The detail information of Hypothyroidism, congenital dyshormonogenic, with goiter
OMIA Basic Information

Possible human homologues (MIM numbers):

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Recessive

Considered a defect: yes

Year key mutation first reported: 2018

Species-specific name: -

Species-specific symbol: CDHG

More detail information can see in

Associated Breeds
There are associated breeds.
Associated Gene
There are no associated genes.
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
2018 SolerArias,E.A.,Castillo,V.A.,Garcia,J.D.,Fyfe,J.C.: :
Congenital dyshormonogenic hypothyroidism with goiter caused by a sodium/iodide symporter (SLC5A5) mutation in a family of Shih-Tzu dogs. Domest Anim Endocrinol 65:1-8, 2018.
Pubmed reference: 29777899 . DOI: 10.1016/j.domaniend.2018.04.005 .