SE-ATLAS

Insuffisance hypophysaire d'origine vasculaire Syndrome avec hypoparathyroïdie Apoplexie hypophysaire Polyendocrinopathie auto-immune type 2 Polyendocrinopathie auto-immune Insuffisance hypophysaire secondaire à une maladie de surcharge Hypoparathyroïdie rare Acromégalie Insuffisance hypophysaire d'origine granulomateuse Insuffisance hypophysaire d'origine post-traumatique Hypogonadisme hypogonadotrope congénital Insuffisance hypophysaire non acquise Diabète insipide central acquis Maladie associée à une insuffisance hypophysaire multiple non acquise Hypocalcémie autosomique dominante Hypoparathyroïdie isolée familiale par défaut de sécrétion de la PTH Déficits hypohysaires multiples de cause génétique identifée Gigantisme hypophysaire Hypogonadisme hypogonadotrope congénital sans anosmie Rupture de la tige pituitaire Petite taille par déficit en GHSR Neurohypophysite infundibulaire Déficit congénital isolé en ACTH Maladie d'Addison Insuffisance hypophysaire d'origine tumorale Insuffisance hypophysaire acquise Hypophysite primitive Insuffisance hypophysaire d'origine méningée Déficit isolé tardif en ACTH Tumeur de l'hypophyse Adénohypophysite Insuffisance hypophysaire multiple non acquise sans malformations extra-hypophysaires associées Kyste arachnoïdien Gliome des voies optiques Panhypophysite Craniopharyngiome Méningiome Diabète insipide d'origine centrale Chordome Polyendocrinopathie auto-immune type 1 Hémorragie massive bilatérale des surrénales 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 Isolated follicle stimulating hormone deficiency Somatomammotropinoma Rare disorder with multisystemic involvement and congenital hypogonadotropic hypogonadism Endocrinopathy with congenital hypogonadotropic hypogonadism as a major feature Familial isolated pituitary adenoma Non-acquired panhypopituitarism Null pituitary adenoma Silent pituitary adenoma Adrenogenital syndrome