Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Ba1bbb726a37422af265a3c7effa1e3d2> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Ba1bbb726a37422af265a3c7effa1e3d2 hasDbXref "Orphanet:95494" @default.
- Ba1bbb726a37422af265a3c7effa1e3d2 type Axiom @default.
- Ba1bbb726a37422af265a3c7effa1e3d2 annotatedProperty IAO_0000115 @default.
- Ba1bbb726a37422af265a3c7effa1e3d2 annotatedSource MONDO_0013099 @default.
- Ba1bbb726a37422af265a3c7effa1e3d2 annotatedTarget "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." @default.