Catalog

Transient congenital hypothyroidism due to monoallelic or biallelic mutations of dual oxidase 2 mutation

No MMS code

Link to WHO Definition

Transient congenital hypothyroidism due to monoallelic or biallelic mutations of dual oxidase 2 mutation – http://id.who.int/icd/entity/1830092908

This is a transient congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to heterozygous mutations of monoallelic or biallelic mutations of dual oxidase 2 mutation [DUOX2]