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"

211 hits were found for 'transposition of great arteries'

# Family MCID Name MIFTS Score
1
CNG134 Congenitally Corrected Transposition of the Great Arteries 24 8.092
2
TRN044 Transposition of the Great Arteries 48 7.836
3
c TRN035 Transposition of Great Arteries, Dextro-Looped 3 19 7.026
4
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 29 6.980
5
P DXT004 Dextro-Looped Transposition of the Great Arteries 34 6.850
6
c TRN036 Transposition of the Great Arteries, Dextro-Looped 2 12 4.616
7
CNG259 Congenitally Uncorrected Transposition of the Great Arteries with Cardiac Malformation 5 3.518
8
CNG359 Congenitally Uncorrected Transposition of the Great Arteries with Coarctation 5 3.518
9
ISL054 Isolated Congenitally Uncorrected Transposition of the Great Arteries 5 3.518
10
P CNT061 Conotruncal Heart Malformations 62 3.190
11
ART111 Artery Disease 55 0.518
12
P CRN211 Coronary Artery Disease 74 0.458
13
ANR040 Aneurysm 57 0.425
14
P VNT002 Ventricular Septal Defect 60 0.404
15
CRB009 Cerebritis 39 0.389
16
P HRT032 Heart Disease 75 0.343
17
P MYC007 Myocardial Infarction 79 0.325
18
ISC004 Ischemia 61 0.311
19
THR024 Thrombosis 57 0.305
20
P PLM037 Pulmonary Hypertension 79 0.299
21
LFT009 Left Ventricular Outflow Tract Obstruction 43 0.271
22
ATH003 Atherosclerosis 65 0.269
23
DXT001 Dextrocardia 43 0.252
24
ISC006 Ischemic Heart Disease 68 0.242
25
P CRV039 Cervicitis 45 0.239
26
P BRS047 Breast Cancer 100 0.234
27
P LKM002 Leukemia 71 0.233
28
STS002 Situs Inversus 46 0.231
29
TRC062 Tricuspid Atresia 43 0.225
30
P NRP001 Neuropathy 59 0.224
31
P ADN016 Adenocarcinoma 69 0.220
32
P LYM118 Lymphoma 69 0.220
33
P ART022 Arthritis 75 0.211
34
c ACT075 Acute Myocardial Infarction 60 0.209
35
TTR001 Tetralogy of Fallot 71 0.205
36
P PNC044 Pancreatitis 61 0.203
37
P ENC018 Encephalopathy 59 0.196
38
VND001 Vein Disease 47 0.190
39
P OBS005 Obesity 92 0.190
40
HYP266 Hypoxia 56 0.189
41
c CRN172 Coronary Heart Disease 3 19 0.185
42
MLN008 Melanoma 62 0.182
43
ART016 Aortic Aneurysm 69 0.178
44
P ESP024 Esophagitis 61 0.178
45
P CRD011 Cardiomyopathy 68 0.174
46
CRN030 Coronary Stenosis 51 0.173
47
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.173
48
CNG034 Congestive Heart Failure 72 0.172
49
SQM006 Squamous Cell Carcinoma 70 0.168
50
RGH006 Right Aortic Arch 27 0.165
51
P ART034 Aortopulmonary Window 23 0.164
52
P ATR011 Atrial Fibrillation 66 0.162
53
BRN071 Brain Injury 52 0.159
54
P TRC086 Trichohepatoenteric Syndrome 1 48 0.158
55
VSC047 Vascular Malformation 45 0.150
56
DMN002 Dementia 65 0.150
57
ALR002 Al-Raqad Syndrome 36 0.148
58
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.148
59
ATR060 Atrial Standstill, Digenic 51 0.148
60
P HYP055 Hypoplastic Left Heart Syndrome 61 0.146
61
ART031 Aortic Coarctation 43 0.145
62
MDS022 Mediastinitis 41 0.144
63
CRT028 Cor Triatriatum 22 0.144
64
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.140
65
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.138
66
SKN023 Skin Tag 44 0.133
67
KDS001 Kid Syndrome 53 0.131
68
CHL071 Child Syndrome 58 0.131
69
ART017 Aortic Disease 57 0.128
70
TRN012 Transient Global Amnesia 39 0.127
71
CRN073 Coronary Arteries Congenital Malformation 10 0.127
72
SNG003 Single Ventricular Heart 22 0.126
73
PLM070 Pulmonic Stenosis 59 0.125
74
P ATR001 Atrioventricular Septal Defect 52 0.125
75
PTN001 Patent Foramen Ovale 55 0.125
76
P HYD006 Hydrocephalus 66 0.125
77
SBC014 Subclavian Steal Syndrome 28 0.123
78
SDD007 Sudden Cardiac Death 47 0.123
79
DDN006 Duodenitis 42 0.122
80
VGN023 Vaginitis 42 0.122
81
CSY001 C Syndrome 50 0.121
82
P THR014 Thrombocytopenia 64 0.121
83
ATR057 Atrioventricular Block 49 0.121
84
P END033 Endocarditis 54 0.120
85
CRD119 Cardiac Arrest 61 0.119
86
SBP005 Subpulmonary Stenosis 12 0.119
87
CRS011 Criss-Cross Heart 19 0.116
88
ART005 Arteriovenous Malformation 66 0.111
89
CHR008 Choroiditis 44 0.111
90
P CNG015 Congenital Diaphragmatic Hernia 60 0.109
91
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.109
92
P ALZ034 Alzheimer Disease 92 0.107
93
P PTN002 Patent Ductus Arteriosus 52 0.106
94
P TBR001 Tuberous Sclerosis 67 0.106
95
P PLM064 Pulmonary Sequestration 27 0.104
96
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.104
97
WLF001 Wolff-Parkinson-White Syndrome 56 0.103
98
LPM004 Lipoma 60 0.102
99
BCK006 Back Pain 43 0.102
100
CMP035 Complete Atrioventricular Canal 36 0.101
101
P LMY004 Leiomyosarcoma 55 0.094
102
HRT012 Heart Valve Disease 40 0.091
103
PLM059 Pulmonary Atresia with Ventricular Septal Defect 22 0.090
104
IMP002 Imperforate Anus 52 0.090
105
OST017 Osteomyelitis 61 0.087
106
MTR027 Mitral Atresia 17 0.087
107
EBS001 Ebstein Anomaly 45 0.087
108
KRT002 Keratomalacia 52 0.087
109
NSL022 Nasal Cavity Disease 38 0.087
110
PRN021 Paranasal Sinus Disease 49 0.086
111
CRB037 Cerebral Palsy 66 0.085
112
PLM068 Pulmonary Vein Stenosis 40 0.084
113
BRN024 Bronchitis 64 0.083
114
END020 Endocardial Fibroelastosis 44 0.083
115
PLG002 Plague 51 0.083
116
P CRD013 Cardiofaciocutaneous Syndrome 63 0.083
117
P CMM008 Communicating Hydrocephalus 36 0.082
118
P GST044 Gastritis 56 0.082
119
UNV002 Univentricular Heart 26 0.082
120
DST006 Diastolic Heart Failure 46 0.081
121
P SCK002 Sick Sinus Syndrome 50 0.081
122
BLR001 Biliary Atresia 52 0.080
123
P KLP003 Klippel-Feil Syndrome 46 0.080
124
PLM116 Pulmonary Artery Hypoplasia 17 0.079
125
ESN011 Eisenmenger Syndrome 45 0.078
126
RGH009 Right Atrial Isomerism 44 0.077
127
TWN001 Twin-to-Twin Transfusion Syndrome 48 0.076
128
P TRC087 Tricuspid Valve Disease 44 0.075
129
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.075
130
OMP004 Omphalocele 50 0.075
131
CRT060 Cor Triatriatum Sinister 18 0.073
132
PNC092 Pancreatic Agenesis and Congenital Heart Defects 30 0.073
133
MSC086 Mesocardia 12 0.072
134
P HLP001 Holoprosencephaly 63 0.071
135
HTR014 Heterotaxy, Visceral, 1, X-Linked 36 0.071
136
MYC005 Myocardial Stunning 44 0.071
137
ACC011 Accessory Mitral Valve Tissue 13 0.070
138
c TRC022 Tricuspid Valve Insufficiency 33 0.070
139
P CRC039 Coarctation of Aorta 34 0.069
140
HPT074 Hepatic Adenoma, Somatic 50 0.068
141
SPN331 Spondyloocular Syndrome 27 0.068
142
AZY001 Azygos Continuation of the Inferior Vena Cava 14 0.066
143
ART095 Aortic Valve Atresia 13 0.066
144
SPR035 Superior Vena Cava Syndrome 31 0.066
145
PRX085 Preaxial Hallucal Polydactyly 18 0.065
146
INT060 Intestinal Atresia 42 0.065
147
TRC037 Tracheobronchomalacia 23 0.065
148
P CTR001 Citrullinemia 59 0.064
149
HNM002 Hinman Syndrome 25 0.064
150
STR029 Sternal Cleft 18 0.064
151
KMM002 Kommerell Diverticulum 14 0.063
152
FCL064 Facial Dysmorphism with Multiple Malformations 23 0.062
153
CHR266 Chromosome 8p23.1 Deletion 19 0.062
154
CHL127 Cholangiocarcinoma, Susceptibility to 54 0.062
155
GLC011 Galactose Epimerase Deficiency 41 0.061
156
BLD130 Bladder Exstrophy 42 0.061
157
P CRN015 Cornelia De Lange Syndrome 62 0.060
158
DBL004 Double Discordia 8 0.059
159
KLN001 Klinefelter's Syndrome 50 0.059
160
FTL007 Fetal Hydantoin Syndrome 32 0.058
161
DBL007 Double Outlet Left Ventricle 19 0.057
162
CYN002 Cyanosis, Transient Neonatal 28 0.057
163
OSC001 Oeis Complex 26 0.057
164
SCL046 Scalp-Ear-Nipple Syndrome 29 0.056
165
CHR539 Chromosome 22q11.2 Microduplication Syndrome 31 0.056
166
P ATX010 Ataxia Neuropathy Spectrum 30 0.056
167
PRS111 Persistent Fifth Aortic Arch 14 0.056
168
P SYN001 Syndactyly 53 0.055
169
JXT004 Juxtaposition of the Atrial Appendages 9 0.055
170
VTR016 Vater/vacterl Association 46 0.054
171
PLM108 Pulmonary Interstitial Glycogenosis 14 0.054
172
P HRT035 Heart Block, Congenital 38 0.054
173
FTL058 Fetal Trimethadione Syndrome 13 0.054
174
c HTR013 Heterotaxy, Visceral, 6, Autosomal Recessive 19 0.054
175
16P004 16p13.11 Microduplication Syndrome 10 0.053
176
c HTR008 Heterotaxy, Visceral, 5 38 0.052
177
NTH001 Netherton Syndrome 54 0.051
178
JCK001 Jackson-Weiss Syndrome 49 0.051
179
DXT002 Dextrocardia with Situs Inversus 37 0.050
180
P RNL100 Renal Hypodysplasia/aplasia 1 53 0.049
181
P ACQ009 Acquired Metabolic Disease 38 0.049
182
NRC019 Neurocutaneous Melanosis, Somatic 39 0.047
183
P CRP007 Carpenter Syndrome 51 0.047
184
INT276 Interatrial Communication 20 0.046
185
THR017 Thoracoabdominal Syndrome 25 0.046
186
PLS031 Plastic Bronchitis 24 0.046
187
c SMP007 Simpson-Golabi-Behmel Syndrome, Type 1 40 0.046
188
GNT043 Genitopalatocardiac Syndrome 16 0.045
189
DBL010 Double-Orifice Mitral Valve 16 0.044
190
EPD065 Epidermolytic Ichthyosis 37 0.044
191
c CRN139 Cornelia De Lange Syndrome 1 48 0.044
192
EXS016 Exstrophy of Bladder Bladder Exstrophy and Epispadias Complex, Included 25 0.043
193
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 48 0.043
194
CNG108 Congenital Mitral Stenosis 18 0.043
195
c CRP022 Carpenter Syndrome 2 31 0.042
196
CHM006 Chime Syndrome 32 0.042
197
SHR064 Short-Rib Thoracic Dysplasia 10 with or Without Polydactyly 27 0.042
198
c CRN135 Cornelia De Lange Syndrome 3 26 0.042
199
OMP007 Omphalocele, Exstrophy of the Cloaca, Imperforate Anus, and Spinal Defects Complex 11 0.041
200
c BNG076 Benign Exophthalmos Syndrome 15 0.041
201
c CLC039 Celiac Disease 13 18 0.041
202
ALD010 Aldosteronism, Glucocorticoid-Remediable 49 0.040
203
RGH003 Right Ventricle Hypoplasia 11 0.040
204
NLX002 Neu-Laxova Syndrome1 38 0.040
205
CHR583 Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb 15 0.039
206
c CNG404 Congenital Heart Defects, Multiple Types, 4 26 0.039
207
CRB080 Cor Biloculare 9 0.039
208
VCT007 Vacterl Association, X-Linked 20 0.038
209
THK001 Thakker-Donnai Syndrome 9 0.038
210
MD1002 Med13l Syndrome 11 0.038
211
MNT266 Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects 8 0.038