Search results for transposition of great arteries

232 hits were found for transposition of great arteries

# Family MCID Name MIFTS Score
1
CNG134 Congenitally Corrected Transposition of the Great Arteries 28 8.574
2
TRN044 Transposition of the Great Arteries 49 7.296
3
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 30 6.994
4
c TRN071 Transposition of the Great Arteries, Dextro-Looped 3 17 6.992
5
P DXT004 Dextro-Looped Transposition of the Great Arteries 38 6.824
6
ISL054 Isolated Congenitally Uncorrected Transposition of the Great Arteries 11 3.533
7
CNG259 Congenitally Uncorrected Transposition of the Great Arteries with Cardiac Malformation 7 3.499
8
CNG359 Congenitally Uncorrected Transposition of the Great Arteries with Coarctation 7 3.499
9
CNT061 Conotruncal Heart Malformations 70 3.470
10
DBL004 Double Discordia 19 0.701
11
ART140 Arteries, Anomalies of 51 0.601
12
P CRN018 Coronary Artery Anomaly 69 0.596
13
ANR040 Aneurysm 61 0.480
14
CRB009 Cerebritis 41 0.436
15
P VNT002 Ventricular Septal Defect 59 0.415
16
ISC004 Ischemia 66 0.406
17
P MYC007 Myocardial Infarction 81 0.356
18
P HRT032 Heart Disease 80 0.352
19
THR024 Thrombosis 61 0.332
20
AGN016 Aging 65 0.323
21
P CRN300 Coronary Heart Disease 1 57 0.318
22
P PLM037 Pulmonary Hypertension 79 0.313
23
c PLM164 Pulmonary Hypertension, Primary, 1 67 0.312
24
ISC006 Ischemic Heart Disease 73 0.303
25
c BLD140 Blood Group, I System 37 0.289
26
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.286
27
DXT001 Dextrocardia 55 0.266
28
P DBT009 Diabetes Mellitus 72 0.255
29
P CRV039 Cervicitis 49 0.253
30
STS002 Situs Inversus 48 0.245
31
P NRP001 Neuropathy 63 0.242
32
TRC062 Tricuspid Atresia 47 0.240
33
P BRS047 Breast Cancer 100 0.240
34
P ADN016 Adenocarcinoma 71 0.236
35
P LKM002 Leukemia 75 0.235
36
P LYM118 Lymphoma 71 0.229
37
P ART022 Arthritis 77 0.225
38
P ENC018 Encephalopathy 58 0.223
39
P TTR001 Tetralogy of Fallot 70 0.218
40
P PNC044 Pancreatitis 64 0.206
41
c ACT075 Acute Myocardial Infarction 64 0.206
42
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.199
43
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.199
44
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.199
45
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.199
46
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.199
47
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.199
48
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.199
49
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.199
50
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.199
51
HYP266 Hypoxia 61 0.198
52
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.188
53
ART016 Aortic Aneurysm 70 0.186
54
CNG034 Congestive Heart Failure 74 0.183
55
MLN008 Melanoma 72 0.181
56
P ART034 Aortopulmonary Window 25 0.180
57
P ESP024 Esophagitis 64 0.180
58
RGH006 Right Aortic Arch 25 0.177
59
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.174
60
P ATR011 Atrial Fibrillation 68 0.173
61
SQM006 Squamous Cell Carcinoma 74 0.167
62
ART031 Aortic Coarctation 48 0.166
63
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.164
64
P HYP055 Hypoplastic Left Heart Syndrome 63 0.160
65
MDS022 Mediastinitis 44 0.160
66
P NRV007 Nervous System Disease 75 0.156
67
P TRC086 Trichohepatoenteric Syndrome 1 54 0.155
68
P ALZ034 Alzheimer Disease 95 0.154
69
c HYP543 Hypoplastic Left Heart Syndrome 1 38 0.154
70
BRN071 Brain Injury 54 0.152
71
DMN002 Dementia 68 0.151
72
CRN030 Coronary Stenosis 52 0.147
73
CRT028 Cor Triatriatum 25 0.145
74
PLM070 Pulmonic Stenosis 61 0.141
75
P ATR001 Atrioventricular Septal Defect 56 0.139
76
P ANR048 Aniridia 1 68 0.139
77
SBC014 Subclavian Steal Syndrome 31 0.132
78
P END033 Endocarditis 58 0.131
79
PTN001 Patent Foramen Ovale 58 0.130
80
ANR038 Anorexia Nervosa 1 21 0.130
81
BLD137 Blood Group--Ahonen 17 0.130
82
P HYD006 Hydrocephalus 68 0.129
83
P PTN014 Patent Ductus Arteriosus 1 45 0.129
84
P ATR010 Atrial Heart Septal Defect 45 0.128
85
DDN006 Duodenitis 46 0.128
86
CRD119 Cardiac Arrest 63 0.126
87
SBP005 Subpulmonary Stenosis 14 0.125
88
VGN023 Vaginitis 59 0.124
89
P THR014 Thrombocytopenia 65 0.123
90
ART005 Arteriovenous Malformation 64 0.120
91
ATR057 Atrioventricular Block 52 0.119
92
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.117
93
CRS011 Criss-Cross Heart 24 0.117
94
CHR008 Choroiditis 47 0.115
95
c DPH024 Diaphragmatic Hernia, Congenital 63 0.112
96
P PLM064 Pulmonary Sequestration 25 0.111
97
TTL012 Total Anomalous Pulmonary Venous Return 1 42 0.109
98
HTR014 Heterotaxy, Visceral, 1, X-Linked 39 0.109
99
P TBR001 Tuberous Sclerosis 69 0.107
100
CHL065 Cholangiocarcinoma 70 0.106
101
P CRD132 Cardiac Conduction Defect 53 0.105
102
DWN001 Down Syndrome 70 0.105
103
WLF001 Wolff-Parkinson-White Syndrome 57 0.103
104
CMP035 Complete Atrioventricular Canal 27 0.103
105
c HTR021 Heterotaxy, Visceral, 5, Autosomal 28 0.102
106
LVC002 Levocardia 20 0.101
107
ALR002 Al-Raqad Syndrome 30 0.100
108
c ART101 Aortic Valve Disease 2 65 0.100
109
PLM059 Pulmonary Atresia with Ventricular Septal Defect 24 0.097
110
P LMY004 Leiomyosarcoma 59 0.096
111
EBS001 Ebstein Anomaly 52 0.096
112
HTR003 Heterotaxy 46 0.095
113
c PLM022 Pulmonary Valve Insufficiency 38 0.092
114
CYN002 Cyanosis, Transient Neonatal 32 0.092
115
P CRD224 Cardiofaciocutaneous Syndrome 1 65 0.091
116
END020 Endocardial Fibroelastosis 46 0.089
117
OST017 Osteomyelitis 64 0.088
118
MTR027 Mitral Atresia 16 0.088
119
PLG002 Plague 55 0.086
120
UNV002 Univentricular Heart 29 0.086
121
ESN011 Eisenmenger Syndrome 49 0.086
122
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.085
123
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.085
124
PLM116 Pulmonary Artery Hypoplasia 15 0.084
125
CRB037 Cerebral Palsy 70 0.083
126
VTR016 Vater/vacterl Association 37 0.083
127
BRN024 Bronchitis 67 0.083
128
P GST044 Gastritis 61 0.083
129
P CMM008 Communicating Hydrocephalus 35 0.083
130
P SCK002 Sick Sinus Syndrome 53 0.082
131
c LPM012 Lipomatosis, Multiple 64 0.082
132
MSC086 Mesocardia 14 0.081
133
P KLP003 Klippel-Feil Syndrome 46 0.081
134
TWN001 Twin-to-Twin Transfusion Syndrome 51 0.081
135
BLR001 Biliary Atresia 56 0.081
136
HPT082 Hepatic Adenomas, Familial 52 0.080
137
c ACT073 Acute Leukemia 61 0.079
138
PLM068 Pulmonary Vein Stenosis 43 0.079
139
RGH009 Right Atrial Isomerism 48 0.079
140
P TRC087 Tricuspid Valve Disease 41 0.078
141
HRT039 Heart Defects, Congenital, and Other Congenital Anomalies 30 0.078
142
P OMP004 Omphalocele 51 0.076
143
MNT266 Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects 21 0.075
144
ANS023 Anus, Imperforate 50 0.074
145
DXT002 Dextrocardia with Situs Inversus 32 0.074
146
CRT060 Cor Triatriatum Sinister 21 0.074
147
P CRC039 Coarctation of Aorta 37 0.073
148
c TRC022 Tricuspid Valve Insufficiency 36 0.073
149
ACC011 Accessory Mitral Valve Tissue 15 0.072
150
ALP046 Alport Syndrome, X-Linked 74 0.072
151
INT276 Interatrial Communication 22 0.071
152
P HLP001 Holoprosencephaly 67 0.071
153
DBL007 Double Outlet Left Ventricle 19 0.070
154
BLD163 Blood Group, Dombrock System 23 0.070
155
ART095 Aortic Valve Atresia 11 0.069
156
c ATR087 Atrial Standstill 1 59 0.069
157
INT060 Intestinal Atresia 42 0.068
158
P VSC013 Visceral Heterotaxy 45 0.068
159
KMM002 Kommerell Diverticulum 16 0.067
160
HRT011 Heart Septal Defect 44 0.067
161
AZY001 Azygos Continuation of the Inferior Vena Cava 16 0.067
162
PRX085 Preaxial Hallucal Polydactyly 23 0.066
163
c HTR023 Heterotaxy, Visceral, 6, Autosomal 19 0.066
164
HYP730 Hypogonadotropic Hypogonadism 56 0.066
165
MTR003 Mitral Valve Stenosis 45 0.065
166
STR029 Sternal Cleft 21 0.065
167
TRC037 Tracheobronchomalacia 26 0.065
168
FCL064 Facial Dysmorphism with Multiple Malformations 19 0.064
169
PTT009 Pituitary Gland Disease 56 0.064
170
GLC011 Galactose Epimerase Deficiency 46 0.064
171
PLM041 Pulmonary Valve Stenosis 48 0.064
172
KRT002 Keratomalacia 55 0.064
173
SPN331 Spondyloocular Syndrome 34 0.063
174
CHR266 Chromosome 8p23.1 Deletion 27 0.063
175
CLF027 Cleft Palate, Isolated 61 0.063
176
PRS111 Persistent Fifth Aortic Arch 15 0.061
177
P RNL100 Renal Hypodysplasia/aplasia 1 57 0.060
178
RST011 Restrictive Dermopathy, Lethal 45 0.060
179
c CRP023 Carpenter Syndrome 1 57 0.060
180
P CRN015 Cornelia De Lange Syndrome 65 0.059
181
BLD159 Blood Group, Junior System 20 0.059
182
TRC021 Tricuspid Valve Stenosis 40 0.059
183
c HTR018 Heterotaxy, Visceral, 7, Autosomal 22 0.058
184
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 57 0.058
185
FTL007 Fetal Hydantoin Syndrome 31 0.058
186
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 40 0.058
187
OSC001 Oeis Complex 31 0.057
188
SCL046 Scalp-Ear-Nipple Syndrome 34 0.057
189
THR017 Thoracoabdominal Syndrome 30 0.057
190
NLX004 Neu-Laxova Syndrome 1 49 0.057
191
CHR659 Chromosome 22q11.2 Duplication Syndrome 36 0.056
192
GNT043 Genitopalatocardiac Syndrome 22 0.056
193
P ART018 Aortic Valve Insufficiency 42 0.056
194
MCH011 Meacham Syndrome 27 0.055
195
c HTR009 Heterotaxy, Visceral, 2, Autosomal 26 0.055
196
PLM108 Pulmonary Interstitial Glycogenosis 16 0.055
197
CLB017 Coloboma, Congenital Heart Disease, Ichthyosiform Dermatosis, Mental Retardation, and Ear Anomalies Syndrome 30 0.055
198
16P008 16p11.2 Duplication 13 0.055
199
JXT004 Juxtaposition of the Atrial Appendages 9 0.055
200
16P004 16p13.11 Microduplication Syndrome 19 0.054
201
FTL058 Fetal Trimethadione Syndrome 17 0.054
202
JCK001 Jackson-Weiss Syndrome 48 0.054
203
VCT005 Vacterl Association, X-Linked, with or Without Hydrocephalus 23 0.054
204
CHR583 Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb 32 0.054
205
c CRP022 Carpenter Syndrome 2 26 0.052
206
EXS017 Exstrophy of Bladder 45 0.051
207
CTR172 Citrullinemia, Classic 58 0.049
208
KLL013 Kallmann Syndrome-Heart Disease Syndrome 15 0.048
209
SHR064 Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly 37 0.048
210
P PLM040 Pulmonary Valve Disease 38 0.047
211
PLS031 Plastic Bronchitis 28 0.046
212
46X012 46,xy Partial Gonadal Dysgenesis 41 0.046
213
MLN073 Melanosis, Neurocutaneous 38 0.046
214
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.046
215
c HYP731 Hyperaldosteronism, Familial, Type I 56 0.045
216
DBL010 Double-Orifice Mitral Valve 17 0.044
217
c CRN139 Cornelia De Lange Syndrome 1 46 0.044
218
ESP029 Esophageal Atresia/tracheoesophageal Fistula 32 0.044
219
SNG003 Single Ventricular Heart 23 0.043
220
CNG108 Congenital Mitral Stenosis 17 0.043
221
c FML001 Familial Atrial Fibrillation 55 0.043
222
P PNC045 Pancreatic Agenesis 40 0.042
223
DPH021 Diaphragm Disease 39 0.042
224
PRT048 Partial Atrioventricular Canal 32 0.041
225
ISL072 Isolated Levocardia 16 0.040
226
CRB080 Cor Biloculare 10 0.039
227
CMP084 Complete Atrioventricular Canal-Tetralogy of Fallot Syndrome 14 0.039
228
RGH003 Right Ventricle Hypoplasia 11 0.039
229
c CNG404 Congenital Heart Defects, Multiple Types, 4 17 0.039
230
CMP069 Complete Atrioventricular Canal-Ventricle Hypoplasia Syndrome 22 0.038
231
CMP070 Complete Atrioventricular Canal-Left Heart Obstruction Syndrome 15 0.038
232
THK001 Thakker-Donnai Syndrome 15 0.038
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