hypoplastic left heart Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the left side of the heart. May include atresia of the aortic or mitral orifice and hypoplasia of the ascending aorta. (Human Phenotype Ontology, HP_0004383)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004383
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13 genes associated with the hypoplastic 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