Search results for nkx2-5

53 hits were found for nkx2-5

# Family MCID Name MIFTS Score
1
P TTR001 Tetralogy of Fallot 70 5.705
2
P HRT032 Heart Disease 80 5.433
3
ATR088 Atrial Septal Defect 7 with or Without Atrioventricular Conduction Defects 24 5.310
4
c VNT024 Ventricular Septal Defect 3 18 4.611
5
CNT061 Conotruncal Heart Malformations 70 4.536
6
P VNT002 Ventricular Septal Defect 59 4.236
7
P HYP055 Hypoplastic Left Heart Syndrome 63 4.193
8
P HYP086 Hypothyroidism 62 4.094
9
PTN001 Patent Foramen Ovale 58 3.820
10
c HYP517 Hypoplastic Left Heart Syndrome 2 17 3.794
11
c HYP762 Hypothyroidism, Congenital, Nongoitrous, 5 19 3.505
12
c FML001 Familial Atrial Fibrillation 55 3.376
13
c CNG006 Congenital Hypothyroidism 62 3.343
14
ATR057 Atrioventricular Block 52 3.343
15
P ATR010 Atrial Heart Septal Defect 45 3.072
16
PYL006 Pyloric Stenosis 47 2.965
17
P HYP009 Hypertrophic Pyloric Stenosis 45 2.965
18
HLT001 Holt-Oram Syndrome 61 2.895
19
P ATR001 Atrioventricular Septal Defect 56 2.895
20
EBS001 Ebstein Anomaly 52 2.895
21
TRN044 Transposition of the Great Arteries 49 2.895
22
HRT011 Heart Septal Defect 44 2.895
23
P DLT002 Dilated Cardiomyopathy 76 2.445
24
WLF001 Wolff-Parkinson-White Syndrome 57 2.364
25
c CRD099 Cardiomyopathy, Dilated, 1e 53 2.364
26
CHR101 Char Syndrome 51 2.364
27
TRC062 Tricuspid Atresia 47 2.364
28
ARR018 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 42 2.364
29
P TRC087 Tricuspid Valve Disease 41 2.364
30
OVR051 Ovarian Endodermal Sinus Tumor 38 2.364
31
CHR581 Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb 36 2.364
32
OVR056 Ovarian Primitive Germ Cell Tumor 23 2.364
33
ATH010 Athyreosis 37 1.729
34
c FML250 Familial Progressive Cardiac Conduction Defect 33 1.729
35
FML264 Familial Bicuspid Aortic Valve 30 1.729
36
ASP026 Asplenia, Isolated Congenital 29 1.729
37
THY098 Thyroid Ectopia 25 1.729
38
DLT013 Deletion 5q35 14 1.729
39
P LKM002 Leukemia 75 0.140
40
P LYM026 Lymphoblastic Leukemia 66 0.140
41
c HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 51 0.121
42
P ATR011 Atrial Fibrillation 68 0.099
43
P THY032 Thyroiditis 56 0.099
44
c HYP543 Hypoplastic Left Heart Syndrome 1 38 0.099
45
INT276 Interatrial Communication 22 0.099
46
DWN001 Down Syndrome 70 0.070
47
P MSC005 Muscular Dystrophy 66 0.070
48
c ATR087 Atrial Standstill 1 59 0.070
49
WLF002 Wolf-Hirschhorn Syndrome 54 0.070
50
P CRD132 Cardiac Conduction Defect 53 0.070
51
c CRD233 Cardiomyopathy, Dilated, 1b 51 0.070
52
c MSC050 Muscular Dystrophy, Congenital, 1b 45 0.070
53
c ATR093 Atrial Heart Septal Defect 7 12 0.070
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