Search results for Ouabain

623 hits were found for Ouabain

# Family MCID Name MIFTS Score
1
OBN001 Ouabain Resistance 15 29.064
2
c HYP595 Hypertension, Essential 84 7.303
3
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 4.741
4
c MJR024 Major Affective Disorder 9 40 4.592
5
c MJR022 Major Affective Disorder 8 37 4.592
6
P BPL003 Bipolar Disorder 56 4.592
7
P NRB001 Neuroblastoma 66 3.778
8
HYP005 Hypokalemia 55 3.489
9
ANX004 Anoxia 40 3.003
10
P HYP076 Hyperthyroidism 53 2.855
11
ACT098 Acute Erythroid Leukemia 55 2.823
12
ATR057 Atrioventricular Block 54 2.785
13
P PLY014 Polycystic Kidney Disease 71 2.767
14
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 2.746
15
P MSC005 Muscular Dystrophy 66 2.637
16
P ADT009 Auditory Neuropathy Spectrum Disorder 33 2.523
17
CNG034 Congestive Heart Failure 69 2.460
18
P CRD119 Cardiac Arrest 68 2.322
19
48X005 48,xyyy 39 2.202
20
CYS001 Cystic Fibrosis 77 2.191
21
MDD011 Mood Disorder 62 2.131
22
c PRC016 Pre-Eclampsia 64 2.037
23
MSC157 Muscular Dystrophy, Duchenne Type 79 2.002
24
P SZR006 Seizure Disorder 69 1.996
25
HLX001 Helix Syndrome 47 1.992
26
P KDN018 Kidney Disease 72 1.985
27
P MLN008 Melanoma 75 1.982
28
URM002 Uremia 47 1.945
29
P LYM118 Lymphoma 69 1.939
30
c DLT002 Dilated Cardiomyopathy 79 1.931
31
P FML187 Familial Hypertension 34 1.916
32
CRD223 Cardiac Arrhythmia 63 1.906
33
BRN004 Brain Edema 54 1.885
34
TTN003 Tetanus 64 1.873
35
c ACT071 Acute Kidney Failure 60 1.858
36
CHL014 Cholera 62 1.809
37
LTH043 Lithium Transport 17 1.758
38
OST159 Osteogenic Sarcoma 66 1.688
39
ALL029 Allergic Disease 61 1.648
40
ADR040 Adrenal Gland Pheochromocytoma 45 1.647
41
P PHC003 Pheochromocytoma 70 1.647
42
OVR093 Overhydrated Hereditary Stomatocytosis 41 1.632
43
c TYP008 Type 1 Diabetes Mellitus 77 1.630
44
ANG054 Angina Pectoris 65 1.606
45
PRT037 Pertussis 49 1.577
46
PLM010 Pulmonary Edema 54 1.570
47
P BRS047 Breast Cancer 97 1.565
48
P HYP086 Hypothyroidism 69 1.562
49
GLM045 Glioma 62 1.562
50
GLL048 Glial Tumor 52 1.562
51
HPT004 Hepatic Coma 43 1.560
52
HPT019 Hepatic Encephalopathy 59 1.534
53
P LNG064 Lung Cancer Susceptibility 3 70 1.527
54
BNR002 Bone Resorption Disease 47 1.517
55
CYT002 Cytokine Deficiency 43 1.507
56
HDN002 Head Injury 44 1.440
57
DBT010 Diabetic Neuropathy 54 1.404
58
c ACT075 Acute Myocardial Infarction 55 1.401
59
ISC004 Ischemia 61 1.375
60
P HRD011 Hereditary Spherocytosis 63 1.348
61
PPL052 Papillomatosis, Confluent and Reticulated 34 1.345
62
c PCH010 Pachyonychia Congenita 3 43 1.324
63
GLB002 Glioblastoma 67 1.324
64
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.313
65
P ECL001 Eclampsia 52 1.313
66
P ENC018 Encephalopathy 62 1.301
67
HYP266 Hypoxia 56 1.292
68
ACR007 Acromegaly 70 1.291
69
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.279
70
c HYP836 Hypercholesterolemia, Familial, 1 73 1.230
71
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.190
72
P CTR002 Cataract 59 1.190
73
P RNL015 Renal Hypertension 45 1.189
74
P RNV001 Renovascular Hypertension 49 1.161
75
P MLN007 Male Infertility 56 1.161
76
THY029 Thyroid Carcinoma 54 1.161
77
P SNS001 Sensorineural Hearing Loss 59 1.160
78
HYP066 Hyperglycemia 60 1.151
79
P PLM037 Pulmonary Hypertension 69 1.145
80
HYP056 Hypoglycemia 65 1.145
81
P MYP004 Myopathy 67 1.129
82
P RTN016 Retinal Degeneration 52 1.129
83
MTB004 Metabolic Acidosis 48 1.110
84
RTN003 Retinal Ischemia 48 1.094
85
P HML001 Hemolytic-Uremic Syndrome 52 1.076
86
P PTS002 Ptosis 52 1.076
87
P TMP001 Temporal Lobe Epilepsy 49 1.076
88
P PRD021 Periodic Paralysis 42 1.066
89
c ATR087 Atrial Standstill 1 74 1.056
90
P LNG032 Lung Cancer 98 1.056
91
END040 Endogenous Depression 54 1.056
92
PLS011 Plasmacytoma 56 1.056
93
P ART021 Arteriosclerosis 53 1.056
94
P MYT002 Myotonic Dystrophy 51 1.055
95
P OVR046 Ovarian Cyst 44 1.034
96
STM007 Stomatitis 52 1.034
97
RDC003 Red Cell Phospholipid Defect with Hemolysis 16 1.033
98
PLY150 Polykaryocytosis Inducer 29 1.031
99
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.031
100
P NRP001 Neuropathy 59 1.031
101
KWS001 Kwashiorkor 44 1.019
102
TRT001 Teratocarcinoma 41 0.997
103
c MCR133 Microvascular Complications of Diabetes 4 41 0.993
104
PRT251 Proteinuria, Chronic Benign 58 0.993
105
c MCR113 Microvascular Complications of Diabetes 3 52 0.993
106
c MCR130 Microvascular Complications of Diabetes 6 41 0.993
107
c MCR120 Microvascular Complications of Diabetes 7 47 0.993
108
CHL068 Cholestasis 61 0.979
109
BLM001 Bloom Syndrome 65 0.968
110
P HPT023 Hepatocellular Carcinoma 95 0.951
111
BRN071 Brain Injury 50 0.951
112
P MTR003 Mitral Valve Stenosis 53 0.938
113
ADR016 Adrenal Cortical Carcinoma 61 0.936
114
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.936
115
P SCK002 Sick Sinus Syndrome 55 0.936
116
P HYD006 Hydrocephalus 63 0.936
117
ADR004 Adrenal Cortical Adenocarcinoma 38 0.936
118
PRT036 Peritonitis 65 0.936
119
ABT001 Abetalipoproteinemia 68 0.933
120
PRS129 Prostatic Hyperplasia, Benign 48 0.921
121
BRK010 Burkitt Lymphoma 66 0.921
122
ADR041 Adrenal Cortical Adenoma 48 0.921
123
PRS021 Prostatic Adenoma 43 0.921
124
PRS045 Prostatic Hypertrophy 52 0.921
125
MRS001 Marasmus 41 0.921
126
P FBR017 Fibrosarcoma 55 0.921
127
c SPR086 Spermatogenic Failure 3 47 0.921
128
P SCK005 Sickle Cell Disease 56 0.921
129
c TYP009 Type 2 Diabetes Mellitus 92 0.905
130
P HNT016 Huntington Disease 73 0.905
131
DFC004 Deficiency Anemia 74 0.905
132
ADT003 Auditory System Disease 49 0.905
133
P NRM002 Normal Pressure Hydrocephalus 49 0.905
134
TRM010 Traumatic Brain Injury 50 0.905
135
END086 End Stage Renal Disease 54 0.905
136
c ACT134 Acute Liver Failure 57 0.905
137
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.888
138
ESP021 Esophageal Cancer 84 0.888
139
HYP052 Hyperkalemic Periodic Paralysis 62 0.888
140
EMB004 Embryonal Carcinoma 55 0.888
141
PPL002 Papillary Carcinoma 46 0.888
142
MYT011 Myotonia 38 0.888
143
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.870
144
OCL069 Ocular Motor Apraxia 57 0.870
145
c FNC027 Fanconi Anemia, Complementation Group a 81 0.870
146
P KDN017 Kidney Cancer 60 0.870
147
SKN013 Skin Benign Neoplasm 49 0.870
148
ALD013 Aldosterone-Producing Adenoma 36 0.870
149
P LPS004 Lupus Erythematosus 61 0.870
150
GLM044 Glomerular Disease 34 0.870
151
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.851
152
P OPN001 Open-Angle Glaucoma 55 0.851
153
c FNC029 Fanconi Anemia, Complementation Group I 55 0.851
154
c SML038 Small Cell Cancer of the Lung 69 0.851
155
c DYS056 Dystonia 12 63 0.851
156
P LKM071 Leukemia, Chronic Lymphocytic 74 0.851
157
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.831
158
HMC014 Homocysteinemia 52 0.831
159
MSC007 Muscle Hypertrophy 64 0.831
160
P KLZ004 Kala-Azar 1 41 0.831
161
HMP005 Hemiplegia 53 0.831
162
P ALT001 Alternating Hemiplegia of Childhood 56 0.831
163
P BNG032 Benign Mesothelioma 53 0.831
164
ANR007 Anorexia Nervosa 59 0.831
165
WLL004 Wallerian Degeneration 38 0.831
166
LSH001 Leishmaniasis 63 0.831
167
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.810
168
P MJR007 Major Affective Disorder 1 42 0.810
169
ORL015 Oral Squamous Cell Carcinoma 43 0.810
170
P ANP001 Anaplastic Large Cell Lymphoma 61 0.810
171
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.810
172
CRB039 Cerebrovascular Disease 65 0.810
173
SQM006 Squamous Cell Carcinoma 59 0.810
174
SCH014 Schistosomiasis 56 0.810
175
P PLM036 Pulmonary Fibrosis 65 0.810
176
GST045 Gastroenteritis 58 0.810
177
P MSC003 Muscular Atrophy 52 0.810
178
P BCL017 B-Cell Lymphoma 57 0.810
179
RFR003 Refractive Error 41 0.810
180
ANX010 Anxiety 70 0.786
181
ALC007 Alcohol Dependence 65 0.786
182
P CRC039 Coarctation of Aorta 46 0.786
183
c ALT007 Alternating Hemiplegia of Childhood 2 29 0.786
184
P OPT006 Optic Nerve Disease 57 0.786
185
ADN018 Adenoma 58 0.786
186
P RTN018 Retinal Disease 53 0.786
187
c BPL002 Bipolar I Disorder 47 0.786
188
P MYL006 Myeloid Leukemia 60 0.786
189
ADL002 Adult Syndrome 69 0.778
190
ERY051 Erythroleukemia, Familial 37 0.778
191
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.778
192
c FNC030 Fanconi Anemia, Complementation Group G 38 0.778
193
ACT088 Acute Insulin Response 39 0.778
194
CYT018 Cytochrome P450 2d6 Variant 26 0.778
195
P ATX030 Ataxia-Telangiectasia 80 0.761
196
WLF001 Wolff-Parkinson-White Syndrome 63 0.761
197
DFF005 Diffuse Large B-Cell Lymphoma 55 0.761
198
P MDL005 Medulloblastoma 75 0.761
199
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.761
200
RNL077 Renal Fibrosis 46 0.761
201
CLR109 Colorectal Adenocarcinoma 50 0.761
202
c GLC092 Glaucoma, Primary Open Angle 61 0.761
203
c THR092 Thrombophilia Due to Thrombin Defect 74 0.761
204
TLN003 Telangiectasis 51 0.761
205
P LVR013 Liver Disease 68 0.761
206
P CRV031 Cervical Adenocarcinoma 48 0.761
207
FTT001 Fatty Liver Disease 61 0.761
208
HVY003 Heavy Chain Deposition Disease 17 0.761
209
HMN047 Human Cytomegalovirus Infection 59 0.731
210
WTH001 Withdrawal Disorder 47 0.731
211
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.731
212
ALC010 Alcoholic Cardiomyopathy 42 0.731
213
BRN028 Brain Cancer 73 0.731
214
P VNT002 Ventricular Septal Defect 58 0.731
215
CRN030 Coronary Stenosis 50 0.731
216
P GST053 Gastric Cancer 82 0.696
217
RCK004 Rickets 65 0.696
218
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.696
219
PHS025 Phosphatase, Acid, of Tissues 28 0.696
220
P SPN046 Spinal Muscular Atrophy 62 0.696
221
HRT011 Heart Septal Defect 49 0.696
222
P BRS044 Breast Adenocarcinoma 58 0.696
223
GST040 Gastric Adenocarcinoma 66 0.696
224
c LKM061 Leukemia, Acute Myeloid 83 0.696
225
P MRC003 Mercury Poisoning 48 0.696
226
INT075 Intracranial Hypertension 52 0.696
227
P MYS003 Myasthenia Gravis 68 0.651
228
SNT005 Sinoatrial Node Disease 47 0.651
229
SVR001 Severe Acute Respiratory Syndrome 68 0.651
230
P MYC008 Myocarditis 59 0.651
231
AMN003 Amnestic Disorder 54 0.568
232
ACT003 Acute Kidney Tubular Necrosis 46 0.542
233
HYP006 Hypertensive Heart Disease 48 0.542
234
SBV001 Subvalvular Aortic Stenosis 31 0.542
235
INS024 Insulin-Like Growth Factor I 77 0.536
236
c MGR028 Migraine with or Without Aura 1 64 0.513
237
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.513
238
P PRK039 Parkinsonism 55 0.501
239
P DYS154 Dystonia 64 0.489
240
HYP060 Hyperinsulinism 53 0.464
241
LPT001 Leptospirosis 66 0.464
242
DPH001 Diphtheria 59 0.438
243
P ADL010 Adult Respiratory Distress Syndrome 71 0.438
244
P NPH012 Nephrotic Syndrome 62 0.424
245
P GLM040 Glioma Susceptibility 1 70 0.409
246
MLG169 Malignant Astrocytoma 57 0.409
247
c MLG069 Malignant Hypertension 46 0.409
248
CHR074 Choriocarcinoma 46 0.394
249
P HML002 Hemolytic Anemia 62 0.379
250
P THL005 Thalassemia 56 0.379
251
SCK003 Sickle Cell Anemia 74 0.363
252
P HRP006 Herpes Simplex 65 0.363
253
PTH003 Pathologic Nystagmus 52 0.363
254
CGT001 Ciguatera Fish Poisoning 20 0.363
255
c BRN108 Branchiootic Syndrome 1 63 0.346
256
P THY054 Thyrotoxic Periodic Paralysis 51 0.328
257
c GRV008 Graves Disease 1 54 0.309
258
CNN003 Conn's Syndrome 77 0.309
259
P GRV001 Graves' Disease 54 0.309
260
P SKN015 Skin Carcinoma 71 0.309
261
c ALP101 Alpha-Thalassemia 62 0.309
262
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.289
263
CYS010 Cystinosis 61 0.289
264
CRB004 Cerebral Artery Occlusion 46 0.289
265
THL010 Thalassemia Minor 31 0.289
266
P FML023 Familial Hemiplegic Migraine 53 0.289
267
c MYT021 Myotonic Dystrophy 1 67 0.289
268
CRD132 Cardiac Conduction Defect 59 0.289
269
URT010 Ureteral Obstruction 45 0.289
270
P VSC007 Vascular Disease 62 0.289
271
P RHN004 Rhinitis 57 0.289
272
SPP011 Suppression of Tumorigenicity 12 61 0.289
273
c CHR684 Chronic Kidney Disease 74 0.289
274
47X002 47,xyy 48 0.289
275
HRD218 Hereditary Stomatocytosis 31 0.289
276
ALL003 Allergic Rhinitis 66 0.268
277
P CRN026 Corneal Edema 42 0.268
278
c HMG001 Hemoglobin C Disease 41 0.268
279
P MVM001 Movement Disease 61 0.268
280
c BNG021 Benign Essential Hypertension 35 0.268
281
OBS082 Obstructive Nephropathy 41 0.268
282
P TRM003 Tremor 50 0.268
283
ULC004 Ulcerative Colitis 74 0.268
284
AGN016 Aging 54 0.245
285
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.245
286
c MCR115 Microvascular Complications of Diabetes 5 65 0.245
287
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.245
288
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.245
289
SMT018 Smith-Mccort Dysplasia 2 33 0.245
290
P MGR003 Migraine with Aura 51 0.245
291
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.245
292
P DRR001 Diarrhea 55 0.245
293
P MTR012 Mitral Valve Disease 57 0.245
294
MTR002 Mitral Valve Insufficiency 51 0.245
295
HGH043 High Grade Glioma 46 0.245
296
CLN015 Colon Adenocarcinoma 64 0.245
297
c HRD198 Hereditary Dystonia 29 0.245
298
P ENC004 Encephalitis 61 0.245
299
OCL006 Ocular Hypertension 53 0.245
300
c ANM038 Anemia, Autoimmune Hemolytic 63 0.219
301
c LKM063 Leukemia, Chronic Myeloid 71 0.219
302
NRT006 North American Indian Childhood Cirrhosis 38 0.219
303
DSS032 Disease by Infectious Agent 55 0.219
304
GLC003 Glucose Intolerance 53 0.219
305
MDD018 Middle East Respiratory Syndrome 44 0.219
306
P SLP006 Sleep Apnea 69 0.219
307
c BTT014 Beta-Thalassemia 72 0.219
308
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 54 0.219
309
STT001 Status Epilepticus 58 0.219
310
P PLY019 Polyneuropathy 53 0.219
311
c SVR005 Severe Pre-Eclampsia 50 0.219
312
HMG005 Hemoglobinopathy 55 0.219
313
P INF032 Infertility 60 0.219
314
VLK001 Volkmann Contracture 22 0.219
315
PLC006 Placental Choriocarcinoma 38 0.219
316
IRN002 Iron Metabolism Disease 56 0.219
317
TXC005 Toxic Shock Syndrome 62 0.219
318
DBT007 Diabetic Cataract 35 0.219
319
JPN002 Japanese Encephalitis 61 0.219
320
P PYL005 Pyelonephritis 56 0.219
321
P LKM002 Leukemia 66 0.219
322
P LCT001 Lactic Acidosis 50 0.219
323
VCC001 Vaccinia 49 0.219
324
P MYT023 Myotonia Congenita 56 0.219
325
NRM005 Neuromuscular Disease 63 0.219
326
YLL002 Yellow Fever 61 0.219
327
CRT015 Carotid Artery Occlusion 45 0.219
328
P RTN024 Retinoblastoma 72 0.189
329
c MGR030 Migraine, Familial Hemiplegic, 2 49 0.189
330
P LKM062 Leukemia, Acute Lymphoblastic 69 0.189
331
TBL029 Tubulin, Beta 28 0.189
332
BLD170 Bladder Exstrophy and Epispadias Complex 42 0.189
333
P DNG005 Dengue Virus 55 0.189
334
P INF037 Inflammatory Bowel Disease 53 0.189
335
BCT022 Bacterial Infectious Disease 56 0.189
336
PRT013 Portal Hypertension 59 0.189
337
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.189
338
P OVR042 Ovarian Cancer 88 0.189
339
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.189
340
P LPR021 Leprosy 3 71 0.189
341
MTC205 Mitochondrial Complex Iv Deficiency, Nuclear Type 1 57 0.189
342
ZKF001 Zika Fever 51 0.189
343
HYP017 Hypophosphatemia 49 0.189
344
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.189
345
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.189
346
MNR012 Meniere Disease 55 0.189
347
HYD002 Hydronephrosis 58 0.189
348
P RSP003 Respiratory Failure 74 0.189
349
LVR012 Liver Cirrhosis 62 0.189
350
P PRP019 Peripheral Nervous System Disease 57 0.189
351
P MCR010 Microcephaly 59 0.189
352
ENT004 Enthesopathy 51 0.189
353
P LTR001 Lateral Sclerosis 58 0.189
354
HYP014 Hyperuricemia 51 0.189
355
CRB037 Cerebral Palsy 67 0.189
356
MNT002 Mental Depression 56 0.189
357
P HYP069 Hyperparathyroidism 62 0.189
358
P OBS001 Obstructive Jaundice 49 0.189
359
GTR002 Goiter 52 0.189
360
GST033 Gestational Diabetes 61 0.189
361
PRT038 Protein-Energy Malnutrition 53 0.189
362
INS001 Insulinoma 59 0.189
363
CNS004 Constipation 56 0.189
364
PRP030 Purpura 54 0.189
365
c SPR083 Sporadic Hemiplegic Migraine 28 0.189
366
ATN005 Autonomic Dysfunction 45 0.189
367
PTT037 Pituitary Tumors 44 0.189
368
P MNC007 Monocytic Leukemia 48 0.189
369
CHR178 Chromosomal Triplication 34 0.189
370
ALL014 Allergic Encephalomyelitis 34 0.189
371
FND002 Fundus Dystrophy 55 0.189
372
P MLG056 Malignant Hyperthermia 65 0.189
374
P MTC069 Mitochondrial Disorders 57 0.189
375
HNS001 Hansen's Disease 32 0.189
376
c INH030 Inherited Retinal Disorder 28 0.189
377
ART140 Arteries, Anomalies of 52 0.155
378
P BLD134 Bladder Cancer 79 0.155
379
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 57 0.155
380
DHY016 Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema 48 0.155
381
P RTN008 Retinitis Pigmentosa 79 0.155
382
SDM004 Sodium-Potassium-Atpase Activity of Red Cell 7 0.155
383
P RTN209 Retinoschisis 1, X-Linked, Juvenile 59 0.155
384
CMP087 Complement Component 7 Deficiency 37 0.155
385
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.155
386
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.155
387
P VTL001 Vitelliform Macular Dystrophy 45 0.155
388
P CRN024 Corneal Disease 43 0.155
389
NRR001 Neuroretinitis 42 0.155
390
P CHR071 Charcot-Marie-Tooth Disease 64 0.155
391
P FNC004 Fanconi Syndrome 60 0.155
392
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.155
393
c ART115 Aortic Valve Disease 1 72 0.155
394
CLC008 Colchicine Resistance 33 0.155
395
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 58 0.155
396
RTN017 Retinal Detachment 60 0.155
397
P RHM011 Rheumatoid Arthritis 81 0.155
398
P ATR011 Atrial Fibrillation 66 0.155
399
SCR003 Secretory Diarrhea 35 0.155
400
c ACT004 Acute Diarrhea 40 0.155
401
PRP080 Peripheral Artery Disease 54 0.155
402
P HYP097 Hyperekplexia 62 0.155
403
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.155
404
c LNG048 Long Qt Syndrome 3 53 0.155
405
c HNT011 Huntington Disease-Like 3 33 0.155
406
PRM057 Paramyotonia Congenita of Von Eulenburg 58 0.155
407
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.155
408
CMP060 Complement Component 9 Deficiency 32 0.155
409
AML013 Amelogenesis Imperfecta, Hypomaturation Type, Iia1 24 0.155
410
SPR004 Supravalvular Aortic Stenosis 57 0.155
411
CRY019 Cryohydrocytosis 35 0.155
412
P ALC033 Alcohol Use Disorder 67 0.155
413
BTT017 Beta-Thalassemia Major 53 0.155
414
LPD008 Lipid Metabolism Disorder 61 0.155
415
P LNG028 Long Qt Syndrome 63 0.155
416
CRV040 Cervix Carcinoma 50 0.155
417
P CYS039 Cystic Kidney Disease 52 0.155
418
c INH020 Inherited Metabolic Disorder 47 0.155
419
P ANT001 Anterolateral Myocardial Infarction 34 0.155
420
c CNG027 Congenital Hemolytic Anemia 49 0.155
421
THY030 Thyroid Gland Disease 50 0.155
422
NRN004 Neuroendocrine Tumor 55 0.155
423
PPL022 Papilloma 53 0.155
424
SNS003 Sensory Peripheral Neuropathy 51 0.155
425
P DMN002 Dementia 65 0.155
426
P PRP029 Porphyria 60 0.155
427
CHR073 Choreatic Disease 53 0.155
428
P CNG003 Congenital Dyserythropoietic Anemia 48 0.155
429
SQM002 Squamous Cell Papilloma 45 0.155
430
ALC009 Alcoholic Liver Cirrhosis 54 0.155
431
AZS001 Azoospermia 45 0.155
432
P MTH008 Methylmalonic Acidemia 52 0.155
433
NDL007 Nodular Goiter 48 0.155
434
LCH001 Leech Infestation 38 0.155
435
P ESP024 Esophagitis 60 0.155
436
P HYP061 Hypertrophic Cardiomyopathy 69 0.155
437
GST023 Gastric Ulcer 52 0.155
438
DBT008 Diabetic Angiopathy 47 0.155
439
P GLM007 Glomerulonephritis 59 0.155
440
P CHR012 Chronic Granulomatous Disease 69 0.155
441
BLR008 Bilirubin Metabolic Disorder 57 0.155
442
c SCN007 Secondary Hyperparathyroidism 51 0.155
443
RTN023 Retinitis 45 0.155
444
OVR059 Ovary Adenocarcinoma 49 0.155
445
DMY004 Demyelinating Disease 50 0.155
446
RST023 Resting Heart Rate, Variation in 40 0.155
447
EBL001 Ebola Hemorrhagic Fever 56 0.155
448
LPR001 Lepromatous Leprosy 49 0.155
449
P JVN042 Juvenile Retinoschisis 39 0.155
451
P MYC033 Myoclonus 46 0.155
452
SYN036 Syncope 44 0.155
453
ISL099 Isolated Methylmalonic Acidemia 35 0.155
454
P BRT004 Bartter Disease 58 0.155
455
HYP264 Hypertonia 36 0.155
456
THR035 Thrombasthenia 48 0.155
457
HPT022 Hepatoblastoma 54 0.155
458
P INF038 Influenza 68 0.155
459
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.155
460
GNT003 Genital Herpes 54 0.155
461
c LKM005 Leukemia, T-Cell, Chronic 33 0.155
462
ADG002 Audiogenic Seizures 25 0.155
463
PST092 Posttransplant Acute Limbic Encephalitis 29 0.155
464
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.155
465
c PRG106 Progressive Muscular Dystrophy 31 0.155
466
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 18 0.155
467
CRD137 Cardiogenic Shock 56 0.155
468
P OVR082 Overgrowth Syndrome 42 0.155
469
GST092 Gastroesophageal Reflux 60 0.109
470
FCT007 Factor Vii Deficiency 64 0.109
471
HML051 Hemolytic Anemia with Thermal Sensitivity of Red Cells 7 0.109
472
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.109
473
c GLL024 Gallbladder Disease 1 53 0.109
474
MYL069 Myeloma, Multiple 77 0.109
475
PPL058 Papilloma of Choroid Plexus 54 0.109
476
c MCL062 Mucolipidosis Ii Alpha/beta 69 0.109
477
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 65 0.109
478
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 0.109
479
c ALB021 Albinism, Oculocutaneous, Type Ii 58 0.109
480
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.109
481
DWN001 Down Syndrome 70 0.109
482
c MTC055 Mitochondrial Dna Depletion Syndrome 4b 53 0.109
483
CHK001 Chikungunya 60 0.109
484
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.109
485
c CHR678 Charcot-Marie-Tooth Disease, Axonal, Type 2dd 34 0.109
486
P FML340 Familial Episodic Pain Syndrome 50 0.109
487
P KRT007 Keratoconus 50 0.109
488
P SHR001 Short Bowel Syndrome 53 0.109
489
DNT010 Dentin Caries 31 0.109
490
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.109
491
CYS005 Cysticercosis 60 0.109
492
OTT002 Otitis Media 71 0.109
493
P GLC113 Galactosemia I 65 0.109
494
AGN003 Agenesis of the Corpus Callosum with Peripheral Neuropathy 50 0.109
495
CYS036 Cystinosis, Nephropathic 51 0.109
496
c ATS007 Autism Spectrum Disorder 72 0.109
497
P BRG001 Brugada Syndrome 69 0.109
498
P EXN002 Exanthem 58 0.109
499
STT041 Stuttering 52 0.109
500
ILT001 Ileitis 49 0.109
501
c CNG006 Congenital Hypothyroidism 63 0.109
502
TCK001 Tick-Borne Encephalitis 59 0.109
503
MTC212 Mitchell Syndrome 26 0.109
504
P MYC084 Mycobacterium Tuberculosis 1 68 0.109
505
MYT030 Myotonia, Potassium-Aggravated 47 0.109
506
P MYC007 Myocardial Infarction 69 0.109
507
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.109
508
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.109
509
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.109
510
P HYP750 Hypertriglyceridemia, Familial 62 0.109
511
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 36 0.109
512
PFF001 Pfeiffer Syndrome 77 0.109
513
ATM095 Autoimmune Disease 61 0.109
514
c MST023 Mesothelioma, Malignant 56 0.109
515
P LDD007 Liddle Syndrome 1 57 0.109
516
PLT031 Platelet Membrane Fluidity 28 0.109
517
c PRM093 Premature Ovarian Failure 7 47 0.109
518
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.109
519
RBR002 Roberts-Sc Phocomelia Syndrome 63 0.109
520
SRC027 Sarcoma, Synovial 58 0.109
521
BLL004 Bullous Keratopathy 47 0.109
522
SRC014 Sarcoma 64 0.109
523
VTM033 Vitamin K Deficiency Bleeding 50 0.109
524
RBS001 Rabies 58 0.109
525
P ART005 Arteriovenous Malformation 65 0.109
526
HRW001 Hair Whorl 35 0.109
527
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 0.109
528
INS028 Insulin Receptors, Familial Increase in 6 0.109
529
P ATS364 Autism 72 0.109
530
P TTR001 Tetralogy of Fallot 69 0.109
531
ASP038 Aspirin-Induced Respiratory Disease 16 0.109
532
P BND020 Bone Disease 60 0.109
533
CLT003 Colitis 63 0.109
534
RHD001 Rh Deficiency Syndrome 34 0.109
535
CRN019 Coronary Artery Vasospasm 47 0.109
536
P BRB001 Beriberi 44 0.109
537
GT001 Gout 63 0.109
538
EXT006 Extrahepatic Cholestasis 41 0.109
539
ACT078 Acute Porphyria 50 0.109
540
ESP023 Esophageal Disease 52 0.109
541
SVR004 Severe Combined Immunodeficiency 71 0.109
542
SCH012 Schizoaffective Disorder 49 0.109
543
KRT002 Keratomalacia 54 0.109
544
KRT008 Keratopathy 46 0.109
545
IMP005 Impotence 52 0.109
546
MCR017 Macrocytic Anemia 44 0.109
547
P HRD012 Hereditary Elliptocytosis 54 0.109
548
RTN020 Retinal Vascular Disease 45 0.109
549
P KRN004 Kernicterus 47 0.109
550
DBT004 Diabetic Polyneuropathy 50 0.109
551
P CRD246 Cardiovascular System Disease 55 0.109
552
P RNL007 Renal Tubular Acidosis 52 0.109
553
DMP001 Dumping Syndrome 43 0.109
554
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.109
555
P HYP024 Hypoparathyroidism 55 0.109
556
c PRM005 Primary Hyperparathyroidism 59 0.109
557
HMS001 Hemosiderosis 48 0.109
558
IRN001 Iron Deficiency Anemia 58 0.109
559
PLR008 Pleurisy 49 0.109
560
FML036 Familial Periodic Paralysis 43 0.109
561
CHL004 Cholelithiasis 48 0.109
562
FCH001 Fuchs' Endothelial Dystrophy 48 0.109
563
TST014 Testicular Cancer 51 0.109
564
GNG012 Gingival Overgrowth 49 0.109
565
SKN022 Skin Squamous Cell Carcinoma 54 0.109
566
P RHB003 Rhabdomyosarcoma 66 0.109
567
P EPD016 Epidermolysis Bullosa 53 0.109
568
MCL006 Macular Retinal Edema 56 0.109
569
P PSD003 Pseudohypoaldosteronism 45 0.109
570
INT010 Intracranial Embolism 48 0.109
571
ENM001 Enamel Caries 27 0.109
572
OCL009 Ocular Cancer 55 0.109
573
P THY023 Thymoma 64 0.109
574
c MCP050 Mucopolysaccharidosis, Type Ii 73 0.109
575
P RTT002 Rett Syndrome 79 0.109
576
P PNC035 Pancreatic Cancer 86 0.109
577
LKR002 Leukoregulin 27 0.109
578
P ORT004 Orthostatic Intolerance 62 0.109
579
GLC022 Glucose/galactose Malabsorption 44 0.109
580
c RTN047 Retinitis Pigmentosa 18 45 0.109
581
c THY107 Thymoma, Familial 42 0.109
582
DPR016 Depression 65 0.109
583
CRB090 Cerebral Hypoxia 42 0.109
584
SPN035 Spindle Cell Sarcoma 51 0.109
585
BRS050 Breast Cyst 38 0.109
586
PRS064 Persistent Vegetative State 33 0.109
587
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 39 0.109
588
HRD103 Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum 13 0.109
589
LNG099 Lung Disease 62 0.109
590
SNL007 Senile Cataract 40 0.109
591
P EYD002 Eye Disease 57 0.109
592
UNL002 Unilateral Retinoblastoma 37 0.109
593
INT082 Intraocular Retinoblastoma 29 0.109
594
P RBL001 Rubella 58 0.109
595
SPN186 Spinal Cord Injury 61 0.109
596
FML159 Familial Periodic Paralyses 16 0.109
597
P FBR031 Febrile Seizures 52 0.109
598
BRN056 Bronchopulmonary Dysplasia 57 0.109
599
AMN006 Aminoaciduria 37 0.109
600
INT007 Intermediate Coronary Syndrome 53 0.109
601
DBT006 Diabetic Macular Edema 48 0.109
602
OST012 Osteoarthritis 77 0.109
603
DVR002 Diverticulitis 46 0.109
604
PPT005 Peptic Ulcer Disease 58 0.109
605
SKN019 Skin Melanoma 70 0.109
606
CCN002 Cocaine Abuse 49 0.109
607
HYP034 Hypertensive Encephalopathy 43 0.109
608
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 0.109
609
GRW007 Growth Hormone Deficiency 47 0.109
610
GLC036 Glucagonoma 45 0.109
611
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.109
612
DWR001 Dwarfism 45 0.109
613
HYP835 Hypothalamic Obesity 38 0.109
614
P PMP001 Pemphigus 55 0.109
615
P ACT105 Acute Mountain Sickness 52 0.109
616
PYR016 Pyridoxine Deficiency 29 0.109
617
IDP042 Idiopathic Recurrent Stupor 8 0.109
619
c FML306 Familial or Sporadic Hemiplegic Migraine 37 0.109
620
P RRH023 Rare Hereditary Hemochromatosis 53 0.109
621
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.109
622
ARG004 Argyria 26 0.109
623
MTH086 Methotrexate Toxicity 32 0.109
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