Preferred Label : Primary congenital hypothyroidism due to a developmental anomaly;
ICD-11 definition : 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.;
ICD-11 synonym : Thyroid dysgenesis; Hypoparathyroidism due to agenesis or dysgenesis of the parathyroid gland;
Origin ID : 317417941;
Automatic exact mappings (from CISMeF team)
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.
