ALB

PanelMode of inheritanceDetails
1 panel
R-numbers: R182
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial dysalbuminaemic hyperthyroxinaemia, [Dysalbuminemic hyperthyroxinemia], OMIM:615999, ?[Dysalbuminemic hypertriiodothyroninemia], OMIM:615999