SLC24A4

solute carrier family 24 member 4
OMIM: 609840
PanelMode of inheritanceDetails
1 panel
R-numbers: R340
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
amelogenesis imperfecta (non-syndromic form), Amelogenesis imperfecta, type IIA5, 615887, hypomaturation/hypomineralised amelogenesis imperfecta