SE-ATLAS

Corticosurrénalome Cancer différencié de la thyroïde Néoplasie endocrinienne multiple type 2A Syndrome de McCune-Albright Néoplasie endocrinienne multiple type 2B Syndrome de délétion 22q11.2 Maladie d'Addison Insuffisance hypophysaire d'origine tumorale Insuffisance hypophysaire d'origine méningée Syndrome de Cushing indépendant de l'ACTH Hyperinsulinisme congénital isolé Glycogénose par déficit en glucose-6-phosphatase Syndrome de Kallmann Maladie rare de la thyroïde Polyendocrinopathie auto-immune type 4 Néoplasie endocrinienne multiple Néoplasie endocrinienne multiple type 4 Phéochromocytome sporadique Syndrome de Fanconi-Bickel Hyperinsulinisme familial Résistance hypophysaire aux hormones thyroïdiennes Diabète de type 2 rare Néoplasie endocrinienne multiple type 2 Carcinome parathyroidien Hyperthyroïdie rare Hypothyroïdie rare Hyperaldostéronisme primitif rare Phéochromocytome/paragangliome sécrétant sporadique Néoplasie endocrinienne multiple type 1 Résistance généralisée aux hormones thyroïdiennes Syndrome adrenogenital Insuffisance surrénalienne aiguë Diabète insipide central héréditaire Pseudo-hypoparathyroïdie Syndrome de Cushing par sécrétion ectopique d'ACTH Syndrome de Cushing dépendant de l'ACTH Syndrome de Cushing endogène Syndrome de Cushing surrénalien Maladie rare avec un syndrome de Cushing surrénalien comme manifestation majeure Maladie de Cushing Hypoparathyroïdie auto-immune Adénome producteur d'aldostérone Hypoaldostéronisme rare 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 syndrome Gitelman syndrome Hereditary pheochromocytoma-paraganglioma Rare hypoparathyroidism Waterhouse-Friderichsen syndrome Rare thyroid carcinoma Non-acquired pituitary hormone deficiency Glycogen storage disease due to aldolase A deficiency Overgrowth/obesity syndrome Overgrowth syndrome Neonatal adrenoleukodystrophy Apparent mineralocorticoid excess Rare diabetes mellitus Rare adrenal disease Craniopharyngioma Pituitary deficiency Rare endocrine growth disease Autoimmune polyendocrinopathy type 2 Primary adrenal insufficiency Corticosteroid-binding globulin deficiency Autoimmune polyendocrinopathy Glycogen storage disease Neuroendocrine neoplasm Glycogen storage disease due to acid maltase deficiency Glycogen storage disease due to glycogen debranching enzyme deficiency Central diabetes insipidus 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 Short stature due to growth hormone qualitative anomaly Rare diabetes mellitus type 1 Autoimmune polyendocrinopathy type 1 Pituitary gigantism Autoimmune polyendocrinopathy type 3 Congenital adrenal hyperplasia Familial hyperthyroidism due to mutations in TSH receptor Familial multinodular goiter Congenital hypothyroidism Rare adult hypothyroidism Congenital thyroid malformation without hypothyroidism Thyroid hypoplasia Familial gestational hyperthyroidism Syndromic obesity Rare thyroid tumor Adrenal/paraganglial tumor