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Non-acquired combined pituitary hormone deficiency

rare

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.

Identifiers
MONDO:0018762 Orphanet:467
Part of
Non-acquired pituitary hormone deficiency
Also known as
congenital combined pituitary hormone deficiency · congenital hypopituitarism

Subtypes

All diseases Rare only
Disease Subtypes
Holoprosencephaly 20
Pallister-Hall syndrome 1
ANE syndrome
Deficiency in anterior pituitary function - variable immunodeficiency syndrome
Non-acquired combined pituitary hormone deficiency with spine abnormalities
Postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome
Short stature-pituitary and cerebellar defects-small sella turcica syndrome

Rare disease

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