SE-ATLAS

ACTH-dependent Cushing syndrome ACTH-independent Cushing syndrome Acquired central diabetes insipidus Acquired pituitary hormone deficiency Acromegaly Acute adrenal insufficiency Addison disease Adenohypophysitis Adrenal Cushing syndrome Adrenogenital syndrome Aldosterone-producing adenoma Arachnoid cyst Autoimmune hypoparathyroidism Autoimmune polyendocrinopathy Autoimmune polyendocrinopathy type 1 Autoimmune polyendocrinopathy type 2 Autoimmune polyendocrinopathy type 3 Autoimmune polyendocrinopathy type 4 Autosomal dominant hypocalcemia Bilateral massive adrenal hemorrhage Central diabetes insipidus Chordoma Combined pituitary hormone deficiencies, genetic forms Congenital hypogonadotropic hypogonadism Congenital isolated ACTH deficiency Craniopharyngioma Cushing disease Cushing syndrome due to bilateral macronodular adrenocortical disease Cushing syndrome due to ectopic ACTH secretion Disease associated with non-acquired combined pituitary hormone deficiency Endocrinopathy with congenital hypogonadotropic hypogonadism as a major feature Endogenous Cushing syndrome Familial isolated hypoparathyroidism Familial isolated hypoparathyroidism due to agenesis of parathyroid gland Familial isolated hypoparathyroidism due to impaired PTH secretion Familial isolated pituitary adenoma Functioning gonadotropic adenoma Functioning pituitary adenoma Germinoma of the central nervous system Hereditary central diabetes insipidus Infundibulo-neurohypophysitis Isolated congenital hypogonadotropic hypogonadism Isolated follicle stimulating hormone deficiency Isolated growth hormone deficiency type IA Isolated growth hormone deficiency type IB Isolated growth hormone deficiency type II Isolated growth hormone deficiency type III Isolated thyroid-stimulating hormone deficiency Kallmann syndrome Late-onset isolated ACTH deficiency Meningioma Mixed functioning pituitary adenoma Nelson syndrome Non-acquired combined pituitary hormone deficiencies without extrapituitary malformations Non-acquired combined pituitary hormone deficiency Non-acquired isolated growth hormone deficiency Non-acquired panhypopituitarism Non-acquired pituitary hormone deficiency Non-functioning pituitary adenoma Normosmic congenital hypogonadotropic hypogonadism Null pituitary adenoma Optic pathway glioma Panhypophysitis Pituitary adenoma Pituitary apoplexy Pituitary carcinoma Pituitary deficiency Pituitary deficiency due to Rathke cleft cysts Pituitary deficiency due to empty sella turcica syndrome Pituitary dermoid and epidermoid cysts Pituitary gigantism Pituitary hormone deficiency of meningeal origin Pituitary hormone deficiency of tumoral origin Pituitary hormone deficiency of vascular origin Pituitary hormone deficiency secondary to a granulomatous disease Pituitary hormone deficiency secondary to storage disease Pituitary stalk interruption syndrome Pituitary tumor Post-traumatic pituitary deficiency Primary hypophysitis Prolactinoma Pseudohypoparathyroidism Rare disease with adrenal Cushing syndrome as a major feature Rare disorder with multisystemic involvement and congenital hypogonadotropic hypogonadism Rare hypoparathyroidism Sarcoidosis Secondary hypoparathyroidism due to impaired parathormon secretion Sheehan syndrome Short stature due to GHSR deficiency Short stature due to growth hormone qualitative anomaly Silent pituitary adenoma Somatomammotropinoma Somatotropic adenoma Syndrome with hypoparathyroidism TSH-secreting pituitary adenoma Tuberculosis Waterhouse-Friderichsen syndrome