Non-acquired combined pituitary hormone deficiency
MONDO:0018762Congenital 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.
Also known as: congenital combined pituitary hormone deficiency, congenital hypopituitarism
9 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Congenital hypothalamic hamartoma syndrome
(2)
Alobar holoprosencephaly
(0)
ANE syndrome
(0)
Chromosome 1q41-q42 deletion syndrome
(0)
Deficiency in anterior pituitary function - variable immunodeficiency syndrome
(0)
Holoprosencephaly
(0)
Holoprosencephaly 1
(0)
Holoprosencephaly 10
(0)
Holoprosencephaly 11
(0)
Holoprosencephaly 12 with or without pancreatic agenesis
(0)
Holoprosencephaly 13, X-linked
(0)
Holoprosencephaly 14
(0)
Holoprosencephaly 2
(0)
Holoprosencephaly 3
(0)
Holoprosencephaly 4
(0)
Holoprosencephaly 5
(0)
Holoprosencephaly 6
(0)
Holoprosencephaly 7
(0)
Holoprosencephaly 8
(0)
Holoprosencephaly 9
(0)