SE-ATLAS

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