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 Acromegaly Hypoinsulinemic hypoglycemia and body hemihypertrophy Apparent mineralocorticoid excess Rare endocrine disease Prader-Willi syndrome Neuroendocrine neoplasm Familial hyperinsulinism Turner syndrome Rare adrenal disease Rare dyslipidemia Rare diabetes mellitus Polyendocrinopathy Acute adrenal insufficiency Rare thyroid disease Difference of sex development Pseudohypoparathyroidism Primary adrenal insufficiency Juvenile Paget disease Leydig cell hypoplasia Familial multinodular goiter Pituitary deficiency Autosomal recessive infantile hypercalcemia