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 Congenital hypothyroidism Beckwith-Wiedemann syndrome Differentiated thyroid carcinoma Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Prader-Willi syndrome Silver-Russell syndrome Medullary thyroid carcinoma Carney complex