Search results for nkx2-5

52 hits were found for nkx2-5

# Family MCID Name MIFTS Score
1
TTR001 Tetralogy of Fallot 71 5.705
2
P HRT032 Heart Disease 75 5.371
3
ATR063 Atrial Septal Defect 7, with or Without Av Conduction Defects 26 5.008
4
c VNT024 Ventricular Septal Defect 3 25 4.587
5
P CNT061 Conotruncal Heart Malformations 62 4.512
6
P VNT002 Ventricular Septal Defect 60 4.213
7
c HYP354 Hypothyroidism, Congenital Nongoitrous, 5 20 4.213
8
P HYP055 Hypoplastic Left Heart Syndrome 61 4.148
9
PTN001 Patent Foramen Ovale 55 4.148
10
P HYP086 Hypothyroidism 64 4.071
11
c HYP517 Hypoplastic Left Heart Syndrome 2 25 3.773
12
c FML001 Familial Atrial Fibrillation 58 3.746
13
c CNG006 Congenital Hypothyroidism 60 3.716
14
ATR057 Atrioventricular Block 49 3.716
15
PYL006 Pyloric Stenosis 46 3.387
16
P HYP009 Hypertrophic Pyloric Stenosis 42 3.387
17
P HLT001 Holt-Oram Syndrome 61 3.324
18
P ATR001 Atrioventricular Septal Defect 52 3.324
19
P ATR010 Atrial Heart Septal Defect 45 3.324
20
EBS001 Ebstein Anomaly 45 3.324
21
HRT011 Heart Septal Defect 40 3.324
22
c DLT002 Dilated Cardiomyopathy 76 2.916
23
ATH010 Athyreosis 31 2.916
24
c FML250 Familial Progressive Cardiac Conduction Defect 28 2.916
25
THY098 Thyroid Ectopia 25 2.916
26
ASP026 Asplenia, Isolated Congenital 24 2.916
27
DLT013 Deletion 5q35 13 2.916
28
WLF001 Wolff-Parkinson-White Syndrome 56 2.878
29
TRN044 Transposition of the Great Arteries 48 2.878
30
P TRC087 Tricuspid Valve Disease 44 2.878
31
OVR051 Ovarian Endodermal Sinus Tumor 34 2.878
32
CHR581 Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb 31 2.878
33
OVR056 Ovarian Primitive Germ Cell Tumor 28 2.878
34
c CRD099 Cardiomyopathy, Dilated, 1e 52 2.350
35
CHR101 Char Syndrome 49 2.350
36
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 44 2.350
37
TRC062 Tricuspid Atresia 43 2.350
38
P CRD132 Cardiac Conduction Defect 43 2.350
39
CHR554 Chromosome 17q11.2 Deletion Syndrome 13 2.350
40
P LKM002 Leukemia 71 0.140
41
P LYM026 Lymphoblastic Leukemia 62 0.140
42
P CRD011 Cardiomyopathy 68 0.122
43
P ATR011 Atrial Fibrillation 66 0.099
44
P THY032 Thyroiditis 54 0.099
45
INT276 Interatrial Communication 20 0.099
46
DWN001 Down Syndrome 66 0.070
47
P MSC005 Muscular Dystrophy 65 0.070
48
WLF002 Wolf-Hirschhorn Syndrome 49 0.070
49
SDD007 Sudden Cardiac Death 47 0.070
50
P HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 36 0.070
51
c VNT028 Ventricular Septal Defect 1 27 0.070
52
c HYP543 Hypoplastic Left Heart Syndrome 1 20 0.070
Content
Loading form....