Disease: Meningomyelocele ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		0.310 GeneticVariation disease BEFREE These results may suggest that polymorphisms in ALDH1A2 may influence the risk for lumbosacral myelomeningocele in humans. 16237707 2005
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		0.310 GeneticVariation disease LHGDN These results may suggest that polymorphisms in ALDH1A2 may influence the risk for lumbosacral myelomeningocele in humans. 16237707 2005
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele 		0.310 Biomarker disease CTD_human These results may suggest that polymorphisms in ALDH1A2 may influence the risk for lumbosacral myelomeningocele in humans. 16237707 2005