SE-ATLAS

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