SE-ATLAS

Neoplasie, endokrine multiple, Typ 1 Wachstumshormonmangel, isolierter, Typ IA Hyperinsulinismus, diffuser, Diazoxid-sensitiver Störung der Geschlechtsentwicklung 46,XY, durch 5-Alpha-Reduktase 2-Mangel Hyperinsulinismus, kongenitaler, durch Glukokinase-Mangel Neoplasie, endokrine multiple Neoplasie, endokrine multiple, Typ 4 Multiple endokrine Neoplasie Typ 2A Adrenoleukodystrophie, X-chromosomale Hyperinsulinismus, anstrengungsinduzierter Hypogonadotroper Hypogonadismus - frontoparietale Alopezie Adenom, funktionelles gonadotropes Kallmann-Syndrom Nelson-Syndrom Maternal vererbter Diabetes mit Schwerhörigkeit Wachstumshormonmangel, isolierter, Typ IB Autoimmun-Polyendokrinopathie Typ 3 Insulinresistenz-Syndrom Typ B Glukokortikoid-Mangel, familiärer Hypophyseninfarkt Hypophysenadenom Bartter-Syndrom Autoimmun-Polyendokrinopathie Typ 2 Hypogonadotroper Hypogonadismus, isolierter kongenitaler Hyperinsulinismus, fokaler, Diazoxid-resistenter, durch Kir6.2-Mangel Addison-Krankheit Hypoparathyreoidismus, familiärer isolierter Hypophysenadenom, nicht-funktionelles Hyperprolaktinämie, familiäre Hyperinsulinismus durch HNF4A-Mangel Kraniopharyngeom Insulinresistenz-Syndrom Typ A Autoimmun-Polyendokrinopathie Typ 1 Nebennierenhyperplasie, kongenitale, durch Cytochrom-P450-Oxydoreduktase-Mangel Nebennierenhypoplasie, kongenitale, X-chromosomale Cushing-Syndrom durch bilaterale makronoduläre Nebennierenhyperplasie Hypothyreose, kongenitale, idiopathische Wachstumshormonmangel, isolierter, nicht erworbener Störung der Geschlechtsentwicklung 46,XY, durch 17-beta-Hydroxysteroid-Dehydrogenase 3-Mangel Hyperinsulinismus durch Kir6.2-Mangel, autosomal-rezessiver Neoplasie, endokrine multiple, Typ 2 Diabetes insipidus, zentraler Prolaktinom Prader-Willi-Syndrom Nebennierenhyperplasie, kongenitale, durch 21-Hydroxylase-Mangel, klassische Form mit Salzverlust Cushing-Krankheit Silver-Russell-Syndrom Turner-Syndrom Ovardysgenesie-Kleinwuchs-Syndrom Primäre pigmentierte noduläre adrenokortikale Krankheit Hyperinsulinismus durch SUR1-Mangel, autosomal-dominanter Adrenogenitales Syndrom Wachstumshormonmangel, isolierter, Typ II Somatomammotropinom Nebennierenhyperplasie, kongenitale, durch 21-Hydroxylase-Mangel, klassische Form Hyperinsulinismus, fokaler, Diazoxid-resistenter, durch SUR1-Mangel Aromatase-Exzess-Syndrom Hyperaldosteronismus, familiärer Nebennierenhyperplasie, kongenitale, durch 17-alpha-Hydroxylase-Mangel 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 Pituitary deficiency due to Rathke cleft cysts Sheehan syndrome Pituitary deficiency due to empty sella turcica syndrome Isolated growth hormone deficiency type III Hyperinsulinism due to INSR deficiency Familial hyperaldosteronism type III Familial hyperaldosteronism type I Familial hyperaldosteronism type II Familial isolated pituitary adenoma Pediatric-onset Graves disease Non-acquired combined pituitary hormone deficiency MODY Isolated permanent neonatal diabetes mellitus Cushing syndrome due to ectopic ACTH secretion Non-acquired panhypopituitarism Hyperandrogenism due to cortisone reductase deficiency Autoimmune polyendocrinopathy type 4 Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency Congenital lipoid adrenal hyperplasia due to STAR deficency Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency 46,XY difference of sex development due to isolated 17,20-lyase deficiency 46,XY difference of sex development due to testicular 17,20-desmolase deficiency Autosomal recessive hyperinsulinism due to SUR1 deficiency Wolfram-like syndrome Acromegaly Insulin autoimmune syndrome Hyperinsulinism due to HNF1A deficiency Hyperinsulinism-hyperammonemia syndrome