Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare genetic pituitary disease characterized by variable deficiency of all hormones produced in the anterior lobe of the pituitary gland. Clinical manifestations include hypothyroidism, hypogonadism, growth retardation and short stature, and secondary adrenal insufficiency. Age of onset is variable. Signs and symptoms usually develop gradually, and loss of the different hormones is often sequential. Disease data Klasyfikacja Disease Synonimy Genetic panhypopituitarism Genetic panhypopituitarism Kod ORPHA 90695 Kod OMIM 312000 Kod ICD10 E23.0 Kod ICD11 5A61.0 *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl