SE-ATLAS

Multiple endocrine neoplasia type 1 Isolated growth hormone deficiency type IA Diazoxide-sensitive diffuse hyperinsulinism 46,XY difference of sex development due to 5-alpha-reductase 2 deficiency Congenital glucokinase-related hyperinsulinism Multiple endocrine neoplasia Multiple endocrine neoplasia type 4 Multiple endocrine neoplasia type 2A X-linked adrenoleukodystrophy Exercise-induced hyperinsulinism Hypogonadotropic hypogonadism-frontoparietal alopecia syndrome Functioning gonadotropic adenoma Kallmann syndrome Nelson syndrome Maternally-inherited diabetes and deafness Isolated growth hormone deficiency type IB Autoimmune polyendocrinopathy type 3 Insulin-resistance syndrome type B Familial glucocorticoid deficiency Pituitary apoplexy Pituitary adenoma Bartter syndrome Autoimmune polyendocrinopathy type 2 Isolated congenital hypogonadotropic hypogonadism Diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency Addison disease Familial isolated hypoparathyroidism Non-functioning pituitary adenoma Familial hyperprolactinemia Congenital hyperinsulinism due to HNF4A deficiency Craniopharyngioma Insulin-resistance syndrome type A Autoimmune polyendocrinopathy type 1 Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency X-linked adrenal hypoplasia congenita Cushing syndrome due to bilateral macronodular adrenocortical disease Idiopathic congenital hypothyroidism Non-acquired isolated growth hormone deficiency 46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency Autosomal recessive hyperinsulinism due to Kir6.2 deficiency Multiple endocrine neoplasia type 2 Central diabetes insipidus Prolactinoma Prader-Willi syndrome Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form Cushing disease Silver-Russell syndrome Turner syndrome 46,XX ovarian dysgenesis-short stature syndrome Primary pigmented nodular adrenocortical disease Autosomal dominant hyperinsulinism due to SUR1 deficiency Adrenogenital syndrome Isolated growth hormone deficiency type II Somatomammotropinoma Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency Aromatase excess syndrome Familial hyperaldosteronism Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency Generalized glucocorticoid resistance syndrome Multiple endocrine neoplasia type 2B Rare disease with adrenal Cushing syndrome as a major feature ACTH-dependent Cushing syndrome Aldosterone-producing adenoma ACTH-independent Cushing syndrome Endogenous Cushing syndrome Adrenal Cushing syndrome Non-insulinoma pancreatogenous hypoglycemia syndrome Wolfram syndrome Noonan syndrome Rabson-Mendenhall syndrome Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency Hyperinsulinism due to UCP2 deficiency Septo-optic dysplasia spectrum Aromatase deficiency Autosomal dominant hyperinsulinism due to Kir6.2 deficiency Primary unilateral adrenal hyperplasia Acute adrenal insufficiency TSH-secreting pituitary adenoma Hypophysenfunktionsstörung durch Zyste der Rathke-Tasche Sheehan-Syndrom Hypophysenfunktionsstörung durch Empty-Sella-Syndrom Wachstumshormonmangel, isolierter, Typ III Hyperinsulinismus durch INSR-Mangel Hyperaldosteronismus, familiärer, Typ III Hyperaldosteronismus, familiärer, Typ I Hyperaldosteronismus, familiärer, Typ II Hypophysenadenom, isoliertes familiäres Graves-Krankheit mit Beginn im Kindesalter Hypophysenhormon-Mangel, kombinierter, nicht-erworbener MODY Diabetes mellitus, isolierter neonataler permanenter Cushing-Syndrom durch ektopische ACTH-Produktion Panhypopituitarismus, genetisch bedingter Hyperandrogenismus durch Cortison-Reduktase-Mangel Autoimmun-Polyendokrinopathie Typ 4 Nebennierenhyperplasie, kongenitale, durch 3-beta-Hydroxysteroid-Dehydrogenase-Mangel Nebennierenhyperplasie, kongenitale lipoide, durch STAR-Mangel Nebennierenhyperplasie, kongenitale, durch 11-beta-Hydroxylase-Mangel Störung der Geschlechtsentwicklung 46,XY, durch isolierten 17,20-Lyase-Mangel Störung der Geschlechtsentwicklung 46,XY, durch testikulären 17,20-Desmolase-Mangel Hyperinsulinismus durch SUR1-Mangel, autosomal-rezessiver Wolfram-ähnliches Syndrom Akromegalie Antiinsulinantikörper-Syndrom Hyperinsulinismus durch HNF1A-Mangel Hyperinsulinismus-Hyperammonämie-Syndrom