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combined pituitary hormone deficiencies, genetic form
Disease Summary
Associated Targets (23)
Tbio
18
Tclin
4
Tchem
1
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
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0002252
GARD:0010602
OMIMPS:613038
Orphanet:95494
SCTID:718182008
MONDO:0013099
High level summary of knowledge for a disease, including descriptions and datasource references.