congenital malformation of the left heart Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0045017
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Genes

13 genes associated with the congenital malformation of the left heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCDC22 coiled-coil domain containing 22
DTNA dystrobrevin, alpha
FOXF1 forkhead box F1
GATA4 GATA binding protein 4
GJA1 gap junction protein, alpha 1, 43kDa
KIAA0196 KIAA0196
MKKS McKusick-Kaufman syndrome
NKX2-5 NK2 homeobox 5
NR2F2 nuclear receptor subfamily 2, group F, member 2
NSDHL NAD(P) dependent steroid dehydrogenase-like
TBX1 T-box 1
TBX5 T-box 5
WT1 Wilms tumor 1