chronic lung disease Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description According to the definitions of the American and British Thoracic Societies, including pulmonary functional tests, X-rays, and CT scans for items such as fibrosis, bronchiectasis, bullae, emphysema, nodular or lymphomatous abnormalities. (Human Phenotype Ontology, HP_0006528)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006528
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Genes

5 genes associated with the chronic lung disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BLM Bloom syndrome, RecQ helicase-like
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
PEPD peptidase D
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)