SLC7A4, solute carrier family 7 member 4, 6545

N. diseases: 31; N. variants: 0
Disease: Anterior segment mesenchymal dysgenesis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1862839
Disease: Anterior segment mesenchymal dysgenesis
Anterior segment mesenchymal dysgenesis 		0.010 Biomarker disease BEFREE Thus, on the basis of phenotype and map position, Cat4 may be a mouse model of human ASOD. 9166583 1997