Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
R-numbers: R15 Signed-off version 6.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Heme oxygenase-1 deficiency, OMIM:614034, Hemolysis, nephritis, inflammation, Defects in Intrinsic and Innate Immunity, amyloidosis |