SE-ATLAS

Rare genetic thyroid disease Pituitary deficiency Chronic primary adrenal insufficiency Genetic obesity Noonan syndrome Familial hyperaldosteronism Pituitary adenoma Rare hypothyroidism Rare hyperthyroidism Adrenocortical carcinoma Congenital adrenal hyperplasia ACTH-independent Cushing syndrome due to rare cortisol-producing adrenal tumor Familial hyperthyroidism due to mutations in TSH receptor Hereditary pheochromocytoma-paraganglioma Acquired pituitary hormone deficiency Hypothyreose, kongenitale Beckwith-Wiedemann-Syndrom Schilddrüsenkarzinom, differenziertes Schilddrüsenkarzinom, medulläres Carney-Komplex Neoplasie, endokrine multiple, Typ 1 Neoplasie, endokrine multiple, Typ 2 Silver-Russell-Syndrom