Catalog

Congenital hypothyroidism due to thyroglobulin mutations

No MMS code

Link to WHO Definition

Congenital hypothyroidism due to thyroglobulin mutations – http://id.who.int/icd/entity/457788707

This is a congenital state in which the thyroid gland does not make enough thyroid hormone. This diagnosis is due to thyroglobulin mutations.

Parents

Primary congenital hypothyroidism due to impaired hormone production