SE-ATLAS

Adrenokortikales Karzinom Schilddrüsenkarzinom, differenziertes Multiple endokrine Neoplasie Typ 2A McCune-Albright-Syndrom Multiple endokrine Neoplasie Typ 2B 22q11.2-Deletionssyndrom Addison-Krankheit Hypophysenhormon-Mangel, tumorbedingter Hypophysenhormon-Mangel durch meningeale Krankheit Cushing-Syndrom, ACTH-unabhängiges Hyperinsulinismus, isolierter, kongenitaler Glykogenose Typ 1 Kallmann-Syndrom Schilddrüsenkrankheit, seltene Autoimmun-Polyendokrinopathie Typ 4 Neoplasie, endokrine multiple Phaeochromozytom, sporadisches Neoplasie, endokrine multiple, Typ 4 Fanconi-Bickel-Syndrom Hyperinsulinismus, familiärer Hypophysen-Resistenz gegen Schilddrüsenhormone Seltener Diabetes mellitus Typ 2 Nebenschilddrüsen-Karzinom Hyperthyreose, seltene Hypothyreose, seltene Hyperaldosteronismus, primärer, seltener Neoplasie, endokrine multiple, Typ 2 Sporadisches Phaeochromozytom/sezernierendes Paragangliom Neoplasie, endokrine multiple, Typ 1 Generalisierte Resistenz gegen Schilddrüsenhormone Adrenogenitales Syndrom Nebenniereninsuffizienz, akute Hereditärer Arginin-Vasopressin-Mangel Pseudohypoparathyreoidismus Seltene Krankheit mit Cushing-Syndrom als Hauptmerkmal Cushing-Syndrom durch ektopische ACTH-Produktion Cushing-Syndrom, ACTH-abhängiges Cushing-Syndrom, endogenes Adrenales Cushing-Syndrom Cushing-Krankheit Hypoparathyreoidismus, autoimmuner Typ Adenom, Aldosteron-produzierendes Hypoaldosteronismus, seltener Akromegalie Nebennierenhyperplasie, kongenitale, durch 21-Hydroxylase-Mangel, klassische Form Nebennierenhyperplasie, kongenitale, durch 11-beta-Hydroxylase-Mangel Prolaktinom Hypophysenadenom, TSH-sezernierendes Schilddrüsenkarzinom, medulläres Seltene Form der weibliche Infertilität durch genetische Störung der Hypothalamus-Hypophysen-Gonaden-Achse Hypophysenfunktionsstörung durch Empty-Sella-Syndrom Hypophysenadenom Cushing-Syndrom durch bilaterale makronoduläre Nebennierenhyperplasie Nebennierenblutung, bilaterale massive 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 Familial hyperthyroidism due to mutations in TSH receptor Congenital hypothyroidism Congenital thyroid malformation without hypothyroidism Thyroid hypoplasia Familial gestational hyperthyroidism Rare diabetes mellitus Rare adrenal disease Pituitary deficiency Rare endocrine growth disease Primary adrenal insufficiency Autoimmune polyendocrinopathy Short stature due to growth hormone qualitative anomaly Autoimmune polyendocrinopathy type 3 Syndromic obesity Rare thyroid tumor Adrenal/paraganglial tumor Overgrowth/obesity syndrome Neuroendocrine neoplasm Central diabetes insipidus Familial multinodular goiter Rare adult hypothyroidism Glycogen storage disease due to aldolase A deficiency Pituitary deficiency due to Rathke cleft cysts Autoimmune polyendocrinopathy type 1 Corticosteroid-binding globulin deficiency