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"

196 hits were found for 'transposition of great arteries'

# Family MCID Name MIFTS Score
1
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 31 9.050
2
CNG134 Congenitally Corrected Transposition of the Great Arteries 23 8.184
3
TRN044 Transposition of the Great Arteries 47 7.937
4
P TRN035 Transposition of Great Arteries, Dextro-Looped 3 19 7.095
5
c TRN036 Transposition of the Great Arteries, Dextro-Looped 2 12 4.661
6
CNG259 Congenitally Uncorrected Transposition of the Great Arteries with Cardiac Malformation 5 3.553
7
CNG359 Congenitally Uncorrected Transposition of the Great Arteries with Coarctation 5 3.553
8
ISL054 Isolated Congenitally Uncorrected Transposition of the Great Arteries 5 3.553
9
P CNT061 Conotruncal Heart Malformations 62 3.221
10
ART111 Artery Disease 57 0.541
11
P CRN211 Coronary Artery Disease 75 0.477
12
ANR040 Aneurysm 57 0.442
13
P VNT002 Ventricular Septal Defect 59 0.414
14
CRB009 Cerebritis 38 0.405
15
P HRT032 Heart Disease 76 0.348
16
P MYC007 Myocardial Infarction 79 0.334
17
ISC004 Ischemia 59 0.316
18
P PLM037 Pulmonary Hypertension 79 0.307
19
LFT009 Left Ventricular Outflow Tract Obstruction 44 0.278
20
ATH003 Atherosclerosis 62 0.278
21
DXT001 Dextrocardia 44 0.259
22
ISC006 Ischemic Heart Disease 68 0.252
23
P CRV039 Cervicitis 44 0.245
24
P LKM002 Leukemia 70 0.235
25
P NRP001 Neuropathy 60 0.229
26
TRC062 Tricuspid Atresia 34 0.228
27
P ADN016 Adenocarcinoma 69 0.224
28
P LYM118 Lymphoma 70 0.223
29
P ART022 Arthritis 75 0.216
30
c ACT075 Acute Myocardial Infarction 60 0.214
31
TTR001 Tetralogy of Fallot 71 0.211
32
P PNC044 Pancreatitis 60 0.207
33
P ENC018 Encephalopathy 59 0.200
34
VND001 Vein Disease 52 0.196
35
P OBS005 Obesity 93 0.193
36
c CRN172 Coronary Heart Disease 3 21 0.193
37
HYP266 Hypoxia 55 0.193
38
ART016 Aortic Aneurysm 67 0.183
39
CRN030 Coronary Stenosis 50 0.178
40
P ESP024 Esophagitis 62 0.178
41
P CRD011 Cardiomyopathy 67 0.178
42
CNG034 Congestive Heart Failure 71 0.175
43
RGH006 Right Aortic Arch 26 0.171
44
P ART034 Aortopulmonary Window 23 0.170
45
P ATR011 Atrial Fibrillation 64 0.165
46
BRN071 Brain Injury 52 0.161
47
P TRC086 Trichohepatoenteric Syndrome 1 46 0.154
48
DMN002 Dementia 64 0.152
49
ART031 Aortic Coarctation 42 0.150
50
P HYP055 Hypoplastic Left Heart Syndrome 60 0.150
51
ATR060 Atrial Standstill, Digenic 53 0.150
52
ALR002 Al-Raqad Syndrome 36 0.149
53
MDS022 Mediastinitis 41 0.149
54
CRT028 Cor Triatriatum 21 0.148
55
VSC047 Vascular Malformation 45 0.147
56
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.145
57
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.144
58
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 45 0.139
59
KDS001 Kid Syndrome 53 0.133
60
CHL071 Child Syndrome 58 0.133
61
ART017 Aortic Disease 58 0.131
62
PLM070 Pulmonic Stenosis 59 0.129
63
SKN023 Skin Tag 46 0.129
64
SNG003 Single Ventricular Heart 24 0.129
65
P ATR001 Atrioventricular Septal Defect 52 0.128
66
SBC014 Subclavian Steal Syndrome 29 0.128
67
PTN001 Patent Foramen Ovale 54 0.128
68
P HYD006 Hydrocephalus 67 0.127
69
SDD007 Sudden Cardiac Death 46 0.126
70
DDN006 Duodenitis 44 0.126
71
TRN012 Transient Global Amnesia 39 0.125
72
VGN023 Vaginitis 42 0.124
73
P END033 Endocarditis 52 0.123
74
CRN073 Coronary Arteries Congenital Malformation 13 0.123
75
ATR057 Atrioventricular Block 49 0.123
76
CRD119 Cardiac Arrest 63 0.122
77
P THR014 Thrombocytopenia 64 0.122
78
SBP005 Subpulmonary Stenosis 12 0.122
79
CSY001 C Syndrome 49 0.120
80
CRS011 Criss-Cross Heart 19 0.119
81
ART005 Arteriovenous Malformation 65 0.115
82
CHR008 Choroiditis 43 0.114
83
P CNG015 Congenital Diaphragmatic Hernia 58 0.112
84
P PTN002 Patent Ductus Arteriosus 52 0.110
85
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.110
86
P PLM064 Pulmonary Sequestration 26 0.108
87
P ALZ034 Alzheimer Disease 93 0.108
88
WLF001 Wolff-Parkinson-White Syndrome 57 0.105
89
LPM004 Lipoma 58 0.104
90
CMP035 Complete Atrioventricular Canal 29 0.103
91
BCK006 Back Pain 42 0.102
92
c HTR008 Heterotaxy, Visceral, 5 48 0.102
93
P LMY004 Leiomyosarcoma 53 0.095
94
PLM059 Pulmonary Atresia with Ventricular Septal Defect 21 0.092
95
HRT012 Heart Valve Disease 41 0.092
96
IMP002 Imperforate Anus 52 0.091
97
MTR027 Mitral Atresia 16 0.090
98
EBS001 Ebstein Anomaly 44 0.089
99
NSL022 Nasal Cavity Disease 42 0.088
100
KRT002 Keratomalacia 54 0.088
101
OST017 Osteomyelitis 59 0.087
102
PRN021 Paranasal Sinus Disease 50 0.087
103
END020 Endocardial Fibroelastosis 44 0.085
104
CRB037 Cerebral Palsy 54 0.085
105
P CMM008 Communicating Hydrocephalus 37 0.084
106
PLG002 Plague 49 0.084
107
PLM068 Pulmonary Vein Stenosis 39 0.083
108
BRN024 Bronchitis 63 0.083
109
P GST044 Gastritis 58 0.083
110
DST006 Diastolic Heart Failure 46 0.083
111
P SCK002 Sick Sinus Syndrome 50 0.083
112
UNV002 Univentricular Heart 26 0.083
113
PLM116 Pulmonary Artery Hypoplasia 18 0.082
114
BLR001 Biliary Atresia 51 0.082
115
P KLP003 Klippel-Feil Syndrome 46 0.081
116
ESN011 Eisenmenger Syndrome 44 0.080
117
TWN001 Twin-to-Twin Transfusion Syndrome 46 0.079
118
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.078
119
OMP004 Omphalocele 50 0.076
120
P TRC087 Tricuspid Valve Disease 44 0.076
121
FCL064 Facial Dysmorphism with Multiple Malformations 26 0.075
122
CRT060 Cor Triatriatum Sinister 17 0.075
123
MSC086 Mesocardia 12 0.074
124
MYC005 Myocardial Stunning 44 0.073
125
CDL003 Caudal Regression Syndrome 51 0.073
126
P HLP001 Holoprosencephaly 62 0.072
127
ACC011 Accessory Mitral Valve Tissue 13 0.072
128
c TRC022 Tricuspid Valve Insufficiency 34 0.071
129
SPN331 Spondyloocular Syndrome 27 0.070
130
P CRC039 Coarctation of Aorta 33 0.069
131
ART095 Aortic Valve Atresia 13 0.068
132
SPR035 Superior Vena Cava Syndrome 32 0.068
133
AZY001 Azygos Continuation of the Inferior Vena Cava 14 0.068
134
PRX085 Preaxial Hallucal Polydactyly 18 0.067
135
INT060 Intestinal Atresia 40 0.067
136
TRC037 Tracheobronchomalacia 22 0.066
137
P CRD013 Cardiofaciocutaneous Syndrome 63 0.066
138
STR029 Sternal Cleft 18 0.066
139
P CTR001 Citrullinemia 60 0.066
140
KMM002 Kommerell Diverticulum 14 0.066
141
CHR266 Chromosome 8p23.1 Deletion 19 0.064
142
GLC011 Galactose Epimerase Deficiency 40 0.063
143
CHL127 Cholangiocarcinoma, Susceptibility to 55 0.063
144
RGH009 Right Atrial Isomerism 32 0.062
145
DBL004 Double Discordia 8 0.061
146
HTR014 Heterotaxy, Visceral, 1, X-Linked 35 0.061
147
CHM006 Chime Syndrome 33 0.059
148
DBL007 Double Outlet Left Ventricle 17 0.059
149
FTL007 Fetal Hydantoin Syndrome 30 0.059
150
OSC001 Oeis Complex 26 0.059
151
KLN001 Klinefelter's Syndrome 55 0.059
152
CYN002 Cyanosis, Transient Neonatal 31 0.058
153
SCL046 Scalp-Ear-Nipple Syndrome 28 0.058
154
CHR539 Chromosome 22q11.2 Microduplication Syndrome 32 0.057
155
PRS111 Persistent Fifth Aortic Arch 14 0.057
156
JXT004 Juxtaposition of the Atrial Appendages 9 0.056
157
VTR016 Vater/vacterl Association 46 0.056
158
PLM108 Pulmonary Interstitial Glycogenosis 14 0.056
159
FTL058 Fetal Trimethadione Syndrome 13 0.056
160
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.055
161
c HTR013 Heterotaxy, Visceral, 6, Autosomal Recessive 18 0.055
162
16P004 16p13.11 Microduplication Syndrome 10 0.055
163
HPT074 Hepatic Adenoma, Somatic 51 0.055
164
P HRT035 Heart Block, Congenital 39 0.053
165
P CRN139 Cornelia De Lange Syndrome 1 60 0.053
166
NTH001 Netherton Syndrome 52 0.052
167
P DNR003 Duane Retraction Syndrome 1 39 0.052
168
JCK001 Jackson-Weiss Syndrome 49 0.051
169
INT276 Interatrial Communication 20 0.050
170
HNM002 Hinman Syndrome 25 0.050
171
P RNL100 Renal Hypodysplasia/aplasia 1 54 0.050
172
P SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 48 0.048
173
NRC019 Neurocutaneous Melanosis, Somatic 39 0.048
174
THR017 Thoracoabdominal Syndrome 27 0.048
175
P CRP007 Carpenter Syndrome 49 0.047
176
PLS031 Plastic Bronchitis 24 0.047
177
GNT043 Genitopalatocardiac Syndrome 16 0.046
178
DBL010 Double-Orifice Mitral Valve 16 0.045
179
EXS016 Exstrophy of Bladder Bladder Exstrophy and Epispadias Complex, Included 25 0.045
180
CNG108 Congenital Mitral Stenosis 18 0.044
181
ALD010 Aldosteronism, Glucocorticoid-Remediable 48 0.044
182
c CRP022 Carpenter Syndrome 2 31 0.043
183
PNC092 Pancreatic Agenesis and Congenital Heart Defects 28 0.043
184
SHR064 Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly 27 0.043
185
EPD065 Epidermolytic Ichthyosis 35 0.042
186
c CRN135 Cornelia De Lange Syndrome 3 25 0.042
187
KLL013 Kallmann Syndrome-Heart Disease Syndrome 9 0.042
188
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 44 0.042
189
NLX002 Neu-Laxova Syndrome1 34 0.041
190
CHR583 Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb 15 0.041
191
RGH003 Right Ventricle Hypoplasia 13 0.041
192
MCH011 Meacham Syndrome 26 0.040
193
c CNG404 Congenital Heart Defects, Multiple Types, 4 29 0.040
194
PLY133 Polysyndactyly with Cardiac Malformation 13 0.040
195
CRB080 Cor Biloculare 8 0.040
196
MNT266 Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects 8 0.039