SE-ATLAS

Maladie d'Addison Carcinome corticosurrénalien à hypersécrétion pure d'aldostérone Tumeur sécrétrice de catécholamines Adénome parathyroïdien familial Hyperparathyroïdie isolée familiale Cancer familial papillaire de la thyroïde avec néoplasie rénale papillaire Syndrome d'hyperaldostéronisme primitif-épilepsie-anomalies neurologiques Hyperaldostéronisme familial type III Tumeur ectopique sécrétrice d'aldostérone Adrénoleucodystrophie liée à l'X Syndrome d'hyperparathyroïdie-tumeur mandibulaire Polyendocrinopathie auto-immune type 1 Tumeur de l'hypophyse Adrénoleucodystrophie néonatale Hémorragie massive bilatérale des surrénales Hyperaldostéronisme primitif rare traitable chirurgicalement Carcinome hypophysaire Excès apparent de minéralocorticoïdes Syndrome triple A Hyperaldostéronisme primitif rare non traitable chirurgicalement Syndrome de Cushing par sécrétion ectopique d'ACTH Syndrome de Cushing dépendant de l'ACTH Carcinome papillaire ou folliculaire familial de la thyroïde Syndrome de Cushing indépendant de l'ACTH Carcinome non médullaire familial de la thyroïde Hypoaldostéronisme hyperréninémique familial type 2 Hypoaldostéronisme hyperréninémique familial type 1 Syndrome IMAGe Cancer médullaire de la thyroïde familial Maladie rare des surrénales Insuffisance surrénalienne aiguë Maladie de von Hippel-Lindau Insuffisance surrénale primaire chronique Insuffisance surrénale primaire Insuffisance surrénale primaire chronique génétique Insuffisance surrénale primaire chronique acquise 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 Multiple endocrine neoplasia type 1 Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form Multiple endocrine neoplasia type 2 Mixed functioning pituitary adenoma Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form Pseudoleprechaunism syndrome, Patterson type 46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency Familial hyperaldosteronism Rare thyroid carcinoma Corticosteroid-binding globulin deficiency Cushing syndrome due to bilateral macronodular adrenocortical disease Nelson syndrome Rare parathyroid tumor Pituitary adenoma Rare infertility Adrenal/paraganglial tumor Somatomammotropinoma Primary unilateral adrenal hyperplasia Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency Familial isolated pituitary adenoma Primary pigmented nodular adrenocortical disease Aldosterone-producing adenoma Familial hyperaldosteronism type I Familial hyperaldosteronism type II Carney complex Null pituitary adenoma X-linked cerebral adrenoleukodystrophy Anaplastic thyroid carcinoma Adrenal Cushing syndrome Silent pituitary adenoma Autoimmune polyendocrinopathy type 2 Parathyroid carcinoma Adrenocortical carcinoma Endogenous Cushing syndrome Hyperandrogenism due to cortisone reductase deficiency Cushing syndrome Acromegaly Congenital adrenal hyperplasia Differentiated thyroid carcinoma Adrenomyeloneuropathy Multiple endocrine neoplasia type 2A Rare primary hyperaldosteronism McCune-Albright syndrome Familial hypoaldosteronism Sporadic pheochromocytoma Rare hypoaldosteronism Hereditary pheochromocytoma-paraganglioma Sporadic secreting paraganglioma Adrenomyodystrophy Pituitary gigantism Sporadic pheochromocytoma/secreting paraganglioma Familial primary hyperparathyroidism Multiple endocrine neoplasia type 2B