SE-ATLAS

Hypothyroidism due to deficient transcription factors involved in pituitary development or function Peripheral hypothyroidism Congenital hypothyroidism due to maternal intake of antithyroid drugs Genetic transient congenital hypothyroidism X-linked central congenital hypothyroidism with late-onset testicular enlargement Hypothyroidism due to TSH receptor mutations Isolated thyroid-stimulating hormone deficiency Allan-Herndon-Dudley syndrome Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome Isolated thyrotropin-releasing hormone deficiency Neonatal iodine exposure Pituitary resistance to thyroid hormone Transient congenital hypothyroidism due to neonatal factor Transient congenital hypothyroidism due to maternal factor Infantile multisystem neurologic-endocrine-pancreatic disease Peripheral resistance to thyroid hormones Autoimmune polyendocrinopathy type 3 Rare hyperthyroidism Generalized resistance to thyroid hormone Rare hypothyroidism Short stature-delayed bone age due to thyroid hormone metabolism deficiency Pendred syndrome Bamforth-Lazarus syndrome IgG4-related thyroid disease Johanson-Blizzard syndrome Muscular pseudohypertrophy-hypothyroidism syndrome Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Fetal iodine syndrome Transient congenital hypothyroidism Polyendocrine-polyneuropathy syndrome Familial hyperthyroidism due to mutations in TSH receptor Hypothyreose, kongenitale Hypothyreose, adulte, seltene Hypothyreose, syndromale Schilddrüsen-Dysgenesie Athyreose Schilddrüsenektopie Hypothyreose, kongenitale, durch transplazentare Passage von maternalen TSH-bindenden inhibitorischen Antikörpern Hypothyreose, kongenitale primäre, ohne Entwicklungsanomalie der Schilddrüse Hypothyreose, kongenitale, idiopathische Schilddrüsen-Dyshormonogenese, familiäre Schilddrüsenhemiagenesie Blepharophimose-Intelligenzminderung-Syndrom Typ SBBYS Schilddrüsenhypoplasie Hyperthyreose, familiäre schwangerschaftsbedingte Hirn-Lunge-Schilddrüsen-Syndrom Hypothyreose, kongenitale primäre Hypothyreose, kongenitale permanente Hypothyreose, kongenitale zentrale Thyrotropin-Releasing-Hormon (TRH)-Resistenz