SE-ATLAS

Addison disease Adrenocortical carcinoma with pure aldosterone hypersecretion Catecholamine-producing tumor Familial parathyroid adenoma Familial isolated hyperparathyroidism Familial papillary thyroid carcinoma with renal papillary neoplasia Primary hyperaldosteronism-seizures-neurological abnormalities syndrome Familial hyperaldosteronism type III Ectopic aldosterone-producing tumor X-linked adrenoleukodystrophy Hyperparathyroidism-jaw tumor syndrome Autoimmune polyendocrinopathy type 1 Pituitary tumor Neonatal adrenoleukodystrophy Bilateral massive adrenal hemorrhage Rare surgically correctable form of primary aldosteronism Pituitary carcinoma Apparent mineralocorticoid excess Triple A syndrome Rare non surgically correctable form of primary aldosteronism Cushing syndrome due to ectopic ACTH secretion ACTH-dependent Cushing syndrome Familial papillary or follicular thyroid carcinoma ACTH-independent Cushing syndrome Familial nonmedullary thyroid carcinoma Familial hyperreninemic hypoaldosteronism type 2 Familial hyperreninemic hypoaldosteronism type 1 IMAGe syndrome Familial medullary thyroid carcinoma Rare adrenal disease Acute adrenal insufficiency Von Hippel-Lindau disease Chronic primary adrenal insufficiency Primary adrenal insufficiency Genetic chronic primary adrenal insufficiency Acquired chronic primary adrenal insufficiency Congenital lipoid adrenal hyperplasia due to STAR deficency Familial glucocorticoid deficiency Familial adrenal hypoplasia with absent pituitary luteinizing hormone Classic congenital lipoid adrenal hyperplasia due to STAR deficency Rare disease with adrenal Cushing syndrome as a major feature Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Waterhouse-Friderichsen syndrome X-linked adrenal hypoplasia congenita Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency Congenital adrenal hypoplasia of maternal cause Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency Cushing disease Somatotropic adenoma Prolactinoma Multiple endocrine neoplasia Functioning gonadotropic adenoma Multiple paragangliomas associated with polycythemia Multiple endocrine neoplasia type 4 TSH-secreting pituitary adenoma Functioning pituitary adenoma Medullary thyroid carcinoma Generalized glucocorticoid resistance syndrome Non-functioning pituitary adenoma Neoplasie, endokrine multiple, Typ 1 Nebennierenhyperplasie, kongenitale, durch 21-Hydroxylase-Mangel, klassische Form, einfach virilisierend Neoplasie, endokrine multiple, Typ 2 Hypophysenadenom, gemischt-aktives Nebennierenhyperplasie, kongenitale, durch 21-Hydroxylase-Mangel, klassische Form mit Salzverlust Pseudo-Leprechaunismus-Syndrom Typ Patterson Störung der Geschlechtsentwicklung 46,XY - Nebenniereninsuffizienz, durch CYP11A1-Mangel Hyperaldosteronismus, familiärer Seltenes Schilddrüsenkarzinom CBG (Cortisol-bindendes Globulin)-Mangel Cushing-Syndrom durch bilaterale makronoduläre Nebennierenhyperplasie Nelson-Syndrom Seltener Tumor der Nebenschilddrüse Hypophysenadenom Infertilität, seltene Tumor, adrenaler/paraganglialer Somatomammotropinom Nebennierenhyperplasie, primäre unilaterale Nebenniereninsuffizienz, isolierte vererbte, durch CYP11A1-Mangel Hypophysenadenom, isoliertes familiäres Primäre pigmentierte noduläre adrenokortikale Krankheit Adenom, Aldosteron-produzierendes Hyperaldosteronismus, familiärer, Typ I Hyperaldosteronismus, familiärer, Typ II Carney-Komplex Null-Zell-Hypophysenadenom Adrenoleukodystrophie, X-chromosomale, zerebrale Form Schilddrüsenkarzinom, anaplastisches Adrenales Cushing-Syndrom Hypophysenadenom, stummes Autoimmun-Polyendokrinopathie Typ 2 Nebenschilddrüsen-Karzinom Adrenokortikales Karzinom Cushing-Syndrom, endogenes Hyperandrogenismus durch Cortison-Reduktase-Mangel Cushing-Syndrom Akromegalie Nebennierenhyperplasie, kongenitale Schilddrüsenkarzinom, differenziertes Adrenomyeloneuropathie Multiple endokrine Neoplasie Typ 2A Hyperaldosteronismus, primärer, seltener McCune-Albright-Syndrom Hypoaldosteronismus, familiärer Phaeochromozytom, sporadisches Hypoaldosteronismus, seltener Phäochromozytom-Paragangliom-Syndrom, hereditäres Paragangliom, sezernierendes sporadisches Adrenomyodystrophie Gigantismus, hypophysärer Sporadisches Phaeochromozytom/sezernierendes Paragangliom Hyperparathyreoidismus, familiärer primärer Multiple endokrine Neoplasie Typ 2B