Search results for Diazoxide

446 hits were found for Diazoxide

# Family MCID Name MIFTS Score
1
HYP056 Hypoglycemia 65 26.498
2
HYP060 Hyperinsulinism 54 23.535
3
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 22.011
4
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 19.441
5
DZX005 Diazoxide-Resistant Hyperinsulinism 6 15.862
6
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 14.423
7
P HYP050 Hyperinsulinemic Hypoglycemia 57 13.736
8
DZX006 Diazoxide-Resistant Focal Hyperinsulinism 6 13.720
9
DZX003 Diazoxide-Resistant Diffuse Hyperinsulinism 4 13.720
10
DZX004 Diazoxide-Sensitive Diffuse Hyperinsulinism 5 13.720
11
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 13.433
12
HYP066 Hyperglycemia 61 11.411
13
INS001 Insulinoma 59 10.922
14
P PLM037 Pulmonary Hypertension 72 8.418
15
P HYP077 Hypertrichosis 46 6.977
16
c TYP009 Type 2 Diabetes Mellitus 92 6.898
17
HYP266 Hypoxia 57 6.271
18
ANX004 Anoxia 40 6.155
19
ISC004 Ischemia 61 5.754
20
P PLY011 Polycystic Ovary Syndrome 57 5.749
21
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 5.690
22
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.554
23
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.554
24
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.554
25
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 5.554
26
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 5.554
27
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 5.554
28
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.554
29
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 5.554
30
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.554
31
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 5.554
32
P DBT009 Diabetes Mellitus 67 5.360
33
c TYP008 Type 1 Diabetes Mellitus 70 4.942
34
P NTR004 Neutropenia 63 4.686
35
P PRD006 Prader-Willi Syndrome 61 4.603
36
P THR014 Thrombocytopenia 66 4.156
37
48X005 48,xyyy 39 4.099
38
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 48 4.089
39
MYC005 Myocardial Stunning 46 3.954
40
P BCK002 Beckwith-Wiedemann Syndrome 62 3.831
41
P ECL001 Eclampsia 52 3.764
42
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 3.755
43
P MTR004 Maturity-Onset Diabetes of the Young 68 3.610
44
CRB004 Cerebral Artery Occlusion 45 3.610
45
GLC003 Glucose Intolerance 54 3.583
46
CRN036 Craniopharyngioma 64 3.578
47
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 3.550
48
ENT011 Enterocolitis 55 3.539
49
LPD008 Lipid Metabolism Disorder 62 3.536
50
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 3.529
51
PRT037 Pertussis 65 3.493
52
CRT015 Carotid Artery Occlusion 45 3.444
53
P SZR006 Seizure Disorder 70 3.403
54
BRN071 Brain Injury 50 3.362
55
c HYP595 Hypertension, Essential 85 3.308
56
P RNV001 Renovascular Hypertension 49 3.259
57
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.250
58
ALL014 Allergic Encephalomyelitis 34 3.158
59
c SVR005 Severe Pre-Eclampsia 50 3.102
60
HYP835 Hypothalamic Obesity 38 3.102
61
c PRC016 Pre-Eclampsia 65 3.092
62
OCL069 Ocular Motor Apraxia 57 3.077
63
ISL001 Islet Cell Tumor 56 2.978
64
c MLG069 Malignant Hypertension 46 2.961
65
P RSP003 Respiratory Failure 74 2.940
66
P HYP750 Hypertriglyceridemia, Familial 62 2.895
67
HYP555 Hypertriglyceridemia, Transient Infantile 38 2.895
68
PRN019 Perinatal Necrotizing Enterocolitis 60 2.816
69
ANT039 Antisynthetase Syndrome 55 2.813
70
VLK001 Volkmann Contracture 23 2.760
71
P MLT020 Multiple Sclerosis 79 2.701
72
OST012 Osteoarthritis 77 2.701
73
ADN018 Adenoma 59 2.695
74
HYP005 Hypokalemia 55 2.695
75
c ACT071 Acute Kidney Failure 60 2.690
76
NRN004 Neuroendocrine Tumor 59 2.615
77
HPT022 Hepatoblastoma 54 2.579
78
FST010 Fasting Hypoglycemia 33 2.579
79
PRP016 Paraplegia 52 2.526
80
P LVR013 Liver Disease 69 2.514
81
P ANR048 Aniridia 1 64 2.509
82
P MJR001 Major Depressive Disorder 68 2.499
83
MNT002 Mental Depression 57 2.499
84
DPR016 Depression 65 2.499
85
P RNL015 Renal Hypertension 45 2.484
86
HMP001 Hemopericardium 47 2.484
87
P PRC012 Pericardial Effusion 50 2.484
88
c ACT027 Acute Pancreatitis 60 2.483
89
P PNC044 Pancreatitis 61 2.483
90
BRN004 Brain Edema 54 2.447
91
DMP001 Dumping Syndrome 43 2.447
92
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.413
93
c BLD140 Blood Group, I System 46 2.388
94
GLC008 Glucose Metabolism Disease 40 2.388
95
DBT084 Diabetes Mellitus, Ketosis-Prone 60 2.348
96
P HYP265 Hypotonia 42 2.343
97
CNG034 Congestive Heart Failure 69 2.304
98
P BCL017 B-Cell Lymphoma 59 2.298
99
CYS009 Cystadenoma 43 2.189
100
FTL021 Fetal Macrosomia 41 2.187
101
P TRM003 Tremor 48 2.142
102
P GLM007 Glomerulonephritis 60 2.142
103
P EXN002 Exanthem 58 2.068
104
P KBK002 Kabuki Syndrome 1 65 2.068
105
GRW007 Growth Hormone Deficiency 46 2.059
106
P KDN018 Kidney Disease 72 2.059
107
P GLY013 Glycogen Storage Disease 60 2.059
108
INS024 Insulin-Like Growth Factor I 78 1.991
109
CNT056 Cantu Syndrome 48 1.991
110
NNN035 Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome 21 1.991
111
CRB090 Cerebral Hypoxia 42 1.991
112
URM002 Uremia 47 1.966
113
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.910
114
CHR074 Choriocarcinoma 46 1.910
115
P VNT002 Ventricular Septal Defect 58 1.910
116
HRT011 Heart Septal Defect 49 1.910
117
TRN015 Transient Cerebral Ischemia 63 1.910
118
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.910
119
GST045 Gastroenteritis 58 1.910
120
HYP014 Hyperuricemia 51 1.910
121
PLC007 Placental Abruption 47 1.910
122
LYM053 Lymphomatous Thyroiditis 22 1.910
123
c PLM170 Pulmonary Venoocclusive Disease 1, Autosomal Dominant 43 1.823
124
P MTH008 Methylmalonic Acidemia 52 1.823
125
P LCT001 Lactic Acidosis 51 1.823
126
P CRD119 Cardiac Arrest 67 1.823
127
c INH020 Inherited Metabolic Disorder 48 1.823
128
ISL099 Isolated Methylmalonic Acidemia 36 1.823
129
PRT058 Pure Autonomic Failure 58 1.810
130
GST033 Gestational Diabetes 61 1.775
131
P NNT058 Neonatal Diabetes 52 1.775
132
P SCH015 Schizophrenia 74 1.730
133
HYP540 Hypertension, Diastolic 37 1.730
134
HYP017 Hypophosphatemia 49 1.730
135
ARG004 Argyria 26 1.730
136
HYP034 Hypertensive Encephalopathy 43 1.730
137
FTT001 Fatty Liver Disease 62 1.730
138
LNG099 Lung Disease 62 1.730
139
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.730
140
PRV004 Periventricular Leukomalacia 52 1.730
141
CRB039 Cerebrovascular Disease 66 1.730
142
ACT040 Acute Poststreptococcal Glomerulonephritis 36 1.730
143
PLY105 Polycystic Ovary Syndrome 1 39 1.712
144
PRL032 Perlman Syndrome 57 1.712
145
PTT009 Pituitary Gland Disease 53 1.712
146
c ACT134 Acute Liver Failure 59 1.629
147
c THR037 Thrombocytopenia 2 37 1.629
148
DFC004 Deficiency Anemia 74 1.629
149
MNC002 Munchausen by Proxy 29 1.629
150
ACT088 Acute Insulin Response 39 1.629
151
P LRY029 Laryngomalacia 48 1.629
152
c CHR684 Chronic Kidney Disease 69 1.629
153
P PRD021 Periodic Paralysis 41 1.629
155
P HYP061 Hypertrophic Cardiomyopathy 69 1.629
156
FML036 Familial Periodic Paralysis 43 1.629
157
P SHR001 Short Bowel Syndrome 53 1.629
158
CHL068 Cholestasis 61 1.629
159
STT001 Status Epilepticus 59 1.629
160
FML159 Familial Periodic Paralyses 16 1.629
161
c GLY060 Glycogen Storage Disease Ia 63 1.625
162
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.517
163
P FRD001 Friedreich Ataxia 61 1.517
164
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.517
165
HYP782 Hypoglycemia, Leucine-Induced 28 1.517
166
P CTR002 Cataract 60 1.517
167
NRN001 Neuroendocrine Carcinoma 47 1.500
168
GLC036 Glucagonoma 46 1.500
169
RTN003 Retinal Ischemia 49 1.423
170
P HYP086 Hypothyroidism 69 1.423
171
MTS004 Metastatic Insulinoma 13 1.423
172
c PLM164 Pulmonary Hypertension, Primary, 1 76 1.390
173
c ATR087 Atrial Standstill 1 74 1.390
174
ANG054 Angina Pectoris 66 1.390
175
ATR057 Atrioventricular Block 54 1.390
176
END086 End Stage Renal Disease 52 1.390
177
ALL029 Allergic Disease 59 1.390
178
c CHR098 Chronic Pyelonephritis 34 1.390
179
P PYL005 Pyelonephritis 57 1.390
180
NPH010 Nephrosclerosis 50 1.390
181
P OVR082 Overgrowth Syndrome 49 1.342
182
P TRN020 Turner Syndrome 67 1.342
183
P MLT074 Multiple Endocrine Neoplasia 59 1.342
184
P GND004 Gonadal Dysgenesis 47 1.342
185
CRB037 Cerebral Palsy 67 1.342
186
c HPT003 Hepatitis a 63 1.335
187
P HPT021 Hepatitis 69 1.335
188
P MYC007 Myocardial Infarction 70 1.255
189
MTB004 Metabolic Acidosis 48 1.239
190
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 1.239
191
PHS029 Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic 26 1.239
192
HYP043 Hyperandrogenism 48 1.239
193
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.166
194
CYS001 Cystic Fibrosis 78 1.162
195
CYN002 Cyanosis, Transient Neonatal 43 1.162
196
HRT040 Hirata Disease 38 1.162
197
ZLL002 Zollinger-Ellison Syndrome 55 1.162
198
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.162
199
c CNG411 Congenital Disorder of Glycosylation, Type in 67 1.162
200
P SKN015 Skin Carcinoma 71 1.162
201
CNS004 Constipation 56 1.162
202
P FNC004 Fanconi Syndrome 60 1.162
203
ART017 Aortic Disease 49 1.162
204
MNG006 Monogenic Diabetes 44 1.162
205
ATN005 Autonomic Dysfunction 46 1.162
206
END040 Endogenous Depression 55 1.109
207
NRT001 Neurotic Disorder 56 1.109
208
PTR034 Paternal Uniparental Disomy 19 1.061
209
P AST005 Asthma 76 1.061
210
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 1.061
211
P GST053 Gastric Cancer 83 1.061
212
c MLT156 Multiple Endocrine Neoplasia, Type I 72 1.061
213
HLX001 Helix Syndrome 48 1.061
214
ESP020 Esophageal Atresia 60 1.061
215
P HYP076 Hyperthyroidism 53 1.061
216
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.061
217
CRC006 Carcinoid Syndrome 55 1.061
218
P BRS047 Breast Cancer 98 1.043
219
TRM010 Traumatic Brain Injury 51 1.043
220
P FBR017 Fibrosarcoma 56 1.043
221
P RTN016 Retinal Degeneration 52 1.043
222
P VSC007 Vascular Disease 63 1.043
223
HMP005 Hemiplegia 54 1.043
224
P ENC018 Encephalopathy 62 1.043
225
DWR001 Dwarfism 44 1.043
226
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.949
227
VLV047 Volvulus of Midgut 52 0.949
228
WLL001 Williams-Beuren Syndrome 61 0.949
229
P BRC006 Brachydactyly 51 0.949
230
CST001 Costello Syndrome 68 0.949
231
c GRV008 Graves Disease 1 54 0.949
232
P STS008 Sotos Syndrome 1 60 0.949
233
P TRT019 Torticollis 47 0.949
234
WLF002 Wolf-Hirschhorn Syndrome 57 0.949
235
c ACT075 Acute Myocardial Infarction 56 0.949
236
GST030 Gastrinoma 45 0.949
237
CNN003 Conn's Syndrome 79 0.949
238
ASP004 Asphyxia Neonatorum 50 0.949
239
EXC002 Exocrine Pancreatic Insufficiency 42 0.949
240
CYT002 Cytokine Deficiency 43 0.949
241
CHR189 Chromosome 12p Deletion 12 0.949
242
P ALZ034 Alzheimer Disease 87 0.822
243
c GLL024 Gallbladder Disease 1 52 0.822
244
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.822
245
CRD132 Cardiac Conduction Defect 60 0.822
246
MCR037 Macroglossia 44 0.822
247
P PHC003 Pheochromocytoma 69 0.822
248
c MGR028 Migraine with or Without Aura 1 64 0.822
249
ATS010 Autosomal Recessive Disease 42 0.822
250
c MCR130 Microvascular Complications of Diabetes 6 41 0.822
251
PRT251 Proteinuria, Chronic Benign 57 0.822
252
RSP023 Rasopathy 53 0.822
253
URL001 Urolithiasis 46 0.822
254
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.822
255
FNC009 Fanconi-Bickel Syndrome 53 0.822
256
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 24 0.822
257
c MCR120 Microvascular Complications of Diabetes 7 47 0.822
258
P MDL005 Medulloblastoma 75 0.822
259
P GLM040 Glioma Susceptibility 1 71 0.822
260
HYP020 Hyperprolactinemia 63 0.822
261
ADR040 Adrenal Gland Pheochromocytoma 46 0.822
263
P HML001 Hemolytic-Uremic Syndrome 52 0.822
264
P HYP083 Hypopituitarism 52 0.822
265
SMT003 Somatostatinoma 52 0.822
266
P ALP008 Alopecia 54 0.822
267
SYN036 Syncope 45 0.822
268
ART016 Aortic Aneurysm 68 0.822
269
NPH009 Nephrolithiasis 54 0.822
270
RCK004 Rickets 68 0.822
271
c MCR113 Microvascular Complications of Diabetes 3 52 0.822
272
c MCR133 Microvascular Complications of Diabetes 4 41 0.822
273
P GRV001 Graves' Disease 55 0.822
274
P HYP069 Hyperparathyroidism 62 0.822
275
NRT004 Neuritis 53 0.822
276
MLG169 Malignant Astrocytoma 57 0.822
277
TTN003 Tetanus 65 0.822
278
P DRR001 Diarrhea 55 0.822
279
c CNT101 Central Congenital Hypothyroidism 36 0.822
280
PRS129 Prostatic Hyperplasia, Benign 49 0.671
281
c CNG415 Congenital Disorder of Glycosylation, Type Ia 59 0.671
282
c TYR012 Tyrosinemia, Type I 61 0.671
283
CHD004 Chudley-Mccullough Syndrome 48 0.671
284
P ORT004 Orthostatic Intolerance 63 0.671
285
HMH004 Hemihyperplasia, Isolated 41 0.671
286
OST159 Osteogenic Sarcoma 66 0.671
287
TST044 Testicular Torsion 45 0.671
288
HRW001 Hair Whorl 35 0.671
289
ADN072 Adenoma of Pancreas 17 0.671
290
P RNG032 Ring Chromosome 39 0.671
291
PNC006 Pancreatic Somatostatinoma 27 0.671
292
VPM001 Vipoma 49 0.671
293
PNC019 Pancreatoblastoma 38 0.671
294
GLL048 Glial Tumor 52 0.671
295
47X002 47,xyy 48 0.671
296
CLL003 Cellulitis 53 0.671
297
P INT070 Intestinal Obstruction 57 0.671
298
PRS021 Prostatic Adenoma 43 0.671
299
ATN004 Autonomic Neuropathy 42 0.671
300
PRS045 Prostatic Hypertrophy 53 0.671
301
VTM033 Vitamin K Deficiency Bleeding 48 0.671
302
PLC008 Placenta Disease 49 0.671
303
P ART021 Arteriosclerosis 54 0.671
304
P PRP029 Porphyria 60 0.671
305
PLM010 Pulmonary Edema 55 0.671
306
AMN003 Amnestic Disorder 54 0.671
307
ACT079 Acute Proliferative Glomerulonephritis 38 0.671
308
PNC008 Pancreatic Endocrine Carcinoma 39 0.671
309
P CHR345 Chronic Pain 50 0.671
310
PTT037 Pituitary Tumors 44 0.671
311
PNC049 Pancreatic Adenoma 14 0.671
312
GLM045 Glioma 63 0.671
313
P TTR001 Tetralogy of Fallot 69 0.568
314
PNC001 Pancytopenia 53 0.568
315
P ADL010 Adult Respiratory Distress Syndrome 71 0.568
316
END035 Endocrine Gland Cancer 43 0.547
317
GST057 Gastro-Enteropancreatic Neuroendocrine Tumor 16 0.547
318
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 47 0.474
319
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.474
320
CNG506 Congenital Amyoplasia 27 0.474
321
CNG491 Congenital Portosystemic Shunt 17 0.474
322
P ALP061 Alopecia, Androgenetic, 1 49 0.474
323
P CRN300 Coronary Heart Disease 1 73 0.474
324
c OTP006 Otopalatodigital Syndrome, Type I 60 0.474
325
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.474
326
SDD001 Sudden Infant Death Syndrome 60 0.474
327
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.474
328
ANR007 Anorexia Nervosa 60 0.474
329
STR067 Stroke, Ischemic 80 0.474
330
HMC014 Homocysteinemia 52 0.474
331
PPL052 Papillomatosis, Confluent and Reticulated 34 0.474
332
CLF027 Cleft Palate, Isolated 64 0.474
333
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.474
334
GST092 Gastroesophageal Reflux 61 0.474
335
BRK010 Burkitt Lymphoma 66 0.474
336
c MST023 Mesothelioma, Malignant 56 0.474
337
CHN065 Choanal Atresia, Posterior 48 0.474
338
PRP027 Peripheral Vascular Disease 71 0.474
339
SCN049 Second-Degree Atrioventricular Block 33 0.474
340
HYP003 Hypermethioninemia 51 0.474
341
LMB062 Limb Ischemia 55 0.474
342
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.474
343
RNL025 Renal Hypoplasia 41 0.474
344
P PLY014 Polycystic Kidney Disease 69 0.474
345
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.474
346
HMN047 Human Cytomegalovirus Infection 57 0.474
347
SXL003 Sexual Disorder 49 0.474
348
c CNG006 Congenital Hypothyroidism 63 0.474
349
AND014 Androgenic Alopecia 47 0.474
350
CHR103 Charge Syndrome 66 0.474
351
P PRP003 Porphyria Cutanea Tarda 66 0.474
352
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.474
353
LKN001 Leukoencephalopathy with Vanishing White Matter 63 0.474
354
LPT014 Leptin Deficiency or Dysfunction 78 0.474
355
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.474
356
ACT119 Acute Promyelocytic Leukemia 62 0.474
357
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.474
358
c PRC032 Preeclampsia/eclampsia 2 11 0.474
359
VRC005 Varicose Veins 60 0.474
360
P NLX004 Neu-Laxova Syndrome 1 55 0.474
361
c TBR025 Tuberous Sclerosis 1 84 0.474
362
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.474
363
P HNT016 Huntington Disease 73 0.474
364
INS034 Insulinomatosis and Diabetes Mellitus 26 0.474
365
GST019 Gastrointestinal Stromal Tumor 78 0.474
366
P SCL018 Scoliosis 57 0.474
367
PTT002 Potter's Syndrome 40 0.474
368
NPH003 Nephrocalcinosis 49 0.474
369
P PRM030 Permanent Neonatal Diabetes Mellitus 59 0.474
370
P FML068 Familial Hypocalciuric Hypercalcemia 55 0.474
371
P MYP006 Myopia 56 0.474
372
P NRB001 Neuroblastoma 66 0.474
373
P DYS154 Dystonia 64 0.474
374
P ART018 Aortic Valve Insufficiency 52 0.474
375
P NRP001 Neuropathy 60 0.474
376
DYS011 Dyskinesia of Esophagus 40 0.474
377
P MVM001 Movement Disease 61 0.474
378
17Q009 17q12 Recurrent Deletion Syndrome 18 0.474
379
P PTT006 Pituitary Adenoma 55 0.474
380
TLG001 Telogen Effluvium 31 0.474
381
PLC005 Placental Insufficiency 56 0.474
382
ANV001 Anovulation 47 0.474
383
P ACN011 Acne 57 0.474
384
CLR030 Clear Cell Renal Cell Carcinoma 54 0.474
385
MLG079 Malignant Pleural Mesothelioma 42 0.474
386
PPT005 Peptic Ulcer Disease 58 0.474
387
SPP007 Suppression Amblyopia 38 0.474
388
AMB002 Amblyopia 50 0.474
389
SCR003 Secretory Diarrhea 35 0.474
390
CRY001 Cryptogenic Organizing Pneumonia 54 0.474
391
P CHR071 Charcot-Marie-Tooth Disease 64 0.474
392
GTR002 Goiter 53 0.474
393
P LTR001 Lateral Sclerosis 58 0.474
394
P HMN010 Hemangioma 62 0.474
395
TXC005 Toxic Shock Syndrome 62 0.474
396
IMP005 Impotence 52 0.474
397
P DDN001 Duodenal Ulcer 53 0.474
398
PYL006 Pyloric Stenosis 48 0.474
399
P NPH012 Nephrotic Syndrome 60 0.474
400
DRG002 Drug-Induced Hepatitis 42 0.474
401
c ATM011 Autoimmune Hepatitis 63 0.474
402
CHL014 Cholera 62 0.474
403
P TBR001 Tuberous Sclerosis 69 0.474
404
P LNG028 Long Qt Syndrome 64 0.474
405
HYD002 Hydronephrosis 58 0.474
406
PRT013 Portal Hypertension 59 0.474
407
TTH006 Tooth Disease 51 0.474
408
PTS001 Patau Syndrome 56 0.474
409
CHL013 Cholecystolithiasis 37 0.474
410
c PRM005 Primary Hyperparathyroidism 59 0.474
411
HYP006 Hypertensive Heart Disease 49 0.474
412
SVR004 Severe Combined Immunodeficiency 72 0.474
413
HYD001 Hydranencephaly 43 0.474
414
MTR010 Mature Teratoma 40 0.474
415
P PRP019 Peripheral Nervous System Disease 58 0.474
416
PRT029 Parathyroid Adenoma 51 0.474
417
P PNM007 Pneumonia 67 0.474
418
P TRT010 Teratoma 51 0.474
419
P KDN017 Kidney Cancer 61 0.474
420
P BNG032 Benign Mesothelioma 53 0.474
421
P PTS002 Ptosis 52 0.474
422
GST037 Gastroparesis 52 0.474
423
LCR001 Lacrimal Duct Obstruction 27 0.474
424
HYP026 Hypoglycemic Coma 37 0.474
425
P ICH004 Ichthyosis 56 0.474
426
P MTR003 Mitral Valve Stenosis 53 0.474
427
END028 Endemic Goiter 41 0.474
428
RNL012 Renal Tuberculosis 32 0.474
429
PNC016 Pancreatic Cholera 32 0.474
430
KCN019 Kcnk9 Imprinting Syndrome 22 0.474
431
CHL150 Childhood Ataxia with Central Nervous System Hypomyelination / Vanishing White Matter 24 0.474
432
P NRF002 Neurofibromatosis 57 0.474
433
PTH003 Pathologic Nystagmus 52 0.474
434
MST020 Mast Cell Activation Syndrome 28 0.474
435
P PRC019 Precocious Puberty 47 0.474
436
SPL018 Splenomegaly 49 0.474
437
HDN002 Head Injury 44 0.474
438
P HDC001 Headache 57 0.474
439
CRB087 Cerebral Arteriosclerosis 17 0.474
440
PRS063 Paresthesia 39 0.474
441
DYS073 Dysphagia 53 0.474
442
BRN053 Bronchial Adenomas/carcinoids Childhood 22 0.474
443
BRN056 Bronchopulmonary Dysplasia 56 0.474
444
c CHR135 Charcot-Marie-Tooth Disease Type 2a 23 0.474
445
CHR178 Chromosomal Triplication 34 0.474
446
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 18 0.474
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