SE-ATLAS

Rare dyslipidemia Nelson syndrome ACTH-dependent Cushing syndrome Multiple endocrine neoplasia type 2A Autoimmune polyendocrinopathy Multiple endocrine neoplasia type 2B Aldosterone-producing adenoma Acromegaly Rare disease with adrenal Cushing syndrome as a major feature Cushing syndrome due to bilateral macronodular adrenocortical disease Adrenal Cushing syndrome Endogenous Cushing syndrome X-linked adrenoleukodystrophy Cushing syndrome due to ectopic ACTH secretion Autoimmune hypoparathyroidism Medullary thyroid carcinoma ACTH-independent Cushing syndrome Rare diabetes mellitus Autoimmune polyendocrinopathy type 2 Hypocalcemic rickets Carney complex Pituitary adenoma X-linked hypophosphatemia Pseudohypoparathyroidism type 1A Complete androgen insensitivity syndrome Neuroendocrine neoplasm Bartter syndrome 46,XY partial gonadal dysgenesis Von Hippel-Lindau disease Autoimmune polyendocrinopathy type 1 Mixed functioning pituitary adenoma Multiple endocrine neoplasia type 1 Multiple endocrine neoplasia type 2 Autoimmune polyendocrinopathy type 3 Anaplastic thyroid carcinoma Parathyroid carcinoma Zollinger-Ellison syndrome Differentiated thyroid carcinoma Difference of sex development Addison disease Prolactinoma Rare hyperthyroidism Familial hypocalciuric hypercalcemia Autoimmune polyendocrinopathy type 4 Rare hypothyroidism Autosomal recessive hypophosphatemic rickets Familial primary hyperparathyroidism Congenital adrenal hyperplasia Familial hyperaldosteronism Rare primary hyperaldosteronism 46,XX difference of sex development Adrenogenital syndrome Familial multinodular goiter Partial androgen insensitivity syndrome Sex chromosome difference of sex development Acute adrenal insufficiency Multiple endocrine neoplasia type 4 Rare disorder with hypergonadotropic hypogonadism Multiple endocrine neoplasia Functioning neuroendocrine tumor of pancreas Phenylketonuria TSH-secreting pituitary adenoma Functioning gonadotropic adenoma Non-functioning neuroendocrine tumor of pancreas Acquired premature ovarian failure Adrenocortical carcinoma Gastroenteric neuroendocrine neoplasm Pheochromocytoma-paraganglioma Neuroendocrine tumor of stomach Serotonin-producing neuroendocrine tumor of pancreas Neuroendocrine neoplasm of appendix 46,XY difference of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency 46,XY difference of sex development due to 5-alpha-reductase 2 deficiency 46,XY complete gonadal dysgenesis Neuroendocrine tumor of anal canal Central precocious puberty Adrenal/paraganglial tumor Somatotropic adenoma Resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta Neuroendocrine tumor of the rectum Rare thyroid carcinoma Carcinoid syndrome Cushing disease PPoma Turner syndrome Glucagonoma Somatostatinoma VIPoma Genetic obesity Neuroendocrine tumor of small intestine Liddle syndrome Acquired pituitary hormone deficiency Primary hypophysitis Neuroendocrine neoplasm of esophagus 46,XY difference of sex development Mayer-Rokitansky-Küster-Hauser syndrome Persistent Müllerian duct syndrome Pseudohypoparathyroidism Pseudopseudohypoparathyroidism Pseudohypoparathyroidism type 1C Central diabetes insipidus Pseudohypoparathyroidism type 1B 46,XX testicular difference of sex development Pseudohypoparathyroidism type 2 Tetragametic chimerism Nebennierenhyperplasie, kongenitale, durch 3-beta-Hydroxysteroid-Dehydrogenase-Mangel Nebennierenhyperplasie, kongenitale, durch 17-alpha-Hydroxylase-Mangel Nebennierenhyperplasie, kongenitale, durch 11-beta-Hydroxylase-Mangel Nebennierenhyperplasie, kongenitale, durch 21-Hydroxylase-Mangel, klassische Form Hypophosphatämische Rachitis Hypospadie, posteriore, nicht-syndromale Resistenz gegen Schilddrüsenhormone durch Mutation im Thyroidhormonrezeptor alpha Neuroendokriner Tumor des Pankreas Insulinom Ovarialinsuffizienz, vorzeitige, nicht-erworbene Klinefelter-Syndrom 45,X/46,XY-Gonadendysgenesie, gemischte