SE-ATLAS

Addison disease Adrenocortical carcinoma with pure aldosterone hypersecretion Catecholamine-producing tumor Familial parathyroid adenoma Familial isolated hyperparathyroidism Familial papillary thyroid carcinoma with renal papillary neoplasia Primary hyperaldosteronism-seizures-neurological abnormalities syndrome Familial hyperaldosteronism type III Ectopic aldosterone-producing tumor X-linked adrenoleukodystrophy Hyperparathyroidism-jaw tumor syndrome Autoimmune polyendocrinopathy type 1 Pituitary tumor Neonatal adrenoleukodystrophy Bilateral massive adrenal hemorrhage Rare surgically correctable form of primary aldosteronism Pituitary carcinoma Apparent mineralocorticoid excess Triple A syndrome Rare non surgically correctable form of primary aldosteronism Cushing syndrome due to ectopic ACTH secretion ACTH-dependent Cushing syndrome Familial papillary or follicular thyroid carcinoma ACTH-independent Cushing syndrome Familial nonmedullary thyroid carcinoma Familial hyperreninemic hypoaldosteronism type 2 Familial hyperreninemic hypoaldosteronism type 1 IMAGe syndrome Familial medullary thyroid carcinoma Rare adrenal disease Acute adrenal insufficiency Von Hippel-Lindau disease Chronic primary adrenal insufficiency Primary adrenal insufficiency Genetic chronic primary adrenal insufficiency Acquired chronic primary adrenal insufficiency 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