neonatal respiratory distress Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Respiratory difficulty as newborn. (Human Phenotype Ontology, HP_0002643)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002643
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Genes

10 genes associated with the neonatal respiratory distress phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALDH7A1 aldehyde dehydrogenase 7 family, member A1
CHRNG cholinergic receptor, nicotinic, gamma (muscle)
CUL7 cullin 7
MTM1 myotubularin 1
NKX2-1 NK2 homeobox 1
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
PLEC plectin
RUNX2 runt-related transcription factor 2
SBDS Shwachman-Bodian-Diamond syndrome
ZC4H2 zinc finger, C4H2 domain containing