SLC39A7

solute carrier family 39 member 7
OMIM: 601416
PanelMode of inheritanceDetails
1 panel
R-numbers: R15
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Early onset infections, blistering dermatosis, failure to thrive, thrombocytopenia, Predominantly Antibody Deficiencies, B cell deficiency, Agammaglobulinemia