ALB

PanelMode of inheritanceDetails
2 panels
R-numbers: R329
Signed-off version 1.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
[Dysalbuminemic hyperthyroxinemia], OMIM:615999, hyperthyroxinemia, familial dysalbuminemic, MONDO:0014448
R-numbers: R182
Signed-off version 3.7
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Familial dysalbuminaemic hyperthyroxinaemia, [Dysalbuminemic hyperthyroxinemia], OMIM:615999, ?[Dysalbuminemic hypertriiodothyroninemia], OMIM:615999