SE-ATLAS

46,XY difference of sex development-adrenal insufficiency due to CYP11A1 deficiency ACTH-dependent Cushing syndrome ACTH-independent Cushing syndrome Acquired chronic primary adrenal insufficiency Acromegaly Acute adrenal insufficiency Addison disease Adrenal Cushing syndrome Adrenal/paraganglial tumor Adrenocortical carcinoma Adrenocortical carcinoma with pure aldosterone hypersecretion Adrenomyeloneuropathy Adrenomyodystrophy Aldosterone-producing adenoma Anaplastic thyroid carcinoma Apparent mineralocorticoid excess Autoimmune polyendocrinopathy type 1 Autoimmune polyendocrinopathy type 2 Bilateral massive adrenal hemorrhage Carney complex Catecholamine-producing tumor Chronic primary adrenal insufficiency Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form Classic congenital lipoid adrenal hyperplasia due to STAR deficency Congenital adrenal hyperplasia Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Congenital adrenal hypoplasia of maternal cause Congenital lipoid adrenal hyperplasia due to STAR deficency Corticosteroid-binding globulin deficiency Cushing disease Cushing syndrome Cushing syndrome due to bilateral macronodular adrenocortical disease Cushing syndrome due to ectopic ACTH secretion Differentiated thyroid carcinoma Ectopic aldosterone-producing tumor Endogenous Cushing syndrome Familial adrenal hypoplasia with absent pituitary luteinizing hormone Familial glucocorticoid deficiency Familial hyperaldosteronism Familial hyperaldosteronism type I Familial hyperaldosteronism type II Familial hyperaldosteronism type III Familial hyperreninemic hypoaldosteronism type 1 Familial hyperreninemic hypoaldosteronism type 2 Familial hypoaldosteronism Familial isolated hyperparathyroidism Familial isolated pituitary adenoma Familial medullary thyroid carcinoma Familial nonmedullary thyroid carcinoma Familial papillary or follicular thyroid carcinoma Familial papillary thyroid carcinoma with renal papillary neoplasia Familial parathyroid adenoma Familial primary hyperparathyroidism Functioning gonadotropic adenoma Functioning pituitary adenoma Generalized glucocorticoid resistance syndrome Genetic chronic primary adrenal insufficiency Hereditary pheochromocytoma-paraganglioma Hyperandrogenism due to cortisone reductase deficiency Hyperparathyroidism-jaw tumor syndrome IMAGe syndrome Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency McCune-Albright syndrome Medullary thyroid carcinoma Mixed functioning pituitary adenoma Multiple endocrine neoplasia Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 2B Multiple endocrine neoplasia type 4 Multiple paragangliomas associated with polycythemia Nelson syndrome Neonatal adrenoleukodystrophy Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency Non-functioning pituitary adenoma Null pituitary adenoma Parathyroid carcinoma Pituitary adenoma Pituitary carcinoma Pituitary gigantism Pituitary tumor Primary adrenal insufficiency Primary hyperaldosteronism-seizures-neurological abnormalities syndrome Primary pigmented nodular adrenocortical disease Primary unilateral adrenal hyperplasia Prolactinoma Pseudoleprechaunism syndrome, Patterson type Rare adrenal disease Rare disease with adrenal Cushing syndrome as a major feature Rare hypoaldosteronism Rare infertility Rare non surgically correctable form of primary aldosteronism Rare parathyroid tumor Rare primary hyperaldosteronism Rare surgically correctable form of primary aldosteronism Rare thyroid carcinoma Silent pituitary adenoma Somatomammotropinoma Somatotropic adenoma Sporadic pheochromocytoma Sporadic pheochromocytoma/secreting paraganglioma Sporadic secreting paraganglioma TSH-secreting pituitary adenoma Triple A syndrome Von Hippel-Lindau disease Waterhouse-Friderichsen syndrome X-linked adrenal hypoplasia congenita X-linked adrenoleukodystrophy X-linked cerebral adrenoleukodystrophy