SLIT3, slit guidance ligand 3, 6586

N. diseases: 62; N. variants: 7
Disease: Diaphragmatic Hernia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		0.500 Biomarker phenotype MGD Heparan sulfate deficiency disrupts developmental angiogenesis and causes congenital diaphragmatic hernia. 24355925 2014
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		0.500 Biomarker phenotype CTD_human Genetic factors in congenital diaphragmatic hernia. 17436238 2007
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		0.500 Biomarker phenotype MGD A genetic model for a central (septum transversum) congenital diaphragmatic hernia in mice lacking Slit3. 12702769 2003
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		0.500 Biomarker phenotype MGD Slit3-deficient mice represent a genetic animal model for physiological and pathological studies of congenital diaphragmatic hernia. 14550534 2003