SLC39A4

solute carrier family 39 member 4
OMIM: 607059
PanelMode of inheritanceDetails
3 panels
R-numbers: R164
Signed-off version 1.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R98
Signed-off version 2.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica (Disorder of zinc metabolism), Acrodermatitis enteropathica 201100 (Disorder of zinc metabolism)
R-numbers: R332
Signed-off version 1.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica, ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE, AEZ