Combined pituitary hormone deficiencies, genetic forms

Orpha code: 95494OMIM code: 613986

Definicja

Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy.

Disease data
Klasyfikacja

Disease

Synonimy
Familial congenital hypopituitarism
Rodzinna wrodzona niedoczynność przysadki
Złożone niedobory hormonów przysadki, formy genetyczne
Multiple pituitary hormone deficiencies, genetic forms
Kod ORPHA
95494
Kod OMIM
613986
Kod ICD10
E23.0
Kod ICD11
-

No additional description.

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