C4orf26

odontogenesis associated phosphoprotein
OMIM: 614829
PanelMode of inheritanceDetails
2 panels
R-numbers: R340
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Amelogenesis imperfecta, type IIA4, 614832, Amelogenesis Imperfecta, Type IIA4, 614832, hypomineralized amelogenesis imperfecta
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
AMYELOGENESIS 614832