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-Syndrom Gitelman-Syndrom Phäochromozytom-Paragangliom-Syndrom, hereditäres Hypoparathyreoidismus, seltener Waterhouse-Friderichsen-Syndrom Seltenes Schilddrüsenkarzinom Hypophysenhormon-Mangel, nicht erworbener Glykogenose Typ 12 Großwuchs/Adipositas-Syndrom Großwuchs-Syndrom Adrenoleukodystrophie, neonatale Form Apparenter Mineralocorticoid Exzess Diabetes mellitus, seltener Nebennierenkrankheit, seltene Kraniopharyngeom Hypophysenfunktionsstörung Wachstumsstörung, hormonelle Autoimmun-Polyendokrinopathie Typ 2 Nebenniereninsuffizienz, primäre CBG (Cortisol-bindendes Globulin)-Mangel Polyendokrinopathie, autoimmune Glykogenose Tumor, neuroendokriner Glykogenose Typ 2 Glykogenose Typ 3 Diabetes insipidus, zentraler Glykogenose Typ 4 Glykogenose Typ 5 Glykogenose Typ 6 Glykogenose Typ 7 Kleinwuchs durch qualitative Wachstumshormonanomalien Seltener Diabetes mellitus Typ 1 Autoimmun-Polyendokrinopathie Typ 1 Gigantismus, hypophysärer Autoimmun-Polyendokrinopathie Typ 3 Nebennierenhyperplasie, kongenitale Hyperthyreose durch TSH-Rezeptor-Genmutationen, familiäre Form Familiärer multinodulärer Kropf Hypothyreose, kongenitale Hypothyreose, adulte, seltene Schilddrüsenfehlbildung ohne Hypothyreose, kongenital Schilddrüsenhypoplasie Hyperthyreose, familiäre schwangerschaftsbedingte Adipositas, syndromale Seltener Schilddrüsentumor Tumor, adrenaler/paraganglialer