Search results for "transposition of great arteries"

The MalaCard for "transposition of great arteries" has been retired.
Searching MalaCards for entries containing "transposition of great arteries"

203 hits were found for 'transposition of great arteries'

# Family MCID Name MIFTS Score
1
CNG134 Congenitally Corrected Transposition of the Great Arteries 25 8.089
2
TRN044 Transposition of the Great Arteries 48 7.846
3
P TRN035 Transposition of Great Arteries, Dextro-Looped 3 18 5.967
4
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 22 5.887
5
c TRN036 Transposition of the Great Arteries, Dextro-Looped 2 12 4.616
6
CNG422 Congenitally Uncorrected Transposition of the Great Arteries 13 3.605
7
CNG259 Congenitally Uncorrected Transposition of the Great Arteries with Cardiac Malformation 5 3.517
8
CNG359 Congenitally Uncorrected Transposition of the Great Arteries with Coarctation 5 3.517
9
ISL054 Isolated Congenitally Uncorrected Transposition of the Great Arteries 5 3.517
10
P CNT061 Conotruncal Heart Malformations 61 3.220
11
ART111 Artery Disease 56 0.530
12
P CRN211 Coronary Artery Disease 74 0.482
13
ANR040 Aneurysm 56 0.449
14
P VNT002 Ventricular Septal Defect 59 0.419
15
CRB009 Cerebritis 36 0.407
16
c CNG401 Congenital Heart Disease 67 0.351
17
P MYC007 Myocardial Infarction 80 0.342
18
P HRT032 Heart Disease 64 0.330
19
ISC004 Ischemia 56 0.314
20
P PLM037 Pulmonary Hypertension 78 0.307
21
ATH003 Atherosclerosis 63 0.274
22
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.272
23
DXT001 Dextrocardia 44 0.263
24
ISC006 Ischemic Heart Disease 54 0.248
25
P CRV039 Cervicitis 45 0.246
26
STS002 Situs Inversus 43 0.236
27
P LKM002 Leukemia 70 0.231
28
TRC062 Tricuspid Atresia 34 0.230
29
P NRP001 Neuropathy 57 0.229
30
c ACT075 Acute Myocardial Infarction 61 0.227
31
P LYM118 Lymphoma 68 0.223
32
P ADN016 Adenocarcinoma 69 0.219
33
TTR001 Tetralogy of Fallot 69 0.215
34
P ENC018 Encephalopathy 59 0.214
35
P ART022 Arthritis 73 0.212
36
P TRC086 Trichohepatoenteric Syndrome 1 46 0.211
37
P PNC044 Pancreatitis 62 0.205
38
HYP266 Hypoxia 55 0.202
39
VND001 Vein Disease 51 0.195
40
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.193
41
P OBS005 Obesity 91 0.193
42
ART016 Aortic Aneurysm 67 0.192
43
c CRN172 Coronary Heart Disease 3 19 0.191
44
CRN030 Coronary Stenosis 50 0.187
45
ALR002 Al-Raqad Syndrome 36 0.185
46
P CRD011 Cardiomyopathy 66 0.183
47
MLN008 Melanoma 61 0.182
48
P ESP024 Esophagitis 62 0.178
49
RGH006 Right Aortic Arch 25 0.175
50
P ART034 Aortopulmonary Window 23 0.174
51
CNG034 Congestive Heart Failure 72 0.174
52
P ATR011 Atrial Fibrillation 63 0.173
53
BRN071 Brain Injury 51 0.168
54
TRN012 Transient Global Amnesia 38 0.163
55
ART031 Aortic Coarctation 42 0.163
56
CRT028 Cor Triatriatum 22 0.157
57
P HYP055 Hypoplastic Left Heart Syndrome 60 0.155
58
DMN002 Dementia 62 0.152
59
MDS022 Mediastinitis 37 0.148
60
ATR060 Atrial Standstill, Digenic 51 0.148
61
VSC047 Vascular Malformation 45 0.146
62
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.143
63
PTN001 Patent Foramen Ovale 55 0.142
64
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.140
65
VGN023 Vaginitis 41 0.140
66
P ATR001 Atrioventricular Septal Defect 52 0.139
67
SDD007 Sudden Cardiac Death 46 0.137
68
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.136
69
SNG003 Single Ventricular Heart 23 0.136
70
P HYD006 Hydrocephalus 68 0.135
71
SBC014 Subclavian Steal Syndrome 30 0.135
72
P END033 Endocarditis 52 0.135
73
ATR057 Atrioventricular Block 49 0.135
74
PLM070 Pulmonic Stenosis 59 0.134
75
P THR014 Thrombocytopenia 63 0.133
76
CRD119 Cardiac Arrest 63 0.131
77
KDS001 Kid Syndrome 53 0.130
78
ART017 Aortic Disease 57 0.130
79
CRS011 Criss-Cross Heart 20 0.129
80
CHL071 Child Syndrome 58 0.129
81
SBP005 Subpulmonary Stenosis 12 0.127
82
DDN006 Duodenitis 44 0.125
83
CRN073 Coronary Arteries Congenital Malformation 11 0.122
84
WLF001 Wolff-Parkinson-White Syndrome 58 0.120
85
P CNG015 Congenital Diaphragmatic Hernia 58 0.119
86
CSY001 C Syndrome 49 0.118
87
P PLM064 Pulmonary Sequestration 26 0.117
88
CMP035 Complete Atrioventricular Canal 29 0.117
89
P TBR001 Tuberous Sclerosis 68 0.116
90
CHR008 Choroiditis 43 0.115
91
ART005 Arteriovenous Malformation 63 0.115
92
LPM004 Lipoma 59 0.109
93
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.109
94
P ALZ034 Alzheimer Disease 92 0.109
95
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.108
96
PTN002 Patent Ductus Arteriosus 50 0.107
97
KRT002 Keratomalacia 50 0.107
98
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.106
99
EBS001 Ebstein Anomaly 44 0.104
100
IMP002 Imperforate Anus 54 0.104
101
BCK006 Back Pain 40 0.103
102
P CRD013 Cardiofaciocutaneous Syndrome 65 0.101
103
SPN331 Spondyloocular Syndrome 27 0.097
104
MTR027 Mitral Atresia 15 0.097
105
VHW001 Vohwinkel Syndrome 47 0.095
106
END020 Endocardial Fibroelastosis 44 0.095
107
P SCK002 Sick Sinus Syndrome 49 0.094
108
P LMY004 Leiomyosarcoma 54 0.094
109
c MLT114 Multiple Ventricular Septal Defects 16 0.094
110
PLM068 Pulmonary Vein Stenosis 39 0.093
111
P TRC087 Tricuspid Valve Disease 41 0.093
112
P ATR010 Atrial Heart Septal Defect 41 0.093
113
P CMM008 Communicating Hydrocephalus 31 0.093
114
P KLP003 Klippel-Feil Syndrome 47 0.093
115
BLR001 Biliary Atresia 52 0.092
116
UNV002 Univentricular Heart 24 0.092
117
PLM059 Pulmonary Atresia with Ventricular Septal Defect 19 0.092
118
PLM116 Pulmonary Artery Hypoplasia 16 0.091
119
MSC086 Mesocardia 12 0.090
120
c TRC022 Tricuspid Valve Insufficiency 33 0.090
121
HRT012 Heart Valve Disease 39 0.090
122
TWN001 Twin-to-Twin Transfusion Syndrome 47 0.089
123
P GST044 Gastritis 64 0.089
124
OMP004 Omphalocele 51 0.087
125
NSL022 Nasal Cavity Disease 41 0.087
126
BRN024 Bronchitis 67 0.086
127
OST017 Osteomyelitis 60 0.086
128
GLC011 Galactose Epimerase Deficiency 39 0.086
129
PRN021 Paranasal Sinus Disease 50 0.086
130
CRB037 Cerebral Palsy 54 0.085
131
DST006 Diastolic Heart Failure 45 0.084
132
CRT060 Cor Triatriatum Sinister 19 0.084
133
PLG002 Plague 49 0.083
134
ACC011 Accessory Mitral Valve Tissue 14 0.082
135
DBL004 Double Discordia 9 0.081
136
CYN002 Cyanosis, Transient Neonatal 29 0.080
137
ESN011 Eisenmenger Syndrome 45 0.080
138
SCL046 Scalp-Ear-Nipple Syndrome 30 0.079
139
STR029 Sternal Cleft 19 0.078
140
INT060 Intestinal Atresia 37 0.078
141
AZY001 Azygos Continuation of the Inferior Vena Cava 15 0.078
142
ART095 Aortic Valve Atresia 11 0.077
143
P CTR001 Citrullinemia 60 0.077
144
TRC037 Tracheobronchomalacia 20 0.077
145
MYC005 Myocardial Stunning 44 0.075
146
FCL064 Facial Dysmorphism with Multiple Malformations 25 0.074
147
CDL003 Caudal Regression Syndrome 52 0.072
148
P HLP001 Holoprosencephaly 62 0.072
149
FTL007 Fetal Hydantoin Syndrome 28 0.070
150
OSC001 Oeis Complex 27 0.070
151
P CRC039 Coarctation of Aorta 32 0.069
152
NTH001 Netherton Syndrome 52 0.069
153
SPR035 Superior Vena Cava Syndrome 31 0.068
154
JXT004 Juxtaposition of the Atrial Appendages 9 0.067
155
PLM108 Pulmonary Interstitial Glycogenosis 15 0.067
156
PRX085 Preaxial Hallucal Polydactyly 18 0.067
157
JCK001 Jackson-Weiss Syndrome 50 0.064
158
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.064
159
KMM002 Kommerell Diverticulum 15 0.064
160
CHR266 Chromosome 8p23.1 Deletion 20 0.063
161
NRC019 Neurocutaneous Melanosis, Somatic 38 0.063
162
c BNG076 Benign Exophthalmos Syndrome 15 0.063
163
RGH009 Right Atrial Isomerism 31 0.061
164
HTR014 Heterotaxy, Visceral, 1, X-Linked 31 0.061
165
P CRN015 Cornelia De Lange Syndrome 65 0.061
166
ALD010 Aldosteronism, Glucocorticoid-Remediable 48 0.060
167
EXS016 Exstrophy of Bladder Bladder Exstrophy and Epispadias Complex, Included 26 0.059
168
CHM006 Chime Syndrome 32 0.059
169
KLN001 Klinefelter's Syndrome 52 0.058
170
DBL007 Double Outlet Left Ventricle 18 0.058
171
EPD065 Epidermolytic Ichthyosis 38 0.058
172
CHR539 Chromosome 22q11.2 Microduplication Syndrome 33 0.057
173
OMP007 Omphalocele, Exstrophy of the Cloaca, Imperforate Anus, and Spinal Defects Complex 13 0.057
174
PRS111 Persistent Fifth Aortic Arch 14 0.057
175
RGH003 Right Ventricle Hypoplasia 12 0.056
176
FTL058 Fetal Trimethadione Syndrome 13 0.055
177
VTR016 Vater/vacterl Association 37 0.055
178
c HTR013 Heterotaxy, Visceral, 6, Autosomal Recessive 19 0.055
179
16P004 16p13.11 Microduplication Syndrome 9 0.055
180
DXT002 Dextrocardia with Situs Inversus 34 0.053
181
c HTR008 Heterotaxy, Visceral, 5 26 0.053
182
P HRT035 Heart Block, Congenital 40 0.051
183
THR017 Thoracoabdominal Syndrome 26 0.048
184
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 38 0.048
185
P CRP007 Carpenter Syndrome 49 0.047
186
PLS031 Plastic Bronchitis 22 0.046
187
GNT043 Genitopalatocardiac Syndrome 17 0.045
188
DBL010 Double-Orifice Mitral Valve 16 0.045
189
c CRN139 Cornelia De Lange Syndrome 1 37 0.044
190
CNG108 Congenital Mitral Stenosis 16 0.044
191
c CRP022 Carpenter Syndrome 2 30 0.043
192
PNC092 Pancreatic Agenesis and Congenital Heart Defects 27 0.043
193
SHR064 Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly 27 0.042
194
c CRN135 Cornelia De Lange Syndrome 3 25 0.042
195
KLL013 Kallmann Syndrome-Heart Disease Syndrome 9 0.042
196
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 45 0.041
197
CHR583 Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb 15 0.041
198
NLX002 Neu-Laxova Syndrome1 35 0.040
199
MCH011 Meacham Syndrome 27 0.040
200
PLY133 Polysyndactyly with Cardiac Malformation 13 0.039
201
c CNG404 Congenital Heart Defects, Multiple Types, 4 27 0.039
202
CRB080 Cor Biloculare 8 0.039
203
MD1002 Med13l Syndrome 11 0.038