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 Kallmann syndrome Glycogen storage disease due to glucose-6-phosphatase deficiency Autoimmune polyendocrinopathy type 4 Rare thyroid disease Multiple endocrine neoplasia Multiple endocrine neoplasia type 4 Sporadic pheochromocytoma Fanconi-Bickel syndrome Rare hyperthyroidism Rare hypothyroidism Rare primary hyperaldosteronism Multiple endocrine neoplasia type 2 Rare diabetes mellitus type 2 Parathyroid carcinoma Familial hyperinsulinism Pituitary resistance to thyroid hormone Multiple endocrine neoplasia type 1 Sporadic pheochromocytoma/secreting paraganglioma Acute adrenal insufficiency Generalized resistance to thyroid hormone Adrenogenital syndrome 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 Rare hypoparathyroidism Cushing syndrome Hereditary pheochromocytoma-paraganglioma Rare thyroid carcinoma Waterhouse-Friderichsen syndrome Familial papillary thyroid carcinoma with renal papillary neoplasia Gitelman syndrome Overgrowth syndrome Autoimmune polyendocrinopathy type 3 Neuroendocrine neoplasm Autoimmune polyendocrinopathy Central diabetes insipidus Pituitary gigantism Rare diabetes mellitus type 1 Overgrowth/obesity syndrome Non-acquired pituitary hormone deficiency Neonatal adrenoleukodystrophy Pituitary deficiency Rare endocrine growth disease Glycogen storage disease Familial gestational hyperthyroidism Thyroid hypoplasia Rare diabetes mellitus Short stature due to growth hormone qualitative anomaly Glycogen storage disease due to muscle glycogen phosphorylase deficiency Autoimmune polyendocrinopathy type 2 Glycogen storage disease due to liver glycogen phosphorylase deficiency Rare adrenal disease Adrenal/paraganglial tumor Glycogen storage disease due to muscle phosphofructokinase deficiency Rare adult hypothyroidism Familial multinodular goiter Familial hyperthyroidism due to mutations in TSH receptor Autoimmune polyendocrinopathy type 1 Congenital adrenal hyperplasia Apparent mineralocorticoid excess Rare thyroid tumor Congenital hypothyroidism Glycogen storage disease due to acid maltase deficiency Primary adrenal insufficiency Glycogen storage disease due to glycogen debranching enzyme deficiency Corticosteroid-binding globulin deficiency Congenital thyroid malformation without hypothyroidism Glycogen storage disease due to glycogen branching enzyme deficiency Craniopharyngioma Syndromic obesity Glycogen storage disease due to aldolase A deficiency Turner syndrome