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Search results for
tbx20
89 hits were found for tbx20
#
Family
MCID
Name
MIFTS
Score
1
c
ATR031
Atrial Septal Defect 4
30
40.897
2
INT276
Interatrial Communication
51
22.038
3
c
DLT002
Dilated Cardiomyopathy
78
21.012
4
HYP223
Hypoplastic Right Heart Syndrome
32
20.510
5
PTN001
Patent Foramen Ovale
62
20.330
6
P
HYP055
Hypoplastic Left Heart Syndrome
65
19.344
7
P
HRT032
Heart Disease
81
17.803
8
WLF001
Wolff-Parkinson-White Syndrome
65
16.482
9
P
TTR001
Tetralogy of Fallot
69
16.140
10
c
ART115
Aortic Valve Disease 1
74
13.731
11
HRT011
Heart Septal Defect
49
13.375
12
P
VNT002
Ventricular Septal Defect
58
13.014
13
DBL002
Double Outlet Right Ventricle
57
12.432
14
P
ATR010
Atrial Heart Septal Defect
58
12.387
15
LPP008
Lipoprotein Quantitative Trait Locus
65
9.773
16
c
HYP543
Hypoplastic Left Heart Syndrome 1
46
9.572
17
TRC062
Tricuspid Atresia
55
7.862
18
P
ATR001
Atrioventricular Septal Defect
55
7.862
19
P
PTN014
Patent Ductus Arteriosus 1
59
7.862
20
ULN003
Ulnar-Mammary Syndrome
56
7.583
21
P
ATR066
Atrial Septal Defect 2
42
6.910
22
CHR101
Char Syndrome
53
6.910
23
RGH009
Right Atrial Isomerism
57
6.910
24
P
TRC087
Tricuspid Valve Disease
48
6.910
25
c
ATR034
Atrial Septal Defect 6
29
6.910
26
RSP023
Rasopathy
53
6.910
27
CHR103
Charge Syndrome
66
6.910
28
HLT001
Holt-Oram Syndrome
66
6.910
29
c
HRM007
Hermansky-Pudlak Syndrome 4
46
6.910
30
c
MCR241
Microphthalmia, Syndromic 3
55
6.910
31
EBS001
Ebstein Anomaly
55
6.910
32
VLC001
Velocardiofacial Syndrome
57
6.910
33
DGR001
Digeorge Syndrome
62
6.910
34
JCB001
Jacobsen Syndrome
50
6.910
35
P
LFT003
Left Ventricular Noncompaction
57
6.910
36
P
PLM040
Pulmonary Valve Disease
40
6.910
37
PLM041
Pulmonary Valve Stenosis
50
6.910
38
LTM001
Lutembacher's Syndrome
23
6.910
39
c
ATR087
Atrial Standstill 1
74
5.894
40
CRD132
Cardiac Conduction Defect
60
4.394
41
CNG034
Congestive Heart Failure
69
3.588
42
CNT061
Conotruncal Heart Malformations
66
3.496
43
P
MYC007
Myocardial Infarction
70
3.448
44
LMB062
Limb Ischemia
55
3.088
45
P
LNG028
Long Qt Syndrome
64
2.884
46
BLP046
Blepharophimosis, Ptosis, and Epicanthus Inversus
56
2.405
47
P
RTN008
Retinitis Pigmentosa
80
2.405
48
NRR001
Neuroretinitis
42
2.405
49
BLP004
Blepharophimosis
36
2.405
50
RTN023
Retinitis
46
2.405
51
HLX001
Helix Syndrome
48
2.261
52
HYP066
Hyperglycemia
61
1.708
53
P
MTR012
Mitral Valve Disease
57
1.708
54
DSS032
Disease by Infectious Agent
55
1.166
55
SNG003
Single Ventricular Heart
30
0.952
56
P
ATS364
Autism
69
0.673
57
ATH013
Atherosclerosis Susceptibility
63
0.673
58
c
ORF037
Orofaciodigital Syndrome I
59
0.673
59
CRV035
Cervical Cancer
73
0.673
60
MCR037
Macroglossia
44
0.673
61
PLY150
Polykaryocytosis Inducer
29
0.673
62
P
BCK002
Beckwith-Wiedemann Syndrome
62
0.673
63
P
APL001
Aplastic Anemia
73
0.673
64
P
MGL010
Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a
40
0.673
65
UMB002
Umbilical Hernia
47
0.673
66
NRL016
Neural Tube Defects
81
0.673
67
P
LKM062
Leukemia, Acute Lymphoblastic
69
0.673
68
c
VNT027
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
33
0.673
69
P
SPP010
Suppressor of Tumorigenicity 3
51
0.673
70
P
CNG499
Congenital Anomalies of Kidney and Urinary Tract 2
52
0.673
71
P
NNN008
Noonan Syndrome 1
77
0.673
72
P
CTC001
Catecholaminergic Polymorphic Ventricular Tachycardia
63
0.673
73
ADN012
Adenocarcinoma in Situ
43
0.673
74
P
CRV031
Cervical Adenocarcinoma
48
0.673
75
P
PLM175
Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2
51
0.673
76
P
LNG064
Lung Cancer Susceptibility 3
70
0.673
77
P
ADN016
Adenocarcinoma
63
0.673
78
FCL012
Facial Paralysis
49
0.673
79
c
PSD047
Pseudo-Turner Syndrome
52
0.673
80
P
BRS047
Breast Cancer
98
0.602
81
P
PNC035
Pancreatic Cancer
86
0.602
82
c
GLM047
Glioma Susceptibility 3
33
0.464
83
c
MSM022
Mismatch Repair Cancer Syndrome 1
70
0.464
84
c
GLM025
Glioma Susceptibility 2
30
0.464
85
c
GLM043
Glioma Susceptibility 9
30
0.464
86
P
GLM040
Glioma Susceptibility 1
71
0.464
87
MNN043
Meningioma, Familial
79
0.464
88
P
OLG002
Oligodendroglioma
66
0.464
89
GLM045
Glioma
63
0.464
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