SLC24A4

solute carrier family 24 member 4
OMIM: 609840
PanelMode of inheritanceDetails
2 panels
R-numbers: R340
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
amelogenesis imperfecta (non-syndromic form), Amelogenesis imperfecta, type IIA5, 615887, hypomaturation/hypomineralised amelogenesis imperfecta
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
AMELOGENESIS IMPERFECTA.