SLC39A4

solute carrier family 39 member 4
OMIM: 607059
PanelMode of inheritanceDetails
4 panels
R-numbers: R164
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica, OMIM:201100
R-numbers: R331
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica, OMIM:201100
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica (Disorder of zinc metabolism), Acrodermatitis enteropathica 201100 (Disorder of zinc metabolism)
R-numbers: R332
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Acrodermatitis enteropathica, OMIM:201100