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
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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