Genomics England
GMS Panels
Panels
Genes and Entities

SLC26A7

solute carrier family 26 member 7
OMIM: 608479
PanelMode of inheritanceDetails
1 panel
Green
in Congenital hypothyroidism
R-numbers: R145
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Primary congenital hypothyroidism (dyshormonogenesis)