CHR096 Chronic Pulmonary Heart Disease 40 0.050
258
HYP540 Hypertension, Diastolic 39 0.050
259
WTH001 Withdrawal Disorder 37 0.050
260
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.050
261
P ACT080 Acute Pulmonary Heart Disease 31 0.050
262
VTM003 Vitamin Metabolic Disorder 30 0.050
263
c CNT068 Central Pain Syndrome 29 0.050
264
P ENC021 Encephalopathy, Neonatal Severe 29 0.050
265
c DRR009 Diarrhea 6 29 0.050
266
RDT005 Radiation Induced Cancer 28 0.050
267
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 27 0.050
268
IMM096 Immunodeficiency 30 27 0.050
269
IMM071 Immunodeficiency 12 26 0.050
270
c PRC045 Preeclampsia/eclampsia 5 26 0.050
271
c DBT035 Diabetes Mellitus, Noninsulin-Dependent 1 25 0.050
272
c CRN174 Coronary Heart Disease 2 20 0.050
273
c CLR082 Colorectal Cancer 7 20 0.050
274
CNT010 Central Nervous System Hematologic Cancer 18 0.050
275
FRB003 Fairbank Disease 16 0.050
276
GLC077 Glucocorticoid Therapy, Response to 16 0.050
277
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.045
278
P PLM037 Pulmonary Hypertension 79 0.045
279
GST053 Gastric Cancer 78 0.045
280
P SCH015 Schizophrenia 77 0.045
281
P OVR042 Ovarian Cancer 76 0.045
282
ESP021 Esophageal Cancer 76 0.045
283
P HPT021 Hepatitis 69 0.045
284
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.045
285
P KDN017 Kidney Cancer 65 0.045
286
CNT098 Central Core Disease 65 0.045
287
P PLY011 Polycystic Ovary Syndrome 65 0.045
288
CNN005 Connective Tissue Disease 62 0.045
289
CRD119 Cardiac Arrest 61 0.045
290
TXC005 Toxic Shock Syndrome 60 0.045
291
c ACT073 Acute Leukemia 60 0.045
292
P CLR108 Colorectal Adenoma 60 0.045
293
P INF032 Infertility 59 0.045
294
P GT001 Gout 58 0.045
295
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.045
296
CTS003 Coats Disease 57 0.045
297
ABL002 Ablepharon-Macrostomia Syndrome 57 0.045
298
P INT143 Interstitial Cystitis 57 0.045
299
P OVR049 Ovarian Disease 56 0.045
300
GLC003 Glucose Intolerance 55 0.045
301
PLM010 Pulmonary Edema 54 0.045
302
P NNT009 Neonatal Diabetes Mellitus 52 0.045
303
TRM010 Traumatic Brain Injury 52 0.045
304
P OVR046 Ovarian Cyst 51 0.045
305
SPN041 Spinal Cord Disease 51 0.045
306
DYS014 Dyspepsia 50 0.045
307
FML038 Female Reproductive Organ Cancer 50 0.045
308
FML037 Female Breast Cancer 50 0.045
309
OVR063 Overnutrition 50 0.045
310
END035 Endocrine Gland Cancer 49 0.045
311
PST021 Postpartum Depression 49 0.045
312
LRN003 Learning Disability 49 0.045
313
LPD004 Lipoid Nephrosis 48 0.045
314
CHR005 Chorioamnionitis 48 0.045
315
THY030 Thyroid Gland Disease 48 0.045
316
P TRC086 Trichohepatoenteric Syndrome 1 48 0.045
317
P RNL015 Renal Hypertension 48 0.045
318
SDD007 Sudden Cardiac Death 47 0.045
319
GLT021 Glutaricaciduria, Type I 46 0.045
320
ATN004 Autonomic Neuropathy 45 0.045
321
ACD009 Acid-Labile Subunit, Deficiency of 45 0.045
322
ANX004 Anoxia 43 0.045
323
P CRD132 Cardiac Conduction Defect 43 0.045
324
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.045
325
NRN002 Neuronitis 41 0.045
326
ACT084 Acute Stress Disorder 40 0.045
327
ENT001 Enterocele 40 0.045
328
BND014 Bone Development Disease 40 0.045
329
GND003 Gonadal Disease 39 0.045
330
P HYP265 Hypotonia 38 0.045
331
PHS001 Phosphorus Metabolism Disease 38 0.045
332
NTL004 Nut Allergy 37 0.045
333
NSY001 N Syndrome 36 0.045
334
FXF002 Fox-Fordyce Disease 36 0.045
335
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.045
336
TRC026 Tracheal Disease 35 0.045
337
c PLN017 Peeling Skin Syndrome 1 34 0.045
338
PLS010 Plasma Protein Metabolism Disease 34 0.045
339
ACR002 Acrocapitofemoral Dysplasia 33 0.045
340
DSS010 Dissociative Disorder 32 0.045
341
GLB003 Globe Disease 32 0.045
342
CVT001 Cavitary Optic Disc Anomalies 31 0.045
343
FRT005 Fruit Allergy 31 0.045
344
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.045
345
ENC005 Encephalomalacia 27 0.045
346
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 27 0.045
347
SNT004 Sinoatrial Node Dysfunction and Deafness 25 0.045
348
c HYP302 Hypomagnesemia 4, Renal 24 0.045
349
c CLR081 Colorectal Cancer 6 22 0.045
350
c PLY105 Polycystic Ovary Syndrome 1 21 0.045
351
c CRN177 Coronary Heart Disease 7 20 0.045
352
ATN001 Autonomic Peripheral Neuropathy 17 0.045
353
FTL016 Fetal Edema 15 0.045
354
PRP050 Peripheral Arterial Occlusive Disease 1 14 0.045
355
P BRS047 Breast Cancer 100 0.039
356
P ALZ034 Alzheimer Disease 92 0.039
357
P MLT019 Multiple Myeloma 83 0.039
358
P ART022 Arthritis 75 0.039
359
c LKM061 Leukemia, Acute Myeloid 73 0.039
360
THY028 Thyroid Cancer 69 0.039
361
P LYM118 Lymphoma 69 0.039
362
PCK002 Pick Disease 68 0.039
363
P PNM007 Pneumonia 68 0.039
364
P PSD087 Pseudoxanthoma Elasticum 66 0.039
365
P MYL006 Myeloid Leukemia 66 0.039
366
P ART023 Arthropathy 64 0.039
367
BRN024 Bronchitis 64 0.039
368
ATS001 Autistic Disorder 63 0.039
369
SPN186 Spinal Cord Injury 63 0.039
370
P MCL013 Mucolipidosis Iv 62 0.039
371
HYP056 Hypoglycemia 61 0.039
372
HYP066 Hyperglycemia 61 0.039
373
P PNC044 Pancreatitis 61 0.039
374
ACQ007 Acquired Immunodeficiency Syndrome 60 0.039
375
P THR015 Thrombophilia 59 0.039
376
GST045 Gastroenteritis 59 0.039
377
FTT001 Fatty Liver Disease 59 0.039
378
P INT001 Intrahepatic Cholestasis 59 0.039
379
CHL068 Cholestasis 59 0.039
380
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.039
381
RHM027 Rheumatic Disease 58 0.039
382
MLG056 Malignant Hyperthermia 58 0.039
383
c FML108 Familial Breast Cancer 57 0.039
384
ADM013 Adamantinoma of Long Bones 57 0.039
385
c ACT210 Acute Respiratory Distress Syndrome 57 0.039
386
SNS001 Sensorineural Hearing Loss 57 0.039
387
HPT019 Hepatic Encephalopathy 56 0.039
388
P SCL018 Scoliosis 55 0.039
389
MGK001 Megakaryocytic Leukemia 55 0.039
390
P MNC007 Monocytic Leukemia 55 0.039
391
c THR092 Thrombophilia Due to Thrombin Defect 54 0.039
392
HDC001 Headache 54 0.039
393
P MMB011 Membranous Nephropathy 54 0.039
394
CHN016 Cohen Syndrome 54 0.039
395
MCN017 Meconium Ileus 54 0.039
396
CMP010 Complex Regional Pain Syndrome 54 0.039
397
C3D001 C3 Deficiency 53 0.039
398
HLY001 Hailey-Hailey Disease 53 0.039
399
FDL002 Food Allergy 53 0.039
400
LYM019 Lymphosarcoma 53 0.039
401
HMR039 Hemorrhage, Intracerebral 53 0.039
402
PRV006 Pervasive Developmental Disorder 53 0.039
403
P ACT105 Acute Mountain Sickness 52 0.039
404
BLR006 Biliary Tract Disease 52 0.039
405
PRS042 Prostate Disease 52 0.039
406
c ACT009 Acute Monocytic Leukemia 52 0.039
407
CLR109 Colorectal Adenocarcinoma 51 0.039
408
IMM136 Immune System Disease 51 0.039
409
GRW007 Growth Hormone Deficiency 50 0.039
410
CLN015 Colon Adenocarcinoma 50 0.039
411
P CLL015 Collagen Disease 50 0.039
412
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.039
413
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 49 0.039
414
PRN021 Paranasal Sinus Disease 49 0.039
415
PRT038 Protein-Energy Malnutrition 49 0.039
416
c INH020 Inherited Metabolic Disorder 49 0.039
417
BCL002 B Cell Deficiency 49 0.039
418
ATN005 Autonomic Dysfunction 49 0.039
419
ACT017 Acute Chest Syndrome 48 0.039
420
PLS009 Plasma Cell Neoplasm 48 0.039
421
BLD036 Bile Duct Disease 48 0.039
422
ACT098 Acute Erythroid Leukemia 47 0.039
423
GNG011 Gingival Disease 46 0.039
424
ADR038 Adermatoglyphia 46 0.039
425
SML036 Small Intestinal Adenocarcinoma 46 0.039
426
PRT082 Preterm Premature Rupture of the Membranes 46 0.039
427
c MCR113 Microvascular Complications of Diabetes 3 45 0.039
428
PRM003 Premature Ejaculation 45 0.039
429
SPS007 Spastic Cerebral Palsy 44 0.039
430
CRD118 Cardiovascular Cancer 44 0.039
431
RNL097 Renal Artery Disease 43 0.039
432
SKN027 Skin Conditions 43 0.039
433
SPS057 Spasticity 42 0.039
434
PRN019 Perinatal Necrotizing Enterocolitis 42 0.039
435
HMT008 Hematuria, Benign Familial 42 0.039
436
c CHR064 Chronic Monocytic Leukemia 42 0.039
437
ACT200 Acute Monoblastic Leukemia 42 0.039
438
OBS015 Obesity, Hyperphagia, and Developmental Delay 41 0.039
439
IRN002 Iron Metabolism Disease 41 0.039
440
PHC013 Phaeochromocytoma 41 0.039
441
SPC010 Speech and Communication Disorders 41 0.039
442
AYM001 Ayme-Gripp Syndrome 41 0.039
443
CHR413 Chronic Myocardial Ischemia 41 0.039
444
IDP070 Idiopathic Scoliosis 41 0.039
445
STT004 Steatorrhea 40 0.039
446
ADT003 Auditory System Disease 40 0.039
447
IMP006 Impulse Control Disorder 40 0.039
448
CRB086 Cerebral Aneurysms 39 0.039
449
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.039
450
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.039
451
P FML187 Familial Hypertension 38 0.039
452
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.039
453
NSL022 Nasal Cavity Disease 38 0.039
454
ADJ001 Adjustment Disorder 38 0.039
455
DRG001 Drug Psychosis 38 0.039
456
P UTR038 Uterine Disease 37 0.039
457
NNT004 Neonatal Respiratory Failure 37 0.039
458
ACT113 Acute Myeloblastic Leukemia with Maturation 37 0.039
459
MDY003 Mody, Type Ii 36 0.039
460
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.039
461
c ACT020 Acute T Cell Leukemia 35 0.039
462
HYP268 Hypercalciuria, Absorptive 35 0.039
463
INT003 Intracranial Hypotension 34 0.039
464
c BRN108 Branchiootic Syndrome 1 34 0.039
465
ANG049 Angioedema Induced by Ace Inhibitors 34 0.039
466
CRN265 Craniofacial Malformations, Asymmetric, with Polysyndactyly and Abnormal Skin and Gut Development 33 0.039
467
c CLR080 Colorectal Cancer 5 32 0.039
468
RNL021 Renal Tubular Transport Disease 32 0.039
469
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 32 0.039
470
MLD002 Mild Pre-Eclampsia 32 0.039
471
c DRR007 Diarrhea 7 31 0.039
472
RCT020 Rectum Adenocarcinoma 31 0.039
473
HNS001 Hansen's Disease 30 0.039
474
ACT118 Acute Non Lymphoblastic Leukemia 30 0.039
475
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 30 0.039
476
MRG013 Mirage Syndrome 29 0.039
477
ACT114 Acute Myeloblastic Leukemia Without Maturation 29 0.039
478
RFR004 Refractory Hematologic Cancer 28 0.039
479
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.039
480
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.039
481
c MYC058 Myocardial Infarction 2 28 0.039
482
OST097 Osteoporotic Fracture 28 0.039
483
IMM077 Immunodeficiency 20 27 0.039
484
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.039
485
HRN022 Hearing Loss/deafness 26 0.039
486
TMP008 Tempi Syndrome 22 0.039
487
INS009 Insulin-Resistance Type B 22 0.039
488
CRC034 Carcinoma Showing Thymus-Like Differentiation 21 0.039
489
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 21 0.039
490
c RNL016 Renal Infectious Disease 20 0.039
491
ACT228 Acute Radiation Syndrome 20 0.039
492
c ADL093 Adult Acute Monocytic Leukemia 19 0.039
493
VSC009 Vascular Skin Disease 19 0.039
494
c CRN176 Coronary Heart Disease 9 18 0.039
495
BNM008 Bone Mineral Density, Low 16 0.039
496
ACT179 Acute Myeloid Leukemia with 11q23 Abnormalities 15 0.039
497
WSC001 Wisconsin Syndrome 14 0.039
498
HYP646 Hypomagnesemia, Seizures, and Mental Retardation 14 0.039
499
P LNG032 Lung Cancer 95 0.031
500
P PRS040 Prostate Cancer 90 0.031
501
P OST012 Osteoarthritis 83 0.031
502
HV1006 Hiv-1 80 0.031
503
P ALG002 Alagille Syndrome 72 0.031
504
BRN028 Brain Cancer 70 0.031
505
PSY004 Psychotic Disorder 67 0.031
506
WRN001 Werner Syndrome 67 0.031
507
P END044 Endometriosis 66 0.031
508
OBS061 Obstructive Sleep Apnea 66 0.031
509
P BCL006 B-Cell Lymphomas 65 0.031
510
P AMY004 Amyloidosis 65 0.031
511
P PLR004 Pleuropulmonary Blastoma 65 0.031
512
P LNG028 Long Qt Syndrome 64 0.031
513
P THR014 Thrombocytopenia 64 0.031
514
CHR066 Chronic Fatigue Syndrome 64 0.031
515
P PRT010 Parathyroid Carcinoma 63 0.031
516
P SLP006 Sleep Apnea 61 0.031
517
LSC001 Lesch-Nyhan Syndrome 61 0.031
518
P SDD001 Sudden Infant Death Syndrome 61 0.031
519
P ADL010 Adult Respiratory Distress Syndrome 61 0.031
520
P HYP117 Hypertriglyceridemia 61 0.031
521
P NPH009 Nephrolithiasis 60 0.031
522
INT146 Intervertebral Disc Disease 60 0.031
523
WLL001 Williams-Beuren Syndrome 60 0.031
524
RBR001 Roberts Syndrome 60 0.031
525
P GRV001 Graves' Disease 59 0.031
526
MYL031 Myeloproliferative Neoplasm 58 0.031
527
ETN001 Eating Disorder 58 0.031
528
P CTR002 Cataract 58 0.031
529
P MCR010 Microcephaly 58 0.031
530
PNC034 Pancreas Disease 58 0.031
531
TRG002 Trigeminal Neuralgia 57 0.031
532
MSC077 Muscle Eye Brain Disease 57 0.031
533
P INT070 Intestinal Obstruction 57 0.031
534
PLS011 Plasmacytoma 56 0.031
535
P SML001 Small Cell Carcinoma 56 0.031
536
BRN002 Bronchiolitis 56 0.031
537
WLF001 Wolff-Parkinson-White Syndrome 56 0.031
538
JNT002 Joint Disorders 55 0.031
539
PRR007 Perry Syndrome 55 0.031
540
MCS002 Mucositis 55 0.031
541
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 55 0.031
542
VSC002 Vascular Dementia 54 0.031
543
SBS003 Substance Abuse 54 0.031
544
CND002 Conduct Disorder 54 0.031
545
P INT030 Intracranial Aneurysm 54 0.031
546
SML033 Small Cell Cancer of the Lung, Somatic 54 0.031
547
MJR011 Major Depressive Disorder and Accelerated Response to Antidepressant Drug Treatment 53 0.031
548
PYR010 Peyronie's Disease 53 0.031
549
SCT005 Scott Syndrome 53 0.031
550
ZLL002 Zollinger-Ellison Syndrome 53 0.031
551
P CNT005 Central Nervous System Lymphoma 53 0.031
552
DSS008 Disease of Mental Health 52 0.031
553
CYT008 Cytomegalovirus Infection 52 0.031
554
MYM001 Myoma 52 0.031
555
BLR001 Biliary Atresia 52 0.031
556
BLD044 Bladder Disease 51 0.031
557
ART002 Arts Syndrome 51 0.031
558
c FML053 Familial Colorectal Cancer 51 0.031
559
PTH002 Pathological Gambling 51 0.031
560
CRS005 Crest Syndrome 51 0.031
561
DSS009 Disseminated Intravascular Coagulation 51 0.031
562
BNM001 Bone Marrow Cancer 51 0.031
563
CRN030 Coronary Stenosis 51 0.031
564
MST017 Mast Cell Disease 50 0.031
565
STM007 Stomatitis 50 0.031
566
OPT003 Opiate Dependence 50 0.031
567
NNL002 Nonalcoholic Steatohepatitis 50 0.031
568
INT075 Intracranial Hypertension 50 0.031
569
c ACT134 Acute Liver Failure 50 0.031
570
HLL004 Hellp Syndrome 50 0.031
571
c PRM226 Primary Central Nervous System Lymphoma 49 0.031
572
P INT063 Intellectual Disability 49 0.031
573
MLL012 Miller Syndrome 49 0.031
574
NSD001 Nose Disease 48 0.031
575
URM002 Uremia 48 0.031
576
CRN017 Coronary Thrombosis 48 0.031
577
P HMR005 Hemorrhoid 47 0.031
578
VND001 Vein Disease 47 0.031
579
HND002 Hand, Foot and Mouth Disease 47 0.031
580
PRN009 Paranoid Schizophrenia 47 0.031
581
MGR028 Migraine with or Without Aura 1 47 0.031
582
UPP004 Upper Respiratory Tract Disease 46 0.031
583
c CLL013 Cell Type Cancer 46 0.031
584
ACH001 Acheiropody 46 0.031
585
LCT002 Lactose Intolerance 46 0.031
586
NWB001 Newborn Respiratory Distress Syndrome 45 0.031
587
BRN014 Bronchopneumonia 45 0.031
588
TCL003 T Cell Deficiency 45 0.031
589
PRP036 Peripheral T-Cell Lymphoma 45 0.031
590
MXD023 Mixed Cell Type Cancer 44 0.031
591
OCL069 Ocular Motor Apraxia 44 0.031
592
c MTR002 Mitral Valve Insufficiency 44 0.031
593
c CNT015 Central Sleep Apnea 44 0.031
594
PRM020 Premenstrual Tension 44 0.031
595
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.031
596
P SKN013 Skin Benign Neoplasm 43 0.031
597
MLR006 Male Reproductive Organ Cancer 43 0.031
598
PRD004 Prediabetes Syndrome 43 0.031
599
c HYP073 Hypersensitivity Reaction Type Iv Disease 43 0.031
600
PLS016 Plasma Cell Leukemia 42 0.031
601
NRR001 Neuroretinitis 42 0.031
602
HPT020 Hepatic Vascular Disease 42 0.031
603
APL002 Aplasia of Lacrimal and Salivary Glands 42 0.031
604
GST071 Gastrointestinal Carcinoma 42 0.031
605
EXS001 Exostosis 42 0.031
606
PRM025 Primary Bacterial Infectious Disease 41 0.031
607
VGN020 Vaginal Disease 41 0.031
608
c PRM023 Pre-Malignant Neoplasm 41 0.031
609
CNV002 Conversion Disorder 41 0.031
610
END038 Endocrine Pancreas Disease 41 0.031
611
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.031
612
c PRM212 Primary Microcephaly 40 0.031
613
HRT012 Heart Valve Disease 40 0.031
614
c PRM225 Primary Thrombocytopenia 39 0.031
615
GST093 Gastrointestinal Defects and Immunodeficiency Syndrome 39 0.031
616
EPS006 Epstein Syndrome 38 0.031
617
P ACQ009 Acquired Metabolic Disease 38 0.031
618
c HYP072 Hypersensitivity Reaction Type Iii Disease 38 0.031
619
SXD001 Sex Differentiation Disease 38 0.031
620
PRP028 Peripheral Vertigo 38 0.031
621
SNL007 Senile Cataract 37 0.031
622
c PNC106 Pancreatic Agenesis 1 37 0.031
623
c CNG031 Congenital Nervous System Abnormality 37 0.031
624
MTR007 Motor Peripheral Neuropathy 37 0.031
625
PRL008 Paralytic Ileus 37 0.031
626
VSC018 Visceral Steatosis 37 0.031
627
OCL011 Ocular Motility Disease 37 0.031
628
NNT024 Neonatal Stroke 36 0.031
629
INT078 Intracranial Thrombosis 36 0.031
630
PYR016 Pyridoxine Deficiency 36 0.031
631
FCL011 Facial Nerve Disease 36 0.031
632
c DYS119 Dystonia 9 36 0.031
633
MYT011 Myotonia 36 0.031
634
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.031
635
UTR020 Uterine Inversion 35 0.031
636
ASP004 Asphyxia Neonatorum 35 0.031
637
HMC014 Homocysteinemia 35 0.031
638
MCR011 Microinvasive Gastric Cancer 35 0.031
639
PPT001 Peptic Esophagitis 35 0.031
640
c PLM022 Pulmonary Valve Insufficiency 34 0.031
641
RDN001 Reading Disorder 34 0.031
642
MLR007 Male Reproductive System Disease 34 0.031
643
CHR028 Chronic Wasting Disease 34 0.031
644
P XLN007 X-Linked Disease 34 0.031
645
SPR024 Supratentorial Cancer 33 0.031
646
P END046 Endometritis 32 0.031
647
CRB040 Cerebrum Cancer 32 0.031
648
c ALZ031 Alzheimer Disease 17 32 0.031
649
c SNS009 Sensory Neuropathy Type 1 32 0.031
650
GST014 Gastrointestinal Lymphoma 31 0.031
651
CYT004 Cytomegalic Inclusion Disease 31 0.031
652
CYT002 Cytokine Deficiency 30 0.031
653
c OST147 Osteoarthritis 1 30 0.031
654
CBB002 Cobb Syndrome 30 0.031
655
c CLR087 Colorectal Cancer 12 30 0.031
656
ADL086 Adolescent Idiopathic Scoliosis 30 0.031
657
PDT040 Pediatric Hypertension 30 0.031
658
HRT003 Heart Lymphoma 30 0.031
659
GRN016 Grant Syndrome 29 0.031
660
INT053 Intracranial Vasospasm 28 0.031
661
WDS002 Woods Syndrome 27 0.031
662
c ADN040 Adenomas, Multiple Colorectal 27 0.031
663
GNC005 Geniculate Ganglionitis 27 0.031
664
BLR028 Biliary Atresia, Extrahepatic 27 0.031
665
IMM076 Immunodeficiency 24 27 0.031
666
c THR102 Thrombocytopenia 5 27 0.031
667
INF036 Inflammatory and Toxic Neuropathy 27 0.031
668
SML011 Smoldering Myeloma 27 0.031
669
c THR048 Thrombocytopenia 4 26 0.031
670
IMM063 Immunodeficiency 15 26 0.031
671
LRG016 Large Intestine Adenocarcinoma 26 0.031
672
PST103 Postpartum Psychosis 25 0.031
673
INT110 Intracranial Cysts 24 0.031
674
CNT017 Central Nervous System Origin Vertigo 24 0.031
675
MDR006 Moderate and Severe Traumatic Brain Injury 23 0.031
676
MCD002 Mcdonough Syndrome 23 0.031
677
DRG016 Drug Induced Dyskinesia 23 0.031
678
RSP007 Respiratory Distress Syndrome, Infant 22 0.031
679
IND003 Indolent Myeloma 22 0.031
680
PLS003 Plasmacytic Leukemia 21 0.031
681
c CHR464 Chronic Intestinal Failure 20 0.031
682
P GNR027 Generalized Peeling Skin Syndrome 19 0.031
683
ANP010 Anaplastic Plasmacytoma 19 0.031
684
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.031
685
c CLR084 Colorectal Cancer 9 17 0.031
686
RFR001 Refractory Plasma Cell Neoplasm 16 0.031
687
MGC006 Magic Syndrome 15 0.031
688
c SML023 Small Cell Lung Cancer, Adult 15 0.031
689
HRT029 Heart Tumor of the Child 15 0.031
690
NVD002 Nevada Syndrome 14 0.031
691
LYM041 Lymphocytes Absent 13 0.031
692
LRG015 Large Intestine Adenoma 12 0.031
693
TCL006 T Cell Immunodeficiency Primary 12 0.031
694
SCT004 Scott Bryant Graham Syndrome 11 0.031
695
ALM002 Aluminium Lung 9 0.031
696
HYP159 Hyperinsulinism, Focal 9 0.031
697
P RHM011 Rheumatoid Arthritis 89 0.022
698
P PNC035 Pancreatic Cancer 87 0.022
699
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.022
700
ULC004 Ulcerative Colitis 76 0.022
701
INS024 Insulin-Like Growth Factor I 75 0.022
702
MYL009 Myelodysplastic Syndrome 73 0.022
703
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.022
704
P PHC003 Pheochromocytoma 71 0.022
705
P PRK057 Parkinson Disease, Late-Onset 70 0.022
706
TBR010 Tuberculosis 70 0.022
707
c MLT136 Multiple Endocrine Neoplasia 1 69 0.022
708
P LPR003 Leprosy 69 0.022
709
LSH001 Leishmaniasis 66 0.022
710
P ATS007 Autism Spectrum Disorder 65 0.022
711
P DYS154 Dystonia 65 0.022
712
P CNJ013 Conjunctivitis 64 0.022
713
P THL005 Thalassemia 64 0.022
714
P INF037 Inflammatory Bowel Disease 63 0.022
715
RCT015 Reactive Arthritis 63 0.022
716
P MCH002 Machado-Joseph Disease 63 0.022
717
PRT036 Peritonitis 63 0.022
718
P ADD001 Addison's Disease 62 0.022
719
LPT001 Leptospirosis 62 0.022
720
VSC011 Vasculitis 62 0.022
721
P BPL003 Bipolar Disorder 62 0.022
722
FCT003 Factor X Deficiency 61 0.022
723
OST017 Osteomyelitis 61 0.022
724
EYD002 Eye Disease 61 0.022
725
P PRT013 Portal Hypertension 60 0.022
726
CLT003 Colitis 60 0.022
727
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.022
728
c VRL010 Viral Hepatitis 60 0.022
729
P PNC025 Panic Disorder 60 0.022
730
KRT001 Keratoconjunctivitis Sicca 59 0.022
731
P HMN010 Hemangioma 59 0.022
732
c HPT003 Hepatitis a 59 0.022
733
STT001 Status Epilepticus 59 0.022
734
P ALC004 Alcohol Abuse 59 0.022
735
P CMR001 Camurati-Engelmann Disease 58 0.022
736
P HYP069 Hyperparathyroidism 58 0.022
737
P MSC007 Muscle Hypertrophy 58 0.022
738
ING001 Inguinal Hernia 58 0.022
739
PST028 Post-Traumatic Stress Disorder 57 0.022
740
CRT016 Carotid Artery Disease 57 0.022
741
PNC033 Pancreas Adenocarcinoma 57 0.022
742
c SVR001 Severe Acute Respiratory Syndrome 57 0.022
743
ETH011 Ethylmalonic Encephalopathy 56 0.022
744
P FRS003 Fraser Syndrome 56 0.022
745
TRN015 Transient Cerebral Ischemia 56 0.022
746
P MLT074 Multiple Endocrine Neoplasia 56 0.022
747
P PLY019 Polyneuropathy 56 0.022
748
VSC003 Visceral Leishmaniasis 56 0.022
749
c MYT020 Myotonic Dystrophy 2 56 0.022
750
P MYP006 Myopia 56 0.022
751
c HYP615 Hyperparathyroidism, Familial Primary 56 0.022
752
LYM027 Lymphopenia 56 0.022
753
PRS047 Prostatitis 56 0.022
754
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.022
755
DBT010 Diabetic Neuropathy 55 0.022
756
THR004 Thrombocytosis 55 0.022
757
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.022
758
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.022
759
AVN001 Avian Influenza 54 0.022
760
AMY066 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 54 0.022
761
P VNS003 Venous Insufficiency 54 0.022
762
RST001 Restless Legs Syndrome 54 0.022
763
c ART101 Aortic Valve Disease 2 53 0.022
764
P MTC069 Mitochondrial Disorders 53 0.022
765
DMY004 Demyelinating Disease 53 0.022
766
P LTR001 Lateral Sclerosis 53 0.022
767
OLG003 Oligohydramnios 53 0.022
768
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 53 0.022
769
TLN003 Telangiectasis 52 0.022
770
GTR002 Goiter 52 0.022
771
P MGR003 Migraine with Aura 52 0.022
772
SSM001 Sesame Syndrome 52 0.022
773
MYC002 Mycobacterium Avium Complex Disease 52 0.022
774
RYS001 Reye Syndrome 52 0.022
775
DBT004 Diabetic Polyneuropathy 52 0.022
776
c PRK031 Parkinson Disease 1 51 0.022
777
IMP005 Impotence 51 0.022
778
P PRM006 Primary Biliary Cirrhosis 51 0.022
779
P ERY008 Erythromelalgia 51 0.022
780
c INF071 Inflammatory Bowel Disease 1 51 0.022
781
P PTS002 Ptosis 51 0.022
782
DRG011 Drug Addiction 51 0.022
783
P HRD018 Hair Disease 51 0.022
784
ALL009 Allergic Conjunctivitis 51 0.022
785
c FML023 Familial Hemiplegic Migraine 51 0.022
786
c ART115 Aortic Valve Disease 1 50 0.022
787
P HYP014 Hyperuricemia 50 0.022
788
P HYP065 Hyperaldosteronism 50 0.022
789
IMG001 Image Syndrome 50 0.022
790
DRY001 Dry Eye Syndrome 50 0.022
791
HYP037 Hyperhomocysteinemia 50 0.022
792
ANG054 Angina Pectoris 50 0.022
793
HYP006 Hypertensive Heart Disease 50 0.022
794
MSC072 Muscle Cancer 49 0.022
795
P SHR001 Short Bowel Syndrome 49 0.022
796
END021 Endomyocardial Fibrosis 49 0.022
797
ALC009 Alcoholic Liver Cirrhosis 49 0.022
798
CHL061 Childhood Leukemia 49 0.022
799
BLR007 Biliary Tract Neoplasm 49 0.022
800
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 48 0.022
801
c RTN162 Retinitis Pigmentosa 2 48 0.022
802
HMG002 Hemoglobinuria 48 0.022
803
MTN003 Motion Sickness 48 0.022
804
c PRK059 Parkinson Disease 8 48 0.022
805
OCL006 Ocular Hypertension 48 0.022
806
MSS002 Mass Syndrome 48 0.022
807
MTB004 Metabolic Acidosis 48 0.022
808
PRT029 Parathyroid Adenoma 48 0.022
809
THL018 Thalassemia Major 48 0.022
810
P CRN108 Cranioectodermal Dysplasia 1 48 0.022
811
P NGH001 Night Blindness 48 0.022
812
TCD001 Tic Disorder 48 0.022
813
BRN056 Bronchopulmonary Dysplasia 48 0.022
814
SLP001 Sleeping Sickness 48 0.022
815
P RNV001 Renovascular Hypertension 47 0.022
816
c CHR418 Chronic Leukemia 47 0.022
817
P GRN010 Granular Cell Tumor 47 0.022
818
PRM236 Primary Biliary Cholangitis 47 0.022
819
c MLG069 Malignant Hypertension 47 0.022
820
DWR001 Dwarfism 47 0.022
821
AMN002 Amino Acid Metabolic Disorder 47 0.022
822
PLP001 Pulpitis 47 0.022
823
AML029 Ameloblastoma 46 0.022
824
CNT046 Central Nervous System Vasculitis 46 0.022
825
SCL003 Social Phobia 46 0.022
826
DST006 Diastolic Heart Failure 46 0.022
827
IPX001 Ipex Syndrome 45 0.022
828
URT010 Ureteral Obstruction 45 0.022
829
P CRV039 Cervicitis 45 0.022
830
CRB016 Carbuncle 45 0.022
831
RFR010 Refractory Anemia 45 0.022
832
P HMP006 Hemiplegic Migraine 45 0.022
833
PRS045 Prostatic Hypertrophy 45 0.022
834
CHR056 Chronic Tic Disorder 44 0.022
835
MYC005 Myocardial Stunning 44 0.022
836
P LYD001 Leydig Cell Tumor 44 0.022
837
WRN002 Wernicke-Korsakoff Syndrome 44 0.022
838
c LNG096 Long Qt Syndrome 15 44 0.022
839
AGR002 Agoraphobia 44 0.022
840
PHY002 Physical Disorder 43 0.022
841
RFR003 Refractive Error 43 0.022
842
MTS001 Mutism 43 0.022
843
MCR018 Microcytic Anemia 43 0.022
844
EXC002 Exocrine Pancreatic Insufficiency 43 0.022
845
c GLC075 Glaucoma 3a, Primary Open Angle, Congenital, Juvenile, or Adult Onset 43 0.022
846
LKC003 Leukocyte Disease 43 0.022
847
WRN003 Wernicke Encephalopathy 43 0.022
848
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.022
849
CRB008 Cerebral Atherosclerosis 43 0.022
850
IDP033 Idiopathic Edema 42 0.022
851
GST030 Gastrinoma 42 0.022
852
TRC023 Trichinosis 42 0.022
853
DDN006 Duodenitis 42 0.022
854
INT071 Intestinal Perforation 42 0.022
855
PRS021 Prostatic Adenoma 42 0.022
856
MYC033 Myoclonus 42 0.022
857
ESN002 Eosinophilia-Myalgia Syndrome 42 0.022
858
FCT008 Factitious Disorder 41 0.022
859
DCB001 Decubitus Ulcer 41 0.022
860
STP004 Staphylococcal Toxic Shock Syndrome 41 0.022
861
CNT025 Central Pontine Myelinolysis 41 0.022
862
TNS007 Taeniasis 41 0.022
863
SPC005 Speech Disorder 41 0.022
864
CLV009 Clove Syndrome, Somatic 41 0.022
865
AMN006 Aminoaciduria 40 0.022
866
THL017 Thalassemia Intermedia 40 0.022
867
c PRK045 Parkinson Disease 5 40 0.022
868
DYS015 Dysentery 40 0.022
869
KWS001 Kwashiorkor 40 0.022
870
GRN006 Granulomatous Angiitis 40 0.022
871
BSL008 Basal Ganglia Disease 40 0.022
872
ATX003 Ataxia with Isolated Vitamin E Deficiency 40 0.022
873
PST053 Postherpetic Neuralgia 40 0.022
874
RTT001 Ritter's Disease 40 0.022
875
FVS001 Favism 40 0.022
876
MYF002 Myofascial Pain Syndrome 39 0.022
877
THL010 Thalassemia Minor 39 0.022
878
c HYP617 Hyperoxaluria, Primary, Type 1 39 0.022
879
HPT004 Hepatic Coma 39 0.022
880
ABD010 Abdominal Wall Defect 38 0.022
881
SCN001 Secondary Hyperparathyroidism of Renal Origin 38 0.022
882
c INF086 Inflammatory Bowel Disease 3 38 0.022
883
HYP034 Hypertensive Encephalopathy 38 0.022
884
GST007 Gastric Dilatation 38 0.022
885
P OCY001 Oocyte Maturation Defect 38 0.022
886
P HYP057 Hypervitaminosis D 38 0.022
887
BNR001 Bone Remodeling Disease 37 0.022
888
RTR001 Retrograde Amnesia 37 0.022
889
P PRX010 Paroxysmal Ventricular Fibrillation 37 0.022
890
APP016 Apple Allergy 37 0.022
891
CYC008 Cyclic Vomiting Syndrome 37 0.022
892
CNT018 Central Nervous System Leukemia 37 0.022
893
c INH004 Inherited Blood Coagulation Disease 36 0.022
894
PRS063 Paresthesia 36 0.022
895
ETH004 Euthyroid Sick Syndrome 36 0.022
896
GRV012 Grover's Disease 36 0.022
897
MTC005 Mitochondrial Metabolism Disease 36 0.022
898
ATM012 Autoimmune Disease of Blood 35 0.022
899
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 35 0.022
900
INF013 Inferior Myocardial Infarction 35 0.022
901
FCL044 Fecal Incontinence 35 0.022
902
PHB001 Phobic Disorder 34 0.022
903
c INF089 Inflammatory Bowel Disease 6 34 0.022
904
VTM001 Vitamin K Deficiency Hemorrhagic Disease 34 0.022
905
CNG064 Congenital Chloride Diarrhea 33 0.022
906
LNS003 Lens Disease 33 0.022
907
HGH001 High Pressure Neurological Syndrome 33 0.022
908
ACD004 Acdc 33 0.022
909
FNC006 Functional Gastric Disease 32 0.022
910
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 32 0.022
911
MTR028 Mitral Regurgitation, Conductive Deafness, and Fusion of Cervical Vertebrae and of Carpal and Tarsal Bones 32 0.022
912
KDN013 Kidney Hypertrophy 31 0.022
913
ASC004 Ascending Colon Cancer 31 0.022
914
c HMG004 Hemoglobin D Disease 31 0.022
915
c INF078 Inflammatory Bowel Disease 2 31 0.022
916
MDY005 Mody, Type I 30 0.022
917
FRS012 First-Degree Atrioventricular Block 30 0.022
918
c PRM039 Primary Angiitis of the Central Nervous System 30 0.022
919
P FTT008 Fatty Liver Disease, Nonalcoholic 1 30 0.022
920
c PRM032 Primary Congenital Glaucoma 30 0.022
921
AKN002 Akinetic Mutism 30 0.022
922
c PNC103 Pancreatic Cancer 4 29 0.022
923
SLL001 Sialolithiasis 29 0.022
924
c PNC111 Pancreatic Cancer 2 28 0.022
925
c SCH051 Schizophrenia 4 28 0.022
926
OSM001 Osmotic Diarrhea 28 0.022
927
WRT002 Writing Disorder 27 0.022
928
TYP027 Type 1 Diabetes Mellitus 10 27 0.022
929
c PNC094 Pancreatic Cancer 1 27 0.022
930
FNC005 Functional Colonic Disease 27 0.022
931
PRX008 Paroxysmal Cold Hemoglobinuria 26 0.022
932
c CNG478 Congenital Diarrhea 25 0.022
933
PRQ002 Paraquat Poisoning 25 0.022
934
c CLR083 Colorectal Cancer 8 24 0.022
935
KHL001 Kohler's Disease 24 0.022
936
c MLT094 Multiple Sclerosis 3 24 0.022
937
URM001 Uremic Neuropathy 24 0.022
938
TLG001 Telogen Effluvium 24 0.022
939
RVR002 Reversible Cerebral Vasoconstriction Syndrome 24 0.022
940
c CNG022 Congenital Granular Cell Tumor 24 0.022
941
c SCH056 Schizophrenia 15 23 0.022
942
CNT067 Central Cord Syndrome 23 0.022
943
NPH064 Nipah Virus Disease 22 0.022
944
ARG006 Aregenerative Anemia 22 0.022
945
ATR024 Atrial Fibrillation and Stroke 22 0.022
946
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 21 0.022
947
c INF073 Inflammatory Bowel Disease 12 21 0.022
948
NLL002 Null Syndrome 20 0.022
949
c ADL080 Adult Acute Respiratory Distress Syndrome 19 0.022
950
c SCH064 Schizophrenia 10 19 0.022
951
MNS002 Mini Stroke 19 0.022
952
MSL005 Mseleni Joint Disease 19 0.022
953
BSP001 Basophil Adenoma 18 0.022
954
c PRK058 Parkinson Disease 16 18 0.022
955
CML001 Cumulative Trauma Disorders 18 0.022
956
c MYP041 Myopia 8 18 0.022
957
c MLT093 Multiple Sclerosis 2 18 0.022
958
NN2002 Non 24 Hour Sleep Wake Disorder 18 0.022
959
OVR077 Overuse Syndrome 17 0.022
960
ZNC006 Zinc, Elevated Plasma 17 0.022
961
RST013 Restless Legs Syndrome 2 16 0.022
962
c HYP454 Hypertension, Essential 8 16 0.022
963
c FTT007 Fatty Liver Disease, Nonalcoholic 2 16 0.022
964
c BLR024 Biliary Cirrhosis, Primary, 1 16 0.022
965
MLT131 Multifocal Atrial Tachycardia 16 0.022
966
ATM053 Autoimmune Disease 2 16 0.022
967
c HYP453 Hypertension, Essential 7 15 0.022
968
ATM054 Autoimmune Disease 3 15 0.022
969
c BLR016 Biliary Cirrhosis, Primary, 2 15 0.022
970
RPT005 Repetitive Motion Disorders 15 0.022
971
SDD004 Sudden Arrhythmia Death Syndrome 15 0.022
972
c BLR025 Biliary Cirrhosis, Primary, 4 15 0.022
973
c ATS172 Autism 10 15 0.022
974
RST015 Restless Legs Syndrome 4 14 0.022
975
RST021 Restless Legs Syndrome 5 14 0.022
976
BLN008 Blind Hypotensive Eye 14 0.022
977
CGL001 Coagulation Protein Disease 14 0.022
978
LBR003 Labrador Lung 13 0.022
979
CMP052 Complication in Hemodialysis 13 0.022
980
c HMN024 Hemangioma, Hereditary 13 0.022
981
c GLC032 Glaucoma, Hereditary 13 0.022
982
RST019 Restless Legs Syndrome 8 12 0.022
983
CNT066 Central Cervical Cord Syndrome 11 0.022
984
DGT004 Digitalis Poisoning 11 0.022
985
HND012 Handigodu Joint Disease 11 0.022
986
CRN073 Coronary Arteries Congenital Malformation 10 0.022
987
MNT045 Montefiore Syndrome 10 0.022
988
c BNG034 Benign Secondary Hypertension 10 0.022
989
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 7 0.022
990
FTL013 Fetal Antihypertensive Drugs Syndrome 6 0.022
991
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 5 0.022
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