|
2271
|
|
|
Family with sequence similarity 98 member C |
- |
|
|
2272
|
|
|
Dpy-19 like C-mannosyltransferase 3 |
- |
|
|
2273
|
|
|
Adrenoceptor alpha 1A |
ADRA1C, ADRA1L1, ALPHA1AAR |
|
|
2274
|
|
|
Tetratricopeptide repeat domain 9B |
- |
|
|
2275
|
|
|
TIR domain containing adaptor molecule 1 |
IIAE6, MyD88-3, PRVTIRB, TICAM-1, TRIF |
|
|
2276
|
|
|
Zinc finger protein 599 |
- |
|
|
2277
|
|
|
Long intergenic non-protein coding RNA 662 |
- |
|
|
2278
|
|
|
Zinc finger protein 98 |
F7175, ZNF739 |
|
|
2279
|
|
|
NK2 homeobox 5 |
CHNG5, CSX, CSX1, HLHS2, NKX2.5, NKX2E, NKX4-1, VSD3 |
Aneurysm of aortic arch, Aortic coarctation, Aortic valve calcification, Aortic valve disease, Aortic valve insufficiency, Aortic valve sclerosis, Atrial fibrillation, Atrial septal defect, Atrial septal defect with atrioventricular conduction defects, Atrioventricular septal defect, Bicuspid aortic valve, Brachydactyly, Bundle branch block, Camptodactyly of fingers, Cardiomyopathy, Ciliopathies, Congenital exomphalos, Hypoplastic aortic arch, Congenital hypothyroidism, Congenital hypothyroidism, nongoitrous, Congenital myotonic dystrophy, Congestive heart failure, Conotruncal heart defect, Cryptorchidism, Deletion 5q36, Developmental delay, Dolichocephaly, Double outlet right ventricle, Dwarfism, Heart septal defects, Hereditary bundle branch system defect, Hypersomnia, Hypertension, Hypoplastic left heart syndrome, Hypothyroidism, Mental retardation, Macroglossia, Mitral valve stenosis, Monosomy 5q35, Myotonic dystrophy, Paroxysmal atrial fibrillation, Patent ductus arteriosus, Patent foramen ovale, Persistent truncus arteriosus, Polydactyly, Progressive cardiac conduction defect, Proptosis, Secundum atrial septal defect, Splenic hypoplasia, Stroke, Tetralogy of fallot, Thyroid agenesis, Thyroid hypoplasia, Transposition of great vessels, Ventricular septal defectView all (40 more) |
|
2280
|
|
|
Zinc finger protein 555 |
- |
|
