SE-ATLAS

Turner syndrome Prader-Willi syndrome Hypothyroidism due to deficient transcription factors involved in pituitary development or function Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome Non-acquired pituitary hormone deficiency Combined pituitary hormone deficiencies, genetic forms Pituitary stalk interruption syndrome Congenital hypothyroidism due to maternal intake of antithyroid drugs Johanson-Blizzard syndrome Genetic transient congenital hypothyroidism Non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome Muscular pseudohypertrophy-hypothyroidism syndrome Hypothyroidism due to TSH receptor mutations Laron syndrome with immunodeficiency McCune-Albright syndrome Allan-Herndon-Dudley syndrome Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome Non-acquired panhypopituitarism Autoimmune polyendocrinopathy type 2 Isolated congenital hypogonadotropic hypogonadism Laurence-Moon syndrome Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome Aromatase deficiency Neonatal iodine exposure Pituitary resistance to thyroid hormone Transient congenital hypothyroidism due to neonatal factor Transient congenital hypothyroidism due to maternal factor Cataract-intellectual disability-hypogonadism syndrome Bardet-Biedl syndrome Congenital isolated ACTH deficiency Classic galactosemia Septopreoptic holoprosencephaly CHARGE syndrome Short stature due to primary acid-labile subunit deficiency Ataxia-hypogonadism-choroidal dystrophy syndrome Pallister-Hall syndrome Congenital adrenal hyperplasia Isolated follicle stimulating hormone deficiency Congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency Congenital lipoid adrenal hyperplasia due to STAR deficency Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency Aromatase excess syndrome Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency Normosmic congenital hypogonadotropic hypogonadism Short stature due to partial GHR deficiency Short stature-delayed bone age due to thyroid hormone metabolism deficiency Congenital hypothyroidism Short stature due to GHSR deficiency Pendred syndrome Short stature-pituitary and cerebellar defects-small sella turcica syndrome Hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Non-acquired combined pituitary hormone deficiency Familial adrenal hypoplasia with absent pituitary luteinizing hormone X-linked adrenal hypoplasia congenita Kallmann syndrome Athyreosis Semilobar holoprosencephaly Congenital hypothyroidism due to transplacental passage of TSH-binding inhibitory antibodies Primary congenital hypothyroidism without thyroid developmental anomaly Alobar holoprosencephaly Idiopathic congenital hypothyroidism Lobar holoprosencephaly X-linked central congenital hypothyroidism with late-onset testicular enlargement Isolated thyroid-stimulating hormone deficiency Growth delay due to insulin-like growth factor I resistance Growth delay due to insulin-like growth factor type 1 deficiency Rare endocrine growth disease Isolated thyrotropin-releasing hormone deficiency Septo-optic dysplasia spectrum Deficiency in anterior pituitary function-variable immunodeficiency syndrome Fetal iodine syndrome Non-acquired isolated growth hormone deficiency Laron syndrome Rare peripheral precocious puberty Autoimmune polyendocrinopathy type 1 Blepharophimosis-ptosis-epicanthus inversus syndrome Transient congenital hypothyroidism Woodhouse-Sakati syndrome Syndrom der Wachstumshormoninsensivität Vorzeitige männliche Pubertät, familiäre Form Seltene Form der vorzeitigen Pubertät Kongenitale Hypothyreose durch Entwicklungsanomalie Schilddrüsenektopie Schilddrüsen-Dyshormonogenese, familiäre Schilddrüsenhemiagenesie Schilddrüsenhypoplasie Gonadendysgenesie, 46, XX-Typ Hypothyreose, kongenitale primäre Hypothyreose, kongenitale permanente Hypothyreose, kongenitale zentrale Thyrotropin-Releasing-Hormon (TRH)-Resistenz Hypogonadotroper Hypogonadismus, kongenitaler