SE-ATLAS

46,XX difference of sex development 46,XY difference of sex development ACTH-independent Cushing syndrome due to rare cortisol-producing adrenal tumor Acquired lipodystrophy Acquired pituitary hormone deficiency Acquired premature ovarian failure Acrodysostosis with multiple hormone resistance Adrenal/paraganglial tumor Adrenocortical carcinoma Adrenogenital syndrome Apparent mineralocorticoid excess Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome Autoimmune polyendocrinopathy Autosomal dominant hypocalcemia Autosomal recessive infantile hypercalcemia Bangstad syndrome Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Chronic primary adrenal insufficiency Combined immunodeficiency due to LRBA deficiency Congenital adrenal hyperplasia Congenital hypothyroidism Congenital isolated hyperinsulinism Congenital thyroid malformation without hypothyroidism Corticosteroid-binding globulin deficiency Craniopharyngioma Cushing syndrome Deafness-hypogonadism syndrome Diencephalic syndrome Difference of sex development Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome Disorders of vitamin D metabolism Duplication of the pituitary gland Familial hyperaldosteronism Familial hyperinsulinism Familial hyperprolactinemia Familial hyperthyroidism due to mutations in TSH receptor Familial hypocalciuric hypercalcemia Familial multinodular goiter Familial tumoral calcinosis Gastroenteropancreatic neuroendocrine neoplasm Genetic lipodystrophy Genetic non-syndromic obesity Genetic obesity Growth hormone insensitivity syndrome Hereditary pheochromocytoma-paraganglioma Hydrocephalus-obesity-hypogonadism syndrome Hypergonadotropic hypogonadism-cataract syndrome Hyperinsulinism due to INSR deficiency Hypocalcemic vitamin D-dependent rickets Hypocalcemic vitamin D-resistant rickets Hypogonadism-mitral valve prolapse-intellectual disability syndrome Hypoinsulinemic hypoglycemia and body hemihypertrophy Hypothalamic adipsic hypernatraemia syndrome Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome Mikati-Najjar-Sahli syndrome Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome Multiple polyglandular tumor Neonatal diabetes mellitus Neonatal severe primary hyperparathyroidism Neuroectodermal-endocrine syndrome Neuroendocrine neoplasm Non-acquired pituitary hormone deficiency Non-acquired premature ovarian failure Non-insulinoma pancreatogenous hypoglycemia syndrome Noonan syndrome Obesity due to CEP19 deficiency Obesity due to SIM1 deficiency Obesity due to congenital leptin deficiency Obesity due to congenital leptin resistance Oncogenic osteomalacia Pituitary adenoma Pituitary deficiency Polyendocrinopathy Primary adrenal insufficiency Primary hypergonadotropic hypogonadism-partial alopecia syndrome Primary lipodystrophy Primary pigmented nodular adrenocortical disease Proximal myotonic myopathy Pseudohypoparathyroidism Rare adrenal disease Rare diabetes mellitus Rare diabetes mellitus type 1 Rare diabetes mellitus type 2 Rare disorder with hypergonadotropic hypogonadism Rare dyslipidemia Rare endocrine disease Rare endocrine growth disease Rare genetic thyroid disease Rare hyperlipidemia Rare hyperparathyroidism Rare hyperthyroidism Rare hypoaldosteronism Rare hypolipidemia Rare hypoparathyroidism Rare hypothalamic or pituitary disease Rare hypothyroidism Rare insulin-resistance syndrome Rare parathyroid disease and phosphocalcic metabolism anomaly Rare parathyroid tumor Rare precocious puberty Rare primary hyperaldosteronism Rare syndromic dyslipidemia Rare thyroid disease Rare thyroid tumor Retinohepatoendocrinologic syndrome Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency Sex chromosome difference of sex development Steinert myotonic dystrophy Syndromic obesity Thymic neuroendocrine tumor Turner syndrome Woodhouse-Sakati syndrome X-linked acrogigantism X-linked adrenoleukodystrophy X-linked intellectual disability, Cilliers type X-linked intellectual disability, Van Esch type