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combined pituitary hormone deficiencies, genetic form

Disease Summary
Associated Targets (23)
Tbio

17

Tclin

4

Tchem

2


Explore Associated Targets
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0013099:  combined pituitary hormone deficiencies, genetic form
GARD:0002252: 
GARD:0010602: 
OMIMPS:613038: 
Orphanet:95494: 
SCTID:718182008: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)
No novelty measurements found