Catalog

Primary congenital hypothyroidism due to TSH receptor mutations

No MMS code

Link to WHO Definition

Primary congenital hypothyroidism due to TSH receptor mutations – http://id.who.int/icd/entity/639660415

A type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth due to thyroid resistance to TSH (Thyroid-stimulating hormone).