SE-ATLAS

Pituitary hormone deficiency of vascular origin Syndrome with hypoparathyroidism Pituitary apoplexy Autoimmune polyendocrinopathy type 2 Autoimmune polyendocrinopathy Pituitary hormone deficiency secondary to storage disease Rare hypoparathyroidism Acromegaly Pituitary hormone deficiency secondary to a granulomatous disease Post-traumatic pituitary deficiency Congenital hypogonadotropic hypogonadism Non-acquired pituitary hormone deficiency Acquired central diabetes insipidus Disease associated with non-acquired combined pituitary hormone deficiency Autosomal dominant hypocalcemia Familial isolated hypoparathyroidism due to impaired PTH secretion Combined pituitary hormone deficiencies, genetic forms Pituitary gigantism Normosmic congenital hypogonadotropic hypogonadism Pituitary stalk interruption syndrome Short stature due to GHSR deficiency Infundibulo-neurohypophysitis Congenital isolated ACTH deficiency Addison disease Pituitary hormone deficiency of tumoral origin Acquired pituitary hormone deficiency Primary hypophysitis Pituitary hormone deficiency of meningeal origin Late-onset isolated ACTH deficiency Pituitary tumor Adenohypophysitis Non-acquired combined pituitary hormone deficiencies without extrapituitary malformations Arachnoid cyst Optic pathway glioma Panhypophysitis Craniopharyngioma Meningioma Central diabetes insipidus Chordoma Autoimmune polyendocrinopathy type 1 Bilateral massive adrenal hemorrhage Pituitary carcinoma Familial isolated hypoparathyroidism Familial isolated hypoparathyroidism due to agenesis of parathyroid gland Non-acquired combined pituitary hormone deficiency Autoimmune polyendocrinopathy type 3 Kallmann syndrome Isolated growth hormone deficiency type IA Acute adrenal insufficiency Secondary hypoparathyroidism due to impaired parathormon secretion Pseudohypoparathyroidism Pituitary deficiency Autoimmune polyendocrinopathy type 4 Isolated growth hormone deficiency type IB Short stature due to growth hormone qualitative anomaly Non-acquired isolated growth hormone deficiency Autoimmune hypoparathyroidism Isolated growth hormone deficiency type II Waterhouse-Friderichsen syndrome Functioning pituitary adenoma Cushing disease Somatotropic adenoma Functioning gonadotropic adenoma Prolactinoma Hereditary central diabetes insipidus Isolated growth hormone deficiency type III TSH-secreting pituitary adenoma Non-functioning pituitary adenoma Germinoma of the central nervous system Pituitary dermoid and epidermoid cysts Mixed functioning pituitary adenoma Aldosterone-producing adenoma Pituitary deficiency due to Rathke cleft cysts Pituitary deficiency due to empty sella turcica syndrome Rare disease with adrenal Cushing syndrome as a major feature Cushing syndrome due to ectopic ACTH secretion ACTH-independent Cushing syndrome ACTH-dependent Cushing syndrome Endogenous Cushing syndrome Adrenal Cushing syndrome Cushing syndrome due to bilateral macronodular adrenocortical disease Isolated thyroid-stimulating hormone deficiency Sheehan syndrome Pituitary adenoma Nelson syndrome Sarcoidosis Tuberculosis Isolated congenital hypogonadotropic hypogonadism Follicle-Stimulating Hormone (FSH)-Mangel, isolierter Somatomammotropinom Seltene Störung mit multisystemischer Beteiligung und kongenitalen hypogonadotropen Hypogonadismus Endokrinopathie mit kongenitalen hypogonadotropen Hypogonadismus als Hauptmerkmal Hypophysenadenom, isoliertes familiäres Panhypopituitarismus, genetisch bedingter Null-Zell-Hypophysenadenom Hypophysenadenom, stummes Adrenogenitales Syndrom