Search results for Magnesium

632 hits were found for Magnesium

# Family MCID Name MIFTS Score
1
P HYP210 Hypomagnesemia 2, Renal 33 6.808
2
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 19 6.783
3
HYP550 Hypomagnesemia 1, Intestinal 38 4.050
4
GTL001 Gitelman Syndrome 62 4.006
5
XLN022 X-Linked Magnesium Deficiency with Epstein-Barr Virus Infection and Neoplasia 7 3.950
6
c HYP534 Hypomagnesemia 3, Renal 37 3.282
7
MGN003 Magnesium, Elevated Red Cell 5 2.296
8
P ECL001 Eclampsia 57 0.270
9
c PRC016 Pre-Eclampsia 65 0.249
10
PNG002 Pain Agnosia 41 0.232
11
PLC008 Placenta Disease 48 0.227
12
LNG099 Lung Disease 67 0.205
13
AST005 Asthma 83 0.203
14
P PRC031 Preeclampsia/eclampsia 1 41 0.200
15
c SVR005 Severe Pre-Eclampsia 53 0.188
16
P ENC018 Encephalopathy 58 0.177
17
GST050 Gastrointestinal System Disease 66 0.175
18
ISC004 Ischemia 66 0.171
19
BRN038 Bronchial Disease 58 0.159
20
c CNT035 Central Nervous System Disease 65 0.152
21
P NRV007 Nervous System Disease 75 0.149
22
P KDN018 Kidney Disease 69 0.149
23
P HRT032 Heart Disease 80 0.147
24
RSP006 Respiratory System Disease 63 0.147
25
URN009 Urinary System Disease 58 0.147
26
VSC007 Vascular Disease 71 0.144
27
NPH003 Nephrocalcinosis 49 0.144
28
GST092 Gastroesophageal Reflux 64 0.138
29
CRB009 Cerebritis 41 0.138
30
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.133
31
P INT068 Intestinal Disease 65 0.133
32
P LVR013 Liver Disease 76 0.130
33
ANX010 Anxiety 72 0.130
34
CRB039 Cerebrovascular Disease 68 0.130
35
P CLR023 Colorectal Cancer 98 0.127
36
P DBT009 Diabetes Mellitus 72 0.127
37
ESP023 Esophageal Disease 58 0.127
38
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.127
39
P CRN300 Coronary Heart Disease 1 57 0.124
40
CLN019 Colonic Disease 55 0.124
41
BRN071 Brain Injury 54 0.124
42
ISC006 Ischemic Heart Disease 73 0.121
43
P CRN018 Coronary Artery Anomaly 69 0.121
44
P NRP001 Neuropathy 63 0.121
45
RCT017 Rectal Disease 38 0.121
46
c BLD140 Blood Group, I System 37 0.121
47
c CHR089 Chronic Kidney Failure 72 0.117
48
CRB037 Cerebral Palsy 70 0.117
49
VRL011 Viral Infectious Disease 64 0.117
50
MNT002 Mental Depression 60 0.117
51
HYP005 Hypokalemia 53 0.117
52
ART140 Arteries, Anomalies of 51 0.117
53
DYS073 Dysphagia 47 0.117
54
STT002 Status Asthmaticus 46 0.117
55
SWL001 Swallowing Disorders 36 0.117
56
P ATR011 Atrial Fibrillation 68 0.114
57
P BRS047 Breast Cancer 100 0.111
58
ADN018 Adenoma 63 0.111
59
P MYC007 Myocardial Infarction 81 0.107
60
P ESP024 Esophagitis 64 0.107
61
NRM005 Neuromuscular Disease 60 0.107
62
SPS003 Spastic Diplegia 55 0.107
63
HMG005 Hemoglobinopathy 53 0.107
64
CRD223 Cardiac Arrhythmia 52 0.107
65
P MYP004 Myopathy 69 0.104
66
P ART021 Arteriosclerosis 62 0.104
67
P DRR001 Diarrhea 60 0.104
68
NRT004 Neuritis 55 0.104
69
SCK005 Sickle Cell Disease 54 0.104
70
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.104
71
PRP019 Peripheral Nervous System Disease 53 0.104
72
CLC006 Calcinosis 51 0.104
73
HYP025 Hyperphosphatemia 48 0.104
74
END072 Endotheliitis 46 0.104
75
PRM237 Primary Hypomagnesemia 40 0.104
76
DYS011 Dyskinesia of Esophagus 39 0.104
77
MXD001 Mixed Cerebral Palsy 20 0.104
78
SCK003 Sickle Cell Anemia 73 0.100
79
HYP266 Hypoxia 61 0.100
80
TXC002 Toxic Encephalopathy 55 0.100
81
MSC033 Muscle Disorders 53 0.100
82
P CHR345 Chronic Pain 52 0.100
83
MSC004 Muscle Tissue Disease 39 0.100
84
P LKM002 Leukemia 75 0.096
85
END030 End Stage Renal Failure 59 0.096
86
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.096
87
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.096
88
P BLD051 Blood Coagulation Disease 38 0.096
89
THR024 Thrombosis 61 0.092
90
BRN004 Brain Edema 57 0.092
91
CNS004 Constipation 57 0.092
92
P MYP006 Myopia 56 0.092
93
HDN002 Head Injury 48 0.092
94
GLC008 Glucose Metabolism Disease 38 0.092
95
ADG002 Audiogenic Seizures 26 0.092
96
P ADN016 Adenocarcinoma 71 0.088
97
c ACT075 Acute Myocardial Infarction 64 0.088
98
HYP060 Hyperinsulinism 56 0.088
99
BRN080 Brain Ischemia 45 0.088
100
P HPT021 Hepatitis 75 0.083
101
IMM136 Immune System Disease 57 0.083
102
BRN106 Burns 57 0.083
103
PLC007 Placental Abruption 50 0.083
104
c TRC078 Trichohepatoenteric Syndrome 2 34 0.083
105
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.078
106
CNG034 Congestive Heart Failure 74 0.078
107
P EPL164 Epilepsy 70 0.078
108
SKN016 Skin Disease 68 0.078
109
BRS051 Breast Disease 67 0.078
110
P INF032 Infertility 59 0.078
111
LPD008 Lipid Metabolism Disorder 59 0.078
112
HDC001 Headache 55 0.078
113
P HYP024 Hypoparathyroidism 55 0.078
114
P TRC086 Trichohepatoenteric Syndrome 1 54 0.078
115
c ACT071 Acute Kidney Failure 54 0.078
116
c PNS012 Paine Syndrome 52 0.078
117
SKN027 Skin Conditions 48 0.078
118
LKM006 Leukomalacia 46 0.078
119
P OST002 Osteoporosis 75 0.073
120
LVR012 Liver Cirrhosis 73 0.073
121
PSY004 Psychotic Disorder 72 0.073
122
GST045 Gastroenteritis 65 0.073
123
AGN016 Aging 65 0.073
124
MDD011 Mood Disorder 64 0.073
125
P HYP086 Hypothyroidism 62 0.073
126
FTT001 Fatty Liver Disease 62 0.073
127
P HMR003 Hemorrhagic Disease 61 0.073
128
ANR040 Aneurysm 61 0.073
129
CHL068 Cholestasis 60 0.073
130
P THR015 Thrombophilia 58 0.073
131
PLM010 Pulmonary Edema 57 0.073
132
BNF002 Bone Fracture 56 0.073
133
MGR028 Migraine with or Without Aura 1 55 0.073
134
BLR006 Biliary Tract Disease 55 0.073
135
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.073
136
PRV004 Periventricular Leukomalacia 53 0.073
137
BLD036 Bile Duct Disease 52 0.073
138
VSC008 Vascular Hemostatic Disease 36 0.073
139
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.073
140
STR067 Stroke, Ischemic 84 0.068
141
c LKM061 Leukemia, Acute Myeloid 81 0.068
142
P ART022 Arthritis 77 0.068
143
P INF038 Influenza 77 0.068
144
PRP027 Peripheral Vascular Disease 71 0.068
145
P LYM118 Lymphoma 71 0.068
146
P MYL006 Myeloid Leukemia 69 0.068
147
DMN002 Dementia 68 0.068
148
ACQ007 Acquired Immunodeficiency Syndrome 65 0.068
149
MTH009 Mouth Disease 64 0.068
150
GST033 Gestational Diabetes 62 0.068
151
GT001 Gout 60 0.068
152
PHR003 Pharyngitis 59 0.068
153
P OVR049 Ovarian Disease 58 0.068
154
NNL002 Nonalcoholic Steatohepatitis 56 0.068
155
P SZR006 Seizure Disorder 55 0.068
156
TRM010 Traumatic Brain Injury 54 0.068
157
DYS014 Dyspepsia 54 0.068
158
CHR005 Chorioamnionitis 52 0.068
159
THY030 Thyroid Gland Disease 51 0.068
160
SNS003 Sensory Peripheral Neuropathy 48 0.068
161
P HYP265 Hypotonia 40 0.068
162
P VSC018 Visceral Steatosis 38 0.068
163
P ART106 Arterial Calcification, Generalized, of Infancy, 1 36 0.068
164
ENC005 Encephalomalacia 36 0.068
165
ACT118 Acute Non Lymphoblastic Leukemia 32 0.068
166
GND003 Gonadal Disease 32 0.068
167
HYP527 Hypomagnesemia 5, Renal, with Ocular Involvement 27 0.068
168
P ALZ034 Alzheimer Disease 95 0.062
169
OST012 Osteoarthritis 88 0.062
170
GST053 Gastric Cancer 84 0.062
171
c HYP595 Hypertension, Essential 78 0.062
172
THY028 Thyroid Cancer 72 0.062
173
BRN028 Brain Cancer 72 0.062
174
BRN024 Bronchitis 67 0.062
175
CNN005 Connective Tissue Disease 65 0.062
176
TTN003 Tetanus 65 0.062
177
P THR014 Thrombocytopenia 65 0.062
178
P PNC044 Pancreatitis 64 0.062
179
MGK001 Megakaryocytic Leukemia 63 0.062
180
BRN002 Bronchiolitis 59 0.062
181
SLP005 Sleep Disorder 59 0.062
182
P MNC007 Monocytic Leukemia 59 0.062
183
PNC034 Pancreas Disease 59 0.062
184
LYM019 Lymphosarcoma 58 0.062
185
P SCL018 Scoliosis 56 0.062
186
PRN019 Perinatal Necrotizing Enterocolitis 56 0.062
187
c LKM070 Leukemia, Acute Monocytic 55 0.062
188
P DDN001 Duodenal Ulcer 53 0.062
189
CLN015 Colon Adenocarcinoma 53 0.062
190
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 53 0.062
191
ENT011 Enterocolitis 52 0.062
192
ACT098 Acute Erythroid Leukemia 52 0.062
193
STM006 Stomach Disease 52 0.062
194
ACT017 Acute Chest Syndrome 50 0.062
195
ANX004 Anoxia 49 0.062
196
ACT200 Acute Monoblastic Leukemia 47 0.062
197
ACT058 Active Peptic Ulcer Disease 43 0.062
198
IDP070 Idiopathic Scoliosis 42 0.062
199
SPN369 Spinal Disease 42 0.062
200
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.062
201
P HYP733 Hypercalciuria, Absorptive, 2 37 0.062
202
PHS001 Phosphorus Metabolism Disease 34 0.062
203
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.062
204
ACT114 Acute Myeloblastic Leukemia Without Maturation 32 0.062
205
RCT020 Rectum Adenocarcinoma 25 0.062
206
c ADL093 Adult Acute Monocytic Leukemia 22 0.062
207
c HYP445 Hypomagnesemia 6, Renal 19 0.062
208
HYP646 Hypomagnesemia, Seizures, and Mental Retardation 17 0.062
209
P PLM037 Pulmonary Hypertension 79 0.055
210
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.055
211
P CRV035 Cervical Cancer 72 0.055
212
P SCH015 Schizophrenia 71 0.055
213
P PNM007 Pneumonia 70 0.055
214
P ATS364 Autism 70 0.055
215
P ORT004 Orthostatic Intolerance 68 0.055
216
P ALG028 Alagille Syndrome 1 68 0.055
217
P ART023 Arthropathy 68 0.055
218
P PSD087 Pseudoxanthoma Elasticum 67 0.055
219
P MCL013 Mucolipidosis Iv 67 0.055
220
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.055
221
P PLY011 Polycystic Ovary Syndrome 65 0.055
222
HYP066 Hyperglycemia 64 0.055
223
c HPT003 Hepatitis a 63 0.055
224
CRD119 Cardiac Arrest 63 0.055
225
MCS002 Mucositis 61 0.055
226
GLC003 Glucose Intolerance 58 0.055
227
HMR039 Hemorrhage, Intracerebral 57 0.055
228
BLR001 Biliary Atresia 56 0.055
229
DSS009 Disseminated Intravascular Coagulation 56 0.055
230
PST021 Postpartum Depression 54 0.055
231
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 54 0.055
232
OVR063 Overnutrition 53 0.055
233
GNR004 Generalized Anxiety Disorder 53 0.055
234
P OVR046 Ovarian Cyst 52 0.055
235
PRT082 Preterm Premature Rupture of the Membranes 51 0.055
236
PLP001 Pulpitis 50 0.055
237
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.055
238
RNL011 Renal Osteodystrophy 49 0.055
239
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.055
240
CRB085 Cerebral Hemorrhage 47 0.055
241
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.055
242
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.055
243
CRB004 Cerebral Artery Occlusion 46 0.055
244
CLN044 Colon Adenoma 45 0.055
245
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.055
246
BRN014 Bronchopneumonia 45 0.055
247
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.055
248
DCB001 Decubitus Ulcer 44 0.055
249
NRN002 Neuronitis 43 0.055
250
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.055
251
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.055
252
CRB086 Cerebral Aneurysms 42 0.055
253
OST097 Osteoporotic Fracture 41 0.055
254
FXF002 Fox-Fordyce Disease 40 0.055
255
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.055
256
MLD002 Mild Pre-Eclampsia 35 0.055
257
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 33 0.055
258
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.055
259
BLR028 Biliary Atresia, Extrahepatic 32 0.055
260
c PLY105 Polycystic Ovary Syndrome 1 30 0.055
261
RNL021 Renal Tubular Transport Disease 27 0.055
262
CRC034 Carcinoma Showing Thymus-Like Differentiation 24 0.055
263
ELS005 Elastoma 16 0.055
264
P PNC035 Pancreatic Cancer 89 0.048
265
P PRS040 Prostate Cancer 88 0.048
266
MYL069 Myeloma, Multiple 86 0.048
267
ESP021 Esophageal Cancer 79 0.048
268
c BTT014 Beta-Thalassemia 70 0.048
269
c HPT016 Hepatitis B 68 0.048
270
APN008 Apnea, Obstructive Sleep 67 0.048
271
SPN186 Spinal Cord Injury 67 0.048
272
P THL005 Thalassemia 65 0.048
273
P SLP006 Sleep Apnea 65 0.048
274
MYL031 Myeloproliferative Neoplasm 64 0.048
275
BRR014 Barrett Esophagus 64 0.048
276
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.048
277
RHM027 Rheumatic Disease 62 0.048
278
HYP056 Hypoglycemia 62 0.048
279
PRP030 Purpura 61 0.048
280
c THR092 Thrombophilia Due to Thrombin Defect 61 0.048
281
P MLG056 Malignant Hyperthermia 60 0.048
282
JNT002 Joint Disorders 60 0.048
283
SNS001 Sensorineural Hearing Loss 59 0.048
284
HPT019 Hepatic Encephalopathy 59 0.048
285
P INT030 Intracranial Aneurysm 58 0.048
286
CMP010 Complex Regional Pain Syndrome 58 0.048
287
P ACT105 Acute Mountain Sickness 58 0.048
288
ZLL002 Zollinger-Ellison Syndrome 57 0.048
289
P MCR010 Microcephaly 57 0.048
290
GST023 Gastric Ulcer 57 0.048
291
CYT008 Cytomegalovirus Infection 57 0.048
292
NPH009 Nephrolithiasis 57 0.048
293
PRS042 Prostate Disease 56 0.048
294
MYM001 Myoma 56 0.048
295
PRV006 Pervasive Developmental Disorder 56 0.048
296
c CHR320 Chiari Malformation Type I 56 0.048
297
PRM236 Primary Biliary Cholangitis 56 0.048
298
P INT070 Intestinal Obstruction 55 0.048
299
P UTR058 Uterine Anomalies 55 0.048
300
P PRM006 Primary Biliary Cirrhosis 55 0.048
301
P CLL015 Collagen Disease 53 0.048
302
HLL004 Hellp Syndrome 53 0.048
303
PRT038 Protein-Energy Malnutrition 52 0.048
304
STM007 Stomatitis 52 0.048
305
P CHL066 Cholangitis 52 0.048
306
c BNG091 Benign Chronic Pemphigus 52 0.048
307
CRV040 Cervix Carcinoma 52 0.048
308
PLS009 Plasma Cell Neoplasm 51 0.048
309
P END046 Endometritis 51 0.048
310
HND002 Hand, Foot and Mouth Disease 50 0.048
311
PRM003 Premature Ejaculation 47 0.048
312
c MTR002 Mitral Valve Insufficiency 46 0.048
313
HRT012 Heart Valve Disease 45 0.048
314
BLD053 Blood Platelet Disease 45 0.048
315
MCR011 Microinvasive Gastric Cancer 45 0.048
316
PHC013 Phaeochromocytoma 44 0.048
317
ASP004 Asphyxia Neonatorum 44 0.048
318
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 42 0.048
319
STT004 Steatorrhea 41 0.048
320
SPS057 Spasticity 41 0.048
321
PPT001 Peptic Esophagitis 40 0.048
322
CRV069 Cervix Disease 39 0.048
323
CPL005 Capillary Disease 38 0.048
324
ENT004 Enthesopathy 38 0.048
325
c BLR024 Biliary Cirrhosis, Primary, 1 35 0.048
326
CYT004 Cytomegalic Inclusion Disease 35 0.048
327
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 29 0.048
328
HPD002 Hepadnavirus Infection 14 0.048
329
P HPT023 Hepatocellular Carcinoma 94 0.039
330
P OVR042 Ovarian Cancer 82 0.039
331
P END044 Endometriosis 71 0.039
332
P RSP003 Respiratory Failure 71 0.039
333
WRN001 Werner Syndrome 70 0.039
334
P AMY004 Amyloidosis 69 0.039
335
VSC011 Vasculitis 66 0.039
336
ALC007 Alcohol Dependence 65 0.039
337
P HYP802 Hypocalcemia, Autosomal Dominant 1 64 0.039
338
P LNG028 Long Qt Syndrome 63 0.039
339
PNC033 Pancreas Adenocarcinoma 63 0.039
340
P GRV001 Graves' Disease 62 0.039
341
LSC001 Lesch-Nyhan Syndrome 62 0.039
342
NRV006 Nervous System Cancer 61 0.039
343
SDD001 Sudden Infant Death Syndrome 61 0.039
344
P CTR002 Cataract 60 0.039
345
PPT005 Peptic Ulcer Disease 60 0.039
346
TRG002 Trigeminal Neuralgia 60 0.039
347
PLS011 Plasmacytoma 60 0.039
348
VSC002 Vascular Dementia 58 0.039
349
WLF001 Wolff-Parkinson-White Syndrome 57 0.039
350
c OVR114 Ovarian Cancer 1 54 0.039
351
TCD001 Tic Disorder 54 0.039
352
c PYR010 Peyronie's Disease 54 0.039
353
PRP080 Peripheral Artery Disease 54 0.039
354
RST001 Restless Legs Syndrome 54 0.039
355
INT075 Intracranial Hypertension 53 0.039
356
URM002 Uremia 52 0.039
357
P HMR005 Hemorrhoid 51 0.039
358
P PTS002 Ptosis 50 0.039
359
PRT030 Parathyroid Gland Disease 50 0.039
360
HMC014 Homocysteinemia 49 0.039
361
PRN009 Paranoid Schizophrenia 49 0.039
362
PRM020 Premenstrual Tension 49 0.039
363
MGR001 Migraine Without Aura 47 0.039
364
PRS129 Prostatic Hyperplasia, Benign 47 0.039
365
CRB090 Cerebral Hypoxia 47 0.039
366
EXS001 Exostosis 46 0.039
367
INT071 Intestinal Perforation 44 0.039
368
MYF002 Myofascial Pain Syndrome 44 0.039
369
GST030 Gastrinoma 44 0.039
370
PLS016 Plasma Cell Leukemia 43 0.039
371
CRT015 Carotid Artery Occlusion 42 0.039
372
MYT011 Myotonia 41 0.039
373
SNL007 Senile Cataract 41 0.039
374
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.039
375
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.039
376
c ALC033 Alcohol Use Disorder 40 0.039
377
BRB001 Beriberi 40 0.039
378
SPC010 Speech and Communication Disorders 40 0.039
379
PRL008 Paralytic Ileus 38 0.039
380
DDN007 Duodenal Disease 38 0.039
381
c PLM022 Pulmonary Valve Insufficiency 38 0.039
382
LRY017 Laryngeal Disease 38 0.039
383
PYR016 Pyridoxine Deficiency 37 0.039
384
UTR020 Uterine Inversion 36 0.039
385
HRN029 Hearing Loss, Noise-Induced 33 0.039
386
CHR028 Chronic Wasting Disease 32 0.039
387
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.039
388
IND003 Indolent Myeloma 24 0.039
389
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 24 0.039
390
PLS003 Plasmacytic Leukemia 22 0.039
391
RFR001 Refractory Plasma Cell Neoplasm 19 0.039
392
P AST055 Asthma-Related Traits 1 18 0.039
393
HYP786 Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy 15 0.039
394
KRS005 Korsakoff's Amnesic Syndrome 7 0.039
395
P LNG032 Lung Cancer 99 0.028
396
P RHM011 Rheumatoid Arthritis 91 0.028
397
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.028
398
P MLT020 Multiple Sclerosis 85 0.028
399
INS024 Insulin-Like Growth Factor I 83 0.028
400
ULC004 Ulcerative Colitis 80 0.028
401
P PRK057 Parkinson Disease, Late-Onset 78 0.028
402
MYL009 Myelodysplastic Syndrome 75 0.028
403
P PHC003 Pheochromocytoma 72 0.028
404
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.028
405
LSH001 Leishmaniasis 71 0.028
406
HMN044 Human Immunodeficiency Virus Type 1 71 0.028
407
BRK010 Burkitt Lymphoma 71 0.028
408
CNN003 Conn's Syndrome 70 0.028
409
P TST021 Testicular Germ Cell Tumor 70 0.028
410
P MJR001 Major Depressive Disorder 70 0.028
411
P DBT085 Diabetes Mellitus, Insulin-Dependent 69 0.028
412
P MYC084 Mycobacterium Tuberculosis 1 69 0.028
413
P ANR048 Aniridia 1 68 0.028
414
c ATS007 Autism Spectrum Disorder 68 0.028
415
P HYD006 Hydrocephalus 68 0.028
416
P ADL010 Adult Respiratory Distress Syndrome 67 0.028
417
P CNJ013 Conjunctivitis 67 0.028
418
c SML038 Small Cell Cancer of the Lung 67 0.028
419
PRT036 Peritonitis 67 0.028
420
ATM095 Autoimmune Disease 66 0.028
421
P KDN017 Kidney Cancer 66 0.028
422
P MCR115 Microvascular Complications of Diabetes 5 66 0.028
423
LPT001 Leptospirosis 64 0.028
424
PRT010 Parathyroid Carcinoma 64 0.028
425
OST017 Osteomyelitis 64 0.028
426
KRT001 Keratoconjunctivitis Sicca 63 0.028
427
c ACT210 Acute Respiratory Distress Syndrome 63 0.028
428
RCK004 Rickets 63 0.028
429
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.028
430
P MCH002 Machado-Joseph Disease 63 0.028
431
CLT003 Colitis 63 0.028
432
P PLV020 Pelvic Organ Prolapse 63 0.028
433
P ALC004 Alcohol Abuse 63 0.028
434
FLL027 Fallopian Tube Carcinoma 62 0.028
435
P CMR001 Camurati-Engelmann Disease 62 0.028
436
P HML002 Hemolytic Anemia 62 0.028
437
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.028
438
P DYS154 Dystonia 61 0.028
439
TXC005 Toxic Shock Syndrome 61 0.028
440
P HMN010 Hemangioma 61 0.028
441
BRN056 Bronchopulmonary Dysplasia 61 0.028
442
c ACT073 Acute Leukemia 61 0.028
443
P GST044 Gastritis 61 0.028
444
P BPL003 Bipolar Disorder 61 0.028
445
c PNC108 Pancreatitis, Hereditary 60 0.028
446
AVN001 Avian Influenza 60 0.028
447
P NTR004 Neutropenia 60 0.028
448
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.028
449
STT001 Status Epilepticus 60 0.028
450
ERY003 Erythema Multiforme 60 0.028
451
DBT010 Diabetic Neuropathy 60 0.028
452
c VRL010 Viral Hepatitis 59 0.028
453
PST028 Post-Traumatic Stress Disorder 59 0.028
454
PRS047 Prostatitis 59 0.028
455
ING001 Inguinal Hernia 59 0.028
456
P LPR021 Leprosy 3 59 0.028
457
VSC003 Visceral Leishmaniasis 59 0.028
458
EMB004 Embryonal Carcinoma 59 0.028
459
TRN015 Transient Cerebral Ischemia 58 0.028
460
P HYP069 Hyperparathyroidism 58 0.028
461
P PLY019 Polyneuropathy 58 0.028
462
P SML001 Small Cell Carcinoma 58 0.028
463
P LTR001 Lateral Sclerosis 58 0.028
464
DMY004 Demyelinating Disease 58 0.028
465
P PNC025 Panic Disorder 57 0.028
466
P HYP726 Hypercalcemia, Infantile, 1 57 0.028
467
NWB001 Newborn Respiratory Distress Syndrome 56 0.028
468
c MYT020 Myotonic Dystrophy 2 56 0.028
469
LYM027 Lymphopenia 56 0.028
470
P MGR003 Migraine with Aura 56 0.028
471
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 56 0.028
472
THR004 Thrombocytosis 55 0.028
473
P HYP014 Hyperuricemia 54 0.028
474
TST014 Testicular Cancer 54 0.028
475
IMP005 Impotence 54 0.028
476
ALL009 Allergic Conjunctivitis 53 0.028
477
GTR002 Goiter 53 0.028
478
ANG054 Angina Pectoris 53 0.028
479
BLR007 Biliary Tract Neoplasm 53 0.028
480
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 53 0.028
481
ERY008 Erythromelalgia 53 0.028
482
P TRT010 Teratoma 53 0.028
483
P CRN108 Cranioectodermal Dysplasia 1 53 0.028
484
ALC009 Alcoholic Liver Cirrhosis 53 0.028
485
END040 Endogenous Depression 53 0.028
486
TLN003 Telangiectasis 52 0.028
487
HMG002 Hemoglobinuria 52 0.028
488
P SHR001 Short Bowel Syndrome 52 0.028
489
WRN002 Wernicke-Korsakoff Syndrome 52 0.028
490
MTN003 Motion Sickness 52 0.028
491
DBT004 Diabetic Polyneuropathy 51 0.028
492
END021 Endomyocardial Fibrosis 51 0.028
493
DRY001 Dry Eye Syndrome 51 0.028
494
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.028
495
SCH012 Schizoaffective Disorder 51 0.028
496
c FML023 Familial Hemiplegic Migraine 51 0.028
497
AML029 Ameloblastoma 51 0.028
498
NSD001 Nose Disease 51 0.028
499
P NGH001 Night Blindness 51 0.028
500
PRT029 Parathyroid Adenoma 50 0.028
501
CHL061 Childhood Leukemia 50 0.028
502
SCL003 Social Phobia 50 0.028
503
c RTN162 Retinitis Pigmentosa 2 50 0.028
504
CYC008 Cyclic Vomiting Syndrome 50 0.028
505
P CRV039 Cervicitis 49 0.028
506
MTB004 Metabolic Acidosis 49 0.028
507
P HMP006 Hemiplegic Migraine 49 0.028
508
c MLG069 Malignant Hypertension 49 0.028
509
CHR074 Choriocarcinoma 49 0.028
510
SMN007 Seminoma 49 0.028
511
GRN017 Granulocytopenia 49 0.028
512
URT010 Ureteral Obstruction 49 0.028
513
P RNV001 Renovascular Hypertension 48 0.028
514
CRB016 Carbuncle 48 0.028
515
DWR001 Dwarfism 48 0.028
516
RFR010 Refractory Anemia 48 0.028
517
WRN003 Wernicke Encephalopathy 47 0.028
518
MYC005 Myocardial Stunning 47 0.028
519
P CLS010 Cluster Headache 47 0.028
520
P LYD001 Leydig Cell Tumor 47 0.028
521
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 0.028
522
P CHN059 Chondrocalcinosis 47 0.028
523
AGR002 Agoraphobia 47 0.028
524
NTR018 Neutrophilia, Hereditary 46 0.028
525
c CHR418 Chronic Leukemia 46 0.028
526
ESN002 Eosinophilia-Myalgia Syndrome 46 0.028
527
VTM027 Vitamin D-Dependent Rickets, Type 2a 46 0.028
528
BCK006 Back Pain 46 0.028
529
PRD004 Prediabetes Syndrome 46 0.028
530
EPD070 Epidermoid Cysts 46 0.028
531
DDN006 Duodenitis 46 0.028
532
SPS007 Spastic Cerebral Palsy 46 0.028
533
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 45 0.028
534
CNT025 Central Pontine Myelinolysis 45 0.028
535
GRD001 Giardiasis 45 0.028
536
EXC002 Exocrine Pancreatic Insufficiency 45 0.028
537
RFR003 Refractive Error 45 0.028
538
STP004 Staphylococcal Toxic Shock Syndrome 45 0.028
539
TRC023 Trichinosis 45 0.028
540
BSL008 Basal Ganglia Disease 44 0.028
541
PST053 Postherpetic Neuralgia 44 0.028
542
TST018 Testicular Yolk Sac Tumor 44 0.028
543
P END039 Endodermal Sinus Tumor 44 0.028
544
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 44 0.028
545
P TST026 Testicular Germ Cell Cancer 44 0.028
546
DYS015 Dysentery 43 0.028
547
MCR018 Microcytic Anemia 43 0.028
548
TST015 Testicular Disease 43 0.028
549
KWS001 Kwashiorkor 43 0.028
550
c SHR030 Short Qt Syndrome 42 0.028
551
PRT035 Peritoneum Cancer 42 0.028
552
MTS001 Mutism 42 0.028
553
PHB001 Phobic Disorder 42 0.028
554
OVR112 Ovarian Germ Cell Cancer 42 0.028
555
AMN006 Aminoaciduria 41 0.028
556
c HYP794 Hyperoxaluria, Primary, Type I 41 0.028
557
TNS007 Taeniasis 41 0.028
558
c BRT042 Bartter Syndrome, Type 3 41 0.028
559
SLL001 Sialolithiasis 41 0.028
560
OLG003 Oligohydramnios 41 0.028
561
c HYP057 Hypervitaminosis D 40 0.028
562
RTR001 Retrograde Amnesia 40 0.028
563
MYC033 Myoclonus 40 0.028
564
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.028
565
HPT004 Hepatic Coma 40 0.028
566
ETH004 Euthyroid Sick Syndrome 40 0.028
567
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 40 0.028
568
MVM001 Movement Disease 40 0.028
569
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 40 0.028
570
PHT003 Phototoxic Dermatitis 39 0.028
571
P CNT036 Central Nervous System Germ Cell Tumor 39 0.028
572
c GLL024 Gallbladder Disease 1 39 0.028
573
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.028
574
FCL044 Fecal Incontinence 38 0.028
575
ART035 Arterial Calcification of Infancy 38 0.028
576
c CTR122 Cataract 5, Multiple Types 38 0.028
577
EXT001 Extragonadal Seminoma 37 0.028
578
OBS004 Obstructive Hydrocephalus 37 0.028
579
P GRM010 Germ Cells Tumors 37 0.028
580
P HRD086 Hereditary Hypophosphatemic Rickets 36 0.028
581
TST043 Testicular Seminoma 36 0.028
582
PRS063 Paresthesia 36 0.028
583
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.028
584
FLL029 Fallopian Tube Disease 35 0.028
585
NNS011 Nonseminomatous Germ Cell Tumor 35 0.028
586
PRN039 Paraneoplastic Syndromes 35 0.028
587
c MTR080 Mitral Valve Prolapse 1 34 0.028
588
HYP034 Hypertensive Encephalopathy 34 0.028
589
MNG003 Mungan Syndrome 34 0.028
590
MXD032 Mixed Germ Cell Tumor 34 0.028
591
LKC003 Leukocyte Disease 34 0.028
592
CHR076 Choriocarcinoma of the Testis 33 0.028
593
FRS012 First-Degree Atrioventricular Block 33 0.028
594
AKN002 Akinetic Mutism 33 0.028
595
GST007 Gastric Dilatation 32 0.028
596
P KLZ004 Kala-Azar 1 31 0.028
597
PRX008 Paroxysmal Cold Hemoglobinuria 30 0.028
598
ALR002 Al-Raqad Syndrome 30 0.028
599
TLG001 Telogen Effluvium 30 0.028
600
c KNN009 Kenny-Caffey Syndrome, Type 1 30 0.028
601
RSP007 Respiratory Distress Syndrome, Infant 28 0.028
602
OSM001 Osmotic Diarrhea 27 0.028
603
RVR002 Reversible Cerebral Vasoconstriction Syndrome 27 0.028
604
PRQ002 Paraquat Poisoning 27 0.028
605
EXT053 Extragonadal Nonseminomatous Germ Cell Tumor 27 0.028
606
ARG006 Aregenerative Anemia 26 0.028
607
SPR024 Supratentorial Cancer 26 0.028
608
EXT025 Extragonadal Germ Cell Cancer 25 0.028
609
EMB006 Embryonal Testis Carcinoma 25 0.028
610
HLX001 Helix Syndrome 25 0.028
611
OVR015 Ovarian Mixed Germ Cell Neoplasm 24 0.028
612
OVR077 Overuse Syndrome 23 0.028
613
BDY007 Body Mass Index Quantitative Trait Locus 1 23 0.028
614
BLD163 Blood Group, Dombrock System 23 0.028
615
CML001 Cumulative Trauma Disorders 23 0.028
616
MSL005 Mseleni Joint Disease 22 0.028
617
ANR038 Anorexia Nervosa 1 21 0.028
618
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.028
619
BSP001 Basophil Adenoma 20 0.028
620
RPT005 Repetitive Motion Disorders 20 0.028
621
URM001 Uremic Neuropathy 20 0.028
622
c CHR464 Chronic Intestinal Failure 19 0.028
623
MLT131 Multifocal Atrial Tachycardia 19 0.028
624
c HYP302 Hypomagnesemia 4, Renal 18 0.028
625
BLD137 Blood Group--Ahonen 17 0.028
626
MTR030 Mitral Valve Prolapse, Familial, X-Linked 16 0.028
627
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 15 0.028
628
RPT006 Repetitive Stress Injuries 14 0.028
629
HND012 Handigodu Joint Disease 13 0.028
630
DGT004 Digitalis Poisoning 12 0.028
631
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 11 0.028
632
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 5 0.028
Content
Loading form....