Search results for nkx2-5

49 hits were found for nkx2-5

# Family MCID Name MIFTS Score
1
TTR001 Tetralogy of Fallot 69 5.758
2
P HRT032 Heart Disease 75 5.435
3
c VNT024 Ventricular Septal Defect 3 26 4.630
4
P CNT061 Conotruncal Heart Malformations 61 4.553
5
ATR063 Atrial Septal Defect 7, with or Without Av Conduction Defects 26 4.410
6
P VNT002 Ventricular Septal Defect 58 4.252
7
P HYP055 Hypoplastic Left Heart Syndrome 56 4.209
8
P HYP086 Hypothyroidism 60 4.107
9
PTN001 Patent Foramen Ovale 54 3.834
10
c HYP517 Hypoplastic Left Heart Syndrome 2 25 3.808
11
c HYP354 Hypothyroidism, Congenital Nongoitrous, 5 21 3.520
12
c FML001 Familial Atrial Fibrillation 54 3.387
13
c CNG006 Congenital Hypothyroidism 60 3.353
14
ATR057 Atrioventricular Block 49 3.353
15
PYL006 Pyloric Stenosis 45 2.976
16
P HYP009 Hypertrophic Pyloric Stenosis 41 2.976
17
P HLT001 Holt-Oram Syndrome 60 2.904
18
P ATR001 Atrioventricular Septal Defect 52 2.904
19
TRN044 Transposition of the Great Arteries 46 2.904
20
EBS001 Ebstein Anomaly 46 2.904
21
P ATR010 Atrial Heart Septal Defect 42 2.904
22
HRT011 Heart Septal Defect 40 2.904
23
c DLT002 Dilated Cardiomyopathy 74 2.455
24
WLF001 Wolff-Parkinson-White Syndrome 55 2.371
25
c CRD099 Cardiomyopathy, Dilated, 1e 53 2.371
26
CHR101 Char Syndrome 50 2.371
27
ARR025 Arrhythmogenic Right Ventricular Dysplasia 5 46 2.371
28
P TRC087 Tricuspid Valve Disease 45 2.371
29
TRC062 Tricuspid Atresia 42 2.371
30
OVR051 Ovarian Endodermal Sinus Tumor 36 2.371
31
CHR581 Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb 34 2.371
32
OVR056 Ovarian Primitive Germ Cell Tumor 31 2.371
33
ATH010 Athyreosis 35 1.736
34
THY098 Thyroid Ectopia 29 1.736
35
c FML250 Familial Progressive Cardiac Conduction Defect 29 1.736
36
ASP026 Asplenia, Isolated Congenital 25 1.736
37
FML264 Familial Bicuspid Aortic Valve 23 1.736
38
DLT013 Deletion 5q35 14 1.736
39
P LKM002 Leukemia 72 0.143
40
P CRD011 Cardiomyopathy 67 0.143
41
P LYM026 Lymphoblastic Leukemia 60 0.143
42
P ATR011 Atrial Fibrillation 65 0.101
43
P THY032 Thyroiditis 53 0.101
44
INT276 Interatrial Communication 19 0.101
45
DWN001 Down Syndrome 69 0.072
46
P MSC005 Muscular Dystrophy 65 0.072
47
WLF002 Wolf-Hirschhorn Syndrome 50 0.072
48
SDD007 Sudden Cardiac Death 45 0.072
49
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 44 0.072
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