Catalog

Primary congenital hypothyroidism due to a developmental anomaly

No MMS code

Link to WHO Definition

Primary congenital hypothyroidism due to a developmental anomaly – http://id.who.int/icd/entity/317417941

Thyroid dysgenesis is a type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth, and occurs in three major forms: thyroid ectopy, athyreosis and thyroid hypoplasia.