SE-ATLAS

22q11.2 deletion syndrome ACTH-dependent Cushing syndrome ACTH-independent Cushing syndrome Acromegaly Acute adrenal insufficiency Addison disease Adrenal Cushing syndrome Adrenal/paraganglial tumor Adrenocortical carcinoma Adrenogenital syndrome Aldosterone-producing adenoma Apparent mineralocorticoid excess Autoimmune hypoparathyroidism Autoimmune polyendocrinopathy Autoimmune polyendocrinopathy type 1 Autoimmune polyendocrinopathy type 2 Autoimmune polyendocrinopathy type 3 Autoimmune polyendocrinopathy type 4 Bilateral massive adrenal hemorrhage Central diabetes insipidus Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Congenital adrenal hyperplasia Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency Congenital hypothyroidism Congenital isolated hyperinsulinism Congenital thyroid malformation without hypothyroidism Corticosteroid-binding globulin deficiency Craniopharyngioma Cushing disease Cushing syndrome Cushing syndrome due to bilateral macronodular adrenocortical disease Cushing syndrome due to ectopic ACTH secretion Differentiated thyroid carcinoma Endogenous Cushing syndrome Familial gestational hyperthyroidism Familial hyperinsulinism Familial hyperthyroidism due to mutations in TSH receptor Familial multinodular goiter Familial papillary thyroid carcinoma with renal papillary neoplasia Fanconi-Bickel syndrome Generalized resistance to thyroid hormone Gitelman syndrome Glycogen storage disease Glycogen storage disease due to acid maltase deficiency Glycogen storage disease due to aldolase A deficiency Glycogen storage disease due to glucose-6-phosphatase deficiency Glycogen storage disease due to glycogen branching enzyme deficiency Glycogen storage disease due to glycogen debranching enzyme deficiency Glycogen storage disease due to liver glycogen phosphorylase deficiency Glycogen storage disease due to muscle glycogen phosphorylase deficiency Glycogen storage disease due to muscle phosphofructokinase deficiency Hereditary central diabetes insipidus Hereditary pheochromocytoma-paraganglioma Kallmann syndrome McCune-Albright syndrome Medullary thyroid carcinoma Multiple endocrine neoplasia Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Multiple endocrine neoplasia type 4 Neonatal adrenoleukodystrophy Neuroendocrine neoplasm Non-acquired pituitary hormone deficiency Overgrowth syndrome Overgrowth/obesity syndrome Parathyroid carcinoma Pituitary adenoma Pituitary deficiency Pituitary deficiency due to Rathke cleft cysts Pituitary deficiency due to empty sella turcica syndrome Pituitary gigantism Pituitary hormone deficiency of meningeal origin Pituitary hormone deficiency of tumoral origin Pituitary resistance to thyroid hormone Primary adrenal insufficiency Prolactinoma Pseudohypoparathyroidism Rare adrenal disease Rare adult hypothyroidism Rare diabetes mellitus Rare diabetes mellitus type 1 Rare diabetes mellitus type 2 Rare disease with adrenal Cushing syndrome as a major feature Rare endocrine growth disease Rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin Rare hyperthyroidism Rare hypoaldosteronism Rare hypoparathyroidism Rare hypothyroidism Rare primary hyperaldosteronism Rare thyroid carcinoma Rare thyroid disease Rare thyroid tumor Short stature due to growth hormone qualitative anomaly Sporadic pheochromocytoma Sporadic pheochromocytoma/secreting paraganglioma Syndromic obesity TSH-secreting pituitary adenoma Thyroid hypoplasia Turner syndrome Waterhouse-Friderichsen syndrome