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 Sporadic pheochromocytoma Multiple endocrine neoplasia type 4 Fanconi-Bickel syndrome Familial hyperinsulinism Pituitary resistance to thyroid hormone Rare diabetes mellitus type 2 Parathyroid carcinoma Rare hyperthyroidism Rare hypothyroidism Rare primary hyperaldosteronism Multiple endocrine neoplasia type 2 Sporadic pheochromocytoma/secreting paraganglioma Multiple endocrine neoplasia type 1 Generalized resistance to thyroid hormone Adrenogenital syndrome Acute adrenal insufficiency Hereditary central diabetes insipidus Pseudohypoparathyroidism Rare disease with adrenal Cushing syndrome as a major feature Cushing syndrome due to ectopic ACTH secretion ACTH-dependent Cushing syndrome Endogenous Cushing syndrome Adrenal Cushing syndrome 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 Bilateral massive adrenal hemorrhage Familial papillary thyroid carcinoma with renal papillary neoplasia Rare hypoparathyroidism Gitelman syndrome Hereditary pheochromocytoma-paraganglioma Cushing syndrome Waterhouse-Friderichsen syndrome Rare thyroid carcinoma Non-acquired pituitary hormone deficiency Neonatal adrenoleukodystrophy Autoimmune polyendocrinopathy type 2 Rare diabetes mellitus type 1 Overgrowth syndrome Apparent mineralocorticoid excess Glycogen storage disease Glycogen storage disease due to acid maltase deficiency Glycogen storage disease due to glycogen debranching enzyme deficiency 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 Pituitary gigantism Congenital adrenal hyperplasia Hyperthyreose durch TSH-Rezeptor-Genmutationen, familiäre Form Hypothyreose, kongenitale Schilddrüsenfehlbildung ohne Hypothyreose, kongenital Schilddrüsenhypoplasie Hyperthyreose, familiäre schwangerschaftsbedingte Diabetes mellitus, seltener Nebennierenkrankheit, seltene Hypophysenfunktionsstörung Wachstumsstörung, hormonelle Nebenniereninsuffizienz, primäre Polyendokrinopathie, autoimmune Kleinwuchs durch qualitative Wachstumshormonanomalien Autoimmun-Polyendokrinopathie Typ 3 Adipositas, syndromale Seltener Schilddrüsentumor Tumor, adrenaler/paraganglialer Großwuchs/Adipositas-Syndrom Neuroendokrine Neoplasie Arginin-Vasopressin-Mangel Familiärer multinodulärer Kropf Hypothyreose, adulte, seltene Glykogenose Typ 12 Hypophysenfunktionsstörung durch Zyste der Rathke-Tasche Autoimmun-Polyendokrinopathie Typ 1 CBG (Cortisol-bindendes Globulin)-Mangel