SE-ATLAS

Rare parathyroid disease and phosphocalcic metabolism anomaly Genetic obesity Hypocalcemic rickets Neonatal diabetes mellitus Disorders of vitamin D metabolism Acquired premature ovarian failure Rare precocious puberty Prolactinoma Familial hyperprolactinemia Noonan syndrome Rare diabetes mellitus type 1 Duplication of the pituitary gland 46,XX gonadal dysgenesis Rare insulin-resistance syndrome Congenital thyroid malformation without hypothyroidism Rare diabetes mellitus type 2 Rare thyroid tumor Familial tumoral calcinosis Corticosteroid-binding globulin deficiency Adrenal/paraganglial tumor Pituitary adenoma Rare parathyroid tumor Rare hypothalamic or pituitary disease Other rare diabetes mellitus Growth hormone insensitivity syndrome Rare endocrine growth disease Rare hypothyroidism Silver-Russell syndrome Familial hypocalciuric hypercalcemia Primary lipodystrophy Rare hyperthyroidism Rare hypoparathyroidism Cushing syndrome Congenital adrenal hyperplasia Rare hyperparathyroidism Non-acquired pituitary hormone deficiency Adrenogenital syndrome Rare hypoaldosteronism McCune-Albright syndrome Rare primary hyperaldosteronism Rare hyperlipidemia Hypochondroplasia Multiple endocrine neoplasia type 2B Multiple endocrine neoplasia type 2A Multiple endocrine neoplasia type 4 Multiple endocrine neoplasia type 2 Non-acquired premature ovarian failure Multiple endocrine neoplasia Multiple endocrine neoplasia type 1 Hypophosphatemic rickets Rare hypolipidemia Addison disease Congenital hypothyroidism X-linked acrogigantism Diencephalic syndrome Rare syndromic dyslipidemia Craniopharyngioma Aldosterone-producing adenoma Rare disorder with hypergonadotropic hypogonadism Akromegalie Hypoinsulinämische Hypoglykämie - Hemihypertrophie Apparenter Mineralocorticoid Exzess Endokrine Krankheit, seltene Prader-Willi-Syndrom Tumor, neuroendokriner Hyperinsulinismus, familiärer Turner-Syndrom Nebennierenkrankheit, seltene Dyslipidämie, seltene Diabetes mellitus, seltener Polyendokrinopathie Nebenniereninsuffizienz, akute Schilddrüsenkrankheit, seltene Störung der Geschlechtsentwicklung Pseudohypoparathyreoidismus Nebenniereninsuffizienz, primäre Paget-Syndrom, juveniles Leydig-Zell-Hypoplasie Familiärer multinodulärer Kropf Hypophysenfunktionsstörung Hyperkalzämie, infantile, autosomal-rezessive