| Panel | Mode of inheritance | Details |
|---|---|---|
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 |
Green in HyperthyroidismR-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 |