Bronchopulmonary dysplasia Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Bronchopulmonary dysplasia is a chronic respiratory disease that results from complications related to lung injury during the treatment of respiratory distress syndrome in low-birth-weight premature infants or from abnormal lung development in older infants. Clinical signs are tachypnea, tachycardia and signs of respiratory distress such as intercostal recession, grunting and nasal flaring. (Orphanet Rare Disease Ontology, Orphanet_70589)
External Link https://www.ebi.ac.uk/gwas/search?query=Bronchopulmonary dysplasia
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Genes

15 genes associated with the Bronchopulmonary dysplasia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
CTNNA3 catenin (cadherin-associated protein), alpha 3 0.220915
STXBP5 syntaxin binding protein 5 (tomosyn) 0.220915
PAMR1 peptidase domain containing associated with muscle regeneration 1 0.165905
CHST9 carbohydrate (N-acetylgalactosamine 4-0) sulfotransferase 9 0.129504
KLF12 Kruppel-like factor 12 0.129504
GRHL2 grainyhead-like 2 (Drosophila) 0.129504
PLXDC2 plexin domain containing 2 0.129504
FHIT fragile histidine triad 0.129504
CYP2W1 cytochrome P450, family 2, subfamily W, polypeptide 1 0.129504
CEP170 centrosomal protein 170kDa 0.129504
TNK2 tyrosine kinase, non-receptor, 2 0.085234
CARD17 caspase recruitment domain family, member 17 0.085234
LOC100506457 uncharacterized LOC100506457 0.085234
MAGI2 membrane associated guanylate kinase, WW and PDZ domain containing 2 0.070053
HIVEP3 human immunodeficiency virus type I enhancer binding protein 3 0.042592